Structure-activity relationships of zirconium-modified copper-based catalysts during methanol steam reforming

被引:5
|
作者
Zhang, Qing [1 ]
Li, Didi [1 ]
Jiang, Zhaocong [1 ]
Gu, Haoyuan [1 ]
Zhu, Mengyuan [1 ]
Jin, Shiqing [1 ]
Zhu, Minghui [1 ]
机构
[1] East China Univ Sci & Technol, Sch Chem Engn, State Key Lab Chem Engn, 130 Meilong Rd, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Methanol Steam Reforming; Copper-Based Catalyst; Zirconium; Metal-Support Interfacial sites; CU/ZNO/AL2O3; CATALYSTS; CO2; HYDROGENATION; HIGH-PERFORMANCE; IN-SITU; ZNO; INSIGHTS;
D O I
10.1016/j.jcat.2024.115584
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
Acknowledged as an ideal method for in situ hydrogen generation, methanol steam reforming (MSR) requires high-performance catalysts to enhance production efficiency. Herein, we prepared a series of Zr-modified Cubased catalysts by a coprecipitation method and conducted a systematic analysis of the impacts of structural variations on MSR performance. Extensive characterization reveals a strong dependence of the catalyst's surface structure on Zr content. Introducing a moderate amount of Zr to the Cu/ZnO catalysts forms ZnZrOx solid solution and increases Cu dispersion, forming more Cu-ZnZrOx and Cu-ZnO interfacial sites with higher H2 production rate. Further increases in Zr content enlarge Cu nanoparticles and multiply Cu-ZrO2 interfacial sites. The optimal catalyst with a Zn/Zr molar ratio of 5, with the richest Cu-ZnO/Cu-ZnZrOx interfacial sites, achieves the highest H2 production rate of 117.4 mmolH2 g-1cat h-1 at 200 degrees C, which is 1.3 times and 6.8 times higher than those of Cu/ZnO and Cu/ZrO2, respectively.
引用
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页数:9
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