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Minimal detection limit

In the presented work an algorithm for the primary radiation filter optimization has been developed and realized in the Mathcad envelope which provides a minimal detection limit of a critical element both at the given X-ray tube power and at the given maximal acceptable count rate. [Pg.134]

Third, assays need to describe methods used for obtaining minimal detection limits (e.g., mean plus 3 SD of 20 replicates of a zero calibrator) and total imprecision, describing at what concentration a 10% CV is attained. Preanalytical factors that should be described include the effects of storage time and temperature, glass versus plastic tubes and gel separator tubes, and the influence of anticoagulants and whole blood measurements. As more assay systems are devised for POCT, the same rigors applied to the central laboratory methodologies need to be adhered to by the POCT systems. [Pg.1637]

An alternative expression for the detection limit, which minimizes both type 1 and type 2 errors, is the limit of identification, (Sa)loi> which is defined as... [Pg.95]

Highly sensitive iastmmental techniques, such as x-ray fluorescence, atomic absorption spectrometry, and iaductively coupled plasma optical emission spectrometry, have wide appHcation for the analysis of silver ia a multitude of materials. In order to minimize the effects of various matrices ia which silver may exist, samples are treated with perchloric or nitric acid. Direct-aspiration atomic absorption (25) and iaductively coupled plasma (26) have silver detection limits of 10 and 7 l-lg/L, respectively. The use of a graphic furnace ia an atomic absorption spectrograph lowers the silver detection limit to 0.2 l-ig/L. [Pg.91]

Relative width of region of unreliable reaction (5) was estimated as the ratio of difference between maximum and minimal concentrations to minimal concentration in this region. The test-system containing Co [Fe(CN)g] is the most resistant to uncontrolled factors, the lowest detection limit characterizes a film with Ni,[Fe(CN)J. The possibility of test-films application for quantitative determination of nitroxoline is testified. [Pg.325]

Most of the transition elements that are of primary interest in the semiconductor industry such as Fe, Cr, Mn, Co, and Ni, can be analyzed with very low detection limits. Second to its sensitivity, the most important advantage of NAA is the minimal sample preparation that is required, eliminating the likelihood of contamination due to handling. Quantitative values can be obtained and a precision of 1-5% relative is regularly achieved. Since the technique measures many elements simultaneously, NAA is used to scan for impurities conveniently. [Pg.672]

A staggering number of papers are published each year in the literature on various candidate chemical/biological detection systems. Researchers and manufacturers make diverse claims of detection limits, sensitivity, false-alarm rates, and robustness for these systems. The committee believes that in many cases, researchers emphasize the strengths of their particular detection systems while minimizing or ignoring their flaws. This practice makes it virtually impossible to evaluate the likely performance of a detection system in real-world air transportation environments. [Pg.16]

CE has been used for the analysis of anionic surfactants [946,947] and can be considered as complementary to HPLC for the analysis of cationic surfactants with advantages of minimal solvent consumption, higher efficiency, easy cleaning and inexpensive replacement of columns and the ability of fast method development by changing the electrolyte composition. Also the separation of polystyrene sulfonates with polymeric additives by CE has been reported [948]. Moreover, CE has also been used for the analysis of polymeric water treatment additives, such as acrylic acid copolymer flocculants, phosphonates, low-MW acids and inorganic anions. The technique provides for analyst time-savings and has lower detection limits and improved quantification for determination of anionic polymers, compared to HPLC. [Pg.278]

Principles and Characteristics The prospects of Raman analysis for structural information depend upon many factors, including sample scattering strength, concentration, stability, fluorescence and background scattering/fluorescence from the TLC substrate. Conventional dispersive Raman spectroscopy has been considered as a tool for in situ analysis of TLC spots, since most adsorbents give weak Raman spectra and minimal interference with the spectra of the adsorbed species. Usually both silica and cellulose plates yield good-quality conventional Raman spectra, as opposed to polyamide plates. Detection limits for TLC fractions... [Pg.535]

The limit of detection is that analytical value that always will be found, apart from the small risk of error a = fi. The detection limit characterizes analytical procedures with regard to minimal value which can be detected with high significance. The limit of detection can, therefore, be reported as limit content when no signal is found. [Pg.230]

O ring. At 20 min inhibition time the detection limits for malathion, parathion methyl and paraoxon were 3, 0.5 and 5pg I respectively. Although these bienzymatic systems look simple, it is difficult to provide optimal conditions for both enzymes. In general the optimum pH, temperature and buffer molarity for different enzymes are different. The experimental conditions are at the levels below the optimum capacity of both enzymes [14], This disadvantage can be minimized by use of a single enzyme system, which is readily inhibited by the pesticide. [Pg.60]

With the newly proposed detector, Dadoo et al. [84] adapted this bioluminescence reaction to determine ATP. A selective and sensitive determination is achieved because the use of CE as a separation technique minimizes the effect of several interfering substances such as some anions (e.g., SCN, I ) that inhibit the reaction decreasing the luminescence emission, and even some nucleotides that generate light in this reaction but with lower intensity. A detection limit of 5 nM, approximately 3 orders of magnitude lower than using UV detection, was obtained. [Pg.464]


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