RESUMO
Bone char powder, composed mainly of poorly crystalline hydroxyapatite (Ca(10)(PO(4))(6)(OH)(2)), carbon and CaCO(3), has potential applicability in the removal of Co(2+) ions from contaminated effluents. In the present study, the influence of process parameters: particle size, agitation speed, initial pH and initial sorbate concentration, onto kinetics and mechanism of Co(2+)sorption was studied and discussed. In order to describe and compare time evolution of the process under different conditions, the experimental data were analyzed using pseudo-first, pseudo-second and Vermeulen's kinetic models. Generally, experimental results were best fitted with the pseudo-second-order model, which accurately predicted the equilibrium sorbed amounts. The pseudo-second-order rate constant was the most influenced by variations in initial metal concentration and pH, in the investigated ranges. The conclusions about sorption mechanism were derived based on Co(2+) amounts sorbed during time, as well as considering solution pH changes, changes of Ca(2+) amounts released into liquid phase and Ca(2+)/Co(2+) molar ratios. It was concluded that rapid sorption stage was governed by surface complexation reactions, whereas the contribution of the ion-exchange mechanism increased with time and became more significant in the second, slower phase. Experimentally determined maximum sorption capacity towards Co(2+), under optimal conditions, was found to be 0.38 mmol/g. The results show that bone char represents cost-effective alternative to synthetic hydroxyapatite sorbent.
