Controlled structure copolymers for the dispersion of highperformance ceramics in aqueous media

Citation
M. Vamvakaki et al., Controlled structure copolymers for the dispersion of highperformance ceramics in aqueous media, J MAT CHEM, 11(10), 2001, pp. 2437-2444
Citations number
37
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science","Material Science & Engineering
Journal title
JOURNAL OF MATERIALS CHEMISTRY
ISSN journal
09599428 → ACNP
Volume
11
Issue
10
Year of publication
2001
Pages
2437 - 2444
Database
ISI
SICI code
0959-9428(2001)11:10<2437:CSCFTD>2.0.ZU;2-Z
Abstract
Statistical copolymers of a methoxy oligo( ethylene glycol) methacrylate (O EGMA) and either 2-(dimethylamino) ethyl methacrylate (DMA) or methacrylic acid (MAA) have been examined as dispersants for barium titanate powder in water and water-isopropyl alcohol mixtures. The dispersing efficiency of th e polymers was assessed using gravitational sedimentation and by measuring the particle size distributions of the dispersed powders by disk centrifuge photosedimentometry (DCP). OEGMA copolymers with MAA were very efficient, causing the mean particle size of the dispersed powder to decrease by an or der of magnitude in the presence of dispersant. In contrast, OEGMA-DMA copo lymers were completely ineffective. The best MAA copolymers gave higher dis persion efficiency over a wider pH range (pH 1 to 10) compared to a typical commercial dispersant Darvan-C, which was efficient only above pH 7. X-Ray photoelectron spectroscopy, zeta potential measurements, infra red sp ectroscopy and DCP studies all show that the acid-containing copolymers bin d strongly to the barium titanate surface via the carboxylic acid groups re sulting in good quality dispersions. There were no changes in the dispersio n quality due to desorption of the dispersant even after extensive washing and drying of the copolymer-coated particles. The dried particles showed co mplete redispersion in water even after washing and drying, again indicatin g strong binding of the copolymer to the oxide surface.