Activity coefficients of LiCl in (PEG 4000+water) at T = (288.15, 298.15, and 308.15) K

被引:23
作者
Morales, Jaime W. [2 ]
Galleguillos, Hector R. [2 ]
Graber, Teofilo A. [2 ]
Hernandez-Luis, Felipe [1 ]
机构
[1] Univ La Laguna, Dept Quim Fis, Tenerife, Spain
[2] Univ Antofagasta, Ctr Invest Cient & Tecnol Mineria, Dept Ingn Quim, Antofagasta, Chile
关键词
LiCl; PEG; 4000; emf; Ion-selective electrode (ISE); Activity coefficient; AQUEOUS 2-PHASE SYSTEMS; EPSILON-INCREASING COSOLVENT; IMPROVED ISOPIESTIC METHOD; LIQUID-LIQUID EQUILIBRIA; FORMAMIDE-WATER MIXTURES; PLUS WATER; CELL H2(PT)-HCL-AGCL-AG; POLY(ETHYLENE GLYCOL); VIRIAL EQUATION; PHASE-DIAGRAMS;
D O I
10.1016/j.jct.2010.05.001
中图分类号
O414.1 [热力学];
学科分类号
摘要
The electromotive force of the cell containing two ion-selective electrodes (ISE), Na-ISE vertical bar LiCl (m). PEG 4000 (w), H2O (1 - w)vertical bar CI-ISE has been measured at temperatures of (288.15, 298 15, and 308.15) K as a function of the mass fraction of PEG 4000 (w) in the mixture. w was varied between 0 and 025 in 0.05-unit steps and the molality of the electrolyte (m) was between c.a. (0 03 and 5 8) mol kg(-1) The values of the standard electromotive force. E degrees. were determined using routine methods of extrapolation, together with extended Debye-Huckel and Pitzer equations. The results obtained produced good internal consistency for all the temperatures studied Once E was determined, the mean ionic activity coefficients for LiCl, the Gibbs free energy of transfer from the water to (PEG 4000 + water), and the primary LiCl hydration number were calculated. (C) 2010 Elsevier Ltd All rights reserved
引用
收藏
页码:1255 / 1260
页数:6
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