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Epoxy Networks with Physical Cross-Links Produced by Tail-to-Tail Associations of Alkyl Chains

机译:具有由烷基链的尾对尾关联产生的物理交叉链接的环氧树脂网络

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摘要

In a recent paper (Zucchi, I. A.; et al. Macromolecules 2008, 41, 4895), we showed that linear amphiphilic epoxy polymers synthesized by the polyaddition of diglycidyl ether of bisphenol A (DGEBA) with dodecylamine (DA)could undergo a physical gelation process through tail-to-tail association of dodecyl chains. The aim of the present study was to analyze in more detail conditions leading to the formation of epoxy networks with physical cross-links by the reaction of DGEBA with alkylamines of different chain lengths: octylamine (OA), dodecylamine (DA),and hexadecylamine (HA). SAXS spectra showed that tail-to-tail associations of alkyl chains were present since the beginning of polymerization and remained in the final materials. Initially, these associations correspond to micelles of the alkylamines dispersed in the solvent (DGEBA). Ill the Course of polymerization, micelles are disaggregated as the individual alkylamine chains become part of the linear amphiphilic polymer, However, tail-to-tail associations among alkyl chains attached to the polymer backbone persisted in the final materials. Reactions were followed by rheometry at 100 degrees C. For every system, it significant discontinuity in the increase in the storage modulus observed at advanced conversions was assigned to a phase inversion process produced by solvent depiction. By annealing prolonged times at the reaction temperature, a crossover of storage and loss modulus was observed because Of the increase in the extent of associations among alkyl chains leading to a physical gel. Times for physical gelation varied in the order OA < DA < HA. Both DGEBA-DA and DGEBA-HA polymers could be reversibly transformed from gel to liquid states by appropriate heating-cooling cycles; however, the DGEBA-OA polymer showed no thermoreversibility. Physical gels exhibited a high swelling capacity in THF (HA > DA > OA). These amphiphilic gels Could be used as dispersion media for a variety of nanoparticles stabilized with alkyl chains. They can also be the basis of single-component thermally remendable epoxy networks.
机译:在最近的一篇论文中(Zucchi,IA; et al.Macromolecules 2008,41,4895),我们表明通过双酚A的二缩水甘油醚(DGEBA)与十二烷基胺(DA)的加聚合成的线性两亲环氧聚合物可能会发生物理胶凝通过十二烷基链的尾到尾缔合过程。本研究的目的是更详细地分析导致DGEBA与不同链长的烷基胺(辛胺(OA),十二烷基胺(DA)和十六烷基胺(哈)。 SAXS光谱表明,自聚合开始以来,烷基链的尾到尾缔合一直存在,并保留在最终材料中。最初,这些缔合对应于分散在溶剂(DGEBA)中的烷基胺的胶束。在聚合过程中,随着单个烷基胺链成为线性两亲聚合物的一部分,胶束会分解。但是,连接到聚合物主链的烷基链之间的尾到尾缔合仍保留在最终材料中。在100℃下通过流变法跟踪反应。对于每个系统,在高级转化时观察到的储能模量增加的显着不连续性被归因于由溶剂描绘产生的相转化过程。通过在反应温度下长时间退火,观察到储存和损失模量的交叉,这是因为烷基链之间缔合程度的增加导致了物理凝胶。物理胶凝的时间以OA DA> OA)。这些两亲性凝胶可用作各种用烷基链稳定的纳米粒子的分散介质。它们也可以作为单组分可热固化环氧网络的基础。

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