TY  - JOUR
AU  - Marić, Aleksandar
AU  - Jovanov, Pavle
AU  - Gadžurić, Slobodan
AU  - Trtić-Petrović, Tatjana
AU  - Sakač, Marijana
AU  - Tot, Aleksandar
AU  - Bertić, Marko
AU  - Vraneš, Milan
PY  - 2023
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/12042
AB  - 5-Hydroxymethylfurfural (HMF), a Maillard reaction product, can be formed when honey is subjected to heat treatment or a long storage time, becoming volatile and toxic depending on its concentration. The fact that, until today, there is no literature data on the extraction of 5-hydroxymethylfurfural (HMF) from honey using ionic liquids directed the investigation of the influence of biodegradable cholinium ionic liquids on the formation of aqueous biphasic systems and the application of these systems for the extraction of HMF from honey. The influence of anions of synthesised ionic liquids on the construction of biphasic systems in which an inorganic salt was used as a salting agent was investigated. Then, the extraction of HMF in these systems was examined, and the mechanisms of HMF extraction using ionic liquids were explained using computer simulations. Examining the effect of cholinium ionic liquids (choline chloride ([Ch][Cl]), cholinium nicotinate ([Ch][Nic]), cholinium propionate ([Ch][Prop]), and cholinium butyrate ([Ch][But])) on the formation of aqueous biphasic systems by comparing the phase diagrams, it was concluded that the ability of ionic liquids to form an aqueous biphasic system with tripotassium phosphate (K3PO4) decreases in the following order: [Ch][But] z [Ch][Prop] > [Ch][Nic] > [Ch][Cl]. By applying all tested aqueous biphasic systems for the extraction of HMF from honey, an extraction efficiency of more than 89% was achieved. Complete extraction was achieved using the extraction system with [Ch][But], while the weakest ability to extract HMF was exhibited by the system with [Ch][Cl]. The mechanisms of HMF extraction using ionic liquids are explained on the basis of the optimised structures of the ionic liquid systems with HMF, together with the visualisation of noncovalent interactions, and on the basis of the calculated binding energies DGbin, which can be used as a good predictor of the extraction potential of newly synthesised ionic liquids
T2  - RSC Advances
T1  - Application of biodegradable cholinium ionic liquids for the extraction of 5-hydroxymethylfurfural (HMF) from honey
VL  - 13
IS  - 46
SP  - 32714
EP  - 32721
DO  - 10.1039/D3RA06077B
ER  - 

@article{
author = "Marić, Aleksandar and Jovanov, Pavle and Gadžurić, Slobodan and Trtić-Petrović, Tatjana and Sakač, Marijana and Tot, Aleksandar and Bertić, Marko and Vraneš, Milan",
year = "2023",
abstract = "5-Hydroxymethylfurfural (HMF), a Maillard reaction product, can be formed when honey is subjected to heat treatment or a long storage time, becoming volatile and toxic depending on its concentration. The fact that, until today, there is no literature data on the extraction of 5-hydroxymethylfurfural (HMF) from honey using ionic liquids directed the investigation of the influence of biodegradable cholinium ionic liquids on the formation of aqueous biphasic systems and the application of these systems for the extraction of HMF from honey. The influence of anions of synthesised ionic liquids on the construction of biphasic systems in which an inorganic salt was used as a salting agent was investigated. Then, the extraction of HMF in these systems was examined, and the mechanisms of HMF extraction using ionic liquids were explained using computer simulations. Examining the effect of cholinium ionic liquids (choline chloride ([Ch][Cl]), cholinium nicotinate ([Ch][Nic]), cholinium propionate ([Ch][Prop]), and cholinium butyrate ([Ch][But])) on the formation of aqueous biphasic systems by comparing the phase diagrams, it was concluded that the ability of ionic liquids to form an aqueous biphasic system with tripotassium phosphate (K3PO4) decreases in the following order: [Ch][But] z [Ch][Prop] > [Ch][Nic] > [Ch][Cl]. By applying all tested aqueous biphasic systems for the extraction of HMF from honey, an extraction efficiency of more than 89% was achieved. Complete extraction was achieved using the extraction system with [Ch][But], while the weakest ability to extract HMF was exhibited by the system with [Ch][Cl]. The mechanisms of HMF extraction using ionic liquids are explained on the basis of the optimised structures of the ionic liquid systems with HMF, together with the visualisation of noncovalent interactions, and on the basis of the calculated binding energies DGbin, which can be used as a good predictor of the extraction potential of newly synthesised ionic liquids",
journal = "RSC Advances",
title = "Application of biodegradable cholinium ionic liquids for the extraction of 5-hydroxymethylfurfural (HMF) from honey",
volume = "13",
number = "46",
pages = "32714-32721",
doi = "10.1039/D3RA06077B"
}

Marić, A., Jovanov, P., Gadžurić, S., Trtić-Petrović, T., Sakač, M., Tot, A., Bertić, M.,& Vraneš, M.. (2023). Application of biodegradable cholinium ionic liquids for the extraction of 5-hydroxymethylfurfural (HMF) from honey. in RSC Advances, 13(46), 32714-32721.
https://doi.org/10.1039/D3RA06077B

Marić A, Jovanov P, Gadžurić S, Trtić-Petrović T, Sakač M, Tot A, Bertić M, Vraneš M. Application of biodegradable cholinium ionic liquids for the extraction of 5-hydroxymethylfurfural (HMF) from honey. in RSC Advances. 2023;13(46):32714-32721.
doi:10.1039/D3RA06077B .

Marić, Aleksandar, Jovanov, Pavle, Gadžurić, Slobodan, Trtić-Petrović, Tatjana, Sakač, Marijana, Tot, Aleksandar, Bertić, Marko, Vraneš, Milan, "Application of biodegradable cholinium ionic liquids for the extraction of 5-hydroxymethylfurfural (HMF) from honey" in RSC Advances, 13, no. 46 (2023):32714-32721,
https://doi.org/10.1039/D3RA06077B . .

TY  - JOUR
AU  - Ražić, Slavica
AU  - Gadžurić, Slobodan
AU  - Trtić-Petrović, Tatjana
PY  - 2023
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/12045
AB  - The widespread use of ionic liquids (ILs) as greener solvents in analytical sciences, especially in sample pretreatment, has focused attention on exploiting their enormous potential, not only on eliminating and improving the drawbacks faced by scientists. These ionic compounds with unique physicochemical properties can be tuned through smart synthesis, combining cations and anions, so that the compound exhibits excellent properties for its intended purpose. Ionic liquids are rightly referred to as designer solvents. Validation of a newly proposed analytical methods using ionic liquids, either in sample preparation or in further analysis, is a critical process to demonstrate that a particular analytical method is fit for purpose and provides reliable and accurate results. In addition, this article specially addressed the potential toxicity of ionic liquids with the modest goal of assisting researchers in this field by expanding their target areas.
T2  - Analytical and Bioanalytical Chemistry
T1  - Ionic liquids in green analytical chemistry—are they that good and green enough?
DO  - 10.1007/s00216-023-05045-3
ER  - 

@article{
author = "Ražić, Slavica and Gadžurić, Slobodan and Trtić-Petrović, Tatjana",
year = "2023",
abstract = "The widespread use of ionic liquids (ILs) as greener solvents in analytical sciences, especially in sample pretreatment, has focused attention on exploiting their enormous potential, not only on eliminating and improving the drawbacks faced by scientists. These ionic compounds with unique physicochemical properties can be tuned through smart synthesis, combining cations and anions, so that the compound exhibits excellent properties for its intended purpose. Ionic liquids are rightly referred to as designer solvents. Validation of a newly proposed analytical methods using ionic liquids, either in sample preparation or in further analysis, is a critical process to demonstrate that a particular analytical method is fit for purpose and provides reliable and accurate results. In addition, this article specially addressed the potential toxicity of ionic liquids with the modest goal of assisting researchers in this field by expanding their target areas.",
journal = "Analytical and Bioanalytical Chemistry",
title = "Ionic liquids in green analytical chemistry—are they that good and green enough?",
doi = "10.1007/s00216-023-05045-3"
}

Ražić, S., Gadžurić, S.,& Trtić-Petrović, T.. (2023). Ionic liquids in green analytical chemistry—are they that good and green enough?. in Analytical and Bioanalytical Chemistry.
https://doi.org/10.1007/s00216-023-05045-3

Ražić S, Gadžurić S, Trtić-Petrović T. Ionic liquids in green analytical chemistry—are they that good and green enough?. in Analytical and Bioanalytical Chemistry. 2023;.
doi:10.1007/s00216-023-05045-3 .

Ražić, Slavica, Gadžurić, Slobodan, Trtić-Petrović, Tatjana, "Ionic liquids in green analytical chemistry—are they that good and green enough?" in Analytical and Bioanalytical Chemistry (2023),
https://doi.org/10.1007/s00216-023-05045-3 . .

TY  - JOUR
AU  - Lazarević, Dajana
AU  - Mušović, Jasmina
AU  - Trtić-Petrović, Tatjana M.
AU  - Gadžurić, Slobodan
PY  - 2023
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/10772
AB  - In this work, aqueous biphasic systems (ABSs) formed by copolymers, ionic liquids (ILs) and natural deep eutectic solvents (NADES) have been demonstrated to be effective separation platforms for the extraction of hydrophobic pharmaceutical ingredients such as parthenolide (PAR). This work addresses the determination of the liquid–liquid equilibrium of ABS composed of choline lactate IL or choline chloride – lactic acid NADES and two different block copolymers Pluronic (PL17R4 and PL10R5), and their influence on the ABS formation and extraction efficiency of PAR. The ability of Pluronics to form ABS is compared to widely used polypropylene glycol polymer (PPG400). Comparing the effect of the ionic liquid and NADES on the ABS formation, it is shown that both salting-our reagents successfully form ABS and do not affect the extraction efficiency of PAR. The main influence on the high parthenolide extraction efficiency (>96%) is governed by the hydrophobic interactions between Pluronic and investigated compound, regardless on the applied salting-out reagent. Due to a high extraction efficiency achieved in PL-rich phase and promissing medical features of PAR, obtained results showed that this phase could be used as biocompatible drug delivery system. Avoiding commercially available organic solvents, elevated temperatures and pressure, the proposed method is greener alternative for PAR extraction.
T2  - Separation and Purification Technology
T1  - Partition of parthenolide in ternary {block copolymer + biocompatible ionic liquid or natural deep eutectic solvent + water} systems
VL  - 314
SP  - 123653
DO  - 10.1016/j.seppur.2023.123653
ER  - 

@article{
author = "Lazarević, Dajana and Mušović, Jasmina and Trtić-Petrović, Tatjana M. and Gadžurić, Slobodan",
year = "2023",
abstract = "In this work, aqueous biphasic systems (ABSs) formed by copolymers, ionic liquids (ILs) and natural deep eutectic solvents (NADES) have been demonstrated to be effective separation platforms for the extraction of hydrophobic pharmaceutical ingredients such as parthenolide (PAR). This work addresses the determination of the liquid–liquid equilibrium of ABS composed of choline lactate IL or choline chloride – lactic acid NADES and two different block copolymers Pluronic (PL17R4 and PL10R5), and their influence on the ABS formation and extraction efficiency of PAR. The ability of Pluronics to form ABS is compared to widely used polypropylene glycol polymer (PPG400). Comparing the effect of the ionic liquid and NADES on the ABS formation, it is shown that both salting-our reagents successfully form ABS and do not affect the extraction efficiency of PAR. The main influence on the high parthenolide extraction efficiency (>96%) is governed by the hydrophobic interactions between Pluronic and investigated compound, regardless on the applied salting-out reagent. Due to a high extraction efficiency achieved in PL-rich phase and promissing medical features of PAR, obtained results showed that this phase could be used as biocompatible drug delivery system. Avoiding commercially available organic solvents, elevated temperatures and pressure, the proposed method is greener alternative for PAR extraction.",
journal = "Separation and Purification Technology",
title = "Partition of parthenolide in ternary {block copolymer + biocompatible ionic liquid or natural deep eutectic solvent + water} systems",
volume = "314",
pages = "123653",
doi = "10.1016/j.seppur.2023.123653"
}

Lazarević, D., Mušović, J., Trtić-Petrović, T. M.,& Gadžurić, S.. (2023). Partition of parthenolide in ternary {block copolymer + biocompatible ionic liquid or natural deep eutectic solvent + water} systems. in Separation and Purification Technology, 314, 123653.
https://doi.org/10.1016/j.seppur.2023.123653

Lazarević D, Mušović J, Trtić-Petrović TM, Gadžurić S. Partition of parthenolide in ternary {block copolymer + biocompatible ionic liquid or natural deep eutectic solvent + water} systems. in Separation and Purification Technology. 2023;314:123653.
doi:10.1016/j.seppur.2023.123653 .

Lazarević, Dajana, Mušović, Jasmina, Trtić-Petrović, Tatjana M., Gadžurić, Slobodan, "Partition of parthenolide in ternary {block copolymer + biocompatible ionic liquid or natural deep eutectic solvent + water} systems" in Separation and Purification Technology, 314 (2023):123653,
https://doi.org/10.1016/j.seppur.2023.123653 . .

TY  - JOUR
AU  - Mušović, Jasmina
AU  - Vraneš, Milan
AU  - Papović, Snežana
AU  - Gadžurić, Slobodan
AU  - Ražić, Slavica
AU  - Trtić-Petrović, Tatjana M.
PY  - 2023
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/10596
AB  - Although sample preparation, as an unavoidable step of the analytical process should be simple, it is very often identified as a bottleneck. Simplicity of sample preparation based on cost-effective and non-hazardous materials is mandatory for any sustainable and environmental friendly approach. Aqueous biphasic systems (ABS), based on functionalized ionic liquids (FILs) are acceptable alternatives to classical extraction procedures, due to the replacement of organic solvent with diluted aqueous-soluble ionic liquids. In this work, two water soluble FILs based on 2-mercaptobenzothiazolate anion, [mbt]: 1-butyl-3-methylimidazolium [mbt] ([bmim][mbt]) and 1-ethyl-3-methylimidazolium [mbt] ([emim][mbt]), were designed and synthesized in order to selectively extract Cd(II) and Pb(II) from the river sediment. It was found that [mbt]– anion acts as the ligand and forms complexes with Cd(II) and Pb(II) which are responsible for their efficient extraction, while cation is more responsible for the formation of ABS. Partition coefficients of 408 and 180 for Cd(II) and Pb(II), respectively, were obtained using ABS based on [bmim][mbt]. Direct extraction of Cd(II) and Pb(II) from the river sediment has been investigated and obtained optimal conditions are: 60 min direct contact of the aqueous solution of [bmim][mbt] and the sediment sample at 90 °C, followed by formation of ABS upon addition of potassium citrate. Using AGRE and AGREEprep tools greenness of the proposed method for direct extraction of Cd(II) and Pb(II) from the sediment are calculated. Obtained values of 0.69 and 0.71 for Cd(II) and Pb(II) extraction, respectively, showed a high level of the greenness of the proposed method.
T2  - Journal of Molecular Liquids
T1  - Greener sample preparation method for direct determination of Cd(II) and Pb(II) in river sediment based on an aqueous biphasic system with functionalized ionic liquids
VL  - 369
SP  - 120974
DO  - 10.1016/j.molliq.2022.120974
ER  - 

@article{
author = "Mušović, Jasmina and Vraneš, Milan and Papović, Snežana and Gadžurić, Slobodan and Ražić, Slavica and Trtić-Petrović, Tatjana M.",
year = "2023",
abstract = "Although sample preparation, as an unavoidable step of the analytical process should be simple, it is very often identified as a bottleneck. Simplicity of sample preparation based on cost-effective and non-hazardous materials is mandatory for any sustainable and environmental friendly approach. Aqueous biphasic systems (ABS), based on functionalized ionic liquids (FILs) are acceptable alternatives to classical extraction procedures, due to the replacement of organic solvent with diluted aqueous-soluble ionic liquids. In this work, two water soluble FILs based on 2-mercaptobenzothiazolate anion, [mbt]: 1-butyl-3-methylimidazolium [mbt] ([bmim][mbt]) and 1-ethyl-3-methylimidazolium [mbt] ([emim][mbt]), were designed and synthesized in order to selectively extract Cd(II) and Pb(II) from the river sediment. It was found that [mbt]– anion acts as the ligand and forms complexes with Cd(II) and Pb(II) which are responsible for their efficient extraction, while cation is more responsible for the formation of ABS. Partition coefficients of 408 and 180 for Cd(II) and Pb(II), respectively, were obtained using ABS based on [bmim][mbt]. Direct extraction of Cd(II) and Pb(II) from the river sediment has been investigated and obtained optimal conditions are: 60 min direct contact of the aqueous solution of [bmim][mbt] and the sediment sample at 90 °C, followed by formation of ABS upon addition of potassium citrate. Using AGRE and AGREEprep tools greenness of the proposed method for direct extraction of Cd(II) and Pb(II) from the sediment are calculated. Obtained values of 0.69 and 0.71 for Cd(II) and Pb(II) extraction, respectively, showed a high level of the greenness of the proposed method.",
journal = "Journal of Molecular Liquids",
title = "Greener sample preparation method for direct determination of Cd(II) and Pb(II) in river sediment based on an aqueous biphasic system with functionalized ionic liquids",
volume = "369",
pages = "120974",
doi = "10.1016/j.molliq.2022.120974"
}

Mušović, J., Vraneš, M., Papović, S., Gadžurić, S., Ražić, S.,& Trtić-Petrović, T. M.. (2023). Greener sample preparation method for direct determination of Cd(II) and Pb(II) in river sediment based on an aqueous biphasic system with functionalized ionic liquids. in Journal of Molecular Liquids, 369, 120974.
https://doi.org/10.1016/j.molliq.2022.120974

Mušović J, Vraneš M, Papović S, Gadžurić S, Ražić S, Trtić-Petrović TM. Greener sample preparation method for direct determination of Cd(II) and Pb(II) in river sediment based on an aqueous biphasic system with functionalized ionic liquids. in Journal of Molecular Liquids. 2023;369:120974.
doi:10.1016/j.molliq.2022.120974 .

Mušović, Jasmina, Vraneš, Milan, Papović, Snežana, Gadžurić, Slobodan, Ražić, Slavica, Trtić-Petrović, Tatjana M., "Greener sample preparation method for direct determination of Cd(II) and Pb(II) in river sediment based on an aqueous biphasic system with functionalized ionic liquids" in Journal of Molecular Liquids, 369 (2023):120974,
https://doi.org/10.1016/j.molliq.2022.120974 . .

TY  - JOUR
AU  - Jelić, Dijana
AU  - Papović, Snežana
AU  - Vraneš, Milan
AU  - Gadžurić, Slobodan
AU  - Berto, Silvia
AU  - Alladio, Eugenio
AU  - Gajić, Dragana
AU  - Janković, Bojan Ž.
PY  - 2021
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/10048
AB  - Ambroxol hydrochloride (AMB), used as a broncho secretolytic and an expectorant drug, is a semi-synthetic derivative of vasicine obtained from the Indian shrub Adhatoda vasica. It is a metabolic product of bromhexine. The paper provides comprehensive and detailed research on ambroxol hydrochloride, gives information on thermal stability, the mechanism of AMB degradation, and data of practical interest for optimization of formulation that contains AMB as an active compound. Investigation on pure AMB and in commercial formulation Flavamed® tablet (FT), which contains AMB as an active compound, was performed systematically using thermal and spectroscopic methods, along with a sophisticated and practical statistical approach. AMB proved to be a heat-stable and humidity-sensitive drug. For its successful formulation, special attention should be addressed to excipients since it was found that polyvinyl pyrrolidone and Mg stearate affect the thermal stability of AMB. At the same time, lactose monohydrate contributes to faster degradation of AMB and change in decomposition mechanism. It was found that the n-th order kinetic model mechanistically best describes the decomposition process of pure AMB and in Flavamed® tablets.
T2  - Pharmaceutics
T1  - Thermo-Analytical and Compatibility Study with Mechanistic Explanation of Degradation Kinetics of Ambroxol Hydrochloride Tablets under Non-Isothermal Conditions
VL  - 13
IS  - 11
SP  - 1910
DO  - 10.3390/pharmaceutics13111910
ER  - 

@article{
author = "Jelić, Dijana and Papović, Snežana and Vraneš, Milan and Gadžurić, Slobodan and Berto, Silvia and Alladio, Eugenio and Gajić, Dragana and Janković, Bojan Ž.",
year = "2021",
abstract = "Ambroxol hydrochloride (AMB), used as a broncho secretolytic and an expectorant drug, is a semi-synthetic derivative of vasicine obtained from the Indian shrub Adhatoda vasica. It is a metabolic product of bromhexine. The paper provides comprehensive and detailed research on ambroxol hydrochloride, gives information on thermal stability, the mechanism of AMB degradation, and data of practical interest for optimization of formulation that contains AMB as an active compound. Investigation on pure AMB and in commercial formulation Flavamed® tablet (FT), which contains AMB as an active compound, was performed systematically using thermal and spectroscopic methods, along with a sophisticated and practical statistical approach. AMB proved to be a heat-stable and humidity-sensitive drug. For its successful formulation, special attention should be addressed to excipients since it was found that polyvinyl pyrrolidone and Mg stearate affect the thermal stability of AMB. At the same time, lactose monohydrate contributes to faster degradation of AMB and change in decomposition mechanism. It was found that the n-th order kinetic model mechanistically best describes the decomposition process of pure AMB and in Flavamed® tablets.",
journal = "Pharmaceutics",
title = "Thermo-Analytical and Compatibility Study with Mechanistic Explanation of Degradation Kinetics of Ambroxol Hydrochloride Tablets under Non-Isothermal Conditions",
volume = "13",
number = "11",
pages = "1910",
doi = "10.3390/pharmaceutics13111910"
}

Jelić, D., Papović, S., Vraneš, M., Gadžurić, S., Berto, S., Alladio, E., Gajić, D.,& Janković, B. Ž.. (2021). Thermo-Analytical and Compatibility Study with Mechanistic Explanation of Degradation Kinetics of Ambroxol Hydrochloride Tablets under Non-Isothermal Conditions. in Pharmaceutics, 13(11), 1910.
https://doi.org/10.3390/pharmaceutics13111910

Jelić D, Papović S, Vraneš M, Gadžurić S, Berto S, Alladio E, Gajić D, Janković BŽ. Thermo-Analytical and Compatibility Study with Mechanistic Explanation of Degradation Kinetics of Ambroxol Hydrochloride Tablets under Non-Isothermal Conditions. in Pharmaceutics. 2021;13(11):1910.
doi:10.3390/pharmaceutics13111910 .

Jelić, Dijana, Papović, Snežana, Vraneš, Milan, Gadžurić, Slobodan, Berto, Silvia, Alladio, Eugenio, Gajić, Dragana, Janković, Bojan Ž., "Thermo-Analytical and Compatibility Study with Mechanistic Explanation of Degradation Kinetics of Ambroxol Hydrochloride Tablets under Non-Isothermal Conditions" in Pharmaceutics, 13, no. 11 (2021):1910,
https://doi.org/10.3390/pharmaceutics13111910 . .

TY  - JOUR
AU  - Jocić, Ana
AU  - Marić, Slađana
AU  - Dimitrijević, Aleksandra
AU  - Tot, Aleksandar
AU  - Gadžurić, Slobodan
AU  - Vraneš, Milan
AU  - Trtić-Petrović, Tatjana M.
PY  - 2020
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8835
AB  - This work addresses use of a set of 2-hydroxypropylammonium based protic ionic liquids (PILs) as adjuvants in the aqueous biphasic system (ABS) composed of polyethylene glycol, with molecular weight 2000 g/mol (PEG 2000) and potassium carbonate. The phase diagrams were determined at 25 °C for ABS without and with the addition of 5 wt% of PIL. Comparative analysis of solubility curves indicates that PILs influence liquid-liquid equilibria of PEG 2000-K2CO3 ABS by heightening the hydrophilicity of a PEG-rich phase in various degrees. The compositions of the phases (tie lines) were determined for the selected ABS mixture composition, 26 wt% of PEG 2000 + 10 wt% of K2CO3, without and with 5 wt% of PILs, that is further used for the separation studies. The distribution of PILs between two phases is mainly dependent on specific PEG-PIL interactions and on the PIL content in ABS mixture. The experimental results are supported by molecular simulations that contributed to a broader picture of underlying effects of PILs as adjuvants on ABS formation. The partition of four dye compounds, Remazol Brilliant Blue R (RBBR), Orange II (OII), Rhodamine B (RB) and Congo Red (CR), as probe molecules with different intrinsic properties, was investigated. Obtained results show that the addition of PILs can improve the extraction of hydrophilic and charged compounds as OII, RBBR and CR in PEG-rich phase. On the other hand, it promotes the extraction of hydrophobic and neutral solutes as RB in salt-rich phase. By the addition of the most hydrophilic 3-chloropropanoate based PIL in the PEG 2000-K2CO3 ABS 12 times higher separation factor for OII and RB was achieved. © 2020 Elsevier B.V.
T2  - Journal of Molecular Liquids
T1  - Protic ionic liquids as adjuvants to enhance extraction and separation performance of diverse polarity compounds in PEG-salt based aqueous biphasic system
VL  - 303
SP  - 112484
DO  - 10.1016/j.molliq.2020.112484
ER  - 

@article{
author = "Jocić, Ana and Marić, Slađana and Dimitrijević, Aleksandra and Tot, Aleksandar and Gadžurić, Slobodan and Vraneš, Milan and Trtić-Petrović, Tatjana M.",
year = "2020",
abstract = "This work addresses use of a set of 2-hydroxypropylammonium based protic ionic liquids (PILs) as adjuvants in the aqueous biphasic system (ABS) composed of polyethylene glycol, with molecular weight 2000 g/mol (PEG 2000) and potassium carbonate. The phase diagrams were determined at 25 °C for ABS without and with the addition of 5 wt% of PIL. Comparative analysis of solubility curves indicates that PILs influence liquid-liquid equilibria of PEG 2000-K2CO3 ABS by heightening the hydrophilicity of a PEG-rich phase in various degrees. The compositions of the phases (tie lines) were determined for the selected ABS mixture composition, 26 wt% of PEG 2000 + 10 wt% of K2CO3, without and with 5 wt% of PILs, that is further used for the separation studies. The distribution of PILs between two phases is mainly dependent on specific PEG-PIL interactions and on the PIL content in ABS mixture. The experimental results are supported by molecular simulations that contributed to a broader picture of underlying effects of PILs as adjuvants on ABS formation. The partition of four dye compounds, Remazol Brilliant Blue R (RBBR), Orange II (OII), Rhodamine B (RB) and Congo Red (CR), as probe molecules with different intrinsic properties, was investigated. Obtained results show that the addition of PILs can improve the extraction of hydrophilic and charged compounds as OII, RBBR and CR in PEG-rich phase. On the other hand, it promotes the extraction of hydrophobic and neutral solutes as RB in salt-rich phase. By the addition of the most hydrophilic 3-chloropropanoate based PIL in the PEG 2000-K2CO3 ABS 12 times higher separation factor for OII and RB was achieved. © 2020 Elsevier B.V.",
journal = "Journal of Molecular Liquids",
title = "Protic ionic liquids as adjuvants to enhance extraction and separation performance of diverse polarity compounds in PEG-salt based aqueous biphasic system",
volume = "303",
pages = "112484",
doi = "10.1016/j.molliq.2020.112484"
}

Jocić, A., Marić, S., Dimitrijević, A., Tot, A., Gadžurić, S., Vraneš, M.,& Trtić-Petrović, T. M.. (2020). Protic ionic liquids as adjuvants to enhance extraction and separation performance of diverse polarity compounds in PEG-salt based aqueous biphasic system. in Journal of Molecular Liquids, 303, 112484.
https://doi.org/10.1016/j.molliq.2020.112484

Jocić A, Marić S, Dimitrijević A, Tot A, Gadžurić S, Vraneš M, Trtić-Petrović TM. Protic ionic liquids as adjuvants to enhance extraction and separation performance of diverse polarity compounds in PEG-salt based aqueous biphasic system. in Journal of Molecular Liquids. 2020;303:112484.
doi:10.1016/j.molliq.2020.112484 .

Jocić, Ana, Marić, Slađana, Dimitrijević, Aleksandra, Tot, Aleksandar, Gadžurić, Slobodan, Vraneš, Milan, Trtić-Petrović, Tatjana M., "Protic ionic liquids as adjuvants to enhance extraction and separation performance of diverse polarity compounds in PEG-salt based aqueous biphasic system" in Journal of Molecular Liquids, 303 (2020):112484,
https://doi.org/10.1016/j.molliq.2020.112484 . .

TY  - JOUR
AU  - Dimitrijević, Aleksandra
AU  - Мilićević, Jelena
AU  - Jocić, Ana
AU  - Marić, Slađana
AU  - Trtić-Petrović, Tatjana M.
AU  - Papović, Snežana
AU  - Tot, Aleksandar
AU  - Gadžurić, Slobodan
AU  - Vraneš, Milan
PY  - 2020
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8833
AB  - Despite a large collection of publications dealing with the characterization of ionic liquid-based aqueous biphasic systems (IL-ABS), a gap still exists regarding the impact of functionalized alkyl side branches and IL positional isomers on phase equilibria. Therefore, this work addresses the investigation of the ability of different methyl substituted pyridinium based ILs on the formation of ABSs with K3PO4. We evaluated the impact of (i) functional groups (hydroxyl or ether) embed in side alkyl chains of pyridinium cations, (ii) positional isomerism of methyl group (ortho, meta and para) and (iii) the IL cation core. Ternary phase diagrams of the ABSs formed by these ILs and K3PO4 and the appropriate tie lines were determined and presented. It is shown that the presence of functionalized alkyl chain largely affects the salting-in behavior of ILs (ILs with the oxygen groups are more difficult to form ABS) while more subtle differences were observed among positional isomers. Based on the obtained results it is concluded that change of biphasic area of ABS is the manifestation of the altered affinity of ILs for water as a consequence of cation structure. Moreover, aiming at gathering a broader picture of the relationship between ILs structure and ABS properties, molecular simulations were performed, and it was showed that the obtained results are consistent with the experimental results. © 2020 Elsevier B.V.
T2  - Fluid Phase Equilibria
T1  - Further insight into the influence of functionalization and positional isomerism of pyridinium ionic liquids on the aqueous two-phase system equilibria
VL  - 512
SP  - 112520
DO  - 10.1016/j.fluid.2020.112520
ER  - 

@article{
author = "Dimitrijević, Aleksandra and Мilićević, Jelena and Jocić, Ana and Marić, Slađana and Trtić-Petrović, Tatjana M. and Papović, Snežana and Tot, Aleksandar and Gadžurić, Slobodan and Vraneš, Milan",
year = "2020",
abstract = "Despite a large collection of publications dealing with the characterization of ionic liquid-based aqueous biphasic systems (IL-ABS), a gap still exists regarding the impact of functionalized alkyl side branches and IL positional isomers on phase equilibria. Therefore, this work addresses the investigation of the ability of different methyl substituted pyridinium based ILs on the formation of ABSs with K3PO4. We evaluated the impact of (i) functional groups (hydroxyl or ether) embed in side alkyl chains of pyridinium cations, (ii) positional isomerism of methyl group (ortho, meta and para) and (iii) the IL cation core. Ternary phase diagrams of the ABSs formed by these ILs and K3PO4 and the appropriate tie lines were determined and presented. It is shown that the presence of functionalized alkyl chain largely affects the salting-in behavior of ILs (ILs with the oxygen groups are more difficult to form ABS) while more subtle differences were observed among positional isomers. Based on the obtained results it is concluded that change of biphasic area of ABS is the manifestation of the altered affinity of ILs for water as a consequence of cation structure. Moreover, aiming at gathering a broader picture of the relationship between ILs structure and ABS properties, molecular simulations were performed, and it was showed that the obtained results are consistent with the experimental results. © 2020 Elsevier B.V.",
journal = "Fluid Phase Equilibria",
title = "Further insight into the influence of functionalization and positional isomerism of pyridinium ionic liquids on the aqueous two-phase system equilibria",
volume = "512",
pages = "112520",
doi = "10.1016/j.fluid.2020.112520"
}

Dimitrijević, A., Мilićević, J., Jocić, A., Marić, S., Trtić-Petrović, T. M., Papović, S., Tot, A., Gadžurić, S.,& Vraneš, M.. (2020). Further insight into the influence of functionalization and positional isomerism of pyridinium ionic liquids on the aqueous two-phase system equilibria. in Fluid Phase Equilibria, 512, 112520.
https://doi.org/10.1016/j.fluid.2020.112520

Dimitrijević A, Мilićević J, Jocić A, Marić S, Trtić-Petrović TM, Papović S, Tot A, Gadžurić S, Vraneš M. Further insight into the influence of functionalization and positional isomerism of pyridinium ionic liquids on the aqueous two-phase system equilibria. in Fluid Phase Equilibria. 2020;512:112520.
doi:10.1016/j.fluid.2020.112520 .

Dimitrijević, Aleksandra, Мilićević, Jelena, Jocić, Ana, Marić, Slađana, Trtić-Petrović, Tatjana M., Papović, Snežana, Tot, Aleksandar, Gadžurić, Slobodan, Vraneš, Milan, "Further insight into the influence of functionalization and positional isomerism of pyridinium ionic liquids on the aqueous two-phase system equilibria" in Fluid Phase Equilibria, 512 (2020):112520,
https://doi.org/10.1016/j.fluid.2020.112520 . .

TY  - JOUR
AU  - Dimitrijević, Aleksandra
AU  - Tavares, Ana Paula M.
AU  - Almeida, Mafalda R.
AU  - Vraneš, Milan
AU  - Sousa, Ana C. A.
AU  - Cristovão, Ana Clara
AU  - Trtić-Petrović, Tatjana M.
AU  - Gadžurić, Slobodan
AU  - Freire, Mara G.
PY  - 2020
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8974
AB  - Expired energy drinks are rich in bioactive value-added compounds that can be recovered and reused in order to valorize food waste within a circular economy perspective. However, to accomplish such requirements, it is necessary to develop sustainable extraction and recovery processes, which must consist of decreasing the number of steps required or developing integrated strategies. In this work, novel aqueous biphasic systems (ABS) composed of ionic liquids (ILs) and a biocompatible polymer polypropylene glycol (400 g.mol(-1), PPG 400) were studied for the simultaneous extraction and recovery of three value-added compounds, namely, caffeine, taurine, and niacin, from expired energy drinks. ILs were designed and synthesized in order to have similar anions to the target compounds, thus allowing enhanced selectivity and biological activity, while avoiding an extra step of separation of these high-value compounds from the IL-rich phase. To this end, cholinium-based ILs comprising the anions lactate, pyruvate, taurate, and nicotinate were synthesized, and their cytotoxicity and ecotoxicity credentials were evaluated. Overall, taurine and niacin are majorly enriched in the IL-rich phase, while caffeine preferentially migrates in the majority of the cases toward the PPG-rich phase. However, caffeine also partitions to the IL-rich phase in the ABS formed by cholinium pyruvate or cholinium nicotinate. The ABS formed by cholinium nicotinate and PPG 400 is the best system identified, allowing the almost complete recovery (recovery efficiencies > 82%) of all target compounds into the IL-rich phase in one step. Furthermore, cholinium nicotinate exhibits marginal cytotoxic potential and is harmless from an ecotoxicological point of view. This system is thus a promising platform to simultaneously extract, recover, and reuse value-added compounds from expired energy drinks without the need of removing the IL or recovering the target compounds from the IL-rich phase, thus contributing to a sustainable and circular food economy.
T2  - ACS Sustainable Chemistry and Engineering
T1  - Valorization of Expired Energy Drinks by Designed and Integrated Ionic Liquid-Based Aqueous Biphasic Systems
VL  - 8
IS  - 14
SP  - 5683
EP  - 5692
DO  - 10.1021/acssuschemeng.0c00429
ER  - 

@article{
author = "Dimitrijević, Aleksandra and Tavares, Ana Paula M. and Almeida, Mafalda R. and Vraneš, Milan and Sousa, Ana C. A. and Cristovão, Ana Clara and Trtić-Petrović, Tatjana M. and Gadžurić, Slobodan and Freire, Mara G.",
year = "2020",
abstract = "Expired energy drinks are rich in bioactive value-added compounds that can be recovered and reused in order to valorize food waste within a circular economy perspective. However, to accomplish such requirements, it is necessary to develop sustainable extraction and recovery processes, which must consist of decreasing the number of steps required or developing integrated strategies. In this work, novel aqueous biphasic systems (ABS) composed of ionic liquids (ILs) and a biocompatible polymer polypropylene glycol (400 g.mol(-1), PPG 400) were studied for the simultaneous extraction and recovery of three value-added compounds, namely, caffeine, taurine, and niacin, from expired energy drinks. ILs were designed and synthesized in order to have similar anions to the target compounds, thus allowing enhanced selectivity and biological activity, while avoiding an extra step of separation of these high-value compounds from the IL-rich phase. To this end, cholinium-based ILs comprising the anions lactate, pyruvate, taurate, and nicotinate were synthesized, and their cytotoxicity and ecotoxicity credentials were evaluated. Overall, taurine and niacin are majorly enriched in the IL-rich phase, while caffeine preferentially migrates in the majority of the cases toward the PPG-rich phase. However, caffeine also partitions to the IL-rich phase in the ABS formed by cholinium pyruvate or cholinium nicotinate. The ABS formed by cholinium nicotinate and PPG 400 is the best system identified, allowing the almost complete recovery (recovery efficiencies > 82%) of all target compounds into the IL-rich phase in one step. Furthermore, cholinium nicotinate exhibits marginal cytotoxic potential and is harmless from an ecotoxicological point of view. This system is thus a promising platform to simultaneously extract, recover, and reuse value-added compounds from expired energy drinks without the need of removing the IL or recovering the target compounds from the IL-rich phase, thus contributing to a sustainable and circular food economy.",
journal = "ACS Sustainable Chemistry and Engineering",
title = "Valorization of Expired Energy Drinks by Designed and Integrated Ionic Liquid-Based Aqueous Biphasic Systems",
volume = "8",
number = "14",
pages = "5683-5692",
doi = "10.1021/acssuschemeng.0c00429"
}

Dimitrijević, A., Tavares, A. P. M., Almeida, M. R., Vraneš, M., Sousa, A. C. A., Cristovão, A. C., Trtić-Petrović, T. M., Gadžurić, S.,& Freire, M. G.. (2020). Valorization of Expired Energy Drinks by Designed and Integrated Ionic Liquid-Based Aqueous Biphasic Systems. in ACS Sustainable Chemistry and Engineering, 8(14), 5683-5692.
https://doi.org/10.1021/acssuschemeng.0c00429

Dimitrijević A, Tavares APM, Almeida MR, Vraneš M, Sousa ACA, Cristovão AC, Trtić-Petrović TM, Gadžurić S, Freire MG. Valorization of Expired Energy Drinks by Designed and Integrated Ionic Liquid-Based Aqueous Biphasic Systems. in ACS Sustainable Chemistry and Engineering. 2020;8(14):5683-5692.
doi:10.1021/acssuschemeng.0c00429 .

Dimitrijević, Aleksandra, Tavares, Ana Paula M., Almeida, Mafalda R., Vraneš, Milan, Sousa, Ana C. A., Cristovão, Ana Clara, Trtić-Petrović, Tatjana M., Gadžurić, Slobodan, Freire, Mara G., "Valorization of Expired Energy Drinks by Designed and Integrated Ionic Liquid-Based Aqueous Biphasic Systems" in ACS Sustainable Chemistry and Engineering, 8, no. 14 (2020):5683-5692,
https://doi.org/10.1021/acssuschemeng.0c00429 . .

TY  - JOUR
AU  - Dimitrijević, Aleksandra
AU  - Tavares, Ana Paula M.
AU  - Jocić, Ana
AU  - Marić, Slađana
AU  - Trtić-Petrović, Tatjana M.
AU  - Gadžurić, Slobodan
AU  - Freire, Mara G.
PY  - 2020
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8995
AB  - Aqueous biphasic systems (ABS) formed by copolymers and ionic liquids (ILs) have demonstrated to be effective separation platforms, but there is still a gap on the complete understanding of the molecular-level mechanisms ruling the two-phase formation for this type of systems. This work addresses the determination of the liquid–liquid equilibrium of ABS composed of cholinium-based salts or cholinium-based ILs and the triblock copolymer Pluronic PE6200 (PL6200). It is demonstrated that PL6200 can form ABS with all investigated cholinium-based salts or ILs, contrarily to most poly(ethylene)glycol polymers, which is due to the presence of hydrophobic propylene oxide (PO) blocks. From the phase diagrams behavior and IL/salt anions properties, it is shown that the formation of ABS with cholinium-based salts is ruled by the anions polar surface and ability to be hydrated, whereas in systems comprising ILs van der Waals interactions between the copolymer and the IL cannot be discarded. The partition of a series of alkaloids in these systems, namely caffeine, nicotine, theophylline, and theobromine, was additionally appraised. It is shown that caffeine, theophylline, and theobromine preferentially migrate to the more hydrophobic PL6200-rich phase, and that their partition depends on the water content in the respective phase, being ruled by the phases’ hydrophobicity. On the other hand, nicotine, with the most prominent hydrophobic character amongst the studied alkaloids, preferentially migrates to the salt- or IL-rich phase, in which interactions occurring between this alkaloid and the IL/salt cannot be discarded. The ABS formed by cholinium dihydrogenphosphate is the most selective system identified to separate nicotine from the remaining alkaloids, giving some insights into their investigation as separation platforms for alkaloids from natural extracts.
T2  - Separation and Purification Technology
T1  - Aqueous biphasic systems comprising copolymers and cholinium-based salts or ionic liquids: Insights on the mechanisms responsible for their creation
VL  - 248
SP  - 117050
DO  - 10.1016/j.seppur.2020.117050
ER  - 

@article{
author = "Dimitrijević, Aleksandra and Tavares, Ana Paula M. and Jocić, Ana and Marić, Slađana and Trtić-Petrović, Tatjana M. and Gadžurić, Slobodan and Freire, Mara G.",
year = "2020",
abstract = "Aqueous biphasic systems (ABS) formed by copolymers and ionic liquids (ILs) have demonstrated to be effective separation platforms, but there is still a gap on the complete understanding of the molecular-level mechanisms ruling the two-phase formation for this type of systems. This work addresses the determination of the liquid–liquid equilibrium of ABS composed of cholinium-based salts or cholinium-based ILs and the triblock copolymer Pluronic PE6200 (PL6200). It is demonstrated that PL6200 can form ABS with all investigated cholinium-based salts or ILs, contrarily to most poly(ethylene)glycol polymers, which is due to the presence of hydrophobic propylene oxide (PO) blocks. From the phase diagrams behavior and IL/salt anions properties, it is shown that the formation of ABS with cholinium-based salts is ruled by the anions polar surface and ability to be hydrated, whereas in systems comprising ILs van der Waals interactions between the copolymer and the IL cannot be discarded. The partition of a series of alkaloids in these systems, namely caffeine, nicotine, theophylline, and theobromine, was additionally appraised. It is shown that caffeine, theophylline, and theobromine preferentially migrate to the more hydrophobic PL6200-rich phase, and that their partition depends on the water content in the respective phase, being ruled by the phases’ hydrophobicity. On the other hand, nicotine, with the most prominent hydrophobic character amongst the studied alkaloids, preferentially migrates to the salt- or IL-rich phase, in which interactions occurring between this alkaloid and the IL/salt cannot be discarded. The ABS formed by cholinium dihydrogenphosphate is the most selective system identified to separate nicotine from the remaining alkaloids, giving some insights into their investigation as separation platforms for alkaloids from natural extracts.",
journal = "Separation and Purification Technology",
title = "Aqueous biphasic systems comprising copolymers and cholinium-based salts or ionic liquids: Insights on the mechanisms responsible for their creation",
volume = "248",
pages = "117050",
doi = "10.1016/j.seppur.2020.117050"
}

Dimitrijević, A., Tavares, A. P. M., Jocić, A., Marić, S., Trtić-Petrović, T. M., Gadžurić, S.,& Freire, M. G.. (2020). Aqueous biphasic systems comprising copolymers and cholinium-based salts or ionic liquids: Insights on the mechanisms responsible for their creation. in Separation and Purification Technology, 248, 117050.
https://doi.org/10.1016/j.seppur.2020.117050

Dimitrijević A, Tavares APM, Jocić A, Marić S, Trtić-Petrović TM, Gadžurić S, Freire MG. Aqueous biphasic systems comprising copolymers and cholinium-based salts or ionic liquids: Insights on the mechanisms responsible for their creation. in Separation and Purification Technology. 2020;248:117050.
doi:10.1016/j.seppur.2020.117050 .

Dimitrijević, Aleksandra, Tavares, Ana Paula M., Jocić, Ana, Marić, Slađana, Trtić-Petrović, Tatjana M., Gadžurić, Slobodan, Freire, Mara G., "Aqueous biphasic systems comprising copolymers and cholinium-based salts or ionic liquids: Insights on the mechanisms responsible for their creation" in Separation and Purification Technology, 248 (2020):117050,
https://doi.org/10.1016/j.seppur.2020.117050 . .

TY  - JOUR
AU  - Dimitrijević, Aleksandra
AU  - Jocić, Ana
AU  - Zec, Nebojša
AU  - Tot, Aleksandar
AU  - Papović, Snežana
AU  - Gadžurić, Slobodan
AU  - Vraneš, Milan
AU  - Trtić-Petrović, Tatjana M.
PY  - 2019
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8157
AB  - The novel aqueous biphasic systems based on symmetric imidazolium ionic liquids (IL-ABSs)for the extraction of toxic and resistive dyes from water was studied. The cation symmetricity of ILs strongly influence the outstanding ability of 1,3-dibutylimidazolium dicyanamide, [bbim][dca], to generate ABS with the exceptionally low amount of eco-friendly citrate salt. A remarkable potential of [bbim][dca]/citrate based ABS to remove Orange II from wastewater with concentration up to 1000 fold and efficiency above 99.4% in a single step was achieved. The improved safety of proposed method nominates it as promising future strategy for pollution prevention. © 2019 The Korean Society of Industrial and Engineering Chemistry
T2  - Journal of Industrial and Engineering Chemistry
T1  - Improved single-step extraction performance of aqueous biphasic systems using novel symmetric ionic liquids for the decolorisation of toxic dye effluents
VL  - 76
SP  - 500
EP  - 507
DO  - 10.1016/j.jiec.2019.04.017
ER  - 

@article{
author = "Dimitrijević, Aleksandra and Jocić, Ana and Zec, Nebojša and Tot, Aleksandar and Papović, Snežana and Gadžurić, Slobodan and Vraneš, Milan and Trtić-Petrović, Tatjana M.",
year = "2019",
abstract = "The novel aqueous biphasic systems based on symmetric imidazolium ionic liquids (IL-ABSs)for the extraction of toxic and resistive dyes from water was studied. The cation symmetricity of ILs strongly influence the outstanding ability of 1,3-dibutylimidazolium dicyanamide, [bbim][dca], to generate ABS with the exceptionally low amount of eco-friendly citrate salt. A remarkable potential of [bbim][dca]/citrate based ABS to remove Orange II from wastewater with concentration up to 1000 fold and efficiency above 99.4% in a single step was achieved. The improved safety of proposed method nominates it as promising future strategy for pollution prevention. © 2019 The Korean Society of Industrial and Engineering Chemistry",
journal = "Journal of Industrial and Engineering Chemistry",
title = "Improved single-step extraction performance of aqueous biphasic systems using novel symmetric ionic liquids for the decolorisation of toxic dye effluents",
volume = "76",
pages = "500-507",
doi = "10.1016/j.jiec.2019.04.017"
}

Dimitrijević, A., Jocić, A., Zec, N., Tot, A., Papović, S., Gadžurić, S., Vraneš, M.,& Trtić-Petrović, T. M.. (2019). Improved single-step extraction performance of aqueous biphasic systems using novel symmetric ionic liquids for the decolorisation of toxic dye effluents. in Journal of Industrial and Engineering Chemistry, 76, 500-507.
https://doi.org/10.1016/j.jiec.2019.04.017

Dimitrijević A, Jocić A, Zec N, Tot A, Papović S, Gadžurić S, Vraneš M, Trtić-Petrović TM. Improved single-step extraction performance of aqueous biphasic systems using novel symmetric ionic liquids for the decolorisation of toxic dye effluents. in Journal of Industrial and Engineering Chemistry. 2019;76:500-507.
doi:10.1016/j.jiec.2019.04.017 .

Dimitrijević, Aleksandra, Jocić, Ana, Zec, Nebojša, Tot, Aleksandar, Papović, Snežana, Gadžurić, Slobodan, Vraneš, Milan, Trtić-Petrović, Tatjana M., "Improved single-step extraction performance of aqueous biphasic systems using novel symmetric ionic liquids for the decolorisation of toxic dye effluents" in Journal of Industrial and Engineering Chemistry, 76 (2019):500-507,
https://doi.org/10.1016/j.jiec.2019.04.017 . .

TY  - JOUR
AU  - Dimitrijević, Aleksandra
AU  - Jocić, Ana
AU  - Zec, Nebojša
AU  - Tot, Aleksandar
AU  - Papović, Snežana
AU  - Gadžurić, Slobodan
AU  - Vraneš, Milan
AU  - Trtić-Petrović, Tatjana M.
PY  - 2019
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8168
AB  - The novel aqueous biphasic systems based on symmetric imidazolium ionic liquids (IL-ABSs)for the extraction of toxic and resistive dyes from water was studied. The cation symmetricity of ILs strongly influence the outstanding ability of 1,3-dibutylimidazolium dicyanamide, [bbim][dca], to generate ABS with the exceptionally low amount of eco-friendly citrate salt. A remarkable potential of [bbim][dca]/citrate based ABS to remove Orange II from wastewater with concentration up to 1000 fold and efficiency above 99.4% in a single step was achieved. The improved safety of proposed method nominates it as promising future strategy for pollution prevention.
T2  - Journal of Industrial and Engineering Chemistry
T1  - Improved single-step extraction performance of aqueous biphasic systems using novel symmetric ionic liquids for the decolorisation of toxic dye effluents
VL  - 76
SP  - 500
EP  - 507
DO  - 10.1016/j.jiec.2019.04.017
ER  - 

@article{
author = "Dimitrijević, Aleksandra and Jocić, Ana and Zec, Nebojša and Tot, Aleksandar and Papović, Snežana and Gadžurić, Slobodan and Vraneš, Milan and Trtić-Petrović, Tatjana M.",
year = "2019",
abstract = "The novel aqueous biphasic systems based on symmetric imidazolium ionic liquids (IL-ABSs)for the extraction of toxic and resistive dyes from water was studied. The cation symmetricity of ILs strongly influence the outstanding ability of 1,3-dibutylimidazolium dicyanamide, [bbim][dca], to generate ABS with the exceptionally low amount of eco-friendly citrate salt. A remarkable potential of [bbim][dca]/citrate based ABS to remove Orange II from wastewater with concentration up to 1000 fold and efficiency above 99.4% in a single step was achieved. The improved safety of proposed method nominates it as promising future strategy for pollution prevention.",
journal = "Journal of Industrial and Engineering Chemistry",
title = "Improved single-step extraction performance of aqueous biphasic systems using novel symmetric ionic liquids for the decolorisation of toxic dye effluents",
volume = "76",
pages = "500-507",
doi = "10.1016/j.jiec.2019.04.017"
}

Dimitrijević, A., Jocić, A., Zec, N., Tot, A., Papović, S., Gadžurić, S., Vraneš, M.,& Trtić-Petrović, T. M.. (2019). Improved single-step extraction performance of aqueous biphasic systems using novel symmetric ionic liquids for the decolorisation of toxic dye effluents. in Journal of Industrial and Engineering Chemistry, 76, 500-507.
https://doi.org/10.1016/j.jiec.2019.04.017

Dimitrijević A, Jocić A, Zec N, Tot A, Papović S, Gadžurić S, Vraneš M, Trtić-Petrović TM. Improved single-step extraction performance of aqueous biphasic systems using novel symmetric ionic liquids for the decolorisation of toxic dye effluents. in Journal of Industrial and Engineering Chemistry. 2019;76:500-507.
doi:10.1016/j.jiec.2019.04.017 .

Dimitrijević, Aleksandra, Jocić, Ana, Zec, Nebojša, Tot, Aleksandar, Papović, Snežana, Gadžurić, Slobodan, Vraneš, Milan, Trtić-Petrović, Tatjana M., "Improved single-step extraction performance of aqueous biphasic systems using novel symmetric ionic liquids for the decolorisation of toxic dye effluents" in Journal of Industrial and Engineering Chemistry, 76 (2019):500-507,
https://doi.org/10.1016/j.jiec.2019.04.017 . .

TY  - JOUR
AU  - Vraneš, Milan
AU  - Panić, Jovana
AU  - Tot, Aleksandar
AU  - Popsavin, Mirjana
AU  - Jocić, Ana
AU  - Gadžurić, Slobodan
PY  - 2019
UR  - https://linkinghub.elsevier.com/retrieve/pii/S0021961418307808
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7943
AB  - In this paper, physicochemical characterization of newly synthesized choline based ionic liquids with five different chelating anions were examined. The ionic liquids (ILs): cholinium-L-lactate, [Ch][Lac], cholinium-picolinate, [Ch][Pic], cholinium-anthranilate, [Ch][Ant], cholinium-oxyquinolinate, [Ch][oQ], and cholinium-diethylenetriaminepentaacetate, [Ch]3[DTPA], were prepared for the first time and their structures were confirmed by IR and 1H and 13C NMR spectra. Also, thermogravimetric analysis (TGA) was applied to determine their thermal stabilities. Based on the measured density values and viscosity in the temperature range from (293.15 to 323.15) K and calculated values of thermal expansion coefficients and activation energy of viscous flow, as well as of computational simulations, the interactions and structures of the investigated ionic liquids were discussed. © 2018 Elsevier Ltd
T2  - The Journal of Chemical Thermodynamics
T1  - Physicochemical characterization of choline based ionic liquids with chelating anions
VL  - 131
SP  - 80
EP  - 87
DO  - 10.1016/j.jct.2018.10.026
ER  - 

@article{
author = "Vraneš, Milan and Panić, Jovana and Tot, Aleksandar and Popsavin, Mirjana and Jocić, Ana and Gadžurić, Slobodan",
year = "2019",
abstract = "In this paper, physicochemical characterization of newly synthesized choline based ionic liquids with five different chelating anions were examined. The ionic liquids (ILs): cholinium-L-lactate, [Ch][Lac], cholinium-picolinate, [Ch][Pic], cholinium-anthranilate, [Ch][Ant], cholinium-oxyquinolinate, [Ch][oQ], and cholinium-diethylenetriaminepentaacetate, [Ch]3[DTPA], were prepared for the first time and their structures were confirmed by IR and 1H and 13C NMR spectra. Also, thermogravimetric analysis (TGA) was applied to determine their thermal stabilities. Based on the measured density values and viscosity in the temperature range from (293.15 to 323.15) K and calculated values of thermal expansion coefficients and activation energy of viscous flow, as well as of computational simulations, the interactions and structures of the investigated ionic liquids were discussed. © 2018 Elsevier Ltd",
journal = "The Journal of Chemical Thermodynamics",
title = "Physicochemical characterization of choline based ionic liquids with chelating anions",
volume = "131",
pages = "80-87",
doi = "10.1016/j.jct.2018.10.026"
}

Vraneš, M., Panić, J., Tot, A., Popsavin, M., Jocić, A.,& Gadžurić, S.. (2019). Physicochemical characterization of choline based ionic liquids with chelating anions. in The Journal of Chemical Thermodynamics, 131, 80-87.
https://doi.org/10.1016/j.jct.2018.10.026

Vraneš M, Panić J, Tot A, Popsavin M, Jocić A, Gadžurić S. Physicochemical characterization of choline based ionic liquids with chelating anions. in The Journal of Chemical Thermodynamics. 2019;131:80-87.
doi:10.1016/j.jct.2018.10.026 .

Vraneš, Milan, Panić, Jovana, Tot, Aleksandar, Popsavin, Mirjana, Jocić, Ana, Gadžurić, Slobodan, "Physicochemical characterization of choline based ionic liquids with chelating anions" in The Journal of Chemical Thermodynamics, 131 (2019):80-87,
https://doi.org/10.1016/j.jct.2018.10.026 . .

TY  - JOUR
AU  - Zec, Nebojša
AU  - Vraneš, Milan
AU  - Bešter-Rogač, Marija
AU  - Trtić-Petrović, Tatjana M.
AU  - Dimitrijević, Aleksandra
AU  - Čobanov, Isidora
AU  - Gadžurić, Slobodan
PY  - 2018
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7660
AB  - In this manuscript eight new 1,3-dialkylimidazolium bromide ionic liquids, {[}CnCmim]{[}Br], were synthesized and characterized. Densities of ionic liquids and their diluted aqueous solutions have been measured over the whole composition range at selected temperatures from (293.15 to 323.15) K and at atmospheric pressure (p = 0.1 MPa). Influence of alkyl chain length and cation symmetry on densities and volumetric properties as well as nature of the interactions in aqueous {[}CnCmim]{[}Br] solutions have been discussed and compared with previously published aqueous {[}C(2)C(4)im]{[}Br] system. Densities of pure bromide based ionic liquids decrease with increasing alkyl chain length on imidazolium cation and depend on total number of methyl group in both side alkyl chains. Apparent molar volumes at infinite dilution of investigated ionic liquids in water increase linearly with increase of the total number of the C atoms in the side alkyl chain. (C) 2018 Elsevier Ltd.
T2  - The Journal of Chemical Thermodynamics
T1  - Influence of the alkyl chain length on densities and volumetric properties of 1,3-dialkylimidazolium bromide ionic liquids and their aqueous solutions
VL  - 121
SP  - 72
EP  - 78
DO  - 10.1016/j.jct.2018.02.001
ER  - 

@article{
author = "Zec, Nebojša and Vraneš, Milan and Bešter-Rogač, Marija and Trtić-Petrović, Tatjana M. and Dimitrijević, Aleksandra and Čobanov, Isidora and Gadžurić, Slobodan",
year = "2018",
abstract = "In this manuscript eight new 1,3-dialkylimidazolium bromide ionic liquids, {[}CnCmim]{[}Br], were synthesized and characterized. Densities of ionic liquids and their diluted aqueous solutions have been measured over the whole composition range at selected temperatures from (293.15 to 323.15) K and at atmospheric pressure (p = 0.1 MPa). Influence of alkyl chain length and cation symmetry on densities and volumetric properties as well as nature of the interactions in aqueous {[}CnCmim]{[}Br] solutions have been discussed and compared with previously published aqueous {[}C(2)C(4)im]{[}Br] system. Densities of pure bromide based ionic liquids decrease with increasing alkyl chain length on imidazolium cation and depend on total number of methyl group in both side alkyl chains. Apparent molar volumes at infinite dilution of investigated ionic liquids in water increase linearly with increase of the total number of the C atoms in the side alkyl chain. (C) 2018 Elsevier Ltd.",
journal = "The Journal of Chemical Thermodynamics",
title = "Influence of the alkyl chain length on densities and volumetric properties of 1,3-dialkylimidazolium bromide ionic liquids and their aqueous solutions",
volume = "121",
pages = "72-78",
doi = "10.1016/j.jct.2018.02.001"
}

Zec, N., Vraneš, M., Bešter-Rogač, M., Trtić-Petrović, T. M., Dimitrijević, A., Čobanov, I.,& Gadžurić, S.. (2018). Influence of the alkyl chain length on densities and volumetric properties of 1,3-dialkylimidazolium bromide ionic liquids and their aqueous solutions. in The Journal of Chemical Thermodynamics, 121, 72-78.
https://doi.org/10.1016/j.jct.2018.02.001

Zec N, Vraneš M, Bešter-Rogač M, Trtić-Petrović TM, Dimitrijević A, Čobanov I, Gadžurić S. Influence of the alkyl chain length on densities and volumetric properties of 1,3-dialkylimidazolium bromide ionic liquids and their aqueous solutions. in The Journal of Chemical Thermodynamics. 2018;121:72-78.
doi:10.1016/j.jct.2018.02.001 .

Zec, Nebojša, Vraneš, Milan, Bešter-Rogač, Marija, Trtić-Petrović, Tatjana M., Dimitrijević, Aleksandra, Čobanov, Isidora, Gadžurić, Slobodan, "Influence of the alkyl chain length on densities and volumetric properties of 1,3-dialkylimidazolium bromide ionic liquids and their aqueous solutions" in The Journal of Chemical Thermodynamics, 121 (2018):72-78,
https://doi.org/10.1016/j.jct.2018.02.001 . .

TY  - JOUR
AU  - Trtić-Petrović, Tatjana M.
AU  - Dimitrijević, Aleksandra
AU  - Zdolšek, Nikola
AU  - Đorđević, Jelena S.
AU  - Tot, Aleksandar
AU  - Vraneš, Milan
AU  - Gadžurić, Slobodan
PY  - 2018
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1891
AB  - In this study, four hydrophilic ionic liquids (ILs) containing 1-alkyl-3-methylimidazolim cation and either salicylate or chloride anions were synthetized and studied as new task-specific ionic liquids (TSILs) suitable for aqueous biphasic system (ABS) formation and selective one-step extraction of copper(II). TSILs are designed so that the anion is responsible for forming the complex with metal(II) and preventing hydrolysis of metal cations at very strong alkaline pH, whereas the cation is responsible for selective extraction of metal(II)-salicylate complexes. It was found that 1-butyl-3-methylimidazolium salicylate could be used for selective extraction of Cu(II) in the presence of Zn(II), Cd(II), and Pb(II) at very alkaline solution without metal hydroxide formation. It was assumed that formation of metal(II)-salicylate complexes prevents the hydrolysis of the metal ions in alkaline solutions. The determined stability constants for Cu(II)-salicylate complexes, where salicylate was derived from different ionic liquids, indicated that there was no significant influence of the cation of the ionic liquid on the stability of the complexes. The ABS based on 1-butyl-3-methylimidazolium salicylate has been applied as the sample preparation step prior to voltammetric determination of Cu(II). The effect of volume of aqueous sample and IL and extraction time were investigated and optimum extraction conditions were determined. The obtained detection limits were 8 ng dm(-3). The optimized method was applied for the determination of Cu(II) in tap water, wastewater, and urine. The study indicated that application of the ABS based on 1-butyl-3-methylimidazolium salicylate ionic liquid could be successfully applied as the sample preparation method for the determination of Cu(II) from various environmental samples.
T2  - Analytical and Bioanalytical Chemistry
T1  - New sample preparation method based on task-specific ionic liquids for extraction and determination of copper in urine and wastewater
VL  - 410
IS  - 1
SP  - 155
EP  - 166
DO  - 10.1007/s00216-017-0705-z
ER  - 

@article{
author = "Trtić-Petrović, Tatjana M. and Dimitrijević, Aleksandra and Zdolšek, Nikola and Đorđević, Jelena S. and Tot, Aleksandar and Vraneš, Milan and Gadžurić, Slobodan",
year = "2018",
abstract = "In this study, four hydrophilic ionic liquids (ILs) containing 1-alkyl-3-methylimidazolim cation and either salicylate or chloride anions were synthetized and studied as new task-specific ionic liquids (TSILs) suitable for aqueous biphasic system (ABS) formation and selective one-step extraction of copper(II). TSILs are designed so that the anion is responsible for forming the complex with metal(II) and preventing hydrolysis of metal cations at very strong alkaline pH, whereas the cation is responsible for selective extraction of metal(II)-salicylate complexes. It was found that 1-butyl-3-methylimidazolium salicylate could be used for selective extraction of Cu(II) in the presence of Zn(II), Cd(II), and Pb(II) at very alkaline solution without metal hydroxide formation. It was assumed that formation of metal(II)-salicylate complexes prevents the hydrolysis of the metal ions in alkaline solutions. The determined stability constants for Cu(II)-salicylate complexes, where salicylate was derived from different ionic liquids, indicated that there was no significant influence of the cation of the ionic liquid on the stability of the complexes. The ABS based on 1-butyl-3-methylimidazolium salicylate has been applied as the sample preparation step prior to voltammetric determination of Cu(II). The effect of volume of aqueous sample and IL and extraction time were investigated and optimum extraction conditions were determined. The obtained detection limits were 8 ng dm(-3). The optimized method was applied for the determination of Cu(II) in tap water, wastewater, and urine. The study indicated that application of the ABS based on 1-butyl-3-methylimidazolium salicylate ionic liquid could be successfully applied as the sample preparation method for the determination of Cu(II) from various environmental samples.",
journal = "Analytical and Bioanalytical Chemistry",
title = "New sample preparation method based on task-specific ionic liquids for extraction and determination of copper in urine and wastewater",
volume = "410",
number = "1",
pages = "155-166",
doi = "10.1007/s00216-017-0705-z"
}

Trtić-Petrović, T. M., Dimitrijević, A., Zdolšek, N., Đorđević, J. S., Tot, A., Vraneš, M.,& Gadžurić, S.. (2018). New sample preparation method based on task-specific ionic liquids for extraction and determination of copper in urine and wastewater. in Analytical and Bioanalytical Chemistry, 410(1), 155-166.
https://doi.org/10.1007/s00216-017-0705-z

Trtić-Petrović TM, Dimitrijević A, Zdolšek N, Đorđević JS, Tot A, Vraneš M, Gadžurić S. New sample preparation method based on task-specific ionic liquids for extraction and determination of copper in urine and wastewater. in Analytical and Bioanalytical Chemistry. 2018;410(1):155-166.
doi:10.1007/s00216-017-0705-z .

Trtić-Petrović, Tatjana M., Dimitrijević, Aleksandra, Zdolšek, Nikola, Đorđević, Jelena S., Tot, Aleksandar, Vraneš, Milan, Gadžurić, Slobodan, "New sample preparation method based on task-specific ionic liquids for extraction and determination of copper in urine and wastewater" in Analytical and Bioanalytical Chemistry, 410, no. 1 (2018):155-166,
https://doi.org/10.1007/s00216-017-0705-z . .

TY  - JOUR
AU  - Dimitrijević, Aleksandra
AU  - Ignjatović, Ljubiša M.
AU  - Tot, Aleksandar
AU  - Vraneš, Milan
AU  - Zec, Nebojša
AU  - Gadžurić, Slobodan
AU  - Trtić-Petrović, Tatjana M.
PY  - 2017
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1776
AB  - In this paper we report a simultaneous one-step extraction of five pesticides (acetamiprid, imidaclopride, simazine, linuron and tebufenozide) of different polarity using aqueous biphasic system based on 1-butyl-3(methyl or ethyl) substituted imidazolium or pyrrolidinium ionic liquids with bromide or dicyanamide anion and potassium carbonate as a salting-out agent. Experimentally data obtained for the ternary system (ionic liquid + K2CO3 + H2O) were fitted and correlated by Merchuk equation with satisfactory high correlation factor. The effect of the cation alkyl chain length and the variation of anions of the ionic liquid on the aqueous biphasic system formation and the efficiency of pesticide extraction were investigated. Complete extraction of all studied pesticides was obtained applying aqueous biphasic system based on 1-butyl-3-ethyl imidazolium dicyanamide. It was shown that simultaneous extraction of the different polarity pesticides is achieved in a single-step procedure applying properly tailored ionic liquids in the aqueous biphasic system formulation. In order to explain excellent extraction of the polar pesticides in the studied aqueous biphasic systems, molecular dynamics was applied and the binding energies and non-covalent interactions were calculated. It was found that 1-butyl-3-ethyl imidazolium dicyanamide achieves the strongest interactions with the polar pesticides (acetamiprid and imidaclopride) leading to the highest partition coefficients. It was shown that combination of experimental and computational approach can be successfully applied for the selection and design of suitable ionic liquids for efficient extraction of various polarity pesticides using simple aqueous biphasic ionic liquid based systems. (C) 2017 Elsevier B.V. All rights reserved.
T2  - Journal of Molecular Liquids
T1  - Simultaneous extraction of pesticides of different polarity applying aqueous biphasic systems based on ionic liquids
VL  - 243
SP  - 646
EP  - 653
DO  - 10.1016/j.molliq.2017.08.077
ER  - 

@article{
author = "Dimitrijević, Aleksandra and Ignjatović, Ljubiša M. and Tot, Aleksandar and Vraneš, Milan and Zec, Nebojša and Gadžurić, Slobodan and Trtić-Petrović, Tatjana M.",
year = "2017",
abstract = "In this paper we report a simultaneous one-step extraction of five pesticides (acetamiprid, imidaclopride, simazine, linuron and tebufenozide) of different polarity using aqueous biphasic system based on 1-butyl-3(methyl or ethyl) substituted imidazolium or pyrrolidinium ionic liquids with bromide or dicyanamide anion and potassium carbonate as a salting-out agent. Experimentally data obtained for the ternary system (ionic liquid + K2CO3 + H2O) were fitted and correlated by Merchuk equation with satisfactory high correlation factor. The effect of the cation alkyl chain length and the variation of anions of the ionic liquid on the aqueous biphasic system formation and the efficiency of pesticide extraction were investigated. Complete extraction of all studied pesticides was obtained applying aqueous biphasic system based on 1-butyl-3-ethyl imidazolium dicyanamide. It was shown that simultaneous extraction of the different polarity pesticides is achieved in a single-step procedure applying properly tailored ionic liquids in the aqueous biphasic system formulation. In order to explain excellent extraction of the polar pesticides in the studied aqueous biphasic systems, molecular dynamics was applied and the binding energies and non-covalent interactions were calculated. It was found that 1-butyl-3-ethyl imidazolium dicyanamide achieves the strongest interactions with the polar pesticides (acetamiprid and imidaclopride) leading to the highest partition coefficients. It was shown that combination of experimental and computational approach can be successfully applied for the selection and design of suitable ionic liquids for efficient extraction of various polarity pesticides using simple aqueous biphasic ionic liquid based systems. (C) 2017 Elsevier B.V. All rights reserved.",
journal = "Journal of Molecular Liquids",
title = "Simultaneous extraction of pesticides of different polarity applying aqueous biphasic systems based on ionic liquids",
volume = "243",
pages = "646-653",
doi = "10.1016/j.molliq.2017.08.077"
}

Dimitrijević, A., Ignjatović, L. M., Tot, A., Vraneš, M., Zec, N., Gadžurić, S.,& Trtić-Petrović, T. M.. (2017). Simultaneous extraction of pesticides of different polarity applying aqueous biphasic systems based on ionic liquids. in Journal of Molecular Liquids, 243, 646-653.
https://doi.org/10.1016/j.molliq.2017.08.077

Dimitrijević A, Ignjatović LM, Tot A, Vraneš M, Zec N, Gadžurić S, Trtić-Petrović TM. Simultaneous extraction of pesticides of different polarity applying aqueous biphasic systems based on ionic liquids. in Journal of Molecular Liquids. 2017;243:646-653.
doi:10.1016/j.molliq.2017.08.077 .

Dimitrijević, Aleksandra, Ignjatović, Ljubiša M., Tot, Aleksandar, Vraneš, Milan, Zec, Nebojša, Gadžurić, Slobodan, Trtić-Petrović, Tatjana M., "Simultaneous extraction of pesticides of different polarity applying aqueous biphasic systems based on ionic liquids" in Journal of Molecular Liquids, 243 (2017):646-653,
https://doi.org/10.1016/j.molliq.2017.08.077 . .

TY  - JOUR
AU  - Đorđević, Jelena S.
AU  - Maksimović, Vesna
AU  - Gadžurić, Slobodan
AU  - Trtić-Petrović, Tatjana M.
PY  - 2017
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1623
AB  - A new method for the electroanalytical determination of carbendazim is reported using a novel ionic liquid-based carbon paste electrode. 1-hexyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide, 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide, and 1-butyl-1-methylpyrrolidinium bis(trifluoromethyl-sulfonyl)imide were used as additives in the paste for electrode fabrication. The electrodes were characterized by cyclic voltammetry of the http://www.w3.org/1999/xlink couple and scanning electron microscopy. The carbon paste electrode containing 19% 1-hexyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide was selected for the electrochemical determination of carbendazim by differential pulse adsorptive stripping voltammetry. The influence of electrolyte pH, accumulation potential and time, and the presence of selected pesticides on electrochemical behavior of carbendazim were characterized. The optimal conditions for differential pulse adsorptive stripping voltammetry of carbendazim were determined to be a pH 5.0 Britton-Robinson buffer, an accumulation potential of -0.05V, an accumulation time of 120s, a start potential of -0.10V vs. the reference; an end potential of +1.30V, and a scan rate of 0.050Vs(-1). The linear dynamic range of the method was from 0.010 to 0.247mgL(-1) with a correlation coefficient of 0.9995. The recovery was 104.1% in fortified tap water, demonstrating its suitability for the analysis of water.
T2  - Analytical Letters
T1  - Determination of Carbendazim by an Ionic Liquid-Modified Carbon Paste Electrode
VL  - 50
IS  - 7
SP  - 1075
EP  - 1090
DO  - 10.1080/00032719.2016.1210615
ER  - 

@article{
author = "Đorđević, Jelena S. and Maksimović, Vesna and Gadžurić, Slobodan and Trtić-Petrović, Tatjana M.",
year = "2017",
abstract = "A new method for the electroanalytical determination of carbendazim is reported using a novel ionic liquid-based carbon paste electrode. 1-hexyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide, 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide, and 1-butyl-1-methylpyrrolidinium bis(trifluoromethyl-sulfonyl)imide were used as additives in the paste for electrode fabrication. The electrodes were characterized by cyclic voltammetry of the http://www.w3.org/1999/xlink couple and scanning electron microscopy. The carbon paste electrode containing 19% 1-hexyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide was selected for the electrochemical determination of carbendazim by differential pulse adsorptive stripping voltammetry. The influence of electrolyte pH, accumulation potential and time, and the presence of selected pesticides on electrochemical behavior of carbendazim were characterized. The optimal conditions for differential pulse adsorptive stripping voltammetry of carbendazim were determined to be a pH 5.0 Britton-Robinson buffer, an accumulation potential of -0.05V, an accumulation time of 120s, a start potential of -0.10V vs. the reference; an end potential of +1.30V, and a scan rate of 0.050Vs(-1). The linear dynamic range of the method was from 0.010 to 0.247mgL(-1) with a correlation coefficient of 0.9995. The recovery was 104.1% in fortified tap water, demonstrating its suitability for the analysis of water.",
journal = "Analytical Letters",
title = "Determination of Carbendazim by an Ionic Liquid-Modified Carbon Paste Electrode",
volume = "50",
number = "7",
pages = "1075-1090",
doi = "10.1080/00032719.2016.1210615"
}

Đorđević, J. S., Maksimović, V., Gadžurić, S.,& Trtić-Petrović, T. M.. (2017). Determination of Carbendazim by an Ionic Liquid-Modified Carbon Paste Electrode. in Analytical Letters, 50(7), 1075-1090.
https://doi.org/10.1080/00032719.2016.1210615

Đorđević JS, Maksimović V, Gadžurić S, Trtić-Petrović TM. Determination of Carbendazim by an Ionic Liquid-Modified Carbon Paste Electrode. in Analytical Letters. 2017;50(7):1075-1090.
doi:10.1080/00032719.2016.1210615 .

Đorđević, Jelena S., Maksimović, Vesna, Gadžurić, Slobodan, Trtić-Petrović, Tatjana M., "Determination of Carbendazim by an Ionic Liquid-Modified Carbon Paste Electrode" in Analytical Letters, 50, no. 7 (2017):1075-1090,
https://doi.org/10.1080/00032719.2016.1210615 . .

TY  - JOUR
AU  - Dimitrijević, Aleksandra
AU  - Trtić-Petrović, Tatjana M.
AU  - Vraneš, Milan
AU  - Papović, Snežana
AU  - Tot, Aleksandar
AU  - Dožić, Sanja
AU  - Gadžurić, Slobodan
PY  - 2016
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/899
AB  - In this work, novel phase diagrams for aqueous solutions of 1-alkyl-3-methylimidazolium- and 1-butyl-3-ethylimidazolium-based ILs combined with phosphate-based salts, namely, K3PO4 or K2HPO4, are reported and discussed. To correlate the binodal data, the Merchuk equation is applied. The tie lines and tie-line lengths are also presented. The anion influence on the ability to form aqueous biphasic system (ABS) is investigated for the IL with the same1-butyl-3-methylimidazolium cation, [bmim](+), and various anions, for example, salicylate, [SAL](-); trifluoromethanesulfonate, [TFS](-); dicyanamide, [DCA](-); and chloride, [Cl](-). The order of studied anions to form ABS is [TFS](-) GT [SAL](-) GT [DCA](-) GT [Cl](-). The effect of alkyl chain length on imidazolium ion on liquidliquid equilibrium is discussed in terms of increasing ionic liquid hydrophobicity and poorer affinity for water. It is shown that 1-hexyl-3-methylimidazolium chloride ionic liquid has a better ability to form ABS comparing to ionic liquid with butyl chain and the same anion. Newly synthesized ionic-liquid-containing ethyl group 1-butyl-3-ethylimidazolium bromide was also investigated, showing the influence of both ethyl group and bromide anion on the ability of ABS formation.
T2  - Journal of Chemical and Engineering Data
T1  - Liquid-Liquid Equilibria in Aqueous 1-Alkyl-3-methylimidazolium- and 1-Butyl-3-ethylimidazolium-Based Ionic Liquids
VL  - 61
IS  - 1
SP  - 549
EP  - 555
DO  - 10.1021/acs.jced.5b00697
ER  - 

@article{
author = "Dimitrijević, Aleksandra and Trtić-Petrović, Tatjana M. and Vraneš, Milan and Papović, Snežana and Tot, Aleksandar and Dožić, Sanja and Gadžurić, Slobodan",
year = "2016",
abstract = "In this work, novel phase diagrams for aqueous solutions of 1-alkyl-3-methylimidazolium- and 1-butyl-3-ethylimidazolium-based ILs combined with phosphate-based salts, namely, K3PO4 or K2HPO4, are reported and discussed. To correlate the binodal data, the Merchuk equation is applied. The tie lines and tie-line lengths are also presented. The anion influence on the ability to form aqueous biphasic system (ABS) is investigated for the IL with the same1-butyl-3-methylimidazolium cation, [bmim](+), and various anions, for example, salicylate, [SAL](-); trifluoromethanesulfonate, [TFS](-); dicyanamide, [DCA](-); and chloride, [Cl](-). The order of studied anions to form ABS is [TFS](-) GT [SAL](-) GT [DCA](-) GT [Cl](-). The effect of alkyl chain length on imidazolium ion on liquidliquid equilibrium is discussed in terms of increasing ionic liquid hydrophobicity and poorer affinity for water. It is shown that 1-hexyl-3-methylimidazolium chloride ionic liquid has a better ability to form ABS comparing to ionic liquid with butyl chain and the same anion. Newly synthesized ionic-liquid-containing ethyl group 1-butyl-3-ethylimidazolium bromide was also investigated, showing the influence of both ethyl group and bromide anion on the ability of ABS formation.",
journal = "Journal of Chemical and Engineering Data",
title = "Liquid-Liquid Equilibria in Aqueous 1-Alkyl-3-methylimidazolium- and 1-Butyl-3-ethylimidazolium-Based Ionic Liquids",
volume = "61",
number = "1",
pages = "549-555",
doi = "10.1021/acs.jced.5b00697"
}

Dimitrijević, A., Trtić-Petrović, T. M., Vraneš, M., Papović, S., Tot, A., Dožić, S.,& Gadžurić, S.. (2016). Liquid-Liquid Equilibria in Aqueous 1-Alkyl-3-methylimidazolium- and 1-Butyl-3-ethylimidazolium-Based Ionic Liquids. in Journal of Chemical and Engineering Data, 61(1), 549-555.
https://doi.org/10.1021/acs.jced.5b00697

Dimitrijević A, Trtić-Petrović TM, Vraneš M, Papović S, Tot A, Dožić S, Gadžurić S. Liquid-Liquid Equilibria in Aqueous 1-Alkyl-3-methylimidazolium- and 1-Butyl-3-ethylimidazolium-Based Ionic Liquids. in Journal of Chemical and Engineering Data. 2016;61(1):549-555.
doi:10.1021/acs.jced.5b00697 .

Dimitrijević, Aleksandra, Trtić-Petrović, Tatjana M., Vraneš, Milan, Papović, Snežana, Tot, Aleksandar, Dožić, Sanja, Gadžurić, Slobodan, "Liquid-Liquid Equilibria in Aqueous 1-Alkyl-3-methylimidazolium- and 1-Butyl-3-ethylimidazolium-Based Ionic Liquids" in Journal of Chemical and Engineering Data, 61, no. 1 (2016):549-555,
https://doi.org/10.1021/acs.jced.5b00697 . .

TY  - JOUR
AU  - Dimitrijević, Aleksandra
AU  - Zec, Nebojša
AU  - Zdolšek, Nikola
AU  - Dožić, Sanja
AU  - Tot, Aleksandar
AU  - Gadžurić, Slobodan
AU  - Vraneš, Milan
AU  - Trtić-Petrović, Tatjana M.
PY  - 2016
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1213
AB  - In this work three 1-alkyl-3-ethylimidazolium bromide ionic liquids (alkyl = ethyl, hexyl and octyl) were synthesized applying both, conventional and microwave assisted synthetic paths. The phase diagrams for aqueous solutions of 1-alkyl-3-ethylimidazolium bromide ionic liquids as novel extractants combined with phosphate-based salts are reported and discussed in terms of aqueous biphasic system (ABS) formation. Merchuk equation was applied in order to correlate the,experimental binodal data. The liquid-liquid equilibrium data (tie-line compositions and tie-line length) were also experimentally determined by a gravimetric method. The influence of the alkyl chain length on ABS formation ability was investigated. It was found that ability to form ABS increases with the increase of the alkyl chain length on the imidazolium cation. Also, it was found that ionic liquids with ethyl group in the N-3 position better form ABS compared to those with methyl substituent. This was discussed in terms of increasing ionic liquid hydrophobicity and poor affinity for water. In order to better understand the impact of the alkyl side chain of the imidazolium ion and the efficiency of ABS formation, computer simulations were performed using investigated ionic liquids with the ethyl group in the position N-3 of the cation and different alkyl substituents in the position N-1. Also, extraction of selected organic dyes was performed to demonstrate application of studied ionic liquids as novel extractants. (C) 2016 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights reserved.
T2  - Journal of Industrial and Engineering Chemistry
T1  - Aqueous biphasic system formation using 1-alkyl-3-ethylimidazolium bromide ionic liquids as new extractants
VL  - 40
SP  - 152
EP  - 160
DO  - 10.1016/j.jiec.2016.06.017
ER  - 

@article{
author = "Dimitrijević, Aleksandra and Zec, Nebojša and Zdolšek, Nikola and Dožić, Sanja and Tot, Aleksandar and Gadžurić, Slobodan and Vraneš, Milan and Trtić-Petrović, Tatjana M.",
year = "2016",
abstract = "In this work three 1-alkyl-3-ethylimidazolium bromide ionic liquids (alkyl = ethyl, hexyl and octyl) were synthesized applying both, conventional and microwave assisted synthetic paths. The phase diagrams for aqueous solutions of 1-alkyl-3-ethylimidazolium bromide ionic liquids as novel extractants combined with phosphate-based salts are reported and discussed in terms of aqueous biphasic system (ABS) formation. Merchuk equation was applied in order to correlate the,experimental binodal data. The liquid-liquid equilibrium data (tie-line compositions and tie-line length) were also experimentally determined by a gravimetric method. The influence of the alkyl chain length on ABS formation ability was investigated. It was found that ability to form ABS increases with the increase of the alkyl chain length on the imidazolium cation. Also, it was found that ionic liquids with ethyl group in the N-3 position better form ABS compared to those with methyl substituent. This was discussed in terms of increasing ionic liquid hydrophobicity and poor affinity for water. In order to better understand the impact of the alkyl side chain of the imidazolium ion and the efficiency of ABS formation, computer simulations were performed using investigated ionic liquids with the ethyl group in the position N-3 of the cation and different alkyl substituents in the position N-1. Also, extraction of selected organic dyes was performed to demonstrate application of studied ionic liquids as novel extractants. (C) 2016 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights reserved.",
journal = "Journal of Industrial and Engineering Chemistry",
title = "Aqueous biphasic system formation using 1-alkyl-3-ethylimidazolium bromide ionic liquids as new extractants",
volume = "40",
pages = "152-160",
doi = "10.1016/j.jiec.2016.06.017"
}

Dimitrijević, A., Zec, N., Zdolšek, N., Dožić, S., Tot, A., Gadžurić, S., Vraneš, M.,& Trtić-Petrović, T. M.. (2016). Aqueous biphasic system formation using 1-alkyl-3-ethylimidazolium bromide ionic liquids as new extractants. in Journal of Industrial and Engineering Chemistry, 40, 152-160.
https://doi.org/10.1016/j.jiec.2016.06.017

Dimitrijević A, Zec N, Zdolšek N, Dožić S, Tot A, Gadžurić S, Vraneš M, Trtić-Petrović TM. Aqueous biphasic system formation using 1-alkyl-3-ethylimidazolium bromide ionic liquids as new extractants. in Journal of Industrial and Engineering Chemistry. 2016;40:152-160.
doi:10.1016/j.jiec.2016.06.017 .

Dimitrijević, Aleksandra, Zec, Nebojša, Zdolšek, Nikola, Dožić, Sanja, Tot, Aleksandar, Gadžurić, Slobodan, Vraneš, Milan, Trtić-Petrović, Tatjana M., "Aqueous biphasic system formation using 1-alkyl-3-ethylimidazolium bromide ionic liquids as new extractants" in Journal of Industrial and Engineering Chemistry, 40 (2016):152-160,
https://doi.org/10.1016/j.jiec.2016.06.017 . .

TY  - JOUR
AU  - Babić, Dragan
AU  - Nikolic, R
AU  - Gadžurić, Slobodan
AU  - Zsigrai, Istvan J.
PY  - 2001
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/2505
AB  - Specific conductivity of molten mixtures of acetamide with following acetate salts was measured at 83 +/- 0.1degreesC : a) acetamide - anhydrous sodium acetate (up to 0.051 mole fraction), b) acetainide sodium acetate trihydrate (entire concentration range) and c) acetamide - zinc acetate dihydrate ( up to 0.24 mole fraction). Selected composition of all three mixtures, with low melting points were chosen for the studies of the changes of conductance with temperature. The mixtures: with sodium acetate both anhydrous and hydrated showed fairly high specific conductivity (approximate to10(-2) S/cm), nearly two orders of magnitude higher than the mixture with hydrated zinc acetate. Molar conductivity was also calculated. The results were discussed in terms of acetamide-salt-water interactions. Attempts were made to calculate the degree of dissociation of the salts in molten acetamide. The results were compared with the data obtained from earlier thermochemical studies of the same melt systems.
T2  - High Temperature Material Processes
T1  - Electrical conductivity of the acetamide-acetate salt melts
VL  - 5
IS  - 4
SP  - 595
EP  - 602
UR  - https://hdl.handle.net/21.15107/rcub_vinar_2505
ER  - 

@article{
author = "Babić, Dragan and Nikolic, R and Gadžurić, Slobodan and Zsigrai, Istvan J.",
year = "2001",
abstract = "Specific conductivity of molten mixtures of acetamide with following acetate salts was measured at 83 +/- 0.1degreesC : a) acetamide - anhydrous sodium acetate (up to 0.051 mole fraction), b) acetainide sodium acetate trihydrate (entire concentration range) and c) acetamide - zinc acetate dihydrate ( up to 0.24 mole fraction). Selected composition of all three mixtures, with low melting points were chosen for the studies of the changes of conductance with temperature. The mixtures: with sodium acetate both anhydrous and hydrated showed fairly high specific conductivity (approximate to10(-2) S/cm), nearly two orders of magnitude higher than the mixture with hydrated zinc acetate. Molar conductivity was also calculated. The results were discussed in terms of acetamide-salt-water interactions. Attempts were made to calculate the degree of dissociation of the salts in molten acetamide. The results were compared with the data obtained from earlier thermochemical studies of the same melt systems.",
journal = "High Temperature Material Processes",
title = "Electrical conductivity of the acetamide-acetate salt melts",
volume = "5",
number = "4",
pages = "595-602",
url = "https://hdl.handle.net/21.15107/rcub_vinar_2505"
}

Babić, D., Nikolic, R., Gadžurić, S.,& Zsigrai, I. J.. (2001). Electrical conductivity of the acetamide-acetate salt melts. in High Temperature Material Processes, 5(4), 595-602.
https://hdl.handle.net/21.15107/rcub_vinar_2505

Babić D, Nikolic R, Gadžurić S, Zsigrai IJ. Electrical conductivity of the acetamide-acetate salt melts. in High Temperature Material Processes. 2001;5(4):595-602.
https://hdl.handle.net/21.15107/rcub_vinar_2505 .

Babić, Dragan, Nikolic, R, Gadžurić, Slobodan, Zsigrai, Istvan J., "Electrical conductivity of the acetamide-acetate salt melts" in High Temperature Material Processes, 5, no. 4 (2001):595-602,
https://hdl.handle.net/21.15107/rcub_vinar_2505 .

TY  - JOUR
AU  - Zsigrai, Istvan J.
AU  - Gadžurić, Slobodan
AU  - Nikolic, R
PY  - 2001
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/2504
AB  - In this work a series of spectrophotometric measurements of cobalt(II) chloride in calcium nitrate tetrahydrate melts containing variable amounts of calcium chloride (from 0 to 3.1 mol dm(-3)) were performed at different temperatures from 40 to 70 degreesC. The solutions in pure calcium nitrate tetrahydrate showed octahedral co-ordination, the position of the absorption maximum being at 19420 cm(-1) (512 nm). Addition of chloride caused a shift of the absorption maximum toward lower energies and a large increase of the absorption coefficient indicating a change from octahedral to tetrahedral or distorted octahedral co-ordination, characteristic for cobalt(II) chloride complexes in aqueous nitrate melts. The position of the absorption maximum of the octahedral and tetrahedral complexes and the values of the molar absorption coefficients indicates some co-ordination also by nitrate ion. Stability constants for [CO(NO3)(4)](2-), [CO(NO3)(2)Cl-2](2-) and [COCl4](2-) and the corresponding resolved species spectra are reported.
T2  - High Temperature Material Processes
T1  - Cobalt(II) chloride complexes in calcium nitrate tetrahydrate melt
VL  - 5
IS  - 4
SP  - 573
EP  - 581
UR  - https://hdl.handle.net/21.15107/rcub_vinar_2504
ER  - 

@article{
author = "Zsigrai, Istvan J. and Gadžurić, Slobodan and Nikolic, R",
year = "2001",
abstract = "In this work a series of spectrophotometric measurements of cobalt(II) chloride in calcium nitrate tetrahydrate melts containing variable amounts of calcium chloride (from 0 to 3.1 mol dm(-3)) were performed at different temperatures from 40 to 70 degreesC. The solutions in pure calcium nitrate tetrahydrate showed octahedral co-ordination, the position of the absorption maximum being at 19420 cm(-1) (512 nm). Addition of chloride caused a shift of the absorption maximum toward lower energies and a large increase of the absorption coefficient indicating a change from octahedral to tetrahedral or distorted octahedral co-ordination, characteristic for cobalt(II) chloride complexes in aqueous nitrate melts. The position of the absorption maximum of the octahedral and tetrahedral complexes and the values of the molar absorption coefficients indicates some co-ordination also by nitrate ion. Stability constants for [CO(NO3)(4)](2-), [CO(NO3)(2)Cl-2](2-) and [COCl4](2-) and the corresponding resolved species spectra are reported.",
journal = "High Temperature Material Processes",
title = "Cobalt(II) chloride complexes in calcium nitrate tetrahydrate melt",
volume = "5",
number = "4",
pages = "573-581",
url = "https://hdl.handle.net/21.15107/rcub_vinar_2504"
}

Zsigrai, I. J., Gadžurić, S.,& Nikolic, R.. (2001). Cobalt(II) chloride complexes in calcium nitrate tetrahydrate melt. in High Temperature Material Processes, 5(4), 573-581.
https://hdl.handle.net/21.15107/rcub_vinar_2504

Zsigrai IJ, Gadžurić S, Nikolic R. Cobalt(II) chloride complexes in calcium nitrate tetrahydrate melt. in High Temperature Material Processes. 2001;5(4):573-581.
https://hdl.handle.net/21.15107/rcub_vinar_2504 .

Zsigrai, Istvan J., Gadžurić, Slobodan, Nikolic, R, "Cobalt(II) chloride complexes in calcium nitrate tetrahydrate melt" in High Temperature Material Processes, 5, no. 4 (2001):573-581,
https://hdl.handle.net/21.15107/rcub_vinar_2504 .

TY  - JOUR
AU  - Gadžurić, Slobodan
AU  - Zsigrai, Istvan J.
AU  - Nikolic, RM
PY  - 2001
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/2498
AB  - The complex formation between lead(II) ions and chloride and bromide ions in melts of Ca(NO3)(2 .) 4H(2)O . aCH(3)CONH(2) has been studied at different temperatures between 30 and 70 C. The formation constants of the complexes PbX+ and PbX2 (X = Cl, Br) were determined from emf measurements by means of Ag/AgX electrodes. The dependence of the formation constants for PbCl+ on the solvent melt composition has been analysed. The thermodynamic parameters DeltaH(11)(0) and DeltaS(11)(0) for PbX+ complex formation have been estimated. The parameters are compared with the literature data for the same process in dilute aqueous solutions and in some hydrated and anhydrous salt melts.
T2  - Zeitschrift fur Naturforschung. Section A: Journal of Physical Sciences
T1  - Thermodynamics of lead(II) halide complex formation in calcium nitrate tetrahydrate - Acetamide melts
VL  - 56
IS  - 12
SP  - 832
EP  - 836
UR  - https://hdl.handle.net/21.15107/rcub_vinar_2498
ER  - 

@article{
author = "Gadžurić, Slobodan and Zsigrai, Istvan J. and Nikolic, RM",
year = "2001",
abstract = "The complex formation between lead(II) ions and chloride and bromide ions in melts of Ca(NO3)(2 .) 4H(2)O . aCH(3)CONH(2) has been studied at different temperatures between 30 and 70 C. The formation constants of the complexes PbX+ and PbX2 (X = Cl, Br) were determined from emf measurements by means of Ag/AgX electrodes. The dependence of the formation constants for PbCl+ on the solvent melt composition has been analysed. The thermodynamic parameters DeltaH(11)(0) and DeltaS(11)(0) for PbX+ complex formation have been estimated. The parameters are compared with the literature data for the same process in dilute aqueous solutions and in some hydrated and anhydrous salt melts.",
journal = "Zeitschrift fur Naturforschung. Section A: Journal of Physical Sciences",
title = "Thermodynamics of lead(II) halide complex formation in calcium nitrate tetrahydrate - Acetamide melts",
volume = "56",
number = "12",
pages = "832-836",
url = "https://hdl.handle.net/21.15107/rcub_vinar_2498"
}

Gadžurić, S., Zsigrai, I. J.,& Nikolic, R.. (2001). Thermodynamics of lead(II) halide complex formation in calcium nitrate tetrahydrate - Acetamide melts. in Zeitschrift fur Naturforschung. Section A: Journal of Physical Sciences, 56(12), 832-836.
https://hdl.handle.net/21.15107/rcub_vinar_2498

Gadžurić S, Zsigrai IJ, Nikolic R. Thermodynamics of lead(II) halide complex formation in calcium nitrate tetrahydrate - Acetamide melts. in Zeitschrift fur Naturforschung. Section A: Journal of Physical Sciences. 2001;56(12):832-836.
https://hdl.handle.net/21.15107/rcub_vinar_2498 .

Gadžurić, Slobodan, Zsigrai, Istvan J., Nikolic, RM, "Thermodynamics of lead(II) halide complex formation in calcium nitrate tetrahydrate - Acetamide melts" in Zeitschrift fur Naturforschung. Section A: Journal of Physical Sciences, 56, no. 12 (2001):832-836,
https://hdl.handle.net/21.15107/rcub_vinar_2498 .

TY  - JOUR
AU  - Zsigrai, Istvan J.
AU  - Gadžurić, Slobodan
AU  - Nikolic, RM
PY  - 2001
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/2412
AB  - The complex formation between cadmium(II) ions and chloride and bromide ions in the melt of 0.8CH(3)CONH(2)-0.2Ca(NO3)(2). 4H(2)O has been studied at six temperatures between 30 and 80 degreesC. The formation constants of the complexes CdX+ and CdX2 (X=CI, Br) were determined from Emf measurements by means of Ag/AgX electrodes. The thermodynamic parameters DeltaH(mn)degrees and DeltaS(mn)degrees for the stepwise complex formation [GRAPHICS] have been estimated. The results are DeltaH(11)degrees = 4.2 kJ mol(-1). DeltaS(11)degrees = 52.4 J K-1 mol(-1), DeltaH(12)degrees = 3.3 kJ mol(-1) DeltaS(12)degrees = 40.7 J K-1 mol(-1) for the chloride complexes and DeltaH(11)degrees = -3.3 kJ mol(-1), DeltaS(11)degrees = 33.0 J K-1 mol(-1), DeltaH(12)degrees = -2.5 kJ mol(-1), DeltaS(12)degrees = 30.4 J K-1 mol(-1) for the bromide complexes. The parameters are compared with the literature data for the same process in dilute aqueous solutions and in some hydrated salt melts.
T2  - Magyar Kemiai Folyoirat
T1  - Thermodynamics of cadmium halide complex formation in acetamide-calcium nitrate tetrahydrate melt
VL  - 107
IS  - 1
SP  - 36
EP  - 42
UR  - https://hdl.handle.net/21.15107/rcub_vinar_2412
ER  - 

@article{
author = "Zsigrai, Istvan J. and Gadžurić, Slobodan and Nikolic, RM",
year = "2001",
abstract = "The complex formation between cadmium(II) ions and chloride and bromide ions in the melt of 0.8CH(3)CONH(2)-0.2Ca(NO3)(2). 4H(2)O has been studied at six temperatures between 30 and 80 degreesC. The formation constants of the complexes CdX+ and CdX2 (X=CI, Br) were determined from Emf measurements by means of Ag/AgX electrodes. The thermodynamic parameters DeltaH(mn)degrees and DeltaS(mn)degrees for the stepwise complex formation [GRAPHICS] have been estimated. The results are DeltaH(11)degrees = 4.2 kJ mol(-1). DeltaS(11)degrees = 52.4 J K-1 mol(-1), DeltaH(12)degrees = 3.3 kJ mol(-1) DeltaS(12)degrees = 40.7 J K-1 mol(-1) for the chloride complexes and DeltaH(11)degrees = -3.3 kJ mol(-1), DeltaS(11)degrees = 33.0 J K-1 mol(-1), DeltaH(12)degrees = -2.5 kJ mol(-1), DeltaS(12)degrees = 30.4 J K-1 mol(-1) for the bromide complexes. The parameters are compared with the literature data for the same process in dilute aqueous solutions and in some hydrated salt melts.",
journal = "Magyar Kemiai Folyoirat",
title = "Thermodynamics of cadmium halide complex formation in acetamide-calcium nitrate tetrahydrate melt",
volume = "107",
number = "1",
pages = "36-42",
url = "https://hdl.handle.net/21.15107/rcub_vinar_2412"
}

Zsigrai, I. J., Gadžurić, S.,& Nikolic, R.. (2001). Thermodynamics of cadmium halide complex formation in acetamide-calcium nitrate tetrahydrate melt. in Magyar Kemiai Folyoirat, 107(1), 36-42.
https://hdl.handle.net/21.15107/rcub_vinar_2412

Zsigrai IJ, Gadžurić S, Nikolic R. Thermodynamics of cadmium halide complex formation in acetamide-calcium nitrate tetrahydrate melt. in Magyar Kemiai Folyoirat. 2001;107(1):36-42.
https://hdl.handle.net/21.15107/rcub_vinar_2412 .

Zsigrai, Istvan J., Gadžurić, Slobodan, Nikolic, RM, "Thermodynamics of cadmium halide complex formation in acetamide-calcium nitrate tetrahydrate melt" in Magyar Kemiai Folyoirat, 107, no. 1 (2001):36-42,
https://hdl.handle.net/21.15107/rcub_vinar_2412 .

TY  - JOUR
AU  - Gadžurić, Slobodan
AU  - Zsigrai, Istvan J.
AU  - Nikolic, RM
PY  - 1999
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/2297
AB  - The complex formation between cadmium(II) ions and chloride and bromide ions in the melt of 0.8CH(3)CONH(2)-0.2Ca(NO3)(2). 4H(2)O has been studied at six temperatures between 30 and 80 degrees C. The formation constants of the complexes CdX+ and CdX2 (X-Cl Br) were determined from emf measurements by means of Ag/AgX electrodes. The thermodynamic parameters Delta H(mn)degrees, and Delta S(mn)degrees, for the stepwise complex formation CdmXn-12m-n + X(-)reversible arrow CdmXn2m-n have been estimated. The results are Delta H(11)degrees = 4.2 kJ mol(-1), Delta S(11)degrees = 52.4 J K-1 mol(-1), Delta H(12)degrees = 3.3 kJ mol(-1), Delta S(12)degrees = 40.7 J K-1 mol(-1) for the chloride complexes and Delta H(11)degrees = -3.3 kJ mol(-1), Delta S(11)degrees -33.0 J K-1 mol(-1), Delta H(12)degrees = -2.5 kJ mol(-1), Delta S(12)degrees = 30.4 J K-1 mol(-1) for the bromide complexes. The parameters are compared with the literature data for the same process in dilute aqueous solutions and in some hydrated salt melts. (C) 1999 Elsevier Science B.V. All rights reserved.
T2  - Journal of Molecular Liquids
T1  - Thermodynamics of cadmium halide complex formation in acetamide - Calcium nitrate tetrahydrate melt
VL  - 83
IS  - 1-3
SP  - 75
EP  - 82
DO  - 10.1016/S0167-7322(99)00074-4
ER  - 

@article{
author = "Gadžurić, Slobodan and Zsigrai, Istvan J. and Nikolic, RM",
year = "1999",
abstract = "The complex formation between cadmium(II) ions and chloride and bromide ions in the melt of 0.8CH(3)CONH(2)-0.2Ca(NO3)(2). 4H(2)O has been studied at six temperatures between 30 and 80 degrees C. The formation constants of the complexes CdX+ and CdX2 (X-Cl Br) were determined from emf measurements by means of Ag/AgX electrodes. The thermodynamic parameters Delta H(mn)degrees, and Delta S(mn)degrees, for the stepwise complex formation CdmXn-12m-n + X(-)reversible arrow CdmXn2m-n have been estimated. The results are Delta H(11)degrees = 4.2 kJ mol(-1), Delta S(11)degrees = 52.4 J K-1 mol(-1), Delta H(12)degrees = 3.3 kJ mol(-1), Delta S(12)degrees = 40.7 J K-1 mol(-1) for the chloride complexes and Delta H(11)degrees = -3.3 kJ mol(-1), Delta S(11)degrees -33.0 J K-1 mol(-1), Delta H(12)degrees = -2.5 kJ mol(-1), Delta S(12)degrees = 30.4 J K-1 mol(-1) for the bromide complexes. The parameters are compared with the literature data for the same process in dilute aqueous solutions and in some hydrated salt melts. (C) 1999 Elsevier Science B.V. All rights reserved.",
journal = "Journal of Molecular Liquids",
title = "Thermodynamics of cadmium halide complex formation in acetamide - Calcium nitrate tetrahydrate melt",
volume = "83",
number = "1-3",
pages = "75-82",
doi = "10.1016/S0167-7322(99)00074-4"
}

Gadžurić, S., Zsigrai, I. J.,& Nikolic, R.. (1999). Thermodynamics of cadmium halide complex formation in acetamide - Calcium nitrate tetrahydrate melt. in Journal of Molecular Liquids, 83(1-3), 75-82.
https://doi.org/10.1016/S0167-7322(99)00074-4

Gadžurić S, Zsigrai IJ, Nikolic R. Thermodynamics of cadmium halide complex formation in acetamide - Calcium nitrate tetrahydrate melt. in Journal of Molecular Liquids. 1999;83(1-3):75-82.
doi:10.1016/S0167-7322(99)00074-4 .

Gadžurić, Slobodan, Zsigrai, Istvan J., Nikolic, RM, "Thermodynamics of cadmium halide complex formation in acetamide - Calcium nitrate tetrahydrate melt" in Journal of Molecular Liquids, 83, no. 1-3 (1999):75-82,
https://doi.org/10.1016/S0167-7322(99)00074-4 . .

TY  - JOUR
AU  - Marinković, Miloš
AU  - Nikolić, Ružica M.
AU  - Savović, Jelena
AU  - Gadžurić, Slobodan
AU  - Zsigrai, Istvan J.
PY  - 1998
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/2119
AB  - The possibility to combine two physico-chemical phenomena is studied in this work in order to attain simultaneous control of temperature and light intensity in a greenhouse: (a) isothermal heat storage in phase change materials and (b) thermochromic behavior of complex compounds dissolved in the phase change materials. Two binary mixtures melting near the ambient temperature were studied: (a) 0.925 Ca(NO3)(2) . 4.06 H2O + 0.075 CaCl2 . 6.11 H2O melting at 35.6 degrees C and (b) 0.9 CH3CONH2 + 0.1 Ca(NO3)(2) . 4 H2O, melting at 27.7 degrees C. The melting temperature, the enthalpy of fusion and the heat capacity of both mixtures were determined from DSC measurements. Both mixtures showed to be suitable solvents for the formation of consecutive cobalt(II) chloride complexes. The compositions of the complex compounds were adjusted in each mixture so that the absorption spectra in visible spectral range exhibited low absorbance at the melting temperature and a pronounced increase of the absorbance and/or change of color with the increase of temperature in the range relevant for passive solar energy receivers. The combined latent heat storage and the outstanding reversible change of the optical properties of the dissolved complex compounds with temperature is proposed to be applied in solar heated agricultural greenhouses in areas with fluctuating climate conditions. The increase of absorbance with temperature acts as an auto-regulated shading protection from overheating. (C) 1998 Elsevier Science B.V. All rights reserved.
T2  - Solar Energy Materials and Solar Cells
T1  - Thermochromic complex compounds in phase change materials: Possible application in an agricultural greenhouse
VL  - 51
IS  - 3-4
SP  - 401
EP  - 411
DO  - 10.1016/S0927-0248(97)00259-6
ER  - 

@article{
author = "Marinković, Miloš and Nikolić, Ružica M. and Savović, Jelena and Gadžurić, Slobodan and Zsigrai, Istvan J.",
year = "1998",
abstract = "The possibility to combine two physico-chemical phenomena is studied in this work in order to attain simultaneous control of temperature and light intensity in a greenhouse: (a) isothermal heat storage in phase change materials and (b) thermochromic behavior of complex compounds dissolved in the phase change materials. Two binary mixtures melting near the ambient temperature were studied: (a) 0.925 Ca(NO3)(2) . 4.06 H2O + 0.075 CaCl2 . 6.11 H2O melting at 35.6 degrees C and (b) 0.9 CH3CONH2 + 0.1 Ca(NO3)(2) . 4 H2O, melting at 27.7 degrees C. The melting temperature, the enthalpy of fusion and the heat capacity of both mixtures were determined from DSC measurements. Both mixtures showed to be suitable solvents for the formation of consecutive cobalt(II) chloride complexes. The compositions of the complex compounds were adjusted in each mixture so that the absorption spectra in visible spectral range exhibited low absorbance at the melting temperature and a pronounced increase of the absorbance and/or change of color with the increase of temperature in the range relevant for passive solar energy receivers. The combined latent heat storage and the outstanding reversible change of the optical properties of the dissolved complex compounds with temperature is proposed to be applied in solar heated agricultural greenhouses in areas with fluctuating climate conditions. The increase of absorbance with temperature acts as an auto-regulated shading protection from overheating. (C) 1998 Elsevier Science B.V. All rights reserved.",
journal = "Solar Energy Materials and Solar Cells",
title = "Thermochromic complex compounds in phase change materials: Possible application in an agricultural greenhouse",
volume = "51",
number = "3-4",
pages = "401-411",
doi = "10.1016/S0927-0248(97)00259-6"
}

Marinković, M., Nikolić, R. M., Savović, J., Gadžurić, S.,& Zsigrai, I. J.. (1998). Thermochromic complex compounds in phase change materials: Possible application in an agricultural greenhouse. in Solar Energy Materials and Solar Cells, 51(3-4), 401-411.
https://doi.org/10.1016/S0927-0248(97)00259-6

Marinković M, Nikolić RM, Savović J, Gadžurić S, Zsigrai IJ. Thermochromic complex compounds in phase change materials: Possible application in an agricultural greenhouse. in Solar Energy Materials and Solar Cells. 1998;51(3-4):401-411.
doi:10.1016/S0927-0248(97)00259-6 .

Marinković, Miloš, Nikolić, Ružica M., Savović, Jelena, Gadžurić, Slobodan, Zsigrai, Istvan J., "Thermochromic complex compounds in phase change materials: Possible application in an agricultural greenhouse" in Solar Energy Materials and Solar Cells, 51, no. 3-4 (1998):401-411,
https://doi.org/10.1016/S0927-0248(97)00259-6 . .