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dc.contributor.authorWang, Zhitao
dc.contributor.authorCheng, Yi
dc.contributor.authorShao, Xin
dc.contributor.authorVeder, Jean-Pierre
dc.contributor.authorHu, X.
dc.contributor.authorMa, Y.
dc.contributor.authorWang, J.
dc.contributor.authorXie, K.
dc.contributor.authorDong, Dehua
dc.contributor.authorJiang, San Ping
dc.contributor.authorParkinson, Gordon
dc.contributor.authorBuckley, Craig
dc.contributor.authorLi, Chun-Zhu
dc.date.accessioned2018-12-13T09:12:36Z
dc.date.available2018-12-13T09:12:36Z
dc.date.created2018-12-12T02:46:58Z
dc.date.issued2018
dc.identifier.citationWang, Z. and Cheng, Y. and Shao, X. and Veder, J. and Hu, X. and Ma, Y. and Wang, J. et al. 2018. Nanocatalysts anchored on nanofiber support for high syngas production via methane partial oxidation. Applied Catalysis A: General. 565: pp. 119-126.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/72161
dc.identifier.doi10.1016/j.apcata.2018.08.001
dc.description.abstract

© 2018 Nanofibrous NiAl2O4/Al2O3 ceramic was prepared by electrospinning and subsequent calcination at 1000 °C. Under reducing atmosphere, Ni nanoparticles in situ grew from and were rooted in nanofibrous support. The anchored Ni-NiOx nanocatalysts showed the strong interaction with Al2O3-NiAl2O4 supports owing to the incompletion of NiAl2O4 and NiO reduction and therefore high resistances to aggregation and carbon formation. The nanofibrous catalysts have the advantages of both metal gauze catalysts (fast mass transfer) and supported catalysts (nanosized catalysts). Compared with conventional supported Ni-based catalysts, the nanofibours catalysts produced the highest syngas production during methane partial oxidation at the highest recorded gas hourly space velocity of 8 × 106 L·Kg-1 h-1. The catalytic reaction was operated for 10 h without noticeable performance degradation and the fibrous structure of the nanocatalysts was retained.

dc.titleNanocatalysts anchored on nanofiber support for high syngas production via methane partial oxidation
dc.typeJournal Article
dcterms.source.volume565
dcterms.source.startPage119
dcterms.source.endPage126
dcterms.source.issn0926-860X
dcterms.source.titleApplied Catalysis A: General
curtin.departmentFuels and Energy Technology Institute
curtin.departmentJohn de Laeter Centre
curtin.accessStatusFulltext not available
curtin.facultyScience and Engineering


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