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利用源自废物的 nZVI/CuO@BC 纳米复合材料高效活化过二硫酸盐,在碱性环境下降解四溴双酚 A。

Efficient peroxydisulfate activation with nZVI/CuO@BC nanocomposite derived from wastes for degradation of tetrabromobisphenol A in alkaline environment.

机构信息

School of Environment and Energy, South China University of Technology, Guangzhou 510006, PR China.

School of Environment and Energy, South China University of Technology, Guangzhou 510006, PR China; The Key Lab of Pollution Control and Ecosystem Restoration in Industry Cluster, Ministry of Education, Guangzhou 510006, PR China; Guangdong Provincial Key Laboratory of Solid Wastes Pollution Control and Recycling, Guangzhou 510006, PR China; Guangdong Environmental Protection Key Laboratory of Solid Waste Treatment and Recycling, Guangzhou 510006, PR China.

出版信息

J Hazard Mater. 2021 Sep 5;417:126029. doi: 10.1016/j.jhazmat.2021.126029. Epub 2021 May 5.

Abstract

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/CuO@BC), 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/CuO@BC, 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/CuO@BC-activated PDS system. When the PDS concentration was 2 mM, the nZVI/CuO@BC-activated 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 (SO) 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/CuO@BC-activated PDS system showed good potential to degrade TBBPA in real water environment. Therefore, nZVI/CuO@BC could be a novel strategy for efficient PDS activation and TBBPA degradation in alkaline environment.

摘要

过二硫酸盐(PDS)是一种很有前途的基于硫酸根自由基的高级氧化工艺(SAOPs)氧化剂,但其有效激活仍然是一个挑战。在本研究中,以包括废铁粉、铜浸出液和玉米秸秆在内的低成本废物为原料,成功制备了生物炭负载纳米零价铁(nZVI)和氧化铜(CuO)纳米复合材料(nZVI/CuO@BC),用于 PDS 活化以增强碱性环境中四溴双酚 A(TBBPA)的降解。在 100mg/L nZVI/CuO@BC、0.2mM PDS、pH 8.0 和 25°C 的条件下,86.32%的 PDS 被激活,在 nZVI/CuO@BC 活化过二硫酸盐系统中 45min 内 TBBPA 的降解率达到 98.46%。当 PDS 浓度为 2mM 时,nZVI/CuO@BC 活化过二硫酸盐系统实现了 TBBPA 的有效脱溴和矿化,脱溴率和矿化率分别为 79.12%和 79.36%。EPR 研究和自由基清除剂实验的结果表明,·OH 和 SO均参与了 TBBPA 的降解。nZVI 可以通过电子转移机制间接激活 PDS,并与 CuO 对 PDS 的激活表现出协同作用。此外,nZVI/CuO@BC 活化过二硫酸盐系统在实际水环境中具有良好的降解 TBBPA 的潜力。因此,nZVI/CuO@BC 可以作为一种在碱性环境中有效激活 PDS 和降解 TBBPA 的新策略。

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