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Relationship between measured and

Figure 2.11 Crystallographic data collection, showing reflections measured at one particular crystal orientation (solid, on film) and those that could be measured at other orientations (hollow, within the sphere but not on the film). The relationship between measured and unmeasured reflections is more complex than shown here (see Chapter 4). Figure 2.11 Crystallographic data collection, showing reflections measured at one particular crystal orientation (solid, on film) and those that could be measured at other orientations (hollow, within the sphere but not on the film). The relationship between measured and unmeasured reflections is more complex than shown here (see Chapter 4).
The major focus of the conceptual model (Figure 2) is the development of a series of working hypotheses regarding how the stressor might affect ecological components of the natural environment (NRC, 1986). The conceptual model also includes descriptions of the ecosystem potentially at risk and the relationship between measurement and assessment endpoints. [Pg.442]

Linearity refers to the relationship between measured and expected values over the analytical measurement range. Linearity may be considered in relation to actual or relative analyte concentrations. In the latter case, a dilution series of a sample may be studied. This is often carried out for immunoassays, in which case it is investigated whether the measured concentration declines as expected according to the dilution factor. Dilution is usually carried out with the appropriate sample matrix (e.g., human serum [individual or pooled serum]). [Pg.359]

They calculated species distributions for each sample and then computed the Nernst Eh for the redox couples in the analysis. Their results show that the redox couples generally failed to achieve equilibrium with each other, varying per sample by as much as 1000 mV. In addition, they could demonstrate little relationship between measured and Nernst Eh values. Similarly, Criaud et al. (1989) computed discordant Nernst Eh values for low-temperature geothermal fluids from the Paris basin. [Pg.101]

The relationship between measured and reference values is given as the following equation ... [Pg.176]

Figure 93.6. Relationship between measured and near infrared predicted values of log SCC for the independent test set of samples. Figure 93.6. Relationship between measured and near infrared predicted values of log SCC for the independent test set of samples.
Find and discuss for the DSC shown in Fig. 4.6 a relationship between measured and actual temperature differences. What is the sample temperature lag from the recorded average temperature iiX/K = 1000 and the absolute, measured temperature difference is 0.007 K ... [Pg.210]

As seen in other chapters, the Ogston sieving model also does not describe sedimentation or diffusion through polymer solutions (cross-linked gels are a separate question not considered here), so its invocation in electrophoresis seems problematic. Conclusions about transport mechanics, drawn from relationships between measurements and a hypothesized Ogston model, are therefore subject to reservations. [Pg.63]

The process is designed from a knowledge of physical concentrations, whereas aqueous effluent treatment systems are designed from a knowledge of BOD and COD. Thus we need to somehow establish the relationship between BOD, COD, and the concentration of waste streams leaving the process. Without measurements, relationships can only be established approximately. The relationship between BOD and COD is not easy to establish, since different materials will oxidize at different rates. To compound the problem, many wastes contain complex mixtures of oxidizable materials, perhaps together with chemicals that inhibit the oxidation reactions. [Pg.309]

The flow can be radial, that is, in or out through a hole in the center of one of the plates [75] the relationship between E and f (Eq. V-46) is independent of geometry. As an example, a streaming potential of 8 mV was measured for 2-cm-radius mica disks (one with a 3-mm exit hole) under an applied pressure of 20 cm H2 on QT M KCl at 21°C [75]. The i potentials of mica measured from the streaming potential correspond well to those obtained from force balance measurements (see Section V-6 and Chapter VI) for some univalent electrolytes however, important discrepancies arise for some monovalent and all multivalent ions. The streaming potential results generally support a single-site dissociation model for mica with Oo, Uff, and at defined by the surface site equilibrium [76]. [Pg.188]

Now the relationship between v and A is given by the size distribution curve the value of A merely represents the lengths of the particles measured in terms of a particular, arbitrary, unit. Thus, if the size distribution curve remains of exactly the same shape during the grinding process, the values of... [Pg.31]

A second complication in measuring pH results from uncertainties in the relationship between potential and activity. For a glass membrane electrode, the cell potential, Ex, for a solution of unknown pH is given as... [Pg.491]

Relationship Between Measurement Error in Potential and Relative Error in Concentration... [Pg.495]

Values of Vmax and Km for reactions obeying the mechanism shown in reaction 13.15 can be determined using equation 13.18 by measuring the rate of reaction as a function of the substrate s concentration. The curved nature of the relationship between rate and the concentration of substrate (see Figure 13.10), however, is inconvenient for this purpose. Equation 13.18 can be rewritten in a linear form by taking its reciprocal... [Pg.638]

The treatment of heat capacity in physical chemistry provides an excellent and familiar example of the relationship between pure and statistical thermodynamics. Heat capacity is defined experimentally and is measured by determining the heat required to change the temperature of a sample in, say,... [Pg.506]

To use GPC for molecular weight determination, we must measure the volume of solvent that passes through the column before a polymer of particular molecular weight is eluted. This quantity is called the retention volume Vj. Figure 9.14 shows schematically the relationship between M and Vj it is an... [Pg.643]

Noise reduction (AIR) is the difference in the average sound pressure level between the source room and the receiving room. When the receiving room is relatively reverberant and the measurements are made in the reverberant fields of the two rooms the relationship between TL and AIR is as follows, where S is the surface area of the sound barrier between the two rooms and is the amount of sound absorption in the receiving room (7). [Pg.315]

Effect of Shear. Concentrated aqueous solutions of poly(ethylene oxide) are pseudoplastic. The degree of pseudoplasticity increases as the molecular weight increases. Therefore, the viscosity of a given aqueous solution is a function of the shear rate used for the measurement. This relationship between viscosity and shear rate for solutions of various molecular weight poly(ethylene oxide) resins is presented in Figure 8. [Pg.341]

Evidence of the appHcation of computers and expert systems to instmmental data interpretation is found in the new discipline of chemometrics (qv) where the relationship between data and information sought is explored as a problem of mathematics and statistics (7—10). One of the most useful insights provided by chemometrics is the realization that a cluster of measurements of quantities only remotely related to the actual information sought can be used in combination to determine the information desired by inference. Thus, for example, a combination of viscosity, boiling point, and specific gravity data can be used to a characterize the chemical composition of a mixture of solvents (11). The complexity of such a procedure is accommodated by performing a multivariate data analysis. [Pg.394]

Density. Measurement of density is widely used in the sugar industry to determine the sugar concentration of symps, Hquors, juices, and molasses. The instmment used is called a hydrometer or a spindle. When it is graduated in sucrose concentration (percent sucrose by weight), it is called a Brix hydrometer or a Brix spindle. Brix is defined as the percent of dry substance by hydrometry, using an instmment or table caUbrated in terms of percent sucrose by weight in water solution. Hydrometers are also graduated in °BaumH, stiU in use in some industries. The relationship between °BaumH and density, ing/cm, is °Baumn Baum e = 145(1 — 1/d). [Pg.10]

One measure of impact resistance is the laminate s mean break height (MBH) (102). In the standard test, there is a 50% probabiHty that a five-pound (2.27-kg) ball will not fall through a laminate if the ball is dropped at the MBH. Typical MBHs for 12 in. (- 30 cm) square laminates prepared with 30 mil (0.76 mm) thick interlayer are 10 ft ( -- 3 m) at 0°F (—18 C) and 15 ft ( -- 4.6 m) at 70°F (2I°C). Figure 2 shows a relationship between adhesion and falling ball penetration resistance measured at 2I°C. [Pg.453]

Density and Specific Gravity For binary or pseudobinary mixtures of hquids or gases or a solution of a solid or gas in a solvent, the density is a funcrion of the composition at a given temperature and pressure. Specific gravity is the ratio of the density of a noncompress-ible substance to the density of water at the same physical conditions. For nonideal solutions, empirical calibration will give the relationship between density and composition. Several types of measuring devices are described below. [Pg.764]

FIG. 9-33 Relationship between measured-survival function, number of payback periods, and contribution efBciency. [Pg.835]

Interdiffusion of bilayered thin films also can be measured with XRD. The diffraction pattern initially consists of two peaks from the pure layers and after annealing, the diffracted intensity between these peaks grows because of interdiffusion of the layers. An analysis of this intensity yields the concentration profile, which enables a calculation of diffusion coefficients, and diffusion coefficients cm /s are readily measured. With the use of multilayered specimens, extremely small diffusion coefficients (-10 cm /s) can be measured with XRD. Alternative methods of measuring concentration profiles and diffusion coefficients include depth profiling (which suffers from artifacts), RBS (which can not resolve adjacent elements in the periodic table), and radiotracer methods (which are difficult). For XRD (except for multilayered specimens), there must be a unique relationship between composition and the d-spacings in the initial films and any solid solutions or compounds that form this permits calculation of the compo-... [Pg.209]

The most accurate - and most popular - method of quantifying matrix effects is to analyze the unknown sample with a similar sample of known composition. The relationship between measured intensity and the content of each sample is, usually, defined by the relative sensitivity factor (RSF) ... [Pg.112]

Eor a non-resonant nuclear reaction with emission of an ion, a depth scale can be obtained from the measured energy of the emitted ions. If ions emitted from a depth x are lower in energy by AE than ions emitted from the surface, a relationship between AE and x can be found, similarly to RBS and ERDA analysis ... [Pg.171]

The Yukawa-Tsuno r values have been measured for the solvolysis reactions fonning benzyl cations and several a-substituted derivatives, 6-3IG charges and bond orders have been calculated for the presumed cationic intermediates. Analyze the data for relationships between r and the structural parameters. (Hint. Plot r versus the bond orders and the charges at C-1, C-2, C-3, and C-4.)... [Pg.348]

There have been numerous studies of the rates of deprotonation of carbonyl compounds. These data are of interest not only because they define the relationship between thermodynamic and kinetic acidity for these compounds, but also because they are necessary for understanding mechanisms of reactions in which enolates are involved as intermediates. Rates of enolate formation can be measured conveniently by following isotopic exchange using either deuterium or tritium ... [Pg.419]

The major problem in this procedure is not in obtaining an accurate value for the solute diffusivity from peak width measurements (which is relatively straightforward) but in identifying the best relationship between diffusivity and molecular weight to employ in the subsequent data processing. [Pg.335]


See other pages where Relationship between measured and is mentioned: [Pg.29]    [Pg.64]    [Pg.359]    [Pg.18]    [Pg.1177]    [Pg.289]    [Pg.29]    [Pg.64]    [Pg.359]    [Pg.18]    [Pg.1177]    [Pg.289]    [Pg.206]    [Pg.1894]    [Pg.2651]    [Pg.614]    [Pg.194]    [Pg.300]    [Pg.310]    [Pg.214]    [Pg.378]    [Pg.327]    [Pg.560]    [Pg.709]    [Pg.76]   


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