Djosic, M. S.

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  • Djosic, M. S. (4)
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Author's Bibliography

The effect of applied current density on the surface morphology of deposited calcium phosphate coatings on titanium

Djosic, M. S.; Panić, Vladimir; Stojanovic, J.; Mitrić, Miodrag; Mišković-Stanković, Vesna B.

(2012)

TY  - JOUR
AU  - Djosic, M. S.
AU  - Panić, Vladimir
AU  - Stojanovic, J.
AU  - Mitrić, Miodrag
AU  - Mišković-Stanković, Vesna B.
PY  - 2012
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/4840
AB  - Electrochemical deposition of calcium phosphate coatings on titanium was performed galvanostatically from the aqueous solution of Ca(NO3)(2) and NH4H2PO4 with the current densities between 5.0 and 10 mA cm(-2), for different deposition times, at room temperature. The coatings were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The XRD results showed that dicalcium phosphate dihydrate (DCPD), brushite (CaHPO4 center dot 2H(2)O) coatings were deposited. The influence of applied current density and the deposition time on the phase composition, crystallite domain size and the morphology of brushite coatings were investigated. It was shown that brushite coating of the greatest mass was obtained for the longest deposition time, while the increase in current density over 7 mA cm(-2) does not affect significantly the mass of brushite coatings. The finest crystallites, with the smallest crystallite domain size of 15.6nm, were deposited at the current density of 9.0 mA cm(-2). Brushite coatings were fully converted to hydroxyapatite in simulated body fluid (SBF) which was confirmed by XRD and SEM. The crystallite domain size of HA coatings is controlled by applied current density for brushite coatings deposition: crystallization of HA at more porous brushite coatings, deposited at higher current density, caused the formation of smaller crystallites of hydroxyapatite. (C) 2012 Elsevier B.V. All rights reserved.
T2  - Colloids and Surfaces. A: Physicochemical and Engineering Aspects
T1  - The effect of applied current density on the surface morphology of deposited calcium phosphate coatings on titanium
VL  - 400
SP  - 36
EP  - 43
DO  - 10.1016/j.colsurfa.2012.02.040
ER  - 
@article{
author = "Djosic, M. S. and Panić, Vladimir and Stojanovic, J. and Mitrić, Miodrag and Mišković-Stanković, Vesna B.",
year = "2012",
abstract = "Electrochemical deposition of calcium phosphate coatings on titanium was performed galvanostatically from the aqueous solution of Ca(NO3)(2) and NH4H2PO4 with the current densities between 5.0 and 10 mA cm(-2), for different deposition times, at room temperature. The coatings were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The XRD results showed that dicalcium phosphate dihydrate (DCPD), brushite (CaHPO4 center dot 2H(2)O) coatings were deposited. The influence of applied current density and the deposition time on the phase composition, crystallite domain size and the morphology of brushite coatings were investigated. It was shown that brushite coating of the greatest mass was obtained for the longest deposition time, while the increase in current density over 7 mA cm(-2) does not affect significantly the mass of brushite coatings. The finest crystallites, with the smallest crystallite domain size of 15.6nm, were deposited at the current density of 9.0 mA cm(-2). Brushite coatings were fully converted to hydroxyapatite in simulated body fluid (SBF) which was confirmed by XRD and SEM. The crystallite domain size of HA coatings is controlled by applied current density for brushite coatings deposition: crystallization of HA at more porous brushite coatings, deposited at higher current density, caused the formation of smaller crystallites of hydroxyapatite. (C) 2012 Elsevier B.V. All rights reserved.",
journal = "Colloids and Surfaces. A: Physicochemical and Engineering Aspects",
title = "The effect of applied current density on the surface morphology of deposited calcium phosphate coatings on titanium",
volume = "400",
pages = "36-43",
doi = "10.1016/j.colsurfa.2012.02.040"
}
Djosic, M. S., Panić, V., Stojanovic, J., Mitrić, M.,& Mišković-Stanković, V. B.. (2012). The effect of applied current density on the surface morphology of deposited calcium phosphate coatings on titanium. in Colloids and Surfaces. A: Physicochemical and Engineering Aspects, 400, 36-43.
https://doi.org/10.1016/j.colsurfa.2012.02.040
Djosic MS, Panić V, Stojanovic J, Mitrić M, Mišković-Stanković VB. The effect of applied current density on the surface morphology of deposited calcium phosphate coatings on titanium. in Colloids and Surfaces. A: Physicochemical and Engineering Aspects. 2012;400:36-43.
doi:10.1016/j.colsurfa.2012.02.040 .
Djosic, M. S., Panić, Vladimir, Stojanovic, J., Mitrić, Miodrag, Mišković-Stanković, Vesna B., "The effect of applied current density on the surface morphology of deposited calcium phosphate coatings on titanium" in Colloids and Surfaces. A: Physicochemical and Engineering Aspects, 400 (2012):36-43,
https://doi.org/10.1016/j.colsurfa.2012.02.040 . .
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Electrodeposited hydroxyapatite thin films modified by ion beam irradiation

Djosic, M. S.; Bibić, Nataša M.; Mitrić, Miodrag; Šiljegović, Milorad; Stojanovic, J. N.; Jokić, Bojan M.; Janaćković, Đorđe T.; Mišković-Stanković, Vesna B.

(2009)

TY  - JOUR
AU  - Djosic, M. S.
AU  - Bibić, Nataša M.
AU  - Mitrić, Miodrag
AU  - Šiljegović, Milorad
AU  - Stojanovic, J. N.
AU  - Jokić, Bojan M.
AU  - Janaćković, Đorđe T.
AU  - Mišković-Stanković, Vesna B.
PY  - 2009
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/3872
AB  - Surface modification of hydroxyapatite (HA) thin films electrodeposited on titanium was conducted by ion implantation, using nitrogen and argon ions at different constant fluences of 1x10(15), 1x10(16) and 1x10(17) ions/cm(2). SEM and XRD analysis, as well as SRIM calculation, were used to monitor the changes induced by ion bombardment. In the case of HA film implanted with N(4+) ions, the unit cell parameters and unit cell volume increase with increasing nitrogen ion fluences. Similarly, the unit cell parameters and unit cell volume increase after Ar(6+) ions irradiation to a 1x10(15) ions/cm(2). At higher fluences, the unit cell parameters and unit cell volume decrease when argon ion fluences increase to 1x10(16) and 1x10(17) ions/cm(2). These structural changes are consequence of different mechanism of energy transfer of nitrogen and argon ions to HA film. For nitrogen ion irradiation electron energy loss is predominant, while for argon ion irradiation nuclear energy transfer to HA film prevails.
T2  - Journal of Optoelectronics and Advanced Materials
T1  - Electrodeposited hydroxyapatite thin films modified by ion beam irradiation
VL  - 11
IS  - 11
SP  - 1848
EP  - 1854
UR  - https://hdl.handle.net/21.15107/rcub_vinar_3872
ER  - 
@article{
author = "Djosic, M. S. and Bibić, Nataša M. and Mitrić, Miodrag and Šiljegović, Milorad and Stojanovic, J. N. and Jokić, Bojan M. and Janaćković, Đorđe T. and Mišković-Stanković, Vesna B.",
year = "2009",
abstract = "Surface modification of hydroxyapatite (HA) thin films electrodeposited on titanium was conducted by ion implantation, using nitrogen and argon ions at different constant fluences of 1x10(15), 1x10(16) and 1x10(17) ions/cm(2). SEM and XRD analysis, as well as SRIM calculation, were used to monitor the changes induced by ion bombardment. In the case of HA film implanted with N(4+) ions, the unit cell parameters and unit cell volume increase with increasing nitrogen ion fluences. Similarly, the unit cell parameters and unit cell volume increase after Ar(6+) ions irradiation to a 1x10(15) ions/cm(2). At higher fluences, the unit cell parameters and unit cell volume decrease when argon ion fluences increase to 1x10(16) and 1x10(17) ions/cm(2). These structural changes are consequence of different mechanism of energy transfer of nitrogen and argon ions to HA film. For nitrogen ion irradiation electron energy loss is predominant, while for argon ion irradiation nuclear energy transfer to HA film prevails.",
journal = "Journal of Optoelectronics and Advanced Materials",
title = "Electrodeposited hydroxyapatite thin films modified by ion beam irradiation",
volume = "11",
number = "11",
pages = "1848-1854",
url = "https://hdl.handle.net/21.15107/rcub_vinar_3872"
}
Djosic, M. S., Bibić, N. M., Mitrić, M., Šiljegović, M., Stojanovic, J. N., Jokić, B. M., Janaćković, Đ. T.,& Mišković-Stanković, V. B.. (2009). Electrodeposited hydroxyapatite thin films modified by ion beam irradiation. in Journal of Optoelectronics and Advanced Materials, 11(11), 1848-1854.
https://hdl.handle.net/21.15107/rcub_vinar_3872
Djosic MS, Bibić NM, Mitrić M, Šiljegović M, Stojanovic JN, Jokić BM, Janaćković ĐT, Mišković-Stanković VB. Electrodeposited hydroxyapatite thin films modified by ion beam irradiation. in Journal of Optoelectronics and Advanced Materials. 2009;11(11):1848-1854.
https://hdl.handle.net/21.15107/rcub_vinar_3872 .
Djosic, M. S., Bibić, Nataša M., Mitrić, Miodrag, Šiljegović, Milorad, Stojanovic, J. N., Jokić, Bojan M., Janaćković, Đorđe T., Mišković-Stanković, Vesna B., "Electrodeposited hydroxyapatite thin films modified by ion beam irradiation" in Journal of Optoelectronics and Advanced Materials, 11, no. 11 (2009):1848-1854,
https://hdl.handle.net/21.15107/rcub_vinar_3872 .
5

Electrochemical synthesis of nanosized monetite powder and its electrophoretic deposition on titanium

Djosic, M. S.; Mišković-Stanković, Vesna B.; Kačarević-Popović, Zorica M.; Jokić, Bojan M.; Bibić, Nataša M.; Mitrić, Miodrag; Milonjić, Slobodan K.; Jančić-Heinemann, Radmila; Stojanovic, J.

(2009)

TY  - JOUR
AU  - Djosic, M. S.
AU  - Mišković-Stanković, Vesna B.
AU  - Kačarević-Popović, Zorica M.
AU  - Jokić, Bojan M.
AU  - Bibić, Nataša M.
AU  - Mitrić, Miodrag
AU  - Milonjić, Slobodan K.
AU  - Jančić-Heinemann, Radmila
AU  - Stojanovic, J.
PY  - 2009
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/3713
AB  - Electrochemical synthesis of nanosized monetite powder was performed galvanostatically from homogeneous Solution of Na(2)H(2)EDTA center dot 2H(2)O, NaH2PO4 and CaCl2 at a concentration relationship Ca/EDTA/PO43- of 0.25/0.25/0.15 M at current density of 137 mA cm(-2) and pH value of 5.0. The synthesized monetite powder was characterized by X-ray diffraction, infrared spectroscopy, size distribution measurements, thermogravimetric and differential thermal analysis and scanning electron microscopy. Monetite powder was electrophoretically deposited on titanium from ethanol Suspension, using constant voltage method. The deposition was performed at constant voltage between 10 and 50 V and for a constant deposition time between 1 and 30 min. The influence of the applied voltage and deposition time on the mass and morphology of monetite deposits was investigated. It was shown that monetite deposits of the highest thickness and the lowest porosity can be formed at lower applied voltage (30 V) and for longer deposition time (20 min) and then converted to hydroxyapatite. (C) 2009 Elsevier B.V. All rights reserved.
T2  - Colloids and Surfaces. A: Physicochemical and Engineering Aspects
T1  - Electrochemical synthesis of nanosized monetite powder and its electrophoretic deposition on titanium
VL  - 341
IS  - 1-3
SP  - 110
EP  - 117
DO  - 10.1016/j.colsurfa.2009.03.046
ER  - 
@article{
author = "Djosic, M. S. and Mišković-Stanković, Vesna B. and Kačarević-Popović, Zorica M. and Jokić, Bojan M. and Bibić, Nataša M. and Mitrić, Miodrag and Milonjić, Slobodan K. and Jančić-Heinemann, Radmila and Stojanovic, J.",
year = "2009",
abstract = "Electrochemical synthesis of nanosized monetite powder was performed galvanostatically from homogeneous Solution of Na(2)H(2)EDTA center dot 2H(2)O, NaH2PO4 and CaCl2 at a concentration relationship Ca/EDTA/PO43- of 0.25/0.25/0.15 M at current density of 137 mA cm(-2) and pH value of 5.0. The synthesized monetite powder was characterized by X-ray diffraction, infrared spectroscopy, size distribution measurements, thermogravimetric and differential thermal analysis and scanning electron microscopy. Monetite powder was electrophoretically deposited on titanium from ethanol Suspension, using constant voltage method. The deposition was performed at constant voltage between 10 and 50 V and for a constant deposition time between 1 and 30 min. The influence of the applied voltage and deposition time on the mass and morphology of monetite deposits was investigated. It was shown that monetite deposits of the highest thickness and the lowest porosity can be formed at lower applied voltage (30 V) and for longer deposition time (20 min) and then converted to hydroxyapatite. (C) 2009 Elsevier B.V. All rights reserved.",
journal = "Colloids and Surfaces. A: Physicochemical and Engineering Aspects",
title = "Electrochemical synthesis of nanosized monetite powder and its electrophoretic deposition on titanium",
volume = "341",
number = "1-3",
pages = "110-117",
doi = "10.1016/j.colsurfa.2009.03.046"
}
Djosic, M. S., Mišković-Stanković, V. B., Kačarević-Popović, Z. M., Jokić, B. M., Bibić, N. M., Mitrić, M., Milonjić, S. K., Jančić-Heinemann, R.,& Stojanovic, J.. (2009). Electrochemical synthesis of nanosized monetite powder and its electrophoretic deposition on titanium. in Colloids and Surfaces. A: Physicochemical and Engineering Aspects, 341(1-3), 110-117.
https://doi.org/10.1016/j.colsurfa.2009.03.046
Djosic MS, Mišković-Stanković VB, Kačarević-Popović ZM, Jokić BM, Bibić NM, Mitrić M, Milonjić SK, Jančić-Heinemann R, Stojanovic J. Electrochemical synthesis of nanosized monetite powder and its electrophoretic deposition on titanium. in Colloids and Surfaces. A: Physicochemical and Engineering Aspects. 2009;341(1-3):110-117.
doi:10.1016/j.colsurfa.2009.03.046 .
Djosic, M. S., Mišković-Stanković, Vesna B., Kačarević-Popović, Zorica M., Jokić, Bojan M., Bibić, Nataša M., Mitrić, Miodrag, Milonjić, Slobodan K., Jančić-Heinemann, Radmila, Stojanovic, J., "Electrochemical synthesis of nanosized monetite powder and its electrophoretic deposition on titanium" in Colloids and Surfaces. A: Physicochemical and Engineering Aspects, 341, no. 1-3 (2009):110-117,
https://doi.org/10.1016/j.colsurfa.2009.03.046 . .
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Electrochemical synthesis and characterization of hydroxyapatite powders

Djosic, M. S.; Mišković-Stanković, Vesna B.; Milonjić, Slobodan K.; Kačarević-Popović, Zorica M.; Bibić, Nataša M.; Stojanovic, J.

(2008)

TY  - JOUR
AU  - Djosic, M. S.
AU  - Mišković-Stanković, Vesna B.
AU  - Milonjić, Slobodan K.
AU  - Kačarević-Popović, Zorica M.
AU  - Bibić, Nataša M.
AU  - Stojanovic, J.
PY  - 2008
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/3487
AB  - Electrochemical synthesis of hydroxyapatite powders was performed galvanostatically from homogeneous solution of Na(2)H(2)EDTA center dot 2H(2)O, NaH2PO4 and CaCl2 at a concentration relationship Ca/EDTA/PO43- of 0.25/0.25/0.15 M at current densities of 137 and 207 mA cm(-2) and pH values of 9.0 and 12.0. The hydroxyapatite powders were characterized by X-ray diffraction, size distribution measurements, transmission electron microscopy, scanning electron microscopy and thermogravimetric and differential thermal analysis. The influence of the electrochemical synthesis parameters, e.g. applied current density and pH value, on the phase composition, crystallite size, morphology and thermal characteristics of hydroxyapatite powders were investigated. (c) 2008 Elsevier B.V. All rights reserved.
T2  - Materials Chemistry and Physics
T1  - Electrochemical synthesis and characterization of hydroxyapatite powders
VL  - 111
IS  - 1
SP  - 137
EP  - 142
DO  - 10.1016/j.matchemphys.2008.03.045
ER  - 
@article{
author = "Djosic, M. S. and Mišković-Stanković, Vesna B. and Milonjić, Slobodan K. and Kačarević-Popović, Zorica M. and Bibić, Nataša M. and Stojanovic, J.",
year = "2008",
abstract = "Electrochemical synthesis of hydroxyapatite powders was performed galvanostatically from homogeneous solution of Na(2)H(2)EDTA center dot 2H(2)O, NaH2PO4 and CaCl2 at a concentration relationship Ca/EDTA/PO43- of 0.25/0.25/0.15 M at current densities of 137 and 207 mA cm(-2) and pH values of 9.0 and 12.0. The hydroxyapatite powders were characterized by X-ray diffraction, size distribution measurements, transmission electron microscopy, scanning electron microscopy and thermogravimetric and differential thermal analysis. The influence of the electrochemical synthesis parameters, e.g. applied current density and pH value, on the phase composition, crystallite size, morphology and thermal characteristics of hydroxyapatite powders were investigated. (c) 2008 Elsevier B.V. All rights reserved.",
journal = "Materials Chemistry and Physics",
title = "Electrochemical synthesis and characterization of hydroxyapatite powders",
volume = "111",
number = "1",
pages = "137-142",
doi = "10.1016/j.matchemphys.2008.03.045"
}
Djosic, M. S., Mišković-Stanković, V. B., Milonjić, S. K., Kačarević-Popović, Z. M., Bibić, N. M.,& Stojanovic, J.. (2008). Electrochemical synthesis and characterization of hydroxyapatite powders. in Materials Chemistry and Physics, 111(1), 137-142.
https://doi.org/10.1016/j.matchemphys.2008.03.045
Djosic MS, Mišković-Stanković VB, Milonjić SK, Kačarević-Popović ZM, Bibić NM, Stojanovic J. Electrochemical synthesis and characterization of hydroxyapatite powders. in Materials Chemistry and Physics. 2008;111(1):137-142.
doi:10.1016/j.matchemphys.2008.03.045 .
Djosic, M. S., Mišković-Stanković, Vesna B., Milonjić, Slobodan K., Kačarević-Popović, Zorica M., Bibić, Nataša M., Stojanovic, J., "Electrochemical synthesis and characterization of hydroxyapatite powders" in Materials Chemistry and Physics, 111, no. 1 (2008):137-142,
https://doi.org/10.1016/j.matchemphys.2008.03.045 . .
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