Thermo‐oxidative degradation of ultrahigh molecular weight poly(ethylene oxide) in volatile organic solvents

四氢呋喃 甲醇 激进的 傅里叶变换红外光谱 降级(电信) 氯仿 氯苯 环氧乙烷 材料科学 格式化 氧化物 乌贝洛德粘度计 光化学 有机化学 化学 高分子化学 特性粘度 化学工程 溶剂 催化作用 聚合物 工程类 电信 计算机科学 共聚物
作者
Shishun Bai,Kuo Chen,Wei Huang,Peng Wang,Xun Chen,Peng Chen
出处
期刊:Polymers for Advanced Technologies [Wiley]
卷期号:34 (2): 613-620 被引量:1
标识
DOI:10.1002/pat.5913
摘要

Abstract The degradation of ultrahigh molecular weight poly(ethylene oxide) (UHMWPEO) was investigated in three volatile organic solvents, methanol, chloroform, and tetrahydrofuran. Particularly, degradation rate was determined by means of Ubbelohde viscometry and degradation products were characterized by using electron spin resonance spectroscopy (ESR) and Fourier transform infrared spectroscopy (FTIR). The highest degradation rate was observed for UHMWPEO in tetrahydrofuran, with the lowest one in methanol. The ESR results showed that PEO‐C• and •OH radicals were produced during the degradation process. Among these selected solvents, tetrahydrofuran was found to generate free radicals through an autoxidation mechanism. This would accelerate the degradation of UHMWPEO, resulting in the observed highest degradation rate in the UHMWPEO/tetrahydrofuran solution. Esters were also detected in the degradation products of these UHMWPEO solutions, while formates and formate ions were generated in the solutions of UHMWPEO/tetrahydrofuran and UHMWPEO/cloroform except for PEO/methanol. Furthermore, the degradation mechanism of UHMWPEO was deduced. This work enabled an in‐depth understanding on the thermo‐oxidative degradation mechanism of UHMWPEO in representative organic solvents, which would be instructive for developing optimal solution‐based processing technique of UHMWPEO.

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