THE
HISTORY
OF
CHEMISTRY.
BY
THOMAS THOMSON, M. D.
F.R.S. L. & E.; F.L.S.; F.G.S., &c.
REGIUS PROFESSOR OF CHEMISTRY IN THE UNIVERSITY OF GLASGOW.
IN TWO VOLUMES.
VOL. II.
LONDON:
HENRY COLBURN AND RICHARD BENTLEY,
NEW BURLINGTON STREET.
1831.
C. WHITING, BEAUFORT HOUSE, STRAND.
CONTENTS
OF
THE SECOND VOLUME.
| [CHAPTER I]. | |
| Page | |
| Of the foundation and progress of scientific chemistry in Great Britain | 1 |
| [CHAPTER II]. | |
| Of the progress of philosophical chemistry in Sweden | 26 |
| [CHAPTER III]. | |
| Progress of scientific chemistry in France | 75 |
| [CHAPTER IV]. | |
| Progress of analytical chemistry | 190 |
| [CHAPTER V]. | |
| Of electro-chemistry | 251 |
| [CHAPTER VI]. | |
| Of the atomic theory | 277 |
| [CHAPTER VII]. | |
| Of the present state of chemistry | 309 |
HISTORY OF CHEMISTRY.
CHAPTER I.
OF THE FOUNDATION AND PROGRESS OF SCIENTIFIC CHEMISTRY IN GREAT BRITAIN.
While Mr. Cavendish was extending the bounds of pneumatic chemistry, with the caution and precision of a Newton, Dr. Priestley, who had entered on the same career, was proceeding with a degree of rapidity quite unexampled; while from his happy talents and inventive faculties, he contributed no less essentially to the progress of the science, and certainly more than any other British chemist to its popularity.
Joseph Priestley was born in 1733, at Fieldhead, about six miles from Leeds in Yorkshire. His father, Jonas Priestley, was a maker and dresser of woollen cloth, and his mother, the only child of Joseph Swift a farmer in the neighbourhood. Dr. Priestley was the eldest child; and, his mother having children very fast, he was soon committed to the care of his maternal grandfather. He lost his mother when he was only six years of age, and was soon after taken home by his father and sent to school in the neighbourhood. His father being but poor, and encumbered with a large family, his sister, Mrs. Keighley, a woman in good circumstances, and without children, relieved him of all care of his eldest son, by taking him and bringing him up as her own. She was a dissenter, and her house was the resort of all the dissenting clergy in the country. Young Joseph was sent to a public school in the neighbourhood, and, at sixteen, had made considerable progress in Latin, Greek, and Hebrew. Having shown a passion for books and for learning at a very early age, his aunt conceived hopes that he would one day become a dissenting clergyman, which she considered as the first of all professions; and he entered eagerly into her views: but his health declining about this period, and something like phthisical symptoms having come on, he was advised to turn his thoughts to trade, and to settle as a merchant in Lisbon. This induced him to apply to the modern languages; and he learned French, Italian, and German, without a master. Recovering his health, he abandoned his new scheme and resumed his former plan of becoming a clergyman. In 1752 he was sent to the academy of Daventry, to study under Dr. Ashworth, the successor of Dr. Doddridge. He had already made some progress in mechanical philosophy and metaphysics, and dipped into Chaldee, Syriac, and Arabic. At Daventry he spent three years, engaged keenly in studies connected with divinity, and wrote some of his earliest theological tracts. Freedom of discussion was admitted to its full extent in this academy. The two masters espoused different sides upon most controversial subjects, and the scholars were divided into two parties, nearly equally balanced. The discussions, however, were conducted with perfect good humour on both sides; and Dr. Priestley, as he tells us himself, usually supported the heterodox opinion; but he never at any time, as he assures us, advanced arguments which he did not believe to be good, or supported an opinion which he did not consider as true. When he left the academy, he settled at Needham in Suffolk, as an assistant in a small, obscure dissenting meeting-house, where his income never exceeded 30l. a-year. His hearers fell off, in consequence of their dislike of his theological opinions; and his income underwent a corresponding diminution. He attempted a school; but his scheme failed of success, owing to the bad opinion which his neighbours entertained of his orthodoxy. His situation would have been desperate, had he not been occasionally relieved by sums out of charitable funds, procured by means of Dr. Benson, and Dr. Kippis.
Several vacancies occurred in his vicinity; but he was treated with contempt, and thought unworthy to fill any of them. Even the dissenting clergy in the neighbourhood thought it a degradation to associate with him, and durst not ask him to preach: not from any dislike to his theological opinions; for several of them thought as freely as he did; but because the genteeler part of their audience always absented themselves when he appeared in the pulpit. A good many years afterwards, as he informs us himself, when his reputation was very high, he preached in the same place, and multitudes flocked to hear the very same sermons, which they had formerly listened to with contempt and dislike.
His friends being aware of the disagreeable nature of his situation at Needham, were upon the alert to procure him a better. In 1758, in consequence of the interest of Mr. Gill, he was invited to appear as a candidate for a meeting-house in Sheffield, vacant by the resignation of Mr. Wadsworth. He appeared accordingly and preached, but was not approved of. Mr. Haynes, the other minister, offered to procure him a meeting-house at Nantwich in Cheshire. This situation he accepted, and, to save expenses, he went from Needham to London by sea. At Nantwich he continued three years, and spent his time much more agreeably than he had done at Needham. His opinions were not obnoxious to his hearers, and controversial discussions were never introduced. Here he established a school, and found the business of teaching, contrary to his expectation, an agreeable and even interesting employment. He taught from seven in the morning, till four in the afternoon; and after the school was dismissed, he went to the house of Mr. Tomlinson, an eminent attorney in the neighbourhood, where he taught privately till seven in the evening. Being thus engaged twelve hours every day in teaching, he had little time for private study. It is, indeed, scarcely conceivable how, under such circumstances, he could prepare himself for Sunday. Here, however, his circumstances began to mend. At Needham it required the utmost economy to keep out of debt; but at Nantwich, he was able to purchase a few books and some philosophical instruments, as a small air-pump, an electrical machine, &c. These he taught his eldest scholars to keep in order and manage: and by entertaining their parents and friends with experiments, in which the scholars were generally the operators, and sometimes the lecturers too, he considerably extended the reputation of his school. It was at Nantwich that he wrote his grammar for the use of his school, a book of considerable merit, though its circulation was never extensive. This latter circumstance was probably owing to the superior reputation of Dr. Lowth, who published his well-known grammar about two years afterwards.
Being boarded in the house of Mr. Eddowes, a very sociable and sensible man, and a lover of music, Dr. Priestley was induced to play a little on the English flute; and though he never was a proficient, he informs us that it contributed more or less to his amusement for many years. He recommends the knowledge and practice of music to all studious persons, and thinks it rather an advantage for them if they have no fine ear or exquisite taste, as they will, in consequence, be more easily pleased, and less apt to be offended when the performances they hear are but indifferent.
The academy at Warrington was instituted while Dr. Priestley was at Needham, and he was recommended by Mr. Clark, Dr. Benson, and Dr. Taylor, as tutor in the languages; but Dr. Aiken, whose qualifications were considered as superior, was preferred before him. However, on the death of Dr. Taylor, and the advancement of Dr. Aiken to be tutor in divinity, he was invited to succeed him: this offer he accepted, though his school at Nantwich was likely to be more gainful; for the employment at Warrington was more liberal and less painful. In this situation he continued six years, actively employed in teaching and in literary pursuits. Here he wrote a variety of works, particularly his History of Electricity, which first brought him into notice as an experimental philosopher, and procured him celebrity. After the publication of this work, Dr. Percival of Manchester, then a student at Edinburgh, procured him the title of doctor in laws, from that university. Here he married a daughter of Mr. Isaac Wilkinson, an ironmonger in Wales; a woman whose qualities he has highly extolled, and who died after he went to America.
In the academy he spent his time very happily, but it did not flourish. A quarrel had broken out between Dr. Taylor and the trustees, in consequence of which all the friends of that gentleman were hostile to the institution. This, together with the smallness of his income, 100l. a-year, and 15l. for each boarder, which precluded him from making any provision for his family, induced him to accept an invitation to take charge of Millhill chapel, at Leeds, where he had a considerable acquaintance, and to which he removed in 1767.
Here he engaged keenly in the study of theology, and produced a great number of works, many of them controversial. Here, too, he commenced his great chemical career, and published his first tract on air. He was led accidentally to think of pneumatic chemistry, by living in the immediate vicinity of a brewery. Here, too, he published his history of the Discoveries relative to Light and Colours, as the first part of a general history of experimental philosophy; but the expense of this book was so great, and its sale so limited, that he did not venture to prosecute the undertaking. Here, likewise, he commenced and published three volumes of a periodical work, entitled "The Theological Repository," which he continued after he settled in Birmingham.
After he had been six years at Leeds, the Earl of Shelburne (afterwards Marquis of Lansdowne), engaged him, on the recommendation of Dr. Price, to live with him as a kind of librarian and literary companion, at a salary of 250l. a-year, with a house. With his lordship he travelled through Holland, France, and a part of Germany, and spent some time in Paris. He was delighted with this excursion, and expressed himself thoroughly convinced of the great advantages to be derived from foreign travel. The men of science and politicians in Paris were unbelievers, and even professed atheists, and as Dr. Priestley chose to appear before them as a Christian, they told him that he was the first person they had met with, of whose understanding they had any opinion, who was a believer of Christianity; but, upon interrogating them closely, he found that none of them had any knowledge either of the nature or principles of the Christian religion.—While with Lord Shelburne, he published the first three volumes of his Experiments on Air, and had collected materials for a fourth, which he published soon after settling in Birmingham. At this time also he published his attack upon Drs. Reid, Beattie, and Oswald; a book which, he tells us, he finished in a fortnight: but of which he afterwards, in some measure, disapproved. Indeed, it was impossible for any person of candour to approve of the style of that work, and the way in which he treated Dr. Reid, a philosopher certainly much more deeply skilled than himself in metaphysics.
After some years Lord Shelburne began to be weary of his associate, and, on his expressing a wish to settle him in Ireland, Dr. Priestley of his own accord proposed a separation, to which his lordship consented, after settling on him an annuity of 150l., according to a previous stipulation. This annuity he continued regularly to pay during the remainder of the life of Dr. Priestley.
His income being much diminished by his separation from Lord Shelburne, and his family increasing, he found it now difficult to support himself. At this time Mrs. Rayner made him very considerable presents, particularly at one period a sum of 400l.; and she continued her contributions to him almost annually. Dr. Fothergill had proposed a subscription, in order that he might prosecute his experiments to their utmost extent, and be enabled to live without sacrificing his time to his pupils. This he accepted. It amounted at first to 40l. per annum, and was afterwards much increased. Dr. Watson, Mr. Wedgewood, Mr. Galton, and four or five more, were the gentlemen who joined with Dr. Fothergill in this generous subscription.
Soon after, he settled in a meeting-house in Birmingham, and continued for several years engaged in theological and chemical investigations. His apparatus, by the liberality of his friends, had become excellent, and his income was so good that he could prosecute his researches to their full extent. Here he published the three last volumes of his Experiments on Air, and various papers on the same subject in the Philosophical Transactions. Here, too, he continued his Theological Repository, and published a variety of tracts on his peculiar opinions in religion, and upon the history of the primitive church. He now unluckily engaged in controversy with the established clergy of the place; and expressed his opinions on political subjects with a degree of freedom, which, though it would have been of no consequence at any former period, was ill suited to the peculiar circumstances that were introduced into this country by the French revolution, and to the political maxims of Mr. Pitt and his administration. His answer to Mr. Burke's book on the French revolution excited the violent indignation of that extraordinary man, who inveighed against his character repeatedly, and with peculiar virulence, in the house of commons. The clergy of the church of England, too, who began about this time to be alarmed for their establishment, of which Dr. Priestley was the open enemy, were particularly active; the press teemed with their productions against him, and the minds of their hearers seem to have been artificially excited; indeed some of the anecdotes told of the conduct of the clergy of Birmingham, were highly unbecoming their character. Unfortunately, Dr. Priestley did not seem to be aware of the state of the nation, and of the plan of conduct laid down by Mr. Pitt and his political friends; and he was too fond of controversial discussions to yield tamely to the attacks of his antagonists.
These circumstances seem in some measure to explain the disgraceful riots which took place in Birmingham in 1791, on the day of the anniversary of the French revolution. Dr. Priestley's meeting-house and his dwelling-house were burnt; his library and apparatus destroyed, and many manuscripts, the fruits of several years of industry, were consumed in the conflagration. The houses of several of his friends shared the same fate, and his son narrowly escaped death, by the care of a friend who forcibly concealed him for several days. Dr. Priestley was obliged to make his escape to London, and a seat was taken for him in the mail-coach under a borrowed name. Such was the ferment against him that it was believed he would not have been safe any where else; and his friends would not allow him, for several weeks, to walk through the streets.
He was invited to Hackney, to succeed Dr. Price in the meeting-house of that place. He accepted the office, but such was the dread of his unpopularity, that nobody would let him a house, from an apprehension that it would be burnt by the populace as soon as it was known that he inhabited it. He was obliged to get a friend to take a lease of a house in another name; and it was with the utmost difficulty that he could prevail with the landlord to allow the lease to be transferred to him. The members of the Royal Society, of which he was a fellow, declined admitting him into their company; and he was obliged to withdraw his name from the society.
When we look back upon this treatment of a man of Dr. Priestley's character, after an interval of forty years, it cannot fail to strike us with astonishment; and it must be owned, I think, that it reflects an indelible stain upon that period of the history of Great Britain. To suppose that he was in the least degree formidable to so powerful a body as the church of England, backed as it was by the aristocracy, by the ministry, and by the opinions of the people, is perfectly ridiculous. His theological sentiments, indeed, were very different from those of the established church; but so were those of Milton, Locke, and Newton. Nay, some of the members of the church itself entertained opinions, not indeed so decided or so openly expressed as those of Dr. Priestley, but certainly having the same tendency. To be satisfied of this it is only necessary to recollect the book which Dr. Clarke published on the Trinity. Nay, some of the bishops, unless they are very much belied, entertained opinions similar to those of Dr. Clarke. The same observation applies to Dr. Lardner, Dr. Price, and many others of the dissenters. Yet, the church of England never attempted to persecute these respectable and meritorious men, nor did they consider their opinions as at all likely to endanger the stability of the church. Besides, Dr. Horsley had taken up the pen against Dr. Priestley's theological opinions, and had refuted them so completely in the opinion of the members of the church, that it was thought right to reward his meritorious services by a bishopric.
It could hardly, therefore, be the dread of Dr. Priestley's theological opinions that induced the clergy of the church of England to bestir themselves against him with such alacrity. Erroneous opinions advanced and refuted, so far from being injurious, have a powerful tendency to support and strengthen the cause which they were meant to overturn. Or, if there existed any latent suspicion that the refutation of Horsley was not so complete as had been alleged, surely persecution was not the best means of supporting weak arguments; and indeed it was rather calculated to draw the attention of mankind to the theological opinions of Priestley; as has in fact been the consequence.
Neither can the persecutions which Dr. Priestley was subjected to be accounted for by his political opinions, even supposing it not to be true, that in a free country like Great Britain, any man is at liberty to maintain whatever theoretic opinions of government he thinks proper, provided he be a peaceable subject and obey rigorously all the laws of his country.
Dr. Priestley was an advocate for the perfectibility of the human species, or at least its continually increasing tendency to improvement—a doctrine extremely pleasing in itself, and warmly supported by Franklin and Price; but which the wild principles of Condorcet, Godwin, and Beddoes at last brought into discredit. This doctrine was taught by Priestley in the outset of his Treatise on Civil Government, first published in 1768. It is a speculation of so very agreeable a nature, so congenial to our warmest wishes, and so flattering to the prejudices of humanity, that one feels much pain at being obliged to give it up. Perhaps it may be true, and I am willing to hope so, that improvements once made are never entirely lost, unless they are superseded by something much more advantageous, and that therefore the knowledge of the human race, upon the whole, is progressive. But political establishments, at least if we are to judge from the past history of mankind, have their uniform periods of progress and decay. Nations seem incapable of profiting by experience. Every nation seems destined to run the same career, and the history may be comprehended under the following heads: Poverty, liberty, industry, wealth, power, dissipation, anarchy, destruction. We have no example in history of a nation running through this career and again recovering its energy and importance. Greece ran through it more than two thousand years ago: she has been in a state of slavery ever since. An opportunity is now at last given her of recovering her importance: posterity will ascertain whether she will embrace it.
Dr. Priestley's short Essay on the First Principles of Civil Government was published in 1768. In it he lays down as the foundation of his reasoning, that "it must be understood, whether it be expressed or not, that all people live in society for their mutual advantage; so that the good and happiness of the members, that is the majority of the members of any state, is the great standard by which every thing relating to that state must be finally determined; and though it may be supposed that a body of people may be bound by a voluntary resignation of all their rights to a single person or to a few, it can never be supposed that the resignation is obligatory on their posterity, because it is manifestly contrary to the good of the whole that it should be so." From this first principle he deduces all his political maxims. Kings, senators, and nobles, are merely the servants of the public; and when they abuse their power, in the people lies the right of deposing and consequently of punishing them. He examines the expediency of hereditary sovereignty, of hereditary rank and privileges, of the duration of parliament, and of the right of voting, with an evident tendency to democratical principles, though he does not express himself very clearly on the subject.
Such were his political principles in 1768, when his book was published. They excited no alarm and drew but little attention; these principles he maintained ever after, or indeed he may be said to have become more moderate instead of violent. Though he approved of a republic in the abstract; yet, considering the prejudices and habits of the people of Great Britain, he laid it down as a principle that their present form of government was best suited to them. He thought, however, that there should be a reform in parliament; and that parliaments should be triennial instead of septennial. He was an enemy to all violent reforms, and thought that the change ought to be brought about gradually and peaceably. When the French revolution broke out he took the side of the patriots, as he had done during the American war; and he wrote a refutation of Mr. Burke's extraordinary performance. Being a dissenter, it is needless to say that he was an advocate for complete religious freedom. He was ever hostile to all religious establishments, and an open enemy to the church of England.
How far these opinions were just and right this is not the place to inquire; but that they were perfectly harmless, and that many other persons in this country during the last century, and even at present, have adopted similar opinions without incurring any odium whatever, and without exciting the jealousy or even the attention of government, is well known to every person. It comes then to be a question of some curiosity at least, to what we are to ascribe the violent persecutions raised against Dr. Priestley. It seems to have been owing chiefly to the alarm caught by the clergy of the established church that their establishment was in danger;—and, considering the ferment excited soon after the breaking out of the French revolution, and the rage for reform, which pervaded all ranks, the almost general alarm of the aristocracy, at least, was not entirely without foundation. I cannot, however, admit that there was occasion for the violent alarm caught by Mr. Pitt and his political friends, and for the very despotic measures which they adopted in consequence. The disease would probably have subsided of itself, or it would have been cured by a much gentler treatment. As Dr. Priestley was an open enemy to the establishment, its clergy naturally conceived a prejudice against him, and this prejudice was violently inflamed by the danger to which they thought themselves exposed; their influence with the ministry was very great, and Mr. Pitt and his friends naturally caught their prejudices and opinions. Mr. Burke, too, who had changed his political principles, and who was inflamed with the burning zeal which distinguishes all converts, was provoked at Dr. Priestley's answer to his book on the French revolution, and took every opportunity to inveigh against him in the house of commons. The conduct of the French, likewise, who made Dr. Priestley a citizen of France, and chose him a member of their assembly, though intended as a compliment, was injurious to him in Great Britain. It was laid hold of by his antagonists to convince the people that he was an enemy to his country; that he had abjured his rights as an Englishman; and that he had adopted the principles of the hereditary enemies of Great Britain. These causes, and not his political opinions, appear to me to account for the persecution which was raised against him.
His sons, disgusted with this persecution of their father, had renounced their native country and gone over to France; and, on the breaking out of the war between this country and the French republic, they emigrated to America. It was this circumstance, joined to the state of insulation in which he lived, that induced Dr. Priestley, after much consideration, to form the resolution of following his sons and emigrating to America. He published his reasons in the preface to a Fast-day Sermon, printed in 1794, one of the gravest and most forcible pieces of composition I have ever read. He left England in April, 1795, and reached New York in June. In America he was received with much respect by persons of all ranks; and was immediately offered the situation of professor of chemistry in the College of Philadelphia; which, however, he declined, as his circumstances, by the liberality of his friends in England, continued independent. He settled, finally, in Northumberland, about 130 miles from Philadelphia, where he built a house, and re-established his library and laboratory, as well as circumstances permitted. Here he published a considerable number of chemical papers, some of them under the form of pamphlets, and the rest in the American Transactions, the New York Medical Repository, and Nicholson's Journal of Natural Philosophy and Chemistry. Here, also, he continued keenly engaged in theological pursuits; and published, or republished, a great variety of books on theological subjects. Here he lost his wife and his youngest and favourite son, who, he had flattered himself, was to succeed him in his literary career:—and here he died, in 1804, after having been confined only two days to bed, and but a few hours after having arranged his literary concerns, inspected some proof-sheets of his last theological work, and given instructions to his son how it should be printed.
During the latter end of the presidency of Mr. Adams, the same kind of odium which had banished Dr. Priestley from England began to prevail in America. He was threatened with being sent out of the country as an alien. Notwithstanding this, he declined being naturalized; resolving, as he said, to die as he had lived, an Englishman. When his friend Mr. Jefferson, whose political opinions coincided with his own, became president, the odium against him wore off, and he became as much respected as ever.
As to the character of Dr. Priestley, it is so well marked by his life and writings, that it is difficult to conceive how it could have been mistaken by many eminent men in this kingdom. Industry was his great characteristic; and this quality, together with a facility of composition, acquired, as he tells us, by a constant habit while young of drawing out an abstract of the sermons which he had preached, and writing a good deal in verse, enabled him to do so much: yet, he informs us that he never was an intense student, and that his evenings were usually passed in amusement or company. He was an early riser, and always lighted his own fire before any one else was stirring: it was then that he composed all his works. It is obvious, from merely glancing into his books, that he was precipitate; and indeed, from the way he went on thinking as he wrote, and writing only one copy, it was impossible he could be otherwise: but, as he was perfectly sincere and anxious to obtain the truth, he freely acknowledged his mistakes as soon as he became sensible of them. This candour is very visible in his philosophical speculations; but in his theological writings it was not so much to be expected. He was generally engaged in controversy in theology; and his antagonists were often insolent, and almost always angry. We all know the effect of such opposition; and need not be surprised that it operated upon Dr. Priestley, as it would do upon any other man. By all accounts his powers of conversation were very great, and his manners in every respect very agreeable. That this must have been the case is obvious from the great number of his friends, and the zeal and ardour with which they continued to serve him, notwithstanding the obloquy under which he lay, and even the danger that might be incurred by appearing to befriend him. As for his moral character, even his worst enemies have been obliged to allow that it was unexceptionable. Many of my readers will perhaps smile, when I say that he was not only a sincere, but a zealous Christian, and would willingly have died a martyr to the cause. Yet I think the fact is of easy proof; and his conduct through life, and especially at his death, affords irrefragable proofs of it. His tenets, indeed, did not coincide with those of the majority of his countrymen; but though he rejected many of the doctrines, he admitted the whole of the sublime morality and the divine origin of the Christian religion; which may charitably be deemed sufficient to constitute a true Christian. Of vanity he seems to have possessed rather more than a usual share; but perhaps he was deficient in pride.
His writings were exceedingly numerous, and treated of science, theology, metaphysics, and politics. Of his theological, metaphysical, and political writings it is not our business in this work to take any notice. His scientific works treat of electricity, optics, and chemistry. As an electrician he was respectable; as an optician, a compiler; as a chemist, a discoverer. He wrote also a book on perspective which I have never had an opportunity of perusing.
It is to his chemical labours that he is chiefly indebted for the great reputation which he acquired. No man ever entered upon any undertaking with less apparent means of success than Dr. Priestley did on the chemical investigation of airs. He was unacquainted with chemistry, excepting that he had, some years before, attended an elementary course delivered by Mr. Turner, of Liverpool. He was not in possession of any apparatus, nor acquainted with the method of making chemical experiments; and his circumstances were such, that he could neither lay out a great deal of money on experiments, nor could he hope, without a great deal of expense, to make any material progress in his investigations. These circumstances, which, at first sight, seem so adverse, were, I believe, of considerable service to him, and contributed very much to his ultimate success. The branch of chemistry which he selected was new: an apparatus was to be invented before any thing of importance could be effected; and, as simplicity is essential in every apparatus, he was most likely to contrive the best, whose circumstances obliged him to attend to economical considerations.
Pneumatic chemistry had been begun by Mr. Cavendish in his valuable paper on carbonic acid and hydrogen gases, published in the Philosophical Transactions for 1766. The apparatus which he employed was similar to that used about a century before by Dr. Mayow of Oxford. Dr. Priestley contrived the apparatus still used by chemists in pneumatic investigations; it is greatly superior to that of Mr. Cavendish, and, indeed, as convenient as can be desired. Were we indebted to him for nothing else than this apparatus, it would deservedly give him high consideration as a pneumatic chemist.
His discoveries in pneumatic chemistry are so numerous, that I must satisfy myself with a bare outline; to enumerate every thing, would be to transcribe his three volumes, into which he digested his discoveries. His first paper was published in 1772, and was on the method of impregnating water with carbonic acid gas; the experiments contained in it were the consequence of his residing near a brewery in Leeds. This pamphlet was immediately translated into French; and, at a meeting of the College of Physicians in London, they addressed the Lords of the Treasury, pointing out the advantage that might result from water impregnated with carbonic acid gas in cases of scurvy at sea. His next essay was published in the Philosophical Transactions, and procured him the Copleyan medal. His different volumes on air were published in succession, while he lived with Lord Shelburne, and while he was settled at Birmingham. They drew the attention of all Europe, and raised the reputation of this country to a great height.
The first of his discoveries was nitrous gas, now called deutoxide of azote, which had, indeed, been formed by Dr. Hales; but that philosopher had not attempted to investigate its properties. Dr. Priestley ascertained its properties with much sagacity, and almost immediately applied it to the analysis of air. It contributed very much to all subsequent investigations in pneumatic chemistry, and may be said to have led to our present knowledge of the constitution of the atmosphere.
The next great discovery was oxygen gas, which was made by him on the 1st of August, 1774, by heating the red oxide of mercury, and collecting the gaseous matter given out by it. He almost immediately detected the remarkable property which this gas has of supporting combustion better, and animal life longer, than the same volume of common air; and likewise the property which it has of condensing into red fumes when mixed with nitrous gas. Lavoisier, likewise, laid claim to the discovery of oxygen gas; but his claim is entitled to no attention whatever; as Dr. Priestley informs us that he prepared this gas in M. Lavoisier's house, in Paris, and showed him the method of procuring it in the year 1774, which is a considerable time before the date assigned by Lavoisier for his pretended discovery. Scheele, however, actually obtained this gas without any previous knowledge of what Priestley had done; but the book containing this discovery was not published till three years after Priestley's process had become known to the public.
Dr. Priestley first made known sulphurous acid, fluosilicic acid, muriatic acid, and ammonia in the gaseous form; and pointed out easy methods of procuring them: he describes with exactness the most remarkable properties of each. He likewise pointed out the existence of carburetted hydrogen gas; though he made but few experiments to determine its nature. His discovery of protoxide of azote affords a beautiful example of the advantages resulting from his method of investigation, and the sagacity which enabled him to follow out any remarkable appearances which occurred. Carbonic oxide gas was discovered by him while in America, and it was brought forward by him as an incontrovertible refutation of the antiphlogistic theory.
Though he was not strictly the discoverer of hydrogen gas, yet his experiments on it were highly interesting, and contributed essentially to the revolution which chemistry soon after underwent. Nothing, for example, could be more striking, than the reduction of oxide of iron, and the disappearance of the hydrogen when the oxide is heated sufficiently in contact with hydrogen gas. Azotic gas was known before he began his career; but we are indebted to him for most of the properties of it yet known. To him, also, we owe the knowledge of the fact, that an acid is formed when electric sparks are made to pass for some time through a given bulk of common air; a fact which led afterwards to Mr. Cavendish's great discovery of the composition of nitric acid.
He first discovered the great increase of bulk which takes place when electric sparks are made to pass through ammoniacal gas—a fact which led Berthollet to the analysis of this gas. He merely repeated Priestley's experiment, determined the augmentation of bulk, and the nature of the gases evolved by the action of the electricity. His experiments on the amelioration of atmospherical air by the vegetation of plants, on the oxygen gas given out by their leaves, and on the respiration of animals, are not less curious and interesting.
Such is a short view of the most material facts for which chemistry is indebted to Dr. Priestley. As a discoverer of new substances, his name must always stand very high in the science; but as a reasoner or theorist his position will not be so favourable. It will be observed that almost all his researches and discoveries related to gaseous bodies. He determined the different processes, by means of which the different gases can be procured, the substances which yield them, and the effects which they are capable of producing on other bodies. Of the other departments of chemistry he could hardly be said to know any thing. As a pneumatic chemist he stands high; as an analytical chemist he can scarcely claim any rank whatever. In his famous experiments on the formation of water by detonating mixtures of oxygen and hydrogen in a copper globe, the copper was found acted upon, and a blue liquid was obtained, the nature of which he was unable to ascertain; but Mr. Keir, whose assistance he solicited, determined it to be a solution of nitrate of copper in water. This formation of nitric acid induced him to deny that water was a compound of oxygen and hydrogen. The same acid was formed in the experiments of Mr. Cavendish; but he investigated the circumstances of the formation, and showed that it depended upon the presence of azotic gas in the gaseous mixture. Whenever azotic gas is present, nitric acid is formed, and the quantity of this acid depends upon the relative proportion of the azotic and hydrogen gases in the mixture. When no hydrogen gas is present, nothing is formed but nitric acid: when no azotic gas is present, nothing is formed but water. These facts, determined by Cavendish, invalidate the reasoning of Priestley altogether; and had he possessed the skill, like Cavendish, to determine with sufficient accuracy the proportions of the different gases in his mixtures, and the relative quantities of nitric acid formed, he would have seen the inaccuracy of his own conclusions.
He was a firm believer in the existence of phlogiston; but he seems, at least ultimately, to have adopted the view of Scheele, and many other eminent contemporary chemists—indeed, the view of Cavendish himself—that hydrogen gas is phlogiston in a separate and pure state. Common air he considered as a compound of oxygen and phlogiston. Oxygen, in his opinion, was air quite free from phlogiston, or air in a simple and pure state; while azotic gas (the other constituent of common air) was air saturated with phlogiston. Hence he called oxygen dephlogisticated, and azote phlogisticated air. The facts that when common air is converted into azotic gas its bulk is diminished about one-fifth part, and that azotic gas is lighter than common air or oxygen gas, though not quite unknown to him, do not seem to have drawn much of his attention. He was not accustomed to use a balance in his experiments, nor to attend much to the alterations which took place in the weight of bodies. Had he done so, most of his theoretical opinions would have fallen to the ground.
When a body is allowed to burn in a given quantity of common air, it is known that the quality of the common air is deteriorated; it becomes, in his language, more phlogisticated. This, in his opinion, was owing to an affinity which existed between phlogiston and air. The presence of air is necessary to combustion, in consequence of the affinity which it has for phlogiston. It draws phlogiston out of the burning body, in order to combine with it. When a given bulk of air is saturated with phlogiston, it is converted into azotic gas, or phlogisticated air, as he called it; and this air, having no longer any affinity for phlogiston, can no longer attract that principle, and consequently combustion cannot go on in such air.
All combustible bodies, in his opinion, contain hydrogen. Of course the metals contain it as a constituent. The calces of metals are those bodies deprived of phlogiston. To prove the truth of this opinion, he showed that when the oxide of iron is heated in hydrogen gas, that gas is absorbed, while the calx is reduced to the metallic state. Finery cinder, which he employed in these experiments, is, in his opinion, iron not quite free from phlogiston. Hence it still retains a quantity of hydrogen. To prove this, he mixed together finery cinder and carbonates of lime, barytes and strontian, and exposed the mixture to a strong heat; and by this process obtained inflammable gas in abundance. In his opinion every inflammable gas contains hydrogen in abundance. Hence this experiment was adduced by him as a demonstration that hydrogen is a constituent of finery cinder.
All these processes of reasoning, which appear so plausible as Dr. Priestley states them, vanish into nothing, when his experiments are made, and the weights of every thing determined by means of a balance: it is then established that a burning body becomes heavier during its combustion, and that the surrounding air loses just as much weight as the burning body gains. Scheele and Lavoisier showed clearly that the loss of weight sustained by the air is owing to a quantity of oxygen absorbed from it, and condensed in the burning body. Cruikshank first elucidated the nature of the inflammable gas, produced by the heating a mixture of finery cinder and carbonate of lime, or other earthy carbonate. He found that iron filings would answer better than finery cinder. The gas was found to contain no hydrogen, and to be in fact a compound of oxygen and carbon. It was shown to be derived from the carbonic acid of the earthy carbonate, which was deprived of half its oxygen by the iron filings or finery cinder. Thus altered, it no longer preserved its affinity for the lime, but made its escape in the gaseous form, constituting the gas now known by the name of carbonic oxide.
Though the consequence of the Birmingham riots, which obliged Dr. Priestley to leave England and repair to America, is deeply to be lamented, as fixing an indelible disgrace upon the country; perhaps it was not in reality so injurious to Dr. Priestley as may at first sight appear. He had carried his peculiar researches nearly as far as they could go. To arrange and methodize, and deduce from them the legitimate consequences, required the application of a different branch of chemical science, which he had not cultivated, and which his characteristic rapidity, and the time of life to which he had arrived, would have rendered it almost impossible for him to acquire. In all probability, therefore, had he been allowed to prosecute his researches unmolested, his reputation, instead of an increase, might have suffered a diminution, and he might have lost that eminent situation as a man of science which he had so long occupied.
With Dr. Priestley closes this period of the History of British Chemistry—for Mr. Cavendish, though he had not lost his activity, had abandoned that branch of science, and turned his attention to other pursuits.
CHAPTER II.
OF THE PROGRESS OF PHILOSOPHICAL CHEMISTRY IN SWEDEN.
Though Sweden, partly in consequence of her scanty population, and the consequent limited sale of books in that country, and partly from the propensity of her writers to imitate the French, which has prevented that originality in her poets and historians that is requisite for acquiring much eminence—though Sweden, for these reasons, has never reached a very high rank in literature; yet the case has been very different in science. She has produced men of the very first eminence, and has contributed more than her full share in almost every department of science, and in none has she shone with greater lustre than in the department of Chemistry. Even in the latter part of the seventeenth century, before chemistry had, properly speaking, assumed the rank of a science, we find Hierne in Sweden, whose name deserves to be mentioned with respect. Moreover, in the earlier part of the eighteenth century, Brandt, Scheffer, and Wallerius, had distinguished themselves by their writings. Cronstedt, about the middle of the eighteenth century, may be said to have laid the foundation of systematic mineralogy upon chemical principles, by the publication of his System of Mineralogy. But Bergman is entitled to the merit of being the first person who prosecuted chemistry in Sweden on truly philosophical principles, and raised it to that high estimation to which its importance justly entitles it.
Torbern Bergman was born at Catherinberg, in West Gothland, on the 20th of March, 1735. His father, Barthold Bergman, was receiver of the revenues of that district, and his mother, Sara Hägg, the daughter of a Gotheborg merchant. A receiver of the revenues was at that time, in Sweden, a post both disagreeable and hazardous. The creatures of a party which had had the ascendancy in one diet, they were exposed to the persecution of the diet next following, in which an opposite party usually had the predominance. This circumstance induced Bergman to advise his son to turn his attention to the professions of law or divinity, which were at that time the most lucrative in Sweden. After having spent the usual time at school, and acquired those branches of learning commonly taught in Sweden, in the public schools and academies to which Bergman was sent, he went to the University of Upsala, in the autumn of 1752, where he was placed under the guidance of a relation, whose province it was to superintend his studies, and direct them to those pursuits that were likely to lead young Bergman to wealth and distinction. Our young student showed at once a decided predilection for mathematics, and those branches of physics which were connected with mathematics, or depended upon them. But these were precisely the branches of study which his relation was anxious to prevent his indulging in. Bergman attempted at once to indulge his own inclination, and to gratify the wishes of his relation. This obliged him to study with a degree of ardour and perseverance which has few examples. His mathematical and physical studies claimed the first share of his attention; and, after having made such progress in them as would alone have been sufficient to occupy the whole time of an ordinary student—to satisfy his relation, Jonas Victorin, who was at that time a magister docens in Upsala, he thought it requisite to study some law books besides, that he might be able to show that he had not neglected his advice, nor abandoned the views which he had held out.
He was in the habit of rising to his studies every morning at four o'clock, and he never went to bed till eleven at night. The first year of his residence at Upsala, he had made himself master of Wolf's Logic, of Wallerius's System of Chemistry, and of twelve books of Euclid's Elements: for he had already studied the first book of that work in the Gymnasium before he went to college. He likewise perused Keil's Lectures on Astronomy, which at that time were considered as the best introduction to physics and astronomy. His relative disapproved of his mathematical and physical studies altogether; but, not being able to put a stop to them, he interdicted the books, and left his young charge merely the choice between law and divinity. Bergman got a small box made, with a drawer, into which he put his mathematical and physical books, and over this box he piled the law books which his relative had urged him to study. At the time of the daily visits of his relative, the mathematical and physical books were carefully locked up in the drawer, and the law books spread upon the table; but no sooner was his presence removed, than the drawer was opened, and the mathematical studies resumed.
This incessant study; this necessity under which he found himself to consult his own inclinations and those of his relative; this double portion of labour, without time for relaxation, exercise, or amusement, proved at last injurious to young Bergman's health. He fell ill, and was obliged to leave the university and return home to his father's house in a state of bad health. There constant and moderate exercise was prescribed him, as the only means of restoring his health. That his time here might not be altogether lost to him, he formed the plan of making his walks subservient to the study of botany and entomology.
At this time Linnæus, after having surmounted obstacles which would have crushed a man of ordinary energy, was in the height of his glory; and was professor of botany and natural history in the University of Upsala. His lectures were attended by crowds of students from every country in Europe: he was enthusiastically admired and adored by his students. This influence on the minds of his pupils was almost unbounded; and at Upsala, every student was a natural historian. Bergman had studied botany before he went to college, and he had acquired a taste for entomology from the lectures of Linnæus himself. Both of these pursuits he continued to follow after his return home to West Gothland; and he made a collection of plants and of insects. Grasses and mosses were the plants to which he turned the most of his attention, and of which he collected the greatest number. But he felt a predilection for the study of insects, which was a field much less explored than the study of plants.
Among the insects which he collected were several not to be found in the Fauna Suecica. Of these he sent specimens to Linnæus at Upsala, who was delighted with the present. All of them were till then unknown as Swedish insects, and several of them were quite new. The following were the insects at this time collected by Bergman, and sent to Upsala, as they were named by Linnæus:
| Phalæna. | Bombyx monacha, camelina. |
| Noctua Parthenias, conspicillaris. | |
| Perspicillaris, flavicornis, Plebeia. | |
| Geometra pennaria. | |
| Tortrix Bergmanniana, Lediana. | |
| Tinea Harrisella, Pedella, Punctella. | |
| Tenthredo. | Vitellina, ustulata. |
| Ichneumon. | Jaculator niger. |
| Tipula. | Tremula. |
When Bergman's health was re-established, he returned to Upsala with full liberty to prosecute his studies according to his own wishes, and to devote the whole of his time to mathematics, physics, and natural history. His relations, finding it in vain to combat his predilections for these studies, thought it better to allow him to indulge them.
He had made himself known to Linnæus by the collection of insects which he had sent him from Catherinberg; and, drawn along by the glory with which Linnæus was surrounded, and the zeal with which his fellow-students prosecuted such studies, he devoted a great deal of his attention to natural history. The first paper which he wrote upon the subject contained a discovery. There was a substance observed in some ponds not far from Upsala, to which the name of coccus aquaticus was given, but its nature was unknown. Linnæus had conjectured that it might be the ovarium of some insect; but he left the point to be determined by future observations. Bergman ascertained that it was the ovum of a species of leech, and that it contained from ten to twelve young animals. When he stated what he had ascertained to Linnæus, that great naturalist refused to believe it; but Bergman satisfied him of the truth of his discovery by actual observation. Linnæus, thus satisfied, wrote under the paper of Bergman, Vidi et obstupui, and sent it to the academy of Stockholm with this flattering panegyric. It was printed in the Memoirs of that learned body for 1756 (p. 199), and was the first paper of Bergman's that was committed to the press.
He continued to prosecute the study of natural history as an amusement; though mathematics and natural philosophy occupied by far the greatest part of his time. Various useful papers of his, connected with entomology, appeared from time to time in the Memoirs of the Stockholm Academy; in particular, a paper on the history of insects which attack fruit-trees, and on the methods of guarding against their ravages: on the method of classing these insects from the forms of their larvæ, a time when it would be most useful for the agriculturist to know, in order to destroy those that are hurtful: a great number of observations on this class of animals, so various in their shape and their organization, and so important for man to know—some of which he has been able to overcome, while others, defended by their small size, and powerful by their vast numbers, still continue their ravages; and which offer so interesting a sight to the philosopher by their labours, their manners, and their foresight.—Bergman was fond of these pursuits, and looked back upon them in afterlife with pleasure. Long after, he used to mention with much satisfaction, that by the use of the method pointed out by him, no fewer than seven millions of destructive insects were destroyed in a single garden, and during the course of a single summer.
About the year 1757 he was appointed tutor to the only son of Count Adolf Frederick Stackelberg, a situation which he filled greatly to the satisfaction both of the father and son, as long as the young count stood in need of an instructor. He took his master's degree in 1758, choosing for the subject of his thesis on astronomical interpolation. Soon after, he was appointed magister docens in natural philosophy, a situation peculiar to the University of Upsala, and constituting a kind of assistant to the professor. For his promotion to this situation he was obliged to M. Ferner, who saw how well qualified he was for it, and how beneficial his labours would be to the University of Upsala. In 1761 he was appointed adjunct in mathematics and physics, which, I presume, means that he was raised to the rank of an associate with the professor of these branches of science. In this situation it was his business to teach these sciences to the students of Upsala, a task for which he was exceedingly well fitted. During this period he published various tracts on different branches of physical science, particularly on the rainbow, the crepuscula, the aurora-borealis, the electrical phenomena of Iceland spar, and of the tourmalin. We find his name among the astronomers who observed the first transit of Venus over the sun, in 1761, whose results deserve the greatest confidence.[1] His observations on the electricity of the tourmalin are important. It was he that first established the true laws that regulate these curious phenomena.
During the whole of this period he had been silently studying chemistry and mineralogy, though nobody suspected that he was engaged in any such pursuits. But in 1767 John Gottschalk Wallerius, who had long filled the chair of chemistry in the University of Upsala, with high reputation, resigned his chair. Bergman immediately offered himself as a candidate for the vacant professorship: and, to show that he was qualified for the office, published two dissertations on the Manufacture of Alum, which probably he had previously drawn up, and had lying by him. Wallerius intended to resign his chair in favour of a pupil or relation of his own, whom he had destined to succeed him. He immediately formed a party to oppose the pretensions of Bergman; and his party was so powerful and so malignant, that few doubted of their success: for it was joined by all those who, despairing of equalling the industry and reputation of Bergman, set themselves to oppose and obstruct his success. Such men unhappily exist in all colleges, and the more eminent a professor is, the more is he exposed to their malignant activity. Many of those who cannot themselves rise to any eminence, derive pleasure from the attempt to pull down the eminent to their own level. In these attempts, however, they seldom succeed, unless from some want of prudence and steadiness in the individual whom they assail. Bergman's Dissertations on Alum were severely handled by Wallerius and his party: and such was the influence of the ex-professor, that every body thought Bergman would be crushed by him.
Fortunately, Gustavus III. of Sweden, at that time crown prince, was chancellor of the university. He took up the cause of Bergman, influenced, it is said, by the recommendation of Von Swab, who pledged himself for his qualifications, and was so keen on the subject that he pleaded his cause in person before the senate. Wallerius and his party were of course baffled, and Bergman got the chair.
For this situation his previous studies had fitted him in a peculiar manner. His mathematical, physical, and natural-historical knowledge, so far from being useless, contributed to free him from prejudices, and to emancipate him from that spirit of routine under which chemistry had hitherto suffered. They gave to his ideas a greater degree of precision, and made his views more correct. He saw that mathematics and chemistry divided between them the whole extent of natural science, and that its bounds required to be enlarged, to enable it to embrace all the different branches of science with which it was naturally connected, or which depended upon it. He saw the necessity of banishing from chemistry all vague hypotheses and explanations, and of establishing the science on the firm basis of experiment. He was equally convinced of the necessity of reforming the nomenclature of chemistry, and of bringing it to the same degree of precision that characterized the language of the other branches of natural philosophy.
His first care, after getting the chair, was to make as complete a collection as he could of mineral substances, and to arrange them in order according to the nature of their constituents, as far as they had been determined by experiment. To another cabinet he assigned the Swedish minerals, ranged in a geographical manner according to the different provinces which furnished them.
When I was at Upsala, in 1812, the first of these collections still remained, greatly augmented by his nephew and successor, Afzelius. But no remains existed of the geographical collection. However, there was a very considerable collection of this kind in the apartments of the Swedish school of mines at Stockholm, under the care of Mr. Hjelm, which I had an opportunity of inspecting. It is not improbable that Bergman's collection might have formed the nucleus of this. A geographical collection of minerals, to be of much utility, should exhibit all the different formations which exist in the kingdom: and in a country so uniform in its nature as Sweden, the minerals of one county are very nearly similar to those of the other counties; with the exception of certain peculiarities derived from the mines, or from some formations which may belong exclusively to certain parts of the country, as, for example, the coal formations in the south corner of Sweden, near Helsinburg, and the porphyry rocks, in Elfsdale.
Bergman attempted also to make a collection of models of the apparatus employed in the different chemical manufactories, to be enabled to explain these manufactures with greater clearness to his students. I was informed by M. Ekeberg, who, in 1812, was magister docens in chemistry at Upsala, that these models were never numerous. Nor is it likely that they should be, as Sweden cannot boast of any great number of chemical manufactories, and as, in Bergman's time, the processes followed in most of the chemical manufactories of Europe were kept as secret as possible.
Thus it was Bergman's object to exhibit to his pupils specimens of all the different substances which the earth furnishes, with the order in which these productions are arranged on the globe—to show them the uses made of all these different productions—how practice had preceded theory and had succeeded in solving many chemical problems of the most complicated nature.
His lectures are said to have been particularly valuable. He drew around him a considerable number of pupils, who afterwards figured as chemical discoverers themselves. Of all these Assessor Gahn, of Fahlun, was undoubtedly the most remarkable; but Hjelm, Gadolin, the Elhuyarts, and various other individuals, likewise distinguished themselves as chemists.
After his appointment to the chemical chair at Upsala, the remainder of his life passed with very little variety; his whole time was occupied with his favourite studies, and not a year passed that he did not publish some dissertation or other upon some more or less important branch of chemistry. His reputation gradually extended itself over Europe, and he was enrolled among the number of the members of most scientific academies. Among other honourable testimonies of the esteem in which he was held, he was elected rector of the University of Upsala. This university is not merely a literary body, but owns extensive estates, over which it possesses great authority, and, having considerable control over its students, and enjoying considerable immunities and privileges (conferred in former times as an encouragement to learning, though, in reality, they serve only to cramp its energies, and throw barriers in the way of its progress), constitutes, therefore, a kind of republic in the midst of Sweden: the professors being its chiefs. But while, in literary establishments, all the institutions ought to have for an object to maintain peace, and free their members from every occupation unconnected with letters, the constitution of that university obliges its professors to attend to things very inconsistent with their usual functions; while it gives men of influence and ambition a desire to possess the power and patronage, though they may not be qualified to perform the duties, of a professor. Such temptations are very injurious to the true cause of science; and it were to be wished, that no literary body, in any part of the world, were possessed of such powers and privileges. When Bergman was rector, the university was divided into two great parties, the one consisting of the theological and law faculties, and the other of the scientific professors. Bergman's object was to preserve peace and agreement between these two parties, and to convince them that it was the interest of all to unite for the good of the university and the promotion of letters. The period of his magistracy is remarkable in the annals of the university for the small number of deliberations, and the little business recorded in the registers; and for the good sense and good behaviour of the students. The students in Upsala are numerous, and most of them are young men. They had been accustomed frequently to brave or elude the severity of the regulations; but during Bergman's rectorship they were restrained effectually by their respect for his genius, and their admiration of his character and conduct.
When the reputation of Bergman was at its height, in the year 1776, Frederick the Great of Prussia formed the wish to attach him to the Academy of Sciences of Berlin, and made him offers of such a nature that our professor hesitated for a short time as to whether he ought not to accept them. His health had been injured by the assiduity with which he had devoted himself to the double duty of teaching and experimenting. He might look for an alleviation of his ailments, if not a complete recovery, in the milder climate of Prussia, and he would be able to devote himself entirely to his academical duties; but other considerations prevented him from acceding to this proposal, tempting as it was. The King of Sweden had been his benefactor, and it was intimated to him that his leaving the kingdom would afflict that monarch. This information induced him, without further hesitation, to refuse the proposals of the King of Prussia. He requested of the king, his master, not to make him lose the merit of his sacrifice by augmenting his income; but to this demand the King of Sweden very properly refused to accede.
In the year 1771, Professor Bergman married a widow lady, Margaretha Catharina Trast, daughter of a clergyman in the neighbourhood of Upsala. By her he had two sons; but both of them died when infants. This lady survived her husband. The King of Sweden settled on her an annuity of 200 rix dollars, on condition that she gave up the library and apparatus of her late husband to the Royal Society of Upsala.
Bergman's health had been always delicate; indeed he seems never to have completely recovered the effects of his first year's too intense study at Upsala. He struggled on, however, with his ailments; and, by way of relaxation, was accustomed sometimes, in summer, to repair to the waters of Medevi—a celebrated mineral spring in Sweden, situated near the banks of the great inland lake, Wetter. One of these visits seems to have restored him to health for the time. But his malady returned in 1784 with redoubled violence. He was afflicted with hemorrhoids, and his daily loss of blood amounted to about six ounces. This constant drain soon exhausted him, and on the 8th of July, 1784, he died at the baths of Medevi, to which he had repaired in hopes of again benefiting by these waters.
The different tracts which he published, as they have been enumerated by Hjelm, who gave an interesting account of Bergman to the Stockholm Academy in the year 1785, amount to 106. They have been all collected into six octavo volumes entitled "Opuscula Torberni Bergman Physica et Chemica"—with the exception of his notes on Scheffer, his Sciagraphia, and his chapter on Physical Geography, which was translated into French, and published in the Journal des Mines (vol. iii. No. 15, p. 55). His Sciagraphia, which is an attempt to arrange minerals according to their composition, was translated into English by Dr. Withering. His notes on Scheffer were interspersed in an edition of the "Chemiske Föreläsningar" of that chemist, published in 1774, which he seems to have employed as a text-book in his lectures: or, at all events, the work was published for the use of the students of chemistry at Upsala. There was a new edition of it published, after Bergman's death, in the year 1796, to which are appended Bergman's Tables of Affinities.
The most important of Bergman's chemical papers were collected by himself, and constitute the three first volumes of his Opuscula. The three last volumes of that work were published after his death. The fourth volume was published at Leipsic, in 1787, by Hebenstreit, and contains the rest of his chemical papers. The fifth volume was given to the world in 1788, by the same editor. It contains three chemical papers, and the rest of it is made up with papers on natural history, electricity, and other branches of physics, which Bergman had published in the earlier part of his life. The same indefatigable editor published the sixth volume in 1790. It contains three astronomical papers, two chemical, and a long paper on the means of preventing any injurious effects from lightning. This was an oration, delivered before the Royal Academy of Sciences of Stockholm, in 1764, probably at the time of his admission into the academy.
It would serve little purpose in the present state of chemical knowledge, to give a minute analysis of Bergman's papers. To judge of their value, it would be necessary to compare them, not with our present chemical knowledge, but with the state of the science when his papers were published. A very short general view of his labours will be sufficient to convey an idea of the benefits which the science derived from them.
1. His first paper, entitled "On the Aerial Acid," that is, carbonic acid, was published in 1774. In it he gives the properties of this substance in considerable detail, shows that it possesses acid qualities, and that it is capable of combining with the bases, and forming salts. What is very extraordinary, in giving an account of carbonate of lime and carbonate of magnesia, he never mentions the name of Dr. Black; though it is very unlikely that a controversy, which had for years occupied the attention of chemists, should have been unknown to him. Mr. Cavendish's name never once appears in the whole paper; though that philosopher had preceded him by seven or eight years. He informs us, that he had made known his opinions respecting the nature of this substance, to various foreign correspondents, among others to Dr. Priestley, as early as the year 1770, and that Dr. Priestley had mentioned his views on the subject, in a paper inserted in the Philosophical Transactions for 1772. Bergman found the specific gravity of carbonic acid gas rather higher than 1·5, that of air being 1. His result is not far from the truth. He obtained his gas, by mixing calcareous spar with dilute sulphuric acid. He shows that this gas has a sour taste, that it reddens the infusion of litmus, and that it combines with bases. He gives figures of the apparatus which he used. This apparatus demands attention. Though far inferior to the contrivances of Priestley, it answered pretty well, enabling him to collect the gas, and examine its properties.
It is unnecessary to enter into any further details respecting this paper. Whoever will take the trouble to compare it with Cavendish's paper on the same subject, will find that he had been anticipated by that philosopher in a great many of his most important facts. Under these circumstances, I consider as singular his not taking any notice of Cavendish's previous labours.
2. His next paper, "On the Analyses of Mineral Waters," was first published in 1778, being the subject of a thesis, supported by J. P. Scharenberg. This dissertation, which is of great length, is entitled to much praise. He lays therein the foundation of the mode of analyzing waters, such as is followed at present. He points out the use of different reagents, for detecting the presence of the various constituents in mineral water, and then shows how the quantity of each is to be determined. It would be doing great injustice to Bergman, to compare his analyses with those of any modern experimenter. At that time, the science was not in possession of any accurate analyses of the neutral salts, which exist in mineral waters. Bergman undertook these necessary analyses, without which, the determination of the saline constituents of mineral waters was out of the question. His determinations were not indeed accurate, but they were so much better than those that preceded them, and Bergman's character as an experimenter stood so high, that they were long referred to as a standard by chemists. The first attempt to correct them was by Kirwan. But Bergman's superior reputation as a chemist enabled his results still to keep their ground, till his character for accuracy was finally destroyed by the very accurate experiments which the discovery of the atomic theory rendered it necessary to make. These, when once they became generally known, were of course preferred, and Bergman's analyses were laid aside.
It is a curious and humiliating fact, as it shows how much chemical reputation depends upon situation, or accidental circumstances, that Wenzel had, in 1766, in his book on affinity, published much more accurate analyses of all these salts, than Bergman's—analyses indeed which were almost perfectly correct, and which have scarcely been surpassed, by the most careful ones of the present day. Yet these admirable experiments scarcely drew the attention of chemists; while the very inferior ones of Bergman were held up as models of perfection.
3. Bergman, not satisfied with pointing out the mode of analyzing mineral waters, attempted to imitate them artificially by chemical processes, and published two essays on the subject; in the first he showed the processes by which cold mineral waters might be imitated, and in the other, the mode of imitating hot mineral waters. The attempt was valuable, and served to extend greatly the chemical knowledge of mineral waters, and of the salts which they contain; but it was made at too early a period of the analytical art, to approach perfection. A similar remark applies to his analysis of sea-water. The water examined was brought by Sparmann from a depth of eighty fathoms, near the latitude of the Canaries: Bergman found in it only common salt, muriate of magnesia, and sulphate of lime. His not having discovered the presence of sulphate of magnesia is a sufficient proof of the imperfection of his analytical methods; the other constituents exist in such small quantity in sea-water that they might easily have been overlooked, but the quantity of sulphate of magnesia in sea-water is considerable.
4. I shall pass over the paper on oxalic acid, which constituted the subject of a thesis, supported in 1776, by John Afzelius Arfvedson. It is now known that oxalic acid was discovered by Scheele, not by Bergman. It is impossible to say how many of the numerous facts stated in this thesis were ascertained by Scheele, and how many by Afzelius. For, as Afzelius was already a magister docens in chemistry, there can be little doubt that he would himself ascertain the facts which were to constitute the foundation of his thesis. It is indeed now known that Bergman himself intrusted all the details of his experiments to his pupils. He was the contriver, while his pupils executed his plans. That Scheele has nowhere laid claim to a discovery of so much importance as that of oxalic acid, and that he allowed Bergman peaceably to bear away the whole credit, constitutes one of the most remarkable facts in the history of chemistry. Moreover, while it reflects so much credit on Scheele for modesty and forbearance, it seems to bear a little hard upon the character of Bergman. When he published the essay in the first volume of his Opuscula, in 1779, why did he not in a note inform the world that Scheele was the true discoverer of this acid? Why did he allow the discovery to be universally assigned to him, without ever mentioning the true state of the case? All this appeared so contrary to the character of Bergman, that I was disposed to doubt the truth of the statement, that Scheele was the discoverer of oxalic acid. When I was at Fahlun, in the year 1812, I took an opportunity of putting the question to Assessor Gahn, who had been the intimate friend of Scheele, and the pupil, and afterwards the friend of Bergman. He assured me that Scheele really was the discoverer of oxalic acid, and ascribed the omission of Bergman to inadvertence. Assessor Gahn showed me a volume of Scheele's letters to him, which he had bound up: they contained the history of all his chemical labours. I have little doubt that an account of oxalic acid would be found in these letters. If the son of Assessor Gahn, in whose possession these letters must now be, would take the trouble to inspect the volume in question, and to publish any notices respecting this acid which they may contain, he would confer an important favour on every person interested in the history of chemistry.
5. The dissertation on the manufacture of alum has been mentioned before. Bergman shows himself well acquainted with the processes followed, at least in Sweden, for making alum. He had no notion of the true constitution of alum; nor was that to be expected, as the discovery was thereby years later in being made. He thought that the reason why alum leys did not crystallize well was, that they contained an excess of acid, and that the addition of potash gave them the property of crystallizing readily, merely by saturating that excess of acid. Alum is a double salt, composed of three integrant particles of sulphate of alumina, and one integrant particle of sulphate of potash, or sulphate of ammonia. In some cases, the alum ore contains all the requisite ingredients. This is the case with the ore at Tolfa, in the neighbourhood of Rome. It seems, also, to be the case with respect to some of the alum ores in Sweden; particularly at Hœnsœter on Kinnekulle, in West Gothland, which I visited in 1812. If any confidence can be put in the statements of the manager of those works, no alkaline salt whatever is added; at least, I understood him to say so when I put the question.
6. In his dissertation on tartar-emetic, he gives an interesting historical account of this salt and its uses. His notions respecting the antimonial preparations best fitted to form it, are not accurate: nor, indeed, could they be expected to be so, till the nature and properties of the different oxides of antimony were accurately known. Antimony forms three oxides: now it is the protoxide alone that is useful in medicine, and that enters into the composition of tartar-emetic; the other two oxides are inert, or nearly so. Bergman was aware that tartar-emetic is a double salt, and that its constituents are tartaric acid, potash, and oxide of antimony; but it was not possible, in 1773, when his dissertation was published, to have determined the true constituents of this salt by analysis.
7. Bergman's paper on magnesia was also a thesis defended in 1775, by Charles Norell, of West Gothland, who in all probability made the experiments described in the essay. In the introduction we have a history of the discovery of magnesia, and he mentions Dr. Black as the person who first accurately made out its peculiar chemical characters, and demonstrated that it differs from lime. This essay contains a pretty full and accurate account of the salts of magnesia, considering the state of chemistry at the time when it was published. There is no attempt to analyze any of the magnesian salts; but, in his treatise on the analysis of mineral waters, he had stated the quantity of magnesia contained in one hundred parts of several of them.
8. His paper on the shapes of crystals, published in 1773, contains the germ of the whole theory of crystallization afterwards developed by M. Hauy. He shows how, from a very simple primary form of a mineral, other shapes may proceed, which seem to have no connexion with, or resemblance to the primary form. His view of the subject, so far as it goes, is the very same afterwards adopted by Hauy: and, what is very curious, Hauy and Bergman formed their theory from the very same crystalline shape of calcareous spar—from which, by mechanical divisions, the same rhombic nucleus was extracted by both. Nothing prevented Bergman from anticipating Hauy but a sufficient quantity of crystals to apply his theory to.[2]
9. In his paper on silica he gives us a history of the progress of chemical knowledge respecting this substance. Its nature was first accurately pointed out by Pott; though Glauber, and before him Van Helmont, were acquainted with the liquor silicus, or the combination of silica and potash, which is soluble in water. Bergman gives a detailed account of its properties; but he does not suspect it to possess acid properties. This great discovery, which has thrown a new light upon mineral bodies, and shown them all to be chemical combinations, was reserved for Mr. Smithson.
10. Bergman's experiments on the precious stones constitute the first rudiments of the method of analyzing stony bodies. His processes are very imperfect, and his apparatus but ill adapted to the purpose. We need not be surprised, therefore, that the results of his analyses are extremely wide of the truth. Yet, if we study his processes, we shall find in them the rudiments of the very methods which we follow at present. The superiority of the modern analyses over those of Bergman must in a great measure be ascribed to the platinum vessels which we now employ, and to the superior purity of the substances which we use as reagents in our analyses. The methods, too, are simplified and perfected. But we must not forget that this paper of Bergman's, imperfect as it is, constitutes the commencement of the art, and that fully as much genius and invention may be requisite to contrive the first rude processes, how imperfect soever they may be, as are required to bring these processes when once invented to a state of comparative perfection. The great step in analyzing minerals is to render them soluble in acids. Bergman first thought of the method for accomplishing this which is still followed, namely, fusing them or heating them to redness with an alkali or alkaline carbonate.
11. The paper on fulminating gold goes a great way to explain the nature of that curious compound. He describes the properties of this substance, and the effects of alkaline and acid bodies on it. He shows that it cannot be formed without ammonia, and infers from his experiments that it is a compound of oxide of gold and ammonia. He explains the fulmination by the elastic fluid suddenly generated by the decomposition of the ammonia.
12. The papers on platinum, carbonate of iron, nickel, arsenic, and zinc, do not require many remarks. They add considerably to the knowledge which chemists at that time possessed of these bodies; though the modes of analysis are not such as would be approved of by a modern chemist; nor were the results obtained possessed of much precision.
13. The Essay on the Analysis of Metallic Ores by the wet way, or by solution, constitutes the first attempt to establish a regular method of analyzing metallic ores. The processes are all imperfect, as might be expected from the then existing state of analytical chemistry, and the imperfect knowledge possessed, of the different metallic ores. But this essay constituted a first beginning, for which the author is entitled to great praise. The subject was taken up by Klaproth, and speedily brought to a great degree of improvement by the labours of modern chemists.
14. The experiments on the way in which minerals behave before the blowpipe, which Bergman published, were made at Bergman's request by Assessor Gahn, of Fahlun, who was then his pupil. They constitute the first results obtained by that very ingenious and amiable man. He afterwards continued the investigation, and added many improvements, simplifying the reagents and the manner of using them. But he was too indolent a man to commit the results of his investigations to writing. Berzelius, however, had the good sense to see the importance of the facts which Gahn had ascertained. He committed them to writing, and published them for the use of mineralogists. They constitute the book entitled "Berzelius on the Blowpipe," which has been translated into English.
15. The object of the Essay on Metallic Precipitates is to determine the quantity of phlogiston which each metal contains, deduced from the quantity of one metal necessary to precipitate a given weight of another. The experiments are obviously made with little accuracy: indeed they are not susceptible of very great precision. Lavoisier afterwards made use of the same method to determine the quantity of oxygen in the different metallic oxides; but his results were not more successful than those of Bergman.
16. Bergman's paper on iron is one of the most important in his whole works, and contributed very materially to advance the knowledge of the cause of the difference between iron and steel. He employed his pupils to collect specimens of iron from the different Swedish forges, and gave them directions how to select the proper pieces. All these specimens, to the number of eighty-nine, he subjected to a chemical examination, by dissolving them in dilute sulphuric acid. He measured the volume of hydrogen gas, which he obtained by dissolving a given weight of each, and noted the quantity and the nature of the undissolved residue. The general result of the whole investigation was that pure malleable iron yielded most hydrogen gas; steel less, and cast-iron least of all. Pure malleable iron left the smallest quantity of insoluble matter, steel a greater quantity, and cast-iron the greatest of all. From these experiments he drew conclusions with respect to the difference between iron, steel, and cast-iron. Nothing more was necessary than to apply the antiphlogistic theory to these experiments, (as was done soon after by the French chemists,) in order to draw important conclusions respecting the nature of these bodies. Iron is a simple body; steel is a compound of iron and carbon; and cast-iron of iron and a still greater proportion of carbon. The defective part of the experiments of Bergman in this important paper is his method of determining the quantity of manganese in iron. In some specimens he makes the manganese amount to considerably more than a third part of the weight of the whole. Now we know that a mixture of two parts iron and one part manganese is brittle and useless. We are sure, therefore, that no malleable iron whatever can contain any such proportion of manganese. The fact is, that Bergman's mode of separating manganese from iron was defective. What he considered as manganese was chiefly, and might be in many cases altogether, oxide of iron. Many years elapsed before a good process for separating iron from manganese was discovered.
17. Bergman's experiments to ascertain the cause of the brittleness of cold-short iron need not occupy much of our attention. He extracted from it a white powder, by dissolving the cold-short iron in dilute sulphuric acid. This white powder he succeeded in reducing to the state of a white brittle metal, by fusing it with a flux and charcoal. Klaproth soon after ascertained that this metal was a phosphuret of iron, and that the white powder was a phosphate of iron: and Scheele, with his usual sagacity, hit on a method of analyzing this phosphate, and thus demonstrating its nature. Thus Bergman's experiments led to the knowledge of the fact that cold-short iron owes its brittleness to a quantity of phosphorus which it contains. It ought to be mentioned that Meyer, of Stettin, ascertained the same fact, and made it known to chemists at about the same time with Bergman.
18. The dissertation on the products of volcanoes, first published in 1777, is one of the most striking examples of the sagacity of Bergman which we possess. He takes a view of all the substances certainly known to have been thrown out of volcanoes, attempts to subject them to a chemical analysis, and compares them with the basalt, and greenstone or trap-rocks, the origin of which constituted at that time a keen matter of dispute among geologists. He shows the identity between lavas and basalt and greenstone, and therefore infers the identity of formation. This is obviously the true mode of proceeding, and, had it been adopted at an earlier period, many of those disputes respecting the nature of trap-rocks, which occupied geologists for so long a period, would never have been agitated; or, at least, would have been speedily decided. The whole dissertation is filled with valuable matter, still well entitled to the attention of geologists. His observations on zeolites, which he considered as unconnected with volcanic products, were very natural at the time when he wrote: though the subsequent experiments of Sir James Hall, and Mr. Gregory Watt, and, above all, an accurate attention to the scoriæ from different smelting-houses, have thrown a new light on the subject, and have shown the way in which zeolitic crystals might easily have been formed in melted lava, provided circumstances were favourable. In fact, we find abundant cavities in real lava from Vesuvius, filled with zeolitic crystals.
19. The last of the labours of Bergman which I shall notice here is his Essay on Elective Attractions, which was originally published in 1775, but was much augmented and improved in the third volume of his Opuscula, published in 1783. An English translation of this last edition of the Essay was made by Dr. Beddoes, and was long familiar to the British chemical world. The object of this essay was to elucidate and explain the nature of chemical affinity, and to account for all the apparent anomalies that had been observed. He laid it down as a first principle, that all bodies capable of combining chemically with each other, have an attraction for each other, and that this attraction is a definite and fixed force which may be represented by a number. Now the bodies which have the property of uniting together are chiefly the acids and the alkalies, or bases. Every acid has an attraction for each of the alkalies or bases; but the force of this attraction differs in each. Some bases have a strong attraction for acids, and others a weak; but the attractive force of each may be expressed by numbers.
Now, suppose that an acid a is united with a base m with a certain force, if we mix the compound a m with a certain quantity of the base n, which has a stronger attraction for a than m has, the consequence will be, that a will leave m and unite with n;—n having a stronger attraction for a than m has, will disengage it and take its place. In consequence of this property, which Bergman considered as the foundation of the whole of the science, the strength of affinity of one body for another is determined by these decompositions and combinations. If n has a stronger affinity for a than m has, then if we mix together a, m, and n in the requisite proportions, a and n will unite together, leaving m uncombined: or if we mix n with the compound a m, m will be disengaged. Tables, therefore, may be drawn up, exhibiting the strength of these affinities. At the top of a column is put the name of an acid or a base, and below it are put the names of all the bases or acids in the order of their affinity. The following little table will exhibit a specimen of these columns:
- Sulphuric Acid.
- Barytes
- Strontian
- Potash
- Soda
- Lime
- Magnesia.
Here sulphuric acid is the substance placed at the head of the column, and under it are the names of the bases capable of uniting with it in the order of their affinity. Barytes, which is highest up, has the strongest affinity, and magnesia, which is lowest down, has the weakest affinity. If sulphuric acid and magnesia were combined together, all the bases whose names occur in the table above magnesia would be able to separate the sulphuric acid from it. Potash would be disengaged from sulphuric acid by barytes and strontian, but not by soda, lime, and magnesia.
Such tables then exhibited to the eye the strength of affinity of all the different bodies that are capable of uniting with one and the same substance, and the order in which decompositions are effected. Bergman drew up tables of affinity according to these views in fifty-nine columns. Each column contained the name of a particular substance, and under it was arranged all the bodies capable of uniting with it, each in the order of its affinity. Now bodies may be made to unite, either by mixing them together, and then exposing them to heat, or by dissolving them in water and mixing the respective solutions together. The first of these ways is usually called the dry way, the second the moist way. The order of decompositions often varies with the mode employed. On this account, Bergman divided each of his fifty-nine columns into two. In the first, he exhibited the order of decompositions in the moist way, in the second in the dry. He explained also the cases of double decomposition, by means of these unvarying forces acting together or opposing each other—and gave sixty-four cases of such double decompositions.
These views of Bergman's were immediately acceded to by the chemical world, and continued to regulate their processes till Berthollet published his Chemical Statics in 1802. He there called in question the whole doctrine of Bergman, and endeavoured to establish one of the very opposite kind. I shall have occasion to return to the subject when I come to give an account of the services which Berthollet conferred upon chemistry.
I have already observed, that we are under obligations to Bergman, not merely for the improvements which he himself introduced into chemistry, but for the pupils whom he educated as chemists, and the discoveries which were made by those persons, whose exertions he stimulated and encouraged. Among those individuals, whose chemical discoveries were chiefly made known to the world by his means, was Scheele, certainly one of the most extraordinary men, and most sagacious and industrious chemists that ever existed.
Charles William Scheele was born on the 19th of December, 1742, at Stralsund, the capital of Swedish Pomerania, where his father was a tradesman. He received the first part of his education at a private academy in Stralsund, and was afterwards removed to a public school. At a very early period he expressed a strong desire to study pharmacy, and obtained his father's consent to make choice of this profession. He was accordingly bound an apprentice for six years to Mr. Bouch, an apothecary in Gotheborg, and after his time was out, he remained with him still, two years longer.
It was here that he laid the groundwork of all his future celebrity, as we are informed by Mr. Grunberg, who was his fellow-apprentice, and afterwards settled as an apothecary in Stralsund. He was at that time very reserved and serious, but uncommonly diligent. He attended minutely to all the processes, reflected upon them while alone, and studied the writings of Neumann, Lemery, Kunkel, and Stahl, with indefatigable industry. He likewise exercised himself a good deal in drawing and painting, and acquired some proficiency in these accomplishments without a master. Kunkel's Laboratorium was his favourite book, and he was in the habit of repeating experiments out of it secretly during the night-time. On one occasion, as he was employed in making pyrophorus, his fellow-apprentice was malicious enough to put a quantity of fulminating powder into the mixture. The consequence was a violent explosion, which, as it took place in the night, threw the whole family into confusion, and brought a very severe rebuke upon our young chemist. But this did not put a stop to his industry, which he pursued so constantly and judiciously, that, by the time his apprenticeship was ended, there were very few chemists indeed who excelled him in knowledge and practical skill. His fellow-apprentice, Mr. Grunberg, wrote to him in 1774, requesting to know by what means he had become such a proficient in chemistry, and received the following answer: "I look upon you, my dear friend, as my first instructor, and as the author of all I know on the subject, in consequence of your advising me to read Neumann's Chemistry. The perusal of this book first gave me a taste for experimenting, myself; and I very well remember, that upon mixing some oil of cloves and smoking spirit of nitre together, they took fire. However, I kept this matter secret. I have also before my eyes the unfortunate experiment which I made with pyrophorus. Such accidents only served to increase my passion for making experiments."
In 1765 Scheele went to Malmo, to the house of an apothecary, called Mr. Kalstrom. After spending two years in that place, he went to Stockholm, to superintend the apothecary's shop of Mr. Scharenberg. In 1773 he exchanged this situation for another at Upsala, in the house of Mr. Loock. It was here that he accidentally formed an acquaintance with Assessor Gahn, of Fahlun, who was at that time a student at Upsala, and a zealous chemist. Mr. Gahn happening to be one day in the shop of Mr. Loock, that gentleman mentioned to him a circumstance which had lately occurred to him, and of which he was anxious to obtain an explanation. If a quantity of saltpetre be put into a crucible and raised to such a temperature as shall not merely melt it, but occasion an agitation in it like boiling, and if, after a certain time, the crucible be taken out of the fire and allowed to cool, the saltpetre still continues neutral; but its properties are altered: for, if distilled vinegar be poured upon it, red fumes are given out, while vinegar produces no effect upon the saltpetre before it has been thus heated. Mr. Loock wished from Gahn an explanation of the cause of this phenomenon: Gahn was unable to explain it; but promised to put the question to Professor Bergman. He did so accordingly, but Bergman was as unable to find an explanation as himself. On returning a few days after to Mr. Loock's shop, Gahn was informed that there was a young man in the shop who had given an explanation of the phenomenon. This young man was Scheele, who had informed Mr. Loock that there were two species of acids confounded under the name of spirit of nitre; what we at present call nitric and hyponitrous acids. Nitric acid has a stronger affinity for potash than vinegar has; but hyponitrous acid has a weaker. The heat of the fire changes the nitric acid of the saltpetre to hyponitrous: hence the phenomenon.
Gahn was delighted with the information, and immediately formed an acquaintance with Scheele, which soon ripened into friendship. When he informed Bergman of Scheele's explanation, the professor was equally delighted, and expressed an eager desire to be made acquainted with Scheele; but when Gahn mentioned the circumstance to Scheele, and offered to introduce him to Bergman, our young chemist rejected the proposal with strong feelings of dislike.
It seems, that while Scheele was in Stockholm, he had made experiments on cream of tartar, and had succeeded in separating from it tartaric acid, in a state of purity. He had also determined a number of the properties of tartaric acid, and examined several of the tartrates. He drew up an account of these results, and sent it to Bergman. Bergman, seeing a paper subscribed by the name of a person who was unknown to him, laid it aside without looking at it, and forgot it altogether. Scheele was very much provoked at this contemptuous and unmerited treatment. He drew up another account of his experiments and gave it to Retzius, who sent it to the Stockholm Academy of Sciences (with some additions of his own), in whose Memoirs it was published in the year 1770.[3] It cost Assessor Gahn considerable trouble to satisfy Scheele that Bergman's conduct was merely the result of inadvertence, and that he had no intention whatever of treating him either with contempt or neglect. After much entreaty, he prevailed upon Scheele to allow him to introduce him to the professor of chemistry. The introduction took place accordingly, and ever after Bergman and Scheele continued steady friends—Bergman facilitating the researches of Scheele by every means in his power.
So high did the character of Scheele speedily rise in Upsala, that when the Duke of Sudermania visited the university soon after, in company with Prince Henry of Prussia, Scheele was appointed by the university to exhibit some chemical processes before him. He fulfilled his charge, and performed in different furnaces several curious and striking experiments. Prince Henry asked him various questions, and expressed satisfaction at the answers given. He was particularly pleased when informed that he was a native of Stralsund. These two princes afterwards stated to the professors that they would take it as a favour if Scheele could have free access to the laboratory of the university whenever he wished to make experiments.
In the year 1775, on the death of Mr. Popler, apothecary at Köping (a small place on the north side of the lake Mæler), he was appointed by the Medical College provisor of the apothecary's shop. In Sweden all the apothecaries are under the control of the Medical College, and no one can open a shop without undergoing an examination and receiving licence from that learned body. In the course of the examinations which he was obliged to undergo, Scheele gave great proofs of his abilities, and obtained the appointment. In 1777 the widow sold him the shop and business, according to a written agreement made between them; but they still continued housekeeping at their joint expense. He had already distinguished himself by his discovery of fluoric acid, and by his admirable paper on manganese. It is said, too, that it was he who made the experiments on carbonic acid gas, which constitute the substance of Bergman's paper on the subject, and which confirmed and established Bergman's idea that it was an acid. At Köping he continued his researches with unremitting perseverance, and made more discoveries than all the chemists of his time united together. It was here that he made the experiments on air and fire, which constitute the materials of his celebrated work on these subjects. The theory which he formed was indeed erroneous; but the numerous discoveries which the book contains must always excite the admiration of every chemist. His discovery of oxygen gas had been anticipated by Priestley; but his analysis of atmospheric air was new and satisfactory—was peculiarly his own. The processes by means of which he procured oxygen gas were also new, simple, and easy, and are still followed by chemists in general. During his residence at Köping he published a great number of chemical papers, and every one of them contained a discovery. The whole of his time was devoted to chemical investigations. Every action of his life had a tendency to forward the advancement of his favourite science; all his thoughts were turned to the same object; all his letters were devoted to chemical observations and chemical discussions. Crell's Annals was at that time the chief periodical work on chemistry in Germany. He got the numbers regularly as they were published, and was one of Crell's most constant and most valuable correspondents. Every one of his letters published in that work either contains some new chemical fact, or exposes the errors and mistakes of some one or other of Crell's numerous correspondents.
Scheele's outward appearance was by no means prepossessing. He seldom joined in the usual conversations and amusements of society, having neither leisure nor inclination for them. What little time he had to spare from the hurry of his profession was always employed in making experiments. It was only when he received visits from his friends, with whom he could converse on his favourite science, that he indulged himself in a little relaxation. For such intimate friends he had a sincere affection. This regard was extended to all the zealous cultivators of chemistry in every part of the world, whether personally known to him or not. He kept up a correspondence with several; though this correspondence was much limited by his ignorance of all languages except German; for at least he could not write fluently in any other language. His chemical papers were always written in German, and translated into Swedish, before they were inserted in the Memoirs of the Stockholm Academy, where most of them appeared.
He was kind and affable to all. Before he adopted an opinion in science, he reflected maturely on it; but, after he had once embraced it, his opinions were not easily shaken. However, he did not hesitate to give up an opinion as soon as it had been proved to be erroneous. Thus, he entirely renounced the notion which he once entertained that silica is a compound of water and fluoric acid; because it was demonstrated, by Meyer and others, that this silica was derived from the glass vessels in which the fluoric acid was prepared; that these glass vessels were speedily corroded into holes; and that, if fluoric acid was prepared in metallic vessels, and not allowed to come in contact with glass or any substance containing silica, it might be mixed with water without any deposition of silica whatever.
It appears also by a letter of his, published in Crell's Annals, that he was satisfied of the accuracy of Mr. Cavendish's experiments, showing that water was a compound of oxygen and hydrogen gases, and of Lavoisier's repetition of them. He attempted to reconcile this fact with his own notion, that heat is a compound of oxygen and hydrogen. But his arguments on that subject, though ingenious, are not satisfactory; and there is little doubt that if he had lived somewhat longer, and had been able to repeat his own experiments, and compare them with those of Cavendish and Lavoisier, he would have given up his own theory and adopted that of Lavoisier, or, at any rate, the explanation of Cavendish, which, being more conformable to his own preconceived notions, might have been embraced by him in preference.
It is said by Dr. Crell that Scheele was invited over to England, with an offer of an easy and advantageous situation; but that his love of quiet and retirement, and his partiality for Sweden, where he had spent the greatest part of his life, threw difficulties in the way of these overtures, and that a change in the English ministry put a stop to them for the time. The invitation, Crell says, was renewed in 1786, with the offer of a salary of 300l. a-year; but Scheele's death put a final stop to it. I have very great doubts about the truth of this statement; and, many years ago, during the lifetime of Sir Joseph Banks, Mr. Cavendish, and Mr. Kirwan, I made inquiry about the circumstance; but none of the chemists in Great Britain, who were at that time numerous and highly respectable, had ever heard of any such negotiation. I am utterly at a loss to conceive what one individual in any of the ministries of George III. was either acquainted with the science of chemistry, or at all interested in its progress. They were all so intent upon accomplishing their own objects, or those of their sovereign, that they had neither time nor inclination to think of science, and certainly no money to devote to any of its votaries. What minister in Great Britain ever attempted to cherish the sciences, or to reward those who cultivate them with success? If we except Mr. Montague, who procured the place of master of the Mint for Sir Isaac Newton, I know of no one. While in every other nation in Europe science is directly promoted, and considerable sums are appropriated for its cultivation, and for the support of a certain number of individuals who have shown themselves capable of extending its boundaries, not a single farthing has been devoted to any such purpose in Great Britain. Science has been left entirely to itself; and whatever has been done by way of promoting it has been performed by the unaided exertions of private individuals. George III. himself was a patron of literature and an encourager of botany. He might have been disposed to reward the unrivalled eminence which Scheele had attained; but this he could only have done by bestowing on him a pension out of his privy purse. No situation which Scheele could fill was at his disposal. The universities and the church were both shut against a Lutheran; and no pharmaceutical places exist in this country to which Scheele could have been appointed. If any such project ever existed, it must have been an idea which struck some man of science that such a proposal to a man of Scheele's eminence would redound to the credit of the country. But that such a project should have been broached by a British ministry, or by any man of great political influence, is an opinion that no person would adopt who has paid any attention to the history of Great Britain since the Revolution to the present time.
Scheele fell at last a sacrifice to his ardent love for his science. He was unable to abstain from experimenting, and many of his experiments were unavoidably made in his shop, where he was exposed during winter, in the ungenial climate of Sweden, to cold draughts of air. He caught rheumatism in consequence, and the disease was aggravated by his ardour and perseverance in his pursuits. When he purchased the apothecary's shop in which his business was carried on, he had formed the resolution of marrying the widow of his predecessor, and he had only delayed it from the honourable principle of acquiring, in the first place, sufficient property to render such an alliance desirable on her part. At length, in the month of March, 1786, he declared his intention of marrying her; but his disease at this time increased very fast, and his hopes of recovery daily diminished. He was sensible of this; but nevertheless he performed his promise, and married her on the 19th of May, at a time when he lay on his deathbed. On the 21st, he left her by his will the disposal of the whole of his property; and, the same day on which he so tenderly provided for her, he died.
I shall now endeavour to give the reader an idea of the principal chemical discoveries for which we are indebted to Scheele: his papers, with the exception of his book on air and fire, which was published separately by Bergman, are all to be found either in the Memoirs of the Stockholm Academy of Science, or in Crell's Journal; they were collected, and a Latin translation of them, made by Godfrey Henry Schaefer, published at Leipsic, in 1788, by Henstreit, the editor of the three last volumes of Bergman's Opuscula. A French translation of them was made in consequence of the exertions of M. Morveau; and an English translation of them, in 1786, by means of Dr. Beddoes, when he was a student in Edinburgh. There are also several German translations, but I have never had an opportunity of seeing them.
1. Scheele's first paper was published by Retzius, in 1770; it gives a method of obtaining pure tartaric acid: the process was to decompose cream of tartar by means of chalk. One half of the tartaric acid unites to the lime, and falls down in the state of a white insoluble powder, being tartrate of lime. The cream of tartar, thus deprived of half its acid, is converted into the neutral salt formerly distinguished by the name of soluble tartar, from its great solubility in water: it dissolves, and may be obtained in crystals, by the usual method of crystallizing salts. The tartrate of lime is washed with water, and then mixed with a quantity of dilute sulphuric acid, just capable of saturating the lime contained in the tartrate of lime; the mixture is digested for some time; the sulphuric acid displaces the tartaric acid, and combines with the lime; and, as the sulphate of lime is but very little soluble in water, the greatest part of it precipitates, and the clear liquor is drawn off: it consists of tartaric acid, held in solution by water, but not quite free from sulphate of lime. By repeated concentrations, all the sulphate of lime falls down, and at last the tartaric acid itself is obtained in large crystals. This process is still followed by the manufacturers of this country; for tartaric acid is used to a very considerable extent by the calico-printers, in various processes; for example, it is applied, thickened with gum, to different parts of cloth dyed Turkey red; the cloth is then passed through water containing the requisite quantity of chloride of lime: the tartaric acid, uniting with the lime, sets the chlorine at liberty, which immediately destroys the red colour wherever the tartaric acid has been applied, but leaves all the other parts of the cloth unchanged.
2. The paper on fluoric acid appeared in the Memoirs of the Stockholm Academy, for 1771, when Scheele was in Scharenberg's apothecary's shop in Stockholm, where, doubtless, the experiments were made. Three years before, Margraaf had attempted an analysis of fluor spar, but had discovered nothing. Scheele demonstrated that it is a compound of lime and a peculiar acid, to which he gave the name of fluoric acid. This acid he obtained in solution in water; it was separated from the fluor spar by sulphuric, muriatic, nitric, and phosphoric acids. When the fluoric acid came in contact with water, a white crust was formed, which proved, on examination, to be silica. Scheele at first thought that this silica was a compound of fluoric acid and water; but it was afterwards proved by Weigleb and by Meyer, that this notion is inaccurate, and that the silica was corroded from the retort into which the fluor spar and sulphuric acid were put. Bergman, who had adopted Scheele's theory of the nature of silica, was so satisfied by these experiments, that he gave it up, as Scheele himself did soon after.
Scheele did not obtain fluoric acid in a state of purity, put only fluosilicic acid; nor were chemists acquainted with the properties of fluoric acid till Gay-Lussac and Thenard published their Recherches Physico-chimiques, in 1811.
3. Scheele's experiments on manganese were undertaken at the request of Bergman, and occupied him three years; they were published in the Memoirs of the Stockholm Academy, for 1774, and constitute the most memorable and important of all his essays, since they contain the discovery of two new bodies, which have since acted so conspicuous a part, both in promoting the progress of the science, and in improving the manufactures of Europe. These two substances are chlorine and barytes, the first account of both of which occur in this paper.
The ore of manganese employed in these experiments was the black oxide, or deutoxide, of manganese, as it is now called. Scheele's method of proceeding was to try the effect of all the different reagents on it. It dissolved in sulphurous and nitrous acids, and the solution was colourless. Dilute sulphuric acid did not act upon it, nor nitric acid; but concentrated sulphuric acid dissolved it by the assistance of heat. The solution of sulphate of manganese in water was colourless and crystallized in very oblique rhomboidal prisms, having a bitter taste. Muriatic acid effervesced with it, when assisted by heat, and the elastic fluid that passed off had a yellowish colour, and the smell of aqua regia. He collected quantities of this elastic fluid (chlorine) in bladders, and determined some of its most remarkable properties: it destroyed colours, and tinged the bladder yellow, as nitric acid does. This elastic fluid, in Scheele's opinion, was muriatic acid deprived of phlogiston. By phlogiston Scheele meant, in this place, hydrogen gas. He considered muriatic acid as a compound of chlorine and hydrogen. Now this is the very theory that was established by Davy in consequence of his own experiments and those of Gay-Lussac and Thenard. Scheele's mode of collecting chlorine gas in a bladder, did not enable him to determine its characters with so much precision as was afterwards done. But his accuracy was so great, that every thing which he stated respecting it was correct so far as it went.
Most of the specimens of manganese ore which Scheele examined, contained more or less barytes, as has since been determined, in combination with the oxide. He separated this barytes, and determined its peculiar properties. It dissolved in nitric and muriatic acids, and formed salts capable of crystallizing, and permanent in the air. Neither potash, soda, nor lime, nor any base whatever, was capable of precipitating it from these acids. But the alkaline carbonates threw it down in the state of a white powder, which dissolved with effervescence in acids. Sulphuric acid and all the sulphates threw it down in the state of a white powder, which was insoluble in water and in acids. This sulphate cannot be decomposed by any acid or base whatever. The only practicable mode of proceeding is to convert the sulphuric acid into sulphur, by heating the salt with charcoal powder, along with a sufficient quantity of potash, to bring the whole into fusion. The fused mass, edulcorated, is soluble in nitric or muriatic acid, and thus may be freed from charcoal, and the barytes obtained in a state of purity. Scheele detected barytes, also, in the potash made from trees or other smaller vegetables; but at that time he was unacquainted with sulphate of barytes, which is so common in various parts of the earth, especially in lead-mines.
To point out all the new facts contained in this admirable essay, it would be necessary to transcribe the whole of it. He shows the remarkable analogy between manganese and metallic oxides. Bergman, in an appendix affixed to Scheele's paper, states his reasons for being satisfied that it is really a metallic oxide. Some years afterwards, Assessor Gahn succeeded in reducing it to the metallic state, and thus dissipating all remaining doubts on the subject.
4. In 1775 he gave a new method of obtaining benzoic acid from benzoin. His method was, to digest the benzoin with pounded chalk and water, till the whole of the acid had combined with lime, and dissolved in the water. It is requisite to take care to prevent the benzoin from running into clots. The liquid thus containing benzoate of lime in solution is filtered, and muriatic acid added in sufficient quantity to saturate the lime. The benzoic acid is separated in white flocks, which may be easily collected and washed. This method, though sufficiently easy, is not followed by practical chemists, at least in this country. The acid when procured by precipitation is not so beautiful as what is procured by sublimation; nor is the process so cheap or so rapid. For these reasons, Scheele's process has not come into general use.
5. During the same year, 1775, his essay on arsenic and its acid was also published in the Memoirs of the Stockholm Academy. In this essay he shows various processes, by means of which white arsenic may be converted into an acid, having a very sour taste, and very soluble in water. This is the acid to which the name of arsenic acid has been since given. Scheele describes the properties of this acid, and the salts which it forms, with the different bases. He examines, also, the action of white arsenic upon different bodies, and throws light upon the arsenical salt of Macquer.
6. The object of the little paper on silica, clay, and alum, published in the Memoirs of the Stockholm Academy, for 1776, is to prove that alumina and silica are two perfectly distinct bodies, possessed of different properties. This he does with his usual felicity of experiment. He shows, also, that alumina and lime are capable of combining together.
7. The same year, and in the same volume of the Stockholm Memoirs, he published his experiments on a urinary calculus. The calculus upon which his experiments were made, happened to be composed of uric acid. He determined the properties of this new acid, particularly the characteristic one of dissolving in nitric acid, and leaving a beautiful pink sediment when the solution is gently evaporated to dryness.
8. In 1778 appeared his experiments on molybdena. What is now called molybdena is a soft foliated mineral, having the metallic lustre, and composed of two atoms sulphur united to one atom of metallic molybdenum. It was known before, from the experiments of Quest, that this substance contains sulphur. Scheele extracted from it a white powder, which he showed to possess acid properties, though it was insoluble in water. He examined the characters of this acid, called molybdic acid, and the nature of the salts which it is capable of forming by uniting with bases.
9. In the year 1777 was published the Experiments of Scheele on Air and Fire, with an introduction, by way of preface, from Bergman, who seems to have superintended the publication. This work is undoubtedly the most extraordinary production that Scheele has left us; and is really wonderful, if we consider the circumstances under which it was produced. Scheele ascertained that common air is a mixture of two distinct elastic fluids, one of which alone is capable of supporting combustion, and which, therefore, he calls empyreal air; the other, being neither capable of maintaining combustion, nor of being breathed, he called foul air. These are the oxygen and azote of modern chemists. Oxygen he showed to be heavier than common air; bodies burnt in it with much greater splendour than in common air. Azote he found lighter than common air; bodies would not burn in it at all. He showed that metallic calces, or metallic oxides, as they are now called, contain oxygen as a constituent, and that when they are reduced to the metallic state, oxygen gas is disengaged. In his experiments on fulminating gold he shows, that during the fulmination a quantity of azotic gas is disengaged; and he deduces from a great many curious facts, which are stated at length, that ammonia is a compound of azote and hydrogen. His apparatus was not nice enough to enable him to determine the proportions of the various ingredients of the bodies which he analyzed: accordingly that is seldom attempted; and when it is, as was the case with common air, the results are very unsatisfactory. He deduces from his experiments, that the volume of oxygen gas, in common air, is between a third and a fourth: we now know that it is exactly a fifth.
In this book, also, we have the first account of sulphuretted hydrogen gas, and of its properties. He gives it the name of stinking sulphureous air.
The observations and new views respecting heat and light in this work are so numerous, that I am obliged to omit them: nor do I think it necessary to advert to his theory, which, when his book was published, was exceedingly plausible, and undoubtedly constituted a great step towards the improvements which soon after followed. His own experiments, had he attended a little more closely to the weights, and the alterations of them, would have been sufficient to have overturned the whole doctrine of phlogiston. Upon the whole it may be said, with confidence, that there is no chemical book in existence which contains a greater number of new and important facts than this work of Scheele, at the time it was published. Yet most of his discoveries were made, also, by others. Priestley and Lavoisier, from the superiority of their situations, and their greater means of making their labours speedily known to the public, deprived him of much of that reputation to which, in common circumstances, he would have been entitled. Priestley has been blamed for the rapidity of his publications, and the crude manner in which he ushered his discoveries to the world. But had he kept them by him till he had brought them to a sufficient degree of maturity, it is obvious that he would have been anticipated in the most important of them by Scheele.
10. In the Memoirs of the Stockholm Academy, for 1779, there is a short but curious paper of Scheele, giving an account of some results which he had obtained. If a plate of iron be moistened by a solution of common salt, or of sulphate of soda, and left for some weeks in a moist cellar, an efflorescence of carbonate of soda covers the surface of the plate. The same decomposition of common salt and evolution of soda takes place when unslacked quicklime is moistened with a solution of common salt, and left in a similar situation. These experiments led afterwards to various methods of decomposing common salt, and obtaining from it carbonate of soda. The phenomena themselves are still wrapped up in considerable obscurity. Berthollet attempted an explanation afterwards in his Chemical Statics; but founded on principles not easily admissible.
11. During the same year, his experiments on plumbago were published. This substance had been long employed for making black-lead pencils; but nothing was known concerning its nature. Scheele, with his usual perseverance, tried the effect of all the different reagents, and showed that it consisted chiefly of carbon, but was mixed with a certain quantity of iron. It was concluded from these experiments, that plumbago is a carburet of iron. But the quantity of iron differs so enormously in different specimens, that this opinion cannot be admitted. Sometimes the iron amounts only to one-half per cent., and sometimes to thirty per cent. Plumbago, then, is carbon mixed with a variable proportion of iron, or carburet of iron.
12. In 1780 Scheele published his experiments on milk, and showed that sour milk contains a peculiar acid, to which the name of lactic acid has been given.
He found that when sugar of milk is dissolved in nitric acid, and the solution allowed to cool, small crystalline grains were deposited. These grains have an acid taste, and combine with bases: they have peculiar properties, and therefore constitute a particular acid, to which the name of saclactic was given. It is formed, also, when gum is dissolved in nitric acid; on this account it has been called, mucic acid.
13. In 1781 his experiments on a heavy mineral called by the Swedes tungsten, were published. This substance had been much noticed on account of its great weight; but nothing was known respecting its nature. Scheele, with his usual skill and perseverance, succeeded in proving that it was a compound of lime and a peculiar acid, to which the name of tungstic acid was given. Tungsten was, therefore, a tungstate of lime. Bergman, from its great weight, suspected that tungstic acid was in reality the oxide of a metal, and this conjecture was afterwards confirmed by the Elhuyarts, who extracted the same acid from wolfram, and succeeded in reducing it to the metallic state.
14. In 1782 and 1783 appeared his experiments on Prussian blue, in order to discover the nature of the colouring matter. These experiments were exceedingly numerous, and display uncommon ingenuity and sagacity. He succeeded in demonstrating that prussic acid, the name at that time given to the colouring principle, was a compound of carbon and azote. He pointed out a process for obtaining prussic acid in a separate state, and determined its properties. This paper threw at once a ray of light on one of the obscurest parts of chemistry. If he did not succeed in elucidating this difficult department completely, the fault must not be ascribed to him, but to the state of chemistry when his experiments were made; in fact, it would have been impossible to have gone further, till the nature of the different elastic fluids at that time under investigation had been thoroughly established. Perhaps in 1783 there was scarcely any other individual who could have carried this very difficult investigation so far as it was carried by Scheele.
15. In 1783 appeared his observations on the sweet principle of oils. He observed, that when olive oil and litharge are combined together, a sweet substance separates from the oil and floats on the surface. This substance, when treated with nitric acid, yields oxalic acid. It was therefore closely connected with sugar in its nature. He obtained the same sweet matter from linseed oil, oil of almonds, of rape-seed, from hogs' lard, and from butter. He therefore concluded that it was a principle contained in all the expressed or fixed oils.
16. In 1784 he pointed out a method by which citric acid may be obtained in a state of purity from lemon-juice. He likewise determined its characters, and showed that it was entitled to rank as a peculiar acid.
It was during the same year that he observed a white earthy matter, which may be obtained by washing rhubarb, in fine powder, with a sufficient quantity of water. This earthy matter he decomposed, and ascertained that it was a neutral salt, composed of oxalic acid, combined with lime. In a subsequent paper he showed, that the same oxalate of lime exists in a great number of roots of various plants.
17. In 1786 he showed that apples contain a peculiar acid, the properties of which he determined, and to which the name of malic acid has been given. In the same paper he examined all the common acid fruits of this country—gooseberries, currants, cherries, bilberries, &c., and determined the peculiar acids which they contain. Some owe their acidity to malic acid, some to citric acid, and some to tartaric acid; and not a few hold two, or even three, of these acids at the same time.
The same year he showed that the syderum of Bergman was phosphuret of iron, and the acidum perlatum of Proust biphosphate of soda.
The only other publication of Scheele, during 1785, was a short notice respecting a new mode of preparing magnesia alba. If sulphate of magnesia and common salt, both in solution, be mixed in the requisite proportions, a double decomposition takes place, and there will be formed sulphate of soda and muriate of magnesia. The greatest part of the former salt may be obtained out of the mixed ley by crystallization, and then the magnesia alba may be thrown down, from the muriate of magnesia, by means of an alkaline carbonate. The advantage of this new process is, the procuring of a considerable quantity of sulphate of soda in exchange for common salt, which is a much cheaper substance.
18. The last paper which Scheele published appeared in the Memoirs of the Stockholm Academy, for 1786: in it he gave an account of the characters of gallic acid, and the method of obtaining that acid from nutgalls.
Such is an imperfect sketch of the principal discoveries of Scheele. I have left out of view his controversial papers, which have now lost their interest; and a few others of minor importance, that this notice might not be extended beyond its due length. It will be seen that Scheele extended greatly the number of acids; indeed, he more than doubled the number of these bodies known when he began his chemical labours. The following acids were discovered by him; or, at least, it was he that first accurately pointed out their characters:
| Fluoric acid | Tartaric acid |
| Molybdic acid | Oxalic acid |
| Tungstic acid | Citric acid |
| Arsenic acid | Malic acid |
| Lactic acid | Saclactic |
| Gallic acid | Chlorine. |
To him, also, we owe the first knowledge of barytes, and of the characters of manganese. He determined the nature of the constituents of ammonia and prussic acid: he first determined the compound nature of common air, and the properties of the two elastic fluids of which it is composed. What other chemist, either a contemporary or predecessor of Scheele, can be brought in competition with him as a discoverer? And all was performed under the most unpropitious circumstances, and during the continuance of a very short life, for he died in the 44th year of his age.
CHAPTER III.
PROGRESS OF SCIENTIFIC CHEMISTRY IN FRANCE.
I have already given an account of the state of chemistry in France, during the earlier part of the eighteenth century, as it was cultivated by the Stahlian school. But the new aspect which chemistry put on in Britain in consequence of the discoveries of Black, Cavendish, and Priestley, and the conspicuous part which the gases newly made known was likely to take in the future progress of the science, drew to the study of chemistry, sometime after the middle of the eighteenth century, a man who was destined to produce a complete revolution, and to introduce the same precision, and the same accuracy of deductive reasoning which distinguishes the other branches of natural science. This man was Lavoisier.
Antoine Laurent Lavoisier was born in Paris on the 26th of August, 1743. His father being a man of opulence spared no expense on his education. His taste for the physical sciences was early displayed, and the progress which he made in them was uncommonly rapid. In the year 1764 a prize was offered by the French government for the best and most economical method of lighting the streets of an extensive city. Young Lavoisier, though at that time only twenty-one years of age, drew up a memoir on the subject which obtained the gold medal. This essay was inserted in the Memoirs of the French Academy of Sciences, for 1768. It was during that year, when he was only twenty-five years of age that he became a member of that scientific body. By this time he was become fully conscious of his own strength; but he hesitated for some time to which of the sciences he should devote his attention. He tried pretty early to determine, experimentally, some chemical questions which at that time drew the attention of practical chemists. For example: an elaborate paper of his appeared in the Memoirs of the French Academy, for 1768, on the composition of gypsum—a point at that time not settled; but which Lavoisier proved, as Margraaf had done before him, to be a compound of sulphuric acid and lime. In the Memoirs of the Academy, for 1770, two papers of his appeared, the object of which was to determine whether water could, as Margraaf had pretended, be converted into silica by long-continued digestion in glass vessels. Lavoisier found, as Margraaf stated, that when water is digested for a long time in a glass retort, a little silica makes its appearance; but he showed that this silica was wholly derived from the retort. Glass, it is well known, is a compound of silica and a fixed alkali. When water is long digested on it the glass is slightly corroded, a little alkali is dissolved in the water and a little silica separated in the form of a powder.
He turned a good deal of his attention also to geology, and made repeated journeys with Guettard into almost every part of France. The object in view was an accurate description of the mineralogical structure of France—an object accomplished to a considerable extent by the indefatigable exertions of Guettard, who published different papers on the subject in the Memoirs of the French Academy, accompanied with geological maps; which were at that time rare.
The mathematical sciences also engrossed a considerable share of his attention. In short he displayed no great predilection for one study more than another, but seemed to grasp at every branch of science with equal avidity. While in this state of suspension he became acquainted with the new and unexpected discoveries of Black, Cavendish, and Priestley, respecting the gases. This opened a new creation to his view, and finally determined him to devote himself to scientific chemistry.
In the year 1774 he published a volume under the title of "Essays Physical and Chemical." It was divided into two parts. The first part contained an historical detail of every thing that had been done on the subject of airs, from the time of Paracelsus down to the year 1774. We have the opinions and experiments of Van Helmont, Boyle, Hales, Boerhaave, Stahl, Venel, Saluces, Black, Macbride, Cavendish, and Priestley. We have the history of Meyer's acidum pingue, and the controversy carried on in Germany, between Jacquin on the one hand, and Crans and Smeth on the ether.
In the second part Lavoisier relates his own experiments upon gaseous substances. In the first four chapters he shows the truth of Dr. Black's theory of fixed air. In the 4th and 5th chapters he proves that when metallic calces are reduced, by heating them with charcoal, an elastic fluid is evolved, precisely of the same nature with carbonic acid gas. In the 6th chapter he shows that when metals are calcined their weight increases, and that a portion of air equal to their increase in weight is absorbed from the surrounding atmosphere. He observed that in a given bulk of air calcination goes on to a certain point and then stops altogether, and that air in which metals have been calcined does not support combustion so well as it did before any such process was performed in it. He also burned phosphorus in a given volume of air, observed the diminution of volume of the air and the increase of the weight of the phosphorus.
Nothing in these essays indicates the smallest suspicion that air was a mixture of two distinct fluids, and that only one of them was concerned in combustion and calcination; although this had been already deduced by Scheele from his own experiments, and though Priestley had already discovered the existence and peculiar properties of oxygen gas. It is obvious, however, that Lavoisier was on the way to make these discoveries, and had neither Scheele nor Priestley been fortunate enough to hit upon oxygen gas, it is exceedingly likely that he would himself have been able to have made that discovery.
Dr. Priestley, however, happened to be in Paris towards the end of 1774, and exhibited to Lavoisier, in his own laboratory in Paris, the method of procuring oxygen gas from red oxide of mercury. This discovery altered all his views, and speedily suggested not only the nature of atmospheric air, but also what happens during the calcination of metals and the combustion of burning bodies in general. These opinions when once formed he prosecuted with unwearied industry for more than twelve years, and after a vast number of experiments, conducted with a degree of precision hitherto unattempted in chemical investigations, he boldly undertook to disprove the existence of phlogiston altogether, and to explain all the phenomena hitherto supposed to depend upon that principle by the simple combination or separation of oxygen from bodies.
In these opinions he had for some years no coadjutors or followers, till, in 1785, Berthollet at a meeting of the Academy of Sciences, declared himself a convert. He was followed by M. Fourcroy, and soon after Guyton de Morveau, who was at that time the editor of the chemical department of the Encyclopédie Méthodique, was invited to Paris by Lavoisier and prevailed upon to join the same party. This was followed by a pretty vigorous controversy, in which Lavoisier and his associates gained a signal victory.
Lavoisier, after Buffon and Tillet, was treasurer to the academy, into the accounts of which he introduced both economy and order. He was consulted by the National Convention on the most eligible means of improving the manufacture of assignats, and of augmenting the difficulty of forging them. He turned his attention also to political economy, and between 1778 and 1785 he allotted 240 arpents in the Vendomois to experimental agriculture, and increased the ordinary produce by one-half. In 1791 the Constituent Assembly invited him to draw up a plan for rendering more simple the collection of the taxes, which produced an excellent report, printed under the title of "Territorial Riches of France."
In 1776 he was employed by Turgot to inspect the manufactory of gunpowder; which he made to carry 120 toises, instead of 90. It is pretty generally known, that during the war of the American revolution, the French gunpowder was much superior to the British; but it is perhaps not so generally understood, that for this superiority the French government were indebted to the abilities of Lavoisier. During the war of the French revolution, the quality of the powder of the two nations was reversed; the English being considerably superior to that of the French, and capable of carrying further. This was put to the test in a very remarkable way at Cadiz.
During the horrors of the dictatorship of Robespierre, Lavoisier began to suspect that he would be stripped of his property, and informed Lalande that he was extremely willing to work for his subsistence. It was supposed that he meant to pursue the profession of an apothecary, as most congenial to his studies: but he was accused, along with the other farmers-general, of defrauding the revenue, and thrown into prison. During that sanguinary period imprisonment and condemnation were synonymous terms. Accordingly, on the 8th of May, 1794, he suffered on the scaffold, with twenty-eight farmers-general, at the early age of fifty-one. It has been, alleged that Fourcroy, who at that time possessed considerable influence, might have saved him had he been disposed to have exerted himself. But this accusation has never been supported by any evidence. Lavoisier was a man of too much eminence to be overlooked, and no accused person at that time could be saved unless he was forgotten. A paper was presented to the tribunal, drawn up by M. Hallé, giving a catalogue of the works, and a recapitulation of the merits of Lavoisier; but it was thrown aside without even being read, and M. Hallé had reason to congratulate himself that his useless attempts to save Lavoisier did not terminate in his own destruction.
Lavoisier was tall, and possessed a countenance full of benignity, through which his genius shone forth conspicuous. He was mild, humane, sociable, obliging, and he displayed an incredible degree of activity. His influence was great, on account of his fortune, his reputation, and the place which he held in the treasury; but all the use which he made of it was to do good. His wife, whom he married in 1771, was Marie-Anna-Pierette-Paulze, daughter of a farmer-general, who was put to death at the same time with her husband; she herself was imprisoned, but saved by the fortunate destruction of the dictator himself, together with his abettors. It would appear that she was able to save a considerable part of her husband's fortune: she afterwards married Count Rumford, whom she survived.
Besides his volume of Physical and Chemical Essays, and his Elements of Chemistry, published in 1789, Lavoisier was the author of no fewer than sixty memoirs, which were published in the volumes of the Academy of Sciences, from 1772, to 1788, or in other periodical works of the time. I shall take a short review of the most important of these memoirs, dividing them into two parts: I. Those that are not connected with his peculiar chemical theory; II. Those which were intended to disprove the existence of phlogiston, and establish the antiphlogistic theory.
I. I have already mentioned his paper on gypsum, published in the Memoirs of the Academy, for 1768. He proves, by very decisive experiments, that this salt is a compound of sulphuric acid, lime, and water. But this had been already done by Margraaf, in a paper inserted into the Memoirs of the Berlin Academy, for 1750, entitled "An Examination of the constituent parts of the Stones that become luminous." The most remarkable circumstance attending this paper is, that an interval of eighteen years should elapse without Lavoisier's having any knowledge of this important paper of Margraaf; yet he quotes Pott and Cronstedt, who had written on the same subject later than Margraaf, at least Cronstedt. What makes this still more singular and unaccountable is, that a French translation of Margraaf's Opuscula had been published in Paris, in the year 1762. That a man in Lavoisier's circumstances, who, as appears from his paper, had paid considerable attention to chemistry, should not have perused the writings of one of the most eminent chemists that had ever existed, when they were completely within his power, constitutes, I think, one of the most extraordinary phenomena in the history of science.
2. If a want of historical knowledge appears conspicuous in Lavoisier's first chemical paper, the same remark cannot be applied to his second paper, "On the Nature of Water, and the Experiments by which it has been attempted to prove the possibility of changing it into Earth," which was inserted in the Memoirs of the French Academy, for 1770. This memoir is divided into two parts. In the first he gives a history of the progress of opinions on the subject, beginning with Van Helmont's celebrated experiment on the willow; then relating those of Boyle, Triewald, Miller, Eller, Gleditch, Bonnet, Kraft, Alston, Wallerius, Hales, Duhamel, Stahl, Boerhaave, Geoffroy, Margraaf, and Le Roy. This first part is interesting, in an historical point of view, and gives a very complete account of the progress of opinions upon the subject from the very first dawn of scientific chemistry down to his own time. There is, it is true, a remarkable difference between the opinions of his predecessors respecting the conversion of water into earth, and the experiments of Margraaf on the composition of selenite. The former were inaccurate, and were recorded by him that they might be refuted; but the experiments of Margraaf were accurate, and of the same nature with his own. The second part of this memoir contains his own experiments, made with much precision, which went to show that the earth was derived from the retort in which the experiments of Margraaf were made, and that we have no proof whatever that water may be converted into earth.
But these experiments of Lavoisier, though they completely disproved the inferences that Margraaf drew from his observations, by no means demonstrated that water might not be converted into different animal and vegetable substances by the processes of digestion. Indeed there can be no doubt that this is the case, and that the oxygen and hydrogen of which it is composed, enter into the composition of by far the greater number of animal and vegetable bodies produced by the action of the functions of living animals and vegetables. We have no evidence that the carbon, another great constituent of vegetable bodies, and the carbon and azote which constitute so great a proportion of animal substances, have their origin from water. They are probably derived from the food of plants and animals, and from the atmosphere which surrounds them, and which contains both of these principles in abundance.
Whether the silica, lime, alumina, magnesia, and iron, that exist in small quantity in plants, be derived from water and the atmosphere, is a question which we are still unable to answer. But the experiments of Schrader, which gained the prize offered by the Berlin Academy, in the year 1800, for the best essay on the following subject: To determine the earthy constituents of the different kinds of corn, and to ascertain whether these earthy parts are formed by the processes of vegetation, show at least that we cannot account for their production in any other way. Schrader analyzed the seeds of wheat, rye, barley, and oats, and ascertained the quantity of earthy matter which each contained. He then planted these different seeds in flowers of sulphur, and in oxides of antimony and zinc, watering them regularly with distilled water. They vegetated very well. He then dried the plants, and analyzed what had been the produce of a given weight of seed, and he found that the earthy matter in each was greater than it had been in the seeds from which they sprung. Now as the sulphur and oxides of zinc and antimony could furnish no earthy matter, no other source remains but the water with which the plants were fed, and the atmosphere with which they were surrounded. It may be said, indeed, that earthy matter is always floating about in the atmosphere, and that in this way they may have obtained all the addition of these principles which they contained. This is an objection not easily obviated, and yet it would require to be obviated before the question can be considered as answered.
3. Lavoisier's next paper, inserted in the Memoirs of the Academy, for 1771, was entitled "Calculations and Observations on the Project of the establishment of a Steam-engine to supply Paris with Water." This memoir, though long and valuable, not being strictly speaking chemical, I shall pass over. Mr. Watt's improvements seem to have been unknown to Lavoisier, indeed as his patent was only taken out in 1769, and as several years elapsed before the merits of his new steam-engine became generally known, Lavoisier's acquaintance with it in 1771 could hardly be expected.
4. In 1772 we find a paper, by Lavoisier, in the Memoirs of the Academy, "On the Use of Spirit of Wine in the analysis of Mineral Waters." He shows how the earthy muriates may be separated from the sulphates by digesting the mixed mass in alcohol. This process no doubt facilitates the separation of the salts from each other: but it is doubtful whether the method does not occasion new inaccuracies that more than compensate the facility of such separations. When different salts are dissolved in water in small quantities, it may very well happen that they do not decompose each other, being at too great a distance from each other to come within the sphere of mutual action. Thus it is possible that sulphate of soda and muriate of lime may exist together in the same water. But if we concentrate this water very much, and still more, if we evaporate to dryness, the two salts will gradually come into the sphere of mutual action, a double decomposition will take place, and there will be formed sulphate of lime and common salt. If upon the dry residue we pour as much distilled water as was driven off by the evaporation, we shall not be able to dissolve the saline matter deposited; a portion of sulphate of lime will remain in the state of a powder. Yet before the evaporation, all the saline contents of the water were in solution, and they continued in solution till the water was very much concentrated. This is sufficient to show that the nature of the salts was altered by the evaporation. If we digest the dry residue in spirit of wine, we may dissolve a portion of muriate of lime, if the quantity of that salt in the original water was greater than the sulphate of soda was capable of decomposing: but if the quantity was just what the sulphate of soda could decompose, the alcohol will dissolve nothing, if it be strong enough, or nothing but a little common salt, if its specific gravity was above 0·820. We cannot, therefore, depend upon the salts which we obtain after evaporating a mineral water to dryness, being the same as those which existed in the mineral water itself. The nature of the salts must always be determined some other way.
5. In the Memoirs of the Academy, for 1772 (published in 1776), are inserted two elaborate papers of Lavoisier, on the combustion of the diamond. The combustibility of the diamond was suspected by Newton, from its great refractive power. His suspicion was confirmed in 1694, by Cosmo III., Grand Duke of Tuscany, who employed Averani and Targioni to try the effect of powerful burning-glasses upon diamonds. They were completely dissipated by the heat. Many years after, the Emperor Francis I. caused various diamonds to be exposed to the heat of furnaces. They also were dissipated, without leaving any trace behind them. M. Darcet, professor of chemistry at the Royal College of Paris, being employed with Count Lauragais in a set of experiments on the manufacture of porcelain, took the opportunity of trying what effect the intense heat of the porcelain furnaces produced upon various bodies. Diamonds were not forgotten. He found that they were completely dissipated by the heat of the furnace, without leaving any traces behind them. Darcet found that a violent heat was not necessary to volatilize diamonds. The heat of an ordinary furnace was quite sufficient. In 1771 a diamond, belonging to M. Godefroi Villetaneuse, was exposed to a strong heat by Macquer. It was placed upon a cupel, and raised to a temperature high enough to melt copper. It was observed to be surrounded with a low red flame, and to be more intensely red than the cupel. In short, it exhibited unequivocal marks of undergoing real combustion.
These experiments were soon after repeated by Lavoisier before a large company of men of rank and science. The real combustion of the diamond was established beyond doubt; and it was ascertained also, that if it be completely excluded from the air, it may be exposed to any temperature that can be raised in a furnace without undergoing any alteration. Hence it is clear that the diamond is not a volatile substance, and that it is dissipated by heat, not by being volatilized, but by being burnt.
The object of Lavoisier in his experiments was to determine the nature of the substance into which the diamond was converted by burning. In the first part he gives as usual a history of every thing which had been done previous to his own experiments on the combustion of the diamond. In the second part we have the result of his own experiments upon the same subject. He placed diamonds on porcelain supports in glass jars standing inverted over water and over mercury; and filled with common air and with oxygen gas.[4]
The diamonds were consumed by means of burning-glasses. No water or smoke or soot made their appearance, and no alteration took place on the bulk of the air when the experiments were made over mercury. When they were made over water, the bulk of the air was somewhat diminished. It was obvious from this that diamond when burnt in air or oxygen gas, is converted into a gaseous substance, which is absorbed by water. On exposing air in which diamond had been burnt, to lime-water, a portion of it was absorbed, and the lime-water was rendered milky. From this it became evident, that when diamond is burnt, carbonic acid is formed, and this was the only product of the combustion that could be discovered.
Lavoisier made similar experiments with charcoal, burning it in air and oxygen gas, by means of a burning-glass. The results were the same: carbonic acid gas was formed in abundance, and nothing else. These experiments might have been employed to support and confirm Lavoisier's peculiar theory, and they were employed by him for that purpose afterwards. But when they were originally published, no such intention appeared evident; though doubtless he entertained it.
6. In the second volume of the Journal de Physique, for 1772, there is a short paper by Lavoisier on the conversion of water into ice. M. Desmarets had given the academy an account of Dr. Black's experiments, to determine the latent heat of water. This induced Lavoisier to relate his experiments on the same subject. He does not inform us whether they were made in consequence of his having become acquainted with Dr. Black's theory, though there can be no doubt that this must have been the case. The experiments related in this short paper are not of much consequence. But I have thought it worth while to notice it because it authenticates a date at which Lavoisier was acquainted with Dr. Black's theory of latent heat.
7. In the third volume of the Journal de Physique, there is an account of a set of experiments made by Bourdelin, Malouin, Macquer, Cadet, Lavoisier, and Baumé on the white-lead ore of Pullowen. The report is drawn up by Baumé. The nature of the ore is not made out by these experiments. They were mostly made in the dry way, and were chiefly intended to show that the ore was not a chloride of lead. It was most likely a phosphate of lead.
8. In the Memoirs of the Academy, for 1774, we have the experiments of Trudaine, de Montigny, Macquer, Cadet, Lavoisier, and Brisson, with the great burning-glass of M. Trudaine. The results obtained cannot be easily abridged, and are not of sufficient importance to be given in detail.
9. Analysis of some waters brought from Italy by M. Cassini, junior. This short paper appeared in the Memoirs of the Academy, for 1777. The waters in question were brought from alum-pits, and were found to contain alum and sulphate of iron.
10. In the same volume of the Memoirs of the Academy, appeared his paper "On the Ash employed by the Saltpetre-makers of Paris, and on its use in the Manufacture of Saltpetre." This is a curious and valuable paper; but not sufficiently important to induce me to give an abstract of it here.
11. In the Memoirs of the Academy, for 1777, appeared an elaborate paper, by Lavoisier, "On the Combination of the matter of Fire, with Evaporable Fluids, and the Formation of Elastic aeriform Fluids." In this paper he adopts precisely the same theory as Dr. Black had long before established. It is remarkable that the name of Dr. Black never occurs in the whole paper, though we have seen that Lavoisier had become acquainted with the doctrine of latent heat, at least as early as the year 1772, as he mentioned the circumstance in a short paper inserted that year in the Journal de Physique, and previously read to the academy.
12. In the same volume of the Memoirs of the Academy, we have a paper entitled "Experiments made by Order of the Academy, on the Cold of the year 1775, by Messrs. Bezout, Lavoisier, and Vandermond." It is sufficiently known that the beginning of the year 1776 was distinguished in most parts of Europe by the weather. The object of this paper, however, is rather to determine the accuracy of the different thermometers at that time used in France, than to record the lowest temperature which had been observed. It has some resemblance to a paper drawn up about the same time by Mr. Cavendish, and published in the Philosophical Transactions.
13. In the Memoirs of the Academy, for 1778, appeared a paper entitled "Analysis of the Waters of the Lake Asphaltes, by Messrs. Macquer, Lavoisier, and Sage." This water is known to be saturated with salt. It is needless to state the result of the analysis contained in this paper, because it is quite inaccurate. Chemical analysis had not at that time made sufficient progress to enable chemists to analyze mineral waters with precision.
The observation of Lavoisier and Guettard, which appeared at the same time, on a species of steatite, which is converted by the fire into a fine biscuit of porcelain, and on two coal-mines, the one in Franche-Comté, the other in Alsace, do not require to be particularly noticed.
14. In the Mem. de l'Académie, for 1780 (published in 1784), we have a paper, by Lavoisier, "On certain Fluids which may be obtained in an aeriform State, at a degree of Heat not much higher than the mean Temperature of the Earth." These fluids are sulphuric ether, alcohol, and water. He points out the boiling temperature of these liquids, and shows that at that temperature the vapour of these bodies possesses the elasticity of common air, and is permanent as long as the high temperature continues. He burnt a mixture of vapour of ether and oxygen gas, and showed that during the combustion carbonic acid gas is formed. Lavoisier's notions respecting these vapours, and what hindered the liquids at the boiling temperature from being all converted into vapour were not quite correct. Our opinions respecting steam and vapours in general were first rectified by Mr. Dalton.
15. In the Mem. de l'Académie, for 1780, appeared also the celebrated paper on heat, by Lavoisier and Laplace. The object of this paper was to determine the specific heat of various bodies, and to investigate the proposals that had been made by Dr. Irvine for determining the point at which a thermometer would stand, if plunged into a body destitute of heat. This point is usually called the real zero. They begin by describing an instrument which they had contrived to measure the quantity of heat which leaves a body while it is cooling a certain number of degrees. To this instrument they gave the name of calorimeter. It consisted of a kind of hollow, surrounded on every side by ice. The hot body was put into the centre. The heat which it gave out while cooling was all expended in melting the ice, which was of the temperature of 32°, and the quantity of heat was proportional to the quantity of ice melted. Hence the quantity of ice melted, while equal weights of hot bodies were cooling a certain number of degrees, gave the direct ratios of the specific heats of each. In this way they obtained the following specific heats:
| Specific heat. | |
| Water | 1 |
| Sheet-iron | 0·109985 |
| Glass without lead (crystal) | 0·1929 |
| Mercury | 0·029 |
| Quicklime | 0·21689 |
| Mixture of 9 water with 16 lime | 0·439116 |
| Sulphuric acid of 1·87058 | 0·334597 |
| 4 sulphuric acid, 3 water | 0·603162 |
| 4 sulphuric acid, 5 water | 0·663102 |
| Nitric acid of 1·29895 | 0·661391 |
| 9⅓ nitric acid, 1 lime | 0·61895 |
| 1 saltpetre, 8 water | 0·8167 |
Their experiments were inconsistent with the conclusions drawn by Dr. Irvine, respecting the real zero, from the diminution of the specific heat, and the heat evolved when sulphuric acid was mixed with various proportions of water, &c. If the experiments of Lavoisier and Laplace approached nearly to accuracy, or, indeed, unless they were quite inaccurate, it is obvious that the conclusions of Irvine must be quite erroneous. It is remarkable that though the experiments of Crawford, and likewise those of Wilcke, and of several others, on specific heat had been published before this paper made its appearance, no allusion whatever is made to these publications. Were we to trust to the information communicated in the paper, the doctrine of specific heat originated with Lavoisier and Laplace. It is true that in the fourth part of the paper, which treats of combustion and respiration, Dr. Crawford's, theory of animal heat is mentioned, showing clearly that our authors were acquainted with his book on the subject. And, as this theory is founded on the different specific heats of bodies, there could be no doubt that he was acquainted with that doctrine.
16. In the Mem. de l'Académie, for 1780, occur the two following memoirs:
Report made to the Royal Academy of Sciences on the Prisons. By Messrs. Duhamel, De Montigny, Le Roy, Tenon, Tillet, and Lavoisier.
Report on the Process for separating Gold and Silver. By Messrs. Macquer, Cadet, Lavoisier, Baumé, Cornette, and Berthollet.
17. In the Mem. de l'Académie, for 1781, we find a memoir by Lavoisier and Laplace, on the electricity evolved when bodies are evaporated or sublimed. The result of these experiments was, that when water was evaporated electricity was always evolved. They concluded from these observations, that whenever a body changes its state electricity is always evolved. But when Saussure attempted to repeat these observations, he could not succeed. And, from the recent experiments of Pouillet, it seems to follow that electricity is evolved only when bodies undergo chemical decomposition or combination. Such experiments depend so much upon very minute circumstances, which are apt to escape the attention of the observer, that implicit confidence cannot be put in them till they have been often repeated, and varied in every possible manner.
18. In the Memoires de l'Académie, for 1781, there is a paper by Lavoisier on the comparative value of the different substances employed as articles of fuel. The substances compared to each other are pit-coal, coke, charcoal, and wood. It would serve no purpose to state the comparison here, as it would not apply to this country; nor, indeed, would it at present apply even to France.
We have, in the same volume, his paper on the mode of illuminating theatres.
19. In the Memoires de l'Académie, for 1782 (printed in 1785), we have a paper by Lavoisier on a method of augmenting considerably the action of fire and of heat. The method which he proposes is a jet of oxygen gas, striking against red-hot charcoal. He gives the result of some trials made in this way. Platinum readily melted. Pieces of ruby or sapphire were softened sufficiently to run together into one stone. Hyacinth lost its colour, and was also softened. Topaz lost its colour, and melted into an opaque enamel. Emeralds and garnets lost their colour, and melted into opaque coloured glasses. Gold and silver were volatilized; all the other metals, and even the metallic oxides, were found to burn. Barytes also burns when exposed to this violent heat. This led Lavoisier to conclude, as Bergman had done before him, that Barytes is a metallic oxide. This opinion has been fully verified by modern chemists. Both silica and alumina were melted. But he could not fuse lime nor magnesia. We are now in possession of a still more powerful source of heat in the oxygen and hydrogen blowpipe, which is capable of fusing both lime and magnesia, and, indeed, every substance which can be raised to the requisite heat without burning or being volatilized. This subject was prosecuted still further by Lavoisier in another paper inserted in a subsequent volume of the Memoires de l'Académie. He describes the effect on rock-crystal, quartz, sandstone, sand, phosphorescent quartz, milk quartz, agate, chalcedony, cornelian, flint, prase, nephrite, jasper, felspar, &c.
20. In the same volume is inserted a memoir "On the Nature of the aeriform elastic Fluids which are disengaged from certain animal Substances in a state of Fermentation." He found that a quantity of recent human fæces, amounting to about five cubic inches, when kept at a temperature approaching to 60° emitted, every day for a month, about half a cubic inch of gas. This gas was a mixture of eleven parts carbonic acid gas, and one part of an inflammable gas, which burnt with a blue flame, and was therefore probably carbonic oxide. Five cubic inches of old human fæces from a necessary kept in the same temperature, during the first fifteen days emitted about a third of a cubic inch of gas each day; and during each of the second fifteen days, about one fourth of a cubic inch. This gas was a mixture of thirty-eight volumes of carbonic acid gas, and sixty-two volumes of a combustible gas, burning with a blue flame, and probably carbonic oxide.
Fresh fæces do not effervesce with dilute sulphuric acid, but old moist fæces do, and emit about eight times their volume of carbonic acid gas. Quicklime, or caustic potash, mixed with fæces, puts a stop to the evolution of gas, doubtless by preventing all fermentation. During effervescence of fæcal matter the air surrounding it is deprived of a little of its oxygen, probably in consequence of its combining with the nascent inflammable gas which is slowly disengaged.
II. We come now to the new theory of combustion of which Lavoisier was the author, and upon which his reputation with posterity will ultimately depend. Upon this subject, or at least upon matters more or less intimately connected with it, no fewer than twenty-seven memoirs of his, many of them of a very elaborate nature, and detailing expensive and difficult experiments, appeared in the different volumes of the academy between 1774 and 1788. The analogy between the combustion of bodies and the calcination of metals had been already observed by chemists, and all admitted that both processes were owing to the same cause; namely, the emission of phlogiston by the burning or calcining body. The opinion adopted by Lavoisier was, that during burning and calcination nothing whatever left the bodies, but that they simply united with a portion of the air of the atmosphere. When he first conceived this opinion he was ignorant of the nature of atmospheric air, and of the existence of oxygen gas. But after that principle had been discovered, and shown to be a constituent of atmospherical air, he soon recognised that it was the union of oxygen with the burning and calcining body that occasioned the phenomena. Such is the outline of the Lavoisierian theory stated in the simplest and fewest words. It will be requisite to make a few observations on the much-agitated question whether this theory originated with him.
It is now well known that John Rey, a physician at Bugue, in Perigord, published a book in 1630, in order to explain the cause of the increase of weight which lead and tin experience during their calcination. After refuting in succession all the different explanations of this increase of weight which had been advanced, he adds, "To this question, then, supported on the grounds already mentioned, I answer, and maintain with confidence, that the increase of weight arises from the air, which is condensed, rendered heavy and adhesive by the violent and long-continued heat of the furnace. This air mixes itself with the calx (frequent agitation conducing), and attaches itself to the minutest molecules, in the same manner as water renders heavy sand which is agitated with it, and moistens and adheres to the smallest grains." There cannot be the least doubt from this passage that Rey's opinion was precisely the same as the original one of Lavoisier, and had Lavoisier done nothing more than merely state in general terms that during calcination air unites with the calcining bodies, it might have been suspected that he had borrowed his notions from those of Rey. But the discovery of oxygen, and the numerous and decisive proofs which he brought forward that during burning and calcination oxygen unites with the burning and calcining body, and that this oxygen may be again separated and exhibited in its original elastic state oblige us to alter our opinion. And whether we admit that he borrowed his original notion from Rey, or that it suggested itself to his own mind, the case will not be materially altered. For it is not the man who forms the first vague notion of a thing that really adds to the stock of our knowledge, but he who demonstrates its truth and accurately determines its nature.
Rey's book and his opinions were little known. He had not brought over a single convert to his doctrine, a sufficient proof that he had not established it by satisfactory evidence. We may therefore believe Lavoisier's statement, when he assures us that when he first formed his theory he was ignorant of Rey, and never had heard that any such book had been published.
The theory of combustion advanced by Dr. Hook, in 1665, in his Micrographia, approaches still nearer to that of Lavoisier than the theory of Rey, and indeed, so far as he has explained it, the coincidence is exact. According to Hook there exists in common air a certain substance which is like, if not the very same with that which is fixed in saltpetre. This substance has the property of dissolving all combustibles; but only when their temperature is sufficiently raised. The solution takes place with such rapidity that it occasions fire, which in his opinion is mere motion. The dissolved substance may be in the state of air, or coagulated in a liquid or solid form. The quantity of this solvent in a given bulk of air is incomparably less than in the same bulk of saltpetre. Hence the reason why a combustible continues burning but a short time in a given bulk of air: the solvent is soon saturated, and then of course the combustion is at an end. This explains why combustion requires a constant supply of fresh air, and why it is promoted by forcing in air with bellows. Hook promised to develop this theory at greater length in a subsequent work; but he never fulfilled his promise; though in his Lampas, published about twelve years afterwards, he gives a beautiful chemical explanation of flame, founded on the very same theory.
From the very general terms in which Hook expresses himself, we cannot judge correctly of the extent of his knowledge. This theory, so far as it goes, coincides exactly with our present notions on the subject. His solvent is oxygen gas, which constitutes one-fifth part of the volume of the air, but exists in much greater quantity in saltpetre. It combines with the burning body, and the compound formed may either be a gas, a liquid, or a solid, according to the nature of the body subjected to combustion.
Lavoisier nowhere alludes to this theory of Hook nor gives the least hint that he had ever heard of it. This is the more surprising, because Hook was a man of great celebrity; and his Micrographia, as containing the original figures and descriptions of many natural objects, is well known, not merely in Great Britain, but on the continent. At the same time it must be recollected that Hook's theory is supported by no evidence; that it is a mere assertion, and that nobody adopted it. Even then, if we were to admit that Lavoisier was acquainted with this theory, it would derogate very little from his merit, which consisted in investigating the phenomena of combustion and calcination, and in showing that oxygen became a constituent of the burnt and calcined bodies.
About ten years after the publication of the Micrographia, Dr. Mayow, of Oxford, published his Essays. In the first of which, De Sal-nitro et Spiritu Nitro-aëreo, he obviously adopts Dr. Hook's theory of combustion, and he applies it with great ingenuity to explain the nature of respiration. Dr. Mayow's book had been forgotten when the attention of men of science was attracted to it by Dr. Beddoes. Dr. Yeats, of Bedford, published a very interesting work on the merits of Mayow, in 1798. It will be admitted at once by every person who takes the trouble of perusing Mayow's tract, that he was not satisfied with mere theory; but proved by actual experiment that air was absorbed during combustion, and altered during respiration. He has given figures of his apparatus, and they are very much of the same nature with those afterwards made use of by Lavoisier. It would be wrong, therefore, to deprive Mayow of the reputation to which he is entitled for his ingeniously-contrived and well-executed experiments. It must be admitted that he proved both the absorption of air during combustion and respiration; but even this does not take much from the fair fame of Lavoisier. The analysis of air and the discovery of oxygen gas really diminish the analogy between the theories of Mayow and Lavoisier, or at any rate the full investigation of the subject and the generalization of it belong exclusively to Lavoisier.
Attempts were made by the other French chemists, about the beginning of the revolution, to associate themselves with Lavoisier, as equally entitled with himself to the merit of the antiphlogistic theory; but Lavoisier himself has disclaimed the partnership. Some years before his death, he had formed the plan of collecting together all his papers relating to the antiphlogistic theory and publishing them in one work; but his death interrupted the project. However, his widow afterwards published the first two volumes of the book, which were complete at the time of his death. In one of these volumes Lavoisier claims for himself the exclusive discovery of the cause of the augmentation of weight which bodies undergo during combustion and calcination. He informs us that a set of experiments, which he made in 1772, upon the different kinds of air which are disengaged in effervescence, and a great number of other chemical operations discovered to him demonstratively the cause of the augmentation of weight which metals experience when exposed to heat. "I was young," says he, "I had newly entered the lists of science, I was desirous of fame, and I thought it necessary to take some steps to secure to myself the property of my discovery. At that time there existed an habitual correspondence between the men of science of France and those of England. There was a kind of rivality between the two nations, which gave importance to new experiments, and which sometimes was the cause that the writers of the one or the other of the nations disputed the discovery with the real author. Consequently, I thought it proper to deposit on the 1st of November, 1772, the following note in the hands of the secretary of the academy. This note was opened on the 1st of May following, and mention of these circumstances marked at the top of the note. It was in the following terms:
"About eight days ago I discovered that sulphur in burning, far from losing, augments in weight; that is to say, that from one pound of sulphur much more than one pound of vitriolic acid is obtained, without reckoning the humidity of the air. Phosphorus presents the same phenomenon. This augmentation of weight arises from a great quantity of air, which becomes fixed during the combustion, and which combines with the vapours.
"This discovery, which I confirmed by experiments which I regard as decisive, led me to think that what is observed in the combustion of sulphur and phosphorus, might likewise take place with respect to all the bodies which augment in weight by combustion and calcination; and I was persuaded that the augmentation of weight in the calces of metals proceeded from the same cause. The experiment fully confirmed my conjectures. I operated the reduction of litharge in close vessels with Hales's apparatus, and I observed, that at the moment of the passage of the calx into the metallic state, there was a disengagement of air in considerable quantity, and that this air formed a volume at least one thousand times greater than that of the litharge employed. As this discovery appears to me one of the most interesting which has been made since Stahl, I thought it expedient to secure to myself the property, by depositing the present note in the hands of the secretary of the academy, to remain secret till the period when I shall publish my experiments.
"Lavoisier.
"Paris, November 11, 1772."
This note leaves no doubt that Lavoisier had conceived his theory, and confirmed it by experiment, at least as early as November, 1772. But at that time the nature of air and the existence of oxygen were unknown. The theory, therefore, as he understood it at that time, was precisely the same as that of John Rey. It was not till the end of 1774 that his views became more precise, and that he was aware that oxygen is the portion of the air which unites with bodies during combustion, and calcination.
Nothing can be more evident from the whole history of the academy, and of the French chemists during this eventful period, for the progress of the science, that none of them participated in the views of Lavoisier, or had the least intention of giving up the phlogistic theory. It was not till 1785, after his experiments had been almost all published, and after all the difficulties had been removed by the two great discoveries of Mr. Cavendish, that Berthollet declared himself a convert to the Lavoisierian opinions. This was soon followed by others, and within a very few years almost all the chemists and men of science in France enlisted themselves on the same side. Lavoisier's objection, then, to the phrase La Chimie Française, is not without reason, the term Lavoisierian Chemistry should undoubtedly be substituted for it. This term, La Chimie Française was introduced by Fourcroy. Was Fourcroy anxious to clothe himself with the reputation of Lavoisier, and had this any connexion with the violent death of that illustrious man?
The first set of experiments which Lavoisier published on his peculiar views, was entitled, "A Memoir on the Calcination of Tin in close Vessels; and on the Cause of the increase of Weight which the Metal acquires during this Process." It appeared in the Memoirs of the Academy, for 1774. In this paper he gives an account of several experiments which he had made on the calcination of tin in glass retorts, hermetically sealed. He put a quantity of tin (about half a pound) into a glass retort, sometimes of a larger and sometimes of a smaller size, and then drew out the beak into a capillary tube. The retort was now placed upon the sand-bath, and heated till the tin just melted. The extremity of the capillary beak of the retort was now fused so as to seal it hermetically. The object of this heating was to prevent the retort from bursting by the expansion of the air during the process. The retort, with its contents, was now carefully weighed, and the weight noted. It was put again on the sand-bath, and kept melted till the process of calcination refused to advance any further. He observed, that if the retort was small, the calcination always stopped sooner than it did if the retort was large. Or, in other words, the quantity of tin calcined was always proportional to the size of the retort.
After the process was finished, the retort (still hermetically sealed) was again weighed, and was always found to have the same weight exactly as at first. The beak of the retort was now broken off, and a quantity of air entered with a hissing noise. The increase of weight was now noted: it was obviously owing to the air that had rushed in. The weight of air that had been at first driven out by the fusion of the tin had been noted, and it was now found that a considerably greater quantity had entered than had been driven out at first. In some experiments, as much as 10·06 grains, in others 9·87 grains, and in some less than this, when the size of the retort was small. The tin in the retort was mostly unaltered, but a portion of it had been converted into a black powder, weighing in some cases above two ounces. Now it was found in all cases, that the weight of the tin had increased, and the increase of weight was always exactly equal to the diminution of weight which the air in the retort had undergone, measured by the quantity of new air which rushed in when the beak of the retort was broken, minus the air that had been driven out when the tin was originally melted before the retort was hermetically sealed.
Thus Lavoisier proved by these first experiments, that when tin is calcined in close vessels a portion of the air of the vessel disappears, and that the tin increases in weight just as much as is equivalent to the loss of weight which the air has sustained. He therefore inferred, that this portion of air had united with the tin, and that calx of tin is a compound of tin and air. In this first paper there is nothing said about oxygen, nor any allusion to lead to the suspicion that air is a compound of different elastic fluids. These, therefore, were probably the experiments to which Lavoisier alludes in the note which he lodged with the secretary of the academy in November, 1772.
He mentions towards the end of the Memoir that he had made similar experiments with lead; but he does not communicate any of the numerical results: probably because the results were not so striking as those with tin. The heat necessary to melt lead is so high that satisfactory experiments on its calcination could not easily be made in a glass retort.
Lavoisier's next Memoir appeared in the Memoirs of the Academy, for 1775, which were published in 1778. It is entitled, "On the Nature of the Principle which combines with the Metals during their Calcination, and which augments their Weight." He observes that when the metallic calces are reduced to the metallic state it is found necessary to heat them along with charcoal. In such cases a quantity of carbonic acid gas is driven off, which he assures us is the charcoal united to the elastic fluid contained in the calx. He tried to reduce the calx of iron by means of burning-glasses, while placed under large glass receivers standing over mercury; but as the gas thus evolved was mixed with a great deal of common air which was necessarily left in the receiver, he was unable to determine its nature. This induced him to have recourse to red oxide of mercury. He showed in the first place that this substance (mercurius præcipitatus per se) was a true calx, by mixing it with charcoal powder in a retort and heating it. The mercury was reduced and abundance of carbonic acid gas was collected in an inverted glass jar standing in a water-cistern into which the beak of the retort was plunged. On heating the red oxide of mercury by itself it was reduced to the metallic state, though not so easily, and at the same time a gas was evolved which possessed the following properties:
1. It did not combine with water by agitation.
2. It did not precipitate lime-water.
3. It did not unite with fixed or volatile alkalies.
4. It did not at all diminish their caustic quality.
5. It would serve again for the calcination of metals.
6. It was diminished like common air by addition of one-third of nitrous gas.
7. It had none of the properties of carbonic acid gas. Far from being fatal, like that gas, to animals, it seemed on the contrary more proper for the purposes of respiration. Candles and burning bodies were not only not extinguished by it, but burned with an enlarged flame in a very remarkable manner. The light they gave was much greater and clearer than in common air.
He expresses his opinion that the same kind of air would be obtained by heating nitre without addition, and this opinion is founded on the fact that when nitre is detonated with charcoal it gives out abundance of carbonic acid gas.
Thus Lavoisier shows in this paper that the kind of air which unites with metals during their calcination is purer and fitter for combustion than common air. In short it is the gas which Dr. Priestley had discovered in 1774, and which is now known by the name of oxygen gas.
This Memoir deserves a few animadversions. Dr. Priestley discovered oxygen gas in August, 1774; and he informs us in his life, that in the autumn of that year he went to Paris and exhibited to Lavoisier, in his own laboratory the mode of obtaining oxygen gas by heating red oxide of mercury in a gun-barrel, and the properties by which this gas is distinguished—indeed the very properties which Lavoisier himself enumerates in his paper. There can, therefore, be no doubt that Lavoisier was acquainted with oxygen gas in 1774, and that he owed his knowledge of it to Dr. Priestley.
There is some uncertainty about the date of Lavoisier's paper. In the History of the Academy, for 1775, it is merely said about it, "Read at the resumption (rentrée) of the Academy, on the 26th of April, by M. Lavoisier," without naming the year. But it could not have been before 1775, because that is the year upon the volume of the Memoirs; and besides, we know from the Journal de Physique (v. 429), that 1775 was the year on which the paper of Lavoisier was read.
Yet in the whole of this paper the name of Dr. Priestley never occurs, nor is the least hint given that he had already obtained oxygen gas by heating red oxide of mercury. So far from it, that it is obviously the intention of the author of the paper to induce his readers to infer that he himself was the discoverer of oxygen gas. For after describing the process by which oxygen gas was obtained by him, he says nothing further remained but to determine its nature, and "I discovered with much surprise that it was not capable of combination with water by agitation," &c. Now why the expression of surprise in describing phenomena which had been already shown? And why the omission of all mention of Dr. Priestley's name? I confess that this seems to me capable of no other explanation than a wish to claim for himself the discovery of oxygen gas, though he knew well that that discovery had been previously made by another.
The next set of experiments made by Lavoisier to confirm or extend his theory, was "On the Combustion of Phosphorus, and the Nature of the Acid which results from that Combustion." It appeared in the Memoirs of the Academy, for 1777. The result of these experiments was very striking. When phosphorus is burnt in a given bulk of air in sufficient quantity, about four-fifths of the volume of the air disappears and unites itself with the phosphorus. The residual portion of the air is incapable of supporting combustion or maintaining animal life. Lavoisier gave it the name of mouffette atmospherique, and he describes several of its properties. The phosphorus by combining with the portion of air which has disappeared, is converted into phosphoric acid, which is deposited on the inside of the receiver in which the combustion is performed, in the state of fine white flakes. One grain by this process is converted into two and a half grains of phosphoric acid. These observations led to the conclusion that atmospheric air is a mixture or compound of two distinct gases, the one (oxygen) absorbed by burning phosphorus, the other (azote) not acted on by that principle, and not capable of uniting with or calcining metals. These conclusions had already been drawn by Scheele from similar experiments, but Lavoisier was ignorant of them.
In the second part of this paper, Lavoisier describes the properties of phosphoric acid, and gives an account of the salts which it forms with the different bases. The account of these salts is exceedingly imperfect, and it is remarkable that Lavoisier makes no distinction between phosphate of potash and phosphate of soda; though the different properties of these two salts are not a little striking. But these were not the investigations in which Lavoisier excelled.
The next paper in which the doctrines of the antiphlogistic theory were still further developed, was inserted in the Memoirs of the Academy, for 1777. It is entitled, "On the Combustion of Candles in atmospherical Air, and in Air eminently Respirable." This paper is remarkable, because in it he first notices Dr. Priestley's discovery of oxygen gas; but without any reference to the preceding paper, or any apology for not having alluded in it to the information which he had received from Dr. Priestley.
He begins by saying that it is necessary to distinguish four different kinds of air. 1. Atmospherical air in which we live, and which we breath. 2. Pure air (oxygen), alone fit for breathing, constituting about the fourth of the volume of atmospherical air, and called by Dr. Priestley dephlogisticated air. 3. Azotic gas, which constitutes about three-fourths of the volume of atmospherical air, and whose properties are still unknown. 4. Fixed air, which he proposed to call (as Bucquet had done) acide crayeux, acid of chalk.
In this paper Lavoisier gives an account of a great many trials that he made by burning candles in given volumes of atmospherical air and oxygen gas enclosed in glass receivers, standing over mercury. The general conclusion which he deduces from these experiments are—that the azotic gas of the air contributes nothing to the burning of the candle; but the whole depends upon the oxygen gas of the air, constituting in his opinion one-fourth of its volume; that during the combustion of a candle in a given volume of air only two-fifths of the oxygen are converted into carbonic acid gas, while the remaining three-fifths remain unaltered; but when the combustion goes on in oxygen gas a much greater proportion (almost the whole) of this gas is converted into carbonic acid gas. Finally, that phosphorus, when burnt in air acts much more powerfully on the oxygen of the air than a lighted candle, absorbing four-fifths of the oxygen and converting it into phosphoric acid.
It is evident that at the time this paper was written, Lavoisier's theory was nearly complete. He considered air as a mixture of three volumes of azotic gas, and one volume of oxygen gas. The last alone was concerned in combustion and calcination. During these processes a portion of the oxygen united with the burning body, and the compound formed constituted the acid or the calx. Thus he was able to account for combustion and calcination without having recourse to phlogiston. It is true that several difficulties still lay in his way, which he was not yet able to obviate, and which prevented any other person from adopting his opinions. One of the greatest of these was the fact that hydrogen gas was evolved during the solution of several metals in dilute sulphuric or muriatic acid; that by this solution these metals were converted into calces, and that calces, when heated in hydrogen gas, were reduced to the metallic state while the hydrogen disappeared. The simplest explanation of these phenomena was the one adopted by chemists at the time. Hydrogen was considered as phlogiston. By dissolving metals in acids, the phlogiston was driven off and the calx remained: by heating the calx in hydrogen, the phlogiston was again absorbed and the calx reduced to the metallic state.
This explanation was so simple and appeared so satisfactory, that it was universally adopted by chemists with the exception of Lavoisier himself. There was a circumstance, however, which satisfied him that this explanation, however plausible, was not correct. The calx was heavier than the metal from which it had been produced. And hydrogen, though a light body, was still possessed of weight. It was obviously impossible, then, that the metal could be a combination of the calx and hydrogen. Besides, he had ascertained by direct experiment, that the calces of mercury, tin, and lead are compounds of the respective metals and oxygen. And it was known that when the other calces were heated with charcoal, they were reduced to the metallic state, and at the same time carbonic acid gas is evolved. The very same evolution takes place when calces of mercury, tin, and lead, are heated with charcoal powder. Hence the inference was obvious that carbonic acid is a compound of charcoal and oxygen, and therefore that all calces are compounds of their respective metals and oxygen.
Thus, although Lavoisier was unable to account for the phenomena connected with the evolution and absorption of hydrogen gas, he had conclusive evidence that the orthodox explanation was not the true one. He wisely, therefore, left it to time to throw light upon those parts of the theory that were still obscure.
His next paper, which was likewise inserted in the Memoirs of the Academy, for 1777, had some tendency to throw light on this subject, or at least it elucidated the constitution of sulphuric acid, which bore directly upon the antiphlogistic theory. It was entitled, "On the Solution of Mercury in vitriolic Acid, and on the Resolution of that Acid into aeriform sulphurous Acid, and into Air eminently Respirable."
He had already proved that sulphuric acid is a compound of sulphur and oxygen; and had even shown how the oxygen which the acid contained might be again separated from it, and exhibited in a separate state. Dr. Priestley had by this time made known the method of procuring sulphurous acid gas, by heating a mixture of mercury and sulphuric acid in a phial. This was the process which Lavoisier analyzed in the present paper. He put into a retort a mixture of four ounces mercury and six ounces concentrated sulphuric acid. The beak of the retort was plunged into a mercurial cistern, to collect the sulphurous acid gas as it was evolved; and heat being applied to the belly of the retort, sulphurous acid gas passed over in abundance, and sulphate of mercury was formed. The process was continued till the whole liquid contents of the retort had disappeared: then a strong heat was applied to the salt. In the first place, a quantity of sulphurous acid gas passed over, and lastly a portion of oxygen gas. The quicksilver was reduced to the metallic state. Thus he resolved sulphuric acid into sulphurous acid and oxygen. Hence it followed as a consequence, that sulphurous acid differs from sulphuric merely by containing a smaller quantity of oxygen.
The object of his next paper, published at the same time, was to throw light upon the pyrophorus of Homberg, which was made by kneading alum into a cake, with flour, or some substance containing abundance of carbon, and then exposing the mixture to a strong heat in close vessels, till it ceased to give out smoke. It was known that a pyrophorus thus formed takes fire of its own accord, and burns when it comes in contact with common air. It will not be necessary to enter into a minute analysis of this paper, because, though the experiments were very carefully made, yet it was impossible, at the time when the paper was drawn, to elucidate the phenomena of this pyrophorus in a satisfactory manner. There can be little doubt that the pyrophorus owes its property of catching fire, when in contact with air or oxygen, to a little potassium, which has been reduced to the metallic state by the action of the charcoal and sulphur on the potash in the alum. This substance taking fire, heat enough is produced to set fire to the carbon and sulphur which the pyrophorus contains. Lavoisier ascertained that during its combustion a good deal of carbonic acid was generated.
There appeared likewise another paper by Lavoisier, in the same volume of the academy, which may be mentioned, as it served still further to demonstrate the truth of the antiphlogistic theory. It is entitled, "On the Vitriolization of Martial Pyrites." Iron pyrites is known to be a compound of iron and sulphur. Sometimes this mineral may be left exposed to the air without undergoing any alteration, while at other times it speedily splits, effloresces, swells, and is converted into sulphate of iron. There are two species of pyrites; the one composed of two atoms of sulphur and one atom of iron, the other of one atom of sulphur and one atom of iron. The first of these is called bisulphuret of iron; the second protosulphuret, or simply sulphuret of iron. The variety of pyrites which undergoes spontaneous decomposition in the air, is known to be a compound, or rather mixture of the two species of pyrites.
Lavoisier put a quantity of the decomposing pyrites under a glass jar, and found that the process went on just as well as in the open air. He found that the air was deprived of the whole of its oxygen by the process, and that nothing was left but azotic gas. Hence the nature of the change became evident. The sulphur, by uniting with oxygen, was converted into sulphuric acid, while the iron became oxide of iron, and both uniting, formed sulphate of iron. There are still some difficulties connected with this change that require to be elucidated.
We have still another paper by Lavoisier, bearing on the antiphlogistic theory, published in the same volume of the Memoirs of the Academy, for 1778, entitled, "On Combustion in general." He establishes that the only air capable of supporting combustion is oxygen gas: that during the burning of bodies in common air, a portion of the oxygen of the atmosphere disappears, and unites with the burning body, and that the new compound formed is either an acid or a metallic calx. When sulphur is burnt, sulphuric acid is formed; when phosphorus, phosphoric acid; and when charcoal, carbonic acid. The calcination of metals is a process analogous to combustion, differing chiefly by the slowness of the process: indeed when it takes place rapidly, actual combustion is produced. After establishing these general principles, which are deduced from his preceding papers, he proceeds to examine the Stahlian theory of phlogiston, and shows that no evidence of the existence of any such principle can be adduced, and that the phenomena can all be explained without having recourse to it. Powerful as these arguments were, they produced no immediate effects. Nobody chose to give up the phlogistic theory to which he had been so long accustomed.
The next two papers of Lavoisier require merely to be mentioned, as they do not bear immediately upon the antiphlogistic theory. They appeared in the Memoirs of the Academy, for 1780. These memoirs were,
1. Second Memoir on the different Combinations of Phosphoric Acid.
2. On a particular Process, by means of which Phosphorus may be converted into phosphoric Acid, without Combustion.
The process here described consisted in throwing phosphorus, by a few grains at a time, into warm nitric acid of the specific gravity 1·29895. It falls to the bottom like melted wax, and dissolves pretty rapidly with effervescence: then another portion is thrown in, and the process is continued till as much phosphorus has been employed as is wanted; then the phosphoric acid may be obtained pure by distilling off the remaining nitric acid with which it is still mixed.
Hitherto Lavoisier had been unable to explain the anomalies respecting hydrogen gas, or to answer the objections urged against his theory in consequence of these anomalies. He had made several attempts to discover what peculiar substance was formed during the combustion of hydrogen, but always without success: at last, in 1783, he resolved to make the experiment upon so large a scale, that whatever the product might be, it should not escape him; but Sir Charles Blagden, who had just gone to Paris, informed him that the experiment for which he was preparing had already been made by Mr. Cavendish, who had ascertained that the product of the combustion of hydrogen was water. Lavoisier saw at a glance the vast importance of this discovery for the establishment of the antiphlogistic theory, and with what ease it would enable him to answer all the plausible objections which had been brought forward against his opinions in consequence of the evolution of hydrogen, when metals were calcined by solution in acids, and the absorption of it when metals were reduced in an atmosphere of this gas. He therefore resolved to repeat the experiment of Cavendish with every possible care, and upon a scale sufficiently large to prevent ambiguity. The experiment was made on the 24th of June, 1783, by Lavoisier and Laplace, in the presence of M. Le Roi, M. Vandermonde, and Sir Charles Blagden, who was at that time secretary of the Royal Society. The quantity of water formed was considerable, and they found that water was a compound of
1 volume oxygen
1·91 volume hydrogen.
Not satisfied with this, he soon after made another experiment along with M. Meusnier to decompose water. For this purpose a porcelain tube, filled with iron wire, was heated red-hot by being passed through a furnace, and then the steam of water was made to traverse the red-hot wire. To the further extremity of the porcelain tube a glass tube was luted, which terminated in a water-trough under an inverted glass receiver placed to collect the gas. The steam was decomposed by the red-hot iron wire, its oxygen united to the wire, while the hydrogen passed on and was collected in the water-cistern.
Both of these experiments, though not made till 1783, and though the latter of them was not read to the academy till 1784, were published in the volume of the Memoirs for 1781.
It is easy to see how this important discovery enabled Lavoisier to obviate all the objections to his theory from hydrogen. He showed that it was evolved when zinc or iron was dissolved in dilute sulphuric acid, because the water underwent decomposition, its oxygen uniting to the zinc or iron, and converting it into an oxide, while its hydrogen made its escape in the state of gas. Oxide of iron was reduced when heated in contact with hydrogen gas, because the hydrogen united to the oxygen of the acid and formed water, and of course the iron was reduced to the state of a metal. I consider it unnecessary to enter into a minute detail of these experiments, because, in fact, they added very little to what had been already established by Cavendish. But it was this discovery that contributed more than any thing else to establish the antiphlogistic theory. Accordingly, the great object of Dr. Priestley, and other advocates of the phlogistic theory, was to disprove the fact that water is a compound of oxygen and hydrogen. Scheele admitted the fact that water is a compound of oxygen and hydrogen; and doubtless, had he lived, would have become a convert to the antiphlogistic theory, as Dr. Black actually did. In short, it was the discovery of the compound nature of water that gave the Lavoisierian theory the superiority over that of Stahl. Till the time of this discovery every body opposed the doctrine of Lavoisier; but within a very few years after it, hardly any supporters of phlogiston remained. Nothing could be more fortunate for Lavoisier than this discovery, or afford him greater reason for self-congratulation.
We see the effect of this discovery upon his next paper, "On the Formation of Carbonic Acid," which appeared in the Memoirs of the Academy, for 1781. There, for the first time, he introduces new terms, showing, by that, that he considered his opinions as fully established. To the dephlogisticated air of Priestley, or his own pure air, he now gives the name of oxygen. The fixed air of Black he designates carbonic acid, because he considered it as a compound of carbon (the pure part of charcoal) and oxygen. The object of this paper is to determine the proportion of the constituents. He details a great many experiments, and deduces from them all, that carbonic acid gas is a compound of
| Carbon | 0·75 |
| Oxygen | 1·93 |
Now this is a tolerably near approximation to the truth. The true constituents, as determined by modern chemists, being
| Carbon | 0·75 |
| Oxygen | 2·00 |
The next paper of M. Lavoisier, which appeared in the Memoirs of the Academy, for 1782 (published in 1785), shows how well he appreciated the importance of the discovery of the composition of water. It is entitled, "General Considerations on the Solution of the Metals in Acids." He shows that when metals are dissolved in acids, they are converted into oxides, and that the acid does not combine with the metal, but only with its oxide. When nitric acid is the solvent the oxidizement takes place at the expense of the acid, which is resolved into nitrous gas and oxygen. The nitrous gas makes its escape, and may be collected; but the oxygen unites with the metal and renders it an oxide. He shows this with respect to the solution of mercury in nitric acid. He collected the nitrous gas given out during the solution of the metal in the acid: then evaporated the solution to dryness, and urged the fire till the mercury was converted into red oxide. The fire being still further urged, the red oxide was reduced, and the oxygen gas given off was collected and measured. He showed that the nitrous gas and the oxygen gas thus obtained, added together, formed just the quantity of nitric acid which had disappeared during the process. A similar experiment was made by dissolving iron in nitric acid, and then urging the fire till the iron was freed from every foreign body, and obtained in the state of black oxide.
It is well known that many metals held in solution by acids may be precipitated in the metallic state, by inserting into the solution a plate of some other metal. A portion of that new metal dissolves, and takes the place of the metal originally in solution. Suppose, for example, that we have a neutral solution of copper in sulphuric acid, if we put into the solution a plate of iron, the copper is thrown down in the metallic state, while a certain portion of the iron enters into the solution, combining with the acid instead of the copper. But the copper, while in solution, was in the state of an oxide, and it is precipitated in the metallic state. The iron was in the metallic state; but it enters into the solution in the state of an oxide. It is clear from this that the oxygen, during these precipitations, shifts its place, leaving the copper, and entering into combination with the iron. If, therefore, in such a case we determine the exact quantity of copper thrown down, and the exact quantity of iron dissolved at the same time, it is clear that we shall have the relative weight of each combined with the same weight of oxygen. If, for example, 4 of copper be thrown down by the solution of 3·5 of iron; then it is clear that 3·5 of iron requires just as much oxygen as 4 of copper, to turn both into the oxide that exists in the solution, which is the black oxide of each.
Bergman had made a set of experiments to determine the proportional quantities of phlogiston contained in the different metals, by the relative quantity of each necessary to precipitate a given weight of another from its acid solution. It was the opinion at that time, that metals were compounds of their respective calces and phlogiston. When a metal dissolved in an acid, it was known to be in the state of calx, and therefore had parted with its phlogiston: when another metal was put into this solution it became a calx, and the dissolved metal was precipitated in the metallic state. It had therefore united with the phlogiston of the precipitating metal. It is obvious, that by determining the quantities of the two metals precipitated and dissolved, the relative proportion of phlogiston in each could be determined. Lavoisier saw that these experiments of Bergman would serve equally to determine the relative quantity of oxygen in the different oxides. Accordingly, in a paper inserted in the Memoirs of the Academy, for 1782, he enters into an elaborate examination of Bergman's experiments, with a view to determine this point. But it is unnecessary to state the deductions which he drew, because Bergman's experiments were not sufficiently accurate for the object in view. Indeed, as the mutual precipitation of the metals is a galvanic phenomenon, and as the precipitated metal is seldom quite pure, but an alloy of the precipitating and precipitated metal; and as it is very difficult to dry the more oxidizable metals, as copper and tin, without their absorbing oxygen when they are in a state of very minute division; this mode of experimenting is not precise enough for the object which Lavoisier had in view. Accordingly the table of the composition of the metallic oxides which Lavoisier has drawn up is so very defective, that it is not worth while to transcribe it.
The same remark applies to the table of the affinities of oxygen which Lavoisier drew up and inserted in the Memoirs of the Academy, for the same year. His data were too imperfect, and his knowledge too limited, to put it in his power to draw up any such table with any approach to accuracy. I shall have occasion to resume the subject in a subsequent chapter.
In the same volume of the Memoirs of the Academy, this indefatigable man inserted a paper in order to determine the quantity of oxygen which combines with iron. His method of proceeding was, to burn a given weight of iron in oxygen gas. It is well known that iron wire, under such circumstances, burns with considerable splendour, and that the oxide, by the heat, is fused into a black brittle matter, having somewhat of the metallic lustre. He burnt 145·6 grains of iron in this way, and found that, after combustion, the weight became 192 grains, and 97 French cubic inches of oxygen gas had been absorbed. From this experiment it follows, that the oxide of iron formed by burning iron in oxygen gas is a compound of
| Iron | 3·5 |
| Oxygen | 1·11 |
This forms a tolerable approximation to the truth. It is now known, that the quantity of oxygen in the oxide of iron formed by the combustion of iron in oxygen gas is not quite uniform in its composition; sometimes it is a compound of
| Iron | 3½ |
| Oxygen | 1⅓ |
While at other times it consists very nearly of
| Iron | 3·5 |
| Oxygen | 1 |
and probably it may exist in all the intermediate proportions between these two extremes. The last of these compounds constitutes what is now known by the name of protoxide, or black oxide of iron. The first is the composition of the ore of iron so abundant, which is distinguished by the name of magnetic iron ore.
Lavoisier was aware that iron combines with more oxygen than exists in the protoxide; indeed, his analysis of peroxide of iron forms a tolerable approximation to the truth; but there is no reason for believing that he was aware that iron is capable of forming only two oxides, and that all intermediate degrees of oxidation are impossible. This was first demonstrated by Proust.
I think it unnecessary to enter into any details respecting two papers of Lavoisier, that made their appearance in the Memoirs of the Academy, for 1783, as they add very little to what he had already done. The first of these describes the experiments which he made to determine the quantity of oxygen which unites with sulphur and phosphorus when they are burnt: it contains no fact which he had not stated in his former papers, unless we are to consider his remark, that the heat given out during the burning of these bodies has no sensible weight, as new.
The other paper is "On Phlogiston;" it is very elaborate, but contains nothing which had not been already advanced in his preceding memoirs. Chemists were so wedded to the phlogistic theory, their prejudices were so strong, and their understandings so fortified against every thing that was likely to change their opinions, that Lavoisier found it necessary to lay the same facts before them again and again, and to place them in every point of view. In this paper he gives a statement of his own theory of combustion, which he had previously done in several preceding papers. He examines the phlogistic theory of Stahl at great length, and refutes it.
In the Memoirs of the Academy, for 1784, Lavoisier published a very elaborate set of experiments on the combustion of alcohol, oil, and different combustible bodies, which gave a beginning to the analysis of vegetable substances, and served as a foundation upon which this most difficult part of chemistry might be reared. He showed that during the combustion of alcohol the oxygen of the air united to the vapour of the alcohol, which underwent decomposition, and was converted into water and carbonic acid. From these experiments he deduced as a consequence, that the constituents of alcohol are carbon, hydrogen, and oxygen, and nothing else; and he endeavoured from his experiments to determine the relative proportions of these different constituents. From these experiments he concluded, that the alcohol which he used in his experiments was a compound of
| Carbon | 2629·5 part. |
| Hydrogen | 725·5 |
| Water | 5861 |
It would serve no purpose to attempt to draw any consequences from these experiments; as Lavoisier does not mention the specific gravity of the alcohol, of course we cannot say how much of the water found was merely united with the alcohol, and how much entered into its composition. The proportion between the carbon and hydrogen, constitutes an approximation to the truth, though not a very near one.
Olive oil he showed to be a compound of hydrogen and carbon, and bees' wax to be a compound of the same constituents, though in a different proportion.
This subject was continued, and his views further extended, in a paper inserted in the Memoirs of the Academy, for 1786, entitled, "Reflections on the Decomposition of Water by Vegetable and Animal Substances." He begins by stating that when charcoal is exposed to a strong heat, it gives out a little carbonic acid gas and a little inflammable air, and after this nothing more can be driven off, however high the temperature be to which it is exposed; but if the charcoal be left for some time in contact with the atmosphere it will again give out a little carbonic acid gas and inflammable gas when heated, and this process may be repeated till the whole charcoal disappears. This is owing to the presence of a little moisture which the charcoal imbibes from the air. The water is decomposed when the charcoal is heated and converted into carbonic acid and inflammable gas. When vegetable substances are heated in a retort, the water which they contain undergoes a similar decomposition, the carbon which forms one of their constituents combines with the oxygen and produces carbonic acid, while the hydrogen, the other constituent of the water, flies off in the state of gas combined with a certain quantity of carbon. Hence the substances obtained when vegetable or animal substances are distilled did not exist ready formed in the body operated on; but proceeded from the double decompositions which took place by the mutual action of the constituents of the water, sugar, mucus, &c., which the vegetable body contains. The oil, the acid, &c., extracted by distilling vegetable bodies did not exist in them, but are formed during the mutual action of the constituents upon each other, promoted as their action is by the heat. These views were quite new and perfectly just, and threw a new light on the nature of vegetable substances and on the products obtained by distilling them. It showed the futility of all the pretended analyses of vegetable substances, which chemists had performed by simply subjecting them to distillation, and the error of drawing any conclusions respecting the constituents of vegetable substances from the results of their distillation, except indeed with respect to their elementary constituents. Thus when by distilling a vegetable substance we obtain water, oil, acetic acid, carbonic acid, and carburetted hydrogen, we must not conclude that these principles existed in the substance, but merely that it contained carbon, hydrogen, and oxygen, in such proportions as to yield all these principles by decompositions.
As nitric acid acts upon metals in a very different way from sulphuric and muriatic acids, and as it is a much better solvent of metals in general than any other, it was an object of great importance towards completing the antiphlogistic theory to obtain an accurate knowledge of its constituents. Though Lavoisier did not succeed in this, yet he made at least a certain progress, which enabled him to explain the phenomena, at that time known, with considerable clearness, and to answer all the objections to the antiphlogistic theory from the action of nitric acid on metals. His first paper on the subject was published in the Memoirs of the Academy, for 1776. He put a quantity of nitric acid and mercury into a retort with a long beak, which he plunged into the water-trough. An effervescence took place and gas passed over in abundance, and was collected in a glass jar; the mercury being dissolved the retort was still further heated, till every thing liquid passed over into the receiver, and a dry yellow salt remained. The beak of the retort was now again plunged into the water-trough, and the salt heated till all the nitric acid which it contained was decomposed, and nothing remained in the retort but red oxide of mercury. During this last process much more gas was collected. All the gas obtained during the solution of the mercury and the decomposition of the salt was nitrous gas. The red oxide of mercury was now heated to redness, oxygen gas was emitted in abundance, and the mercury was reduced to the metallic state: its weight was found the very same as at first. It is clear, therefore, that the nitrous gas and the oxygen gas were derived, not from the mercury but from the nitric acid, and that the nitric acid had been decomposed into nitrous gas and oxygen: the nitrous gas had made its escape in the form of gas, and the oxygen had remained united to the metal.
From these experiments it follows clearly, that nitric acid is a compound of nitrous gas and oxygen. The nature of nitrous gas itself Lavoisier did not succeed in ascertaining. It passed with him for a simple substance; but what he did ascertain enabled him to explain the action of nitric acid on metals. When nitric acid is poured upon a metal which it is capable of dissolving, copper for example, or mercury, the oxygen of the acid unites to the metal, and converts into an oxide, while the nitrous gas, the other constituent of the acid, makes its escape in the gaseous form. The oxide combines with and is dissolved by another portion of the acid which escapes decomposition.
It was discovered by Dr. Priestley, that when nitrous gas and oxygen gas are mixed together in certain proportions, they instantly unite, and are converted into nitrous acid. If this mixture be made over water, the volume of the gases is instantly diminished, because the nitrous acid formed loses its elasticity, and is absorbed by the water. When nitrous gas is mixed with air containing oxygen gas, the diminution of volume after mixture is greater the more oxygen gas is present in the air. This induced Dr. Priestley to employ nitrous gas as a test of the purity of common air. He mixed together equal volumes of the nitrous gas and air to be examined, and he judged of the purity of the air by the degree of condensation: the greater the diminution of bulk, the greater did he consider the proportion of oxygen in the air under examination to be. This method of proceeding was immediately adopted by chemists and physicians; but there was a want of uniformity in the mode of proceeding, and a considerable diversity in the results. M. Lavoisier endeavoured to improve the process, in a paper inserted in the Memoirs of the Academy, for 1782; but his method did not answer the purpose intended: it was Mr. Cavendish that first pointed out an accurate mode of testing air by means of nitrous gas, and who showed that the proportions of oxygen and azotic gas in common air are invariable.
Lavoisier, in the course of his investigations, had proved that carbonic acid is a compound of carbon and oxygen; sulphuric acid, of sulphur and oxygen; phosphoric acid, of phosphorus and oxygen; and nitric acid, of nitrous gas and oxygen. Neither the carbon, the sulphur, the phosphorus, nor the nitrous gas, possessed any acid properties when uncombined; but they acquired these properties when they were united to oxygen. He observed further, that all the acids known in his time which had been decomposed were found to contain oxygen, and when they were deprived of oxygen, they lost their acid properties. These facts led him to conclude, that oxygen is an essential constituent in all acids, and that it is the principle which bestows acidity or the true acidifying principle. This was the reason why he distinguished it by the name of oxygen.[5] These views were fully developed by Lavoisier, in a paper inserted in the Memoirs of the Academy, for 1778, entitled, "General Considerations on the Nature of Acids, and on the Principles of which they are composed." When this paper was published, Lavoisier's views were exceedingly plausible. They were gradually adopted by chemists in general, and for a number of years may be considered to have constituted a part of the generally-received doctrines. But the discovery of the nature of chlorine, and the subsequent facts brought to light respecting iodine, bromine, and cyanogen, have demonstrated that it is inaccurate; that many powerful acids exist which contain no oxygen, and that there is no one substance to which the name of acidifying principle can with justice be given. To this subject we shall again revert, when we come to treat of the more modern discoveries. , sour, and γινομαι, which he defined the producer of acids, the acidifying principle.]
Long as the account is which we have given of the labours of Lavoisier, the subject is not yet exhausted. Two other papers of his remain to be noticed, which throw considerable light on some important functions of the living body: we allude to his experiments on respiration and perspiration.
It was known, that if an animal was confined beyond a certain limited time in a given volume of atmospherical air, it died of suffocation, in consequence of the air becoming unfit for breathing; and that if another animal was put into this air, thus rendered noxious by breathing, its life was destroyed almost in an instant. Dr. Priestley had thrown some light upon this subject by showing that air, in which an animal had breathed for some time, possessed the property of rendering lime-water turbid, and therefore contained carbonic acid gas. He considered the process of breathing as exactly analogous to the calcination of metals, or the combustion of burning bodies. Both, in his opinion acted by giving out phlogiston; which, uniting with the air of the atmosphere, converted it into phlogisticated air. Priestley found, that if plants were made to vegetate for some time in air that had been rendered unfit for supporting animal life by respiration, it lost the property of extinguishing a candle, and animals could breathe it again without injury. He concluded from this that animals, by breathing, phlogisticated air, but that plants, by vegetating, dephlogisticated air: the former communicated phlogiston to it, the latter took phlogiston from it.
After Lavoisier had satisfied himself that air is a mixture of oxygen and azote, and that oxygen alone is concerned in the processes of calcination and combustion, being absorbed and combined with the substances undergoing calcination and combustion, it was impossible for him to avoid drawing similar conclusions with respect to the breathing of animals. Accordingly, he made experiments on the subject, and the result was published in the Memoirs of the Academy, for 1777. From these experiments he drew the following conclusions:
1. The only portion of atmospherical air which is useful in breathing is the oxygen. The azote is drawn into the lungs along with the oxygen, but it is thrown out again unaltered.
2. The oxygen gas, on the contrary, is gradually, by breathing, converted into carbonic acid; and air becomes unfit for respiration when a certain portion of its oxygen is converted into carbonic acid gas.
3. Respiration is therefore exactly analogous to calcination. When air is rendered unfit for supporting life by respiration, if the carbonic acid gas formed be withdrawn by means of lime-water, or caustic alkali, the azote remaining is precisely the same, in its nature, as what remains after air is exhausted of its oxygen by being employed for calcining metals.
In this first paper Lavoisier went no further than establishing these general principles; but he afterwards made experiments to determine the exact amount of the changes which were produced in air by breathing, and endeavoured to establish an accurate theory of respiration. To this subject we shall have occasion to revert again, when we give an account of the attempts made to determine the phenomena of respiration by more modern experimenters.
Lavoisier's experiments on perspiration were made during the frenzy of the French revolution, when Robespierre had usurped the supreme power, and when it was the object of those at the head of affairs to destroy all the marks of civilization and science which remained in the country. His experiments were scarcely completed when he was thrown into prison, and though he requested a prolongation of his life for a short time, till he could have the means of drawing up a statement of their results, the request was barbarously refused. He has therefore left no account of them whatever behind him. But Seguin, who was associated with him in making these experiments, was fortunately overlooked, and escaped the dreadful times of the reign of terror: he afterwards drew up an account of the results, which has prevented them from being wholly lost to chemists and physiologists.