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Elaboration and Characterization of Poly(4-vinylpyridine-co-N,N dimethylacrylamide)/Poly(styrene-co-methacrylic acid) Interpolymer Complexes

机译:聚(4-乙烯基吡啶-co-N,N二甲基丙烯酰胺)/聚(苯乙烯-co-甲基丙烯酸)互聚物配合物的制备与表征

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摘要

Proton-donor poly(styrene-co-methacrylic acid) containing 8 mol % of methacrylic acid (PSMA8) and poly(N,N-dimethylacrylamide-co-4vinylpyridine) containing 20 mol % of 4-vinylpyridine (PDMA4VP20) containing two proton accepting sites of different strength were synthesized and characterized by different techniques.By simply mixing appropriate amounts of these copolymers in chloroform, interpolymer complexes were formed, while homogeneous phases were observed when PSMA8 was mixed to poly(N,N-dimethyl acrylamide) or poly(4-vinylpyridine) in the same solvent.Due to the presence of specific interactions that occurred between the copolymers, these interpolymer complexes exhibited a single Tg in the whole composition range, higher than those calculated from the weight average values of the pure copolymers.The Tg-composition curves of these three systems, analyzed using Brostow et al. (BCKV) equation, confirmed from the high a0 values, obtained with PSMA8/PDMA4VP20 that the presence of 4VP units in PDMA4VP copolymers increased the average strength of intermolecular hydrogen bonding in the PDMA4VP20/PSMA8 systems compared to PDMA/PSMA8 or PSMA8/P4VP blends due to a higher number and stronger efficient specific interactions. Competing specific interactions of different strength carboxyl-pyridine, carboxylamide and carboxyl-carboxyl that occurred within these systems were evidenced by FTIR spectroscopy.
机译:含8摩尔%甲基丙烯酸(PSMA8)的质子给体聚(苯乙烯-甲基丙烯酸共聚物)和含20摩尔%含两个质子受体的4-乙烯基吡啶(PDMA4VP20)的聚(N,N-二甲基丙烯酰胺-共4乙烯基吡啶)通过将不同量的这些共聚物简单地混合在氯仿中,形成互聚物配合物,同时将PSMA8混合到聚(N,N-二甲基丙烯酰胺)或聚(在相同的溶剂中存在4-乙烯基吡啶)。由于共聚物之间存在特定的相互作用,因此这些共聚物配合物在整个组成范围内显示出一个单一的Tg,高于从纯共聚物的重均值计算得出的那些。使用Brostow等人分析的这三个系统的Tg组成曲线。 (BCKV)方程由PSMA8 / PDMA4VP20获得的高a0值证实,与PDMA / PSMA8或PSMA8 / P4VP共混物相比,PDMA4VP共聚物中4VP单元的存在增加了PDMA4VP20 / PSMA8系统中分子间氢键的平均强度由于数量更多且更有效的特定互动。 FTIR光谱证明了在这些系统中发生的不同强度的羧基吡啶,羧基酰胺和羧基羧基的竞争性特异性相互作用。

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