X-Ray Fluorescence Analysis of Tungsten-Molybdenum Metals and Electrolytes

1960 ◽  
Vol 4 ◽  
pp. 474-487
Author(s):  
K. R. Stever ◽  
J. L. Johnson ◽  
H. H. Heady
Keyword(s):  
Internal Standard ◽  
Fluorescence Analysis ◽  
Metal Powders ◽  
Soft Or ◽  
X Ray ◽  
Molybdenum Metal ◽  
Fused Salts ◽  
Hard Radiation ◽  
Impurity Elements

AbstractAn X-ray fluorescence method is presented for the analysis of tungsten-molybdenum solutions. Tungsten and molybdenum metal powders, produced by a fused-salt electrolysis procedure, are dissolved and analyzed for tungsten and molybdenum by using the W La1, Pt La1 intensity ratios. The platinum spectral line from the X-ray tube target serves as a self-internal standard. The sensitivity limit is about 0,05% and in the concentration range of 0.5 to 100%, the accuracy of analysis is within about 2% standard deviation. The technique is also applied to the analysis of tungsten and molybdenum in fused salts and to the determination of several other Impurity elements in these metals.A double detector modification for the General Electric X-ray unit is described. The detector consists of a double-window flow proportional counter tube backed up by a sealed krypton-filled counter tube. This allows counting of either soft or hard radiation at maximum efficiencies without the necessity of changing counter tubes. Advantages in specific applications are discussed.

Sorption of Se (IV) from aqueous solutions with subsequent determination by X-ray fluorescence analysis

2020 ◽  
Vol 86 (10) ◽  
pp. 5-9
Author(s):  
D. G. Filatova ◽  
A. A. Arkhipenko ◽  
M. A. Statkus ◽  
V. V. Es’kina ◽  
V. B. Baranovskaya ◽  
...  
Keyword(s):  
Inductively Coupled Plasma ◽  
Fluorescence Analysis ◽  
Standard Samples ◽  
Phase Contact Time ◽  
Sorbent Phase ◽  
X Ray ◽  
Fundamental Parameters ◽  
Inductively Coupled ◽  
Subsequent Determination

An approach to sorptive separation of Se (IV) from solutions on a novel S,N-containing sorbent with subsequent determination of the analyte in the sorbent phase by micro-x-ray fluorescence method is presented. The sorbent copolymethylenesulfide-N-alkyl-methylenamine (CMA) was synthesized using «snake in the cage» procedure and proven to be stable in acid solutions. Conditions for quantitative extraction of Se (IV) were determined: sorption in 5 M HCl or 0.05 M HNO3 solutions when heated to 60°C, phase contact time being 1 h. The residual selenium content in the solution was determined by inductively coupled plasma mass spectrometry (ICP-MS) using 82Se isotope. The absence of selenium losses is proved and the mechanism of sorption interaction under specified conditions is proposed. The method of micro-x-ray fluorescence analysis (micro-RFA) with mapping revealed a uniform distribution of selenium on the sorbent surface. The possibility of determining selenium in the sorbent phase by micro-RFA is shown. When comparing the obtained results with the results of calculations by the method of fundamental parameters, it is shown the necessity of using standard samples of sorbates to obtain correct results of RFA determination of selenium in the sorbent phase.

Determination of the composition of binary chalcogenide glasses by X-ray fluorescence analysis

2010 ◽  
Vol 44 (1) ◽  
pp. 24-27 ◽  
Author(s):  
G. A. Bordovsky ◽  
A. V. Marchenko ◽  
P. P. Seregin ◽  
N. N. Smirnova ◽  
E. I. Terukov
Keyword(s):  
Chalcogenide Glasses ◽  
Fluorescence Analysis ◽  
X Ray

Quantitative Determination of some Carbonate Minerals in Greenschist Facies Meta-volcanic Rocks

1972 ◽  
Vol 9 (1) ◽  
pp. 36-42 ◽  
Author(s):  
Calvert C. Bristol
Keyword(s):  
Standard Deviation ◽  
Quantitative Determination ◽  
Volcanic Rocks ◽  
Internal Standard ◽  
Greenschist Facies ◽  
Carbonate Mineral ◽  
Mineral Contents ◽  
X Ray ◽  
Fine Grained

X-ray powder diffraction methods, successful in quantitative determination of silicate minerals in fine-grained rocks, have been applied to the determination of calcite, dolomite, and magnesite in greenschist facies meta-volcanic rocks. Internal standard graphs employing two standards (NaCl and Mo) have been determined.Carbonate mineral modes (calcite and dolomite) for 6 greenschist facies meta-volcanic rocks obtained by the X-ray powder method have been compared to normative carbonate mineral contents calculated for the same rocks. This comparison showed a maximum variation of 7.7 wt.% between the X-ray modes and the normative carbonate mineral contents of the rocks. Maximum standard deviation for the X-ray modes of these rocks was equivalent to 4.4 wt.%.

Total reflection X-ray fluorescence analysis of fly ash from Bulgarian coal-fired power plants

2015 ◽  
Vol 69 (5) ◽  
Author(s):  
Albena K. Detcheva ◽  
Svilen E. Mitsiev ◽  
Paunka S. Vassileva ◽  
Juri H. Jordanov ◽  
Metody G. Karadjov ◽  
...  
Keyword(s):  
Fly Ash ◽  
Power Plants ◽  
Coal Fly Ash ◽  
Internal Standard ◽  
Fluorescence Analysis ◽  
Total Reflection ◽  
X Ray

AbstractThe contents of Cl, Ca, K, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, As, Se, Rb, Sr, Ba and Pb in raw coal fly ash from five Bulgarian power plants were determined by total reflection X-ray fluorescence (TXRF), using gallium as the internal standard. The samples were analysed as in slurry form in Triton

Measurement Of Relative X-Ray Intensity Ratios for Elements With Z=14 to 92 Using EDXRF Spectrometer

1993 ◽  
Vol 37 ◽  
pp. 697-709 ◽  
Author(s):  
Krassimir N. Stoev ◽  
Joseph F. Dlouhy
Keyword(s):  
Fluorescence Analysis ◽  
Radiative Transition ◽  
Published Data ◽  
Emission Rates ◽  
Experimental Physics ◽  
X Ray ◽  
Overlapped Peaks ◽  
Intensity Ratios ◽  
Atomic Structure Calculations

Nowadays x-ray fluorescence analysis is one of the major techniques for determination of trace elements. Vacuum operated Si (Li) .energy-dispersive x-ray spectrometers can analyze simultaneously up to 50 elements from Na (Z=11) to U (Z = 92) . Proper interpretation of the accumulated spectra requires correct solution of x-ray line overlap problems. In many cases knowledge of x-ray intensity ratios can make the procedure for resolving the overlapped peaks more reliable and reproducible. Measurements of radiative transition rates can also provide fundamental tests of theoretical atomic structure calculations. There are many other useful applications of x-ray emission rates in theoretical and experimental physics. On the other hand, there are differences in the published data, which suggests that x-ray intensity ratios are still not known with the necessary accuracy, and new measurements are useful and necessary.

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