KiMYA PROBLEMLORi № 4 2017 ISSN 2221-8688
387
UDC 544.653/.653.3. 541.139
RESEARCH INTO THE PRODUCTION PROCESS OF BIODIESEL ETHERS BY USING AMINE-CONTAINING CATALYST IN MAGNETIC FIELD
M.M. Abbasov
Yu.G. Mamedaliyev Institute of Petrochemical Processes of the National Academy of Sciences ofAzerbaijan,
Laboratory of Renewable fuels Khojalipr., 30, Baku AZ1025, Azerbaijan Republic; e-mail: mutallim.abbasov@rambler.ru
The production of biodiesel esters by transesterification of corn and sunflower oil with methanol has been analyzed using 1,3-bis (isopropylamino)-propan-2-ol catalyst in 15-45mT magnetic field, at 65°C temperature and 6:1 molar ratio of methanol to oil. Experiments were carried out in three-neck round-bottom flask which is placed in magnetic field produced by electromagnets and equipped with a thermometer, a mixer and a dropping funnel. The yield of the biodiesel ester was 95-97% (by mass) and the duration of the process was 4.5 times shorter with magnetic field when the catalyst is used at 3% by weight relative to oil.
Keywords: biodiesel, transesterification, amine-containing catalysts, magnetic field
INTRODUCTION
Nowadays, approved petroleum reserves of the world are 157 billion tons and according to estimates, it will meet energy requirement for 40-50 years. In consdering the fact that the poisonous waste are those produced due to the combustion of petroleum-based energy carriers which deteriorate the ecology, the world energetics should use renewable and more environmentally-convenient fuels [1].
In order to accomplish the process, a number of leading countries are accepting various programs and a budget of high amount of money [2,].
For instance, 1.5 billion dollars of public investment will be spent during the upcoming decade for the development of bioeconomics in the United States of America. The purpose of this investment is 25/25, i.e. to use 25% of alternative renewable energy of total energy resources until 2025. According to estimates, it may save 35% of petroleum consumption (10 million barrel per day) until 2030; reduce 80% of greenhouse gases and thus lead climate changes in the world until 2050.
The similar program has been accepted in the European Union (EU). Executive Center of the EU predicts the usage of the alternative energy sources reaching to 20% and the amount of the contamination to the atmosphere being reduced by 20% by 2020 with respect to the pointers of 1990. Since 2013, the plan that is called "20-20-20" has been providing the transfer of quota sale of the EU members for CO2 contaminants [2].
The manufacture of energy carriers from the biological feedstock is the easiest and the most cost effective process, and widely used among other renewable energy sources. Considering that the major part of the fuel energy is consumed by automobiles, the application of alternative biofuels in the transportation industry becomes very essential [3-5].
The main advantages of the biofuels are their production from renewable feedstock, being sulfur free and rich in aromatics, biodegradibility (most feedstock degrade in about 2 months) and environmentally friendly gaseous waste. As a result of ethanol usage, the
greenhouse gases (CO2 equivalent) decreased by 8 million tonnes, which equalled to the total annual emissions of 1.21 million cars in the USA in 2008 [1]. Greenhouse gases emitted from renewable biosources do not contribute to the global CO2 growth in the atrmosphere since the amount of the CO2 released into the atmosphere corresponds to the amount absorbed by the plants. EU's "Encourage for the usage of biofuels" directive specifies following components as biofuel: bioethanol, biodiesel, biogas, biomethanol, the ether of biodimethyl, bio-ETBE (ethyl-tert-butyl ether) produced from bioethanol, bio-MTBE (methyl- tert-butyl ether) produced from biomethanol, synthetic biofuel, biohydrogen and vegetable oils.
Nowadays, biofuels are already being used as an alternative fuel for diesel engines. Biodiesel consists of alkyl esters of fatty acids produced by transesterification of various vegetable oils with alcohols. These kinds of molecules provide oxygen into combustion products in the oxygen-deficient environment as they contain the oxygen atoms. By this way, the oxygen atoms in biodiesel are used during the combustion process to cause complete burning. For instance, switching to B100 (100% biodiesel) from conventional diesel, causes 56.3% decrease of incompletely burned hydrocarbons, 55.4% decrease of solid particles and 43.2% decrease of carbon dioxide. Considering that the incompletely burned
gaseous waste from automobile emissions get into the human respiratory system for a long time and risk potentially causing the lung cancer, especially in big cities where the emissions are high, the combustion products have to be purified.
Currently, the most widespread method for preparing biodiesel is the transesterification of vegetable oils (or fatty acids obtained from them) with alcohols in the presence of alkaline catalyst in mixing batch reactor. Despite being simple in technology, this process has some disadvantages. The most important one is that the feedstock need to be dried, otherwise it will cause saponification, lowering the yield of the desired products. Produced soap hinders the separation process of ester/glycerol phases as a surfactant and raises the production cost by up to 30% [6-8].
The production of biodiesel esters is optimized in a number of ways, including testing new catalysts capable of preventing saponification, increasing rates of the transesterification process by using electromagnetic and magnetic waves, etc. Note that the use of magnetic field weakens chemical bonds in the molecules as a result of polarization/depolarization processes which accordingly raise the reaction rate [9,10].
Results of various studies utilizing amine-containing catalyst for the transesterification of fatty acids is given in Table 1 [11-15].
Catalyst Amount,% by mass, according to oil Reaction time, hour pKa The yield of alkyl ethers, % by mass
1,5,7-triazabicyclo[4,4,0]dec-5-ene (TBD) [5,6] 1 1 25,9 89
1,5,7-triazabicyclo[4,4,0] dec-5-ene (TBD) 2 1 — 91
1,5,7-triazabicyclo [4,4,0] dec-5-ene (TBD) 3 1 — 93
Tris-(dimethylamino)methyliminophosphorane (Me7P) [7] 1 1 27.5 63
1,8 -diazabicyclo[5,4,0]undec-7-ene (DBU) 1 1 24.32 32
Table 1. Relative activity of miscellaneous amine-containing compounds as transesterification
catalyst.
[5,7,8,9]
1,1,3,3-tetramethylguanidine (TMQ) [10-12] 1 1 23.30 18
1,5 diazabicyclo[4,3,0] non-5-ene (DBN) [7,9] 1 1 23.79 45
As is seen from the Table 1, TBD and Me7P catalysts show highest activities among other tested amines for transesterification process. For example, when 1,5,7-triazabicyclo[4,4,0] dec-5-ene is used (oil:alcohol ratio 1:4, temperature 70°C) the 1%
and 3% of catalyst yielded 91% and 93% of biodiesel esters, respectively. In order to obtain 98-99% yield by using conventional KOH and NaOH catalysts, amine containing catalysts should be used above 3% by mass.
EXPERIMENTALS
In this proceeding, we examined the production process of the biodiesel esters from corn and sunflower oils and methanol using 1,3-bis (isopropylamino)-propan-2-ol catalyst in 15-45mT magnetic field and at 65°C temperature. Methanol to oil ratio was set at 6:1. The experiments were carried out in three-neck
round-bottom flask equipped with a thermometer, a mixer, and a dropping funnel and placed in the magnetic field produced by electromagnets. Amount of catalyst (relative to oil) varied in the interval of 1-3%. Refined corn and sunflower oils and unrefined sunflower oil were used as vegetable oils.
RESULTS AND DISCUSSION
Yields of biodiesel ethers produced by using 1,3-bis (isopropylamino)-propan-2-ol as catalyst are given in Table 2.
Table 2. The dependence of the yields of biodiesel ethers on the duration of process by using 1,3-bis (isopropylamino)-propan-2-ol as catalyst with and without* magnetic field
Duration of process Refined sunflower Unrefined sunflower Refined Corn
Yields of biodiesel ethers with 1% catalyst
40 minutes 40/22* 45/26 41/ 24
2 hours 62/ 45 68 / 48 60 / 43
4 hours 72 / 58 81/ 62 75 / 60
Yields of biodiesel ethers with 3% catalyst
40 minutes 95 / 61 97 / 65 96 / 62
2 hours 96 / 71 98 / 75 98 / 75
4 hours 98 / 89 98 / 91 98 / 90
Note that the yield of biodiesel esters varied at 22-26% (by weight) interval after 40 minutes in normal conditions when the 1% catalyst was used by weight. However, when the magnetic field was applied, the yields were doubled within the same duration to make up 43-46%. Also, yields of biodiesel esters were 43-48% and 58-62% during 2 and 4 hours of the
conventional process, respectively, whereas they increased to 62-68% and 72-81%, respectively, with magnetic field. The yield has reached to 95-97% by weight in 40 minutes and under magnetic field when the amount of the catalyst rose to 3%. However, under standard conditions, an appropriate yield was 61-65% and even after 4 hours, it only reached to 90-91%. The purity
of synthesized methyl esters of sunflower and NMR spectroscopy methods (Figure 1). corn oils have been verified by using 1H and 13C
Ma._____ . M .
JUL
_flU_1
2 9 28
JllliL
1 13
Fig.1 H, C NMR spectra of the methyl ether of sunflower oil
Note that protons of methyl and methylene groups, as well as those belonging to unsaturated hydrocarbon radicals have been observed in 1.35 (3H, CH3) and 1.35-1.5 (20H, 10 CH2) ppm, however, the allyl protons of allyl group and the protons of metoxy group have been recorded in 2.1-2.2 (4H, 2CH2C=C) and 3.75 (3H, OCH3) ppm.
Signals according to the following chemical shift have been recorded via NMR 13C spectrum: 22.8 (CH3), 24.8 (CH2), 27.4 (CH2), 29.2 (CH2), 29.5(CH2),29.7(CH2), 29.9(CH2), 31.6(CH2), 32.1(CH2), 33.8(CH2), 61.6(CH2), 68.8 (OCH3),128.05,128.2, 129.8, 130 (CH2=C and C=C).
RESULTS
Following the experiments in question, it catalyst for the transesterification process of was revealed that synthesized 1,3-bis both refined and unrefined vegetable oils with (isopropylamino)-propan-2-ol might be used as methanol if it is taken with 3% (by mass)
according to oil. Advantages of this catalyst are that it is soluble in methanol as a solid substance to create a precipitation during the usage of alcohol in reaction and may be reused, for it is easily separated from the reaction products. When the process runs under the influence of 15-45mT magnetic field, the duration of the reaction decreases 4.5 times.
It should be mentioned that at the beginning of the transesterification process, 3-bis (isopropylamino)-propan-2-ol, which is used as catalyst is dissolved in methanol and led to the reaction environment, whereas at the end, when the methanol is used and the excess amount is dismissed, it precipitates as a crystal and may be reused as catalyst by removing from products very easily.
REFERENCES
1. Rustamov M.I., Abbasov V.M., Mamedova T.A., Piriyev N.N. The environmental problems of the Earth and alternative energy sources. Baku: Elm Publ., 2008, 717 p. (In Azerbaijan).
2. Van Gerpen J.H., He B.B. Biodiesel and renewable diesel production methods. Advances in Biorefineries, 2014, pp. 441475.
3. Mammadova T.A., Babayeva F.A., Rustamov M.I. Biodiesel fuel- modern state and prospects. Processes of petrochemistre and oil refining. 2006, no. 4(27), pp. 15. (In Azerbaijan).
4. Raheman H. and Phadatare A. G. Diesel Engine Emissions and Performance from Blends of Karanja Methyl Ester and Diesel. Biomass and Bioenergy. 2004, vol. 27, pp. 393-397.
5. Ramadhas A.S., Jayaraj S., Muraleedharan C. Use of Vegetable Oils as I.C Engine Fuels: A Review. Renewable Energy. 2004, vol. 29, pp. 727-742.
6. Ramadhas A.S., Jayaraj S., Muraleedharan C. Biodiesel Production from high FFA rubber seed oil. Fuel. 2005, vol. 84, pp. 335-340.
7. Mammadova T.A., Talibov A.H., Andrushenko N.K., Askerova E.N., Veliev X.R., Alieva Z.M. Amine containing compounds as catalyst for producing of biodiesel fuels. / International conference «Catalysis for renewable sources: fuel, energy, chemicals». St.-Peterburg, Tsars Village, 2010, p. 123. (In Rusian).
8. Ramalho H. , Ferreira K. & oth. Production of Additives with Antimicrobial Activity via Tandem Hydroformylation-amine Condensation of Soybean FAME Using an Ionic Liquid-Based Biphasic Catalytic System. J. Braz. Chem. Soc., 2016, vol. 27 (2 ), pp. 236-244.
9. Colucci J.A., Borrero E.E., Alape F.J. Biodiesel from an alkaline transesterification reaction of soybean oil usinq ultrasonic mixing. Journal of American Oil Chemists Society. 2005, vol. 82, Isue 7, pp.525-530.
10. Manco I., Giordani L., Vaccari V., Oddone M. Microwave technology for the biodiesel production: Analytical assessments. Fuel . 2012, vol. 95, pp. 108112.
11. Liu S.Z., Wang F., . Stiles A.R. & oth. Ionic liquids for biofuel production: Opportunities and challenges. Applied Energy. 2012, vol. 92, P. 406-414.
12. Fang Z., Smith J.R., Qi X. Production of Biofuels and Chemicals with Ionic Liquids. Biofuels and Biorefineries. Springer, 2014, ISSN: 2214-1537.
13. Andrean L.I., Rocha J.D. Use of ionic liquids in biodiesel production: a review. Brazilian Journal of Chemical Engineering. 2012, vol. 29, no. 01, pp. 1-13.
14. Liang X., Yang J. Synthesis of a novel multi-SO3H functionalized ionic liquid and its catalytic activities for biodiesel synthesis. Green Chemistry. 2010, vol. 12, pp. 201-204.
KiMYA PROBLEML9RÎ № 4 2017
15. Earle M.J., Plechkova N.V., Seddon K.R. liquids. Pure Appl. Chem. 2009, vol. 81, Green synthesis of biodiesel using ionic no. 11, pp. 2045-2057.
ИССЛЕДОВАНИЕ ПРОЦЕССА ПОЛУЧЕНИЯ БИОДИЗЕЛЬНЫХ ЭФИРОВ С ИСПОЛЬЗОВАНИЕМАМИНСОДЕРЖАЩЕГО КАТАЛИЗАТОРА В МАГНИТНОМ
ПОЛЕ
М.М. Аббасов
Институт нефтехимических процессов им акад. Ю. Мамедалиева Национальной АН Азербайджана AZ1025 Баку, пр.Ходжалы, 30; e-mail: mutallim.abbasov@rambler.ru
Исследован процесс синтеза биодизельных эфиров путем переэтерификации кукурузного и подсолнечного масла метанолом с использованием в качестве катализатора 1,3-бис(изопропиламино)-пропан-2-ола в магнитном поле интенсивностью 15-45 мТ, температуре 65 ° С и молярном соотношении метанол:масло 6:1. Эксперименты проводились в оборудованной термометром, смесителем и капельной воронкой трехгорлой круглодонной колбе, помещаемой в магнитное поле, создаваемое электромагнитами. Выход биодизельного эфира составил 95-97% масс. при использовании катализатора в количестве 3% масс. При этом продолжительность реакции уменьшилась в 4.5 раза по сравнению с процессом, проводимом без использования магнитного поля.
Ключевые слова: биодизель, переэтерификация, аминсодержащие катализаторы, магнитное поле
bíodízel efírlorínínamíntorkíblíkatalízator vo maqnítsahosí
TOSÍRÍNDO ALINMASIPROSESÍNÍN TODQÍQÍ M.M. Abbasov
AMEA Y. Mdmmdddliyev adina Neft-Kimya Prosesbri institutu Az 1025 Baki, Xocali prospekti, 30; e-mail: mutallim.abbasov@rambler.ru
Biodizel efirldrinin sintez prosesi qargidali vd gündbaxan yaglarinin metanolla transefirld^mdsild 1,3-bis (isopropilamino)-propan-2-oldan katalizator kimim içtifadd etmdkld 15-45mT maqnit sahdsindd, 65°C temperaturda vd spirt:yag nisbdti 6:1 olduqda tddqiq edilmiçdir. Tdcrübdldr termometr, qariçtirici vd damcilayici qifla tdchiz olunmuç vd elektromaqnitldr vasitdsild yaradilmiç maqnit sahdsindd yerld$dirililmi$ ûç boqazli kolbada aparilmiçdir. Katalizatorun miqdari yaga gôrd 3% olduqda biodizel efirildrinin çiximi 95-97% (kütld) td^kil etmiç vd bu zaman prosesin aparilma müdddti maqnit sahdsinin tdsiri olmadan aparilan proses ild müqayisddd 4.5 azalmiçdir.
Açar sôzfor: biodizel, transefirld^md, amin tdrkibli katalizator, maqnit sahdsi
Received 29.10.2017.