scholarly journals The application of X-ray fluorescence analysis to research the chemical compositions of tea and coffee samples

2019 ◽  
Vol 23 (1) ◽  
pp. 6-23 ◽  
Author(s):  
А. G. Revenko ◽  
◽  
D. S. Sharykina ◽  
Clay Minerals ◽  
2006 ◽  
Vol 41 (3) ◽  
pp. 717-725 ◽  
Author(s):  
S. Battaglia ◽  
L. Leoni ◽  
F. Sartori

AbstractA new method for determining the cation exchange capacity (CEC) of clays is proposed. The method is based on X-ray fluorescence analysis of natural and Ba-exchanged clays following the analytical procedure suggested by Franzini et al. (1975). This procedure, which utilizes powder pellets and is based on a full matrix correction method, is frequently applied in Earth Sciences laboratories for the routine analysis of minerals and rocks. For the analysis of Ba-exchanged clays, Franzini's procedure has been modified slightly to account for the contribution of Ba to matrix effects.The new method, which furnishes both the CEC and the chemical compositions of the whole natural clay samples, has been tested on the eight ‘Source Clays’ of The Clay Minerals Society. The results compare well with data reported in the literature and confirm the accuracy and precision of the method and make it a valid alternative to techniques based on wet chemistry, execution of which is usually more time-consuming and which often requires greater analytical skill.


1974 ◽  
Vol 18 ◽  
pp. 619-631 ◽  
Author(s):  
T. G. Dzubay ◽  
R. O. Nelson

AbstractA procedure is described for making self absorption corrections for x-ray fluorescence analysis of ambient air aerosols which are collected in two size ranges with a dichotomous sampler. Calculations for fine particles are based on the assumption of a uniform layer of accumulated deposit which has an exponentially decreasing depth profile within a membrane filter. Coarse particles are treated as spheres with a log normal mass distribution which is subject to modification by the sampling device. An average attenuation and the associated uncertainty is deduced for coarse particles by considering a wide variety of possible chemical compositions.


2014 ◽  
Vol 782 ◽  
pp. 629-634 ◽  
Author(s):  
Susanne Strobl ◽  
Roland Haubner

At the late second and early third century coin copies, termed subferrata, were produced in the provinces Noricum and Pannonia of the Roman Empire. Subferrata consist of an iron core, which was plated with a copper alloy. To get information about the manufacturing process and the materials used, coins were cut and investigated after metallographic preparation by light optical microscope (LOM). Scanning electron microscopy (SEM) and energy disperse X-ray analysis (EDX) were used to get information about the local chemical compositions. The general composition was determined by X-ray fluorescence analysis (RFA). The Cu alloy coatings consist of Cu, Pb, Sn, Zn and small amounts of Ag. This alloy is a variant of gunmetal, known as leaded red brass. The coatings show mainly differences in the Pb and Sn content and moreover the intermetallic phase Cu41Sn11 was found. Inside the red brass coating droplet-shaped iron inclusions were observed. Near the interface, between coating and iron core, Cu and Pb were detected at the grain boundaries (liquid metal embrittlement). Probably, the iron flan was plated by immersing in a molten copper alloy. In the ferritic-pearlitic iron core, slag inclusions and regions with various carbon contents were observed. Furthermore, deformation twins (Neumann lines) were found in the Fe core ́s microstructure, leading to the suggestion that coining was performed after cooling the flan.


Materials ◽  
2019 ◽  
Vol 12 (21) ◽  
pp. 3578 ◽  
Author(s):  
Anatoly Kovalev ◽  
Dmitry Wainstein ◽  
Vladimir Vakhrushev ◽  
Anton Volkov ◽  
Ulyana Kologrieva

Metallurgical vanadium-containing converter slag could be used as an alternative vanadium source. The development of a physico-chemical basis for the comprehensive processing of industrial vanadium-containing debris requires information about their elemental composition as well as the oxidation degrees of the elements and forms of compounds in order to solve two key problems: a better utilization of industrial wastes and a lowering of environment impact. This research was aimed at the development of methods to determine the fractions of elements and their oxidation degrees in vanadium-containing industrial debris exemplified by basic oxygen converter vanadium slags. A set of bulk and surface analysis methods (X-ray fluorescence analysis (XRF), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS)) was used for this purpose: based on results of elemental analysis, SEM detects the oxide phases of metals, while an analysis of the XPS lines’ fine structures provides fractions of corresponding elements with definite oxidation degrees. In this way, one can determine the fractions of vanadium in multiple oxidation degrees in slags and can properly select the chemicals and parameters of chemical processes for its fullest extraction.


Author(s):  
D. A. Carpenter ◽  
M. A. Taylor

The development of intense sources of x rays has led to renewed interest in the use of microbeams of x rays in x-ray fluorescence analysis. Sparks pointed out that the use of x rays as a probe offered the advantages of high sensitivity, low detection limits, low beam damage, and large penetration depths with minimal specimen preparation or perturbation. In addition, the option of air operation provided special advantages for examination of hydrated systems or for nondestructive microanalysis of large specimens.The disadvantages of synchrotron sources prompted the development of laboratory-based instrumentation with various schemes to maximize the beam flux while maintaining small point-to-point resolution. Nichols and Ryon developed a microprobe using a rotating anode source and a modified microdiffractometer. Cross and Wherry showed that by close-coupling the x-ray source, specimen, and detector, good intensities could be obtained for beam sizes between 30 and 100μm. More importantly, both groups combined specimen scanning with modern imaging techniques for rapid element mapping.


Author(s):  
D. A. Carpenter ◽  
Ning Gao ◽  
G. J. Havrilla

A monolithic, polycapillary, x-ray optic was adapted to a laboratory-based x-ray microprobe to evaluate the potential of the optic for x-ray micro fluorescence analysis. The polycapillary was capable of collecting x-rays over a 6 degree angle from a point source and focusing them to a spot approximately 40 µm diameter. The high intensities expected from this capillary should be useful for determining and mapping minor to trace elements in materials. Fig. 1 shows a sketch of the capillary with important dimensions.The microprobe had previously been used with straight and with tapered monocapillaries. Alignment of the monocapillaries with the focal spot was accomplished by electromagnetically scanning the focal spot over the beveled anode. With the polycapillary it was also necessary to manually adjust the distance between the focal spot and the polycapillary.The focal distance and focal spot diameter of the polycapillary were determined from a series of edge scans.


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.


Sign in / Sign up

Export Citation Format

Share Document