Kurima Akihiro, Kinashi Kenji, Sakai Wataru, Tsutsumi Naoto
Doctor's Program of Materials Chemistry, Graduate School of Science and Technology, Kyoto Institute of Technology, Matsugasaki Sakyo, Kyoto 606-8585, Japan.
Platform Laboratory for Science & Technology, Asahi-Kasei Corporation, Moriyama City 524-0002, Japan.
Polymers (Basel). 2022 Nov 5;14(21):4748. doi: 10.3390/polym14214748.
The radical mechanisms of the thermal degradation of polyamide 66 (PA66) occurring under a vacuum at a temperature range between 80 °C and 240 °C (which includes the temperature of practical applications) were investigated using a spin-trapping electron spin resonance (ST-ESR) technique, as well as FTIR, TG-DTA, and GPC methods. No significant weight loss and no sign of thermal degradation are observed at this temperature range under oxygen-free conditions, but a slight production of secondary amine groups is confirmed by FTIR. GPC analysis shows a small degradation by the main chain scission. ST-ESR analysis reveals two intermediate radicals which are produced in the thermal degradation of PA66: (a) a CH- radical generated by main chain scission and (b) a -CH- radical generated by hydrogen abstraction from the methylene group of the main chain. The ST-ESR result does not directly confirm that a -NH-CH- radical is produced, although this reaction has been previously inferred as the initiation reaction of the thermal degradation of PA; however, the presence of -CH- radicals strongly suggests the occurrence of this initiation reaction, which takes place on the α-carbon next to the NH group. The ST-ESR analysis reveals very small levels of reaction, which cannot be observed by common analytical methods such as FTIR and NMR.
采用自旋捕获电子自旋共振(ST-ESR)技术以及傅里叶变换红外光谱(FTIR)、热重-差热分析(TG-DTA)和凝胶渗透色谱(GPC)方法,研究了聚酰胺66(PA66)在80℃至240℃温度范围内(涵盖实际应用温度)真空条件下发生热降解的自由基机理。在无氧条件下,此温度范围内未观察到明显的重量损失和热降解迹象,但FTIR证实有少量仲胺基团生成。GPC分析表明主链断裂导致了轻微降解。ST-ESR分析揭示了PA66热降解过程中产生的两种中间自由基:(a)主链断裂产生的CH·自由基,以及(b)从主链亚甲基上夺取氢产生的-CH·自由基。尽管先前已推断该反应为PA热降解的引发反应,但ST-ESR结果并未直接证实生成了-NH-CH·自由基;然而,-CH·自由基的存在强烈表明该引发反应的发生,该反应发生在NH基团旁边的α-碳上。ST-ESR分析揭示了极低水平的反应,这是FTIR和NMR等常规分析方法无法观察到的。