Preparation and Characterization of SA / GO / PEG Gel Beads and Their Adsorption Properties for Pb 2+

吸附 聚乙二醇 化学工程 材料科学 结晶度 热稳定性 朗缪尔吸附模型 有孔小珠 聚合 聚乙烯 乙二醇 石墨烯 PEG比率 表征(材料科学) 聚合物 硅胶 氧化物 聚合度 原材料 色谱法 微乳液 化学 环氧乙烷 环境污染 蛋白质吸附 海藻酸钠 热分析 高分子化学
作者
Xiaofang You,Yuxia Hou,Jingwei Wang,Lin Li,Meng He
出处
期刊:Journal of Applied Polymer Science [Wiley]
卷期号:143 (12)
标识
DOI:10.1002/app.70338
摘要

ABSTRACT This study aims to address the challenge of treating Pb 2+ in mining wastewater, a persistent issue in water environment pollution control. The sodium alginate/graphene oxide/polyethylene glycol (SA/GO/PEG) gel beads were designed and prepared with graphene oxide (GO), sodium alginate (SA), and polyethylene glycol (PEG) as raw materials by combining experiments and simulation. Firstly, the simulation system of SA/GO/PEG gel bead was constructed through molecular simulation, and the optimal composition of SA/GO/PEG gel bead was determined. The simulation results indicated that, with a PEG polymerization degree of 4000, the SA/GO/PEG gel bead system exhibited the greatest structural stability and the most effective cross‐linked. Based on the understanding of the structure–performance relationship, SA/GO/PEG4000 gel beads were prepared to achieve an adsorbent with both high adsorption capacity and good stability. Characterization results indicated the successful cross‐linked of polyethylene glycol with sodium alginate and graphene oxide, which not only introduced additional oxygen‐containing functional groups and increased the crystallinity of the gel beads but, more importantly, led to the formation of a dense and complex three‐dimensional network. This structure contributed to the improved thermal stability of the composite. Adsorption experiments showed that the adsorption of Pb 2+ onto SA/GO/PEG gel beads followed the Langmuir isotherm model. The calculated maximum adsorption capacities at 25°C, 35°C, and 45°C were 490.20, 497.51, and 526.32 mg/g, respectively. Furthermore, the gel beads exhibited excellent reusability, retaining 92.64% of their initial adsorption capacity after four consecutive adsorption–desorption cycles.
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