The Application of Atomic Absorption Method as a Flow Detector to Gel Chromatography

1973 ◽  
Vol 6 (7) ◽  
pp. 595-601 ◽  
Author(s):  
Norimasa Yoza ◽  
Shigeru Ohashi
1965 ◽  
Vol 48 (6) ◽  
pp. 1100-1103
Author(s):  
C H Mcbride

Abstract The atomic absorption method studied last year was re-examined and extended to include calcium and sodium. The procedures were submitted to 16 collaborators for determination of Ca, Cu, Fe, Mg, Mn, Na, and Zn. Results for Ca and Na were discouraging; further study is recommended.


1971 ◽  
Vol 14 (4) ◽  
pp. 416-418
Author(s):  
N. K. Rudnevskii ◽  
V. T. Demarin ◽  
T. M. Gruzdeva

1972 ◽  
Vol 55 (5) ◽  
pp. 989-990
Author(s):  
S R Koirtyohann

Abstract An atomic absorption method for the determination of molybdenum in fertilizers was tested collaboratively. The results indicate that additional work is needed to improve precision at low molybdenum levels and to test for a possible positive bias in the method.


1981 ◽  
Vol 64 (2) ◽  
pp. 265-269
Author(s):  
Dennis H Cox ◽  
Ann E Bibb

Abstract A hydrogen selenide (H2Se) evolution-electrothermal atomic absorption method is described for determining nanogram concentrations of total selenium (Se) in biological and environmental materials. A mixed acid digestion procedure is used to decompose organic material. Sodium borohydride, a redesigned hydride generator, and an electric-heated absorption tube are used for H2Se evolution and conversion to atomic Se. The method has a detection limit of 4 ng/mL and a sensitivity of 0.6 ng/mL, and is linear from 0 to 90 ng Se/mL. As determined on urine, water, and bovine liver, total and within-run precision had relative standard deviation values of 5-17.2 and 5.5-12.6%, respectively. Accuracy was established with 2 NBS and 3 EPA reference materials, and mean errors of 0 to +0.8 were obtained. Mean recoveries of 109 and 101% were obtained for 10 and 50 ng Se added to human urine.


1962 ◽  
Vol 59 (3) ◽  
pp. 381-385 ◽  
Author(s):  
C. H. Williams ◽  
D. J. David ◽  
O. Iismaa

A rapid and accurate atomic absorption method for the determination of chromium in faeces samples from pasture experiments using chromic oxide ‘markers’ is described. Of the elements present after ashing and digesting the samples in a phosphoric acid—manganese sulphate—potassium bromate solution silicate, aluminium, calcium and magnesium were found to interfere in the determination. The effects of these interferences were overcome by the addition of calcium to the test solution and by the addition of silicate to the standards, which were prepared in ‘blank’ solutions.The sensitivities of a number of alternate chromium resonance lines relative to that of Cr 3578·7 Å. are given. These lines may be used to increase the concentration range of the analysis.The results of a comparison of the atomic absorption method with a chemical method are given.


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