Heterogeneous catalysis of ozone using ordered mesoporous Fe3O4 for degradation of atrazine

催化作用 介孔材料 X射线光电子能谱 浸出(土壤学) 化学 傅里叶变换红外光谱 化学工程 降级(电信) 吸附 多相催化 臭氧 核化学 有机化学 电信 计算机科学 工程类 土壤科学 土壤水分 环境科学
作者
Shumin Zhu,Bingzhi Dong,Yanghai Yu,Lingjun Bu,Jing Deng,Shiqing Zhou
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:328: 527-535 被引量:139
标识
DOI:10.1016/j.cej.2017.07.083
摘要

Ordered mesoporous Fe3O4 catalyst was successfully fabricated using KIT-6 as the hard template through a nanocasting route and innovatively investigated as a heterogeneous ozonation catalyst. The morphology and physico-chemical properties of as-prepared catalysts were characterized by X-way diffraction, Fourier transform infrared, transmission electron microscopy, X-ray photoelectron spectroscopy and N2 adsorption-desorption techniques. Results showed that the surface area and average pore size of mesoporous Fe3O4 were 154.2 m2 g−1 and 6.2 nm, respectively. The mesoporous Fe3O4 catalyst presented superior catalytic activity for removing atrazine (ATZ) during ozonation compared to conventional Fe3O4 nanoparticles. The contribution of homogeneous ozonation reaction catalyzed by leaching irons was negligible, suggesting that the degradation of ATZ was mainly dominated by heterogeneous reaction catalyzed by mesoporous Fe3O4. Moreover, the removal rate of ATZ increased with the increase of catalyst dosage and solution pH. Based on the results of XPS analysis and radical scavenging test, a plausible mechanism was proposed. The redox cycles of Fe2+/Fe3+ was responsible for hydroxyl radical (OH) generation and OH dominantly contributed to the degradation of ATZ in this study. Finally, the possible transformation pathways of ATZ degradation were proposed and the toxicity of degradation products was evaluated. The results demonstrated that ordered mesoporous Fe3O4 is a promising catalyst for ozonation process, especially treating water polluted by ozone-resistant contaminants.
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