Direct Surface Force and Contact Angle Measurements of an Adsorbed Polymer with a Lower Critical Solution Temperature
| Autor: | H. Ringsdorf, Jacob N. Israelachvili, Chad K. Park, J. Simon, F. J. Schmitt |
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| Rok vydání: | 1998 |
| Předmět: |
chemistry.chemical_classification
Chromatography Aqueous solution Comonomer Surface force Analytical chemistry Surface forces apparatus Surfaces and Interfaces Polymer Condensed Matter Physics Lower critical solution temperature Condensed Matter::Soft Condensed Matter Contact angle chemistry.chemical_compound chemistry Phase (matter) Electrochemistry General Materials Science Spectroscopy |
| Zdroj: | Langmuir. 14:2838-2845 |
| ISSN: | 1520-5827 0743-7463 |
| DOI: | 10.1021/la9709195 |
| Popis: | As an example of a polymer with a lower critical solution temperature, TLC, in water, we studied the phase behavior of a poly(N-isopropylacrylamide) copolymer. To adsorb it to a negatively charged surface, we introduced a positively charged comonomer. The combination of direct force measurements with the surface forces apparatus (SFA) and contact angle measurements reveal a lower TLC of the adsorbed layer than in bulk solution. At and above TLC the adsorbed polymer chains collapse and the adsorbed layers on the two opposing surfaces attract each other. The resulting adhesion is strongly dependent on the applied speed of separation, emphasizing the role of slow molecular relaxations and rearrangements above TLC. The results also point to the validity of the time−temperature superposition principle to this polymer system at T > TLC: at a low speed of separation the polymer layer is “liquid-like”, and at high speeds its behavior is more “solid-like”. |
| Databáze: | OpenAIRE |
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