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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
Authors:Fábio A Bonk  Stefano Caldarelli  Trang Phan  Denis Bertin  Eduardo R Deazevedo  Gerson Luiz Mantovani  Tito J Bonagamba  Tomás S Plivelic  Iris L Torriani
Institution:1. Aix‐Marseille Université ISm2 UMR 6263, Site de Saint Jér?me, 13397 Cedex 20, Marseille, France;2. LCP UMR6264, Université de Provence, Site de Saint Jér?me, 13397, Marseille, France;3. Instituto de Física de S?o Carlos, Universidade de S?o Paulo, S?o Carlos SP, Brasil;4. Laboratório Nacional de Luz Síncrotron, Campinas SP, Brasil;5. Instituto de Física “Gleb Wataghin”, Universidade Estadual de Campinas, and Laboratório Nacional de Luz Síncrotron, Campinas SP, Brasil
Abstract: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
Keywords:ABA triblock‐copolymers  block copolymers  NMR  SAXS
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