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Vapors, interactive

Cobalt vapor interacts with norbornene to produce Co(C7H10)3, a 15-electron complex, apparently isostructural with Ni(C7H10)3. The cobalt complex is soluble in hydrocarbon solvents to afford deep blue solutions decomposing rapidly and autocatalytically at -15° (5a, 134). It has not yet been possible to isolate this complex in a pure state but some of the reactions have been examined by trapping experiments ... [Pg.62]

In compact geometries the heat transfer coefficient depends on the two-phase flow pattern (51-67). For low condensation rates, the heat transfer is gravity controlled, and the heat transfer coefficient depends on the liquid film thickness. For higher condensation rates, the heat transfer coefficient depends on the vapor shear effect, and for small passages the liquid-vapor interaction leads to high heat transfer coefficients. [Pg.157]

As mentioned at the beginning of this chapter, besides thermal energy to produce atoms, there are chemical methods for obtaining atomic or molecular vapors that are readily atomizable. The atoms generated from these vapors interact with electromagnetic radiation, and the resulting atomic absorption or fluorescence phenomena can be monitored or else they can be excited and their... [Pg.273]

The fugacity coefficients are calculated using a simplified equation of state described earlier 4,6). For this treatment the constants b and Oi are calculated by knowing the critical temperature and pressure. The attraction coefficient ° is given by generalized coefficients for nonpolar substances and with two other individual constants for polar substances. If Yi refers tp the vapor composition and n refers to binary vapor interactions, the equation becomes... [Pg.76]

The process of water vapor interaction with amorphous solids has been likened to the production of a solid solution in which the water is dissolved in the solid matrix. As more water is absorbed, the fundamental properties of this solid matrix (e.g., viscosity) can undergo significant change that can then result in visually apparent changes in physical properties (e.g., collapse, recrystallization). This will be discussed in further detail later. [Pg.4052]

Sorption and diffusion in polymers are of fundamental and practical concern. However, data acquisition by conventional methods is difficult and time consuming. Again, IGC represents an attractive alternative. Shiyao and co-workers, concerned with pervaporation processes, use IGC to study adsorption phenomena of single gases and binary mixtures of organic vapors on cellulosic and polyethersulfone membrane materials (13). Their work also notes certain limitations to IGC, which currently restrict its breadth of application. Notable is the upper limit to gas inlet pressure, currently in the vicinity of 100 kPa. Raising this limit would be beneficial to the pertinent use of IGC as an indicator of membrane-vapor interactions under conditions realistic for membrane separation processes. [Pg.4]

The shapes of these isotherms are controlled by surface heterogeneity, and thus provide a means of deducing the various modes of interfacial attraction presented by the substrates. Isotherms of pentane on unsized IM6 before and after plasma treatment are congruent. Pentane interacts only by dispersion force attraction, as does methylene iodide the registry of these isotherms is predicted by the similarity in ft obtained from wetting measurements. Pentane isotherms serve as a reference with which to assess the effect of additional modes of solid/vapor interaction with acidic and basic probes. [Pg.211]

Solid-Liquid-Vapor Interactions in Alkali-Rich Coal Slags... [Pg.277]

COOK AND HASTIE Solid-Liquid- Vapor Interactions in Slags... [Pg.279]

Excellent instrumentation support and advice is available through Surface Measurement Systems (SMS) (1), manufacturer of DVS-Advantage and DVS-1000 and 2000 series of equipment for d3mamic vapor interaction studies. The DVS-FIT... [Pg.246]

Estimation of the Effective Hamaker Constant for Solid-Vapor Interactions for Different Soils. The Hamaker constant represents interactions between macro-objects such as mineral surfaces and liquid due to short-range (< 100A) van der Waals forces (Ackler et al., 1996 Bergstrom, 1997). The presence of van der Waals surfacial interactions in most liquid adsorption processes in nalural porous media renders the proper estimation of the Hamaker constant an important task. The Hamaker constant for liquid-liquid interactions through the intervening vapor is a... [Pg.22]

We proceed with illustrative examples for application of the proposed up-scaling scheme to seven soil types with properties listed in Table 1-2. The closed-form solution for degree of saturation (Eq. [23]) was fitted to measured data by optimizing parameters p, go, X, and the chemical potential pd at air entry point (that defines Lmax). Note that the Hamaker constant was estimated beforehand, as described in Estimation of the Effective Hamaker Constant for Solid-Vapor Interactions for Different Soils above. The estimated parameters were then used to calculate the liquid-vapor interfacial area for each soil (Eq. [28]). We used square shaped central pores for all soil types except the artificial sand mixture, where triangular pores were applied to emphasize capillaiy processes over adsorption in sand. I lowcver, the closed-form solutions for retention and interfacial area were derived lo accommodate any regular polygon-shaped central pore. Constants for various shapes are described in Table I-1. The values of primary physical constants employed in (he calculations and (heir units are shown in Table 1-3. [Pg.23]

Asvl = Hamaker constant for solid vapor interactions through intervening liquid (J) Aw = Liquid occupied area (m2)... [Pg.47]

A number of atmospheric gases and vapors interact with water to form ions upon dissolution. Most important among them are S02, C02, NH3, HC1, and HN03. Their reactions with water are reversible, and equilibrium conditions are again set up in clouds. Table 8-3 summarizes the reactions involved and the associated equilibrium constants. Rate coefficients for the individual forward and reverse reactions are included in Table 8-3 as far as they are known. These reactions are very fast, leading to time constants of the order of microseconds or less in establishing the equilibria. As Table 8-3 shows, the dissolution of reactive gases proceeds in two steps. The first... [Pg.394]

Frequently, colorless or nonfluorescent spots can be visualized by exposing the developed plate to iodine vapor. The iodine vapor interacts with the sample components, either chemically or by solubility, to produce a color. Thin-layer plates and sheets are commercially available that incorporate a fluorescent dye in the powdered adsorbent. When held under ultraviolet light, dark spots appear where sample spots occur due to quenching of the plate fluorescence. [Pg.629]

It appears, however, that since the difference y yo - y L is involved, this quantity may be capable of definition independently of the question of whether the solid surface itself is an equilibrium one. From a molecular point of view, the matter becomes one of estimating the difference between solid-liquid and solid-vapor interactions, and two simple models were considered. They are capable of at least some experimental reinforcements in the form of vapor adsorption studies, and... [Pg.70]


See other pages where Vapors, interactive is mentioned: [Pg.347]    [Pg.92]    [Pg.66]    [Pg.124]    [Pg.380]    [Pg.381]    [Pg.785]    [Pg.6]    [Pg.199]    [Pg.81]    [Pg.12]    [Pg.101]    [Pg.294]    [Pg.278]    [Pg.214]    [Pg.3]    [Pg.92]    [Pg.363]    [Pg.227]    [Pg.514]    [Pg.7]    [Pg.7]    [Pg.23]    [Pg.786]    [Pg.256]    [Pg.153]   
See also in sourсe #XX -- [ Pg.321 , Pg.322 ]




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