Adhesion of restorative and protective materials to dentin is an important requirement for operative and preventive dentistry. Wettability and roughness are dentin substrate conditions that are critical to establishing good adhesion. This study examined superficial and deep dentin for variations in water contact angle measurements and roughness for polished, etched, dehydrated, and rehydrated states. Superficial and deep dentin disks from 6 non-carious third molars were prepared for AFM (Atomic Force Microscope) observation, roughness measurement, and contact angle measurements following specific treatments: hydrated and polished, etched (10% H3PO4), dehydrated (desiccator for 24 hrs); and rehydrated (in water for 24 hrs). Contact angles were measured by means of the ADSA (Axisymmetric Drop Shape Analysis) technique with filtered and purified water of surface tension 72.79 ergs/cm2. The AFM was used to quantify the intertubular roughness. Mean and SD of roughness and contact angle were calculated for each dentin state, and two-way Repeated Measures ANOVA with Tukey's HSD multiple comparisons were performed at p < 0.05. Wetting and roughness both increased after etching, with roughness tending to increase further while wettability dramatically decreased after desiccation. After rehydration, water contact angle values were equivalent to those of the etched condition. Although intertubular roughness did not depend on depth, lower water contact angles were found for deep dentin. Depth and dehydration resulted in altered dentin substrates with exposed hydrophobic moieties that could interfere with bonding to hydrophilic primer coats.

Individual and sequential adsorption of the anionic surfactant sodium dodecyl sulfate (SDS) and the nonionic surfactant Triton X-100 on cationic and anionic polystyrene latexes has been examined. Both latex samples, although charged differently (−16.2 and +11.0 µC cm −2 ), must be considered hydrophobic polymer colloids. The adsorbed amounts of both surfactants on cationic and anionic latexes were found to be different as a consequence of the dissimilar interfacial properties of these two surfactants. In addition, a comparison between the two surfactants showed that SDS is more easily replaced than Triton X-100 when sequential adsorption on both latexes was studied. It was found that the electrophoretic mobility of surfactant latex complexes depends on the addition sequence order of both surfactants. In relation to colloidal stability, when a layer of a nonionic surfactant is adsorbed on the surface of latexes, the electrosteric mechanism explains the experimental results. If SDS is adsorbed the stabilization or unstabilization is a consequence of the changes in the electrical repulsion between particles. However, when both surfactants are adsorbed, the assumption of additivity is not correct; that is, the electrostatic repulsion (V R ) and the steric repulsions (V osm and V vr ) are not totally independent. C 2001 Academic Press Key Words: cationic and anionic polymer colloids; nonionic and anionic surfactant adsorption; sequential adsorption; colloidal stability.

An experimental investigation of the electrokinetic phenomena known as primary electroviscous effect with suspensions of polystyrene spheres is described. A characteristic coefficient of the effect has been measured by an automatic method for the determination of the viscosity of liquids through capillary viscometers. In order to compare this coefficient with the values predicted by different theoretical models, the electrophoretic mobility of the spheres was measured by means of a microelectrophoresis apparatus. The zeta potential was calculated from the results with a complete theory of the electrophoresis of spherical particles. The comparison between theoretical and experimental values of the electroviscous effect shows that the theories of Booth and of Watterson and White reproduce very well the general trend of the experimental results, althogh they seem to underestimate the latter.

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