Highly Selective Continuous Flow Hydrogenation of Cinnamaldehyde to Cinnamyl Alcohol in a Pt/SiO2 Coated Tube Reactor

被引:32
|
作者
Bai, Yang [1 ]
Cherkasov, Nikolay [1 ,2 ]
Huband, Steven [3 ]
Walker, David [3 ]
Walton, Richard I. [4 ]
Rebrov, Evgeny [1 ,2 ,5 ]
机构
[1] Stoli Catalysts Ltd, Coventry CV3 4DS, W Midlands, England
[2] Univ Warwick, Sch Engn, Coventry CV4 7AL, W Midlands, England
[3] Univ Warwick, Dept Phys, Coventry CV4 7AL, W Midlands, England
[4] Univ Warwick, Dept Chem, Coventry CV4 7AL, W Midlands, England
[5] Tver State Tech Univ, Dept Biotechnol & Chem, A Nikitina 22, Tver 170026, Russia
来源
CATALYSTS | 2018年 / 8卷 / 02期
基金
欧洲研究理事会; “创新英国”项目;
关键词
flow chemistry; hydrogenation; unsaturated aldehyde; platinum; tube reactor; alcohol; selectivity; stability; catalyst-coated; SUPPORTED PLATINUM CATALYSTS; LIQUID-PHASE HYDROGENATION; CHEMOSELECTIVE HYDROGENATION; ALPHA; BETA-UNSATURATED ALDEHYDES; ACETYLENE ALCOHOLS; CARBONYL-COMPOUNDS; GAS-LIQUID; ADSORPTION; REDUCTION; PARALLEL;
D O I
10.3390/catal8020058
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A novel continuous flow process for selective hydrogenation of alpha, beta-unsaturated aldehyde (cinnamaldehyde, CAL) to the unsaturated alcohol (cinnamyl alcohol, COL) has been reported in a tube reactor coated with a Pt/SiO2 catalyst. A 90% selectivity towards the unsaturated alcohol was obtained at the aldehyde conversion of 98.8%. This is a six-fold improvement in the selectivity compared to a batch process where acetals were the main reaction products. The increased selectivity in the tube reactor was caused by the suppression of acid sites responsible for the acetal formation after a short period on stream in the continuous process. In a fixed bed reactor, it had a similar acetal suppression phenomenon but showed lower product selectivity of about 47-72% due to mass transfer limitations. A minor change in selectivity and conversion caused by product inhibition was observed during the 110 h on stream with a turnover number (TON) reaching 3000 and an alcohol production throughput of 0.36 kg g(Pt)(-1) day(-1) in the single tube reactor. The catalysts performance after eight reaction cycles was fully restored by calcination in air at 400 degrees C. The tube reactors provide an opportunity for process intensification by increasing the reaction rates by a factor of 2.5 at the reaction temperature of 150 degrees C compared to 90 degrees C with no detrimental effects on catalyst stability or product selectivity.
引用
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页数:18
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