Polymer Lateral Diffusion at the Solid−Liquid Interface
- 1 May 2004
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 126 (20) , 6242-6243
- https://doi.org/10.1021/ja0493749
Abstract
Measurements are presented of how polymer surface diffusion at the solid−liquid interface is controlled by surface coverage. The method of measurement was fluorescence correlation spectroscopy (FCS), and the system was poly(ethylene oxide) (PEG) adsorbed onto methyl-terminated self-assembled monolayers in buffered aqueous solution. The translational diffusion coefficient at first increased with increasing surface concentration, presumably because the number of adsorption sites per molecule decreased. Ultimately it slowed by 1 order of magnitude, presumably reflecting jamming by neighboring chains.Keywords
This publication has 15 references indexed in Scilit:
- Perspective: Kinetic and mechanical properties of adsorbed polymer layersThe European Physical Journal E, 2002
- Surface Diffusion of Poly(ethylene glycol)Macromolecules, 2002
- Casimir force in a critical film formed from an electrolytic solutionPhysical Review E, 2001
- DNA on Fluid Membranes: A Model Polymer in Two DimensionsMacromolecules, 2000
- Polymers interacting with spherical and rodlike particlesPhysical Review E, 1996
- Aggregative Behavior of Poly(ethylene oxide) in Water and MethanolMacromolecules, 1994
- Polyethylene oxide does not necessarily aggregate in waterNature, 1990
- Collapse of poly(ethylene oxide) monolayersMacromolecules, 1988
- Scaling theory of polymer adsorption : proximal exponentJournal de Physique Lettres, 1983
- Fluorescence correlation spectroscopy. II. An experimental realizationBiopolymers, 1974