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首页> 外文期刊>Macromolecules >Origin of Multiple Melting Endotherms in a High Hard Block Content Polyurethane.2.Structural Investigation
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Origin of Multiple Melting Endotherms in a High Hard Block Content Polyurethane.2.Structural Investigation

机译:高硬嵌段含量聚氨酯中多次熔融吸热的起源2.结构研究

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The structure and morphology of a set of high hard block content(50% to 100% hard segment by weight)linear thermoplastic polyurethanes has been investigated mainly via small angle X-ray scattering(SAXS)and transmission electron microscopy(TEM).All the results obtained in this investigation have been correlated to our previous work on the thermodynamic properties of the same set of samples(Sainani et al.Macromolecules 2001,34,9059).The soft segment was based on a poly(propylene oxide)polyol end-capped with ethylene oxide and the hard segment on a 4,4'-methylenediphenyleneisocyanate(MDI)chain extended by 2-methyl-1,3-propanediol(MP-Diol).Samplex with a hard segment volume fraction higher than 65% are shown to have a morphology consisting in soft phase domains embedded in a hard phase matrix.Alignment of the soft phase domains could be observed under specific preparation conditions.From our SAXS results,the same average interdomaindistance was found for all the samples(d_1=15 nm).These results confirm our DSC results and suggest a two-phase structure for the melt-quenched samples:"pure"hard segment phase + mixed phase(soft+hard segments)with a hard segment content of 65 wt %.The mixed phase then undergoes phase separation during the annealing at 120 deg C.The dynamics of the phase separation was also investigated showing a strong correlation between the peak observed in the scattering curves and the so-called T_MMT melting endotherm.The results confirm the assignment of this endotherm to the microphase mixingof the soft and hard segments.The rate of phase separation was found to be a function of the hard segment content of the samples,and a delay time was found before the start of the phase separation process for the high hard block content samples.The degree of phase separation was calculated and found to be the same for all the samples except the PU-50%HS sample,which showed a higher degree of phase separation.The interface thickness is found to increase with increasing hard segment content.
机译:主要通过小角度X射线散射(SAXS)和透射电子显微镜(TEM)研究了一组高硬嵌段含量(按重量计为50%至100%的硬链段)的结构和形态。在这项研究中获得的结果与我们先前对同一组样品的热力学性质的研究相关(Sainani et al.Macromolecules 2001,34,9059)。软链段基于聚环氧丙烷多元醇末端用环氧乙烷封端并在由2-甲基-1,3-丙二醇(MP-Diol)延伸的4,4'-亚甲基二亚苯基异氰酸酯(MDI)链上的硬链段显示了硬链段体积分数高于65%的复合物在特定的制备条件下可以观察到软相域的排列。根据我们的SAXS结果,所有样品(d_1 = 15 nm)都具有相同的平均域间距离)。这些结果证实了我们的DSC结果,并提出了熔融淬火样品的两相结构:“纯”硬链段相+硬链段含量为65 wt%的混合相(软+硬链段)。在120℃退火过程中的分离过程。还研究了相分离的动力学,表明在散射曲线中观察到的峰与所谓的T_MMT熔化吸热之间有很强的相关性。结果证实了该吸热与微相有关发现相分离的速率是样品中硬段含量的函数,并且对于高含量的硬嵌段样品,在相分离过程开始之前发现了一个延迟时间。计算出相分离度,发现除PU-50%HS样品外所有样品的相分离度均相同,这表明相分离度更高。发现界面厚度随增加而增加细分内容。

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