<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Grigore, L.a , Meghea, A.b , Grigore, O.c , Martins, R.a</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Thermodynamic properties of ternary aqueous electrolyte solutions</style></title><secondary-title><style face="normal" font="default" size="100%">Physics and Chemistry of Liquids</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">1999</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.scopus.com/inward/record.uri?eid=2-s2.0-0033379283&amp;partnerID=40&amp;md5=7b7aba93774abf157a0b942086554bdb</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">4</style></number><volume><style face="normal" font="default" size="100%">37</style></volume><pages><style face="normal" font="default" size="100%">409-428</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;In previous papers the mean excess chemical potential, μ1(E), in ternary systems of the type I sulphate + II sulphate + H2O, at 25°C was determined. Results obtained for systems with CuSO4(I), and ZnSO4(I) respectively, pointed out an obvious disparity between their behaviours. They show the existence of some important association phenomena partially accounting for the substantial deviations from ideal behaviour. The ternary sulphate systems (CuSO4 + Me(I,II)SO4 + H2O; ZnSO4 + Me(I,II)SO4 + H2O) studied were characterized against the binaries of the same ionic strength, experimental data being obtained using both e.m.f. and spectrophotometric methods. Deviations from the ideal behaviour were discussed in terms of thermodynamic excess functions and association constants. A comparative study between the results obtained with the two above mentioned methods is presented. In previous papers the mean excess chemical potential, μ1 E, in ternary systems of the type I sulphate+II sulphate+H2O, at 25 °C was determined. Results obtained for systems with CuSO4(I), and ZnSO4(I) respectively, pointed out an obvious disparity between their behaviours. They show the existence of some important association phenomena partially accounting for the substantial deviations from ideal behaviour. The ternary sulphate systems (CuSO4+MeI, IISO4+H2O; ZnSO4+MeI, IISO4+H2O) studied were characterized against the binaries of the same ionic strength, experimental data being obtained using both e.m.f. and spectrophotometric methods. Deviations from the ideal behaviour were discussed in terms of thermodynamic excess functions and association constants. A comparative study between the results obtained with the two above mentioned methods is presented.&lt;/p&gt;
</style></abstract><notes><style face="normal" font="default" size="100%">&lt;p&gt;cited By 0&lt;/p&gt;
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