X-Ray Fluorescence Analysis of Stainless Steel in Aqueous Solutions

1959 ◽  
Vol 31 (10) ◽  
pp. 1629-1631 ◽  
Author(s):  
R. W. Jones ◽  
R. W. Ashley
2020 ◽  
pp. 47-56
Author(s):  
Yelena Vladimirovna Stolpovskaya ◽  
Natalya Nikolaevna Trofimova ◽  
Vasily Anatolyevich Babkin ◽  
Spartak Spiridonovich Khutsishvili ◽  
Roman Georgievich Zhitov ◽  
...  

The purpose of this work was to study and optimize the complexation reaction of Mn2+ ions with flavonoid dihydroquercetin (DHQ) in aqueous solutions. It was found that the interaction of DHQ (0.015–0.030 M) with manganese (II) salts at molar ratios of DHQ : Mn2+ from 1 : 1 to 1 : 3 at pH 6.9–7.9 leads to the formation of a complex compound (CC) with a stoichiometric ratio of metal : flavonoid ligand (Met : L) 1 : 1. The conditions for the complexation of Mn2+ ions with dihydroquercetin at laboratory conditions optimized for the yield of the product, are proposed. The maximum yield of the complex (95%) was achieved at the interaction of DHQ with Mn(CH3COO)2∙4H2O under conditions: pH 7.7, 70 °C, the reaction time was 15 min, the molar ratio of the initial reagents DHQ: Mn2+ was 1 : 1.5, the initial concentrations were 0.020 M DHQ and 0.030 M Mn2+. The most probable composition of the complex with the determination of the amount of bound water [MnL(OH)(H2O)2] and the structure of the complex were established using the data of thermogravimetry (TG), differential scanning calorimetry (DSC), elemental analysis and X-ray fluorescence analysis (XRF), confirmed by the data of total reflection X-ray fluorescence analysis (TXRF), and EPR spectroscopy data.


1970 ◽  
Vol 14 ◽  
pp. 78-91
Author(s):  
G.E. Hicho ◽  
H. Yakowitz ◽  
S.D. Rasberry ◽  
R.E. Michaelis

AbstractThis standard was produced by powder metallurgical techniques using known amounts of austenite. Using these techniques, 134 specimens were prepared. Because these standards are expected to be used primarily for the calibration of X-ray diffraction equipment, only one surface of each standard is certified, and these surfaces range from 3.1 percent to 5.2 percent in austenite content. To make the specimens, 310 stainless steel powder (austenitid) was blended with 430 stainless steel powder (ferritic) to make a mixture of 5 percent austenite in ferrite. The material was compacted, sintered, polished and etched so the austenite appears white and the ferrite, a deep brown. Then quantitative microscopy methods were used to determine the percentage of austenite near the surface. Furthers more, the 310 powder contains 20 percent of nickel while the 430 powder contains virtually no nickel. Therefore, after establishing a meaningful calibration curve, X-ray fluorescence analysis for the nickel content was also used as a direct measurement of the amount of retained austenite on the surface of the compact. Both procedures were carried out on fifteen specimens statistically selected from the total number of compacts produced. Agreement, within experimental error limits, was obtained between the X-ray fluorescence results and quantitative microscopy results. The X-ray fluorescence method was used to characterize all additional compacts. X-ray diffraction determinations of austenite content are in good agreement with the X-ray fluorescence and quantitative microscopy results. The compacts may be used as X-ray diffraction standards for austenite or in special cases as X-ray fluorescence standards for nickel content.


1973 ◽  
Vol 27 (5) ◽  
pp. 352-355 ◽  
Author(s):  
D. L. Taylor ◽  
G. Andermann

The “degree of internal standardization” for the scattered radiation method of compensation for matrix effects in x-ray fluorescence analysis is defined as the closeness of agreement between the results of analyses of specimens containing identical concentrations of analyte but with differing over-all elemental constituencies. The definition is derived in mathematical terms and is applied to experimental data of analyses of calcium in aqueous solutions containing different dissolved substances as matrix variants. The matrix compensation effectiveness of various wavelengths of scattered radiation can be clearly indicated. Interpretation of the results in terms of basic spectroscopic parameters is offered.


Author(s):  
Anastasiya Kutuzova ◽  
Tetiana Dontsova ◽  
Maryna Davydova

Antibiotics have been found in water bodies of different origin around the world, including natural waters. The presence of antibiotics in natural waters is already an important environmental problem, as they pose a potential threat to the environment. Analysis of the literature shows that photocatalytic methods are considered to be more promising than biological methods and adsorption processes for the treatment of water bodies contaminated with antibiotics and other pharmaceuticals. The aim of this study was to determine the efficiency of antibiotics removal (ciprofloxacin, sulfamethoxazole and trimethoprim) by photocatalytic methods over TiO2 photocatalyst modified with yttrium oxide. For this purpose, a commercial sample of TiO2 P25 (Evonik) was modified, which was further characterized by X-ray diffraction and X-ray fluorescence analysis methods. The obtained data indicate the presence of yttrium in commercial P25 sample after modification. Studies on the removal of antibiotics from aqueous solutions by photocatalytic methods were carried out in three ways: employing modified photocatalyst; combination of photocatalyst and hydrogen peroxide, and the combination of photocatalyst with hydrogen peroxide and ozone. The results of research demonstrate high efficiency of photocatalytic methods in the oxidation of antibiotics in aqueous solutions, among which the greatest oxidation is achieved using the combination of heterogeneous photocatalyst, hydrogen peroxide and ozone.


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.


2007 ◽  
Vol 2007 (suppl_26) ◽  
pp. 61-66 ◽  
Author(s):  
B. Peplinski ◽  
B. Adamczyk ◽  
G. Kley ◽  
K. Adam ◽  
F. Emmerling ◽  
...  

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