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摘要:
Diatomite supported nano zero valent iron (nZVI) catalyst (NDA) with complex network structure was prepared via a mild reduction precipitation method in this work.The pore structure and pore distribu-tion of NDA can be regulated and controlled through adjusting the loading amount of nZVI.In general,the nano three-dimensional network formed by nZVI and diatomite channels greatly increase the specific surface area and pore volume of NDA,and further formed more active sites,which made NDA have better performance in activating PMS to degrade BPA than pure nZVI.The pseudo-first-order reaction rate con-stant of 50-NDA (50%-nZVI/diatomite) is almost 3 times higher than that of pure nZVI.Besides,the elec-tron paramagnetic resonance (EPR) and radical quenching experiments showed that the activation process was dominated by the sulfate radical (SO4·-) and hydroxyl radical (OH) produced by Fe0 oxidation.The generated electrons promote the self-decomposition of PMS to produce singlet oxygen (1O2),and then the valence state of iron changes to produce free radicals.In addition,the possible degradation pathway of BPA was inferred from the intermediate products identified by liquid chromatograph-mass spectrom-eter (LC-MS).This study provides a novel strategy for the design and preparation of three-dimensional composite catalysts derived from natural mineral.
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篇名 Diatomite supported nano zero valent iron with 3D network for peroxymonosulfate activation in efficient degradation of bisphenol A
来源期刊 材料科学技术(英文版) 学科
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年,卷(期) 2021,(36) 所属期刊栏目
研究方向 页码范围 57-69
页数 13页 分类号
字数 语种 英文
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材料科学技术(英文版)
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1005-0302
21-1315/TG
大16开
沈阳市沈河区文化路72号
1985
eng
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