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Synthesis and structure-property relationships of polypropylene-g- poly(ethylene-co-1-butene) graft copolymers with well-defined long chain branched molecular structures

机译:具有明确的长链支链分子结构的聚丙烯-g-聚(乙烯-共-1-丁烯)接枝共聚物的合成及结构性质关系

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A series of polypropylene-g-poly(ethylene-co-1-butene) (PP-g-EBR) graft copolymers with well-defined long chain branched (LCB) molecular structures were synthesized via the combination of coordination polymerization and anionic polymerization. The structure-property relationships of PP-g-EBR were systematically investigated. The structural information was clarified by characterization of 1H NMR and SEC equipped with triple detectors. The DMA measurements demonstrated that the amorphous EBR branches were miscible with the PP backbones. The melt behavior of the PP-g-EBRs was studied with small-amplitude dynamic rheological measurements. Increasing branch length and branch density both led to increased zero-shear viscosity, more pronounced shear-thinning behavior, elevated value of storage modulus at low shear frequencies, more significant upshift deviation from linear behavior in the Han plot, and reduced loss angle. Comparatively, branch length contributed more to the improvement of rheological properties than branch density did. Interestingly, DSC results showed that the crystallization temperature of PP-g-EBR increased with the enhancement of branch length and branch density; however, when the LCB level exceeded a certain degree, further increasing the LCB level would reduce the crystallization temperature.
机译:通过配位聚合和阴离子聚合相结合,合成了一系列具有明确的长支链(LCB)分子结构的聚丙烯-g-聚(乙烯-co-1-丁烯)(PP-g-EBR)接枝共聚物。系统地研究了PP-g-EBR的结构-性质关系。结构信息通过配备三重检测器的1 H NMR和SEC的表征得到澄清。 DMA测量表明,无定形EBR支链可与PP主链混溶。 PP-g-EBRs的熔融行为通过小幅度动态流变学测量进行了研究。支链长度和支链密度的增加均导致零剪切粘度增加,剪切变稀行为更加明显,在低剪切频率下储能模量值升高,在Han曲线中线性行为的上移偏差更大,损耗角减小。相比之下,分支长度比分支密度对流变性能改善的贡献更大。有趣的是,DSC结果表明PP-g-EBR的结晶温度随着支链长度和支链密度的增加而增加。但是,当LCB含量超过一定程度时,进一步提高LCB含量会降低结晶温度。

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