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Inner surface

In service inspections of French nuclear Pressure Water Reactor (PWR) vessels are carried out automatically in complete immersion from the inside by means of ultrasonic focused probes working in the pulse echo mode. Concern has been expressed about the capabilities of performing non destructive evaluation of the Outer Surface Defects (OSD), i.e. defects located in the vicinity of the outer surface of the inspected components. OSD are insonified by both a "direct" field that passes through the inner surface (water/steel) of the component containing the defect and a "secondary" field reflected from the outer surface. Consequently, the Bscan images, containing the signatures of such defects, are complicated and their interpretation is a difficult task. [Pg.171]

The physics of X-ray refraction are analogous to the well known refraction of light by optical lenses and prisms, governed by Snell s law. The special feature is the deflection at very small angles of few minutes of arc, as the refractive index of X-rays in matter is nearly one. Due to the density differences at inner surfaces most of the incident X-rays are deflected [1]. As the scattered intensity of refraction is proportional to the specific surface of a sample, a reference standard gives a quantitative measure for analytical determinations. [Pg.558]

The X-ray instrumentation requires a commercial small angle X-ray camera, a standard fine structure X-ray generator and a sample manipulator if scanning is requested. The essential signal is the relative difference between the refraction level Ir and the absorption level Ia. Both levels are measured simultaneously by two scintillation detectors. At fixed angles of deflection this signal depends solely on the inner surface density factor C and thickness d of the sample [2] ... [Pg.558]

The refractograp of figure 4 shows highly oriented micro cracks of a polystyrene sample. The orientation of the cracks is perpendicular to the mechanical strain direction. The X-ray refracted intensitiy can be interpreted as crack density, i.e. the inner surfaces within a unit volume. Changing the tilt angle (of polystyrene and polystyrene blend samples) with respect to the primary beam leads to significantly different distributions of crack orientation (Fig. 5). [Pg.560]

Ultrasonic techniques are an obvious choice for measuring the wall thickness. In the pulse-echo method times between echoes from the outer and inner surface of the tube can be measured and the wall thickness may be calculated, when the ultrasonic velocity of the material is known. In the prototype a computer should capture the measuring data as well as calculate and pre.sent the results. First some fundamental questions was considered and verified by experiments concerning ultrasonic technique (Table I), equipment, transducers and demands for guidance of the tube. [Pg.895]

One may rationalize emulsion type in terms of interfacial tensions. Bancroft [20] and later Clowes [21] proposed that the interfacial film of emulsion-stabilizing surfactant be regarded as duplex in nature, so that an inner and an outer interfacial tension could be discussed. On this basis, the type of emulsion formed (W/O vs. O/W) should be such that the inner surface is the one of higher surface tension. Thus sodium and other alkali metal soaps tend to stabilize O/W emulsions, and the explanation would be that, being more water- than oil-soluble, the film-water interfacial tension should be lower than the film-oil one. Conversely, with the relatively more oil-soluble metal soaps, the reverse should be true, and they should stabilize W/O emulsions, as in fact they do. An alternative statement, known as Bancroft s rule, is that the external phase will be that in which the emulsifying agent is the more soluble [20]. A related approach is discussed in Section XIV-5. [Pg.504]

Slurry or slip casting provides a relatively inexpensive way to fabricate unifonn-thickness, thin-wall, or large cross section shapes [4o, 44, 45, 46, 42 aiid 48]. For slip casting, a slurry is first poured into a porous mould. Capillary suction then draws the liquid from the slurry to fonn a higher solids content, close-packed, leather-hard cast on the inner surface of the mould. In a fixed time, a given wall thickness is fonned, after which the excess slurry is drained. [Pg.2766]

The net viscous force acting on this volume element is given by the difference between the frictional forces acting on the outer and inner surfaces of the shell ... [Pg.600]

Let fl C he an open, bounded and connected set with a smooth boundary T, and Tc C R be a smooth orientable two-dimensional surface. We assume that this surface can be extended up to the outer boundary T in such a way that fl is divided into two subdomains Ri, fl2 with Lipschitz boundaries. We assume that this inner surface Tc is described parametrically by the equations... [Pg.301]

The CHA is used for xps today in most commercial spectrometers. The most common version of the CHA is the 180° device shown in Figure 22. It consists of two concentric hemispherical surfaces of radii R2 and R. These surfaces have a potential difference of AH appHed between them so that the outer surface is negative and the inner surface is positive. The median equipotential surface Rq falls between these surfaces ideally, Rq = The... [Pg.284]

Articles of circular cross section may be made in iron paste molds. To keep the inner surface of the paste mold moist, it is coated with shellac or varnish and a mixture of charcoal and linseed oil is baked on. Hot iron molds ate used for ware of any shape, particularly for screw threading, multiple decoration, or raised lettering. [Pg.306]

It may be shown (33) that when the inner surface of a cylinder made of components of the same material is subjected to an internal pressure, the bote of each component experiences the same shear stress provided all components have the same diameter ratio. For these optimum conditions,... [Pg.83]

A stiU thicker coating would waste phosphor material, and by further increasing the visible reflectance of the coating would make it more difficult for visible light generated near the inner surface of the phosphor layer to get out of the lamp. [Pg.287]

The cracked products leave as overhead materials, and coke deposits form on the inner surface of the dmm. To provide continuous operation, two dmms are used while one dmm is on-stream, the one off-stream is being cleaned, steamed, water-cooled, and decoked in the same time interval. The temperature in the coke dmm is in the range of 415—450°C with pressures in the range of 103—621 kPa (15—90 psi). Overhead products go to the fractionator, where naphtha and heating oil fractions are recovered. The nonvolatile material is combined with preheated fresh feed and returned to the furnace. The coke dmm is usually on stream for about 24 hours before becoming filled with porous coke, after which the coke is removed hydraulically. [Pg.204]

Biochemically, most quaternary ammonium compounds function as receptor-specific mediators. Because of their hydrophilic nature, small molecule quaternaries caimot penetrate the alkyl region of bdayer membranes and must activate receptors located at the cell surface. Quaternary ammonium compounds also function biochemically as messengers, which are generated at the inner surface of a plasma membrane or in a cytoplasm in response to a signal. They may also be transferred through the membrane by an active transport system. [Pg.378]

A second snag test method, described by ASTM D5362, is the bean bag snag test. Each fabric specimen is made into a cover for a bean bag, which is randomly tumbled for 100 revolutions in a cylindrical test chamber fitted on its inner surface with rows of pins. Evaluation is similar to that for the mace snag test. [Pg.459]

The reduction of pH within the film unit is effected by a polymeric acid layer, as in the Polacolor process. The onset of neutralization is controlled by a contiguous timing layer. In the original SX-70 film unit these layers were on the inner surface of the transparent polyester sheet (Fig. 12) in Time-Zero SX-70 and later Polaroid integral films these layers are on the inner surface of the opaque negative support, as shown in Figure 13. [Pg.500]

FIG. 5-16 View factors for a system of two concentric coaxial c to inner cylinder, (h) Inner surface of outer cylinder to itself. [Pg.576]


See other pages where Inner surface is mentioned: [Pg.402]    [Pg.558]    [Pg.1709]    [Pg.1902]    [Pg.8]    [Pg.351]    [Pg.207]    [Pg.383]    [Pg.89]    [Pg.12]    [Pg.256]    [Pg.258]    [Pg.573]    [Pg.311]    [Pg.336]    [Pg.16]    [Pg.86]    [Pg.93]    [Pg.329]    [Pg.378]    [Pg.528]    [Pg.132]    [Pg.327]    [Pg.255]    [Pg.67]    [Pg.395]    [Pg.309]    [Pg.487]    [Pg.503]    [Pg.159]    [Pg.146]    [Pg.183]    [Pg.286]   
See also in sourсe #XX -- [ Pg.150 ]




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Adsorbent inner surface area

Apparent inner surface area of hypercrosslinked polystyrenes

Bidentate surface complexes inner-sphere

Dye molecules, zeolite L channels nanocrystals, inner- and outer-surfaces

Inner gliding surfaces

Inner surface area

Inner surface impedance

Inner surfaces, crystals

Inner, outer, and surface potentials

Inner-sphere complex surface charge

Inner-sphere mechanism surface

Inner-sphere surface complexes

Inner-sphere surface reaction

Inner-spheric surface complex

Inner-surface charge density

Ligand-exchange mechanism, inner-sphere surface complex formation

Rough Inner Surface

Supramolecularly organized luminescent dye nanocrystals, inner- and outer-surfaces

Surface Detail and Inner Granule Structure Revealed by AFM

Surface charge density inner-sphere complex

Surface-located inner coordination

Surface-located inner coordination sphere complexes

Utilization ratio of the inner surface

Vermiculite inner-sphere surface complex

Zeolite L channels, supramolecularly organized nanocrystals, inner- and outer-surfaces

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