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Surface penetration

SIMS Secondary Ion mass spectroscopy A beam of low-energy Ions Impinges on a surface, penetrates the sample and loses energy In a series of Inelastic collisions with the target atoms leading to emission of secondary Ions. Surface composition, reaction mechanism, depth profiles... [Pg.1852]

Figure 8. Structure of the corrosion layer at the grid surface. Penetration and corrosion rates are approximated for room temperature and normal float voltage (2.23-2.25 V/cell) (see text). Figure 8. Structure of the corrosion layer at the grid surface. Penetration and corrosion rates are approximated for room temperature and normal float voltage (2.23-2.25 V/cell) (see text).
Hardness is determined by hardness tests which involve the measurement of a material s resistance to surface penetration by an indentor with a force applied to it The indentation process occurs by plastic deformation of metals and alloys. Hardness is therefore inherently related to plastic flow resistance of these materials. Brittle materials, such as glass and ceramics at room temperature, can also be subjected to hardness testing by indentation. This implies that these materials are capable of plastic flow, at least at the microscopic level. However, hardness testing of brittle materials is frequently accompanied by unicrack formation, and this fact makes the relationship between hardness and flow strength less direct than it is for metals. [Pg.28]

A distinction has been drawn (1) between harvest and ultimate residues. The former term is being defined as the surface or penetrated residue of insecticide at the time of harvest, whereas the latter designation refers to the residues in or on the foodstuff, whether fresh or processed, at the time of consumption. Thus, there exist harvest surface and penetration or harvest total residues, as well as ultimate surface, penetration, and total residues. Where necessary, component parts of the foodstuff may be specified to delimit this concept further. [Pg.137]

When a surfactant is injected into the liquid beneath an insoluble monolayer, surfactant molecules may adsorb at the surface, penetrating between the monolayer molecules. However it is difficult to determine the extent of this penetration. In principle, equilibrium penetration is described by the Gibbs equation, but the practical application of this equation is complicated by the need to evaluate the dependence of the activity of monolayer substance on surface pressure. There have been several approaches to this problem. In this paper, previously published surface pressure-area Isotherms for cholesterol monolayers on solutions of hexadecy1-trimethyl-ammonium bromide have been analysed by three different methods and the results compared. For this system there is no significant difference between the adsorption calculated by the equation of Pethica and that from the procedure of Alexander and Barnes, but analysis by the method of Motomura, et al. gives results which differ considerably. These differences indicate that an independent experimental measurement of the adsorption should be capable of discriminating between the Motomura method and the other two. [Pg.133]

Figure 9.8 Isolated-boundary (Type-B) self-diffusion associated with a stationary grain boundary, (a) Grain boundary of width 6 extending downward from the free surface at y = 0. The surface feeds tracer atoms into the grain boundary and maintains the diffusant concentration at the grain boundary s intersection with the surface at the value cB(y = 0, t) = 1. Diffusant penetrates the boundary along y and simultaneously diffuses transversely into the grain interiors along x. (b) Diffusant distribution as a function of scaled transverse distance, xi, from the boundary at scaled depth, yx, from the surface. Penetration distance in grains is assumed large relative to 5. Figure 9.8 Isolated-boundary (Type-B) self-diffusion associated with a stationary grain boundary, (a) Grain boundary of width 6 extending downward from the free surface at y = 0. The surface feeds tracer atoms into the grain boundary and maintains the diffusant concentration at the grain boundary s intersection with the surface at the value cB(y = 0, t) = 1. Diffusant penetrates the boundary along y and simultaneously diffuses transversely into the grain interiors along x. (b) Diffusant distribution as a function of scaled transverse distance, xi, from the boundary at scaled depth, yx, from the surface. Penetration distance in grains is assumed large relative to 5.
Equation (6.1.6) gives the rate of displacement of the crack tip under the stress and chemical reaction, and can also be used to calculate the static fatigue limit. If we assume after Wiederhorn (1968) that the rate of displacement of the crack tip is roughly equal to the rate of surface penetration, then... [Pg.260]

Since the strain arising from an ideal sharp indenter cannot be wholly elastic (as is the case with a blunt indenter), a number of new specific features of failure of a particular material may arise, especially in the early stages of crack formation under the influence of surface penetration at low loads. It is reasonable to suppose at the same time that as the crack region extends widely below the contact zone, the influence of indenter geometry should become significant. [Pg.266]

For A n = 0.2-50eV, surface penetration into the first monolayers reduces the temperature for epitaxy and yields a higher density of structures. These processes dominate in sputtering and PLD at higher background pressures of 0.05-0.5mbar. [Pg.309]

After about two days, see Figures 4 and 5a, crystallization is observed at the surface of the gel spheres. Pyramids of which the basal plane coincides with the sphere surface penetrate into the sphere body. Despite the supersaturation of the silica source no abundant nucleation is observed on the sphere surface. According to XRD and FTIR measurements the pyramids consist of ZSM-5 framework with TPA as guest molecules. [Pg.264]

Equation 9.4 provides a relationship between time and the distance at which a particular concentration is achieved. When clearance rates are small relative to diffusion rateS/ it states that the distance from the surface (penetration depth) at which a particular concentration C is achieved advances as the square root of time. In other wordS/ to double the penetration of a compound/ the exposure time must quadruple. Equation 9.5 states that/ given sufficient time and negligible plasma concentration/ most compounds will develop a semilogarithmic concentration profile whose slope is determined by the ratio of the clearance rate to the diffusion constant. Note also that the distance over which the concentration decreases to... [Pg.109]

Two basic types of finishes (or treatments) are used to protect wood surfaces during outdoor weathering those that form a film, layer, or coating on the wood surface, and those that penetrate the wood surface to leave no distinct layer or coating. Film-forming materials include paints of all description, varnishes, lacquers, and also overlays bonded to the wood surface. Penetrating finishes include preservatives, water repellents, pigmented semitransparent stains, and chemical treatments. [Pg.437]

The photovoltages of 0.50 to 0.75 V obtained in the present work are fairly larger than those obtained in aqueous solutions ( 0.5 V) [2-4]. This may be due to a decrease in surface carrier recombination centers (such as surface penetrated H atoms) in p-Si by a decrease in the H concentration in solution, or due to a beneficial effect of TEA cations on the CO2 reduction reported in the literature [7-9]. Further studies are now in progress. [Pg.568]

The next step in the entry process is endocytic uptake of the bound toxin. The uptake is comparatively slow and appears to occur from clathrin-coated pits (Morris ef al., 1985). Once in endosomes, the toxin is exposed to acidic conditions a pH below 5.3 is necessary for the penetration to the cytosol (Sandvig and Olsnes, 1981). If acidification of the endosomes is prevented by exposure of the cells to NH4CI or monensin, the cells are protected from poisoning. However, the protection can be overcome if the cells are exposed to buffer with acidic pH (Sandvig and Olsnes, 1981). Under these conditions toxin bound at the cell surface penetrates directly through the surface membrane (Moskaug etal., 1988). [Pg.276]

Isothermal (593 to 693 K) ar-time curves for the decomposition of lanthanum oxalate [81] were sigmoid but asymmetrical with the decay period being the more pronounced. The Prout-Tompkins equation applied in two linear regions with , = 132 kJ mol. A branching chain mechanism was proposed during which channels fi om the surface penetrate the crystals as reaction proceeds. The predominant initial product was carbon monoxide, which disproportionated to yield carbon dioxide, and the residual solid contained carbonate and finely divided carbon. [Pg.460]


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See also in sourсe #XX -- [ Pg.287 ]




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