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Flameless atomic absorption spectroscopy

Jeschke, W.D. Stelter, W. (1976). Measurement of longitudinal ion profiles in single roots of Hordeum and Atriplex by use of flameless atomic absorption spectroscopy. Planta, 128,107-12. [Pg.112]

Findlay, W. J., Zdrojewskl, A., and Qulckert, N. "Pre-atomlzatlon Losses In Flameless Atomic Absorption Spectroscopy". Spectrosc. Lett. (1974), 7, 355-364. [Pg.265]

Le Bihan and Courtot-Coupez [202] used the copper complex and flameless atomic absorption spectroscopy to determine anionic detergents. Crisp [200]... [Pg.401]

Trace levels (10 to 10 g/g of sample) of silver can be accurately determined in biological samples by several different analytical techniques, provided that the analyst is well acquainted with the specific problems associated with the chosen method. These methods include high frequency plasma torch-atomic emission spectroscopy (HFP-AES), neutron activation analysis (NAA), graphite furnace (flameless) atomic absorption spectroscopy (GFAAS), flame atomic absorption spectroscopy (FAAS), and micro-cup atomic absorption spectroscopy (MCAAS). [Pg.111]

GFAAS = graphite furnace (flameless) atomic absorption spectroscopy MCAAS = micro-cup atomic spectroscopy DCOP-AES = direct current plasma-atomic emission spectroscopy HFP-AES = high frequency piasma-torch-atomic emission spectroscopy NAA - neutron activation analyst-, atomic absorption spectroscopy AAS - atomic absorption spectrophotometer XES = X-ray energy spectrometry and SEM - scanning electron microscopy. [Pg.117]

GFAAS = graphite furnace (flameless) atomic absorption spectroscopy TLC = thin layer chromatography HFP-AES = high frequency plasma-atomic emission spectroscopy NAA = neutron atomic analysis ICP-AES = inductively coupled plasma-atomic emission spectroscopy AAS = atomic absorption spectrometry GSE = graphite spectroscopic electrode UV = ultraviolet spectrophotometry PD = photodensitometer and (3,5-diBr-PADAP) = 2(-3,-5-dibromo-2-pyridylazo)-5- diethyl-ami nophenol. [Pg.124]

Bouman AA, Platenkamp AJ, Posma FD. 1986. Determination of aluminum in human tissues by flameless atomic absorption spectroscopy and comparison of references values. Ann Clin Biochem 23 91-101. [Pg.296]

C. Flameless Atomic Absorption Spectroscopy. A Jarrell-Ash Model 810 Dual Monochromator Atomic Absorption Spectrophotometer was used for this work. The instrument was equipped with the Bames Instrument s tantalum ribbon flameless atomizer and a two-... [Pg.100]

Table III shows that two quite different analytical techniques, Flameless Atomic Absorption Spectroscopy and Neutron Activation Analysis, yield equivalent frequencies of detection of firearms discharge residue. Table III shows that two quite different analytical techniques, Flameless Atomic Absorption Spectroscopy and Neutron Activation Analysis, yield equivalent frequencies of detection of firearms discharge residue.
Metal Content. Calcium, sodium, and boron contents of paper samples were determined by using a direct solid-sampling technique in conjunction with flameless atomic absorption spectroscopy (20,24). A Varian Techtron AA-6 spectrophotometer was employed with a model 90 carbon rod atomizer. In addition to the direct solid-sampling technique, calcium content was also determined by digesting samples with concentrated hydrochloric acid for 30 min. [Pg.419]

Flameless atomic absorption spectroscopy using the heated graphite furnace is a sensitive method for analyzing environ-mental samples for trace metals. High salt concentrations cause interference problems that are not totally correctable by optimizing furnace conditions and/or using background correctors. We determined that samples with identical ratios of major cations have trace metal absorbances directly related to their Na and trace metal concentrations. Equations and curves based on the Na concentration, similar to standard addition curves, can be calculated to overcome the trace element interference problem. Concentrations of Pb, Cd, Cu, and Fe in sea water can be simply (ind accurately determined from the Na concentration, the sample absorbance vs. a pure standard, and the appropriate curve. [Pg.134]

Jackwerth E.j Willmer P. G., Hohn R. and Berndt H. (1979) A simple accessory for the determination of mercury and the hydride-forming elements (As, Bi, Sb, Se and Te) using flameless atomic absorption spectroscopy, At Absorpt Newsl 18 66-68. [Pg.326]

What is meant by flameless atomic absorption spectroscopy ... [Pg.11]

The determination of mercury in hair by flameless atomic absorption spectroscopy (Association of Official Analytical Chemists, International, Method 971.21, 16th ed., modified for hair)... [Pg.504]

Kacprzak, J.L and Chvojka, R. (1976) Determination of methyl mercury in fish by flameless atomic absorption spectroscopy and comparison with acid digestion method for total mercury. J. Assoc. Off. Anal. Chem., 59,153-157. [Pg.454]

Davis and co-workers (N2, C4) described a new preconcentrating sampling technique for flameless atomic absorption spectroscopy in which a tungsten alloy wire loop is soaked in the sample solution for a specified period of time. Metal ions are concentrated on the surface of the wire loop, apparently by an ion exchange mechanism. The wire... [Pg.311]

Myron, D.R. Givand, S.H. Nielsen, F.H. Vanadium content of selected foods as determined by flameless atomic absorption spectroscopy. J. Agric. Food Chem.. 1977, 25, 297-300. [Pg.42]

Numerous procedures, by a variety of different instruments, are available to quantify the amount of thallium present in hair, blood, tissue, saliva, and urine (for reviews, see [9,81]). Instrumentation used includes emission spectrography, flame and flameless atomic absorption spectroscopy (AAS), voltammetry, neutron activation analysis, and field desorption mass spectroscopy [13,17,82-90]. Field desorption mass spectroscopy when combined with stable isotope dilution can detect fentomole quantities and has value in that no tissue preparation (other than homogenization) is required [65,82,89], The use of these two methods, however, is restricted to specialized laboratories. [Pg.606]

Recommended Air Volume 960 L Recommended Sampling Rate 2.0 L/min Analytical Procedure Air filter samples are digested with nitric acid. After digestion, a small amount of hydrochloric acid is added. The samples are then diluted to volume with deionized water and analyzed by either flame atomic absorption spectroscopy (AAS) or flameless atomic absorption spectroscopy using a heated graphite furnace atomizer (AAS-HGA). [Pg.1007]

The air-dried spiked filters were digested and analyzed for their cadmium content by flameless atomic absorption spectroscopy using a heated graphite furnace atomizer following the procedure described in Section 3. A five-fold dilution of the spiked filter samples at 2 times the Action Level TWA was made prior to their analysis. The 0.05 to 20 ng/mL cadmium standards were used in the analysis of the spiked filters. [Pg.1015]

Roberts C and Clark J. (1986). Improved determination of cadmium in blood and plasma by flameless atomic absorption spectroscopy. Bulletin of Environmental Contamination and Toxicology, 36, 496-499. [Pg.1053]

Hie time-dependent organ distributions of titanium and vanadium were analyzed by flameless atomic absorption spectroscopy in dried organ specimens after single intraperitoneal administrations of therapeutic doses of titanocene dichloride (I, 60 mg/ kg) or vanadocene dichloride (II, 80 mg/kg) / at time 0. [Pg.166]


See other pages where Flameless atomic absorption spectroscopy is mentioned: [Pg.218]    [Pg.204]    [Pg.260]    [Pg.134]    [Pg.430]    [Pg.121]    [Pg.1172]    [Pg.272]    [Pg.170]   
See also in sourсe #XX -- [ Pg.100 ]

See also in sourсe #XX -- [ Pg.659 , Pg.1172 ]




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