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Insights into the synergy of zero-valent iron and copper oxide in persulfate oxidation of Orange G solutions

机译:深入了解Orange G溶液过硫酸盐氧化中零价铁和氧化铜的协同作用

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摘要

The degradation of Orange G (OG) by persulfate (PS, S2O8 (2-)) activated with dual catalysts that combined zero-valent iron (ZVI) and copper oxide (CuO) was investigated through batch experiments. Effects of pH, initial OG concentration, persulfate dosages, and dosages of dual catalysts on OG degradation were also examined. Higher persulfate concentration and catalysts dosages resulted in higher OG degrading rates. The OG degradation was higher under acidic conditions (pH 3.0 and 5.0) when compared to alkaline conditions. The constituents and the morphology of the catalysts coating before and after reaction were also investigated with X-ray diffraction and scanning electron microscopy. Radical mechanism was studied and three radical scavengers [methanol (MA), tert-butanol (TBA), phenol] were used to determine the type of major active species taking part in the degradation of OG. It was assumed that the or played a major role in the OG degradation. In conclusion, the ZVI/CuO/PS system is a good candidate for use in detoxifying water contaminants.
机译:通过分批实验研究了过硫酸盐(PS,S2O8(2-))在零价铁(ZVI)和氧化铜(CuO)结合的双重催化剂的作用下对橙G(OG)的降解作用。还检查了pH,初始OG浓度,过硫酸盐剂量和双重催化剂剂量对OG降解的影响。较高的过硫酸盐浓度和催化剂用量导致较高的OG降解速率。与碱性条件相比,在酸性条件下(pH 3.0和5.0),OG降解更高。还通过X射线衍射和扫描电子显微镜研究了反应前后催化剂涂层的组成和形态。研究了自由基机理,并使用三种自由基清除剂[甲醇(MA),叔丁醇(TBA),苯酚]确定参与OG降解的主要活性物质的类型。假定或在OG降解中起主要作用。总之,ZVI / CuO / PS系统是用于对水污染物进行解毒的理想选择。

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