Big Chemical Encyclopedia

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

Articles Figures Tables About

Ultra-trace

From a toxicological and physiological point of view, the determination of very small amounts of tellurium is becoming increasingly important. Interest is environmental and human health has promoted development in analytical techniques and methods for the trace and ultra trace levels (see Trace AND RESIDUE ANALYSIS). [Pg.388]

Direct multi-element or multi-component simultaneous determination of ultra-trace matter in samples of environmental concern. [Pg.23]

Concentration Minor, trace Major, minor. Ultra-trace Minor, trace... [Pg.606]

Other means are available to study highly reactive intermediates that may be present at trace and ultra-trace levels. One may attempt to divert the intermediate from its normal course. We call this a trapping or scavenging experiment. If T symbolizes a species that rapidly reacts with intermediate I, one possible scheme is then... [Pg.102]

Joarmon S, Pin C (2001) Ultra-trace determination of Ra in thermal waters by high sensitivity quadrapole ICP-mass spectrometry following selective extraction and concentration using radium-specific membrane disks. J Anal At Spectrom 16 32-37... [Pg.57]

ULTRA TRACE ANALYSIS High-purity materials for microelectronics... [Pg.30]

According to the demands of the analysis, analytical chemistry can be classified into analysis of major components (major component analysis, precision analysis, investigation of stoichiometry), minor components, and trace components (trace analysis, ultra trace analysis). On the other hand, analytical problems are differentiated according to the number of analytes involved. Accordingly, single component and multicomponent analysis are distinguished. [Pg.34]

Sometimes it is necessary to apply two (or more) variants of sample preparation to get different measuring samples from only one test sample. This is the case if various problems have to be solved, e.g. determination of major- and ultra trace constituents, comparison of depth- and surface profiles, or analysis of inorganic and organic trace components in the same test sample. An example is shown in Fig. 2.10 where in a test sample of wine both inorganic and organic trace constituents have to be determined and, therefore, different measuring samples must be prepared. [Pg.53]

Of interest for analytical chemistry are at least two further distributions, the logarithmic normal distribution for analytical results at the trace- and ultra-trace level, and the Poisson distribution for discrete results (e.g., counts of impulse summator in XRF). [Pg.99]

Especially in the case of biochemical and environmental systems and generally in ultra trace analysis, SAM is frequently applied. By addition of standard solutions to the sample a similar behaviour of the calibration set and the sample is created provided that the analyte is added in form of... [Pg.172]

Although standard addition calibration is an unreliable method if linearity in the range x < x0 is not experimentally verified but only supposed, there is scarcely an alternative in trace and ultra trace analysis when matrix effects are seriously suspected. [Pg.173]

Results of ultra trace analyses are sometimes characterized by relatively high uncertainties up to more than 100%. In such cases it is not allowed that the lower uncertainty limit falls below zero. Results like, e.g., (0.07 0.10) must be replaced by such as (0.07 + 0.10/ — 0.07) or (0.07/q o°), respectively. That means, the total uncertainty interval (confidence interval, prediction interval is 0...0.17). In general, when the confidence interval includes a negative content (concentration), the result has to be given in the form... [Pg.243]

Ma Y, Zhou M, Jin X et al (2004) Flow-injection chemiluminescence assay for ultra-trace determination of DNA using rhodamine B-Ce(IV)-DNA ternary system in sulfuric acid media. Anal Chim Acta 501 25-30... [Pg.64]

W. Kutschera, Progress in isotope analysis at ultra trace level by AMS, Ini. J. Mass Spectrom., 242, 145 160 (2005). [Pg.481]

It was generally agreed that any determinations of trace metals carried out on seawater prior to about 1975 are questionable, principally due to the adverse effects of contamination during sampling, which were then little understood and lead to artificially high results. It is only in the past few years that methods of adequate sensitivity have become available for true ultra-trace metal determinations in water. [Pg.4]

Increasingly used for sample clean-up prior to chromatographic analysis and pre-concentration of trace and ultra-trace levels of analytes. Largely replacing solvent extraction. [Pg.70]

A multidisciplinary effort is required to design and build instruments with previously unavailable capabilities for demanding new applications. Instruments with more sensitivity are required today to analyze ultra-trace levels of environ-... [Pg.545]

Oehme, M., et al. (1993). The ultra trace analysis of polychlorinated dibenzop-dioxins and diben-zofurans in sediments from the Arctic (Barents Sea) and Northern North Sea. Methodology and quality assurance. Analytical methods and instrumentation, 1, 153-163. [Pg.432]

A great deal of discussion about elemental determination methods focuses on minor, trace, ultra-trace levels of analyte presence in relatively large volume samples. There is another area equally challenging and that involves elemental determination at major and minor concentration in very small volume/low mass samples. Lochmuller and Galbraith used PIXE to study the metal content of carbonic anhydrase... [Pg.258]

Laser ablation ICP-MS (LA-ICP-MS) was established in the early 1990s as a potential routine tool for the measurement of trace and ultra-trace elements in silicate systems for geology. Early studies (Perkins et al. 1993) used sample preparation techniques identical to that used to prepare rock samples for WDXRF, i.e., either a pressed powder disk or a glass bead fusion method (see Appendix VIII). Such studies concluded that LA-ICP-MS had the potential to surpass XRF in terms of the limits of detection achieved and INAA in terms of the speed of analysis (Perkins et al. 1993 481). It has long been recognized that the main limit on the quantitative performance of LA-ICP-MS is the homogeneity at the trace and ultra-trace level of the solid calibration standards available. Subsequent work (e.g., Hollecher and Ruiz 1995, Norman et al. 1996) has demonstrated that some of the international... [Pg.135]

Jarvis, K. E. (1988). Inductively coupled plasma mass spectrometry a new technique for the rapid or ultra-trace level determination of the rare-earth elements in geological materials. Chemical Geology 68 31-39. [Pg.370]

Perkins, W. T., Pearce, N. J. G., and Jeffries, T. E. (1993). Laser ablation inductively coupled plasma mass-spectrometry - a new technique for the determination of trace and ultra-trace elements in silicates. Geochimica et Cosmochimica Acta 57 475—482. [Pg.378]


See other pages where Ultra-trace is mentioned: [Pg.467]    [Pg.178]    [Pg.67]    [Pg.287]    [Pg.416]    [Pg.588]    [Pg.648]    [Pg.661]    [Pg.667]    [Pg.95]    [Pg.927]    [Pg.441]    [Pg.78]    [Pg.512]    [Pg.605]    [Pg.425]    [Pg.435]    [Pg.101]    [Pg.82]    [Pg.5]    [Pg.5]    [Pg.5]    [Pg.5]    [Pg.6]    [Pg.8]    [Pg.9]    [Pg.16]   
See also in sourсe #XX -- [ Pg.37 , Pg.40 ]




SEARCH



Elements, essential ultra trace

Ultra-trace TNT Detection with Operable Devices

Ultra-trace element

© 2024 chempedia.info