催化作用
化学
罗丹明B
纳米复合材料
激进的
降级(电信)
双酚A
活性炭
高级氧化法
核化学
化学工程
有机化学
吸附
光催化
电信
环氧树脂
计算机科学
工程类
作者
Yuanyuan Li,Jingbo Feng,Yan Zhang,Chen Wang,Junjie Hao,Yukun Wang,Yinyin Xu,Xiuwen Cheng
出处
期刊:Chemosphere
[Elsevier]
日期:2022-10-30
卷期号:311: 137038-137038
被引量:21
标识
DOI:10.1016/j.chemosphere.2022.137038
摘要
Metal organic frameworks-Covalent organic frameworks (MOFs-COFs) nanocomposites could improve the catalytic performance. Herein, a novel nanocomposite catalyst (CC@Co3O4) derived from MOFs-COFs (COF@ZIF-67) was prepared on peroxymonosulfate (PMS) activation for bisphenol A (BPA) and rhodamine B (RhB) degradation. Owing to the Co species, oxygen vacancy (OV), surface hydroxyl (-OH), graphite N and ketone groups (C=O), the CC@Co3O4 exhibited higher catalytic degradation performance and total organic carbon (TOC) for BPA (93.8% and 22.3%) and RhB (98.2% and 82.5%) with a small quantity of catalyst (0.10 g/L) and low concentration of PMS (0.20 g/L) even without pH adjustment. Sulfate radicals (•SO4-), hydroxyl radicals (•OH), single oxygen (1O2), superoxide radicals (•O2-) and electron transfer process were all involved in the degradation of BPA and RhB. Among them, the degradation of BPA and RhB mainly depended on •O2- and 1O2, respectively. Meanwhile, the degradation pathways of BPA and RhB were proposed, and the biotoxicity of the degradation products was evaluated by freshwater chlorella. The results illustrated that the degradation products were environmentally friendly to organisms. In addition, the role of COF in the nanocomposites was also studied. The addition of COF remarkably improved the catalytic performance of CC@Co3O4 due to the faster electron transfer, more graphite N and C=O. Overall, this work may open the door to the development of COF-based catalysts in the field of water pollutant remediation.
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