Neutron scattering estimates of the effect of charge on the micelle structure in aqueous polyelectrolyte diblock copolymer solutions

Citation
W. Groenewegen et al., Neutron scattering estimates of the effect of charge on the micelle structure in aqueous polyelectrolyte diblock copolymer solutions, MACROMOLEC, 33(9), 2000, pp. 3283-3293
Citations number
36
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
MACROMOLECULES
ISSN journal
00249297 → ACNP
Volume
33
Issue
9
Year of publication
2000
Pages
3283 - 3293
Database
ISI
SICI code
0024-9297(20000502)33:9<3283:NSEOTE>2.0.ZU;2-O
Abstract
The dimension of spherical micelles of the diblock copolymer poly(styrene-b lock-acrylic acid) [PS(20)-b-PA(85)] was investigated as a function of the degree of ionization of the polyelectrolyte in the coronal layer. To descri be the structural arrangement of the blocks, the partial structure factors pertaining to PS-PS and PA-PA density correlations as well as the compositi on structure factor were obtained with small-angle neutron scattering and c ontrast matching in water. The PS blocks form a densely packed spherical co re with a radius 4.5 nm and an aggregation number similar to 100; the core structure does not depend on the corona charge to a significant degree. The extension of the PA chains in the coronal layer, and, hence, the micelle r adius, are found to be highly sensitive to the degree of ionization. At ful l ionization, the PA chains are almost fully stretched with a density scali ng proportional to the inverse second power of the radius away from the cor e. For lower charge fraction, the results are interpreted in terms of scali ng theory for star-branched polyelectrolytes, including the effects of char ge annealing. The dimension of the micelles was found to be controlled by t he balance of the elastic, conformational, stretching forces and the osmoti c pressure exerted by the counterions trapped within the corona.