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Investigation by combined solid-state NMR and SAXS methods of the morphology and domain size in polystyrene-b-polyethylene oxide-b-polystyrene triblock copolymers

机译:在聚苯乙烯-b-聚环氧乙烷-b-聚苯乙烯三嵌段共聚物中结合固态NmR和saXs方法研究形貌和畴尺寸

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摘要

The microphase structure of a series of polystyrene-b-polyethylene oxide-b-polystyrene (SEOS) triblock copolymers with different compositions and molecular weights has been studied by solid-state NMR, DSC, wide and small angle X-ray scattering (WAXS and SAXS). WAXS and DSC measurements were used to detect the presence of crystalline domains of polyethylene-oxide (PEO) blocks at room temperature as a function of the copolymer chemical composition. Furthermore, DSC experiments allowed the determination of the melting temperatures of the crystalline part of the PEO blocks. SAXS measurements, performed above and below the melting temperature of the PEO blocks, revealed the formation of periodic structures, but the absence or the weakness of high order reflections peaks did not allow a clear assessment of the morphological structure of the copolymers. This information was inferred by combining the results obtained by SAXS and 1H NMR spin diffusion experiments, which also provided an estimation of the size of the dispersed phases of the nanostructured copolymers. © 2009 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 48: 55–64, 2010
机译:通过固态NMR,DSC,宽角和小角X射线散射(WAXS和XRD)研究了一系列具有不同组成和分子量的聚苯乙烯-b-聚环氧乙烷-b-聚苯乙烯(SEOS)三嵌段共聚物的微相结构。 SAXS)。 WAXS和DSC测量用于检测室温下聚环氧乙烷(PEO)嵌段的晶域随共聚物化学组成的变化。此外,DSC实验允许确定PEO嵌段结晶部分的熔融温度。在PEO嵌段的熔融温度之上和之下进行的SAXS测量揭示了周期性结构的形成,但是高阶反射峰的缺失或弱点无法清晰评估共聚物的形态结构。通过结合SAXS和1H NMR自旋扩散实验获得的结果可以推断出此信息,这也提供了纳米结构共聚物分散相尺寸的估算值。 ©2009 Wiley Periodicals,Inc. J Polym Sci B部分:Polym Phys 48:55–64,2010年

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