Synergistic tuning of the phase structure of alumina and ceria-zirconia in supported palladium catalysts for enhanced methane combustion

被引:7
|
作者
Lin, Jia [1 ]
Chen, Yelin [1 ]
Huang, Jiangli [1 ]
Cai, Guohui [2 ]
Xiao, Yihong [2 ]
Zhan, Yingying [2 ]
Zheng, Ying [1 ]
机构
[1] Fujian Normal Univ, Coll Chem & Mat Sci, Fujian Prov Key Lab Adv Mat Oriented Chem Engn, Fuzhou 350007, Fujian, Peoples R China
[2] Fuzhou Univ, Natl Engn Res Ctr Chem Fertilizer Catalyst, Fuzhou 350002, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
Methane combustion; Pd-based catalysts; CeO2-ZrO2-Al2O3 composite oxides; Phase structure; Surface property; CONTROLLABLE SYNTHESIS; ACTIVE-SITES; CO OXIDATION; MIXED OXIDES; TEMPERATURE; PD; PD/AL2O3; BEHAVIOR; DECOMPOSITION; RESISTANCE;
D O I
10.1016/j.ijhydene.2021.07.151
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
CeO2-ZrO2-Al2O3 composite oxides supported palladium catalysts (Pd/CZA) are promising candidates for catalytic oxidation reactions. However, the efficient and stable oxidation of methane over Pd-based catalysts remains a longstanding challenge. Herein, we present a facile strategy to boost the catalytic performance of Pd/CZA through elaborately tuning the phase structure of supports. Calcining supports at relatively high temperatures (1200, 1300 degrees C) induced the phase transition of alumina (from gamma- to alpha-) and the development of CeO2-ZrO2 solid solution (CZ). The weak interaction between alpha-Al2O3 and PdO resulted in an improved reducibility of catalysts. Meanwhile, the higher oxygen mobility originated from well-crystallized CZ phase contributed to the reoxidation of Pd to PdO, giving rise to abundant surface active Pd2+ species. Coupled with the hydrophobicity of alpha-Al2O3, the catalyst prepared with CZA supports calcined at 1300 degrees C demonstrated an excellent low-temperature activity, astounding stability and greatly enhanced water resistance towards methane combustion. (C) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:33397 / 33408
页数:12
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