Kinetics and mechanisms of the sphere-to-rod and rod-to-sphere transitionsin the ternary system PS310-b-PAA(52)/dioxane/water

Citation
Se. Burke et A. Eisenberg, Kinetics and mechanisms of the sphere-to-rod and rod-to-sphere transitionsin the ternary system PS310-b-PAA(52)/dioxane/water, LANGMUIR, 17(21), 2001, pp. 6705-6714
Citations number
86
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
LANGMUIR
ISSN journal
07437463 → ACNP
Volume
17
Issue
21
Year of publication
2001
Pages
6705 - 6714
Database
ISI
SICI code
0743-7463(20011016)17:21<6705:KAMOTS>2.0.ZU;2-Q
Abstract
The relaxation kinetics and transition mechanisms of the sphere-to-rod and rod-to-sphere transitions occurring in polystyrene-b-poly(acrylic acid) (PS -b-PAA) aggregates have been examined using solution turbidity measurements and transmission electron microscopy. The copolymer PS310-b-PAA(52) has be en found to self-assemble into aggregates with spherical, rodlike, and vesi cular shapes in dioxane-water mixtures. Recently, the morphological phase d iagram for this ternary system was constructed in order to determine the co ncentration boundaries associated with each aggregate architecture and the regions of morphological coexistence.(1) It had previously been found that a sudden alteration of the solvent composition near one of these boundaries could induce a morphological transition.(2) This approach has been used to investigate the kinetics and mechanisms of the sphere-to-rod and rod-to-sp here transitions. The transformation of spherical micelles to rodlike aggre gates occurs through a two-step mechanism; it begins with the fast, adhesiv e collisions of spheres resulting in the formation of irregular "pearl neck lace" intermediate structures. This is followed by the reorganization of th e necklace intermediates to form smooth rods. The rod-to-sphere transition also involves two steps. A bulb develops quickly on one or both ends of the rod, and then the bulbs are slowly pinched off to release free spheres in solution. The sphere-to-rod transition occurs at comparable rates to the re verse process. The effect of the jump magnitude, the initial solvent conten t, and the copolymer concentration on the relaxation rates was also investi gated.