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基于 Co、Cu 和 Cr 的材料作为 PMS 的活化剂来降解代表性抗生素——在水处理中的利用策略和金属浸出的警告。

Materials Based on Co, Cu, and Cr as Activators of PMS for Degrading a Representative Antibiotic-The Strategy for Utilization in Water Treatment and Warnings on Metal Leaching.

机构信息

Grupo de Investigación en Remediación Ambiental y Biocatálisis (GIRAB), Instituto de Química, Facultad de Ciencias Exactas y Naturales, Universidad de Antioquia UdeA, Medellín 050010, Colombia.

Grupo de Catalizadores y Adsorbentes (CATALAD), Instituto de Química, Facultad de Ciencias Exactas y Naturales, Universidad de Antioquia UdeA, Medellín 050010, Colombia.

出版信息

Molecules. 2023 Jun 3;28(11):4536. doi: 10.3390/molecules28114536.

DOI:10.3390/molecules28114536
PMID:37299012
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10254359/
Abstract

A chromate of copper and cobalt (Φy) was synthesized and characterized. Φy activated peroxymonosulfate (PMS) to degrade ciprofloxacin (CIP) in water. The Φy/PMS combination showed a high degrading capability toward CIP (~100% elimination in 15 min). However, Φy leached cobalt (1.6 mg L), limiting its use for water treatment. To avoid leaching, Φy was calcinated, forming a mixed metal oxide (MMO). In the combination of MMO/PMS, no metals leached, the CIP adsorption was low (<20%), and the action of SO• dominated, leading to a synergistic effect on pollutant elimination (>95% after 15 min of treatment). MMO/PMS promoted the opening and oxidation of the piperazyl ring, plus the hydroxylation of the quinolone moiety on CIP, which potentially decreased the biological activity. After three reuse cycles, the MMO still presented with a high activation of PMS toward CIP degradation (90% in 15 min of action). Additionally, the CIP degradation by the MMO/PMS system in simulated hospital wastewater was close to that obtained in distilled water. This work provides relevant information on the stability of Co-, Cu-, and Cr-based materials under interaction with PMS and the strategies to obtain a proper catalyst to degrade CIP.

摘要

合成并表征了一种铜钴铬酸盐(Φy)。Φy 活化过一硫酸盐(PMS)以降解水中的环丙沙星(CIP)。Φy/PMS 组合对 CIP 具有很强的降解能力(~15 min 内几乎完全消除)。然而,Φy 浸出了钴(1.6 mg L),限制了其在水处理中的应用。为了避免浸出,将 Φy 煅烧,形成混合金属氧化物(MMO)。在 MMO/PMS 的组合中,没有金属浸出,CIP 的吸附量低(<20%),SO•起主要作用,对污染物的去除具有协同效应(处理 15 min 后>95%)。MMO/PMS 促进了哌嗪环的开环和氧化,以及 CIP 喹诺酮部分的羟化,这可能降低了其生物活性。经过三次重复使用循环后,MMO 仍能在 15 min 内高效活化 PMS 降解 CIP(90%)。此外,在模拟医院废水中,MMO/PMS 体系对 CIP 的降解与在蒸馏水中的降解情况相近。本工作为 Co、Cu 和 Cr 基材料与 PMS 相互作用下的稳定性以及获得合适的催化剂来降解 CIP 提供了相关信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d7c/10254359/8db703db4ea9/molecules-28-04536-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d7c/10254359/8db703db4ea9/molecules-28-04536-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d7c/10254359/8db703db4ea9/molecules-28-04536-g004.jpg

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