Hayyan, M. and Aissaoui, T. and Hashim, M.A. and AlSaadi, M.A. and Hayyan, A. (2015) Triethylene glycol based deep eutectic solvents and their physical properties. Journal of the Taiwan Institute of Chemical Engineers, 50. pp. 24-30. ISSN 1876-1070, DOI https://doi.org/10.1016/j.jtice.2015.03.001.
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Abstract
Deep eutectic solvents (DESs) have been recently emerged as new ionic liquids (ILs) analogues. The low vapor pressure, inflammability, biodegradability and positive effect on the environment make DESs more favorable as neoteric solvents. In this study, triethylene glycol (TEG) was selected as a hydrogen bond donor (HBD) to form DESs with five types of phosphonium and ammonium salts, namely methyltriphenylphosphonium bromide (MTPB), benzyltriphenylphosphonium chloride (BTPC), allyltriphenylphosphonium bromide (ATPB), choline chloride (2-hydroxyethyl-trimethylammonium) (ChCl) and N,N-diethylenethanolammonium chloride (DAC). The physical properties of the synthesized DESs were measured such as freezing point, viscosity, electrical conductivity, Walden rule, density, pH and water content. In addition, the Fourier transform infrared spectroscopy (FTIR) was employed to study the functional groups. The experiments were conducted at different temperatures, i.e. 25-80 degrees C. It was found that DESs have suitable properties to be used in industrial processes such as separation, extraction, biochemical, petroleum and gas technology. (C) 2015 Taiwan Institute of Chemical Engineers. Published by Elsevier B.V. All rights reserved.
| Item Type: | Article |
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| Funders: | University of Malaya HIR-MOHE D000003-16001, University of Malaya Centre for Ionic Liquids (UMCiL) |
| Additional Information: | ISI Document Delivery No.: CL5HY Times Cited: 0 Cited Reference Count: 35 Cited References: Abbott AP, 2003, CHEM COMMUN, P70, DOI 10.1039/b210714g Abbott AP, 2007, CHEM-EUR J, V13, P6495, DOI 10.1002/chem.200601738 Carriazo D, 2012, CHEM SOC REV, V41, P4996, DOI 10.1039/c2cs15353j Chen BK, 2013, FLUID PHASE EQUILIBR, V350, P37, DOI 10.1016/j.fluid.2013.04.009 D'Agostino C, 2011, PHYS CHEM CHEM PHYS, V13, P21383, DOI 10.1039/c1cp22554e Gore S, 2011, GREEN CHEM, V13, P1009, DOI 10.1039/c1gc00009h Hayyan A, 2012, THERMOCHIM ACTA, V541, P70, DOI 10.1016/j.tca.2012.04.030 Hayyan A, 2013, J MOL LIQ, V178, P137, DOI 10.1016/j.molliq.2012.11.025 Hayyan A, 2013, IND CROP PROD, V46, P392, DOI 10.1016/j.indcrop.2013.01.033 Hayyan A, 2013, CHEM ENG SCI, V92, P81, DOI 10.1016/j.ces.2012.12.024 Hayyan M, 2010, FUEL PROCESS TECHNOL, V91, P116, DOI 10.1016/j.fuproc.2009.09.002 Hayyan M, 2013, CHEMOSPHERE, V90, P2193, DOI 10.1016/j.chemosphere.2012.11.004 Jessica LA, 2008, IONIC LIQUIDS SYNTHE, P81 Jhong HR, 2009, ELECTROCHEM COMMUN, V11, P209, DOI 10.1016/j.elecom.2008.11.001 Kareem MA, 2012, FLUID PHASE EQUILIBR, V333, P47, DOI 10.1016/j.fluid.2012.07.020 Krolikowska M, 2012, THERMOCHIM ACTA, V530, P1, DOI 10.1016/j.tca.2011.11.009 Leron RB, 2013, THERMOCHIM ACTA, V551, P14, DOI 10.1016/j.tca.2012.09.041 Leron RB, 2012, J TAIWAN INST CHEM E, V43, P551, DOI 10.1016/j.jtice.2012.01.007 Leroy E, 2012, GREEN CHEM, V14, P3063, DOI 10.1039/c2gc36107h Lindberg D, 2010, J BIOTECHNOL, V147, P169, DOI 10.1016/j.jbiotec.2010.04.011 Luo JS, 2012, J MATER CHEM, V22, P20574, DOI 10.1039/c2jm34359b Nuntaphan A, 2002, APPL THERM ENG, V22, P251, DOI 10.1016/S1359-4311(01)00088-6 Pinkert A, 2011, PHYS CHEM CHEM PHYS, V13, P5136, DOI 10.1039/c0cp02222e Rimsza JM, 2012, COMPUT THEOR CHEM, V987, P57, DOI 10.1016/j.comptc.2011.11.003 Roeges NPG, 1994, GUIDE COMPLETE INTER Schreiner C., 2009, J CHEM ENG DATA, V55, P1784, DOI DOI 10.1021/JE900878J Shahbaz K, 2012, THERMOCHIM ACTA, V527, P59, DOI 10.1016/j.tca.2011.10.010 Shahbaz K, 2011, ENERG FUEL, V25, P2671, DOI 10.1021/ef2004943 Shahbaz K, 2011, SEP PURIF TECHNOL, V81, P216, DOI 10.1016/j.seppur.2011.07.032 Siongco KR, 2013, THERMOCHIM ACTA, V566, P50, DOI 10.1016/j.tca.2013.05.023 Smith B. C., 1999, INFRARED SPECTRAL IN Stuar BH, 2004, INFRARED SPECTROSCOP Wojnarowska Z, 2013, PHYS REV LETT, V111, P225 Xiuli Wang X, 2009, ADV NATURAL GAS ENG Zhang QH, 2012, CHEM SOC REV, V41, P7108, DOI 10.1039/c2cs35178a Hayyan, Maan Aissaoui, Tayeb Hashim, Mohd Ali AlSaadi, Mohammed AbdulHakim Hayyan, Adeeb Engineering, Faculty /I-7935-2015 Engineering, Faculty /0000-0002-4848-7052 University of Malaya HIR-MOHE D000003-16001; University of Malaya Centre for Ionic Liquids (UMCiL) The authors would like to express their thanks to University of Malaya HIR-MOHE (D000003-16001) and University of Malaya Centre for Ionic Liquids (UMCiL) for their support to this research. We would also like to thank Hanee Farzana Hizaddin for her assistance in using Turbomole and COSMOthermX. 0 ELSEVIER SCIENCE BV AMSTERDAM J TAIWAN INST CHEM E |
| Uncontrolled Keywords: | Deep eutectic solvent, Ionic liquid, Triethylene glycol, Choline, chloride, Phosphonium salt, Hydrogen bond donor, OIL-BASED BIODIESEL, PALM-OIL, ETHYLENE-GLYCOL, IONIC LIQUIDS, AMMONIUM, TEMPERATURE, DENSITIES, MIXTURES, GLYCEROL, CATALYST, |
| Subjects: | T Technology > T Technology (General) T Technology > TA Engineering (General). Civil engineering (General) T Technology > TP Chemical technology |
| Divisions: | Faculty of Engineering |
| Depositing User: | Mr Jenal S |
| Date Deposited: | 09 Mar 2016 02:46 |
| Last Modified: | 19 Mar 2019 03:37 |
| URI: | http://eprints.um.edu.my/id/eprint/15681 |
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