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  1. Journal of the American Oil Chemists' Society
  2. Journal of the American Oil Chemists' Society : Volume 74
  3. Journal of the American Oil Chemists' Society : Volume 74, Issue 3, March 1997
  4. Two-phase solvent extraction of canola
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Journal of the American Oil Chemists' Society : Volume 94
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Journal of the American Oil Chemists' Society : Volume 76
Journal of the American Oil Chemists' Society : Volume 75
Journal of the American Oil Chemists' Society : Volume 74
Journal of the American Oil Chemists' Society : Volume 74, Issue 12, December 1997
Journal of the American Oil Chemists' Society : Volume 74, Issue 11, November 1997
Journal of the American Oil Chemists' Society : Volume 74, Issue 10, October 1997
Journal of the American Oil Chemists' Society : Volume 74, Issue 9, September 1997
Journal of the American Oil Chemists' Society : Volume 74, Issue 8, August 1997
Journal of the American Oil Chemists' Society : Volume 74, Issue 7, July 1997
Journal of the American Oil Chemists' Society : Volume 74, Issue 6, June 1997
Journal of the American Oil Chemists' Society : Volume 74, Issue 5, May 1997
Journal of the American Oil Chemists' Society : Volume 74, Issue 4, April 1997
Journal of the American Oil Chemists' Society : Volume 74, Issue 3, March 1997
Use of soy protein concentrates and lecithin products in diets fed to coho and atlantic salmon
Effect of drying methods on molecular properties and functionalities of disulfide bond-cleaved soy proteins
Pilot-scale two-phase extraction of canola
Two-phase solvent extraction of canola
Effects of processing on oxidative stability of sesame oil extracted from intact and dehulled seeds
A bulky phosphite-modified rhodium catalyst for the hydroformylation of unsaturated fatty acid esters
Preparation and characterization of methyl 11-amino-(N-p-toluenesulfonyl)-9-E-octadecenoate and methyl 8-amino-(N-p-toluenesulfonyl)-9-E-octadecenoate
Synthesis of alkyloxy (di)alkylamino propanols, hydroxy alkyloxy (di)alkylamino propanols, and the dimer compounds for use as fuel additives
Synthesis of derivatives of alkylamino alkyloxy propanol structures by N-alkylation, acylation, and nitration. Application as fuel additives
Estolide production with modified clay catalysts and process conditions
Lipase PS-catalyzed transesterification of citronellyl butyrate and geranyl caproate: Effect of reaction parameters
Enzymatic synthesis of estolides by a bioreactor
Enzymatic modification of triolein: Incorporation of caproic and butyric acids to produce reduced-calorie structured lipids
Nondestructive single-seed oil determination of meadowfoam by near-infrared transmission spectroscopy
Analysis of seed oil from ricinus communis and dimorphoteca pluvialis by gas and supercritical fluid chromatography
A method for determining kernel moisture content and aflatoxin concentrations in peanuts
Diffuse reflectance fourier transform infrared spectroscopy of triacylglycerol and oleic acid adsorption on synthetic magnesium silicate
Effect of fatty acid composition of phospholipids on their antioxidant properties and activity index
Oxidative stabilities of soybean oils with elevated palmitate and reduced linolenate contents
Identification and function of antioxidants from oat groats and hulls
Determination of environmentally relevant physical-chemical properties of some fatty acid esters
Regular-sized cell creation in microchannel emulsification by visual microprocessing method
Stability of furanoid fatty acids in soybean oil
Effect of interesterification on the structure and physical properties of high-stearic acid soybean oils
Comparison of rancimat evaluation modes to assess oxidative stability of fish oils
Journal of the American Oil Chemists' Society : Volume 74, Issue 2, February 1997
Journal of the American Oil Chemists' Society : Volume 74, Issue 1, January 1997

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Two-phase solvent extraction of canola

Content Provider Springer Nature Link
Author Thobani, Mahmood Diosady, Levente L.
Copyright Year 1997
Abstract The equilibrium relationships in the extraction process that was developed in our research laboratory for the treatment of canola were studied. In the process, hexane is used as well as CH$_{3}$OH that contains 5% (vol/vol) H$_{2}$O and 0.08% (w/w) NaOH to simultaneously produce improved meal and high-quality oil. Equilibrium data for canola oil in the hexane-CH$_{3}$OH/H$_{2}$o/NaOH, meal-hexane, and meal-CH$_{3}$OH/H$_{2}$O/NaOH-hexane systems are reported. A high partition coefficient for oil between hexane and the polar phase provided a large driving force for mass transfer. The presence of the CH$_{3}$OH phase improved oil extraction, probably by rupturing the cell structure. The process proved to be a somewhat less desirable replacement for CH$_{3}$OH/H$_{2}$O/NH$_{3}$ extraction and recovered 93.5% of the oil and 91.8% of the protein in the seed, while with CH$_{3}$OH/H$_{2}$O/NH$_{3}$, the oil and protein recoveries were 96.8 and 94.0%, respectively. The NaOH treatment removed only 50.2% of the glucosinolates, and some of the oil was hydrolyzed by the NaOH, making the process less effective, despite its simplicity.
Starting Page 207
Ending Page 214
Page Count 8
File Format PDF
ISSN 0003021X
Journal Journal of the American Oil Chemists' Society
Volume Number 74
Issue Number 3
e-ISSN 15589331
Language English
Publisher Springer-Verlag
Publisher Date 1997-01-01
Publisher Place Berlin, Heidelberg
Access Restriction One Nation One Subscription (ONOS)
Subject Keyword Canola meal canola oil canola seed extraction glucosinolates oil equilibrium Industrial Chemistry/Chemical Engineering Analytical Chemistry Chemistry/Food Science Biotechnology Biomaterials Agriculture
Content Type Text
Resource Type Article
Subject Organic Chemistry Chemical Engineering
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