双功能有机反离子中和的双相聚苯乙烯离聚体

L. Dulac, C. G. Bazuin
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引用次数: 6

摘要

通过比较双功能有机阳离子(即1,6-己二胺或HDA)中和的轻磺化聚苯乙烯(PS-SSA)离聚体与金属中和的双相离聚体的动态力学行为(作为离子含量和中和程度的函数),建立了双相形态的证据。hda中和离聚体的转变温度和强度随离子含量的变化趋势与金属中和离聚体,特别是聚苯乙烯基离聚体的转变温度和强度相似。在所研究的离子含量最高的PS-SSA-HDA离聚体上观察到一个小角度的x射线散射峰,称为“离聚体峰”。此外,观察到部分中和对簇相的影响比基体相更强烈。这可以解释为酸基团对基体Tg的贡献,以及它们在大量存在时影响离子相互作用强度或促进离子跳跃的能力,这主要影响簇Tg。
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Biphasic polystyrene ionomers neutralized by bifunctional organic counterions

The evidence for biphasic morphology in lightly sulfonated polystyrene (PS-SSA) ionomers neutralized by bifunctional organic cations (namely, 1,6-hexanediamine or HDA) is established by comparing their dynamic mechanical behavior, as a function of ion content and degree of neutralization, with that for metal-neutralized biphasic ionomers. The trends as a function of ion content regarding the transition temperatures and intensities of the HDA-neutralized ionomers parallel what is observed for metal-neutralized ionomers, in particular polystyrene-based ones. A small-angle X-ray scattering peak, identified as an “ionomer peak”, is observed in the PS-SSA-HDA ionomer of the highest ion content studied. Furthermore, it was observed that partial neutralization affects the cluster phase more strongly than the matrix phase. This can be explained by the contribution of the acid groups to the matrix Tg, and their ability, when present in large amounts, to affect the ionic interaction strength or facilitate ion hopping, which influences primarily the cluster Tg.

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