Layered Rutiles

By using an exfoliation and flocculation technique, Prasad et al. were able to prepare a polyaniline/NbWOe hybrid material [74]. Dispersed nanosheets of HNbWOe were obtained by treating HNbWOe with tetrabutyl ammonium hydroxide. The suspension of the exfoliated layers was then added to an alcoholic solution of aniline, followed by addition of a few drops of 1M HCl, and overnight sonication in order to induce flocculation of the aniline-NbWOe nanocomposite. The nanocomposite was isolated by centrifugation, and dried. Treatment of the nanocomposite with O2 at 130 °C for several weeks resulted in the formation of intercalated PANI. 

The polymerization of aniline in the galleries of layered HNbMoOe was also reported by Byeon et al. Anihne was first inserted into the structure via an acid-base reaction to produce (anihnium)xNbMo06, which upon treatment with FeCl3 as an oxidizing agent resulted in the formation of (PANl)xNbMo06 [76]. 

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The experimental material was a sample of rutile on which a layer of tnicrocrystalline titania had been deposited. Isotherms of nitrogen were determined on the original material outgassed at 1S0°C and on samples that had been outgassed at 25°, 150° or 250°C respectively after being charged with n-nonane. 

Langmuir-Blodgett films (LB) and self assembled monolayers (SAM) deposited on metal surfaces have been studied by SERS spectroscopy in several investigations. For example, mono- and bilayers of phospholipids and cholesterol deposited on a rutile prism with a silver coating have been analyzed in contact with water. The study showed that in these models of biological membranes the second layer modified the fluidity of the first monolayer, and revealed the conformation of the polar head close to the silver [4.300]. 

In203 has the C-type M2O3 structure (p. 1238) and InO(OH) (prepared hydrothermal ly from In(OH)3 at 250-400°C and 100-1500 atm) has a deformed rutile structure (p. 961) rather than the layer lattice structure of AIO(OH) and GaO(OH). Crystalline In(OH)3 is best prepared by addition of NH3 to aqueous InCl3 at 100° and ageing the precipitate for a few hours at this temperature it has the simple Re03-type structure distorted somewhat by multiple H bonds. 

After gas-phase oxidation reaction finished, the reactor wall surfece was coated with a thick rough scale layer. The thickness of scale layer along axial direction was varied. The scale layer at front reactor was much thicker than that at rear. The SEM pictures were shown in Fig. 1 were scale layers stripped from the reactor wall surface. Fig. 1(a) was a cross sectional profile of scale layer collected from major scaling zone. Seen from right side of scale layer, particles-packed was loose and this side was attached to the wall surface. Its positive face was shown in Fig. 1(b). Seen from left side of scale layer, compact particles-sintered was tight and this side was faced to the reacting gases. Its local amplified top face was shown in Fig. 1(c). The XRD patterns were shown in Fig. 2(a) were the two sides of scale layer. Almost entire particles on sintered layer were characterized to be rutile phase. While, the particle packed layer was anatase phase. 

Besides, without addictive AICI3 as a crystal conversion agent, phase composition of most neogenic Ti02 particles was anatase in our experiment. Conversions active energy finm anatase to rutile was 460 kJ/mol [5], with temperature arose, crystal conversion rate as well as mass fraction of rutile would increase [6,7]. Hence, after a lot of heat accumulated, phase composition of particle-sintered layer was rutile. 

Baudoin etal. [168,169] first presented qualitative depth profiles of lacquer and polymer coatings by means of r.f. GD-OES. Quantitative depth profiles were successively obtained by Payling et al. [170] on prepainted metal coated steel. Samples comprised a (rutile) pigmented silicone-modified polyester topcoat over a polymer primer, on top of an aluminium-zinc-silicon alloy coated steel substrate. With GD-OES in r.f. mode, it was possible to determine the depth profile through the polymer topcoat, polymer primer coat, metal alloy coating, and alloy layer binding to the steel substrate with a total depth of 50 im, all in about 60 min on the one sample. GD-OES depth profiles of unexposed and weathered silicone-modified polyesters were also reported [171]. Radiofrequency GD-OES has further been used to... 

Uniformity of the electrical double layer on oxides plot of -gj vs -ApH master curves for rutile, ruthenium dioxide and hematite. The concentration of KNO3 is indicated. 

Temperature congruence for the double layer on rutile in the presence of the indicated concentrations of KN03. Between 5 and 50° C all data coincide within the band width. 

Figure 3.16 The pair potential for rutile in ethylene glycol at infinite dilution as a function of diffuse layer potential. Background concentration 1 x 10 4 Ml ] electrolyte...

The mechanism of interaction of amino acids at solid/ aqueous solution interfaces has been investigated through adsorption and electrokinetic measurements. Isotherms for the adsorption of glutamic acid, proline and lysine from aqueous solutions at the surface of rutile are quite different from those on hydroxyapatite. To delineate the role of the electrical double layer in adsorption behavior, electrophoretic mobilities were measured as a function of pH and amino acid concentrations. Mechanisms for interaction of these surfactants with rutile and hydroxyapatite are proposed, taking into consideration the structure of the amino acid ions, solution chemistry and the electrical aspects of adsorption. 

Fokkink, L.G. de Keizer, J. Lyklema, J. (1989) Temperature dependence of the electrical double layer on oxides. Rutile and hematite. 

Polycrystalline oxide materials, both undoped and doped, have been extensively examined for use as photoanodes. Ti02 electrodes have been prepared by thermal oxidation of a Ti plate in an electric furnace in air at 300-800°C (15-60 min) and in a flame at 1300°C (20 min) [27-30]. XRD analysis of thermally oxidized samples indicates the formation of metallic sub-oxide interstitial compounds, i.e. TiOo+x (x < 0.33) or Ti20i y (0 < y < 0.33) and Ti30 together with rutile Ti02 [27]. The characteristic reflection of metallic titanium decreases in intensity after prolonged oxidation (60 min) at 800° C indicating the presence of a fairly thick oxide layer (10-15 pm). Oxidation at 900°C leads to poor adhesion of the oxide film... 

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