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Estimation of the thickness

Equations (10.14) and (10.8) can be used for estimation of the thickness and mass coverage of the receptor adsorbed to the sensor surface and of the analyte layer bound to the receptor layer. [Pg.283]

In order to be able to include a steric contribution in the interparticle energy calculation, an estimate of the adsorbed layer thickness is required. This is very difficult to access experimentally probably the only technique which might be able to provide an estimate is small-angle neutron scattering which was beyond the scope of this work. As a result, a theoretical estimation of the thickness was made, based on a few key observations. This is described below. [Pg.61]

We may likewise obtain an estimate of the thickness of the adsorbed film by determining the maximum current density at which ions may be deposited at an electrode which is kept in rapid rotation. The ions being deposited must be regarded as migrating across a film of thickness S from a concentration equal to that in the bulk of the electrolyte to a region of zero concentration under the applied electromotive force. Thus Ackerberg Anorg. [Pg.193]

X 10 grm. ions per sq. cm. The solution contains 10 grm. ions per c.c., hence the slice thickness which must be denuded is 1 6 X 10 cms., since the tailing off is gradual in character this thickness is a minimum estimate of the thickness of the diffuse layer. [Pg.221]

The results described above, in particular the relation between ignition energy and temperature, suggest a thermal mechanism for the initiation. The light will not be absorbed in a uniform manner in the surface layers. However, a rough estimate of the thickness of the surface layer which is heated to the ignition temperature may be obtained by assuming that the whole of the surface layer is heated to a uniform temperature. If d is the thickness of this surface layer, then... [Pg.383]

A critical component of the cell is the X-ray-transparent window that allows the X-ray beam to impinge on the sample and the transmitted or fluorescent X-rays to be detected. Typical window materials that have been used are polyimide (Kapton ), beryllium, quartz, diamond, polyester (Mylar ), and titanium. Table 3 shows estimates of the thicknesses of window materials for various X-ray energies from 5 to 25 keV, determined on the basis of the assumption that 25% of the X-rays are absorbed by the window material. [Pg.371]

Diffusion time (diffusion time constant) — This parameter appears in numerous problems of - diffusion, diffusion-migration, or convective diffusion (- diffusion, subentry -> convective diffusion) of an electroactive species inside solution or a solid phase and means a characteristic time interval for the process to approach an equilibrium or a steady state after a perturbation, e.g., a stepwise change of the electrode potential. For onedimensional transport across a uniform layer of thickness L the diffusion time constant, iq, is of the order of L2/D (D, -> diffusion coefficient of the rate-determining species). For spherical diffusion (inside a spherical volume or in the solution to the surface of a spherical electrode) r spherical diffusion). The same expression is valid for hemispherical diffusion in a half-space (occupied by a solution or another conducting medium) to the surface of a disk electrode, R being the disk radius (-> diffusion, subentry -> hemispherical diffusion). For the relaxation of the concentration profile after an electrical perturbation (e.g., a potential step) Tj = L /D LD being - diffusion layer thickness in steady-state conditions. All these expressions can be derived from the qualitative estimate of the thickness of the nonstationary layer... [Pg.156]

SAIE by low-pressure plasma polymerization of TMS was extended to pure iron [8]. Polished pure iron samples (3x3 cm) were plasma pretreated before deposition of TMS plasma polymer. Two to six samples of pure iron were placed on a CRS plate (15 X 10 cm) maintaining the electrical contact so that each pure iron sample acts as the cathode of DC discharge. A few small pieces of silicon water were also placed on the CRS plate to maintain the electrical contact and were used for the estimation of the thickness of TMS plasma polymer by ellipsometry. [Pg.732]

Figure 6 P-T arrays compiled for garnet peridotite xenoliths from several suites using two-pyroxene thermometry and Al-in-orthopyroxene barometry (Tbkn and Rbkn methods, Table 5). Data sources given in Rudnick and Nyblade with additional data here for Vitim (Ionov et al., 1993a) and Canada (MacKenzie and Canil, 1999 Schmidberger and Francis, 1999). The best-fit line for the Kaapvaal data is plotted in each figure for reference. Intersection of P-T array with mantle adiabats (shaded field) represents an estimate of the thickness of lithosphere at the time of sampling. Figure 6 P-T arrays compiled for garnet peridotite xenoliths from several suites using two-pyroxene thermometry and Al-in-orthopyroxene barometry (Tbkn and Rbkn methods, Table 5). Data sources given in Rudnick and Nyblade with additional data here for Vitim (Ionov et al., 1993a) and Canada (MacKenzie and Canil, 1999 Schmidberger and Francis, 1999). The best-fit line for the Kaapvaal data is plotted in each figure for reference. Intersection of P-T array with mantle adiabats (shaded field) represents an estimate of the thickness of lithosphere at the time of sampling.
The estimation of the thickness of the water layer affected by the presence of a solute molecule was made for two geometries (1) the cavity containing the solute and the correlation volume have the shape of a sphere, (2) both have the shape of a cylinder. The results of the calculations are listed in Table 7, which shows that the water layer is formed of several molecular shells (between 4 and 8, Table 7). The correlation volumes for cyclic hydrocarbon are much lower than for aliphatic hydrocarbons, but, among the cychc hydrocarbons, the... [Pg.20]

J. N. Wilson (Shell Development Company) I should like to inquire whether Dr. Cranston (Lecture 17) has considered correcting his estimates of the thickness of the adsorbed multilayers for the radius of curvature of the capillary on whose walls it is being formed. The correction can be quite appreciable for pores whose apparent radius is 50 A. or less. [Pg.168]

Let us first make a rough estimate of the thickness by assuming that there are no positive ions (coions) present. Then the electric potential from the Poisson equation (Eqs. 3.4.5 and 3.4.7) is defined by... [Pg.387]

It is clear that values for the interfacial surface concentrations, Cas and Cws, could not be obtained, neither could estimates of the thickness of the films, Za and z -The dimensionless Henry s law constant H defines the distribution across the water air interface and. [Pg.131]

The schematic diagram of Figure 1-21 illustrates the internal structure of cuticle cells. Each cuticle cell contains a thin outer membrane, the epicuti-cle. Different estimates of the thickness of this membrane have been cited (25 to 250 angstroms) however, 50 to 100 angstroms is probably the most common estimate [62, 63]. Beneath the cuticle cell membranes are three major layers the A layer, a resistant layer with a high cystine content... [Pg.27]

The thickness of a protein hydration shell has long been an object of study, and also a topic of lively debate. However, even this apparently simple question cannot be answered in a straightforward way. Estimates of the thickness of the hydration shell vary from one to two monolayers to 10 monolayers, depending on the experimental probe used. [Pg.118]

An estimation of the thickness of the diffusion layer can be obtained through the Nernst diffusion layer, 6 (m), defined as shown in Figure 1.3. For the Cottrell experiment under linear diffusion conditions the 6 value for a species j is given by... [Pg.9]

A THERMODYNAMIC ESTIMATE OF THE THICKNESS OF THE SURFACE LAYER OF LIQUIDS. [Pg.179]

P(3) When the thickness of the matrix resin layer acting as an adhesive layer cannot be defined, a representative estimate of the thickness value shall be given by the designer, see 5.3.6.1. [Pg.195]

It is practically impossible to define the actual bondline thickness. Therefore one has to make an estimate of the thickness. In most cases it is beneficial for the joint strength to have a thin bond layer. However, an unrealistically low estimate of the bond layer thickness should not be made. A realistic minimum value is 0.1 mm. [Pg.487]

A button case for a small battery must be silver coated. The button is a perfect cylinder with a radius of 3.0 mm and a height of 2.0 mm. For simplicity, assume that the silver solution used for plating is silver nitrate. (Industrial processes often use other solutions.) Assume that the silver plating is perfectly uniform and is carried out for 3.0 min at a current of 1.5 A, (a) What mass of silver is plated on the part (b) How many atoms of silver have plated on the part (c) Calculate an estimate of the thickness (in atoms) of the silver coating. (Silver has a density of 10.49 g/cm and an atomic radius of 160 pm.)... [Pg.575]


See other pages where Estimation of the thickness is mentioned: [Pg.267]    [Pg.97]    [Pg.180]    [Pg.30]    [Pg.99]    [Pg.224]    [Pg.141]    [Pg.12]    [Pg.518]    [Pg.211]    [Pg.283]    [Pg.1704]    [Pg.429]    [Pg.73]    [Pg.740]    [Pg.180]    [Pg.438]    [Pg.199]    [Pg.518]    [Pg.180]    [Pg.367]    [Pg.76]    [Pg.120]    [Pg.57]    [Pg.5806]   


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