Sinteza, karakterizacija i testiranje katalitičkih svojstava specijalno dizajniranih materijala

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Sinteza, karakterizacija i testiranje katalitičkih svojstava specijalno dizajniranih materijala (en)
Синтеза, карактеризација и тестирање каталитичких својстава специјално дизајнираних материјала (sr)
Sinteza, karakterizacija i testiranje katalitičkih svojstava specijalno dizajniranih materijala (sr_RS)
Authors

Publications

Modified Bentonite as Adsorbent and Catalyst for Purification of Wastewaters Containing Dyes

Zunic, Marija J.; Milutinović-Nikolić, Aleksandra D.; Jović-Jovičić, Nataša; Banković, Predrag; Mojović, Zorica D.; Manojlović, Dragan D.; Jovanović, Dušan M.

(Assoc Chemists & Chemical Engineers Of Serbia, Belgrade, 2010)

TY  - JOUR
AU  - Zunic, Marija J.
AU  - Milutinović-Nikolić, Aleksandra D.
AU  - Jović-Jovičić, Nataša
AU  - Banković, Predrag
AU  - Mojović, Zorica D.
AU  - Manojlović, Dragan D.
AU  - Jovanović, Dušan M.
PY  - 2010
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1093
AB  - Modification and characterization of bentonite from location Bogovina, Serbia was performed in order to obtain material applicable in wastewater purification. The  lt 75 mu m bentonite fraction was used in organobentonite synthesis while the  lt 2 mu m bentonite fraction, obtained by hydroseparation was used in pillaring procedure. Organo-modification of bentonite was performed with (1-hexadecyl)trimethylammonium bromide (HDTMA-Br). Pillared bentonite was obtained using standard procedure. Al3+ and Fe3+ were incorporated in pillars in 4:1 ratio and applied as catalyst in catalytic wet peroxide oxidation. Differences in structure of starting and modified bentonites were established by XRD analysis and nitrogen physisorption on -196 degrees C. The (001) smectite peak around 2 theta = 6 degrees shifts during the modification process. The Na-exchange process lowered d(001) from 1.53 nm (2 theta = 5.78 degrees) for starting clay to 1.28 nm (2 theta = 6.92 degrees), but the clay retained its swelling properties. The pillaring process increased and fixed the basal spacing to 1.74 nm. Intercalation of HDTMA ions into smectite structure increased d(001) to 2.00 nm for organobentonite. Specific surface area, S-BET, was affected by particle size and type of modification. The samples with finer bentonite fraction had higher S-BET due to increased smectite content. Na-exchanged bentonite samples had higher S-BET value than starting clay samples of same granulation. Organomodification caused dramatic decrease in S-BET value, while the pillaring process lead to an increase of S-BET value. Adsorptive and catalytic purification of wastewaters containing dyes was tested using Acid Yellow 99 as a model dye. Na-exchanged bentonite had greater adsorption affinity for dye adsorption than raw bentonite owing to higher S-BET. By organomodification this affinity was enhanced more than 70 times due to transition of bentonite surface from hydrophilic to organophilic. Al,Fe pillared bentonite was proven to be efficient in catalytic wet peroxide oxidation of Acid Yellow 99 dye at room temperature.
AB  - Izvršena je modifikacija i karakterizacija bentonita radi dobijanja materijala za prečišćavanje otpadnih voda. Organo-modifikacija bentonita izvedena je pomoću heksadeciltrimetilamonijum-bromida. Pilareni bentonit dobijen je standardnim postupkom uz ugradnju Al3+ i Fe3+ jona u odnosu 4:1, i korišćen je kao katalizator za oksidativnu razgradnju u prisustvu vodonik-peroksida. Razlike u strukturi polaznog i modifikovanih bentonita utvrđene su rendgeno-strukturnom analizom i fizisorpcijom azota na -196°C. Ispitivano je adsorpciono i katalitičko prečišćavanje otpadnih voda koje sadrže boje, korišćenjem Acid Yellow 99 kao model boje. Izvršeno je poređenje katalitičkih i adsorpiconih svojstava modifikovanih bentonita.
PB  - Assoc Chemists & Chemical Engineers Of Serbia, Belgrade
T2  - Hemijska industrija
T1  - Modified Bentonite as Adsorbent and Catalyst for Purification of Wastewaters Containing Dyes
T1  - Modifikovani bentonit kao adsorbent i katalizator za prečišćavanje otpadnih voda koje sadrže boje
VL  - 64
IS  - 3
SP  - 193
EP  - 199
DO  - 10.2298/HEMIND091221023Z
ER  - 
@article{
author = "Zunic, Marija J. and Milutinović-Nikolić, Aleksandra D. and Jović-Jovičić, Nataša and Banković, Predrag and Mojović, Zorica D. and Manojlović, Dragan D. and Jovanović, Dušan M.",
year = "2010",
abstract = "Modification and characterization of bentonite from location Bogovina, Serbia was performed in order to obtain material applicable in wastewater purification. The  lt 75 mu m bentonite fraction was used in organobentonite synthesis while the  lt 2 mu m bentonite fraction, obtained by hydroseparation was used in pillaring procedure. Organo-modification of bentonite was performed with (1-hexadecyl)trimethylammonium bromide (HDTMA-Br). Pillared bentonite was obtained using standard procedure. Al3+ and Fe3+ were incorporated in pillars in 4:1 ratio and applied as catalyst in catalytic wet peroxide oxidation. Differences in structure of starting and modified bentonites were established by XRD analysis and nitrogen physisorption on -196 degrees C. The (001) smectite peak around 2 theta = 6 degrees shifts during the modification process. The Na-exchange process lowered d(001) from 1.53 nm (2 theta = 5.78 degrees) for starting clay to 1.28 nm (2 theta = 6.92 degrees), but the clay retained its swelling properties. The pillaring process increased and fixed the basal spacing to 1.74 nm. Intercalation of HDTMA ions into smectite structure increased d(001) to 2.00 nm for organobentonite. Specific surface area, S-BET, was affected by particle size and type of modification. The samples with finer bentonite fraction had higher S-BET due to increased smectite content. Na-exchanged bentonite samples had higher S-BET value than starting clay samples of same granulation. Organomodification caused dramatic decrease in S-BET value, while the pillaring process lead to an increase of S-BET value. Adsorptive and catalytic purification of wastewaters containing dyes was tested using Acid Yellow 99 as a model dye. Na-exchanged bentonite had greater adsorption affinity for dye adsorption than raw bentonite owing to higher S-BET. By organomodification this affinity was enhanced more than 70 times due to transition of bentonite surface from hydrophilic to organophilic. Al,Fe pillared bentonite was proven to be efficient in catalytic wet peroxide oxidation of Acid Yellow 99 dye at room temperature., Izvršena je modifikacija i karakterizacija bentonita radi dobijanja materijala za prečišćavanje otpadnih voda. Organo-modifikacija bentonita izvedena je pomoću heksadeciltrimetilamonijum-bromida. Pilareni bentonit dobijen je standardnim postupkom uz ugradnju Al3+ i Fe3+ jona u odnosu 4:1, i korišćen je kao katalizator za oksidativnu razgradnju u prisustvu vodonik-peroksida. Razlike u strukturi polaznog i modifikovanih bentonita utvrđene su rendgeno-strukturnom analizom i fizisorpcijom azota na -196°C. Ispitivano je adsorpciono i katalitičko prečišćavanje otpadnih voda koje sadrže boje, korišćenjem Acid Yellow 99 kao model boje. Izvršeno je poređenje katalitičkih i adsorpiconih svojstava modifikovanih bentonita.",
publisher = "Assoc Chemists & Chemical Engineers Of Serbia, Belgrade",
journal = "Hemijska industrija",
title = "Modified Bentonite as Adsorbent and Catalyst for Purification of Wastewaters Containing Dyes, Modifikovani bentonit kao adsorbent i katalizator za prečišćavanje otpadnih voda koje sadrže boje",
volume = "64",
number = "3",
pages = "193-199",
doi = "10.2298/HEMIND091221023Z"
}
Zunic, M. J., Milutinović-Nikolić, A. D., Jović-Jovičić, N., Banković, P., Mojović, Z. D., Manojlović, D. D.,& Jovanović, D. M.. (2010). Modified Bentonite as Adsorbent and Catalyst for Purification of Wastewaters Containing Dyes. in Hemijska industrija
Assoc Chemists & Chemical Engineers Of Serbia, Belgrade., 64(3), 193-199.
https://doi.org/10.2298/HEMIND091221023Z
Zunic MJ, Milutinović-Nikolić AD, Jović-Jovičić N, Banković P, Mojović ZD, Manojlović DD, Jovanović DM. Modified Bentonite as Adsorbent and Catalyst for Purification of Wastewaters Containing Dyes. in Hemijska industrija. 2010;64(3):193-199.
doi:10.2298/HEMIND091221023Z .
Zunic, Marija J., Milutinović-Nikolić, Aleksandra D., Jović-Jovičić, Nataša, Banković, Predrag, Mojović, Zorica D., Manojlović, Dragan D., Jovanović, Dušan M., "Modified Bentonite as Adsorbent and Catalyst for Purification of Wastewaters Containing Dyes" in Hemijska industrija, 64, no. 3 (2010):193-199,
https://doi.org/10.2298/HEMIND091221023Z . .
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Synthesis, Characterization and Adsorptive Properties of Organobentonites

Jovic-Jovicic, N.; Milutinović-Nikolić, Aleksandra D.; Bankovic, P.; Dojčinović, Biljana P.; Nedic, B.; Gržetić, Ivan; Jovanovic, D.

(Polish Acad Sciences Inst Physics, Warsaw, 2010)

TY  - JOUR
AU  - Jovic-Jovicic, N.
AU  - Milutinović-Nikolić, Aleksandra D.
AU  - Bankovic, P.
AU  - Dojčinović, Biljana P.
AU  - Nedic, B.
AU  - Gržetić, Ivan
AU  - Jovanovic, D.
PY  - 2010
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1083
AB  - In this paper partial and complete substitution of cations in the interlayer region of clay with different amounts of two aliphatic ammonium cations was performed with aim of synthesis of organobentonites with multipurpose adsorption properties. Domestic clay from Bogovina was submitted according to a common procedure used for the obtention of organobentonite, which comprises the following steps: grinding, sieving, Na-exchange, cation exchange and drying. The samples were characterized by X-ray diffraction and infrared spectroscopy. The incorporation of surfactant molecules into smectite structure lead to constant increase of d(001) basal spacing. IR absorption bands assigned to methyl and methylene vibrations increased with the increase of surfactant/bentonite ratio and length of aliphatic chain in surfactant molecules. Adsorptive properties of the obtained materials were in accordance with their organophylicity: the adsorption of organic dye increased while the rate of removal of Pb2+ by adsorption decreased.
PB  - Polish Acad Sciences Inst Physics, Warsaw
T2  - Acta Physica Polonica. Series A: General Physics, Physics of Condensed Matter, Optics and Quantum El
T1  - Synthesis, Characterization and Adsorptive Properties of Organobentonites
VL  - 117
IS  - 5
SP  - 849
EP  - 854
DO  - 10.12693/APhysPolA.117.849
ER  - 
@article{
author = "Jovic-Jovicic, N. and Milutinović-Nikolić, Aleksandra D. and Bankovic, P. and Dojčinović, Biljana P. and Nedic, B. and Gržetić, Ivan and Jovanovic, D.",
year = "2010",
abstract = "In this paper partial and complete substitution of cations in the interlayer region of clay with different amounts of two aliphatic ammonium cations was performed with aim of synthesis of organobentonites with multipurpose adsorption properties. Domestic clay from Bogovina was submitted according to a common procedure used for the obtention of organobentonite, which comprises the following steps: grinding, sieving, Na-exchange, cation exchange and drying. The samples were characterized by X-ray diffraction and infrared spectroscopy. The incorporation of surfactant molecules into smectite structure lead to constant increase of d(001) basal spacing. IR absorption bands assigned to methyl and methylene vibrations increased with the increase of surfactant/bentonite ratio and length of aliphatic chain in surfactant molecules. Adsorptive properties of the obtained materials were in accordance with their organophylicity: the adsorption of organic dye increased while the rate of removal of Pb2+ by adsorption decreased.",
publisher = "Polish Acad Sciences Inst Physics, Warsaw",
journal = "Acta Physica Polonica. Series A: General Physics, Physics of Condensed Matter, Optics and Quantum El",
title = "Synthesis, Characterization and Adsorptive Properties of Organobentonites",
volume = "117",
number = "5",
pages = "849-854",
doi = "10.12693/APhysPolA.117.849"
}
Jovic-Jovicic, N., Milutinović-Nikolić, A. D., Bankovic, P., Dojčinović, B. P., Nedic, B., Gržetić, I.,& Jovanovic, D.. (2010). Synthesis, Characterization and Adsorptive Properties of Organobentonites. in Acta Physica Polonica. Series A: General Physics, Physics of Condensed Matter, Optics and Quantum El
Polish Acad Sciences Inst Physics, Warsaw., 117(5), 849-854.
https://doi.org/10.12693/APhysPolA.117.849
Jovic-Jovicic N, Milutinović-Nikolić AD, Bankovic P, Dojčinović BP, Nedic B, Gržetić I, Jovanovic D. Synthesis, Characterization and Adsorptive Properties of Organobentonites. in Acta Physica Polonica. Series A: General Physics, Physics of Condensed Matter, Optics and Quantum El. 2010;117(5):849-854.
doi:10.12693/APhysPolA.117.849 .
Jovic-Jovicic, N., Milutinović-Nikolić, Aleksandra D., Bankovic, P., Dojčinović, Biljana P., Nedic, B., Gržetić, Ivan, Jovanovic, D., "Synthesis, Characterization and Adsorptive Properties of Organobentonites" in Acta Physica Polonica. Series A: General Physics, Physics of Condensed Matter, Optics and Quantum El, 117, no. 5 (2010):849-854,
https://doi.org/10.12693/APhysPolA.117.849 . .
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Cyclohexane oxidation and cyclohexyl hydroperoxide decomposition by poly(4-vinylpyridine-co-divinylbenzene) supported cobalt and chromium complexes

Lončarević, Davor; Krstic, J.; Dostanić, Jasmina; Manojlović, Dragan D.; Cupic, Z.; Jovanović, Dušan M.

(Elsevier Science Sa, Lausanne, 2010)

TY  - JOUR
AU  - Lončarević, Davor
AU  - Krstic, J.
AU  - Dostanić, Jasmina
AU  - Manojlović, Dragan D.
AU  - Cupic, Z.
AU  - Jovanović, Dušan M.
PY  - 2010
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1047
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. (C) 2009 Elsevier B. V. All rights reserved.
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 Krstic, J. and Dostanić, Jasmina and Manojlović, Dragan D. and Cupic, Z. 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. (C) 2009 Elsevier B. V. All rights reserved.",
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., Krstic, J., Dostanić, J., Manojlović, D. D., Cupic, Z.,& 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, Krstic J, Dostanić J, Manojlović DD, Cupic Z, 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, Krstic, J., Dostanić, Jasmina, Manojlović, Dragan D., Cupic, Z., 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 . .
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