Determination of the transfer thermodynamic functions for some monovalent ions from water to N,N′-dimethylpropyleneurea

2001 ◽  
Vol 3 (23) ◽  
pp. 5248-5254 ◽  
Author(s):  
Pavel Smirnov ◽  
Linhong Weng ◽  
Ingmar Persson
2019 ◽  
Vol 55 (10) ◽  
pp. 978-988
Author(s):  
E. V. Kuz’mina ◽  
E. V. Karaseva ◽  
N. V. Chudova ◽  
A. A. Mel’nikova ◽  
V. S. Kolosnitsyn

2004 ◽  
Vol 218 (5) ◽  
pp. 515-550 ◽  
Author(s):  
Ranjana Bhattacharyya ◽  
S. C. Lahiri

AbstractSingle ion Gibbs energies of monovalent ions in fourteen solvents (water, methanol, NMF, PC, ethanol, n-propanol, iso-propanol, n-butanol, t-butanol, ethylene glycol, acetone, THF, 1,4-dioxan, acetonitrile) with or without (ion–dipole, ion–induced dipole, ion–quadrupole) interactions were determined. The basicity of the solvents was determined from the absolute values of ΔG0solvation(H+) or ΔG0solution(H+) based on single standard state utilising the modified Born equation suggested by Lahiri. The method involves no arbitrary assumptions. A single scale for the absolute electrode potentials (E0 values) has been determined based on calculated Gibbs energies of solvation or solution of single ions. Appropriation of Gibbs energies of solvation of electrolytes into single ion values is not possible. Gibbs energies of formation of electrolytes in solvents must be taken into consideration. Stabilisation energies of electrolytes (MX) in solvents akin to lattice energies in solids were determined.


1997 ◽  
Vol 48 (2) ◽  
pp. 327-329 ◽  
Author(s):  
Lu Chengxue ◽  
Yu Xiufang ◽  
Zhang Honglin

2013 ◽  
Vol 113 (17) ◽  
pp. 173515
Author(s):  
P. Roura ◽  
F. Taïr ◽  
J. Farjas ◽  
P. Roca i Cabarrocas

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