Adsorption of hydroxypropyl methyl cellulose in an aqueous system containing multicomponent oxide particles

Citation
Cb. Sawyer et Js. Reed, Adsorption of hydroxypropyl methyl cellulose in an aqueous system containing multicomponent oxide particles, J AM CERAM, 84(6), 2001, pp. 1241-1249
Citations number
22
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science","Material Science & Engineering
Journal title
JOURNAL OF THE AMERICAN CERAMIC SOCIETY
ISSN journal
00027820 → ACNP
Volume
84
Issue
6
Year of publication
2001
Pages
1241 - 1249
Database
ISI
SICI code
0002-7820(200106)84:6<1241:AOHMCI>2.0.ZU;2-O
Abstract
The adsorption behavior of a hydroxypropyl methyl cellulose (HPMC) polymer in aqueous suspensions of alumina, silica, kaolin, and talc powders, two-co mponent combinations, and one three-component combination was determined. P owders were well characterized by chemical analysis, XRD, DRIFT, SEM, parti cle size, surface area, and density analyses. The zeta-potential of each po wder in aqueous suspension was determined over a range of pH to determine p article charging and the isoelectric point for each material. Alumina and s ilica powders having heavily hydroxylated surfaces were observed not to ads orb the HPMC polymer over a range of pH. The Layer-type minerals talc, whic h was noticeably hydrophobic, and kaolin, which had differently hydrated ba sal planes, adsorbed the HPMC polymer but in different amounts per unit of surface area. In the two-component systems, HPMC polymer adsorption for sys tems of dispersed particles of Like electrical charge (kaolin + silica, tal c + silica or alumina, and kaolin + talc) was proportionate to the sum of t he fraction x specific surface area x adsorption capacity for each particle type. In systems where particles had an opposite electrical charge (kaolin + alumina, kaolin + talc + alumina), the HPMC polymer adsorption was signi ficantly lower than that calculated for a dispersed system. SEM analysis sh owed very fine, nonadsorbing alumina particles predominantly on the faces o f the adsorbing kaolin particles that apparently masked polymer adsorption. Results suggested a hydrophobic mechanism for the HPMC polymer adsorption and adsorption on only one face of the kaolin particles.