天然有机物介导过硫酸盐光降解氟喹诺酮类抗生素机制研究
批准号:
42107073
项目类别:
青年科学基金项目(C类)
资助金额:
30.0 万元
负责人:
刘杨
依托单位:
学科分类:
环境水科学
结题年份:
2024
批准年份:
2021
项目状态:
已结题
项目参与者:
刘杨
中文摘要
氟喹诺酮类抗生素(FQs)引起的水环境污染及生态毒性效应已成为我国乃至全球面临的重大环境问题。光降解作为FQs在自然水体中的一种重要消减方式,主要面临降解效率低、产物毒性强、抑制因素多等问题。近年来,基于过硫酸盐高级氧化技术(SR-AOPs)成为水污染控制领域的研究热点。但在无固体催化剂的天然水体环境中,过硫酸盐强化FQs光降解的研究鲜有报道。申请人前期研究发现在可见光条件下,腐殖酸能有效强化过硫酸盐氧化降解FQs。据此,本项目提出构建溶解性有机质(DOM)介导过硫酸盐强化FQs光降解体系,重点探究光子/电子在FQs、DOM和过硫酸盐之间的转移规律和路径,分析DOM强化FQs光降解效能与机制;探索FQs在过硫酸盐、DOM强化作用下的降解机理及路径;评估并调控FQs降解产物残留抗菌活性及生态毒性。项目的实施可为自然光消除FQs提供应用指导,同时为SR-AOPs在自然水体中的应用提供理论支撑。
英文摘要
The water environment pollution caused by fluoroquinolone antibiotics (FQs) and its ecotoxicological effects have become a significant environmental problem facing China and the world. Photodegradation as one of the main reduction approaches of FQs in natural waters, which faces the high toxicity of photodegradation products, low photodegradation efficiency, and many significant inhibition factors. Recently, advanced oxidation processes based on sulfate radicals (SR-AOPs) have been widely developed in water treatment. However, there is rarely a report on visible-light activated persulfate to enhance organic contaminant removal under natural water without solid-catalyst. Our previous study had found that humic acid can effectively enhance the oxidative degradation of FQs by persulfate under visible-light irradiation. In view of the above, we will propose to construct a FQs photodegradation system that persulfate mediated by DOM. The key of this work will explore the transfer law and path of photons/electrons between FQs, DOM and persulfate, and analyze the efficiency and mechanism of DOM enhancing FQS photodegradation. To further explore the degradation mechanism and pathways of FQs under the action of persulfate and DOM enhancement, the residual antimicrobial activity and ecotoxicity of FQs degradation products will be also assessed and regulated. The implementation of this project will guide the application of FQs photodegradation, and provide a powerful theoretical support for the utilization of SR-AOPs in water treatment.
氟喹诺酮类抗生素(FQs)因抗菌谱广、抗菌活性强、口服性良好等特点,在人类和兽医药中被广泛应用,由该类抗生素引起的水环境污染及生态毒性效应已成为我国乃至全球面临的重大环境问题。光降解作为FQs在自然水体中的一种重要消减方式,当前面临光能利用率差、降解效率低、降解产物毒性强、环境影响因素复杂等问题。其中,溶解性有机物(DOM)作为天然水体中存在的环境本底物,被认为是影响FQs光降解的关键因子。在本项目中,将常见为腐殖酸(HA)作为光子受体和过硫酸盐活化的电子供体,构建了基于过硫酸盐强化FQs光降解体系,加快了光子/电子在HA、过硫酸盐和FQs之间的转移速率,显著提升了可见光能的利用效率,实现光敏性特征污染物FQs的快速光氧化降解,证实了三重激发态物质(*FQs)对过硫酸盐强化FQs去除的促进机制,进一步研究发现溶液中共存的HA和Fe3+均能有效促进FQs的光降解,证实了Fe(III)-HA/FQs对加快FQs光降解的内在机制,并发现Vis/Fe(III)/PDS/HA体系对不同新污染物的选择性降解特性,最后基于多重回归模型的定量构效关系(QSAR)分析方法揭示选择性降解的作用机制,最后利用T.E.S.T软件对降解产物进行了毒性数值模拟分析。
HSF1和dECM水凝胶双信号协同调控移植iPSC-NSCs的存活和分化对缺血性卒中修复的研究
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批准号:82301556
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项目类别:青年科学基金项目
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资助金额:30万元
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批准年份:2023
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负责人:刘杨
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依托单位:
国内基金
海外基金