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Trace concentration

The foregoing equation reveals that essentially the concentration distribution ratio for trace concentrations of an exchanging ion is independent of the respective solution of that ion and that the uptake of each trace ion by the resin is directly proportional to its solution concentration. However, the... [Pg.1115]

Bromide ndIodide. The spectrophotometric determination of trace bromide concentration is based on the bromide catalysis of iodine oxidation to iodate by permanganate in acidic solution. Iodide can also be measured spectrophotometricaHy by selective oxidation to iodine by potassium peroxymonosulfate (KHSO ). The iodine reacts with colorless leucocrystal violet to produce the highly colored leucocrystal violet dye. Greater than 200 mg/L of chloride interferes with the color development. Trace concentrations of iodide are determined by its abiUty to cataly2e ceric ion reduction by arsenous acid. The reduction reaction is stopped at a specific time by the addition of ferrous ammonium sulfate. The ferrous ion is oxidi2ed to ferric ion, which then reacts with thiocyanate to produce a deep red complex. [Pg.232]

Mechanistic Models. A general theory of the mechanism for the complete heterogeneous catalytic oxidation of low molecular weight vapors at trace concentrations in air does not exist. As with many catalytic reactions, however, certain observations have led to a general hypothesis (17). [Pg.504]

Y. Wang, H. Shaw, and R. J. Farrauto, "Catalytic Oxidation of Trace Concentrations of Trichloroethylene over 1.5% Platinum on alpha-Alurnina," in Ref. 3. [Pg.516]

Mercury generally is found in low and trace concentrations. So there is need to determine Hg in ranges corresponding to various types of water samples. Detection levels of Hg can be improved by the use of vapour generation technique. This technique allows to sepai ate the analyte from the sample matrix and so to overcome the matrix interference. The fluorescence technique, with its high sensitivity and linearity, in combination with vapour generation, provides for a possibility to detect Hg in parts per trillion per liter regions. [Pg.211]

Sputtered Neutral Mass Spectrometry (SNMS) is the mass spectrometric analysis of sputtered atoms ejected from a solid surface by energetic ion bombardment. The sputtered atoms are ionized for mass spectrometric analysis by a mechanism separate from the sputtering atomization. As such, SNMS is complementary to Secondary Ion Mass Spectrometry (SIMS), which is the mass spectrometric analysis of sputtered ions, as distinct from sputtered atoms. The forte of SNMS analysis, compared to SIMS, is the accurate measurement of concentration depth profiles through chemically complex thin-film structures, including interfaces, with excellent depth resolution and to trace concentration levels. Genetically both SALI and GDMS are specific examples of SNMS. In this article we concentrate on post ionization only by electron impact. [Pg.43]

Hydrofluoric acid is highly corrosive to skin and mucous membranes. Even in fairly low concentrations, it causes painful skin burns and severe damage to eyes and the respiratory system. Exposure at higher levels results in destruction of tissues and death. No one in l e.xas City was exposed to more than trace concentrations of hydrofluoric acid. The acid vessel had a capacity of about 850 barrels of which a small fraction was released. [Pg.256]

Small additions of Ce have been shown to have a favourable influence on oxide growth of several Fe-Cr alloys by improving scale adherence and acting as nucleation sites for CrjO, . Levels of Ce as low as 0.024% reduce the carbon uptake of steels in carbonaceous atmospheres by several orders of magnitude. Trace concentrations of As and Sn have been found to improve the breakaway properties of mild and low alloy steels in CO/COj, whereas Cu has been found to be detrimental. ... [Pg.980]

TOF-SIMS can be applied to identify a variety of molecular fragments, originating from various molecular surface contaminations. It also can be used to determine metal trace concentrations at the surface. The use of an additional high current sputter ion source allows the fast erosion of the sample. By continuously probing the surface composition at the actual crater bottom by the analytical primary ion beam, multi element depth profiles in well defined surface areas can be determined. TOF-SIMS has become an indispensable analytical technique in modem microelectronics, in particular for elemental and molecular surface mapping and for multielement shallow depth profiling. [Pg.33]

Rubin HE, M Alexander (1983) Effect of nutrients on the rates of mineralization of trace concentrations of phenol and p-nitrophenol. Environ Sci Technol 17 104-107. [Pg.237]

Rubin HE, RV Subba-Rao, M Alexander (1982) Rates of mineralization of trace concentrations of aromatic compounds in lake water and sewage samples. Appl Environ Microbiol 43 1133-1138. [Pg.237]

Each sample was fortified with chlorpyrifos, as a reference standard, to determine the recovery during each extraction. Three portions of solvent were used, and the combined extract for each sample was dried with sodium sulfate. Analyses employed gas chromatography/flame photometric detection. Limits of detection for vegetation and animal tissues were 0.2 and 0.007 pg respectively. Recoveries from fortified samples were 82%. Diazoxon occurrence was infrequenf and at trace concentrations. [Pg.949]

Numerous studies of broadband oxide semiconductors made in tiie form of a relatively thin monocrystal or a thin film sintered on a dielectric substrate revealed that if oxides ZnO, Ti02, SnC>2, CdO, or similar ones are used, it is possible to determine with sufficient accuracy trace concentrations of such active molecules, atoms and radicals as O2, CI2, Br2, J2, H2, H, N, O, OH, Cl, OH, Cl, CH3, CjHj, C3H7, NHj, NH as well as atoms of many metals (Na, Ag, Zn, Cd, Pb, Fe, Pd, Pt, etc.) without the need of prior activating adsorbates. [Pg.171]

The above results on detection of trace concentrations of oxygen by sine oxide films (and titanium oxide films, to a lesser degree), as well as the results on detection of alkyl radicals, which are acceptors of semiconductor electrons, show that the behaviour and electric properties of... [Pg.266]

Marvin, C. H., Brindle, I. D., Singh, R. P., Hall, C. D., and Chiba, M., Simultaneous determination of trace concentrations of benomyl, carbendazim (MBC) and nine other pesticides in water using an automated on-line pre-concentration high-performance liquid chromatographic method, /. Chromatogr., 518, 242, 1990. [Pg.199]

Over 98% of the soil is made up of only eight major chemical elements, listed in Table 51, in order of decreasing abundance. The 90-odd others make up the remaining 2% many occur in the soil as secondary or minor elements, while a large number of still others are present in only very low, often trace, concentrations. Thus all soils contain main, minor, and trace elements combined into chemical compounds and aggregated into complex particles of varying shape, size, and chemical composition (see Textbox 8). [Pg.246]

L-PGDS is the same protein as (3-trace (Hoffmann et al., 1993 Watanabe et al., 1994), which was originally discovered in 1961 as a major protein of human CSF (Clausen, 1961) and later identified in the seminal plasma, serum, and urine. Therefore, the L-PGDS/(3-trace concentration in body fluids may be a useful clinical marker for various diseases (Urade Hayaishi, 2000a Urade et al., 2002, 2006). The L-PGDS/(3-trace concentrations in seminal plasma, serum, and urine... [Pg.368]

The serum L-PGDS/p-trace concentration shows a circadian variation with a nocturnal increase, which is suppressed during total sleep deprivation but not affected by deprivation of REM sleep (Jordan et ah, 2004). Whether or not L-PGDS is a dual-function protein in vivo and is involved in the production of PGD2 as well as in the transport of PGD2 or some other compound(s) remains to be elucidated. [Pg.369]

As shown schematically in Figure 1, a gas-phase chemiluminescence detector consists of a reaction chamber, inlets for the analyte and reagent gas streams, a vacuum pump to lower the pressure in the reaction chamber (typically to a few torr), and a transducer such as a photomultiplier tube (PMT) to monitor the light produced in the reaction. The reagent gas, usually present in large excess, reacts with a trace concentration of analyte to produce an excited product that subse-... [Pg.351]


See other pages where Trace concentration is mentioned: [Pg.308]    [Pg.433]    [Pg.64]    [Pg.58]    [Pg.170]    [Pg.502]    [Pg.42]    [Pg.319]    [Pg.36]    [Pg.31]    [Pg.825]    [Pg.260]    [Pg.384]    [Pg.415]    [Pg.906]    [Pg.907]    [Pg.612]    [Pg.51]    [Pg.69]    [Pg.39]    [Pg.112]    [Pg.334]    [Pg.27]    [Pg.15]    [Pg.128]    [Pg.927]    [Pg.423]    [Pg.42]    [Pg.43]    [Pg.341]    [Pg.374]   
See also in sourсe #XX -- [ Pg.21 ]




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