Fluoroalkylated-GAP co-polymers (GAP-FP) as promising energetic binders

The development of a novel energetic block co-polymer of Glycidyl Azide Polymer (GAP) and the fluoropolymer (FP) using the Boron trifluoride-tetrahydrofuranate complex/diol initiator system is reported herein. Well-defined compositions of the GAP-FP co-polymers in two different GAP to FP ratios (1:1...

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Main Authors: See, Anders Yang Feng, Pisharath, Sreekumar, Ong, Yew Jin, Tay, Chor Yong, Hng, Huey Hoon
Other Authors: School of Materials Science and Engineering
Format: Article
Language:English
Published: 2022
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Online Access:https://hdl.handle.net/10356/161987
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1619872022-10-08T23:31:02Z Fluoroalkylated-GAP co-polymers (GAP-FP) as promising energetic binders See, Anders Yang Feng Pisharath, Sreekumar Ong, Yew Jin Tay, Chor Yong Hng, Huey Hoon School of Materials Science and Engineering Emerging nanoscience Research Institute Engineering::Materials::Functional materials Energetic Binder Fluoropolymer The development of a novel energetic block co-polymer of Glycidyl Azide Polymer (GAP) and the fluoropolymer (FP) using the Boron trifluoride-tetrahydrofuranate complex/diol initiator system is reported herein. Well-defined compositions of the GAP-FP co-polymers in two different GAP to FP ratios (1:1 & 1:3) were synthesized by tailoring the desired molecular weights of each block in the co-polymer, demonstrating the synthetic versatility of such a co-polymer system. The resultant GAP-FP co-polymers represent a unique hybrid binder system with tunable energy releasing and oxidizing potentials intended for metallized formulations. Thermogravimetric analysis showed that the carbonaceous residue usually formed from the decomposition of GAP could be reduced significantly by the copolymerization with FP. Isoconversional method of kinetic analysis of the GAP-FP copolymers revealed an increasing dependence of the effective activation energy on the extent of conversion. The increasing dependence suggested a mechanism of the competing reactions that were found to be between the reactions of fluoropolymer triggered oxidation and intermolecular crosslinking of the polyimine intermediates formed from GAP decomposition that ultimately resulted in the reduction of the carbonaceous residue. Submitted/Accepted version 2022-10-03T03:01:50Z 2022-10-03T03:01:50Z 2022 Journal Article See, A. Y. F., Pisharath, S., Ong, Y. J., Tay, C. Y. & Hng, H. H. (2022). Fluoroalkylated-GAP co-polymers (GAP-FP) as promising energetic binders. Reactive and Functional Polymers. https://dx.doi.org/10.1016/j.reactfunctpolym.2022.105415 1381-5148 https://hdl.handle.net/10356/161987 10.1016/j.reactfunctpolym.2022.105415 en Reactive and Functional Polymers © 2022 Published by Elsevier B.V. All rights reserved. This paper was published in Reactive and Functional Polymers and is made available with permission of Elsevier B.V. application/pdf application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Engineering::Materials::Functional materials
Energetic Binder
Fluoropolymer
spellingShingle Engineering::Materials::Functional materials
Energetic Binder
Fluoropolymer
See, Anders Yang Feng
Pisharath, Sreekumar
Ong, Yew Jin
Tay, Chor Yong
Hng, Huey Hoon
Fluoroalkylated-GAP co-polymers (GAP-FP) as promising energetic binders
description The development of a novel energetic block co-polymer of Glycidyl Azide Polymer (GAP) and the fluoropolymer (FP) using the Boron trifluoride-tetrahydrofuranate complex/diol initiator system is reported herein. Well-defined compositions of the GAP-FP co-polymers in two different GAP to FP ratios (1:1 & 1:3) were synthesized by tailoring the desired molecular weights of each block in the co-polymer, demonstrating the synthetic versatility of such a co-polymer system. The resultant GAP-FP co-polymers represent a unique hybrid binder system with tunable energy releasing and oxidizing potentials intended for metallized formulations. Thermogravimetric analysis showed that the carbonaceous residue usually formed from the decomposition of GAP could be reduced significantly by the copolymerization with FP. Isoconversional method of kinetic analysis of the GAP-FP copolymers revealed an increasing dependence of the effective activation energy on the extent of conversion. The increasing dependence suggested a mechanism of the competing reactions that were found to be between the reactions of fluoropolymer triggered oxidation and intermolecular crosslinking of the polyimine intermediates formed from GAP decomposition that ultimately resulted in the reduction of the carbonaceous residue.
author2 School of Materials Science and Engineering
author_facet School of Materials Science and Engineering
See, Anders Yang Feng
Pisharath, Sreekumar
Ong, Yew Jin
Tay, Chor Yong
Hng, Huey Hoon
format Article
author See, Anders Yang Feng
Pisharath, Sreekumar
Ong, Yew Jin
Tay, Chor Yong
Hng, Huey Hoon
author_sort See, Anders Yang Feng
title Fluoroalkylated-GAP co-polymers (GAP-FP) as promising energetic binders
title_short Fluoroalkylated-GAP co-polymers (GAP-FP) as promising energetic binders
title_full Fluoroalkylated-GAP co-polymers (GAP-FP) as promising energetic binders
title_fullStr Fluoroalkylated-GAP co-polymers (GAP-FP) as promising energetic binders
title_full_unstemmed Fluoroalkylated-GAP co-polymers (GAP-FP) as promising energetic binders
title_sort fluoroalkylated-gap co-polymers (gap-fp) as promising energetic binders
publishDate 2022
url https://hdl.handle.net/10356/161987
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