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1.
《Fuel Processing Technology》2005,86(10):1059-1070
Biodiesel, defined as the mono-alkyl esters of vegetable oils or animal fats, is an “alternative” diesel fuel that is becoming accepted in a steadily growing number of countries around the world. Since the source of biodiesel varies with the location and other sources such as recycled oils are continuously gaining interest, it is important to possess data on how the various fatty acid profiles of the different sources can influence biodiesel fuel properties. The properties of the various individual fatty esters that comprise biodiesel determine the overall fuel properties of the biodiesel fuel. In turn, the properties of the various fatty esters are determined by the structural features of the fatty acid and the alcohol moieties that comprise a fatty ester. Structural features that influence the physical and fuel properties of a fatty ester molecule are chain length, degree of unsaturation, and branching of the chain. Important fuel properties of biodiesel that are influenced by the fatty acid profile and, in turn, by the structural features of the various fatty esters are cetane number and ultimately exhaust emissions, heat of combustion, cold flow, oxidative stability, viscosity, and lubricity. 相似文献
2.
Mixed Alkyl Esters from Cottonseed Oil: Improved Biodiesel Properties and Blends with Diesel Fuel 总被引:1,自引:0,他引:1
Hem Joshi Bryan R. Moser Terry Walker 《Journal of the American Oil Chemists' Society》2012,89(1):145-153
Transesterification of refined cottonseed oil (CSO) was carried out with methanol, ethanol, 1-butanol, and various mixtures
of these alcohols to produce biodiesel. In the mixed alcohol transesterifications, formation of methyl esters was favored
over ethyl and butyl esters. The influence of ester head group on fuel properties was determined. Specifically, cold flow
properties, lubricity, and energy content improved in the order: CSO butyl esters (CSBE, best) > ethyl esters (CSEE) > methyl
esters (CSME). Higher kinematic viscosities (KVs) as well as lower iodine values (IVs) and wear scars were observed with larger
ester head groups. Blends of CSME, CSEE and CSBE exhibited properties intermediate to the neat esters. All ester samples were
within the limits prescribed in ASTM D6751 and EN 14214 for cetane number, acid value (AV), glycerol (free and total) content,
sulfur, and phosphorous. Also examined was the influence of blending alkyl esters with petrodiesel. All blends exhibited improved
cold flow properties versus unblended alkyl esters. Enhanced lubricity was observed after blending. With increasing content
of biodiesel, higher KVs and lower energy contents were observed. Finally, all blends were within the limits specified in
ASTM D975 and D7467 for AV, KV and sulfur. 相似文献
3.
Nikolaos B. Kyriakidis Theophanis Katsiloulis 《Journal of the American Oil Chemists' Society》2000,77(12):1235-1238
A new calculation method for the determination of iodine value (IV) from measurements of fatty acid methyl esters is proposed.
The method is based on the quantitative determination of fatty acid methyl esters of vegetable oils by capillary gas chromatography.
IV is a measure of the number of double bonds in the unsaturated fatty acids in one gram of oil. The analytical methodology
of its evaluation includes the use of rather health dangerous reagents, and for that reason is mostly avoided by laboratory
analysts. A calculation procedure to determine the IV of oils from their fatty acid methyl ester composition is in use based
on the American Oil Chemists’ Society (AOCS) method Cd 1c-85. A new calculation procedure for IV, based also on the evaluation
of the fatty acid methyl esters of oils, was developed. The application of the proposed calculation methodology was checked
with olive oil, corn oil, soybean oil, cottonseed oil, and sunflower seed oil. The proposed calculation gave results in better
agreement with the Wijs method than with the relevant AOCS method. 相似文献
4.
Titipong Issariyakul Mangesh G. Kulkarni Lekha C. Meher Ajay K. Dalai Narendra N. Bakhshi 《Chemical engineering journal (Lausanne, Switzerland : 1996)》2008,140(1-3):77-85
Used cooking oil (UCO) was mixed with canola oil at various ratios in order to make use of used cooking oil for production of biodiesel and also lower the cost of biodiesel production. Methyl and ethyl esters were prepared by means of KOH-catalyzed transesterification from the mixtures of both the oils. Water content, acid value and viscosity of most esters met ASTM standard except for ethyl esters prepared from used cooking oil. Canola oil content of at least 60% in the used cooking oil/canola oil feedstock is required in order to produce ethyl ester satisfying ASTM specifications. Although ethanolysis was proved to be more challenging, ethyl esters showed reduced crystallization temperature (−45.0 to −54.4 °C) as compared to methyl esters (−35.3 to −43.0 °C). A somewhat better low-temperature property of ester was observed at higher used cooking oil to canola oil ratio in spite of similar fatty acid compositions of both oils. 相似文献
5.
Thomas K. Miwa 《Journal of the American Oil Chemists' Society》1971,48(6):259-264
HCl-catalyzed ethanolysis followed by saponification readily surmounts the resistance of long chain wax esters to direct hydrolysis
by alkali. Additionally, choosing ethyl instead of methyl esters allows baseline separations between long-chain alcohols and
corresponding esters in gas liquid chromatographic (GLC) analysis of total alcohol and acid components before saponification.
Liquid wax esters were analyzed on a temperature-programmed 3% OV-1 silicone column. Geographical and genetic effects on the
variability of jojoba oil composition were investigated with five different seed samples. Major constituents in jojoba seed
oil from shrubs in the Arizona deserts, as indicated by GLC analyses of oil, ethanolysis product, isolated fatty alcohols
and methyl esters of isolated fatty acids, were C40 wax ester 30%, C42 wax ester 50% and C44 wax ester 10%; octadecenoic acid 6%; eicosenoic acid 35%, docosenoic acid 7%, eicosenol 22%, docosenol 21% and tetracosenol
4%. Oil from smaller leaved prostrate plants growing along California’s oceanside showed a slight tendency toward higher molecular
size than oils from the California desert and Arizona specimens. The wax esters are made up of a dispro-portionately large
amount of docosenyl eicosenoate and are not a random combination of constituent acids and alcohols.Lunaria annua synthetic wax ester oil was used as a model for evaluating the analytical procedures.
Presented at the AOCS Meeting, Chicago, September 1970
No. Utiliz, Res. Dev. Div., ARS, USDA. 相似文献
6.
Methyl esters of commercial grades of lauric, myristic, palmitic, stearic, linoleic and linolenic acids, as well as ethyl and butyl esters of oleic acid, were burned in a diesel engine to determine their efficiencies as fuels. Triolein and some common vegetable oils were burned as comparison fuels and No. 2 diesel fuel was used as a control. The fuels were tested in a single-cylinder direct-injection engine running at rated speed and load in short-term, performance engine tests. Specific fuel consumption and thermal efficiencies of the engine burning these fuels were then determined. Among the methyl esters of the saturated acids, thermal efficiency was inversely related to chain length of the fatty acid. Introduction of a double bond resulted in increased efficiency. Further increases in unsaturation had negligible effects on thermal efficiencies. Ethyl oleate had the highest thermal efficiency and butyl oleate had the lowest thermal efficiency of any of the ester fuels tested. Most of the ester fuels produced higher thermal efficiencies than did No. 2 diesel fuel. Triolein produced the lowest specific fuel consumption of the triglyceride fuels and peanut oil produced the lowest specific fuel consumption of the vegetable oils. The data suggest that ethyl esters of monounsaturated or short-chain fatty acids should make good alternative fuels and that they should be further evaluated in longterm engine tests. 相似文献
7.
衍生于植物油和动物脂肪的生物质油是生物润滑油的重要原料。与矿物油相比,生物质油具有低毒性、高生物降解性、高润滑性和良好的黏温性等优点,但其含双键和甘油酯基导致低温流动性和氧化稳定性差。因此,生物质油不宜直接作为润滑油基础油使用。生物质油经环氧化改性增加了氧化稳定性,加强了对金属表面的吸附,提高了润滑性。但是,单纯进行环氧化改性,也会导致油品的黏温性和低温流动性变差。因此,需要对环氧生物质油进一步开环改性。对比选择性氢化、异构化等改性方法,环氧化-开环方法反应条件温和,分子设计空间大。本文总结了由环氧植物油通过开环醚构化、酰化合成生物基础油的现状和发展趋势, 重点阐述了环氧植物油及其衍生物环氧脂肪酸甲酯与有机醇、羧酸和酸酐合成润滑油的研究进展,分析了改性分子结构对润滑油性能的影响,讨论了合成生物润滑油研究中尚存的问题, 并认为优化改性工艺、开发绿色高效的催化剂是未来的发展方向。 相似文献
8.
Variables affecting the yields of fatty esters from transesterified vegetable oils 总被引:47,自引:25,他引:47
B. Freedman E. H. Pryde T. L. Mounts 《Journal of the American Oil Chemists' Society》1984,61(10):1638-1643
Transesterification reaction variables that affect yield and purity of the product esters from cottonseed, peanut, soybean
and sunflower oils include molar ratio of alcohol to vegetable oil, type of catalyst (alkaline vs acidic), temperature and
degree of refinement of the vegetable oil. With alkaline catalysts (either sodium hydroxide or methoxide), temperatures of
60 C or higher, molar ratios of at least 6 to 1 and with fully refined oils, conversion to methyl, ethyl and butyl esters
was essentially complete in 1 hr. At moderate temperatures (32 C), vegetable oils were 99% transesterified in ca. 4 hr with
an alkaline catalyst. Transesterification by acid catalysis was much slower than by alkali catalysis. Although the crude oils
could be transesterified, ester yields were reduced because of gums and extraneous material present in the crude oils.
Presented at the American Oil Chemists’ Society annual meeting, Chicago, May 1983. 相似文献
9.
Phattaraporn Kaewkool Kanisa Kittiratanapiboon Kornkanok Aryusuk Kanit Krisnangkura 《European Journal of Lipid Science and Technology》2009,111(5):474-480
The fatty acid compositions of vegetable or other plant seed oils are generally determined by gas chromatography (GC). Methyl esters (the most volatile derivatives) are the preferred derivatives for GC analysis. Esters of higher alcohols are good for the separation of volatile and positional isomers. All the esters of the C1–C8 alcohols of vegetable oils were silmilarly prepared by passing the reaction mixture containing the desired alcohol, oil and tetrahydrofuran through the micro‐reactor (a 3‐mL dispossible syringe packed with 0.5 g of NaOH powder). The reaction products were acidified with acetic acid and the mixture was analyzed by high‐performance size exclusion chromatography and GC. Transesterification was quantitative for primary alcohols, but an appreciable amount of free fatty acids was formed for secondary alcohols. Coriander seed oil was quantitatively esterified with 2‐ethyl 1‐hexanol with the micro‐reactor in less than 1 min. Oleic and petroselinic acid 2‐ethyl 1‐hexyl esters are baseline separated on an Rtx‐2330 capillary column (30 m×0.25 mm, 0.25 µm film thickness). 相似文献
10.
Cheng-Jung Tsai Chih-Cheng Liu Lang-Bang Hung Bonnie Sun Pan 《Journal of the American Oil Chemists' Society》2012,89(1):9-16
Tetramethylammonium hydroxide (TMAH)-catalyzed transesterification was developed as a rapid and reliable method using gas
chromatography (GC) to determine the total fatty acid profile and to quantify the ethyl esters of eicosapentaenoic acid (EPA)
and docosahexaenoic acid (DHA) in 20 brands of encapsulated fish oil products. The AOAC method with boron trifluoride (BF3) as a catalyst was used as a reference. After the respective transesterifications of BF3 and TMAH, seven brands of encapsulated fish oil showed a single peak of EPA or DHA in the chromatograms, while 13 brands
showed a single peak in the chromatograms after BF3 esterification, but doublet peaks of EPA or DHA after TMAH esterification. By comparing with the GC/MS NIST library and authentic
standard fatty acids of ethyl esters, the two pairs of doublet peaks were confirmed the ethyl and methyl esters of EPA and
DHA, while the sum of the peak areas of the doublet represented the content of EPA or DHA. The reaction time course concluded
that optimal TMAH transesterification was obtained at 25 °C for 10 min and using GC columns of low to medium polarity including
Rtx-wax and Rtx-2330 were able to differentiate and quantify the ethyl- and methyl-esterified EPA and DHA, while RT-2560 column
with higher polarity than the two other columns was unable to resolve the ethyl ester from the methyl ester of EPA or DHA.
An EPA/DHA ratio of ≥1.10 may serve as an indicator of fish oil fortified with the ethyl ester of EPA. 相似文献
11.
Pascale Sabin Bouchra Benjelloun-Mlayah Michel Delmas 《Journal of the American Oil Chemists' Society》1997,74(10):1227-1233
Two sets of variable oil length, alkyd resins modified by sunflower oil (SOA) and by rapeseed oil (ROA), were evaluated in
offset formulations with mineral oils as diluent. The more suitable alkyds for this kind of application were determined. In
a second experiment, hydrocarbon solvents were substituted by the fatty acid methyl esters derived from rapeseed oil or sunflower
oil to produce ecologically friendly offset printing inks. Finally, the ROA and the SOA were associated with the methyl esters
derived from the same vegetable oil. New properties of the varnishes composed of a vegetable diluent were evaluated. The quickset
formulations with the methyl esters do not need important modifications, as opposed to the heatset formulations. 相似文献
12.
《Fuel Processing Technology》2005,86(10):1087-1096
Semirefined and refined vegetable oils are the predominant feedstocks for the production of biodiesel. However, their relatively high costs render the resulting fuels unable to compete with petroleum-derived fuel. We have investigated the production of fatty acid methyl esters (FAME; biodiesel) from soapstock (SS), a byproduct of edible oil refining that is substantially less expensive than edible-grade refined oils. Multiple approaches were taken in search of a route to the production of fatty acid methyl esters from soybean soapstock. The most effective method involved the complete saponification of the soapstock followed by acidulation using methods similar to those presently employed in industry. This resulted in an acid oil with a free fatty acid (FFA) content greater than 90%. These fatty acids were efficiently converted to methyl esters by acid-catalyzed esterification. The fatty acid composition of the resulting ester product reflected that of soy soapstock and was largely similar to that of soybean oil. Following a simple washing protocol, this preparation met the established specifications for biodiesel of the American Society for Testing and Materials. Engine emissions and performance during operation on soy soapstock biodiesel were comparable to those on biodiesel from soy oil. An economic analysis suggested that the production cost of soapstock biodiesel would be approximately US$ 0.41/l, a 25% reduction relative to the estimated cost of biodiesel produced from soy oil. 相似文献
13.
Bryan R. Moser Michael J. Haas Jill K. Winkler Michael A. Jackson Sevim Z. Erhan Gary R. List 《European Journal of Lipid Science and Technology》2007,109(1):17-24
Biodiesel, an alternative fuel derived from vegetable oils or animal fats, continues to undergo rapid worldwide growth. Specifications mandating biodiesel quality, most notably in Europe (EN 14214) and the USA (ASTM D6751), have emerged that limit feedstock choice in the production of biodiesel fuel. For instance, EN 14214 contains a specification for iodine value (IV; 120 g I2/100 g maximum) that eliminates soybean oil as a potential feedstock, as it generally has an IV >120. Therefore, partially hydrogenated soybean oil methyl esters (PHSME; IV = 116) were evaluated as biodiesel by measuring a number of fuel properties, such as oxidative stability, low‐temperature performance, lubricity, kinematic viscosity, and specific gravity. Compared to soybean oil methyl esters (SME), PHSME were found to have superior oxidative stability, similar specific gravity, but inferior low‐temperature performance, kinematic viscosity, and lubricity. The kinematic viscosity and lubricity of PHSME, however, were within the prescribed US and European limits. There is no universal value for low‐temperature performance in biodiesel specifications, but PHSME have superior cold flow behavior when compared to other alternative feedstock fuels, such as palm oil, tallow and grease methyl esters. The production of PHSME from refined soybean oil would increase biodiesel production costs by US$ 0.04/L (US$ 0.15/gal) in comparison to SME. In summary, PHSME are within both the European and American standards for all properties measured in this study and deserve consideration as a potential biodiesel fuel. 相似文献
14.
Esters from vegetable oils have attracted a great deal of interest as substitutes for petrodiesel to reduce dependence on imported petroleum and provide a fuel with more benign environmental properties. In this work biodiesel was prepared from cottonseed oil by transesterification with methanol, using sodium hydroxide, potassium hydroxide, sodium methoxide and potassium methoxide as catalysts. A series of experiments were conducted in order to evaluate the effects of reaction variables such as methanol/oil molar ratio (3:1–15:1), catalyst concentration (0.25–1.50%), temperature (25–65 °C), and stirring intensity (180–600 rpm) to achieve the maximum yield and quality. The optimized variables of 6:1 methanol/oil molar ratio (mol/mol), 0.75% sodium methoxide concentration (wt.%), 65 °C reaction temperature, 600 rpm agitation speed and 90 min reaction time offered the maximum methyl ester yield (96.9%). The obtained fatty acid methyl esters (FAME) were analyzed by gas chromatography (GC) and 1H NMR spectroscopy. The fuel properties of cottonseed oil methyl esters (COME), cetane number, kinematic viscosity, oxidative stability, lubricity, cloud point, pour point, cold filter plugging point, flash point, ash content, sulfur content, acid value, copper strip corrosion value, density, higher heating value, methanol content, free and bound glycerol were determined and are discussed in the light of biodiesel standards such as ASTM D6751 and EN 14214. 相似文献
15.
Isolation of Non-methylene Interrupted or Acetylenic Fatty Acids from Seed Oils Using Semi-preparative Supercritical Chromatography
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Fernando Montañés Stephen Tallon Owen Catchpole 《Journal of the American Oil Chemists' Society》2017,94(7):981-991
Preparative scale supercritical fluid chromatography was used for isolating and purifying uncommon non-methylene interrupted or acetylenic polyunsaturated fatty acids ethyl esters from seed oils. Fractionation of Biota orientalis seed oil ethyl esters was performed by supercritical fluid chromatography to obtain juniperonic acid [(5Z,11Z,14Z,17Z)-eicosa-5,11,14,17-tetraenoic acid], a non-methylene interrupted polyunsaturated fatty acid. Fractionation of sandalwood seed oil ethyl esters yielded ximenynic acid [(E)-octadec-11-en-9-ynoic acid], an acetylenic polyunsaturated fatty acid. The effects of CO2 flow rate, column stationary phase and particle size were explored to optimize ximenynic and juniperonic ethyl ester recovery and purity from ethyl ester mixtures using online UV/Vis detection. Particle size, followed by the stationary phase, were found to be the most important parameters to achieving good separation. Under optimized conditions, ximenynic and juniperonic ethyl ester purities greater than 99 and 95%, respectively, were achieved in a one step process without co-solvent. The isolation and recovery of juniperonic acid from biota seed oil free fatty acids was also attempted. Using free fatty acids as the feed material, the non-methylene interrupted polyunsaturated sciadonic acid was also able to be separated from other compounds including juniperonic acid under some conditions, and gave an increase in concentration of more than 17 times. 相似文献
16.
Biodiesel is gaining more and more importance as an attractive fuel due to the depleting fossil fuel resources. Chemically biodiesel is monoalkyl esters of long chain fatty acids derived from renewable feed stock like vegetable oils and animal fats. It is produced by transesterification in which, oil or fat is reacted with a monohydric alcohol in presence of a catalyst to give the corresponding monoalkyl esters. This article reports experimental data on the production of fatty acid methyl esters from vegetable oils, soybean and cottonseed oils using sodium hydroxide as alkaline catalyst. The variables affecting the yield and characteristics of the biodiesel produced from these vegetable oils were studied. The variables investigated were reaction time (1-3 h), catalyst concentration (0.5-1.5 w/wt%), and oil-to-methanol molar ratio (1:3-1:9). From the obtained results, the best yield percentage was obtained using a methanol/oil molar ratio of 6:1, sodium hydroxide as catalyst (1%) and 60 ± 1 °C temperature for 1 h. The yield of the fatty acid methyl ester (FAME) was determined according to HPLC. The composition of the FAME was determined according to gas chromatography. The biodiesel samples were physicochemically characterized. From the results it was clear that the produced biodiesel fuel was within the recommended standards of biodiesel fuel. 相似文献
17.
At present, the homogeneous base-catalyzed methanolysis reaction of vegetable oils is a most often used process for the industrial biodiesel production. The toxicity of methanol, the risk of the methanol vapor explosion and the possibility of the ethanol production from biorenewable resources have contributed to the development of a vegetable oil ethanolysis process for the biodiesel production. In the reaction of vegetable oils and ethanol in the presence of a catalyst, completely agricultural fuels consisted of fatty acid ethyl esters (FAEE) are obtained having physico-chemical properties similar to those of the appropriate methyl esters and diesel fuel. The ethanolysis reaction of various oily feedstocks has been widely studied to optimize the reaction conditions and to develop new catalytic systems and processes based on chemical and biological catalysts, as well as the development of non-catalytic processes. Most researches investigate the application of homogeneous base catalysts. This paper studies the review of vegetable oil ethanolysis investigations for the biodiesel production done so far. The goals of the paper are to present the development of FAEE synthesis by catalytic and non-catalytic processes, their advantages and disadvantages, the influence of some operating and reaction conditions on the process rate and ethyl esters yield, the kinetics models describing the ethanolysis process rate, the process optimization and the possibilities for improving the FAEE synthesis process. 相似文献
18.
A fractionally distilled C14−C16 fatty acid methyl ester, derived from palm oil, was sulfonated with gaseous SO3 in a falling film reactor to form an α-sulfo fatty acid methyl ester (α-SF; unbleached and unneutralized form). The included
dark-colored impurities were then separated from α-SF as a diethyl ether-insoluble matter. After purification by thin-layer
chromatography, the colored species were analyzed by ion-exchange chromatography, gel-permeation chromatography, and nuclear
magnetic resonance spectrometry. These data suggested that the colored species were polysulfonated compounds with conjugated
double bonds. Minor components in the raw fatty acid methyl ester, found by gas chromatography/mass spectrometry, were spiked
into the purified methyl palmitate and then sulfonated. The unsaturated methyl ester and hydroxy ester showed the worst color
results. The methyl oleate and methyl 12-hydroxystearate were then sulfonated and analyzed. Deep black products were obtained,
which showed the same properties as the colored species in α-SF. It was concluded that low levels of unsaturated fatty acid
methyl esters and hydroxy esters in the fatty acid methyl ester are the main causes of the coloring. 相似文献
19.
E. N. Frankel D. G. McConnell C. D. Evans 《Journal of the American Oil Chemists' Society》1962,39(6):297-301
A liquid-partition chromatographic procedure was used to separate hydroxy fatty acids, their methyl esters, and reduced fatty
ester hydroperoxides. Mixtures of methyl stearate, mono- and dihydroxystearate, and mixtures of the corresponding free fatty
acids were easily separated. Chromatographic determinations for ricinoleate in castor oils compared favorably with the chemical
and infrared analyses.
The chromatographic procedure was used to separate hydroxy fatty acids inDimorphotheca andStrophanthus seed oils. The methyl ester of dimorphecolic acid, the principal hydroxy fatty ester ofDimorphotheca oil, behaved like reduced methyl linoleate hydroperoxide and showed a polarity intermediate between methyl 12-hydroxystearate
and methyl 9,10-dihydroxystearate. The 9-hydroxy-12-octadecenoic ester ofStrophanthus oil had a larger retention volume than methyl ous hydroxy fatty esters isolated chromatographically. The diene content of
the reduced hydroperoxides agrees well with values reported in the literature (1,5,16). The diene content of the chromatographed
methyl dimorphecolate is higher than reported by Smithet al. (20) for their preparations but agrees well with the value reported by Chipault and Hawkins (6) for puretrans-trans conjugated methyl linoleate. The extinction coefficient of methyl 12-hydroxystearate at 2.8 μ is higher than that reported
for ricinoleate and the absorption band is much sharper. Because of these two conditions no association of the hydroxyl groups
is indicated. These results also confirm the purity of the hydroxy fatty esters obtained by LPC. This method has been a valuable
adjunct to the study of various oxygen-containing fatty acid and esters and was used to characterize the hydroxy esters obtained
from the hydrogenation of methyl linolenate hydroperoxides (9). This work offers a basis for the development of analytical
methods to determine the hydroxy and other polar acid content of fatty glycerides and their derivatives. 相似文献
20.
Kuan-hsiang Huang Casimir C. Akoh 《Journal of the American Oil Chemists' Society》1994,71(11):1277-1280
The ability of immobilized lipases IM60 fromMucor miehei and SP435 fromCandida antarctica to modify the fatty acid composition of selected vegetable oils by incorporation of n−3 polyunsaturated fatty acids into
the vegetable oils was studied. The transesterification was carried out in organic solvent with free acid and ethyl esters
of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) as acyl donors. With free EPA as acyl donor, IM60 gave higher
incorporation of EPA than SP435. However, when ethyl esters of EPA and DHA were the acyl donors, SP435 gave higher incorporation
of EPA and DHA than IM60. When IM60 and free acid were used, the addition of 5 μL water increased EPA incorporation into soybean
oil by 4.9%. With ethyl ester of EPA as acyl donor, addition of 2 μL water increased EPA incorporation by 3.9%. For SP435,
addition of water up to 2μL resulted in increased EPA incorporation, but the incorporation declined when the added water exceeded
this amount. The addition of water increased the EPA incorporation into Trisun 90 after 24 h reaction but not the reaction
rate at early stages of the reaction. 相似文献