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Normal titania

The usual catalysts in SCR processes consist of mixed transition metal oxides. Normally titania is taken as support, among the additional compounds WO3, M0O3 and especially V2O5 seem to be the most frequently used [2]. The nature of the active vanadia species and its interaction with the underlying titania have been discussed controversially. However, there is now general agreement that thin layers of vanadium oxide on anatase are required as active and selective catalysts in several important industrial processes [3-7]. [Pg.547]

Minerals. Iron-bearing minerals are numerous and are present in most soils and rocks. However only a few minerals are important sources of iron and thus called ores. Table 2 shows the principle iron-bearing minerals. Hematite is the most plentiful iron mineral mined, followed by magnetite, goethite, siderite, ilmenite, and pyrite. Siderite is unimportant in the United States, but is an important source of iron in Europe. Tlmenite is normally mined for titania with iron as a by-product. Pyrite is roasted to recover sulfur in the form of sulfur dioxide, leaving iron oxide as a by-product. [Pg.413]

Figure 16.6 TEM micrographs of titania-supported Au particles. The nominal thickness of An was (a) 0.13 nm (h) 0.78nm (c) 1.56nm (d) 2.33 nm. The Au deposition rate was 2.6 X 10 nms. Particle size distributions of Au for various deposition times are shown in the plot, with the distrihutions fitted to a normal Gaussian function. Figure 16.6 TEM micrographs of titania-supported Au particles. The nominal thickness of An was (a) 0.13 nm (h) 0.78nm (c) 1.56nm (d) 2.33 nm. The Au deposition rate was 2.6 X 10 nms. Particle size distributions of Au for various deposition times are shown in the plot, with the distrihutions fitted to a normal Gaussian function.
Preparation of chiral mesoporous materials has become a great interest for material scientists. Normally chiral property is introduced into chiral mesoporous material via an organic chiral templating component. But, by using a sonochemical method, Gabashvili et al. [36] have prepared mesoporous chiral titania using a chiral inorganic precursor and a non-chiral dodecylamine as a template. Size of the pores was 5.5 nm. [Pg.201]

Figure 12.1 Generation of photocatalytic active species at the surface of titania particles (NHE = normal hydrogen electrode). Figure 12.1 Generation of photocatalytic active species at the surface of titania particles (NHE = normal hydrogen electrode).
The solid-state Si SPE NMR spectra of SBA-15 and the titania surface-coated SBA-15 (Ti-SBA-15) are in accord with this expectation. The spectrum of SBA-15 displays a broad as)mimetric peak at 109 ppm (Q" sites) with shoulders at —101 ppm (Q sites) and 90 ppm(Q sites) in the area ratio 79 19 2. The NMR spectrum of Ti-SBA-15 (one layer) shows a reduction of the band intensity relative to the intensity. The normalized Q Q Q site populations become 85 13 2. No asymmetry is observed in the Q site band. Repetition of the monolayer deposition to form a double layer of titania on silica yields a material whose Si NMR spectrum is indistinguishable from that of the Ti-SBA-15 with a monolayer coverage. As expected, the titania-insulated silica resonances are unperturbed by the second titania layer. [Pg.64]

Titania is being examined for use as a base material for bonded stationary phases because of its stability and its ability to separate bases under normal-phase conditions.Other researchers are investigating silica that has been surface modified with titanium oxide followed by the immobilization of poly(methyloctylsiloxane). These columns show promise for routine chromatographic analyses, but more research needs to be performed to evaluate the best manufacturing methods. [Pg.615]

In ophthalmic glass production, the cerium-titania complex is combined with manganese to produce the pink U. V. absorptive tinted glasses. The manganese which normally gives a purple color is toned down with the yellow color giving a yellowish pink. In addition, the cerium absorption in the U. V. is an important property of the glass. [Pg.85]

Burch and Flambard (113) have recently studied the H2 chemisorption capacities and CO/H2 activities of Ni on titania catalysts. They attributed the enhancement of the catalytic activities for the CO/H2 reaction (after activation in H2 at 450°C) to an interfacial metal-support interaction (IFMSI). This interaction is between large particles of Ni and reduced titanium ions the Ti3+ is promoted by hydrogen spillover from Ni to the support, as pictured in Fig. 8. The IFMSI state differs from the SMSI state since hydrogen still chemisorbs in a normal way however, if the activation temperature is raised to 650°C, both the CO/H2 activity and the hydrogen chemisorption are suppressed. They define this condition as a total SMSI state. Between the temperature limits, they assumed a progressive transition from IFMSI to SMSI. Such an intermediate continuous sequence had been... [Pg.22]

Many metal oxides have been made in the form of nanotubes, but most of them have an amorphous wall. SEM is normally used to characterize these materials. For some crystalline oxide nanotubes, HRTEM is the only technique to determine their structures. Titania-related nanotubular material is a good example. [Pg.479]

Due to its high photocatalytic activity towards the complete mineralisation of VOCs [7,8] titania in its anatase form is normally used. Using ceramic monoliths with high titania content (50%) the total oxidation of chlorinated organic compounds at low temperature has been demonstrated [9]. However, since the photons from natural light may only penetrate a few microns into the catalyst surface the use of a wash-coating technique, where only a thin active film of titania is applied to the ceramic or metallic support can be considered as an ideal technique to produce maintenance free photocatalytic reactors. [Pg.737]

Commercial SCR catalyst used in connection with coal-based power stations are generally composed of base metals, since platinum-group metal catalysts are too readily poisoned and have too narrow an operating temperature window for this application. Favored compositions are titania-based together with active components, normally oxides of vanadium, tungsten, or molybdenum. For these systems the optimum reaction temperature is usually in the range 3(XM00°C. [Pg.86]

The titania used for catalysis is commonly prepared by the aqueous hydrolysis of titanium salts or by the flame hydrolysis of TiCl4. 48 jt jg found in two crystalline forms, rutile and anatase, with the form produced depending on the temperature and preparation procedure used. Anatase is more stable at the temperatures normally used for catalytic processes and, thus, is the more common support. The anatase prepared by flame hydrolysis of TiCl4 has surface areas near 40-80 m2/g and mean pore diameters of about 50 nm. That prepared by aqueous... [Pg.165]

Hydrothermal conditions are frequently used to synthesize (e g., Yang et al. 2000 Wang and Ying 1999 Yanagisawa and Ovenstone 1999) and treat (Penn and Banfield 1998, 1999a,b) nanocrystalline titania samples. The surrounding phase now is water or an aqueous solution. Experiments are normally conducted between 100-300° C and at relatively low pressures (at 300°C the saturated vapor pressure of water is only 8.5 MPa (CPC book), far less than pressures applied in many solid state phase transformation experiments). [Pg.32]

K. K. Native and modified alumina, titania and zirkonia in normal and reversed-phase high-performance liquid chromatography, Chromatographia, 1996, 42, 217-222. [Pg.427]

The restauration of a normal state by exposure to oxygen is explained by the reoxydation of the support with the filling of surface anionic vacancies (Eqv6) which increases titania s work function and requires the retrocession of excess electrons to the oxide. [Pg.203]


See other pages where Normal titania is mentioned: [Pg.203]    [Pg.203]    [Pg.134]    [Pg.578]    [Pg.120]    [Pg.281]    [Pg.26]    [Pg.373]    [Pg.255]    [Pg.221]    [Pg.25]    [Pg.82]    [Pg.157]    [Pg.257]    [Pg.552]    [Pg.5]    [Pg.120]    [Pg.134]    [Pg.169]    [Pg.453]    [Pg.19]    [Pg.45]    [Pg.5918]    [Pg.5923]    [Pg.435]    [Pg.507]    [Pg.452]    [Pg.1050]    [Pg.1745]    [Pg.30]    [Pg.275]    [Pg.5]    [Pg.30]    [Pg.91]    [Pg.92]    [Pg.204]   
See also in sourсe #XX -- [ Pg.65 , Pg.66 ]




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