Cationic gel crystals of lightly cross-linked poly(2-vinylpyridine) spheres (170∼180 nm in diameter) in the deionized aqueous suspension

Colloidal crystallization of deionized suspensions of the cationic gel spheres of lightly cross-linked poly(2-vinylpyridine), AIBA-P2VP (170∼180 nm in diameter) has been studied from the microscopic observation, morphology, phase diagram, and elastic property. Critical concentrations of melting that coexisted with ion-exchange resins were low compared with those without resins and decreased as the degree of cross-linking decreased. The density of a gel sphere in suspension state (ρ), i.e., weight percent of the gel spheres divided by the corresponding volume percent, was between 0.5 and 0.8, and decreased as the degree of cross-linking of the spheres decreased. The ρ values also decreased with decreasing size of gel spheres, which supports the small P2VP gel spheres being softer than the large ones. The closest intersphere distances of the crystals were much longer than the hydrodynamic diameters of the gel spheres especially at low sphere concentrations. Fluctuation parameters evaluated from the rigidities of the crystals of AIBA-P2VP (0.05∼0.09) were similar to those of gel crystals of cationic gel spheres of lightly cross-linked poly(2-vinylpyridine) spheres coated with poly(ethylene glycol), 400 nm in diameter, and thermo-sensitive gel spheres of pNIPAm, poly(N-isopropylacrylamide), but larger than those of typical colloidal hard spheres. The stable crystal phase formed beyond the adsorbed monolayer of cationic gel spheres on the surface of the substrate. These experimental findings support important role of the extended electrical double layers around the cationic gel spheres in addition to the excluded volume effect of the sphere themselves on the crystallization.