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Mixed gases heat capacity

As mentioned before, Approach A (also called supercritical compounds can be handled easily and that besides the phase equilibrium behavior various other properties such as densities, enthalpies including enthalpies of vaporization, heat capacities and a large number of other important thermodynamic properties can be calculated via residual functions for the pure compounds and their mbctures. For the calculation besides the critical data and the acentric factor for the equation of state and reliable mixing rules, only the ideal gas heat capacities of the pure compounds as a function of temperature are additionally required. A perfect equation of state with perfect mixing rules would provide perfect results. This is the reason why after the development of the van der Waals equation of state in 1873 an enormous number of different equations of state have been suggested. [Pg.235]

Mixed or activity coefficient Molecular Weight (MW) Ideal Gas Heat Capacity (CPjq) Vapor Pressure (Pvap) Heat of Vaporization (AHvap) Liquid Heat Capacity (CP,jq) Liquid Density (pj Solubility Parameter (d) Yes, however, best with heavy components that the EOS approach cannot deal with... [Pg.44]

Solution calorimetry covers the measurement of the energy changes that occur when a compound or a mixture (solid, liquid or gas) is mixed, dissolved or adsorbed in a solvent or a solution. In addition it includes the measurement of the heat capacity of the resultant solution. Solution calorimeters are usually subdivided by the method in which the components are mixed, namely, batch, titration and flow. [Pg.1910]

Because of its small size and portabiHty, the hot-wire anemometer is ideally suited to measure gas velocities either continuously or on a troubleshooting basis in systems where excess pressure drop cannot be tolerated. Furnaces, smokestacks, electrostatic precipitators, and air ducts are typical areas of appHcation. Its fast response to velocity or temperature fluctuations in the surrounding gas makes it particularly useful in studying the turbulence characteristics and rapidity of mixing in gas streams. The constant current mode of operation has a wide frequency response and relatively lower noise level, provided a sufficiently small wire can be used. Where a more mgged wire is required, the constant temperature mode is employed because of its insensitivity to sensor heat capacity. In Hquids, hot-film sensors are employed instead of wires. The sensor consists of a thin metallic film mounted on the surface of a thermally and electrically insulated probe. [Pg.110]

The use of mixed gases is designed to equalize the heat capacities of the two counterflow gas streams and thereby make the exchange process much more efficient. However, the expanded fluid is a mixture of liquid and gas hence a liquid-vapour separator is needed to allow the expanding liquid to precool the vapour. Figure 5.13 shows the cycle as modified by MMR Technologies [53]... [Pg.140]

Assuming plug flow of the gas and complete mixing of the solids, calculate the coefficient for heat transfer between the particles and the gas. The specific heat capacity of air is 0.85 kJ/kg K. [Pg.62]

Solids in Mixed Flow, The fluidized bed [Fig. 26.1(d)] is the best example of a reactor with mixed flow of solids. The gas flow in such reactors is difficult to characterize and often is worse than mixed flow. Because of the high heat capacity of the solids, isothermal conditions can frequently be assumed in such operations. [Pg.589]

For miscible blend phases, these parameters need to be described as a function of the blend composition. In a first approach to describe the behavior of the present PPE/PS and SAN/PMMA phases, these phases will be regarded as ideal, homogeneously mixed blends. It appears reasonable to assume that the heat capacity, the molar mass of the repeat unit, as well as the weight content of carbon dioxide scale linearly with the weight content of the respective blend phase. Moreover, a constant value of the lattice coordination number for PPE/PS and for SAN/PMMA can be anticipated. Thus, the glass transition temperature of the gas-saturated PPE/SAN/SBM blend can be predicted as a function of the blend composition (Fig. 17). Obviously, both the compatibilization by SBM triblock terpolymers and the plasticizing effect of the absorbed carbon dioxide help to reduce the difference in glass transition temperature between PPE and SAN. [Pg.222]

A mixed gas of 60-75 percent C02 derived from mixing the 40 percent C02 from the kilns and the 90 percent C02 from the calcinations of bicarbonate, is fed to the bottom of these crystallizing units. Absorption of C02 in the highly alkaline ammoniated brine results in crystallization of crude sodium bicarbonate. Because of the heat evolved in the absorption and neutralization of the carbonic acid gas and from crystallization of the sodium bicarbonate, the temperature of the liquor in the column rises from 38°C to a maximum of about 62-64°C. In normal operation, the temperature of the discharge slurry is maintained at about 27°C by automatic adjustment of the water flow through the cooling tubes. A tower such as that shown in Fig. 26.2 has a capacity for producing 50 tons per day of finished soda. [Pg.1187]

The fluidized bed characteristics of high solids heat capacity, large interfacial heat transfer area, and good solids mixing allow the assumptions of thermal equilibrium between the solids and the gas, uniform bed temperature and negligible heat capacitance of the gas. An additional assumption required to use equation (9) is that the reactions do not change the gas volume. [Pg.57]

The products of a detonation or burning reaction are mixtures of different reaction products, usually gases. It would be very inconvenient to treat each one separately. The mixed gases can be treated as a single gas with an average heat capacity value. The heat capacity of the mixture is equal to the sum of the products of the mole fraction of each gas component times its heat capacity. [Pg.103]

Heat and mass transfer constitute fundamentally important transport properties for design of a fluidized catalyst bed. Intense mixing of emulsion phase with a large heat capacity results in uniform temperature at a level determined by the balance between the rates of heat generation from reaction and heat removal through wall heat transfer, and by the heat capacity of feed gas. However, thermal stability of the dilute phase depends also on the heat-diffusive power of the phase (Section IX). The mechanism by which a reactant gas is transferred from the bubble phase to the emulsion phase is part of the basic information needed to formulate the design equation for the bed (Sections VII-IX). These properties are closely related to the flow behavior of the bed (Sections II-V) and to the bubble dynamics. [Pg.360]

It is instructive to compare gas-liquid reactors (from all the classes) on the basis of capacity, turndown ratio (L/G), liquid-phase axial mixing, gas-side pressure drop, mass transfer coefficient, effective interfacial area, heat transfer coefficient, and the number of theoretical stages. Table 11.26 presents such a comparison using ratings 1 to 5 (poor to excellent). This table should be useful to design engineers. [Pg.849]

The standard state for a pure liquid or solid is taken to be the substance in that state of aggregation at a pressure of 1 bar. This same standard state is also used for liquid mixtures of those components that exist as a liquid at the conditions of the mixture. Such substances are sometimes referred to as liquids that may act as a solvent. For substances that exist only as a solid or a gas in the pure component state at the temperature of the mixture, sometimes referred to as substances that can act only as a solute, the situation is more complicated, and standard states based on Henry s law may be used. In this case the pressure is again fixed at 1 bar, and thermal properties such as the standard-state enthalpy and heat capacity are based on the properties of the substance in the solvent at infinite dilution, but the standard-state Gibbs energy and entropy are based on a hypothetical state.of unit concentration (either unit molality or unit mole fraction, depending on the form of Henry s law used), with the standard-state fugacity at these conditions extrapolated from infinite-dilution behavior in the solvent, as shown in Fig. 9.1-3a and b. Therefore just as for a gas where the ideal gas state at 1 bar is a hypothetical state, the standard state of a substance that can only behave as a solute is a hypothetical state. However, one important characteristic of the solute standard state is that the properties depend strongly upon the solvent. used. Therefore, the standard-state properties are a function of the temperature, the solute, and the solvent. This can lead to difficulties when a mixed solvent is used. [Pg.462]

In slurry systems, similar to fluidized beds, the overall rate of chemical transformation is governed by a series of reaction and mass-transfer steps that proceed simultaneously. Thus, we have mass transfer from the bubble phase to the gas-liquid interface, transport of the reactant into the bulk liquid and then to the catalyst, possible diffusion within the catalyst pore structure, adsorption and finally reaction. Then all of this goes the other way for product. Similar steps are to be considered for heat transfer, but because of small particle sizes and the heat capacity of the liquid phase, significant temperature gradients are not often encountered in slurry reactors. The most important factors in analysis and design are fluid holdups, interfacial area, bubble and catalyst particle sizes and size distribution, and the state of mixing of the liquid phase. ... [Pg.593]

Loss of bearing capacity Water -content -flow Transport Mixing Reaction Displacement gas Heat Transfw Advection Dispersion... [Pg.303]

The findings from singularity analysis of the one-stage column will be checked for their relevance for the nonlinear behavior of an industrial size RD column by means of numerical bifurcation analysis using DIVA [53, 63]. The model used is of moderate complexity. The major assumptions are constant liquid holdup on every tray negligible vapor holdup, constant heat capacities and heats of vaporization of all the species, ideal gas phase, almost ideal liquid phase, perfect mixing on... [Pg.251]


See other pages where Mixed gases heat capacity is mentioned: [Pg.180]    [Pg.783]    [Pg.554]    [Pg.143]    [Pg.78]    [Pg.349]    [Pg.345]    [Pg.499]    [Pg.448]    [Pg.298]    [Pg.345]    [Pg.414]    [Pg.427]    [Pg.345]    [Pg.128]    [Pg.53]    [Pg.880]    [Pg.30]    [Pg.473]    [Pg.724]    [Pg.565]    [Pg.20]    [Pg.409]   
See also in sourсe #XX -- [ Pg.1541 , Pg.1542 ]




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