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深入了解酒石酸增强均相和非均相铜催化类芬顿体系的作用机制。

New insights into the mechanisms of tartaric acid enhancing homogeneous and heterogeneous copper-catalyzed Fenton-like systems.

机构信息

College of Architecture & Environment, Sichuan University, Chengdu 610065, China.

College of Environmental Science and Engineering, Nankai University, Tianjin 300071, China.

出版信息

J Hazard Mater. 2021 Apr 5;407:124351. doi: 10.1016/j.jhazmat.2020.124351. Epub 2020 Oct 22.

Abstract

The specific roles of tartaric acid (TA), as an eco-friendly ligand, in homogeneous and heterogeneous copper-catalyzed systems were systematically revealed and new mechanisms of TA enhancing the three Fenton-like processes were proposed to provide a theoretical significance in overcoming the deficiency of conventional Fenton processes. The results identified hydroxyl radical (•OH) as the main species responsible for the simultaneous decomposition of TA and metronidazole (MNZ) according to TOC removal. The ESR technique was used to detect superoxide radicals (•O), carbon-centered radical (•R) and hydrogen radical (•H) in the Cu/TA/HO system, which contributed to the acceleration of the Cu/Cu redox cycle. The enhancing effect of TA on the homogeneous process was ascribed to the formation of a soluble complex with Cu, which favored the pH range extension, Cu oxidation, and radical generation. Moreover, the adsorption of TA on the catalysts surface promoted the consumption of HO, inducing •OH generation. The formed surface complex (≡Cu-TA) also accelerated the regeneration of ≡Cu, which was confirmed by density functional theory (DFT) calculation and surface characterization analysis (SEM, XRD, and XPS). The possible degradation pathways of MNZ in TA-modified Fenton-like system were also clarified.

摘要

系统揭示了酒石酸(TA)作为一种环保配体在均相和多相铜催化体系中的具体作用,并提出了 TA 增强三种类 Fenton 过程的新机制,为克服传统 Fenton 过程的缺陷提供了理论意义。根据 TOC 去除率,结果确定了羟基自由基(•OH)是同时分解 TA 和甲硝唑(MNZ)的主要物质。ESR 技术用于检测 Cu/TA/HO 体系中的超氧自由基(•O)、碳中心自由基(•R)和氢自由基(•H),这有助于加速 Cu/Cu 氧化还原循环。TA 对均相过程的增强作用归因于与 Cu 形成可溶性配合物,有利于扩展 pH 范围、Cu 氧化和自由基生成。此外,TA 在催化剂表面的吸附促进了 HO 的消耗,诱导•OH 的生成。形成的表面配合物(≡Cu-TA)也加速了≡Cu 的再生,这通过密度泛函理论(DFT)计算和表面特征分析(SEM、XRD 和 XPS)得到了证实。还阐明了 TA 改性类 Fenton 体系中 MNZ 的可能降解途径。

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