One pot direct catalytic conversion of cellulose to C3 and C4 hydrocarbons using Pt/H-USY zeolite catalyst at low temperature
One-pot direct catalytic conversion of cellulose to light hydrocarbon at low temperature (443K) in the presence of Pt–zeolite catalysts and water was investigated. Results revealed that Pt supported on H+-form ultra stable Y-type (H-USY) zeolite catalyst (Pt/H-USY) enabled direct conversion of cellu...
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Published in | Fuel processing technology Vol. 141; pp. 123 - 129 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
01.01.2016
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Subjects | |
Online Access | Get full text |
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Summary: | One-pot direct catalytic conversion of cellulose to light hydrocarbon at low temperature (443K) in the presence of Pt–zeolite catalysts and water was investigated. Results revealed that Pt supported on H+-form ultra stable Y-type (H-USY) zeolite catalyst (Pt/H-USY) enabled direct conversion of cellulose into C3 and C4 hydrocarbons without hydrogen and other expensive reagents. This production trend is attributable to the bifunctional catalysis of supported Pt and acid site in H-USY zeolite, which has a large pore system and effective acidity. Results revealed that the pre-treatment of catalyst was important for selective olefin production. Air-oxidized Pt/H-USY catalyst showed higher olefin selectivity than the catalyst reduced with hydrogen. The Pt/H-USY catalysts showed high stability under the reaction condition. Results suggest that C5 sugars were the reaction intermediate for the C3 hydrocarbons, and C6 sugars were the intermediate for C4 hydrocarbon formation from cellulose over Pt/H-USY catalysts.
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•Pt/H-USY enabled direct conversion of cellulose into hydrocarbons without hydrogen.•Cellulose was converted to hydrocarbons by the bifunctional catalysis of Pt and H-USY.•Solubilization of cellulose mainly proceeded over acid site of H-USY zeolite.•Cracking of liquiform products into hydrocarbons proceeded over Pt site.•Oxidized Pt/H-USY showed higher olefin selectivity than that of reduced Pt/H-USY. |
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ISSN: | 0378-3820 1873-7188 |
DOI: | 10.1016/j.fuproc.2015.06.032 |