Cargando…

Synthesis and characterization of carboxylated PBAMO copolymers as promising prepolymers for energetic binders

The carboxylated poly[3,3-bis(3-azidomethyl)oxetane] (PBAMO) copolymers (poly(BAMO-carboxylate)) were synthesized by substitution of poly[3,3-bis(3-chloromethyl)oxetane] (PBCMO) with potassium carboxylate and sodium azide in DMSO. The synthesized compounds were characterized using various analytical...

Descripción completa

Detalles Bibliográficos
Autores principales: Lim, Minkyung, Bu, Meilan, Jang, Yoorim, Jeong, Jongoh, Noh, Sitae, Rhee, Hakjune
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050039/
https://www.ncbi.nlm.nih.gov/pubmed/35496527
http://dx.doi.org/10.1039/c9ra09881j
_version_ 1784696277877915648
author Lim, Minkyung
Bu, Meilan
Jang, Yoorim
Jeong, Jongoh
Noh, Sitae
Rhee, Hakjune
author_facet Lim, Minkyung
Bu, Meilan
Jang, Yoorim
Jeong, Jongoh
Noh, Sitae
Rhee, Hakjune
author_sort Lim, Minkyung
collection PubMed
description The carboxylated poly[3,3-bis(3-azidomethyl)oxetane] (PBAMO) copolymers (poly(BAMO-carboxylate)) were synthesized by substitution of poly[3,3-bis(3-chloromethyl)oxetane] (PBCMO) with potassium carboxylate and sodium azide in DMSO. The synthesized compounds were characterized using various analytical techniques, such as Fourier-transform infrared (FT-IR) spectroscopy, inverse-gated decoupling (13)C-nuclear magnetic resonance ((13)C NMR) spectroscopy, gel permeation chromatography (GPC), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), calorimetry, friction, and impact sensitivity analysis. These poly(BAMO-carboxylate) compounds have better thermal properties, with lower glass transition temperatures (ranging from −43 °C to −51 °C) than PBAMO (−37 °C) and higher thermal decomposition temperatures (233–237 °C) than PBAMO (211 °C). Moreover, poly(BAMO(0.80)-octanoate(0.20)) and poly(BAMO(0.78)-decanoate(0.22)) have higher heats of combustion (5226 and 5665 kJ mol(−1), respectively) and negative formation enthalpies (−0.17 and −0.55 kJ g(−1), respectively), while PBAMO has lower heat of combustion (3125 kJ mol(−1)) and positive formation enthalpy (0.06 kJ g(−1)). The poly(BAMO-carboxylate) compounds have higher values (38–50 J) than that of PBAMO (14 J) in the impact sensitivities. This is a valuable study for improving the properties of PBAMO, which is a high energetic polymeric binder but difficult to handle because of its sensitivity. Therefore, poly(BAMO-carboxylate) could be a good candidate as a prepolymer for designing the energetic polymeric binder.
format Online
Article
Text
id pubmed-9050039
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher The Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-90500392022-04-29 Synthesis and characterization of carboxylated PBAMO copolymers as promising prepolymers for energetic binders Lim, Minkyung Bu, Meilan Jang, Yoorim Jeong, Jongoh Noh, Sitae Rhee, Hakjune RSC Adv Chemistry The carboxylated poly[3,3-bis(3-azidomethyl)oxetane] (PBAMO) copolymers (poly(BAMO-carboxylate)) were synthesized by substitution of poly[3,3-bis(3-chloromethyl)oxetane] (PBCMO) with potassium carboxylate and sodium azide in DMSO. The synthesized compounds were characterized using various analytical techniques, such as Fourier-transform infrared (FT-IR) spectroscopy, inverse-gated decoupling (13)C-nuclear magnetic resonance ((13)C NMR) spectroscopy, gel permeation chromatography (GPC), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), calorimetry, friction, and impact sensitivity analysis. These poly(BAMO-carboxylate) compounds have better thermal properties, with lower glass transition temperatures (ranging from −43 °C to −51 °C) than PBAMO (−37 °C) and higher thermal decomposition temperatures (233–237 °C) than PBAMO (211 °C). Moreover, poly(BAMO(0.80)-octanoate(0.20)) and poly(BAMO(0.78)-decanoate(0.22)) have higher heats of combustion (5226 and 5665 kJ mol(−1), respectively) and negative formation enthalpies (−0.17 and −0.55 kJ g(−1), respectively), while PBAMO has lower heat of combustion (3125 kJ mol(−1)) and positive formation enthalpy (0.06 kJ g(−1)). The poly(BAMO-carboxylate) compounds have higher values (38–50 J) than that of PBAMO (14 J) in the impact sensitivities. This is a valuable study for improving the properties of PBAMO, which is a high energetic polymeric binder but difficult to handle because of its sensitivity. Therefore, poly(BAMO-carboxylate) could be a good candidate as a prepolymer for designing the energetic polymeric binder. The Royal Society of Chemistry 2020-03-02 /pmc/articles/PMC9050039/ /pubmed/35496527 http://dx.doi.org/10.1039/c9ra09881j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Lim, Minkyung
Bu, Meilan
Jang, Yoorim
Jeong, Jongoh
Noh, Sitae
Rhee, Hakjune
Synthesis and characterization of carboxylated PBAMO copolymers as promising prepolymers for energetic binders
title Synthesis and characterization of carboxylated PBAMO copolymers as promising prepolymers for energetic binders
title_full Synthesis and characterization of carboxylated PBAMO copolymers as promising prepolymers for energetic binders
title_fullStr Synthesis and characterization of carboxylated PBAMO copolymers as promising prepolymers for energetic binders
title_full_unstemmed Synthesis and characterization of carboxylated PBAMO copolymers as promising prepolymers for energetic binders
title_short Synthesis and characterization of carboxylated PBAMO copolymers as promising prepolymers for energetic binders
title_sort synthesis and characterization of carboxylated pbamo copolymers as promising prepolymers for energetic binders
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050039/
https://www.ncbi.nlm.nih.gov/pubmed/35496527
http://dx.doi.org/10.1039/c9ra09881j
work_keys_str_mv AT limminkyung synthesisandcharacterizationofcarboxylatedpbamocopolymersaspromisingprepolymersforenergeticbinders
AT bumeilan synthesisandcharacterizationofcarboxylatedpbamocopolymersaspromisingprepolymersforenergeticbinders
AT jangyoorim synthesisandcharacterizationofcarboxylatedpbamocopolymersaspromisingprepolymersforenergeticbinders
AT jeongjongoh synthesisandcharacterizationofcarboxylatedpbamocopolymersaspromisingprepolymersforenergeticbinders
AT nohsitae synthesisandcharacterizationofcarboxylatedpbamocopolymersaspromisingprepolymersforenergeticbinders
AT rheehakjune synthesisandcharacterizationofcarboxylatedpbamocopolymersaspromisingprepolymersforenergeticbinders