首页|g-C3N4/Pd/Bi2WO6光催化剂协同降解苯扎贝特机理研究

g-C3N4/Pd/Bi2WO6光催化剂协同降解苯扎贝特机理研究

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利用贵金属Pd的等离子体共振效应和形貌可控Bi2WO6的光催化协同作用,通过低温水热法设计合成具有高效可见光活性的花状g-C3N4/Pd/Bi2WO6异质结复合催化剂。在可见光照射下,异质结复合催化剂光催化降解BZF的去除率均高于g-C3N4,g-C3N4/Bi2WO6,Pd/g-C3N4和Bi2WO6,其中,50%g-C3N4/Pd/Bi2WO6对 BZF 的去除率为 96%,是 Pd/g-C3N4 的 1。8 倍,g-C3N4和 Bi2WO6 的 2。7 倍。基于表征分析可知,g-C3N4/Pd/Bi2WO6复合催化剂中Bi2WO6呈现中心辐射花状纳米结构,并与层状Pd/g-C3N4连接;贵金属Pd可作为电子传输的介质,促进g-C3N4和Bi2WO6Z型异质结构的形成,有利于协同提升可见光催化活性。淬灭实验和EPR表征证实了·OH是g-C3N4/Pd/Bi2WO6催化降解BZF的主要活性物质,LC-MS/MS分结果表明羟基化作用取代贝特链是BZF降解的主要路径。
Study on g-C3N4/Pd/Bi2WO6 heterostructure and its synergistic degradation mechanism of bezafibrate
A flower-like g-C3N4/Pd/Bi2WO6 heterostructure with high visible light activity was designed and synthesized by low temperature hydrothermal method utilizing the plasmon resonance effect of noble metal Pd and the photocatalytic synergism of shape-controlled Bi2WO6.It was found that the composite of Pd/g-C3N4 and Bi2WO6 significantly enhanced removal efficiency of BZF under visible light irradiation.Further analysis of characterization showed that Bi2WO6 in g-C3N4/Pd/Bi2WO6 exhibited a central radiated flower-like nanostructure,which is connected with layered Pd/g-C3N4.The noble metal Pd could be used as the medium for electron transport to promote the formation of Z-type heterostructures between g-C3N4 and Bi2WO6,which is beneficial to cooperatively enhance the photocatalytic activity.It was confirmed that·OH was the main active species in degradation of BZF with g-C3N4/Pd/Bi2WO6 heterostructures by quenching experiments and EPR analysis.Moreover,the LC-MS/MS analysis indicated that hydroxylation with fibrate chain substituent was the main route of BZF degradation.

bezafibratePdg-C3N4Bi2WO6heterostructure

尹泽、高博熠、刘愿强、高爱舫

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河北地质大学水资源与环境学院,河北石家庄 050031

河北省水资源可持续利用与开发实验室,河北省高校生态环境地质应用技术研发中心,河北省水资源可持续利用与产业结构优化协同创新中心,河北石家庄 050031

苯扎贝特 Pd g-C3N4 Bi2WO6 异质结

河北省教育厅科研项目河北省高等学校基本科研业务费资助项目河北省高等学校基本科研业务费资助项目河北地质大学教学改革研究与实践项目

BJK2024008QN202120QN2021222023J28

2024

中国环境科学
中国环境科学学会

中国环境科学

CSTPCDCHSSCD北大核心
影响因子:2.174
ISSN:1000-6923
年,卷(期):2024.44(5)