scholarly journals The Effect of Alkali Roasting Pretreatment on Nickel Extraction from Limonite Ore by Using Dissolved SO2-Air

Minerals ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. 701
Author(s):  
Winny Wulandari ◽  
Meiyer Marthen Kinda ◽  
Rahmaditha Murida ◽  
Tjokorde Walmiki Samadhi
Keyword(s):  
Absorption Spectrometry ◽  
Combination Method ◽  
Low Grade ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Nickel Extraction ◽  
Nickel Recovery ◽  
Alkali Compounds ◽  
Decomposition Behavior ◽  
Hydrometallurgical Method

Extraction of limonite ore using dissolved SO2–air is an alternative hydrometallurgical method for nickel recovery. This process is carried out at atmospheric pressure and is shown to have good selectivity of nickel over iron, but with a low recovery yield. The literature refers to the application of alkali roasting as pretreatment in laterite ore leaching to increase nickel recovery. Thus, this study aims to apply the combination method of alkali roasting and leaching to extract nickel from limonite ore (1.33% Ni, 46.61% Fe) from the Southeast Sulawesi region. Three alkali compounds were included in the study (NaOH, Na2CO3 and Na2SO4). The batch-leaching process was carried out at pH 1 and 3 and temperatures of 55 and 80 °C for 180 min. The leach liquors were sampled at 15, 60, 90 and 120 min, and concentrations of the extracted metals were measured by Atomic Absorption Spectrometry (AAS). A mineralogy characterization of the raw ore and its residue after leaching was undertaken by using X-Ray Diffraction (XRD), while the thermal decomposition behavior of the ore was characterized by Thermogravimetry Analyzer (TGA)/Differential Scanning Calorimetry (DSC). The addition of Na2CO3, Na2SO4 and NaOH in the ore pretreatment increases nickel recovery from 14.80% without alkali roasting to 23.99%, 28.15% and 39.22%, respectively. The optimum extraction condition for nickel recovery is at pH 1 and a temperature of 80 °C. However, the highest Ni/Fe selectivity of 24,947 is obtained at pH 3 and a temperature of 80 °C, preceded by roasting in the absence of alkali. Compared to other hydrometallurgical processes, the process studied in this work exhibits lower recovery, but provides an alternative to extract nickel from low-grade limonite ore.

scholarly journals Extraction of Boron from Ludwigite Ore: Mechanism of Soda-Ash Roasting of Lizardite and Szaibelyite

Minerals ◽  
2019 ◽  
Vol 9 (9) ◽  
pp. 533 ◽  
Author(s):  
Xin Zhang ◽  
Guanghui Li ◽  
Jinxiang You ◽  
Jian Wang ◽  
Jun Luo ◽  
...  
Keyword(s):  
Sodium Carbonate ◽  
Energy Dispersive Spectrometer ◽  
Low Grade ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Selective Activation ◽  
X Ray ◽  
Shed Light ◽  
Soda Ash ◽  
Scanning Electron

Ludwigite ore is a typical low-grade boron ore accounting for 58.5% boron resource of China, which is mainly composed of magnetite, lizardite and szaibelyite. During soda-ash roasting of ludwigite ore, the presence of lizardite hinders the selective activation of boron. In this work, lizardite and szaibelyite were prepared and their soda-ash roasting behaviors were investigated using thermogravimetric-differential scanning calorimetry (TG-DSC), X-ray diffraction (XRD), and scanning electron microscope and energy dispersive spectrometer (SEM-EDS) analyses, in order to shed light on the soda-ash activation of boron within ludwigite ore. Thermodynamics of Na2CO3-MgSiO3-Mg2SiO4-Mg2B2O5 via FactSage show that the formation of Na2MgSiO4 was preferential for the reaction between Na2CO3 and MgSiO3/Mg2SiO4. While, regarding the reaction between Na2CO3 and Mg2B2O5, the formation of NaBO2 was foremost. Raising temperature was beneficial for the soda-ash roasting of lizardite and szaibelyite. At a temperature lower than the melting of sodium carbonate (851 °C), the soda-ash roasting of szaibelyite was faster than that of lizardite. Moreover, the melting of sodium carbonate accelerated the reaction between lizardite with sodium carbonate.

scholarly journals Electrochemical deposition of coatings of highly entropic alloys from non-aqueous solutions

2016 ◽  
Vol 60 (1) ◽  
pp. 6-12 ◽  
Author(s):  
V. Jeníček ◽  
L. Diblíková ◽  
M. Bláhová
Keyword(s):  
Aqueous Solutions ◽  
Electrochemical Deposition ◽  
Absorption Spectrometry ◽  
New Materials ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Electrochemical Coating ◽  
First Results ◽  
Combination Of Methods

Abstract The paper deals with electrochemical deposition of coatings of highly entropic alloys. These relatively new materials have been recently intensively studied. The paper describes the first results of electrochemical coating with highly entropic alloys by deposition from non-aqueous solutions. An electrochemical device was designed and coatings were deposited. The coatings were characterised with electronic microscopy scanning, atomic absorption spectrometry and X-ray diffraction methods and the combination of methods of thermic analysis of differential scanning calorimetry and thermogravimetry.

scholarly journals Preparation of Co Nanocrystallites by Solvothermal Process and Its Catalytic Activity on the Thermal Decomposition of Ammonium Perchlorate

2010 ◽  
Vol 2010 ◽  
pp. 1-5 ◽  
Author(s):  
Shusen Zhao ◽  
Dongxu Ma
Keyword(s):  
Thermal Decomposition ◽  
Catalytic Activity ◽  
Ammonium Perchlorate ◽  
Catalytic Performance ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Polyol Medium ◽  
Decomposition Behavior

Nanometer cobalt ferrite (Co) was synthesized by polyol-medium solvothermal method and characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), and selected area electron diffraction (SAED). Further, the catalytic activity and kinetic parameters of Co nanocrystallites on the thermal decomposition behavior of ammonium perchlorate (AP) have been investigated by thermogravimetry and differential scanning calorimetry analysis (TG-DSC). The results imply that the catalytic performance of Co nanocrystallites is significant and the decrease in the activation energy and the increase in the rate constant for AP further confirm the enhancement in catalytic activity of Co nanocrystallites. A mechanism based on an proton transfer process has also been proposed for AP in the presence of Co nanocrystallites.

Synthesis and Characterization of Nanocrystalline Barium–Samarium Titanate

2016 ◽  
Vol 35 (5) ◽  
pp. 499-505 ◽  
Author(s):  
M. M. Hessien ◽  
Nader El-Bagoury ◽  
M. H. H. Mahmoud ◽  
Osama M. Hemeda
Keyword(s):  
Annealing Temperature ◽  
Crystalline Size ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Analysis Measurement ◽  
Lower Annealing Temperature ◽  
Precursor Route ◽  
Decomposition Behavior ◽  
Dominant Structure

AbstractBarium–samarium titanate nanopowder (Ba0.85 Sm0.1TiO3) was synthesized through tartrate precursor route. The effect of annealing temperature on the formation, crystalline size, morphology and magnetic properties was systematically studied. The annealing temperature was varied from 600°C to 1,100°C. Thermal analysis measurement (TG-DSC, thermogravimetry-differential scanning calorimetry) was carried out on the precursor to characterize the thermal decomposition behavior. The results showed that the precursor of Ba–Sm–Ti mixture decomposed thermally in multistep weight loss up to about 480°C and perovskite Ba0.85Sm0.1TiO3 started to form at ~520°C. X-ray diffraction and Fourier transform infrared (FTIR) spectroscopic measurements showed that the synthesized Ba0.85Sm0.1TiO3 has a tetragonal dominant structure with the presence of intermediate SmTi2O3 at lower annealing temperature. The ratio of SmTi2O3 was decreased and completely disappeared at higher annealing temperatures. The tetragonality, the theoretical density and the crystalline size were increased by increasing annealing temperature. The crystalline size is still in nano-range of 12.4–19.9 nm even after annealing at 1,100°C. The morphology of the produced sample transferred from nano-cubes to nano-whisker to nano-mace (nano-aggregates) with the increase of annealing temperature.

Utilization of Metabolic Citric Acid from Aspergillus niger Using Corn Starch in the Nickel Leaching of Indonesian Saprolitic Ore

2015 ◽  
Vol 1130 ◽  
pp. 251-254
Author(s):  
Widi Astuti ◽  
Tsuyoshi Hirajima ◽  
Keiko Sasaki ◽  
Naoko Okibe
Keyword(s):  
Citric Acid ◽  
Carbon Source ◽  
Acid Concentration ◽  
Atmospheric Pressure ◽  
Corn Starch ◽  
Low Grade ◽  
Citric Acid Concentration ◽  
Nickel Extraction ◽  
Nickel Recovery ◽  
Nickel Leaching

Citric acid has been proved to be the most effective organic acid for nickel extraction from nickel lateritic ores. Citric acid can be produced from fungal metabolism by utilizing several types of carbon source as fungal nutrient. In the current experiment, production of metabolic citric acid from metabolism of Aspergillus niger by using corn starch as a carbon source was investigated. The application of the citric acid produced in the leaching of nickel from Indonesian saprolitic ore under atmospheric pressure was also conducted. The optimum citric acid concentration (i.e. around 0.05 M) can be produced by using 5% w/v of corn starch after 5 days incubation of A. niger, 30°C of temperature, shaker speed of 120 rpm, and 3% v/v of methanol as an additive. The metal leaching of Indonesian saprolitic ore was conducted using <75μm of ore particle size, 5% w/v of pulp density and 200 rpm of shaker speed at different leaching temperatures (30°C, 40°C, and 60°C). The results showed that the optimum nickel recovery (around 40%) can be reached after 3 days of leaching process at 40°C. It was also found that the use of metabolic citric acid was more effective for nickel leaching compared to the use of chemical citric acid at similar citric acid concentration (i.e. 0.05 M). It can be concluded that the metabolic citric acid produced from corn starch by A. niger will be an excellent leaching reagent for extracting nickel from low-grade Indonesian saprolitic ore.

scholarly journals Propolis and Organosilanes as Innovative Hybrid Modifiers in Wood-Based Polymer Composites

Materials ◽  
2021 ◽  
Vol 14 (2) ◽  
pp. 464
Author(s):  
Majka Odalanowska ◽  
Magdalena Woźniak ◽  
Izabela Ratajczak ◽  
Daria Zielińska ◽  
Grzegorz Cofta ◽  
...  
Keyword(s):  
Trichoderma Viride ◽  
Antimicrobial Properties ◽  
Absorption Spectrometry ◽  
Strength Properties ◽  
Tetraethyl Orthosilicate ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Propolis Extract ◽  
Polypropylene Matrix

The article presents characteristics of wood/polypropylene composites, where the wood was treated with propolis extract (EEP) and innovative propolis-silane formulations. Special interest in propolis for wood impregnation is due to its antimicrobial properties. One propolis-silane formulation (EEP-TEOS/VTMOS) consisted of EEP, tetraethyl orthosilicate (TEOS), and vinyltrimethoxysilane (VTMOS), while the other (EEP-TEOS/OTEOS) contained EEP, tetraethyl orthosilicate (TEOS), and octyltriethoxysilane (OTEOS). The treated wood fillers were characterized by Fourier transform infrared spectroscopy (FTIR), atomic absorption spectrometry (AAS), and X-ray diffraction (XRD), while the composites were investigated using differential scanning calorimetry (DSC), X-ray diffraction (XRD), and optical microscopy. The wood treated with EEP and propolis-silane formulations showed resistance against moulds, including Aspergillus niger, Chaetomium globosum, and Trichoderma viride. The chemical analyses confirmed presence of silanes and constituents of propolis in wood structure. In addition, treatment of wood with the propolis-silane formulations produced significant changes in nucleating abilities of wood in the polypropylene matrix, which was confirmed by an increase in crystallization temperature and crystal conversion, as well as a decrease in half-time of crystallization parameters compared to the untreated polymer matrix. In all the composites, the formation of a transcrystalline layer was observed, with the greatest rate recorded for the composite with the filler treated with EEP-TEOS/OTEOS. Moreover, impregnation of wood with propolis-silane formulations resulted in a considerable improvement of strength properties in the produced composites. A dependence was found between changes in the polymorphic structures of the polypropylene matrix and strength properties of composite materials. It needs to be stressed that to date literature sources have not reported on treatment of wood fillers using bifunctional modifiers providing a simultaneous effect of compatibility in the polymer-filler system or any protective effect against fungi.

scholarly journals Column Leaching of Greek Low-Grade Limonitic Laterites

Minerals ◽  
2018 ◽  
Vol 8 (9) ◽  
pp. 377 ◽  
Author(s):  
Kostas Komnitsas ◽  
Evangelos Petrakis ◽  
Olga Pantelaki ◽  
Anna Kritikaki
Keyword(s):  
Leach Solution ◽  
Low Grade ◽  
Test Duration ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Column Leaching ◽  
X Ray ◽  
H2so4 Concentration ◽  
Peristaltic Pumps ◽  
Leaching Solution

In this study, column leaching experiments were carried out to investigate the extraction of Ni and Co from low-grade limonitic laterites from Agios Ioannis mines in central Greece. Tests were carried out in laboratory Plexiglas columns using H2SO4 as leaching solution. Parameters determining the efficiency of the process, i.e., acid concentration (0.5 M or 1.5 M) and addition of 20 or 30 g/L of sodium sulfite (Na2SO3) in the leaching solution, were also studied. Upflow transport of the leaching solution with the use of peristaltic pumps was carried out, while the pregnant leach solution (PLS) was recycled several times over the entire test duration. The concentration of Ni, Co, Fe, Ca, Al, Mg, and Mn in the PLS was determined by Atomic Absorption Spectroscopy (AAS). The ore and the leaching residues were characterized by different techniques, i.e., X-ray fluorescence (XRF), X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, and differential scanning calorimetry and thermogravimetry (DSC/TG). The experimental results showed that (i) Ni and Co extractions increased with the increase of H2SO4 concentration—60.2% Ni and 59.0% Co extractions were obtained after 33 days of leaching with 1.5 M H2SO4; (ii) addition of 20 g/L Na2SO3 in the leaching solution resulted in higher extraction percentages for both metals (73.5% for Ni and 84.1% for Co, respectively), whereas further increase of Na2SO3 concentration to 30 g/L only marginally affected Ni and Co extractions; and (iii) when leaching was carried out with 1.5 M H2SO4 and 20 g/L Na2SO3, its selectivity was improved, as deduced from the ratios Ni/Mg, Ni/Ca and Ni/Al in the PLS; on the other hand, the ratio Ni/Fe dropped as a result of the higher Fe extraction compared with that of Ni.

Synthesis, crystal structure, and properties of energetic copper(II) compound based on 3,5-dinitrobenzoic acid and imidazole

2021 ◽  
Vol 19 (4) ◽  
pp. 295-304
Author(s):  
Bi-Dong Wu ◽  
Da-Wei Ren ◽  
Zhi-min Li ◽  
Jing-Yu Wang ◽  
Chong-wei An ◽  
...  
Keyword(s):  
Isothermal Kinetics ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Kinetics Parameters ◽  
Ftir Characterization ◽  
Kissinger’S Method ◽  
Potential Applications ◽  
Solid Rocket ◽  
Decomposition Behavior ◽  
Friction Sensitivity

Energetic copper(II) compound was synthesized based on 3,5-dinitrobenzoic acid (HDNBA) and imidazole (IMI), and characterized by elemental analysis and FTIR characterization. Single-crystal X-ray diffraction analysis revealed that [Cu(IMI)2(DNBA)2] (1) belongs to monoclinic, pertains to P21/c space group, β= 96.195(2) and Dc= 1.742 g cm–3. Cu(II) ion was coordinated to a plane tetragon, by two oxygen atoms and two nitrogen atoms from different DNBA ions and IMI ligands, which of them present typical monodentate coordination mode. Differential scanning calorimetry (DSC) was applied to assess the thermal decomposition behavior of 1. The non-isothermal kinetics parameters were calculated by the Kissinger’s method, Ozawa’s method and Starink’s method, respectively. Impact sensitivity and friction Sensitivity were also determined by standard method. In the end, the catalytic effects on the decomposition of ammonium perchlorate (AP), HMX and RDX of 1 were studied by DSC. All results supported the potential applications of the energetic complex 1 as additive of solid rocket propellant.

Glibenclamide-Nicotinamide Cocrystals Synthesized by The Solvent Evaporation Method to Enhance Solubility and Dissolution Rate of Glibenclamide

2019 ◽  
Vol 9 (01) ◽  
pp. 21-26
Author(s):  
Arif Budiman ◽  
Ayu Apriliani ◽  
Tazyinul Qoriah ◽  
Sandra Megantara
Keyword(s):  
Solvent Evaporation ◽  
Physical Mixture ◽  
Dissolution Profile ◽  
Solvent Evaporation Method ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Evaporation Method ◽  
Dissolution Properties ◽  
Mixture Characterization

Purpose: To develop glibenclamide-nicotinamide cocrystals with the solvent evaporation method and evaluate their solubility and dissolution properties. Methods: Cocrystals of glibenclamide-nicotinamide (1:2) were prepared with the solvent evaporation method. The prediction of interactive cocrystals was observed using in silico method. The solubility and dissolution were performed as evaluation of cocrystals. The cocrystals also were characterized by differential scanning calorimetry (DSC), infrared spectrophotometry, and powder X-ray diffraction (PXRD). Result: The solubility and dissolution profile of glibenclamide-nicotinamide cocrystal (1:2) increased significantly compared to pure glibenclamide as well as its physical mixture. Characterization of cocrystal glibenclamide-nicotinamide (1:2) including infrared Fourier transform, DSC, and PXRD, indicated the formation of a new solid crystal phase differing from glibenclamide and nicotinamide. Conclusion: The confirmation of cocrystal glibenclamide-nicotinamide (1:2) indicated the formation of new solid crystalline phases that differ from pure glibenclamide and its physical mixture

Studies on the Preparation, Characterization and Solubility of -Cyclodextrin-Roxythromycin Inclusion Complexes

2009 ◽  
Vol 2 (2) ◽  
pp. 523-530
Author(s):  
D. Nagasamy Venkatesh ◽  
S. Karthick ◽  
M. Umesh ◽  
G. Vivek ◽  
R.M. Valliappan ◽  
...  
Keyword(s):  
Dissolution Rate ◽  
Inclusion Complexes ◽  
Phase Solubility ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Ir Studies ◽  
Poorly Soluble ◽  
Poorly Soluble Drug

Roxythromycin/ β-cyclodextrin (Roxy/ β-CD) dispersions were prepared with a view to study the influence of β-CD on the solubility and dissolution rate of this poorly soluble drug. Phase-solubility profile indicated that the solubility of roxythromycin was significantly increased in the presence of β-cyclodextrin and was classified as AL-type, indicating the 1:1 stoichiometric inclusion complexes. Physical characterization of the prepared systems was carried out by differential scanning calorimetry (DSC), X-ray diffraction studies (XRD) and IR studies. Solid state characterization of the drug β-CD binary system using XRD, FTIR and DSC revealed distinct loss of drug crystallinity in the formulation, ostensibly accounting for enhancement of dissolution rate.

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