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Sampling density

Volumen and Hydratationswarme der lonen. Zeitschrift filr Physik 1 45-48. aan C M and K B Wiberg 1990. Determining Atom-Centred Monopoles from Molecular Electro-itic Potentials. The Need for High Sampling Density in Formamide Conformational Analysis. imal of Computational Chemistry 11 361-373. [Pg.266]

Notwithstanding the possibility of such automation, many successful operations depend almost entirely on manual sampling. Density determinations of the pulp on the media-return line and on each of the drainage screens are made at scheduled intervals, and the operator adjusts the media flow as needed. [Pg.1791]

CM Breneman, KB Wiberg. Determining atom-centered monopoles from molecular electrostatic potentials. The need for high sampling density m formamide conformational analysis. J Comput Chem 11 361-373, 1990. [Pg.412]

In lower pressure environments, the wave profiles are dominated by the consequences of deformation of the samples to fill the voids. This irreversible crush-up process strongly controls the wave speeds, which have anomalously low values at low initial sample densities. Modeling of this problem is... [Pg.50]

Fig. 2.22. At very high pressures the observed pressure-volume relations of porous samples show expansions due to the very high temperatures produced in collapsing the voids. The figure shows representative behavior at porous sample densities of 25% to 100% of solid density. Fig. 2.22. At very high pressures the observed pressure-volume relations of porous samples show expansions due to the very high temperatures produced in collapsing the voids. The figure shows representative behavior at porous sample densities of 25% to 100% of solid density.
The detn of APD s between 100 and 500 microns can be made using a permeability app larger than the Fisher Sub-Sieve Sizer. This app, which was developed at PicArsn, uses a sample size of approx TO times the sample density (Ref 7a)... [Pg.528]

Thus, the interaction of the primary beam with the sample provides a wealth of information on morphology, crystallography and chemical composition. Using transmission electron microscopy to make a projection of the sample density is a routine way to study particle sizes in catalysts. [Pg.144]

Both the INTERFEROMETER method (d) and the MIRROR REFLECTION (e) methods use optical means to detect changes in linear expansion of the sample under test. The instrumentation is more complex and will not be described here. The other two methods, X-RAY LATTICE CONSTANTS (f) and SAMPLE DENSITY (g) have not been employed to any great extent for determination of ttL... [Pg.397]

Because the sample density and the values of p/p vary with the composition of the specimen, the complete absorption correction procedure is an iterative process. [Pg.159]

Breneman, C. M. and K. B. Wiberg. 1990. Determining Atom-Centered Monopoles from Molecular Electrostatic Potentials. The Need for High Sampling Density in Formamide Computational Analysis. J. Comp. Chem. 11, 361. [Pg.77]

Physical correction, n - a type of post processing where the correction made to the numerical value produced by the multivariate model is based on a separate physical measurement of, for example, sample density, sample pathlength, or particulate... [Pg.511]

Raman sensors can be used for all three physical states. It possible to measure gases, though at the expense of sensitivity due to the lower sample density, liquids and solids of different forms and shapes. Basically any Raman active substance could be detected, also in aqueous solution, provided substance and the sample matrix permit Raman measurements (fluorescence problem, absorption,. ..) and the analyte concentrations are sufficiently high. [Pg.147]

The Canadian maritime component of the NASGLP consists of 171 sites and the US component is comprised of 180 sites. Nominal sample densities were one site per 1600 km2 in the United States and one site per 800 km2 in Canada. Not all sites provided sufficient material to undertake chemical analyses for all horizons. [Pg.181]

Sampling and analytical methods Locations for the outlet sediment (overbank) samples are shown in Figure 1. In all, 99 catchments were sampled giving an average sample density of 1 site/1540 km2. At most sites three samples were taken (a) a top outlet sediment (TOS) from 0-10 cm depth (b) a bottom outlet sediment (BOS) from 60-90 cm depth and (c) a shallow outlet sediment (SOS) from 10-25 cm depth specifically for MMI determinations. Two size fractions (<180 pm and <75 pm) were prepared from the TOS and BOS samples. The SOS sample for multi-element MMI (MMI-M) analysis by method ME-MS17 was provided to ALS Chemex in its bulk form. [Pg.233]

Collect catchment outlet (overbank) sediment samples from 1400 large catchments covering >90% of Australia using an ultra low sampling density approach to keep costs down ... [Pg.394]


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See also in sourсe #XX -- [ Pg.180 , Pg.276 ]

See also in sourсe #XX -- [ Pg.197 , Pg.209 , Pg.230 , Pg.341 ]




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Candidate density acceptance-rejection-sampling

Data and Sampling Densities

Density of sampling

Kernel sampling density

Packing Density of Sample

Population density measurement sampling

Sample Density Problems

Sample density

Sample packing density

Sampling Low-Density Populations

Software sample density correction

Surface charge density sample problem

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