X-Ray Fluorescence Determination of Chlorine in Standard Silicate Rocks

1972 ◽  
Vol 26 (2) ◽  
pp. 293-295 ◽  
Author(s):  
Brent P. Fabbi ◽  
Laureano F. Espos

Chlorine has been determined in seventeen international silicate rock standards by x-ray fluorescence analysis, yielding values which compare well with published values. The detection limit for the method is about 10 ppm. Sources of chlorine contamination are considered.

2020 ◽  
Vol 24 (4) ◽  
pp. 236-276
Author(s):  
A. G. Revenko ◽  

X-ray fluorescence analysis (XRF) is widely used when determining the concentrations of elements in various materials in biological research. Current review considers the achievements related to the features of the XRF method. X-ray fluorescence analysis in most cases is a non-destructive method that has proven its potential for measuring the concentrations of elements with a high atomic number Z in organs and tissues in vivo. The main areas of its application in biology and medicine are content determination of basic and toxic elements in plants, samples of bones, teeth, hairs, nails and tissues of vital organs, body fluids such as blood, serum, plasma, saliva, urine, etc. Usually, these studies are part of applied programs that include environmental and metabolic analyses of the population, including the influence of professional factors. The advantages of XRF are also discussed with regards to biological materials. It is noted that the form of the element in the sample practically does not affect the analysis result. In recent years, several new XRF spectrometers models have been designed, where polycapillary lenses and half lenses are used as collimating systems. This is important in the case of in vivo application of X-ray fluorescence determination of certain elements in bones and tissues. The dynamic development is typical for detectors with thermoelectric cooling. Variants of preparation of biological materials for analysis are discussed (grinding, dry or wet ashing, acid decomposition, use of suspensions in the case of XRF with TIR). The results of evaluating the interelement effects for XRF of materials of plant origin, including herbs, spices, apple leaves, birch and tomato leaves, tea, wheat, rye, rice, oatmeal, flax flour, beans, ground, and instant coffee are presented. Examples of the use of XRF in various types of forensic research are considered: poisoning, counterfeiting of drugs and food brands, dental implants, identification of remains. The review presents examples of the participation of Russian X-ray physicists in solving the problems under consideration. The list of references is 400 papers, mainly including the publications of the last 20 years.


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.


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 ◽  
...  

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.


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

2010 ◽  
Vol 44 (1) ◽  
pp. 24-27 ◽  
Author(s):  
G. A. Bordovsky ◽  
A. V. Marchenko ◽  
P. P. Seregin ◽  
N. N. Smirnova ◽  
E. I. Terukov

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