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Surface covering

Langmuir adsorption isotherm A theoretical equation, derived from the kinetic theory of gases, which relates the amount of gas adsorbed at a plane solid surface to the pressure of gas in equilibrium with the surface. In the derivation it is assumed that the adsorption is restricted to a monolayer at the surface, which is considered to be energetically uniform. It is also assumed that there is no interaction between the adsorbed species. The equation shows that at a gas pressure, p, the fraction, 0, of the surface covered by the adsorbate is given by ... [Pg.234]

Clearly, the physical chemistry of surfaces covers a wide range of topics. Most of these subjects are sampled in this book, with emphasis on fundamentals and important theoretical models. With each topic there is annotation of current literature with citations often chosen because they contain bibliographies that will provide detailed source material. We aim to whet the reader s appetite for surface physical chemistry and to provide the tools for basic understanding of these challenging and interesting problems. [Pg.3]

Fig. VIII-10. (a) Intensity versus energy of scattered electron (inset shows LEED pattern) for a Rh(lll) surface covered with a monolayer of ethylidyne (CCH3), the structure of chemisorbed ethylene, (b) Auger electron spectrum, (c) High-resolution electron energy loss spectrum. [Reprinted with permission from G. A. Somoijai and B. E. Bent, Prog. Colloid Polym. ScL, 70, 38 (1985) (Ref. 6). Copyright 1985, Pergamon Press.]... Fig. VIII-10. (a) Intensity versus energy of scattered electron (inset shows LEED pattern) for a Rh(lll) surface covered with a monolayer of ethylidyne (CCH3), the structure of chemisorbed ethylene, (b) Auger electron spectrum, (c) High-resolution electron energy loss spectrum. [Reprinted with permission from G. A. Somoijai and B. E. Bent, Prog. Colloid Polym. ScL, 70, 38 (1985) (Ref. 6). Copyright 1985, Pergamon Press.]...
Fig. X-3. Variation of contact angle with /oh. the fraction of the surface covered by HS(CH2)uOH in a mixture with HS(CH2)uCH3. Solid line is comparison with Eq. X-27, and dashed line is from Eq. X-28. (From Ref. 44.)... Fig. X-3. Variation of contact angle with /oh. the fraction of the surface covered by HS(CH2)uOH in a mixture with HS(CH2)uCH3. Solid line is comparison with Eq. X-27, and dashed line is from Eq. X-28. (From Ref. 44.)...
While a thermodynamic treatment can be developed entirely in terms of f(P,T), to apply adsorption models, it is highly desirable to know on a per square centimeter basis rather than a per gram basis or, alternatively, to know B, the fraction of surface covered. In both the physical chemistry and the applied chemistry of the solid-gas interface, the specific surface area is thus of extreme importance. [Pg.571]

Since S /S equals 6, the fraction of surface covered, Eq. XVII-4 can be written in the form... [Pg.604]

The basic assumption is that the Langmuir equation applies to each layer, with the added postulate that for the first layer the heat of adsorption Q may have some special value, whereas for all succeeding layers, it is equal to Qu, the heat of condensation of the liquid adsorbate. A furfter assumption is that evaporation and condensation can occur only from or on exposed surfaces. As illustrated in Fig. XVII-9, the picture is one of portions of uncovered surface 5o, of surface covered by a single layer 5, by a double-layer 52. and so on.f The condition for equilibrium is taken to be that the amount of each type of surface reaches a steady-state value with respect to the next-deeper one. Thus for 5o... [Pg.619]

Figure Bl.19.13. (a) Tliree STM images of a Pt(l 11) surface covered witli hydrocarbon species generated by exposure to propene. Images taken in constant-height mode. (A) after adsorption at room temperature. The propylidyne (=C-CH2-CH2) species that fomied was too mobile on the surface to be visible. The surface looks similar to that of the clean surface. Terraces ( 10 mn wide) and monatomic steps are the only visible features. (B) After heating the adsorbed propylidyne to 550 K, clusters fonn by polymerization of the C H... Figure Bl.19.13. (a) Tliree STM images of a Pt(l 11) surface covered witli hydrocarbon species generated by exposure to propene. Images taken in constant-height mode. (A) after adsorption at room temperature. The propylidyne (=C-CH2-CH2) species that fomied was too mobile on the surface to be visible. The surface looks similar to that of the clean surface. Terraces ( 10 mn wide) and monatomic steps are the only visible features. (B) After heating the adsorbed propylidyne to 550 K, clusters fonn by polymerization of the C H...
Miller A R 1946 The variation of the dipole moment of adsorbed particles with the fraction of the surface covered Proc. Camb.Phil. See. 42 292-303... [Pg.1898]

The model implies that at any pressure below the saturation vapour pressure, the fractions of the surface covered with 1, 2,. .., i molecules will be 6 02,.., 0i respectively, so that the thickness of the adsorbed layer will not be constant throughout. On the specific surface area A, therefore, the total number Z of molecules adsorbed will be... [Pg.43]

Draperies. Draperies of light weight or open-weave fabrics are ineffective for sound-absorbing purposes. Heavy draperies, such as flannel and velour, can provide useful sound absorption if properly installed. For best results they should be hung with 100% fullness, ie, 2 nC for every nC of wall or window surface covered. The sound-absorbing properties also are affected by the amount of space between the draperies and the surface behind them. [Pg.314]

In the simplest case, for which all adsorption sites are equivalent and do not interact with each other, the fraction of surface covered by adsorbate. [Pg.547]

Surface Coverage. The surface-covering abiHty of deposition techniques is best when the materials are deposited from a vapor or from a fluid having no need for an appHed voltage. The macroscopic and microscopic surface coverage of a thin film deposited by PVD techniques on a substrate surface may be improved by the use of gas scattering and concurrent bombardment during film deposition. [Pg.529]

Variable Variable ft e t/t, reduced time, fraction of surface covered by adsorbed ... [Pg.682]

Adsorptive Equilibrium The fraction of the surface covered by A at equilibrium is... [Pg.691]

This criterion is derived from the fact that the free corrosion potential in soil is generally I/cu Cuso4 -0-55 V. Ohmic voltage drop and protective surface films are not taken into consideration. According to the information in Chapter 4, a maximum corrosion rate for uniform corrosion in soil of 0.1 mm a can be assumed. This corresponds to a current density of 0.1 A m l In Fig. 2-9, the corrosion current density for steel without surface film changes by a factor of 10 with a reduction in potential of about 70 mV. To reduce it to 1 jum a (0.14 V would be necessary. The same level would be available for an ohmic voltage drop. With surfaces covered with films, corrosion at the rest potential and the potential dependence of corrosion in comparison with act contrary to each other so that qualitatively the situation remains the same. More relevant is... [Pg.104]

As an example, consider again the back surface of the silicon wafer used in the mechanical profiler example. Eigure 4a, an SEM micrograph taken at 45° tilt, shows a surface covered with various sized square-shaped features that often overlap. This information cannot be discerned from the mechanical profiler trace, but can be obtained using a 3D optical profiler measurement. Eigures 4b and 4c are also... [Pg.701]

Let the concentration of solvent (B) in equilibrium with the silica gel surface be (c) g/ml. Let a fraction (a) of the surface be covered with a mono-layer of the polar solvent (B) and, of that fraction (a), let a fraction ( 3) be covered by a second layer of the polar solvent (B). The number of molecules striking and adhering to the surface covered with a mono-layer of polar solvent (A) and that covered with a mono-layer of solvent (B) per unit time will be (n ) and be (n") respectively. Furthermore, let the number of molecules of solvent (A) leaving the mono-layer surface and the bi-layer surface per unit time be ni and 2 respectively. Now, under conditions of equilibrium,... [Pg.95]

Fig. 34. PAA aluminum surface covered with a thin layer of grease that masks the oxide morphology. Fig. 34. PAA aluminum surface covered with a thin layer of grease that masks the oxide morphology.
Many different types of tables exhaust downwards and have a perforated surface covering part of the table, e.g., inside a cabinet. This design is common in biological safety cabinets (see Section 10.4.6.4). Biological safety cabinets use a combination of a supply and an exhaust opening, and therefore are not defined a.s a downdrafr table. [Pg.875]

Frasch process for mining sulfur. Superheatad watar at 165°C is sent down through the outer pipe to form a pool of molten sulfur (mp = 119°C) at the base. Compressed air, pumped down the inner pipe, brings the sulfur to the surface. Sulfur deposits are often 100 m or more beneath the earth s surface, covered with quicksand and rock. [Pg.558]

The addition of some metal ions, such as Mg2+,Zn2+, In3+,orGa3+, and some organic additives, such as 2-thiophene, 2-methylfuran, or benzene, to propylene carbonate-LiC104 improved the coulombic efficiency for lithium cycling [112]. Lithium deposition on a lithium surface covered with a chemically stable, thin and tight layer which was formed by the addition of HF to electrolyte can suppress the lithium dendrite formation in secondary lithium batteries [113]. [Pg.58]

Davies et al. (D9) have recently measured the rates of absorption of various gases into turbulently stirred water both with carefully cleaned surfaces and with surfaces covered with varying amounts of surfactants. That hydrodynamic resistances, rather than monolayer resistances, are predominant in their work is consistent with the high sensitivity of kL to very small amounts of surface contamination and also with the observation that a limit to the reduction in kL is found (D7, D9). This is in agreement with the results of Lindland and Terjesen (L9), who found that after a small concentration of surfactant had been used further additions caused but little change in terminal velocity (L9). [Pg.332]

M. Ayyoob, and M.S. Hegde, An XPS study of the adsorption of oxygen on silver and platinum surfaces covered with potassium or cesium, Surf. Sci. 133, 516-532 (1983). [Pg.86]


See other pages where Surface covering is mentioned: [Pg.175]    [Pg.411]    [Pg.655]    [Pg.915]    [Pg.946]    [Pg.1688]    [Pg.2377]    [Pg.280]    [Pg.565]    [Pg.117]    [Pg.691]    [Pg.268]    [Pg.427]    [Pg.119]    [Pg.51]    [Pg.13]    [Pg.445]    [Pg.1085]    [Pg.113]    [Pg.826]    [Pg.697]    [Pg.132]    [Pg.807]    [Pg.135]    [Pg.344]    [Pg.15]    [Pg.129]   


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Adsorbate-covered surfaces, scanning

Adsorbate-covered surfaces, scanning tunneling microscopy

Apparent Surface Free Energy Calculated for Glass Plates Covered with Pure PS Layers

Apparent surface free energy plates covered with

Clean surface covers

Cover zones, surface treatments

Covering surface impoundments

Decorative surface coverings

Ellipsometry Equations for Film-Covered Surfaces

Fraction of Surface Covered

Hydrogen nickel surface covering

Hydrogen tungsten surface covering

Oxygen surface covering

Polymer-covered surfaces, steric force

Promoters surface covering

Surface film covered

Surface partially covered with adsorbed gases

Two Parallel Plates Covered with Surface Layers

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