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Catalytic Hydrolysis of CFC-12 over MoO3/ZrO2-TiO2

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Abstract

Solid acid MoO3/ZrO2-TiO2 catalysts were prepared by impregnation method, and catalytic hydrolysis of difluorodichloromethane(CFC-12) over the catalyst was studied. The presence of MoO3/ZrO2-TiO2 catalyst in polycrystalline state could be clearly observed by transmission electron microscopy (TEM). Mesopores were detected by N2 adsorption-desorption isotherms which further confirmed the MoO3/ZrO2-TiO2 structural characteristics of catalyst. The results of NH3-TPD showed that the calcination temperatures had a great influence on the acidity of the catalyst, and the weak acidic site had a strong catalytic activity for the catalytic hydrolysis of CFC-12. Moreover, ZrO2-TiO2 was highly dispersed in the MoO3 framework, suggested by powder X-ray diffraction (XRD) and N2 adsorption-desorption results. The effects of the catalyst calcination temperatures on the conversion rate of CFC-12 were studied. The effects of catalytic hydrolysis temperatures and water vapor concentration on the catalytic hydrolysis rate of CFC-12 were also studied. The solid acid MoO3/ZrO2-TiO2 was calcined at 500 °C for 3 h at a catalytic hydrolysis temperature of 400 °C and water vapor concentration of 83.18%, and catalytic hydrolysis rate of CFC-12 reached 98.65 %. The hydrolysis rate of CFC-12 remained above 65.34% after 30 hours continuous reaction.

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Acknowledgement

Yunnan Minzu University is gratefully acknowledged for providing us with the facilities for the XRD and BET study. At the same time, I would like to thank Tong Zhou, Zhiqian Li, Guoqing Ren for their help with the expriment and Professor Tiancheng Liu guidance to the experiment.

Funding

Funded by the National Natural Science Foundation of China (No.51568068), and the Young and Middle-aged Academic and Technical Leaders Reserve Talent Program (No.202105AC160054)

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Correspondence to Tiancheng Liu  (刘天成).

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Tan, X., Zhou, T., Li, Z. et al. Catalytic Hydrolysis of CFC-12 over MoO3/ZrO2-TiO2. J. Wuhan Univ. Technol.-Mat. Sci. Edit. 38, 59–64 (2023). https://doi.org/10.1007/s11595-023-2667-y

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  • DOI: https://doi.org/10.1007/s11595-023-2667-y

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