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хлористоводородная кислота

Geotechnical Engineering and Engineering Geology
  • Date submitted
    2024-06-04
  • Date accepted
    2025-01-28
  • Date published
    2025-04-04

Impact of dry and wet magnetic separator process parameters on iron oxide removal from Egyptian feldspar ore

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The demand for feldspar as a raw material in the ceramic industry is continuously increasing. Feldspar is abundant in the Earth's crust and typically found alongside other silicate minerals, as well as titanium and iron oxides. This study aims to reduce the iron oxide content in feldspar ore from the Wadi Zirib region and achieve an optimal grade of feldspar concentrate for various industrial uses. The research involved dry and wet magnetic separation techniques followed by leaching with oxalic and citric acids to minimize iron impurities and enhance optical properties. The factors affecting the dry magnetic separation, for feldspar size of –250+45 µm, were optimized using the Box – Behnken factorial design and a non-magnetic concentrate with 0.29 % Fe2O3 and an 92.19 % feldspar yield was obtained. The wet magnetic separation for feldspar fines of size –45 µm was optimized and a concentrate with 0.27 % Fe2O3 was achieved. The acid leaching was conducted on the non-magnetic feldspar concentrates using oxalic and citric acid. Oxalic acid was more successful in reducing iron oxide of dry (to 0.19 %) and wet (to 0.12 %) non-magnetic feldspar concentrates. The optical properties of the leached concentrates were improved compared to the original sample, as the whiteness improved up to 90 %.

How to cite: Yassin K.E., El-Sayed H.R., Elbendari A.M. Impact of dry and wet magnetic separator process parameters on iron oxide removal from Egyptian feldspar ore // Journal of Mining Institute. 2025. p. EDN RWLRDI
Geotechnical Engineering and Engineering Geology
  • Date submitted
    2024-04-10
  • Date accepted
    2024-06-03
  • Date published
    2025-04-25

Combined method for processing spent acid etching solution obtained during manufacturing of titanium products

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Possessing high strength, low density and significant chemical resistance, titanium has found wide application in various fields of the national economy – the chemical industry, aviation and rocket technology, mechanical engineering, medicine, etc. The production of titanium products is hampered by a fairly strong oxide film covering its surface. Removal of the oxide film from the surface of titanium workpieces is carried out by etching in solutions of mineral acids of various compositions. A spent acid etching solution (SAES) is formed, containing titanium salt and the remainder of unreacted acids. Almost all etching solutions contain HF and one of the strong acids. This is H2SO4, HCl or HNO3. Thus, the SAES includes ions of titanium, fluorine or chlorine, orsulfate, or nitrate. SAES is quite toxic and must be diluted or cleaned several times before being discharged into a reservoir. Most of the methods used to extract impurities contained in SAES lead to a decrease in their content. As a result of such purification, there is a loss of substances contained in SAES in significant quantities and of interest for further use. The work presents experimental results obtained from the combined processing of SAES containing titanium fluoride, hydrofluoric and hydrochloric acids. At the first stage, SAES is treated with sodium hydroxide. The resulting titanium hydroxide precipitate is filtered off. At the second stage, the filtrate containing sodium fluoride and chloride is processed in a membrane electrolyzer. In this case, not only the extraction of sodium salts from the filtrate occurs, but also the production of sodium hydroxide and a mixture of hydrofluoric and hydrochloric acids. Sodium hydroxide can be used for processing SAES, and a mixture of acids for etching titanium workpieces.

How to cite: Bykovskii N.A., Kantor E.A., Shulaev N.S., Fanakov V.S. Combined method for processing spent acid etching solution obtained during manufacturing of titanium products // Journal of Mining Institute. 2025. Vol. 272 . p. 51-58. EDN OVECLL
Geotechnical Engineering and Engineering Geology
  • Date submitted
    2024-05-02
  • Date accepted
    2024-06-03
  • Date published
    2024-07-04

Iron ore tailings as a raw material for Fe-Al coagulant production

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The paper presents the results of experimental research into the recovery of Fe-Al coagulant from iron ore tailings (IOTs). The variables investigated in the laboratory tests included sulphuric acid concentration, temperature, leaching time, solid/liquid phase ratio (S:L) and the presence of stirring. The experiment determined the composition of the coagulant and the solid residue after leaching. The maximum iron content in the solution after leaching was obtained using 40 % H2SO4 at a temperature of 100 °C (or with stirring at 75 °C) and a contact time of 60 minutes. In this case, the iron yield was at the level of 25 % of the total content in the iron ore tailings. Chemical analysis of the solution obtained after leaching showed Fe and Al sulphate contents of 11 and 2 % respectively. In the next step, the efficiency of the coagulant was evaluated on model solutions of colour. The experimental results showed that the coagulant obtained from the iron ore tailings can be used for wastewater treatment in a wide pH range from 4 to 12 pH units. The solid residue after leaching is a fine-grained powder rich in silica, which can potentially be used as an artificial raw material in the construction industry. The research carried out in this thesis has shown that the extraction of coagulants from iron ore tailings can be considered as a way to extend the production chain of iron ore mining and to minimise the amount of tailings to be stored in tailing ponds. The technical solution presented in this work allows to comprehensively solve the problem of environmental protection by creating new target products for wastewater treatment from IOTs.

How to cite: Matveeva V.A., Chukaeva M.A., Semenova A.I. Iron ore tailings as a raw material for Fe-Al coagulant production // Journal of Mining Institute. 2024. Vol. 267 . p. 433-443. EDN ASOYNX
Geotechnical Engineering and Engineering Geology
  • Date submitted
    2022-10-23
  • Date accepted
    2023-02-13
  • Date published
    2023-12-25

Sorption purification of acid storage facility water from iron and titanium on organic polymeric materials

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Obtaining and production of metals from natural raw materials causes a large amount of liquid, solid, and gaseous wastes of various hazard classes that have a negative impact on the environment. In the production of titanium dioxide from ilmenite concentrate, hydrolytic sulphuric acid is formed, which includes various metal cations, their main part is iron (III) and titanium (IV) cations. Hydrolytic acid waste is sent to acid storage facilities, which have a high environmental load. The article describes the technology of ion exchange wastewater treatment of acid storage facility from iron (III) and titanium (IV) cations, which form compounds with sulphate ions and components of organic waste in acidic environments. These compounds are subjected to dispersion and dust loss during the evaporation of a water technogenic facility, especially in summer season. Sorption of complex iron (III) cations [FeSO4]+ and titanyl cations TiO2+ from sulphuric acid solutions on cation exchange resins KU-2-8, Puromet MTS9580, and Puromet MTS9560 was studied. Sorption isotherms were obtained both for individual [FeSO4]+ and TiO2+ cations and in the joint presence. The values of the equilibrium constants at a temperature of 298 K and the changes in the Gibbs energy are estimated. The capacitive characteristics of the sorbent were determined for individual cations and in the joint presence.

How to cite: Cheremisina O.V., Ponomareva M.A., Molotilova A.Y., Mashukova Y.A., Soloviev M.A. Sorption purification of acid storage facility water from iron and titanium on organic polymeric materials // Journal of Mining Institute. 2023. Vol. 264 . p. 971-980. DOI: 10.31897/PMI.2023.28
Metallurgy and concentration
  • Date submitted
    2015-12-19
  • Date accepted
    2016-02-08
  • Date published
    2016-12-23

A technique for selective extraction of ions of gold and silver from hydrochloric solutions with tributylphosphate

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Extraction is studied by tributylphosphate (TBP) of ions of gold and silver from hydrochloric solutions during the portional and single time feed of extractant in dependence of the initial concentration of metal ions, temperature, concentration of hydrochloric acid, the ratio of organic (О) and water W phases О:W. The initial solutions contained soluble complex chlorides of gold and silver. When dissolving metal chlorides in the solution of common salt and hydrochloric acid, water soluble coordinate compound are formed that contain complex anions [AuCl 2 ] – , [AuCl 4 ] – , [AgCl 2 ] – , [AgCl 3 ] 2– , [AgCl 4 ] 3– , et al. As an extractant we used the tri-butyl ether of phosphoric acid (С 4 Н 9 О) 3 РО hat belongs to oxygen containing neutral extractants. The formation of coordinate (complex) compounds of TBP and metal polychlorides may be treated as the process of solvation of the extracted metal salt by the extractant. For selective extraction of ions of gold and silver from their hydrochloric solutions by tributylphosphate it is run feeding the extractant portionally to the solution at the minimal time of contact between the solution and the extractant; it helps extracting gold almost completely with the few first portions of the extractant at concentrations of 2n HCl 240 g/dm 3 NaCl and the temperature t = 60°С. Meanwhile the extraction of silver is kept to a minimum. Silver is extracted almost completely after the extraction of gold is over; it is done with tributylphosphate as well at concentrations of 3n HCl, 240 g/dm 3 NaCl and the temperature t = 20°С.

How to cite: Voropanova L.A., Kokoeva N.B. A technique for selective extraction of ions of gold and silver from hydrochloric solutions with tributylphosphate // Journal of Mining Institute. 2016. Vol. 222 . p. 823-827. DOI: 10.18454/PMI.2016.6.823
Metallurgy and concentration
  • Date submitted
    2015-10-25
  • Date accepted
    2015-12-04
  • Date published
    2016-08-22

Regularities of selenium and chromium behavior in redox processes during hydrometallurgic treatment of solid phase products of rhenium extraction

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The main source of selenium is copper anode slime. But during the pyrometallurgical treatment of sulphide polymetallic ores significant amount of selenium along with radiogenic osmium and rhenium is concentrated in the solid-phase products of acid wash extraction and cannot be extracted, as gets lost with discharged chromium-containing solutions of osmium stage. The paper presents results of research into selenium reduction in the chromium-containing sulfuric acid medium by sulfurous gas and sodium sulphite. The use of the above reducers in optimum conditions leads to almost complete recovery of selenium (VI) while selenium (IV) extraction rate is not exceeding 60 %. The chrome (III) present in solutions has no impact on the selenium extraction rate. Chrome (VI) is almost completely reduced to a trivalent state, thus its negative impact on subsequent rhenium sorption from solutions purified from selenium is excluded. In view of a high rate of selenium extraction from chromium-containing sulfuric acid solutions formed in the process of radiogenic osmium production using sulfurous gas and sodium sulphite, choice of a method for selenium reduction is to a great extent dependent on the company’s profile.

How to cite: Petrov G.V., Kalashnikova M.I., Fokina S.B. Regularities of selenium and chromium behavior in redox processes during hydrometallurgic treatment of solid phase products of rhenium extraction // Journal of Mining Institute. 2016. Vol. 220 . p. 601-606. DOI: 10.18454/PMI.2016.4.601
Metallurgy and concentration
  • Date submitted
    2014-10-15
  • Date accepted
    2014-12-23
  • Date published
    2015-08-25

Nickel electrolyte purification from ferrum (III) and copper (II) impurities by extraction using a mixture of oleic acid and triethanolamine

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The conditions of the selective and joint extraction of copper and ferrum impurities from a nickel electrolyte by extraction using a mixture of oleic acid and trietanolamine in kerosene were determined: extraction Fe (III) at 3 < рН ≤ 4, 1 ≤ В:О ≤ 4 and t = 40 °C; extraction Cu (II) at 5 ≤ рН ≤ 6, 1 < В:О ≤ 4 and t = 40 °C; joint extraction of copper and ferrum at рН = 5-6, 1 ≤ В:О ≤ 4 and t = 40 °C. The process flow sheet of selective extraction of ferrum and copper from a nickel electrolyte by extraction using a mixture of oleic acid and triethanolamine in kerosene is given.

How to cite: Voropanova L.A., Kisiev N.T. Nickel electrolyte purification from ferrum (III) and copper (II) impurities by extraction using a mixture of oleic acid and triethanolamine // Journal of Mining Institute. 2015. Vol. 214 . p. 28-32.
Metallurgy and concentration
  • Date submitted
    2014-10-27
  • Date accepted
    2014-12-28
  • Date published
    2015-08-25

Extraction of rare earth metals of di-2-ethylhexyl phosphoric acid from phosphoric solutions

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The paper is devoted to solvent extraction of rare earth metals exemplified by Сe, Y from standard test and industrial solutions of wet-process phosphoric acid with di-2-ethylhexyl phosphoric acid used as extractant. The mechanism of rare earth metals extraction with di-2-ethylhexyl phosphoric acid was determined and studied on the basis of calculated thermodynamic characteristics. The paper considers the influence of impurity ions (Fe 3+ , Mg 2+ , ) on extraction of rare earth metals using industrial solutions. It has also been determined that for a stripping process the use of sulfuric acid solutions in concentration of 2 mol/l is the most preferable.

How to cite: Cheremisina O.V. Extraction of rare earth metals of di-2-ethylhexyl phosphoric acid from phosphoric solutions // Journal of Mining Institute. 2015. Vol. 214 . p. 39-50.
Metallurgy and concentration
  • Date submitted
    2014-09-18
  • Date accepted
    2014-11-15
  • Date published
    2015-06-26

Extraction of iron (III) ions from aqueous solutions with tributyl phosphate

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High rates of iron (III) ion extraction from aqueous solutions with tributyl phosphate by sequential injection of the extractant and minimal contact time of the solution and the extractant were obtained. The sequential injection of the extractant increases iron extraction and reduces the amount of the extractant used. The best extraction results were obtained from the solutions with concentration 3N HCl, 240 g/dm 3 NaCl and temperature t = 60 С. The flow sheet of the selective iron ions extraction from the aqueous solutions is presented.

How to cite: Voropanova L.A., Kokoeva N.B. Extraction of iron (III) ions from aqueous solutions with tributyl phosphate // Journal of Mining Institute. 2015. Vol. 213 . p. 24-30.
Oil and gas
  • Date submitted
    2014-07-21
  • Date accepted
    2014-09-19
  • Date published
    2014-12-22

Preliminary preparation of oil for primary processing

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Oil supplied for primary processing always undergoes preliminary preparation, the purpose of which is to eliminate the harmful effect of water and salt contained in the oil. It is thought that corrosion of the equipment is connected mainly with chlorides of magnesium and calcium, which are subjected to hydrolysis with the formation of hydrochloric acid. Under the influence of hydrochloric acid the destruction (corrosion) of metal equipment at technological plants occurs (especially refrigerating-condensing and heatexchange equipment, furnaces of rectification units etc.). The authors of the article, on the basis of thermodynamic calculations, provide their point of view on this process and give a methodology by which the process of preliminary oil dehydration and desalting can be controlled. The thermodynamic calculations executed for standard conditions on the basis of refer-enced data confirm a high probability of chemical interaction of iron with hydrogen ions, hy-drogen sulphide and especially with carbonic acid. This testifies to high activity of the carbon dioxide dissolved in water and the impossibility of hydrolysis of ions of magnesium, calcium and iron. The calculations show that only the hydrolysis of magnesium chloride is possible tak-ing into account the ionic composition of the water phase in the oil. It should be noted that the presence of ions of chlorine shifts the iron potential in a nega-tive direction and increases the speed of corrosion of petrochemical equipment. The solution of this problem is in the development of modern methods of crude oil dehydration and desalting. It is also, however, in an intensification of the processes of mixing water-oil emulsions with wash-ing water by using various physical fields (for example, ultrasound) and creating new effective mixing devices on the basis of them.

How to cite: Kondrasheva N.K., Dubovikov O.A., Ivanov I.I., Zyryanova O.V. Preliminary preparation of oil for primary processing // Journal of Mining Institute. 2014. Vol. 210 . p. 21-29.
Metallurgy
  • Date submitted
    2009-08-06
  • Date accepted
    2009-10-10
  • Date published
    2010-02-01

Allocation of tellurium from difficult on structure of sulfuric acid solutions

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As the main source of reception of tellurium serve electrolytic copper refinery slimes. In the conditions of manufacture expansion and transition on technology decopperizing slimes by pressure leaching O 2 -H 2 SO 4 media, the solution (decopperized product) becomes the basic concentrator of tellurium. Extraction of tellurium from a decopperized (pressure-leached) liquid products is considered. The method allows to raise percent of extraction of tellurium from initial raw materials and to enrich pressure-leached solid product with precious metals.

How to cite: Fokina S.B. Allocation of tellurium from difficult on structure of sulfuric acid solutions // Journal of Mining Institute. 2010. Vol. 186 . p. 207-209.