TY  - CONF
AU  - Nikolić, Željka
AU  - Milovanović, Dubravka
AU  - Marčeta Kaninski, Milica
AU  - Nikolić, Vladimir
AU  - Radulović, Aleksandra
AU  - Tasić, A
PY  - 2023
UR  - https://riofh.iofh.bg.ac.rs/handle/123456789/1065
PB  - Srpsko hemijsko društvo/Serbian Chemical Society
C3  - Knjiga izvoda, 9. Simpozijum „Hemija i zaštita životne sredine ENVIROCHEM2023“
T1  - Organic acids as solvents for leaching PAHs out of impregnated wood
ER  - 

@conference{
author = "Nikolić, Željka and Milovanović, Dubravka and Marčeta Kaninski, Milica and Nikolić, Vladimir and Radulović, Aleksandra and Tasić, A",
year = "2023",
publisher = "Srpsko hemijsko društvo/Serbian Chemical Society",
journal = "Knjiga izvoda, 9. Simpozijum „Hemija i zaštita životne sredine ENVIROCHEM2023“",
title = "Organic acids as solvents for leaching PAHs out of impregnated wood"
}

Nikolić, Ž., Milovanović, D., Marčeta Kaninski, M., Nikolić, V., Radulović, A.,& Tasić, A.. (2023). Organic acids as solvents for leaching PAHs out of impregnated wood. in Knjiga izvoda, 9. Simpozijum „Hemija i zaštita životne sredine ENVIROCHEM2023“
Srpsko hemijsko društvo/Serbian Chemical Society..

Nikolić Ž, Milovanović D, Marčeta Kaninski M, Nikolić V, Radulović A, Tasić A. Organic acids as solvents for leaching PAHs out of impregnated wood. in Knjiga izvoda, 9. Simpozijum „Hemija i zaštita životne sredine ENVIROCHEM2023“. 2023;..

Nikolić, Željka, Milovanović, Dubravka, Marčeta Kaninski, Milica, Nikolić, Vladimir, Radulović, Aleksandra, Tasić, A, "Organic acids as solvents for leaching PAHs out of impregnated wood" in Knjiga izvoda, 9. Simpozijum „Hemija i zaštita životne sredine ENVIROCHEM2023“ (2023).

TY  - JOUR
AU  - Popović, Predrag
AU  - Stjelja, Živko
AU  - Miletić, Branimir
AU  - Vranješ, Đorđe
AU  - Stojanović, Veljko
AU  - Nikolić, Vladimir
AU  - Marčeta-Kaninski, Milica
PY  - 2022
UR  - https://riofh.iofh.bg.ac.rs/handle/123456789/887
AB  - Ispitivanje električnih vozila (EV) daleko prevazilazi zahteve homologacionih ispitivanja motornih vozila i njihovih komponenti. Električna motorna vozila na vodonične gorivne ćelije (FCV-eng. Fuel Cell vehicles) su veoma slična električnim vozilima, u smislu da za pokretanje vozila koriste elektromotor umesto motora sa unutrašnjim sagorevanjem. Glavna razlika je ta da EV koriste baterije, koje se moraju priključiti na mrežu radi punjenja, dok FCV proizvode električnu energiju na licu mesta. Ovaj rad predstavlja pregled regulativa o ispitivanju i kontrolisanju električnih vozila na vodonik. Ispitivanje motornih vozila danas predstavlja spektar raznih testiranja koja se odigravaju u različitim stadijumima razvoja vozila, proizvodnje i upotrebe vozila, a čiji je zadatak da obezbedi dobijanje objektivnih informacija o kvalitetu vozila, njihovih sklopova i komponenti, o uslovima rada, okruženju i sl. Legislativa koja se odnosi na ispitivanje motornih vozila na vodonik postoji, ali se odgovarajuće procedure i standardi i dalje razvijaju, u korak sa napretkom tehnologije.
AB  - Hydrogen Fuel Cell Vehicles (FCVs) are similar to EVs, in the aspect that they use an electric motor instead of an internal combustion engine to power the wheels. The main difference is that EVs run on batteries that must be plugged in to recharge, while FCVs generate their electricity onboard. This manuscript presents overview of the hydrogen vehicle certification legislation. Inspection and testing of motor vehicle technology today represent a set of a whole series of procedures that are applied in different stages of the vehicle development, production and operation of vehicles, and whose task is to provide objective information about the quality of the vehicle and its assemblies and parts, as well as about the conditions in which the vehicles operate, about workloads, environment, etc. Although there are adopted technical regulative for hydrogen powered EVs, the appropriate standards and legislation are still evolving.
PB  - Univerzitet u Beogradu - Poljoprivredni fakultet - Institut za poljoprivrednu tehniku, Beograd
T2  - Poljoprivredna tehnika
T1  - Električna motorna vozila na vodonik - trendovi ispitivanja i kontrolisanja
T1  - Hydrogen electric motor vehicles: Testing and control trends
EP  - 93
IS  - 4
SP  - 82
VL  - 47
DO  - 10.5937/PoljTeh2204082P
UR  - conv_78
ER  - 

@article{
author = "Popović, Predrag and Stjelja, Živko and Miletić, Branimir and Vranješ, Đorđe and Stojanović, Veljko and Nikolić, Vladimir and Marčeta-Kaninski, Milica",
year = "2022",
abstract = "Ispitivanje električnih vozila (EV) daleko prevazilazi zahteve homologacionih ispitivanja motornih vozila i njihovih komponenti. Električna motorna vozila na vodonične gorivne ćelije (FCV-eng. Fuel Cell vehicles) su veoma slična električnim vozilima, u smislu da za pokretanje vozila koriste elektromotor umesto motora sa unutrašnjim sagorevanjem. Glavna razlika je ta da EV koriste baterije, koje se moraju priključiti na mrežu radi punjenja, dok FCV proizvode električnu energiju na licu mesta. Ovaj rad predstavlja pregled regulativa o ispitivanju i kontrolisanju električnih vozila na vodonik. Ispitivanje motornih vozila danas predstavlja spektar raznih testiranja koja se odigravaju u različitim stadijumima razvoja vozila, proizvodnje i upotrebe vozila, a čiji je zadatak da obezbedi dobijanje objektivnih informacija o kvalitetu vozila, njihovih sklopova i komponenti, o uslovima rada, okruženju i sl. Legislativa koja se odnosi na ispitivanje motornih vozila na vodonik postoji, ali se odgovarajuće procedure i standardi i dalje razvijaju, u korak sa napretkom tehnologije., Hydrogen Fuel Cell Vehicles (FCVs) are similar to EVs, in the aspect that they use an electric motor instead of an internal combustion engine to power the wheels. The main difference is that EVs run on batteries that must be plugged in to recharge, while FCVs generate their electricity onboard. This manuscript presents overview of the hydrogen vehicle certification legislation. Inspection and testing of motor vehicle technology today represent a set of a whole series of procedures that are applied in different stages of the vehicle development, production and operation of vehicles, and whose task is to provide objective information about the quality of the vehicle and its assemblies and parts, as well as about the conditions in which the vehicles operate, about workloads, environment, etc. Although there are adopted technical regulative for hydrogen powered EVs, the appropriate standards and legislation are still evolving.",
publisher = "Univerzitet u Beogradu - Poljoprivredni fakultet - Institut za poljoprivrednu tehniku, Beograd",
journal = "Poljoprivredna tehnika",
title = "Električna motorna vozila na vodonik - trendovi ispitivanja i kontrolisanja, Hydrogen electric motor vehicles: Testing and control trends",
pages = "93-82",
number = "4",
volume = "47",
doi = "10.5937/PoljTeh2204082P",
url = "conv_78"
}

Popović, P., Stjelja, Ž., Miletić, B., Vranješ, Đ., Stojanović, V., Nikolić, V.,& Marčeta-Kaninski, M.. (2022). Električna motorna vozila na vodonik - trendovi ispitivanja i kontrolisanja. in Poljoprivredna tehnika
Univerzitet u Beogradu - Poljoprivredni fakultet - Institut za poljoprivrednu tehniku, Beograd., 47(4), 82-93.
https://doi.org/10.5937/PoljTeh2204082P
conv_78

Popović P, Stjelja Ž, Miletić B, Vranješ Đ, Stojanović V, Nikolić V, Marčeta-Kaninski M. Električna motorna vozila na vodonik - trendovi ispitivanja i kontrolisanja. in Poljoprivredna tehnika. 2022;47(4):82-93.
doi:10.5937/PoljTeh2204082P
conv_78 .

Popović, Predrag, Stjelja, Živko, Miletić, Branimir, Vranješ, Đorđe, Stojanović, Veljko, Nikolić, Vladimir, Marčeta-Kaninski, Milica, "Električna motorna vozila na vodonik - trendovi ispitivanja i kontrolisanja" in Poljoprivredna tehnika, 47, no. 4 (2022):82-93,
https://doi.org/10.5937/PoljTeh2204082P .,
conv_78 .

TY  - GEN
AU  - Marinković, Miloš
AU  - Milovanović, Dubravka
AU  - Waisi, Hadi
AU  - Hreščak, Jitka
AU  - Rajčić, Boris
AU  - Marčeta Kaninski, Milica
AU  - Nikolić, Vladimir
AU  - Blagojević, Stevan
PY  - 2021
UR  - https://riofh.iofh.bg.ac.rs/handle/123456789/1021
T1  - SVILENA ZAŠTITNA MASKA SA NANOČESTICAMA SREBRA
ER  - 

@misc{
author = "Marinković, Miloš and Milovanović, Dubravka and Waisi, Hadi and Hreščak, Jitka and Rajčić, Boris and Marčeta Kaninski, Milica and Nikolić, Vladimir and Blagojević, Stevan",
year = "2021",
title = "SVILENA ZAŠTITNA MASKA SA NANOČESTICAMA SREBRA"
}

Marinković, M., Milovanović, D., Waisi, H., Hreščak, J., Rajčić, B., Marčeta Kaninski, M., Nikolić, V.,& Blagojević, S.. (2021). SVILENA ZAŠTITNA MASKA SA NANOČESTICAMA SREBRA. .

Marinković M, Milovanović D, Waisi H, Hreščak J, Rajčić B, Marčeta Kaninski M, Nikolić V, Blagojević S. SVILENA ZAŠTITNA MASKA SA NANOČESTICAMA SREBRA. 2021;..

Marinković, Miloš, Milovanović, Dubravka, Waisi, Hadi, Hreščak, Jitka, Rajčić, Boris, Marčeta Kaninski, Milica, Nikolić, Vladimir, Blagojević, Stevan, "SVILENA ZAŠTITNA MASKA SA NANOČESTICAMA SREBRA" (2021).

TY  - GEN
AU  - Šaponjić, Zoran
AU  - Waisi, Hadi
AU  - Marinković, Miloš
AU  - Marčeta Kaninski, Milica
AU  - Nikolić, Vladimir
AU  - Milovanović, Dubravka
AU  - Rajčić, Boris
AU  - Blagojević, Stevan
PY  - 2021
UR  - https://riofh.iofh.bg.ac.rs/handle/123456789/1022
T1  - FORMIRANJE NOVIH PROIZVODA ZA PROIZVODNJU BETONSKIH ELEMENATA ILI ADITIVA, NA BAZI WASTE-TO-PRODUCT PRINCIPA
ER  - 

@misc{
author = "Šaponjić, Zoran and Waisi, Hadi and Marinković, Miloš and Marčeta Kaninski, Milica and Nikolić, Vladimir and Milovanović, Dubravka and Rajčić, Boris and Blagojević, Stevan",
year = "2021",
title = "FORMIRANJE NOVIH PROIZVODA ZA PROIZVODNJU BETONSKIH ELEMENATA ILI ADITIVA, NA BAZI WASTE-TO-PRODUCT PRINCIPA"
}

Šaponjić, Z., Waisi, H., Marinković, M., Marčeta Kaninski, M., Nikolić, V., Milovanović, D., Rajčić, B.,& Blagojević, S.. (2021). FORMIRANJE NOVIH PROIZVODA ZA PROIZVODNJU BETONSKIH ELEMENATA ILI ADITIVA, NA BAZI WASTE-TO-PRODUCT PRINCIPA. .

Šaponjić Z, Waisi H, Marinković M, Marčeta Kaninski M, Nikolić V, Milovanović D, Rajčić B, Blagojević S. FORMIRANJE NOVIH PROIZVODA ZA PROIZVODNJU BETONSKIH ELEMENATA ILI ADITIVA, NA BAZI WASTE-TO-PRODUCT PRINCIPA. 2021;..

Šaponjić, Zoran, Waisi, Hadi, Marinković, Miloš, Marčeta Kaninski, Milica, Nikolić, Vladimir, Milovanović, Dubravka, Rajčić, Boris, Blagojević, Stevan, "FORMIRANJE NOVIH PROIZVODA ZA PROIZVODNJU BETONSKIH ELEMENATA ILI ADITIVA, NA BAZI WASTE-TO-PRODUCT PRINCIPA" (2021).

TY  - JOUR
AU  - Marčeta-Kaninski, Milica
AU  - Šaponjić, Zoran
AU  - Mudrinić, Mihajlo
AU  - Milovanović, Dubravka
AU  - Rajčić, Boris
AU  - Radulović, Aleksandra
AU  - Nikolić, Vladimir
PY  - 2021
UR  - https://riofh.iofh.bg.ac.rs/handle/123456789/776
AB  - The article presents promising catalysts, applicable for direct alcohol fuel cells (DAFC) for portable and mobile applications. The goal of this work is development of Pt and Pd catalysts deposited on interactive nanocrystalline Ru doped SnO2 support with improved performance. The structure and the morphology of the prepared metal-oxide catalyst support and Pt and Pd based catalysts were examined using XRPD, SEM/EDX and TEM techniques. Electrocatalytic activities of the prepared Pt or Pd based catalysts were evaluated in both alkaline and acidic conditions. The ethanol oxidation reaction (EOR) was studied using conventional electrochemical techniques. The interactive nature of the novel Ru doped SnO2 catalyst support was confirmed, resulting in the enhancement of the EOR kinetics, in comparison to commercially available catalysts. New and simplified synthetic route applied for preparation of interactive catalyst support was presented with the aim to enable easy scale-up of the catalyst production process. Obtained results on the novel catalysts promise great potential in improving the performance and durability of the DAFC.
T2  - International Journal of Hydrogen Energy
T1  - Comparison of Pt and Pd anode catalysts supported on nanocrystalline Ru-SnO2 for ethanol oxidation in fuel cell applications
EP  - 38280
IS  - 77
SP  - 38270
VL  - 46
DO  - 10.1016/j.ijhydene.2021.09.088
UR  - conv_963
ER  - 

@article{
author = "Marčeta-Kaninski, Milica and Šaponjić, Zoran and Mudrinić, Mihajlo and Milovanović, Dubravka and Rajčić, Boris and Radulović, Aleksandra and Nikolić, Vladimir",
year = "2021",
abstract = "The article presents promising catalysts, applicable for direct alcohol fuel cells (DAFC) for portable and mobile applications. The goal of this work is development of Pt and Pd catalysts deposited on interactive nanocrystalline Ru doped SnO2 support with improved performance. The structure and the morphology of the prepared metal-oxide catalyst support and Pt and Pd based catalysts were examined using XRPD, SEM/EDX and TEM techniques. Electrocatalytic activities of the prepared Pt or Pd based catalysts were evaluated in both alkaline and acidic conditions. The ethanol oxidation reaction (EOR) was studied using conventional electrochemical techniques. The interactive nature of the novel Ru doped SnO2 catalyst support was confirmed, resulting in the enhancement of the EOR kinetics, in comparison to commercially available catalysts. New and simplified synthetic route applied for preparation of interactive catalyst support was presented with the aim to enable easy scale-up of the catalyst production process. Obtained results on the novel catalysts promise great potential in improving the performance and durability of the DAFC.",
journal = "International Journal of Hydrogen Energy",
title = "Comparison of Pt and Pd anode catalysts supported on nanocrystalline Ru-SnO2 for ethanol oxidation in fuel cell applications",
pages = "38280-38270",
number = "77",
volume = "46",
doi = "10.1016/j.ijhydene.2021.09.088",
url = "conv_963"
}

Marčeta-Kaninski, M., Šaponjić, Z., Mudrinić, M., Milovanović, D., Rajčić, B., Radulović, A.,& Nikolić, V.. (2021). Comparison of Pt and Pd anode catalysts supported on nanocrystalline Ru-SnO2 for ethanol oxidation in fuel cell applications. in International Journal of Hydrogen Energy, 46(77), 38270-38280.
https://doi.org/10.1016/j.ijhydene.2021.09.088
conv_963

Marčeta-Kaninski M, Šaponjić Z, Mudrinić M, Milovanović D, Rajčić B, Radulović A, Nikolić V. Comparison of Pt and Pd anode catalysts supported on nanocrystalline Ru-SnO2 for ethanol oxidation in fuel cell applications. in International Journal of Hydrogen Energy. 2021;46(77):38270-38280.
doi:10.1016/j.ijhydene.2021.09.088
conv_963 .

Marčeta-Kaninski, Milica, Šaponjić, Zoran, Mudrinić, Mihajlo, Milovanović, Dubravka, Rajčić, Boris, Radulović, Aleksandra, Nikolić, Vladimir, "Comparison of Pt and Pd anode catalysts supported on nanocrystalline Ru-SnO2 for ethanol oxidation in fuel cell applications" in International Journal of Hydrogen Energy, 46, no. 77 (2021):38270-38280,
https://doi.org/10.1016/j.ijhydene.2021.09.088 .,
conv_963 .

TY  - GEN
AU  - Waisi, Hadi
AU  - Marinković, Miloš
AU  - Rajčić, Boris
AU  - Milovanović, Dubravka
AU  - Marčeta Kaninski, Milica
AU  - Šaponjić, Zoran
AU  - Blagojević, Stevan
AU  - Nikolić, Vladimir
PY  - 2020
UR  - https://riofh.iofh.bg.ac.rs/handle/123456789/1023
T1  - VIŠEKRATNA ZAŠTITNA MASKA SA AKTIVNIM UGLJEM
ER  - 

@misc{
author = "Waisi, Hadi and Marinković, Miloš and Rajčić, Boris and Milovanović, Dubravka and Marčeta Kaninski, Milica and Šaponjić, Zoran and Blagojević, Stevan and Nikolić, Vladimir",
year = "2020",
title = "VIŠEKRATNA ZAŠTITNA MASKA SA AKTIVNIM UGLJEM"
}

Waisi, H., Marinković, M., Rajčić, B., Milovanović, D., Marčeta Kaninski, M., Šaponjić, Z., Blagojević, S.,& Nikolić, V.. (2020). VIŠEKRATNA ZAŠTITNA MASKA SA AKTIVNIM UGLJEM. .

Waisi H, Marinković M, Rajčić B, Milovanović D, Marčeta Kaninski M, Šaponjić Z, Blagojević S, Nikolić V. VIŠEKRATNA ZAŠTITNA MASKA SA AKTIVNIM UGLJEM. 2020;..

Waisi, Hadi, Marinković, Miloš, Rajčić, Boris, Milovanović, Dubravka, Marčeta Kaninski, Milica, Šaponjić, Zoran, Blagojević, Stevan, Nikolić, Vladimir, "VIŠEKRATNA ZAŠTITNA MASKA SA AKTIVNIM UGLJEM" (2020).

TY  - GEN
AU  - Milovanović, Dubravka
AU  - Marinković, Miloš
AU  - Waisi, Hadi
AU  - Nikolić, Vladimir
AU  - Rajčić, Boris
AU  - Blagojević, Stevan
AU  - Šaponjić, Zoran
AU  - Marčeta Kaninski, Milica
PY  - 2020
UR  - https://riofh.iofh.bg.ac.rs/handle/123456789/1020
T1  - Nova formulacija sredstava za dezinfekciju i suvo pranje ruku STOP MIKROORGANIZMIMA
ER  - 

@misc{
author = "Milovanović, Dubravka and Marinković, Miloš and Waisi, Hadi and Nikolić, Vladimir and Rajčić, Boris and Blagojević, Stevan and Šaponjić, Zoran and Marčeta Kaninski, Milica",
year = "2020",
title = "Nova formulacija sredstava za dezinfekciju i suvo pranje ruku STOP MIKROORGANIZMIMA"
}

Milovanović, D., Marinković, M., Waisi, H., Nikolić, V., Rajčić, B., Blagojević, S., Šaponjić, Z.,& Marčeta Kaninski, M.. (2020). Nova formulacija sredstava za dezinfekciju i suvo pranje ruku STOP MIKROORGANIZMIMA. .

Milovanović D, Marinković M, Waisi H, Nikolić V, Rajčić B, Blagojević S, Šaponjić Z, Marčeta Kaninski M. Nova formulacija sredstava za dezinfekciju i suvo pranje ruku STOP MIKROORGANIZMIMA. 2020;..

Milovanović, Dubravka, Marinković, Miloš, Waisi, Hadi, Nikolić, Vladimir, Rajčić, Boris, Blagojević, Stevan, Šaponjić, Zoran, Marčeta Kaninski, Milica, "Nova formulacija sredstava za dezinfekciju i suvo pranje ruku STOP MIKROORGANIZMIMA" (2020).

TY  - GEN
AU  - Marinković, Miloš
AU  - Šaponjić, Đorđe
AU  - Blagojević, Stevan
AU  - Nikolić, Vladimir
AU  - Marčeta Kaninski, Milica
AU  - Milovanović, Dubravka
AU  - Rajčić, Boris
AU  - Waisi, Hadi
AU  - Šaponjić, Zoran
PY  - 2020
UR  - https://riofh.iofh.bg.ac.rs/handle/123456789/1019
T1  - DEZINFEKCIJA ZATVORENOG PROSTORA KORIŠĆENJEM OZONA
ER  - 

@misc{
author = "Marinković, Miloš and Šaponjić, Đorđe and Blagojević, Stevan and Nikolić, Vladimir and Marčeta Kaninski, Milica and Milovanović, Dubravka and Rajčić, Boris and Waisi, Hadi and Šaponjić, Zoran",
year = "2020",
title = "DEZINFEKCIJA ZATVORENOG PROSTORA KORIŠĆENJEM OZONA"
}

Marinković, M., Šaponjić, Đ., Blagojević, S., Nikolić, V., Marčeta Kaninski, M., Milovanović, D., Rajčić, B., Waisi, H.,& Šaponjić, Z.. (2020). DEZINFEKCIJA ZATVORENOG PROSTORA KORIŠĆENJEM OZONA. .

Marinković M, Šaponjić Đ, Blagojević S, Nikolić V, Marčeta Kaninski M, Milovanović D, Rajčić B, Waisi H, Šaponjić Z. DEZINFEKCIJA ZATVORENOG PROSTORA KORIŠĆENJEM OZONA. 2020;..

Marinković, Miloš, Šaponjić, Đorđe, Blagojević, Stevan, Nikolić, Vladimir, Marčeta Kaninski, Milica, Milovanović, Dubravka, Rajčić, Boris, Waisi, Hadi, Šaponjić, Zoran, "DEZINFEKCIJA ZATVORENOG PROSTORA KORIŠĆENJEM OZONA" (2020).

TY  - JOUR
AU  - Brković, Snežana
AU  - Marčeta-Kaninski, Milica
AU  - Lausević, Petar Z.
AU  - Šaponjić, Aleksandra B.
AU  - Radulović, Aleksandra
AU  - Rakić, Aleksandra A.
AU  - Pasti, Igor A.
AU  - Nikolić, Vladimir
PY  - 2020
UR  - https://riofh.iofh.bg.ac.rs/handle/123456789/766
AB  - Durability and cost of Proton Exchange Membrane fuel cells (PEMFCs) are two major factors delaying their commercialization. Cost is associated with the price of the catalysts, while durability is associated with degradation and poisoning of the catalysts, primarily by CO. This motivated us to develop tungsten-carbide-oxide (WxCyOz) as a new non-carbon based catalyst support for Pt-Ru-based anode PEMFC catalyst. The aim was to improve performance and obtain higher CO tolerance compared to commercial catalysts. The performance of obtained PtRu/WxCyOz catalysts was investigated using cyclic voltammetry, linear scan voltammetry and rotating disk electrode voltammetry. Particular attention was given to the analysis of CO poisoning, to better understand how WxCyOz species can contribute to the CO tolerance of PtRu/WxCyOz. Improved oxidation of COads at low potentials (E  LT  0.5 V vs. RHE) was ascribed to OH provided by the oxide phase at the interfacial region between the support and the PtRu particles. On the other hand, at high potentials (E > 0.5 V vs. RHE) CO removal proceeds dominantly via OH provided from the oxidized metal sites. The obtained catalyst with the best performance (30% PtRu/WxCyOz) was tested as an anode catalyst in PEM fuel cell. When using synthetic reformate as a fuel in PEMFC, there is a significant power drop of 35.3 % for the commercial 30% PtRu/C catalyst, while for the PtRu/WxCyOz anode catalyst this drop is around 16 %.
PB  - Hydrogen Energy Publications LLC
T2  - International Journal of Hydrogen Energy
T1  - Non-stoichiometric tungsten-carbide-oxide-supported Pt-Ru anode catalysts for PEM fuel cells - From basic electrochemistry to fuel cell performance
EP  - 13938
IS  - 27
SP  - 13929
VL  - 45
DO  - 10.1016/j.ijhydene.2020.03.086
UR  - conv_844
ER  - 

@article{
author = "Brković, Snežana and Marčeta-Kaninski, Milica and Lausević, Petar Z. and Šaponjić, Aleksandra B. and Radulović, Aleksandra and Rakić, Aleksandra A. and Pasti, Igor A. and Nikolić, Vladimir",
year = "2020",
abstract = "Durability and cost of Proton Exchange Membrane fuel cells (PEMFCs) are two major factors delaying their commercialization. Cost is associated with the price of the catalysts, while durability is associated with degradation and poisoning of the catalysts, primarily by CO. This motivated us to develop tungsten-carbide-oxide (WxCyOz) as a new non-carbon based catalyst support for Pt-Ru-based anode PEMFC catalyst. The aim was to improve performance and obtain higher CO tolerance compared to commercial catalysts. The performance of obtained PtRu/WxCyOz catalysts was investigated using cyclic voltammetry, linear scan voltammetry and rotating disk electrode voltammetry. Particular attention was given to the analysis of CO poisoning, to better understand how WxCyOz species can contribute to the CO tolerance of PtRu/WxCyOz. Improved oxidation of COads at low potentials (E  LT  0.5 V vs. RHE) was ascribed to OH provided by the oxide phase at the interfacial region between the support and the PtRu particles. On the other hand, at high potentials (E > 0.5 V vs. RHE) CO removal proceeds dominantly via OH provided from the oxidized metal sites. The obtained catalyst with the best performance (30% PtRu/WxCyOz) was tested as an anode catalyst in PEM fuel cell. When using synthetic reformate as a fuel in PEMFC, there is a significant power drop of 35.3 % for the commercial 30% PtRu/C catalyst, while for the PtRu/WxCyOz anode catalyst this drop is around 16 %.",
publisher = "Hydrogen Energy Publications LLC",
journal = "International Journal of Hydrogen Energy",
title = "Non-stoichiometric tungsten-carbide-oxide-supported Pt-Ru anode catalysts for PEM fuel cells - From basic electrochemistry to fuel cell performance",
pages = "13938-13929",
number = "27",
volume = "45",
doi = "10.1016/j.ijhydene.2020.03.086",
url = "conv_844"
}

Brković, S., Marčeta-Kaninski, M., Lausević, P. Z., Šaponjić, A. B., Radulović, A., Rakić, A. A., Pasti, I. A.,& Nikolić, V.. (2020). Non-stoichiometric tungsten-carbide-oxide-supported Pt-Ru anode catalysts for PEM fuel cells - From basic electrochemistry to fuel cell performance. in International Journal of Hydrogen Energy
Hydrogen Energy Publications LLC., 45(27), 13929-13938.
https://doi.org/10.1016/j.ijhydene.2020.03.086
conv_844

Brković S, Marčeta-Kaninski M, Lausević PZ, Šaponjić AB, Radulović A, Rakić AA, Pasti IA, Nikolić V. Non-stoichiometric tungsten-carbide-oxide-supported Pt-Ru anode catalysts for PEM fuel cells - From basic electrochemistry to fuel cell performance. in International Journal of Hydrogen Energy. 2020;45(27):13929-13938.
doi:10.1016/j.ijhydene.2020.03.086
conv_844 .

Brković, Snežana, Marčeta-Kaninski, Milica, Lausević, Petar Z., Šaponjić, Aleksandra B., Radulović, Aleksandra, Rakić, Aleksandra A., Pasti, Igor A., Nikolić, Vladimir, "Non-stoichiometric tungsten-carbide-oxide-supported Pt-Ru anode catalysts for PEM fuel cells - From basic electrochemistry to fuel cell performance" in International Journal of Hydrogen Energy, 45, no. 27 (2020):13929-13938,
https://doi.org/10.1016/j.ijhydene.2020.03.086 .,
conv_844 .

TY  - GEN
AU  - Rajčić, Boris
AU  - Blagojević, Stevan
AU  - Waisi, Hadi
AU  - Milovanović, Dubravka
AU  - Marinković, Miloš
AU  - Nikolić, Vladimir
AU  - Šaponjić, Zoran
AU  - Marčeta Kaninski, Milica
PY  - 2019
UR  - https://riofh.iofh.bg.ac.rs/handle/123456789/1024
T1  - ULOŽAK ZA FILTRACIONI SISTEM ZA PREČIŠĆAVANJE PIJAĆE VODE
ER  - 

@misc{
author = "Rajčić, Boris and Blagojević, Stevan and Waisi, Hadi and Milovanović, Dubravka and Marinković, Miloš and Nikolić, Vladimir and Šaponjić, Zoran and Marčeta Kaninski, Milica",
year = "2019",
title = "ULOŽAK ZA FILTRACIONI SISTEM ZA PREČIŠĆAVANJE PIJAĆE VODE"
}

Rajčić, B., Blagojević, S., Waisi, H., Milovanović, D., Marinković, M., Nikolić, V., Šaponjić, Z.,& Marčeta Kaninski, M.. (2019). ULOŽAK ZA FILTRACIONI SISTEM ZA PREČIŠĆAVANJE PIJAĆE VODE. .

Rajčić B, Blagojević S, Waisi H, Milovanović D, Marinković M, Nikolić V, Šaponjić Z, Marčeta Kaninski M. ULOŽAK ZA FILTRACIONI SISTEM ZA PREČIŠĆAVANJE PIJAĆE VODE. 2019;..

Rajčić, Boris, Blagojević, Stevan, Waisi, Hadi, Milovanović, Dubravka, Marinković, Miloš, Nikolić, Vladimir, Šaponjić, Zoran, Marčeta Kaninski, Milica, "ULOŽAK ZA FILTRACIONI SISTEM ZA PREČIŠĆAVANJE PIJAĆE VODE" (2019).

TY  - JOUR
AU  - Šaponjić, Aleksandra B.
AU  - Šaponjić, Đorđe
AU  - Perović, Ivana
AU  - Vuković, Marina
AU  - Nikolić, Vladimir
AU  - Marčeta-Kaninski, Milica
AU  - Kokunesoski, Maja
PY  - 2019
UR  - https://riofh.iofh.bg.ac.rs/handle/123456789/651
AB  - Co-Mo carbides were prepared by impregnation with aqueous solution of metal salts and sucrose into ordered mesoporous SBA-15 silica template using carbothermal hydrogen reduction. Bimetallic Co-Mo carbide obtained by using carbothermal hydrogen reduction of Co-Mo precursors is formed when the Co-Mo molar ratio is 1.0. The obtained samples were characterized by X-ray diffraction, scanning electron microscopy and energy dispersive X-ray analysis. Electrochemical characterization of obtained materials were performed by cyclic voltammetry in acid solution.
PB  - Međunarodni Institut za nauku o sinterovanju, Beograd
T2  - Science of Sintering
T1  - Synthesis and Characterization of Co-Mo Bimetallic Carbides
EP  - 326
IS  - 3
SP  - 319
VL  - 51
DO  - 10.2298/SOS1903319S
UR  - conv_827
ER  - 

@article{
author = "Šaponjić, Aleksandra B. and Šaponjić, Đorđe and Perović, Ivana and Vuković, Marina and Nikolić, Vladimir and Marčeta-Kaninski, Milica and Kokunesoski, Maja",
year = "2019",
abstract = "Co-Mo carbides were prepared by impregnation with aqueous solution of metal salts and sucrose into ordered mesoporous SBA-15 silica template using carbothermal hydrogen reduction. Bimetallic Co-Mo carbide obtained by using carbothermal hydrogen reduction of Co-Mo precursors is formed when the Co-Mo molar ratio is 1.0. The obtained samples were characterized by X-ray diffraction, scanning electron microscopy and energy dispersive X-ray analysis. Electrochemical characterization of obtained materials were performed by cyclic voltammetry in acid solution.",
publisher = "Međunarodni Institut za nauku o sinterovanju, Beograd",
journal = "Science of Sintering",
title = "Synthesis and Characterization of Co-Mo Bimetallic Carbides",
pages = "326-319",
number = "3",
volume = "51",
doi = "10.2298/SOS1903319S",
url = "conv_827"
}

Šaponjić, A. B., Šaponjić, Đ., Perović, I., Vuković, M., Nikolić, V., Marčeta-Kaninski, M.,& Kokunesoski, M.. (2019). Synthesis and Characterization of Co-Mo Bimetallic Carbides. in Science of Sintering
Međunarodni Institut za nauku o sinterovanju, Beograd., 51(3), 319-326.
https://doi.org/10.2298/SOS1903319S
conv_827

Šaponjić AB, Šaponjić Đ, Perović I, Vuković M, Nikolić V, Marčeta-Kaninski M, Kokunesoski M. Synthesis and Characterization of Co-Mo Bimetallic Carbides. in Science of Sintering. 2019;51(3):319-326.
doi:10.2298/SOS1903319S
conv_827 .

Šaponjić, Aleksandra B., Šaponjić, Đorđe, Perović, Ivana, Vuković, Marina, Nikolić, Vladimir, Marčeta-Kaninski, Milica, Kokunesoski, Maja, "Synthesis and Characterization of Co-Mo Bimetallic Carbides" in Science of Sintering, 51, no. 3 (2019):319-326,
https://doi.org/10.2298/SOS1903319S .,
conv_827 .

TY  - JOUR
AU  - Maslovara, Slađana
AU  - Vasić-Anićijević, Dragana
AU  - Brković, Snežana
AU  - Georgijević, Jelena
AU  - Tasić, Gvozden S.
AU  - Marčeta-Kaninski, Milica
PY  - 2019
UR  - https://riofh.iofh.bg.ac.rs/handle/123456789/699
AB  - In this work, nickel (Ni) cathode for hydrogen evolution reaction (HER) in alkaline medium, was modified by a combination of in situ ionic activators, based on three d-metals (Co, Cu and Mo). Catalytic performance of new Co-Cu-Mo cathode was improved compared to pure Ni in view of both increased HER reaction rate and improved energy efficiency - reduction of energy consumption of a model electrolytic cell by 15%. We discussed obtained results in comparison with previously investigated similar systems (Ni-Co-Mo and Ni-Cu-Mo). In addition, we perform a detailed surface characterization by a series of experimental techniques (XRF, XRD, SEM, profilometry and EIS) and employ DFT calculations to provide a more detailed discussion of the origin of obtained catalytic performance.
T2  - Journal of Electroanalytical Chemistry
T1  - Experimental and DFT study of CoCuMo ternary ionic activator for alkaline HER on Ni cathode
EP  - 230
SP  - 224
VL  - 839
DO  - 10.1016/j.jelechem.2019.03.044
UR  - conv_774
ER  - 

@article{
author = "Maslovara, Slađana and Vasić-Anićijević, Dragana and Brković, Snežana and Georgijević, Jelena and Tasić, Gvozden S. and Marčeta-Kaninski, Milica",
year = "2019",
abstract = "In this work, nickel (Ni) cathode for hydrogen evolution reaction (HER) in alkaline medium, was modified by a combination of in situ ionic activators, based on three d-metals (Co, Cu and Mo). Catalytic performance of new Co-Cu-Mo cathode was improved compared to pure Ni in view of both increased HER reaction rate and improved energy efficiency - reduction of energy consumption of a model electrolytic cell by 15%. We discussed obtained results in comparison with previously investigated similar systems (Ni-Co-Mo and Ni-Cu-Mo). In addition, we perform a detailed surface characterization by a series of experimental techniques (XRF, XRD, SEM, profilometry and EIS) and employ DFT calculations to provide a more detailed discussion of the origin of obtained catalytic performance.",
journal = "Journal of Electroanalytical Chemistry",
title = "Experimental and DFT study of CoCuMo ternary ionic activator for alkaline HER on Ni cathode",
pages = "230-224",
volume = "839",
doi = "10.1016/j.jelechem.2019.03.044",
url = "conv_774"
}

Maslovara, S., Vasić-Anićijević, D., Brković, S., Georgijević, J., Tasić, G. S.,& Marčeta-Kaninski, M.. (2019). Experimental and DFT study of CoCuMo ternary ionic activator for alkaline HER on Ni cathode. in Journal of Electroanalytical Chemistry, 839, 224-230.
https://doi.org/10.1016/j.jelechem.2019.03.044
conv_774

Maslovara S, Vasić-Anićijević D, Brković S, Georgijević J, Tasić GS, Marčeta-Kaninski M. Experimental and DFT study of CoCuMo ternary ionic activator for alkaline HER on Ni cathode. in Journal of Electroanalytical Chemistry. 2019;839:224-230.
doi:10.1016/j.jelechem.2019.03.044
conv_774 .

Maslovara, Slađana, Vasić-Anićijević, Dragana, Brković, Snežana, Georgijević, Jelena, Tasić, Gvozden S., Marčeta-Kaninski, Milica, "Experimental and DFT study of CoCuMo ternary ionic activator for alkaline HER on Ni cathode" in Journal of Electroanalytical Chemistry, 839 (2019):224-230,
https://doi.org/10.1016/j.jelechem.2019.03.044 .,
conv_774 .

TY  - JOUR
AU  - Brković, Snežana
AU  - Nikolić, Vladimir
AU  - Marčeta-Kaninski, Milica
AU  - Pasti, Igor A.
PY  - 2019
UR  - https://riofh.iofh.bg.ac.rs/handle/123456789/658
AB  - Hydrogen Oxidation Reaction (HOR) is anode reaction in Proton exchange membrane fuel cells (PEMFCs) and it has very fast kinetics. However, the purity of fuel (H-2) is very important and can slow down HOR kinetics, affecting the overall PEMFC performance. The performance of commercial Pt/C catalyst impregnated with WOx, as a catalyst for HOR, was investigated using a set of electrochemical methods (cyclic voltammetry, linear scan voltammetry and rotating disk electrode voltammetry). In order to deepen the understanding how WOx, species can contribute CO tolerance of Pt/C, a particular attention was paid to CO poisoning. In the absence of CO, HOR is under diffusion limitations and HOR kinetics is not affected by WOx species. Appreciable HOR current on the electrodes pre-saturated with COads at potentials above 0.3 V vs. RHE, which is not observed for pure Pt/C, was discussed in details. HOR liming diffusion currents for higher concentrations of W are reached at high anodic potentials. The obtained results were explained by donation of OHads by WOx phase for COads removal in the mid potential region and reduced reactivity of Pt surface sites in the vicinity of the Pt vertical bar WOx, interface. The obtained results can provide guidelines for development of novel CO tolerant PEMFC anode catalysts.
T2  - International Journal of Hydrogen Energy
T1  - Pt/C catalyst impregnated with tungsten-oxide - Hydrogen oxidation reaction vs. CO tolerance
EP  - 13372
IS  - 26
SP  - 13364
VL  - 44
DO  - 10.1016/j.ijhydene.2019.03.270
UR  - conv_778
ER  - 

@article{
author = "Brković, Snežana and Nikolić, Vladimir and Marčeta-Kaninski, Milica and Pasti, Igor A.",
year = "2019",
abstract = "Hydrogen Oxidation Reaction (HOR) is anode reaction in Proton exchange membrane fuel cells (PEMFCs) and it has very fast kinetics. However, the purity of fuel (H-2) is very important and can slow down HOR kinetics, affecting the overall PEMFC performance. The performance of commercial Pt/C catalyst impregnated with WOx, as a catalyst for HOR, was investigated using a set of electrochemical methods (cyclic voltammetry, linear scan voltammetry and rotating disk electrode voltammetry). In order to deepen the understanding how WOx, species can contribute CO tolerance of Pt/C, a particular attention was paid to CO poisoning. In the absence of CO, HOR is under diffusion limitations and HOR kinetics is not affected by WOx species. Appreciable HOR current on the electrodes pre-saturated with COads at potentials above 0.3 V vs. RHE, which is not observed for pure Pt/C, was discussed in details. HOR liming diffusion currents for higher concentrations of W are reached at high anodic potentials. The obtained results were explained by donation of OHads by WOx phase for COads removal in the mid potential region and reduced reactivity of Pt surface sites in the vicinity of the Pt vertical bar WOx, interface. The obtained results can provide guidelines for development of novel CO tolerant PEMFC anode catalysts.",
journal = "International Journal of Hydrogen Energy",
title = "Pt/C catalyst impregnated with tungsten-oxide - Hydrogen oxidation reaction vs. CO tolerance",
pages = "13372-13364",
number = "26",
volume = "44",
doi = "10.1016/j.ijhydene.2019.03.270",
url = "conv_778"
}

Brković, S., Nikolić, V., Marčeta-Kaninski, M.,& Pasti, I. A.. (2019). Pt/C catalyst impregnated with tungsten-oxide - Hydrogen oxidation reaction vs. CO tolerance. in International Journal of Hydrogen Energy, 44(26), 13364-13372.
https://doi.org/10.1016/j.ijhydene.2019.03.270
conv_778

Brković S, Nikolić V, Marčeta-Kaninski M, Pasti IA. Pt/C catalyst impregnated with tungsten-oxide - Hydrogen oxidation reaction vs. CO tolerance. in International Journal of Hydrogen Energy. 2019;44(26):13364-13372.
doi:10.1016/j.ijhydene.2019.03.270
conv_778 .

Brković, Snežana, Nikolić, Vladimir, Marčeta-Kaninski, Milica, Pasti, Igor A., "Pt/C catalyst impregnated with tungsten-oxide - Hydrogen oxidation reaction vs. CO tolerance" in International Journal of Hydrogen Energy, 44, no. 26 (2019):13364-13372,
https://doi.org/10.1016/j.ijhydene.2019.03.270 .,
conv_778 .

TY  - JOUR
AU  - Maslovara, Slađana
AU  - Vasić-Anićijević, Dragana
AU  - Kijevčanin, Mirjana
AU  - Radović, Ivona R.
AU  - Nikolić, Vladimir
AU  - Lausević, Petar Z.
AU  - Marčeta-Kaninski, Milica
PY  - 2017
UR  - https://riofh.iofh.bg.ac.rs/handle/123456789/566
AB  - In this paper we discussed various factors contributing to the improvement of hydrogen evolution reaction (HER) activity of Ni and stainless steel electrodes activated by in situ addition of NiCoMo activators, using a combination of experimental techniques and DFT calculations. By comparing energy consumption of stainless steel (SS) electrodes in a lab scale alkaline electrolyzer with and without ionic activation, we obtained reduction of energy consumption by 21% at industrial conditions (high current density and temperature). We recorded U-I curves for activated and non-activated stainless steel electrodes in the current density range from 40 to 500 mA cm(2) and in the temperature range 298-343 K, and the obtained results were used in an electrochemical model of the laboratory alkaline electrolyzer. Increase of the electrode surface upon addition of ionic activators was confirmed by profilometric measurements and SEM analysis. Finally, we applied density functional theory (DFT) to discuss partial roles of applied ionic activators (Ni, Co and Mo) in the modification and improvement of the intrinsic properties of the cathode towards the HER in alkaline medium. From the combination of profilometric, SEM and DFT results, we conclude that the main factor contributing to the improvement of HER activity of Ni electrodes upon NiCoMo activation is the increase of electrode surface area.
T2  - International Journal of Hydrogen Energy
T1  - Improved HER activity of Ni and stainless steel electrodes activated by NiCoMo ionic activator - A combined DFT and experimental study
EP  - 5082
IS  - 8
SP  - 5072
VL  - 42
DO  - 10.1016/j.ijhydene.2016.12.116
UR  - conv_665
ER  - 

@article{
author = "Maslovara, Slađana and Vasić-Anićijević, Dragana and Kijevčanin, Mirjana and Radović, Ivona R. and Nikolić, Vladimir and Lausević, Petar Z. and Marčeta-Kaninski, Milica",
year = "2017",
abstract = "In this paper we discussed various factors contributing to the improvement of hydrogen evolution reaction (HER) activity of Ni and stainless steel electrodes activated by in situ addition of NiCoMo activators, using a combination of experimental techniques and DFT calculations. By comparing energy consumption of stainless steel (SS) electrodes in a lab scale alkaline electrolyzer with and without ionic activation, we obtained reduction of energy consumption by 21% at industrial conditions (high current density and temperature). We recorded U-I curves for activated and non-activated stainless steel electrodes in the current density range from 40 to 500 mA cm(2) and in the temperature range 298-343 K, and the obtained results were used in an electrochemical model of the laboratory alkaline electrolyzer. Increase of the electrode surface upon addition of ionic activators was confirmed by profilometric measurements and SEM analysis. Finally, we applied density functional theory (DFT) to discuss partial roles of applied ionic activators (Ni, Co and Mo) in the modification and improvement of the intrinsic properties of the cathode towards the HER in alkaline medium. From the combination of profilometric, SEM and DFT results, we conclude that the main factor contributing to the improvement of HER activity of Ni electrodes upon NiCoMo activation is the increase of electrode surface area.",
journal = "International Journal of Hydrogen Energy",
title = "Improved HER activity of Ni and stainless steel electrodes activated by NiCoMo ionic activator - A combined DFT and experimental study",
pages = "5082-5072",
number = "8",
volume = "42",
doi = "10.1016/j.ijhydene.2016.12.116",
url = "conv_665"
}

Maslovara, S., Vasić-Anićijević, D., Kijevčanin, M., Radović, I. R., Nikolić, V., Lausević, P. Z.,& Marčeta-Kaninski, M.. (2017). Improved HER activity of Ni and stainless steel electrodes activated by NiCoMo ionic activator - A combined DFT and experimental study. in International Journal of Hydrogen Energy, 42(8), 5072-5082.
https://doi.org/10.1016/j.ijhydene.2016.12.116
conv_665

Maslovara S, Vasić-Anićijević D, Kijevčanin M, Radović IR, Nikolić V, Lausević PZ, Marčeta-Kaninski M. Improved HER activity of Ni and stainless steel electrodes activated by NiCoMo ionic activator - A combined DFT and experimental study. in International Journal of Hydrogen Energy. 2017;42(8):5072-5082.
doi:10.1016/j.ijhydene.2016.12.116
conv_665 .

Maslovara, Slađana, Vasić-Anićijević, Dragana, Kijevčanin, Mirjana, Radović, Ivona R., Nikolić, Vladimir, Lausević, Petar Z., Marčeta-Kaninski, Milica, "Improved HER activity of Ni and stainless steel electrodes activated by NiCoMo ionic activator - A combined DFT and experimental study" in International Journal of Hydrogen Energy, 42, no. 8 (2017):5072-5082,
https://doi.org/10.1016/j.ijhydene.2016.12.116 .,
conv_665 .

TY  - JOUR
AU  - Nikolić, Vladimir
AU  - Karić, Slavko D.
AU  - Nikolić, Željka
AU  - Tošić, Miloš
AU  - Tasić, Gvozden S.
AU  - Milovanović, Dubravka
AU  - Marčeta-Kaninski, Milica
PY  - 2017
UR  - https://riofh.iofh.bg.ac.rs/handle/123456789/546
AB  - Polycyclic aromatic hydrocarbons (PAHs) are denoted by International Agency for Research on Cancer as mutagens, teratogens and carcinogenic to humans. In 2013, Vinca Institute of Nuclear Sciences was hired to determine whether PAHs are present in significant quantities in the concrete walls of newly built residential buildings (about 15,000 m(2) of apartments), and to propose appropriate technical solution for PAH removal in this case. As PAH occurrence, determination and remediation in concrete is, to our knowledge, a completely new field, it was necessary to face a number of challenges, including lack of regulations considering contents of PAHs in concrete, investigation of the origin of PAH contamination in concrete (if established), as Well as finding feasible and non-expensive remediation method, which would be appropriate for residential space. In first part of this study, a Markedly high concentrations of 5 PAHs were detected by UPLC/PDA analysis in samples of both concrete walls and mineral oil used for coating of planks during formwork, while control concrete and mineral oil, taken from independent construction site, were taken as a reference. Such coincidence, as well as the fact that mineral oil has penetrated into the concrete which is proven by ASAP/MS analysis, pointed to the mineral oil as the most probable source of PAH contamination of the concrete. In the second part, an efficient and easy-applicable method for PAH oxidation in concrete (called FHO3AOP), using UV light, H2O2 and ozone, was presented and discussed in terms of previous literature data.
T2  - Chemical Engineering Journal
T1  - Novel photochemical advanced oxidation process for the removal of polycyclic aromatic hydrocarbons from polluted concrete
EP  - 105
SP  - 99
VL  - 312
DO  - 10.1016/j.cej.2016.11.117
UR  - conv_645
ER  - 

@article{
author = "Nikolić, Vladimir and Karić, Slavko D. and Nikolić, Željka and Tošić, Miloš and Tasić, Gvozden S. and Milovanović, Dubravka and Marčeta-Kaninski, Milica",
year = "2017",
abstract = "Polycyclic aromatic hydrocarbons (PAHs) are denoted by International Agency for Research on Cancer as mutagens, teratogens and carcinogenic to humans. In 2013, Vinca Institute of Nuclear Sciences was hired to determine whether PAHs are present in significant quantities in the concrete walls of newly built residential buildings (about 15,000 m(2) of apartments), and to propose appropriate technical solution for PAH removal in this case. As PAH occurrence, determination and remediation in concrete is, to our knowledge, a completely new field, it was necessary to face a number of challenges, including lack of regulations considering contents of PAHs in concrete, investigation of the origin of PAH contamination in concrete (if established), as Well as finding feasible and non-expensive remediation method, which would be appropriate for residential space. In first part of this study, a Markedly high concentrations of 5 PAHs were detected by UPLC/PDA analysis in samples of both concrete walls and mineral oil used for coating of planks during formwork, while control concrete and mineral oil, taken from independent construction site, were taken as a reference. Such coincidence, as well as the fact that mineral oil has penetrated into the concrete which is proven by ASAP/MS analysis, pointed to the mineral oil as the most probable source of PAH contamination of the concrete. In the second part, an efficient and easy-applicable method for PAH oxidation in concrete (called FHO3AOP), using UV light, H2O2 and ozone, was presented and discussed in terms of previous literature data.",
journal = "Chemical Engineering Journal",
title = "Novel photochemical advanced oxidation process for the removal of polycyclic aromatic hydrocarbons from polluted concrete",
pages = "105-99",
volume = "312",
doi = "10.1016/j.cej.2016.11.117",
url = "conv_645"
}

Nikolić, V., Karić, S. D., Nikolić, Ž., Tošić, M., Tasić, G. S., Milovanović, D.,& Marčeta-Kaninski, M.. (2017). Novel photochemical advanced oxidation process for the removal of polycyclic aromatic hydrocarbons from polluted concrete. in Chemical Engineering Journal, 312, 99-105.
https://doi.org/10.1016/j.cej.2016.11.117
conv_645

Nikolić V, Karić SD, Nikolić Ž, Tošić M, Tasić GS, Milovanović D, Marčeta-Kaninski M. Novel photochemical advanced oxidation process for the removal of polycyclic aromatic hydrocarbons from polluted concrete. in Chemical Engineering Journal. 2017;312:99-105.
doi:10.1016/j.cej.2016.11.117
conv_645 .

Nikolić, Vladimir, Karić, Slavko D., Nikolić, Željka, Tošić, Miloš, Tasić, Gvozden S., Milovanović, Dubravka, Marčeta-Kaninski, Milica, "Novel photochemical advanced oxidation process for the removal of polycyclic aromatic hydrocarbons from polluted concrete" in Chemical Engineering Journal, 312 (2017):99-105,
https://doi.org/10.1016/j.cej.2016.11.117 .,
conv_645 .

TY  - JOUR
AU  - Aćimović, Danka D.
AU  - Karić, Slavko D.
AU  - Nikolić, Željka
AU  - Brdarić, Tanja P.
AU  - Tasić, Gvozden S.
AU  - Marčeta-Kaninski, Milica
AU  - Nikolić, Vladimir
PY  - 2017
UR  - https://riofh.iofh.bg.ac.rs/handle/123456789/540
AB  - Polycyclic aromatic hydrocarbons (PAH) have been listed by the United States Environmental Protection Agency (US EPA) and by the European Community as priority environmental pollutants. The removal of PAHs from soils, sediments and waste water has attracted attention of scientists and engineers for several decades. Electrochemical oxidation of PAH compounds in water, is receiving increasing attention, due to its convenience and simplicity. In this study we performed electrochemical oxidation of 16 EPA PAHs mixture in 10% NaCI aqueous solution in potentiostatic conditions, at voltage 1 V. Decrease of concentration of some individual PAHs, up to 70% referred to their starting concentration, after 60 min of electrolysis, was confirmed by UPLC/PDA analysis. In further work investigation was extrapolated to in situ removal of PAHs from concrete, as the medium where, to our knowledge, such way of PAH removal has not been investigated before. High concentrations of PAH contamination occurred in the concrete structure of the residential buildings in Belgrade in 2014. Application of DC voltage of 50 V between nickel and stainless steel electrodes packed in the concrete wall, moisturized with the 10% NaCI solution, led to considerable removal of the pollutants by oxidation process throughout the concrete.
PB  - Elsevier Ltd.
T2  - Environmental Pollution
T1  - Electrochemical oxidation of the polycyclic aromatic hydrocarbons in polluted concrete of the residential buildings
EP  - 399
SP  - 393
VL  - 220
DO  - 10.1016/j.envpol.2016.09.075
UR  - conv_639
ER  - 

@article{
author = "Aćimović, Danka D. and Karić, Slavko D. and Nikolić, Željka and Brdarić, Tanja P. and Tasić, Gvozden S. and Marčeta-Kaninski, Milica and Nikolić, Vladimir",
year = "2017",
abstract = "Polycyclic aromatic hydrocarbons (PAH) have been listed by the United States Environmental Protection Agency (US EPA) and by the European Community as priority environmental pollutants. The removal of PAHs from soils, sediments and waste water has attracted attention of scientists and engineers for several decades. Electrochemical oxidation of PAH compounds in water, is receiving increasing attention, due to its convenience and simplicity. In this study we performed electrochemical oxidation of 16 EPA PAHs mixture in 10% NaCI aqueous solution in potentiostatic conditions, at voltage 1 V. Decrease of concentration of some individual PAHs, up to 70% referred to their starting concentration, after 60 min of electrolysis, was confirmed by UPLC/PDA analysis. In further work investigation was extrapolated to in situ removal of PAHs from concrete, as the medium where, to our knowledge, such way of PAH removal has not been investigated before. High concentrations of PAH contamination occurred in the concrete structure of the residential buildings in Belgrade in 2014. Application of DC voltage of 50 V between nickel and stainless steel electrodes packed in the concrete wall, moisturized with the 10% NaCI solution, led to considerable removal of the pollutants by oxidation process throughout the concrete.",
publisher = "Elsevier Ltd.",
journal = "Environmental Pollution",
title = "Electrochemical oxidation of the polycyclic aromatic hydrocarbons in polluted concrete of the residential buildings",
pages = "399-393",
volume = "220",
doi = "10.1016/j.envpol.2016.09.075",
url = "conv_639"
}

Aćimović, D. D., Karić, S. D., Nikolić, Ž., Brdarić, T. P., Tasić, G. S., Marčeta-Kaninski, M.,& Nikolić, V.. (2017). Electrochemical oxidation of the polycyclic aromatic hydrocarbons in polluted concrete of the residential buildings. in Environmental Pollution
Elsevier Ltd.., 220, 393-399.
https://doi.org/10.1016/j.envpol.2016.09.075
conv_639

Aćimović DD, Karić SD, Nikolić Ž, Brdarić TP, Tasić GS, Marčeta-Kaninski M, Nikolić V. Electrochemical oxidation of the polycyclic aromatic hydrocarbons in polluted concrete of the residential buildings. in Environmental Pollution. 2017;220:393-399.
doi:10.1016/j.envpol.2016.09.075
conv_639 .

Aćimović, Danka D., Karić, Slavko D., Nikolić, Željka, Brdarić, Tanja P., Tasić, Gvozden S., Marčeta-Kaninski, Milica, Nikolić, Vladimir, "Electrochemical oxidation of the polycyclic aromatic hydrocarbons in polluted concrete of the residential buildings" in Environmental Pollution, 220 (2017):393-399,
https://doi.org/10.1016/j.envpol.2016.09.075 .,
conv_639 .

TY  - JOUR
AU  - Aćimović, Danka D.
AU  - Nikolić, Željka
AU  - Tošić, Miloš
AU  - Milovanović, Dubravka
AU  - Nikolić, Vladimir
AU  - Brdarić, Tanja P.
AU  - Marčeta-Kaninski, Milica
PY  - 2017
UR  - https://riofh.iofh.bg.ac.rs/handle/123456789/531
AB  - Human exposure to persistent organic contaminants, from building materials, negatively affects people's health and overall quality of life. This paper presents the validation and uncertainty assessment of the analytical method, developed for the simultaneous determination of 16 EPA polycyclic aromatic hydrocarbons (PAHs) in solid-solid concrete by ultra-performance liquid chromatography with photo diode-array detector. Linearity of calibration curves was good over the whole range of calibration. Limits of detection varied between 0.2 and 2.9 mu gkg(-1). The accuracy in terms of recovery of the validated method is within the range from 54 to 106%. The developed method proved to be appropriate for analysis of PAHs and can be used for the quality control testing of concrete during the construction of new buildings, the old residences and related buildings associated with sick-building syndrome. In addition, this is the first reported method described for the evaluation of PAHs in solid-solid concrete.
T2  - Journal of Hazardous Materials
T1  - Validation and uncertainty estimation of UPLC-PDA method for the analysis of polycyclic aromatic hydrocarbons in concrete
EP  - 278
SP  - 271
VL  - 325
DO  - 10.1016/j.jhazmat.2016.12.008
UR  - conv_642
ER  - 

@article{
author = "Aćimović, Danka D. and Nikolić, Željka and Tošić, Miloš and Milovanović, Dubravka and Nikolić, Vladimir and Brdarić, Tanja P. and Marčeta-Kaninski, Milica",
year = "2017",
abstract = "Human exposure to persistent organic contaminants, from building materials, negatively affects people's health and overall quality of life. This paper presents the validation and uncertainty assessment of the analytical method, developed for the simultaneous determination of 16 EPA polycyclic aromatic hydrocarbons (PAHs) in solid-solid concrete by ultra-performance liquid chromatography with photo diode-array detector. Linearity of calibration curves was good over the whole range of calibration. Limits of detection varied between 0.2 and 2.9 mu gkg(-1). The accuracy in terms of recovery of the validated method is within the range from 54 to 106%. The developed method proved to be appropriate for analysis of PAHs and can be used for the quality control testing of concrete during the construction of new buildings, the old residences and related buildings associated with sick-building syndrome. In addition, this is the first reported method described for the evaluation of PAHs in solid-solid concrete.",
journal = "Journal of Hazardous Materials",
title = "Validation and uncertainty estimation of UPLC-PDA method for the analysis of polycyclic aromatic hydrocarbons in concrete",
pages = "278-271",
volume = "325",
doi = "10.1016/j.jhazmat.2016.12.008",
url = "conv_642"
}

Aćimović, D. D., Nikolić, Ž., Tošić, M., Milovanović, D., Nikolić, V., Brdarić, T. P.,& Marčeta-Kaninski, M.. (2017). Validation and uncertainty estimation of UPLC-PDA method for the analysis of polycyclic aromatic hydrocarbons in concrete. in Journal of Hazardous Materials, 325, 271-278.
https://doi.org/10.1016/j.jhazmat.2016.12.008
conv_642

Aćimović DD, Nikolić Ž, Tošić M, Milovanović D, Nikolić V, Brdarić TP, Marčeta-Kaninski M. Validation and uncertainty estimation of UPLC-PDA method for the analysis of polycyclic aromatic hydrocarbons in concrete. in Journal of Hazardous Materials. 2017;325:271-278.
doi:10.1016/j.jhazmat.2016.12.008
conv_642 .

Aćimović, Danka D., Nikolić, Željka, Tošić, Miloš, Milovanović, Dubravka, Nikolić, Vladimir, Brdarić, Tanja P., Marčeta-Kaninski, Milica, "Validation and uncertainty estimation of UPLC-PDA method for the analysis of polycyclic aromatic hydrocarbons in concrete" in Journal of Hazardous Materials, 325 (2017):271-278,
https://doi.org/10.1016/j.jhazmat.2016.12.008 .,
conv_642 .

TY  - JOUR
AU  - Vasić-Anićijević, Dragana
AU  - Perović, Ivana M.
AU  - Maslovara, Slađana
AU  - Brković, Snežana
AU  - Zugić, Dragana L.
AU  - Lausević, Zoran V.
AU  - Marčeta-Kaninski, Milica
PY  - 2016
UR  - https://riofh.iofh.bg.ac.rs/handle/123456789/475
AB  - A systematic ab initio (DFT-GGA) study of adsorption of various oxygen species on graphene has been performed in order to find out general trends and provide a good starting point to analyze the oxidation of more complex carbon materials. Particular attention was paid to finding an appropriate supercell model. According to our findings, atomic O is characterized by stable adsorption on graphene and very strong adsorption on defective graphene. On the other hand, O-2 does not adsorb on graphene and is allowed to diffuse freely to the defect, where it is expected to dissociate into two strongly adsorbed O atoms. The obtained results were compared with available theoretical data in the literature and good agreement was achieved.
PB  - Society of Chemists and Technologists of Macedonia
T2  - Macedonian Journal of Chemistry and Chemical Engineering
T1  - Ab initio study of graphene interaction with o-2, o, and o-
EP  - 274
IS  - 2
SP  - 271
VL  - 35
DO  - 10.20450/mjcce.2016.1038
UR  - conv_646
ER  - 

@article{
author = "Vasić-Anićijević, Dragana and Perović, Ivana M. and Maslovara, Slađana and Brković, Snežana and Zugić, Dragana L. and Lausević, Zoran V. and Marčeta-Kaninski, Milica",
year = "2016",
abstract = "A systematic ab initio (DFT-GGA) study of adsorption of various oxygen species on graphene has been performed in order to find out general trends and provide a good starting point to analyze the oxidation of more complex carbon materials. Particular attention was paid to finding an appropriate supercell model. According to our findings, atomic O is characterized by stable adsorption on graphene and very strong adsorption on defective graphene. On the other hand, O-2 does not adsorb on graphene and is allowed to diffuse freely to the defect, where it is expected to dissociate into two strongly adsorbed O atoms. The obtained results were compared with available theoretical data in the literature and good agreement was achieved.",
publisher = "Society of Chemists and Technologists of Macedonia",
journal = "Macedonian Journal of Chemistry and Chemical Engineering",
title = "Ab initio study of graphene interaction with o-2, o, and o-",
pages = "274-271",
number = "2",
volume = "35",
doi = "10.20450/mjcce.2016.1038",
url = "conv_646"
}

Vasić-Anićijević, D., Perović, I. M., Maslovara, S., Brković, S., Zugić, D. L., Lausević, Z. V.,& Marčeta-Kaninski, M.. (2016). Ab initio study of graphene interaction with o-2, o, and o-. in Macedonian Journal of Chemistry and Chemical Engineering
Society of Chemists and Technologists of Macedonia., 35(2), 271-274.
https://doi.org/10.20450/mjcce.2016.1038
conv_646

Vasić-Anićijević D, Perović IM, Maslovara S, Brković S, Zugić DL, Lausević ZV, Marčeta-Kaninski M. Ab initio study of graphene interaction with o-2, o, and o-. in Macedonian Journal of Chemistry and Chemical Engineering. 2016;35(2):271-274.
doi:10.20450/mjcce.2016.1038
conv_646 .

Vasić-Anićijević, Dragana, Perović, Ivana M., Maslovara, Slađana, Brković, Snežana, Zugić, Dragana L., Lausević, Zoran V., Marčeta-Kaninski, Milica, "Ab initio study of graphene interaction with o-2, o, and o-" in Macedonian Journal of Chemistry and Chemical Engineering, 35, no. 2 (2016):271-274,
https://doi.org/10.20450/mjcce.2016.1038 .,
conv_646 .

TY  - JOUR
AU  - Miulović, Snežana M.
AU  - Nikolić, Vladimir
AU  - Lausević, Petar Z.
AU  - Aćimović, Danka D.
AU  - Tasić, Gvozden S.
AU  - Marčeta-Kaninski, Milica
PY  - 2015
UR  - https://riofh.iofh.bg.ac.rs/handle/123456789/384
AB  - The electrochemical behavior of cobalt ethylenediamine complexes (Co(en)), at pH 12 was investigated by cyclic voltammetry (CV), the potentiostatic pulse technique and polarization curve measurements at stationary and rotating glassy carbon (GC) electrodes. It was shown that sixteen different species could be formed in a solution containing Co(en)3, with the most stable one at all pH values being [Co(en)(3)](3+). The reduction of [Co(en)(3)](3+) into [Co(en)(3)](2+) was shown to be a totally irreversible, one-electron exchange reaction. Further reduction of [Co(en)(3)](2+) was found to be a complex process leading to cobalt deposition at potentials more negative than -1.45 V vs. SCE. The process of [Co(en)(3)](2+) oxidation was also complex and most probably coupled with chemical reactions.
PB  - Srpsko hemijsko društvo, Beograd
T2  - Journal of the Serbian Chemical Society
T1  - Electrochemistry of cobalt ethylenediamine complexes at high pH
EP  - 1527
IS  - 12
SP  - 1515
VL  - 80
DO  - 10.2298/JSC150327079M
UR  - conv_586
ER  - 

@article{
author = "Miulović, Snežana M. and Nikolić, Vladimir and Lausević, Petar Z. and Aćimović, Danka D. and Tasić, Gvozden S. and Marčeta-Kaninski, Milica",
year = "2015",
abstract = "The electrochemical behavior of cobalt ethylenediamine complexes (Co(en)), at pH 12 was investigated by cyclic voltammetry (CV), the potentiostatic pulse technique and polarization curve measurements at stationary and rotating glassy carbon (GC) electrodes. It was shown that sixteen different species could be formed in a solution containing Co(en)3, with the most stable one at all pH values being [Co(en)(3)](3+). The reduction of [Co(en)(3)](3+) into [Co(en)(3)](2+) was shown to be a totally irreversible, one-electron exchange reaction. Further reduction of [Co(en)(3)](2+) was found to be a complex process leading to cobalt deposition at potentials more negative than -1.45 V vs. SCE. The process of [Co(en)(3)](2+) oxidation was also complex and most probably coupled with chemical reactions.",
publisher = "Srpsko hemijsko društvo, Beograd",
journal = "Journal of the Serbian Chemical Society",
title = "Electrochemistry of cobalt ethylenediamine complexes at high pH",
pages = "1527-1515",
number = "12",
volume = "80",
doi = "10.2298/JSC150327079M",
url = "conv_586"
}

Miulović, S. M., Nikolić, V., Lausević, P. Z., Aćimović, D. D., Tasić, G. S.,& Marčeta-Kaninski, M.. (2015). Electrochemistry of cobalt ethylenediamine complexes at high pH. in Journal of the Serbian Chemical Society
Srpsko hemijsko društvo, Beograd., 80(12), 1515-1527.
https://doi.org/10.2298/JSC150327079M
conv_586

Miulović SM, Nikolić V, Lausević PZ, Aćimović DD, Tasić GS, Marčeta-Kaninski M. Electrochemistry of cobalt ethylenediamine complexes at high pH. in Journal of the Serbian Chemical Society. 2015;80(12):1515-1527.
doi:10.2298/JSC150327079M
conv_586 .

Miulović, Snežana M., Nikolić, Vladimir, Lausević, Petar Z., Aćimović, Danka D., Tasić, Gvozden S., Marčeta-Kaninski, Milica, "Electrochemistry of cobalt ethylenediamine complexes at high pH" in Journal of the Serbian Chemical Society, 80, no. 12 (2015):1515-1527,
https://doi.org/10.2298/JSC150327079M .,
conv_586 .

TY  - JOUR
AU  - Nikolić, Vladimir
AU  - Maslovara, Slađana
AU  - Tasić, Gvozden S.
AU  - Brdarić, Tanja P.
AU  - Lausević, Petar Z.
AU  - Radak, Bojan B.
AU  - Marčeta-Kaninski, Milica
PY  - 2015
UR  - https://riofh.iofh.bg.ac.rs/handle/123456789/377
AB  - This paper presents investigations on the influence of in-situ ionic activation using combination of three D-metals: Ni, Co and Moon the hydrogen evolution reaction (HER) mechanism and kinetics. Polarization measurements were performed to obtain kinetic parameters for the HER and the results are presented to show Tafel slopes, exchange current densities and apparent energy of activation. The values of the kinetic parameters confirm the existence of two Tafel slopes, in the case of NiCoMo based ionic activators (i.a.) in the investigated temperature range, with very high values of the exchange current density. Electrochemical impedance spectroscopy measurements were employed to further investigate the origin of the obtained electrocatalytic effect on the HER. The measurements were performed at several overpotentials and temperatures. It was found that co-deposition of Ni, Co and Mo species on the Ni cathode results in a large number of active sites for hydrogen adsorption, and a synergetic effect giving electronic structure suitable for the HER, are the main factors contributing to the enhanced HER kinetics. It was shown that EIS measurements had a crucial role in determining the HER mechanism, especially with the complex in-situ activation of the alkaline electrolysis.
T2  - Applied Catalysis B-Environmental
T1  - Kinetics of hydrogen evolution reaction in alkaline electrolysis on a Ni cathode in the presence of Ni-Co-Mo based ionic activators
EP  - 94
SP  - 88
VL  - 179
DO  - 10.1016/j.apcatb.2015.05.012
UR  - conv_561
ER  - 

@article{
author = "Nikolić, Vladimir and Maslovara, Slađana and Tasić, Gvozden S. and Brdarić, Tanja P. and Lausević, Petar Z. and Radak, Bojan B. and Marčeta-Kaninski, Milica",
year = "2015",
abstract = "This paper presents investigations on the influence of in-situ ionic activation using combination of three D-metals: Ni, Co and Moon the hydrogen evolution reaction (HER) mechanism and kinetics. Polarization measurements were performed to obtain kinetic parameters for the HER and the results are presented to show Tafel slopes, exchange current densities and apparent energy of activation. The values of the kinetic parameters confirm the existence of two Tafel slopes, in the case of NiCoMo based ionic activators (i.a.) in the investigated temperature range, with very high values of the exchange current density. Electrochemical impedance spectroscopy measurements were employed to further investigate the origin of the obtained electrocatalytic effect on the HER. The measurements were performed at several overpotentials and temperatures. It was found that co-deposition of Ni, Co and Mo species on the Ni cathode results in a large number of active sites for hydrogen adsorption, and a synergetic effect giving electronic structure suitable for the HER, are the main factors contributing to the enhanced HER kinetics. It was shown that EIS measurements had a crucial role in determining the HER mechanism, especially with the complex in-situ activation of the alkaline electrolysis.",
journal = "Applied Catalysis B-Environmental",
title = "Kinetics of hydrogen evolution reaction in alkaline electrolysis on a Ni cathode in the presence of Ni-Co-Mo based ionic activators",
pages = "94-88",
volume = "179",
doi = "10.1016/j.apcatb.2015.05.012",
url = "conv_561"
}

Nikolić, V., Maslovara, S., Tasić, G. S., Brdarić, T. P., Lausević, P. Z., Radak, B. B.,& Marčeta-Kaninski, M.. (2015). Kinetics of hydrogen evolution reaction in alkaline electrolysis on a Ni cathode in the presence of Ni-Co-Mo based ionic activators. in Applied Catalysis B-Environmental, 179, 88-94.
https://doi.org/10.1016/j.apcatb.2015.05.012
conv_561

Nikolić V, Maslovara S, Tasić GS, Brdarić TP, Lausević PZ, Radak BB, Marčeta-Kaninski M. Kinetics of hydrogen evolution reaction in alkaline electrolysis on a Ni cathode in the presence of Ni-Co-Mo based ionic activators. in Applied Catalysis B-Environmental. 2015;179:88-94.
doi:10.1016/j.apcatb.2015.05.012
conv_561 .

Nikolić, Vladimir, Maslovara, Slađana, Tasić, Gvozden S., Brdarić, Tanja P., Lausević, Petar Z., Radak, Bojan B., Marčeta-Kaninski, Milica, "Kinetics of hydrogen evolution reaction in alkaline electrolysis on a Ni cathode in the presence of Ni-Co-Mo based ionic activators" in Applied Catalysis B-Environmental, 179 (2015):88-94,
https://doi.org/10.1016/j.apcatb.2015.05.012 .,
conv_561 .

TY  - JOUR
AU  - Perović, Nana M.
AU  - Aćimović, Danka D.
AU  - Tasić, Gvozden S.
AU  - Karić, Slavko D.
AU  - Lausević, Petar Z.
AU  - Marčeta-Kaninski, Milica
AU  - Nikolić, Vladimir
PY  - 2015
UR  - https://riofh.iofh.bg.ac.rs/handle/123456789/371
AB  - This manuscript presents contribution on the improved efficiency of the alkaline electrolytic production of hydrogen by in situ adding activating compounds directly into the electrolyte during the electrolytic process. New electrode material, ternary system, Ni-Cu-Mo, was applied as activating compound i.e. ionic activator. The energy requirements per mass unit of hydrogen produced is reduced for more than 10%, compared to non-activated, 30 wt. % KOH electrolyte system. Energy saving is higher at higher temperatures and at higher current densities. During the electrolytic process, the ionic activators develop nanosized porous structure deposits on the surface of the Ni electrode. Presented results point out a strong possibility of the usage of ternary ionic activators in industrial applications.
T2  - International Journal of Hydrogen Energy
T1  - Efficient hydrogen production using ternary Ni-Cu-Mo ionic activator
EP  - 6275
IS  - 19
SP  - 6270
VL  - 40
DO  - 10.1016/j.ijhydene.2015.03.003
UR  - conv_547
ER  - 

@article{
author = "Perović, Nana M. and Aćimović, Danka D. and Tasić, Gvozden S. and Karić, Slavko D. and Lausević, Petar Z. and Marčeta-Kaninski, Milica and Nikolić, Vladimir",
year = "2015",
abstract = "This manuscript presents contribution on the improved efficiency of the alkaline electrolytic production of hydrogen by in situ adding activating compounds directly into the electrolyte during the electrolytic process. New electrode material, ternary system, Ni-Cu-Mo, was applied as activating compound i.e. ionic activator. The energy requirements per mass unit of hydrogen produced is reduced for more than 10%, compared to non-activated, 30 wt. % KOH electrolyte system. Energy saving is higher at higher temperatures and at higher current densities. During the electrolytic process, the ionic activators develop nanosized porous structure deposits on the surface of the Ni electrode. Presented results point out a strong possibility of the usage of ternary ionic activators in industrial applications.",
journal = "International Journal of Hydrogen Energy",
title = "Efficient hydrogen production using ternary Ni-Cu-Mo ionic activator",
pages = "6275-6270",
number = "19",
volume = "40",
doi = "10.1016/j.ijhydene.2015.03.003",
url = "conv_547"
}

Perović, N. M., Aćimović, D. D., Tasić, G. S., Karić, S. D., Lausević, P. Z., Marčeta-Kaninski, M.,& Nikolić, V.. (2015). Efficient hydrogen production using ternary Ni-Cu-Mo ionic activator. in International Journal of Hydrogen Energy, 40(19), 6270-6275.
https://doi.org/10.1016/j.ijhydene.2015.03.003
conv_547

Perović NM, Aćimović DD, Tasić GS, Karić SD, Lausević PZ, Marčeta-Kaninski M, Nikolić V. Efficient hydrogen production using ternary Ni-Cu-Mo ionic activator. in International Journal of Hydrogen Energy. 2015;40(19):6270-6275.
doi:10.1016/j.ijhydene.2015.03.003
conv_547 .

Perović, Nana M., Aćimović, Danka D., Tasić, Gvozden S., Karić, Slavko D., Lausević, Petar Z., Marčeta-Kaninski, Milica, Nikolić, Vladimir, "Efficient hydrogen production using ternary Ni-Cu-Mo ionic activator" in International Journal of Hydrogen Energy, 40, no. 19 (2015):6270-6275,
https://doi.org/10.1016/j.ijhydene.2015.03.003 .,
conv_547 .

TY  - JOUR
AU  - Vasić-Anićijević, Dragana
AU  - Nikolić, Vladimir
AU  - Marčeta-Kaninski, Milica
AU  - Pasti, Igor A.
PY  - 2015
UR  - https://riofh.iofh.bg.ac.rs/handle/123456789/370
AB  - Tungsten carbide (WC) is in the focus of current research as a suitable electrocatalyst support. Typically, supported monometallic system are investigated, in spite the fact that practice in catalysis shows that multimetallic systems can have significantly better performance compared to monometallic counterparts. In this work, WC-supported Pd3Au overlayers were studied theoretically using periodic Density Functional Theory calculations and compared to bulk-like Pd3Au and pure Pd. Stability of studied surfaces and the electronic structures were analyzed. Chemisorption properties were probed using atomic H and CO molecule. Electrocatalytic activities of studied surfaces were estimated using hydrogen binding energy as catalytic activity descriptor for hydrogen electrode reactions. The connection between H binding energy and CO adsorption energy enabled us to establish the link between catalytic activity and CO tolerance of studied surfaces. It is considered that formation of bimetallic layers on WC opens a new perspective in designing new core-shell electrocatalysts with high performance and significantly reduced content of noble metals.
T2  - International Journal of Hydrogen Energy
T1  - Structure, chemisorption properties and electrocatalysis by Pd3Au overlayers on tungsten carbide - A DFT study
EP  - 6096
IS  - 18
SP  - 6085
VL  - 40
DO  - 10.1016/j.ijhydene.2015.03.083
UR  - conv_546
ER  - 

@article{
author = "Vasić-Anićijević, Dragana and Nikolić, Vladimir and Marčeta-Kaninski, Milica and Pasti, Igor A.",
year = "2015",
abstract = "Tungsten carbide (WC) is in the focus of current research as a suitable electrocatalyst support. Typically, supported monometallic system are investigated, in spite the fact that practice in catalysis shows that multimetallic systems can have significantly better performance compared to monometallic counterparts. In this work, WC-supported Pd3Au overlayers were studied theoretically using periodic Density Functional Theory calculations and compared to bulk-like Pd3Au and pure Pd. Stability of studied surfaces and the electronic structures were analyzed. Chemisorption properties were probed using atomic H and CO molecule. Electrocatalytic activities of studied surfaces were estimated using hydrogen binding energy as catalytic activity descriptor for hydrogen electrode reactions. The connection between H binding energy and CO adsorption energy enabled us to establish the link between catalytic activity and CO tolerance of studied surfaces. It is considered that formation of bimetallic layers on WC opens a new perspective in designing new core-shell electrocatalysts with high performance and significantly reduced content of noble metals.",
journal = "International Journal of Hydrogen Energy",
title = "Structure, chemisorption properties and electrocatalysis by Pd3Au overlayers on tungsten carbide - A DFT study",
pages = "6096-6085",
number = "18",
volume = "40",
doi = "10.1016/j.ijhydene.2015.03.083",
url = "conv_546"
}

Vasić-Anićijević, D., Nikolić, V., Marčeta-Kaninski, M.,& Pasti, I. A.. (2015). Structure, chemisorption properties and electrocatalysis by Pd3Au overlayers on tungsten carbide - A DFT study. in International Journal of Hydrogen Energy, 40(18), 6085-6096.
https://doi.org/10.1016/j.ijhydene.2015.03.083
conv_546

Vasić-Anićijević D, Nikolić V, Marčeta-Kaninski M, Pasti IA. Structure, chemisorption properties and electrocatalysis by Pd3Au overlayers on tungsten carbide - A DFT study. in International Journal of Hydrogen Energy. 2015;40(18):6085-6096.
doi:10.1016/j.ijhydene.2015.03.083
conv_546 .

Vasić-Anićijević, Dragana, Nikolić, Vladimir, Marčeta-Kaninski, Milica, Pasti, Igor A., "Structure, chemisorption properties and electrocatalysis by Pd3Au overlayers on tungsten carbide - A DFT study" in International Journal of Hydrogen Energy, 40, no. 18 (2015):6085-6096,
https://doi.org/10.1016/j.ijhydene.2015.03.083 .,
conv_546 .

TY  - JOUR
AU  - Nikolić, Vladimir
AU  - Perović, Ivana M.
AU  - Gavrilov, Nemanja M.
AU  - Pasti, Igor A.
AU  - Šaponjić, Aleksandra B.
AU  - Vulić, Predrag
AU  - Karić, Slavko D.
AU  - Babić, Biljana M.
AU  - Marčeta-Kaninski, Milica
PY  - 2014
UR  - https://riofh.iofh.bg.ac.rs/handle/123456789/331
AB  - Fuel cell application of tungsten carbide is revisited starting with four different tungsten carbide precursors used for high temperature synthesis. It was shown that the final products greatly depend on the nature of the precursor. Using tungsten peroxide/2-propanol derived precursor almost pure WC was obtained which was subjected to further electrochemical investigation. It was shown that it is necessary to decorate WC with Pt nanoparticles in order to obtain satisfactory fuel cell performance, but catalytic activity of Pt/WC anode catalyst is not expected to overcome the activity of Pt/C. It is argued that new synthetic routes for the preparation of WC should be directed towards obtaining highly dispersed WC, that is, WC with high external surface area available for Pt deposition, rather than high specific surface area WC with large contribution of micropores having no importance when it comes to the use of WC as a catalyst support. The true benefit of the use of WC as catalyst support is found in increased CO tolerance/CO oxidation activity of WC-supported Pt catalysts. Qualitative mechanistic view on increased CO oxidation activity of Pt/WC is offered.
T2  - International Journal of Hydrogen Energy
T1  - On the tungsten carbide synthesis for PEM fuel cell application - Problems, challenges and advantages
EP  - 11185
IS  - 21
SP  - 11175
VL  - 39
DO  - 10.1016/j.ijhydene.2014.05.078
UR  - conv_492
ER  - 

@article{
author = "Nikolić, Vladimir and Perović, Ivana M. and Gavrilov, Nemanja M. and Pasti, Igor A. and Šaponjić, Aleksandra B. and Vulić, Predrag and Karić, Slavko D. and Babić, Biljana M. and Marčeta-Kaninski, Milica",
year = "2014",
abstract = "Fuel cell application of tungsten carbide is revisited starting with four different tungsten carbide precursors used for high temperature synthesis. It was shown that the final products greatly depend on the nature of the precursor. Using tungsten peroxide/2-propanol derived precursor almost pure WC was obtained which was subjected to further electrochemical investigation. It was shown that it is necessary to decorate WC with Pt nanoparticles in order to obtain satisfactory fuel cell performance, but catalytic activity of Pt/WC anode catalyst is not expected to overcome the activity of Pt/C. It is argued that new synthetic routes for the preparation of WC should be directed towards obtaining highly dispersed WC, that is, WC with high external surface area available for Pt deposition, rather than high specific surface area WC with large contribution of micropores having no importance when it comes to the use of WC as a catalyst support. The true benefit of the use of WC as catalyst support is found in increased CO tolerance/CO oxidation activity of WC-supported Pt catalysts. Qualitative mechanistic view on increased CO oxidation activity of Pt/WC is offered.",
journal = "International Journal of Hydrogen Energy",
title = "On the tungsten carbide synthesis for PEM fuel cell application - Problems, challenges and advantages",
pages = "11185-11175",
number = "21",
volume = "39",
doi = "10.1016/j.ijhydene.2014.05.078",
url = "conv_492"
}

Nikolić, V., Perović, I. M., Gavrilov, N. M., Pasti, I. A., Šaponjić, A. B., Vulić, P., Karić, S. D., Babić, B. M.,& Marčeta-Kaninski, M.. (2014). On the tungsten carbide synthesis for PEM fuel cell application - Problems, challenges and advantages. in International Journal of Hydrogen Energy, 39(21), 11175-11185.
https://doi.org/10.1016/j.ijhydene.2014.05.078
conv_492

Nikolić V, Perović IM, Gavrilov NM, Pasti IA, Šaponjić AB, Vulić P, Karić SD, Babić BM, Marčeta-Kaninski M. On the tungsten carbide synthesis for PEM fuel cell application - Problems, challenges and advantages. in International Journal of Hydrogen Energy. 2014;39(21):11175-11185.
doi:10.1016/j.ijhydene.2014.05.078
conv_492 .

Nikolić, Vladimir, Perović, Ivana M., Gavrilov, Nemanja M., Pasti, Igor A., Šaponjić, Aleksandra B., Vulić, Predrag, Karić, Slavko D., Babić, Biljana M., Marčeta-Kaninski, Milica, "On the tungsten carbide synthesis for PEM fuel cell application - Problems, challenges and advantages" in International Journal of Hydrogen Energy, 39, no. 21 (2014):11175-11185,
https://doi.org/10.1016/j.ijhydene.2014.05.078 .,
conv_492 .

TY  - JOUR
AU  - Maslovara, Slađana
AU  - Miulović, Snežana M.
AU  - Marčeta-Kaninski, Milica
AU  - Tasić, Gvozden S.
AU  - Nikolić, Vladimir
PY  - 2013
UR  - https://riofh.iofh.bg.ac.rs/handle/123456789/258
AB  - Alkaline water electrolysis is one of the easiest methods for hydrogen production. Simplicity and usefulness are the two main features that characterize this method. The challenges for widespread use of water electrolysis are to reduce energy consumption, cost, durability and safety. In our investigation we obtain the results about energy efficiency system with the addition of ionic activators (i.a.) - Co(en)(3)Cl-3, Na2MoO4 and ZnCl2, in 6 M KOH solution. The requirements per mass unit of hydrogen produced are reduced up to 15% just using simplified process of the in situ activation with d-metals. The most important result of this study is that obtained deposit exhibit long-term stability at elevated temperatures and high current densities, like industrial conditions.
T2  - Applied Catalysis A-General
T1  - Energy consumption of the electrolytic hydrogen production using Zn-Co-Mo based activators-Part I
EP  - 219
SP  - 216
VL  - 451
DO  - 10.1016/j.apcata.2012.09.057
UR  - conv_438
ER  - 

@article{
author = "Maslovara, Slađana and Miulović, Snežana M. and Marčeta-Kaninski, Milica and Tasić, Gvozden S. and Nikolić, Vladimir",
year = "2013",
abstract = "Alkaline water electrolysis is one of the easiest methods for hydrogen production. Simplicity and usefulness are the two main features that characterize this method. The challenges for widespread use of water electrolysis are to reduce energy consumption, cost, durability and safety. In our investigation we obtain the results about energy efficiency system with the addition of ionic activators (i.a.) - Co(en)(3)Cl-3, Na2MoO4 and ZnCl2, in 6 M KOH solution. The requirements per mass unit of hydrogen produced are reduced up to 15% just using simplified process of the in situ activation with d-metals. The most important result of this study is that obtained deposit exhibit long-term stability at elevated temperatures and high current densities, like industrial conditions.",
journal = "Applied Catalysis A-General",
title = "Energy consumption of the electrolytic hydrogen production using Zn-Co-Mo based activators-Part I",
pages = "219-216",
volume = "451",
doi = "10.1016/j.apcata.2012.09.057",
url = "conv_438"
}

Maslovara, S., Miulović, S. M., Marčeta-Kaninski, M., Tasić, G. S.,& Nikolić, V.. (2013). Energy consumption of the electrolytic hydrogen production using Zn-Co-Mo based activators-Part I. in Applied Catalysis A-General, 451, 216-219.
https://doi.org/10.1016/j.apcata.2012.09.057
conv_438

Maslovara S, Miulović SM, Marčeta-Kaninski M, Tasić GS, Nikolić V. Energy consumption of the electrolytic hydrogen production using Zn-Co-Mo based activators-Part I. in Applied Catalysis A-General. 2013;451:216-219.
doi:10.1016/j.apcata.2012.09.057
conv_438 .

Maslovara, Slađana, Miulović, Snežana M., Marčeta-Kaninski, Milica, Tasić, Gvozden S., Nikolić, Vladimir, "Energy consumption of the electrolytic hydrogen production using Zn-Co-Mo based activators-Part I" in Applied Catalysis A-General, 451 (2013):216-219,
https://doi.org/10.1016/j.apcata.2012.09.057 .,
conv_438 .

TY  - JOUR
AU  - Miulović, Snežana M.
AU  - Maslovara, Slađana
AU  - Perović, Ivana M.
AU  - Nikolić, Vladimir
AU  - Marčeta-Kaninski, Milica
PY  - 2013
UR  - https://riofh.iofh.bg.ac.rs/handle/123456789/257
AB  - Nickel electrodes are widely used in industrial water electrolysis cells for electrochemical production of hydrogen. To avoid extensive deactivation problems and enhance the efficiency of the electrolyser cathode, in this work in situ activation is proposed using ionic activator (i.a.) based on combination of three d-metals: Zn, Co and Mo. Polarization curves, obtained at different temperatures (303-343 K), reveal that the addition of ZnCoMo based La. did not change reaction mechanism when compared to the HER mechanism on nickel cathode in standard electrolyte. The electrochemical impedance spectroscopy measurements were employed to further investigate the origin of obtained electrocatalytic effect on the HER. The morphology of obtained coatings was examined by scanning electron microscopy.
T2  - Applied Catalysis A-General
T1  - Electrocatalytic activity of ZnCoMo based ionic activators for alkaline hydrogen evolution-Part II
EP  - 226
SP  - 220
VL  - 451
DO  - 10.1016/j.apcata.2012.09.056
UR  - conv_439
ER  - 

@article{
author = "Miulović, Snežana M. and Maslovara, Slađana and Perović, Ivana M. and Nikolić, Vladimir and Marčeta-Kaninski, Milica",
year = "2013",
abstract = "Nickel electrodes are widely used in industrial water electrolysis cells for electrochemical production of hydrogen. To avoid extensive deactivation problems and enhance the efficiency of the electrolyser cathode, in this work in situ activation is proposed using ionic activator (i.a.) based on combination of three d-metals: Zn, Co and Mo. Polarization curves, obtained at different temperatures (303-343 K), reveal that the addition of ZnCoMo based La. did not change reaction mechanism when compared to the HER mechanism on nickel cathode in standard electrolyte. The electrochemical impedance spectroscopy measurements were employed to further investigate the origin of obtained electrocatalytic effect on the HER. The morphology of obtained coatings was examined by scanning electron microscopy.",
journal = "Applied Catalysis A-General",
title = "Electrocatalytic activity of ZnCoMo based ionic activators for alkaline hydrogen evolution-Part II",
pages = "226-220",
volume = "451",
doi = "10.1016/j.apcata.2012.09.056",
url = "conv_439"
}

Miulović, S. M., Maslovara, S., Perović, I. M., Nikolić, V.,& Marčeta-Kaninski, M.. (2013). Electrocatalytic activity of ZnCoMo based ionic activators for alkaline hydrogen evolution-Part II. in Applied Catalysis A-General, 451, 220-226.
https://doi.org/10.1016/j.apcata.2012.09.056
conv_439

Miulović SM, Maslovara S, Perović IM, Nikolić V, Marčeta-Kaninski M. Electrocatalytic activity of ZnCoMo based ionic activators for alkaline hydrogen evolution-Part II. in Applied Catalysis A-General. 2013;451:220-226.
doi:10.1016/j.apcata.2012.09.056
conv_439 .

Miulović, Snežana M., Maslovara, Slađana, Perović, Ivana M., Nikolić, Vladimir, Marčeta-Kaninski, Milica, "Electrocatalytic activity of ZnCoMo based ionic activators for alkaline hydrogen evolution-Part II" in Applied Catalysis A-General, 451 (2013):220-226,
https://doi.org/10.1016/j.apcata.2012.09.056 .,
conv_439 .