Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Surface perovskites

Kirchnerova J Klvana D. Preparation and characterization of high surface perovskite electrocatalysts. Int. J. Hydrogen Energy., 1994, Volume 19, Issue 6, 501-506. [Pg.70]

Another application is in tire oxidation of vapour mixtures in a chemical vapour transport reaction, the attempt being to coat materials with a tlrin layer of solid electrolyte. For example, a gas phase mixture consisting of the iodides of zirconium and yttrium is oxidized to form a thin layer of ytnia-stabilized zirconia on the surface of an electrode such as one of the lanthanum-snontium doped transition metal perovskites Lai j.Srj.M03 7, which can transmit oxygen as ions and electrons from an isolated volume of oxygen gas. [Pg.242]

Recent applications of e-beam and HF-plasma SNMS have been published in the following areas aerosol particles [3.77], X-ray mirrors [3.78, 3.79], ceramics and hard coatings [3.80-3.84], glasses [3.85], interface reactions [3.86], ion implantations [3.87], molecular beam epitaxy (MBE) layers [3.88], multilayer systems [3.89], ohmic contacts [3.90], organic additives [3.91], perovskite-type and superconducting layers [3.92], steel [3.93, 3.94], surface deposition [3.95], sub-surface diffusion [3.96], sensors [3.97-3.99], soil [3.100], and thermal barrier coatings [3.101]. [Pg.131]

Although several metals, such as Pt and Ag, can also act as electrocatalysts for reaction (3.7) the most efficient electrocatalysts known so far are perovskites such as Lai-xSrxMn03. These materials are mixed conductors, i.e., they exhibit both anionic (O2 ) and electronic conductivity. This, in principle, can extend the electrocatalytically active zone to include not only the three-phase-boundaries but also the entire gas-exposed electrode surface. [Pg.96]

In the Lai.,CsxMn03 catalyst, the T decreases with an increase of x value and shows an almost constant value upon substitution of x>0.3. It is thought that the oxygen vacancy sites of perovskite oxide increase with an increase of amount of Cs and the oxidation activity also increases. This result is also verified by the TPR result of these catalysts(Fig. 3). As shown in Fig. 3, the reduction peak appears at low temperature with an increase of x value and no change is shown at more than x=0.3. It can thus be concluded that the catalytic performance of these oxides increases as the amount of Cs in the crystal lattice increases. However, the substitution of Cs to more than x=0.3 leads to excess Cs, which is present on the surface of mixed oxides might have no effect on the catalytic activity... [Pg.263]

Presently the effective role of sulphur additive is not well explained because sometimes activation or deactivation phenomena are observed. Such a versatile behaviour is well-illustrated over noble metal-based catalysts particularly when they are dispersed on perovskite supports [111]. The catalytic performances of a prereduced Pt/LaCo03 in H2 at 450°C are illustrated in Figure 10.13a. After preactivation in H2 subsequent bulk and surface characterisation highlighted an extensive reduction of the perovskite... [Pg.315]

Surface reconstruction has been earlier observed and reported in the literature [116]. Sequential reductive and oxidative thermal treatment usually leads to bulk transition from CoOx + La203 to LaCo03, respectively. On the other hand, the restoration of the perovskite structure is not observed under severe conditions at higher temperature. In those temperature conditions, the sintering of Co crystallites leads to irreversible redox cycle with the preferential formation of Co304 under lean conditions. [Pg.317]

The activities of the perovskite-type oxides are strongly dependent on pretreatment in reducing or oxidizing atmospheres at a.600°C. This was found for other perovskite catalysts as well (1). Reducing pretreatments lead to more active catalysts (Figures 5 and 6). The reason for this is not known, but better binding of CO to the reduced surface is a possible explanation. [Pg.264]

Paleozoic limestone (Webb et al. 2004). These kimberlites all have similar groundmass mineralogies consisting mainly of carbonate, spinel, and serpentine with lesser monticellite, mica, apatite, and perovskite (Kong et al. 1999) and they are all of volcaniclastic facies near ground surface. Varying thicknesses of clay and fine marine sediments of the Tyrell Sea ( 4000 - 12000 years BP) and 1 to 4 m of peat overlie kimberlites (Fraser et al. 2005). Bioherms composed of coral and skeletal remains of other marine organisms sometimes outcrop. [Pg.117]

Oxygen Tracer Diffusion Coefficient (D ), Oxygen Surface Exchange Coefficient (Ar) and Oxygen Ionic Conductivity (a, in air) of Doped Lanthanum Cobalt Ferrite-Based Perovskites... [Pg.151]


See other pages where Surface perovskites is mentioned: [Pg.1757]    [Pg.2205]    [Pg.2219]    [Pg.333]    [Pg.140]    [Pg.246]    [Pg.247]    [Pg.477]    [Pg.440]    [Pg.334]    [Pg.234]    [Pg.238]    [Pg.239]    [Pg.240]    [Pg.293]    [Pg.309]    [Pg.310]    [Pg.317]    [Pg.318]    [Pg.164]    [Pg.261]    [Pg.150]    [Pg.247]    [Pg.254]    [Pg.306]    [Pg.67]    [Pg.140]    [Pg.246]    [Pg.247]    [Pg.328]    [Pg.331]    [Pg.137]    [Pg.150]    [Pg.155]    [Pg.200]    [Pg.200]    [Pg.202]   
See also in sourсe #XX -- [ Pg.294 ]




SEARCH



Perovskite surfaces

© 2024 chempedia.info