Mo2C catalyzed vapor phase hydrodeoxygenation of lignin-derived phenolic compound mixtures to aromatics under ambient pressure
被引:105
作者:
Chen, Cha-Jung
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Univ Minnesota Twin Cities, Dept Chem Engn & Mat Sci, 421 Washington Ave SE, Minneapolis, MN 55455 USAUniv Minnesota Twin Cities, Dept Chem Engn & Mat Sci, 421 Washington Ave SE, Minneapolis, MN 55455 USA
Chen, Cha-Jung
[1
]
Lee, Wen-Sheng
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Univ Minnesota Twin Cities, Dept Chem Engn & Mat Sci, 421 Washington Ave SE, Minneapolis, MN 55455 USA
Dow Chem Co USA, Core R&D, 2030 Dow Ctr, Midland, MI 48674 USAUniv Minnesota Twin Cities, Dept Chem Engn & Mat Sci, 421 Washington Ave SE, Minneapolis, MN 55455 USA
Lee, Wen-Sheng
[1
,2
]
Bhan, Aditya
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Univ Minnesota Twin Cities, Dept Chem Engn & Mat Sci, 421 Washington Ave SE, Minneapolis, MN 55455 USAUniv Minnesota Twin Cities, Dept Chem Engn & Mat Sci, 421 Washington Ave SE, Minneapolis, MN 55455 USA
Bhan, Aditya
[1
]
机构:
[1] Univ Minnesota Twin Cities, Dept Chem Engn & Mat Sci, 421 Washington Ave SE, Minneapolis, MN 55455 USA
[2] Dow Chem Co USA, Core R&D, 2030 Dow Ctr, Midland, MI 48674 USA
High aromatics yield (> 90%, benzene and toluene) was obtained from vapor phase hydrodeoxygenation (HDO) of phenolic compound mixtures containing m-cresol, anisole, 1,2-dimethoxybenzene, and guaiacol over molybdenum carbide catalysts (Mo2C) under atmospheric pressure at 533-553 K, even with H-2 to phenolic compound molar ratios of similar to 3,300. Toluene selectivity increased proportionately (4%-66%) to m-cresol content in HDO of phenolic compound mixtures (molar composition: 0%-70%) at quantitative conversion. Phenol selectivity increased with decreasing conversion, implying that the aryl-methoxyl bond in guaiacol is cleaved first, before the aryl-hydroxyl bond. Low selectivity to cyclohexane and methylcyclohexane (< 10%) across the conversions investigated (18-94%) demonstrates that undesired successive hydrogenation reactions of aromatics over Mo2C were inhibited, presumably due to in situ oxygen modification, as inferred from titration studies of aromatic hydrogenation reactions using methanol and water as titrants. (C) 2015 Elsevier B.V. All rights reserved.
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UNIV LOUIS PASTEUR,EHICS,CHIM MAT CATALYT LAB,1 RUE BLAISE PASCAL,F-67000 STRASBOURG,FRANCEUNIV LOUIS PASTEUR,EHICS,CHIM MAT CATALYT LAB,1 RUE BLAISE PASCAL,F-67000 STRASBOURG,FRANCE
CUONG, PH
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LEDOUX, MJ
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UNIV LOUIS PASTEUR,EHICS,CHIM MAT CATALYT LAB,1 RUE BLAISE PASCAL,F-67000 STRASBOURG,FRANCEUNIV LOUIS PASTEUR,EHICS,CHIM MAT CATALYT LAB,1 RUE BLAISE PASCAL,F-67000 STRASBOURG,FRANCE
LEDOUX, MJ
;
GUILLE, J
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UNIV LOUIS PASTEUR,EHICS,CHIM MAT CATALYT LAB,1 RUE BLAISE PASCAL,F-67000 STRASBOURG,FRANCEUNIV LOUIS PASTEUR,EHICS,CHIM MAT CATALYT LAB,1 RUE BLAISE PASCAL,F-67000 STRASBOURG,FRANCE
机构:
Univ Paris 06, CNRS, Lab React Surface, UMR 7609, F-75252 Paris 05, FranceUniv Paris 06, CNRS, Lab React Surface, UMR 7609, F-75252 Paris 05, France
Choi, JS
;
Bugli, G
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Univ Paris 06, CNRS, Lab React Surface, UMR 7609, F-75252 Paris 05, FranceUniv Paris 06, CNRS, Lab React Surface, UMR 7609, F-75252 Paris 05, France
Bugli, G
;
Djéga-Mariadassou, G
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Univ Paris 06, CNRS, Lab React Surface, UMR 7609, F-75252 Paris 05, FranceUniv Paris 06, CNRS, Lab React Surface, UMR 7609, F-75252 Paris 05, France
机构:
UNIV LOUIS PASTEUR,EHICS,CHIM MAT CATALYT LAB,1 RUE BLAISE PASCAL,F-67000 STRASBOURG,FRANCEUNIV LOUIS PASTEUR,EHICS,CHIM MAT CATALYT LAB,1 RUE BLAISE PASCAL,F-67000 STRASBOURG,FRANCE
CUONG, PH
;
LEDOUX, MJ
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机构:
UNIV LOUIS PASTEUR,EHICS,CHIM MAT CATALYT LAB,1 RUE BLAISE PASCAL,F-67000 STRASBOURG,FRANCEUNIV LOUIS PASTEUR,EHICS,CHIM MAT CATALYT LAB,1 RUE BLAISE PASCAL,F-67000 STRASBOURG,FRANCE
LEDOUX, MJ
;
GUILLE, J
论文数: 0引用数: 0
h-index: 0
机构:
UNIV LOUIS PASTEUR,EHICS,CHIM MAT CATALYT LAB,1 RUE BLAISE PASCAL,F-67000 STRASBOURG,FRANCEUNIV LOUIS PASTEUR,EHICS,CHIM MAT CATALYT LAB,1 RUE BLAISE PASCAL,F-67000 STRASBOURG,FRANCE
机构:
Univ Paris 06, CNRS, Lab React Surface, UMR 7609, F-75252 Paris 05, FranceUniv Paris 06, CNRS, Lab React Surface, UMR 7609, F-75252 Paris 05, France
Choi, JS
;
Bugli, G
论文数: 0引用数: 0
h-index: 0
机构:
Univ Paris 06, CNRS, Lab React Surface, UMR 7609, F-75252 Paris 05, FranceUniv Paris 06, CNRS, Lab React Surface, UMR 7609, F-75252 Paris 05, France
Bugli, G
;
Djéga-Mariadassou, G
论文数: 0引用数: 0
h-index: 0
机构:
Univ Paris 06, CNRS, Lab React Surface, UMR 7609, F-75252 Paris 05, FranceUniv Paris 06, CNRS, Lab React Surface, UMR 7609, F-75252 Paris 05, France