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Property enhancements due to the in situ formation of fine-scale extended structures by chaotic mixing of polymer melts.

机译:由于通过聚合物熔体的混沌混合原位形成小规模的延伸结构,从而提高了性能。

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Chaotic mixing was employed in this study as a specially effective means to directly develop various fine-scale structures in polymer blends during melt processing. Three-dimensional chaotic advection was induced in melts within a cylindrical mixing cavity in response to the alternate motions of cavity surfaces. The emergent fine-scale extended structures in melts were subsequently captured upon solidification and mechanical properties were measured for different degrees of microstructure development.; The minor phase morphology developed during chaotic mixing was novel and distinctly different from those obtained by conventional processing techniques. In blends where interfacial tension was negligible, very thin sheets with numerous folds were generated. The thickness of the sheets decreased exponentially with processing time. In blends where interfacial tension was influential, lamellae were transformed to fibrils and later to droplets. The morphology development was documented by both optical and electron microscopy. Compared to the rapid breakdown of minor phase pellets into highly dispersed droplets which occurs in conventional batch mixing or extrusion, the structural development in melts during chaotic mixing was a gradual and progressive process and could be influenced by judicious manipulation of mixing conditions.; Impact tests were performed for 9 vol% LDPE/PS blends. Results demonstrated that very different impact properties in association with different microstructures were obtained for different mixing times. Lamellar structures were produced shortly after mixing began. These structures provided high impact toughness and long fracture times. When mixing was performed for considerably longer times, fine-scale fibrillar structures arose which provided greater strength and rigidity under impact. Tensile tests were carried out on blends consisting of a 10 vol% LCP minor phase and a PEN matrix. Electron microscopic examinations revealed that fibrils with diameters less than 10 {dollar}mu{dollar}m and aspect ratios up to 300 were produced after a short mixing time. Further mixing resulted in refinement of the fibrillar structures, and consequently significant enhancements in tensile properties.; The mechanisms of in-situ formation of fine-scale extended structures that this study has revealed may be useful in modifying or designing melt processing devices so that blends with favorable microstructures and improved properties can be produced.
机译:在这项研究中,采用混沌混合作为一种特别有效的手段,可以在熔体加工过程中直接开发出聚合物共混物中的各种精细结构。响应于型腔表面的交替运动,在圆柱形混合型腔内的熔体中引发了三维混沌对流。熔体中出现的细小扩展结构随后在凝固时被捕获,并针对不同程度的微结构发展测量了机械性能。混沌混合过程中形成的次要相形态是新颖的,并且与通过常规加工技术获得的形态明显不同。在界面张力可忽略不计的共混物中,产生了具有许多折痕的非常薄的片材。片材的厚度随处理时间呈指数下降。在界面张力影响较大的混合物中,薄片会转变为原纤维,然后转变为液滴。光学和电子显微镜都记录了形态学的发展。与常规分批混合或挤压过程中将次要相颗粒快速分解成高度分散的液滴相比,在混沌混合过程中,熔体的结构发展是一个渐进的过程,并可能受到对混合条件的明智操纵的影响。针对9体积%的LDPE / PS共混物进行了冲击测试。结果表明,对于不同的混合时间,获得了与不同的微观结构相关的非常不同的冲击性能。混合开始后不久便产生了层状结构。这些结构提供了高冲击韧性和长断裂时间。当混合进行相当长的时间时,出现了细尺度的原纤维结构,其在冲击下提供了更大的强度和刚度。对由10%(体积)LCP次要相和PEN基质组成的混合物进行拉伸试验。电子显微镜检查表明,在短时间混合后,产生了直径小于1010μm且长径比高达300的原纤维。进一步混合导致纤维状结构的细化,并因此显着提高了拉伸性能。这项研究表明,原位形成的细尺度延伸结构的机制可能有助于修改或设计熔体加工设备,从而可以生产出具有良好微观结构和改善性能的共混物。

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