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Oxidants mobility

A. Parihar et al., Oxidative stress and anti-oxidative mobilization in bum injury. Bums 34, 6-17 (2008)... [Pg.439]

For example, olefin sulfuri2ation products (Lubrizol, 1980), dithiophosphomolybdates (Mobil, 1980), or more simply the dithiophosphates of alcohol (Shell, 1980) whose anti-oxidant properties have been announced, are used in oil formulations for their anti-wear properties. [Pg.363]

Surface heterogeneity may be inferred from emission studies such as those studies by de Schrijver and co-workers on P and on R adsorbed on clay minerals [197,198]. In the case of adsorbed pyrene and its derivatives, there is considerable evidence for surface mobility (on clays, metal oxides, sulfides), as from the work of Thomas [199], de Mayo and co-workers [200], Singer [201] and Stahlberg et al. [202]. There has also been evidence for ground-state bimolecular association of adsorbed pyrene [66,203]. The sensitivity of pyrene to the polarity of its environment allows its use as a probe of surface polarity [204,205]. Pyrene or ofter emitters may be used as probes to study the structure of an adsorbate film, as in the case of Triton X-100 on silica [206], sodium dodecyl sulfate at the alumina surface [207] and hexadecyltrimethylammonium chloride adsorbed onto silver electrodes from water and dimethylformamide [208]. In all cases progressive structural changes were concluded to occur with increasing surfactant adsorption. [Pg.418]

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]

The use of an amperometric detector is emphasized in this experiment. Hydrodynamic voltammetry (see Chapter 11) is first performed to identify a potential for the oxidation of 4-aminophenol without an appreciable background current due to the oxidation of the mobile phase. The separation is then carried out using a Cjg column and a mobile phase of 50% v/v pH 5, 20 mM acetate buffer with 0.02 M MgCl2, and 50% v/v methanol. The analysis is easily extended to a mixture of 4-aminophenol, ascorbic acid, and catechol, and to the use of a UV detector. [Pg.613]

Acetaldehyde can be used as an oxidation-promoter in place of bromine. The absence of bromine means that titanium metallurgy is not required. Eastman Chemical Co. has used such a process, with cobalt as the only catalyst metal. In that process, acetaldehyde is converted to acetic acid at the rate of 0.55—1.1 kg/kg of terephthahc acid produced. The acetic acid is recycled as the solvent and can be isolated as a by-product. Reaction temperatures can be low, 120—140°C, and residence times tend to be high, with values of two hours or more (55). Recovery of dry terephthahc acid follows steps similar to those in the Amoco process. Eastman has abandoned this process in favor of a bromine promoter (56). Another oxidation promoter which has been used is paraldehyde (57), employed by Toray Industries. This leads to the coproduction of acetic acid. 2-Butanone has been used by Mobil Chemical Co. (58). [Pg.488]

The basic hydrolysis of tri alkyl tin haUdes and other salts forms bis(oxide)s since, except for trimethyl tin, hydroxides are unstable towards dehydration at room temperature. With tin aryl, aralkyl, and cycloalkyltin compounds, the hydroxides can be isolated. Although quite stable, they exist in mobile equiUbrium with the bisoxide and water and are easily dehydrated. Trimethyl tin hydroxide is exceptionally stable towards dehydration. [Pg.70]

At lower frequencies, orientational polarization may occur if the glass contains permanent ionic or molecular dipoles, such as H2O or an Si—OH group, that can rotate or oscillate in the presence of an appHed electric field. Another source of orientational polarization at even lower frequencies is the oscillatory movement of mobile ions such as Na". The higher the amount of alkaH oxide in the glass, the higher the dielectric constant. When the movement of mobile charge carriers is obstmcted by a barrier, the accumulation of carriers at the interface leads to interfacial polarization. Interfacial polarization can occur in phase-separated glasses if the phases have different dielectric constants. [Pg.333]

Where b is Planck s constant and m and are the effective masses of the electron and hole which may be larger or smaller than the rest mass of the electron. The effective mass reflects the strength of the interaction between the electron or hole and the periodic lattice and potentials within the crystal stmcture. In an ideal covalent semiconductor, electrons in the conduction band and holes in the valence band may be considered as quasi-free particles. The carriers have high drift mobilities in the range of 10 to 10 cm /(V-s) at room temperature. As shown in Table 4, this is the case for both metallic oxides and covalent semiconductors at room temperature. [Pg.357]

The image-related transfer of a diffusible dye formed as a product of the oxidation of a dye containing a developing agent moiety was described in 1966 (32). This process depends on the preferential transfer of an oxidation product having greater mobility than the unoxidized species. Compound [13251 -03-1] (2), for example, a bis-sulfonjlhydrazide, upon oxidation releases [573-89-7] (3), a smaller, more mobile dye. [Pg.490]


See other pages where Oxidants mobility is mentioned: [Pg.372]    [Pg.153]    [Pg.188]    [Pg.50]    [Pg.95]    [Pg.70]    [Pg.275]    [Pg.365]    [Pg.231]    [Pg.424]    [Pg.90]    [Pg.17]    [Pg.372]    [Pg.153]    [Pg.188]    [Pg.50]    [Pg.95]    [Pg.70]    [Pg.275]    [Pg.365]    [Pg.231]    [Pg.424]    [Pg.90]    [Pg.17]    [Pg.199]    [Pg.418]    [Pg.2709]    [Pg.668]    [Pg.207]    [Pg.244]    [Pg.405]    [Pg.425]    [Pg.97]    [Pg.288]    [Pg.40]    [Pg.334]    [Pg.432]    [Pg.399]    [Pg.496]    [Pg.347]    [Pg.347]    [Pg.348]    [Pg.355]    [Pg.254]    [Pg.244]    [Pg.333]    [Pg.333]    [Pg.355]    [Pg.142]    [Pg.490]    [Pg.491]    [Pg.492]   
See also in sourсe #XX -- [ Pg.46 , Pg.47 ]




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