化学
过氧乙酸
双金属片
激进的
催化作用
核化学
羟基化
过硫酸盐
降级(电信)
金属有机骨架
浸出(土壤学)
纳米材料基催化剂
无机化学
有机化学
过氧化氢
吸附
电信
环境科学
计算机科学
土壤科学
土壤水分
酶
作者
Gaofeng Zhou,Yiqing Liu,Runyu Zhou,Li Zhang,Yongsheng Fu
出处
期刊:Chemosphere
[Elsevier]
日期:2024-02-01
卷期号:349: 140958-140958
被引量:1
标识
DOI:10.1016/j.chemosphere.2023.140958
摘要
A novel 3D bimetallic metal-organic framework (MOF(Fe–Co)) was successfully prepared and its performance on sulfamethoxazole (SMX) removal in advanced oxidation process (AOP) based on peracetic acid (PAA) was evaluated. MOF(Fe–Co) exhibited an efficient catalytic performance on PAA activation for SMX degradation under neutral condition. Increasing PAA concentration could enhance SMX removal, while the variation of MOF(Fe–Co) dosage from 0.05 to 0.2 g/L had an inappreciable effect on SMX removal. According to the results of inductively coupled plasma mass spectrometry analyses and X-ray photoelectron spectroscopy, catalytic reactions mainly occurred on the surface of MOF(Fe–Co). Organic radicals (i.e., CH3C(O)OO• and CH3C(O)O•) were demonstrated to be the predominant reactive radicals for SMX degradation by MOF(Fe–Co)/PAA through radical quenching experiments. The presence of Cl− could enhance the degradation of SMX by MOF(Fe–Co)/PAA, while HCO3− and natural organic matter inhibited SMX degradation severely. Five identified degradation products were detected in this system and four possible SMX transformation pathways were proposed, including amino oxidation, S–N bond cleavage, coupling reaction and hydroxylation.
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