Physico-chemical investigation of multiple asymmetric amphiphilic diblock copolymer morphologies in solution

Citation
S. Burke et A. Eisenberg, Physico-chemical investigation of multiple asymmetric amphiphilic diblock copolymer morphologies in solution, HIGH PERF P, 12(4), 2000, pp. 535-542
Citations number
36
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
HIGH PERFORMANCE POLYMERS
ISSN journal
09540083 → ACNP
Volume
12
Issue
4
Year of publication
2000
Pages
535 - 542
Database
ISI
SICI code
0954-0083(200012)12:4<535:PIOMAA>2.0.ZU;2-7
Abstract
Asymmetric amphiphilic diblock copolymers are able to form self-assembled c rewcut aggregates of multiple morphologies in selective solvents. Micelles are formed by the slow addition of a poor solvent, for the core-forming blo ck, to a solution of the copolymer dissolved in a solvent suitable for both polymer segments. The morphology of the aggregates is affected by a number of factors, such as the solvent composition, the block lengths, the presen ce of additives, and the temperature. Some of the resulting structures are considered to be equilibrium or near-equilibrium morphologies, which can be kinetically frozen using a number of different techniques. The thermodynam ics of micelle formation has been investigated, and equations for the stand ard Gibbs free energy, enthalpy, and entropy have been formulated. Partial phase diagrams have been constructed, giving the morphological phase bounda ries. Knowledge of the location of the boundaries has paved the way for the study of the kinetics and mechanisms of the sphere to rod and rod to vesic le transitions. Both processes have two-step mechanisms, with the second st ep being rate determining in each case.