Skip to main content

NOTICE: Due to a lapse in annual appropriations, most of this website is not being updated. Learn more.

Form submissions will still be accepted but will not receive responses at this time. Sections of this site for programs using non-appropriated funds (such as NVLAP) or those that are excepted from the shutdown (such as CHIPS and NVD) will continue to be updated.

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.

Lattice Model of Living Polymerization I. Basic Thermodynamic Properties

Published

Author(s)

J Dudowicz, Karl Freed, Jack F. Douglas

Abstract

A Flory-Huggins type model of living polymerization is formulated, incorporating chain stiffness, variable initiator concentration and polymer-polymer interactions. Basic equilibrium properties [average chain length L, average fraction of associated monomers diameter}, specific heat Cp, entropy S, and the chain length distribution p(N)] are calculated within mean-field theory. Our illustrative calculations are restricted to systems that polymerize upon cooling [e.g., poly(α-methylstyrene)], but the formalism also applies to polymerization upon heating (e.g., sulfur, actin). Emphasis is given to living solutions having a finite initiator concentration r in order to compare theory with recent experiments by Greer and coworkers, whereas previous primary focus on the r-> 0+ limit where the polymerization transition has been described as a second order phase transition. The general phenomena are analyzed in terms of three characteristic temperatures: a crossover temperature demarking the onset of polymerization, a polymerization temperature where Cp has a maximum, and a saturation temperature at which the extent of polymerization is almost complete. Paper 2 considers the interplay between polymerization and phase separation in living polymer solutions. Many of the properties of living polymers are representative of self-assembling systems (thermally reversible polymer gels, colloidal gels, micelles), and comparisons with other self-assembling systems are briefly indicated.
Citation
Journal of Chemical Physics
Volume
111
Issue
No.15

Keywords

associating polymer, gelation, glasses, living polymers, micelles

Citation

Dudowicz, J. , Freed, K. and Douglas, J. (1999), Lattice Model of Living Polymerization I. Basic Thermodynamic Properties, Journal of Chemical Physics, [online], https://tsapps.nist.gov/publication/get_pdf.cfm?pub_id=851616 (Accessed October 17, 2025)

Issues

If you have any questions about this publication or are having problems accessing it, please contact [email protected].

Created September 30, 1999, Updated October 12, 2021
Was this page helpful?