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Mechanism of heterogeneous activation of persulfate with FeOCl under visible light irradiation

机译:FeOCl在可见光照射下过硫酸盐的非均相活化机理

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摘要

Activation of persulfate (PS) by ultraviolet light or transition metal catalysts has been extensively studied. However, little is known about the activation of PS by iron oxychloride (FeOCl) in the presence of visible light irradiation. Herein, the catalytic activity of FeOCl was developed for oxidative degradation of rhodamine B (RhB) with the FeOCl/PS/Vis process. The characterization of FeOCl for reaction kinetics, degradation mechanism, and catalyst stability was investigated. It is found that the redox cycle of iron species and photoinduced electrons formed on the FeOCl catalyst surface can effectively activate PS, to generate radicals. Based on quenching experiments and electron paramagnetic resonance, the photogenerated holes (h(+) ) and sulfate radicals (SO4-center dot) are the predominant reactive oxidants for RhB decolorization, while superoxide radicals (center dot O-2(-)) and hydroxyl radicals (center dot OH) are also involved. Moreover, FeOCl shows good catalytic performance in a wide range of pH values (pH = 3-10) and excellent reusability and stability, as well.
机译:已经对紫外线或过渡金属催化剂对过硫酸盐(PS)的活化进行了广泛的研究。但是,关于在可见光照射下氧氯化铁(FeOCl)对PS的激活知之甚少。在此,利用FeOCl / PS / Vis方法开发了FeOCl的催化活性,用于罗丹明B(RhB)的氧化降解。研究了FeOCl的反应动力学,降解机理和催化剂稳定性。发现铁物种的氧化还原循环和在FeOCl催化剂表面上形成的光致电子可以有效活化PS,产生自由基。基于淬灭实验和电子顺磁共振,光生空穴(h(+))和硫酸根(SO4-中心点)是RhB脱色的主要活性氧化剂,而超氧自由基(中心点O-2(-))和还涉及羟基自由基(中心点OH)。而且,FeOCl在很宽的pH值范围(pH = 3-10)中显示出良好的催化性能,并且还具有出色的可重复使用性和稳定性。

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