Vapour pressures and activities in the reciprocal fused salt systems ZnCl2 + Na2SO4 and ZnSO4 + NaCl

1975 ◽  
Vol 28 (12) ◽  
pp. 2587 ◽  
Author(s):  
RG Anthony ◽  
H Bloom

Zinc chloride vapour pressures, activities and partial molar energies have been determined in the reciprocal fused salt system: Zn,Na/Cl,SO4 over the range 770-900 K. The transpiration vapour pressure of pure ZnCl2 was first redetermined for the range 720-900 K and found to follow the equation (in which P� is in mmHg): �������������� Log P�ZnCl2 = (-8247�17)/T-5.033 log T + 26.213 � 0.006 Activities of ZnC1, in the reciprocal system differed greatly from ideality, the degree of departure varying with both composition and temperature. In general, at relatively high ZnCl, concentrations, observed activities were greater than ideal and ZnCl2 partial molar enthalpies were positive; this behaviour is believed to be largely caused by the effect of partial covalent bonding in pure ZnCl2. At low ZnCl2 concentrations, activities were much less than ideal and ZnCl2 partial molar enthalpies were negative; this other effect is believed to be caused by the formation of complex ions within this system.

1970 ◽  
Vol 23 (3) ◽  
pp. 501 ◽  
Author(s):  
H Bloom ◽  
TH Spurling ◽  
J Wong

Vapour pressure measurements were made by a transpiration method for molten zinc chloride and molten mixtures of this salt with sodium and potassium chlorides, respectively. Activities of zinc chloride in the mixtures were calculated and from these values, those of the alkali chloride were calculated by Gibbs-Duhem integration. For this purpose a convenient computer method has been devised. Although the large deviations of activity and activity coefficients qualitatively support independent evidence that complex ions are formed in these systems, the results cannot quantitatively be explained using a calculation due to Braunstein in terms of interactions in the melt to form complex ions of a unique type, e.g. ZnCl3- or ZnCl42- etc. This indicates that the departure from ideal behaviour needs to be explained by a more detailed theory.


1959 ◽  
Author(s):  
R.A. Osteryoung ◽  
J.D. VanNorman ◽  
J.H. Christie

1952 ◽  
Vol 74 (7) ◽  
pp. 1760-1762 ◽  
Author(s):  
R. E. Wood ◽  
H. L. Ritter
Keyword(s):  
X Ray ◽  

1989 ◽  
Vol 161 (Part_1_2) ◽  
pp. 239-243
Author(s):  
Rolf Edelmann ◽  
Konrad G. Weil
Keyword(s):  

1981 ◽  
Vol 34 (3) ◽  
pp. 479 ◽  
Author(s):  
H Bloom ◽  
MS White

The electromotive forces of galvanic cells for the formation of PbBr2 in the molten binary salt systems, PbBr2-KBr, PbBr2,-RbBr and PbBr2-CsBr, have been measured. Activities, activity coefficients and partial molar free energies have been calculated for each component of the three systems. Integral free energies of mixing have also been calculated. Various models of mixing of molten salts have been applied to the results. The systems contain complex ions, probably mixtures of PbBr42-, PbBr64- with some PbBr3-.


1961 ◽  
Vol 65 (11) ◽  
pp. 2026-2028 ◽  
Author(s):  
William A. Barber ◽  
Carol L. Sloan

1976 ◽  
Vol 29 (9) ◽  
pp. 2069
Author(s):  
RG Anthony ◽  
H Bloom

Activities of PbCl2 in the molten system K2SO4+PbCl2 have been measured at 1012 K by a transpiration vapour pressure method. Values of PbCl2 activities are calculated from the conformal ionic solution model (CIS), the result being in reasonable agreement with experimentally measured values. Results obtained may therefore be summarized by the CIS equation APbCl2 = xpb(xcl)2exp[0.2405/T)(X?k)2{-3285-X?pb(11564+2032(3X?k-1))}] where Xi, X?t are ion fractions and equivalent ion fractions respectively.


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