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Wetting isotherm

Transient experiments were expected to yield a smooth transition between the observed dry and wet equilibrium states In Figures 2a, 2b, 3a, and 3b. However, this expected behavior was restricted to a relatively short time segment following the Initial change from a dry to a wet Isothermal environment. It Is... [Pg.103]

The four vertical lines on the diagram show the isothermal depletion loci for the main types of hydrocarbon gas (incorporating dry gas and wet gas), gas condensate, volatile oil and black oil. The starting point, or initial conditions of temperature and pressure, relative to the two-phase envelope are different for each fluid type. [Pg.102]

There are complexities. The wetting of carbon blacks is very dependent on the degree of surface oxidation Healey et al. [19] found that q mm in water varied with the fraction of hydrophilic sites as determined by water adsorption isotherms. In the case of oxides such as Ti02 and Si02, can vary considerably with pretreatment and with the specific surface area [17, 20, 21]. Morimoto and co-workers report a considerable variation in q mm of ZnO with the degree of heat treatment (see Ref. 22). [Pg.349]

This description is traditional, and some further comment is in order. The flat region of the type I isotherm has never been observed up to pressures approaching this type typically is observed in chemisorption, at pressures far below P. Types II and III approach the line asymptotically experimentally, such behavior is observed for adsorption on powdered samples, and the approach toward infinite film thickness is actually due to interparticle condensation [36] (see Section X-6B), although such behavior is expected even for adsorption on a flat surface if bulk liquid adsorbate wets the adsorbent. Types FV and V specifically refer to porous solids. There is a need to recognize at least the two additional isotherm types shown in Fig. XVII-8. These are two simple types possible for adsorption on a flat surface for the case where bulk liquid adsorbate rests on the adsorbent with a finite contact angle [37, 38]. [Pg.618]

Many of the unusual properties of the perfluorinated inert fluids are the result of the extremely low intermolecular interactions. This is manifested in, for example, the very low surface tensions of the perfluorinated materials (on the order of 9-19 mN jm. = dyn/cm) at 25°C which enables these Hquids to wet any surface including polytetrafluoroethene. Their refractive indexes are lower than those of any other organic Hquids, as are theh acoustic velocities. They have isothermal compressibilities almost twice as high as water. Densities range from 1.7 to 1.9 g/cm (l )-... [Pg.297]

As an example of using a Mollier diagram in defining the state of air, we can take a typical measurement from the local exhaust hood of a paper machine. Tbe temperature of the exhaust air is 82 C and its wet bulb temperature 60 "C. In Fig. 4AQd we move from the saturation curve at the point 60 °C straight up along the constant enthalpy line ( = 460 kj/kg d.a.) until we reach the isotherm... [Pg.91]

In Fig. 15 we show similar results, but for = 10. Part (a) displays some examples of the adsorption isotherms at three temperatures. The highest temperature, T = 1.27, is the critical temperature for this system. At any T > 0.7 the layering transition is not observed, always the condensation in the pore is via an instantaneous filling of the entire pore. Part (b) shows the density profiles at T = 1. The transition from gas to hquid occurs at p/, = 0.004 15. Before the capillary condensation point, only a thin film adjacent to a pore wall is formed. The capillary condensation is now competing with wetting. [Pg.225]

We can conclude that the stability of static foam in porous media depends on the medium permeability and wetting-phase saturation (i.e., through the capillary pressure) in addition to the surfactant formulation. More importantly, these effects can be quantified once the conjoining/disjoining pressure isotherm is known either experimentally (8) or theoretically (9). Our focus... [Pg.466]

To determine any structure modification to the Degussa C-aluminoxide support during wet impregnation and calcinations, adsorption/desorption isotherms obtained before and after modifications were compared. The results as presented in Figure 14.1 are in agreement with our previous results.39 It is found that the... [Pg.251]

Trapaga and Szekely 515 conducted a mathematical modeling study of the isothermal impingement of liquid droplets in spray processes using a commercial CFD code called FLOW-3D. Their model is similar to that of Harlow and Shannon 397 except that viscosity and surface tension were included and wetting was simulated with a contact angle of 10°. In a subsequent study, 371 heat transfer and solidification phenomena were also addressed. These studies provided detailed... [Pg.385]

Hysteresis is observed not only in the sorption isotherms but also in calorimetric measurements of heat of wetting at different moisture contents, and it is thus a combined entropy and enthalpy phenomenon. A reliable explanation for this effect is not currently available, but there is speculation that it is due to the stresses which are induced as the cellulose swells. Since the swelling of cellulose is not completely reversible, mechanical recovery is incomplete and hysteresis will therefore be present both in the internal stress-strain curve of the sample, and also in the water adsorption isotherm. [Pg.76]

Fig. 50. TG curve showing the formation of alumina whiskers during oxidation of iron-aluminum alloy in wet hydrogen (2%)/argon mixture (isothermal at 1555 °C). Sample weight 1000 mg... Fig. 50. TG curve showing the formation of alumina whiskers during oxidation of iron-aluminum alloy in wet hydrogen (2%)/argon mixture (isothermal at 1555 °C). Sample weight 1000 mg...
We review Monte Carlo calculations of phase transitions and ordering behavior in lattice gas models of adsorbed layers on surfaces. The technical aspects of Monte Carlo methods are briefly summarized and results for a wide variety of models are described. Included are calculations of internal energies and order parameters for these models as a function of temperature and coverage along with adsorption isotherms and dynamic quantities such as self-diffusion constants. We also show results which are applicable to the interpretation of experimental data on physical systems such as H on Pd(lOO) and H on Fe(110). Other studies which are presented address fundamental theoretical questions about the nature of phase transitions in a two-dimensional geometry such as the existence of Kosterlitz-Thouless transitions or the nature of dynamic critical exponents. Lastly, we briefly mention multilayer adsorption and wetting phenomena and touch on the kinetics of domain growth at surfaces. [Pg.92]


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See also in sourсe #XX -- [ Pg.172 ]




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