Fe-C填料作电芬顿阴极体系降解苯酚机理研究OA
Study on the mechanism of phenol degradation by Fe-C fillers as electro-Fenton cathode system
本研究采用Fe-C填料作电芬顿阴极的方式降解废水中的苯酚,利用电芬顿促进Fe-C阴极表面的铁还原,从而改善微电解氧化活性物质生成条件,大幅提高苯酚降解率.Fe-C填料阴极可将电子转移给O2 原位生成H2O2,同时直流电流可促进微电解反应,增强Fe-C填料中Fe0腐蚀,O2在填料的碳阴极得电子通过·O-2 途径生成H2O2.Fe-C阴极还可还原Fe3+,维持体系Fe2+浓度稳定.活性物质猝灭结果表明·OH是该体系降解苯酚主要活性物质.Fe-C填料反应前后表征结果表明,Fe-C填料阴极可有效还原表面铁氧化物,减少钝化层形成.Fe-C填料作电芬顿阴极体系苯酚和COD去除率分别为77.26%和69.25%,较单独Fe-C微电解及电芬顿体系大幅提升.此外,Fe-C填料阴极具有电能消耗低和循环稳定性好的优势.
Phenol-containing wastewater is difficult to degrade,easily accumulates,and poses serious risks to humans and ecosystems.The Fe-C fillers were used as the cathode in an electro-Fenton system to degrade phenol in wastewater in this study.The electro-Fenton process promotes the reduction of iron at the Fe-C cathode surface,thereby enhancing the generation conditions for active substances in micro-electrolysis and significantly improving phenol degradation efficiency.The Fe-C filler cathode can transfer electrons to O2 to generate H2 O2 in situ.Concurrently,the direct current promotes the micro-electrolysis reaction,enhancing the corrosion of Fe0 within the Fe-C fillers.Furthermore,O2 acquires electrons at the carbon cathode of the fillers,generating H2 O2 via the·O-2 pathway.Additionally,the Fe-C cathode reduces Fe3+,sustaining a stable concentration of Fe2+in the system.The active substances quenching experiments confirmed that·OH is the dominant active substances responsible for phenol degradation in this system.Characterization of the Fe-C filler before and after reaction revealed that the Fe-C filler cathode effectively reduces surface iron oxides,mitigating passivation layer formation.In the electro-Fenton system utilizing Fe-C filler as the cathode,the phenol and COD removal rates reached 77.26%and 69.25%,respectively.This represents a significant enhancement compared to both stand-alone Fe-C micro-electrolysis and electro-Fenton systems.Additionally,the Fe-C filler cathode exhibits advantages of low energy consumption and excellent cycling stability.
王忠华;邹玉龙;黄云騂;樊一博;周杰;赵海谦
东北石油大学土木建筑工程学院,黑龙江 大庆 163318江苏荣信环保科技有限公司,江苏 南通 226009苏州科技大学环境科学与工程学院,江苏 苏州 215009苏州科技大学环境科学与工程学院,江苏 苏州 215009苏州科技大学环境科学与工程学院,江苏 苏州 215009苏州科技大学环境科学与工程学院,江苏 苏州 215009
资源环境
苯酚微电解活性物质Fe-C填料电芬顿
phenolmicro-electrolysisactive substanceFe-C fillerelectro-Fenton
《化工学报》 2026 (2)
859-868,封3,11
黑龙江省自然科学基金项目(LH2022E032)
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