Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Thickness layer

The layer thickness affects the ease in achieving the desired degree of compaction. In general, the thicker the layer, the easier it is to achieve the desired compaction, since it retains its heat for a longer period (lower rate of heat loss). [Pg.419]

Layers with a thickness between 25 and 40 mm, if possible, should not be laid during cold winter months, or greater attention should be given to the duration of compaction, which should be as short as possible. [Pg.419]

More information about this subject can be found in Brown (1980), Daines (1985) and Nicholls et al. (2008). [Pg.419]


For detection of defect dimensions defectometers were used made of examined sample material allowing to reveal defects of 0.25-1% x-rayed steel layer thickness in range of 100-500mm thickness at 11 MeV. [Pg.514]

Steel was used as the control object. During the experiments radiation energy, steel layer thickness, focal distance, roentgen films, screens were varied. Sensitivity was valued according to wire and groove standards. [Pg.514]

General hydrodynamic theory for liquid penetrant testing (PT) has been worked out in [1], Basic principles of the theory were described in details in [2,3], This theory enables, for example, to calculate the minimum crack s width that can be detected by prescribed product family (penetrant, excess penetrant remover and developer), when dry powder is used as the developer. One needs for that such characteristics as surface tension of penetrant a and some characteristics of developer s layer, thickness h, effective radius of pores and porosity TI. One more characteristic is the residual depth of defect s filling with penetrant before the application of a developer. The methods for experimental determination of these characteristics were worked out in [4]. [Pg.613]

One can see from the formulas (1) and (2) that PT sensitivity strongly depends on the thickness of a developer s layer. But during liquid s penetration into developer s layer the powder particles are sinking and more tightly packing each other. It results in decrease of layer thickness h Physical meaning of the influence of this process upon defect s detection is obvious as follows. [Pg.614]

One more obvious example illustrates strong influence of particle s sedimentation upon the sensitivity threshold. Assume that we have to ensure the detection of the cracks with the depth 10 > 2 mm in the case when the same product family indicated above is applied and h = 20 pm. The calculation using formula (1) shows that in the absence of sedimentation only the cracks with the width H > 2 pm could be detected. But when the effect of sedimentation results in the reduction of the value of developer layer thickness from h = 20 pm to h = 8 pm, then the cracks of substantially smaller width H > 0,17 pm can be revealed at the same length lo = 2 mm. Therefore we can state that due to the sedimentation of developer s particles the sensitivity threshold has changed being 12 times smaller. Similar results were obtained using formula (2) for larger particles of the developers such as kaolin powder. [Pg.615]

Other SFA studies complicate the picture. Chan and Horn [107] and Horn and Israelachvili [108] could explain anomalous viscosities in thin layers if the first layer or two of molecules were immobile and the remaining intervening liquid were of normal viscosity. Other inteipretations are possible and the hydrodynamics not clear, since as Granick points out [109] the measurements average over a wide range of surface separations, thus confusing the definition of a layer thickness. McKenna and co-workers [110] point out that compliance effects can introduce serious corrections in constrained geometry systems. [Pg.246]

The polymer concentration profile has been measured by small-angle neutron scattering from polymers adsorbed onto colloidal particles [70,71] or porous media [72] and from flat surfaces with neutron reflectivity [73] and optical reflectometry [74]. The fraction of segments bound to the solid surface is nicely revealed in NMR studies [75], infrared spectroscopy [76], and electron spin resonance [77]. An example of the concentration profile obtained by inverting neutron scattering measurements appears in Fig. XI-7, showing a typical surface volume fraction of 0.25 and layer thickness of 10-15 nm. The profile decays rapidly and monotonically but does not exhibit power-law scaling [70]. [Pg.402]

This intensity can be used to calculate the correlation fiinction (Bl.9.101) and the interface distribution fiinction (B 1.9.102) and to yield the lamellar crystal and amorphous layer thicknesses along the fibre. [Pg.1408]

The preparation of the reflecting silver layers for MBI deserves special attention, since it affects the optical properties of the mirrors. Another important issue is the optical phase change [ ] at the mica/silver interface, which is responsible for a wavelength-dependent shift of all FECOs. The phase change is a fimction of silver layer thickness, T, especially for T < 40 mn [54]. The roughness of the silver layers can also have an effect on the resolution of the distance measurement [59, 60]. [Pg.1735]

O, a large current is detected, which decays steadily with time. The change in potential from will initiate the very rapid reduction of all the oxidized species at the electrode surface and consequently of all the electroactive species diffrising to the surface. It is effectively an instruction to the electrode to instantaneously change the concentration of O at its surface from the bulk value to zero. The chemical change will lead to concentration gradients, which will decrease with time, ultimately to zero, as the diffrision-layer thickness increases. At time t = 0, on the other hand, dc-Jdx) r. will tend to infinity. The linearity of a plot of i versus r... [Pg.1929]

Figure B3.6.3. Sketch of the coarse-grained description of a binary blend in contact with a wall, (a) Composition profile at the wall, (b) Effective interaction g(l) between the interface and the wall. The different potentials correspond to complete wettmg, a first-order wetting transition and the non-wet state (from above to below). In case of a second-order transition there is no double-well structure close to the transition, but g(l) exhibits a single minimum which moves to larger distances as the wetting transition temperature is approached from below, (c) Temperature dependence of the thickness / of the enriclnnent layer at the wall. The jump of the layer thickness indicates a first-order wetting transition. In the case of a conthuious transition the layer thickness would diverge continuously upon approaching from below. Figure B3.6.3. Sketch of the coarse-grained description of a binary blend in contact with a wall, (a) Composition profile at the wall, (b) Effective interaction g(l) between the interface and the wall. The different potentials correspond to complete wettmg, a first-order wetting transition and the non-wet state (from above to below). In case of a second-order transition there is no double-well structure close to the transition, but g(l) exhibits a single minimum which moves to larger distances as the wetting transition temperature is approached from below, (c) Temperature dependence of the thickness / of the enriclnnent layer at the wall. The jump of the layer thickness indicates a first-order wetting transition. In the case of a conthuious transition the layer thickness would diverge continuously upon approaching from below.
The most significant commercial product is barium titanate, BaTiO, used to produce the ceramic capacitors found in almost all electronic products. As electronic circuitry has been rniniaturized, demand has increased for capacitors that can store a high amount of charge in a relatively small volume. This demand led to the development of highly efficient multilayer ceramic capacitors. In these devices, several layers of ceramic, from 25—50 ]lni in thickness, are separated by even thinner layers of electrode metal. Each layer must be dense, free of pin-holes and flaws, and ideally consist of several uniform grains of fired ceramic. Manufacturers are trying to reduce the layer thickness to 10—12 ]lni. Conventionally prepared ceramic powders cannot meet the rigorous demands of these appHcations, therefore an emphasis has been placed on production of advanced powders by hydrothermal synthesis and other methods. [Pg.500]

To yield high storage densities, layer thicknesses in the order of the focused laser beam are necessary in the storage medium, measuring about 1 )Tm. In commercial WORM disks based on pure dye layers, layer thicknesses are even lower at about 0.1 )Tm. With thicknesses as low as these, it becomes... [Pg.140]

Aluminum, the most common material used for contacts, is easy to use, has low resistivity, and reduces surface Si02 to form interfacial metal-oxide bonds that promote adhesion to the substrate. However, as designs reach submicrometer dimensions, aluminum, Al, has been found to be a poor choice for metallization of contacts and via holes. Al has relatively poor step coverage, which is nonuniform layer thickness when deposited over right-angled geometric features. This leads to keyhole void formation when spaces between features are smaller than 0.7 p.m. New collimated sputtering techniques can extend the lower limit of Al use to 0.5-p.m appHcations. [Pg.348]

An even wider range of wavelength, toward the infrared, can be covered with quantum well lasers. In the Al Ga As system, compressively strained wells of Ga In As are used. This ternary system is indicated in Figure 6 by the line joining GaAs and In As. In most cases the A1 fraction is quite small, X < 0.2. Such wells are under compressive strain and their thickness must be carefully controlled in order not to exceed the critical layer thickness. Lasers prepared in this way are characterized by unusually low threshold current density, as low as ca 50 A/cm (l )-... [Pg.131]


See other pages where Thickness layer is mentioned: [Pg.171]    [Pg.85]    [Pg.286]    [Pg.615]    [Pg.174]    [Pg.186]    [Pg.190]    [Pg.242]    [Pg.403]    [Pg.403]    [Pg.1934]    [Pg.1934]    [Pg.2677]    [Pg.2752]    [Pg.2989]    [Pg.2]    [Pg.105]    [Pg.431]    [Pg.585]    [Pg.148]    [Pg.150]    [Pg.173]    [Pg.173]    [Pg.175]    [Pg.179]    [Pg.181]    [Pg.184]    [Pg.185]    [Pg.185]    [Pg.192]    [Pg.122]    [Pg.133]    [Pg.133]    [Pg.134]   
See also in sourсe #XX -- [ Pg.143 ]

See also in sourсe #XX -- [ Pg.322 ]

See also in sourсe #XX -- [ Pg.139 ]

See also in sourсe #XX -- [ Pg.102 ]

See also in sourсe #XX -- [ Pg.212 , Pg.215 , Pg.306 ]

See also in sourсe #XX -- [ Pg.421 ]

See also in sourсe #XX -- [ Pg.21 ]

See also in sourсe #XX -- [ Pg.226 , Pg.227 , Pg.228 ]

See also in sourсe #XX -- [ Pg.62 ]

See also in sourсe #XX -- [ Pg.72 ]

See also in sourсe #XX -- [ Pg.71 , Pg.143 , Pg.145 , Pg.154 , Pg.170 ]

See also in sourсe #XX -- [ Pg.72 ]

See also in sourсe #XX -- [ Pg.586 ]

See also in sourсe #XX -- [ Pg.572 , Pg.574 , Pg.600 , Pg.603 ]

See also in sourсe #XX -- [ Pg.226 ]




SEARCH



Absorber layer thickness

Active layer thickness

Adsorbed Layer Thickness Results

Adsorbed layer thickness

Adsorbed layer thickness surfaces

Adsorbed layer thickness weight

Adsorbed layer, activity thickness

Alignment layer thickness

Amorphous layer thickness

Anisotropy layer-thickness dependence

Apparent layer thickness, determination

Bond layer thickness

Boundary layer thickness

Boundary layer thickness creeping flow

Boundary layer thickness cylinder

Boundary layer thickness dimensionless

Boundary layer thickness displacement

Boundary layer thickness flat plate

Boundary layer thickness fluid dynamics

Boundary layer thickness laminar flow, flat plate

Boundary layer thickness mass transfer

Boundary layer thickness momentum

Boundary layer thickness natural convection

Boundary layer thickness potential flow

Boundary layer thickness practical example

Boundary layer thickness stagnation point

Boundary layer thickness temperature

Boundary layer thickness thermal

Boundary layer thickness turbulent flow

Boundary layer thickness velocity

Boundary layers turbulent, thickness

Boundary-layer thickness definition

Brush layer thickness

Buffer layer thickness

Catalyst layer thickness

Chromium layer thickness

Consolidated layer thickness

Conversion catalyst layer thickness

Critical layer thickness

Crystalline layer thickness

D Layer thickness

Dead-layer thickness

Debye Length vs Diffusion Layer Thickness

Depletion layer thickness

Diffuse double layer thickness

Diffuse electrical double-layer thickness

Diffuse layer thickness, reducing

Diffuse layers thickness

Diffuse-reflection measurements sample-layer thickness

Diffusion layer of finite thickness

Diffusion layer of infinite thickness

Diffusion layer thickness

Diffusion layer thickness calculations

Diffusion layer thickness reduction

Diffusion layer time-dependent thickness

Diffusion-convection layer thickness

Dimensionless double layer thickness

Displacement thickness of boundary layer

Dissolution diffusion layer thickness

Double layer thickness

Double layer, capacitance/capacitor thickness

Double layer, electric thickness

Double layer: counter ions thickness

Double-layer thickness, equation defining

Dried layer, thickness

Effective layer thickness

Electrical double layer effective thickness

Electrical double layer thickness

Electrode Nemst diffusion layer, thickness

Elemental layer thicknesses, effect

Epitaxial layers critical thickness

Epitaxial layers thickness

Equilibrium grafted-layer thickness

Finite thickness, diffusion layer

Fluid laminar layer thickness

Gouy-Chapman layer thickness

Graft surface layer thickness

Granular layer thickness

Heat transfer boundary layer thickness

Hydrodynamic boundary layer thickness

Hydrodynamic diffusion layer, thickness

Hydrodynamic radius, layer thickness

Hydrodynamic thickness of adsorbed polymer layers

INTERFACIAL LAYER THICKNESS

Infinite thickness, diffusion layer

Interface layer thickness

Interfacial layer thickness and

Laminar boundary layer thickness

Layer Thickness and Plate Size

Layer thickness, definition

Layer thickness, polymeric stabilization

Layers, transcrystalline thickness

Low layer thickness

Lubricant layer thickness decreasing with

Magnetization layer-thickness dependence

Mass boundary layer thickness

Mass transfer boundary layer thickness dimensionless

Mass transport diffusion layer, thickness

Mass transport reaction layer thickness

Materials science thick layers

Matrimid active layer thickness

Membrane selective layer thickness

Metallizing layer thickness

Minerals layer thickness

Mobile phase layer thickness effects

Molten layer thickness

Mucous layer thickness

Multilayers layer thickness determination

Nemst diffusion layer thickness

Nernst diffusion layer thickness

Nernst diffusion layer thickness, rotating

Neutron reflectivity surface layer thickness

Nickel passive layer thickness

Online Measurement of Fouling Layer Thickness

Oxide layer thickness

Ozone layer thickness

Particle layer thickness

Penetration theory, boundary layer thickness

Poly layer thickness variations

Polymer films layer thickness

Polymer layer, thickness

Polymeric surfactants adsorbed layer thickness

Polymers adsorbed layer thickness

Polystyrene latex adsorbed layer thickness

Prandtl boundary layer/thickness

Purple layer thickness

RBS Spectra from Thin and Thick Layers

RBS spectrum from thick layers

Reaction layer thickness

Real-time fouling layer thickness

Reciprocal thickness of double layer

Results Obtained with Two Layers of Equal Thicknesses

Results with Three Layers of Equal and Different Thicknesses

Results with Two Layers of Different Relative Thicknesses

Root mean squar layer thickness

Root-mean-square layer thickness

Rotating disk electrode voltammetry diffusion layer thickness

Ruthenium layer thickness

Sample layer thickness

Scanning electron microscopy oxide layer thickness

Selection of layer thickness

Selective layer thickness

Shedding layer thickness

Shock layer thickness

Silicalite layer thickness

Smectic layer thickness

Soot layer thickness

Space charge layer thickness

Steady-state diffusion layer, thickness

Steric adsorbed layer thickness

Steric layer thickness

Stern layer thickness

Surface layer thickness

Surface layer, chemical potential thickness

Surface layers preparation thickness

Surface region electrical double layer thickness

Temperature adsorbed layer thickness

Thick Surface Charge Layer and Donnan Potential

Thick layers

Thick layers

Thick layers, rotational viscosity

Thick-layer chromatography

Thickness adsorbed protein layers

Thickness and Optical Properties of Layers on Solid Supports

Thickness determination of bituminous layers

Thickness determination of capping layer

Thickness diffusion boundary layer

Thickness muscle layer

Thickness of adsorbed layers

Thickness of adsorption layer

Thickness of diffusion boundary layer

Thickness of diffusion layer

Thickness of electric double layer

Thickness of insulating layer

Thickness of layers

Thickness of surface layer

Thickness of the Adsorbed Layer

Thickness of the Electric Double Layer

Thickness of the Enzyme Layer

Thickness of the Nernst diffusion layer

Thickness of the adsorbed polymer layer

Thickness of the diffusion boundary layer

Thickness of the diffusion layer

Thickness of the double layer

Thickness of the space charge layer

Thickness of wetting layer

Thickness, of oxide layers

Thickness, solvent layer

Thin or Thick Layer Chromatography (TLC)

Thin- and thick-layer methods

Transition layer thickness

Turbulent boundary layer displacement thickness

Unstirred water layer thickness

Viscosity thick electrical double layers

Zeta Potential Thick Electrical Double Layers

© 2024 chempedia.info