THERMODYNAMIC PARAMETERS FOR THE FORMATION OF GLYCINE COMPLEXES WITH MAGNESIUM(II), CALCIUM(II), LEAD(II), MANGANESE(II), COBALT(II), NICKEL(II), ZINC(II) AND CADMIUM(II) AT DIFFERENT TEMPERATURES AND IONIC STRENGTHS, WITH PARTICULAR REFERENCE TO NATURAL FLUID CONDITIONS
A. Casale et al., THERMODYNAMIC PARAMETERS FOR THE FORMATION OF GLYCINE COMPLEXES WITH MAGNESIUM(II), CALCIUM(II), LEAD(II), MANGANESE(II), COBALT(II), NICKEL(II), ZINC(II) AND CADMIUM(II) AT DIFFERENT TEMPERATURES AND IONIC STRENGTHS, WITH PARTICULAR REFERENCE TO NATURAL FLUID CONDITIONS, Thermochimica acta, 255, 1995, pp. 109-141
Protonation constants and Mg2+-, Ca2+-, Pb2+-, Mn2+-, Co2+-, Ni2+-, Cu
2+-, Zn2+- and Cd2+-glycine complex formation constants have been dete
rmined in different aqueous media at different temperatures. Salt effe
cts are explained by a complex formation model which takes into accoun
t the formation of weak species. From the temperature dependence of th
e formation constants, thermodynamic parameters Delta H-Kelvin (and in
some cases Delta C-p(Kelvin)) have been obtained. A rigorous analysis
of literature data, together with experimental findings, allows recom
mended formation parameters, in the ranges 0 less than or equal to I-e
less than or equal to 1 mol l(-1) (I-e is the effective ionic strengt
h) and 5 degrees C less than or equal to T less than or equal to 45 de
grees C, to be obtained. Because the proposed model can be used in any
electrolyte mixture in the above I and T ranges, the speciation in se
awater, and other natural fluids, can be simulated by appropriate comp
uter programs. The validity of the present approach which takes into a
ccount the ionic strength dependence of formation constants, together
with the concepts of effective ionic strength and complex formation mo
del, is discussed.