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Oxidation initial, thin film

It is interesting to note that the most critical spectral changes occur at the initial stages of photo-oxidation. On further exposure of the samples (as a thin film on KBr) to UV light, a certain stabilization of chemical changes in the structure of the oligomers studied takes place along with a decrease in the intensity of the major absorption bands. [Pg.133]

There are also models assuming the electrostrictive input of incorporated anions into the breakdown initiation,285,299 ionic drift models,300 and many others reviewed elsewhere.283,293 However, the majority of specialists agree that further work is necessary in order to properly understand the physics of the electric breakdown in growing oxide films and that caused by electric stress in thin-film structures. [Pg.482]

Kinetic studies on the oxidations of cyclohexene, benzyl alcohol, phenol, and trans-stiVoene by [Ru (0)(tpy)(bpy(P03H2)2)] (bpy(P03H2)2) = 2,2 -bipyridine-4,4 -diphosphonic acid adsorbed to thin films of Ti02 nanoparticles on glass have been reported. There is evidence for initial two-electron steps to give Ru intermediates in all four cases. [Pg.827]

Metal oxidation is a heterogeneous solid state reaction and starts in the same way as other heterogeneous reactions with nucleation and initial growth. This was discussed in Chapter 6. A time-dependent nucleation rate may dominate the overall growth kinetics of thin Films. Even under an optical microscope (i.e., in macroscopic dimensions), preferential sites of growth can still be discerned [J. Benard (1971)). This indicates that lateral transport on the surface (e.g., at sites where screw dislocations emerge) can possibly be more important for the initial reactive growth than transport across thin oxide layers. [Pg.172]

The aminosilane coupling agent 3-aminopropyltriethoxysilane or y-amino-propyltriethoxy silane—also abbreviated as 3-APS, y-APS, APS or A1100 (Union Carbide)—is widely used to promote adhesion between polyimide thin films and mineral surfaces such as native-oxide silica, alumina and various glass ceramics [1, 2]. The structure of APS and the hydrolysis reaction sire shown in Fig. 1. Typically, dilute aqueous solutions of 0.1 vol% or approximately 0.080 wt % are employed to prime the mineral surface. The mechanism for the interaction of the bifunctional aminosilane with the mineral surface is the subject of much speculation, although it is conjectured by Linde and Gleason [3] that the amine end initially forms an electrostatic bond with surface hydroxyls. Subsequently, possibly as the result of elevated temperatures, the silanol end of the molecule proceeds to form a siloxane-like bond with the surface and the amine... [Pg.423]

Complexation studies (continued) polymer backbone, 1, 258 polymerization monitoring, 1, 259 pulse radiolysis initiation, 1, 535 in thin film and wire depositions, 1, 259 valence and oxidation number, 1, 18 t/-Complexes with niobium, 5, 66, 5, 68 with tantalum, 5, 108... [Pg.85]


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See also in sourсe #XX -- [ Pg.216 , Pg.217 ]




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Initiated oxidation

Oxidation films

Thin film oxidation

Thin oxide films

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