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Compositional effects on network structure of highly cross-linked copolymers of PEG-containing multiacrylates with acrylic acid

机译:组成成分对含PEG的聚丙烯酸酯与丙烯酸的高度交联共聚物网络结构的影响

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摘要

Novel ionizable polymer networks were prepared from oligo(ethylene glycol) (OEG) multiacrylates and acrylic acid (AA), employing bulk radical photopolymerization techniques. The properties of these materials exhibit a complex dependence on the network structure and composition. Dynamic mechanical analysis and penetrant sorption experiments demonstrated that the cross-linked structure of the materials depends very strongly on the AA content, even in cases where the network chain population is expected to be composed solely of ethylene glycol oligomers. The results indicate that interchain interactions are diminished as the AA content is increased, due to the increased spatial separation of OEG chains. The compositional dependence of the glass transition temperature is qualitatively described by a treatment consistent with that employed for polymer blends, and deviations from ideal blend behavior point to the importance of system-specific free volume changes during the radical polymerization process. Hence, the glass transition temperature and other network properties are closely coupled to the polymerization kinetics.
机译:采用本体自由基光聚合技术,由低聚乙二醇(OEG)聚丙烯酸酯和丙烯酸(AA)制备了新型可电离聚合物网络。这些材料的性能表现出对网络结构和组成的复杂依赖性。动态力学分析和渗透吸附实验表明,即使预期网络链总体仅由乙二醇低聚物组成,材料的交联结构也非常依赖于AA含量。结果表明,由于OEG链的空间间隔增加,随着AA含量的增加,链间相互作用减弱。玻璃化转变温度的成分依赖性通过与聚合物共混物所采用的处理一致的方法进行了定性描述,偏离理想共混物的行为表明了自由基聚合过程中系统特定自由体积变化的重要性。因此,玻璃化转变温度和其他网络性质与聚合动力学紧密相关。

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