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Synthesis and bulk properties of poly(tetrahydrofuran)-poly(2-methyl-2-oxazoline) ABA triblock copolymers

机译:聚(四氢呋喃)-聚(2-甲基-2-恶唑啉)ABA三嵌段共聚物的合成及本体性能

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A series of linear triblock-copolymers of the ABA type in which the central B-block is poly(tetrahydrofuran) (polyTHF) and the A-segments are poly(2-methyl-2-oxazoline) (polyMeOX) were synthesized by a one-pot sequential monomer addition copolymerization, utilizing the living nature of the cationic ring-opening polymerization of both monomers. Films of the copolymers, casted from chloroform solutions, exhibit excellent mechanical properties in comparison with the homopolymers with comparable molecular weights, which was ascribed to the phase separation occurring between the two copolymer segments. Materials, in which the polyTHF B-segment have a molecular weight 13000 g/mol or higher and each polyMeOX A-block a molecular weight 1500 g/mol, kept elastomeric properties up to 130 degrees C notwithstanding the fact that this temperature is considerably higher than the melting point of polyTHF and the glass transition temperature of polyMeOX. It was found that these triblock-copolymer materials show a shape memory effect. These observations are attributed to the high degree of phase separation between the two blocks and the strong polar interactions between the polyMeOX segments.
机译:通过一个人合成了一系列的ABA型线性三嵌段共聚物,其中中心的B嵌段是聚四氢呋喃(polyTHF),而A段是聚(2-甲基-2-恶唑啉)(polyMeOX)。利用两种单体的阳离子开环聚合反应的活性,进行连续的单体加聚反应。与具有相当分子量的均聚物相比,由氯仿溶液浇铸的共聚物薄膜显示出优异的机械性能,这归因于两个共聚物链段之间发生的相分离。聚THF B链段的分子量为13000 g / mol或更高,而每个polyMeOX A嵌段的分子量为1500 g / mol的材料,尽管该温度要高得多,但仍可保持高达130摄氏度的弹性比聚THF的熔点和聚MeOX的玻璃化转变温度高。发现这些三嵌段共聚物材料显示出形状记忆效应。这些观察结果归因于两个嵌段之间的高度相分离以及polyMeOX链段之间的强极性相互作用。

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