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chemistry

  (kĕm'ĭ-strē) pronunciation
n., pl. -tries.
  1. The science of the composition, structure, properties, and reactions of matter, especially of atomic and molecular systems.
  2. The composition, structure, properties, and reactions of a substance.
  3. The elements of a complex entity and their dynamic interrelation: “Now that they had a leader, a restless chemistry possessed the group” (John Updike).
  4. Mutual attraction or sympathy; rapport: The chemistry was good between the partners.

 
 

Chemistry is the study of the chemical and physical change of matter.

Early U.S. Chemistry and Chemical Societies

The beginning of chemistry in the United States came in the form of manufacturing goods such as glass, ink, and gunpowder. In the mid-1700s, some academic instruction in chemistry started in Philadelphia. The earliest known academic institution to formally teach chemistry was the medical school of the College of Philadelphia, where Benjamin Rush was appointed the chair of chemistry in 1769. Not only was Rush the first American chemistry teacher, he may have been the first to publish a chemistry textbook written in the United States. In 1813, the Chemical Society of Philadelphia published the first American chemical journal, Transactions. Although other chemical societies existed at that time, the Philadelphia Chemical Society was the first society to publish its own journal. Unfortunately, the journal and chemical society lasted only one year.

Sixty years later, in 1874, at Joseph Priestley's home in Northumberland, Pennsylvania, a number of renowned scientists gathered to celebrate Priestley's 1774 discovery of oxygen. It was at this gathering that Charles F. Chandler proposed the concept of an American chemical society. The proposal was turned down, in part because the American Association for the Advancement of Science (AAAS) had a chemical section that provided an adequate forum for assembly and debate. Two years later, a national society, based in New York and called the American Chemical Society, was formed with John W. Draper as its first president. Since New York chemists dominated most of the meetings and council representative positions, the Washington Chemical Society was founded in 1884 by two chemists based in Washington, D.C., Frank W. Clarke and Harvey W. Wiley. In 1890, the American Chemical Society constitution was changed to encourage the formation of local sections, such as New York, Washington, and other chemical societies in the United States, thereby leading to a national organization. By 1908, the society had approximately 3,400 members, outnumbering the German Chemical Society, which at that time was the center of world chemistry. Today, the American Chemical Society has some 163,503 members, and the United States is considered the center of world chemistry. In addition to its premier journal, the Journal of the American Chemical Society, the society also publishes several other journals that are divisional in nature, including the Journal of Organic Chemistry, Analytical Chemistry, Journal of Physical Chemistry, Inorganic Chemistry, and Biochemistry. The society also produces a publication called Chemical Abstracts, which catalogs abstracts from thousands of papers printed in chemical journals around the world.

European Influences

Although the various disciplines of chemistry—organic, inorganic, analytical, biochemistry, and physical chemistry—have a rich American history, they have also been influenced by European, especially German, chemists. The influence of physical chemistry on the development of chemistry in the United States began with American students who studied under a number of German chemists, most notably the 1909 Nobel Prize winner, Wilhelm Ostwald. In a 1946 survey by Stephen S. Visher, three of Ostwald's students were recognized as influential chemistry teachers—Gilbert N. Lewis, Arthur A. Noyes, and Theodore W. Richards. Of these three, Richards would be awarded the 1914 Nobel Prize for his contributions in accurately determining the atomic weight of a large number of chemical elements. Lewis and Noyes would go on to play a major role in the development of academic programs at institutions such as the University of California at Berkeley, the Massachusetts Institute of Technology, and Caltech. While at these institutions Lewis and Noyes attracted and trained numerous individuals, including William C. Bray, Richard C. Tolman, Joel H. Hildebrand, Merle Randall, Glenn T. Seaborg, and Linus Pauling. These individuals placed physical chemistry at the center of their academic programs and curricula. Students from these institutions, as well as other universities across America, took the knowledge they gained in physical chemistry to places like the Geophysical Laboratories, General Electric, Pittsburgh Plate Glass Company, and Bausch and Lomb.

Influence could also flow from America to Europe, as it did with one of the earliest great American chemists, J. Willard Gibbs (1839–1903). Gibbs, educated at Yale University, was the first doctor of engineering in the United States. His contribution to chemistry was in the field of thermodynamics—the study of heat and its transformations. Using thermodynamic principles, he deduced the Gibbs phase rule, which relates the number of components and phases of mixtures to the degrees of freedom in a closed system. Gibbs's work did not receive much attention in the United States due to its publication in a minor journal, but in Europe his ideas were well received by the physics community, including Wilhelm Ostwald, who translated Gibbs's work into German.

A second influence from Europe came around the 1920s, when a very bright student from Caltech named Linus Pauling went overseas as a postdoctoral fellow for eighteen months. In Europe, Pauling spent time working with Niels Bohr, Erwin Schrödinger, Arnold Sommerfeld, Walter Heitler, and Fritz London. During this time, Pauling trained himself in the new area of quantum mechanics and its application to chemical bonding. A significant part of our knowledge about the chemical bond and its properties is due to Pauling. Upon his return from Europe, Pauling went to back to Caltech and in 1950 published a paper explaining the nature of helical structures in proteins.

At the University of California at Berkeley, Gilbert N. Lewis directed a brilliant scientist, Glenn T. Seaborg. Seaborg worked as Lewis's assistant on acid-base chemistry during the day and at night he explored the mysteries of the atom. Seaborg is known for leading the first group to discover plutonium. This discovery would lead him to head a section on the top secret Manhattan Project, which created the first atomic bomb. Seaborg's second biggest achievement was his proposal to modify the periodic table to include the actinide series. This concept predicted that the fourteen actinides, including the first eleven transuranium elements, would form a transition series analogous to the rare-earth series of lanthanide elements and therefore show how the transuranium elements fit into the periodic table. Seaborg's work on the transuranium elements led to his sharing the 1951 Nobel Prize in chemistry with Edwin McMillan. In 1961, Seaborg became the chairman of the Atomic Energy Commission, where he remained for ten years.

Perhaps Seaborg's greatest contribution to chemistry in the United States was his advocacy of science and mathematics education. The cornerstone of his legacy on education is the Lawrence Hall of Science on the Berkeley campus, a public science center and institution for curriculum development and research in science and mathematics education. Seaborg also served as principal investigator of the well-known Great Explorations in Math and Science (GEMS) program, which publishes the many classes, workshops, teacher's guides, and handbooks from the Lawrence Hall of Science. To honor a brilliant career by such an outstanding individual, element 106 was named Seaborgium.

Twentieth-Century Research and Discoveries

Research in the American chemical industry started in the early twentieth century with the establishment of research laboratories such as General Electric, Eastman Kodak, AT&T, and DuPont. The research was necessary in order to replace badly needed products and chemicals that were normally obtained from Germany. Industry attracted re-search chemists from their academic labs and teaching assignments to head small, dynamic research groups. In 1909, Irving Langmuir was persuaded to leave his position as a chemistry teacher at Stevens Institute of Technology to do research at General Electric. It was not until World War I that industrial chemical research took off. Langmuir was awarded a Nobel Prize for his industrial work. In the early 1900s, chemists were working on polymer projects and free radical reactions in order to synthesize artificial rubber. DuPont hired Wallace H. Carothers, who worked on synthesizing polymers. A product of Carothers's efforts was the synthesis of nylon, which would become DuPont's greatest moneymaker. In 1951, modern organometallic chemistry began at Duquesne University in Pittsburgh with the publication of an article in the journal Nature on the synthesis of an organo-iron compound called dicyclopentadienyliron, better known as ferrocene. Professor Peter Pauson and Thomas J. Kealy, a student, were the first to publish its synthesis, and two papers would be published in 1952 with the correct predicted structure. One paper was by Robert Burns Woodward, Geoffrey Wilkinson, Myron Rosenblum, and Mark Whiting; the second was by Ernst Otto Fischer and Wolfgang Pfab. Finally, a complete crystal structure of ferrocene was published in separate papers by Phillip F. Eiland and Ray Pepinsky and by Jack D. Dunitz and Leslie E. Orgel. The X-ray crystallographic structures would confirm the earlier predicted structures. Ferrocene is a "sandwich" compound in which an iron ion is sandwiched between two cyclopentadienyl rings. The discovery of ferrocene was important in many aspects of chemistry, such as revisions in bonding concepts, synthesis of similar compounds, and uses of these compounds as new materials. Most importantly, the discovery of ferrocene has merged two distinct fields of chemistry, organic and inorganic, and led to important advances in the fields of homogeneous catalysis and polymerization.

Significant American achievements in chemistry were recognized by the Nobel Prize committee in the last part of the twentieth century and the first years of the twenty-first century. Some examples include: the 1993 award to Kary B. Mullis for his work on the polymerase chain reaction (PCR); the 1996 award to Robert F. Curl Jr. and Richard E. Smalley for their part in the discovery of C60, a form of molecular carbon; the 1998 award to John A. Pople and Walter Kohn for the development of computational methods in quantum chemistry; the 1999 award to Ahmed H. Zewail for his work on reactions using femtosecond (10-14 seconds) chemistry; the 2000 award to Alan G. MacDiarmid and Alan J. Heeger for the discovery and development of conductive polymers; and the 2001 award to William S. Knowles and K. Barry Sharpless for their work on asymmetric synthesis. The outcomes of these discoveries are leading science in the twenty-first century. The use of PCR analysis has contributed to the development of forensic science. The discovery C60 and related carbon compounds, known as nanotubes, is leading to ideas in drug delivery methods and the storage of hydrogen and carbon dioxide. The computational tools developed by Pople and Kohn are being used to assist scientists in analyzing and designing experiments. Femtosecond chemistry is providing insight into how bonds are made and broken as a chemical reaction proceeds. Heeger and MacDiarmid's work has led to what is now known as plastic electronics—devices made of conducting polymers, ranging from light-emitting diodes to flat panel displays. The work by Knowles and Sharpless has provided organic chemists with the tools to synthesize compounds that contain chirality or handedness. This has had a tremendous impact on the synthesis of drugs, agrochemicals, and petrochemicals.

Bibliography

Brock, William H. The Norton History of Chemistry. New York: Norton, 1993.

———. The Chemical Tree: A History of Chemistry. New York: Norton, 2000.

Greenberg, Arthur. A Chemical History Tour: Picturing Chemistry from Alchemy to Modern Molecular Science. New York: Wiley, 2000.

Servos, John W. Physical Chemistry from Ostwald to Pauling: The Making of Science in America. Princeton, N.J.: Princeton University Press, 1990.

—Jeffrey D. Madura

 
branch of science concerned with the properties, composition, and structure of substances and the changes they undergo when they combine or react under specified conditions.

Branches of Chemistry

Chemistry can be divided into branches according to either the substances studied or the types of study conducted. The primary division of the first type is between inorganic chemistry and organic chemistry. Divisions of the second type are physical chemistry and analytical chemistry.

The original distinction between organic and inorganic chemistry arose as chemists gradually realized that compounds of biological origin were quite different in their general properties from those of mineral origin; organic chemistry was defined as the study of substances produced by living organisms. However, when it was discovered in the 19th cent. that organic molecules can be produced artificially in the laboratory, this definition had to be abandoned. Organic chemistry is most simply defined as the study of the compounds of carbon. Inorganic chemistry is the study of chemical elements and their compounds (with the exception of carbon compounds).

Physical chemistry is concerned with the physical properties of materials, such as their electrical and magnetic behavior and their interaction with electromagnetic fields. Subcategories within physical chemistry are thermochemistry, electrochemistry, and chemical kinetics. Thermochemistry is the investigation of the changes in energy and entropy that occur during chemical reactions and phase transformations (see states of matter). Electrochemistry concerns the effects of electricity on chemical changes and interconversions of electric and chemical energy such as that in a voltaic cell. Chemical kinetics is concerned with the details of chemical reactions and of how equilibrium is reached between the products and reactants.

Analytical chemistry is a collection of techniques that allows exact laboratory determination of the composition of a given sample of material. In qualitative analysis all the atoms and molecules present are identified, with particular attention to trace elements. In quantitative analysis the exact weight of each constituent is obtained as well. Stoichiometry is the branch of chemistry concerned with the weights of the chemicals participating in chemical reactions. See also chemical analysis.

History of Chemistry

The earliest practical knowledge of chemistry was concerned with metallurgy, pottery, and dyes; these crafts were developed with considerable skill, but with no understanding of the principles involved, as early as 3500 B.C. in Egypt and Mesopotamia. The basic ideas of element and compound were first formulated by the Greek philosophers during the period from 500 to 300 B.C. Opinion varied, but it was generally believed that four elements (fire, air, water, and earth) combined to form all things. Aristotle's definition of a simple body as “one into which other bodies can be decomposed and which itself is not capable of being divided” is close to the modern definition of element.

About the beginning of the Christian era in Alexandria, the ancient Egyptian industrial arts and Greek philosophical speculations were fused into a new science. The beginnings of chemistry, or alchemy, as it was first known, are mingled with occultism and magic. Interests of the period were the transmutation of base metals into gold, the imitation of precious gems, and the search for the elixir of life, thought to grant immortality. Muslim conquests in the 7th cent. A.D. diffused the remains of Hellenistic civilization to the Arab world. The first chemical treatises to become well known in Europe were Latin translations of Arabic works, made in Spain c.A.D. 1100; hence it is often erroneously supposed that chemistry originated among the Arabs. Alchemy developed extensively during the Middle Ages, cultivated largely by itinerant scholars who wandered over Europe looking for patrons.

Evolution of Modern Chemistry

In the hands of the “Oxford Chemists” (Robert Boyle, Robert Hooke, and John Mayow) chemistry began to emerge as distinct from the pseudoscience of alchemy. Boyle (1627–91) is often called the founder of modern chemistry (an honor sometimes also given Antoine Lavoisier, 1743–94). He performed experiments under reduced pressure, using an air pump, and discovered that volume and pressure are inversely related in gases (see gas laws). Hooke gave the first rational explanation of combustion—as combination with air—while Mayow studied animal respiration. Even as the English chemists were moving toward the correct theory of combustion, two Germans, J. J. Becher and G. E. Stahl, introduced the false phlogiston theory of combustion, which held that the substance phlogiston is contained in all combustible bodies and escapes when the bodies burn.

The discovery of various gases and the analysis of air as a mixture of gases occurred during the phlogiston period. Carbon dioxide, first described by J. B. van Helmont and rediscovered by Joseph Black in 1754, was originally called fixed air. Hydrogen, discovered by Boyle and carefully studied by Henry Cavendish, was called inflammable air and was sometimes identified with phlogiston itself. Cavendish also showed that the explosion of hydrogen and oxygen produces water. C. W. Scheele found that air is composed of two fluids, only one of which supports combustion. He was the first to obtain pure oxygen (1771–73), although he did not recognize it as an element. Joseph Priestley independently discovered oxygen by heating the red oxide of mercury with a burning glass; he was the last great defender of the phlogiston theory.

The work of Priestley, Black, and Cavendish was radically reinterpreted by Lavoisier, who did for chemistry what Newton had done for physics a century before. He made no important new discoveries of his own; rather, he was a theoretician. He recognized the true nature of combustion, introduced a new chemical nomenclature, and wrote the first modern chemistry textbook. He erroneously believed that all acids contain oxygen.

Impact of the Atomic Theory

The assumption that compounds were of definite composition was implicit in 18th-century chemistry. J. L. Proust formally stated the law of constant proportions in 1797. C. L. Berthollet opposed this law, holding that composition depended on the method of preparation. The issue was resolved in favor of Proust by John Dalton's atomic theory (1808). The atomic theory goes back to the Greeks, but it did not prove fruitful in chemistry until Dalton ascribed relative weights to the atoms of chemical elements. Electrochemical theories of chemical combinations were developed by Humphry Davy and J. J. Berzelius. Davy discovered the alkali metals by passing an electric current through their molten oxides. Michael Faraday discovered that a definite quantity of charge must flow in order to deposit a given weight of material in solution. Amedeo Avogadro introduced the hypothesis that equal volumes of gases at the same pressure and temperature contain the same number of molecules.

William Prout suggested that as all elements seemed to have atomic weights that were multiples of the atomic weight of hydrogen, they could all be in some way different combinations of hydrogen atoms. This contributed to the concept of the periodic table of the elements, the culmination of a long effort to find regular, systematic properties among the elements. Periodic laws were put forward almost simultaneously and independently by J. L. Meyer in Germany and D. I. Mendeleev in Russia (1869). An early triumph of the new theory was the discovery of new elements that fit the empty spaces in the table. William Ramsay's discovery, in collaboration with Lord Rayleigh, of argon and other inert gases in the atmosphere extended the periodic table

Organic Chemistry and the Modern Era

Organic chemistry developed extensively in the 19th cent., prompted in part by Friedrich Wohler's synthesis of urea (1828), which disproved the belief that only living organisms could produce organic molecules. Other important organic chemists include Justus von Liebig, C. A. Wurtz, and J. B. Dumas. In 1852 Edward Frankland introduced the idea of valency (see valence), and in 1858 F. A. Kekule showed that carbon atoms are tetravalent and are linked together in chains. Kekule's ring structure for benzene opened the way to modern theories of organic chemistry. Henri Louis Le Châtelier, J. H. van't Hoff, and Wilhelm Ostwald pioneered the application of thermodynamics to chemistry. Further contributions were the phase rule of J. W. Gibbs, the ionization equilibrium theory of S. A. Arrhenius, and the heat theorem of Walther Nernst. Ernst Fischer's work on the amino acids marks the beginning of molecular biology.

At the end of the 19th cent., the discovery of the electron by J. J. Thomson and of radioactivity by A. E. Becquerel revealed the close connection between chemistry and physics. The work of Ernest Rutherford, H. G. J. Moseley, and Niels Bohr on atomic structure (see atom) was applied to molecular structures. G. N. Lewis, Irving Langmuir, and Linus Pauling developed the electronic theory of chemical bonds, directed valency, and molecular orbitals (see molecular orbital theory). Transmutation of the elements, first achieved by Rutherford, has led to the creation of elements not found in nature; in work pioneered by Glenn Seaborg elements heavier than uranium have been produced. With the rapid development of polymer chemistry after World War II a host of new synthetic fibers and materials have been added to the market. A fuller understanding of the relation between the structure of molecules and their properties has allowed chemists to tailor predictively new materials to meet specific needs.

Bibliography

See I. Asimov, A Short History of Chemistry (1965); D. A. McQuarrie and P. A. Rock, General Chemistry (1984); L. Pauling, General Chemistry (3d ed. 1991); R. C. Weast, ed., CRC Handbook of Chemistry and Physics (published annually).


 
History 1450-1789: Chemistry

The history of early modern chemistry, understood as a body of ideas and practices related to compounding and decomposing material substances, takes us to alchemy and apothecary laboratories, artisans' workshops, metallurgists and manufacturers, scientific societies, arsenals, royal courts, and public squares. It should not be understood in terms of the victory of scientific theory over arcane beliefs, but of the changing employment of its various technologies and the contexts in and by which they were legitimized.

Material and Bodily Technology

Chemistry's material technology—that is, its instruments and laboratory equipment—remained stable throughout most of the period, but was augmented by precision-oriented apparatus in the second half of the eighteenth century as the study of heat and gases, along with early industrial innovations, redirected chemical investigations. Increasingly accurate measuring devices helped bring about standardization in manufacturing ventures (e.g. Josiah Wedgwood's pottery works) while feeding debates over how to organize chemistry as an investigative enterprise. Should the heterogeneous chemical world be disciplined by analyzing qualitative or quantitative data?

The way chemical operators and investigators used their own bodies was part of this historical development and debate. As long as chemical determination rested on examining colors, smells, tastes and textures, the human senses served as crucial chemical instruments. As experimental claims increasingly relied on precise measurements by the late eighteenth century (a hallmark of the chemical revolution), sense evidence became "subjective" and, hence, a questionable foundation for proof. Chemists continued to rely on their senses, but proof became increasingly a matter of quantitative determination.

Theory and Practice

The question of what constituted a primary chemical element was not a part of practical chemists' daily routine. Neither, prior to the late eighteenth century, was there a direct correlation between one's theoretical views and how one actually carried out chemical procedures, which can be seen by examining the impact of the mechanical philosophy on chemistry. Textbook writers such as Nicolas Lémery (1645–1715) attributed a substance's qualities to the shape of particles that composed it. But authors left such explanations behind when dealing with actual chemical operations. Robert Boyle (1627–1691), often labeled a mechanical philosopher, made a bigger impact on chemistry through his interests in practical knowledge and alchemy. Even Isaac Newton's (1642–1727) mechanism, which married particles to short-range forces, hardly touched chemical practice—although theorists such as Georges-Louis Leclerc de Buffon (1707–1788) hoped chemical attraction (affinities) could be explained mathematically with Newtonian forces. Working chemists continued to learn their trade through apprenticeship and to be guided by practical recipes. Acquiring tacit knowledge and practical skills, then, were certainly as important for the historical development of chemistry as theoretical knowledge.

It is, however, historically important that matter theory became linked to chemical research in an increasingly instrumental way by the eighteenth century. Paracelsus (1493–1541), who argued for the chemical foundation of medicine (iatrochemistry), claimed that Aristotle's four elements appeared in bodies as mercury, sulfur, and salt. Mercury was the principle of volatility and fusibility, sulfur of inflammability, and salt of incombustibility. Therefore, chemists might recognize a compound not only as heavy or wet, but also as liable to specific chemical processes.

Johann Joachim Becher (1635–1682) substituted three categories of earth for Paracelsus's principles and explained material change largely in terms of their combination with and release from compounds through processes such as combustion. His student George Ernst Stahl (1660–1734) further codified Becher's work, giving the name "phlogiston" (from the Greek verb "to inflame") to Becher's terra pinguis (the sulfur of inflammability) and teaching that phlogiston's presence was responsible for characteristics including metallicity, color, and inflammability. In France, the influential chemistry lecturer Guillaume François Rouelle (1703–1770) popularized the idea of phlogiston, associating it with fire. Others such as Joseph Priestley (1733–1804) identified it variously with electricity and hydrogen. Phlogiston was used to explain phenomena including combustion, calcination, and the quality of air, thereby organizing a number of research activities under a set of interconnecting theories and emphasizing the potential reversibility of chemical processes.

Others began considering the Aristotelian elements as material instruments. Stephen Hales (1677–1761) focused on the expansion of air and the way in which it could become "fixed" in bodies. Herman Boerhaave (1668–1738) went further, organizing his chemistry lectures largely around the investigative consequences of considering earth, water, air, and fire as instruments that afforded specific chemical processes. A Newtonian by public pronouncement, Boerhaave actually did much more to stimulate chemical research by focusing on the reactive effects of these elemental instruments. He related fire (the substance of heat) to the primary processes of expansion and repulsion. He presented air and water as providing containers in which other particles were suspended. It wasn't long before these "instruments" themselves were subjected to chemical analysis, as investigators sought to understand whether their "instrumental" presence was chemically passive or active. Research in the second half of the eighteenth century was marked by investigations of newly discovered gases (qualitatively distinct "airs"), the role of heat, and, in the 1780s, the composition of water.

Literary Technology

Chemical theory and instrumental research practices were also linked in the way chemical knowledge came to be organized nomenclaturally and in analytical tables (chemistry's literary technology). Related to the heritage of alchemy and the various contexts in which chemical substances were discovered and used, chemical nomenclature was traditionally a colorfully unsystematic affair. Growing interest in chemical research in the second half of the eighteenth century, especially the investigation of a number of new "airs," led chemists to consider nomenclatural reform. Standard conventions for naming new substances would allow researchers from various communities to communicate. In 1787 Antoine Laurent Lavoisier (1743–1794), Louis Bernard Guyton de Morveau (1737–1816), Antoine François Fourcroy (1755–1809), and Claude Simon Berthollet (1748–1822) revamped chemistry's nomenclature totally, enunciating in their Méthode de nomenclature chimique a revolutionary way to structure chemistry's investigative knowledge and practices.

Oxygen's discovery and naming provides a good example. Recognized in the 1770s as a distinct "air" responsible for combustion, supporting respiration, and the process of calcination, it was variously named the "purest part of air," "fire air," "eminently respirable air," and "dephlogisticated air." Lavoisier focused on what he considered its most far-reaching characteristic and argued that it should be called "oxygen," the "generator" of acids. Not only did he use oxygen's causal properties to argue against the existence of phlogiston, he named the substance in a way that simultaneously reflected how the relation between these properties ought to be understood and how chemists ought to pursue future research.

Traditionally, the secretive nature of many alchemical and artisanal practices had combined with chemistry's lack of institutional and disciplinary unity to work against the development of a public, systematic means of recording compositional data. This began changing when Étienne François Geoffroy (1672–1731) presented his "Table of the different relationships observed between different substances" to the French Academy of Sciences in 1718. Recording and publishing these relationships, often called affinities, provided a handy way for chemists to share and expand empirical knowledge without having to agree on their theoretical explanation. As the century progressed, affinity and solvent tables became more sophisticated (recording, for example, how relations were observed), leading chemists to hope that their field might thereby gain the certainty of a scientific discipline. As was true with nomenclatural reform, this was largely achieved by Lavoisier and his colleagues, with revolutionary results. Lavoisier's 1789 textbook Traitéélémentaire de chimie included tables whose structures redirected research along the same lines as chemistry's new nomenclature.

Lavoisier began his textbook by arguing that humans live in a Condillacian world; chemists should therefore build their discipline on a foundation of sensible facts. Chemistry's nomenclature should express only what chemists actively observed; its basic elements should be defined by laboratory procedures. In fact, Lavoisier began his "table of simple substances" with five elements that could never be isolated, but which he made responsible for fundamental chemical processes. Oxygen "generates" acidity, hydrogen "generates" water. Caloric, the substance of heat, interacts with chemical affinities to regulate composition and decomposition. In place of affinity and solvent tables, Lavoisier filled his textbook with tables that simultaneously recorded and predicted the combinatorial powers of elements such as oxygen. Together they formed an integrated research program intended to discipline chemistry.

Chemistry's Instrumentalization

Lavoisier's laboratory practices reflected what appeared on the pages of his book, the last third of which treated laboratory instruments. If primary elements couldn't be isolated, Lavoisier argued that their active presence could be quantitatively traced. Unmeasurable phlogiston was out, precision balances were in, as seen in his proof that water is compounded of hydrogen and oxygen. Affinities could not yet be quantified, but the effect of caloric on composition and decomposition could be quantitatively inferred by the melting of ice in an ice calorimeter—an instrument designed by Lavoisier. In general, nomenclature, instrumental theory, and measurement provided a research program for future chemists, in terms of both questions and methods for resolving them.

This culmination of chemistry's instrumentalization was, arguably, the essence of the chemical revolution. Whether others adopted Lavoisier's theories or followed the specifics of his research proposals, the modern discipline of chemistry was permanently marked by the instrumental bounds he prescibed.

Bibliography

Bensaude-Vincent, Bernadette. Lavoisier. Memoires d'une révolution. Paris, 1993.

Golinski, Jan. Science as Public Culture: Chemistry and Enlightenment in Britain 1760–1820. Cambridge, U.K., 1992.

Hannaway, Owen. The Chemist and the Word: The Didactic Origins of Chemistry. Baltimore, 1985.

Holmes, Frederick Lawrence. Eighteenth-Century Chemistry as an Investigative Enterprise. Berkeley, 1989.

Roberts, Lissa. "The Death of the Sensuous Chemist: the 'New' Chemistry and the Transformation of Sensuous Technology." Studies in History and Philosophy of Science 26 (1995): 503–529.

——. "Setting the Table: The Disciplinary Development of Eighteenth-Century Chemistry as Read through the Changing Structure of its Tables." In The Literary Structure of Scientific Argument, edited by Peter Dear, pp. 99–132. Philadelphia, 1991.

—LISSA ROBERTS

 
Quotes About: Chemistry

Quotes:

"I feel like a white granular mass of amorphous crystals -- my formula appears to be isomeric with Spasmotoxin. My aurochloride precipitates into beautiful prismatic needles. My Platinochloride develops octahedron crystals, -- with a fine blue florescence. My physiological action is not indifferent. One millionth of a grain injected under the skin of a frog produced instantaneous death accompanied by an orange blossom odor." - Lafcadio Hearn

"For me chemistry represented an indefinite cloud of future potentialities which enveloped my life to come in black volutes torn by fiery flashes, like those which had hidden Mount Sinai. Like Moses, from that cloud I expected my law, the principle of order in me, around me, and in the world. I would watch the buds swell in spring, the mica glint in the granite, my own hands, and I would say to myself: I will understand this, too, I will understand everything." - Primo Levi

"There's nothing colder than chemistry." - Anita Loos

 
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