Lončarević, Davor

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orcid::0000-0002-2266-337X
  • Lončarević, Davor (19)
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Author's Bibliography

Photocatalytic hydrogen evolution over surface-modified titanate nanotubes by 5-aminosalicylic acid decorated with silver nanoparticles

Barbieriková, Zuzana; Lončarević, Davor; Papan, Jelena; Vukoje, Ivana D.; Stoiljković, Milovan; Ahrenkiel, Scott Phillip; Nedeljković, Jovan

(Elsevier B.V. and The Society of Powder Technology Japan, 2020)

TY  - JOUR
AU  - Barbieriková, Zuzana
AU  - Lončarević, Davor
AU  - Papan, Jelena
AU  - Vukoje, Ivana D.
AU  - Stoiljković, Milovan
AU  - Ahrenkiel, Scott Phillip
AU  - Nedeljković, Jovan
PY  - 2020
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/9756
AB  - The efficiency of titanate-nanotubes-based photocatalysts towards hydrogen production was studied in the presence of the sacrificial agent, 2-propanol. The highest hydrogen production rate (~120 lmol h 1 g 1 ) was observed over surface-modified titanate nanotubes by 5-amino salicylic acid decorated with nanometer-sized silver nanoparticles. The X-ray diffraction analysis, transmission electron microscopy, nitrogen adsorption–desorption isotherms, and diffuse reflection spectroscopy were applied to characterize the prepared photocatalytic materials. The better photocatalytic performance of inorganic–organic hybrid materials in comparison to the pristine titanate nanotubes is a consequence of their improved light-harvesting ability due to the formation of interfacial charge transfer (ICT) complex, as well as the presence of metallic silver nanoparticles that suppress the recombination of photo-generated charge carriers. The spin trapping EPR experiments under irradiation of prepared photocatalysts with either UV or visible light were used to monitor the appearance of hydroxyl radicals and superoxide radical anions. The generation of superoxide radical anions under visible light irradiation was detected for hybrid materials, but not for the pristine titanate nanotubes. These results are a consequence of enhanced promotion ofelectrons to the conduction band due to extended absorption in visible spectral range in hybrids and support the higher efficiency of hydrogen generation observed for surface-modified titanate nanotubes by 5-amino salicylic acid decorated with silver nanoparticles.
PB  - Elsevier B.V. and The Society of Powder Technology Japan
T2  - Advanced Powder Technology
T1  - Photocatalytic hydrogen evolution over surface-modified titanate nanotubes by 5-aminosalicylic acid decorated with silver nanoparticles
VL  - 31
IS  - 12
SP  - 4683
EP  - 4690
DO  - 10.1016/j.apt.2020.11.001
ER  - 
@article{
author = "Barbieriková, Zuzana and Lončarević, Davor and Papan, Jelena and Vukoje, Ivana D. and Stoiljković, Milovan and Ahrenkiel, Scott Phillip and Nedeljković, Jovan",
year = "2020",
abstract = "The efficiency of titanate-nanotubes-based photocatalysts towards hydrogen production was studied in the presence of the sacrificial agent, 2-propanol. The highest hydrogen production rate (~120 lmol h 1 g 1 ) was observed over surface-modified titanate nanotubes by 5-amino salicylic acid decorated with nanometer-sized silver nanoparticles. The X-ray diffraction analysis, transmission electron microscopy, nitrogen adsorption–desorption isotherms, and diffuse reflection spectroscopy were applied to characterize the prepared photocatalytic materials. The better photocatalytic performance of inorganic–organic hybrid materials in comparison to the pristine titanate nanotubes is a consequence of their improved light-harvesting ability due to the formation of interfacial charge transfer (ICT) complex, as well as the presence of metallic silver nanoparticles that suppress the recombination of photo-generated charge carriers. The spin trapping EPR experiments under irradiation of prepared photocatalysts with either UV or visible light were used to monitor the appearance of hydroxyl radicals and superoxide radical anions. The generation of superoxide radical anions under visible light irradiation was detected for hybrid materials, but not for the pristine titanate nanotubes. These results are a consequence of enhanced promotion ofelectrons to the conduction band due to extended absorption in visible spectral range in hybrids and support the higher efficiency of hydrogen generation observed for surface-modified titanate nanotubes by 5-amino salicylic acid decorated with silver nanoparticles.",
publisher = "Elsevier B.V. and The Society of Powder Technology Japan",
journal = "Advanced Powder Technology",
title = "Photocatalytic hydrogen evolution over surface-modified titanate nanotubes by 5-aminosalicylic acid decorated with silver nanoparticles",
volume = "31",
number = "12",
pages = "4683-4690",
doi = "10.1016/j.apt.2020.11.001"
}
Barbieriková, Z., Lončarević, D., Papan, J., Vukoje, I. D., Stoiljković, M., Ahrenkiel, S. P.,& Nedeljković, J.. (2020). Photocatalytic hydrogen evolution over surface-modified titanate nanotubes by 5-aminosalicylic acid decorated with silver nanoparticles. in Advanced Powder Technology
Elsevier B.V. and The Society of Powder Technology Japan., 31(12), 4683-4690.
https://doi.org/10.1016/j.apt.2020.11.001
Barbieriková Z, Lončarević D, Papan J, Vukoje ID, Stoiljković M, Ahrenkiel SP, Nedeljković J. Photocatalytic hydrogen evolution over surface-modified titanate nanotubes by 5-aminosalicylic acid decorated with silver nanoparticles. in Advanced Powder Technology. 2020;31(12):4683-4690.
doi:10.1016/j.apt.2020.11.001 .
Barbieriková, Zuzana, Lončarević, Davor, Papan, Jelena, Vukoje, Ivana D., Stoiljković, Milovan, Ahrenkiel, Scott Phillip, Nedeljković, Jovan, "Photocatalytic hydrogen evolution over surface-modified titanate nanotubes by 5-aminosalicylic acid decorated with silver nanoparticles" in Advanced Powder Technology, 31, no. 12 (2020):4683-4690,
https://doi.org/10.1016/j.apt.2020.11.001 . .

Visible light absorption of surface-modified Al2O3 powders: A comparative DFT and experimental study

Đorđević, Vesna R.; Sredojević, Dušan; Dostanić, Jasmina; Lončarević, Davor; Ahrenkiel, Scott Phillip; Švrakić, Nenad M.; Brothers, Edward N.; Belić, Milivoj R.; Nedeljković, Jovan

(2019)

TY  - JOUR
AU  - Đorđević, Vesna R.
AU  - Sredojević, Dušan
AU  - Dostanić, Jasmina
AU  - Lončarević, Davor
AU  - Ahrenkiel, Scott Phillip
AU  - Švrakić, Nenad M.
AU  - Brothers, Edward N.
AU  - Belić, Milivoj R.
AU  - Nedeljković, Jovan
PY  - 2019
UR  - https://linkinghub.elsevier.com/retrieve/pii/S1387181118303639
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7763
AB  - Surface modification of Al2O3 powders, prepared using reproducible sol-gel synthetic route with small colorless organic molecules, induces charge transfer complex formation and the appearance of absorption in the visible spectral region. Comprehensive microstructural characterization involving transmission electron microscopy, X-ray diffraction analysis, and nitrogen adsorption–desorption isotherms, revealed that γ-crystalline alumina powders consist of mesoporous particles in the size range from 0.1 to 0.3 μm, with specific surface area of 54.8 m2/g, and pore radius between 3 and 4 nm. The attachment of catecholate-type of ligands (catechol, caffeic acid, gallic acid, dopamine and 2,3-dihydroxy naphthalene), salicylate-type of ligands (salicylic acid and 5-amino salicylic acid), and ascorbic acid, to the surface such γ-Al2O3 particles leads to the formation of colored powders and activates their absorption in visible-light spectral region. To the best of our knowledge, similar transformation of an insulator (Al2O3), with the band gap energy of 8.7 eV, into a semiconductor-like hybrid material with tunable optical properties has not been reported in the literature before. The density functional theory (DFT) calculations with periodic boundary conditions were performed in order to estimate the energy gaps of various inorganic/organic hybrids. The calculated values compare well with the experimental data. The good agreement between the calculated and experimentally determined band gaps was found, thus demonstrating predictive ability of the theory when proper model is used.
T2  - Microporous and Mesoporous Materials
T1  - Visible light absorption of surface-modified Al2O3 powders: A comparative DFT and experimental study
VL  - 273
SP  - 41
EP  - 49
DO  - 10.1016/j.micromeso.2018.06.053
ER  - 
@article{
author = "Đorđević, Vesna R. and Sredojević, Dušan and Dostanić, Jasmina and Lončarević, Davor and Ahrenkiel, Scott Phillip and Švrakić, Nenad M. and Brothers, Edward N. and Belić, Milivoj R. and Nedeljković, Jovan",
year = "2019",
abstract = "Surface modification of Al2O3 powders, prepared using reproducible sol-gel synthetic route with small colorless organic molecules, induces charge transfer complex formation and the appearance of absorption in the visible spectral region. Comprehensive microstructural characterization involving transmission electron microscopy, X-ray diffraction analysis, and nitrogen adsorption–desorption isotherms, revealed that γ-crystalline alumina powders consist of mesoporous particles in the size range from 0.1 to 0.3 μm, with specific surface area of 54.8 m2/g, and pore radius between 3 and 4 nm. The attachment of catecholate-type of ligands (catechol, caffeic acid, gallic acid, dopamine and 2,3-dihydroxy naphthalene), salicylate-type of ligands (salicylic acid and 5-amino salicylic acid), and ascorbic acid, to the surface such γ-Al2O3 particles leads to the formation of colored powders and activates their absorption in visible-light spectral region. To the best of our knowledge, similar transformation of an insulator (Al2O3), with the band gap energy of 8.7 eV, into a semiconductor-like hybrid material with tunable optical properties has not been reported in the literature before. The density functional theory (DFT) calculations with periodic boundary conditions were performed in order to estimate the energy gaps of various inorganic/organic hybrids. The calculated values compare well with the experimental data. The good agreement between the calculated and experimentally determined band gaps was found, thus demonstrating predictive ability of the theory when proper model is used.",
journal = "Microporous and Mesoporous Materials",
title = "Visible light absorption of surface-modified Al2O3 powders: A comparative DFT and experimental study",
volume = "273",
pages = "41-49",
doi = "10.1016/j.micromeso.2018.06.053"
}
Đorđević, V. R., Sredojević, D., Dostanić, J., Lončarević, D., Ahrenkiel, S. P., Švrakić, N. M., Brothers, E. N., Belić, M. R.,& Nedeljković, J.. (2019). Visible light absorption of surface-modified Al2O3 powders: A comparative DFT and experimental study. in Microporous and Mesoporous Materials, 273, 41-49.
https://doi.org/10.1016/j.micromeso.2018.06.053
Đorđević VR, Sredojević D, Dostanić J, Lončarević D, Ahrenkiel SP, Švrakić NM, Brothers EN, Belić MR, Nedeljković J. Visible light absorption of surface-modified Al2O3 powders: A comparative DFT and experimental study. in Microporous and Mesoporous Materials. 2019;273:41-49.
doi:10.1016/j.micromeso.2018.06.053 .
Đorđević, Vesna R., Sredojević, Dušan, Dostanić, Jasmina, Lončarević, Davor, Ahrenkiel, Scott Phillip, Švrakić, Nenad M., Brothers, Edward N., Belić, Milivoj R., Nedeljković, Jovan, "Visible light absorption of surface-modified Al2O3 powders: A comparative DFT and experimental study" in Microporous and Mesoporous Materials, 273 (2019):41-49,
https://doi.org/10.1016/j.micromeso.2018.06.053 . .
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8
8

Efficient photocatalytic hydrogen production over titanate/titania nanostructures modified with nickel

Dostanić, Jasmina; Lončarević, Davor; Pavlović, Vladimir B.; Papan, Jelena; Nedeljković, Jovan

(2019)

TY  - JOUR
AU  - Dostanić, Jasmina
AU  - Lončarević, Davor
AU  - Pavlović, Vladimir B.
AU  - Papan, Jelena
AU  - Nedeljković, Jovan
PY  - 2019
UR  - https://linkinghub.elsevier.com/retrieve/pii/S0272884219317018
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8354
AB  - Nickel-modified titanate/TiO2 catalysts were prepared by deposition of nickel ions onto hydrothermally prepared titanate supports, followed by hydrogen temperature-programmed reduction. Two different nickel precursors (hydroxide and carbonate) were used to tune reducibility and to vary the crystal phase structure of the final catalysts. The precursor reducibility and functional properties of the final catalysts were investigated systematically using various characterisation techniques. The results revealed a more facile reduction of the hydroxide precursor compared to its carbonate counterpart. Moreover, it was found that the formation of the anatase phase was favoured by the use of the hydroxide precipitation agent. The photocatalytic activity towards hydrogen production of the prepared catalysts was evaluated in the presence of 2-propanol under simulated solar light irradiation. A thorough study of the photocatalytic performance of the synthesised catalysts was conducted as a function of the precipitation agent used and the reduction temperature applied. The catalyst with dominant anatase crystal phase displayed the highest photocatalytic activity with a maximum H2 production rate of 1040 μmol h−1 g−1, this being more than four times higher than that of its carbonate counterpart. The catalysts with titanate structure showed similar activity, independent of the precipitation method used. The nanotubular structure was found to be the dominant factor in the stability of photocatalysts under long-run working conditions. © 2019 Elsevier Ltd and Techna Group S.r.l.
T2  - Ceramics International
T1  - Efficient photocatalytic hydrogen production over titanate/titania nanostructures modified with nickel
VL  - 45
IS  - 15
SP  - 19447
EP  - 19455
DO  - 10.1016/j.ceramint.2019.06.200
ER  - 
@article{
author = "Dostanić, Jasmina and Lončarević, Davor and Pavlović, Vladimir B. and Papan, Jelena and Nedeljković, Jovan",
year = "2019",
abstract = "Nickel-modified titanate/TiO2 catalysts were prepared by deposition of nickel ions onto hydrothermally prepared titanate supports, followed by hydrogen temperature-programmed reduction. Two different nickel precursors (hydroxide and carbonate) were used to tune reducibility and to vary the crystal phase structure of the final catalysts. The precursor reducibility and functional properties of the final catalysts were investigated systematically using various characterisation techniques. The results revealed a more facile reduction of the hydroxide precursor compared to its carbonate counterpart. Moreover, it was found that the formation of the anatase phase was favoured by the use of the hydroxide precipitation agent. The photocatalytic activity towards hydrogen production of the prepared catalysts was evaluated in the presence of 2-propanol under simulated solar light irradiation. A thorough study of the photocatalytic performance of the synthesised catalysts was conducted as a function of the precipitation agent used and the reduction temperature applied. The catalyst with dominant anatase crystal phase displayed the highest photocatalytic activity with a maximum H2 production rate of 1040 μmol h−1 g−1, this being more than four times higher than that of its carbonate counterpart. The catalysts with titanate structure showed similar activity, independent of the precipitation method used. The nanotubular structure was found to be the dominant factor in the stability of photocatalysts under long-run working conditions. © 2019 Elsevier Ltd and Techna Group S.r.l.",
journal = "Ceramics International",
title = "Efficient photocatalytic hydrogen production over titanate/titania nanostructures modified with nickel",
volume = "45",
number = "15",
pages = "19447-19455",
doi = "10.1016/j.ceramint.2019.06.200"
}
Dostanić, J., Lončarević, D., Pavlović, V. B., Papan, J.,& Nedeljković, J.. (2019). Efficient photocatalytic hydrogen production over titanate/titania nanostructures modified with nickel. in Ceramics International, 45(15), 19447-19455.
https://doi.org/10.1016/j.ceramint.2019.06.200
Dostanić J, Lončarević D, Pavlović VB, Papan J, Nedeljković J. Efficient photocatalytic hydrogen production over titanate/titania nanostructures modified with nickel. in Ceramics International. 2019;45(15):19447-19455.
doi:10.1016/j.ceramint.2019.06.200 .
Dostanić, Jasmina, Lončarević, Davor, Pavlović, Vladimir B., Papan, Jelena, Nedeljković, Jovan, "Efficient photocatalytic hydrogen production over titanate/titania nanostructures modified with nickel" in Ceramics International, 45, no. 15 (2019):19447-19455,
https://doi.org/10.1016/j.ceramint.2019.06.200 . .
4
4
4

Electronic structure of surface complexes between CeO2 and benzene derivatives: A comparative experimental and DFT study

Prekajski-Đorđević, Marija D.; Vukoje, Ivana D.; Lazić, Vesna M.; Đorđević, Vesna R.; Sredojević, Dušan; Dostanić, Jasmina; Lončarević, Davor; Ahrenkiel, Scott Phillip; Belić, Milivoj R.; Nedeljković, Jovan

(2019)

TY  - JOUR
AU  - Prekajski-Đorđević, Marija D.
AU  - Vukoje, Ivana D.
AU  - Lazić, Vesna M.
AU  - Đorđević, Vesna R.
AU  - Sredojević, Dušan
AU  - Dostanić, Jasmina
AU  - Lončarević, Davor
AU  - Ahrenkiel, Scott Phillip
AU  - Belić, Milivoj R.
AU  - Nedeljković, Jovan
PY  - 2019
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8387
AB  - Surface modification of CeO2 nano-powder, synthesized by a self-propagating room temperature method with salicylate-type ligands (salicylic acid and 5-aminosalicylic acid) as well as catecholate-type ligands (catechol, 3,4-dihydroxybenzoic acid, caffeic acid and 2,3-dihydroxy naphthalene), induces the appearance of absorption in the visible spectral region due to the interfacial charge transfer (ICT) complex formation. Thorough characterization involving transmission electron microscopy, XRD analysis, and nitrogen adsorption-desorption isotherms, revealed that loosely agglomerated CeO2 particles of the size ranging from 2 to 4 nm have cubic fluorite structure and specific surface area of 140 m2/g. The attachment of salicylate- and catecholate-type of ligands to the surface of CeO2 powders leads to the formation of colored powders with tunable absorption in the visible spectral region. The density functional theory calculations with properly design model systems were performed to estimate the alignment of energy levels of various inorganic/organic hybrids. A reasonably good agreement between calculated values and experimental data was found. © 2019
T2  - Materials Chemistry and Physics
T1  - Electronic structure of surface complexes between CeO2 and benzene derivatives: A comparative experimental and DFT study
VL  - 236
SP  - 121816
DO  - 10.1016/j.matchemphys.2019.121816
ER  - 
@article{
author = "Prekajski-Đorđević, Marija D. and Vukoje, Ivana D. and Lazić, Vesna M. and Đorđević, Vesna R. and Sredojević, Dušan and Dostanić, Jasmina and Lončarević, Davor and Ahrenkiel, Scott Phillip and Belić, Milivoj R. and Nedeljković, Jovan",
year = "2019",
abstract = "Surface modification of CeO2 nano-powder, synthesized by a self-propagating room temperature method with salicylate-type ligands (salicylic acid and 5-aminosalicylic acid) as well as catecholate-type ligands (catechol, 3,4-dihydroxybenzoic acid, caffeic acid and 2,3-dihydroxy naphthalene), induces the appearance of absorption in the visible spectral region due to the interfacial charge transfer (ICT) complex formation. Thorough characterization involving transmission electron microscopy, XRD analysis, and nitrogen adsorption-desorption isotherms, revealed that loosely agglomerated CeO2 particles of the size ranging from 2 to 4 nm have cubic fluorite structure and specific surface area of 140 m2/g. The attachment of salicylate- and catecholate-type of ligands to the surface of CeO2 powders leads to the formation of colored powders with tunable absorption in the visible spectral region. The density functional theory calculations with properly design model systems were performed to estimate the alignment of energy levels of various inorganic/organic hybrids. A reasonably good agreement between calculated values and experimental data was found. © 2019",
journal = "Materials Chemistry and Physics",
title = "Electronic structure of surface complexes between CeO2 and benzene derivatives: A comparative experimental and DFT study",
volume = "236",
pages = "121816",
doi = "10.1016/j.matchemphys.2019.121816"
}
Prekajski-Đorđević, M. D., Vukoje, I. D., Lazić, V. M., Đorđević, V. R., Sredojević, D., Dostanić, J., Lončarević, D., Ahrenkiel, S. P., Belić, M. R.,& Nedeljković, J.. (2019). Electronic structure of surface complexes between CeO2 and benzene derivatives: A comparative experimental and DFT study. in Materials Chemistry and Physics, 236, 121816.
https://doi.org/10.1016/j.matchemphys.2019.121816
Prekajski-Đorđević MD, Vukoje ID, Lazić VM, Đorđević VR, Sredojević D, Dostanić J, Lončarević D, Ahrenkiel SP, Belić MR, Nedeljković J. Electronic structure of surface complexes between CeO2 and benzene derivatives: A comparative experimental and DFT study. in Materials Chemistry and Physics. 2019;236:121816.
doi:10.1016/j.matchemphys.2019.121816 .
Prekajski-Đorđević, Marija D., Vukoje, Ivana D., Lazić, Vesna M., Đorđević, Vesna R., Sredojević, Dušan, Dostanić, Jasmina, Lončarević, Davor, Ahrenkiel, Scott Phillip, Belić, Milivoj R., Nedeljković, Jovan, "Electronic structure of surface complexes between CeO2 and benzene derivatives: A comparative experimental and DFT study" in Materials Chemistry and Physics, 236 (2019):121816,
https://doi.org/10.1016/j.matchemphys.2019.121816 . .
3
3

Antibacterial ability of supported silver nanoparticles by functionalized hydroxyapatite with 5-aminosalicylic acid

Lazić, Vesna M.; Smičiklas, Ivana D.; Marković, Jelena P.; Lončarević, Davor; Dostanic, Jasmina; Ahrenkiel, Scott Phillip; Nedeljković, Jovan

(2018)

TY  - JOUR
AU  - Lazić, Vesna M.
AU  - Smičiklas, Ivana D.
AU  - Marković, Jelena P.
AU  - Lončarević, Davor
AU  - Dostanic, Jasmina
AU  - Ahrenkiel, Scott Phillip
AU  - Nedeljković, Jovan
PY  - 2018
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1928
AB  - Antimicrobial performance of silver nanoparticles supported by functionalized hydroxyapatite with 5-aminosalycile acid was tested against Gram-negative bacteria E. coli, Gram-positive bacteria S. aureus and yeast C. albicans. Thorough characterization of materials (electron microscopy, nitrogen adsorption desorption isotherms, diffuse reflectance spectroscopy) followed each step during the course of nanocomposite preparation. Synthesized powder consists of rod-like hydroxyapatite particles (40-60 x 10-20 nm, length x diameter) decorated with nano-sized spherical silver particles whose content in nanocomposite was found to be 1.9 wt.-%. Concentration- and time-dependent bacterial reduction data indicated that use of silver nanoparticles even at concentration as low as 1 mu g mL(-1) lead to complete reduction of both bacteria (E. coli and S. aureus). On the other hand, non-toxic behavior of nanocomposite in broad concentration range (0.05-2.0 mg mL(-1)) was found towards C albicans. Successful inactivation of E. coli and S. aureus in five repeated cycles proved that synthesized nanocomposite can perform under long-run working conditions. (C) 2017 Elsevier Ltd. All rights reserved.
T2  - Vacuum
T1  - Antibacterial ability of supported silver nanoparticles by functionalized hydroxyapatite with 5-aminosalicylic acid
VL  - 148
SP  - 62
EP  - 68
DO  - 10.1016/j.vacuum.2017.10.039
ER  - 
@article{
author = "Lazić, Vesna M. and Smičiklas, Ivana D. and Marković, Jelena P. and Lončarević, Davor and Dostanic, Jasmina and Ahrenkiel, Scott Phillip and Nedeljković, Jovan",
year = "2018",
abstract = "Antimicrobial performance of silver nanoparticles supported by functionalized hydroxyapatite with 5-aminosalycile acid was tested against Gram-negative bacteria E. coli, Gram-positive bacteria S. aureus and yeast C. albicans. Thorough characterization of materials (electron microscopy, nitrogen adsorption desorption isotherms, diffuse reflectance spectroscopy) followed each step during the course of nanocomposite preparation. Synthesized powder consists of rod-like hydroxyapatite particles (40-60 x 10-20 nm, length x diameter) decorated with nano-sized spherical silver particles whose content in nanocomposite was found to be 1.9 wt.-%. Concentration- and time-dependent bacterial reduction data indicated that use of silver nanoparticles even at concentration as low as 1 mu g mL(-1) lead to complete reduction of both bacteria (E. coli and S. aureus). On the other hand, non-toxic behavior of nanocomposite in broad concentration range (0.05-2.0 mg mL(-1)) was found towards C albicans. Successful inactivation of E. coli and S. aureus in five repeated cycles proved that synthesized nanocomposite can perform under long-run working conditions. (C) 2017 Elsevier Ltd. All rights reserved.",
journal = "Vacuum",
title = "Antibacterial ability of supported silver nanoparticles by functionalized hydroxyapatite with 5-aminosalicylic acid",
volume = "148",
pages = "62-68",
doi = "10.1016/j.vacuum.2017.10.039"
}
Lazić, V. M., Smičiklas, I. D., Marković, J. P., Lončarević, D., Dostanic, J., Ahrenkiel, S. P.,& Nedeljković, J.. (2018). Antibacterial ability of supported silver nanoparticles by functionalized hydroxyapatite with 5-aminosalicylic acid. in Vacuum, 148, 62-68.
https://doi.org/10.1016/j.vacuum.2017.10.039
Lazić VM, Smičiklas ID, Marković JP, Lončarević D, Dostanic J, Ahrenkiel SP, Nedeljković J. Antibacterial ability of supported silver nanoparticles by functionalized hydroxyapatite with 5-aminosalicylic acid. in Vacuum. 2018;148:62-68.
doi:10.1016/j.vacuum.2017.10.039 .
Lazić, Vesna M., Smičiklas, Ivana D., Marković, Jelena P., Lončarević, Davor, Dostanic, Jasmina, Ahrenkiel, Scott Phillip, Nedeljković, Jovan, "Antibacterial ability of supported silver nanoparticles by functionalized hydroxyapatite with 5-aminosalicylic acid" in Vacuum, 148 (2018):62-68,
https://doi.org/10.1016/j.vacuum.2017.10.039 . .
20
17
18

Charge-transfer complex formation between TiO2 nanoparticles and thiosalicylic acid: A comprehensive experimental and DFT study

Milićević, Bojana R.; Đorđević, Vesna R.; Lončarević, Davor; Dostanic, Jasmina M.; Ahrenkiel, Scott Phillip; Dramićanin, Miroslav; Sredojević, Dušan; Švrakić, Nenad M.; Nedeljković, Jovan

(2017)

TY  - JOUR
AU  - Milićević, Bojana R.
AU  - Đorđević, Vesna R.
AU  - Lončarević, Davor
AU  - Dostanic, Jasmina M.
AU  - Ahrenkiel, Scott Phillip
AU  - Dramićanin, Miroslav
AU  - Sredojević, Dušan
AU  - Švrakić, Nenad M.
AU  - Nedeljković, Jovan
PY  - 2017
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1815
AB  - Under normal conditions, titanium dioxide does not absorb visible light photons due to large band gap. Nevertheless, when titanium dioxide nanoparticles (TiO2 NPs) are surface-modified with thiosalicylic acid (TSA), their optical properties are altered owing to the formation of charge transfer complex that initiates absorption in the visible spectral range. Colloidal and sol-gel techniques were used to synthesize uniform TiO2 NPs of different sizes (average diameters in the range 4-15 nm), and effects of their subsequent modification by TSA molecules were compared with effect of modification of commercial Degussa TiO2 powder. Thorough microstructural characterization of TiO2 nanoparticulates was performed including transmission electron microscopy (TEM) and X-ray diffraction (XRD) analysis, as well as nitrogen adsorption-desorption isotherms. Optical measurements revealed that all surface-modified TiO2 samples with TSA have similar spectral features independent of their morphological differences, and, more importantly, absorption onset of modified TiO2 samples was found to be red-shifted by 1.0 eV compared to the unmodified ones. The mode of binding between TSA and surface Ti atoms was analyzed by infrared spectroscopy. Finally, the quantum chemical calculations, based on density functional theory, were performed to support optical characterization of surface-modified TiO2 with TSA. (C) 2017 Elsevier B.V. All rights reserved.
T2  - Optical Materials
T1  - Charge-transfer complex formation between TiO2 nanoparticles and thiosalicylic acid: A comprehensive experimental and DFT study
VL  - 73
SP  - 163
EP  - 171
DO  - 10.1016/j.optmat.2017.08.011
ER  - 
@article{
author = "Milićević, Bojana R. and Đorđević, Vesna R. and Lončarević, Davor and Dostanic, Jasmina M. and Ahrenkiel, Scott Phillip and Dramićanin, Miroslav and Sredojević, Dušan and Švrakić, Nenad M. and Nedeljković, Jovan",
year = "2017",
abstract = "Under normal conditions, titanium dioxide does not absorb visible light photons due to large band gap. Nevertheless, when titanium dioxide nanoparticles (TiO2 NPs) are surface-modified with thiosalicylic acid (TSA), their optical properties are altered owing to the formation of charge transfer complex that initiates absorption in the visible spectral range. Colloidal and sol-gel techniques were used to synthesize uniform TiO2 NPs of different sizes (average diameters in the range 4-15 nm), and effects of their subsequent modification by TSA molecules were compared with effect of modification of commercial Degussa TiO2 powder. Thorough microstructural characterization of TiO2 nanoparticulates was performed including transmission electron microscopy (TEM) and X-ray diffraction (XRD) analysis, as well as nitrogen adsorption-desorption isotherms. Optical measurements revealed that all surface-modified TiO2 samples with TSA have similar spectral features independent of their morphological differences, and, more importantly, absorption onset of modified TiO2 samples was found to be red-shifted by 1.0 eV compared to the unmodified ones. The mode of binding between TSA and surface Ti atoms was analyzed by infrared spectroscopy. Finally, the quantum chemical calculations, based on density functional theory, were performed to support optical characterization of surface-modified TiO2 with TSA. (C) 2017 Elsevier B.V. All rights reserved.",
journal = "Optical Materials",
title = "Charge-transfer complex formation between TiO2 nanoparticles and thiosalicylic acid: A comprehensive experimental and DFT study",
volume = "73",
pages = "163-171",
doi = "10.1016/j.optmat.2017.08.011"
}
Milićević, B. R., Đorđević, V. R., Lončarević, D., Dostanic, J. M., Ahrenkiel, S. P., Dramićanin, M., Sredojević, D., Švrakić, N. M.,& Nedeljković, J.. (2017). Charge-transfer complex formation between TiO2 nanoparticles and thiosalicylic acid: A comprehensive experimental and DFT study. in Optical Materials, 73, 163-171.
https://doi.org/10.1016/j.optmat.2017.08.011
Milićević BR, Đorđević VR, Lončarević D, Dostanic JM, Ahrenkiel SP, Dramićanin M, Sredojević D, Švrakić NM, Nedeljković J. Charge-transfer complex formation between TiO2 nanoparticles and thiosalicylic acid: A comprehensive experimental and DFT study. in Optical Materials. 2017;73:163-171.
doi:10.1016/j.optmat.2017.08.011 .
Milićević, Bojana R., Đorđević, Vesna R., Lončarević, Davor, Dostanic, Jasmina M., Ahrenkiel, Scott Phillip, Dramićanin, Miroslav, Sredojević, Dušan, Švrakić, Nenad M., Nedeljković, Jovan, "Charge-transfer complex formation between TiO2 nanoparticles and thiosalicylic acid: A comprehensive experimental and DFT study" in Optical Materials, 73 (2017):163-171,
https://doi.org/10.1016/j.optmat.2017.08.011 . .
7
8

Hybrid visible-light responsive Al2O3 particles

Đorđević, Vesna R.; Dostanic, Jasmina; Lončarević, Davor; Ahrenkiel, Scott Phillip; Sredojević, Dušan; Švrakić, Nenad M.; Belić, Milivoj R.; Nedeljković, Jovan

(2017)

TY  - JOUR
AU  - Đorđević, Vesna R.
AU  - Dostanic, Jasmina
AU  - Lončarević, Davor
AU  - Ahrenkiel, Scott Phillip
AU  - Sredojević, Dušan
AU  - Švrakić, Nenad M.
AU  - Belić, Milivoj R.
AU  - Nedeljković, Jovan
PY  - 2017
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1723
AB  - Detailed study of Al2O3, an insulator with the band gap of about 8.7 eV, and its different organic/inorganic charge transfer complexes with visible-light photo activity is presented. In particular, prepared Al2O3 particles of the size 0.1-0.3 mu m are coated with several organic complexes - the specific details for catecholate- and salicylate-type of ligands are described below - and the light absorption properties and photocatalytic activity of such hybrids are scrutinized and compared with those of other organic/inorganic hybrid materials previously studied. In addition, the obtained experimental results are supported with quantum chemical calculations based on density functional theory. (C) 2017 Elsevier B.V. All rights reserved.
T2  - Chemical Physics Letters
T1  - Hybrid visible-light responsive Al2O3 particles
VL  - 685
SP  - 416
EP  - 421
DO  - 10.1016/j.cplett.2017.08.012
ER  - 
@article{
author = "Đorđević, Vesna R. and Dostanic, Jasmina and Lončarević, Davor and Ahrenkiel, Scott Phillip and Sredojević, Dušan and Švrakić, Nenad M. and Belić, Milivoj R. and Nedeljković, Jovan",
year = "2017",
abstract = "Detailed study of Al2O3, an insulator with the band gap of about 8.7 eV, and its different organic/inorganic charge transfer complexes with visible-light photo activity is presented. In particular, prepared Al2O3 particles of the size 0.1-0.3 mu m are coated with several organic complexes - the specific details for catecholate- and salicylate-type of ligands are described below - and the light absorption properties and photocatalytic activity of such hybrids are scrutinized and compared with those of other organic/inorganic hybrid materials previously studied. In addition, the obtained experimental results are supported with quantum chemical calculations based on density functional theory. (C) 2017 Elsevier B.V. All rights reserved.",
journal = "Chemical Physics Letters",
title = "Hybrid visible-light responsive Al2O3 particles",
volume = "685",
pages = "416-421",
doi = "10.1016/j.cplett.2017.08.012"
}
Đorđević, V. R., Dostanic, J., Lončarević, D., Ahrenkiel, S. P., Sredojević, D., Švrakić, N. M., Belić, M. R.,& Nedeljković, J.. (2017). Hybrid visible-light responsive Al2O3 particles. in Chemical Physics Letters, 685, 416-421.
https://doi.org/10.1016/j.cplett.2017.08.012
Đorđević VR, Dostanic J, Lončarević D, Ahrenkiel SP, Sredojević D, Švrakić NM, Belić MR, Nedeljković J. Hybrid visible-light responsive Al2O3 particles. in Chemical Physics Letters. 2017;685:416-421.
doi:10.1016/j.cplett.2017.08.012 .
Đorđević, Vesna R., Dostanic, Jasmina, Lončarević, Davor, Ahrenkiel, Scott Phillip, Sredojević, Dušan, Švrakić, Nenad M., Belić, Milivoj R., Nedeljković, Jovan, "Hybrid visible-light responsive Al2O3 particles" in Chemical Physics Letters, 685 (2017):416-421,
https://doi.org/10.1016/j.cplett.2017.08.012 . .
10
8
9

Functionalized biogenic hydroxyapatite with 5-aminosalicylic acid - Sorbent for efficient separation of Pb2+ and Cu2+ ions

Smičiklas, Ivana D.; Papan, Jelena; Lazić, Vesna M.; Lončarević, Davor; Ahrenkiel, Scott Phillip; Nedeljković, Jovan

(2017)

TY  - JOUR
AU  - Smičiklas, Ivana D.
AU  - Papan, Jelena
AU  - Lazić, Vesna M.
AU  - Lončarević, Davor
AU  - Ahrenkiel, Scott Phillip
AU  - Nedeljković, Jovan
PY  - 2017
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1732
AB  - The biogenic hydroxyapatite (BHAP), obtained by proper treatment of bovine bones, was functionalized with 5-aminosalicylic acid (5-ASA). The coordination of 5-ASA to the surface of BHAP leads to the charge transfer (CT) complex formation accompanied with absorption in visible spectral range. The sorption ability of surface-modified BHAP with 5-ASA (5-ASA/BHAP) for removal of Pb2+ and Cu2+ ions from single-and bi-component solutions was compared with unmodified BHAP. The thorough characterization of both sorbents, BHAP and 5-ASA/BHAP, was performed including X-ray diffraction analysis (XRD), transmission electron microscopy (TEM), nitrogen adsorption-desorption isotherms, as well as diffuse reflection spectroscopy. Sorption kinetics and equilibriums for both ions (Pb2+ and Cu2+) by as-prepared BHAP and 5-ASA/BHAP are quite different. Functionalized sorbent demonstrated faster sorption kinetic and higher maximum sorption capacity for Pb2+ ions from bi-component solutions. From equimolar Pb2+ and Cu2+ mixture with a total concentration of 10-2 mol/L, 66% of Pb2+ was recovered using BHAP, while 97% using 5-ASA/BHAP. These preliminary data indicate potential applicability of properly functionalized hydroxyapatite for selective removal of heavy metal ions from contaminated water.
T2  - Journal of Environmental Chemical Engineering
T1  - Functionalized biogenic hydroxyapatite with 5-aminosalicylic acid - Sorbent for efficient separation of Pb2+ and Cu2+ ions
VL  - 5
IS  - 4
SP  - 3759
EP  - 3765
DO  - 10.1016/j.jece.2017.07.027
ER  - 
@article{
author = "Smičiklas, Ivana D. and Papan, Jelena and Lazić, Vesna M. and Lončarević, Davor and Ahrenkiel, Scott Phillip and Nedeljković, Jovan",
year = "2017",
abstract = "The biogenic hydroxyapatite (BHAP), obtained by proper treatment of bovine bones, was functionalized with 5-aminosalicylic acid (5-ASA). The coordination of 5-ASA to the surface of BHAP leads to the charge transfer (CT) complex formation accompanied with absorption in visible spectral range. The sorption ability of surface-modified BHAP with 5-ASA (5-ASA/BHAP) for removal of Pb2+ and Cu2+ ions from single-and bi-component solutions was compared with unmodified BHAP. The thorough characterization of both sorbents, BHAP and 5-ASA/BHAP, was performed including X-ray diffraction analysis (XRD), transmission electron microscopy (TEM), nitrogen adsorption-desorption isotherms, as well as diffuse reflection spectroscopy. Sorption kinetics and equilibriums for both ions (Pb2+ and Cu2+) by as-prepared BHAP and 5-ASA/BHAP are quite different. Functionalized sorbent demonstrated faster sorption kinetic and higher maximum sorption capacity for Pb2+ ions from bi-component solutions. From equimolar Pb2+ and Cu2+ mixture with a total concentration of 10-2 mol/L, 66% of Pb2+ was recovered using BHAP, while 97% using 5-ASA/BHAP. These preliminary data indicate potential applicability of properly functionalized hydroxyapatite for selective removal of heavy metal ions from contaminated water.",
journal = "Journal of Environmental Chemical Engineering",
title = "Functionalized biogenic hydroxyapatite with 5-aminosalicylic acid - Sorbent for efficient separation of Pb2+ and Cu2+ ions",
volume = "5",
number = "4",
pages = "3759-3765",
doi = "10.1016/j.jece.2017.07.027"
}
Smičiklas, I. D., Papan, J., Lazić, V. M., Lončarević, D., Ahrenkiel, S. P.,& Nedeljković, J.. (2017). Functionalized biogenic hydroxyapatite with 5-aminosalicylic acid - Sorbent for efficient separation of Pb2+ and Cu2+ ions. in Journal of Environmental Chemical Engineering, 5(4), 3759-3765.
https://doi.org/10.1016/j.jece.2017.07.027
Smičiklas ID, Papan J, Lazić VM, Lončarević D, Ahrenkiel SP, Nedeljković J. Functionalized biogenic hydroxyapatite with 5-aminosalicylic acid - Sorbent for efficient separation of Pb2+ and Cu2+ ions. in Journal of Environmental Chemical Engineering. 2017;5(4):3759-3765.
doi:10.1016/j.jece.2017.07.027 .
Smičiklas, Ivana D., Papan, Jelena, Lazić, Vesna M., Lončarević, Davor, Ahrenkiel, Scott Phillip, Nedeljković, Jovan, "Functionalized biogenic hydroxyapatite with 5-aminosalicylic acid - Sorbent for efficient separation of Pb2+ and Cu2+ ions" in Journal of Environmental Chemical Engineering, 5, no. 4 (2017):3759-3765,
https://doi.org/10.1016/j.jece.2017.07.027 . .
10
7
9

Synthesis, Characterization, and Antimicrobial Activity of Silver Nanoparticles on Poly(GMA-co-EGDMA) Polymer Support

Vukoje, Ivana D.; Džunuzović, Enis S.; Lončarević, Davor; Dimitrijević, Suzana I.; Ahrenkiel, Scott Phillip; Nedeljković, Jovan

(2017)

TY  - JOUR
AU  - Vukoje, Ivana D.
AU  - Džunuzović, Enis S.
AU  - Lončarević, Davor
AU  - Dimitrijević, Suzana I.
AU  - Ahrenkiel, Scott Phillip
AU  - Nedeljković, Jovan
PY  - 2017
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1361
AB  - Poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate) (poly(GMA-co-EGDMA) macroporous copolymer decorated with silver nanoparticles was prepared by a modification of poly(GMA-co-EGDMA) in the reaction with arginine, and consequent reduction of silver ions with amino groups. The mercury intrusion porosimetry, transmission electron microscopy, X-ray diffraction, UV-vis reflection spectroscopy, and inductively coupled plasma atomic emission measurements were used to characterize obtained composite. The coordination of silver nanoparticles to the poly(GMA-co-EGDMA) copolymer was studied using infrared spectroscopy. Time dependence and concentration dependence of the antimicrobial efficiency of composite were tested against Gram-negative bacteria Escherichia coli, Gram-positive bacteria Staphylococcus aureus, and fungus Candida albicans. The composite ensured maximum reduction of both bacteria, while the fungi reduction reached satisfactory 96.8%. Preliminary antimicrobial efficiency measurements using laboratory flow setup indicated potential applicability of composite for wastewater treatment. (C) 2015 Society of Plastics Engineers
T2  - Polymer Composites
T1  - Synthesis, Characterization, and Antimicrobial Activity of Silver Nanoparticles on Poly(GMA-co-EGDMA) Polymer Support
VL  - 38
IS  - 6
SP  - 1206
EP  - 1214
DO  - 10.1002/pc.23684
ER  - 
@article{
author = "Vukoje, Ivana D. and Džunuzović, Enis S. and Lončarević, Davor and Dimitrijević, Suzana I. and Ahrenkiel, Scott Phillip and Nedeljković, Jovan",
year = "2017",
abstract = "Poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate) (poly(GMA-co-EGDMA) macroporous copolymer decorated with silver nanoparticles was prepared by a modification of poly(GMA-co-EGDMA) in the reaction with arginine, and consequent reduction of silver ions with amino groups. The mercury intrusion porosimetry, transmission electron microscopy, X-ray diffraction, UV-vis reflection spectroscopy, and inductively coupled plasma atomic emission measurements were used to characterize obtained composite. The coordination of silver nanoparticles to the poly(GMA-co-EGDMA) copolymer was studied using infrared spectroscopy. Time dependence and concentration dependence of the antimicrobial efficiency of composite were tested against Gram-negative bacteria Escherichia coli, Gram-positive bacteria Staphylococcus aureus, and fungus Candida albicans. The composite ensured maximum reduction of both bacteria, while the fungi reduction reached satisfactory 96.8%. Preliminary antimicrobial efficiency measurements using laboratory flow setup indicated potential applicability of composite for wastewater treatment. (C) 2015 Society of Plastics Engineers",
journal = "Polymer Composites",
title = "Synthesis, Characterization, and Antimicrobial Activity of Silver Nanoparticles on Poly(GMA-co-EGDMA) Polymer Support",
volume = "38",
number = "6",
pages = "1206-1214",
doi = "10.1002/pc.23684"
}
Vukoje, I. D., Džunuzović, E. S., Lončarević, D., Dimitrijević, S. I., Ahrenkiel, S. P.,& Nedeljković, J.. (2017). Synthesis, Characterization, and Antimicrobial Activity of Silver Nanoparticles on Poly(GMA-co-EGDMA) Polymer Support. in Polymer Composites, 38(6), 1206-1214.
https://doi.org/10.1002/pc.23684
Vukoje ID, Džunuzović ES, Lončarević D, Dimitrijević SI, Ahrenkiel SP, Nedeljković J. Synthesis, Characterization, and Antimicrobial Activity of Silver Nanoparticles on Poly(GMA-co-EGDMA) Polymer Support. in Polymer Composites. 2017;38(6):1206-1214.
doi:10.1002/pc.23684 .
Vukoje, Ivana D., Džunuzović, Enis S., Lončarević, Davor, Dimitrijević, Suzana I., Ahrenkiel, Scott Phillip, Nedeljković, Jovan, "Synthesis, Characterization, and Antimicrobial Activity of Silver Nanoparticles on Poly(GMA-co-EGDMA) Polymer Support" in Polymer Composites, 38, no. 6 (2017):1206-1214,
https://doi.org/10.1002/pc.23684 . .
15
12
14

Antimicrobial and Photocatalytic Abilities of Ag2CO3 Nano-Rods

Lončarević, Davor; Vukoje, Ivana D.; Dostanic, Jasmina; Bjelajac, Anđelika; Đorđević, Vesna R.; Dimitrijević, Suzana I.; Nedeljković, Jovan

(2017)

TY  - JOUR
AU  - Lončarević, Davor
AU  - Vukoje, Ivana D.
AU  - Dostanic, Jasmina
AU  - Bjelajac, Anđelika
AU  - Đorđević, Vesna R.
AU  - Dimitrijević, Suzana I.
AU  - Nedeljković, Jovan
PY  - 2017
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1499
AB  - The rod-like Ag2CO3 particles (2-4 3 0.3-0.6 mm, length 3 diameter) were synthesized in water by the precipitation reaction between AgNO3 and NaHCO3 in the presence of polyvinylpyrrolidone. The X-ray diffraction analysis revealed the co-existence of monoclinic and hexagonal phases of Ag2CO3, without presence of impurities. The band gap energy of Ag-2 CO3 was found to be 1.4 eV from the diffuse reflectance spectra. Photocatalytic ability of Ag2CO3 was tested using degradation reaction of the organic dye methylene blue over the wide range of concentrations, as well as under long run working conditions in repeated cycles. The photocatalytic mechanism was discussed in terms of the relative energetics of valence and conduction band. Antimicrobial efficiency of Ag-2 CO3 in dark was tested against Gram-negative bacteria E. coli. The Ag2CO3 dispersions in the concentration range 0.1-1.0 mg/mL ensured 100% reduction of bacteria cells. Time-dependent measurements revealed that reduction rates of bacteria cells vary in ascending order with the content of Ag2CO3. On the other hand, the observed reduction rates of bacteria cells do not depend on the concentration of coexisting free Ag+ ions (from 2 to 25 mg/L) present in Ag2CO3 dispersion.
T2  - Chemistryselect
T1  - Antimicrobial and Photocatalytic Abilities of Ag2CO3 Nano-Rods
VL  - 2
IS  - 10
SP  - 2931
EP  - 2938
DO  - 10.1002/slct.201700003
ER  - 
@article{
author = "Lončarević, Davor and Vukoje, Ivana D. and Dostanic, Jasmina and Bjelajac, Anđelika and Đorđević, Vesna R. and Dimitrijević, Suzana I. and Nedeljković, Jovan",
year = "2017",
abstract = "The rod-like Ag2CO3 particles (2-4 3 0.3-0.6 mm, length 3 diameter) were synthesized in water by the precipitation reaction between AgNO3 and NaHCO3 in the presence of polyvinylpyrrolidone. The X-ray diffraction analysis revealed the co-existence of monoclinic and hexagonal phases of Ag2CO3, without presence of impurities. The band gap energy of Ag-2 CO3 was found to be 1.4 eV from the diffuse reflectance spectra. Photocatalytic ability of Ag2CO3 was tested using degradation reaction of the organic dye methylene blue over the wide range of concentrations, as well as under long run working conditions in repeated cycles. The photocatalytic mechanism was discussed in terms of the relative energetics of valence and conduction band. Antimicrobial efficiency of Ag-2 CO3 in dark was tested against Gram-negative bacteria E. coli. The Ag2CO3 dispersions in the concentration range 0.1-1.0 mg/mL ensured 100% reduction of bacteria cells. Time-dependent measurements revealed that reduction rates of bacteria cells vary in ascending order with the content of Ag2CO3. On the other hand, the observed reduction rates of bacteria cells do not depend on the concentration of coexisting free Ag+ ions (from 2 to 25 mg/L) present in Ag2CO3 dispersion.",
journal = "Chemistryselect",
title = "Antimicrobial and Photocatalytic Abilities of Ag2CO3 Nano-Rods",
volume = "2",
number = "10",
pages = "2931-2938",
doi = "10.1002/slct.201700003"
}
Lončarević, D., Vukoje, I. D., Dostanic, J., Bjelajac, A., Đorđević, V. R., Dimitrijević, S. I.,& Nedeljković, J.. (2017). Antimicrobial and Photocatalytic Abilities of Ag2CO3 Nano-Rods. in Chemistryselect, 2(10), 2931-2938.
https://doi.org/10.1002/slct.201700003
Lončarević D, Vukoje ID, Dostanic J, Bjelajac A, Đorđević VR, Dimitrijević SI, Nedeljković J. Antimicrobial and Photocatalytic Abilities of Ag2CO3 Nano-Rods. in Chemistryselect. 2017;2(10):2931-2938.
doi:10.1002/slct.201700003 .
Lončarević, Davor, Vukoje, Ivana D., Dostanic, Jasmina, Bjelajac, Anđelika, Đorđević, Vesna R., Dimitrijević, Suzana I., Nedeljković, Jovan, "Antimicrobial and Photocatalytic Abilities of Ag2CO3 Nano-Rods" in Chemistryselect, 2, no. 10 (2017):2931-2938,
https://doi.org/10.1002/slct.201700003 . .
8
7
8

Density functional theory modeling of C-Au chemical bond formation in gold implanted polyethylene

Antusek, Andrej; Blasko, Martin; Urban, Miroslav; Noga, Pavol; Kisić, Danilo; Nenadović, Miloš; Lončarević, Davor; Rakočević, Zlatko Lj.

(2017)

TY  - JOUR
AU  - Antusek, Andrej
AU  - Blasko, Martin
AU  - Urban, Miroslav
AU  - Noga, Pavol
AU  - Kisić, Danilo
AU  - Nenadović, Miloš
AU  - Lončarević, Davor
AU  - Rakočević, Zlatko Lj.
PY  - 2017
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1809
AB  - We have studied processes of gold ion implantation in polyethylene (PE) by theoretical chemistry methods. Car-Parrinello molecular dynamics (CPMD) simulations of collisions and following chemical kinetics considerations lead to the conclusion that chemical bonds between gold atoms and PE chains are formed. We have identified and characterized by a DFT method various stable structures with C-Au, C-Au-C, C-Au-H and C-Au center dot center dot center dot H-2 types of chemical bonds. The binding energies (BE) of C-Au bonds are as high as 227 kJ mol(-1) and the bond analysis reveals a covalent bonding character. For the experimental detection of these structures in gold implanted PE, we predicted characteristic infra-red (IR) frequencies. The C-Au stretching vibrational modes lie around 500 cm(-1). Other characteristic frequencies lie in a band between 730 cm(-1) and 1500 cm(-1).
T2  - Physical Chemistry Chemical Physics
T1  - Density functional theory modeling of C-Au chemical bond formation in gold implanted polyethylene
VL  - 19
IS  - 42
SP  - 28897
EP  - 28906
DO  - 10.1039/c7cp05637k
ER  - 
@article{
author = "Antusek, Andrej and Blasko, Martin and Urban, Miroslav and Noga, Pavol and Kisić, Danilo and Nenadović, Miloš and Lončarević, Davor and Rakočević, Zlatko Lj.",
year = "2017",
abstract = "We have studied processes of gold ion implantation in polyethylene (PE) by theoretical chemistry methods. Car-Parrinello molecular dynamics (CPMD) simulations of collisions and following chemical kinetics considerations lead to the conclusion that chemical bonds between gold atoms and PE chains are formed. We have identified and characterized by a DFT method various stable structures with C-Au, C-Au-C, C-Au-H and C-Au center dot center dot center dot H-2 types of chemical bonds. The binding energies (BE) of C-Au bonds are as high as 227 kJ mol(-1) and the bond analysis reveals a covalent bonding character. For the experimental detection of these structures in gold implanted PE, we predicted characteristic infra-red (IR) frequencies. The C-Au stretching vibrational modes lie around 500 cm(-1). Other characteristic frequencies lie in a band between 730 cm(-1) and 1500 cm(-1).",
journal = "Physical Chemistry Chemical Physics",
title = "Density functional theory modeling of C-Au chemical bond formation in gold implanted polyethylene",
volume = "19",
number = "42",
pages = "28897-28906",
doi = "10.1039/c7cp05637k"
}
Antusek, A., Blasko, M., Urban, M., Noga, P., Kisić, D., Nenadović, M., Lončarević, D.,& Rakočević, Z. Lj.. (2017). Density functional theory modeling of C-Au chemical bond formation in gold implanted polyethylene. in Physical Chemistry Chemical Physics, 19(42), 28897-28906.
https://doi.org/10.1039/c7cp05637k
Antusek A, Blasko M, Urban M, Noga P, Kisić D, Nenadović M, Lončarević D, Rakočević ZL. Density functional theory modeling of C-Au chemical bond formation in gold implanted polyethylene. in Physical Chemistry Chemical Physics. 2017;19(42):28897-28906.
doi:10.1039/c7cp05637k .
Antusek, Andrej, Blasko, Martin, Urban, Miroslav, Noga, Pavol, Kisić, Danilo, Nenadović, Miloš, Lončarević, Davor, Rakočević, Zlatko Lj., "Density functional theory modeling of C-Au chemical bond formation in gold implanted polyethylene" in Physical Chemistry Chemical Physics, 19, no. 42 (2017):28897-28906,
https://doi.org/10.1039/c7cp05637k . .
7
7

The photocatalytic performance of silver halides - Silver carbonate heterostructures

Dostanic, Jasmina; Lončarević, Davor; Đorđević, Vesna R.; Ahrenkiel, Scott Phillip; Nedeljković, Jovan

(2017)

TY  - JOUR
AU  - Dostanic, Jasmina
AU  - Lončarević, Davor
AU  - Đorđević, Vesna R.
AU  - Ahrenkiel, Scott Phillip
AU  - Nedeljković, Jovan
PY  - 2017
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1425
AB  - The synthesized rod-like Ag2CO3 particles (2-4 x 0.3-0.6 mu m, length x diameter) served as a precursor for preparation of the AgX/Ag2CO3 (X = CI, I) composites by ion exchange method. The various microstructural (X-ray diffraction analysis, transmission electron microscopy, nitrogen adsorption desorption isotherms) and optical (diffuse reflection spectroscopy) techniques were used for thorough characterization of obtained heterostructures. The enhanced photocatalytic performance of AgX/Ag2CO3 heterostructures in comparison to Ag2CO3 nanorods (NRs) was evidenced using degradation of organic dye methylene blue as a test reaction. Also, the formation of composites improved their stability under long run illumination conditions. The effect of AgX content on photocatalytic activity of the composites were also investigated. The possible photocatalytic mechanism that facilitates efficient separation of photo-formed charge carriers in heterostructures was discussed in terms of the relative energetic of valence and conduction bands. (C) 2016 Elsevier B.V. All rights reserved.
T2  - Journal of Photochemistry and Photobiology. A: Chemistry
T1  - The photocatalytic performance of silver halides - Silver carbonate heterostructures
VL  - 336
SP  - 1
EP  - 7
DO  - 10.1016/j.jphotochem.2016.12.019
ER  - 
@article{
author = "Dostanic, Jasmina and Lončarević, Davor and Đorđević, Vesna R. and Ahrenkiel, Scott Phillip and Nedeljković, Jovan",
year = "2017",
abstract = "The synthesized rod-like Ag2CO3 particles (2-4 x 0.3-0.6 mu m, length x diameter) served as a precursor for preparation of the AgX/Ag2CO3 (X = CI, I) composites by ion exchange method. The various microstructural (X-ray diffraction analysis, transmission electron microscopy, nitrogen adsorption desorption isotherms) and optical (diffuse reflection spectroscopy) techniques were used for thorough characterization of obtained heterostructures. The enhanced photocatalytic performance of AgX/Ag2CO3 heterostructures in comparison to Ag2CO3 nanorods (NRs) was evidenced using degradation of organic dye methylene blue as a test reaction. Also, the formation of composites improved their stability under long run illumination conditions. The effect of AgX content on photocatalytic activity of the composites were also investigated. The possible photocatalytic mechanism that facilitates efficient separation of photo-formed charge carriers in heterostructures was discussed in terms of the relative energetic of valence and conduction bands. (C) 2016 Elsevier B.V. All rights reserved.",
journal = "Journal of Photochemistry and Photobiology. A: Chemistry",
title = "The photocatalytic performance of silver halides - Silver carbonate heterostructures",
volume = "336",
pages = "1-7",
doi = "10.1016/j.jphotochem.2016.12.019"
}
Dostanic, J., Lončarević, D., Đorđević, V. R., Ahrenkiel, S. P.,& Nedeljković, J.. (2017). The photocatalytic performance of silver halides - Silver carbonate heterostructures. in Journal of Photochemistry and Photobiology. A: Chemistry, 336, 1-7.
https://doi.org/10.1016/j.jphotochem.2016.12.019
Dostanic J, Lončarević D, Đorđević VR, Ahrenkiel SP, Nedeljković J. The photocatalytic performance of silver halides - Silver carbonate heterostructures. in Journal of Photochemistry and Photobiology. A: Chemistry. 2017;336:1-7.
doi:10.1016/j.jphotochem.2016.12.019 .
Dostanic, Jasmina, Lončarević, Davor, Đorđević, Vesna R., Ahrenkiel, Scott Phillip, Nedeljković, Jovan, "The photocatalytic performance of silver halides - Silver carbonate heterostructures" in Journal of Photochemistry and Photobiology. A: Chemistry, 336 (2017):1-7,
https://doi.org/10.1016/j.jphotochem.2016.12.019 . .
5
5
5
5

Photocatalytic Ability of Visible-Light-Responsive TiO2 Nanoparticles

Vukoje, Ivana D.; Kovač, Tijana S.; Džunuzović, Jasna V.; Džunuzović, Enis S.; Lončarević, Davor; Ahrenkiel, Scott Phillip; Nedeljković, Jovan

(2016)

TY  - JOUR
AU  - Vukoje, Ivana D.
AU  - Kovač, Tijana S.
AU  - Džunuzović, Jasna V.
AU  - Džunuzović, Enis S.
AU  - Lončarević, Davor
AU  - Ahrenkiel, Scott Phillip
AU  - Nedeljković, Jovan
PY  - 2016
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1221
AB  - The synthetic procedures for preparation of free-standing and attached to polymer support surface modified TiO2 nanoparticles (NPs) with absorption extended into the visible spectral region due to charge transfer complex formation were developed. The one-step synthesis of colloids consisting of surface-modified TiO2 NPs is based on the reaction between titanium(IV) isopropoxide (TTIP) and lauryl galatte in nonprotic organic solvents (tetrahydrofuran, xylol, chloroform). The poly(GMA-co-EGDMA) copolymer decorated with surface-modified TiO2 NPs was obtained in two steps. First, copolymer was functionalized with dopamine and then treated with TTIP in organic solvent at slightly elevated temperature. Thorough microstructural and optical characterization of free-standing and attached to polymer support surface-modified TiO2 NPs was performed involving transmission electron microscopy as well as absorption and reflection spectroscopy. Infrared spectroscopy was used to understand coordination of ligands to surface Ti atoms. Photoredox chemistry of surface-modified TiO2 NPs attached to the polymer support was tested. Enhanced photooxidative ability of composite was demonstrated by degradation of organic dye crystal violet under visible light illumination, i.e., using photons with energy smaller than 2.75 eV. On the other hand, photocatalytic hydrogen production was used to demonstrate photoreduction ability of surface modified TiO2 NPs attached to the polymer support.
T2  - Journal of Physical Chemistry. C
T1  - Photocatalytic Ability of Visible-Light-Responsive TiO2 Nanoparticles
VL  - 120
IS  - 33
SP  - 18560
EP  - 18569
DO  - 10.1021/acs.jpcc.6b04293
ER  - 
@article{
author = "Vukoje, Ivana D. and Kovač, Tijana S. and Džunuzović, Jasna V. and Džunuzović, Enis S. and Lončarević, Davor and Ahrenkiel, Scott Phillip and Nedeljković, Jovan",
year = "2016",
abstract = "The synthetic procedures for preparation of free-standing and attached to polymer support surface modified TiO2 nanoparticles (NPs) with absorption extended into the visible spectral region due to charge transfer complex formation were developed. The one-step synthesis of colloids consisting of surface-modified TiO2 NPs is based on the reaction between titanium(IV) isopropoxide (TTIP) and lauryl galatte in nonprotic organic solvents (tetrahydrofuran, xylol, chloroform). The poly(GMA-co-EGDMA) copolymer decorated with surface-modified TiO2 NPs was obtained in two steps. First, copolymer was functionalized with dopamine and then treated with TTIP in organic solvent at slightly elevated temperature. Thorough microstructural and optical characterization of free-standing and attached to polymer support surface-modified TiO2 NPs was performed involving transmission electron microscopy as well as absorption and reflection spectroscopy. Infrared spectroscopy was used to understand coordination of ligands to surface Ti atoms. Photoredox chemistry of surface-modified TiO2 NPs attached to the polymer support was tested. Enhanced photooxidative ability of composite was demonstrated by degradation of organic dye crystal violet under visible light illumination, i.e., using photons with energy smaller than 2.75 eV. On the other hand, photocatalytic hydrogen production was used to demonstrate photoreduction ability of surface modified TiO2 NPs attached to the polymer support.",
journal = "Journal of Physical Chemistry. C",
title = "Photocatalytic Ability of Visible-Light-Responsive TiO2 Nanoparticles",
volume = "120",
number = "33",
pages = "18560-18569",
doi = "10.1021/acs.jpcc.6b04293"
}
Vukoje, I. D., Kovač, T. S., Džunuzović, J. V., Džunuzović, E. S., Lončarević, D., Ahrenkiel, S. P.,& Nedeljković, J.. (2016). Photocatalytic Ability of Visible-Light-Responsive TiO2 Nanoparticles. in Journal of Physical Chemistry. C, 120(33), 18560-18569.
https://doi.org/10.1021/acs.jpcc.6b04293
Vukoje ID, Kovač TS, Džunuzović JV, Džunuzović ES, Lončarević D, Ahrenkiel SP, Nedeljković J. Photocatalytic Ability of Visible-Light-Responsive TiO2 Nanoparticles. in Journal of Physical Chemistry. C. 2016;120(33):18560-18569.
doi:10.1021/acs.jpcc.6b04293 .
Vukoje, Ivana D., Kovač, Tijana S., Džunuzović, Jasna V., Džunuzović, Enis S., Lončarević, Davor, Ahrenkiel, Scott Phillip, Nedeljković, Jovan, "Photocatalytic Ability of Visible-Light-Responsive TiO2 Nanoparticles" in Journal of Physical Chemistry. C, 120, no. 33 (2016):18560-18569,
https://doi.org/10.1021/acs.jpcc.6b04293 . .
28
27
27

Simultaneous photodegradation of two textile dyes using TiO2 as a catalyst

Lončarević, Davor; Dostanić, Jasmina; Radonjić, Vojkan D.; Živković, Ljiljana; Jovanović, Dušan M.

(Springer, 2016)

TY  - JOUR
AU  - Lončarević, Davor
AU  - Dostanić, Jasmina
AU  - Radonjić, Vojkan D.
AU  - Živković, Ljiljana
AU  - Jovanović, Dušan M.
PY  - 2016
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1079
AB  - The simultaneous photocatalytic degradation of two dyes: methylene blue (MB), a cationic dye, and arylazo pyridone dye (SD), an anionic dye was investigated using sol-gel prepared TiO2 particles. The paper shows the main difference in degradation kinetics between single dye solution and binary dye solutions. The effects of competitive adsorption and the concentration of the dyes on degradation rate were analyzed. The preferential adsorption capacity of TiO2 toward MB was attributed to electrostatic interactions between the cationic dye and negatively charged TiO2 surface, while repulsion between the negatively charged surface of the catalyst and SD dye results in its lower adsorption capacity. The TiO2 surface charge and accordingly adsorption affinity of investigated dyes were found to be the main factors affecting degradation rate of the dyes. In the single dye system, the catalyst showed considerably higher degradation activity toward MB than to SD. In binary dye systems, the presence of SD did not affect the degradation of MB. On the other hand, the degradation efficiency of SD was found to be highly influenced by initial MB concentration and absorption ability of MB. In addition, higher MB concentration induces the production of a higher amount of reaction products, which also determine the SD degradation rate. Three kinetic regimes for the photodegradation of SD in binary mixtures were observed, used as a starting point to elucidate most influencing parameters for SD reaction kinetics.
PB  - Springer
T2  - Reaction Kinetics, Mechanisms and Catalysis
T1  - Simultaneous photodegradation of two textile dyes using TiO2 as a catalyst
VL  - 118
IS  - 1
SP  - 153
EP  - 164
DO  - 10.1007/s11144-016-0990-0
ER  - 
@article{
author = "Lončarević, Davor and Dostanić, Jasmina and Radonjić, Vojkan D. and Živković, Ljiljana and Jovanović, Dušan M.",
year = "2016",
abstract = "The simultaneous photocatalytic degradation of two dyes: methylene blue (MB), a cationic dye, and arylazo pyridone dye (SD), an anionic dye was investigated using sol-gel prepared TiO2 particles. The paper shows the main difference in degradation kinetics between single dye solution and binary dye solutions. The effects of competitive adsorption and the concentration of the dyes on degradation rate were analyzed. The preferential adsorption capacity of TiO2 toward MB was attributed to electrostatic interactions between the cationic dye and negatively charged TiO2 surface, while repulsion between the negatively charged surface of the catalyst and SD dye results in its lower adsorption capacity. The TiO2 surface charge and accordingly adsorption affinity of investigated dyes were found to be the main factors affecting degradation rate of the dyes. In the single dye system, the catalyst showed considerably higher degradation activity toward MB than to SD. In binary dye systems, the presence of SD did not affect the degradation of MB. On the other hand, the degradation efficiency of SD was found to be highly influenced by initial MB concentration and absorption ability of MB. In addition, higher MB concentration induces the production of a higher amount of reaction products, which also determine the SD degradation rate. Three kinetic regimes for the photodegradation of SD in binary mixtures were observed, used as a starting point to elucidate most influencing parameters for SD reaction kinetics.",
publisher = "Springer",
journal = "Reaction Kinetics, Mechanisms and Catalysis",
title = "Simultaneous photodegradation of two textile dyes using TiO2 as a catalyst",
volume = "118",
number = "1",
pages = "153-164",
doi = "10.1007/s11144-016-0990-0"
}
Lončarević, D., Dostanić, J., Radonjić, V. D., Živković, L.,& Jovanović, D. M.. (2016). Simultaneous photodegradation of two textile dyes using TiO2 as a catalyst. in Reaction Kinetics, Mechanisms and Catalysis
Springer., 118(1), 153-164.
https://doi.org/10.1007/s11144-016-0990-0
Lončarević D, Dostanić J, Radonjić VD, Živković L, Jovanović DM. Simultaneous photodegradation of two textile dyes using TiO2 as a catalyst. in Reaction Kinetics, Mechanisms and Catalysis. 2016;118(1):153-164.
doi:10.1007/s11144-016-0990-0 .
Lončarević, Davor, Dostanić, Jasmina, Radonjić, Vojkan D., Živković, Ljiljana, Jovanović, Dušan M., "Simultaneous photodegradation of two textile dyes using TiO2 as a catalyst" in Reaction Kinetics, Mechanisms and Catalysis, 118, no. 1 (2016):153-164,
https://doi.org/10.1007/s11144-016-0990-0 . .
17
14
15

Visible light absorption of surface modified TiO2 powders with bidentate benzene derivatives

Milićević, Bojana R.; Đorđević, Vesna R.; Lončarević, Davor; Ahrenkiel, Scott Phillip; Dramićanin, Miroslav; Nedeljković, Jovan

(2015)

TY  - JOUR
AU  - Milićević, Bojana R.
AU  - Đorđević, Vesna R.
AU  - Lončarević, Davor
AU  - Ahrenkiel, Scott Phillip
AU  - Dramićanin, Miroslav
AU  - Nedeljković, Jovan
PY  - 2015
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/719
AB  - TiO2 powders with different specific surface area were prepared using reproducible, sol gel synthetic route and their ability to form hybrids with catechol and 5-amino salicylic acid was compared with the commercially available Degussa P25 TiO2 powder. Microstructural characterization involving transmission electron microscopy, X-ray diffraction analysis and nitrogen adsorption-desorption isotherms indicated that TiO2 samples cover reasonably wide size and/or specific surface area range (50-115 m(2)/g). The surface modification of TiO2 powders with catechol and 5-amino salicylic acid induced significant shift of absorption to the visible spectral region due to charge transfer complex formation. It should be emphasized that tunable optical properties of TiO2 in powder form have never been reported in the literature. The largest red shift of the absorption onset was observed for sample with the largest specific surface area upon surface modification with both ligands. The binding of the modifier molecules to the surface Ti atoms was studied using Fourier transform infrared spectroscopy. (C) 2015 Elsevier Inc. All rights reserved.
T2  - Microporous and Mesoporous Materials
T1  - Visible light absorption of surface modified TiO2 powders with bidentate benzene derivatives
VL  - 217
SP  - 184
EP  - 189
DO  - 10.1016/j.micromeso.2015.06.028
ER  - 
@article{
author = "Milićević, Bojana R. and Đorđević, Vesna R. and Lončarević, Davor and Ahrenkiel, Scott Phillip and Dramićanin, Miroslav and Nedeljković, Jovan",
year = "2015",
abstract = "TiO2 powders with different specific surface area were prepared using reproducible, sol gel synthetic route and their ability to form hybrids with catechol and 5-amino salicylic acid was compared with the commercially available Degussa P25 TiO2 powder. Microstructural characterization involving transmission electron microscopy, X-ray diffraction analysis and nitrogen adsorption-desorption isotherms indicated that TiO2 samples cover reasonably wide size and/or specific surface area range (50-115 m(2)/g). The surface modification of TiO2 powders with catechol and 5-amino salicylic acid induced significant shift of absorption to the visible spectral region due to charge transfer complex formation. It should be emphasized that tunable optical properties of TiO2 in powder form have never been reported in the literature. The largest red shift of the absorption onset was observed for sample with the largest specific surface area upon surface modification with both ligands. The binding of the modifier molecules to the surface Ti atoms was studied using Fourier transform infrared spectroscopy. (C) 2015 Elsevier Inc. All rights reserved.",
journal = "Microporous and Mesoporous Materials",
title = "Visible light absorption of surface modified TiO2 powders with bidentate benzene derivatives",
volume = "217",
pages = "184-189",
doi = "10.1016/j.micromeso.2015.06.028"
}
Milićević, B. R., Đorđević, V. R., Lončarević, D., Ahrenkiel, S. P., Dramićanin, M.,& Nedeljković, J.. (2015). Visible light absorption of surface modified TiO2 powders with bidentate benzene derivatives. in Microporous and Mesoporous Materials, 217, 184-189.
https://doi.org/10.1016/j.micromeso.2015.06.028
Milićević BR, Đorđević VR, Lončarević D, Ahrenkiel SP, Dramićanin M, Nedeljković J. Visible light absorption of surface modified TiO2 powders with bidentate benzene derivatives. in Microporous and Mesoporous Materials. 2015;217:184-189.
doi:10.1016/j.micromeso.2015.06.028 .
Milićević, Bojana R., Đorđević, Vesna R., Lončarević, Davor, Ahrenkiel, Scott Phillip, Dramićanin, Miroslav, Nedeljković, Jovan, "Visible light absorption of surface modified TiO2 powders with bidentate benzene derivatives" in Microporous and Mesoporous Materials, 217 (2015):184-189,
https://doi.org/10.1016/j.micromeso.2015.06.028 . .
3
31
29
30

Modification of dense TiO2 particles using polyethylene glycol template: Synthesis, characterization, and photocatalytic activity

Dostanić, Jasmina; Lončarević, Davor; Radosavljević-Mihajlović, Ana S.; Jovanović, Dušan M.

(Springer Nature, 2015)

TY  - JOUR
AU  - Dostanić, Jasmina
AU  - Lončarević, Davor
AU  - Radosavljević-Mihajlović, Ana S.
AU  - Jovanović, Dušan M.
PY  - 2015
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/814
AB  - In this study, an effort has been made to prepare TiO2 materials by sol-gel technique using polyethylene glycol (PEG) as pore directing agent. Different PEG amounts were used during samples preparation in order to investigate the change in intrinsic material properties. The photocatalytic activity of prepared catalysts was estimated by measuring the decomposition of arylazo pyridone dye. The optimum template amount was determined, resulting in catalyst with enhanced textural properties, optimal anatase/rutile ratio and hence improved photocatalytic properties. Specific surface area and anatase/rutile ratio were found to be the main contributing factors to the catalyst activity. A synergistic effect between anatase and rutile TiO2 has been observed, since the presence of relatively inactive rutile phase enhanced the photoactivity of mixed TiO2.
PB  - Springer Nature
T2  - Russian Journal of Physical Chemistry A
T1  - Modification of dense TiO2 particles using polyethylene glycol template: Synthesis, characterization, and photocatalytic activity
VL  - 89
IS  - 13
SP  - 2492
EP  - 2496
DO  - 10.1134/S0036024415130130
ER  - 
@article{
author = "Dostanić, Jasmina and Lončarević, Davor and Radosavljević-Mihajlović, Ana S. and Jovanović, Dušan M.",
year = "2015",
abstract = "In this study, an effort has been made to prepare TiO2 materials by sol-gel technique using polyethylene glycol (PEG) as pore directing agent. Different PEG amounts were used during samples preparation in order to investigate the change in intrinsic material properties. The photocatalytic activity of prepared catalysts was estimated by measuring the decomposition of arylazo pyridone dye. The optimum template amount was determined, resulting in catalyst with enhanced textural properties, optimal anatase/rutile ratio and hence improved photocatalytic properties. Specific surface area and anatase/rutile ratio were found to be the main contributing factors to the catalyst activity. A synergistic effect between anatase and rutile TiO2 has been observed, since the presence of relatively inactive rutile phase enhanced the photoactivity of mixed TiO2.",
publisher = "Springer Nature",
journal = "Russian Journal of Physical Chemistry A",
title = "Modification of dense TiO2 particles using polyethylene glycol template: Synthesis, characterization, and photocatalytic activity",
volume = "89",
number = "13",
pages = "2492-2496",
doi = "10.1134/S0036024415130130"
}
Dostanić, J., Lončarević, D., Radosavljević-Mihajlović, A. S.,& Jovanović, D. M.. (2015). Modification of dense TiO2 particles using polyethylene glycol template: Synthesis, characterization, and photocatalytic activity. in Russian Journal of Physical Chemistry A
Springer Nature., 89(13), 2492-2496.
https://doi.org/10.1134/S0036024415130130
Dostanić J, Lončarević D, Radosavljević-Mihajlović AS, Jovanović DM. Modification of dense TiO2 particles using polyethylene glycol template: Synthesis, characterization, and photocatalytic activity. in Russian Journal of Physical Chemistry A. 2015;89(13):2492-2496.
doi:10.1134/S0036024415130130 .
Dostanić, Jasmina, Lončarević, Davor, Radosavljević-Mihajlović, Ana S., Jovanović, Dušan M., "Modification of dense TiO2 particles using polyethylene glycol template: Synthesis, characterization, and photocatalytic activity" in Russian Journal of Physical Chemistry A, 89, no. 13 (2015):2492-2496,
https://doi.org/10.1134/S0036024415130130 . .

Structure-activity relationship of nanosized porous PEG-modified TiO2 powders in degradation of organic pollutants

Lončarević, Davor; Dostanić, Jasmina; Radonjić, Vojkan D.; Radosavljević-Mihajlović, Ana S.; Jovanović, Dušan M.

(2015)

TY  - JOUR
AU  - Lončarević, Davor
AU  - Dostanić, Jasmina
AU  - Radonjić, Vojkan D.
AU  - Radosavljević-Mihajlović, Ana S.
AU  - Jovanović, Dušan M.
PY  - 2015
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/693
AB  - This study aims to gain insights in structure-activity relationship of TiO2 photocatalysts. For this purpose photocatalysts were synthesized via classical sol-gel method using titanium isopropoxide as a precursor and polyethylene glycols (PEGs) of different molecular mass (M-n = 200, 600, 2000, 10,000) as a template agents. Incorporating PEG into TiO2 network enhanced not only catalyst porous structure, but also increased the fraction of anatase phase. The use of low-molecular-weight PEGs resulted in catalysts with increased anatase content and enlarged specific surface area. The catalyst photoactivity was estimated through degradation of organic pollutants: Reactive Black 5, arylazo pyridone dye and phenol. The results revealed that the photoactivity was following the same order independently of target pollutant: TiO2/P600 GT TiO2/P200 GT TiO2/P2000 GT TiO2/P10000 GT TiO2. BET surface area and anatase fraction, rather than pore diameter or pore volume, were found to be predominant catalyst property determining the activity for particular reaction system. The existence of synergistic effect between anatase and rutile phases was confirmed for the most active catalysts TiO2/P200 and TiO2/P600. These catalysts showed similar activity in dye degradation, while TiO2/P200 displayed significantly lower activity in phenol degradation, which was attributed to its lower sorption capacity and lower UV light utilization. The difference in the reactivity between investigated pollutants was discussed in relationship with their size, structure and sorption ability. (C) 2015 The Society of Powder Technology Japan. Published by Elsevier B.V. and The Society of Powder Technology Japan. All rights reserved.
T2  - Advanced Powder Technology
T1  - Structure-activity relationship of nanosized porous PEG-modified TiO2 powders in degradation of organic pollutants
VL  - 26
IS  - 4
SP  - 1162
EP  - 1170
DO  - 10.1016/j.apt.2015.05.012
ER  - 
@article{
author = "Lončarević, Davor and Dostanić, Jasmina and Radonjić, Vojkan D. and Radosavljević-Mihajlović, Ana S. and Jovanović, Dušan M.",
year = "2015",
abstract = "This study aims to gain insights in structure-activity relationship of TiO2 photocatalysts. For this purpose photocatalysts were synthesized via classical sol-gel method using titanium isopropoxide as a precursor and polyethylene glycols (PEGs) of different molecular mass (M-n = 200, 600, 2000, 10,000) as a template agents. Incorporating PEG into TiO2 network enhanced not only catalyst porous structure, but also increased the fraction of anatase phase. The use of low-molecular-weight PEGs resulted in catalysts with increased anatase content and enlarged specific surface area. The catalyst photoactivity was estimated through degradation of organic pollutants: Reactive Black 5, arylazo pyridone dye and phenol. The results revealed that the photoactivity was following the same order independently of target pollutant: TiO2/P600 GT TiO2/P200 GT TiO2/P2000 GT TiO2/P10000 GT TiO2. BET surface area and anatase fraction, rather than pore diameter or pore volume, were found to be predominant catalyst property determining the activity for particular reaction system. The existence of synergistic effect between anatase and rutile phases was confirmed for the most active catalysts TiO2/P200 and TiO2/P600. These catalysts showed similar activity in dye degradation, while TiO2/P200 displayed significantly lower activity in phenol degradation, which was attributed to its lower sorption capacity and lower UV light utilization. The difference in the reactivity between investigated pollutants was discussed in relationship with their size, structure and sorption ability. (C) 2015 The Society of Powder Technology Japan. Published by Elsevier B.V. and The Society of Powder Technology Japan. All rights reserved.",
journal = "Advanced Powder Technology",
title = "Structure-activity relationship of nanosized porous PEG-modified TiO2 powders in degradation of organic pollutants",
volume = "26",
number = "4",
pages = "1162-1170",
doi = "10.1016/j.apt.2015.05.012"
}
Lončarević, D., Dostanić, J., Radonjić, V. D., Radosavljević-Mihajlović, A. S.,& Jovanović, D. M.. (2015). Structure-activity relationship of nanosized porous PEG-modified TiO2 powders in degradation of organic pollutants. in Advanced Powder Technology, 26(4), 1162-1170.
https://doi.org/10.1016/j.apt.2015.05.012
Lončarević D, Dostanić J, Radonjić VD, Radosavljević-Mihajlović AS, Jovanović DM. Structure-activity relationship of nanosized porous PEG-modified TiO2 powders in degradation of organic pollutants. in Advanced Powder Technology. 2015;26(4):1162-1170.
doi:10.1016/j.apt.2015.05.012 .
Lončarević, Davor, Dostanić, Jasmina, Radonjić, Vojkan D., Radosavljević-Mihajlović, Ana S., Jovanović, Dušan M., "Structure-activity relationship of nanosized porous PEG-modified TiO2 powders in degradation of organic pollutants" in Advanced Powder Technology, 26, no. 4 (2015):1162-1170,
https://doi.org/10.1016/j.apt.2015.05.012 . .
6
5
6

Photocatalytic activity of peg-modified catalysts

Lončarević, Davor; Dostanić, Jasmina; Radosavljević-Mihajlović, Ana S.

(Society of Physical Chemists of Serbia, 2014)

TY  - CONF
AU  - Lončarević, Davor
AU  - Dostanić, Jasmina
AU  - Radosavljević-Mihajlović, Ana S.
PY  - 2014
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/9186
AB  - This work is focused on the influence of polyethylene glycol (PEG) on
structural, textural and photocatalytic properties of titanium dioxide (TiO2)
catalyst. Catalysts were synthesized by sol-gel method using PEG with
different molecular weight (600 and 10000) as pore generating agent. The
results showed that PEG enhances not only porous structure but also change
anatase to rutile ratio. The photocatalytic activity of the synthesized catalyst
was measured by decomposition of phenol. The order of catalyst
photoactivity was: TiO2/P600>TiO2/P10000>TiO2.The difference in catalyst
photoactivity is attributed to their surface area and anatase fraction, rather
then pore size.
PB  - Society of Physical Chemists of Serbia
C3  - PHYSICAL CHEMISTRY 2014: 12th International Conference on Fundamental and Applied Aspects of Physical Chemistry
T1  - Photocatalytic activity of peg-modified catalysts
VL  - C-06-P
ER  - 
@conference{
author = "Lončarević, Davor and Dostanić, Jasmina and Radosavljević-Mihajlović, Ana S.",
year = "2014",
abstract = "This work is focused on the influence of polyethylene glycol (PEG) on
structural, textural and photocatalytic properties of titanium dioxide (TiO2)
catalyst. Catalysts were synthesized by sol-gel method using PEG with
different molecular weight (600 and 10000) as pore generating agent. The
results showed that PEG enhances not only porous structure but also change
anatase to rutile ratio. The photocatalytic activity of the synthesized catalyst
was measured by decomposition of phenol. The order of catalyst
photoactivity was: TiO2/P600>TiO2/P10000>TiO2.The difference in catalyst
photoactivity is attributed to their surface area and anatase fraction, rather
then pore size.",
publisher = "Society of Physical Chemists of Serbia",
journal = "PHYSICAL CHEMISTRY 2014: 12th International Conference on Fundamental and Applied Aspects of Physical Chemistry",
title = "Photocatalytic activity of peg-modified catalysts",
volume = "C-06-P"
}
Lončarević, D., Dostanić, J.,& Radosavljević-Mihajlović, A. S.. (2014). Photocatalytic activity of peg-modified catalysts. in PHYSICAL CHEMISTRY 2014: 12th International Conference on Fundamental and Applied Aspects of Physical Chemistry
Society of Physical Chemists of Serbia., C-06-P.
Lončarević D, Dostanić J, Radosavljević-Mihajlović AS. Photocatalytic activity of peg-modified catalysts. in PHYSICAL CHEMISTRY 2014: 12th International Conference on Fundamental and Applied Aspects of Physical Chemistry. 2014;C-06-P..
Lončarević, Davor, Dostanić, Jasmina, Radosavljević-Mihajlović, Ana S., "Photocatalytic activity of peg-modified catalysts" in PHYSICAL CHEMISTRY 2014: 12th International Conference on Fundamental and Applied Aspects of Physical Chemistry, C-06-P (2014).

Modeling of inherent SO2 capture in coal particles during combustion in fluidized bed

Manovic, V; Grubor, Borislav; Lončarević, Davor

(2006)

TY  - JOUR
AU  - Manovic, V
AU  - Grubor, Borislav
AU  - Lončarević, Davor
PY  - 2006
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/2973
AB  - The process of inherent sulfur capture in coal particles during combustion in fluidized bed was modeled. The significance of the process is in fact that a part of sulfur may be retained in ash, decreasing emission of sulfur oxides. The process, which is also known as sulfur self-retention, is influenced by parameters that depend on coal characteristics and combustion conditions. The interest for this process was increased with the introduction of fluidized bed combustion technology because of its favorable temperatures and other conditions. The presented model is based on a model of porous char particles combustion under fluidized bed conditions, and the changing grain size model of sulfation of the CaO grains dispersed throughout the char particle volume. The phenomena of sintering, reduction of the produced CaSO4 with CO and thermal decomposition of the produced CaSO4 were incorporated in the model, allowing for the different reactivities of various forms of calcium. A temperature-dependent relation for the CaO grain radius takes sintering into account. Reductive and thermal decomposition were taken into account by the corresponding reaction rate constants of the Arrhenius type. The reactivity of the calcium forms in coal was considered by different initial radius of the CaO grains. A comprehensive parametric analysis of the model was done. The model was verified by the experimental results for three low-rank Serbian coals. Samples of different particle size (4.0-7.0, 7.0-10.0 and 10.0-13.0 mm) for each coal were combusted under fluidized bed conditions at three temperatures: 750, 800 and 850 degrees C. The maximal values of inherent sulfur capture at 800 degrees C were obtained. The comparison with the experimentally obtained results showed that the model can adequately predict the levels of the obtained values of sulfur self-retention efficiencies, as well as the influence of temperature, coal type and coal particle size. (c) 2005 Elsevier Ltd. All rights reserved.
T2  - Chemical Engineering Science
T1  - Modeling of inherent SO2 capture in coal particles during combustion in fluidized bed
VL  - 61
IS  - 5
SP  - 1676
EP  - 1685
DO  - 10.1016/j.ces.2005.10.003
ER  - 
@article{
author = "Manovic, V and Grubor, Borislav and Lončarević, Davor",
year = "2006",
abstract = "The process of inherent sulfur capture in coal particles during combustion in fluidized bed was modeled. The significance of the process is in fact that a part of sulfur may be retained in ash, decreasing emission of sulfur oxides. The process, which is also known as sulfur self-retention, is influenced by parameters that depend on coal characteristics and combustion conditions. The interest for this process was increased with the introduction of fluidized bed combustion technology because of its favorable temperatures and other conditions. The presented model is based on a model of porous char particles combustion under fluidized bed conditions, and the changing grain size model of sulfation of the CaO grains dispersed throughout the char particle volume. The phenomena of sintering, reduction of the produced CaSO4 with CO and thermal decomposition of the produced CaSO4 were incorporated in the model, allowing for the different reactivities of various forms of calcium. A temperature-dependent relation for the CaO grain radius takes sintering into account. Reductive and thermal decomposition were taken into account by the corresponding reaction rate constants of the Arrhenius type. The reactivity of the calcium forms in coal was considered by different initial radius of the CaO grains. A comprehensive parametric analysis of the model was done. The model was verified by the experimental results for three low-rank Serbian coals. Samples of different particle size (4.0-7.0, 7.0-10.0 and 10.0-13.0 mm) for each coal were combusted under fluidized bed conditions at three temperatures: 750, 800 and 850 degrees C. The maximal values of inherent sulfur capture at 800 degrees C were obtained. The comparison with the experimentally obtained results showed that the model can adequately predict the levels of the obtained values of sulfur self-retention efficiencies, as well as the influence of temperature, coal type and coal particle size. (c) 2005 Elsevier Ltd. All rights reserved.",
journal = "Chemical Engineering Science",
title = "Modeling of inherent SO2 capture in coal particles during combustion in fluidized bed",
volume = "61",
number = "5",
pages = "1676-1685",
doi = "10.1016/j.ces.2005.10.003"
}
Manovic, V., Grubor, B.,& Lončarević, D.. (2006). Modeling of inherent SO2 capture in coal particles during combustion in fluidized bed. in Chemical Engineering Science, 61(5), 1676-1685.
https://doi.org/10.1016/j.ces.2005.10.003
Manovic V, Grubor B, Lončarević D. Modeling of inherent SO2 capture in coal particles during combustion in fluidized bed. in Chemical Engineering Science. 2006;61(5):1676-1685.
doi:10.1016/j.ces.2005.10.003 .
Manovic, V, Grubor, Borislav, Lončarević, Davor, "Modeling of inherent SO2 capture in coal particles during combustion in fluidized bed" in Chemical Engineering Science, 61, no. 5 (2006):1676-1685,
https://doi.org/10.1016/j.ces.2005.10.003 . .
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