Carbon dioxide reforming of methane over mesoporous Ni/SiO2

Authors
Kim, Dae HanSim, Jong KiLee, JaeyoungSeo, Hyun OokJeong, Myung-GeunKim, Young DokKim, Sang Hoon
Issue Date
2013-10
Publisher
ELSEVIER SCI LTD
Citation
FUEL, v.112, pp.111 - 116
Abstract
Mesoporous SiO2-supported Ni catalyst was fabricated by atomic layer deposition (ALD), and the catalytic activity and stability were investigated in carbon dioxide reforming of methane (CRM) reaction at 800 degrees C. The Ni/SiO2 catalysts showed high initial activity and catalytic stability in the CRM reaction as a result of confinement of Ni particles with a mean size of similar to 10 nm within the pores of SiO2. The Ni particles in pores of mesoporous silica were not only resistant towards sintering but also coke formation during the reaction. In contrast, bare NiO nanoparticles were easily aggregated into larger particles and coke could form under the same reaction conditions, and therefore, much lower reactivity for CRM was found using bare NiO catalysts. It is suggested that Ni particles with very low loading on mesoporous SiO2 could be promising candidate as catalysts of CRM reaction. (C) 2013 Elsevier Ltd. All rights reserved.
Keywords
ATOMIC LAYER DEPOSITION; SYNTHESIS GAS; PALLADIUM CATALYSTS; CO2; REDUCTION; PARTICLES; SYNGAS; SUPPORT; STATE; CH4; ATOMIC LAYER DEPOSITION; SYNTHESIS GAS; PALLADIUM CATALYSTS; CO2; REDUCTION; PARTICLES; SYNGAS; SUPPORT; STATE; CH4; CO2; Ni; Porous silica; Reforming catalyst
ISSN
0016-2361
URI
https://pubs.kist.re.kr/handle/201004/127614
DOI
10.1016/j.fuel.2013.04.089
Appears in Collections:
KIST Article > 2013
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