Biomass-derived N/S dual-doped hierarchically porous carbon material as effective adsorbent for the removal of bisphenol F and bisphenol S

杂原子 吸附 双酚A 碳纤维 密度泛函理论 化学工程 兴奋剂 生物量(生态学) 化学 打赌理论 多孔性 氢键 材料科学 有机化学 双酚 分子 复合材料 环氧树脂 计算化学 复合数 戒指(化学) 工程类 地质学 海洋学 光电子学
作者
Tao Wang,Jinhua Shen,Lewen Zheng,Shaopan Bao,Wen-Jun Li,Tao Fang,Baoshan Xing
出处
期刊:Journal of Hazardous Materials [Elsevier BV]
卷期号:416: 126126-126126 被引量:23
标识
DOI:10.1016/j.jhazmat.2021.126126
摘要

Biomass-derived heteroatom-doped porous carbon-based materials are emerging as low-cost adsorbents for removing common pollutants, although the adsorption performance is still unsatisfactory and the main adsorption mechanisms are still controversial. Herein, we report a facile and general method for fabricating biomass-derived N/S dual-doped hierarchically porous carbon adsorbent (MZ-NSPC). The MZ-NSPC material exhibits excellent adsorption capacity (295.8 mg/g for bisphenol F (BPF), 308.7 mg/g for bisphenol S (BPS)), short equilibrium time (30 min), and good reusability (the decline efficiency < 6.15% after five times). The remarkable adsorption performance originates from a large BET surface area, hierarchically porous structure, and N/S heteroatoms dual-doping. Combined with comparative experiments and density functional theory (DFT) calculations, we revealed that the doped N, S heteroatoms played a synergistic effect which promoted the adsorption performance and adsorption sites are mainly the oxidized-S and pyridinic-N. Importantly, for BPF, the proportion contribution of different mechanisms followed the order of hydrophobic interaction > π-π interaction > hydrogen bonding interaction. However, adsorption mechanism of BPS was mainly controlled by π-π interaction. This work not only promotes the development of low-cost and sustainable heteroatom-doped carbon-based materials, but also systematically studies adsorption mechanism of heteroatom-doped carbon-based materials for bisphenols.
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