TY  - JOUR
AU  - Popović, Daniela
AU  - Stupar, G.
AU  - Miladinović, Jelena
AU  - Todorović, M.
AU  - Zrilić, Milorad
PY  - 2011
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1898
AB  - The solubility in the ternary system, aqueous mixture of CaSO4 and Na2SO4, at T = 298.15 K comprises five different salts: calcium sulfate dihydrate, mirabilite, thenardite, glauberite and labile salt. Using the Extended Pitzer's Ion Interaction model for pure and mixed electrolyte solutions and criteria of phase equilibria, predicted solubility behavior of salts was compared with experimental results from literature. The agreement between calculated and experimental solubilities was excellent in the ionic strength range up to 10.9062 mol kg(-1).
PB  - Maik Nauka/Interperiodica/Springer, New York
T2  - Russian Journal of Physical Chemistry A
T1  - Solubility in the ternary system CaSO4 + Na2SO4 + H2O at 298.15 K
EP  - 2353
IS  - 13
SP  - 2349
VL  - 85
DO  - 10.1134/S0036024411130255
ER  - 

@article{
author = "Popović, Daniela and Stupar, G. and Miladinović, Jelena and Todorović, M. and Zrilić, Milorad",
year = "2011",
abstract = "The solubility in the ternary system, aqueous mixture of CaSO4 and Na2SO4, at T = 298.15 K comprises five different salts: calcium sulfate dihydrate, mirabilite, thenardite, glauberite and labile salt. Using the Extended Pitzer's Ion Interaction model for pure and mixed electrolyte solutions and criteria of phase equilibria, predicted solubility behavior of salts was compared with experimental results from literature. The agreement between calculated and experimental solubilities was excellent in the ionic strength range up to 10.9062 mol kg(-1).",
publisher = "Maik Nauka/Interperiodica/Springer, New York",
journal = "Russian Journal of Physical Chemistry A",
title = "Solubility in the ternary system CaSO4 + Na2SO4 + H2O at 298.15 K",
pages = "2353-2349",
number = "13",
volume = "85",
doi = "10.1134/S0036024411130255"
}

Popović, D., Stupar, G., Miladinović, J., Todorović, M.,& Zrilić, M.. (2011). Solubility in the ternary system CaSO4 + Na2SO4 + H2O at 298.15 K. in Russian Journal of Physical Chemistry A
Maik Nauka/Interperiodica/Springer, New York., 85(13), 2349-2353.
https://doi.org/10.1134/S0036024411130255

Popović D, Stupar G, Miladinović J, Todorović M, Zrilić M. Solubility in the ternary system CaSO4 + Na2SO4 + H2O at 298.15 K. in Russian Journal of Physical Chemistry A. 2011;85(13):2349-2353.
doi:10.1134/S0036024411130255 .

Popović, Daniela, Stupar, G., Miladinović, Jelena, Todorović, M., Zrilić, Milorad, "Solubility in the ternary system CaSO4 + Na2SO4 + H2O at 298.15 K" in Russian Journal of Physical Chemistry A, 85, no. 13 (2011):2349-2353,
https://doi.org/10.1134/S0036024411130255 . .

TY  - JOUR
AU  - Radonjić, L.
AU  - Todorović, M.
AU  - Miladinović, Jelena
PY  - 2008
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1259
AB  - Ferroelectric nanostructured barium titanate (BT) thin films derived by a modified sol-gel process were formed by a deep coating method on Si (100) substrate. In this work was investigated the influence of different types and amounts of water (free water directly added in process and crystalline water from barium precursors) and of different barium precursors (hydroxide and acetate) on the gel-structure evolution and the barium titanate thin film crystallization. The IR-spectroscopy and X-ray diffraction analysis were used for sample characterization. Experimental results show that crystalline water from barium hydroxide octahydrate stabilizes the cubic phase of barium titanate. Barium titanate crystallizes in the tetragonal form in thin films when sols were prepared with free water and Ba-acetate or Ba-hydroxide monohydrate as precursors. The type of Ba-precursor used in preparation of sols effects the rate of crystallization of the BT in thin films, making it slower in the case when as precursor was used Ba-acetate than Ba-hydroxides. The prepared BT-thin films demonstrated good adhesion towards substrate and were smooth and uniform.
PB  - Springer, New York
T2  - Journal of Sol-Gel Science and Technology
T1  - Structural evolution of nanostructured barium titanate thin film sol-gel derived
EP  - 132
IS  - 2
SP  - 125
VL  - 45
DO  - 10.1007/s10971-007-1664-1
ER  - 

@article{
author = "Radonjić, L. and Todorović, M. and Miladinović, Jelena",
year = "2008",
abstract = "Ferroelectric nanostructured barium titanate (BT) thin films derived by a modified sol-gel process were formed by a deep coating method on Si (100) substrate. In this work was investigated the influence of different types and amounts of water (free water directly added in process and crystalline water from barium precursors) and of different barium precursors (hydroxide and acetate) on the gel-structure evolution and the barium titanate thin film crystallization. The IR-spectroscopy and X-ray diffraction analysis were used for sample characterization. Experimental results show that crystalline water from barium hydroxide octahydrate stabilizes the cubic phase of barium titanate. Barium titanate crystallizes in the tetragonal form in thin films when sols were prepared with free water and Ba-acetate or Ba-hydroxide monohydrate as precursors. The type of Ba-precursor used in preparation of sols effects the rate of crystallization of the BT in thin films, making it slower in the case when as precursor was used Ba-acetate than Ba-hydroxides. The prepared BT-thin films demonstrated good adhesion towards substrate and were smooth and uniform.",
publisher = "Springer, New York",
journal = "Journal of Sol-Gel Science and Technology",
title = "Structural evolution of nanostructured barium titanate thin film sol-gel derived",
pages = "132-125",
number = "2",
volume = "45",
doi = "10.1007/s10971-007-1664-1"
}

Radonjić, L., Todorović, M.,& Miladinović, J.. (2008). Structural evolution of nanostructured barium titanate thin film sol-gel derived. in Journal of Sol-Gel Science and Technology
Springer, New York., 45(2), 125-132.
https://doi.org/10.1007/s10971-007-1664-1

Radonjić L, Todorović M, Miladinović J. Structural evolution of nanostructured barium titanate thin film sol-gel derived. in Journal of Sol-Gel Science and Technology. 2008;45(2):125-132.
doi:10.1007/s10971-007-1664-1 .

Radonjić, L., Todorović, M., Miladinović, Jelena, "Structural evolution of nanostructured barium titanate thin film sol-gel derived" in Journal of Sol-Gel Science and Technology, 45, no. 2 (2008):125-132,
https://doi.org/10.1007/s10971-007-1664-1 . .

TY  - JOUR
AU  - Radonjić, L.
AU  - Todorović, M.
AU  - Miladinović, Jelena
PY  - 2005
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/825
AB  - Transparent, nanostructured glass ceramics based on ferroelectric solid solutions of the type Na1-xLixNbO3 (in very narrow composition regions for x=0.12 and 0.93) and LiNb1-yTayO3 (y=0.5 unlimited solid solubility), can be obtained by controlled crystallization of glass. The parent glass samples were prepared by conventional melt-quenching technique. Heat-treatment of the parent glasses was performed at the various temperatures, for the same time. The glass structure evolution during the controlled crystallization was examined by FT-IR spectroscopy analysis. Crystalline phases were identified by X-ray diffraction analysis and SEM was used for microstructure characterization. Densities of the crystallized glasses were measured by Archimedean principle. The capacitance and dielectric loss tangent were measured at a frequency of 1 kHz, at the room temperature. It was found that in the all investigated systems crystallize solid solutions Na1-xLixNbO3 and LiNb1-yTayO3 in the glassy matrix, have crystal size on nanoscale (less than 100nm), which is one of requirements to get a transparent glass ceramic that could be a good ferroelectric material regarding to the measured properties.
PB  - Elsevier Science Sa, Lausanne
T2  - Materials Science and Engineering B-Solid State Materials for Advanced Technology
T1  - Nanostructured sodium lithium niobate and lithium niobium tantalate solid solutions obtained by controlled crystallization of glass
EP  - 70
IS  - 1-2
SP  - 64
VL  - 121
DO  - 10.1016/j.mseb.2005.03.003
ER  - 

@article{
author = "Radonjić, L. and Todorović, M. and Miladinović, Jelena",
year = "2005",
abstract = "Transparent, nanostructured glass ceramics based on ferroelectric solid solutions of the type Na1-xLixNbO3 (in very narrow composition regions for x=0.12 and 0.93) and LiNb1-yTayO3 (y=0.5 unlimited solid solubility), can be obtained by controlled crystallization of glass. The parent glass samples were prepared by conventional melt-quenching technique. Heat-treatment of the parent glasses was performed at the various temperatures, for the same time. The glass structure evolution during the controlled crystallization was examined by FT-IR spectroscopy analysis. Crystalline phases were identified by X-ray diffraction analysis and SEM was used for microstructure characterization. Densities of the crystallized glasses were measured by Archimedean principle. The capacitance and dielectric loss tangent were measured at a frequency of 1 kHz, at the room temperature. It was found that in the all investigated systems crystallize solid solutions Na1-xLixNbO3 and LiNb1-yTayO3 in the glassy matrix, have crystal size on nanoscale (less than 100nm), which is one of requirements to get a transparent glass ceramic that could be a good ferroelectric material regarding to the measured properties.",
publisher = "Elsevier Science Sa, Lausanne",
journal = "Materials Science and Engineering B-Solid State Materials for Advanced Technology",
title = "Nanostructured sodium lithium niobate and lithium niobium tantalate solid solutions obtained by controlled crystallization of glass",
pages = "70-64",
number = "1-2",
volume = "121",
doi = "10.1016/j.mseb.2005.03.003"
}

Radonjić, L., Todorović, M.,& Miladinović, J.. (2005). Nanostructured sodium lithium niobate and lithium niobium tantalate solid solutions obtained by controlled crystallization of glass. in Materials Science and Engineering B-Solid State Materials for Advanced Technology
Elsevier Science Sa, Lausanne., 121(1-2), 64-70.
https://doi.org/10.1016/j.mseb.2005.03.003

Radonjić L, Todorović M, Miladinović J. Nanostructured sodium lithium niobate and lithium niobium tantalate solid solutions obtained by controlled crystallization of glass. in Materials Science and Engineering B-Solid State Materials for Advanced Technology. 2005;121(1-2):64-70.
doi:10.1016/j.mseb.2005.03.003 .

Radonjić, L., Todorović, M., Miladinović, Jelena, "Nanostructured sodium lithium niobate and lithium niobium tantalate solid solutions obtained by controlled crystallization of glass" in Materials Science and Engineering B-Solid State Materials for Advanced Technology, 121, no. 1-2 (2005):64-70,
https://doi.org/10.1016/j.mseb.2005.03.003 . .

TY  - JOUR
AU  - Radonjić, L.
AU  - Todorović, M..
AU  - Miladinović, Jelena
PY  - 2005
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/733
AB  - The subject of this work is the study of nanostructured sodium niobate obtained by a controlled crystallisation of glass. The glass samples of the composition within the system NaNbO3-SiO2-Al2O3 were prepared by melting and then crystallised by a heat treatment method at previously determined temperatures and times. Transparent, nanostructured glass ceramic, based on NaNbO3 crystals, was obtained. Infrared absorption spectroscopy analysis of the prepared glass samples shows that the sodium ions are situated in a glass network nearer to SiO4-tetrahedra than NbO6-octahedra. XRD analysis of the crystallised glass samples shows that phase separation precedes the nucleation of NaNbO3 in glass matrix.
T2  - Physics and Chemistry of Glasses
T1  - Glass formation and crystallisation behaviour of nanostructured sodium niobate by direct glass crystallisation
EP  - 203
IS  - 2
SP  - 201
VL  - 46
UR  - https://hdl.handle.net/21.15107/rcub_technorep_733
ER  - 

@article{
author = "Radonjić, L. and Todorović, M.. and Miladinović, Jelena",
year = "2005",
abstract = "The subject of this work is the study of nanostructured sodium niobate obtained by a controlled crystallisation of glass. The glass samples of the composition within the system NaNbO3-SiO2-Al2O3 were prepared by melting and then crystallised by a heat treatment method at previously determined temperatures and times. Transparent, nanostructured glass ceramic, based on NaNbO3 crystals, was obtained. Infrared absorption spectroscopy analysis of the prepared glass samples shows that the sodium ions are situated in a glass network nearer to SiO4-tetrahedra than NbO6-octahedra. XRD analysis of the crystallised glass samples shows that phase separation precedes the nucleation of NaNbO3 in glass matrix.",
journal = "Physics and Chemistry of Glasses",
title = "Glass formation and crystallisation behaviour of nanostructured sodium niobate by direct glass crystallisation",
pages = "203-201",
number = "2",
volume = "46",
url = "https://hdl.handle.net/21.15107/rcub_technorep_733"
}

Radonjić, L., Todorović, M..,& Miladinović, J.. (2005). Glass formation and crystallisation behaviour of nanostructured sodium niobate by direct glass crystallisation. in Physics and Chemistry of Glasses, 46(2), 201-203.
https://hdl.handle.net/21.15107/rcub_technorep_733

Radonjić L, Todorović M, Miladinović J. Glass formation and crystallisation behaviour of nanostructured sodium niobate by direct glass crystallisation. in Physics and Chemistry of Glasses. 2005;46(2):201-203.
https://hdl.handle.net/21.15107/rcub_technorep_733 .

Radonjić, L., Todorović, M.., Miladinović, Jelena, "Glass formation and crystallisation behaviour of nanostructured sodium niobate by direct glass crystallisation" in Physics and Chemistry of Glasses, 46, no. 2 (2005):201-203,
https://hdl.handle.net/21.15107/rcub_technorep_733 .

TY  - JOUR
AU  - Radonjić, L.
AU  - Todorović, M.
AU  - Miladinović, Jelena
PY  - 2005
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/732
AB  - The influence of various processing parameters is investigated during sol formation (metal precursors: titanium (IV) butoxide, barium hydroxide, barium acetate; pH of sol solution; type and amount of stabiliser and solvent; amount of water) and on the properties of the resulting gel. A relationship is established between sol-gel structure and the temperatures of BaTiO3 crystallisation and the structured evolution of layers deposited on the substrate Si (100). Experiments revealed the stable and suitable BaTiO3 Sol structures, responsible for low temperature crystallisation of BaTiO3. The IR, DTA and XRD analysis provide sample characterisation. The obtained results show that by using titanium (IV) butoxide and barium hydroxide monohydrate may be obtained a thin BaTiO3 layer at the low crystallisation temperatures, between 600 and 700 degrees C, with only the tetragonal phase of barium titanate present.
T2  - Physics and Chemistry of Glasses
T1  - Processing of ferroelectric thin layers of barium titanate by the sol-gel method
EP  - 214
IS  - 2
SP  - 211
VL  - 46
UR  - https://hdl.handle.net/21.15107/rcub_technorep_732
ER  - 

@article{
author = "Radonjić, L. and Todorović, M. and Miladinović, Jelena",
year = "2005",
abstract = "The influence of various processing parameters is investigated during sol formation (metal precursors: titanium (IV) butoxide, barium hydroxide, barium acetate; pH of sol solution; type and amount of stabiliser and solvent; amount of water) and on the properties of the resulting gel. A relationship is established between sol-gel structure and the temperatures of BaTiO3 crystallisation and the structured evolution of layers deposited on the substrate Si (100). Experiments revealed the stable and suitable BaTiO3 Sol structures, responsible for low temperature crystallisation of BaTiO3. The IR, DTA and XRD analysis provide sample characterisation. The obtained results show that by using titanium (IV) butoxide and barium hydroxide monohydrate may be obtained a thin BaTiO3 layer at the low crystallisation temperatures, between 600 and 700 degrees C, with only the tetragonal phase of barium titanate present.",
journal = "Physics and Chemistry of Glasses",
title = "Processing of ferroelectric thin layers of barium titanate by the sol-gel method",
pages = "214-211",
number = "2",
volume = "46",
url = "https://hdl.handle.net/21.15107/rcub_technorep_732"
}

Radonjić, L., Todorović, M.,& Miladinović, J.. (2005). Processing of ferroelectric thin layers of barium titanate by the sol-gel method. in Physics and Chemistry of Glasses, 46(2), 211-214.
https://hdl.handle.net/21.15107/rcub_technorep_732

Radonjić L, Todorović M, Miladinović J. Processing of ferroelectric thin layers of barium titanate by the sol-gel method. in Physics and Chemistry of Glasses. 2005;46(2):211-214.
https://hdl.handle.net/21.15107/rcub_technorep_732 .

Radonjić, L., Todorović, M., Miladinović, Jelena, "Processing of ferroelectric thin layers of barium titanate by the sol-gel method" in Physics and Chemistry of Glasses, 46, no. 2 (2005):211-214,
https://hdl.handle.net/21.15107/rcub_technorep_732 .

TY  - JOUR
AU  - Radonjić, L.
AU  - Todorović, M.
AU  - Miladinović, Jelena
PY  - 2004
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/700
AB  - The subject of this work was to obtain nanostructured sodium niobate crystals by a controlled crystallization method from glasses. The glass samples of the composition within the system NaNbO3-SiO2-Al2O3 were prepared by melting and then subjected to crystallization by heat treatment, at previously determined temperatures and times. Transparent, nanostructured glass-ceramics based on NaNbO3 crystals were obtained. FT IR-absorption spectroscopy has been used to interpret structural changes of the prepared glass samples during the heat treatment. XRD analysis of the crystallized glass samples shows that phase separation precedes the nucleation of NaNbO3 in glass matrix and the lowest temperature of the sodium niobate nucleation is 700degreesC. SEM analysis of the crystallized glasses shows that the crystal size of NaNbO3 was on nanoscale.
PB  - Elsevier Science Sa, Lausanne
T2  - Materials Chemistry and Physics
T1  - Nanostructured sodium niobate obtained by glass crystallization
EP  - 432
IS  - 2-3
SP  - 427
VL  - 88
DO  - 10.1016/j.matchemphys.2004.08.011
ER  - 

@article{
author = "Radonjić, L. and Todorović, M. and Miladinović, Jelena",
year = "2004",
abstract = "The subject of this work was to obtain nanostructured sodium niobate crystals by a controlled crystallization method from glasses. The glass samples of the composition within the system NaNbO3-SiO2-Al2O3 were prepared by melting and then subjected to crystallization by heat treatment, at previously determined temperatures and times. Transparent, nanostructured glass-ceramics based on NaNbO3 crystals were obtained. FT IR-absorption spectroscopy has been used to interpret structural changes of the prepared glass samples during the heat treatment. XRD analysis of the crystallized glass samples shows that phase separation precedes the nucleation of NaNbO3 in glass matrix and the lowest temperature of the sodium niobate nucleation is 700degreesC. SEM analysis of the crystallized glasses shows that the crystal size of NaNbO3 was on nanoscale.",
publisher = "Elsevier Science Sa, Lausanne",
journal = "Materials Chemistry and Physics",
title = "Nanostructured sodium niobate obtained by glass crystallization",
pages = "432-427",
number = "2-3",
volume = "88",
doi = "10.1016/j.matchemphys.2004.08.011"
}

Radonjić, L., Todorović, M.,& Miladinović, J.. (2004). Nanostructured sodium niobate obtained by glass crystallization. in Materials Chemistry and Physics
Elsevier Science Sa, Lausanne., 88(2-3), 427-432.
https://doi.org/10.1016/j.matchemphys.2004.08.011

Radonjić L, Todorović M, Miladinović J. Nanostructured sodium niobate obtained by glass crystallization. in Materials Chemistry and Physics. 2004;88(2-3):427-432.
doi:10.1016/j.matchemphys.2004.08.011 .

Radonjić, L., Todorović, M., Miladinović, Jelena, "Nanostructured sodium niobate obtained by glass crystallization" in Materials Chemistry and Physics, 88, no. 2-3 (2004):427-432,
https://doi.org/10.1016/j.matchemphys.2004.08.011 . .

TY  - JOUR
AU  - Miladinović, Jelena
AU  - Ninković, Rozalija
AU  - Todorović, M.
AU  - Jovanović, V
PY  - 2003
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/510
AB  - The osmotic coefficient of ZnCl2(aq) has been measured at T = 298.15 K by the isopiestic method over the range of molalities from (0.4 to 2.4) mol . kg(-1) with KCl(aq) as the reference solution. The available literature data on the osmotic coefficient of ZnCl2(aq) at T = 298.15 K, and new experimental data were treated by the Clegg-Pitzer-Brimblecombe equation and the extended Pitzer's equation. These equations were used to calculate the activity coefficient of ZnCl2 at T = 298.15 K. The formation of the ZnCl+ complex has been taken into account by means of the Clegg-Pitzer-Brimblecombe equation.
PB  - Academic Press Ltd- Elsevier Science Ltd, London
T2  - Journal of Chemical Thermodynamics
T1  - Osmotic coefficient of the ZnCl2(aq) at T=298.15 K
EP  - 1082
IS  - 7
SP  - 1073
VL  - 35
DO  - 10.1016/S0021-9614(03)00048-X
ER  - 

@article{
author = "Miladinović, Jelena and Ninković, Rozalija and Todorović, M. and Jovanović, V",
year = "2003",
abstract = "The osmotic coefficient of ZnCl2(aq) has been measured at T = 298.15 K by the isopiestic method over the range of molalities from (0.4 to 2.4) mol . kg(-1) with KCl(aq) as the reference solution. The available literature data on the osmotic coefficient of ZnCl2(aq) at T = 298.15 K, and new experimental data were treated by the Clegg-Pitzer-Brimblecombe equation and the extended Pitzer's equation. These equations were used to calculate the activity coefficient of ZnCl2 at T = 298.15 K. The formation of the ZnCl+ complex has been taken into account by means of the Clegg-Pitzer-Brimblecombe equation.",
publisher = "Academic Press Ltd- Elsevier Science Ltd, London",
journal = "Journal of Chemical Thermodynamics",
title = "Osmotic coefficient of the ZnCl2(aq) at T=298.15 K",
pages = "1082-1073",
number = "7",
volume = "35",
doi = "10.1016/S0021-9614(03)00048-X"
}

Miladinović, J., Ninković, R., Todorović, M.,& Jovanović, V.. (2003). Osmotic coefficient of the ZnCl2(aq) at T=298.15 K. in Journal of Chemical Thermodynamics
Academic Press Ltd- Elsevier Science Ltd, London., 35(7), 1073-1082.
https://doi.org/10.1016/S0021-9614(03)00048-X

Miladinović J, Ninković R, Todorović M, Jovanović V. Osmotic coefficient of the ZnCl2(aq) at T=298.15 K. in Journal of Chemical Thermodynamics. 2003;35(7):1073-1082.
doi:10.1016/S0021-9614(03)00048-X .

Miladinović, Jelena, Ninković, Rozalija, Todorović, M., Jovanović, V, "Osmotic coefficient of the ZnCl2(aq) at T=298.15 K" in Journal of Chemical Thermodynamics, 35, no. 7 (2003):1073-1082,
https://doi.org/10.1016/S0021-9614(03)00048-X . .

TY  - JOUR
AU  - Onjia, Antonije
AU  - Milonjić, Slobodan K.
AU  - Todorović, M.
AU  - Loos-Nesković, C
AU  - Fedoroff, M
AU  - Jones, DJ
PY  - 2002
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/443
AB  - The surface properties of Ni and Cu hexacyanoferrates were investigated by the inverse gas chromatography method. Retentions of 10 organic compounds were measured at zero surface coverage in the temperature range 80 to 95 C. The gas/solid partition coefficients and the related thermodynamic data of adsorption (standard free energy change, standard state enthalpies, and entropy changes) also at zero surface coverage were determined. The dispersive component of free surface energy of both hexacyanoferrates, at investigated temperatures, was calculated. The surface acid/base properties were also evaluated using polar adsorbates and the results obtained indicate that nickel hexacyanoferrate is more acidic than copper hexacyanoferrate.
PB  - Academic Press Inc Elsevier Science, San Diego
T2  - Journal of Colloid and Interface Science
T1  - An inverse gas chromatography study of the adsorption of organics on nickel- and copper-hexacyanoferrates at zero surface coverage
EP  - 17
IS  - 1
SP  - 10
VL  - 251
DO  - 10.1006/jcis.2002.8372
ER  - 

@article{
author = "Onjia, Antonije and Milonjić, Slobodan K. and Todorović, M. and Loos-Nesković, C and Fedoroff, M and Jones, DJ",
year = "2002",
abstract = "The surface properties of Ni and Cu hexacyanoferrates were investigated by the inverse gas chromatography method. Retentions of 10 organic compounds were measured at zero surface coverage in the temperature range 80 to 95 C. The gas/solid partition coefficients and the related thermodynamic data of adsorption (standard free energy change, standard state enthalpies, and entropy changes) also at zero surface coverage were determined. The dispersive component of free surface energy of both hexacyanoferrates, at investigated temperatures, was calculated. The surface acid/base properties were also evaluated using polar adsorbates and the results obtained indicate that nickel hexacyanoferrate is more acidic than copper hexacyanoferrate.",
publisher = "Academic Press Inc Elsevier Science, San Diego",
journal = "Journal of Colloid and Interface Science",
title = "An inverse gas chromatography study of the adsorption of organics on nickel- and copper-hexacyanoferrates at zero surface coverage",
pages = "17-10",
number = "1",
volume = "251",
doi = "10.1006/jcis.2002.8372"
}

Onjia, A., Milonjić, S. K., Todorović, M., Loos-Nesković, C., Fedoroff, M.,& Jones, D.. (2002). An inverse gas chromatography study of the adsorption of organics on nickel- and copper-hexacyanoferrates at zero surface coverage. in Journal of Colloid and Interface Science
Academic Press Inc Elsevier Science, San Diego., 251(1), 10-17.
https://doi.org/10.1006/jcis.2002.8372

Onjia A, Milonjić SK, Todorović M, Loos-Nesković C, Fedoroff M, Jones D. An inverse gas chromatography study of the adsorption of organics on nickel- and copper-hexacyanoferrates at zero surface coverage. in Journal of Colloid and Interface Science. 2002;251(1):10-17.
doi:10.1006/jcis.2002.8372 .

Onjia, Antonije, Milonjić, Slobodan K., Todorović, M., Loos-Nesković, C, Fedoroff, M, Jones, DJ, "An inverse gas chromatography study of the adsorption of organics on nickel- and copper-hexacyanoferrates at zero surface coverage" in Journal of Colloid and Interface Science, 251, no. 1 (2002):10-17,
https://doi.org/10.1006/jcis.2002.8372 . .

TY  - JOUR
AU  - Miladinović, Jelena
AU  - Todorović, M.
AU  - Ninković, Rozalija
PY  - 2002
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/435
AB  - The osmotic coefficient of ZnSO4(aq) has been measured at T = 298.15 K by the iso-piestic method, in the range of molalities from 1.3 to 3.0 mol . kg(-1), with KCl(aq) as the reference solution. Experimental data of osmotic coefficient were treated to determine the ionic interaction parameters in Pitzer's equation and equation of Clegg-Pitzer-Brimblecombe. These equations were used to calculate the activity coefficient of ZnSO4 at T = 298. 15 K.
PB  - Academic Press Ltd- Elsevier Science Ltd, London
T2  - Journal of Chemical Thermodynamics
T1  - Osmotic coefficient of the ZnSO4(aq) at T=298.15 K
EP  - 1776
IS  - 11
SP  - 1769
VL  - 34
DO  - 10.1016/S0021-9614(02)00164-7
ER  - 

@article{
author = "Miladinović, Jelena and Todorović, M. and Ninković, Rozalija",
year = "2002",
abstract = "The osmotic coefficient of ZnSO4(aq) has been measured at T = 298.15 K by the iso-piestic method, in the range of molalities from 1.3 to 3.0 mol . kg(-1), with KCl(aq) as the reference solution. Experimental data of osmotic coefficient were treated to determine the ionic interaction parameters in Pitzer's equation and equation of Clegg-Pitzer-Brimblecombe. These equations were used to calculate the activity coefficient of ZnSO4 at T = 298. 15 K.",
publisher = "Academic Press Ltd- Elsevier Science Ltd, London",
journal = "Journal of Chemical Thermodynamics",
title = "Osmotic coefficient of the ZnSO4(aq) at T=298.15 K",
pages = "1776-1769",
number = "11",
volume = "34",
doi = "10.1016/S0021-9614(02)00164-7"
}

Miladinović, J., Todorović, M.,& Ninković, R.. (2002). Osmotic coefficient of the ZnSO4(aq) at T=298.15 K. in Journal of Chemical Thermodynamics
Academic Press Ltd- Elsevier Science Ltd, London., 34(11), 1769-1776.
https://doi.org/10.1016/S0021-9614(02)00164-7

Miladinović J, Todorović M, Ninković R. Osmotic coefficient of the ZnSO4(aq) at T=298.15 K. in Journal of Chemical Thermodynamics. 2002;34(11):1769-1776.
doi:10.1016/S0021-9614(02)00164-7 .

Miladinović, Jelena, Todorović, M., Ninković, Rozalija, "Osmotic coefficient of the ZnSO4(aq) at T=298.15 K" in Journal of Chemical Thermodynamics, 34, no. 11 (2002):1769-1776,
https://doi.org/10.1016/S0021-9614(02)00164-7 . .

TY  - JOUR
AU  - Ninković, Rozalija
AU  - Todorović, M.
AU  - Miladinović, Jelena
PY  - 2001
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/389
AB  - The object of this work was to determine Pitzer's ionic parameters, θ and Ψ, for the mixed salt solution H2O-NaCl-MgCl2 at following temperatures: 273.15, 298.15, 356.15 and 378.15 K in ionic strength interval from 7 to 17.5 mol/kg, using Pitzer-Kim's ionic method. The Pitzer's ionic interaction parameters at all temperatures were evaluated on the bases of solubility data for the system H2O-NaCl-MgCl2, and criterion of diffusion equilibrium. The mean ionic activity coefficient of the NaCl in heterogeneous system, in which NaCl(c) was in equilibrium with saturated mixed solution H2O-NaCl-MgCl2, was obtained using solubility data and criterion of diffusion equilibrium. Temperature dependence of the obtained Pitzer's ionic interaction parameters θ and Ψ,in temperature range from 273.15 to 378.15 K, were described by the polynom of the forth and second order, respectively.
PB  - University of Belgrade, Technical Faculty, Bor
T2  - Journal of Mining and Metallurgy B: Metallurgy
T1  - Solubility and Pitzer's ionic parameters in the system H2O-NaCl-MgCl2
EP  - 65
IS  - 3-4
SP  - 57
VL  - 37
UR  - https://hdl.handle.net/21.15107/rcub_technorep_389
ER  - 

@article{
author = "Ninković, Rozalija and Todorović, M. and Miladinović, Jelena",
year = "2001",
abstract = "The object of this work was to determine Pitzer's ionic parameters, θ and Ψ, for the mixed salt solution H2O-NaCl-MgCl2 at following temperatures: 273.15, 298.15, 356.15 and 378.15 K in ionic strength interval from 7 to 17.5 mol/kg, using Pitzer-Kim's ionic method. The Pitzer's ionic interaction parameters at all temperatures were evaluated on the bases of solubility data for the system H2O-NaCl-MgCl2, and criterion of diffusion equilibrium. The mean ionic activity coefficient of the NaCl in heterogeneous system, in which NaCl(c) was in equilibrium with saturated mixed solution H2O-NaCl-MgCl2, was obtained using solubility data and criterion of diffusion equilibrium. Temperature dependence of the obtained Pitzer's ionic interaction parameters θ and Ψ,in temperature range from 273.15 to 378.15 K, were described by the polynom of the forth and second order, respectively.",
publisher = "University of Belgrade, Technical Faculty, Bor",
journal = "Journal of Mining and Metallurgy B: Metallurgy",
title = "Solubility and Pitzer's ionic parameters in the system H2O-NaCl-MgCl2",
pages = "65-57",
number = "3-4",
volume = "37",
url = "https://hdl.handle.net/21.15107/rcub_technorep_389"
}

Ninković, R., Todorović, M.,& Miladinović, J.. (2001). Solubility and Pitzer's ionic parameters in the system H2O-NaCl-MgCl2. in Journal of Mining and Metallurgy B: Metallurgy
University of Belgrade, Technical Faculty, Bor., 37(3-4), 57-65.
https://hdl.handle.net/21.15107/rcub_technorep_389

Ninković R, Todorović M, Miladinović J. Solubility and Pitzer's ionic parameters in the system H2O-NaCl-MgCl2. in Journal of Mining and Metallurgy B: Metallurgy. 2001;37(3-4):57-65.
https://hdl.handle.net/21.15107/rcub_technorep_389 .

Ninković, Rozalija, Todorović, M., Miladinović, Jelena, "Solubility and Pitzer's ionic parameters in the system H2O-NaCl-MgCl2" in Journal of Mining and Metallurgy B: Metallurgy, 37, no. 3-4 (2001):57-65,
https://hdl.handle.net/21.15107/rcub_technorep_389 .

TY  - JOUR
AU  - Pavićević, Vladimir
AU  - Ninković, Rozalija
AU  - Todorović, M.
AU  - Miladinović, Jelena
PY  - 1999
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/258
AB  - The osmotic coefficients of the mixed electrolyte solution {yNaH(2)PO(4) + (1 - y)Na2SO4}(aq) have been measured by the isopiestic method, at the temperature T = 298.15 K. The activity coefficients of NaH2PO4 and Na2SO4 were calculated by Scatchard's neutral-electrolyte method and by Pitzer and Kim's treatment for mixed-electrolyte solutions. The Scatchard interaction parameters are used for calculation of the excess Gibbs energy as a function of ionic strength and ionic-strength fraction of NaH2PO4. Also, the Zdanovskii's rule of linearity is tested.
PB  - Elsevier Science Bv, Amsterdam
T2  - Fluid Phase Equilibria
T1  - Osmotic and activity coefficients of {yNaH(2)PO(4)+(1-y)Na2SO4}(aq) at the temperature 298.15 K
EP  - 284
IS  - 2
SP  - 275
VL  - 164
DO  - 10.1016/S0378-3812(99)00256-3
ER  - 

@article{
author = "Pavićević, Vladimir and Ninković, Rozalija and Todorović, M. and Miladinović, Jelena",
year = "1999",
abstract = "The osmotic coefficients of the mixed electrolyte solution {yNaH(2)PO(4) + (1 - y)Na2SO4}(aq) have been measured by the isopiestic method, at the temperature T = 298.15 K. The activity coefficients of NaH2PO4 and Na2SO4 were calculated by Scatchard's neutral-electrolyte method and by Pitzer and Kim's treatment for mixed-electrolyte solutions. The Scatchard interaction parameters are used for calculation of the excess Gibbs energy as a function of ionic strength and ionic-strength fraction of NaH2PO4. Also, the Zdanovskii's rule of linearity is tested.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Fluid Phase Equilibria",
title = "Osmotic and activity coefficients of {yNaH(2)PO(4)+(1-y)Na2SO4}(aq) at the temperature 298.15 K",
pages = "284-275",
number = "2",
volume = "164",
doi = "10.1016/S0378-3812(99)00256-3"
}

Pavićević, V., Ninković, R., Todorović, M.,& Miladinović, J.. (1999). Osmotic and activity coefficients of {yNaH(2)PO(4)+(1-y)Na2SO4}(aq) at the temperature 298.15 K. in Fluid Phase Equilibria
Elsevier Science Bv, Amsterdam., 164(2), 275-284.
https://doi.org/10.1016/S0378-3812(99)00256-3

Pavićević V, Ninković R, Todorović M, Miladinović J. Osmotic and activity coefficients of {yNaH(2)PO(4)+(1-y)Na2SO4}(aq) at the temperature 298.15 K. in Fluid Phase Equilibria. 1999;164(2):275-284.
doi:10.1016/S0378-3812(99)00256-3 .

Pavićević, Vladimir, Ninković, Rozalija, Todorović, M., Miladinović, Jelena, "Osmotic and activity coefficients of {yNaH(2)PO(4)+(1-y)Na2SO4}(aq) at the temperature 298.15 K" in Fluid Phase Equilibria, 164, no. 2 (1999):275-284,
https://doi.org/10.1016/S0378-3812(99)00256-3 . .

TY  - JOUR
AU  - Onjia, Antonije
AU  - Milonjić, Slobodan K.
AU  - Todorović, M.
AU  - Loos-Nesković, C
AU  - Fedoroff, A
AU  - Jones, DJ
PY  - 1998
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/178
AB  - Adsorption of various organics on Ni- and Cu-hexacyanoferrates was investigated by gas-solid chromatography (inverse gas chromatography). Adsorption was studied in the temperature region from 80 to 95 degrees C at zero surface coverage. Thermodynamic data of adsorption (standard free energy change, standard state enthalpies, and the entropy changes) were calculated using the surface partition coefficients. Thermodynamic parameters are discussed in terms of surface properties of used adsorbents and physicochemical properties of organic compounds.
PB  - Trans Tech Publications Ltd, Durnten-Zurich
T2  - Materials Science Forum
T1  - Adsorption thermodynamics of organics on nickel- and copper-hexacyanoferrates
EP  - 188
SP  - 183
VL  - 282-2
DO  - 10.4028/www.scientific.net/MSF.282-283.183
ER  - 

@article{
author = "Onjia, Antonije and Milonjić, Slobodan K. and Todorović, M. and Loos-Nesković, C and Fedoroff, A and Jones, DJ",
year = "1998",
abstract = "Adsorption of various organics on Ni- and Cu-hexacyanoferrates was investigated by gas-solid chromatography (inverse gas chromatography). Adsorption was studied in the temperature region from 80 to 95 degrees C at zero surface coverage. Thermodynamic data of adsorption (standard free energy change, standard state enthalpies, and the entropy changes) were calculated using the surface partition coefficients. Thermodynamic parameters are discussed in terms of surface properties of used adsorbents and physicochemical properties of organic compounds.",
publisher = "Trans Tech Publications Ltd, Durnten-Zurich",
journal = "Materials Science Forum",
title = "Adsorption thermodynamics of organics on nickel- and copper-hexacyanoferrates",
pages = "188-183",
volume = "282-2",
doi = "10.4028/www.scientific.net/MSF.282-283.183"
}

Onjia, A., Milonjić, S. K., Todorović, M., Loos-Nesković, C., Fedoroff, A.,& Jones, D.. (1998). Adsorption thermodynamics of organics on nickel- and copper-hexacyanoferrates. in Materials Science Forum
Trans Tech Publications Ltd, Durnten-Zurich., 282-2, 183-188.
https://doi.org/10.4028/www.scientific.net/MSF.282-283.183

Onjia A, Milonjić SK, Todorović M, Loos-Nesković C, Fedoroff A, Jones D. Adsorption thermodynamics of organics on nickel- and copper-hexacyanoferrates. in Materials Science Forum. 1998;282-2:183-188.
doi:10.4028/www.scientific.net/MSF.282-283.183 .

Onjia, Antonije, Milonjić, Slobodan K., Todorović, M., Loos-Nesković, C, Fedoroff, A, Jones, DJ, "Adsorption thermodynamics of organics on nickel- and copper-hexacyanoferrates" in Materials Science Forum, 282-2 (1998):183-188,
https://doi.org/10.4028/www.scientific.net/MSF.282-283.183 . .

TY  - JOUR
AU  - Todorović, M.
AU  - Ninković, Rozalija
AU  - Miladinović, Jelena
PY  - 1998
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/215
AB  - 'The osmotic coefficients of the mixed electrolyte solution {yK(2)SO(4) + (1 - y)Mg(NO3)(2)}(aq) have been measured by the isopiestic method, at the temperature T = 298.15 K. The activity coefficients of K2SO4 and Mg(NO3)(2) were calculated by Scatchard's neutral-electrolyte method and by Fitter and Kim's treatment for mixed electrolyte solutions. The results are used for calculation of the excess Gibbs energy as a function of ionic strength and ionic-strength fraction of K2SO4, and also as a test of Zdanovskii's rule of linearity.
PB  - Academic Press Ltd, London
T2  - Journal of Chemical Thermodynamics
T1  - Osmotic and activity coefficients of {yK(2)SO(4)+(1-y)Mg(NO3)(2)}(aq) at the temperature T = 298.15 K
EP  - 853
IS  - 7
SP  - 847
VL  - 30
DO  - 10.1006/jcht.1998.0351
ER  - 

@article{
author = "Todorović, M. and Ninković, Rozalija and Miladinović, Jelena",
year = "1998",
abstract = "'The osmotic coefficients of the mixed electrolyte solution {yK(2)SO(4) + (1 - y)Mg(NO3)(2)}(aq) have been measured by the isopiestic method, at the temperature T = 298.15 K. The activity coefficients of K2SO4 and Mg(NO3)(2) were calculated by Scatchard's neutral-electrolyte method and by Fitter and Kim's treatment for mixed electrolyte solutions. The results are used for calculation of the excess Gibbs energy as a function of ionic strength and ionic-strength fraction of K2SO4, and also as a test of Zdanovskii's rule of linearity.",
publisher = "Academic Press Ltd, London",
journal = "Journal of Chemical Thermodynamics",
title = "Osmotic and activity coefficients of {yK(2)SO(4)+(1-y)Mg(NO3)(2)}(aq) at the temperature T = 298.15 K",
pages = "853-847",
number = "7",
volume = "30",
doi = "10.1006/jcht.1998.0351"
}

Todorović, M., Ninković, R.,& Miladinović, J.. (1998). Osmotic and activity coefficients of {yK(2)SO(4)+(1-y)Mg(NO3)(2)}(aq) at the temperature T = 298.15 K. in Journal of Chemical Thermodynamics
Academic Press Ltd, London., 30(7), 847-853.
https://doi.org/10.1006/jcht.1998.0351

Todorović M, Ninković R, Miladinović J. Osmotic and activity coefficients of {yK(2)SO(4)+(1-y)Mg(NO3)(2)}(aq) at the temperature T = 298.15 K. in Journal of Chemical Thermodynamics. 1998;30(7):847-853.
doi:10.1006/jcht.1998.0351 .

Todorović, M., Ninković, Rozalija, Miladinović, Jelena, "Osmotic and activity coefficients of {yK(2)SO(4)+(1-y)Mg(NO3)(2)}(aq) at the temperature T = 298.15 K" in Journal of Chemical Thermodynamics, 30, no. 7 (1998):847-853,
https://doi.org/10.1006/jcht.1998.0351 . .