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Mechanism for enhanced degradation of clofibric acid in aqueous by catalytic ozonation over MnOx/SBA-15

机译:MnOx / SBA-15催化臭氧化提高水溶液中氯纤维酸降解的机理

摘要

Comparative experiments were conducted to investigate the catalytic ability of MnOx/SBA-15 for the ozonation of clofibric acid (CA) and its reaction mechanism. Compared with ozonation alone, the degradation of CA was barely enhanced, while the removal of TOC was significantly improved by catalytic ozonation (O-3/MnOx/SBA-15). Adsorption of CA and its intermediates by MnOx/SBA-15 was proved unimportant in O-3/MnOx/SBA-15 due to the insignificant adsorption of CA and little TOC variation after ceasing ozone in stopped-flow experiment. The more remarkably inhibition effect of sodium bisulfite (NaHSO3) on the removal of TOC in catalytic ozonation than in ozonation alone elucidated that MnOx/SBA-15 facilitated the generation of hydroxyl radicals ((OH)-O-center dot), which was further verified by electron spin-resonance spectroscopy (ESR). Highly dispersed MnOx on SBA-15 were believed to be the main active component in MnOx/SBA-15. Some intermediates were indentified and different degradation routes of CA were proposed in both ozonation alone and catalytic ozonation. The amounts of small molecular carboxylic acids (i.e., formic acid (FA), acetic acid (AA) and oxalic acid (OA)) generated in catalytic ozonation were lower than in zonation alone, resulting from the generation of more (OH)-O-center dot. (C) 2014 Elsevier B.V. All rights reserved.
机译:进行了比较实验,以研究MnOx / SBA-15对氯纤维酸(CA)臭氧氧化的催化能力及其反应机理。与单独的臭氧化相比,CA的降解几乎没有增强,而催化臭氧化(O-3 / MnOx / SBA-15)显着改善了TOC的去除。在停止流实验中,由于CA的吸附微不足道且停止臭氧后TOC的变化很小,因此在O-3 / MnOx / SBA-15中,MnOx / SBA-15对CA及其中间体的吸附并不重要。亚硫酸氢钠(NaHSO3)在催化臭氧氧化中对TOC去除的抑制作用比仅在臭氧氧化中具有更显着的抑制作用,这表明MnOx / SBA-15促进了羟基自由基((OH)-O-中心点)的生成,这进一步通过电子自旋共振光谱(ESR)验证。 SBA-15上高度分散的MnOx被认为是MnOx / SBA-15中的主要活性成分。鉴定了一些中间体,并提出了单独臭氧化和催化臭氧化中CA的不同降解途径。催化臭氧化反应中生成的小分子羧酸(即甲酸(FA),乙酸(AA)和草酸(OA))的量低于单独的区域化,这是由于生成了更多(OH)-O -中心点。 (C)2014 Elsevier B.V.保留所有权利。

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