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
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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