Adsorption Behavior and Mechanism of Rhodamine B on a Polyvinyl Alcohol/Carboxymethyl Chitosan Hydrogel: Integrated Experimental and Computational Study

Shi Yi(Hunan Vocational Institute of Technology), Qingyun Li(Central South University of Forestry and Technology), Xinrui Zhu(Central South University of Forestry and Technology), Li S(Central South University of Forestry and Technology), Ting Hu(Central South University of Forestry and Technology), Xinyi Huang(Central South University of Forestry and Technology), J Y Luo(Central South University of Forestry and Technology), Hongbo Xiao(Central South University of Forestry and Technology), Yihui Zhou(Hunan Vocational Institute of Technology), B Wang(Nanchang Institute of Technology), Rongkui Su(Central South University of Forestry and Technology), Xiping Lei(Hunan Vocational Institute of Technology)
Molecules
May 11, 2026
Cited by 0Open Access
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Abstract

In this study, a polyvinyl alcohol/carboxymethyl chitosan (PVA/CCTS) hydrogel was synthesized via free radical polymerization and employed for the adsorption of Rhodamine B (RhB) from aqueous solution. The hydrogel was systematically characterized by FTIR, SEM, XPS, and BET analyses, confirming its interconnected porous network and functional group composition. Under optimized conditions (adsorbent dosage = 0.1 g, pH = 6, RhB concentration = 65 mg·L−1, and T = 298.15 ± 2 K), the maximum adsorption capacity reached 15.88 mg·g−1. Kinetic analysis showed that the pseudo-second-order model best described the adsorption behavior under optimal conditions, indicating that the uptake of RhB is governed by multiple interaction mechanisms rather than simple physisorption alone. The equilibrium data were best fitted by the Freundlich isotherm (R2 = 0.976), indicating surface heterogeneity of the hydrogel. Thermodynamic evaluation revealed an endothermic (ΔH = 28.38 ± 4.40 kJ·mol−1), with adsorption efficiency improving at elevated temperatures. The hydrogel retained appreciable adsorption capacity after three adsorption–desorption cycles (5.78 mg·g−1 at the third cycle). Density functional theory (DFT) calculations identified -COOH and -NH2 groups as the primary active sites, and molecular electrostatic potential analysis confirmed that electrostatic interactions between the negatively charged hydrogel surface and cationic RhB drive the initial adsorption. Molecular dynamics (MD) simulations over 100 ns further demonstrated that van der Waals forces constitute the dominant driving force, supplemented by electrostatic interactions and hydrogen bonding, with the hydrogel’s cross-linked network stabilizing adsorbed RhB molecules. The integrated experimental computational approach provides a comprehensive mechanistic understanding of RhB adsorption on PVA/CCTS hydrogel, offering guidance for the rational design of polysaccharide-based adsorbents for dye-contaminated wastewater treatment.


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