Stanković, Slavka

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  • Stanković, Slavka (2)
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Noble metal binding on macroporous poly(GMA-co-EGDMA) modified with ethylenediamine

Nastasović, Aleksandra; Jovanović, Slobodan M.; Jakovljević, Dragica; Stanković, Slavka; Onjia, Antonije E.

(Serbian Chemical Society, 2004)

TY  - JOUR
AU  - Nastasović, Aleksandra
AU  - Jovanović, Slobodan M.
AU  - Jakovljević, Dragica
AU  - Stanković, Slavka
AU  - Onjia, Antonije E.
PY  - 2004
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/163
AB  - Macroporous crosslinked poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate), p(GME), was synthesized by suspension copolymerization and modified by reaction of the pendant epoxy groups with ethylenediamine. The sorption rate and capacity of themodified copolymer, p(GME)-en for Rh(III) Au(III) and Pt(IV) ions were determined in batch experiments under non-competitive conditions. The uptake of Rh(III) was faster than those ofAu(III) and Pt(IV). The sorption capacity for Pt(IV)was determined in the pHrange 0.9–6.0. The maximum Pt(IV) uptake capacity onto p(GME)-en at pH 5.5 was 1.30 mmol/g.
AB  - Umreženi makroporozni poli(glicidilmetakrilat-ko-etilenglikoldimetakrilat) sintetizovan je suspenzionom kopolimerizacijom i modifikovan reakcijom bočnih epoksidnih grupa sa etilendiaminom. Brzina sorpcije i kapacitet modifikovanog kopolimera, poli(GME)-en, za sorpciju Rh(III), Au(III) i Pt(IV) jona određeni su šaržnim eksperimentima pri nekompetitivnim uslovima. Utvrđeno je da je sorpcija Rh(III) jona na poli(GME)-en brža od sorpcije Au(III) i Pt(IV) jona. Kapacitet sorpcije Pt(IV) jona određen je u opsegu pH 0,9 – 6,0. Maksimalna količina Pt(IV) jona vezanih za p(GME)-en pri pH 5,5 iznosi 1,30 mmol/g.
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Noble metal binding on macroporous poly(GMA-co-EGDMA) modified with ethylenediamine
T1  - Vezivanje plemenitih metala za makroporozni poli(GMA-co-EGDMA)kopolimer modifikovan sa etilendiaminom
VL  - 69
IS  - 6
SP  - 455
EP  - 460
DO  - 10.2298/JSC0406455N
ER  - 
@article{
author = "Nastasović, Aleksandra and Jovanović, Slobodan M. and Jakovljević, Dragica and Stanković, Slavka and Onjia, Antonije E.",
year = "2004",
abstract = "Macroporous crosslinked poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate), p(GME), was synthesized by suspension copolymerization and modified by reaction of the pendant epoxy groups with ethylenediamine. The sorption rate and capacity of themodified copolymer, p(GME)-en for Rh(III) Au(III) and Pt(IV) ions were determined in batch experiments under non-competitive conditions. The uptake of Rh(III) was faster than those ofAu(III) and Pt(IV). The sorption capacity for Pt(IV)was determined in the pHrange 0.9–6.0. The maximum Pt(IV) uptake capacity onto p(GME)-en at pH 5.5 was 1.30 mmol/g., Umreženi makroporozni poli(glicidilmetakrilat-ko-etilenglikoldimetakrilat) sintetizovan je suspenzionom kopolimerizacijom i modifikovan reakcijom bočnih epoksidnih grupa sa etilendiaminom. Brzina sorpcije i kapacitet modifikovanog kopolimera, poli(GME)-en, za sorpciju Rh(III), Au(III) i Pt(IV) jona određeni su šaržnim eksperimentima pri nekompetitivnim uslovima. Utvrđeno je da je sorpcija Rh(III) jona na poli(GME)-en brža od sorpcije Au(III) i Pt(IV) jona. Kapacitet sorpcije Pt(IV) jona određen je u opsegu pH 0,9 – 6,0. Maksimalna količina Pt(IV) jona vezanih za p(GME)-en pri pH 5,5 iznosi 1,30 mmol/g.",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Noble metal binding on macroporous poly(GMA-co-EGDMA) modified with ethylenediamine, Vezivanje plemenitih metala za makroporozni poli(GMA-co-EGDMA)kopolimer modifikovan sa etilendiaminom",
volume = "69",
number = "6",
pages = "455-460",
doi = "10.2298/JSC0406455N"
}
Nastasović, A., Jovanović, S. M., Jakovljević, D., Stanković, S.,& Onjia, A. E.. (2004). Noble metal binding on macroporous poly(GMA-co-EGDMA) modified with ethylenediamine. in Journal of the Serbian Chemical Society
Serbian Chemical Society., 69(6), 455-460.
https://doi.org/10.2298/JSC0406455N
Nastasović A, Jovanović SM, Jakovljević D, Stanković S, Onjia AE. Noble metal binding on macroporous poly(GMA-co-EGDMA) modified with ethylenediamine. in Journal of the Serbian Chemical Society. 2004;69(6):455-460.
doi:10.2298/JSC0406455N .
Nastasović, Aleksandra, Jovanović, Slobodan M., Jakovljević, Dragica, Stanković, Slavka, Onjia, Antonije E., "Noble metal binding on macroporous poly(GMA-co-EGDMA) modified with ethylenediamine" in Journal of the Serbian Chemical Society, 69, no. 6 (2004):455-460,
https://doi.org/10.2298/JSC0406455N . .
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The behavior of polypyrrole doped with different anions as an ion‐selective electrode

Jovanović, Vladislava M.; Markičević, Ljiljana; Stanković, Slavka; Stanković, Rade; Jovanović, Momir S.

(Wiley, 1995)

TY  - JOUR
AU  - Jovanović, Vladislava M.
AU  - Markičević, Ljiljana
AU  - Stanković, Slavka
AU  - Stanković, Rade
AU  - Jovanović, Momir S.
PY  - 1995
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/3668
AB  - Polypyrrole (PPy) films were electrochemically deposited on glassy carbon from aqueous solutions of different sodium salts (F−, Cl−, NO 3−, HSO 4−). Methods applied were potentiostatic polymerization or cyclic voltammetry. The electrochemical behavior of such electrodes was studied by cyclic voltammetry. The results obtained show that the reaction is localized at the electrode surface for polypyrrole doped with CI− and NO 3−, anions and diffusion‐controlled for F− anions. The polypyrrole films, examined as ion‐selective electrodes in solutions of anions corresponding to the dopant ones, exhibit lower or higher deviation from the Nernstian response depending on the dopant. When polypyrrole doped with HSO 4− was tested, a cationic response was obtained. The chemical exchange process of dopant anion was studied. The results show that this process depends on the nature of the dopant anion and the anion from the solution.
PB  - Wiley
T2  - Electroanalysis
T1  - The behavior of polypyrrole doped with different anions as an ion‐selective electrode
VL  - 7
IS  - 6
SP  - 574
EP  - 578
DO  - 10.1002/elan.1140070613
ER  - 
@article{
author = "Jovanović, Vladislava M. and Markičević, Ljiljana and Stanković, Slavka and Stanković, Rade and Jovanović, Momir S.",
year = "1995",
abstract = "Polypyrrole (PPy) films were electrochemically deposited on glassy carbon from aqueous solutions of different sodium salts (F−, Cl−, NO 3−, HSO 4−). Methods applied were potentiostatic polymerization or cyclic voltammetry. The electrochemical behavior of such electrodes was studied by cyclic voltammetry. The results obtained show that the reaction is localized at the electrode surface for polypyrrole doped with CI− and NO 3−, anions and diffusion‐controlled for F− anions. The polypyrrole films, examined as ion‐selective electrodes in solutions of anions corresponding to the dopant ones, exhibit lower or higher deviation from the Nernstian response depending on the dopant. When polypyrrole doped with HSO 4− was tested, a cationic response was obtained. The chemical exchange process of dopant anion was studied. The results show that this process depends on the nature of the dopant anion and the anion from the solution.",
publisher = "Wiley",
journal = "Electroanalysis",
title = "The behavior of polypyrrole doped with different anions as an ion‐selective electrode",
volume = "7",
number = "6",
pages = "574-578",
doi = "10.1002/elan.1140070613"
}
Jovanović, V. M., Markičević, L., Stanković, S., Stanković, R.,& Jovanović, M. S.. (1995). The behavior of polypyrrole doped with different anions as an ion‐selective electrode. in Electroanalysis
Wiley., 7(6), 574-578.
https://doi.org/10.1002/elan.1140070613
Jovanović VM, Markičević L, Stanković S, Stanković R, Jovanović MS. The behavior of polypyrrole doped with different anions as an ion‐selective electrode. in Electroanalysis. 1995;7(6):574-578.
doi:10.1002/elan.1140070613 .
Jovanović, Vladislava M., Markičević, Ljiljana, Stanković, Slavka, Stanković, Rade, Jovanović, Momir S., "The behavior of polypyrrole doped with different anions as an ion‐selective electrode" in Electroanalysis, 7, no. 6 (1995):574-578,
https://doi.org/10.1002/elan.1140070613 . .
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