Solvothermal synthesis of MIL-53Fe@g-C3N4 for peroxymonosulfate activation towards enhanced photocatalytic performance

被引:18
|
作者
Li, Hongmiao [1 ]
Li, Di [1 ]
Long, Mingyang [1 ]
Bai, Xiaojuan [3 ]
Wen, Qi [1 ]
Song, Fang [2 ]
机构
[1] Xian Univ Architecture & Technol, Sch Chem & Chem Engn, Xian 710055, Peoples R China
[2] Xian Univ Architecture & Technol, Instrument Anal Ctr Xian Univ Architecture & Techn, Xian 710055, Peoples R China
[3] Beijing Univ Civil Engn & Architecture, Key Lab Urban Stormwater Syst & Water Environm, Minist Educ, Beijing 100044, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalysis; Peroxymonosulfate; Visible light; Degradation; SELECTIVE OXIDATION; DEGRADATION; MIL-53(FE); MOF;
D O I
10.1016/j.colsurfa.2022.130646
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The MIL-53Fe@g-C3N4 samples were prepared by solvothermal method and recorded as CM-x. The potocatalytic activity of the MIL-53Fe@g-C3N4 was significantly higher than MIL-53Fe, and it might be due to the successfully constructed heterojunction promoting the migration and separation effciency of photo-generated electron and hole pairs. In order to further enhance the potocatalytic activity of the MIL-53Fe@g-C3N4, peroxymonosulfate was introduced into the MIL-53Fe@g-C3N4/Vis system, and the peroxymonosulfate could be simultaneously activated by photogenerated electron and iron to form sulfate radical under visible light irradiation. Therefore, the degradation efficiency of oxytetracycline hydrochloride was enhanced obviously. Meantime, the effects of peroxymonosulfate dosage, oxytetracycline hydrochloride concentration, temperature and pH on the degrada-tion efficiency of oxytetracycline hydrochloride were studied systematically. Meanwhile, the free radical catching experiments and electron spin resonance analysis confirmed that the main active substances were sulfate radical and hole. Finally, the mechanism and possible degradation pathways of MIL-53Fe@g-C3N4 acti-vating peroxymonosulfate to degrade oxytetracycline hydrochloride were proposed.
引用
收藏
页数:12
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