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Algal Surface-Inspired Chitosan-Modified Monodisperse Porous Polystyrene Microspheres: Pore Size Regulation and Adsorption Mechanism for Biopharmaceutical Wastewater

吸附 分散性 生物制药 化学工程 聚苯乙烯 壳聚糖 废水 微球 多孔性 机制(生物学) 化学 材料科学 纳米技术 色谱法 有机化学 聚合物 环境科学 环境工程 哲学 认识论 生物 工程类 遗传学
作者
Xiangchi Liu,Haowei Shen,Ailing Liu,Jie Hou,Yafang Cheng,Xinyu Yao,Haomiao Yang,Baijun Liu,Mingyao Zhang
出处
期刊:Langmuir [American Chemical Society]
卷期号:41 (32): 21745-21756
标识
DOI:10.1021/acs.langmuir.5c02753
摘要

Monodisperse porous polystyrene microspheres (PPS) and their derivatives were successfully fabricated via a two-step swelling polymerization approach combined with secondary cross-linking technology. Inspired by the surface morphology of algae, PPS and derivatives were subsequently modified using chitosan with different viscosities (CS-1 and CS-2), thereby constructing chitosan-functionalized PPS. By precisely adjusting the amounts of vinyl chloroacetate (VCA) and the cross-linker 1,4-bis(chloromethyl)benzene (XDC), the pore size of PPS and derivatives could be finely tuned within the range of 5-20 nm. The specific surface area of PPS after secondary cross-linking (HPPS) reached up to 380.79 m2/g, which is approximately 3-5 times higher than that of uncross-linked PPS. Surface modification with chitosan significantly enhanced the water dispersibility, suspension stability, and adsorption capacity of PPS and derivatives toward organic pollutants. The adsorption kinetics of the modified microspheres were better described by a pseudo-second-order model. Notably, PPS containing chlorinated groups and modified with CS-2 (PPS-Cl@CS-2) retained over 80% of their adsorption efficiency after five consecutive cycles. This study presents a viable strategy for constructing porous microspheres with tunable structures and synergistically optimized performance, offering a practical pathway for the regulation of pore size and functional surface modification in porous materials.
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