Zr promotion effect in CO2 methanation over ceria supported nickel catalysts

被引:88
作者
Iglesias, Ignacio [1 ]
Quindimil, Adrian [2 ]
Marino, Fernando [1 ]
De-La-Torre, Unai [2 ]
Gonzalez-Velasco, Juan R. [2 ]
机构
[1] ITHES UBA CONICET, Lab Proc Catalit, Pabellon Ind,Ciudad Univ, RA-1428 Buenos Aires, DF, Argentina
[2] Univ Basque Country UPV EHU, Fac Sci & Technol, Dept Chem Engn, Barrio Sarriena S-N, Leioa 48940, Bizkaia, Spain
关键词
CO2; methanation; Ceria; Doped-ceria; Zirconium; Nickel; NI/CEO2-ZRO2; CATALYSTS; PARTIAL OXIDATION; MIXED OXIDES; SURFACE; CEO2; MECHANISM; POWER; GAS; PR; NANOPARTICLES;
D O I
10.1016/j.ijhydene.2018.11.059
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
Carbon dioxide methanation is an interesting way to reduce greenhouse effect gases emission and, simultaneously, provide a renewable energy source of methane. Ceria and 15 at.% Zr-doped ceria supported nickel catalysts were characterized by means of various techniques (BET, XRD, Raman, H-2-TPR, CO2-TPD, O-2-TPO, OSC and H-2-chemisorption) and evaluated in carbon dioxide methanation. Zr incorporation into catalyst formulation reduced catalysts basicity but favored its reducibility, nickel availability and oxygen storage capacity. These characteristics gave rise to an improved catalytic performance both in terms of activity and stability: temperature required to achieve 50% conversion was reduced in 20 degrees C and low temperature (250 degrees C) stability was improved in around 8%. Initial rates approach was employed to determine reaction rates and apparent activation energies for CO2 methanation, which resulted in 113 and 121 kJ mol(-1) for Ni/CeO2 and Ni/Ce0.85Zr0.15O2, respectively. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1710 / 1719
页数:10
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