Investigation on synthesis of two ammonium based ionic liquids from fatty acids and triethylamine
DOI:
https://doi.org/10.51316/jca.2023.012Keywords:
Ionic liquid, synthesis, fatty acid, triethyl amineAbstract
Two ionic liquids triethylammonium oleate and triethylammonium stearate were synthesized from fatty acids and triethyl amine using two different methods (one step and three step methods). The yield triethylammonium oleate rearch 68.8-74% (one step method) and 86.3% (three step method) and of triethylammonium stearate rearch 68.7-74.1 (one step method) and 83.5% (three step method). The one step method spends more time but less chemicals and brings higher yield. FT-IR and 1H-NMR spectra of ILs obtained from both method was measured. The results showed that synthesis method doesn’t affect on the structure of the products and ILs obtained from one step method has higher purity.
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María-Dolores Bermúdez, Ana-Eva Jiménez, José Sanes and Francisco-José Carrión, Molecules 14 (2009) 2888-2908. https://10.3390/molecules14082888
Dupont, J. On the solid, J.Braz. Chem. Soc. 15 (2007) 341-350. https://10.1590/s0103-50532004000300002
Brenecke, J.F., Rogers, R.D., Seddon, K.R., Eds.; ACS Symposium Series 975 (2007) 86-101.
https://10.1021/bk-2007-0975.ch007
Consorti, C.S.; Suarez, P.A.Z.; de Souza, R.A.; Farrar, D.H.; Lough, A.J.; Loh, W.; da Silva,
L.H.M.; Dupont, J. Phys. Chem. B 109 (2005) 4341-4349. https://doi.org/10.1021/jp0452709
Ye, C.F.; Liu, W.M.; Chen, Y.X.; Yu, L.G. Chem. Commun. (2001) 2244-2245. https://10.1039/B106935G
Minami, I.; Kamimuram, H.; Mori, J. Synth. Lubr. 24 (2007) 135-147.
https://doi.org/10.1002/jsl.36
Yue Yang, Fanhan Liu, Shaole Song, Honghu Tang, Shitian Ding, Wei Suna, Shuya Lei, Shengming Xu, Lubricants 1 (2013) 3-21, https://doi.org/10.3390/lubricants1010003
Nicole Do¨rr, Proc IMechE Part J: J Engineering Tribology 226 (11) 889–890. https://10.1177/1350650112464332
Jeewan Singh, Sukhpal Singh Chatha, Rakesh Bhatia, Materials Today: Proceedings 56 (2022) 2659–2665. https://10.1016/j.matpr.2021.09.228
Zhaozhao Yang, Bian Guo, Yijing Liang, Qing Huang, Feizhou Li, Ruozheng Wang, Xiaoyan Yan, Bo Yu, Qiangliang Yu, Meirong Cai, Journal of Molecular Liquids 363 (2022) 119837. https://doi.org/10.1016/j.molliq.2022.119837
P. Oulego, D. Blanco, D. Ramos, J.L. Viesca b,c, M. Díaz, A. Hernández Battez, Journal of Molecular Liquids 272 (2018) 937–947, https://doi.org/10.1016/j.molliq.2018.10.106
Tulia Espinosa, José Sanes, Ana-Eva Jiménez, María-Dolores Bermúdez, Wear 303 (2013) 495–509. https://doi.org/10.1016/j.wear.2013.03.041
Ghassan M.J. Al Kaisy, M. Ibrahim A. Mutalib, T V V L N Rao, Adolfo Senatore, Tribology International 160 (2021) 107058.
M.D. Avil´es , R. Pamies , J. Sanes , J. Arias-Pardilla , F.J. Carrion, M.D. Bermúdez, Tribology International 158 (2021) 106917 https://doi.org/10.1016/j.triboint.2021.107058
Raimondas Kreivaitis, Arturas Kupcinskas, Audrius Zunda, Thi Na Ta, Jeng Haur Horng, Wear (2022) 492-493 204217. https://doi.org/10.1016/j.wear.2021.204217
J. L. Viesca, M.T. Mallada b, D. Blanco, A. Fernandez-Gonz alez, J. Espina-Casado c, R. Gonz alez, Tribology International 116 (2017) 422–430. https://doi.org/10.1016/j.triboint.2017.08.004
Bui, T. T. L. A. D. Nguyen, S. Ho-Van and H. T. N. Uong. Journal of Applied Polymer Science 133 (2016) 43920. https://doi.org/10.1002/app.43920
Bui, T. T. L. H. T. N. Uong, L. V. Nguyen and N. C. Pham. Chemical and Biochemical Engineering Quarterly 32 (2018) 41. https:10.15255/CABEQ.2017.1193
Bui, T. T. L, H. T. N. Uong, D. K. Nguyen, D. T. K. Hoang and G. Vo-Thanh. Korean Journal Chemical Engineering 37 (2020) 2262. https://doi.org/10.1007/s11814-020-0659-2
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