过氧二硫酸盐
过硫酸盐
化学
羟基自由基
降级(电信)
核化学
纳米复合材料
硫酸盐
无机化学
零价铁
催化作用
环境化学
四溴双酚A
激进的
吸附
材料科学
纳米技术
有机化学
电信
阻燃剂
计算机科学
作者
Zhongting Rao,Nengwu Zhu,Xiaorong Wei,Fei Li,Pingxiao Wu,Zhi‐Min Dang,Bofan Cui
标识
DOI:10.1016/j.jhazmat.2021.126029
摘要
Peroxydisulfate (PDS) is a promising oxidant for sulfate radical based advanced oxidation processes (SAOPs), however its efficient activation is still a challenge. In this study, biochar-supported nano-zerovalent iron (nZVI) and copper oxide (CuO) nanocomposite (nZVI/[email protected]), derived from low-cost wastes including scrap iron filings, copper leaching solution and corn stalks, was successfully fabricated for PDS activation to enhance tetrabromobisphenol A (TBBPA) degradation in alkaline environment. Under the conditions of 100 mg/L nZVI/[email protected], 0.2 mM PDS, pH 8.0 and 25 °C, 86.32% of PDS was activated and 98.46% of TBBPA was degraded within 45 min in nZVI/[email protected] PDS system. When the PDS concentration was 2 mM, the nZVI/[email protected] PDS system realized efficient debromination and mineralization of TBBPA at the ratio of 79.12% and 79.36%, respectively. The results of EPR studies and radical scavenger experiments revealed that both hydroxyl radical (·OH) and sulfate radical (SO4·-) were responsible for TBBPA degradation. The nZVI could active PDS indirectly through electron transfer mechanism and exhibited synergistic effects with CuO on PDS activation. Furthermore, the nZVI/[email protected] PDS system showed good potential to degrade TBBPA in real water environment. Therefore, nZVI/[email protected] could be a novel strategy for efficient PDS activation and TBBPA degradation in alkaline environment.
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