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Effects of Secondary Polymer Covalently Attached to Monodisperse, Poly(maleic anhydride–styrene)-Modified Colloidal Silica on Dispersibility in Organic Solvent

✍ Scribed by Kohji Yoshinaga; Junji Shimada; Hiroyasu Nishida; Michio Komatsu


Publisher
Elsevier Science
Year
1999
Tongue
English
Weight
148 KB
Volume
214
Category
Article
ISSN
0021-9797

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✦ Synopsis


Effects of surface-grafted polymer on the dispersibility of polymer-silica composite particles in ethyl acetate-methanol cosolvent were investigated. The composite particles were prepared by a two-step modification of monodisperse colloidal silica (120 nm in diameter). Modifications were carried out by first reacting the surface silanol of the colloidal silica with maleic anhydride-styrene copolymer silane coupling agent to prevent aggregation and then grafting, in acetone or tetrahydrofuran, amino group-terminated poly(methyl acrylate), poly(methyl methacrylate), or polystyrene to the maleic anhydride moiety on the surface. For poly-(methyl acrylate) and poly(methyl methacrylate) graftings, composite particles with long polymer chains aggregated in methanol-rich cosolvent due to insoluble secondary polymer chain interaction among the particles. Particles with a small amount of relatively low-molecular-weight secondary polymer were dispersible in the methanol content range from 0 to 90 vol%. Polystyrenemodified particles never aggregated, even in 90 vol% methanol solution. An ESR study of the suspension in ethyl acetate-hexane cosolvent suggested that the dispersibility of these composite particles in ethyl acetate-rich solution is attributable to steric repulsion between solvated and expanded secondary polymer chains among the particles. The dispersibility of the composite particles in methanol-rich solution was controlled by a delicate balance between the electrostatic repulsion and the interparticle attraction due to the desolvated and insoluble polymer chain interaction among the particles.


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