Chemical composition of metapelitic chlorites: X-ray diffraction and optical property approach

1997 ◽  
Vol 9 (4) ◽  
pp. 829-842 ◽  
Author(s):  
Fernando Nieto
2010 ◽  
Vol 93-94 ◽  
pp. 231-234
Author(s):  
B. Hongthong ◽  
Satreerat K. Hodak ◽  
Sukkaneste Tungasmita

Strontium substituted hydroxyapatite(SrHAp) were fabricated both in the form of powder as reference and thin film by using inorganic precursor reaction. The sol-gel process has been used for the deposition of SrHAp layer on stainless steal 316L substrate by spin coating technique, after that the films were annealed in air at various temperatures. The chemical composition of SrHAp is represented (SrxCa1-x)5(PO4)3OH, where x is equal to 0, 0.5 and 1.0. Investigations of the phase structure of SrHAp were carried out by using X-ray diffraction technique (XRD). The results showed that strontium is incorporated into hydroxyapatite where its substitution for calcium increases in the lattice parameters, and Sr3(PO4)2 can be detected at 900°C. The SEM micrographs showed that SrHAp films exhibited porous structure before develop to a cross-linking structure.


2017 ◽  
Vol 17 (2) ◽  
pp. 107-110
Author(s):  
K. Stec ◽  
J. Podwórny ◽  
B. Psiuk ◽  
Ł. Kozakiewicz

Abstract Using the available analytical methods, including the determination of chemical composition using wavelength-dispersive X-ray fluorescent spectroscopy technique and phase composition determined using X-ray diffraction, microstructural observations in a highresolution scanning microscope equipped with an X-ray microanalysis system as well as determination of characteristic softening and sintering temperatures using high-temperature microscope, the properties of particular chromite sands were defined. For the study has been typed reference sand with chemical properties, physical and thermal, treated as standard, and the sands of the regeneration process and the grinding process. Using these kinds of sand in foundries resulted in the occurrence of the phenomenon of the molding mass sintering. Impurities were identified and causes of sintering of a moulding sand based on chromite sand were characterized. Next, research methods enabling a quick evaluation of chromite sand suitability for use in the preparation of moulding sands were selected.


1991 ◽  
Vol 05 (21) ◽  
pp. 1447-1456 ◽  
Author(s):  
A. R. HARUTUNYAN ◽  
L. S. GRIGORYAN ◽  
A. S. KUZANYAN ◽  
A. A. KUZNETSOV ◽  
A. A. TERENTIEV ◽  
...  

Two samples of benzene-treated Bi–Pb–Sr–Ca–Cu–O powder exhibited at 300 K magnetic field dependent diamagnetism and magnetization irreversibility. The treatment with benzene resulted also in the appearance of microwave absorption at low magnetic fields, while is sensitive to magnetic history of the sample. From X-ray diffraction data one can see that upon benzene treatment the reflections of 85 K and 110 K phases do not change practically, but a series of new reflections appeared, indicating a lattice modulation with 4.9 nm periodicity. A microprobe analysis revealed substantial inhomogeneity of chemical composition across the samples. The room temperature anomalies were weakened in one sample and vanished in the second upon thermal cycling.


2012 ◽  
Vol 488-489 ◽  
pp. 76-81 ◽  
Author(s):  
Subramani Shanmugan ◽  
Mutharasu Devarajan ◽  
Kamarulazizi Ibrahim

Sb layered Te/Cd thin films have been prepared by using Stacked Elemental Layer (SEL) method. The presence of mixed phases (CdTe and Sb2Te3) in the films was confirmed by the x-ray diffraction technique. The calculated structural parameters demonstrated the feasibility of Sb doping via SEL method. The topographical and electrical studies of the synthesized thin films depicted the influence of Sb on both surface morphology and conductivity. The values of conductivity of the annealed films were in between 2 x 10-3 and 175 x 10-2 Scm-2. A desired chemical composition of films was confirmed from spectrum shape analysis using energy dispersive x-ray.


Author(s):  
H. Catherine W. Skinner ◽  
Malcolm Ross ◽  
Clifford Frondel

A mineral is a naturally occurring, crystalline inorganic compound with a specific chemical composition and crystal structure. Minerals are commonly named to honor a person, to indicate the geographic area where the mineral was discovered, or to highlight some distinctive chemical, crystallographic, or physical characteristic of the substance. Each mineral sample has some obvious properties: color, shape, texture, and perhaps odor or taste. However, to determine the precise composition and crystal structure necessary to accurately identify the species, one or several of the following techniques must be employed: optical, x-ray diffraction, transmission electron microscopy and diffraction, and chemical and spectral analyses. The long history of bestowing names on minerals has provided some confusing legacies. Many mineral names end with the suffix “ite,” although not most of the common species; no standard naming practice has ever been adopted. Occasionally different names have been applied to samples of the same mineral that differ only in color or shape, but are identical to each other in chemical composition and crystal structure. These names, usually of the common rock-forming minerals, are often encountered and are therefore accepted as synonyms or as varieties of bona fide mineral species. The Fibrous Minerals list (Appendix 1) includes synonyms. A formal description of a mineral presents all the physical and chemical properties of the species. In particular, distinctive attributes that might facilitate identification are noted, and usually a chemical analysis of the first or “type” specimen on which the name was originally bestowed is included. As an example, the complete description of the mineral brucite (Mg(OH)2), as it appears in Dana’s System of Mineralogy, is presented as Appendix 3. Note the complexity of this chemically simple species and the range of information available. In the section on Habit (meaning shape or morphology) both acicular and fibrous forms are noted. The fibrous variety, which has the same composition as brucite, is commonly encountered (see Fig. 1.1D) and is known by a separate name, “nemalite.” Tables to assist in the systematic determination of a mineral species are usually based on quantitative measurements of optical properties (using either transmitted or reflected light, as appropriate) or on x-ray diffraction data.


1990 ◽  
Vol 34 ◽  
pp. 325-335 ◽  
Author(s):  
Steve J. Chipera ◽  
David L. Bish

AbstractThe mass absorption coefficient is a useful parameter for quantitative characterization of materials. If the chemical composition of a sample is known, the mass absorption coefficient can be calculated directly. However, the mass absorption coefficient must be determined empirically if the chemical composition is unknown. Traditional methods for determining the mass absorption coefficient involve measuring the transmission of monochromatic X-rays through a sample of known thickness and density. Reynolds (1963,1967), however, proposed a method for determining the mass absorption coefficient by measuring the Compton or inelastic X-ray scattering from a sample using Mo radiation on an X-ray fluorescence spectrometer (XRF). With the recent advances in solid-state detectors/electronics for use with conventional powder diffractometers, it is now possible to readily determine mass absorption coefficients during routine X-ray diffraction (XRD) analyses.Using Cu Kα radiation and Reynolds’ method on a Siemens D-500 diffractometer fitted with a Kevex Si(Li) solid-state detector, we have measured the mass absorption coefficients of a suite of minerals and pure chemical compounds ranging in μ/ρ from graphite to Fe-metal (μ/ρ = 4.6-308 using Cu Kα radiation) to ±4.0% (lσ). The relationship between the known mass absorption coefficient and the inverse count rate is linear with a correlation coefficient of 0.997. Using mass absorption coefficients, phase abundances can be determined during quantitative XRD analysis without requiring the use of an internal standard, even when an amorphous component is present.


Materials ◽  
2020 ◽  
Vol 13 (14) ◽  
pp. 3082 ◽  
Author(s):  
Bogdan Istrate ◽  
Corneliu Munteanu ◽  
Stefan Lupescu ◽  
Romeu Chelariu ◽  
Maria Daniela Vlad ◽  
...  

In recent years, biodegradable Mg-based materials have been increasingly studied to be used in the medical industry and beyond. A way to improve biodegradability rate in sync with the healing process of the natural human bone is to alloy Mg with other biocompatible elements. The aim of this research was to improve biodegradability rate and biocompatibility of Mg-0.5Ca alloy through addition of Y in 0.5/1.0/1.5/2.0/3.0wt.%. To characterize the chemical composition and microstructure of experimental Mg alloys, scanning electron microscopy (SEM), energy-dispersive spectroscopy (EDS), light microscopy (LM), and X-ray diffraction (XRD) were used. The linear polarization resistance (LPR) method was used to calculate corrosion rate as a measure of biodegradability rate. The cytocompatibility was evaluated by MTT assay (3-(4,5-dimethylthiazole-2-yl)-2,5-diphenyltetrazolium bromide) and fluorescence microscopy. Depending on chemical composition, the dendritic α-Mg solid solution, as well as lamellar Mg2Ca and Mg24Y5 intermetallic compounds were found. The lower biodegradability rates were found for Mg-0.5Ca-2.0Y and Mg-0.5Ca-3.0Y which have correlated with values of cell viability. The addition of 2–3 wt.%Y in the Mg-0.5Ca alloy improved both the biodegradability rate and cytocompatibility behavior.


Materials ◽  
2019 ◽  
Vol 12 (12) ◽  
pp. 2019 ◽  
Author(s):  
Jorge Osio-Norgaard ◽  
Wil V. Srubar

This work presents experimental evidence that confirms the potential for two specific zeolites, namely chabazite and faujasite (with a cage size ~2–13 Å), to adsorb small amounts of chloride from a synthetic alkali-activated cement (AAC) pore solution. Four synthetic zeolites were first exposed to a chlorinated AAC pore solution, two faujasite zeolites (i.e., FAU, X-13), chabazite (i.e., SSZ-13), and sodium-stabilized mordenite (i.e., Na-Mordenite). The mineralogy and chemical composition were subsequently investigated via X-ray diffraction (XRD) and both energy- and wavelength-dispersive X-ray spectroscopy (WDS), respectively. Upon exposure to a chlorinated AAC pore solution, FAU and SSZ-13 displayed changes to their diffraction patterns (i.e., peak shifting and broadening), characteristic of ion entrapment within zeolitic aluminosilicate frameworks. Elemental mapping with WDS confirmed the presence of small amounts of elemental chlorine. Results indicate that the chloride-bearing capacity of zeolites is likely dependent on both microstructural features (e.g., cage sizes) and chemical composition.


Crystals ◽  
2019 ◽  
Vol 9 (7) ◽  
pp. 340 ◽  
Author(s):  
Oswaldo Sánchez-Dena ◽  
Carlos J. Villagómez ◽  
César D. Fierro-Ruíz ◽  
Artemio S. Padilla-Robles ◽  
Rurik Farías ◽  
...  

Existent methods for determining the composition of lithium niobate single crystals are mainly based on their variations due to changes in their electronic structure, which accounts for the fact that most of these methods rely on experimental techniques using light as the probe. Nevertheless, these methods used for single crystals fail in accurately predicting the chemical composition of lithium niobate powders due to strong scattering effects and randomness. In this work, an innovative method for determining the chemical composition of lithium niobate powders, based mainly on the probing of secondary thermodynamic phases by X-ray diffraction analysis and structure refinement, is employed. Its validation is supported by the characterization of several samples synthesized by the standard and inexpensive method of mechanosynthesis. Furthermore, new linear equations are proposed to accurately describe and determine the chemical composition of this type of powdered material. The composition can now be determined by using any of four standard characterization techniques: X-Ray Diffraction (XRD), Raman Spectroscopy (RS), UV-vis Diffuse Reflectance (DR), and Differential Thermal Analysis (DTA). In the case of the existence of a previous equivalent description for single crystals, a brief analysis of the literature is made.


1982 ◽  
Vol 18 ◽  
Author(s):  
R. J. Schutz

The effectiveness of a thin (360Å) layer of reactively sputtered TiN as a diffusion barrier between aluminum and two silicides (PtSi and CoSi2) was evaluated. The chemical composition, structural phases and electrical properties of silicide/Al and silicide/TiN/Al contacts to n-type silicon were studied by Rutherford backscattering spectroscopy, glancing angle X-ray diffraction and Schottky barrier height measurements respectively. The results show that TiN is an effective barrier in these two systems up to at least 450°C, the typical temperature at which aluminum contacts are sintered.


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