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Identification of samples

The identification of sampling requirements involves specifying the sampling design, the sampling method, sample numbers, types, and locations, and the level of sampling quality control. Data quality requirements include precision, accuracy, representativeness, completeness, and comparability. [Pg.598]

Table 1 Identification of sampling sites of the RCSP in the Ebro River basin... Table 1 Identification of sampling sites of the RCSP in the Ebro River basin...
Rottlander, R.C.A. and Schlichtherle, H. (1979). Food identification of samples from archaeological sites. In Proceedings of the 22nd Symposium on Archaeometry, ed. Aspinall, A. and Warren, S.E., University of Bradford. Bradford, pp. 218-223. [Pg.405]

On occasion a partial detonation may take place, resulting in large visible quantities of explosive being left at the scene in this event collection and subsequent identification of samples is relatively straightforward. However most explosions only leave invisible residues of unconsumed explosive at the scene. The first problem then is to find the right place from which to take samples. Of course, it wiU be necessary to have a stock of sampling and packaging materials available, which have been quality assured to ensure they are free from any possible traces of explosive so that the validity of any subsequent tests can be established. [Pg.228]

The time required by a given analyte to migrate under the sole influence of the applied electric field across the capillary tube from the injection end of the capillary to the detection windows (migration distance) is defined as the migration time (tj and, similarly as the retention time in HPLC, is used for identification of sample components. It is given by... [Pg.178]

To properly accession and purify nucleic acids for analysis, the receiving laboratory must know the sample type. Both heparin and urine have been reported to inhibit PCR, to the detriment of blood samples containing the former and nearly all samples of the latter. In recent years, extraction technology and amplification chemistry have improved so that each sample type is susceptible to analysis. Proper identification of sample type provides the receiving laboratory with an opportunity to apply appropriate techniques to its extraction and analysis. [Pg.192]

Marker. A reference component which is chromatographed with the sample to aid in the identification of sample components. [Pg.27]

The spectral characteristics of a standard can be monitored during HPLC using a diode-array detector (unitfu). A directory of standard spectra can be stored, enabling additional identification of sample peaks. The actual absorption maxima and fine structure will be dependent on the composition of the mobile phase (see Fig. F2.2.4). Peak I may only occur as a shoulder with civ-carotenoids. while an additional peak is observed at around 340 nm (see Fig. 2.2.1). [Pg.854]

In conclusion, it could be affirmed that the application of an electronic nose can be turned to the identification of samples not conform , or rather samples that have some defects or alterations that differentiate them partly from the standard production recognized by the Disciplinary of Production. [Pg.1091]

Collecting samples - including procedures for taking representative samples, preventing cross contamination among samples, and identification of samples... [Pg.53]

There are a variety of techniques currently in use to aid in the identification of sample components. Most techniques, such as spiking and the enzyme peak shift method, are used to confirm the identities of components thought to be in the sample. If, however, the identity of the sample is truly unknown, a combination of techniques is needed to provide a unique fingerprint. ... [Pg.214]

There are a variety of techniques available to aid in the identification of sample components matching retention times, standard addition, internal standard, isotopic labeling, enzyme peak shift, and UV and mass spectral libraries. [Pg.239]

The validity of any comparative study is dependent on the reliability of the identification of the samples in the study. Not all researchers are experts in the field of identification of samples, nor do all researchers have quick and ready access to expert systemetists who can accomplish the task of identification. The importance of verification of sample identity for comparative studies is vital. We describe several methods by which researchers can obtain and identify samples from the wild, and we suggest methods by which voucher samples can be obtained for future reference to these collected samples. We outline alternatives to collection of samples from the wild, such as purchase from stock centers and biological supply companies. Museum collections can also be extremely helpful in obtaining complete organismal samples for comparative studies. [Pg.65]

Techniques in clinical analysis have undergone many advances in the last few decades. The basic needs in clinical chemistry are unambiguous analyte-specific assays that provide both identification of sample components and their concentration levels. The importance of this is self-evident, since most substances analyzed are part of a multicomponent biological fluid. Advances in enzyme and immunochemical assay techniques provide ideal systems for component... [Pg.35]

Since a spectrum is determined by the structure of the sample, which in turn is a con-.sequence of the forces (and particularly the intermolecular forces in the solid state), this technique is able to provide two-fold information. An introduction to the application of the discussed methods towards the investigation of intermolecular forces is provided in Sec. 5.2, including a short review of the quality which can be obtained. Another obvious application is the identification of samples. Table 4.5-1 demonstrates clearly that, if the formula is known, the spectra provide an indication of the phase of a sample. By using micro-techniques it is possible to identify samples or parts of samples in fields ranging as widely as geology, medicine (kidney stones), pharmacy, electronics, painting (mineral pigments), and materials research. [Pg.322]

The value of N /Nr can be assessed or found by iterative application of eq. (16.4). For constant values of t (the same age of samples), the plot of N2/Nr as a fimction of Ni/Nr gives a straight line with slope (e — 1) intersecting the ordinate at N2/Nr. Such a plot is called an isochrone and is used for evaluation, in particular for identification of samples of the same age. [Pg.329]

Identification of sample components based solely on migration time in capillary electrophoresis (CE) requires reproducibilities not normally obtained. These are caused, mainly, by two effects temperature effects and electro-osmotic affects. Migration times in CE are determined by the electro-osmotic velocity Ueof and effective electrophoretic migration velocity Ueef the net migration velocity Vt is the vector sum of both velocities ... [Pg.999]

The coupled TLC-FAB-MS, without the prior recovery of analyte from the TLC plate, provides a powerful tool for the unambiguous identification of sample components. The use of tandem MS-MS represents a further refinement of this approach, enabling identification to be performed even when the separated components are incompletely resolved from each other or are subject to background interference. [Pg.1624]

The quality control and assurance measures for paternity testing are similar to those for other types of human identity testing. Positive identification of samples, prevention of DNA contamination, the use of control alleles of known size, and the validation of software employed for genetic analysis and calculation are among measures common to identity testing programs. Population distribution data for the systems used must be documented. In addition, mutation frequencies of the systems used must be dociunented and used appropriately. [Pg.1552]

The development of the first HPLC system with MW-triggered fraction collection was described by Zeng et al. [50] at CombiChem. This system was a dual analytical-preparative instrument with parallel-column format, termed parallel Analyl/PrepLCMS." developed by the modification of commercially available instrumentation. This system had software-controlled valves that applied sample to each path from a single autosampler and had the capacity to purify and analyze more than 100 samples per day. Initial analytical LC-MS data acquired by the system allowed the identification of samples that require... [Pg.195]

Rottlander. R.C.A., and Schhchtherle, H. 1979. Food identification of samples from archaeological sites. Archaeo-Physika 10 260-267. [Pg.294]

Identification of sample atmosphere, flow rate, and purity... [Pg.49]

A widely applied discipline of chemometrics is pattern recognition, which involves the classification and identification of samples. Its purpose is to develop a semiquantitative model that can be applied to the identification of unknown sample patterns. To assure the best reliability, pattern recognition requires the applications of a minimum of two analytical methods. The ammonium-azonium tautomerism in /V, /V-d i a I ky I a minoazo dyes used as indicators requires three techniques UV-Vis, IR, and Raman spectroscopy.223 A study of the matrix composition concerning the ratio of the compounds is necessary as well. The application of pattern recognition analysis in geochemical techniques not only assures better reliability but is also quite useful in addressing real-world environmental problems.224... [Pg.61]

The application of KGCM is recommended for accomplishing the following tasks (1) identification of sample compounds (2) quantitative analysis of compounds (usually isomers) differing widely in reactivity (3) enhancing the sensitivity of analytical determinations and (4) extending the area of analysis (analysis of non-volatile compounds that form volatile compounds as a result of a reaction). It should be pointed out that the theory of typical organic reactions is now fairly well developed and a wealth of experimental data have been accumulated, which permits sufficiently reliable determinations of relative rates of chemical reactions, for example, with compounds that differ in the nature and position of the aromatic substituents [8—13]. [Pg.68]

First one component is fed into the reactor column in a pulsed maimer, then a second one after a certain interval. The reaction proceeds during the time interval when the second component overtakes the first one in the column. The use of this method as applied to the qualitative identification of sample components has been described elsewhere [41]. The application of the method for determining the kinetic characteristics was proposed by Berezkin [55]. The method was developed in earlier work [61 ]. [Pg.74]

General problems with the identification of sample compounds by hydrogenation methods were specially considered by Franc and KolouSkova [84], who showed that the vaiu log (where F and F are the retention volumes of the initial and hydro-... [Pg.148]


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See also in sourсe #XX -- [ Pg.322 ]




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