4.6 Article

Highly Active CuO/KCC-1 Catalysts for Low-Temperature CO Oxidation

期刊

PROCESSES
卷 10, 期 1, 页码 -

出版社

MDPI
DOI: 10.3390/pr10010145

关键词

air pollution control; CuO; dendritic mesoporous silica; CO oxidation; sintering resistance

资金

  1. National Natural Science Foundation of China [21976078]
  2. Natural Science Foundation of Jiangxi Province [20202ACB213001]
  3. Graduate Students Innovation Special Foundation of Jiangxi Province [CX2018035]

向作者/读者索取更多资源

In this study, CuO catalysts supported on KCC-1 were successfully prepared, and it was found that 5% CuO loading showed the best activity for CO oxidation at low temperatures. The thermal stability of the catalyst was improved due to the large specific surface area and dendritic layered walls of KCC-1, which prevented the sintering of active components. Additionally, the catalyst exhibited abundant mesoporous and surface active oxygen species, enhancing the mass transfer and promoting the adsorption and decomposition of CO, leading to improved CO oxidation performance.
Copper catalysts have been extensively studied for CO oxidation at low temperatures. Previous findings on the stability of such catalysts, on the other hand, revealed that they deactivated badly under extreme circumstances. Therefore, in this work, a series of KCC-1-supported copper oxide catalysts were successfully prepared by impregnation method, of which 5% CuO/KCC-1 exhibited the best activity: CO could be completely converted at 120 degrees C. The 5% CuO/KCC-1 catalyst exhibited better thermal stability, which is mainly attributed to the large specific surface area of KCC-1 that facilitates the high dispersion of CuO species, and because the dendritic layered walls can lengthen the movement distances from particle-to-particle, thus helping to slow down the tendency of active components to sinter. In addition, the 5% CuO/KCC-1 has abundant mesoporous and surface active oxygen species, which are beneficial to the mass transfer and promote the adsorption of CO and the decomposition of Cu+-CO species, thus improving the CO oxidation performance of the catalyst.

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