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Substrate metal film

The wide range of soHd lubricants can generally be classified as either inorganic compounds or organic polymers, both commonly used in a bonded coating on a matching substrate, plus chemical conversion coatings and metal films. Since solid-film lubricants often suffer from poor wear resistance and inabihty to self-heal any breaks in the film, search continues for improved compositions. [Pg.249]

Under severe conditions and at high temperatures, noble metal films may fail by oxidation of the substrate base metal through pores in the film. Improved life may be achieved by first imposing a harder noble metal film, eg, rhodium or platinum—iridium, on the substrate metal. For maximum adhesion, the metal of the intermediate film should ahoy both with the substrate metal and the soft noble-metal lubricating film. This sometimes requires more than one intermediate layer. For example, silver does not ahoy to steel and tends to lack adhesion. A flash of hard nickel bonds weh to the steel but the nickel tends to oxidize and should be coated with rhodium before applying shver of 1—5 p.m thickness. This triplex film then provides better adhesion and gready increased corrosion protection. [Pg.251]

Figure 4.29. Sample assembly for optical shock temperature measurements. The sample consists of a metal film deposited on a transparent substrate which serves as both an anvil and a transparent window through which thermal radiation is emitted. Rapid compression of gases and surface irregularities at the interface between the sample film and the driver produce very high temperatures in this region. The bottom portion of the figure illustrates the thermal distribution across through the assembly. (After Bass et al. (1987).)... Figure 4.29. Sample assembly for optical shock temperature measurements. The sample consists of a metal film deposited on a transparent substrate which serves as both an anvil and a transparent window through which thermal radiation is emitted. Rapid compression of gases and surface irregularities at the interface between the sample film and the driver produce very high temperatures in this region. The bottom portion of the figure illustrates the thermal distribution across through the assembly. (After Bass et al. (1987).)...
The nature of the interface formed between very thin metallic films and substrates of various types has been studied extensively by AES, just as it has by XPS... [Pg.45]

The first SERS experiments were performed with electrochemically roughened electrodes and metal colloids, and many other types of suitable SERS substrates are known - e.g. metal island films, metal films over nanoparticles (see Fig. 4.58, below) or rough substrates, gratings, and sputter-deposited metal particles. [Pg.256]

C fi3 diamond films can be deposited on a wide range of substrates (metals, semi-conductors, insulators single crystals and polycrystalline solids, glassy and amorphous solids). Substrates can be abraded to facilitate nucleation of the diamond film. [Pg.16]

Friedrich et al. also used XPS to investigate the mechanisms responsible for adhesion between evaporated metal films and polymer substrates [28]. They suggested that the products formed at the metal/polymer interface were determined by redox reactions occurring between the metal and polymer. In particular, it was shown that carbonyl groups in polymers could react with chromium. Thus, a layer of chromium that was 0.4 nm in thickness decreased the carbonyl content on the surface of polyethylene terephthalate (PET) or polymethylmethacrylate (PMMA) by about 8% but decreased the carbonyl content on the surface of polycarbonate (PC) by 77%. The C(ls) and 0(ls) spectra of PC before and after evaporation of chromium onto the surface are shown in Fig. 22. Before evaporation of chromium, the C(ls) spectra consisted of two components near 284.6 eV that were assigned to carbon atoms in the benzene rings and in the methyl groups. Two additional... [Pg.273]

Bxoised area of substrate metal. In the case of passive metals defects in the passive film result in an active-passive cell with intense localised attack on the active area... [Pg.153]

The basis of Method II may be deduced from Figure 6-3. To do this, let us consider the ideal case, in which the x-rays involved are monochromatic, all influences of composition are absent, the simplest x-ray optics obtain, and excitation of a characteristic line in the film by a characteristic line of the substrate does not occur. Suppose now that a beam of intensity Iq falls upon a metal film d cm thick to excite a characteristic line of intensity Id- The contribution to Id of a volume element of constant area and of thickness dx, located at depth x, is... [Pg.154]

Figure 6. Bipolar precipitates consisting of an inner anion-selective layer and an outer cation-selective layer.19 When the electrode is polarized to the more noble side, protons and chloride ions are kept from permeating through the film, so that anodic dissolution of the substrate metal is blocked. (Reproduced from N. Sato, Corrosion, 45 354, 1989, Fig. 24 with permission of NACE International.)... Figure 6. Bipolar precipitates consisting of an inner anion-selective layer and an outer cation-selective layer.19 When the electrode is polarized to the more noble side, protons and chloride ions are kept from permeating through the film, so that anodic dissolution of the substrate metal is blocked. (Reproduced from N. Sato, Corrosion, 45 354, 1989, Fig. 24 with permission of NACE International.)...
Local breakdown of passive film results from a localized increase in the film dissolution rate at the anion adsorption sites that are attacked by chloride ions, as will be discussed later, in the same manner as substrate metal dissolution. Such acceleration of the dissolution rate was ascribed to the formation of metal chlorides24 or the local degeneration of film surface by the formation of surface electron levels.7... [Pg.236]

The surface-phase layers will difier in character depending on the stractures of metal and oxide. On certain metals (zinc, cadmium, magnesium, etc.), loose, highly porous layers are formed which can attain appreciable thicknesses. On other metals (aluminum, bismuth, titanium, etc.), compact layers with low or zero porosity are formed which are no thicker than 1 pm. In a number of cases (e.g., on iron), compact films are formed wfiicfi fiave a distorted lattice, owing to the influence of substrate metal stracture and of the effect of chemical surface forces. The physicochemical and thermodynamic parameters of such films differ from tfiose of ordinary bulk oxides. Because of the internal stresses in the distorted lattice, such films are stable only when their thickness is insignificant (e.g., up to 3 to 5 nm). [Pg.301]

LC-IR using surface-enhanced IR absorption spectroscopy (SEIRAS) was recently designed in order to develop a highly sensitive and rapid analysis method for polymer additives [506]. The method, which consists of spraying the LC eluents on to a metal film of Ag on a BaF2 substrate, allows an enhancement factor of about 90. [Pg.493]

Only two crystalline substrates have had appreciable use for the preparation of the metal film catalysts. These are mica and rocksalt. [Pg.4]


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Metals substrate

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