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...
Saved in:
Main Authors: | , , , , |
---|---|
Other Authors: | |
Format: | Article |
Language: | English |
Published: |
2022
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/161987 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
id |
sg-ntu-dr.10356-161987 |
---|---|
record_format |
dspace |
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 |
_version_ |
1749179147637227520 |