Tailoring the Product Distribution with Batch and Continuous Process Options in Catalytic Hydrogenation of Furfural

被引:63
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
081704 ;
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.
引用
收藏
页码:1434 / 1442
页数:9
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