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Interaction forces between α-alumina fibres in aqueous electrolyte measured with an atomic force microscope

The surface charging properties of polycrystalline α-alumina fibres in aqueous electrolyte solutions have been investigated by direct force and streaming potential measurements. The presence of both Al and Si on the surface of the fibres resulted in a chemically heterogeneous surface. The heterogene...

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Bibliographic Details
Published in:Colloids and surfaces. A, Physicochemical and engineering aspects Physicochemical and engineering aspects, 1999-01, Vol.146 (1), p.123-137
Main Authors: Meagher, Laurence, Franks, George V., Gee, Michelle L., Scales, Peter J.
Format: Article
Language:English
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Summary:The surface charging properties of polycrystalline α-alumina fibres in aqueous electrolyte solutions have been investigated by direct force and streaming potential measurements. The presence of both Al and Si on the surface of the fibres resulted in a chemically heterogeneous surface. The heterogeneous distribution of Si resulted in large attractive forces between the fibres at moderate to low pH values and a pzc/iep at a pH value of approximately 5.5. The origin of this force was electrostatic in nature as the force profiles were well described by the DLVO theory of colloid stability. The agreement between the direct force and streaming potential measurements was good both in terms of the magnitude of the potentials and the position of the pzc/iep. By acid washing the fibres the chemical heterogeneity of the surface was reduced and the attractive force profiles at lower pH values were not observed. Instead repulsive forces were observed which were well described by DLVO theory at all separation distances greater than 8 nm. At smaller separation distances an additional repulsive force was measured which was attributed to the presence of a Al(OH) 3 like layer on the surface of the alumina. The acid washing treatment also resulted in a shift in the pH at which the pzc/iep occurred to a value of 6.5, presumably due to a lower surface silica concentration.
ISSN:0927-7757
1873-4359
DOI:10.1016/S0927-7757(98)00779-1