Liquid-phase hydrogenation of citral for production of citronellol:: catalyst selection

被引:73
作者
Mäki-Arvela, P
Tiainen, LP
Lindblad, M
Demirkan, K
Kumar, N
Sjöholm, R
Ollonqvist, T
Väyrynen, J
Salmi, T
Murzin, DY [2 ]
机构
[1] Fortum Oil & Gas Oy, Porvoo 06101, Finland
[2] Abo Akad Univ, Proc Chem Grp, Lab Ind Chem, Turku, Finland
[3] Abo Akad Univ, Organ Chem Lab, Turku, Finland
[4] Univ Turku, Dept Appl Phys, Lab Electron Spect & Surface Phys, Turku, Finland
关键词
citral hydrogenation; citronellol; atomic layer epitaxy; Y zeolite; bimetallic catalyst;
D O I
10.1016/S0926-860X(02)00497-0
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
Selective hydrogenation of citral to citronellol has been investigated over Ni supported catalysts. The aim was to compare different support materials and catalyst preparation methods. Selectivity to citronellol was dependent on conversion. The highest maximum selectivity towards citronellol for a Ni/Al2O3 (16.7 wt.% Ni) catalyst at 2.3 bar hydrogen increased from 70% in ethanol to 85% 2-pentanol, where acetalisation could be totally eliminated. In ethanol the highest maximum selectivities to citronellol were about 83% over a 8.8 wt.% Ni/Al2O3 catalyst prepared by atomic layer epitaxy (ALE) method. The lower hydrogenation pressure (2.3 bar) favoured the formation of citronellol compared to results obtained at 5.3 bar hydrogen for all other catalysts, but not for Ni/Al2O3 (16.7 wt.%). Both a bimetallic Ni-Cu/SiO2 (10 wt.% Ni, 3 wt.% Cu) catalyst and a Ni/SiO2 (17.6 wt.% Ni) catalyst prepared by ALE method showed high selectivities to citronellol, 79 and 76%, respectively at 5.3 bar hydrogen. An optimum hydrogenation rate and an optimum specific metal surface area in the catalyst gave the highest selectivities to the desired intermediate, citronellol. Ni supported Y zeolite catalysts were not selective towards formation of citronellol. Instead these catalysts favoured other reactions, like cyclisation, dehydrogenation and cracking. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:271 / 288
页数:18
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