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首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >EVA/PBT nanostructured blends synthesized by in situ polymerization of cyclic cBT (cyclic butylene terephthalate) in molten EVA
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EVA/PBT nanostructured blends synthesized by in situ polymerization of cyclic cBT (cyclic butylene terephthalate) in molten EVA

机译:EVA / PBT纳米结构共混物,通过在熔融EVA中原位聚合环状cBT(环状对苯二甲酸丁二酯)而合成

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摘要

Poly(ethylene-co-vinyl acetate) (EVA)/poly(butylene terephthalate) copolymers were synthesized by the in situ polymerization of cyclic butylene terephthalate monomer (cBT) in the presence of molten EVA copolymer. Titanium phenoxide Ti(OPh)(4) which leads to the highest degree of grafting compared to the more classical titanium system was used as the initiator for the ring-opening polymerization of the cBT monomer. The corresponding copolymer was characterized fully by H-1 NMR after selective extraction from the blend. As a result, a maximum of 11.3 wt% of EVA-g-PBT copolymer was synthesized by this method. Examination of morphology by transmission electronic microscopy (TEM) showed a fine dispersion of PBT phase with size ranging from 100 to 500 nm in diameter. This gave evidence for a crown structure of the PBT phase that is coated by EVA-g-PBT copolymer. Finally, theological and mechanical studies highlighted a specific behaviour of this material with improved mechanical properties at room temperature.
机译:通过在熔融的EVA共聚物的存在下,将对苯二甲酸丁二醇酯单体(cBT)原位聚合,合成了聚(乙烯-乙酸乙烯酯)(EVA)/聚对苯二甲酸丁二酯(共聚物)。与更经典的钛系统相比,可导致最高接枝度的苯氧基钛Ti(OPh)(4)被用作cBT单体开环聚合的引发剂。从共混物中选择性萃取后,相应的共聚物通过H-1 NMR充分表征。结果,通过该方法合成了最大11.3重量%的EVA-g-PBT共聚物。通过透射电子显微镜(TEM)检查形态,显示出PBT相的细分散,其直径范围为100至500nm。这提供了被EVA-g-PBT共聚物涂覆的PBT相的冠状结构的证据。最后,神学和力学研究强调了这种材料在室温下具有改善的机械性能的特定行为。

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