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Degradation of Aqueous Quinoline Using Persulfate Activated by γ-Fe2O3@Carbon Composites and Enhanced by UV Irradiation

机译:使用γ-FE2O3@碳复合材料激活并通过紫外线照射增强的过硫酸盐降解水喹啉

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摘要

In this study, the ultraviolet(UV)enhanced γ-Fe2O3@Carbon composite(γ-Fe2O3@C)persulfate(PS)activation system was successfully constructed for quinoline degradation. Quinoline can be effectively degraded with the removal efficiency of 99% and TOC removal efficiency of 86% in 60 min at pH 7.5 due to the increased contribution of SO4~(*·)and *OH caused by the assistance of UV irradiation in the γ-Fe2O3@C/PS system. Control experiments showed that the quinoline removal efficiency might be primarily restricted by the limited PS dosage and the system had a wide pH application range of 3~ 11, good tolerance and strong anti-interference ability. In the presence of the reactive oxygen species(SO4~(*·), ~·OH and ~1O_2),quinoline was first decomposed into formic acid, aniline, ethylbenzene and other intermediate products through hydroxylation, oxidative dehydrogenation and ring-opening reactions and then most of them were mineralized into carbon dioxide and water eventually.
机译:在这项研究中,紫外线(UV)增强的γ-FE2O3@碳复合材料(γ-FE2O3@c)perpulfate(PS)激活系统成功地用于喹啉降解。 由于SO4〜( *·)的贡献增加,在60分钟内,在60分钟内的99%的去除效率和TOC的去除效率在60分钟内可有效降解,而TOC的去除效率为86%,并且由γ辐照在γ辐射中的贡献增加,而 *OH。 -Fe2O3@C/PS系统。 对照实验表明,喹啉去除效率可能主要受到PS剂量有限的限制,并且该系统的pH施用范围为3〜11,良好的公差和强大的抗干扰能力。 在存在活性氧(SO4〜(*·),OH和〜1O_2)的情况下,首先将喹啉分解为甲酸,苯胺,乙烯苯和其他中间产物,通过羟基化,氧化脱水和环的反应和环反应和环反应以及环的反应以及环氧化反应以及环化反应以及环 然后,大多数人最终被矿化成二氧化碳和水。

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