Dugandžić, Ana M.

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  • Dugandžić, Ana M. (4)
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Author's Bibliography

Degradation of nicosulfuron using fenton and fenton-like reactions

Dugandžić, Ana M.; Tomašević, Anđelka; Dabić, Dunja M.; Šekuljica, Nataša; Radišić, Marina; Petrović, Slobodan; Mijin, Dušan

(Savez hemijskih inženjera, Beograd, 2018)

TY  - JOUR
AU  - Dugandžić, Ana M.
AU  - Tomašević, Anđelka
AU  - Dabić, Dunja M.
AU  - Šekuljica, Nataša
AU  - Radišić, Marina
AU  - Petrović, Slobodan
AU  - Mijin, Dušan
PY  - 2018
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3892
AB  - Nicosulfuron, a sulfonylurea herbicide, was subjected to different Fenton reactions at pH of a nicosulfuron aqueous solution (pH 5). Usually, the optimal pH for the Fenton reaction is between 3 and 4, but the addition of acids is not environmentally acceptable. This is the reason why the reactions were performed at a higher pH value than usual. So, classical Fenton and Fenton-like reactions were applied as well as phot-Fenton and photo-Fenton-like reactions. In addition, microwave Fenton and Fenton-like reactions were used in nicosulfuron degradation. Influences of Fe2+ and Fe3+ concentrations, as well as hydrogen peroxide concentrations, were studied The Fenton reaction was much faster and more efficient than the Fenton-like reaction, while the photo-Fenton reaction proceeded much faster and more efficiently than the Fenton reaction. The microwave-Fenton and microwave-Fenton-like reactions proceeded with increased efficiency in comparison to the Fenton and Fenton-like reactions. The phytotoxicity and acute toxicity of the reaction products of nicosulfuron oxidation by the photo-Fenton reaction were analyzed The toxicity testing of nicosulfuron treatment by photo-Fenton process showed a decrease in phytotoxicity, while the acute toxicity tests showed that the samples after treatment had lower toxicity.
PB  - Savez hemijskih inženjera, Beograd
T2  - Chemical Industry & Chemical Engineering Quarterly
T1  - Degradation of nicosulfuron using fenton and fenton-like reactions
EP  - 208
IS  - 3
SP  - 201
VL  - 24
DO  - 10.2298/CICEQ170617032D
ER  - 
@article{
author = "Dugandžić, Ana M. and Tomašević, Anđelka and Dabić, Dunja M. and Šekuljica, Nataša and Radišić, Marina and Petrović, Slobodan and Mijin, Dušan",
year = "2018",
abstract = "Nicosulfuron, a sulfonylurea herbicide, was subjected to different Fenton reactions at pH of a nicosulfuron aqueous solution (pH 5). Usually, the optimal pH for the Fenton reaction is between 3 and 4, but the addition of acids is not environmentally acceptable. This is the reason why the reactions were performed at a higher pH value than usual. So, classical Fenton and Fenton-like reactions were applied as well as phot-Fenton and photo-Fenton-like reactions. In addition, microwave Fenton and Fenton-like reactions were used in nicosulfuron degradation. Influences of Fe2+ and Fe3+ concentrations, as well as hydrogen peroxide concentrations, were studied The Fenton reaction was much faster and more efficient than the Fenton-like reaction, while the photo-Fenton reaction proceeded much faster and more efficiently than the Fenton reaction. The microwave-Fenton and microwave-Fenton-like reactions proceeded with increased efficiency in comparison to the Fenton and Fenton-like reactions. The phytotoxicity and acute toxicity of the reaction products of nicosulfuron oxidation by the photo-Fenton reaction were analyzed The toxicity testing of nicosulfuron treatment by photo-Fenton process showed a decrease in phytotoxicity, while the acute toxicity tests showed that the samples after treatment had lower toxicity.",
publisher = "Savez hemijskih inženjera, Beograd",
journal = "Chemical Industry & Chemical Engineering Quarterly",
title = "Degradation of nicosulfuron using fenton and fenton-like reactions",
pages = "208-201",
number = "3",
volume = "24",
doi = "10.2298/CICEQ170617032D"
}
Dugandžić, A. M., Tomašević, A., Dabić, D. M., Šekuljica, N., Radišić, M., Petrović, S.,& Mijin, D.. (2018). Degradation of nicosulfuron using fenton and fenton-like reactions. in Chemical Industry & Chemical Engineering Quarterly
Savez hemijskih inženjera, Beograd., 24(3), 201-208.
https://doi.org/10.2298/CICEQ170617032D
Dugandžić AM, Tomašević A, Dabić DM, Šekuljica N, Radišić M, Petrović S, Mijin D. Degradation of nicosulfuron using fenton and fenton-like reactions. in Chemical Industry & Chemical Engineering Quarterly. 2018;24(3):201-208.
doi:10.2298/CICEQ170617032D .
Dugandžić, Ana M., Tomašević, Anđelka, Dabić, Dunja M., Šekuljica, Nataša, Radišić, Marina, Petrović, Slobodan, Mijin, Dušan, "Degradation of nicosulfuron using fenton and fenton-like reactions" in Chemical Industry & Chemical Engineering Quarterly, 24, no. 3 (2018):201-208,
https://doi.org/10.2298/CICEQ170617032D . .
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Effect of inorganic ions, photosensitisers and scavengers on the photocatalytic degradation of nicosulfuron

Dugandžić, Ana M.; Tomašević, Anđelka; Radišić, Marina; Šekuljica, Nataša; Mijin, Dušan; Petrović, Slobodan

(Elsevier Science Sa, Lausanne, 2017)

TY  - JOUR
AU  - Dugandžić, Ana M.
AU  - Tomašević, Anđelka
AU  - Radišić, Marina
AU  - Šekuljica, Nataša
AU  - Mijin, Dušan
AU  - Petrović, Slobodan
PY  - 2017
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3701
AB  - In the present study, the photocatalytic degradation of nicosulfuron, using TiO2 as a catalyst under UV light (315-400 nm), was studied. The optimization of the nicosulfuron photodegradation was performed. It was found that the optimal concentration of the catalyst was 1 g L-1 at concentration of nicosulfuron solution of 20 mg L-1 while the highest reaction rate was obtained using 2 g L-1. The degradation rate was the highest at pH .= 5.0. Effects of anions (Cl-, SO42- NO3- and F-) and cations (Na+, Ca2+, Al3+) were investigated. In addition, the influence of isopropanol, acetone, and hydrogen peroxide was studied. It was shown that the photocatalytic degradation is mainly due to the reaction of nicosulfuron with (OH)-O-center dot in solution. Also, liquid chromatography coupled with mass spectrometry (HPLC-MS) was used to identify intermediates during the photocatalytic degradation of nicosulfuron. the mineralization was monitored with ion chromatography (IC) and total organic carbon (TOC) analysis. Although 100% HPLC removal of nicosulfuron was achieved, only 69% TOC removal after 90 min was recorded. The results of ion chromatography showed that the mineralization resulted in ammonium and nitrate ions during the process. The phytotoxicity experiments using mung bean seeds showed a reduction in phytotoxicity.
PB  - Elsevier Science Sa, Lausanne
T2  - Journal of Photochemistry and Photobiology A-Chemistry
T1  - Effect of inorganic ions, photosensitisers and scavengers on the photocatalytic degradation of nicosulfuron
EP  - 155
SP  - 146
VL  - 336
DO  - 10.1016/j.jphotochem.2016.12.031
ER  - 
@article{
author = "Dugandžić, Ana M. and Tomašević, Anđelka and Radišić, Marina and Šekuljica, Nataša and Mijin, Dušan and Petrović, Slobodan",
year = "2017",
abstract = "In the present study, the photocatalytic degradation of nicosulfuron, using TiO2 as a catalyst under UV light (315-400 nm), was studied. The optimization of the nicosulfuron photodegradation was performed. It was found that the optimal concentration of the catalyst was 1 g L-1 at concentration of nicosulfuron solution of 20 mg L-1 while the highest reaction rate was obtained using 2 g L-1. The degradation rate was the highest at pH .= 5.0. Effects of anions (Cl-, SO42- NO3- and F-) and cations (Na+, Ca2+, Al3+) were investigated. In addition, the influence of isopropanol, acetone, and hydrogen peroxide was studied. It was shown that the photocatalytic degradation is mainly due to the reaction of nicosulfuron with (OH)-O-center dot in solution. Also, liquid chromatography coupled with mass spectrometry (HPLC-MS) was used to identify intermediates during the photocatalytic degradation of nicosulfuron. the mineralization was monitored with ion chromatography (IC) and total organic carbon (TOC) analysis. Although 100% HPLC removal of nicosulfuron was achieved, only 69% TOC removal after 90 min was recorded. The results of ion chromatography showed that the mineralization resulted in ammonium and nitrate ions during the process. The phytotoxicity experiments using mung bean seeds showed a reduction in phytotoxicity.",
publisher = "Elsevier Science Sa, Lausanne",
journal = "Journal of Photochemistry and Photobiology A-Chemistry",
title = "Effect of inorganic ions, photosensitisers and scavengers on the photocatalytic degradation of nicosulfuron",
pages = "155-146",
volume = "336",
doi = "10.1016/j.jphotochem.2016.12.031"
}
Dugandžić, A. M., Tomašević, A., Radišić, M., Šekuljica, N., Mijin, D.,& Petrović, S.. (2017). Effect of inorganic ions, photosensitisers and scavengers on the photocatalytic degradation of nicosulfuron. in Journal of Photochemistry and Photobiology A-Chemistry
Elsevier Science Sa, Lausanne., 336, 146-155.
https://doi.org/10.1016/j.jphotochem.2016.12.031
Dugandžić AM, Tomašević A, Radišić M, Šekuljica N, Mijin D, Petrović S. Effect of inorganic ions, photosensitisers and scavengers on the photocatalytic degradation of nicosulfuron. in Journal of Photochemistry and Photobiology A-Chemistry. 2017;336:146-155.
doi:10.1016/j.jphotochem.2016.12.031 .
Dugandžić, Ana M., Tomašević, Anđelka, Radišić, Marina, Šekuljica, Nataša, Mijin, Dušan, Petrović, Slobodan, "Effect of inorganic ions, photosensitisers and scavengers on the photocatalytic degradation of nicosulfuron" in Journal of Photochemistry and Photobiology A-Chemistry, 336 (2017):146-155,
https://doi.org/10.1016/j.jphotochem.2016.12.031 . .
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Photodegradation of dimethenamid-p in deionised and ground water

Glavaski, Olivera; Petrović, Slobodan; Rajaković-Ognjanović, Vladana; Zeremski, Tijana; Dugandžić, Ana M.; Mijin, Dušan

(Savez hemijskih inženjera, Beograd, 2016)

TY  - JOUR
AU  - Glavaski, Olivera
AU  - Petrović, Slobodan
AU  - Rajaković-Ognjanović, Vladana
AU  - Zeremski, Tijana
AU  - Dugandžić, Ana M.
AU  - Mijin, Dušan
PY  - 2016
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3459
AB  - The study of photodegradation of dimethenamid-P herbicide was performed in deionised and ground water using TiO2 as a catalyst under UV light. The effect of electron acceptor (H2O2), scavenger of (OH)-O-center dot radicals (C2H5OH) and scavenger of holes (NaCl and Na2SO4) as well as solution pH was analyzed. The photodegradation of dimethenamid-P was followed by HPLC. The formation of transformation products was followed using high performance liquid chromatography-electrospray mass spectrometry. Ion chromatography and total organic carbon measurements were used for the determination of the mineralization level. HPLC analysis showed the almost complete removal of herbicide after 90 min in deionised and ground water, while total organic carbon analysis showed that dimethenamid-P was mineralized 64 and 50% in deionised and ground water, respectively. The ion chromatography results showed that the mineralization process leads to the formation of chloride, sulphate and nitrate anions during the process. Transformation products were identified and the degradation mechanism was proposed.
PB  - Savez hemijskih inženjera, Beograd
T2  - Chemical Industry & Chemical Engineering Quarterly
T1  - Photodegradation of dimethenamid-p in deionised and ground water
EP  - 110
IS  - 1
SP  - 101
VL  - 22
DO  - 10.2298/CICEQ150608025G
ER  - 
@article{
author = "Glavaski, Olivera and Petrović, Slobodan and Rajaković-Ognjanović, Vladana and Zeremski, Tijana and Dugandžić, Ana M. and Mijin, Dušan",
year = "2016",
abstract = "The study of photodegradation of dimethenamid-P herbicide was performed in deionised and ground water using TiO2 as a catalyst under UV light. The effect of electron acceptor (H2O2), scavenger of (OH)-O-center dot radicals (C2H5OH) and scavenger of holes (NaCl and Na2SO4) as well as solution pH was analyzed. The photodegradation of dimethenamid-P was followed by HPLC. The formation of transformation products was followed using high performance liquid chromatography-electrospray mass spectrometry. Ion chromatography and total organic carbon measurements were used for the determination of the mineralization level. HPLC analysis showed the almost complete removal of herbicide after 90 min in deionised and ground water, while total organic carbon analysis showed that dimethenamid-P was mineralized 64 and 50% in deionised and ground water, respectively. The ion chromatography results showed that the mineralization process leads to the formation of chloride, sulphate and nitrate anions during the process. Transformation products were identified and the degradation mechanism was proposed.",
publisher = "Savez hemijskih inženjera, Beograd",
journal = "Chemical Industry & Chemical Engineering Quarterly",
title = "Photodegradation of dimethenamid-p in deionised and ground water",
pages = "110-101",
number = "1",
volume = "22",
doi = "10.2298/CICEQ150608025G"
}
Glavaski, O., Petrović, S., Rajaković-Ognjanović, V., Zeremski, T., Dugandžić, A. M.,& Mijin, D.. (2016). Photodegradation of dimethenamid-p in deionised and ground water. in Chemical Industry & Chemical Engineering Quarterly
Savez hemijskih inženjera, Beograd., 22(1), 101-110.
https://doi.org/10.2298/CICEQ150608025G
Glavaski O, Petrović S, Rajaković-Ognjanović V, Zeremski T, Dugandžić AM, Mijin D. Photodegradation of dimethenamid-p in deionised and ground water. in Chemical Industry & Chemical Engineering Quarterly. 2016;22(1):101-110.
doi:10.2298/CICEQ150608025G .
Glavaski, Olivera, Petrović, Slobodan, Rajaković-Ognjanović, Vladana, Zeremski, Tijana, Dugandžić, Ana M., Mijin, Dušan, "Photodegradation of dimethenamid-p in deionised and ground water" in Chemical Industry & Chemical Engineering Quarterly, 22, no. 1 (2016):101-110,
https://doi.org/10.2298/CICEQ150608025G . .
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Electrochemical Degradation of the Pesticide Dimethenamid-P at Gold, DSA Platinum and Ruthenium Oxide Electrodes in Different Electrolytes

Glavaski, Olivera; Petrović, Slobodan; Mijin, Dušan; Jovanović, Mica B.; Dugandžić, Ana M.; Zeremski, Tijana; Avramov-Ivić, Milka

(Wiley-VCH Verlag Gmbh, Weinheim, 2014)

TY  - JOUR
AU  - Glavaski, Olivera
AU  - Petrović, Slobodan
AU  - Mijin, Dušan
AU  - Jovanović, Mica B.
AU  - Dugandžić, Ana M.
AU  - Zeremski, Tijana
AU  - Avramov-Ivić, Milka
PY  - 2014
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/2743
AB  - For the first time the electrochemical degradation of the pesticide dimethenamid-P was studied. Its direct electrochemical degradation, using potential cycling at a gold electrode, was performed by cyclic voltammetry and HPLC analysis of electrolyte after 72 h showed 56.8% of degradation. HPLC-MS indicates the formation of degradation products through the elimination of chlorine atom and C-N bond cleavage. By indirect electrolysis using DSA Ti/PtOx and DSA Ti/RuO2 electrodes during 30 minutes 87.2% and 88.3% of dimethenamid-P was degradated, respectively. The high percentage of degradation of dimethenamid-P was achieved with non time consuming, simple and cheap electrochemical processes.
PB  - Wiley-VCH Verlag Gmbh, Weinheim
T2  - Electroanalysis
T1  - Electrochemical Degradation of the Pesticide Dimethenamid-P at Gold, DSA Platinum and Ruthenium Oxide Electrodes in Different Electrolytes
EP  - 1880
IS  - 9
SP  - 1877
VL  - 26
DO  - 10.1002/elan.201400249
ER  - 
@article{
author = "Glavaski, Olivera and Petrović, Slobodan and Mijin, Dušan and Jovanović, Mica B. and Dugandžić, Ana M. and Zeremski, Tijana and Avramov-Ivić, Milka",
year = "2014",
abstract = "For the first time the electrochemical degradation of the pesticide dimethenamid-P was studied. Its direct electrochemical degradation, using potential cycling at a gold electrode, was performed by cyclic voltammetry and HPLC analysis of electrolyte after 72 h showed 56.8% of degradation. HPLC-MS indicates the formation of degradation products through the elimination of chlorine atom and C-N bond cleavage. By indirect electrolysis using DSA Ti/PtOx and DSA Ti/RuO2 electrodes during 30 minutes 87.2% and 88.3% of dimethenamid-P was degradated, respectively. The high percentage of degradation of dimethenamid-P was achieved with non time consuming, simple and cheap electrochemical processes.",
publisher = "Wiley-VCH Verlag Gmbh, Weinheim",
journal = "Electroanalysis",
title = "Electrochemical Degradation of the Pesticide Dimethenamid-P at Gold, DSA Platinum and Ruthenium Oxide Electrodes in Different Electrolytes",
pages = "1880-1877",
number = "9",
volume = "26",
doi = "10.1002/elan.201400249"
}
Glavaski, O., Petrović, S., Mijin, D., Jovanović, M. B., Dugandžić, A. M., Zeremski, T.,& Avramov-Ivić, M.. (2014). Electrochemical Degradation of the Pesticide Dimethenamid-P at Gold, DSA Platinum and Ruthenium Oxide Electrodes in Different Electrolytes. in Electroanalysis
Wiley-VCH Verlag Gmbh, Weinheim., 26(9), 1877-1880.
https://doi.org/10.1002/elan.201400249
Glavaski O, Petrović S, Mijin D, Jovanović MB, Dugandžić AM, Zeremski T, Avramov-Ivić M. Electrochemical Degradation of the Pesticide Dimethenamid-P at Gold, DSA Platinum and Ruthenium Oxide Electrodes in Different Electrolytes. in Electroanalysis. 2014;26(9):1877-1880.
doi:10.1002/elan.201400249 .
Glavaski, Olivera, Petrović, Slobodan, Mijin, Dušan, Jovanović, Mica B., Dugandžić, Ana M., Zeremski, Tijana, Avramov-Ivić, Milka, "Electrochemical Degradation of the Pesticide Dimethenamid-P at Gold, DSA Platinum and Ruthenium Oxide Electrodes in Different Electrolytes" in Electroanalysis, 26, no. 9 (2014):1877-1880,
https://doi.org/10.1002/elan.201400249 . .
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