Lignin/PVA hydrogel with enhanced structural stability for cationic dye removal

乙烯醇 结晶紫 阳离子聚合 吸附 朗缪尔吸附模型 木质素 化学工程 亚甲蓝 化学 高分子化学 聚乙烯醇 材料科学 聚合物 有机化学 催化作用 光催化 医学 病理 工程类
作者
Seungoh Jung,Heecheol Yun,Jungkyu Kim,Jong-Hwa Kim,Hwanmyeong Yeo,In-Gyu Choi,Hyo Won Kwak
出处
期刊:International Journal of Biological Macromolecules [Elsevier]
卷期号:257: 128810-128810 被引量:12
标识
DOI:10.1016/j.ijbiomac.2023.128810
摘要

In this study, a lignin-based hydrogel for wastewater treatment was prepared by incorporating kraft lignin (KL) into a poly (vinyl alcohol) (PVA) matrix. The underwater structural stability of the KL-PVA hydrogel was guaranteed through physicochemical crosslinking, involving freeze–thaw process and chemical crosslinking reaction. The KL-PVA hydrogel displayed superior compressive characteristics compared to the original PVA hydrogel. This improvement was attributed to the chemical crosslinking and the reinforcing effect of the incorporated KL microparticles. The incorporation of anionic KL microparticles into the PVA three-dimensional network structure enhanced the cationic methylene blue (MB) and crystal violet (CV) adsorption efficiency of the prepared KL-PVA hydrogel. The MB adsorption results were well explained by pseudo-2nd order kinetics model and Langmuir isotherm model. Electrostatic forces, hydrogen bonding and π-π stacking interactions were the main adsorption mechanisms between cationic dyes and KL surfaces, indicating the potential of KL-PVA hydrogel as an effective adsorption material. Moreover, regulating the molecular weight of PVA not only prevented lignin leakage from the KL-PVA hydrogel but also elevated the KL content within the hydrogel, consequently improving its dye removal performance. For KL-PVA hydrogel with high molecular weight PVA, the MB and CV adsorption capacities were 193.8 mg/g and 190.0 mg/g, respectively.
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