Stojanović, Jovica

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Authority KeyName Variants
0ed7fda9-1625-44f0-8ab9-f2d35b323c26
  • Stojanović, Jovica (27)
Projects
The development of glasses with controlled ions release for application in agriculture and medicine Phenomena and processes of the synthesis of new glassy and nano-structured glass-ceramics materials
Synthesis, processing and applications of nanostructured multifunctional materials with defined properties Basic Science Research Program of the Ministry of Education, Science and Technology of Korea [2018R1A2B5A02023190]
Developing technological processes for nonstandard copper concentrates processing with the aim to decrease pollutants emission Elektrohemijske karakteristike oksidnih i polimernih prevlaka na modifikovanim površinama metala
Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200135 (University of Belgrade, Faculty of Technology and Metallurgy) Implementation of new technical, technological and environmental solutions in the mining and metallurgical operations RBB and RBM
Basic Science Research Program through National Research Foundation of Korea (NRF) - Ministry of Education, Science and Technology [2016R1A2B4016034] Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200023 (Institute of Technology of Nuclear and Other Mineral Row Materials - ITNMS, Belgrade)
Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200287 (Innovation Center of the Faculty of Technology and Metallurgy) Novel encapsulation and enzyme technologies for designing of new biocatalysts and biologically active compounds targeting enhancement of food quality, safety and competitiveness
Modifikacija, sinteza i analiza nanostrukturnih materijala jonskim snopovima, gama zračenjem i vakuumskim deponovanjem Sinteza, karakterizacija i primena koloidnih disperzija neorganskih materijala nanometarskih veličina
Sinteza, struktura, svojstva i primena funkcionalnih nanostrukturnih keramičkih i biokeramičkih materijala The development of casting technologies under the influence of electromagnetic field and technologies of hot plastic forming of 7000 series aluminium alloys for special purposes
Innovative synergy of by-products, waste minimization and clean technologies in metallurgy

Author's Bibliography

Antibacterial graphene-based hydroxyapatite/chitosan coating with gentamicin for potential applications in bone tissue engineering

Stevanović, Milena; Đošić, Marija; Janković, Ana; Kojić, Vesna; Vukašinović-Sekulić, Maja; Stojanović, Jovica; Odović, Jadranka; Crevar-Sakač, Milkica; Kyong Yop, Rhee; Mišković-Stanković, Vesna

(Wiley, Hoboken, 2020)

TY  - JOUR
AU  - Stevanović, Milena
AU  - Đošić, Marija
AU  - Janković, Ana
AU  - Kojić, Vesna
AU  - Vukašinović-Sekulić, Maja
AU  - Stojanović, Jovica
AU  - Odović, Jadranka
AU  - Crevar-Sakač, Milkica
AU  - Kyong Yop, Rhee
AU  - Mišković-Stanković, Vesna
PY  - 2020
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4501
AB  - Electrophoretic deposition process (EPD) was successfully used for obtaining graphene (Gr)-reinforced composite coating based on hydroxyapatite (HAP), chitosan (CS), and antibiotic gentamicin (Gent), from aqueous suspension. The deposition process was performed as a single step process at a constant voltage (5 V, deposition time 12 min) on pure titanium foils. The influence of graphene was examined through detailed physicochemical and biological characterization. Fourier transform infrared spectroscopy, field emission scanning electron microscopy, thermogravimetric analysis, X-ray diffraction, Raman, and X-ray photoelectron analyses confirmed the formation of composite HAP/CS/Gr and HAP/CS/Gr/Gent coatings on Ti. Obtained coatings had porous, uniform, fracture-free surfaces, suggesting strong interfacial interaction between HAP, CS, and Gr. Large specific area of graphene enabled strong bonding with chitosan, acting as nanofiller throughout the polymer matrix. Gentamicin addition strongly improved the antibacterial activity of HAP/CS/Gr/Gent coating that was confirmed by antibacterial activity kinetics in suspension and agar diffusion testing, while results indicated more pronounced antibacterial effect againstStaphylococcus aureus(bactericidal, viable cells number reduction  gt 3 logarithmic units) compared toEscherichia coli(bacteriostatic, lt 3 logarithmic units).MTT assay indicated low cytotoxicity (75% cell viability) against MRC-5 and L929 (70% cell viability) tested cell lines, indicating good biocompatibility of HAP/CS/Gr/Gent coating. Therefore, electrodeposited HAP/CS/Gr/Gent coating on Ti can be considered as a prospective material for bone tissue engineering as a hard tissue implant.
PB  - Wiley, Hoboken
T2  - Journal of Biomedical Materials Research Part A
T1  - Antibacterial graphene-based hydroxyapatite/chitosan coating with gentamicin for potential applications in bone tissue engineering
EP  - 2189
IS  - 11
SP  - 2175
VL  - 108
DO  - 10.1002/jbm.a.36974
ER  - 
@article{
author = "Stevanović, Milena and Đošić, Marija and Janković, Ana and Kojić, Vesna and Vukašinović-Sekulić, Maja and Stojanović, Jovica and Odović, Jadranka and Crevar-Sakač, Milkica and Kyong Yop, Rhee and Mišković-Stanković, Vesna",
year = "2020",
abstract = "Electrophoretic deposition process (EPD) was successfully used for obtaining graphene (Gr)-reinforced composite coating based on hydroxyapatite (HAP), chitosan (CS), and antibiotic gentamicin (Gent), from aqueous suspension. The deposition process was performed as a single step process at a constant voltage (5 V, deposition time 12 min) on pure titanium foils. The influence of graphene was examined through detailed physicochemical and biological characterization. Fourier transform infrared spectroscopy, field emission scanning electron microscopy, thermogravimetric analysis, X-ray diffraction, Raman, and X-ray photoelectron analyses confirmed the formation of composite HAP/CS/Gr and HAP/CS/Gr/Gent coatings on Ti. Obtained coatings had porous, uniform, fracture-free surfaces, suggesting strong interfacial interaction between HAP, CS, and Gr. Large specific area of graphene enabled strong bonding with chitosan, acting as nanofiller throughout the polymer matrix. Gentamicin addition strongly improved the antibacterial activity of HAP/CS/Gr/Gent coating that was confirmed by antibacterial activity kinetics in suspension and agar diffusion testing, while results indicated more pronounced antibacterial effect againstStaphylococcus aureus(bactericidal, viable cells number reduction  gt 3 logarithmic units) compared toEscherichia coli(bacteriostatic, lt 3 logarithmic units).MTT assay indicated low cytotoxicity (75% cell viability) against MRC-5 and L929 (70% cell viability) tested cell lines, indicating good biocompatibility of HAP/CS/Gr/Gent coating. Therefore, electrodeposited HAP/CS/Gr/Gent coating on Ti can be considered as a prospective material for bone tissue engineering as a hard tissue implant.",
publisher = "Wiley, Hoboken",
journal = "Journal of Biomedical Materials Research Part A",
title = "Antibacterial graphene-based hydroxyapatite/chitosan coating with gentamicin for potential applications in bone tissue engineering",
pages = "2189-2175",
number = "11",
volume = "108",
doi = "10.1002/jbm.a.36974"
}
Stevanović, M., Đošić, M., Janković, A., Kojić, V., Vukašinović-Sekulić, M., Stojanović, J., Odović, J., Crevar-Sakač, M., Kyong Yop, R.,& Mišković-Stanković, V.. (2020). Antibacterial graphene-based hydroxyapatite/chitosan coating with gentamicin for potential applications in bone tissue engineering. in Journal of Biomedical Materials Research Part A
Wiley, Hoboken., 108(11), 2175-2189.
https://doi.org/10.1002/jbm.a.36974
Stevanović M, Đošić M, Janković A, Kojić V, Vukašinović-Sekulić M, Stojanović J, Odović J, Crevar-Sakač M, Kyong Yop R, Mišković-Stanković V. Antibacterial graphene-based hydroxyapatite/chitosan coating with gentamicin for potential applications in bone tissue engineering. in Journal of Biomedical Materials Research Part A. 2020;108(11):2175-2189.
doi:10.1002/jbm.a.36974 .
Stevanović, Milena, Đošić, Marija, Janković, Ana, Kojić, Vesna, Vukašinović-Sekulić, Maja, Stojanović, Jovica, Odović, Jadranka, Crevar-Sakač, Milkica, Kyong Yop, Rhee, Mišković-Stanković, Vesna, "Antibacterial graphene-based hydroxyapatite/chitosan coating with gentamicin for potential applications in bone tissue engineering" in Journal of Biomedical Materials Research Part A, 108, no. 11 (2020):2175-2189,
https://doi.org/10.1002/jbm.a.36974 . .
43
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41

Antibacterial graphene-based hydroxyapatite/chitosan coating with gentamicin for potential applications in bone tissue engineering

Stevanović, Milena; Đošić, Marija; Janković, Ana; Kojić, Vesna; Vukašinović-Sekulić, Maja; Stojanović, Jovica; Odović, Jadranka; Crevar-Sakač, Milkica; Kyong Yop, Rhee; Mišković-Stanković, Vesna

(Wiley, Hoboken, 2020)

TY  - JOUR
AU  - Stevanović, Milena
AU  - Đošić, Marija
AU  - Janković, Ana
AU  - Kojić, Vesna
AU  - Vukašinović-Sekulić, Maja
AU  - Stojanović, Jovica
AU  - Odović, Jadranka
AU  - Crevar-Sakač, Milkica
AU  - Kyong Yop, Rhee
AU  - Mišković-Stanković, Vesna
PY  - 2020
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4725
AB  - Electrophoretic deposition process (EPD) was successfully used for obtaining graphene (Gr)-reinforced composite coating based on hydroxyapatite (HAP), chitosan (CS), and antibiotic gentamicin (Gent), from aqueous suspension. The deposition process was performed as a single step process at a constant voltage (5 V, deposition time 12 min) on pure titanium foils. The influence of graphene was examined through detailed physicochemical and biological characterization. Fourier transform infrared spectroscopy, field emission scanning electron microscopy, thermogravimetric analysis, X-ray diffraction, Raman, and X-ray photoelectron analyses confirmed the formation of composite HAP/CS/Gr and HAP/CS/Gr/Gent coatings on Ti. Obtained coatings had porous, uniform, fracture-free surfaces, suggesting strong interfacial interaction between HAP, CS, and Gr. Large specific area of graphene enabled strong bonding with chitosan, acting as nanofiller throughout the polymer matrix. Gentamicin addition strongly improved the antibacterial activity of HAP/CS/Gr/Gent coating that was confirmed by antibacterial activity kinetics in suspension and agar diffusion testing, while results indicated more pronounced antibacterial effect againstStaphylococcus aureus(bactericidal, viable cells number reduction  gt 3 logarithmic units) compared toEscherichia coli(bacteriostatic, lt 3 logarithmic units).MTT assay indicated low cytotoxicity (75% cell viability) against MRC-5 and L929 (70% cell viability) tested cell lines, indicating good biocompatibility of HAP/CS/Gr/Gent coating. Therefore, electrodeposited HAP/CS/Gr/Gent coating on Ti can be considered as a prospective material for bone tissue engineering as a hard tissue implant.
PB  - Wiley, Hoboken
T2  - Journal of Biomedical Materials Research Part A
T1  - Antibacterial graphene-based hydroxyapatite/chitosan coating with gentamicin for potential applications in bone tissue engineering
EP  - 2189
IS  - 11
SP  - 2175
VL  - 108
DO  - 10.1002/jbm.a.36974
ER  - 
@article{
author = "Stevanović, Milena and Đošić, Marija and Janković, Ana and Kojić, Vesna and Vukašinović-Sekulić, Maja and Stojanović, Jovica and Odović, Jadranka and Crevar-Sakač, Milkica and Kyong Yop, Rhee and Mišković-Stanković, Vesna",
year = "2020",
abstract = "Electrophoretic deposition process (EPD) was successfully used for obtaining graphene (Gr)-reinforced composite coating based on hydroxyapatite (HAP), chitosan (CS), and antibiotic gentamicin (Gent), from aqueous suspension. The deposition process was performed as a single step process at a constant voltage (5 V, deposition time 12 min) on pure titanium foils. The influence of graphene was examined through detailed physicochemical and biological characterization. Fourier transform infrared spectroscopy, field emission scanning electron microscopy, thermogravimetric analysis, X-ray diffraction, Raman, and X-ray photoelectron analyses confirmed the formation of composite HAP/CS/Gr and HAP/CS/Gr/Gent coatings on Ti. Obtained coatings had porous, uniform, fracture-free surfaces, suggesting strong interfacial interaction between HAP, CS, and Gr. Large specific area of graphene enabled strong bonding with chitosan, acting as nanofiller throughout the polymer matrix. Gentamicin addition strongly improved the antibacterial activity of HAP/CS/Gr/Gent coating that was confirmed by antibacterial activity kinetics in suspension and agar diffusion testing, while results indicated more pronounced antibacterial effect againstStaphylococcus aureus(bactericidal, viable cells number reduction  gt 3 logarithmic units) compared toEscherichia coli(bacteriostatic, lt 3 logarithmic units).MTT assay indicated low cytotoxicity (75% cell viability) against MRC-5 and L929 (70% cell viability) tested cell lines, indicating good biocompatibility of HAP/CS/Gr/Gent coating. Therefore, electrodeposited HAP/CS/Gr/Gent coating on Ti can be considered as a prospective material for bone tissue engineering as a hard tissue implant.",
publisher = "Wiley, Hoboken",
journal = "Journal of Biomedical Materials Research Part A",
title = "Antibacterial graphene-based hydroxyapatite/chitosan coating with gentamicin for potential applications in bone tissue engineering",
pages = "2189-2175",
number = "11",
volume = "108",
doi = "10.1002/jbm.a.36974"
}
Stevanović, M., Đošić, M., Janković, A., Kojić, V., Vukašinović-Sekulić, M., Stojanović, J., Odović, J., Crevar-Sakač, M., Kyong Yop, R.,& Mišković-Stanković, V.. (2020). Antibacterial graphene-based hydroxyapatite/chitosan coating with gentamicin for potential applications in bone tissue engineering. in Journal of Biomedical Materials Research Part A
Wiley, Hoboken., 108(11), 2175-2189.
https://doi.org/10.1002/jbm.a.36974
Stevanović M, Đošić M, Janković A, Kojić V, Vukašinović-Sekulić M, Stojanović J, Odović J, Crevar-Sakač M, Kyong Yop R, Mišković-Stanković V. Antibacterial graphene-based hydroxyapatite/chitosan coating with gentamicin for potential applications in bone tissue engineering. in Journal of Biomedical Materials Research Part A. 2020;108(11):2175-2189.
doi:10.1002/jbm.a.36974 .
Stevanović, Milena, Đošić, Marija, Janković, Ana, Kojić, Vesna, Vukašinović-Sekulić, Maja, Stojanović, Jovica, Odović, Jadranka, Crevar-Sakač, Milkica, Kyong Yop, Rhee, Mišković-Stanković, Vesna, "Antibacterial graphene-based hydroxyapatite/chitosan coating with gentamicin for potential applications in bone tissue engineering" in Journal of Biomedical Materials Research Part A, 108, no. 11 (2020):2175-2189,
https://doi.org/10.1002/jbm.a.36974 . .
43
14
44

Assessing the Bioactivity of Gentamicin-Preloaded Hydroxyapatite/Chitosan Composite Coating on Titanium Substrate

Stevanović, Milena; Đošić, Marija; Janković, Ana; Nešović, Katarina; Kojić, Vesna; Stojanović, Jovica; Grujić, Svetlana; Matić-Bujagić, Ivana; Rhee, Kyong Yop; Mišković-Stanković, Vesna

(Amer Chemical Soc, Washington, 2020)

TY  - JOUR
AU  - Stevanović, Milena
AU  - Đošić, Marija
AU  - Janković, Ana
AU  - Nešović, Katarina
AU  - Kojić, Vesna
AU  - Stojanović, Jovica
AU  - Grujić, Svetlana
AU  - Matić-Bujagić, Ivana
AU  - Rhee, Kyong Yop
AU  - Mišković-Stanković, Vesna
PY  - 2020
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4498
AB  - The electrophoretic deposition process (EPD) was utilized to produce bioactive hydroxyapatite/chitosan (HAP/CS) and hydroxyapatite/chitosan/gentamicin (HAP/CS/Gent) coatings on titanium. The bioactivity of newly synthesized composite coatings was investigated in the simulated body fluid (SBF) and examined by X-ray diffraction, Fourier transform infrared spectroscopy, and field emission scanning electron microscopy. The obtained results revealed carbonate-substituted hydroxyapatite after immersion in SBF, emphasizing the similarity of the biomimetically grown HAP with the naturally occurring apatite in the bone. The formation of biomimetic HAP was confirmed by electrochemical impedance spectroscopy and polarization measurements, through the decrease in corrosion current density and coating capacitance values after 28-day immersion in SBF. The osseointegration ability was further validated by measuring the alkaline phosphatase activity (ALP) indicating the favorable osseopromotive properties of deposited coatings (significant increase in ALP levels for both HAP/CS (3.206 U mL(-1)) and HAP/CS/Gent (4.039 U mL(-1)) coatings, compared to the control (0.900 U mL(-1))). Drug-release kinetics was investigated in deionized water at 37 degrees C by high-performance liquid chromatography coupled with mass spectrometry. Release profiles revealed the beneficial "burst-release effect" (similar to 21% of gentamicin released in the first 48 h) as a potentially promising solution against the biofilm formation in the initial period. When tested against human and mice fibroblast cells (MRC-5 and L929), both composite coatings showed a noncytotoxic effect (viability  gt 85%), providing a promising basis for further medical application trials.
PB  - Amer Chemical Soc, Washington
T2  - ACS Omega
T1  - Assessing the Bioactivity of Gentamicin-Preloaded Hydroxyapatite/Chitosan Composite Coating on Titanium Substrate
EP  - 15445
IS  - 25
SP  - 15433
VL  - 5
DO  - 10.1021/acsomega.0c01583
ER  - 
@article{
author = "Stevanović, Milena and Đošić, Marija and Janković, Ana and Nešović, Katarina and Kojić, Vesna and Stojanović, Jovica and Grujić, Svetlana and Matić-Bujagić, Ivana and Rhee, Kyong Yop and Mišković-Stanković, Vesna",
year = "2020",
abstract = "The electrophoretic deposition process (EPD) was utilized to produce bioactive hydroxyapatite/chitosan (HAP/CS) and hydroxyapatite/chitosan/gentamicin (HAP/CS/Gent) coatings on titanium. The bioactivity of newly synthesized composite coatings was investigated in the simulated body fluid (SBF) and examined by X-ray diffraction, Fourier transform infrared spectroscopy, and field emission scanning electron microscopy. The obtained results revealed carbonate-substituted hydroxyapatite after immersion in SBF, emphasizing the similarity of the biomimetically grown HAP with the naturally occurring apatite in the bone. The formation of biomimetic HAP was confirmed by electrochemical impedance spectroscopy and polarization measurements, through the decrease in corrosion current density and coating capacitance values after 28-day immersion in SBF. The osseointegration ability was further validated by measuring the alkaline phosphatase activity (ALP) indicating the favorable osseopromotive properties of deposited coatings (significant increase in ALP levels for both HAP/CS (3.206 U mL(-1)) and HAP/CS/Gent (4.039 U mL(-1)) coatings, compared to the control (0.900 U mL(-1))). Drug-release kinetics was investigated in deionized water at 37 degrees C by high-performance liquid chromatography coupled with mass spectrometry. Release profiles revealed the beneficial "burst-release effect" (similar to 21% of gentamicin released in the first 48 h) as a potentially promising solution against the biofilm formation in the initial period. When tested against human and mice fibroblast cells (MRC-5 and L929), both composite coatings showed a noncytotoxic effect (viability  gt 85%), providing a promising basis for further medical application trials.",
publisher = "Amer Chemical Soc, Washington",
journal = "ACS Omega",
title = "Assessing the Bioactivity of Gentamicin-Preloaded Hydroxyapatite/Chitosan Composite Coating on Titanium Substrate",
pages = "15445-15433",
number = "25",
volume = "5",
doi = "10.1021/acsomega.0c01583"
}
Stevanović, M., Đošić, M., Janković, A., Nešović, K., Kojić, V., Stojanović, J., Grujić, S., Matić-Bujagić, I., Rhee, K. Y.,& Mišković-Stanković, V.. (2020). Assessing the Bioactivity of Gentamicin-Preloaded Hydroxyapatite/Chitosan Composite Coating on Titanium Substrate. in ACS Omega
Amer Chemical Soc, Washington., 5(25), 15433-15445.
https://doi.org/10.1021/acsomega.0c01583
Stevanović M, Đošić M, Janković A, Nešović K, Kojić V, Stojanović J, Grujić S, Matić-Bujagić I, Rhee KY, Mišković-Stanković V. Assessing the Bioactivity of Gentamicin-Preloaded Hydroxyapatite/Chitosan Composite Coating on Titanium Substrate. in ACS Omega. 2020;5(25):15433-15445.
doi:10.1021/acsomega.0c01583 .
Stevanović, Milena, Đošić, Marija, Janković, Ana, Nešović, Katarina, Kojić, Vesna, Stojanović, Jovica, Grujić, Svetlana, Matić-Bujagić, Ivana, Rhee, Kyong Yop, Mišković-Stanković, Vesna, "Assessing the Bioactivity of Gentamicin-Preloaded Hydroxyapatite/Chitosan Composite Coating on Titanium Substrate" in ACS Omega, 5, no. 25 (2020):15433-15445,
https://doi.org/10.1021/acsomega.0c01583 . .
30
9
29

Crystal growth of la(2)srb(10)o(19)from undercooled melt

Smiljanić, Sonja; Grujić, Snežana; Matijašević, Srđan D.; Stojanović, Jovica; Nikolić, Jelena; Savić, Veljko; Popović, Daniela

(Springer, Dordrecht, 2020)

TY  - JOUR
AU  - Smiljanić, Sonja
AU  - Grujić, Snežana
AU  - Matijašević, Srđan D.
AU  - Stojanović, Jovica
AU  - Nikolić, Jelena
AU  - Savić, Veljko
AU  - Popović, Daniela
PY  - 2020
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/13
AB  - The crystal growth rate of La(2)SrB(10)O(19)in an undercooled melt of stoichiometric composition was studied. The crystallization of the bulk samples was performed in a single-stage regime under isothermal conditions at the selected temperatures for the different time periods. The surface crystallization was observed and in all crystallized samples, the La(2)SrB(10)O(19)crystalline phase was identified. Based on the dependence of the crystalline layer thickness on treatment time at selected temperature, crystal growth rate was obtained. The crystal growth rates were from 1.65 x 10(-8)to 2.77 x 10(-7)m s(-1)in the temperature interval (700-780 degrees C). The experimental values were compared to the calculated values using theoretical model of the crystal growth. The experimental growth rate followed the same trend as the calculated growth rate, but the experimental values were higher than the calculated.
PB  - Springer, Dordrecht
T2  - Journal of Thermal Analysis and Calorimetry
T1  - Crystal growth of la(2)srb(10)o(19)from undercooled melt
DO  - 10.1007/s10973-020-10122-1
ER  - 
@article{
author = "Smiljanić, Sonja and Grujić, Snežana and Matijašević, Srđan D. and Stojanović, Jovica and Nikolić, Jelena and Savić, Veljko and Popović, Daniela",
year = "2020",
abstract = "The crystal growth rate of La(2)SrB(10)O(19)in an undercooled melt of stoichiometric composition was studied. The crystallization of the bulk samples was performed in a single-stage regime under isothermal conditions at the selected temperatures for the different time periods. The surface crystallization was observed and in all crystallized samples, the La(2)SrB(10)O(19)crystalline phase was identified. Based on the dependence of the crystalline layer thickness on treatment time at selected temperature, crystal growth rate was obtained. The crystal growth rates were from 1.65 x 10(-8)to 2.77 x 10(-7)m s(-1)in the temperature interval (700-780 degrees C). The experimental values were compared to the calculated values using theoretical model of the crystal growth. The experimental growth rate followed the same trend as the calculated growth rate, but the experimental values were higher than the calculated.",
publisher = "Springer, Dordrecht",
journal = "Journal of Thermal Analysis and Calorimetry",
title = "Crystal growth of la(2)srb(10)o(19)from undercooled melt",
doi = "10.1007/s10973-020-10122-1"
}
Smiljanić, S., Grujić, S., Matijašević, S. D., Stojanović, J., Nikolić, J., Savić, V.,& Popović, D.. (2020). Crystal growth of la(2)srb(10)o(19)from undercooled melt. in Journal of Thermal Analysis and Calorimetry
Springer, Dordrecht..
https://doi.org/10.1007/s10973-020-10122-1
Smiljanić S, Grujić S, Matijašević SD, Stojanović J, Nikolić J, Savić V, Popović D. Crystal growth of la(2)srb(10)o(19)from undercooled melt. in Journal of Thermal Analysis and Calorimetry. 2020;.
doi:10.1007/s10973-020-10122-1 .
Smiljanić, Sonja, Grujić, Snežana, Matijašević, Srđan D., Stojanović, Jovica, Nikolić, Jelena, Savić, Veljko, Popović, Daniela, "Crystal growth of la(2)srb(10)o(19)from undercooled melt" in Journal of Thermal Analysis and Calorimetry (2020),
https://doi.org/10.1007/s10973-020-10122-1 . .
2
1

Treatment of the acidic effluent from a copper smelter by flotation tailings

Sokić, Miroslav; Radovanović, Dragana; Marković, Branislav; Stojanović, Jovica; Kamberović, Željko; Petronijević, Nela; Stanković, Srđan

(Savez hemijskih inženjera, Beograd, 2019)

TY  - JOUR
AU  - Sokić, Miroslav
AU  - Radovanović, Dragana
AU  - Marković, Branislav
AU  - Stojanović, Jovica
AU  - Kamberović, Željko
AU  - Petronijević, Nela
AU  - Stanković, Srđan
PY  - 2019
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4268
AB  - Since commissioning in 1961, the copper mine Majdanpek, a part of the Mining and Smelting Complex Bor (RTB Bor), produced approximately 378 million tons of flotation tailings. Semiquantitative mineralogical analysis of the flotation tailings revealed significant content of carbonate minerals (approximately 20-25 %), indicating high acid neutralization capacity. Also, approximately 70 % of copper is in the form of the oxide mineral cuprite (Cu2O). Copper can be easily leached from cuprite by using sulphuric acid. The RTB Bor copper smelter generates 8.7 m(3)h(-1) of extremely acidic waste effluent (142.4 kgm(-3) of sulphuric acid, pH - 0.464) with relatively high concentrations of dissolved metals and metalloids (Cu, Fe, Zn, Pb and As). The effluent is currently treated with hydrated lime. The present study focused on application of flotation tailings as a neutralizing agent for acidic effluents. Laboratory experiments followed by computer simulation of the industrial process showed that 99% of the acid can be neutralized with flotation tailings in a series of six reactors resulting in the final copper concentration of 1.55 gL(-1). Benefits of the proposed process are: lower environmental impact of the process and reduced costs of neutralization of the acidic effluent from the copper smelter.
PB  - Savez hemijskih inženjera, Beograd
T2  - Hemijska industrija
T1  - Treatment of the acidic effluent from a copper smelter by flotation tailings
EP  - 124
IS  - 2
SP  - 115
VL  - 73
DO  - 10.2298/HEMIND181009010S
ER  - 
@article{
author = "Sokić, Miroslav and Radovanović, Dragana and Marković, Branislav and Stojanović, Jovica and Kamberović, Željko and Petronijević, Nela and Stanković, Srđan",
year = "2019",
abstract = "Since commissioning in 1961, the copper mine Majdanpek, a part of the Mining and Smelting Complex Bor (RTB Bor), produced approximately 378 million tons of flotation tailings. Semiquantitative mineralogical analysis of the flotation tailings revealed significant content of carbonate minerals (approximately 20-25 %), indicating high acid neutralization capacity. Also, approximately 70 % of copper is in the form of the oxide mineral cuprite (Cu2O). Copper can be easily leached from cuprite by using sulphuric acid. The RTB Bor copper smelter generates 8.7 m(3)h(-1) of extremely acidic waste effluent (142.4 kgm(-3) of sulphuric acid, pH - 0.464) with relatively high concentrations of dissolved metals and metalloids (Cu, Fe, Zn, Pb and As). The effluent is currently treated with hydrated lime. The present study focused on application of flotation tailings as a neutralizing agent for acidic effluents. Laboratory experiments followed by computer simulation of the industrial process showed that 99% of the acid can be neutralized with flotation tailings in a series of six reactors resulting in the final copper concentration of 1.55 gL(-1). Benefits of the proposed process are: lower environmental impact of the process and reduced costs of neutralization of the acidic effluent from the copper smelter.",
publisher = "Savez hemijskih inženjera, Beograd",
journal = "Hemijska industrija",
title = "Treatment of the acidic effluent from a copper smelter by flotation tailings",
pages = "124-115",
number = "2",
volume = "73",
doi = "10.2298/HEMIND181009010S"
}
Sokić, M., Radovanović, D., Marković, B., Stojanović, J., Kamberović, Ž., Petronijević, N.,& Stanković, S.. (2019). Treatment of the acidic effluent from a copper smelter by flotation tailings. in Hemijska industrija
Savez hemijskih inženjera, Beograd., 73(2), 115-124.
https://doi.org/10.2298/HEMIND181009010S
Sokić M, Radovanović D, Marković B, Stojanović J, Kamberović Ž, Petronijević N, Stanković S. Treatment of the acidic effluent from a copper smelter by flotation tailings. in Hemijska industrija. 2019;73(2):115-124.
doi:10.2298/HEMIND181009010S .
Sokić, Miroslav, Radovanović, Dragana, Marković, Branislav, Stojanović, Jovica, Kamberović, Željko, Petronijević, Nela, Stanković, Srđan, "Treatment of the acidic effluent from a copper smelter by flotation tailings" in Hemijska industrija, 73, no. 2 (2019):115-124,
https://doi.org/10.2298/HEMIND181009010S . .
3
1
3

Structure and Microstructure Characterization of the La2SrB10O19 Glass-ceramics

Stojanović, Jovica; Smiljanić, Sonja; Grujić, Snežana; Vulić, Predrag; Matijašević, Srđan D.; Nikolić, Jelena D.; Savić, Veljko

(Međunarodni Institut za nauku o sinterovanju, Beograd, 2019)

TY  - JOUR
AU  - Stojanović, Jovica
AU  - Smiljanić, Sonja
AU  - Grujić, Snežana
AU  - Vulić, Predrag
AU  - Matijašević, Srđan D.
AU  - Nikolić, Jelena D.
AU  - Savić, Veljko
PY  - 2019
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4305
AB  - The crystal structure of new lanthanum strontium borate glass-ceramics was refined by the Rietveld method. The results showed that La2SrB10O19 has the monoclinic crystal structure, space group C2 (No. 5) with a = 11.1170(6), b = 6.5667(3), c = 9.2363(3) angstrom,beta = 91.481 degrees, V = 674.04(7) angstrom(3), two formula units per unit-cell, and density 3.830 g cm(-3). The main building units of the crystal structure are BO4 tetrahedra and BO3 triangles. Clusters composed of [B5O12] form an infinite double layer running perpendicular to the c-axis. Lanthanum atoms, situated in [B5O12](n) layers, are coordinated with 10 oxygen atom in a form of LaO10 polyhedra, while Sr atoms, located between [B5O12](n) layers, are coordinated with 8 oxygen atoms in a form of SrO8 polyhedra. Microstructural measurements contain both crystallite domain sizes and microstrain calculations obtained by the Warren Averbach and the simplified integral-breadth methods.
PB  - Međunarodni Institut za nauku o sinterovanju, Beograd
T2  - Science of Sintering
T1  - Structure and Microstructure Characterization of the La2SrB10O19 Glass-ceramics
EP  - 399
IS  - 4
SP  - 389
VL  - 51
DO  - 10.2298/SOS1904389S
ER  - 
@article{
author = "Stojanović, Jovica and Smiljanić, Sonja and Grujić, Snežana and Vulić, Predrag and Matijašević, Srđan D. and Nikolić, Jelena D. and Savić, Veljko",
year = "2019",
abstract = "The crystal structure of new lanthanum strontium borate glass-ceramics was refined by the Rietveld method. The results showed that La2SrB10O19 has the monoclinic crystal structure, space group C2 (No. 5) with a = 11.1170(6), b = 6.5667(3), c = 9.2363(3) angstrom,beta = 91.481 degrees, V = 674.04(7) angstrom(3), two formula units per unit-cell, and density 3.830 g cm(-3). The main building units of the crystal structure are BO4 tetrahedra and BO3 triangles. Clusters composed of [B5O12] form an infinite double layer running perpendicular to the c-axis. Lanthanum atoms, situated in [B5O12](n) layers, are coordinated with 10 oxygen atom in a form of LaO10 polyhedra, while Sr atoms, located between [B5O12](n) layers, are coordinated with 8 oxygen atoms in a form of SrO8 polyhedra. Microstructural measurements contain both crystallite domain sizes and microstrain calculations obtained by the Warren Averbach and the simplified integral-breadth methods.",
publisher = "Međunarodni Institut za nauku o sinterovanju, Beograd",
journal = "Science of Sintering",
title = "Structure and Microstructure Characterization of the La2SrB10O19 Glass-ceramics",
pages = "399-389",
number = "4",
volume = "51",
doi = "10.2298/SOS1904389S"
}
Stojanović, J., Smiljanić, S., Grujić, S., Vulić, P., Matijašević, S. D., Nikolić, J. D.,& Savić, V.. (2019). Structure and Microstructure Characterization of the La2SrB10O19 Glass-ceramics. in Science of Sintering
Međunarodni Institut za nauku o sinterovanju, Beograd., 51(4), 389-399.
https://doi.org/10.2298/SOS1904389S
Stojanović J, Smiljanić S, Grujić S, Vulić P, Matijašević SD, Nikolić JD, Savić V. Structure and Microstructure Characterization of the La2SrB10O19 Glass-ceramics. in Science of Sintering. 2019;51(4):389-399.
doi:10.2298/SOS1904389S .
Stojanović, Jovica, Smiljanić, Sonja, Grujić, Snežana, Vulić, Predrag, Matijašević, Srđan D., Nikolić, Jelena D., Savić, Veljko, "Structure and Microstructure Characterization of the La2SrB10O19 Glass-ceramics" in Science of Sintering, 51, no. 4 (2019):389-399,
https://doi.org/10.2298/SOS1904389S . .
2
3

Gentamicin-Loaded Bioactive Hydroxyapatite/Chitosan Composite Coating Electrodeposited on Titanium

Stevanović, Milena; Đošić, Marija; Janković, Ana; Kojić, Vesna; Vukašinović-Sekulić, Maja; Stojanović, Jovica; Odović, Jadranka; Crevar-Sakač, Milkica; Rhee, Kyong Yop; Mišković-Stanković, Vesna

(Amer Chemical Soc, Washington, 2018)

TY  - JOUR
AU  - Stevanović, Milena
AU  - Đošić, Marija
AU  - Janković, Ana
AU  - Kojić, Vesna
AU  - Vukašinović-Sekulić, Maja
AU  - Stojanović, Jovica
AU  - Odović, Jadranka
AU  - Crevar-Sakač, Milkica
AU  - Rhee, Kyong Yop
AU  - Mišković-Stanković, Vesna
PY  - 2018
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3899
AB  - Composite coating of antibiotic gentamicin (Gent), natural polymer chitosan (CS), and hydroxyapatite (HAP) was successfully assessed by applying the electrophoretic deposition (EPD) technique. EPD was performed under optimized deposition conditions (5 V, 12 min) on pure titanium plates, to obtain HAP/CS and HAP/CS/Gent composite coatings in a single step from three-component aqueous suspension, with favorable antibacterial properties. Composite coatings were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy, Fourier transform infrared spectroscopy, thermogravimetric analysis, and X-ray photoelectron analysis, confirming the formation of composite HAP/CS and HAP/CS/Gent coatings on the titanium surface, which is due to intermolecular hydrogen bonds. Employing the XRD technique, HAP was detected by obtaining the characteristic diffraction maximums. Good antibacterial activity of the composite coating loaded with antibiotic (HAP/CS/Gent) was confirmed against Staphylococcus aureus and Escherichia coli, pointing to the high potential for bioapplication. Introduction of gentamicin in HAP/CS/Gent coating caused very mild cytotoxicity in the tested cell lines MRC-5 and L929. MTT testing was used to evaluate cell viability, and HAP/CS was classified as noncytotoxic.
PB  - Amer Chemical Soc, Washington
T2  - ACS Biomaterials Science & Engineering
T1  - Gentamicin-Loaded Bioactive Hydroxyapatite/Chitosan Composite Coating Electrodeposited on Titanium
EP  - 4007
IS  - 12
SP  - 3994
VL  - 4
DO  - 10.1021/acsbiomaterials.8b00859
ER  - 
@article{
author = "Stevanović, Milena and Đošić, Marija and Janković, Ana and Kojić, Vesna and Vukašinović-Sekulić, Maja and Stojanović, Jovica and Odović, Jadranka and Crevar-Sakač, Milkica and Rhee, Kyong Yop and Mišković-Stanković, Vesna",
year = "2018",
abstract = "Composite coating of antibiotic gentamicin (Gent), natural polymer chitosan (CS), and hydroxyapatite (HAP) was successfully assessed by applying the electrophoretic deposition (EPD) technique. EPD was performed under optimized deposition conditions (5 V, 12 min) on pure titanium plates, to obtain HAP/CS and HAP/CS/Gent composite coatings in a single step from three-component aqueous suspension, with favorable antibacterial properties. Composite coatings were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy, Fourier transform infrared spectroscopy, thermogravimetric analysis, and X-ray photoelectron analysis, confirming the formation of composite HAP/CS and HAP/CS/Gent coatings on the titanium surface, which is due to intermolecular hydrogen bonds. Employing the XRD technique, HAP was detected by obtaining the characteristic diffraction maximums. Good antibacterial activity of the composite coating loaded with antibiotic (HAP/CS/Gent) was confirmed against Staphylococcus aureus and Escherichia coli, pointing to the high potential for bioapplication. Introduction of gentamicin in HAP/CS/Gent coating caused very mild cytotoxicity in the tested cell lines MRC-5 and L929. MTT testing was used to evaluate cell viability, and HAP/CS was classified as noncytotoxic.",
publisher = "Amer Chemical Soc, Washington",
journal = "ACS Biomaterials Science & Engineering",
title = "Gentamicin-Loaded Bioactive Hydroxyapatite/Chitosan Composite Coating Electrodeposited on Titanium",
pages = "4007-3994",
number = "12",
volume = "4",
doi = "10.1021/acsbiomaterials.8b00859"
}
Stevanović, M., Đošić, M., Janković, A., Kojić, V., Vukašinović-Sekulić, M., Stojanović, J., Odović, J., Crevar-Sakač, M., Rhee, K. Y.,& Mišković-Stanković, V.. (2018). Gentamicin-Loaded Bioactive Hydroxyapatite/Chitosan Composite Coating Electrodeposited on Titanium. in ACS Biomaterials Science & Engineering
Amer Chemical Soc, Washington., 4(12), 3994-4007.
https://doi.org/10.1021/acsbiomaterials.8b00859
Stevanović M, Đošić M, Janković A, Kojić V, Vukašinović-Sekulić M, Stojanović J, Odović J, Crevar-Sakač M, Rhee KY, Mišković-Stanković V. Gentamicin-Loaded Bioactive Hydroxyapatite/Chitosan Composite Coating Electrodeposited on Titanium. in ACS Biomaterials Science & Engineering. 2018;4(12):3994-4007.
doi:10.1021/acsbiomaterials.8b00859 .
Stevanović, Milena, Đošić, Marija, Janković, Ana, Kojić, Vesna, Vukašinović-Sekulić, Maja, Stojanović, Jovica, Odović, Jadranka, Crevar-Sakač, Milkica, Rhee, Kyong Yop, Mišković-Stanković, Vesna, "Gentamicin-Loaded Bioactive Hydroxyapatite/Chitosan Composite Coating Electrodeposited on Titanium" in ACS Biomaterials Science & Engineering, 4, no. 12 (2018):3994-4007,
https://doi.org/10.1021/acsbiomaterials.8b00859 . .
59
34
65

Sintering, crystallization and foaming of La2O3 center dot SrO center dot 5B(2)O(3) glass powders - effect of the holding temperature and the heating rate

Smiljanić, Sonja; Karamanova, Emilia; Grujić, Snežana; Rogan, Jelena; Stojanović, Jovica; Matijašević, Srđan D.; Karamanov, Alexander

(Elsevier Science Bv, Amsterdam, 2018)

TY  - JOUR
AU  - Smiljanić, Sonja
AU  - Karamanova, Emilia
AU  - Grujić, Snežana
AU  - Rogan, Jelena
AU  - Stojanović, Jovica
AU  - Matijašević, Srđan D.
AU  - Karamanov, Alexander
PY  - 2018
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3989
AB  - The peculiarities of sinter-crystallization of La2O3 center dot SrO center dot 5B(2)O(3) fine glass powder (below 1 mu m) are investigated and discussed. The sintering was studied by contactless optical dilatometry and porosity measurements. The crystallization process was evaluated by differential scanning calorimetry (DSC) and the crystalline phase formation was analyzed by X-ray diffraction (XRD). Finally the microstructures of the samples sintered at different temperatures were observed by field emission scanning electron microscope (FESEM). The specific aim of this study was to highlight the influence of sintering temperature and heating rate on the densification process and the final structure of glass-ceramic samples. It was shown that zero water adsorption and minimum closed porosity of similar to 3% were obtained at heating rate of 2 degrees C/min and at about 1 h holding at 690 degrees C. The temperature increase accelerated intense foaming process that resulted in formation of total porosity of 35-45%. It was also demonstrated that the foaming depended on the heating rate: the higher the heating rate - the more intensive was the bloating. The observed foaming process was related to intensive crystallization and re-crystallization of La2O3 center dot SrO center dot 5B(2)O(3) crystal phase. The phase formation processes entirely completed after 30-60 min at 730-740 degrees C with the formation of intriguing and unusual crystal structures.
PB  - Elsevier Science Bv, Amsterdam
T2  - Journal of Non-Crystalline Solids
T1  - Sintering, crystallization and foaming of La2O3 center dot SrO center dot 5B(2)O(3) glass powders - effect of the holding temperature and the heating rate
EP  - 382
SP  - 375
VL  - 481
DO  - 10.1016/j.jnoncrysol.2017.11.009
ER  - 
@article{
author = "Smiljanić, Sonja and Karamanova, Emilia and Grujić, Snežana and Rogan, Jelena and Stojanović, Jovica and Matijašević, Srđan D. and Karamanov, Alexander",
year = "2018",
abstract = "The peculiarities of sinter-crystallization of La2O3 center dot SrO center dot 5B(2)O(3) fine glass powder (below 1 mu m) are investigated and discussed. The sintering was studied by contactless optical dilatometry and porosity measurements. The crystallization process was evaluated by differential scanning calorimetry (DSC) and the crystalline phase formation was analyzed by X-ray diffraction (XRD). Finally the microstructures of the samples sintered at different temperatures were observed by field emission scanning electron microscope (FESEM). The specific aim of this study was to highlight the influence of sintering temperature and heating rate on the densification process and the final structure of glass-ceramic samples. It was shown that zero water adsorption and minimum closed porosity of similar to 3% were obtained at heating rate of 2 degrees C/min and at about 1 h holding at 690 degrees C. The temperature increase accelerated intense foaming process that resulted in formation of total porosity of 35-45%. It was also demonstrated that the foaming depended on the heating rate: the higher the heating rate - the more intensive was the bloating. The observed foaming process was related to intensive crystallization and re-crystallization of La2O3 center dot SrO center dot 5B(2)O(3) crystal phase. The phase formation processes entirely completed after 30-60 min at 730-740 degrees C with the formation of intriguing and unusual crystal structures.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Journal of Non-Crystalline Solids",
title = "Sintering, crystallization and foaming of La2O3 center dot SrO center dot 5B(2)O(3) glass powders - effect of the holding temperature and the heating rate",
pages = "382-375",
volume = "481",
doi = "10.1016/j.jnoncrysol.2017.11.009"
}
Smiljanić, S., Karamanova, E., Grujić, S., Rogan, J., Stojanović, J., Matijašević, S. D.,& Karamanov, A.. (2018). Sintering, crystallization and foaming of La2O3 center dot SrO center dot 5B(2)O(3) glass powders - effect of the holding temperature and the heating rate. in Journal of Non-Crystalline Solids
Elsevier Science Bv, Amsterdam., 481, 375-382.
https://doi.org/10.1016/j.jnoncrysol.2017.11.009
Smiljanić S, Karamanova E, Grujić S, Rogan J, Stojanović J, Matijašević SD, Karamanov A. Sintering, crystallization and foaming of La2O3 center dot SrO center dot 5B(2)O(3) glass powders - effect of the holding temperature and the heating rate. in Journal of Non-Crystalline Solids. 2018;481:375-382.
doi:10.1016/j.jnoncrysol.2017.11.009 .
Smiljanić, Sonja, Karamanova, Emilia, Grujić, Snežana, Rogan, Jelena, Stojanović, Jovica, Matijašević, Srđan D., Karamanov, Alexander, "Sintering, crystallization and foaming of La2O3 center dot SrO center dot 5B(2)O(3) glass powders - effect of the holding temperature and the heating rate" in Journal of Non-Crystalline Solids, 481 (2018):375-382,
https://doi.org/10.1016/j.jnoncrysol.2017.11.009 . .
11
9
12

Application of raw volcanic rock found in etna valley as an adsorbent of chromates, arsenates and selenates

Bugarčić, Mladen; Milivojević, Milan; Marinković, Aleksandar; Marković, Branislav; Sokić, Miroslav; Petronijević, Nela; Stojanović, Jovica

(Savez inženjera metalurgije Srbije, Beograd, 2018)

TY  - JOUR
AU  - Bugarčić, Mladen
AU  - Milivojević, Milan
AU  - Marinković, Aleksandar
AU  - Marković, Branislav
AU  - Sokić, Miroslav
AU  - Petronijević, Nela
AU  - Stojanović, Jovica
PY  - 2018
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3882
AB  - This paper aims to determine the potential of volcanic rock found in Etna valley as an adsorbent of heavy metals in anionic form (chromates, arsenates, and selenates). Characterization of the volcanic rock was done with chemical methods (AAS, AES, gravimetric analysis, XRF), physicochemical methods (XRD, FTIR, SEM, DTA, DTG) and physical methods (porosity measurement, Microscopy in transmitted light). Also, equilibrium adsorption capacity was determined. All the results of adsorption capacity were satisfying considering the mineral composition, granulation, and porosity. The removal efficiency of chromates was the biggest (above 30 %) with adsorption capacity of 15.6 mg Cr g(-1). The lowest adsorption efficiency was with the selenates, approximately 18 %.
PB  - Savez inženjera metalurgije Srbije, Beograd
T2  - Metallurgical & Materials Engineering
T1  - Application of raw volcanic rock found in etna valley as an adsorbent of chromates, arsenates and selenates
EP  - 144
IS  - 2
SP  - 133
VL  - 24
DO  - 10.30544/366
ER  - 
@article{
author = "Bugarčić, Mladen and Milivojević, Milan and Marinković, Aleksandar and Marković, Branislav and Sokić, Miroslav and Petronijević, Nela and Stojanović, Jovica",
year = "2018",
abstract = "This paper aims to determine the potential of volcanic rock found in Etna valley as an adsorbent of heavy metals in anionic form (chromates, arsenates, and selenates). Characterization of the volcanic rock was done with chemical methods (AAS, AES, gravimetric analysis, XRF), physicochemical methods (XRD, FTIR, SEM, DTA, DTG) and physical methods (porosity measurement, Microscopy in transmitted light). Also, equilibrium adsorption capacity was determined. All the results of adsorption capacity were satisfying considering the mineral composition, granulation, and porosity. The removal efficiency of chromates was the biggest (above 30 %) with adsorption capacity of 15.6 mg Cr g(-1). The lowest adsorption efficiency was with the selenates, approximately 18 %.",
publisher = "Savez inženjera metalurgije Srbije, Beograd",
journal = "Metallurgical & Materials Engineering",
title = "Application of raw volcanic rock found in etna valley as an adsorbent of chromates, arsenates and selenates",
pages = "144-133",
number = "2",
volume = "24",
doi = "10.30544/366"
}
Bugarčić, M., Milivojević, M., Marinković, A., Marković, B., Sokić, M., Petronijević, N.,& Stojanović, J.. (2018). Application of raw volcanic rock found in etna valley as an adsorbent of chromates, arsenates and selenates. in Metallurgical & Materials Engineering
Savez inženjera metalurgije Srbije, Beograd., 24(2), 133-144.
https://doi.org/10.30544/366
Bugarčić M, Milivojević M, Marinković A, Marković B, Sokić M, Petronijević N, Stojanović J. Application of raw volcanic rock found in etna valley as an adsorbent of chromates, arsenates and selenates. in Metallurgical & Materials Engineering. 2018;24(2):133-144.
doi:10.30544/366 .
Bugarčić, Mladen, Milivojević, Milan, Marinković, Aleksandar, Marković, Branislav, Sokić, Miroslav, Petronijević, Nela, Stojanović, Jovica, "Application of raw volcanic rock found in etna valley as an adsorbent of chromates, arsenates and selenates" in Metallurgical & Materials Engineering, 24, no. 2 (2018):133-144,
https://doi.org/10.30544/366 . .
4
3

Differences in coating mechanism of structurally different aluminosilicates observed through the thermal analysis

Milicević, Sonja; Martinović, Sanja; Milosević, Vladan; Stojanović, Jovica; Povrenović, Dragan

(Springer, Dordrecht, 2018)

TY  - JOUR
AU  - Milicević, Sonja
AU  - Martinović, Sanja
AU  - Milosević, Vladan
AU  - Stojanović, Jovica
AU  - Povrenović, Dragan
PY  - 2018
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3944
AB  - Systematic modification of three structurally different minerals (zeolite, mica, and vermiculite) was carried out with the aim of determining the modification mechanism and exposing the hydrophobic surface that can be used as a sorbent for many organic compounds. Mechanism of modification with cationic surfactant depends strongly on the mineral type. In order to identify the influence of aluminosilicates structural differences on the modification process, adsorption experiments with organic matter and water vapor, supplemented with the DTA/TG analysis, were performed. The cation exchange capacity (CEC) value was 1454 gt 560 gt 28meqkg(-1) for zeolite (clinoptilolite), vermiculite, and mica (muscovite), respectively. Despite its CEC value, vermiculite adsorbed three times the amount of organic matter than did clinoptilolite due to the porous structure of zeolite, which acted to limit the adsorption only on the external exchangeable cations. If the loading amount is equal to the CEC or the external cation exchange capacity for clinoptilolite (ECEC approximate to 10% CEC), the monolayer will form while mineral surface will have hydrophobic character. Only one active center exists at the surface of the clinoptilolite that was identified by DTA curves with a sharp and defined peak around 300 degrees C and by the mass loss at the TG diagrams. Two significant and equal active centers were observed in vermiculite, one for the exchange of the surface cations and the other for the interlayer cations and H2O molecules. Muscovite CEC is negligible, and due to the absence of any other functional groups, the modification of this mineral was impossible.
PB  - Springer, Dordrecht
T2  - Journal of Thermal Analysis and Calorimetry
T1  - Differences in coating mechanism of structurally different aluminosilicates observed through the thermal analysis
EP  - 1019
IS  - 2
SP  - 1011
VL  - 134
DO  - 10.1007/s10973-018-7351-3
ER  - 
@article{
author = "Milicević, Sonja and Martinović, Sanja and Milosević, Vladan and Stojanović, Jovica and Povrenović, Dragan",
year = "2018",
abstract = "Systematic modification of three structurally different minerals (zeolite, mica, and vermiculite) was carried out with the aim of determining the modification mechanism and exposing the hydrophobic surface that can be used as a sorbent for many organic compounds. Mechanism of modification with cationic surfactant depends strongly on the mineral type. In order to identify the influence of aluminosilicates structural differences on the modification process, adsorption experiments with organic matter and water vapor, supplemented with the DTA/TG analysis, were performed. The cation exchange capacity (CEC) value was 1454 gt 560 gt 28meqkg(-1) for zeolite (clinoptilolite), vermiculite, and mica (muscovite), respectively. Despite its CEC value, vermiculite adsorbed three times the amount of organic matter than did clinoptilolite due to the porous structure of zeolite, which acted to limit the adsorption only on the external exchangeable cations. If the loading amount is equal to the CEC or the external cation exchange capacity for clinoptilolite (ECEC approximate to 10% CEC), the monolayer will form while mineral surface will have hydrophobic character. Only one active center exists at the surface of the clinoptilolite that was identified by DTA curves with a sharp and defined peak around 300 degrees C and by the mass loss at the TG diagrams. Two significant and equal active centers were observed in vermiculite, one for the exchange of the surface cations and the other for the interlayer cations and H2O molecules. Muscovite CEC is negligible, and due to the absence of any other functional groups, the modification of this mineral was impossible.",
publisher = "Springer, Dordrecht",
journal = "Journal of Thermal Analysis and Calorimetry",
title = "Differences in coating mechanism of structurally different aluminosilicates observed through the thermal analysis",
pages = "1019-1011",
number = "2",
volume = "134",
doi = "10.1007/s10973-018-7351-3"
}
Milicević, S., Martinović, S., Milosević, V., Stojanović, J.,& Povrenović, D.. (2018). Differences in coating mechanism of structurally different aluminosilicates observed through the thermal analysis. in Journal of Thermal Analysis and Calorimetry
Springer, Dordrecht., 134(2), 1011-1019.
https://doi.org/10.1007/s10973-018-7351-3
Milicević S, Martinović S, Milosević V, Stojanović J, Povrenović D. Differences in coating mechanism of structurally different aluminosilicates observed through the thermal analysis. in Journal of Thermal Analysis and Calorimetry. 2018;134(2):1011-1019.
doi:10.1007/s10973-018-7351-3 .
Milicević, Sonja, Martinović, Sanja, Milosević, Vladan, Stojanović, Jovica, Povrenović, Dragan, "Differences in coating mechanism of structurally different aluminosilicates observed through the thermal analysis" in Journal of Thermal Analysis and Calorimetry, 134, no. 2 (2018):1011-1019,
https://doi.org/10.1007/s10973-018-7351-3 . .
3
2
2
3

Effects of structural and textural grain characteristics on leaching of sulphide minerals from a polymetallic concentrate by sodium nitrate and sulphuric acid solution

Sokić, Miroslav; Stojanović, Jovica; Marković, Branislav; Bugarčić, Mladen; Štrbac, Nada; Kamberović, Željko; Manojlović, Vaso

(Savez hemijskih inženjera, Beograd, 2017)

TY  - JOUR
AU  - Sokić, Miroslav
AU  - Stojanović, Jovica
AU  - Marković, Branislav
AU  - Bugarčić, Mladen
AU  - Štrbac, Nada
AU  - Kamberović, Željko
AU  - Manojlović, Vaso
PY  - 2017
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3654
AB  - In this paper, the influence of structural and textural characteristics of sulfide minerals on their leaching from a polymetallic concentrate by sulfuric acid and sodium nitrate solution is presented. The starting material was Pb-Zn-Cu sulphide polymetallic concentrate enriched during the flotation of a polymetallic ore in the "Rudnik" flotation plant (Rudnik - Serbia). Leaching experiments were carried out in a closed glass reactor, which provides stable hermetic conditions and allows heating at constant temperature. Chemical, XRD, qualitative and quantitative microscopic and SEM/EDX analyses were used to characterizes samples of the polymetallic concentrate and leach residue. It was determined that chalcopyrite, sphalerite, galena, pyrrhotite and quartz were present in the polymetallic concentrate. The content of sulphide minerals was 69.5%, of which 60.9% occurred as liberated grains: 88.3% of chalcopyrite, 59.3% of sphalerite, 25.1% of galena and 51.6% of pirrhotite. The rest of chalcopyrite, sphalerite, galena and pirrhotite grains were in the forms of inclusions, impregnations, and simple and complex intergrowths. During the leaching process by sodium nitrate and sulphuric acid solution, it was shown previously that the leaching rate of sulphide minerals decreased with time while a part of the sulphide minerals remained in the leach residue. After leaching at 80 degrees C for 120 min, the yields were 69.8, 82.7 and 67.1% for Cu, Zn and Fe, respectively. Lead, in the form of insoluble anglesite, remained in the leach residue. In addition to the anglesite, unleached sulfide minerals and quartz, elemental sulfur was found in the solid residue. The content of sulphide minerals was 35% of which 33.7% minerals occur independently. In specific, 54.7% of chalcopyrite, 31.9% of sphalerite, 8.2% of galena and 37.6% of pyrrhotite appear as separate grains with highly corroded surfaces. Therefore, the structural assembly of sulphide grains in the polymetallic concentrate is favourable and it is not the reason for the observed decrease in the leaching rate in the final process stages. The obtained findings may be explained by the presence of elemental sulphur that is formed during the reaction and precipitated at the grain surfaces, thus creating a diffusion barrier for the leach solution.
PB  - Savez hemijskih inženjera, Beograd
T2  - Hemijska industrija
T1  - Effects of structural and textural grain characteristics on leaching of sulphide minerals from a polymetallic concentrate by sodium nitrate and sulphuric acid solution
EP  - 469
IS  - 6
SP  - 461
VL  - 71
DO  - 10.2298/HEMIND161130006S
ER  - 
@article{
author = "Sokić, Miroslav and Stojanović, Jovica and Marković, Branislav and Bugarčić, Mladen and Štrbac, Nada and Kamberović, Željko and Manojlović, Vaso",
year = "2017",
abstract = "In this paper, the influence of structural and textural characteristics of sulfide minerals on their leaching from a polymetallic concentrate by sulfuric acid and sodium nitrate solution is presented. The starting material was Pb-Zn-Cu sulphide polymetallic concentrate enriched during the flotation of a polymetallic ore in the "Rudnik" flotation plant (Rudnik - Serbia). Leaching experiments were carried out in a closed glass reactor, which provides stable hermetic conditions and allows heating at constant temperature. Chemical, XRD, qualitative and quantitative microscopic and SEM/EDX analyses were used to characterizes samples of the polymetallic concentrate and leach residue. It was determined that chalcopyrite, sphalerite, galena, pyrrhotite and quartz were present in the polymetallic concentrate. The content of sulphide minerals was 69.5%, of which 60.9% occurred as liberated grains: 88.3% of chalcopyrite, 59.3% of sphalerite, 25.1% of galena and 51.6% of pirrhotite. The rest of chalcopyrite, sphalerite, galena and pirrhotite grains were in the forms of inclusions, impregnations, and simple and complex intergrowths. During the leaching process by sodium nitrate and sulphuric acid solution, it was shown previously that the leaching rate of sulphide minerals decreased with time while a part of the sulphide minerals remained in the leach residue. After leaching at 80 degrees C for 120 min, the yields were 69.8, 82.7 and 67.1% for Cu, Zn and Fe, respectively. Lead, in the form of insoluble anglesite, remained in the leach residue. In addition to the anglesite, unleached sulfide minerals and quartz, elemental sulfur was found in the solid residue. The content of sulphide minerals was 35% of which 33.7% minerals occur independently. In specific, 54.7% of chalcopyrite, 31.9% of sphalerite, 8.2% of galena and 37.6% of pyrrhotite appear as separate grains with highly corroded surfaces. Therefore, the structural assembly of sulphide grains in the polymetallic concentrate is favourable and it is not the reason for the observed decrease in the leaching rate in the final process stages. The obtained findings may be explained by the presence of elemental sulphur that is formed during the reaction and precipitated at the grain surfaces, thus creating a diffusion barrier for the leach solution.",
publisher = "Savez hemijskih inženjera, Beograd",
journal = "Hemijska industrija",
title = "Effects of structural and textural grain characteristics on leaching of sulphide minerals from a polymetallic concentrate by sodium nitrate and sulphuric acid solution",
pages = "469-461",
number = "6",
volume = "71",
doi = "10.2298/HEMIND161130006S"
}
Sokić, M., Stojanović, J., Marković, B., Bugarčić, M., Štrbac, N., Kamberović, Ž.,& Manojlović, V.. (2017). Effects of structural and textural grain characteristics on leaching of sulphide minerals from a polymetallic concentrate by sodium nitrate and sulphuric acid solution. in Hemijska industrija
Savez hemijskih inženjera, Beograd., 71(6), 461-469.
https://doi.org/10.2298/HEMIND161130006S
Sokić M, Stojanović J, Marković B, Bugarčić M, Štrbac N, Kamberović Ž, Manojlović V. Effects of structural and textural grain characteristics on leaching of sulphide minerals from a polymetallic concentrate by sodium nitrate and sulphuric acid solution. in Hemijska industrija. 2017;71(6):461-469.
doi:10.2298/HEMIND161130006S .
Sokić, Miroslav, Stojanović, Jovica, Marković, Branislav, Bugarčić, Mladen, Štrbac, Nada, Kamberović, Željko, Manojlović, Vaso, "Effects of structural and textural grain characteristics on leaching of sulphide minerals from a polymetallic concentrate by sodium nitrate and sulphuric acid solution" in Hemijska industrija, 71, no. 6 (2017):461-469,
https://doi.org/10.2298/HEMIND161130006S . .
3
1
2

In vitro investigation of electrophoretically deposited bioactive hydroxyapatite/chitosan coatings reinforced by graphene

Đošić, Marija; Eraković, Sanja; Janković, Ana; Vukašinović-Sekulić, Maja; Matić, Ivana Z.; Stojanović, Jovica; Rhee, Kyong Yop; Mišković-Stanković, Vesna; Park, Soo-Jin

(Elsevier Science Inc, New York, 2017)

TY  - JOUR
AU  - Đošić, Marija
AU  - Eraković, Sanja
AU  - Janković, Ana
AU  - Vukašinović-Sekulić, Maja
AU  - Matić, Ivana Z.
AU  - Stojanović, Jovica
AU  - Rhee, Kyong Yop
AU  - Mišković-Stanković, Vesna
AU  - Park, Soo-Jin
PY  - 2017
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3703
AB  - Graphene (Gr) and natural polymer chitosan (CS) were introduced to hydroxyapatite (HAP) to produce a three-component composite coating, which was fabricated by cathodic electrophoretic deposition on Ti substrates in an ethanol suspension. These HAP/CS/Gr coatings were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS) and electrochemical measurements and found that the graphene into HAP/CS composites significantly improves their morphology, thermal stability, and bioactivity. Both HAP/CS and HAP/CS/Gr composite coatings are classified as non-cytotoxic when tested against healthy peripheral blood mononuclear cells (PBMC), while antibacterial activity against Staphylococcus aureus and Escherichia coil could not be verified.
PB  - Elsevier Science Inc, New York
T2  - Journal of Industrial and Engineering Chemistry
T1  - In vitro investigation of electrophoretically deposited bioactive hydroxyapatite/chitosan coatings reinforced by graphene
EP  - 347
SP  - 336
VL  - 47
DO  - 10.1016/j.jiec.2016.12.004
ER  - 
@article{
author = "Đošić, Marija and Eraković, Sanja and Janković, Ana and Vukašinović-Sekulić, Maja and Matić, Ivana Z. and Stojanović, Jovica and Rhee, Kyong Yop and Mišković-Stanković, Vesna and Park, Soo-Jin",
year = "2017",
abstract = "Graphene (Gr) and natural polymer chitosan (CS) were introduced to hydroxyapatite (HAP) to produce a three-component composite coating, which was fabricated by cathodic electrophoretic deposition on Ti substrates in an ethanol suspension. These HAP/CS/Gr coatings were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS) and electrochemical measurements and found that the graphene into HAP/CS composites significantly improves their morphology, thermal stability, and bioactivity. Both HAP/CS and HAP/CS/Gr composite coatings are classified as non-cytotoxic when tested against healthy peripheral blood mononuclear cells (PBMC), while antibacterial activity against Staphylococcus aureus and Escherichia coil could not be verified.",
publisher = "Elsevier Science Inc, New York",
journal = "Journal of Industrial and Engineering Chemistry",
title = "In vitro investigation of electrophoretically deposited bioactive hydroxyapatite/chitosan coatings reinforced by graphene",
pages = "347-336",
volume = "47",
doi = "10.1016/j.jiec.2016.12.004"
}
Đošić, M., Eraković, S., Janković, A., Vukašinović-Sekulić, M., Matić, I. Z., Stojanović, J., Rhee, K. Y., Mišković-Stanković, V.,& Park, S.. (2017). In vitro investigation of electrophoretically deposited bioactive hydroxyapatite/chitosan coatings reinforced by graphene. in Journal of Industrial and Engineering Chemistry
Elsevier Science Inc, New York., 47, 336-347.
https://doi.org/10.1016/j.jiec.2016.12.004
Đošić M, Eraković S, Janković A, Vukašinović-Sekulić M, Matić IZ, Stojanović J, Rhee KY, Mišković-Stanković V, Park S. In vitro investigation of electrophoretically deposited bioactive hydroxyapatite/chitosan coatings reinforced by graphene. in Journal of Industrial and Engineering Chemistry. 2017;47:336-347.
doi:10.1016/j.jiec.2016.12.004 .
Đošić, Marija, Eraković, Sanja, Janković, Ana, Vukašinović-Sekulić, Maja, Matić, Ivana Z., Stojanović, Jovica, Rhee, Kyong Yop, Mišković-Stanković, Vesna, Park, Soo-Jin, "In vitro investigation of electrophoretically deposited bioactive hydroxyapatite/chitosan coatings reinforced by graphene" in Journal of Industrial and Engineering Chemistry, 47 (2017):336-347,
https://doi.org/10.1016/j.jiec.2016.12.004 . .
47
35
45

Bioactive glass-ceramics prepared by powder sintering and crystallization of polyphosphate glass containing strontium

Topalović, Vladimir S.; Grujić, Snežana; Živanović, Vladimir D.; Matijašević, Srđan D.; Nikolić, Jelena D.; Stojanović, Jovica; Smiljanić, Sonja

(Elsevier Sci Ltd, Oxford, 2017)

TY  - JOUR
AU  - Topalović, Vladimir S.
AU  - Grujić, Snežana
AU  - Živanović, Vladimir D.
AU  - Matijašević, Srđan D.
AU  - Nikolić, Jelena D.
AU  - Stojanović, Jovica
AU  - Smiljanić, Sonja
PY  - 2017
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3583
AB  - Melt-quenching method was employed for obtaining a glass-ceramic with the following composition 42P(2)O(5). 40CaO.5SrO.10Na(2)O.3TiO(2) (mol%) glass. The crystallization and sintering behavior of glass have been studied by using DTA, HSM, XRD, FTIR and SEM methods. It was determined that the surface and volume crystallization mechanisms act simultaneously in bulk glass samples. The comparison of DTA and HSM data revealed that the sintering and crystallization processes are independent. The sintered calcium phosphate glass ceramic which contained bioactive beta-Ca-3(PO4)(2) and beta-Ca2P2O7 phases was successfully prepared. It was determined that during crystallization the primary phase in the precipitate was beta-Ca(PO3)(2). Other phases appearing in the resulting glass-ceramic were: alpha-Ca2P2O7, gamma-Ca2PO7, Ca4P6O19 and CaHPO4(H2O)(2). Crystalline phases containing Sr and Ti were not detected. SEM analysis of the glass-ceramic microstructure revealed surface crystallization of glass particles and plate-like morphology of crystal growth. The result of the in vitro bioactivity showed that no apatite layer was formed on the surface of the as-prepared glass-ceramic samples after immersion in the simulated body fluid (SBF).
PB  - Elsevier Sci Ltd, Oxford
T2  - Ceramics International
T1  - Bioactive glass-ceramics prepared by powder sintering and crystallization of polyphosphate glass containing strontium
EP  - 12069
IS  - 15
SP  - 12061
VL  - 43
DO  - 10.1016/j.ceramint.2017.06.061
ER  - 
@article{
author = "Topalović, Vladimir S. and Grujić, Snežana and Živanović, Vladimir D. and Matijašević, Srđan D. and Nikolić, Jelena D. and Stojanović, Jovica and Smiljanić, Sonja",
year = "2017",
abstract = "Melt-quenching method was employed for obtaining a glass-ceramic with the following composition 42P(2)O(5). 40CaO.5SrO.10Na(2)O.3TiO(2) (mol%) glass. The crystallization and sintering behavior of glass have been studied by using DTA, HSM, XRD, FTIR and SEM methods. It was determined that the surface and volume crystallization mechanisms act simultaneously in bulk glass samples. The comparison of DTA and HSM data revealed that the sintering and crystallization processes are independent. The sintered calcium phosphate glass ceramic which contained bioactive beta-Ca-3(PO4)(2) and beta-Ca2P2O7 phases was successfully prepared. It was determined that during crystallization the primary phase in the precipitate was beta-Ca(PO3)(2). Other phases appearing in the resulting glass-ceramic were: alpha-Ca2P2O7, gamma-Ca2PO7, Ca4P6O19 and CaHPO4(H2O)(2). Crystalline phases containing Sr and Ti were not detected. SEM analysis of the glass-ceramic microstructure revealed surface crystallization of glass particles and plate-like morphology of crystal growth. The result of the in vitro bioactivity showed that no apatite layer was formed on the surface of the as-prepared glass-ceramic samples after immersion in the simulated body fluid (SBF).",
publisher = "Elsevier Sci Ltd, Oxford",
journal = "Ceramics International",
title = "Bioactive glass-ceramics prepared by powder sintering and crystallization of polyphosphate glass containing strontium",
pages = "12069-12061",
number = "15",
volume = "43",
doi = "10.1016/j.ceramint.2017.06.061"
}
Topalović, V. S., Grujić, S., Živanović, V. D., Matijašević, S. D., Nikolić, J. D., Stojanović, J.,& Smiljanić, S.. (2017). Bioactive glass-ceramics prepared by powder sintering and crystallization of polyphosphate glass containing strontium. in Ceramics International
Elsevier Sci Ltd, Oxford., 43(15), 12061-12069.
https://doi.org/10.1016/j.ceramint.2017.06.061
Topalović VS, Grujić S, Živanović VD, Matijašević SD, Nikolić JD, Stojanović J, Smiljanić S. Bioactive glass-ceramics prepared by powder sintering and crystallization of polyphosphate glass containing strontium. in Ceramics International. 2017;43(15):12061-12069.
doi:10.1016/j.ceramint.2017.06.061 .
Topalović, Vladimir S., Grujić, Snežana, Živanović, Vladimir D., Matijašević, Srđan D., Nikolić, Jelena D., Stojanović, Jovica, Smiljanić, Sonja, "Bioactive glass-ceramics prepared by powder sintering and crystallization of polyphosphate glass containing strontium" in Ceramics International, 43, no. 15 (2017):12061-12069,
https://doi.org/10.1016/j.ceramint.2017.06.061 . .
13
9
14

Kinetics of barite reduction from refractory barite-sulphide ore

Sokić, Miroslav; Matković, Vladislav; Stojanović, Jovica; Marković, Branislav; Manojlović, Vaso

(Savez inženjera metalurgije Srbije, Beograd, 2016)

TY  - JOUR
AU  - Sokić, Miroslav
AU  - Matković, Vladislav
AU  - Stojanović, Jovica
AU  - Marković, Branislav
AU  - Manojlović, Vaso
PY  - 2016
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3310
AB  - Refractory sulphide-barite ore was reduced with carbon in order to release lead, zinc, and copper sulphide from barite-pyrite base. Mineralogical investigations showed that due to the complex structural-textural relationships of lead, copper and zinc minerals with gangue minerals, it is not possible to enrich the ore using the conventional methods of mineral processing. The influence of temperature and time was studied to optimize the conditions, and to determine the kinetics of the barite reduction. The maximum removal of barite from ore was 96.7% at 900oC after 180 min. Chemically controlled kinetic model showed the best compliance with the experimental data. An activation energy of 142 kJ/mol was found.
PB  - Savez inženjera metalurgije Srbije, Beograd
T2  - Metallurgical & Materials Engineering
T1  - Kinetics of barite reduction from refractory barite-sulphide ore
EP  - 268
IS  - 4
SP  - 261
VL  - 22
DO  - 10.30544/237
ER  - 
@article{
author = "Sokić, Miroslav and Matković, Vladislav and Stojanović, Jovica and Marković, Branislav and Manojlović, Vaso",
year = "2016",
abstract = "Refractory sulphide-barite ore was reduced with carbon in order to release lead, zinc, and copper sulphide from barite-pyrite base. Mineralogical investigations showed that due to the complex structural-textural relationships of lead, copper and zinc minerals with gangue minerals, it is not possible to enrich the ore using the conventional methods of mineral processing. The influence of temperature and time was studied to optimize the conditions, and to determine the kinetics of the barite reduction. The maximum removal of barite from ore was 96.7% at 900oC after 180 min. Chemically controlled kinetic model showed the best compliance with the experimental data. An activation energy of 142 kJ/mol was found.",
publisher = "Savez inženjera metalurgije Srbije, Beograd",
journal = "Metallurgical & Materials Engineering",
title = "Kinetics of barite reduction from refractory barite-sulphide ore",
pages = "268-261",
number = "4",
volume = "22",
doi = "10.30544/237"
}
Sokić, M., Matković, V., Stojanović, J., Marković, B.,& Manojlović, V.. (2016). Kinetics of barite reduction from refractory barite-sulphide ore. in Metallurgical & Materials Engineering
Savez inženjera metalurgije Srbije, Beograd., 22(4), 261-268.
https://doi.org/10.30544/237
Sokić M, Matković V, Stojanović J, Marković B, Manojlović V. Kinetics of barite reduction from refractory barite-sulphide ore. in Metallurgical & Materials Engineering. 2016;22(4):261-268.
doi:10.30544/237 .
Sokić, Miroslav, Matković, Vladislav, Stojanović, Jovica, Marković, Branislav, Manojlović, Vaso, "Kinetics of barite reduction from refractory barite-sulphide ore" in Metallurgical & Materials Engineering, 22, no. 4 (2016):261-268,
https://doi.org/10.30544/237 . .
1
1

Crystallization and sintering behaviors of the polyphosphate glass doped with Zn and Mn

Nikolić, Jelena D.; Živanović, Vladimir D.; Matijašević, Srđan D.; Stojanović, Jovica; Grujić, Snežana; Smiljanić, Sonja; Topalović, Vladimir S.

(Springer, Dordrecht, 2016)

TY  - JOUR
AU  - Nikolić, Jelena D.
AU  - Živanović, Vladimir D.
AU  - Matijašević, Srđan D.
AU  - Stojanović, Jovica
AU  - Grujić, Snežana
AU  - Smiljanić, Sonja
AU  - Topalović, Vladimir S.
PY  - 2016
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3398
AB  - The crystallization and sintering behaviors of polyphosphate glass doped with trace elements Zn and Mn were examined. The heating experiments on bulk and powder glass samples were performed. The parent glass revealed low crystallization ability and the glass crystallization carried out under simultaneous acting of the surface and volume mechanisms. The bulk glass sample isothermally heated at T
PB  - Springer, Dordrecht
T2  - Journal of Thermal Analysis and Calorimetry
T1  - Crystallization and sintering behaviors of the polyphosphate glass doped with Zn and Mn
EP  - 592
IS  - 2
SP  - 585
VL  - 124
DO  - 10.1007/s10973-015-5184-x
ER  - 
@article{
author = "Nikolić, Jelena D. and Živanović, Vladimir D. and Matijašević, Srđan D. and Stojanović, Jovica and Grujić, Snežana and Smiljanić, Sonja and Topalović, Vladimir S.",
year = "2016",
abstract = "The crystallization and sintering behaviors of polyphosphate glass doped with trace elements Zn and Mn were examined. The heating experiments on bulk and powder glass samples were performed. The parent glass revealed low crystallization ability and the glass crystallization carried out under simultaneous acting of the surface and volume mechanisms. The bulk glass sample isothermally heated at T",
publisher = "Springer, Dordrecht",
journal = "Journal of Thermal Analysis and Calorimetry",
title = "Crystallization and sintering behaviors of the polyphosphate glass doped with Zn and Mn",
pages = "592-585",
number = "2",
volume = "124",
doi = "10.1007/s10973-015-5184-x"
}
Nikolić, J. D., Živanović, V. D., Matijašević, S. D., Stojanović, J., Grujić, S., Smiljanić, S.,& Topalović, V. S.. (2016). Crystallization and sintering behaviors of the polyphosphate glass doped with Zn and Mn. in Journal of Thermal Analysis and Calorimetry
Springer, Dordrecht., 124(2), 585-592.
https://doi.org/10.1007/s10973-015-5184-x
Nikolić JD, Živanović VD, Matijašević SD, Stojanović J, Grujić S, Smiljanić S, Topalović VS. Crystallization and sintering behaviors of the polyphosphate glass doped with Zn and Mn. in Journal of Thermal Analysis and Calorimetry. 2016;124(2):585-592.
doi:10.1007/s10973-015-5184-x .
Nikolić, Jelena D., Živanović, Vladimir D., Matijašević, Srđan D., Stojanović, Jovica, Grujić, Snežana, Smiljanić, Sonja, Topalović, Vladimir S., "Crystallization and sintering behaviors of the polyphosphate glass doped with Zn and Mn" in Journal of Thermal Analysis and Calorimetry, 124, no. 2 (2016):585-592,
https://doi.org/10.1007/s10973-015-5184-x . .
5
5
5

DTA study of the crystallization of Li2O-Nb2O5-SiO2-TiO2 glass

Živanović, Vladimir D.; Tošić, Mihajlo B.; Grujić, Snežana; Matijašević, Srđan D.; Stojanović, Jovica; Nikolić, J. D.; Smiljanić, Sonja

(Springer, Dordrecht, 2015)

TY  - JOUR
AU  - Živanović, Vladimir D.
AU  - Tošić, Mihajlo B.
AU  - Grujić, Snežana
AU  - Matijašević, Srđan D.
AU  - Stojanović, Jovica
AU  - Nikolić, J. D.
AU  - Smiljanić, Sonja
PY  - 2015
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3034
AB  - In this study, the crystallization of 30Li(2)O center dot 15Nb(2)O(5)center dot 50SiO(2)center dot 5TiO(2) (mol%) glass was examined. The parent glass was prepared by the standard melt quenching method, and the investigations were performed under non-isothermal and isothermal conditions using the DTA, XRD, SEM and EDS methods. The results revealed primary crystallization of this glass and the dendritic morphology of crystal growth. Three crystalline phases were formed in the glass matrix during crystallization, whereby LiNbO3 was formed as the primary phase, followed by Li2Si2O5 and SiO2 as the secondary. The surface and volume mechanisms of crystallization occur. The condition that both the mechanisms were dominant was determined. In the case of volume crystallization, the characteristics of the nucleation process were examined. The kinetic parameters of crystallization under different mechanisms of crystallization were determined.
PB  - Springer, Dordrecht
T2  - Journal of Thermal Analysis and Calorimetry
T1  - DTA study of the crystallization of Li2O-Nb2O5-SiO2-TiO2 glass
EP  - 1661
IS  - 3
SP  - 1653
VL  - 119
DO  - 10.1007/s10973-015-4390-x
ER  - 
@article{
author = "Živanović, Vladimir D. and Tošić, Mihajlo B. and Grujić, Snežana and Matijašević, Srđan D. and Stojanović, Jovica and Nikolić, J. D. and Smiljanić, Sonja",
year = "2015",
abstract = "In this study, the crystallization of 30Li(2)O center dot 15Nb(2)O(5)center dot 50SiO(2)center dot 5TiO(2) (mol%) glass was examined. The parent glass was prepared by the standard melt quenching method, and the investigations were performed under non-isothermal and isothermal conditions using the DTA, XRD, SEM and EDS methods. The results revealed primary crystallization of this glass and the dendritic morphology of crystal growth. Three crystalline phases were formed in the glass matrix during crystallization, whereby LiNbO3 was formed as the primary phase, followed by Li2Si2O5 and SiO2 as the secondary. The surface and volume mechanisms of crystallization occur. The condition that both the mechanisms were dominant was determined. In the case of volume crystallization, the characteristics of the nucleation process were examined. The kinetic parameters of crystallization under different mechanisms of crystallization were determined.",
publisher = "Springer, Dordrecht",
journal = "Journal of Thermal Analysis and Calorimetry",
title = "DTA study of the crystallization of Li2O-Nb2O5-SiO2-TiO2 glass",
pages = "1661-1653",
number = "3",
volume = "119",
doi = "10.1007/s10973-015-4390-x"
}
Živanović, V. D., Tošić, M. B., Grujić, S., Matijašević, S. D., Stojanović, J., Nikolić, J. D.,& Smiljanić, S.. (2015). DTA study of the crystallization of Li2O-Nb2O5-SiO2-TiO2 glass. in Journal of Thermal Analysis and Calorimetry
Springer, Dordrecht., 119(3), 1653-1661.
https://doi.org/10.1007/s10973-015-4390-x
Živanović VD, Tošić MB, Grujić S, Matijašević SD, Stojanović J, Nikolić JD, Smiljanić S. DTA study of the crystallization of Li2O-Nb2O5-SiO2-TiO2 glass. in Journal of Thermal Analysis and Calorimetry. 2015;119(3):1653-1661.
doi:10.1007/s10973-015-4390-x .
Živanović, Vladimir D., Tošić, Mihajlo B., Grujić, Snežana, Matijašević, Srđan D., Stojanović, Jovica, Nikolić, J. D., Smiljanić, Sonja, "DTA study of the crystallization of Li2O-Nb2O5-SiO2-TiO2 glass" in Journal of Thermal Analysis and Calorimetry, 119, no. 3 (2015):1653-1661,
https://doi.org/10.1007/s10973-015-4390-x . .
4
4
4

Crystallization and sinterability of glass-ceramics in the system La2O3-SrO-B2O3

Smiljanić, Sonja; Grujić, Snežana; Tošić, Mihajlo B.; Živanović, Vladimir D.; Stojanović, Jovica; Matijašević, Srđan D.; Nikolić, Jelena D.

(Elsevier Sci Ltd, Oxford, 2014)

TY  - JOUR
AU  - Smiljanić, Sonja
AU  - Grujić, Snežana
AU  - Tošić, Mihajlo B.
AU  - Živanović, Vladimir D.
AU  - Stojanović, Jovica
AU  - Matijašević, Srđan D.
AU  - Nikolić, Jelena D.
PY  - 2014
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/2800
AB  - Glasses with a constant B2O3 and an increasing La2O3 content in the system La2O3-SrO-B2O3 were obtained by the usual melt quenching procedure. The crystallization and sinterability of the glasses were investigated by hot stage microscopy (HSM), differential thermal analysis (DTA), X-ray diffraction (XRD) analysis, transmission electron microscopy (TEM) and scanning electron microscopy (SEM). XRD analysis of the bulk samples evidenced the formation of the crystalline phases: La2SrB10O19, SrB6O10 and SrLaBO4. XRD and TEM/SAED analyses showed a polymorphic crystallization of the glass sample containing 14.3 mol% La2O3 with precipitation of the La2SrB10O19 phase. SEM analysis confirmed the surface crystallization mechanism of this sample. The kinetics of crystallization of the same sample was examined by DTA and the activation energy of crystal growth was calculated by the Kissinger model to be E-a=458 +/- 63 kJ mol(-1).
PB  - Elsevier Sci Ltd, Oxford
T2  - Ceramics International
T1  - Crystallization and sinterability of glass-ceramics in the system La2O3-SrO-B2O3
EP  - 305
IS  - 1
SP  - 297
VL  - 40
DO  - 10.1016/j.ceramint.2013.06.002
ER  - 
@article{
author = "Smiljanić, Sonja and Grujić, Snežana and Tošić, Mihajlo B. and Živanović, Vladimir D. and Stojanović, Jovica and Matijašević, Srđan D. and Nikolić, Jelena D.",
year = "2014",
abstract = "Glasses with a constant B2O3 and an increasing La2O3 content in the system La2O3-SrO-B2O3 were obtained by the usual melt quenching procedure. The crystallization and sinterability of the glasses were investigated by hot stage microscopy (HSM), differential thermal analysis (DTA), X-ray diffraction (XRD) analysis, transmission electron microscopy (TEM) and scanning electron microscopy (SEM). XRD analysis of the bulk samples evidenced the formation of the crystalline phases: La2SrB10O19, SrB6O10 and SrLaBO4. XRD and TEM/SAED analyses showed a polymorphic crystallization of the glass sample containing 14.3 mol% La2O3 with precipitation of the La2SrB10O19 phase. SEM analysis confirmed the surface crystallization mechanism of this sample. The kinetics of crystallization of the same sample was examined by DTA and the activation energy of crystal growth was calculated by the Kissinger model to be E-a=458 +/- 63 kJ mol(-1).",
publisher = "Elsevier Sci Ltd, Oxford",
journal = "Ceramics International",
title = "Crystallization and sinterability of glass-ceramics in the system La2O3-SrO-B2O3",
pages = "305-297",
number = "1",
volume = "40",
doi = "10.1016/j.ceramint.2013.06.002"
}
Smiljanić, S., Grujić, S., Tošić, M. B., Živanović, V. D., Stojanović, J., Matijašević, S. D.,& Nikolić, J. D.. (2014). Crystallization and sinterability of glass-ceramics in the system La2O3-SrO-B2O3. in Ceramics International
Elsevier Sci Ltd, Oxford., 40(1), 297-305.
https://doi.org/10.1016/j.ceramint.2013.06.002
Smiljanić S, Grujić S, Tošić MB, Živanović VD, Stojanović J, Matijašević SD, Nikolić JD. Crystallization and sinterability of glass-ceramics in the system La2O3-SrO-B2O3. in Ceramics International. 2014;40(1):297-305.
doi:10.1016/j.ceramint.2013.06.002 .
Smiljanić, Sonja, Grujić, Snežana, Tošić, Mihajlo B., Živanović, Vladimir D., Stojanović, Jovica, Matijašević, Srđan D., Nikolić, Jelena D., "Crystallization and sinterability of glass-ceramics in the system La2O3-SrO-B2O3" in Ceramics International, 40, no. 1 (2014):297-305,
https://doi.org/10.1016/j.ceramint.2013.06.002 . .
16
14
19

Preparation of glass-ceramic in Li2O-Al2O3-GeO2-P2O5 system

Nikolić, Jelena D.; Smiljanić, Sonja; Matijašević, Srđan D.; Živanović, Vladimir D.; Tošić, Mihajlo B.; Grujić, Snežana; Stojanović, Jovica

(University of Novi Sad, 2013)

TY  - JOUR
AU  - Nikolić, Jelena D.
AU  - Smiljanić, Sonja
AU  - Matijašević, Srđan D.
AU  - Živanović, Vladimir D.
AU  - Tošić, Mihajlo B.
AU  - Grujić, Snežana
AU  - Stojanović, Jovica
PY  - 2013
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/2333
AB  - The results of preparation and structural characterization of glass-ceramics from the system Li2O-Al2O3-GeO2-P2O5 are shown in this paper. The crystallization behaviour of the selected glass was examined under non-isothermal and isothermal crystallization conditions. DTA, XRD and SEM methods were employed for analyses. It was confirmed that this glass crystallizes by the volume crystallization mechanism. The results also showed that the glass crystallize by primary crystallization. As a primary phase the LiGe2(PO4)3 is formed and the traces of GeO2 as a secondary one is present. The crystallization process occurred at a high homogeneous nucleation rate and the spherical morphology of crystal growth. By applying the Kissinger relation the activation energy of crystal growth Ea = 462 kJ/mol was determined.
PB  - University of Novi Sad
T2  - Processing and Application of Ceramics
T1  - Preparation of glass-ceramic in Li2O-Al2O3-GeO2-P2O5 system
EP  - 151
IS  - 4
SP  - 147
VL  - 7
UR  - https://hdl.handle.net/21.15107/rcub_technorep_2333
ER  - 
@article{
author = "Nikolić, Jelena D. and Smiljanić, Sonja and Matijašević, Srđan D. and Živanović, Vladimir D. and Tošić, Mihajlo B. and Grujić, Snežana and Stojanović, Jovica",
year = "2013",
abstract = "The results of preparation and structural characterization of glass-ceramics from the system Li2O-Al2O3-GeO2-P2O5 are shown in this paper. The crystallization behaviour of the selected glass was examined under non-isothermal and isothermal crystallization conditions. DTA, XRD and SEM methods were employed for analyses. It was confirmed that this glass crystallizes by the volume crystallization mechanism. The results also showed that the glass crystallize by primary crystallization. As a primary phase the LiGe2(PO4)3 is formed and the traces of GeO2 as a secondary one is present. The crystallization process occurred at a high homogeneous nucleation rate and the spherical morphology of crystal growth. By applying the Kissinger relation the activation energy of crystal growth Ea = 462 kJ/mol was determined.",
publisher = "University of Novi Sad",
journal = "Processing and Application of Ceramics",
title = "Preparation of glass-ceramic in Li2O-Al2O3-GeO2-P2O5 system",
pages = "151-147",
number = "4",
volume = "7",
url = "https://hdl.handle.net/21.15107/rcub_technorep_2333"
}
Nikolić, J. D., Smiljanić, S., Matijašević, S. D., Živanović, V. D., Tošić, M. B., Grujić, S.,& Stojanović, J.. (2013). Preparation of glass-ceramic in Li2O-Al2O3-GeO2-P2O5 system. in Processing and Application of Ceramics
University of Novi Sad., 7(4), 147-151.
https://hdl.handle.net/21.15107/rcub_technorep_2333
Nikolić JD, Smiljanić S, Matijašević SD, Živanović VD, Tošić MB, Grujić S, Stojanović J. Preparation of glass-ceramic in Li2O-Al2O3-GeO2-P2O5 system. in Processing and Application of Ceramics. 2013;7(4):147-151.
https://hdl.handle.net/21.15107/rcub_technorep_2333 .
Nikolić, Jelena D., Smiljanić, Sonja, Matijašević, Srđan D., Živanović, Vladimir D., Tošić, Mihajlo B., Grujić, Snežana, Stojanović, Jovica, "Preparation of glass-ceramic in Li2O-Al2O3-GeO2-P2O5 system" in Processing and Application of Ceramics, 7, no. 4 (2013):147-151,
https://hdl.handle.net/21.15107/rcub_technorep_2333 .
8

Removal of heavy metals from aqueous solution using natural and fe(iii) oxyhydroxide clinoptilolite

Milicević, Sonja; Milosević, Vladan; Povrenović, Dragan; Stojanović, Jovica; Martinović, Sanja; Babić, Biljana M.

(Clay Minerals Soc, Chantilly, 2013)

TY  - JOUR
AU  - Milicević, Sonja
AU  - Milosević, Vladan
AU  - Povrenović, Dragan
AU  - Stojanović, Jovica
AU  - Martinović, Sanja
AU  - Babić, Biljana M.
PY  - 2013
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/2398
AB  - The increasing levels of industrial wastewater released to the environment present a serious threat to human health, living resources, and ecological systems. Fe-modified zeolites were developed and tested for removal of Cu2+ and Zn2+ from contaminated water. The surfaces of the naturally occurring zeolite, clinoptilolite, were modified with Fe(III) oxyhydroxides using three different methods, denoted I, II, and III (FeCli(1), FeCli(2), and FeNaCli(1), respectively). The oxyhydroxides were prepared in Method I using 0.1 M FeCl3 center dot 6H(2)O in an acetate buffer (pH = 3.6); in Method II, using 10% FeCl3 center dot 6H(2)O solution in 0.1 M KOH (pH = 10); and Method III was the same as Method I except the clinoptilolite was pretreated with NaCl. Newly synthesized materials from these three methods were then tested for their ability to enhance the sorption capacity for Cu and Zn compared to the natural sample (Cli). Powder X-ray diffraction measurements and the chemical composition of these modified samples confirmed that clinoptilolite maintained its structure while amorphous Fe3+ species were synthesized. The specific surface area (BET method) of both the natural and modified clinoptilolite increased by 2 and 7.5 times for Methods I and II, respectively. Scanning electron microscopy and energy dispersive X-ray spectroscopy revealed that CaO was formed during Method I (FeCli(1)). Throughout the adsorption process, the hydrolysis of CaO and the release of OH- caused the precipitation of Cu and Zn hydroxide, which made the determination of the sorption capacity of FeCli(1) impossible. This phenomenon was avoided in Method III (FeNaCli(1)) because of the absence of exchangeable Ca2+. The adsorption experiments with Method II resulted in double-enchanced adsoprtion capacity. Laboratory batch experiments revealed that the sorption capacities increased in the following order: Cli  lt  FeCli(2)  lt  FeNaCli(1), for Cu: 0.121 mmol/g  lt  0.251 mmol/g  lt  0.403 mmol/g and for Zn: 0.128 mmol/g  lt  0.234 mmol/g  lt  0.381 mmol/g.
PB  - Clay Minerals Soc, Chantilly
T2  - Clays and Clay Minerals
T1  - Removal of heavy metals from aqueous solution using natural and fe(iii) oxyhydroxide clinoptilolite
EP  - 516
IS  - 6
SP  - 508
VL  - 61
DO  - 10.1346/CCMN.2013.0610603
ER  - 
@article{
author = "Milicević, Sonja and Milosević, Vladan and Povrenović, Dragan and Stojanović, Jovica and Martinović, Sanja and Babić, Biljana M.",
year = "2013",
abstract = "The increasing levels of industrial wastewater released to the environment present a serious threat to human health, living resources, and ecological systems. Fe-modified zeolites were developed and tested for removal of Cu2+ and Zn2+ from contaminated water. The surfaces of the naturally occurring zeolite, clinoptilolite, were modified with Fe(III) oxyhydroxides using three different methods, denoted I, II, and III (FeCli(1), FeCli(2), and FeNaCli(1), respectively). The oxyhydroxides were prepared in Method I using 0.1 M FeCl3 center dot 6H(2)O in an acetate buffer (pH = 3.6); in Method II, using 10% FeCl3 center dot 6H(2)O solution in 0.1 M KOH (pH = 10); and Method III was the same as Method I except the clinoptilolite was pretreated with NaCl. Newly synthesized materials from these three methods were then tested for their ability to enhance the sorption capacity for Cu and Zn compared to the natural sample (Cli). Powder X-ray diffraction measurements and the chemical composition of these modified samples confirmed that clinoptilolite maintained its structure while amorphous Fe3+ species were synthesized. The specific surface area (BET method) of both the natural and modified clinoptilolite increased by 2 and 7.5 times for Methods I and II, respectively. Scanning electron microscopy and energy dispersive X-ray spectroscopy revealed that CaO was formed during Method I (FeCli(1)). Throughout the adsorption process, the hydrolysis of CaO and the release of OH- caused the precipitation of Cu and Zn hydroxide, which made the determination of the sorption capacity of FeCli(1) impossible. This phenomenon was avoided in Method III (FeNaCli(1)) because of the absence of exchangeable Ca2+. The adsorption experiments with Method II resulted in double-enchanced adsoprtion capacity. Laboratory batch experiments revealed that the sorption capacities increased in the following order: Cli  lt  FeCli(2)  lt  FeNaCli(1), for Cu: 0.121 mmol/g  lt  0.251 mmol/g  lt  0.403 mmol/g and for Zn: 0.128 mmol/g  lt  0.234 mmol/g  lt  0.381 mmol/g.",
publisher = "Clay Minerals Soc, Chantilly",
journal = "Clays and Clay Minerals",
title = "Removal of heavy metals from aqueous solution using natural and fe(iii) oxyhydroxide clinoptilolite",
pages = "516-508",
number = "6",
volume = "61",
doi = "10.1346/CCMN.2013.0610603"
}
Milicević, S., Milosević, V., Povrenović, D., Stojanović, J., Martinović, S.,& Babić, B. M.. (2013). Removal of heavy metals from aqueous solution using natural and fe(iii) oxyhydroxide clinoptilolite. in Clays and Clay Minerals
Clay Minerals Soc, Chantilly., 61(6), 508-516.
https://doi.org/10.1346/CCMN.2013.0610603
Milicević S, Milosević V, Povrenović D, Stojanović J, Martinović S, Babić BM. Removal of heavy metals from aqueous solution using natural and fe(iii) oxyhydroxide clinoptilolite. in Clays and Clay Minerals. 2013;61(6):508-516.
doi:10.1346/CCMN.2013.0610603 .
Milicević, Sonja, Milosević, Vladan, Povrenović, Dragan, Stojanović, Jovica, Martinović, Sanja, Babić, Biljana M., "Removal of heavy metals from aqueous solution using natural and fe(iii) oxyhydroxide clinoptilolite" in Clays and Clay Minerals, 61, no. 6 (2013):508-516,
https://doi.org/10.1346/CCMN.2013.0610603 . .
12
8

The crystallization of potassium germanate glass with high content of niobium oxide

Matijašević, Srđan D.; Tošić, Mihajlo B.; Stojanović, Jovica; Grujić, Snežana; Živanović, Vladimir D.; Nikolić, Jelena D.; Đošić, Marija

(University of Chemistry and Technology, Prague, 2012)

TY  - JOUR
AU  - Matijašević, Srđan D.
AU  - Tošić, Mihajlo B.
AU  - Stojanović, Jovica
AU  - Grujić, Snežana
AU  - Živanović, Vladimir D.
AU  - Nikolić, Jelena D.
AU  - Đošić, Marija
PY  - 2012
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1981
AB  - Potassium germanate glass with molar ratio [GeO2]/[K2O] = 1.2 and Nb2O5 content of 34 mol% have been synthesized by a melt-quenching method. The crystallization behavior under non-isothermal and isothermal crystallization conditions was investigated. The results showed that this glass exposed complex primary crystallization. In the temperature range  lt  800 degrees C primary phase is K3.8Nb5Ge3O20.4, while K6Nb6Ge4O26 appeared as primary phase at temperatures  gt  800 degrees C. K10Nb22Ge4O68 and metastable KNbO3 and K4Nb6O17 were formed as secondary phases. The crystallization commenced at T  gt  640 degrees C with high homogeneous nucleation rate and spherulite crystal growth morphology. DTA curves recorded for powder samples particle size  lt  0.1 mm revealed three exothermic peaks and three endothermic peaks within temperature range of T = 640-940 degrees C, while the DTA curves recorded for powder samples particle size  gt  0.1 mm showed two exothermic peaks and two endothermic peaks within temperature range of T = 640-1020 degrees C. The analysis of the dominant crystallization mechanism of powder glass sample and kinetics of crystallization is presented.
PB  - University of Chemistry and Technology, Prague
T2  - Ceramics - Silikaty
T1  - The crystallization of potassium germanate glass with high content of niobium oxide
EP  - 68
IS  - 1
SP  - 61
VL  - 56
UR  - https://hdl.handle.net/21.15107/rcub_technorep_1981
ER  - 
@article{
author = "Matijašević, Srđan D. and Tošić, Mihajlo B. and Stojanović, Jovica and Grujić, Snežana and Živanović, Vladimir D. and Nikolić, Jelena D. and Đošić, Marija",
year = "2012",
abstract = "Potassium germanate glass with molar ratio [GeO2]/[K2O] = 1.2 and Nb2O5 content of 34 mol% have been synthesized by a melt-quenching method. The crystallization behavior under non-isothermal and isothermal crystallization conditions was investigated. The results showed that this glass exposed complex primary crystallization. In the temperature range  lt  800 degrees C primary phase is K3.8Nb5Ge3O20.4, while K6Nb6Ge4O26 appeared as primary phase at temperatures  gt  800 degrees C. K10Nb22Ge4O68 and metastable KNbO3 and K4Nb6O17 were formed as secondary phases. The crystallization commenced at T  gt  640 degrees C with high homogeneous nucleation rate and spherulite crystal growth morphology. DTA curves recorded for powder samples particle size  lt  0.1 mm revealed three exothermic peaks and three endothermic peaks within temperature range of T = 640-940 degrees C, while the DTA curves recorded for powder samples particle size  gt  0.1 mm showed two exothermic peaks and two endothermic peaks within temperature range of T = 640-1020 degrees C. The analysis of the dominant crystallization mechanism of powder glass sample and kinetics of crystallization is presented.",
publisher = "University of Chemistry and Technology, Prague",
journal = "Ceramics - Silikaty",
title = "The crystallization of potassium germanate glass with high content of niobium oxide",
pages = "68-61",
number = "1",
volume = "56",
url = "https://hdl.handle.net/21.15107/rcub_technorep_1981"
}
Matijašević, S. D., Tošić, M. B., Stojanović, J., Grujić, S., Živanović, V. D., Nikolić, J. D.,& Đošić, M.. (2012). The crystallization of potassium germanate glass with high content of niobium oxide. in Ceramics - Silikaty
University of Chemistry and Technology, Prague., 56(1), 61-68.
https://hdl.handle.net/21.15107/rcub_technorep_1981
Matijašević SD, Tošić MB, Stojanović J, Grujić S, Živanović VD, Nikolić JD, Đošić M. The crystallization of potassium germanate glass with high content of niobium oxide. in Ceramics - Silikaty. 2012;56(1):61-68.
https://hdl.handle.net/21.15107/rcub_technorep_1981 .
Matijašević, Srđan D., Tošić, Mihajlo B., Stojanović, Jovica, Grujić, Snežana, Živanović, Vladimir D., Nikolić, Jelena D., Đošić, Marija, "The crystallization of potassium germanate glass with high content of niobium oxide" in Ceramics - Silikaty, 56, no. 1 (2012):61-68,
https://hdl.handle.net/21.15107/rcub_technorep_1981 .
2

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

Đošić, Marija; Panić, V.; Stojanović, Jovica; Mitrić, Miodrag; Mišković-Stanković, Vesna

(Elsevier, Amsterdam, 2012)

TY  - JOUR
AU  - Đošić, Marija
AU  - Panić, V.
AU  - Stojanović, Jovica
AU  - Mitrić, Miodrag
AU  - Mišković-Stanković, Vesna
PY  - 2012
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/2246
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.
PB  - Elsevier, Amsterdam
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
EP  - 43
SP  - 36
VL  - 400
DO  - 10.1016/j.colsurfa.2012.02.040
ER  - 
@article{
author = "Đošić, Marija and Panić, V. and Stojanović, Jovica and Mitrić, Miodrag and Mišković-Stanković, Vesna",
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.",
publisher = "Elsevier, Amsterdam",
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",
pages = "43-36",
volume = "400",
doi = "10.1016/j.colsurfa.2012.02.040"
}
Đošić, M., Panić, V., Stojanović, J., Mitrić, M.,& Mišković-Stanković, V.. (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
Elsevier, Amsterdam., 400, 36-43.
https://doi.org/10.1016/j.colsurfa.2012.02.040
Đošić M, Panić V, Stojanović J, Mitrić M, Mišković-Stanković V. 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 .
Đošić, Marija, Panić, V., Stojanović, Jovica, Mitrić, Miodrag, Mišković-Stanković, Vesna, "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 . .
46
41
50

The effect of K2O on the crystallization of niobium germanate glasses

Matijašević, Srđan D.; Tošić, Mihajlo B.; Grujić, Snežana; Stojanović, Jovica; Živanović, Vladimir D.; Nikolić, J. D.

(International Institute for the Science of Sintering, Beograd, 2011)

TY  - JOUR
AU  - Matijašević, Srđan D.
AU  - Tošić, Mihajlo B.
AU  - Grujić, Snežana
AU  - Stojanović, Jovica
AU  - Živanović, Vladimir D.
AU  - Nikolić, J. D.
PY  - 2011
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1832
AB  - The effect of K2O content on the crystallization of niobium germanate glasses with 22.7- 24.27 wt% of GeO2 and 54.59-57.48 wt% of Nb2O5 was examined. The glasses crystallize by primary crystallization and the formed crystalline phases were K6Nb6Ge4O26, K3.8Nb5Ge3O20.4 and KNbO3. Increasing the K2O content caused a decrease in the GeO2 content of the primary phases. The effect of the K2O content on the kinetics of primary crystallization was analyzed. It was demonstrated that an increase of the K2O content decreased the activation energy of crystal growth at first of the crystallization peaks (Ec1). At second crystallization peaks the activation energies of crystal growth increased (Ec2).
AB  - Ispitan je uticaj sadržaja K2O na kristalizaciju niobijum germanatnih stakala sa 22,7-24,27 mas % GeO2 i 54,59-57,48 mas % Nb2O5. Ova stakla kristališu primarnom kristalizacijom i stvaraju se kristalne faze K6Nb6Ge4O26, K3.8Nb5Ge3O20.4 i KNbO3. Povećanje sadržaja K2O prouzrokuje smanjenje sadržaja GeO2 u primarnim fazama. Analiziran je uticaj sadržaja K2O na kinetiku primarne kristalizacije. Pokazano je da povećanje sadržaja K2O smanjuje energiju aktivacije rasta kristala na prvom kristalizacionom piku (Ec1). Na drugom kristalizacionom piku energije aktivacije rasta kristala se povećavaju (Ec2).
PB  - International Institute for the Science of Sintering, Beograd
T2  - Science of Sintering
T1  - The effect of K2O on the crystallization of niobium germanate glasses
EP  - 53
IS  - 1
SP  - 47
VL  - 43
UR  - https://hdl.handle.net/21.15107/rcub_technorep_1832
ER  - 
@article{
author = "Matijašević, Srđan D. and Tošić, Mihajlo B. and Grujić, Snežana and Stojanović, Jovica and Živanović, Vladimir D. and Nikolić, J. D.",
year = "2011",
abstract = "The effect of K2O content on the crystallization of niobium germanate glasses with 22.7- 24.27 wt% of GeO2 and 54.59-57.48 wt% of Nb2O5 was examined. The glasses crystallize by primary crystallization and the formed crystalline phases were K6Nb6Ge4O26, K3.8Nb5Ge3O20.4 and KNbO3. Increasing the K2O content caused a decrease in the GeO2 content of the primary phases. The effect of the K2O content on the kinetics of primary crystallization was analyzed. It was demonstrated that an increase of the K2O content decreased the activation energy of crystal growth at first of the crystallization peaks (Ec1). At second crystallization peaks the activation energies of crystal growth increased (Ec2)., Ispitan je uticaj sadržaja K2O na kristalizaciju niobijum germanatnih stakala sa 22,7-24,27 mas % GeO2 i 54,59-57,48 mas % Nb2O5. Ova stakla kristališu primarnom kristalizacijom i stvaraju se kristalne faze K6Nb6Ge4O26, K3.8Nb5Ge3O20.4 i KNbO3. Povećanje sadržaja K2O prouzrokuje smanjenje sadržaja GeO2 u primarnim fazama. Analiziran je uticaj sadržaja K2O na kinetiku primarne kristalizacije. Pokazano je da povećanje sadržaja K2O smanjuje energiju aktivacije rasta kristala na prvom kristalizacionom piku (Ec1). Na drugom kristalizacionom piku energije aktivacije rasta kristala se povećavaju (Ec2).",
publisher = "International Institute for the Science of Sintering, Beograd",
journal = "Science of Sintering",
title = "The effect of K2O on the crystallization of niobium germanate glasses",
pages = "53-47",
number = "1",
volume = "43",
url = "https://hdl.handle.net/21.15107/rcub_technorep_1832"
}
Matijašević, S. D., Tošić, M. B., Grujić, S., Stojanović, J., Živanović, V. D.,& Nikolić, J. D.. (2011). The effect of K2O on the crystallization of niobium germanate glasses. in Science of Sintering
International Institute for the Science of Sintering, Beograd., 43(1), 47-53.
https://hdl.handle.net/21.15107/rcub_technorep_1832
Matijašević SD, Tošić MB, Grujić S, Stojanović J, Živanović VD, Nikolić JD. The effect of K2O on the crystallization of niobium germanate glasses. in Science of Sintering. 2011;43(1):47-53.
https://hdl.handle.net/21.15107/rcub_technorep_1832 .
Matijašević, Srđan D., Tošić, Mihajlo B., Grujić, Snežana, Stojanović, Jovica, Živanović, Vladimir D., Nikolić, J. D., "The effect of K2O on the crystallization of niobium germanate glasses" in Science of Sintering, 43, no. 1 (2011):47-53,
https://hdl.handle.net/21.15107/rcub_technorep_1832 .
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4

Crystallization behaviour of Li2O·Nb2O5·SiO2 glass containing TiO2

Matijašević, Srđan D.; Živanović, Vladimir D.; Tošić, Mihajlo B.; Grujić, Snežana; Stojanović, Jovica; Nikolić, Jelena D.; Ždrale, Sonja V.

(University of Novi Sad, 2011)

TY  - JOUR
AU  - Matijašević, Srđan D.
AU  - Živanović, Vladimir D.
AU  - Tošić, Mihajlo B.
AU  - Grujić, Snežana
AU  - Stojanović, Jovica
AU  - Nikolić, Jelena D.
AU  - Ždrale, Sonja V.
PY  - 2011
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1821
AB  - This paper deals with the crystallization of glass 30Li2O·15Nb2O5·50SiO2·5TiO2 (mol%). The crystallization behavior was studied under isothermal and non-isothermal conditions. XRD and SEM methods were employed for determination of phase composition and microstructure of crystallized glass. It was detected that this glass crystallizes by the surface crystallization mechanism. SEM micrographs of the crystallized samples revealed that the crystals grow in the form of dendrites. The glass-ceramics with complex phase composition was obtained. Three crystalline phases were detected where LiNbO3 has grown as primary phase and a secondary ones Li2Si2O5 and SiO2 appeared. The calculated average crystallite sizes are: 27 nm for LiNbO3 , 115 nm for Li2Si2O5 and 45 nm for SiO2 . From the experimental data an activation energy of crystals growth, calculated using the Kissinger relation, is Ea = 275 ±10 KJ / mol.
PB  - University of Novi Sad
T2  - Processing and Application of Ceramics
T1  - Crystallization behaviour of Li2O·Nb2O5·SiO2 glass containing TiO2
EP  - 227
IS  - 4
SP  - 223
VL  - 5
UR  - https://hdl.handle.net/21.15107/rcub_technorep_1821
ER  - 
@article{
author = "Matijašević, Srđan D. and Živanović, Vladimir D. and Tošić, Mihajlo B. and Grujić, Snežana and Stojanović, Jovica and Nikolić, Jelena D. and Ždrale, Sonja V.",
year = "2011",
abstract = "This paper deals with the crystallization of glass 30Li2O·15Nb2O5·50SiO2·5TiO2 (mol%). The crystallization behavior was studied under isothermal and non-isothermal conditions. XRD and SEM methods were employed for determination of phase composition and microstructure of crystallized glass. It was detected that this glass crystallizes by the surface crystallization mechanism. SEM micrographs of the crystallized samples revealed that the crystals grow in the form of dendrites. The glass-ceramics with complex phase composition was obtained. Three crystalline phases were detected where LiNbO3 has grown as primary phase and a secondary ones Li2Si2O5 and SiO2 appeared. The calculated average crystallite sizes are: 27 nm for LiNbO3 , 115 nm for Li2Si2O5 and 45 nm for SiO2 . From the experimental data an activation energy of crystals growth, calculated using the Kissinger relation, is Ea = 275 ±10 KJ / mol.",
publisher = "University of Novi Sad",
journal = "Processing and Application of Ceramics",
title = "Crystallization behaviour of Li2O·Nb2O5·SiO2 glass containing TiO2",
pages = "227-223",
number = "4",
volume = "5",
url = "https://hdl.handle.net/21.15107/rcub_technorep_1821"
}
Matijašević, S. D., Živanović, V. D., Tošić, M. B., Grujić, S., Stojanović, J., Nikolić, J. D.,& Ždrale, S. V.. (2011). Crystallization behaviour of Li2O·Nb2O5·SiO2 glass containing TiO2. in Processing and Application of Ceramics
University of Novi Sad., 5(4), 223-227.
https://hdl.handle.net/21.15107/rcub_technorep_1821
Matijašević SD, Živanović VD, Tošić MB, Grujić S, Stojanović J, Nikolić JD, Ždrale SV. Crystallization behaviour of Li2O·Nb2O5·SiO2 glass containing TiO2. in Processing and Application of Ceramics. 2011;5(4):223-227.
https://hdl.handle.net/21.15107/rcub_technorep_1821 .
Matijašević, Srđan D., Živanović, Vladimir D., Tošić, Mihajlo B., Grujić, Snežana, Stojanović, Jovica, Nikolić, Jelena D., Ždrale, Sonja V., "Crystallization behaviour of Li2O·Nb2O5·SiO2 glass containing TiO2" in Processing and Application of Ceramics, 5, no. 4 (2011):223-227,
https://hdl.handle.net/21.15107/rcub_technorep_1821 .

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

Đošić, Marija; Mišković-Stanković, Vesna; Kačarević-Popović, Zorica M.; Jokić, Bojan; Bibić, Nataša M.; Mitrić, Miodrag; Milonjić, Slobodan K.; Jančić-Heinemann, Radmila; Stojanović, Jovica

(Elsevier Science Bv, Amsterdam, 2009)

TY  - JOUR
AU  - Đošić, Marija
AU  - Mišković-Stanković, Vesna
AU  - Kačarević-Popović, Zorica M.
AU  - Jokić, Bojan
AU  - Bibić, Nataša M.
AU  - Mitrić, Miodrag
AU  - Milonjić, Slobodan K.
AU  - Jančić-Heinemann, Radmila
AU  - Stojanović, Jovica
PY  - 2009
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1514
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.
PB  - Elsevier Science Bv, Amsterdam
T2  - Colloids and Surfaces A-Physicochemical and Engineering Aspects
T1  - Electrochemical synthesis of nanosized monetite powder and its electrophoretic deposition on titanium
EP  - 117
IS  - 1-3
SP  - 110
VL  - 341
DO  - 10.1016/j.colsurfa.2009.03.046
ER  - 
@article{
author = "Đošić, Marija and Mišković-Stanković, Vesna and Kačarević-Popović, Zorica M. and Jokić, Bojan and Bibić, Nataša M. and Mitrić, Miodrag and Milonjić, Slobodan K. and Jančić-Heinemann, Radmila and Stojanović, Jovica",
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.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Colloids and Surfaces A-Physicochemical and Engineering Aspects",
title = "Electrochemical synthesis of nanosized monetite powder and its electrophoretic deposition on titanium",
pages = "117-110",
number = "1-3",
volume = "341",
doi = "10.1016/j.colsurfa.2009.03.046"
}
Đošić, M., Mišković-Stanković, V., Kačarević-Popović, Z. M., Jokić, B., Bibić, N. M., Mitrić, M., Milonjić, S. K., Jančić-Heinemann, R.,& Stojanović, J.. (2009). Electrochemical synthesis of nanosized monetite powder and its electrophoretic deposition on titanium. in Colloids and Surfaces A-Physicochemical and Engineering Aspects
Elsevier Science Bv, Amsterdam., 341(1-3), 110-117.
https://doi.org/10.1016/j.colsurfa.2009.03.046
Đošić M, Mišković-Stanković V, Kačarević-Popović ZM, Jokić B, Bibić NM, Mitrić M, Milonjić SK, Jančić-Heinemann R, Stojanović 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 .
Đošić, Marija, Mišković-Stanković, Vesna, Kačarević-Popović, Zorica M., Jokić, Bojan, Bibić, Nataša M., Mitrić, Miodrag, Milonjić, Slobodan K., Jančić-Heinemann, Radmila, Stojanović, Jovica, "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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62

Electrodeposited hydroxyapatite thin films modified by ion beam irradiation

Đošić, Marija; Bibić, Nataša M.; Mitrić, Miodrag; Šiljegović, Milorad; Stojanović, Jovica; Jokić, Bojan; Janaćković, Đorđe; Mišković-Stanković, Vesna

(Natl Inst Optoelectronics, Bucharest-Magurele, 2009)

TY  - JOUR
AU  - Đošić, Marija
AU  - Bibić, Nataša M.
AU  - Mitrić, Miodrag
AU  - Šiljegović, Milorad
AU  - Stojanović, Jovica
AU  - Jokić, Bojan
AU  - Janaćković, Đorđe
AU  - Mišković-Stanković, Vesna
PY  - 2009
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1531
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 N4+ 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 Ar6+ 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.
PB  - Natl Inst Optoelectronics, Bucharest-Magurele
T2  - Journal of Optoelectronics and Advanced Materials
T1  - Electrodeposited hydroxyapatite thin films modified by ion beam irradiation
EP  - 1854
IS  - 11
SP  - 1848
VL  - 11
UR  - https://hdl.handle.net/21.15107/rcub_vinar_3872
ER  - 
@article{
author = "Đošić, Marija and Bibić, Nataša M. and Mitrić, Miodrag and Šiljegović, Milorad and Stojanović, Jovica and Jokić, Bojan and Janaćković, Đorđe and Mišković-Stanković, Vesna",
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 N4+ 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 Ar6+ 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.",
publisher = "Natl Inst Optoelectronics, Bucharest-Magurele",
journal = "Journal of Optoelectronics and Advanced Materials",
title = "Electrodeposited hydroxyapatite thin films modified by ion beam irradiation",
pages = "1854-1848",
number = "11",
volume = "11",
url = "https://hdl.handle.net/21.15107/rcub_vinar_3872"
}
Đošić, M., Bibić, N. M., Mitrić, M., Šiljegović, M., Stojanović, J., Jokić, B., Janaćković, Đ.,& Mišković-Stanković, V.. (2009). Electrodeposited hydroxyapatite thin films modified by ion beam irradiation. in Journal of Optoelectronics and Advanced Materials
Natl Inst Optoelectronics, Bucharest-Magurele., 11(11), 1848-1854.
https://hdl.handle.net/21.15107/rcub_vinar_3872
Đošić M, Bibić NM, Mitrić M, Šiljegović M, Stojanović J, Jokić B, Janaćković Đ, Mišković-Stanković V. 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 .
Đošić, Marija, Bibić, Nataša M., Mitrić, Miodrag, Šiljegović, Milorad, Stojanović, Jovica, Jokić, Bojan, Janaćković, Đorđe, Mišković-Stanković, Vesna, "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 .
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6