Spasojević, Miroslav

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  • Spasojević, Miroslav (9)
Projects

Author's Bibliography

The effect of the composition of the alloy of RuO2 and Pt nanocrystals on intermediate adsorption during methanol oxidation

Spasojević, Milica; Ribić Zelenović, Lenka; Spasojević, Miroslav; Trišović, Tomislav

(Editura Academiei Romane, 2020)

TY  - JOUR
AU  - Spasojević, Milica
AU  - Ribić Zelenović, Lenka
AU  - Spasojević, Miroslav
AU  - Trišović, Tomislav
PY  - 2020
UR  - https://dais.sanu.ac.rs/123456789/10033
AB  - A catalytic coating composed of a mixture of RuO2 and Pt nanocrystals was prepared by a thermal procedure on a titanium substrate and used for the electrochemical oxidation of methanol. The adsorption of the intermediate CO, formed by methanol oxidation on Pt nanocrystals, depended on potential and the coating composition. An increase in the RuO2 content decreased the rate of methanol dehydrogenation and increased the rate of oxidation of the strongly bound intermediate COad. This caused a decrease in the maximum coverage of Pt nanocrystals with COad and a shift of the rapid linear drop in COad coverage to more negative potentials.
PB  - Editura Academiei Romane
T2  - Revue Roumaine de Chimie
T1  - The effect of the composition of the alloy of RuO2 and Pt nanocrystals on intermediate adsorption during methanol oxidation
SP  - 481
EP  - 489
VL  - 65
IS  - 5
DO  - 10.33224/rrch.2020.65.5.08
UR  - https://hdl.handle.net/21.15107/rcub_dais_10033
ER  - 
@article{
author = "Spasojević, Milica and Ribić Zelenović, Lenka and Spasojević, Miroslav and Trišović, Tomislav",
year = "2020",
abstract = "A catalytic coating composed of a mixture of RuO2 and Pt nanocrystals was prepared by a thermal procedure on a titanium substrate and used for the electrochemical oxidation of methanol. The adsorption of the intermediate CO, formed by methanol oxidation on Pt nanocrystals, depended on potential and the coating composition. An increase in the RuO2 content decreased the rate of methanol dehydrogenation and increased the rate of oxidation of the strongly bound intermediate COad. This caused a decrease in the maximum coverage of Pt nanocrystals with COad and a shift of the rapid linear drop in COad coverage to more negative potentials.",
publisher = "Editura Academiei Romane",
journal = "Revue Roumaine de Chimie",
title = "The effect of the composition of the alloy of RuO2 and Pt nanocrystals on intermediate adsorption during methanol oxidation",
pages = "481-489",
volume = "65",
number = "5",
doi = "10.33224/rrch.2020.65.5.08",
url = "https://hdl.handle.net/21.15107/rcub_dais_10033"
}
Spasojević, M., Ribić Zelenović, L., Spasojević, M.,& Trišović, T.. (2020). The effect of the composition of the alloy of RuO2 and Pt nanocrystals on intermediate adsorption during methanol oxidation. in Revue Roumaine de Chimie
Editura Academiei Romane., 65(5), 481-489.
https://doi.org/10.33224/rrch.2020.65.5.08
https://hdl.handle.net/21.15107/rcub_dais_10033
Spasojević M, Ribić Zelenović L, Spasojević M, Trišović T. The effect of the composition of the alloy of RuO2 and Pt nanocrystals on intermediate adsorption during methanol oxidation. in Revue Roumaine de Chimie. 2020;65(5):481-489.
doi:10.33224/rrch.2020.65.5.08
https://hdl.handle.net/21.15107/rcub_dais_10033 .
Spasojević, Milica, Ribić Zelenović, Lenka, Spasojević, Miroslav, Trišović, Tomislav, "The effect of the composition of the alloy of RuO2 and Pt nanocrystals on intermediate adsorption during methanol oxidation" in Revue Roumaine de Chimie, 65, no. 5 (2020):481-489,
https://doi.org/10.33224/rrch.2020.65.5.08 .,
https://hdl.handle.net/21.15107/rcub_dais_10033 .
5
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5

Morphological, microstructural and magnetic characteristics of electrodeposited Ni-Fe-W-Cu alloy powders

Spasojević, Miroslav; Ranđić, Siniša; Maričić, Aleksa; Trišović, Tomislav; Spasojević, Milica

(Springer, 2020)

TY  - JOUR
AU  - Spasojević, Miroslav
AU  - Ranđić, Siniša
AU  - Maričić, Aleksa
AU  - Trišović, Tomislav
AU  - Spasojević, Milica
PY  - 2020
UR  - https://dais.sanu.ac.rs/123456789/9451
AB  - Nanostructured Ni-Fe-W-Cu alloy powders were electrodeposited from an alkaline ammonium citrate solution on a titanium cathode. Powder particles were dendrite- and cauliflower-shaped. The dendritic particles had a high density of branches made up of interconnected globules. XRD analysis showed that the powder contained an amorphous matrix and FCC nanocrystals of the solid solution of Fe, W and Cu in Ni. As the deposition current density increased, the mean nanocrystal size decreased, and the mean value of internal microstrain and the total weight percent of Fe and Ni in the alloy increased. The powders deposited at higher current densities exhibited higher magnetization. During annealing at temperatures up to 460 °C, the powders underwent short-range ordering, which caused an increase in magnetization, whereas at temperatures above 460 °C, the magnetization decreased due to the formation of large FCC crystalline grains.
PB  - Springer
T2  - Science of Sintering
T1  - Morphological, microstructural and magnetic characteristics of electrodeposited Ni-Fe-W-Cu alloy powders
SP  - 109
EP  - 121
VL  - 52
IS  - 1
DO  - 10.2298/SOS2001109S
UR  - https://hdl.handle.net/21.15107/rcub_dais_9451
ER  - 
@article{
author = "Spasojević, Miroslav and Ranđić, Siniša and Maričić, Aleksa and Trišović, Tomislav and Spasojević, Milica",
year = "2020",
abstract = "Nanostructured Ni-Fe-W-Cu alloy powders were electrodeposited from an alkaline ammonium citrate solution on a titanium cathode. Powder particles were dendrite- and cauliflower-shaped. The dendritic particles had a high density of branches made up of interconnected globules. XRD analysis showed that the powder contained an amorphous matrix and FCC nanocrystals of the solid solution of Fe, W and Cu in Ni. As the deposition current density increased, the mean nanocrystal size decreased, and the mean value of internal microstrain and the total weight percent of Fe and Ni in the alloy increased. The powders deposited at higher current densities exhibited higher magnetization. During annealing at temperatures up to 460 °C, the powders underwent short-range ordering, which caused an increase in magnetization, whereas at temperatures above 460 °C, the magnetization decreased due to the formation of large FCC crystalline grains.",
publisher = "Springer",
journal = "Science of Sintering",
title = "Morphological, microstructural and magnetic characteristics of electrodeposited Ni-Fe-W-Cu alloy powders",
pages = "109-121",
volume = "52",
number = "1",
doi = "10.2298/SOS2001109S",
url = "https://hdl.handle.net/21.15107/rcub_dais_9451"
}
Spasojević, M., Ranđić, S., Maričić, A., Trišović, T.,& Spasojević, M.. (2020). Morphological, microstructural and magnetic characteristics of electrodeposited Ni-Fe-W-Cu alloy powders. in Science of Sintering
Springer., 52(1), 109-121.
https://doi.org/10.2298/SOS2001109S
https://hdl.handle.net/21.15107/rcub_dais_9451
Spasojević M, Ranđić S, Maričić A, Trišović T, Spasojević M. Morphological, microstructural and magnetic characteristics of electrodeposited Ni-Fe-W-Cu alloy powders. in Science of Sintering. 2020;52(1):109-121.
doi:10.2298/SOS2001109S
https://hdl.handle.net/21.15107/rcub_dais_9451 .
Spasojević, Miroslav, Ranđić, Siniša, Maričić, Aleksa, Trišović, Tomislav, Spasojević, Milica, "Morphological, microstructural and magnetic characteristics of electrodeposited Ni-Fe-W-Cu alloy powders" in Science of Sintering, 52, no. 1 (2020):109-121,
https://doi.org/10.2298/SOS2001109S .,
https://hdl.handle.net/21.15107/rcub_dais_9451 .
1
2
3

The Mixture of Nanoparticles of RuO2 and Pt Supported on Ti as an Efficient Catalyst for Direct Formic Acid Fuel Cell

Spasojević, Miroslav; Ribić Zelenović, Lenka; Spasojević, Milica; Trišović, Tomislav

(Springer, 2019)

TY  - JOUR
AU  - Spasojević, Miroslav
AU  - Ribić Zelenović, Lenka
AU  - Spasojević, Milica
AU  - Trišović, Tomislav
PY  - 2019
UR  - https://dais.sanu.ac.rs/123456789/8974
AB  - An active coating, composed of a mixture of nanocrystals of RuO2 with the rutile structure and nanocrystals of metal Pt, was thermally synthetized on a titanium substrate. Cyclic voltammograms and polarization curves showed that the catalytic activity of the coating for the formic acid oxidation in an acidic solution increased with an increase in the RuO2 content, reaching the maximum value at 50 mol % RuO2. Additionally, further increase in the RuO2 content resulted in a decline of the catalytic activity. The catalytic effect was attributed to a bifunctional mechanism and an electronic effect. The bifunctional mechanism had a dominant role and was based on the fact that Ru–OH species were formed on Ru atoms of RuO2 at more negative potentials than on Pt. Those species oxidized the adsorbed COad and HCOOad—species on adjacent Pt atoms of clusters of metal Pt and thus discharge them to oxidize new HCOOH molecules.
PB  - Springer
T2  - Russian Journal of Electrochemistry
T1  - The Mixture of Nanoparticles of RuO2 and Pt Supported on Ti as an Efficient Catalyst for Direct Formic Acid Fuel Cell
SP  - 1350
EP  - 1359
VL  - 55
IS  - 12
DO  - 10.1134/S1023193519120164
UR  - https://hdl.handle.net/21.15107/rcub_dais_8974
ER  - 
@article{
author = "Spasojević, Miroslav and Ribić Zelenović, Lenka and Spasojević, Milica and Trišović, Tomislav",
year = "2019",
abstract = "An active coating, composed of a mixture of nanocrystals of RuO2 with the rutile structure and nanocrystals of metal Pt, was thermally synthetized on a titanium substrate. Cyclic voltammograms and polarization curves showed that the catalytic activity of the coating for the formic acid oxidation in an acidic solution increased with an increase in the RuO2 content, reaching the maximum value at 50 mol % RuO2. Additionally, further increase in the RuO2 content resulted in a decline of the catalytic activity. The catalytic effect was attributed to a bifunctional mechanism and an electronic effect. The bifunctional mechanism had a dominant role and was based on the fact that Ru–OH species were formed on Ru atoms of RuO2 at more negative potentials than on Pt. Those species oxidized the adsorbed COad and HCOOad—species on adjacent Pt atoms of clusters of metal Pt and thus discharge them to oxidize new HCOOH molecules.",
publisher = "Springer",
journal = "Russian Journal of Electrochemistry",
title = "The Mixture of Nanoparticles of RuO2 and Pt Supported on Ti as an Efficient Catalyst for Direct Formic Acid Fuel Cell",
pages = "1350-1359",
volume = "55",
number = "12",
doi = "10.1134/S1023193519120164",
url = "https://hdl.handle.net/21.15107/rcub_dais_8974"
}
Spasojević, M., Ribić Zelenović, L., Spasojević, M.,& Trišović, T.. (2019). The Mixture of Nanoparticles of RuO2 and Pt Supported on Ti as an Efficient Catalyst for Direct Formic Acid Fuel Cell. in Russian Journal of Electrochemistry
Springer., 55(12), 1350-1359.
https://doi.org/10.1134/S1023193519120164
https://hdl.handle.net/21.15107/rcub_dais_8974
Spasojević M, Ribić Zelenović L, Spasojević M, Trišović T. The Mixture of Nanoparticles of RuO2 and Pt Supported on Ti as an Efficient Catalyst for Direct Formic Acid Fuel Cell. in Russian Journal of Electrochemistry. 2019;55(12):1350-1359.
doi:10.1134/S1023193519120164
https://hdl.handle.net/21.15107/rcub_dais_8974 .
Spasojević, Miroslav, Ribić Zelenović, Lenka, Spasojević, Milica, Trišović, Tomislav, "The Mixture of Nanoparticles of RuO2 and Pt Supported on Ti as an Efficient Catalyst for Direct Formic Acid Fuel Cell" in Russian Journal of Electrochemistry, 55, no. 12 (2019):1350-1359,
https://doi.org/10.1134/S1023193519120164 .,
https://hdl.handle.net/21.15107/rcub_dais_8974 .
7
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The Mixture of Nanoparticles of RuO2 and Pt Supported on Ti as an Efficient Catalyst for Direct Formic Acid Fuel Cell

Spasojević, Miroslav; Ribić Zelenović, Lenka; Spasojević, Milica; Trišović, Tomislav

(Springer, 2019)

TY  - JOUR
AU  - Spasojević, Miroslav
AU  - Ribić Zelenović, Lenka
AU  - Spasojević, Milica
AU  - Trišović, Tomislav
PY  - 2019
UR  - https://dais.sanu.ac.rs/123456789/8973
AB  - An active coating, composed of a mixture of nanocrystals of RuO2 with the rutile structure and nanocrystals of metal Pt, was thermally synthetized on a titanium substrate. Cyclic voltammograms and polarization curves showed that the catalytic activity of the coating for the formic acid oxidation in an acidic solution increased with an increase in the RuO2 content, reaching the maximum value at 50 mol % RuO2. Additionally, further increase in the RuO2 content resulted in a decline of the catalytic activity. The catalytic effect was attributed to a bifunctional mechanism and an electronic effect. The bifunctional mechanism had a dominant role and was based on the fact that Ru–OH species were formed on Ru atoms of RuO2 at more negative potentials than on Pt. Those species oxidized the adsorbed COad and HCOOad—species on adjacent Pt atoms of clusters of metal Pt and thus discharge them to oxidize new HCOOH molecules.
PB  - Springer
T2  - Russian Journal of Electrochemistry
T1  - The Mixture of Nanoparticles of RuO2 and Pt Supported on Ti as an Efficient Catalyst for Direct Formic Acid Fuel Cell
SP  - 1350
EP  - 1359
VL  - 55
IS  - 12
DO  - 10.1134/S1023193519120164
UR  - https://hdl.handle.net/21.15107/rcub_dais_8973
ER  - 
@article{
author = "Spasojević, Miroslav and Ribić Zelenović, Lenka and Spasojević, Milica and Trišović, Tomislav",
year = "2019",
abstract = "An active coating, composed of a mixture of nanocrystals of RuO2 with the rutile structure and nanocrystals of metal Pt, was thermally synthetized on a titanium substrate. Cyclic voltammograms and polarization curves showed that the catalytic activity of the coating for the formic acid oxidation in an acidic solution increased with an increase in the RuO2 content, reaching the maximum value at 50 mol % RuO2. Additionally, further increase in the RuO2 content resulted in a decline of the catalytic activity. The catalytic effect was attributed to a bifunctional mechanism and an electronic effect. The bifunctional mechanism had a dominant role and was based on the fact that Ru–OH species were formed on Ru atoms of RuO2 at more negative potentials than on Pt. Those species oxidized the adsorbed COad and HCOOad—species on adjacent Pt atoms of clusters of metal Pt and thus discharge them to oxidize new HCOOH molecules.",
publisher = "Springer",
journal = "Russian Journal of Electrochemistry",
title = "The Mixture of Nanoparticles of RuO2 and Pt Supported on Ti as an Efficient Catalyst for Direct Formic Acid Fuel Cell",
pages = "1350-1359",
volume = "55",
number = "12",
doi = "10.1134/S1023193519120164",
url = "https://hdl.handle.net/21.15107/rcub_dais_8973"
}
Spasojević, M., Ribić Zelenović, L., Spasojević, M.,& Trišović, T.. (2019). The Mixture of Nanoparticles of RuO2 and Pt Supported on Ti as an Efficient Catalyst for Direct Formic Acid Fuel Cell. in Russian Journal of Electrochemistry
Springer., 55(12), 1350-1359.
https://doi.org/10.1134/S1023193519120164
https://hdl.handle.net/21.15107/rcub_dais_8973
Spasojević M, Ribić Zelenović L, Spasojević M, Trišović T. The Mixture of Nanoparticles of RuO2 and Pt Supported on Ti as an Efficient Catalyst for Direct Formic Acid Fuel Cell. in Russian Journal of Electrochemistry. 2019;55(12):1350-1359.
doi:10.1134/S1023193519120164
https://hdl.handle.net/21.15107/rcub_dais_8973 .
Spasojević, Miroslav, Ribić Zelenović, Lenka, Spasojević, Milica, Trišović, Tomislav, "The Mixture of Nanoparticles of RuO2 and Pt Supported on Ti as an Efficient Catalyst for Direct Formic Acid Fuel Cell" in Russian Journal of Electrochemistry, 55, no. 12 (2019):1350-1359,
https://doi.org/10.1134/S1023193519120164 .,
https://hdl.handle.net/21.15107/rcub_dais_8973 .
7
4
7

Mathematical model of the catalytic effect of chromium(VI) on hypochlorite disproportionation in chlorate electrolysis

Spasojević, Miroslav; Marković, D.; Trišović, Tomislav; Spasojević, Milica

(Pennington N.J. : Electrochemical Society, 2018)

TY  - JOUR
AU  - Spasojević, Miroslav
AU  - Marković, D.
AU  - Trišović, Tomislav
AU  - Spasojević, Milica
PY  - 2018
UR  - https://dais.sanu.ac.rs/123456789/8970
AB  - The effect of chromium(VI) on the kinetics of disproportionation of hypochlorous acid and hypochlorite was established in the solution for the electrolytic production of chlorate. The hexavalent chromium species Cr2O7 2-, HCrO4 - and CrO4 2- present in the solution catalyze the disproportionation reaction. In both the absence and presence of chromium(VI), disproportionation is a third-order reaction with respect to HClO and ClO-P, and a first-order reaction with respect to the hexavalent chromium species. In the presence of chromium(VI) ions, four parallel reactions probably take place in the solution i.e. uncatalyzed disproportionation and three parallel reactions catalyzed by Cr2O7 2-, HCrO4 - and CrO4 2-ions. Most likely, the hexavalent chromium species do not change the sequence of elementary reactions in the disproportionation mechanism but only speed up the rate-determining step through interaction with its reactants. In the chlorate production process, as chromium(VI) concentration increases, the optimum pH which ensures the maximum rate of disproportionation is shifted to an acid environment. This is due to an increase in the concentration of the catalytically most active species HCrO4 - with increasing acidity of the solution. A mathematical model of the kinetics of the chromium(VI)-catalyzed disproportionation of hypochlorite and hypochlorous acid into chlorate was set up. Good agreement was obtained between theoretical and experimental data. © 2018 The Electrochemical Society.
PB  - Pennington N.J. : Electrochemical Society
T2  - Journal of the Electrochemical Society
T1  - Mathematical model of the catalytic effect of chromium(VI) on hypochlorite disproportionation in chlorate electrolysis
SP  - E8
EP  - E19
VL  - 165
IS  - 2
DO  - 10.1149/2.0291802jes
UR  - https://hdl.handle.net/21.15107/rcub_dais_8970
ER  - 
@article{
author = "Spasojević, Miroslav and Marković, D. and Trišović, Tomislav and Spasojević, Milica",
year = "2018",
abstract = "The effect of chromium(VI) on the kinetics of disproportionation of hypochlorous acid and hypochlorite was established in the solution for the electrolytic production of chlorate. The hexavalent chromium species Cr2O7 2-, HCrO4 - and CrO4 2- present in the solution catalyze the disproportionation reaction. In both the absence and presence of chromium(VI), disproportionation is a third-order reaction with respect to HClO and ClO-P, and a first-order reaction with respect to the hexavalent chromium species. In the presence of chromium(VI) ions, four parallel reactions probably take place in the solution i.e. uncatalyzed disproportionation and three parallel reactions catalyzed by Cr2O7 2-, HCrO4 - and CrO4 2-ions. Most likely, the hexavalent chromium species do not change the sequence of elementary reactions in the disproportionation mechanism but only speed up the rate-determining step through interaction with its reactants. In the chlorate production process, as chromium(VI) concentration increases, the optimum pH which ensures the maximum rate of disproportionation is shifted to an acid environment. This is due to an increase in the concentration of the catalytically most active species HCrO4 - with increasing acidity of the solution. A mathematical model of the kinetics of the chromium(VI)-catalyzed disproportionation of hypochlorite and hypochlorous acid into chlorate was set up. Good agreement was obtained between theoretical and experimental data. © 2018 The Electrochemical Society.",
publisher = "Pennington N.J. : Electrochemical Society",
journal = "Journal of the Electrochemical Society",
title = "Mathematical model of the catalytic effect of chromium(VI) on hypochlorite disproportionation in chlorate electrolysis",
pages = "E8-E19",
volume = "165",
number = "2",
doi = "10.1149/2.0291802jes",
url = "https://hdl.handle.net/21.15107/rcub_dais_8970"
}
Spasojević, M., Marković, D., Trišović, T.,& Spasojević, M.. (2018). Mathematical model of the catalytic effect of chromium(VI) on hypochlorite disproportionation in chlorate electrolysis. in Journal of the Electrochemical Society
Pennington N.J. : Electrochemical Society., 165(2), E8-E19.
https://doi.org/10.1149/2.0291802jes
https://hdl.handle.net/21.15107/rcub_dais_8970
Spasojević M, Marković D, Trišović T, Spasojević M. Mathematical model of the catalytic effect of chromium(VI) on hypochlorite disproportionation in chlorate electrolysis. in Journal of the Electrochemical Society. 2018;165(2):E8-E19.
doi:10.1149/2.0291802jes
https://hdl.handle.net/21.15107/rcub_dais_8970 .
Spasojević, Miroslav, Marković, D., Trišović, Tomislav, Spasojević, Milica, "Mathematical model of the catalytic effect of chromium(VI) on hypochlorite disproportionation in chlorate electrolysis" in Journal of the Electrochemical Society, 165, no. 2 (2018):E8-E19,
https://doi.org/10.1149/2.0291802jes .,
https://hdl.handle.net/21.15107/rcub_dais_8970 .
12
8
12

Mathematical model of the catalytic effect of chromium(VI) on hypochlorite disproportionation in chlorate electrolysis

Spasojević, Miroslav; Marković, D.; Trišović, Tomislav; Spasojević, Milica

(Pennington N.J. : Electrochemical Society, 2018)

TY  - JOUR
AU  - Spasojević, Miroslav
AU  - Marković, D.
AU  - Trišović, Tomislav
AU  - Spasojević, Milica
PY  - 2018
UR  - https://dais.sanu.ac.rs/123456789/3750
AB  - The effect of chromium(VI) on the kinetics of disproportionation of hypochlorous acid and hypochlorite was established in the solution for the electrolytic production of chlorate. The hexavalent chromium species Cr2O7 2-, HCrO4 - and CrO4 2- present in the solution catalyze the disproportionation reaction. In both the absence and presence of chromium(VI), disproportionation is a third-order reaction with respect to HClO and ClO-P, and a first-order reaction with respect to the hexavalent chromium species. In the presence of chromium(VI) ions, four parallel reactions probably take place in the solution i.e. uncatalyzed disproportionation and three parallel reactions catalyzed by Cr2O7 2-, HCrO4 - and CrO4 2-ions. Most likely, the hexavalent chromium species do not change the sequence of elementary reactions in the disproportionation mechanism but only speed up the rate-determining step through interaction with its reactants. In the chlorate production process, as chromium(VI) concentration increases, the optimum pH which ensures the maximum rate of disproportionation is shifted to an acid environment. This is due to an increase in the concentration of the catalytically most active species HCrO4 - with increasing acidity of the solution. A mathematical model of the kinetics of the chromium(VI)-catalyzed disproportionation of hypochlorite and hypochlorous acid into chlorate was set up. Good agreement was obtained between theoretical and experimental data. © 2018 The Electrochemical Society.
PB  - Pennington N.J. : Electrochemical Society
T2  - Journal of the Electrochemical Society
T1  - Mathematical model of the catalytic effect of chromium(VI) on hypochlorite disproportionation in chlorate electrolysis
SP  - E8
EP  - E19
VL  - 165
IS  - 2
DO  - 10.1149/2.0291802jes
UR  - https://hdl.handle.net/21.15107/rcub_dais_3750
ER  - 
@article{
author = "Spasojević, Miroslav and Marković, D. and Trišović, Tomislav and Spasojević, Milica",
year = "2018",
abstract = "The effect of chromium(VI) on the kinetics of disproportionation of hypochlorous acid and hypochlorite was established in the solution for the electrolytic production of chlorate. The hexavalent chromium species Cr2O7 2-, HCrO4 - and CrO4 2- present in the solution catalyze the disproportionation reaction. In both the absence and presence of chromium(VI), disproportionation is a third-order reaction with respect to HClO and ClO-P, and a first-order reaction with respect to the hexavalent chromium species. In the presence of chromium(VI) ions, four parallel reactions probably take place in the solution i.e. uncatalyzed disproportionation and three parallel reactions catalyzed by Cr2O7 2-, HCrO4 - and CrO4 2-ions. Most likely, the hexavalent chromium species do not change the sequence of elementary reactions in the disproportionation mechanism but only speed up the rate-determining step through interaction with its reactants. In the chlorate production process, as chromium(VI) concentration increases, the optimum pH which ensures the maximum rate of disproportionation is shifted to an acid environment. This is due to an increase in the concentration of the catalytically most active species HCrO4 - with increasing acidity of the solution. A mathematical model of the kinetics of the chromium(VI)-catalyzed disproportionation of hypochlorite and hypochlorous acid into chlorate was set up. Good agreement was obtained between theoretical and experimental data. © 2018 The Electrochemical Society.",
publisher = "Pennington N.J. : Electrochemical Society",
journal = "Journal of the Electrochemical Society",
title = "Mathematical model of the catalytic effect of chromium(VI) on hypochlorite disproportionation in chlorate electrolysis",
pages = "E8-E19",
volume = "165",
number = "2",
doi = "10.1149/2.0291802jes",
url = "https://hdl.handle.net/21.15107/rcub_dais_3750"
}
Spasojević, M., Marković, D., Trišović, T.,& Spasojević, M.. (2018). Mathematical model of the catalytic effect of chromium(VI) on hypochlorite disproportionation in chlorate electrolysis. in Journal of the Electrochemical Society
Pennington N.J. : Electrochemical Society., 165(2), E8-E19.
https://doi.org/10.1149/2.0291802jes
https://hdl.handle.net/21.15107/rcub_dais_3750
Spasojević M, Marković D, Trišović T, Spasojević M. Mathematical model of the catalytic effect of chromium(VI) on hypochlorite disproportionation in chlorate electrolysis. in Journal of the Electrochemical Society. 2018;165(2):E8-E19.
doi:10.1149/2.0291802jes
https://hdl.handle.net/21.15107/rcub_dais_3750 .
Spasojević, Miroslav, Marković, D., Trišović, Tomislav, Spasojević, Milica, "Mathematical model of the catalytic effect of chromium(VI) on hypochlorite disproportionation in chlorate electrolysis" in Journal of the Electrochemical Society, 165, no. 2 (2018):E8-E19,
https://doi.org/10.1149/2.0291802jes .,
https://hdl.handle.net/21.15107/rcub_dais_3750 .
12
8
12

Morphological, microstructural and magnetic characteristics of electrodeposited Ni-Fe-W-Cu alloy powders

Trišović, Tomislav; Spasojević, Miroslav; Maričić, Aleksa; Spasojević, Milica

(Belgrade : Materials Research Society of Serbia, 2018)

TY  - CONF
AU  - Trišović, Tomislav
AU  - Spasojević, Miroslav
AU  - Maričić, Aleksa
AU  - Spasojević, Milica
PY  - 2018
UR  - https://dais.sanu.ac.rs/123456789/3661
AB  - Nanostructured Ni-Fe-W-Cu alloy powders were electrodeposited from an alkaline ammonium citrate solution on a titanium cathode. Powder particles were dendrite- and cauliflower-shaped. The dendritic particles had a high density of branches made up of interconnected globules. XRD analysis showed that the powder contained an amorphous matrix and FCC nanocrystals of the solid solution of Fe, W and Cu in Ni. As the deposition current density increased, the mean nanocrystal size decreased, and the mean value of internal microstrain and the total weight percent of Fe and Ni in the alloy increased. The powders deposited at higher current densities exhibited higher magnetization. During annealing at temperatures up to 460°C, the powders underwent short-range ordering, which caused an increase in magnetization, whereas at temperatures above 460°C, the magnetization decreased due to the formation of large FCC crystalline grains.
PB  - Belgrade : Materials Research Society of Serbia
C3  - Programme and The Book of Abstracts / Twentieth Annual Conference YUCOMAT 2018, Herceg Novi, September 3-7, 2018
T1  - Morphological, microstructural and magnetic characteristics of electrodeposited Ni-Fe-W-Cu alloy powders
SP  - 120
EP  - 120
UR  - https://hdl.handle.net/21.15107/rcub_dais_3661
ER  - 
@conference{
author = "Trišović, Tomislav and Spasojević, Miroslav and Maričić, Aleksa and Spasojević, Milica",
year = "2018",
abstract = "Nanostructured Ni-Fe-W-Cu alloy powders were electrodeposited from an alkaline ammonium citrate solution on a titanium cathode. Powder particles were dendrite- and cauliflower-shaped. The dendritic particles had a high density of branches made up of interconnected globules. XRD analysis showed that the powder contained an amorphous matrix and FCC nanocrystals of the solid solution of Fe, W and Cu in Ni. As the deposition current density increased, the mean nanocrystal size decreased, and the mean value of internal microstrain and the total weight percent of Fe and Ni in the alloy increased. The powders deposited at higher current densities exhibited higher magnetization. During annealing at temperatures up to 460°C, the powders underwent short-range ordering, which caused an increase in magnetization, whereas at temperatures above 460°C, the magnetization decreased due to the formation of large FCC crystalline grains.",
publisher = "Belgrade : Materials Research Society of Serbia",
journal = "Programme and The Book of Abstracts / Twentieth Annual Conference YUCOMAT 2018, Herceg Novi, September 3-7, 2018",
title = "Morphological, microstructural and magnetic characteristics of electrodeposited Ni-Fe-W-Cu alloy powders",
pages = "120-120",
url = "https://hdl.handle.net/21.15107/rcub_dais_3661"
}
Trišović, T., Spasojević, M., Maričić, A.,& Spasojević, M.. (2018). Morphological, microstructural and magnetic characteristics of electrodeposited Ni-Fe-W-Cu alloy powders. in Programme and The Book of Abstracts / Twentieth Annual Conference YUCOMAT 2018, Herceg Novi, September 3-7, 2018
Belgrade : Materials Research Society of Serbia., 120-120.
https://hdl.handle.net/21.15107/rcub_dais_3661
Trišović T, Spasojević M, Maričić A, Spasojević M. Morphological, microstructural and magnetic characteristics of electrodeposited Ni-Fe-W-Cu alloy powders. in Programme and The Book of Abstracts / Twentieth Annual Conference YUCOMAT 2018, Herceg Novi, September 3-7, 2018. 2018;:120-120.
https://hdl.handle.net/21.15107/rcub_dais_3661 .
Trišović, Tomislav, Spasojević, Miroslav, Maričić, Aleksa, Spasojević, Milica, "Morphological, microstructural and magnetic characteristics of electrodeposited Ni-Fe-W-Cu alloy powders" in Programme and The Book of Abstracts / Twentieth Annual Conference YUCOMAT 2018, Herceg Novi, September 3-7, 2018 (2018):120-120,
https://hdl.handle.net/21.15107/rcub_dais_3661 .

Development of RuO2/TiO2 titanium anodes and a device for in situ active chlorine generation

Spasojević, Miroslav; Trišović, Tomislav; Ribić-Zelenović, Lenka; Spasojević, Pavle

(Belgrade : Association of the Chemical Engineers of Serbia, 2013)

TY  - JOUR
AU  - Spasojević, Miroslav
AU  - Trišović, Tomislav
AU  - Ribić-Zelenović, Lenka
AU  - Spasojević, Pavle
PY  - 2013
UR  - https://dais.sanu.ac.rs/123456789/379
AB  - Chlorine is used worldwide for water disinfection purposes. However, due to its toxicity the EU has imposed a set of standards that must be applied when transporting and storing chlorine. In Serbia, numerous studies have been conducted attempting to develop the technology for the generation of active chlorine disinfectant but with a non-toxic aqueous solution of sodium chloride as the raw material. This study provides an overview of the titanium anodes activated by thermally obtained solid solution of ruthenium and titanium oxide development. It also presents new findings on the effect of the temperature of thermal treatment, the composition, the thickness of an active coating on its microstructural properties, and consequently on the catalytic activity, ion selectivity, and corrosion stability during active chlorine generation through the electrolysis of dilute sodium chloride solutions at room temperature. The study also evaluates the effect of the kinetic and operational parameters of the electrochemical process of active chlorine generation on both current and energy efficiencies. The results obtained were used to determine optimal values of technological parameters of the production process. This comprehensive research resulted in the construction of different types of remote-controlled and fully automated active chlorine generating plants.
AB  - U radu je dat pregled razvoja aktivnih titanskih anoda za reakciju oksidacije hloridnih jona u istraživačkim laboratorijama u Srbiji. Prikazani su i novi rezultati istraživanja efekta temperature termičke obrade, sastava i debljine aktivne RuO2/TiO2 prevlake na titanu na njena mikrostrukturna svojstva i odraz ovih svojstava na katalitičku aktivnost, jonselektivnost i korozionu stabilnost u procesu dobijanja aktivnog hlora. Ustanovljen je i efekat kinetičkih i operativnih parametara procesa elektrolize razblaženih rastvora natrijum-hlorida na iskorišćenje struje i energije po aktivnom hloru. Na osnovu ovih ispitivanja konstruisana je ćelija za elektrolizu i utvrđene su optimalne vrednosti tehnoloških parametara procesa proizvodnje aktivnog hlora. Sveobuhvatna istraživanja rezultirala su konstrukcijom različitih tipova postrojenja za in situ proizvodnju aktivnog hlora.
PB  - Belgrade : Association of the Chemical Engineers of Serbia
T2  - Hemijska industrija
T1  - Development of RuO2/TiO2 titanium anodes and a device for in situ active chlorine generation
SP  - 313
EP  - 321
VL  - 67
IS  - 2
DO  - 10.2298/HEMIND120414076S
UR  - https://hdl.handle.net/21.15107/rcub_dais_379
ER  - 
@article{
author = "Spasojević, Miroslav and Trišović, Tomislav and Ribić-Zelenović, Lenka and Spasojević, Pavle",
year = "2013",
abstract = "Chlorine is used worldwide for water disinfection purposes. However, due to its toxicity the EU has imposed a set of standards that must be applied when transporting and storing chlorine. In Serbia, numerous studies have been conducted attempting to develop the technology for the generation of active chlorine disinfectant but with a non-toxic aqueous solution of sodium chloride as the raw material. This study provides an overview of the titanium anodes activated by thermally obtained solid solution of ruthenium and titanium oxide development. It also presents new findings on the effect of the temperature of thermal treatment, the composition, the thickness of an active coating on its microstructural properties, and consequently on the catalytic activity, ion selectivity, and corrosion stability during active chlorine generation through the electrolysis of dilute sodium chloride solutions at room temperature. The study also evaluates the effect of the kinetic and operational parameters of the electrochemical process of active chlorine generation on both current and energy efficiencies. The results obtained were used to determine optimal values of technological parameters of the production process. This comprehensive research resulted in the construction of different types of remote-controlled and fully automated active chlorine generating plants., U radu je dat pregled razvoja aktivnih titanskih anoda za reakciju oksidacije hloridnih jona u istraživačkim laboratorijama u Srbiji. Prikazani su i novi rezultati istraživanja efekta temperature termičke obrade, sastava i debljine aktivne RuO2/TiO2 prevlake na titanu na njena mikrostrukturna svojstva i odraz ovih svojstava na katalitičku aktivnost, jonselektivnost i korozionu stabilnost u procesu dobijanja aktivnog hlora. Ustanovljen je i efekat kinetičkih i operativnih parametara procesa elektrolize razblaženih rastvora natrijum-hlorida na iskorišćenje struje i energije po aktivnom hloru. Na osnovu ovih ispitivanja konstruisana je ćelija za elektrolizu i utvrđene su optimalne vrednosti tehnoloških parametara procesa proizvodnje aktivnog hlora. Sveobuhvatna istraživanja rezultirala su konstrukcijom različitih tipova postrojenja za in situ proizvodnju aktivnog hlora.",
publisher = "Belgrade : Association of the Chemical Engineers of Serbia",
journal = "Hemijska industrija",
title = "Development of RuO2/TiO2 titanium anodes and a device for in situ active chlorine generation",
pages = "313-321",
volume = "67",
number = "2",
doi = "10.2298/HEMIND120414076S",
url = "https://hdl.handle.net/21.15107/rcub_dais_379"
}
Spasojević, M., Trišović, T., Ribić-Zelenović, L.,& Spasojević, P.. (2013). Development of RuO2/TiO2 titanium anodes and a device for in situ active chlorine generation. in Hemijska industrija
Belgrade : Association of the Chemical Engineers of Serbia., 67(2), 313-321.
https://doi.org/10.2298/HEMIND120414076S
https://hdl.handle.net/21.15107/rcub_dais_379
Spasojević M, Trišović T, Ribić-Zelenović L, Spasojević P. Development of RuO2/TiO2 titanium anodes and a device for in situ active chlorine generation. in Hemijska industrija. 2013;67(2):313-321.
doi:10.2298/HEMIND120414076S
https://hdl.handle.net/21.15107/rcub_dais_379 .
Spasojević, Miroslav, Trišović, Tomislav, Ribić-Zelenović, Lenka, Spasojević, Pavle, "Development of RuO2/TiO2 titanium anodes and a device for in situ active chlorine generation" in Hemijska industrija, 67, no. 2 (2013):313-321,
https://doi.org/10.2298/HEMIND120414076S .,
https://hdl.handle.net/21.15107/rcub_dais_379 .
4
4
5

The kinetics of the electrochemical reduction of xylose on amalgamated zinc

Spasojević, Miroslav; Ribić Zelenović, Lenka; Trišović, Tomislav

(Čačak : University of Kragujevac - Faculty of Agronomy, 2009)

TY  - JOUR
AU  - Spasojević, Miroslav
AU  - Ribić Zelenović, Lenka
AU  - Trišović, Tomislav
PY  - 2009
UR  - https://dais.sanu.ac.rs/123456789/14863
AB  - During the electrolysis of an aqueous solution of xylose, two parallel reactions take place on the cathode i.e. the reduction of xylose to xylitol and hydrogen evolution. To favor the desired reaction of xylose reduction, amalgamated zinc is used to perform the reduction in this study. The catalytic amalgamated coating is formed by the electrodeposition of a zinc coating having desired properties on a copper mesh from a sulfate bath and its subsequent immersion into the HgCl2 solution to obtain the amalgamated zinc of adequate concentration. The present study focuses on the kinetics and mechanism of two parallel reactions of hydrogen evolution and xylose reduction on amalgamated zinc from a solution containing xylose and Na2SO4 as a basic electrolyte. The hydrogen evolution reaction occurs through two parallel mechanisms, either in the presence or absence of xylose. At lower overpotentials, hydrogen is evolved on zinc oxide in three consecutive elementary steps. The overall rate of the hydrogen evolution reaction within the limiting current range is governed by the heterogeneous chemical step involving a Zn-H species. At potentials more negative than -2.0 V, the reaction takes place on the metal surface through the Volmer-Heyrovsky mechanism. Xylose is adsorbed on the metallic zinc. At potentials more negative than -1.25 V, the adsorbed xylose molecules are reduced with Zn-H to xylitol. The cathodic polarization curves, in either the presence or absence of xylose, were used to determine the cathodic current efficiency for xylitol production, which is in good agreement with the values obtained by other methods.
AB  - Tokom elektrolize vodenog rastvora ksiloze na katodi se paralelno odigravaju dve reakcije: redukcija ksiloze do ksilitola i reakcija izdvajanja vodonika. Da bi se favorizovala željena reakcija redukcije ksiloze u ovom radu je redukcija izvođena na amalgamu cinka. Katalitička prevlaka amalgama formirana je na taj način što je izborom parametara elektrolize iz sulfatnog kupatila na bakarnoj mreži najpre istaložena prevlaka cinka željenih karakteristika, a zatim zamakanjem prevlake u rastvor HgCl2 dobijen amalgam cinka odgovarajuće koncentracije. Ispitivana je kinetika i mehanizam paralelnih reakcija izdvajanja vodonika i redukcije ksiloze na amalgamu cinka iz rastvora koji sadrži ksilozu i Na2SO4 kao osnovni elektrolit. Reakcija izdvajanja vodonika se odigrava preko dva paralelna mehanizma, i u prisustvu i u odsustvu ksiloze u rastvoru. Na nižim prenapetostima reakcija izdvajanja vodonika se odvija na oksidu cinka sa tri konsekutivna elementarna stupnja. Heterogeni hemijski stupanj u kome učestvuje čestica Zn-H kontroliše ukupnu brzinu reakcije u oblasti granične struje. Na potencijalima negativnijim od -2,0 V reakcija izdvajanja vodonika se dominantno odigrava na metalnoj površini Folmer-Heirovskim reakcionim mehanizmom. Ksiloza se adsorbuje na metalnom cinku. Na potencijalima negativnijim od -1,25 V adsorbovani molekuli ksiloze se reduju sa Zn-H do ksilitola. Na osnovu katodnih polarizacionih krivih u odsustvu i u prisustvu ksiloze određeno je katodno iskorišćenje struje po ksilitolu.
PB  - Čačak : University of Kragujevac - Faculty of Agronomy
T2  - Acta agriculturae Serbica
T1  - The kinetics of the electrochemical reduction of xylose on amalgamated zinc
T1  - Kinetika elektrohemijske redukcije ksiloze na amalgamu cinka
EP  - 11
VL  - 14
IS  - 28
UR  - https://hdl.handle.net/21.15107/rcub_dais_14863
ER  - 
@article{
author = "Spasojević, Miroslav and Ribić Zelenović, Lenka and Trišović, Tomislav",
year = "2009",
abstract = "During the electrolysis of an aqueous solution of xylose, two parallel reactions take place on the cathode i.e. the reduction of xylose to xylitol and hydrogen evolution. To favor the desired reaction of xylose reduction, amalgamated zinc is used to perform the reduction in this study. The catalytic amalgamated coating is formed by the electrodeposition of a zinc coating having desired properties on a copper mesh from a sulfate bath and its subsequent immersion into the HgCl2 solution to obtain the amalgamated zinc of adequate concentration. The present study focuses on the kinetics and mechanism of two parallel reactions of hydrogen evolution and xylose reduction on amalgamated zinc from a solution containing xylose and Na2SO4 as a basic electrolyte. The hydrogen evolution reaction occurs through two parallel mechanisms, either in the presence or absence of xylose. At lower overpotentials, hydrogen is evolved on zinc oxide in three consecutive elementary steps. The overall rate of the hydrogen evolution reaction within the limiting current range is governed by the heterogeneous chemical step involving a Zn-H species. At potentials more negative than -2.0 V, the reaction takes place on the metal surface through the Volmer-Heyrovsky mechanism. Xylose is adsorbed on the metallic zinc. At potentials more negative than -1.25 V, the adsorbed xylose molecules are reduced with Zn-H to xylitol. The cathodic polarization curves, in either the presence or absence of xylose, were used to determine the cathodic current efficiency for xylitol production, which is in good agreement with the values obtained by other methods., Tokom elektrolize vodenog rastvora ksiloze na katodi se paralelno odigravaju dve reakcije: redukcija ksiloze do ksilitola i reakcija izdvajanja vodonika. Da bi se favorizovala željena reakcija redukcije ksiloze u ovom radu je redukcija izvođena na amalgamu cinka. Katalitička prevlaka amalgama formirana je na taj način što je izborom parametara elektrolize iz sulfatnog kupatila na bakarnoj mreži najpre istaložena prevlaka cinka željenih karakteristika, a zatim zamakanjem prevlake u rastvor HgCl2 dobijen amalgam cinka odgovarajuće koncentracije. Ispitivana je kinetika i mehanizam paralelnih reakcija izdvajanja vodonika i redukcije ksiloze na amalgamu cinka iz rastvora koji sadrži ksilozu i Na2SO4 kao osnovni elektrolit. Reakcija izdvajanja vodonika se odigrava preko dva paralelna mehanizma, i u prisustvu i u odsustvu ksiloze u rastvoru. Na nižim prenapetostima reakcija izdvajanja vodonika se odvija na oksidu cinka sa tri konsekutivna elementarna stupnja. Heterogeni hemijski stupanj u kome učestvuje čestica Zn-H kontroliše ukupnu brzinu reakcije u oblasti granične struje. Na potencijalima negativnijim od -2,0 V reakcija izdvajanja vodonika se dominantno odigrava na metalnoj površini Folmer-Heirovskim reakcionim mehanizmom. Ksiloza se adsorbuje na metalnom cinku. Na potencijalima negativnijim od -1,25 V adsorbovani molekuli ksiloze se reduju sa Zn-H do ksilitola. Na osnovu katodnih polarizacionih krivih u odsustvu i u prisustvu ksiloze određeno je katodno iskorišćenje struje po ksilitolu.",
publisher = "Čačak : University of Kragujevac - Faculty of Agronomy",
journal = "Acta agriculturae Serbica",
title = "The kinetics of the electrochemical reduction of xylose on amalgamated zinc, Kinetika elektrohemijske redukcije ksiloze na amalgamu cinka",
pages = "11",
volume = "14",
number = "28",
url = "https://hdl.handle.net/21.15107/rcub_dais_14863"
}
Spasojević, M., Ribić Zelenović, L.,& Trišović, T.. (2009). The kinetics of the electrochemical reduction of xylose on amalgamated zinc. in Acta agriculturae Serbica
Čačak : University of Kragujevac - Faculty of Agronomy., 14(28).
https://hdl.handle.net/21.15107/rcub_dais_14863
Spasojević M, Ribić Zelenović L, Trišović T. The kinetics of the electrochemical reduction of xylose on amalgamated zinc. in Acta agriculturae Serbica. 2009;14(28):null-11.
https://hdl.handle.net/21.15107/rcub_dais_14863 .
Spasojević, Miroslav, Ribić Zelenović, Lenka, Trišović, Tomislav, "The kinetics of the electrochemical reduction of xylose on amalgamated zinc" in Acta agriculturae Serbica, 14, no. 28 (2009),
https://hdl.handle.net/21.15107/rcub_dais_14863 .