Krstić, Jugoslav

Link to this page

Authority KeyName Variants
orcid::0000-0003-0321-0698
  • Krstić, Jugoslav (9)
Projects
Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 200023 (Institute of Technology of Nuclear and Other Mineral Row Materials - ITNMS, Belgrade) Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 200026 (University of Belgrade, Institute of Chemistry, Technology and Metallurgy - IChTM)
Oxide-based environmentally-friendly porous materials for genotoxic substances removal Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 200161 (University of Belgrade, Faculty of Pharmacy)
CEEPUS III network [CIII-CZ-0212-05-1112] CEEPUS II network [CII-CZ-0212-04-1011]
European Union [HU-SRB/0901/121/116 OCE-EFPTRWR] info:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172057
Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 200043 (Institute of Oncology and Radiology of Serbia, Belgrade) Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 200146 (University of Belgrade, Faculty of Physical Chemistry)
Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 200175 (Institute of Technical Sciences of SASA, Belgrade) Nanostructured Functional and Composite Materials in Catalytic and Sorption Processes
Vaskularni zid, faktori rizika i oksidativni stres: od molekula do fiziološke osnove prevencije i terapije Development of technological processes for obtaining of ecological materials based on nonmetallic minerals
Development of micro- and nanosystems as carriers for drugs with anti-inflammatory effect and methods for their characterization Ministry of Education and Science of Serbia
Secretariat for Science and Technological Development of AP Vojvodina, Republic of Serbia [114-451-02011/2007-02

Author's Bibliography

Bentonite Modified with Surfactants—Efficient Adsorbents for the Removal of Non-Steroidal Anti-Inflammatory Drugs

Obradović, Milena; Daković, Aleksandra; Smiljanić, Danijela; Marković, Marija; Ožegović, Milica; Krstić, Jugoslav; Vuković, Nikola; Milojević-Rakić, Maja

(MDPI, 2024)

TY  - JOUR
AU  - Obradović, Milena
AU  - Daković, Aleksandra
AU  - Smiljanić, Danijela
AU  - Marković, Marija
AU  - Ožegović, Milica
AU  - Krstić, Jugoslav
AU  - Vuković, Nikola
AU  - Milojević-Rakić, Maja
PY  - 2024
UR  - https://ritnms.itnms.ac.rs/handle/123456789/1222
AB  - Organobentonites have been applied for the removal of two common non-steroidal anti-inflammatory drugs, ibuprofen (IBU) and diclofenac sodium (DS), from aqueous solutions. Two surfactants, one with and the other without benzyl group (octadecyldimethylbenzylammonium chloride, ODMBA, and hexadecyltrimethylammonium bromide, HDTMA), in amounts equivalent to 50, 75, and 100% of the cation exchange capacity of bentonite were used for the preparation of organobentonites. Successful modification of bentonite was confirmed by several methods: X-ray powder diffraction (XRPD), point of the zero charge (pHPZC), determination of exchanged inorganic cations in bentonite, determination of textural properties, and scanning electron microscopy (SEM). Kinetic and thermodynamic data on the adsorption of IBU and DS showed that drug adsorption was controlled by the type and the amount of surfactant incorporated into the bentonite and by their arrangement in the interlayer space and at the surface of organobentonites. The adsorption of both drugs increased with an increase in the amount of both surfactants in organobentonites. The presence of the benzyl group in organobentonites enhanced the adsorption of IBU and DS and was more pronounced for IBU. Drug adsorption fits the pseudo-second-order kinetic model the best. The thermodynamic data revealed that the adsorption process was endothermic in nature and with increase of the amount of both surfactants drug adsorption processes were more spontaneous. The results obtained from this study revealed that adsorbents based on surfactants modified bentonite are promising candidates for IBU and DS removal from contaminated water.
PB  - MDPI
T2  - Processes
T1  - Bentonite Modified with Surfactants—Efficient Adsorbents for the Removal of Non-Steroidal Anti-Inflammatory Drugs
IS  - 1
SP  - 96
VL  - 12
DO  - 10.3390/pr12010096
ER  - 
@article{
author = "Obradović, Milena and Daković, Aleksandra and Smiljanić, Danijela and Marković, Marija and Ožegović, Milica and Krstić, Jugoslav and Vuković, Nikola and Milojević-Rakić, Maja",
year = "2024",
abstract = "Organobentonites have been applied for the removal of two common non-steroidal anti-inflammatory drugs, ibuprofen (IBU) and diclofenac sodium (DS), from aqueous solutions. Two surfactants, one with and the other without benzyl group (octadecyldimethylbenzylammonium chloride, ODMBA, and hexadecyltrimethylammonium bromide, HDTMA), in amounts equivalent to 50, 75, and 100% of the cation exchange capacity of bentonite were used for the preparation of organobentonites. Successful modification of bentonite was confirmed by several methods: X-ray powder diffraction (XRPD), point of the zero charge (pHPZC), determination of exchanged inorganic cations in bentonite, determination of textural properties, and scanning electron microscopy (SEM). Kinetic and thermodynamic data on the adsorption of IBU and DS showed that drug adsorption was controlled by the type and the amount of surfactant incorporated into the bentonite and by their arrangement in the interlayer space and at the surface of organobentonites. The adsorption of both drugs increased with an increase in the amount of both surfactants in organobentonites. The presence of the benzyl group in organobentonites enhanced the adsorption of IBU and DS and was more pronounced for IBU. Drug adsorption fits the pseudo-second-order kinetic model the best. The thermodynamic data revealed that the adsorption process was endothermic in nature and with increase of the amount of both surfactants drug adsorption processes were more spontaneous. The results obtained from this study revealed that adsorbents based on surfactants modified bentonite are promising candidates for IBU and DS removal from contaminated water.",
publisher = "MDPI",
journal = "Processes",
title = "Bentonite Modified with Surfactants—Efficient Adsorbents for the Removal of Non-Steroidal Anti-Inflammatory Drugs",
number = "1",
pages = "96",
volume = "12",
doi = "10.3390/pr12010096"
}
Obradović, M., Daković, A., Smiljanić, D., Marković, M., Ožegović, M., Krstić, J., Vuković, N.,& Milojević-Rakić, M.. (2024). Bentonite Modified with Surfactants—Efficient Adsorbents for the Removal of Non-Steroidal Anti-Inflammatory Drugs. in Processes
MDPI., 12(1), 96.
https://doi.org/10.3390/pr12010096
Obradović M, Daković A, Smiljanić D, Marković M, Ožegović M, Krstić J, Vuković N, Milojević-Rakić M. Bentonite Modified with Surfactants—Efficient Adsorbents for the Removal of Non-Steroidal Anti-Inflammatory Drugs. in Processes. 2024;12(1):96.
doi:10.3390/pr12010096 .
Obradović, Milena, Daković, Aleksandra, Smiljanić, Danijela, Marković, Marija, Ožegović, Milica, Krstić, Jugoslav, Vuković, Nikola, Milojević-Rakić, Maja, "Bentonite Modified with Surfactants—Efficient Adsorbents for the Removal of Non-Steroidal Anti-Inflammatory Drugs" in Processes, 12, no. 1 (2024):96,
https://doi.org/10.3390/pr12010096 . .

Oxide Powder Mixture with Poly-vinyl Alcohol (PVA) and added Polyethylene Glycol (PEG) as Plasticizer

Labus, Nebojsa; Krstić, Jugoslav; Matijašević, Srđan; Pavlović, Vladimir

(Belgrade : Association for ETRAN Society, 2023)

TY  - JOUR
AU  - Labus, Nebojsa
AU  - Krstić, Jugoslav
AU  - Matijašević, Srđan
AU  - Pavlović, Vladimir
PY  - 2023
UR  - https://ritnms.itnms.ac.rs/handle/123456789/743
AB  - Powder mixture consisted of ZnO, Mn2O3 (MnCO3) and Fe2O3 blended powders, was found laminating during compaction. Polyvinyl alcohol (PVA) and a combination of PVA with polyethylene glycol (PEG) added as a plasticizer, were introduced as polymer binders to improve the compaction of oxide mixtures. It has been done by forming a suspension of oxide mixture and varying the polymer solution concentration and composition. By evaporating the solvent, new materials were obtained, which consist of oxide particles bound via polymer. In such a manner obtained hybrid materials were characterized with attenuated total reflection Fourier transformed infrared (ATR-FTIR) spectroscopy, differential thermal analysis (DTA) and transmission electron microscopy (TEM). The oxide polymer material was compacted at 200 MPa and the expansion of this compact during heating was monitored in temperature range up to 550ºC with dilatometer. It was found that PVA forms graft polymer with PEG and specific interaction with oxide particles surface was revealed.
AB  - Смеша прахова састављена од ZnO, Mn2O3 (MnCO3) и Fe2O3 комбинације
прахова је показивала ламинацију током пресовања. Поливинил алкохол (PVA) и
комбинација PVA са полиетилен гликолом (PEG) који је додат као пластификатор, су
уведени као полимерно везиво за пресовање оксидних прахова. Везиво је уведено тако
што је формирана суспензија смеше различитих оксида прахова у полимерном
раствору. Концентрације полимера и састави су варирани. Уклањањем растварача
добијени су нови материјали који се састоје од честица оксида повезаних полимерима.
Ови хибридни материјали окарактерисани су методама ометене тоталне рефлексије
фурије трансформисане инфрацрвене спектроскопије (ATR-FTIR) као и
диференцијалне термичке анализе (DTA). Микроструктура је посматрана
трансмисоном електронском микроскопијом (TEM). Оксид-полимер материјали су
пресовани на притиску од 200 MPa и ширење испреска током грејања је праћено у температурском опсегу од собне до 550ºC употребом дилатометра. Нађено је да PVA
формира графт полимер са PEG и да постоји специфична интеракција полимера са
површином честица оксида.
PB  - Belgrade : Association for ETRAN Society
T2  - Science of Sintering
T1  - Oxide Powder Mixture with Poly-vinyl Alcohol (PVA) and added Polyethylene Glycol (PEG) as Plasticizer
EP  - 2023
SP  - 189
VL  - 55
DO  - 10.2298/SOS220828005L
ER  - 
@article{
author = "Labus, Nebojsa and Krstić, Jugoslav and Matijašević, Srđan and Pavlović, Vladimir",
year = "2023",
abstract = "Powder mixture consisted of ZnO, Mn2O3 (MnCO3) and Fe2O3 blended powders, was found laminating during compaction. Polyvinyl alcohol (PVA) and a combination of PVA with polyethylene glycol (PEG) added as a plasticizer, were introduced as polymer binders to improve the compaction of oxide mixtures. It has been done by forming a suspension of oxide mixture and varying the polymer solution concentration and composition. By evaporating the solvent, new materials were obtained, which consist of oxide particles bound via polymer. In such a manner obtained hybrid materials were characterized with attenuated total reflection Fourier transformed infrared (ATR-FTIR) spectroscopy, differential thermal analysis (DTA) and transmission electron microscopy (TEM). The oxide polymer material was compacted at 200 MPa and the expansion of this compact during heating was monitored in temperature range up to 550ºC with dilatometer. It was found that PVA forms graft polymer with PEG and specific interaction with oxide particles surface was revealed., Смеша прахова састављена од ZnO, Mn2O3 (MnCO3) и Fe2O3 комбинације
прахова је показивала ламинацију током пресовања. Поливинил алкохол (PVA) и
комбинација PVA са полиетилен гликолом (PEG) који је додат као пластификатор, су
уведени као полимерно везиво за пресовање оксидних прахова. Везиво је уведено тако
што је формирана суспензија смеше различитих оксида прахова у полимерном
раствору. Концентрације полимера и састави су варирани. Уклањањем растварача
добијени су нови материјали који се састоје од честица оксида повезаних полимерима.
Ови хибридни материјали окарактерисани су методама ометене тоталне рефлексије
фурије трансформисане инфрацрвене спектроскопије (ATR-FTIR) као и
диференцијалне термичке анализе (DTA). Микроструктура је посматрана
трансмисоном електронском микроскопијом (TEM). Оксид-полимер материјали су
пресовани на притиску од 200 MPa и ширење испреска током грејања је праћено у температурском опсегу од собне до 550ºC употребом дилатометра. Нађено је да PVA
формира графт полимер са PEG и да постоји специфична интеракција полимера са
површином честица оксида.",
publisher = "Belgrade : Association for ETRAN Society",
journal = "Science of Sintering",
title = "Oxide Powder Mixture with Poly-vinyl Alcohol (PVA) and added Polyethylene Glycol (PEG) as Plasticizer",
pages = "2023-189",
volume = "55",
doi = "10.2298/SOS220828005L"
}
Labus, N., Krstić, J., Matijašević, S.,& Pavlović, V.. (2023). Oxide Powder Mixture with Poly-vinyl Alcohol (PVA) and added Polyethylene Glycol (PEG) as Plasticizer. in Science of Sintering
Belgrade : Association for ETRAN Society., 55, 189-2023.
https://doi.org/10.2298/SOS220828005L
Labus N, Krstić J, Matijašević S, Pavlović V. Oxide Powder Mixture with Poly-vinyl Alcohol (PVA) and added Polyethylene Glycol (PEG) as Plasticizer. in Science of Sintering. 2023;55:189-2023.
doi:10.2298/SOS220828005L .
Labus, Nebojsa, Krstić, Jugoslav, Matijašević, Srđan, Pavlović, Vladimir, "Oxide Powder Mixture with Poly-vinyl Alcohol (PVA) and added Polyethylene Glycol (PEG) as Plasticizer" in Science of Sintering, 55 (2023):189-2023,
https://doi.org/10.2298/SOS220828005L . .

Ibuprofen and diclofenac sodium adsorption onto functionalized minerals: Equilibrium, kinetic and thermodynamic studies

Obradović, Milena; Daković, Aleksandra; Smiljanić, Danijela; Ožegović, Milica; Marković, Marija; Rottinghaus, George E.; Krstić, Jugoslav

(Elsevier, Amsterdam, 2022)

TY  - JOUR
AU  - Obradović, Milena
AU  - Daković, Aleksandra
AU  - Smiljanić, Danijela
AU  - Ožegović, Milica
AU  - Marković, Marija
AU  - Rottinghaus, George E.
AU  - Krstić, Jugoslav
PY  - 2022
UR  - https://ritnms.itnms.ac.rs/handle/123456789/643
AB  - Cationic surfactant - octadecyldimethylbenzyl ammonium chloride (ODMBA) was used for modification of the three natural raw materials - bentonite, kaolin and zeolite. Adsorption of ODMBA by minerals occurred via ion exchange of inorganic cations on minerals with surfactant. Organomodified minerals - organobentonite (OB), organokaolin (OK) and organozeolite (OZ) were studied as adsorbents for removal of two non-steroidal anti-inflammatory drugs - ibuprofen (IBU) and diclofenac sodium (DS) at pH 7. For all systems, the pseudo-second order model showed the best correlation to kinetic experimental data. In all cases, the positive values of Delta H degrees indicated that the adsorption of both IBU and DS by organomodified minerals was endothermic in nature. Equilibrium data were better described by the Freundlich isotherm model, pointing to adsorbent heterogeneous active sites for adsorption. Under applied experimental conditions, the highest adsorption of both drugs was achieved by OB, while much lower capacities were observed for OK and OZ. Nonlinear isotherms and physicochemical characterization of organomodified minerals after drugs adsorption suggested complex mechanism consisting of hydrophobic interactions between hydrophobic part of the drugs and surfactants alkyl chains, electrostatic interactions of anionic forms of IBU and DS with the cationic "head" of ODMBA, as well as anion exchange of counterion ions from ODMBA micelle and anionic forms of both drugs. Adsorption of both IBU and DS was strongly dependent on the amount of ODMBA ions in the minerals.
PB  - Elsevier, Amsterdam
T2  - Microporous and Mesoporous Materials
T1  - Ibuprofen and diclofenac sodium adsorption onto functionalized minerals: Equilibrium, kinetic and thermodynamic studies
VL  - 335
DO  - 10.1016/j.micromeso.2022.111795
UR  - conv_945
ER  - 
@article{
author = "Obradović, Milena and Daković, Aleksandra and Smiljanić, Danijela and Ožegović, Milica and Marković, Marija and Rottinghaus, George E. and Krstić, Jugoslav",
year = "2022",
abstract = "Cationic surfactant - octadecyldimethylbenzyl ammonium chloride (ODMBA) was used for modification of the three natural raw materials - bentonite, kaolin and zeolite. Adsorption of ODMBA by minerals occurred via ion exchange of inorganic cations on minerals with surfactant. Organomodified minerals - organobentonite (OB), organokaolin (OK) and organozeolite (OZ) were studied as adsorbents for removal of two non-steroidal anti-inflammatory drugs - ibuprofen (IBU) and diclofenac sodium (DS) at pH 7. For all systems, the pseudo-second order model showed the best correlation to kinetic experimental data. In all cases, the positive values of Delta H degrees indicated that the adsorption of both IBU and DS by organomodified minerals was endothermic in nature. Equilibrium data were better described by the Freundlich isotherm model, pointing to adsorbent heterogeneous active sites for adsorption. Under applied experimental conditions, the highest adsorption of both drugs was achieved by OB, while much lower capacities were observed for OK and OZ. Nonlinear isotherms and physicochemical characterization of organomodified minerals after drugs adsorption suggested complex mechanism consisting of hydrophobic interactions between hydrophobic part of the drugs and surfactants alkyl chains, electrostatic interactions of anionic forms of IBU and DS with the cationic "head" of ODMBA, as well as anion exchange of counterion ions from ODMBA micelle and anionic forms of both drugs. Adsorption of both IBU and DS was strongly dependent on the amount of ODMBA ions in the minerals.",
publisher = "Elsevier, Amsterdam",
journal = "Microporous and Mesoporous Materials",
title = "Ibuprofen and diclofenac sodium adsorption onto functionalized minerals: Equilibrium, kinetic and thermodynamic studies",
volume = "335",
doi = "10.1016/j.micromeso.2022.111795",
url = "conv_945"
}
Obradović, M., Daković, A., Smiljanić, D., Ožegović, M., Marković, M., Rottinghaus, G. E.,& Krstić, J.. (2022). Ibuprofen and diclofenac sodium adsorption onto functionalized minerals: Equilibrium, kinetic and thermodynamic studies. in Microporous and Mesoporous Materials
Elsevier, Amsterdam., 335.
https://doi.org/10.1016/j.micromeso.2022.111795
conv_945
Obradović M, Daković A, Smiljanić D, Ožegović M, Marković M, Rottinghaus GE, Krstić J. Ibuprofen and diclofenac sodium adsorption onto functionalized minerals: Equilibrium, kinetic and thermodynamic studies. in Microporous and Mesoporous Materials. 2022;335.
doi:10.1016/j.micromeso.2022.111795
conv_945 .
Obradović, Milena, Daković, Aleksandra, Smiljanić, Danijela, Ožegović, Milica, Marković, Marija, Rottinghaus, George E., Krstić, Jugoslav, "Ibuprofen and diclofenac sodium adsorption onto functionalized minerals: Equilibrium, kinetic and thermodynamic studies" in Microporous and Mesoporous Materials, 335 (2022),
https://doi.org/10.1016/j.micromeso.2022.111795 .,
conv_945 .
18
17

Influence of selective acid-etching on functionality of halloysite-chitosan nanocontainers for sustained drug release

Jauković, Valentina; Krajišnik, Danina; Daković, Aleksandra; Damjanović, Ana; Krstić, Jugoslav; Stojanović, Jovica; Calija, Bojan

(Elsevier, Amsterdam, 2021)

TY  - JOUR
AU  - Jauković, Valentina
AU  - Krajišnik, Danina
AU  - Daković, Aleksandra
AU  - Damjanović, Ana
AU  - Krstić, Jugoslav
AU  - Stojanović, Jovica
AU  - Calija, Bojan
PY  - 2021
UR  - https://ritnms.itnms.ac.rs/handle/123456789/598
AB  - The functionality of halloysite (Hal) nanotubes as drug carriers can be improved by lumen enlargement and polymer modification. This study investigates the influence of selective acid etching on Hal functionalization with cationic biopolymer chitosan. Hal was subjected to lumen etching under mild conditions, loaded under vacuum with nonsteroidal antiinflammatory drug aceclofenac, and incubated in an acidic solution of chitosan. The functionality of pristine and etched Hal before and upon polymer functionalization was assessed by ?-potential measurements, structural characterization (FT-IR, DSC and XRPD analysis), cell viability assay, drug loading and drug release studies. Acid etching increased specific surface area, pore volume and pore size of Hal, decreased ?-potential and facilitated binding of the cationic polymer. XRPD and DSC analysis revealed crystalline structure of etched Hal. Successful chitosan binding and drug entrapment were further confirmed by FT-IR and DSC studies. XRPD showed surface polymer binding. DSC and FT-IR analyses confirmed the presence of the entrapped drug in its crystalline form. Drug loading was increased for ?81% by selective lumen etching. Slight decrease of drug content occurred during chitosan functionalization due to aceclofenac diffusion in the polymer solution. The drug release was more sustained from etched Hal nanocomposites (up to ?87% for 12 h) than from pristine Hal (up to ?97% for 12 h) due to more intensive chitosan binding. High human fibroblast survival rates upon exposure to pristine and etched Hal before and after chitosan functionalization (>90% in the concentration of 1000 ?g/mL) confirmed that both lumen etching under mild conditions and polymer functionalization had no significant effect on cytocompatibility. Based on these findings, selective lumen etching in combination with polycation modification appears to be a promising approach for improvement of Hal nanotubes functionality by increasing payload, polymer binding capacity, and sustained release properties with no significant effect on their cytocompatibility.
PB  - Elsevier, Amsterdam
T2  - Materials Science & Engineering C-Materials for Biological Applications
T1  - Influence of selective acid-etching on functionality of halloysite-chitosan nanocontainers for sustained drug release
VL  - 123
DO  - 10.1016/j.msec.2021.112029
UR  - conv_907
ER  - 
@article{
author = "Jauković, Valentina and Krajišnik, Danina and Daković, Aleksandra and Damjanović, Ana and Krstić, Jugoslav and Stojanović, Jovica and Calija, Bojan",
year = "2021",
abstract = "The functionality of halloysite (Hal) nanotubes as drug carriers can be improved by lumen enlargement and polymer modification. This study investigates the influence of selective acid etching on Hal functionalization with cationic biopolymer chitosan. Hal was subjected to lumen etching under mild conditions, loaded under vacuum with nonsteroidal antiinflammatory drug aceclofenac, and incubated in an acidic solution of chitosan. The functionality of pristine and etched Hal before and upon polymer functionalization was assessed by ?-potential measurements, structural characterization (FT-IR, DSC and XRPD analysis), cell viability assay, drug loading and drug release studies. Acid etching increased specific surface area, pore volume and pore size of Hal, decreased ?-potential and facilitated binding of the cationic polymer. XRPD and DSC analysis revealed crystalline structure of etched Hal. Successful chitosan binding and drug entrapment were further confirmed by FT-IR and DSC studies. XRPD showed surface polymer binding. DSC and FT-IR analyses confirmed the presence of the entrapped drug in its crystalline form. Drug loading was increased for ?81% by selective lumen etching. Slight decrease of drug content occurred during chitosan functionalization due to aceclofenac diffusion in the polymer solution. The drug release was more sustained from etched Hal nanocomposites (up to ?87% for 12 h) than from pristine Hal (up to ?97% for 12 h) due to more intensive chitosan binding. High human fibroblast survival rates upon exposure to pristine and etched Hal before and after chitosan functionalization (>90% in the concentration of 1000 ?g/mL) confirmed that both lumen etching under mild conditions and polymer functionalization had no significant effect on cytocompatibility. Based on these findings, selective lumen etching in combination with polycation modification appears to be a promising approach for improvement of Hal nanotubes functionality by increasing payload, polymer binding capacity, and sustained release properties with no significant effect on their cytocompatibility.",
publisher = "Elsevier, Amsterdam",
journal = "Materials Science & Engineering C-Materials for Biological Applications",
title = "Influence of selective acid-etching on functionality of halloysite-chitosan nanocontainers for sustained drug release",
volume = "123",
doi = "10.1016/j.msec.2021.112029",
url = "conv_907"
}
Jauković, V., Krajišnik, D., Daković, A., Damjanović, A., Krstić, J., Stojanović, J.,& Calija, B.. (2021). Influence of selective acid-etching on functionality of halloysite-chitosan nanocontainers for sustained drug release. in Materials Science & Engineering C-Materials for Biological Applications
Elsevier, Amsterdam., 123.
https://doi.org/10.1016/j.msec.2021.112029
conv_907
Jauković V, Krajišnik D, Daković A, Damjanović A, Krstić J, Stojanović J, Calija B. Influence of selective acid-etching on functionality of halloysite-chitosan nanocontainers for sustained drug release. in Materials Science & Engineering C-Materials for Biological Applications. 2021;123.
doi:10.1016/j.msec.2021.112029
conv_907 .
Jauković, Valentina, Krajišnik, Danina, Daković, Aleksandra, Damjanović, Ana, Krstić, Jugoslav, Stojanović, Jovica, Calija, Bojan, "Influence of selective acid-etching on functionality of halloysite-chitosan nanocontainers for sustained drug release" in Materials Science & Engineering C-Materials for Biological Applications, 123 (2021),
https://doi.org/10.1016/j.msec.2021.112029 .,
conv_907 .
20
2
21

Influence of surface coverage of kaolin with surfactant ions on adsorption of ochratoxin A and zearalenone

Spasojević, Milica; Daković, Aleksandra; Rottinghaus, George E.; Obradović, Milena; Krajišnik, Danina; Marković, Marija; Krstić, Jugoslav

(Elsevier, Amsterdam, 2021)

TY  - JOUR
AU  - Spasojević, Milica
AU  - Daković, Aleksandra
AU  - Rottinghaus, George E.
AU  - Obradović, Milena
AU  - Krajišnik, Danina
AU  - Marković, Marija
AU  - Krstić, Jugoslav
PY  - 2021
UR  - https://ritnms.itnms.ac.rs/handle/123456789/573
AB  - A natural kaolin from Serbia was modified with different amounts of octadecyldimethylbenzyl ammonium (ODMBA) - (25, 50 and 90% of kaolin cation exchange capacity). Samples were denoted as OKR-25, OKR-50 and OKR-90. Several methods (FTIR spectroscopy, thermal analysis, zeta potential measurements, and N2 physisorption) were used for characterization of the organokaolinites. Adsorption of the common mycotoxins ochratoxin A (OCHRA) and zearalenone (ZEN) by the organokaolinites was investigated at different levels of solid phase in suspension, different initial mycotoxin concentrations and different pH values. The natural kaolin was not effective in binding OCHRA or ZEN. Adsorption of both mycotoxins by organokaolinites increased with increasing amounts of solid phase as well as with increasing levels of surfactant on the kaolin surface. OCHRA and ZEN adsorption by all organokaolinites followed non-linear adsorption isotherms, at pH 3, 7 and 9. The maximum adsorption capacity for OCHRA adsorption was at pH 3 (4.8 mg/g for OKR-25, 26.7 mg/g for OKR-50 and 39.2 mg/g for OKR-90) that was calculated from the Langmuir model. Much lower OCHRA adsorption capacities were found at pH 7 and 9 (from 0.8 mg/g to 6.9 mg/g at pH 7 and from 1.1 mg/g to 4.6 mg/g at pH 9). The following adsorption capacities for ZEN were obtained from the Langmuir isotherms, at pH 3: 4.5 mg/g for OKR-25, 12.0 mg/g for OKR-50 and 13.5 mg/g for OKR-90. At pH 7, adsorption of ZEN was 5.7 mg/g for OKR25, 15.3 mg/g for OKR-90 and 14. 4 mg/g for OKR-90. At pH 9, ZEN adsorption capacities were 2.4, 14.1 and 8.1 mg/g for OKR-25, OKR-50 and OKR-90, respectively. Thus, at the lowest amount of ODMBA at the kaolin surface, adsorption of ZEN was similar at pH 3 and 7, while a slightly lower value was obtained for its adsorption at pH 9. With increasing amounts of organic phase at the kaolin surface, the adsorption of ZEN was practically independent of pH. Adsorption of both mycotoxins was dependent on the amount of ODMBA ions at the kaolin surface as well as on their forms in solution.
PB  - Elsevier, Amsterdam
T2  - Applied Clay Science
T1  - Influence of surface coverage of kaolin with surfactant ions on adsorption of ochratoxin A and zearalenone
VL  - 205
DO  - 10.1016/j.clay.2021.106040
UR  - conv_909
ER  - 
@article{
author = "Spasojević, Milica and Daković, Aleksandra and Rottinghaus, George E. and Obradović, Milena and Krajišnik, Danina and Marković, Marija and Krstić, Jugoslav",
year = "2021",
abstract = "A natural kaolin from Serbia was modified with different amounts of octadecyldimethylbenzyl ammonium (ODMBA) - (25, 50 and 90% of kaolin cation exchange capacity). Samples were denoted as OKR-25, OKR-50 and OKR-90. Several methods (FTIR spectroscopy, thermal analysis, zeta potential measurements, and N2 physisorption) were used for characterization of the organokaolinites. Adsorption of the common mycotoxins ochratoxin A (OCHRA) and zearalenone (ZEN) by the organokaolinites was investigated at different levels of solid phase in suspension, different initial mycotoxin concentrations and different pH values. The natural kaolin was not effective in binding OCHRA or ZEN. Adsorption of both mycotoxins by organokaolinites increased with increasing amounts of solid phase as well as with increasing levels of surfactant on the kaolin surface. OCHRA and ZEN adsorption by all organokaolinites followed non-linear adsorption isotherms, at pH 3, 7 and 9. The maximum adsorption capacity for OCHRA adsorption was at pH 3 (4.8 mg/g for OKR-25, 26.7 mg/g for OKR-50 and 39.2 mg/g for OKR-90) that was calculated from the Langmuir model. Much lower OCHRA adsorption capacities were found at pH 7 and 9 (from 0.8 mg/g to 6.9 mg/g at pH 7 and from 1.1 mg/g to 4.6 mg/g at pH 9). The following adsorption capacities for ZEN were obtained from the Langmuir isotherms, at pH 3: 4.5 mg/g for OKR-25, 12.0 mg/g for OKR-50 and 13.5 mg/g for OKR-90. At pH 7, adsorption of ZEN was 5.7 mg/g for OKR25, 15.3 mg/g for OKR-90 and 14. 4 mg/g for OKR-90. At pH 9, ZEN adsorption capacities were 2.4, 14.1 and 8.1 mg/g for OKR-25, OKR-50 and OKR-90, respectively. Thus, at the lowest amount of ODMBA at the kaolin surface, adsorption of ZEN was similar at pH 3 and 7, while a slightly lower value was obtained for its adsorption at pH 9. With increasing amounts of organic phase at the kaolin surface, the adsorption of ZEN was practically independent of pH. Adsorption of both mycotoxins was dependent on the amount of ODMBA ions at the kaolin surface as well as on their forms in solution.",
publisher = "Elsevier, Amsterdam",
journal = "Applied Clay Science",
title = "Influence of surface coverage of kaolin with surfactant ions on adsorption of ochratoxin A and zearalenone",
volume = "205",
doi = "10.1016/j.clay.2021.106040",
url = "conv_909"
}
Spasojević, M., Daković, A., Rottinghaus, G. E., Obradović, M., Krajišnik, D., Marković, M.,& Krstić, J.. (2021). Influence of surface coverage of kaolin with surfactant ions on adsorption of ochratoxin A and zearalenone. in Applied Clay Science
Elsevier, Amsterdam., 205.
https://doi.org/10.1016/j.clay.2021.106040
conv_909
Spasojević M, Daković A, Rottinghaus GE, Obradović M, Krajišnik D, Marković M, Krstić J. Influence of surface coverage of kaolin with surfactant ions on adsorption of ochratoxin A and zearalenone. in Applied Clay Science. 2021;205.
doi:10.1016/j.clay.2021.106040
conv_909 .
Spasojević, Milica, Daković, Aleksandra, Rottinghaus, George E., Obradović, Milena, Krajišnik, Danina, Marković, Marija, Krstić, Jugoslav, "Influence of surface coverage of kaolin with surfactant ions on adsorption of ochratoxin A and zearalenone" in Applied Clay Science, 205 (2021),
https://doi.org/10.1016/j.clay.2021.106040 .,
conv_909 .
4
2
6

Waste Slag from Heating Plants as a Partial Replacement for Cement in Mortar and Concrete Production. Part I-Physical-Chemical and Physical-Mechanical Characterization of Slag

Nedeljković, Andrijana; Stojmenović, Marija; Gulicovski, Jelena; Ristić, Nenad; Milićević, Sonja; Krstić, Jugoslav; Kragović, Milan

(MDPI, Basel, 2020)

TY  - JOUR
AU  - Nedeljković, Andrijana
AU  - Stojmenović, Marija
AU  - Gulicovski, Jelena
AU  - Ristić, Nenad
AU  - Milićević, Sonja
AU  - Krstić, Jugoslav
AU  - Kragović, Milan
PY  - 2020
UR  - https://ritnms.itnms.ac.rs/handle/123456789/543
AB  - Numerous factors influence the complexity of environmental and waste management problems, and the most significant goal is the reuse of materials that have completed their "life cycle" and the reduction in the use of new resources. In order to reduce impact of waste slag on the environment, in the present study, waste slag, generated in heating plants after lignite combustion, was characterized in detail and tested for application as a replacement for cement in mortar or concrete production. For physical-chemical characterization of slag, different experimental and instrumental techniques were used such as chemical composition and determination of the content of heavy metals, investigation of morphological and textural properties, thermal analysis, X-ray, and infrared spectroscopy. Physical-mechanical characterization of slag was also performed and included determination of activity index, water requirement, setting time and soundness. A leaching test was also performed. Presented results show that waste slag may be used in mortar and concrete production as a partial cement replacement, but after additional combustion at 650 degrees C and partial replacement of slag with silica fume in the minimal amount of 12%. The maximal obtained cement replacement was 20% (17.8% slag and 2.2% of silica fume).
PB  - MDPI, Basel
T2  - Minerals
T1  - Waste Slag from Heating Plants as a Partial Replacement for Cement in Mortar and Concrete Production. Part I-Physical-Chemical and Physical-Mechanical Characterization of Slag
IS  - 11
VL  - 10
DO  - 10.3390/min10110992
UR  - conv_896
ER  - 
@article{
author = "Nedeljković, Andrijana and Stojmenović, Marija and Gulicovski, Jelena and Ristić, Nenad and Milićević, Sonja and Krstić, Jugoslav and Kragović, Milan",
year = "2020",
abstract = "Numerous factors influence the complexity of environmental and waste management problems, and the most significant goal is the reuse of materials that have completed their "life cycle" and the reduction in the use of new resources. In order to reduce impact of waste slag on the environment, in the present study, waste slag, generated in heating plants after lignite combustion, was characterized in detail and tested for application as a replacement for cement in mortar or concrete production. For physical-chemical characterization of slag, different experimental and instrumental techniques were used such as chemical composition and determination of the content of heavy metals, investigation of morphological and textural properties, thermal analysis, X-ray, and infrared spectroscopy. Physical-mechanical characterization of slag was also performed and included determination of activity index, water requirement, setting time and soundness. A leaching test was also performed. Presented results show that waste slag may be used in mortar and concrete production as a partial cement replacement, but after additional combustion at 650 degrees C and partial replacement of slag with silica fume in the minimal amount of 12%. The maximal obtained cement replacement was 20% (17.8% slag and 2.2% of silica fume).",
publisher = "MDPI, Basel",
journal = "Minerals",
title = "Waste Slag from Heating Plants as a Partial Replacement for Cement in Mortar and Concrete Production. Part I-Physical-Chemical and Physical-Mechanical Characterization of Slag",
number = "11",
volume = "10",
doi = "10.3390/min10110992",
url = "conv_896"
}
Nedeljković, A., Stojmenović, M., Gulicovski, J., Ristić, N., Milićević, S., Krstić, J.,& Kragović, M.. (2020). Waste Slag from Heating Plants as a Partial Replacement for Cement in Mortar and Concrete Production. Part I-Physical-Chemical and Physical-Mechanical Characterization of Slag. in Minerals
MDPI, Basel., 10(11).
https://doi.org/10.3390/min10110992
conv_896
Nedeljković A, Stojmenović M, Gulicovski J, Ristić N, Milićević S, Krstić J, Kragović M. Waste Slag from Heating Plants as a Partial Replacement for Cement in Mortar and Concrete Production. Part I-Physical-Chemical and Physical-Mechanical Characterization of Slag. in Minerals. 2020;10(11).
doi:10.3390/min10110992
conv_896 .
Nedeljković, Andrijana, Stojmenović, Marija, Gulicovski, Jelena, Ristić, Nenad, Milićević, Sonja, Krstić, Jugoslav, Kragović, Milan, "Waste Slag from Heating Plants as a Partial Replacement for Cement in Mortar and Concrete Production. Part I-Physical-Chemical and Physical-Mechanical Characterization of Slag" in Minerals, 10, no. 11 (2020),
https://doi.org/10.3390/min10110992 .,
conv_896 .
8
2
8

Inorganically modified diatomite as a potential prolonged-release drug carrier

Janićijević, Jelena; Krajišnik, Danina; Calija, Bojan; Dobričić, Vladimir; Daković, Aleksandra; Krstić, Jugoslav; Marković, Marija; Milić, Jela

(Elsevier, Amsterdam, 2014)

TY  - JOUR
AU  - Janićijević, Jelena
AU  - Krajišnik, Danina
AU  - Calija, Bojan
AU  - Dobričić, Vladimir
AU  - Daković, Aleksandra
AU  - Krstić, Jugoslav
AU  - Marković, Marija
AU  - Milić, Jela
PY  - 2014
UR  - https://ritnms.itnms.ac.rs/handle/123456789/321
AB  - Inorganic modification of diatomite was performed with the precipitation product of partially neutralized aluminum sulfate solution at three different mass ratios. The starting and the modified diatomites were characterized by SEM-EDS, FTIR, thermal analysis and zeta potential measurements and evaluated for drug loading capacity in adsorption batch experiments using diclofenac sodium (DS) as a model drug. In vitro drug release studies were performed in phosphate buffer pH 6.8 from comprimates containing: the drug adsorbed onto the selected modified diatomite sample (DAMD), physical mixture of the drug with the selected modified diatomite sample (PMDMD) and physical mixture of the drug with the starting diatomite (PMDD). In vivo acute toxicity testing of the modified diatomite samples was performed on mice. High adsorbent loading of the selected modified diatomite sample (similar to 250 mg/g in 2 h) enabled the preparation of comprimates containing adsorbed DS in the amount near to its therapeutic dose. Drug release studies demonstrated prolonged release of DS over a period of 8 h from both DAMD comprimates (18% after 8 h) and PMDMD comprimates (45% after 8 h). The release kinetics for DAMD and PMDMD comprimates fitted well with Korsmeyer-Peppas and Bhaskar models, indicating that the release mechanism was a combination of non-Fickian diffusion and ion exchange process.
PB  - Elsevier, Amsterdam
T2  - Materials Science & Engineering C-Materials for Biological Applications
T1  - Inorganically modified diatomite as a potential prolonged-release drug carrier
EP  - 420
SP  - 412
VL  - 42
DO  - 10.1016/j.msec.2014.05.052
UR  - conv_701
ER  - 
@article{
author = "Janićijević, Jelena and Krajišnik, Danina and Calija, Bojan and Dobričić, Vladimir and Daković, Aleksandra and Krstić, Jugoslav and Marković, Marija and Milić, Jela",
year = "2014",
abstract = "Inorganic modification of diatomite was performed with the precipitation product of partially neutralized aluminum sulfate solution at three different mass ratios. The starting and the modified diatomites were characterized by SEM-EDS, FTIR, thermal analysis and zeta potential measurements and evaluated for drug loading capacity in adsorption batch experiments using diclofenac sodium (DS) as a model drug. In vitro drug release studies were performed in phosphate buffer pH 6.8 from comprimates containing: the drug adsorbed onto the selected modified diatomite sample (DAMD), physical mixture of the drug with the selected modified diatomite sample (PMDMD) and physical mixture of the drug with the starting diatomite (PMDD). In vivo acute toxicity testing of the modified diatomite samples was performed on mice. High adsorbent loading of the selected modified diatomite sample (similar to 250 mg/g in 2 h) enabled the preparation of comprimates containing adsorbed DS in the amount near to its therapeutic dose. Drug release studies demonstrated prolonged release of DS over a period of 8 h from both DAMD comprimates (18% after 8 h) and PMDMD comprimates (45% after 8 h). The release kinetics for DAMD and PMDMD comprimates fitted well with Korsmeyer-Peppas and Bhaskar models, indicating that the release mechanism was a combination of non-Fickian diffusion and ion exchange process.",
publisher = "Elsevier, Amsterdam",
journal = "Materials Science & Engineering C-Materials for Biological Applications",
title = "Inorganically modified diatomite as a potential prolonged-release drug carrier",
pages = "420-412",
volume = "42",
doi = "10.1016/j.msec.2014.05.052",
url = "conv_701"
}
Janićijević, J., Krajišnik, D., Calija, B., Dobričić, V., Daković, A., Krstić, J., Marković, M.,& Milić, J.. (2014). Inorganically modified diatomite as a potential prolonged-release drug carrier. in Materials Science & Engineering C-Materials for Biological Applications
Elsevier, Amsterdam., 42, 412-420.
https://doi.org/10.1016/j.msec.2014.05.052
conv_701
Janićijević J, Krajišnik D, Calija B, Dobričić V, Daković A, Krstić J, Marković M, Milić J. Inorganically modified diatomite as a potential prolonged-release drug carrier. in Materials Science & Engineering C-Materials for Biological Applications. 2014;42:412-420.
doi:10.1016/j.msec.2014.05.052
conv_701 .
Janićijević, Jelena, Krajišnik, Danina, Calija, Bojan, Dobričić, Vladimir, Daković, Aleksandra, Krstić, Jugoslav, Marković, Marija, Milić, Jela, "Inorganically modified diatomite as a potential prolonged-release drug carrier" in Materials Science & Engineering C-Materials for Biological Applications, 42 (2014):412-420,
https://doi.org/10.1016/j.msec.2014.05.052 .,
conv_701 .
25
16
29

Renewable silver-amalgam film electrode for voltammetric monitoring of solar photodegradation of imidacloprid in the presence of Fe/TiO2 and TiO2 catalysts

Guzsvany, Valeria; Petrović, Jelena; Krstić, Jugoslav; Papp, Zsigmond; Putek, Maria; Bjelica, Luka; Bobrowski, Andrzej; Abramović, Biljana

(Elsevier Science Sa, Lausanne, 2013)

TY  - JOUR
AU  - Guzsvany, Valeria
AU  - Petrović, Jelena
AU  - Krstić, Jugoslav
AU  - Papp, Zsigmond
AU  - Putek, Maria
AU  - Bjelica, Luka
AU  - Bobrowski, Andrzej
AU  - Abramović, Biljana
PY  - 2013
UR  - https://ritnms.itnms.ac.rs/handle/123456789/250
AB  - A rapid and sensitive voltammetric method has been developed for the characterization and determination of the imidacloprid insecticide by means of square-wave voltammetry (SWV) with a silver-amalgam film electrode (Hg(Ag)FE) in the aqueous Britton-Robinson buffer solution as the supporting electrolyte. In the investigated pH range between 2.0 and 9.0 two reduction peaks of imidacloprid were observed, and they were both obtained in a fairly negative potential range, (approximately from -0.8 to -1.5 V). Their shape strongly depended on the pH of the supporting electrolyte. The analytical measurements, based on the first peak, were performed at the pH of 7.0, and imidacloprid was determined in the concentration range of 0.91-47.48 mu g cm(-3). The reproducibility of the analytical signal was characterized by a relative standard deviation smaller than 1.0%, and the calculated values of detection and quantitation limits were 0.27 mu g cm(-3) and 0.91 mu g cm(-3), respectively. The applicability of the elaborated SWV method was tested by monitoring imidacloprid concentration during its solar photolytic and photocatalytic degradation in the presence of two heterogeneous catalysts: TiO2 and TiO2 modified with 1.9% w/w Fe (1.9% Fe/TiO2). Under photolytic conditions, imidacloprid degraded very slowly, and the presence of TiO2 as a catalyst accelerated the process, while 1.9% Fe/TiO2 showed a remarkable efficiency in the removal of imidacloprid under natural insolation. In all investigated cases the results obtained using the Hg(Ag)FE-SWV method were in agreement with those obtained by means of the comparative HPLC-DAD method, which confirmed that the developed voltammetric method can be used to monitor the degradation of imidacloprid.
PB  - Elsevier Science Sa, Lausanne
T2  - Journal of Electroanalytical Chemistry
T1  - Renewable silver-amalgam film electrode for voltammetric monitoring of solar photodegradation of imidacloprid in the presence of Fe/TiO2 and TiO2 catalysts
EP  - 39
SP  - 33
VL  - 699
DO  - 10.1016/j.jelechem.2013.04.003
UR  - conv_658
ER  - 
@article{
author = "Guzsvany, Valeria and Petrović, Jelena and Krstić, Jugoslav and Papp, Zsigmond and Putek, Maria and Bjelica, Luka and Bobrowski, Andrzej and Abramović, Biljana",
year = "2013",
abstract = "A rapid and sensitive voltammetric method has been developed for the characterization and determination of the imidacloprid insecticide by means of square-wave voltammetry (SWV) with a silver-amalgam film electrode (Hg(Ag)FE) in the aqueous Britton-Robinson buffer solution as the supporting electrolyte. In the investigated pH range between 2.0 and 9.0 two reduction peaks of imidacloprid were observed, and they were both obtained in a fairly negative potential range, (approximately from -0.8 to -1.5 V). Their shape strongly depended on the pH of the supporting electrolyte. The analytical measurements, based on the first peak, were performed at the pH of 7.0, and imidacloprid was determined in the concentration range of 0.91-47.48 mu g cm(-3). The reproducibility of the analytical signal was characterized by a relative standard deviation smaller than 1.0%, and the calculated values of detection and quantitation limits were 0.27 mu g cm(-3) and 0.91 mu g cm(-3), respectively. The applicability of the elaborated SWV method was tested by monitoring imidacloprid concentration during its solar photolytic and photocatalytic degradation in the presence of two heterogeneous catalysts: TiO2 and TiO2 modified with 1.9% w/w Fe (1.9% Fe/TiO2). Under photolytic conditions, imidacloprid degraded very slowly, and the presence of TiO2 as a catalyst accelerated the process, while 1.9% Fe/TiO2 showed a remarkable efficiency in the removal of imidacloprid under natural insolation. In all investigated cases the results obtained using the Hg(Ag)FE-SWV method were in agreement with those obtained by means of the comparative HPLC-DAD method, which confirmed that the developed voltammetric method can be used to monitor the degradation of imidacloprid.",
publisher = "Elsevier Science Sa, Lausanne",
journal = "Journal of Electroanalytical Chemistry",
title = "Renewable silver-amalgam film electrode for voltammetric monitoring of solar photodegradation of imidacloprid in the presence of Fe/TiO2 and TiO2 catalysts",
pages = "39-33",
volume = "699",
doi = "10.1016/j.jelechem.2013.04.003",
url = "conv_658"
}
Guzsvany, V., Petrović, J., Krstić, J., Papp, Z., Putek, M., Bjelica, L., Bobrowski, A.,& Abramović, B.. (2013). Renewable silver-amalgam film electrode for voltammetric monitoring of solar photodegradation of imidacloprid in the presence of Fe/TiO2 and TiO2 catalysts. in Journal of Electroanalytical Chemistry
Elsevier Science Sa, Lausanne., 699, 33-39.
https://doi.org/10.1016/j.jelechem.2013.04.003
conv_658
Guzsvany V, Petrović J, Krstić J, Papp Z, Putek M, Bjelica L, Bobrowski A, Abramović B. Renewable silver-amalgam film electrode for voltammetric monitoring of solar photodegradation of imidacloprid in the presence of Fe/TiO2 and TiO2 catalysts. in Journal of Electroanalytical Chemistry. 2013;699:33-39.
doi:10.1016/j.jelechem.2013.04.003
conv_658 .
Guzsvany, Valeria, Petrović, Jelena, Krstić, Jugoslav, Papp, Zsigmond, Putek, Maria, Bjelica, Luka, Bobrowski, Andrzej, Abramović, Biljana, "Renewable silver-amalgam film electrode for voltammetric monitoring of solar photodegradation of imidacloprid in the presence of Fe/TiO2 and TiO2 catalysts" in Journal of Electroanalytical Chemistry, 699 (2013):33-39,
https://doi.org/10.1016/j.jelechem.2013.04.003 .,
conv_658 .
34
29
33

Characterization of lead sorption by the natural and Fe(III)-modified zeolite

Kragović, Milan; Daković, Aleksandra; Marković, Marija; Krstić, Jugoslav; Gatta, G. Diego; Rotiroti, Nicola

(Elsevier, Amsterdam, 2013)

TY  - JOUR
AU  - Kragović, Milan
AU  - Daković, Aleksandra
AU  - Marković, Marija
AU  - Krstić, Jugoslav
AU  - Gatta, G. Diego
AU  - Rotiroti, Nicola
PY  - 2013
UR  - https://ritnms.itnms.ac.rs/handle/123456789/259
AB  - The influence of contact time, temperature and particle size on lead sorption by the natural and Fe(III)-modified zeolites was investigated. Characterization of the natural and Fe(III)-modified zeolite before and after lead sorption was performed by determination of textural properties, by scanning electron microscopy and X-ray spectroscopy in energy-dispersive mode (SEM-EDS), transmission electron microscopy (TEM) and X-ray powder diffraction (XRPD) analysis. Lead sorption kinetics at 303-333 K, best represented by the pseudo-second order model and activation energy (13.5 and 8.5 kJ/mol for the natural and Fe(III)-modified zeolite respectively) confirmed an activated chemical sorption. Desorption experiments indicated that lead was irreversibly sorbed on both zeolites. XRPD, TEM and SEM results showed that modification of the natural zeolite with Fe(III) ions did not change its crystal structure and iron is mainly located at the zeolite surface, likely in form of amorphous iron oxy-hydroxides. Specific surface area significantly increases after modification of the natural zeolite with Fe(III) ions (from 30.2 for the natural to 52.5 m(2)/g for Fe(III)-modified zeolite). Characterization of both lead saturated sorbents suggested that besides ion exchange, lead is both chemisorbed and precipitated at their surfaces, and presence of amorphous iron in Fe(III)-modified zeolite favors sorption of lead.
PB  - Elsevier, Amsterdam
T2  - Applied Surface Science
T1  - Characterization of lead sorption by the natural and Fe(III)-modified zeolite
EP  - 774
SP  - 764
VL  - 283
DO  - 10.1016/j.apsusc.2013.07.016
UR  - conv_664
ER  - 
@article{
author = "Kragović, Milan and Daković, Aleksandra and Marković, Marija and Krstić, Jugoslav and Gatta, G. Diego and Rotiroti, Nicola",
year = "2013",
abstract = "The influence of contact time, temperature and particle size on lead sorption by the natural and Fe(III)-modified zeolites was investigated. Characterization of the natural and Fe(III)-modified zeolite before and after lead sorption was performed by determination of textural properties, by scanning electron microscopy and X-ray spectroscopy in energy-dispersive mode (SEM-EDS), transmission electron microscopy (TEM) and X-ray powder diffraction (XRPD) analysis. Lead sorption kinetics at 303-333 K, best represented by the pseudo-second order model and activation energy (13.5 and 8.5 kJ/mol for the natural and Fe(III)-modified zeolite respectively) confirmed an activated chemical sorption. Desorption experiments indicated that lead was irreversibly sorbed on both zeolites. XRPD, TEM and SEM results showed that modification of the natural zeolite with Fe(III) ions did not change its crystal structure and iron is mainly located at the zeolite surface, likely in form of amorphous iron oxy-hydroxides. Specific surface area significantly increases after modification of the natural zeolite with Fe(III) ions (from 30.2 for the natural to 52.5 m(2)/g for Fe(III)-modified zeolite). Characterization of both lead saturated sorbents suggested that besides ion exchange, lead is both chemisorbed and precipitated at their surfaces, and presence of amorphous iron in Fe(III)-modified zeolite favors sorption of lead.",
publisher = "Elsevier, Amsterdam",
journal = "Applied Surface Science",
title = "Characterization of lead sorption by the natural and Fe(III)-modified zeolite",
pages = "774-764",
volume = "283",
doi = "10.1016/j.apsusc.2013.07.016",
url = "conv_664"
}
Kragović, M., Daković, A., Marković, M., Krstić, J., Gatta, G. D.,& Rotiroti, N.. (2013). Characterization of lead sorption by the natural and Fe(III)-modified zeolite. in Applied Surface Science
Elsevier, Amsterdam., 283, 764-774.
https://doi.org/10.1016/j.apsusc.2013.07.016
conv_664
Kragović M, Daković A, Marković M, Krstić J, Gatta GD, Rotiroti N. Characterization of lead sorption by the natural and Fe(III)-modified zeolite. in Applied Surface Science. 2013;283:764-774.
doi:10.1016/j.apsusc.2013.07.016
conv_664 .
Kragović, Milan, Daković, Aleksandra, Marković, Marija, Krstić, Jugoslav, Gatta, G. Diego, Rotiroti, Nicola, "Characterization of lead sorption by the natural and Fe(III)-modified zeolite" in Applied Surface Science, 283 (2013):764-774,
https://doi.org/10.1016/j.apsusc.2013.07.016 .,
conv_664 .
120
91
121