Thermal Treatment Effect on the Structure and Property Change between Hydroxy-Containing Polyimides (HPIs) and Thermally Rearranged Polybenzoxazole (TR-PBO)

聚合物 回转 热稳定性 回转半径 聚酰亚胺 热的 热处理 分子动力学 材料科学 体积热力学 化学 高分子化学 热力学 计算化学 纳米技术 复合材料 有机化学 几何学 物理 数学 图层(电子)
作者
Chi Hoon Park,Elena Tocci,Young Moo Lee,Enrico Drioli
出处
期刊:Journal of Physical Chemistry B [American Chemical Society]
卷期号:116 (42): 12864-12877 被引量:67
标识
DOI:10.1021/jp307365y
摘要

In this study, we report on the effect of thermal treatment on polyimide precursors (HPIs) and on the resulting thermally rearranged polybenzoxazole (TR-PBO) polymer membranes as investigated through the use of molecular dynamics (MD) simulations. For this purpose, we have first analyzed the structures of hydroxy-containing polyimides before thermal treatment and those of the thermally rearranged polybenzoxazoles after the thermal treatment, according to their temperature conditions. As expected, HPIs and TR-PBOs always show very limited motion of their polymer chains, indicated by the radius of gyration, due to their well-known thermal stability. In particular, the very rigid and stiff PBO linkages did not undergo significant change in their torsional angle distribution. On the other hand, in regards to intrachain movement, HPI chains were significantly affected by temperature. Their conformational changes were notably observed, which affected the distances between possible reaction sites, oxygen atoms in hydroxyl groups, and carbon atoms in the imido-ring. The free volume analysis, performed on both polymers and during thermal treatment, indicates that HPIs have a unimodal distribution of free volume areas, which partially coalesce in larger areas having, however, a relatively narrow size. Further, TR-PBO shows a bimodal cavity distribution, and after thermal treatment and TR reaction, the free volume structures in TR-PBO are maintained. The cavity size distributions determined by simulation were also consistent with free volume distributions determined by positron annihilation lifetime spectroscopy.
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