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It is not uncommon to encounter emulsions, foams, and suspensions, both in nature and in industry, that contain polymers. If the polymer concentration is high enough, and the dispersed species concentration low enough, the overall viscosity may be better described by the contribution from the polymer solution than that from the dispersed species. One commonly employed equation for describing the viscosity of polymer solutions is the Carreau equation, [Pg.192]

For an isothermal vapor-liquid flash, T is icnown and Equation (7-14) is used only to find Q after the other equations have... [Pg.114]

The multilayer isotherms illustrated thus far have all been of a continuous appearance—it was such isotherms that the BET, FHH, and other equations treated. About 30 years ago, however, multilayer adsorption on smooth sur-... [Pg.639]

In reeent years global phase diagrams have been ealeulated for other equations of state, not only van der Waals-like ones, but others with eomplex temperature dependenees. Some of these have managed to find type VI regions in the overall diagram. Some of the reeent work was brought together at a 1999 eonferenee [4]. [Pg.626]

Equation (26) is a set of partial first-order differential equations. Each component of the Curl forms an equation and this equation may or may not be coupled to the other equations. In general, the number of equations is equal to the number of components of the Curl equations. At this stage, to solve this set of equation in its most general case seems to be a fomiidable task. [Pg.692]

The degree of the least equation, k, is called the rank of the matrix A. The degree k is never greater than n for the least equation (although there are other equations satisfied by A for which k > n). If A = n, the size of a square matrix, the inverse A exists. If the matrix is not square or k < n, then A has no inverse. [Pg.37]

Linear independence implies that no equation in the set can be obtained by multiplying any other equation in the set by a constant. The n x n matrix populated by n elements Gy... [Pg.45]

The Klopm an-Salem equation partitions contributions to the interaction energy of two molecules into two teams, as they approach each other (equation 29). [Pg.139]

Sorption Modeling. Pesticide sorption is characterized by describing sorption isotherms using the Freundhch equation, S = Kj, where S is the pesticide sorbed concentration, C is the pesticide solution concentration after equdibration, and fy and N are constants. Although other equations have been used, the Freundhch has satisfactodly described experimental sorption results for a wide range of pesticides in a variety of sods. The value of N is usually <1 and between 0.75 and 0.95, which indicates that pesticides are proportionally more sorbed at low solution concentration than at high solution concentration. [Pg.221]

This fundamental property relation is the basis for development of aU. other equations relating the properties of PTTsystems. [Pg.487]

There are other equations for other illuminants and other observers (3) and also various modifications for special conditions (31). [Pg.415]

Corresponding states have been used in other equations. For example, the Peng-Robinson equation is a modified RedHch-Kwong equation formulated to better correlate vapor—Hquid equiHbrium (VLE) vapor pressure data. This equation, however, is not useful in reduced form because it is specifically designed to calculate accurate pressure data. Reduced equations generally presuppose knowledge of the pressure. [Pg.240]

Using the other equations for U, H, A, or S gives the other possibihties. Type III ( 15 possibihties plus reciprocals)... [Pg.445]

Equation (4-8) is the fundamental property relation for singlephase PVT systems, from which all other equations connecting properties of such systems are derived. The quantity is called the chemical potential of ecies i, and it plays a vital role in the thermodynamics of phase ana chemical equilibria. [Pg.515]

Combine these reac tion equations so as to ehminate from the set all elements not present as elements in the system. A systematic procedure is to select one equation and combine it with each of the other equations of the set so as to ehminate a particular element. This usually reduces the set by one equation for each element ehminated, though two or more elements may be simultaneously eliminated. [Pg.535]

Evaluation of 9 is usually by Eq. (4-196), based on the two-term virial equation of state, but other equations, such as Eq. (4-200), are also applicable. The activity coefficient Jj is evaluated by Eq. (4-119), which refates In Jj to G /RT as a partial proper. Thus, what is required for the hquid phase is a relation between G /BT and composition. Equations in common use for this purpose have already been described. [Pg.535]

Details of the derivations of these and some other equations are presented by Yang and Hougen (Chem. Eng. Prog., 46, 146 [1950]),... [Pg.692]

Other equations in general use include the Gates-Gaudin-Schumann [Schumann, Am. Inst. Min. Metall. Pet. Eng., Tech. Paper 1189, Min. Tech. (1940)] ... [Pg.1823]

This equation is not particularly useful in practice, since it is difficult to quantify the relationship between concentration and ac tivity. The Floiy-Huggins theory does not work well with the cross-linked semi-ciystaUine polymers that comprise an important class of pervaporation membranes. Neel (in Noble and Stern, op. cit., pp. 169-176) reviews modifications of the Stefan-Maxwell approach and other equations of state appropriate for the process. [Pg.2054]

The Golay equation [9] for open tubular columns has been discussed in the previous chapter. It differs from the other equations by the absence of a multi-path term that can only be present in packed columns. The Golay equation can also be used to examine the dispersion that takes place in connecting tubes, detector cells and other sources of extra-column dispersion. Extra-column dispersion will be considered in another chapter but the use of the Golay equation for this purpose will be briefly considered here. Reiterating the Golay equation from the previous chapter. [Pg.266]

Other equations describing the wind profile are available from ASHRAE and from Sherman and Grimsrud. ... [Pg.575]

Panagiotopoulos et al. [16] studied only a few ideal LJ mixtures, since their main objective was only to demonstrate the accuracy of the method. Murad et al. [17] have recently studied a wide range of ideal and nonideal LJ mixtures, and compared results obtained for osmotic pressure with the van t Hoff [17a] and other equations. Results for a wide range of other properties such as solvent exchange, chemical potentials and activity coefficients [18] were compared with the van der Waals 1 (vdWl) fluid approximation [19]. The vdWl theory replaces the mixture by one fictitious pure liquid with judiciously chosen potential parameters. It is defined for potentials with only two parameters, see Ref. 19. A summary of their most important conclusions include ... [Pg.781]

Equation (3-150) and other equations of the same functional form can be placed in three linear plotting forms, of which the double-reciprocal form is shown as Eq. (3-152). Find the other two linear plotting forms. [Pg.131]

Equation (6-19) was said to provide a fit as good as or better than those with other equations. The parameters were evaluated by fixing C and carrying out a linear least-squares regression of In k on T C was then altered and the procedure was repeated. The residual sum of squares was taken as a criterion of best fit. [Pg.253]

Equation (7-29) is linear in the parameters and can be regarded as a multiple LEER. Many other equations of this form have been proposed. [Pg.323]

The iiitemil energy and entlialpy in Eqs. (4.5.2) uid (4.5.3), as well as in tlie other equations in tliis discussion, may be on a mass or a mole basis, or tliey may represent the total internal energy and entlialpy of tlie entire system. Most industrial facilities operate in a steady-state flow mode. If no significant mechanical or shaft work is added or withdrawn from tlie system, Eq. (4.5.3) reduces to... [Pg.121]

Other equations are presented in Ref. [27] to represent the dust nomographs of Figures 7-65D through 65H. Reference conversions ... [Pg.513]

Ward and Sommerfeld [130] present an equation based on the curves shown in Figure 9-21C, D and referenced to Eckert [125] and Leva [43] for calculating the gas and liquid flooding rates. There have been numerous other equations targeted for this pmpose, but many are too awkward for easy general use. The proposed equations have been tested by the authors. [Pg.310]

Many other equations could be written for this system, for example,... [Pg.327]

To what extent are these or other equations, which were suggested for the description of thet versus cp dependence general or universal ... [Pg.84]

It is evident that the equation for Ref. 13 has broken down completely for CO hydrogenation. The other equations (II, 14) for CO hydrogenation gave correlations similar to those obtained by the simple kinetics. These equations are all, however, of relatively simple form. They use low activation energies and in general show an activity dependence on the square root of the pressure, similar to that of the simple kinetics. [Pg.76]

Many other equations of state besides van der Waals lead to laws of corresponding states, although naturally these will not be of the form (1). [Pg.229]

Other equations of state can be used to calculate virial equation6 is given by... [Pg.252]

Equations of state, such as the virial equation, demonstrate that o remains finite as p— 0. See Appendix 3 for a discussion of the virial and other equations of state. [Pg.252]

The fugacity coefficient can be calculated from other equations of state such as the van der Waals, Redlick-Kwong, Peng-Robinson, and Soave,d but the calculation is complicated, since these equations are cubic in volume, and therefore they cannot be solved explicitly for Vm, as is needed to apply equation (6.12). Klotz and Rosenburg4 have shown a way to get around this problem by eliminating p from equation (6.12) and integrating over volume, but the process is not easy. For the van der Waals equation, they end up with the relationship... [Pg.256]

See other pages where Other Equations is mentioned: [Pg.115]    [Pg.964]    [Pg.13]    [Pg.128]    [Pg.515]    [Pg.359]    [Pg.600]    [Pg.1208]    [Pg.1255]    [Pg.336]    [Pg.284]    [Pg.163]    [Pg.341]    [Pg.134]    [Pg.73]    [Pg.329]    [Pg.114]   


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Applying the Clapeyron Equation to Other Kinds of Equilibrium

Equations of state other

Equations other equipment (Table

Other Empirical Equations

Other Fundamental Equations

Other Integral Constitutive Equations

Other Isotherm Equations

Other Two-parameter Equations

Other flow equations

Other methods depending directly on the fundamental equation

Some Other Examples of Balancing Equations

Some other formulations of the energy equation

The Antoine Equation and Other Data-Fitting Equations

Van der Waals and Other Model Equations of State

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