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Liquid-solid interactions chemical interaction

For gas-solid and liquid-solid systems, the interaction of a species with the solid surface depends on the chemical nature of the species and on the chemical and physical nature of the solid. For nonilluminated surface of semiconductor oxides, a thermodynamic equilibrium between a species and the solid is established only when the electrochemical potential of the electrons in the entire system is uniform. When the adsorption-desorption equilibrium is established, an aliquot of the species is located in an adsorbed layer, held at the surface by either weak or strong bonding forces. [Pg.8]

The liquid-solid interactions of physical (essentially van der Waals) and chemical (essentially acid-base) type can quench or put out some surface sites, so modifying their reactivity towards reagents. Therefore, in order to understand and predict the catalytic ability of given surfaces in different liquids, it is very important to measure the effective surface properties, besides the knowledge of the intrinsic properties. [Pg.544]

Fig. 3.4 Molecular dynamic simulations for the relaxation of the contact angle as a function of liquid-solid interaction (Reproduced with permission from [8], Copyright 1999 The American Chemical Society)... Fig. 3.4 Molecular dynamic simulations for the relaxation of the contact angle as a function of liquid-solid interaction (Reproduced with permission from [8], Copyright 1999 The American Chemical Society)...
This interface is critically important in many applications, as well as in biological systems. For example, the movement of pollutants tln-ough the enviromnent involves a series of chemical reactions of aqueous groundwater solutions with mineral surfaces. Although the liquid-solid interface has been studied for many years, it is only recently that the tools have been developed for interrogating this interface at the atomic level. This interface is particularly complex, as the interactions of ions dissolved in solution with a surface are affected not only by the surface structure, but also by the solution chemistry and by the effects of the electrical double layer [31]. It has been found, for example, that some surface reconstructions present in UHV persist under solution, while others do not. [Pg.314]

The new phenomenon discovered in these experiments consists in different chemical activity revealed by one and the same kind of adsorbed particles in contact with one and the same kind of molecules of the medium, but at different nature of the interface either interface of a solid (ZnO film) with a polar liquid or interface of the solid with vapours of the polar liquid. This difference is caused by the fact that in the case of contact of the film with an adsorbed layer (oxygen, alkyl radicals) with a polar liquid, the solvated ion-radicals O2 chemically interact with molecules of the solvent (see Chapter 3, Section 3.4). In the case where alkyl radicals are adsorbed on ZnO film, one can assume, by analogy with the case of adsorbed oxygen, that in the process of adsorption on ZnO, simple alkyl radicals from metalloorganic complexes of the type... [Pg.264]

Background If a nonvolatile solid is dissolved in a liquid, the vapor pressure of the liquid solvent is lowered and can be determined through the use of Raoult s Law, Pi = X 0. Raoult s Law is valid for ideal solutions wherein AH = 0 and in which there is no chemical interaction among the components of the dilute solution (see Figure 1). [Pg.261]

Chemical reactions on solid surfaces can be realized in gas-solid and liquid-solid systems. In both cases the reaction takes place on the surface of the solid matrix, and therefore the molecules to be reacted need to get in contact with the reactive surface. Several transport regimes and interaction mechanisms define the mass transfer efficiency. They can be summarized as follows [6] ... [Pg.168]

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]

Biosensor devices must operate in liquids as they measure effects at a liquid-solid interface. Then, the immobilization of the receptor molecule on the sensor surface is a key step for the efficient performance of the sensor. When the complementary analytes are flowing over the surface, they can be directly recognized by the receptor through a change in the physico-chemical properties of the sensor. In this way, the interacting components do not need to be labeled and complex samples can be analyzed without purification. [Pg.121]

Of the analytical techniques available for process analytical measmements, IR is one of the most versatile, where all physical forms of a sample may be considered - gases, liquids, solids and even mixed phase materials. A wide range of sample interfaces (sampling accessories) have been developed for infrared spectroscopy over the past 20 to 30 years and many of these can be adapted for either near-lme/at-lme production control or on-line process monitoring applications. For continuous on-line measurements applications may be limited to liquids and gases. However, for applications that have human interaction, such as near-line measurements, then all material types can be considered. For continuous measurements sample condition, as it exists within the process, may be an issue and factors such as temperature, pressure, chemical interfer-ants (such as solvents), and particulate matter may need to be addressed. In off-line applications this may be addressed by the way that the sample is handled, but for continuous on-line process applications this has to be accommodated by a sampling system. [Pg.157]

Pesticide containers were triple rinsed, crushed and disposed of as solid waste (Figure 3). Containment of liquid wastes by the newly constructed plastic lined pit was questionable after one year. There appeared to be some leakage or fluctuation of the liquid level. There is continual danger of rupture of such liners by mechanical Injury, chemical Interaction, rodents, etc., which could result in contamination... [Pg.30]

Chromatography and electrophoresis are used to separate dissolved constituents in seawater. Chromatography is based on partition of the individual components between gas or liquid passed through a column and the liquid or solid stationary phase. This partition is based on solubilities of dissolved material in the different phases and specific chemical interactions with column components. Electrophoresis separates materials on the basis of electrical charge and size as solvents flow through the plate. [Pg.73]

In order for a solid to burn it must be volatilized, because combustion is almost exclusively a gas-phase phenomenon. In the case of a polymer, this means that decomposition must occur. The decomposition begins in the solid phase and may continue in the liquid Illicit) and gas phases. Decomposition produces low molecular weight chemical compounds that eventually enter the gas phase. Heat from combustion causes further decomposition and volatilization and. therefore, further comhusiion. Thus Ihe bunting of a solid is like a chain reaction. For a compound to function as a flame retardant it must interrupt this cycle in sonic way. There are several mechanistic descriptions by which flame retardants modify flammability inen gas dilution, thermal quenching, protective coatings, physical dilution, and chemical interaction. [Pg.639]


See other pages where Liquid-solid interactions chemical interaction is mentioned: [Pg.408]    [Pg.11]    [Pg.200]    [Pg.513]    [Pg.199]    [Pg.27]    [Pg.25]    [Pg.83]    [Pg.314]    [Pg.1233]    [Pg.68]    [Pg.83]    [Pg.179]    [Pg.402]    [Pg.231]    [Pg.18]    [Pg.346]    [Pg.2]    [Pg.381]    [Pg.507]    [Pg.303]    [Pg.233]    [Pg.52]    [Pg.438]    [Pg.579]    [Pg.360]    [Pg.2]    [Pg.1]    [Pg.558]    [Pg.419]    [Pg.257]    [Pg.112]    [Pg.358]    [Pg.268]    [Pg.164]    [Pg.146]   
See also in sourсe #XX -- [ Pg.114 ]




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