TY  - JOUR
AU  - Popadić, Daliborka
AU  - Krstić, Jugoslav
AU  - Janošević-Ležaić, Aleksandra
AU  - Popović, Maja
AU  - Milojević-Rakić, Maja
AU  - Ignjatović, Ljubiša
AU  - Bajuk-Bogdanović, Danica
AU  - Gavrilov, Nemanja
PY  - 2024
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/5405
AB  - Reuse and/or recycling of spent adsorbents is taking a central role in modern thinking and catalyzed carbonization is the way forward. Herein we explore the carbonization of adsorbed acetamiprid, in an inert atmosphere, as a way of recycling and producing nitrogen-rich carbon material for potential use in supercapacitors. Added value material and the reuse of the adsorbent were achieved by carbonization at 700 °C under argon. The formation of a nitrogen-doped carbon layer as an active material on the adsorbent, bonded through a C-Si linkage, has been conclusively verified through elemental composition quantification using XPS and EDX measurements. Two-stage catalytic decomposition and condensation of the adsorbed pesticide is followed by TGA and TPD-MS. Attained carbon-based materials give stable Faradaic capacitance with a slight dependency on the number of adsorbing cycles. Capacitance calculated with respect to the adlayer carbon material reaches values as high as 610 F g−1. Galvanostatic Charge/Discharge measurement confirmed the stability of explored materials with a slight increase in capacitance over 1000 cycles. The presented results envisage electroactive materials preparation from environmental pollutants, adding value to spent adsorbents.
PB  - Elsevier B.V.
T2  - Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy
T1  - Acetamiprid's degradation products and mechanism: Part II – Inert atmosphere and charge storage
VL  - 308
DO  - 10.1016/j.saa.2023.123772
ER  - 

@article{
author = "Popadić, Daliborka and Krstić, Jugoslav and Janošević-Ležaić, Aleksandra and Popović, Maja and Milojević-Rakić, Maja and Ignjatović, Ljubiša and Bajuk-Bogdanović, Danica and Gavrilov, Nemanja",
year = "2024",
abstract = "Reuse and/or recycling of spent adsorbents is taking a central role in modern thinking and catalyzed carbonization is the way forward. Herein we explore the carbonization of adsorbed acetamiprid, in an inert atmosphere, as a way of recycling and producing nitrogen-rich carbon material for potential use in supercapacitors. Added value material and the reuse of the adsorbent were achieved by carbonization at 700 °C under argon. The formation of a nitrogen-doped carbon layer as an active material on the adsorbent, bonded through a C-Si linkage, has been conclusively verified through elemental composition quantification using XPS and EDX measurements. Two-stage catalytic decomposition and condensation of the adsorbed pesticide is followed by TGA and TPD-MS. Attained carbon-based materials give stable Faradaic capacitance with a slight dependency on the number of adsorbing cycles. Capacitance calculated with respect to the adlayer carbon material reaches values as high as 610 F g−1. Galvanostatic Charge/Discharge measurement confirmed the stability of explored materials with a slight increase in capacitance over 1000 cycles. The presented results envisage electroactive materials preparation from environmental pollutants, adding value to spent adsorbents.",
publisher = "Elsevier B.V.",
journal = "Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy",
title = "Acetamiprid's degradation products and mechanism: Part II – Inert atmosphere and charge storage",
volume = "308",
doi = "10.1016/j.saa.2023.123772"
}

Popadić, D., Krstić, J., Janošević-Ležaić, A., Popović, M., Milojević-Rakić, M., Ignjatović, L., Bajuk-Bogdanović, D.,& Gavrilov, N.. (2024). Acetamiprid's degradation products and mechanism: Part II – Inert atmosphere and charge storage. in Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy
Elsevier B.V.., 308.
https://doi.org/10.1016/j.saa.2023.123772

Popadić D, Krstić J, Janošević-Ležaić A, Popović M, Milojević-Rakić M, Ignjatović L, Bajuk-Bogdanović D, Gavrilov N. Acetamiprid's degradation products and mechanism: Part II – Inert atmosphere and charge storage. in Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy. 2024;308.
doi:10.1016/j.saa.2023.123772 .

Popadić, Daliborka, Krstić, Jugoslav, Janošević-Ležaić, Aleksandra, Popović, Maja, Milojević-Rakić, Maja, Ignjatović, Ljubiša, Bajuk-Bogdanović, Danica, Gavrilov, Nemanja, "Acetamiprid's degradation products and mechanism: Part II – Inert atmosphere and charge storage" in Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy, 308 (2024),
https://doi.org/10.1016/j.saa.2023.123772 . .

TY  - JOUR
AU  - Ranković, Maja
AU  - Jevremović, Anka
AU  - Janošević-Ležaić, Aleksandra
AU  - Arsenijević, Aleksandar
AU  - Rupar, Jelena
AU  - Dobričić, Vladimir
AU  - Nedić Vasiljević, Bojana
AU  - Gavrilov, Nemanja
AU  - Bajuk-Bogdanović, Danica
AU  - Milojević-Rakić, Maja
PY  - 2023
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/4649
AB  - Acridine and its derivatives (9-chloroacridine and 9-aminoacridine) are investigated here, supported on FAU type zeolite Y, as a delivery system of anticancer agents. FTIR/Raman spectroscopy and electron microscopy revealed successful drug loading on the zeolite surface, while spectrofluorimetry was employed for drug quantification. The effects of the tested compounds on cell viability were evaluated using in vitro methylthiazol-tetrazolium (MTT) colorimetric technique against human colorectal carcinoma (cell line HCT-116) and MRC-5 fibroblasts. Zeolite structure remained unchanged during homogeneous drug impregnation with achieved drug loadings in the 18–21 mg/g range. The highest drug release, in the µM concentration range, with favourable kinetics was established for zeolite-supported 9-aminoacridine. The acridine delivery via zeolite carrier is viewed in terms of solvation energy and zeolite adsorption sites. The cytotoxic effect of supported acridines on HCT-116 cells reveals that the zeolite carrier improves toxicity, while the highest efficiency is displayed by zeolite-impregnated 9-aminoacridine. The 9-aminoacridine delivery via zeolite carrier favours healthy tissue preservation while accompanying increased toxicity toward cancer cells. Cytotoxicity results are well correlated with theoretical modelling and release study, providing promising results for applicative purposes.
PB  - MDPI
T2  - Journal of Functional Biomaterials
T1  - Can Zeolite-Supporting Acridines Boost Their Anticancer Performance?
VL  - 14
IS  - 3
DO  - 10.3390/jfb14030173
ER  - 

@article{
author = "Ranković, Maja and Jevremović, Anka and Janošević-Ležaić, Aleksandra and Arsenijević, Aleksandar and Rupar, Jelena and Dobričić, Vladimir and Nedić Vasiljević, Bojana and Gavrilov, Nemanja and Bajuk-Bogdanović, Danica and Milojević-Rakić, Maja",
year = "2023",
abstract = "Acridine and its derivatives (9-chloroacridine and 9-aminoacridine) are investigated here, supported on FAU type zeolite Y, as a delivery system of anticancer agents. FTIR/Raman spectroscopy and electron microscopy revealed successful drug loading on the zeolite surface, while spectrofluorimetry was employed for drug quantification. The effects of the tested compounds on cell viability were evaluated using in vitro methylthiazol-tetrazolium (MTT) colorimetric technique against human colorectal carcinoma (cell line HCT-116) and MRC-5 fibroblasts. Zeolite structure remained unchanged during homogeneous drug impregnation with achieved drug loadings in the 18–21 mg/g range. The highest drug release, in the µM concentration range, with favourable kinetics was established for zeolite-supported 9-aminoacridine. The acridine delivery via zeolite carrier is viewed in terms of solvation energy and zeolite adsorption sites. The cytotoxic effect of supported acridines on HCT-116 cells reveals that the zeolite carrier improves toxicity, while the highest efficiency is displayed by zeolite-impregnated 9-aminoacridine. The 9-aminoacridine delivery via zeolite carrier favours healthy tissue preservation while accompanying increased toxicity toward cancer cells. Cytotoxicity results are well correlated with theoretical modelling and release study, providing promising results for applicative purposes.",
publisher = "MDPI",
journal = "Journal of Functional Biomaterials",
title = "Can Zeolite-Supporting Acridines Boost Their Anticancer Performance?",
volume = "14",
number = "3",
doi = "10.3390/jfb14030173"
}

Ranković, M., Jevremović, A., Janošević-Ležaić, A., Arsenijević, A., Rupar, J., Dobričić, V., Nedić Vasiljević, B., Gavrilov, N., Bajuk-Bogdanović, D.,& Milojević-Rakić, M.. (2023). Can Zeolite-Supporting Acridines Boost Their Anticancer Performance?. in Journal of Functional Biomaterials
MDPI., 14(3).
https://doi.org/10.3390/jfb14030173

Ranković M, Jevremović A, Janošević-Ležaić A, Arsenijević A, Rupar J, Dobričić V, Nedić Vasiljević B, Gavrilov N, Bajuk-Bogdanović D, Milojević-Rakić M. Can Zeolite-Supporting Acridines Boost Their Anticancer Performance?. in Journal of Functional Biomaterials. 2023;14(3).
doi:10.3390/jfb14030173 .

Ranković, Maja, Jevremović, Anka, Janošević-Ležaić, Aleksandra, Arsenijević, Aleksandar, Rupar, Jelena, Dobričić, Vladimir, Nedić Vasiljević, Bojana, Gavrilov, Nemanja, Bajuk-Bogdanović, Danica, Milojević-Rakić, Maja, "Can Zeolite-Supporting Acridines Boost Their Anticancer Performance?" in Journal of Functional Biomaterials, 14, no. 3 (2023),
https://doi.org/10.3390/jfb14030173 . .

TY  - JOUR
AU  - Jevremović, Anka
AU  - Savić, Marjetka
AU  - Janošević-Ležaić, Aleksandra
AU  - Krstić, Jugoslav
AU  - Gavrilov, Nemanja
AU  - Bajuk-Bogdanović, Danica
AU  - Milojević-Rakić, Maja
AU  - Ćirić-Marjanović, Gordana
PY  - 2023
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/5342
AB  - The environmental application of the carbonized composites of the Zn-containing metal-organic framework MOF-5 and polyaniline (PANI) in its emeraldine salt and base forms (C-(MOF-5/PANI)) was investigated for the first time. Textural properties and particle size distributions revealed that composites are dominantly mesoporous and nanoscale in nature, while Raman spectroscopy revealed the ZnO phase beneath the carbon matrix. Adsorption of pesticide, dye, and metal cation on C-(MOF-5/PANI) composites in aqueous solutions was evaluated and compared with the behavior of the precursor components, carbonized MOF-5 (cMOF), and carbonized PANIs. A lower MOF-5 content in the precursor, a higher specific surface area, and the pore volume of the composites led to improved adsorption performance for acetamiprid (124 mg/g) and Methylene Blue (135 mg/g). The presence of O/N functional groups in composites is essential for the adsorption of nitrogen-rich pollutants through hydrogen bonding with an estimated monolayer capacity twice as high as that of cMOF. The proton exchange accompanying Cd2+ retention was associated with the Zn/Cd ion exchange, and the highest capacity (9.8 mg/g) was observed for the composite synthesized from the precursor with a high MOF-5 content. The multifunctionality of composites was evidenced in mixtures of pollutants where noticeably better performance for Cd2+ removal was found for the composite compared to cMOF. Competitive binding between three pollutants favored the adsorption of pesticide and dye, thereby hindering to some extent the ion exchange necessary for the removal of metal cations. The results emphasize the importance of the PANI form and MOF-5/PANI weight ratio in precursors for the development of surface, porosity, and active sites in C-(MOF-5/PANI) composites, thus guiding their environmental efficiency. The study also demonstrated that C-(MOF-5/PANI) composites retained studied pollutants much better than carbonized precursor PANIs and showed comparable or better adsorption ability than cMOF.
PB  - MDPI
T2  - Polymers
T1  - Environmental Potential of Carbonized MOF-5/PANI Composites for Pesticide, Dye, and Metal Cations—Can They Actually Retain Them All?
VL  - 15
IS  - 22
DO  - 10.3390/polym15224349
ER  - 

@article{
author = "Jevremović, Anka and Savić, Marjetka and Janošević-Ležaić, Aleksandra and Krstić, Jugoslav and Gavrilov, Nemanja and Bajuk-Bogdanović, Danica and Milojević-Rakić, Maja and Ćirić-Marjanović, Gordana",
year = "2023",
abstract = "The environmental application of the carbonized composites of the Zn-containing metal-organic framework MOF-5 and polyaniline (PANI) in its emeraldine salt and base forms (C-(MOF-5/PANI)) was investigated for the first time. Textural properties and particle size distributions revealed that composites are dominantly mesoporous and nanoscale in nature, while Raman spectroscopy revealed the ZnO phase beneath the carbon matrix. Adsorption of pesticide, dye, and metal cation on C-(MOF-5/PANI) composites in aqueous solutions was evaluated and compared with the behavior of the precursor components, carbonized MOF-5 (cMOF), and carbonized PANIs. A lower MOF-5 content in the precursor, a higher specific surface area, and the pore volume of the composites led to improved adsorption performance for acetamiprid (124 mg/g) and Methylene Blue (135 mg/g). The presence of O/N functional groups in composites is essential for the adsorption of nitrogen-rich pollutants through hydrogen bonding with an estimated monolayer capacity twice as high as that of cMOF. The proton exchange accompanying Cd2+ retention was associated with the Zn/Cd ion exchange, and the highest capacity (9.8 mg/g) was observed for the composite synthesized from the precursor with a high MOF-5 content. The multifunctionality of composites was evidenced in mixtures of pollutants where noticeably better performance for Cd2+ removal was found for the composite compared to cMOF. Competitive binding between three pollutants favored the adsorption of pesticide and dye, thereby hindering to some extent the ion exchange necessary for the removal of metal cations. The results emphasize the importance of the PANI form and MOF-5/PANI weight ratio in precursors for the development of surface, porosity, and active sites in C-(MOF-5/PANI) composites, thus guiding their environmental efficiency. The study also demonstrated that C-(MOF-5/PANI) composites retained studied pollutants much better than carbonized precursor PANIs and showed comparable or better adsorption ability than cMOF.",
publisher = "MDPI",
journal = "Polymers",
title = "Environmental Potential of Carbonized MOF-5/PANI Composites for Pesticide, Dye, and Metal Cations—Can They Actually Retain Them All?",
volume = "15",
number = "22",
doi = "10.3390/polym15224349"
}

Jevremović, A., Savić, M., Janošević-Ležaić, A., Krstić, J., Gavrilov, N., Bajuk-Bogdanović, D., Milojević-Rakić, M.,& Ćirić-Marjanović, G.. (2023). Environmental Potential of Carbonized MOF-5/PANI Composites for Pesticide, Dye, and Metal Cations—Can They Actually Retain Them All?. in Polymers
MDPI., 15(22).
https://doi.org/10.3390/polym15224349

Jevremović A, Savić M, Janošević-Ležaić A, Krstić J, Gavrilov N, Bajuk-Bogdanović D, Milojević-Rakić M, Ćirić-Marjanović G. Environmental Potential of Carbonized MOF-5/PANI Composites for Pesticide, Dye, and Metal Cations—Can They Actually Retain Them All?. in Polymers. 2023;15(22).
doi:10.3390/polym15224349 .

Jevremović, Anka, Savić, Marjetka, Janošević-Ležaić, Aleksandra, Krstić, Jugoslav, Gavrilov, Nemanja, Bajuk-Bogdanović, Danica, Milojević-Rakić, Maja, Ćirić-Marjanović, Gordana, "Environmental Potential of Carbonized MOF-5/PANI Composites for Pesticide, Dye, and Metal Cations—Can They Actually Retain Them All?" in Polymers, 15, no. 22 (2023),
https://doi.org/10.3390/polym15224349 . .

TY  - JOUR
AU  - Rupar, Jelena
AU  - Hrnjić, Armin
AU  - Uskoković-Marković, Snežana
AU  - Bajuk-Bogdanović, Danica
AU  - Milojević-Rakić, Maja
AU  - Gavrilov, Nemanja
AU  - Janošević-Ležaić, Aleksandra
PY  - 2023
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/4989
AB  - Electrochemical crosslinking of alginate strands by in situ iron oxidation was explored using a potentiostatic regime. Carbon-based materials co-doped with iron, nitrogen, and/or sulfur were prepared via electrolyte composition variation with a nitrogen-rich compound (rivanol) or through post-treatments with sodium sulfide. Nanometer-sized iron particles were confirmed by transmission and field emission scanning electron microscopy in all samples as a consequence of the homogeneous dispersion of iron in the alginate scaffold and its concomitant growth-limiting effect of alginate chains. Raman spectra confirmed a rise in structural disorder with rivanol/Na2S treatment, which points to more defect sites and edges known to be active sites for oxygen reduction. Fourier transform infrared (FTIR) spectra confirmed the presence of different iron, nitrogen, and sulfur species, with a marked difference between Na2S treated/untreated samples. The most positive onset potential (−0.26 V vs. saturated calomel electrode, SCE) was evidenced for the sample co-doped with N, S, and Fe, surpassing the activity of those with single and/or double doping. The mechanism of oxygen reduction in 0.1 M KOH was dominated by the 2e− reduction pathway at low overpotentials and shifted towards complete 4e− reduction at the most negative explored values. The presented results put forward electrochemically formed alginate gels functionalized by homogeneously dispersed multivalent cations as an excellent starting point in nanomaterial design and engineering.
PB  - MDPI
T2  - Polymers
T1  - Electrochemical Crosslinking of Alginate—Towards Doped Carbons for Oxygen Reduction
VL  - 15
IS  - 15
DO  - 10.3390/polym15153169
ER  - 

@article{
author = "Rupar, Jelena and Hrnjić, Armin and Uskoković-Marković, Snežana and Bajuk-Bogdanović, Danica and Milojević-Rakić, Maja and Gavrilov, Nemanja and Janošević-Ležaić, Aleksandra",
year = "2023",
abstract = "Electrochemical crosslinking of alginate strands by in situ iron oxidation was explored using a potentiostatic regime. Carbon-based materials co-doped with iron, nitrogen, and/or sulfur were prepared via electrolyte composition variation with a nitrogen-rich compound (rivanol) or through post-treatments with sodium sulfide. Nanometer-sized iron particles were confirmed by transmission and field emission scanning electron microscopy in all samples as a consequence of the homogeneous dispersion of iron in the alginate scaffold and its concomitant growth-limiting effect of alginate chains. Raman spectra confirmed a rise in structural disorder with rivanol/Na2S treatment, which points to more defect sites and edges known to be active sites for oxygen reduction. Fourier transform infrared (FTIR) spectra confirmed the presence of different iron, nitrogen, and sulfur species, with a marked difference between Na2S treated/untreated samples. The most positive onset potential (−0.26 V vs. saturated calomel electrode, SCE) was evidenced for the sample co-doped with N, S, and Fe, surpassing the activity of those with single and/or double doping. The mechanism of oxygen reduction in 0.1 M KOH was dominated by the 2e− reduction pathway at low overpotentials and shifted towards complete 4e− reduction at the most negative explored values. The presented results put forward electrochemically formed alginate gels functionalized by homogeneously dispersed multivalent cations as an excellent starting point in nanomaterial design and engineering.",
publisher = "MDPI",
journal = "Polymers",
title = "Electrochemical Crosslinking of Alginate—Towards Doped Carbons for Oxygen Reduction",
volume = "15",
number = "15",
doi = "10.3390/polym15153169"
}

Rupar, J., Hrnjić, A., Uskoković-Marković, S., Bajuk-Bogdanović, D., Milojević-Rakić, M., Gavrilov, N.,& Janošević-Ležaić, A.. (2023). Electrochemical Crosslinking of Alginate—Towards Doped Carbons for Oxygen Reduction. in Polymers
MDPI., 15(15).
https://doi.org/10.3390/polym15153169

Rupar J, Hrnjić A, Uskoković-Marković S, Bajuk-Bogdanović D, Milojević-Rakić M, Gavrilov N, Janošević-Ležaić A. Electrochemical Crosslinking of Alginate—Towards Doped Carbons for Oxygen Reduction. in Polymers. 2023;15(15).
doi:10.3390/polym15153169 .

Rupar, Jelena, Hrnjić, Armin, Uskoković-Marković, Snežana, Bajuk-Bogdanović, Danica, Milojević-Rakić, Maja, Gavrilov, Nemanja, Janošević-Ležaić, Aleksandra, "Electrochemical Crosslinking of Alginate—Towards Doped Carbons for Oxygen Reduction" in Polymers, 15, no. 15 (2023),
https://doi.org/10.3390/polym15153169 . .

TY  - JOUR
AU  - Popadić, Daliborka
AU  - Gavrilov, Nemanja
AU  - Krstić, Jugoslav
AU  - Nedić Vasiljević, Bojana
AU  - Janošević-Ležaić, Aleksandra
AU  - Uskoković-Marković, Snežana
AU  - Milojević-Rakić, Maja
AU  - Bajuk-Bogdanović, Danica
PY  - 2023
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/4882
AB  - Herein we unequivocally identify the mechanism of zeolite-catalysed thermal degradation of pesticide, employing Fourier-transform infrared spectroscopy (FTIR), Raman and mass spectrometry following temperature decomposition (TPDe/MS). We demonstrate that Y zeolite can effectively adsorb a significant amount of acetamiprid both in a single trial (168 mg/g) and in 10 cycles (1249 mg/g) with intermittent thermal regeneration at 300 °C. Sectional vibrational analysis of acetamiprid two-stage thermal degradation is performed for pristine and supported pesticide. The acetamiprid Raman spectral changes appear at 200 °C, while partial carbonization occurs at 250 °C. The gradual disappearance of the FTIR bands of acetamiprid is seen up to 270 °C when two Raman signature bands for carbonised material emerged. The TPDe/MS profiles reveal the evolution of mass fragments - in the first step, cleavage of the C[sbnd]C bond occurs between the aromatic core of the molecule and its tail-end, followed by cleavage of the C[sbnd]N bond. The mechanism of adsorbed acetamiprid degradation follows the same step, at significantly lower temperatures, as the process is catalysed by the interaction of acetamiprid nitrogens and zeolite support. Reduced temperature degradation allows for a quick recovery process that leaves 65% efficacy after 10 cycles. After numerous cycles of recovery, a subsequent one-time heat treatment at 700 °C completely restores initial efficacy. The efficient adsorption, novel details on degradation mechanism and ease of regeneration procedure place the Y zeolite at the forefront of future all-encompassing environmental solutions.
PB  - Elsevier B.V.
T2  - Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy
T1  - Spectral evidence of acetamiprid's thermal degradation products and mechanism
VL  - 301
IS  - 15
DO  - 10.1016/j.saa.2023.122987
ER  - 

@article{
author = "Popadić, Daliborka and Gavrilov, Nemanja and Krstić, Jugoslav and Nedić Vasiljević, Bojana and Janošević-Ležaić, Aleksandra and Uskoković-Marković, Snežana and Milojević-Rakić, Maja and Bajuk-Bogdanović, Danica",
year = "2023",
abstract = "Herein we unequivocally identify the mechanism of zeolite-catalysed thermal degradation of pesticide, employing Fourier-transform infrared spectroscopy (FTIR), Raman and mass spectrometry following temperature decomposition (TPDe/MS). We demonstrate that Y zeolite can effectively adsorb a significant amount of acetamiprid both in a single trial (168 mg/g) and in 10 cycles (1249 mg/g) with intermittent thermal regeneration at 300 °C. Sectional vibrational analysis of acetamiprid two-stage thermal degradation is performed for pristine and supported pesticide. The acetamiprid Raman spectral changes appear at 200 °C, while partial carbonization occurs at 250 °C. The gradual disappearance of the FTIR bands of acetamiprid is seen up to 270 °C when two Raman signature bands for carbonised material emerged. The TPDe/MS profiles reveal the evolution of mass fragments - in the first step, cleavage of the C[sbnd]C bond occurs between the aromatic core of the molecule and its tail-end, followed by cleavage of the C[sbnd]N bond. The mechanism of adsorbed acetamiprid degradation follows the same step, at significantly lower temperatures, as the process is catalysed by the interaction of acetamiprid nitrogens and zeolite support. Reduced temperature degradation allows for a quick recovery process that leaves 65% efficacy after 10 cycles. After numerous cycles of recovery, a subsequent one-time heat treatment at 700 °C completely restores initial efficacy. The efficient adsorption, novel details on degradation mechanism and ease of regeneration procedure place the Y zeolite at the forefront of future all-encompassing environmental solutions.",
publisher = "Elsevier B.V.",
journal = "Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy",
title = "Spectral evidence of acetamiprid's thermal degradation products and mechanism",
volume = "301",
number = "15",
doi = "10.1016/j.saa.2023.122987"
}

Popadić, D., Gavrilov, N., Krstić, J., Nedić Vasiljević, B., Janošević-Ležaić, A., Uskoković-Marković, S., Milojević-Rakić, M.,& Bajuk-Bogdanović, D.. (2023). Spectral evidence of acetamiprid's thermal degradation products and mechanism. in Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy
Elsevier B.V.., 301(15).
https://doi.org/10.1016/j.saa.2023.122987

Popadić D, Gavrilov N, Krstić J, Nedić Vasiljević B, Janošević-Ležaić A, Uskoković-Marković S, Milojević-Rakić M, Bajuk-Bogdanović D. Spectral evidence of acetamiprid's thermal degradation products and mechanism. in Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy. 2023;301(15).
doi:10.1016/j.saa.2023.122987 .

Popadić, Daliborka, Gavrilov, Nemanja, Krstić, Jugoslav, Nedić Vasiljević, Bojana, Janošević-Ležaić, Aleksandra, Uskoković-Marković, Snežana, Milojević-Rakić, Maja, Bajuk-Bogdanović, Danica, "Spectral evidence of acetamiprid's thermal degradation products and mechanism" in Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy, 301, no. 15 (2023),
https://doi.org/10.1016/j.saa.2023.122987 . .

TY  - JOUR
AU  - Rupar, Jelena
AU  - Bajuk-Bogdanović, Danica
AU  - Milojević-Rakić, Maja
AU  - Krstić, Jugoslav
AU  - Upadhyay, Kush
AU  - Gavrilov, Nemanja
AU  - Janošević-Ležaić, Aleksandra
PY  - 2022
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/4069
AB  - Here, we propose a novel, electrochemical preparation of in situ N-doped alginate-based carbon precursors with monodispersed zinc ions. Obtained carbons were evaluated by spectroscopic (FTIR, Raman and XPS), textural (N2 physisorption), microscopic (TEM) and elemental (SEM-EDS) descriptors to establish their distinctive fea- tures originating from different synthetic procedures. Carbons characteristics were assessed in view of several carbonization temperatures applied for their preparation from alginate precursors, and individual and joint effect of zinc and nitrogen on the precursor. Obtained Zn monodispersion, emphasizes the significance of electro- chemical preparation, allowing increasing temperature to induce changes from its ionic form to carbonate and oxide, while at 800 ◦C ZnO further reduces and evaporates. Since homogeneously dispersed Zn species acts as porosity evolving agent during carbonization, a substantial surface area is developed, in the range 718–1056 m2 g
PB  - Elsevier B.V.
T2  - Microporous and Mesoporous Materials
T1  - Tailored porosity development in carbons via Zn2+ monodispersion: Fitting supercapacitors
VL  - 335
DO  - 10.1016/j.micromeso.2022.111790
ER  - 

@article{
author = "Rupar, Jelena and Bajuk-Bogdanović, Danica and Milojević-Rakić, Maja and Krstić, Jugoslav and Upadhyay, Kush and Gavrilov, Nemanja and Janošević-Ležaić, Aleksandra",
year = "2022",
abstract = "Here, we propose a novel, electrochemical preparation of in situ N-doped alginate-based carbon precursors with monodispersed zinc ions. Obtained carbons were evaluated by spectroscopic (FTIR, Raman and XPS), textural (N2 physisorption), microscopic (TEM) and elemental (SEM-EDS) descriptors to establish their distinctive fea- tures originating from different synthetic procedures. Carbons characteristics were assessed in view of several carbonization temperatures applied for their preparation from alginate precursors, and individual and joint effect of zinc and nitrogen on the precursor. Obtained Zn monodispersion, emphasizes the significance of electro- chemical preparation, allowing increasing temperature to induce changes from its ionic form to carbonate and oxide, while at 800 ◦C ZnO further reduces and evaporates. Since homogeneously dispersed Zn species acts as porosity evolving agent during carbonization, a substantial surface area is developed, in the range 718–1056 m2 g",
publisher = "Elsevier B.V.",
journal = "Microporous and Mesoporous Materials",
title = "Tailored porosity development in carbons via Zn2+ monodispersion: Fitting supercapacitors",
volume = "335",
doi = "10.1016/j.micromeso.2022.111790"
}

Rupar, J., Bajuk-Bogdanović, D., Milojević-Rakić, M., Krstić, J., Upadhyay, K., Gavrilov, N.,& Janošević-Ležaić, A.. (2022). Tailored porosity development in carbons via Zn2+ monodispersion: Fitting supercapacitors. in Microporous and Mesoporous Materials
Elsevier B.V.., 335.
https://doi.org/10.1016/j.micromeso.2022.111790

Rupar J, Bajuk-Bogdanović D, Milojević-Rakić M, Krstić J, Upadhyay K, Gavrilov N, Janošević-Ležaić A. Tailored porosity development in carbons via Zn2+ monodispersion: Fitting supercapacitors. in Microporous and Mesoporous Materials. 2022;335.
doi:10.1016/j.micromeso.2022.111790 .

Rupar, Jelena, Bajuk-Bogdanović, Danica, Milojević-Rakić, Maja, Krstić, Jugoslav, Upadhyay, Kush, Gavrilov, Nemanja, Janošević-Ležaić, Aleksandra, "Tailored porosity development in carbons via Zn2+ monodispersion: Fitting supercapacitors" in Microporous and Mesoporous Materials, 335 (2022),
https://doi.org/10.1016/j.micromeso.2022.111790 . .

TY  - JOUR
AU  - Milojević-Rakić, Maja
AU  - Popadić, Daliborka
AU  - Janošević-Ležaić, Aleksandra
AU  - Jevremović, Anka
AU  - Nedić-Vasiljević, Bojana
AU  - Uskoković-Marković, Snežana
AU  - Bajuk-Bogdanović, Danica
PY  - 2022
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/4062
AB  - Ecotoxicity caused by neonicotinoid pesticides is largely due to oxidative stress on non-target species. Due to the fact that reactive radical species reach the environment, materials intended for pesticide removal should be applicable for the simultaneous removal of reactive radicals, as well. This work uses the spectroscopic, adsorptive and antioxidant responses from MFI, FAU and BEA zeolites as descriptors of their potential environmental importance. Different network structures and Si/Al ratios were correlated with excellent zeolite adsorption properties, as over 200 mg g1 of investigated neonicotinoids, acetamiprid and imidacloprid, was achieved in one cycle. Additionally, after two regeneration steps, over 450 mg g1 adsorbed pesticides were retained, in three adsorption cycles. Overall the best results were detected for the FAU zeotype in both tested applications, insecticide adsorption and radical-scavenging performance, with and without insecticides present. The proposed mechanism for adsorption relies on kinetic investigation, isotherm modelling and spectroscopic post-adsorption analysis and targets zeolite hydroxyl/siloxane groups as active sites for insecticide adsorption via hydrogen bonding. Neat, welldefined zeolite structures enable their prospective application in ecotoxic species removal.
PB  - The Royal Society of Chemistry
T2  - Environmental science. Processes & impacts
T1  - MFI, BEA and FAU zeolite scavenging role in neonicotinoids and radical species elimination
VL  - 24
IS  - 2
SP  - 265
EP  - 276
DO  - 10.1039/d1em00437a
ER  - 

@article{
author = "Milojević-Rakić, Maja and Popadić, Daliborka and Janošević-Ležaić, Aleksandra and Jevremović, Anka and Nedić-Vasiljević, Bojana and Uskoković-Marković, Snežana and Bajuk-Bogdanović, Danica",
year = "2022",
abstract = "Ecotoxicity caused by neonicotinoid pesticides is largely due to oxidative stress on non-target species. Due to the fact that reactive radical species reach the environment, materials intended for pesticide removal should be applicable for the simultaneous removal of reactive radicals, as well. This work uses the spectroscopic, adsorptive and antioxidant responses from MFI, FAU and BEA zeolites as descriptors of their potential environmental importance. Different network structures and Si/Al ratios were correlated with excellent zeolite adsorption properties, as over 200 mg g1 of investigated neonicotinoids, acetamiprid and imidacloprid, was achieved in one cycle. Additionally, after two regeneration steps, over 450 mg g1 adsorbed pesticides were retained, in three adsorption cycles. Overall the best results were detected for the FAU zeotype in both tested applications, insecticide adsorption and radical-scavenging performance, with and without insecticides present. The proposed mechanism for adsorption relies on kinetic investigation, isotherm modelling and spectroscopic post-adsorption analysis and targets zeolite hydroxyl/siloxane groups as active sites for insecticide adsorption via hydrogen bonding. Neat, welldefined zeolite structures enable their prospective application in ecotoxic species removal.",
publisher = "The Royal Society of Chemistry",
journal = "Environmental science. Processes & impacts",
title = "MFI, BEA and FAU zeolite scavenging role in neonicotinoids and radical species elimination",
volume = "24",
number = "2",
pages = "265-276",
doi = "10.1039/d1em00437a"
}

Milojević-Rakić, M., Popadić, D., Janošević-Ležaić, A., Jevremović, A., Nedić-Vasiljević, B., Uskoković-Marković, S.,& Bajuk-Bogdanović, D.. (2022). MFI, BEA and FAU zeolite scavenging role in neonicotinoids and radical species elimination. in Environmental science. Processes & impacts
The Royal Society of Chemistry., 24(2), 265-276.
https://doi.org/10.1039/d1em00437a

Milojević-Rakić M, Popadić D, Janošević-Ležaić A, Jevremović A, Nedić-Vasiljević B, Uskoković-Marković S, Bajuk-Bogdanović D. MFI, BEA and FAU zeolite scavenging role in neonicotinoids and radical species elimination. in Environmental science. Processes & impacts. 2022;24(2):265-276.
doi:10.1039/d1em00437a .

Milojević-Rakić, Maja, Popadić, Daliborka, Janošević-Ležaić, Aleksandra, Jevremović, Anka, Nedić-Vasiljević, Bojana, Uskoković-Marković, Snežana, Bajuk-Bogdanović, Danica, "MFI, BEA and FAU zeolite scavenging role in neonicotinoids and radical species elimination" in Environmental science. Processes & impacts, 24, no. 2 (2022):265-276,
https://doi.org/10.1039/d1em00437a . .

TY  - JOUR
AU  - Popadić, Daliborka
AU  - Gavrilov, Nemanja
AU  - Ignjatović, Ljubiša
AU  - Krajišnik, Danina
AU  - Mentus, Slavko
AU  - Milojević-Rakić, Maja
AU  - Bajuk-Bogdanović, Danica
PY  - 2022
UR  - https://www.mdpi.com/2073-4344/12/5/519
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/4099
AB  - Unmodified natural silicates (bentonite, kaolin, clinoptilolite and diatomites) were tested as adsorbents for the organic pollutants in water tables using Methylene Blue (MB) as the model adsorbate. Among the selected materials, bentonite adsorbed as much as 237 mg/g, confirming its excellent suitability for pollutant removal. Spectral evidence confirmed successful MB immobilization at the bentonite surface. Furthermore, the thermal treatment of MB-saturated adsorbent in an inert atmosphere at 700 °C produced a carbon/silicate composite. EDX confirmed the formation of the nitrogen-doped carbon overlay on the silica scaffold and the obtained composite material was probed as an electrode material for oxygen reduction in an alkaline solution. Reduction proceeded via a two-electron mechanism with the main product being HO2−, a known nucleophile, which was subsequently used to degrade/demethylate MB. The composite showed a considerable 70% MB removal rate after an hour of electrochemical treatment. The synergy between the processes of adsorption of MB and the surface-generated HO2− dictates the efficiency of the method and points to a possible route for spent adsorbent reuse in the form of a durable product for environmental protection.
PB  - MDPI
T2  - Catalysts
T1  - How to Obtain Maximum Environmental Applicability from Natural Silicates
VL  - 12
IS  - 5
DO  - 10.3390/catal12050519
ER  - 

@article{
author = "Popadić, Daliborka and Gavrilov, Nemanja and Ignjatović, Ljubiša and Krajišnik, Danina and Mentus, Slavko and Milojević-Rakić, Maja and Bajuk-Bogdanović, Danica",
year = "2022",
abstract = "Unmodified natural silicates (bentonite, kaolin, clinoptilolite and diatomites) were tested as adsorbents for the organic pollutants in water tables using Methylene Blue (MB) as the model adsorbate. Among the selected materials, bentonite adsorbed as much as 237 mg/g, confirming its excellent suitability for pollutant removal. Spectral evidence confirmed successful MB immobilization at the bentonite surface. Furthermore, the thermal treatment of MB-saturated adsorbent in an inert atmosphere at 700 °C produced a carbon/silicate composite. EDX confirmed the formation of the nitrogen-doped carbon overlay on the silica scaffold and the obtained composite material was probed as an electrode material for oxygen reduction in an alkaline solution. Reduction proceeded via a two-electron mechanism with the main product being HO2−, a known nucleophile, which was subsequently used to degrade/demethylate MB. The composite showed a considerable 70% MB removal rate after an hour of electrochemical treatment. The synergy between the processes of adsorption of MB and the surface-generated HO2− dictates the efficiency of the method and points to a possible route for spent adsorbent reuse in the form of a durable product for environmental protection.",
publisher = "MDPI",
journal = "Catalysts",
title = "How to Obtain Maximum Environmental Applicability from Natural Silicates",
volume = "12",
number = "5",
doi = "10.3390/catal12050519"
}

Popadić, D., Gavrilov, N., Ignjatović, L., Krajišnik, D., Mentus, S., Milojević-Rakić, M.,& Bajuk-Bogdanović, D.. (2022). How to Obtain Maximum Environmental Applicability from Natural Silicates. in Catalysts
MDPI., 12(5).
https://doi.org/10.3390/catal12050519

Popadić D, Gavrilov N, Ignjatović L, Krajišnik D, Mentus S, Milojević-Rakić M, Bajuk-Bogdanović D. How to Obtain Maximum Environmental Applicability from Natural Silicates. in Catalysts. 2022;12(5).
doi:10.3390/catal12050519 .

Popadić, Daliborka, Gavrilov, Nemanja, Ignjatović, Ljubiša, Krajišnik, Danina, Mentus, Slavko, Milojević-Rakić, Maja, Bajuk-Bogdanović, Danica, "How to Obtain Maximum Environmental Applicability from Natural Silicates" in Catalysts, 12, no. 5 (2022),
https://doi.org/10.3390/catal12050519 . .

TY  - JOUR
AU  - Janićijević, Dejana
AU  - Jevremović, Anka
AU  - Janošević-Ležaić, Aleksandra
AU  - Nedić-Vasiljević, Bojana
AU  - Uskoković-Marković, Snežana
AU  - Bajuk-Bogdanović, Danica
AU  - Milojević-Rakić, Maja
PY  - 2021
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3970
AB  - Composite materials consisting of the silver salt of dodecatungstophosphoric acid and HBEA zeolite are developed in order to give materials of superior adsorption properties for aqueous pesticide removal. Two-step impregnation and an ion-exchange method with variable constituent mass ratios were employed as synthesis procedures. One of the study goals was to optimize the composite preparation for efficient elimination of glyphosate pesticide and to investigate the modulation of antioxidant activity in the presence of pesticide. Based on comprehensive results, we propose mechanisms for simultaneous glyphosate removal and antioxidant activity. Spectroscopic analysis shows that the applied two-step impregnation method results in advanced composite materials with evenly distributed active sites for glyphosate adsorption and radical-scavenging activity. The original Krishnamurti isotherm is successfully used to fit pesticide adsorption data, pointing to co-operative adsorption of glyphosate on partly saturated adsorbents sites. The amount of glyphosate adsorbed from water suspension was 378 mg per gram of composite material, the highest value reported for glyphosate removal to date.
PB  - Elsevier Ltd
T2  - Journal of Environmental Chemical Engineering
T1  - Comparative assessment of pesticide adsorption capacity and antioxidant activity of Silver Dodecatungstophosphate/HΒEA zeolite composites
VL  - 9
IS  - 6
DO  - 10.1016/j.jece.2021.106341
ER  - 

@article{
author = "Janićijević, Dejana and Jevremović, Anka and Janošević-Ležaić, Aleksandra and Nedić-Vasiljević, Bojana and Uskoković-Marković, Snežana and Bajuk-Bogdanović, Danica and Milojević-Rakić, Maja",
year = "2021",
abstract = "Composite materials consisting of the silver salt of dodecatungstophosphoric acid and HBEA zeolite are developed in order to give materials of superior adsorption properties for aqueous pesticide removal. Two-step impregnation and an ion-exchange method with variable constituent mass ratios were employed as synthesis procedures. One of the study goals was to optimize the composite preparation for efficient elimination of glyphosate pesticide and to investigate the modulation of antioxidant activity in the presence of pesticide. Based on comprehensive results, we propose mechanisms for simultaneous glyphosate removal and antioxidant activity. Spectroscopic analysis shows that the applied two-step impregnation method results in advanced composite materials with evenly distributed active sites for glyphosate adsorption and radical-scavenging activity. The original Krishnamurti isotherm is successfully used to fit pesticide adsorption data, pointing to co-operative adsorption of glyphosate on partly saturated adsorbents sites. The amount of glyphosate adsorbed from water suspension was 378 mg per gram of composite material, the highest value reported for glyphosate removal to date.",
publisher = "Elsevier Ltd",
journal = "Journal of Environmental Chemical Engineering",
title = "Comparative assessment of pesticide adsorption capacity and antioxidant activity of Silver Dodecatungstophosphate/HΒEA zeolite composites",
volume = "9",
number = "6",
doi = "10.1016/j.jece.2021.106341"
}

Janićijević, D., Jevremović, A., Janošević-Ležaić, A., Nedić-Vasiljević, B., Uskoković-Marković, S., Bajuk-Bogdanović, D.,& Milojević-Rakić, M.. (2021). Comparative assessment of pesticide adsorption capacity and antioxidant activity of Silver Dodecatungstophosphate/HΒEA zeolite composites. in Journal of Environmental Chemical Engineering
Elsevier Ltd., 9(6).
https://doi.org/10.1016/j.jece.2021.106341

Janićijević D, Jevremović A, Janošević-Ležaić A, Nedić-Vasiljević B, Uskoković-Marković S, Bajuk-Bogdanović D, Milojević-Rakić M. Comparative assessment of pesticide adsorption capacity and antioxidant activity of Silver Dodecatungstophosphate/HΒEA zeolite composites. in Journal of Environmental Chemical Engineering. 2021;9(6).
doi:10.1016/j.jece.2021.106341 .

Janićijević, Dejana, Jevremović, Anka, Janošević-Ležaić, Aleksandra, Nedić-Vasiljević, Bojana, Uskoković-Marković, Snežana, Bajuk-Bogdanović, Danica, Milojević-Rakić, Maja, "Comparative assessment of pesticide adsorption capacity and antioxidant activity of Silver Dodecatungstophosphate/HΒEA zeolite composites" in Journal of Environmental Chemical Engineering, 9, no. 6 (2021),
https://doi.org/10.1016/j.jece.2021.106341 . .

TY  - JOUR
AU  - Janićijević, Dejana
AU  - Uskoković-Marković, Snežana
AU  - Popa, Alexandru
AU  - Nedić-Vasiljević, Bojana
AU  - Jevremović, Anka
AU  - Milojević-Rakić, Maja
AU  - Bajuk-Bogdanović, Danica
PY  - 2021
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3792
AB  - Heteropolyacids and their salts comprise catalytic centers for the production of ethylene, one of the most important constituents in the chemical industry. The paper emphasizes different synthesis routes of hybrid materials consisting of dodecatungstophosphoric acid silver salt (AgPW) and β zeolite—stepwise wet impregnation, silver-exchange in β zeolite, and dry mixing of precursors. Composite preparation procedures induced minor effects on the weak acid sites, while strong acid sites were increased significantly. β/AgPW composites prepared by two-steps wet impregnation and ion-exchange procedures have strong acid sites content and total acidity higher in comparison to the pure AgPW salt and β zeolite. This is a result of precursors synergetic effect—cumulative strong acidic sites are generated in the presence of well-dispersed Keggin ions on the zeolite network. Composite samples with a higher content of strong acid centers exhibit higher conversion in the ethanol dehydration reaction, i.e., the ion-exchanged βAgPW sample has attained a conversion over 81%, while the wet-impregnated sample has a significant 86%. The distribution and presence of AgPW active phase are found to be crucial for both stable conversion and high selectivity results in ethylene production from ethanol, which is regarded as one of the most significant processes in environmental and sustainable industrial chemistry. Graphic abstract: [Figure not available: see fulltext.]
PB  - Springer Science and Business Media Deutschland GmbH
T2  - Chemical Papers
T1  - The impact of preparation route on the performance of silver dodecatungstophosphate/β zeolite catalysts in the ethylene production
VL  - 75
SP  - 3169
EP  - 3180
DO  - 10.1007/s11696-021-01557-3
ER  - 

@article{
author = "Janićijević, Dejana and Uskoković-Marković, Snežana and Popa, Alexandru and Nedić-Vasiljević, Bojana and Jevremović, Anka and Milojević-Rakić, Maja and Bajuk-Bogdanović, Danica",
year = "2021",
abstract = "Heteropolyacids and their salts comprise catalytic centers for the production of ethylene, one of the most important constituents in the chemical industry. The paper emphasizes different synthesis routes of hybrid materials consisting of dodecatungstophosphoric acid silver salt (AgPW) and β zeolite—stepwise wet impregnation, silver-exchange in β zeolite, and dry mixing of precursors. Composite preparation procedures induced minor effects on the weak acid sites, while strong acid sites were increased significantly. β/AgPW composites prepared by two-steps wet impregnation and ion-exchange procedures have strong acid sites content and total acidity higher in comparison to the pure AgPW salt and β zeolite. This is a result of precursors synergetic effect—cumulative strong acidic sites are generated in the presence of well-dispersed Keggin ions on the zeolite network. Composite samples with a higher content of strong acid centers exhibit higher conversion in the ethanol dehydration reaction, i.e., the ion-exchanged βAgPW sample has attained a conversion over 81%, while the wet-impregnated sample has a significant 86%. The distribution and presence of AgPW active phase are found to be crucial for both stable conversion and high selectivity results in ethylene production from ethanol, which is regarded as one of the most significant processes in environmental and sustainable industrial chemistry. Graphic abstract: [Figure not available: see fulltext.]",
publisher = "Springer Science and Business Media Deutschland GmbH",
journal = "Chemical Papers",
title = "The impact of preparation route on the performance of silver dodecatungstophosphate/β zeolite catalysts in the ethylene production",
volume = "75",
pages = "3169-3180",
doi = "10.1007/s11696-021-01557-3"
}

Janićijević, D., Uskoković-Marković, S., Popa, A., Nedić-Vasiljević, B., Jevremović, A., Milojević-Rakić, M.,& Bajuk-Bogdanović, D.. (2021). The impact of preparation route on the performance of silver dodecatungstophosphate/β zeolite catalysts in the ethylene production. in Chemical Papers
Springer Science and Business Media Deutschland GmbH., 75, 3169-3180.
https://doi.org/10.1007/s11696-021-01557-3

Janićijević D, Uskoković-Marković S, Popa A, Nedić-Vasiljević B, Jevremović A, Milojević-Rakić M, Bajuk-Bogdanović D. The impact of preparation route on the performance of silver dodecatungstophosphate/β zeolite catalysts in the ethylene production. in Chemical Papers. 2021;75:3169-3180.
doi:10.1007/s11696-021-01557-3 .

Janićijević, Dejana, Uskoković-Marković, Snežana, Popa, Alexandru, Nedić-Vasiljević, Bojana, Jevremović, Anka, Milojević-Rakić, Maja, Bajuk-Bogdanović, Danica, "The impact of preparation route on the performance of silver dodecatungstophosphate/β zeolite catalysts in the ethylene production" in Chemical Papers, 75 (2021):3169-3180,
https://doi.org/10.1007/s11696-021-01557-3 . .

TY  - JOUR
AU  - Jevremović, Anka
AU  - Nedić-Vasiljević, Bojana
AU  - Popa, Alexandru
AU  - Uskoković-Marković, Snežana
AU  - Ignjatović, Ljubiša
AU  - Bajuk-Bogdanović, Danica
AU  - Milojević-Rakić, Maja
PY  - 2021
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3783
AB  - Environmental implementation of novel composite materials comprising potassium tungstophosphate (KPW) and ZSM-5 zeolite was tested in ethene production and pesticide removal. The study revealed that the binding of KPW to ZSM-5 zeolites of different Si/Al ratios affects the formation of active centres for catalytic and adsorption processes. Brønsted active sites present in the zeolite framework are synergistically joined with Lewis centres and additional Brønsted centres through the impregnation of potassium tungstophosphate, which resulted in improvement of stability and activity of investigated materials. Adsorption and catalytic performance were found to be influenced by the order of addition of salt precursors and by post-synthesis thermal treatment. The best results found both in ethanol dehydration and nicosulfuron removal were for the same sample of KPW supported at zeolite ZSM-5 (SiO2/Al2O3 = 30). The prominent ethanol conversion of 98% and the highest and most stable selectivity toward ethene were evidenced, along with the capacity of 28.4 mg of targeted pesticide retained per gram of designed KPW/ZSM composite. This comprehensive investigation enabled insight into active site formations in the efficient KPW/ZSM composites. Different approaches to implementation revealed that a lower Si/Al ratio in zeolite promotes efficient K+ exchange, which combined with two-phased in situ preparation of KPW as active phase, evidently leads to the formation of isolated sites of superior activity for both catalytic and adsorptive procedures.
PB  - Elsevier B.V.
T2  - Microporous and Mesoporous Materials
T1  - The environmental impact of potassium tungstophosphate/ZSM-5 zeolite: Insight into catalysis and adsorption processes
VL  - 315
DO  - 10.1016/j.micromeso.2021.110925
ER  - 

@article{
author = "Jevremović, Anka and Nedić-Vasiljević, Bojana and Popa, Alexandru and Uskoković-Marković, Snežana and Ignjatović, Ljubiša and Bajuk-Bogdanović, Danica and Milojević-Rakić, Maja",
year = "2021",
abstract = "Environmental implementation of novel composite materials comprising potassium tungstophosphate (KPW) and ZSM-5 zeolite was tested in ethene production and pesticide removal. The study revealed that the binding of KPW to ZSM-5 zeolites of different Si/Al ratios affects the formation of active centres for catalytic and adsorption processes. Brønsted active sites present in the zeolite framework are synergistically joined with Lewis centres and additional Brønsted centres through the impregnation of potassium tungstophosphate, which resulted in improvement of stability and activity of investigated materials. Adsorption and catalytic performance were found to be influenced by the order of addition of salt precursors and by post-synthesis thermal treatment. The best results found both in ethanol dehydration and nicosulfuron removal were for the same sample of KPW supported at zeolite ZSM-5 (SiO2/Al2O3 = 30). The prominent ethanol conversion of 98% and the highest and most stable selectivity toward ethene were evidenced, along with the capacity of 28.4 mg of targeted pesticide retained per gram of designed KPW/ZSM composite. This comprehensive investigation enabled insight into active site formations in the efficient KPW/ZSM composites. Different approaches to implementation revealed that a lower Si/Al ratio in zeolite promotes efficient K+ exchange, which combined with two-phased in situ preparation of KPW as active phase, evidently leads to the formation of isolated sites of superior activity for both catalytic and adsorptive procedures.",
publisher = "Elsevier B.V.",
journal = "Microporous and Mesoporous Materials",
title = "The environmental impact of potassium tungstophosphate/ZSM-5 zeolite: Insight into catalysis and adsorption processes",
volume = "315",
doi = "10.1016/j.micromeso.2021.110925"
}

Jevremović, A., Nedić-Vasiljević, B., Popa, A., Uskoković-Marković, S., Ignjatović, L., Bajuk-Bogdanović, D.,& Milojević-Rakić, M.. (2021). The environmental impact of potassium tungstophosphate/ZSM-5 zeolite: Insight into catalysis and adsorption processes. in Microporous and Mesoporous Materials
Elsevier B.V.., 315.
https://doi.org/10.1016/j.micromeso.2021.110925

Jevremović A, Nedić-Vasiljević B, Popa A, Uskoković-Marković S, Ignjatović L, Bajuk-Bogdanović D, Milojević-Rakić M. The environmental impact of potassium tungstophosphate/ZSM-5 zeolite: Insight into catalysis and adsorption processes. in Microporous and Mesoporous Materials. 2021;315.
doi:10.1016/j.micromeso.2021.110925 .

Jevremović, Anka, Nedić-Vasiljević, Bojana, Popa, Alexandru, Uskoković-Marković, Snežana, Ignjatović, Ljubiša, Bajuk-Bogdanović, Danica, Milojević-Rakić, Maja, "The environmental impact of potassium tungstophosphate/ZSM-5 zeolite: Insight into catalysis and adsorption processes" in Microporous and Mesoporous Materials, 315 (2021),
https://doi.org/10.1016/j.micromeso.2021.110925 . .

TY  - JOUR
AU  - Janićijević, Dejana
AU  - Uskoković-Marković, Snežana
AU  - Ranković, Dragan
AU  - Milenković, Marina
AU  - Jevremović, Anka
AU  - Nedić-Vasiljević, Bojana
AU  - Milojević-Rakić, Maja
AU  - Bajuk-Bogdanović, Danica
PY  - 2020
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3587
AB  - Novel composites of BEA zeolite and silver tungstophosphate were prepared by different procedures: two-step impregnation, ion-exchange, and as physical mixtures with varying component mass ratios. Composites were characterized using Atomic force microscopy, Infrared, Raman and Atomic absorption spectroscopy, and results were related to adsorption properties and antimicrobial efficiencies of the composites. Prepared samples were tested as antimicrobial agents for fungal and different bacterial strains, as well as for adsorbents for pesticide nicosulfuron in aqueous solutions by using High-performance liquid chromatography. Experimental conditions for batch adsorption testing were optimized in order to efficiently eliminate nicosulfuron from aqueous solutions, while enabling antimicrobial activity of these advanced materials. Antimicrobial efficiency of composites was verified, and indicated that silver ion persistence in the solid phase is of utmost significance for the antimicrobial activity. Spectroscopic investigation revealed interaction of the silver tungstophosphate active phase and the zeolite framework, giving evidence of uniform distribution of active sites in the synthesized materials that proved to be essential for adsorption application. The best obtained adsorption capacity, as well as highest antimicrobial efficiency, is found for composite samples prepared by two-step impregnation with (BEA: silver tungstophosphate) mass ratio 2:1. The amount of nicosulfuron removed from water suspension was 38.2 mg per gram of composite, and the minimum inhibitory concentration determined for all investigated gram-negative bacteria was 125 μg mL−1.
PB  - Elsevier
T2  - Science of the Total Environment
T1  - Double active BEA zeolite/silver tungstophosphates – Antimicrobial effects and pesticide removal
VL  - 735
DO  - 10.1016/j.scitotenv.2020.139530
ER  - 

@article{
author = "Janićijević, Dejana and Uskoković-Marković, Snežana and Ranković, Dragan and Milenković, Marina and Jevremović, Anka and Nedić-Vasiljević, Bojana and Milojević-Rakić, Maja and Bajuk-Bogdanović, Danica",
year = "2020",
abstract = "Novel composites of BEA zeolite and silver tungstophosphate were prepared by different procedures: two-step impregnation, ion-exchange, and as physical mixtures with varying component mass ratios. Composites were characterized using Atomic force microscopy, Infrared, Raman and Atomic absorption spectroscopy, and results were related to adsorption properties and antimicrobial efficiencies of the composites. Prepared samples were tested as antimicrobial agents for fungal and different bacterial strains, as well as for adsorbents for pesticide nicosulfuron in aqueous solutions by using High-performance liquid chromatography. Experimental conditions for batch adsorption testing were optimized in order to efficiently eliminate nicosulfuron from aqueous solutions, while enabling antimicrobial activity of these advanced materials. Antimicrobial efficiency of composites was verified, and indicated that silver ion persistence in the solid phase is of utmost significance for the antimicrobial activity. Spectroscopic investigation revealed interaction of the silver tungstophosphate active phase and the zeolite framework, giving evidence of uniform distribution of active sites in the synthesized materials that proved to be essential for adsorption application. The best obtained adsorption capacity, as well as highest antimicrobial efficiency, is found for composite samples prepared by two-step impregnation with (BEA: silver tungstophosphate) mass ratio 2:1. The amount of nicosulfuron removed from water suspension was 38.2 mg per gram of composite, and the minimum inhibitory concentration determined for all investigated gram-negative bacteria was 125 μg mL−1.",
publisher = "Elsevier",
journal = "Science of the Total Environment",
title = "Double active BEA zeolite/silver tungstophosphates – Antimicrobial effects and pesticide removal",
volume = "735",
doi = "10.1016/j.scitotenv.2020.139530"
}

Janićijević, D., Uskoković-Marković, S., Ranković, D., Milenković, M., Jevremović, A., Nedić-Vasiljević, B., Milojević-Rakić, M.,& Bajuk-Bogdanović, D.. (2020). Double active BEA zeolite/silver tungstophosphates – Antimicrobial effects and pesticide removal. in Science of the Total Environment
Elsevier., 735.
https://doi.org/10.1016/j.scitotenv.2020.139530

Janićijević D, Uskoković-Marković S, Ranković D, Milenković M, Jevremović A, Nedić-Vasiljević B, Milojević-Rakić M, Bajuk-Bogdanović D. Double active BEA zeolite/silver tungstophosphates – Antimicrobial effects and pesticide removal. in Science of the Total Environment. 2020;735.
doi:10.1016/j.scitotenv.2020.139530 .

Janićijević, Dejana, Uskoković-Marković, Snežana, Ranković, Dragan, Milenković, Marina, Jevremović, Anka, Nedić-Vasiljević, Bojana, Milojević-Rakić, Maja, Bajuk-Bogdanović, Danica, "Double active BEA zeolite/silver tungstophosphates – Antimicrobial effects and pesticide removal" in Science of the Total Environment, 735 (2020),
https://doi.org/10.1016/j.scitotenv.2020.139530 . .

TY  - JOUR
AU  - Jevremović, Anka
AU  - Bober, Patrycja
AU  - Mičušík, Matej
AU  - Kuliček, Jaroslav
AU  - Acharya, Udit
AU  - Pfleger, Jiří
AU  - Milojević-Rakić, Maja
AU  - Krajišnik, Danina
AU  - Trchova, Miroslava
AU  - Stejskal, Jaroslav
AU  - Ćirić-Marjanović, Gordana
PY  - 2019
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3248
AB  - Composite materials of BEA zeolite and polyaniline (PANI) were prepared by the chemical oxidative polymerization of aniline in the presence of zeolite in water (without added acid) and in an aqueous solution of sulfuric acid, using ammonium peroxydisulfate as an oxidant. Protonated (as-synthesized) and deprotonated forms of the composites and pristine PANIs were characterized by scanning electron microscopy, conductivity and zeta potential measurements, FTIR, Raman and XPS spectroscopies, and thermogravimetric analysis. Adsorption properties of synthesized materials for removal of nicosulfuron pesticide from aqueous solutions were studied, using HPLC technique. The obtained adsorption isotherms were analyzed using Freundlich and Langmuir-Freundlich equations. Protonated PANI/BEA composites showed excellent adsorption capacity (18.4–25.4 mg g−1), that was higher than the adsorption capacity of pristine BEA zeolite (18.2 mg g−1) but slightly less than neat PANI. Among PANIs, the highest adsorption capacity of 29.8 mg g−1 of adsorbent was found for protonated PANI prepared in sulfuric acid solution. Analysis of adsorption isotherms revealed high degree of surface homogeneity for all prepared composite materials and PANIs. Proposed mechanism for enhanced adsorption of nicosulfuron on protonated composites is based on hydrogen bonding of nicosulfuron O- and N-containing groups with bridging hydroxyls of BEA zeolite and –NH/ = NH+/−NH•+ groups in protonated emeraldine salt form of PANI chains (PANI-ES), accompanied with electrostatic attractive interaction between anionic nicosulfuron species and positive = NH+/−NH•+ groups in bipolaron/polaron containing structures of PANI-ES. Presence of protons in bridging hydroxyls in BEA zeolite and in protonated PANI-ES chains is essential for excellent adsorption of nicosulfuron via hydrogen bonding on all protonated composite samples. In support of this interpretation, deprotonated PANI/BEA composites and deprotonated PANIs showed significantly lower adsorption capacities (in the range 5.5–13.0 mg g−1) compared to those of their protonated counterparts.
PB  - Elsevier B.V.
T2  - Microporous and Mesoporous Materials
T1  - Synthesis and characterization of polyaniline/BEA zeolite composites and their application in nicosulfuron adsorption
SP  - 234
EP  - 245
DO  - 10.1016/j.micromeso.2019.06.006
ER  - 

@article{
author = "Jevremović, Anka and Bober, Patrycja and Mičušík, Matej and Kuliček, Jaroslav and Acharya, Udit and Pfleger, Jiří and Milojević-Rakić, Maja and Krajišnik, Danina and Trchova, Miroslava and Stejskal, Jaroslav and Ćirić-Marjanović, Gordana",
year = "2019",
abstract = "Composite materials of BEA zeolite and polyaniline (PANI) were prepared by the chemical oxidative polymerization of aniline in the presence of zeolite in water (without added acid) and in an aqueous solution of sulfuric acid, using ammonium peroxydisulfate as an oxidant. Protonated (as-synthesized) and deprotonated forms of the composites and pristine PANIs were characterized by scanning electron microscopy, conductivity and zeta potential measurements, FTIR, Raman and XPS spectroscopies, and thermogravimetric analysis. Adsorption properties of synthesized materials for removal of nicosulfuron pesticide from aqueous solutions were studied, using HPLC technique. The obtained adsorption isotherms were analyzed using Freundlich and Langmuir-Freundlich equations. Protonated PANI/BEA composites showed excellent adsorption capacity (18.4–25.4 mg g−1), that was higher than the adsorption capacity of pristine BEA zeolite (18.2 mg g−1) but slightly less than neat PANI. Among PANIs, the highest adsorption capacity of 29.8 mg g−1 of adsorbent was found for protonated PANI prepared in sulfuric acid solution. Analysis of adsorption isotherms revealed high degree of surface homogeneity for all prepared composite materials and PANIs. Proposed mechanism for enhanced adsorption of nicosulfuron on protonated composites is based on hydrogen bonding of nicosulfuron O- and N-containing groups with bridging hydroxyls of BEA zeolite and –NH/ = NH+/−NH•+ groups in protonated emeraldine salt form of PANI chains (PANI-ES), accompanied with electrostatic attractive interaction between anionic nicosulfuron species and positive = NH+/−NH•+ groups in bipolaron/polaron containing structures of PANI-ES. Presence of protons in bridging hydroxyls in BEA zeolite and in protonated PANI-ES chains is essential for excellent adsorption of nicosulfuron via hydrogen bonding on all protonated composite samples. In support of this interpretation, deprotonated PANI/BEA composites and deprotonated PANIs showed significantly lower adsorption capacities (in the range 5.5–13.0 mg g−1) compared to those of their protonated counterparts.",
publisher = "Elsevier B.V.",
journal = "Microporous and Mesoporous Materials",
title = "Synthesis and characterization of polyaniline/BEA zeolite composites and their application in nicosulfuron adsorption",
pages = "234-245",
doi = "10.1016/j.micromeso.2019.06.006"
}

Jevremović, A., Bober, P., Mičušík, M., Kuliček, J., Acharya, U., Pfleger, J., Milojević-Rakić, M., Krajišnik, D., Trchova, M., Stejskal, J.,& Ćirić-Marjanović, G.. (2019). Synthesis and characterization of polyaniline/BEA zeolite composites and their application in nicosulfuron adsorption. in Microporous and Mesoporous Materials
Elsevier B.V.., 234-245.
https://doi.org/10.1016/j.micromeso.2019.06.006

Jevremović A, Bober P, Mičušík M, Kuliček J, Acharya U, Pfleger J, Milojević-Rakić M, Krajišnik D, Trchova M, Stejskal J, Ćirić-Marjanović G. Synthesis and characterization of polyaniline/BEA zeolite composites and their application in nicosulfuron adsorption. in Microporous and Mesoporous Materials. 2019;:234-245.
doi:10.1016/j.micromeso.2019.06.006 .

Jevremović, Anka, Bober, Patrycja, Mičušík, Matej, Kuliček, Jaroslav, Acharya, Udit, Pfleger, Jiří, Milojević-Rakić, Maja, Krajišnik, Danina, Trchova, Miroslava, Stejskal, Jaroslav, Ćirić-Marjanović, Gordana, "Synthesis and characterization of polyaniline/BEA zeolite composites and their application in nicosulfuron adsorption" in Microporous and Mesoporous Materials (2019):234-245,
https://doi.org/10.1016/j.micromeso.2019.06.006 . .

TY  - JOUR
AU  - Holclajtner-Antunović, Ivanka
AU  - Uskoković-Marković, Snežana
AU  - Popa, Alexandru
AU  - Jevremović, A
AU  - Nedić-Vasiljević, Bojana
AU  - Milojević-Rakić, Maja
AU  - Bajuk-Bogdanović, Danica
PY  - 2019
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3280
AB  - The current study reports the synthesis, characterization and catalytic activity of tungstophosphoric acid (HPW) and its potassium salts (KH2PW and K3PW) supported on activated carbon (AC). Because potassium salts of tungstophosphoric acid are insoluble, the carbon supported KH2PW and K3PW were prepared by a two step impregnation method. The synthesized catalysts were characterized by various physicochemical methods such as Fourier transform infrared and Raman spectroscopy, differential thermal analysis, thermogravimetric analysis, X-ray diffraction, scanning electron microscopy and nitrogen physisorption. It is observed that all active phases keep their Keggin-type structure after being supported on AC, while their specific surface area is considerably increased by deposition on this porous substrate. The results also indicated that the synthesized materials retained the morphology specific for the support as well as its thermal properties. The adsorption behaviour of the nanocomposites towards nicosulfuron pesticide was found to be particulary good and even slightly improved when compared to pure activated carbon. The catalytic activity of the prepared catalysts was probed for the vapor phase dehydration of ethanol at 300 °C. The conversion of ethanol and selectivity toward ethylene and diethyl ether of nanocomposites were compared with the values of bare HPW, KH2PW and K3PW. Results revealed that catalytic activity depends on the catalyst type and active phase loading. The conversion over unsupported catalysts decreased by increasing the cation content per Keggin unit. The nanocomposites with 30 wt% loading of HPW achieved the best conversion of nearly 100% and the highest and stable selectivity toward ethylene. The catalytic activity of nanocomposites with acidic KH2PW showed lower catalytic activity of about 70%, while the nanocomposites of neutral K3PW and AC showed negligible activity.
PB  - Springer Netherlands
T2  - Records of Natural Products
T1  - Ethanol dehydration over Keggin type tungstophosphoric acid and its potassium salts supported on carbon
DO  - 10.1007/s11144-019-01625-6
ER  - 

@article{
author = "Holclajtner-Antunović, Ivanka and Uskoković-Marković, Snežana and Popa, Alexandru and Jevremović, A and Nedić-Vasiljević, Bojana and Milojević-Rakić, Maja and Bajuk-Bogdanović, Danica",
year = "2019",
abstract = "The current study reports the synthesis, characterization and catalytic activity of tungstophosphoric acid (HPW) and its potassium salts (KH2PW and K3PW) supported on activated carbon (AC). Because potassium salts of tungstophosphoric acid are insoluble, the carbon supported KH2PW and K3PW were prepared by a two step impregnation method. The synthesized catalysts were characterized by various physicochemical methods such as Fourier transform infrared and Raman spectroscopy, differential thermal analysis, thermogravimetric analysis, X-ray diffraction, scanning electron microscopy and nitrogen physisorption. It is observed that all active phases keep their Keggin-type structure after being supported on AC, while their specific surface area is considerably increased by deposition on this porous substrate. The results also indicated that the synthesized materials retained the morphology specific for the support as well as its thermal properties. The adsorption behaviour of the nanocomposites towards nicosulfuron pesticide was found to be particulary good and even slightly improved when compared to pure activated carbon. The catalytic activity of the prepared catalysts was probed for the vapor phase dehydration of ethanol at 300 °C. The conversion of ethanol and selectivity toward ethylene and diethyl ether of nanocomposites were compared with the values of bare HPW, KH2PW and K3PW. Results revealed that catalytic activity depends on the catalyst type and active phase loading. The conversion over unsupported catalysts decreased by increasing the cation content per Keggin unit. The nanocomposites with 30 wt% loading of HPW achieved the best conversion of nearly 100% and the highest and stable selectivity toward ethylene. The catalytic activity of nanocomposites with acidic KH2PW showed lower catalytic activity of about 70%, while the nanocomposites of neutral K3PW and AC showed negligible activity.",
publisher = "Springer Netherlands",
journal = "Records of Natural Products",
title = "Ethanol dehydration over Keggin type tungstophosphoric acid and its potassium salts supported on carbon",
doi = "10.1007/s11144-019-01625-6"
}

Holclajtner-Antunović, I., Uskoković-Marković, S., Popa, A., Jevremović, A., Nedić-Vasiljević, B., Milojević-Rakić, M.,& Bajuk-Bogdanović, D.. (2019). Ethanol dehydration over Keggin type tungstophosphoric acid and its potassium salts supported on carbon. in Records of Natural Products
Springer Netherlands..
https://doi.org/10.1007/s11144-019-01625-6

Holclajtner-Antunović I, Uskoković-Marković S, Popa A, Jevremović A, Nedić-Vasiljević B, Milojević-Rakić M, Bajuk-Bogdanović D. Ethanol dehydration over Keggin type tungstophosphoric acid and its potassium salts supported on carbon. in Records of Natural Products. 2019;.
doi:10.1007/s11144-019-01625-6 .

Holclajtner-Antunović, Ivanka, Uskoković-Marković, Snežana, Popa, Alexandru, Jevremović, A, Nedić-Vasiljević, Bojana, Milojević-Rakić, Maja, Bajuk-Bogdanović, Danica, "Ethanol dehydration over Keggin type tungstophosphoric acid and its potassium salts supported on carbon" in Records of Natural Products (2019),
https://doi.org/10.1007/s11144-019-01625-6 . .

TY  - JOUR
AU  - Ćirić-Marjanović, Gordana
AU  - Milojević-Rakić, Maja
AU  - Janošević-Ležaić, Aleksandra
AU  - Luginbuhl, Sandra
AU  - Walde, Peter
PY  - 2017
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/2938
AB  - The literature concerning the oxidative oligomerization and polymerization of various arylamines, e.g., aniline, substituted anilines, aminonaphthalene and its derivatives, catalyzed by oxidoreductases, such as laccases and peroxidases, in aqueous, organic, and mixed aqueous organic monophasic or biphasic media, is reviewed. An overview of template-free as well as template-assisted enzymatic syntheses of oligomers and polymers of arylamines is given. Special attention is paid to mechanistic aspects of these biocatalytic processes. Because of the nontoxicity of oxidoreductases and their high catalytic efficiency, as well as high selectivity of enzymatic oligomerizations/polymerizations under mild conditions-using mainly water as a solvent and often resulting in minimal byproduct formation-enzymatic oligomerizations and polymerizations of arylamines are environmentally friendly and significantly contribute to a "green'' chemistry of conducting and redox-active oligomers and polymers. Current and potential future applications of enzymatic polymerization processes and enzymatically synthesized oligo/polyarylamines are discussed.
PB  - Springer International Publishing Ag, Cham
T2  - Chemical Papers
T1  - Enzymatic oligomerization and polymerization of arylamines: state of the art and perspectives
VL  - 71
IS  - 2
SP  - 199
EP  - 242
DO  - 10.1007/s11696-016-0094-3
ER  - 

@article{
author = "Ćirić-Marjanović, Gordana and Milojević-Rakić, Maja and Janošević-Ležaić, Aleksandra and Luginbuhl, Sandra and Walde, Peter",
year = "2017",
abstract = "The literature concerning the oxidative oligomerization and polymerization of various arylamines, e.g., aniline, substituted anilines, aminonaphthalene and its derivatives, catalyzed by oxidoreductases, such as laccases and peroxidases, in aqueous, organic, and mixed aqueous organic monophasic or biphasic media, is reviewed. An overview of template-free as well as template-assisted enzymatic syntheses of oligomers and polymers of arylamines is given. Special attention is paid to mechanistic aspects of these biocatalytic processes. Because of the nontoxicity of oxidoreductases and their high catalytic efficiency, as well as high selectivity of enzymatic oligomerizations/polymerizations under mild conditions-using mainly water as a solvent and often resulting in minimal byproduct formation-enzymatic oligomerizations and polymerizations of arylamines are environmentally friendly and significantly contribute to a "green'' chemistry of conducting and redox-active oligomers and polymers. Current and potential future applications of enzymatic polymerization processes and enzymatically synthesized oligo/polyarylamines are discussed.",
publisher = "Springer International Publishing Ag, Cham",
journal = "Chemical Papers",
title = "Enzymatic oligomerization and polymerization of arylamines: state of the art and perspectives",
volume = "71",
number = "2",
pages = "199-242",
doi = "10.1007/s11696-016-0094-3"
}

Ćirić-Marjanović, G., Milojević-Rakić, M., Janošević-Ležaić, A., Luginbuhl, S.,& Walde, P.. (2017). Enzymatic oligomerization and polymerization of arylamines: state of the art and perspectives. in Chemical Papers
Springer International Publishing Ag, Cham., 71(2), 199-242.
https://doi.org/10.1007/s11696-016-0094-3

Ćirić-Marjanović G, Milojević-Rakić M, Janošević-Ležaić A, Luginbuhl S, Walde P. Enzymatic oligomerization and polymerization of arylamines: state of the art and perspectives. in Chemical Papers. 2017;71(2):199-242.
doi:10.1007/s11696-016-0094-3 .

Ćirić-Marjanović, Gordana, Milojević-Rakić, Maja, Janošević-Ležaić, Aleksandra, Luginbuhl, Sandra, Walde, Peter, "Enzymatic oligomerization and polymerization of arylamines: state of the art and perspectives" in Chemical Papers, 71, no. 2 (2017):199-242,
https://doi.org/10.1007/s11696-016-0094-3 . .

TY  - JOUR
AU  - Ćirić-Marjanović, Gordana
AU  - Milojević-Rakić, Maja
AU  - Janošević-Ležaić, Aleksandra
AU  - Luginbuhl, Sandra
AU  - Walde, Peter
PY  - 2017
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/2820
PB  - Springer International Publishing Ag, Cham
T2  - Chemical Papers
T1  - Enzymatic oligomerization and polymerization of arylamines: state of the art and perspectives (vol 71, pg 199, 2017)
VL  - 71
IS  - 9
SP  - 1797
EP  - 1797
DO  - 10.1007/s11696-017-0247-z
ER  - 

@article{
author = "Ćirić-Marjanović, Gordana and Milojević-Rakić, Maja and Janošević-Ležaić, Aleksandra and Luginbuhl, Sandra and Walde, Peter",
year = "2017",
publisher = "Springer International Publishing Ag, Cham",
journal = "Chemical Papers",
title = "Enzymatic oligomerization and polymerization of arylamines: state of the art and perspectives (vol 71, pg 199, 2017)",
volume = "71",
number = "9",
pages = "1797-1797",
doi = "10.1007/s11696-017-0247-z"
}

Ćirić-Marjanović, G., Milojević-Rakić, M., Janošević-Ležaić, A., Luginbuhl, S.,& Walde, P.. (2017). Enzymatic oligomerization and polymerization of arylamines: state of the art and perspectives (vol 71, pg 199, 2017). in Chemical Papers
Springer International Publishing Ag, Cham., 71(9), 1797-1797.
https://doi.org/10.1007/s11696-017-0247-z

Ćirić-Marjanović G, Milojević-Rakić M, Janošević-Ležaić A, Luginbuhl S, Walde P. Enzymatic oligomerization and polymerization of arylamines: state of the art and perspectives (vol 71, pg 199, 2017). in Chemical Papers. 2017;71(9):1797-1797.
doi:10.1007/s11696-017-0247-z .

Ćirić-Marjanović, Gordana, Milojević-Rakić, Maja, Janošević-Ležaić, Aleksandra, Luginbuhl, Sandra, Walde, Peter, "Enzymatic oligomerization and polymerization of arylamines: state of the art and perspectives (vol 71, pg 199, 2017)" in Chemical Papers, 71, no. 9 (2017):1797-1797,
https://doi.org/10.1007/s11696-017-0247-z . .

TY  - JOUR
AU  - Jović, A.
AU  - Bajuk-Bogdanović, Danica
AU  - Nedić-Vasiljević, Bojana
AU  - Milojević-Rakić, Maja
AU  - Krajišnik, Danina
AU  - Dondur, Vera
AU  - Popa, Alexandru
AU  - Uskoković-Marković, Snežana
AU  - Holclajtner-Antunović, Ivanka
PY  - 2017
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/2932
AB  - An optimized synthetic route for obtaining heteropoly acid (HPA) species supported on BEA zeolite was applied, and different samples, comprising 20 to 50 wt% of 12-phosphotungstic acid (HPW) were prepared. The as-synthesized supported HPW were subjected to different post-synthesis routes, which involved calcination and ultrasound treatment. Characterization of these materials was performed by means of Scanning Electron Microscopy, zeta potential measurements, Infrared Spectroscopy and X-ray Powder Diffraction analysis. Results suggest strong interaction of HPW with the support and revealed that ultrasound treatment resulted in better dispersion of active phase and thus homogeneous morphology of the samples. The zeta potential was found to be dependent on the preparation procedure and HPW content in these materials, while higher HPW loadings induced its agglomeration. Catalytic activity of the synthesized materials was investigated in an ethanol dehydration reaction, where lower HPW loadings induced higher ethanol conversion. Acid sites distribution and accessibility for ethanol molecules were found to be more essential for catalytic activity than HPW loadings, i.e., amount of active sites present in these hybrid materials.
PB  - Elsevier Science Sa, Lausanne
T2  - Materials Chemistry and Physics
T1  - Synthesis and characterization of 12-phosphotungstic acid supported on BEA zeolite
VL  - 186
SP  - 430
EP  - 437
DO  - 10.1016/j.matchemphys.2016.11.015
ER  - 

@article{
author = "Jović, A. and Bajuk-Bogdanović, Danica and Nedić-Vasiljević, Bojana and Milojević-Rakić, Maja and Krajišnik, Danina and Dondur, Vera and Popa, Alexandru and Uskoković-Marković, Snežana and Holclajtner-Antunović, Ivanka",
year = "2017",
abstract = "An optimized synthetic route for obtaining heteropoly acid (HPA) species supported on BEA zeolite was applied, and different samples, comprising 20 to 50 wt% of 12-phosphotungstic acid (HPW) were prepared. The as-synthesized supported HPW were subjected to different post-synthesis routes, which involved calcination and ultrasound treatment. Characterization of these materials was performed by means of Scanning Electron Microscopy, zeta potential measurements, Infrared Spectroscopy and X-ray Powder Diffraction analysis. Results suggest strong interaction of HPW with the support and revealed that ultrasound treatment resulted in better dispersion of active phase and thus homogeneous morphology of the samples. The zeta potential was found to be dependent on the preparation procedure and HPW content in these materials, while higher HPW loadings induced its agglomeration. Catalytic activity of the synthesized materials was investigated in an ethanol dehydration reaction, where lower HPW loadings induced higher ethanol conversion. Acid sites distribution and accessibility for ethanol molecules were found to be more essential for catalytic activity than HPW loadings, i.e., amount of active sites present in these hybrid materials.",
publisher = "Elsevier Science Sa, Lausanne",
journal = "Materials Chemistry and Physics",
title = "Synthesis and characterization of 12-phosphotungstic acid supported on BEA zeolite",
volume = "186",
pages = "430-437",
doi = "10.1016/j.matchemphys.2016.11.015"
}

Jović, A., Bajuk-Bogdanović, D., Nedić-Vasiljević, B., Milojević-Rakić, M., Krajišnik, D., Dondur, V., Popa, A., Uskoković-Marković, S.,& Holclajtner-Antunović, I.. (2017). Synthesis and characterization of 12-phosphotungstic acid supported on BEA zeolite. in Materials Chemistry and Physics
Elsevier Science Sa, Lausanne., 186, 430-437.
https://doi.org/10.1016/j.matchemphys.2016.11.015

Jović A, Bajuk-Bogdanović D, Nedić-Vasiljević B, Milojević-Rakić M, Krajišnik D, Dondur V, Popa A, Uskoković-Marković S, Holclajtner-Antunović I. Synthesis and characterization of 12-phosphotungstic acid supported on BEA zeolite. in Materials Chemistry and Physics. 2017;186:430-437.
doi:10.1016/j.matchemphys.2016.11.015 .

Jović, A., Bajuk-Bogdanović, Danica, Nedić-Vasiljević, Bojana, Milojević-Rakić, Maja, Krajišnik, Danina, Dondur, Vera, Popa, Alexandru, Uskoković-Marković, Snežana, Holclajtner-Antunović, Ivanka, "Synthesis and characterization of 12-phosphotungstic acid supported on BEA zeolite" in Materials Chemistry and Physics, 186 (2017):430-437,
https://doi.org/10.1016/j.matchemphys.2016.11.015 . .

TY  - JOUR
AU  - Bajuk-Bogdanović, Danica
AU  - Jović, Aleksandar
AU  - Nedić-Vasiljević, Bojana
AU  - Milojević-Rakić, Maja
AU  - Kragović, Milan
AU  - Krajišnik, Danina
AU  - Holclajtner-Antunović, Ivanka
AU  - Dondur, Vera
PY  - 2017
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/2873
AB  - Tungstophosphoric acid and BEA zeolite composites were synthesized by wetness impregnation, followed by ultrasonication and calcination. Composites were characterized using Raman spectroscopy, thermal analysis and pH-dependent zeta potential. Spectroscopic measurements indicated the interaction of acid and the support by binding of polyanion terminal oxygens and BEA extra framework H+ via hydrogen bonds. Evaluation of prepared composites revealed their higher efficiency in nicosulfuron adsorption, in comparison to parent zeolite. All prepared composites showed excellent adsorption properties for pesticide removal in the range 12.1-25.8 mg of nicosulfuron per gram of investigated sample. Better adsorption capacity was found for sonicated samples in comparison to as-synthesized and calcined ones. It was found that the amount of polyanion in the composites and the extent of the particles surface charge are not crucial for the adsorption application, it is rather the uniformity of the zeolite surface coverage with the polyanion that is was more important.
PB  - Elsevier Science BV, Amsterdam
T2  - Materials Science and Engineering B: Advanced Functional Solid-State Materials
T1  - 12-Tungstophosphoric acid/BEA zeolite composites - Characterization and application for pesticide removal
VL  - 225
SP  - 60
EP  - 67
DO  - 10.1016/j.mseb.2017.08.011
ER  - 

@article{
author = "Bajuk-Bogdanović, Danica and Jović, Aleksandar and Nedić-Vasiljević, Bojana and Milojević-Rakić, Maja and Kragović, Milan and Krajišnik, Danina and Holclajtner-Antunović, Ivanka and Dondur, Vera",
year = "2017",
abstract = "Tungstophosphoric acid and BEA zeolite composites were synthesized by wetness impregnation, followed by ultrasonication and calcination. Composites were characterized using Raman spectroscopy, thermal analysis and pH-dependent zeta potential. Spectroscopic measurements indicated the interaction of acid and the support by binding of polyanion terminal oxygens and BEA extra framework H+ via hydrogen bonds. Evaluation of prepared composites revealed their higher efficiency in nicosulfuron adsorption, in comparison to parent zeolite. All prepared composites showed excellent adsorption properties for pesticide removal in the range 12.1-25.8 mg of nicosulfuron per gram of investigated sample. Better adsorption capacity was found for sonicated samples in comparison to as-synthesized and calcined ones. It was found that the amount of polyanion in the composites and the extent of the particles surface charge are not crucial for the adsorption application, it is rather the uniformity of the zeolite surface coverage with the polyanion that is was more important.",
publisher = "Elsevier Science BV, Amsterdam",
journal = "Materials Science and Engineering B: Advanced Functional Solid-State Materials",
title = "12-Tungstophosphoric acid/BEA zeolite composites - Characterization and application for pesticide removal",
volume = "225",
pages = "60-67",
doi = "10.1016/j.mseb.2017.08.011"
}

Bajuk-Bogdanović, D., Jović, A., Nedić-Vasiljević, B., Milojević-Rakić, M., Kragović, M., Krajišnik, D., Holclajtner-Antunović, I.,& Dondur, V.. (2017). 12-Tungstophosphoric acid/BEA zeolite composites - Characterization and application for pesticide removal. in Materials Science and Engineering B: Advanced Functional Solid-State Materials
Elsevier Science BV, Amsterdam., 225, 60-67.
https://doi.org/10.1016/j.mseb.2017.08.011

Bajuk-Bogdanović D, Jović A, Nedić-Vasiljević B, Milojević-Rakić M, Kragović M, Krajišnik D, Holclajtner-Antunović I, Dondur V. 12-Tungstophosphoric acid/BEA zeolite composites - Characterization and application for pesticide removal. in Materials Science and Engineering B: Advanced Functional Solid-State Materials. 2017;225:60-67.
doi:10.1016/j.mseb.2017.08.011 .

Bajuk-Bogdanović, Danica, Jović, Aleksandar, Nedić-Vasiljević, Bojana, Milojević-Rakić, Maja, Kragović, Milan, Krajišnik, Danina, Holclajtner-Antunović, Ivanka, Dondur, Vera, "12-Tungstophosphoric acid/BEA zeolite composites - Characterization and application for pesticide removal" in Materials Science and Engineering B: Advanced Functional Solid-State Materials, 225 (2017):60-67,
https://doi.org/10.1016/j.mseb.2017.08.011 . .

TY  - JOUR
AU  - Krajišnik, Danina
AU  - Daković, Aleksandra
AU  - Malenović, Anđelija
AU  - Milojević-Rakić, Maja
AU  - Dondur, Vera
AU  - Radulović, Željka
AU  - Milić, Jela
PY  - 2013
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/1905
AB  - Results on adsorption of diclofenac sodium (DS) by modified natural zeolite composites at three levels (10,20 and 30 mmol/100 g) of cationic surfactant-hexadecyltrimethylammonium bromide (HB), in a buffer solution, were compared. Characterization of composites before and after drug adsorption was performed by determination of electrokinetic mobility, FTIR and thermal analysis. The results indicated interactions between drug and carriers. The pharmaceutical performance of cationic surfactant-modified zeolites as drug formulation excipients was evaluated by in vitro dissolution experiments. The results were compared with the drug release from corresponding physical mixtures. Prolonged drug release over a period of 8 h (up to 30%) was achieved with both groups of samples. Furthermore, DS release reached up to 85% from physical mixtures containing drug amount closer to a therapeutic dose.
PB  - Elsevier Science BV, Amsterdam
T2  - Applied Clay Science
T1  - Investigation of adsorption and release of diclofenac sodium by modified zeolites composites
SP  - 322
EP  - 326
DO  - 10.1016/j.clay.2013.08.011
ER  - 

@article{
author = "Krajišnik, Danina and Daković, Aleksandra and Malenović, Anđelija and Milojević-Rakić, Maja and Dondur, Vera and Radulović, Željka and Milić, Jela",
year = "2013",
abstract = "Results on adsorption of diclofenac sodium (DS) by modified natural zeolite composites at three levels (10,20 and 30 mmol/100 g) of cationic surfactant-hexadecyltrimethylammonium bromide (HB), in a buffer solution, were compared. Characterization of composites before and after drug adsorption was performed by determination of electrokinetic mobility, FTIR and thermal analysis. The results indicated interactions between drug and carriers. The pharmaceutical performance of cationic surfactant-modified zeolites as drug formulation excipients was evaluated by in vitro dissolution experiments. The results were compared with the drug release from corresponding physical mixtures. Prolonged drug release over a period of 8 h (up to 30%) was achieved with both groups of samples. Furthermore, DS release reached up to 85% from physical mixtures containing drug amount closer to a therapeutic dose.",
publisher = "Elsevier Science BV, Amsterdam",
journal = "Applied Clay Science",
title = "Investigation of adsorption and release of diclofenac sodium by modified zeolites composites",
pages = "322-326",
doi = "10.1016/j.clay.2013.08.011"
}

Krajišnik, D., Daković, A., Malenović, A., Milojević-Rakić, M., Dondur, V., Radulović, Ž.,& Milić, J.. (2013). Investigation of adsorption and release of diclofenac sodium by modified zeolites composites. in Applied Clay Science
Elsevier Science BV, Amsterdam., 322-326.
https://doi.org/10.1016/j.clay.2013.08.011

Krajišnik D, Daković A, Malenović A, Milojević-Rakić M, Dondur V, Radulović Ž, Milić J. Investigation of adsorption and release of diclofenac sodium by modified zeolites composites. in Applied Clay Science. 2013;:322-326.
doi:10.1016/j.clay.2013.08.011 .

Krajišnik, Danina, Daković, Aleksandra, Malenović, Anđelija, Milojević-Rakić, Maja, Dondur, Vera, Radulović, Željka, Milić, Jela, "Investigation of adsorption and release of diclofenac sodium by modified zeolites composites" in Applied Clay Science (2013):322-326,
https://doi.org/10.1016/j.clay.2013.08.011 . .

TY  - JOUR
AU  - Milojević-Rakić, Maja
AU  - Janošević, Aleksandra
AU  - Krstić, Jugoslav
AU  - Nedić-Vasiljević, Bojana
AU  - Dondur, Vera
AU  - Ćirić-Marjanović, Gordana
PY  - 2013
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/1867
AB  - Nanostructured and granular polyanilines (PANIs) and their composites with zeolite ZSM-5, synthesized by the oxidative polymerization of aniline in water and aqueous solution of sulfuric acid, are evaluated as adsorbents of the organic herbicide glyphosate [N-(phosphonomethyl)glycine] in aqueous solution. The protonated and deprotonated forms of synthesized materials were characterized by elemental and thermogravimetric analysis, scanning electron microscopy, FTIR, Raman and UV-Vis spectroscopies, X-ray powder diffraction, and nitrogen physisorption measurements. The adsorption isotherms of glyphosate on studied materials were best fitted by Freundlich and Langmuir-Freundlich models. The adsorption characteristics of the investigated PANIs and PANI/ZSM-5 composites were found to be much more influenced by the oxidation state and protonation level of PANI in the adsorbents then by the textural and morphological properties of materials. The highest adsorption of glyphosate among all investigated PANI and PANI/ZSM-5 samples, as well as pure ZSM-5, exhibited the deprotonated granular PANI which was synthesized in sulfuric acid medium (98.5 mg/g). High adsorption capacity also showed the deprotonated PANI/ZSM-5 composite with similar to 50% of zeolite (61.9 mg/g) and the protonated nanostructured PANI (59.9 mg/g), both materials prepared in water without added acid.
PB  - Elsevier Science BV, Amsterdam
T2  - Microporous and Mesoporous Materials
T1  - Polyaniline and its composites with zeolite ZSM-5 for efficient removal of glyphosate from aqueous solution
VL  - 180
SP  - 141
EP  - 155
DO  - 10.1016/j.micromeso.2013.06.025
ER  - 

@article{
author = "Milojević-Rakić, Maja and Janošević, Aleksandra and Krstić, Jugoslav and Nedić-Vasiljević, Bojana and Dondur, Vera and Ćirić-Marjanović, Gordana",
year = "2013",
abstract = "Nanostructured and granular polyanilines (PANIs) and their composites with zeolite ZSM-5, synthesized by the oxidative polymerization of aniline in water and aqueous solution of sulfuric acid, are evaluated as adsorbents of the organic herbicide glyphosate [N-(phosphonomethyl)glycine] in aqueous solution. The protonated and deprotonated forms of synthesized materials were characterized by elemental and thermogravimetric analysis, scanning electron microscopy, FTIR, Raman and UV-Vis spectroscopies, X-ray powder diffraction, and nitrogen physisorption measurements. The adsorption isotherms of glyphosate on studied materials were best fitted by Freundlich and Langmuir-Freundlich models. The adsorption characteristics of the investigated PANIs and PANI/ZSM-5 composites were found to be much more influenced by the oxidation state and protonation level of PANI in the adsorbents then by the textural and morphological properties of materials. The highest adsorption of glyphosate among all investigated PANI and PANI/ZSM-5 samples, as well as pure ZSM-5, exhibited the deprotonated granular PANI which was synthesized in sulfuric acid medium (98.5 mg/g). High adsorption capacity also showed the deprotonated PANI/ZSM-5 composite with similar to 50% of zeolite (61.9 mg/g) and the protonated nanostructured PANI (59.9 mg/g), both materials prepared in water without added acid.",
publisher = "Elsevier Science BV, Amsterdam",
journal = "Microporous and Mesoporous Materials",
title = "Polyaniline and its composites with zeolite ZSM-5 for efficient removal of glyphosate from aqueous solution",
volume = "180",
pages = "141-155",
doi = "10.1016/j.micromeso.2013.06.025"
}

Milojević-Rakić, M., Janošević, A., Krstić, J., Nedić-Vasiljević, B., Dondur, V.,& Ćirić-Marjanović, G.. (2013). Polyaniline and its composites with zeolite ZSM-5 for efficient removal of glyphosate from aqueous solution. in Microporous and Mesoporous Materials
Elsevier Science BV, Amsterdam., 180, 141-155.
https://doi.org/10.1016/j.micromeso.2013.06.025

Milojević-Rakić M, Janošević A, Krstić J, Nedić-Vasiljević B, Dondur V, Ćirić-Marjanović G. Polyaniline and its composites with zeolite ZSM-5 for efficient removal of glyphosate from aqueous solution. in Microporous and Mesoporous Materials. 2013;180:141-155.
doi:10.1016/j.micromeso.2013.06.025 .

Milojević-Rakić, Maja, Janošević, Aleksandra, Krstić, Jugoslav, Nedić-Vasiljević, Bojana, Dondur, Vera, Ćirić-Marjanović, Gordana, "Polyaniline and its composites with zeolite ZSM-5 for efficient removal of glyphosate from aqueous solution" in Microporous and Mesoporous Materials, 180 (2013):141-155,
https://doi.org/10.1016/j.micromeso.2013.06.025 . .

TY  - JOUR
AU  - Krajišnik, Danina
AU  - Daković, Aleksandra
AU  - Milojević, Maja
AU  - Malenović, Anđelija
AU  - Kragović, Milan
AU  - Bajuk-Bogdanović, Danica
AU  - Dondur, Vera
AU  - Milić, Jela
PY  - 2011
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/1541
AB  - In this study an investigation of a model drug sorption onto cationic surfactant-modified natural zeolites as a drug formulation excipient was performed. Natural zeolite was modified with cetylpyridinium chloride in amounts equivalent to 100, 200 and 300% of its external cation-exchange capacity. The starting material and obtained organozeolites were characterized by Fourier transform infrared spectroscopy, zeta potential measurements and thermal analysis. In vitro sorption of diclofenac sodium as a model drug was studied for all surfactant/zeolite composites by means of sorption isotherm measurements in aqueous solutions (pH 7.4). The modified zeolites with three levels of surfactant coverage within the short activation time were prepared. Zeta potential measurements and thermal analysis showed that when the surfactant loading level was equal to external cation-exchange value, almost monolayer of organic phase were present at the zeolitic surface while higher amounts of surfactant produced less extended bilayers, ordered bilayers or admicelles at the zeolitic surface. Modified zeolites, obtained in this manner, were effective in diclofenac sodium sorption and the organic phase derived from adsorbed cetylpyridinium chloride was the primary sorption phase for the model drug. The Langmuir isotherm was found to describe the equilibrium sorption data well over the entire concentration range. The separate contributions of the adsorption and partition to the total sorption of DS were analyzed mathematically. Results revealed that that adsorption and partitioning of the model drug take place simultaneously.
PB  - Elsevier Science BV, Amsterdam
T2  - Colloids and Surfaces B: Biointerfaces
T1  - Properties of diclofenac sodium sorption onto natural zeolite modified with cetylpyridinium chloride
VL  - 83
IS  - 1
SP  - 165
EP  - 172
DO  - 10.1016/j.colsurfb.2010.11.024
ER  - 

@article{
author = "Krajišnik, Danina and Daković, Aleksandra and Milojević, Maja and Malenović, Anđelija and Kragović, Milan and Bajuk-Bogdanović, Danica and Dondur, Vera and Milić, Jela",
year = "2011",
abstract = "In this study an investigation of a model drug sorption onto cationic surfactant-modified natural zeolites as a drug formulation excipient was performed. Natural zeolite was modified with cetylpyridinium chloride in amounts equivalent to 100, 200 and 300% of its external cation-exchange capacity. The starting material and obtained organozeolites were characterized by Fourier transform infrared spectroscopy, zeta potential measurements and thermal analysis. In vitro sorption of diclofenac sodium as a model drug was studied for all surfactant/zeolite composites by means of sorption isotherm measurements in aqueous solutions (pH 7.4). The modified zeolites with three levels of surfactant coverage within the short activation time were prepared. Zeta potential measurements and thermal analysis showed that when the surfactant loading level was equal to external cation-exchange value, almost monolayer of organic phase were present at the zeolitic surface while higher amounts of surfactant produced less extended bilayers, ordered bilayers or admicelles at the zeolitic surface. Modified zeolites, obtained in this manner, were effective in diclofenac sodium sorption and the organic phase derived from adsorbed cetylpyridinium chloride was the primary sorption phase for the model drug. The Langmuir isotherm was found to describe the equilibrium sorption data well over the entire concentration range. The separate contributions of the adsorption and partition to the total sorption of DS were analyzed mathematically. Results revealed that that adsorption and partitioning of the model drug take place simultaneously.",
publisher = "Elsevier Science BV, Amsterdam",
journal = "Colloids and Surfaces B: Biointerfaces",
title = "Properties of diclofenac sodium sorption onto natural zeolite modified with cetylpyridinium chloride",
volume = "83",
number = "1",
pages = "165-172",
doi = "10.1016/j.colsurfb.2010.11.024"
}

Krajišnik, D., Daković, A., Milojević, M., Malenović, A., Kragović, M., Bajuk-Bogdanović, D., Dondur, V.,& Milić, J.. (2011). Properties of diclofenac sodium sorption onto natural zeolite modified with cetylpyridinium chloride. in Colloids and Surfaces B: Biointerfaces
Elsevier Science BV, Amsterdam., 83(1), 165-172.
https://doi.org/10.1016/j.colsurfb.2010.11.024

Krajišnik D, Daković A, Milojević M, Malenović A, Kragović M, Bajuk-Bogdanović D, Dondur V, Milić J. Properties of diclofenac sodium sorption onto natural zeolite modified with cetylpyridinium chloride. in Colloids and Surfaces B: Biointerfaces. 2011;83(1):165-172.
doi:10.1016/j.colsurfb.2010.11.024 .

Krajišnik, Danina, Daković, Aleksandra, Milojević, Maja, Malenović, Anđelija, Kragović, Milan, Bajuk-Bogdanović, Danica, Dondur, Vera, Milić, Jela, "Properties of diclofenac sodium sorption onto natural zeolite modified with cetylpyridinium chloride" in Colloids and Surfaces B: Biointerfaces, 83, no. 1 (2011):165-172,
https://doi.org/10.1016/j.colsurfb.2010.11.024 . .

TY  - JOUR
AU  - Krajišnik, Danina
AU  - Milojević, Maja
AU  - Malenović, Anđelija
AU  - Daković, Aleksandra
AU  - Ibrić, Svetlana
AU  - Savić, Snežana
AU  - Dondur, Vera
AU  - Matijasević, Srdan
AU  - Radulović, Aleksandra
AU  - Daniels, Rolf
AU  - Milić, Jela
PY  - 2010
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/1364
AB  - Context: In this study an investigation of cationic surfactants-modified natural zeolites as drug formulation excipient was performed. Objective: The aim of this work was to carry out a study of the purified natural zeolitic tuff with high amount of clinoptilolite as a potential carrier for molecules of pharmaceutical interest. Materials and methods: Two cationic surfactants (benzalkonium chloride and hexadecyltrimethylammonium bromide) were used for modification of the zeolitic surface in two levels (equal to and twice as external cation-exchange capacity of the zeolitic tuff). Prepared samples were characterized by Fourier transform infrared spectroscopy, thermogravimetric, high-performance liquid chromatography analysis, and powder flow determination. Different surfactant/zeolite composites were used for additional investigation of three model drugs: diclofenac diethylamine, diclofenac sodium, and ibuprofen by means of adsorption isotherm measurements in aqueous solutions. Results: The modified zeolites with two levels of surfactant coverage within the short activation time were prepared. Determination of flow properties showed that modification of zeolitic surface reflected on powder flow characteristics. Investigation of the model drugs adsorption on the obtained composites revealed that a variation between adsorption levels was influenced by the surfactant type and the amount present at the surface of the composites. Discussion and conclusion: In vitro release profiles of the drugs from the zeolite-surfactant-drug composites revealed that sustained drug release could be attained over a period of 8 hours. The presented results for drug uptake by surfactant-zeolite composites and the afterward drug release demonstrated the potential use of investigated modified natural zeolite as excipients for advanced excipients in drug formulations.
PB  - Informa Healthcare, London
T2  - Drug Development and Industrial Pharmacy
T1  - Cationic surfactants-modified natural zeolites: improvement of the excipients functionality
VL  - 36
IS  - 10
SP  - 1215
EP  - 1224
DO  - 10.3109/03639041003695121
ER  - 

@article{
author = "Krajišnik, Danina and Milojević, Maja and Malenović, Anđelija and Daković, Aleksandra and Ibrić, Svetlana and Savić, Snežana and Dondur, Vera and Matijasević, Srdan and Radulović, Aleksandra and Daniels, Rolf and Milić, Jela",
year = "2010",
abstract = "Context: In this study an investigation of cationic surfactants-modified natural zeolites as drug formulation excipient was performed. Objective: The aim of this work was to carry out a study of the purified natural zeolitic tuff with high amount of clinoptilolite as a potential carrier for molecules of pharmaceutical interest. Materials and methods: Two cationic surfactants (benzalkonium chloride and hexadecyltrimethylammonium bromide) were used for modification of the zeolitic surface in two levels (equal to and twice as external cation-exchange capacity of the zeolitic tuff). Prepared samples were characterized by Fourier transform infrared spectroscopy, thermogravimetric, high-performance liquid chromatography analysis, and powder flow determination. Different surfactant/zeolite composites were used for additional investigation of three model drugs: diclofenac diethylamine, diclofenac sodium, and ibuprofen by means of adsorption isotherm measurements in aqueous solutions. Results: The modified zeolites with two levels of surfactant coverage within the short activation time were prepared. Determination of flow properties showed that modification of zeolitic surface reflected on powder flow characteristics. Investigation of the model drugs adsorption on the obtained composites revealed that a variation between adsorption levels was influenced by the surfactant type and the amount present at the surface of the composites. Discussion and conclusion: In vitro release profiles of the drugs from the zeolite-surfactant-drug composites revealed that sustained drug release could be attained over a period of 8 hours. The presented results for drug uptake by surfactant-zeolite composites and the afterward drug release demonstrated the potential use of investigated modified natural zeolite as excipients for advanced excipients in drug formulations.",
publisher = "Informa Healthcare, London",
journal = "Drug Development and Industrial Pharmacy",
title = "Cationic surfactants-modified natural zeolites: improvement of the excipients functionality",
volume = "36",
number = "10",
pages = "1215-1224",
doi = "10.3109/03639041003695121"
}

Krajišnik, D., Milojević, M., Malenović, A., Daković, A., Ibrić, S., Savić, S., Dondur, V., Matijasević, S., Radulović, A., Daniels, R.,& Milić, J.. (2010). Cationic surfactants-modified natural zeolites: improvement of the excipients functionality. in Drug Development and Industrial Pharmacy
Informa Healthcare, London., 36(10), 1215-1224.
https://doi.org/10.3109/03639041003695121

Krajišnik D, Milojević M, Malenović A, Daković A, Ibrić S, Savić S, Dondur V, Matijasević S, Radulović A, Daniels R, Milić J. Cationic surfactants-modified natural zeolites: improvement of the excipients functionality. in Drug Development and Industrial Pharmacy. 2010;36(10):1215-1224.
doi:10.3109/03639041003695121 .

Krajišnik, Danina, Milojević, Maja, Malenović, Anđelija, Daković, Aleksandra, Ibrić, Svetlana, Savić, Snežana, Dondur, Vera, Matijasević, Srdan, Radulović, Aleksandra, Daniels, Rolf, Milić, Jela, "Cationic surfactants-modified natural zeolites: improvement of the excipients functionality" in Drug Development and Industrial Pharmacy, 36, no. 10 (2010):1215-1224,
https://doi.org/10.3109/03639041003695121 . .