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Interactions between solid surfaces and

Addition of free water in the reaction mixture may also affect positively. However, the addition of free water cannot always be appropriate, since without sufficient chemical interaction with the substrate oxide it would not work or even can be harmful reducing the main effect of mechanical loading. Chemical interaction between solid surfaces and water under mechanical activation significantly differs from static conditions. During comminution, solids are subjected to dynamic loading that results in the extension and compression of chemical bonds. This process is believed to be similar to corrosion under pressure [29]. [Pg.3]

The problem of the nature and the extent of a relationship between catalytic activity and position in the periodic table is important not only in the formulation of a general theory of catalysis but also in respect to the more fundamental problem of interaction between solid surfaces and surrounding phases. There is definite evidence on the important role of unfilled d-bands of transition metals for low-temperature chemisorption of hydrogen ). [Pg.716]

Interactions between solid surfaces and solutions are of fundamental importance in many biological systems (joint lubrication and movement, implant rejection, etc.), as well as in mechanics (lubrication and adhesion), in agriculture (soil wetting and conditioning and pesticide application), in communica-... [Pg.199]

Another system of great interest relates to the interactions between solid surfaces and dilute polymer solutions. Frequently the solids in question are in the form of colloids, presenting areas of the order of 50 to 300 m% to the exterior solution phase. The polymer chains may be bondable to the solid surfaces at one end, both ends, and/or along the chain, depending on the chemistry. [Pg.646]

The intention of the present chapter was to present mostly the prospective advantages, but also some limitations, of the use of isothermal calorimetry at the Solid-Liquid interface as a powerful tool in the study of interactions between solid surfaces and... [Pg.263]

The question of the conditions to be satisfied by a moving fluid in contact with a solid body was one of considerable difficulty for quite some time, as pointed out by Goldstein (1965), and the assumption of no-slip is now generally accepted for practical purposes. On the other hand, if we can make an artificial solid surface where there is very little interaction between the surface and the liquid in contact with it, slip would be appreciable for liquid flow. The analysis of the phenomenon was presented by Watanabe et al. (1999). [Pg.135]

The authors applied this model to the situation of dissolving and deposited interfaces, involving chemically interacting species, and included rate kinetics to model mass transfer as a result of chemical reactions [60]. The use of a stochastic weighting function, based on solutions of differential equations for particle motion, may be a useful method to model stochastic processes at solid-liquid interfaces, especially where chemical interactions between the surface and the liquid are involved. [Pg.80]

The structure, the thickness, and the interactions generated by the presence of the adsorbed polymer layers have been extensively studied [17], In particular, the force between two polymer-covered mica sheets in various solvency conditions has been probed via the SEA technique [27,28], The force is purely repulsive in a good solvent and becomes attractive as the solvent gets poorer. However, these studies concern only a regime of large interaction compared to the thermal energy and are restricted to interactions between solid surfaces. [Pg.64]

The competition between molecular-based and molecule-substrate interactions is one of the features that make supramolecular assemblies based on the combination of molecular components and solid substrates so exciting and also potentially useful from the applications point of view. The control issue is whether can one achieve long-lived charge separation between molecular components when immobilized on a surface, and from the fundamental perspective, can the interactions between the surface and molecular components be manipulated In this section, the immobilization of molecular components consisting of at least two electroactive and/or photoactive units will be discussed. The intramolecular interactions within these dyads in solution, as well as their behavior as interfacial supramolecular triads when immobilized on nanocrystalline TiC>2, will be compared. [Pg.289]

Electrostatic interactions occur between the ionic head groups of the surfactant and the oppositely charged solid surface (head down adsorption with monolayer structure) [56]. Acid-base interactions occur due to hydrogen bonding or Lewis acid-Lewis base reactions between solid surface and surfactant molecules (head down with monolayer structure) [57]. Polarisation of jt electrons occurs between the surfactant head group which has electron-rich aromatic nuclei and the positively charged solid surface (head down with monolayer structure) [58]. Dispersion forces occur due to London-van der Waals forces between the surfactant molecules and the solid surface (hydrophobic tail lies flat on the hydrophobic solid surface while hydrophilic head orients towards polar liquid) [59]. [Pg.40]

An empirical method to estimate the surface tension of a solid is Zisman s plot (cos 9 as a function of yl), which obtains the critical surface tension of wetting. In the absence of specific interaction between the surface and the liquids used for the measurement of contact angles, the critical contact angle of wetting can be accurately estimated and its value used as the surface tension of the surface. However, if a surface interacts with liquids used as the sessile droplet for the contact angle measurement, to the extent that the surface tension is altered, Zisman s plots deviate from the ideal linear relationship. In a strict sense, the plot is applicable only to imperturbable surfaces with which liquid contact does not alter surface configuration, i.e., no surface dynamics applies. [Pg.514]

The literature was reviewed to describe the newest efforts to synthesize and characterize supported polynuclear metal complexes as adsorbents and catalysts. This review includes our attempts to model the equilibrium structures and properties of the metal complexes, using simple quantum mechanics, as a means to understand better the interactions between the surface and the metal complexes. Special attention is directed towards the characterization of the supported metal complexes before and after ligand removal. We compare these modeling results with observations in the literature so as to understand better the fundamental processes that govern the interactions between the metal complexes and the surfaces. With this enhanced understanding of these governing factors, it should be easier to prepare oxide solids decorated with metal complexes having the desired physico-chemical properties. [Pg.72]

The interaction between silica surface and nitrogen compounds was studied by using mainly solid state NMR. The quinoline as basic nitrogen compound and carbazole as non-basic nitrogen compound were adsorbed on the dry or wet silica. Both of them made a hydrogen bonded hydroxyl proton on the surface of silica. Surface water on the silica might effect on the interaction between silica surface and nitrogen compounds. [Pg.584]

Van Loosdrecht et al. (1990) have investigated systematically the adhesion of microorganisms to solid surfaces in aquatic environments and describe the initial adhesion process in terms of a colloid-chemical theory. These workers focus on the interplay of (1) electrostatic interactions between bacterial surfaces and solid surfaces and (2) on the hydrophobic and steric energies of these surfaces. Adsorbed polymers can influence bacteria-surface interactions in several ways (1) electrostatic repulsions, (2) steric hinderance caused by mono-... [Pg.856]

Because catalysis is concerned primarily with the surfaces of solids, some attention should be given to any specialized defects associated with the surface of a solid, and to the possible interaction between the surface and defects in the bulk. We note first that the surface itself is a defect, since the interface between a regular lattice of interacting particles and a vacuum must be the seat of either unusual atom spacings or stresses, and of either free valences or special terminating groups. This itself determines or affects some properties of catalytic importance, and likewise has a bearing on the nature of surface defects and of their formation by radiation. [Pg.121]

The interactions between solid particles and surfaces can fall into a number of different categories of forces ... [Pg.45]

The behavior of protein molecules at solid surfaces is very complex. The interaction between the surface and the protein is determined both by the nature of the protein, the surface and the medium outside the surface. The situation is further complicated by the fact that exchange reactions between protein molecules of the same or different kinds take place on the surface. Except for these exchange reactions most protein molecules appear to be irreversibly adsorbed. Although the details of the interaction between protein molecules and surfaces are not known it is assumed that general properties of the surface and the protein such as hydrophobicity, charge density, ion binding, hydration etc. are involved. For reviews, see e.g (21.35-37). [Pg.482]

In this short review, we have presented some results on the behavior of polymer solutions close to surfaces in the context of adhesion phenomena. The emphasis has been placed on the interaction between two flat parallel solid surfaces induced by a polymer solution and more specifically on the bridging effect between the surfaces due to the polymer. Two types of interactions between the surface and the polymer have been considered grafting and adsorption. [Pg.161]

Oscillatory structural forces appear in thin films of pure solvent between two smooth solid surfaces and in thin liquid films containing colloidal particles including macromolecules and surfactant micelles (Israelachvili 1992). In the first case, the oscillatory forces are called the solvation forces and they are important for the short-range interactions between solid particles and dispersions. In the second case, the structural forces affect the stability of foam and emulsion films as well as the flocculation processes in various colloids. At lower particle concentrations, the structural forces degenerate into the so-called depletion attraction, which is found to destabilize various dispersions. [Pg.17]

The following approach, originally described by Derjaguin et al. [21], lays out the path to the experimental determination of the free energy of interaction between solid surfaces. A comparison of the values of the free energy of interaction per unit area, Aafh), between flat-parallel surfaces and the force p(h) between two spherical particles of radius R of the same solid phase in the same medium separated by the same distance h, indicates that the two values are proportional to each other, namely. [Pg.28]

Below, we begin with a brief description of the numerical SCF model. In prior studies, we used this method to determine the free energies as a function of surface separation for polymer-coated surfaces in solution. Here, we describe our findings for die interactions between solid surfaces immersed in (1) a singlecomponent melt and (2) a melt that contains polymers with surface-active end-groups We also introduce an analytical SCF model for the melt containing end-functionalized chains and present the results from this theory. Comparisons are made between the numerical and analytical SCF results and die implications of these findings are discussed furdier in the Conclusions section. [Pg.370]


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