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Influence of the Processing Conditions on a Two-Phase Reactive Blend System: EVA/PP Thermoplastic Vulcanizate

机译:加工条件对两相反应共混体系的影响:EVA / PP热塑性硫化橡胶

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The elaboration of a TPV based on copolymer of ethylene and vinyl acetate (EVA) and polypropylene (PP) as thermoplastic phase was investigated in a batch mixer. The crosslinking reaction is carried out through a transesterification reaction between ester groups of EVA and alcoxysilane groups of the crosslinker agent tetrapropoxyorthosilicate (TPOS). The main advantage of this crosslinking reaction is that it can be well controlled and suitable for different processing conditions. The aim of the present study is to get a better understanding of the dispersion mechanism and of the phase inversion of the EVA major phase during its dynamic vulcanization into the PP minor phase. It was proved that the initial viscosity ratio, gamma = eta_(PP)/eta_(EVA), between EVA and PP plays an important part in the morphology development of the reactive blend. The viscosity ratio must be close to the critical ratio expressed by Utracki's model of phase inversion mechanism. Furthermore, the influence of different processing parameters on the variation of the morphology and on the mechanical properties of the ultimate TPV was investigated. The main conclusion of this study is that the characteristic time of crosslinking must be of the same order than the time of mixing. Indeed, better mechanical properties are obtained when a progressive phase inversion occurred and when it is controlled by rheological aspects and transient morphology equilibrium of the two phases and not by the mechanical fragmentation of the crosslinked EVA. For example, in our experimental conditions (concerning the amounts of catalyst and crosslinker reagents), high shear rates can be avoided (gamma < 80 s~(-1)) as the self-heating of the blend under shear considerably increases (DELTA T approx = 50 deg C for gamma = 225 s~(-1)), leading to faster kinetics and consequently to a phase inversion controlled by the fragmentation of the crosslinked EVA phase.
机译:在间歇混合器中研究了基于乙烯和醋酸乙烯酯(EVA)和聚丙烯(PP)的共聚物作为热塑性相的TPV的制备。交联反应通过EVA的酯基与交联剂四丙氧基原硅酸酯(TPOS)的烷氧基​​硅烷基之间的酯交换反应进行。该交联反应的主要优点是可以很好地控制并适合于不同的加工条件。本研究的目的是更好地了解EVA主相在动态硫化为PP小相期间的分散机理和相变。事实证明,EVA和PP之间的初始粘度比gamma = eta_(PP)/ eta_(EVA)在反应性共混物的形态发展中起重要作用。粘度比必须接近Utracki相转化机制模型所表达的临界比。此外,研究了不同加工参数对形态变化和最终TPV力学性能的影响。这项研究的主要结论是,交联的特征时间必须与混合时间相同。实际上,当发生渐进的相转化并且由流变学方面和两相的瞬时形态平衡而不是由交联的EVA的机械破碎控制时,可以获得更好的机械性能。例如,在我们的实验条件下(关于催化剂和交联剂的用量),可以避免高剪切速率(γ<80 s〜(-1)),因为在剪切作用下混合物的自热显着提高了(ΔT对于γ= 225 s〜(-1),约= 50摄氏度),从而导致动力学更快,并因此导致交联EVA相碎裂控制相转化。

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