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生物合成纤铁矿@生物炭复合材料作为非均相类 Fenton 催化剂用于磺胺类抗生素的降解。

Biosynthesized Schwertmannite@Biochar composite as a heterogeneous Fenton-like catalyst for the degradation of sulfanilamide antibiotics.

机构信息

College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing, 210095, China.

College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing, 210095, China.

出版信息

Chemosphere. 2021 Mar;266:129175. doi: 10.1016/j.chemosphere.2020.129175. Epub 2020 Dec 17.

Abstract

Schwertmannite was successfully loaded onto biochar (Sch@BC) using a biosynthetic method. The physicochemical properties and structural morphology of Sch@BC were explored using XRD, SEM, BET, and XPS. The results showed that introducing biochar can effectively prevent the agglomeration of Sch. The catalytic activity of Sch@BC in the Fenton-like degradation of sulfamethoxazole (SMX) was also systematically investigated under different reaction conditions. Under optimum conditions ([SMX] = 10 mg L, [HO] = 2.0 mM, Sch@BC = 1.0 g L and initial pH = 3.0), the removal efficiencies of the SMX and total organic carbon (TOC) were 100% and 45.9%, respectively, within 60 min of the reaction. The results of the radical scavenger effect and ESR studies suggested that the SMX degradation in the Sch@BC/HO system was dominated by a heterogeneous Fenton-like reaction. The repeated use of Sch@BC for SMX degradation demonstrated its reusability and stability in Fenton-like reactions. There was also speculation about the degradation mechanism and pathways of SMX. Furthermore, under the same conditions, the removal efficiencies of sulfadiazine (SD) and sulfisoxazole (SIZ) under Fenton-like degradation in the Sch@BC system were 91% and 93%. The results provide a theoretical basis and practical guidance for the creation of a new catalyst using biochar as a support material for the degradation of sulfanilamide antibiotics.

摘要

采用生物合成法成功地将水铁矿负载到生物炭上(Sch@BC)。利用 XRD、SEM、BET 和 XPS 研究了 Sch@BC 的物理化学性质和结构形态。结果表明,引入生物炭可以有效地防止水铁矿的团聚。还在不同反应条件下系统研究了 Sch@BC 在类芬顿降解磺胺甲恶唑(SMX)中的催化活性。在最佳条件下([SMX] = 10 mg L,[HO] = 2.0 mM,Sch@BC = 1.0 g L 和初始 pH = 3.0),反应 60 min 内 SMX 和总有机碳(TOC)的去除效率分别达到 100%和 45.9%。自由基清除剂效应和 ESR 研究的结果表明,SMX 在 Sch@BC/HO 体系中的降解主要由非均相类芬顿反应控制。Sch@BC 重复用于 SMX 降解表明其在类芬顿反应中的可重复使用性和稳定性。还对 SMX 的降解机制和途径进行了推测。此外,在相同条件下,Sch@BC 体系中 Fenton 类降解对磺胺嘧啶(SD)和磺胺异恶唑(SIZ)的去除效率分别为 91%和 93%。研究结果为以生物炭为支撑材料的磺胺类抗生素降解新型催化剂的创制提供了理论依据和实践指导。

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