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Titanium oxide preparation

The vapor-phase conversion of aniline to DPA over a soHd catalyst has been extensively studied (18,22). In general, the catalyst used is pure aluminum oxide or titanium oxide, prepared under special conditions (18). Promoters, such as copper chromite, nickel chloride, phosphoric acid, and ammonium fluoride, have also been recommended. Reaction temperatures are usually from 400 to 500°C. Coke formed on the catalyst is removed occasionally by burning. In this way, conversions of about 35% and yields of 95% have been reported. Carba2ole is frequently a by-product. [Pg.244]

Ikeue, K., Yamashita, H., and Anpo, M. (1999) Photocatalytic reduction of C02 with H20 on titanium oxides prepared within the FSM-16 mesoporous zeolite. Chemistry Letters, 28 (11), 1135—1136. [Pg.135]

Control of pore sizes of known catalysts like zeolites has been known for some time although the use of chemical vapor deposition (CVD) of organosilanes to control pore sizes has been the focus of recent research.7 Other catalysts like silica have been treated with methods like CVD and sol-gel in order to deposit thin films. Monolayer coatings of titanium oxide prepared by sol-gel methods have been recently used to coat silica and such films are active in alcohol dehydrogenation reactions.8... [Pg.9]

Most precursors used for titanium oxide preparation, especially for film production, are based on titanium alkoxides. A variety of mixed enolate-aUcoxide titanium complexes exist, such as 26a-f, 27, 28 and 29a-e, which are typical CVD precursors for titanium oxide. [Pg.977]

The samples names are referred to the template and solvent used during the preparation. Eg. Ti02-starch-cyclohexane titanium oxide prepared using soluble starch and cyclohexane as solvent. [Pg.379]

J. Li, L. Zhu, Y. Wu, Y. Harrma, A. Zhang, H. Tang, Hybrid composites of conductive polyaniline and nanocrystalline titanium oxide prepared via selfassembling and graft polymerization . Polymer, 47, 7361-7367, (2006). [Pg.176]

Titanium oxide prepared by the heat treatment of titanium sheets under nitrogen gas including a trace of oxygen had also some catalytic activity for the ORR [50]. It was fotmd that the catalytic activity for ORR on the Ti oxide catalysts increased with the increase of the specific crystalline structure, such as the Ti02 (rutile) (1 1 0) plane. XPS spectra suggested that the surface of the heat-treated titanium sheets was closed to Ti02. [Pg.404]

Vauquelin investigated cerium compounds and prepared metallic cerium, tungstates, and meteorites, which Edward Howard found to consist mainly of iron and nickel. Vauquelin showed that the minerals rutile and anatase are two varieties of titanium oxide, prepared fairly pure lead dioxide by boiling red-lead with dilute nitric acid, and determined the composition of carbon disulphide by passing the vapour over red-hot copper. ... [Pg.286]

Precipitation of a hydrated titanium oxide by mixing aqueous solutions of titanium chloride with alkaU forms the precipitation seeds, which are used to initiate precipitation in the Mecklenburg (50) variant of the sulfate process for the production of pigmentary titanium dioxide. Hydrolysis of aqueous solutions of titanium chloride is also used for the preparation of high purity (>99.999%) titanium dioxide for electroceramic appHcations (see Ceramics). In addition, hydrated titanium dioxide is used as a pure starting material for the manufacture of other titanium compounds. [Pg.120]

Alkali Metal Titanates. Alkali metatitanates may be prepared by fusion of titanium oxide with the appropriate alkah metal carbonate or hydroxide. Representative alkah metal titanates ate hsted in Table 14. The alkah metal titanates tend to be more reactive and less stable than the other titanates, eg, they dissolve relatively easily in dilute acids. [Pg.127]

Titanium oxide dichloride [13780-39-8] TiOCl2, is a yellow hygroscopic soHd that may be prepared by bubbling ozone or chlorine monoxide through titanium tetrachloride. It is insoluble in nonpolar solvents but forms a large number of adducts with oxygen donors, eg, ether. It decomposes to titanium tetrachloride and titanium dioxide at temperatures of ca 180°C (136). [Pg.131]

Veneering Investments. These are phosphate bonded and contain finely ground quart2, 2irconium oxide, and/or titanium oxide to produce highly refractory, low expansion dies of fine detail. The dies are formed within impressions taken of teeth that the dentist has prepared in anticipation of covering the front surface with an aesthetic ceramic veneer. Porcelain or ceramic powders are shaped to detail on the dies and these are fired at high (- 1000° C) temperatures to produce the veneers. The veneers are then cemented to the front surface of the previously prepared teeth. [Pg.478]

The lithium-titanium oxides are prepared by heating a mixture of anatase (Ti02) and LiOH at a high temperature. The product heated at 800-900 °C has a spinel structure of Li4/3Ti5y304. When the charge and discharge cycles are performed... [Pg.47]

Taramasso, M., Perego, G., and Notari, B. (1983) Preparation of porous crystalline synthetic material comprised of silicon and titanium oxides. US Patent 4,410,501. [Pg.234]

Recently, it is reported that Xi02 particles with metal deposition on the surface is more active than pure Ti02 for photocatalytic reactions in aqueous solution because the deposited metal provides reduction sites which in turn increase the efficiency of the transport of photogenerated electrons (e ) in the conduction band to the external sjistem, and decrease the recombination with positive hole (h ) in the balance band of Xi02, i.e., less defects acting as the recombination center[l,2,3]. Xhe catalytic converter contains precious metals, mainly platinum less than 1 wt%, partially, Pd, Re, Rh, etc. on cordierite supporter. Xhus, in this study, solutions leached out from wasted catalytic converter of automobile were used for precious metallization source of the catalyst. Xhe XiOa were prepared with two different methods i.e., hydrothermal method and a sol-gel method. Xhe prepared titanium oxide and commercial P-25 catalyst (Deagussa) were metallized with leached solution from wasted catalytic converter or pure H2PtCl6 solution for modification of photocatalysts. Xhey were characterized by UV-DRS, BEX surface area analyzer, and XRD[4]. [Pg.469]

To explore the possibility of electronic Interaction between the reduced titanium oxide and Pt, 1 ML of Pt was deposited on both fully oxidized and partially reduced T102. The reduced sample was prepared by Ar" " sputtering of the TIO2 substrate prior to metal deposition. Introducing reduced Tl centers at the Pt-Tl Interface. [Pg.84]

The Ti02 (001) surface was cleaned and reduced by cycles of ion bombardment as previously described [3]. The distribution of titanium oxidation states was determined from cxirve fitting the Ti(2p3/2) envelope in x-ray photoelectron spectra [3]. After surface preparation, reaction experiments were conducted in either the TPD or steady state mode. TPD experiments have been described [1]. XPS spectra were also obtained following a saturation exposure of the sample using the same procedure as that for the TPD experiments. After pump down, the crystal was placed under the Mg X-ray source and the Ti(2p), 0(ls), and C(ls) regions were scanned. For steady-state experiments a dosing needle was aligned perpendicular to the axis of the mass spectrometer. It was used to direct a steady beam of methylacetylene (Linde, 95%) at the crystal surface when the sample was placed at the aperture of the mass spectrometer. Steady state reaction experiments were... [Pg.298]

Heat-flow calorimetry may be used also to detect the surface modifications which occur very frequently when a freshly prepared catalyst contacts the reaction mixture. Reduction of titanium oxide at 450°C by carbon monoxide for 15 hr, for instance, enhances the catalytic activity of the solid for the oxidation of carbon monoxide at 450°C (84) and creates very active sites with respect to oxygen. The differential heats of adsorption of oxygen at 450°C on the surface of reduced titanium dioxide (anatase) have been measured with a high-temperature Calvet calorimeter (67). The results of two separate experiments on different samples are presented on Fig. 34 in order to show the reproducibility of the determination of differential heats and of the sample preparation. [Pg.257]

The sol-gel methodology can also be applied to non-hydrolytic processes. The preparation of methylsilsesqui-oxane-titanium oxide hybrid by the etherolysis-condensation of a mixture of methyltrichlorosilane and metal chloride,353 354 and by the condensation of preformed poly(methylsilsesquioxane) carrying Si-OH and Si-OCHj groups with titanium(iv) -butoxide,355 has been reported. [Pg.672]

Protection layers between the titanium metal and the electrocatalytic coating, for example, of substoichiometric titanium oxides (see Ebonex above), increase the stability by shielding the metal, for example, to avoid the formation of insulating titanium dioxide layers on the metal [35]. The preparation of such electrodes with optimal properties usually needs the special know-how of commercial suppliers. [Pg.44]

A chiral dinuclear Ti(IV) oxide 20 has been successfully designed by Maruoka and coworkers and can be used for the strong activation of aldehydes, thereby allowing a new catalytic enantioselective allylation of aldehydes with allyltributyltin (Scheme 12.18). ° The chiral catalyst 20 can be readily prepared either by treatment of bis(triisopropoxy)titanium oxide [(/-Pr0)3Ti-0-Ti(0/-Pr)3] with (S)-BINOL or by the reaction of ((5)-binaphthoxy)isopropoxytitanium chloride with silver(I) oxide. The reaction of 3-phenylpropanal with allyltributyltin (1.1 equiv) under the influence of 20 (10 mol%) gives l-phenyl-5-hexen-3-ol... [Pg.370]

U. (1978) Amorphous and crystalline titanium and iron-titanium oxides in synthetic preparations, at near ambient conditions, and in soil clays. Clays Clay Min. 26 189-201 Fitzpatrick, R.W. Naidu, R. Self, P.G. (1992)... [Pg.579]

Kormann C, Bahnemann DW, Hofmann MR (1988) Preparation and characterization of quantum-size titanium oxide J Phys Chem 92 5196-5201... [Pg.252]


See other pages where Titanium oxide preparation is mentioned: [Pg.241]    [Pg.848]    [Pg.651]    [Pg.241]    [Pg.848]    [Pg.651]    [Pg.383]    [Pg.94]    [Pg.134]    [Pg.110]    [Pg.557]    [Pg.393]    [Pg.540]    [Pg.248]    [Pg.251]    [Pg.255]    [Pg.2]    [Pg.24]    [Pg.223]    [Pg.380]    [Pg.382]    [Pg.762]    [Pg.26]    [Pg.57]    [Pg.400]    [Pg.350]   
See also in sourсe #XX -- [ Pg.266 ]




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Oxidation preparation

Oxides titanium oxide

Oxidizer preparation

Titanium oxidized

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