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Metal oxides ionic

In view of the above-said it is necessary to investigate oxide solubilities in the melts based on alkali-metal halides and to establish regularities in metal-oxide-ionic melt systems . Such data are required for predicting the stability of melts doped with additions of metal cations, and of electrochemical cells containing chlorides of transition metals, under the action of oxide ions formed in the melt owing to oxidation or pyrohydrolysis of its constituent parts. [Pg.265]

V.L. Cherginets, T.G. Deineka, O.V. Demirskaya, T.P. Rebrova, Estimation of interface energy of metal oxide/ionic melt system from data on lead oxide solubility in molten KCl-NaCl eutectic, Prepr., Chemistry Preprint Server, http //preprint.chemweb.com/ physchem/0103006 Uploaded 2 March 2001, p. 3. [Pg.369]

At present, various oxygen sensors using metal oxide ionic conductors or oxide saniconductors are available for a wide variety of applications. It was shown that fluoride ion conductors such as LaFj, PbFj (Yamazoe and Miura 1990), and PbSnF (Kuwato et al. 1990,1997 Wakagi and Kuwano 1994) can also be used for these purposes. Table 6.5 summarizes solid-state oxygen sensors based on fluoride... [Pg.214]

The result is the formation of a dense and uniform metal oxide layer in which the deposition rate is controlled by the diffusion rate of ionic species and the concentration of electronic charge carriers. This procedure is used to fabricate the thin layer of soHd electrolyte (yttria-stabilized 2irconia) and the interconnection (Mg-doped lanthanum chromite). [Pg.581]

With decreasing amounts of metal oxide, the degree of polymerisation increases. Chains of linked tetrahedra form, like the long chain polymers with a -C-C- backbone, except that here the backbone is an -Si-O-Si-O-Si- chain (Fig. 16.4c). Two oxygens of each tetrahedron are shared (there are two bridging oxygens). The others form ionic bonds between chains, joined by the MO. These are weaker than the -Si-O-Si- bonds which form the backbone, so these silicates are fibrous asbestos, for instance, has this structure. [Pg.171]

A number of olefins may be polymerised using certain metal oxides supported on the surface of an inert solid particle. The mechanism of these polymerisation reactions is little understood but is believed to be ionic in nature. [Pg.37]

Addition of metallic oxides to isobutene polymerized by high energy radiation leads to a spectacular increase in the yield.313. It seems that some ions are stabilized by complexing with the surface of the oxide and such an interaction prevents their recombination with the gegen-ions. These observations confirm therefore the suggested cause of inefficient ionic polymerization in systems exposed to ionizing radiation. [Pg.157]

The magnetic criterion is particularly valuable because it provides a basis for differentiating sharply between essentially ionic and essentially electron-pair bonds Experimental data have as yet been obtained for only a few of the interesting compounds, but these indicate that oxides and fluorides of most metals are ionic. Electron-pair bonds are formed by most of the transition elements with sulfur, selenium, tellurium, phosphorus, arsenic and antimony, as in the sulfide minerals (pyrite, molybdenite, skutterudite, etc.). The halogens other than fluorine form electron-pair bonds with metals of the palladium and platinum groups and sometimes, but not always, with iron-group metals. [Pg.313]

Seven chemical reactions were identified from the chemistry syllabus. These chemical reactions were selected because they were frequently encountered during the 2-year chemistiy course and based on their importance in understanding concepts associated with three topics, namely, acids, bases and salts, metal reactivity series and inorganic chemistry qualitative analysis. The seven types of chemical reactions were combustion of reactive metals in air, chemical reactions between dilute acids and reactive metals, neutralisation reactions between strong acids and strong alkalis, neutralisation reactions between dilute acids and metal oxides, chemical reactions between dilute acids and metal carbonates, ionic precipitation reactions and metal ion displacement reactions. Although two of the chemical reactions involved oxidation and reduction, it was decided not to include the concept of redox in this study as students had only recently been introduced to ion-electron... [Pg.155]

Third, students understanding of the triplet relationship for a particular type of reaction may be further consolidated by carrying out additional similar reactions using different reactants (e.g., using several metal oxides to react with different dilute acids will help illustrate the similarities in the chemical reactions although different salts are produced). Once students become aware of the similarities in the chemical reactions, they would be more likely to meaningfully deduce the ionic equations for the chemical reactions instead of the common practice of cancelhng out the spectator ions from the overall balanced chemical equation. [Pg.166]

Based on the concept of mixed-framework lattices, we have reported a novel class of hybrid solids that were discovered via salt-inclusion synthesis [4—7]. These new compounds exhibit composite frameworks of covalent and ionic lattices made of transition-metal oxides and alkali and alkaline-earth metal halides, respectively [4]. It has been demonstrated that the covalent frameworks can be tailored by changing the size and concentration of the incorporated salt. The interaction at the interface of these two chemically dissimilar lattices varies depending upon the relative strength of covalent vs. ionic interaction of the corresponding components. In some cases, the weak interaction facilitates an easy... [Pg.239]

A special class of ionically conducting melts are the oxide-based systems (usually, mixtures of a metal oxide and a nomnetal oxide, e.g., CaO and Si02) with melting points between 1200 and 2500°C. Such melts are often formed in the high-temperature processes of metallurgy. [Pg.131]

Metal oxides of variable oxidation state as supports or support modifiers [202] are well known in gold catalysis. In the previous section we have already indicated some metal-support interactions influencing the electronic state of gold nanoparticles as well as the metallic or ionic state of gold. Of the numerous literatures we have to mention Haruta and Date [169], Bond [195], as well as Goodman works [186,203]. Further results can be found on the iron oxide system in recent literatures [162,204]. [Pg.100]


See other pages where Metal oxides ionic is mentioned: [Pg.165]    [Pg.166]    [Pg.165]    [Pg.166]    [Pg.24]    [Pg.275]    [Pg.425]    [Pg.591]    [Pg.2219]    [Pg.2398]    [Pg.285]    [Pg.91]    [Pg.522]    [Pg.52]    [Pg.494]    [Pg.495]    [Pg.175]    [Pg.140]    [Pg.442]    [Pg.111]    [Pg.129]    [Pg.255]    [Pg.736]    [Pg.19]    [Pg.165]    [Pg.55]    [Pg.247]    [Pg.353]    [Pg.334]    [Pg.24]    [Pg.428]    [Pg.431]    [Pg.99]    [Pg.545]    [Pg.382]    [Pg.248]    [Pg.102]    [Pg.122]   
See also in sourсe #XX -- [ Pg.666 ]

See also in sourсe #XX -- [ Pg.686 ]




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Oxides ionic

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