Rapid X-Ray Fluorescence Determination of Phosphorus in Geologic Samples

1971 ◽  
Vol 25 (1) ◽  
pp. 41-43 ◽  
Author(s):  
Brent P. Fabbi

Calcium and Kβ1 and Kβ5 both have second order (II) lines that interfere spectrally with the phosphorus Kα1 first order (I) analytical line in the x-ray fluorescence determination. By combining maximum pulse height discrimination with a mathematical correction for peak overlap, phosphorus can be accurately determined in a wide variety of geologic samples.

1971 ◽  
Vol 25 (3) ◽  
pp. 316-318 ◽  
Author(s):  
Brent P. Fabbi

It is possible to accurately determine barium and strontium in a variety of geologic samples by the XRF method proposed herein after correcting for matrix effects. The first-order (I) titanium Kα1 line interferes spectrally with the barium first-order (I) Lα1 analytical line. Iron significantly absorbs the emitted strontium x-ray quanta. Both of these effects were investigated in detail and a method of correcting for them developed. Detection limit for both elements is about 10 ppm.


Nukleonika ◽  
2015 ◽  
Vol 60 (2) ◽  
pp. 263-265
Author(s):  
Ireneusz Książek

Abstract In this note the ratio of the second to the first order reflection is determined for the KAP and PbSt crystals, for wavelengths corresponding to the Al K-line emission. The source of the radiation was a low-voltage stabilized X-ray tube. The X-rays were detected with a Bragg spectrometer equipped with a proportional counter detector. The signal measured by the proportional counter was subsequently pulse height analyzed.


1989 ◽  
Vol 53 (371) ◽  
pp. 357-362 ◽  
Author(s):  
Philip J. Potts ◽  
Andrew G. Tindle

AbstractThe analytical characteristics of a W/Si multilayer dispersion element (MLDE) with a nominal 2d spacing of 60 Å are assessed and compared with those of a conventional thallium acid phthalate (TAP) crystal for the determination of fluorine in silicate and phosphate minerals by electron microprobe. Measured count rates for fluorine were found to be up to fourteen times higher using the MLDE compared with TAP giving improved detection limits of 0.02 to 0.08 wt. % F (six sigma, 100s count time) compared with equivalent data of 0.06 to 0.12 wt. % F by TAP. At equivalent spectrometer angles, peak widths by MLDE were broader by a factor of 2 to 3. However, an important advantage of MLDE was found to be the absence of multiple order diffractions higher than the second order. In consequence, the troublesome third order P-Kα line interference on the F-Kα line, normally encountered in the analysis of apatites, is absent in determinations made using the MLDE. Conversely small interferences on the F-Kα line were detected from the first-order Lα line of Fe and second-order Lα line of Mg. X-ray data and spectra of selected minerals are presented to demonstrate these interferences. Detection limits for elements that can also be determined using the MLDE were 0.07 to 0.15 wt. % oxygen and 0.34 wt. % carbon.


2020 ◽  
Vol 86 (10) ◽  
pp. 18-22
Author(s):  
K. N. Vdovin ◽  
K. G. Pivovarova ◽  
N. A. Feoktistov ◽  
T. B. Ponamareva

Zinc sulfate is the main component in the composition of the acidic zinc plating electrolyte. Deviation in the electrolyte composition from the optimum content leads to destabilization of the electrolysis process and deteriorate the quality of the resulting zinc coating. The proper quality of a zinc coating obtained by galvanic deposition can be ensured only with timely monitoring and adjustment of the electrolyte composition. A technique of X-ray fluorescence determination of zinc (in terms of zinc sulfate) in an acidic zinc plating electrolyte is proposed. The study was carried out using an ARL Quant’X energy dispersive spectrometer (Thermo Fisher Scientific, USA) with a semiconductor silicon-lithium detector. The features of the spectrometer design are presented. The optimal parameters of excitation and detection of zinc radiation were specified when the electrolyte sample was diluted 1:1000. The ZnKα1 line was used as an analytical line. The plotted calibration graph is linear, the correlation coefficient being 0.999234. The results of zinc determination according to the developed method were compared with the data of the reference method of complexometric titration to prove the reliability of the procedure. The results are characterized by good convergence and accuracy. The proposed method of X-ray fluorescence zinc determination in a zinc plating electrolyte equals complexometric titration in the limiting capabilities and even exceeds the latter in terms of the simplicity of sample preparation and rapidity. The developed method of X-ray fluorescence determination of zinc is implemented in analysis of the electrolyte used in the continuous galvanizing unit at «METSERVIS LLC».


2020 ◽  
Vol 56 (14) ◽  
pp. 1423-1430
Author(s):  
V. M. Chubarov ◽  
A. A. Amosova ◽  
A. L. Finkelshtein

2018 ◽  
Vol 144 ◽  
pp. 87-91 ◽  
Author(s):  
Sangita Dhara ◽  
Ajay Khooha ◽  
Ajit Kumar Singh ◽  
M.K. Tiwari ◽  
N.L. Misra

1970 ◽  
Vol 24 (4) ◽  
pp. 426-428 ◽  
Author(s):  
Brent P. Fabbi ◽  
William J. Moore

Determination of total sulfur by x-ray fluorescence eliminates problems of incomplete oxidation of sulfur or coprecipitation often encountered in gravimetric analyses. Durable pellets are prepared from finely ground sample powders mixed with chromatographic cellulose. X-ray fluorescence total sulfur values compare well with gravimetric sulfur values.


2013 ◽  
Vol 56 (9) ◽  
pp. 1088-1091 ◽  
Author(s):  
Yu. V. Antonova ◽  
A. V. Zablotskii ◽  
O. I. Lyamina ◽  
Yu. A. Karpov ◽  
A. Yu. Kuzin ◽  
...  

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