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基于绿色合成石墨烯的 Co-Fe 普鲁士蓝类似物作为过一硫酸盐的活化剂用于盐酸左氧氟沙星的降解。

Facile green synthetic graphene-based Co-Fe Prussian blue analogues as an activator of peroxymonosulfate for the degradation of levofloxacin hydrochloride.

机构信息

Key Laboratory for Yellow River and Huai River Water Environment and Pollution Control, Ministry of Education, Henan Key Laboratory for Environmental Pollution Control, School of Environment, Henan Normal University, Xinxiang, Henan 453007, PR China.

Key Laboratory for Yellow River and Huai River Water Environment and Pollution Control, Ministry of Education, Henan Key Laboratory for Environmental Pollution Control, School of Environment, Henan Normal University, Xinxiang, Henan 453007, PR China.

出版信息

J Colloid Interface Sci. 2018 Sep 15;526:18-27. doi: 10.1016/j.jcis.2018.04.070. Epub 2018 Apr 18.

DOI:10.1016/j.jcis.2018.04.070
PMID:29709668
Abstract

A kind of Co-Fe Prussian blue analogues (Co-Fe PBAs), cobalt hexacyanoferrate Co[Fe(CN)], and graphene oxide (GO) were combined to synthesize magnetically separable Co-Fe PBAs@rGO nanocomposites through a simple two-step hydrothermal method. The crystalline structure, morphology and textural properties of the Co-Fe PBAs@rGO nanocomposites were characterized. The catalytic performance of the nanocomposites was evaluated by PMS activation, with Levofloxacin Hydrochloride (LVF) as the target contaminant. Synergistic interactions between the Co-Fe PBAs and rGO prevented the aggregation of the Co-Fe PBAs nanoparticles, which resulted in enhanced degradation efficiencies. The influence of several critical parameters was investigated, including the reaction temperature, PMS and Co-Fe PBAs@rGO catalyst concentrations, solution pH and salt content. LVF degradation was favored at higher catalyst and PMS concentrations, high temperatures, and in neutral or weak acidic solutions. Sulphate radicals were the dominant active species in the Co-Fe PBAs@rGO/PMS system. In addition, the Co-Fe PBAs@rGO exhibited no significant decrease in LVF degradation efficiency following five catalytic cycles. Thus, the as-prepared Co-Fe PBAs@rGO nanocomposite catalyst might be applied to the removal of hard-to-degrade organics owing to its high catalytic ability to activate PMS, as well as its good reusability and recyclability.

摘要

一种钴铁普鲁士蓝类似物(Co-Fe PBAs)、钴六氰合铁 Co[Fe(CN)] 和氧化石墨烯(GO)通过简单的两步水热法结合在一起,合成了磁性可分离的 Co-Fe PBAs@rGO 纳米复合材料。对 Co-Fe PBAs@rGO 纳米复合材料的晶体结构、形貌和结构特性进行了表征。通过 PMS 活化评估了纳米复合材料的催化性能,以盐酸左氧氟沙星(LVF)为目标污染物。Co-Fe PBAs 和 rGO 之间的协同相互作用阻止了 Co-Fe PBAs 纳米粒子的聚集,从而提高了降解效率。考察了几个关键参数的影响,包括反应温度、PMS 和 Co-Fe PBAs@rGO 催化剂浓度、溶液 pH 值和盐含量。在较高的催化剂和 PMS 浓度、高温以及中性或弱酸性溶液中,LVF 降解更有利。在 Co-Fe PBAs@rGO/PMS 体系中,硫酸根自由基是主要的活性物质。此外,Co-Fe PBAs@rGO 在五个催化循环后,LVF 降解效率没有明显下降。因此,由于其对 PMS 的高催化活化能力,以及良好的可重复使用性和可回收性,所制备的 Co-Fe PBAs@rGO 纳米复合材料催化剂可能适用于去除难降解有机物。

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