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EN
In this work, the processes of purification of oily waters using magnetites were investigated: magnetite synthesized according to the classical method and magnetites modified with hydrophobizing agents (sulfonol or alkylimidazolin). It was shown that magnetite modified with alkylimidazolin in doses of 50–200 mg/dm3 provides a high degree of oil removal from waters of various mineralization. The degree of water purification reaches 97.5–99.8%. Sulfonol-modified magnetite shows greater efficiency than conventional magnetite only at high concentrations (200 mg/dm3) and only in fresh water. Three hours is enough to ensure the maximum degree of purification of water-oil solutions. Changing the amount of hydrophobizing agent (alkylimidazolin) during the synthesis of magnetite reduces the effect of pH on the purification of both fresh and mineralized waters.
EN
The article describes the modern problems of formation and purification of marine oil-containing waters. The efficiency of using electrocoagulation to remove oil from water-oil emulsions of different mineralization using aluminum and iron anodes was studied. Treatment of water-oil solutions with an oil content of 100 mg/dm3 by electrocoagulation in a single-chamber electrolyzer provides 98–99% oil removal using these electrodes at an anode current density of 0.57–2.11 A/dm2 for highly mineralized waters and 0.34 A/dm2 for freshwater treatment during the first 15 minutes provides a reduction in oil concentration from 100 mg/dm3 to values at the level of 1.55–2.93 mg/dm3. When the water treatment time is extended to 45 minutes, greater efficiency in highly mineralized waters is provided by the aluminum anode.
EN
Processes of water purification from phosphates using a low-pressure reverse osmosis membrane were studied. It was shown that the concentration of phosphates in the permeate largely depends on their initial concentration in the water and increases along with the degree of permeate selection. It was established that when using the Filmtec TW3–1812–50 membrane for phosphate concentrations up to 20 mg/dm3, their concentration in the permeate does not exceed 2.5 mg/dm3 with a degree of permeate selection up to 90% when cleaning solutions in distilled and artesian water. This value is below the permissible level for drinking water. When the concentration of phosphates increases to 100 and 1000 mg/dm3, their content in the permeate increases sharply to the values significantly higher than the permissible level in both drinking and wastewater. When sodium orthophosphate was added to artesian water, the effectiveness of its purification on this membrane with respect to chlorides, sulfates, hardness ions, and hydrocarbons was high. This indicates that the cartridges with these membranes can be used both in industrial installations and in households for further purification of artesian and tap water to drinking water quality.
4
Content available Alternative Ways of Extracting Oil from Water Bodies
EN
The article compares the use of sorption and sorption-coagulation methods for cleaning fresh and mineralized oil-containing waters. The sorbents used are thermally expanded graphite obtained by heat treatment of graphite bisulfate in a boiling layer, and activated carbon of BAU-A grade, which is widely used for purification of liquid media from oils and oil products. As an alternative to the sorption method, research was conducted on the application of the sorption-coagulation method with the simultaneous use of aluminum-containing coagulants: aluminum sulfate and aluminum hydroxochloride and activated carbon. It is shown that the advantages of using the sorption method using thermally expanded graphite are based on the high efficiency of oil extraction from water bodies and multiple regeneration of the spent sorbent.
EN
The processes of water purification with increasing selection of permeate were studied, considering selectivity and productivity of membranes, dynamics of changes of contents of components in the concentrate. It is shown that when chlorides and sulfates are removed from water, the increase in their content in the concentrate does not differ practically from the measured and calculated values. At the same time, the nature of dependences on the change in hardness, concentration of calcium and magnesium ions, alkalinity obtained experimentally differ significantly from the dependences obtained by theoretical calculations at permeate selection levels of > 70%. А significant difference in the determined and calculated concentrations of hardness ions in the concentrates was observed after hardness values greater than 30–40 mg-eq/dm3. This indicates the partial removal of hardness ions and carbonates from the concentrates, which may be the reason for the formation of deposits on the membrane. Permissible values of the degree of permeate selection were determined, at which there is no intense deposition of carbonates and hydroxides of hardness ions on the membrane. With the initial water hardness > 8 mg-eq/dm3, the degree of permeate selection could reach 60–70% without the risk of sedimentation on the membrane. Effectiveness of the low-pressure reverse osmosis membrane in the purification of mine water with an increased level of mineralization and hardness was determined. A significant difference between the determined and calculated hardness in concentration was observed already at the degree of permeate selection of 22–33%.
EN
The results of electrochemical processing of spent acidic, neutral, and alkaline sulfate-chloride-containing regenerative solutions in two- and three-chamber electrolyzers are presented. It has been determined that the highest current efficiency for the products of electrodialysis can be achieved in the presence of hardness ions when processing acidic sulfate-containing solutions using three-chamber electrolyzers. It has been established that during electrodialysis of alkaline solutions after regeneration of anionites containing chloride ions, accumulation of alkali occurs in the cathodic region, and in the anodic region, chloride ions accumulate due to diffusion through the anion exchange membrane during the first stage, followed by preferential oxidation of chloride ions with liberation of free chlorine during the second stage. It has been shown that electrodialysis can effectively solve the problem of comprehensive processing of neutral, alkaline, and acidic regenerative sulfate-chloride-containing solutions, with the production of alkali and acid at concentrations suitable for reuse in regeneration processes.
EN
The process of extracting nitrates from water by the methods of reverse osmosis and ion exchange was investigated in the paper. In the formation of reverse osmosis, low-pressure membranes were used, and in ion-exchange processes, highly alkaline anionite AB–17–8 was applied in salt form. The dynamics of changes in the concentration of nitrates in the permeate and the concentration with an increase in the degree of permeate selection from 9 to 90% at initial nitrate concentrations of 18, 50 and 100 mg/dm3 were determined. The indicators of selectivity and productivity of membranes were calculated depending on the degree of permeate selection. It was shown that the low-pressure reverse osmosis membrane is characterized by low selectivity values at high productivity values in the selected part of the nitrate concentration. It was established that the ion exchange method is significantly more effective than reverse osmosis in removing nitrates from water. It ensures the reduction of nitrate content in purified water to a value of less than 1 mg/dm3 when the degree of their extraction is reached at the level of 99%. As the ionite is saturated with nitrates, the efficiency of their extraction decreases. Anionite sorbs nitrates effectively enough, being both in the chloride mixture and in the sulfate form. Nitrates are effectively desorbed by 2H solutions of sodium chloride and sodium or ammonium sulfate.
EN
The analysis of water conditioning methods for closed water supply systems was carried out in the work. The expediency of using redoxites based on ion exchange materials to combat the corrosion processes in water recirculation systems by preliminary deoxidation of water was shown. Modified KU-2–8, Dowex Mac-3, AB-17–8, Dowex Marathon WBA, AMBERLITE IRA 96 ion exchange resins were used as deoxidizing materials.
EN
The necessity of development of technical solutions that will allow to reduce carbon monoxide emissions of flue gases of industrial productions is substantiated. It is shown that the most rational design solution to the problem of carbon monoxide pollution during the firing of electrode blanks is the use of aerated concrete blocks with a catalyst, which can be quickly and conveniently located directly on the carbon material of the “green” electrodes pouring in the subfloor space of the firing furnaces. Modified by oxides of Mn4+, Fe2+, Fe3+, Cu2+, Cr3+ -catalysts based on aerated concrete were obtained. It is shown that in an empty reactor in the temperature range 200–400 °С the degree of conversion of carbon monoxide in the absence of a catalyst is zero. It is established that on the investigated catalysts based on aerated concrete 100% oxidation of carbon monoxide is achieved at a temperature of 390 °C in the case of using a mixture of catalyst powders 30% CuO + 70% MnO2, 40% CuO + 60% MnO2, 50% Fe (FexCr1-x) 2O4 + 50% MnO2; 50% Fe3O4 + 50 % MnO2. It is determined that the addition of ferrite catalyst powder in aerated concrete in a mixture or without manganese dioxide does not critically affect the mechanical properties of the products.
EN
The processes of manganese (II) ions removal from water using sorbent catalysts and ion exchange materials modified with iron oxides were studied. It was shown that manganese ions oxidize very slowly in artesian water, even when the pH is adjusted to 9.0. Intensive aeration of solutions due to stirring also does not promote the oxidation of manganese (II) ions. The degree of manganese extraction due to oxidation is reduced from 20–30% for solutions with a concentration of manganese ions of 1 and 5 mg/dm3 to 11–15% for solutions with a concentration of 15 and 30 mg/dm3. A significant increase in the oxidation efficiency of manganese ions was achieved by using magnetite as a sorbent catalyst. The efficiency of water demanganization increases along with the intensity of water aeration when mixing solutions. It was established that strongly acid cation exchangers provide efficient extraction of manganese ions from water. At the same time, a high exchange capacity of strong acid cation exchange resin KU-2–8 in acid and salt form was noted. It was shown that the capacity of manganese ions of this cation exchange resin in the Ca2+-form is slightly lower. When using the KU-2–8 in Ca2+-form of cation exchange resin to remove manganese ions from the solution already in the first samples, the leakage of manganese ions at the level of 10 mg/dm3 and above was observed. This indicates that this form of ion exchanger is not suitable for deep purification of water from manganese (II) ions. In order to increase the efficiency of manganese ion extraction from water, increase the duration of the filter cycle, magnetite and magnetite-modified KU-2–8 cation exchange resin were used as a sorbent-catalyst. It was shown that the cation exchange resin modified with magnetite provides the removal of a significant part of manganese ions due to catalytic oxidation on magnetite. The conditions of effective manganese extraction under static and dynamic conditions are determined.
EN
In this work, the process of water deironing by using magnetite as a catalyst to accelerate the oxidation of iron ions in an aqueous medium was investigated. It was shown that the efficiency of iron ion extraction depends on the solution concentration, sorbent dose and contact time. In all cases, the use of magnetite accelerated the process of extraction of iron by more than an order of magnitude in comparison with similar experiments on the oxidation of iron without the addition of a catalyst. At the pH values greater than 6, the use of magnetite as a catalyst contributes to the deep purification of water from iron ions.
EN
In this work, the processes of electrochemical processing of sodium chloride solutions with the production of iron (III) chloride and alkali in a three-chamber electrolyzer with MA-41 anion-exchange membrane and MK-40 cation-exchange membrane were investigated. The conditions for the removal of sodium chloride from water in a three-chamber electrolyzer using an iron anode were determined depending on the anode current density and the reaction of the medium in the anode region. The parameters of the process of concentrating iron chloride in the anode region were established at relatively low concentrations of sodium chloride solution. It was shown that during the electrolysis of a sodium chloride solution with a concentration of 370 mg-eq/dm3 at a current of 0.2 A in a three-chamber electrolyzer with an iron anode, an iron chloride solution is formed in the anolyte at pH < 4.9. The rate of concentration of NaOH to catholyte and FeCl3 to anolyte increased along with the current density. It was found that in order to increase the concentration of iron (III) chloride in the anolyte at relatively low concentrations of sodium chloride solution, it is advisable to gradually renew the demineralized solutions in the working chamber.
EN
The paper presents the results of the investigation on the efficiency of the potassium ferrate application in water conditioning processes: oxidation of pollutants of different composition by ferrate compounds; clarification of model solutions by coagulation; reduction of corrosive aggressiveness of aqueous solutions. The optimal conditions for the water clarification process using potassium ferrate were: reagent dose 1 mg∙dm-3, pH close to neutral, and temperature 20°C. The oxidation rate of organic substances by the potassium ferrate solutions was 50% when applied in concentrations of 15-20 mg∙dm-3. The studies on the possible application of the reagent as a steel corrosion inhibitor in neutral aqueous media were conducted. The degree of corrosion protection reached 60%, which indicated the prospect of using iron (VI) compounds as inhibitory additives.
EN
In this study, the processes of electrochemical oxidation of ammonia in a two-chamber electrolyzer with anion exchange membrane MA-41 were investigated. An estimation of the efficiency of the process of oxidation of ammonia, depending on the chemical composition of the initial solution of anolyte and catholyte, current density and time of electrolysis was carried out. It was shown that the oxidation of ammonia in the anode chamber passes quickly and is accompanied by a significant decrease in pH due to the formation of nitrogen dioxide and nitrates. At the same time, the current output and the electrical conductivity of the dilute solutions was rather low. The effect of chlorides on the process of electrolysis was investigated. It was shown that the presence of chlorides in the anolyte catalyzes the processes of oxidation of ammonia. An increase in the concentration of chlorides in the anolyte increases output and reduces electricity consumption. The presence of chlorides in the catholyte does not accelerate oxidation. The presence of sulfates, both in the anolyte and in the catholyte, slows down the process of oxidation of ammonia as a result of the oxidation of sulfates to persulfates, which are quite passive to ammonium ions. At the same time, electricity consumption increases.
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