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Thermal oxidative and photo-oxidative degradation of polytetrahydrofuran studied using ~1H NMR, ~(13)C NMR and GPC

机译:使用〜1H NMR,〜(13)C NMR和GPC研究聚四氢呋喃的热氧化降解和光氧化降解

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摘要

The products and mechanism of the thermal oxidative degradation at 180 °C and the photo-oxidative degradation at 40 °C of polytetrahydrofuran have been investigated using 1H NMR, ~(13)C NMR and GPC. The NMR analysis was assisted by the use of DEPT ~(13)C spectra, two-dimensional NMR spectroscopy (COSY, HMQC and HMBC) and chemical shift simulation software. The NMR spectra of both thermally and photolytically degraded samples were similar showing that the degradation mechanisms were similar. GPC indicated that both chain scission, leading to lower molar mass products, and chain extension, leading to higher molar mass products, occurred initially. NMR analysis of the initial soluble degraded polymers showed that chain scission resulted in formate, aldehyde, propyl ether, butyl ether and propanoyl chain ends, and in-chain ester groups were also formed. For longer periods of degradation, crosslinked gels were formed but these were not amenable to detailed structural characterisation by high-resolution NMR to determine the crosslink mechanism.
机译:使用1H NMR,〜(13)C NMR和GPC研究了聚四氢呋喃在180°C时的热氧化降解和40°C时的光氧化降解的产物和机理。使用DEPT〜(13)C光谱,二维NMR光谱(COSY,HMQC和HMBC)和化学位移模拟软件辅助NMR分析。热降解和光降解样品的NMR光谱相似,表明降解机理相似。 GPC指出,最初发生断链导致摩尔质量较低的产物,而延伸链导致摩尔质量较高的产物。初始可溶性降解聚合物的NMR分析表明,断链导致甲酸,醛,丙醚,丁醚和丙酰基链端基化,并且还形成了链内酯基。对于更长的降解时间,形成了交联的凝胶,但是这些凝胶不适合通过高分辨率NMR确定交联机理的详细结构表征。

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