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首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >Intermacromolecular complexation because of specific interactions 11. Ionic interaction complexation and its comparison with hydrogen-bonding complexation
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Intermacromolecular complexation because of specific interactions 11. Ionic interaction complexation and its comparison with hydrogen-bonding complexation

机译:由于特定的相互作用而导致大分子间的络合11.离子相互作用的络合及其与氢键络合的比较

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The ionic interaction complexation between metal carboxylated polystyrene ionomers and poly(butyl methacrylate-co-vinyl pyridine) (BVP) in both solution and bulk was studied by viscometry, laser light scattering (LLS) and differential scanning calorimetry (DSC) and compared with that between BVP and carboxylated polystyrene (CPS), in which the interacting groups are in acid form. The results show that both kinds of complexation strongly depend on the level of the specific interaction and give rise to an increased hydrodynamic radius over the component polymer coils. However, the ionic interaction complexation generally results in an increased viscosity in the solution and almost always exhibits two glass transition temperatures (T(g)s), in contrast, the hydrogen bonding complexation leads to a decreased viscosity and only one T-g. The different behavior is attributed to the difference in spatial distributions of the interacting sites in the complexes. (C) 2000 Elsevier Science Ltd. All rights reserved. [References: 33]
机译:通过粘度,激光散射(LLS)和差示扫描量热法(DSC)研究了金属羧化聚苯乙烯离聚物与聚(甲基丙烯酸丁酯-共乙烯基吡啶)(BVP)在溶液和本体中的离子相互作用的络合物并与之比较在BVP和羧化聚苯乙烯(CPS)之间形成相互作用,其中的相互作用基团为酸形式。结果表明,两种络合都强烈依赖于特定相互作用的水平,并导致组分聚合物线圈上的流体动力学半径增大。然而,离子相互作用络合通常导致溶液中的粘度增加,并且几乎总是表现出两个玻璃化转变温度(T(g)s),相反,氢键键合络合导致粘度降低,并且仅导致一个T-g。不同的行为归因于复合物中相互作用位点的空间分布的差异。 (C)2000 Elsevier ScienceLtd。保留所有权利。 [参考:33]

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