Poleti, Dejan

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orcid::0000-0001-8162-1017
  • Poleti, Dejan (13)
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Author's Bibliography

The influence of alkaline cations on the mechanism and kinetics of dehydration of polymeric phthalatocuprate(II) dihydrates

Zdravković, Jelena D.; Poleti, Dejan; Rogan, Jelena; Blagojević, Vladimir A.; Mészáros, Katalin; Minić, Dragica M.

(Elsevier, 2017)

TY  - JOUR
AU  - Zdravković, Jelena D.
AU  - Poleti, Dejan
AU  - Rogan, Jelena
AU  - Blagojević, Vladimir A.
AU  - Mészáros, Katalin
AU  - Minić, Dragica M.
PY  - 2017
UR  - http://dais.sanu.ac.rs/123456789/4616
AB  - Thermal dehydration of two heterometallic complexes containing dianion of phthalic acid, pht, Na2[Cu(pht)2] · 2H2O, 1, and K2[Cu(pht)2] · 2H2O, 2, was investigated under non-isothermal conditions. Mechanism and kinetics of dehydration were analyzed in detail using TG/DSC/MS measurements, XRPD analysis and FT-IR spectroscopy. The reversibility of dehydration processes was identified. According to XRPD, dehydrated product of 1 maintains original structure, but dehydration of 2 undergoes structural transformation giving a dehydrated product of different crystal structure. In both cases dehydration process involves more than one elementary step, which was confirmed using isoconversional methods Deconvolution of this process using Fraiser-Suzuki function yielded two single step processes for 1 and 2. Subsequent kinetic analysis was performed using Màlek algorithm, resulting in the determination of kinetic triplets (Ea, A and f(α)) for each individual step. In addition, the dehydrated complexes were investigated as possible candidates for H2 adsorption, using molecular simulations.
PB  - Elsevier
T2  - Journal of Analytical and Applied Pyrolysis
T1  - The influence of alkaline cations on the mechanism and kinetics of dehydration of polymeric phthalatocuprate(II) dihydrates
SP  - 323
EP  - 331
VL  - 126
DO  - 10.1016/j.jaap.2017.05.014
UR  - https://hdl.handle.net/21.15107/rcub_dais_4616
ER  - 
@article{
author = "Zdravković, Jelena D. and Poleti, Dejan and Rogan, Jelena and Blagojević, Vladimir A. and Mészáros, Katalin and Minić, Dragica M.",
year = "2017",
abstract = "Thermal dehydration of two heterometallic complexes containing dianion of phthalic acid, pht, Na2[Cu(pht)2] · 2H2O, 1, and K2[Cu(pht)2] · 2H2O, 2, was investigated under non-isothermal conditions. Mechanism and kinetics of dehydration were analyzed in detail using TG/DSC/MS measurements, XRPD analysis and FT-IR spectroscopy. The reversibility of dehydration processes was identified. According to XRPD, dehydrated product of 1 maintains original structure, but dehydration of 2 undergoes structural transformation giving a dehydrated product of different crystal structure. In both cases dehydration process involves more than one elementary step, which was confirmed using isoconversional methods Deconvolution of this process using Fraiser-Suzuki function yielded two single step processes for 1 and 2. Subsequent kinetic analysis was performed using Màlek algorithm, resulting in the determination of kinetic triplets (Ea, A and f(α)) for each individual step. In addition, the dehydrated complexes were investigated as possible candidates for H2 adsorption, using molecular simulations.",
publisher = "Elsevier",
journal = "Journal of Analytical and Applied Pyrolysis",
title = "The influence of alkaline cations on the mechanism and kinetics of dehydration of polymeric phthalatocuprate(II) dihydrates",
pages = "323-331",
volume = "126",
doi = "10.1016/j.jaap.2017.05.014",
url = "https://hdl.handle.net/21.15107/rcub_dais_4616"
}
Zdravković, J. D., Poleti, D., Rogan, J., Blagojević, V. A., Mészáros, K.,& Minić, D. M.. (2017). The influence of alkaline cations on the mechanism and kinetics of dehydration of polymeric phthalatocuprate(II) dihydrates. in Journal of Analytical and Applied Pyrolysis
Elsevier., 126, 323-331.
https://doi.org/10.1016/j.jaap.2017.05.014
https://hdl.handle.net/21.15107/rcub_dais_4616
Zdravković JD, Poleti D, Rogan J, Blagojević VA, Mészáros K, Minić DM. The influence of alkaline cations on the mechanism and kinetics of dehydration of polymeric phthalatocuprate(II) dihydrates. in Journal of Analytical and Applied Pyrolysis. 2017;126:323-331.
doi:10.1016/j.jaap.2017.05.014
https://hdl.handle.net/21.15107/rcub_dais_4616 .
Zdravković, Jelena D., Poleti, Dejan, Rogan, Jelena, Blagojević, Vladimir A., Mészáros, Katalin, Minić, Dragica M., "The influence of alkaline cations on the mechanism and kinetics of dehydration of polymeric phthalatocuprate(II) dihydrates" in Journal of Analytical and Applied Pyrolysis, 126 (2017):323-331,
https://doi.org/10.1016/j.jaap.2017.05.014 .,
https://hdl.handle.net/21.15107/rcub_dais_4616 .
1
1
1

The influence of alkaline cations on the mechanism and kinetics of dehydration of polymeric phthalatocuprate(II) dihydrates

Zdravković, Jelena D.; Poleti, Dejan; Rogan, Jelena; Blagojević, Vladimir A.; Mészáros, Katalin; Minić, Dragica M.

(Elsevier, 2017)

TY  - JOUR
AU  - Zdravković, Jelena D.
AU  - Poleti, Dejan
AU  - Rogan, Jelena
AU  - Blagojević, Vladimir A.
AU  - Mészáros, Katalin
AU  - Minić, Dragica M.
PY  - 2017
UR  - http://dais.sanu.ac.rs/123456789/2351
AB  - Thermal dehydration of two heterometallic complexes containing dianion of phthalic acid, pht, Na2[Cu(pht)2] · 2H2O, 1, and K2[Cu(pht)2] · 2H2O, 2, was investigated under non-isothermal conditions. Mechanism and kinetics of dehydration were analyzed in detail using TG/DSC/MS measurements, XRPD analysis and FT-IR spectroscopy. The reversibility of dehydration processes was identified. According to XRPD, dehydrated product of 1 maintains original structure, but dehydration of 2 undergoes structural transformation giving a dehydrated product of different crystal structure. In both cases dehydration process involves more than one elementary step, which was confirmed using isoconversional methods Deconvolution of this process using Fraiser-Suzuki function yielded two single step processes for 1 and 2. Subsequent kinetic analysis was performed using Màlek algorithm, resulting in the determination of kinetic triplets (Ea, A and f(α)) for each individual step. In addition, the dehydrated complexes were investigated as possible candidates for H2 adsorption, using molecular simulations.
PB  - Elsevier
T2  - Journal of Analytical and Applied Pyrolysis
T1  - The influence of alkaline cations on the mechanism and kinetics of dehydration of polymeric phthalatocuprate(II) dihydrates
SP  - 323
EP  - 331
VL  - 126
DO  - 10.1016/j.jaap.2017.05.014
UR  - https://hdl.handle.net/21.15107/rcub_dais_2351
ER  - 
@article{
author = "Zdravković, Jelena D. and Poleti, Dejan and Rogan, Jelena and Blagojević, Vladimir A. and Mészáros, Katalin and Minić, Dragica M.",
year = "2017",
abstract = "Thermal dehydration of two heterometallic complexes containing dianion of phthalic acid, pht, Na2[Cu(pht)2] · 2H2O, 1, and K2[Cu(pht)2] · 2H2O, 2, was investigated under non-isothermal conditions. Mechanism and kinetics of dehydration were analyzed in detail using TG/DSC/MS measurements, XRPD analysis and FT-IR spectroscopy. The reversibility of dehydration processes was identified. According to XRPD, dehydrated product of 1 maintains original structure, but dehydration of 2 undergoes structural transformation giving a dehydrated product of different crystal structure. In both cases dehydration process involves more than one elementary step, which was confirmed using isoconversional methods Deconvolution of this process using Fraiser-Suzuki function yielded two single step processes for 1 and 2. Subsequent kinetic analysis was performed using Màlek algorithm, resulting in the determination of kinetic triplets (Ea, A and f(α)) for each individual step. In addition, the dehydrated complexes were investigated as possible candidates for H2 adsorption, using molecular simulations.",
publisher = "Elsevier",
journal = "Journal of Analytical and Applied Pyrolysis",
title = "The influence of alkaline cations on the mechanism and kinetics of dehydration of polymeric phthalatocuprate(II) dihydrates",
pages = "323-331",
volume = "126",
doi = "10.1016/j.jaap.2017.05.014",
url = "https://hdl.handle.net/21.15107/rcub_dais_2351"
}
Zdravković, J. D., Poleti, D., Rogan, J., Blagojević, V. A., Mészáros, K.,& Minić, D. M.. (2017). The influence of alkaline cations on the mechanism and kinetics of dehydration of polymeric phthalatocuprate(II) dihydrates. in Journal of Analytical and Applied Pyrolysis
Elsevier., 126, 323-331.
https://doi.org/10.1016/j.jaap.2017.05.014
https://hdl.handle.net/21.15107/rcub_dais_2351
Zdravković JD, Poleti D, Rogan J, Blagojević VA, Mészáros K, Minić DM. The influence of alkaline cations on the mechanism and kinetics of dehydration of polymeric phthalatocuprate(II) dihydrates. in Journal of Analytical and Applied Pyrolysis. 2017;126:323-331.
doi:10.1016/j.jaap.2017.05.014
https://hdl.handle.net/21.15107/rcub_dais_2351 .
Zdravković, Jelena D., Poleti, Dejan, Rogan, Jelena, Blagojević, Vladimir A., Mészáros, Katalin, Minić, Dragica M., "The influence of alkaline cations on the mechanism and kinetics of dehydration of polymeric phthalatocuprate(II) dihydrates" in Journal of Analytical and Applied Pyrolysis, 126 (2017):323-331,
https://doi.org/10.1016/j.jaap.2017.05.014 .,
https://hdl.handle.net/21.15107/rcub_dais_2351 .
1
1
1

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
UR  - https://hdl.handle.net/21.15107/rcub_dais_16009
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",
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",
url = "https://hdl.handle.net/21.15107/rcub_dais_16009"
}
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. in Journal of Thermal Analysis and Calorimetry
Springer., 123(2), 1715-1726.
https://doi.org/10.1007/s10973-015-5007-0
https://hdl.handle.net/21.15107/rcub_dais_16009
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. in Journal of Thermal Analysis and Calorimetry. 2016;123(2):1715-1726.
doi:10.1007/s10973-015-5007-0
https://hdl.handle.net/21.15107/rcub_dais_16009 .
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" in Journal of Thermal Analysis and Calorimetry, 123, no. 2 (2016):1715-1726,
https://doi.org/10.1007/s10973-015-5007-0 .,
https://hdl.handle.net/21.15107/rcub_dais_16009 .
3
4
4

Ni-(Ebonex-supported Ir) composite coatings as electrocatalysts for alkaline water electrolysis. Part II: Oxygen evolution

Jović, Borka; Lačnjevac, Uroš; Jović, Vladimir; Gajić Krstajić, Ljiljana; Kovač, Janez; Poleti, Dejan; Krstajić, Nedeljko

(2016)

TY  - JOUR
AU  - Jović, Borka
AU  - Lačnjevac, Uroš
AU  - Jović, Vladimir
AU  - Gajić Krstajić, Ljiljana
AU  - Kovač, Janez
AU  - Poleti, Dejan
AU  - Krstajić, Nedeljko
PY  - 2016
UR  - http://dais.sanu.ac.rs/123456789/15978
AB  - The oxygen evolution reaction (OER) was studied at pure Ni and Ni-(Ebonex/Ir) composite coatings in 1 M NaOH solution at 25 °C. Ni-(Ebonex-supported Ir) coatings were electrodeposited from a nickel Watts bath containing different concentrations of suspended Ebonex/Ir particles (0–2 g dm−3) onto a Ni 40 mesh substrate. The surface morphology of the coatings was examined by scanning electron microscopy (SEM), the surface composition by energy dispersive X-ray spectroscopy (EDS), X-ray powder diffraction (XRPD) and X-ray photoelectron spectroscopy (XPS), whereas the electrochemical properties were studied by electrochemical impedance spectroscopy (EIS), polarization measurements and cyclic voltammetry (CV). It was shown that the roughness factor of Ni-(Ebonex/Ir) composite coatings calculated relative to the surface area of the pure Ni sample increased with the increasing content of Ebonex/Ir particles in the bath to a maximum value of 40.6. All samples displayed a Tafel slope of about 60 mV dec−1 in the potential range corresponding to lower current densities for the OER. The increase of the apparent activity for the OER at Ni-(Ebonex/Ir) coatings compared with the pure Ni coating was attributed only to the increase of the electrochemically active surface area. Although the pure Ni coating initially exhibited higher intrinsic catalytic activity for the OER than the composite coatings, it also showed a drastic loss of activity after subjecting to continuous oxygen evolution at j = 50 mA cm−2 for 24 h (ΔE = 395 mV). At the same time, the OER overpotential at Ni-(Ebonex/Ir) coatings only negligibly increased after the stability test (ΔE = 22 mV). The improved retention of catalytic activity observed with Ni-(Ebonex/Ir) coatings was ascribed to the presence of IrO2, which inhibited the formation of the inactive γ-NiOOH phase.
T2  - International Journal of Hydrogen Energy
T1  - Ni-(Ebonex-supported Ir) composite coatings as electrocatalysts for alkaline water electrolysis. Part II: Oxygen evolution
SP  - 20502
EP  - 20514
VL  - 41
IS  - 45
DO  - 10.1016/j.ijhydene.2016.08.226
UR  - https://hdl.handle.net/21.15107/rcub_dais_15978
ER  - 
@article{
author = "Jović, Borka and Lačnjevac, Uroš and Jović, Vladimir and Gajić Krstajić, Ljiljana and Kovač, Janez and Poleti, Dejan and Krstajić, Nedeljko",
year = "2016",
abstract = "The oxygen evolution reaction (OER) was studied at pure Ni and Ni-(Ebonex/Ir) composite coatings in 1 M NaOH solution at 25 °C. Ni-(Ebonex-supported Ir) coatings were electrodeposited from a nickel Watts bath containing different concentrations of suspended Ebonex/Ir particles (0–2 g dm−3) onto a Ni 40 mesh substrate. The surface morphology of the coatings was examined by scanning electron microscopy (SEM), the surface composition by energy dispersive X-ray spectroscopy (EDS), X-ray powder diffraction (XRPD) and X-ray photoelectron spectroscopy (XPS), whereas the electrochemical properties were studied by electrochemical impedance spectroscopy (EIS), polarization measurements and cyclic voltammetry (CV). It was shown that the roughness factor of Ni-(Ebonex/Ir) composite coatings calculated relative to the surface area of the pure Ni sample increased with the increasing content of Ebonex/Ir particles in the bath to a maximum value of 40.6. All samples displayed a Tafel slope of about 60 mV dec−1 in the potential range corresponding to lower current densities for the OER. The increase of the apparent activity for the OER at Ni-(Ebonex/Ir) coatings compared with the pure Ni coating was attributed only to the increase of the electrochemically active surface area. Although the pure Ni coating initially exhibited higher intrinsic catalytic activity for the OER than the composite coatings, it also showed a drastic loss of activity after subjecting to continuous oxygen evolution at j = 50 mA cm−2 for 24 h (ΔE = 395 mV). At the same time, the OER overpotential at Ni-(Ebonex/Ir) coatings only negligibly increased after the stability test (ΔE = 22 mV). The improved retention of catalytic activity observed with Ni-(Ebonex/Ir) coatings was ascribed to the presence of IrO2, which inhibited the formation of the inactive γ-NiOOH phase.",
journal = "International Journal of Hydrogen Energy",
title = "Ni-(Ebonex-supported Ir) composite coatings as electrocatalysts for alkaline water electrolysis. Part II: Oxygen evolution",
pages = "20502-20514",
volume = "41",
number = "45",
doi = "10.1016/j.ijhydene.2016.08.226",
url = "https://hdl.handle.net/21.15107/rcub_dais_15978"
}
Jović, B., Lačnjevac, U., Jović, V., Gajić Krstajić, L., Kovač, J., Poleti, D.,& Krstajić, N.. (2016). Ni-(Ebonex-supported Ir) composite coatings as electrocatalysts for alkaline water electrolysis. Part II: Oxygen evolution. in International Journal of Hydrogen Energy, 41(45), 20502-20514.
https://doi.org/10.1016/j.ijhydene.2016.08.226
https://hdl.handle.net/21.15107/rcub_dais_15978
Jović B, Lačnjevac U, Jović V, Gajić Krstajić L, Kovač J, Poleti D, Krstajić N. Ni-(Ebonex-supported Ir) composite coatings as electrocatalysts for alkaline water electrolysis. Part II: Oxygen evolution. in International Journal of Hydrogen Energy. 2016;41(45):20502-20514.
doi:10.1016/j.ijhydene.2016.08.226
https://hdl.handle.net/21.15107/rcub_dais_15978 .
Jović, Borka, Lačnjevac, Uroš, Jović, Vladimir, Gajić Krstajić, Ljiljana, Kovač, Janez, Poleti, Dejan, Krstajić, Nedeljko, "Ni-(Ebonex-supported Ir) composite coatings as electrocatalysts for alkaline water electrolysis. Part II: Oxygen evolution" in International Journal of Hydrogen Energy, 41, no. 45 (2016):20502-20514,
https://doi.org/10.1016/j.ijhydene.2016.08.226 .,
https://hdl.handle.net/21.15107/rcub_dais_15978 .
18
22
22

Phase composition of Bi2O3 specimens doped with Ti, Zr and Hf

Poleti, Dejan; Karanović, Ljiljana; Zdujić, Miodrag; Jovalekić, Čedomir

(Belgrade : Serbian Chemical Society, 2012)

TY  - JOUR
AU  - Poleti, Dejan
AU  - Karanović, Ljiljana
AU  - Zdujić, Miodrag
AU  - Jovalekić, Čedomir
PY  - 2012
UR  - http://dais.sanu.ac.rs/123456789/270
AB  - Powder mixtures of α-Bi2O3 containing 2, 5 and 10 mole % of TiO2, ZrO2 or HfO2 were homogenized, heated at 820ºC for 24 h and quenched in air. X-ray powder diffraction technique was used to characterize the prepared samples. In all cases metastable Bi2O3 polymorphs, γ-Bi2O3 or β-Bi2O3, are found as single or major phases. Addition of Ti4+ ions stabilizes γ-Bi2O3 polymorph, while either Zr4+ or Hf4+ ions stabilize β-Bi2O3 polymorph. In the samples with 2 and 5 mole % of TiO2 the presence of even two γ-Bi2O3 phases (Bi12TiO20 compound and a very low Ti-doped γ-Bi2O3) was established. Similarly, in the sample with 2 mole % of HfO2 two β-Bi2O3 phases were found. Phase composition of prepared samples, values of unit cell parameters and the appearance of two polymorphs with identical crystal structure but different unit cell parameters are discussed and compared with known data.
PB  - Belgrade : Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Phase composition of Bi2O3 specimens doped with Ti, Zr and Hf
SP  - 1091
EP  - 1096
VL  - 77
IS  - 8
DO  - 10.2298/JSC110914215P
UR  - https://hdl.handle.net/21.15107/rcub_dais_270
ER  - 
@article{
author = "Poleti, Dejan and Karanović, Ljiljana and Zdujić, Miodrag and Jovalekić, Čedomir",
year = "2012",
abstract = "Powder mixtures of α-Bi2O3 containing 2, 5 and 10 mole % of TiO2, ZrO2 or HfO2 were homogenized, heated at 820ºC for 24 h and quenched in air. X-ray powder diffraction technique was used to characterize the prepared samples. In all cases metastable Bi2O3 polymorphs, γ-Bi2O3 or β-Bi2O3, are found as single or major phases. Addition of Ti4+ ions stabilizes γ-Bi2O3 polymorph, while either Zr4+ or Hf4+ ions stabilize β-Bi2O3 polymorph. In the samples with 2 and 5 mole % of TiO2 the presence of even two γ-Bi2O3 phases (Bi12TiO20 compound and a very low Ti-doped γ-Bi2O3) was established. Similarly, in the sample with 2 mole % of HfO2 two β-Bi2O3 phases were found. Phase composition of prepared samples, values of unit cell parameters and the appearance of two polymorphs with identical crystal structure but different unit cell parameters are discussed and compared with known data.",
publisher = "Belgrade : Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Phase composition of Bi2O3 specimens doped with Ti, Zr and Hf",
pages = "1091-1096",
volume = "77",
number = "8",
doi = "10.2298/JSC110914215P",
url = "https://hdl.handle.net/21.15107/rcub_dais_270"
}
Poleti, D., Karanović, L., Zdujić, M.,& Jovalekić, Č.. (2012). Phase composition of Bi2O3 specimens doped with Ti, Zr and Hf. in Journal of the Serbian Chemical Society
Belgrade : Serbian Chemical Society., 77(8), 1091-1096.
https://doi.org/10.2298/JSC110914215P
https://hdl.handle.net/21.15107/rcub_dais_270
Poleti D, Karanović L, Zdujić M, Jovalekić Č. Phase composition of Bi2O3 specimens doped with Ti, Zr and Hf. in Journal of the Serbian Chemical Society. 2012;77(8):1091-1096.
doi:10.2298/JSC110914215P
https://hdl.handle.net/21.15107/rcub_dais_270 .
Poleti, Dejan, Karanović, Ljiljana, Zdujić, Miodrag, Jovalekić, Čedomir, "Phase composition of Bi2O3 specimens doped with Ti, Zr and Hf" in Journal of the Serbian Chemical Society, 77, no. 8 (2012):1091-1096,
https://doi.org/10.2298/JSC110914215P .,
https://hdl.handle.net/21.15107/rcub_dais_270 .
7
7
7

Solid state synthesis of extra phase-pure Li4Ti5O12 spinel

Veljković, Ivana; Poleti, Dejan; Karanović, Ljiljana; Zdujić, Miodrag; Branković, Goran

(Belgrade : International Institute for the Science of Sintering, 2011)

TY  - JOUR
AU  - Veljković, Ivana
AU  - Poleti, Dejan
AU  - Karanović, Ljiljana
AU  - Zdujić, Miodrag
AU  - Branković, Goran
PY  - 2011
UR  - http://dais.sanu.ac.rs/123456789/199
AB  - Extra phase-pure Li4Ti5O12 spinel with particle sizes less than 500 nm was synthesized by solid state reaction of mechanochemicaly activated mixture of nano anatase and Li2CO3 for a very short annealing time, 4 h at 800°C. Structural and microstructural properties, the mechanism of solid state reaction between anatase and Li2CO3 as well as thermal stability of prepared spinel were investigated using XRPD, SEM and TG/DSC analysis. The mechanism of reaction implies decomposition of Li2CO3 below 250ºC, formation of monoclinic Li2TiO3 as intermediate product between 400 and 600°C and its transformation to Li4Ti5O12 between 600-800ºC. The spinel structure is stable up to 1000ºC when it is decomposed due to Li2O evaporation.
PB  - Belgrade : International Institute for the Science of Sintering
T2  - Science of Sintering
T1  - Solid state synthesis of extra phase-pure Li4Ti5O12 spinel
SP  - 343
EP  - 351
VL  - 43
IS  - 3
DO  - 10.2298/SOS1103343V
UR  - https://hdl.handle.net/21.15107/rcub_dais_199
ER  - 
@article{
author = "Veljković, Ivana and Poleti, Dejan and Karanović, Ljiljana and Zdujić, Miodrag and Branković, Goran",
year = "2011",
abstract = "Extra phase-pure Li4Ti5O12 spinel with particle sizes less than 500 nm was synthesized by solid state reaction of mechanochemicaly activated mixture of nano anatase and Li2CO3 for a very short annealing time, 4 h at 800°C. Structural and microstructural properties, the mechanism of solid state reaction between anatase and Li2CO3 as well as thermal stability of prepared spinel were investigated using XRPD, SEM and TG/DSC analysis. The mechanism of reaction implies decomposition of Li2CO3 below 250ºC, formation of monoclinic Li2TiO3 as intermediate product between 400 and 600°C and its transformation to Li4Ti5O12 between 600-800ºC. The spinel structure is stable up to 1000ºC when it is decomposed due to Li2O evaporation.",
publisher = "Belgrade : International Institute for the Science of Sintering",
journal = "Science of Sintering",
title = "Solid state synthesis of extra phase-pure Li4Ti5O12 spinel",
pages = "343-351",
volume = "43",
number = "3",
doi = "10.2298/SOS1103343V",
url = "https://hdl.handle.net/21.15107/rcub_dais_199"
}
Veljković, I., Poleti, D., Karanović, L., Zdujić, M.,& Branković, G.. (2011). Solid state synthesis of extra phase-pure Li4Ti5O12 spinel. in Science of Sintering
Belgrade : International Institute for the Science of Sintering., 43(3), 343-351.
https://doi.org/10.2298/SOS1103343V
https://hdl.handle.net/21.15107/rcub_dais_199
Veljković I, Poleti D, Karanović L, Zdujić M, Branković G. Solid state synthesis of extra phase-pure Li4Ti5O12 spinel. in Science of Sintering. 2011;43(3):343-351.
doi:10.2298/SOS1103343V
https://hdl.handle.net/21.15107/rcub_dais_199 .
Veljković, Ivana, Poleti, Dejan, Karanović, Ljiljana, Zdujić, Miodrag, Branković, Goran, "Solid state synthesis of extra phase-pure Li4Ti5O12 spinel" in Science of Sintering, 43, no. 3 (2011):343-351,
https://doi.org/10.2298/SOS1103343V .,
https://hdl.handle.net/21.15107/rcub_dais_199 .
6
23
23
24

Mechanochemistry of titanium oxides

Veljković, Ivana; Poleti, Dejan; Zdujić, Miodrag; Karanović, Ljiljana

(Belgrade : Association of the Chemical Engineers of Serbia, 2009)

TY  - JOUR
AU  - Veljković, Ivana
AU  - Poleti, Dejan
AU  - Zdujić, Miodrag
AU  - Karanović, Ljiljana
PY  - 2009
UR  - http://dais.sanu.ac.rs/123456789/3458
AB  - Mechanochemistry represents an alternative route in synthesis of nanomaterials. Mechanochemical routes are attractive because of their simplicity, flexibility, and ability to prepare materials by solid state reactions at room temperature. The aim of this work is the mechanochemical synthesis of nanostructured titanium oxides of different composition starting from mixtures of Ti and TiO2, TiO and TiO2 or Ti 2O3 and TiO2. Emphasis is on the Magneli phases Ti4O7 and Ti5O9 because their mixture is commercially known as EBONEX material. The materials prepared were characterized by XRPD, TG/DTA analysis, SEM and optical microscopy. Titanium monoxide and several Magneli oxides, Ti4O7, Ti 5O9 and Ti6O11, are successsfully prepared. The results are very interesting because the EBONEX materials were prepared at lower than usual temperature, which would decrease the effective cost of production.
PB  - Belgrade : Association of the Chemical Engineers of Serbia
T2  - Hemijska industrija
T1  - Mechanochemistry of titanium oxides
SP  - 247
EP  - 251
VL  - 63
IS  - 3
DO  - 10.2298/HEMIND0903247V
UR  - https://hdl.handle.net/21.15107/rcub_dais_3458
ER  - 
@article{
author = "Veljković, Ivana and Poleti, Dejan and Zdujić, Miodrag and Karanović, Ljiljana",
year = "2009",
abstract = "Mechanochemistry represents an alternative route in synthesis of nanomaterials. Mechanochemical routes are attractive because of their simplicity, flexibility, and ability to prepare materials by solid state reactions at room temperature. The aim of this work is the mechanochemical synthesis of nanostructured titanium oxides of different composition starting from mixtures of Ti and TiO2, TiO and TiO2 or Ti 2O3 and TiO2. Emphasis is on the Magneli phases Ti4O7 and Ti5O9 because their mixture is commercially known as EBONEX material. The materials prepared were characterized by XRPD, TG/DTA analysis, SEM and optical microscopy. Titanium monoxide and several Magneli oxides, Ti4O7, Ti 5O9 and Ti6O11, are successsfully prepared. The results are very interesting because the EBONEX materials were prepared at lower than usual temperature, which would decrease the effective cost of production.",
publisher = "Belgrade : Association of the Chemical Engineers of Serbia",
journal = "Hemijska industrija",
title = "Mechanochemistry of titanium oxides",
pages = "247-251",
volume = "63",
number = "3",
doi = "10.2298/HEMIND0903247V",
url = "https://hdl.handle.net/21.15107/rcub_dais_3458"
}
Veljković, I., Poleti, D., Zdujić, M.,& Karanović, L.. (2009). Mechanochemistry of titanium oxides. in Hemijska industrija
Belgrade : Association of the Chemical Engineers of Serbia., 63(3), 247-251.
https://doi.org/10.2298/HEMIND0903247V
https://hdl.handle.net/21.15107/rcub_dais_3458
Veljković I, Poleti D, Zdujić M, Karanović L. Mechanochemistry of titanium oxides. in Hemijska industrija. 2009;63(3):247-251.
doi:10.2298/HEMIND0903247V
https://hdl.handle.net/21.15107/rcub_dais_3458 .
Veljković, Ivana, Poleti, Dejan, Zdujić, Miodrag, Karanović, Ljiljana, "Mechanochemistry of titanium oxides" in Hemijska industrija, 63, no. 3 (2009):247-251,
https://doi.org/10.2298/HEMIND0903247V .,
https://hdl.handle.net/21.15107/rcub_dais_3458 .
1
1
1

Mechanochemically induced amorphous/crystalline phase transition in the Bi4Ti3O12 compound

Zdujić, Miodrag; Jovalekić, Čedomir; Poleti, Dejan; Veljković, Ivana; Karanović, Ljiljana

(Elsevier, 2009)

TY  - JOUR
AU  - Zdujić, Miodrag
AU  - Jovalekić, Čedomir
AU  - Poleti, Dejan
AU  - Veljković, Ivana
AU  - Karanović, Ljiljana
PY  - 2009
UR  - http://dais.sanu.ac.rs/123456789/3454
AB  - Concurrent milling of Bi4Ti3O12 was carried out in a planetary ball mill with hardened-steel 13 or 6 mm diameter balls with a goal to investigate how the system responds to the constrains imposed by milling. Milling intensity for various milling parameters was derived from the electrical power measurement. The reverse amorphous ↔ crystalline phase transition induced by milling is governed by impact energy and frequency. Below a certain threshold value of impact energy crystallization does not occur, whereas a higher impact frequency accelerates amorphization. Mechanochemical reactions are predominantly discrete processes, which occur at the moment of impact. © 2009 Elsevier B.V. All rights reserved.
PB  - Elsevier
T2  - Materials Letters
T1  - Mechanochemically induced amorphous/crystalline phase transition in the Bi4Ti3O12 compound
SP  - 2542
EP  - 2544
VL  - 63
IS  - 29
DO  - 10.1016/j.matlet.2009.08.055
UR  - https://hdl.handle.net/21.15107/rcub_dais_3454
ER  - 
@article{
author = "Zdujić, Miodrag and Jovalekić, Čedomir and Poleti, Dejan and Veljković, Ivana and Karanović, Ljiljana",
year = "2009",
abstract = "Concurrent milling of Bi4Ti3O12 was carried out in a planetary ball mill with hardened-steel 13 or 6 mm diameter balls with a goal to investigate how the system responds to the constrains imposed by milling. Milling intensity for various milling parameters was derived from the electrical power measurement. The reverse amorphous ↔ crystalline phase transition induced by milling is governed by impact energy and frequency. Below a certain threshold value of impact energy crystallization does not occur, whereas a higher impact frequency accelerates amorphization. Mechanochemical reactions are predominantly discrete processes, which occur at the moment of impact. © 2009 Elsevier B.V. All rights reserved.",
publisher = "Elsevier",
journal = "Materials Letters",
title = "Mechanochemically induced amorphous/crystalline phase transition in the Bi4Ti3O12 compound",
pages = "2542-2544",
volume = "63",
number = "29",
doi = "10.1016/j.matlet.2009.08.055",
url = "https://hdl.handle.net/21.15107/rcub_dais_3454"
}
Zdujić, M., Jovalekić, Č., Poleti, D., Veljković, I.,& Karanović, L.. (2009). Mechanochemically induced amorphous/crystalline phase transition in the Bi4Ti3O12 compound. in Materials Letters
Elsevier., 63(29), 2542-2544.
https://doi.org/10.1016/j.matlet.2009.08.055
https://hdl.handle.net/21.15107/rcub_dais_3454
Zdujić M, Jovalekić Č, Poleti D, Veljković I, Karanović L. Mechanochemically induced amorphous/crystalline phase transition in the Bi4Ti3O12 compound. in Materials Letters. 2009;63(29):2542-2544.
doi:10.1016/j.matlet.2009.08.055
https://hdl.handle.net/21.15107/rcub_dais_3454 .
Zdujić, Miodrag, Jovalekić, Čedomir, Poleti, Dejan, Veljković, Ivana, Karanović, Ljiljana, "Mechanochemically induced amorphous/crystalline phase transition in the Bi4Ti3O12 compound" in Materials Letters, 63, no. 29 (2009):2542-2544,
https://doi.org/10.1016/j.matlet.2009.08.055 .,
https://hdl.handle.net/21.15107/rcub_dais_3454 .
3
2
3

Mechanochemical synthesis and electrical conductivity of nanocrystalline δ-Bi2O3 stabilized by HfO2 and ZrO2

Zdujić, Miodrag; Poleti, Dejan; Jovalekić, Čedomir; Karanović, Ljiljana

(Belgrade : Serbian Chemical Society, 2009)

TY  - JOUR
AU  - Zdujić, Miodrag
AU  - Poleti, Dejan
AU  - Jovalekić, Čedomir
AU  - Karanović, Ljiljana
PY  - 2009
UR  - http://dais.sanu.ac.rs/123456789/174
AB  - A powder mixture of α-Bi2O3 and HfO2, in the molar ratio 2:3, was mechanochemically treated in a planetary ball mill under air, using zirconium oxide vials and balls as the milling medium. After 50 h of milling, the mechanochemical reaction led to the formation of a nanocrystalline δ-Bi2O3 phase (fluorite-type solid solution Bi0.78Hf0.59Zr0.63O3.61), with a crystallite size of 20 nm. The mechanochemical reaction started at a very beginning of milling accompanied by an accumulation of ZrO2 arising from the milling tools. The samples prepared after various milling times were characterized by X-ray powder diffraction and DSC analysis. The electrical properties of the as-milled and pressed Bi0.78Hf0.59Zr0.63O3.61 powder were studied using impedance spectroscopy in the temperature range from 100 to 700°C under air. The electrical conductivity was determined to be 9.43×10-6 and 0.080 S cm-1 for the temperatures of 300 and 700°C, respectively.
AB  - Smeša prahova α-Bi2O3 i HfO2 u molarnom odnosu 2:3 mehanohemijski je tretirana u planetarnom mlinu u atmosferi vazduha, koristeći cirkonijumske posude i kuglice kao medijum za mlevenje. Posle 50 h mlevenja, mehanohemijska reakcija dovodi do stvaranja nanokristalne δ-Bi2O3 faze (čvrsti rastvor fluoritske strukture Bi0,78Hf0,59Zr0,63O3,61), veličine kristalita 20 nm. Mehanohemijska reakcija otpočinje u samom početku mlevenja i praćena je akumulacijum ZrO2 koji potiče od medijuma za mlevenje. Uzorci dobijeni posle različitih vremena mlevenja karakterisani su rendgenskom strukturnom i termijskom analizom. Električna svojstva mlevenih i presovanih Bi0,78Hf0,59Zr0,63O3,61 prahova ispitivana su impedansnom spektroskopijom u temperaturnom opsegu od 100 do 700°C. Dobijena električna provodnost je 9,43·10-6 i 0,080 S cm-1 za temperaturu 300 i 700°C, redom.
PB  - Belgrade : Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Mechanochemical synthesis and electrical conductivity of nanocrystalline δ-Bi2O3 stabilized by HfO2 and ZrO2
SP  - 1401
EP  - 1411
VL  - 74
IS  - 12
DO  - 10.2298/JSC0912401Z
UR  - https://hdl.handle.net/21.15107/rcub_dais_174
ER  - 
@article{
author = "Zdujić, Miodrag and Poleti, Dejan and Jovalekić, Čedomir and Karanović, Ljiljana",
year = "2009",
abstract = "A powder mixture of α-Bi2O3 and HfO2, in the molar ratio 2:3, was mechanochemically treated in a planetary ball mill under air, using zirconium oxide vials and balls as the milling medium. After 50 h of milling, the mechanochemical reaction led to the formation of a nanocrystalline δ-Bi2O3 phase (fluorite-type solid solution Bi0.78Hf0.59Zr0.63O3.61), with a crystallite size of 20 nm. The mechanochemical reaction started at a very beginning of milling accompanied by an accumulation of ZrO2 arising from the milling tools. The samples prepared after various milling times were characterized by X-ray powder diffraction and DSC analysis. The electrical properties of the as-milled and pressed Bi0.78Hf0.59Zr0.63O3.61 powder were studied using impedance spectroscopy in the temperature range from 100 to 700°C under air. The electrical conductivity was determined to be 9.43×10-6 and 0.080 S cm-1 for the temperatures of 300 and 700°C, respectively., Smeša prahova α-Bi2O3 i HfO2 u molarnom odnosu 2:3 mehanohemijski je tretirana u planetarnom mlinu u atmosferi vazduha, koristeći cirkonijumske posude i kuglice kao medijum za mlevenje. Posle 50 h mlevenja, mehanohemijska reakcija dovodi do stvaranja nanokristalne δ-Bi2O3 faze (čvrsti rastvor fluoritske strukture Bi0,78Hf0,59Zr0,63O3,61), veličine kristalita 20 nm. Mehanohemijska reakcija otpočinje u samom početku mlevenja i praćena je akumulacijum ZrO2 koji potiče od medijuma za mlevenje. Uzorci dobijeni posle različitih vremena mlevenja karakterisani su rendgenskom strukturnom i termijskom analizom. Električna svojstva mlevenih i presovanih Bi0,78Hf0,59Zr0,63O3,61 prahova ispitivana su impedansnom spektroskopijom u temperaturnom opsegu od 100 do 700°C. Dobijena električna provodnost je 9,43·10-6 i 0,080 S cm-1 za temperaturu 300 i 700°C, redom.",
publisher = "Belgrade : Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Mechanochemical synthesis and electrical conductivity of nanocrystalline δ-Bi2O3 stabilized by HfO2 and ZrO2",
pages = "1401-1411",
volume = "74",
number = "12",
doi = "10.2298/JSC0912401Z",
url = "https://hdl.handle.net/21.15107/rcub_dais_174"
}
Zdujić, M., Poleti, D., Jovalekić, Č.,& Karanović, L.. (2009). Mechanochemical synthesis and electrical conductivity of nanocrystalline δ-Bi2O3 stabilized by HfO2 and ZrO2. in Journal of the Serbian Chemical Society
Belgrade : Serbian Chemical Society., 74(12), 1401-1411.
https://doi.org/10.2298/JSC0912401Z
https://hdl.handle.net/21.15107/rcub_dais_174
Zdujić M, Poleti D, Jovalekić Č, Karanović L. Mechanochemical synthesis and electrical conductivity of nanocrystalline δ-Bi2O3 stabilized by HfO2 and ZrO2. in Journal of the Serbian Chemical Society. 2009;74(12):1401-1411.
doi:10.2298/JSC0912401Z
https://hdl.handle.net/21.15107/rcub_dais_174 .
Zdujić, Miodrag, Poleti, Dejan, Jovalekić, Čedomir, Karanović, Ljiljana, "Mechanochemical synthesis and electrical conductivity of nanocrystalline δ-Bi2O3 stabilized by HfO2 and ZrO2" in Journal of the Serbian Chemical Society, 74, no. 12 (2009):1401-1411,
https://doi.org/10.2298/JSC0912401Z .,
https://hdl.handle.net/21.15107/rcub_dais_174 .
8
10
10

Structural and electrical properties of the 2Bi2O3·3ZrO2 system

Jovalekić, Čedomir; Zdujić, Miodrag; Poleti, Dejan; Karanović, Ljiljana; Mitrić, Miodrag

(2008)

TY  - JOUR
AU  - Jovalekić, Čedomir
AU  - Zdujić, Miodrag
AU  - Poleti, Dejan
AU  - Karanović, Ljiljana
AU  - Mitrić, Miodrag
PY  - 2008
UR  - http://dais.sanu.ac.rs/123456789/3582
AB  - Powder mixtures of α-Bi2O3 (bismite) and monoclinic m-ZrO2 (baddeleyite) in the molar ratio 2:3 were mechanochemically and thermally treated with the goal to examine the phases, which may appear during such procedures. The prepared samples were characterized by X-ray powder diffraction, differential scanning calorimetry (DSC), electrical measurements, as well as scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The mechanochemical reaction leads to the gradual formation of a nanocrystalline phase, which resembles δ-Bi2O3, a high-temperature Bi2O3 polymorph. Isothermal sintering in air at a temperature of 820 °C for 24 h followed by quenching to room temperature yielded a mixture of ZrO2-stabilized β-Bi2O3 and m-ZrO2 phases, whereas in slowly cooled products, the complete separation of the initial α-Bi2O3 and m-ZrO2 constituents was observed. The dielectric permittivity of the sintered samples significantly depended on the temperature. The sintered and quenched samples exhibited a hysteresis dependence of the dielectric shift, showing that the ZrO2-doped β-Bi2O3 phase possess ferroelectric properties, which were detected for the first time. This fact, together with Rietveld refinement of the β-Bi2O3/m-ZrO2 mixture based on neutron powder diffraction data showed that ZrO2-doped β-Bi2O3 has a non-centrosymmetric structure with P over(4, -) 21 c as the true space group. The ZrO2 content in the doped β-Bi2O3 and the crystal chemical reasons for the stabilization of the β-Bi2O3 phase by the addition of m-ZrO2 are discussed. © 2008 Elsevier Inc. All rights reserved.
T2  - Journal of Solid State Chemistry
T1  - Structural and electrical properties of the 2Bi2O3·3ZrO2 system
SP  - 1321
EP  - 1329
VL  - 181
IS  - 6
DO  - 10.1016/j.jssc.2008.02.038
UR  - https://hdl.handle.net/21.15107/rcub_dais_3582
ER  - 
@article{
author = "Jovalekić, Čedomir and Zdujić, Miodrag and Poleti, Dejan and Karanović, Ljiljana and Mitrić, Miodrag",
year = "2008",
abstract = "Powder mixtures of α-Bi2O3 (bismite) and monoclinic m-ZrO2 (baddeleyite) in the molar ratio 2:3 were mechanochemically and thermally treated with the goal to examine the phases, which may appear during such procedures. The prepared samples were characterized by X-ray powder diffraction, differential scanning calorimetry (DSC), electrical measurements, as well as scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The mechanochemical reaction leads to the gradual formation of a nanocrystalline phase, which resembles δ-Bi2O3, a high-temperature Bi2O3 polymorph. Isothermal sintering in air at a temperature of 820 °C for 24 h followed by quenching to room temperature yielded a mixture of ZrO2-stabilized β-Bi2O3 and m-ZrO2 phases, whereas in slowly cooled products, the complete separation of the initial α-Bi2O3 and m-ZrO2 constituents was observed. The dielectric permittivity of the sintered samples significantly depended on the temperature. The sintered and quenched samples exhibited a hysteresis dependence of the dielectric shift, showing that the ZrO2-doped β-Bi2O3 phase possess ferroelectric properties, which were detected for the first time. This fact, together with Rietveld refinement of the β-Bi2O3/m-ZrO2 mixture based on neutron powder diffraction data showed that ZrO2-doped β-Bi2O3 has a non-centrosymmetric structure with P over(4, -) 21 c as the true space group. The ZrO2 content in the doped β-Bi2O3 and the crystal chemical reasons for the stabilization of the β-Bi2O3 phase by the addition of m-ZrO2 are discussed. © 2008 Elsevier Inc. All rights reserved.",
journal = "Journal of Solid State Chemistry",
title = "Structural and electrical properties of the 2Bi2O3·3ZrO2 system",
pages = "1321-1329",
volume = "181",
number = "6",
doi = "10.1016/j.jssc.2008.02.038",
url = "https://hdl.handle.net/21.15107/rcub_dais_3582"
}
Jovalekić, Č., Zdujić, M., Poleti, D., Karanović, L.,& Mitrić, M.. (2008). Structural and electrical properties of the 2Bi2O3·3ZrO2 system. in Journal of Solid State Chemistry, 181(6), 1321-1329.
https://doi.org/10.1016/j.jssc.2008.02.038
https://hdl.handle.net/21.15107/rcub_dais_3582
Jovalekić Č, Zdujić M, Poleti D, Karanović L, Mitrić M. Structural and electrical properties of the 2Bi2O3·3ZrO2 system. in Journal of Solid State Chemistry. 2008;181(6):1321-1329.
doi:10.1016/j.jssc.2008.02.038
https://hdl.handle.net/21.15107/rcub_dais_3582 .
Jovalekić, Čedomir, Zdujić, Miodrag, Poleti, Dejan, Karanović, Ljiljana, Mitrić, Miodrag, "Structural and electrical properties of the 2Bi2O3·3ZrO2 system" in Journal of Solid State Chemistry, 181, no. 6 (2008):1321-1329,
https://doi.org/10.1016/j.jssc.2008.02.038 .,
https://hdl.handle.net/21.15107/rcub_dais_3582 .
21
20
24

Mechanochemical synthesis of nanocrystalline titanium monoxide

Veljković, Ivana; Poleti, Dejan; Zdujić, Miodrag; Karanović, Ljiljana; Jovalekić, Čedomir

(Elsevier, 2008)

TY  - JOUR
AU  - Veljković, Ivana
AU  - Poleti, Dejan
AU  - Zdujić, Miodrag
AU  - Karanović, Ljiljana
AU  - Jovalekić, Čedomir
PY  - 2008
UR  - http://dais.sanu.ac.rs/123456789/3580
AB  - Nanocrystalline cubic titanium monoxide, TiOx (0.92 < x < 1.19), with mean crystallite size of ≈ 6 nm, was synthesized by mechanochemical treatment of Ti and TiO2 (rutile) powder mixtures with molar ratios of 1:1, 1.10:1 and 1.25:1. The mechanochemical solid state reaction in a high-energy planetary ball mill was completed for 2 h in either air or argon atmosphere. During heating in vacuum at 900 and 1000 °C for 24 h, nanocrystalline TiOx transforms to a well-crystallized, cubic or monoclinic TiOx. The materials prepared were characterized by XRPD, TGA/DSC and SEM/EDS analysis. © 2008 Elsevier B.V. All rights reserved.
PB  - Elsevier
T2  - Materials Letters
T1  - Mechanochemical synthesis of nanocrystalline titanium monoxide
SP  - 2769
EP  - 2771
VL  - 62
IS  - 17-18
DO  - 10.1016/j.matlet.2008.01.039
UR  - https://hdl.handle.net/21.15107/rcub_dais_3580
ER  - 
@article{
author = "Veljković, Ivana and Poleti, Dejan and Zdujić, Miodrag and Karanović, Ljiljana and Jovalekić, Čedomir",
year = "2008",
abstract = "Nanocrystalline cubic titanium monoxide, TiOx (0.92 < x < 1.19), with mean crystallite size of ≈ 6 nm, was synthesized by mechanochemical treatment of Ti and TiO2 (rutile) powder mixtures with molar ratios of 1:1, 1.10:1 and 1.25:1. The mechanochemical solid state reaction in a high-energy planetary ball mill was completed for 2 h in either air or argon atmosphere. During heating in vacuum at 900 and 1000 °C for 24 h, nanocrystalline TiOx transforms to a well-crystallized, cubic or monoclinic TiOx. The materials prepared were characterized by XRPD, TGA/DSC and SEM/EDS analysis. © 2008 Elsevier B.V. All rights reserved.",
publisher = "Elsevier",
journal = "Materials Letters",
title = "Mechanochemical synthesis of nanocrystalline titanium monoxide",
pages = "2769-2771",
volume = "62",
number = "17-18",
doi = "10.1016/j.matlet.2008.01.039",
url = "https://hdl.handle.net/21.15107/rcub_dais_3580"
}
Veljković, I., Poleti, D., Zdujić, M., Karanović, L.,& Jovalekić, Č.. (2008). Mechanochemical synthesis of nanocrystalline titanium monoxide. in Materials Letters
Elsevier., 62(17-18), 2769-2771.
https://doi.org/10.1016/j.matlet.2008.01.039
https://hdl.handle.net/21.15107/rcub_dais_3580
Veljković I, Poleti D, Zdujić M, Karanović L, Jovalekić Č. Mechanochemical synthesis of nanocrystalline titanium monoxide. in Materials Letters. 2008;62(17-18):2769-2771.
doi:10.1016/j.matlet.2008.01.039
https://hdl.handle.net/21.15107/rcub_dais_3580 .
Veljković, Ivana, Poleti, Dejan, Zdujić, Miodrag, Karanović, Ljiljana, Jovalekić, Čedomir, "Mechanochemical synthesis of nanocrystalline titanium monoxide" in Materials Letters, 62, no. 17-18 (2008):2769-2771,
https://doi.org/10.1016/j.matlet.2008.01.039 .,
https://hdl.handle.net/21.15107/rcub_dais_3580 .
20
21
22

Uticaj parametara mlevenja na odnos amorfne i kristalne faze u jedinjenju Bi4Ti3O12

Zdujić, Miodrag; Jovalekić, Čedomir; Veljković, Ivana; Poleti, Dejan; Karanović, Ljiljana

(2008)

TY  - CONF
AU  - Zdujić, Miodrag
AU  - Jovalekić, Čedomir
AU  - Veljković, Ivana
AU  - Poleti, Dejan
AU  - Karanović, Ljiljana
PY  - 2008
UR  - http://dais.sanu.ac.rs/123456789/302
AB  - Poster presented at the XLVI Savetovanje srpskog hemijskog društva, Beograd, 29. mart (21. februar) 2008
T1  - Uticaj parametara mlevenja na odnos amorfne i kristalne faze u jedinjenju Bi4Ti3O12
UR  - https://hdl.handle.net/21.15107/rcub_dais_302
ER  - 
@conference{
author = "Zdujić, Miodrag and Jovalekić, Čedomir and Veljković, Ivana and Poleti, Dejan and Karanović, Ljiljana",
year = "2008",
abstract = "Poster presented at the XLVI Savetovanje srpskog hemijskog društva, Beograd, 29. mart (21. februar) 2008",
title = "Uticaj parametara mlevenja na odnos amorfne i kristalne faze u jedinjenju Bi4Ti3O12",
url = "https://hdl.handle.net/21.15107/rcub_dais_302"
}
Zdujić, M., Jovalekić, Č., Veljković, I., Poleti, D.,& Karanović, L.. (2008). Uticaj parametara mlevenja na odnos amorfne i kristalne faze u jedinjenju Bi4Ti3O12. .
https://hdl.handle.net/21.15107/rcub_dais_302
Zdujić M, Jovalekić Č, Veljković I, Poleti D, Karanović L. Uticaj parametara mlevenja na odnos amorfne i kristalne faze u jedinjenju Bi4Ti3O12. 2008;.
https://hdl.handle.net/21.15107/rcub_dais_302 .
Zdujić, Miodrag, Jovalekić, Čedomir, Veljković, Ivana, Poleti, Dejan, Karanović, Ljiljana, "Uticaj parametara mlevenja na odnos amorfne i kristalne faze u jedinjenju Bi4Ti3O12" (2008),
https://hdl.handle.net/21.15107/rcub_dais_302 .

ZnO varistors prepared by direct mixing of constituent phases

Branković, Zorica; Milošević, Olivera; Poleti, Dejan; Karanović, Ljiljana; Uskoković, Dragan

(Sendai : Japan Institute of Metals, 2000)

TY  - JOUR
AU  - Branković, Zorica
AU  - Milošević, Olivera
AU  - Poleti, Dejan
AU  - Karanović, Ljiljana
AU  - Uskoković, Dragan
PY  - 2000
UR  - http://dais.sanu.ac.rs/123456789/3865
AB  - ZnO varistors with non-linearity coefficients reaching 50 and low values of the leakage current (approximately 0.01 A/m2), were obtained by a method referred to as `direct mixing of constituent phases'. The method is based on sintering of a mixture of the constituent phases with the following compositions: ZnO phase uniformly doped with Co2+ and Mn2+; intergranular phase: γ-Bi2O3 stabilized with Mn2+ or Zn2+; spinel phase: Zn1.971Ni0.090Co0.030Cr0.247Mn0.090Sb0.545O4. As proved, the obtained varistors are composed of the same phases as those introduced into the system. The influence of composition as well as milling and sintering parameters on the varistor characteristics were investigated. Some varistor powder mixtures were intensively milled before sintering. As a result, high density ceramics with highly homogeneous microstructure were obtained after sintering.
PB  - Sendai : Japan Institute of Metals
T2  - Materials Transactions, JIM
T1  - ZnO varistors prepared by direct mixing of constituent phases
SP  - 1226
EP  - 1231
VL  - 41
IS  - 9
DO  - 10.2320/matertrans1989.41.1226
UR  - https://hdl.handle.net/21.15107/rcub_dais_3865
ER  - 
@article{
author = "Branković, Zorica and Milošević, Olivera and Poleti, Dejan and Karanović, Ljiljana and Uskoković, Dragan",
year = "2000",
abstract = "ZnO varistors with non-linearity coefficients reaching 50 and low values of the leakage current (approximately 0.01 A/m2), were obtained by a method referred to as `direct mixing of constituent phases'. The method is based on sintering of a mixture of the constituent phases with the following compositions: ZnO phase uniformly doped with Co2+ and Mn2+; intergranular phase: γ-Bi2O3 stabilized with Mn2+ or Zn2+; spinel phase: Zn1.971Ni0.090Co0.030Cr0.247Mn0.090Sb0.545O4. As proved, the obtained varistors are composed of the same phases as those introduced into the system. The influence of composition as well as milling and sintering parameters on the varistor characteristics were investigated. Some varistor powder mixtures were intensively milled before sintering. As a result, high density ceramics with highly homogeneous microstructure were obtained after sintering.",
publisher = "Sendai : Japan Institute of Metals",
journal = "Materials Transactions, JIM",
title = "ZnO varistors prepared by direct mixing of constituent phases",
pages = "1226-1231",
volume = "41",
number = "9",
doi = "10.2320/matertrans1989.41.1226",
url = "https://hdl.handle.net/21.15107/rcub_dais_3865"
}
Branković, Z., Milošević, O., Poleti, D., Karanović, L.,& Uskoković, D.. (2000). ZnO varistors prepared by direct mixing of constituent phases. in Materials Transactions, JIM
Sendai : Japan Institute of Metals., 41(9), 1226-1231.
https://doi.org/10.2320/matertrans1989.41.1226
https://hdl.handle.net/21.15107/rcub_dais_3865
Branković Z, Milošević O, Poleti D, Karanović L, Uskoković D. ZnO varistors prepared by direct mixing of constituent phases. in Materials Transactions, JIM. 2000;41(9):1226-1231.
doi:10.2320/matertrans1989.41.1226
https://hdl.handle.net/21.15107/rcub_dais_3865 .
Branković, Zorica, Milošević, Olivera, Poleti, Dejan, Karanović, Ljiljana, Uskoković, Dragan, "ZnO varistors prepared by direct mixing of constituent phases" in Materials Transactions, JIM, 41, no. 9 (2000):1226-1231,
https://doi.org/10.2320/matertrans1989.41.1226 .,
https://hdl.handle.net/21.15107/rcub_dais_3865 .
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