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Perovskites conductivity

A large deposit of perovskite was found recently in the USA (Powderhom). Perovskite deposits are also known to be found in Russia (Cola Pennisula). There is little information available on research into flotation of perovskite conducted on ores from some Russian deposits [6], These ores are relatively complex and contain a variety of gangue minerals including pyroxene, amphibole, olivine, nepheline, biotite and calcite. [Pg.182]

Besides the glass seal interfaces, interactions have also been reported at the interfaces of the metallic interconnect with electrical contact layers, which are inserted between the cathode and the interconnect to minimize interfacial electrical resistance and facilitate stack assembly. For example, perovskites that are typically used for cathodes and considered as potential contact materials have been reported to react with interconnect alloys. Reaction between manganites- and chromia-forming alloys lead to formation of a manganese-containing spinel interlayer that appears to help minimize the contact ASR [219,220], Sr in the perovskite conductive oxides can react with the chromia scale on alloys to form SrCr04 [219,221],... [Pg.198]

Calcination. Calcination involves a low (<1000° C) temperature soHd-state chemical reaction of the raw materials to form the desired final composition and stmcture such as perovskite for BaTiO and PZT. It can be carried out by placing the mixed powders in cmcibles in a batch or continuous kiln. A rotary kiln also can be used for this purpose to process continuously. A sufficiendy uniform temperature has to be provided for the mixed oxides, because the thermal conductivity of powdered materials is always low. [Pg.205]

At the other end of the conduction spectrum, many oxides have conductivities dominated by electron and positive hole contributions to the extent that some, such as Re03, SnOa and tire perovskite LaCrOs have conductivities at the level of metallic conduction. High levels of p-type semiconduction are found in some transition metal perovskites especially those containing alio-valent ions. Thus the lanthairum-based perovskites containing transition metal ions, e.g. LaMOs (M-Cr, Mn, Fe, Co, Ni) have eirlranced p-type semiconduction due to the dependence of the transition metal ion valencies on the ambient... [Pg.161]

Good results are obtained with oxide-coated valve metals as anode materials. These electrically conducting ceramic coatings of p-conducting spinel-ferrite (e.g., cobalt, nickel and lithium ferrites) have very low consumption rates. Lithium ferrite has proved particularly effective because it possesses excellent adhesion on titanium and niobium [26]. In addition, doping the perovskite structure with monovalent lithium ions provides good electrical conductivity for anodic reactions. Anodes produced in this way are distributed under the trade name Lida [27]. The consumption rate in seawater is given as 10 g A ar and in fresh water is... [Pg.216]

However, in the case of the perovskite even the application of sintering temperatures as high as 1200 °C did not result in a higher overall ionic conductivity. Since the total ionic conductivity is two orders of magnitude lower than the bulk conductivity in polycrystalline Li0 34La05] Ti 0294, an improvement by way of the preparation route is necessary rather than changes in the lattice by the addition of dopants,... [Pg.538]

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]

Fig. 2 shows the temperature as a function of irradiation time of Cu based material under microwave irradiation. CuO reached 792 K, whereas La2Cu04, CuTa20e and Cu-MOR gave only 325, 299 and 312 K, respectively. The performances of the perovskite type oxides were not very significant compared to the expectation from the paper reported by Will et al. [5]. This is probably because we used a single mode microwave oven whereas Will et al. employed multi-mode one. The multi-mode microwave oven is sometimes not very sensitive to sample s physical properties, such as electronic conductivity, crystal sizes. From the results by electric fixmace heating in Fig. 1, at least 400 K is necessary for NH3 removal. So, CuO was employed in the further experiments although other materials still reserve the possibility as active catalysts when we employ a multi-mode microwave oven. [Pg.311]

Double Substitution In such processes, two substitutions take place simultaneously. For example, in perovskite oxides, La may be replaced by Sr at the same time as Co is replaced by Fe to give solid solutions Lai Sr Coi yFey03 5. These materials exhibit mixed ionic and electronic conduction at high temperatures and have been used in a number of applications, including solid oxide fuel cells and oxygen separation. [Pg.425]

Another important group of oxide materials with a very low electrical conductivity is the oxide dielectrics. A number of these are based upon the perovskites, MXO3 or M0 X02. The archetype of these materials is BaTiC>3, which has a high dielectric constant, or relative permittivity to vacuum, the value at room temperature being 1600, and commercial use is made of the isostructural PbTi(>3 and ZrTi03 which form solid solutions, the PZT dielectrics. These materials lose their dielectric properties as the temperature... [Pg.159]

Oxides play many roles in modem electronic technology from insulators which can be used as capacitors, such as the perovskite BaTiOs, to the superconductors, of which the prototype was also a perovskite, Lao.sSro CutT A, where the value of x is a function of the temperature cycle and oxygen pressure which were used in the preparation of the material. Clearly the chemical difference between these two materials is that the capacitor production does not require oxygen partial pressure control as is the case in the superconductor. Intermediate between these extremes of electrical conduction are many semiconducting materials which are used as magnetic ferrites or fuel cell electrodes. The electrical properties of the semiconductors depend on the presence of transition metal ions which can be in two valence states, and the conduction mechanism involves the transfer of electrons or positive holes from one ion to another of the same species. The production problem associated with this behaviour arises from the fact that the relative concentration of each valence state depends on both the temperature and the oxygen partial pressure of the atmosphere. [Pg.236]

The superconducting oxides include both perovskites and Ruddlesden-Popper compounds which have an orthorhombic arrangement of cubic cells, alternatively of the perovskite and sodium chloride structures. The common feature of all of these is the presence of copper as a major component. The first ceramic superconductor was a lanthanum-strontium substituted cuprate (Lai Sr Cu04 z), which is a perovskite, but subsequently the inter-oxide compound Y203 2BaO 3CuO, commonly referred to as a 123 compound, was shown to have superior performance. The speculation concerning the conduction mechanism is that this involves either Cu3+-Cu2+ positive hole... [Pg.247]


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See also in sourсe #XX -- [ Pg.170 ]




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Conductivities in perovskites

Conductivity electric, perovskite-type oxides

Conductivity sensors perovskite materials

Defect Chemistry in Proton-Conducting Perovskites

Double perovskite conductivity

Electrical conductivity perovskites

Electronic conductivity metallic perovskites

Electronic conductivity perovskite band structure

Electronic conductivity perovskite superconductors

Intermediate-Temperature SOFCs Using Proton-Conducting Perovskite

Ionic Conduction in Perovskite-Type Compounds

Lithium Conduction in the Perovskite Structure

Mechanisms of Proton Conduction (Undoped, Cubic Perovskites)

Mechanisms of Proton Conduction in Perovskite-Type Oxides

Mixed protonic-electronic conducting perovskite membrane

Mixed-conducting perovskite membranes

Mixed-conducting perovskite reactor

Mixed-conducting perovskite reactor for high-temperature applications

Oxide Ion Conductivity in Perovskite Oxides

Oxide Ion Conductivity in the Perovskite-Related Oxides

Perovskite anion conductivity

Perovskite electronic conductivity

Perovskite metallic conductivity

Perovskite oxides conductivity

Perovskite oxides proton conductivity

Perovskite proton conduction

Perovskite proton conductivities

Perovskite proton-conducting ceramic membrane

Perovskite protonic-electronic conductivity

Perovskite-type materials proton conducting ceramics

Perovskite-type mixed-conducting

Perovskite-type mixed-conducting materials

Perovskites lithium conduction

Perovskites proton conductivity

Proton Conduction in Cerium- and Zirconium-Based Perovskite Oxides

Proton Conductivity in Acceptor-Doped Simple Perovskites, ABO

Proton Conductivity in Perovskite Oxides

Proton-conducting perovskites

Requirements for Oxygen Anion and Electronic Conduction within Perovskites

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