催化作用
化学
阳离子聚合
苯
热液循环
氧气
降级(电信)
金属
核化学
化学工程
无机化学
高分子化学
有机化学
计算机科学
电信
工程类
作者
Wenjia Mao,Xinting Wang,Xiaoli Hu,Zihan Lin,Zhong‐Min Su
标识
DOI:10.1021/acs.iecr.1c02259
摘要
Two novel Co-based metal–organic frameworks, namely, [Co3(H3bpt)2(1,4-bimb)3(H2O)2]·2DMF·H2O (CUST-560) and [Co3(H3bpt)2(4,4′-tmdp)2(H2O)2]·2CH3OH·H2O (CUST-561) (H3bpt = 3,4′,5-biphenyltricarboxylic 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·– 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.
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