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Correlation Forms

In general, STR correlations lack the ability to account for reactor variations and the specific hydrodynamic state however, they can be used as an estimate if the [Pg.106]

A simple approach for finding an appropriate gas-liquid mass transfer correlation is to break ki a down into its components (a and l) and And separate correlations for each, after which those components would be combined to generate a k a correlation. It is very convenient to start with the interfacial area since an applicable theoretical correlation is readily available (Figueiredo and Calderbank, 1979) [Pg.107]

an assumption is made on the mass transfer model, and the two terms are combined. If a film model is used, is assumed to be inversely proportional to d. Therefore, [Pg.107]

TABLE 6.1 Gas Holdup Correlations for Stirred-Tank Reactors [Pg.108]

Researchers C a h Uq Range (mm/s) PqIV Range (W/m ) Gas Liquid Impeller Configuration 77 (m) r(m) [Pg.108]


The actual residence time of a reactor is measured by employing residence time distribution (RTD) experiments utilizing tracing techniques. Furthermore, several correlation forms estimating the fluid holdup can be found in the related literature. [Pg.93]

All superposition approximations mentioned above are based on the idea of multiplicative expansion, when m-reactant (m-point) distribution functions prn(, , m), with arguments being the generalised coordinates, are expressed through the correlation forms a(m) ... [Pg.124]

An alternative way to study many-particle effects is based on the correlation forms in the additive expansion [76]... [Pg.125]

Unfortunately, this expansion cannot be used as a basis for the development of approximate methods since - unlike the superposition approximation -in the case of considerable spatial correlation, neglect of the forms b(m m > mo leads to the correlation functions not satisfying the proper boundary conditions and increase of mo does not lead to the convergence of results. A comparison of the two kinds of expansion of the many-particle distribution function demonstrates that the superposition approximation even for small mo corresponds to the choice in the additive expansion of b 0 with any m. Therefore, in terms of the latter expansion the many-particle correlation forms are not neglected in the superposition approximations but are no longer independent. [Pg.126]

The approximations of the superposition-type like equation (2.3.54), are used in those problems of theoreticals physics when other-kind expansions (e.g., in powers of a small parameter) cannot be employed. First of all, we mean physics of phase transitions and critical phenomena [4, 13-15] where there are no small parameters at all. Neglect of the higher correlation forms a(ml in (2.3.54) introduces into solution errors which cannot be, in fact, estimated within the framework of the method used. That is, accuracy of the superposition-like approximations could be obtained by a comparison with either simplest explicitly solvable models (like the Ising model in the theory of phase transitions) or with results of direct computer simulations. Note, first of all, several distinctive features of the superposition approximations. [Pg.253]

The heat and mass transfer properties can be represented by heat and mass transfer coefficients, which are commonly given in empirical or semiempirical correlation form. The transfer coefficient is defined in terms of flow models under specific flow conditions and geometric arrangements of the flow system. Thus, when applying the correlations, it is necessary to employ the same flow model to describe the heat and mass transfer coefficients for conditions comparable to those where the correlations were obtained. An accurate characterization of the heat and mass transfer can be made only when the hydrodynamics and underlying mechanism of the transport processes are well understood. [Pg.499]

Pm with any m could be expressed through pm, m mo and we thus arrive at the superposition approximations. It is assumed that the correlation forms are small as compared to the but no distinctive small... [Pg.125]

Based on the above assumptions, correlations were developed first for the intercepts K, K ) and slopes ( , n") of log cu-log G and log tu-log G" data The correlation form that was successful was again the lower bound form of Takayanagi model (Ross-Murphy, 1984) ... [Pg.243]

Thus the development of the lowest epiphreatic cave level may have been contemporaneous with or pre-date the sediment deposition. This indicates that even the lowest cave level (and the river terrace with which it is correlated) formed in the mid-Pleistocene, or earlier. The sea level and climatic fluctuations of the late Pleistocene, responsible for the bulk of Northern Hemisphere karst geomorphology, have left little discernible trace in the Buchan area (Webb et al., 1992). [Pg.65]

All packing correlation methods for hydraulics have systemic limitations. These limits arise from the underlying correlation forms and the difficulty in data interpretation. Table 9 lists applicability ranges for Fig. 7. Strigle and Kister and Gill both have excellent discussions of the limitations of the method shown. In summary, the limitations are ... [Pg.737]

One possible approach to validate the mixing hypothesis is to show all samples together, distinguished by facies, on a 6 0 vs. 6 C cross-plot. If mixing of the initial formation waters really occurred, the expected pattern is that 6 0 vs. 6 C values of clean, well-connected sandstones would correlate, forming a trend which joins the marine and freshwater end-members represented by the calcites of isolated sandstone bodies. [Pg.157]

The value of r is calculated for all combinations of variable pairs in Po Correlation as shown in Table 2. The correlation in Table 2 shows only the correlation of pairs while more complex correlation formed by combined ranking of several variables will be investigated in the following. [Pg.264]

With these equations, the corresponding-states form pr(< >, Pr) is complete. This correlation form yields an average error for the predicted density of 0.85% on the vapor side and 0.37% on the liquid side for the substances shown in Table II. Much of this increased error stems from the data for perfluoropropane and n-decane. [Pg.378]

The ridge regression procedure modifies the least-squares regression equation by introducing a constant (c) where c > 0. Generally, c is 0 < c < 1. The population ridge regression equation, then, is in correlation form... [Pg.223]

To employ the ridge regression, first (Step 1), the values are transformed to correlation form. Correlation for the y, value is... [Pg.224]

The Xi values for each predictor variable are next transformed to correlation form using... [Pg.224]

Note This correlation form and the correlation form in Table 6.2 should be identical. They differ here because Table 6.2 was done in an autoselection of MiniTab and Table 6.8 was done via manual matrix manipulation using MiniTab. [Pg.227]

The Y correlation form matrix must then be correlated with each x, variable to form an matrix. The easiest way to do this is by computing the matrix, X Y = Vyx (Table 6.9). The next step (Step 2) is to generate sets of b data for the various c values chosen using the equation, V = + ciy Tyj, where... [Pg.227]

Note k is the number of predictor b1 variables, less bo which equals 6 b through Zjg) in our example. MSe is the mean square error, of the full regression on the correlation form of the x, and y values, when the ridge regression computed sets c = 0. That is... [Pg.235]

In Step 7, we convert the correlation form estimate back to the original scale by first finding y, Sy, x, and in the original scale, from Table 6.1A (Table 6.15). [Pg.238]

The ridge regression analysis can be extremely useful with regressions that have correlated x, predictor values. When the data are in correlation form, it is useful to mn a variety of other tests, such as ANOVA, for the model to be sure, it is adequate. In matrix form, the computations are... [Pg.240]


See other pages where Correlation Forms is mentioned: [Pg.233]    [Pg.226]    [Pg.46]    [Pg.124]    [Pg.125]    [Pg.241]    [Pg.233]    [Pg.10]    [Pg.596]    [Pg.143]    [Pg.237]    [Pg.124]    [Pg.241]    [Pg.461]    [Pg.166]    [Pg.163]    [Pg.233]    [Pg.217]    [Pg.224]    [Pg.225]    [Pg.228]    [Pg.237]    [Pg.238]    [Pg.238]    [Pg.240]   


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B — Time-Correlation Functional Form for the Relaxation Modulus

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