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羧化GAP共聚物的绿色合成与表征

Ecofriendly synthesis and characterization of carboxylated GAP copolymers.

作者信息

Kim Hancheul, Jang Yoorim, Noh Sitae, Jeong Jongoh, Kim Donghyun, Kang Byeongkwan, Kang Taewun, Choi Hyungtaek, Rhee Hakjune

机构信息

Department of Bionanotechnology, Hanyang University 55 Hanyangdaehak-ro Sangnok-gu, Ansan Gyeonggi-do 15588 South Korea

Department of Chemical Engineering, College of Engineering Sciences, Hanyang University 55 Hanyangdaehak-ro Sangnok-gu, Ansan Gyeonggi-do 15588 South Korea.

出版信息

RSC Adv. 2018 May 31;8(36):20032-20038. doi: 10.1039/c8ra03643h. eCollection 2018 May 30.

DOI:10.1039/c8ra03643h
PMID:35541650
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9080787/
Abstract

Carboxylated GAP copolymers (polyGA-carboxylate) compounds (1-7), were synthesized by the simultaneous substitution reaction with PECH, sodium azide, and sodium carboxylate in DMSO. The synthesized compounds (1-7) were characterized by various analysis tools, such as Fourier transform infrared (FT-IR), inverse gated decoupling C-nuclear magnetic resonance (C NMR), gel permeation chromatography (GPC), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), calorimetry, and friction and impact sensitivity. These poly(GA-carboxylate) compounds (1-7) have better thermal properties owing to their lower glass transition temperatures, from -48 °C to -55 °C, compared to glycidyl azide polymer (GAP) (-49 °C) and similar first thermal decomposition temperatures (228-230 °C) in comparison to GAP (227 °C), regardless of the introduction of the carboxylate group in GAP. Moreover, poly(GA-butyrate) and poly(GA-decanoate) have higher heats of combustion (2331 and 2976 kJ mol) and negative formation enthalpies (-0.75 and -2.02 kJ g), while GAP has a lower heat of combustion (2029 kJ mol) and positive formation enthalpy (1.33 kJ g). Therefore, poly(GA-carboxylate) could be a good candidate for the polymeric binder in solid propellants.

摘要

羧化GAP共聚物(聚GA - 羧酸盐)化合物(1 - 7)通过在二甲基亚砜(DMSO)中与聚环氧氯丙烷(PECH)、叠氮化钠和羧酸钠同时进行取代反应合成。合成的化合物(1 - 7)通过各种分析工具进行表征,如傅里叶变换红外光谱(FT - IR)、反门控去耦碳核磁共振(C NMR)、凝胶渗透色谱(GPC)、热重分析(TGA)、差示扫描量热法(DSC)、量热法以及摩擦和撞击感度。这些聚(GA - 羧酸盐)化合物(1 - 7)具有更好的热性能,这是由于它们的玻璃化转变温度较低,在 - 48℃至 - 55℃之间,相比缩水甘油叠氮聚合物(GAP)( - 49℃),并且与GAP(22)相比具有相似的初始热分解温度(228 - 230℃)。此外,聚(GA - 丁酸盐)和聚(GA - 癸酸盐)具有更高的燃烧热(2331和2976 kJ/mol)和负生成焓( - 0.75和 - 2.02 kJ/g),而GAP具有较低的燃烧热(2029 kJ/mol)和正生成焓(1.33 kJ/g)。因此,聚(GA - 羧酸盐)可能是固体推进剂中聚合物粘合剂的良好候选材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fedc/9080787/8e9799ca6d3a/c8ra03643h-f7.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fedc/9080787/e0e4696d31f8/c8ra03643h-f1.jpg
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