过氧二硫酸盐
生物炭
电子转移
硼
化学
催化作用
碳纤维
化学工程
电化学
猝灭(荧光)
光化学
材料科学
无机化学
有机化学
荧光
物理化学
电极
复合材料
复合数
物理
工程类
量子力学
热解
作者
Banghai Liu,Wanqian Guo,Huazhe Wang,Qishi Si,Qi Zhao,Haichao Luo,Nanqi Ren
标识
DOI:10.1016/j.cej.2020.125119
摘要
In this study, B-doped graphitic porous biochar (B-KBC) was prepared and used to activate peroxydisulfate (PDS) for the removal of sulfamethoxazole (SMX). Experimental and theoretical results revealed that the introduction of boron species not only act as Lewis acid sites enhanced the surface affinity towards PDS but also modulate the electronic structure of carbon matrix evidently increase the electron transfer rate, and thus result in an excellent catalytic capacity. More importantly, owing to the high stability boron sites, B-KBC endows a superior long-term durability in comparison with popular N-doped carbon catalysts. Given the uncertainty of quenching experiments, the electron paramagnetic resonance, materials balance calculation combined with electrochemical measures confirmed the biochar mediated electron transfer mechanism, rather than 1O2, was primarily responsible for the nonradical route. This study is expected to pave a new avenue to develop cost-effective and eco-friendliness metal-free carbon catalyst with adequate activity and reuse stability.
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