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CMC修饰硫化纳米零价铁耦合功能微小菌群对地下水中氯代烃的协同降解机制

批准号:
22106037
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:
吴志能
依托单位:
学科分类:
水污染与控制化学
结题年份:
2024
批准年份:
2021
项目状态:
已结题
项目参与者:
吴志能

项目摘要

结项摘要

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中文摘要
针对以往去除地下水中氯代烃“纳米零价铁(nZVI)-微生物”耦合技术存在的nZVI易钝化、易团聚,电子利用率低,及nZVI-单一细菌耦合难以实现氯代烃高效、持续降解问题,本项目可控合成羧甲基纤维素修饰硫化纳米零价铁(CMC-S-nZVI),筛选新型功能微小细菌有机卤化物呼吸细菌(OHRB)和异化铁还原菌(DIRB),优化耦合试验参数,构建CMC-S-nZVI耦合OHRB及DIRB协同降解模拟地下水中典型氯代烃强化去除技术,考察去除性能。借助多种表征手段研究杂化功能材料界面复合结构;采用TEM、FCM分析细菌形貌变化及生长特性;通过气质联用仪等识别降解产物中间物种。进一步借助宏基因组学、宏转录组学和代谢组学多组学关联分析,构建代谢网络图,阐明CMC-S-nZVI耦合功能微小菌群对氯代烃的协同降解机制。本研究将为地下水中氯代烃高效、持续降解提供理论依据和技术支撑,为氯代烃原位修复提供新思路。
英文摘要
In previous “nanoscale zero-valent iron (nZVI)-microorganism” coupling technology, nZVI is easy to passivate, aggregate, and has low electron utilization efficiency, as well as nZVI coupling with single bacterium is difficult to achieve efficient, continuous degradation of chlorinated hydrocarbons in groundwater. This project aims to synthesize controllably carboxymethyl cellulose modified sulfidated nanoscale zero-valent iron (CMC-S-nZVI), and to isolate new functional ultramicrobacteria (organohalide-respiring bacteria and dissimilatory iron reducing bacteria). Then, the coupling experimental parameters are optimized, so as to construct an enhanced removal technology for typical chlorinated hydrocarbons in simulated groundwater through CMC-S-nZVI coupling OHRB and DIRB, and further to investigate its removal performance. Moreover, the interfacial composite structure of hybrid functional material is studied by means of various characterization methods, the morphology and growth characteristics of the ultramicrobacteria are analyzed by TEM and FCM, and the intermediate species of degradation products are explored by gas chromatography-mass spectrometry analysis, etc. Additionally, the metabolic map will be constucted through the association analysis of metagenomics, metabonomics and metabonomics. Finally, the synergistic degradation mechanism of CMC-S-nZVI coupling functional ultramicrobacteria can be clarified. This project will provide theoretical basis and technical support for the efficient and continuous degradation of chlorinated hydrocarbons in groundwater, and offer a new idea for the in situ remediation of chlorinated hydrocarbons.
本项目针对以往氯代烃还原材料(如纳米零价铁)在实际应用过程中存在制备成本高、易钝化失活、阻碍电子传递、修复效果差的问题。从氯代烃污染土壤中筛选出了一株新型铁还原菌Escherichia sp. F1,菌株对Fe(Ⅲ)的还原率为38.7%,具有持续的铁还原能力。全基因组测序表明菌株包含53个与Fe(Ⅲ) 还原相关的基因,2个脱卤功能相关的基因,表明菌株铁还原和氯代污染物降解的潜力。基于筛选得到的高效微米铁粉还原剂和新型铁还原菌F1,开发了一种绿色、低成本、高效的“微米铁粉-Escherichia sp. F1”耦合对氯代烃的协同强化修复技术。在最优降解条件下,协同修复技术20 d对模拟地下水中10 mg/L TCE的降解率为41.59%,对土壤中10 mg/kg TCE 28 d的降解率为86.86%。机制分析表明铁还原菌F1可调控自身功能基因表达,还原破坏微米铁粉表面铁氧化物钝化层,促进了其反应位点及内部还原活性组分暴露,实现了钝化微米铁粉的原位自驱动激活,提升耦合材料对模拟地下水及土壤中TCE的降解。项目开发的“微米铁粉-Escherichia sp. F1”耦合修复技术对实现场地氯代有机污染物的低成本绿色治理及风险管控起到了重要的推动作用。
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