光催化
罗丹明B
盐酸四环素
电子顺磁共振
催化作用
降级(电信)
复合数
材料科学
甲基橙
可见光谱
橙色G
纳米棒
纳米颗粒
核化学
介电谱
二甲酚橙
单体
电化学
光化学
化学工程
化学
纳米技术
四环素
电极
复合材料
有机化学
生物化学
电信
光电子学
抗生素
聚合物
核磁共振
物理化学
计算机科学
工程类
物理
作者
Junjie Jing,Ying Liu,Liquan Jing,Puyang Zhou,Meng Xie,Minqiang He,Junjie Yuan,Yanhua Song,Yuanguo Xu
标识
DOI:10.1016/j.colsurfa.2022.130116
摘要
Constructing the Bi3.64Mo0.36O6.55/MIL-88A(Fe) photo-Fenton degradation system with the in situ growth of Bi3.64Mo0.36O6.55 nanoparticles onto monomer MIL-88A(Fe). The composite was applied as the photocatalyst for removing tetracycline hydrochloride (TCH). The degradation rate reaches 84.48% within 30 min under visible light and the presence of H2O2, which is 1.67 times faster than that of monomer MIL-88A(Fe). The effects of pollution concentration, the consistence of H2O2, pH value and catalyst dosage of photo-degradation were explored over this process. After four cycling, Bi3.64Mo0.36O6.55/MIL-88A(Fe) exhibited excellent photocatalytic property. The catalyst also exists selectivity to Rhodamine B and methyl orange. The special layered structure of Bi3.64Mo0.36O6.55/MIL-88A(Fe) composites can effectively promote photogenerated charge transfer and accelerate the Fe3+/Fe2+ cycling effect, which was performed by electrochemical impedance spectroscopy (EIS). Furthermore, free radical capture experiment and electron spin resonance (ESR) analysis showed that •OH, h+ and •O2– showed master roles in removal of tetracycline hydrochloride. Suitable energy band structure produced more photogenerated electrons, which could promote the Fe3+/Fe2+ transformation and accelerate the system degradation of TCH. This study has provided a novel method to construct the significant potential of the Bi3.64Mo0.36O6.55/MIL-88A(Fe) photo-Fenton system in the degradation of pollutants.
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