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Free energy coatings

Franck-Condon factors 83 Free energy, interfacial 137 Fuzzy coatings 151... [Pg.179]

The second necessary ingredient in the primitive quasichemical formulation is the excess chemical potential of the metal-water clusters and of water by itself. These quantities p Wm — can typically be obtained from widely available computational packages for molecular simulation [52], In hydration problems where electrostatic interactions dominate, dielectric models of those hydration free energies are usually satisfactory. The combination /t xWm — m//, wx is typically insensitive to computational approximations because the water molecules coat the surface of the awm complex, and computational errors can compensate between the bound and free ligands. [Pg.340]

Solute adsorption can be minimized most effectively by capillary wall coating, thereby decreasing the free energy of hydrophobic or ionic interactions. Coating can be achieved either by covalently bonded organic modifiers, e.g., polyacrylamides, sulfonic acids, polyethylene glycols, maltose, and polyvinyl pyrolidinone, or by dynamic deactivation (i.e., addition of... [Pg.29]

FIG. 13.15 Examples of the various contributions to the interaction energies between two polymer-coated particles. The curves shown illustrate qualitatively the change in Gibbs free energy due to the overlap of the tails, loops, and so on. (Redrawn with permission from Sato and Ruch 1980.)... [Pg.611]

The kinetics of the acid catalyzed hydrolysis of ethoxysilanes has been studied. Each of the silanes that were used had a phenyl or para-substituted phenyl group attached to the silicon atom. This permitted a study of the linear free energy relationships of this reaction. The reaction is of interest because of its role in silane coupling agent chemistry, in the preparation of zinc-rich silicate coatings, in the sol-gel process and in the preparation of silicones in general. [Pg.178]

Figure 13.1 Calculated energy profiles of attractive van der Waals ([cir]) and repulsive electrostatic (A) interactions between two oil droplets coated with a / -casein adsorbed layer. The diameter of each droplet was assumed to be 4 pm. The surface potential ipa for the / -casein layer was assumed to be -20 mV. The thick solid line represents the sum of attractive van der Waals and repulsive electrostatic interactions. The thick broken line represents the net free energy profile as a function of distance when steric repulsion is also taken into account. From Damodaran [293], Copyright 1997, Dekker. Figure 13.1 Calculated energy profiles of attractive van der Waals ([cir]) and repulsive electrostatic (A) interactions between two oil droplets coated with a / -casein adsorbed layer. The diameter of each droplet was assumed to be 4 pm. The surface potential ipa for the / -casein layer was assumed to be -20 mV. The thick solid line represents the sum of attractive van der Waals and repulsive electrostatic interactions. The thick broken line represents the net free energy profile as a function of distance when steric repulsion is also taken into account. From Damodaran [293], Copyright 1997, Dekker.
Petersson, A.E.V., L.M. Gustafsson, M. Nordblad, P Borjesson, B. Mattiasson and P. Adlercreutz, Wax Esters Produced by Solvent-Free Energy-Efficient Enzymatic Synthesis and Their Applicability as Wood Coatings, Green Chemistry, 7, 837-843 (2005). [Pg.75]

Rather than its being a block of uniform material, let body B be coated with a layer of material Bi of constant thickness bi. < /AmB(/) for the simplest AmB case becomes GAmBiB(7 bi). Because it is the difference in dielectric response that creates an electromagnetic interface, it is the distances between interfaces that appear in the van der Waals energy. Because there are now two spacings—Z and (Z + b )—there are two terms in the simplest-form free energy. For bj of fixed thickness and Z of variable separation, for small differences in s s, the free energy becomes (see Table P.2.b.2 in Level 2)... [Pg.65]

For measurements between crossed mica cylinders coated with phospholipid bilayers in water, see J. Marra andj. Israelachvili, "Direct measurements of forces between phosphatidylcholine and phosphatidylethanolamine bilayers in aqueous electrolyte solutions," Biochemistry, 24, 4608-18 (1985). Interpretation in terms of expressions for layered structures and the connection to direct measurements between bilayers in water is given in V. A. Parsegian, "Reconciliation of van der Waals force measurements between phosphatidylcholine bilayers in water and between bilayer-coated mica surfaces," Langmuir, 9, 3625-8 (1993). The bilayer-bilayer interactions are reported in E. A. Evans and M. Metcalfe, "Free energy potential for aggregation of giant, neutral lipid bilayer vesicles by van der Waals attraction," Biophys. J., 46, 423-6 (1984). [Pg.351]

The lower the surface free energy of the shell chemistry, the smaller is the contact angle hysteresis on the closely packed surface arrays. Further the contact angles varied with increasing height roughness. A possible explanation for this behaviour is that the vertical roughness influences the curvature radius of the liquid in trapped air pockets at the solid-liquid interface as was already assumed in the literature for nanostructured metal surfaces and paraffin-coated steel balls. [Pg.72]

The Use of Positively Charged or Low Surface Free Energy Coatings versus Polymer Brushes in Controlling Biofilm Formation... [Pg.138]


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