Synthesis and characterization of novel energetic plasticizers based on poly glycidyl nitrate

增塑剂 玻璃化转变 热分解 差示扫描量热法 材料科学 高分子化学 傅里叶变换红外光谱 聚合 化学工程 化学 核化学 聚合物 有机化学 复合材料 工程类 物理 热力学
作者
Yadollah Bayat,Fatemeh Jozi,Tayebe Khanlari
出处
期刊:Journal of Energetic Materials [Informa]
卷期号:40 (2): 153-169 被引量:2
标识
DOI:10.1080/07370652.2020.1845874
摘要

Energetic plasticizers are used in propellants to increase the energy content and improve the glass transition temperature and mechanical properties. The compatibility between polymer and plasticizer is an important criterion for obtaining the best thermomechanical properties. In this research, novel energetic plasticizers were synthesized via end-group modification of poly glycidyl nitrate. Firstly, low molecular weight poly glycidyl nitrate (PGN) (Mn = 523 g.mol−1) and dinitropropyl poly glycidyl nitrate (DNPPGN) (Mn = 1700 g.mol−1) were synthesized by ring-opening polymerization of glycidyl nitrate with 1,4-butanediol and 2,2-dinitro-1,3-propanediol as initiators, respectively, and in the presence of boron trifluoride etherate (BF3.OEt2) as the catalyst. Tetra nitro poly glycidyl nitrate (TNPGN) was synthesized through end-group modification of DNPPGN and also azide-terminated GAP (GAPA) synthesized via modification of PGN as novel energetic plasticizers. The chemical structure of plasticizers was characterized by Fourier transform infrared spectroscopy (FT-IR) and nuclear magnetic resonance spectroscopy (NMR). Thermal behaviors were investigated by differential scanning calorimeter (DSC). The thermal analysis of plasticizers indicated Tg of TNPGN is lower than PGN and other synthesized plasticizers. Also, decomposition temperature (thermal stability) of TNPGN (251°C) is higher than PGN (209°C). Therefore, TNPGN has potential as a novel energetic plasticizer for propellant.
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