吸附
双酚A
微型多孔材料
化学
三嗪
化学工程
双酚
氮气
聚合物
多孔性
有机化学
工程类
环氧树脂
作者
Xuechun Yang,Xiaoyi Zhang,Xinwei Chen,Xiaoying Gao,Yunjia Liu,Jinlan Weng,Shenghong Yang,Tian Gui,Xiangshu Chen,Ru‐Song Zhao,Jian Liu
出处
期刊:Chemosphere
[Elsevier BV]
日期:2022-08-08
卷期号:307: 135919-135919
被引量:5
标识
DOI:10.1016/j.chemosphere.2022.135919
摘要
Achieving both rapid adsorption rate and high adsorption capacity for bisphenol micropollutants from aquatic systems is critical for efficient adsorbents in water remediation. Here, we elaborately prepared three nitrogen-rich triazine-based porous polymers (NTPs) with similar geometric configurations and nitrogen contents (41.70-44.18 wt%) while tunable BET surface areas and micropore volumes in the range of 454.7-536.3 m2 g-1 and 0.20-0.84 cm3 g-1, respectively. It was systematically revealed that the synergy of hydrogen bonding, π-π electron-donor-acceptor interaction, and micropore preservation promoted the rapid (within 5 min) and high capacity adsorption of bisphenols by NTPs. Particularly, microporous-dominated NTPs-3 with the highest micro-pore volume (0.84 cm3 g-1) displays remarkable adsorption capacity towards bisphenol A as evidenced by the adsorption capacity of 182.23 mg g-1. A simple column filter constructed by NTPs-3 also expressed good dynamic adsorption and regeneration capacity. This work provided new insight into the rational design and engineering of nitrogen-rich porous polymers for the remediation of micropollutant wastewater.
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