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dc.contributor.authorWang, Y.
dc.contributor.authorSun, J.
dc.contributor.authorZhang, H.
dc.contributor.authorChen, Z.
dc.contributor.authorLin, X.
dc.contributor.authorZhang, Shu
dc.contributor.authorGong, W.
dc.contributor.authorFan, M.
dc.date.accessioned2017-08-24T02:19:15Z
dc.date.available2017-08-24T02:19:15Z
dc.date.created2017-08-23T07:21:49Z
dc.date.issued2015
dc.identifier.citationWang, Y. and Sun, J. and Zhang, H. and Chen, Z. and Lin, X. and Zhang, S. and Gong, W. et al. 2015. In situ catalyzing gas conversion using char as a catalyst/support during brown coal gasification. Energy and Fuels. 29 (3): pp. 1590-1596.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/55522
dc.identifier.doi10.1021/ef502761d
dc.description.abstract

© 2015 American Chemical Society. The purpose of this study was to demonstrate the effectiveness of in situ gas conversion using char as a catalyst/catalyst support in the gasification of Shengli brown coal in an entrained-flow reactor. The catalytic steam gasification of brown coal was also conducted with a feedstock of coal and catalyst mixed under the same conditions. With brown coal char being activated, both calcium and nickel supported on activated char were used as catalysts in these two types of study. The results showed that all catalysts increased H 2 concentrations and had good activity for reforming the gas product from brown coal gasification. As for the effects on promoting H 2 production, the Ca/char and Ni/char catalysts showed higher catalytic activity than char alone in brown coal steam gasification. Physical structure and X-ray diffraction results showed that activated char was a better catalyst carrier, in which O-containing groups played a significant role in syngas reforming, and the disordered structure determined the catalytic activity of the catalyst in the process of brown coal gasification.

dc.publisherAmerican Chemical Society
dc.titleIn situ catalyzing gas conversion using char as a catalyst/support during brown coal gasification
dc.typeJournal Article
dcterms.source.volume29
dcterms.source.number3
dcterms.source.startPage1590
dcterms.source.endPage1596
dcterms.source.issn0887-0624
dcterms.source.titleEnergy and Fuels
curtin.departmentFuels and Energy Technology Institute
curtin.accessStatusFulltext not available


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