Papan, Jelena

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orcid::0000-0002-1743-5997
  • Papan, Jelena (4)
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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; Stoiljković, Milovan; Ahrenkiel, Scott Phillip; Nedeljković, Jovan M.

(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
AU  - Stoiljković, Milovan
AU  - Ahrenkiel, Scott Phillip
AU  - Nedeljković, Jovan M.
PY  - 2020
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/3795
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 and Stoiljković, Milovan and Ahrenkiel, Scott Phillip and Nedeljković, Jovan M.",
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., Stoiljković, M., Ahrenkiel, S. P.,& Nedeljković, J. M.. (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 I, Stoiljković M, Ahrenkiel SP, Nedeljković JM. 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, Stoiljković, Milovan, Ahrenkiel, Scott Phillip, Nedeljković, Jovan M., "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 . .
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1

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

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

(Elsevier, 2019)

TY  - JOUR
AU  - Dostanić, Jasmina
AU  - Lončarević, Davor
AU  - Pavlović, Vladimir B.
AU  - Papan, Jelena
AU  - Nedeljković, Jovan M.
PY  - 2019
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/3272
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.
PB  - Elsevier
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 M.",
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.",
publisher = "Elsevier",
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. M.. (2019). Efficient photocatalytic hydrogen production over titanate/titania nanostructures modified with nickel. in Ceramics International
Elsevier., 45(15), 19447-19455.
https://doi.org/10.1016/j.ceramint.2019.06.200
Dostanić J, Lončarević D, Pavlović VB, Papan J, Nedeljković JM. 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 M., "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 . .
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4
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Efficient photocatalytic hydrogen production over titanate/titania nanostructures modified with nickel

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

(Elsevier, 2019)

TY  - JOUR
AU  - Dostanić, Jasmina
AU  - Lončarević, Davor
AU  - Pavlović, Vladimir B.
AU  - Papan, Jelena
AU  - Nedeljković, Jovan M.
PY  - 2019
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/3273
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.
PB  - Elsevier
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 M.",
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.",
publisher = "Elsevier",
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. M.. (2019). Efficient photocatalytic hydrogen production over titanate/titania nanostructures modified with nickel. in Ceramics International
Elsevier., 45(15), 19447-19455.
https://doi.org/10.1016/j.ceramint.2019.06.200
Dostanić J, Lončarević D, Pavlović VB, Papan J, Nedeljković JM. 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 M., "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 . .
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4
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Electrochemical Treatment of Reactive Blue 52 Using Zirconium, Palladium and Graphite Electrode

Jović, Milica; Manojlović, Dragan; Stanković, Dalibor; Marković, Marijana; Anđelković, Ivan; Papan, Jelena; Roglić, Goran

(Wiley-Blackwell, Hoboken, 2014)

TY  - JOUR
AU  - Jović, Milica
AU  - Manojlović, Dragan
AU  - Stanković, Dalibor
AU  - Marković, Marijana
AU  - Anđelković, Ivan
AU  - Papan, Jelena
AU  - Roglić, Goran
PY  - 2014
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1544
AB  - Electrochemical treatment is a new trend for the purification of textile industry wastewater which containing azo dyes. In this paper the electrochemical treatment was used for decolorization of azo dye Reactive Blue 52. The efficiency of decolorization was compared for different electrochemical systems which were all equipped with Fisher platinum electrode as anode and a different cathode (Zr, Pd, C) in sodium sulfate as supporting electrolyte. In order to find optimal conditions the influence of various voltage and pH values of initial dye solution was studied. Decolorization rate was monitored by spectrophotometer while degradation products were identified by high performance liquid chromatography-diode array detector (HPLC-DAD). Results of HPLC analysis confirmed presence of various degradation products in electrochemical systems, which indicated different mechanism of degradation. This was also confirmed by Ek-t curve. In terms of power consumption the most cost effective system was with the graphite cathode (C/Pt).
PB  - Wiley-Blackwell, Hoboken
T2  - Clean-Soil Air Water
T1  - Electrochemical Treatment of Reactive Blue 52 Using Zirconium, Palladium and Graphite Electrode
VL  - 42
IS  - 6
SP  - 804
EP  - 808
DO  - 10.1002/clen.201300245
ER  - 
@article{
author = "Jović, Milica and Manojlović, Dragan and Stanković, Dalibor and Marković, Marijana and Anđelković, Ivan and Papan, Jelena and Roglić, Goran",
year = "2014",
abstract = "Electrochemical treatment is a new trend for the purification of textile industry wastewater which containing azo dyes. In this paper the electrochemical treatment was used for decolorization of azo dye Reactive Blue 52. The efficiency of decolorization was compared for different electrochemical systems which were all equipped with Fisher platinum electrode as anode and a different cathode (Zr, Pd, C) in sodium sulfate as supporting electrolyte. In order to find optimal conditions the influence of various voltage and pH values of initial dye solution was studied. Decolorization rate was monitored by spectrophotometer while degradation products were identified by high performance liquid chromatography-diode array detector (HPLC-DAD). Results of HPLC analysis confirmed presence of various degradation products in electrochemical systems, which indicated different mechanism of degradation. This was also confirmed by Ek-t curve. In terms of power consumption the most cost effective system was with the graphite cathode (C/Pt).",
publisher = "Wiley-Blackwell, Hoboken",
journal = "Clean-Soil Air Water",
title = "Electrochemical Treatment of Reactive Blue 52 Using Zirconium, Palladium and Graphite Electrode",
volume = "42",
number = "6",
pages = "804-808",
doi = "10.1002/clen.201300245"
}
Jović, M., Manojlović, D., Stanković, D., Marković, M., Anđelković, I., Papan, J.,& Roglić, G.. (2014). Electrochemical Treatment of Reactive Blue 52 Using Zirconium, Palladium and Graphite Electrode. in Clean-Soil Air Water
Wiley-Blackwell, Hoboken., 42(6), 804-808.
https://doi.org/10.1002/clen.201300245
Jović M, Manojlović D, Stanković D, Marković M, Anđelković I, Papan J, Roglić G. Electrochemical Treatment of Reactive Blue 52 Using Zirconium, Palladium and Graphite Electrode. in Clean-Soil Air Water. 2014;42(6):804-808.
doi:10.1002/clen.201300245 .
Jović, Milica, Manojlović, Dragan, Stanković, Dalibor, Marković, Marijana, Anđelković, Ivan, Papan, Jelena, Roglić, Goran, "Electrochemical Treatment of Reactive Blue 52 Using Zirconium, Palladium and Graphite Electrode" in Clean-Soil Air Water, 42, no. 6 (2014):804-808,
https://doi.org/10.1002/clen.201300245 . .
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