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A continuous process for the glycerolysis of soybean oil
Author(s) -
Noureddini H.,
Harkey D. W.,
Gutsman M. R.
Publication year - 2004
Publication title -
journal of the american oil chemists' society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.512
H-Index - 117
eISSN - 1558-9331
pISSN - 0003-021X
DOI - 10.1007/s11746-004-0882-y
Subject(s) - glycerol , chemistry , soybean oil , mixing (physics) , transesterification , stoichiometry , chromatography , catalysis , molar ratio , chemical engineering , organic chemistry , biochemistry , physics , quantum mechanics , engineering
A continuous process for the glycerolysis of soybean oil with pure and crude glycerol, the co‐product from the transesterification of soybean oil, was investigated in a pilot plant. The process was equipped with a static and a high‐shear mixer. The experimental studies explored the effects of variations in mixing intensity, temperature, reactant flow rates, and reactant stoichiometry on the formation of MG and DG. The developed process resulted in high conversion of TG to MG. The most favorable conditions were 230°C, 40 mL/min total flow, 25 min of reaction time, 2.5∶1 molar ratio of glycerol/soybean oil, and 3600 rpm for the reactions involving crude glycerol where the concentrations of MG and DG in the product were about 56 and 36 wt%, respectively. Under similar conditions, glycerolysis of pure glycerol resulted in 58% MG and 33% DG. In general, higher temperatures and mixing intensities favored the conversion of TG to MG and DG. Reaction temperature had a greater influence on the extent of the reaction than mixing. The formation of MG approached equilibrium for nearly all cases under investigation.