TY - JOUR
T1 - Activity coefficients of KCl in PEG 4000+water mixtures at 288.15, 298.15 and 308.15K
AU - Hernández-Luis, Felipe
AU - Rodríguez-Raposo, Raquel
AU - Galleguillos, Héctor R.
AU - Morales, Jaime W.
N1 - Funding Information:
The authors thank CONICYT-Chile for the support provided through Fondecyt Project No. 1070909 and the ORI (International Relations Office) of the Universidad de La Laguna for its collaboration that made the stay of Héctor R. Galleguillos possible.
PY - 2010/8
Y1 - 2010/8
N2 - The electromotive force of the cell containing two ion-selective electrodes (ISE), K-ISEvertical barKCl(m), PEG 4000(Y), H2O(100-Y)vertical barCl-ISE has been measured at temperatures of 288.15, 298.15, and 308.15K as a function of the weight percentage Y of PEG 4000 in a mixed solvent. Y was varied between 0 and 25wt.% in five-unit steps and the molality of the electrolyte (m) was between ca. 0.05molkg-1 and almost saturation. The values of the standard electromotive force were calculated using routine methods of extrapolation together with extended Debye-Hückel and Pitzer equations. The results obtained produced good internal consistency for all the temperatures studied. Once the standard electromotive force was determined, mean ionic activity coefficients for KCl, Gibbs energy of transfer from the water to PEG 4000+water mixtures, interaction parameters (gEN, hEN, sEN, cp,EN), salting constants, and the KCl primary hydration number were estimated and comparatively discussed in terms of a model of structural and electrostatic interactions with those of the LiCl and NaCl previously obtained in similar mixtures.
AB - The electromotive force of the cell containing two ion-selective electrodes (ISE), K-ISEvertical barKCl(m), PEG 4000(Y), H2O(100-Y)vertical barCl-ISE has been measured at temperatures of 288.15, 298.15, and 308.15K as a function of the weight percentage Y of PEG 4000 in a mixed solvent. Y was varied between 0 and 25wt.% in five-unit steps and the molality of the electrolyte (m) was between ca. 0.05molkg-1 and almost saturation. The values of the standard electromotive force were calculated using routine methods of extrapolation together with extended Debye-Hückel and Pitzer equations. The results obtained produced good internal consistency for all the temperatures studied. Once the standard electromotive force was determined, mean ionic activity coefficients for KCl, Gibbs energy of transfer from the water to PEG 4000+water mixtures, interaction parameters (gEN, hEN, sEN, cp,EN), salting constants, and the KCl primary hydration number were estimated and comparatively discussed in terms of a model of structural and electrostatic interactions with those of the LiCl and NaCl previously obtained in similar mixtures.
KW - Activity coefficient
KW - Emf
KW - Ion-selective electrode (ISE)
KW - KCl
KW - PEG 4000
UR - http://www.scopus.com/inward/record.url?scp=77954176784&partnerID=8YFLogxK
U2 - 10.1016/j.fluid.2010.04.012
DO - 10.1016/j.fluid.2010.04.012
M3 - Article
AN - SCOPUS:77954176784
SN - 0378-3812
VL - 295
SP - 163
EP - 171
JO - Fluid Phase Equilibria
JF - Fluid Phase Equilibria
IS - 2
ER -