Synthesis and characterization glycidyl azide polymer of an attractive binder for energetic materials

The glycidyl azide polymer (GAP), known as an energetic, thermally stable, low sensitive, hydroxyl-terminated prepolymer, was synthesized using different diol and triol initiator units. GAP was prepared by azidation of poly(epichlorohydrin) (PECH) with different polyol units in the polymer chain. PE...

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Main Authors: Nešić Jovica, Marinković Aleksandar, Bajić Zoran, Brzić Saša
Format: Article
Language:English
Published: Military Technical Institute, Belgrade 2018-01-01
Series:Scientific Technical Review
Subjects:
Online Access:https://scindeks-clanci.ceon.rs/data/pdf/1820-0206/2018/1820-02061802026N.pdf
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spelling doaj-9a80f44ac3b3432abe5daa30f7ee226e2020-11-25T03:21:43ZengMilitary Technical Institute, BelgradeScientific Technical Review1820-02062683-57702018-01-0168226351820-02061802026NSynthesis and characterization glycidyl azide polymer of an attractive binder for energetic materialsNešić Jovica0Marinković Aleksandar1Bajić Zoran2https://orcid.org/0000-0002-8492-3333Brzić Saša3Military Technical Institute (VTI), BelgradeUniversity of Belgrade, Faculty of Technology and MetallurgyUniversity of Defence, Military Academy, BelgradeMilitary Technical Institute (VTI), BelgradeThe glycidyl azide polymer (GAP), known as an energetic, thermally stable, low sensitive, hydroxyl-terminated prepolymer, was synthesized using different diol and triol initiator units. GAP was prepared by azidation of poly(epichlorohydrin) (PECH) with different polyol units in the polymer chain. PECH was obtained by cationic ring-opening polymerization of epichlorohydrin, with BF3-etherate as a catalyst and polyol as a co-catalyst. The synthesized polymers have been characterized using IR-spectroscopy, while the prepolymers structure was confirmed by proton NMR spectroscopy. Additionally, glass transition temperature (Tg) and sensitivity to thermal stimuli were determined. Physico-chemical and rheological performances were carried out towards: end groups analysis, as well as density and molecular mass determination.https://scindeks-clanci.ceon.rs/data/pdf/1820-0206/2018/1820-02061802026N.pdfpolymerspolymer binderglycidyl azide polymerenergetic polymerschemical synthesismaterial propertiesphysico-chemical performances
collection DOAJ
language English
format Article
sources DOAJ
author Nešić Jovica
Marinković Aleksandar
Bajić Zoran
Brzić Saša
spellingShingle Nešić Jovica
Marinković Aleksandar
Bajić Zoran
Brzić Saša
Synthesis and characterization glycidyl azide polymer of an attractive binder for energetic materials
Scientific Technical Review
polymers
polymer binder
glycidyl azide polymer
energetic polymers
chemical synthesis
material properties
physico-chemical performances
author_facet Nešić Jovica
Marinković Aleksandar
Bajić Zoran
Brzić Saša
author_sort Nešić Jovica
title Synthesis and characterization glycidyl azide polymer of an attractive binder for energetic materials
title_short Synthesis and characterization glycidyl azide polymer of an attractive binder for energetic materials
title_full Synthesis and characterization glycidyl azide polymer of an attractive binder for energetic materials
title_fullStr Synthesis and characterization glycidyl azide polymer of an attractive binder for energetic materials
title_full_unstemmed Synthesis and characterization glycidyl azide polymer of an attractive binder for energetic materials
title_sort synthesis and characterization glycidyl azide polymer of an attractive binder for energetic materials
publisher Military Technical Institute, Belgrade
series Scientific Technical Review
issn 1820-0206
2683-5770
publishDate 2018-01-01
description The glycidyl azide polymer (GAP), known as an energetic, thermally stable, low sensitive, hydroxyl-terminated prepolymer, was synthesized using different diol and triol initiator units. GAP was prepared by azidation of poly(epichlorohydrin) (PECH) with different polyol units in the polymer chain. PECH was obtained by cationic ring-opening polymerization of epichlorohydrin, with BF3-etherate as a catalyst and polyol as a co-catalyst. The synthesized polymers have been characterized using IR-spectroscopy, while the prepolymers structure was confirmed by proton NMR spectroscopy. Additionally, glass transition temperature (Tg) and sensitivity to thermal stimuli were determined. Physico-chemical and rheological performances were carried out towards: end groups analysis, as well as density and molecular mass determination.
topic polymers
polymer binder
glycidyl azide polymer
energetic polymers
chemical synthesis
material properties
physico-chemical performances
url https://scindeks-clanci.ceon.rs/data/pdf/1820-0206/2018/1820-02061802026N.pdf
work_keys_str_mv AT nesicjovica synthesisandcharacterizationglycidylazidepolymerofanattractivebinderforenergeticmaterials
AT marinkovicaleksandar synthesisandcharacterizationglycidylazidepolymerofanattractivebinderforenergeticmaterials
AT bajiczoran synthesisandcharacterizationglycidylazidepolymerofanattractivebinderforenergeticmaterials
AT brzicsasa synthesisandcharacterizationglycidylazidepolymerofanattractivebinderforenergeticmaterials
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