Molecular and morphological characterization of midblock‐sulfonated styrenic triblock copolymers |
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Authors: | Kenneth P. Mineart Justin J. Ryan Byeongdu Lee Steven D. Smith Richard J. Spontak |
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Affiliation: | 1. Department of Chemical & Biomolecular Engineering, North Carolina State University, Raleigh, North Carolina;2. Department of Materials Science & Engineering, North Carolina State University, Raleigh, North Carolina;3. Advanced Photon Source, Argonne National Laboratory, Argonne, Illinois;4. Corporate Research & Development, The Procter & Gamble Company, Cincinnati, Ohio |
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Abstract: | Midblock‐sulfonated triblock copolymers afford a desirable opportunity to generate network‐forming amphiphilic materials that are suitable for use in a wide range of emerging technologies as fuel‐cell, water‐desalination, ion‐exchange, photovoltaic, or electroactive membranes. Employing a previously reported synthetic strategy wherein poly(p‐tert‐butylstyrene) remains unreactive, we have selectively sulfonated the styrenic midblock of a poly(p‐tert‐butylstyrene‐b‐styrene‐b‐p‐tert‐butylstyrene) (TST) triblock copolymer to different extents. Comparison of the resulting sulfonated copolymers with results from our prior study provides favorable quantitative agreement and suggests that a shortened reaction time is advantageous. An ongoing challenge regarding the morphological development of charged block copolymers is the competition between microphase separation of the incompatible blocks and physical cross‐linking of ionic clusters, with the latter often hindering the former. Here, we expose the sulfonated TST copolymers to solvent‐vapor annealing to promote nanostructural refinement. The effect of such annealing on morphological characteristics, as well as on molecular free volume, is explored. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2017 , 55, 490–497 |
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Keywords: | block copolymers ionomers morphology TEM SAXS self‐assembly |
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