Skip to main content
U.S. flag

An official website of the United States government

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Influence of Self-Assembly on Dynamical and Viscoelastic Properties of Telechelic Polymer Solutions

Published

Author(s)

D Bedrov, G D. Smith, Jack F. Douglas

Abstract

ncipient micellization in a model self-associating telechelic polymer solution results in a network with a transient elastic response that decays by a two-step relaxation: the first is due to a heterogeneous jump-diffusion process involving entrapment of end-groups within well-defined clusters and this is followed by rapid diffusion to neighboring clusters and a decay (terminal relaxation) due to cluster disintegration. The viscolelastic response of the solution manifests characteristics of a glass transition and an entangled polymer network.
Citation
Europhysics Letters
Volume
59
Issue
No. 3

Keywords

alpha-beta splitting, associating polymers, cluster formation, crossover temperature, entanglement, glass formation, michelle formation, telechelic, viscoelasticity

Citation

Bedrov, D. , Smith, G. and Douglas, J. (2002), Influence of Self-Assembly on Dynamical and Viscoelastic Properties of Telechelic Polymer Solutions, Europhysics Letters, [online], https://tsapps.nist.gov/publication/get_pdf.cfm?pub_id=851983 (Accessed July 18, 2024)

Issues

If you have any questions about this publication or are having problems accessing it, please contact reflib@nist.gov.

Created July 31, 2002, Updated October 12, 2021