Please use this identifier to cite or link to this item: https://doi.org/10.1021/jp401855x
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dc.titleInverse NiAl2O4 on LaAlO3-Al 2O3: Unique catalytic structure for stable CO2 reforming of methane
dc.contributor.authorKathiraser, Y.
dc.contributor.authorThitsartarn, W.
dc.contributor.authorSutthiumporn, K.
dc.contributor.authorKawi, S.
dc.date.accessioned2014-10-09T06:51:56Z
dc.date.available2014-10-09T06:51:56Z
dc.date.issued2013-04-25
dc.identifier.citationKathiraser, Y., Thitsartarn, W., Sutthiumporn, K., Kawi, S. (2013-04-25). Inverse NiAl2O4 on LaAlO3-Al 2O3: Unique catalytic structure for stable CO2 reforming of methane. Journal of Physical Chemistry C 117 (16) : 8120-8130. ScholarBank@NUS Repository. https://doi.org/10.1021/jp401855x
dc.identifier.issn19327447
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/89277
dc.description.abstractNi supported on LaAlO3-Al2O3 (NLA) perovskite oxide was synthesized for syngas production via DRM and compared with Ni supported on γ-Al2O3 (NA) and La 2O3(NL). The formation of LaAlO3 perovskite oxide structure involves interaction with octahedral sites of the alumina support, resulting in the enforced Ni-Al interaction with the underlying tetrahedral Al3+ sites when Ni was impregnated. As a result, the inverse NiAl2O4 spinel structure was formed, and it positively affects the catalytic activity. Catalytic studies show that NLA exhibited the most stable catalytic performance with the lowest carbon deposition. Furthermore, XRD of spent NA catalyst showed phase transformation of support from γ-Al2O3 to α-Al 2O3. Therefore, the enhanced stability of the NLA catalyst throughout the 30 h DRM reaction is attributed to the enhanced lattice stability imparted by the inverse spinel structure and LaAlO3 nanocrystallites on the alumina support, both of which aid in minimizing agglomeration of Ni particles. © 2013 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/jp401855x
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1021/jp401855x
dc.description.sourcetitleJournal of Physical Chemistry C
dc.description.volume117
dc.description.issue16
dc.description.page8120-8130
dc.identifier.isiut000318211200021
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