A Study of X-Ray Fluorescence Method with Vacuum and Air-Path Spectrographs for the Determination of Film Thicknesses of II-VI Compounds

1967 ◽  
Vol 11 ◽  
pp. 191-203
Author(s):  
Frank L. Chan
Keyword(s):  
Energy Conversion ◽  
Vacuum Chamber ◽  
Fluorescence Method ◽  
Chemical Methods ◽  
X Ray ◽  
Aerospace Application ◽  
Physical And Chemical ◽  
Orange Color

AbstractFilms of II-VI compounds have been prepared by vacuum technique for the determination of their thicknesses. Some difficulties have been experienced in preparing good quality films- The positron of the substrate in the vacuum chamber, the rate of deposition, and the temperature of sublimation are some of the factors influencing the quality of these films. For instance, films of cadmium sulfide could be prepared in the usual yellow or orange color or in colors ranging from brown to black, depending on the conditions enumerated. For energy conversion, a film of proper thickness is one of the requirements for aerospace application. Among the various methods used for the determination of the thickness of these films, X-ray fluorescence can be performed rapidly and nondestructively. After determination of thickness by the X-ray fluorescence method, the samples can be used for other determinations and for energy conversion without their efficiency's having been affected. Other physical and chemical methods have been worked out. Comparison of these methods with the X-ray fluorescence method is made. Procedures and results are presented.

Sem and X-Ray Analysis of Renal and Biliary Calculi

1976 ◽  
Vol 34 ◽  
pp. 306-307
Author(s):  
R. J. Narconis ◽  
G. L. Johnson
Keyword(s):  
Chemical Constituents ◽  
Natural State ◽  
X Ray Diffraction ◽  
Chemical Methods ◽  
X Ray ◽  
Additional Dimension ◽  
Biliary Calculi ◽  
Calculus Formation ◽  
Scanning Electron

Analysis of the constituents of renal and biliary calculi may be of help in the management of patients with calculous disease. Several methods of analysis are available for identifying these constituents. Most common are chemical methods, optical crystallography, x-ray diffraction, and infrared spectroscopy. The application of a SEM with x-ray analysis capabilities should be considered as an additional alternative.A scanning electron microscope equipped with an x-ray “mapping” attachment offers an additional dimension in its ability to locate elemental constituents geographically, and thus, provide a clue in determination of possible metabolic etiology in calculus formation. The ability of this method to give an undisturbed view of adjacent layers of elements in their natural state is of advantage in determining the sequence of formation of subsequent layers of chemical constituents.

X-ray fluorescence determination of zinc sulfate in acidic zinc plating electrolyte

2020 ◽  
Vol 86 (10) ◽  
pp. 18-22
Author(s):  
K. N. Vdovin ◽  
K. G. Pivovarova ◽  
N. A. Feoktistov ◽  
T. B. Ponamareva
Keyword(s):  
Zinc Sulfate ◽  
Zinc Coating ◽  
Electrolyte Composition ◽  
Complexometric Titration ◽  
X Ray ◽  
Fluorescence Determination ◽  
Zinc Plating ◽  
Zinc Determination

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».

scholarly journals SPECTROSCOPIC METHODS TO DETERMINATION OF GEOTHITE IN KAOLINITE

2020 ◽  
Vol 17 (35) ◽  
pp. 303-314
Author(s):  
Marcelo Kehl; ; ; ; DE SOUZA ◽  
Marcos Antônio KLUNK ◽  
Soyane Juceli Siqueira XAVIER ◽  
Mohuli DAS ◽  
Sudipta DASGUPTA
Keyword(s):  
Spectroscopic Methods ◽  
Industrial Minerals ◽  
X Ray Diffraction ◽  
Simple Shape ◽  
X Ray ◽  
Spectroscopic Monitoring ◽  
Partial Release ◽  
Primary Minerals

One of the main contaminants of kaolinite, the iron, directly impacts quality in its commercial value. The spectroscopic monitoring, measured the depth of absorption of kaolinite, is compared with the literature in order to identify possible contaminants. The occurrence of kaolinite is due to the formation of primary minerals after the partial release of cations and silicon. This clay-mineral has a simple shape, with variable crystallographic imperfections, especially in the presence of iron, which replaces aluminum in the mineral chain, causing various structural disorganizations. The extraction of industrial minerals combined with geological studies, allows the development of new sources of energy, such as clay minerals, in particular kaolinite. Depending on the origin of the kaolinites, the presence of iron oxides in its structure, Fe2O3 and FeO(OH), are common. By comparing the results of spectroscopy (X-ray fluorescence, X-ray diffraction, RAMAN) and imaging using SEM-EDS, it was possible to identify kaolinite, with a higher determination coefficient, when the proportion of kaolinite reaches 60% or more in the mix. Kaolinite can be identified and quantified with a high correlation in the mixture from the sample absorption. Thus, the method has great potential to assist in quantifying and, consequently, in discriminating the quality of kaolinite.

scholarly journals Medidas de adesão entre agregado e ligante asfáltico

TRANSPORTES ◽  
2008 ◽  
Vol 16 (1) ◽  
Author(s):  
Kamilla Lima Vasconcelos ◽  
Amit Bhasin ◽  
Dallas N. Little ◽  
Jorge Barbosa Soares
Keyword(s):  
Chemical Interaction ◽  
Asphalt Binder ◽  
Fatigue Cracking ◽  
Adhesion Measurement ◽  
Materials Used ◽  
Enthalpy Of Immersion ◽  
Physical And Chemical ◽  
Energy Components

<p>A adesão entre agregado e ligante asfáltico vem sendo apontada como uma propriedade de grande importância para a causa de defeitos encontrados em pavimentos asfálticos, tais como trincas por fadiga, e dano por umidade. Diferentes mecanismos existem na literatura para explicar a adesão entre os dois materiais, porém, estes mecanismos podem ser resumidos em três grandes grupos: inter- travamento mecânico, adesão física, e interação química. A ocorrência de mais de um mecanismo simultaneamente parece ser o fenô- meno mais provável, sendo a relevância de cada um dependente das características físicas e químicas do agregado e do ligante asfálti- co. No presente trabalho, dois procedimentos foram utilizados para acessar a adesão entre agregado e ligante. O primeiro constou do cálculo do trabalho de adesão através da energia livre de superfície dos materiais envolvidos e o segundo, da determinação da entalpia de imersão quando soluções de asfalto são postas em contato com o agregado. Todos os materiais usados foram provenientes da biblio- teca de referência do SHRP sendo um pedregulho como agregado, e três diferentes ligantes asfálticos. Os resultados mostraram a capa- cidade do microcalorímetro em detectar possíveis interações químicas na adesão entre agregado e ligante asfáltico, em conjunto com adesão física. A presença de grupos funcionais mais fortemente adsorvidos pela superfície dos agregados justificou os maiores valores de entalpia de imersão para as combinações onde esses grupos se encontravam presentes.</p><p><em><strong>Abstract</strong> Adhesion between the asphalt binder and the aggregate is critical to the performance and durability of asphalt mixtures. According to the literature, distresses mechanisms such as fatigue cracking and moisture induced damage are correlated to the nature and quality of adhesion between these two materials. Different mechanisms already exist to explain adhesion, but they can be summa- rized in three main groups: mechanical interlocking, physical adhesion and chemical interaction. Although discussions of isolated theo- ries and mechanisms help to clarify the understanding of adhesion, they can rarely be separated completely to each other. The physical and chemical characteristics of asphalt and aggregate will in fact determine the relevance of each of these mechanisms. This study presents the results of two procedures for adhesion measurement: (i) an indirect method based on the surface free energy components of asphalt binder and aggregate; and (ii) the determination of the enthalpy of immersion through the use of a microcalorimeter. The materials used, a gravel as aggregate and three different neat asphalts, were provided by the Strategic Highway Research Program's Material Reference Library. The results showed the capacity of the microcalorimeter in detecting possible chemical reactions together with physical adhesion. The presence of functional groups more strongly adsorbed by the aggregate surface justified the higher values of the heat of immersion. </em></p>

Medical Image Enhancement Using Edge Information-Based Methods

2017 ◽  
pp. 123-148
Author(s):  
S. Anand
Keyword(s):  
Image Enhancement ◽  
Medical Image ◽  
Hyperbolic Function ◽  
Edge Information ◽  
X Ray ◽  
Enhancement Method ◽  
Chest X Ray ◽  
Medical Image Enhancement

Medical image enhancement improves the quality and facilitates diagnosis. This chapter investigates three methods of medical image enhancement by exploiting useful edge information. Since edges have higher perceptual importance, the edge information based enhancement process is always of interest. But determination of edge information is not an easy job. The edge information is obtained from various approaches such as differential hyperbolic function, Haar filters and morphological functions. The effectively determined edge information is used for enhancement process. The retinal image enhancement method given in this chapter improves the visual quality of the vessels in the optic region. X-ray image enhancement method presented here is to increase the visibility of the bones. These algorithms are used to enhance the computer tomography, chest x-ray, retinal, and mammogram images. These images are obtained from standard datasets and experimented. The performance of these enhancement methods are quantitatively evaluated.

scholarly journals Evaluation of mineral fiber properties using x-ray fluorescence analysis and measurement of natural radioactivity

2018 ◽  
Vol 170 ◽  
pp. 03018 ◽  
Author(s):  
Andrey Medvedev ◽  
Ekaterina Bobrova ◽  
Alexey Poserenin ◽  
Ervand Zarmanyan
Keyword(s):  
Fluorescence Analysis ◽  
Mineral Wool ◽  
Factors Affecting ◽  
Mineral Fibers ◽  
X Ray ◽  
Fiber Properties ◽  
Building Systems ◽  
Heavy Metal Oxides

The article analyzes the factors affecting the longevity of insu-lating systems and the operational resistance of products based on mineral fibers. It is emphasized that the ratio of acid oxides contained in the charge to the main oxides is the main factor influencing the operational resistance of mineral fibers, as well as the energy intensity of their production. A hy-pothesis has been put forward and confirmed that the operational resistance of a fiber depends on the content of heavy metals (their oxides) in the ini-tial charge. Determination of the elemental composition of stone wool samples was carried out by X-ray fluorescence analysis. Conducted sam-ples with a different acidity module of the study, show, that the fibers are safe by radiation indices, and their operational resistance can be affected by heavy metal oxides. It is substantiated that the durability of building systems in which mineral wool products are used as thermal insulation is determined by the properties of mineral wool products, the literacy of de-sign solutions and the quality of installation. The properties of mineral wool products, including their operational resistance, depend on the prop-erties of mineral fibers and the observance of technological regimes both on the fact of the most complete curing of the binder and on the features of formation of the volume-oriented structure of the mineral wool carpet.

A Rapid and Accurate X-Ray Determination of the Rare Earths Elements in Solid or Liquid Materials using the Double Dilution Method

1968 ◽  
Vol 12 ◽  
pp. 546-562
Author(s):  
R. Tertian
Keyword(s):  
Rare Earth ◽  
Rare Earth Elements ◽  
Accurate Determination ◽  
Fluorescence Analysis ◽  
Dilution Method ◽  
Practical Advantage ◽  
X Ray ◽  
The Matrix

AbstractThe double dilution method has many important advantages. For any element to be determined, let us say A, It enables us to control or calculate the matrix factor (sum of the absorption end enhancement effects) for the sample being Investigated towards A radiation, and it furnishes corrected Intensities which are strictly proportional to A concentration. Thus the results are exact, whatever the general composition of the sample, their accuracy depending only on the quality of measurement and preparation. Another major practical advantage is that the method does not require systematic calibration but only a few permanent standards consisting of a pure compound or of an accurately known sample.The procedure has been tested successfully for accurate determination of rare earth elements using, for solid materials such as ores and oxide mixtures, the borax fusion technique. It also can be readily applied to liquids. All the rare earth elements can be titrated by that method, as well as yttrium, thorium and, if necessary, all the elements relevant to X-ray fluorescence analysis. The concentration range considered for solids is of one comprised between 0.5 and 100 % and, with a lesser accuracy, between 0.1 and 0-5 % Examples are given relative to the analysis of various ores. Finally it rcust be pointed out that the method is universal and applies to the analysis of every solid, especially ores, provided that they can be converted to solid or liquid solutions. It appears that most industrial analyses can be worked on In this way.

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