Albert Zh. Kaltaev
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The organizations/institutes from the scholar's latest article
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Albert Zh. Kaltaev has a total of 50 co-authors. Here are the top co-authors by number of shared publications:
- Kirill Borisovich Larionov
National Research Tomsk Polytechnic University, Tomsk, Russia
13 shared publications - Александр Сергеевич Горшков
Tomsk Polytechnic University, Tomsk, Russia
7 shared publications - Konstantin Vitalievich Slyusarskiy
Tomsk Polytechnic University, Tomsk, Russia
5 shared publications - A. V. Gubin
School of Energy & Power Engineering, National Research Tomsk Polytechnic University, 634050 Tomsk, Russia
2 shared publications - Andrey V. Zenkov
National Research Tomsk Polytechnic University
2 shared publications - Berezikov Nikolay
Tomsk Polytechnic University, Tomsk, Russia
2 shared publications
Latest Publications
- Open Access
- 2 July 2026
- Published by Elsevier in SSRN Electronic Journal
Synthesis of high-entropy diborides (TiZrHfTaMo)B2, (TiZrHfMoW)B2 and (TiZrHfTaW)B2 by open-air DC arc plasma: comparative study of Mo vs. W on structure, microstructure, photocatalytic and electrocatalytic activity
High-entropy diborides (TiZrHfTaMo)B2, (TiZrHfMoW)B2 and (TiZrHfTaW)B2 were synthesised for the first time using a three-electrode DC arc reactor in open air. Replacing Mo with W increases crystallite size of the high-entropy phase from 30 to 48 nm, reduces microstrains, but promotes a secondary W2B5 phase. Specific surface area rises from 0.116 to 0.96 m2/g, forming a mesoporous structure. In betulin oxidation, (TiZrHfTaMo)B2 shows conversions of 5.34 % (dark) and 6.45 % under UV(420 nm) with up to 19.6 % selectivity to betulinic acid, while W-containing samples are less active and exhibit no photocatalysis. For the hydrogen evolution reaction, (TiZrHfMoW)B2 delivers the best performance: overpotentials η10 of 642 mV (0.5 M H2SO4) and 510 mV (1 M KOH), and Tafel slopes of 208 and 226 mV/dec. These findings demonstrate that replacing Mo with W tunes the microstructure and properties of high-entropy borides, making (TiZrHfMoW)B2 a promising non-precious electrocatalyst for hydrogen production.
- 2 July 2026
- Published by Elsevier in SSRN Electronic Journal
Open AccessSynthesis of high-entropy diborides (TiZrHfTaMo)B2, (TiZrHfMoW)B2 and (TiZrHfTaW)B2 by open-air DC arc plasma: comparative study of Mo vs. W on structure, microstructure, photocatalytic and electrocatalytic activity
High-entropy diborides (TiZrHfTaMo)B2, (TiZrHfMoW)B2 and (TiZrHfTaW)B2 were synthesised for the first time using a three-electrode DC arc reactor in open air. Replacing Mo with W increases crystallite size of the high-entropy phase from 30 to 48 nm, reduces microstrains, but promotes a secondary W2B5 phase. Specific surface area rises from 0.116 to 0.96 m2/g, forming a mesoporous structure. In betulin oxidation, (TiZrHfTaMo)B2 shows conversions of 5.34 % (dark) and 6.45 % under UV(420 nm) with up to 19.6 % selectivity to betulinic acid, while W-containing samples are less active and exhibit no photocatalysis. For the hydrogen evolution reaction, (TiZrHfMoW)B2 delivers the best performance: overpotentials η10 of 642 mV (0.5 M H2SO4) and 510 mV (1 M KOH), and Tafel slopes of 208 and 226 mV/dec. These findings demonstrate that replacing Mo with W tunes the microstructure and properties of high-entropy borides, making (TiZrHfMoW)B2 a promising non-precious electrocatalyst for hydrogen production.
- Open Access
- 18 April 2026
- Published by Elsevier in SSRN Electronic Journal
Co-combustion of high-moisture coal tar and waste tire pyrolysis oil
High-moisture coal tar is a challenging fuel for energy utilization due to difficulties in ensuring its stable combustion and its low calorific value. One promising solution is its co-combustion with energy-rich pyrolysis oil derived from waste tires. To the best of our knowledge, the synergistic effect and chemical interactions during the co-combustion of high-moisture coal tar and waste tire pyrolysis oil have not been investigated previously. It has been experimentally established that the addition of high-moisture coal tar to waste tire pyrolysis oil enhances its reactivity, which is reflected in a reduction of ignition delay time. Using comparative experiments with acetic acid and ethanol, it was confirmed that chemical interactions between oxygenated components of the tar and hydrocarbons of the tire-derived pyrolysis oil play a decisive role in enhancing fuel reactivity. It was also found that increasing the mass fraction of tar in the fuel blend reduces CO and NOx emissions.
- 18 April 2026
- Published by Elsevier in SSRN Electronic Journal
Open AccessCo-combustion of high-moisture coal tar and waste tire pyrolysis oil
High-moisture coal tar is a challenging fuel for energy utilization due to difficulties in ensuring its stable combustion and its low calorific value. One promising solution is its co-combustion with energy-rich pyrolysis oil derived from waste tires. To the best of our knowledge, the synergistic effect and chemical interactions during the co-combustion of high-moisture coal tar and waste tire pyrolysis oil have not been investigated previously. It has been experimentally established that the addition of high-moisture coal tar to waste tire pyrolysis oil enhances its reactivity, which is reflected in a reduction of ignition delay time. Using comparative experiments with acetic acid and ethanol, it was confirmed that chemical interactions between oxygenated components of the tar and hydrocarbons of the tire-derived pyrolysis oil play a decisive role in enhancing fuel reactivity. It was also found that increasing the mass fraction of tar in the fuel blend reduces CO and NOx emissions.
- 30 January 2025
- Published by Elsevier in Biomass and Bioenergy
- Vol. 194
Plasma gasification of frying oil to produce hydrogen-rich synthesis gas and nanodispersed carbon material
- 30 January 2025
- Published by Elsevier in Biomass and Bioenergy
- Vol. 194
Plasma gasification of frying oil to produce hydrogen-rich synthesis gas and nanodispersed carbon material
- 1 January 2025
- Published by Allerton Press in Coke and Chemistry
- Vol. 68 (1) , 35-44
Combustion of Petroleum Coke with Pyrolytic Residue from Scrap Tires
The possibility of using petroleum coke and the pyrolytic carbon residue from scrap tires as a mixed fuel is considered. The influence of the coke/residue
- 1 January 2025
- Published by Allerton Press in Coke and Chemistry
- Vol. 68 (1) , 35-44
Combustion of Petroleum Coke with Pyrolytic Residue from Scrap Tires
The possibility of using petroleum coke and the pyrolytic carbon residue from scrap tires as a mixed fuel is considered. The influence of the coke/residue
- 21 October 2024
- Published by The Russian Academy of Sciences in Химия твердого топлива
- No. 3,p. 59-66
Activation of the process of layer combustion of bitter coal with iron nitrate and waste of metal rolling production
The influence of metal-rolling production waste and iron nitrate on the characteristics of the process of layer combustion of coal is investigated. As a solid fuel, coal of the T grade was used. Metal scale and iron nitrate were introduced into the fuel by mechanical mixing. According to XRD data, phases of iron oxides Fe3O4 and manganese Mn3O4 were identified in the metal scale. The characteristics of the combustion process of the studied samples were studied using high-speed video with the use of a combustion chamber at a heating medium temperature of 700°C. Combustion Also, the process of activated layer combustion coal was scaled using a solid fuel boiler unit. It has been experimentally established that the use of metal scale and iron nitrate leads to an increase in the reactivity of the fuel, as evidenced by a decrease in the ignition delay time. Due to the intensification of the combustion process, the fuel underburning and the concentration of CO formed in the composition of gas-phase combustion products were reduced.
- 21 October 2024
- Published by The Russian Academy of Sciences in Химия твердого топлива
- No. 3,p. 59-66
Activation of the process of layer combustion of bitter coal with iron nitrate and waste of metal rolling production
The influence of metal-rolling production waste and iron nitrate on the characteristics of the process of layer combustion of coal is investigated. As a solid fuel, coal of the T grade was used. Metal scale and iron nitrate were introduced into the fuel by mechanical mixing. According to XRD data, phases of iron oxides Fe3O4 and manganese Mn3O4 were identified in the metal scale. The characteristics of the combustion process of the studied samples were studied using high-speed video with the use of a combustion chamber at a heating medium temperature of 700°C. Combustion Also, the process of activated layer combustion coal was scaled using a solid fuel boiler unit. It has been experimentally established that the use of metal scale and iron nitrate leads to an increase in the reactivity of the fuel, as evidenced by a decrease in the ignition delay time. Due to the intensification of the combustion process, the fuel underburning and the concentration of CO formed in the composition of gas-phase combustion products were reduced.
- 5 June 2024
- Published by Allerton Press in Solid Fuel Chemistry
- Vol. 58 (3) , 219-225
Activation of the Process of Layer Combustion of Coal with Iron Nitrate and Waste of Metal Rolling Production
The influence of metal-rolling production waste and iron nitrate on the characteristics of the process of layer combustion of coal was investigated. Coal o
- 5 June 2024
- Published by Allerton Press in Solid Fuel Chemistry
- Vol. 58 (3) , 219-225
Activation of the Process of Layer Combustion of Coal with Iron Nitrate and Waste of Metal Rolling Production
The influence of metal-rolling production waste and iron nitrate on the characteristics of the process of layer combustion of coal was investigated. Coal o
- 1 June 2024
- Published by American Society of Civil Engineers (ASCE) in Journal of Energy Engineering
- Vol. 150 (3)
Cocombustion of Coal–Water Fuel with Fuel Oil
- 1 June 2024
- Published by American Society of Civil Engineers (ASCE) in Journal of Energy Engineering
- Vol. 150 (3)
Cocombustion of Coal–Water Fuel with Fuel Oil
- Open Access
Ignition and Emission Characteristics of Waste Tires Pyrolysis Char Co-Combustion with Peat and Sawdust
The pyrolysis processing of waste tires is a promising technology for obtaining products with high marginality. One of the possible methods of solid pyrolysis product utilization is its combustion for energy production, but this is complicated by poor reactivity and sulfur emissions. The combustion of char together with more reactive fuels could solve this problem. The current study is devoted to the combustion characteristics of waste tires pyrolysis carbon residue mixed with biomass: pine sawdust and peat. The oxidation characteristics in thermal analyzer conditions were found to change insignificantly. In contrast, 15 wt% of peat and sawdust additives was found to decrease ignition delay times in realistic conditions of combustion at 800 °C by 42 and 78%, respectively, while the SO2 emissions also dropped by 73 and 52%, respectively. The extra sulfur was found to be contained in ash residue in the form of CaS and CaSO4. While increasing peat concentration from 5 to 15 wt% was found to have almost no effect, the same increase for sawdust resulted into an almost proportional decrease in ignition delay times. The results obtained could be used for the integration of waste tires pyrolysis char mixtures with peat or sawdust into the energy sector.
Open AccessIgnition and Emission Characteristics of Waste Tires Pyrolysis Char Co-Combustion with Peat and Sawdust
The pyrolysis processing of waste tires is a promising technology for obtaining products with high marginality. One of the possible methods of solid pyrolysis product utilization is its combustion for energy production, but this is complicated by poor reactivity and sulfur emissions. The combustion of char together with more reactive fuels could solve this problem. The current study is devoted to the combustion characteristics of waste tires pyrolysis carbon residue mixed with biomass: pine sawdust and peat. The oxidation characteristics in thermal analyzer conditions were found to change insignificantly. In contrast, 15 wt% of peat and sawdust additives was found to decrease ignition delay times in realistic conditions of combustion at 800 °C by 42 and 78%, respectively, while the SO2 emissions also dropped by 73 and 52%, respectively. The extra sulfur was found to be contained in ash residue in the form of CaS and CaSO4. While increasing peat concentration from 5 to 15 wt% was found to have almost no effect, the same increase for sawdust resulted into an almost proportional decrease in ignition delay times. The results obtained could be used for the integration of waste tires pyrolysis char mixtures with peat or sawdust into the energy sector.