Zdolšek, Nikola

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Authority KeyName Variants
orcid::0000-0002-2665-0111
  • Zdolšek, Nikola (11)
Projects
Physics and Chemistry with Ion Beams Nanostructured Functional and Composite Materials in Catalytic and Sorption Processes
Lithium-ion batteries and fuel cells - research and development COST Action [CM1206]
Grant Agency of the Czech Republic [17-08218S] Sustainable and green chemistry approach for environmental friendly analytical methods and energy storage
Czech Science Foundation (17-08218S) (MB) ERDF through COMPETE - Programa Operacional Competitividade e Internacionalizacao (POCI) - POCI-01-0145-FEDER-006984
ERDF through COMPETE - Programa Operacional Competitividade e Internacionalizacao (POCI) [POCI-01-0145-FEDER-006984] FCT - Fundacao para a Ciencia e a Tecnologia
FCT - Fundacao para a Ciencia e a Tecnologia [SFRH/BD/95411/2013] FCT - SFRH/BD/95411/2013
Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200017 (University of Belgrade, Institute of Nuclear Sciences 'Vinča', Belgrade-Vinča) Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200146 (University of Belgrade, Faculty of Physical Chemistry)
Ministry of Education, Science and Technological Development of the Republic of Serbia Ministry of Education, Sports, and Youth of the Czech Republic - COST LD14090
Ministry of Education, Sports, and Youth of the Czech Republic [COST LD14090] Portuguese Foundation for Science and Technology [SFRH/BD/137470/2018, IST-ID/156/2018, UIDP/04540/2020]
Project "AIProc-Mat@N2020-Advanced Industrial Processes and Materials for a Sustainable Northern Region of Portugal 2020" - Norte Portugal Regional Operational Programme (NORTE 2020), under the Portugal 2020 Partnership Agreement, through the European Regional Development Fund (ERDF) (NORTE-01-0145-FEDER-000006) Project POCI-01-0145-FEDER-006984 - Associate Laboratory LSRE-LCM funded by ERDF through COMPETE2020-Programa Operacional Competitividade e Internacionalizacao (POCI)

Author's Bibliography

Ionic liquid-derived carbon-supported metal electrocatalysts as anodes in direct borohydride-peroxide fuel cells

Milikić, Jadranka; Oliveira, Raisa Costa Paes; Tapia, Andres; Santos, Diogo M.F.; Zdolšek, Nikola; Trtić-Petrović, Tatjana M.; Vraneš, Milan; Šljukić, Biljana

(2021)

TY  - JOUR
AU  - Milikić, Jadranka
AU  - Oliveira, Raisa Costa Paes
AU  - Tapia, Andres
AU  - Santos, Diogo M.F.
AU  - Zdolšek, Nikola
AU  - Trtić-Petrović, Tatjana M.
AU  - Vraneš, Milan
AU  - Šljukić, Biljana
PY  - 2021
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/9801
AB  - Three different carbon-supported metal (gold, platinum, nickel) nanoparticle (M/c-IL) electrocatalysts are prepared by template-free carbonization of the corresponding ionic liquids, namely [Hmim][AuCl4 ], [Hmim]2 [PtCl4 ], and [C16mim]2 [NiCl4 ], as confirmed by X-ray diffraction analysis, scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy and Raman spectroscopy. The electrochemical investigation of borohydride oxidation reaction (BOR) at the three electrocatalysts by cyclic voltammetry reveals different behavior for each material. BOR is found to be a first-order reaction at the three electrocatalysts, with an apparent activation energy of 10.6 and 13.8 kJ mol−1 for Pt/c-IL and Au/c-IL electrocatalysts, respectively. A number of exchanged electrons of 5.0, 2.4, and 2.0 is obtained for BOR at Pt/c-IL, Au/c-IL, and Ni/c-IL electrodes, respectively. Direct borohydride-peroxide fuel cell (DBPFC) tests done at temperatures in the 25–65◦C range show ca. four times higher power density when using a Pt/c-IL anode than with an Au/c-IL anode. Peak power densities of 40.6 and 120.5 mW cm−2 are achieved at 25 and 65◦C, respectively, for DBPFC with a Pt/c-IL anode electrocatalyst. © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/).
T2  - Catalysts
T1  - Ionic liquid-derived carbon-supported metal electrocatalysts as anodes in direct borohydride-peroxide fuel cells
VL  - 11
IS  - 5
DO  - 10.3390/catal11050632
ER  - 
@article{
author = "Milikić, Jadranka and Oliveira, Raisa Costa Paes and Tapia, Andres and Santos, Diogo M.F. and Zdolšek, Nikola and Trtić-Petrović, Tatjana M. and Vraneš, Milan and Šljukić, Biljana",
year = "2021",
abstract = "Three different carbon-supported metal (gold, platinum, nickel) nanoparticle (M/c-IL) electrocatalysts are prepared by template-free carbonization of the corresponding ionic liquids, namely [Hmim][AuCl4 ], [Hmim]2 [PtCl4 ], and [C16mim]2 [NiCl4 ], as confirmed by X-ray diffraction analysis, scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy and Raman spectroscopy. The electrochemical investigation of borohydride oxidation reaction (BOR) at the three electrocatalysts by cyclic voltammetry reveals different behavior for each material. BOR is found to be a first-order reaction at the three electrocatalysts, with an apparent activation energy of 10.6 and 13.8 kJ mol−1 for Pt/c-IL and Au/c-IL electrocatalysts, respectively. A number of exchanged electrons of 5.0, 2.4, and 2.0 is obtained for BOR at Pt/c-IL, Au/c-IL, and Ni/c-IL electrodes, respectively. Direct borohydride-peroxide fuel cell (DBPFC) tests done at temperatures in the 25–65◦C range show ca. four times higher power density when using a Pt/c-IL anode than with an Au/c-IL anode. Peak power densities of 40.6 and 120.5 mW cm−2 are achieved at 25 and 65◦C, respectively, for DBPFC with a Pt/c-IL anode electrocatalyst. © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/).",
journal = "Catalysts",
title = "Ionic liquid-derived carbon-supported metal electrocatalysts as anodes in direct borohydride-peroxide fuel cells",
volume = "11",
number = "5",
doi = "10.3390/catal11050632"
}
Milikić, J., Oliveira, R. C. P., Tapia, A., Santos, D. M.F., Zdolšek, N., Trtić-Petrović, T. M., Vraneš, M.,& Šljukić, B.. (2021). Ionic liquid-derived carbon-supported metal electrocatalysts as anodes in direct borohydride-peroxide fuel cells. in Catalysts, 11(5).
https://doi.org/10.3390/catal11050632
Milikić J, Oliveira RCP, Tapia A, Santos DM, Zdolšek N, Trtić-Petrović TM, Vraneš M, Šljukić B. Ionic liquid-derived carbon-supported metal electrocatalysts as anodes in direct borohydride-peroxide fuel cells. in Catalysts. 2021;11(5).
doi:10.3390/catal11050632 .
Milikić, Jadranka, Oliveira, Raisa Costa Paes, Tapia, Andres, Santos, Diogo M.F., Zdolšek, Nikola, Trtić-Petrović, Tatjana M., Vraneš, Milan, Šljukić, Biljana, "Ionic liquid-derived carbon-supported metal electrocatalysts as anodes in direct borohydride-peroxide fuel cells" in Catalysts, 11, no. 5 (2021),
https://doi.org/10.3390/catal11050632 . .

Heat capacity of 1-hexadecyl-3-methylimidazolium based ionic liquids in solid and liquid phase

Bendova, Magdalena; Wagner, Zdenek; Bogdanov, Milen G.; Čanji, Maja; Zdolšek, Nikola

(2020)

TY  - JOUR
AU  - Bendova, Magdalena
AU  - Wagner, Zdenek
AU  - Bogdanov, Milen G.
AU  - Čanji, Maja
AU  - Zdolšek, Nikola
PY  - 2020
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8859
AB  - In this work, two ionic liquids with a 1-hexadecyl-3-methylimidazolium cation were synthesized with different anions; chloride and saccharinate, respectively, both of them showing melting points above room temperature, ranging between (324.15 and 338.15) K and enthalpies of fusion close to or higher than 100 J/g, making them potentially suitable phase-change materials (PCMs) for latent heat storage. This application potential can be enhanced by a suitably large heat capacity and thermal conductivity of the material both in the liquid and solid phase. Heat capacity was therefore measured in this work as a function of temperature using the differential scanning calorimetry (DSC) to determine how it is affected by the anion structure. Care has been taken to evaluate the influence of the phase change on the measured data. The experimental data have then been analyzed by means of methods based on mathematical gnostics (MG). As a non-statistical approach towards data uncertainty, MG enabled us to analyze the underlying phenomena that affect the value of the experimental heat capacity. © 2020 Elsevier B.V.
T2  - Journal of Molecular Liquids
T1  - Heat capacity of 1-hexadecyl-3-methylimidazolium based ionic liquids in solid and liquid phase
VL  - 305
SP  - 112847
DO  - 10.1016/j.molliq.2020.112847
ER  - 
@article{
author = "Bendova, Magdalena and Wagner, Zdenek and Bogdanov, Milen G. and Čanji, Maja and Zdolšek, Nikola",
year = "2020",
abstract = "In this work, two ionic liquids with a 1-hexadecyl-3-methylimidazolium cation were synthesized with different anions; chloride and saccharinate, respectively, both of them showing melting points above room temperature, ranging between (324.15 and 338.15) K and enthalpies of fusion close to or higher than 100 J/g, making them potentially suitable phase-change materials (PCMs) for latent heat storage. This application potential can be enhanced by a suitably large heat capacity and thermal conductivity of the material both in the liquid and solid phase. Heat capacity was therefore measured in this work as a function of temperature using the differential scanning calorimetry (DSC) to determine how it is affected by the anion structure. Care has been taken to evaluate the influence of the phase change on the measured data. The experimental data have then been analyzed by means of methods based on mathematical gnostics (MG). As a non-statistical approach towards data uncertainty, MG enabled us to analyze the underlying phenomena that affect the value of the experimental heat capacity. © 2020 Elsevier B.V.",
journal = "Journal of Molecular Liquids",
title = "Heat capacity of 1-hexadecyl-3-methylimidazolium based ionic liquids in solid and liquid phase",
volume = "305",
pages = "112847",
doi = "10.1016/j.molliq.2020.112847"
}
Bendova, M., Wagner, Z., Bogdanov, M. G., Čanji, M.,& Zdolšek, N.. (2020). Heat capacity of 1-hexadecyl-3-methylimidazolium based ionic liquids in solid and liquid phase. in Journal of Molecular Liquids, 305, 112847.
https://doi.org/10.1016/j.molliq.2020.112847
Bendova M, Wagner Z, Bogdanov MG, Čanji M, Zdolšek N. Heat capacity of 1-hexadecyl-3-methylimidazolium based ionic liquids in solid and liquid phase. in Journal of Molecular Liquids. 2020;305:112847.
doi:10.1016/j.molliq.2020.112847 .
Bendova, Magdalena, Wagner, Zdenek, Bogdanov, Milen G., Čanji, Maja, Zdolšek, Nikola, "Heat capacity of 1-hexadecyl-3-methylimidazolium based ionic liquids in solid and liquid phase" in Journal of Molecular Liquids, 305 (2020):112847,
https://doi.org/10.1016/j.molliq.2020.112847 . .
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Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: pseudocapacitance versus electrical double layer

Zdolšek, Nikola; Rocha, Raquel P.; Krstić, Jugoslav B.; Trtić-Petrović, Tatjana M.; Šljukić, Biljana; Figueiredo, Jose L.; Vujković, Milica

(2019)

TY  - JOUR
AU  - Zdolšek, Nikola
AU  - Rocha, Raquel P.
AU  - Krstić, Jugoslav B.
AU  - Trtić-Petrović, Tatjana M.
AU  - Šljukić, Biljana
AU  - Figueiredo, Jose L.
AU  - Vujković, Milica
PY  - 2019
UR  - https://linkinghub.elsevier.com/retrieve/pii/S0013468618328482
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8023
AB  - This work shows the potential application of carbon materials prepared by three different ionic liquid-based methods, using 1-butyl-3-methylimidazolium methanesulfonate [bmim][MeSO3], for electrochemical supercapacitors. The effects of [bmim][MeSO3] on morphology, texture and surface chemistry of prepared materials has been explored by SEM/TEM, N2/CO2 adsorption measurements and XPS. The results indicate the possibility of synthesis of carbon materials with tunable physicochemical properties using ionic liquid based methods. The charge storage behavior of all materials was studied in three different pH aqueous electrolytes. The pseudocapacitive and double layer contributions were estimated and discussed from the aspect of the textural changes and the changes of the chemical composition of surface functional groups containing heteroatoms. C[dbnd]O type functional groups, with the contribution of COOH groups, were found to be responsible for a different amount of charge, which could be stored in alkaline and acidic electrolytic solution. The material prepared by direct carbonization of [bmim][MeSO3], showed the best electrochemical performance in alkaline electrolyte with a capacitance of 187 F g−1 at 5 mV s−1 (or 148 F g−1 at 1 A g−1), due to the contribution of both electric-double layer capacitance and pseudocapacitance which arises from oxygen, nitrogen and sulfur functional groups. © 2018 Elsevier Ltd
T2  - Electrochimica Acta
T1  - Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: pseudocapacitance versus electrical double layer
VL  - 298
SP  - 541
EP  - 551
DO  - 10.1016/j.electacta.2018.12.129
ER  - 
@article{
author = "Zdolšek, Nikola and Rocha, Raquel P. and Krstić, Jugoslav B. and Trtić-Petrović, Tatjana M. and Šljukić, Biljana and Figueiredo, Jose L. and Vujković, Milica",
year = "2019",
abstract = "This work shows the potential application of carbon materials prepared by three different ionic liquid-based methods, using 1-butyl-3-methylimidazolium methanesulfonate [bmim][MeSO3], for electrochemical supercapacitors. The effects of [bmim][MeSO3] on morphology, texture and surface chemistry of prepared materials has been explored by SEM/TEM, N2/CO2 adsorption measurements and XPS. The results indicate the possibility of synthesis of carbon materials with tunable physicochemical properties using ionic liquid based methods. The charge storage behavior of all materials was studied in three different pH aqueous electrolytes. The pseudocapacitive and double layer contributions were estimated and discussed from the aspect of the textural changes and the changes of the chemical composition of surface functional groups containing heteroatoms. C[dbnd]O type functional groups, with the contribution of COOH groups, were found to be responsible for a different amount of charge, which could be stored in alkaline and acidic electrolytic solution. The material prepared by direct carbonization of [bmim][MeSO3], showed the best electrochemical performance in alkaline electrolyte with a capacitance of 187 F g−1 at 5 mV s−1 (or 148 F g−1 at 1 A g−1), due to the contribution of both electric-double layer capacitance and pseudocapacitance which arises from oxygen, nitrogen and sulfur functional groups. © 2018 Elsevier Ltd",
journal = "Electrochimica Acta",
title = "Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: pseudocapacitance versus electrical double layer",
volume = "298",
pages = "541-551",
doi = "10.1016/j.electacta.2018.12.129"
}
Zdolšek, N., Rocha, R. P., Krstić, J. B., Trtić-Petrović, T. M., Šljukić, B., Figueiredo, J. L.,& Vujković, M.. (2019). Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: pseudocapacitance versus electrical double layer. in Electrochimica Acta, 298, 541-551.
https://doi.org/10.1016/j.electacta.2018.12.129
Zdolšek N, Rocha RP, Krstić JB, Trtić-Petrović TM, Šljukić B, Figueiredo JL, Vujković M. Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: pseudocapacitance versus electrical double layer. in Electrochimica Acta. 2019;298:541-551.
doi:10.1016/j.electacta.2018.12.129 .
Zdolšek, Nikola, Rocha, Raquel P., Krstić, Jugoslav B., Trtić-Petrović, Tatjana M., Šljukić, Biljana, Figueiredo, Jose L., Vujković, Milica, "Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: pseudocapacitance versus electrical double layer" in Electrochimica Acta, 298 (2019):541-551,
https://doi.org/10.1016/j.electacta.2018.12.129 . .
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16
17

Corrigendum to “Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: Pseudocapacitance versus electrical double layer” [Electrochim. Acta 298 (2019) 541–551]

Zdolšek, Nikola; Rocha, Raquel P.; Krstić, Jugoslav B.; Trtić-Petrović, Tatjana M.; Šljukić, Biljana; Figueiredo, José L.; Vujković, Milica

(2019)

TY  - JOUR
AU  - Zdolšek, Nikola
AU  - Rocha, Raquel P.
AU  - Krstić, Jugoslav B.
AU  - Trtić-Petrović, Tatjana M.
AU  - Šljukić, Biljana
AU  - Figueiredo, José L.
AU  - Vujković, Milica
PY  - 2019
UR  - https://linkinghub.elsevier.com/retrieve/pii/S0013468619307960
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8159
AB  - The authors regret errors in the above mentioned article in the equation (2)as well as in the Fig. 10a. In the equation (2)the number 2 was accidently omitted, whereas the values for the x-axis of Fig. 10a were doubled by accident. The authors would like to apologise for any inconvenience caused. The corrected equation (2)and Fig. 10 are shown below. [Formula presented][Figure presented]Fig. 10. a)Galvanostatic charge-discharge curves for Carb-IL at different current densities in 6 M KOH and b)dependence of the discharge specific capacitance of Carb-IL on the number of cycles, at 5 A g −1 . © 2018 Elsevier Ltd
T2  - Electrochimica Acta
T1  - Corrigendum to “Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: Pseudocapacitance versus electrical double layer” [Electrochim. Acta 298 (2019) 541–551]
VL  - 310
SP  - 221
DO  - 10.1016/j.electacta.2019.04.108
ER  - 
@article{
author = "Zdolšek, Nikola and Rocha, Raquel P. and Krstić, Jugoslav B. and Trtić-Petrović, Tatjana M. and Šljukić, Biljana and Figueiredo, José L. and Vujković, Milica",
year = "2019",
abstract = "The authors regret errors in the above mentioned article in the equation (2)as well as in the Fig. 10a. In the equation (2)the number 2 was accidently omitted, whereas the values for the x-axis of Fig. 10a were doubled by accident. The authors would like to apologise for any inconvenience caused. The corrected equation (2)and Fig. 10 are shown below. [Formula presented][Figure presented]Fig. 10. a)Galvanostatic charge-discharge curves for Carb-IL at different current densities in 6 M KOH and b)dependence of the discharge specific capacitance of Carb-IL on the number of cycles, at 5 A g −1 . © 2018 Elsevier Ltd",
journal = "Electrochimica Acta",
title = "Corrigendum to “Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: Pseudocapacitance versus electrical double layer” [Electrochim. Acta 298 (2019) 541–551]",
volume = "310",
pages = "221",
doi = "10.1016/j.electacta.2019.04.108"
}
Zdolšek, N., Rocha, R. P., Krstić, J. B., Trtić-Petrović, T. M., Šljukić, B., Figueiredo, J. L.,& Vujković, M.. (2019). Corrigendum to “Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: Pseudocapacitance versus electrical double layer” [Electrochim. Acta 298 (2019) 541–551]. in Electrochimica Acta, 310, 221.
https://doi.org/10.1016/j.electacta.2019.04.108
Zdolšek N, Rocha RP, Krstić JB, Trtić-Petrović TM, Šljukić B, Figueiredo JL, Vujković M. Corrigendum to “Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: Pseudocapacitance versus electrical double layer” [Electrochim. Acta 298 (2019) 541–551]. in Electrochimica Acta. 2019;310:221.
doi:10.1016/j.electacta.2019.04.108 .
Zdolšek, Nikola, Rocha, Raquel P., Krstić, Jugoslav B., Trtić-Petrović, Tatjana M., Šljukić, Biljana, Figueiredo, José L., Vujković, Milica, "Corrigendum to “Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: Pseudocapacitance versus electrical double layer” [Electrochim. Acta 298 (2019) 541–551]" in Electrochimica Acta, 310 (2019):221,
https://doi.org/10.1016/j.electacta.2019.04.108 . .

Phase transitions in higher-melting imidazolium-based ionic liquids: Experiments and advanced data analysis

Čanji, Maja; Bendova, Magdalena; Bogdanov, Milen G.; Wagner, Zdenek; Zdolšek, Nikola; Quirion, François; Jandová, Věra; Vrbka, Pavel

(2019)

TY  - JOUR
AU  - Čanji, Maja
AU  - Bendova, Magdalena
AU  - Bogdanov, Milen G.
AU  - Wagner, Zdenek
AU  - Zdolšek, Nikola
AU  - Quirion, François
AU  - Jandová, Věra
AU  - Vrbka, Pavel
PY  - 2019
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8423
AB  - As thermal energy storage becomes an increasingly important topic, good knowledge of properties of phase-change materials (PCM) is essential. Among other properties, a good PCM should show a large enthalpy of melting, reproducible melting/solidification cycles, and long-term thermal stability. Temperatures and enthalpies of fusion should be determined at a possibly large range of conditions to allow for a critical evaluation of the experimental data and assessment of the material application potential. In this work, imidazolium-based ionic liquids (ILs) with long alkyl chain substituents 1-hexadecyl-3-methylimidazolium chloride and 1-hexadecyl-3-methyl-imidazolium saccharinate were studied in view of their possible use as phase-change materials. Differential scanning calorimetry (DSC) and the heat-leak modulus (HLM) methods were used to determine the temperatures and the enthalpies of phase transitions in the studied ILs, enabling us to study the influence of the heating and cooling rates on the measured properties. Enthalpies of fusion near to or larger than 100 J·g−1 were found in the studied ionic liquids, making them promising candidates for thermal energy storage. Peaks corresponding to possible liquid crystalline phases in the DSC traces of 1-hexadecyl-3-methylimidazolium saccharinate were observed, pointing to more complex phase behaviour of the studied ionic liquids. Finally, to critically evaluate the experimental data measured in this work, methods based on mathematical gnostics were used. Repeatability of measurements and the degree of mutual agreement between the methods used in this work could thus be determined. © 2019 Elsevier B.V.
T2  - Journal of Molecular Liquids
T1  - Phase transitions in higher-melting imidazolium-based ionic liquids: Experiments and advanced data analysis
VL  - 292
SP  - 111222
DO  - 10.1016/j.molliq.2019.111222
ER  - 
@article{
author = "Čanji, Maja and Bendova, Magdalena and Bogdanov, Milen G. and Wagner, Zdenek and Zdolšek, Nikola and Quirion, François and Jandová, Věra and Vrbka, Pavel",
year = "2019",
abstract = "As thermal energy storage becomes an increasingly important topic, good knowledge of properties of phase-change materials (PCM) is essential. Among other properties, a good PCM should show a large enthalpy of melting, reproducible melting/solidification cycles, and long-term thermal stability. Temperatures and enthalpies of fusion should be determined at a possibly large range of conditions to allow for a critical evaluation of the experimental data and assessment of the material application potential. In this work, imidazolium-based ionic liquids (ILs) with long alkyl chain substituents 1-hexadecyl-3-methylimidazolium chloride and 1-hexadecyl-3-methyl-imidazolium saccharinate were studied in view of their possible use as phase-change materials. Differential scanning calorimetry (DSC) and the heat-leak modulus (HLM) methods were used to determine the temperatures and the enthalpies of phase transitions in the studied ILs, enabling us to study the influence of the heating and cooling rates on the measured properties. Enthalpies of fusion near to or larger than 100 J·g−1 were found in the studied ionic liquids, making them promising candidates for thermal energy storage. Peaks corresponding to possible liquid crystalline phases in the DSC traces of 1-hexadecyl-3-methylimidazolium saccharinate were observed, pointing to more complex phase behaviour of the studied ionic liquids. Finally, to critically evaluate the experimental data measured in this work, methods based on mathematical gnostics were used. Repeatability of measurements and the degree of mutual agreement between the methods used in this work could thus be determined. © 2019 Elsevier B.V.",
journal = "Journal of Molecular Liquids",
title = "Phase transitions in higher-melting imidazolium-based ionic liquids: Experiments and advanced data analysis",
volume = "292",
pages = "111222",
doi = "10.1016/j.molliq.2019.111222"
}
Čanji, M., Bendova, M., Bogdanov, M. G., Wagner, Z., Zdolšek, N., Quirion, F., Jandová, V.,& Vrbka, P.. (2019). Phase transitions in higher-melting imidazolium-based ionic liquids: Experiments and advanced data analysis. in Journal of Molecular Liquids, 292, 111222.
https://doi.org/10.1016/j.molliq.2019.111222
Čanji M, Bendova M, Bogdanov MG, Wagner Z, Zdolšek N, Quirion F, Jandová V, Vrbka P. Phase transitions in higher-melting imidazolium-based ionic liquids: Experiments and advanced data analysis. in Journal of Molecular Liquids. 2019;292:111222.
doi:10.1016/j.molliq.2019.111222 .
Čanji, Maja, Bendova, Magdalena, Bogdanov, Milen G., Wagner, Zdenek, Zdolšek, Nikola, Quirion, François, Jandová, Věra, Vrbka, Pavel, "Phase transitions in higher-melting imidazolium-based ionic liquids: Experiments and advanced data analysis" in Journal of Molecular Liquids, 292 (2019):111222,
https://doi.org/10.1016/j.molliq.2019.111222 . .
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3

Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction

Zdolšek, Nikola; Dimitrijević, Aleksandra; Bendova, Magdalena; Krstić, Jugoslav B.; Rocha, Raquel P.; Figueiredo, Jose L.; Bajuk-Bogdanović, Danica; Trtić-Petrović, Tatjana M.; Šljukić, Biljana

(2018)

TY  - JOUR
AU  - Zdolšek, Nikola
AU  - Dimitrijević, Aleksandra
AU  - Bendova, Magdalena
AU  - Krstić, Jugoslav B.
AU  - Rocha, Raquel P.
AU  - Figueiredo, Jose L.
AU  - Bajuk-Bogdanović, Danica
AU  - Trtić-Petrović, Tatjana M.
AU  - Šljukić, Biljana
PY  - 2018
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/9881
AB  - Carbon materials, prepared by using different methods with ionic liquids, are compared as electrocatalysts for the oxygen reduction reaction (ORR). Materials were synthesized through the hydrothermal carbonization of glucose and by using the same method in the presence of 1-butyl-3-methylimidazolium methanesulfonate [bmim][MeSO3] as an additive. Another two carbon-based materials were prepared by using ionic-liquid-based methods: ionothermal carbonization of glucose using [bmim][MeSO3] as a recyclable medium for the carbonization reaction and by direct carbonization of the ionic liquid in a one-step method using [bmim][MeSO3] as the precursor for N- and S-doped porous carbon (Carb-IL). Characterization results showed the possibility of morphology and porosity control by using [bmim][MeSO3]. All materials were subsequently tested for the ORR in alkaline media. Carb-IL showed enhanced and stable electrocatalytic ORR activity, even in the presence of methanol, ethanol, and borohydride, opening the possibility for its application in fuel cells.
T2  - Chemelectrochem
T1  - Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction
VL  - 5
IS  - 7
SP  - 1037
EP  - 1046
DO  - 10.1002/celc.201701369
ER  - 
@article{
author = "Zdolšek, Nikola and Dimitrijević, Aleksandra and Bendova, Magdalena and Krstić, Jugoslav B. and Rocha, Raquel P. and Figueiredo, Jose L. and Bajuk-Bogdanović, Danica and Trtić-Petrović, Tatjana M. and Šljukić, Biljana",
year = "2018",
abstract = "Carbon materials, prepared by using different methods with ionic liquids, are compared as electrocatalysts for the oxygen reduction reaction (ORR). Materials were synthesized through the hydrothermal carbonization of glucose and by using the same method in the presence of 1-butyl-3-methylimidazolium methanesulfonate [bmim][MeSO3] as an additive. Another two carbon-based materials were prepared by using ionic-liquid-based methods: ionothermal carbonization of glucose using [bmim][MeSO3] as a recyclable medium for the carbonization reaction and by direct carbonization of the ionic liquid in a one-step method using [bmim][MeSO3] as the precursor for N- and S-doped porous carbon (Carb-IL). Characterization results showed the possibility of morphology and porosity control by using [bmim][MeSO3]. All materials were subsequently tested for the ORR in alkaline media. Carb-IL showed enhanced and stable electrocatalytic ORR activity, even in the presence of methanol, ethanol, and borohydride, opening the possibility for its application in fuel cells.",
journal = "Chemelectrochem",
title = "Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction",
volume = "5",
number = "7",
pages = "1037-1046",
doi = "10.1002/celc.201701369"
}
Zdolšek, N., Dimitrijević, A., Bendova, M., Krstić, J. B., Rocha, R. P., Figueiredo, J. L., Bajuk-Bogdanović, D., Trtić-Petrović, T. M.,& Šljukić, B.. (2018). Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction. in Chemelectrochem, 5(7), 1037-1046.
https://doi.org/10.1002/celc.201701369
Zdolšek N, Dimitrijević A, Bendova M, Krstić JB, Rocha RP, Figueiredo JL, Bajuk-Bogdanović D, Trtić-Petrović TM, Šljukić B. Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction. in Chemelectrochem. 2018;5(7):1037-1046.
doi:10.1002/celc.201701369 .
Zdolšek, Nikola, Dimitrijević, Aleksandra, Bendova, Magdalena, Krstić, Jugoslav B., Rocha, Raquel P., Figueiredo, Jose L., Bajuk-Bogdanović, Danica, Trtić-Petrović, Tatjana M., Šljukić, Biljana, "Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction" in Chemelectrochem, 5, no. 7 (2018):1037-1046,
https://doi.org/10.1002/celc.201701369 . .
1
16
14
16

Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction

Zdolšek, Nikola; Dimitrijević, Aleksandra; Bendova, Magdalena; Krstić, Jugoslav B.; Rocha, Raquel P.; Figueiredo, Jose L.; Bajuk-Bogdanović, Danica V.; Trtić-Petrović, Tatjana M.; Šljukić, Biljana

(2018)

TY  - JOUR
AU  - Zdolšek, Nikola
AU  - Dimitrijević, Aleksandra
AU  - Bendova, Magdalena
AU  - Krstić, Jugoslav B.
AU  - Rocha, Raquel P.
AU  - Figueiredo, Jose L.
AU  - Bajuk-Bogdanović, Danica V.
AU  - Trtić-Petrović, Tatjana M.
AU  - Šljukić, Biljana
PY  - 2018
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7672
AB  - Carbon materials, prepared by using different methods with ionicliquids, are compared as electrocatalysts for the oxygen reductionreaction (ORR). Materials were synthesized through the hydrothermalcarbonization of glucose and by using the same method in the presence of1-butyl-3-methylimidazolium methanesulfonate {[}bmim]{[}MeSO3] as anadditive. Another two carbon-based materials were prepared by usingionic-liquid-based methods: ionothermal carbonization of glucose using{[}bmim]{[}MeSO3] as a recyclable medium for the carbonization reactionand by direct carbonization of the ionic liquid in a one-step methodusing {[}bmim]{[}MeSO3] as the precursor for N- and S-doped porouscarbon (Carb-IL). Characterization results showed the possibility ofmorphology and porosity control by using {[}bmim]{[}MeSO3]. Allmaterials were subsequently tested for the ORR in alkaline media.Carb-IL showed enhanced and stable electrocatalytic ORR activity, evenin the presence of methanol, ethanol, and borohydride, opening thepossibility for its application in fuel cells.
T2  - ChemElectroChem
T1  - Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction
VL  - 5
IS  - 7
SP  - 1037
EP  - 1046
DO  - 10.1002/celc.201701369
ER  - 
@article{
author = "Zdolšek, Nikola and Dimitrijević, Aleksandra and Bendova, Magdalena and Krstić, Jugoslav B. and Rocha, Raquel P. and Figueiredo, Jose L. and Bajuk-Bogdanović, Danica V. and Trtić-Petrović, Tatjana M. and Šljukić, Biljana",
year = "2018",
abstract = "Carbon materials, prepared by using different methods with ionicliquids, are compared as electrocatalysts for the oxygen reductionreaction (ORR). Materials were synthesized through the hydrothermalcarbonization of glucose and by using the same method in the presence of1-butyl-3-methylimidazolium methanesulfonate {[}bmim]{[}MeSO3] as anadditive. Another two carbon-based materials were prepared by usingionic-liquid-based methods: ionothermal carbonization of glucose using{[}bmim]{[}MeSO3] as a recyclable medium for the carbonization reactionand by direct carbonization of the ionic liquid in a one-step methodusing {[}bmim]{[}MeSO3] as the precursor for N- and S-doped porouscarbon (Carb-IL). Characterization results showed the possibility ofmorphology and porosity control by using {[}bmim]{[}MeSO3]. Allmaterials were subsequently tested for the ORR in alkaline media.Carb-IL showed enhanced and stable electrocatalytic ORR activity, evenin the presence of methanol, ethanol, and borohydride, opening thepossibility for its application in fuel cells.",
journal = "ChemElectroChem",
title = "Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction",
volume = "5",
number = "7",
pages = "1037-1046",
doi = "10.1002/celc.201701369"
}
Zdolšek, N., Dimitrijević, A., Bendova, M., Krstić, J. B., Rocha, R. P., Figueiredo, J. L., Bajuk-Bogdanović, D. V., Trtić-Petrović, T. M.,& Šljukić, B.. (2018). Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction. in ChemElectroChem, 5(7), 1037-1046.
https://doi.org/10.1002/celc.201701369
Zdolšek N, Dimitrijević A, Bendova M, Krstić JB, Rocha RP, Figueiredo JL, Bajuk-Bogdanović DV, Trtić-Petrović TM, Šljukić B. Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction. in ChemElectroChem. 2018;5(7):1037-1046.
doi:10.1002/celc.201701369 .
Zdolšek, Nikola, Dimitrijević, Aleksandra, Bendova, Magdalena, Krstić, Jugoslav B., Rocha, Raquel P., Figueiredo, Jose L., Bajuk-Bogdanović, Danica V., Trtić-Petrović, Tatjana M., Šljukić, Biljana, "Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction" in ChemElectroChem, 5, no. 7 (2018):1037-1046,
https://doi.org/10.1002/celc.201701369 . .
1
16
14
16

New sample preparation method based on task-specific ionic liquids for extraction and determination of copper in urine and wastewater

Trtić-Petrović, Tatjana M.; Dimitrijević, Aleksandra; Zdolšek, Nikola; Đorđević, Jelena S.; Tot, Aleksandar; Vraneš, Milan; Gadžurić, Slobodan

(2018)

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 . .
1
10
8
11

Phase transitions in higher-melting ionic liquids: Thermal storage materials or liquid crystals?

Bendova, Magdalena; Čanjia, Maja; Bogdanov, Milen G.; Wagner, Zdenek; Zdolšek, Nikola; Quirion, François

(2018)

TY  - JOUR
AU  - Bendova, Magdalena
AU  - Čanjia, Maja
AU  - Bogdanov, Milen G.
AU  - Wagner, Zdenek
AU  - Zdolšek, Nikola
AU  - Quirion, François
PY  - 2018
UR  - https://www.scopus.com/inward/record.uri?eid=2-s2.0-85054697195&doi=10.3303%2FCET1869007&partnerID=40&md5=46569c93dc128032eb41f076cbd1bf23
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7910
AB  - To assess the application potential of a material in thermal energy storage, the knowledge of their thermophysical properties is of key importance. Specifically, an efficient material has to show, among others, large enthalpies of phase change and a sufficiently large thermal conductivity. In this work, imidazolium-based ionic liquids (ILs) with long alkyl chain substituents 1-hexadecyl-3-methylimidazolium chloride and 1-hexadecyl-3-methylimidazolium saccharinate were studied in view of their possible use as phase-change materials. Differential scanning calorimetry (DSC) and the heat-leak modulus methods were used to determine the temperatures and the enthalpies of phase transitions in the studied ILs, enabling us to study the influence of the heating rates on the measured properties. Enthalpies of fusion near to or larger than 100 J·g-1 were found in the studied ionic liquids, making them promising candidates for thermal energy storage. Furthermore, peaks corresponding to possible liquid crystalline phases in the DSC traces of 1-hexadecyl-3-methylimidazolium saccharinate were observed. The measured properties are not only essential characteristics of a thermal storage material, temperatures and enthalpies of melting are necessary in thermodynamic description and modelling of solid-liquid phase behavior and thus in the possible utilization of the material in separation and crystallization processes. © Copyright 2018, AIDIC Servizi S.r.l.
T2  - Chemical Engineering Transactions
T1  - Phase transitions in higher-melting ionic liquids: Thermal storage materials or liquid crystals?
VL  - 69
SP  - 37
EP  - 42
DO  - 10.3303/CET1869007
ER  - 
@article{
author = "Bendova, Magdalena and Čanjia, Maja and Bogdanov, Milen G. and Wagner, Zdenek and Zdolšek, Nikola and Quirion, François",
year = "2018",
abstract = "To assess the application potential of a material in thermal energy storage, the knowledge of their thermophysical properties is of key importance. Specifically, an efficient material has to show, among others, large enthalpies of phase change and a sufficiently large thermal conductivity. In this work, imidazolium-based ionic liquids (ILs) with long alkyl chain substituents 1-hexadecyl-3-methylimidazolium chloride and 1-hexadecyl-3-methylimidazolium saccharinate were studied in view of their possible use as phase-change materials. Differential scanning calorimetry (DSC) and the heat-leak modulus methods were used to determine the temperatures and the enthalpies of phase transitions in the studied ILs, enabling us to study the influence of the heating rates on the measured properties. Enthalpies of fusion near to or larger than 100 J·g-1 were found in the studied ionic liquids, making them promising candidates for thermal energy storage. Furthermore, peaks corresponding to possible liquid crystalline phases in the DSC traces of 1-hexadecyl-3-methylimidazolium saccharinate were observed. The measured properties are not only essential characteristics of a thermal storage material, temperatures and enthalpies of melting are necessary in thermodynamic description and modelling of solid-liquid phase behavior and thus in the possible utilization of the material in separation and crystallization processes. © Copyright 2018, AIDIC Servizi S.r.l.",
journal = "Chemical Engineering Transactions",
title = "Phase transitions in higher-melting ionic liquids: Thermal storage materials or liquid crystals?",
volume = "69",
pages = "37-42",
doi = "10.3303/CET1869007"
}
Bendova, M., Čanjia, M., Bogdanov, M. G., Wagner, Z., Zdolšek, N.,& Quirion, F.. (2018). Phase transitions in higher-melting ionic liquids: Thermal storage materials or liquid crystals?. in Chemical Engineering Transactions, 69, 37-42.
https://doi.org/10.3303/CET1869007
Bendova M, Čanjia M, Bogdanov MG, Wagner Z, Zdolšek N, Quirion F. Phase transitions in higher-melting ionic liquids: Thermal storage materials or liquid crystals?. in Chemical Engineering Transactions. 2018;69:37-42.
doi:10.3303/CET1869007 .
Bendova, Magdalena, Čanjia, Maja, Bogdanov, Milen G., Wagner, Zdenek, Zdolšek, Nikola, Quirion, François, "Phase transitions in higher-melting ionic liquids: Thermal storage materials or liquid crystals?" in Chemical Engineering Transactions, 69 (2018):37-42,
https://doi.org/10.3303/CET1869007 . .
1

Solid-phase extraction disk based on multiwalled carbon nanotubes for the enrichment of targeted pesticides from aqueous samples

Zdolšek, Nikola; Kumrić, Ksenija; Kalijadis, Ana; Trtić-Petrović, Tatjana M.

(2017)

TY  - JOUR
AU  - Zdolšek, Nikola
AU  - Kumrić, Ksenija
AU  - Kalijadis, Ana
AU  - Trtić-Petrović, Tatjana M.
PY  - 2017
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1527
AB  - A sensitive method for the determination of six varying polarity pesticides (imidacloprid, acetamiprid, carbendazim, simazine, linuron, and tebufenozide) based on a solid-phase extraction disk with multiwalled nanotubes is proposed. A dispersion of multiwalled nanotubes in a surfactant aqueous solution (Triton X-100) was used for the preparation of the solid-phase extraction disk. The effect of surfactant on the functional groups of multiwalled nanotubes was examined by applying temperature-programmed desorption. It was found that this treatment increased the amount of oxygen groups of treated multiwalled nanotubes comparing with untreated ones. The factors that may influence the adsorption and recovery such as the kind and volume of eluent, volume, flow rate and pH of sample were investigated and optimized. Under the optimized conditions, the maximal enrichment factors for low polar pesticides are ranging from 4000 to 4985 and for more polar are 2250 and 2750. The linear range of calibration curves was 10-500 ng/L with correlation coefficient higher than 0.9960, and the detection limit was 6.2-23.7 ng/L. Finally optimized method was applied for determination trace level of five out of six pesticides in tap and river water samples with good recovery.
T2  - Journal of Separation Science
T1  - Solid-phase extraction disk based on multiwalled carbon nanotubes for the enrichment of targeted pesticides from aqueous samples
VL  - 40
IS  - 7
SP  - 1564
EP  - 1571
DO  - 10.1002/jssc.201600957
ER  - 
@article{
author = "Zdolšek, Nikola and Kumrić, Ksenija and Kalijadis, Ana and Trtić-Petrović, Tatjana M.",
year = "2017",
abstract = "A sensitive method for the determination of six varying polarity pesticides (imidacloprid, acetamiprid, carbendazim, simazine, linuron, and tebufenozide) based on a solid-phase extraction disk with multiwalled nanotubes is proposed. A dispersion of multiwalled nanotubes in a surfactant aqueous solution (Triton X-100) was used for the preparation of the solid-phase extraction disk. The effect of surfactant on the functional groups of multiwalled nanotubes was examined by applying temperature-programmed desorption. It was found that this treatment increased the amount of oxygen groups of treated multiwalled nanotubes comparing with untreated ones. The factors that may influence the adsorption and recovery such as the kind and volume of eluent, volume, flow rate and pH of sample were investigated and optimized. Under the optimized conditions, the maximal enrichment factors for low polar pesticides are ranging from 4000 to 4985 and for more polar are 2250 and 2750. The linear range of calibration curves was 10-500 ng/L with correlation coefficient higher than 0.9960, and the detection limit was 6.2-23.7 ng/L. Finally optimized method was applied for determination trace level of five out of six pesticides in tap and river water samples with good recovery.",
journal = "Journal of Separation Science",
title = "Solid-phase extraction disk based on multiwalled carbon nanotubes for the enrichment of targeted pesticides from aqueous samples",
volume = "40",
number = "7",
pages = "1564-1571",
doi = "10.1002/jssc.201600957"
}
Zdolšek, N., Kumrić, K., Kalijadis, A.,& Trtić-Petrović, T. M.. (2017). Solid-phase extraction disk based on multiwalled carbon nanotubes for the enrichment of targeted pesticides from aqueous samples. in Journal of Separation Science, 40(7), 1564-1571.
https://doi.org/10.1002/jssc.201600957
Zdolšek N, Kumrić K, Kalijadis A, Trtić-Petrović TM. Solid-phase extraction disk based on multiwalled carbon nanotubes for the enrichment of targeted pesticides from aqueous samples. in Journal of Separation Science. 2017;40(7):1564-1571.
doi:10.1002/jssc.201600957 .
Zdolšek, Nikola, Kumrić, Ksenija, Kalijadis, Ana, Trtić-Petrović, Tatjana M., "Solid-phase extraction disk based on multiwalled carbon nanotubes for the enrichment of targeted pesticides from aqueous samples" in Journal of Separation Science, 40, no. 7 (2017):1564-1571,
https://doi.org/10.1002/jssc.201600957 . .
7
6
6

Aqueous biphasic system formation using 1-alkyl-3-ethylimidazolium bromide ionic liquids as new extractants

Dimitrijević, Aleksandra; Zec, Nebojša; Zdolšek, Nikola; Dožić, Sanja; Tot, Aleksandar; Gadžurić, Slobodan; Vraneš, Milan; Trtić-Petrović, Tatjana M.

(2016)

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 . .
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