Chitosan is a unique biopolymer due to its cationic properties in acidic so
lutions. Protonation of the amino groups induces ion-exchange properties th
at can be used for anion recovery. As this sorbent is soluble in acidic med
ia, it may be necessary to reinforce its chemical stability using a glutara
ldehyde cross-linking treatment. Sorption properties are strongly influence
d by the pH of the solution and the presence of competitor anions, especial
ly sulfate anions. This competitor effect may be decreased by the grafting
of sulfur derivatives on the chitosan backbone using glutaraldehyde as a li
nker between the polysaccharide chains and the substituent. Several techniq
ues such as FTIR and SEM-EDAX were used for the chemical characterization o
f chitosan substitution and for the location of PGM sorption on the sorbent
. Sorption isotherms and kinetics were investigated and compared for cross-
linked materials and substituted polymers, and special attention was given
to the influence of competitor anions. The grafting of sulfur compounds inc
reased sorption capacities and decreased the competition of sulfate and chl
oride anions. While cross-linked materials sorbed platinum and palladium th
rough anion exchange, the grafting of sulfur moities gave chelating functio
nalities to the ion-exchange resin.