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Pressure-composition

The purpose of all flux models is to express the fluxes in a porous medium in terms of gradients in pressure, composition and temperature. Isothermal flux models are therefore all of the general form... [Pg.88]

The boiling point increases regularly. The boiling point - composition diagram for such a system is shown in Fig. 1, 4, 2 (the complementary vapour pressure - composition diagram is depicted in Fig. I, 4, 3 for purposes of comparison only). Let us consider the behaviour of such a liquid pair upon distillation. If a solution of composition is heated, the vapour pressure will rise until at the point ij it is equal to the pressure of the atmosphere, and boiling commences at temperature The com-... [Pg.8]

To appreciate the action of a drying agent of class (a), let us imagine some anhydrous copper sulphate in an evacuated vessel provided with a pressure gauge, and water is allowed to enter slowly the temperature is assumed constant at 25°. The results may be best expressed by means of a vapour pressure - composition diagram (Fig. 7, 20, 1). The initial system is represented by the point A the pressure will rise along AB until the monohydrate CuS04,H20 commences to form at B. [Pg.40]

Fig. 7. Pressure—composition relationships for the FeTi—H system at 40°C during formation of the hydride (o) and release of hydrogen ( ). Fig. 7. Pressure—composition relationships for the FeTi—H system at 40°C during formation of the hydride (o) and release of hydrogen ( ).
The pressure/composition requirement for miscibility limits the oil reservoirs in which this technology has been appHed. However, the low iajected fluid viscosity often results in poor volumetic sweep efficiency. [Pg.189]

In order to operate a process facility in a safe and efficient manner, it is essential to be able to control the process at a desired state or sequence of states. This goal is usually achieved by implementing control strategies on a broad array of hardware and software. The state of a process is characterized by specific values for a relevant set of variables, eg, temperatures, flows, pressures, compositions, etc. Both external and internal conditions, classified as uncontrollable or controllable, affect the state. Controllable conditions may be further classified as controlled, manipulated, or not controlled. Excellent overviews of the basic concepts of process control are available (1 6). [Pg.60]

Determine how each varies with temperature, pressure, composition, etc. [Pg.450]

Separation operations achieve their objective by the creation of two or more coexisting zones which differ in temperature, pressure, composition, and/or phase state. Each molecular species in the mixture to be separated reacts in a unique way to differing environments offered by these zones. Consequently, as the system moves toward equilibrium, each species establishes a different concentration in each zone, and this results in a separation between the species. [Pg.1242]

The first two examples show that the interaction of the model parameters and database parameters can lead to inaccurate estimates of the model parameters. Any use of the model outside the operating conditions (temperature, pressures, compositions, etc.) upon which the estimates are based will lead to errors in the extrapolation. These model parameters are effec tively no more than adjustable parameters such as those obtained in linear regression analysis. More comphcated models mav have more subtle interactions. Despite the parameter ties to theoiy, tliey embody not only the uncertainties in the plant data but also the uncertainties in the database. [Pg.2556]

In most cases, systems deviate to a greater or lesser extent from Raoult s law, and vapour pressures may be greater or less than the values calculated. In extreme cases (e.g. azeotropes), vapour pressure-composition curves pass through maxima or minima, so that attempts at fractional distillation lead finally to the separation of a constantboiling (azeotropic) mixture and one (but not both) of the pure species if either of the latter is present in excess. [Pg.9]

Evaporator and condenser pressure, composition of compressed vapor, size of compressor, and weight of charge required. [Pg.333]

The pair of Eqs. 12, 13 epitomizes the relation between the equilibrium vapor pressure, composition, and chemical potential of the solvent in a clathrate obeying the present model. These expressions were used in the calculation of the thermodynamic properties of gas hydrates30 and have also been formulated by Barrer and Stuart 4 for a clathrate with a single type of cavity and one occluded component they reduce to the equations of ref. 52. [Pg.15]

Figure 1. Ideal pressure-composition isotherms showing the hydrogen solid-solution phase, a, and the hydride phase, j3. The plateau marks the region of coexistence of the a and fl phases. As the temperature is increased the plateau narrows and eventually disappears at some consolule temperature... Figure 1. Ideal pressure-composition isotherms showing the hydrogen solid-solution phase, a, and the hydride phase, j3. The plateau marks the region of coexistence of the a and fl phases. As the temperature is increased the plateau narrows and eventually disappears at some consolule temperature...
There are few systematic guidelines which can be used to predict the properties of AB2 metal hydride electrodes. Alloy formulation is primarily an empirical process where the composition is designed to provide a bulk hydride-forming phase (or phases) which form, in situ, a corrosion— resistance surface of semipassivating oxide (hydroxide) layers. Lattice expansion is usually reduced relative to the ABS hydrides because of a lower VH. Pressure-composition isotherms of complex AB2 electrode materials indicate nonideal behaviour. [Pg.228]

In the major catalytic processes of the petroleum and chemical industries, continuous and steady state conditions are the rule where the temperature, pressure, composition, and flow rate of the feed streams do not vary significantly. Transient operations occur during the start-up of a unit, usually occupying a small fraction of the time of a cycle from start-up to shut-down for maintenance or catalyst regeneration. [Pg.63]

Low-detonation pressure composites consisting of PETN (and other expls) in a low-density (foam) plastic matrix (eg polyurethanes) are described by Abegg et al (Ref 33)... [Pg.570]

C, which leads to a break in the pressure-composition curve at BF3 Ir = 2 1. The formation of the 1 1 complex in solution is indicated by titrations. Insertion of InCl into the Fe—Fe bond in boiling dioxane yields [T7 -C CO)2Fe]2lnCl in 55% yield. The only group-VIIA compound that forms an addition compound with a group-lIIB halide, namely with BF3, is [(i7 -Cp)2ReH]The formation of (t -Cp),ReH BF3 is established when (T7 -Cp),ReH is titrated tensimetrically in toluene with BF3 at 0°C. [Pg.56]

Any numerical experiment is not a one-time calculation by standard formulas. First and foremost, it is the computation of a number of possibilities for various mathematical models. For instance, it is required to find the optimal conditions for a chemical process, that is, the conditions under which the reaction is completed most rapidly. A solution of this problem depends on a number of parameters (for instance, temperature, pressure, composition of the reacting mixture, etc.). In order to find the optimal workable conditions, it is necessary to carry out computations for different values of those parameters, thereby exhausting all possibilities. Of course, some situations exist in which an algorithm is to be used only several times or even once. [Pg.776]

The residuals are functions of temperature, pressure, composition and the interaction parameters. These functions can easily be derived analytically for any equation of state. At equilibrium the value of these residuals should be equal to zero. However, when the measurements of the temperature, pressure and mole fractions are introduced into these expressions the resulting values are not zero even if the EoS were perfect. The reason is the random experimental error associated with each measurement of the state variables. [Pg.256]

In part II of the present report the nature and molecular characteristics of asphaltene and wax deposits from petroleum crudes are discussed. The field experiences with asphaltene and wax deposition and their related problems are discussed in part III. In order to predict the phenomena of asphaltene deposition one has to consider the use of the molecular thermodynamics of fluid phase equilibria and the theory of colloidal suspensions. In part IV of this report predictive approaches of the behavior of reservoir fluids and asphaltene depositions are reviewed from a fundamental point of view. This includes correlation and prediction of the effects of temperature, pressure, composition and flow characteristics of the miscible gas and crude on (i) Onset of asphaltene deposition (ii) Mechanism of asphaltene flocculation. The in situ precipitation and flocculation of asphaltene is expected to be quite different from the controlled laboratory experiments. This is primarily due to the multiphase flow through the reservoir porous media, streaming potential effects in pipes and conduits, and the interactions of the precipitates and the other in situ material presnet. In part V of the present report the conclusions are stated and the requirements for the development of successful predictive models for the asphaltene deposition and flocculation are discussed. [Pg.446]

Chemical engineers have traditionally approached kinetics studies with the goal of describing the behavior of reacting systems in terms of macroscopically observable quantities such as temperature, pressure, composition, and Reynolds number. This empirical approach has been very fruitful in that it has permitted chemical reactor technology to develop to a point that far surpasses the development of theoretical work in chemical kinetics. [Pg.1]

Chapter 12 treats situations where both physical and chemical rate processes influence the conversion rate the present chapter is concerned only with those situations where physical rate processes are unimportant. This approach permits us to focus our concern on the variables that influence intrinsic chemical reaction rates (i.e., temperature, pressure, composition, and the presence or absence of catalysts in the system). [Pg.26]

A range of different methods measures the solubility of hydrogen in metals and alloys. Manometric methods [98] and gas volumetric methods [99] have been used to determine pressure-composition isotherms at selected temperatures for a range of alloys [100-103],... [Pg.325]

Fig. 6. Pressure-composition isotherms at 300°C for MgH2 with ceramic catalyst addition. Fig. 6. Pressure-composition isotherms at 300°C for MgH2 with ceramic catalyst addition.

See other pages where Pressure-composition is mentioned: [Pg.302]    [Pg.13]    [Pg.6]    [Pg.7]    [Pg.7]    [Pg.179]    [Pg.2292]    [Pg.642]    [Pg.350]    [Pg.291]    [Pg.16]    [Pg.17]    [Pg.17]    [Pg.290]    [Pg.294]    [Pg.349]    [Pg.259]    [Pg.133]    [Pg.319]    [Pg.287]    [Pg.221]    [Pg.318]    [Pg.337]    [Pg.32]   


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