TY  - JOUR
AU  - Matović, Luka
AU  - Tasić, Nikola
AU  - Trišović, Nemanja
AU  - Lađarević, Jelena
AU  - Vitnik, Vesna
AU  - Vitnik, Željko
AU  - Grgur, Branimir N.
AU  - Mijin, Dušan
PY  - 2019
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/3242
PB  - The Scientific and Technological Research Council of Turkey  (TÜBİTAK)
T2  - Turkish Journal of Chemistry
T1  - On the azo dyes derived from benzoic and cinnamic acids used as photosensitizersin dye-sensitized solar cells
VL  - 43
IS  - 4
SP  - 1183
EP  - 1203
DO  - 10.3906/kim-1903-76
ER  - 

@article{
author = "Matović, Luka and Tasić, Nikola and Trišović, Nemanja and Lađarević, Jelena and Vitnik, Vesna and Vitnik, Željko and Grgur, Branimir N. and Mijin, Dušan",
year = "2019",
publisher = "The Scientific and Technological Research Council of Turkey  (TÜBİTAK)",
journal = "Turkish Journal of Chemistry",
title = "On the azo dyes derived from benzoic and cinnamic acids used as photosensitizersin dye-sensitized solar cells",
volume = "43",
number = "4",
pages = "1183-1203",
doi = "10.3906/kim-1903-76"
}

Matović, L., Tasić, N., Trišović, N., Lađarević, J., Vitnik, V., Vitnik, Ž., Grgur, B. N.,& Mijin, D.. (2019). On the azo dyes derived from benzoic and cinnamic acids used as photosensitizersin dye-sensitized solar cells. in Turkish Journal of Chemistry
The Scientific and Technological Research Council of Turkey  (TÜBİTAK)., 43(4), 1183-1203.
https://doi.org/10.3906/kim-1903-76

Matović L, Tasić N, Trišović N, Lađarević J, Vitnik V, Vitnik Ž, Grgur BN, Mijin D. On the azo dyes derived from benzoic and cinnamic acids used as photosensitizersin dye-sensitized solar cells. in Turkish Journal of Chemistry. 2019;43(4):1183-1203.
doi:10.3906/kim-1903-76 .

Matović, Luka, Tasić, Nikola, Trišović, Nemanja, Lađarević, Jelena, Vitnik, Vesna, Vitnik, Željko, Grgur, Branimir N., Mijin, Dušan, "On the azo dyes derived from benzoic and cinnamic acids used as photosensitizersin dye-sensitized solar cells" in Turkish Journal of Chemistry, 43, no. 4 (2019):1183-1203,
https://doi.org/10.3906/kim-1903-76 . .

TY  - JOUR
AU  - Jokić, Bojan
AU  - Džunuzović, Enis S.
AU  - Grgur, Branimir N.
AU  - Jugović, Branimir
AU  - Trišović, Tomislav
AU  - Stevanović, Jasmina
AU  - Gvozdenović, Milica M.
PY  - 2017
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2173
AB  - Poly(aniline-co-(m-aminobenzoic acid)) was synthesized electrochemically at graphite electrode under galvanostatic conditions. Aqueous electrolyte for synthesis was consisted of HCl and different amount of aniline and m-aminobenzoic acid. The presence of the meta positioned carboxylic group in m-aminobenzoic acid influenced higher co-polymerization potential, different morphology and electrochemical behavior of copolymers compared to polyaniline. Electrochemical activity is achieved by proton exchange in neutral environment that can result in a faster charge/discharge process, which is in the case of PANI limited by slow anion exchange, making this material promising for consideration in super-capacitors and in biological system.
PB  - Springer, Dordrecht
T2  - Journal of Polymer Research
T1  - The influence of m-aminobenzoic acid on electrochemical synthesis and behavior of poly(aniline-co-(m-aminobenzoic acid)
VL  - 24
IS  - 9
DO  - 10.1007/s10965-017-1313-5
ER  - 

@article{
author = "Jokić, Bojan and Džunuzović, Enis S. and Grgur, Branimir N. and Jugović, Branimir and Trišović, Tomislav and Stevanović, Jasmina and Gvozdenović, Milica M.",
year = "2017",
abstract = "Poly(aniline-co-(m-aminobenzoic acid)) was synthesized electrochemically at graphite electrode under galvanostatic conditions. Aqueous electrolyte for synthesis was consisted of HCl and different amount of aniline and m-aminobenzoic acid. The presence of the meta positioned carboxylic group in m-aminobenzoic acid influenced higher co-polymerization potential, different morphology and electrochemical behavior of copolymers compared to polyaniline. Electrochemical activity is achieved by proton exchange in neutral environment that can result in a faster charge/discharge process, which is in the case of PANI limited by slow anion exchange, making this material promising for consideration in super-capacitors and in biological system.",
publisher = "Springer, Dordrecht",
journal = "Journal of Polymer Research",
title = "The influence of m-aminobenzoic acid on electrochemical synthesis and behavior of poly(aniline-co-(m-aminobenzoic acid)",
volume = "24",
number = "9",
doi = "10.1007/s10965-017-1313-5"
}

Jokić, B., Džunuzović, E. S., Grgur, B. N., Jugović, B., Trišović, T., Stevanović, J.,& Gvozdenović, M. M.. (2017). The influence of m-aminobenzoic acid on electrochemical synthesis and behavior of poly(aniline-co-(m-aminobenzoic acid). in Journal of Polymer Research
Springer, Dordrecht., 24(9).
https://doi.org/10.1007/s10965-017-1313-5

Jokić B, Džunuzović ES, Grgur BN, Jugović B, Trišović T, Stevanović J, Gvozdenović MM. The influence of m-aminobenzoic acid on electrochemical synthesis and behavior of poly(aniline-co-(m-aminobenzoic acid). in Journal of Polymer Research. 2017;24(9).
doi:10.1007/s10965-017-1313-5 .

Jokić, Bojan, Džunuzović, Enis S., Grgur, Branimir N., Jugović, Branimir, Trišović, Tomislav, Stevanović, Jasmina, Gvozdenović, Milica M., "The influence of m-aminobenzoic acid on electrochemical synthesis and behavior of poly(aniline-co-(m-aminobenzoic acid)" in Journal of Polymer Research, 24, no. 9 (2017),
https://doi.org/10.1007/s10965-017-1313-5 . .

TY  - JOUR
AU  - Tomković, Tanja
AU  - Radovanović, Filip
AU  - Grgur, Branimir N.
AU  - Nastasović, Aleksandra
AU  - Vasiljević-Radović, Dana
AU  - Onjia, Antonije E.
PY  - 2016
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2018
AB  - A novel method combining a traditional immersion precipitation process for making membranes with photopolymerization and crosslinking of functional monomers included in the casting solution was used to prepare asymmetric polyethersulfone membranes with submicron particles incorporating glycidyl methacrylate copolymer. In order to introduce sulfonic groups, the epoxide rings of glycidyl methacrylate were opened using two methods. The first method was functionalization with sodium sulfite, and the second was functionalization with sulfuric acid and then grafting with 2-acrylamido-2-methylpropanesulfonic acid. The obtained membranes were characterized using infrared spectroscopy, conductometric titration and water permeability measurements. Scanning electron microscopy and atomic force microscopy were used to investigate the surface morphology and topology of the membranes. Dynamic adsorption of rhodamine B as a model dye was used to demonstrate the suitability of these novel membranes for membrane adsorption since the adsorption capacity for dye cations was much better for the membranes functionalized with sodium sulfite and the membranes grafted with 2-acrylamido-2-methylpropanesulfonic acid compared to the non-functionalized membranes.
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Novel negatively charged membrane adsorbers made using a combination of photopolymerization and immersion precipitation
VL  - 81
IS  - 4
SP  - 419
EP  - 431
DO  - 10.2298/JSC150805083T
ER  - 

@article{
author = "Tomković, Tanja and Radovanović, Filip and Grgur, Branimir N. and Nastasović, Aleksandra and Vasiljević-Radović, Dana and Onjia, Antonije E.",
year = "2016",
abstract = "A novel method combining a traditional immersion precipitation process for making membranes with photopolymerization and crosslinking of functional monomers included in the casting solution was used to prepare asymmetric polyethersulfone membranes with submicron particles incorporating glycidyl methacrylate copolymer. In order to introduce sulfonic groups, the epoxide rings of glycidyl methacrylate were opened using two methods. The first method was functionalization with sodium sulfite, and the second was functionalization with sulfuric acid and then grafting with 2-acrylamido-2-methylpropanesulfonic acid. The obtained membranes were characterized using infrared spectroscopy, conductometric titration and water permeability measurements. Scanning electron microscopy and atomic force microscopy were used to investigate the surface morphology and topology of the membranes. Dynamic adsorption of rhodamine B as a model dye was used to demonstrate the suitability of these novel membranes for membrane adsorption since the adsorption capacity for dye cations was much better for the membranes functionalized with sodium sulfite and the membranes grafted with 2-acrylamido-2-methylpropanesulfonic acid compared to the non-functionalized membranes.",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Novel negatively charged membrane adsorbers made using a combination of photopolymerization and immersion precipitation",
volume = "81",
number = "4",
pages = "419-431",
doi = "10.2298/JSC150805083T"
}

Tomković, T., Radovanović, F., Grgur, B. N., Nastasović, A., Vasiljević-Radović, D.,& Onjia, A. E.. (2016). Novel negatively charged membrane adsorbers made using a combination of photopolymerization and immersion precipitation. in Journal of the Serbian Chemical Society
Serbian Chemical Society., 81(4), 419-431.
https://doi.org/10.2298/JSC150805083T

Tomković T, Radovanović F, Grgur BN, Nastasović A, Vasiljević-Radović D, Onjia AE. Novel negatively charged membrane adsorbers made using a combination of photopolymerization and immersion precipitation. in Journal of the Serbian Chemical Society. 2016;81(4):419-431.
doi:10.2298/JSC150805083T .

Tomković, Tanja, Radovanović, Filip, Grgur, Branimir N., Nastasović, Aleksandra, Vasiljević-Radović, Dana, Onjia, Antonije E., "Novel negatively charged membrane adsorbers made using a combination of photopolymerization and immersion precipitation" in Journal of the Serbian Chemical Society, 81, no. 4 (2016):419-431,
https://doi.org/10.2298/JSC150805083T . .

TY  - JOUR
AU  - Radoman, Tijana S
AU  - Džunuzović, Jasna
AU  - Grgur, Branimir N.
AU  - Gvozdenović, Milica M.
AU  - Jugović, Branimir
AU  - Milicevic, Dejan S
AU  - Džunuzović, Enis S.
PY  - 2016
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1915
AB  - Novel TiO2-PANI core-shell nanocomposite, prepared by in situ oxidative polymerization of aniline in the presence of TiO2 nanoparticles surface modified with vitamin B6, was used to reinforce epoxy resin. The size of prepared TiO2 nanoparticles and TiO2-PANI nanocomposite were determined by a transmission electron microscopy (TEM). The surface modification of TiO2 nanoparticles was confirmed by FTIR and UV-vis spectroscopy, while the morphology of PANI and TiO2-PANI nanocomposite was investigated by scanning electron microscopy (SEM). The influence of TiO2-PANI nanocomposite on glass transition temperature, dielectric and dynamic mechanical properties, thermooxidative stability, mechanical and anticorrosion properties of epoxy based nanocomposites was investigated and compared to the properties of epoxy/PANI nanocomposites. It has been observed that the glass transition temperature of epoxy resin increases after introduction of PANI and TiO2-PANI nanocomposite, as well as with increasing their content. Prepared nanocomposites exhibited higher value of dielectric constant than pure epoxy resin. Epoxy based coating containing TiO2-PANI nanocomposite showed lower dielectric loss, higher hardness and better anticorrosion properties than pure epoxy resin and epoxy/PANI nanocomposite.
PB  - Elsevier Science Sa, Lausanne
T2  - Progress in Organic Coatings
T1  - Improvement of the epoxy coating properties by incorporation of polyaniline surface treated TiO2 nanoparticles previously modified with vitamin B6
VL  - 99
SP  - 346
EP  - 355
DO  - 10.1016/j.porgcoat.2016.06.014
ER  - 

@article{
author = "Radoman, Tijana S and Džunuzović, Jasna and Grgur, Branimir N. and Gvozdenović, Milica M. and Jugović, Branimir and Milicevic, Dejan S and Džunuzović, Enis S.",
year = "2016",
abstract = "Novel TiO2-PANI core-shell nanocomposite, prepared by in situ oxidative polymerization of aniline in the presence of TiO2 nanoparticles surface modified with vitamin B6, was used to reinforce epoxy resin. The size of prepared TiO2 nanoparticles and TiO2-PANI nanocomposite were determined by a transmission electron microscopy (TEM). The surface modification of TiO2 nanoparticles was confirmed by FTIR and UV-vis spectroscopy, while the morphology of PANI and TiO2-PANI nanocomposite was investigated by scanning electron microscopy (SEM). The influence of TiO2-PANI nanocomposite on glass transition temperature, dielectric and dynamic mechanical properties, thermooxidative stability, mechanical and anticorrosion properties of epoxy based nanocomposites was investigated and compared to the properties of epoxy/PANI nanocomposites. It has been observed that the glass transition temperature of epoxy resin increases after introduction of PANI and TiO2-PANI nanocomposite, as well as with increasing their content. Prepared nanocomposites exhibited higher value of dielectric constant than pure epoxy resin. Epoxy based coating containing TiO2-PANI nanocomposite showed lower dielectric loss, higher hardness and better anticorrosion properties than pure epoxy resin and epoxy/PANI nanocomposite.",
publisher = "Elsevier Science Sa, Lausanne",
journal = "Progress in Organic Coatings",
title = "Improvement of the epoxy coating properties by incorporation of polyaniline surface treated TiO2 nanoparticles previously modified with vitamin B6",
volume = "99",
pages = "346-355",
doi = "10.1016/j.porgcoat.2016.06.014"
}

Radoman, T. S., Džunuzović, J., Grgur, B. N., Gvozdenović, M. M., Jugović, B., Milicevic, D. S.,& Džunuzović, E. S.. (2016). Improvement of the epoxy coating properties by incorporation of polyaniline surface treated TiO2 nanoparticles previously modified with vitamin B6. in Progress in Organic Coatings
Elsevier Science Sa, Lausanne., 99, 346-355.
https://doi.org/10.1016/j.porgcoat.2016.06.014

Radoman TS, Džunuzović J, Grgur BN, Gvozdenović MM, Jugović B, Milicevic DS, Džunuzović ES. Improvement of the epoxy coating properties by incorporation of polyaniline surface treated TiO2 nanoparticles previously modified with vitamin B6. in Progress in Organic Coatings. 2016;99:346-355.
doi:10.1016/j.porgcoat.2016.06.014 .

Radoman, Tijana S, Džunuzović, Jasna, Grgur, Branimir N., Gvozdenović, Milica M., Jugović, Branimir, Milicevic, Dejan S, Džunuzović, Enis S., "Improvement of the epoxy coating properties by incorporation of polyaniline surface treated TiO2 nanoparticles previously modified with vitamin B6" in Progress in Organic Coatings, 99 (2016):346-355,
https://doi.org/10.1016/j.porgcoat.2016.06.014 . .

TY  - JOUR
AU  - Jugović, Branimir
AU  - Grgur, Branimir N.
AU  - Antov, Mirjana
AU  - Knežević-Jugović, Zorica
AU  - Stevanović, Jasmina
AU  - Gvozdenović, Milica M.
PY  - 2016
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1962
AB  - Polypyrrole enzyme electrode was formed by immobilization of glucose oxidase via glutaraldehyde into electrochemically synthesized polypyrrole on glassy carbon electrode. Electrochemical synthesis was performed in 0.5 mol dm(-3) HCl and 0.2 mol dm(-3) pyrrole at constant current density of 2 mA cm(-2). Chronopotentiometric curves of polypyrrole enzyme electrode were recorded at current density of 42 nA cm(-2) for different glucose concentrations. The determined value of the apparent Michaelis-Menten constant was 0.045 mmol dm(-3) which is significantly lower than that of free enzyme indicating enhanced enzyme efficiency when it is immobilized into electroconducting polymer matrix.
PB  - Esg, Belgrade
T2  - International Journal of Electrochemical Science
T1  - Polypyrrole-based Enzyme Electrode with Immobilized Glucose Oxidase for Electrochemical Determination of Glucose
VL  - 11
IS  - 2
SP  - 1152
EP  - 1161
UR  - https://hdl.handle.net/21.15107/rcub_dais_15979
ER  - 

@article{
author = "Jugović, Branimir and Grgur, Branimir N. and Antov, Mirjana and Knežević-Jugović, Zorica and Stevanović, Jasmina and Gvozdenović, Milica M.",
year = "2016",
abstract = "Polypyrrole enzyme electrode was formed by immobilization of glucose oxidase via glutaraldehyde into electrochemically synthesized polypyrrole on glassy carbon electrode. Electrochemical synthesis was performed in 0.5 mol dm(-3) HCl and 0.2 mol dm(-3) pyrrole at constant current density of 2 mA cm(-2). Chronopotentiometric curves of polypyrrole enzyme electrode were recorded at current density of 42 nA cm(-2) for different glucose concentrations. The determined value of the apparent Michaelis-Menten constant was 0.045 mmol dm(-3) which is significantly lower than that of free enzyme indicating enhanced enzyme efficiency when it is immobilized into electroconducting polymer matrix.",
publisher = "Esg, Belgrade",
journal = "International Journal of Electrochemical Science",
title = "Polypyrrole-based Enzyme Electrode with Immobilized Glucose Oxidase for Electrochemical Determination of Glucose",
volume = "11",
number = "2",
pages = "1152-1161",
url = "https://hdl.handle.net/21.15107/rcub_dais_15979"
}

Jugović, B., Grgur, B. N., Antov, M., Knežević-Jugović, Z., Stevanović, J.,& Gvozdenović, M. M.. (2016). Polypyrrole-based Enzyme Electrode with Immobilized Glucose Oxidase for Electrochemical Determination of Glucose. in International Journal of Electrochemical Science
Esg, Belgrade., 11(2), 1152-1161.
https://hdl.handle.net/21.15107/rcub_dais_15979

Jugović B, Grgur BN, Antov M, Knežević-Jugović Z, Stevanović J, Gvozdenović MM. Polypyrrole-based Enzyme Electrode with Immobilized Glucose Oxidase for Electrochemical Determination of Glucose. in International Journal of Electrochemical Science. 2016;11(2):1152-1161.
https://hdl.handle.net/21.15107/rcub_dais_15979 .

Jugović, Branimir, Grgur, Branimir N., Antov, Mirjana, Knežević-Jugović, Zorica, Stevanović, Jasmina, Gvozdenović, Milica M., "Polypyrrole-based Enzyme Electrode with Immobilized Glucose Oxidase for Electrochemical Determination of Glucose" in International Journal of Electrochemical Science, 11, no. 2 (2016):1152-1161,
https://hdl.handle.net/21.15107/rcub_dais_15979 .

TY  - JOUR
AU  - Tomković, Tanja
AU  - Radovanović, Filip
AU  - Nastasović, Aleksandra
AU  - Vasiljević-Radović, Dana
AU  - Markovic, Jelena
AU  - Grgur, Branimir N.
AU  - Onjia, Antonije E.
PY  - 2015
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1748
AB  - Asymmetric polyethersulfone membranes with submicron particles comprising crosslinked poly(glycidyl methacrylate-co-2-acrylamido-2-methylpropane sulfonic acid) were prepared by a combination of a traditional liquid phase inversion process for making membranes with photopolymerization and crosslinking of functional monomers included in the casting solution. Scanning electron microscope images of the membrane cross-section revealed a hybrid structure with an interconnected network of submicron particles embedded within the porous polyethersulfone support. Permeation of toluidine blue solutions through non-functionalized membranes showed a dramatic effect of 2-acrylamido-2-methylpropane sulfonic acid concentration in the casting solution on the dynamic adsorption performance. The epoxide groups present in glycidyl methacrylate copolymer were transformed into amine functionalities by ring opening under alkaline conditions. Permeation of dilute Cu2+ solutions through functionalized membranes demonstrated that the plate height for some of these membranes was an order of magnitude smaller than for commercial particle-filled membranes used in solid phase extraction.
PB  - Oxford : Pergamon-Elsevier Science Ltd
T2  - European Polymer Journal
T1  - Solid phase extraction membranes with submicron multifunctional adsorbent particles
VL  - 63
SP  - 90
EP  - 100
DO  - 10.1016/j.eurpolymj.2014.12.015
ER  - 

@article{
author = "Tomković, Tanja and Radovanović, Filip and Nastasović, Aleksandra and Vasiljević-Radović, Dana and Markovic, Jelena and Grgur, Branimir N. and Onjia, Antonije E.",
year = "2015",
abstract = "Asymmetric polyethersulfone membranes with submicron particles comprising crosslinked poly(glycidyl methacrylate-co-2-acrylamido-2-methylpropane sulfonic acid) were prepared by a combination of a traditional liquid phase inversion process for making membranes with photopolymerization and crosslinking of functional monomers included in the casting solution. Scanning electron microscope images of the membrane cross-section revealed a hybrid structure with an interconnected network of submicron particles embedded within the porous polyethersulfone support. Permeation of toluidine blue solutions through non-functionalized membranes showed a dramatic effect of 2-acrylamido-2-methylpropane sulfonic acid concentration in the casting solution on the dynamic adsorption performance. The epoxide groups present in glycidyl methacrylate copolymer were transformed into amine functionalities by ring opening under alkaline conditions. Permeation of dilute Cu2+ solutions through functionalized membranes demonstrated that the plate height for some of these membranes was an order of magnitude smaller than for commercial particle-filled membranes used in solid phase extraction.",
publisher = "Oxford : Pergamon-Elsevier Science Ltd",
journal = "European Polymer Journal",
title = "Solid phase extraction membranes with submicron multifunctional adsorbent particles",
volume = "63",
pages = "90-100",
doi = "10.1016/j.eurpolymj.2014.12.015"
}

Tomković, T., Radovanović, F., Nastasović, A., Vasiljević-Radović, D., Markovic, J., Grgur, B. N.,& Onjia, A. E.. (2015). Solid phase extraction membranes with submicron multifunctional adsorbent particles. in European Polymer Journal
Oxford : Pergamon-Elsevier Science Ltd., 63, 90-100.
https://doi.org/10.1016/j.eurpolymj.2014.12.015

Tomković T, Radovanović F, Nastasović A, Vasiljević-Radović D, Markovic J, Grgur BN, Onjia AE. Solid phase extraction membranes with submicron multifunctional adsorbent particles. in European Polymer Journal. 2015;63:90-100.
doi:10.1016/j.eurpolymj.2014.12.015 .

Tomković, Tanja, Radovanović, Filip, Nastasović, Aleksandra, Vasiljević-Radović, Dana, Markovic, Jelena, Grgur, Branimir N., Onjia, Antonije E., "Solid phase extraction membranes with submicron multifunctional adsorbent particles" in European Polymer Journal, 63 (2015):90-100,
https://doi.org/10.1016/j.eurpolymj.2014.12.015 . .

TY  - JOUR
AU  - Popović, Nataša
AU  - Jugović, Branimir
AU  - Jokić, Bojan
AU  - Knežević-Jugović, Zorica
AU  - Stevanović, Jasmina
AU  - Grgur, Branimir N.
AU  - Gvozdenović, Milica M.
PY  - 2015
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1743
AB  - Electrochemical formation of polyaniline (PANI) modified electrode was performed galvanostatically from aqueous solution of 1.0 mol dm(-3) HCl containing 0.2 mol dm(-3) aniline at current densities ranging from 0.5-3.0 mA cm(-2). The morphology of PANI electrode consisted of highly developed nanofibrous network with electrocatalytic features towards oxidation of ascorbic acid, reflected in increase of the peak current similar to 2.5 times and shift of the oxidation potential by 0.32 V to less positive values. Response of PANI modified electrode was obtained from anodic LSV curves. Current peak potentials decreased with increase of pH with slope of similar to 32 mV pH(-1), indicating two electron charge transfer process with liberation of one proton characteristic of an electrochemical reaction followed by a chemical step.
PB  - Electrochemical Science Group
T2  - International Journal of Electrochemical Science
T1  - Electrochemical Template-Free Synthesis of Nanofibrous Polyaniline Modified Electrode for Ascorbic Acid Determination
VL  - 10
IS  - 2
SP  - 1208
EP  - 1220
UR  - https://hdl.handle.net/21.15107/rcub_dais_3543
ER  - 

@article{
author = "Popović, Nataša and Jugović, Branimir and Jokić, Bojan and Knežević-Jugović, Zorica and Stevanović, Jasmina and Grgur, Branimir N. and Gvozdenović, Milica M.",
year = "2015",
abstract = "Electrochemical formation of polyaniline (PANI) modified electrode was performed galvanostatically from aqueous solution of 1.0 mol dm(-3) HCl containing 0.2 mol dm(-3) aniline at current densities ranging from 0.5-3.0 mA cm(-2). The morphology of PANI electrode consisted of highly developed nanofibrous network with electrocatalytic features towards oxidation of ascorbic acid, reflected in increase of the peak current similar to 2.5 times and shift of the oxidation potential by 0.32 V to less positive values. Response of PANI modified electrode was obtained from anodic LSV curves. Current peak potentials decreased with increase of pH with slope of similar to 32 mV pH(-1), indicating two electron charge transfer process with liberation of one proton characteristic of an electrochemical reaction followed by a chemical step.",
publisher = "Electrochemical Science Group",
journal = "International Journal of Electrochemical Science",
title = "Electrochemical Template-Free Synthesis of Nanofibrous Polyaniline Modified Electrode for Ascorbic Acid Determination",
volume = "10",
number = "2",
pages = "1208-1220",
url = "https://hdl.handle.net/21.15107/rcub_dais_3543"
}

Popović, N., Jugović, B., Jokić, B., Knežević-Jugović, Z., Stevanović, J., Grgur, B. N.,& Gvozdenović, M. M.. (2015). Electrochemical Template-Free Synthesis of Nanofibrous Polyaniline Modified Electrode for Ascorbic Acid Determination. in International Journal of Electrochemical Science
Electrochemical Science Group., 10(2), 1208-1220.
https://hdl.handle.net/21.15107/rcub_dais_3543

Popović N, Jugović B, Jokić B, Knežević-Jugović Z, Stevanović J, Grgur BN, Gvozdenović MM. Electrochemical Template-Free Synthesis of Nanofibrous Polyaniline Modified Electrode for Ascorbic Acid Determination. in International Journal of Electrochemical Science. 2015;10(2):1208-1220.
https://hdl.handle.net/21.15107/rcub_dais_3543 .

Popović, Nataša, Jugović, Branimir, Jokić, Bojan, Knežević-Jugović, Zorica, Stevanović, Jasmina, Grgur, Branimir N., Gvozdenović, Milica M., "Electrochemical Template-Free Synthesis of Nanofibrous Polyaniline Modified Electrode for Ascorbic Acid Determination" in International Journal of Electrochemical Science, 10, no. 2 (2015):1208-1220,
https://hdl.handle.net/21.15107/rcub_dais_3543 .

TY  - JOUR
AU  - Radoman, Tijana S
AU  - Džunuzović, Jasna
AU  - Jeremić, Katarina B.
AU  - Grgur, Branimir N.
AU  - Milicevic, Dejan S
AU  - Popović, Ivanka G.
AU  - Džunuzović, Enis S.
PY  - 2014
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1552
AB  - Epoxy resin/titanium dioxide (epoxy/TiO2) nanocomposites were obtained by incorporation of TiO2 nanoparticles surface modified with gallic acid esters in epoxy resin. TiO2 nanoparticles were obtained by acid catalyzed hydrolysis of titanium isopropoxide and their structural characterization was performed by X-ray diffraction and transmission electron microscopy. Three gallic acid esters, having different hydrophobic part, were used for surface modification of the synthesized TiO2 nanoparticles: propyl, hexyl and lauryl gallate. The gallate chemisorption onto surface of TiO2 nanoparticles was confirmed by Fourier transform infrared and ultraviolet-visible spectroscopy, while the amount of surface-bonded gallates was determined using thermogravimetric analysis. The influence of the surface modified TiO2 nanoparticles, as well as the length of hydrophobic part of the gallate used for surface modification of TiO2 nanoparticles, on glass transition temperature, barrier, dielectric and anticorrosive properties of epoxy resin was investigated by differential scanning calorimetry, water vapor transmission test, dielectric spectroscopy, electrochemical impedance spectroscopy and polarization measurements. Incorporation of surface modified TiO2 nanoparticles in epoxy resin caused increase of glass transition temperature and decrease of the water vapor permeability of epoxy resin. The water vapor transmission rate of epoxy/TiO2 nanocomposites was reduced with increasing hydrophobic part chain length of gallate ligand. Dielectric constant of examined nanocomposites was influenced by gallate used for the modification of TiO2 nanoparticles. The nanocomposites have better anticorrosive properties than pure epoxy resin, because the surface modified TiO2 nanoparticles react as oxygen scavengers, which inhibit steel corrosion by cathodic mechanism.
PB  - Elsevier Sci Ltd, Oxford
T2  - Materials & Design
T1  - Improvement of epoxy resin properties by incorporation of TiO2 nanoparticles surface modified with gallic acid esters
VL  - 62
SP  - 158
EP  - 167
DO  - 10.1016/j.matdes.2014.05.015
ER  - 

@article{
author = "Radoman, Tijana S and Džunuzović, Jasna and Jeremić, Katarina B. and Grgur, Branimir N. and Milicevic, Dejan S and Popović, Ivanka G. and Džunuzović, Enis S.",
year = "2014",
abstract = "Epoxy resin/titanium dioxide (epoxy/TiO2) nanocomposites were obtained by incorporation of TiO2 nanoparticles surface modified with gallic acid esters in epoxy resin. TiO2 nanoparticles were obtained by acid catalyzed hydrolysis of titanium isopropoxide and their structural characterization was performed by X-ray diffraction and transmission electron microscopy. Three gallic acid esters, having different hydrophobic part, were used for surface modification of the synthesized TiO2 nanoparticles: propyl, hexyl and lauryl gallate. The gallate chemisorption onto surface of TiO2 nanoparticles was confirmed by Fourier transform infrared and ultraviolet-visible spectroscopy, while the amount of surface-bonded gallates was determined using thermogravimetric analysis. The influence of the surface modified TiO2 nanoparticles, as well as the length of hydrophobic part of the gallate used for surface modification of TiO2 nanoparticles, on glass transition temperature, barrier, dielectric and anticorrosive properties of epoxy resin was investigated by differential scanning calorimetry, water vapor transmission test, dielectric spectroscopy, electrochemical impedance spectroscopy and polarization measurements. Incorporation of surface modified TiO2 nanoparticles in epoxy resin caused increase of glass transition temperature and decrease of the water vapor permeability of epoxy resin. The water vapor transmission rate of epoxy/TiO2 nanocomposites was reduced with increasing hydrophobic part chain length of gallate ligand. Dielectric constant of examined nanocomposites was influenced by gallate used for the modification of TiO2 nanoparticles. The nanocomposites have better anticorrosive properties than pure epoxy resin, because the surface modified TiO2 nanoparticles react as oxygen scavengers, which inhibit steel corrosion by cathodic mechanism.",
publisher = "Elsevier Sci Ltd, Oxford",
journal = "Materials & Design",
title = "Improvement of epoxy resin properties by incorporation of TiO2 nanoparticles surface modified with gallic acid esters",
volume = "62",
pages = "158-167",
doi = "10.1016/j.matdes.2014.05.015"
}

Radoman, T. S., Džunuzović, J., Jeremić, K. B., Grgur, B. N., Milicevic, D. S., Popović, I. G.,& Džunuzović, E. S.. (2014). Improvement of epoxy resin properties by incorporation of TiO2 nanoparticles surface modified with gallic acid esters. in Materials & Design
Elsevier Sci Ltd, Oxford., 62, 158-167.
https://doi.org/10.1016/j.matdes.2014.05.015

Radoman TS, Džunuzović J, Jeremić KB, Grgur BN, Milicevic DS, Popović IG, Džunuzović ES. Improvement of epoxy resin properties by incorporation of TiO2 nanoparticles surface modified with gallic acid esters. in Materials & Design. 2014;62:158-167.
doi:10.1016/j.matdes.2014.05.015 .

Radoman, Tijana S, Džunuzović, Jasna, Jeremić, Katarina B., Grgur, Branimir N., Milicevic, Dejan S, Popović, Ivanka G., Džunuzović, Enis S., "Improvement of epoxy resin properties by incorporation of TiO2 nanoparticles surface modified with gallic acid esters" in Materials & Design, 62 (2014):158-167,
https://doi.org/10.1016/j.matdes.2014.05.015 . .

TY  - JOUR
AU  - Gvozdenović, Milica M.
AU  - Jugović, Branimir
AU  - Stevanović, Jasmina
AU  - Grgur, Branimir N.
PY  - 2014
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1455
AB  - Electroconducting polymers from the group of synthetic metals are extensively investigated due to numerous properties perspective in practical application. These materials may be synthesized by both chemical and electrochemical procedures. Chemical synthesis is suitable when bulk quantities of the polymer are necessary and up to date it presents dominant commercial method of producing electroconducting polymers. Nevertheless, the electrochemical synthesis has its advantages; it avoids usage of oxidants since conducting polymeric material is obtained at anode upon application of positive potential, leading to increased purity. On the other hand, since the polymer is deposited onto electrode, further electrochemical characterization is facilitated. Owing to actuality of the research in the field, this text aims to describe important aspects of electrochemical synthesis of electroconducting polymers, with special emphasis to polyaniline and polypyrrole.
AB  - Tradicionalno shvatanje o polimerima kao odličnim izolatorima izmenjeno je sedamdesetih godina prošlog veka kada su naučnici uspeli da sintetizuju poiliacetilen čija je provodljivost bila bliska metalnoj. Ova činjenica ukazala je na novo svojstvo polimernih materijala i lansirala potpuno novo multidisciplinarno naučno polje, popularno nazvano, sintetički metali. Iako je danas pojmom elektroprovodnih polimera obuhvaćena velika grupa jedinjenja koja su klasifikovana prema prirodi prenosioca naelektrisanja, naziv elektroprovodni polimeri se najčešće koristi u literaturi upravo za polimerne materijala iz grupe sintetičkih metala koji poseduju elektronsku provodljivost kao posledicu specifičnosti molekulske strukture. Pored zahteva molekulske structure, koja podrazumeva konjugovani sistem dvostrukih veza, za provodljivost elektroprovodnih polimera neophodno je dopovanje. Termin dopovanje, iako preuzet iz terminologije klasičnih neorganskih poluprovodnika, podrazumeva u mnogome drugačiji proces. Dopovanje elektroprovodnih polimera podrazumeva oksidaciju tokom koje se, u cilju održavanja elektroneutralnosti polimernog lanca, uvodi stehiometrijska količina jona (anjona). Terminom dopovanje obuhvaćena je i protonacija polimernog lanca kiselinom, u slučaju polianilina, a nedavno je potvrđena i u slučaju polipirola. Kako je, na ovaj način, uvedena velika količina jona izmenjenja je polazna struktura elektroprovodnog polimera, tako da svojstva nastalog materijala zavise u velikoj meri od svojstava dopanta. Iako su na početku razvoja ove oblasti, elektroprovodni polimeri bili sintetizovani hemijskim postupcima, sticanjem uvida u mehanizam hemijske sinteze koja podrazumeva oksidativnu radikalnu polimerizaciju, postalo je jasno da se ovi materijali mogu dobiti i elektrohemijskim postupcima. Elektrohemijska sinteza ima prednosti, pošto se polimer dobija oksidacijom na elektrodama (anodama), čime je izbegnuta upotreba oksidacinog sredstva i omogućena veća čistoća proizvoda. Sa druge strane, elektroprovodni polimer je u većini slučajeva dobijen u obliku prevlake na elektrodi, pa je njegova dalja karakterizacija elektrohemijskim tenikama olakšana. Interesovanje za oblst sinteze elektroprovodnih polimera ne jenjava, pa je ovaj tekst posvećen osnovnim principima elektrohemijskih postupaka sinteze sa posebnim osvrtom na najpopularnije elektroprovodne polimere, polianilin i polipirol.
PB  - Association of Chemical Engineers of Serbia
T2  - Hemijska industrija
T1  - Electrochemical synthesis of electroconducting polymers
T1  - Elektrohemijska sinteza elektroprovodnih polimera
VL  - 68
IS  - 6
SP  - 673
EP  - 684
DO  - 10.2298/HEMIND131122008G
ER  - 

@article{
author = "Gvozdenović, Milica M. and Jugović, Branimir and Stevanović, Jasmina and Grgur, Branimir N.",
year = "2014",
abstract = "Electroconducting polymers from the group of synthetic metals are extensively investigated due to numerous properties perspective in practical application. These materials may be synthesized by both chemical and electrochemical procedures. Chemical synthesis is suitable when bulk quantities of the polymer are necessary and up to date it presents dominant commercial method of producing electroconducting polymers. Nevertheless, the electrochemical synthesis has its advantages; it avoids usage of oxidants since conducting polymeric material is obtained at anode upon application of positive potential, leading to increased purity. On the other hand, since the polymer is deposited onto electrode, further electrochemical characterization is facilitated. Owing to actuality of the research in the field, this text aims to describe important aspects of electrochemical synthesis of electroconducting polymers, with special emphasis to polyaniline and polypyrrole., Tradicionalno shvatanje o polimerima kao odličnim izolatorima izmenjeno je sedamdesetih godina prošlog veka kada su naučnici uspeli da sintetizuju poiliacetilen čija je provodljivost bila bliska metalnoj. Ova činjenica ukazala je na novo svojstvo polimernih materijala i lansirala potpuno novo multidisciplinarno naučno polje, popularno nazvano, sintetički metali. Iako je danas pojmom elektroprovodnih polimera obuhvaćena velika grupa jedinjenja koja su klasifikovana prema prirodi prenosioca naelektrisanja, naziv elektroprovodni polimeri se najčešće koristi u literaturi upravo za polimerne materijala iz grupe sintetičkih metala koji poseduju elektronsku provodljivost kao posledicu specifičnosti molekulske strukture. Pored zahteva molekulske structure, koja podrazumeva konjugovani sistem dvostrukih veza, za provodljivost elektroprovodnih polimera neophodno je dopovanje. Termin dopovanje, iako preuzet iz terminologije klasičnih neorganskih poluprovodnika, podrazumeva u mnogome drugačiji proces. Dopovanje elektroprovodnih polimera podrazumeva oksidaciju tokom koje se, u cilju održavanja elektroneutralnosti polimernog lanca, uvodi stehiometrijska količina jona (anjona). Terminom dopovanje obuhvaćena je i protonacija polimernog lanca kiselinom, u slučaju polianilina, a nedavno je potvrđena i u slučaju polipirola. Kako je, na ovaj način, uvedena velika količina jona izmenjenja je polazna struktura elektroprovodnog polimera, tako da svojstva nastalog materijala zavise u velikoj meri od svojstava dopanta. Iako su na početku razvoja ove oblasti, elektroprovodni polimeri bili sintetizovani hemijskim postupcima, sticanjem uvida u mehanizam hemijske sinteze koja podrazumeva oksidativnu radikalnu polimerizaciju, postalo je jasno da se ovi materijali mogu dobiti i elektrohemijskim postupcima. Elektrohemijska sinteza ima prednosti, pošto se polimer dobija oksidacijom na elektrodama (anodama), čime je izbegnuta upotreba oksidacinog sredstva i omogućena veća čistoća proizvoda. Sa druge strane, elektroprovodni polimer je u većini slučajeva dobijen u obliku prevlake na elektrodi, pa je njegova dalja karakterizacija elektrohemijskim tenikama olakšana. Interesovanje za oblst sinteze elektroprovodnih polimera ne jenjava, pa je ovaj tekst posvećen osnovnim principima elektrohemijskih postupaka sinteze sa posebnim osvrtom na najpopularnije elektroprovodne polimere, polianilin i polipirol.",
publisher = "Association of Chemical Engineers of Serbia",
journal = "Hemijska industrija",
title = "Electrochemical synthesis of electroconducting polymers, Elektrohemijska sinteza elektroprovodnih polimera",
volume = "68",
number = "6",
pages = "673-684",
doi = "10.2298/HEMIND131122008G"
}

Gvozdenović, M. M., Jugović, B., Stevanović, J.,& Grgur, B. N.. (2014). Electrochemical synthesis of electroconducting polymers. in Hemijska industrija
Association of Chemical Engineers of Serbia., 68(6), 673-684.
https://doi.org/10.2298/HEMIND131122008G

Gvozdenović MM, Jugović B, Stevanović J, Grgur BN. Electrochemical synthesis of electroconducting polymers. in Hemijska industrija. 2014;68(6):673-684.
doi:10.2298/HEMIND131122008G .

Gvozdenović, Milica M., Jugović, Branimir, Stevanović, Jasmina, Grgur, Branimir N., "Electrochemical synthesis of electroconducting polymers" in Hemijska industrija, 68, no. 6 (2014):673-684,
https://doi.org/10.2298/HEMIND131122008G . .

TY  - CONF
AU  - Gvozdenović, Milica M.
AU  - Popović, N.
AU  - Stevanović, Jasmina
AU  - Grgur, Branimir N.
AU  - Trišović, Tomislav
AU  - Jugović, Branimir
PY  - 2014
UR  - http://dais.sanu.ac.rs/123456789/587
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2621
AB  - Electroconducting polymers are promising materials to be used in various fields including: batteries, capacitors, electronic devices, corrosion, biosensors and sensors[1,6]. Polyaniline is probably the most investigated electroconducting polymer, due to low cost monomer, conductivity, environmental stability. Polyaniline can be obtained by chemical or electrochemical oxidative polymerization of aniline. Electrochemical synthesis is performed in anodic process directly from acidic aqueous electrolyte containing aniline. Polyaniline can be used as electrode material for electrochemical determination of ascorbic acid based on electrocatalytic oxidation of ascorbic acid.
PB  - Tatranské Matliare : Slovak Society of Chemical Engineering
C3  - Proceedings of the 41st International Conference of Slovak Society of Chemical Engineering
T1  - Electrochemical determination of ascorbic acid using electrochemically deposited polyaniline
SP  - 654
EP  - 657
UR  - https://hdl.handle.net/21.15107/rcub_dais_587
ER  - 

@conference{
author = "Gvozdenović, Milica M. and Popović, N. and Stevanović, Jasmina and Grgur, Branimir N. and Trišović, Tomislav and Jugović, Branimir",
year = "2014",
abstract = "Electroconducting polymers are promising materials to be used in various fields including: batteries, capacitors, electronic devices, corrosion, biosensors and sensors[1,6]. Polyaniline is probably the most investigated electroconducting polymer, due to low cost monomer, conductivity, environmental stability. Polyaniline can be obtained by chemical or electrochemical oxidative polymerization of aniline. Electrochemical synthesis is performed in anodic process directly from acidic aqueous electrolyte containing aniline. Polyaniline can be used as electrode material for electrochemical determination of ascorbic acid based on electrocatalytic oxidation of ascorbic acid.",
publisher = "Tatranské Matliare : Slovak Society of Chemical Engineering",
journal = "Proceedings of the 41st International Conference of Slovak Society of Chemical Engineering",
title = "Electrochemical determination of ascorbic acid using electrochemically deposited polyaniline",
pages = "654-657",
url = "https://hdl.handle.net/21.15107/rcub_dais_587"
}

Gvozdenović, M. M., Popović, N., Stevanović, J., Grgur, B. N., Trišović, T.,& Jugović, B.. (2014). Electrochemical determination of ascorbic acid using electrochemically deposited polyaniline. in Proceedings of the 41st International Conference of Slovak Society of Chemical Engineering
Tatranské Matliare : Slovak Society of Chemical Engineering., 654-657.
https://hdl.handle.net/21.15107/rcub_dais_587

Gvozdenović MM, Popović N, Stevanović J, Grgur BN, Trišović T, Jugović B. Electrochemical determination of ascorbic acid using electrochemically deposited polyaniline. in Proceedings of the 41st International Conference of Slovak Society of Chemical Engineering. 2014;:654-657.
https://hdl.handle.net/21.15107/rcub_dais_587 .

Gvozdenović, Milica M., Popović, N., Stevanović, Jasmina, Grgur, Branimir N., Trišović, Tomislav, Jugović, Branimir, "Electrochemical determination of ascorbic acid using electrochemically deposited polyaniline" in Proceedings of the 41st International Conference of Slovak Society of Chemical Engineering (2014):654-657,
https://hdl.handle.net/21.15107/rcub_dais_587 .

TY  - JOUR
AU  - Smiljanić, Milutin
AU  - Srejić, Irina
AU  - Grgur, Branimir N.
AU  - Rakočević, Zlatko Lj.
AU  - Štrbac, Svetlana
PY  - 2013
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1280
AB  - Hydrogen evolution reaction (HER) was studied on Pd/Au(1 1 1) bimetallic surfaces in alkaline solution. Au(1 1 1) was modified by palladium nanoislands spontaneously deposited using PdSO4 center dot 2H(2)O and PdCl2 salts. As revealed from both surface topography Atomic Force Microscopy (AFM) and phase AFM images, for the same deposition conditions, the obtained Pd/Au(1 1 1) nanostructures differ depending on the counter anion in the depositing palladium salt. These differences are reflected on their catalytic activity toward HER, which occurs between the potentials for pure consisting metals. HER proceeded with the same mechanism, but it is shifted to more positive potentials for Pd/Au(1 1 1) nanostructures obtained using PdCl2 salt with respect to ones obtained using PdSO4 salt. Better catalytic activity of Pd/Au(1 1 1) nanostructures obtained using PdCl2 salt can be explained by their surface structure consisting of smaller and thinner Pd nanoislands, preferentially deposited at steps, which provides more Pd and Pd/Au sites suitable for hydrogen evolution reaction.
PB  - Oxford : Pergamon-Elsevier Science Ltd
T2  - Electrochimica Acta
T1  - Catalysis of hydrogen evolution on different Pd/Au(111) nanostructures in alkaline solution
VL  - 88
SP  - 589
EP  - 596
DO  - 10.1016/j.electacta.2012.10.128
ER  - 

@article{
author = "Smiljanić, Milutin and Srejić, Irina and Grgur, Branimir N. and Rakočević, Zlatko Lj. and Štrbac, Svetlana",
year = "2013",
abstract = "Hydrogen evolution reaction (HER) was studied on Pd/Au(1 1 1) bimetallic surfaces in alkaline solution. Au(1 1 1) was modified by palladium nanoislands spontaneously deposited using PdSO4 center dot 2H(2)O and PdCl2 salts. As revealed from both surface topography Atomic Force Microscopy (AFM) and phase AFM images, for the same deposition conditions, the obtained Pd/Au(1 1 1) nanostructures differ depending on the counter anion in the depositing palladium salt. These differences are reflected on their catalytic activity toward HER, which occurs between the potentials for pure consisting metals. HER proceeded with the same mechanism, but it is shifted to more positive potentials for Pd/Au(1 1 1) nanostructures obtained using PdCl2 salt with respect to ones obtained using PdSO4 salt. Better catalytic activity of Pd/Au(1 1 1) nanostructures obtained using PdCl2 salt can be explained by their surface structure consisting of smaller and thinner Pd nanoislands, preferentially deposited at steps, which provides more Pd and Pd/Au sites suitable for hydrogen evolution reaction.",
publisher = "Oxford : Pergamon-Elsevier Science Ltd",
journal = "Electrochimica Acta",
title = "Catalysis of hydrogen evolution on different Pd/Au(111) nanostructures in alkaline solution",
volume = "88",
pages = "589-596",
doi = "10.1016/j.electacta.2012.10.128"
}

Smiljanić, M., Srejić, I., Grgur, B. N., Rakočević, Z. Lj.,& Štrbac, S.. (2013). Catalysis of hydrogen evolution on different Pd/Au(111) nanostructures in alkaline solution. in Electrochimica Acta
Oxford : Pergamon-Elsevier Science Ltd., 88, 589-596.
https://doi.org/10.1016/j.electacta.2012.10.128

Smiljanić M, Srejić I, Grgur BN, Rakočević ZL, Štrbac S. Catalysis of hydrogen evolution on different Pd/Au(111) nanostructures in alkaline solution. in Electrochimica Acta. 2013;88:589-596.
doi:10.1016/j.electacta.2012.10.128 .

Smiljanić, Milutin, Srejić, Irina, Grgur, Branimir N., Rakočević, Zlatko Lj., Štrbac, Svetlana, "Catalysis of hydrogen evolution on different Pd/Au(111) nanostructures in alkaline solution" in Electrochimica Acta, 88 (2013):589-596,
https://doi.org/10.1016/j.electacta.2012.10.128 . .

TY  - JOUR
AU  - Smiljanić, Milutin
AU  - Srejić, Irina
AU  - Grgur, Branimir N.
AU  - Rakočević, Zlatko Lj.
AU  - Štrbac, Svetlana
PY  - 2013
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1287
AB  - Pronounced catalysis of hydrogen evolution reaction (HER) by rhodium nanoislands spontaneously deposited on Au(111) has been observed. Different Rh/Au(111) nanostructures were characterized ex situ by both height and phase imaging AFM. The most pronounced catalytic activity for HER in 0.5 M H2SO4 was obtained for 50% Rh coverage. This is ascribed to the suitable size of Rh nanoislands and to the electronic modification of Rh deposit by Au(111) substrate.
PB  - Elsevier Science Inc, New York
T2  - Electrochemistry Communications
T1  - Hydrogen evolution on Au(111) catalyzed by rhodium nanoislands
VL  - 28
SP  - 37
EP  - 39
DO  - 10.1016/j.elecom.2012.12.009
ER  - 

@article{
author = "Smiljanić, Milutin and Srejić, Irina and Grgur, Branimir N. and Rakočević, Zlatko Lj. and Štrbac, Svetlana",
year = "2013",
abstract = "Pronounced catalysis of hydrogen evolution reaction (HER) by rhodium nanoislands spontaneously deposited on Au(111) has been observed. Different Rh/Au(111) nanostructures were characterized ex situ by both height and phase imaging AFM. The most pronounced catalytic activity for HER in 0.5 M H2SO4 was obtained for 50% Rh coverage. This is ascribed to the suitable size of Rh nanoislands and to the electronic modification of Rh deposit by Au(111) substrate.",
publisher = "Elsevier Science Inc, New York",
journal = "Electrochemistry Communications",
title = "Hydrogen evolution on Au(111) catalyzed by rhodium nanoislands",
volume = "28",
pages = "37-39",
doi = "10.1016/j.elecom.2012.12.009"
}

Smiljanić, M., Srejić, I., Grgur, B. N., Rakočević, Z. Lj.,& Štrbac, S.. (2013). Hydrogen evolution on Au(111) catalyzed by rhodium nanoislands. in Electrochemistry Communications
Elsevier Science Inc, New York., 28, 37-39.
https://doi.org/10.1016/j.elecom.2012.12.009

Smiljanić M, Srejić I, Grgur BN, Rakočević ZL, Štrbac S. Hydrogen evolution on Au(111) catalyzed by rhodium nanoislands. in Electrochemistry Communications. 2013;28:37-39.
doi:10.1016/j.elecom.2012.12.009 .

Smiljanić, Milutin, Srejić, Irina, Grgur, Branimir N., Rakočević, Zlatko Lj., Štrbac, Svetlana, "Hydrogen evolution on Au(111) catalyzed by rhodium nanoislands" in Electrochemistry Communications, 28 (2013):37-39,
https://doi.org/10.1016/j.elecom.2012.12.009 . .

TY  - JOUR
AU  - Mijin, Dušan
AU  - Avramov Ivić, Milka
AU  - Onjia, Antonije E.
AU  - Grgur, Branimir N.
PY  - 2012
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1124
AB  - Reaction of the indirect electrochemical decolorization of cationic textile dye CI Basic Yellow 28 with electrochemically generated "active chlorine" has been studied, using UV-Vis spectrophotometry, ion chromatography, organic carbon analysis, and cyclic voltammetry. Decolorization has been investigated on Ti/PtOx anode for different currents in the range of 50-200 mA, sodium chloride concentration in the range from 5 to 25 g dm(-3), and dye concentration from 10 to 70 mg dm(-3). The optimum electrolysis conditions and possible active species have been suggested.
PB  - Elsevier Science Sa, Lausanne
T2  - Chemical Engineering Journal
T1  - Decolorization of textile dye CI Basic Yellow 28 with electrochemically generated active chlorine
VL  - 204
SP  - 151
EP  - 157
DO  - 10.1016/j.cej.2012.07.091
ER  - 

@article{
author = "Mijin, Dušan and Avramov Ivić, Milka and Onjia, Antonije E. and Grgur, Branimir N.",
year = "2012",
abstract = "Reaction of the indirect electrochemical decolorization of cationic textile dye CI Basic Yellow 28 with electrochemically generated "active chlorine" has been studied, using UV-Vis spectrophotometry, ion chromatography, organic carbon analysis, and cyclic voltammetry. Decolorization has been investigated on Ti/PtOx anode for different currents in the range of 50-200 mA, sodium chloride concentration in the range from 5 to 25 g dm(-3), and dye concentration from 10 to 70 mg dm(-3). The optimum electrolysis conditions and possible active species have been suggested.",
publisher = "Elsevier Science Sa, Lausanne",
journal = "Chemical Engineering Journal",
title = "Decolorization of textile dye CI Basic Yellow 28 with electrochemically generated active chlorine",
volume = "204",
pages = "151-157",
doi = "10.1016/j.cej.2012.07.091"
}

Mijin, D., Avramov Ivić, M., Onjia, A. E.,& Grgur, B. N.. (2012). Decolorization of textile dye CI Basic Yellow 28 with electrochemically generated active chlorine. in Chemical Engineering Journal
Elsevier Science Sa, Lausanne., 204, 151-157.
https://doi.org/10.1016/j.cej.2012.07.091

Mijin D, Avramov Ivić M, Onjia AE, Grgur BN. Decolorization of textile dye CI Basic Yellow 28 with electrochemically generated active chlorine. in Chemical Engineering Journal. 2012;204:151-157.
doi:10.1016/j.cej.2012.07.091 .

Mijin, Dušan, Avramov Ivić, Milka, Onjia, Antonije E., Grgur, Branimir N., "Decolorization of textile dye CI Basic Yellow 28 with electrochemically generated active chlorine" in Chemical Engineering Journal, 204 (2012):151-157,
https://doi.org/10.1016/j.cej.2012.07.091 . .

TY  - JOUR
AU  - Srejić, Irina
AU  - Smiljanić, Milutin
AU  - Grgur, Branimir N.
AU  - Rakočević, Zlatko Lj.
AU  - Štrbac, Svetlana
PY  - 2012
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1015
AB  - Oxygen reduction reaction (ORR) was studied on polycrystalline gold, Au(poly), modified by nanosized palladium islands in 0.1 M HClO4 solution using rotating disc electrode technique. Paladium was spontaneously deposited from 1 mM PdSO4 center dot 2H(2)O + 0.5 M H2SO4 solution for various deposition times at a submonolayer coverage. Topography of obtained Pd/Au(poly) surfaces was observed by tapping mode atomic force microscopy (AFM), while chemical surface composition changes were detected by simultaneously performed phase AFM. Deposited Pd islands were nonuniform in size and randomly distributed over the gold substrate. Size and number of Pd islands increase with the increase of the deposition time, and consequently surface coverage increases too. Deposited Pd was also identified by the changes in cyclic voltammetry (CV) profiles from which an active surface area was estimated. Obtained Pd/Au(poly) surfaces have shown a significant catalytic activity towards oxygen reduction reaction which increases with the increase of Pd islands coverage. The initial potential of ORR was shifted positively, while reaction pathway changes from 2e-reduction on pure gold to 4e-reduction on Pd modified gold. Additionally, obtained Pd/Au(poly) surfaces have shown a significant activity towards hydrogen peroxide reduction (HPRR), which appear as an intermediate during ORR. This supports the assumption that ORR on Pd/Au(poly) occurs partly through 4e-series reduction pathway, the fraction of which increases with the increase of Pd coverage.
PB  - Oxford : Pergamon-Elsevier Science Ltd
T2  - Electrochimica Acta
T1  - Catalysis of oxygen reduction on Au modified by Pd nanoislands in perchloric acid solution
VL  - 64
SP  - 140
EP  - 146
DO  - 10.1016/j.electacta.2011.12.130
ER  - 

@article{
author = "Srejić, Irina and Smiljanić, Milutin and Grgur, Branimir N. and Rakočević, Zlatko Lj. and Štrbac, Svetlana",
year = "2012",
abstract = "Oxygen reduction reaction (ORR) was studied on polycrystalline gold, Au(poly), modified by nanosized palladium islands in 0.1 M HClO4 solution using rotating disc electrode technique. Paladium was spontaneously deposited from 1 mM PdSO4 center dot 2H(2)O + 0.5 M H2SO4 solution for various deposition times at a submonolayer coverage. Topography of obtained Pd/Au(poly) surfaces was observed by tapping mode atomic force microscopy (AFM), while chemical surface composition changes were detected by simultaneously performed phase AFM. Deposited Pd islands were nonuniform in size and randomly distributed over the gold substrate. Size and number of Pd islands increase with the increase of the deposition time, and consequently surface coverage increases too. Deposited Pd was also identified by the changes in cyclic voltammetry (CV) profiles from which an active surface area was estimated. Obtained Pd/Au(poly) surfaces have shown a significant catalytic activity towards oxygen reduction reaction which increases with the increase of Pd islands coverage. The initial potential of ORR was shifted positively, while reaction pathway changes from 2e-reduction on pure gold to 4e-reduction on Pd modified gold. Additionally, obtained Pd/Au(poly) surfaces have shown a significant activity towards hydrogen peroxide reduction (HPRR), which appear as an intermediate during ORR. This supports the assumption that ORR on Pd/Au(poly) occurs partly through 4e-series reduction pathway, the fraction of which increases with the increase of Pd coverage.",
publisher = "Oxford : Pergamon-Elsevier Science Ltd",
journal = "Electrochimica Acta",
title = "Catalysis of oxygen reduction on Au modified by Pd nanoislands in perchloric acid solution",
volume = "64",
pages = "140-146",
doi = "10.1016/j.electacta.2011.12.130"
}

Srejić, I., Smiljanić, M., Grgur, B. N., Rakočević, Z. Lj.,& Štrbac, S.. (2012). Catalysis of oxygen reduction on Au modified by Pd nanoislands in perchloric acid solution. in Electrochimica Acta
Oxford : Pergamon-Elsevier Science Ltd., 64, 140-146.
https://doi.org/10.1016/j.electacta.2011.12.130

Srejić I, Smiljanić M, Grgur BN, Rakočević ZL, Štrbac S. Catalysis of oxygen reduction on Au modified by Pd nanoislands in perchloric acid solution. in Electrochimica Acta. 2012;64:140-146.
doi:10.1016/j.electacta.2011.12.130 .

Srejić, Irina, Smiljanić, Milutin, Grgur, Branimir N., Rakočević, Zlatko Lj., Štrbac, Svetlana, "Catalysis of oxygen reduction on Au modified by Pd nanoislands in perchloric acid solution" in Electrochimica Acta, 64 (2012):140-146,
https://doi.org/10.1016/j.electacta.2011.12.130 . .

TY  - JOUR
AU  - Jambrec, Daliborka
AU  - Gvozdenović, Milica M.
AU  - Antov, Mirjana
AU  - Grgur, Branimir N.
AU  - Jokić, Bojan
AU  - Stevanović, Jasmina
AU  - Jugović, Branimir
PY  - 2012
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/975
AB  - Electrochemical deposition of polyaniline (PANI) on graphite electrode was performed galvanostaticaly at constant current density in the range of 1.0 - 5.0 mA cm(-2) from aqueous acidic electrolyte containing aniline monomer. Based on ratio of doping/dedoping charge capacities, it was estimated that current density of 2.0 mA cm(-2) was optimal. The structure of the electrochemically synthesized PANI was fibrous, uniform and three dimensional with highly developed surface. Immobilization of glucose oxidise (GOx) was achieved by cross linking via glutaraldehyde and the efficiency of the immobilization was determined spectrophotometrically. Chronoamperometric curves were recorded at different glucose concentrations and used to estimate the apparent Michaelis constant, which was shown to be 0.27 mM. The storage stability of the PANI enzyme electrode was also estimated.
PB  - Inst Materials Physics, Bucharest
T2  - Digest Journal of Nanomaterials and Biostructures
T1  - Electrochemically deposited nano fibrous polyanilne for amperometric determination of glucose
VL  - 7
IS  - 2
SP  - 785
EP  - 794
UR  - https://hdl.handle.net/21.15107/rcub_dais_469
ER  - 

@article{
author = "Jambrec, Daliborka and Gvozdenović, Milica M. and Antov, Mirjana and Grgur, Branimir N. and Jokić, Bojan and Stevanović, Jasmina and Jugović, Branimir",
year = "2012",
abstract = "Electrochemical deposition of polyaniline (PANI) on graphite electrode was performed galvanostaticaly at constant current density in the range of 1.0 - 5.0 mA cm(-2) from aqueous acidic electrolyte containing aniline monomer. Based on ratio of doping/dedoping charge capacities, it was estimated that current density of 2.0 mA cm(-2) was optimal. The structure of the electrochemically synthesized PANI was fibrous, uniform and three dimensional with highly developed surface. Immobilization of glucose oxidise (GOx) was achieved by cross linking via glutaraldehyde and the efficiency of the immobilization was determined spectrophotometrically. Chronoamperometric curves were recorded at different glucose concentrations and used to estimate the apparent Michaelis constant, which was shown to be 0.27 mM. The storage stability of the PANI enzyme electrode was also estimated.",
publisher = "Inst Materials Physics, Bucharest",
journal = "Digest Journal of Nanomaterials and Biostructures",
title = "Electrochemically deposited nano fibrous polyanilne for amperometric determination of glucose",
volume = "7",
number = "2",
pages = "785-794",
url = "https://hdl.handle.net/21.15107/rcub_dais_469"
}

Jambrec, D., Gvozdenović, M. M., Antov, M., Grgur, B. N., Jokić, B., Stevanović, J.,& Jugović, B.. (2012). Electrochemically deposited nano fibrous polyanilne for amperometric determination of glucose. in Digest Journal of Nanomaterials and Biostructures
Inst Materials Physics, Bucharest., 7(2), 785-794.
https://hdl.handle.net/21.15107/rcub_dais_469

Jambrec D, Gvozdenović MM, Antov M, Grgur BN, Jokić B, Stevanović J, Jugović B. Electrochemically deposited nano fibrous polyanilne for amperometric determination of glucose. in Digest Journal of Nanomaterials and Biostructures. 2012;7(2):785-794.
https://hdl.handle.net/21.15107/rcub_dais_469 .

Jambrec, Daliborka, Gvozdenović, Milica M., Antov, Mirjana, Grgur, Branimir N., Jokić, Bojan, Stevanović, Jasmina, Jugović, Branimir, "Electrochemically deposited nano fibrous polyanilne for amperometric determination of glucose" in Digest Journal of Nanomaterials and Biostructures, 7, no. 2 (2012):785-794,
https://hdl.handle.net/21.15107/rcub_dais_469 .

TY  - JOUR
AU  - Smiljanić, Milutin
AU  - Srejić, Irina
AU  - Grgur, Branimir N.
AU  - Rakočević, Zlatko Lj.
AU  - Štrbac, Svetlana
PY  - 2012
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1059
AB  - Hydrogen evolution reaction was studied on Au(111) modified by palladium spontaneously deposited on the Au(111) surface from (1 mM PdSO4 center dot 2 H2O + 0.5 M H2SO4) solution at a submonolayer coverage. Number and size of Pd islands increased with the increase of the deposition time as observed by ex situ surface topography atomic force microscopy (AFM). The overall coverage of the underlying Au(111) surface by the deposited Pd islands was estimated from simultaneously acquired phase AFM images, which provided a clear contrast between different materials. The obtained Pd/Au(111) surfaces have shown a significant catalytic activity toward hydrogen evolution reaction in 0.5 M H2SO4 solution. This is discussed with respect to Pd islands size and coverage and to the influence of an electronic effect induced in Pd islands by the underlying Au(111) substrate.
PB  - Springer, New York
T2  - Electrocatalysis
T1  - Catalysis of Hydrogen Evolution on Au(111) Modified by Spontaneously Deposited Pd Nanoislands
VL  - 3
IS  - 3-4
SP  - 369
EP  - 375
DO  - 10.1007/s12678-012-0093-2
ER  - 

@article{
author = "Smiljanić, Milutin and Srejić, Irina and Grgur, Branimir N. and Rakočević, Zlatko Lj. and Štrbac, Svetlana",
year = "2012",
abstract = "Hydrogen evolution reaction was studied on Au(111) modified by palladium spontaneously deposited on the Au(111) surface from (1 mM PdSO4 center dot 2 H2O + 0.5 M H2SO4) solution at a submonolayer coverage. Number and size of Pd islands increased with the increase of the deposition time as observed by ex situ surface topography atomic force microscopy (AFM). The overall coverage of the underlying Au(111) surface by the deposited Pd islands was estimated from simultaneously acquired phase AFM images, which provided a clear contrast between different materials. The obtained Pd/Au(111) surfaces have shown a significant catalytic activity toward hydrogen evolution reaction in 0.5 M H2SO4 solution. This is discussed with respect to Pd islands size and coverage and to the influence of an electronic effect induced in Pd islands by the underlying Au(111) substrate.",
publisher = "Springer, New York",
journal = "Electrocatalysis",
title = "Catalysis of Hydrogen Evolution on Au(111) Modified by Spontaneously Deposited Pd Nanoislands",
volume = "3",
number = "3-4",
pages = "369-375",
doi = "10.1007/s12678-012-0093-2"
}

Smiljanić, M., Srejić, I., Grgur, B. N., Rakočević, Z. Lj.,& Štrbac, S.. (2012). Catalysis of Hydrogen Evolution on Au(111) Modified by Spontaneously Deposited Pd Nanoislands. in Electrocatalysis
Springer, New York., 3(3-4), 369-375.
https://doi.org/10.1007/s12678-012-0093-2

Smiljanić M, Srejić I, Grgur BN, Rakočević ZL, Štrbac S. Catalysis of Hydrogen Evolution on Au(111) Modified by Spontaneously Deposited Pd Nanoislands. in Electrocatalysis. 2012;3(3-4):369-375.
doi:10.1007/s12678-012-0093-2 .

Smiljanić, Milutin, Srejić, Irina, Grgur, Branimir N., Rakočević, Zlatko Lj., Štrbac, Svetlana, "Catalysis of Hydrogen Evolution on Au(111) Modified by Spontaneously Deposited Pd Nanoislands" in Electrocatalysis, 3, no. 3-4 (2012):369-375,
https://doi.org/10.1007/s12678-012-0093-2 . .

TY  - JOUR
AU  - Gvozdenović, Milica M.
AU  - Jugović, Branimir
AU  - Jambrec, Daliborka
AU  - Stevanović, Jasmina
AU  - Grgur, Branimir N.
PY  - 2012
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1081
AB  - Polyaniline is probably the most investigated electroconducting polymer. This popularity is a result of its important features: existence of various oxidation states, electrical and optical activity, low cost monomer, red/ox reversibility, environmental stability, ease of both chemical and electrochemical synthesis etc. These unique features are partly inherited from its polymeric origin and partly aroused from its conductivity and could be considered for practical application in: electrochemical systems for energy storage and conversion, electronic devices, electromagnetic and microwave shielding materials, sensors, biosensors and corrosion protection as well. The motivation of application of polyaniline in corrosion protection of metals and alloys is replacement of environmentally hazardous materials, e.g. chromates in coating systems. Up to day, lot of studies on various metals both on iron, steels and non-ferrous metals and alloys were performed. The studies involve investigation on individual polyaniline coatings and polyaniline in coating systems. Owing to variation in experimental procedure (substrate, substrate preparation, coating type, corrosion environment, test method etc..) it is unlikely to propose unique mechanism for corrosion protection of metals in the presence of polyaniline. However, most of the literature is interpreted in terms of general mechanisms of corrosion protection, barrier and anodic protection.
AB  - Polianilin je najproučavaniji elektroprovodni polimer. Ova popularnost polianilina je posledica jedinstvenih svojstava, delom nasleđenih od polimerne prirode, a delom ostvarenih provodljivošću. Najvažnija svojstva polianilina: postojanje više oksidacionih stanja, elektronska provodljivost, optička aktivnost, postojanost u spoljašnjoj sredini, mogućnost hemijske i elektrohemisjke sinteze i niska cena monomera nalaze primenu u mnogim oblstima: elektrohemisjkim sistemima za skladištenje i proizvodnju električne energije, elektronici, za izradu sensorskhih i biosenzorskih elektroda, za izradu antistatičkih i materijala mikrotalasnih i magnetnih štitova i u zaštiti metala i legura od korozije. Primena polianilina u zaštiti od korozije je prvenstveno motivisana potrebom zamene toksičnih materijala iz sistema prevlaka. Postoji dosta literaturnih podataka iz ove oblasti. Ipak, imajući u vidu raznovrsnost metala i legura, korozionih sredina, postupaka pripreme materijala, nanošenja prevlaka i vrsta prevlaka, kao i eksperimentalnih procedura i observacija, praktično je nemoguće uspostaviti jedinstven mehanizam antikorozione zaštite metala u prisustvu polianilina. Najcitiraniji i najpopularniji mehanizmi koji se mogu naći u literaturi obuhvataju barijerni mehanizam i mehanizam anodne zaštite.
PB  - Belgrade, Serbia : Engineering Society for Corrosion
T2  - Zaštita materijala
T1  - Application of polyaniline in corrosion protection of metals
T1  - Primena polianilina u zaštiti metala od korozije
VL  - 53
IS  - 4
SP  - 353
EP  - 360
UR  - https://hdl.handle.net/21.15107/rcub_cer_1081
ER  - 

@article{
author = "Gvozdenović, Milica M. and Jugović, Branimir and Jambrec, Daliborka and Stevanović, Jasmina and Grgur, Branimir N.",
year = "2012",
abstract = "Polyaniline is probably the most investigated electroconducting polymer. This popularity is a result of its important features: existence of various oxidation states, electrical and optical activity, low cost monomer, red/ox reversibility, environmental stability, ease of both chemical and electrochemical synthesis etc. These unique features are partly inherited from its polymeric origin and partly aroused from its conductivity and could be considered for practical application in: electrochemical systems for energy storage and conversion, electronic devices, electromagnetic and microwave shielding materials, sensors, biosensors and corrosion protection as well. The motivation of application of polyaniline in corrosion protection of metals and alloys is replacement of environmentally hazardous materials, e.g. chromates in coating systems. Up to day, lot of studies on various metals both on iron, steels and non-ferrous metals and alloys were performed. The studies involve investigation on individual polyaniline coatings and polyaniline in coating systems. Owing to variation in experimental procedure (substrate, substrate preparation, coating type, corrosion environment, test method etc..) it is unlikely to propose unique mechanism for corrosion protection of metals in the presence of polyaniline. However, most of the literature is interpreted in terms of general mechanisms of corrosion protection, barrier and anodic protection., Polianilin je najproučavaniji elektroprovodni polimer. Ova popularnost polianilina je posledica jedinstvenih svojstava, delom nasleđenih od polimerne prirode, a delom ostvarenih provodljivošću. Najvažnija svojstva polianilina: postojanje više oksidacionih stanja, elektronska provodljivost, optička aktivnost, postojanost u spoljašnjoj sredini, mogućnost hemijske i elektrohemisjke sinteze i niska cena monomera nalaze primenu u mnogim oblstima: elektrohemisjkim sistemima za skladištenje i proizvodnju električne energije, elektronici, za izradu sensorskhih i biosenzorskih elektroda, za izradu antistatičkih i materijala mikrotalasnih i magnetnih štitova i u zaštiti metala i legura od korozije. Primena polianilina u zaštiti od korozije je prvenstveno motivisana potrebom zamene toksičnih materijala iz sistema prevlaka. Postoji dosta literaturnih podataka iz ove oblasti. Ipak, imajući u vidu raznovrsnost metala i legura, korozionih sredina, postupaka pripreme materijala, nanošenja prevlaka i vrsta prevlaka, kao i eksperimentalnih procedura i observacija, praktično je nemoguće uspostaviti jedinstven mehanizam antikorozione zaštite metala u prisustvu polianilina. Najcitiraniji i najpopularniji mehanizmi koji se mogu naći u literaturi obuhvataju barijerni mehanizam i mehanizam anodne zaštite.",
publisher = "Belgrade, Serbia : Engineering Society for Corrosion",
journal = "Zaštita materijala",
title = "Application of polyaniline in corrosion protection of metals, Primena polianilina u zaštiti metala od korozije",
volume = "53",
number = "4",
pages = "353-360",
url = "https://hdl.handle.net/21.15107/rcub_cer_1081"
}

Gvozdenović, M. M., Jugović, B., Jambrec, D., Stevanović, J.,& Grgur, B. N.. (2012). Application of polyaniline in corrosion protection of metals. in Zaštita materijala
Belgrade, Serbia : Engineering Society for Corrosion., 53(4), 353-360.
https://hdl.handle.net/21.15107/rcub_cer_1081

Gvozdenović MM, Jugović B, Jambrec D, Stevanović J, Grgur BN. Application of polyaniline in corrosion protection of metals. in Zaštita materijala. 2012;53(4):353-360.
https://hdl.handle.net/21.15107/rcub_cer_1081 .

Gvozdenović, Milica M., Jugović, Branimir, Jambrec, Daliborka, Stevanović, Jasmina, Grgur, Branimir N., "Application of polyaniline in corrosion protection of metals" in Zaštita materijala, 53, no. 4 (2012):353-360,
https://hdl.handle.net/21.15107/rcub_cer_1081 .

TY  - CONF
AU  - Gvozdenović, Milica M.
AU  - Jugović, Branimir
AU  - Jambrec, Daliborka
AU  - Grgur, Branimir N.
AU  - Trišović, Tomislav
AU  - Stevanović, Jasmina
PY  - 2012
UR  - http://dais.sanu.ac.rs/123456789/492
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2597
AB  - Polyaniline (PANI) was electrochemically synthesized on graphite electrode galvanostaticaly from aqueous solution of 0.25 mol dm-3 aniline and 0.5 mol dm-3 p-toluenesulfonic acid. Charge capacity available for the exchange and the total theoretical weight of polyaniline polymerized on graphite electrode was determined. Characterization polianiline electrode was performed by cyclic voltametry in 0.5 mol dm-3 HCl. Based on the PANI electrodes behavior during the cyclization, was tested the possibility of practical application of polyaniline doped p-toluenesulfonic acid as the anode material of secondary electrochemical power sources.
PB  - Tatranské Matliare : Slovak Society of Chemical Engineering
C3  - Proceedings of the 39th International Conference of Slovak Society of Chemical Engineering
T1  - The influence of current density on charge/discharge characteristics of polyaniline electrode
SP  - 1467
EP  - 1471
UR  - https://hdl.handle.net/21.15107/rcub_dais_492
ER  - 

@conference{
author = "Gvozdenović, Milica M. and Jugović, Branimir and Jambrec, Daliborka and Grgur, Branimir N. and Trišović, Tomislav and Stevanović, Jasmina",
year = "2012",
abstract = "Polyaniline (PANI) was electrochemically synthesized on graphite electrode galvanostaticaly from aqueous solution of 0.25 mol dm-3 aniline and 0.5 mol dm-3 p-toluenesulfonic acid. Charge capacity available for the exchange and the total theoretical weight of polyaniline polymerized on graphite electrode was determined. Characterization polianiline electrode was performed by cyclic voltametry in 0.5 mol dm-3 HCl. Based on the PANI electrodes behavior during the cyclization, was tested the possibility of practical application of polyaniline doped p-toluenesulfonic acid as the anode material of secondary electrochemical power sources.",
publisher = "Tatranské Matliare : Slovak Society of Chemical Engineering",
journal = "Proceedings of the 39th International Conference of Slovak Society of Chemical Engineering",
title = "The influence of current density on charge/discharge characteristics of polyaniline electrode",
pages = "1467-1471",
url = "https://hdl.handle.net/21.15107/rcub_dais_492"
}

Gvozdenović, M. M., Jugović, B., Jambrec, D., Grgur, B. N., Trišović, T.,& Stevanović, J.. (2012). The influence of current density on charge/discharge characteristics of polyaniline electrode. in Proceedings of the 39th International Conference of Slovak Society of Chemical Engineering
Tatranské Matliare : Slovak Society of Chemical Engineering., 1467-1471.
https://hdl.handle.net/21.15107/rcub_dais_492

Gvozdenović MM, Jugović B, Jambrec D, Grgur BN, Trišović T, Stevanović J. The influence of current density on charge/discharge characteristics of polyaniline electrode. in Proceedings of the 39th International Conference of Slovak Society of Chemical Engineering. 2012;:1467-1471.
https://hdl.handle.net/21.15107/rcub_dais_492 .

Gvozdenović, Milica M., Jugović, Branimir, Jambrec, Daliborka, Grgur, Branimir N., Trišović, Tomislav, Stevanović, Jasmina, "The influence of current density on charge/discharge characteristics of polyaniline electrode" in Proceedings of the 39th International Conference of Slovak Society of Chemical Engineering (2012):1467-1471,
https://hdl.handle.net/21.15107/rcub_dais_492 .

TY  - JOUR
AU  - Gvozdenović, Milica M.
AU  - Jugović, Branimir
AU  - Trišović, Tomislav
AU  - Stevanović, Jasmina
AU  - Plazinić, Milan
AU  - Grgur, Branimir N.
PY  - 2012
UR  - http://dais.sanu.ac.rs/123456789/468
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2847
AB  - Polyaniline (PANI) anode, electrochemically formed on graphite from aniline containing sulfuric acid solution, and electrochemically formed thin film lead dioxide cathode, were investigated for possible applications as electrode materials in PANI/H2SO4/PbO2 aqueous based rechargeable power sources. The stimulation of charge/discharge characteristics of the cell, based on half cell reactions investigations, was evaluated. Charging of the cell would occur in the voltage range of 1.20 and 1.70 V, while discharge is expected in the voltage range of 1.35 and 1.00 V.
PB  - Hunedoara : University Politehnica Timisoara,  Faculty of Engineering Hunedoara
T2  - Annals of the Faculty of Engineering Hunedoara: International Journal of Engineering
T1  - Electrochemical characteristics of polyaniline/lead-dioxide power source
VL  - 10
IS  - 3
SP  - 445
EP  - 448
UR  - https://hdl.handle.net/21.15107/rcub_dais_468
ER  - 

@article{
author = "Gvozdenović, Milica M. and Jugović, Branimir and Trišović, Tomislav and Stevanović, Jasmina and Plazinić, Milan and Grgur, Branimir N.",
year = "2012",
abstract = "Polyaniline (PANI) anode, electrochemically formed on graphite from aniline containing sulfuric acid solution, and electrochemically formed thin film lead dioxide cathode, were investigated for possible applications as electrode materials in PANI/H2SO4/PbO2 aqueous based rechargeable power sources. The stimulation of charge/discharge characteristics of the cell, based on half cell reactions investigations, was evaluated. Charging of the cell would occur in the voltage range of 1.20 and 1.70 V, while discharge is expected in the voltage range of 1.35 and 1.00 V.",
publisher = "Hunedoara : University Politehnica Timisoara,  Faculty of Engineering Hunedoara",
journal = "Annals of the Faculty of Engineering Hunedoara: International Journal of Engineering",
title = "Electrochemical characteristics of polyaniline/lead-dioxide power source",
volume = "10",
number = "3",
pages = "445-448",
url = "https://hdl.handle.net/21.15107/rcub_dais_468"
}

Gvozdenović, M. M., Jugović, B., Trišović, T., Stevanović, J., Plazinić, M.,& Grgur, B. N.. (2012). Electrochemical characteristics of polyaniline/lead-dioxide power source. in Annals of the Faculty of Engineering Hunedoara: International Journal of Engineering
Hunedoara : University Politehnica Timisoara,  Faculty of Engineering Hunedoara., 10(3), 445-448.
https://hdl.handle.net/21.15107/rcub_dais_468

Gvozdenović MM, Jugović B, Trišović T, Stevanović J, Plazinić M, Grgur BN. Electrochemical characteristics of polyaniline/lead-dioxide power source. in Annals of the Faculty of Engineering Hunedoara: International Journal of Engineering. 2012;10(3):445-448.
https://hdl.handle.net/21.15107/rcub_dais_468 .

Gvozdenović, Milica M., Jugović, Branimir, Trišović, Tomislav, Stevanović, Jasmina, Plazinić, Milan, Grgur, Branimir N., "Electrochemical characteristics of polyaniline/lead-dioxide power source" in Annals of the Faculty of Engineering Hunedoara: International Journal of Engineering, 10, no. 3 (2012):445-448,
https://hdl.handle.net/21.15107/rcub_dais_468 .

TY  - CONF
AU  - Gvozdenović, Milica M.
AU  - Jugović, Branimir
AU  - Jambrec, Daliborka
AU  - Grgur, Branimir N.
AU  - Trišović, Tomislav
AU  - Stevanović, Jasmina
PY  - 2012
UR  - http://dais.sanu.ac.rs/123456789/141
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/3150
AB  - Poster presented at the 39th International Conference of Slovak Society of Chemical Engineering, Tatranske Matliare, Slovakia, May 21–25, 2012
T1  - The influence of current density on charge/discharge characteristics of polyaniline electrode
UR  - https://hdl.handle.net/21.15107/rcub_dais_492
ER  - 

@conference{
author = "Gvozdenović, Milica M. and Jugović, Branimir and Jambrec, Daliborka and Grgur, Branimir N. and Trišović, Tomislav and Stevanović, Jasmina",
year = "2012",
abstract = "Poster presented at the 39th International Conference of Slovak Society of Chemical Engineering, Tatranske Matliare, Slovakia, May 21–25, 2012",
title = "The influence of current density on charge/discharge characteristics of polyaniline electrode",
url = "https://hdl.handle.net/21.15107/rcub_dais_492"
}

Gvozdenović, M. M., Jugović, B., Jambrec, D., Grgur, B. N., Trišović, T.,& Stevanović, J.. (2012). The influence of current density on charge/discharge characteristics of polyaniline electrode. .
https://hdl.handle.net/21.15107/rcub_dais_492

Gvozdenović MM, Jugović B, Jambrec D, Grgur BN, Trišović T, Stevanović J. The influence of current density on charge/discharge characteristics of polyaniline electrode. 2012;.
https://hdl.handle.net/21.15107/rcub_dais_492 .

Gvozdenović, Milica M., Jugović, Branimir, Jambrec, Daliborka, Grgur, Branimir N., Trišović, Tomislav, Stevanović, Jasmina, "The influence of current density on charge/discharge characteristics of polyaniline electrode" (2012),
https://hdl.handle.net/21.15107/rcub_dais_492 .

TY  - CONF
AU  - Trišović, Tomislav
AU  - Jugović, Branimir
AU  - Gvozdenović, Milica M.
AU  - Stevanović, Jasmina
AU  - Grgur, Branimir N.
PY  - 2011
UR  - http://dais.sanu.ac.rs/123456789/546
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/3149
AB  - Paper published in 43rd International October Conference on Mining and Metallurgy - IOC 2011, October 12-15, 2011, Kladovo, Serbia: Proceedings, Bor : Technical Faculty, 2011.
PB  - Bor : Technical Faculty
C3  - 43rd International October Conference on Mining and Metallurgy - IOC 2011, October 12-15, 2011, Kladovo, Serbia: Proceedings
T1  - Electrochemical Water Treatment Devices
SP  - 259
EP  - 262
UR  - https://hdl.handle.net/21.15107/rcub_dais_546
ER  - 

@conference{
author = "Trišović, Tomislav and Jugović, Branimir and Gvozdenović, Milica M. and Stevanović, Jasmina and Grgur, Branimir N.",
year = "2011",
abstract = "Paper published in 43rd International October Conference on Mining and Metallurgy - IOC 2011, October 12-15, 2011, Kladovo, Serbia: Proceedings, Bor : Technical Faculty, 2011.",
publisher = "Bor : Technical Faculty",
journal = "43rd International October Conference on Mining and Metallurgy - IOC 2011, October 12-15, 2011, Kladovo, Serbia: Proceedings",
title = "Electrochemical Water Treatment Devices",
pages = "259-262",
url = "https://hdl.handle.net/21.15107/rcub_dais_546"
}

Trišović, T., Jugović, B., Gvozdenović, M. M., Stevanović, J.,& Grgur, B. N.. (2011). Electrochemical Water Treatment Devices. in 43rd International October Conference on Mining and Metallurgy - IOC 2011, October 12-15, 2011, Kladovo, Serbia: Proceedings
Bor : Technical Faculty., 259-262.
https://hdl.handle.net/21.15107/rcub_dais_546

Trišović T, Jugović B, Gvozdenović MM, Stevanović J, Grgur BN. Electrochemical Water Treatment Devices. in 43rd International October Conference on Mining and Metallurgy - IOC 2011, October 12-15, 2011, Kladovo, Serbia: Proceedings. 2011;:259-262.
https://hdl.handle.net/21.15107/rcub_dais_546 .

Trišović, Tomislav, Jugović, Branimir, Gvozdenović, Milica M., Stevanović, Jasmina, Grgur, Branimir N., "Electrochemical Water Treatment Devices" in 43rd International October Conference on Mining and Metallurgy - IOC 2011, October 12-15, 2011, Kladovo, Serbia: Proceedings (2011):259-262,
https://hdl.handle.net/21.15107/rcub_dais_546 .

TY  - JOUR
AU  - Gvozdenović, Milica M.
AU  - Jugović, Branimir
AU  - Stevanović, Jasmina
AU  - Grgur, Branimir N.
AU  - Trišović, Tomislav
AU  - Jugovic, Zvonimir S.
PY  - 2011
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/806
AB  - Electrochemical polymerization of polyaniline (PANI) coating on copper electrode was performed galvanostatically in the current density range between 0.50 and 1.25 mA cm(-2), from aqueous solution of 0.3 mol dm(-3) sodium benzoate and 0.2 mol dm(-3) aniline. The corrosion behavior of PANI coated copper and copper electrode exposed to 0.5 mol dm(-3) sodium chloride solution was investigated by potentiodynamic and electrochemical impedance spectroscopy techniques. It was observed that thin PANI (5 mu m) coating had provided efficient protection (similar to 96%) to copper in 0.5 mol dm(-3) sodium chloride solution. Unusual initial impedance behavior to that normally observed with conventional organic coatings was attributed to dedoping of benzoate anions from the polymer coating.
PB  - Elsevier Science Sa, Lausanne
T2  - Synthetic Metals
T1  - Electrochemical synthesis and corrosion behavior of polyaniline-benzoate coating on copper
VL  - 161
IS  - 13-14
SP  - 1313
EP  - 1318
DO  - 10.1016/j.synthmet.2011.04.029
ER  - 

@article{
author = "Gvozdenović, Milica M. and Jugović, Branimir and Stevanović, Jasmina and Grgur, Branimir N. and Trišović, Tomislav and Jugovic, Zvonimir S.",
year = "2011",
abstract = "Electrochemical polymerization of polyaniline (PANI) coating on copper electrode was performed galvanostatically in the current density range between 0.50 and 1.25 mA cm(-2), from aqueous solution of 0.3 mol dm(-3) sodium benzoate and 0.2 mol dm(-3) aniline. The corrosion behavior of PANI coated copper and copper electrode exposed to 0.5 mol dm(-3) sodium chloride solution was investigated by potentiodynamic and electrochemical impedance spectroscopy techniques. It was observed that thin PANI (5 mu m) coating had provided efficient protection (similar to 96%) to copper in 0.5 mol dm(-3) sodium chloride solution. Unusual initial impedance behavior to that normally observed with conventional organic coatings was attributed to dedoping of benzoate anions from the polymer coating.",
publisher = "Elsevier Science Sa, Lausanne",
journal = "Synthetic Metals",
title = "Electrochemical synthesis and corrosion behavior of polyaniline-benzoate coating on copper",
volume = "161",
number = "13-14",
pages = "1313-1318",
doi = "10.1016/j.synthmet.2011.04.029"
}

Gvozdenović, M. M., Jugović, B., Stevanović, J., Grgur, B. N., Trišović, T.,& Jugovic, Z. S.. (2011). Electrochemical synthesis and corrosion behavior of polyaniline-benzoate coating on copper. in Synthetic Metals
Elsevier Science Sa, Lausanne., 161(13-14), 1313-1318.
https://doi.org/10.1016/j.synthmet.2011.04.029

Gvozdenović MM, Jugović B, Stevanović J, Grgur BN, Trišović T, Jugovic ZS. Electrochemical synthesis and corrosion behavior of polyaniline-benzoate coating on copper. in Synthetic Metals. 2011;161(13-14):1313-1318.
doi:10.1016/j.synthmet.2011.04.029 .

Gvozdenović, Milica M., Jugović, Branimir, Stevanović, Jasmina, Grgur, Branimir N., Trišović, Tomislav, Jugovic, Zvonimir S., "Electrochemical synthesis and corrosion behavior of polyaniline-benzoate coating on copper" in Synthetic Metals, 161, no. 13-14 (2011):1313-1318,
https://doi.org/10.1016/j.synthmet.2011.04.029 . .

TY  - JOUR
AU  - Elkais, Ali Ramadan
AU  - Gvozdenović, Milica M.
AU  - Jugović, Branimir
AU  - Stevanović, Jasmina
AU  - Nikolić, Nebojša D.
AU  - Grgur, Branimir N.
PY  - 2011
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/917
AB  - The polyaniline thin film electrode and powder have been synthesized on graphite electrodes from 0.5 M hydrochloric acid solution under galvanostatic conditions. The water insoluble and acetone soluble polyaniline mass fractions of the powder, as well as the polymerization efficiency, based on the emeraldine salt have been determined. The morphology of the obtained emeraldine salt powder has been investigated by the optical microscopy.
PB  - Elsevier Science Sa, Lausanne
T2  - Progress in Organic Coatings
T1  - Electrochemical synthesis and characterization of polyaniline thin film and polyaniline powder
VL  - 71
IS  - 1
SP  - 32
EP  - 35
DO  - 10.1016/j.porgcoat.2010.12.004
ER  - 

@article{
author = "Elkais, Ali Ramadan and Gvozdenović, Milica M. and Jugović, Branimir and Stevanović, Jasmina and Nikolić, Nebojša D. and Grgur, Branimir N.",
year = "2011",
abstract = "The polyaniline thin film electrode and powder have been synthesized on graphite electrodes from 0.5 M hydrochloric acid solution under galvanostatic conditions. The water insoluble and acetone soluble polyaniline mass fractions of the powder, as well as the polymerization efficiency, based on the emeraldine salt have been determined. The morphology of the obtained emeraldine salt powder has been investigated by the optical microscopy.",
publisher = "Elsevier Science Sa, Lausanne",
journal = "Progress in Organic Coatings",
title = "Electrochemical synthesis and characterization of polyaniline thin film and polyaniline powder",
volume = "71",
number = "1",
pages = "32-35",
doi = "10.1016/j.porgcoat.2010.12.004"
}

Elkais, A. R., Gvozdenović, M. M., Jugović, B., Stevanović, J., Nikolić, N. D.,& Grgur, B. N.. (2011). Electrochemical synthesis and characterization of polyaniline thin film and polyaniline powder. in Progress in Organic Coatings
Elsevier Science Sa, Lausanne., 71(1), 32-35.
https://doi.org/10.1016/j.porgcoat.2010.12.004

Elkais AR, Gvozdenović MM, Jugović B, Stevanović J, Nikolić ND, Grgur BN. Electrochemical synthesis and characterization of polyaniline thin film and polyaniline powder. in Progress in Organic Coatings. 2011;71(1):32-35.
doi:10.1016/j.porgcoat.2010.12.004 .

Elkais, Ali Ramadan, Gvozdenović, Milica M., Jugović, Branimir, Stevanović, Jasmina, Nikolić, Nebojša D., Grgur, Branimir N., "Electrochemical synthesis and characterization of polyaniline thin film and polyaniline powder" in Progress in Organic Coatings, 71, no. 1 (2011):32-35,
https://doi.org/10.1016/j.porgcoat.2010.12.004 . .

TY  - JOUR
AU  - Gvozdenović, Milica M.
AU  - Jugović, Branimir
AU  - Trišović, Tomislav
AU  - Stevanović, Jasmina
AU  - Grgur, Branimir N.
PY  - 2011
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/939
AB  - Polyaniline electrode (PANI) was formed electrochemically at graphite electrode. Electrochemical polymerization was performed at constant current density of 2.0 mA cm-2 from aqueous solution of 1.0 mol dm -3 HCl with addition of 0.25 mol dm-3 aniline monomer. Electrochemical characterization of the PANI electrode in chloride and chloride/citrate electrolyte was performed using cyclic voltammetry and galvanostatic measurement in order to study the influence of citrate ions on charge/discharge capability and cycling efficiency. It was observed that, for anodic potential 0.32 V, higher electrode capacity of PANI electrode in chloride/citrate electrolyte was obtained, comparing to chloride electrolyte, indicating positive effect of citrate ions on cycling characteristics. On the other hand, for higher anodic potential limit of 0.50 V, faster decrease of the electrode capacity in chloride/citrate electrolyte was observed. It was suggested that influence of both chloride and citrate anions had exhibited influence on electrochemical behavior of PANI electrode in citrate containing electrolyte.
T2  - Materials Chemistry and Physics
T1  - Electrochemical characterization of polyaniline electrode in ammonium citrate containing electrolyte
VL  - 125
IS  - 3
SP  - 601
EP  - 605
DO  - 10.1016/j.matchemphys.2010.10.011
ER  - 

@article{
author = "Gvozdenović, Milica M. and Jugović, Branimir and Trišović, Tomislav and Stevanović, Jasmina and Grgur, Branimir N.",
year = "2011",
abstract = "Polyaniline electrode (PANI) was formed electrochemically at graphite electrode. Electrochemical polymerization was performed at constant current density of 2.0 mA cm-2 from aqueous solution of 1.0 mol dm -3 HCl with addition of 0.25 mol dm-3 aniline monomer. Electrochemical characterization of the PANI electrode in chloride and chloride/citrate electrolyte was performed using cyclic voltammetry and galvanostatic measurement in order to study the influence of citrate ions on charge/discharge capability and cycling efficiency. It was observed that, for anodic potential 0.32 V, higher electrode capacity of PANI electrode in chloride/citrate electrolyte was obtained, comparing to chloride electrolyte, indicating positive effect of citrate ions on cycling characteristics. On the other hand, for higher anodic potential limit of 0.50 V, faster decrease of the electrode capacity in chloride/citrate electrolyte was observed. It was suggested that influence of both chloride and citrate anions had exhibited influence on electrochemical behavior of PANI electrode in citrate containing electrolyte.",
journal = "Materials Chemistry and Physics",
title = "Electrochemical characterization of polyaniline electrode in ammonium citrate containing electrolyte",
volume = "125",
number = "3",
pages = "601-605",
doi = "10.1016/j.matchemphys.2010.10.011"
}

Gvozdenović, M. M., Jugović, B., Trišović, T., Stevanović, J.,& Grgur, B. N.. (2011). Electrochemical characterization of polyaniline electrode in ammonium citrate containing electrolyte. in Materials Chemistry and Physics, 125(3), 601-605.
https://doi.org/10.1016/j.matchemphys.2010.10.011

Gvozdenović MM, Jugović B, Trišović T, Stevanović J, Grgur BN. Electrochemical characterization of polyaniline electrode in ammonium citrate containing electrolyte. in Materials Chemistry and Physics. 2011;125(3):601-605.
doi:10.1016/j.matchemphys.2010.10.011 .

Gvozdenović, Milica M., Jugović, Branimir, Trišović, Tomislav, Stevanović, Jasmina, Grgur, Branimir N., "Electrochemical characterization of polyaniline electrode in ammonium citrate containing electrolyte" in Materials Chemistry and Physics, 125, no. 3 (2011):601-605,
https://doi.org/10.1016/j.matchemphys.2010.10.011 . .

TY  - CONF
AU  - Jugović, Branimir
AU  - Gvozdenović, Milica M.
AU  - Trišović, Tomislav
AU  - Stevanović, Jasmina
AU  - Grgur, Branimir N.
PY  - 2011
UR  - http://dais.sanu.ac.rs/123456789/548
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2616
AB  - Polyaniline electrode, was obtained by electrochemical polymerization at constant current density of 2.0 mA cm-2 from aqueous solution of 1.0 mol dm-3 HCl containing 0.25 mol dm-3 aniline. Electrochemical characterization of the polyaniline electrode in chloride and chloride/citrate electrolyte, for different anodic potential limits, was performed using cyclic voltammetry and galvanostatic measurements. It was observed that for anodic potential 0.32 V, higher electrode capacity in chloride/citrate was obtained. For anodic potential limit of 0.50 V, faster decrease of theelectrode capacity in chloride/citrate electrolyte was also observed. It was suggested that influence of both chloride and citrate anions has to be taken into account.
PB  - Tatranské Matliare : Slovak Society of Chemical Engineering
C3  - Proceedings of the 38th International Conference of Slovak Society of Chemical Engineering
T1  - Electrochemical behavior of polyaniline in chloride/citrate electrolyte
SP  - 963
EP  - 967
UR  - https://hdl.handle.net/21.15107/rcub_dais_548
ER  - 

@conference{
author = "Jugović, Branimir and Gvozdenović, Milica M. and Trišović, Tomislav and Stevanović, Jasmina and Grgur, Branimir N.",
year = "2011",
abstract = "Polyaniline electrode, was obtained by electrochemical polymerization at constant current density of 2.0 mA cm-2 from aqueous solution of 1.0 mol dm-3 HCl containing 0.25 mol dm-3 aniline. Electrochemical characterization of the polyaniline electrode in chloride and chloride/citrate electrolyte, for different anodic potential limits, was performed using cyclic voltammetry and galvanostatic measurements. It was observed that for anodic potential 0.32 V, higher electrode capacity in chloride/citrate was obtained. For anodic potential limit of 0.50 V, faster decrease of theelectrode capacity in chloride/citrate electrolyte was also observed. It was suggested that influence of both chloride and citrate anions has to be taken into account.",
publisher = "Tatranské Matliare : Slovak Society of Chemical Engineering",
journal = "Proceedings of the 38th International Conference of Slovak Society of Chemical Engineering",
title = "Electrochemical behavior of polyaniline in chloride/citrate electrolyte",
pages = "963-967",
url = "https://hdl.handle.net/21.15107/rcub_dais_548"
}

Jugović, B., Gvozdenović, M. M., Trišović, T., Stevanović, J.,& Grgur, B. N.. (2011). Electrochemical behavior of polyaniline in chloride/citrate electrolyte. in Proceedings of the 38th International Conference of Slovak Society of Chemical Engineering
Tatranské Matliare : Slovak Society of Chemical Engineering., 963-967.
https://hdl.handle.net/21.15107/rcub_dais_548

Jugović B, Gvozdenović MM, Trišović T, Stevanović J, Grgur BN. Electrochemical behavior of polyaniline in chloride/citrate electrolyte. in Proceedings of the 38th International Conference of Slovak Society of Chemical Engineering. 2011;:963-967.
https://hdl.handle.net/21.15107/rcub_dais_548 .

Jugović, Branimir, Gvozdenović, Milica M., Trišović, Tomislav, Stevanović, Jasmina, Grgur, Branimir N., "Electrochemical behavior of polyaniline in chloride/citrate electrolyte" in Proceedings of the 38th International Conference of Slovak Society of Chemical Engineering (2011):963-967,
https://hdl.handle.net/21.15107/rcub_dais_548 .