Perovskite structures, high temperature

Methane or natural gas steam reforming performed on an industrial scale over nickel catalysts is described above. Nickel catalysts are also used in large scale productions for the partial oxidation and autothermal reforming of natural gas [216]. They contain between 7 and 80 wt.% nickel on various carriers such as a-alumina, magnesia, zirconia and spinels. Calcium aluminate, 10-13 wt.%, frequently serves as a binder and a combination of up to 7 wt.% potassium and up to 16 wt.% silica is added to suppress coke formation, which is a major issue for nickel catalysts under conditions of partial oxidation [216]. Novel formulations contain 10 wt.% nickel and 5 wt.% sulfur on an alumina carrier [217]. The reaction is usually performed at temperatures exceeding 700 °C. Perovskite catalysts based upon nickel and lanthanide allow high nickel dispersion, which reduces coke formation. In addition, the perovskite structure is temperature resistant. 

The ternary Ge halides, MGeX3 (M = Rb, Cs X = Cl, Br, I) are polymorphic with various distorted perovskite-like (p. 963) structures which reflect the influence of the nonbonding pair of electrons on the Ge" centre. Thus, at room temperature, rhombohedral CsGel3 has three Ge-I at 275 pm and three at 327 pm whereas in the high-temperature cubic form (above 277°C) there are six Ge-I distances at 320 pm as a result of position changes of the Ge atoms (reversible order-disorder transition). Again, RbGel3 has a lemon-yellow, orthorhombic form below —92° an intermediate, bordeaux-red orthorhombic perovskite form (—92° to —52°) a black rhombohedral form (—52° to —29°) and... 

Among the high-temperature superconductors one finds various cuprates (i.e., ternary oxides of copper and barium) having a layered structure of the perovskite type, as well as more complicated oxides on the basis of copper oxide which also include oxides of yttrium, calcium, strontium, bismuth, thallium, and/or other metals. Today, all these oxide systems are studied closely by a variety of specialists, including physicists, chemists, physical chemists, and theoreticians attempting to elucidate the essence of this phenomenon. Studies of electrochemical aspects contribute markedly to progress in HTSCs. 

It is usually difficult to discuss unambiguously on the role of the formation of sulphate, which may explain the deactivation. Their formation can equally occur on the support and on the noble metals. The poisoning effect of S02 has been reported by Qi el al. on Pd/Ti02/Al203 [112], However, in the presence of water, the stabilisation of hydroxyl groups could inhibit the adsorption of S02 [113], Burch also suggested a possible redispersion of palladium oxide promoted by the formation of hydroxyl species [114], Such tentative interpretations could correctly explain the tendencies that we observed irrespective to the nature of the supports, which indicate an improvement in the conversion of NO into N2 at high temperature. Nevertheless, the accentuation of those tendencies particularly on prereduced perovskite-based catalysts could be in connection with structural modifications associated with the reconstruction of the rhombohedral structure of... 

CUPRATE HIGH-TEMPERATURE SUPERCONDUCTORS 8.6.1 Perovskite-Related Structures and Series... 

Figure 20. Electronic structure and transport in mixed conducting perovskites. (a) Band picture of electronic structure in the high-temperature metallic phase of Lai- r tCo03-(5. (Reprinted with permission from ref 109. Copyright 1995 Elsevier.) (b) Localized picture of electron/ hole transport in semimetallic Lai- 3r Fe03-(5, involving hopping of electrons and/or electron holes (depending on the oxidation state of iron).

A natural question to ask is whether this two-regime theory is consistent with the known properties of LSM. As recently reviewed by Poulsen, the defect structure of LSM has some similarities with other more reducible perovskites such as LSG and LSF. Like these other perovskites, LSM has electrical properties on the border between that of a p-type semiconductor and a metaP and becomes oxygen substoichiometric at high temperature and low as shown in Figure 35. However, unlike its more reducible cousins (which may have significant vacancy concentration at atmospheric Pq ), LSM maintains a nearly full perovskite stoichiometry above atm and in fact becomes superstoichio-... 

La2Cu04, Sr2Cu04. As we show in chapter 6, when a perovskite forms a composite or intergrowth with other structures, new compounds of interest in catalysis can be formed (such as in high-temperature superconducting copper oxides) and EM is used to determine the structures and properties of these complex compounds. The merits of using perovskites in steam reforming, membrane catalysis and fuel cells are discussed in chapter 6. 

Chapter 10 covers the exciting field of superconductors, including high-temperature superconductors, many of which have structures related to the perovskite structure. 

---