TY  - JOUR
AU  - Krupez, Jelena
AU  - Kovačević, Vesna V.
AU  - Jović, Milica
AU  - Roglić, Goran
AU  - Natić, Maja
AU  - Kuraica, Milorad M.
AU  - Obradović, Bratislav M.
AU  - Dojčinović, Biljana
PY  - 2018
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2338
AB  - Nicotine degradation efficiency in water solutions was studied using a water falling film dielectric barrier discharge (DBD) reactor. Two different treatments were applied: direct treatment, the recirculation of the solution through a DBD reactor, and indirect treatment, the bubbling of the gas from the DBD through the porous filter into the solution. In a separate experiment, samples spiked with nicotine in double distilled water (ddH(2)O) and tap water were studied and compared after both treatments. Furthermore, the effects of the homogeneous catalysts, namely, Fe2+ and H2O2, were tested in the direct treatment. Nicotine degradation efficiency was determined using high-performance liquid chromatography. A degradation efficiency of 90% was achieved after the direct treatment catalyzed with Fe2+. In order to analyze the biodegradability, mineralization level, and toxicity of the obtained solutions, after all degradation procedures the values of the following parameters were determined: total organic carbon, chemical oxygen demand, biochemical oxygen demand, and the Artemia salina toxicity test. The results showed that an increase in biodegradability was obtained, after all treatments. A partial nicotine mineralization was achieved and the mortality of the A. salina organism decreased in the treated samples, all of which indicating the effective removal of nicotine and the creation of less toxic solutions. Nicotine degradation products were identified using ultrahigh-performance liquid chromatography coupled with a linear ion trap Orbitrap hybrid mass spectrometer and a simple mechanism for oxidative degradation of nicotine in non-thermal plasma systems is proposed.
PB  - Iop Publishing Ltd, Bristol
T2  - Journal of Physics D-Applied Physics
T1  - Degradation of nicotine in water solutions using a water falling film DBD plasma reactor: direct and indirect treatment
VL  - 51
IS  - 17
DO  - 10.1088/1361-6463/aab632
ER  - 

@article{
author = "Krupez, Jelena and Kovačević, Vesna V. and Jović, Milica and Roglić, Goran and Natić, Maja and Kuraica, Milorad M. and Obradović, Bratislav M. and Dojčinović, Biljana",
year = "2018",
abstract = "Nicotine degradation efficiency in water solutions was studied using a water falling film dielectric barrier discharge (DBD) reactor. Two different treatments were applied: direct treatment, the recirculation of the solution through a DBD reactor, and indirect treatment, the bubbling of the gas from the DBD through the porous filter into the solution. In a separate experiment, samples spiked with nicotine in double distilled water (ddH(2)O) and tap water were studied and compared after both treatments. Furthermore, the effects of the homogeneous catalysts, namely, Fe2+ and H2O2, were tested in the direct treatment. Nicotine degradation efficiency was determined using high-performance liquid chromatography. A degradation efficiency of 90% was achieved after the direct treatment catalyzed with Fe2+. In order to analyze the biodegradability, mineralization level, and toxicity of the obtained solutions, after all degradation procedures the values of the following parameters were determined: total organic carbon, chemical oxygen demand, biochemical oxygen demand, and the Artemia salina toxicity test. The results showed that an increase in biodegradability was obtained, after all treatments. A partial nicotine mineralization was achieved and the mortality of the A. salina organism decreased in the treated samples, all of which indicating the effective removal of nicotine and the creation of less toxic solutions. Nicotine degradation products were identified using ultrahigh-performance liquid chromatography coupled with a linear ion trap Orbitrap hybrid mass spectrometer and a simple mechanism for oxidative degradation of nicotine in non-thermal plasma systems is proposed.",
publisher = "Iop Publishing Ltd, Bristol",
journal = "Journal of Physics D-Applied Physics",
title = "Degradation of nicotine in water solutions using a water falling film DBD plasma reactor: direct and indirect treatment",
volume = "51",
number = "17",
doi = "10.1088/1361-6463/aab632"
}

Krupez, J., Kovačević, V. V., Jović, M., Roglić, G., Natić, M., Kuraica, M. M., Obradović, B. M.,& Dojčinović, B.. (2018). Degradation of nicotine in water solutions using a water falling film DBD plasma reactor: direct and indirect treatment. in Journal of Physics D-Applied Physics
Iop Publishing Ltd, Bristol., 51(17).
https://doi.org/10.1088/1361-6463/aab632

Krupez J, Kovačević VV, Jović M, Roglić G, Natić M, Kuraica MM, Obradović BM, Dojčinović B. Degradation of nicotine in water solutions using a water falling film DBD plasma reactor: direct and indirect treatment. in Journal of Physics D-Applied Physics. 2018;51(17).
doi:10.1088/1361-6463/aab632 .

Krupez, Jelena, Kovačević, Vesna V., Jović, Milica, Roglić, Goran, Natić, Maja, Kuraica, Milorad M., Obradović, Bratislav M., Dojčinović, Biljana, "Degradation of nicotine in water solutions using a water falling film DBD plasma reactor: direct and indirect treatment" in Journal of Physics D-Applied Physics, 51, no. 17 (2018),
https://doi.org/10.1088/1361-6463/aab632 . .

TY  - JOUR
AU  - Sentić, Milica
AU  - Sojic, Neso
AU  - Paolucci, Francesco
AU  - Arbault, Stéphane
AU  - Rapino, Stefania
AU  - Villani, Elena
AU  - Jović, Milica
AU  - Lesch, Andreas
AU  - Goudeau, Bertrand
AU  - Scarabino, Sabina
AU  - Giovanni, Valenti
PY  - 2017
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/7132
AB  - We report here the development of coreactant-based electrogenerated chemiluminescence (ECL) as a surface-confined microscopy to image single cells and their membrane proteins. Labeling the entire cell membrane allows one to demonstrate that, by contrast with fluorescence, ECL emission is only detected from fluorophores located in the immediate vicinity of the electrode surface (i.e., 1–2 μm). Then, to present the potential diagnostic applications of our approach, we selected carbon nanotubes (CNT)-based inkjet-printed disposable electrodes for the direct ECL imaging of a labeled plasma receptor overexpressed on tumor cells. The ECL fluorophore was linked to an antibody and enabled to localize the ECL generation on the cancer cell membrane in close proximity to the electrode surface. Such a result is intrinsically associated with the unique ECL mechanism and is rationalized by considering the limited lifetimes of the electrogenerated coreactant radicals. The electrochemical stimulus used for luminescence generation does not suffer from background signals, such as the typical autofluorescence of biological samples. The presented surface-confined ECL microscopy should find promising applications in ultrasensitive single cell imaging assays.
PB  - American Chemical Society (ACS)
T2  - Journal of the American Chemical Society
T1  - Single Cell Electrochemiluminescence Imaging: From the Proof-of-Concept to Disposable Device-Based Analysis
VL  - 139
IS  - 46
SP  - 16830
EP  - 16837
DO  - 10.1021/jacs.7b09260
ER  - 

@article{
author = "Sentić, Milica and Sojic, Neso and Paolucci, Francesco and Arbault, Stéphane and Rapino, Stefania and Villani, Elena and Jović, Milica and Lesch, Andreas and Goudeau, Bertrand and Scarabino, Sabina and Giovanni, Valenti",
year = "2017",
abstract = "We report here the development of coreactant-based electrogenerated chemiluminescence (ECL) as a surface-confined microscopy to image single cells and their membrane proteins. Labeling the entire cell membrane allows one to demonstrate that, by contrast with fluorescence, ECL emission is only detected from fluorophores located in the immediate vicinity of the electrode surface (i.e., 1–2 μm). Then, to present the potential diagnostic applications of our approach, we selected carbon nanotubes (CNT)-based inkjet-printed disposable electrodes for the direct ECL imaging of a labeled plasma receptor overexpressed on tumor cells. The ECL fluorophore was linked to an antibody and enabled to localize the ECL generation on the cancer cell membrane in close proximity to the electrode surface. Such a result is intrinsically associated with the unique ECL mechanism and is rationalized by considering the limited lifetimes of the electrogenerated coreactant radicals. The electrochemical stimulus used for luminescence generation does not suffer from background signals, such as the typical autofluorescence of biological samples. The presented surface-confined ECL microscopy should find promising applications in ultrasensitive single cell imaging assays.",
publisher = "American Chemical Society (ACS)",
journal = "Journal of the American Chemical Society",
title = "Single Cell Electrochemiluminescence Imaging: From the Proof-of-Concept to Disposable Device-Based Analysis",
volume = "139",
number = "46",
pages = "16830-16837",
doi = "10.1021/jacs.7b09260"
}

Sentić, M., Sojic, N., Paolucci, F., Arbault, S., Rapino, S., Villani, E., Jović, M., Lesch, A., Goudeau, B., Scarabino, S.,& Giovanni, V.. (2017). Single Cell Electrochemiluminescence Imaging: From the Proof-of-Concept to Disposable Device-Based Analysis. in Journal of the American Chemical Society
American Chemical Society (ACS)., 139(46), 16830-16837.
https://doi.org/10.1021/jacs.7b09260

Sentić M, Sojic N, Paolucci F, Arbault S, Rapino S, Villani E, Jović M, Lesch A, Goudeau B, Scarabino S, Giovanni V. Single Cell Electrochemiluminescence Imaging: From the Proof-of-Concept to Disposable Device-Based Analysis. in Journal of the American Chemical Society. 2017;139(46):16830-16837.
doi:10.1021/jacs.7b09260 .

Sentić, Milica, Sojic, Neso, Paolucci, Francesco, Arbault, Stéphane, Rapino, Stefania, Villani, Elena, Jović, Milica, Lesch, Andreas, Goudeau, Bertrand, Scarabino, Sabina, Giovanni, Valenti, "Single Cell Electrochemiluminescence Imaging: From the Proof-of-Concept to Disposable Device-Based Analysis" in Journal of the American Chemical Society, 139, no. 46 (2017):16830-16837,
https://doi.org/10.1021/jacs.7b09260 . .

TY  - JOUR
AU  - Kovačević, Vesna V.
AU  - Dojčinović, Biljana
AU  - Jović, Milica
AU  - Roglić, Goran
AU  - Obradović, Bratislav M.
AU  - Kuraica, Milorad M.
PY  - 2017
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2227
AB  - The formation of hydroxyl radical and long-living chemical species (H2O2, O-3, NO3- and NO2-) generated in the liquid phase of a water falling film dielectric barrier discharge in dependence on the gas atmosphere (air, nitrogen, oxygen, argon and helium) was studied. The chemical molecular probe dimethyl sulfoxide was employed for quantification of. OH, and the influence of hydroxyl radical scavenging on formation of reactive oxygen and nitrogen species was investigated. In addition to liquid analysis, plasma diagnostics was applied to indicate possible reaction pathways of plasma-liquid interaction. The highest. OH production rate of 1.19 x 10 (5) mol l (1) s (1) was found when water was treated in oxygen, with a yield of 2.75 x 10(-2) molecules of. OH per 100 eV. Formation of hydrogen peroxide in air, nitrogen and argon discharges is determined by recombination reaction of hydroxyl radicals, reaching the highest yield of about 0.7 g kWh(-1) when distilled water was treated in argon discharge. Ozone formation was dominant in oxygen and air discharges. Strong acidification along with formation of reactive nitrogen species was detected in water treated in air and nitrogen discharges.
PB  - Iop Publishing Ltd, Bristol
T2  - Journal of Physics D-Applied Physics
T1  - Measurement of reactive species generated by dielectric barrier discharge in direct contact with water in different atmospheres
VL  - 50
IS  - 15
DO  - 10.1088/1361-6463/aa5fde
ER  - 

@article{
author = "Kovačević, Vesna V. and Dojčinović, Biljana and Jović, Milica and Roglić, Goran and Obradović, Bratislav M. and Kuraica, Milorad M.",
year = "2017",
abstract = "The formation of hydroxyl radical and long-living chemical species (H2O2, O-3, NO3- and NO2-) generated in the liquid phase of a water falling film dielectric barrier discharge in dependence on the gas atmosphere (air, nitrogen, oxygen, argon and helium) was studied. The chemical molecular probe dimethyl sulfoxide was employed for quantification of. OH, and the influence of hydroxyl radical scavenging on formation of reactive oxygen and nitrogen species was investigated. In addition to liquid analysis, plasma diagnostics was applied to indicate possible reaction pathways of plasma-liquid interaction. The highest. OH production rate of 1.19 x 10 (5) mol l (1) s (1) was found when water was treated in oxygen, with a yield of 2.75 x 10(-2) molecules of. OH per 100 eV. Formation of hydrogen peroxide in air, nitrogen and argon discharges is determined by recombination reaction of hydroxyl radicals, reaching the highest yield of about 0.7 g kWh(-1) when distilled water was treated in argon discharge. Ozone formation was dominant in oxygen and air discharges. Strong acidification along with formation of reactive nitrogen species was detected in water treated in air and nitrogen discharges.",
publisher = "Iop Publishing Ltd, Bristol",
journal = "Journal of Physics D-Applied Physics",
title = "Measurement of reactive species generated by dielectric barrier discharge in direct contact with water in different atmospheres",
volume = "50",
number = "15",
doi = "10.1088/1361-6463/aa5fde"
}

Kovačević, V. V., Dojčinović, B., Jović, M., Roglić, G., Obradović, B. M.,& Kuraica, M. M.. (2017). Measurement of reactive species generated by dielectric barrier discharge in direct contact with water in different atmospheres. in Journal of Physics D-Applied Physics
Iop Publishing Ltd, Bristol., 50(15).
https://doi.org/10.1088/1361-6463/aa5fde

Kovačević VV, Dojčinović B, Jović M, Roglić G, Obradović BM, Kuraica MM. Measurement of reactive species generated by dielectric barrier discharge in direct contact with water in different atmospheres. in Journal of Physics D-Applied Physics. 2017;50(15).
doi:10.1088/1361-6463/aa5fde .

Kovačević, Vesna V., Dojčinović, Biljana, Jović, Milica, Roglić, Goran, Obradović, Bratislav M., Kuraica, Milorad M., "Measurement of reactive species generated by dielectric barrier discharge in direct contact with water in different atmospheres" in Journal of Physics D-Applied Physics, 50, no. 15 (2017),
https://doi.org/10.1088/1361-6463/aa5fde . .

TY  - JOUR
AU  - Aonyas, Munera M
AU  - Nesic, Jelena
AU  - Jović, Milica
AU  - Marković, Marijana
AU  - Dojčinović, Biljana
AU  - Obradović, Bratislav M.
AU  - Roglić, Goran
PY  - 2016
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1952
AB  - The aim of this study was to investigate the degradation of the non-ionic surfactant Triton X-100 (TX-100) by using an advanced oxidation process in a non-thermal plasma reactor based on water falling film dielectric barrier discharge (DBD). The effects of two catalytic plasma systems, Fe2+/DBD and H2O2/DBD, were tested to improve the degradation of TX-100 and the mineralization efficiency in the DBD reactor. Both catalytic systems exhibited significant improvements in degradation efficiency, especially in the beginning of the treatment: the efficiency increased from 23 to 88 and 50%, for 5 mgL(-1) Fe2+/DBD and 10 mmol L-1 H2O2/DBD, respectively. The mineralization efficiency of TX-100 in the non-catalytic DBD treatment was very low (1%), but with addition of catalysts, the mineralization efficiency was drastically improved, with H2O2/DBD at 4-34% (depending on the H2O2 concentration) and Fe2+/DBD at 2-21% (depending on the Fe2+ concentration). Degradation products of TX-100 in non-catalytic and two catalytic systems were identified using UHPLC-Orbitrap-MS. Based on the degradation products that were identified, a simple mechanistic scheme was proposed. MS analysis revealed that degradation of TX-100 in the DBD reactor occurred by shortening the ethoxy chain. In the presence of catalysts, there are additional reactions of cleavage of the alkyl chain followed by formation of polyethoxylated phenol (H2O2/DBD) and addition of OH center dot radicals onto the aromatic ring (Fe2+/DBD). The final degradation products did not cause any significant toxic effects to Vibrio fischeri or Artemia salina.
PB  - Wiley-Blackwell, Hoboken
T2  - Clean-Soil Air Water
T1  - Degradation of Triton X-100 in Water Falling Film Dielectric Barrier Discharge Reactor
VL  - 44
IS  - 4
SP  - 422
EP  - 429
DO  - 10.1002/clen.201500501
ER  - 

@article{
author = "Aonyas, Munera M and Nesic, Jelena and Jović, Milica and Marković, Marijana and Dojčinović, Biljana and Obradović, Bratislav M. and Roglić, Goran",
year = "2016",
abstract = "The aim of this study was to investigate the degradation of the non-ionic surfactant Triton X-100 (TX-100) by using an advanced oxidation process in a non-thermal plasma reactor based on water falling film dielectric barrier discharge (DBD). The effects of two catalytic plasma systems, Fe2+/DBD and H2O2/DBD, were tested to improve the degradation of TX-100 and the mineralization efficiency in the DBD reactor. Both catalytic systems exhibited significant improvements in degradation efficiency, especially in the beginning of the treatment: the efficiency increased from 23 to 88 and 50%, for 5 mgL(-1) Fe2+/DBD and 10 mmol L-1 H2O2/DBD, respectively. The mineralization efficiency of TX-100 in the non-catalytic DBD treatment was very low (1%), but with addition of catalysts, the mineralization efficiency was drastically improved, with H2O2/DBD at 4-34% (depending on the H2O2 concentration) and Fe2+/DBD at 2-21% (depending on the Fe2+ concentration). Degradation products of TX-100 in non-catalytic and two catalytic systems were identified using UHPLC-Orbitrap-MS. Based on the degradation products that were identified, a simple mechanistic scheme was proposed. MS analysis revealed that degradation of TX-100 in the DBD reactor occurred by shortening the ethoxy chain. In the presence of catalysts, there are additional reactions of cleavage of the alkyl chain followed by formation of polyethoxylated phenol (H2O2/DBD) and addition of OH center dot radicals onto the aromatic ring (Fe2+/DBD). The final degradation products did not cause any significant toxic effects to Vibrio fischeri or Artemia salina.",
publisher = "Wiley-Blackwell, Hoboken",
journal = "Clean-Soil Air Water",
title = "Degradation of Triton X-100 in Water Falling Film Dielectric Barrier Discharge Reactor",
volume = "44",
number = "4",
pages = "422-429",
doi = "10.1002/clen.201500501"
}

Aonyas, M. M., Nesic, J., Jović, M., Marković, M., Dojčinović, B., Obradović, B. M.,& Roglić, G.. (2016). Degradation of Triton X-100 in Water Falling Film Dielectric Barrier Discharge Reactor. in Clean-Soil Air Water
Wiley-Blackwell, Hoboken., 44(4), 422-429.
https://doi.org/10.1002/clen.201500501

Aonyas MM, Nesic J, Jović M, Marković M, Dojčinović B, Obradović BM, Roglić G. Degradation of Triton X-100 in Water Falling Film Dielectric Barrier Discharge Reactor. in Clean-Soil Air Water. 2016;44(4):422-429.
doi:10.1002/clen.201500501 .

Aonyas, Munera M, Nesic, Jelena, Jović, Milica, Marković, Marijana, Dojčinović, Biljana, Obradović, Bratislav M., Roglić, Goran, "Degradation of Triton X-100 in Water Falling Film Dielectric Barrier Discharge Reactor" in Clean-Soil Air Water, 44, no. 4 (2016):422-429,
https://doi.org/10.1002/clen.201500501 . .

TY  - JOUR
AU  - Anđelković, Ivan
AU  - Jovic, Bojan
AU  - Jović, Milica
AU  - Marković, Marijana
AU  - Stanković, Dalibor
AU  - Manojlović, Dragan
AU  - Roglić, Goran
PY  - 2016
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1977
AB  - Composite material Zr-doped TiO2, suitable for the removal of arsenic from water, was synthetized with fast and simple microwave-hydrothermal method. Obtained material, Zr-TiO2, had uniform size and composition with zirconium ions incorporated into crystal structure of titanium dioxide. Synthetized composite material had large specific surface area and well-developed micropore and mesopore structure that was responsible for fast adsorption of As(III) and As(V) from water. The influence of pH on the adsorption capacity of arsenic was studied. The kinetics and isotherm experiments were also performed. The treatment of natural water sample containing high concentration of arsenic with composite material Zr-TiO2 was efficient. The concentration of arsenic was reduced to the value recommended by WHO.
PB  - Springer Heidelberg, Heidelberg
T2  - Environmental Science and Pollution Research
T1  - Microwave-hydrothermal method for the synthesis of composite materials for removal of arsenic from water
VL  - 23
IS  - 1
SP  - 469
EP  - 476
DO  - 10.1007/s11356-015-5283-z
ER  - 

@article{
author = "Anđelković, Ivan and Jovic, Bojan and Jović, Milica and Marković, Marijana and Stanković, Dalibor and Manojlović, Dragan and Roglić, Goran",
year = "2016",
abstract = "Composite material Zr-doped TiO2, suitable for the removal of arsenic from water, was synthetized with fast and simple microwave-hydrothermal method. Obtained material, Zr-TiO2, had uniform size and composition with zirconium ions incorporated into crystal structure of titanium dioxide. Synthetized composite material had large specific surface area and well-developed micropore and mesopore structure that was responsible for fast adsorption of As(III) and As(V) from water. The influence of pH on the adsorption capacity of arsenic was studied. The kinetics and isotherm experiments were also performed. The treatment of natural water sample containing high concentration of arsenic with composite material Zr-TiO2 was efficient. The concentration of arsenic was reduced to the value recommended by WHO.",
publisher = "Springer Heidelberg, Heidelberg",
journal = "Environmental Science and Pollution Research",
title = "Microwave-hydrothermal method for the synthesis of composite materials for removal of arsenic from water",
volume = "23",
number = "1",
pages = "469-476",
doi = "10.1007/s11356-015-5283-z"
}

Anđelković, I., Jovic, B., Jović, M., Marković, M., Stanković, D., Manojlović, D.,& Roglić, G.. (2016). Microwave-hydrothermal method for the synthesis of composite materials for removal of arsenic from water. in Environmental Science and Pollution Research
Springer Heidelberg, Heidelberg., 23(1), 469-476.
https://doi.org/10.1007/s11356-015-5283-z

Anđelković I, Jovic B, Jović M, Marković M, Stanković D, Manojlović D, Roglić G. Microwave-hydrothermal method for the synthesis of composite materials for removal of arsenic from water. in Environmental Science and Pollution Research. 2016;23(1):469-476.
doi:10.1007/s11356-015-5283-z .

Anđelković, Ivan, Jovic, Bojan, Jović, Milica, Marković, Marijana, Stanković, Dalibor, Manojlović, Dragan, Roglić, Goran, "Microwave-hydrothermal method for the synthesis of composite materials for removal of arsenic from water" in Environmental Science and Pollution Research, 23, no. 1 (2016):469-476,
https://doi.org/10.1007/s11356-015-5283-z . .

TY  - JOUR
AU  - Anđelković, Ivan
AU  - Stanković, Dalibor
AU  - Jović, Milica
AU  - Marković, Marijana
AU  - Krstić, Jugoslav
AU  - Manojlović, Dragan
AU  - Roglić, Goran
PY  - 2015
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1616
AB  - Microwave-hydrothermal method was used for the synthesis of TiO2 and TiO2 doped with zirconium. The method was fast and simple and adsorbents were used for removal of As(III) and As(V) from aqueous solutions. The adsorbents were characterized by BET surface area measurements and powder XRD. Experiments showed that TiO2 doped with 10% of Zr using the microwave-hydrothermal method have greater specific surface area and total pore volume in comparison with TiO2 synthesized using the same method. Better removal with doped adsorbent was obtained for both, As(III) and As(V). Further experiments were carried out with Zr doped TiO2 sorbent in order to examine kinetic of adsorption, influence of pH and effect of common anions present in natural waters.
PB  - Elsevier
T2  - Journal of Saudi Chemical Society
T1  - Microwave-hydrothermal synthesis of TiO2 and zirconium doped TiO2 adsorbents for removal of As(III) and As(V)
VL  - 19
IS  - 4
SP  - 429
EP  - 435
DO  - 10.1016/j.jscs.2014.05.009
ER  - 

@article{
author = "Anđelković, Ivan and Stanković, Dalibor and Jović, Milica and Marković, Marijana and Krstić, Jugoslav and Manojlović, Dragan and Roglić, Goran",
year = "2015",
abstract = "Microwave-hydrothermal method was used for the synthesis of TiO2 and TiO2 doped with zirconium. The method was fast and simple and adsorbents were used for removal of As(III) and As(V) from aqueous solutions. The adsorbents were characterized by BET surface area measurements and powder XRD. Experiments showed that TiO2 doped with 10% of Zr using the microwave-hydrothermal method have greater specific surface area and total pore volume in comparison with TiO2 synthesized using the same method. Better removal with doped adsorbent was obtained for both, As(III) and As(V). Further experiments were carried out with Zr doped TiO2 sorbent in order to examine kinetic of adsorption, influence of pH and effect of common anions present in natural waters.",
publisher = "Elsevier",
journal = "Journal of Saudi Chemical Society",
title = "Microwave-hydrothermal synthesis of TiO2 and zirconium doped TiO2 adsorbents for removal of As(III) and As(V)",
volume = "19",
number = "4",
pages = "429-435",
doi = "10.1016/j.jscs.2014.05.009"
}

Anđelković, I., Stanković, D., Jović, M., Marković, M., Krstić, J., Manojlović, D.,& Roglić, G.. (2015). Microwave-hydrothermal synthesis of TiO2 and zirconium doped TiO2 adsorbents for removal of As(III) and As(V). in Journal of Saudi Chemical Society
Elsevier., 19(4), 429-435.
https://doi.org/10.1016/j.jscs.2014.05.009

Anđelković I, Stanković D, Jović M, Marković M, Krstić J, Manojlović D, Roglić G. Microwave-hydrothermal synthesis of TiO2 and zirconium doped TiO2 adsorbents for removal of As(III) and As(V). in Journal of Saudi Chemical Society. 2015;19(4):429-435.
doi:10.1016/j.jscs.2014.05.009 .

Anđelković, Ivan, Stanković, Dalibor, Jović, Milica, Marković, Marijana, Krstić, Jugoslav, Manojlović, Dragan, Roglić, Goran, "Microwave-hydrothermal synthesis of TiO2 and zirconium doped TiO2 adsorbents for removal of As(III) and As(V)" in Journal of Saudi Chemical Society, 19, no. 4 (2015):429-435,
https://doi.org/10.1016/j.jscs.2014.05.009 . .

TY  - JOUR
AU  - Marković, Marijana
AU  - Jović, Milica
AU  - Stanković, Dalibor
AU  - Kovačević, Vesna V.
AU  - Roglić, Goran
AU  - Gojgić-Cvijović, Gordana
AU  - Manojlović, Dragan
PY  - 2015
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1747
AB  - Pharmaceutical compounds have been detected frequently in surface and ground water. Advanced Oxidation Processes (AOPs) were reported as very efficient for removal of various organic compounds. Nevertheless, due to incomplete degradation, toxic intermediates can induce more severe effects than the parent compound. Therefore, toxicity studies are necessary for the evaluation of possible uses of AOPs. In this study the effectiveness and capacity for environmental application of three different AOPs were estimated. They were applied and evaluated for removal of ibuprofen from water solutions. Therefore, two treatments were performed in a non-thermal plasma reactor with dielectric barrier discharge with and without a homogenous catalyst (Fe2+). The third treatment was the Fenton reaction. The degradation rate of ibuprofen was measured by HPLC-DAD and the main degradation products were identified using LC-MS TOF. Twelve degradation products were identified, and there were differences according to the various treatments applied. Toxicity effects were determined with two bioassays: Vibrio fischeri and Artemia salina. The efficiency of AOPs was demonstrated for all treatments, where after 15 min degradation percentage was over 80% accompanied by opening of the aromatic ring. In the treatment with homogenous catalyst degradation reached 99%. V. fischeri toxicity test has shown greater sensitivity to ibuprofen solution after the Fenton treatment in comparison to A. salina.
PB  - Elsevier
T2  - Science of the Total Environment
T1  - Application of non-thermal plasma reactor and Fenton reaction for degradation of ibuprofen
VL  - 505
SP  - 1148
EP  - 1155
DO  - 10.1016/j.scitotenv.2014.11.017
ER  - 

@article{
author = "Marković, Marijana and Jović, Milica and Stanković, Dalibor and Kovačević, Vesna V. and Roglić, Goran and Gojgić-Cvijović, Gordana and Manojlović, Dragan",
year = "2015",
abstract = "Pharmaceutical compounds have been detected frequently in surface and ground water. Advanced Oxidation Processes (AOPs) were reported as very efficient for removal of various organic compounds. Nevertheless, due to incomplete degradation, toxic intermediates can induce more severe effects than the parent compound. Therefore, toxicity studies are necessary for the evaluation of possible uses of AOPs. In this study the effectiveness and capacity for environmental application of three different AOPs were estimated. They were applied and evaluated for removal of ibuprofen from water solutions. Therefore, two treatments were performed in a non-thermal plasma reactor with dielectric barrier discharge with and without a homogenous catalyst (Fe2+). The third treatment was the Fenton reaction. The degradation rate of ibuprofen was measured by HPLC-DAD and the main degradation products were identified using LC-MS TOF. Twelve degradation products were identified, and there were differences according to the various treatments applied. Toxicity effects were determined with two bioassays: Vibrio fischeri and Artemia salina. The efficiency of AOPs was demonstrated for all treatments, where after 15 min degradation percentage was over 80% accompanied by opening of the aromatic ring. In the treatment with homogenous catalyst degradation reached 99%. V. fischeri toxicity test has shown greater sensitivity to ibuprofen solution after the Fenton treatment in comparison to A. salina.",
publisher = "Elsevier",
journal = "Science of the Total Environment",
title = "Application of non-thermal plasma reactor and Fenton reaction for degradation of ibuprofen",
volume = "505",
pages = "1148-1155",
doi = "10.1016/j.scitotenv.2014.11.017"
}

Marković, M., Jović, M., Stanković, D., Kovačević, V. V., Roglić, G., Gojgić-Cvijović, G.,& Manojlović, D.. (2015). Application of non-thermal plasma reactor and Fenton reaction for degradation of ibuprofen. in Science of the Total Environment
Elsevier., 505, 1148-1155.
https://doi.org/10.1016/j.scitotenv.2014.11.017

Marković M, Jović M, Stanković D, Kovačević VV, Roglić G, Gojgić-Cvijović G, Manojlović D. Application of non-thermal plasma reactor and Fenton reaction for degradation of ibuprofen. in Science of the Total Environment. 2015;505:1148-1155.
doi:10.1016/j.scitotenv.2014.11.017 .

Marković, Marijana, Jović, Milica, Stanković, Dalibor, Kovačević, Vesna V., Roglić, Goran, Gojgić-Cvijović, Gordana, Manojlović, Dragan, "Application of non-thermal plasma reactor and Fenton reaction for degradation of ibuprofen" in Science of the Total Environment, 505 (2015):1148-1155,
https://doi.org/10.1016/j.scitotenv.2014.11.017 . .

TY  - JOUR
AU  - Nesic, Jelena
AU  - Manojlović, Dragan
AU  - Jović, Milica
AU  - Dojčinović, Biljana
AU  - Vulić, Predrag
AU  - Krstić, Jugoslav
AU  - Roglić, Goran
PY  - 2014
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1421
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 >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
ER  - 

@article{
author = "Nesic, Jelena and Manojlović, Dragan and Jović, Milica and Dojčinović, Biljana and Vulić, Predrag and Krstić, 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 >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"
}

Nesic, J., Manojlović, D., Jović, M., Dojčinović, B., Vulić, P., Krstić, 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

Nesic J, Manojlović D, Jović M, Dojčinović B, Vulić P, Krstić 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 .

Nesic, Jelena, Manojlović, Dragan, Jović, Milica, Dojčinović, Biljana, Vulić, Predrag, Krstić, 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 . .

TY  - JOUR
AU  - Marković, Marijana
AU  - Jović, Milica
AU  - Stanković, Dalibor
AU  - Mutić, Jelena
AU  - Roglić, Goran
AU  - Manojlović, Dragan
PY  - 2014
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1481
AB  - The application of various electrodes for in situ degradation of Reactive Yellow 125 (RY125) and Reactive Green 15 (RG15) dyes, as well as ecotoxicity screening test of their degradation products were studied in this paper. The degradation process was performed in a two-electrode cylindrical cell, with Fisher platinum electrode as anode and Pd, Zr, or C electrodes as cathode; in 0.1 M Na2SO4 as supporting electrolyte. The optimal conditions (voltage and pH value) for degradation were determined in a platinum-palladium (Pt-Pd) model system for 200 mg/L of both reactive dyes. Then the electrolysis with other electrodes was conducted under the same conditions. Decolorization was monitored spectrofotometrically (UV-Vis) and the degradation efficiency was confirmed by HPLC technique with a DAD detector. Differences in degradation efficiency were observed between these three electrochemical systems (Pt-Pd, Pt-Zr, and Pt-C). The Pt-Pd system was the most efficient for the degradation of both reactive dyes. Achieved decolorization percentage for RG15 and RY125 were 98% and 97%, respectively. The ecotoxicity assessment of degradation products was performed using Anemia sauna. Toxicity data were compared by Kruskal-Wallis one-way analysis and pair-wise group comparisons with Mann-Whitney U tests. Statistically significant differences (p LT 0.05) in mortality (%) for Pt-Pd and Pt-Zr systems were determined between treated and untreated dye solutions of RG15. System Pt-C had no detectable significance in treatment of solutions of both dyes.
PB  - Hard, Olsztyn 5
T2  - Polish Journal of Environmental Studies
T1  - Toxicity Screening after Electrochemical Degradation of Reactive Textile Dyes
VL  - 23
IS  - 6
SP  - 2103
EP  - 2109
DO  - 10.15244/pjoes/28298
ER  - 

@article{
author = "Marković, Marijana and Jović, Milica and Stanković, Dalibor and Mutić, Jelena and Roglić, Goran and Manojlović, Dragan",
year = "2014",
abstract = "The application of various electrodes for in situ degradation of Reactive Yellow 125 (RY125) and Reactive Green 15 (RG15) dyes, as well as ecotoxicity screening test of their degradation products were studied in this paper. The degradation process was performed in a two-electrode cylindrical cell, with Fisher platinum electrode as anode and Pd, Zr, or C electrodes as cathode; in 0.1 M Na2SO4 as supporting electrolyte. The optimal conditions (voltage and pH value) for degradation were determined in a platinum-palladium (Pt-Pd) model system for 200 mg/L of both reactive dyes. Then the electrolysis with other electrodes was conducted under the same conditions. Decolorization was monitored spectrofotometrically (UV-Vis) and the degradation efficiency was confirmed by HPLC technique with a DAD detector. Differences in degradation efficiency were observed between these three electrochemical systems (Pt-Pd, Pt-Zr, and Pt-C). The Pt-Pd system was the most efficient for the degradation of both reactive dyes. Achieved decolorization percentage for RG15 and RY125 were 98% and 97%, respectively. The ecotoxicity assessment of degradation products was performed using Anemia sauna. Toxicity data were compared by Kruskal-Wallis one-way analysis and pair-wise group comparisons with Mann-Whitney U tests. Statistically significant differences (p LT 0.05) in mortality (%) for Pt-Pd and Pt-Zr systems were determined between treated and untreated dye solutions of RG15. System Pt-C had no detectable significance in treatment of solutions of both dyes.",
publisher = "Hard, Olsztyn 5",
journal = "Polish Journal of Environmental Studies",
title = "Toxicity Screening after Electrochemical Degradation of Reactive Textile Dyes",
volume = "23",
number = "6",
pages = "2103-2109",
doi = "10.15244/pjoes/28298"
}

Marković, M., Jović, M., Stanković, D., Mutić, J., Roglić, G.,& Manojlović, D.. (2014). Toxicity Screening after Electrochemical Degradation of Reactive Textile Dyes. in Polish Journal of Environmental Studies
Hard, Olsztyn 5., 23(6), 2103-2109.
https://doi.org/10.15244/pjoes/28298

Marković M, Jović M, Stanković D, Mutić J, Roglić G, Manojlović D. Toxicity Screening after Electrochemical Degradation of Reactive Textile Dyes. in Polish Journal of Environmental Studies. 2014;23(6):2103-2109.
doi:10.15244/pjoes/28298 .

Marković, Marijana, Jović, Milica, Stanković, Dalibor, Mutić, Jelena, Roglić, Goran, Manojlović, Dragan, "Toxicity Screening after Electrochemical Degradation of Reactive Textile Dyes" in Polish Journal of Environmental Studies, 23, no. 6 (2014):2103-2109,
https://doi.org/10.15244/pjoes/28298 . .

TY  - JOUR
AU  - Jović, Milica
AU  - Manojlović, Dragan
AU  - Stanković, Dalibor
AU  - Marković, Marijana
AU  - Anđelković, Ivan
AU  - Papan, Jelena
AU  - Roglić, Goran
PY  - 2014
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1544
AB  - Electrochemical treatment is a new trend for the purification of textile industry wastewater which containing azo dyes. In this paper the electrochemical treatment was used for decolorization of azo dye Reactive Blue 52. The efficiency of decolorization was compared for different electrochemical systems which were all equipped with Fisher platinum electrode as anode and a different cathode (Zr, Pd, C) in sodium sulfate as supporting electrolyte. In order to find optimal conditions the influence of various voltage and pH values of initial dye solution was studied. Decolorization rate was monitored by spectrophotometer while degradation products were identified by high performance liquid chromatography-diode array detector (HPLC-DAD). Results of HPLC analysis confirmed presence of various degradation products in electrochemical systems, which indicated different mechanism of degradation. This was also confirmed by Ek-t curve. In terms of power consumption the most cost effective system was with the graphite cathode (C/Pt).
PB  - Wiley-Blackwell, Hoboken
T2  - Clean-Soil Air Water
T1  - Electrochemical Treatment of Reactive Blue 52 Using Zirconium, Palladium and Graphite Electrode
VL  - 42
IS  - 6
SP  - 804
EP  - 808
DO  - 10.1002/clen.201300245
ER  - 

@article{
author = "Jović, Milica and Manojlović, Dragan and Stanković, Dalibor and Marković, Marijana and Anđelković, Ivan and Papan, Jelena and Roglić, Goran",
year = "2014",
abstract = "Electrochemical treatment is a new trend for the purification of textile industry wastewater which containing azo dyes. In this paper the electrochemical treatment was used for decolorization of azo dye Reactive Blue 52. The efficiency of decolorization was compared for different electrochemical systems which were all equipped with Fisher platinum electrode as anode and a different cathode (Zr, Pd, C) in sodium sulfate as supporting electrolyte. In order to find optimal conditions the influence of various voltage and pH values of initial dye solution was studied. Decolorization rate was monitored by spectrophotometer while degradation products were identified by high performance liquid chromatography-diode array detector (HPLC-DAD). Results of HPLC analysis confirmed presence of various degradation products in electrochemical systems, which indicated different mechanism of degradation. This was also confirmed by Ek-t curve. In terms of power consumption the most cost effective system was with the graphite cathode (C/Pt).",
publisher = "Wiley-Blackwell, Hoboken",
journal = "Clean-Soil Air Water",
title = "Electrochemical Treatment of Reactive Blue 52 Using Zirconium, Palladium and Graphite Electrode",
volume = "42",
number = "6",
pages = "804-808",
doi = "10.1002/clen.201300245"
}

Jović, M., Manojlović, D., Stanković, D., Marković, M., Anđelković, I., Papan, J.,& Roglić, G.. (2014). Electrochemical Treatment of Reactive Blue 52 Using Zirconium, Palladium and Graphite Electrode. in Clean-Soil Air Water
Wiley-Blackwell, Hoboken., 42(6), 804-808.
https://doi.org/10.1002/clen.201300245

Jović M, Manojlović D, Stanković D, Marković M, Anđelković I, Papan J, Roglić G. Electrochemical Treatment of Reactive Blue 52 Using Zirconium, Palladium and Graphite Electrode. in Clean-Soil Air Water. 2014;42(6):804-808.
doi:10.1002/clen.201300245 .

Jović, Milica, Manojlović, Dragan, Stanković, Dalibor, Marković, Marijana, Anđelković, Ivan, Papan, Jelena, Roglić, Goran, "Electrochemical Treatment of Reactive Blue 52 Using Zirconium, Palladium and Graphite Electrode" in Clean-Soil Air Water, 42, no. 6 (2014):804-808,
https://doi.org/10.1002/clen.201300245 . .

TY  - JOUR
AU  - Jović, Milica
AU  - Dojčinović, Biljana
AU  - Kovačević, Vesna V.
AU  - Obradović, Bratislav M.
AU  - Kuraica, Milorad M.
AU  - Gašić, Uroš
AU  - Roglić, Goran
PY  - 2014
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1590
AB  - In this study the effect of different homogenous catalysts and their dosage on mesotrione degradation in water falling film dielectric barrier discharge (DBD) reactor was investigated. Four catalytic systems Mn2+ /DBD, Co2+/DBD, Fe2+/DBD and H2O2/DBD were examined. In order to find optimal conditions various concentrations of catalysts and specific energy density (SED) values were tested in each system. Mesotrione degradation efficiency was determined by HPLC-DAD and mineralization efficiency by TOC value. Degradation products were identified by UHPLC-Orbitrap-MS and compared after finding out the optimal concentration for each catalytic system. All studied catalytic systems have proved to be successful in improving mesotrione removal, but the highest improvement in degradation efficiency was obtained with catalytic system 5 ppm Fe2+/DBD (by 50% for SED 124 kJ/L) and 10 mM H2O2/DBD for improving mineralization efficiency (by 45% for SED 310 kJ/L). Nine degradation products were identified in catalytic DBD treatments. Main degradation products were: glutaric acid, 2-nitro-4-methylsulfonylbenzaldehyde and 2-nitro-4-methylsulfonylbenzoic acid. H2O2/DBD gave significantly different degradation products than other catalytic systems. Dominant degradation products in other systems were not identified in system with hydrogen peroxide, which supported the fact that the highest mineralization efficiency was achieved with peroxide catalytic system. Global toxicity of samples after degradation in each system was determined using Artemia sauna and they could be considered as "non toxic".
PB  - Elsevier Science Sa, Lausanne
T2  - Chemical Engineering Journal
T1  - Effect of different catalysts on mesotrione degradation in water falling film DBD reactor
VL  - 248
SP  - 63
EP  - 70
DO  - 10.1016/j.cej.2014.03.031
ER  - 

@article{
author = "Jović, Milica and Dojčinović, Biljana and Kovačević, Vesna V. and Obradović, Bratislav M. and Kuraica, Milorad M. and Gašić, Uroš and Roglić, Goran",
year = "2014",
abstract = "In this study the effect of different homogenous catalysts and their dosage on mesotrione degradation in water falling film dielectric barrier discharge (DBD) reactor was investigated. Four catalytic systems Mn2+ /DBD, Co2+/DBD, Fe2+/DBD and H2O2/DBD were examined. In order to find optimal conditions various concentrations of catalysts and specific energy density (SED) values were tested in each system. Mesotrione degradation efficiency was determined by HPLC-DAD and mineralization efficiency by TOC value. Degradation products were identified by UHPLC-Orbitrap-MS and compared after finding out the optimal concentration for each catalytic system. All studied catalytic systems have proved to be successful in improving mesotrione removal, but the highest improvement in degradation efficiency was obtained with catalytic system 5 ppm Fe2+/DBD (by 50% for SED 124 kJ/L) and 10 mM H2O2/DBD for improving mineralization efficiency (by 45% for SED 310 kJ/L). Nine degradation products were identified in catalytic DBD treatments. Main degradation products were: glutaric acid, 2-nitro-4-methylsulfonylbenzaldehyde and 2-nitro-4-methylsulfonylbenzoic acid. H2O2/DBD gave significantly different degradation products than other catalytic systems. Dominant degradation products in other systems were not identified in system with hydrogen peroxide, which supported the fact that the highest mineralization efficiency was achieved with peroxide catalytic system. Global toxicity of samples after degradation in each system was determined using Artemia sauna and they could be considered as "non toxic".",
publisher = "Elsevier Science Sa, Lausanne",
journal = "Chemical Engineering Journal",
title = "Effect of different catalysts on mesotrione degradation in water falling film DBD reactor",
volume = "248",
pages = "63-70",
doi = "10.1016/j.cej.2014.03.031"
}

Jović, M., Dojčinović, B., Kovačević, V. V., Obradović, B. M., Kuraica, M. M., Gašić, U.,& Roglić, G.. (2014). Effect of different catalysts on mesotrione degradation in water falling film DBD reactor. in Chemical Engineering Journal
Elsevier Science Sa, Lausanne., 248, 63-70.
https://doi.org/10.1016/j.cej.2014.03.031

Jović M, Dojčinović B, Kovačević VV, Obradović BM, Kuraica MM, Gašić U, Roglić G. Effect of different catalysts on mesotrione degradation in water falling film DBD reactor. in Chemical Engineering Journal. 2014;248:63-70.
doi:10.1016/j.cej.2014.03.031 .

Jović, Milica, Dojčinović, Biljana, Kovačević, Vesna V., Obradović, Bratislav M., Kuraica, Milorad M., Gašić, Uroš, Roglić, Goran, "Effect of different catalysts on mesotrione degradation in water falling film DBD reactor" in Chemical Engineering Journal, 248 (2014):63-70,
https://doi.org/10.1016/j.cej.2014.03.031 . .

TY  - JOUR
AU  - Jović, Milica
AU  - Stanković, Dalibor
AU  - Manojlović, Dragan
AU  - Anđelković, Ivan
AU  - Milic, Andelija
AU  - Dojčinović, Biljana
AU  - Roglić, Goran
PY  - 2013
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1351
AB  - Textile industries are widespread in developing countries. Among the various processes in the textile industry, the dyeing process uses large volumes of water for dyeing, fixing and washing. Textile industry wastewater is characterized by intensive color and high chemical oxygen demand (COD) concentrations that discarding of these toxic wastewaters to the environment will cause a major problem. In this study electrochemical oxidation of reactive textile dyes: Reactive Blue 52, Reactive Black 5, Reactive Green 15, and Reactive Yellow 125, using platinum anode was examined. Electrolysis is carried out in electrochemical cell containing membrane which is standard membrane in industry. Membrane separated anodic and cathodic area. Supporting electrolyte was 0.1M sodium sulfate which is also present in real textile effluents. Applied voltage of 6, 12 and 24V, and influence of membrane on electrolysis were examined on model dye (Reactive Blue 52). Highest degradation degree for model dye was achieved at 12V, so electrolysis of other dyes was done on this voltage. COD value of all dyes dropped after 60 minutes of electrolysis below a measurable level ( LT 30mg/L O-2), except Reactive Black 5 whose COD reduction was 57.95% with membrane and 35.28% without membrane applied. Complete decolorization was achieved after 10 to 60 minutes for all dyes. Degradation products of model dye Reactive Blue 52 were monitored with HPLC, and influence of pH on decolorization was also examined on model dye.
PB  - Esg, Belgrade
T2  - International Journal of Electrochemical Science
T1  - Study of the Electrochemical Oxidation of Reactive Textile Dyes Using Platinum Electrode
VL  - 8
IS  - 1
SP  - 168
EP  - 183
UR  - https://hdl.handle.net/21.15107/rcub_cherry_1615
ER  - 

@article{
author = "Jović, Milica and Stanković, Dalibor and Manojlović, Dragan and Anđelković, Ivan and Milic, Andelija and Dojčinović, Biljana and Roglić, Goran",
year = "2013",
abstract = "Textile industries are widespread in developing countries. Among the various processes in the textile industry, the dyeing process uses large volumes of water for dyeing, fixing and washing. Textile industry wastewater is characterized by intensive color and high chemical oxygen demand (COD) concentrations that discarding of these toxic wastewaters to the environment will cause a major problem. In this study electrochemical oxidation of reactive textile dyes: Reactive Blue 52, Reactive Black 5, Reactive Green 15, and Reactive Yellow 125, using platinum anode was examined. Electrolysis is carried out in electrochemical cell containing membrane which is standard membrane in industry. Membrane separated anodic and cathodic area. Supporting electrolyte was 0.1M sodium sulfate which is also present in real textile effluents. Applied voltage of 6, 12 and 24V, and influence of membrane on electrolysis were examined on model dye (Reactive Blue 52). Highest degradation degree for model dye was achieved at 12V, so electrolysis of other dyes was done on this voltage. COD value of all dyes dropped after 60 minutes of electrolysis below a measurable level ( LT 30mg/L O-2), except Reactive Black 5 whose COD reduction was 57.95% with membrane and 35.28% without membrane applied. Complete decolorization was achieved after 10 to 60 minutes for all dyes. Degradation products of model dye Reactive Blue 52 were monitored with HPLC, and influence of pH on decolorization was also examined on model dye.",
publisher = "Esg, Belgrade",
journal = "International Journal of Electrochemical Science",
title = "Study of the Electrochemical Oxidation of Reactive Textile Dyes Using Platinum Electrode",
volume = "8",
number = "1",
pages = "168-183",
url = "https://hdl.handle.net/21.15107/rcub_cherry_1615"
}

Jović, M., Stanković, D., Manojlović, D., Anđelković, I., Milic, A., Dojčinović, B.,& Roglić, G.. (2013). Study of the Electrochemical Oxidation of Reactive Textile Dyes Using Platinum Electrode. in International Journal of Electrochemical Science
Esg, Belgrade., 8(1), 168-183.
https://hdl.handle.net/21.15107/rcub_cherry_1615

Jović M, Stanković D, Manojlović D, Anđelković I, Milic A, Dojčinović B, Roglić G. Study of the Electrochemical Oxidation of Reactive Textile Dyes Using Platinum Electrode. in International Journal of Electrochemical Science. 2013;8(1):168-183.
https://hdl.handle.net/21.15107/rcub_cherry_1615 .

Jović, Milica, Stanković, Dalibor, Manojlović, Dragan, Anđelković, Ivan, Milic, Andelija, Dojčinović, Biljana, Roglić, Goran, "Study of the Electrochemical Oxidation of Reactive Textile Dyes Using Platinum Electrode" in International Journal of Electrochemical Science, 8, no. 1 (2013):168-183,
https://hdl.handle.net/21.15107/rcub_cherry_1615 .

TY  - JOUR
AU  - Jović, Milica
AU  - Manojlović, Dragan
AU  - Stanković, Dalibor
AU  - Dojčinović, Biljana
AU  - Obradović, Bratislav M.
AU  - Gašić, Uroš
AU  - Roglić, Goran
PY  - 2013
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1185
AB  - Degradation of two triketone herbicides, mesotrione and sulcotrione, was studied using four different advanced oxidation processes (AOPs): ozonization, dielectric barrier discharge (DBD reactor), photocatalysis and Fenton reagent, in order to find differences in mechanism of degradation. Degradation products were identified by high performance liquid chromatography (HPLC-DAD) and UHPLC-Orbitrap-MS analyses. A simple mechanism of degradation for different AOP was proposed. Thirteen products were identified during all degradations for both pesticides. It was assumed that the oxidation mechanisms in the all four technologies were not based only on the production and use of the hydroxyl radical, but they also included other kinds of oxidation mechanisms specific for each technology. Similarity was observed between degradation mechanism of ozonation and DBD. The greatest difference in the products was found in Fenton degradation which included the opening of benzene ring. When degraded with same AOP pesticides gave at the end of treatment the same products. Global toxicity and COD value of samples was determined after all degradations. Real water sample was used to study influence of organic matter on pesticide degradation. These results could lead to accurate estimates of the overall effects of triketone herbicides on environmental ecosystems and also contributed to the development of improved removal processes.
PB  - Elsevier
T2  - Journal of Hazardous Materials
T1  - Degradation of triketone herbicides, mesotrione and sulcotrione, using advanced oxidation processes
VL  - 260
SP  - 1092
EP  - 1099
DO  - 10.1016/j.jhazmat.2013.06.073
ER  - 

@article{
author = "Jović, Milica and Manojlović, Dragan and Stanković, Dalibor and Dojčinović, Biljana and Obradović, Bratislav M. and Gašić, Uroš and Roglić, Goran",
year = "2013",
abstract = "Degradation of two triketone herbicides, mesotrione and sulcotrione, was studied using four different advanced oxidation processes (AOPs): ozonization, dielectric barrier discharge (DBD reactor), photocatalysis and Fenton reagent, in order to find differences in mechanism of degradation. Degradation products were identified by high performance liquid chromatography (HPLC-DAD) and UHPLC-Orbitrap-MS analyses. A simple mechanism of degradation for different AOP was proposed. Thirteen products were identified during all degradations for both pesticides. It was assumed that the oxidation mechanisms in the all four technologies were not based only on the production and use of the hydroxyl radical, but they also included other kinds of oxidation mechanisms specific for each technology. Similarity was observed between degradation mechanism of ozonation and DBD. The greatest difference in the products was found in Fenton degradation which included the opening of benzene ring. When degraded with same AOP pesticides gave at the end of treatment the same products. Global toxicity and COD value of samples was determined after all degradations. Real water sample was used to study influence of organic matter on pesticide degradation. These results could lead to accurate estimates of the overall effects of triketone herbicides on environmental ecosystems and also contributed to the development of improved removal processes.",
publisher = "Elsevier",
journal = "Journal of Hazardous Materials",
title = "Degradation of triketone herbicides, mesotrione and sulcotrione, using advanced oxidation processes",
volume = "260",
pages = "1092-1099",
doi = "10.1016/j.jhazmat.2013.06.073"
}

Jović, M., Manojlović, D., Stanković, D., Dojčinović, B., Obradović, B. M., Gašić, U.,& Roglić, G.. (2013). Degradation of triketone herbicides, mesotrione and sulcotrione, using advanced oxidation processes. in Journal of Hazardous Materials
Elsevier., 260, 1092-1099.
https://doi.org/10.1016/j.jhazmat.2013.06.073

Jović M, Manojlović D, Stanković D, Dojčinović B, Obradović BM, Gašić U, Roglić G. Degradation of triketone herbicides, mesotrione and sulcotrione, using advanced oxidation processes. in Journal of Hazardous Materials. 2013;260:1092-1099.
doi:10.1016/j.jhazmat.2013.06.073 .

Jović, Milica, Manojlović, Dragan, Stanković, Dalibor, Dojčinović, Biljana, Obradović, Bratislav M., Gašić, Uroš, Roglić, Goran, "Degradation of triketone herbicides, mesotrione and sulcotrione, using advanced oxidation processes" in Journal of Hazardous Materials, 260 (2013):1092-1099,
https://doi.org/10.1016/j.jhazmat.2013.06.073 . .