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System dispersed parameter

Method of Moments The first step in the analysis of chromatographic systems is often a characterization of the column response to sm l pulse injections of a solute under trace conditions in the Henry s law limit. For such conditions, the statistical moments of the response peak are used to characterize the chromatographic behavior. Such an approach is generally preferable to other descriptions of peak properties which are specific to Gaussian behavior, since the statisfical moments are directly correlated to eqmlibrium and dispersion parameters. Useful references are Schneider and Smith [AJChP J., 14, 762 (1968)], Suzuki and Smith [Chem. Eng. ScL, 26, 221 (1971)], and Carbonell et al. [Chem. Eng. Sci., 9, 115 (1975) 16, 221 (1978)]. [Pg.1532]

Where specialized fluctuation data are not available, estimates of horizontal spreading can be approximated from convential wind direction traces. A method suggested by Smith (2) and Singer and Smith (10) uses classificahon of the wind direction trace to determine the turbulence characteristics of the atmosphere, which are then used to infer the dispersion. Five turbulence classes are determined from inspection of the analog record of wind direction over a period of 1 h. These classes are defined in Table 19-1. The atmosphere is classified as A, B2, Bj, C, or D. At Brookhaven National Laboratory, where the system was devised, the most unstable category. A, occurs infrequently enough that insufficient information is available to estimate its dispersion parameters. For the other four classes, the equations, coefficients, and exponents for the dispersion parameters are given in Table 19-2, where the source to receptor distance x is in meters. [Pg.301]

The values of the half-widths of the components of the rotational absorption spectrum of HC1, dissolved in various noble gases, are borrowed from [291]. In order to make this example obvious, a continuous curve is drawn through the calculated points. Comparison between experimental data and calculated results demonstrates, in line with the qualitative agreement, a good numerical coincidence of the observed. /-dependence of the half-widths of the rotational lines with the theoretical one in the case of HC1 dissolved in Kr and Xe. This allows one to estimate the model parameters for these systems dispersion of the potential... [Pg.248]

Fig. 54 quantifies the relation between the yield value and a number of system-inherent parameters. The curves show that the yield value t decreases with the cube of the particle size and increases drastically with the pigment volume concentration. Since the yield value is an indication of pigment-vehicle interaction, it is also proportional to the degree of pigment dispersion [114], Interparticle attractions have received considerable theoretical and experimental treatment, and a large number of original publications and reviews are available (such as [115-117]). [Pg.105]

Parameters FT System Dispersive Liquid Crystal Tunable Filter... [Pg.429]

The communication between off-line coupled meteorological and AQ models is often a problem of underestimated importance. The variety of modelling systems previously introduced give rise to different approaches and methods implemented within interface modules. Tasks covered by interfaces are minimized in coupled systems relying on surface fluxes, turbulence and dispersion parameters (i.e. eddy... [Pg.97]

Here x and x are column vectors of the components x (t) and x (t), respectively, and A(t) is now a physical reaction matrix containing time-dependent elements. Fluorescence of kinetic transients, e. g., the relaxation profiles of monomer- or excimer fluorescence are, therefore, strictly nonexponential for which closed form, analytical solutions can be found in few cases, only. A convincing manifestation of nonexponential trapping in low-temperature, solid state p-N-VCz is a recent analysis by Bassler et al. (4, ). With the use of rate function in Equation 2, the transient ps-rise profile of the low-energy excimer E2 has been satisfactorily fitted to the numerical solution of Equation 3 with a single-fit dispersion parameter a between 0.2 and 0.8 depending on the temperature of the system. [Pg.230]

In a transition from an individual capillary to a real structured disperse system (membrane or diaphragm), one faces complications related to the actual structure of porous medium, in which the transfer of substance and electric current take place. In such systems all previously described basic relationships remain valid, but the radius and length of a single capillary are replaced with coefficients having particular dimensions, referred to as the structure parameters . In general, the determination of these structure parameters is a rather difficult task, but one may expect that in the description of electroosmotic transfer and the electric conductivity of the structured disperse systems these parameters are included in an identical way, similar to the identical dependence of IE and QE on r and /, as shown in eqs (V.32) and... [Pg.376]

Force fields for [BMIM][PF6] that explicitly treat aU hydrogens (all-atom models) were developed soon after this by Margulis et al. [14], and Morrow and Maginn [11], while Stassen and coworkers [83] published a force field for the [EMIM]+ and [BMIM]+ cations paired with tetrachloroaluminate and tetrafluoroborate anions. The force fields aU have similar functional forms, and parameters were again maiiily developed using literature force field parameters for similar compounds and ab initio calculations of single ions or ion pairs. In these and later studies, repulsion-dispersion parameters were generally adapted from those available from one of three popular force field databases (Amber [114], OPLS [118] and CHARMM [119]). For [BMIM][PF6], the added realism of the all-atom model enabled densities to be predicted vyithin 1% of the experimental value [11]. The first indications of restricted dynamics in these systems were also observed [11,14,15]. [Pg.225]

The initial and boundary conditions that apply to this equation depend on whether one is dealing with a pulse or a step stimulus and the characteristics of the system at the tracer injection and monitoring stations. At each of these points the tubular reactor is characterized as closed or open, depending on whether or not plug flow into or out of the test section is assumed. A closed boundary is one at which there is plug flow outside the test section an open boundary is one at which the same dispersion parameter characterizes the flow conditions within and adjacent to the test section. There are then four different possible sets of boundary conditions on equation (11.1.29), depending on whether a completely open or completely closed vessel, a closed-open vessel, or an open-closed vessel is assumed. Different solutions will be obtained for different boundary conditions. Fortunately, for small values of the dispersion parameter, the numerical differences between the various solutions will be small. [Pg.344]

One characteristic of the solutions for Eqs. [18-541 and [18-551 for linear isotherms is mass transfer resistances and axial dispersion both cause zone spreading that looks identical if the mass transfer parameters or axial dispersion parameters are adjusted. Thus, from an experimental result it is impossible to determine if the spreading was caused solely by mass transfer resistances, solely by axial dispersion, or by a combination of both. This property of linear systems allows us to use sinple models to predict the behavior of more complex systems. [Pg.861]

Khlebtsov et al. (1991) have theoretically and experimentally studied the dispersion effect of the refractive indices of particles and dispersion medium in the turbidity spectrum method. A new approach is put forward to estimate the optical dispersion of the components of a colloidal system and to consider it when the system s parameters are determined from the wavelength exponent. The method has been verified on PS lattices with the particle diameter from 80 to 800 nm. The elaborated version of the turbidity spectrum method can be used as a metrological test for particle sizes, not inferior to electron microscopy in accuracy. [Pg.146]

Conductive-system dispersive response may be associated with a distribution of relaxation times (DRT) at the complex resistivity level, as in the work of Moynihan, Boesch, and Laberge [1973] based on the assumption of stretched-exponential response in the time domain (Eq. (118), Section 2.1.2.7), work that led to the widely used original modulus formalism (OMF) for data fitting and analysis, hi contrast, dielectric dispersive response may be characterized by a distribution of dielectric relaxation times defined at the complex dielectric constant or permittivity level (Macdonald [1995]). Its history, summarized in the monograph of Bbttcher and Bordewijk [1978], began more than a hundred years ago. Until relatively recently, however, these two types of dispersive response were not usually distinguished, and conductive-system dispersive response was often analyzed as if it were of dielectric character, even when this was not the case. In this section, material parameters will be expressed in specific form appropriate to the level concerned. [Pg.264]


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See also in sourсe #XX -- [ Pg.33 ]




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Dispersed systems

Dispersed systems, dispersions

Dispersion parameters

Dispersive systems

System parameters

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