A new heterogeneously catalytic pathway for isomerization of linoleic acid over Ru/C and Ni/H-MCM-41 catalysts

被引:56
作者
Bernas, A
Laukkanen, P
Kumar, N
Mäki-Arvela, P
Väyrynen, J
Laine, E
Holmbom, B
Salmi, T
Murzin, DY [1 ]
机构
[1] Abo Akad Univ, Proc Chem Grp, Lab Ind Chem, FIN-20500 Turku, Finland
[2] Univ Turku, Dept Phys, Surface Phys Lab, FIN-20014 Turku, Finland
[3] Univ Turku, Dept Phys, Lab Ind Phys, FIN-20014 Turku, Finland
[4] Abo Akad Univ, Wood Chem Lab, Proc Chem Grp, FIN-20500 Turku, Finland
关键词
functional food; conjugated linoleic acids; Ni/HMCM-41; double-bond migration; isomerization; hydrogenation;
D O I
10.1006/jcat.2002.3690
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
The isomerization reaction of linoleic acid (cis-9,cis-12-octadecadienoic acid) to conjugated linoleic acids (CLA) was studied. A new heterogeneously catalytic pathway was developed for synthesis of CLA at mild reaction conditions (80-120degreesC) over Ru/C and Ni/H-MCM-41 catalysts in a diluted system. The isomerization reaction was tested in 1-octanol and n-decane. Solvents with low polarity were selected to afford good reactant adsorption on the catalyst surface and a high solvent-to-reactant ratio was used to prevent potential side reactions. Catalyst characterization was done by X-ray powder diffraction, X-ray fluorescence, X-ray photoelectron spectroscopy, hydrogen temperature-programmed desorption, direct current plasma atomic emission spectrometry, and BET techniques. The reactions taking place were isomerization of linoleic acid C-18:2, hydrogenation of C-18:2 acids to C-18:1 monounsaturated octadecenoic acids (oleic acid, elaidic acid, cis-vaccenic acid and trans-vaccenic acid), and further hydrogenation of C-18:1 acids to C-18:0 stearic acid (n-octadecanoic acid) where isomerization and hydrogenation were two competing parallel reactions. The isomerization reaction was enhanced by preactivation of the catalysts under hydrogen, but such a treatment also increased the side reaction double-bond hydrogenation. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:354 / 366
页数:13
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