Overcoming the kinetic and deactivation limitations of Ni catalyst by alloying it with Zn for the dry reforming of methane

被引:23
|
作者
Velisoju, Vijay K. [1 ]
Virpurwala, Quaid Johar Samun [1 ]
Attada, Yerrayya [1 ]
Bai, Xueqin [1 ]
Davaasuren, Bambar [2 ]
Ben Hassine, Mohamed [2 ]
Yao, Xueli [1 ]
Lezcano, Gontzal [1 ]
Kulkarni, Shekhar R. [1 ]
Castano, Pedro [1 ,3 ]
机构
[1] King Abdullah Univ Sci & Technol KAUST, KAUST Catalysis Ctr KCC, Multiscale React Engn, Thuwal 239556900, Saudi Arabia
[2] King Abdullah Univ Sci & Technol KAUST, Imaging & Characterizat Core Lab, Thuwal 239556900, Saudi Arabia
[3] KAUST, Phys Sci & Engn PSE Div, Chem Sci Program, Thuwal, Saudi Arabia
关键词
Nickel-zinc alloy; ZnO-ZrO2; Dry reforming of methane (DRM); Deactivation; CO; 2; utilization; NI/ZRO2; CATALYSTS; SUPPORTED NI; CO2; PERFORMANCE; OXYGEN; NICKEL; CARBON; MECHANISM; SURFACE; CH4;
D O I
10.1016/j.jcou.2023.102573
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Stimulated by the capacity of Zn to improve the adoption of CO2 and CH4, we doped a Ni-supported ZrO2 catalyst with Zn to enhance its performance and stability in the dry reforming of methane. We prepared a set of catalysts with different Ni:Zn:Zr proportions and conducted extensive ex situ and in situ characterizations to prove that a Ni-Zn alloy was formed at 750 degrees C under reductive conditions. Combining a tailored morphology of the alloy nanoparticles, strong metal-support (ZnO-ZrO2) interactions, and additional oxygen vacancies created by Zn inclusion resulted in an enhanced catalyst with 15% higher initial activity and higher stability for over 100 h on stream than Zn-free catalyst. Our experimental and modeling results demonstrated that the catalyst with adjusted Ni:Zn:Zr proportion improves the adsorption and reaction rates of CH4 and CO2 while extending its lifetime through enhanced coke precursor gasification compared to its Zn-free counterpart.
引用
收藏
页数:14
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