催化作用
煅烧
羟基自由基
化学
单线态氧
共沉淀
激进的
刚果红
核化学
钼酸盐
吸附
无机化学
氧气
有机化学
作者
Huimin Zhou,Yang Qiu,Chuanxi Yang,Jinqiu Zang,Zihan Song,Tingzheng Yang,Jinzhi Li,Yuqi Fan,Feng Dang,Weiliang Wang
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2022-12-07
卷期号:27 (24): 8642-8642
被引量:26
标识
DOI:10.3390/molecules27248642
摘要
In order to improve the catalytic activity of cobalt molybdate (CoMoO4), a PDS-activated and UV-vis assisted system was constructed. CoMoO4 was prepared by coprecipitation and calcination, and characterized by XRD, FTIR, Raman, SEM, TEM, XPS, TGA Zeta potential, BET, and UV-Vis DRS. The results showed that the morphology of the CoMoO4 nanolumps consisted of stacked nanosheets. XRD indicated the monoclinic structures with C2/m (C32h, #12) space group, which belong to α-CoMoO4, and both Co2+ and Mo6+ ions occupy distorted octahedral sites. The pH of the isoelectric point (pHIEP) of CMO-8 at pH = 4.88 and the band gap of CoMoO4 was 1.92 eV. The catalytic activity of CoMoO4 was evaluated by photo-Fenton degradation of Congo red (CR). The catalytic performance was affected by calcination temperature, catalyst dosage, PDS dosage, and pH. Under the best conditions (0.8 g/L CMO-8, PDS 1 mL), the degradation efficiency of CR was 96.972%. The excellent catalytic activity of CoMoO4 was attributed to the synergistic effect of photo catalysis and CoMoO4-activated PDS degradation. The capture experiments and the ESR showed that superoxide radical (·O2−), singlet oxygen (1O2), hole (h+), sulfate (SO4−·), and hydroxyl (·OH−) were the main free radicals leading to the degradation of CR. The results can provide valuable information and support for the design and application of high-efficiency transition metal oxide catalysts.
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