Nešić, Jelena

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  • Nešić, Jelena (10)

Author's Bibliography

Supplementary material for the article: Aonyas, M. M.; Nešić, J.; Jović, M.; Marković, M.; Dojčinović, B.; Obradović, B.; Roglić, G. M. Degradation of Triton X-100 in Water Falling Film Dielectric Barrier Discharge Reactor. Clean - Soil, Air, Water 2016, 44 (4), 422–429. https://doi.org/10.1002/clen.201500501

Aonyas, Munera M.; Nešić, Jelena; Jović, Milica; Marković, Marijana; Dojčinović, Biljana P.; Obradović, Bratislav M.; Roglić, Goran

(Wiley-Blackwell, Hoboken, 2016)

TY  - DATA
AU  - Aonyas, Munera M.
AU  - Nešić, Jelena
AU  - Jović, Milica
AU  - Marković, Marijana
AU  - Dojčinović, Biljana P.
AU  - Obradović, Bratislav M.
AU  - Roglić, Goran
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3436
PB  - Wiley-Blackwell, Hoboken
T2  - CLEAN - Soil Air Water
T1  - Supplementary material for the article: Aonyas, M. M.; Nešić, J.; Jović, M.; Marković, M.; Dojčinović, B.; Obradović, B.; Roglić, G. M. Degradation of Triton X-100 in Water Falling Film Dielectric Barrier Discharge Reactor. Clean - Soil, Air, Water 2016, 44 (4), 422–429. https://doi.org/10.1002/clen.201500501
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3436
ER  - 
@misc{
author = "Aonyas, Munera M. and Nešić, Jelena and Jović, Milica and Marković, Marijana and Dojčinović, Biljana P. and Obradović, Bratislav M. and Roglić, Goran",
year = "2016",
publisher = "Wiley-Blackwell, Hoboken",
journal = "CLEAN - Soil Air Water",
title = "Supplementary material for the article: Aonyas, M. M.; Nešić, J.; Jović, M.; Marković, M.; Dojčinović, B.; Obradović, B.; Roglić, G. M. Degradation of Triton X-100 in Water Falling Film Dielectric Barrier Discharge Reactor. Clean - Soil, Air, Water 2016, 44 (4), 422–429. https://doi.org/10.1002/clen.201500501",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3436"
}
Aonyas, M. M., Nešić, J., Jović, M., Marković, M., Dojčinović, B. P., Obradović, B. M.,& Roglić, G.. (2016). Supplementary material for the article: Aonyas, M. M.; Nešić, J.; Jović, M.; Marković, M.; Dojčinović, B.; Obradović, B.; Roglić, G. M. Degradation of Triton X-100 in Water Falling Film Dielectric Barrier Discharge Reactor. Clean - Soil, Air, Water 2016, 44 (4), 422–429. https://doi.org/10.1002/clen.201500501. in CLEAN - Soil Air Water
Wiley-Blackwell, Hoboken..
https://hdl.handle.net/21.15107/rcub_cherry_3436
Aonyas MM, Nešić J, Jović M, Marković M, Dojčinović BP, Obradović BM, Roglić G. Supplementary material for the article: Aonyas, M. M.; Nešić, J.; Jović, M.; Marković, M.; Dojčinović, B.; Obradović, B.; Roglić, G. M. Degradation of Triton X-100 in Water Falling Film Dielectric Barrier Discharge Reactor. Clean - Soil, Air, Water 2016, 44 (4), 422–429. https://doi.org/10.1002/clen.201500501. in CLEAN - Soil Air Water. 2016;.
https://hdl.handle.net/21.15107/rcub_cherry_3436 .
Aonyas, Munera M., Nešić, Jelena, Jović, Milica, Marković, Marijana, Dojčinović, Biljana P., Obradović, Bratislav M., Roglić, Goran, "Supplementary material for the article: Aonyas, M. M.; Nešić, J.; Jović, M.; Marković, M.; Dojčinović, B.; Obradović, B.; Roglić, G. M. Degradation of Triton X-100 in Water Falling Film Dielectric Barrier Discharge Reactor. Clean - Soil, Air, Water 2016, 44 (4), 422–429. https://doi.org/10.1002/clen.201500501" in CLEAN - Soil Air Water (2016),
https://hdl.handle.net/21.15107/rcub_cherry_3436 .

Degradation of Triton X-100 in Water Falling Film Dielectric Barrier Discharge Reactor

Aonyas, Munera M.; Nešić, Jelena; Jović, Milica; Marković, Marijana; Dojčinović, Biljana P.; Obradović, Bratislav M.; Roglić, Goran

(Wiley-Blackwell, Hoboken, 2016)

TY  - JOUR
AU  - Aonyas, Munera M.
AU  - Nešić, Jelena
AU  - Jović, Milica
AU  - Marković, Marijana
AU  - Dojčinović, Biljana P.
AU  - Obradović, Bratislav M.
AU  - Roglić, Goran
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1920
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 Nešić, Jelena and Jović, Milica and Marković, Marijana and Dojčinović, Biljana P. 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., Nešić, J., Jović, M., Marković, M., Dojčinović, B. P., 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, Nešić J, Jović M, Marković M, Dojčinović BP, 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., Nešić, Jelena, Jović, Milica, Marković, Marijana, Dojčinović, Biljana P., 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 . .
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Degradation and detoxification of the 4-chlorophenol by non-thermal plasma-influence of homogeneous catalysts

Marković, Marijana; Dojčinović, Biljana P.; Obradović, Bratislav M.; Nešić, Jelena; Natić, Maja; Tosti, Tomislav; Kuraica, Milorad M.; Manojlović, Dragan D.

(Elsevier Science Bv, Amsterdam, 2015)

TY  - JOUR
AU  - Marković, Marijana
AU  - Dojčinović, Biljana P.
AU  - Obradović, Bratislav M.
AU  - Nešić, Jelena
AU  - Natić, Maja
AU  - Tosti, Tomislav
AU  - Kuraica, Milorad M.
AU  - Manojlović, Dragan D.
PY  - 2015
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1995
AB  - Experimental results of non-thermal plasma (NTP) utilization for degradation of 4-chlorphenol (4CP) with screening of toxicity were presented in this study. Degradation of 4CP was tested in the presence of homogeneous catalysts: hydrogen peroxide (H2O2) and iron (II) (Fe2+). The rate of degradation through eight consecutive passes of the 4CP solution in the NTP reactor was considered. Products of degradation as organic acids (acetic, formic or oxalic acid) and chloride were quantified using ion chromatography (IC). Anemia salina was used for the toxicity screening assay in order to estimate the potential and consequences of NTP reactor application in water treatment. The measured concentration of 4CP and degradation products confirmed very efficient removal of these substances from the water during the NTP treatment with the addition of a catalyst. Concerning bioassay, a significant difference in toxicity was determined between initial solution of 4CP in comparison with the solution exposed to catalytic NTP treatment. (C) 2015 Elsevier B.V. All rights reserved.
PB  - Elsevier Science Bv, Amsterdam
T2  - Separation and Purification Technology
T1  - Degradation and detoxification of the 4-chlorophenol by non-thermal plasma-influence of homogeneous catalysts
VL  - 154
SP  - 246
EP  - 254
DO  - 10.1016/j.seppur.2015.09.030
ER  - 
@article{
author = "Marković, Marijana and Dojčinović, Biljana P. and Obradović, Bratislav M. and Nešić, Jelena and Natić, Maja and Tosti, Tomislav and Kuraica, Milorad M. and Manojlović, Dragan D.",
year = "2015",
abstract = "Experimental results of non-thermal plasma (NTP) utilization for degradation of 4-chlorphenol (4CP) with screening of toxicity were presented in this study. Degradation of 4CP was tested in the presence of homogeneous catalysts: hydrogen peroxide (H2O2) and iron (II) (Fe2+). The rate of degradation through eight consecutive passes of the 4CP solution in the NTP reactor was considered. Products of degradation as organic acids (acetic, formic or oxalic acid) and chloride were quantified using ion chromatography (IC). Anemia salina was used for the toxicity screening assay in order to estimate the potential and consequences of NTP reactor application in water treatment. The measured concentration of 4CP and degradation products confirmed very efficient removal of these substances from the water during the NTP treatment with the addition of a catalyst. Concerning bioassay, a significant difference in toxicity was determined between initial solution of 4CP in comparison with the solution exposed to catalytic NTP treatment. (C) 2015 Elsevier B.V. All rights reserved.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Separation and Purification Technology",
title = "Degradation and detoxification of the 4-chlorophenol by non-thermal plasma-influence of homogeneous catalysts",
volume = "154",
pages = "246-254",
doi = "10.1016/j.seppur.2015.09.030"
}
Marković, M., Dojčinović, B. P., Obradović, B. M., Nešić, J., Natić, M., Tosti, T., Kuraica, M. M.,& Manojlović, D. D.. (2015). Degradation and detoxification of the 4-chlorophenol by non-thermal plasma-influence of homogeneous catalysts. in Separation and Purification Technology
Elsevier Science Bv, Amsterdam., 154, 246-254.
https://doi.org/10.1016/j.seppur.2015.09.030
Marković M, Dojčinović BP, Obradović BM, Nešić J, Natić M, Tosti T, Kuraica MM, Manojlović DD. Degradation and detoxification of the 4-chlorophenol by non-thermal plasma-influence of homogeneous catalysts. in Separation and Purification Technology. 2015;154:246-254.
doi:10.1016/j.seppur.2015.09.030 .
Marković, Marijana, Dojčinović, Biljana P., Obradović, Bratislav M., Nešić, Jelena, Natić, Maja, Tosti, Tomislav, Kuraica, Milorad M., Manojlović, Dragan D., "Degradation and detoxification of the 4-chlorophenol by non-thermal plasma-influence of homogeneous catalysts" in Separation and Purification Technology, 154 (2015):246-254,
https://doi.org/10.1016/j.seppur.2015.09.030 . .
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Fe Doped TiO2 Prepared by Microwave-Assisted Hydrothermal Process for Removal of As(III) and As(V) from Water

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

(Amer Chemical Soc, Washington, 2014)

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

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

(Serbian Chemical Soc, Belgrade, 2014)

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

Nešić, Jelena

(Универзитет у Београду, Хемијски факултет, 2014)

TY  - THES
AU  - Nešić, Jelena
PY  - 2014
UR  - http://eteze.bg.ac.rs/application/showtheses?thesesId=2279
UR  - https://fedorabg.bg.ac.rs/fedora/get/o:10143/bdef:Content/download
UR  - http://vbs.rs/scripts/cobiss?command=DISPLAY&base=70036&RID=45322767
UR  - http://nardus.mpn.gov.rs/123456789/4290
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2658
AB  - Sintetisani su modifikovani TiO2 fotokatalizatori hidrotermalnom metodompotpomognutom mikrotalasima za tretman otpadne vode iz tekstilne industrije. Fotokatalitičkaaktivnost katalizatora je procenjena na osnovu dekolorizacije reaktivne tekstilne boje ReactiveBlue 52 pomoću lampe sa Sunčevim spektrom zračenja.U prvom delu rada sintetisani su TiO2 katalizatori dopirani jonima La i kodopiranijonima La i V. Utvrđeno je da svi sintetisani katalizatori imaju mezoporoznu strukturu i dajoni oba dopanta utiču na morfološke i teksturalne osobine, povećavaju specifičnu površinu izapreminu pora, a smanjuju veličinu agregata. Dodatak V utiče na produženje apsorpcijekatalizatora u vidljivi deo spektra. Optimalna količina jona La kao dopanta je 2% i daljepovećanje sadržaja La vodi do smanjenja efikasnosti katalizatora, pa je katalizator sa 2% Laodabran za kodopovanje vanadijumom. Dodatak jona V u kodopiranim uzorcima dodatnodoprinosi povećanju fotokatalitičke aktivnosti i kao najefikasniji se pokazao katalizator sa 2%La i 0,02% V. Ispitivanjem uticaja početne koncentracije boje i katalizatora na dekolorizacijusa najefikasnijim katalizatorom, pokazalo se da procenat dekolorizacije opada sa povećanjempočetne koncentracije boje, a da se dekolorizacija povećava sa povećanjem koncentracijekatalizatora do jedne određene tačke, gde dostiže maksimum. Ovaj katalizator je pokazaoveću aktivnost i brzinu sedimentacije od komercijalno dostupnog Degussa P25 i mogućnostkorišćenja u više ciklusa bez gubitka aktivnosti, što čini ovaj katalizator prihvatljivim i zaindustrijsku primenu.U drugom delu rada je ispitana mogućnost primene TiO2 katalizatora dopiranogjonima Fe u heterogenom foto-Fentonskom procesu. Dopiranjem TiO2 jonima Femikrotalasno hidrotermalnom metodom dobijeni su materijali velike specifične površine irazvijene strukture mezopora i mikropora. Uočeno je da povećanje sadržaja jona Fe dovodi dopomeranja apsorcije katalizatora ka većim talasnim dužinama, u vidljivi region. Rezultatiispitivanja efikasnosti katalizatora za dekolorizaciju tekstilne boje su pokazali da katalizatordopiran Fe jonima ima veću aktivnost od nedopiranog TiO2. Prisustvo H2O2 povećavafotokatalitičku efikasnost kada se upotrebi u procesu sa TiO2, a u slučaju dopiranogkatalizatora sa 3,4% Fe, dodatak H2O2 povećava efikasnost u većoj meri nego za čist TiO2. Toznači da H2O2 zajedno sa dopiranim katalizatorom učestvuje u heterogenom foto-Fentonskomprocesu. Ispitivanjem uticaja količine dopanta na procenat dekolorizacije, došlo se dozaključka da je optimalna količina Fe 3,4% i pri višim koncentracijama dolazi do padaaktivnosti katalizatora. Rezultati ispitivanja uticaja pH su pokazali da se efikasnost povećavasa smanjenjem pH vrednosti i najbolji rezultati su dobijeni za pH vrednost 3, ali je curenje Fejona izraženo na ovako niskom pH, tako da je pH 4 odabran kao optimalna vrednost. Rezultatisu pokazali da koncentracija H2O2 ima uticaj na procenat dekolorizacije: procenatdekolorizacije se povećava sa povećanjem koncentracije H2O2 do 20 mM, nakon čega daljepovećanje nema značajan uticaj. Ispitivanje uticaja početne koncentracije boje i katalizatora jedalo iste rezultate kao i u slučaju katalizatora kodopiranog jonima La i V. Povećanjekoncentracije boje izaziva smanjenje procenta dekolorizacije, dok veća količina katalizatorapovećava efikasnost do jedne granične vrednosti, kada daljim povećanjem ne doprinosiefikasnosti procesa. Ispitivanjem degradacija 4-hlorfenola u heterogenom foto-Fentonskomprocesu sa najefikasnijim dopiranim TiO2 katalizatorom, 3,4% Fe, došlo se do zaključka da jekatalizator sposoban i za degradacije bezbojnih zagađivača. Ovaj katalizator je pokazao imogućnost ponovne upotrebe u više ciklusa bez gubitka aktivnosti. Uzimajući u obzir svenavedene osobine katalizatora, može se smatrati kao dobar kandidat za upotrebu uremedijaciji zagađenih voda.
AB  - Modified TiO2 photocatalysts were prepared by a microwave-assisted hydrothermalmethod for the treatment of textile industry wastewater. The photocatalytic activity of thesamples was evaluated by the decolorization of textile dye Reactive Blue 52 in aqueoussolutions under sun-like radiation.La doped and V-La co-doped TiO2 photocatalysts were synthesized. It was found thatall the synthesized catalysts had the mesoporous structure and ions of both dopants influencedmorphological and textural characteristics of the synthesized photocatalysts, increase specificsurface area and pore volume, as well as, reduce the size of aggregates. Vanadium dopingplays a role in extending light absorption into the visible region. The optimal amount oflanthanum doping is 2% and further increase of the lanthanum content leads to the decrease ofphotoactivity. Therefore, the catalyst with 2% of the lanthanum was chosen for co-dopingwith vanadium. The presence of V ions in the co-doped samples additionally contributes toenhancement of photoactivity and the photocatalyst with 2% La and 0.02% V appeared to bethe most photoactive. The effect of the initial dye concentration and catalyst loading with themost efficient catalyst were examined. It was found that percentage of dye removal decreaseswith the increase of initial dye concentration and the degradation increases with the increasingconcentration of the catalyst to a certain point, where it reaches its maximum. The V-La codopedcatalyst showed better photocatalytic activity and sedimentation properties thanDegussa P25 and also, excellent photostability and reusability, which make the V-La codopedcatalyst acceptable for industrial application.It was investigated the applicability of TiO2 catalyst doped with Fe ions inheterogeneous photo-Fenton process. It was found that all Fe doped materials prepared bymicrowave-assisted hydrothermal method have high specific surface area and mesoporousstructure. Fe doping influenced the extension of light absorption into the visible region. Theresults indicate that the addition of Fe contributes to the catalytic activity. The presence ofH2O2 increased the photocatalytic activity with TiO2, but with 3,4% Fe doped TiO2 increasedefficiency to a higher extent. It means that H2O2 has a part in the heterogeneous photo-Fentonprocess. It was found that the optimal amount of Fe doping is 3,4% and further increase of theFe content leads to the decrease of photoactivity. Results indicate that the efficiency increasewith decreasing the pH value and the best results are obtained for pH value 3, but leakage ofFe ions was observed at such low pH, therefore pH 4 was chosen as optimal. The resultsshowed that percentage of dye removal increases with the increase of H2O2 concentration to acertain point, where it reaches its maximum. The effect of the initial dye concentration andcatalyst loading gave the same results as in the case of V-La co-doped catalyst. Degradationof 4-chlorophenol in heterogeneous photo-Fenton process with 3,4% Fe doped catalyst wasexamined. Under the optimal experimental conditions, the catalyst was able to degrade evencolorless pollutant. The catalyst also showed the possibility of recycling without loss ofactivity. Therefore it can be considered as good candidate for wastewaters remediationpurpose.
PB  - Универзитет у Београду, Хемијски факултет
T2  - Универзитет у Београду
T1  - Sinteza i karakterizacija dopiranog mezoporoznog TiO2 sa unapređenim fotokatalitičkim osobinama za tretman otpadnih voda
T1  - Synthesis and characterisation of doped mesoporous TiO2 with advanced photocatalytic properties for waste water treatment
UR  - https://hdl.handle.net/21.15107/rcub_nardus_4290
ER  - 
@phdthesis{
author = "Nešić, Jelena",
year = "2014",
abstract = "Sintetisani su modifikovani TiO2 fotokatalizatori hidrotermalnom metodompotpomognutom mikrotalasima za tretman otpadne vode iz tekstilne industrije. Fotokatalitičkaaktivnost katalizatora je procenjena na osnovu dekolorizacije reaktivne tekstilne boje ReactiveBlue 52 pomoću lampe sa Sunčevim spektrom zračenja.U prvom delu rada sintetisani su TiO2 katalizatori dopirani jonima La i kodopiranijonima La i V. Utvrđeno je da svi sintetisani katalizatori imaju mezoporoznu strukturu i dajoni oba dopanta utiču na morfološke i teksturalne osobine, povećavaju specifičnu površinu izapreminu pora, a smanjuju veličinu agregata. Dodatak V utiče na produženje apsorpcijekatalizatora u vidljivi deo spektra. Optimalna količina jona La kao dopanta je 2% i daljepovećanje sadržaja La vodi do smanjenja efikasnosti katalizatora, pa je katalizator sa 2% Laodabran za kodopovanje vanadijumom. Dodatak jona V u kodopiranim uzorcima dodatnodoprinosi povećanju fotokatalitičke aktivnosti i kao najefikasniji se pokazao katalizator sa 2%La i 0,02% V. Ispitivanjem uticaja početne koncentracije boje i katalizatora na dekolorizacijusa najefikasnijim katalizatorom, pokazalo se da procenat dekolorizacije opada sa povećanjempočetne koncentracije boje, a da se dekolorizacija povećava sa povećanjem koncentracijekatalizatora do jedne određene tačke, gde dostiže maksimum. Ovaj katalizator je pokazaoveću aktivnost i brzinu sedimentacije od komercijalno dostupnog Degussa P25 i mogućnostkorišćenja u više ciklusa bez gubitka aktivnosti, što čini ovaj katalizator prihvatljivim i zaindustrijsku primenu.U drugom delu rada je ispitana mogućnost primene TiO2 katalizatora dopiranogjonima Fe u heterogenom foto-Fentonskom procesu. Dopiranjem TiO2 jonima Femikrotalasno hidrotermalnom metodom dobijeni su materijali velike specifične površine irazvijene strukture mezopora i mikropora. Uočeno je da povećanje sadržaja jona Fe dovodi dopomeranja apsorcije katalizatora ka većim talasnim dužinama, u vidljivi region. Rezultatiispitivanja efikasnosti katalizatora za dekolorizaciju tekstilne boje su pokazali da katalizatordopiran Fe jonima ima veću aktivnost od nedopiranog TiO2. Prisustvo H2O2 povećavafotokatalitičku efikasnost kada se upotrebi u procesu sa TiO2, a u slučaju dopiranogkatalizatora sa 3,4% Fe, dodatak H2O2 povećava efikasnost u većoj meri nego za čist TiO2. Toznači da H2O2 zajedno sa dopiranim katalizatorom učestvuje u heterogenom foto-Fentonskomprocesu. Ispitivanjem uticaja količine dopanta na procenat dekolorizacije, došlo se dozaključka da je optimalna količina Fe 3,4% i pri višim koncentracijama dolazi do padaaktivnosti katalizatora. Rezultati ispitivanja uticaja pH su pokazali da se efikasnost povećavasa smanjenjem pH vrednosti i najbolji rezultati su dobijeni za pH vrednost 3, ali je curenje Fejona izraženo na ovako niskom pH, tako da je pH 4 odabran kao optimalna vrednost. Rezultatisu pokazali da koncentracija H2O2 ima uticaj na procenat dekolorizacije: procenatdekolorizacije se povećava sa povećanjem koncentracije H2O2 do 20 mM, nakon čega daljepovećanje nema značajan uticaj. Ispitivanje uticaja početne koncentracije boje i katalizatora jedalo iste rezultate kao i u slučaju katalizatora kodopiranog jonima La i V. Povećanjekoncentracije boje izaziva smanjenje procenta dekolorizacije, dok veća količina katalizatorapovećava efikasnost do jedne granične vrednosti, kada daljim povećanjem ne doprinosiefikasnosti procesa. Ispitivanjem degradacija 4-hlorfenola u heterogenom foto-Fentonskomprocesu sa najefikasnijim dopiranim TiO2 katalizatorom, 3,4% Fe, došlo se do zaključka da jekatalizator sposoban i za degradacije bezbojnih zagađivača. Ovaj katalizator je pokazao imogućnost ponovne upotrebe u više ciklusa bez gubitka aktivnosti. Uzimajući u obzir svenavedene osobine katalizatora, može se smatrati kao dobar kandidat za upotrebu uremedijaciji zagađenih voda., Modified TiO2 photocatalysts were prepared by a microwave-assisted hydrothermalmethod for the treatment of textile industry wastewater. The photocatalytic activity of thesamples was evaluated by the decolorization of textile dye Reactive Blue 52 in aqueoussolutions under sun-like radiation.La doped and V-La co-doped TiO2 photocatalysts were synthesized. It was found thatall the synthesized catalysts had the mesoporous structure and ions of both dopants influencedmorphological and textural characteristics of the synthesized photocatalysts, increase specificsurface area and pore volume, as well as, reduce the size of aggregates. Vanadium dopingplays a role in extending light absorption into the visible region. The optimal amount oflanthanum doping is 2% and further increase of the lanthanum content leads to the decrease ofphotoactivity. Therefore, the catalyst with 2% of the lanthanum was chosen for co-dopingwith vanadium. The presence of V ions in the co-doped samples additionally contributes toenhancement of photoactivity and the photocatalyst with 2% La and 0.02% V appeared to bethe most photoactive. The effect of the initial dye concentration and catalyst loading with themost efficient catalyst were examined. It was found that percentage of dye removal decreaseswith the increase of initial dye concentration and the degradation increases with the increasingconcentration of the catalyst to a certain point, where it reaches its maximum. The V-La codopedcatalyst showed better photocatalytic activity and sedimentation properties thanDegussa P25 and also, excellent photostability and reusability, which make the V-La codopedcatalyst acceptable for industrial application.It was investigated the applicability of TiO2 catalyst doped with Fe ions inheterogeneous photo-Fenton process. It was found that all Fe doped materials prepared bymicrowave-assisted hydrothermal method have high specific surface area and mesoporousstructure. Fe doping influenced the extension of light absorption into the visible region. Theresults indicate that the addition of Fe contributes to the catalytic activity. The presence ofH2O2 increased the photocatalytic activity with TiO2, but with 3,4% Fe doped TiO2 increasedefficiency to a higher extent. It means that H2O2 has a part in the heterogeneous photo-Fentonprocess. It was found that the optimal amount of Fe doping is 3,4% and further increase of theFe content leads to the decrease of photoactivity. Results indicate that the efficiency increasewith decreasing the pH value and the best results are obtained for pH value 3, but leakage ofFe ions was observed at such low pH, therefore pH 4 was chosen as optimal. The resultsshowed that percentage of dye removal increases with the increase of H2O2 concentration to acertain point, where it reaches its maximum. The effect of the initial dye concentration andcatalyst loading gave the same results as in the case of V-La co-doped catalyst. Degradationof 4-chlorophenol in heterogeneous photo-Fenton process with 3,4% Fe doped catalyst wasexamined. Under the optimal experimental conditions, the catalyst was able to degrade evencolorless pollutant. The catalyst also showed the possibility of recycling without loss ofactivity. Therefore it can be considered as good candidate for wastewaters remediationpurpose.",
publisher = "Универзитет у Београду, Хемијски факултет",
journal = "Универзитет у Београду",
title = "Sinteza i karakterizacija dopiranog mezoporoznog TiO2 sa unapređenim fotokatalitičkim osobinama za tretman otpadnih voda, Synthesis and characterisation of doped mesoporous TiO2 with advanced photocatalytic properties for waste water treatment",
url = "https://hdl.handle.net/21.15107/rcub_nardus_4290"
}
Nešić, J.. (2014). Sinteza i karakterizacija dopiranog mezoporoznog TiO2 sa unapređenim fotokatalitičkim osobinama za tretman otpadnih voda. in Универзитет у Београду
Универзитет у Београду, Хемијски факултет..
https://hdl.handle.net/21.15107/rcub_nardus_4290
Nešić J. Sinteza i karakterizacija dopiranog mezoporoznog TiO2 sa unapređenim fotokatalitičkim osobinama za tretman otpadnih voda. in Универзитет у Београду. 2014;.
https://hdl.handle.net/21.15107/rcub_nardus_4290 .
Nešić, Jelena, "Sinteza i karakterizacija dopiranog mezoporoznog TiO2 sa unapređenim fotokatalitičkim osobinama za tretman otpadnih voda" in Универзитет у Београду (2014),
https://hdl.handle.net/21.15107/rcub_nardus_4290 .

New evidence for TiO2 uniform surfaces leading to complete bacterial reduction in the dark: Critical issues

Nešić, Jelena; Rtimi, Sami; Laub, Daniele; Roglić, Goran; Pulgarin, Cesar; Kiwi, John

(Elsevier Science Bv, Amsterdam, 2014)

TY  - JOUR
AU  - Nešić, Jelena
AU  - Rtimi, Sami
AU  - Laub, Daniele
AU  - Roglić, Goran
AU  - Pulgarin, Cesar
AU  - Kiwi, John
PY  - 2014
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1897
AB  - This study presents new evidence for the events leading to Escherichia coli reduction in the absence of light irradiation on TiO2-polyester (from now on TiO2-PES. By transmission electron microscopy (TEM) the diffusion of TiO2 NP's aggregates with the E. coli outer lipo-polyssacharide (LPS) layer is shown to be a prerequisite for the loss of bacterial cultivability. Within 30 min in the dark the TiO2 aggregates interact with E. coli cell wall leading within 120 min to the complete loss of bacterial cultivability on a TiO2-PES 5% TiO2 sample. The bacterial reduction was observed to increase with a higher TiO2 loading on the PES up to 5%. Bacterial disinfection on TiO2-PES in the dark was slower compared to the runs under low intensity simulated sunlight light irradiation. The interaction between the TiO2 aggregates and the E. coli cell wall is discussed in terms of the competition between the TiO2 units collapsing to form TiO2-aggregates at a physiologic pH-value followed by the electrostatic interaction with the bacteria surface. TiO2-PES samples were able to carry repetitive bacterial inactivation. This presents a potential for practical applications. X-ray photoelectron spectroscopy (XPS) evidence was found for the reduction of Ti4+ to Ti3+ contributing to redox interactions between TiO2-PES and the bacterial cell wall. Insight is provided into the mechanism of interaction between the E. coli cell wall and TiO2 NP's. The properties of the TiO2-PES surface like percentage atomic concentration, TiO2-loading, optical absorption, surface charge and crystallographic phases are reported in this study. (C) 2014 Elsevier B.V. All rights reserved.
PB  - Elsevier Science Bv, Amsterdam
T2  - Colloids and Surfaces. B: Biointerfaces
T1  - New evidence for TiO2 uniform surfaces leading to complete bacterial reduction in the dark: Critical issues
VL  - 123
SP  - 593
EP  - 599
DO  - 10.1016/j.colsurfb.2014.09.060
ER  - 
@article{
author = "Nešić, Jelena and Rtimi, Sami and Laub, Daniele and Roglić, Goran and Pulgarin, Cesar and Kiwi, John",
year = "2014",
abstract = "This study presents new evidence for the events leading to Escherichia coli reduction in the absence of light irradiation on TiO2-polyester (from now on TiO2-PES. By transmission electron microscopy (TEM) the diffusion of TiO2 NP's aggregates with the E. coli outer lipo-polyssacharide (LPS) layer is shown to be a prerequisite for the loss of bacterial cultivability. Within 30 min in the dark the TiO2 aggregates interact with E. coli cell wall leading within 120 min to the complete loss of bacterial cultivability on a TiO2-PES 5% TiO2 sample. The bacterial reduction was observed to increase with a higher TiO2 loading on the PES up to 5%. Bacterial disinfection on TiO2-PES in the dark was slower compared to the runs under low intensity simulated sunlight light irradiation. The interaction between the TiO2 aggregates and the E. coli cell wall is discussed in terms of the competition between the TiO2 units collapsing to form TiO2-aggregates at a physiologic pH-value followed by the electrostatic interaction with the bacteria surface. TiO2-PES samples were able to carry repetitive bacterial inactivation. This presents a potential for practical applications. X-ray photoelectron spectroscopy (XPS) evidence was found for the reduction of Ti4+ to Ti3+ contributing to redox interactions between TiO2-PES and the bacterial cell wall. Insight is provided into the mechanism of interaction between the E. coli cell wall and TiO2 NP's. The properties of the TiO2-PES surface like percentage atomic concentration, TiO2-loading, optical absorption, surface charge and crystallographic phases are reported in this study. (C) 2014 Elsevier B.V. All rights reserved.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Colloids and Surfaces. B: Biointerfaces",
title = "New evidence for TiO2 uniform surfaces leading to complete bacterial reduction in the dark: Critical issues",
volume = "123",
pages = "593-599",
doi = "10.1016/j.colsurfb.2014.09.060"
}
Nešić, J., Rtimi, S., Laub, D., Roglić, G., Pulgarin, C.,& Kiwi, J.. (2014). New evidence for TiO2 uniform surfaces leading to complete bacterial reduction in the dark: Critical issues. in Colloids and Surfaces. B: Biointerfaces
Elsevier Science Bv, Amsterdam., 123, 593-599.
https://doi.org/10.1016/j.colsurfb.2014.09.060
Nešić J, Rtimi S, Laub D, Roglić G, Pulgarin C, Kiwi J. New evidence for TiO2 uniform surfaces leading to complete bacterial reduction in the dark: Critical issues. in Colloids and Surfaces. B: Biointerfaces. 2014;123:593-599.
doi:10.1016/j.colsurfb.2014.09.060 .
Nešić, Jelena, Rtimi, Sami, Laub, Daniele, Roglić, Goran, Pulgarin, Cesar, Kiwi, John, "New evidence for TiO2 uniform surfaces leading to complete bacterial reduction in the dark: Critical issues" in Colloids and Surfaces. B: Biointerfaces, 123 (2014):593-599,
https://doi.org/10.1016/j.colsurfb.2014.09.060 . .
44
35
42
41

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

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

(Elsevier Science Bv, Amsterdam, 2013)

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

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

(Elsevier Science Bv, Amsterdam, 2013)

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

Dojčinović, Biljana P.; Roglić, Goran; Obradović, Bratislav M.; Kuraica, Milorad M.; Kostić, Mirjana M.; Nešić, Jelena; Manojlović, Dragan D.

(Elsevier Science Bv, Amsterdam, 2011)

TY  - JOUR
AU  - Dojčinović, Biljana P.
AU  - Roglić, Goran
AU  - Obradović, Bratislav M.
AU  - Kuraica, Milorad M.
AU  - Kostić, Mirjana M.
AU  - Nešić, Jelena
AU  - Manojlović, Dragan D.
PY  - 2011
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1184
AB  - Decolorization of reactive textile dyes Reactive Black 5, Reactive Blue 52, Reactive Yellow 125 and Reactive Green 15 was studied using advanced oxidation processes (AOPs) in a non-thermal plasma reactor, based on coaxial water falling film dielectric barrier discharge (DBD). Used initial dye concentrations in the solution were 40.0 and 80.0 mg/L. The effects of different initial pH of dye solutions, and addition of homogeneous catalysts (H(2)O(2), Fe(2+) and Cu(2+)) on the decolorization during subsequent recirculation of dye solution through the DBD reactor, i.e. applied energy density (45-315 kJ/L) were studied. Influence of residence time was investigated over a period of 24 h. Change of pH values and effect of pH adjustments of dye solution after each recirculation on the decolorization was also tested. It was found that the initial pH of dye solutions and pH adjustments of dye solution after each recirculation did not influence the decolorization. The most effective decolorization of 97% was obtained with addition of 10 mM H(2)O(2) in a system of 80.0 mg/L Reactive Black 5 with applied energy density of 45 kJ/L, after residence time of 24 h from plasma treatment. Toxicity was evaluated using the brine shrimp Artemia sauna as a test organism.
PB  - Elsevier Science Bv, Amsterdam
T2  - Journal of Hazardous Materials
T1  - Decolorization of reactive textile dyes using water falling film dielectric barrier discharge
VL  - 192
IS  - 2
SP  - 763
EP  - 771
DO  - 10.1016/j.jhazmat.2011.05.086
ER  - 
@article{
author = "Dojčinović, Biljana P. and Roglić, Goran and Obradović, Bratislav M. and Kuraica, Milorad M. and Kostić, Mirjana M. and Nešić, Jelena and Manojlović, Dragan D.",
year = "2011",
abstract = "Decolorization of reactive textile dyes Reactive Black 5, Reactive Blue 52, Reactive Yellow 125 and Reactive Green 15 was studied using advanced oxidation processes (AOPs) in a non-thermal plasma reactor, based on coaxial water falling film dielectric barrier discharge (DBD). Used initial dye concentrations in the solution were 40.0 and 80.0 mg/L. The effects of different initial pH of dye solutions, and addition of homogeneous catalysts (H(2)O(2), Fe(2+) and Cu(2+)) on the decolorization during subsequent recirculation of dye solution through the DBD reactor, i.e. applied energy density (45-315 kJ/L) were studied. Influence of residence time was investigated over a period of 24 h. Change of pH values and effect of pH adjustments of dye solution after each recirculation on the decolorization was also tested. It was found that the initial pH of dye solutions and pH adjustments of dye solution after each recirculation did not influence the decolorization. The most effective decolorization of 97% was obtained with addition of 10 mM H(2)O(2) in a system of 80.0 mg/L Reactive Black 5 with applied energy density of 45 kJ/L, after residence time of 24 h from plasma treatment. Toxicity was evaluated using the brine shrimp Artemia sauna as a test organism.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Journal of Hazardous Materials",
title = "Decolorization of reactive textile dyes using water falling film dielectric barrier discharge",
volume = "192",
number = "2",
pages = "763-771",
doi = "10.1016/j.jhazmat.2011.05.086"
}
Dojčinović, B. P., Roglić, G., Obradović, B. M., Kuraica, M. M., Kostić, M. M., Nešić, J.,& Manojlović, D. D.. (2011). Decolorization of reactive textile dyes using water falling film dielectric barrier discharge. in Journal of Hazardous Materials
Elsevier Science Bv, Amsterdam., 192(2), 763-771.
https://doi.org/10.1016/j.jhazmat.2011.05.086
Dojčinović BP, Roglić G, Obradović BM, Kuraica MM, Kostić MM, Nešić J, Manojlović DD. Decolorization of reactive textile dyes using water falling film dielectric barrier discharge. in Journal of Hazardous Materials. 2011;192(2):763-771.
doi:10.1016/j.jhazmat.2011.05.086 .
Dojčinović, Biljana P., Roglić, Goran, Obradović, Bratislav M., Kuraica, Milorad M., Kostić, Mirjana M., Nešić, Jelena, Manojlović, Dragan D., "Decolorization of reactive textile dyes using water falling film dielectric barrier discharge" in Journal of Hazardous Materials, 192, no. 2 (2011):763-771,
https://doi.org/10.1016/j.jhazmat.2011.05.086 . .
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