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  - Marjanović, Budimir
AU  - Juranić, Ivan O.
AU  - Ćirić-Marjanović, Gordana
AU  - Mojović, M
AU  - Pasti, Igor
AU  - Janošević, Aleksandra
AU  - Trchova, Miroslava
AU  - Holler, P
AU  - Horský, J
PY  - 2012
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/1806
AB  - Novel electroactive paramagnetic ethacridine oligomers were synthesized by the oxidation of ethacridine lactate with ammonium peroxydisulfate in acidic aqueous solution. The oxidative coupling of ethacridine was proved by gel permeation chromatography and MALDI-TOF mass spectrometry demonstrating the presence of oligomeric chains. Theoretical study of the mechanism of oxidation of ethacridine has been based on the semi-empirical quantum chemical computations of heat of formation and ionization energy of ethacridine, protonated ethacridine, generated reactive species and reaction intermediates, taking into account influence of pH and solvation effects. It was revealed that the prevalent ethacridine dimers are N(C6)C5 coupled. The influence of oxidant to monomer mole ratio on the molecular structure and the morphology of ethacridine oligomers has been studied by elemental analysis, FTIR, Raman, EPR and UV-Visible spectroscopies, MALDI-TOF mass spectrometry and scanning electron microscopy. Besides unoxidized monomeric units as prevalent, oligoethacridines contain the iminoquinonoid and newly formed fused phenazine units. The electroactivity of ethacridine oligomers was investigated by cyclic voltammetry.
T2  - Reactive and Functional Polymers
T1  - Chemical oxidative polymerization of ethacridine
VL  - 72
IS  - 1
SP  - 25
EP  - 35
DO  - 10.1016/j.reactfunctpolym.2011.10.002
ER  - 

@article{
author = "Marjanović, Budimir and Juranić, Ivan O. and Ćirić-Marjanović, Gordana and Mojović, M and Pasti, Igor and Janošević, Aleksandra and Trchova, Miroslava and Holler, P and Horský, J",
year = "2012",
abstract = "Novel electroactive paramagnetic ethacridine oligomers were synthesized by the oxidation of ethacridine lactate with ammonium peroxydisulfate in acidic aqueous solution. The oxidative coupling of ethacridine was proved by gel permeation chromatography and MALDI-TOF mass spectrometry demonstrating the presence of oligomeric chains. Theoretical study of the mechanism of oxidation of ethacridine has been based on the semi-empirical quantum chemical computations of heat of formation and ionization energy of ethacridine, protonated ethacridine, generated reactive species and reaction intermediates, taking into account influence of pH and solvation effects. It was revealed that the prevalent ethacridine dimers are N(C6)C5 coupled. The influence of oxidant to monomer mole ratio on the molecular structure and the morphology of ethacridine oligomers has been studied by elemental analysis, FTIR, Raman, EPR and UV-Visible spectroscopies, MALDI-TOF mass spectrometry and scanning electron microscopy. Besides unoxidized monomeric units as prevalent, oligoethacridines contain the iminoquinonoid and newly formed fused phenazine units. The electroactivity of ethacridine oligomers was investigated by cyclic voltammetry.",
journal = "Reactive and Functional Polymers",
title = "Chemical oxidative polymerization of ethacridine",
volume = "72",
number = "1",
pages = "25-35",
doi = "10.1016/j.reactfunctpolym.2011.10.002"
}

Marjanović, B., Juranić, I. O., Ćirić-Marjanović, G., Mojović, M., Pasti, I., Janošević, A., Trchova, M., Holler, P.,& Horský, J.. (2012). Chemical oxidative polymerization of ethacridine. in Reactive and Functional Polymers, 72(1), 25-35.
https://doi.org/10.1016/j.reactfunctpolym.2011.10.002

Marjanović B, Juranić IO, Ćirić-Marjanović G, Mojović M, Pasti I, Janošević A, Trchova M, Holler P, Horský J. Chemical oxidative polymerization of ethacridine. in Reactive and Functional Polymers. 2012;72(1):25-35.
doi:10.1016/j.reactfunctpolym.2011.10.002 .

Marjanović, Budimir, Juranić, Ivan O., Ćirić-Marjanović, Gordana, Mojović, M, Pasti, Igor, Janošević, Aleksandra, Trchova, Miroslava, Holler, P, Horský, J, "Chemical oxidative polymerization of ethacridine" in Reactive and Functional Polymers, 72, no. 1 (2012):25-35,
https://doi.org/10.1016/j.reactfunctpolym.2011.10.002 . .

TY  - JOUR
AU  - Janošević, Aleksandra
AU  - Ćirić-Marjanović, Gordana
AU  - Marjanović, Budimir
AU  - Trchova, Miroslava
AU  - Stejskal, Jaroslav
PY  - 2010
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/1361
AB  - Self-assembled polyaniline nanorods were synthesized by the oxidation of aniline with ammonium peroxydisulfate in an aqueous solution in the presence of 3,5-dinitrosalicylic acid, using the template-free falling-pH method. The effects of the mole ratio of 3,5-dinitrosalicylic acid to aniline, i.e., of starting pH, monomer concentration, and reaction time on the yield of polymerization, molecular-weight distribution, molecular structure, morphology, and conductivity of the prepared polyanilines have been studied by gelpermeation chromatography. elemental analysis, FTIR and Raman spectroscopies, scanning and transmission electron microscopies, and conductivity measurements. The weight-average molecular weights and polydispersity index were in the range 36,400-54,900 and 3.7-7.6, respectively. Synthesized polyaniline nanorods have a diameter of 25-280 nm and a length of 0.2-1.31 mu m, and conductivities in the range (1.2-4.6) x 10(-2) S cm(-1). The formation mechanism of self-assembled polyaniline nanorods has been discussed.
PB  - Elsevier Science BV, Amsterdam
T2  - Materials Letters
T1  - 3,5-Dinitrosalicylic acid-assisted synthesis of self-assembled polyaniline nanorods
VL  - 64
IS  - 21
SP  - 2337
EP  - 2340
DO  - 10.1016/j.matlet.2010.07.041
ER  - 

@article{
author = "Janošević, Aleksandra and Ćirić-Marjanović, Gordana and Marjanović, Budimir and Trchova, Miroslava and Stejskal, Jaroslav",
year = "2010",
abstract = "Self-assembled polyaniline nanorods were synthesized by the oxidation of aniline with ammonium peroxydisulfate in an aqueous solution in the presence of 3,5-dinitrosalicylic acid, using the template-free falling-pH method. The effects of the mole ratio of 3,5-dinitrosalicylic acid to aniline, i.e., of starting pH, monomer concentration, and reaction time on the yield of polymerization, molecular-weight distribution, molecular structure, morphology, and conductivity of the prepared polyanilines have been studied by gelpermeation chromatography. elemental analysis, FTIR and Raman spectroscopies, scanning and transmission electron microscopies, and conductivity measurements. The weight-average molecular weights and polydispersity index were in the range 36,400-54,900 and 3.7-7.6, respectively. Synthesized polyaniline nanorods have a diameter of 25-280 nm and a length of 0.2-1.31 mu m, and conductivities in the range (1.2-4.6) x 10(-2) S cm(-1). The formation mechanism of self-assembled polyaniline nanorods has been discussed.",
publisher = "Elsevier Science BV, Amsterdam",
journal = "Materials Letters",
title = "3,5-Dinitrosalicylic acid-assisted synthesis of self-assembled polyaniline nanorods",
volume = "64",
number = "21",
pages = "2337-2340",
doi = "10.1016/j.matlet.2010.07.041"
}

Janošević, A., Ćirić-Marjanović, G., Marjanović, B., Trchova, M.,& Stejskal, J.. (2010). 3,5-Dinitrosalicylic acid-assisted synthesis of self-assembled polyaniline nanorods. in Materials Letters
Elsevier Science BV, Amsterdam., 64(21), 2337-2340.
https://doi.org/10.1016/j.matlet.2010.07.041

Janošević A, Ćirić-Marjanović G, Marjanović B, Trchova M, Stejskal J. 3,5-Dinitrosalicylic acid-assisted synthesis of self-assembled polyaniline nanorods. in Materials Letters. 2010;64(21):2337-2340.
doi:10.1016/j.matlet.2010.07.041 .

Janošević, Aleksandra, Ćirić-Marjanović, Gordana, Marjanović, Budimir, Trchova, Miroslava, Stejskal, Jaroslav, "3,5-Dinitrosalicylic acid-assisted synthesis of self-assembled polyaniline nanorods" in Materials Letters, 64, no. 21 (2010):2337-2340,
https://doi.org/10.1016/j.matlet.2010.07.041 . .