Milanović, Igor

Link to this page

Authority KeyName Variants
orcid::0000-0003-0174-9139
  • Milanović, Igor (19)
Projects
Synthesis, processing and characterization of nanostructured materials for application in the field of energy, mechanical engineering, environmental protection and biomedicine Ministry of Education, Science and Technological Development of the Republic of Serbia
Serbia-Slovenia bilateral research project [BIRS/16/17051] Slovenian Research Agency [P10125]
Acciones Integradas program of Spanish MICINN [IB2010SE-00191], Spanish MICINN [MAT2011-22780] COST Action [CA18112]
COST Action [MP1103], PAT (Provincia Autonoma di Trento) project ENAM COST [CA18112]
Croatian Science foundation [4744] Croatian Science Foundation - European Union from the European Social Fund [PZS-2019-02-4129]
Croatian Science Foundation ["New Materials for Energy Storage"] [HRZZ-PKP-2016-6-4480] Croatian Science Foundation [PKP-2016-06-4480]
DESY [I-20181094 EC] Environmental Protection and Energy Efficiency Fund of Croatia
Environmental Protection and Energy Efficiency Fund of the Republic of Croatia European Union through the European Regional Development Fund within the Competitiveness and Cohesion Operational Programme [KK.01.1.1.06]
Ministry of Environment and Energy, Ministry of Science and Education, Environmental Protection and Energy Efficiency Fund, Croatian Science Foundation under the project New Materials for Energy Storage Ministry of Environment and Energy of Croatia
Ministry of Environment and Energy, the Ministry of Science and Education, the Environmental Protection and Energy Efficiency Fund, and the Croatian Science Foundation under the project "New Materials for Energy Storage" Ministry of Science and Education of Croatia
Ruđer Bošković Institute SAFU [KK.01.1.1.01.0001]
Spanish MICINN [IB2010SE-00191, MAT2011-22780]

Author's Bibliography

Mechanochemical modification of LiAlH4 with Fe2O3 - A combined DFT and experimental study

Dragojlović, Milijana; Milanović, Igor; Gradišek, Anton; Kurko, Sandra V.; Mitrić, Miodrag; Umićević, Ana; Radaković, Jana; Batalović, Katarina

(2021)

TY  - JOUR
AU  - Dragojlović, Milijana
AU  - Milanović, Igor
AU  - Gradišek, Anton
AU  - Kurko, Sandra V.
AU  - Mitrić, Miodrag
AU  - Umićević, Ana
AU  - Radaković, Jana
AU  - Batalović, Katarina
PY  - 2021
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/9091
AB  - LiAlH4 is a promising material for hydrogen storage, having the theoretical gravimetric density of 10.6 wt% H2. In order to decrease the temperature where hydrogen is released, we investigated the catalytic influence of Fe2O3 on LiAlH4 dehydrogenation, as a model case for understanding the effects transition oxide additives have in the catalysis process. Quick mechanochemical synthesis of LiAlH4 + 5 wt% Fe2O3 led to the significant decrease of the hydrogen desorption temperature, and desorption of over 7 wt%H2 in the temperature range 143–154 °C. Density functional theory (DFT)-based calculations with Tran-Blaha modified Becke-Johnson functional (TBmBJ) address the electronic structure of LiAlH4 and Li3AlH6. 57Fe Mössbauer study shows the change in the oxidational state of iron during hydrogen desorption, while the 1H NMR study reveals the presence of paramagnetic species that affect relaxation. The electron transfer from hydrides is discussed as the proposed mechanism of destabilization of LiAlH4 + 5 wt% Fe2O3. © 2021 Hydrogen Energy Publications LLC
T2  - International Journal of Hydrogen Energy
T1  - Mechanochemical modification of LiAlH4 with Fe2O3 - A combined DFT and experimental study
VL  - 46
IS  - 24
SP  - 13070
EP  - 13081
DO  - 10.1016/j.ijhydene.2021.01.086
ER  - 
@article{
author = "Dragojlović, Milijana and Milanović, Igor and Gradišek, Anton and Kurko, Sandra V. and Mitrić, Miodrag and Umićević, Ana and Radaković, Jana and Batalović, Katarina",
year = "2021",
abstract = "LiAlH4 is a promising material for hydrogen storage, having the theoretical gravimetric density of 10.6 wt% H2. In order to decrease the temperature where hydrogen is released, we investigated the catalytic influence of Fe2O3 on LiAlH4 dehydrogenation, as a model case for understanding the effects transition oxide additives have in the catalysis process. Quick mechanochemical synthesis of LiAlH4 + 5 wt% Fe2O3 led to the significant decrease of the hydrogen desorption temperature, and desorption of over 7 wt%H2 in the temperature range 143–154 °C. Density functional theory (DFT)-based calculations with Tran-Blaha modified Becke-Johnson functional (TBmBJ) address the electronic structure of LiAlH4 and Li3AlH6. 57Fe Mössbauer study shows the change in the oxidational state of iron during hydrogen desorption, while the 1H NMR study reveals the presence of paramagnetic species that affect relaxation. The electron transfer from hydrides is discussed as the proposed mechanism of destabilization of LiAlH4 + 5 wt% Fe2O3. © 2021 Hydrogen Energy Publications LLC",
journal = "International Journal of Hydrogen Energy",
title = "Mechanochemical modification of LiAlH4 with Fe2O3 - A combined DFT and experimental study",
volume = "46",
number = "24",
pages = "13070-13081",
doi = "10.1016/j.ijhydene.2021.01.086"
}
Dragojlović, M., Milanović, I., Gradišek, A., Kurko, S. V., Mitrić, M., Umićević, A., Radaković, J.,& Batalović, K.. (2021). Mechanochemical modification of LiAlH4 with Fe2O3 - A combined DFT and experimental study. in International Journal of Hydrogen Energy, 46(24), 13070-13081.
https://doi.org/10.1016/j.ijhydene.2021.01.086
Dragojlović M, Milanović I, Gradišek A, Kurko SV, Mitrić M, Umićević A, Radaković J, Batalović K. Mechanochemical modification of LiAlH4 with Fe2O3 - A combined DFT and experimental study. in International Journal of Hydrogen Energy. 2021;46(24):13070-13081.
doi:10.1016/j.ijhydene.2021.01.086 .
Dragojlović, Milijana, Milanović, Igor, Gradišek, Anton, Kurko, Sandra V., Mitrić, Miodrag, Umićević, Ana, Radaković, Jana, Batalović, Katarina, "Mechanochemical modification of LiAlH4 with Fe2O3 - A combined DFT and experimental study" in International Journal of Hydrogen Energy, 46, no. 24 (2021):13070-13081,
https://doi.org/10.1016/j.ijhydene.2021.01.086 . .

Mechanochemical modification of LiAlH4 with Fe2O3 - A combined DFT and experimental study

Dragojlović, Milijana; Milanović, Igor; Gradišek, Anton; Kurko, Sandra V.; Mitrić, Miodrag; Umićević, Ana; Radaković, Jana; Batalović, Katarina

(2021)

TY  - JOUR
AU  - Dragojlović, Milijana
AU  - Milanović, Igor
AU  - Gradišek, Anton
AU  - Kurko, Sandra V.
AU  - Mitrić, Miodrag
AU  - Umićević, Ana
AU  - Radaković, Jana
AU  - Batalović, Katarina
PY  - 2021
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/9087
AB  - LiAlH4 is a promising material for hydrogen storage, having the theoretical gravimetric density of 10.6 wt% H2. In order to decrease the temperature where hydrogen is released, we investigated the catalytic influence of Fe2O3 on LiAlH4 dehydrogenation, as a model case for understanding the effects transition oxide additives have in the catalysis process. Quick mechanochemical synthesis of LiAlH4 + 5 wt% Fe2O3 led to the significant decrease of the hydrogen desorption temperature, and desorption of over 7 wt%H2 in the temperature range 143–154 °C. Density functional theory (DFT)-based calculations with Tran-Blaha modified Becke-Johnson functional (TBmBJ) address the electronic structure of LiAlH4 and Li3AlH6. 57Fe Mössbauer study shows the change in the oxidational state of iron during hydrogen desorption, while the 1H NMR study reveals the presence of paramagnetic species that affect relaxation. The electron transfer from hydrides is discussed as the proposed mechanism of destabilization of LiAlH4 + 5 wt% Fe2O3. © 2021 Hydrogen Energy Publications LLC
T2  - International Journal of Hydrogen Energy
T1  - Mechanochemical modification of LiAlH4 with Fe2O3 - A combined DFT and experimental study
VL  - 46
IS  - 24
SP  - 13070
EP  - 13081
DO  - 10.1016/j.ijhydene.2021.01.086
ER  - 
@article{
author = "Dragojlović, Milijana and Milanović, Igor and Gradišek, Anton and Kurko, Sandra V. and Mitrić, Miodrag and Umićević, Ana and Radaković, Jana and Batalović, Katarina",
year = "2021",
abstract = "LiAlH4 is a promising material for hydrogen storage, having the theoretical gravimetric density of 10.6 wt% H2. In order to decrease the temperature where hydrogen is released, we investigated the catalytic influence of Fe2O3 on LiAlH4 dehydrogenation, as a model case for understanding the effects transition oxide additives have in the catalysis process. Quick mechanochemical synthesis of LiAlH4 + 5 wt% Fe2O3 led to the significant decrease of the hydrogen desorption temperature, and desorption of over 7 wt%H2 in the temperature range 143–154 °C. Density functional theory (DFT)-based calculations with Tran-Blaha modified Becke-Johnson functional (TBmBJ) address the electronic structure of LiAlH4 and Li3AlH6. 57Fe Mössbauer study shows the change in the oxidational state of iron during hydrogen desorption, while the 1H NMR study reveals the presence of paramagnetic species that affect relaxation. The electron transfer from hydrides is discussed as the proposed mechanism of destabilization of LiAlH4 + 5 wt% Fe2O3. © 2021 Hydrogen Energy Publications LLC",
journal = "International Journal of Hydrogen Energy",
title = "Mechanochemical modification of LiAlH4 with Fe2O3 - A combined DFT and experimental study",
volume = "46",
number = "24",
pages = "13070-13081",
doi = "10.1016/j.ijhydene.2021.01.086"
}
Dragojlović, M., Milanović, I., Gradišek, A., Kurko, S. V., Mitrić, M., Umićević, A., Radaković, J.,& Batalović, K.. (2021). Mechanochemical modification of LiAlH4 with Fe2O3 - A combined DFT and experimental study. in International Journal of Hydrogen Energy, 46(24), 13070-13081.
https://doi.org/10.1016/j.ijhydene.2021.01.086
Dragojlović M, Milanović I, Gradišek A, Kurko SV, Mitrić M, Umićević A, Radaković J, Batalović K. Mechanochemical modification of LiAlH4 with Fe2O3 - A combined DFT and experimental study. in International Journal of Hydrogen Energy. 2021;46(24):13070-13081.
doi:10.1016/j.ijhydene.2021.01.086 .
Dragojlović, Milijana, Milanović, Igor, Gradišek, Anton, Kurko, Sandra V., Mitrić, Miodrag, Umićević, Ana, Radaković, Jana, Batalović, Katarina, "Mechanochemical modification of LiAlH4 with Fe2O3 - A combined DFT and experimental study" in International Journal of Hydrogen Energy, 46, no. 24 (2021):13070-13081,
https://doi.org/10.1016/j.ijhydene.2021.01.086 . .

Mechanochemical Synthesis and Thermal Dehydrogenation of Novel Calcium-Containing Bimetallic Amidoboranes

Milanović, Igor; Biliškov, Nikola; Užarević, Krunoslav; Lukin, Stipe; Etter, Martin; Halasz, Ivan

(2021)

TY  - JOUR
AU  - Milanović, Igor
AU  - Biliškov, Nikola
AU  - Užarević, Krunoslav
AU  - Lukin, Stipe
AU  - Etter, Martin
AU  - Halasz, Ivan
PY  - 2021
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/9088
AB  - Metallic amidoboranes are widely investigated candidates for solid-state hydrogen storage, and much focus shifted recently toward bimetallic amidoboranes. Bimetallic amidoboranes are expected to introduce novel and enhanced physicochemical properties regarding storage and stability. However, these materials are still scarce and mostly grouped around magnesium- or aluminum-containing compounds. We present here a rapid and green mechanochemical solvent-free synthesis of two novel calcium-containing bimetallic amidoboranes, Li2Ca(NH2BH3)4 and Na2Ca(NH2BH3)4, from metal hydrides and ammonia borane. The insight into mechanochemical syntheses is provided by the in situ tandem synchrotron X-ray diffraction and thermal monitoring. The in situ data reveal how the choice of alkali metal hydride governs the course of reactions and their thermal profiles. In situ monitoring of thermal dehydrogenation of these materials is conducted by mass spectrometry and infrared spectroscopy, showing how the course of thermal decomposition varies depending on the structure of the amidoborane, resulting however in the same final products. These new hydrogen-rich bimetallic amidoboranes are structurally characterized by high-resolution powder X-ray diffraction, and they both show potential for hydrogen storage applications: high theoretical gravimetric capacities and low desorption temperatures of hydrogen without the significant presence of harmful gases. We also show how the choice of the milling reactor material can be decisive for the efficiency and overall success of the mechanochemical synthetic procedure, which may impact the design of milling syntheses for other thermally labile chemical systems. © 2021 American Chemical Society.
T2  - ACS Sustainable Chemistry & Engineering
T1  - Mechanochemical Synthesis and Thermal Dehydrogenation of Novel Calcium-Containing Bimetallic Amidoboranes
VL  - 9
IS  - 5
SP  - 2089
EP  - 2099
DO  - 10.1021/acssuschemeng.0c06839
ER  - 
@article{
author = "Milanović, Igor and Biliškov, Nikola and Užarević, Krunoslav and Lukin, Stipe and Etter, Martin and Halasz, Ivan",
year = "2021",
abstract = "Metallic amidoboranes are widely investigated candidates for solid-state hydrogen storage, and much focus shifted recently toward bimetallic amidoboranes. Bimetallic amidoboranes are expected to introduce novel and enhanced physicochemical properties regarding storage and stability. However, these materials are still scarce and mostly grouped around magnesium- or aluminum-containing compounds. We present here a rapid and green mechanochemical solvent-free synthesis of two novel calcium-containing bimetallic amidoboranes, Li2Ca(NH2BH3)4 and Na2Ca(NH2BH3)4, from metal hydrides and ammonia borane. The insight into mechanochemical syntheses is provided by the in situ tandem synchrotron X-ray diffraction and thermal monitoring. The in situ data reveal how the choice of alkali metal hydride governs the course of reactions and their thermal profiles. In situ monitoring of thermal dehydrogenation of these materials is conducted by mass spectrometry and infrared spectroscopy, showing how the course of thermal decomposition varies depending on the structure of the amidoborane, resulting however in the same final products. These new hydrogen-rich bimetallic amidoboranes are structurally characterized by high-resolution powder X-ray diffraction, and they both show potential for hydrogen storage applications: high theoretical gravimetric capacities and low desorption temperatures of hydrogen without the significant presence of harmful gases. We also show how the choice of the milling reactor material can be decisive for the efficiency and overall success of the mechanochemical synthetic procedure, which may impact the design of milling syntheses for other thermally labile chemical systems. © 2021 American Chemical Society.",
journal = "ACS Sustainable Chemistry & Engineering",
title = "Mechanochemical Synthesis and Thermal Dehydrogenation of Novel Calcium-Containing Bimetallic Amidoboranes",
volume = "9",
number = "5",
pages = "2089-2099",
doi = "10.1021/acssuschemeng.0c06839"
}
Milanović, I., Biliškov, N., Užarević, K., Lukin, S., Etter, M.,& Halasz, I.. (2021). Mechanochemical Synthesis and Thermal Dehydrogenation of Novel Calcium-Containing Bimetallic Amidoboranes. in ACS Sustainable Chemistry & Engineering, 9(5), 2089-2099.
https://doi.org/10.1021/acssuschemeng.0c06839
Milanović I, Biliškov N, Užarević K, Lukin S, Etter M, Halasz I. Mechanochemical Synthesis and Thermal Dehydrogenation of Novel Calcium-Containing Bimetallic Amidoboranes. in ACS Sustainable Chemistry & Engineering. 2021;9(5):2089-2099.
doi:10.1021/acssuschemeng.0c06839 .
Milanović, Igor, Biliškov, Nikola, Užarević, Krunoslav, Lukin, Stipe, Etter, Martin, Halasz, Ivan, "Mechanochemical Synthesis and Thermal Dehydrogenation of Novel Calcium-Containing Bimetallic Amidoboranes" in ACS Sustainable Chemistry & Engineering, 9, no. 5 (2021):2089-2099,
https://doi.org/10.1021/acssuschemeng.0c06839 . .
11

Mechanochemical Metathesis between AgNO3 and NaX (X = Cl, Br, I) and Ag2XNO3 Double-Salt Formation

Lukin, Stipe; Stolar, Tomislav; Lončarić, Ivor; Milanović, Igor; Biliškov, Nikola; Michiel, Marco di; Friščić, Tomislav; Halasz, Ivan

(2020)

TY  - JOUR
AU  - Lukin, Stipe
AU  - Stolar, Tomislav
AU  - Lončarić, Ivor
AU  - Milanović, Igor
AU  - Biliškov, Nikola
AU  - Michiel, Marco di
AU  - Friščić, Tomislav
AU  - Halasz, Ivan
PY  - 2020
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/9638
AB  - Here we describe real-time, in situ monitoring of mechanochemical solid-state metathesis between silver nitrate and the entire series of sodium halides, on the basis of tandem powder X-ray diffraction and Raman spectroscopy monitoring. The mechanistic monitoring reveals that reactions of AgNO3 with NaX (X = Cl, Br, I) differ in reaction paths, with only the reaction with NaBr providing the NaNO3 and AgX products directly. The reaction with NaI revealed the presence of a novel, short-lived intermediate phase, while the reaction with NaCl progressed the slowest through the well-defined Ag2ClNO3 intermediate double salt. While the corresponding iodide and bromide double salts were not observed as intermediates, all three are readily prepared as pure compounds by milling equimolar mixtures of AgX and AgNO3. The in situ observation of reactive intermediates in these simple metathesis reactions reveals a surprising resemblance of reactions involving purely ionic components to those of molecular organic solids and cocrystals. This study demonstrates the potential of in situ reaction monitoring for mechanochemical reactions of ionic compounds as well as completes the application of these techniques to all major compound classes.
T2  - Inorganic Chemistry
T1  - Mechanochemical Metathesis between AgNO3 and NaX (X = Cl, Br, I) and Ag2XNO3 Double-Salt Formation
VL  - 59
IS  - 17
SP  - 12200
EP  - 12208
DO  - 10.1021/acs.inorgchem.0c01196
ER  - 
@article{
author = "Lukin, Stipe and Stolar, Tomislav and Lončarić, Ivor and Milanović, Igor and Biliškov, Nikola and Michiel, Marco di and Friščić, Tomislav and Halasz, Ivan",
year = "2020",
abstract = "Here we describe real-time, in situ monitoring of mechanochemical solid-state metathesis between silver nitrate and the entire series of sodium halides, on the basis of tandem powder X-ray diffraction and Raman spectroscopy monitoring. The mechanistic monitoring reveals that reactions of AgNO3 with NaX (X = Cl, Br, I) differ in reaction paths, with only the reaction with NaBr providing the NaNO3 and AgX products directly. The reaction with NaI revealed the presence of a novel, short-lived intermediate phase, while the reaction with NaCl progressed the slowest through the well-defined Ag2ClNO3 intermediate double salt. While the corresponding iodide and bromide double salts were not observed as intermediates, all three are readily prepared as pure compounds by milling equimolar mixtures of AgX and AgNO3. The in situ observation of reactive intermediates in these simple metathesis reactions reveals a surprising resemblance of reactions involving purely ionic components to those of molecular organic solids and cocrystals. This study demonstrates the potential of in situ reaction monitoring for mechanochemical reactions of ionic compounds as well as completes the application of these techniques to all major compound classes.",
journal = "Inorganic Chemistry",
title = "Mechanochemical Metathesis between AgNO3 and NaX (X = Cl, Br, I) and Ag2XNO3 Double-Salt Formation",
volume = "59",
number = "17",
pages = "12200-12208",
doi = "10.1021/acs.inorgchem.0c01196"
}
Lukin, S., Stolar, T., Lončarić, I., Milanović, I., Biliškov, N., Michiel, M. d., Friščić, T.,& Halasz, I.. (2020). Mechanochemical Metathesis between AgNO3 and NaX (X = Cl, Br, I) and Ag2XNO3 Double-Salt Formation. in Inorganic Chemistry, 59(17), 12200-12208.
https://doi.org/10.1021/acs.inorgchem.0c01196
Lukin S, Stolar T, Lončarić I, Milanović I, Biliškov N, Michiel MD, Friščić T, Halasz I. Mechanochemical Metathesis between AgNO3 and NaX (X = Cl, Br, I) and Ag2XNO3 Double-Salt Formation. in Inorganic Chemistry. 2020;59(17):12200-12208.
doi:10.1021/acs.inorgchem.0c01196 .
Lukin, Stipe, Stolar, Tomislav, Lončarić, Ivor, Milanović, Igor, Biliškov, Nikola, Michiel, Marco di, Friščić, Tomislav, Halasz, Ivan, "Mechanochemical Metathesis between AgNO3 and NaX (X = Cl, Br, I) and Ag2XNO3 Double-Salt Formation" in Inorganic Chemistry, 59, no. 17 (2020):12200-12208,
https://doi.org/10.1021/acs.inorgchem.0c01196 . .
15
3
2

The influence of mechanical milling parameters on hydrogen desorption from Mgh2-Wo3 composites

Pantić, Tijana; Milanović, Igor; Lukić, Miodrag; Grbović-Novaković, Jasmina; Kurko, Sandra V.; Biliškov, Nikola; Milošević Govedarović, Sanja S.

(2020)

TY  - JOUR
AU  - Pantić, Tijana
AU  - Milanović, Igor
AU  - Lukić, Miodrag
AU  - Grbović-Novaković, Jasmina
AU  - Kurko, Sandra V.
AU  - Biliškov, Nikola
AU  - Milošević Govedarović, Sanja S.
PY  - 2020
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/8568
AB  - The influence of different milling conditions obtained using two high-energy mills on hydrogen desorption from MgH2-WO3 composites was investigated. The morphology, particle and crystallite size were studied as a function of milling speed, vial's volume, and ball-to-powder ratio. The vial's fill level, the number, and type of milling balls and additive's content kept constant. Changes in morphology and microstructure were correlated to desorption properties of materials. Higher milling speed reduced particle size but, there is no significant crystallite size reduction. On the other hand, additive distribution is similar regardless of the energy input. It has been noticed that different energy input on milling blend, which is the result of combined effects of above-mentioned factors, reflects on desorption temperature but not on the kinetics of desorption. In fact, desorption mechanism changes from 2D to 3D growth with constant nucleation rate, despite obtained changes in microstructure or chemical composition of the material. © 2019 Hydrogen Energy Publications LLC
T2  - International Journal of Hydrogen Energy
T1  - The influence of mechanical milling parameters on hydrogen desorption from Mgh2-Wo3 composites
VL  - 45
IS  - 14
SP  - 7901
EP  - 7911
DO  - 10.1016/j.ijhydene.2019.07.167
ER  - 
@article{
author = "Pantić, Tijana and Milanović, Igor and Lukić, Miodrag and Grbović-Novaković, Jasmina and Kurko, Sandra V. and Biliškov, Nikola and Milošević Govedarović, Sanja S.",
year = "2020",
abstract = "The influence of different milling conditions obtained using two high-energy mills on hydrogen desorption from MgH2-WO3 composites was investigated. The morphology, particle and crystallite size were studied as a function of milling speed, vial's volume, and ball-to-powder ratio. The vial's fill level, the number, and type of milling balls and additive's content kept constant. Changes in morphology and microstructure were correlated to desorption properties of materials. Higher milling speed reduced particle size but, there is no significant crystallite size reduction. On the other hand, additive distribution is similar regardless of the energy input. It has been noticed that different energy input on milling blend, which is the result of combined effects of above-mentioned factors, reflects on desorption temperature but not on the kinetics of desorption. In fact, desorption mechanism changes from 2D to 3D growth with constant nucleation rate, despite obtained changes in microstructure or chemical composition of the material. © 2019 Hydrogen Energy Publications LLC",
journal = "International Journal of Hydrogen Energy",
title = "The influence of mechanical milling parameters on hydrogen desorption from Mgh2-Wo3 composites",
volume = "45",
number = "14",
pages = "7901-7911",
doi = "10.1016/j.ijhydene.2019.07.167"
}
Pantić, T., Milanović, I., Lukić, M., Grbović-Novaković, J., Kurko, S. V., Biliškov, N.,& Milošević Govedarović, S. S.. (2020). The influence of mechanical milling parameters on hydrogen desorption from Mgh2-Wo3 composites. in International Journal of Hydrogen Energy, 45(14), 7901-7911.
https://doi.org/10.1016/j.ijhydene.2019.07.167
Pantić T, Milanović I, Lukić M, Grbović-Novaković J, Kurko SV, Biliškov N, Milošević Govedarović SS. The influence of mechanical milling parameters on hydrogen desorption from Mgh2-Wo3 composites. in International Journal of Hydrogen Energy. 2020;45(14):7901-7911.
doi:10.1016/j.ijhydene.2019.07.167 .
Pantić, Tijana, Milanović, Igor, Lukić, Miodrag, Grbović-Novaković, Jasmina, Kurko, Sandra V., Biliškov, Nikola, Milošević Govedarović, Sanja S., "The influence of mechanical milling parameters on hydrogen desorption from Mgh2-Wo3 composites" in International Journal of Hydrogen Energy, 45, no. 14 (2020):7901-7911,
https://doi.org/10.1016/j.ijhydene.2019.07.167 . .
1
1
1

Mechanochemical pretreatment of ammonia borane: A new procedure for sodium amidoborane synthesis

Milanović, Igor; Biliškov, Nikola

(2020)

TY  - JOUR
AU  - Milanović, Igor
AU  - Biliškov, Nikola
PY  - 2020
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/8564
AB  - The present work reports a new procedure for solid state synthesis of sodium amidoborane (NaAB) by mechanochemical (MC) reaction between as-received NaH and MC pretreated AB. Ball milling (BM) method was used for this purpose. First, pretreated AB was obtained by BM of as-received AB for 4.5 min. Second, powder of pretreated AB was mixed with as-received NaH and conducted to BM. Milling times were from 0 to 200 min: 5, 10, 30, 50, 100 and 200 min, respectively. By fixing the parameters of the milling conditions, only the influence of milling time on NaAB formation was followed. FTIR and XRD methods are used for analysis of powders after milling. We proved, by MC modification of pure AB, that the reaction rate between AB and NaH could be restricted to the interface between newly formed larger AB and small NaH particles. In such a way we obtained much better control of the reaction system with very accurate determination of reaction steps. Depending on the milling times, reaction process can be separated in three phases: i) 0–30 min phase - reactant and product are present; ii) 50–100 min phase - formed NaAB is almost without other pure; iii) 200 min phase - NaAB is totally decomposed. By this synthesis procedure we produced, for the first time, pure NaAB almost without any impurities. © 2019 Hydrogen Energy Publications LLC
T2  - International Journal of Hydrogen Energy
T1  - Mechanochemical pretreatment of ammonia borane: A new procedure for sodium amidoborane synthesis
VL  - 45
IS  - 14
SP  - 7938
EP  - 7946
DO  - 10.1016/j.ijhydene.2019.06.042
ER  - 
@article{
author = "Milanović, Igor and Biliškov, Nikola",
year = "2020",
abstract = "The present work reports a new procedure for solid state synthesis of sodium amidoborane (NaAB) by mechanochemical (MC) reaction between as-received NaH and MC pretreated AB. Ball milling (BM) method was used for this purpose. First, pretreated AB was obtained by BM of as-received AB for 4.5 min. Second, powder of pretreated AB was mixed with as-received NaH and conducted to BM. Milling times were from 0 to 200 min: 5, 10, 30, 50, 100 and 200 min, respectively. By fixing the parameters of the milling conditions, only the influence of milling time on NaAB formation was followed. FTIR and XRD methods are used for analysis of powders after milling. We proved, by MC modification of pure AB, that the reaction rate between AB and NaH could be restricted to the interface between newly formed larger AB and small NaH particles. In such a way we obtained much better control of the reaction system with very accurate determination of reaction steps. Depending on the milling times, reaction process can be separated in three phases: i) 0–30 min phase - reactant and product are present; ii) 50–100 min phase - formed NaAB is almost without other pure; iii) 200 min phase - NaAB is totally decomposed. By this synthesis procedure we produced, for the first time, pure NaAB almost without any impurities. © 2019 Hydrogen Energy Publications LLC",
journal = "International Journal of Hydrogen Energy",
title = "Mechanochemical pretreatment of ammonia borane: A new procedure for sodium amidoborane synthesis",
volume = "45",
number = "14",
pages = "7938-7946",
doi = "10.1016/j.ijhydene.2019.06.042"
}
Milanović, I.,& Biliškov, N.. (2020). Mechanochemical pretreatment of ammonia borane: A new procedure for sodium amidoborane synthesis. in International Journal of Hydrogen Energy, 45(14), 7938-7946.
https://doi.org/10.1016/j.ijhydene.2019.06.042
Milanović I, Biliškov N. Mechanochemical pretreatment of ammonia borane: A new procedure for sodium amidoborane synthesis. in International Journal of Hydrogen Energy. 2020;45(14):7938-7946.
doi:10.1016/j.ijhydene.2019.06.042 .
Milanović, Igor, Biliškov, Nikola, "Mechanochemical pretreatment of ammonia borane: A new procedure for sodium amidoborane synthesis" in International Journal of Hydrogen Energy, 45, no. 14 (2020):7938-7946,
https://doi.org/10.1016/j.ijhydene.2019.06.042 . .
4
3
4

Is WO3 catalyst for hydrogen desorption?

Marković, Smilja; Pantić, Tijana; Milanović, Igor; Lukić, Miodrag; Grbović-Novaković, Jasmina; Kurko, Sandra V.; Biliškov, Nikola; Milošević, Sanja S.

(Belgrade : Institute of Technical Sciences of SASA, 2017)

TY  - CONF
AU  - Pantić, Tijana
AU  - Milanović, Igor
AU  - Lukić, Miodrag
AU  - Grbović-Novaković, Jasmina
AU  - Kurko, Sandra V.
AU  - Biliškov, Nikola
AU  - Milošević, Sanja S.
PY  - 2017
UR  - http://itn.sanu.ac.rs/opus4/frontdoor/index/index/docId/1220
UR  - http://itn.sanu.ac.rs/opus4/files/1220/Pantic_16YRC2017.pdf
UR  - http://dais.sanu.ac.rs/123456789/15451
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/7559
AB  - Magnesium hydride, as hydrogen storage material, meets the requirements such as high gravimetric hydrogen capacity (7,6 wt%), low cost and weight, abundance and H2 absorption/desorption cycling possibility. Given that the oxide additives show the good impact on desorption properties, mechanical milling of MgH2 with addition of 5, 10 and 15% wt. WO3 was performed. The microstructure and morphology of composites were analysed by XRD, PSD and SEM and correlated to hydrogen desorption properties which have been investigated by DSC. The results have shown that WO3 has a positive effect on the desorption kinetics as well as on the change of the desorption mechanism.
PB  - Belgrade : Institute of Technical Sciences of SASA
C3  - Program and the Book of Abstracts / Sixteenth Young Researchers' Conference Materials Sciences and Engineering, December 6-8, 2017, Belgrade, Serbia
T1  - Is WO3 catalyst for hydrogen desorption?
SP  - 50
EP  - 50
ER  - 
@conference{
editor = "Marković, Smilja",
author = "Pantić, Tijana and Milanović, Igor and Lukić, Miodrag and Grbović-Novaković, Jasmina and Kurko, Sandra V. and Biliškov, Nikola and Milošević, Sanja S.",
year = "2017",
abstract = "Magnesium hydride, as hydrogen storage material, meets the requirements such as high gravimetric hydrogen capacity (7,6 wt%), low cost and weight, abundance and H2 absorption/desorption cycling possibility. Given that the oxide additives show the good impact on desorption properties, mechanical milling of MgH2 with addition of 5, 10 and 15% wt. WO3 was performed. The microstructure and morphology of composites were analysed by XRD, PSD and SEM and correlated to hydrogen desorption properties which have been investigated by DSC. The results have shown that WO3 has a positive effect on the desorption kinetics as well as on the change of the desorption mechanism.",
publisher = "Belgrade : Institute of Technical Sciences of SASA",
journal = "Program and the Book of Abstracts / Sixteenth Young Researchers' Conference Materials Sciences and Engineering, December 6-8, 2017, Belgrade, Serbia",
title = "Is WO3 catalyst for hydrogen desorption?",
pages = "50-50"
}
Marković, S., Pantić, T., Milanović, I., Lukić, M., Grbović-Novaković, J., Kurko, S. V., Biliškov, N.,& Milošević, S. S.. (2017). Is WO3 catalyst for hydrogen desorption?. in Program and the Book of Abstracts / Sixteenth Young Researchers' Conference Materials Sciences and Engineering, December 6-8, 2017, Belgrade, Serbia
Belgrade : Institute of Technical Sciences of SASA., 50-50.
Marković S, Pantić T, Milanović I, Lukić M, Grbović-Novaković J, Kurko SV, Biliškov N, Milošević SS. Is WO3 catalyst for hydrogen desorption?. in Program and the Book of Abstracts / Sixteenth Young Researchers' Conference Materials Sciences and Engineering, December 6-8, 2017, Belgrade, Serbia. 2017;:50-50..
Marković, Smilja, Pantić, Tijana, Milanović, Igor, Lukić, Miodrag, Grbović-Novaković, Jasmina, Kurko, Sandra V., Biliškov, Nikola, Milošević, Sanja S., "Is WO3 catalyst for hydrogen desorption?" in Program and the Book of Abstracts / Sixteenth Young Researchers' Conference Materials Sciences and Engineering, December 6-8, 2017, Belgrade, Serbia (2017):50-50.

In-Situ and Real-time Monitoring of Mechanochemical Preparation of Li2Mg(NH2BH3)(4) and Na2Mg(NH2BH3)(4) and Their Thermal Dehydrogenation

Biliskov, Nikola; Borgschulte, Andreas; Uzarevic, Krunoslav; Halasz, Ivan; Lukin, Stipe; Milošević, Sanja S.; Milanović, Igor; Grbović-Novaković, Jasmina

(2017)

TY  - JOUR
AU  - Biliskov, Nikola
AU  - Borgschulte, Andreas
AU  - Uzarevic, Krunoslav
AU  - Halasz, Ivan
AU  - Lukin, Stipe
AU  - Milošević, Sanja S.
AU  - Milanović, Igor
AU  - Grbović-Novaković, Jasmina
PY  - 2017
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/1870
AB  - For the first time, in situ monitoring of uninterrupted mechanochemical synthesis of two bimetallic amidoboranes, M2Mg(NH2BH3)(4) (M=Li, Na), by means of Raman spectroscopy, has been applied. This approach allowed real-time observation of key intermediate phases, and a straightforward follow-up of the reaction course. Detailed analysis of time-dependent spectra revealed a two-step mechanism through MNH2BH3 center dot NH3BH3 adducts as key intermediate phases which further reacted with MgH2, giving M2Mg(NH2BH3)(4) as final products. The intermediates partially take a competitive pathway toward the oligomeric M(BH3NH2BH2NH2BH3) phases. The crystal structure of the novel bimetallic amidoborane Li2Mg(NH2BH3)(4) was solved from high-resolution powder diffraction data and showed an analogous metal coordination to Na2Mg(NH2BH3)(4), but a significantly different crystal packing. Li2Mg(NH2BH3)(4) thermally dehydrogenates releasing highly pure H-2 in the amount of 7 wt.%, and at a lower temperature then its sodium analogue, making it significantly more viable for practical applications.
T2  - Chemistry. A European Journal
T1  - In-Situ and Real-time Monitoring of Mechanochemical Preparation of Li2Mg(NH2BH3)(4) and Na2Mg(NH2BH3)(4) and Their Thermal Dehydrogenation
VL  - 23
IS  - 64
SP  - 16274
EP  - 16282
DO  - 10.1002/chem.201702665
ER  - 
@article{
author = "Biliskov, Nikola and Borgschulte, Andreas and Uzarevic, Krunoslav and Halasz, Ivan and Lukin, Stipe and Milošević, Sanja S. and Milanović, Igor and Grbović-Novaković, Jasmina",
year = "2017",
abstract = "For the first time, in situ monitoring of uninterrupted mechanochemical synthesis of two bimetallic amidoboranes, M2Mg(NH2BH3)(4) (M=Li, Na), by means of Raman spectroscopy, has been applied. This approach allowed real-time observation of key intermediate phases, and a straightforward follow-up of the reaction course. Detailed analysis of time-dependent spectra revealed a two-step mechanism through MNH2BH3 center dot NH3BH3 adducts as key intermediate phases which further reacted with MgH2, giving M2Mg(NH2BH3)(4) as final products. The intermediates partially take a competitive pathway toward the oligomeric M(BH3NH2BH2NH2BH3) phases. The crystal structure of the novel bimetallic amidoborane Li2Mg(NH2BH3)(4) was solved from high-resolution powder diffraction data and showed an analogous metal coordination to Na2Mg(NH2BH3)(4), but a significantly different crystal packing. Li2Mg(NH2BH3)(4) thermally dehydrogenates releasing highly pure H-2 in the amount of 7 wt.%, and at a lower temperature then its sodium analogue, making it significantly more viable for practical applications.",
journal = "Chemistry. A European Journal",
title = "In-Situ and Real-time Monitoring of Mechanochemical Preparation of Li2Mg(NH2BH3)(4) and Na2Mg(NH2BH3)(4) and Their Thermal Dehydrogenation",
volume = "23",
number = "64",
pages = "16274-16282",
doi = "10.1002/chem.201702665"
}
Biliskov, N., Borgschulte, A., Uzarevic, K., Halasz, I., Lukin, S., Milošević, S. S., Milanović, I.,& Grbović-Novaković, J.. (2017). In-Situ and Real-time Monitoring of Mechanochemical Preparation of Li2Mg(NH2BH3)(4) and Na2Mg(NH2BH3)(4) and Their Thermal Dehydrogenation. in Chemistry. A European Journal, 23(64), 16274-16282.
https://doi.org/10.1002/chem.201702665
Biliskov N, Borgschulte A, Uzarevic K, Halasz I, Lukin S, Milošević SS, Milanović I, Grbović-Novaković J. In-Situ and Real-time Monitoring of Mechanochemical Preparation of Li2Mg(NH2BH3)(4) and Na2Mg(NH2BH3)(4) and Their Thermal Dehydrogenation. in Chemistry. A European Journal. 2017;23(64):16274-16282.
doi:10.1002/chem.201702665 .
Biliskov, Nikola, Borgschulte, Andreas, Uzarevic, Krunoslav, Halasz, Ivan, Lukin, Stipe, Milošević, Sanja S., Milanović, Igor, Grbović-Novaković, Jasmina, "In-Situ and Real-time Monitoring of Mechanochemical Preparation of Li2Mg(NH2BH3)(4) and Na2Mg(NH2BH3)(4) and Their Thermal Dehydrogenation" in Chemistry. A European Journal, 23, no. 64 (2017):16274-16282,
https://doi.org/10.1002/chem.201702665 . .
1
12
12
12

Sorption of pertechnetate onto ordered mesoporous carbon

Petrović, Đorđe; Ðukić, Anđelka; Kumrić, Ksenija; Milanović, Igor; Rašković-Lovre, Željka; Matović, Ljiljana

(Society of Physical Chemists of Serbia, 2014)

TY  - CONF
AU  - Petrović, Đorđe
AU  - Ðukić, Anđelka
AU  - Kumrić, Ksenija
AU  - Milanović, Igor
AU  - Rašković-Lovre, Željka
AU  - Matović, Ljiljana
PY  - 2014
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/9255
AB  - Ordered mesoporous carbon (OMC) was used as an adsorbent for the
removal of pertechnetate (TcO4
-) anion. Batch experiments were performed
to study the effects of pH and ionic strength of the solution. The adsorption
of TcO4
- is almost pH-independent in very wide pH region (from 4.0 to
10.0). Maximum distribution coefficient, Kd, was obtained at pH 2.0.
Adsorption of TcO4
- was not affected by the ionic strength changes.
PB  - Society of Physical Chemists of Serbia
C3  - PHYSICAL CHEMISTRY 2014: 12th International Conference on Fundamental and Applied Aspects of Physical Chemistry
T1  - Sorption of pertechnetate onto ordered mesoporous carbon
VL  - L-06-P
ER  - 
@conference{
author = "Petrović, Đorđe and Ðukić, Anđelka and Kumrić, Ksenija and Milanović, Igor and Rašković-Lovre, Željka and Matović, Ljiljana",
year = "2014",
abstract = "Ordered mesoporous carbon (OMC) was used as an adsorbent for the
removal of pertechnetate (TcO4
-) anion. Batch experiments were performed
to study the effects of pH and ionic strength of the solution. The adsorption
of TcO4
- is almost pH-independent in very wide pH region (from 4.0 to
10.0). Maximum distribution coefficient, Kd, was obtained at pH 2.0.
Adsorption of TcO4
- was not affected by the ionic strength changes.",
publisher = "Society of Physical Chemists of Serbia",
journal = "PHYSICAL CHEMISTRY 2014: 12th International Conference on Fundamental and Applied Aspects of Physical Chemistry",
title = "Sorption of pertechnetate onto ordered mesoporous carbon",
volume = "L-06-P"
}
Petrović, Đ., Ðukić, A., Kumrić, K., Milanović, I., Rašković-Lovre, Ž.,& Matović, L.. (2014). Sorption of pertechnetate onto ordered mesoporous carbon. in PHYSICAL CHEMISTRY 2014: 12th International Conference on Fundamental and Applied Aspects of Physical Chemistry
Society of Physical Chemists of Serbia., L-06-P.
Petrović Đ, Ðukić A, Kumrić K, Milanović I, Rašković-Lovre Ž, Matović L. Sorption of pertechnetate onto ordered mesoporous carbon. in PHYSICAL CHEMISTRY 2014: 12th International Conference on Fundamental and Applied Aspects of Physical Chemistry. 2014;L-06-P..
Petrović, Đorđe, Ðukić, Anđelka, Kumrić, Ksenija, Milanović, Igor, Rašković-Lovre, Željka, Matović, Ljiljana, "Sorption of pertechnetate onto ordered mesoporous carbon" in PHYSICAL CHEMISTRY 2014: 12th International Conference on Fundamental and Applied Aspects of Physical Chemistry, L-06-P (2014).

Investigation of surface and near-surface effects on hydrogen desorption kinetics of MgH2

Kurko, Sandra V.; Milanović, Igor; Grbović-Novaković, Jasmina; Ivanović, Nenad; Novaković, Nikola

(2014)

TY  - JOUR
AU  - Kurko, Sandra V.
AU  - Milanović, Igor
AU  - Grbović-Novaković, Jasmina
AU  - Ivanović, Nenad
AU  - Novaković, Nikola
PY  - 2014
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/5875
AB  - Desorption of hydrogen atoms from the (110) surface of rutile magnesium hydride (MgH2) was investigated using density functional theory (DFT) and pseudopotential method. System was represented by (110) (2x2) slab MgH2 supercell with 12 atomic layers along the z-axis. The H-desorption was modeled by the successive release of the four two-fold bonded H atoms from the (110) surface of MgH2. Dependence of the H-desorption energy on number and configuration of remaining surface hydrogen atoms has been determined. The features of the H atoms diffusion from the bulk towards the surface have been investigated, too. The results suggest that decrease in number of surface H atoms generally lowers the H-desorption energy in each desorption step and that both the H-H and the Mg-H interatomic interactions strongly influence the H-desorption process. The hydrogen vacancy formation energy in the first three sub-surface layers also exhibits a pronounced dependence on concentration. These findings lead to the conclusion that tendency of the MgH2 (110) surface to preserve a maximum possible surface H concentration in its most stable configuration is the limiting factor for the H-desorption kinetics. In principle, the obtained results allow us to determine preferred paths of surface and subsurface H-diffusion for a wide range of H concentrations and the principle features of the MgH2 dehydrogenation process, at least for the H-rich region. Being rather comprehensive, the approach is applicable for other metal hydrides, as well. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
T2  - International Journal of Hydrogen Energy
T1  - Investigation of surface and near-surface effects on hydrogen desorption kinetics of MgH2
VL  - 39
IS  - 2
SP  - 862
EP  - 867
DO  - 10.1016/j.ijhydene.2013.10.107
ER  - 
@article{
author = "Kurko, Sandra V. and Milanović, Igor and Grbović-Novaković, Jasmina and Ivanović, Nenad and Novaković, Nikola",
year = "2014",
abstract = "Desorption of hydrogen atoms from the (110) surface of rutile magnesium hydride (MgH2) was investigated using density functional theory (DFT) and pseudopotential method. System was represented by (110) (2x2) slab MgH2 supercell with 12 atomic layers along the z-axis. The H-desorption was modeled by the successive release of the four two-fold bonded H atoms from the (110) surface of MgH2. Dependence of the H-desorption energy on number and configuration of remaining surface hydrogen atoms has been determined. The features of the H atoms diffusion from the bulk towards the surface have been investigated, too. The results suggest that decrease in number of surface H atoms generally lowers the H-desorption energy in each desorption step and that both the H-H and the Mg-H interatomic interactions strongly influence the H-desorption process. The hydrogen vacancy formation energy in the first three sub-surface layers also exhibits a pronounced dependence on concentration. These findings lead to the conclusion that tendency of the MgH2 (110) surface to preserve a maximum possible surface H concentration in its most stable configuration is the limiting factor for the H-desorption kinetics. In principle, the obtained results allow us to determine preferred paths of surface and subsurface H-diffusion for a wide range of H concentrations and the principle features of the MgH2 dehydrogenation process, at least for the H-rich region. Being rather comprehensive, the approach is applicable for other metal hydrides, as well. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.",
journal = "International Journal of Hydrogen Energy",
title = "Investigation of surface and near-surface effects on hydrogen desorption kinetics of MgH2",
volume = "39",
number = "2",
pages = "862-867",
doi = "10.1016/j.ijhydene.2013.10.107"
}
Kurko, S. V., Milanović, I., Grbović-Novaković, J., Ivanović, N.,& Novaković, N.. (2014). Investigation of surface and near-surface effects on hydrogen desorption kinetics of MgH2. in International Journal of Hydrogen Energy, 39(2), 862-867.
https://doi.org/10.1016/j.ijhydene.2013.10.107
Kurko SV, Milanović I, Grbović-Novaković J, Ivanović N, Novaković N. Investigation of surface and near-surface effects on hydrogen desorption kinetics of MgH2. in International Journal of Hydrogen Energy. 2014;39(2):862-867.
doi:10.1016/j.ijhydene.2013.10.107 .
Kurko, Sandra V., Milanović, Igor, Grbović-Novaković, Jasmina, Ivanović, Nenad, Novaković, Nikola, "Investigation of surface and near-surface effects on hydrogen desorption kinetics of MgH2" in International Journal of Hydrogen Energy, 39, no. 2 (2014):862-867,
https://doi.org/10.1016/j.ijhydene.2013.10.107 . .
16
18
18

Near-surface hydrogen dynamics in titania

Vujasin, Radojka; Paskaš Mamula, Bojana; Milanović, Igor; Grbović-Novaković, Jasmina; Novaković, Nikola

(Society of Physical Chemists of Serbia, 2014)

TY  - CONF
AU  - Vujasin, Radojka
AU  - Paskaš Mamula, Bojana
AU  - Milanović, Igor
AU  - Grbović-Novaković, Jasmina
AU  - Novaković, Nikola
PY  - 2014
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/9220
AB  - The hydrogen interaction with the TiO2 (110) surface has been investigated
using pseudopotential and PAW methods with addition of U Hubbard term.
The hydrogen diffusion behavior and thermodynamic properties were
calculated by means of full relaxation of structure in every step of bulk
diffusion. The results show the existence of potential barriers close to every
atomic layer, the trends of barriers and overall system energy lowering away
from surface and the occurrence of preferential H sites within each
interlayer basin. These findings go in favor of previously experimental
findings of TiO2 low surface H coverage and observed easy diffusion of
hydrogen from reduced surface into the TiO2 bulk or at least in near surface
region.
PB  - Society of Physical Chemists of Serbia
C3  - PHYSICAL CHEMISTRY 2014: 12th International Conference on Fundamental and Applied Aspects of Physical Chemistry
T1  - Near-surface hydrogen dynamics in titania
VL  - I-07-P
ER  - 
@conference{
author = "Vujasin, Radojka and Paskaš Mamula, Bojana and Milanović, Igor and Grbović-Novaković, Jasmina and Novaković, Nikola",
year = "2014",
abstract = "The hydrogen interaction with the TiO2 (110) surface has been investigated
using pseudopotential and PAW methods with addition of U Hubbard term.
The hydrogen diffusion behavior and thermodynamic properties were
calculated by means of full relaxation of structure in every step of bulk
diffusion. The results show the existence of potential barriers close to every
atomic layer, the trends of barriers and overall system energy lowering away
from surface and the occurrence of preferential H sites within each
interlayer basin. These findings go in favor of previously experimental
findings of TiO2 low surface H coverage and observed easy diffusion of
hydrogen from reduced surface into the TiO2 bulk or at least in near surface
region.",
publisher = "Society of Physical Chemists of Serbia",
journal = "PHYSICAL CHEMISTRY 2014: 12th International Conference on Fundamental and Applied Aspects of Physical Chemistry",
title = "Near-surface hydrogen dynamics in titania",
volume = "I-07-P"
}
Vujasin, R., Paskaš Mamula, B., Milanović, I., Grbović-Novaković, J.,& Novaković, N.. (2014). Near-surface hydrogen dynamics in titania. in PHYSICAL CHEMISTRY 2014: 12th International Conference on Fundamental and Applied Aspects of Physical Chemistry
Society of Physical Chemists of Serbia., I-07-P.
Vujasin R, Paskaš Mamula B, Milanović I, Grbović-Novaković J, Novaković N. Near-surface hydrogen dynamics in titania. in PHYSICAL CHEMISTRY 2014: 12th International Conference on Fundamental and Applied Aspects of Physical Chemistry. 2014;I-07-P..
Vujasin, Radojka, Paskaš Mamula, Bojana, Milanović, Igor, Grbović-Novaković, Jasmina, Novaković, Nikola, "Near-surface hydrogen dynamics in titania" in PHYSICAL CHEMISTRY 2014: 12th International Conference on Fundamental and Applied Aspects of Physical Chemistry, I-07-P (2014).

Surface characterisation of mechanochemicaly activated carbon cloth

Đukić, Anđelka B.; Grbović-Novaković, Jasmina; Stojanović, Zoran S.; Milanović, Igor; Vujasin, Radojka; Milošević, Sanja S.; Matović, Ljiljana

(Belgrade : Materials Research Society of Serbia, 2013)

TY  - CONF
AU  - Đukić, Anđelka B.
AU  - Grbović-Novaković, Jasmina
AU  - Stojanović, Zoran S.
AU  - Milanović, Igor
AU  - Vujasin, Radojka
AU  - Milošević, Sanja S.
AU  - Matović, Ljiljana
PY  - 2013
UR  - http://www.itn.sanu.ac.rs/opus4/frontdoor/index/index/docId/651
UR  - http://dais.sanu.ac.rs/123456789/390
UR  - http://www.itn.sanu.ac.rs/opus4/files/651/Djukic_YUCOMAT2013_126.pdf
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/7414
AB  - Adsorption on activated carbon cloth is an efficient procedure for removing pollutants from wastewaters, because this material possesses large specific area and high adsorption capacity. Inthis study the activated carbon cloth was modified by mechanical milling in order to improve its sorption properties. The microstructure and morphology of the sample was investigated by XRD,PSD and SEM and surface chemistry was characterized by potentiometric titrations. The result showed that microstructure and morphology was drastically changed with milling: particle sizesreduction, agglomeration and the loss of fibrous structure occurred. These changes resulted in increase of the acidic and the base groups: the number of basic groups was increased by the factor of 11 while the number of acidic groups by the factor of 1.5.
PB  - Belgrade : Materials Research Society of Serbia
C3  - The Fifteenth Annual Conference YUCOMAT 2013: Programme and the Book of Abstracts
T1  - Surface characterisation of mechanochemicaly activated carbon cloth
SP  - 126
EP  - 126
ER  - 
@conference{
author = "Đukić, Anđelka B. and Grbović-Novaković, Jasmina and Stojanović, Zoran S. and Milanović, Igor and Vujasin, Radojka and Milošević, Sanja S. and Matović, Ljiljana",
year = "2013",
abstract = "Adsorption on activated carbon cloth is an efficient procedure for removing pollutants from wastewaters, because this material possesses large specific area and high adsorption capacity. Inthis study the activated carbon cloth was modified by mechanical milling in order to improve its sorption properties. The microstructure and morphology of the sample was investigated by XRD,PSD and SEM and surface chemistry was characterized by potentiometric titrations. The result showed that microstructure and morphology was drastically changed with milling: particle sizesreduction, agglomeration and the loss of fibrous structure occurred. These changes resulted in increase of the acidic and the base groups: the number of basic groups was increased by the factor of 11 while the number of acidic groups by the factor of 1.5.",
publisher = "Belgrade : Materials Research Society of Serbia",
journal = "The Fifteenth Annual Conference YUCOMAT 2013: Programme and the Book of Abstracts",
title = "Surface characterisation of mechanochemicaly activated carbon cloth",
pages = "126-126"
}
Đukić, A. B., Grbović-Novaković, J., Stojanović, Z. S., Milanović, I., Vujasin, R., Milošević, S. S.,& Matović, L.. (2013). Surface characterisation of mechanochemicaly activated carbon cloth. in The Fifteenth Annual Conference YUCOMAT 2013: Programme and the Book of Abstracts
Belgrade : Materials Research Society of Serbia., 126-126.
Đukić AB, Grbović-Novaković J, Stojanović ZS, Milanović I, Vujasin R, Milošević SS, Matović L. Surface characterisation of mechanochemicaly activated carbon cloth. in The Fifteenth Annual Conference YUCOMAT 2013: Programme and the Book of Abstracts. 2013;:126-126..
Đukić, Anđelka B., Grbović-Novaković, Jasmina, Stojanović, Zoran S., Milanović, Igor, Vujasin, Radojka, Milošević, Sanja S., Matović, Ljiljana, "Surface characterisation of mechanochemicaly activated carbon cloth" in The Fifteenth Annual Conference YUCOMAT 2013: Programme and the Book of Abstracts (2013):126-126.

Changes in Storage Properties of Hydrides Induced by Ion Irradiation

Grbović-Novaković, Jasmina; Kurko, Sandra V.; Rašković-Lovre, Željka; Milošević, Sanja S.; Milanović, Igor; Stojanović, Zoran S.; Vujasin, Radojka; Matović, Ljiljana

(2013)

TY  - JOUR
AU  - Grbović-Novaković, Jasmina
AU  - Kurko, Sandra V.
AU  - Rašković-Lovre, Željka
AU  - Milošević, Sanja S.
AU  - Milanović, Igor
AU  - Stojanović, Zoran S.
AU  - Vujasin, Radojka
AU  - Matović, Ljiljana
PY  - 2013
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/5536
AB  - The influence of structural changes caused by irradiation with different ions, their energies and fluences on sorption properties has been investigated. The irradiation has been done using B3+ and N3+ ions at 45 keV with ion fluence of 10(16) ion/cm(2) at the FAMA ion source at Vinca Institute of Nuclear Sciences in Belgrade. Morphology and microstructure of samples were analysed using XRD and particle size analysis, while estimation of penetration depth and deposition of defects were done by SRIM calculations. Hydrogen desorption properties and kinetics were evaluated from TPD measurements and numerical non-isothermal procedure. Results suggest that there are several mechanisms of desorption depending on defect concentration, their interaction and ordering. It has been also demonstrated that the changes in near-surface area play the crucial role in hydrogen desorption kinetics. It is confirmed that there is possibility to control the thermodynamic parameters of these systems by controlling vacancies depth profile and concentration.
T2  - Materials Science - Medziagotyra
T1  - Changes in Storage Properties of Hydrides Induced by Ion Irradiation
VL  - 19
IS  - 2
SP  - 134
EP  - 139
DO  - 10.5755/j01.ms.19.2.1579
ER  - 
@article{
author = "Grbović-Novaković, Jasmina and Kurko, Sandra V. and Rašković-Lovre, Željka and Milošević, Sanja S. and Milanović, Igor and Stojanović, Zoran S. and Vujasin, Radojka and Matović, Ljiljana",
year = "2013",
abstract = "The influence of structural changes caused by irradiation with different ions, their energies and fluences on sorption properties has been investigated. The irradiation has been done using B3+ and N3+ ions at 45 keV with ion fluence of 10(16) ion/cm(2) at the FAMA ion source at Vinca Institute of Nuclear Sciences in Belgrade. Morphology and microstructure of samples were analysed using XRD and particle size analysis, while estimation of penetration depth and deposition of defects were done by SRIM calculations. Hydrogen desorption properties and kinetics were evaluated from TPD measurements and numerical non-isothermal procedure. Results suggest that there are several mechanisms of desorption depending on defect concentration, their interaction and ordering. It has been also demonstrated that the changes in near-surface area play the crucial role in hydrogen desorption kinetics. It is confirmed that there is possibility to control the thermodynamic parameters of these systems by controlling vacancies depth profile and concentration.",
journal = "Materials Science - Medziagotyra",
title = "Changes in Storage Properties of Hydrides Induced by Ion Irradiation",
volume = "19",
number = "2",
pages = "134-139",
doi = "10.5755/j01.ms.19.2.1579"
}
Grbović-Novaković, J., Kurko, S. V., Rašković-Lovre, Ž., Milošević, S. S., Milanović, I., Stojanović, Z. S., Vujasin, R.,& Matović, L.. (2013). Changes in Storage Properties of Hydrides Induced by Ion Irradiation. in Materials Science - Medziagotyra, 19(2), 134-139.
https://doi.org/10.5755/j01.ms.19.2.1579
Grbović-Novaković J, Kurko SV, Rašković-Lovre Ž, Milošević SS, Milanović I, Stojanović ZS, Vujasin R, Matović L. Changes in Storage Properties of Hydrides Induced by Ion Irradiation. in Materials Science - Medziagotyra. 2013;19(2):134-139.
doi:10.5755/j01.ms.19.2.1579 .
Grbović-Novaković, Jasmina, Kurko, Sandra V., Rašković-Lovre, Željka, Milošević, Sanja S., Milanović, Igor, Stojanović, Zoran S., Vujasin, Radojka, Matović, Ljiljana, "Changes in Storage Properties of Hydrides Induced by Ion Irradiation" in Materials Science - Medziagotyra, 19, no. 2 (2013):134-139,
https://doi.org/10.5755/j01.ms.19.2.1579 . .
1
2
2

Changes in kinetic parameters of decomposition of MgH2 destabilized by irradiation with C2+ ions

Kurko, Sandra V.; Milanović, Igor; Milošević, Sanja S.; Rašković-Lovre, Željka; Fernandez, Jose Francisco; Ares Fernandez, Jose Ramon; Matović, Ljiljana; Grbović-Novaković, Jasmina

(2013)

TY  - JOUR
AU  - Kurko, Sandra V.
AU  - Milanović, Igor
AU  - Milošević, Sanja S.
AU  - Rašković-Lovre, Željka
AU  - Fernandez, Jose Francisco
AU  - Ares Fernandez, Jose Ramon
AU  - Matović, Ljiljana
AU  - Grbović-Novaković, Jasmina
PY  - 2013
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/5691
AB  - In attempt to improve desorption behaviour of MgH2, the influence of well-defined structural changes induced within a thin surface layer of MgH2 have been investigated. The defects were induced by 30 key C2+ ions irradiation using different fluencies ranging from 10(12)-10(16) ions/cm(2). The hydrogen desorption properties were investigated by thermal desorption spectroscopy analysis (TDS), while kinetics parameters were deduced using non-isothermal kinetic approach. The existence of multiple TDS peaks and different curve shapes indicate difference in desorption mechanism. To understand changes in the rate limiting step, shapes of all desorption peaks have been analyzed using different kinetic models. Regarding the irradiated sample, the function based on Avrami-Erofeev model with n = 4 gives the best fit over theta range from 0.3 to 0.8 while for untreated sample the best fit is obtained for Avrami-Erofeev model with n = 3. The change in mechanism can be attributed to the different way of nuclei growth. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
T2  - International Journal of Hydrogen Energy
T1  - Changes in kinetic parameters of decomposition of MgH2 destabilized by irradiation with C2+ ions
VL  - 38
IS  - 27
SP  - 12199
EP  - 12206
DO  - 10.1016/j.ijhydene.2013.05.132
ER  - 
@article{
author = "Kurko, Sandra V. and Milanović, Igor and Milošević, Sanja S. and Rašković-Lovre, Željka and Fernandez, Jose Francisco and Ares Fernandez, Jose Ramon and Matović, Ljiljana and Grbović-Novaković, Jasmina",
year = "2013",
abstract = "In attempt to improve desorption behaviour of MgH2, the influence of well-defined structural changes induced within a thin surface layer of MgH2 have been investigated. The defects were induced by 30 key C2+ ions irradiation using different fluencies ranging from 10(12)-10(16) ions/cm(2). The hydrogen desorption properties were investigated by thermal desorption spectroscopy analysis (TDS), while kinetics parameters were deduced using non-isothermal kinetic approach. The existence of multiple TDS peaks and different curve shapes indicate difference in desorption mechanism. To understand changes in the rate limiting step, shapes of all desorption peaks have been analyzed using different kinetic models. Regarding the irradiated sample, the function based on Avrami-Erofeev model with n = 4 gives the best fit over theta range from 0.3 to 0.8 while for untreated sample the best fit is obtained for Avrami-Erofeev model with n = 3. The change in mechanism can be attributed to the different way of nuclei growth. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.",
journal = "International Journal of Hydrogen Energy",
title = "Changes in kinetic parameters of decomposition of MgH2 destabilized by irradiation with C2+ ions",
volume = "38",
number = "27",
pages = "12199-12206",
doi = "10.1016/j.ijhydene.2013.05.132"
}
Kurko, S. V., Milanović, I., Milošević, S. S., Rašković-Lovre, Ž., Fernandez, J. F., Ares Fernandez, J. R., Matović, L.,& Grbović-Novaković, J.. (2013). Changes in kinetic parameters of decomposition of MgH2 destabilized by irradiation with C2+ ions. in International Journal of Hydrogen Energy, 38(27), 12199-12206.
https://doi.org/10.1016/j.ijhydene.2013.05.132
Kurko SV, Milanović I, Milošević SS, Rašković-Lovre Ž, Fernandez JF, Ares Fernandez JR, Matović L, Grbović-Novaković J. Changes in kinetic parameters of decomposition of MgH2 destabilized by irradiation with C2+ ions. in International Journal of Hydrogen Energy. 2013;38(27):12199-12206.
doi:10.1016/j.ijhydene.2013.05.132 .
Kurko, Sandra V., Milanović, Igor, Milošević, Sanja S., Rašković-Lovre, Željka, Fernandez, Jose Francisco, Ares Fernandez, Jose Ramon, Matović, Ljiljana, Grbović-Novaković, Jasmina, "Changes in kinetic parameters of decomposition of MgH2 destabilized by irradiation with C2+ ions" in International Journal of Hydrogen Energy, 38, no. 27 (2013):12199-12206,
https://doi.org/10.1016/j.ijhydene.2013.05.132 . .
3
3
3

Aging Effects in Irradiated MgH2; Connection to Hydrogen Production

Kurko, Sandra V.; Matović, Ljiljana; Vujasin, Radojka; Milanović, Igor; Rašković-Lovre, Željka; Ivanović, Nenad; Grbović-Novaković, Jasmina

(2013)

TY  - JOUR
AU  - Kurko, Sandra V.
AU  - Matović, Ljiljana
AU  - Vujasin, Radojka
AU  - Milanović, Igor
AU  - Rašković-Lovre, Željka
AU  - Ivanović, Nenad
AU  - Grbović-Novaković, Jasmina
PY  - 2013
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/5711
AB  - The paper deals with the possibility to control aging of MgH2 by controlling the deposited energy, number and type of defects and their distribution in the near surface region using Ar8+, Xe8+, and B3+ ion irradiation. The evolution of the obtained phases was monitored using X-ray diffraction (XRD), scanning electron microscopy (SEM), Raman spectroscopy, laser scattering particle size distribution measurements and surface area analyses. Obtained results give the possibility to resolve between the material related (impurities, defects, strains) and the ambient induced component of aging.
T2  - Materials Science - Medziagotyra
T1  - Aging Effects in Irradiated MgH2; Connection to Hydrogen Production
VL  - 19
IS  - 3
SP  - 349
EP  - 353
DO  - 10.5755/j01.ms.19.3.2308
ER  - 
@article{
author = "Kurko, Sandra V. and Matović, Ljiljana and Vujasin, Radojka and Milanović, Igor and Rašković-Lovre, Željka and Ivanović, Nenad and Grbović-Novaković, Jasmina",
year = "2013",
abstract = "The paper deals with the possibility to control aging of MgH2 by controlling the deposited energy, number and type of defects and their distribution in the near surface region using Ar8+, Xe8+, and B3+ ion irradiation. The evolution of the obtained phases was monitored using X-ray diffraction (XRD), scanning electron microscopy (SEM), Raman spectroscopy, laser scattering particle size distribution measurements and surface area analyses. Obtained results give the possibility to resolve between the material related (impurities, defects, strains) and the ambient induced component of aging.",
journal = "Materials Science - Medziagotyra",
title = "Aging Effects in Irradiated MgH2; Connection to Hydrogen Production",
volume = "19",
number = "3",
pages = "349-353",
doi = "10.5755/j01.ms.19.3.2308"
}
Kurko, S. V., Matović, L., Vujasin, R., Milanović, I., Rašković-Lovre, Ž., Ivanović, N.,& Grbović-Novaković, J.. (2013). Aging Effects in Irradiated MgH2; Connection to Hydrogen Production. in Materials Science - Medziagotyra, 19(3), 349-353.
https://doi.org/10.5755/j01.ms.19.3.2308
Kurko SV, Matović L, Vujasin R, Milanović I, Rašković-Lovre Ž, Ivanović N, Grbović-Novaković J. Aging Effects in Irradiated MgH2; Connection to Hydrogen Production. in Materials Science - Medziagotyra. 2013;19(3):349-353.
doi:10.5755/j01.ms.19.3.2308 .
Kurko, Sandra V., Matović, Ljiljana, Vujasin, Radojka, Milanović, Igor, Rašković-Lovre, Željka, Ivanović, Nenad, Grbović-Novaković, Jasmina, "Aging Effects in Irradiated MgH2; Connection to Hydrogen Production" in Materials Science - Medziagotyra, 19, no. 3 (2013):349-353,
https://doi.org/10.5755/j01.ms.19.3.2308 . .
1
1
1

Hydrogen desorption properties of MgH2 catalysed with NaNH2

Milošević, Sanja S.; Milanović, Igor; Paskaš Mamula, Bojana; Đukić, Anđelka B.; Rajnović, Dragan; Pasquini, Luca; Grbović-Novaković, Jasmina

(2013)

TY  - JOUR
AU  - Milošević, Sanja S.
AU  - Milanović, Igor
AU  - Paskaš Mamula, Bojana
AU  - Đukić, Anđelka B.
AU  - Rajnović, Dragan
AU  - Pasquini, Luca
AU  - Grbović-Novaković, Jasmina
PY  - 2013
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/5692
AB  - To improve hydrogen desorption properties of MgH2, mechanical milling of MgH2 with low concentration (2 and 5%) of NaNH2 has been performed. Pre-milling of MgH2 for 10 h has been done and then six samples have been synthesised with different milling times from 15 to 60 min. Microstructural characterisation has been performed using X-ray diffraction (XRD), scanning electron microscopy (SEM) and laser scattering measurements (PSD), and correlated to desorption properties examined using Differential Scanning Calorimetry (DSC) and Hydrogen Sorption Analyser (HSA). Thermal analysis shows that desorption temperatures are shifted towards lower values. It also highlights the significance of milling time and additive concentration on desorption behaviour. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
T2  - International Journal of Hydrogen Energy
T1  - Hydrogen desorption properties of MgH2 catalysed with NaNH2
VL  - 38
IS  - 27
SP  - 12223
EP  - 12229
DO  - 10.1016/j.ijhydene.2013.06.083
ER  - 
@article{
author = "Milošević, Sanja S. and Milanović, Igor and Paskaš Mamula, Bojana and Đukić, Anđelka B. and Rajnović, Dragan and Pasquini, Luca and Grbović-Novaković, Jasmina",
year = "2013",
abstract = "To improve hydrogen desorption properties of MgH2, mechanical milling of MgH2 with low concentration (2 and 5%) of NaNH2 has been performed. Pre-milling of MgH2 for 10 h has been done and then six samples have been synthesised with different milling times from 15 to 60 min. Microstructural characterisation has been performed using X-ray diffraction (XRD), scanning electron microscopy (SEM) and laser scattering measurements (PSD), and correlated to desorption properties examined using Differential Scanning Calorimetry (DSC) and Hydrogen Sorption Analyser (HSA). Thermal analysis shows that desorption temperatures are shifted towards lower values. It also highlights the significance of milling time and additive concentration on desorption behaviour. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.",
journal = "International Journal of Hydrogen Energy",
title = "Hydrogen desorption properties of MgH2 catalysed with NaNH2",
volume = "38",
number = "27",
pages = "12223-12229",
doi = "10.1016/j.ijhydene.2013.06.083"
}
Milošević, S. S., Milanović, I., Paskaš Mamula, B., Đukić, A. B., Rajnović, D., Pasquini, L.,& Grbović-Novaković, J.. (2013). Hydrogen desorption properties of MgH2 catalysed with NaNH2. in International Journal of Hydrogen Energy, 38(27), 12223-12229.
https://doi.org/10.1016/j.ijhydene.2013.06.083
Milošević SS, Milanović I, Paskaš Mamula B, Đukić AB, Rajnović D, Pasquini L, Grbović-Novaković J. Hydrogen desorption properties of MgH2 catalysed with NaNH2. in International Journal of Hydrogen Energy. 2013;38(27):12223-12229.
doi:10.1016/j.ijhydene.2013.06.083 .
Milošević, Sanja S., Milanović, Igor, Paskaš Mamula, Bojana, Đukić, Anđelka B., Rajnović, Dragan, Pasquini, Luca, Grbović-Novaković, Jasmina, "Hydrogen desorption properties of MgH2 catalysed with NaNH2" in International Journal of Hydrogen Energy, 38, no. 27 (2013):12223-12229,
https://doi.org/10.1016/j.ijhydene.2013.06.083 . .
11
11
11

Hydrogen desorption properties of MgH2/LiAlH4 composites

Milanović, Igor; Milošević, Sanja S.; Matović, Ljiljana; Vujasin, Radojka; Nauakovic, Nikola; Checchetto, Riccardo; Grbović-Novaković, Jasmina

(2013)

TY  - JOUR
AU  - Milanović, Igor
AU  - Milošević, Sanja S.
AU  - Matović, Ljiljana
AU  - Vujasin, Radojka
AU  - Nauakovic, Nikola
AU  - Checchetto, Riccardo
AU  - Grbović-Novaković, Jasmina
PY  - 2013
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/5690
AB  - The hydrogen desorption properties of MgH2-LiAlH4 composites obtained by mechanical milling for different milling times have been investigated by Thermal Desorption Spectroscopy (TDS) and correlated to the sample microstructure and morphology analysed by X-ray Diffraction (XRD) and Scanning Electron Microscopy (SEM). The MgH2-LiAlH4 composites show improved hydrogen desorption properties in comparison with both as-received and ball-milled MgH2. Mixing of MgH2 with small amount of LiAlH4 (5 wt.%) using short mechanical milling (15 min) shifts, in fact, the hydrogen desorption peak to lower temperature than those observed with both as-received and milled MgH2 samples. Longer mixing times of the MgH2-LiAlH4 composites (30 and 60 mm) reduce the catalytic activity of the LiAlH4 additive as revealed by the shift of the hydrogen desorption peak to higher temperatures. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
T2  - International Journal of Hydrogen Energy
T1  - Hydrogen desorption properties of MgH2/LiAlH4 composites
VL  - 38
IS  - 27
SP  - 12152
EP  - 12158
DO  - 10.1016/j.ijhydene.2013.05.020
ER  - 
@article{
author = "Milanović, Igor and Milošević, Sanja S. and Matović, Ljiljana and Vujasin, Radojka and Nauakovic, Nikola and Checchetto, Riccardo and Grbović-Novaković, Jasmina",
year = "2013",
abstract = "The hydrogen desorption properties of MgH2-LiAlH4 composites obtained by mechanical milling for different milling times have been investigated by Thermal Desorption Spectroscopy (TDS) and correlated to the sample microstructure and morphology analysed by X-ray Diffraction (XRD) and Scanning Electron Microscopy (SEM). The MgH2-LiAlH4 composites show improved hydrogen desorption properties in comparison with both as-received and ball-milled MgH2. Mixing of MgH2 with small amount of LiAlH4 (5 wt.%) using short mechanical milling (15 min) shifts, in fact, the hydrogen desorption peak to lower temperature than those observed with both as-received and milled MgH2 samples. Longer mixing times of the MgH2-LiAlH4 composites (30 and 60 mm) reduce the catalytic activity of the LiAlH4 additive as revealed by the shift of the hydrogen desorption peak to higher temperatures. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.",
journal = "International Journal of Hydrogen Energy",
title = "Hydrogen desorption properties of MgH2/LiAlH4 composites",
volume = "38",
number = "27",
pages = "12152-12158",
doi = "10.1016/j.ijhydene.2013.05.020"
}
Milanović, I., Milošević, S. S., Matović, L., Vujasin, R., Nauakovic, N., Checchetto, R.,& Grbović-Novaković, J.. (2013). Hydrogen desorption properties of MgH2/LiAlH4 composites. in International Journal of Hydrogen Energy, 38(27), 12152-12158.
https://doi.org/10.1016/j.ijhydene.2013.05.020
Milanović I, Milošević SS, Matović L, Vujasin R, Nauakovic N, Checchetto R, Grbović-Novaković J. Hydrogen desorption properties of MgH2/LiAlH4 composites. in International Journal of Hydrogen Energy. 2013;38(27):12152-12158.
doi:10.1016/j.ijhydene.2013.05.020 .
Milanović, Igor, Milošević, Sanja S., Matović, Ljiljana, Vujasin, Radojka, Nauakovic, Nikola, Checchetto, Riccardo, Grbović-Novaković, Jasmina, "Hydrogen desorption properties of MgH2/LiAlH4 composites" in International Journal of Hydrogen Energy, 38, no. 27 (2013):12152-12158,
https://doi.org/10.1016/j.ijhydene.2013.05.020 . .
13
12
15

Microstructure and hydrogen storage properties of MgH2-TiB2-SiC composites

Milanović, Igor; Milošević, Sanja S.; Rašković-Lovre, Željka; Novaković, Nikola; Vujasin, Radojka; Matović, Ljiljana; Fernandez, Jose Francisco; Sanchez, Carlos; Grbović-Novaković, Jasmina

(2013)

TY  - JOUR
AU  - Milanović, Igor
AU  - Milošević, Sanja S.
AU  - Rašković-Lovre, Željka
AU  - Novaković, Nikola
AU  - Vujasin, Radojka
AU  - Matović, Ljiljana
AU  - Fernandez, Jose Francisco
AU  - Sanchez, Carlos
AU  - Grbović-Novaković, Jasmina
PY  - 2013
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/5465
AB  - The influence of TiB2 and SiC ceramics on H-desorption kinetics from MgH2 based composites was investigated and correlated with the microstructure and morphology of the composites. The mechanism of desorption and the activation energy for desorption was investigated by applying non-isothermal kinetic analysis of thermodesorption spectra. It has been shown that TiB2 addition leads to significant decrease of the activation energy for desorption, while SiC addition has effect on the interface reaction between hydride and hydroxide. The mechanism of desorption change from Avrami-Erofeev n=3 for pure MgH2 to Avrami Erofeev n=4 for composite materials. The change from 3 to 4 can be due to the modification of the nucleation process or a change in the dimensionality of the growth. Those high values of n discard a diffusion control as a rate limiting step. (C) 2012 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
T2  - Ceramics International
T1  - Microstructure and hydrogen storage properties of MgH2-TiB2-SiC composites
VL  - 39
IS  - 4
SP  - 4399
EP  - 4405
DO  - 10.1016/j.ceramint.2012.11.029
ER  - 
@article{
author = "Milanović, Igor and Milošević, Sanja S. and Rašković-Lovre, Željka and Novaković, Nikola and Vujasin, Radojka and Matović, Ljiljana and Fernandez, Jose Francisco and Sanchez, Carlos and Grbović-Novaković, Jasmina",
year = "2013",
abstract = "The influence of TiB2 and SiC ceramics on H-desorption kinetics from MgH2 based composites was investigated and correlated with the microstructure and morphology of the composites. The mechanism of desorption and the activation energy for desorption was investigated by applying non-isothermal kinetic analysis of thermodesorption spectra. It has been shown that TiB2 addition leads to significant decrease of the activation energy for desorption, while SiC addition has effect on the interface reaction between hydride and hydroxide. The mechanism of desorption change from Avrami-Erofeev n=3 for pure MgH2 to Avrami Erofeev n=4 for composite materials. The change from 3 to 4 can be due to the modification of the nucleation process or a change in the dimensionality of the growth. Those high values of n discard a diffusion control as a rate limiting step. (C) 2012 Elsevier Ltd and Techna Group S.r.l. All rights reserved.",
journal = "Ceramics International",
title = "Microstructure and hydrogen storage properties of MgH2-TiB2-SiC composites",
volume = "39",
number = "4",
pages = "4399-4405",
doi = "10.1016/j.ceramint.2012.11.029"
}
Milanović, I., Milošević, S. S., Rašković-Lovre, Ž., Novaković, N., Vujasin, R., Matović, L., Fernandez, J. F., Sanchez, C.,& Grbović-Novaković, J.. (2013). Microstructure and hydrogen storage properties of MgH2-TiB2-SiC composites. in Ceramics International, 39(4), 4399-4405.
https://doi.org/10.1016/j.ceramint.2012.11.029
Milanović I, Milošević SS, Rašković-Lovre Ž, Novaković N, Vujasin R, Matović L, Fernandez JF, Sanchez C, Grbović-Novaković J. Microstructure and hydrogen storage properties of MgH2-TiB2-SiC composites. in Ceramics International. 2013;39(4):4399-4405.
doi:10.1016/j.ceramint.2012.11.029 .
Milanović, Igor, Milošević, Sanja S., Rašković-Lovre, Željka, Novaković, Nikola, Vujasin, Radojka, Matović, Ljiljana, Fernandez, Jose Francisco, Sanchez, Carlos, Grbović-Novaković, Jasmina, "Microstructure and hydrogen storage properties of MgH2-TiB2-SiC composites" in Ceramics International, 39, no. 4 (2013):4399-4405,
https://doi.org/10.1016/j.ceramint.2012.11.029 . .
18
18
18

Assessment of changes in desorption mechanism of MgH2 after ion bombardment induced destabilization

Matović, Ljiljana; Kurko, Sandra V.; Rašković-Lovre, Željka; Vujasin, Radojka; Milanović, Igor; Milošević, Sanja S.; Grbović-Novaković, Jasmina

(2012)

TY  - JOUR
AU  - Matović, Ljiljana
AU  - Kurko, Sandra V.
AU  - Rašković-Lovre, Željka
AU  - Vujasin, Radojka
AU  - Milanović, Igor
AU  - Milošević, Sanja S.
AU  - Grbović-Novaković, Jasmina
PY  - 2012
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/4842
AB  - This paper deals with non-isothermal kinetics models of hydrogen desorption from MgH2 altered by ion bombardment and stresses the importance of the MgH2 surface during its decomposition. In the case of argon-irradiated samples, where defects are induced in the near-surface region, the Avrami Erofeev mechanism with parameter n = 2 can be adopted while in the case of boron-irradiated samples, where defects are created deeper in the bulk, the desorption mechanism is the same with n = 3. The difference is possibly related to the concentration and good dispersion of defects in near-surface region in the samples. Copyright (C) 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
T2  - International Journal of Hydrogen Energy
T1  - Assessment of changes in desorption mechanism of MgH2 after ion bombardment induced destabilization
VL  - 37
IS  - 8
SP  - 6727
EP  - 6732
DO  - 10.1016/j.ijhydene.2012.01.084
ER  - 
@article{
author = "Matović, Ljiljana and Kurko, Sandra V. and Rašković-Lovre, Željka and Vujasin, Radojka and Milanović, Igor and Milošević, Sanja S. and Grbović-Novaković, Jasmina",
year = "2012",
abstract = "This paper deals with non-isothermal kinetics models of hydrogen desorption from MgH2 altered by ion bombardment and stresses the importance of the MgH2 surface during its decomposition. In the case of argon-irradiated samples, where defects are induced in the near-surface region, the Avrami Erofeev mechanism with parameter n = 2 can be adopted while in the case of boron-irradiated samples, where defects are created deeper in the bulk, the desorption mechanism is the same with n = 3. The difference is possibly related to the concentration and good dispersion of defects in near-surface region in the samples. Copyright (C) 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.",
journal = "International Journal of Hydrogen Energy",
title = "Assessment of changes in desorption mechanism of MgH2 after ion bombardment induced destabilization",
volume = "37",
number = "8",
pages = "6727-6732",
doi = "10.1016/j.ijhydene.2012.01.084"
}
Matović, L., Kurko, S. V., Rašković-Lovre, Ž., Vujasin, R., Milanović, I., Milošević, S. S.,& Grbović-Novaković, J.. (2012). Assessment of changes in desorption mechanism of MgH2 after ion bombardment induced destabilization. in International Journal of Hydrogen Energy, 37(8), 6727-6732.
https://doi.org/10.1016/j.ijhydene.2012.01.084
Matović L, Kurko SV, Rašković-Lovre Ž, Vujasin R, Milanović I, Milošević SS, Grbović-Novaković J. Assessment of changes in desorption mechanism of MgH2 after ion bombardment induced destabilization. in International Journal of Hydrogen Energy. 2012;37(8):6727-6732.
doi:10.1016/j.ijhydene.2012.01.084 .
Matović, Ljiljana, Kurko, Sandra V., Rašković-Lovre, Željka, Vujasin, Radojka, Milanović, Igor, Milošević, Sanja S., Grbović-Novaković, Jasmina, "Assessment of changes in desorption mechanism of MgH2 after ion bombardment induced destabilization" in International Journal of Hydrogen Energy, 37, no. 8 (2012):6727-6732,
https://doi.org/10.1016/j.ijhydene.2012.01.084 . .
1
14
12
15