TY  - JOUR
AU  - Stevanović, Gordana
AU  - Jović-Jovičić, Nataša
AU  - Krstić, Jugoslav
AU  - Milutinović-Nikolić, Aleksandra D.
AU  - Banković, Predrag
AU  - Popović, Aleksandar R.
AU  - Ajduković, Marija
PY  - 2022
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/5662
AB  - Chitosan (Ch)-derived from biowaste along with smectite, an abundant clay mineral, were used in a low-cost and eco-friendly synthesis of a new type of catalyst. Nanocomposite catalysts constituted of Co supported on smectite with chitosan-derived carbon loading were obtained using an impregnation‑carbonization procedure and denoted as Co/cCh-S-T (T stands for applied carbonization temperature). The carbonization was performed in the temperature range from 400 °C to 700 °C in the flow of N2 providing inert atmosphere. The temperature of 500 °C was found to be the most suitable for catalyst synthesis regarding catalytic performance in a peroxymonosulfate activated degradation of tartrazine. The incorporation of carbonized chitosan structure within the interlamellar space of the smectite was confirmed using X-ray powder diffraction. The high-resolution transmission electron microscopy confirmed a layered structure of nanocomposites characteristic for smectite, as well as the presence of small spherical cobalt containing nanoformations (confirmed by energy dispersive X-ray spectroscopy) well dispersed within structure. The existance of cobalt in the CoII and CoIII oxidation state was proven by X-ray photoelectron spectroscopy. The Co/cCh-S-500 catalyst was proven to be stable and efficient after 5 consecutive cycles. This work showed that nanocomposite Co-catalysts, based on smectite and biowaste-derived carbon, as peroxymonosulfate activators exhibited a very promising performance in the degradation of water pollutants.
PB  - Elsevier
T2  - Applied Clay Science
T1  - Nanocomposite co-catalysts, based on smectite and biowaste-derived carbon, as peroxymonosulfate activators in degradation of tartrazine
VL  - 230
SP  - 106718
DO  - 10.1016/j.clay.2022.106718
ER  - 

@article{
author = "Stevanović, Gordana and Jović-Jovičić, Nataša and Krstić, Jugoslav and Milutinović-Nikolić, Aleksandra D. and Banković, Predrag and Popović, Aleksandar R. and Ajduković, Marija",
year = "2022",
abstract = "Chitosan (Ch)-derived from biowaste along with smectite, an abundant clay mineral, were used in a low-cost and eco-friendly synthesis of a new type of catalyst. Nanocomposite catalysts constituted of Co supported on smectite with chitosan-derived carbon loading were obtained using an impregnation‑carbonization procedure and denoted as Co/cCh-S-T (T stands for applied carbonization temperature). The carbonization was performed in the temperature range from 400 °C to 700 °C in the flow of N2 providing inert atmosphere. The temperature of 500 °C was found to be the most suitable for catalyst synthesis regarding catalytic performance in a peroxymonosulfate activated degradation of tartrazine. The incorporation of carbonized chitosan structure within the interlamellar space of the smectite was confirmed using X-ray powder diffraction. The high-resolution transmission electron microscopy confirmed a layered structure of nanocomposites characteristic for smectite, as well as the presence of small spherical cobalt containing nanoformations (confirmed by energy dispersive X-ray spectroscopy) well dispersed within structure. The existance of cobalt in the CoII and CoIII oxidation state was proven by X-ray photoelectron spectroscopy. The Co/cCh-S-500 catalyst was proven to be stable and efficient after 5 consecutive cycles. This work showed that nanocomposite Co-catalysts, based on smectite and biowaste-derived carbon, as peroxymonosulfate activators exhibited a very promising performance in the degradation of water pollutants.",
publisher = "Elsevier",
journal = "Applied Clay Science",
title = "Nanocomposite co-catalysts, based on smectite and biowaste-derived carbon, as peroxymonosulfate activators in degradation of tartrazine",
volume = "230",
pages = "106718",
doi = "10.1016/j.clay.2022.106718"
}

Stevanović, G., Jović-Jovičić, N., Krstić, J., Milutinović-Nikolić, A. D., Banković, P., Popović, A. R.,& Ajduković, M.. (2022). Nanocomposite co-catalysts, based on smectite and biowaste-derived carbon, as peroxymonosulfate activators in degradation of tartrazine. in Applied Clay Science
Elsevier., 230, 106718.
https://doi.org/10.1016/j.clay.2022.106718

Stevanović G, Jović-Jovičić N, Krstić J, Milutinović-Nikolić AD, Banković P, Popović AR, Ajduković M. Nanocomposite co-catalysts, based on smectite and biowaste-derived carbon, as peroxymonosulfate activators in degradation of tartrazine. in Applied Clay Science. 2022;230:106718.
doi:10.1016/j.clay.2022.106718 .

Stevanović, Gordana, Jović-Jovičić, Nataša, Krstić, Jugoslav, Milutinović-Nikolić, Aleksandra D., Banković, Predrag, Popović, Aleksandar R., Ajduković, Marija, "Nanocomposite co-catalysts, based on smectite and biowaste-derived carbon, as peroxymonosulfate activators in degradation of tartrazine" in Applied Clay Science, 230 (2022):106718,
https://doi.org/10.1016/j.clay.2022.106718 . .

TY  - DATA
AU  - Stevanović, Gordana
AU  - Jović-Jovičić, Nataša
AU  - Krstić, Jugoslav
AU  - Milutinović-Nikolić, Aleksandra D.
AU  - Banković, Predrag
AU  - Popović, Aleksandar R.
AU  - Ajduković, Marija
PY  - 2022
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/5671
AB  - Chitosan (Ch)-derived from biowaste along with smectite, an abundant clay mineral, were used in a low-cost and eco-friendly synthesis of a new type of catalyst. Nanocomposite catalysts constituted of Co supported on smectite with chitosan-derived carbon loading were obtained using an impregnation‑carbonization procedure and denoted as Co/cCh-S-T (T stands for applied carbonization temperature). The carbonization was performed in the temperature range from 400 °C to 700 °C in the flow of N2 providing inert atmosphere. The temperature of 500 °C was found to be the most suitable for catalyst synthesis regarding catalytic performance in a peroxymonosulfate activated degradation of tartrazine. The incorporation of carbonized chitosan structure within the interlamellar space of the smectite was confirmed using X-ray powder diffraction. The high-resolution transmission electron microscopy confirmed a layered structure of nanocomposites characteristic for smectite, as well as the presence of small spherical cobalt containing nanoformations (confirmed by energy dispersive X-ray spectroscopy) well dispersed within structure. The existance of cobalt in the CoII and CoIII oxidation state was proven by X-ray photoelectron spectroscopy. The Co/cCh-S-500 catalyst was proven to be stable and efficient after 5 consecutive cycles. This work showed that nanocomposite Co-catalysts, based on smectite and biowaste-derived carbon, as peroxymonosulfate activators exhibited a very promising performance in the degradation of water pollutants.
PB  - Elsevier
T2  - Applied Clay Science
T1  - Supplementary material for: Stevanović, G., Jović-Jovičić, N., Krstić, J., Milutinović-Nikolić, A., Banković, P., Popović, A.,& Ajduković, M.. (2022). Nanocomposite co-catalysts, based on smectite and biowaste-derived carbon, as peroxymonosulfate activators in degradation of tartrazine. in Applied Clay Science Elsevier., 230, 106718. https://doi.org/10.1016/j.clay.2022.106718
VL  - 230
SP  - 106718
UR  - https://hdl.handle.net/21.15107/rcub_cherry_5671
ER  - 

@misc{
author = "Stevanović, Gordana and Jović-Jovičić, Nataša and Krstić, Jugoslav and Milutinović-Nikolić, Aleksandra D. and Banković, Predrag and Popović, Aleksandar R. and Ajduković, Marija",
year = "2022",
abstract = "Chitosan (Ch)-derived from biowaste along with smectite, an abundant clay mineral, were used in a low-cost and eco-friendly synthesis of a new type of catalyst. Nanocomposite catalysts constituted of Co supported on smectite with chitosan-derived carbon loading were obtained using an impregnation‑carbonization procedure and denoted as Co/cCh-S-T (T stands for applied carbonization temperature). The carbonization was performed in the temperature range from 400 °C to 700 °C in the flow of N2 providing inert atmosphere. The temperature of 500 °C was found to be the most suitable for catalyst synthesis regarding catalytic performance in a peroxymonosulfate activated degradation of tartrazine. The incorporation of carbonized chitosan structure within the interlamellar space of the smectite was confirmed using X-ray powder diffraction. The high-resolution transmission electron microscopy confirmed a layered structure of nanocomposites characteristic for smectite, as well as the presence of small spherical cobalt containing nanoformations (confirmed by energy dispersive X-ray spectroscopy) well dispersed within structure. The existance of cobalt in the CoII and CoIII oxidation state was proven by X-ray photoelectron spectroscopy. The Co/cCh-S-500 catalyst was proven to be stable and efficient after 5 consecutive cycles. This work showed that nanocomposite Co-catalysts, based on smectite and biowaste-derived carbon, as peroxymonosulfate activators exhibited a very promising performance in the degradation of water pollutants.",
publisher = "Elsevier",
journal = "Applied Clay Science",
title = "Supplementary material for: Stevanović, G., Jović-Jovičić, N., Krstić, J., Milutinović-Nikolić, A., Banković, P., Popović, A.,& Ajduković, M.. (2022). Nanocomposite co-catalysts, based on smectite and biowaste-derived carbon, as peroxymonosulfate activators in degradation of tartrazine. in Applied Clay Science Elsevier., 230, 106718. https://doi.org/10.1016/j.clay.2022.106718",
volume = "230",
pages = "106718",
url = "https://hdl.handle.net/21.15107/rcub_cherry_5671"
}

Stevanović, G., Jović-Jovičić, N., Krstić, J., Milutinović-Nikolić, A. D., Banković, P., Popović, A. R.,& Ajduković, M.. (2022). Supplementary material for: Stevanović, G., Jović-Jovičić, N., Krstić, J., Milutinović-Nikolić, A., Banković, P., Popović, A.,& Ajduković, M.. (2022). Nanocomposite co-catalysts, based on smectite and biowaste-derived carbon, as peroxymonosulfate activators in degradation of tartrazine. in Applied Clay Science Elsevier., 230, 106718. https://doi.org/10.1016/j.clay.2022.106718. in Applied Clay Science
Elsevier., 230, 106718.
https://hdl.handle.net/21.15107/rcub_cherry_5671

Stevanović G, Jović-Jovičić N, Krstić J, Milutinović-Nikolić AD, Banković P, Popović AR, Ajduković M. Supplementary material for: Stevanović, G., Jović-Jovičić, N., Krstić, J., Milutinović-Nikolić, A., Banković, P., Popović, A.,& Ajduković, M.. (2022). Nanocomposite co-catalysts, based on smectite and biowaste-derived carbon, as peroxymonosulfate activators in degradation of tartrazine. in Applied Clay Science Elsevier., 230, 106718. https://doi.org/10.1016/j.clay.2022.106718. in Applied Clay Science. 2022;230:106718.
https://hdl.handle.net/21.15107/rcub_cherry_5671 .

Stevanović, Gordana, Jović-Jovičić, Nataša, Krstić, Jugoslav, Milutinović-Nikolić, Aleksandra D., Banković, Predrag, Popović, Aleksandar R., Ajduković, Marija, "Supplementary material for: Stevanović, G., Jović-Jovičić, N., Krstić, J., Milutinović-Nikolić, A., Banković, P., Popović, A.,& Ajduković, M.. (2022). Nanocomposite co-catalysts, based on smectite and biowaste-derived carbon, as peroxymonosulfate activators in degradation of tartrazine. in Applied Clay Science Elsevier., 230, 106718. https://doi.org/10.1016/j.clay.2022.106718" in Applied Clay Science, 230 (2022):106718,
https://hdl.handle.net/21.15107/rcub_cherry_5671 .

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

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

Ilić, I., Milutinović-Nikolić, A. D., Mojović, Z. D., Vuković, Z., Vulić, P. J., Gržetić, I., Banković, P.,& Jović-Jovičić, N.. (2020). Oxidative degradation of aromatic N-compounds using cobalt containing montmorillonite-based catalysts. in Applied Clay Science
Elsevier., 193, 105668.
https://doi.org/10.1016/j.clay.2020.105668

Ilić I, Milutinović-Nikolić AD, Mojović ZD, Vuković Z, Vulić PJ, Gržetić I, Banković P, Jović-Jovičić N. Oxidative degradation of aromatic N-compounds using cobalt containing montmorillonite-based catalysts. in Applied Clay Science. 2020;193:105668.
doi:10.1016/j.clay.2020.105668 .

Ilić, Ilija, Milutinović-Nikolić, Aleksandra D., Mojović, Zorica D., Vuković, Zoran, Vulić, Predrag J., Gržetić, Ivan, Banković, Predrag, Jović-Jovičić, Nataša, "Oxidative degradation of aromatic N-compounds using cobalt containing montmorillonite-based catalysts" in Applied Clay Science, 193 (2020):105668,
https://doi.org/10.1016/j.clay.2020.105668 . .

TY  - DATA
AU  - Ilić, Ilija
AU  - Milutinović-Nikolić, Aleksandra D.
AU  - Mojović, Zorica D.
AU  - Vuković, Zoran
AU  - Vulić, Predrag J.
AU  - Gržetić, Ivan
AU  - Banković, Predrag
AU  - Jović-Jovičić, Nataša
PY  - 2020
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/4046
PB  - Elsevier
T2  - Applied Clay Science
T1  - Supplementary data for the article: Ilić, I.; Milutinović-Nikolić, A.; Mojović, Z.; Vuković, Z.; Vulić, P.; Gržetić, I.; Banković, P.; Jović-Jovičić, N. Oxidative Degradation of Aromatic N-Compounds Using Cobalt Containing Montmorillonite-Based Catalysts. Applied Clay Science 2020, 193, 105668. https://doi.org/10.1016/j.clay.2020.105668
UR  - https://hdl.handle.net/21.15107/rcub_cherry_4046
ER  - 

@misc{
author = "Ilić, Ilija and Milutinović-Nikolić, Aleksandra D. and Mojović, Zorica D. and Vuković, Zoran and Vulić, Predrag J. and Gržetić, Ivan and Banković, Predrag and Jović-Jovičić, Nataša",
year = "2020",
publisher = "Elsevier",
journal = "Applied Clay Science",
title = "Supplementary data for the article: Ilić, I.; Milutinović-Nikolić, A.; Mojović, Z.; Vuković, Z.; Vulić, P.; Gržetić, I.; Banković, P.; Jović-Jovičić, N. Oxidative Degradation of Aromatic N-Compounds Using Cobalt Containing Montmorillonite-Based Catalysts. Applied Clay Science 2020, 193, 105668. https://doi.org/10.1016/j.clay.2020.105668",
url = "https://hdl.handle.net/21.15107/rcub_cherry_4046"
}

Ilić, I., Milutinović-Nikolić, A. D., Mojović, Z. D., Vuković, Z., Vulić, P. J., Gržetić, I., Banković, P.,& Jović-Jovičić, N.. (2020). Supplementary data for the article: Ilić, I.; Milutinović-Nikolić, A.; Mojović, Z.; Vuković, Z.; Vulić, P.; Gržetić, I.; Banković, P.; Jović-Jovičić, N. Oxidative Degradation of Aromatic N-Compounds Using Cobalt Containing Montmorillonite-Based Catalysts. Applied Clay Science 2020, 193, 105668. https://doi.org/10.1016/j.clay.2020.105668. in Applied Clay Science
Elsevier..
https://hdl.handle.net/21.15107/rcub_cherry_4046

Ilić I, Milutinović-Nikolić AD, Mojović ZD, Vuković Z, Vulić PJ, Gržetić I, Banković P, Jović-Jovičić N. Supplementary data for the article: Ilić, I.; Milutinović-Nikolić, A.; Mojović, Z.; Vuković, Z.; Vulić, P.; Gržetić, I.; Banković, P.; Jović-Jovičić, N. Oxidative Degradation of Aromatic N-Compounds Using Cobalt Containing Montmorillonite-Based Catalysts. Applied Clay Science 2020, 193, 105668. https://doi.org/10.1016/j.clay.2020.105668. in Applied Clay Science. 2020;.
https://hdl.handle.net/21.15107/rcub_cherry_4046 .

Ilić, Ilija, Milutinović-Nikolić, Aleksandra D., Mojović, Zorica D., Vuković, Zoran, Vulić, Predrag J., Gržetić, Ivan, Banković, Predrag, Jović-Jovičić, Nataša, "Supplementary data for the article: Ilić, I.; Milutinović-Nikolić, A.; Mojović, Z.; Vuković, Z.; Vulić, P.; Gržetić, I.; Banković, P.; Jović-Jovičić, N. Oxidative Degradation of Aromatic N-Compounds Using Cobalt Containing Montmorillonite-Based Catalysts. Applied Clay Science 2020, 193, 105668. https://doi.org/10.1016/j.clay.2020.105668" in Applied Clay Science (2020),
https://hdl.handle.net/21.15107/rcub_cherry_4046 .

TY  - DATA
AU  - Marković, Marija
AU  - Marinović, Sanja
AU  - Mudrinić, Tihana
AU  - Ajduković, Marija
AU  - Jović-Jovičić, Nataša
AU  - Mojović, Zorica D.
AU  - Orlić, Jovana
AU  - Milutinović-Nikolić, Aleksandra D.
AU  - Banković, Predrag
PY  - 2019
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3375
T2  - Applied Clay Science
T1  - Supplementary material for the article: Marković, M.; Marinović, S.; Mudrinić, T.; Ajduković, M.; Jović-Jovičić, N.; Mojović, Z.; Orlić, J.; Milutinović-Nikolić, A.; Banković, P. Co(II) Impregnated Al(III)-Pillared Montmorillonite–Synthesis, Characterization and Catalytic Properties in Oxone® Activation for Dye Degradation. Applied Clay Science 2019, 182. https://doi.org/10.1016/j.clay.2019.105276
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3375
ER  - 

@misc{
author = "Marković, Marija and Marinović, Sanja and Mudrinić, Tihana and Ajduković, Marija and Jović-Jovičić, Nataša and Mojović, Zorica D. and Orlić, Jovana and Milutinović-Nikolić, Aleksandra D. and Banković, Predrag",
year = "2019",
journal = "Applied Clay Science",
title = "Supplementary material for the article: Marković, M.; Marinović, S.; Mudrinić, T.; Ajduković, M.; Jović-Jovičić, N.; Mojović, Z.; Orlić, J.; Milutinović-Nikolić, A.; Banković, P. Co(II) Impregnated Al(III)-Pillared Montmorillonite–Synthesis, Characterization and Catalytic Properties in Oxone® Activation for Dye Degradation. Applied Clay Science 2019, 182. https://doi.org/10.1016/j.clay.2019.105276",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3375"
}

Marković, M., Marinović, S., Mudrinić, T., Ajduković, M., Jović-Jovičić, N., Mojović, Z. D., Orlić, J., Milutinović-Nikolić, A. D.,& Banković, P.. (2019). Supplementary material for the article: Marković, M.; Marinović, S.; Mudrinić, T.; Ajduković, M.; Jović-Jovičić, N.; Mojović, Z.; Orlić, J.; Milutinović-Nikolić, A.; Banković, P. Co(II) Impregnated Al(III)-Pillared Montmorillonite–Synthesis, Characterization and Catalytic Properties in Oxone® Activation for Dye Degradation. Applied Clay Science 2019, 182. https://doi.org/10.1016/j.clay.2019.105276. in Applied Clay Science.
https://hdl.handle.net/21.15107/rcub_cherry_3375

Marković M, Marinović S, Mudrinić T, Ajduković M, Jović-Jovičić N, Mojović ZD, Orlić J, Milutinović-Nikolić AD, Banković P. Supplementary material for the article: Marković, M.; Marinović, S.; Mudrinić, T.; Ajduković, M.; Jović-Jovičić, N.; Mojović, Z.; Orlić, J.; Milutinović-Nikolić, A.; Banković, P. Co(II) Impregnated Al(III)-Pillared Montmorillonite–Synthesis, Characterization and Catalytic Properties in Oxone® Activation for Dye Degradation. Applied Clay Science 2019, 182. https://doi.org/10.1016/j.clay.2019.105276. in Applied Clay Science. 2019;.
https://hdl.handle.net/21.15107/rcub_cherry_3375 .

Marković, Marija, Marinović, Sanja, Mudrinić, Tihana, Ajduković, Marija, Jović-Jovičić, Nataša, Mojović, Zorica D., Orlić, Jovana, Milutinović-Nikolić, Aleksandra D., Banković, Predrag, "Supplementary material for the article: Marković, M.; Marinović, S.; Mudrinić, T.; Ajduković, M.; Jović-Jovičić, N.; Mojović, Z.; Orlić, J.; Milutinović-Nikolić, A.; Banković, P. Co(II) Impregnated Al(III)-Pillared Montmorillonite–Synthesis, Characterization and Catalytic Properties in Oxone® Activation for Dye Degradation. Applied Clay Science 2019, 182. https://doi.org/10.1016/j.clay.2019.105276" in Applied Clay Science (2019),
https://hdl.handle.net/21.15107/rcub_cherry_3375 .

TY  - JOUR
AU  - Marković, Marija
AU  - Marinović, Sanja
AU  - Mudrinić, Tihana
AU  - Ajduković, Marija
AU  - Jović-Jovičić, Nataša
AU  - Mojović, Zorica D.
AU  - Orlić, Jovana
AU  - Milutinović-Nikolić, Aleksandra D.
AU  - Banković, Predrag
PY  - 2019
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3374
AB  - Aluminum pillared clay was synthesized and impregnated with Co2+ (CoAP), using incipient wetness impregnation method. The obtained CoAP was characterized by chemical analysis, XRPD, SEM with EDS, XPS and low temperature N2 physisorption. By these methods the incorporation of Co2+ was confirmed in both micro and mesoporous region. The synthesized material was investigated as a catalyst in catalytic oxidation of organic water pollutants – dyes – in the presence of Oxone® (peroxymonosulfate). Oxone® is a precursor of sulfate radicals. Tartrazine was chosen as a model dye pollutant. The influence of the mass of the catalyst, temperature and initial pH was investigated. Temperature increase was beneficial for dye degradation rate. The reaction rate was the highest for initial pH values around those corresponding to neutral conditions, somewhat slower for pH < 4 values, while for pH > 10 decolorization was significantly less expressed. Along with decolorization of tartrazine solution the formation and degradation of tartrazine catalytic oxidation products were monitored using UV–Vis spectroscopy. CoAP was found to be efficient catalyst in Oxone® induced catalytic degradation of both tartrazine and detected products of its degradation.
T2  - Applied Clay Science
T1  - Co(II) impregnated Al(III)-pillared montmorillonite–Synthesis, characterization and catalytic properties in Oxone® activation for dye degradation
VL  - 182
DO  - 10.1016/j.clay.2019.105276
ER  - 

@article{
author = "Marković, Marija and Marinović, Sanja and Mudrinić, Tihana and Ajduković, Marija and Jović-Jovičić, Nataša and Mojović, Zorica D. and Orlić, Jovana and Milutinović-Nikolić, Aleksandra D. and Banković, Predrag",
year = "2019",
abstract = "Aluminum pillared clay was synthesized and impregnated with Co2+ (CoAP), using incipient wetness impregnation method. The obtained CoAP was characterized by chemical analysis, XRPD, SEM with EDS, XPS and low temperature N2 physisorption. By these methods the incorporation of Co2+ was confirmed in both micro and mesoporous region. The synthesized material was investigated as a catalyst in catalytic oxidation of organic water pollutants – dyes – in the presence of Oxone® (peroxymonosulfate). Oxone® is a precursor of sulfate radicals. Tartrazine was chosen as a model dye pollutant. The influence of the mass of the catalyst, temperature and initial pH was investigated. Temperature increase was beneficial for dye degradation rate. The reaction rate was the highest for initial pH values around those corresponding to neutral conditions, somewhat slower for pH < 4 values, while for pH > 10 decolorization was significantly less expressed. Along with decolorization of tartrazine solution the formation and degradation of tartrazine catalytic oxidation products were monitored using UV–Vis spectroscopy. CoAP was found to be efficient catalyst in Oxone® induced catalytic degradation of both tartrazine and detected products of its degradation.",
journal = "Applied Clay Science",
title = "Co(II) impregnated Al(III)-pillared montmorillonite–Synthesis, characterization and catalytic properties in Oxone® activation for dye degradation",
volume = "182",
doi = "10.1016/j.clay.2019.105276"
}

Marković, M., Marinović, S., Mudrinić, T., Ajduković, M., Jović-Jovičić, N., Mojović, Z. D., Orlić, J., Milutinović-Nikolić, A. D.,& Banković, P.. (2019). Co(II) impregnated Al(III)-pillared montmorillonite–Synthesis, characterization and catalytic properties in Oxone® activation for dye degradation. in Applied Clay Science, 182.
https://doi.org/10.1016/j.clay.2019.105276

Marković M, Marinović S, Mudrinić T, Ajduković M, Jović-Jovičić N, Mojović ZD, Orlić J, Milutinović-Nikolić AD, Banković P. Co(II) impregnated Al(III)-pillared montmorillonite–Synthesis, characterization and catalytic properties in Oxone® activation for dye degradation. in Applied Clay Science. 2019;182.
doi:10.1016/j.clay.2019.105276 .

Marković, Marija, Marinović, Sanja, Mudrinić, Tihana, Ajduković, Marija, Jović-Jovičić, Nataša, Mojović, Zorica D., Orlić, Jovana, Milutinović-Nikolić, Aleksandra D., Banković, Predrag, "Co(II) impregnated Al(III)-pillared montmorillonite–Synthesis, characterization and catalytic properties in Oxone® activation for dye degradation" in Applied Clay Science, 182 (2019),
https://doi.org/10.1016/j.clay.2019.105276 . .

TY  - DATA
AU  - Anđelković, Uroš
AU  - Milutinović-Nikolić, Aleksandra D.
AU  - Jović-Jovičić, Nataša
AU  - Banković, Predrag
AU  - Bajt, Teja
AU  - Mojović, Zorica D.
AU  - Vujčić, Zoran
AU  - Jovanović, Dušan
PY  - 2015
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3365
AB  - The external invertase isoform 1 (EINV1) was immobilised on eight differently modified beidellite nanoclays, Modifications were composed of organo-modification with different amounts of surfactant - hexadecyl trimethylammonium cation (HDTMA), pillaring with Al/Fe containing polyhydroxy cations and acid modification of Na-enriched and pillared clays. The modified nanoclays were characterised by XRD, N-2-physisorption, SEM and FT-IR spectroscopy. The amount of bound enzyme activity was significantly influenced by the modification of beidellite ranging from 50 to remarkable 2200 U/g. Biochemical characterization was performed for five modified nanoclays showing the highest enzyme activity after invertase immobilisation. The investigation demonstrated that after immobilisation the structure and the catalytic properties of invertase were preserved, while Km values were slightly increased from 26 to 37 mM. immobilisation significantly improved thermal and storage stability of EINV1. Results indicate that beidellite nanoclays obtained by low cost modifications can be applied as a suitable support for the immobilisation of invertase. The immobilizate can be efficiently engaged in sucrose hydrolysis in batch reactor.
PB  - Elsevier Sci Ltd, Oxford
T2  - Food Chemistry
T1  - Supplementary data for article: Andjelković, U.; Milutinović-Nikolić, A.; Jović-Jovičić, N.; Banković, P.; Bajt, T.; Mojović, Z.; Vujčić, Z.; Jovanović, D. Efficient Stabilization of Saccharomyces Cerevisiae External Invertase by Immobilisation on Modified Beidellite Nanoclays. Food Chemistry 2015, 168, 262–269. https://doi.org/10.1016/j.foodchem.2014.07.055
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3365
ER  - 

@misc{
author = "Anđelković, Uroš and Milutinović-Nikolić, Aleksandra D. and Jović-Jovičić, Nataša and Banković, Predrag and Bajt, Teja and Mojović, Zorica D. and Vujčić, Zoran and Jovanović, Dušan",
year = "2015",
abstract = "The external invertase isoform 1 (EINV1) was immobilised on eight differently modified beidellite nanoclays, Modifications were composed of organo-modification with different amounts of surfactant - hexadecyl trimethylammonium cation (HDTMA), pillaring with Al/Fe containing polyhydroxy cations and acid modification of Na-enriched and pillared clays. The modified nanoclays were characterised by XRD, N-2-physisorption, SEM and FT-IR spectroscopy. The amount of bound enzyme activity was significantly influenced by the modification of beidellite ranging from 50 to remarkable 2200 U/g. Biochemical characterization was performed for five modified nanoclays showing the highest enzyme activity after invertase immobilisation. The investigation demonstrated that after immobilisation the structure and the catalytic properties of invertase were preserved, while Km values were slightly increased from 26 to 37 mM. immobilisation significantly improved thermal and storage stability of EINV1. Results indicate that beidellite nanoclays obtained by low cost modifications can be applied as a suitable support for the immobilisation of invertase. The immobilizate can be efficiently engaged in sucrose hydrolysis in batch reactor.",
publisher = "Elsevier Sci Ltd, Oxford",
journal = "Food Chemistry",
title = "Supplementary data for article: Andjelković, U.; Milutinović-Nikolić, A.; Jović-Jovičić, N.; Banković, P.; Bajt, T.; Mojović, Z.; Vujčić, Z.; Jovanović, D. Efficient Stabilization of Saccharomyces Cerevisiae External Invertase by Immobilisation on Modified Beidellite Nanoclays. Food Chemistry 2015, 168, 262–269. https://doi.org/10.1016/j.foodchem.2014.07.055",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3365"
}

Anđelković, U., Milutinović-Nikolić, A. D., Jović-Jovičić, N., Banković, P., Bajt, T., Mojović, Z. D., Vujčić, Z.,& Jovanović, D.. (2015). Supplementary data for article: Andjelković, U.; Milutinović-Nikolić, A.; Jović-Jovičić, N.; Banković, P.; Bajt, T.; Mojović, Z.; Vujčić, Z.; Jovanović, D. Efficient Stabilization of Saccharomyces Cerevisiae External Invertase by Immobilisation on Modified Beidellite Nanoclays. Food Chemistry 2015, 168, 262–269. https://doi.org/10.1016/j.foodchem.2014.07.055. in Food Chemistry
Elsevier Sci Ltd, Oxford..
https://hdl.handle.net/21.15107/rcub_cherry_3365

Anđelković U, Milutinović-Nikolić AD, Jović-Jovičić N, Banković P, Bajt T, Mojović ZD, Vujčić Z, Jovanović D. Supplementary data for article: Andjelković, U.; Milutinović-Nikolić, A.; Jović-Jovičić, N.; Banković, P.; Bajt, T.; Mojović, Z.; Vujčić, Z.; Jovanović, D. Efficient Stabilization of Saccharomyces Cerevisiae External Invertase by Immobilisation on Modified Beidellite Nanoclays. Food Chemistry 2015, 168, 262–269. https://doi.org/10.1016/j.foodchem.2014.07.055. in Food Chemistry. 2015;.
https://hdl.handle.net/21.15107/rcub_cherry_3365 .

Anđelković, Uroš, Milutinović-Nikolić, Aleksandra D., Jović-Jovičić, Nataša, Banković, Predrag, Bajt, Teja, Mojović, Zorica D., Vujčić, Zoran, Jovanović, Dušan, "Supplementary data for article: Andjelković, U.; Milutinović-Nikolić, A.; Jović-Jovičić, N.; Banković, P.; Bajt, T.; Mojović, Z.; Vujčić, Z.; Jovanović, D. Efficient Stabilization of Saccharomyces Cerevisiae External Invertase by Immobilisation on Modified Beidellite Nanoclays. Food Chemistry 2015, 168, 262–269. https://doi.org/10.1016/j.foodchem.2014.07.055" in Food Chemistry (2015),
https://hdl.handle.net/21.15107/rcub_cherry_3365 .

TY  - JOUR
AU  - Anđelković, Uroš
AU  - Milutinović-Nikolić, Aleksandra D.
AU  - Jović-Jovičić, Nataša
AU  - Banković, Predrag
AU  - Bajt, Teja
AU  - Mojović, Zorica D.
AU  - Vujčić, Zoran
AU  - Jovanović, Dušan
PY  - 2015
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1865
AB  - The external invertase isoform 1 (EINV1) was immobilised on eight differently modified beidellite nanoclays, Modifications were composed of organo-modification with different amounts of surfactant - hexadecyl trimethylammonium cation (HDTMA), pillaring with Al/Fe containing polyhydroxy cations and acid modification of Na-enriched and pillared clays. The modified nanoclays were characterised by XRD, N-2-physisorption, SEM and FT-IR spectroscopy. The amount of bound enzyme activity was significantly influenced by the modification of beidellite ranging from 50 to remarkable 2200 U/g. Biochemical characterization was performed for five modified nanoclays showing the highest enzyme activity after invertase immobilisation. The investigation demonstrated that after immobilisation the structure and the catalytic properties of invertase were preserved, while Km values were slightly increased from 26 to 37 mM. immobilisation significantly improved thermal and storage stability of EINV1. Results indicate that beidellite nanoclays obtained by low cost modifications can be applied as a suitable support for the immobilisation of invertase. The immobilizate can be efficiently engaged in sucrose hydrolysis in batch reactor.
PB  - Elsevier Sci Ltd, Oxford
T2  - Food Chemistry
T1  - Efficient stabilization of Saccharomyces cerevisiae external invertase by immobilisation on modified beidellite nanoclays
VL  - 168
SP  - 262
EP  - 269
DO  - 10.1016/j.foodchem.2014.07.055
ER  - 

@article{
author = "Anđelković, Uroš and Milutinović-Nikolić, Aleksandra D. and Jović-Jovičić, Nataša and Banković, Predrag and Bajt, Teja and Mojović, Zorica D. and Vujčić, Zoran and Jovanović, Dušan",
year = "2015",
abstract = "The external invertase isoform 1 (EINV1) was immobilised on eight differently modified beidellite nanoclays, Modifications were composed of organo-modification with different amounts of surfactant - hexadecyl trimethylammonium cation (HDTMA), pillaring with Al/Fe containing polyhydroxy cations and acid modification of Na-enriched and pillared clays. The modified nanoclays were characterised by XRD, N-2-physisorption, SEM and FT-IR spectroscopy. The amount of bound enzyme activity was significantly influenced by the modification of beidellite ranging from 50 to remarkable 2200 U/g. Biochemical characterization was performed for five modified nanoclays showing the highest enzyme activity after invertase immobilisation. The investigation demonstrated that after immobilisation the structure and the catalytic properties of invertase were preserved, while Km values were slightly increased from 26 to 37 mM. immobilisation significantly improved thermal and storage stability of EINV1. Results indicate that beidellite nanoclays obtained by low cost modifications can be applied as a suitable support for the immobilisation of invertase. The immobilizate can be efficiently engaged in sucrose hydrolysis in batch reactor.",
publisher = "Elsevier Sci Ltd, Oxford",
journal = "Food Chemistry",
title = "Efficient stabilization of Saccharomyces cerevisiae external invertase by immobilisation on modified beidellite nanoclays",
volume = "168",
pages = "262-269",
doi = "10.1016/j.foodchem.2014.07.055"
}

Anđelković, U., Milutinović-Nikolić, A. D., Jović-Jovičić, N., Banković, P., Bajt, T., Mojović, Z. D., Vujčić, Z.,& Jovanović, D.. (2015). Efficient stabilization of Saccharomyces cerevisiae external invertase by immobilisation on modified beidellite nanoclays. in Food Chemistry
Elsevier Sci Ltd, Oxford., 168, 262-269.
https://doi.org/10.1016/j.foodchem.2014.07.055

Anđelković U, Milutinović-Nikolić AD, Jović-Jovičić N, Banković P, Bajt T, Mojović ZD, Vujčić Z, Jovanović D. Efficient stabilization of Saccharomyces cerevisiae external invertase by immobilisation on modified beidellite nanoclays. in Food Chemistry. 2015;168:262-269.
doi:10.1016/j.foodchem.2014.07.055 .

Anđelković, Uroš, Milutinović-Nikolić, Aleksandra D., Jović-Jovičić, Nataša, Banković, Predrag, Bajt, Teja, Mojović, Zorica D., Vujčić, Zoran, Jovanović, Dušan, "Efficient stabilization of Saccharomyces cerevisiae external invertase by immobilisation on modified beidellite nanoclays" in Food Chemistry, 168 (2015):262-269,
https://doi.org/10.1016/j.foodchem.2014.07.055 . .

TY  - JOUR
AU  - Milutinović-Nikolić, Aleksandra D.
AU  - Maksin, D.
AU  - Jovic-Jovicic, N.
AU  - Mirković, Marija D.
AU  - Stanković, Dalibor
AU  - Mojović, Zorica D.
AU  - Bankovic, P.
PY  - 2014
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1809
AB  - (99)Technetium is one of the largest components of nuclear waste material. In aqueous solutions Tc-99 is present as the pertechnetate oxoanion, (TcO4-)-Tc-99, which is highly soluble and mobile in groundwater under oxidizing conditions, thus posing a major environmental concern. In this study, a series of organo-modified bentonite clay samples was tested as adsorbents for the removal of radioactive (TcO4-)-Tc-99 from aqueous solution at room temperature. The influence of the hexadecyl trimethylammonium (HDTMA)/bentonite ratio on the adsorption ability of the organobentonites was investigated. It was found that the adsorbent in which the exchangeable cations were only partially substituted with HDTMA showed very low affinity toward pertechnetate. On the other hand, the adsorbents in which the HDTMA loading exceeded the cation exchange capacity (CEC) value had high efficiency. The behavior of such adsorbents was best described by a Freundlich isotherm, while for the sample in which the HDTMA loading was equal to the CEC, the linear adsorption isotherm was the most appropriate. The difference in adsorption performance of several adsorbents was discussed from the point of view of the interlayer arrangement of the HDTMA. The kinetics of pertechnetate adsorption on HDTMA-bentonites was tested and analyzed using different surface reaction- and diffusion-based kinetic models. For all the investigated adsorbents, the most appropriate kinetic model was the pseudo-second-order kinetics model. The obtained adsorption capacities were and HDTMA-bentonites with HDTMA loadings exceeding CEC value should be regarded as very promising adsorbents for the remediation of Tc-99 polluted waters. (C) 2014 Elsevier B.V. All rights reserved.
PB  - Elsevier Science Bv, Amsterdam
T2  - Applied Clay Science
T1  - Removal of Tc-99(VII) by organo-modified bentonite
VL  - 95
SP  - 294
EP  - 302
DO  - 10.1016/j.clay.2014.04.027
ER  - 

@article{
author = "Milutinović-Nikolić, Aleksandra D. and Maksin, D. and Jovic-Jovicic, N. and Mirković, Marija D. and Stanković, Dalibor and Mojović, Zorica D. and Bankovic, P.",
year = "2014",
abstract = "(99)Technetium is one of the largest components of nuclear waste material. In aqueous solutions Tc-99 is present as the pertechnetate oxoanion, (TcO4-)-Tc-99, which is highly soluble and mobile in groundwater under oxidizing conditions, thus posing a major environmental concern. In this study, a series of organo-modified bentonite clay samples was tested as adsorbents for the removal of radioactive (TcO4-)-Tc-99 from aqueous solution at room temperature. The influence of the hexadecyl trimethylammonium (HDTMA)/bentonite ratio on the adsorption ability of the organobentonites was investigated. It was found that the adsorbent in which the exchangeable cations were only partially substituted with HDTMA showed very low affinity toward pertechnetate. On the other hand, the adsorbents in which the HDTMA loading exceeded the cation exchange capacity (CEC) value had high efficiency. The behavior of such adsorbents was best described by a Freundlich isotherm, while for the sample in which the HDTMA loading was equal to the CEC, the linear adsorption isotherm was the most appropriate. The difference in adsorption performance of several adsorbents was discussed from the point of view of the interlayer arrangement of the HDTMA. The kinetics of pertechnetate adsorption on HDTMA-bentonites was tested and analyzed using different surface reaction- and diffusion-based kinetic models. For all the investigated adsorbents, the most appropriate kinetic model was the pseudo-second-order kinetics model. The obtained adsorption capacities were and HDTMA-bentonites with HDTMA loadings exceeding CEC value should be regarded as very promising adsorbents for the remediation of Tc-99 polluted waters. (C) 2014 Elsevier B.V. All rights reserved.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Applied Clay Science",
title = "Removal of Tc-99(VII) by organo-modified bentonite",
volume = "95",
pages = "294-302",
doi = "10.1016/j.clay.2014.04.027"
}

Milutinović-Nikolić, A. D., Maksin, D., Jovic-Jovicic, N., Mirković, M. D., Stanković, D., Mojović, Z. D.,& Bankovic, P.. (2014). Removal of Tc-99(VII) by organo-modified bentonite. in Applied Clay Science
Elsevier Science Bv, Amsterdam., 95, 294-302.
https://doi.org/10.1016/j.clay.2014.04.027

Milutinović-Nikolić AD, Maksin D, Jovic-Jovicic N, Mirković MD, Stanković D, Mojović ZD, Bankovic P. Removal of Tc-99(VII) by organo-modified bentonite. in Applied Clay Science. 2014;95:294-302.
doi:10.1016/j.clay.2014.04.027 .

Milutinović-Nikolić, Aleksandra D., Maksin, D., Jovic-Jovicic, N., Mirković, Marija D., Stanković, Dalibor, Mojović, Zorica D., Bankovic, P., "Removal of Tc-99(VII) by organo-modified bentonite" in Applied Clay Science, 95 (2014):294-302,
https://doi.org/10.1016/j.clay.2014.04.027 . .

TY  - JOUR
AU  - Zunic, Marija J.
AU  - Milutinović-Nikolić, Aleksandra D.
AU  - Stanković, Dalibor
AU  - Manojlović, Dragan D.
AU  - Jović-Jovičić, Nataša
AU  - Banković, Predrag
AU  - Mojović, Zorica D.
AU  - Jovanović, Dušan M.
PY  - 2014
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1833
AB  - Bentonite clay rich in smectite clay mineral from seldom investigated locality Mecji Do (MD) in Serbia was modified. The organomodification was performed with different loadings of benzyltrimethylammonium (BTMA) cation. The characterization of clay-based samples was performed, including XRD, FTIR and chemical and textural analysis. Electrochemical investigation was performed on a glassy carbon electrode (GCE) support with thin film of homogenously deposited either Na-enriched or one of organomodified clays forming composite electrodes. The behavior of the composite electrodes in the electrooxidation of p-nitrophenol (p-NP) in acidic media was analyzed using multisweep cyclic voltammetry. Oxidation of p-NP occurred at 1.2 V vs. Ag/AgCl for all investigated electrodes. The results indicate that the incorporation of BTMA cations into smectite enhanced the electrode stability toward the electrooxidation of p-NP in comparison to bare GCE and composite electrode based on Na-enriched clay. The current density for the p-NP oxidation wave slightly decreased with the increase of BTMA loading. On the other hand the electrode stability was significantly improved with the increase of BTMA loading. (C) 2014 Elsevier B.V. All rights reserved.
PB  - Elsevier Science Bv, Amsterdam
T2  - Applied Surface Science
T1  - Electrooxidation of p-nitrophenol using a composite organo-smectite clay glassy carbon electrode
VL  - 313
SP  - 440
EP  - 448
DO  - 10.1016/j.apsusc.2014.05.228
ER  - 

@article{
author = "Zunic, Marija J. and Milutinović-Nikolić, Aleksandra D. and Stanković, Dalibor and Manojlović, Dragan D. and Jović-Jovičić, Nataša and Banković, Predrag and Mojović, Zorica D. and Jovanović, Dušan M.",
year = "2014",
abstract = "Bentonite clay rich in smectite clay mineral from seldom investigated locality Mecji Do (MD) in Serbia was modified. The organomodification was performed with different loadings of benzyltrimethylammonium (BTMA) cation. The characterization of clay-based samples was performed, including XRD, FTIR and chemical and textural analysis. Electrochemical investigation was performed on a glassy carbon electrode (GCE) support with thin film of homogenously deposited either Na-enriched or one of organomodified clays forming composite electrodes. The behavior of the composite electrodes in the electrooxidation of p-nitrophenol (p-NP) in acidic media was analyzed using multisweep cyclic voltammetry. Oxidation of p-NP occurred at 1.2 V vs. Ag/AgCl for all investigated electrodes. The results indicate that the incorporation of BTMA cations into smectite enhanced the electrode stability toward the electrooxidation of p-NP in comparison to bare GCE and composite electrode based on Na-enriched clay. The current density for the p-NP oxidation wave slightly decreased with the increase of BTMA loading. On the other hand the electrode stability was significantly improved with the increase of BTMA loading. (C) 2014 Elsevier B.V. All rights reserved.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Applied Surface Science",
title = "Electrooxidation of p-nitrophenol using a composite organo-smectite clay glassy carbon electrode",
volume = "313",
pages = "440-448",
doi = "10.1016/j.apsusc.2014.05.228"
}

Zunic, M. J., Milutinović-Nikolić, A. D., Stanković, D., Manojlović, D. D., Jović-Jovičić, N., Banković, P., Mojović, Z. D.,& Jovanović, D. M.. (2014). Electrooxidation of p-nitrophenol using a composite organo-smectite clay glassy carbon electrode. in Applied Surface Science
Elsevier Science Bv, Amsterdam., 313, 440-448.
https://doi.org/10.1016/j.apsusc.2014.05.228

Zunic MJ, Milutinović-Nikolić AD, Stanković D, Manojlović DD, Jović-Jovičić N, Banković P, Mojović ZD, Jovanović DM. Electrooxidation of p-nitrophenol using a composite organo-smectite clay glassy carbon electrode. in Applied Surface Science. 2014;313:440-448.
doi:10.1016/j.apsusc.2014.05.228 .

Zunic, Marija J., Milutinović-Nikolić, Aleksandra D., Stanković, Dalibor, Manojlović, Dragan D., Jović-Jovičić, Nataša, Banković, Predrag, Mojović, Zorica D., Jovanović, Dušan M., "Electrooxidation of p-nitrophenol using a composite organo-smectite clay glassy carbon electrode" in Applied Surface Science, 313 (2014):440-448,
https://doi.org/10.1016/j.apsusc.2014.05.228 . .

TY  - JOUR
AU  - Sandic, Zvjezdana P.
AU  - Zunic, Marija J.
AU  - Maksin, Danijela D.
AU  - Milutinović-Nikolić, Aleksandra D.
AU  - Popović, Aleksandar R.
AU  - Jovanovic, Dugan M.
AU  - Nastasović, Aleksandra B.
PY  - 2014
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1643
AB  - In this paper, macroporous glycidyl methacrylate and ethylene glycol dimethacrylate copolymer functionalized with diethylene triamine (PGME-deta), was evaluated as Reactive Black 5 (RB5) sorbent. Batch RB5 removal from aqueous solution by PGME-deta was investigated by varying pH, contact time, sorbent dosage, initial dye concentration and temperature. The sorption is pH sensitive having maximum at pH 2 (dye removal of 85%), decreasing with the increase of pH (dye removal of 24% at pH 11) after 60 min. Sorption kinetics was fitted to chemical-reaction and particle-diffusion models (pseudo-first-, pseudo-second-order, intraparticle diffusion and Mckay models). The pseudo-second-order kinetic model accurately predicted the RB5 amount sorbed under all investigated operating conditions, while the intraparticle diffusion was the dominant rate-limiting mechanism. The diffusion mechanism was more prevalent with the decrease in temperature and the increase in concentration. The isotherm data was best fitted with the Langmuir model, indicating homogeneous distribution of active sites on PGME-deta and monolayer sorption, with the maximum sorption capacity of 353 mg g(-1). The calculated sorption rates improved with increasing temperature and an activation energy close to 40 kj mol(-1) was determined, suggesting that chemisorption was also rate-controlling.
AB  - U okviru ovog rada ispitana je mogućnost korišćenja makroporoznog kopolimera glicidilmetakrilata i etilenglikoldimetakrilata funkcionalizovanog reakcijom otvaranja epoksidnih grupa sa dietilentriaminom (PGME-deta) kao sorbenta reaktivne tekstilne boje Reactive Black 5 (RB5). U šaržnim uslovima je ispitano uklanjanje RB5 iz vodenog rastvora pomoću PGME-deta, variranjem pH, vremena kontakta, mase sorbenta, početne koncentracije boje i temperature. PGME-deta je pokazao afinitet za sorpciju RB5 zbog prisustva protonovanih amino grupa koje privlače anjonske sulfonatne grupe u molekulu boje i mogućnosti stvaranja vodoničnih veza između sorbenta i sorbata. Kinetika sorpcije je analizirana pomoću četiri kinetička modela (pseudo-prvog, pseudo-drugog reda, unutarčestične difuzije i Mekej) da bi se odredilo koji model najbolje opisuje sorpciju RB5. Zapažen je izrazit uticaj pH vrednosti na sorpciju RB5, sa maksimumom na pH 2 (pri čemu je efikasnost uklanjanja boje 85%), i smanjenjem količine sorbovane boje sa povećanjem pH (količina uklonjene boje na pH 11 posle 60 min iznosi samo 24%). Izučavanjem kinetike sorpcije pokazalo se da sorpcija RB5 pomoću PGME-deta sledi kinetički model pseudo-drugog reda (PSO), sugerišući da je brzina sorpcije kontrolisana kapacitetom sorbenta i koncentracijom sorbata. Mehanizam procesa dominantno čini unutarčestična difuzija, uz manji uticaj difuzije kroz film. Ovi mehanizmi difuzije su izraženiji pri nižim temperaturama i većim koncentracijama. Langmirov model najbolje opisuje ravnotežnu izotermu, ukazujući na homogenu raspodelu aktivnih mesta na površini PGME-deta i monoslojnu sorpciju. Maksimalni sorpcioni kapacitet izračunat iz Langmirove izoterme iznosi 353 mg g-1. Zapaženo je da se brzina sorpcije povećava sa povećanjem temperature. Izračunata vrednost aktivacione energije od oko 40 kJ mol-1 potvrđuje da se radi o procesu koji dominantno kontroliše hemisorpcija.
PB  - Assoc Chemical Engineers Serbia, Belgrade
T2  - Hemijska industrija
T1  - Glycidyl methacrylate macroporous copolymer grafted with diethylene triamine as sorbent for Reactive Black 5
T1  - Makroporozni kopolimer na bazi glicidilmetakrilata funkcionalizovan sa dietilentriaminom kao sorbent tekstilne boje Reactive Black 5
VL  - 68
IS  - 6
SP  - 685
EP  - 699
DO  - 10.2298/HEMIND140127023S
ER  - 

@article{
author = "Sandic, Zvjezdana P. and Zunic, Marija J. and Maksin, Danijela D. and Milutinović-Nikolić, Aleksandra D. and Popović, Aleksandar R. and Jovanovic, Dugan M. and Nastasović, Aleksandra B.",
year = "2014",
abstract = "In this paper, macroporous glycidyl methacrylate and ethylene glycol dimethacrylate copolymer functionalized with diethylene triamine (PGME-deta), was evaluated as Reactive Black 5 (RB5) sorbent. Batch RB5 removal from aqueous solution by PGME-deta was investigated by varying pH, contact time, sorbent dosage, initial dye concentration and temperature. The sorption is pH sensitive having maximum at pH 2 (dye removal of 85%), decreasing with the increase of pH (dye removal of 24% at pH 11) after 60 min. Sorption kinetics was fitted to chemical-reaction and particle-diffusion models (pseudo-first-, pseudo-second-order, intraparticle diffusion and Mckay models). The pseudo-second-order kinetic model accurately predicted the RB5 amount sorbed under all investigated operating conditions, while the intraparticle diffusion was the dominant rate-limiting mechanism. The diffusion mechanism was more prevalent with the decrease in temperature and the increase in concentration. The isotherm data was best fitted with the Langmuir model, indicating homogeneous distribution of active sites on PGME-deta and monolayer sorption, with the maximum sorption capacity of 353 mg g(-1). The calculated sorption rates improved with increasing temperature and an activation energy close to 40 kj mol(-1) was determined, suggesting that chemisorption was also rate-controlling., U okviru ovog rada ispitana je mogućnost korišćenja makroporoznog kopolimera glicidilmetakrilata i etilenglikoldimetakrilata funkcionalizovanog reakcijom otvaranja epoksidnih grupa sa dietilentriaminom (PGME-deta) kao sorbenta reaktivne tekstilne boje Reactive Black 5 (RB5). U šaržnim uslovima je ispitano uklanjanje RB5 iz vodenog rastvora pomoću PGME-deta, variranjem pH, vremena kontakta, mase sorbenta, početne koncentracije boje i temperature. PGME-deta je pokazao afinitet za sorpciju RB5 zbog prisustva protonovanih amino grupa koje privlače anjonske sulfonatne grupe u molekulu boje i mogućnosti stvaranja vodoničnih veza između sorbenta i sorbata. Kinetika sorpcije je analizirana pomoću četiri kinetička modela (pseudo-prvog, pseudo-drugog reda, unutarčestične difuzije i Mekej) da bi se odredilo koji model najbolje opisuje sorpciju RB5. Zapažen je izrazit uticaj pH vrednosti na sorpciju RB5, sa maksimumom na pH 2 (pri čemu je efikasnost uklanjanja boje 85%), i smanjenjem količine sorbovane boje sa povećanjem pH (količina uklonjene boje na pH 11 posle 60 min iznosi samo 24%). Izučavanjem kinetike sorpcije pokazalo se da sorpcija RB5 pomoću PGME-deta sledi kinetički model pseudo-drugog reda (PSO), sugerišući da je brzina sorpcije kontrolisana kapacitetom sorbenta i koncentracijom sorbata. Mehanizam procesa dominantno čini unutarčestična difuzija, uz manji uticaj difuzije kroz film. Ovi mehanizmi difuzije su izraženiji pri nižim temperaturama i većim koncentracijama. Langmirov model najbolje opisuje ravnotežnu izotermu, ukazujući na homogenu raspodelu aktivnih mesta na površini PGME-deta i monoslojnu sorpciju. Maksimalni sorpcioni kapacitet izračunat iz Langmirove izoterme iznosi 353 mg g-1. Zapaženo je da se brzina sorpcije povećava sa povećanjem temperature. Izračunata vrednost aktivacione energije od oko 40 kJ mol-1 potvrđuje da se radi o procesu koji dominantno kontroliše hemisorpcija.",
publisher = "Assoc Chemical Engineers Serbia, Belgrade",
journal = "Hemijska industrija",
title = "Glycidyl methacrylate macroporous copolymer grafted with diethylene triamine as sorbent for Reactive Black 5, Makroporozni kopolimer na bazi glicidilmetakrilata funkcionalizovan sa dietilentriaminom kao sorbent tekstilne boje Reactive Black 5",
volume = "68",
number = "6",
pages = "685-699",
doi = "10.2298/HEMIND140127023S"
}

Sandic, Z. P., Zunic, M. J., Maksin, D. D., Milutinović-Nikolić, A. D., Popović, A. R., Jovanovic, D. M.,& Nastasović, A. B.. (2014). Glycidyl methacrylate macroporous copolymer grafted with diethylene triamine as sorbent for Reactive Black 5. in Hemijska industrija
Assoc Chemical Engineers Serbia, Belgrade., 68(6), 685-699.
https://doi.org/10.2298/HEMIND140127023S

Sandic ZP, Zunic MJ, Maksin DD, Milutinović-Nikolić AD, Popović AR, Jovanovic DM, Nastasović AB. Glycidyl methacrylate macroporous copolymer grafted with diethylene triamine as sorbent for Reactive Black 5. in Hemijska industrija. 2014;68(6):685-699.
doi:10.2298/HEMIND140127023S .

Sandic, Zvjezdana P., Zunic, Marija J., Maksin, Danijela D., Milutinović-Nikolić, Aleksandra D., Popović, Aleksandar R., Jovanovic, Dugan M., Nastasović, Aleksandra B., "Glycidyl methacrylate macroporous copolymer grafted with diethylene triamine as sorbent for Reactive Black 5" in Hemijska industrija, 68, no. 6 (2014):685-699,
https://doi.org/10.2298/HEMIND140127023S . .

TY  - JOUR
AU  - Jovic-Jovicic, N. P.
AU  - Milutinović-Nikolić, Aleksandra D.
AU  - Zunic, M. J.
AU  - Mojović, Zorica D.
AU  - Bankovic, P. T.
AU  - Gržetić, Ivan
AU  - Jovanović, Dušan M.
PY  - 2013
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1362
AB  - Two series of organobentonites (OBs) were synthesized from Na+-exchanged bentonite clay from Bogovina, Serbia. In the first series the starting material was modified using hexadecyltrimethylammonium (HDTMA(+)) ion in the amounts corresponding to 0.2, 0.5, 1.0 and 2.0 of the CEC value. The second series was obtained using quaternary alkyl ammonium cations (QAACs) with different alkyl chain lengths: hexadecyltrimethylammonium (HDTMA(+)), dodecyltrimethylammonium (DDTMA(+)) and tetramethylammonium (TMA(+)) ions. The synthesized OBs were characterized. The adsorption of anionic reactive dye Reactive Black 5 (RB5) and Pb2+ from single component solutions and their hi-component solution was investigated for both series of OBs. The adsorptive properties of the OBs were correlated to the amount and type of incorporated QAACs. The correlation was tested using different mathematical models and best fits were found. Experimental results showed that simultaneous adsorption of RB5 and Pb2+ exhibited synergic effect. The adsorption capacity for both RB5 and Pb2+ was higher in their hi-component solution than in single-component solutions. These results indicate the creation of new adsorption sites during the simultaneous adsorption.
PB  - Elsevier Science Bv, Amsterdam
T2  - Journal of Contaminant Hydrology
T1  - Synergic adsorption of Pb2+ and reactive dye-RB5 on two series of organomodified bentonites
VL  - 150
SP  - 1
EP  - 11
DO  - 10.1016/j.jconhyd.2013.03.004
ER  - 

@article{
author = "Jovic-Jovicic, N. P. and Milutinović-Nikolić, Aleksandra D. and Zunic, M. J. and Mojović, Zorica D. and Bankovic, P. T. and Gržetić, Ivan and Jovanović, Dušan M.",
year = "2013",
abstract = "Two series of organobentonites (OBs) were synthesized from Na+-exchanged bentonite clay from Bogovina, Serbia. In the first series the starting material was modified using hexadecyltrimethylammonium (HDTMA(+)) ion in the amounts corresponding to 0.2, 0.5, 1.0 and 2.0 of the CEC value. The second series was obtained using quaternary alkyl ammonium cations (QAACs) with different alkyl chain lengths: hexadecyltrimethylammonium (HDTMA(+)), dodecyltrimethylammonium (DDTMA(+)) and tetramethylammonium (TMA(+)) ions. The synthesized OBs were characterized. The adsorption of anionic reactive dye Reactive Black 5 (RB5) and Pb2+ from single component solutions and their hi-component solution was investigated for both series of OBs. The adsorptive properties of the OBs were correlated to the amount and type of incorporated QAACs. The correlation was tested using different mathematical models and best fits were found. Experimental results showed that simultaneous adsorption of RB5 and Pb2+ exhibited synergic effect. The adsorption capacity for both RB5 and Pb2+ was higher in their hi-component solution than in single-component solutions. These results indicate the creation of new adsorption sites during the simultaneous adsorption.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Journal of Contaminant Hydrology",
title = "Synergic adsorption of Pb2+ and reactive dye-RB5 on two series of organomodified bentonites",
volume = "150",
pages = "1-11",
doi = "10.1016/j.jconhyd.2013.03.004"
}

Jovic-Jovicic, N. P., Milutinović-Nikolić, A. D., Zunic, M. J., Mojović, Z. D., Bankovic, P. T., Gržetić, I.,& Jovanović, D. M.. (2013). Synergic adsorption of Pb2+ and reactive dye-RB5 on two series of organomodified bentonites. in Journal of Contaminant Hydrology
Elsevier Science Bv, Amsterdam., 150, 1-11.
https://doi.org/10.1016/j.jconhyd.2013.03.004

Jovic-Jovicic NP, Milutinović-Nikolić AD, Zunic MJ, Mojović ZD, Bankovic PT, Gržetić I, Jovanović DM. Synergic adsorption of Pb2+ and reactive dye-RB5 on two series of organomodified bentonites. in Journal of Contaminant Hydrology. 2013;150:1-11.
doi:10.1016/j.jconhyd.2013.03.004 .

Jovic-Jovicic, N. P., Milutinović-Nikolić, Aleksandra D., Zunic, M. J., Mojović, Zorica D., Bankovic, P. T., Gržetić, Ivan, Jovanović, Dušan M., "Synergic adsorption of Pb2+ and reactive dye-RB5 on two series of organomodified bentonites" in Journal of Contaminant Hydrology, 150 (2013):1-11,
https://doi.org/10.1016/j.jconhyd.2013.03.004 . .

TY  - JOUR
AU  - Zunic, Marija J.
AU  - Milutinović-Nikolić, Aleksandra D.
AU  - Jović-Jovičić, Nataša
AU  - Banković, Predrag
AU  - Mojović, Zorica D.
AU  - Manojlović, Dragan D.
AU  - Jovanović, Dušan M.
PY  - 2010
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1093
AB  - Modification and characterization of bentonite from location Bogovina, Serbia was performed in order to obtain material applicable in wastewater purification. The  lt 75 mu m bentonite fraction was used in organobentonite synthesis while the  lt 2 mu m bentonite fraction, obtained by hydroseparation was used in pillaring procedure. Organo-modification of bentonite was performed with (1-hexadecyl)trimethylammonium bromide (HDTMA-Br). Pillared bentonite was obtained using standard procedure. Al3+ and Fe3+ were incorporated in pillars in 4:1 ratio and applied as catalyst in catalytic wet peroxide oxidation. Differences in structure of starting and modified bentonites were established by XRD analysis and nitrogen physisorption on -196 degrees C. The (001) smectite peak around 2 theta = 6 degrees shifts during the modification process. The Na-exchange process lowered d(001) from 1.53 nm (2 theta = 5.78 degrees) for starting clay to 1.28 nm (2 theta = 6.92 degrees), but the clay retained its swelling properties. The pillaring process increased and fixed the basal spacing to 1.74 nm. Intercalation of HDTMA ions into smectite structure increased d(001) to 2.00 nm for organobentonite. Specific surface area, S-BET, was affected by particle size and type of modification. The samples with finer bentonite fraction had higher S-BET due to increased smectite content. Na-exchanged bentonite samples had higher S-BET value than starting clay samples of same granulation. Organomodification caused dramatic decrease in S-BET value, while the pillaring process lead to an increase of S-BET value. Adsorptive and catalytic purification of wastewaters containing dyes was tested using Acid Yellow 99 as a model dye. Na-exchanged bentonite had greater adsorption affinity for dye adsorption than raw bentonite owing to higher S-BET. By organomodification this affinity was enhanced more than 70 times due to transition of bentonite surface from hydrophilic to organophilic. Al,Fe pillared bentonite was proven to be efficient in catalytic wet peroxide oxidation of Acid Yellow 99 dye at room temperature.
AB  - Izvršena je modifikacija i karakterizacija bentonita radi dobijanja materijala za prečišćavanje otpadnih voda. Organo-modifikacija bentonita izvedena je pomoću heksadeciltrimetilamonijum-bromida. Pilareni bentonit dobijen je standardnim postupkom uz ugradnju Al3+ i Fe3+ jona u odnosu 4:1, i korišćen je kao katalizator za oksidativnu razgradnju u prisustvu vodonik-peroksida. Razlike u strukturi polaznog i modifikovanih bentonita utvrđene su rendgeno-strukturnom analizom i fizisorpcijom azota na -196°C. Ispitivano je adsorpciono i katalitičko prečišćavanje otpadnih voda koje sadrže boje, korišćenjem Acid Yellow 99 kao model boje. Izvršeno je poređenje katalitičkih i adsorpiconih svojstava modifikovanih bentonita.
PB  - Assoc Chemists & Chemical Engineers Of Serbia, Belgrade
T2  - Hemijska industrija
T1  - Modified Bentonite as Adsorbent and Catalyst for Purification of Wastewaters Containing Dyes
T1  - Modifikovani bentonit kao adsorbent i katalizator za prečišćavanje otpadnih voda koje sadrže boje
VL  - 64
IS  - 3
SP  - 193
EP  - 199
DO  - 10.2298/HEMIND091221023Z
ER  - 

@article{
author = "Zunic, Marija J. and Milutinović-Nikolić, Aleksandra D. and Jović-Jovičić, Nataša and Banković, Predrag and Mojović, Zorica D. and Manojlović, Dragan D. and Jovanović, Dušan M.",
year = "2010",
abstract = "Modification and characterization of bentonite from location Bogovina, Serbia was performed in order to obtain material applicable in wastewater purification. The  lt 75 mu m bentonite fraction was used in organobentonite synthesis while the  lt 2 mu m bentonite fraction, obtained by hydroseparation was used in pillaring procedure. Organo-modification of bentonite was performed with (1-hexadecyl)trimethylammonium bromide (HDTMA-Br). Pillared bentonite was obtained using standard procedure. Al3+ and Fe3+ were incorporated in pillars in 4:1 ratio and applied as catalyst in catalytic wet peroxide oxidation. Differences in structure of starting and modified bentonites were established by XRD analysis and nitrogen physisorption on -196 degrees C. The (001) smectite peak around 2 theta = 6 degrees shifts during the modification process. The Na-exchange process lowered d(001) from 1.53 nm (2 theta = 5.78 degrees) for starting clay to 1.28 nm (2 theta = 6.92 degrees), but the clay retained its swelling properties. The pillaring process increased and fixed the basal spacing to 1.74 nm. Intercalation of HDTMA ions into smectite structure increased d(001) to 2.00 nm for organobentonite. Specific surface area, S-BET, was affected by particle size and type of modification. The samples with finer bentonite fraction had higher S-BET due to increased smectite content. Na-exchanged bentonite samples had higher S-BET value than starting clay samples of same granulation. Organomodification caused dramatic decrease in S-BET value, while the pillaring process lead to an increase of S-BET value. Adsorptive and catalytic purification of wastewaters containing dyes was tested using Acid Yellow 99 as a model dye. Na-exchanged bentonite had greater adsorption affinity for dye adsorption than raw bentonite owing to higher S-BET. By organomodification this affinity was enhanced more than 70 times due to transition of bentonite surface from hydrophilic to organophilic. Al,Fe pillared bentonite was proven to be efficient in catalytic wet peroxide oxidation of Acid Yellow 99 dye at room temperature., Izvršena je modifikacija i karakterizacija bentonita radi dobijanja materijala za prečišćavanje otpadnih voda. Organo-modifikacija bentonita izvedena je pomoću heksadeciltrimetilamonijum-bromida. Pilareni bentonit dobijen je standardnim postupkom uz ugradnju Al3+ i Fe3+ jona u odnosu 4:1, i korišćen je kao katalizator za oksidativnu razgradnju u prisustvu vodonik-peroksida. Razlike u strukturi polaznog i modifikovanih bentonita utvrđene su rendgeno-strukturnom analizom i fizisorpcijom azota na -196°C. Ispitivano je adsorpciono i katalitičko prečišćavanje otpadnih voda koje sadrže boje, korišćenjem Acid Yellow 99 kao model boje. Izvršeno je poređenje katalitičkih i adsorpiconih svojstava modifikovanih bentonita.",
publisher = "Assoc Chemists & Chemical Engineers Of Serbia, Belgrade",
journal = "Hemijska industrija",
title = "Modified Bentonite as Adsorbent and Catalyst for Purification of Wastewaters Containing Dyes, Modifikovani bentonit kao adsorbent i katalizator za prečišćavanje otpadnih voda koje sadrže boje",
volume = "64",
number = "3",
pages = "193-199",
doi = "10.2298/HEMIND091221023Z"
}

Zunic, M. J., Milutinović-Nikolić, A. D., Jović-Jovičić, N., Banković, P., Mojović, Z. D., Manojlović, D. D.,& Jovanović, D. M.. (2010). Modified Bentonite as Adsorbent and Catalyst for Purification of Wastewaters Containing Dyes. in Hemijska industrija
Assoc Chemists & Chemical Engineers Of Serbia, Belgrade., 64(3), 193-199.
https://doi.org/10.2298/HEMIND091221023Z

Zunic MJ, Milutinović-Nikolić AD, Jović-Jovičić N, Banković P, Mojović ZD, Manojlović DD, Jovanović DM. Modified Bentonite as Adsorbent and Catalyst for Purification of Wastewaters Containing Dyes. in Hemijska industrija. 2010;64(3):193-199.
doi:10.2298/HEMIND091221023Z .

Zunic, Marija J., Milutinović-Nikolić, Aleksandra D., Jović-Jovičić, Nataša, Banković, Predrag, Mojović, Zorica D., Manojlović, Dragan D., Jovanović, Dušan M., "Modified Bentonite as Adsorbent and Catalyst for Purification of Wastewaters Containing Dyes" in Hemijska industrija, 64, no. 3 (2010):193-199,
https://doi.org/10.2298/HEMIND091221023Z . .

TY  - JOUR
AU  - Jovic-Jovicic, N.
AU  - Milutinović-Nikolić, Aleksandra D.
AU  - Bankovic, P.
AU  - Dojčinović, Biljana P.
AU  - Nedic, B.
AU  - Gržetić, Ivan
AU  - Jovanovic, D.
PY  - 2010
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1083
AB  - In this paper partial and complete substitution of cations in the interlayer region of clay with different amounts of two aliphatic ammonium cations was performed with aim of synthesis of organobentonites with multipurpose adsorption properties. Domestic clay from Bogovina was submitted according to a common procedure used for the obtention of organobentonite, which comprises the following steps: grinding, sieving, Na-exchange, cation exchange and drying. The samples were characterized by X-ray diffraction and infrared spectroscopy. The incorporation of surfactant molecules into smectite structure lead to constant increase of d(001) basal spacing. IR absorption bands assigned to methyl and methylene vibrations increased with the increase of surfactant/bentonite ratio and length of aliphatic chain in surfactant molecules. Adsorptive properties of the obtained materials were in accordance with their organophylicity: the adsorption of organic dye increased while the rate of removal of Pb2+ by adsorption decreased.
PB  - Polish Acad Sciences Inst Physics, Warsaw
T2  - Acta Physica Polonica. Series A: General Physics, Physics of Condensed Matter, Optics and Quantum El
T1  - Synthesis, Characterization and Adsorptive Properties of Organobentonites
VL  - 117
IS  - 5
SP  - 849
EP  - 854
DO  - 10.12693/APhysPolA.117.849
ER  - 

@article{
author = "Jovic-Jovicic, N. and Milutinović-Nikolić, Aleksandra D. and Bankovic, P. and Dojčinović, Biljana P. and Nedic, B. and Gržetić, Ivan and Jovanovic, D.",
year = "2010",
abstract = "In this paper partial and complete substitution of cations in the interlayer region of clay with different amounts of two aliphatic ammonium cations was performed with aim of synthesis of organobentonites with multipurpose adsorption properties. Domestic clay from Bogovina was submitted according to a common procedure used for the obtention of organobentonite, which comprises the following steps: grinding, sieving, Na-exchange, cation exchange and drying. The samples were characterized by X-ray diffraction and infrared spectroscopy. The incorporation of surfactant molecules into smectite structure lead to constant increase of d(001) basal spacing. IR absorption bands assigned to methyl and methylene vibrations increased with the increase of surfactant/bentonite ratio and length of aliphatic chain in surfactant molecules. Adsorptive properties of the obtained materials were in accordance with their organophylicity: the adsorption of organic dye increased while the rate of removal of Pb2+ by adsorption decreased.",
publisher = "Polish Acad Sciences Inst Physics, Warsaw",
journal = "Acta Physica Polonica. Series A: General Physics, Physics of Condensed Matter, Optics and Quantum El",
title = "Synthesis, Characterization and Adsorptive Properties of Organobentonites",
volume = "117",
number = "5",
pages = "849-854",
doi = "10.12693/APhysPolA.117.849"
}

Jovic-Jovicic, N., Milutinović-Nikolić, A. D., Bankovic, P., Dojčinović, B. P., Nedic, B., Gržetić, I.,& Jovanovic, D.. (2010). Synthesis, Characterization and Adsorptive Properties of Organobentonites. in Acta Physica Polonica. Series A: General Physics, Physics of Condensed Matter, Optics and Quantum El
Polish Acad Sciences Inst Physics, Warsaw., 117(5), 849-854.
https://doi.org/10.12693/APhysPolA.117.849

Jovic-Jovicic N, Milutinović-Nikolić AD, Bankovic P, Dojčinović BP, Nedic B, Gržetić I, Jovanovic D. Synthesis, Characterization and Adsorptive Properties of Organobentonites. in Acta Physica Polonica. Series A: General Physics, Physics of Condensed Matter, Optics and Quantum El. 2010;117(5):849-854.
doi:10.12693/APhysPolA.117.849 .

Jovic-Jovicic, N., Milutinović-Nikolić, Aleksandra D., Bankovic, P., Dojčinović, Biljana P., Nedic, B., Gržetić, Ivan, Jovanovic, D., "Synthesis, Characterization and Adsorptive Properties of Organobentonites" in Acta Physica Polonica. Series A: General Physics, Physics of Condensed Matter, Optics and Quantum El, 117, no. 5 (2010):849-854,
https://doi.org/10.12693/APhysPolA.117.849 . .

TY  - JOUR
AU  - Jovic-Jovicic, N.
AU  - Milutinović-Nikolić, Aleksandra D.
AU  - Bankovic, P.
AU  - Mojović, Zorica D.
AU  - Zunic, M.
AU  - Gržetić, Ivan
AU  - Jovanovic, D.
PY  - 2010
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1054
AB  - Partial substitution of the interlayer cations of a local bentonite (Bogovina) by hexadecyl trimethylammonium ions (HDTMA) was performed to prepare adsorbents able to simultaneously adsorb toxic metal cations and organic pollutants. Acid Orange 10 adsorption increased with increasing HDTMA addition, while the adsorption of Pb2+ decreased with increasing organophilicity. The adsorption of the dye and Pb2+ and their mixture onto Na-rich bentonite and HDTMA-bentonites, regardless of adsorbents' organophilicity, obeyed the pseudo-second-order kinetics model. (C) 2009 Elsevier B.V. All rights reserved.
PB  - Elsevier Science Bv, Amsterdam
T2  - Applied Clay Science
T1  - Organo-inorganic bentonite for simultaneous adsorption of Acid Orange 10 and lead ions
VL  - 47
IS  - 3-4
SP  - 452
EP  - 456
DO  - 10.1016/j.clay.2009.11.005
ER  - 

@article{
author = "Jovic-Jovicic, N. and Milutinović-Nikolić, Aleksandra D. and Bankovic, P. and Mojović, Zorica D. and Zunic, M. and Gržetić, Ivan and Jovanovic, D.",
year = "2010",
abstract = "Partial substitution of the interlayer cations of a local bentonite (Bogovina) by hexadecyl trimethylammonium ions (HDTMA) was performed to prepare adsorbents able to simultaneously adsorb toxic metal cations and organic pollutants. Acid Orange 10 adsorption increased with increasing HDTMA addition, while the adsorption of Pb2+ decreased with increasing organophilicity. The adsorption of the dye and Pb2+ and their mixture onto Na-rich bentonite and HDTMA-bentonites, regardless of adsorbents' organophilicity, obeyed the pseudo-second-order kinetics model. (C) 2009 Elsevier B.V. All rights reserved.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Applied Clay Science",
title = "Organo-inorganic bentonite for simultaneous adsorption of Acid Orange 10 and lead ions",
volume = "47",
number = "3-4",
pages = "452-456",
doi = "10.1016/j.clay.2009.11.005"
}

Jovic-Jovicic, N., Milutinović-Nikolić, A. D., Bankovic, P., Mojović, Z. D., Zunic, M., Gržetić, I.,& Jovanovic, D.. (2010). Organo-inorganic bentonite for simultaneous adsorption of Acid Orange 10 and lead ions. in Applied Clay Science
Elsevier Science Bv, Amsterdam., 47(3-4), 452-456.
https://doi.org/10.1016/j.clay.2009.11.005

Jovic-Jovicic N, Milutinović-Nikolić AD, Bankovic P, Mojović ZD, Zunic M, Gržetić I, Jovanovic D. Organo-inorganic bentonite for simultaneous adsorption of Acid Orange 10 and lead ions. in Applied Clay Science. 2010;47(3-4):452-456.
doi:10.1016/j.clay.2009.11.005 .

Jovic-Jovicic, N., Milutinović-Nikolić, Aleksandra D., Bankovic, P., Mojović, Zorica D., Zunic, M., Gržetić, Ivan, Jovanovic, D., "Organo-inorganic bentonite for simultaneous adsorption of Acid Orange 10 and lead ions" in Applied Clay Science, 47, no. 3-4 (2010):452-456,
https://doi.org/10.1016/j.clay.2009.11.005 . .

TY  - JOUR
AU  - Jović-Jovičić, Nataša
AU  - Milutinović-Nikolić, Aleksandra D.
AU  - Gržetić, Ivan
AU  - Banković, Predrag
AU  - Marković, Branislav Z.
AU  - Jovanović, Dušan M.
PY  - 2008
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/954
AB  - Natural bentonite clay from the Bogovina locality in Serbia was Na-exchanged and modified using hexadecyll-trimethylammonium bromide as surfactant and organobentonite was obtained. The influence of modifications on the structural, textural and sorption properties of bentonite was investigated. It was estimated that modifications solely replace exchangeable cations in smectite layers, whereas other admixture minerals (quartz, calcite, feldspar) in bentonite remain unaffected. According to X-ray results the modification lead to changes in the smectite structure by either decreasing, for Na-bentonite, or increasing, for organobentonite, the interplanar spacing, d(001). The appearance of three new bands in IR spectra of HDTMA-bentonite comparing to those of raw and Na-bentonite assigned to the methylene vibrations confirmed the embedding of aliphatic cations into smectite structure. In organobentonite a significant change in textural properties was observed. In particular, specific surface area dramatically decreased while originally meso and microporous material became almost completely non-porous. Despite almost insignificant specific surface area the synthesized organobentonite due to gained organophyllity of its surface exhibits exquisite adsorption properties toward investigated textile dyes having adsorption capacity approx. 2 times higher than activated carbon.
AB  - Prirodna bentonitna glina sa lokaliteta Bogovina u Srbiji je natrijumski izmenjena i modifikovana heksadeciltrimetil amonijum-bromidom kao surfaktantom, pri čemu je dobijen organobentonit. Ispitivan je uticaj modifikacije na strukturu, teksturalna i adsorpciona svojstva bentonita. Utvrđeno je da primenjeni postupci modifikacije dovode isključivo do izmene katjona u medulamelamom sloju smektita, dok modifikacija ne deluje na druge prateće minerale u bentonitu (kvare, kalcit, feldspat). Uprkos neznatnoj specifičnoj površini sintetizovani organobentonit zahvaljujući novodobijenoj organofilnosti površine pokazuje izuzetna adsorpciona svojstva prema tekstilnim bojama, imajući adsorpcioni kapacitet oko 2 puta veći od aktivnog uglja.
PB  - Assoc Chemical Engineers Serbia, Belgrade
T2  - Hemijska industrija
T1  - The influence of modification on structural, textural and adsorption properties of bentonite
T1  - Uticaj modifikacije na strukturna, teksturalna i adsorpciona svojstva bentonita
VL  - 62
IS  - 3
SP  - 131
EP  - 137
DO  - 10.2298/HEMIND0803131J
ER  - 

@article{
author = "Jović-Jovičić, Nataša and Milutinović-Nikolić, Aleksandra D. and Gržetić, Ivan and Banković, Predrag and Marković, Branislav Z. and Jovanović, Dušan M.",
year = "2008",
abstract = "Natural bentonite clay from the Bogovina locality in Serbia was Na-exchanged and modified using hexadecyll-trimethylammonium bromide as surfactant and organobentonite was obtained. The influence of modifications on the structural, textural and sorption properties of bentonite was investigated. It was estimated that modifications solely replace exchangeable cations in smectite layers, whereas other admixture minerals (quartz, calcite, feldspar) in bentonite remain unaffected. According to X-ray results the modification lead to changes in the smectite structure by either decreasing, for Na-bentonite, or increasing, for organobentonite, the interplanar spacing, d(001). The appearance of three new bands in IR spectra of HDTMA-bentonite comparing to those of raw and Na-bentonite assigned to the methylene vibrations confirmed the embedding of aliphatic cations into smectite structure. In organobentonite a significant change in textural properties was observed. In particular, specific surface area dramatically decreased while originally meso and microporous material became almost completely non-porous. Despite almost insignificant specific surface area the synthesized organobentonite due to gained organophyllity of its surface exhibits exquisite adsorption properties toward investigated textile dyes having adsorption capacity approx. 2 times higher than activated carbon., Prirodna bentonitna glina sa lokaliteta Bogovina u Srbiji je natrijumski izmenjena i modifikovana heksadeciltrimetil amonijum-bromidom kao surfaktantom, pri čemu je dobijen organobentonit. Ispitivan je uticaj modifikacije na strukturu, teksturalna i adsorpciona svojstva bentonita. Utvrđeno je da primenjeni postupci modifikacije dovode isključivo do izmene katjona u medulamelamom sloju smektita, dok modifikacija ne deluje na druge prateće minerale u bentonitu (kvare, kalcit, feldspat). Uprkos neznatnoj specifičnoj površini sintetizovani organobentonit zahvaljujući novodobijenoj organofilnosti površine pokazuje izuzetna adsorpciona svojstva prema tekstilnim bojama, imajući adsorpcioni kapacitet oko 2 puta veći od aktivnog uglja.",
publisher = "Assoc Chemical Engineers Serbia, Belgrade",
journal = "Hemijska industrija",
title = "The influence of modification on structural, textural and adsorption properties of bentonite, Uticaj modifikacije na strukturna, teksturalna i adsorpciona svojstva bentonita",
volume = "62",
number = "3",
pages = "131-137",
doi = "10.2298/HEMIND0803131J"
}

Jović-Jovičić, N., Milutinović-Nikolić, A. D., Gržetić, I., Banković, P., Marković, B. Z.,& Jovanović, D. M.. (2008). The influence of modification on structural, textural and adsorption properties of bentonite. in Hemijska industrija
Assoc Chemical Engineers Serbia, Belgrade., 62(3), 131-137.
https://doi.org/10.2298/HEMIND0803131J

Jović-Jovičić N, Milutinović-Nikolić AD, Gržetić I, Banković P, Marković BZ, Jovanović DM. The influence of modification on structural, textural and adsorption properties of bentonite. in Hemijska industrija. 2008;62(3):131-137.
doi:10.2298/HEMIND0803131J .

Jović-Jovičić, Nataša, Milutinović-Nikolić, Aleksandra D., Gržetić, Ivan, Banković, Predrag, Marković, Branislav Z., Jovanović, Dušan M., "The influence of modification on structural, textural and adsorption properties of bentonite" in Hemijska industrija, 62, no. 3 (2008):131-137,
https://doi.org/10.2298/HEMIND0803131J . .

TY  - JOUR
AU  - Jović-Jovičić, Nataša
AU  - Milutinović-Nikolić, Aleksandra D.
AU  - Gržetić, Ivan
AU  - Jovanović, Dušan
PY  - 2008
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/930
AB  - Domestic bentonite clay was modified using cationic surfactant - hexadecyltrimethylammonium bromide (HDTMA-bromide) in order to obtain more efficient sorbent. Removal of Acid Orange 10 from aqueous solution at different dye concentrations, adsorbent doses, and pH was studied. These studies were carried out under unaltered pH value in order to prove that adjusting pH as an additional operation in wastewater treatment is not entirely necessary. The results obtained confirmed the adsorption capacity is significant even for unaltered pH. The adsorption isotherm data were well fitted with both the Freundlich and Langmuir model and the latter was shown as more appropriate. Dynamical data were well represented with the pseudo second-order kinetic model. The results indicate that HDTMA-bentonite could be employed as low-cost sorbent in textile dye wastewater treatment.
PB  - Wiley-V C H Verlag Gmbh, Weinheim
T2  - Chemical Engineering and Technology
T1  - Organobentonite as efficient textile dye sorbent
VL  - 31
IS  - 4
SP  - 567
EP  - 574
DO  - 10.1002/ceat.200700421
ER  - 

@article{
author = "Jović-Jovičić, Nataša and Milutinović-Nikolić, Aleksandra D. and Gržetić, Ivan and Jovanović, Dušan",
year = "2008",
abstract = "Domestic bentonite clay was modified using cationic surfactant - hexadecyltrimethylammonium bromide (HDTMA-bromide) in order to obtain more efficient sorbent. Removal of Acid Orange 10 from aqueous solution at different dye concentrations, adsorbent doses, and pH was studied. These studies were carried out under unaltered pH value in order to prove that adjusting pH as an additional operation in wastewater treatment is not entirely necessary. The results obtained confirmed the adsorption capacity is significant even for unaltered pH. The adsorption isotherm data were well fitted with both the Freundlich and Langmuir model and the latter was shown as more appropriate. Dynamical data were well represented with the pseudo second-order kinetic model. The results indicate that HDTMA-bentonite could be employed as low-cost sorbent in textile dye wastewater treatment.",
publisher = "Wiley-V C H Verlag Gmbh, Weinheim",
journal = "Chemical Engineering and Technology",
title = "Organobentonite as efficient textile dye sorbent",
volume = "31",
number = "4",
pages = "567-574",
doi = "10.1002/ceat.200700421"
}

Jović-Jovičić, N., Milutinović-Nikolić, A. D., Gržetić, I.,& Jovanović, D.. (2008). Organobentonite as efficient textile dye sorbent. in Chemical Engineering and Technology
Wiley-V C H Verlag Gmbh, Weinheim., 31(4), 567-574.
https://doi.org/10.1002/ceat.200700421

Jović-Jovičić N, Milutinović-Nikolić AD, Gržetić I, Jovanović D. Organobentonite as efficient textile dye sorbent. in Chemical Engineering and Technology. 2008;31(4):567-574.
doi:10.1002/ceat.200700421 .

Jović-Jovičić, Nataša, Milutinović-Nikolić, Aleksandra D., Gržetić, Ivan, Jovanović, Dušan, "Organobentonite as efficient textile dye sorbent" in Chemical Engineering and Technology, 31, no. 4 (2008):567-574,
https://doi.org/10.1002/ceat.200700421 . .