Tunable Morphologies From Bulk Self-Assemblies of Poly(acryloxypropyl triethoxysilane)-b-poly(styrene)-b-poly(acryloxypropyl triethoxysilane) Triblock Copolymers
Reactive poly(acryloxypropyl triethoxysilane)‐b‐poly(styrene)‐b‐poly(acryloxypropyl triethoxysilane) (PAPTES‐b‐PS‐b‐PAPTES) triblock copolymers are prepared through nitroxide‐mediated polymerization (NMP). The bulk morphologies formed by this class of copolymers cast into films are examined by small...
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Veröffentlicht in: | Macromolecular chemistry and physics 2012-01, Vol.213 (1), p.10-18 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Reactive poly(acryloxypropyl triethoxysilane)‐b‐poly(styrene)‐b‐poly(acryloxypropyl triethoxysilane) (PAPTES‐b‐PS‐b‐PAPTES) triblock copolymers are prepared through nitroxide‐mediated polymerization (NMP). The bulk morphologies formed by this class of copolymers cast into films are examined by small‐angle X‐ray scattering (SAXS) and transmission electron microscopy (TEM). The films morphology can be tuned from spherical structures to lamellar structures by increasing the volume fraction of PS in the copolymer. Thermal annealing at temperatures above 100 °C provides sufficient PS mobility to improve ordering.
The morphology of poly(acryloxypropyl triethoxysilane‐b‐styrene‐b‐acryloxy‐propyltriethoxysilane) copolymers (PAPTES‐ b‐PS‐b‐PAPTES) can be tuned from spherical structures to lamellar structures by increasing the volume fraction of PS in the copolymer from 13.0% to 43.7%. |
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ISSN: | 1022-1352 1521-3935 |
DOI: | 10.1002/macp.201100507 |