Big Chemical Encyclopedia

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

Articles Figures Tables About

Initial screening procedure

If the comparison shows that the measurement is inconsistent with the comparison information, the measurement is considered suspecl. If a measurement can be compared to more than one set of information and found to be inconsistent with all, it is likely that the measurement is in error. The measurement should then be excluded from the measurement set. In this section, validation is extended to include comparison of the measurements to the constraints and initial adjustment in the measurements. Validation functions as an initial screening procedure before the more comphcated procedures begin. Oftentimes, vahdation is the only measurement treatment required prior to interpretation. [Pg.2566]

In the authors and several other OPCW-designa-ted laboratories, LC/MS is used as the initial screening procedure for water samples and aqueous extracts of matrices such as soil. This usually provides a tentative identihcation of polar analytes within half a day, on the basis of molecular mass, any fragment ions present, and retention time. A second analysis, under LC/MS/MS conditions, usually provides a firmer identihcation on the basis of a limited number of product ions, most of which result from simple neutral losses. With clean matrices, the initial screening may be performed even faster using how injection or infusion rather than LC (14). An example of the application of how injection with electrospray ionization/mass spectrometry (ESI/MS) in an OPCW prohciency test is provided by Hooijschuur et al. (21) The identihcation of the analytes is usually conhrmed by GC/MS (in most cases after derivatization) as the second technique. [Pg.291]

There is an obvious order to these four facets of analytical methodology. Ideally, a protocol uses a previously validated procedure. Before developing and validating a procedure, a method of analysis must be selected. This requires, in turn, an initial screening of available techniques to determine those that have the potential for monitoring the analyte. We begin by considering a useful way to classify analytical techniques. [Pg.37]

The evaluation of hazards in a process starts at the initial screening of the process parameters. Several technical issues that will need more attention will arise from this screening procedure. Hazard evaluation procedures, however, are no substitutes for engineering codes of practice and for design standards, but are used as supplementary ideas and concepts. A prerequisite for any process hazard evaluation is a full knowledge of the chemistry of the process (including potential unwanted side reactions) with supporting data. [Pg.176]

Flows within the wake region of buildings are extremely complex and generally applicable equations are difficult to derive. In practice, the estimation of near-field concentrations in complex flows around buildings is best undertaken in a wind tunnel. However this may not be possible in many situations and relatively simple numerical estimates may be required. The following discussion outlines a procedure which is necessarily very approximate but which could be used as an initial screening estimate for concentrations which should be accurate to about a factor of 3. [Pg.251]

With an available diesel emergency generator supplying power to critical pumps, the control room operators initiated shutdown procedures for the two reactor areas. An uninterruptible power supply (UPS) kept power to the DCS screens and instruments however, the DCS system was designed close all catalyst preparation and reactor feed valves on loss of power. Outside operators were sent to manually block in reactor feeds. [Pg.370]

Mouse Bioassay Procedures. For initial screening and LD50 determinations outbred female swiss mice (Harlan Sprague Dawley ICR BR ) weighing between 19 to 21 g were used. Doses of toxic extract were suspended in 0.5 ml of 0.1% Tween 60 in 0.15 M NaCl and administered by i. p. injection. Mice were observed for a period of 48 hours. [Pg.260]

Walter, T. S., et al. (2005). A procedure for setting up high throughput nanolitre crystallization experiments. III. Crystalhzation workflow for initial screening. [Pg.262]

In monitoring food supply for drug residues, any efficient microbiological procedure can be used as an initial screen to detect the presence of a wide range of substances that are inhibitory to the growth of microorganisms. Some informa-... [Pg.782]

Rejection of potentially good candidates can also be avoided if there is a sound procedure in place, preferably one that has stood up well on previous occasions. The work that has already been done at the Job Definition stage, where the critical or key criteria were identified, will be of great help in the initial screening of the applicants. [Pg.30]

On the other hand, the Rotarod Test can be considered only as an initial screen for neuromuscular impairment. More complex tests, for example analyses of gait, are required to further understand the motor aspects, whereas electrophysiological procedures, for example the electromyogram (EMG), are required for better understanding the neuromuscular aspects. [Pg.24]

More elaborate procedures can be employed to assess whether drug withdrawal induces changes in fearfulness, pain sensitivity, convulsive threshold or even memory. On the other hand, it is frequently difficult to demonstrate effects on these parameters and the tests involved are particularly time-consuming. The procedure described below represents an initial screen which has been shown to be sensitive to several dependence-inducing drugs such as opioids and benzodiazepines (Goudie et al. 1993). [Pg.49]

It is in the realm of very large combinatorial libraries that selection rather than screening gains crucial importance. As the focus shifts from randomizing an eight-residue peptide to a 100 amino acid protein (the typical size of a small functional domain, for example a chorismate mutase domain), the number of sequence permutations rises to an astronomical 20100. The ability to assay even a tiny fraction of this sequence space in directed molecular evolution experiments demands selection, even though initial development of an appropriate system may be considerably more involved than the setup of a screening procedure. [Pg.33]


See other pages where Initial screening procedure is mentioned: [Pg.99]    [Pg.300]    [Pg.488]    [Pg.103]    [Pg.478]    [Pg.69]    [Pg.55]    [Pg.619]    [Pg.99]    [Pg.300]    [Pg.488]    [Pg.103]    [Pg.478]    [Pg.69]    [Pg.55]    [Pg.619]    [Pg.465]    [Pg.362]    [Pg.46]    [Pg.1417]    [Pg.216]    [Pg.262]    [Pg.200]    [Pg.98]    [Pg.298]    [Pg.44]    [Pg.51]    [Pg.234]    [Pg.83]    [Pg.1417]    [Pg.331]    [Pg.497]    [Pg.239]    [Pg.93]    [Pg.58]    [Pg.102]    [Pg.61]    [Pg.295]    [Pg.317]    [Pg.2]    [Pg.319]    [Pg.42]    [Pg.191]   
See also in sourсe #XX -- [ Pg.488 ]




SEARCH



Initiation procedure

© 2024 chempedia.info