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Effects of precursor origins on water sorption behaviors of various aromatic polyimides in thin films

机译:前体来源对薄膜中各种芳族聚酰亚胺水吸附行为的影响

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摘要

Poly(amic diethyl ester) [PAE] precursors of four different polyimides with various chain rigidities were synthesized and thermally converted to the polyimides in thin films: rodlike poly(p-phenylene pyromellitimide) [PMDA-PDA] and poly(4,4'-biphenylene pyromellitimide) [PMDA-BZ], pseudo-rodlike poly(p-phenylene biphenylenetetracarboximide) [BPDA-PDA] and semiflexible poly(4,4-oxydiphenylene pyromellitimide) [PMDA-ODA PAE]. For the polyimide films, water sorption behaviors were investigated by gravimetry and then compared with those of the polyimides prepared from the corresponding poly(amic acid) [PAA] precursors. In addition, their morphological structures were examined by X-ray diffraction. For all the polyimide, both water sorption and morphological structure were dependent upon the history of precursor origin. All the polyimides except PMDA-ODA revealed relatively higher diffusion coefficient of water, higher water sorption, lower intermolecular packing order and lower population of a more ordered phase in the PAE-derived polyimide films than the corresponding PAA-derived polyimide films. for PMDA-ODA, the variations in the water diffusion and sorption due to the precursor origin were relatively small in spite of a relatively large change in the morphological structure. Overall, the effect of precursor origin on the water diffusion and sorption is significantly high in the rodlike or pseudo-rodlike polyimides having a high chain rigidity and high intermolecular packing order, but relatively low in the semiflexible polyimide with a relatively low chain rigidity. In comparison, regardless of the precursor origins, the diffusion coefficient of water was in the decreasing order PMDA-ODA > PMDA-PDA > PMDA-BZ > BPDA-PDA and, however, the water sorption was in the decreasing order PMDA-PDA > PMDA-BZ > PMDA-ODA > BPDA-PDA. These water diffusion and sorption behaviors were understood by considering their chemical affinities to water in addition to the morphological structures.
机译:合成了四种具有不同链刚性的聚酰亚胺的聚酰胺二酰胺[PAE]前体,并将其热转化为薄膜中的聚酰亚胺:棒状聚对苯二甲基均苯四甲酰亚胺[PMDA-PDA]和聚(4,4' -联苯亚甲醛均苯四甲酰亚胺[PMDA-BZ],伪杆状聚(对苯撑亚联苯四甲酰亚胺)[BPDA-PDA]和半柔性聚(4,4-氧联二苯均苯四甲酰亚胺)[PMDA-ODA PAE]。对于聚酰亚胺膜,通过重量分析法研究其吸水性能,然后将其与由相应的聚(酰胺酸)[PAA]前体制备的聚酰亚胺进行比较。另外,通过X射线衍射检查了它们的形态结构。对于所有的聚酰亚胺,吸水率和形态结构都取决于前驱物的起源。与相应的PAA衍生的聚酰亚胺薄膜相比,除PMDA-ODA以外的所有聚酰亚胺在PAE衍生的聚酰亚胺薄膜中均显示出相对较高的水扩散系数,较高的吸水率,较低的分子间堆积顺序和较低的更有序相的种群。对于PMDA-ODA,尽管形态结构变化较大,但由于前驱物来源而引起的水扩散和吸附变化较小。总的来说,在具有高链刚性和高分子间堆积顺序的棒状或伪棒状聚酰亚胺中,前体起源对水扩散和吸附的影响显着高,而在具有相对低链刚性的半柔性聚酰亚胺中,前体起源对水的扩散和吸附的影响显着高。相比之下,无论前驱物的来源如何,水的扩散系数按降序排列PMDA-ODA> PMDA-PDA> PMDA-BZ> BPDA-PDA,但是,吸水率按降序排列PMDA-PDA> PMDA-BZ> PMDA-ODA> BPDA-PDA。除了形态结构外,还应考虑它们对水的化学亲和性,从而了解这些水的扩散和吸附行为。

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