Lipase catalyzed epoxidation of fatty acid methyl esters derived from unsaturated vegetable oils in absence of carboxylic acid
KeywordsEpoxidation FAME Lauric acid Lipase
fatty acid methyl esters
saturated fatty acid methyl ester
monounsaturated fatty acid methyl ester
polyunsaturated fatty acid methyl ester
In response to a serious concern over the depleting fossil reserves and the negative environmental impact caused by their products and processes, there has been a growing trend towards utilization of renewable feedstocks as a source of chemicals and materials . Vegetable oils and the product of their transformations (fatty acids and alkyl esters) are important raw materials for producing a variety of products such coatings, paints, lubricants, soaps , and inks . For more complex molecules such polymers, copolymers and their composites, the oils have to be chemically modified. One of the most interesting functional group for this purpose is the epoxy ring. Epoxides are major key raw materials for various industrial products such as polymer plasticizer, agrochemical, cosmetics, pharmaceuticals and food additives. Epoxidation consists on the formation of an oxirane (epoxy) group by the reaction of peroxyacids (peracids) and olefinic double bonds . Epoxides derived from vegetable oils are used as PVC stabilizers, plasticizers and in polyurethane production. They can also be useful as reactive diluents for paints, production of surfactants, corrosion protections agents and additives to lubricants. Using epoxidized FAMEs from unsaturated vegetable oils it is possible to obtain polymers and composites with better mechanical, electric, thermal properties than those of the polymers obtained from petrochemical products and greater resistance to oxidation than the latter ones [5, 6, 7].
During industrial epoxidation, the required peroxyacids are commonly produced by the reaction of acetic or formic acids and hydrogen peroxide in presence of strong mineral acids, such as H2SO4 and H3PO4 or by the direct addition of any peroxyacid which can cause equipment corrosion and promote undesirable oxirane ring-opening reactions [8, 9].
Recently, enzymatic epoxidation reactions have been better accepted compared with chemical synthesis due to the milder reactions conditions as formation of stable hydroperoxides directly from fatty acids, high stereoselectivity, significant suppression of side reactions and high conversion [10, 11, 12].
Materials and methods
Lipase B from Candida antarctica (Novozym 435) immobilized on macroporous polyacrylate resin beds, chloroform-d, cyclohexane, isooctane, dodecanoic acid (lauric acid) and pentadecanoic acid were acquire from Sigma-Aldrich. Potassium hydroxide, hydrogen peroxide 30% was purchased from J.T. Baker, toluene was acquired from Fermont, sodium hydroxide, potassium sulphate and anhydrous ethanol and methanol 99% were purchased Mallinckrodt. Vegetable oils (grapeseed, avocado and olive oils) were gotten from a local market (Additional file 1).
All experiments on this report were made at least by triplicate. Synthesis of epoxides involved two steps: in the first stride, different vegetable oils (grapeseed, avocado and olive) were converted into methyl esters by transesterification reaction using KOH as catalyst and methanol as acyl acceptor.
In a second step 1 g of methyl esters, 100 mg of Novozym 435, 1 mmol of lauric acid and 6 mL of toluene were added into a 50 mL round bottom flask, and then 5 mL of distillate water was added to the reaction mixture to create a biphasic system which was heated to 45 °C and homogenized with stirring. Once the temperature was reached and kept for 5 min, slowly 1 mL of hydrogen peroxide was added to the reaction system and the reactions were stirred at this temperature for 16 h. Upon completion of reaction time, samples were cooled to 4 °C and Novozym 435 was recovery by vacuum filtration, using filter paper number 41. The filtered reaction mixture was firstly washed several times with distilled water and the separated organic layer was dried with anhydrous sodium sulphate for 1 h to remove trace water and decompose traces of unreacted peroxides. Finally, product was separated from solvent using a vacuum rotary evaporator at 90 °C for 1 h. Experiments were repeated in absence of lauric acid under the same conditions of reactions.
Characterization of FAMEs and its epoxides
Fatty acid methyl esters (FAMEs) and its epoxidized products were analysed by gas chromatography (Agilent series 7890B) coupled with mass spectrometer (Agilent series 5975C) in a HP-INNOWAX column, 30 m × 0.25 mm, 0.25 μm and by nuclear magnetic resonance trough 1H-NMR and 13C-NMR experiments using a Bruker 400 MHz magnet and deuterated chloroform solvent for sample preparation.
Results and discussion
Conversion and percentage of saturated, mono and polyunsaturated FAMEs derived from vegetable oils
Effect of lauric acid in enzymatic epoxidation of FAMEs from vegetable oils
Initial experiments were performed in presence of carboxylic acid as lauric acid because has been reported that the use of linear chain fatty acids favours the reaction conversion into the corresponding epoxide due to the fatty acids acts as precursor in the epoxide formation [15, 16, 17]. Originally FAMEs from different vegetable oils did not contain epoxy groups but after epoxidation reactions their presence could be identified with chemical shifts due to double bonds (~ 5 ppm). Figures 1b, d and 2b shows the disappearance of this peaks which means epoxidation was completely carried out (conversion > 99%). A new signals at 2.90 ppm confirmed the existence of an epoxy ring corresponding to methine CH proton and at 1.50 ppm corresponding to the new methylene group alpha to the new epoxy group. Finally, signal at 1.63 ppm indicates a methylene group between the two new epoxy groups.
Experiments were also performed in absence of lauric acid in order to evaluate its effect in the epoxide formation. For these assays characteristics signals on the NMR spectra corresponding to epoxides were identified at 2.90, 1.50, and 1.63 ppm as in the previous experiments. Also, it was noticed the disappearance of peak belonging to double bonds (~ 5 ppm) where it can be inferred that conversion was more than 99% such as in the previous experiments. All 1H NMR signals from FAME and epoxides of FAME matched perfectly with previous reports .
Reaction mechanism involves two steps: Firstly, saturated and insaturated methyl esters present in the mixture of FAMEs from vegetable oils react with H2O2 to form the corresponding peracid, secondly peracid spontaneously donates the oxygen to a double bond of the unsaturated FAMEs (methyl oleate and methyl linoleate are used as example) to yield epoxystearic and diepoxystearic acid methyl ester respectively.
GC/MS analysis was used to evaluate the resulting epoxides structures on proposed mechanism. The epoxy stearate (9,10-epoxy octadecanoate) was identified at RT: 33.69 min and the mass spectrum allowed to define its molecular structure. The molecular ion (M+) was detectable at 312, the major fragments m/z 155 (M-157; loss of ·(CH2)7-COOCH3) and 199 (M-113; loss of ·(CH2)7-CH3) represent the result of cleavage at the epoxy ring .
The corresponding peak to diepoxy stearate (9,10-12,13-diepoxy octadecanoate) appeared at RT: 37.38 min and the molecular ion (M+) was perceptible at 326. The spectrum was similar at MS spectrum previous reported for the same compound [18, 20]. Characteristic peaks were identified at m/z 295 (M-31), 277 (M-49), 255 [CH2CH(O)CHCH2CH(O)CH(CH2)7COOCH3-14]+, 237 [CH2CH(O)CHCH2CH(O)CH(CH2)7COOCH3-32]+, and 211[O=CHCH2CH(O)CH(CH2)7COOCH3-31]+.
It is possible to obtain epoxides fatty acid methyl esters by an enzymatic reaction under mild temperature and pressure conditions (45 °C, 1 atm., 250 rpm) and high selectivity by the use of Novozym 435 as biocatalyst and hydrogen peroxide as oxygen donor. The reactions were carried out with conversions higher than 99%. This study also demonstrates that the addition of a carboxylic acid is not essential or crucial to perform epoxidation reactions successfully due to the fact that the unsaturated FAMEs present in the mixture generated by enzymatic hydrolysis act as precursors in the epoxide formation.
ASR carried out the experimental work. DCF is the corresponding author and wrote most of the manuscript. VRS contributed to data analysis and interpretation. JCEH and ACD carried out the spectroscopic characterization and GZG carried out the chromatographic analysis. All authors read and approved the final manuscript.
We gratefully acknowledge the financial support of the Facultad de Ciencias Químicas of the Universidad Autónoma de Chihuahua and the National Council of Science and Technology of Mexico (CONACyT).
The authors declare that they have no competing interests.
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- 7.Amoah J, Quayson E, Hama S, Yoshida A, Hasunuma T, Ogino C, Kondo A (2007) Simultaneous conversion of free fatty acids and triglycerides to biodiesel by immobilized Aspergillus oryzae expressing Fusarium heterosporum lipase. Biotechnol J 12:1–4Google Scholar
- 13.Naureen R, Tariq M, Yusoff I, Chowdhury A, Ashraf A (2015) Synthesis, spectroscopic and chromatographic studies sunflower oil biodiesel using optimized base catalysed methanolysis. J Biol Sci 22:332–339Google Scholar
- 14.Usman A, Thoss V, Darko G, Itodo AU (2016) Determination of triacylglycerol composition of Trichilia emetica seed oil using GC–MS and 1HNMR spectroscopy. Adv Anal Chem 6(1):10–16Google Scholar
- 19.Kaneshiro ES, Ellis J, Guo Z, Jayasimhulu K, Maiorano JN, Kallam KA (1996) Characterizations of neutral lipid fatty acids and cis-9,10-epoxy octadecanoic acid in Pneumocystis carinii carinii. Infect Immun 64:4105–4114Google Scholar
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