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Ionization oxides

In both the Hquid and vapor states, phosphoms(III) oxide exists as the P40 molecule. The vapor of phosphoms(III) oxide ionizes air. Phosphoms tetroxide is made by heating P40 in a sealed tube to 440°C. P40 sublimes under vacuum at I80°C and forms colorless, glossy crystals. [Pg.373]

Unlike the cathodic reaction, anodic oxidation (ionization) of molecular hydrogen can be studied for only a few electrode materials, which include the platinum group metals, tungsten carbide, and in alkaline solutions nickel. Other metals either are not sufficiently stable in the appropriate range of potentials or prove to be inactive toward this reaction. For the materials mentioned, it can be realized only over a relatively narrow range of potentials. Adsorbed or phase oxide layers interfering with the reaction form on the surface at positive potentials. Hence, as the polarization is raised, the anodic current will first increase, then decrease (i.e., the electrode becomes passive see Fig. 16.3 in Chapter 16). In the case of nickel and tungsten... [Pg.265]

Among oxo-metals, osmium tetroxide is a particularly intriguing oxidant since it is known to oxidize various types of alkenes rapidly, but it nonetheless eschews the electron-rich aromatic hydrocarbons like benzene and naphthalene (Criegee et al., 1942 Schroder, 1980). Such selectivities do not obviously derive from differences in the donor properties of the hydrocarbons since the oxidation (ionization) potentials of arenes are actually less than those of alkenes. The similarity in the electronic interactions of arenes and alkenes towards osmium tetroxide relates to the series of electron donor-acceptor (EDA) complexes formed with both types of hydrocarbons (26). Common to both arenes and alkenes is the immediate appearance of similar colours that are diagnostic of charge-transfer absorp-... [Pg.219]

When deuterium oxide is used as D source, the reaction temperature should be considered. When water in a closed pot is heated beyond the boiling point, it becomes subcritical and, eventually, supercritical [12]. Water under these conditions should also have potential in organic reactions [13, 14]. The same should happen with deuterium oxide. The value of p K%v for subcritical water should be noted. It has the low value of ca. 11 under typical hydrothermal conditions (250°C/4—5 MPa). This means that hydrothermal deuterium oxide ionizes to a greater extent than under ambient conditions (1000 times more) and several acid-catalyzed reactions can actually be performed conveniently under supercritical or subcritical conditions without adding any acid. It is also interesting to perform transition metal-catalyzed reactions under hydrothermal conditions. Under these conditions, one should consider the redox equilibrium shown in Scheme 4 [15]. [Pg.440]

When dissolved in H2SO4 or HNO3 this oxide ionizes... [Pg.652]

Strong oxidant Ionizing radiation on dust particles... [Pg.175]

On contact with the metallic catalyst, the oxygen molecule dissociates. The atoms migrate towards the surface of the oxide support. Then, by reacting with an electron of the oxide, ionization occurs. This consumption amonnts to a modification of the oxide spaee-charge layer. [Pg.283]

Metal oxidation (ionization) at die metal-fihn interface Transport of metal cation (and/or cation vacancies) across the film Metal cation transfer into solution species (solvated, complexed) at the film-electrolyte interface. [Pg.128]

Pu (86 years) is formed from Np. Pu is separated by selective oxidation and solvent extraction. The metal is formed by reduction of PuF with calcium there are six crystal forms. Pu is used in nuclear weapons and reactors Pu is used as a nuclear power source (e.g. in space exploration). The ionizing radiation of plutonium can be a health hazard if the material is inhaled. [Pg.318]

The carriers in tire channel of an enhancement mode device exhibit unusually high mobility, particularly at low temperatures, a subject of considerable interest. The source-drain current is carried by electrons attracted to tire interface. The ionized dopant atoms, which act as fixed charges and limit tire carriers mobility, are left behind, away from tire interface. In a sense, tire source-drain current is carried by tire two-dimensional (2D) electron gas at tire Si-gate oxide interface. [Pg.2892]

Sources of Thermal Energy The most common sources of thermal energy are flames and plasmas. Flame sources use the combustion of a fuel and an oxidant such as acetylene and air, to achieve temperatures of 2000-3400 K. Plasmas, which are hot, ionized gases, provide temperatures of 6000-10,000 K. [Pg.375]

Minimizing Chemical Interferences The quantitative analysis of some elements is complicated by chemical interferences occurring during atomization. The two most common chemical interferences are the formation of nonvolatile compounds containing the analyte and ionization of the analyte. One example of a chemical interference due to the formation of nonvolatile compounds is observed when P04 or AP+ is added to solutions of Ca +. In one study, for example, adding 100 ppm AP+ to a solution of 5 ppm Ca + decreased the calcium ion s absorbance from 0.50 to 0.14, whereas adding 500 ppm POp to a similar solution of Ca + decreased the absorbance from 0.50 to 0.38. These interferences were attributed to the formation of refractory particles of Ca3(P04)2 and an Al-Ca-O oxide. [Pg.419]

These ion lasers are very inefficient, partly because energy is required first to ionize the atom and then to produce the population inversion. This inefficiency leads to a serious problem of heat dissipation, which is partly solved by using a plasma tube, in which a low-voltage high-current discharge is created in the Ar or Kr gas, made from beryllium oxide, BeO, which is an efficient heat conductor. Water cooling of the tube is also necessary. [Pg.354]

Hydrogen peroxide may react directiy or after it has first ionized or dissociated into free radicals. Often, the reaction mechanism is extremely complex and may involve catalysis or be dependent on the environment. Enhancement of the relatively mild oxidizing action of hydrogen peroxide is accompHshed in the presence of certain metal catalysts (4). The redox system Fe(II)—Fe(III) is the most widely used catalyst, which, in combination with hydrogen peroxide, is known as Fenton s reagent (5). [Pg.471]

Plasma Carburizing. Plasma carburizing generates carbon atoms at the surface by ionization of a carbon-containing gas, eg, methane. The process is similar to that described for ion nitriding. Because the process is carried out in partial vacuum, there is less chance of oxidation. [Pg.217]

Peroxophosphoric Acids and Their Salts. In its usual impure form (H PO is the main contaminant), peroxomonophosphoric acid [13598-52-2] (5), is a viscous, coloress Hquid. The three ionization constants for peroxomonophosphoric acid are pifj = 1.1, P-A2 = 5.5, and pK (peroxide proton) = 12.8 (44). Oxidations comparable to those of peroxomonosulfuric acid, H2SO, occur in acid solutions of ca pH 2, but at higher pH values, H PO becomes less reactive as an oxidant and more unstable with respect to decomposition (44). The stmcture of H PO is probably similar to that of... [Pg.93]


See other pages where Ionization oxides is mentioned: [Pg.234]    [Pg.324]    [Pg.219]    [Pg.108]    [Pg.173]    [Pg.160]    [Pg.100]    [Pg.234]    [Pg.324]    [Pg.219]    [Pg.108]    [Pg.173]    [Pg.160]    [Pg.100]    [Pg.30]    [Pg.129]    [Pg.299]    [Pg.309]    [Pg.308]    [Pg.2766]    [Pg.2809]    [Pg.46]    [Pg.107]    [Pg.314]    [Pg.6]    [Pg.41]    [Pg.382]    [Pg.25]    [Pg.6]    [Pg.157]    [Pg.137]    [Pg.431]    [Pg.435]    [Pg.228]    [Pg.343]    [Pg.361]   
See also in sourсe #XX -- [ Pg.9 , Pg.295 ]




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