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首页> 外文期刊>Journal of Applied Polymer Science >Isotactic poly(1-butene)/hydrogenated oligo(cyclopentadiene) blends: Miscibility, morphology, and thermal and mechanical properties
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Isotactic poly(1-butene)/hydrogenated oligo(cyclopentadiene) blends: Miscibility, morphology, and thermal and mechanical properties

机译:等规聚(1-丁烯)/氢化低聚(环戊二烯)共混物:混溶性,形态以及热力学性能

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The article discusses the influence of the oligomeric resin, hydrogenated oligo( cyclopentadiene) (HOCP), on the morphology and properties of its blends with isotactic poly(1-butene) (PB-1). PB-1 and HOCP are found to be partially miscible in the melt state. Solidified PB-1/HOCP blends contain three phases: (1) a crystalline phase formed by PB-1 crystals; (2) an amorphous PB-1-rich phase; and (3) an amorphous HOCP-rich phase. The optical micrographs of the solidified blends show a morphology constituted by microspherulites and domains of the HOCP-rich phase homogeneously distributed in the intraspherulitic region. DSC and DMTA results show two glass transition temperatures (T-g), different from the T-g values of the plain components. The lower T-g is attributed to the PB-1-rich phase, and the higher T-g, to the HOCP-rich phase. The tensile properties were investigated at 25 and 80 degrees C. At 25 degrees C, the PB-1-rich phase is rubbery and the HOCP-rich phase is glassy, so the addition of HOCP to PB-1 arouses a noteworthy hardening of the samples and this brings an increase of the Young's modulus, E' (although the blend crystallinity lessens), and decreases of stresses at yielding point (sigma(y)) and at rupture (sigma(r)). The 90/10 and 80/20 blends show high values of elongation at rupture (epsilon(r)). At 80 degrees C, the blends show decreases of E' and sigma(r) values with the HOCP content. These decreases are attributed to the rubbery state of the phases and reduction of the blend's crystallinity. At 80 degrees C, all the blends show a high value of epsilon(r). This phenomenon is attributed to the fine-size domain dispersion of the phases and to sufficient densities of tie molecules and entanglements. Finally, the partial miscibility behavior proposed in this article is compared with the miscibility hypothesis reported elsewhere. (C) 1998 John Wiley & Sons, Inc. [References: 25]
机译:本文讨论了低聚树脂氢化低聚(环戊二烯)(HOCP)对其与全同立构聚(1-丁烯)(PB-1)共混物的形态和性能的影响。发现PB-1和HOCP在熔融状态下可部分混溶。固化的PB-1 / HOCP共混物包含三个相:(1)由PB-1晶体形成的结晶相; (2)无定形PB-1富相。 (3)富含HOCP的非晶相。固化混合物的光学显微照片显示出由微球晶和均匀分布在球内区域的富含HOCP的相域组成的形态。 DSC和DMTA结果显示两个玻璃化转变温度(T-g),与普通组分的T-g值不同。较低的T-g归因于PB-1富集相,较高的T-g归因于HOCP富集相。在25和80摄氏度下研究了拉伸性能。在25摄氏度下,富含PB-1的相为橡胶状,富含HOCP的相为玻璃状,因此将PB-1加入HOCP引起了显着的硬化。样品,这会增加杨氏模量E'(尽管共混物结晶度降低),并且会降低屈服点(sigma(y))和断裂时的应力(sigma(r))。 90/10和80/20共混物在断裂时显示出很高的伸长率(ε)。在80摄氏度时,共混物显示HO'含量降低E'和sigma(r)值。这些降低归因于相的橡胶态和共混物结晶度的降低。在80摄氏度下,所有混合物均显示出较高的epsilon(r)值。该现象归因于相的精细尺寸的畴分散以及键分子和缠结的足够密度。最后,将本文中提出的部分混溶性行为与其他地方报道的混溶性假设进行了比较。 (C)1998 John Wiley&Sons,Inc. [参考:25]

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