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  - 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  - Savić, Marjetka
AU  - Janošević-Ležaić, Aleksandra
AU  - Gavrilov, Nemanja
AU  - Pašti, Igor
AU  - Nedić Vasiljević, Bojana
AU  - Krstić, Jugoslav
AU  - Ćirić-Marjanović, Gordana
PY  - 2023
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/4431
AB  - Composites of carbons with metal oxides and metal sulfides have attracted a lot of interest as materials for energy conversion and storage applications. Herein, we report on novel N,O-doped carbon/ZnO/ZnS and N,O-doped carbon/ZnO composites (generally named C-(MOF-5/PANI)), synthesized by the carbonization of metal–organic framework MOF-5/polyaniline (PANI) composites. The produced C-(MOF-5/PANI)s are comprehensively characterized in terms of composition, molecular and crystalline structure, morphology, electrical conductivity, surface area, and electrochemical behavior. The composition and properties of C-(MOF-5/PANI) composites are dictated by the composition of MOF-5/PANI precursors and the form of PANI (conducting emeraldine salt (ES) or nonconducting emeraldine base). The ZnS phase is formed only with the PANI-ES form due to S-containing counter-ions. XRPD revealed that ZnO and ZnS existed as pure wurtzite crystalline phases. PANI and MOF-5 acted synergistically to produce C-(MOF-5/PANI)s with high SBET (up to 609 m2 g−1), electrical conductivity (up to 0.24 S cm−1), and specific capacitance, Cspec, (up to 238.2 F g−1 at 10 mV s−1). Values of Cspec commensurated with N content in C-(MOF-5/PANI) composites (1–10 wt.%) and overcame Cspec of carbonized individual components PANI and MOF-5. By acid etching treatment of C-(MOF-5/PANI), SBET and Cspec increased to 1148 m2 g−1 and 341 F g−1, respectively. The developed composites represent promising electrode materials for supercapacitors.
PB  - MDPI
T2  - Materials
T1  - Carbonization of MOF-5/Polyaniline Composites to N,O-Doped Carbon/ZnO/ZnS and N,O-Doped Carbon/ZnO Composites with High Specific Capacitance, Specific Surface Area and Electrical Conductivity
VL  - 16
IS  - 3
DO  - 10.3390/ma16031018
ER  - 

@article{
author = "Savić, Marjetka and Janošević-Ležaić, Aleksandra and Gavrilov, Nemanja and Pašti, Igor and Nedić Vasiljević, Bojana and Krstić, Jugoslav and Ćirić-Marjanović, Gordana",
year = "2023",
abstract = "Composites of carbons with metal oxides and metal sulfides have attracted a lot of interest as materials for energy conversion and storage applications. Herein, we report on novel N,O-doped carbon/ZnO/ZnS and N,O-doped carbon/ZnO composites (generally named C-(MOF-5/PANI)), synthesized by the carbonization of metal–organic framework MOF-5/polyaniline (PANI) composites. The produced C-(MOF-5/PANI)s are comprehensively characterized in terms of composition, molecular and crystalline structure, morphology, electrical conductivity, surface area, and electrochemical behavior. The composition and properties of C-(MOF-5/PANI) composites are dictated by the composition of MOF-5/PANI precursors and the form of PANI (conducting emeraldine salt (ES) or nonconducting emeraldine base). The ZnS phase is formed only with the PANI-ES form due to S-containing counter-ions. XRPD revealed that ZnO and ZnS existed as pure wurtzite crystalline phases. PANI and MOF-5 acted synergistically to produce C-(MOF-5/PANI)s with high SBET (up to 609 m2 g−1), electrical conductivity (up to 0.24 S cm−1), and specific capacitance, Cspec, (up to 238.2 F g−1 at 10 mV s−1). Values of Cspec commensurated with N content in C-(MOF-5/PANI) composites (1–10 wt.%) and overcame Cspec of carbonized individual components PANI and MOF-5. By acid etching treatment of C-(MOF-5/PANI), SBET and Cspec increased to 1148 m2 g−1 and 341 F g−1, respectively. The developed composites represent promising electrode materials for supercapacitors.",
publisher = "MDPI",
journal = "Materials",
title = "Carbonization of MOF-5/Polyaniline Composites to N,O-Doped Carbon/ZnO/ZnS and N,O-Doped Carbon/ZnO Composites with High Specific Capacitance, Specific Surface Area and Electrical Conductivity",
volume = "16",
number = "3",
doi = "10.3390/ma16031018"
}

Savić, M., Janošević-Ležaić, A., Gavrilov, N., Pašti, I., Nedić Vasiljević, B., Krstić, J.,& Ćirić-Marjanović, G.. (2023). Carbonization of MOF-5/Polyaniline Composites to N,O-Doped Carbon/ZnO/ZnS and N,O-Doped Carbon/ZnO Composites with High Specific Capacitance, Specific Surface Area and Electrical Conductivity. in Materials
MDPI., 16(3).
https://doi.org/10.3390/ma16031018

Savić M, Janošević-Ležaić A, Gavrilov N, Pašti I, Nedić Vasiljević B, Krstić J, Ćirić-Marjanović G. Carbonization of MOF-5/Polyaniline Composites to N,O-Doped Carbon/ZnO/ZnS and N,O-Doped Carbon/ZnO Composites with High Specific Capacitance, Specific Surface Area and Electrical Conductivity. in Materials. 2023;16(3).
doi:10.3390/ma16031018 .

Savić, Marjetka, Janošević-Ležaić, Aleksandra, Gavrilov, Nemanja, Pašti, Igor, Nedić Vasiljević, Bojana, Krstić, Jugoslav, Ćirić-Marjanović, Gordana, "Carbonization of MOF-5/Polyaniline Composites to N,O-Doped Carbon/ZnO/ZnS and N,O-Doped Carbon/ZnO Composites with High Specific Capacitance, Specific Surface Area and Electrical Conductivity" in Materials, 16, no. 3 (2023),
https://doi.org/10.3390/ma16031018 . .

TY  - JOUR
AU  - Janošević-Ležaić, Aleksandra
AU  - Bajuk-Bogdanović, Danica
AU  - Krstić, Jugoslav
AU  - Jovanović, Zoran
AU  - Mravik, Željko
AU  - Kovač, Janez
AU  - Gavrilov, Nemanja
PY  - 2022
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/4070
AB  - Transformation of tannic acid (TA), a cheap, abundant and environmentally friendly (by)product, upon carbonization at various temperatures was examined as it is extensively being used in energy storing devices. In addition of reviling what is happening with TA upon carbonization, a step further has been taken to scrutinize the role of carbonized TA (CTA) playing in energy storage composites. Increasing the carbonization temperature from 500 ◦C to 800 ◦C led to a nine orders of magnitude increase in conductivity, from 9⋅10–9 S cm
PB  - Elsevier Ltd
T2  - Fuel
T1  - What role does carbonized tannic acid play in energy storage composites?
VL  - 312
DO  - 10.1016/j.fuel.2021.122930
ER  - 

@article{
author = "Janošević-Ležaić, Aleksandra and Bajuk-Bogdanović, Danica and Krstić, Jugoslav and Jovanović, Zoran and Mravik, Željko and Kovač, Janez and Gavrilov, Nemanja",
year = "2022",
abstract = "Transformation of tannic acid (TA), a cheap, abundant and environmentally friendly (by)product, upon carbonization at various temperatures was examined as it is extensively being used in energy storing devices. In addition of reviling what is happening with TA upon carbonization, a step further has been taken to scrutinize the role of carbonized TA (CTA) playing in energy storage composites. Increasing the carbonization temperature from 500 ◦C to 800 ◦C led to a nine orders of magnitude increase in conductivity, from 9⋅10–9 S cm",
publisher = "Elsevier Ltd",
journal = "Fuel",
title = "What role does carbonized tannic acid play in energy storage composites?",
volume = "312",
doi = "10.1016/j.fuel.2021.122930"
}

Janošević-Ležaić, A., Bajuk-Bogdanović, D., Krstić, J., Jovanović, Z., Mravik, Ž., Kovač, J.,& Gavrilov, N.. (2022). What role does carbonized tannic acid play in energy storage composites?. in Fuel
Elsevier Ltd., 312.
https://doi.org/10.1016/j.fuel.2021.122930

Janošević-Ležaić A, Bajuk-Bogdanović D, Krstić J, Jovanović Z, Mravik Ž, Kovač J, Gavrilov N. What role does carbonized tannic acid play in energy storage composites?. in Fuel. 2022;312.
doi:10.1016/j.fuel.2021.122930 .

Janošević-Ležaić, Aleksandra, Bajuk-Bogdanović, Danica, Krstić, Jugoslav, Jovanović, Zoran, Mravik, Željko, Kovač, Janez, Gavrilov, Nemanja, "What role does carbonized tannic acid play in energy storage composites?" in Fuel, 312 (2022),
https://doi.org/10.1016/j.fuel.2021.122930 . .

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  - Jauković, Valentina
AU  - Krajišnik, Danina
AU  - Daković, Aleksandra
AU  - Damjanović, Ana
AU  - Krstić, Jugoslav
AU  - Stojanović, Jovica
AU  - Čalija, Bojan
PY  - 2021
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3796
AB  - The functionality of halloysite (Hal) nanotubes as drug carriers can be improved by lumen enlargement and polymer modification. This study investigates the influence of selective acid etching on Hal functionalization with cationic biopolymer chitosan. Hal was subjected to lumen etching under mild conditions, loaded under vacuum with nonsteroidal antiinflammatory drug aceclofenac, and incubated in an acidic solution of chitosan. The functionality of pristine and etched Hal before and upon polymer functionalization was assessed by ζ-potential measurements, structural characterization (FT-IR, DSC and XRPD analysis), cell viability assay, drug loading and drug release studies. Acid etching increased specific surface area, pore volume and pore size of Hal, decreased ζ-potential and facilitated binding of the cationic polymer. XRPD and DSC analysis revealed crystalline structure of etched Hal. Successful chitosan binding and drug entrapment were further confirmed by FT-IR and DSC studies. XRPD showed surface polymer binding. DSC and FT-IR analyses confirmed the presence of the entrapped drug in its crystalline form. Drug loading was increased for ≈81% by selective lumen etching. Slight decrease of drug content occurred during chitosan functionalization due to aceclofenac diffusion in the polymer solution. The drug release was more sustained from etched Hal nanocomposites (up to ≈87% for 12 h) than from pristine Hal (up to ≈97% for 12 h) due to more intensive chitosan binding. High human fibroblast survival rates upon exposure to pristine and etched Hal before and after chitosan functionalization (>90% in the concentration of 1000 μg/mL) confirmed that both lumen etching under mild conditions and polymer functionalization had no significant effect on cytocompatibility. Based on these findings, selective lumen etching in combination with polycation modification appears to be a promising approach for improvement of Hal nanotubes functionality by increasing payload, polymer binding capacity, and sustained release properties with no significant effect on their cytocompatibility.
PB  - Elsevier Ltd
T2  - Materials Science and Engineering C
T1  - Influence of selective acid-etching on functionality of halloysite-chitosan nanocontainers for sustained drug release
VL  - 123
DO  - 10.1016/j.msec.2021.112029
ER  - 

@article{
author = "Jauković, Valentina and Krajišnik, Danina and Daković, Aleksandra and Damjanović, Ana and Krstić, Jugoslav and Stojanović, Jovica and Čalija, Bojan",
year = "2021",
abstract = "The functionality of halloysite (Hal) nanotubes as drug carriers can be improved by lumen enlargement and polymer modification. This study investigates the influence of selective acid etching on Hal functionalization with cationic biopolymer chitosan. Hal was subjected to lumen etching under mild conditions, loaded under vacuum with nonsteroidal antiinflammatory drug aceclofenac, and incubated in an acidic solution of chitosan. The functionality of pristine and etched Hal before and upon polymer functionalization was assessed by ζ-potential measurements, structural characterization (FT-IR, DSC and XRPD analysis), cell viability assay, drug loading and drug release studies. Acid etching increased specific surface area, pore volume and pore size of Hal, decreased ζ-potential and facilitated binding of the cationic polymer. XRPD and DSC analysis revealed crystalline structure of etched Hal. Successful chitosan binding and drug entrapment were further confirmed by FT-IR and DSC studies. XRPD showed surface polymer binding. DSC and FT-IR analyses confirmed the presence of the entrapped drug in its crystalline form. Drug loading was increased for ≈81% by selective lumen etching. Slight decrease of drug content occurred during chitosan functionalization due to aceclofenac diffusion in the polymer solution. The drug release was more sustained from etched Hal nanocomposites (up to ≈87% for 12 h) than from pristine Hal (up to ≈97% for 12 h) due to more intensive chitosan binding. High human fibroblast survival rates upon exposure to pristine and etched Hal before and after chitosan functionalization (>90% in the concentration of 1000 μg/mL) confirmed that both lumen etching under mild conditions and polymer functionalization had no significant effect on cytocompatibility. Based on these findings, selective lumen etching in combination with polycation modification appears to be a promising approach for improvement of Hal nanotubes functionality by increasing payload, polymer binding capacity, and sustained release properties with no significant effect on their cytocompatibility.",
publisher = "Elsevier Ltd",
journal = "Materials Science and Engineering C",
title = "Influence of selective acid-etching on functionality of halloysite-chitosan nanocontainers for sustained drug release",
volume = "123",
doi = "10.1016/j.msec.2021.112029"
}

Jauković, V., Krajišnik, D., Daković, A., Damjanović, A., Krstić, J., Stojanović, J.,& Čalija, B.. (2021). Influence of selective acid-etching on functionality of halloysite-chitosan nanocontainers for sustained drug release. in Materials Science and Engineering C
Elsevier Ltd., 123.
https://doi.org/10.1016/j.msec.2021.112029

Jauković V, Krajišnik D, Daković A, Damjanović A, Krstić J, Stojanović J, Čalija B. Influence of selective acid-etching on functionality of halloysite-chitosan nanocontainers for sustained drug release. in Materials Science and Engineering C. 2021;123.
doi:10.1016/j.msec.2021.112029 .

Jauković, Valentina, Krajišnik, Danina, Daković, Aleksandra, Damjanović, Ana, Krstić, Jugoslav, Stojanović, Jovica, Čalija, Bojan, "Influence of selective acid-etching on functionality of halloysite-chitosan nanocontainers for sustained drug release" in Materials Science and Engineering C, 123 (2021),
https://doi.org/10.1016/j.msec.2021.112029 . .

TY  - JOUR
AU  - Spasojević, Milica
AU  - Daković, Aleksandra
AU  - Rottinghaus, George E.
AU  - Obradović, Milena
AU  - Krajišnik, Danina
AU  - Marković, Marija
AU  - Krstić, Jugoslav
PY  - 2021
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3795
AB  - A natural kaolin from Serbia was modified with different amounts of octadecyldimethylbenzyl ammonium (ODMBA) - (25, 50 and 90% of kaolin cation exchange capacity). Samples were denoted as OKR-25, OKR-50 and OKR-90. Several methods (FTIR spectroscopy, thermal analysis, zeta potential measurements, and N2 physisorption) were used for characterization of the organokaolinites. Adsorption of the common mycotoxins - ochratoxin A (OCHRA) and zearalenone (ZEN) by the organokaolinites was investigated at different levels of solid phase in suspension, different initial mycotoxin concentrations and different pH values. The natural kaolin was not effective in binding OCHRA or ZEN. Adsorption of both mycotoxins by organokaolinites increased with increasing amounts of solid phase as well as with increasing levels of surfactant on the kaolin surface. OCHRA and ZEN adsorption by all organokaolinites followed non-linear adsorption isotherms, at pH 3, 7 and 9. The maximum adsorption capacity for OCHRA adsorption was at pH 3 (4.8 mg/g for OKR-25, 26.7 mg/g for OKR-50 and 39.2 mg/g for OKR-90) that was calculated from the Langmuir model. Much lower OCHRA adsorption capacities were found at pH 7 and 9 (from 0.8 mg/g to 6.9 mg/g at pH 7 and from 1.1 mg/g to 4.6 mg/g at pH 9). The following adsorption capacities for ZEN were obtained from the Langmuir isotherms, at pH 3: 4.5 mg/g for OKR-25, 12.0 mg/g for OKR-50 and 13.5 mg/g for OKR-90. At pH 7, adsorption of ZEN was 5.7 mg/g for OKR-25, 15.3 mg/g for OKR-90 and 14. 4 mg/g for OKR-90. At pH 9, ZEN adsorption capacities were 2.4, 14.1 and 8.1 mg/g for OKR-25, OKR-50 and OKR-90, respectively. Thus, at the lowest amount of ODMBA at the kaolin surface, adsorption of ZEN was similar at pH 3 and 7, while a slightly lower value was obtained for its adsorption at pH 9. With increasing amounts of organic phase at the kaolin surface, the adsorption of ZEN was practically independent of pH. Adsorption of both mycotoxins was dependent on the amount of ODMBA ions at the kaolin surface as well as on their forms in solution.
PB  - Elsevier Ltd
T2  - Applied Clay Science
T1  - Influence of surface coverage of kaolin with surfactant ions on adsorption of ochratoxin A and zearalenone
VL  - 205
DO  - 10.1016/j.clay.2021.106040
ER  - 

@article{
author = "Spasojević, Milica and Daković, Aleksandra and Rottinghaus, George E. and Obradović, Milena and Krajišnik, Danina and Marković, Marija and Krstić, Jugoslav",
year = "2021",
abstract = "A natural kaolin from Serbia was modified with different amounts of octadecyldimethylbenzyl ammonium (ODMBA) - (25, 50 and 90% of kaolin cation exchange capacity). Samples were denoted as OKR-25, OKR-50 and OKR-90. Several methods (FTIR spectroscopy, thermal analysis, zeta potential measurements, and N2 physisorption) were used for characterization of the organokaolinites. Adsorption of the common mycotoxins - ochratoxin A (OCHRA) and zearalenone (ZEN) by the organokaolinites was investigated at different levels of solid phase in suspension, different initial mycotoxin concentrations and different pH values. The natural kaolin was not effective in binding OCHRA or ZEN. Adsorption of both mycotoxins by organokaolinites increased with increasing amounts of solid phase as well as with increasing levels of surfactant on the kaolin surface. OCHRA and ZEN adsorption by all organokaolinites followed non-linear adsorption isotherms, at pH 3, 7 and 9. The maximum adsorption capacity for OCHRA adsorption was at pH 3 (4.8 mg/g for OKR-25, 26.7 mg/g for OKR-50 and 39.2 mg/g for OKR-90) that was calculated from the Langmuir model. Much lower OCHRA adsorption capacities were found at pH 7 and 9 (from 0.8 mg/g to 6.9 mg/g at pH 7 and from 1.1 mg/g to 4.6 mg/g at pH 9). The following adsorption capacities for ZEN were obtained from the Langmuir isotherms, at pH 3: 4.5 mg/g for OKR-25, 12.0 mg/g for OKR-50 and 13.5 mg/g for OKR-90. At pH 7, adsorption of ZEN was 5.7 mg/g for OKR-25, 15.3 mg/g for OKR-90 and 14. 4 mg/g for OKR-90. At pH 9, ZEN adsorption capacities were 2.4, 14.1 and 8.1 mg/g for OKR-25, OKR-50 and OKR-90, respectively. Thus, at the lowest amount of ODMBA at the kaolin surface, adsorption of ZEN was similar at pH 3 and 7, while a slightly lower value was obtained for its adsorption at pH 9. With increasing amounts of organic phase at the kaolin surface, the adsorption of ZEN was practically independent of pH. Adsorption of both mycotoxins was dependent on the amount of ODMBA ions at the kaolin surface as well as on their forms in solution.",
publisher = "Elsevier Ltd",
journal = "Applied Clay Science",
title = "Influence of surface coverage of kaolin with surfactant ions on adsorption of ochratoxin A and zearalenone",
volume = "205",
doi = "10.1016/j.clay.2021.106040"
}

Spasojević, M., Daković, A., Rottinghaus, G. E., Obradović, M., Krajišnik, D., Marković, M.,& Krstić, J.. (2021). Influence of surface coverage of kaolin with surfactant ions on adsorption of ochratoxin A and zearalenone. in Applied Clay Science
Elsevier Ltd., 205.
https://doi.org/10.1016/j.clay.2021.106040

Spasojević M, Daković A, Rottinghaus GE, Obradović M, Krajišnik D, Marković M, Krstić J. Influence of surface coverage of kaolin with surfactant ions on adsorption of ochratoxin A and zearalenone. in Applied Clay Science. 2021;205.
doi:10.1016/j.clay.2021.106040 .

Spasojević, Milica, Daković, Aleksandra, Rottinghaus, George E., Obradović, Milena, Krajišnik, Danina, Marković, Marija, Krstić, Jugoslav, "Influence of surface coverage of kaolin with surfactant ions on adsorption of ochratoxin A and zearalenone" in Applied Clay Science, 205 (2021),
https://doi.org/10.1016/j.clay.2021.106040 . .

TY  - JOUR
AU  - Bajuk-Bogdanovic, Danica
AU  - Holclajtner-Antunović, Ivanka
AU  - Jovanović, Zoran
AU  - Mravik, Željko
AU  - Krstić, Jugoslav
AU  - Uskoković-Marković, Snežana
AU  - Vujkovic, Milica
PY  - 2019
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3455
AB  - The synergistic effects between two Keggin-type heteropoly acids (HPAs) and carbon surface were examined and elucidated. An improved high rate capability (and potential high capacitor electrode for supercapacitors) of the hybrid materials, obtained by anchoring of α-dodecamolybdophosphoric (MoPA), α-dodecatungstophosphoric (WPA), and their mixture to activated carbon (AC), was achieved through the different mechanism of interaction. In order to elaborate this, a detailed analysis of AC-HPA composites has been performed by scanning electron microscopy (SEM), Brunauer–Emmett–Teller (BET) analysis, temperature-programmed desorption (TPD), Fourier-transform infrared spectroscopy (FTIR), micro Raman spectroscopy, and zeta potential measurements. The zeta potential measurements revealed positive charge of carbon surface thus indicating attractive interactions with negatively charged Keggin anion. The surface analysis has shown that WPA spontaneously reduces the carbon surface, while interaction with MoPA leads to its oxidation. As the consequence of the tailoring of the functional groups at carbon surface through HPAs’ action, the distortion of cyclic voltammograms (CVs) decreased in the following order: AC-MoPA, AC-MoPA-WPA, and AC-WPA. A prominent rectangular shape of AC-WPA, even at an extremely high scan rate of 400 mVs−1, was measured, which is rarely demonstrated for carbon-based composites. By applying the theory of electrode potentials, the HPA-AC synergistic effect was explained and discussed in terms of charge storage improvement of HPA-modified carbon.
PB  - Springer
T2  - Journal of Solid State Electrochemistry
T1  - Tailoring the electrochemical charge storage properties of carbonaceous support by redox properties of heteropoly acids: where does the synergy come from?
VL  - 23
IS  - 9
SP  - 2747
EP  - 2758
DO  - 10.1007/s10008-019-04369-4
ER  - 

@article{
author = "Bajuk-Bogdanovic, Danica and Holclajtner-Antunović, Ivanka and Jovanović, Zoran and Mravik, Željko and Krstić, Jugoslav and Uskoković-Marković, Snežana and Vujkovic, Milica",
year = "2019",
abstract = "The synergistic effects between two Keggin-type heteropoly acids (HPAs) and carbon surface were examined and elucidated. An improved high rate capability (and potential high capacitor electrode for supercapacitors) of the hybrid materials, obtained by anchoring of α-dodecamolybdophosphoric (MoPA), α-dodecatungstophosphoric (WPA), and their mixture to activated carbon (AC), was achieved through the different mechanism of interaction. In order to elaborate this, a detailed analysis of AC-HPA composites has been performed by scanning electron microscopy (SEM), Brunauer–Emmett–Teller (BET) analysis, temperature-programmed desorption (TPD), Fourier-transform infrared spectroscopy (FTIR), micro Raman spectroscopy, and zeta potential measurements. The zeta potential measurements revealed positive charge of carbon surface thus indicating attractive interactions with negatively charged Keggin anion. The surface analysis has shown that WPA spontaneously reduces the carbon surface, while interaction with MoPA leads to its oxidation. As the consequence of the tailoring of the functional groups at carbon surface through HPAs’ action, the distortion of cyclic voltammograms (CVs) decreased in the following order: AC-MoPA, AC-MoPA-WPA, and AC-WPA. A prominent rectangular shape of AC-WPA, even at an extremely high scan rate of 400 mVs−1, was measured, which is rarely demonstrated for carbon-based composites. By applying the theory of electrode potentials, the HPA-AC synergistic effect was explained and discussed in terms of charge storage improvement of HPA-modified carbon.",
publisher = "Springer",
journal = "Journal of Solid State Electrochemistry",
title = "Tailoring the electrochemical charge storage properties of carbonaceous support by redox properties of heteropoly acids: where does the synergy come from?",
volume = "23",
number = "9",
pages = "2747-2758",
doi = "10.1007/s10008-019-04369-4"
}

Bajuk-Bogdanovic, D., Holclajtner-Antunović, I., Jovanović, Z., Mravik, Ž., Krstić, J., Uskoković-Marković, S.,& Vujkovic, M.. (2019). Tailoring the electrochemical charge storage properties of carbonaceous support by redox properties of heteropoly acids: where does the synergy come from?. in Journal of Solid State Electrochemistry
Springer., 23(9), 2747-2758.
https://doi.org/10.1007/s10008-019-04369-4

Bajuk-Bogdanovic D, Holclajtner-Antunović I, Jovanović Z, Mravik Ž, Krstić J, Uskoković-Marković S, Vujkovic M. Tailoring the electrochemical charge storage properties of carbonaceous support by redox properties of heteropoly acids: where does the synergy come from?. in Journal of Solid State Electrochemistry. 2019;23(9):2747-2758.
doi:10.1007/s10008-019-04369-4 .

Bajuk-Bogdanovic, Danica, Holclajtner-Antunović, Ivanka, Jovanović, Zoran, Mravik, Željko, Krstić, Jugoslav, Uskoković-Marković, Snežana, Vujkovic, Milica, "Tailoring the electrochemical charge storage properties of carbonaceous support by redox properties of heteropoly acids: where does the synergy come from?" in Journal of Solid State Electrochemistry, 23, no. 9 (2019):2747-2758,
https://doi.org/10.1007/s10008-019-04369-4 . .

TY  - JOUR
AU  - Holclajtner-Antunović, Ivanka
AU  - Bajuk-Bogdanović, Danica
AU  - Popa, Alexandru
AU  - Nedić-Vasiljević, Bojana
AU  - Krstić, Jugoslav
AU  - Mentus, Slavko
AU  - Uskoković-Marković, Snežana
PY  - 2015
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/2470
AB  - The objective of this study is the structural and morphological characterization of the Ag3PW12O40 salts (AgWPA) of 12-tungstophosphoric acid (WPA) obtained under different preparation conditions and testing of their acid catalytic activity in dehydration of ethanol. The structure, morphology and physicochemical characteristics were determined by Fourier transform infrared (FT-IR) and Raman spectroscopy, X-ray diffraction (XRD), nitrogen physisorption at +/- 196 degrees C, scanning electron microscopy (SEM) and differential thermal (DTA) and thermogravimetric analysis (TGA). It is shown that the preparation process has a significant influence on the morphological properties of the obtained materials which may be explained by the supposed mechanism of the formation of nanocrystallite's aggregates with more or less epitaxial connection. Neutral AgWPA obtained by filtration from supernatant forms porous aggregates of a symmetric dodecahedral shape, having average sizes about 2 mu m. This sample shows higher specific area in comparison with the salt obtained by evaporation due to the higher micropore volume, while mesopore volumes are the same for both salts. Thus conversion of ethanol and selectivities of the main products, ethylene and diethyl ether, are almost the same and constant for both prepared salts, while their values are changed over the reaction time for the parent WPA acid.
PB  - Elsevier Science BV, Amsterdam
T2  - Applied Surface Science
T1  - Structural, morphological and catalytic characterization of neutral Ag salt of 12-tungstophosphoric acid: Influence of preparation conditions
VL  - 328
SP  - 466
EP  - 474
DO  - 10.1016/j.apsusc.2014.12.062
ER  - 

@article{
author = "Holclajtner-Antunović, Ivanka and Bajuk-Bogdanović, Danica and Popa, Alexandru and Nedić-Vasiljević, Bojana and Krstić, Jugoslav and Mentus, Slavko and Uskoković-Marković, Snežana",
year = "2015",
abstract = "The objective of this study is the structural and morphological characterization of the Ag3PW12O40 salts (AgWPA) of 12-tungstophosphoric acid (WPA) obtained under different preparation conditions and testing of their acid catalytic activity in dehydration of ethanol. The structure, morphology and physicochemical characteristics were determined by Fourier transform infrared (FT-IR) and Raman spectroscopy, X-ray diffraction (XRD), nitrogen physisorption at +/- 196 degrees C, scanning electron microscopy (SEM) and differential thermal (DTA) and thermogravimetric analysis (TGA). It is shown that the preparation process has a significant influence on the morphological properties of the obtained materials which may be explained by the supposed mechanism of the formation of nanocrystallite's aggregates with more or less epitaxial connection. Neutral AgWPA obtained by filtration from supernatant forms porous aggregates of a symmetric dodecahedral shape, having average sizes about 2 mu m. This sample shows higher specific area in comparison with the salt obtained by evaporation due to the higher micropore volume, while mesopore volumes are the same for both salts. Thus conversion of ethanol and selectivities of the main products, ethylene and diethyl ether, are almost the same and constant for both prepared salts, while their values are changed over the reaction time for the parent WPA acid.",
publisher = "Elsevier Science BV, Amsterdam",
journal = "Applied Surface Science",
title = "Structural, morphological and catalytic characterization of neutral Ag salt of 12-tungstophosphoric acid: Influence of preparation conditions",
volume = "328",
pages = "466-474",
doi = "10.1016/j.apsusc.2014.12.062"
}

Holclajtner-Antunović, I., Bajuk-Bogdanović, D., Popa, A., Nedić-Vasiljević, B., Krstić, J., Mentus, S.,& Uskoković-Marković, S.. (2015). Structural, morphological and catalytic characterization of neutral Ag salt of 12-tungstophosphoric acid: Influence of preparation conditions. in Applied Surface Science
Elsevier Science BV, Amsterdam., 328, 466-474.
https://doi.org/10.1016/j.apsusc.2014.12.062

Holclajtner-Antunović I, Bajuk-Bogdanović D, Popa A, Nedić-Vasiljević B, Krstić J, Mentus S, Uskoković-Marković S. Structural, morphological and catalytic characterization of neutral Ag salt of 12-tungstophosphoric acid: Influence of preparation conditions. in Applied Surface Science. 2015;328:466-474.
doi:10.1016/j.apsusc.2014.12.062 .

Holclajtner-Antunović, Ivanka, Bajuk-Bogdanović, Danica, Popa, Alexandru, Nedić-Vasiljević, Bojana, Krstić, Jugoslav, Mentus, Slavko, Uskoković-Marković, Snežana, "Structural, morphological and catalytic characterization of neutral Ag salt of 12-tungstophosphoric acid: Influence of preparation conditions" in Applied Surface Science, 328 (2015):466-474,
https://doi.org/10.1016/j.apsusc.2014.12.062 . .

TY  - JOUR
AU  - Janićijević, Jelena
AU  - Krajišnik, Danina
AU  - Čalija, Bojan
AU  - Dobričić, Vladimir
AU  - Daković, Aleksandra
AU  - Krstić, Jugoslav
AU  - Marković, Marija
AU  - Milić, Jela
PY  - 2014
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/2101
AB  - Inorganic modification of diatomite was performed with the precipitation product of partially neutralized aluminum sulfate solution at three different mass ratios. The starting and the modified diatomites were characterized by SEM-EDS, FTIR, thermal analysis and zeta potential measurements and evaluated for drug loading capacity in adsorption batch experiments using diclofenac sodium (DS) as a model drug. In vitro drug release studies were performed in phosphate buffer pH 6.8 from comprimates containing: the drug adsorbed onto the selected modified diatomite sample (DAMD), physical mixture of the drug with the selected modified diatomite sample (PMDMD) and physical mixture of the drug with the starting diatomite (PMDD). In vivo acute toxicity testing of the modified diatomite samples was performed on mice. High adsorbent loading of the selected modified diatomite sample (similar to 250 mg/g in 2 h) enabled the preparation of comprimates containing adsorbed DS in the amount near to its therapeutic dose. Drug release studies demonstrated prolonged release of DS over a period of 8 h from both DAMD comprimates (18% after 8 h) and PMDMD comprimates (45% after 8 h). The release kinetics for DAMD and PMDMD comprimates fitted well with Korsmeyer-Peppas and Bhaskar models, indicating that the release mechanism was a combination of non-Fickian diffusion and ion exchange process.
PB  - Elsevier Science BV, Amsterdam
T2  - Materials Science & Engineering C: Materials for Biological Applications
T1  - Inorganically modified diatomite as a potential prolonged-release drug carrier
VL  - 42
SP  - 412
EP  - 420
DO  - 10.1016/j.msec.2014.05.052
ER  - 

@article{
author = "Janićijević, Jelena and Krajišnik, Danina and Čalija, Bojan and Dobričić, Vladimir and Daković, Aleksandra and Krstić, Jugoslav and Marković, Marija and Milić, Jela",
year = "2014",
abstract = "Inorganic modification of diatomite was performed with the precipitation product of partially neutralized aluminum sulfate solution at three different mass ratios. The starting and the modified diatomites were characterized by SEM-EDS, FTIR, thermal analysis and zeta potential measurements and evaluated for drug loading capacity in adsorption batch experiments using diclofenac sodium (DS) as a model drug. In vitro drug release studies were performed in phosphate buffer pH 6.8 from comprimates containing: the drug adsorbed onto the selected modified diatomite sample (DAMD), physical mixture of the drug with the selected modified diatomite sample (PMDMD) and physical mixture of the drug with the starting diatomite (PMDD). In vivo acute toxicity testing of the modified diatomite samples was performed on mice. High adsorbent loading of the selected modified diatomite sample (similar to 250 mg/g in 2 h) enabled the preparation of comprimates containing adsorbed DS in the amount near to its therapeutic dose. Drug release studies demonstrated prolonged release of DS over a period of 8 h from both DAMD comprimates (18% after 8 h) and PMDMD comprimates (45% after 8 h). The release kinetics for DAMD and PMDMD comprimates fitted well with Korsmeyer-Peppas and Bhaskar models, indicating that the release mechanism was a combination of non-Fickian diffusion and ion exchange process.",
publisher = "Elsevier Science BV, Amsterdam",
journal = "Materials Science & Engineering C: Materials for Biological Applications",
title = "Inorganically modified diatomite as a potential prolonged-release drug carrier",
volume = "42",
pages = "412-420",
doi = "10.1016/j.msec.2014.05.052"
}

Janićijević, J., Krajišnik, D., Čalija, B., Dobričić, V., Daković, A., Krstić, J., Marković, M.,& Milić, J.. (2014). Inorganically modified diatomite as a potential prolonged-release drug carrier. in Materials Science & Engineering C: Materials for Biological Applications
Elsevier Science BV, Amsterdam., 42, 412-420.
https://doi.org/10.1016/j.msec.2014.05.052

Janićijević J, Krajišnik D, Čalija B, Dobričić V, Daković A, Krstić J, Marković M, Milić J. Inorganically modified diatomite as a potential prolonged-release drug carrier. in Materials Science & Engineering C: Materials for Biological Applications. 2014;42:412-420.
doi:10.1016/j.msec.2014.05.052 .

Janićijević, Jelena, Krajišnik, Danina, Čalija, Bojan, Dobričić, Vladimir, Daković, Aleksandra, Krstić, Jugoslav, Marković, Marija, Milić, Jela, "Inorganically modified diatomite as a potential prolonged-release drug carrier" in Materials Science & Engineering C: Materials for Biological Applications, 42 (2014):412-420,
https://doi.org/10.1016/j.msec.2014.05.052 . .

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  - Janošević, Aleksandra
AU  - Pasti, Igor
AU  - Gavrilov, Nemanja
AU  - Mentus, Slavko
AU  - Krstić, Jugoslav
AU  - Mitrić, Miodrag
AU  - Travas-Sejdić, Jadranka
AU  - Ćirić-Marjanović, Gordana
PY  - 2012
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/1726
AB  - Microporous conducting nitrogen-containing nanostructured carbon with excellent catalytic activity for the electrochemical synthesis of hydrogen peroxide was synthesized by the carbonization of self-assembled polyaniline 3,5-dinitrosalicylate nanorods. Carbonization was carried out by means of gradual heating in a nitrogen atmosphere up to 800 degrees C. Carbonized polyaniline nanorods containing 9.8 wt.% of nitrogen had a conductivity of 0.35 S cm(-1). The electrical characteristics, morphology, textural parameters, elemental composition, molecular structure and crystallinity of novel carbonized nanostructured polyaniline were investigated by conductivity measurements, scanning and transmission electron microscopies, nitrogen adsorption-desorption measurements, elemental microanalysis, XPS, FTIR and Raman spectroscopies, and XRD, respectively. The electrocatalytic activity of carbonized polyaniline nanorods towards oxygen reduction in alkaline conditions has been studied by the voltammetry with the rotating disk electrode.
PB  - Elsevier Science BV, Amsterdam
T2  - Microporous and Mesoporous Materials
T1  - Microporous conducting carbonized polyaniline nanorods: Synthesis, characterization and electrocatalytic properties
VL  - 152
SP  - 50
EP  - 57
DO  - 10.1016/j.micromeso.2011.12.002
ER  - 

@article{
author = "Janošević, Aleksandra and Pasti, Igor and Gavrilov, Nemanja and Mentus, Slavko and Krstić, Jugoslav and Mitrić, Miodrag and Travas-Sejdić, Jadranka and Ćirić-Marjanović, Gordana",
year = "2012",
abstract = "Microporous conducting nitrogen-containing nanostructured carbon with excellent catalytic activity for the electrochemical synthesis of hydrogen peroxide was synthesized by the carbonization of self-assembled polyaniline 3,5-dinitrosalicylate nanorods. Carbonization was carried out by means of gradual heating in a nitrogen atmosphere up to 800 degrees C. Carbonized polyaniline nanorods containing 9.8 wt.% of nitrogen had a conductivity of 0.35 S cm(-1). The electrical characteristics, morphology, textural parameters, elemental composition, molecular structure and crystallinity of novel carbonized nanostructured polyaniline were investigated by conductivity measurements, scanning and transmission electron microscopies, nitrogen adsorption-desorption measurements, elemental microanalysis, XPS, FTIR and Raman spectroscopies, and XRD, respectively. The electrocatalytic activity of carbonized polyaniline nanorods towards oxygen reduction in alkaline conditions has been studied by the voltammetry with the rotating disk electrode.",
publisher = "Elsevier Science BV, Amsterdam",
journal = "Microporous and Mesoporous Materials",
title = "Microporous conducting carbonized polyaniline nanorods: Synthesis, characterization and electrocatalytic properties",
volume = "152",
pages = "50-57",
doi = "10.1016/j.micromeso.2011.12.002"
}

Janošević, A., Pasti, I., Gavrilov, N., Mentus, S., Krstić, J., Mitrić, M., Travas-Sejdić, J.,& Ćirić-Marjanović, G.. (2012). Microporous conducting carbonized polyaniline nanorods: Synthesis, characterization and electrocatalytic properties. in Microporous and Mesoporous Materials
Elsevier Science BV, Amsterdam., 152, 50-57.
https://doi.org/10.1016/j.micromeso.2011.12.002

Janošević A, Pasti I, Gavrilov N, Mentus S, Krstić J, Mitrić M, Travas-Sejdić J, Ćirić-Marjanović G. Microporous conducting carbonized polyaniline nanorods: Synthesis, characterization and electrocatalytic properties. in Microporous and Mesoporous Materials. 2012;152:50-57.
doi:10.1016/j.micromeso.2011.12.002 .

Janošević, Aleksandra, Pasti, Igor, Gavrilov, Nemanja, Mentus, Slavko, Krstić, Jugoslav, Mitrić, Miodrag, Travas-Sejdić, Jadranka, Ćirić-Marjanović, Gordana, "Microporous conducting carbonized polyaniline nanorods: Synthesis, characterization and electrocatalytic properties" in Microporous and Mesoporous Materials, 152 (2012):50-57,
https://doi.org/10.1016/j.micromeso.2011.12.002 . .

TY  - JOUR
AU  - Janošević, Aleksandra
AU  - Pasti, Igor
AU  - Gavrilov, Nemanja
AU  - Mentus, Slavko
AU  - Ćirić-Marjanović, Gordana
AU  - Krstić, Jugoslav
AU  - Stejskal, Jaroslav
PY  - 2011
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/1594
AB  - Micro/mesoporous conducting nitrogen-containing carbon nanorods/nanotubes with high surface area, and excellent electrocatalytic activity for the oxygen reduction reaction, were synthesized by the carbonization of self-assembled polyaniline (PANI) 5-sulfosalicylate nanorods/nanotubes. Carbonization was carried out by means of gradual heating in a nitrogen atmosphere up to 800 °C. The morphology of the PANI 5-sulfosalicylate was preserved after carbonization. Carbonized PANI nanostructures containing ∼10 wt% of nitrogen had a conductivity of 0.8 S cm-1. The influence of the carbonization on the porosity and specific surface area of the nanostructured PANI has been analyzed. The morphology, elemental composition, molecular structure, surface area, and electrical characteristics of novel carbonized nanostructured PANI were investigated by scanning and transmission electron microscopies, elemental microanalysis, FTIR and Raman spectroscopies, nitrogen adsorption-desorption and conductivity measurements, respectively. The electrocatalytic activity of carbonized PANI 5-sulfosalicylate nanorods/nanotubes material towards oxygen reduction reaction in alkaline conditions has been studied by the voltammetry with the rotating disc electrode.
T2  - Synthetic Metals
T1  - Micro/mesoporous conducting carbonized polyaniline 5-sulfosalicylate nanorods/nanotubes: Synthesis, characterization and electrocatalysis
VL  - 161
IS  - 19-20
SP  - 2179
EP  - 2184
DO  - 10.1016/j.synthmet.2011.08.028
ER  - 

@article{
author = "Janošević, Aleksandra and Pasti, Igor and Gavrilov, Nemanja and Mentus, Slavko and Ćirić-Marjanović, Gordana and Krstić, Jugoslav and Stejskal, Jaroslav",
year = "2011",
abstract = "Micro/mesoporous conducting nitrogen-containing carbon nanorods/nanotubes with high surface area, and excellent electrocatalytic activity for the oxygen reduction reaction, were synthesized by the carbonization of self-assembled polyaniline (PANI) 5-sulfosalicylate nanorods/nanotubes. Carbonization was carried out by means of gradual heating in a nitrogen atmosphere up to 800 °C. The morphology of the PANI 5-sulfosalicylate was preserved after carbonization. Carbonized PANI nanostructures containing ∼10 wt% of nitrogen had a conductivity of 0.8 S cm-1. The influence of the carbonization on the porosity and specific surface area of the nanostructured PANI has been analyzed. The morphology, elemental composition, molecular structure, surface area, and electrical characteristics of novel carbonized nanostructured PANI were investigated by scanning and transmission electron microscopies, elemental microanalysis, FTIR and Raman spectroscopies, nitrogen adsorption-desorption and conductivity measurements, respectively. The electrocatalytic activity of carbonized PANI 5-sulfosalicylate nanorods/nanotubes material towards oxygen reduction reaction in alkaline conditions has been studied by the voltammetry with the rotating disc electrode.",
journal = "Synthetic Metals",
title = "Micro/mesoporous conducting carbonized polyaniline 5-sulfosalicylate nanorods/nanotubes: Synthesis, characterization and electrocatalysis",
volume = "161",
number = "19-20",
pages = "2179-2184",
doi = "10.1016/j.synthmet.2011.08.028"
}

Janošević, A., Pasti, I., Gavrilov, N., Mentus, S., Ćirić-Marjanović, G., Krstić, J.,& Stejskal, J.. (2011). Micro/mesoporous conducting carbonized polyaniline 5-sulfosalicylate nanorods/nanotubes: Synthesis, characterization and electrocatalysis. in Synthetic Metals, 161(19-20), 2179-2184.
https://doi.org/10.1016/j.synthmet.2011.08.028

Janošević A, Pasti I, Gavrilov N, Mentus S, Ćirić-Marjanović G, Krstić J, Stejskal J. Micro/mesoporous conducting carbonized polyaniline 5-sulfosalicylate nanorods/nanotubes: Synthesis, characterization and electrocatalysis. in Synthetic Metals. 2011;161(19-20):2179-2184.
doi:10.1016/j.synthmet.2011.08.028 .

Janošević, Aleksandra, Pasti, Igor, Gavrilov, Nemanja, Mentus, Slavko, Ćirić-Marjanović, Gordana, Krstić, Jugoslav, Stejskal, Jaroslav, "Micro/mesoporous conducting carbonized polyaniline 5-sulfosalicylate nanorods/nanotubes: Synthesis, characterization and electrocatalysis" in Synthetic Metals, 161, no. 19-20 (2011):2179-2184,
https://doi.org/10.1016/j.synthmet.2011.08.028 . .