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Reference Composition

Reference Composition Details of test Results reported Scaling rate (mgdm d )... [Pg.1006]

Table 19.1 Composition of various buffer systems possibly eligible for combined dissolution and permeation testing. Concentrations may vary from reference to reference. Composition of FaSSIF and FeSSIF is shown as reported by Galia et al. [3] in the meantime, several publications denoted a change from potassium to sodium as the main cation [91] or others changes. Abbreviations are given in the text. [Pg.437]

Figure 9. Sketch of the double spike Zn- Zn method. The surface is constructed by drawing an infinite number of straight-lines through the point representing the spike composition (supposed to be known with no error) and each point of the mass fractionation line going through the point representing the measured mixture. One of these straightlines, which is to be determined from the calculations, is the sample-spike mixing line (stippled line). Each determination of the Zn isotope composition of a sample involves only one run for the mixture of the sample with the spike. Since all natural samples plot on the same mass fractionation line, any reference composition will adequately determine isotope composition of the sample, note that, since the instrumental bias is not linear with mass, the mass discrimination lines are curved. Figure 9. Sketch of the double spike Zn- Zn method. The surface is constructed by drawing an infinite number of straight-lines through the point representing the spike composition (supposed to be known with no error) and each point of the mass fractionation line going through the point representing the measured mixture. One of these straightlines, which is to be determined from the calculations, is the sample-spike mixing line (stippled line). Each determination of the Zn isotope composition of a sample involves only one run for the mixture of the sample with the spike. Since all natural samples plot on the same mass fractionation line, any reference composition will adequately determine isotope composition of the sample, note that, since the instrumental bias is not linear with mass, the mass discrimination lines are curved.
In this equation the reference composition (designated by the ref subscript) lies on the fractionation curve and might be, for example, the initial composition for an array of fractionated samples. All of the 5 values in the equation refer to the same standard (e.g., DSM3) but this standard need not be on the fractionation curve itself (in other words, the fractionation curves described by Equation (14) do not have to pass through the origin on a plot of 5 "Mg vs. 5 Mg). [Pg.208]

Coupons of the materials were exposed to various acid compositions and temperatures in stirred vessels. The acid compositions used in the tests reflected various average annual acid compositions likely to be encountered in the pilot-scale distillation system HNO3 - 10 to 60 wtZ H2SO4 - 0 to 60 wtZ HF - 0 to 0.2 wtZ. The coupons were suspended in six stirred vessels containing mixed acid solutions for tests at ambient temperatures. One set of coupons was placed in a round-bottomed flask containing acid with the reference composition (Case II in Table 2) and maintained at a temperature of 100 C. [Pg.317]

The X-phase is similar to the Y-phase (see Fe-Mo-S system above). With increasing temperatures the X-phase expands its compositional range5,62 and surpasses the Y-phase solid solution width. But in contrast to the Y-phase, the reference composition of the X-phase has at all temperatures a Cu Mo ratio of 1 2. [Pg.134]

A physical environment described by a reference pressure p0> reference temperature T0, and a set of reference chemical potentials [yc 0] (or alternatively reference compositions [xc Q])... [Pg.216]

For a reliable choice of pairs hydrides, and also for designing hydrides it would be desirable to have universal P-C-T dependence for hydrides. In the literature there is semi-empirical equation for equilibrium P-C-T of dependences [4] where the data are generalized with use of function of free energy RTLn(P/PXI) (where P - scale of pressure for reference composition XT, for example, taken in the middle a plateau of an isotherm of P-C). The given function reduces isotherms for various temperatures on one curve. Thus branches of isotherms of absorption and desorption can agree with a suitable choice of reference pressure PXI. For... [Pg.385]

Here, p°° and p°° are standard chemical potentials of reaction groups i and j of the reference composition p° and p° the same of the groups of the inspected composition and Xy and Xji are dimensionless correlation coef ficients. Coefficients Xy usually fall in the range between 0.1 and 0.5. [Pg.222]

Even with propylene feed, a high isobutane-to-olefin ratio influences the product toward predominantly Cg hydrocarbons which have the highest octane number and also Improves yields. Thus, both alkylate quality and yield are found to improve with increasing ratio and olefin dilution. In Table IX, detailed propylene-isobutane alkylate composition data are shown, where the volume ratio was increased from 4.6 to 126. For quick reference, composition data are summarized in Table IV. [Pg.44]

We used the compositions determined by this study to obtain the reference composition for each of the two samples, and calculated the errors in determining each amino acid using this composition. The pre-hydrolysate was more accurately analyzed than the protein, which was hydrolyzed by the participants. The overall average errors were 6.52% (Table ni) and 8.36% (Table II), respectively... [Pg.188]

Here /, has been written as a function of the m concentrations, the temperature, and pressure. It should also be remembered that a reference composition, c,o, is implicit infc, it is sometimes, but not... [Pg.37]

We have seen in Chapter 3 that if Cj is the concentration of the chemical species A,- which is taking part in the reactionX i a.Ai = 0, then Ci = c,o + a.r , where c, is the concentration in some reference state and c the extent of reaction. The rate of reaction, r c,T), is defined as the time derivative of c and is a function of c and the temperature T. (We are assuming that the pressure and reference composition are constant.) The sequence of R reactors is numbered from the last to the first (see Fig. 5.1) and a suffix r denotes values... [Pg.64]

There are thus in general (2n + 3) parameters, which fall into groups as follows p, an exponent related only to the activation energy k related to the kinetic constants and Co ju, related to the initial or reference composition related to the order of the reaction and r, r related to the bounds on the temperature. The equations governing the system when r < r < r are... [Pg.77]

Two compositions c] and c , i = 1,. . . n, will be called alien if they cannot both arise from the same reference composition Cio by reaction to a certain extent. Thus two compositions are alien if (cj — c i)/ai is not independent of i for a single reaction, and a more complicated relation holds for simultaneous reactions. We will consider the case where the source of supply for the cold shot is of an alien composition. This sometimes occurs in practice, as when air is used as the cold shot in the oxidation of sulfur dioxide. [Pg.127]

Let c,o be the reference composition of the main supply of process stream and 7, that of the cold shot supply. Suppose a quantity of reactants of composition c, = c,o + afi is mixed with cold shot in the proportions X (T— X). The resulting composition is... [Pg.127]

This has the same reference composition as (3) but an extent of reaction /xXc + fxc. It appears therefore that the reference composition changes only with the mixing. The extent changes only with the proportion of mixing that occurs after a ven amount of reaction. [Pg.128]

The constant A is used to render the time dimensionless. In case the kinetic constants /3, are fixed and we consider only one reference composition, there are only two parameters p and k and these are separated in the sense that p is associated with the integral F whilst K is associated with the temperature policy. [Pg.136]

Millero, F. J., Feistel, R., Wright, D. G., McDougall, T. J., 2008. The Composition of Standard Seawater and the Definition of the Reference-Composition Salinity Scale. Deep-Sea Research, I, 55, 50-72. [Pg.335]

TABLE 20.1 The Definition of Reference Composition, Providing the Cnrrently Best Estimate of the Absolute Salinity of Standard Seawater, Equation 20.1. X-Mole Fractions, Z-Valences, W-Mass Fractions (Millero et al., 2008). [Pg.628]

Another item of the forthcoming recommendation by the WG127 concerns a new salinity definition called Reference-Composition Salinity, bringing this fundamental oceanographic measure back into the interdisciplinary scientific and engineering family of the SI system of units (BIPM, 2006 Millero et al., 2008). The chemical Reference Composition is given in Table 20.1. On the basis of this definition, the recommended conversion formula between Absolute Salinity, S, and Practical Sahnity, S, of standard seawater is given by... [Pg.628]

Of particular interest for the winter convection and the formation of the winter water layer are the temperatures of maximum density and the freezing points. Reported in Table 20.3 are the freezing points, tf, and the temperatures of maximum density, t D, for brackish seawater of Reference Composition (Millero et al., 2008) with absolute salinity, 5a, between 0 and 25 g/kg, computed from the lAPWS formulations for water (lAPWS, 1996), ice (lAPWS, 2006), and the saline Gibbs function (Feistel, 2007). [Pg.629]


See other pages where Reference Composition is mentioned: [Pg.215]    [Pg.673]    [Pg.208]    [Pg.221]    [Pg.54]    [Pg.229]    [Pg.127]    [Pg.217]    [Pg.236]    [Pg.296]    [Pg.597]    [Pg.88]    [Pg.387]    [Pg.1196]    [Pg.1198]    [Pg.1201]    [Pg.4771]    [Pg.40]    [Pg.44]    [Pg.76]    [Pg.127]    [Pg.136]    [Pg.180]    [Pg.138]    [Pg.17]   
See also in sourсe #XX -- [ Pg.628 , Pg.629 ]




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