Gibbs Energies of Transfer of Anions from Water to Mixed Aqueous Organic Solvents

ChemInform ◽  
2007 ◽  
Vol 38 (49) ◽  
Author(s):  
Yizhak Marcus
1995 ◽  
Vol 60 (4) ◽  
pp. 537-544 ◽  
Author(s):  
Vladislav Holba ◽  
Marcela Hanková

The solubilities of tris(ethylenediamine)chromium(III) and hexa(urea)chromium(III) hexacyanoferrates(III) in aqueous solutions of different supporting electrolytes as well as in binary mixtures of water with methanol, tert-butyl alcohol and acetonitrile were measured at 25 °C. The experimental data have been used to evaluate the activity coefficients of the saturating salts in water and their Gibbs energies of transfer from water into the binary mixtures investigated.


2000 ◽  
Vol 100 (3) ◽  
pp. 819-852 ◽  
Author(s):  
C. Kalidas ◽  
Glenn Hefter ◽  
Yizhak Marcus

1994 ◽  
Vol 59 (8) ◽  
pp. 1738-1744
Author(s):  
Vladislav Holba

The solubilities of tetraalkylammonium dianilinetetraisothiocyanatochromates(III) (alkyl = methyl, ethyl, 1-propyl, and 1-butyl) in water, water - methanol, water - tert-butyl alcohol and water - acetonitrile solutions were measured at 25 °C. The results were used to evaluate the activity coefficients and Gibbs energies of transfer of the saturating salts from water to the mixed systems. The Gibbs energies of transfer of the [Cr(C6H5NH2)2(NCS)4]- ion were obtained by means of known ionic transfer functions for the tetraalkylammonium ions based on the TATB assumption.


1989 ◽  
Vol 67 (8) ◽  
pp. 1268-1273 ◽  
Author(s):  
Mahmoud Mohamad Elsemongy ◽  
Ahmed Ahmed Abdel-Khalek

The standard absolute potentials of hydrogen, Ag–AgX (X = Cl, Br, and I) and M/M+ (M = Li, Na, K, Rb, and Cs) electrodes in nine different acetone + water solvents containing up to 80 wt. % acetone were determined from the emf data at 25 °C of the cells: glass electrode/HCl (m), solvent/AgCl–Ag and glass electrode (M)/MX (m), solvent/AgX–Ag. The standard Gibbs free energies of a transfer of halogen acids and alkali metal halides as well as their constituent individual ions from water to the respective solvents were computed. The observed increases in [Formula: see text] values of all ions with increasing acetone content of the solvent and their relative order in each solvent were interpreted and discussed. A comparison of the present results with those obtained earlier in the dimethyl sulphoxide (DMSO) + water solvents shows the different nature of the two dipolar aprotic solvents, acetone and DMSO, in their aqueous mixtures. Keywords: acetone + water solvents, electrode potentials, emf measurements, individual ions, transfer free energies.


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