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Metal reversibility

Trace metals - - Reverse phase HPLC in electroplating solutions - - [313]... [Pg.151]

An example of metal dissolution via an oxidation reaction is the reaction of feiricyanide ions and copper metal. Reversing reaction (4.23) and adding to reaction (4.27) gives ... [Pg.89]

Metals Reversed-phase with tri-butylphosphate Uranium solutions AAS — 159)... [Pg.179]

Scheme 12. Oxidative-addition reactions on complexes containing the functionalized pyrazolate ligand PNNP. Depending on the electron richness of the metals, reversible or irreversible addition takes place. (Adapted from (2).]... Scheme 12. Oxidative-addition reactions on complexes containing the functionalized pyrazolate ligand PNNP. Depending on the electron richness of the metals, reversible or irreversible addition takes place. (Adapted from (2).]...
Sodium and lithium Both sodium [15] and lithium [16] electrodeposition was successful in neutral chloroaluminate ionic liquids that contained protons. These elements are interesting for Na- or Li-based secondary batteries, where the metals would serve directly as the anode material. The electrodeposition is not possible in basic or acidic chloroaluminates, only proton-rich NaQ or LiQ buffered neutral chloroaluminate liquids were feasible. The protons enlarged the electrochemical window towards the cathodic regime so that the alkali metal electrodeposition became possible. For Na the proton source was dissolved HQ that was introduced via the gas phase or via 1-ethyl-3-methylimidazolium hydrogen dichloride. Triethanolamine hydrogen dichloride was employed as the proton source for Li electrodeposition. For both alkali metals, reversible deposition and stripping were reported on tungsten and stainless steel substrates, respectively. [Pg.579]

We have been exploring new classes of molten salts or ionic liquids which possess wide electfochemical windows and are capable of electrodepositing alkali or alkali earth metals reversibly. Although the melting... [Pg.365]

Reverse osmosis is a high-pressure membrane separation process (20 to 100 bar) which can be used to reject dissolved inorganic salt or heavy metals. The concentrated waste material produced by membrane process should be recycled if possible but might require further treatment or disposal. [Pg.312]

One may rationalize emulsion type in terms of interfacial tensions. Bancroft [20] and later Clowes [21] proposed that the interfacial film of emulsion-stabilizing surfactant be regarded as duplex in nature, so that an inner and an outer interfacial tension could be discussed. On this basis, the type of emulsion formed (W/O vs. O/W) should be such that the inner surface is the one of higher surface tension. Thus sodium and other alkali metal soaps tend to stabilize O/W emulsions, and the explanation would be that, being more water- than oil-soluble, the film-water interfacial tension should be lower than the film-oil one. Conversely, with the relatively more oil-soluble metal soaps, the reverse should be true, and they should stabilize W/O emulsions, as in fact they do. An alternative statement, known as Bancroft s rule, is that the external phase will be that in which the emulsifying agent is the more soluble [20]. A related approach is discussed in Section XIV-5. [Pg.504]

Perhaps the most fascinating detail is the surface reconstruction that occurs with CO adsorption (see Refs. 311 and 312 for more general discussions of chemisorption-induced reconstructions of metal surfaces). As shown in Fig. XVI-8, for example, the Pt(lOO) bare surface reconstructs itself to a hexagonal pattern, but on CO adsorption this reconstruction is lifted [306] CO adsorption on Pd( 110) reconstructs the surface to a missing-row pattern [309]. These reconstructions are reversible and as a result, oscillatory behavior can be observed. Returning to the Pt(lOO) case, as CO is adsorbed patches of the simple 1 x 1 structure (the structure of an undistorted (100) face) form. Oxygen adsorbs on any bare 1 x 1 spots, reacts with adjacent CO to remove it as CO2, and at a certain point, the surface reverts to toe hexagonal stmcture. The presumed sequence of events is shown in Fig. XVIII-28. [Pg.737]

Markovich G, Collier C P and Heath J R 1998 Reversible metal-insulator in ordered metal nanocrystal... [Pg.2924]

As with the hydroxides, we find that whilst the carbonates of most metals are insoluble, those of alkali metals are soluble, so that they provide a good source of the carbonate ion COf in solution the alkali metal carbonates, except that of lithium, are stable to heat. Group II carbonates are generally insoluble in water and less stable to heat, losing carbon dioxide reversibly at high temperatures. [Pg.132]

Sulphur can be reduced directly to hydrogen sulphide by passing hydrogen through molten sulphur the reversible reaction H2 -I-S H2S occurs. In the laboratory the gas is most conveniently prepared by the action of an acid on a metal sulphide, iron(II) and dilute hydrochloric acid commonly being used ... [Pg.282]

The concept of the reversed fuel cell, as shown schematically, consists of two parts. One is the already discussed direct oxidation fuel cell. The other consists of an electrochemical cell consisting of a membrane electrode assembly where the anode comprises Pt/C (or related) catalysts and the cathode, various metal catalysts on carbon. The membrane used is the new proton-conducting PEM-type membrane we developed, which minimizes crossover. [Pg.220]

The commonly accepted mechanism of heterogeneously catalyzed hydrogenation involves activation of both the hydrogen and the C—C multiple bond adsorbed on the metal surface. First one hydrogen atom is transferred to the least hindered position of the multiple bond to give a half-hydrogenated adsorbed species. This reaction is fully reversible and ac-... [Pg.101]

Cyclooctatetraene can be obtained on an industrial scale by metal carbonyl catalyzed thermal tetramerization of acetylene. If cyclooctatetraene is UV-irradiated at low temperature in the presence of acetone, it is reversibly rearranged to form semibullvalene (H.E. Zimmerman, 1968, 1970). [Pg.331]

The system for shielded-metal arc welding, shown in Figure 2a, is the simplest system. It consists of the power source, electrode and holder, the base metal, and the electrical cables or leads. When the arc is stmck, a complete electrical circuit is provided. With d-c welding, the electrode maybe either negative (straight polarity) or positive (reverse polarity). Shielded metal arc welding is only used manually. [Pg.343]


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See also in sourсe #XX -- [ Pg.190 , Pg.191 ]




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Reversible metalation

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