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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Military Technical Institute, Belgrade
2018-01-01
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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 |
_version_ |
1724612953245745152 |