Js. Preston et Ac. Dupreez, THE SOLVENT-EXTRACTION OF CADMIUM AND ZINC BY MIXTURES OF CARBOXYLIC-ACIDS ADN ALKANETHIOLS, Solvent extraction and ion exchange, 12(4), 1994, pp. 667-685
The effect of some aliphatic sulphur-containing compounds on the solve
nt extraction of cadmium and zinc by representative carboxylic acids (
HA) is described. Alkanethiols (RSH) were found to cause large synergi
stic shifts in the pH0.5 values for the extraction of cadmium (up to 2
.85 pH units for the addition of 0.25 M thiol to 0.25 M carboxylic aci
d), with much smaller shifts for zinc (up to 0.84 pH unit). With the i
someric C8-thiols, the extent of the shifts for both metals is greater
for the straight-chain compound (R = n-octyl) than for branched-chain
analogues (R = 2-ethylhexyl or 2-octyl). Smaller synergistic shifts w
ere obtained with dialkyl sulphides (RSR), whereas with dialkyl disulp
hides (RS.SR) slight antagonistic shifts were found. Slope analysis st
udies suggest that for mixtures of 3,5-diisopropylsalicylic acid (HA)
and 1-octanethiol (RSH), the extracted cadmium species has the stoichi
ometry CdA(HA)Cd4(RS)10CdA(HA), for which two possible structures are
suggested. With these extractant mixtures, the separation between the
pH0.5 values for cadmium and zinc is about one pH unit, and about two
pH units between cadmium and nickel for the extraction of 0.05 M metal
sulphates from 0.20 M sodium sulphate. However, the distribution coef
ficient at a given pH value decreases markedly with decreasing cadmium
concentration, making efficient recovery of metal values difficult.