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Compatibilization of thermoplastic/silicone blends.

机译:热塑性/硅氧烷共混物的相容性。

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摘要

The melt blending of thermoplastic resins with silicones may offer beneficial property improvements. To achieve these benefits when the dispersed phase concentration is high (>20%), the blend morphology must be stabilized to prevent coalescence. Specifically, this thesis compares poly(styrene) (PS)/poly(dimethylsiloxane) (PDMS) blends stabilized with pre-made versus in situ reactively formed PS-PDMS block copolymers.;The high PS/PDMS immiscibility, comparatively low PDMS viscosity and limited quantities of model polymers required a small (<1 g), intense mixer. The dispersion of two blend systems, PS/poly(propylene) (PP) and PS/PDMS, was improved in a cup and rotor mixer (~0.5 g) by simply adding three steel balls. The PS/PP morphology was similar to that in larger mixers such as internal batch mixers and twin-screw extruders. The addition of the balls may have introduced elongational flows, higher shear rates and a wider range of deformation rates needed for effective particle break-up.;Model reactive PS and PDMS polymers were synthesized by anionic polymerization in order to more easily detect copolymer formation with gel permeation chromatography (GPC). Electron microscopy (scanning and transmission) was then used to observe the effect of reaction on morphology. In agreement with earlier work in other systems, the amine-anhydride reaction was much more effective in producing stable, small PDMS particles in PS compared to the carboxylic acid/epoxy or amine/epoxy reactions. The effectiveness of the amine/anhydride reaction was also suggested by the improved PDMS dispersion into commercial poly(caprolactam) (PA6) when the PDMS possessed pendant anhydride groups.;Pre-made symmetric PS-PDMS diblocks, were added to PS/PDMS blends. Instead of localizing at the interface, the block copolymer preferred to form micelles. The diffusion of block copolymer also limited the block copolymer's ability to reach the interface. The particle size was affected by the PS/PDMS viscosity ratio. When the viscosities were nearly matched, stable sub-micron dispersions of 20% PDMS in PS could be achieved using as little as 1% diblock. The improved dispersion may be attributed to better deformation of the phases or to changes in the interfacial tension as the molecular weight of the homopolymers or diblocks was varied.
机译:热塑性树脂与硅酮的熔融共混可以提供有益的性能改善。为了在分散相浓度高(> 20%)时获得这些好处,必须稳定共混物形态以防止聚结。具体而言,本文比较了用预制与原位反应形成的PS-PDMS嵌段共聚物稳定的聚苯乙烯(PS)/聚二甲基硅氧烷(PDMS)共混物.PS / PDMS的不溶混性高,PDMS的粘度较低和数量有限的模型聚合物需要使用小型(<1 g)的强力混合器。只需添加三个钢球,即可在杯形转子混合器(〜0.5 g)中改善PS /聚丙烯(PP)和PS / PDMS这两种共混体系的分散性。 PS / PP的形态与较大的混合机(例如内部间歇式混合机和双螺杆挤出机)相似。球的加入可能会引入伸长流,更高的剪切速率和更大的变形速率范围,从而有效地破坏了颗粒。阴离子聚合合成了模型反应性PS和PDMS聚合物,以便更轻松地检测与凝胶渗透色谱法(GPC)。然后使用电子显微镜(扫描和透射)观察反应对形态的影响。与其他系统中的早期工作相一致,与羧酸/环氧反应或胺/环氧反应相比,胺酐反应在PS中生产稳定的小PDMS颗粒要有效得多。当PDMS具有侧酸酐基团时,改进的PDMS在商业化聚己内酰胺(PA6)中的分散性也表明了胺/酸酐反应的有效性。将预制的对称PS-PDMS二嵌段添加到PS / PDMS共混物中。嵌段共聚物优选形成胶束,而不是定位在界面上。嵌段共聚物的扩散也限制了嵌段共聚物到达界面的能力。粒度受PS / PDMS粘度比的影响。当粘度接近匹配时,使用低至1%的二嵌段即可在PS中获得20%PDMS的亚微米稳定分散体。改进的分散性可归因于相的更好变形或随着均聚物或二嵌段的分子量的变化界面张力的变化。

著录项

  • 作者

    Maric, Milan.;

  • 作者单位

    University of Minnesota.;

  • 授予单位 University of Minnesota.;
  • 学科 Engineering Chemical.
  • 学位 Ph.D.
  • 年度 1999
  • 页码 182 p.
  • 总页数 182
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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