期刊
ACS OMEGA
卷 3, 期 12, 页码 16769-16776出版社
AMER CHEMICAL SOC
DOI: 10.1021/acsomega.8b02556
关键词
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资金
- National Natural Science Foundation of China [21878053]
- National Key RAMP
- D Program of China [2018YFA0209301]
- Natural Science Foundation of Fujian Province [2016J01057, 2017J01414]
Making use of synergy between urea and citric acid, a core-shell Pd@CeO2 catalyst with spherical morphology was facilely synthesized by a hydrothermal method. The formation mechanism of the core-shell structure in the presence of citric acid and hydrogen peroxide was studied. Results showed that the Pd@CeO2 catalyst exhibited high catalytic activity in methane oxidation. Pd nanoparticles were well stabilized by CeO2 shell encapsulation, resulting in high stability of the catalyst. A high CH4 conversion of 99% was retained after 50 h on-stream reaction at 500 degrees C. Additionally, many tiny pores on the CeO2 shell surface were beneficial for the full contact between reactants and active components. Pd nanoparticles were highly dispersed inside the shell, improving the utilization efficiency of active components. The results also demonstrated that the Pd species in the catalyst existed in the form of oxidation state, mainly in PdO (ca. 66.6%), which played an essential part in methane combustion.
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