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熔融盐诱导氮掺杂生物炭纳米片作为高效过一硫酸盐催化剂用于有机污染物降解。

Molten salt induced nitrogen-doped biochar nanosheets as highly efficient peroxymonosulfate catalyst for organic pollutant degradation.

机构信息

Department of Pharmaceutical & Biological Engineering, School of Chemical Engineering, Sichuan University, Chengdu, 610065, PR China.

Department of Pharmaceutical & Biological Engineering, School of Chemical Engineering, Sichuan University, Chengdu, 610065, PR China.

出版信息

Environ Pollut. 2020 May;260:114053. doi: 10.1016/j.envpol.2020.114053. Epub 2020 Jan 23.

DOI:10.1016/j.envpol.2020.114053
PMID:31995772
Abstract

Advanced oxidation processes based on carbon catalysis is a promising strategy possessing great potential for environmental pollution degradation. Herein, nitrogen-doped biochar nanosheets (NCS-x) were synthesized using a nitrogen-rich biomass (Candida utilis) as sole precursor. The involvement of environmental-friendly molten salt (NaCl and KCl) in pyrolysis process not only facilitated the exfoliation of biochar, but also favored the retention of N element in biochar. When applying as catalyst for peroxymonosulfate activation, the as-obtained NCS-6 exhibited outstanding performance in catalytic degradation of bisphenol A (BPA). A 100% removal efficiency was observed in 6 min with fast reaction kinetic (k = 1.36 min). Based on quenching test and in-situ electron paramagnetic resonance analysis, both radical pathway and non-radical pathway were suggested to be involved in BPA degradation, while singlet oxygen was identified as the dominant reactive oxygen species. Furthermore, the ecotoxicity evaluation using Chlorella vulgaris as ecological indicator indicated that BPA solution after degradation was less toxic than the original solution. It is expected that this green and facile strategy holds great promise for value-added conversion of nitrogen-rich biomass to highly efficient biochar nanosheets for environment remediation.

摘要

基于碳催化的高级氧化工艺是一种很有前途的环境污染降解策略,具有巨大的潜力。本文采用富氮生物质(Candida utilis)为唯一前驱体,合成了氮掺杂生物炭纳米片(NCS-x)。环境友好型熔盐(NaCl 和 KCl)在热解过程中的参与不仅促进了生物炭的剥离,而且有利于 N 元素在生物炭中的保留。将所得到的 NCS-6 作为过一硫酸盐(PMS)的活化催化剂,在催化降解双酚 A(BPA)时表现出优异的性能。在 6 分钟内即可达到 100%的去除效率,反应动力学较快(k=1.36 min)。通过猝灭实验和原位电子顺磁共振分析,推测 BPA 的降解涉及自由基途径和非自由基途径,而过氧化氢是主要的活性氧物种。此外,以小球藻(Chlorella vulgaris)为生态指标进行的生态毒性评价表明,降解后的 BPA 溶液的毒性比原始溶液低。预计这种绿色简便的策略为富氮生物质向高效生物炭纳米片的增值转化,用于环境修复提供了广阔的前景。

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