Essential Role of the Support for Nickel-Based CO2 Methanation Catalysts

被引:261
作者
Shen, Liang [1 ]
Xu, Jing [1 ]
Zhu, Minghui [1 ]
Han, Yi-Fan [1 ]
机构
[1] East China Univ Sci & Technol, Sch Chem Engn, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
关键词
support; CO2; methanation; heterogeneous catalysis; metal-support interaction; MESOSTRUCTURED SILICA NANOPARTICLES; HYDROTALCITE-DERIVED CATALYST; NI-BASED CATALYST; LOW-TEMPERATURE; CARBON-DIOXIDE; NI/GAMMA-AL2O3; CATALYSTS; HYDROGENATION SELECTIVITY; THERMODYNAMIC ANALYSIS; NI/ZRO2; ENHANCED ACTIVITY;
D O I
10.1021/acscatal.0c03471
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 carbon dioxide (CO2) methanation reaction not only provides a solution for mitigating the excessive carbon dioxide emissions but also can potentially be employed for the storage and transportation of low-grade energies. A supported nickel-based catalyst is the most promising candidate for the CO2 methanation reaction. Additionally, understanding the role of the support is essential for the rational design of nickel-based CO2 methanation catalysts. Herein, we elaborated on the effect of the support on the catalyst structure, CO2 adsorption, CO2 activation, methanation mechanism, and deactivation process. Future directions are suggested to elucidate the fundamental aspects of this catalytic system, including the formation mechanism of preferentially exposed facets, the nature of strong metal-support interactions, the balance between support reducibility and basicity, and the CO2 methanation pathways over nickel-based catalysts with various supports.
引用
收藏
页码:14581 / 14591
页数:11
相关论文
共 121 条
[1]   CO HYDROGENATION ON A NICKEL-CATALYST .1. KINETICS AND MODELING OF A LOW-TEMPERATURE SINTERING PROCESS [J].
AGNELLI, M ;
KOLB, M ;
MIRODATOS, C .
JOURNAL OF CATALYSIS, 1994, 148 (01) :9-21
[2]  
Agrawal PK., 1980, CATALYST DEACTIVATIO, V6, P179
[3]   Synthesis of lanthanide series (La, Ce, Pr, Eu & Gd) promoted Ni/γ-Al2O3 catalysts for methanation of CO2 at low temperature under atmospheric pressure [J].
Ahmad, Waciar ;
Younis, Muhammad Naeem ;
Shawabkeh, Reyad ;
Ahmed, Shakeel .
CATALYSIS COMMUNICATIONS, 2017, 100 :121-126
[4]   Higher tolerance to sulfur poisoning in CO2 methanation by the presence of CeO2 [J].
Alarcon, Andreina ;
Guilera, Jordi ;
Soto, Rodrigo ;
Andreu, Teresa .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2020, 263
[5]   Catalytic CO2 valorization into CH4 on Ni-based ceria-zirconia. Reaction mechanism by operando IR spectroscopy [J].
Aldana, P. A. Ussa ;
Ocampo, F. ;
Kobl, K. ;
Louis, B. ;
Thibault-Starzyk, F. ;
Daturi, M. ;
Bazin, P. ;
Thomas, S. ;
Roger, A. C. .
CATALYSIS TODAY, 2013, 215 :201-207
[6]   CO2, the greenhouse effect and global warming: from the pioneering work of Arrhenius and Callendar to today's Earth System Models [J].
Anderson, Thomas R. ;
Hawkins, Ed ;
Jones, Philip D. .
ENDEAVOUR, 2016, 40 (03) :178-187
[7]  
[Anonymous], [No title captured]
[8]   Enhanced activity of CO2 methanation over Ni/CeO2-ZrO2 catalysts: Influence of preparation methods [J].
Ashok, J. ;
Ang, M. L. ;
Kawi, S. .
CATALYSIS TODAY, 2017, 281 :304-311
[9]   CO2 methanation over heterogeneous catalysts: recent progress and future prospects [J].
Aziz, M. A. A. ;
Jalil, A. A. ;
Triwahyono, S. ;
Ahmad, A. .
GREEN CHEMISTRY, 2015, 17 (05) :2647-2663
[10]   CO2 methanation over Ni-promoted mesostructured silica nanoparticles: Influence of Ni loading and water vapor on activity and response surface methodology studies [J].
Aziz, M. A. A. ;
Jalil, A. A. ;
Triwahyono, S. ;
Saad, M. W. A. .
CHEMICAL ENGINEERING JOURNAL, 2015, 260 :757-764