1. A CeCoO x Core/Nb 2 O 5 @TiO 2 Double‐Shell Nanocage Catalyst Demonstrates High Activity and Water Resistance for Catalytic Combustion of o ‐Dichlorobenzene
- Author
-
Haijun Zhao, Fei Zha, Weitong Ling, Zhicheng Tang, and Shilin Wu
- Subjects
010405 organic chemistry ,Chemistry ,Organic Chemistry ,Catalytic combustion ,General Chemistry ,010402 general chemistry ,01 natural sciences ,Catalysis ,Hydrothermal circulation ,0104 chemical sciences ,Nanocages ,X-ray photoelectron spectroscopy ,Chemical engineering ,Specific surface area ,Desorption ,Thermal stability - Abstract
A series of catalysts with different core-shell structures has been successfully prepared by a hydrothermal method. They consisted of CeCoOx @TiO2 (single shell), CeCoOx @Nb2 O5 (single shell) and CeCoOx @Nb2 O5 @TiO2 (double shell) core-shell nanocages and CeCoOx nanocages, in which CeCoOx was the core and TiO2 and Nb2 O5 were shells. The influence of the core-shell structure on the catalytic performance of o-dichlorobenzene was investigated by activity, water-resistance, and thermal stability tests as well as catalyst characterization. The temperatures corresponding to 90 % conversion of o-dichlorobenzene (T90 ) of CeCoOx , CeCoOx @TiO2 , CeCoOx @Nb2 O5 , and CeCoOx @Nb2 O5 @TiO2 catalysts were 415, 383, 362 and 367 °C, respectively. CeCoOx @Nb2 O5 exhibited excellent catalytic activity, mainly owing to the special core-shell structure, large specific surface area, abundant activity of Co3+ , Ce3+ , Nb5+ , strong reducibility, and more active oxygen vacancies. It can be seen that the Nb2 O5 coating can greatly improve the catalytic activity of the catalyst. In addition, due to the protective effect of the TiO2 shell on CeCoOx , CeCoOx @Nb2 O5 @TiO2 catalysts exhibited outstanding thermal and hydrothermal stability for 20 hours. The T90 of CeCoOx @Nb2 O5 @TiO2 was slightly lower than that of CeCoOx @Nb2 O5 , but it had higher stability and hydrothermal stability. Furthermore, possible reaction pathways involving the Mars-van-Krevelen (MvK) and Langmuir-Hinshelwood (L-H) models were deduced based on studies of the temperature-programmed desorption of O2 (O2 -TPD), X-ray photoelectron spectroscopy (XPS), and in situ diffuse reflectance FTIR spectroscopy (DRIFTS) characterization.
- Published
- 2021
- Full Text
- View/download PDF