Vulić, Predrag J.

Link to this page

Authority KeyName Variants
orcid::0000-0002-4806-4551
  • Vulić, Predrag J. (23)
  • Vulić, Predrag (2)
Projects
Rational design and synthesis of biologically active and coordination compounds and functional materials, relevant for (bio)nanotechnology Application of advanced oxidation processes and nanostructured oxide materials for the removal of pollutants from the environment, development and optimisation of instrumental techniques for efficiency monitoring
Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200168 (University of Belgrade, Faculty of Chemistry) Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200116 (University of Belgrade, Faculty of Agriculture)
Geochemical investigations of sedimentary rocks - fossil fuels and environmental pollutants The DGI(MEC)/FEDER (CTQ2016-75816-C02-02-P) project is acknowledged for financial support. B.B.H. and N.R.F. gratefully acknowledge help from Prof. Katalin Mészáros Szécsényi, University of Novi Sad, Faculty of Sciences, for her support and valuable advices in TG analysis.
Directed synthesis, structure and properties of multifunctional materials info:eu-repo/grantAgreement/MESTD/inst-2020/200026/RS/
Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200026 (University of Belgrade, Institute of Chemistry, Technology and Metallurgy - IChTM) Eksperimentalna i kliničko-farmakološka istraživanja mehanizma dejstva i interakcija lekova u nervnom i kardiovaskularnom sistemu
Diagnostics and Optimization of Plasma Sources Important for Applications Meteorological extremes and climatic change in Serbia
Magmatism and geodynamics of the Balkan Peninsula from Mesozoic to present day: significance for the formation of metallic and non-metallic mineral deposits Petrogenesis and mineral resources of the carpatho-balkanides and their importance in environmental protection
Studying climate change and its influence on environment: impacts, adaptation and mitigation

Author's Bibliography

The influence of the starch coating on the magnetic properties of nanosized cobalt ferrites obtained by different synthetic methods

Šuljagić, Marija; Vulić, Predrag; Jeremić, Dejan; Pavlović, Vladimir B.; Filipović, Suzana; Kilanski, Lukasz; Lewinska, Sabina; Slawska-Waniewska, Anna; Milenković, Milica R.; Nikolić, Aleksandar S.; Anđelković, Ljubica

(Elsevier, 2021)

TY  - JOUR
AU  - Šuljagić, Marija
AU  - Vulić, Predrag
AU  - Jeremić, Dejan
AU  - Pavlović, Vladimir B.
AU  - Filipović, Suzana
AU  - Kilanski, Lukasz
AU  - Lewinska, Sabina
AU  - Slawska-Waniewska, Anna
AU  - Milenković, Milica R.
AU  - Nikolić, Aleksandar S.
AU  - Anđelković, Ljubica
PY  - 2021
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/4271
AB  - To investigate the magnetic behavior of starch-coated cobalt ferrites, well-established synthetic methods, i.e., coprecipitation, mechanochemical, ultrasonically assisted coprecipitation, microemulsion, and microwave-assisted hydrothermal syntheses were chosen for their preparation. The obtained materials had pure single-phase spinel structures. Scanning and transmission electron microscopy analyses revealed that the morphology of the samples is not uniform, and particle aggregation is a dominant process. Fourier transform infrared spectra and thermogravimetric analysis confirmed the presence of starch in all–coated samples. The unusually higher saturation magnetization of starch-coated samples than their as-prepared analogs, obtained by coprecipitation, ultrasonically assisted coprecipitation, and microwave-assisted hydrothermal methods, might be explained by the Ostwald ripening mechanism induced by the coating process. A decrease in magnetization was noticed for the starch-functionalized nanomaterials synthesized by mechanochemical and microemulsion methods, in comparison to their as-prepared analogs, i.e., the size distribution of such nanoparticles is narrow, and the average diameter of the grains is near critical for the Ostwald ripening process.
PB  - Elsevier
T2  - Materials Research Bulletin
T1  - The influence of the starch coating on the magnetic properties of nanosized cobalt ferrites obtained by different synthetic methods
VL  - 134
SP  - 111117
DO  - 10.1016/j.materresbull.2020.111117
ER  - 
@article{
author = "Šuljagić, Marija and Vulić, Predrag and Jeremić, Dejan and Pavlović, Vladimir B. and Filipović, Suzana and Kilanski, Lukasz and Lewinska, Sabina and Slawska-Waniewska, Anna and Milenković, Milica R. and Nikolić, Aleksandar S. and Anđelković, Ljubica",
year = "2021",
abstract = "To investigate the magnetic behavior of starch-coated cobalt ferrites, well-established synthetic methods, i.e., coprecipitation, mechanochemical, ultrasonically assisted coprecipitation, microemulsion, and microwave-assisted hydrothermal syntheses were chosen for their preparation. The obtained materials had pure single-phase spinel structures. Scanning and transmission electron microscopy analyses revealed that the morphology of the samples is not uniform, and particle aggregation is a dominant process. Fourier transform infrared spectra and thermogravimetric analysis confirmed the presence of starch in all–coated samples. The unusually higher saturation magnetization of starch-coated samples than their as-prepared analogs, obtained by coprecipitation, ultrasonically assisted coprecipitation, and microwave-assisted hydrothermal methods, might be explained by the Ostwald ripening mechanism induced by the coating process. A decrease in magnetization was noticed for the starch-functionalized nanomaterials synthesized by mechanochemical and microemulsion methods, in comparison to their as-prepared analogs, i.e., the size distribution of such nanoparticles is narrow, and the average diameter of the grains is near critical for the Ostwald ripening process.",
publisher = "Elsevier",
journal = "Materials Research Bulletin",
title = "The influence of the starch coating on the magnetic properties of nanosized cobalt ferrites obtained by different synthetic methods",
volume = "134",
pages = "111117",
doi = "10.1016/j.materresbull.2020.111117"
}
Šuljagić, M., Vulić, P., Jeremić, D., Pavlović, V. B., Filipović, S., Kilanski, L., Lewinska, S., Slawska-Waniewska, A., Milenković, M. R., Nikolić, A. S.,& Anđelković, L.. (2021). The influence of the starch coating on the magnetic properties of nanosized cobalt ferrites obtained by different synthetic methods. in Materials Research Bulletin
Elsevier., 134, 111117.
https://doi.org/10.1016/j.materresbull.2020.111117
Šuljagić M, Vulić P, Jeremić D, Pavlović VB, Filipović S, Kilanski L, Lewinska S, Slawska-Waniewska A, Milenković MR, Nikolić AS, Anđelković L. The influence of the starch coating on the magnetic properties of nanosized cobalt ferrites obtained by different synthetic methods. in Materials Research Bulletin. 2021;134:111117.
doi:10.1016/j.materresbull.2020.111117 .
Šuljagić, Marija, Vulić, Predrag, Jeremić, Dejan, Pavlović, Vladimir B., Filipović, Suzana, Kilanski, Lukasz, Lewinska, Sabina, Slawska-Waniewska, Anna, Milenković, Milica R., Nikolić, Aleksandar S., Anđelković, Ljubica, "The influence of the starch coating on the magnetic properties of nanosized cobalt ferrites obtained by different synthetic methods" in Materials Research Bulletin, 134 (2021):111117,
https://doi.org/10.1016/j.materresbull.2020.111117 . .
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Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study

Ristić, Predrag; Blagojević, Vladimir A.; Janjić, Goran V.; Rodić, Marko; Vulić, Predrag J.; Donnard, Morgan; Gulea, Mihaela; Chylewska, Agnieszka; Makowski, Mariusz; Todorović, Tamara; Filipović, Nenad R.

(American Chemical Society, 2020)

TY  - JOUR
AU  - Ristić, Predrag
AU  - Blagojević, Vladimir A.
AU  - Janjić, Goran V.
AU  - Rodić, Marko
AU  - Vulić, Predrag J.
AU  - Donnard, Morgan
AU  - Gulea, Mihaela
AU  - Chylewska, Agnieszka
AU  - Makowski, Mariusz
AU  - Todorović, Tamara
AU  - Filipović, Nenad R.
PY  - 2020
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/4042
AB  - Pt(II) and Pd(II) complexes (1 and 2, respectively) with thiomorpholine-4-carbonitrile (TM-CN), an N-substituted thiomorpholine derivative, were synthesized from tetrachlorido precursors in water. Structural analysis has shown that 1 represents the first monomeric metal complex with this ligand type with an axial M-S bond with respect to the TM-CN ring chair conformation, while in 2 a typical equatorial M-S bond position with respect to the ring chair conformation was observed. A detailed DFT investigation revealed that axial conformers are more stable for molecular forms of both metals, while intermolecular interactions in the crystals stabilize the axial conformer for Pt(II) and the equatorial conformer for Pd(II). The magnitude of this stabilization in the case of 2 is large enough to change the most stable axial conformer in the molecular form to the equatorial conformer in the crystal. Further investigation of the strength of individual intermolecular interactions revealed significant differences of some interactions between the two structures. The likely cause of the difference in the crystal structures of experimentally obtained complexes is the fact that 1 and 2 exhibit different dominant interactions: C-H/M and C-H/S are more dominant in 1 and C-H/Cl interactions are more dominant in 2. In addition, DFT calculations have shown that while the axial position of the Pt-S bond with respect to the ring chair conformation results in a significantly shorter C-H/Pt interaction distance than that in the hypothetical equatorial conformer, there is very little difference in C-H/Pd interaction distances in conformers with axial and equatorial positions of Pd-S bond with respect to the ring chair conformation.
PB  - American Chemical Society
T2  - Crystal Growth & Design
T1  - Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study
VL  - 20
IS  - 5
SP  - 3018
EP  - 3033
DO  - 10.1021/acs.cgd.9b01661
ER  - 
@article{
author = "Ristić, Predrag and Blagojević, Vladimir A. and Janjić, Goran V. and Rodić, Marko and Vulić, Predrag J. and Donnard, Morgan and Gulea, Mihaela and Chylewska, Agnieszka and Makowski, Mariusz and Todorović, Tamara and Filipović, Nenad R.",
year = "2020",
abstract = "Pt(II) and Pd(II) complexes (1 and 2, respectively) with thiomorpholine-4-carbonitrile (TM-CN), an N-substituted thiomorpholine derivative, were synthesized from tetrachlorido precursors in water. Structural analysis has shown that 1 represents the first monomeric metal complex with this ligand type with an axial M-S bond with respect to the TM-CN ring chair conformation, while in 2 a typical equatorial M-S bond position with respect to the ring chair conformation was observed. A detailed DFT investigation revealed that axial conformers are more stable for molecular forms of both metals, while intermolecular interactions in the crystals stabilize the axial conformer for Pt(II) and the equatorial conformer for Pd(II). The magnitude of this stabilization in the case of 2 is large enough to change the most stable axial conformer in the molecular form to the equatorial conformer in the crystal. Further investigation of the strength of individual intermolecular interactions revealed significant differences of some interactions between the two structures. The likely cause of the difference in the crystal structures of experimentally obtained complexes is the fact that 1 and 2 exhibit different dominant interactions: C-H/M and C-H/S are more dominant in 1 and C-H/Cl interactions are more dominant in 2. In addition, DFT calculations have shown that while the axial position of the Pt-S bond with respect to the ring chair conformation results in a significantly shorter C-H/Pt interaction distance than that in the hypothetical equatorial conformer, there is very little difference in C-H/Pd interaction distances in conformers with axial and equatorial positions of Pd-S bond with respect to the ring chair conformation.",
publisher = "American Chemical Society",
journal = "Crystal Growth & Design",
title = "Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study",
volume = "20",
number = "5",
pages = "3018-3033",
doi = "10.1021/acs.cgd.9b01661"
}
Ristić, P., Blagojević, V. A., Janjić, G. V., Rodić, M., Vulić, P. J., Donnard, M., Gulea, M., Chylewska, A., Makowski, M., Todorović, T.,& Filipović, N. R.. (2020). Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study. in Crystal Growth & Design
American Chemical Society., 20(5), 3018-3033.
https://doi.org/10.1021/acs.cgd.9b01661
Ristić P, Blagojević VA, Janjić GV, Rodić M, Vulić PJ, Donnard M, Gulea M, Chylewska A, Makowski M, Todorović T, Filipović NR. Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study. in Crystal Growth & Design. 2020;20(5):3018-3033.
doi:10.1021/acs.cgd.9b01661 .
Ristić, Predrag, Blagojević, Vladimir A., Janjić, Goran V., Rodić, Marko, Vulić, Predrag J., Donnard, Morgan, Gulea, Mihaela, Chylewska, Agnieszka, Makowski, Mariusz, Todorović, Tamara, Filipović, Nenad R., "Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study" in Crystal Growth & Design, 20, no. 5 (2020):3018-3033,
https://doi.org/10.1021/acs.cgd.9b01661 . .
1
3
3
3

Supplementary data for the article: Ristić, P.; Blagojević, V.; Janjić, G.; Rodić, M.; Vulić, P.; Donnard, M.; Gulea, M.; Chylewska, A.; Makowski, M.; Todorović, T.; Filipović, N. Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-Carbonitrile: Crystallographic, Thermal, and DFT Study. Crystal Growth & Design 2020, 20 (5), 3018–3033. https://doi.org/10.1021/acs.cgd.9b01661

Ristić, Predrag; Blagojević, Vladimir A.; Janjić, Goran V.; Rodić, Marko; Vulić, Predrag J.; Donnard, Morgan; Gulea, Mihaela; Chylewska, Agnieszka; Makowski, Mariusz; Todorović, Tamara; Filipović, Nenad R.

(American Chemical Society, 2020)

TY  - DATA
AU  - Ristić, Predrag
AU  - Blagojević, Vladimir A.
AU  - Janjić, Goran V.
AU  - Rodić, Marko
AU  - Vulić, Predrag J.
AU  - Donnard, Morgan
AU  - Gulea, Mihaela
AU  - Chylewska, Agnieszka
AU  - Makowski, Mariusz
AU  - Todorović, Tamara
AU  - Filipović, Nenad R.
PY  - 2020
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/4043
PB  - American Chemical Society
T2  - Crystal Growth & Design
T1  - Supplementary data for the article: Ristić, P.; Blagojević, V.; Janjić, G.; Rodić, M.; Vulić, P.; Donnard, M.; Gulea, M.; Chylewska, A.; Makowski, M.; Todorović, T.; Filipović, N. Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-Carbonitrile: Crystallographic, Thermal, and DFT Study. Crystal Growth & Design 2020, 20 (5), 3018–3033. https://doi.org/10.1021/acs.cgd.9b01661
ER  - 
@misc{
author = "Ristić, Predrag and Blagojević, Vladimir A. and Janjić, Goran V. and Rodić, Marko and Vulić, Predrag J. and Donnard, Morgan and Gulea, Mihaela and Chylewska, Agnieszka and Makowski, Mariusz and Todorović, Tamara and Filipović, Nenad R.",
year = "2020",
publisher = "American Chemical Society",
journal = "Crystal Growth & Design",
title = "Supplementary data for the article: Ristić, P.; Blagojević, V.; Janjić, G.; Rodić, M.; Vulić, P.; Donnard, M.; Gulea, M.; Chylewska, A.; Makowski, M.; Todorović, T.; Filipović, N. Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-Carbonitrile: Crystallographic, Thermal, and DFT Study. Crystal Growth & Design 2020, 20 (5), 3018–3033. https://doi.org/10.1021/acs.cgd.9b01661"
}
Ristić, P., Blagojević, V. A., Janjić, G. V., Rodić, M., Vulić, P. J., Donnard, M., Gulea, M., Chylewska, A., Makowski, M., Todorović, T.,& Filipović, N. R.. (2020). Supplementary data for the article: Ristić, P.; Blagojević, V.; Janjić, G.; Rodić, M.; Vulić, P.; Donnard, M.; Gulea, M.; Chylewska, A.; Makowski, M.; Todorović, T.; Filipović, N. Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-Carbonitrile: Crystallographic, Thermal, and DFT Study. Crystal Growth & Design 2020, 20 (5), 3018–3033. https://doi.org/10.1021/acs.cgd.9b01661. in Crystal Growth & Design
American Chemical Society..
Ristić P, Blagojević VA, Janjić GV, Rodić M, Vulić PJ, Donnard M, Gulea M, Chylewska A, Makowski M, Todorović T, Filipović NR. Supplementary data for the article: Ristić, P.; Blagojević, V.; Janjić, G.; Rodić, M.; Vulić, P.; Donnard, M.; Gulea, M.; Chylewska, A.; Makowski, M.; Todorović, T.; Filipović, N. Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-Carbonitrile: Crystallographic, Thermal, and DFT Study. Crystal Growth & Design 2020, 20 (5), 3018–3033. https://doi.org/10.1021/acs.cgd.9b01661. in Crystal Growth & Design. 2020;..
Ristić, Predrag, Blagojević, Vladimir A., Janjić, Goran V., Rodić, Marko, Vulić, Predrag J., Donnard, Morgan, Gulea, Mihaela, Chylewska, Agnieszka, Makowski, Mariusz, Todorović, Tamara, Filipović, Nenad R., "Supplementary data for the article: Ristić, P.; Blagojević, V.; Janjić, G.; Rodić, M.; Vulić, P.; Donnard, M.; Gulea, M.; Chylewska, A.; Makowski, M.; Todorović, T.; Filipović, N. Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-Carbonitrile: Crystallographic, Thermal, and DFT Study. Crystal Growth & Design 2020, 20 (5), 3018–3033. https://doi.org/10.1021/acs.cgd.9b01661" in Crystal Growth & Design (2020).

1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study

Ristić, Predrag; Todorović, Tamara; Blagojević, Vladimir A.; Klisurić, Olivera; Marjanović, Ivana; Holló, Berta Barta; Vulić, Predrag J.; Gulea, Mihaela; Donnard, Morgan; Monge, Miguel; Rodríguez-Castillo, María; López-de-Luzuriaga, José M.; Filipović, Nenad R.

(American Chemical Society, 2020)

TY  - JOUR
AU  - Ristić, Predrag
AU  - Todorović, Tamara
AU  - Blagojević, Vladimir A.
AU  - Klisurić, Olivera
AU  - Marjanović, Ivana
AU  - Holló, Berta Barta
AU  - Vulić, Predrag J.
AU  - Gulea, Mihaela
AU  - Donnard, Morgan
AU  - Monge, Miguel
AU  - Rodríguez-Castillo, María
AU  - López-de-Luzuriaga, José M.
AU  - Filipović, Nenad R.
PY  - 2020
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/4200
AB  - Four silver-based coordination polymers, {[Ag(L)2](BF4)}∞ (1), {[Ag(H2BTC)(L)]·(H3BTC)}∞ (2), {[Ag2(H2BTEC)(L)2]·3.33H2O}∞ (3), and [Ag(H25SSA)(L)]∞ (4), were synthesized using thiomorpholine-4-carbonitrile (L) as the primary ligand and three aromatic polyoxoacids as coligands: trimesic (H3BTC), pyromellitic (H4BTEC), and 5-sulfosalicylic acid (H35SSA). Compounds 1 and 3 are two-dimensional, while 2 and 4 are one-dimensional. L acts as a bis-monodentate ligand, while the Ag(I) ion is three-coordinated in 2 and four-coordinated in all of the other compounds. The tetrahedral coordination of Ag(I) in 3 leads to an almost complete absence of intermolecular interactions with the metal center. All compounds show reasonable photocatalytic activity for photocatalytic degradation of mordant blue 9 dye, with reaction rates in the 0.036–0.056 min–1 range. Changes in the reaction rates can be correlated with the type and coordination of the coligand. Complex 3 exhibits photoluminescence at 77 K, while 4 exhibits photoluminescence at both room temperature and 77 K. Luminescence lifetimes indicate electronic transitions of singlet parentage, where transitions are allowed. A TD-DFT study determined the contributions of individual singlet–singlet electronic excitations to the fluorescence, indicating that metal– intraligand transitions are responsible for luminescence in both complexes.
PB  - American Chemical Society
T2  - Crystal Growth & Design
T2  - Crystal Growth & DesignCrystal Growth & Design
T1  - 1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study
VL  - 20
IS  - 7
SP  - 4461
EP  - 4478
DO  - 10.1021/acs.cgd.0c00287
ER  - 
@article{
author = "Ristić, Predrag and Todorović, Tamara and Blagojević, Vladimir A. and Klisurić, Olivera and Marjanović, Ivana and Holló, Berta Barta and Vulić, Predrag J. and Gulea, Mihaela and Donnard, Morgan and Monge, Miguel and Rodríguez-Castillo, María and López-de-Luzuriaga, José M. and Filipović, Nenad R.",
year = "2020",
abstract = "Four silver-based coordination polymers, {[Ag(L)2](BF4)}∞ (1), {[Ag(H2BTC)(L)]·(H3BTC)}∞ (2), {[Ag2(H2BTEC)(L)2]·3.33H2O}∞ (3), and [Ag(H25SSA)(L)]∞ (4), were synthesized using thiomorpholine-4-carbonitrile (L) as the primary ligand and three aromatic polyoxoacids as coligands: trimesic (H3BTC), pyromellitic (H4BTEC), and 5-sulfosalicylic acid (H35SSA). Compounds 1 and 3 are two-dimensional, while 2 and 4 are one-dimensional. L acts as a bis-monodentate ligand, while the Ag(I) ion is three-coordinated in 2 and four-coordinated in all of the other compounds. The tetrahedral coordination of Ag(I) in 3 leads to an almost complete absence of intermolecular interactions with the metal center. All compounds show reasonable photocatalytic activity for photocatalytic degradation of mordant blue 9 dye, with reaction rates in the 0.036–0.056 min–1 range. Changes in the reaction rates can be correlated with the type and coordination of the coligand. Complex 3 exhibits photoluminescence at 77 K, while 4 exhibits photoluminescence at both room temperature and 77 K. Luminescence lifetimes indicate electronic transitions of singlet parentage, where transitions are allowed. A TD-DFT study determined the contributions of individual singlet–singlet electronic excitations to the fluorescence, indicating that metal– intraligand transitions are responsible for luminescence in both complexes.",
publisher = "American Chemical Society",
journal = "Crystal Growth & Design, Crystal Growth & DesignCrystal Growth & Design",
title = "1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study",
volume = "20",
number = "7",
pages = "4461-4478",
doi = "10.1021/acs.cgd.0c00287"
}
Ristić, P., Todorović, T., Blagojević, V. A., Klisurić, O., Marjanović, I., Holló, B. B., Vulić, P. J., Gulea, M., Donnard, M., Monge, M., Rodríguez-Castillo, M., López-de-Luzuriaga, J. M.,& Filipović, N. R.. (2020). 1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study. in Crystal Growth & Design
American Chemical Society., 20(7), 4461-4478.
https://doi.org/10.1021/acs.cgd.0c00287
Ristić P, Todorović T, Blagojević VA, Klisurić O, Marjanović I, Holló BB, Vulić PJ, Gulea M, Donnard M, Monge M, Rodríguez-Castillo M, López-de-Luzuriaga JM, Filipović NR. 1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study. in Crystal Growth & Design. 2020;20(7):4461-4478.
doi:10.1021/acs.cgd.0c00287 .
Ristić, Predrag, Todorović, Tamara, Blagojević, Vladimir A., Klisurić, Olivera, Marjanović, Ivana, Holló, Berta Barta, Vulić, Predrag J., Gulea, Mihaela, Donnard, Morgan, Monge, Miguel, Rodríguez-Castillo, María, López-de-Luzuriaga, José M., Filipović, Nenad R., "1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study" in Crystal Growth & Design, 20, no. 7 (2020):4461-4478,
https://doi.org/10.1021/acs.cgd.0c00287 . .
4
5
5
5

1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study

Ristić, Predrag; Todorović, Tamara; Blagojević, Vladimir A.; Klisurić, Olivera; Marjanović, Ivana; Holló, Berta Barta; Vulić, Predrag J.; Gulea, Mihaela; Donnard, Morgan; Monge, Miguel; Rodríguez-Castillo, María; López-de-Luzuriaga, José M.; Filipović, Nenad R.

(American Chemical Society, 2020)

TY  - JOUR
AU  - Ristić, Predrag
AU  - Todorović, Tamara
AU  - Blagojević, Vladimir A.
AU  - Klisurić, Olivera
AU  - Marjanović, Ivana
AU  - Holló, Berta Barta
AU  - Vulić, Predrag J.
AU  - Gulea, Mihaela
AU  - Donnard, Morgan
AU  - Monge, Miguel
AU  - Rodríguez-Castillo, María
AU  - López-de-Luzuriaga, José M.
AU  - Filipović, Nenad R.
PY  - 2020
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/4203
AB  - Four silver-based coordination polymers, {[Ag(L)2](BF4)}∞ (1), {[Ag(H2BTC)(L)]·(H3BTC)}∞ (2), {[Ag2(H2BTEC)(L)2]·3.33H2O}∞ (3), and [Ag(H25SSA)(L)]∞ (4), were synthesized using thiomorpholine-4-carbonitrile (L) as the primary ligand and three aromatic polyoxoacids as coligands: trimesic (H3BTC), pyromellitic (H4BTEC), and 5-sulfosalicylic acid (H35SSA). Compounds 1 and 3 are two-dimensional, while 2 and 4 are one-dimensional. L acts as a bis-monodentate ligand, while the Ag(I) ion is three-coordinated in 2 and four-coordinated in all of the other compounds. The tetrahedral coordination of Ag(I) in 3 leads to an almost complete absence of intermolecular interactions with the metal center. All compounds show reasonable photocatalytic activity for photocatalytic degradation of mordant blue 9 dye, with reaction rates in the 0.036–0.056 min–1 range. Changes in the reaction rates can be correlated with the type and coordination of the coligand. Complex 3 exhibits photoluminescence at 77 K, while 4 exhibits photoluminescence at both room temperature and 77 K. Luminescence lifetimes indicate electronic transitions of singlet parentage, where transitions are allowed. A TD-DFT study determined the contributions of individual singlet–singlet electronic excitations to the fluorescence, indicating that metal– intraligand transitions are responsible for luminescence in both complexes.
PB  - American Chemical Society
T2  - Crystal Growth & Design
T2  - Crystal Growth & DesignCrystal Growth & Design
T1  - 1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study
VL  - 20
IS  - 7
SP  - 4461
EP  - 4478
DO  - 10.1021/acs.cgd.0c00287
ER  - 
@article{
author = "Ristić, Predrag and Todorović, Tamara and Blagojević, Vladimir A. and Klisurić, Olivera and Marjanović, Ivana and Holló, Berta Barta and Vulić, Predrag J. and Gulea, Mihaela and Donnard, Morgan and Monge, Miguel and Rodríguez-Castillo, María and López-de-Luzuriaga, José M. and Filipović, Nenad R.",
year = "2020",
abstract = "Four silver-based coordination polymers, {[Ag(L)2](BF4)}∞ (1), {[Ag(H2BTC)(L)]·(H3BTC)}∞ (2), {[Ag2(H2BTEC)(L)2]·3.33H2O}∞ (3), and [Ag(H25SSA)(L)]∞ (4), were synthesized using thiomorpholine-4-carbonitrile (L) as the primary ligand and three aromatic polyoxoacids as coligands: trimesic (H3BTC), pyromellitic (H4BTEC), and 5-sulfosalicylic acid (H35SSA). Compounds 1 and 3 are two-dimensional, while 2 and 4 are one-dimensional. L acts as a bis-monodentate ligand, while the Ag(I) ion is three-coordinated in 2 and four-coordinated in all of the other compounds. The tetrahedral coordination of Ag(I) in 3 leads to an almost complete absence of intermolecular interactions with the metal center. All compounds show reasonable photocatalytic activity for photocatalytic degradation of mordant blue 9 dye, with reaction rates in the 0.036–0.056 min–1 range. Changes in the reaction rates can be correlated with the type and coordination of the coligand. Complex 3 exhibits photoluminescence at 77 K, while 4 exhibits photoluminescence at both room temperature and 77 K. Luminescence lifetimes indicate electronic transitions of singlet parentage, where transitions are allowed. A TD-DFT study determined the contributions of individual singlet–singlet electronic excitations to the fluorescence, indicating that metal– intraligand transitions are responsible for luminescence in both complexes.",
publisher = "American Chemical Society",
journal = "Crystal Growth & Design, Crystal Growth & DesignCrystal Growth & Design",
title = "1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study",
volume = "20",
number = "7",
pages = "4461-4478",
doi = "10.1021/acs.cgd.0c00287"
}
Ristić, P., Todorović, T., Blagojević, V. A., Klisurić, O., Marjanović, I., Holló, B. B., Vulić, P. J., Gulea, M., Donnard, M., Monge, M., Rodríguez-Castillo, M., López-de-Luzuriaga, J. M.,& Filipović, N. R.. (2020). 1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study. in Crystal Growth & Design
American Chemical Society., 20(7), 4461-4478.
https://doi.org/10.1021/acs.cgd.0c00287
Ristić P, Todorović T, Blagojević VA, Klisurić O, Marjanović I, Holló BB, Vulić PJ, Gulea M, Donnard M, Monge M, Rodríguez-Castillo M, López-de-Luzuriaga JM, Filipović NR. 1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study. in Crystal Growth & Design. 2020;20(7):4461-4478.
doi:10.1021/acs.cgd.0c00287 .
Ristić, Predrag, Todorović, Tamara, Blagojević, Vladimir A., Klisurić, Olivera, Marjanović, Ivana, Holló, Berta Barta, Vulić, Predrag J., Gulea, Mihaela, Donnard, Morgan, Monge, Miguel, Rodríguez-Castillo, María, López-de-Luzuriaga, José M., Filipović, Nenad R., "1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study" in Crystal Growth & Design, 20, no. 7 (2020):4461-4478,
https://doi.org/10.1021/acs.cgd.0c00287 . .
4
5
5
5

Supplementary data for the article: Ristić, P.; Todorović, T. R.; Blagojević, V.; Klisurić, O. R.; Marjanović, I.; Holló, B. B.; Vulić, P.; Gulea, M.; Donnard, M.; Monge, M.; Rodríguez-Castillo, M.; López-de-Luzuriaga, J. M.; Filipović, N. R. 1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-Carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study. Crystal Growth & Design 2020, 20 (7), 4461–4478. https://doi.org/10.1021/acs.cgd.0c00287

Ristić, Predrag; Todorović, Tamara; Blagojević, Vladimir A.; Klisurić, Olivera; Marjanović, Ivana; Holló, Berta Barta; Vulić, Predrag J.; Gulea, Mihaela; Donnard, Morgan; Monge, Miguel; Rodríguez-Castillo, María; López-de-Luzuriaga, José M.; Filipović, Nenad R.

(American Chemical Society, 2020)

TY  - DATA
AU  - Ristić, Predrag
AU  - Todorović, Tamara
AU  - Blagojević, Vladimir A.
AU  - Klisurić, Olivera
AU  - Marjanović, Ivana
AU  - Holló, Berta Barta
AU  - Vulić, Predrag J.
AU  - Gulea, Mihaela
AU  - Donnard, Morgan
AU  - Monge, Miguel
AU  - Rodríguez-Castillo, María
AU  - López-de-Luzuriaga, José M.
AU  - Filipović, Nenad R.
PY  - 2020
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/4206
PB  - American Chemical Society
T2  - Crystal Growth & Design
T2  - Crystal Growth & DesignCrystal Growth & Design
T1  - Supplementary data for the article: Ristić, P.; Todorović, T. R.; Blagojević, V.; Klisurić, O. R.; Marjanović, I.; Holló, B. B.; Vulić, P.; Gulea, M.; Donnard, M.; Monge, M.; Rodríguez-Castillo, M.; López-de-Luzuriaga, J. M.; Filipović, N. R. 1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-Carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study. Crystal Growth & Design 2020, 20 (7), 4461–4478. https://doi.org/10.1021/acs.cgd.0c00287
ER  - 
@misc{
author = "Ristić, Predrag and Todorović, Tamara and Blagojević, Vladimir A. and Klisurić, Olivera and Marjanović, Ivana and Holló, Berta Barta and Vulić, Predrag J. and Gulea, Mihaela and Donnard, Morgan and Monge, Miguel and Rodríguez-Castillo, María and López-de-Luzuriaga, José M. and Filipović, Nenad R.",
year = "2020",
publisher = "American Chemical Society",
journal = "Crystal Growth & Design, Crystal Growth & DesignCrystal Growth & Design",
title = "Supplementary data for the article: Ristić, P.; Todorović, T. R.; Blagojević, V.; Klisurić, O. R.; Marjanović, I.; Holló, B. B.; Vulić, P.; Gulea, M.; Donnard, M.; Monge, M.; Rodríguez-Castillo, M.; López-de-Luzuriaga, J. M.; Filipović, N. R. 1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-Carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study. Crystal Growth & Design 2020, 20 (7), 4461–4478. https://doi.org/10.1021/acs.cgd.0c00287"
}
Ristić, P., Todorović, T., Blagojević, V. A., Klisurić, O., Marjanović, I., Holló, B. B., Vulić, P. J., Gulea, M., Donnard, M., Monge, M., Rodríguez-Castillo, M., López-de-Luzuriaga, J. M.,& Filipović, N. R.. (2020). Supplementary data for the article: Ristić, P.; Todorović, T. R.; Blagojević, V.; Klisurić, O. R.; Marjanović, I.; Holló, B. B.; Vulić, P.; Gulea, M.; Donnard, M.; Monge, M.; Rodríguez-Castillo, M.; López-de-Luzuriaga, J. M.; Filipović, N. R. 1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-Carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study. Crystal Growth & Design 2020, 20 (7), 4461–4478. https://doi.org/10.1021/acs.cgd.0c00287. in Crystal Growth & Design
American Chemical Society..
Ristić P, Todorović T, Blagojević VA, Klisurić O, Marjanović I, Holló BB, Vulić PJ, Gulea M, Donnard M, Monge M, Rodríguez-Castillo M, López-de-Luzuriaga JM, Filipović NR. Supplementary data for the article: Ristić, P.; Todorović, T. R.; Blagojević, V.; Klisurić, O. R.; Marjanović, I.; Holló, B. B.; Vulić, P.; Gulea, M.; Donnard, M.; Monge, M.; Rodríguez-Castillo, M.; López-de-Luzuriaga, J. M.; Filipović, N. R. 1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-Carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study. Crystal Growth & Design 2020, 20 (7), 4461–4478. https://doi.org/10.1021/acs.cgd.0c00287. in Crystal Growth & Design. 2020;..
Ristić, Predrag, Todorović, Tamara, Blagojević, Vladimir A., Klisurić, Olivera, Marjanović, Ivana, Holló, Berta Barta, Vulić, Predrag J., Gulea, Mihaela, Donnard, Morgan, Monge, Miguel, Rodríguez-Castillo, María, López-de-Luzuriaga, José M., Filipović, Nenad R., "Supplementary data for the article: Ristić, P.; Todorović, T. R.; Blagojević, V.; Klisurić, O. R.; Marjanović, I.; Holló, B. B.; Vulić, P.; Gulea, M.; Donnard, M.; Monge, M.; Rodríguez-Castillo, M.; López-de-Luzuriaga, J. M.; Filipović, N. R. 1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-Carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study. Crystal Growth & Design 2020, 20 (7), 4461–4478. https://doi.org/10.1021/acs.cgd.0c00287" in Crystal Growth & Design (2020).

Influence of paleoenvironmental conditions on distribution and relative abundance of saturated and aromatic hydrocarbons in sediments from the NW part of the Toplica basin, Serbia

Burazer, Nikola; Šajnović, Aleksandra; Vasić, Nebojša; Kašanin-Grubin, Milica; Životić, Dragana R.; Mendonça Filho, João Graciano; Vulić, Predrag J.; Jovančićević, Branimir

(Elsevier, 2020)

TY  - JOUR
AU  - Burazer, Nikola
AU  - Šajnović, Aleksandra
AU  - Vasić, Nebojša
AU  - Kašanin-Grubin, Milica
AU  - Životić, Dragana R.
AU  - Mendonça Filho, João Graciano
AU  - Vulić, Predrag J.
AU  - Jovančićević, Branimir
PY  - 2020
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3837
AB  - The investigation of the relationship between paleoenvironmental conditions and distribution and relative abundance of specific saturated and aromatic hydrocarbons was the main objective of this study, thus marking the parameters, which were most sensitive to environmental changes. Insights on the type, generative potential, and maturity of organic matter (OM), as well as paleoclimate conditions, along with the reconstruction of depositional settings of the northwest part of the Toplica basin (Serbia), were provided. Organic petrographic, palynofacies, organic geochemical, mineralogical, and XRF analyses were carried out to investigate 40 sediment samples of the Prebreza and Čučale sedimentary units. Investigated samples were deposited in the saline and anoxic environment, under semi-arid to semi-humid/humid climate conditions, along with the constant inflow of volcanoclastic material. The predominance of δ-methyltrimethyltridecil chroman (δ-MTTC) within euxinic portions of the stratified water column was associated with an increase in salinity, which was noticed for sediments of the Prebreza unit. Sediments from this stratigraphic unit showed a higher contribution of algae precursor, whereas sediments of the Čučale unit suggested higher participation of microbiologically reworked OM. Most of the samples contained oil-prone kerogen type II. Maturity of the OM for sediments of the Prebreza unit ranged from immature to early-mature, while for samples of the Čučale unit varied from early-mature to mature stages. Distribution of hopane biomarkers typical for crude oil indicated that depth of 1 km was a boundary for the genesis of thermodynamic, more stable compounds. A significant portion of semifusinite was correlated with the paleofire event, which affected the distribution of n-alkanes. The high production of hydrocarbons was related to volcanic activity. Parameters, which proved to be highly susceptible at the stratigraphic boundary between the Prebreza and Čučale units, were C-value, S/H, α-MTTC, δ-MTTC, β-/γ-MTTC, and (1,3- + 1,6-)/(1,4 + 1,5-DMC), respectively.
PB  - Elsevier
T2  - Marine and Petroleum Geology
T1  - Influence of paleoenvironmental conditions on distribution and relative abundance of saturated and aromatic hydrocarbons in sediments from the NW part of the Toplica basin, Serbia
VL  - 115
SP  - 104252
DO  - 10.1016/j.marpetgeo.2020.104252
ER  - 
@article{
author = "Burazer, Nikola and Šajnović, Aleksandra and Vasić, Nebojša and Kašanin-Grubin, Milica and Životić, Dragana R. and Mendonça Filho, João Graciano and Vulić, Predrag J. and Jovančićević, Branimir",
year = "2020",
abstract = "The investigation of the relationship between paleoenvironmental conditions and distribution and relative abundance of specific saturated and aromatic hydrocarbons was the main objective of this study, thus marking the parameters, which were most sensitive to environmental changes. Insights on the type, generative potential, and maturity of organic matter (OM), as well as paleoclimate conditions, along with the reconstruction of depositional settings of the northwest part of the Toplica basin (Serbia), were provided. Organic petrographic, palynofacies, organic geochemical, mineralogical, and XRF analyses were carried out to investigate 40 sediment samples of the Prebreza and Čučale sedimentary units. Investigated samples were deposited in the saline and anoxic environment, under semi-arid to semi-humid/humid climate conditions, along with the constant inflow of volcanoclastic material. The predominance of δ-methyltrimethyltridecil chroman (δ-MTTC) within euxinic portions of the stratified water column was associated with an increase in salinity, which was noticed for sediments of the Prebreza unit. Sediments from this stratigraphic unit showed a higher contribution of algae precursor, whereas sediments of the Čučale unit suggested higher participation of microbiologically reworked OM. Most of the samples contained oil-prone kerogen type II. Maturity of the OM for sediments of the Prebreza unit ranged from immature to early-mature, while for samples of the Čučale unit varied from early-mature to mature stages. Distribution of hopane biomarkers typical for crude oil indicated that depth of 1 km was a boundary for the genesis of thermodynamic, more stable compounds. A significant portion of semifusinite was correlated with the paleofire event, which affected the distribution of n-alkanes. The high production of hydrocarbons was related to volcanic activity. Parameters, which proved to be highly susceptible at the stratigraphic boundary between the Prebreza and Čučale units, were C-value, S/H, α-MTTC, δ-MTTC, β-/γ-MTTC, and (1,3- + 1,6-)/(1,4 + 1,5-DMC), respectively.",
publisher = "Elsevier",
journal = "Marine and Petroleum Geology",
title = "Influence of paleoenvironmental conditions on distribution and relative abundance of saturated and aromatic hydrocarbons in sediments from the NW part of the Toplica basin, Serbia",
volume = "115",
pages = "104252",
doi = "10.1016/j.marpetgeo.2020.104252"
}
Burazer, N., Šajnović, A., Vasić, N., Kašanin-Grubin, M., Životić, D. R., Mendonça Filho, J. G., Vulić, P. J.,& Jovančićević, B.. (2020). Influence of paleoenvironmental conditions on distribution and relative abundance of saturated and aromatic hydrocarbons in sediments from the NW part of the Toplica basin, Serbia. in Marine and Petroleum Geology
Elsevier., 115, 104252.
https://doi.org/10.1016/j.marpetgeo.2020.104252
Burazer N, Šajnović A, Vasić N, Kašanin-Grubin M, Životić DR, Mendonça Filho JG, Vulić PJ, Jovančićević B. Influence of paleoenvironmental conditions on distribution and relative abundance of saturated and aromatic hydrocarbons in sediments from the NW part of the Toplica basin, Serbia. in Marine and Petroleum Geology. 2020;115:104252.
doi:10.1016/j.marpetgeo.2020.104252 .
Burazer, Nikola, Šajnović, Aleksandra, Vasić, Nebojša, Kašanin-Grubin, Milica, Životić, Dragana R., Mendonça Filho, João Graciano, Vulić, Predrag J., Jovančićević, Branimir, "Influence of paleoenvironmental conditions on distribution and relative abundance of saturated and aromatic hydrocarbons in sediments from the NW part of the Toplica basin, Serbia" in Marine and Petroleum Geology, 115 (2020):104252,
https://doi.org/10.1016/j.marpetgeo.2020.104252 . .
4
4
4

One-pot combustion synthesis of nickel oxide and hematite: From simple coordination compounds to high purity metal oxide nanoparticles

Jeremić, Dejan; Anđelković, Ljubica; Milenković, Milica R.; Šuljagić, Marija; Šumar-Ristović, Maja; Ostojić, Sanja; Nikolić, Aleksandar S.; Vulić, Predrag; Brčeski, Ilija; Pavlović, Vladimir B.

(2020)

TY  - JOUR
AU  - Jeremić, Dejan
AU  - Anđelković, Ljubica
AU  - Milenković, Milica R.
AU  - Šuljagić, Marija
AU  - Šumar-Ristović, Maja
AU  - Ostojić, Sanja
AU  - Nikolić, Aleksandar S.
AU  - Vulić, Predrag
AU  - Brčeski, Ilija
AU  - Pavlović, Vladimir B.
PY  - 2020
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/4306
AB  - This work is the first report of a very simple and fast one-pot synthesis of nickel oxide (NiO) and hematite (α-Fe2O3) nanoparticles by thermal decomposition of transition metal aqua complexes with camphor sulfonate anions. Obtained nanopowders were characterized by X-ray powder diffraction, Fourier transform IR analysis, scanning electron microscopy, and Energy-dispersive X-ray spectroscopy. X-ray powder diffraction confirmed the formation of high purity NiO and α-Fe2O3 crystal phases. In the case of α-Fe2O3, about five times larger average crystallite size was obtained. Fourier transform IR spectra of synthesized materials showed characteristic peaks for NiO and α-Fe2O3 nanostructures. To visualize the morphology and the chemical composition of the final products Scanning electron microscopy and Energy-dispersive X-ray spectroscopy were performed. The thermogravimetric analysis was done for a better understanding of the general thermal behavior of precursor compounds. This easy-to-perform and fast preparation method opens a broad range of obtained materials’ usage, particularly due to its economic viability
T2  - Science of Sintering
T1  - One-pot combustion synthesis of nickel oxide and hematite: From simple coordination compounds to high purity metal oxide nanoparticles
VL  - 52
IS  - 4
SP  - 481
EP  - 490
DO  - 10.2298/SOS2004481J
ER  - 
@article{
author = "Jeremić, Dejan and Anđelković, Ljubica and Milenković, Milica R. and Šuljagić, Marija and Šumar-Ristović, Maja and Ostojić, Sanja and Nikolić, Aleksandar S. and Vulić, Predrag and Brčeski, Ilija and Pavlović, Vladimir B.",
year = "2020",
abstract = "This work is the first report of a very simple and fast one-pot synthesis of nickel oxide (NiO) and hematite (α-Fe2O3) nanoparticles by thermal decomposition of transition metal aqua complexes with camphor sulfonate anions. Obtained nanopowders were characterized by X-ray powder diffraction, Fourier transform IR analysis, scanning electron microscopy, and Energy-dispersive X-ray spectroscopy. X-ray powder diffraction confirmed the formation of high purity NiO and α-Fe2O3 crystal phases. In the case of α-Fe2O3, about five times larger average crystallite size was obtained. Fourier transform IR spectra of synthesized materials showed characteristic peaks for NiO and α-Fe2O3 nanostructures. To visualize the morphology and the chemical composition of the final products Scanning electron microscopy and Energy-dispersive X-ray spectroscopy were performed. The thermogravimetric analysis was done for a better understanding of the general thermal behavior of precursor compounds. This easy-to-perform and fast preparation method opens a broad range of obtained materials’ usage, particularly due to its economic viability",
journal = "Science of Sintering",
title = "One-pot combustion synthesis of nickel oxide and hematite: From simple coordination compounds to high purity metal oxide nanoparticles",
volume = "52",
number = "4",
pages = "481-490",
doi = "10.2298/SOS2004481J"
}
Jeremić, D., Anđelković, L., Milenković, M. R., Šuljagić, M., Šumar-Ristović, M., Ostojić, S., Nikolić, A. S., Vulić, P., Brčeski, I.,& Pavlović, V. B.. (2020). One-pot combustion synthesis of nickel oxide and hematite: From simple coordination compounds to high purity metal oxide nanoparticles. in Science of Sintering, 52(4), 481-490.
https://doi.org/10.2298/SOS2004481J
Jeremić D, Anđelković L, Milenković MR, Šuljagić M, Šumar-Ristović M, Ostojić S, Nikolić AS, Vulić P, Brčeski I, Pavlović VB. One-pot combustion synthesis of nickel oxide and hematite: From simple coordination compounds to high purity metal oxide nanoparticles. in Science of Sintering. 2020;52(4):481-490.
doi:10.2298/SOS2004481J .
Jeremić, Dejan, Anđelković, Ljubica, Milenković, Milica R., Šuljagić, Marija, Šumar-Ristović, Maja, Ostojić, Sanja, Nikolić, Aleksandar S., Vulić, Predrag, Brčeski, Ilija, Pavlović, Vladimir B., "One-pot combustion synthesis of nickel oxide and hematite: From simple coordination compounds to high purity metal oxide nanoparticles" in Science of Sintering, 52, no. 4 (2020):481-490,
https://doi.org/10.2298/SOS2004481J . .
1
1
3

Oxidative degradation of aromatic N-compounds using cobalt containing montmorillonite-based catalysts

Ilić, Ilija; Milutinović-Nikolić, Aleksandra D.; Mojović, Zorica D.; Vuković, Zoran; Vulić, Predrag J.; Gržetić, Ivan; Banković, Predrag; Jović-Jovičić, Nataša

(Elsevier, 2020)

TY  - JOUR
AU  - Ilić, Ilija
AU  - Milutinović-Nikolić, Aleksandra D.
AU  - Mojović, Zorica D.
AU  - Vuković, Zoran
AU  - Vulić, Predrag J.
AU  - Gržetić, Ivan
AU  - Banković, Predrag
AU  - Jović-Jovičić, Nataša
PY  - 2020
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/4045
AB  - The goal of this work was the synthesis of a montmorillonite based catalyst for advanced oxidative degradation of organic water pollutants. Montmorillonite (Mt) –rich bentonite was acid-activated (MtA), and impregnated with cobalt (II) solution using the incipient wetness impregnation method. The impregnation was followed by heat treatment. Cobalt(II) ions were added in the quantities corresponding to 0.5 and 1.0 of the cation exchange capacity value. All samples were characterized by using chemical analysis, X-ray powder diffraction (XRPD), Electron paramagnetic resonance (EPR), X-ray photoelectron spectroscopy (XPS), Scanning electron microscopy (SEM) coupled with Energy-dispersive X-ray spectroscopy (EDS), Transmission electron microscopy (TEM) and low temperature N2 physisorption. The incorporation of the cobalt in the impregnated samples and the development of porous structure in the acid-activated ones were confirmed. The montmorillonite (Mt) was used as a catalyst support, while the cobalt in its oxide form was responsible for the generation of sulfo-radicals from Oxone®. Two aromatic N-compounds were tested as model pollutants: diazo dye - Acid Orange 10 (AO10) and nicotine. It was found that the synthesized catalysts could be used for the degradation of both pollutants, although more efficiently in AO10 degradation. The acid activation, higher cobalt loading, and temperature were found to be beneficial for the degradation of AO10.
PB  - Elsevier
T2  - Applied Clay Science
T1  - Oxidative degradation of aromatic N-compounds using cobalt containing montmorillonite-based catalysts
VL  - 193
SP  - 105668
DO  - 10.1016/j.clay.2020.105668
ER  - 
@article{
author = "Ilić, Ilija and Milutinović-Nikolić, Aleksandra D. and Mojović, Zorica D. and Vuković, Zoran and Vulić, Predrag J. and Gržetić, Ivan and Banković, Predrag and Jović-Jovičić, Nataša",
year = "2020",
abstract = "The goal of this work was the synthesis of a montmorillonite based catalyst for advanced oxidative degradation of organic water pollutants. Montmorillonite (Mt) –rich bentonite was acid-activated (MtA), and impregnated with cobalt (II) solution using the incipient wetness impregnation method. The impregnation was followed by heat treatment. Cobalt(II) ions were added in the quantities corresponding to 0.5 and 1.0 of the cation exchange capacity value. All samples were characterized by using chemical analysis, X-ray powder diffraction (XRPD), Electron paramagnetic resonance (EPR), X-ray photoelectron spectroscopy (XPS), Scanning electron microscopy (SEM) coupled with Energy-dispersive X-ray spectroscopy (EDS), Transmission electron microscopy (TEM) and low temperature N2 physisorption. The incorporation of the cobalt in the impregnated samples and the development of porous structure in the acid-activated ones were confirmed. The montmorillonite (Mt) was used as a catalyst support, while the cobalt in its oxide form was responsible for the generation of sulfo-radicals from Oxone®. Two aromatic N-compounds were tested as model pollutants: diazo dye - Acid Orange 10 (AO10) and nicotine. It was found that the synthesized catalysts could be used for the degradation of both pollutants, although more efficiently in AO10 degradation. The acid activation, higher cobalt loading, and temperature were found to be beneficial for the degradation of AO10.",
publisher = "Elsevier",
journal = "Applied Clay Science",
title = "Oxidative degradation of aromatic N-compounds using cobalt containing montmorillonite-based catalysts",
volume = "193",
pages = "105668",
doi = "10.1016/j.clay.2020.105668"
}
Ilić, I., Milutinović-Nikolić, A. D., Mojović, Z. D., Vuković, Z., Vulić, P. J., Gržetić, I., Banković, P.,& Jović-Jovičić, N.. (2020). Oxidative degradation of aromatic N-compounds using cobalt containing montmorillonite-based catalysts. in Applied Clay Science
Elsevier., 193, 105668.
https://doi.org/10.1016/j.clay.2020.105668
Ilić I, Milutinović-Nikolić AD, Mojović ZD, Vuković Z, Vulić PJ, Gržetić I, Banković P, Jović-Jovičić N. Oxidative degradation of aromatic N-compounds using cobalt containing montmorillonite-based catalysts. in Applied Clay Science. 2020;193:105668.
doi:10.1016/j.clay.2020.105668 .
Ilić, Ilija, Milutinović-Nikolić, Aleksandra D., Mojović, Zorica D., Vuković, Zoran, Vulić, Predrag J., Gržetić, Ivan, Banković, Predrag, Jović-Jovičić, Nataša, "Oxidative degradation of aromatic N-compounds using cobalt containing montmorillonite-based catalysts" in Applied Clay Science, 193 (2020):105668,
https://doi.org/10.1016/j.clay.2020.105668 . .
3
1

Supplementary data for the article: Ilić, I.; Milutinović-Nikolić, A.; Mojović, Z.; Vuković, Z.; Vulić, P.; Gržetić, I.; Banković, P.; Jović-Jovičić, N. Oxidative Degradation of Aromatic N-Compounds Using Cobalt Containing Montmorillonite-Based Catalysts. Applied Clay Science 2020, 193, 105668. https://doi.org/10.1016/j.clay.2020.105668

Ilić, Ilija; Milutinović-Nikolić, Aleksandra D.; Mojović, Zorica D.; Vuković, Zoran; Vulić, Predrag J.; Gržetić, Ivan; Banković, Predrag; Jović-Jovičić, Nataša

(Elsevier, 2020)

TY  - DATA
AU  - Ilić, Ilija
AU  - Milutinović-Nikolić, Aleksandra D.
AU  - Mojović, Zorica D.
AU  - Vuković, Zoran
AU  - Vulić, Predrag J.
AU  - Gržetić, Ivan
AU  - Banković, Predrag
AU  - Jović-Jovičić, Nataša
PY  - 2020
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/4046
PB  - Elsevier
T2  - Applied Clay Science
T1  - Supplementary data for the article: Ilić, I.; Milutinović-Nikolić, A.; Mojović, Z.; Vuković, Z.; Vulić, P.; Gržetić, I.; Banković, P.; Jović-Jovičić, N. Oxidative Degradation of Aromatic N-Compounds Using Cobalt Containing Montmorillonite-Based Catalysts. Applied Clay Science 2020, 193, 105668. https://doi.org/10.1016/j.clay.2020.105668
ER  - 
@misc{
author = "Ilić, Ilija and Milutinović-Nikolić, Aleksandra D. and Mojović, Zorica D. and Vuković, Zoran and Vulić, Predrag J. and Gržetić, Ivan and Banković, Predrag and Jović-Jovičić, Nataša",
year = "2020",
publisher = "Elsevier",
journal = "Applied Clay Science",
title = "Supplementary data for the article: Ilić, I.; Milutinović-Nikolić, A.; Mojović, Z.; Vuković, Z.; Vulić, P.; Gržetić, I.; Banković, P.; Jović-Jovičić, N. Oxidative Degradation of Aromatic N-Compounds Using Cobalt Containing Montmorillonite-Based Catalysts. Applied Clay Science 2020, 193, 105668. https://doi.org/10.1016/j.clay.2020.105668"
}
Ilić, I., Milutinović-Nikolić, A. D., Mojović, Z. D., Vuković, Z., Vulić, P. J., Gržetić, I., Banković, P.,& Jović-Jovičić, N.. (2020). Supplementary data for the article: Ilić, I.; Milutinović-Nikolić, A.; Mojović, Z.; Vuković, Z.; Vulić, P.; Gržetić, I.; Banković, P.; Jović-Jovičić, N. Oxidative Degradation of Aromatic N-Compounds Using Cobalt Containing Montmorillonite-Based Catalysts. Applied Clay Science 2020, 193, 105668. https://doi.org/10.1016/j.clay.2020.105668. in Applied Clay Science
Elsevier..
Ilić I, Milutinović-Nikolić AD, Mojović ZD, Vuković Z, Vulić PJ, Gržetić I, Banković P, Jović-Jovičić N. Supplementary data for the article: Ilić, I.; Milutinović-Nikolić, A.; Mojović, Z.; Vuković, Z.; Vulić, P.; Gržetić, I.; Banković, P.; Jović-Jovičić, N. Oxidative Degradation of Aromatic N-Compounds Using Cobalt Containing Montmorillonite-Based Catalysts. Applied Clay Science 2020, 193, 105668. https://doi.org/10.1016/j.clay.2020.105668. in Applied Clay Science. 2020;..
Ilić, Ilija, Milutinović-Nikolić, Aleksandra D., Mojović, Zorica D., Vuković, Zoran, Vulić, Predrag J., Gržetić, Ivan, Banković, Predrag, Jović-Jovičić, Nataša, "Supplementary data for the article: Ilić, I.; Milutinović-Nikolić, A.; Mojović, Z.; Vuković, Z.; Vulić, P.; Gržetić, I.; Banković, P.; Jović-Jovičić, N. Oxidative Degradation of Aromatic N-Compounds Using Cobalt Containing Montmorillonite-Based Catalysts. Applied Clay Science 2020, 193, 105668. https://doi.org/10.1016/j.clay.2020.105668" in Applied Clay Science (2020).

Distribution of major and trace elements in the Kovin lignite (Serbia)

Životić, Dragana R.; Cvetković, Olga; Vulić, Predrag J.; Gržetić, Ivan; Simić, Vladimir; Ilijević, Konstantin; Dojčinović, Biljana P.; Erić, Suzana; Radić, Bogdan; Stojadinović, Sanja; Trifunović, Snežana S.

(Crossref, 2019)

TY  - JOUR
AU  - Životić, Dragana R.
AU  - Cvetković, Olga
AU  - Vulić, Predrag J.
AU  - Gržetić, Ivan
AU  - Simić, Vladimir
AU  - Ilijević, Konstantin
AU  - Dojčinović, Biljana P.
AU  - Erić, Suzana
AU  - Radić, Bogdan
AU  - Stojadinović, Sanja
AU  - Trifunović, Snežana S.
PY  - 2019
PY  - 2019
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2897
AB  - A geochemical and mineralogical study was performed on lignite samples from the Upper Miocene Kovin deposit, hosting three coal seams. The Kovin lignite is characterized by high moisture content, medium to high ash yield, medium to high sulphur content and a relatively low gross and net calorific value. The mineralogical composition, and major and trace element contents were determined by X-ray diffraction, scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDS) analyses, and inductively coupled plasma optical emission spectrometry (ICP-OES). The most abundant minerals in all lignite samples from the three coal seams are clays (illite/smectite), silicates (quartz, plagioclase), sulphates (gypsum/anhydrite) and carbonate (calcite). The other iron-rich minerals are sulphides, oxides and hydroxides (pyrite, mag-netite, haematite, and limonite). In general, mineral matter in the matrix coal consists of illite/ smectite and quartz, while xylite-rich coals, apart from illite/smectite, have a higher content of sulphates and Fe-oxide/hydroxide minerals. The lignite from the Kovin deposit is enriched in As, Cd, Co, Cr, Cu, Ga, Li, Mn, Mo, Ni, Pb, V, Zn, Gd, Tb, Er and Lu in comparison with the Clarke values for brown coals. The statistical analysis of bulk compositional data shows inorganic affinity for the majority of the major and trace elements and possible association with pyrite, illite/ smectite and calcite.
PB  - Crossref
T2  - Geologia Croatica
T1  - Distribution of major and trace elements in the Kovin lignite (Serbia)
VL  - 72
IS  - 1
SP  - 51
EP  - 79
DO  - 10.4154/gc.2019.06
ER  - 
@article{
author = "Životić, Dragana R. and Cvetković, Olga and Vulić, Predrag J. and Gržetić, Ivan and Simić, Vladimir and Ilijević, Konstantin and Dojčinović, Biljana P. and Erić, Suzana and Radić, Bogdan and Stojadinović, Sanja and Trifunović, Snežana S.",
year = "2019, 2019",
abstract = "A geochemical and mineralogical study was performed on lignite samples from the Upper Miocene Kovin deposit, hosting three coal seams. The Kovin lignite is characterized by high moisture content, medium to high ash yield, medium to high sulphur content and a relatively low gross and net calorific value. The mineralogical composition, and major and trace element contents were determined by X-ray diffraction, scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDS) analyses, and inductively coupled plasma optical emission spectrometry (ICP-OES). The most abundant minerals in all lignite samples from the three coal seams are clays (illite/smectite), silicates (quartz, plagioclase), sulphates (gypsum/anhydrite) and carbonate (calcite). The other iron-rich minerals are sulphides, oxides and hydroxides (pyrite, mag-netite, haematite, and limonite). In general, mineral matter in the matrix coal consists of illite/ smectite and quartz, while xylite-rich coals, apart from illite/smectite, have a higher content of sulphates and Fe-oxide/hydroxide minerals. The lignite from the Kovin deposit is enriched in As, Cd, Co, Cr, Cu, Ga, Li, Mn, Mo, Ni, Pb, V, Zn, Gd, Tb, Er and Lu in comparison with the Clarke values for brown coals. The statistical analysis of bulk compositional data shows inorganic affinity for the majority of the major and trace elements and possible association with pyrite, illite/ smectite and calcite.",
publisher = "Crossref",
journal = "Geologia Croatica",
title = "Distribution of major and trace elements in the Kovin lignite (Serbia)",
volume = "72",
number = "1",
pages = "51-79",
doi = "10.4154/gc.2019.06"
}
Životić, D. R., Cvetković, O., Vulić, P. J., Gržetić, I., Simić, V., Ilijević, K., Dojčinović, B. P., Erić, S., Radić, B., Stojadinović, S.,& Trifunović, S. S.. (2019). Distribution of major and trace elements in the Kovin lignite (Serbia). in Geologia Croatica
Crossref., 72(1), 51-79.
https://doi.org/10.4154/gc.2019.06
Životić DR, Cvetković O, Vulić PJ, Gržetić I, Simić V, Ilijević K, Dojčinović BP, Erić S, Radić B, Stojadinović S, Trifunović SS. Distribution of major and trace elements in the Kovin lignite (Serbia). in Geologia Croatica. 2019;72(1):51-79.
doi:10.4154/gc.2019.06 .
Životić, Dragana R., Cvetković, Olga, Vulić, Predrag J., Gržetić, Ivan, Simić, Vladimir, Ilijević, Konstantin, Dojčinović, Biljana P., Erić, Suzana, Radić, Bogdan, Stojadinović, Sanja, Trifunović, Snežana S., "Distribution of major and trace elements in the Kovin lignite (Serbia)" in Geologia Croatica, 72, no. 1 (2019):51-79,
https://doi.org/10.4154/gc.2019.06 . .
4
4
3

Optical evidence of magnetic field-induced ferrofluid aggregation: Comparison of cobalt ferrite, magnetite, and magnesium ferrite

Lakić, Mladen; Anđelković, Ljubica; Šuljagić, Marija; Vulić, Predrag J.; Perić, Marko; Iskrenović, Predrag; Krstić, Ivan; Kuraica, Milorad M.; Nikolić, Aleksandar S.

(Elsevier, 2019)

TY  - JOUR
AU  - Lakić, Mladen
AU  - Anđelković, Ljubica
AU  - Šuljagić, Marija
AU  - Vulić, Predrag J.
AU  - Perić, Marko
AU  - Iskrenović, Predrag
AU  - Krstić, Ivan
AU  - Kuraica, Milorad M.
AU  - Nikolić, Aleksandar S.
PY  - 2019
AB  - Light-transmitting measurements of white light and a consequentially chosen laser beam of 655 nm propagating through citrate- and oleate-coated CoFe 2 O 4 , FeFe 2 O 4 and MgFe 2 O 4 nanoparticles under the influence of an external magnetic field were presented. New experimental settings were developed for the optical study of ferrites’ behavior in ferrofluid with the applied magnetic field strength within the 30–400 mT range. A magnetic field-induced change of light transmittance occurred and a precipitation of all studied samples was obtained. Optical investigations of ferrofluid suspensions revealed that, contrary to the linear aggregates of colloidal CoFe 2 O 4 and FeFe 2 O 4 , spheroidal aggregates were formed in the case of MgFe 2 O 4 . In all three cases, the surface modification resulted in decreased dipole–dipole interactions between ferrite cores, and thus, less precipitates were noticed. All oleate-coated nanoparticles have demonstrated weaker magnetic responses compared to the citrate-encapsulated samples. The aggregation of nanoparticles potentially increases cytotoxicity. Regarding non-linear clustering of MgFe 2 O 4 suspensions, it can be concluded that its excretion from the organism may likely be easier and faster when used in diagnosis and/or therapy. Therefore, more attention should be paid to the lowly toxic MgFe 2 O 4 regarding its medical application.
PB  - Elsevier
T2  - Optical Materials
T1  - Optical evidence of magnetic field-induced ferrofluid aggregation: Comparison of cobalt ferrite, magnetite, and magnesium ferrite
VL  - 91
SP  - 279
EP  - 285
DO  - 10.1016/j.optmat.2019.03.031
ER  - 
@article{
author = "Lakić, Mladen and Anđelković, Ljubica and Šuljagić, Marija and Vulić, Predrag J. and Perić, Marko and Iskrenović, Predrag and Krstić, Ivan and Kuraica, Milorad M. and Nikolić, Aleksandar S.",
year = "2019",
abstract = "Light-transmitting measurements of white light and a consequentially chosen laser beam of 655 nm propagating through citrate- and oleate-coated CoFe 2 O 4 , FeFe 2 O 4 and MgFe 2 O 4 nanoparticles under the influence of an external magnetic field were presented. New experimental settings were developed for the optical study of ferrites’ behavior in ferrofluid with the applied magnetic field strength within the 30–400 mT range. A magnetic field-induced change of light transmittance occurred and a precipitation of all studied samples was obtained. Optical investigations of ferrofluid suspensions revealed that, contrary to the linear aggregates of colloidal CoFe 2 O 4 and FeFe 2 O 4 , spheroidal aggregates were formed in the case of MgFe 2 O 4 . In all three cases, the surface modification resulted in decreased dipole–dipole interactions between ferrite cores, and thus, less precipitates were noticed. All oleate-coated nanoparticles have demonstrated weaker magnetic responses compared to the citrate-encapsulated samples. The aggregation of nanoparticles potentially increases cytotoxicity. Regarding non-linear clustering of MgFe 2 O 4 suspensions, it can be concluded that its excretion from the organism may likely be easier and faster when used in diagnosis and/or therapy. Therefore, more attention should be paid to the lowly toxic MgFe 2 O 4 regarding its medical application.",
publisher = "Elsevier",
journal = "Optical Materials",
title = "Optical evidence of magnetic field-induced ferrofluid aggregation: Comparison of cobalt ferrite, magnetite, and magnesium ferrite",
volume = "91",
pages = "279-285",
doi = "10.1016/j.optmat.2019.03.031"
}
Lakić, M., Anđelković, L., Šuljagić, M., Vulić, P. J., Perić, M., Iskrenović, P., Krstić, I., Kuraica, M. M.,& Nikolić, A. S.. (2019). Optical evidence of magnetic field-induced ferrofluid aggregation: Comparison of cobalt ferrite, magnetite, and magnesium ferrite. in Optical Materials
Elsevier., 91, 279-285.
https://doi.org/10.1016/j.optmat.2019.03.031
Lakić M, Anđelković L, Šuljagić M, Vulić PJ, Perić M, Iskrenović P, Krstić I, Kuraica MM, Nikolić AS. Optical evidence of magnetic field-induced ferrofluid aggregation: Comparison of cobalt ferrite, magnetite, and magnesium ferrite. in Optical Materials. 2019;91:279-285.
doi:10.1016/j.optmat.2019.03.031 .
Lakić, Mladen, Anđelković, Ljubica, Šuljagić, Marija, Vulić, Predrag J., Perić, Marko, Iskrenović, Predrag, Krstić, Ivan, Kuraica, Milorad M., Nikolić, Aleksandar S., "Optical evidence of magnetic field-induced ferrofluid aggregation: Comparison of cobalt ferrite, magnetite, and magnesium ferrite" in Optical Materials, 91 (2019):279-285,
https://doi.org/10.1016/j.optmat.2019.03.031 . .
6
6
6

Anti-Hail Protection-Assessment of Financial Effects on the Territory of Belgrade

Vukelić, Gordana; Cvetković, Olga; Gržetić, Ivan; Simić, Miloš; Miodragović, Zoran; Lazić, Lazar; Zarić, Miroljub; Pešić, Aleksandar; Vulić, Predrag J.

(Mdpi, Basel, 2018)

TY  - JOUR
AU  - Vukelić, Gordana
AU  - Cvetković, Olga
AU  - Gržetić, Ivan
AU  - Simić, Miloš
AU  - Miodragović, Zoran
AU  - Lazić, Lazar
AU  - Zarić, Miroljub
AU  - Pešić, Aleksandar
AU  - Vulić, Predrag J.
PY  - 2018
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2159
AB  - The aim of this work is to assess damage to the City of Belgrade caused by the unfavorable weather condition of hail due to the absence of anti-hail defense of the city, and to argumentatively point out the necessity of introducing new technical-technological systems for preventing the effects of adverse weather conditions. The results are based on the direct correlation-analyses of two real unfavorable weather events and the estimated financial damage caused by these events. The overall calculation also takes into account financial investments (new financial model) necessary to establish two essentially different systems for anti-hail protection. The damage caused by the hail on the territory of the City of Belgrade and the financial investment in anti-hail protection to reduce it are empirically established for the first time. It is shown how the damage could be transformed to profit, as the financial investment in anti-hail protection is lower than the damage that hail can cause.
PB  - Mdpi, Basel
T2  - Sustainability
T1  - Anti-Hail Protection-Assessment of Financial Effects on the Territory of Belgrade
VL  - 10
IS  - 4
DO  - 10.3390/su10041239
UR  - Kon_3490
ER  - 
@article{
author = "Vukelić, Gordana and Cvetković, Olga and Gržetić, Ivan and Simić, Miloš and Miodragović, Zoran and Lazić, Lazar and Zarić, Miroljub and Pešić, Aleksandar and Vulić, Predrag J.",
year = "2018",
abstract = "The aim of this work is to assess damage to the City of Belgrade caused by the unfavorable weather condition of hail due to the absence of anti-hail defense of the city, and to argumentatively point out the necessity of introducing new technical-technological systems for preventing the effects of adverse weather conditions. The results are based on the direct correlation-analyses of two real unfavorable weather events and the estimated financial damage caused by these events. The overall calculation also takes into account financial investments (new financial model) necessary to establish two essentially different systems for anti-hail protection. The damage caused by the hail on the territory of the City of Belgrade and the financial investment in anti-hail protection to reduce it are empirically established for the first time. It is shown how the damage could be transformed to profit, as the financial investment in anti-hail protection is lower than the damage that hail can cause.",
publisher = "Mdpi, Basel",
journal = "Sustainability",
title = "Anti-Hail Protection-Assessment of Financial Effects on the Territory of Belgrade",
volume = "10",
number = "4",
doi = "10.3390/su10041239",
url = "Kon_3490"
}
Vukelić, G., Cvetković, O., Gržetić, I., Simić, M., Miodragović, Z., Lazić, L., Zarić, M., Pešić, A.,& Vulić, P. J.. (2018). Anti-Hail Protection-Assessment of Financial Effects on the Territory of Belgrade. in Sustainability
Mdpi, Basel., 10(4).
https://doi.org/10.3390/su10041239
Kon_3490
Vukelić G, Cvetković O, Gržetić I, Simić M, Miodragović Z, Lazić L, Zarić M, Pešić A, Vulić PJ. Anti-Hail Protection-Assessment of Financial Effects on the Territory of Belgrade. in Sustainability. 2018;10(4).
doi:10.3390/su10041239
Kon_3490 .
Vukelić, Gordana, Cvetković, Olga, Gržetić, Ivan, Simić, Miloš, Miodragović, Zoran, Lazić, Lazar, Zarić, Miroljub, Pešić, Aleksandar, Vulić, Predrag J., "Anti-Hail Protection-Assessment of Financial Effects on the Territory of Belgrade" in Sustainability, 10, no. 4 (2018),
https://doi.org/10.3390/su10041239 .,
Kon_3490 .
1
1
1

A study of the structural and morphological properties of Ni-ferrite, Zn-ferrite and Ni-Zn-ferrites functionalized with starch

Anđelković, Ljubica; Šuljagić, Marija; Lakić, Mladen; Jeremić, Dejan; Vulić, Predrag J.; Nikolić, Aleksandar S.

(Elsevier Sci Ltd, Oxford, 2018)

TY  - JOUR
AU  - Anđelković, Ljubica
AU  - Šuljagić, Marija
AU  - Lakić, Mladen
AU  - Jeremić, Dejan
AU  - Vulić, Predrag J.
AU  - Nikolić, Aleksandar S.
PY  - 2018
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2171
AB  - Zinc-ferrite, nickel-ferrite and mixed nickel-zinc ferrites were successfully synthesized via the thermal decomposition method from acetylacetonate complexes. To control the particle size and enhance dispersibility in an aqueous medium, starch, a natural and biocompatible compound, was used for the first time for coating such magnetic powders. X-ray powder diffraction (XRPD) was performed to study the structural properties of all samples. The presence of a single-phase spinel structure as well as the cation distribution in both sites of all investigated magnetic powders was confirmed. The values of unit cell parameters obtained from the results of the Rietveld analysis decreased, while the average crystallite size increased with increasing Ni2+ content. The average microstrain parameters unambiguously showed a change in the spinel structure with cation distribution. Scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS) and Fourier transform infrared spectroscopy (FTIR) analyses were also utilized to characterize the synthesized materials, corroborating the XRPD data. The obtained results indicated that functionalization by starch was successfully achieved.
PB  - Elsevier Sci Ltd, Oxford
T2  - Ceramics International
T1  - A study of the structural and morphological properties of Ni-ferrite, Zn-ferrite and Ni-Zn-ferrites functionalized with starch
VL  - 44
IS  - 12
SP  - 14163
EP  - 14168
DO  - 10.1016/j.ceramint.2018.05.018
UR  - Kon_3502
ER  - 
@article{
author = "Anđelković, Ljubica and Šuljagić, Marija and Lakić, Mladen and Jeremić, Dejan and Vulić, Predrag J. and Nikolić, Aleksandar S.",
year = "2018",
abstract = "Zinc-ferrite, nickel-ferrite and mixed nickel-zinc ferrites were successfully synthesized via the thermal decomposition method from acetylacetonate complexes. To control the particle size and enhance dispersibility in an aqueous medium, starch, a natural and biocompatible compound, was used for the first time for coating such magnetic powders. X-ray powder diffraction (XRPD) was performed to study the structural properties of all samples. The presence of a single-phase spinel structure as well as the cation distribution in both sites of all investigated magnetic powders was confirmed. The values of unit cell parameters obtained from the results of the Rietveld analysis decreased, while the average crystallite size increased with increasing Ni2+ content. The average microstrain parameters unambiguously showed a change in the spinel structure with cation distribution. Scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS) and Fourier transform infrared spectroscopy (FTIR) analyses were also utilized to characterize the synthesized materials, corroborating the XRPD data. The obtained results indicated that functionalization by starch was successfully achieved.",
publisher = "Elsevier Sci Ltd, Oxford",
journal = "Ceramics International",
title = "A study of the structural and morphological properties of Ni-ferrite, Zn-ferrite and Ni-Zn-ferrites functionalized with starch",
volume = "44",
number = "12",
pages = "14163-14168",
doi = "10.1016/j.ceramint.2018.05.018",
url = "Kon_3502"
}
Anđelković, L., Šuljagić, M., Lakić, M., Jeremić, D., Vulić, P. J.,& Nikolić, A. S.. (2018). A study of the structural and morphological properties of Ni-ferrite, Zn-ferrite and Ni-Zn-ferrites functionalized with starch. in Ceramics International
Elsevier Sci Ltd, Oxford., 44(12), 14163-14168.
https://doi.org/10.1016/j.ceramint.2018.05.018
Kon_3502
Anđelković L, Šuljagić M, Lakić M, Jeremić D, Vulić PJ, Nikolić AS. A study of the structural and morphological properties of Ni-ferrite, Zn-ferrite and Ni-Zn-ferrites functionalized with starch. in Ceramics International. 2018;44(12):14163-14168.
doi:10.1016/j.ceramint.2018.05.018
Kon_3502 .
Anđelković, Ljubica, Šuljagić, Marija, Lakić, Mladen, Jeremić, Dejan, Vulić, Predrag J., Nikolić, Aleksandar S., "A study of the structural and morphological properties of Ni-ferrite, Zn-ferrite and Ni-Zn-ferrites functionalized with starch" in Ceramics International, 44, no. 12 (2018):14163-14168,
https://doi.org/10.1016/j.ceramint.2018.05.018 .,
Kon_3502 .
34
33
34

A study of the structural and morphological properties of Ni-ferrite, Zn-ferrite and Ni-Zn-ferrites functionalized with starch

Anđelković, Ljubica; Šuljagić, Marija; Lakić, Mladen; Jeremić, Dejan; Vulić, Predrag J.; Nikolić, Aleksandar S.

(Elsevier Sci Ltd, Oxford, 2018)

TY  - JOUR
AU  - Anđelković, Ljubica
AU  - Šuljagić, Marija
AU  - Lakić, Mladen
AU  - Jeremić, Dejan
AU  - Vulić, Predrag J.
AU  - Nikolić, Aleksandar S.
PY  - 2018
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3149
AB  - Zinc-ferrite, nickel-ferrite and mixed nickel-zinc ferrites were successfully synthesized via the thermal decomposition method from acetylacetonate complexes. To control the particle size and enhance dispersibility in an aqueous medium, starch, a natural and biocompatible compound, was used for the first time for coating such magnetic powders. X-ray powder diffraction (XRPD) was performed to study the structural properties of all samples. The presence of a single-phase spinel structure as well as the cation distribution in both sites of all investigated magnetic powders was confirmed. The values of unit cell parameters obtained from the results of the Rietveld analysis decreased, while the average crystallite size increased with increasing Ni2+ content. The average microstrain parameters unambiguously showed a change in the spinel structure with cation distribution. Scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS) and Fourier transform infrared spectroscopy (FTIR) analyses were also utilized to characterize the synthesized materials, corroborating the XRPD data. The obtained results indicated that functionalization by starch was successfully achieved.
PB  - Elsevier Sci Ltd, Oxford
T2  - Ceramics International
T1  - A study of the structural and morphological properties of Ni-ferrite, Zn-ferrite and Ni-Zn-ferrites functionalized with starch
VL  - 44
IS  - 12
SP  - 14163
EP  - 14168
DO  - 10.1016/j.ceramint.2018.05.018
UR  - Kon_3502
ER  - 
@article{
author = "Anđelković, Ljubica and Šuljagić, Marija and Lakić, Mladen and Jeremić, Dejan and Vulić, Predrag J. and Nikolić, Aleksandar S.",
year = "2018",
abstract = "Zinc-ferrite, nickel-ferrite and mixed nickel-zinc ferrites were successfully synthesized via the thermal decomposition method from acetylacetonate complexes. To control the particle size and enhance dispersibility in an aqueous medium, starch, a natural and biocompatible compound, was used for the first time for coating such magnetic powders. X-ray powder diffraction (XRPD) was performed to study the structural properties of all samples. The presence of a single-phase spinel structure as well as the cation distribution in both sites of all investigated magnetic powders was confirmed. The values of unit cell parameters obtained from the results of the Rietveld analysis decreased, while the average crystallite size increased with increasing Ni2+ content. The average microstrain parameters unambiguously showed a change in the spinel structure with cation distribution. Scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS) and Fourier transform infrared spectroscopy (FTIR) analyses were also utilized to characterize the synthesized materials, corroborating the XRPD data. The obtained results indicated that functionalization by starch was successfully achieved.",
publisher = "Elsevier Sci Ltd, Oxford",
journal = "Ceramics International",
title = "A study of the structural and morphological properties of Ni-ferrite, Zn-ferrite and Ni-Zn-ferrites functionalized with starch",
volume = "44",
number = "12",
pages = "14163-14168",
doi = "10.1016/j.ceramint.2018.05.018",
url = "Kon_3502"
}
Anđelković, L., Šuljagić, M., Lakić, M., Jeremić, D., Vulić, P. J.,& Nikolić, A. S.. (2018). A study of the structural and morphological properties of Ni-ferrite, Zn-ferrite and Ni-Zn-ferrites functionalized with starch. in Ceramics International
Elsevier Sci Ltd, Oxford., 44(12), 14163-14168.
https://doi.org/10.1016/j.ceramint.2018.05.018
Kon_3502
Anđelković L, Šuljagić M, Lakić M, Jeremić D, Vulić PJ, Nikolić AS. A study of the structural and morphological properties of Ni-ferrite, Zn-ferrite and Ni-Zn-ferrites functionalized with starch. in Ceramics International. 2018;44(12):14163-14168.
doi:10.1016/j.ceramint.2018.05.018
Kon_3502 .
Anđelković, Ljubica, Šuljagić, Marija, Lakić, Mladen, Jeremić, Dejan, Vulić, Predrag J., Nikolić, Aleksandar S., "A study of the structural and morphological properties of Ni-ferrite, Zn-ferrite and Ni-Zn-ferrites functionalized with starch" in Ceramics International, 44, no. 12 (2018):14163-14168,
https://doi.org/10.1016/j.ceramint.2018.05.018 .,
Kon_3502 .
35
33
34

Effects of Gd3+ co-doping on NaYF4:Yb,Er nanoparticles structure

Vuković, Marina; Dinić, Ivana; Mančić, Lidija; Vulić, Predrag J.

(Belgrade : Serbian Ceramic Society, 2018)

TY  - CONF
AU  - Vuković, Marina
AU  - Dinić, Ivana
AU  - Mančić, Lidija
AU  - Vulić, Predrag J.
PY  - 2018
UR  - http://dais.sanu.ac.rs/123456789/4117
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2775
AB  - NaYF4 doped with Rare Earth elements such as Yb and Er is well known as a compound with the remarkable up-conversion photoluminesce and wide application. In this work, the influence of additional co-doping of NaYF4:Yb,Er with gadolinium (0, 15 and 30 mol%) was explored. The syntheses were performed solvothermally using the mixture of water/ethanol as medium and polyvinylpyrrolidone (PVP) as capping ligand. The obtained powders were subjected to X-ray powder diffraction (XRPD), scanning electron microscopy (SEM), Fourier-transform infrared (FTIR) spectroscopy and photoluminesce (PL) analyses. Structural refinement shown that NaYF4:Yb,Er particles generally crystallized in a cubic form (Fm-3m), while the additional presence of Gd3+ in the crystal lattice lead to the pure hexagonal phase crystallization (P63/m). Morphological analyses revealed that all powders are composed from nanodimensional particles with the size in the range of 50-70 nm, while FTIR spectra confirmed the presence of PVP functional groups on the particles surfaces. The strongest effect of Gd3+ doping was notices in the PL spectra, where the up-conversion response increases with the mol% of this dopant.
PB  - Belgrade : Serbian Ceramic Society
C3  - Program and the Book of Abstracts / Serbian Ceramic Society Conference Advanced Ceramics and Application VII : New Frontiers in Multifunctional Material Science and Processing, Serbia, Belgrade, 17-19 September 2018
T1  - Effects of Gd3+ co-doping on NaYF4:Yb,Er nanoparticles structure
SP  - 72
EP  - 72
ER  - 
@conference{
author = "Vuković, Marina and Dinić, Ivana and Mančić, Lidija and Vulić, Predrag J.",
year = "2018",
abstract = "NaYF4 doped with Rare Earth elements such as Yb and Er is well known as a compound with the remarkable up-conversion photoluminesce and wide application. In this work, the influence of additional co-doping of NaYF4:Yb,Er with gadolinium (0, 15 and 30 mol%) was explored. The syntheses were performed solvothermally using the mixture of water/ethanol as medium and polyvinylpyrrolidone (PVP) as capping ligand. The obtained powders were subjected to X-ray powder diffraction (XRPD), scanning electron microscopy (SEM), Fourier-transform infrared (FTIR) spectroscopy and photoluminesce (PL) analyses. Structural refinement shown that NaYF4:Yb,Er particles generally crystallized in a cubic form (Fm-3m), while the additional presence of Gd3+ in the crystal lattice lead to the pure hexagonal phase crystallization (P63/m). Morphological analyses revealed that all powders are composed from nanodimensional particles with the size in the range of 50-70 nm, while FTIR spectra confirmed the presence of PVP functional groups on the particles surfaces. The strongest effect of Gd3+ doping was notices in the PL spectra, where the up-conversion response increases with the mol% of this dopant.",
publisher = "Belgrade : Serbian Ceramic Society",
journal = "Program and the Book of Abstracts / Serbian Ceramic Society Conference Advanced Ceramics and Application VII : New Frontiers in Multifunctional Material Science and Processing, Serbia, Belgrade, 17-19 September 2018",
title = "Effects of Gd3+ co-doping on NaYF4:Yb,Er nanoparticles structure",
pages = "72-72"
}
Vuković, M., Dinić, I., Mančić, L.,& Vulić, P. J.. (2018). Effects of Gd3+ co-doping on NaYF4:Yb,Er nanoparticles structure. in Program and the Book of Abstracts / Serbian Ceramic Society Conference Advanced Ceramics and Application VII : New Frontiers in Multifunctional Material Science and Processing, Serbia, Belgrade, 17-19 September 2018
Belgrade : Serbian Ceramic Society., 72-72.
Vuković M, Dinić I, Mančić L, Vulić PJ. Effects of Gd3+ co-doping on NaYF4:Yb,Er nanoparticles structure. in Program and the Book of Abstracts / Serbian Ceramic Society Conference Advanced Ceramics and Application VII : New Frontiers in Multifunctional Material Science and Processing, Serbia, Belgrade, 17-19 September 2018. 2018;:72-72..
Vuković, Marina, Dinić, Ivana, Mančić, Lidija, Vulić, Predrag J., "Effects of Gd3+ co-doping on NaYF4:Yb,Er nanoparticles structure" in Program and the Book of Abstracts / Serbian Ceramic Society Conference Advanced Ceramics and Application VII : New Frontiers in Multifunctional Material Science and Processing, Serbia, Belgrade, 17-19 September 2018 (2018):72-72.

Amperometric ascorbic acid sensor based on doped ferrites nanoparticles modified glassy carbon paste electrode

Dimitrijević, Teodora; Vulić, Predrag J.; Manojlović, Dragan D.; Nikolić, Aleksandar S.; Stanković, Dalibor

(Academic Press Inc Elsevier Science, San Diego, 2016)

TY  - JOUR
AU  - Dimitrijević, Teodora
AU  - Vulić, Predrag J.
AU  - Manojlović, Dragan D.
AU  - Nikolić, Aleksandar S.
AU  - Stanković, Dalibor
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1950
AB  - In this study, a novel electrochemical sensor for quantification of ascorbic acid with amperometric detection in physiological conditions was constructed. For this purpose, cobalt and nickel ferrites were synthesized using microwave and ultrasound assistance, characterized by scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy, and X-ray powder diffraction (XRPD), and used for modification of glassy carbon paste electrode (GCPE). It was shown that introducing these nanoparticles to the structure of GCPE led to increasing analytical performance. Co ferrite modified GCPE (CoFeGCPE) showed better characteristics toward ascorbic acid sensing. The limit of detection (LOD) obtained by sensor was calculated to be 0.0270 mg/L, with linear range from 0.1758 to 2.6010 mg/L. This sensor was successfully applied for practical analysis, and the obtained results demonstrated that the proposed procedure could be a promising replacement for the conventional electrode materials and time-consuming and expensive separation methods. (C) 2016 Elsevier Inc. All rights reserved.
PB  - Academic Press Inc Elsevier Science, San Diego
T2  - Analytical Biochemistry
T1  - Amperometric ascorbic acid sensor based on doped ferrites nanoparticles modified glassy carbon paste electrode
VL  - 504
SP  - 20
EP  - 26
DO  - 10.1016/j.ab.2016.03.020
UR  - Kon_3069
ER  - 
@article{
author = "Dimitrijević, Teodora and Vulić, Predrag J. and Manojlović, Dragan D. and Nikolić, Aleksandar S. and Stanković, Dalibor",
year = "2016",
abstract = "In this study, a novel electrochemical sensor for quantification of ascorbic acid with amperometric detection in physiological conditions was constructed. For this purpose, cobalt and nickel ferrites were synthesized using microwave and ultrasound assistance, characterized by scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy, and X-ray powder diffraction (XRPD), and used for modification of glassy carbon paste electrode (GCPE). It was shown that introducing these nanoparticles to the structure of GCPE led to increasing analytical performance. Co ferrite modified GCPE (CoFeGCPE) showed better characteristics toward ascorbic acid sensing. The limit of detection (LOD) obtained by sensor was calculated to be 0.0270 mg/L, with linear range from 0.1758 to 2.6010 mg/L. This sensor was successfully applied for practical analysis, and the obtained results demonstrated that the proposed procedure could be a promising replacement for the conventional electrode materials and time-consuming and expensive separation methods. (C) 2016 Elsevier Inc. All rights reserved.",
publisher = "Academic Press Inc Elsevier Science, San Diego",
journal = "Analytical Biochemistry",
title = "Amperometric ascorbic acid sensor based on doped ferrites nanoparticles modified glassy carbon paste electrode",
volume = "504",
pages = "20-26",
doi = "10.1016/j.ab.2016.03.020",
url = "Kon_3069"
}
Dimitrijević, T., Vulić, P. J., Manojlović, D. D., Nikolić, A. S.,& Stanković, D.. (2016). Amperometric ascorbic acid sensor based on doped ferrites nanoparticles modified glassy carbon paste electrode. in Analytical Biochemistry
Academic Press Inc Elsevier Science, San Diego., 504, 20-26.
https://doi.org/10.1016/j.ab.2016.03.020
Kon_3069
Dimitrijević T, Vulić PJ, Manojlović DD, Nikolić AS, Stanković D. Amperometric ascorbic acid sensor based on doped ferrites nanoparticles modified glassy carbon paste electrode. in Analytical Biochemistry. 2016;504:20-26.
doi:10.1016/j.ab.2016.03.020
Kon_3069 .
Dimitrijević, Teodora, Vulić, Predrag J., Manojlović, Dragan D., Nikolić, Aleksandar S., Stanković, Dalibor, "Amperometric ascorbic acid sensor based on doped ferrites nanoparticles modified glassy carbon paste electrode" in Analytical Biochemistry, 504 (2016):20-26,
https://doi.org/10.1016/j.ab.2016.03.020 .,
Kon_3069 .
11
12
12

Supplementary data for the article: Dimitrijević, T.; Vulić, P.; Manojlović, D.; Nikolić, A. S.; Stanković, D. M. Amperometric Ascorbic Acid Sensor Based on Doped Ferrites Nanoparticles Modified Glassy Carbon Paste Electrode. Analytical Biochemistry 2016, 504, 20–26. https://doi.org/10.1016/j.ab.2016.03.020

Dimitrijević, Teodora; Vulić, Predrag J.; Manojlović, Dragan D.; Nikolić, Aleksandar S.; Stanković, Dalibor

(Academic Press Inc Elsevier Science, San Diego, 2016)

TY  - DATA
AU  - Dimitrijević, Teodora
AU  - Vulić, Predrag J.
AU  - Manojlović, Dragan D.
AU  - Nikolić, Aleksandar S.
AU  - Stanković, Dalibor
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3336
PB  - Academic Press Inc Elsevier Science, San Diego
T2  - Analytical Biochemistry
T1  - Supplementary data for the article: Dimitrijević, T.; Vulić, P.; Manojlović, D.; Nikolić, A. S.; Stanković, D. M. Amperometric Ascorbic Acid Sensor Based on Doped Ferrites Nanoparticles Modified Glassy Carbon Paste Electrode. Analytical Biochemistry 2016, 504, 20–26. https://doi.org/10.1016/j.ab.2016.03.020
ER  - 
@misc{
author = "Dimitrijević, Teodora and Vulić, Predrag J. and Manojlović, Dragan D. and Nikolić, Aleksandar S. and Stanković, Dalibor",
year = "2016",
publisher = "Academic Press Inc Elsevier Science, San Diego",
journal = "Analytical Biochemistry",
title = "Supplementary data for the article: Dimitrijević, T.; Vulić, P.; Manojlović, D.; Nikolić, A. S.; Stanković, D. M. Amperometric Ascorbic Acid Sensor Based on Doped Ferrites Nanoparticles Modified Glassy Carbon Paste Electrode. Analytical Biochemistry 2016, 504, 20–26. https://doi.org/10.1016/j.ab.2016.03.020"
}
Dimitrijević, T., Vulić, P. J., Manojlović, D. D., Nikolić, A. S.,& Stanković, D.. (2016). Supplementary data for the article: Dimitrijević, T.; Vulić, P.; Manojlović, D.; Nikolić, A. S.; Stanković, D. M. Amperometric Ascorbic Acid Sensor Based on Doped Ferrites Nanoparticles Modified Glassy Carbon Paste Electrode. Analytical Biochemistry 2016, 504, 20–26. https://doi.org/10.1016/j.ab.2016.03.020. in Analytical Biochemistry
Academic Press Inc Elsevier Science, San Diego..
Dimitrijević T, Vulić PJ, Manojlović DD, Nikolić AS, Stanković D. Supplementary data for the article: Dimitrijević, T.; Vulić, P.; Manojlović, D.; Nikolić, A. S.; Stanković, D. M. Amperometric Ascorbic Acid Sensor Based on Doped Ferrites Nanoparticles Modified Glassy Carbon Paste Electrode. Analytical Biochemistry 2016, 504, 20–26. https://doi.org/10.1016/j.ab.2016.03.020. in Analytical Biochemistry. 2016;..
Dimitrijević, Teodora, Vulić, Predrag J., Manojlović, Dragan D., Nikolić, Aleksandar S., Stanković, Dalibor, "Supplementary data for the article: Dimitrijević, T.; Vulić, P.; Manojlović, D.; Nikolić, A. S.; Stanković, D. M. Amperometric Ascorbic Acid Sensor Based on Doped Ferrites Nanoparticles Modified Glassy Carbon Paste Electrode. Analytical Biochemistry 2016, 504, 20–26. https://doi.org/10.1016/j.ab.2016.03.020" in Analytical Biochemistry (2016).

Sensitive Determination of Copper on New Modified Glassy Carbon Paste Electrode

Škrivanj, Sandra B.; Stanković, Dalibor; Khan, Muslim; Nikolić, Aleksandar S.; Vulić, Predrag J.; Manojlović, Dragan D.

(Univ Tehran, Fac Chemistry, Center Excellence Electrochemistry, Tehran, 2015)

TY  - JOUR
AU  - Škrivanj, Sandra B.
AU  - Stanković, Dalibor
AU  - Khan, Muslim
AU  - Nikolić, Aleksandar S.
AU  - Vulić, Predrag J.
AU  - Manojlović, Dragan D.
PY  - 2015
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2151
AB  - This paper describes determination of trace level of copper ions on a new type of modified glassy carbon paste electrode based on addition of different amount of Co-ferrites in glassy carbon paste (CoFeMGCPE). Co-ferrite nanoparticles with different amount of cobalt were synthesized and characterized using scanning electron microscopy (SEM) and X-ray powder diffraction (XRPD). A significant increase in current was achieved by introducing modifier in composition of the electrode in comparison with the bare glassy carbon paste electrode. Electrochemical parameters such as percentage of modifier, accumulation time and potential, pH and the optimized amount of cobalt in the ferrites were determined. The best voltammetric response was observed for Co0.5Fe0.5Fe2O4 when percentage of modifier was 3%. In acetate buffer solution, pH 4.5, thus prepared electrode displays selective detection toward copper ions, detection limit of 96 nM and it was successfully applied for the determination of copper ions in natural water samples, with satisfactory recovery.
PB  - Univ Tehran, Fac Chemistry, Center Excellence Electrochemistry, Tehran
T2  - Analytical and Bioanalytical Chemistry
T1  - Sensitive Determination of Copper on New Modified Glassy Carbon Paste Electrode
VL  - 7
IS  - 2
SP  - 230
EP  - 241
UR  - Kon_3482
ER  - 
@article{
author = "Škrivanj, Sandra B. and Stanković, Dalibor and Khan, Muslim and Nikolić, Aleksandar S. and Vulić, Predrag J. and Manojlović, Dragan D.",
year = "2015",
abstract = "This paper describes determination of trace level of copper ions on a new type of modified glassy carbon paste electrode based on addition of different amount of Co-ferrites in glassy carbon paste (CoFeMGCPE). Co-ferrite nanoparticles with different amount of cobalt were synthesized and characterized using scanning electron microscopy (SEM) and X-ray powder diffraction (XRPD). A significant increase in current was achieved by introducing modifier in composition of the electrode in comparison with the bare glassy carbon paste electrode. Electrochemical parameters such as percentage of modifier, accumulation time and potential, pH and the optimized amount of cobalt in the ferrites were determined. The best voltammetric response was observed for Co0.5Fe0.5Fe2O4 when percentage of modifier was 3%. In acetate buffer solution, pH 4.5, thus prepared electrode displays selective detection toward copper ions, detection limit of 96 nM and it was successfully applied for the determination of copper ions in natural water samples, with satisfactory recovery.",
publisher = "Univ Tehran, Fac Chemistry, Center Excellence Electrochemistry, Tehran",
journal = "Analytical and Bioanalytical Chemistry",
title = "Sensitive Determination of Copper on New Modified Glassy Carbon Paste Electrode",
volume = "7",
number = "2",
pages = "230-241",
url = "Kon_3482"
}
Škrivanj, S. B., Stanković, D., Khan, M., Nikolić, A. S., Vulić, P. J.,& Manojlović, D. D.. (2015). Sensitive Determination of Copper on New Modified Glassy Carbon Paste Electrode. in Analytical and Bioanalytical Chemistry
Univ Tehran, Fac Chemistry, Center Excellence Electrochemistry, Tehran., 7(2), 230-241.
Kon_3482
Škrivanj SB, Stanković D, Khan M, Nikolić AS, Vulić PJ, Manojlović DD. Sensitive Determination of Copper on New Modified Glassy Carbon Paste Electrode. in Analytical and Bioanalytical Chemistry. 2015;7(2):230-241.
Kon_3482 .
Škrivanj, Sandra B., Stanković, Dalibor, Khan, Muslim, Nikolić, Aleksandar S., Vulić, Predrag J., Manojlović, Dragan D., "Sensitive Determination of Copper on New Modified Glassy Carbon Paste Electrode" in Analytical and Bioanalytical Chemistry, 7, no. 2 (2015):230-241,
Kon_3482 .
4
3

Application of Novel Zn-Ferrite Modified Glassy Carbon Paste Electrode as a Sensor for Determination of Cd(II) in Waste Water

Stanković, Dalibor; Škrivanj, Sandra B.; Savić, Nenad; Nikolić, Aleksandar S.; Vulić, Predrag J.; Manojlović, Dragan D.

(Wiley-V C H Verlag Gmbh, Weinheim, 2014)

TY  - JOUR
AU  - Stanković, Dalibor
AU  - Škrivanj, Sandra B.
AU  - Savić, Nenad
AU  - Nikolić, Aleksandar S.
AU  - Vulić, Predrag J.
AU  - Manojlović, Dragan D.
PY  - 2014
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1821
AB  - This paper describes the preparation of a new sensor based on Zn-ferrite modified glassy carbon paste electrode and its electrochemical application for the determination of trace Cd(II) ions in waste waters using differential pulse anodic stripping voltammetry (DPASV). Different Zn/Ni ferrite nanoparticles were synthesized and characterized using scanning electron microscopy (SEM) and X-ray powder diffraction (XRPD). The prepared ferrite nanoparticles were used for the preparation of Zn-ferrite-modified glassy carbon paste electrode (ZnMGCPE) for determination of Cd(II) at nanomolar levels in waste water at pH 5. The different parameters such as conditions of preparation, Zn2+/Ni2+/Fe2+ ratio and electrochemical parameters, percentage of modifier, accumulation time, pH and accumulation potential were investigated. Besides, interference measurements were also evaluated under optimized parameters. The best voltammetric response was observed for ZnFe2O4 modifier, when the percentage of modifier was 3%, accumulation time 9 min, pH of supporting electrolyte 5 and accumulation potential -1.05 V. Thus prepared electrode displays excellent response to Cd(II) with a detection limit of 0.38 ppb, and selective detection toward Cd(II) was achieved.
PB  - Wiley-V C H Verlag Gmbh, Weinheim
T2  - Electroanalysis
T1  - Application of Novel Zn-Ferrite Modified Glassy Carbon Paste Electrode as a Sensor for Determination of Cd(II) in Waste Water
VL  - 26
IS  - 7
SP  - 1536
EP  - 1543
DO  - 10.1002/elan.201400095
UR  - Kon_2704
ER  - 
@article{
author = "Stanković, Dalibor and Škrivanj, Sandra B. and Savić, Nenad and Nikolić, Aleksandar S. and Vulić, Predrag J. and Manojlović, Dragan D.",
year = "2014",
abstract = "This paper describes the preparation of a new sensor based on Zn-ferrite modified glassy carbon paste electrode and its electrochemical application for the determination of trace Cd(II) ions in waste waters using differential pulse anodic stripping voltammetry (DPASV). Different Zn/Ni ferrite nanoparticles were synthesized and characterized using scanning electron microscopy (SEM) and X-ray powder diffraction (XRPD). The prepared ferrite nanoparticles were used for the preparation of Zn-ferrite-modified glassy carbon paste electrode (ZnMGCPE) for determination of Cd(II) at nanomolar levels in waste water at pH 5. The different parameters such as conditions of preparation, Zn2+/Ni2+/Fe2+ ratio and electrochemical parameters, percentage of modifier, accumulation time, pH and accumulation potential were investigated. Besides, interference measurements were also evaluated under optimized parameters. The best voltammetric response was observed for ZnFe2O4 modifier, when the percentage of modifier was 3%, accumulation time 9 min, pH of supporting electrolyte 5 and accumulation potential -1.05 V. Thus prepared electrode displays excellent response to Cd(II) with a detection limit of 0.38 ppb, and selective detection toward Cd(II) was achieved.",
publisher = "Wiley-V C H Verlag Gmbh, Weinheim",
journal = "Electroanalysis",
title = "Application of Novel Zn-Ferrite Modified Glassy Carbon Paste Electrode as a Sensor for Determination of Cd(II) in Waste Water",
volume = "26",
number = "7",
pages = "1536-1543",
doi = "10.1002/elan.201400095",
url = "Kon_2704"
}
Stanković, D., Škrivanj, S. B., Savić, N., Nikolić, A. S., Vulić, P. J.,& Manojlović, D. D.. (2014). Application of Novel Zn-Ferrite Modified Glassy Carbon Paste Electrode as a Sensor for Determination of Cd(II) in Waste Water. in Electroanalysis
Wiley-V C H Verlag Gmbh, Weinheim., 26(7), 1536-1543.
https://doi.org/10.1002/elan.201400095
Kon_2704
Stanković D, Škrivanj SB, Savić N, Nikolić AS, Vulić PJ, Manojlović DD. Application of Novel Zn-Ferrite Modified Glassy Carbon Paste Electrode as a Sensor for Determination of Cd(II) in Waste Water. in Electroanalysis. 2014;26(7):1536-1543.
doi:10.1002/elan.201400095
Kon_2704 .
Stanković, Dalibor, Škrivanj, Sandra B., Savić, Nenad, Nikolić, Aleksandar S., Vulić, Predrag J., Manojlović, Dragan D., "Application of Novel Zn-Ferrite Modified Glassy Carbon Paste Electrode as a Sensor for Determination of Cd(II) in Waste Water" in Electroanalysis, 26, no. 7 (2014):1536-1543,
https://doi.org/10.1002/elan.201400095 .,
Kon_2704 .
7
8
7

Fe Doped TiO2 Prepared by Microwave-Assisted Hydrothermal Process for Removal of As(III) and As(V) from Water

Anđelković, Ivan; Stanković, Dalibor; Nešić, Jelena; Krstic, Jugoslav; Vulić, Predrag J.; Manojlović, Dragan D.; Roglić, Goran

(Amer Chemical Soc, Washington, 2014)

TY  - JOUR
AU  - Anđelković, Ivan
AU  - Stanković, Dalibor
AU  - Nešić, Jelena
AU  - Krstic, Jugoslav
AU  - Vulić, Predrag J.
AU  - Manojlović, Dragan D.
AU  - Roglić, Goran
PY  - 2014
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1812
AB  - Elevated concentrations of arsenic in groundwater, which is used as a source for drinking water, is a worldwide problem. Use of TiO2 and iron doped TiO2 synthesized by a microwave-assisted hydrothermal method for As(III) and As(V) removal were examined. Synthesized sorbents were characterized with XRD and nitrogen physisorption. Synthesized sorbents have predominantly anatase structure, and no peaks for iron could be observed. Doping of iron increases the surface area of synthesized sorbents. Sorption experiments show that increase of iron in sorbents increases the sorption capacity for As(III) and As(V). Increase of pH from 3 to 11 has no influence on As(III) sorption but decreases the sorption of As(V). Batch isotherm studies were performed to determine the binding capacities of As(III) and As(V). As(III) followed the Freundlich isotherm model, while for As(V) a better fit was with the Langmuir isotherm. The results of competition of SO42- and PO43- anions on adsorption of As(III) indicated that both anions reduced substantially the efficiency of adsorption on both adsorbents while for As(V) only the presence of PO43- anion interfered with adsorption. Testing 10Fe/TiO2 sorbent with arsenic contaminated natural water showed that this material could be used for removal of arsenic to the level recommended by WHO without pretreatment.
PB  - Amer Chemical Soc, Washington
T2  - Industrial and Engineering Chemistry Research
T1  - Fe Doped TiO2 Prepared by Microwave-Assisted Hydrothermal Process for Removal of As(III) and As(V) from Water
VL  - 53
IS  - 27
SP  - 10841
EP  - 10848
DO  - 10.1021/ie500849r
UR  - Kon_2695
ER  - 
@article{
author = "Anđelković, Ivan and Stanković, Dalibor and Nešić, Jelena and Krstic, Jugoslav and Vulić, Predrag J. and Manojlović, Dragan D. and Roglić, Goran",
year = "2014",
abstract = "Elevated concentrations of arsenic in groundwater, which is used as a source for drinking water, is a worldwide problem. Use of TiO2 and iron doped TiO2 synthesized by a microwave-assisted hydrothermal method for As(III) and As(V) removal were examined. Synthesized sorbents were characterized with XRD and nitrogen physisorption. Synthesized sorbents have predominantly anatase structure, and no peaks for iron could be observed. Doping of iron increases the surface area of synthesized sorbents. Sorption experiments show that increase of iron in sorbents increases the sorption capacity for As(III) and As(V). Increase of pH from 3 to 11 has no influence on As(III) sorption but decreases the sorption of As(V). Batch isotherm studies were performed to determine the binding capacities of As(III) and As(V). As(III) followed the Freundlich isotherm model, while for As(V) a better fit was with the Langmuir isotherm. The results of competition of SO42- and PO43- anions on adsorption of As(III) indicated that both anions reduced substantially the efficiency of adsorption on both adsorbents while for As(V) only the presence of PO43- anion interfered with adsorption. Testing 10Fe/TiO2 sorbent with arsenic contaminated natural water showed that this material could be used for removal of arsenic to the level recommended by WHO without pretreatment.",
publisher = "Amer Chemical Soc, Washington",
journal = "Industrial and Engineering Chemistry Research",
title = "Fe Doped TiO2 Prepared by Microwave-Assisted Hydrothermal Process for Removal of As(III) and As(V) from Water",
volume = "53",
number = "27",
pages = "10841-10848",
doi = "10.1021/ie500849r",
url = "Kon_2695"
}
Anđelković, I., Stanković, D., Nešić, J., Krstic, J., Vulić, P. J., Manojlović, D. D.,& Roglić, G.. (2014). Fe Doped TiO2 Prepared by Microwave-Assisted Hydrothermal Process for Removal of As(III) and As(V) from Water. in Industrial and Engineering Chemistry Research
Amer Chemical Soc, Washington., 53(27), 10841-10848.
https://doi.org/10.1021/ie500849r
Kon_2695
Anđelković I, Stanković D, Nešić J, Krstic J, Vulić PJ, Manojlović DD, Roglić G. Fe Doped TiO2 Prepared by Microwave-Assisted Hydrothermal Process for Removal of As(III) and As(V) from Water. in Industrial and Engineering Chemistry Research. 2014;53(27):10841-10848.
doi:10.1021/ie500849r
Kon_2695 .
Anđelković, Ivan, Stanković, Dalibor, Nešić, Jelena, Krstic, Jugoslav, Vulić, Predrag J., Manojlović, Dragan D., Roglić, Goran, "Fe Doped TiO2 Prepared by Microwave-Assisted Hydrothermal Process for Removal of As(III) and As(V) from Water" in Industrial and Engineering Chemistry Research, 53, no. 27 (2014):10841-10848,
https://doi.org/10.1021/ie500849r .,
Kon_2695 .
27
27
26

Fenton-like oxidation of an azo dye using mesoporous Fe/TiO2 catalysts prepared by a microwave-assisted hydrothermal process

Nešić, Jelena; Manojlović, Dragan D.; Jović, Milica; Dojčinović, Biljana P.; Vulić, Predrag J.; Krstic, Jugoslav; Roglić, Goran

(Serbian Chemical Soc, Belgrade, 2014)

TY  - JOUR
AU  - Nešić, Jelena
AU  - Manojlović, Dragan D.
AU  - Jović, Milica
AU  - Dojčinović, Biljana P.
AU  - Vulić, Predrag J.
AU  - Krstic, Jugoslav
AU  - Roglić, Goran
PY  - 2014
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1835
AB  - Fe-doped TiO2 photocatalysts with different contents of Fe (0.5, 1.6, 3.4 and 6.4 %) were synthesized by a microwave-hydrothermal method and characterized by X-ray diffraction analysis, N-2 physisorption at 77 K and UV-Vis spectrometry. The characterization showed that the Fe ions were highly dispersed in the TiO2 lattice. It was found that all the synthesized catalysts had a mesoporous structure and that Fe-doping increased the BET surface area. The UV-Vis study showed that the absorption spectra were shifted to longer wavelengths (red shift) with increasing dopant concentration. The photocatalytic activity of the samples was evaluated by the decolorization of the textile dye Reactive Blue 52 (RB) in aqueous solutions under sun-like radiation in the presence of H2O2 (a heterogeneous photo-Fenton process). The photocatalyst with 3.4 % Fe was found to be the most efficient in the presence of H2O2. The effect of the initial pH of the dye solution was assessed and dissolution of iron ions was studied as a function of pH value. It was concluded that decolorization was more favorable in acidic pH, and that at pH values  gt 4, the release of Fe ions into the solution was negligible. Photocatalytic degradation of 4-chlorophenol (4-CP) was investigated under the optimal conditions and it was shown that the catalyst was capable of degrading colorless pollutants.
PB  - Serbian Chemical Soc, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Fenton-like oxidation of an azo dye using mesoporous Fe/TiO2 catalysts prepared by a microwave-assisted hydrothermal process
VL  - 79
IS  - 8
SP  - 977
EP  - 991
DO  - 10.2298/JSC131001143N
UR  - Kon_2718
ER  - 
@article{
author = "Nešić, Jelena and Manojlović, Dragan D. and Jović, Milica and Dojčinović, Biljana P. and Vulić, Predrag J. and Krstic, Jugoslav and Roglić, Goran",
year = "2014",
abstract = "Fe-doped TiO2 photocatalysts with different contents of Fe (0.5, 1.6, 3.4 and 6.4 %) were synthesized by a microwave-hydrothermal method and characterized by X-ray diffraction analysis, N-2 physisorption at 77 K and UV-Vis spectrometry. The characterization showed that the Fe ions were highly dispersed in the TiO2 lattice. It was found that all the synthesized catalysts had a mesoporous structure and that Fe-doping increased the BET surface area. The UV-Vis study showed that the absorption spectra were shifted to longer wavelengths (red shift) with increasing dopant concentration. The photocatalytic activity of the samples was evaluated by the decolorization of the textile dye Reactive Blue 52 (RB) in aqueous solutions under sun-like radiation in the presence of H2O2 (a heterogeneous photo-Fenton process). The photocatalyst with 3.4 % Fe was found to be the most efficient in the presence of H2O2. The effect of the initial pH of the dye solution was assessed and dissolution of iron ions was studied as a function of pH value. It was concluded that decolorization was more favorable in acidic pH, and that at pH values  gt 4, the release of Fe ions into the solution was negligible. Photocatalytic degradation of 4-chlorophenol (4-CP) was investigated under the optimal conditions and it was shown that the catalyst was capable of degrading colorless pollutants.",
publisher = "Serbian Chemical Soc, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Fenton-like oxidation of an azo dye using mesoporous Fe/TiO2 catalysts prepared by a microwave-assisted hydrothermal process",
volume = "79",
number = "8",
pages = "977-991",
doi = "10.2298/JSC131001143N",
url = "Kon_2718"
}
Nešić, J., Manojlović, D. D., Jović, M., Dojčinović, B. P., Vulić, P. J., Krstic, J.,& Roglić, G.. (2014). Fenton-like oxidation of an azo dye using mesoporous Fe/TiO2 catalysts prepared by a microwave-assisted hydrothermal process. in Journal of the Serbian Chemical Society
Serbian Chemical Soc, Belgrade., 79(8), 977-991.
https://doi.org/10.2298/JSC131001143N
Kon_2718
Nešić J, Manojlović DD, Jović M, Dojčinović BP, Vulić PJ, Krstic J, Roglić G. Fenton-like oxidation of an azo dye using mesoporous Fe/TiO2 catalysts prepared by a microwave-assisted hydrothermal process. in Journal of the Serbian Chemical Society. 2014;79(8):977-991.
doi:10.2298/JSC131001143N
Kon_2718 .
Nešić, Jelena, Manojlović, Dragan D., Jović, Milica, Dojčinović, Biljana P., Vulić, Predrag J., Krstic, Jugoslav, Roglić, Goran, "Fenton-like oxidation of an azo dye using mesoporous Fe/TiO2 catalysts prepared by a microwave-assisted hydrothermal process" in Journal of the Serbian Chemical Society, 79, no. 8 (2014):977-991,
https://doi.org/10.2298/JSC131001143N .,
Kon_2718 .
10
10
10

Preparation, characterization and photocatalytic activity of lanthanum and vanadium co-doped mesoporous TiO2 for azo-dye degradation

Nešić, Jelena; Manojlović, Dragan D.; Anđelković, Ivan; Dojčinović, Biljana P.; Vulić, Predrag J.; Krstic, Jugoslav; Roglić, Goran

(Elsevier Science Bv, Amsterdam, 2013)

TY  - JOUR
AU  - Nešić, Jelena
AU  - Manojlović, Dragan D.
AU  - Anđelković, Ivan
AU  - Dojčinović, Biljana P.
AU  - Vulić, Predrag J.
AU  - Krstic, Jugoslav
AU  - Roglić, Goran
PY  - 2013
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3514
AB  - Titanium dioxide photocatalysts co-doped with lanthanum and vanadium were prepared by a facile microwave-assisted hydrothermal method and characterized by XRD, SEM, N-2 physisorption at 77 K and DRS. The characterization showed that co-doped TiO2 samples have a high degree of crystallinity and existence of fully anatase phase. It was found that all the synthesized catalysts have the mesoporous structure. The co-doped TiO2 samples have larger BET surface areas and the mesopores volume than pure TiO2 and La doped samples. The vanadium co-doping contributes to the extension of absorption into the visible region. The photocatalytic activity of the samples was evaluated by the decolorization of textile dye Reactive Blue 52 in aqueous solutions under sun-like radiation. Compared with La singly doped TiO2, the co-doped catalysts showed an important improvement of photoactivity. The photocatalyst with 2% (w/w) La and 0.02% (w/w) V appeared to be the most photoactive. Optimal catalyst loading and the kinetics of degradation were also studied. Demonstrating higher photodegradation efficiency for RB than commercially available TiO2 Evonik P25, easy separation from suspension by spontaneous sedimentation and reusability of the catalyst, make this photocatalyst suitable for wastewater treatment.
PB  - Elsevier Science Bv, Amsterdam
T2  - Journal of Molecular Catalysis. A: Chemical
T1  - Preparation, characterization and photocatalytic activity of lanthanum and vanadium co-doped mesoporous TiO2 for azo-dye degradation
VL  - 378
SP  - 67
EP  - 75
DO  - 10.1016/j.molcata.2013.05.018
ER  - 
@article{
author = "Nešić, Jelena and Manojlović, Dragan D. and Anđelković, Ivan and Dojčinović, Biljana P. and Vulić, Predrag J. and Krstic, Jugoslav and Roglić, Goran",
year = "2013",
abstract = "Titanium dioxide photocatalysts co-doped with lanthanum and vanadium were prepared by a facile microwave-assisted hydrothermal method and characterized by XRD, SEM, N-2 physisorption at 77 K and DRS. The characterization showed that co-doped TiO2 samples have a high degree of crystallinity and existence of fully anatase phase. It was found that all the synthesized catalysts have the mesoporous structure. The co-doped TiO2 samples have larger BET surface areas and the mesopores volume than pure TiO2 and La doped samples. The vanadium co-doping contributes to the extension of absorption into the visible region. The photocatalytic activity of the samples was evaluated by the decolorization of textile dye Reactive Blue 52 in aqueous solutions under sun-like radiation. Compared with La singly doped TiO2, the co-doped catalysts showed an important improvement of photoactivity. The photocatalyst with 2% (w/w) La and 0.02% (w/w) V appeared to be the most photoactive. Optimal catalyst loading and the kinetics of degradation were also studied. Demonstrating higher photodegradation efficiency for RB than commercially available TiO2 Evonik P25, easy separation from suspension by spontaneous sedimentation and reusability of the catalyst, make this photocatalyst suitable for wastewater treatment.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Journal of Molecular Catalysis. A: Chemical",
title = "Preparation, characterization and photocatalytic activity of lanthanum and vanadium co-doped mesoporous TiO2 for azo-dye degradation",
volume = "378",
pages = "67-75",
doi = "10.1016/j.molcata.2013.05.018"
}
Nešić, J., Manojlović, D. D., Anđelković, I., Dojčinović, B. P., Vulić, P. J., Krstic, J.,& Roglić, G.. (2013). Preparation, characterization and photocatalytic activity of lanthanum and vanadium co-doped mesoporous TiO2 for azo-dye degradation. in Journal of Molecular Catalysis. A: Chemical
Elsevier Science Bv, Amsterdam., 378, 67-75.
https://doi.org/10.1016/j.molcata.2013.05.018
Nešić J, Manojlović DD, Anđelković I, Dojčinović BP, Vulić PJ, Krstic J, Roglić G. Preparation, characterization and photocatalytic activity of lanthanum and vanadium co-doped mesoporous TiO2 for azo-dye degradation. in Journal of Molecular Catalysis. A: Chemical. 2013;378:67-75.
doi:10.1016/j.molcata.2013.05.018 .
Nešić, Jelena, Manojlović, Dragan D., Anđelković, Ivan, Dojčinović, Biljana P., Vulić, Predrag J., Krstic, Jugoslav, Roglić, Goran, "Preparation, characterization and photocatalytic activity of lanthanum and vanadium co-doped mesoporous TiO2 for azo-dye degradation" in Journal of Molecular Catalysis. A: Chemical, 378 (2013):67-75,
https://doi.org/10.1016/j.molcata.2013.05.018 . .
33
30
30

Preparation, characterization and photocatalytic activity of lanthanum and vanadium co-doped mesoporous TiO2 for azo-dye degradation

Nešić, Jelena; Manojlović, Dragan D.; Anđelković, Ivan; Dojčinović, Biljana P.; Vulić, Predrag J.; Krstic, Jugoslav; Roglić, Goran

(Elsevier Science Bv, Amsterdam, 2013)

TY  - JOUR
AU  - Nešić, Jelena
AU  - Manojlović, Dragan D.
AU  - Anđelković, Ivan
AU  - Dojčinović, Biljana P.
AU  - Vulić, Predrag J.
AU  - Krstic, Jugoslav
AU  - Roglić, Goran
PY  - 2013
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1405
AB  - Titanium dioxide photocatalysts co-doped with lanthanum and vanadium were prepared by a facile microwave-assisted hydrothermal method and characterized by XRD, SEM, N-2 physisorption at 77 K and DRS. The characterization showed that co-doped TiO2 samples have a high degree of crystallinity and existence of fully anatase phase. It was found that all the synthesized catalysts have the mesoporous structure. The co-doped TiO2 samples have larger BET surface areas and the mesopores volume than pure TiO2 and La doped samples. The vanadium co-doping contributes to the extension of absorption into the visible region. The photocatalytic activity of the samples was evaluated by the decolorization of textile dye Reactive Blue 52 in aqueous solutions under sun-like radiation. Compared with La singly doped TiO2, the co-doped catalysts showed an important improvement of photoactivity. The photocatalyst with 2% (w/w) La and 0.02% (w/w) V appeared to be the most photoactive. Optimal catalyst loading and the kinetics of degradation were also studied. Demonstrating higher photodegradation efficiency for RB than commercially available TiO2 Evonik P25, easy separation from suspension by spontaneous sedimentation and reusability of the catalyst, make this photocatalyst suitable for wastewater treatment.
PB  - Elsevier Science Bv, Amsterdam
T2  - Journal of Molecular Catalysis. A: Chemical
T1  - Preparation, characterization and photocatalytic activity of lanthanum and vanadium co-doped mesoporous TiO2 for azo-dye degradation
VL  - 378
SP  - 67
EP  - 75
DO  - 10.1016/j.molcata.2013.05.018
UR  - Kon_2525
ER  - 
@article{
author = "Nešić, Jelena and Manojlović, Dragan D. and Anđelković, Ivan and Dojčinović, Biljana P. and Vulić, Predrag J. and Krstic, Jugoslav and Roglić, Goran",
year = "2013",
abstract = "Titanium dioxide photocatalysts co-doped with lanthanum and vanadium were prepared by a facile microwave-assisted hydrothermal method and characterized by XRD, SEM, N-2 physisorption at 77 K and DRS. The characterization showed that co-doped TiO2 samples have a high degree of crystallinity and existence of fully anatase phase. It was found that all the synthesized catalysts have the mesoporous structure. The co-doped TiO2 samples have larger BET surface areas and the mesopores volume than pure TiO2 and La doped samples. The vanadium co-doping contributes to the extension of absorption into the visible region. The photocatalytic activity of the samples was evaluated by the decolorization of textile dye Reactive Blue 52 in aqueous solutions under sun-like radiation. Compared with La singly doped TiO2, the co-doped catalysts showed an important improvement of photoactivity. The photocatalyst with 2% (w/w) La and 0.02% (w/w) V appeared to be the most photoactive. Optimal catalyst loading and the kinetics of degradation were also studied. Demonstrating higher photodegradation efficiency for RB than commercially available TiO2 Evonik P25, easy separation from suspension by spontaneous sedimentation and reusability of the catalyst, make this photocatalyst suitable for wastewater treatment.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Journal of Molecular Catalysis. A: Chemical",
title = "Preparation, characterization and photocatalytic activity of lanthanum and vanadium co-doped mesoporous TiO2 for azo-dye degradation",
volume = "378",
pages = "67-75",
doi = "10.1016/j.molcata.2013.05.018",
url = "Kon_2525"
}
Nešić, J., Manojlović, D. D., Anđelković, I., Dojčinović, B. P., Vulić, P. J., Krstic, J.,& Roglić, G.. (2013). Preparation, characterization and photocatalytic activity of lanthanum and vanadium co-doped mesoporous TiO2 for azo-dye degradation. in Journal of Molecular Catalysis. A: Chemical
Elsevier Science Bv, Amsterdam., 378, 67-75.
https://doi.org/10.1016/j.molcata.2013.05.018
Kon_2525
Nešić J, Manojlović DD, Anđelković I, Dojčinović BP, Vulić PJ, Krstic J, Roglić G. Preparation, characterization and photocatalytic activity of lanthanum and vanadium co-doped mesoporous TiO2 for azo-dye degradation. in Journal of Molecular Catalysis. A: Chemical. 2013;378:67-75.
doi:10.1016/j.molcata.2013.05.018
Kon_2525 .
Nešić, Jelena, Manojlović, Dragan D., Anđelković, Ivan, Dojčinović, Biljana P., Vulić, Predrag J., Krstic, Jugoslav, Roglić, Goran, "Preparation, characterization and photocatalytic activity of lanthanum and vanadium co-doped mesoporous TiO2 for azo-dye degradation" in Journal of Molecular Catalysis. A: Chemical, 378 (2013):67-75,
https://doi.org/10.1016/j.molcata.2013.05.018 .,
Kon_2525 .
33
30
31

Aerosol synthesis of pure and Pt-doped ZnO particles using nitrate and pdda-Pt(IV) complex solutions

Djinovic, VM; Mancic, LT; Bogdanović, Goran A.; Vulić, Predrag J.; del Rosario, G; Sabo, Tibor; Milošević, Olivera B.

(Cambridge Univ Press, New York, 2005)

TY  - JOUR
AU  - Djinovic, VM
AU  - Mancic, LT
AU  - Bogdanović, Goran A.
AU  - Vulić, Predrag J.
AU  - del Rosario, G
AU  - Sabo, Tibor
AU  - Milošević, Olivera B.
PY  - 2005
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/703
AB  - Pure and Pt-doped ZnO nanophase particles were synthesized by ultrasonic spray pyrolysis. The particles were obtained through the decomposition of zinc nitrate and with a newly developed Pt(IV) complex with 1,3 -propylenediamine-NN'-diacetate tetradentate class ligand (pdda). The complex was characterized by elemental analysis, electronic absorption and infrared spectroscopy. The form of the determined complex structure {trans-[Pt(pdda)Br-2]center dot H2O} implies that Pt(IV) ion has a distorted octahedral coordination due to intramolecular N-H center dot center dot center dot Br interaction. The results of structural refinement (cell parameters, bond lengths, and ion occupancy) of ultrasonically derived pure and Pt-doped ZnO particles suggest either the formation of Zn-i interstitials or platinum ion incorporation into the ZnO lattice in octahedral interstitial positions, respectively. A well-crystallized hexagonal wurtzite structure of ZnO was pronounced in all investigated samples [JCPDS card 36-1415, Joint Committee on Powder Diffraction Standards, defined by International Centre for Diffraction Data (www.icdd.com)]. Phase determination also indicated the presence of a nitrate hydroxide hydrate phase (JCPDS card 24-1460), as a result of incomplete precursor decomposition and a spinel Zn2PtO4 phase (below 1.0 wt%) located in the boundary region for a Pt-doped ZnO sample. Based on x-ray diffraction, scanning electron microscopy, and energy-dispersive spectroscopy analyses, it was shown that the different particle growing morphologies, which were either spheroidally or pyramidally shaped, were influenced by the precursor chemistry, processing parameters and the presence of platinum ions. The composite internal particle structure revealed by transmission electron microscopy and selected area electron diffraction analyses, implied that the secondary particles represent an assembly of primary particles sized under 60 nm aroused during the processes of nucleation, growth and aggregation. Both hexagonal and spheroidal shape of primary particles was evident. The particle morphology, primarily particle size and the mechanism of Pt4+ ion introduction into the ZnO cell was discussed based on the structural refinement and selected area electron diffraction analysis.
PB  - Cambridge Univ Press, New York
T2  - Journal of Materials Research
T1  - Aerosol synthesis of pure and Pt-doped ZnO particles using nitrate and pdda-Pt(IV) complex solutions
VL  - 20
IS  - 1
SP  - 102
EP  - 113
DO  - 10.1557/JMR.2005.0006
UR  - Kon_1656
ER  - 
@article{
author = "Djinovic, VM and Mancic, LT and Bogdanović, Goran A. and Vulić, Predrag J. and del Rosario, G and Sabo, Tibor and Milošević, Olivera B.",
year = "2005",
abstract = "Pure and Pt-doped ZnO nanophase particles were synthesized by ultrasonic spray pyrolysis. The particles were obtained through the decomposition of zinc nitrate and with a newly developed Pt(IV) complex with 1,3 -propylenediamine-NN'-diacetate tetradentate class ligand (pdda). The complex was characterized by elemental analysis, electronic absorption and infrared spectroscopy. The form of the determined complex structure {trans-[Pt(pdda)Br-2]center dot H2O} implies that Pt(IV) ion has a distorted octahedral coordination due to intramolecular N-H center dot center dot center dot Br interaction. The results of structural refinement (cell parameters, bond lengths, and ion occupancy) of ultrasonically derived pure and Pt-doped ZnO particles suggest either the formation of Zn-i interstitials or platinum ion incorporation into the ZnO lattice in octahedral interstitial positions, respectively. A well-crystallized hexagonal wurtzite structure of ZnO was pronounced in all investigated samples [JCPDS card 36-1415, Joint Committee on Powder Diffraction Standards, defined by International Centre for Diffraction Data (www.icdd.com)]. Phase determination also indicated the presence of a nitrate hydroxide hydrate phase (JCPDS card 24-1460), as a result of incomplete precursor decomposition and a spinel Zn2PtO4 phase (below 1.0 wt%) located in the boundary region for a Pt-doped ZnO sample. Based on x-ray diffraction, scanning electron microscopy, and energy-dispersive spectroscopy analyses, it was shown that the different particle growing morphologies, which were either spheroidally or pyramidally shaped, were influenced by the precursor chemistry, processing parameters and the presence of platinum ions. The composite internal particle structure revealed by transmission electron microscopy and selected area electron diffraction analyses, implied that the secondary particles represent an assembly of primary particles sized under 60 nm aroused during the processes of nucleation, growth and aggregation. Both hexagonal and spheroidal shape of primary particles was evident. The particle morphology, primarily particle size and the mechanism of Pt4+ ion introduction into the ZnO cell was discussed based on the structural refinement and selected area electron diffraction analysis.",
publisher = "Cambridge Univ Press, New York",
journal = "Journal of Materials Research",
title = "Aerosol synthesis of pure and Pt-doped ZnO particles using nitrate and pdda-Pt(IV) complex solutions",
volume = "20",
number = "1",
pages = "102-113",
doi = "10.1557/JMR.2005.0006",
url = "Kon_1656"
}
Djinovic, V., Mancic, L., Bogdanović, G. A., Vulić, P. J., del Rosario, G., Sabo, T.,& Milošević, O. B.. (2005). Aerosol synthesis of pure and Pt-doped ZnO particles using nitrate and pdda-Pt(IV) complex solutions. in Journal of Materials Research
Cambridge Univ Press, New York., 20(1), 102-113.
https://doi.org/10.1557/JMR.2005.0006
Kon_1656
Djinovic V, Mancic L, Bogdanović GA, Vulić PJ, del Rosario G, Sabo T, Milošević OB. Aerosol synthesis of pure and Pt-doped ZnO particles using nitrate and pdda-Pt(IV) complex solutions. in Journal of Materials Research. 2005;20(1):102-113.
doi:10.1557/JMR.2005.0006
Kon_1656 .
Djinovic, VM, Mancic, LT, Bogdanović, Goran A., Vulić, Predrag J., del Rosario, G, Sabo, Tibor, Milošević, Olivera B., "Aerosol synthesis of pure and Pt-doped ZnO particles using nitrate and pdda-Pt(IV) complex solutions" in Journal of Materials Research, 20, no. 1 (2005):102-113,
https://doi.org/10.1557/JMR.2005.0006 .,
Kon_1656 .
3
9
8
10