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Screening qualitative

One procedure makes use of a box on whose silk screen bottom powdered desiccant has been placed, usually lithium chloride. The box is positioned 1-2 mm above the surface, and the rate of gain in weight is measured for the film-free and the film-covered surface. The rate of water uptake is reported as u = m/fA, or in g/sec cm. This is taken to be proportional to - Cd)/R, where Ch, and Cd are the concentrations of water vapor in equilibrium with water and with the desiccant, respectively, and R is the diffusional resistance across the gap between the surface and the screen. Qualitatively, R can be regarded as actually being the sum of a series of resistances corresponding to the various diffusion gradients present ... [Pg.146]

Qualitative Values. The Green Screen qualitative values are derived primarily from the US EPA DfE Program s threshold values. [Pg.21]

FIGURE 18. Pretesting procedures for deciding what chemicals to test qualitatively. Two of these procedures should enrich the chemicals that are to be screened qualitatively and thereby keep down the number of false positives. [Pg.448]

M. Irving, J. Cournoyer, R.S. Li, C. Santos and B. Yan, Qualitative and quantitative analyses of resin-bound organic compounds. Comb Chem High Throughput Screening 4 353-362 2001. [Pg.79]

This section describes how both hypothetical and real accidents are analyzed. These methods varying greatly in complexity and resource requirements, and multiple methods may be used in an analysis. A simple method is used for screening and prioritization followed by a more complex method for significant accident scenarios. Some methods give qualitative results more complex methods give quantitative results in the form of estimated frequencies of accident scenarios. The process systems in Figures 3.3.1-1 and 3.3.1-2 are used in the examples. [Pg.76]

C -CP-MAS NMR provides subtle information about the degree of solvation of the polymer chains of a CFP in a given solvent and consequently it may be qualitatively correlated with the nanometer scale morphology of the polymer matrix. In fact, the prerequisite that enables a polymer framework to develop a nanoporosity is the ability of the polymer chains and its pendants to be suitably solvated by the liquid medium [26-28]. Therefore, C -CP-MAS NMR spectra provide the basis for a first level screening of the possibility of a CFP in a given solvent to be employed as an hexo-template, able to accommodate metal nanoclusters chemically produced in its interior (see below and Ref. [29]). [Pg.202]

From an analysis of the key properties of compounds in the World Dmg Index the now well accepted Rule-of-5 has been derived [25, 26]. It was concluded that compounds are most Hkely to have poor absorption when MW>500, calculated octanol-water partition coefficient Clog P>5, number of H-bond donors >5 and number of H-bond acceptors >10. Computation of these properties is now available as a simple but efficient ADME screen in commercial software. The Rule-of-5 should be seen as a qualitative absorption/permeabiHty predictor [43], rather than a quantitative predictor [140]. The Rule-of-5 is not predictive for bioavail-abihty as sometimes mistakenly is assumed. An important factor for bioavailabihty in addition to absorption is liver first-pass effect (metaboHsm). The property distribution in drug-related chemical databases has been studied as another approach to understand drug-likeness [141, 142]. [Pg.41]

Methods and analytical results are often classified loosely as quantitative, semi-quantitative or qualitative (screening). These categories do not have well-defined or universally accepted boundaries. Since comparison of residue concentrations with legal limits requires exact quantitative results, the validation of quantitative methods is discussed here. [Pg.95]

Assessment and definition of sensitivity are often described for quantitative analysis but are of equal importance for qualitative devices of the dip-stick type that are very popular for farm- or field-based screening assays. Because of the somewhat subjective nature of visually assessed assays, the assay s sensitivity must be validated using a number of observers to determine at what level a test is deemed positive. The number of false positives and false negatives must be carefully determined in order to balance consumer safety and potential economic loss to animal producers. [Pg.691]

It should be emphasized that qualitative consequence screening should only remove from further consideration those buildings where there is significant industry experience to support the assessment. In Example 5 cited above, a long and successful operating history exists to support the... [Pg.22]

Because few generic frequency data were available on VCEs in similar facilities, a risk screening per Chapter 4 of this book was not performed. Instead, as a next step, the decision was made to perform a qualitative risk assessment. [Pg.44]

Site-specific consequence screening for explosion can be performed either qualitatively or quantitatively, depending upon the explosion potential of the materials being handled, as well as processing conditions and other site-specific factors. In performing a consequence screening, it is necessary to select "Evaluation-case" events for consideration. This is defined as follows ... [Pg.96]

Qualitative Consequence Screening Based on Site-Specific Conditions... [Pg.96]

Qualitative frequency evaluation can be used to screen out events that are extremely unlikely to occur (i.e., have such a remote chance of occurring that further evaluation is unnecessary). This method is particularly appropriate for use in conjunction with qualitative consequence evaluation as a means of ranking risks. [Pg.109]


See other pages where Screening qualitative is mentioned: [Pg.368]    [Pg.368]    [Pg.2522]    [Pg.8]    [Pg.1317]    [Pg.9]    [Pg.47]    [Pg.89]    [Pg.235]    [Pg.118]    [Pg.127]    [Pg.597]    [Pg.341]    [Pg.188]    [Pg.248]    [Pg.678]    [Pg.124]    [Pg.103]    [Pg.526]    [Pg.533]    [Pg.534]    [Pg.255]    [Pg.171]    [Pg.651]    [Pg.680]    [Pg.681]    [Pg.15]    [Pg.40]    [Pg.100]    [Pg.104]    [Pg.110]    [Pg.110]   
See also in sourсe #XX -- [ Pg.2453 ]




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