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Component equilibria

Prausnitz (12) applied the equation to the calculations of vapor/liquid phase equilibria. Component combination rules, interaction coefficients, and pseudo-criticals were all part of the extension of the equation to this new application. [Pg.343]

When the original compositions of the outer phases are different, the permselective membrane will prevent the complete leveling of these compositions. Some equilibrium component distribution between phases (a) and (p) will be established, and between points A and B a potential difference called the membrane potential (or transmembrane potential) (p will develop. This potential difference is determined by... [Pg.71]

H a phase r25). An external magnetic field induces new nonzero values of basic functions. Its have the same symmetry as corresponding components of a magnetic field. For instance, the equilibrium components Fx and... [Pg.234]

Windows PC at our fingertips anyway Each of us, however, does not have such software luxury, and in many cases we improvise our best solution for our process engineering needs. I have therefore proposed this simple but fully comprehensive and reliable K value derivation that I will call PPK, which stands for practical process K equilibrium component values. [Pg.40]

The reaction of carbohydrates in acid or alkaline solution results in a number of products, many of which have been identified over the past century (L/i). With the exception of anhydrosugars (e.g., l,6-anhydro-/ -D-glucopyranose) and oligosaccharides, which are concentration-dependent and equilibrium components (reversion products) formed in acid solution, all of these products result from reactions associated with the Lobry de Bryn-Alberda Van Ekenstein transformation or intermediates formed from this transformation. [Pg.277]

Nonequilibrium conditions may occur with respect to disturbances in the interior of a system, or between a system and its surroundings. As a result, the local stress, strain, temperature, concentration, and energy density may vary at each instance in time. This may lead to instability in space and time. Constantly changing properties cannot be described properly by referring to the system as a whole. Some averaging of the properties in space and time is necessary. Such averages need to be clearly stated in the utilization and correlation of experimental data, especially when their interpretations are associated with theories that are valid at equilibrium. Components of the generalized flows and the thermodynamic forces can be used to define the trajectories of the behavior of systems in time. A trajectory specifies the curve represented by the flow and force components as functions of time in the flow-force space. [Pg.599]

Andrews has suggested that the overall fracture energy. If, can be separated into reversible (equilibrium) and irreversible (non-equilibrium) components. This is represented by the Equation... [Pg.125]

At room temperature, 247 very rapidly shows an uptake of iodine corresponding to the complete oxidation of one thiol group. The oxidation product, the dimeric pyranose 249, is also formed by air oxidation of 247 on long standing of solutions thereof. Obviously, there exists, in addition to the favored thiofuranose form 247, a small proportion of the pyranose form 250 as an equilibrium component, and this has an easily oxidizable thiol group. By oxidation to the disulfide 249, this minor component of the equilibrium mixture is removed and, on rapid reattainment of the equilibrium, all of 247 becomes oxidized. The ready oxidizability of the thiol group of a 4-thiopyranose is likewise shown by the formation of bis(methyl 4-deoxy- 8-D-ribopyranoside-4-yl) 4,4 -disulfide by the air oxidation (iodine-catalyzed) of methyl 4-thio-)8-D-ribopyranoside. ... [Pg.222]

For stage 3, the component-material balance and equilibrium component i are as follows relationship for... [Pg.33]

Several different noble gas (particularly He) components can be present in natural waters. The information that we hope to obtain from the study of dissolved noble gases is related to the individual components. For instance, the radiogenic and tritiogenic He components contain age information, whereas the solubility equilibrium components of all noble gases may be used to derive the equilibration temperature. For the interpretation and use of dissolved noble gases, it is therefore necessary to evaluate the data in terms of individual components. In this section, we discuss techniques to separate the components contributing to the measured total noble gas concentrations and isotope ratios. [Pg.633]

Separation using all noble gases Iterative approaches. If the equilibrium component is unknown (e.g., beeause of unknown equilibration temperature) and excess air is present, we have for each noble gas at least two unknown components (equilibrium and excess air) in Equation (5). However, because both components have defined (although in general unknown) elemental eompositions, the equations are linked and can be solved. This is the typical situation in applications of the noble gas thermometer , where the equilibration temperature is to be derived from the concentrations of dissolved noble gases in ground water. [Pg.644]

It should however be stressed that each individual parameter of the equilibrium component can be well determined even in the presence of fractionated excess air. This fact provides the basis for the application of noble gas concentrations in ground water as indicators of paleotemperature. [Pg.649]

Consider, for instance, the system C-H-O. Even if the equilibrium components are limited to CH4, CO, CO2, H2 and H2O, when the total pressure p, the temperature and two stoichiometric parameters Zriii/Znc, ZnQ/Znc) are known, the following equations apply ... [Pg.1985]

Arts. Pure solids do not appear in the equilibrium constant expression. Therefore, = [NH3IHCI]. The stoichiometry of the reaction requires that, whatever the final concentrations of the equilibrium components, they must be equal to each other. We will let each concentration equal x, substitute that unknown into the equilibrium constant expression, and solve for the unknown ... [Pg.160]

Eisenman. G. Krasne. S. Ciani, S. The kinetic and equilibrium components of selective ionic permeability mediated by nactin- and valinomycin-type carriers having systematically varied degrees of methylation. Ann. N. Y. Acad. Sci. 1975. 264, 34-60. (Carriers Channels Biol. Syst.). [Pg.765]

Unlike Gi(t), the functions G2(t) and G3(t) contain non-zero equilibrium components,... [Pg.357]

Concentration of the solvate active solvent or the solvate active component A of mixed solvent in dilute solution is higher than the initial concentration of equilibrium components [E]o and [F]q. Then activity of equilibrium components is equal to their concentrations. Then equations of material balance for components A and B can be set down as... [Pg.534]

Solubility whieh is an equilibrium component describing the concentration of gas molecules within the membrane, that is the driving force, and Diffusivity, which is a dynamic component describing the mobility of the gas molecules within the membrane. [Pg.203]

Each of the electrode systems described above constitutes what is known as a half-ceir and it is necessary to couple two such half-cells to form a complete electrochemical cell. When all the equilibrium components of a half-cell are in their standard states of unit activity, the electrode is said to be Standard Electrode and to adopt its Standard Potential. [Pg.88]

NaOH is too weak a base to form a salt with the terminal alkyne. Of the equilibrium components with NaOH, the internal alkyne is favored since it is the most stable of these structures. Very small amounts of the allene and the terminal alkyne are formed. [Pg.144]


See other pages where Component equilibria is mentioned: [Pg.1741]    [Pg.252]    [Pg.517]    [Pg.263]    [Pg.20]    [Pg.21]    [Pg.127]    [Pg.137]    [Pg.2074]    [Pg.139]    [Pg.350]    [Pg.282]    [Pg.11]    [Pg.634]    [Pg.637]    [Pg.642]    [Pg.644]    [Pg.645]    [Pg.2062]    [Pg.1978]    [Pg.1745]    [Pg.403]    [Pg.87]    [Pg.147]    [Pg.399]   
See also in sourсe #XX -- [ Pg.40 , Pg.44 , Pg.49 ]




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Adsorption single-component equilibrium

Analytic Solution for Irreversible Equilibrium (One Adsorbable Component)

Calculation of Single Component Adsorption Equilibria

Component Balances and Equilibria

Component equilibria vapor-liquid

Component-equilibrium dead state

Components aqueous systems, chemical equilibrium

Components, rocks, soil equilibrium

Energy Transfer Equations in Multi-Component Quasi-Equilibrium Plasma-Chemical Systems

Equilibria in multiple-component systems

Equilibria in single-component systems

Equilibria of simple natural gas components

Equilibrium displacements in heterogeneous systems passage of a component from one phase to another

Equilibrium multi-component

Equilibrium-dispersive model single components

Experimental determination of phase equilibria in systems containing a near-critical component

Four-component mixtures phase equilibrium

Liquid Equilibria in Ternary Systems Containing One Supercritical Component

Liquid-Vapor Phase Equilibrium Curves for Individual Components

Multi-component calculations equilibria

Phase equilibria involving two-component systems partition

Phase equilibrium components

Phase equilibrium in single-component system

Phase equilibrium multi component mixtures

Principal equilibrium-determining component

Single-Component Equilibrium Isotherms

Single-Component Phase Equilibrium

Single-Component Profiles with the Equilibrium Dispersive Model

Single-component systems equilibria

Two-Component Band Profiles with the Equilibrium-Dispersive Model

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