催化作用
煅烧
钴
X射线光电子能谱
材料科学
无机化学
氮化物
甲基橙
氧化物
氧化钴
化学工程
化学
光催化
冶金
纳米技术
图层(电子)
生物化学
工程类
作者
K. S. Zhu,Changzi Jin,Z. Klencsár,Ganeshraja Ayyakannu Sundaram,Junhu Wang
出处
期刊:Catalysts
[MDPI AG]
日期:2017-05-04
卷期号:7 (5): 138-138
被引量:61
摘要
In meeting the need for environmental remediation in wastewater treatment and the development of popular sulfate-radical-based advanced oxidation processes (SR-AOPs), a series of Co/Fe-based catalysts with confirmed phase structure were prepared through extended soft chemical solution processes followed by atmosphere-dependent calcination. Powder X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and 57Fe Mössbauer spectroscopy were employed to characterize the composition, morphology, crystal structure and chemical state of the prepared catalysts. It was shown that calcination in air, nitrogen and ammonia atmospheres generated Co-Fe catalysts with cobalt ferrite (CoFe2O4), Co-Fe alloy and Co-Fe nitride as dominant phases, respectively. The prepared Co/Fe-based catalysts were demonstrated to be highly efficient in activating peroxymonosulfate (PMS) for organic Orange II degradation. The activation efficiency of the different catalysts was found to increase in the order CoFe2O4 < Co-Fe nitride < Co-Fe alloy. Sulfate radical was found to be the primary active intermediate species contributing to the dye degradation for all the participating catalysts. Furthermore, a possible reaction mechanism was proposed for each of the studied catalysts. This study achieves progress in efficient cobalt-iron catalysts using in the field of SR-AOPs, with potential applications in environment remediation.
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