Low-temperature CO preferential oxidation in H2-rich stream over iron modified Pd-Cu/ hydroxyapatite catalyst

被引:14
|
作者
Li, Xiao [1 ,2 ]
Xing, Lisha [1 ,2 ]
Zhao, Wanjun [1 ,2 ]
Wang, Yongzhao [1 ]
Zhao, Yongxiang [1 ]
机构
[1] Shanxi Univ, Engn Res Ctr, Minist Educ Fine Chem, Taiyuan 030006, Peoples R China
[2] Shanxi Univ, Sch Chem & Chem Engn, Taiyuan 030006, Peoples R China
基金
中国国家自然科学基金;
关键词
CO preferential oxidation; Low-temperature; Pd-Cu; hydroxyapatite; Iron modification; DOPED CERIA; PD-CU-CL-X/AL2O3; CATALYST; ROOM-TEMPERATURE; CUO/CEO2; H-2-RICH STREAMS; PERFORMANCE; COPPER; FE; HYDROGEN; OXIDE;
D O I
10.1016/j.ijhydene.2021.06.156
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
The effect of FeCl3 addition on the catalytic property of Pd-Cu/hydroxyapatite (Pd-Cu/ HAP) for low-temperature CO preferential oxidation (CO-PROX) under H2-rich condition has been investigated. It can be found that CO conversion of Pd-Cu/HAP rapidly decreases from 56% to 21% within 2 hat 30 degrees C in the presence of water, however, the Pd-Cu-Fe/HAP with the Fe/Cu atomic ratio of 1:1 presents a stable CO conversion of 40% and CO2 selectivity of 100% under the same reaction conditions. The characterization results display that the addition of FeCl3 to Pd-Cu/HAP causes the formation of Fe2O3 species, and the strong interaction presents between Fe2O3 species and Pd-Cu/HAP. Thus, the Pd0 species generated during CO-PROX over Pd-Cu-Fe/HAP can be more easily oxidized than that over Pd-Cu/HAP, which could avoid H2 adsorption on Pd0 species and maintain CO adsorption and activation. (c) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved. <comment>Superscript/Subscript Available</comment
引用
收藏
页码:29940 / 29950
页数:11
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