过氧二硫酸盐
生物炭
过硫酸盐
化学
激进的
零价铁
降级(电信)
催化作用
光化学
兴奋剂
无机化学
热解
材料科学
有机化学
吸附
电信
光电子学
计算机科学
作者
Jiaqi Li,Qintie Lin,Haoyu Luo,Hengyi Fu,Libin Wu,Yijun Chen,Yongjie Ma
标识
DOI:10.1016/j.jwpe.2022.102681
摘要
To gain a deeper understanding of the roles of N-doping in nanoscale zero-valent iron (nZVI)-based catalysts for persulfate-based advanced oxidation processes (AOPs), five catalysts, biochar (BC), N-doped biochar (NBC), nZVI, nZVI-loaded pristine biochar ([email protected]) and nZVI-loaded N-doped biochar ([email protected]), were prepared for peroxydisulfate (PDS) activation to degrade bisphenol A (BPA). Because of the synergy between nZVI and NBC, [email protected] exhibited a better catalytic ability and possessed more active species in PDS activation. Mechanisms were proposed including radical pathways (HO• and SO4•−) and nonradical pathways (1O2). PDS activation by Fe0 generated radicals while graphitic N, pyridinic N and CO in [email protected] were employed for 1O2 generation. In addition, [email protected] showed a high anti-interference capacity and stability. The analysis of the intermediates produced by the degradation of BPA confirmed that HO•, SO4•− and 1O2 are involved in the reaction of the [email protected] system. Our research provides a new perspective on the synergistic effect of nZVI and N-doped materials in AOPs for endocrine disrupter degradation.
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