TY  - JOUR
AU  - Milošević, Ksenija
AU  - Lončarević, Davor
AU  - Mudrinić, Tihana
AU  - Kalagasidis Krušić, Melina
AU  - Dostanić, Jasmina
PY  - 2023
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5803
AB  - The visible-light-active heterojunctions based on TiO2 were extensively investigated due to their wide range of energy and environment applications. In this study, g-C3N4/titanate heterojunction photocatalyst was successfully prepared by a simple one-step calcination route from melamine and hydrothermally prepared titanates. The photocatalyst was characterized by different physicochemical methods, e.g., X-ray diffraction (XRD), scanning electron microscopy (SEM), and N2 physisorption analysis. The photocatalytic efficiency of synthesized photocatalyst was evaluated by single and simultaneous degradation of methylene blue (MB) and orange G (OG) dyes under solar and visible light irradiation. The photocatalyst exhibited improved visible light activity due to the efficient separation of photogenerated charge carriers and enhanced visible light absorption. The degradation of MB was examined under different reaction conditions to assess the influence of initial MB concentration, catalyst loading, and pH on the degradation kinetics. Dye degradation study in the single and binary dye systems revealed that adsorption was limiting step that governs the pollutant degradation order. Radical trapping experiments were performed using different types of scavengers to highlight the difference in photochemical reactions and mechanism of MB and OG dye degradation under different light irradiation. Comparison of the reaction pathways under visible and solar light irradiation supported with determined bandgap edges and photoluminescence (PL) analysis suggested that the g-C3N4/titanate heterojunction belonged to the type II heterojunction.
PB  - Springer Science and Business Media B.V.
T2  - Journal of Nanoparticle Research
T1  - Mechanistic insights into the simultaneous visible-light induced photodegradation of organic pollutants by g-C3N4/titanate heterojunction
IS  - 2
SP  - 26
VL  - 25
DO  - 10.1007/s11051-023-05673-x
ER  - 

@article{
author = "Milošević, Ksenija and Lončarević, Davor and Mudrinić, Tihana and Kalagasidis Krušić, Melina and Dostanić, Jasmina",
year = "2023",
abstract = "The visible-light-active heterojunctions based on TiO2 were extensively investigated due to their wide range of energy and environment applications. In this study, g-C3N4/titanate heterojunction photocatalyst was successfully prepared by a simple one-step calcination route from melamine and hydrothermally prepared titanates. The photocatalyst was characterized by different physicochemical methods, e.g., X-ray diffraction (XRD), scanning electron microscopy (SEM), and N2 physisorption analysis. The photocatalytic efficiency of synthesized photocatalyst was evaluated by single and simultaneous degradation of methylene blue (MB) and orange G (OG) dyes under solar and visible light irradiation. The photocatalyst exhibited improved visible light activity due to the efficient separation of photogenerated charge carriers and enhanced visible light absorption. The degradation of MB was examined under different reaction conditions to assess the influence of initial MB concentration, catalyst loading, and pH on the degradation kinetics. Dye degradation study in the single and binary dye systems revealed that adsorption was limiting step that governs the pollutant degradation order. Radical trapping experiments were performed using different types of scavengers to highlight the difference in photochemical reactions and mechanism of MB and OG dye degradation under different light irradiation. Comparison of the reaction pathways under visible and solar light irradiation supported with determined bandgap edges and photoluminescence (PL) analysis suggested that the g-C3N4/titanate heterojunction belonged to the type II heterojunction.",
publisher = "Springer Science and Business Media B.V.",
journal = "Journal of Nanoparticle Research",
title = "Mechanistic insights into the simultaneous visible-light induced photodegradation of organic pollutants by g-C3N4/titanate heterojunction",
number = "2",
pages = "26",
volume = "25",
doi = "10.1007/s11051-023-05673-x"
}

Milošević, K., Lončarević, D., Mudrinić, T., Kalagasidis Krušić, M.,& Dostanić, J.. (2023). Mechanistic insights into the simultaneous visible-light induced photodegradation of organic pollutants by g-C3N4/titanate heterojunction. in Journal of Nanoparticle Research
Springer Science and Business Media B.V.., 25(2), 26.
https://doi.org/10.1007/s11051-023-05673-x

Milošević K, Lončarević D, Mudrinić T, Kalagasidis Krušić M, Dostanić J. Mechanistic insights into the simultaneous visible-light induced photodegradation of organic pollutants by g-C3N4/titanate heterojunction. in Journal of Nanoparticle Research. 2023;25(2):26.
doi:10.1007/s11051-023-05673-x .

Milošević, Ksenija, Lončarević, Davor, Mudrinić, Tihana, Kalagasidis Krušić, Melina, Dostanić, Jasmina, "Mechanistic insights into the simultaneous visible-light induced photodegradation of organic pollutants by g-C3N4/titanate heterojunction" in Journal of Nanoparticle Research, 25, no. 2 (2023):26,
https://doi.org/10.1007/s11051-023-05673-x . .

TY  - JOUR
AU  - Pavlović, Stefan
AU  - Marinković, Dalibor
AU  - Kostić, Milan
AU  - Lončarević, Davor
AU  - Mojović, Ljiljana
AU  - Stanković, Miroslav
AU  - Veljković, Vlada B.
PY  - 2021
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4586
AB  - Lignite coal fly ash (FA) from a domestic thermal power plant was converted into a pure cancrinite zeolitic material (ZMFA) using a novel, custom-made, rotating autoclave reactor system by a short-term alkali activation process. The obtained ZMFA was used as catalyst support of calcium oxide as an active component derived from waste chicken eggshells (ES). The ZMFA supported calcium oxide catalyst (xCaO/ZMFA) was synthesized by means of the ultrasound-assisted method. The influence of different concentrations of dispersed calcium oxide (x = 5–20 wt%) over ZMFA and thermal treatment at different temperatures (450–600 °C) were studied. The structural and morphological characterization showed that the original cancrinite structure was preserved. The basicity and textural properties indicated the presence of strong active sites in a well-defined pore network suitable for the reactions of bulky organic compounds such as triacylglycerols (TAGs). The highest activity (96.5% of fatty acid methyl esters) in the methanolysis of sunflower oil was achieved with the 20CaO/ZMFA catalyst under reaction conditions: temperature of 60 °C, methanol/oil molar ratio of 12:1, catalyst concentration of 4 wt%, and reaction time of 2 h. It was found that the optimal calcination temperature of the catalyst precursor was 550 °C. At calcination temperatures above 550 °C, the melting of the glassy phase became more intense whereby the molten phase partially reacted with calcium oxide forming the catalytically inactive calcium silicate compounds (wollastonite, larnite, etc.). The rate constants of the two tested kinetic models were correlated with the concentrations of active calcium oxide. The MRPD of both models was low indicating their reliability.
PB  - Elsevier
T2  - Fuel
T1  - The chicken eggshell calcium oxide ultrasonically dispersed over lignite coal fly ash-based cancrinite zeolite support as a catalyst for biodiesel production
SP  - 119912
VL  - 289
DO  - 10.1016/j.fuel.2020.119912
ER  - 

@article{
author = "Pavlović, Stefan and Marinković, Dalibor and Kostić, Milan and Lončarević, Davor and Mojović, Ljiljana and Stanković, Miroslav and Veljković, Vlada B.",
year = "2021",
abstract = "Lignite coal fly ash (FA) from a domestic thermal power plant was converted into a pure cancrinite zeolitic material (ZMFA) using a novel, custom-made, rotating autoclave reactor system by a short-term alkali activation process. The obtained ZMFA was used as catalyst support of calcium oxide as an active component derived from waste chicken eggshells (ES). The ZMFA supported calcium oxide catalyst (xCaO/ZMFA) was synthesized by means of the ultrasound-assisted method. The influence of different concentrations of dispersed calcium oxide (x = 5–20 wt%) over ZMFA and thermal treatment at different temperatures (450–600 °C) were studied. The structural and morphological characterization showed that the original cancrinite structure was preserved. The basicity and textural properties indicated the presence of strong active sites in a well-defined pore network suitable for the reactions of bulky organic compounds such as triacylglycerols (TAGs). The highest activity (96.5% of fatty acid methyl esters) in the methanolysis of sunflower oil was achieved with the 20CaO/ZMFA catalyst under reaction conditions: temperature of 60 °C, methanol/oil molar ratio of 12:1, catalyst concentration of 4 wt%, and reaction time of 2 h. It was found that the optimal calcination temperature of the catalyst precursor was 550 °C. At calcination temperatures above 550 °C, the melting of the glassy phase became more intense whereby the molten phase partially reacted with calcium oxide forming the catalytically inactive calcium silicate compounds (wollastonite, larnite, etc.). The rate constants of the two tested kinetic models were correlated with the concentrations of active calcium oxide. The MRPD of both models was low indicating their reliability.",
publisher = "Elsevier",
journal = "Fuel",
title = "The chicken eggshell calcium oxide ultrasonically dispersed over lignite coal fly ash-based cancrinite zeolite support as a catalyst for biodiesel production",
pages = "119912",
volume = "289",
doi = "10.1016/j.fuel.2020.119912"
}

Pavlović, S., Marinković, D., Kostić, M., Lončarević, D., Mojović, L., Stanković, M.,& Veljković, V. B.. (2021). The chicken eggshell calcium oxide ultrasonically dispersed over lignite coal fly ash-based cancrinite zeolite support as a catalyst for biodiesel production. in Fuel
Elsevier., 289, 119912.
https://doi.org/10.1016/j.fuel.2020.119912

Pavlović S, Marinković D, Kostić M, Lončarević D, Mojović L, Stanković M, Veljković VB. The chicken eggshell calcium oxide ultrasonically dispersed over lignite coal fly ash-based cancrinite zeolite support as a catalyst for biodiesel production. in Fuel. 2021;289:119912.
doi:10.1016/j.fuel.2020.119912 .

Pavlović, Stefan, Marinković, Dalibor, Kostić, Milan, Lončarević, Davor, Mojović, Ljiljana, Stanković, Miroslav, Veljković, Vlada B., "The chicken eggshell calcium oxide ultrasonically dispersed over lignite coal fly ash-based cancrinite zeolite support as a catalyst for biodiesel production" in Fuel, 289 (2021):119912,
https://doi.org/10.1016/j.fuel.2020.119912 . .

TY  - JOUR
AU  - Vukoje, Ivana D.
AU  - Džunuzović, Enis
AU  - Lončarević, Davor R.
AU  - Dimitrijević, Suzana
AU  - Ahrenkiel, Scott Phillip
AU  - Nedeljković, Jovan
PY  - 2017
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3717
AB  - Poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate) (poly(GMA-co-EGDMA) macroporous copolymer decorated with silver nanoparticles was prepared by a modification of poly(GMA-co-EGDMA) in the reaction with arginine, and consequent reduction of silver ions with amino groups. The mercury intrusion porosimetry, transmission electron microscopy, X-ray diffraction, UV-vis reflection spectroscopy, and inductively coupled plasma atomic emission measurements were used to characterize obtained composite. The coordination of silver nanoparticles to the poly(GMA-co-EGDMA) copolymer was studied using infrared spectroscopy. Time dependence and concentration dependence of the antimicrobial efficiency of composite were tested against Gram-negative bacteria Escherichia coli, Gram-positive bacteria Staphylococcus aureus, and fungus Candida albicans. The composite ensured maximum reduction of both bacteria, while the fungi reduction reached satisfactory 96.8%. Preliminary antimicrobial efficiency measurements using laboratory flow setup indicated potential applicability of composite for wastewater treatment.
PB  - Wiley, Hoboken
T2  - Polymer Composites
T1  - Synthesis, Characterization, and Antimicrobial Activity of Silver Nanoparticles on Poly(GMA-co-EGDMA) Polymer Support
EP  - 1214
IS  - 6
SP  - 1206
VL  - 38
DO  - 10.1002/pc.23684
ER  - 

@article{
author = "Vukoje, Ivana D. and Džunuzović, Enis and Lončarević, Davor R. and Dimitrijević, Suzana and Ahrenkiel, Scott Phillip and Nedeljković, Jovan",
year = "2017",
abstract = "Poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate) (poly(GMA-co-EGDMA) macroporous copolymer decorated with silver nanoparticles was prepared by a modification of poly(GMA-co-EGDMA) in the reaction with arginine, and consequent reduction of silver ions with amino groups. The mercury intrusion porosimetry, transmission electron microscopy, X-ray diffraction, UV-vis reflection spectroscopy, and inductively coupled plasma atomic emission measurements were used to characterize obtained composite. The coordination of silver nanoparticles to the poly(GMA-co-EGDMA) copolymer was studied using infrared spectroscopy. Time dependence and concentration dependence of the antimicrobial efficiency of composite were tested against Gram-negative bacteria Escherichia coli, Gram-positive bacteria Staphylococcus aureus, and fungus Candida albicans. The composite ensured maximum reduction of both bacteria, while the fungi reduction reached satisfactory 96.8%. Preliminary antimicrobial efficiency measurements using laboratory flow setup indicated potential applicability of composite for wastewater treatment.",
publisher = "Wiley, Hoboken",
journal = "Polymer Composites",
title = "Synthesis, Characterization, and Antimicrobial Activity of Silver Nanoparticles on Poly(GMA-co-EGDMA) Polymer Support",
pages = "1214-1206",
number = "6",
volume = "38",
doi = "10.1002/pc.23684"
}

Vukoje, I. D., Džunuzović, E., Lončarević, D. R., Dimitrijević, S., Ahrenkiel, S. P.,& Nedeljković, J.. (2017). Synthesis, Characterization, and Antimicrobial Activity of Silver Nanoparticles on Poly(GMA-co-EGDMA) Polymer Support. in Polymer Composites
Wiley, Hoboken., 38(6), 1206-1214.
https://doi.org/10.1002/pc.23684

Vukoje ID, Džunuzović E, Lončarević DR, Dimitrijević S, Ahrenkiel SP, Nedeljković J. Synthesis, Characterization, and Antimicrobial Activity of Silver Nanoparticles on Poly(GMA-co-EGDMA) Polymer Support. in Polymer Composites. 2017;38(6):1206-1214.
doi:10.1002/pc.23684 .

Vukoje, Ivana D., Džunuzović, Enis, Lončarević, Davor R., Dimitrijević, Suzana, Ahrenkiel, Scott Phillip, Nedeljković, Jovan, "Synthesis, Characterization, and Antimicrobial Activity of Silver Nanoparticles on Poly(GMA-co-EGDMA) Polymer Support" in Polymer Composites, 38, no. 6 (2017):1206-1214,
https://doi.org/10.1002/pc.23684 . .

TY  - JOUR
AU  - Lončarević, Davor
AU  - Vukoje, Ivana D.
AU  - Dostanić, Jasmina
AU  - Bjelajac, Anđelika
AU  - Đorđević, Vesna R.
AU  - Dimitrijević, Suzana
AU  - Nedeljković, Jovan
PY  - 2017
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3742
AB  - The rod-like Ag2CO3 particles (2-4 3 0.3-0.6 mm, length 3 diameter) were synthesized in water by the precipitation reaction between AgNO3 and NaHCO3 in the presence of polyvinylpyrrolidone. The X-ray diffraction analysis revealed the co-existence of monoclinic and hexagonal phases of Ag2CO3, without presence of impurities. The band gap energy of Ag-2 CO3 was found to be 1.4 eV from the diffuse reflectance spectra. Photocatalytic ability of Ag2CO3 was tested using degradation reaction of the organic dye methylene blue over the wide range of concentrations, as well as under long run working conditions in repeated cycles. The photocatalytic mechanism was discussed in terms of the relative energetics of valence and conduction band. Antimicrobial efficiency of Ag-2 CO3 in dark was tested against Gram-negative bacteria E. coli. The Ag2CO3 dispersions in the concentration range 0.1-1.0 mg/mL ensured 100% reduction of bacteria cells. Time-dependent measurements revealed that reduction rates of bacteria cells vary in ascending order with the content of Ag2CO3. On the other hand, the observed reduction rates of bacteria cells do not depend on the concentration of coexisting free Ag+ ions (from 2 to 25 mg/L) present in Ag2CO3 dispersion.
PB  - Wiley-VCH Verlag Gmbh, Weinheim
T2  - Chemistryselect
T1  - Antimicrobial and Photocatalytic Abilities of Ag2CO3 Nano-Rods
EP  - 2938
IS  - 10
SP  - 2931
VL  - 2
DO  - 10.1002/slct.201700003
ER  - 

@article{
author = "Lončarević, Davor and Vukoje, Ivana D. and Dostanić, Jasmina and Bjelajac, Anđelika and Đorđević, Vesna R. and Dimitrijević, Suzana and Nedeljković, Jovan",
year = "2017",
abstract = "The rod-like Ag2CO3 particles (2-4 3 0.3-0.6 mm, length 3 diameter) were synthesized in water by the precipitation reaction between AgNO3 and NaHCO3 in the presence of polyvinylpyrrolidone. The X-ray diffraction analysis revealed the co-existence of monoclinic and hexagonal phases of Ag2CO3, without presence of impurities. The band gap energy of Ag-2 CO3 was found to be 1.4 eV from the diffuse reflectance spectra. Photocatalytic ability of Ag2CO3 was tested using degradation reaction of the organic dye methylene blue over the wide range of concentrations, as well as under long run working conditions in repeated cycles. The photocatalytic mechanism was discussed in terms of the relative energetics of valence and conduction band. Antimicrobial efficiency of Ag-2 CO3 in dark was tested against Gram-negative bacteria E. coli. The Ag2CO3 dispersions in the concentration range 0.1-1.0 mg/mL ensured 100% reduction of bacteria cells. Time-dependent measurements revealed that reduction rates of bacteria cells vary in ascending order with the content of Ag2CO3. On the other hand, the observed reduction rates of bacteria cells do not depend on the concentration of coexisting free Ag+ ions (from 2 to 25 mg/L) present in Ag2CO3 dispersion.",
publisher = "Wiley-VCH Verlag Gmbh, Weinheim",
journal = "Chemistryselect",
title = "Antimicrobial and Photocatalytic Abilities of Ag2CO3 Nano-Rods",
pages = "2938-2931",
number = "10",
volume = "2",
doi = "10.1002/slct.201700003"
}

Lončarević, D., Vukoje, I. D., Dostanić, J., Bjelajac, A., Đorđević, V. R., Dimitrijević, S.,& Nedeljković, J.. (2017). Antimicrobial and Photocatalytic Abilities of Ag2CO3 Nano-Rods. in Chemistryselect
Wiley-VCH Verlag Gmbh, Weinheim., 2(10), 2931-2938.
https://doi.org/10.1002/slct.201700003

Lončarević D, Vukoje ID, Dostanić J, Bjelajac A, Đorđević VR, Dimitrijević S, Nedeljković J. Antimicrobial and Photocatalytic Abilities of Ag2CO3 Nano-Rods. in Chemistryselect. 2017;2(10):2931-2938.
doi:10.1002/slct.201700003 .

Lončarević, Davor, Vukoje, Ivana D., Dostanić, Jasmina, Bjelajac, Anđelika, Đorđević, Vesna R., Dimitrijević, Suzana, Nedeljković, Jovan, "Antimicrobial and Photocatalytic Abilities of Ag2CO3 Nano-Rods" in Chemistryselect, 2, no. 10 (2017):2931-2938,
https://doi.org/10.1002/slct.201700003 . .

TY  - JOUR
AU  - Vukoje, Ivana D.
AU  - Kovač, Tijana
AU  - Džunuzović, Jasna
AU  - Džunuzović, Enis
AU  - Lončarević, Davor
AU  - Ahrenkiel, Scott Phillip
AU  - Nedeljković, Jovan
PY  - 2016
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3453
AB  - The synthetic procedures for preparation of free-standing and attached to polymer support surface modified TiO2 nanoparticles (NPs) with absorption extended into the visible spectral region due to charge transfer complex formation were developed. The one-step synthesis of colloids consisting of surface-modified TiO2 NPs is based on the reaction between titanium(IV) isopropoxide (TTIP) and lauryl galatte in nonprotic organic solvents (tetrahydrofuran, xylol, chloroform). The poly(GMA-co-EGDMA) copolymer decorated with surface-modified TiO2 NPs was obtained in two steps. First, copolymer was functionalized with dopamine and then treated with TTIP in organic solvent at slightly elevated temperature. Thorough microstructural and optical characterization of free-standing and attached to polymer support surface-modified TiO2 NPs was performed involving transmission electron microscopy as well as absorption and reflection spectroscopy. Infrared spectroscopy was used to understand coordination of ligands to surface Ti atoms. Photoredox chemistry of surface-modified TiO2 NPs attached to the polymer support was tested. Enhanced photooxidative ability of composite was demonstrated by degradation of organic dye crystal violet under visible light illumination, i.e., using photons with energy smaller than 2.75 eV. On the other hand, photocatalytic hydrogen production was used to demonstrate photoreduction ability of surface modified TiO2 NPs attached to the polymer support.
PB  - Amer Chemical Soc, Washington
T2  - Journal of Physical Chemistry C
T1  - Photocatalytic Ability of Visible-Light-Responsive TiO2 Nanoparticles
EP  - 18569
IS  - 33
SP  - 18560
VL  - 120
DO  - 10.1021/acs.jpcc.6b04293
ER  - 

@article{
author = "Vukoje, Ivana D. and Kovač, Tijana and Džunuzović, Jasna and Džunuzović, Enis and Lončarević, Davor and Ahrenkiel, Scott Phillip and Nedeljković, Jovan",
year = "2016",
abstract = "The synthetic procedures for preparation of free-standing and attached to polymer support surface modified TiO2 nanoparticles (NPs) with absorption extended into the visible spectral region due to charge transfer complex formation were developed. The one-step synthesis of colloids consisting of surface-modified TiO2 NPs is based on the reaction between titanium(IV) isopropoxide (TTIP) and lauryl galatte in nonprotic organic solvents (tetrahydrofuran, xylol, chloroform). The poly(GMA-co-EGDMA) copolymer decorated with surface-modified TiO2 NPs was obtained in two steps. First, copolymer was functionalized with dopamine and then treated with TTIP in organic solvent at slightly elevated temperature. Thorough microstructural and optical characterization of free-standing and attached to polymer support surface-modified TiO2 NPs was performed involving transmission electron microscopy as well as absorption and reflection spectroscopy. Infrared spectroscopy was used to understand coordination of ligands to surface Ti atoms. Photoredox chemistry of surface-modified TiO2 NPs attached to the polymer support was tested. Enhanced photooxidative ability of composite was demonstrated by degradation of organic dye crystal violet under visible light illumination, i.e., using photons with energy smaller than 2.75 eV. On the other hand, photocatalytic hydrogen production was used to demonstrate photoreduction ability of surface modified TiO2 NPs attached to the polymer support.",
publisher = "Amer Chemical Soc, Washington",
journal = "Journal of Physical Chemistry C",
title = "Photocatalytic Ability of Visible-Light-Responsive TiO2 Nanoparticles",
pages = "18569-18560",
number = "33",
volume = "120",
doi = "10.1021/acs.jpcc.6b04293"
}

Vukoje, I. D., Kovač, T., Džunuzović, J., Džunuzović, E., Lončarević, D., Ahrenkiel, S. P.,& Nedeljković, J.. (2016). Photocatalytic Ability of Visible-Light-Responsive TiO2 Nanoparticles. in Journal of Physical Chemistry C
Amer Chemical Soc, Washington., 120(33), 18560-18569.
https://doi.org/10.1021/acs.jpcc.6b04293

Vukoje ID, Kovač T, Džunuzović J, Džunuzović E, Lončarević D, Ahrenkiel SP, Nedeljković J. Photocatalytic Ability of Visible-Light-Responsive TiO2 Nanoparticles. in Journal of Physical Chemistry C. 2016;120(33):18560-18569.
doi:10.1021/acs.jpcc.6b04293 .

Vukoje, Ivana D., Kovač, Tijana, Džunuzović, Jasna, Džunuzović, Enis, Lončarević, Davor, Ahrenkiel, Scott Phillip, Nedeljković, Jovan, "Photocatalytic Ability of Visible-Light-Responsive TiO2 Nanoparticles" in Journal of Physical Chemistry C, 120, no. 33 (2016):18560-18569,
https://doi.org/10.1021/acs.jpcc.6b04293 . .

TY  - JOUR
AU  - Dostanić, Jasmina
AU  - Mijin, Dušan
AU  - Ušćumlić, Gordana
AU  - Jovanović, Dušan M.
AU  - Zlatar, Matija
AU  - Lončarević, Davor
PY  - 2014
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/2842
AB  - A series of 5-(4-substituted arylazo)-6-hydroxy-4-methyl-3-cyano-2-pyridone dyes was synthesized and the structure of the dyes was confirmed by UV-Vis, FT-IR, H-1 NMR and C-13 NMR spectroscopic techniques. The azo-hydrazone tautomeric equilibrium was found to depend on the substituents as well as on the acidity and basicity of the media. Ionization constant, pK(a), of the dyes was determined by UV-Vis spectroscopy and correlated with the Hammett substituent constants, sigma(p) and sigma(I). The interpretation of the effect of different substituent in phenyl ring of arylazo pyridone dyes on their spectroscopic and structural properties was based on quantum chemical calculations performed by the density functional theory (DET/M06-2X) method. The DFT calculations confirmed the existence of two forms in water solution: hydrazone form in acidic and neutral media and anionic form in basic media. The different contribution of azo and hydrazone canonical forms of anionic form is observed for dyes with electron-donating and dyes with electron-withdrawing groups. The dependence of absorption spectra and determined pK(a) values to the substituent type seems to be mostly due to azo/hydrazone canonical structure ratio in their anionic form.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Spectrochimica Acta Part A-Molecular and Biomolecular Spectroscopy
T1  - Spectroscopic and quantum chemical investigations of substituent effects on the azo-hydrazone tautomerism and acid-base properties of arylazo pyridone dyes
EP  - 45
SP  - 37
VL  - 123
DO  - 10.1016/j.saa.2013.12.064
ER  - 

@article{
author = "Dostanić, Jasmina and Mijin, Dušan and Ušćumlić, Gordana and Jovanović, Dušan M. and Zlatar, Matija and Lončarević, Davor",
year = "2014",
abstract = "A series of 5-(4-substituted arylazo)-6-hydroxy-4-methyl-3-cyano-2-pyridone dyes was synthesized and the structure of the dyes was confirmed by UV-Vis, FT-IR, H-1 NMR and C-13 NMR spectroscopic techniques. The azo-hydrazone tautomeric equilibrium was found to depend on the substituents as well as on the acidity and basicity of the media. Ionization constant, pK(a), of the dyes was determined by UV-Vis spectroscopy and correlated with the Hammett substituent constants, sigma(p) and sigma(I). The interpretation of the effect of different substituent in phenyl ring of arylazo pyridone dyes on their spectroscopic and structural properties was based on quantum chemical calculations performed by the density functional theory (DET/M06-2X) method. The DFT calculations confirmed the existence of two forms in water solution: hydrazone form in acidic and neutral media and anionic form in basic media. The different contribution of azo and hydrazone canonical forms of anionic form is observed for dyes with electron-donating and dyes with electron-withdrawing groups. The dependence of absorption spectra and determined pK(a) values to the substituent type seems to be mostly due to azo/hydrazone canonical structure ratio in their anionic form.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Spectrochimica Acta Part A-Molecular and Biomolecular Spectroscopy",
title = "Spectroscopic and quantum chemical investigations of substituent effects on the azo-hydrazone tautomerism and acid-base properties of arylazo pyridone dyes",
pages = "45-37",
volume = "123",
doi = "10.1016/j.saa.2013.12.064"
}

Dostanić, J., Mijin, D., Ušćumlić, G., Jovanović, D. M., Zlatar, M.,& Lončarević, D.. (2014). Spectroscopic and quantum chemical investigations of substituent effects on the azo-hydrazone tautomerism and acid-base properties of arylazo pyridone dyes. in Spectrochimica Acta Part A-Molecular and Biomolecular Spectroscopy
Pergamon-Elsevier Science Ltd, Oxford., 123, 37-45.
https://doi.org/10.1016/j.saa.2013.12.064

Dostanić J, Mijin D, Ušćumlić G, Jovanović DM, Zlatar M, Lončarević D. Spectroscopic and quantum chemical investigations of substituent effects on the azo-hydrazone tautomerism and acid-base properties of arylazo pyridone dyes. in Spectrochimica Acta Part A-Molecular and Biomolecular Spectroscopy. 2014;123:37-45.
doi:10.1016/j.saa.2013.12.064 .

Dostanić, Jasmina, Mijin, Dušan, Ušćumlić, Gordana, Jovanović, Dušan M., Zlatar, Matija, Lončarević, Davor, "Spectroscopic and quantum chemical investigations of substituent effects on the azo-hydrazone tautomerism and acid-base properties of arylazo pyridone dyes" in Spectrochimica Acta Part A-Molecular and Biomolecular Spectroscopy, 123 (2014):37-45,
https://doi.org/10.1016/j.saa.2013.12.064 . .

TY  - JOUR
AU  - Dostanić, Jasmina
AU  - Lončarević, Davor
AU  - Rožić, Ljiljana
AU  - Petrović, Srđan
AU  - Mijin, Dušan
AU  - Jovanović, Dušan M.
PY  - 2013
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/2517
AB  - Response surface methodology (RSM) and central composite design have been applied to describe and optimize photocatalytic degradation of azo pyridone dye using TiO2, H2O2, and simulated sun light. The mutual interactions between three independent variables, viz. H2O2 concentration, irradiation time, and TiO2 content were obtained. The results revealed that the most influential variables under selected reaction conditions were irradiation time and TiO2 content. The optimized conditions for the photocatalytic degradation of azo pyridone dye were as follows: H2O2 concentration: 130.5 mg/L, irradiation time: 54.8 min, and TiO2 content: 2.48 g/L. Under these conditions, the maximum decolorization efficiency of 96.43% was achieved. This experimental value was in good agreement with the predicted one, which proved the validity of the model. Operation cost analysis indicated that irradiation time had the major influence on total process cost. The RSM based on the central composite design was shown to be a successful technique for the optimization of the decolorization efficiency of azo pyridone dye and can be very helpful in improving the process economic feasibility. TOC analysis showed that the dye could be effectively mineralized during photocatalytic degradation.
PB  - Desalination Publ, Hopkinton
T2  - Desalination and Water Treatment
T1  - Photocatalytic degradation of azo pyridone dye: Optimization using response surface methodology
EP  - 2812
IS  - 13-15
SP  - 2802
VL  - 51
DO  - 10.1080/19443994.2012.750699
ER  - 

@article{
author = "Dostanić, Jasmina and Lončarević, Davor and Rožić, Ljiljana and Petrović, Srđan and Mijin, Dušan and Jovanović, Dušan M.",
year = "2013",
abstract = "Response surface methodology (RSM) and central composite design have been applied to describe and optimize photocatalytic degradation of azo pyridone dye using TiO2, H2O2, and simulated sun light. The mutual interactions between three independent variables, viz. H2O2 concentration, irradiation time, and TiO2 content were obtained. The results revealed that the most influential variables under selected reaction conditions were irradiation time and TiO2 content. The optimized conditions for the photocatalytic degradation of azo pyridone dye were as follows: H2O2 concentration: 130.5 mg/L, irradiation time: 54.8 min, and TiO2 content: 2.48 g/L. Under these conditions, the maximum decolorization efficiency of 96.43% was achieved. This experimental value was in good agreement with the predicted one, which proved the validity of the model. Operation cost analysis indicated that irradiation time had the major influence on total process cost. The RSM based on the central composite design was shown to be a successful technique for the optimization of the decolorization efficiency of azo pyridone dye and can be very helpful in improving the process economic feasibility. TOC analysis showed that the dye could be effectively mineralized during photocatalytic degradation.",
publisher = "Desalination Publ, Hopkinton",
journal = "Desalination and Water Treatment",
title = "Photocatalytic degradation of azo pyridone dye: Optimization using response surface methodology",
pages = "2812-2802",
number = "13-15",
volume = "51",
doi = "10.1080/19443994.2012.750699"
}

Dostanić, J., Lončarević, D., Rožić, L., Petrović, S., Mijin, D.,& Jovanović, D. M.. (2013). Photocatalytic degradation of azo pyridone dye: Optimization using response surface methodology. in Desalination and Water Treatment
Desalination Publ, Hopkinton., 51(13-15), 2802-2812.
https://doi.org/10.1080/19443994.2012.750699

Dostanić J, Lončarević D, Rožić L, Petrović S, Mijin D, Jovanović DM. Photocatalytic degradation of azo pyridone dye: Optimization using response surface methodology. in Desalination and Water Treatment. 2013;51(13-15):2802-2812.
doi:10.1080/19443994.2012.750699 .

Dostanić, Jasmina, Lončarević, Davor, Rožić, Ljiljana, Petrović, Srđan, Mijin, Dušan, Jovanović, Dušan M., "Photocatalytic degradation of azo pyridone dye: Optimization using response surface methodology" in Desalination and Water Treatment, 51, no. 13-15 (2013):2802-2812,
https://doi.org/10.1080/19443994.2012.750699 . .

TY  - JOUR
AU  - Dostanić, Jasmina
AU  - Lončarević, Davor
AU  - Banković, Predrag
AU  - Cvetković, Olga
AU  - Jovanović, Dušan M.
AU  - Mijin, Dušan
PY  - 2011
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1924
AB  - Photocatalytic degradation of synthesized azo pyridone dye (5-(4-sulpho phenylazo)-6-hydroxy-4-methyl-3-cyano-2-pyridone), in aqueous solutions by simulated sunlight in the presence of commercial TiO2, Aeroxide P25, was studied. The reaction kinetics analysis showed that photodegradation exhibits pseudo first-order kinetics according to Langmuir-Hinshelwood model. The effects of various process parameters on the photocatalytic degradation were investigated. The optimal catalyst content and pH were determined. A decrease in the reaction rate was observed upon the increase of the initial dye concentration. Degradation of the dye was enhanced by hydrogen peroxide, but it was inhibited by ethanol. The influence of temperature was studied, and the energy of activation was determined. According to total organic carbon (TOC) analysis, 54% of TOC remained when 100% of the dye was decolorized. Although the intermediates were not determined in this study, the TOC results clearly indicate their presence during the reaction. In addition, photocatalytic degradation of simulated dyehouse effluents, containing tested azo pyridone dye and associated auxiliary chemicals was investigated.
PB  - Taylor & Francis Inc, Philadelphia
T2  - Journal of Environmental Science and Health Part A-Toxic/Hazardous Substances & Environmental Engine
T1  - Influence of process parameters on the photodegradation of synthesized azo pyridone dye in TiO2 water suspension under simulated sunlight
EP  - 79
IS  - 1
SP  - 70
VL  - 46
DO  - 10.1080/10934529.2011.526905
ER  - 

@article{
author = "Dostanić, Jasmina and Lončarević, Davor and Banković, Predrag and Cvetković, Olga and Jovanović, Dušan M. and Mijin, Dušan",
year = "2011",
abstract = "Photocatalytic degradation of synthesized azo pyridone dye (5-(4-sulpho phenylazo)-6-hydroxy-4-methyl-3-cyano-2-pyridone), in aqueous solutions by simulated sunlight in the presence of commercial TiO2, Aeroxide P25, was studied. The reaction kinetics analysis showed that photodegradation exhibits pseudo first-order kinetics according to Langmuir-Hinshelwood model. The effects of various process parameters on the photocatalytic degradation were investigated. The optimal catalyst content and pH were determined. A decrease in the reaction rate was observed upon the increase of the initial dye concentration. Degradation of the dye was enhanced by hydrogen peroxide, but it was inhibited by ethanol. The influence of temperature was studied, and the energy of activation was determined. According to total organic carbon (TOC) analysis, 54% of TOC remained when 100% of the dye was decolorized. Although the intermediates were not determined in this study, the TOC results clearly indicate their presence during the reaction. In addition, photocatalytic degradation of simulated dyehouse effluents, containing tested azo pyridone dye and associated auxiliary chemicals was investigated.",
publisher = "Taylor & Francis Inc, Philadelphia",
journal = "Journal of Environmental Science and Health Part A-Toxic/Hazardous Substances & Environmental Engine",
title = "Influence of process parameters on the photodegradation of synthesized azo pyridone dye in TiO2 water suspension under simulated sunlight",
pages = "79-70",
number = "1",
volume = "46",
doi = "10.1080/10934529.2011.526905"
}

Dostanić, J., Lončarević, D., Banković, P., Cvetković, O., Jovanović, D. M.,& Mijin, D.. (2011). Influence of process parameters on the photodegradation of synthesized azo pyridone dye in TiO2 water suspension under simulated sunlight. in Journal of Environmental Science and Health Part A-Toxic/Hazardous Substances & Environmental Engine
Taylor & Francis Inc, Philadelphia., 46(1), 70-79.
https://doi.org/10.1080/10934529.2011.526905

Dostanić J, Lončarević D, Banković P, Cvetković O, Jovanović DM, Mijin D. Influence of process parameters on the photodegradation of synthesized azo pyridone dye in TiO2 water suspension under simulated sunlight. in Journal of Environmental Science and Health Part A-Toxic/Hazardous Substances & Environmental Engine. 2011;46(1):70-79.
doi:10.1080/10934529.2011.526905 .

Dostanić, Jasmina, Lončarević, Davor, Banković, Predrag, Cvetković, Olga, Jovanović, Dušan M., Mijin, Dušan, "Influence of process parameters on the photodegradation of synthesized azo pyridone dye in TiO2 water suspension under simulated sunlight" in Journal of Environmental Science and Health Part A-Toxic/Hazardous Substances & Environmental Engine, 46, no. 1 (2011):70-79,
https://doi.org/10.1080/10934529.2011.526905 . .