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Mischungswärmen und Verbindungsbildung in binären flüssigen Systemen. III. Äther - Chloroform-Systeme

  • The enthalpies of mixing at 25° of diethyl ether, di-n-propyl ether, di-n-butyl ether, di-isopropyl ether, propylene oxide, tetrahydrofuran, and tetrahydropyran with chloroform are determined by an isothermal titration method. As a result, the functions HM-f(N CHCl3) are obtained with a step width of 0.025 of the mole fraction and a relative accuracy of 1 per cent or better. Evaluation of the heat of mixing data by means of equilibrium models ("ideal associated mixture") shows that the systems of aliphatic ethers with chloroform behave rather precisely as one-step equilibria of the type A + B = AB (A = ether; B = chloroform). In the systems of cyclic ethers with chloroform, a se­cond equilibrium step, AB + B = AB2 , must be considered, the importance of which decreases with increasing ring size of the ether. The equilibrium data calculated for the seven ether-diloroform systems are discussed.

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Metadaten
Author:Friedrich BeckerGND, Michael Kiefer
URN:urn:nbn:de:hebis:30:3-740433
DOI:https://doi.org/10.1515/zna-1971-0617
ISSN:1865-7109
Parent Title (German):Zeitschrift für Naturforschung, A
Publisher:Verlag der Zeitschrift für Naturforschung
Place of publication:Tübingen
Document Type:Article
Language:German
Date of Publication (online):2014/06/02
Year of first Publication:1971
Publishing Institution:Universitätsbibliothek Johann Christian Senckenberg
Release Date:2023/06/26
Volume:26
Issue:6
Page Number:7
First Page:1040
Last Page:1046
HeBIS-PPN:510487998
Institutes:Biochemie, Chemie und Pharmazie / Biochemie und Chemie
Dewey Decimal Classification:5 Naturwissenschaften und Mathematik / 54 Chemie / 540 Chemie und zugeordnete Wissenschaften
Sammlungen:Universitätspublikationen
Licence (German):License LogoCreative Commons - Namensnennung-Nicht kommerziell-Keine Bearbeitung 3.0