Abstract
Based on the premise that aqueous anions of hexavalent chromium (Cr(VI)) are capable of electrostatic interaction with cationic and polar active sites, acid-washed Madacamia nutshell biomass was sequentially treated with diethylenetriamine (DETA) and maleic anhydride (MA) to graft poly(diethylenetriamine–co–maleic anhydride). By displaying a new peak at 1685 cm−1 ascribed to amide CO stretching vibrations, Fourier transform infrared spectroscopy highlighted the formation of amide groups through reaction of DETA with carboxyl groups on the biomass surface. Scanning electron microscopic images of the MA-modified biomass displayed polymeric growths attributed to copolymerization of DETA with MA. The polar and ionizable amide and amine groups of the grafted copolymer endowed the adsorbent with Cr(VI) removal capabilities over a wide pH range demonstrated by removal efficiencies between 70.9% and 81.7% in the pH 1.6 to pH 10.0 range for the treatment of 20 mL solutions containing 100 mg L−1 Cr(VI) with 200 mg of adsorbent. Conformity of the adsorption isotherm data to the Freundlich model revealed the heterogeneous nature of the adsorbent surface, which comprised a variety of functional groups capable of interaction with Cr(VI) species in solution. The Sips isotherm model provided the best fit to the equilibrium experimental data, and the adsorption capacity was 779.1 mg g−1 at pH 1.6, room temperature and an adsorbent dosage of 5.0 g L−1. The findings indicate that Cr(VI) adsorption onto diethylenetriamine and maleic anhydride modified Madacamia nutshell biomass is a promising option for Cr(VI) removal from aqueous solutions.
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