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Date submitted2024-06-17
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Date accepted2024-07-17
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Date published2025-04-25
Justification on the safe exploitation of closed coal warehouse by gas factor
The annual increase of coal production and its demand lead to the necessity in temporary storage places (warehouses) organization to accommodate raw coal materials before the shipment. It is noted that at the open method of coal storing the dust emission from loading/unloading operations and from the pile surface effects negatively the health of the warehouse workers and adjacent territories. An alternative solution is closed-type warehouses. One of the main hazards of such coal storage can be the release of residual methane from coal segregates into the air after degassing processes during mining and extraction to the surface, as well as transportation to the place of temporary storage. The study carries the analysis of methane content change in coal during the processes of extraction, transportation and storage. Physical and chemical bases of mass transfer during the interaction between gas-saturated coal mass and air are studied. It is determined that the intensity of methane emission depends on: the coal seam natural gas content, parameters of mass transfer between coal, and air and the ambient temperature. The dynamics of coal mass gas exchange with atmospheric air is evaluated by approximate approach, which is based on two interrelated iterations. The first one considers the formation of methane concentration fields in the air space of the bulk volume and the second accounts the methane emission from the pile surface to the outside air. It is determined that safety of closed coal warehouses exploitation by gas factor can be ensured by means of artificial ventilation providing volumetric methane concentration in the air less than 1 %. The flow rate sufficient to achieve this methane concentration was obtained as a result of computer modeling of methane concentration fields formation in the air medium at theoretically calculated methane emission from the pile surface.
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Date submitted2023-10-22
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Date accepted2024-03-05
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Date published2024-08-26
The mechanism and thermodynamics of ethyl alcohol sorption process on activated petroleum coke
The low-quality petcoke does not find qualified application and is stockpiled at refineries or used as solid fuel. One of the promising ways to use low-quality petroleum coke is its physical or chemical activation in order to obtain a highly porous carbon material that can be used as a catalyst carrier, adsorbent, base for electrodes, etc. The possibility of using petroleum coke to produce sorbent for organic compounds was studied. The activated petroleum cake was obtained by chemical activation with KOH, a specific surface area is 1218 m2/g. Sorption of ethyl alcohol was studied at temperatures 285, 293 and 300 K. It is a physical process proceeding mainly in pores of activated petroleum coke, also sorption can be described as a reversible exothermic process. The effective Gibbs energy at a temperature of 293 K is –12.74 kJ/mol, the heat of sorption is –26.07 kJ/mol. The obtained data confirm that porous carbon material obtained from petroleum coke can be used as sorbent for ethanol at room temperature. For example, for adsorption of bioethanol from the effluent of the fermentation process or for purification of wastewater from organic compounds.
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Date submitted2024-05-06
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Date accepted2024-06-14
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Date published2024-07-04
Natural carbon matrices based on brown coal, humic acids and humine extracted from it for purification of aqueous solutions from low molecular weight organic impurities
Heterogeneous systems including natural carbon matrices in the solid phase and aqueous solutions of low molecular weight organic compounds with positive and negative variations from ideality in the liquid phase are considered. The technical characterization of the considered supramolecular ensembles on the basis of brown coal of the Kara-Keche deposit (Kyrgyzstan), humic acids and humine extracted from it is given. Functional analysis of the samples was carried out using FTIR spectroscopy. The morphology of the surface of the considered carbon matrices has been investigated, in different points of which the local microelement composition has been established. An X-ray phase analysis of Kara-Keche brown coal and humic acids and humine extracted from it was carried out. The isothermal adsorption of bipolar molecules of glycine and urea, neutral D-glucose from aqueous solutions on solid carbon sorbents has been studied. An assumption has been made about the adsorption of low molecular weight organic compounds from aqueous solutions on humine and Kara-Keche coal in irregularities and pores of the carbon matrix of sorbents, for humic acids – on surface reaction centers. Due to its developed pore structure and resistance to acids and alkalis, humine from Kara-Keche coal is recommended for the purification of industrial wastewater from low molecular weight organic ecotoxicants.
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Date submitted2024-04-09
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Date accepted2024-06-03
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Date published2024-07-04
Analysis of the geochemical barriers effectiveness as the basis for the use of nature-like water purification technologies
Nature-like technologies are being introduced into many human activities including mining wastewater treatment. This work is based on long-term studies of the Sibay copper-zinc-pyrite deposit development. It is dedicated to assessment of geochemical barriers effectiveness in Cu, Zn, Cd removal from water of the Karagayly River (receiving quarry and dump drainage water). The research is based on the elements’ content and forms in water and bottom sediments, pH values etc. Four types of hydrogeochemical environment (formed due to changes in the water use over the past 20 years) were distinguished using discriminant analysis. The mechanisms of barriers formation and destruction were described. Statistical modeling of the metals’ precipitation was performed by multivariate regression analysis. Cu is adsorbed by recently formed Fe hydroxides, and, to a lesser extent, precipitates with sulfates as water pH increases. Antagonism to Mn hydroxides has been demonstrated, due to different physicochemical conditions for their precipitation. Zn enters solid phase mainly with sulfates, this element also forms its own mineral phases. The second mechanism is adsorption by recently formed Mn hydroxides, which corresponds to the idea of similar conditions for the precipitation of metal hydroxides. Cd behavior reflects conditions intermediate between these of Cu and Zn. Contribution of both mechanisms (related to Fe hydroxides and aqueous sulfates) is equal. Antagonism to Mn is absent. According to the assessment results using of nature-like technologies in situ in watercourses, canals and other water drainage systems is promising. Developed statistical models can be used for needs of experimental studies and artificial geochemical barriers engineering.
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Date submitted2023-04-11
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Date accepted2023-10-25
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Date published2024-07-04
Acid mine water treatment using neutralizer with adsorbent material
One of the biggest issues in the mining sector is due to acid mine drainage, especially in those abandoned mining operations and active ones that fail to adequately control the quality of their water discharge. The removal degree of copper, iron, lead, and zinc dissolved metals in acid mine drainage was investigated by applying different proportions of mixtures based on neutralizing reagent hydrated lime at 67 % calcium oxide (CaO), with adsorbent material – natural sodium bentonite, compared to the application of neutralizing reagent without mixing, commonly used in the neutralization of acid mining drainage. The obtained results show that the removal degree of dissolved metals in acid mine drainage when treated with a mixture of neutralizing reagent and adsorbent material in a certain proportion, reaches discharge quality, complying with the environmental standard (Maximum Permissible Limit), at a lower pH than when neutralizing material is applied without mixing, registering a net decrease in the consumption unit of neutralizing agent express on 1 kg/m3 of acid mine drainage. Furthermore, the sludge produced in the treatment with a mixture of the neutralizing reagent with adsorbent material has better characteristics than common sludge without bentonite, since it is more suitable for use as cover material, reducing the surface infiltration degree of water into the applied deposit.
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Date submitted2023-07-07
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Date accepted2023-09-20
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Date published2024-02-29
Isotherm and kinetic adsorption of rice husk particles as a model adsorbent for solving issues in the sustainable gold mining environment from mercury leaching
One of the techniques used in extracting gold in small-scale gold mining is mercury amalgamation. However, the use of mercury presents significant health and environmental hazards, as well as suboptimal efficiency in gold extraction. This study explores the possibility of the use of rice husk as a prototype adsorbent for mercury removal from its leaching in mining environments. To support the analysis, the rice husk adsorbent was characterized by Fourier-transform infrared spectroscopy, scanning electron microscopy, electron dispersive X-ray spectroscopy, atomic absorption spectrophotometers and Brunauer − Emmett − Teller analysis. To investigate the removal of Hg from aqueous solutions, batch adsorption experiments were conducted, and the efficiency was optimized under various parameters such as contact time, rice husk dosage, and initial concentration of mercury. Kinetic and isotherm investigations were also carried out to gain a better understanding of the adsorption properties. The kinetic adsorption was analyzed using the pseudo-first-order and pseudo-second-order. Furthermore, the isotherm adsorption was analyzed using ten adsorption isotherm models (i.e., Langmuir, Freundlich, Temkin, Dubinin – Radushkevich, Flory – Huggins, Fowler – Guggenheim, Hill – de Boer, Jovanovic, Harkin – Jura, and Halsey). The amount of mercury absorption increased with increasing contact time, adsorbent mass, and initial concentration of mercury. The pseudo-second-order kinetic model is the best model that can be applied to describe the adsorption process. Analysis of the adsorption results obtained shows that the adsorption pattern is explained through the formation of a monolayer without any lateral interaction between the adsorbate and adsorbent. In addition, the formation of multilayers due to inhomogeneous pore distribution also occurs which causes a pore filling mechanism. We found that the isotherm phenomena are near the Jovanovic models with the maximum adsorption capacity) of rice husk found to be 107.299 mg/g. As a result, rice husk could be a promising option for wastewater treatment due to its fast and efficient removal capacity, as well as its affordability and eco-friendliness. The predicted thermodynamic studies using the Flory – Huggins isotherm model show that the adsorption process is endothermic, spontaneous, and physisorption. The impact shows that the utilization of rice husk can be used and fit for the current issues in the sustainable development goals (SDGs).
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Date submitted2022-10-23
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Date accepted2023-02-13
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Date published2023-12-25
Sorption purification of acid storage facility water from iron and titanium on organic polymeric materials
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.
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Date submitted2022-01-24
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Date accepted2022-04-26
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Date published2023-04-25
Forecast of radionuclide migration in groundwater of the zone affected by construction drainage at the Leningrad NPP-2
The distribution of natural (at the level of global background) and technogenic radionuclides in groundwater of the industrial zone in Sosnovy Bor town, where several nuclear power facilities are operating, was analyzed. The main technogenic radionuclides recorded in groundwater samples are cesium ( 137 Cs), strontium ( 90 Sr), and tritium isotopes. The first two aquifers from the surface are subject to contamination: the Quaternary and the upper zone of the Lomonosov aquifer. Based on extensive material on the engineering and geological studies of the work area, a 3D geological model and hydrodynamic and geomigration models of the industrial zone were constructed. By means of modeling, the extent and nature of changes in hydrogeological conditions of area resulting from the construction and operational drainage of the new stage of the Leningrad Nuclear Power Plant (LNPP-2) were determined. The “historical” halo of radioactive contamination of groundwater forming (1970-1990) at the site adjacent to the NPP, where the storage facility of low- and medium-level radioactive waste is located, falls into the zone of influence. Interpretation of monitoring data allowed obtaining the migration parameters for predictive estimates. Modeling has shown that during the time of the LNPP-2 operation there was no intake of contaminated water by the drainage system of the new power plant.
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Date submitted2021-06-15
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Date accepted2021-10-18
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Date published2021-12-16
Study on hydrometallurgical recovery of copper and rhenium in processing of substandard copper concentrates
- Authors:
- Denis S. Lutskiy
- Aleksander S. Ignatovich
Over the past decade, there has been a steady growth in demand for rare metals, with rhenium being one of the most highly demanded, but also one of the most expensive and difficult to obtain. The high demand for rhenium is due to its use as a key component of metallurgical alloys or as a component of catalysts used in the oil refining industry. The aggregate of facts causes profitability of processing of the rhenium-containing mineral resources, which also are the copper substandard concentrates obtained at processing of the Zhezkazgan sandstones. The study focuses on the processes of extraction of copper and sorption recovery of rhenium from solutions of ammonia leaching of copper substandard concentrates. Model solutions similar in the elemental composition to solutions of ammonia leaching solutions of copper substandard concentrates obtained during the processing of Zhezkazgan sandstones were used as an object of the study. The paper estimates extraction characteristics of copper recovery using LIX 84-I solution in kerosene, as well as sorption characteristics of the rhenium recovery process using the Purolite PPA100 anion exchanger. Based on the obtained characteristics the possibility of hydrometallurgical processing of ammonia leaching solutions of substandard copper-sulfide concentrates, and recovery of the obtained commercial products is shown.
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Date submitted2019-07-11
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Date accepted2019-09-11
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Date published2020-04-24
Research of lithium sorption by KU-2-8 cation exchanger from model solutions simulating geothermal fluids in the dynamic mode
- Authors:
- Tatiana P. Belova
- Tatiana I. Ratchina
The extraction of chemical compounds from hydromineral raw materials is currently a promising objective. The geothermal deposits in the Kamchatka Territory should be considered as possible sources of lithium, boron and other chemical compounds. Their economic efficiency is justified by the complexity of the use of resources of geothermal fluids. The article presents data obtained as a result of experimental studies of lithium sorption by KU-2-8 cation exchanger from model solutions that simulate geothermal fluids in the dynamic mode. It was shown that in the first phase of sorption, ion exchange results in the absorption of lithium and sodium ions by the hydrogen form of cation exchanger up to the degree of cation exchanger saturation by 78 %. After that, the displacement of lithium ions by sodium ions is observed. The intermediate solutions were obtained in which the molar ratio of Li/Na is 80 times higher than in the initial solution. To separate sodium and lithium, it is proposed to use the lithium form of cation exchanger obtained using a portion of lithium chloride concentrate. The separation occurs due to the displacement of lithium ions by sodium ions. The effluent has a molar ratio of Li/Na = 10.4. The regeneration is carried out with 1 n hydrochloric acid, while the concentration coefficient of sodium chloride equals three.
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Date submitted2019-06-02
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Date accepted2019-09-02
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Date published2020-04-24
Sorption of nickel (II) and manganese (II) ions from aqueous solutions
Mine water from non-ferrous metal deposits is often contaminated with nickel and manganese ions. The entry of these ions, especially nickel, into surface waters and underground aquifers is undesirable since it has a negative effect on living organisms and worsens the condition of drinking water sources. One of the promising methods for selectively extracting nickel ions and obtaining an eluate suitable for further use is sorption by weakly acid cation exchangers with chelate groups of iminodiacetic acid. As part of the study, sorption isotherms of nickel and manganese ions by Lewatit MonoPlus TP 207 cation exchanger in mono- and bicomponent systems were obtained. In monocomponent systems, the maximum static exchange capacity (SEC) of the cation exchanger for nickel ions is 952 mmol/dm 3 , and in bicomponent systems – 741 mmol/dm 3 ; for manganese ions– 71 mmol/dm 3 and 49 mmol/dm 3 , respectively. It is obvious that the studied cation exchanger has a greater capacity for nickel ions than for manganese ions. The influence of a temperature increase from 300 to 330 K on the sorption of nickel and manganese ions was established: in monocomponent systems, the maximum degree of extraction of the former increases from 65 to 77 % (SEC from 337 to 399 mmol/dm 3 ), and the latter from 21 to 35 % (SEC – from 140 to 229 mmol/dm 3 ); in bicomponent systems, the extraction of nickel ions increases from 59 to 78 % (SEC – from 307 to 429 mmol/dm 3 ), and manganese ions decreases from 20 to 17 % (SEC – from 164 to 131 mmol/dm 3 ). The predominant increase in the indicators is due to the filling of the sorption centers of the ion-exchange resins, which are energetically unfavorable for the exchange of counterions at a lower temperature. The influence of the pH of the solution on sorption was determined: the intensification of the process for nickel ions is observed in the pH range of 8.0-8.5 in a monocomponent solution and 8.0-9.0 in a bicomponent solution, for manganese ions in the range of 8.0-9.5 in both cases. The increase in the degree of extraction of ions and the exchange capacity of the ion exchanger with increasing pH is associated with the appearance of singly charged hydroxocations, dissociation of the functional groups of the sorbent and, to some extent, with the subsequent formation of insoluble forms of nickel and manganese. However, with increasing pH, a decrease in the selectivity of nickel extraction is observed: the ion separation coefficient decreases from 14.0 to 6.0 in the pH range of 6.0-11.0.
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Date submitted2019-05-02
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Date accepted2019-07-09
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Date published2019-10-23
Effect of Temperature on Solid-state Hydride Metal Synthesis According to Thermodynamic Modeling
Thermodynamic modeling of the reduction of copper dichloride in the media of various gaseous hydrides (ammonia, monosilane, methane) in the temperature range 273-1000 K was carried out. Calculations show that in narrower temperature ranges corresponding to the reactions of solid-state hydride synthesis (SHS) of metal sub- stances metal formation is usually supported by theoretical propositions. As a result of thermodynamic modeling, a principal result was obtained on the suppression of competing processes of nitriding, siliconizing and carbonization of metal under SHS conditions, which is important for metallurgical production. This additionally substantiates the correctness of previous experimental studies of SHS metals with modified surface and improved properties. By mod- eling, it was found that the reduction of solid copper dichloride to metal in ammonia or methane occurs stepwise (se- quentially, according to the Baykov rule) through the intermediate stages of the formation of a compound of low- valent copper – copper (I)chloride.
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Date submitted2019-03-05
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Date accepted2019-05-03
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Date published2019-08-23
Efficiency Estimation of the Single- and Multicomponent Anti-hydrate Reagents
- Authors:
- N. A. Shostak
- E. P. Zaporozhets
Different types of technological and technical problems in the oil, gas and chemical industries are connected with the hydrate formation process and with the using of anti-hydrate chemicals. That is why, it is necessary to estimate thermobaric ranges within which reagents does not let hydrate to grow or is their dissociation. Also, to estimate anti-hydrate influence we need to determine the chemicals’ anti-hydrate efficiency and chose the best one. They make the reagents consisting of several chemical components depending on the purpose of their application – for prevention of formation and (or) elimination of hydrates. It demands calculations of the optimum concentration and expenses and also the intensity (speed) of hydrates dissociation causing with the reagents. The analytical method of the anti-hydrate chemical reagents efficiency determination containing one or several components from different classes of chemical compounds – alcohols, salts, acids, compounds of nitrogen and oxygen – is presented in this paper. With its help it is possible to define decrease in temperature of hydrate formation from reagents influence, to count key parameters of reagents anti-hydrate efficiency depending on component compositions of hydrate gas and a phase condition of a hydrate-gas system, to select types of chemical components and their quantity in multicomponent reagents, i.e., to make new compounds. The method can be used for express assessment of anti-hydrate chemical reagents efficiency on criteria sign for practical application in oil, gas and processing industry.
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Date submitted2016-08-30
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Date accepted2016-10-30
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Date published2017-02-22
Gas-dynamic processes affecting coal mine radon hazard
- Authors:
- V. I. Efimov
- A. B. Zhabin
- G. V. Stas
The paper focuses on vertical migration of radon in surrounding rocks described by Fick's first law as well as by the continuity equation for diffusion flow, with allowance for sorption and radioactive decay processes. Taking into account special characteristics of vertical radon diffusion, the process can be considered stable. It is demonstrated that for productive areas it is feasible to consider one-dimensional convective diffusion, as diffusive transport of radon by the air of productive areas occurs at steady-state conditions. Normally the factor of radon emissions prevails if atmospheric pressure is constant. Amount of air, calculated using this factor, by 20-30 % exceeds the one needed to dilute carbon dioxide to maximum allowed concentration (MAC).
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Date submitted2009-08-27
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Date accepted2009-10-25
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Date published2010-02-01
Regularities of change of water-repellent properties of the nanostructured metal powders on the base of aluminium
Regularities of change of water-repellent properties of metal powders on the basis of aluminium depending on the program of nano-structural surface modifying are studyed. The rows of increase of water-repellent properties of modified aluminium on the base of coarse-dispersed and high-dispersed (PAP-2) powders are obtained. Several specimens excelling initial hydrohobic PAP-2 inits water-repellent capacity are found out. The research uses the methods of XP-, EDX- spectroscopy and gravimetry.
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Date submitted2008-10-30
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Date accepted2008-12-22
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Date published2009-12-11
Investigations of the mechanism of methane desorption in coal saturation with carbon dioxide
- Authors:
- A. T. Karmansky
The article considers the developed unit for investigations of interaction between coal and gas, and gas outflow from the coal surface by gravimetric method under gas pressure up to 6 MPa. Relationship between the sorption ability and metamorphism stage is explained by the microstructure of coal. The adsorption increment indices of volume V and velocity of changes in pressure P – during adsorption may be used for prediction of outburst-hazard of coal and gas.