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https://doi.org/10.1023/A:1014960702381
Title: | Stepwise conversion of methane over supported metal-boron amorphous alloy catalysts | Authors: | Lu, Y. Xiong, Z. Li, J. Lin, J. |
Keywords: | Amorphous alloy catalyst Carbon Higher hydrocarbon formation Hydrogen production Hydrogenation Stepwise conversion of methane |
Issue Date: | Mar-2002 | Citation: | Lu, Y., Xiong, Z., Li, J., Lin, J. (2002-03). Stepwise conversion of methane over supported metal-boron amorphous alloy catalysts. Catalysis Letters 78 (1-4) : 231-237. ScholarBank@NUS Repository. https://doi.org/10.1023/A:1014960702381 | Abstract: | The stepwise conversion of CH4 to higher hydrocarbons over HMCM-22 zeolite supported metal-boron amorphous alloy catalysts has been investigated, including: (1) the influence of metals (Co, Ni, Pt, Rh and Ru) of the catalysts on the reaction; (2) the promotional effect of V on the catalytic behavior of the catalysts; (3) the influence of hydrogenation pressure and CH4 decomposition temperature; and (4) the nature of carbon species. It is found that the yield of C2 + hydrocarbons is strongly dependent on the metals. Good yields of C2 + hydrocarbon are reached only on the supported NiB and CoB catalysts. The probability of C-C chain growth is increased by V promotion without seriously affecting the activities of CH4 decomposition and hydrogenation. The ease of carbon removal via hydrogenation is strongly affected by the CH4 decomposition temperature. Increasing hydrogenation temperature has a negative effect on the yield of C2 + hydrocarbons. XPS measurements show that a carbide-(like) carbon species is active and selective for hydrogenation to produce higher hydrocarbons. Its activity/selectivity is greatly reduced at high CH4 decomposition temperatures, mainly due to transition of the reactive carbidic to un-reactive graphitic form. Graphite/filamental carbons were found to be formed at high CH4 decomposition temperature. | Source Title: | Catalysis Letters | URI: | http://scholarbank.nus.edu.sg/handle/10635/113206 | ISSN: | 1011372X | DOI: | 10.1023/A:1014960702381 |
Appears in Collections: | Staff Publications |
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