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Immersion solid solution

D In general, the formation of replaced solid solution induces the generation of defect because the lattice must be an electric charge neutral. For example, the introduction of trivalent iron ions to wiistite leads to the generation of cationic vacancy. If the other atoms are smaller, they can enter the crunode between lattice sites (called immersion solid solution). [Pg.382]

A new technique based on electrocapillary phenomena at partially immersed solid metal electrodes has been developed by Jin-Hua et al. 146,147 jhe involves the detection of the rise of a solution... [Pg.35]

To study the nature and extent of solution adsorption. A small amount of work has been done in studying the interfacial region at solid-solution interface by heat-of-immersion measurements. Few other methods show... [Pg.265]

The PEO salt complexes are generally prepared by direct interaction in solution for soluble systems or by immersion method, soaking the network cross-linked PEO in the appropriate salt solution [52-57]. Besides PEO, poly(propylene)oxide, poly(ethylene)suceinate, poly(epichlorohydrin), and polyethylene imine) have also been explored as base polymers for solid electrolytes [58]. Polyethylene imine) (PEI) is prepared by the ring-opening polymerization of 2-methyloxazoline. Solid solutions of PEI and Nal are obtained by dissolving both in acetonitrile (80 °C) followed by cooling to room temperature and solvent evaporation in vacuo. Polyethyleneimine-NaCF3S03 complexes have also been explored [59],... [Pg.104]

Some understanding of liquid flow along a solid-solution interface is useful in understanding these techniques. Consider a stationary platinum electrode immersed in a stirred solution. Three regions of solution flow can be identified. [Pg.110]

For our purposes an electrode is any solid conductor or semiconductor immersed in solution. [Pg.166]

Fig. 26. Previously synthesized homogeneous material of the quaternary X-Y-phase solid solution series (composition CuFeMo6S9), heated up to 1800 °C, and the melt regulus cooled to room temperature in less than 15 min. The figure shows relics of a darker Cu-Fe-rich sulfidic phase (approx, bornite composition) which separated from the Mo-rich sulfide. Thus, a large region of liquid immiscibility must exist throughout the quaternary system (cf. Figs. 15 and 20). Owing to some vapor loss molybdenum (white) has exsolved and remains in small droplets oriented in the sulfidic groundmass. Oil immersion, x 2500... Fig. 26. Previously synthesized homogeneous material of the quaternary X-Y-phase solid solution series (composition CuFeMo6S9), heated up to 1800 °C, and the melt regulus cooled to room temperature in less than 15 min. The figure shows relics of a darker Cu-Fe-rich sulfidic phase (approx, bornite composition) which separated from the Mo-rich sulfide. Thus, a large region of liquid immiscibility must exist throughout the quaternary system (cf. Figs. 15 and 20). Owing to some vapor loss molybdenum (white) has exsolved and remains in small droplets oriented in the sulfidic groundmass. Oil immersion, x 2500...
In conventional continuous wet finishing, a rather dilute, usually from 4 to 8% solids solution or dispersion of the chemicals Is prepared. The fabric Is then Immersed in this solution. The wet fabric Is passed through pad rollers to squeeze out the excess solution. Despite the squeezing, a cotton fabric usually retains 80 to 100% on the weight of the fabric of the finishing solution. For polyester-cotton blend fabrics, the wet pick-up Is normally 50 to 80% on the weight of the fabric. [Pg.164]

The above derivation is not restricted to just miscible solutions. It holds equally well for any other two-phase mixture, including liquid solutions in equilibrium with solid solutions, or, more importantly, to a liquid solution in equilibrium with a pure solid component (such as ice immersed in a salt solution). In that case x. = 1 refers to the pure component and we obtain... [Pg.139]

The possible constitution of the interface solid-solution of LNBr is represented by Figure 6, where a solid slide is shown emerging from a LNBr solution at a concentration lower than c s (Figure 2). On the immersed portion the negative charges of the solid may be neutralized partially by fixed cations (LN+ or H ) and partially by the ions of the Gouy layer. [Pg.240]

Unlike the systems in the PV-electrolysis category, the photoactive components in the photoelectrode based systems configuration are immersed in solution, and typically include one or more PEC solid/liquid rectifying junctions. [Pg.214]

The structural features of mixed oxides with a mosaic surface of nanoparticles, including patches of different oxide phases or a solid solution of a lower concentrated oxide in a more concentrated oxide, can strongly affect the interfacial phenomena in any media. For instance, the enthalpy of immersion in water (Table 2.1 is greater for mixed nanooxides than nanosilica. However, surface nonuniformity and the differences in the properties of a variety of surface sites result in a significant scatter in the relationship between the and 5bex values (Figure 2.1), despite a tendency of a decrease in the AH value (calculated per surface area unit) with increasing value. [Pg.341]

Solid electrolyte using polyvinylidene fluoride polymer dissolved in solvent such as dimethylacetamide, dimethylformamide, N-methyl-2-pyrrolidone, and dimethyl sulfoxide Is then cast into film. Preferred porosity of films is 70 to 80% and preferred pore diameter is 0.02 to 2 jim. Film is then immersed in solution of ethylene carbonate, propylene carbonate, or 2-methyltetrahydrofuran. [Pg.238]

Chapter 9, by Kiraly (Hungary), attempts to clarify the adsorption of surfactants at solid/solution interfaces by calorimetric methods. The author addresses questions related to the composition and structure of the adsorption layer, the mechanism of the adsorption, the kinetics, the thermodynamics driving forces, the nature of the solid surface and of the surfactant (ionic, nonionic, HLB, CMC), experimental conditions, etc. He describes the calorimetric methods used, to elucidate the description of thermodynamic properties of surfactants at the boundary of solid-liquid interfaces. Isotherm power-compensation calorimetry is an essential method for such measurements. Isoperibolic heat-flux calorimetry is described for the evaluation of adsorption kinetics, DSC is used for the evaluation of enthalpy measurements, and immersion microcalorimetry is recommended for the detection of enthalpic interaction between a bare surface and a solution. Batch sorption, titration sorption, and flow sorption microcalorimetry are also discussed. [Pg.531]

Immersion silver dissolves into the tin phase of molten solder. The silver does not melt, but rather forms a solid solution. The dissolution rate of silver is in the range of 0.5 to 1.5 jum per sec. at standard soldering temperatures. Once the silver is dissolved, the underlying copper forms intermetallics with tin as discussed previously. Flux has little effect on silver, but can help clean trace contaminates and reduce surface tension. [Pg.766]


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See also in sourсe #XX -- [ Pg.382 ]




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