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过氧乙酸活化二氯芬酸降解性能研究。

Degradation of diclofenac by Fe(II)-activated peracetic acid.

机构信息

Faculty of Geosciences and Environmental Engineering, Southwest Jiaotong University, Chengdu, People's Republic of China.

出版信息

Environ Technol. 2021 Nov;42(27):4333-4341. doi: 10.1080/09593330.2020.1756926. Epub 2020 Apr 30.

Abstract

In this study, peracetic acid (PAA) activated by Fe(II) was proposed to remove diclofenac (DCF) in polluted water. It was found that Fe(II)/PAA system could effectively remove DCF at neutral condition, which has a significant advantage over classical Fenton process. According to the result of scavenging experiment, both hydroxyl radical and peroxy radical were considered to be responsible for the degradation of DCF. The influence of several operational parameters including initial pH, Fe(II) dosage, PAA concentration and common water matrix on DCF removal were investigated. 80% DCF was removed at mild condition (pH 6-7) within 60 s, and its removal rate could be enhanced with the increase in Fe(II) dosage and PAA concentration. Presence of and natural organic matter (NOM) was proved to have a significantly negative impact on DCF degradation. Four probable degradation pathways of DCF were proposed based on the detected reaction products, including hydroxylation, C-N bond cleavage, decarboxylation and dehydrogenation.

摘要

在这项研究中,提出了用 Fe(II) 激活过氧乙酸(PAA)来去除污染水中的双氯芬酸(DCF)。研究发现,Fe(II)/PAA 体系在中性条件下能有效地去除 DCF,这比经典的芬顿工艺有显著的优势。根据清除实验的结果,羟基自由基和过氧自由基都被认为是 DCF 降解的原因。考察了初始 pH 值、Fe(II) 用量、PAA 浓度和常见水基质等几种操作参数对 DCF 去除的影响。在温和条件(pH 6-7)下,80%的 DCF 在 60 秒内被去除,随着 Fe(II) 用量和 PAA 浓度的增加,其去除率得到提高。和天然有机物(NOM)的存在被证明对 DCF 的降解有显著的负面影响。根据检测到的反应产物,提出了 DCF 的四条可能的降解途径,包括羟基化、C-N 键断裂、脱羧和脱氢。

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