首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >Confined crystallization phenomena in immiscible polymer blends with dispersed micro- and nanometer sized PA6 droplets,part 2:reactively compatibilized PS/PA6 and (PPE/PS)/PA6 blends
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Confined crystallization phenomena in immiscible polymer blends with dispersed micro- and nanometer sized PA6 droplets,part 2:reactively compatibilized PS/PA6 and (PPE/PS)/PA6 blends

机译:具有分散的微米和纳米级PA6小滴的不混溶聚合物共混物中的受限结晶现象,第2部分:反应相容的PS / PA6和(PPE / PS)/ PA6共混物

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In this paper the relation between the blend phase morphology and the fractionated crystallization behavior of PA6 in reactively compatibilized immiscible PS/PA6 and (PPE/PS)/PA6 immiscible blends is studied.Reactive compatibilization is used as an effective tool for controlling the blend phase morphology,and to reduce the PA6 dispersed droplet size.As reactive compatibilizers,SMA2 and SMA17 are used,which differ in their level of miscibility with the amorphous PS and (PPE/PS) components.With SMA2 a strong shift of PA6 crystallization to much higher supercoolings than before is found after compatibilization resulting in crystallization at temperatures as low as 85degC.This is ascribed to the strong decrease of the droplet sizes down to 100-150 nm.Nucleation experiments show that heterogeneous bulk nucleation can be reintroduced in the submicron-sized PA6 droplets by adding enough nucleating agents of sufficient small size.The degree of fractionated crystallization is found to depend on the interface between PA6 droplets and surrounding medium,as it is influenced by vitrification of the matrix polymer and by the location of the compatibilizers SMA2 and SMA17.The method used for mixing the reactive compatibilizer with the blend components also affects the fractionated crystallization process.
机译:本文研究了共混相形态与PA6在反应相容的不相容PS / PA6和(PPE / PS)/ PA6不相容的共混物中分馏结晶行为之间的关系。反应性相容化是控制共混相的有效工具SMA2和SMA17作为反应性增容剂,它们与无定形PS和(PPE / PS)组分的相溶性不同。SMA2使PA6的结晶性向很大的方向移动。相容后在低至85°C的温度下会结晶,因此过冷度比以前高。这归因于液滴尺寸低至100-150 nm的强烈减小。成核实验表明,可以在亚微米级结构中重新引入异质体形核。通过添加足够小尺寸的成核剂来确定PA6液滴的大小。分馏的结晶程度取决于PA6液滴与周围介质之间的界面,受基质聚合物的玻璃化以及增容剂SMA2和SMA17的位置的影响。反应性增容剂与共混物组分的混合方法也会影响分馏结晶过程。

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