Textual Alchemy: The Transformation of Pseudo-Albertus Magnus's Semita Recta into the Mirror of Lights

Abstract

This article explores the strategies of and the reasons behind the reworking of pseudo-Albertus Magnus's Semita recta into the Mirror of Lights. I argue that the redactor sought to provide a more comprehensive defence of the legitimacy of alchemy than found in the Semita recta. In the process of doing so, he reshaped the original text so as to present three units that addressed different parts of the alchemical opus: first, theory and justification of alchemy; second, basic information on substances and procedures; and, third, practice. The redactor employed sophisticated textual tools identical to those seen in scholastic texts. These strategies, I argue, constitute part of the redactor's attempt to bring authority and credibility to his project and to alchemy in general. Certainly, much more attention needs to be paid to these experiments of textual alchemy in order to understand the practice of alchemy in the late medieval period.     

Essay Reviews

Abstract

Liebig's 1831 paper that describes a new apparatus for the analysis of organic compounds and the results of several analyses using the apparatus is a justly famous contribution to the evolution of modern chemistry. In this paper, I look at the three separate components of Liebig's combustion apparatus that collect the water, carbon dioxide and nitrogen released by the combustion of six alkaloids. Gravimetric data included in the paper reveal that very accurate results could be obtained for water by absorption in a calcium chloride tube, and even better results for carbon dioxide resulted from use of the Kaliapparat. Volumetric measurement of nitrogen gave very poor results despite Liebig's efforts to improve it. Inaccuracies in nitrogen measurement made consistent construction of accurate molecular formulae for nitrogenous substances impossible, and only fortuitous decisions intended to bring molecular formulae into agreement with measured combining weights gave formulae in agreement with modern ones, as in the case for quinine.     

Historical Roots of the "Mad Scientist": Chemists in Nineteenth-century Literature

Abstract

This paper traces the historical roots of the "mad scientist," a concept that has powerfully shaped the public image of science up to today, by investigating the representations of chemists in nineteenth-century Western literature. I argue that the creation of this literary figure was the strongest of four critical literary responses to the emergence of modern science in general and of chemistry in particular. The role of chemistry in this story is crucial because early nineteenth-century chemistry both exemplified modern experimental laboratory research and induced, due to its rapid growth, a ramification and fragmentation of knowledge that undermined former ideals of the unity of knowledge under the umbrella of metaphysics and religion. Because most writers considered contemporary chemistry an offspring of "wrong alchemy," all four responses drew on the medieval literary figure of the "mad alchemist" to portray chemists. Whereas early writers considered the quest for scientific knowledge to be altogether in vain, later writers pointed out the narrow-minded goals and views specifically of chemistry. A third response moved that criticism to a metaphysical and religious level, by relating chemistry to materialism, nihilism, atheism and hubris. The fourth response, the "mad scientist," elaborated on the hubris theme by attaching moral perversion to the "mad alchemist."     

Enlightenment Chemistry Translated by a Brazilian Man of Science in Lisbon

Abstract

The Brazilian-born man of science Martim Francisco de Andrada (1775–1844) actively participated in some of the major publishing activities of the Portuguese Enlightenment, notably in the Arco do Cego printing house. For many Brazilians, technical and scientific activities provided a path to becoming part of the administrative system of the Portuguese Empire. This paper examines Andrada’s work as translator of Torbern Bergman’s book Sciagraphia Regni Mineralis, secundum principia proxima digesti, originally published in Latin in 1782 and soon translated into French. A comparison between the Portuguese and French editions allows us to understand the different ways in which translators intervened in texts. Martim Francisco established a dialogue both with Bergman and with his translators, Jean-André Mongez and Jean-Claude Delamétherie, in addition to the challenge of having to deal with the propositions set forward by the new pneumatic chemistry. We argue that the Brazilian translator’s main objective was to explore the possibilities of using the book as a teaching and fieldwork manual. From this perspective, the resulting translation gains significance when read at the confluence of these demands and intentions.     

Nehemiah Grew (1641–1712) and the Saline Chymistry of Plants

Abstract

In a series of lectures appended to his magisterial Anatomy of Plants (1682), Nehemiah Grew (1641–1712) explained the results of his own research into the saline chemistry of plants, following an established tradition in early modern chemistry. Members of the Royal Society such as Daniel Coxe were heavily involved in researching salt chemistry in the latter part of the seventeenth century, analysing the role of salts in spa waters, physiology, and as a fundamental element in iatrochemistry. Such researches of Royal Society members were often based upon the chemistry of Johann Van Helmont (1577–1634). As this paper will demonstrate, Grew's work drew from his microscopic research to elaborate and question some of Coxe's and hence Van Helmont's ideas about the principles of matter. Grew also used the results of his chemical research to draw conclusions about plant structure and colour, and applied his results to other areas in natural history such as meteorology, illustrating that chemistry was the basic analytical tool for seventeenth-century investigators of anatomy and natural history.     

Establishing the Canon: George Ripley and his Alchemical Sources

Abstract

George Ripley, Canon of Bridlington (ca. 1415 to ca. 1490) was one of England's most famous alchemists, whose alchemical opera attracted study and commentary throughout the sixteenth and seventeenth centuries, and were printed and translated both in England and abroad. Yet Ripley's frequently baffling texts have proved resistant to scholarly interpretation. This paper attempts to unravel some of Ripley's alchemical theories and practice, firstly by identifying his major sources, and secondly by gauging his response to these texts. For instance, although Ripley's interest in the corpus of alchemical texts pseudonymously attributed to Ramon Lull is well documented, it transpires that his best known work, the Compound of Alchemy, or Twelve Gates, is actually based not on a Lullian work, but on a Latin treatise that Ripley attributed to the little-known alchemist, Guido de Montanor. Further clues to Ripley's alchemical thought can be obtained by considering his handling of a potential conflict between his two authorities, Lull and Guido. The resulting insights into Ripley's alchemy provide an instrument for assessing which of Ripley's pseudoepigraphic works can be truly called "canonical".     

Emil Wohlwill's “Entdeckung des Isomorphismus”: A Nineteenth-Century “Material Biography” of Crystallography

Abstract

Eilhard Mitscherlich's experimental work on isomorphism in the crystallisation of many inorganic compounds was regarded by Emil Wohlwill (1835–1912) as a milestone in the history of the atomic–molecular theory. Despite his positivist account, Wohlwill's 1866 survey was primarily concerned with the material conditions that shaped Mitscherlich's theoretical assumptions on iso- and polymorphic crystallisation, narrowing the range of possible alternative models. Following an account of Wohlwill's exposition, and a discussion of his historiographic views, the paper shows how, from a historico-epistemological perspective, technical improvements in crystallography (an emerging branch of early-nineteenth-century mineralogy) were deeply entangled with a new interest in crystal formation as a cutting-edge research field of inorganic chemistry. This had fundamental implications for the development of atomic and molecular theory.     

Estimation of Aluminum Speciation in Surface Waters of Low Ionic Strength by a Simple Computer Model

Abstract

A simple computer model based on chemical equilibrium calculation for evaluating the aluminum speciation in surface waters of low ionic strength (I < 1 × 10^?4 M) was presented in this paper. The speciations of aluminum obtained by this model have been compared with those obtained experimentally and the reasons for the observed differences have been discussed. This model has been applied to the estimation of aluminum speciation in practical surface waters sampling from areas of the United Kingdom, United States and People's Republic of China. Some valuable conclusions are obtained.     

From Candles to Cabinets: “Familiar Chemistry” in Early Victorian Britain

Abstract

“Familiar chemistry” flourished in early Victorian Britain. This set of texts an practices advocated drawing scientific lessons from the habitual activities of daily life, in which the hidden chemical contents of common objects and quotidian processes were revealed. Through sensory interactions in the family environment — enlightening conversation and hands-on explorations — a wide range of phenomena could be introduced to childish bodies and minds. A close reading of texts such as Albert J. Bernays' Household Chemistry (1852), alongside a consideration of everyday artefacts, as well as novel specialist objects such as Robert Best Ede's “Youth's Laboratory” (ca. 1837–1845), allows a discussion of this educational style, and an introduction of this new analytic category. In particular, I argue, familiar chemistry succeeded by reworking the popular literary genre of the familiar introduction with an emphasis on embodied interactions with emphatically real things, and gave a central role to the familial domestic context. From candles to cabinets, and beyond, in this article I will demonstrate that familiar chemistry provides a new perspective on scientific education and participation in the nineteenth century.     

Richard Kirwan's Phlogiston Theory: Its Success and Fate

Abstract

First proposed in the early 1780s, Richard Kirwan's phlogiston theory was the most successful enunciation of the English pneumatic approach to phlogiston. Phlogiston was identified with a material substance, inflammable air. In this paper, I explore the nature of Kirwan's theory, its success in the mid-1780s, the unprecedented collective attack on Kirwan's Essay on Phlogiston by Lavoisier and his colleagues, and Kinvan's ultimate abandonment of phlogistic explanation.     

Variation in essential oil content and composition of Ridolfia segetum Moris based on 30-hour prolonged fractionated extraction procedure

Abstract

A comprehensive study on essential oil samples extracted from Ridolfia segetum Moris (Apiaceae) collected in Tarquinia (Italy) is reported. In this study, a 30-hour, fractionated, steam distillation procedure for essential oil preparation was applied. The gas chromatographic-mass spectrometry analysis showed monoterpene o-cymene and phenylpropanoid dill-apiol as the major essential oil’s constituents revealing a new chemotype dependent on extraction duration. Great impact of the duration of the distillation process on chemical profile of essential oil was observed; prolonged distillation gives chemically more diverse essential oil samples. Preliminary microbiological evaluations of the essential oils samples revealed some activity, although not high, against Candida albicans.     

Objects of inquiry in classical chemistry: material substances

I argue in the paper that classical chemistry is a science predominantly concerned with material substances, both useful materials and pure chemical substances restricted to scientific laboratory studies. The central epistemological and methodological status of material substances corresponds with the material productivity of classical chemistry and its way of producing experimental traces. I further argue that chemist??s ??pure substances?? have a history, conceptually and materially, and I follow their conceptual history from the Paracelsian concept of purity to the modern concept of pure stoichiometric compounds. The history of the concept of ??pure substances?? shows that modern chemists?? concept of purity abstracted from usefulness rather than being opposed to it. Thus modern chemists?? interest in pure chemical substances does not presuppose a concept of pure science.     

Spectrophotometric Determination of Phenols and Cyanides After Distillation from Natural Waters

Abstract

Total phenols were determined by molecular spectrophotometry, after distillation, complexation with 4-aminoantipyrine and extraction into chloroform. Cyanides were also determined spectrophotometrically after distillation from the acidified samples, and complexation in moderate acidic solution with barbituric acid. The dynamic ranges were 0 – 100 μg L^?1 for total phenols and 0 – 30 μg L^?1 for cyanides. The above methods were applied in the analysis of river, lake and stream waters collected from Northern Greece. The seasonal and spatial variation of concentrations was evaluated by two-way ANOVA. Background levels (4 – 12 μg L^?1 for total phenols and 0.3 – 3 μg L^?1 for cyanides), were found in almost all surface waters, with some exceptions.     

Synthesis,structure, and characterization of a silver(I) coordination polymer with μ6-bridging 2,2′-bipyridyl-3,3′-dicarboxylate

A silver(I) coordination polymer, [Ag₂(bpdc)] _n (1) (H₂bpdc = 2,2′-bipyridyl-3,3′-dicarboxylic acid), has been synthesized and characterized. Compound 1 exhibits a 2-D network containing 1-D channels. Each (bpdc)^2? is an octadentate μ₆-1igand coordinating with six Ag(I)'s in 1. This coordination of (bpdc)^2? ligand is first observed here. Neighboring networks are arranged in a [ABAB···] pattern to form 3-D supramolecular architecture by π···π stacking. Compound 1 shows intense photoluminescence at room temperature.     

Ionic Distribution Coefficients and Electrochemical Potentials

Abstract

A novel “electrochemical ionic distribution coefficient”, i is defined based on Guggenheim's electrochemical potential concept. i correlates the activities of a given ion in different solvents. The definition of i is entirely consistent with the practice to interrelate chemical equilibrium constants in various solvents via the classical ionic distribution coefficient i.     

丝印电极法体外筛选黄嘌呤氧化酶抑制剂方法研究

建立丝印电极快速筛选黄嘌呤氧化酶(XO)抑制剂的新方法. 利用丝网印刷技术制作一次性使用的丝印碳糊电极, 采用吸附法将羧基化的多壁碳纳米管(MWNTs)修饰在电极表面, 建立测定尿酸(UA)的简单快捷的计时电流分析方法, 将该法应用于XO抑制剂的体外筛选. 在0.3 V (vs. Ag/AgCl)的工作电位下, UA在MWNTs修饰的丝印电极上产生灵敏的响应电流, 响应时间30 s, 测定UA的线性范围为2～300 μmol•L^－1, 线性方程为Y (μmol•L^－1)＝43.8240X (μA)－0.1592, r＝0.9998, 最低检出限为1 μmol•L^－1. 用该法对4种中药水提物进行了筛选, 相对空白对照组, 桑寄生500 μg•mL^－1浓度组有显著性差异. 该法简单、快速, 电极制作成本低, 所需仪器简单, 适用于体外大量筛选XO抑制剂.     

Cationic organoiron polyelectrolyte three‐arm stars

With nucleophilic aromatic substitution and ester condensation reactions, several new first‐generation dendrimers and star‐shaped molecules containing cationic cyclopentadienyl iron moieties were prepared. Although the solubility of the organoiron star‐shaped molecules with ether bridges in polar solvents was found to decrease with an increase in the size of the molecule, the addition of ester linkages resulted in a sharp decrease in the solubility, regardless of the size. The thermal behavior of these molecules was examined with differential scanning calorimetry and thermogravimetric analysis. The glass‐transition temperatures (T_g's) of these star‐shaped molecules ranged from 123 to 170 °C. However, the addition of the ester functionality allowed for an increase in the T_g's to 151–194 °C. The star‐shaped molecules were thermally stable up to 200 °C, above which a loss of the cationic cyclopentadienyl iron moieties occurred. Degradation of the ester chains started at 321 °C, and degradation of the ether chains started at 408 °C. Electrochemical studies of the ether star‐shaped molecules showed a reduction of the 18‐electron iron centers to 19‐electron centers. This redox system was reversible at low temperatures, whereas it was irreversible at room temperature. Moreover, an increase in the number of metal moieties caused an overlap and broadening of the redox wave. Viscosity studies showed a polyelectrolyte effect for the organoiron star‐shaped molecules. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 1382–1396, 2005     

Some Comments on the Contemporary Helmontian Renaissance

Abstract

This paper uses case studies of the cities of Nancy and Metz to demonstrate that chemistry was established as a thriving public science in the French provinces in the last decades of the old regime. It shows that physicians and apothecaries were key figures in this development. I argue that a detailed study of how such minor figures as Henry Michel du Tennetar and Pierre François Nicolas in Nancy constructed their public lives and careers can help us to a broader analysis, one that is not exclusively metropolitan, of the social, cultural, economic and political forces that shaped chemistry in France in the period of the Chemical and French Revolutions.