Affiliation:
1. Faculty of Metallurgical and Energy Engineering, Kunming University of Science and Technology, Kunming 650093, China
2. State-Local Joint Engineering Research Center of Precious Metal Catalytic Technology and Application, Kunming Sino-Platinum Metals Catalysts Co., Ltd., Kunming 650106, China
3. Yunnan Precious Metal Laboratory Co., Ltd., Kunming 650100, China
4. State Key Laboratory of Advanced Technologies for Comprehensive Utilization of Platinum Metals, Kunming Institute of Precious Metals, Kunming 650100, China
Abstract
The properties of a catalyst support are closely related to the catalyst activity, yet the focus is often placed on the active species, with little attention given to the support properties. In this work, we specifically investigated the changes in support properties after the addition of P, as well as their impact on catalyst activity when used for catalyst preparation. We prepared the CeO2-ZrO2-P2O5-Al2O3 (CeZrPAl) composite oxides using the sol–gel, impregnation, and mechanical mixing methods, and characterized the support properties using techniques such as XRD, XPS, SEM-EDS, N2 adsorption–desorption, and Raman spectra. The results showed that the support prepared using the sol–gel method can exhibit a more stable phase structure, larger surface area, higher adsorption capacity for oxygen species, and greater oxygen storage capacity. The addition of an appropriate amount of P is necessary. On the one hand, the crystallization and growth of CePO4 can lead to a decrease in the Ce content in the cubic phase ceria–zirconia solid solution, resulting in a phase separation of the ceria–zirconia solid solution. On the other hand, CePO4 can lock some of the Ce3+/Ce4+ redox pairs, leading to a reduction in the adsorption of oxygen species and a decrease in the oxygen storage capacity of the CeZrPAl composite oxides. The research results indicated that the optimal P addition is 6 wt.% in the support. Therefore, we prepared a Pd/CeZrPAl catalyst using CeZrAl with 6 wt.% P2O5 as the support and conducted the catalytic oxidation of C3H8. Compared with the support without P added, the catalyst activity of the support loaded with P was significantly improved. The fresh and aged (1000 °C/5 h) catalysts decreased by 20 °C and 5 °C in T50 (C3H8 conversion temperature of 50%), and by 81 °C and 15 °C in T90 (C3H8 conversion temperature of 90%), respectively.
Funder
National Natural Science Foundation of China
Major Science and Technology Project of Yunnan Province
Scientific and Technological Project of Yunnan Precious Metals Laboratory
Chongqing Technology Innovation and Application Development Project
Technology Talents and Platform Project of Yunnan
Yunnan Fundamental Research Projects
Reference57 articles.
1. Oxidation of C3H8, iso-C5H12 and C3H6 under near-stoichiometric and Fuel-lean conditions over aged Pt-Pd/Al2O3 catalysts with different Pt:Pd ratios;Kim;Appl. Catal. B,2019
2. Insights and comparison of structure-property Khudorozhkov, A.K.; Chetyrin, I.A.; Bukhtiyarov, A.V.; Prosvirin, I.P.; Bukhtiyarov, V.I. Propane oxidation over Pd/Al2O3: Kinetic and in situ XPS study;Cargnello;Top. Catal.,2017
3. The promoting effect of Nb2O5 addition to Pd/Al2O3 catalysts on propane oxidation;Noronha;Catal. Today,2000
4. Core-shell nanocatalyst design by combining high-throughput experiments and first-principles simulations;Peela;Chemcatchem,2013
5. Effect of secondary additives on the properties of vanadium-aluminum mixed oxide tableted catalysts used in the oxidation of propane;Farin;Powder Technol.,2021
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献