Pub Date : 2023-12-08DOI: 10.1007/s10698-023-09491-w
K. Brad Wray
It is widely recognized that conceptual and theoretical innovations and the employment of new instruments and experimental techniques are important factors in explaining the growth of scientific knowledge in chemistry. This study examines another dimension of research in chemistry, collaboration and co-authorship. I focus specifically on Theodore Richards’ career and publications. During the period in which Richards worked, co-authorship was beginning to become more common than it had been previously. Richards was the first American chemist to be awarded a Nobel Prize and he was at the forefront in this new trend in chemistry. He collaborated more than was typical for his time, with many scientists, in different sized groups, and he often had persistent collaborative relationships, extending over a number of years. Further, it appears that these collaborations benefited Richards, his collaborators, and the field of chemistry as a whole.
{"title":"Co-authorship in chemistry at the turn of the twentieth century: the case of Theodore W. Richards","authors":"K. Brad Wray","doi":"10.1007/s10698-023-09491-w","DOIUrl":"10.1007/s10698-023-09491-w","url":null,"abstract":"<div><p>It is widely recognized that conceptual and theoretical innovations and the employment of new instruments and experimental techniques are important factors in explaining the growth of scientific knowledge in chemistry. This study examines another dimension of research in chemistry, collaboration and co-authorship. I focus specifically on Theodore Richards’ career and publications. During the period in which Richards worked, co-authorship was beginning to become more common than it had been previously. Richards was the first American chemist to be awarded a Nobel Prize and he was at the forefront in this new trend in chemistry. He collaborated more than was typical for his time, with many scientists, in different sized groups, and he often had persistent collaborative relationships, extending over a number of years. Further, it appears that these collaborations benefited Richards, his collaborators, and the field of chemistry as a whole.</p></div>","PeriodicalId":568,"journal":{"name":"Foundations of Chemistry","volume":"26 1","pages":"75 - 88"},"PeriodicalIF":1.8,"publicationDate":"2023-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138559768","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-12-08DOI: 10.1007/s10698-023-09493-8
Curt Wentrup
Compelling evidence is presented that Glauber worked as a laborator (laboratory assistant) for Landgrave Georg of Hesse-Darmstadt from 1632/33 till he was appointed apothecary in Giessen in 1635. During this time, he was also used as laborator by the landgrave’s personal physician, Helwig Dieterich. Glauber became a famous chemist, whose alchemical secrets were keenly solicited by King Frederik III of Denmark, Queen Christina of Sweden, and, according to the 1662 diary of Ole Borch, King Charles II of England. A 1689 letter to Queen Christina contains detailed descriptions of Glauber’s alkahest, his decomposition and redintegration of saltpeter, and his ‘most secret sal armoniacum’, which is interpreted here for the first time.
{"title":"Johann Rudolph Glauber: the royals’ alchemist and his secret recipes","authors":"Curt Wentrup","doi":"10.1007/s10698-023-09493-8","DOIUrl":"10.1007/s10698-023-09493-8","url":null,"abstract":"<div><p>Compelling evidence is presented that Glauber worked as a <i>laborator</i> (laboratory assistant) for Landgrave Georg of Hesse-Darmstadt from 1632/33 till he was appointed apothecary in Giessen in 1635. During this time, he was also used as <i>laborator</i> by the landgrave’s personal physician, Helwig Dieterich. Glauber became a famous chemist, whose alchemical secrets were keenly solicited by King Frederik III of Denmark, Queen Christina of Sweden, and, according to the 1662 diary of Ole Borch, King Charles II of England. A 1689 letter to Queen Christina contains detailed descriptions of Glauber’s alkahest, his decomposition and redintegration of saltpeter, and his ‘most secret sal armoniacum’, which is interpreted here for the first time.</p></div>","PeriodicalId":568,"journal":{"name":"Foundations of Chemistry","volume":"26 1","pages":"3 - 13"},"PeriodicalIF":1.8,"publicationDate":"2023-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138552598","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-11-25DOI: 10.1007/s10698-023-09488-5
Alessio Rocci
Théophile De Donder, a Belgian mathematician born in Brussels, elaborated two important ideas that created a bridge between thermodynamics and chemical kinetics. He invented the concept of the degree of advancement of a reaction, and, in 1922, he provided a precise mathematical form to the already known chemical affinity by translating Clausius’s uncompensated heat into formal language. These concepts merge in an important inequality that was the starting point for the formalization of non-equilibrium thermodynamics. The present article aims to reconstruct how De Donder elaborated his ideas and developed them by exploring his teaching activity and its connection with his scientific production. Furthermore, it emphasizes the role played by the discussions with his disciples who became his collaborators. The paper analyzes De Donder’s efforts in participating in the second Solvay Chemistry Council in 1925 to call the attention of chemists to his mathematical approach. We explain why his work did not receive much attention at the time, and how, despite this, his formalization of chemical affinity became the basis for the birth of the so-called Brussels school of thermodynamics.
thachiile De Donder,一位出生于布鲁塞尔的比利时数学家,阐述了两个重要的思想,在热力学和化学动力学之间架起了一座桥梁。他发明了反应推进度的概念,并且在1922年,他通过将克劳修斯的无补偿热翻译成形式语言,为已知的化学亲和性提供了精确的数学形式。这些概念融合在一个重要的不等式中,这个不等式是形式化非平衡态热力学的起点。本文旨在通过探索德·东德尔的教学活动及其与科学成果的联系,重构他是如何阐述和发展他的思想的。此外,它强调与他的弟子讨论所起的作用,他们成为他的合作者。本文分析了德·唐德尔参加1925年第二届索尔维化学理事会的努力,以引起化学家对他的数学方法的注意。我们解释了为什么他的工作在当时没有受到太多关注,以及尽管如此,他的化学亲和的形式化如何成为所谓的布鲁塞尔热力学学派诞生的基础。
{"title":"Celebrating the birth of De Donder’s chemical affinity (1922–2022): from the uncompensated heat to his Ave Maria","authors":"Alessio Rocci","doi":"10.1007/s10698-023-09488-5","DOIUrl":"10.1007/s10698-023-09488-5","url":null,"abstract":"<div><p>Théophile De Donder, a Belgian mathematician born in Brussels, elaborated two important ideas that created a bridge between thermodynamics and chemical kinetics. He invented the concept of the degree of advancement of a reaction, and, in 1922, he provided a precise mathematical form to the already known chemical affinity by translating Clausius’s uncompensated heat into formal language. These concepts merge in an important inequality that was the starting point for the formalization of non-equilibrium thermodynamics. The present article aims to reconstruct how De Donder elaborated his ideas and developed them by exploring his teaching activity and its connection with his scientific production. Furthermore, it emphasizes the role played by the discussions with his disciples who became his collaborators. The paper analyzes De Donder’s efforts in participating in the second Solvay Chemistry Council in 1925 to call the attention of chemists to his mathematical approach. We explain why his work did not receive much attention at the time, and how, despite this, his formalization of chemical affinity became the basis for the birth of the so-called <i>Brussels school of thermodynamics</i>.</p></div>","PeriodicalId":568,"journal":{"name":"Foundations of Chemistry","volume":"26 1","pages":"37 - 73"},"PeriodicalIF":1.8,"publicationDate":"2023-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138518609","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-11-15DOI: 10.1007/s10698-023-09490-x
Klaus Ruthenberg
{"title":"Centenary Workshop on the Bifurcation of Acidity -Protonism vs. Electronism","authors":"Klaus Ruthenberg","doi":"10.1007/s10698-023-09490-x","DOIUrl":"10.1007/s10698-023-09490-x","url":null,"abstract":"","PeriodicalId":568,"journal":{"name":"Foundations of Chemistry","volume":"26 2","pages":"193 - 196"},"PeriodicalIF":1.8,"publicationDate":"2023-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s10698-023-09490-x.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136229693","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-10-21DOI: 10.1007/s10698-023-09485-8
Pieter Thyssen
Are acids natural kinds? Or are they merely relevant kinds? Although acidity has been one of the oldest and most important concepts in chemistry, surprisingly little ink has been spilled on the natural kind question. I approach the question from the perspective of microstructural essentialism. After explaining why both Brønsted acids and Lewis acids are considered functional kinds, I address the challenges of multiple realization and multiple determination. Contra Manafu and Hendry, I argue that the stereotypical properties of acids are not multiply realized. Instead, given the equivalence between the proton-donating and electron-accepting mechanisms of Brønsted and Lewis, respectively, I show that acidity as a property type can be identified with a unique microstructural property, namely the presence of a LUMO or other low energy empty orbital. In doing so, I defend the view that the Lewis theory encompasses Brønsted–Lowry, and that all Brønsted acids are also Lewis acids. Contra Hacking and Chang, I thus maintain that the different concepts of acidity do not crosscut, and that the hierarchy requirement is met. Finally, by characterizing natural kinds as powerful objects and by adopting a dispositional view of functions, I illustrate how the microessentialist can make sense of the latent and relational character of most acids. In sum, I contend that acids are genuine natural kinds, even for the microstructural essentialist.
{"title":"Are acids natural kinds?","authors":"Pieter Thyssen","doi":"10.1007/s10698-023-09485-8","DOIUrl":"10.1007/s10698-023-09485-8","url":null,"abstract":"<div><p>Are acids natural kinds? Or are they merely relevant kinds? Although acidity has been one of the oldest and most important concepts in chemistry, surprisingly little ink has been spilled on the natural kind question. I approach the question from the perspective of microstructural essentialism. After explaining why both Brønsted acids and Lewis acids are considered functional kinds, I address the challenges of multiple realization and multiple determination. Contra Manafu and Hendry, I argue that the stereotypical properties of acids are not multiply realized. Instead, given the equivalence between the proton-donating and electron-accepting mechanisms of Brønsted and Lewis, respectively, I show that acidity as a property type can be identified with a unique microstructural property, namely the presence of a LUMO or other low energy empty orbital. In doing so, I defend the view that the Lewis theory encompasses Brønsted–Lowry, and that all Brønsted acids are also Lewis acids. Contra Hacking and Chang, I thus maintain that the different concepts of acidity do not crosscut, and that the hierarchy requirement is met. Finally, by characterizing natural kinds as powerful objects and by adopting a dispositional view of functions, I illustrate how the microessentialist can make sense of the latent and relational character of most acids. In sum, I contend that acids are genuine natural kinds, even for the microstructural essentialist.</p></div>","PeriodicalId":568,"journal":{"name":"Foundations of Chemistry","volume":"26 2","pages":"225 - 253"},"PeriodicalIF":1.8,"publicationDate":"2023-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135512875","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-10-18DOI: 10.1007/s10698-023-09484-9
Klaus Ruthenberg
In this short essay I address the central topic of the Centenary Workshop on Acidity, that is the relations of the classical protonist acid–base theory by Brønsted and the electronist approach by Lewis. Emphasis is laid on the empirical background of both approaches and the over-theoretization of chemical phenomena (essentialism) is criticized.
{"title":"Bifurcations","authors":"Klaus Ruthenberg","doi":"10.1007/s10698-023-09484-9","DOIUrl":"10.1007/s10698-023-09484-9","url":null,"abstract":"<div><p>In this short essay I address the central topic of the Centenary Workshop on Acidity, that is the relations of the classical protonist acid–base theory by Brønsted and the electronist approach by Lewis. Emphasis is laid on the empirical background of both approaches and the over-theoretization of chemical phenomena (essentialism) is criticized.</p></div>","PeriodicalId":568,"journal":{"name":"Foundations of Chemistry","volume":"26 2","pages":"213 - 224"},"PeriodicalIF":1.8,"publicationDate":"2023-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s10698-023-09484-9.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135885168","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-10-10DOI: 10.1007/s10698-023-09489-4
Eric R. Scerri
{"title":"Editorial 75","authors":"Eric R. Scerri","doi":"10.1007/s10698-023-09489-4","DOIUrl":"10.1007/s10698-023-09489-4","url":null,"abstract":"","PeriodicalId":568,"journal":{"name":"Foundations of Chemistry","volume":"25 3","pages":"341 - 342"},"PeriodicalIF":0.9,"publicationDate":"2023-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136254560","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-10-04DOI: 10.1007/s10698-023-09482-x
Gerd-Uwe Flechsig
Among the many acid-base concepts, the theory of Usanovich is one of the least known despite the most general scope including almost all chemical reaction types and even redox chemistry. Published 1939 in a Soviet journal in Russian language, it gained little immediate attention, and was later criticized mainly as being too broad in scope. Although several articles recently remembered Usanovich and his acid–base theory, one major inconsistency again was overseen: the electron is put in a row along with anions. Chemical history probably correctly puts this concept aside, also because it added little explanation capabilities beyond the elaborated considerations of the simultaneously published acid–base theory of Gilbert N. Lewis which was later refined by Pearson (hard and soft acids and bases, “HSAB”). A modified version of the core of Usanovich' concept is finally discussed. It combines the classic protic and aprotic acid–base concepts on the foundations of Lewis’ and Pearsons ideas.
在众多酸碱概念中,乌萨诺维奇的理论是最不为人所知的理论之一,尽管其范围最广,几乎包括所有化学反应类型,甚至氧化还原化学。乌萨诺维奇的理论于 1939 年发表在苏联的俄文杂志上,但没有立即引起人们的注意,后来主要被批评为范围太广。尽管最近有几篇文章回忆了乌萨诺维奇和他的酸碱理论,但其中一个主要的不一致之处又被忽略了:电子与阴离子被放在了一起。化学史可能正确地将这一概念搁置一边,这也是因为除了吉尔伯特-N-刘易斯(Gilbert N. Lewis)同时发表的酸碱理论的详细考虑之外,它几乎没有增加任何解释能力,而这一理论后来被皮尔逊(Hard and Soft acids and bases,"HSAB")完善。最后讨论的是乌萨诺维奇概念核心的修正版。它在刘易斯和皮尔逊思想的基础上结合了经典的原生酸和钝化酸-碱概念。
{"title":"Usanovich and Nernst colliding: inconsistencies in the all-in-one acid–base concept?","authors":"Gerd-Uwe Flechsig","doi":"10.1007/s10698-023-09482-x","DOIUrl":"10.1007/s10698-023-09482-x","url":null,"abstract":"<div><p>Among the many acid-base concepts, the theory of Usanovich is one of the least known despite the most general scope including almost all chemical reaction types and even redox chemistry. Published 1939 in a Soviet journal in Russian language, it gained little immediate attention, and was later criticized mainly as being too broad in scope. Although several articles recently remembered Usanovich and his acid–base theory, one major inconsistency again was overseen: the electron is put in a row along with anions. Chemical history probably correctly puts this concept aside, also because it added little explanation capabilities beyond the elaborated considerations of the simultaneously published acid–base theory of Gilbert N. Lewis which was later refined by Pearson (hard and soft acids and bases, “HSAB”). A modified version of the core of Usanovich' concept is finally discussed. It combines the classic protic and aprotic acid–base concepts on the foundations of Lewis’ and Pearsons ideas.</p></div>","PeriodicalId":568,"journal":{"name":"Foundations of Chemistry","volume":"26 2","pages":"197 - 202"},"PeriodicalIF":1.8,"publicationDate":"2023-10-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s10698-023-09482-x.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135592416","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-10-03DOI: 10.1007/s10698-023-09483-w
Apostolos K. Gerontas
Acidic substances were known for thousands of years, and their macroscopic-sensory characteristics were reflected by words in most ancient languages. In the Western canon, the history of the concept of acidity goes back to Ancient Greece. In Greek, the word associated with acidity from its early literary references was ὀξύς (“sharp”), and still in contemporary Greek the words “sour” and “acidic” have the same root. This paper makes a short presentation of the appearance of the abstract concept in the works of Plato and Aristotle and relates it, on one side to the already existing theological-philosophical tradition, starting with Hesiod´s Theogony and on the other, to the then available to the Greeks organoleptic experiences of sourness-vinegar and sour milk.
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