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Tailoring the Product Distribution with Batch and Continuous Process Options in Catalytic Hydrogenation of Furfural
被引:77
作者:
Biradar, Narayan S.
[1
]
Hengne, Amol A.
[1
]
Birajdar, Shobha N.
[1
]
Swami, Rameshwar
[1
]
Rode, Chandrashekhar V.
[1
]
机构:
[1] Natl Chem Lab, CSIR, Chem Engn & Proc Dev Div, Pashan Pune 411008, India
关键词:
PHASE HYDROGENATION;
DIESEL FUEL;
BIOMASS;
CONVERSION;
XYLOSE;
HEMICELLULOSE;
CYCLOHEXANONE;
ALCOHOL;
WASTE;
D O I:
10.1021/op500196x
中图分类号:
O69 [应用化学];
学科分类号:
070301 [无机化学];
摘要:
Various noble metal catalysts were screened in a batch operation for a furfural (FFR) single-step decarbonylation and hydrogenation reaction to obtain THF in high selectivity. Among these, the 3% Pd/C showed complete FFR conversion with a total of 80% selectivity to ring hydrogenated products including tetrahydrofuran (THF). The order of activity exhibited by other noble metals was Pt/C > Re/C > Ru/C. Although Pt/C exhibited the highest activity, its decarbonylation and ring hydrogenation ability were the least (24%) with a major product selectivity of 66% to furfuryl alcohol (FAL). Similarly, the Cu catalyst gave almost complete selectivity to FAL. In a continuous operation (23 g catalyst bed), the 3% Pd/C catalyst showed higher selectivity of >40% compared to THF alone with complete FFR conversion and on-stream activity of similar to 100 h. The reaction pathway elucidated from some control experiments revealed that the decarbonylation of FFR to furan over the Pd/C catalyst is a prerequisite for THF formation.
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页码:1434 / 1442
页数:9
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