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采用磁性碳异质结催化剂分解过一硫酸盐实现对扑热息痛的光辅助催化降解。

Photo-assisted catalytic degradation of acetaminophen using peroxymonosulfate decomposed by magnetic carbon heterojunction catalyst.

机构信息

Research Center for Health, Safety and Environment, Alborz University of Medical Sciences, Karaj, Iran; Department of Environmental Health Engineering, Alborz University of Medical Sciences, Karaj, Iran.

College of Science and Engineering, Flinders University, Clovelly Park, SA, 5042, Australia.

出版信息

Chemosphere. 2019 Oct;232:140-151. doi: 10.1016/j.chemosphere.2019.05.070. Epub 2019 May 16.

Abstract

Catalytic oxidative degradation of acetaminophen (ACT) was evaluated using magnetic mesoporous carbon (MNPs@C) coupled with UV light and peroxymonosulfate (PMS). The performance of hybrid system (i.e., MNPs@C/UV/PMS) was assessed as a function of some operational factors (e.g., reaction time and different concentrations of catalyst, PMS and ACT) in a batch system. MNPs@C represented a high magnetic response and was easily recovered from aqueous solution via an external magnet. A significant synergistic effect was observed among the applied techniques in MNPs@C/UV/PMS system for ACT degradation. After 40 min reaction, the removal efficiencies of 97.4 and 63.5% were obtained for ACT and TOC, respectively. Both adsorption and oxidation mechanisms were responsible simultaneously for ACT removal in MNPs@C/UV/PMS system. Under optimum conditions, the removal rates of ACT and TOC were reduced slightly to 91.7 and 49.4% after five consecutive catalyst uses, which indicates the excellent reusing potential of MNPs@C. In addition, a high stability was detected for as-prepared catalyst during recycling tests, since the quantity of leached Fe was <0.2 mg/L. Methanol and tert-butyl alcohol showed a strong quenching effect on the performance of MNPs@C/UV/PMS system, demonstrating the dominant role of SO and HO radicals in ACT degradation process. MNPs@C in comparison with ferrous ions, as a homogeneous catalyst, showed a better performance in the activation of PMS and ACT degradation. Integration of MNPs@C, UV and PMS exhibited an excellent performance into ACT removal over 40 min reaction, which can be utilized as an effective and promising technique for the efficient decontamination of polluted waters.

摘要

采用磁介孔碳(MNPs@C)耦合紫外光和过一硫酸盐(PMS)评价了对乙酰氨基酚(ACT)的催化氧化降解。在批处理系统中,作为一些操作因素(例如反应时间以及催化剂、PMS 和 ACT 的不同浓度)的函数,评估了混合系统(即 MNPs@C/UV/PMS)的性能。MNPs@C 表现出高磁响应性,并且通过外部磁铁可从水溶液中容易地回收。在所应用的技术中,在 MNPs@C/UV/PMS 体系中观察到显著的协同效应,用于 ACT 降解。在 40min 反应后,ACT 和 TOC 的去除效率分别为 97.4%和 63.5%。吸附和氧化机制在 MNPs@C/UV/PMS 体系中同时负责 ACT 的去除。在最佳条件下,ACT 和 TOC 的去除率在连续使用五次后略有降低,分别为 91.7%和 49.4%,这表明 MNPs@C 具有优异的再利用潜力。此外,在回收试验中,检测到所制备的催化剂具有很高的稳定性,因为浸出的 Fe 量<0.2mg/L。甲醇和叔丁醇对 MNPs@C/UV/PMS 体系的性能表现出强烈的猝灭作用,表明 SO 和 HO 自由基在 ACT 降解过程中起主导作用。与二价铁离子相比,MNPs@C 作为均相催化剂,在 PMS 和 ACT 降解的活化中表现出更好的性能。MNPs@C、UV 和 PMS 的集成在 40min 反应内表现出对 ACT 去除的优异性能,可作为一种有效且有前途的技术,用于受污染水的有效净化。

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