scholarly journals Effective Removal of Barrier Layer on the Surface of Low-Nickel Matte in an FeCl3-HCl-H2O Solution

Minerals ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 1219
Author(s):  
Chuncheng Zhu ◽  
Yu Lei ◽  
Xinbo Hu ◽  
Qian Xu ◽  
Xingli Zou ◽  
...  
Keyword(s):  
Particle Size ◽  
Quartz Sand ◽  
Inductively Coupled Plasma ◽  
Control Variable ◽  
Mechanical Agitation ◽  
Experimental Conditions ◽  
X Ray ◽  
Main Metal ◽  
Nickel Matte ◽  
Leaching Reaction

Using ferric chloride as an oxidant, here, we investigated the leaching effect of low-nickel matte in a flow field produced by mechanical agitation. The factors affecting a leaching reaction, such as stirring speed, leaching time, low-nickel matte particle size, and inert abrasive quartz sand, were studied. X-ray diffraction (XRD), X-ray fluorescence spectroscopy (XRF), a laser particle size analyzer, optical microscopy (OM), a scanning electron microscopy (SEM) with an energy dispersive X-ray detector (EDS), and a Raman spectrometer were used to characterize the materials before and after the leaching reaction. The contents of the main metal ions such as Ni, Cu, and Co in the leaching solution were analyzed by inductively coupled plasma atomic emission spectroscopy (ICP-AES). Using the control variable method, the optimal experimental conditions were as follows: 2 mol/L FeCl3—0.5 mol/L HCl-H2O system with low-nickel matte and quartz sand (mass ratio is 1:5) and leaching at 90 °C for 8 h. The results showed that the blocking effect of the solid product sulfur layer was effectively removed and continuous leaching was realized. The leaching efficiencies of Ni, Cu, and Co were 98.9%, 99.3%, and 98.1%, respectively.

Processing of granite quarry solid waste into industrial high silica materials using leaching process with HCl concentration variation

2020 ◽  
Vol 11 (2) ◽  
pp. 43-50
Author(s):  
Yusup Hendronursito ◽  
Muhammad Amin ◽  
Slamet Sumardi ◽  
Roniyus Marjunus ◽  
Frista Clarasati ◽  
...  
Keyword(s):  
Particle Size ◽  
Rotational Speed ◽  
Inductively Coupled Plasma ◽  
Chemical Elements ◽  
Silica Content ◽  
X Ray ◽  
Concentration Variation ◽  
Leaching Process ◽  
Hcl Concentration ◽  
Granite Powder

This study was aimed to increase granite's silica content using the leaching process with HCl concentration variation. The granite used in this study came from Lematang, South Lampung. This study aims to determine the effect of variations in HCl concentration, particle size, and rotational speed on the crystalline phase and chemical elements formed in the silica product produced from granite. The HCl concentration variations were 6.0 M, 7.2 M, 8.4 M, and 9.6 M, the variation in particle size used was 270 and 400 mesh. Variations in rotational speed during leaching were 500 and 750 rpm. Granite powder was calcined at 1000 ºC for 2 hours. Characterization was performed using X-Ray Fluorescence (XRF), X-Ray Diffraction (XRD), and Inductively Coupled Plasma-Optical Emission Spectroscopy (ICP- OES). The results showed that the silica content increased with increasing HCl concentration, the finer the particle size, and the higher the rotational speed. XRF analysis showed that the silica with the highest purity was leached with 9.6 HCl with a particle size of 400 mesh and a rotational speed of of 750 rpm, which was 73.49%. Based on the results above, by leaching using HCl, the Si content can increase from before. The XRD diffractogram showed that the granite powder formed the Quartz phase.

scholarly journals Compression of Aggregates of Acid-Leached Coal Gangues: Implications for Coal Mine Backfill

2018 ◽  
Vol 2018 ◽  
pp. 1-13
Author(s):  
Wenyue Qi ◽  
Jixiong Zhang ◽  
Qiang Zhang
Keyword(s):  
Mechanical Properties ◽  
Particle Size ◽  
Inductively Coupled Plasma ◽  
Acid Leaching ◽  
Optical Emission ◽  
Chemical Compositions ◽  
X Ray ◽  
Inductively Coupled ◽  
Effects Of Ph ◽  
Compaction Stress

The compression mechanical properties of coal gangues subjected to acidic immersion were examined using a cylinder and a YAS-500 electrohydraulic servotesting system in order to investigate the effects of pH and particle size on its compaction stress-strain and stress-compaction relationships. The evolutionary trends of the leaching solution’s pH at various immersion times during the coal gangue corrosion process were analyzed. Then, inductively coupled plasma optical emission spectroscopy (ICP-OES) was performed on the leaching solutions to determine their chemical compositions and concentrations. An X-ray diffractometer (XRD) and X-ray fluorescence (XRF) spectroscopy also performed qualitative and quantitative analyses of the coal gangues samples. The mechanisms of hydrochemical corrosion in coal gangues were ultimately elucidated by analyzing these results, taking into consideration the chemical reactions of the acidic solutions and coal gangues. The results indicate that hydrochemical damage in coal gangues is more sensitive to small particle size and stronger acidity. The compressive mechanical properties of coal gangues that had been immersed demonstrated that their bearing capacity decreased as the particle sizes decreased and acidity increased. It was also established that acid leaching changes the mineral composition, particles, and pores of coal gangues, thus degrading their compressive mechanical properties.

scholarly journals Cr6+ adsorption by modified vermiculite

2020 ◽  
Author(s):  
Valeria Medoro ◽  
Celia Marcos Pascual ◽  
Giacomo Ferretti ◽  
Giulio Galamini ◽  
Massimo Coltorti
Keyword(s):  
Earth Sciences ◽  
Inductively Coupled Plasma ◽  
Contact Time ◽  
Second Order ◽  
Isotherm Models ◽  
Maximum Adsorption Capacity ◽  
Order Kinetic ◽  
Experimental Conditions ◽  
X Ray ◽  
Pseudo Second Order

<p><strong>Abstract</strong>: <strong>Cr<sup>6+</sup> adsorption by modified vermiculite</strong></p><p><strong> </strong></p><p>Valeria Medoro- University of Ferrara , Department of Physics and Earth Sciences, Italy</p><p>Celia Marcos Pascual-University of Oviedo, Department of Geology, Spain</p><p>Giacomo Ferretti- University of Ferrara , Department of Physics and Earth Sciences, Italy</p><p>Giulio Galamini- University of Ferrara , Department of Physics and Earth Sciences, Italy</p><p>Massimo Coltorti- University of Ferrara , Department of Physics and Earth Sciences, Italy</p><p> </p><p>This work aimed at investigating the adsorption of Cr<sup>6+</sup> in water by exfoliated vermiculite. The adsorbant tested in this experiment was a vermiculite (from China) which has been subjected to heating at 1000 °C for 1 minute, resulting in an exfoliated vermiculite.</p><p>Three effects were studied: 1) contact time; 2) initial concentracion of Cr<sup>6+</sup>; 3) adsorbent mass. Samples were analysed by X Ray Fluorescence (XRF), X Ray Diffraction (XRD) and the solutions with Inductively Coupled Plasma Mass Spectrometry (ICP-MS) to quantify the adsorbed Cr<sup>6+</sup> by the vermiculite.</p><p>Results from XRD diffraction showed a conversion of vermiculite into flogopite  after heating at 1000°C for 1 minute because of: 1) high content of potassium, 2) dehydration and 3) structural re-ordering; after the contact of vermiculite with Cr<sup>6+</sup>, the mineral structure did not change. The adsorption of Cr<sup>6+</sup> was studied by Langmuir, Freundlich and Dubinin-Kaganer-Radushkevich (DKR) isotherm models. DKR model, indicative of a cooperative process, described adsorption equilibrium better than the other two models and the maximum adsorption capacity obtained was of 2.81 mol/g. Kinetic was studied using pseudo-first and pseudo-second order kinetic models, with a better description of the process by pseudo-second order model with correlation coefficient almost unitary (R<sup>2</sup>=0.9984; other kinetic parameters were k<sub>2</sub>=0.0015 and the absorption initial rate of 0.2x10<sup>-8</sup> mg g<sup>-1</sup> h<sup>-1</sup>). </p><p>The present study demonstrates the effectiveness of modified vermiculite adsorbents for the treatment of hexavalent chromium-contaminated waters and that its adsorption depends on the experimental conditions (such as contact time, initial concentracion of Cr<sup>6+</sup> and adsorbent mass).</p>

Optimizing conditions for x-ray microchemical analysis in analytical electron microscopy

1978 ◽  
Vol 36 (1) ◽  
pp. 548-549 ◽  
Author(s):  
N. J. Zaluzec
Keyword(s):  
Solid Angle ◽  
Analytical Electron Microscopy ◽  
Incident Beam ◽  
Thin Foil ◽  
Experimental Conditions ◽  
X Ray ◽  
Microchemical Analysis ◽  
Analytical Electron ◽  
Image Position ◽  
Incident Beam Energy

The ultimate sensitivity of microchemical analysis using x-ray emission rests in selecting those experimental conditions which will maximize the measured peak-to-background (P/B) ratio. This paper presents the results of calculations aimed at determining the influence of incident beam energy, detector/specimen geometry and specimen composition on the P/B ratio for ideally thin samples (i.e., the effects of scattering and absorption are considered negligible). As such it is assumed that the complications resulting from system peaks, bremsstrahlung fluorescence, electron tails and specimen contamination have been eliminated and that one needs only to consider the physics of the generation/emission process.The number of characteristic x-ray photons (Ip) emitted from a thin foil of thickness dt into the solid angle dΩ is given by the well-known equation

The effect of Tin additionon on Structural and magnetic properties of the stannoferrite Li0.5+0.5XFe2.5-1.5XSnXO4

2016 ◽  
Vol 12 (3) ◽  
pp. 4307-4321 ◽  
Author(s):  
Ahmed Hassan Ibrahim ◽  
Yehia Abbas
Keyword(s):  
Particle Size ◽  
Fine Particles ◽  
Magnetic Moments ◽  
Lithium Ferrite ◽  
Tem Analysis ◽  
Weiss Temperature ◽  
X Ray ◽  
Two Phases ◽  
Nanocrystalline Ferrite ◽  
20 Nm

The physical properties of ferrites are verysensitive to microstructure, which in turn critically dependson the manufacturing process.Nanocrystalline Lithium Stannoferrite system Li0.5+0.5XFe2.5-1.5XSnXO4,X= (0, 0.2, 0.4, 0.6, 0.8 and 1.0) fine particles were successfully prepared by double sintering ceramic technique at pre-sintering temperature of 500oC for 3 h andthepre-sintered material was crushed and sintered finally in air at 1000oC.The structural and microstructural evolutions of the nanophase have been studied using X-ray powder diffraction (XRD) and the Rietveld method.The refinement results showed that the nanocrystalline ferrite has a two phases of ordered and disordered phases for polymorphous lithium Stannoferrite.The particle size of as obtained samples were found to be ~20 nm through TEM that increases up to ~ 85 nmand isdependent on the annealing temperature. TEM micrograph reveals that the grains of sample are spherical in shape. (TEM) analysis confirmed the X-ray results.The particle size of stannic substituted lithium ferrite fine particle obtained from the XRD using Scherrer equation.Magneticmeasurements obtained from lake shore’s vibrating sample magnetometer (VSM), saturation magnetization ofordered LiFe5O8 was found to be (57.829 emu/g) which was lower than disordered LiFe5O8(62.848 emu/g).Theinterplay between superexchange interactions of Fe3+ ions at A and B sublattices gives rise to ferrimagnetic ordering of magnetic moments,with a high Curie-Weiss temperature (TCW ~ 900 K).

Sorption of Se (IV) from aqueous solutions with subsequent determination by X-ray fluorescence analysis

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 ◽  
...  
Keyword(s):  
Inductively Coupled Plasma ◽  
Fluorescence Analysis ◽  
Standard Samples ◽  
Phase Contact Time ◽  
Sorbent Phase ◽  
X Ray ◽  
Fundamental Parameters ◽  
Inductively Coupled ◽  
Subsequent Determination

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.

Ultrafiltration of silica sols

1989 ◽  
Vol 54 (1) ◽  
pp. 91-101 ◽  
Author(s):  
Milan Stakić ◽  
Slobodan Milonjić ◽  
Vladeta Pavasović ◽  
Zoja Ilić
Keyword(s):  
Particle Size ◽  
Silica Particle ◽  
Specific Resistance ◽  
Membrane Surface ◽  
Membrane Resistance ◽  
Experimental Conditions ◽  
Surface Unit ◽  
Silica Sols ◽  
Filtration Flux ◽  
Batch Cell

Ultrafiltration of three laboratory made silica and two commercial silica sols was studied using Amicon YC membrane in a 200 ml capacity batch-cell. The effect of silica particle size, stirring conditions, pressure, pH and silica contents on ultrafiltration was investigated. The results obtained indicate that the smaller particles have, disregarding the stirring conditions, lower filtration flux. The differences observed in filtration flux are more pronounced in the conditions without stirring. The obtained value of the membrane resistance is independent of the conditions investigated (stirring, pressure, pH, silica contents and particle size). The values of the resistance of polarized solids, specific resistance, and the mass of gel per membrane surface unit were calculated for all experimental conditions.

scholarly journals Modification of Wood with Monoethanolamino-borate by The Data of X-Ray Photoelectron Spectroscopy

2018 ◽  
Vol 196 ◽  
pp. 04005
Author(s):  
Irina Stepina ◽  
Irina Kotlyarova
Keyword(s):  
Particle Size ◽  
Photoelectron Spectroscopy ◽  
Model Compound ◽  
Hydrolytic Stability ◽  
Photoelectron Spectra ◽  
Wood Cellulose ◽  
Rapid Loss ◽  
X Ray ◽  
Wood Protection ◽  
Cellulose Materials

The difficulty of wood protection from biocorrosion and fire is due to the fact that modifiers in use are washed out from the surface of the substrate under the influence of environmental factors. This results in a rapid loss of the protective effect and other practically important wood characteristics caused by the modification. To solve this problem is the aim of our work. Here, monoethanolaminoborate is used as a modifier, where electron-donating nitrogen atom provides a coordination number equal to four to a boron atom, which determines the hydrolytic stability of the compounds formed. Alpha-cellulose ground mechanically to a particle size of 1 mm at most was used as a model compound for the modification. X-ray photoelectron spectra were recorded on the XSAM-800 spectrometer (Kratos, UK). Prolonged extraction of the modified samples preceded the registration of the photoelectron spectra to exclude the fixation of the modifier molecules unreacted with cellulose. As a result of the experiment, boron and nitrogen atoms were found in the modified substrate, which indicated the hydrolytic stability of the bonds formed between the modifier molecules and the substrate. Therefore monoethanolaminoborate can be considered as a non-extractable modifier for wood-cellulose materials.

X-ray studies of particle size in silica

1929 ◽  
Vol 208 (1) ◽  
pp. 59-71
Author(s):  
R.H. Aborn ◽  
R.L. Davidson
Keyword(s):  
Particle Size ◽  
X Ray
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