Reaction gas treatment promoting activity and stability of PdO for lean methane oxidation over phosphorus modified Pd/Al2O3 catalysts

被引:2
作者
Yan, Lu [1 ]
Chen, Rongzhou [1 ]
Wei, Haisheng [2 ]
Zhou, Yanliang [3 ]
Hong, Bilv [1 ]
Yang, Yijia [1 ]
Zheng, Ying [1 ]
Huang, Fei [1 ]
机构
[1] Fujian Normal Univ, Coll Chem & Mat Sci, Fujian Prov Key Lab Adv Mat Oriented Chem Engn, Fujian Prov Key Lab Polymer Mat, Fuzhou 350007, Fujian, Peoples R China
[2] Yantai Univ, Dept Coll Chem & Chem Engn, Yantai 264005, Shandong, Peoples R China
[3] 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
Phosphorus; Pd; Alumina; Lean CH4 oxidation; Metal-support interaction; SUPPORTED PALLADIUM CATALYSTS; PHASE-TRANSFORMATION; COMBUSTION; WATER; ALUMINA; PERFORMANCE; KINETICS; EFFICIENT; REDUCTION; DYNAMICS;
D O I
10.1016/j.ijhydene.2023.03.116
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
Pretreatment under specific atmosphere is a general strategy to activate catalysts. How physicochemical properties of supports are modulated during activation process and their influence on active sites are still the ongoing topic. Herein, the effect of reaction gas treatment on performance of phosphorus modified Pd/Al2O3 catalysts in lean methane oxidation was studied. The pretreated Pd/P-doped Al2O3 catalyst exhibited a full conversion of CH4 at similar to 400 degrees C, excellent stability under both dry and wet conditions. Characterization results reveal that the uniform and stable P species in Al2O3 enhanced the metal-support interaction and availability of oxygen in support. Under reaction gas condition, PdO-support connection was further promoted to favor generation of oxygen vacancies on support with the help of CH4, leading to weakened Pd-O bond, facile reformation and increased fraction of PdO. These facilitated formation of intermediates and surface dehydroxylation and mitigated the deactivation caused by thermodynamic decomposition of PdO. (c) 2023 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:23516 / 23529
页数:14
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