Volume 73, Number 2, January 2006
|Page(s)||204 - 210|
|Section||Atomic and molecular physics|
|Published online||02 December 2005|
Copolymer adsorption kinetics at a selective liquid-liquid interface: Scaling theory and computer experiment
Max-Planck-Institute for Polymer Research - Ackermannweg 10 55128 Mainz, Germany
2 Institute for Physical Chemistry, Bulgarian Academy of Sciences 1113 Sofia, Bulgaria
Corresponding author: email@example.com
Accepted: 9 November 2005
We consider the adsorption kinetics of a regular block copolymer of total length N and block size M at a selective liquid-liquid interface in the limit of strong localization. We propose a simple analytic theory based on scaling considerations which describes the relaxation of the initial coil into a flat-shaped layer. The characteristic times for attaining equilibrium values of the gyration radius components perpendicular and parallel to the interface are predicted to scale with chain length N and block length M as (here is the Flory exponent) and as , although the initial characteristic time of coil flattening is expected to grow with block size as . Since typically for multiblock copolymers, our results suggest that the flattening dynamics proceeds faster perpendicular rather than parallel to the interface. We also demonstrate that these scaling predictions agree well with the results of extensive Monte Carlo simulations of the localization dynamics.
PACS: 36.20.-r – Macromolecules and polymer molecules / 68.05.-n – Liquid-liquid interfaces / 07.05.Tp – Computer modeling and simulation
© EDP Sciences, 2006
Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.
Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.
Initial download of the metrics may take a while.