z-logo
open-access-imgOpen Access
Polymerization-induced phase separation
Author(s) -
J. C. Lee
Publication year - 1999
Publication title -
physical review. e, statistical physics, plasmas, fluids, and related interdisciplinary topics
Language(s) - English
Resource type - Journals
eISSN - 1095-3787
pISSN - 1063-651X
DOI - 10.1103/physreve.60.1930
Subject(s) - monomer , polymerization , materials science , polymer , liquid crystal , chemical physics , molecule , kinetics , exponent , crystal (programming language) , phase (matter) , thermodynamics , entropy (arrow of time) , chemical engineering , organic chemistry , chemistry , composite material , physics , linguistics , philosophy , optoelectronics , quantum mechanics , computer science , programming language , engineering
A molecular dynamics simulation is performed to study the kinetics of microphase separation in a polymer-dispersed-liquid-crystal forming process. An equimolar mixture of monomers and liquid crystal molecules are thermalized in a well mixed state. The monomers are then polymerized at the same temperature. The end product is a spanning gel with liquid crystal molecules aggregating in droplets here and there. The peak position of the equal-time structure function suggests that the growth of the droplets may be described with t(-0.23). The small growth exponent is just one of several features which may be attributed to the growing elastic gel. We argue that the aggregation is driven by entropy.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom