Solvent Extraction Equilibrium in the CuSO4–H2SO4–LIX 984–ESCAID 103 System
Abstract
A previously determined thermodynamic model for extraction equilibrium is used as a basis to predict experimentally measured distribution coefficients for the CuSO4–H2SO4–LIX 984–Escaid 103 solvent extraction system at 25°C and aqueous copper concentrations in the range 0.01–2.0 g L–1, the copper loading isotherm is also obtained.