Activation of Peroxymonosulfate by Co-Metal-Organic Frameworks as Catalysts for Degradation of Organic Pollutants

被引:10
作者
Mao, Wenjia [1 ,2 ]
Wang, Xinting [1 ,2 ]
Hu, Xiaoli [1 ,2 ]
Lin, Zihan [1 ]
Su, Zhongmin [1 ,2 ,3 ]
机构
[1] Changchun Univ Sci & Technol, Sch Chem & Environm Engn, Changchun 130022, Peoples R China
[2] Jilin Prov Sci & Technol Innovat Ctr Opt Mat & Ch, Changchun 130022, Peoples R China
[3] Joint Sino Russian Lab Opt Mat & Chem, Changchun 130022, Peoples R China
基金
中国国家自然科学基金;
关键词
HETEROGENEOUS ACTIVATION; ADVANCED OXIDATION; PHOTOCATALYTIC DEGRADATION; POROUS CARBON; DYES; WATER; PMS; PHOTODEGRADATION; CONTAMINANTS; ENHANCEMENT;
D O I
10.1021/acs.iecr.1c02259
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Two novel Co- based metal-organic frameworks, namely, [Co-3( H(3)bpt) 2( 1,4- bimb) 3(H2O)(2)] center dot 2DMF center dot H2O (CUST-560) and [Co-3(H(3)bpt)2(4,4'-tmdp)2(H2O)(2)]center dot 2CH(3)OH center dot H2O (CUST-561) (H(3)bpt = 3,4',5biphenyltricarboxylic acid, 4,4'-tmdp = 4,4-trimethylenedipyridine, and 1,4-bimb = 1,4-bis((1H-imidazol-1-yl)methyl)benzene), were synthesized under hydrothermal conditions and characterized. In this study, by adjusting several experimental parameters including catalyst dosage, PMS volume, temperature, and the initial value of pH, PMS activation toward two cationic dyes and two anionic dye degradations was systematically examined. Radical scavenging experiments revealed that SO4 center dot- is considered to act as the paramount reactive oxygen species in the oxidation process. The Co(III)/Co(II) recycle of CUST-560 and CUST-561 is able to carry out an effective electronic transfer to PMS, facilitating the reaction process; thus, an eminent catalytic property has emerged. Consequently, the original material as-synthesized is thought to be a splendid activator to peroxymonosulfate activation for extermination and decolorization of dyes.
引用
收藏
页码:13223 / 13232
页数:10
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