Nitrogen-doped carbon enhances Fe0 activation for efficient tetrabromobisphenol a decontamination and its removal mechanism

四溴双酚A 化学 零价铁 单线态氧 过氧化氢 废水 过氧二硫酸盐 人体净化 铁质 核化学 环境化学 氧气 催化作用 有机化学 吸附 废物管理 阻燃剂 工程类
作者
Lu Yang,Xiaoying Jin,Gary Owens,Zuliang Chen
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:482: 148839-148839 被引量:7
标识
DOI:10.1016/j.cej.2024.148839
摘要

Biomass derived N-doped carbon-encapsulated nano zero-valent iron (NC@Fe0) was successfully used to activate hydrogen peroxide (H2O2) for efficient oxidation of tetrabromobisphenol A (TBBPA). The as-prepared NC@Fe0 exhibited high H2O2 activation performance, with a TBBPA removal efficiency of 95.9 % and an oxidation rate constant of 0.031 min−1. The quenching experiments and electrochemical tests showed that the overall contributions of nonradical pathways were over 83.0 %, via synergistic production of singlet oxygen (1O2) and an electron transfer process (ETP). Specifically, the N group on NC@Fe0 greatly enhanced 1O2 production, while formation of surface complexes (OVs-H2O2) was responsible for the ETP mechanism. High Performance Liquid Chromatography Quadrupole Time-of-Flight Mass Spectrometer (HPLC-Q-TOF MS/MS) and Toxicity Estimation Software Tool (T.E.S.T) clearly demonstrated that products were mainly generated via debromination and β-scission, where the products were less toxic than the parent. During practical wastewater, in both lake water and domestic wastewaters, NC@Fe0/H2O2 removed over 91.0 % of TBBPA. This study highlighted the considerable contribution of nonradicals in contaminant removal and enriched our understandings of a green activator for future environmental remediations.
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