Berlin 2005 – scientific programme
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CPP: Chemische Physik und Polymerphysik
CPP 29: POSTER: Polymer physics
CPP 29.13: Poster
Tuesday, March 8, 2005, 16:30–18:30, Poster TU D
Formation of Large PEE-Domains in PEE212−PEO112 Diblock Copolymer Monolayers: Shift of the PEO-Desorption Transition — •Alexander Wesemann1, Heiko Ahrens1, Stephan Förster2 und Christiane A. Helm1 — 1Angewandte Physik, Uni Greifswald, 17487 Greifwald — 2Physikalische Chemie, Uni Hamburg, 20146 Hamburg
PEE212−PEO112 diblock copolymer monolayers are studied at the air-water interface. At large molecular areas, with X-ray reflectivity PEE domains are observed, which are partly immersed into the water. The domain thickness increases on compression (28 to 40 Å). With off-specular X-ray reflectivity, an average domain radius of 750 Å is found, but there are also smaller domains. Due to the space constraints, most PEO-blocks form a brush beneath the PEE domains. Only a few PEO-blocks form a corona surrounding the domains and adsorb flatly onto the air-water interface. When the domain area fraction is 95%, the onset of the PEO desorption transition is found at the typical pressure of 9 mN/m. Yet, it occurs at 6 Å2/EO-monomer, 50 % of the value found usually. Apparently, the thickness of the PEE-domains is determined by the forces from the two interfaces, not by the PEO-block.