Enhancing the metal ion binding characteristics and reversal of selectivity of crosslinked chitosan sorbents through functionalisation for targeted applications

In this study, we report optimised synthesis of N-carboxymethylated chitosan (CM-Cts) and its crosslinking to obtain, for the first time, glutaraldehyde crosslinked N-carboxymethylated chitosan (CM-Cts-Glu) as a metal ion sorbent. CM-Cts and CM-Cts-Glu were characterised using FTIR and solid state 13C NMR techniques. As compared to epichlorohydrin, glutaraldehyde was found to be better suited for efficient synthesis of the crosslinked functionalised sorbent. CM-Cts-Glu showed better metal ion uptake properties compared to the crosslinked chitosan (Cts-Glu). Metal ion removal by CM-Cts-Glu was studied in detail under different conditions such as different initial solution concentrations, pH, presence of complexants and competing ions. Further, sorption-desorption kinetics was studied and it was shown that complete desorption and multiple cycles of reuse without any loss in capacity was feasible. The maximum Co(II) uptake obtained for CM-Cts-Glu was found to be 265 μmol/g, while for Cts-Glu it was 10 μmol/g. Metal ion sorption by CM-Cts-Glu was found to be through chelation by the carboxylic acid functional groups present over the chitosan backbone. Utility of the CM-Cts-Glu under complexing decontamination formulations used in nuclear industry was ascertained. While Cts-Glu generally preferred iron over cobalt under complexing conditions, it was shown that the selectivity was reversed in favour of Co(II) in the functionalised sorbent, CM-Cts-Glu. N-carboxylation followed by crosslinking with glutaraldehyde was found to be a feasible approach for the generation of superior chitosan-based sorbents.