Vasiljević-Nedić, Bojana

Link to this page

Authority KeyName Variants
orcid::0000-0003-1967-3937
  • Vasiljević-Nedić, Bojana (4)

Author's Bibliography

The quest for optimal water quantity in the synthesis of metal-organic framework MOF-5

Savić-Biserčić, Marjetka; Marjanović, Budimir; Vasiljević-Nedić, Bojana; Mentus, Slavko V.; Zasonska, Beata A.; Ćirić-Marjanović, Gordana N.

(2019)

TY  - JOUR
AU  - Savić-Biserčić, Marjetka
AU  - Marjanović, Budimir
AU  - Vasiljević-Nedić, Bojana
AU  - Mentus, Slavko V.
AU  - Zasonska, Beata A.
AU  - Ćirić-Marjanović, Gordana N.
PY  - 2019
UR  - https://linkinghub.elsevier.com/retrieve/pii/S1387181118305766
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7969
AB  - Efficient and simple room temperature synthesis of pure phase metal-organic framework MOF-5 has been developed, based on the use of anhydrous zinc acetate, Zn(OAc)2, as a precursor, instead of zinc acetate dihydrate. Crucial influence of water on a reaction pathway was revealed. In order to obtain MOF-5, different amounts of water have been added into the solutions of Zn(OAc)2 in N,N-dimethylformamide (DMF) to prepare in situ zinc acetate hydrates with 0.25, 0.5, and 1.0 mol of water. Commercially available zinc acetate dihydrate was also used as a precursor for comparison. These solutions were mixed at room temperature with the solution of 1,4-benzenedicarboxylic acid in DMF in the absence of any base. Based on XRD, FTIR, and SEM measurements, it was shown that the optimal amount of water for the synthesis of completely pure, crystalline phase MOF-5 is 0.25–0.5 mol of water per one mole of Zn. The reaction systems with 1.0 and 2.0 mol of water per one mole of Zn also led to solids with MOF-5 as the dominant phase, but they also contain small amounts of another phase, formed due to the decomposition (hydrolysis) and/or distortion of the MOF-5 framework in the presence of excess amounts of water. The product synthesized in the system without any added water contains MOF-5 phase in a very small amount, while main phase is zinc 1,4-benzenedicarboxylate and/or zinc hydrogen 1,4-benzenedicarboxylate. Regular cubic submicro/microcrystal morphology exhibited the samples synthesized using 0.5 and 0.25 mol water per one mole of Zn (pure MOF-5), while for the samples synthesized at mole ratios H2O/Zn2+ = 1.0 and 2.0 other particle shapes are also seen. By nitrogen sorption measurements it was found that the highest values of BET specific surface area (1937 m2 g−1), micropore volume (0.83 cm3 g−1), and micropore area (1590 m2 g−1) showed MOF-5 prepared at mole ratio H2O/Zn2+ = 0.5, while the highest yield of MOF-5 is obtained with the theoretical mole ratio H2O/Zn2+ = 0.25. Thermal stability of synthesized materials was investigated by TGA. © 2018 Elsevier Inc.
T2  - Microporous and Mesoporous Materials
T1  - The quest for optimal water quantity in the synthesis of metal-organic framework MOF-5
VL  - 278
SP  - 23
EP  - 29
DO  - 10.1016/j.micromeso.2018.11.005
ER  - 
@article{
author = "Savić-Biserčić, Marjetka and Marjanović, Budimir and Vasiljević-Nedić, Bojana and Mentus, Slavko V. and Zasonska, Beata A. and Ćirić-Marjanović, Gordana N.",
year = "2019",
abstract = "Efficient and simple room temperature synthesis of pure phase metal-organic framework MOF-5 has been developed, based on the use of anhydrous zinc acetate, Zn(OAc)2, as a precursor, instead of zinc acetate dihydrate. Crucial influence of water on a reaction pathway was revealed. In order to obtain MOF-5, different amounts of water have been added into the solutions of Zn(OAc)2 in N,N-dimethylformamide (DMF) to prepare in situ zinc acetate hydrates with 0.25, 0.5, and 1.0 mol of water. Commercially available zinc acetate dihydrate was also used as a precursor for comparison. These solutions were mixed at room temperature with the solution of 1,4-benzenedicarboxylic acid in DMF in the absence of any base. Based on XRD, FTIR, and SEM measurements, it was shown that the optimal amount of water for the synthesis of completely pure, crystalline phase MOF-5 is 0.25–0.5 mol of water per one mole of Zn. The reaction systems with 1.0 and 2.0 mol of water per one mole of Zn also led to solids with MOF-5 as the dominant phase, but they also contain small amounts of another phase, formed due to the decomposition (hydrolysis) and/or distortion of the MOF-5 framework in the presence of excess amounts of water. The product synthesized in the system without any added water contains MOF-5 phase in a very small amount, while main phase is zinc 1,4-benzenedicarboxylate and/or zinc hydrogen 1,4-benzenedicarboxylate. Regular cubic submicro/microcrystal morphology exhibited the samples synthesized using 0.5 and 0.25 mol water per one mole of Zn (pure MOF-5), while for the samples synthesized at mole ratios H2O/Zn2+ = 1.0 and 2.0 other particle shapes are also seen. By nitrogen sorption measurements it was found that the highest values of BET specific surface area (1937 m2 g−1), micropore volume (0.83 cm3 g−1), and micropore area (1590 m2 g−1) showed MOF-5 prepared at mole ratio H2O/Zn2+ = 0.5, while the highest yield of MOF-5 is obtained with the theoretical mole ratio H2O/Zn2+ = 0.25. Thermal stability of synthesized materials was investigated by TGA. © 2018 Elsevier Inc.",
journal = "Microporous and Mesoporous Materials",
title = "The quest for optimal water quantity in the synthesis of metal-organic framework MOF-5",
volume = "278",
pages = "23-29",
doi = "10.1016/j.micromeso.2018.11.005"
}
Savić-Biserčić, M., Marjanović, B., Vasiljević-Nedić, B., Mentus, S. V., Zasonska, B. A.,& Ćirić-Marjanović, G. N.. (2019). The quest for optimal water quantity in the synthesis of metal-organic framework MOF-5. in Microporous and Mesoporous Materials, 278, 23-29.
https://doi.org/10.1016/j.micromeso.2018.11.005
Savić-Biserčić M, Marjanović B, Vasiljević-Nedić B, Mentus SV, Zasonska BA, Ćirić-Marjanović GN. The quest for optimal water quantity in the synthesis of metal-organic framework MOF-5. in Microporous and Mesoporous Materials. 2019;278:23-29.
doi:10.1016/j.micromeso.2018.11.005 .
Savić-Biserčić, Marjetka, Marjanović, Budimir, Vasiljević-Nedić, Bojana, Mentus, Slavko V., Zasonska, Beata A., Ćirić-Marjanović, Gordana N., "The quest for optimal water quantity in the synthesis of metal-organic framework MOF-5" in Microporous and Mesoporous Materials, 278 (2019):23-29,
https://doi.org/10.1016/j.micromeso.2018.11.005 . .
1
38
20
36

In situ synthesis of potassium tungstophosphate supported on BEA zeolite and perspective application for pesticide removal

Vasiljević-Nedić, Bojana; Obradović, Milena; Bajuk-Bogdanović, Danica V.; Milojević-Rakić, Maja; Jovanović, Zoran M.; Gavrilov, Nemanja M.; Holclajtner-Antunović, Ivanka D.

(2019)

TY  - JOUR
AU  - Vasiljević-Nedić, Bojana
AU  - Obradović, Milena
AU  - Bajuk-Bogdanović, Danica V.
AU  - Milojević-Rakić, Maja
AU  - Jovanović, Zoran M.
AU  - Gavrilov, Nemanja M.
AU  - Holclajtner-Antunović, Ivanka D.
PY  - 2019
UR  - https://linkinghub.elsevier.com/retrieve/pii/S1001074218314682
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8217
AB  - Potassium tungstophosphate is supported on BEA zeolite by in situ synthesis for glyphosate removal. Spectroscopic measurements identified hydrogen bonding as a primal interaction of potassium salt and BEA zeolite. Composites are evaluated for glyphosate herbicide removal and adsorption process is analyzed using two isotherm models. Obtained adsorption capacities for all prepared composites lay between 45.2 and 92.2 mg of glyphosate per gram of investigated composite. Suspension acidity revealed that glyphosate is adsorbed mainly in the zwitter-ion form at the composite surface while the amount of potassium salt in the composites is crucial for the adsorption application. Exceptional adsorption behavior is postulated to come from a high degree of homogeneity among surface active sites which is confirmed by different experimental methods. Temperature programmed desorption of glyphosate coupled with mass spectrometer detected one broad, high-temperature peak which represents overlapped desorption processes from active sights of similar strength. Introduction of potassium tungstophosphate affects active sites present in BEA zeolite for glyphosate desorption and significantly increases the amount of adsorbed pesticide in comparison to BEA zeolite. Supporting of potassium tungstophosphate on BEA zeolite via in situ synthesis procedure enables the formation of highly efficient adsorbents and revealed their perspective environmental application. © 2019
T2  - Journal of Environmental Sciences
T1  - In situ synthesis of potassium tungstophosphate supported on BEA zeolite and perspective application for pesticide removal
VL  - 81
SP  - 136
EP  - 147
DO  - 10.1016/j.jes.2019.01.018
ER  - 
@article{
author = "Vasiljević-Nedić, Bojana and Obradović, Milena and Bajuk-Bogdanović, Danica V. and Milojević-Rakić, Maja and Jovanović, Zoran M. and Gavrilov, Nemanja M. and Holclajtner-Antunović, Ivanka D.",
year = "2019",
abstract = "Potassium tungstophosphate is supported on BEA zeolite by in situ synthesis for glyphosate removal. Spectroscopic measurements identified hydrogen bonding as a primal interaction of potassium salt and BEA zeolite. Composites are evaluated for glyphosate herbicide removal and adsorption process is analyzed using two isotherm models. Obtained adsorption capacities for all prepared composites lay between 45.2 and 92.2 mg of glyphosate per gram of investigated composite. Suspension acidity revealed that glyphosate is adsorbed mainly in the zwitter-ion form at the composite surface while the amount of potassium salt in the composites is crucial for the adsorption application. Exceptional adsorption behavior is postulated to come from a high degree of homogeneity among surface active sites which is confirmed by different experimental methods. Temperature programmed desorption of glyphosate coupled with mass spectrometer detected one broad, high-temperature peak which represents overlapped desorption processes from active sights of similar strength. Introduction of potassium tungstophosphate affects active sites present in BEA zeolite for glyphosate desorption and significantly increases the amount of adsorbed pesticide in comparison to BEA zeolite. Supporting of potassium tungstophosphate on BEA zeolite via in situ synthesis procedure enables the formation of highly efficient adsorbents and revealed their perspective environmental application. © 2019",
journal = "Journal of Environmental Sciences",
title = "In situ synthesis of potassium tungstophosphate supported on BEA zeolite and perspective application for pesticide removal",
volume = "81",
pages = "136-147",
doi = "10.1016/j.jes.2019.01.018"
}
Vasiljević-Nedić, B., Obradović, M., Bajuk-Bogdanović, D. V., Milojević-Rakić, M., Jovanović, Z. M., Gavrilov, N. M.,& Holclajtner-Antunović, I. D.. (2019). In situ synthesis of potassium tungstophosphate supported on BEA zeolite and perspective application for pesticide removal. in Journal of Environmental Sciences, 81, 136-147.
https://doi.org/10.1016/j.jes.2019.01.018
Vasiljević-Nedić B, Obradović M, Bajuk-Bogdanović DV, Milojević-Rakić M, Jovanović ZM, Gavrilov NM, Holclajtner-Antunović ID. In situ synthesis of potassium tungstophosphate supported on BEA zeolite and perspective application for pesticide removal. in Journal of Environmental Sciences. 2019;81:136-147.
doi:10.1016/j.jes.2019.01.018 .
Vasiljević-Nedić, Bojana, Obradović, Milena, Bajuk-Bogdanović, Danica V., Milojević-Rakić, Maja, Jovanović, Zoran M., Gavrilov, Nemanja M., Holclajtner-Antunović, Ivanka D., "In situ synthesis of potassium tungstophosphate supported on BEA zeolite and perspective application for pesticide removal" in Journal of Environmental Sciences, 81 (2019):136-147,
https://doi.org/10.1016/j.jes.2019.01.018 . .
17
9
17

Characterization and electrochemical properties of organomodified and corresponding derived carbonized clay

Jović-Jovičić, Nataša P.; Mojović, Miloš D.; Stanković, Dalibor M.; Vasiljević-Nedić, Bojana; Milutinović-Nikolić, Aleksandra D.; Banković, Predrag T.; Mojović, Zorica D.

(2019)

TY  - JOUR
AU  - Jović-Jovičić, Nataša P.
AU  - Mojović, Miloš D.
AU  - Stanković, Dalibor M.
AU  - Vasiljević-Nedić, Bojana
AU  - Milutinović-Nikolić, Aleksandra D.
AU  - Banković, Predrag T.
AU  - Mojović, Zorica D.
PY  - 2019
UR  - https://linkinghub.elsevier.com/retrieve/pii/S0013468618325039
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7979
AB  - Series of alkylammonium modified smectites with different alkylammoinum/clay ratios was synthesized (H series). The obtained organoclays were used as precursors for carbon-clay composite materials (C series). Both set of materials were characterized by X-ray diffraction (XRD), point of zero charge (pHPZC), N2 adsorption-desorption isotherms, Raman spectroscopy and electron paramagnetic resonance (EPR) analysis. XRD analysis of organomodified clays confirmed incorporation of HDTMA+ into interlamellar space of smectite. Series of carbonized clays showed constant d001 value of 1.4 nm. The pHPZC of two series differed indicating that carbonization changed the profile of pH dependent sites on the clay surface. Textural properties of the H series decreased throughout the series, while in the C series the most developed porous structure was obtained for sample where HDTMA+ loading was equal to cation exchange capacity. Raman spectroscopy showed that amorphous carbon was formed during carbonization process. The obtained materials were used as modifiers of carbon paste electrode and investigated using electrochemical impedance spectroscopy, cyclic voltammetry and square wave voltammetry. The comparison of electrochemical behavior of H series and C series showed the importance of interlamellar species for charge transfer process. The investigation of influence of composition of carbon paste and form of added carbon showed that performance of carbon-clay based electrodes depended on synergy of different factors. © 2018 Elsevier Ltd
T2  - Electrochimica Acta
T1  - Characterization and electrochemical properties of organomodified and corresponding derived carbonized clay
VL  - 296
SP  - 387
EP  - 396
DO  - 10.1016/j.electacta.2018.11.031
ER  - 
@article{
author = "Jović-Jovičić, Nataša P. and Mojović, Miloš D. and Stanković, Dalibor M. and Vasiljević-Nedić, Bojana and Milutinović-Nikolić, Aleksandra D. and Banković, Predrag T. and Mojović, Zorica D.",
year = "2019",
abstract = "Series of alkylammonium modified smectites with different alkylammoinum/clay ratios was synthesized (H series). The obtained organoclays were used as precursors for carbon-clay composite materials (C series). Both set of materials were characterized by X-ray diffraction (XRD), point of zero charge (pHPZC), N2 adsorption-desorption isotherms, Raman spectroscopy and electron paramagnetic resonance (EPR) analysis. XRD analysis of organomodified clays confirmed incorporation of HDTMA+ into interlamellar space of smectite. Series of carbonized clays showed constant d001 value of 1.4 nm. The pHPZC of two series differed indicating that carbonization changed the profile of pH dependent sites on the clay surface. Textural properties of the H series decreased throughout the series, while in the C series the most developed porous structure was obtained for sample where HDTMA+ loading was equal to cation exchange capacity. Raman spectroscopy showed that amorphous carbon was formed during carbonization process. The obtained materials were used as modifiers of carbon paste electrode and investigated using electrochemical impedance spectroscopy, cyclic voltammetry and square wave voltammetry. The comparison of electrochemical behavior of H series and C series showed the importance of interlamellar species for charge transfer process. The investigation of influence of composition of carbon paste and form of added carbon showed that performance of carbon-clay based electrodes depended on synergy of different factors. © 2018 Elsevier Ltd",
journal = "Electrochimica Acta",
title = "Characterization and electrochemical properties of organomodified and corresponding derived carbonized clay",
volume = "296",
pages = "387-396",
doi = "10.1016/j.electacta.2018.11.031"
}
Jović-Jovičić, N. P., Mojović, M. D., Stanković, D. M., Vasiljević-Nedić, B., Milutinović-Nikolić, A. D., Banković, P. T.,& Mojović, Z. D.. (2019). Characterization and electrochemical properties of organomodified and corresponding derived carbonized clay. in Electrochimica Acta, 296, 387-396.
https://doi.org/10.1016/j.electacta.2018.11.031
Jović-Jovičić NP, Mojović MD, Stanković DM, Vasiljević-Nedić B, Milutinović-Nikolić AD, Banković PT, Mojović ZD. Characterization and electrochemical properties of organomodified and corresponding derived carbonized clay. in Electrochimica Acta. 2019;296:387-396.
doi:10.1016/j.electacta.2018.11.031 .
Jović-Jovičić, Nataša P., Mojović, Miloš D., Stanković, Dalibor M., Vasiljević-Nedić, Bojana, Milutinović-Nikolić, Aleksandra D., Banković, Predrag T., Mojović, Zorica D., "Characterization and electrochemical properties of organomodified and corresponding derived carbonized clay" in Electrochimica Acta, 296 (2019):387-396,
https://doi.org/10.1016/j.electacta.2018.11.031 . .
7
5
8

Transformation of Cs-exchanged clinoptilolite to CsAlSi5O12 by hot-pressing

Omerašević, Mia; Ružić, Jovana; Vasiljević-Nedić, Bojana; Baščarević, Zvezdana D.; Bučevac, Dušan; Orlić, Jovana; Matović, Ljiljana

(2017)

TY  - JOUR
AU  - Omerašević, Mia
AU  - Ružić, Jovana
AU  - Vasiljević-Nedić, Bojana
AU  - Baščarević, Zvezdana D.
AU  - Bučevac, Dušan
AU  - Orlić, Jovana
AU  - Matović, Ljiljana
PY  - 2017
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1734
AB  - Dense CsAlSi5O12 was successfully obtained by hot pressing of Cs-exchanged clinoptilolite at 900 degrees C. Simultaneous application of high temperature and mechanical pressure allowed formation of CsAlSi5O12 at temperature considerably lower than 1150 degrees C which was the lowest reported temperature of CsAlSi5O12 formation in pressureless sintered Cs-exchanged clinoptilolite. CsAlSi5O12 formation was preceded by complete amorphisation of Cs-exchanged clinoptilolite in temperature range between 700 and 900 degrees C. Bearing in mind that clinoptilolite possesses high affinity for Cs cation it is believed that hot pressing of Cs-exchanged clinoptilolite might be an efficient way to immobilize radioactive Cs by its incorporation into crystal lattice of stable CsAlSi5O12. The samples sintered at 950 degrees C had relative density about 84% of theoretical density and open porosity of only 6% which is expected to result in low Cs leaching rate.
T2  - Ceramics International
T1  - Transformation of Cs-exchanged clinoptilolite to CsAlSi5O12 by hot-pressing
VL  - 43
IS  - 16
SP  - 13500
EP  - 13504
DO  - 10.1016/j.ceramint.2017.07.055
ER  - 
@article{
author = "Omerašević, Mia and Ružić, Jovana and Vasiljević-Nedić, Bojana and Baščarević, Zvezdana D. and Bučevac, Dušan and Orlić, Jovana and Matović, Ljiljana",
year = "2017",
abstract = "Dense CsAlSi5O12 was successfully obtained by hot pressing of Cs-exchanged clinoptilolite at 900 degrees C. Simultaneous application of high temperature and mechanical pressure allowed formation of CsAlSi5O12 at temperature considerably lower than 1150 degrees C which was the lowest reported temperature of CsAlSi5O12 formation in pressureless sintered Cs-exchanged clinoptilolite. CsAlSi5O12 formation was preceded by complete amorphisation of Cs-exchanged clinoptilolite in temperature range between 700 and 900 degrees C. Bearing in mind that clinoptilolite possesses high affinity for Cs cation it is believed that hot pressing of Cs-exchanged clinoptilolite might be an efficient way to immobilize radioactive Cs by its incorporation into crystal lattice of stable CsAlSi5O12. The samples sintered at 950 degrees C had relative density about 84% of theoretical density and open porosity of only 6% which is expected to result in low Cs leaching rate.",
journal = "Ceramics International",
title = "Transformation of Cs-exchanged clinoptilolite to CsAlSi5O12 by hot-pressing",
volume = "43",
number = "16",
pages = "13500-13504",
doi = "10.1016/j.ceramint.2017.07.055"
}
Omerašević, M., Ružić, J., Vasiljević-Nedić, B., Baščarević, Z. D., Bučevac, D., Orlić, J.,& Matović, L.. (2017). Transformation of Cs-exchanged clinoptilolite to CsAlSi5O12 by hot-pressing. in Ceramics International, 43(16), 13500-13504.
https://doi.org/10.1016/j.ceramint.2017.07.055
Omerašević M, Ružić J, Vasiljević-Nedić B, Baščarević ZD, Bučevac D, Orlić J, Matović L. Transformation of Cs-exchanged clinoptilolite to CsAlSi5O12 by hot-pressing. in Ceramics International. 2017;43(16):13500-13504.
doi:10.1016/j.ceramint.2017.07.055 .
Omerašević, Mia, Ružić, Jovana, Vasiljević-Nedić, Bojana, Baščarević, Zvezdana D., Bučevac, Dušan, Orlić, Jovana, Matović, Ljiljana, "Transformation of Cs-exchanged clinoptilolite to CsAlSi5O12 by hot-pressing" in Ceramics International, 43, no. 16 (2017):13500-13504,
https://doi.org/10.1016/j.ceramint.2017.07.055 . .
10
5
8