scholarly journals Kinetics of the Thermal Decomposition of Rhodochrosite

Minerals ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 34
Author(s):  
Iván A. Reyes ◽  
Mizraim Flores ◽  
Elia G. Palacios ◽  
Hernán Islas ◽  
Julio C. Juárez ◽  
...  
Keyword(s):  
Thermal Decomposition ◽  
Mass Loss ◽  
Manganese Oxides ◽  
Absorption Spectrometry ◽  
X Ray Diffraction ◽  
X Ray ◽  
Decomposition Reactions ◽  
Mass Losses ◽  
Rate Controlled ◽  
Kinetics Of

Manganese is a widely used element in the steel industry; its main source is a mineral named rhodochrosite (MnCO3). For industrial usage, rhodochrosite is reduced to different manganese oxides by means of nodulation furnaces. In this study, rhodochrosite was thermally analyzed at temperatures ranging from 100 °C to 1200 °C. XRD (Powder X-ray diffraction), XRF (X-ray fluorescence), AAS (Atomic Absorption Spectrometry), and FESEM-EDX (Field Emission Scanning Electron Microscopy-Energy Dispersive X-Ray Spectrometry) were used to characterize the mineral and the residues were analyzed by XRD and FTIR (Fourier-transform infrared spectroscopy) to determine the stoichiometry of the thermal decomposition reactions. Three mass losses were observed, the first attributed to the transformation from carbonate to manganese (III) oxide, the second to the reduction to manganese tetroxide, and the third to the decomposition of calcium carbonate (CaCO3) present as a contaminant in the studied mineral. Thermal decomposition kinetics shows that the first mass loss required 17.91 kJ mol−1, indicating a control by mass transport-controlled process. For the second and third mass loss, the apparent activation energy of 112.41 kJ mol−1 and 64.69 kJ mol−1 was obtained respectively, indicating that both mass loss events were rate-controlled.

Thermal Decomposition Kinetics of Ammonium Aluminum Carbonate Hydroxide

2008 ◽  
Vol 368-372 ◽  
pp. 1577-1579
Author(s):  
Hai Jun Zhang ◽  
En Xia Xiu ◽  
Xiu Juan Wang ◽  
Quan Li Jia ◽  
Hong Wei Sun ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Thermal Decomposition ◽  
Preexponential Factor ◽  
Decomposition Kinetics ◽  
Algebraic Expression ◽  
X Ray Diffraction ◽  
X Ray ◽  
Carbonate Hydroxide ◽  
Kinetics Of ◽  
Scanning Electron

The thermal decomposition of ammonium aluminum carbonate hydroxide was studied under non-isothermal conditions in air. The decomposition kinetics were evaluated from data of TG-DTA by means of the Kissinger equation and the Coats-Redfern equation. The values of the activation energy E, the preexponential factor A and the algebraic expression of integral G(α) functions of the thermal decomposition were calculated. The ammonium aluminum carbonate hydroxide (AACH) was characterized by X-ray diffraction, differential thermal analysis and thermogravimetric and field emission scanning electron microscopy.

Crystallization Kinetics of Iron Rich Glass-Ceramic Obtained from Waste of Steel Industry

2014 ◽  
Vol 775-776 ◽  
pp. 244-249 ◽  
Author(s):  
André Luís Luza ◽  
Débora Cristina Niero Fabris ◽  
Edivelton Soratto Gislon ◽  
Morgana de Medeiros Machado ◽  
Oscar Rubem Klegues Montedo
Keyword(s):  
Crystallization Kinetics ◽  
Glass Ceramic ◽  
Absorption Spectrometry ◽  
Differential Analysis ◽  
X Ray Diffraction ◽  
Crystalline Phases ◽  
X Ray ◽  
Heat Treated ◽  
Wet Ground ◽  
Kinetics Of

The main objective of this work was to study the crystallization kinetics of glass-ceramic obtained from steel waste. Two compositions were melted at about 1350 °C. The obtained frits were dried and re-melted. Each composition was then wet ground, dried, and chemically characterized (X-ray fluorescence and atomic absorption spectrometry), structurally (X-ray diffraction), and thermally (thermal differential analysis). Then the powders were compacted and the samples were dried and heat treated in a kiln between 690 and 890 °C. After, the crystallized bodies were ground and the crystalline phases were identified by X-ray diffraction. Results showed that the main formed crystalline phases were magnetite, hematite, Fe2.95Si0.05O4, and CaAl2Fe4O10. The activation energies obtained by the Kissinger method were between 348 and 423 kJ.mol-1, whereas the Avrami parameter was obtained between 0.76 and 1.1 indicating surface crystallization.

scholarly journals Coordination polymers of Fe(III) with ligands derived from dinaphthyl-, dinaphthylthio- and dinaphthyldithiophosphinic acids

2002 ◽  
Vol 67 (8-9) ◽  
pp. 617-624 ◽  
Author(s):  
Ioan Rosca ◽  
Daniel Sutiman ◽  
Mihaela Vizitiu ◽  
Doina Sibiescu ◽  
Adrian Cailean ◽  
...  
Keyword(s):  
Experimental Data ◽  
Thermal Decomposition ◽  
Thermogravimetric Analysis ◽  
Coordination Polymers ◽  
Gel Chromatography ◽  
Ir Absorption ◽  
X Ray Diffraction ◽  
X Ray ◽  
Decomposition Reactions ◽  
Structural Formulae

The synthesis and the study of some coordination polymers derived from the interaction of the acetylacetonate of Fe(III) with dinaphthylphosphinic acid, dinaphthylthiophosphinic acid and dinaphthyldithiophosphinic acid are presented. The methods applied for the study were chemical analysis, gel chromatography, M?ssbauer and IR absorption spectroscopy, X-ray diffraction and thermogravimetric analysis from which the kinedic parameters of the thermal decomposition reactions were determined. The semiconductive properties of the synthesized compounds were also examined. Based on the obtained experimental data and on literature indications, the structural formulae of these compounds were assigned.

scholarly journals Stable and Metastable Phase Equilibria Involving the Cu6Sn5 Intermetallic

2021 ◽  
Author(s):  
A. Leineweber ◽  
M. Löffler ◽  
S. Martin
Keyword(s):  
Phase Equilibria ◽  
Electron Backscatter Diffraction ◽  
Metastable Phase ◽  
Stable Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Heat Treated ◽  
Ordered Phases ◽  
Backscatter Diffraction ◽  
Kinetics Of

Abstract Cu6Sn5 intermetallic occurs in the form of differently ordered phases η, η′ and η′′. In solder joints, this intermetallic can undergo changes in composition and the state of order without or while interacting with excess Cu and excess Sn in the system, potentially giving rise to detrimental changes in the mechanical properties of the solder. In order to study such processes in fundamental detail and to get more detailed information about the metastable and stable phase equilibria, model alloys consisting of Cu3Sn + Cu6Sn5 as well as Cu6Sn5 + Sn-rich melt were heat treated. Powder x-ray diffraction and scanning electron microscopy supplemented by electron backscatter diffraction were used to investigate the structural and microstructural changes. It was shown that Sn-poor η can increase its Sn content by Cu3Sn precipitation at grain boundaries or by uptake of Sn from the Sn-rich melt. From the kinetics of the former process at 513 K and the grain size of the η phase, we obtained an interdiffusion coefficient in η of (3 ± 1) × 10−16 m2 s−1. Comparison of this value with literature data implies that this value reflects pure volume (inter)diffusion, while Cu6Sn5 growth at low temperature is typically strongly influenced by grain-boundary diffusion. These investigations also confirm that η′′ forming below a composition-dependent transus temperature gradually enriches in Sn content, confirming that Sn-poor η′′ is metastable against decomposition into Cu3Sn and more Sn-rich η or (at lower temperatures) η′. Graphic Abstract

Study on Adsorption of Crosslinked Starch Microspheres towards Heavy Metal Ions

2013 ◽  
Vol 834-836 ◽  
pp. 531-535
Author(s):  
Li Yan Yang ◽  
Yi Hui Guo ◽  
Li Li Yu ◽  
Jing You
Keyword(s):  
Metal Ions ◽  
Reversed Phase ◽  
Adsorption Rate ◽  
X Ray Diffraction ◽  
Adsorption Selectivity ◽  
X Ray ◽  
Starch Microsphere ◽  
Other Substances ◽  
Effects Of Media ◽  
Kinetics Of

A type of cross-linking starch microsphere (CSMs) has been synthesized via reversed phase suspension method. Crosslinked starch microsphere has good adsorption performance to metal ions in water. The adsorption kinetics of Co (II) on the CSMs, selectivity of adsorption CSMs towards Co (II),Cu (II),Pb (II),Cd (II) and adsorption effects of media towards Co (II) were investigated. The CSMs and its adsorption product were comparatively characterized by X-ray diffraction (XRD). The results showed that The adsorption rate is mainly controlled by liquid film diffusion, and the constant of adsorption rate is 0.0686min-1 at 308K. The crystal structure of the CSMs decreased greatly after the incorporation of Co (II). Co (II) has better adsorption selectivity on CSMs. Ions coexist and other substances in the solution have certain impact on adsorption. Those data are helpful for treatment of the wastewater containing heavy ions.

Efficient adsorption of chlorpyrifos onto modified activated carbon by gamma irradiation; a plausible adsorption mechanism

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Mohamed S. Yahia ◽  
Ahmed S. Elzaref ◽  
Magdy B. Awad ◽  
Ahmed M. Tony ◽  
Ahmed S. Elfeky
Keyword(s):  
Gamma Irradiation ◽  
Area Measurement ◽  
Maximum Adsorption Capacity ◽  
X Ray Diffraction ◽  
X Ray ◽  
First Order ◽  
Pseudo Second Order ◽  
Ft Ir ◽  
Pseudo First Order ◽  
Kinetics Of

Abstract Commercial Granulated Active Carbon (GAC) has been modified using 10 Gy dose Gamma irradiation (GAC10 Gy) for increasing its ability of air purification. Both, the raw and treated samples were applied for removing Chlorpyrifos pesticide (CPF) from ambient midair. Physicochemical properties of the two materials were characterized by Fourier Transform Infrared (FT-IR) and Raman spectroscopy. The phase formation and microstructure were monitored using X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), supported with Energy-Dispersive X-ray (EDX). The Surface area measurement was detected using BET particle size prosometry. Obtained outcomes showed that, the maximum adsorption capacity, given by Langmuir equations, was greatly increased from 172.712 to 272.480 mg/g for GAC and GAC10 Gy, respectively, with high selectivity. The overall removal efficiency of GAC10 Gy was notably comparable to that of the original GAC-sorbent. The present study indicated that, gamma irradiation could be a promising technique for treating GAC and turned it more active in eliminating the pesticides pollutants from surrounding air. The data of equilibrium has been analyzed by Langmuir and Freundlich models, that were considerably better suited for the investigated materials than other models. The process kinetics of CPF adsorbed onto both tested carbon versions were found to obey the pseudo first order at all concentrations with an exception at 70 mg/l using GAC, where, the spontaneous exothermic adsorption of Chlorpyrifos is a strong function for the pseudo-first order (PFO) and pseudo second order (PSO) kinetics.

scholarly journals Hydrothermal Ageing and Its Effect on Fracture Load of Zirconia Dental Implants

Materials ◽  
2021 ◽  
Vol 14 (11) ◽  
pp. 3103
Author(s):  
Laurent Gremillard ◽  
Agnès Mattlet ◽  
Alexandre Mathevon ◽  
Damien Fabrègue ◽  
Bruno Zberg ◽  
...  
Keyword(s):  
Dental Implants ◽  
Fracture Load ◽  
Accelerated Ageing ◽  
Dental Ceramics ◽  
X Ray Diffraction ◽  
X Ray ◽  
Dental Restorations ◽  
Different Temperatures ◽  
Mechanical Performances ◽  
Kinetics Of

Due to growing demand for metal-free dental restorations, dental ceramics, especially dental zirconia, represent an increasing share of the dental implants market. They may offer mechanical performances of the same range as titanium ones. However, their use is still restricted by a lack of confidence in their durability and, in particular, in their ability to resist hydrothermal ageing. In the present study, the ageing kinetics of commercial zirconia dental implants are characterized by X-ray diffraction after accelerated ageing in an autoclave at different temperatures, enabling their extrapolation to body temperature. Measurements of the fracture loads show no effect of hydrothermal ageing even after ageing treatments simulated a 90-year implantation.

scholarly journals Leaching Titaniferous Magnetite Concentrate by Alkaline Aqueous Solution

2021 ◽  
Author(s):  
Ke Guo ◽  
Shaoyan Wang ◽  
Renfeng Song ◽  
Zhiqiang Zhang
Keyword(s):  
Aqueous Solution ◽  
Alkali Concentration ◽  
Water Usage ◽  
X Ray Diffraction ◽  
High Concentration ◽  
X Ray ◽  
Iron Concentrate ◽  
Titaniferous Magnetite ◽  
Magnetite Concentrate ◽  
Kinetics Of

AbstractLeaching titaniferous magnetite concentrate with alkali solution of high concentration under high temperature and high pressure was utilized to improve the grade of iron in iron concentrate and the grade of TiO2 in titanium tailings. The titaniferous magnetite concentrate in use contained 12.67% TiO2 and 54.01% Fe. The thermodynamics of the possible reactions and the kinetics of leaching process were analyzed. It was found that decomposing FeTiO3 with NaOH aqueous solution could be carried out spontaneously and the reaction rate was mainly controlled by internal diffusion. The effects of water usage, alkali concentration, reaction time, and temperature on the leaching procedure were inspected, and the products were characterized by X-ray diffraction, scanning electron microscope, and energy dispersive spectroscopy, respectively. After NaOH leaching and magnetic separation, the concentrate, with Fe purity of 65.98% and Fe recovery of 82.46%, and the tailings, with TiO2 purity of 32.09% and TiO2 recovery of 80.79%, were obtained, respectively.

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