Ordering of urchin-like charged copolymer micelles:: Electrostatic, packing and polyelectrolyte correlations

被引:53
作者
Muller, F [1 ]
Delsanti, M
Auvray, L
Yang, J
Chen, YJ
Mays, JW
Demé, B
Tirrell, M
Guenoun, P
机构
[1] CEA Saclay, Serv Phys Etat Condense, F-91191 Gif Sur Yvette, France
[2] CEA Saclay, Serv Chim Mol, F-91191 Gif Sur Yvette, France
[3] CEA Saclay, Lab Leon Brillouin, F-91191 Gif Sur Yvette, France
[4] Univ Alabama, Dept Chem, Birmingham, AL 35294 USA
[5] Inst Max Von Laue Paul Langevin, F-38042 Grenoble, France
[6] Univ Minnesota, Dept Chem Engn & Mat Sci, Minneapolis, MN 55455 USA
关键词
D O I
10.1007/s101890070040
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report the results of small-angle neutron scattering (SANS) studies on aqueous solutions of spherical polyelectrolyte micelles formed by association of charged-neutral diblock copolymers. The neutral moieties are found to self-assemble into small dense spheres (cores of the micelles) whose sizes are independent of the polymer concentration c. In the dilute regime, c < c*, where c* is the overlap concentration of the micelles, the conformation of the charged groups, which form the corona of the micelles, is found to be extended. A liquid-like order is observed over a wide concentration range spanning from the dilute regime to the concentrated regime. For c > c*, polyelectrolyte correlations appear at smaller spatial scales and coexist with the liquid-like order. These results suggest that for dense brushes, above c*, the rod-like statistics of the charged chains begin to disappear due to contraction of corona arms or by interpenetration of coronae. For less dense brushes, the charged chains are found to be extended up to concentrations far above c*, before the progressive development of polyelectrolyte correlations.
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页码:45 / 53
页数:9
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