苯胺
吸附
聚苯乙烯
介孔材料
聚合物
化学
大孔隙
烷基化
高分子化学
化学工程
多孔性
材料科学
有机化学
催化作用
工程类
作者
You Wang,Ziming Liang,Yiwen Cao,Shiyuan Wei,Xiaomei Wang,Fa Zhou,Jianhan Huang
标识
DOI:10.1021/acs.iecr.4c01923
摘要
Herein, both surface chemistry engineering and pore partition strategies were adopted to regulate the pore environments of the hyper-crosslinked polymers (HCPs) to strengthen their aniline adsorption from water. Specifically, plentiful carboxyl groups were first anchored on the macropores of polystyrene through the nucleophilic substitution, and then abundant rigid methylene partitioned the macropores of polystyrene into abundant micropores/mesopores through the Friedel–Crafts alkylation. As a result, carboxyl-functionalized HCPs were accurately prepared as planned. PS-BTCA-HCP-4 exhibited the highest adsorption to aniline, boasting the qmax of 396 mg/g, which can be largely attributed to its highest SBET of 478.0 m2/g and the rich carboxyl groups with the oxygen content of 11.31%. Furthermore, it achieved adsorption equilibrium within 70 min, and its deliberately hierarchical porosity consisting of plentiful micropores/mesopores made a positive contribution.
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