Abstract

Wool, a naturally occurring biopolymer made up of amino acids, is employed as an adsorbent for both modified and unmodified forms of the dyes rhodamine6G (R6G) and Cr6+. The two-step procedure of (i) ring opening polymerization (ROP) and (ii) condensation reaction was used to modify the structure of wool fibre. Both the ROP and the condensation provide steric free chain expanding groups as well as adsorption-improving groups. The FT-IR spectrum, which showed peaks about 1725 and 1630 cm−1 corresponding to the CO and CN stretchings, respectively, confirmed the structural modification. By detecting a slight hump at 8.5 ppm, 1H NMR was able to validate the later functional group. DSC, TGA, FE-SEM, EDX, and water contact angle (WCA) were also used to characterize it. With the aid of a UV–visible spectrophotometer, the quantitative adsorption of both Cr6+ and R6G by modified and unmodified Wool fibre was monitored. For the adsorption of Cr6+ and R6G, the pseudo first order and pseudo second order kinetics were used. The multilayer coating of adsorbate onto adsorbent was confirmed by the Langmuir adsorption isotherm. Thermodynamic parameters were calculated and compared to values found in the literature.

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