TY  - JOUR
AU  - Sandić, Zvjezdana P.
AU  - Nastasović, Aleksandra
AU  - Jović-Jovičić, Nataša
AU  - Milutinović Nikolić, Aleksandra
AU  - Jovanović, Dušan M.
PY  - 2011
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/911
AB  - Macroporous poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate) (PGME) was synthesized by suspension copolymerization and functionalized with diethylene triamine (PGME-deta). The effect of pH, contact time, and sorbent mass on sorption efficiency of initial and functionalized copolymer sample for removal of Acid Orange 10 dye from aqueous solutions was studied. No dye was sorbed by nonfunctionalized copolymer, indicating that sorption of Acid Orange 10 by PGME-deta is specific, through amino groups. The isotherm data are best fitted by Langmuir model, indicating homogeneous distribution of active sites in PGME-deta as well as monolayer sorption. Sorption kinetics study showed that the sorption of Acid Orange 10 by PGME-deta obeys the pseudo-second-order kinetic model. It was shown that PGME-deta selectively sorbs Acid Orange 10 from binary solution with Bezaktiv Rot reactive dye. The comparison of sorption characteristics of PGME-deta with activated carbon showed that this functionalized copolymer might be used as an alternative sorbent for textile dyes.
PB  - Wiley-Blackwell, Malden
T2  - Journal of Applied Polymer Science
T1  - Sorption of Textile Dye from Aqueous Solution by Macroporous Amino-Functionalized Copolymer
VL  - 121
IS  - 1
SP  - 234
EP  - 242
DO  - 10.1002/app.33537
ER  - 

@article{
author = "Sandić, Zvjezdana P. and Nastasović, Aleksandra and Jović-Jovičić, Nataša and Milutinović Nikolić, Aleksandra and Jovanović, Dušan M.",
year = "2011",
abstract = "Macroporous poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate) (PGME) was synthesized by suspension copolymerization and functionalized with diethylene triamine (PGME-deta). The effect of pH, contact time, and sorbent mass on sorption efficiency of initial and functionalized copolymer sample for removal of Acid Orange 10 dye from aqueous solutions was studied. No dye was sorbed by nonfunctionalized copolymer, indicating that sorption of Acid Orange 10 by PGME-deta is specific, through amino groups. The isotherm data are best fitted by Langmuir model, indicating homogeneous distribution of active sites in PGME-deta as well as monolayer sorption. Sorption kinetics study showed that the sorption of Acid Orange 10 by PGME-deta obeys the pseudo-second-order kinetic model. It was shown that PGME-deta selectively sorbs Acid Orange 10 from binary solution with Bezaktiv Rot reactive dye. The comparison of sorption characteristics of PGME-deta with activated carbon showed that this functionalized copolymer might be used as an alternative sorbent for textile dyes.",
publisher = "Wiley-Blackwell, Malden",
journal = "Journal of Applied Polymer Science",
title = "Sorption of Textile Dye from Aqueous Solution by Macroporous Amino-Functionalized Copolymer",
volume = "121",
number = "1",
pages = "234-242",
doi = "10.1002/app.33537"
}

Sandić, Z. P., Nastasović, A., Jović-Jovičić, N., Milutinović Nikolić, A.,& Jovanović, D. M.. (2011). Sorption of Textile Dye from Aqueous Solution by Macroporous Amino-Functionalized Copolymer. in Journal of Applied Polymer Science
Wiley-Blackwell, Malden., 121(1), 234-242.
https://doi.org/10.1002/app.33537

Sandić ZP, Nastasović A, Jović-Jovičić N, Milutinović Nikolić A, Jovanović DM. Sorption of Textile Dye from Aqueous Solution by Macroporous Amino-Functionalized Copolymer. in Journal of Applied Polymer Science. 2011;121(1):234-242.
doi:10.1002/app.33537 .

Sandić, Zvjezdana P., Nastasović, Aleksandra, Jović-Jovičić, Nataša, Milutinović Nikolić, Aleksandra, Jovanović, Dušan M., "Sorption of Textile Dye from Aqueous Solution by Macroporous Amino-Functionalized Copolymer" in Journal of Applied Polymer Science, 121, no. 1 (2011):234-242,
https://doi.org/10.1002/app.33537 . .

TY  - JOUR
AU  - Mojović, Zorica
AU  - Jović-Jovičić, Nataša
AU  - Banković, Predrag
AU  - Žunić, Marija
AU  - Abu Rabi-Stanković, Andjela S.
AU  - Milutinović Nikolić, Aleksandra
AU  - Jovanović, Dušan M.
PY  - 2011
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/840
AB  - Bentonite was modified by the exchange of inorganic cations with hexadecyl trimethylammonium, dodecyl trimethylammonium or tetramethylammonium cation. The obtained materials were characterized by physisorption of nitrogen and X-ray diffraction analysis. Multisweep cyclic voltammetry was applied to analyze phenol response on different organo bentonite-based electrodes. The aim of the investigation was to determine the influence of the type of modifying agent on the electrochemical performance of the investigated electrodes. All electrodes exhibited similar electrochemical behavior but with different intensities of the electrochemical response and Tafel slopes. The difference in Tafel slopes reflected different level of involvement of pores in the phenol electrooxidation.
PB  - Elsevier
T2  - Applied Clay Science
T1  - Electrooxidation of phenol on different organo bentonite-based electrodes
VL  - 53
IS  - 2
SP  - 331
EP  - 335
DO  - 10.1016/j.clay.2010.12.008
ER  - 

@article{
author = "Mojović, Zorica and Jović-Jovičić, Nataša and Banković, Predrag and Žunić, Marija and Abu Rabi-Stanković, Andjela S. and Milutinović Nikolić, Aleksandra and Jovanović, Dušan M.",
year = "2011",
abstract = "Bentonite was modified by the exchange of inorganic cations with hexadecyl trimethylammonium, dodecyl trimethylammonium or tetramethylammonium cation. The obtained materials were characterized by physisorption of nitrogen and X-ray diffraction analysis. Multisweep cyclic voltammetry was applied to analyze phenol response on different organo bentonite-based electrodes. The aim of the investigation was to determine the influence of the type of modifying agent on the electrochemical performance of the investigated electrodes. All electrodes exhibited similar electrochemical behavior but with different intensities of the electrochemical response and Tafel slopes. The difference in Tafel slopes reflected different level of involvement of pores in the phenol electrooxidation.",
publisher = "Elsevier",
journal = "Applied Clay Science",
title = "Electrooxidation of phenol on different organo bentonite-based electrodes",
volume = "53",
number = "2",
pages = "331-335",
doi = "10.1016/j.clay.2010.12.008"
}

Mojović, Z., Jović-Jovičić, N., Banković, P., Žunić, M., Abu Rabi-Stanković, A. S., Milutinović Nikolić, A.,& Jovanović, D. M.. (2011). Electrooxidation of phenol on different organo bentonite-based electrodes. in Applied Clay Science
Elsevier., 53(2), 331-335.
https://doi.org/10.1016/j.clay.2010.12.008

Mojović Z, Jović-Jovičić N, Banković P, Žunić M, Abu Rabi-Stanković AS, Milutinović Nikolić A, Jovanović DM. Electrooxidation of phenol on different organo bentonite-based electrodes. in Applied Clay Science. 2011;53(2):331-335.
doi:10.1016/j.clay.2010.12.008 .

Mojović, Zorica, Jović-Jovičić, Nataša, Banković, Predrag, Žunić, Marija, Abu Rabi-Stanković, Andjela S., Milutinović Nikolić, Aleksandra, Jovanović, Dušan M., "Electrooxidation of phenol on different organo bentonite-based electrodes" in Applied Clay Science, 53, no. 2 (2011):331-335,
https://doi.org/10.1016/j.clay.2010.12.008 . .

TY  - JOUR
AU  - Dostanić, Jasmina
AU  - Lončarević, Davor
AU  - Banković, Predrag
AU  - Cvetković, Olga
AU  - Jovanović, Dušan M.
AU  - Mijin, Dušan
PY  - 2011
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/920
AB  - Photocatalytic degradation of synthesized azo pyridone dye (5-(4-sulpho phenylazo)-6-hydroxy-4-methyl-3-cyano-2-pyridone), in aqueous solutions by simulated sunlight in the presence of commercial TiO2, Aeroxide P25, was studied. The reaction kinetics analysis showed that photodegradation exhibits pseudo first-order kinetics according to Langmuir-Hinshelwood model. The effects of various process parameters on the photocatalytic degradation were investigated. The optimal catalyst content and pH were determined. A decrease in the reaction rate was observed upon the increase of the initial dye concentration. Degradation of the dye was enhanced by hydrogen peroxide, but it was inhibited by ethanol. The influence of temperature was studied, and the energy of activation was determined. According to total organic carbon (TOC) analysis, 54% of TOC remained when 100% of the dye was decolorized. Although the intermediates were not determined in this study, the TOC results clearly indicate their presence during the reaction. In addition, photocatalytic degradation of simulated dyehouse effluents, containing tested azo pyridone dye and associated auxiliary chemicals was investigated.
PB  - Taylor and Francis Inc.
T2  - Journal of Environmental Science and Health - Part A Toxic/Hazardous Substances and Environmental En
T1  - Influence of process parameters on the photodegradation of synthesized azo pyridone dye in TiO2 water suspension under simulated sunlight
VL  - 46
IS  - 1
SP  - 70
EP  - 79
DO  - 10.1080/10934529.2011.526905
ER  - 

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

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

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

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

TY  - JOUR
AU  - Nikolova, Dimitrinka
AU  - Krstić, Jugoslav
AU  - Spasov, L.
AU  - Simeonov, D.
AU  - Lončarević, Davor
AU  - Stefanov, Pl.
AU  - Jovanović, Dušan M.
PY  - 2011
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/811
AB  - The effect of the type of the silica gel pore structure on the surface properties of the Ni-silica gel catalyst precursors for the vegetable oil hydrogenation process has been examined applying N-2 sorption and X-ray photoelectron spectroscopy techniques. The nickel catalyst precursors with identical composition (SiO2/Ni = 1.0) has been synthesized by precipitation of Ni(NO3)(2) center dot 6H(2)O solution with Na2CO3 solution on the three types of silica gel with different pore structures. It is shown that the usage of the silica gel supports with different texture as source of SiO2 causes different location of Ni-species into the support pores and on the external surface area. The XPS data confirm the formation of surface species with different strength of interaction and different dispersion. These surface characteristics of the precursors will predetermine the formation of the active nickel metallic phase as well as the mass transfer of the reactants and products to and from the catalytic sites.
PB  - Maik Nauka/Interperiodica/Springer, New York
T2  - Russian Journal of Physical Chemistry A
T1  - Surface properties of the Ni-silica gel catalyst precursors for the vegetable oil hydrogenation process: N-2 sorption and XPS studies
VL  - 85
IS  - 13
SP  - 2380
EP  - 2385
DO  - 10.1134/S0036024411130188
ER  - 

@article{
author = "Nikolova, Dimitrinka and Krstić, Jugoslav and Spasov, L. and Simeonov, D. and Lončarević, Davor and Stefanov, Pl. and Jovanović, Dušan M.",
year = "2011",
abstract = "The effect of the type of the silica gel pore structure on the surface properties of the Ni-silica gel catalyst precursors for the vegetable oil hydrogenation process has been examined applying N-2 sorption and X-ray photoelectron spectroscopy techniques. The nickel catalyst precursors with identical composition (SiO2/Ni = 1.0) has been synthesized by precipitation of Ni(NO3)(2) center dot 6H(2)O solution with Na2CO3 solution on the three types of silica gel with different pore structures. It is shown that the usage of the silica gel supports with different texture as source of SiO2 causes different location of Ni-species into the support pores and on the external surface area. The XPS data confirm the formation of surface species with different strength of interaction and different dispersion. These surface characteristics of the precursors will predetermine the formation of the active nickel metallic phase as well as the mass transfer of the reactants and products to and from the catalytic sites.",
publisher = "Maik Nauka/Interperiodica/Springer, New York",
journal = "Russian Journal of Physical Chemistry A",
title = "Surface properties of the Ni-silica gel catalyst precursors for the vegetable oil hydrogenation process: N-2 sorption and XPS studies",
volume = "85",
number = "13",
pages = "2380-2385",
doi = "10.1134/S0036024411130188"
}

Nikolova, D., Krstić, J., Spasov, L., Simeonov, D., Lončarević, D., Stefanov, Pl.,& Jovanović, D. M.. (2011). Surface properties of the Ni-silica gel catalyst precursors for the vegetable oil hydrogenation process: N-2 sorption and XPS studies. in Russian Journal of Physical Chemistry A
Maik Nauka/Interperiodica/Springer, New York., 85(13), 2380-2385.
https://doi.org/10.1134/S0036024411130188

Nikolova D, Krstić J, Spasov L, Simeonov D, Lončarević D, Stefanov P, Jovanović DM. Surface properties of the Ni-silica gel catalyst precursors for the vegetable oil hydrogenation process: N-2 sorption and XPS studies. in Russian Journal of Physical Chemistry A. 2011;85(13):2380-2385.
doi:10.1134/S0036024411130188 .

Nikolova, Dimitrinka, Krstić, Jugoslav, Spasov, L., Simeonov, D., Lončarević, Davor, Stefanov, Pl., Jovanović, Dušan M., "Surface properties of the Ni-silica gel catalyst precursors for the vegetable oil hydrogenation process: N-2 sorption and XPS studies" in Russian Journal of Physical Chemistry A, 85, no. 13 (2011):2380-2385,
https://doi.org/10.1134/S0036024411130188 . .

TY  - JOUR
AU  - Gabrovska, Margarita
AU  - Krstić, Jugoslav
AU  - Tzvetkov, P.
AU  - Tenchev, K.
AU  - Shopska, M.
AU  - Vukelić, Nikola
AU  - Jovanović, Dušan M.
PY  - 2011
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/829
AB  - Ni/SiO(2) materials with identical composition (SiO(2)/Ni = 1.0) have been synthesized by precipitation of Ni(NO(3))(2) center dot 6H(2)O solution with Na(2)CO(3) solution on the silica gel, obtained at three different pH values. The present investigation was undertaken in an endeavor to study the effects of the silica gel support type and the reduction temperature on the formation and dispersion of the metallic nickel phase in the reduced Ni/SiO(2) precursors of the vegetable oil hydrogenation catalyst. The physicochemical characterization of the unreduced and reduced precursors has been accomplished appropriately by powder X-ray diffraction, infrared spectroscopy, temperature programmed reduction and H(2)-chemisorption techniques. It can be stated that the texture peculiarities of the silica gels used as supports influence on the crystalline state and distribution of the deposited Ni-containing phases during the preparation of the precursors, on the reduction temperature of the investigated solids as well as on the bulk size and surface dispersion of the arising metallic nickel particles. It was shown that two types of Ni(2+)-species are formed during the synthesis procedure, namely basic nickel carbonate-like and Ni-phyllosilicate with different extent of presence, location and strength of interaction. The different location of these species is supposed to result in various strength of Ni-O and Ni-O-Si interaction, thus determining the overall reducibility of the precursors. It was specified that the Ni(2+)-species are strongly bonded to the surface of the silica gel obtained at neutral pH value and weakly bonded to the surface of those prepared in acidic and alkaline conditions. It was established that the precursor, derivates from the silica gel obtained at alkaline conditions, demonstrates both significant reduction of the Ni2+ ions at 430A degrees C and finely dispersed metallic nickel particles on its surface. High dispersion of the metallic nickel might be the crucial reason for achieving of high activity in the vegetable oil hydrogenation.
PB  - Maik Nauka/Interperiodica/Springer, New York
T2  - Russian Journal of Physical Chemistry A
T1  - Effect of the support and the reduction temperature on the formation of metallic nickel phase in Ni/silica gel precursors of vegetable oil hydrogenation catalysts
VL  - 85
IS  - 13
SP  - 2392
EP  - 2398
DO  - 10.1134/S0036024411130073
ER  - 

@article{
author = "Gabrovska, Margarita and Krstić, Jugoslav and Tzvetkov, P. and Tenchev, K. and Shopska, M. and Vukelić, Nikola and Jovanović, Dušan M.",
year = "2011",
abstract = "Ni/SiO(2) materials with identical composition (SiO(2)/Ni = 1.0) have been synthesized by precipitation of Ni(NO(3))(2) center dot 6H(2)O solution with Na(2)CO(3) solution on the silica gel, obtained at three different pH values. The present investigation was undertaken in an endeavor to study the effects of the silica gel support type and the reduction temperature on the formation and dispersion of the metallic nickel phase in the reduced Ni/SiO(2) precursors of the vegetable oil hydrogenation catalyst. The physicochemical characterization of the unreduced and reduced precursors has been accomplished appropriately by powder X-ray diffraction, infrared spectroscopy, temperature programmed reduction and H(2)-chemisorption techniques. It can be stated that the texture peculiarities of the silica gels used as supports influence on the crystalline state and distribution of the deposited Ni-containing phases during the preparation of the precursors, on the reduction temperature of the investigated solids as well as on the bulk size and surface dispersion of the arising metallic nickel particles. It was shown that two types of Ni(2+)-species are formed during the synthesis procedure, namely basic nickel carbonate-like and Ni-phyllosilicate with different extent of presence, location and strength of interaction. The different location of these species is supposed to result in various strength of Ni-O and Ni-O-Si interaction, thus determining the overall reducibility of the precursors. It was specified that the Ni(2+)-species are strongly bonded to the surface of the silica gel obtained at neutral pH value and weakly bonded to the surface of those prepared in acidic and alkaline conditions. It was established that the precursor, derivates from the silica gel obtained at alkaline conditions, demonstrates both significant reduction of the Ni2+ ions at 430A degrees C and finely dispersed metallic nickel particles on its surface. High dispersion of the metallic nickel might be the crucial reason for achieving of high activity in the vegetable oil hydrogenation.",
publisher = "Maik Nauka/Interperiodica/Springer, New York",
journal = "Russian Journal of Physical Chemistry A",
title = "Effect of the support and the reduction temperature on the formation of metallic nickel phase in Ni/silica gel precursors of vegetable oil hydrogenation catalysts",
volume = "85",
number = "13",
pages = "2392-2398",
doi = "10.1134/S0036024411130073"
}

Gabrovska, M., Krstić, J., Tzvetkov, P., Tenchev, K., Shopska, M., Vukelić, N.,& Jovanović, D. M.. (2011). Effect of the support and the reduction temperature on the formation of metallic nickel phase in Ni/silica gel precursors of vegetable oil hydrogenation catalysts. in Russian Journal of Physical Chemistry A
Maik Nauka/Interperiodica/Springer, New York., 85(13), 2392-2398.
https://doi.org/10.1134/S0036024411130073

Gabrovska M, Krstić J, Tzvetkov P, Tenchev K, Shopska M, Vukelić N, Jovanović DM. Effect of the support and the reduction temperature on the formation of metallic nickel phase in Ni/silica gel precursors of vegetable oil hydrogenation catalysts. in Russian Journal of Physical Chemistry A. 2011;85(13):2392-2398.
doi:10.1134/S0036024411130073 .

Gabrovska, Margarita, Krstić, Jugoslav, Tzvetkov, P., Tenchev, K., Shopska, M., Vukelić, Nikola, Jovanović, Dušan M., "Effect of the support and the reduction temperature on the formation of metallic nickel phase in Ni/silica gel precursors of vegetable oil hydrogenation catalysts" in Russian Journal of Physical Chemistry A, 85, no. 13 (2011):2392-2398,
https://doi.org/10.1134/S0036024411130073 . .

TY  - CONF
AU  - Jović-Jovičić, Nataša
AU  - Žunić, Marija
AU  - Banković, Predrag
AU  - Mojović, Zorica
AU  - Milutinović Nikolić, Aleksandra
AU  - Dojčinović, Biljana
AU  - Gržetić, Ivan
PY  - 2010
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/6637
AB  - Quantitative substitution of the interlayer cations of smectite by hexadecyl trimethylammonium ions (HDTMA) was performed in order to prepare adsorbent able to simultaneously adsorb toxic metal cations and organic pollutants. The adsorption of Acid Yellow 99 textile dye and Pb2+ ion from their single solutions and mixture was performed. Kinetic data of adsorption were well represented by pseudo-second-order kinetic model for all investigated adsorption systems.
PB  - Society of Physical Chemists of Serbia
C3  - Proceedings - X International Conference on fundamental and applied aspects of Physical chemistry, 21-24 September 2010, Belgrade
T1  - Kinetics of adsorption of mixed pollutants by organobentonite
VL  - I
SP  - 173
EP  - 175
UR  - https://hdl.handle.net/21.15107/rcub_cer_6637
ER  - 

@conference{
author = "Jović-Jovičić, Nataša and Žunić, Marija and Banković, Predrag and Mojović, Zorica and Milutinović Nikolić, Aleksandra and Dojčinović, Biljana and Gržetić, Ivan",
year = "2010",
abstract = "Quantitative substitution of the interlayer cations of smectite by hexadecyl trimethylammonium ions (HDTMA) was performed in order to prepare adsorbent able to simultaneously adsorb toxic metal cations and organic pollutants. The adsorption of Acid Yellow 99 textile dye and Pb2+ ion from their single solutions and mixture was performed. Kinetic data of adsorption were well represented by pseudo-second-order kinetic model for all investigated adsorption systems.",
publisher = "Society of Physical Chemists of Serbia",
journal = "Proceedings - X International Conference on fundamental and applied aspects of Physical chemistry, 21-24 September 2010, Belgrade",
title = "Kinetics of adsorption of mixed pollutants by organobentonite",
volume = "I",
pages = "173-175",
url = "https://hdl.handle.net/21.15107/rcub_cer_6637"
}

Jović-Jovičić, N., Žunić, M., Banković, P., Mojović, Z., Milutinović Nikolić, A., Dojčinović, B.,& Gržetić, I.. (2010). Kinetics of adsorption of mixed pollutants by organobentonite. in Proceedings - X International Conference on fundamental and applied aspects of Physical chemistry, 21-24 September 2010, Belgrade
Society of Physical Chemists of Serbia., I, 173-175.
https://hdl.handle.net/21.15107/rcub_cer_6637

Jović-Jovičić N, Žunić M, Banković P, Mojović Z, Milutinović Nikolić A, Dojčinović B, Gržetić I. Kinetics of adsorption of mixed pollutants by organobentonite. in Proceedings - X International Conference on fundamental and applied aspects of Physical chemistry, 21-24 September 2010, Belgrade. 2010;I:173-175.
https://hdl.handle.net/21.15107/rcub_cer_6637 .

Jović-Jovičić, Nataša, Žunić, Marija, Banković, Predrag, Mojović, Zorica, Milutinović Nikolić, Aleksandra, Dojčinović, Biljana, Gržetić, Ivan, "Kinetics of adsorption of mixed pollutants by organobentonite" in Proceedings - X International Conference on fundamental and applied aspects of Physical chemistry, 21-24 September 2010, Belgrade, I (2010):173-175,
https://hdl.handle.net/21.15107/rcub_cer_6637 .

TY  - CONF
AU  - Banković, Predrag
AU  - Milutinović Nikolić, Aleksandra
AU  - Mojović, Zorica
AU  - Jović-Jovičić, Nataša
AU  - Žunić, Marija
AU  - Dondur, Vera
AU  - Jovanović, Dušan
PY  - 2010
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/6684
AB  - Al,Fe-pillared clays (PILCs) have shown good performance in catalytic wet 
peroxide oxidation (CWPO) of organic pollutants in water. They have predominantly 
been tested in the degradation of phenol. There are seldom reports on their use in 
the degradation of other organic pollutants such as toluene and dyes. In this 
work a series of Al,Fe–PILCs with different Fe3+ content was synthesized and 
characterized. Their catalytic performance was studied in the CWPO of food dye 
tartrazine used as a model compound. Degree of decolorization of tartrazine 
containing aqueous solution was monitored in relation to different parameters such 
as Fe3+ content and temperature.
PB  - Novosibirsk, Russia : Boreskov Institute of Catalysis SB RAS
C3  - XIX International Conference on Chemical Reactors "CHEMREACTOR-19", Abstracts, September 5-9, Novosibirsk
T1  - Al, Fe-pillared clays in catalytic decolorization of dye containing water
SP  - 450
EP  - 451
UR  - https://hdl.handle.net/21.15107/rcub_cer_6684
ER  - 

@conference{
author = "Banković, Predrag and Milutinović Nikolić, Aleksandra and Mojović, Zorica and Jović-Jovičić, Nataša and Žunić, Marija and Dondur, Vera and Jovanović, Dušan",
year = "2010",
abstract = "Al,Fe-pillared clays (PILCs) have shown good performance in catalytic wet 
peroxide oxidation (CWPO) of organic pollutants in water. They have predominantly 
been tested in the degradation of phenol. There are seldom reports on their use in 
the degradation of other organic pollutants such as toluene and dyes. In this 
work a series of Al,Fe–PILCs with different Fe3+ content was synthesized and 
characterized. Their catalytic performance was studied in the CWPO of food dye 
tartrazine used as a model compound. Degree of decolorization of tartrazine 
containing aqueous solution was monitored in relation to different parameters such 
as Fe3+ content and temperature.",
publisher = "Novosibirsk, Russia : Boreskov Institute of Catalysis SB RAS",
journal = "XIX International Conference on Chemical Reactors "CHEMREACTOR-19", Abstracts, September 5-9, Novosibirsk",
title = "Al, Fe-pillared clays in catalytic decolorization of dye containing water",
pages = "450-451",
url = "https://hdl.handle.net/21.15107/rcub_cer_6684"
}

Banković, P., Milutinović Nikolić, A., Mojović, Z., Jović-Jovičić, N., Žunić, M., Dondur, V.,& Jovanović, D.. (2010). Al, Fe-pillared clays in catalytic decolorization of dye containing water. in XIX International Conference on Chemical Reactors "CHEMREACTOR-19", Abstracts, September 5-9, Novosibirsk
Novosibirsk, Russia : Boreskov Institute of Catalysis SB RAS., 450-451.
https://hdl.handle.net/21.15107/rcub_cer_6684

Banković P, Milutinović Nikolić A, Mojović Z, Jović-Jovičić N, Žunić M, Dondur V, Jovanović D. Al, Fe-pillared clays in catalytic decolorization of dye containing water. in XIX International Conference on Chemical Reactors "CHEMREACTOR-19", Abstracts, September 5-9, Novosibirsk. 2010;:450-451.
https://hdl.handle.net/21.15107/rcub_cer_6684 .

Banković, Predrag, Milutinović Nikolić, Aleksandra, Mojović, Zorica, Jović-Jovičić, Nataša, Žunić, Marija, Dondur, Vera, Jovanović, Dušan, "Al, Fe-pillared clays in catalytic decolorization of dye containing water" in XIX International Conference on Chemical Reactors "CHEMREACTOR-19", Abstracts, September 5-9, Novosibirsk (2010):450-451,
https://hdl.handle.net/21.15107/rcub_cer_6684 .

TY  - JOUR
AU  - Mojović, Miloš
AU  - Dakovic, Marko
AU  - Omerasevic, Mia
AU  - Mojović, Zorica
AU  - Banković, Predrag
AU  - Milutinović Nikolić, Aleksandra
AU  - Jovanović, Dušan M.
PY  - 2010
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/648
AB  - The increased use of imaging techniques in diagnostic studies, such as MRI, has contributed to the development of the wide range of new materials which could be successfully used as image improving agents. However, there is a lack of such substances in the area of gastrointestinal tract MRI. Many of the traditionally popular relaxation altering agents show poor results and disadvantages provoking black bowel, side effects of diarrhea and the presence of artifacts arising from clumping. Paramagnetic species seem to be potentially suitable agents for these studies, but contrast opacification has been reported and less than 60% of the gastrointestinal tract magnetic resonance scans showed improved delineation of abdominal pathologies. The new solution has been proposed as zeolites or smectite clays (hectorite and montmorillonite) enclosing of paramagnetic metal ions obtained by ion-exchange methods. However, such materials have problems of leakage of paramagnetic ions causing the appearance of the various side-effects. In this study we show that Co(+2) and Dy(+3) paramagnetic-pillared bentonites could be successfully used as MRI digestive tract non-leaching contrast agents, altering the longitudinal and transverse relaxation times of fluids in contact with the clay minerals.
PB  - World Scientific Publ Co Pte Ltd, Singapore
T2  - International Journal of Modern Physics B
T1  - The paramagnetic pillared bentonites as digestive tract mri contrast agents
VL  - 24
IS  - 6-7
SP  - 780
EP  - 787
DO  - 10.1142/S0217979210064411
ER  - 

@article{
author = "Mojović, Miloš and Dakovic, Marko and Omerasevic, Mia and Mojović, Zorica and Banković, Predrag and Milutinović Nikolić, Aleksandra and Jovanović, Dušan M.",
year = "2010",
abstract = "The increased use of imaging techniques in diagnostic studies, such as MRI, has contributed to the development of the wide range of new materials which could be successfully used as image improving agents. However, there is a lack of such substances in the area of gastrointestinal tract MRI. Many of the traditionally popular relaxation altering agents show poor results and disadvantages provoking black bowel, side effects of diarrhea and the presence of artifacts arising from clumping. Paramagnetic species seem to be potentially suitable agents for these studies, but contrast opacification has been reported and less than 60% of the gastrointestinal tract magnetic resonance scans showed improved delineation of abdominal pathologies. The new solution has been proposed as zeolites or smectite clays (hectorite and montmorillonite) enclosing of paramagnetic metal ions obtained by ion-exchange methods. However, such materials have problems of leakage of paramagnetic ions causing the appearance of the various side-effects. In this study we show that Co(+2) and Dy(+3) paramagnetic-pillared bentonites could be successfully used as MRI digestive tract non-leaching contrast agents, altering the longitudinal and transverse relaxation times of fluids in contact with the clay minerals.",
publisher = "World Scientific Publ Co Pte Ltd, Singapore",
journal = "International Journal of Modern Physics B",
title = "The paramagnetic pillared bentonites as digestive tract mri contrast agents",
volume = "24",
number = "6-7",
pages = "780-787",
doi = "10.1142/S0217979210064411"
}

Mojović, M., Dakovic, M., Omerasevic, M., Mojović, Z., Banković, P., Milutinović Nikolić, A.,& Jovanović, D. M.. (2010). The paramagnetic pillared bentonites as digestive tract mri contrast agents. in International Journal of Modern Physics B
World Scientific Publ Co Pte Ltd, Singapore., 24(6-7), 780-787.
https://doi.org/10.1142/S0217979210064411

Mojović M, Dakovic M, Omerasevic M, Mojović Z, Banković P, Milutinović Nikolić A, Jovanović DM. The paramagnetic pillared bentonites as digestive tract mri contrast agents. in International Journal of Modern Physics B. 2010;24(6-7):780-787.
doi:10.1142/S0217979210064411 .

Mojović, Miloš, Dakovic, Marko, Omerasevic, Mia, Mojović, Zorica, Banković, Predrag, Milutinović Nikolić, Aleksandra, Jovanović, Dušan M., "The paramagnetic pillared bentonites as digestive tract mri contrast agents" in International Journal of Modern Physics B, 24, no. 6-7 (2010):780-787,
https://doi.org/10.1142/S0217979210064411 . .

TY  - JOUR
AU  - Mojović, Miloš
AU  - Dakovic, Marko
AU  - Banković, Predrag
AU  - Mojović, Zorica
PY  - 2010
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/652
AB  - The availability of sophisticated diagnostic methods such as MRI has contributed to the increased use of imaging technologies in therapy and diagnostic studies. However, gastrointestinal tract MRI generally shows poor results because of the lack of suitable contrast agents. The iron oxide is traditionally popular material for MRI gastrointestinal studies because of its well-known superparamagnetic properties. On the other hand, it has many disadvantages which include black bowel, side effects of diarrhea and, from an important analytical standpoint, the presence of artifacts arising from clumping. When paramagnetic iron concentrates, it may become ferromagnetic, drastically altering its imaging properties. Other paramagnetic species, represented by gadolinium, also seem to be potentially suitable agents for these studies. Nevertheless, this metal itself cannot be used in humans because of its toxic properties. Therefore, there is clearly a need for orally effective, well tolerated agents that can be used in humans for digestive imaging studies. This MRI contrast should be useful for visualizing the anatomy of the digestive tract and particularly to differentiate between normal and pathological states, such as tumors. The solution has been proposed as zeolites or smectites (hectorite and montmorillonite) enclosing of paramagnetic metal ions obtained by ion-exchange methods. However, such materials could have problems of leakage of paramagnetic ions causing the appearance of the number side-effects. We propose the usage of the pillaring method for paramagnetic metal encapsulation in bentonites. By that way, paramagnetic cations like Fe(+3), Mn(+2) and Gd(+3) are introduced between clay mineral layers as polyoxo cations. After calcination, these polyoxo cations grow to be pillars (oxides of these metals) which are incorporated into the clay mineral matrix which prevents ion-leaching and dangerous side-effects. In this study we show that paramagnetic-pillared bentonites could be successfully used as MRI digestive tract non-leaching contrast agents, altering the longitudinal relaxation times of fluids in contact with the clay minerals.
PB  - Elsevier
T2  - Applied Clay Science
T1  - Paramagnetic pillared bentonites - The new digestive tract MRI contrast agents
VL  - 48
IS  - 1-2
SP  - 191
EP  - 194
DO  - 10.1016/j.clay.2009.11.041
ER  - 

@article{
author = "Mojović, Miloš and Dakovic, Marko and Banković, Predrag and Mojović, Zorica",
year = "2010",
abstract = "The availability of sophisticated diagnostic methods such as MRI has contributed to the increased use of imaging technologies in therapy and diagnostic studies. However, gastrointestinal tract MRI generally shows poor results because of the lack of suitable contrast agents. The iron oxide is traditionally popular material for MRI gastrointestinal studies because of its well-known superparamagnetic properties. On the other hand, it has many disadvantages which include black bowel, side effects of diarrhea and, from an important analytical standpoint, the presence of artifacts arising from clumping. When paramagnetic iron concentrates, it may become ferromagnetic, drastically altering its imaging properties. Other paramagnetic species, represented by gadolinium, also seem to be potentially suitable agents for these studies. Nevertheless, this metal itself cannot be used in humans because of its toxic properties. Therefore, there is clearly a need for orally effective, well tolerated agents that can be used in humans for digestive imaging studies. This MRI contrast should be useful for visualizing the anatomy of the digestive tract and particularly to differentiate between normal and pathological states, such as tumors. The solution has been proposed as zeolites or smectites (hectorite and montmorillonite) enclosing of paramagnetic metal ions obtained by ion-exchange methods. However, such materials could have problems of leakage of paramagnetic ions causing the appearance of the number side-effects. We propose the usage of the pillaring method for paramagnetic metal encapsulation in bentonites. By that way, paramagnetic cations like Fe(+3), Mn(+2) and Gd(+3) are introduced between clay mineral layers as polyoxo cations. After calcination, these polyoxo cations grow to be pillars (oxides of these metals) which are incorporated into the clay mineral matrix which prevents ion-leaching and dangerous side-effects. In this study we show that paramagnetic-pillared bentonites could be successfully used as MRI digestive tract non-leaching contrast agents, altering the longitudinal relaxation times of fluids in contact with the clay minerals.",
publisher = "Elsevier",
journal = "Applied Clay Science",
title = "Paramagnetic pillared bentonites - The new digestive tract MRI contrast agents",
volume = "48",
number = "1-2",
pages = "191-194",
doi = "10.1016/j.clay.2009.11.041"
}

Mojović, M., Dakovic, M., Banković, P.,& Mojović, Z.. (2010). Paramagnetic pillared bentonites - The new digestive tract MRI contrast agents. in Applied Clay Science
Elsevier., 48(1-2), 191-194.
https://doi.org/10.1016/j.clay.2009.11.041

Mojović M, Dakovic M, Banković P, Mojović Z. Paramagnetic pillared bentonites - The new digestive tract MRI contrast agents. in Applied Clay Science. 2010;48(1-2):191-194.
doi:10.1016/j.clay.2009.11.041 .

Mojović, Miloš, Dakovic, Marko, Banković, Predrag, Mojović, Zorica, "Paramagnetic pillared bentonites - The new digestive tract MRI contrast agents" in Applied Clay Science, 48, no. 1-2 (2010):191-194,
https://doi.org/10.1016/j.clay.2009.11.041 . .

TY  - CONF
AU  - Banković, Predrag
AU  - Milutinović Nikolić, Aleksandra
AU  - Jović-Jovičić, Nataša
AU  - Žunić, Marija
AU  - Vuković, Zorica
AU  - Abu-Rabi Stanković, Anđela
PY  - 2010
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/6636
AB  - In this work a series of Al,Fe-pillared clays (PILCs) with different Fe3+ content was synthesized and characterized. Their catalytic performance was studied in the in catalytic wet peroxide oxidation (CWPO) of food dye tartrazine used as a model compound. Degree of decolorization of tartrazine containing aqueous solution was monitored in relation to Fe3+ content. The results of the catalytic tests showed that higher Fe content leads to higher catalyst efficiency in the investigated reaction. The reaction can be described by 0-order kinetics inherent to heterogeneous catalytic processes.
PB  - Society of Physical Chemists of Serbia
C3  - Proceedings - X International Conference on fundamental and applied aspects of Physical chemistry, 21-24 September 2010, Belgrade
T1  - The influence of Fe content in Al,Fe-pillared clays on its performance in catalytic wet oxidation
VL  - I
SP  - 107
EP  - 109
UR  - https://hdl.handle.net/21.15107/rcub_cer_6636
ER  - 

@conference{
author = "Banković, Predrag and Milutinović Nikolić, Aleksandra and Jović-Jovičić, Nataša and Žunić, Marija and Vuković, Zorica and Abu-Rabi Stanković, Anđela",
year = "2010",
abstract = "In this work a series of Al,Fe-pillared clays (PILCs) with different Fe3+ content was synthesized and characterized. Their catalytic performance was studied in the in catalytic wet peroxide oxidation (CWPO) of food dye tartrazine used as a model compound. Degree of decolorization of tartrazine containing aqueous solution was monitored in relation to Fe3+ content. The results of the catalytic tests showed that higher Fe content leads to higher catalyst efficiency in the investigated reaction. The reaction can be described by 0-order kinetics inherent to heterogeneous catalytic processes.",
publisher = "Society of Physical Chemists of Serbia",
journal = "Proceedings - X International Conference on fundamental and applied aspects of Physical chemistry, 21-24 September 2010, Belgrade",
title = "The influence of Fe content in Al,Fe-pillared clays on its performance in catalytic wet oxidation",
volume = "I",
pages = "107-109",
url = "https://hdl.handle.net/21.15107/rcub_cer_6636"
}

Banković, P., Milutinović Nikolić, A., Jović-Jovičić, N., Žunić, M., Vuković, Z.,& Abu-Rabi Stanković, A.. (2010). The influence of Fe content in Al,Fe-pillared clays on its performance in catalytic wet oxidation. in Proceedings - X International Conference on fundamental and applied aspects of Physical chemistry, 21-24 September 2010, Belgrade
Society of Physical Chemists of Serbia., I, 107-109.
https://hdl.handle.net/21.15107/rcub_cer_6636

Banković P, Milutinović Nikolić A, Jović-Jovičić N, Žunić M, Vuković Z, Abu-Rabi Stanković A. The influence of Fe content in Al,Fe-pillared clays on its performance in catalytic wet oxidation. in Proceedings - X International Conference on fundamental and applied aspects of Physical chemistry, 21-24 September 2010, Belgrade. 2010;I:107-109.
https://hdl.handle.net/21.15107/rcub_cer_6636 .

Banković, Predrag, Milutinović Nikolić, Aleksandra, Jović-Jovičić, Nataša, Žunić, Marija, Vuković, Zorica, Abu-Rabi Stanković, Anđela, "The influence of Fe content in Al,Fe-pillared clays on its performance in catalytic wet oxidation" in Proceedings - X International Conference on fundamental and applied aspects of Physical chemistry, 21-24 September 2010, Belgrade, I (2010):107-109,
https://hdl.handle.net/21.15107/rcub_cer_6636 .

TY  - CONF
AU  - Mojović, Zorica
AU  - Banković, Predrag
AU  - Jović-Jovičić, Nataša
AU  - Žunić, Marija
AU  - Abu Rabi-Stanković, Anđela
AU  - Marinović, Sanja
PY  - 2010
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/6320
AB  - Zeolite NaX was modified by Pt and Pt/Ru nanodispersed metallic clusters. This
modification was achieved by zeolite impregnation with acetylacetonate salt/acetone
solution, followed by acetone evaporation and thermal decomposition of
organometallic complex. The mixture of modified zeolite and 10 wt.% of carbon black,
in a form of thin layer, was pasted to a glassy carbon surface by nafion. Electrocatalytic
properties of metal-modified zeolites were tested in methanol electrooxidation reaction.
PB  - Society of Physical Chemists of Serbia
C3  - Proceedings - 10th International Conference on Fundamental and Applied Aspects of Physical Chemistry, Physical Chemistry 2010, 21-24 September 2010, Belgrade, Serbia
T1  - Methanol electrooxidation from alkaline solution on pt and PtRu modified Zeolite X
SP  - 286
EP  - 288
UR  - https://hdl.handle.net/21.15107/rcub_cer_6320
ER  - 

@conference{
author = "Mojović, Zorica and Banković, Predrag and Jović-Jovičić, Nataša and Žunić, Marija and Abu Rabi-Stanković, Anđela and Marinović, Sanja",
year = "2010",
abstract = "Zeolite NaX was modified by Pt and Pt/Ru nanodispersed metallic clusters. This
modification was achieved by zeolite impregnation with acetylacetonate salt/acetone
solution, followed by acetone evaporation and thermal decomposition of
organometallic complex. The mixture of modified zeolite and 10 wt.% of carbon black,
in a form of thin layer, was pasted to a glassy carbon surface by nafion. Electrocatalytic
properties of metal-modified zeolites were tested in methanol electrooxidation reaction.",
publisher = "Society of Physical Chemists of Serbia",
journal = "Proceedings - 10th International Conference on Fundamental and Applied Aspects of Physical Chemistry, Physical Chemistry 2010, 21-24 September 2010, Belgrade, Serbia",
title = "Methanol electrooxidation from alkaline solution on pt and PtRu modified Zeolite X",
pages = "286-288",
url = "https://hdl.handle.net/21.15107/rcub_cer_6320"
}

Mojović, Z., Banković, P., Jović-Jovičić, N., Žunić, M., Abu Rabi-Stanković, A.,& Marinović, S.. (2010). Methanol electrooxidation from alkaline solution on pt and PtRu modified Zeolite X. in Proceedings - 10th International Conference on Fundamental and Applied Aspects of Physical Chemistry, Physical Chemistry 2010, 21-24 September 2010, Belgrade, Serbia
Society of Physical Chemists of Serbia., 286-288.
https://hdl.handle.net/21.15107/rcub_cer_6320

Mojović Z, Banković P, Jović-Jovičić N, Žunić M, Abu Rabi-Stanković A, Marinović S. Methanol electrooxidation from alkaline solution on pt and PtRu modified Zeolite X. in Proceedings - 10th International Conference on Fundamental and Applied Aspects of Physical Chemistry, Physical Chemistry 2010, 21-24 September 2010, Belgrade, Serbia. 2010;:286-288.
https://hdl.handle.net/21.15107/rcub_cer_6320 .

Mojović, Zorica, Banković, Predrag, Jović-Jovičić, Nataša, Žunić, Marija, Abu Rabi-Stanković, Anđela, Marinović, Sanja, "Methanol electrooxidation from alkaline solution on pt and PtRu modified Zeolite X" in Proceedings - 10th International Conference on Fundamental and Applied Aspects of Physical Chemistry, Physical Chemistry 2010, 21-24 September 2010, Belgrade, Serbia (2010):286-288,
https://hdl.handle.net/21.15107/rcub_cer_6320 .

TY  - JOUR
AU  - Mojović, Zorica
AU  - Milutinović Nikolić, Aleksandra
AU  - Banković, Predrag
AU  - Mentus, Slavko
AU  - Jovanović, Dušan M.
PY  - 2010
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/634
AB  - In order to enhance silver effectiveness for oxygen reduction reaction, pillared clay was used as a support for silver nanodispersion. Silver particles incorporation into pillared clay pores was attempted by impregnation/thermal degradation technique. X-ray diffraction as well as adsorption-desorption isotherms confirmed that pillaring procedure was successful. Scanning electron microscopy evidenced that a part of silver appeared outside the pillared clay cavities. Ag-pillared clay composite homogenized with 10 wt.% of nanodispersed carbon black (Vulcan), was applied on a flat glassy carbon surface and used as an electrode material. Oxygen reduction reaction was investigated in an O(2)-saturated aqueous 0.1 M NaOH solution.
PB  - Springer, New York
T2  - Journal of Solid State Electrochemistry
T1  - Electrochemical behavior of silver-impregnated Al-pillared smectite in alkaline solution
VL  - 14
IS  - 9
SP  - 1621
EP  - 1627
DO  - 10.1007/s10008-010-1006-z
ER  - 

@article{
author = "Mojović, Zorica and Milutinović Nikolić, Aleksandra and Banković, Predrag and Mentus, Slavko and Jovanović, Dušan M.",
year = "2010",
abstract = "In order to enhance silver effectiveness for oxygen reduction reaction, pillared clay was used as a support for silver nanodispersion. Silver particles incorporation into pillared clay pores was attempted by impregnation/thermal degradation technique. X-ray diffraction as well as adsorption-desorption isotherms confirmed that pillaring procedure was successful. Scanning electron microscopy evidenced that a part of silver appeared outside the pillared clay cavities. Ag-pillared clay composite homogenized with 10 wt.% of nanodispersed carbon black (Vulcan), was applied on a flat glassy carbon surface and used as an electrode material. Oxygen reduction reaction was investigated in an O(2)-saturated aqueous 0.1 M NaOH solution.",
publisher = "Springer, New York",
journal = "Journal of Solid State Electrochemistry",
title = "Electrochemical behavior of silver-impregnated Al-pillared smectite in alkaline solution",
volume = "14",
number = "9",
pages = "1621-1627",
doi = "10.1007/s10008-010-1006-z"
}

Mojović, Z., Milutinović Nikolić, A., Banković, P., Mentus, S.,& Jovanović, D. M.. (2010). Electrochemical behavior of silver-impregnated Al-pillared smectite in alkaline solution. in Journal of Solid State Electrochemistry
Springer, New York., 14(9), 1621-1627.
https://doi.org/10.1007/s10008-010-1006-z

Mojović Z, Milutinović Nikolić A, Banković P, Mentus S, Jovanović DM. Electrochemical behavior of silver-impregnated Al-pillared smectite in alkaline solution. in Journal of Solid State Electrochemistry. 2010;14(9):1621-1627.
doi:10.1007/s10008-010-1006-z .

Mojović, Zorica, Milutinović Nikolić, Aleksandra, Banković, Predrag, Mentus, Slavko, Jovanović, Dušan M., "Electrochemical behavior of silver-impregnated Al-pillared smectite in alkaline solution" in Journal of Solid State Electrochemistry, 14, no. 9 (2010):1621-1627,
https://doi.org/10.1007/s10008-010-1006-z . .

TY  - JOUR
AU  - Mojović, Zorica
AU  - Banković, Predrag
AU  - Milutinović Nikolić, Aleksandra
AU  - Nedic, B.
AU  - Jovanović, Dušan M.
PY  - 2010
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/651
AB  - The influence of aluminosilicate support on the catalyst efficiency was investigated. Three different aluminosilicate materials containing cobalt (II) ion as active specie for phenol or nitrite oxidation were obtained. The first sample was zeolite 13X impregnated with Co by impregnation/thermal degradation procedure using Co-acetylacetonate. Bentonite was pillared with Al(3+)/Co(2+) mixture to obtain the second sample. For the third one Co was introduced into Al-pillared bentonite by ion-exchange using Co(NO(3))(2)*6H(2)O. Reactions of either phenol or nitrite oxidation were used as test reactions for the investigation of the influence of the type of aluminosilicate support on the catalytic activity of Co.
PB  - Elsevier
T2  - Applied Clay Science
T1  - Co-aluminosilicate based electrodes
VL  - 48
IS  - 1-2
SP  - 179
EP  - 184
DO  - 10.1016/j.clay.2009.11.022
ER  - 

@article{
author = "Mojović, Zorica and Banković, Predrag and Milutinović Nikolić, Aleksandra and Nedic, B. and Jovanović, Dušan M.",
year = "2010",
abstract = "The influence of aluminosilicate support on the catalyst efficiency was investigated. Three different aluminosilicate materials containing cobalt (II) ion as active specie for phenol or nitrite oxidation were obtained. The first sample was zeolite 13X impregnated with Co by impregnation/thermal degradation procedure using Co-acetylacetonate. Bentonite was pillared with Al(3+)/Co(2+) mixture to obtain the second sample. For the third one Co was introduced into Al-pillared bentonite by ion-exchange using Co(NO(3))(2)*6H(2)O. Reactions of either phenol or nitrite oxidation were used as test reactions for the investigation of the influence of the type of aluminosilicate support on the catalytic activity of Co.",
publisher = "Elsevier",
journal = "Applied Clay Science",
title = "Co-aluminosilicate based electrodes",
volume = "48",
number = "1-2",
pages = "179-184",
doi = "10.1016/j.clay.2009.11.022"
}

Mojović, Z., Banković, P., Milutinović Nikolić, A., Nedic, B.,& Jovanović, D. M.. (2010). Co-aluminosilicate based electrodes. in Applied Clay Science
Elsevier., 48(1-2), 179-184.
https://doi.org/10.1016/j.clay.2009.11.022

Mojović Z, Banković P, Milutinović Nikolić A, Nedic B, Jovanović DM. Co-aluminosilicate based electrodes. in Applied Clay Science. 2010;48(1-2):179-184.
doi:10.1016/j.clay.2009.11.022 .

Mojović, Zorica, Banković, Predrag, Milutinović Nikolić, Aleksandra, Nedic, B., Jovanović, Dušan M., "Co-aluminosilicate based electrodes" in Applied Clay Science, 48, no. 1-2 (2010):179-184,
https://doi.org/10.1016/j.clay.2009.11.022 . .

TY  - JOUR
AU  - Jović-Jovičić, Nataša
AU  - Milutinović Nikolić, Aleksandra
AU  - Banković, Predrag
AU  - Mojović, Zorica
AU  - Žunić, Marija
AU  - Gržetić, Ivan
AU  - Jovanović, Dušan M.
PY  - 2010
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/740
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.
PB  - Elsevier
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 = "Jović-Jovičić, Nataša and Milutinović Nikolić, Aleksandra and Banković, Predrag and Mojović, Zorica and Žunić, Marija and Gržetić, Ivan and Jovanović, Dušan M.",
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.",
publisher = "Elsevier",
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"
}

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

Jović-Jovičić N, Milutinović Nikolić A, Banković P, Mojović Z, Žunić M, Gržetić I, Jovanović DM. 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 .

Jović-Jovičić, Nataša, Milutinović Nikolić, Aleksandra, Banković, Predrag, Mojović, Zorica, Žunić, Marija, Gržetić, Ivan, Jovanović, Dušan M., "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  - Banković, Predrag
AU  - Mojović, Zorica
AU  - Milutinović Nikolić, Aleksandra
AU  - Jović-Jovičić, Nataša
AU  - Marinović, Sanja
AU  - Jovanović, Dušan M.
PY  - 2010
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/637
AB  - Bentonite was pillared with Al, Al-Cu, Al-Fe or Al-Co poly(hydroxo metal) cations for electrochemical oxidation of phenol in acidic solution. Multisweep cyclic voltammetry was applied to analyze the behavior of the bentonite modified glassy carbon electrode. The influence of pillaring on the electrocatalytic properties was investigated. Reactivation of the electrodes after prolonged phenol oxidation was performed by cathodisation at -2 V.
PB  - Elsevier
T2  - Applied Clay Science
T1  - Mixed pillared bentonite for electrooxidation of phenol
VL  - 49
IS  - 1-2
SP  - 84
EP  - 89
DO  - 10.1016/j.clay.2010.04.012
ER  - 

@article{
author = "Banković, Predrag and Mojović, Zorica and Milutinović Nikolić, Aleksandra and Jović-Jovičić, Nataša and Marinović, Sanja and Jovanović, Dušan M.",
year = "2010",
abstract = "Bentonite was pillared with Al, Al-Cu, Al-Fe or Al-Co poly(hydroxo metal) cations for electrochemical oxidation of phenol in acidic solution. Multisweep cyclic voltammetry was applied to analyze the behavior of the bentonite modified glassy carbon electrode. The influence of pillaring on the electrocatalytic properties was investigated. Reactivation of the electrodes after prolonged phenol oxidation was performed by cathodisation at -2 V.",
publisher = "Elsevier",
journal = "Applied Clay Science",
title = "Mixed pillared bentonite for electrooxidation of phenol",
volume = "49",
number = "1-2",
pages = "84-89",
doi = "10.1016/j.clay.2010.04.012"
}

Banković, P., Mojović, Z., Milutinović Nikolić, A., Jović-Jovičić, N., Marinović, S.,& Jovanović, D. M.. (2010). Mixed pillared bentonite for electrooxidation of phenol. in Applied Clay Science
Elsevier., 49(1-2), 84-89.
https://doi.org/10.1016/j.clay.2010.04.012

Banković P, Mojović Z, Milutinović Nikolić A, Jović-Jovičić N, Marinović S, Jovanović DM. Mixed pillared bentonite for electrooxidation of phenol. in Applied Clay Science. 2010;49(1-2):84-89.
doi:10.1016/j.clay.2010.04.012 .

Banković, Predrag, Mojović, Zorica, Milutinović Nikolić, Aleksandra, Jović-Jovičić, Nataša, Marinović, Sanja, Jovanović, Dušan M., "Mixed pillared bentonite for electrooxidation of phenol" in Applied Clay Science, 49, no. 1-2 (2010):84-89,
https://doi.org/10.1016/j.clay.2010.04.012 . .

TY  - JOUR
AU  - Lukić, Ivana
AU  - Krstić, Jugoslav
AU  - Glisic, Sandra
AU  - Jovanović, Dušan M.
AU  - Skala, Dejan
PY  - 2010
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/640
AB  - In this study, catalysts for fatty acid methyl esters (FAME or biodiesel) synthesis with K2CO3 as the active component on an alumina/silica support were synthesized using the sol-gel method, which was followed by drying the 'dense' wet gels with supercritical carbon dioxide to obtain the aerogels. The prepared catalysts were characterized by XRD analysis, FTIR spectroscopy and N2 physisorption at 77 K, and tested in the methanolysis of sunflower oil. The effects of reaction variables, such as reaction time, temperature and methanol to oil molar ratio, on the yield of FAME were investigated. The aerogel catalysts with K2CO3 as the active component on an alumina/silica support exhibited good activity in the methanolysis of sunflower oil. The leaching of potassium when the catalyst was in contact with pure methanol under the working conditions of methanolysis was also tested in this study, indicating that it occurred only at higher temperatures, while at lower ones, it was negligible.
AB  - U ovom radu katalizator za sintezu metil estara masnih kiselina (MEMK ili biodizel) sa K2CO3 kao aktivnom komponentom na alumosilikatnom nosaču sintetizovan je sol-gel metodom nakon čega je dobijeni gel sušen uz prisustvo natkritičnog ugljen dioksida da bi se dobio aerogel. Za karakterizaciju sintetizovanih katalizatora korišćene su metode XRD, FTIR i N2 fizisorpcija na 77 K i katalizatori su testirani u reakciji metanolize suncokretovog ulja. Katalizator je testiran u reakciji metanolize suncekrotovog ulja i sintezi MEMK. Ispitan je uticaj različitih parametara kao što su vreme, temperatura i molarni odnos metanol : ulje na prinos MEMK. Aerogel katalizator sa K2CO3 kao aktivnom komponentom na alumosilikatnom nosaču pokazao je dobru katalitičku aktivnost u reakciji metanolize suncokretovog ulja. Izluživanje kalijuma u kontaktu sa metanolom na radnim uslovima metanolize takođe je testirano u ovom radu, pokazujući da ono postoji na višim temperaturama, dok je na nižim zanemarljivo.
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Biodiesel synthesis using K2CO3/Al-O-Si aerogel catalysts
T1  - Sinteza biodizela katalizovana alumosilikatnim aerogelom sa K2Co3
VL  - 75
IS  - 6
SP  - 789
EP  - 801
DO  - 10.2298/JSC090707047L
ER  - 

@article{
author = "Lukić, Ivana and Krstić, Jugoslav and Glisic, Sandra and Jovanović, Dušan M. and Skala, Dejan",
year = "2010",
abstract = "In this study, catalysts for fatty acid methyl esters (FAME or biodiesel) synthesis with K2CO3 as the active component on an alumina/silica support were synthesized using the sol-gel method, which was followed by drying the 'dense' wet gels with supercritical carbon dioxide to obtain the aerogels. The prepared catalysts were characterized by XRD analysis, FTIR spectroscopy and N2 physisorption at 77 K, and tested in the methanolysis of sunflower oil. The effects of reaction variables, such as reaction time, temperature and methanol to oil molar ratio, on the yield of FAME were investigated. The aerogel catalysts with K2CO3 as the active component on an alumina/silica support exhibited good activity in the methanolysis of sunflower oil. The leaching of potassium when the catalyst was in contact with pure methanol under the working conditions of methanolysis was also tested in this study, indicating that it occurred only at higher temperatures, while at lower ones, it was negligible., U ovom radu katalizator za sintezu metil estara masnih kiselina (MEMK ili biodizel) sa K2CO3 kao aktivnom komponentom na alumosilikatnom nosaču sintetizovan je sol-gel metodom nakon čega je dobijeni gel sušen uz prisustvo natkritičnog ugljen dioksida da bi se dobio aerogel. Za karakterizaciju sintetizovanih katalizatora korišćene su metode XRD, FTIR i N2 fizisorpcija na 77 K i katalizatori su testirani u reakciji metanolize suncokretovog ulja. Katalizator je testiran u reakciji metanolize suncekrotovog ulja i sintezi MEMK. Ispitan je uticaj različitih parametara kao što su vreme, temperatura i molarni odnos metanol : ulje na prinos MEMK. Aerogel katalizator sa K2CO3 kao aktivnom komponentom na alumosilikatnom nosaču pokazao je dobru katalitičku aktivnost u reakciji metanolize suncokretovog ulja. Izluživanje kalijuma u kontaktu sa metanolom na radnim uslovima metanolize takođe je testirano u ovom radu, pokazujući da ono postoji na višim temperaturama, dok je na nižim zanemarljivo.",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Biodiesel synthesis using K2CO3/Al-O-Si aerogel catalysts, Sinteza biodizela katalizovana alumosilikatnim aerogelom sa K2Co3",
volume = "75",
number = "6",
pages = "789-801",
doi = "10.2298/JSC090707047L"
}

Lukić, I., Krstić, J., Glisic, S., Jovanović, D. M.,& Skala, D.. (2010). Biodiesel synthesis using K2CO3/Al-O-Si aerogel catalysts. in Journal of the Serbian Chemical Society
Serbian Chemical Society., 75(6), 789-801.
https://doi.org/10.2298/JSC090707047L

Lukić I, Krstić J, Glisic S, Jovanović DM, Skala D. Biodiesel synthesis using K2CO3/Al-O-Si aerogel catalysts. in Journal of the Serbian Chemical Society. 2010;75(6):789-801.
doi:10.2298/JSC090707047L .

Lukić, Ivana, Krstić, Jugoslav, Glisic, Sandra, Jovanović, Dušan M., Skala, Dejan, "Biodiesel synthesis using K2CO3/Al-O-Si aerogel catalysts" in Journal of the Serbian Chemical Society, 75, no. 6 (2010):789-801,
https://doi.org/10.2298/JSC090707047L . .

TY  - CONF
AU  - Marinović, Vedrana
AU  - Marinović, Sanja
AU  - Jovanović, Mića
AU  - Jovanović, Jovan
AU  - Štrbac, Svetlana
PY  - 2010
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4181
AB  - Electrochemical reduction of trinitrololuene (TNT) based on the ready reduction of lheir electron-defficient nitro-groups was investigated using platinum electrode in aqueous sodium chloride solutions with acetonitrile containing different concentrations of TNT.
PB  - Nice : International Society of Electrochemistry
C3  - The 61st Annual Meeting of the International Society of Electrochemistry: Electrochemistry from Biology to Physics September 26th - October 1st, 2010, Nice, France: Book of Abstracts
T1  - Electrochemical Reduction of Trinitrotoluene on a Modified Platinum Electrode
SP  - s10-P-047
UR  - https://hdl.handle.net/21.15107/rcub_dais_3509
ER  - 

@conference{
author = "Marinović, Vedrana and Marinović, Sanja and Jovanović, Mića and Jovanović, Jovan and Štrbac, Svetlana",
year = "2010",
abstract = "Electrochemical reduction of trinitrololuene (TNT) based on the ready reduction of lheir electron-defficient nitro-groups was investigated using platinum electrode in aqueous sodium chloride solutions with acetonitrile containing different concentrations of TNT.",
publisher = "Nice : International Society of Electrochemistry",
journal = "The 61st Annual Meeting of the International Society of Electrochemistry: Electrochemistry from Biology to Physics September 26th - October 1st, 2010, Nice, France: Book of Abstracts",
title = "Electrochemical Reduction of Trinitrotoluene on a Modified Platinum Electrode",
pages = "s10-P-047",
url = "https://hdl.handle.net/21.15107/rcub_dais_3509"
}

Marinović, V., Marinović, S., Jovanović, M., Jovanović, J.,& Štrbac, S.. (2010). Electrochemical Reduction of Trinitrotoluene on a Modified Platinum Electrode. in The 61st Annual Meeting of the International Society of Electrochemistry: Electrochemistry from Biology to Physics September 26th - October 1st, 2010, Nice, France: Book of Abstracts
Nice : International Society of Electrochemistry., s10-P-047.
https://hdl.handle.net/21.15107/rcub_dais_3509

Marinović V, Marinović S, Jovanović M, Jovanović J, Štrbac S. Electrochemical Reduction of Trinitrotoluene on a Modified Platinum Electrode. in The 61st Annual Meeting of the International Society of Electrochemistry: Electrochemistry from Biology to Physics September 26th - October 1st, 2010, Nice, France: Book of Abstracts. 2010;:s10-P-047.
https://hdl.handle.net/21.15107/rcub_dais_3509 .

Marinović, Vedrana, Marinović, Sanja, Jovanović, Mića, Jovanović, Jovan, Štrbac, Svetlana, "Electrochemical Reduction of Trinitrotoluene on a Modified Platinum Electrode" in The 61st Annual Meeting of the International Society of Electrochemistry: Electrochemistry from Biology to Physics September 26th - October 1st, 2010, Nice, France: Book of Abstracts (2010):s10-P-047,
https://hdl.handle.net/21.15107/rcub_dais_3509 .

TY  - CONF
AU  - Štrbac, Svetlana
AU  - Marinović, Vedrana
AU  - Marinović, Sanja
AU  - Jovanović, Mića
AU  - Jovanović, Jovan
PY  - 2010
UR  - http://dais.sanu.ac.rs/123456789/243
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2848
AB  - Poster presented at the 61st Annual Meeting of the International Society of Electrochemistry, Nice, France, September 26 – October 1, 2010
T1  - Electrochemical Reduction of Trinitrotoluene on a Modified Platinum Electrode
UR  - https://hdl.handle.net/21.15107/rcub_dais_3509
ER  - 

@conference{
author = "Štrbac, Svetlana and Marinović, Vedrana and Marinović, Sanja and Jovanović, Mića and Jovanović, Jovan",
year = "2010",
abstract = "Poster presented at the 61st Annual Meeting of the International Society of Electrochemistry, Nice, France, September 26 – October 1, 2010",
title = "Electrochemical Reduction of Trinitrotoluene on a Modified Platinum Electrode",
url = "https://hdl.handle.net/21.15107/rcub_dais_3509"
}

Štrbac, S., Marinović, V., Marinović, S., Jovanović, M.,& Jovanović, J.. (2010). Electrochemical Reduction of Trinitrotoluene on a Modified Platinum Electrode. .
https://hdl.handle.net/21.15107/rcub_dais_3509

Štrbac S, Marinović V, Marinović S, Jovanović M, Jovanović J. Electrochemical Reduction of Trinitrotoluene on a Modified Platinum Electrode. 2010;.
https://hdl.handle.net/21.15107/rcub_dais_3509 .

Štrbac, Svetlana, Marinović, Vedrana, Marinović, Sanja, Jovanović, Mića, Jovanović, Jovan, "Electrochemical Reduction of Trinitrotoluene on a Modified Platinum Electrode" (2010),
https://hdl.handle.net/21.15107/rcub_dais_3509 .

TY  - JOUR
AU  - Marinović, Sanja
AU  - Popović, Ivanka G.
AU  - Dunjic, B.
AU  - Tasic, S.
AU  - Bozic, B.
AU  - Jovanović, Dušan M.
PY  - 2010
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/635
AB  - The aim of this study was to investigate the influence of different components of interpenetrating polymer networks (IPNs) on their behavior in dual curing automotive applications. Dual curing is one of possible ways to obtain fast curing, scratch resistant coatings for use in OEM and car refinish applications. Dual curing systems, upon hardening, represent interpenetrating networks (IPNs) [1]. IPN's were obtained using novel acrylate-terminated hyperbranched polyester with high functionality and compared to classical 2-pack polyurethane clear coat. In our previous manuscript [1] we investigated the influence of the acrylated hyperbranched polyester (HBP(A)) content in dual curing systems. In this article we studied the influence of the reactive diluent on dual curing compositions. To this end, we have chosen IPN with 50/50 weigth ratio of polyurethane (PU) and polyacrylic (PA) component. In order to determine more clearly the role of the HBP(A) in one IPN HBP(A) was changed with hexane diol diacrylate (HDDA), keeping the same ratio with EHA. The IPNs were characterized by dynamic-mechanical analysis (DMA), differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). The mechanical properties of the IPNs were also investigated. The IPN with HDDA as reactive diluent, had the best performance. IPN with H BP(A) had the highest glass transition temperature Tg and the highest crosslink density, but it did not have the highest hardness.
PB  - Elsevier Science Sa, Lausanne
T2  - Progress in Organic Coatings
T1  - The influence of different components on interpenetrating polymer network's (IPN's) characteristics as automotive top coats
VL  - 68
IS  - 4
SP  - 293
EP  - 298
DO  - 10.1016/j.porgcoat.2010.03.010
ER  - 

@article{
author = "Marinović, Sanja and Popović, Ivanka G. and Dunjic, B. and Tasic, S. and Bozic, B. and Jovanović, Dušan M.",
year = "2010",
abstract = "The aim of this study was to investigate the influence of different components of interpenetrating polymer networks (IPNs) on their behavior in dual curing automotive applications. Dual curing is one of possible ways to obtain fast curing, scratch resistant coatings for use in OEM and car refinish applications. Dual curing systems, upon hardening, represent interpenetrating networks (IPNs) [1]. IPN's were obtained using novel acrylate-terminated hyperbranched polyester with high functionality and compared to classical 2-pack polyurethane clear coat. In our previous manuscript [1] we investigated the influence of the acrylated hyperbranched polyester (HBP(A)) content in dual curing systems. In this article we studied the influence of the reactive diluent on dual curing compositions. To this end, we have chosen IPN with 50/50 weigth ratio of polyurethane (PU) and polyacrylic (PA) component. In order to determine more clearly the role of the HBP(A) in one IPN HBP(A) was changed with hexane diol diacrylate (HDDA), keeping the same ratio with EHA. The IPNs were characterized by dynamic-mechanical analysis (DMA), differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). The mechanical properties of the IPNs were also investigated. The IPN with HDDA as reactive diluent, had the best performance. IPN with H BP(A) had the highest glass transition temperature Tg and the highest crosslink density, but it did not have the highest hardness.",
publisher = "Elsevier Science Sa, Lausanne",
journal = "Progress in Organic Coatings",
title = "The influence of different components on interpenetrating polymer network's (IPN's) characteristics as automotive top coats",
volume = "68",
number = "4",
pages = "293-298",
doi = "10.1016/j.porgcoat.2010.03.010"
}

Marinović, S., Popović, I. G., Dunjic, B., Tasic, S., Bozic, B.,& Jovanović, D. M.. (2010). The influence of different components on interpenetrating polymer network's (IPN's) characteristics as automotive top coats. in Progress in Organic Coatings
Elsevier Science Sa, Lausanne., 68(4), 293-298.
https://doi.org/10.1016/j.porgcoat.2010.03.010

Marinović S, Popović IG, Dunjic B, Tasic S, Bozic B, Jovanović DM. The influence of different components on interpenetrating polymer network's (IPN's) characteristics as automotive top coats. in Progress in Organic Coatings. 2010;68(4):293-298.
doi:10.1016/j.porgcoat.2010.03.010 .

Marinović, Sanja, Popović, Ivanka G., Dunjic, B., Tasic, S., Bozic, B., Jovanović, Dušan M., "The influence of different components on interpenetrating polymer network's (IPN's) characteristics as automotive top coats" in Progress in Organic Coatings, 68, no. 4 (2010):293-298,
https://doi.org/10.1016/j.porgcoat.2010.03.010 . .

TY  - JOUR
AU  - Lončarević, Davor
AU  - Krstić, Jugoslav
AU  - Dostanić, Jasmina
AU  - Manojlović, Dragan
AU  - Čupić, Željko
AU  - Jovanović, Dušan M.
PY  - 2010
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/744
AB  - Polymer supported catalysts with Co(II) and Cr(VI) ions were prepared and characterized by means of FTIR, diffuse reflectance UV-vis, nitrogen physisorption, mercury porosimetry and SEM-EDX measurements. The catalytic activity and selectivity of the polymer supported catalysts were tested in aerobic liquid-phase partial oxidation of cyclohexane in a polytetrafluoroethylene lined reactor. The influence of reaction time and temperature, main products addition, mass of the catalyst and different metals loading was investigated. Product yield and cyclohexyl hydroperoxide formation in the catalytic system were used as critical parameters which could be optimized by changing the cobalt content on the polymer and the catalyst mass used in the catalytic runs. By increasing cobalt content, a higher activity and corresponding lower selectivity towards cyclohexanone were obtained. This study indicates that the selectivity towards cyclohexanone and cyclohexanol is mainly defined by the yield and type of the catalyst with minor influence of temperature and main products addition. In addition catalysts were used for deperoxidation of cyclohexyl hydroperoxide in mild conditions. Nearly the same selectivity towards cyclohexanone and cyclohexanol is achieved using the cobalt containing catalyst, while a higher selectivity towards cyclohexanone is achieved using the chromium containing catalysts.
PB  - Elsevier Science Sa, Lausanne
T2  - Chemical Engineering Journal
T1  - Cyclohexane oxidation and cyclohexyl hydroperoxide decomposition by poly(4-vinylpyridine-co-divinylbenzene) supported cobalt and chromium complexes
VL  - 157
IS  - 1
SP  - 181
EP  - 188
DO  - 10.1016/j.cej.2009.11.034
ER  - 

@article{
author = "Lončarević, Davor and Krstić, Jugoslav and Dostanić, Jasmina and Manojlović, Dragan and Čupić, Željko and Jovanović, Dušan M.",
year = "2010",
abstract = "Polymer supported catalysts with Co(II) and Cr(VI) ions were prepared and characterized by means of FTIR, diffuse reflectance UV-vis, nitrogen physisorption, mercury porosimetry and SEM-EDX measurements. The catalytic activity and selectivity of the polymer supported catalysts were tested in aerobic liquid-phase partial oxidation of cyclohexane in a polytetrafluoroethylene lined reactor. The influence of reaction time and temperature, main products addition, mass of the catalyst and different metals loading was investigated. Product yield and cyclohexyl hydroperoxide formation in the catalytic system were used as critical parameters which could be optimized by changing the cobalt content on the polymer and the catalyst mass used in the catalytic runs. By increasing cobalt content, a higher activity and corresponding lower selectivity towards cyclohexanone were obtained. This study indicates that the selectivity towards cyclohexanone and cyclohexanol is mainly defined by the yield and type of the catalyst with minor influence of temperature and main products addition. In addition catalysts were used for deperoxidation of cyclohexyl hydroperoxide in mild conditions. Nearly the same selectivity towards cyclohexanone and cyclohexanol is achieved using the cobalt containing catalyst, while a higher selectivity towards cyclohexanone is achieved using the chromium containing catalysts.",
publisher = "Elsevier Science Sa, Lausanne",
journal = "Chemical Engineering Journal",
title = "Cyclohexane oxidation and cyclohexyl hydroperoxide decomposition by poly(4-vinylpyridine-co-divinylbenzene) supported cobalt and chromium complexes",
volume = "157",
number = "1",
pages = "181-188",
doi = "10.1016/j.cej.2009.11.034"
}

Lončarević, D., Krstić, J., Dostanić, J., Manojlović, D., Čupić, Ž.,& Jovanović, D. M.. (2010). Cyclohexane oxidation and cyclohexyl hydroperoxide decomposition by poly(4-vinylpyridine-co-divinylbenzene) supported cobalt and chromium complexes. in Chemical Engineering Journal
Elsevier Science Sa, Lausanne., 157(1), 181-188.
https://doi.org/10.1016/j.cej.2009.11.034

Lončarević D, Krstić J, Dostanić J, Manojlović D, Čupić Ž, Jovanović DM. Cyclohexane oxidation and cyclohexyl hydroperoxide decomposition by poly(4-vinylpyridine-co-divinylbenzene) supported cobalt and chromium complexes. in Chemical Engineering Journal. 2010;157(1):181-188.
doi:10.1016/j.cej.2009.11.034 .

Lončarević, Davor, Krstić, Jugoslav, Dostanić, Jasmina, Manojlović, Dragan, Čupić, Željko, Jovanović, Dušan M., "Cyclohexane oxidation and cyclohexyl hydroperoxide decomposition by poly(4-vinylpyridine-co-divinylbenzene) supported cobalt and chromium complexes" in Chemical Engineering Journal, 157, no. 1 (2010):181-188,
https://doi.org/10.1016/j.cej.2009.11.034 . .

TY  - JOUR
AU  - Marinović, Vedrana M.
AU  - Marinović, Sanja
AU  - Jovanović, M.
AU  - Jovanovic, J.
AU  - Štrbac, Svetlana
PY  - 2010
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/720
AB  - The electrochemical reduction of 2,4,6-trinitrotoluene (TNT) was investigated by cyclic voltammetry on a platinum electrode in aqueous sodium chloride solutions with acetonitrile containing different concentrations of TNT. The obtained cyclic voltammograms showed three distinct reduction peaks in the potential range of -0.45 to -0.8 V (vs. an Ag/AgCl (3M KCl) reference electrode), which refer to the multi-step process of TNT reduction. The calibration curves of the dependence of the first peak current on the TNT concentration were linear in the ranges 4.4-638.4 mu M and 0.11-4.40 mu M for two different scan rates, 200 my s(-1) and 20 mV s(-1), respectively. The detection limit was 0.11 mu M. Acetonitrile chemisorption on Pt surface took place and caused thus modified platinum electrode to exhibit an electrochemically stabile behaviour. Hence, a very high reproducibility over a prolonged time and voltammetric cycling was provided for using a Pt wire that is easy to handle as a suitable material for TNT sensing. Additionally, it was confirmed by testing the acetonitrile modified Pt wire for TNT detection in river water.
PB  - Elsevier
T2  - Journal of Electroanalytical Chemistry
T1  - The electrochemical reduction of trinitrotoluene on a platinum wire modified by chemisorbed acetonitrile
VL  - 648
IS  - 1
SP  - 1
EP  - 7
DO  - 10.1016/j.jelechem.2010.07.008
ER  - 

@article{
author = "Marinović, Vedrana M. and Marinović, Sanja and Jovanović, M. and Jovanovic, J. and Štrbac, Svetlana",
year = "2010",
abstract = "The electrochemical reduction of 2,4,6-trinitrotoluene (TNT) was investigated by cyclic voltammetry on a platinum electrode in aqueous sodium chloride solutions with acetonitrile containing different concentrations of TNT. The obtained cyclic voltammograms showed three distinct reduction peaks in the potential range of -0.45 to -0.8 V (vs. an Ag/AgCl (3M KCl) reference electrode), which refer to the multi-step process of TNT reduction. The calibration curves of the dependence of the first peak current on the TNT concentration were linear in the ranges 4.4-638.4 mu M and 0.11-4.40 mu M for two different scan rates, 200 my s(-1) and 20 mV s(-1), respectively. The detection limit was 0.11 mu M. Acetonitrile chemisorption on Pt surface took place and caused thus modified platinum electrode to exhibit an electrochemically stabile behaviour. Hence, a very high reproducibility over a prolonged time and voltammetric cycling was provided for using a Pt wire that is easy to handle as a suitable material for TNT sensing. Additionally, it was confirmed by testing the acetonitrile modified Pt wire for TNT detection in river water.",
publisher = "Elsevier",
journal = "Journal of Electroanalytical Chemistry",
title = "The electrochemical reduction of trinitrotoluene on a platinum wire modified by chemisorbed acetonitrile",
volume = "648",
number = "1",
pages = "1-7",
doi = "10.1016/j.jelechem.2010.07.008"
}

Marinović, V. M., Marinović, S., Jovanović, M., Jovanovic, J.,& Štrbac, S.. (2010). The electrochemical reduction of trinitrotoluene on a platinum wire modified by chemisorbed acetonitrile. in Journal of Electroanalytical Chemistry
Elsevier., 648(1), 1-7.
https://doi.org/10.1016/j.jelechem.2010.07.008

Marinović VM, Marinović S, Jovanović M, Jovanovic J, Štrbac S. The electrochemical reduction of trinitrotoluene on a platinum wire modified by chemisorbed acetonitrile. in Journal of Electroanalytical Chemistry. 2010;648(1):1-7.
doi:10.1016/j.jelechem.2010.07.008 .

Marinović, Vedrana M., Marinović, Sanja, Jovanović, M., Jovanovic, J., Štrbac, Svetlana, "The electrochemical reduction of trinitrotoluene on a platinum wire modified by chemisorbed acetonitrile" in Journal of Electroanalytical Chemistry, 648, no. 1 (2010):1-7,
https://doi.org/10.1016/j.jelechem.2010.07.008 . .

TY  - JOUR
AU  - Jović-Jovičić, Nataša
AU  - Milutinović Nikolić, Aleksandra
AU  - Banković, Predrag
AU  - Dojčinović, Biljana
AU  - Nedić, B.
AU  - Gržetić, Ivan
AU  - Jovanović, Dušan M.
PY  - 2010
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/627
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 A
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 = "Jović-Jovičić, Nataša and Milutinović Nikolić, Aleksandra and Banković, Predrag and Dojčinović, Biljana and Nedić, B. and Gržetić, Ivan and Jovanović, Dušan M.",
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 A",
title = "Synthesis, Characterization and Adsorptive Properties of Organobentonites",
volume = "117",
number = "5",
pages = "849-854",
doi = "10.12693/APhysPolA.117.849"
}

Jović-Jovičić, N., Milutinović Nikolić, A., Banković, P., Dojčinović, B., Nedić, B., Gržetić, I.,& Jovanović, D. M.. (2010). Synthesis, Characterization and Adsorptive Properties of Organobentonites. in Acta Physica Polonica A
Polish Acad Sciences Inst Physics, Warsaw., 117(5), 849-854.
https://doi.org/10.12693/APhysPolA.117.849

Jović-Jovičić N, Milutinović Nikolić A, Banković P, Dojčinović B, Nedić B, Gržetić I, Jovanović DM. Synthesis, Characterization and Adsorptive Properties of Organobentonites. in Acta Physica Polonica A. 2010;117(5):849-854.
doi:10.12693/APhysPolA.117.849 .

Jović-Jovičić, Nataša, Milutinović Nikolić, Aleksandra, Banković, Predrag, Dojčinović, Biljana, Nedić, B., Gržetić, Ivan, Jovanović, Dušan M., "Synthesis, Characterization and Adsorptive Properties of Organobentonites" in Acta Physica Polonica A, 117, no. 5 (2010):849-854,
https://doi.org/10.12693/APhysPolA.117.849 . .

TY  - JOUR
AU  - Žunić, Marija
AU  - Milutinović Nikolić, Aleksandra
AU  - Jović-Jovičić, Nataša
AU  - Banković, Predrag
AU  - Mojović, Zorica
AU  - Manojlović, Dragan
AU  - Jovanović, Dušan M.
PY  - 2010
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/723
AB  - Modification and characterization of bentonite from location Bogovina, Serbia was performed in order to obtain material applicable in wastewater purification. The  LT 75μm bentonite fraction was used in organobentonite synthesis while the  LT 2μm 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°C. The (001) smectite peak around 2θ = 6° shifts during the modification process. The Na-exchange process lowered d001 from 1.53 nm (2θ = 5.78°) for starting clay to 1.28 nm (2θ = 6.92°), 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 d001 to 2.00 nm for organobentonite. Specific surface area, SBET, was affected by particle size and type of modification. The samples with finer bentonite fraction had higher SBET due to increased smectite content. Na-exchanged bentonite samples had higher SBET value than starting clay samples of same granulation. Organo modification caused dramatic decrease in SBET value, while the pillaring process lead to an increase of SBET 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 SBET. 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 = "Žunić, Marija and Milutinović Nikolić, Aleksandra and Jović-Jovičić, Nataša and Banković, Predrag and Mojović, Zorica and Manojlović, Dragan 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 75μm bentonite fraction was used in organobentonite synthesis while the  LT 2μm 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°C. The (001) smectite peak around 2θ = 6° shifts during the modification process. The Na-exchange process lowered d001 from 1.53 nm (2θ = 5.78°) for starting clay to 1.28 nm (2θ = 6.92°), 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 d001 to 2.00 nm for organobentonite. Specific surface area, SBET, was affected by particle size and type of modification. The samples with finer bentonite fraction had higher SBET due to increased smectite content. Na-exchanged bentonite samples had higher SBET value than starting clay samples of same granulation. Organo modification caused dramatic decrease in SBET value, while the pillaring process lead to an increase of SBET 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 SBET. 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"
}

Žunić, M., Milutinović Nikolić, A., Jović-Jovičić, N., Banković, P., Mojović, Z., Manojlović, 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

Žunić M, Milutinović Nikolić A, Jović-Jovičić N, Banković P, Mojović Z, Manojlović D, 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 .

Žunić, Marija, Milutinović Nikolić, Aleksandra, Jović-Jovičić, Nataša, Banković, Predrag, Mojović, Zorica, Manojlović, Dragan, 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  - CONF
AU  - Žunić, Marija
AU  - Milutinović Nikolić, Aleksandra
AU  - Jović-Jovičić, Nataša
AU  - Banković, Predrag
AU  - Mojović, Zorica
AU  - Manojlović, Dragan
AU  - Jovanović, Dušan
PY  - 2009
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/6988
AB  - Izvršena je modifikacija i karakterizacija bentonita s ciljem dobijanja nanomaterijala primenljivog u prečišćavanju 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.
PB  - Institut tehničkih nauka Srpske akademije nauka i umetnosti
C3  - Program i knjiga apstrakata - VIII konferencija mladih istraživača - Nauka i inženjerstvo materijala
T1  - Modifikovani bentonit kao sorbent i katalizator za prečišćavanje otpadih voda koje sadrže boje
SP  - 25
EP  - 25
UR  - https://hdl.handle.net/21.15107/rcub_cer_6988
ER  - 

@conference{
author = "Žunić, Marija and Milutinović Nikolić, Aleksandra and Jović-Jovičić, Nataša and Banković, Predrag and Mojović, Zorica and Manojlović, Dragan and Jovanović, Dušan",
year = "2009",
abstract = "Izvršena je modifikacija i karakterizacija bentonita s ciljem dobijanja nanomaterijala primenljivog u prečišćavanju 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.",
publisher = "Institut tehničkih nauka Srpske akademije nauka i umetnosti",
journal = "Program i knjiga apstrakata - VIII konferencija mladih istraživača - Nauka i inženjerstvo materijala",
title = "Modifikovani bentonit kao sorbent i katalizator za prečišćavanje otpadih voda koje sadrže boje",
pages = "25-25",
url = "https://hdl.handle.net/21.15107/rcub_cer_6988"
}

Žunić, M., Milutinović Nikolić, A., Jović-Jovičić, N., Banković, P., Mojović, Z., Manojlović, D.,& Jovanović, D.. (2009). Modifikovani bentonit kao sorbent i katalizator za prečišćavanje otpadih voda koje sadrže boje. in Program i knjiga apstrakata - VIII konferencija mladih istraživača - Nauka i inženjerstvo materijala
Institut tehničkih nauka Srpske akademije nauka i umetnosti., 25-25.
https://hdl.handle.net/21.15107/rcub_cer_6988

Žunić M, Milutinović Nikolić A, Jović-Jovičić N, Banković P, Mojović Z, Manojlović D, Jovanović D. Modifikovani bentonit kao sorbent i katalizator za prečišćavanje otpadih voda koje sadrže boje. in Program i knjiga apstrakata - VIII konferencija mladih istraživača - Nauka i inženjerstvo materijala. 2009;:25-25.
https://hdl.handle.net/21.15107/rcub_cer_6988 .

Žunić, Marija, Milutinović Nikolić, Aleksandra, Jović-Jovičić, Nataša, Banković, Predrag, Mojović, Zorica, Manojlović, Dragan, Jovanović, Dušan, "Modifikovani bentonit kao sorbent i katalizator za prečišćavanje otpadih voda koje sadrže boje" in Program i knjiga apstrakata - VIII konferencija mladih istraživača - Nauka i inženjerstvo materijala (2009):25-25,
https://hdl.handle.net/21.15107/rcub_cer_6988 .

TY  - JOUR
AU  - Mojović, Zorica
AU  - Milutinović Nikolić, Aleksandra
AU  - Mentus, Slavko
AU  - Jovanović, Dušan M.
PY  - 2009
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/531
AB  - Nanodispersed metallic clusters of platinum, silver and cobalt were incorporated into NaX zeolite cavities by impregnation with acetone solution of corresponding acetylacetonates and solvent evaporation followed by acetylacetonate thermal decomposition. The mixture of modified zeolites and 10 wt % of carbon black, in the form of a thin layer, was pasted onto a glassy carbon surface by Nafion. With such electrode materials, the phenol oxidation in neutral, alkaline and acid solution was studied by cyclovoltammetry. Deactivation of A electrodes in both neutral and alkaline medium was observed, indicating that polymerization reaction might be the main reaction pathway of phenol at higher pH values. Formation of quinine-type structures was obtained during electro-oxidation at lower pH values, being more significant in acidic solutions.
PB  - Wiley-V C H Verlag Gmbh, Weinheim
T2  - Chemical Engineering & Technology
T1  - Electrochemical Oxidation of Phenol on Metal-Impregnated Zeolite Electrodes
VL  - 32
IS  - 5
SP  - 738
EP  - 744
DO  - 10.1002/ceat.200800546
ER  - 

@article{
author = "Mojović, Zorica and Milutinović Nikolić, Aleksandra and Mentus, Slavko and Jovanović, Dušan M.",
year = "2009",
abstract = "Nanodispersed metallic clusters of platinum, silver and cobalt were incorporated into NaX zeolite cavities by impregnation with acetone solution of corresponding acetylacetonates and solvent evaporation followed by acetylacetonate thermal decomposition. The mixture of modified zeolites and 10 wt % of carbon black, in the form of a thin layer, was pasted onto a glassy carbon surface by Nafion. With such electrode materials, the phenol oxidation in neutral, alkaline and acid solution was studied by cyclovoltammetry. Deactivation of A electrodes in both neutral and alkaline medium was observed, indicating that polymerization reaction might be the main reaction pathway of phenol at higher pH values. Formation of quinine-type structures was obtained during electro-oxidation at lower pH values, being more significant in acidic solutions.",
publisher = "Wiley-V C H Verlag Gmbh, Weinheim",
journal = "Chemical Engineering & Technology",
title = "Electrochemical Oxidation of Phenol on Metal-Impregnated Zeolite Electrodes",
volume = "32",
number = "5",
pages = "738-744",
doi = "10.1002/ceat.200800546"
}

Mojović, Z., Milutinović Nikolić, A., Mentus, S.,& Jovanović, D. M.. (2009). Electrochemical Oxidation of Phenol on Metal-Impregnated Zeolite Electrodes. in Chemical Engineering & Technology
Wiley-V C H Verlag Gmbh, Weinheim., 32(5), 738-744.
https://doi.org/10.1002/ceat.200800546

Mojović Z, Milutinović Nikolić A, Mentus S, Jovanović DM. Electrochemical Oxidation of Phenol on Metal-Impregnated Zeolite Electrodes. in Chemical Engineering & Technology. 2009;32(5):738-744.
doi:10.1002/ceat.200800546 .

Mojović, Zorica, Milutinović Nikolić, Aleksandra, Mentus, Slavko, Jovanović, Dušan M., "Electrochemical Oxidation of Phenol on Metal-Impregnated Zeolite Electrodes" in Chemical Engineering & Technology, 32, no. 5 (2009):738-744,
https://doi.org/10.1002/ceat.200800546 . .