Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Sampling parameters

The features of the spectrum are then converted into sample parameters using an appropriate model of the PL process. A sampling of some of the informadon derived from spectral features is given in Table 1. [Pg.376]

Table 1 Examples of sample parameters extracted from PL spectral data. Many rely on... Table 1 Examples of sample parameters extracted from PL spectral data. Many rely on...
Instrumental and sample parameters error in the wavelength, sample transparency, etc. [Pg.136]

Simulation spectra were generated using parameters that describe the ion beam, target and detector geometry, beam and detector resolution, and sample characteristics. The sample parameters, which include the number of layers and the areal density and atomic composition of each layer were then varied until the simulation conformed to the experimental data. The HIBS spectra were analysed using a modified version of the RBS analysis program. [Pg.96]

Subset of a population that is collected Frank and Todeschini [1994] in order to estimate the properties of the underlying population , e.g., the sample parameters mean x and standard deviation s. In the ideal case of representative sampling, the sample parameter fit the parameter of the population ji and a, respectively. [Pg.323]

Unit Cell Average Ce02/Zr02 Sample Parameter Crystallite Size... [Pg.188]

Figure 21.1 Cumulative frequency plot illustration 25th, 75th percentiles, and the interquartile range. estimate of the population variance. Population means and variances are by convention denoted by the Greek letters p and o2, respectively, while the corresponding sample parameters are denoted by X and s2. Figure 21.1 Cumulative frequency plot illustration 25th, 75th percentiles, and the interquartile range. estimate of the population variance. Population means and variances are by convention denoted by the Greek letters p and o2, respectively, while the corresponding sample parameters are denoted by X and s2.
Early studies using resins for isolation and analysis of trace organics, such as pesticides, PCBs, and organic acids, from small volumes of water showed excellent recovery and the potential of easy application to environmental samples. Isotherm studies in distilled water were used to define the sampling parameters for quantitative analysis of these compounds. Later, studies using resin samplers for large-volume environmental samples were extrapolated from the early low-volume resin work of Junk et al. (5,14) and Thurman et al. (27) (see Table I). [Pg.271]

Several examples of near- and far-UV CD spectra are given in the figures included in this unit. With current instruments the final spectra exhibit low noise and—provided that the instrument and sample parameters have been optimized—should be true and reproducible within the limits of protein-in-buffer absorbance of < 1. The most frequent source of nonreproducibility of intensity in spectra is the difficulty of determining the protein concentration, particularly of larger proteins that scatter more and of those with a greater tendency to aggregate. [Pg.241]

Be aware that methods used to increase volatile concentration will affect the volatile ratios however, that may be compromised when simply looking for saturation. These methods do not increase volatility for all compounds, so if no peak-area increase is observed, it could possibly be because the volatile s concentration did not increase in the headspace and not because the fiber is saturated. It is acceptable to use different sampling parameters for testing saturation (e.g., using static sampling for saturation test, while using dynamic sampling for experiment). [Pg.1078]

Second, all possible sources of variation should be included in the calibration set. Sample parameters such as crystal size and shape can influence the position, shape, and intensity of Raman bands. Extensive experimentation was necessary to prove that these parameters did not influence this system. [Pg.153]

Sample Parameter Ciye-talline Amorpho-ui Intsphaie... [Pg.77]

The breakthrough volume is defined as the volume of gaseous sample that can be drawn through a sample tube before an analyte is eluted from the tube. Every sorbent has a limited capacity for a given analyte which depends on the characteristics of the sorbent, on the type of compound to be trapped and on certain sampling parameters, like the temperature and the humidity of the air (Bertoni et al., 1981 Brown and Purnell, 1979). Breakthrough of a substance can occur if ... [Pg.11]

From the earlier data, we take the sample parameters as our estimate of the population parameters... [Pg.43]

Normally the true parameters (so-called parent population parameters) of distributions are not known. For empirical distributions they have to be estimated (symbol A) on the basis of a limited number, n, of observations (so-called sample parameters). Estimates of the most important parameters are ... [Pg.28]

The efficiency of the detection system is based on both detector and sample parameters. Detector parameters include the intrinsic detector efficiency, the geometric relation of detector to sample, scattering by the sample support and nearby material, and attenuation between the sample and the detector. Sample parameters include material stopping power based on composition, mass, diameter and thickness type and amount of sample cover and backing and radiation type, energy, decay fraction, and decay rate. [Pg.35]

Sample size and weight, packing density, heat capacity, and heat conductivity are among the sample parameters that may impact the outcome of a thermal analysis. It is important that a small sample be used and that the sample pan fits the sample shape. [Pg.206]

Figure 11 shows experimental dependencies of [r ]/M12 on M12 for PMCS-5 and PMCS-6 samples, parameters a of which are mostly different. As a consequence, conformation parameters and the va-lue of the Kuhn segment, A, values of which are shown in Table 10, are determined [57],... [Pg.190]

The cone calorimeter was developed in the early 1980s by NIST [11]. This method uses 10 by 10 cm specimens that may be up to 5 cm thick. A cone-shaped heater applies a heat flux of up to 100kW/m2 to the top of the sample. Parameters that can be measured include peak and total heat release rate, mass loss and smoke generation. The data obtained from cone calorimetry can be used for engineering purposes. [Pg.689]


See other pages where Sampling parameters is mentioned: [Pg.377]    [Pg.103]    [Pg.221]    [Pg.353]    [Pg.130]    [Pg.96]    [Pg.97]    [Pg.279]    [Pg.222]    [Pg.293]    [Pg.255]    [Pg.69]    [Pg.211]    [Pg.193]    [Pg.84]    [Pg.489]    [Pg.200]    [Pg.595]    [Pg.303]    [Pg.308]    [Pg.907]    [Pg.538]    [Pg.7]    [Pg.167]    [Pg.286]    [Pg.188]    [Pg.203]    [Pg.206]    [Pg.277]    [Pg.267]    [Pg.118]   
See also in sourсe #XX -- [ Pg.84 ]




SEARCH



Computational methods parameter sampling issues

Estimation of Population Parameters from Small Samples

Instrument parameters affecting solid sampling with electrothermal atomizers and vaporizers

Lattice parameters equilibrium samples

Process analysis sampling parameters

Process parameters sample dimensions

Sample size changing parameters

Sample spectral parameters

Sample statistics and population parameters

Sampling dispersion parameters

Selection of Optimal Sampling Interval and Initial State for Precise Parameter Estimation

Transition path sampling parameters

© 2024 chempedia.info