Synthesis of cross-linked comb-type polysiloxane for polymer electrolyte membranes
Hydrosilylation reaction of 2.4.6.8-tetrahydro-2.4.6.8-tetramethylcyclotetrasiloxane with allyl acetoacetate and vinyltriethoxysilane at 1:3:1 ratio of initial compounds in the presence of Karstedt’s catalyst (Pt2[(VinSiMe2)2O]3), platinum hydrochloric acid (0.1 M solution in THF) and platinum on th...
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sg-ntu-dr.10356-1021162023-07-14T15:50:12Z Synthesis of cross-linked comb-type polysiloxane for polymer electrolyte membranes Abadie, Marc J. M. Mukbaniani, Omar Aneli, Jimsher Tatrishvili, Tamara Markarashvili, Eliza Chigvinadze, Maia School of Materials Science & Engineering DRNTU::Engineering::Materials Hydrosilylation reaction of 2.4.6.8-tetrahydro-2.4.6.8-tetramethylcyclotetrasiloxane with allyl acetoacetate and vinyltriethoxysilane at 1:3:1 ratio of initial compounds in the presence of Karstedt’s catalyst (Pt2[(VinSiMe2)2O]3), platinum hydrochloric acid (0.1 M solution in THF) and platinum on the carbon have been studied and D4R,R’ type methylorganocyclotetrasiloxane has been obtained. Ring-opening co-polymerization reactions of methylorganocyclotetrasiloxane and hexamethyldisiloxane, in the presence of catalytic amount of powder-like potassium hydroxide, have been carried out and linear methylsiloxane oligomer with regular arrangement of propyl acetoacetate and triethoxysilane groups in the side chain has been obtained. The synthesized methylorganocyclotetrasiloxane and oligomers were studied by FTIR, 1H, 13C, 29Si NMR spectroscopy. Comb-type oligomers were characterized by gel-permeation chromatography, wide- angle X-ray and differential scanning calorimetric methods. Via sol-gel processes of doped with lithium trifluoromethylsulfonate (triflate) or lithium bis- (trifluoromethylsulfonyl)imide oligomer systems solid polymer electrolyte membranes have been obtained. The dependence of ionic conductivity as a function of temperature and salt concentration has been studied. The electrical conductivity of these materials at room temperature belongs to the range of 7x10-8 to 4x10-6 S cm-1 and depends on the structures of grafted anion receptors and the polymer backbones. Published version 2014-06-20T07:25:33Z 2019-12-06T20:49:58Z 2014-06-20T07:25:33Z 2019-12-06T20:49:58Z 2012 2012 Journal Article Mukbaniani, O., Aneli, J., Tatrishvili, T., Markarashvili, E., Chigvinadze, M., & Abadie, M. J. M. (2012). Synthesis of cross-linked comb-type polysiloxane for polymer electrolyte membranes. e-Polymers, 12(1), 1-14. 1618-7229 https://hdl.handle.net/10356/102116 http://hdl.handle.net/10220/19845 http://www.degruyter.com/view/j/epoly.2012.12.issue-1/epoly.2012.12.1.1023/epoly.2012.12.1.1023.xml en e-Polymers © 2012 De Gruyter. This paper was published in e-Polymers and is made available as an electronic reprint (preprint) with permission of De Gruyter. The paper can be found at the following official URL: http://www.degruyter.com/view/j/epoly.2012.12.issue-1/epoly.2012.12.1.1023/epoly.2012.12.1.1023.xml. One print or electronic copy may be made for personal use only. Systematic or multiple reproduction, distribution to multiple locations via electronic or other means, duplication of any material in this paper for a fee or for commercial purposes, or modification of the content of the paper is prohibited and is subject to penalties under law. application/pdf |
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DRNTU::Engineering::Materials Abadie, Marc J. M. Mukbaniani, Omar Aneli, Jimsher Tatrishvili, Tamara Markarashvili, Eliza Chigvinadze, Maia Synthesis of cross-linked comb-type polysiloxane for polymer electrolyte membranes |
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Hydrosilylation reaction of 2.4.6.8-tetrahydro-2.4.6.8-tetramethylcyclotetrasiloxane with allyl acetoacetate and vinyltriethoxysilane at 1:3:1 ratio of initial compounds in the presence of Karstedt’s catalyst (Pt2[(VinSiMe2)2O]3), platinum hydrochloric acid (0.1 M solution in THF) and platinum on the carbon have been studied and D4R,R’ type methylorganocyclotetrasiloxane has been obtained. Ring-opening co-polymerization reactions of methylorganocyclotetrasiloxane and hexamethyldisiloxane, in the presence of catalytic amount of powder-like potassium hydroxide, have been carried out and linear methylsiloxane oligomer with regular arrangement of propyl acetoacetate and triethoxysilane groups in the side chain has been obtained. The synthesized methylorganocyclotetrasiloxane and oligomers were studied by FTIR, 1H, 13C, 29Si NMR spectroscopy. Comb-type oligomers were characterized by gel-permeation chromatography, wide- angle X-ray and differential scanning calorimetric methods. Via sol-gel processes of doped with lithium trifluoromethylsulfonate (triflate) or lithium bis- (trifluoromethylsulfonyl)imide oligomer systems solid polymer electrolyte membranes have been obtained. The dependence of ionic conductivity as a function of temperature and salt concentration has been studied. The electrical conductivity of these materials at room temperature belongs to the range of 7x10-8 to 4x10-6 S cm-1 and depends on the structures of grafted anion receptors and the polymer backbones. |
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School of Materials Science & Engineering |
author_facet |
School of Materials Science & Engineering Abadie, Marc J. M. Mukbaniani, Omar Aneli, Jimsher Tatrishvili, Tamara Markarashvili, Eliza Chigvinadze, Maia |
format |
Article |
author |
Abadie, Marc J. M. Mukbaniani, Omar Aneli, Jimsher Tatrishvili, Tamara Markarashvili, Eliza Chigvinadze, Maia |
author_sort |
Abadie, Marc J. M. |
title |
Synthesis of cross-linked comb-type polysiloxane for polymer electrolyte membranes |
title_short |
Synthesis of cross-linked comb-type polysiloxane for polymer electrolyte membranes |
title_full |
Synthesis of cross-linked comb-type polysiloxane for polymer electrolyte membranes |
title_fullStr |
Synthesis of cross-linked comb-type polysiloxane for polymer electrolyte membranes |
title_full_unstemmed |
Synthesis of cross-linked comb-type polysiloxane for polymer electrolyte membranes |
title_sort |
synthesis of cross-linked comb-type polysiloxane for polymer electrolyte membranes |
publishDate |
2014 |
url |
https://hdl.handle.net/10356/102116 http://hdl.handle.net/10220/19845 http://www.degruyter.com/view/j/epoly.2012.12.issue-1/epoly.2012.12.1.1023/epoly.2012.12.1.1023.xml |
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1772827880025227264 |