Contact angle adsorption, effect

The adsorption isotherm corresponding to Eq. X-51 is of the shape shown in Fig. X-1, that is, it cannot explain contact angle phenomena. The ability of a liquid him to coexist with bulk liquid in a contact angle situation suggests that the him structure has been modihed by the solid and is different from that of the liquid, and in an enmirical way, this modihed structure corresponds to an effective vapor pressure F , F representing the vapor pressure that bulk liquid would have were its structure that of the... 

The first term on the right is the common inverse cube law, the second is taken to be the empirically more important form for moderate film thickness (and also conforms to the polarization model, Section XVII-7C), and the last term allows for structural perturbation in the adsorbed film relative to bulk liquid adsorbate. In effect, the vapor pressure of a thin multilayer film is taken to be P and to relax toward P as the film thickens. The equation has been useful in relating adsorption isotherms to contact angle behavior (see Section X-7). Roy and Halsey [73] have used a similar equation earlier, Halsey [74] allowed for surface heterogeneity by assuming a distribution of Uq values in Eq. XVII-79. Dubinin s equation (Eq. XVII-75) has been mentioned another variant has been used by Bonnetain and co-workers [7S]. 

The presence of pre-adsorbed polyacrylic acid significantly reduces the adsorption of sodium dodecylsulfonate on hematite from dilute acidic solutions. Nonionic polyacrylamide was found to have a much lesser effect on the adsorption of sulfonate. The isotherm for sulfonate adsorption in absence of polymer on positively charged hematite exhibits the typical three regions characteristic of physical adsorption in aqueous surfactant systems. Adsorption behavior of the sulfonate and polymer is related to electrokinetic potentials in this system. Contact angle measurements on a hematite disk in sulfonate solutions revealed that pre-adsorption of polymer resulted in reduced surface hydrophobicity. 

In the detergency process, fatty materials (i.e. dirt, often from human skin) are removed from surfaces, such as cloth fibres, and dispersed in water. It is the surfactants in a detergent which produce this effect. Adsorption of the surfactant both on the fibre (or surface) and on the grease itself increases the contact angle of the latter as illustrated in Figure 4.7. The grease or oil droplet is then easily detached by mechanical action and the surfactant adsorbed around the surface of the droplet stabilises it in solution. 

In order to achieve the above objectives, three vinyl acrylic latexes of varying butyl acrylate content have been prepared and cleaned1 for use in the study. Several anionic and nonionic surfactants commonly usod in emulsion polymerization have been used to investigate the effects of surfactant structure and polymer composition on the solubilization process. Polarity of latex surface estimated from contact angle measurements have been used to study the effect of polymer polarity on surfactant adsorption. 

To find out whether a hydrophobizing effect can be obtained by surfactant adsorption, photoresist layers processed with exposure doses between 50% and 120% of the threshold dose have been investigated by the captive bubble method. Their receding contact angle was first... 

The experiment described above does surely not yield the contact angles that determine the capillary forces since the surfactant layer is desorbed partially in water. It proves, however, that a noticeable hydrophobizing effect after surfactant adsorption can be found for the rather hydrophilic photoresist surfaces processed with the threshold dose. 

In addition to film preparation by adsorption from the melt, Compound D was also adsorbed on pure platinum surfaces by adsorption from solution in nitrobenzene, ethyl alcohol, and ethyl alcohol-water solutions. As was true of films adsorbed on chromium, adsorption on platinum from solution resulted in surface coatings exhibiting lower contact angles than those formed from the molten acid. The same postadsorption treatments were also effective in increasing the contact angles of films of Compound D on platinum. 

Figure 5. Effect of adsorbate concentration on the change in apparent critical surface tension (A) and water contact angle (B) with adsorption time for VTES films on flamed silica...

At high temperatures or in an atmosphere with a low P02, oxide films are often eliminated by dissolution in the metal, by thermodynamic decomposition or by formation of volatile sub-oxides. Even in these conditions, oxygen can still affect wettability, for instance by adsorption at metal/oxide interfaces. This effect leads to contact angles lower than the nominal contact angle of the inert system. Some examples of these oxygen effects are given in Section 6.4. Therefore, when contact... 

Liquid metals wet well metallic substrates (0 interfacial interactions unless the metallic surfaces are oxidized. Adsorption of oxygen on solid substrates can increase contact angles by tens of degrees. Intrinsic wetting seems to be slightly improved in systems with some solubility or which form intermetallics. The main effect of interfacial reactions is the disruption of oxide layers covering the metallic surfaces, allowing the formation of real metal-metal interfaces. 

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