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Titanium oxide effect

All of these results are consistent with the notion that surface migration of titanium oxide species Is an Important factor that contributes to the suppression of carbon monoxide chemisorption. The H2 chemisorption experiments on 1-2 ML of Ft, where no migration Is observed, strongly Indicate that electronic (bonding) Interactions are also occurring. Thus, for the tltanla system, both electronic Interactions and surface site blocking due to titanium oxide species must be considered In Interpreting SMSI effects. [Pg.86]

The key effect of oxide supports on the catalytic activities of metal particles is exerted through the interface between oxides and metal particles. The key objective of this study is to develop synthesis methodologies for tailoring this interface. Here, an SSG approach was introduced to modify the surface of mesoporous silica materials with ultrathin films of titanium oxide so that the uniform deposition of gold precursors on ordered mesoporous silica materials by DP could be achieved without the constraint of the low lEP of silica. The surface sol-gel process was originally developed by Kunitake and coworkers.This novel technology enables molecular-scale control of film thickness over a large 2-D substrate area and can be viewed as a solution-based... [Pg.62]

The effect of electron transfer between tungsten oxide and titanium oxide is also important in photochromatic applications. In an excellent study of aqueous sols. He et al. analyze the electronic structure of the tungsten oxide-titanium oxide system, finding that titanium oxide can catalyze the generation of W+. This state is a colored state and can be generated from WO3 WH2O by the following reactions ... [Pg.134]

In this case, titanium oxide is used both as a photocatalyst for the production of electrons and as a sink for holes, preventing recombination. This facilitates the reduction and thus the coloring of tungsten oxide. They also observe the effect of quantum confinement, resulting in band gaps in the sol that are greater than those normally observed in the bulk, as well as a blueshifted absorbance band, both results of the lack of orbital... [Pg.134]

Ranjit, K.T., Cohen, H., Willner, I., Bossmann, S., Braun, A. 1999. Lanthanide oxide-doped titanium dioxide effective photocatalysts for the degradation of organic pollutants. J Mater Sci 34 5273-5280. [Pg.158]

Fio. 22. Spectra of successive oxides of titanium, showing effect of increased oxygen on amplitude of fine structure, and showing distinction between rutile and anatase. [Pg.176]

Cai Q, Paulose M, Varghese OK, Grimes CA (2005) The effect of electrolyte composition on the fabrication of self-organized titanium oxide nanotuhe arrays hy anodic oxidation. J Mater Res 20 230-236... [Pg.355]

Titanates and silico-titanates The oxide and hydroxide of titanium are effectively used in applications of removing metal ions from water. Early studies (since 1955) have shown that hydrous titanium oxide is the most appropriate material for extracting uranium from seawater, whereas titanates and hydrous titanium oxide are suitable for removing strontium. [Pg.255]

However, unlike photosynthesis in green plants, the titanium oxide photocatalyst does not absorb visible light and, therefore, it can make use of only 3-4% of solar photons that reach the Earth. Therefore, to address such enormous tasks, photocatalytic systems which are able to operate effectively and efficiently not only under ultraviolet (UV) but also under sunlight must be established. To this end, it is vital to design and develop unique titanium oxide photocatalysts which can absorb and operate with high efficiency under solar and/or visible-light irradiation [9-16]. [Pg.284]

This chapter deals with the design and development of such unique second-generation titanium oxide photocatalysts which absorb UV-visible light and operate effectively under visible and/or solar irradiation by applying an advanced metal ion-implantation method. [Pg.284]

Figure 2 Antifogging effect of titanium oxide thin-film-coated surface. The glass mirror, whose right side was coated with titanium oxide thin film, exhibits a clear image even in a high-water-moisture room like in a batluoom. Decrease in the contact angle of a water droplet under UV irradiation of the titanium oxide thin film surface, leading to a photoin-duced superhydrophUic property of tlie minor. (Supplied by TOTO.)... Figure 2 Antifogging effect of titanium oxide thin-film-coated surface. The glass mirror, whose right side was coated with titanium oxide thin film, exhibits a clear image even in a high-water-moisture room like in a batluoom. Decrease in the contact angle of a water droplet under UV irradiation of the titanium oxide thin film surface, leading to a photoin-duced superhydrophUic property of tlie minor. (Supplied by TOTO.)...
It is important to emphasize that the photocatalytic reactivity of the metal ion-implanted titanium oxides under UV light (X < 380 nm) retained the same photocatalytic efficiency as the unimplanted original pure titanium oxides under the same UV light irradiation conditions. When metal ions were chemically doped into the titanium oxide photocatalyst, the photocatalytic efficiency decreased dramatically under UV irradiation due to the effective recombination of the photo-formed electrons and holes through the impurity energy levels formed by the doped metal ions within the band gap of the photocatalyst (in the case of Fig. 6)... [Pg.292]

Figure 10 Effect of the depth profile of V ions in the V-ion-implanted titanium oxide photocatalyst on their photocatalytic reactivity for the decomposition of NOx under visible light (X > 450 nm) irradiation at 295 K. Figure 10 Effect of the depth profile of V ions in the V-ion-implanted titanium oxide photocatalyst on their photocatalytic reactivity for the decomposition of NOx under visible light (X > 450 nm) irradiation at 295 K.
Figure 11 Effect of calcination temperature of the V-ion-implanted titanium oxide sample on the ESR spectra of + species in the V-ion-implanted titanium oxide photocatalyst at 77 K. Figure 11 Effect of calcination temperature of the V-ion-implanted titanium oxide sample on the ESR spectra of + species in the V-ion-implanted titanium oxide photocatalyst at 77 K.

See other pages where Titanium oxide effect is mentioned: [Pg.121]    [Pg.134]    [Pg.426]    [Pg.129]    [Pg.237]    [Pg.349]    [Pg.104]    [Pg.177]    [Pg.249]    [Pg.251]    [Pg.255]    [Pg.2]    [Pg.129]    [Pg.365]    [Pg.155]    [Pg.133]    [Pg.168]    [Pg.168]    [Pg.289]    [Pg.292]    [Pg.294]    [Pg.298]    [Pg.544]    [Pg.95]    [Pg.96]    [Pg.98]    [Pg.275]    [Pg.112]    [Pg.385]   
See also in sourсe #XX -- [ Pg.587 ]




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