臭氧氧化挥发性有机化合物的高效钴促进 V2O5/SiO2 催化剂

IF 1.7 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
D. A. Bokarev, S. A. Kanaev, G. O. Bragina, A. E. Vaulina, G. N. Baeva, A. Yu. Stakheev
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引用次数: 0

摘要

该研究证明了在 V2O5/SiO2 催化剂中添加少量 Co 以提高其在臭氧辅助催化氧化 (OZCO) 挥发性有机化合物中活性的可能性。研究发现,与参考催化剂 Co3O4/SiO2 和 V2O5/SiO2 相比,共同促进的 V2O5/SiO2 催化剂(0.5%Co w/w)在 50-100 °C 下的 n-C4H10 转化率显著提高。这是通过提高 Co 位点的 O3 分解速率实现的,该速率提高了活性原子氧物种 O* 的形成,从而加速了 OZCO 过程。共同促进的 V2O5/SiO2 催化剂在正-C4H10 的 OZCO 过程中消耗臭氧的效率很高,这是因为分子氧参与了氧化反应,并最大限度地减少了 O* 物种的意外重组。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Highly efficient cobalt-promoted V2O5/SiO2 catalyst for the oxidation of volatile organic compounds by ozone

The study demonstrates the possibility of promoting the V2O5/SiO2 catalyst with a small amount of Co to increase its activity in the ozone-assisted catalytic oxidation (OZCO) of volatile organic compounds. It was found that the conversion of n-C4H10 over the Co-promoted V2O5/SiO2 catalyst (0.5% of Co w/w) at 50–100 °C significantly increases compared to that found over the reference catalysts Co3O4/SiO2 and V2O5/SiO2. This is achieved by increasing the rate of O3 decomposition at Co sites, which enhances the formation of reactive atomic oxygen species O*, and subsequent acceleration of the OZCO process. High efficiency of ozone consumption in the OZCO of n-C4H10 over the Co-promoted V2O5/SiO2 catalyst is due to the involvement of molecular oxygen in the oxidation reaction and to minimization of undesired recombination of the O* species.

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来源期刊
Russian Chemical Bulletin
Russian Chemical Bulletin 化学-化学综合
CiteScore
2.70
自引率
47.10%
发文量
257
审稿时长
3-8 weeks
期刊介绍: Publishing nearly 500 original articles a year, by leading Scientists from Russia and throughout the world, Russian Chemical Bulletin is a prominent international journal. The coverage of the journal spans practically all areas of fundamental chemical research and is presented in five sections: General and Inorganic Chemistry; Physical Chemistry; Organic Chemistry; Organometallic Chemistry; Chemistry of Natural Compounds and Bioorganic Chemistry.
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