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Ag 掺杂 BiFeO 复合材料对过硫酸盐的非均相活化及其对四环素的降解作用。

Heterogeneous activation of persulfate by Ag doped BiFeO composites for tetracycline degradation.

机构信息

College of Environmental Science and Engineering, Hunan University, Changsha 410082, PR China; Key Laboratory of Environmental Biology and Pollution Control (Hunan University), Ministry of Education, Changsha 410082, PR China.

College of Environmental Science and Engineering, Hunan University, Changsha 410082, PR China; Key Laboratory of Environmental Biology and Pollution Control (Hunan University), Ministry of Education, Changsha 410082, PR China.

出版信息

J Colloid Interface Sci. 2020 Apr 15;566:33-45. doi: 10.1016/j.jcis.2020.01.012. Epub 2020 Jan 7.

DOI:10.1016/j.jcis.2020.01.012
PMID:31986307
Abstract

Persulfate (PS) activation have been extensively considered as a promising technology for removing recalcitrant pollutants, due to their production of radicals with superior oxidation reactivity. However, a catalyst with high reactive and convenient recovery for PS activation still remains to be developed. In this work, the silver-doped bismuth ferrite (Ag-BiFeO, x = 0.1, 0.2, 0.3 and 0.4) catalysts with variable Ag content were synthesized via a facile sol-gel method and applied as heterogeneous catalyst in PS activation for tetracycline (TC) degradation. Ag-BiFeO presented the best catalytic activity compared with other Ag doped BiFeO composites, 91% TC could be efficiently removed within 60 min under optimized conditions and the reaction rate constant was 0.0338 min. On the basis of the characterization analysis and catalytic test results, Ag could be the effective active site in PS activation and had a significant effect on PS activation. Moreover, the initial pH has negligible effect on the catalytic performance, indicating that Ag-BiFeO/PS system could work in a wide pH range. The results of electron spin-resonance spectroscopy and radical quenching tests suggested that both SO and OH radicals were involved in the Ag-BiFeO/PS system. The possible mechanism of Ag-BiFeO activating PS and the major degradation pathway of TC degradation were proposed. At last, the reusability experiment results proved that Ag-BiFeO catalyst still has a high catalytic performance after 4 times used.

摘要

过硫酸盐(PS)活化因其产生具有较高氧化反应活性的自由基而被广泛认为是去除难降解污染物的一种很有前途的技术。然而,对于 PS 活化,仍需要开发具有高反应活性和方便回收的催化剂。在这项工作中,通过简便的溶胶-凝胶法合成了具有不同 Ag 含量的银掺杂铋铁氧体(Ag-BiFeO,x=0.1、0.2、0.3 和 0.4)催化剂,并将其作为非均相催化剂应用于 PS 活化去除四环素(TC)。与其他 Ag 掺杂 BiFeO 复合材料相比,Ag-BiFeO 表现出最好的催化活性,在优化条件下,60 min 内可有效去除 91%的 TC,反应速率常数为 0.0338 min。基于表征分析和催化试验结果,Ag 可能是 PS 活化的有效活性位,对 PS 活化有显著影响。此外,初始 pH 值对催化性能的影响可以忽略不计,这表明 Ag-BiFeO/PS 体系可以在较宽的 pH 范围内工作。电子顺磁共振光谱和自由基猝灭试验的结果表明,SO 和 OH 自由基都参与了 Ag-BiFeO/PS 体系。提出了 Ag-BiFeO 活化 PS 的可能机制和 TC 降解的主要途径。最后,重复使用实验结果证明,Ag-BiFeO 催化剂在重复使用 4 次后仍具有较高的催化性能。

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