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Data ranges

To efficiently construct a histogram for grouped data firstly requires the determination of the optimum number of classes the data range is separated into. A suitable... [Pg.278]

From the data range (maximum minus minimum value) the optimum elass width, w, ean then be determined from ... [Pg.280]

Spectroscopic ellipsometers that measure A in the whole data range require an achromatic compensator with a phase shift close to 90° over a large spectral range. The compensator can be located between polarizer and sample or between sample and analyzer. [Pg.268]

Figure 9-55. Capacity correlation for two types of Intalox structured packing. Data range 5 s a s 73 and 0.07 s )i s 1.1. Used by permission of Norton Chemical Process Products Corp., Bull. ISP-2 (1994). Figure 9-55. Capacity correlation for two types of Intalox structured packing. Data range 5 s a s 73 and 0.07 s )i s 1.1. Used by permission of Norton Chemical Process Products Corp., Bull. ISP-2 (1994).
Data range for regular-high tenacity yarns, ref. 124. Ref. 260. [Pg.46]

K(,(., calculated from the octanol-water coefficient (K w) solubility, and melting point data ranged from 2.93 to 3.47, and compared favorably with literature values (Karickhoff 1981). McLean et al. (1988) estimated a lower Kq . of 39, equal to a log of 1.59. More recently, a of 5,100, equal to log 3.7, has been reported (HSDB 1999). These values indicate that methyl parathion is moderately mobile to immobile in soil (Swann et al. 1983). [Pg.152]

If several candidate models are tested for fit to a given data set, it need not necessarily be that all weighting models w(x) g(r,) listed as examples above would indicate the same model as being the best (in the statistical sense), nor that any given model is the best over the whole data range. [Pg.160]

The Fourier transforms for both films are again quite similar, but as for the ex situ measurements, the chromate-passivated films appear to have a more glassy structure. It should be mentioned that these studies employed a rather limited data range which makes spectral differentiation difficult. [Pg.294]

Standard deviation of range Graphic 59-2 R2 versus Sr of data range. [Pg.389]

Figure 4. Accumulation of naphthalene and metabolic products (expressed as naphthol) after exposure of stage V spot shrimp to 8-12 ppb of waterborne [1-14C] naphthalene and [1- 4C]naphthalene complexed with BSA (A), regression lines of concentrations of [l-,4C]naphthalene with sampling points indicated (B), median values of metabolic products with data ranges (47). Figure 4. Accumulation of naphthalene and metabolic products (expressed as naphthol) after exposure of stage V spot shrimp to 8-12 ppb of waterborne [1-14C] naphthalene and [1- 4C]naphthalene complexed with BSA (A), regression lines of concentrations of [l-,4C]naphthalene with sampling points indicated (B), median values of metabolic products with data ranges (47).
Table 2.3 shows the calculated ion concentrations with a concentration factor of 3.33, and compares them with actual plant values. Note that there are significant differences between the calculated and actual ion concentrations for most species, however this is likely to be a result of the plant operating below the stated recovery rate of 70%. The differences in the concentration factors from the actual plant data (ranging from 0.79 for nitrate to 3.03 for sodium) are largely a result of the different precipitation points for each of the species in the water. [Pg.18]

Mg/m (0.03 ppm). The percentage of valid data recovered is also indicated. The absence of some data—ranging up to 17.8% in 1970, but averaging 8.3% during the 7 yr—represents an underestimate that cannot be adjusted with any certainty. The total number of hours with concentrations of 157 (0.08 ppm) or more during June through Sep-... [Pg.601]

Figure 15.3. Once a solution has been obtained, the choice of postprocessing options may be quite varied, with each option requiring different means of accessing the solution data, ranging from one-time access through interactive manipulation of the solution to real-time critical applications, in latter cases requiring recomputation or updating of the solution data. Figure 15.3. Once a solution has been obtained, the choice of postprocessing options may be quite varied, with each option requiring different means of accessing the solution data, ranging from one-time access through interactive manipulation of the solution to real-time critical applications, in latter cases requiring recomputation or updating of the solution data.
Gong and Cao described A. annua SEE of artemisinin (1) in SCCO2 determined by static method at three temperatures (313, 323 and 333 K) and pressures varying between 11 and 31 MPa. The solubility data ranged from 0.498 x 10 to 2.915 x 10 mol/mol under these conditions. Two density-based models (Chrastil s and Mendez-Sanfiago-Teja s) were selected to correlate the experimental data and the average absolute relative deviation was 8.32% and 8.33%, respectively. The correlation results were in agreement with experimental data. [Pg.317]

In addition to the wide range of effects which artificial snow has on the enviromnent (e.g. [46 9]), the loss of evaporation and sublimation resulting from snow cover or snowmaking is of particular relevance for the water balance of alpine catchment areas. The extent of this loss is still unclear. The data range from 10% to 30% of the volume of water used for snowmaking [7, 8]. [Pg.84]

The second step of the dose-response assessment is an extrapolation to lower dose levels, i.e., below the observable range. The purpose of low-dose extrapolation is to provide as much information as possible about risk in the range of doses below the observed data. The most versatile forms of low-dose extrapolation are dose-response models that characterize risk as a probability over a range of environmental exposure levels. Otherwise, default approaches for extrapolation below the observed data range should take into account considerations about the agent s mode of action at each tumor site. Mode-of-action information can suggest the likely shape of the dose-response curve at these lower doses. Both linear and nonlinear approaches are available. [Pg.309]

Figure 8. Heat map of a cluster of BioPrint compounds with similar in vitro ADME profiles. Eight ADME assays are clustered on the X-axis and 8 compounds are clustered on the Y-axis. Normalized data range from 0 (blue-green) to 2 (red). Clustering is performed using Pearson correlation and complete linkage using normalized dataset. Where available in literature, human in vivo oral absorption (oa) and oral bioavailability (ba) values (%) are presented after the compound name. Figure 8. Heat map of a cluster of BioPrint compounds with similar in vitro ADME profiles. Eight ADME assays are clustered on the X-axis and 8 compounds are clustered on the Y-axis. Normalized data range from 0 (blue-green) to 2 (red). Clustering is performed using Pearson correlation and complete linkage using normalized dataset. Where available in literature, human in vivo oral absorption (oa) and oral bioavailability (ba) values (%) are presented after the compound name.

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See also in sourсe #XX -- [ Pg.130 ]




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Coal range, analytical data

Composite data type range

Data type range

Data, temperature range

Experimental Data to Provide Information over Wide Ranges of Time Scale

Interquartile range normalization, data

Laboratory data normal ranges

Liquid data, temperature range

Range of data

Vapor data, temperature range

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