Sort By
Publication Year
Deposit Date
Title
Type
Access
Publication Year
2018 (2)
2017 (1)
2016 (2)
2015 (3)
Type

Vasić, Milica M.

Link to this page

Authority KeyName Variants
e4a547d6-27cc-4b2b-8c96-8fbf2dd21f7c
  • Vasić, Milica M. (8)

Author's Bibliography

NiA and NiX zeolites as bifunctional electrocatalysts for water splitting in alkaline media

Milikić, Jadranka; Vasić, Milica M.; Amaral, Luis; Cvjetićanin, Nikola; Jugović, Dragana; Hercigonja, Radmila; Šljukić, Biljana

(Elsevier, 2018)

TY  - JOUR
AU  - Milikić, Jadranka
AU  - Vasić, Milica M.
AU  - Amaral, Luis
AU  - Cvjetićanin, Nikola
AU  - Jugović, Dragana
AU  - Hercigonja, Radmila
AU  - Šljukić, Biljana
PY  - 2018
UR  - http://dais.sanu.ac.rs/123456789/4077
AB  - NiA and NiX zeolites were prepared and characterised using XRD, FTIR and SEM, and subsequently tested as electrodes for hydrogen (HER) and oxygen (OER) evolution reactions in alkaline media. Linear sweep voltammetry and chronoamperometry techniques showed that NiA has higher catalytic activity for these two reactions, as evidenced by higher current densities, which can be correlated with a higher weight fraction of Ni in this electrocatalyst than in the NiX and with its higher conductivity. HER and OER kinetic parameters, including Tafel slope, exchange current density and apparent activation energy were evaluated. Electrochemical impedance spectroscopy analysis yielded values of the resistance of the solution, charge transfer and mass transfer, as well as double layer capacitance and pseudo-capacitance of the working electrode, at different potentials and temperatures. Unlike the HER, during which the mass transfer resistance of the adsorbed intermediate is dominant in the case of NiA, the OER impedance response is controlled by the charge transfer process itself at the potentials of interest for these process. The overall resistance related to the HER is lower for NiA than for NiX. © 2018 Hydrogen Energy Publications LLC
PB  - Elsevier
T2  - International Journal of Hydrogen Energy
T1  - NiA and NiX zeolites as bifunctional electrocatalysts for water splitting in alkaline media
SP  - 18977
EP  - 18991
VL  - 43
IS  - 41
DO  - 10.1016/j.ijhydene.2018.08.063
ER  - 
@article{
author = "Milikić, Jadranka and Vasić, Milica M. and Amaral, Luis and Cvjetićanin, Nikola and Jugović, Dragana and Hercigonja, Radmila and Šljukić, Biljana",
year = "2018",
url = "http://dais.sanu.ac.rs/123456789/4077",
abstract = "NiA and NiX zeolites were prepared and characterised using XRD, FTIR and SEM, and subsequently tested as electrodes for hydrogen (HER) and oxygen (OER) evolution reactions in alkaline media. Linear sweep voltammetry and chronoamperometry techniques showed that NiA has higher catalytic activity for these two reactions, as evidenced by higher current densities, which can be correlated with a higher weight fraction of Ni in this electrocatalyst than in the NiX and with its higher conductivity. HER and OER kinetic parameters, including Tafel slope, exchange current density and apparent activation energy were evaluated. Electrochemical impedance spectroscopy analysis yielded values of the resistance of the solution, charge transfer and mass transfer, as well as double layer capacitance and pseudo-capacitance of the working electrode, at different potentials and temperatures. Unlike the HER, during which the mass transfer resistance of the adsorbed intermediate is dominant in the case of NiA, the OER impedance response is controlled by the charge transfer process itself at the potentials of interest for these process. The overall resistance related to the HER is lower for NiA than for NiX. © 2018 Hydrogen Energy Publications LLC",
publisher = "Elsevier",
journal = "International Journal of Hydrogen Energy",
title = "NiA and NiX zeolites as bifunctional electrocatalysts for water splitting in alkaline media",
pages = "18977-18991",
volume = "43",
number = "41",
doi = "10.1016/j.ijhydene.2018.08.063"
}
Milikić, J., Vasić, M. M., Amaral, L., Cvjetićanin, N., Jugović, D., Hercigonja, R.,& Šljukić, B. (2018). NiA and NiX zeolites as bifunctional electrocatalysts for water splitting in alkaline media.
International Journal of Hydrogen EnergyElsevier., 43(41), 18977-18991.
https://doi.org/10.1016/j.ijhydene.2018.08.063
Milikić J, Vasić MM, Amaral L, Cvjetićanin N, Jugović D, Hercigonja R, Šljukić B. NiA and NiX zeolites as bifunctional electrocatalysts for water splitting in alkaline media. International Journal of Hydrogen Energy. 2018;43(41):18977-18991
Milikić Jadranka, Vasić Milica M., Amaral Luis, Cvjetićanin Nikola, Jugović Dragana, Hercigonja Radmila, Šljukić Biljana, "NiA and NiX zeolites as bifunctional electrocatalysts for water splitting in alkaline media" 43, no. 41 (2018):18977-18991,
https://doi.org/10.1016/j.ijhydene.2018.08.063 .
5
3
5

NiA and NiX zeolites as bifunctional electrocatalysts for water splitting in alkaline media

Milikić, Jadranka; Vasić, Milica M.; Amaral, Luis; Cvjetićanin, Nikola; Jugović, Dragana; Hercigonja, Radmila; Šljukić, Biljana

(Elsevier, 2018)

TY  - JOUR
AU  - Milikić, Jadranka
AU  - Vasić, Milica M.
AU  - Amaral, Luis
AU  - Cvjetićanin, Nikola
AU  - Jugović, Dragana
AU  - Hercigonja, Radmila
AU  - Šljukić, Biljana
PY  - 2018
UR  - http://dais.sanu.ac.rs/123456789/4588
AB  - NiA and NiX zeolites were prepared and characterised using XRD, FTIR and SEM, and subsequently tested as electrodes for hydrogen (HER) and oxygen (OER) evolution reactions in alkaline media. Linear sweep voltammetry and chronoamperometry techniques showed that NiA has higher catalytic activity for these two reactions, as evidenced by higher current densities, which can be correlated with a higher weight fraction of Ni in this electrocatalyst than in the NiX and with its higher conductivity. HER and OER kinetic parameters, including Tafel slope, exchange current density and apparent activation energy were evaluated. Electrochemical impedance spectroscopy analysis yielded values of the resistance of the solution, charge transfer and mass transfer, as well as double layer capacitance and pseudo-capacitance of the working electrode, at different potentials and temperatures. Unlike the HER, during which the mass transfer resistance of the adsorbed intermediate is dominant in the case of NiA, the OER impedance response is controlled by the charge transfer process itself at the potentials of interest for these process. The overall resistance related to the HER is lower for NiA than for NiX. © 2018 Hydrogen Energy Publications LLC
PB  - Elsevier
T2  - International Journal of Hydrogen Energy
T1  - NiA and NiX zeolites as bifunctional electrocatalysts for water splitting in alkaline media
SP  - 18977
EP  - 18991
VL  - 43
IS  - 41
DO  - 10.1016/j.ijhydene.2018.08.063
ER  - 
@article{
author = "Milikić, Jadranka and Vasić, Milica M. and Amaral, Luis and Cvjetićanin, Nikola and Jugović, Dragana and Hercigonja, Radmila and Šljukić, Biljana",
year = "2018",
url = "http://dais.sanu.ac.rs/123456789/4588",
abstract = "NiA and NiX zeolites were prepared and characterised using XRD, FTIR and SEM, and subsequently tested as electrodes for hydrogen (HER) and oxygen (OER) evolution reactions in alkaline media. Linear sweep voltammetry and chronoamperometry techniques showed that NiA has higher catalytic activity for these two reactions, as evidenced by higher current densities, which can be correlated with a higher weight fraction of Ni in this electrocatalyst than in the NiX and with its higher conductivity. HER and OER kinetic parameters, including Tafel slope, exchange current density and apparent activation energy were evaluated. Electrochemical impedance spectroscopy analysis yielded values of the resistance of the solution, charge transfer and mass transfer, as well as double layer capacitance and pseudo-capacitance of the working electrode, at different potentials and temperatures. Unlike the HER, during which the mass transfer resistance of the adsorbed intermediate is dominant in the case of NiA, the OER impedance response is controlled by the charge transfer process itself at the potentials of interest for these process. The overall resistance related to the HER is lower for NiA than for NiX. © 2018 Hydrogen Energy Publications LLC",
publisher = "Elsevier",
journal = "International Journal of Hydrogen Energy",
title = "NiA and NiX zeolites as bifunctional electrocatalysts for water splitting in alkaline media",
pages = "18977-18991",
volume = "43",
number = "41",
doi = "10.1016/j.ijhydene.2018.08.063"
}
Milikić, J., Vasić, M. M., Amaral, L., Cvjetićanin, N., Jugović, D., Hercigonja, R.,& Šljukić, B. (2018). NiA and NiX zeolites as bifunctional electrocatalysts for water splitting in alkaline media.
International Journal of Hydrogen EnergyElsevier., 43(41), 18977-18991.
https://doi.org/10.1016/j.ijhydene.2018.08.063
Milikić J, Vasić MM, Amaral L, Cvjetićanin N, Jugović D, Hercigonja R, Šljukić B. NiA and NiX zeolites as bifunctional electrocatalysts for water splitting in alkaline media. International Journal of Hydrogen Energy. 2018;43(41):18977-18991
Milikić Jadranka, Vasić Milica M., Amaral Luis, Cvjetićanin Nikola, Jugović Dragana, Hercigonja Radmila, Šljukić Biljana, "NiA and NiX zeolites as bifunctional electrocatalysts for water splitting in alkaline media" 43, no. 41 (2018):18977-18991,
https://doi.org/10.1016/j.ijhydene.2018.08.063 .
5
3
5

Synthesis and thermal stability of cis-dichloro[(E)-ethyl-2-(2-((8-hydroxyquinolin-2-il)methylene)hidrazinyl)acetate-κ2 N]-palladium(II) complex

Begović, Nebojša N.; Vasić, Milica M.; Blagojević, Vladimir A.; Filipović, Nenad R.; Marinković, Aleksandar D.; Malešević, Aleksandar; Minić, Dragica M.

(Springer Netherlands, 2017)

TY  - JOUR
AU  - Begović, Nebojša N.
AU  - Vasić, Milica M.
AU  - Blagojević, Vladimir A.
AU  - Filipović, Nenad R.
AU  - Marinković, Aleksandar D.
AU  - Malešević, Aleksandar
AU  - Minić, Dragica M.
PY  - 2017
UR  - http://dais.sanu.ac.rs/123456789/16012
AB  - The structure of new cis-dichloro[(E)-ethyl-2-(2-((8-hydroxyquinolin-2-il)methylene)hidrazinyl)acetate-κ2 N]-palladium(II) complex was determined using a combination of XRD and IR measurements and DFT calculations. Inherent flexibility of its structure is evident from the complexity of its IR spectrum, which could only be theoretically reproduced as a combination of several closely related structures, involving rotation around C–O bond and changes in hydrogen interactions of its –OH group. Its thermal stability and decomposition were studied non-isothermally, and the thermal decomposition mechanism was proposed using correlation with DFT calculations at the molecular level. It was determined that the initial degradation step consists of the release of Cl free radical, which then reacts with both the initial compound and the degradation products. Besides the endothermic steps, there are exothermic ones, contributing to the complex shape of the DSC curve, consisted of overlapping endothermic and exothermic peaks. Deconvolution of DTG curve allowed identification of primary fragments of the initial degradation process and, in conjunction with DFT calculations, construction of the most likely reaction mechanism.
PB  - Springer Netherlands
T2  - Journal of Thermal Analysis and Calorimetry
T1  - Synthesis and thermal stability of cis-dichloro[(E)-ethyl-2-(2-((8-hydroxyquinolin-2-il)methylene)hidrazinyl)acetate-κ2 N]-palladium(II) complex
SP  - 701
EP  - 711
VL  - 130
IS  - 2
DO  - 10.1007/s10973-017-6458-2
ER  - 
@article{
author = "Begović, Nebojša N. and Vasić, Milica M. and Blagojević, Vladimir A. and Filipović, Nenad R. and Marinković, Aleksandar D. and Malešević, Aleksandar and Minić, Dragica M.",
year = "2017",
url = "http://dais.sanu.ac.rs/123456789/16012",
abstract = "The structure of new cis-dichloro[(E)-ethyl-2-(2-((8-hydroxyquinolin-2-il)methylene)hidrazinyl)acetate-κ2 N]-palladium(II) complex was determined using a combination of XRD and IR measurements and DFT calculations. Inherent flexibility of its structure is evident from the complexity of its IR spectrum, which could only be theoretically reproduced as a combination of several closely related structures, involving rotation around C–O bond and changes in hydrogen interactions of its –OH group. Its thermal stability and decomposition were studied non-isothermally, and the thermal decomposition mechanism was proposed using correlation with DFT calculations at the molecular level. It was determined that the initial degradation step consists of the release of Cl free radical, which then reacts with both the initial compound and the degradation products. Besides the endothermic steps, there are exothermic ones, contributing to the complex shape of the DSC curve, consisted of overlapping endothermic and exothermic peaks. Deconvolution of DTG curve allowed identification of primary fragments of the initial degradation process and, in conjunction with DFT calculations, construction of the most likely reaction mechanism.",
publisher = "Springer Netherlands",
journal = "Journal of Thermal Analysis and Calorimetry",
title = "Synthesis and thermal stability of cis-dichloro[(E)-ethyl-2-(2-((8-hydroxyquinolin-2-il)methylene)hidrazinyl)acetate-κ2 N]-palladium(II) complex",
pages = "701-711",
volume = "130",
number = "2",
doi = "10.1007/s10973-017-6458-2"
}
Begović, N. N., Vasić, M. M., Blagojević, V. A., Filipović, N. R., Marinković, A. D., Malešević, A.,& Minić, D. M. (2017). Synthesis and thermal stability of cis-dichloro[(E)-ethyl-2-(2-((8-hydroxyquinolin-2-il)methylene)hidrazinyl)acetate-κ2 N]-palladium(II) complex.
Journal of Thermal Analysis and CalorimetrySpringer Netherlands., 130(2), 701-711.
https://doi.org/10.1007/s10973-017-6458-2
Begović NN, Vasić MM, Blagojević VA, Filipović NR, Marinković AD, Malešević A, Minić DM. Synthesis and thermal stability of cis-dichloro[(E)-ethyl-2-(2-((8-hydroxyquinolin-2-il)methylene)hidrazinyl)acetate-κ2 N]-palladium(II) complex. Journal of Thermal Analysis and Calorimetry. 2017;130(2):701-711
Begović Nebojša N., Vasić Milica M., Blagojević Vladimir A., Filipović Nenad R., Marinković Aleksandar D., Malešević Aleksandar, Minić Dragica M., "Synthesis and thermal stability of cis-dichloro[(E)-ethyl-2-(2-((8-hydroxyquinolin-2-il)methylene)hidrazinyl)acetate-κ2 N]-palladium(II) complex" 130, no. 2 (2017):701-711,
https://doi.org/10.1007/s10973-017-6458-2 .
2
2
2

Thermally Induced Structural Transformations of Fe40Ni40P14B6 Amorphous Alloy

Vasić, Milica M.; Roupcová, Pavla; Pizúrová, Nadežda; Stevanović, Sanja; Blagojević, Vladimir A.; Žák, Tomáš; Minić, Dragica M.

(2016)

TY  - JOUR
AU  - Vasić, Milica M.
AU  - Roupcová, Pavla
AU  - Pizúrová, Nadežda
AU  - Stevanović, Sanja
AU  - Blagojević, Vladimir A.
AU  - Žák, Tomáš
AU  - Minić, Dragica M.
PY  - 2016
UR  - http://dais.sanu.ac.rs/123456789/2327
AB  - Thermal stability and thermally induced structural transformations of Fe40Ni40P14B6 amorphous alloy were examined under non-isothermal and isothermal conditions. Formation of metastable α-(Fe,Ni), and stable γ-(Fe,Ni) and (Fe,Ni)3(P,B) crystalline phases as the main crystallization products was observed, while the presence of small amounts of other crystalline phases like Fe23B6 and Fe2NiB was indicated by electron diffraction in HRTEM. Thermomagnetic curve indicated that Fe content in different crystalline phases is very different, resulting in markedly different Curie temperatures after crystallization. Transmission electron microscopy and atomic force microscopy study suggested multiple-layered platelet-shaped morphology, both on the surface and in the bulk of the crystallized alloy sample. The thermal treatment heating rate and maximum temperature affected surface roughness and grain size inhomogeneity.
T2  - Metallurgical and Materials Transactions A
T1  - Thermally Induced Structural Transformations of Fe40Ni40P14B6 Amorphous Alloy
SP  - 260
EP  - 267
VL  - 47
IS  - 1
DO  - 10.1007/s11661-015-3226-4
ER  - 
@article{
author = "Vasić, Milica M. and Roupcová, Pavla and Pizúrová, Nadežda and Stevanović, Sanja and Blagojević, Vladimir A. and Žák, Tomáš and Minić, Dragica M.",
year = "2016",
url = "http://dais.sanu.ac.rs/123456789/2327",
abstract = "Thermal stability and thermally induced structural transformations of Fe40Ni40P14B6 amorphous alloy were examined under non-isothermal and isothermal conditions. Formation of metastable α-(Fe,Ni), and stable γ-(Fe,Ni) and (Fe,Ni)3(P,B) crystalline phases as the main crystallization products was observed, while the presence of small amounts of other crystalline phases like Fe23B6 and Fe2NiB was indicated by electron diffraction in HRTEM. Thermomagnetic curve indicated that Fe content in different crystalline phases is very different, resulting in markedly different Curie temperatures after crystallization. Transmission electron microscopy and atomic force microscopy study suggested multiple-layered platelet-shaped morphology, both on the surface and in the bulk of the crystallized alloy sample. The thermal treatment heating rate and maximum temperature affected surface roughness and grain size inhomogeneity.",
journal = "Metallurgical and Materials Transactions A",
title = "Thermally Induced Structural Transformations of Fe40Ni40P14B6 Amorphous Alloy",
pages = "260-267",
volume = "47",
number = "1",
doi = "10.1007/s11661-015-3226-4"
}
Vasić, M. M., Roupcová, P., Pizúrová, N., Stevanović, S., Blagojević, V. A., Žák, T.,& Minić, D. M. (2016). Thermally Induced Structural Transformations of Fe40Ni40P14B6 Amorphous Alloy.
Metallurgical and Materials Transactions A, 47(1), 260-267.
https://doi.org/10.1007/s11661-015-3226-4
Vasić MM, Roupcová P, Pizúrová N, Stevanović S, Blagojević VA, Žák T, Minić DM. Thermally Induced Structural Transformations of Fe40Ni40P14B6 Amorphous Alloy. Metallurgical and Materials Transactions A. 2016;47(1):260-267
Vasić Milica M., Roupcová Pavla, Pizúrová Nadežda, Stevanović Sanja, Blagojević Vladimir A., Žák Tomáš, Minić Dragica M., "Thermally Induced Structural Transformations of Fe40Ni40P14B6 Amorphous Alloy" 47, no. 1 (2016):260-267,
https://doi.org/10.1007/s11661-015-3226-4 .
2
2

Thermal stability and degradation of binuclear hexaaqua-bis(ethylenediamine)-(μ 2-pyromellitato)dinickel(II) tetrahydrate

Zdravković, Jelena D.; Poleti, Dejan; Rogan, Jelena; Begović, Nebojša N.; Blagojević, Vladimir A.; Vasić, Milica M.; Minić, Dragica M.

(Springer, 2016)

TY  - JOUR
AU  - Zdravković, Jelena D.
AU  - Poleti, Dejan
AU  - Rogan, Jelena
AU  - Begović, Nebojša N.
AU  - Blagojević, Vladimir A.
AU  - Vasić, Milica M.
AU  - Minić, Dragica M.
PY  - 2016
UR  - http://dais.sanu.ac.rs/123456789/16009
AB  - Thermal degradation of ternary transition metal complex containing tetraanion of pyromellitic acid, pyr, and ethylenediamine, en, [Ni2(en)2(H2O)6(pyr)]·4H2O, 1, was investigated under non-isothermal conditions. The mechanism of thermal degradation, which occurs in three steps, was clarified by TG/DSC measurements in conjunction with FT-IR spectroscopy and XRPD analysis. The complexity of all degradation steps has been revealed using isoconversional methods. Dehydration comprises the loss of ten water molecules in a relatively narrow temperature interval, resulting in a very complicated reaction mechanism. In addition, density functional theory calculations have been applied for better understanding of dehydration. The second degradation step, related to loss of en, was separated into two single-step processes with Fraser–Suzuki function. The obtained individual steps were described by Johnson–Mehl–Avrami A2 model and Šesták–Berggren model, respectively. Validation of the proposed kinetic triplets for individual steps was performed using master plot and Pérez-Maqueda criteria. The third degradation step is related to the fragmentation of pyr ion most likely followed with the release of a number of gaseous products.
PB  - Springer
T2  - Journal of Thermal Analysis and Calorimetry
T1  - Thermal stability and degradation of binuclear hexaaqua-bis(ethylenediamine)-(μ 2-pyromellitato)dinickel(II) tetrahydrate
SP  - 1715
EP  - 1726
VL  - 123
IS  - 2
DO  - 10.1007/s10973-015-5007-0
ER  - 
@article{
author = "Zdravković, Jelena D. and Poleti, Dejan and Rogan, Jelena and Begović, Nebojša N. and Blagojević, Vladimir A. and Vasić, Milica M. and Minić, Dragica M.",
year = "2016",
url = "http://dais.sanu.ac.rs/123456789/16009",
abstract = "Thermal degradation of ternary transition metal complex containing tetraanion of pyromellitic acid, pyr, and ethylenediamine, en, [Ni2(en)2(H2O)6(pyr)]·4H2O, 1, was investigated under non-isothermal conditions. The mechanism of thermal degradation, which occurs in three steps, was clarified by TG/DSC measurements in conjunction with FT-IR spectroscopy and XRPD analysis. The complexity of all degradation steps has been revealed using isoconversional methods. Dehydration comprises the loss of ten water molecules in a relatively narrow temperature interval, resulting in a very complicated reaction mechanism. In addition, density functional theory calculations have been applied for better understanding of dehydration. The second degradation step, related to loss of en, was separated into two single-step processes with Fraser–Suzuki function. The obtained individual steps were described by Johnson–Mehl–Avrami A2 model and Šesták–Berggren model, respectively. Validation of the proposed kinetic triplets for individual steps was performed using master plot and Pérez-Maqueda criteria. The third degradation step is related to the fragmentation of pyr ion most likely followed with the release of a number of gaseous products.",
publisher = "Springer",
journal = "Journal of Thermal Analysis and Calorimetry",
title = "Thermal stability and degradation of binuclear hexaaqua-bis(ethylenediamine)-(μ 2-pyromellitato)dinickel(II) tetrahydrate",
pages = "1715-1726",
volume = "123",
number = "2",
doi = "10.1007/s10973-015-5007-0"
}
Zdravković, J. D., Poleti, D., Rogan, J., Begović, N. N., Blagojević, V. A., Vasić, M. M.,& Minić, D. M. (2016). Thermal stability and degradation of binuclear hexaaqua-bis(ethylenediamine)-(μ 2-pyromellitato)dinickel(II) tetrahydrate.
Journal of Thermal Analysis and CalorimetrySpringer., 123(2), 1715-1726.
https://doi.org/10.1007/s10973-015-5007-0
Zdravković JD, Poleti D, Rogan J, Begović NN, Blagojević VA, Vasić MM, Minić DM. Thermal stability and degradation of binuclear hexaaqua-bis(ethylenediamine)-(μ 2-pyromellitato)dinickel(II) tetrahydrate. Journal of Thermal Analysis and Calorimetry. 2016;123(2):1715-1726
Zdravković Jelena D., Poleti Dejan, Rogan Jelena, Begović Nebojša N., Blagojević Vladimir A., Vasić Milica M., Minić Dragica M., "Thermal stability and degradation of binuclear hexaaqua-bis(ethylenediamine)-(μ 2-pyromellitato)dinickel(II) tetrahydrate" 123, no. 2 (2016):1715-1726,
https://doi.org/10.1007/s10973-015-5007-0 .
3
4
4

Thermal stability and mechanism of thermally induced crystallization of Fe73.5Cu1Nb3Si15.5B7 amorphous alloy

Vasić, Milica M.; Minić, Dragica M.; Blagojević, Vladimir A.; Žák, Tomáš; Pizúrová, Nadežda; David, B.; Minić, Dragica

(Warsaw : Polish Academy of Sciences, Institute of Physics, 2015)

TY  - JOUR
AU  - Vasić, Milica M.
AU  - Minić, Dragica M.
AU  - Blagojević, Vladimir A.
AU  - Žák, Tomáš
AU  - Pizúrová, Nadežda
AU  - David, B.
AU  - Minić, Dragica
PY  - 2015
UR  - http://dais.sanu.ac.rs/123456789/3518
AB  - Investigation of thermal stability of the alloy revealed stepwise crystallization process, manifested by two distinct complex exothermic peaks in differential scanning calorimetry curves. Kinetic parameters of individual crystallization steps were found using the Kissinger and Vyazovkin methods. Structural characterization of thermally treated samples showed formation of different iron-based phases including α-Fe(Si), Fe2B, Fe16Nb6Si7 and Fe2Si and some metastable intermediary species. Morphology characterization of the surface and cross-section of the thermally treated samples showed granulated structure composed of several different phases and indicated occurrence of impingement effects during crystal growth. Value of estimated lifetime suggested very high stability against crystallization at room temperature and abrupt decrease of lifetime with temperature increase.
PB  - Warsaw : Polish Academy of Sciences, Institute of Physics
T2  - Acta Physica Polonica A
T1  - Thermal stability and mechanism of thermally induced crystallization of Fe73.5Cu1Nb3Si15.5B7 amorphous alloy
SP  - 657
EP  - 660
VL  - 128
IS  - 4
DO  - 10.12693/APhysPolA.128.657
ER  - 
@article{
author = "Vasić, Milica M. and Minić, Dragica M. and Blagojević, Vladimir A. and Žák, Tomáš and Pizúrová, Nadežda and David, B. and Minić, Dragica",
year = "2015",
url = "http://dais.sanu.ac.rs/123456789/3518",
abstract = "Investigation of thermal stability of the alloy revealed stepwise crystallization process, manifested by two distinct complex exothermic peaks in differential scanning calorimetry curves. Kinetic parameters of individual crystallization steps were found using the Kissinger and Vyazovkin methods. Structural characterization of thermally treated samples showed formation of different iron-based phases including α-Fe(Si), Fe2B, Fe16Nb6Si7 and Fe2Si and some metastable intermediary species. Morphology characterization of the surface and cross-section of the thermally treated samples showed granulated structure composed of several different phases and indicated occurrence of impingement effects during crystal growth. Value of estimated lifetime suggested very high stability against crystallization at room temperature and abrupt decrease of lifetime with temperature increase.",
publisher = "Warsaw : Polish Academy of Sciences, Institute of Physics",
journal = "Acta Physica Polonica A",
title = "Thermal stability and mechanism of thermally induced crystallization of Fe73.5Cu1Nb3Si15.5B7 amorphous alloy",
pages = "657-660",
volume = "128",
number = "4",
doi = "10.12693/APhysPolA.128.657"
}
Vasić, M. M., Minić, D. M., Blagojević, V. A., Žák, T., Pizúrová, N., David, B.,& Minić, D. (2015). Thermal stability and mechanism of thermally induced crystallization of Fe73.5Cu1Nb3Si15.5B7 amorphous alloy.
Acta Physica Polonica AWarsaw : Polish Academy of Sciences, Institute of Physics., 128(4), 657-660.
https://doi.org/10.12693/APhysPolA.128.657
Vasić MM, Minić DM, Blagojević VA, Žák T, Pizúrová N, David B, Minić D. Thermal stability and mechanism of thermally induced crystallization of Fe73.5Cu1Nb3Si15.5B7 amorphous alloy. Acta Physica Polonica A. 2015;128(4):657-660
Vasić Milica M., Minić Dragica M., Blagojević Vladimir A., Žák Tomáš, Pizúrová Nadežda, David B., Minić Dragica, "Thermal stability and mechanism of thermally induced crystallization of Fe73.5Cu1Nb3Si15.5B7 amorphous alloy" 128, no. 4 (2015):657-660,
https://doi.org/10.12693/APhysPolA.128.657 .
2
1
1

Thermally induced crystallization of amorphous Fe40Ni40P14B6 alloy

Vasić, Milica M.; Blagojević, Vladimir A.; Begović, Nebojša N.; Žák, Tomáš; Pavlović, Vladimir B.; Minić, Dragica M.

(Elsevier, 2015)

TY  - JOUR
AU  - Vasić, Milica M.
AU  - Blagojević, Vladimir A.
AU  - Begović, Nebojša N.
AU  - Žák, Tomáš
AU  - Pavlović, Vladimir B.
AU  - Minić, Dragica M.
PY  - 2015
UR  - http://dais.sanu.ac.rs/123456789/3522
AB  - The crystallization mechanism and kinetics of Fe40Ni40P14B6 amorphous alloy were studied under non-isothermal conditions. Thermal stabilization of this alloy manifests in DSC through two complex peaks, corresponding to crystallization and recrystallization, respectively. The complex crystallization DSC peak was deconvoluted into individual steps corresponding to crystallization of individual phases, where the results using both Gaussian-Lorentzian cross-product and Fraser-Suzuki function were compared. It was determined that the values of kinetic triplets of the individual steps did not exhibit any significant difference, depending on the deconvolution function. Anisotropic growth was indicated to be the prevailing type of impingement for all crystallization steps. Using the calculated values of the respective kinetic triplets and the mechanisms determined from the value of Avrami exponent, distinct values of activation energies for nucleation and crystal growth for crystallization of each individual phase were calculated, showing significantly higher values for nucleation than those for crystal growth. Alloy samples treated non-isothermally in the DSC cell exhibit inhomogeneous surface morphology with highly granulated structure dependent on heating rate. © 2015 Elsevier B.V. All rights reserved.
PB  - Elsevier
T2  - Thermochimica Acta
T1  - Thermally induced crystallization of amorphous Fe40Ni40P14B6 alloy
SP  - 129
EP  - 136
VL  - 614
DO  - 10.1016/j.tca.2015.06.015
ER  - 
@article{
author = "Vasić, Milica M. and Blagojević, Vladimir A. and Begović, Nebojša N. and Žák, Tomáš and Pavlović, Vladimir B. and Minić, Dragica M.",
year = "2015",
url = "http://dais.sanu.ac.rs/123456789/3522",
abstract = "The crystallization mechanism and kinetics of Fe40Ni40P14B6 amorphous alloy were studied under non-isothermal conditions. Thermal stabilization of this alloy manifests in DSC through two complex peaks, corresponding to crystallization and recrystallization, respectively. The complex crystallization DSC peak was deconvoluted into individual steps corresponding to crystallization of individual phases, where the results using both Gaussian-Lorentzian cross-product and Fraser-Suzuki function were compared. It was determined that the values of kinetic triplets of the individual steps did not exhibit any significant difference, depending on the deconvolution function. Anisotropic growth was indicated to be the prevailing type of impingement for all crystallization steps. Using the calculated values of the respective kinetic triplets and the mechanisms determined from the value of Avrami exponent, distinct values of activation energies for nucleation and crystal growth for crystallization of each individual phase were calculated, showing significantly higher values for nucleation than those for crystal growth. Alloy samples treated non-isothermally in the DSC cell exhibit inhomogeneous surface morphology with highly granulated structure dependent on heating rate. © 2015 Elsevier B.V. All rights reserved.",
publisher = "Elsevier",
journal = "Thermochimica Acta",
title = "Thermally induced crystallization of amorphous Fe40Ni40P14B6 alloy",
pages = "129-136",
volume = "614",
doi = "10.1016/j.tca.2015.06.015"
}
Vasić, M. M., Blagojević, V. A., Begović, N. N., Žák, T., Pavlović, V. B.,& Minić, D. M. (2015). Thermally induced crystallization of amorphous Fe40Ni40P14B6 alloy.
Thermochimica ActaElsevier., 614, 129-136.
https://doi.org/10.1016/j.tca.2015.06.015
Vasić MM, Blagojević VA, Begović NN, Žák T, Pavlović VB, Minić DM. Thermally induced crystallization of amorphous Fe40Ni40P14B6 alloy. Thermochimica Acta. 2015;614:129-136
Vasić Milica M., Blagojević Vladimir A., Begović Nebojša N., Žák Tomáš, Pavlović Vladimir B., Minić Dragica M., "Thermally induced crystallization of amorphous Fe40Ni40P14B6 alloy" 614 (2015):129-136,
https://doi.org/10.1016/j.tca.2015.06.015 .
10
5
7

Thermally induced crystallization of amorphous Fe40Ni40P14B6 alloy

Vasić, Milica M.; Blagojević, Vladimir A.; Begović, Nebojša N.; Žák, Tomáš; Pavlović, Vladimir B.; Minić, Dragica M.

(Elsevier, 2015)

TY  - JOUR
AU  - Vasić, Milica M.
AU  - Blagojević, Vladimir A.
AU  - Begović, Nebojša N.
AU  - Žák, Tomáš
AU  - Pavlović, Vladimir B.
AU  - Minić, Dragica M.
PY  - 2015
UR  - http://dais.sanu.ac.rs/123456789/4674
AB  - The crystallization mechanism and kinetics of Fe40Ni40P14B6 amorphous alloy were studied under non-isothermal conditions. Thermal stabilization of this alloy manifests in DSC through two complex peaks, corresponding to crystallization and recrystallization, respectively. The complex crystallization DSC peak was deconvoluted into individual steps corresponding to crystallization of individual phases, where the results using both Gaussian-Lorentzian cross-product and Fraser-Suzuki function were compared. It was determined that the values of kinetic triplets of the individual steps did not exhibit any significant difference, depending on the deconvolution function. Anisotropic growth was indicated to be the prevailing type of impingement for all crystallization steps. Using the calculated values of the respective kinetic triplets and the mechanisms determined from the value of Avrami exponent, distinct values of activation energies for nucleation and crystal growth for crystallization of each individual phase were calculated, showing significantly higher values for nucleation than those for crystal growth. Alloy samples treated non-isothermally in the DSC cell exhibit inhomogeneous surface morphology with highly granulated structure dependent on heating rate. © 2015 Elsevier B.V. All rights reserved.
PB  - Elsevier
T2  - Thermochimica Acta
T1  - Thermally induced crystallization of amorphous Fe40Ni40P14B6 alloy
SP  - 129
EP  - 136
VL  - 614
DO  - 10.1016/j.tca.2015.06.015
ER  - 
@article{
author = "Vasić, Milica M. and Blagojević, Vladimir A. and Begović, Nebojša N. and Žák, Tomáš and Pavlović, Vladimir B. and Minić, Dragica M.",
year = "2015",
url = "http://dais.sanu.ac.rs/123456789/4674",
abstract = "The crystallization mechanism and kinetics of Fe40Ni40P14B6 amorphous alloy were studied under non-isothermal conditions. Thermal stabilization of this alloy manifests in DSC through two complex peaks, corresponding to crystallization and recrystallization, respectively. The complex crystallization DSC peak was deconvoluted into individual steps corresponding to crystallization of individual phases, where the results using both Gaussian-Lorentzian cross-product and Fraser-Suzuki function were compared. It was determined that the values of kinetic triplets of the individual steps did not exhibit any significant difference, depending on the deconvolution function. Anisotropic growth was indicated to be the prevailing type of impingement for all crystallization steps. Using the calculated values of the respective kinetic triplets and the mechanisms determined from the value of Avrami exponent, distinct values of activation energies for nucleation and crystal growth for crystallization of each individual phase were calculated, showing significantly higher values for nucleation than those for crystal growth. Alloy samples treated non-isothermally in the DSC cell exhibit inhomogeneous surface morphology with highly granulated structure dependent on heating rate. © 2015 Elsevier B.V. All rights reserved.",
publisher = "Elsevier",
journal = "Thermochimica Acta",
title = "Thermally induced crystallization of amorphous Fe40Ni40P14B6 alloy",
pages = "129-136",
volume = "614",
doi = "10.1016/j.tca.2015.06.015"
}
Vasić, M. M., Blagojević, V. A., Begović, N. N., Žák, T., Pavlović, V. B.,& Minić, D. M. (2015). Thermally induced crystallization of amorphous Fe40Ni40P14B6 alloy.
Thermochimica ActaElsevier., 614, 129-136.
https://doi.org/10.1016/j.tca.2015.06.015
Vasić MM, Blagojević VA, Begović NN, Žák T, Pavlović VB, Minić DM. Thermally induced crystallization of amorphous Fe40Ni40P14B6 alloy. Thermochimica Acta. 2015;614:129-136
Vasić Milica M., Blagojević Vladimir A., Begović Nebojša N., Žák Tomáš, Pavlović Vladimir B., Minić Dragica M., "Thermally induced crystallization of amorphous Fe40Ni40P14B6 alloy" 614 (2015):129-136,
https://doi.org/10.1016/j.tca.2015.06.015 .
10
5
8