TY  - JOUR
AU  - Popović, Marko
AU  - Stevanović, Maja
AU  - Pantović Pavlović, Marijana
PY  - 2024-01
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/7595
AB  - Pertussis (whooping cough) has been nearly eradicated during the 20th century, first of all due to an organized and comprehensive vaccination campaign that lasted for decades. Generations of doctors educated in Serbia (and other countries) rarely had an opportunity to see the clinical picture of pertussis. However, during 2023, the number of registered cases of pertussis in Serbia has increased several times. This is why the health authorities were forced to declare danger of an epidemic. During 2023, in Belgrade, around 1000 cases were registered. During the two months of 2024, 400 cases were registered. Some of them have ended with lethal outcome. This paper reports for the first time the biosynthesis reaction and thermodynamic properties of biosynthesis (enthalpy, entropy and Gibbs energy) of Bordetella pertussis, the cause of whooping cough. Moreover, a mechanistic model of multiplication of B. pertussis was developed. The mechanistic model was related to the pathogenesis of pertussis.
PB  - Elsevier
T2  - Microbial Risk Analysis
T1  - Return of the forgotten nightmare: Bordetella pertussis uses a more negative Gibbs energy of metabolism to outcompete its host organism
VL  - 26
SP  - 100292
DO  - 10.1016/j.mran.2024.100292
ER  - 

@article{
author = "Popović, Marko and Stevanović, Maja and Pantović Pavlović, Marijana",
year = "2024-01",
abstract = "Pertussis (whooping cough) has been nearly eradicated during the 20th century, first of all due to an organized and comprehensive vaccination campaign that lasted for decades. Generations of doctors educated in Serbia (and other countries) rarely had an opportunity to see the clinical picture of pertussis. However, during 2023, the number of registered cases of pertussis in Serbia has increased several times. This is why the health authorities were forced to declare danger of an epidemic. During 2023, in Belgrade, around 1000 cases were registered. During the two months of 2024, 400 cases were registered. Some of them have ended with lethal outcome. This paper reports for the first time the biosynthesis reaction and thermodynamic properties of biosynthesis (enthalpy, entropy and Gibbs energy) of Bordetella pertussis, the cause of whooping cough. Moreover, a mechanistic model of multiplication of B. pertussis was developed. The mechanistic model was related to the pathogenesis of pertussis.",
publisher = "Elsevier",
journal = "Microbial Risk Analysis",
title = "Return of the forgotten nightmare: Bordetella pertussis uses a more negative Gibbs energy of metabolism to outcompete its host organism",
volume = "26",
pages = "100292",
doi = "10.1016/j.mran.2024.100292"
}

Popović, M., Stevanović, M.,& Pantović Pavlović, M.. (2024-01). Return of the forgotten nightmare: Bordetella pertussis uses a more negative Gibbs energy of metabolism to outcompete its host organism. in Microbial Risk Analysis
Elsevier., 26, 100292.
https://doi.org/10.1016/j.mran.2024.100292

Popović M, Stevanović M, Pantović Pavlović M. Return of the forgotten nightmare: Bordetella pertussis uses a more negative Gibbs energy of metabolism to outcompete its host organism. in Microbial Risk Analysis. 2024;26:100292.
doi:10.1016/j.mran.2024.100292 .

Popović, Marko, Stevanović, Maja, Pantović Pavlović, Marijana, "Return of the forgotten nightmare: Bordetella pertussis uses a more negative Gibbs energy of metabolism to outcompete its host organism" in Microbial Risk Analysis, 26 (2024-01):100292,
https://doi.org/10.1016/j.mran.2024.100292 . .

TY  - CONF
AU  - Košević, Milica
AU  - Nikolić, Nebojša
AU  - Lović, Jelena
PY  - 2024
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/7652
AB  - Racionalno projektovanje materijala na bazi plemenitih metala je od velikog interesa za njihovu primenu u oblasti elektrokatalize. U ovom radu prikazana je galvanostatska priprema Pd iz rastvora bez surfaktanata. Analiza skenirajuće elektronske mikroskopije pokazala je nanosfere Pd veličine do 300 nm. Uporednim ispitivanjem oksidacije metanola i etanola utvrđena je veća aktivnost katalizatora u rastvoru LiOH u odnosu na rastvor NaOH usled formiranja klastera OHad ‒ katjona. Naime, nekovalentna interakcija i formiranje OHad ‒ katjonskih klastera određuju interakciju alkoholne OH grupe sa OH grupom na površini Pd, i posledično određuju aktivnost Pd u ispitivanim reakcijama. Može se zaključiti da izbor katjona alkalnih metala reguliše elektrokatalitičku aktivnost i da se može smatrati jednim od bitnih parametara u elektrokatalizi.
AB  - Rationally designing of noble metal materials are of great interest for supporting their applications in the field of electrocatalysis. In this contribution, we demonstrated the galvanostatic preparation of Pd from surfactant free solution. Scanning electron microscopy analysis revealed Pd nanospheres of up to 300 nm. Comparative study of methanol and ethanol electrochemical oxidation reveals higher catalyst activity in LiOH solution in regard to NaOH solution due to the formation of OHad ‒ cation clusters. Namely non-covalent interaction and formation of OHad ‒ cation clusters govern the interaction of the alcohol OH group with the OH group on the Pd surface, and in turn determined its electrooxidation activity on Pd. It was pointed out that the choice of alkali metal cations regulate the electrocatalytic activity and can be considered as one of the tuning parameter in electrocatalysis.
PB  - Srpsko hemijsko društvo
C3  - 60. Savetovanje Srpskog hemijskog društva - Kratki izvodi radova, Niš 8. i 9. jun 2024. godine
T1  - Aktivnost elektrohemijski taloženih nanosfera Pd u reakcijama oksidacije metanola i etanola u alkalnim rastvorima
T1  - Activity of electrodeposited Pd nanospheres in methanol and ethanol oxidation in alkaline solutions
SP  - 56
EP  - 56
ER  - 

@conference{
author = "Košević, Milica and Nikolić, Nebojša and Lović, Jelena",
year = "2024",
abstract = "Racionalno projektovanje materijala na bazi plemenitih metala je od velikog interesa za njihovu primenu u oblasti elektrokatalize. U ovom radu prikazana je galvanostatska priprema Pd iz rastvora bez surfaktanata. Analiza skenirajuće elektronske mikroskopije pokazala je nanosfere Pd veličine do 300 nm. Uporednim ispitivanjem oksidacije metanola i etanola utvrđena je veća aktivnost katalizatora u rastvoru LiOH u odnosu na rastvor NaOH usled formiranja klastera OHad ‒ katjona. Naime, nekovalentna interakcija i formiranje OHad ‒ katjonskih klastera određuju interakciju alkoholne OH grupe sa OH grupom na površini Pd, i posledično određuju aktivnost Pd u ispitivanim reakcijama. Može se zaključiti da izbor katjona alkalnih metala reguliše elektrokatalitičku aktivnost i da se može smatrati jednim od bitnih parametara u elektrokatalizi., Rationally designing of noble metal materials are of great interest for supporting their applications in the field of electrocatalysis. In this contribution, we demonstrated the galvanostatic preparation of Pd from surfactant free solution. Scanning electron microscopy analysis revealed Pd nanospheres of up to 300 nm. Comparative study of methanol and ethanol electrochemical oxidation reveals higher catalyst activity in LiOH solution in regard to NaOH solution due to the formation of OHad ‒ cation clusters. Namely non-covalent interaction and formation of OHad ‒ cation clusters govern the interaction of the alcohol OH group with the OH group on the Pd surface, and in turn determined its electrooxidation activity on Pd. It was pointed out that the choice of alkali metal cations regulate the electrocatalytic activity and can be considered as one of the tuning parameter in electrocatalysis.",
publisher = "Srpsko hemijsko društvo",
journal = "60. Savetovanje Srpskog hemijskog društva - Kratki izvodi radova, Niš 8. i 9. jun 2024. godine",
title = "Aktivnost elektrohemijski taloženih nanosfera Pd u reakcijama oksidacije metanola i etanola u alkalnim rastvorima, Activity of electrodeposited Pd nanospheres in methanol and ethanol oxidation in alkaline solutions",
pages = "56-56"
}

Košević, M., Nikolić, N.,& Lović, J.. (2024). Aktivnost elektrohemijski taloženih nanosfera Pd u reakcijama oksidacije metanola i etanola u alkalnim rastvorima. in 60. Savetovanje Srpskog hemijskog društva - Kratki izvodi radova, Niš 8. i 9. jun 2024. godine
Srpsko hemijsko društvo., 56-56.

Košević M, Nikolić N, Lović J. Aktivnost elektrohemijski taloženih nanosfera Pd u reakcijama oksidacije metanola i etanola u alkalnim rastvorima. in 60. Savetovanje Srpskog hemijskog društva - Kratki izvodi radova, Niš 8. i 9. jun 2024. godine. 2024;:56-56..

Košević, Milica, Nikolić, Nebojša, Lović, Jelena, "Aktivnost elektrohemijski taloženih nanosfera Pd u reakcijama oksidacije metanola i etanola u alkalnim rastvorima" in 60. Savetovanje Srpskog hemijskog društva - Kratki izvodi radova, Niš 8. i 9. jun 2024. godine (2024):56-56.

TY  - CONF
AU  - Marković, Olivera
AU  - Mrđinac, Jelena Ž.
AU  - Pepić, Sara
AU  - Verbić, Tatjana
PY  - 2024
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/7656
AB  - The solubility profile of a drug typically consists of two independent curves that intersect 
at a specific point called pHmax. At pHmax, both salt and base coexist as solid phases. While 
two solids coexist, pH and solubility in the heterogeneous system remain constant 
(according to the Gibbs Phase Rule). Recent studies, however, have shown that pH and 
solubility might change during the salt-to-free-base transformation. This pH range, 
containing two solids, is termed the pHmax – pHmin range. pHmax refers to the pH value at 
the maximum solubility of a eutectic mixture, whereas pHmin represents the pH value at the 
minimum solubility of the eutectic mixture. The objective of this study was to investigate 
the influence of suspension concentration (the ratio of drug mass to suspension volume) on 
the pHmax – pHmin range during solubility determination using the pH-Ramp shake-flask
method. Nortriptyline hydrochloride (Nor, monoprotic base) and atorvastatin calcium (At, 
monoprotic acid) were employed as model compounds. Results indicate that the pHmax –
pHmin range increases as suspension concentration rises (for 20.10 mg NorHCl/mL: 
pHmax=3.55, ΔpH=0; for 59.82 mg NorHCl/mL: pHmax – pHmin= 3.56 – 4.52, ΔpH=0.96). 
Understanding the details of the pHmax – pHmin range could significantly impact product 
formulation optimization in drug research.
AB  - Cilj ovog rada bio je ispitivanje uticaja koncentracije suspenzije na širinu pHmax – pHmin
opsega tokom određivanja rastvorljivosti pH-Ramp shake-flask metodom. Kao model 
jedinjenja izabrani su nortriptilin-hidrohlorid i atorvastatin-kalcijum. Rezultati su pokazali 
da sa porastom koncentracije suspenzije dolazi do širenja opsega pHmax – pHmin, a ovakva 
proučavanja mogu značajno doprineti optimizaciji formulacije u procesu dizajna i razvoja 
lekova.
PB  - Serbian Chemical Society
C3  - 60th Meeting of the Serbian Chemical Society - Book of Abstracts, Niš, Serbia, June 8-9, 2024
T1  - The influence of suspension concentration on the pHmax – pHmin range during the solubility determination
T1  - Ispitivanje uticaja koncentracije suspenzije na širinu pHmax – pHmin opsega tokom određivanja rastvorljivosti
SP  - 47
EP  - 47
ER  - 

@conference{
author = "Marković, Olivera and Mrđinac, Jelena Ž. and Pepić, Sara and Verbić, Tatjana",
year = "2024",
abstract = "The solubility profile of a drug typically consists of two independent curves that intersect 
at a specific point called pHmax. At pHmax, both salt and base coexist as solid phases. While 
two solids coexist, pH and solubility in the heterogeneous system remain constant 
(according to the Gibbs Phase Rule). Recent studies, however, have shown that pH and 
solubility might change during the salt-to-free-base transformation. This pH range, 
containing two solids, is termed the pHmax – pHmin range. pHmax refers to the pH value at 
the maximum solubility of a eutectic mixture, whereas pHmin represents the pH value at the 
minimum solubility of the eutectic mixture. The objective of this study was to investigate 
the influence of suspension concentration (the ratio of drug mass to suspension volume) on 
the pHmax – pHmin range during solubility determination using the pH-Ramp shake-flask
method. Nortriptyline hydrochloride (Nor, monoprotic base) and atorvastatin calcium (At, 
monoprotic acid) were employed as model compounds. Results indicate that the pHmax –
pHmin range increases as suspension concentration rises (for 20.10 mg NorHCl/mL: 
pHmax=3.55, ΔpH=0; for 59.82 mg NorHCl/mL: pHmax – pHmin= 3.56 – 4.52, ΔpH=0.96). 
Understanding the details of the pHmax – pHmin range could significantly impact product 
formulation optimization in drug research., Cilj ovog rada bio je ispitivanje uticaja koncentracije suspenzije na širinu pHmax – pHmin
opsega tokom određivanja rastvorljivosti pH-Ramp shake-flask metodom. Kao model 
jedinjenja izabrani su nortriptilin-hidrohlorid i atorvastatin-kalcijum. Rezultati su pokazali 
da sa porastom koncentracije suspenzije dolazi do širenja opsega pHmax – pHmin, a ovakva 
proučavanja mogu značajno doprineti optimizaciji formulacije u procesu dizajna i razvoja 
lekova.",
publisher = "Serbian Chemical Society",
journal = "60th Meeting of the Serbian Chemical Society - Book of Abstracts, Niš, Serbia, June 8-9, 2024",
title = "The influence of suspension concentration on the pHmax – pHmin range during the solubility determination, Ispitivanje uticaja koncentracije suspenzije na širinu pHmax – pHmin opsega tokom određivanja rastvorljivosti",
pages = "47-47"
}

Marković, O., Mrđinac, J. Ž., Pepić, S.,& Verbić, T.. (2024). The influence of suspension concentration on the pHmax – pHmin range during the solubility determination. in 60th Meeting of the Serbian Chemical Society - Book of Abstracts, Niš, Serbia, June 8-9, 2024
Serbian Chemical Society., 47-47.

Marković O, Mrđinac JŽ, Pepić S, Verbić T. The influence of suspension concentration on the pHmax – pHmin range during the solubility determination. in 60th Meeting of the Serbian Chemical Society - Book of Abstracts, Niš, Serbia, June 8-9, 2024. 2024;:47-47..

Marković, Olivera, Mrđinac, Jelena Ž., Pepić, Sara, Verbić, Tatjana, "The influence of suspension concentration on the pHmax – pHmin range during the solubility determination" in 60th Meeting of the Serbian Chemical Society - Book of Abstracts, Niš, Serbia, June 8-9, 2024 (2024):47-47.

TY  - CONF
AU  - Božić, Katarina
AU  - Pavlović, Miroslav
AU  - Kojić, Vesna V.
AU  - Veljović, Đorđe
AU  - Pantović Pavlović, Marijana
PY  - 2024
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/7655
AB  - INTRODUCTION: Hydroxyapatite, the main inorganic component of human bone, is a widely used bioceramic for bone implant coatings due to its chemical and structural similarity with bone minerals and approved biocompatibility. Nowadays, the surface properties of implants are also modified by the addition of different biopolymers. Features such as biocompatibility, tuned biodegradability, and non-cytotoxicity make these materials excellent candidates for these applications. Zein is one of the natural polymers that has gained great interest for biomedical applications due to its natural renewable resource, biodegradability, biocompatibility and potential antibacterial activity.
EXPERIMENTAL: In this study, zein/titanium dioxide (zein/TiO2), hydroxyapatite/zein/titanium dioxide (HAp/zein/TiO2) and strontium-doped hydroxyapatite/zein/titanium dioxide (Sr-HAp/zein/TiO2) coatings were obtained on a titanium substrate by in situ anodization/anaphoretic deposition method at a constant voltage of 60 V and deposition time of 1 min. For the fabrication of HAp/zein/TiO2 and Sr-HAp/zein/TiO2 composite coatings, HAp and Sr-HAp nano-sized powders obtained by a modified chemical precipitation method were used. The microstructure and morphology of all coatings were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and scanning electron microscopy (SEM). Adhesion strength was measured according to the ASTM D3359-02 standard. Morphology and cell adhesion were analyzed by SEM.
RESULTS AND DISCUSSION: The advantage of this methodological approach compared to cataphoretic deposition is reflected in the simultaneous performance of several processes. The first is the anodization of the substrate surface, whereby a passive oxide layer (TiO2) is formed on the surface, which changes the structure and increases the surface roughness in a controlled manner. Another parallel process is the deposition of the HAp based coatings on the substrate. This way of coating formation shows better results than cataphoretic deposition in terms of better coating adhesion to the substrate. Adhesion strength was significantly improved compared to coatings obtained by cataphoretic processes, without the need for subsequent treatment. Cytotoxicity tests showed that there was no significant decrease in the survival of healthy human lung fibroblasts (MRC-5) cells exposed to the obtained coatings.
CONCLUSIONS: Altogether, zein/TiO2, HAp/zein/TiO2 and Sr-HAp/zein/TiO2 could be promising non-toxic biomaterials for orthopedic and dental applications.
PB  - Savez hemijskih inženjera Srbije
C3  - Chemical Industry - Supplementary Issue
T1  - Anodization/anaphoretic deposition of composite zein/hydroxyapatite coatings on titanium substrate
VL  - 78
IS  - 1S
SP  - 42
EP  - 42
ER  - 

@conference{
author = "Božić, Katarina and Pavlović, Miroslav and Kojić, Vesna V. and Veljović, Đorđe and Pantović Pavlović, Marijana",
year = "2024",
abstract = "INTRODUCTION: Hydroxyapatite, the main inorganic component of human bone, is a widely used bioceramic for bone implant coatings due to its chemical and structural similarity with bone minerals and approved biocompatibility. Nowadays, the surface properties of implants are also modified by the addition of different biopolymers. Features such as biocompatibility, tuned biodegradability, and non-cytotoxicity make these materials excellent candidates for these applications. Zein is one of the natural polymers that has gained great interest for biomedical applications due to its natural renewable resource, biodegradability, biocompatibility and potential antibacterial activity.
EXPERIMENTAL: In this study, zein/titanium dioxide (zein/TiO2), hydroxyapatite/zein/titanium dioxide (HAp/zein/TiO2) and strontium-doped hydroxyapatite/zein/titanium dioxide (Sr-HAp/zein/TiO2) coatings were obtained on a titanium substrate by in situ anodization/anaphoretic deposition method at a constant voltage of 60 V and deposition time of 1 min. For the fabrication of HAp/zein/TiO2 and Sr-HAp/zein/TiO2 composite coatings, HAp and Sr-HAp nano-sized powders obtained by a modified chemical precipitation method were used. The microstructure and morphology of all coatings were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and scanning electron microscopy (SEM). Adhesion strength was measured according to the ASTM D3359-02 standard. Morphology and cell adhesion were analyzed by SEM.
RESULTS AND DISCUSSION: The advantage of this methodological approach compared to cataphoretic deposition is reflected in the simultaneous performance of several processes. The first is the anodization of the substrate surface, whereby a passive oxide layer (TiO2) is formed on the surface, which changes the structure and increases the surface roughness in a controlled manner. Another parallel process is the deposition of the HAp based coatings on the substrate. This way of coating formation shows better results than cataphoretic deposition in terms of better coating adhesion to the substrate. Adhesion strength was significantly improved compared to coatings obtained by cataphoretic processes, without the need for subsequent treatment. Cytotoxicity tests showed that there was no significant decrease in the survival of healthy human lung fibroblasts (MRC-5) cells exposed to the obtained coatings.
CONCLUSIONS: Altogether, zein/TiO2, HAp/zein/TiO2 and Sr-HAp/zein/TiO2 could be promising non-toxic biomaterials for orthopedic and dental applications.",
publisher = "Savez hemijskih inženjera Srbije",
journal = "Chemical Industry - Supplementary Issue",
title = "Anodization/anaphoretic deposition of composite zein/hydroxyapatite coatings on titanium substrate",
volume = "78",
number = "1S",
pages = "42-42"
}

Božić, K., Pavlović, M., Kojić, V. V., Veljović, Đ.,& Pantović Pavlović, M.. (2024). Anodization/anaphoretic deposition of composite zein/hydroxyapatite coatings on titanium substrate. in Chemical Industry - Supplementary Issue
Savez hemijskih inženjera Srbije., 78(1S), 42-42.

Božić K, Pavlović M, Kojić VV, Veljović Đ, Pantović Pavlović M. Anodization/anaphoretic deposition of composite zein/hydroxyapatite coatings on titanium substrate. in Chemical Industry - Supplementary Issue. 2024;78(1S):42-42..

Božić, Katarina, Pavlović, Miroslav, Kojić, Vesna V., Veljović, Đorđe, Pantović Pavlović, Marijana, "Anodization/anaphoretic deposition of composite zein/hydroxyapatite coatings on titanium substrate" in Chemical Industry - Supplementary Issue, 78, no. 1S (2024):42-42.

TY  - JOUR
AU  - Marinović, Sanja
AU  - Mudrinić, Tihana
AU  - Ajduković, Marija
AU  - Jović-Jovičić, Nataša
AU  - Nikolova, Dimitrinka
AU  - Banković, Predrag
AU  - Novaković, Tatjana
PY  - 2024
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/7654
AB  - Cobalt-doped alumina catalyst calcined at 500 ºC (CoA-500) was investigated in the degradation of anionic textile dye Orange G in the presence of Oxone®. Different reaction parameters were altered in order to study their influence on Orange G degradation. The increase of the Oxone® dosage, mass of the catalyst and temperature was beneficial for the dye degradation rate. The best catalytic performance was obtained in the range of the initial solution pH = 6–8. Simultaneous degradation of both Orange G and cationic textile dye Basic blue 41, was also tested. The degradation of the Basic blue 41 did not occur while Orange G was present in the system. CoA-500 was found to be efficient catalyst in the Oxone® induced catalytic degradation of textile dyes.
PB  - International Institute for the Science of Sintering
T2  - Science of sintering
T1  - Oxone® induced textile dyes degradation using cobalt-doped alumina catalyst
VL  - OnLine-First
DO  - 10.2298/SOS230911066M
ER  - 

@article{
author = "Marinović, Sanja and Mudrinić, Tihana and Ajduković, Marija and Jović-Jovičić, Nataša and Nikolova, Dimitrinka and Banković, Predrag and Novaković, Tatjana",
year = "2024",
abstract = "Cobalt-doped alumina catalyst calcined at 500 ºC (CoA-500) was investigated in the degradation of anionic textile dye Orange G in the presence of Oxone®. Different reaction parameters were altered in order to study their influence on Orange G degradation. The increase of the Oxone® dosage, mass of the catalyst and temperature was beneficial for the dye degradation rate. The best catalytic performance was obtained in the range of the initial solution pH = 6–8. Simultaneous degradation of both Orange G and cationic textile dye Basic blue 41, was also tested. The degradation of the Basic blue 41 did not occur while Orange G was present in the system. CoA-500 was found to be efficient catalyst in the Oxone® induced catalytic degradation of textile dyes.",
publisher = "International Institute for the Science of Sintering",
journal = "Science of sintering",
title = "Oxone® induced textile dyes degradation using cobalt-doped alumina catalyst",
volume = "OnLine-First",
doi = "10.2298/SOS230911066M"
}

Marinović, S., Mudrinić, T., Ajduković, M., Jović-Jovičić, N., Nikolova, D., Banković, P.,& Novaković, T.. (2024). Oxone® induced textile dyes degradation using cobalt-doped alumina catalyst. in Science of sintering
International Institute for the Science of Sintering., OnLine-First.
https://doi.org/10.2298/SOS230911066M

Marinović S, Mudrinić T, Ajduković M, Jović-Jovičić N, Nikolova D, Banković P, Novaković T. Oxone® induced textile dyes degradation using cobalt-doped alumina catalyst. in Science of sintering. 2024;OnLine-First.
doi:10.2298/SOS230911066M .

Marinović, Sanja, Mudrinić, Tihana, Ajduković, Marija, Jović-Jovičić, Nataša, Nikolova, Dimitrinka, Banković, Predrag, Novaković, Tatjana, "Oxone® induced textile dyes degradation using cobalt-doped alumina catalyst" in Science of sintering, OnLine-First (2024),
https://doi.org/10.2298/SOS230911066M . .

TY  - CONF
AU  - Pantić, Olga
AU  - Panić, Vesna
AU  - Marković, Maja
AU  - Spasojević Savković, Milica
AU  - Spasojević, Pavle
AU  - Savić, Sanja
AU  - Kalagasidis Krušić, Melina
PY  - 2024
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/7653
AB  - Ekološki prihvatljive nezasićene poliestarske smole sa svojstvima sličnim 
 komercijalnim smolama dobijenim iz petrohemijskih sirovina u fokusu su novijih istraživanja zasnovanih na principima održivog razvoja. Jedan od glavnih izazova pri umreževanju je pravilan izbor inicijator/aktivator sistema za reakciju umrežavanja. U ovom radu je ispitan uticaj odnosa metil etil keton peroksida kao inicijatora i kobalt oktoata kao aktivatora na svojstva sintetisane nezasićene poliestarske smole na bazi itakonata. Utvrđen je optimalan sastav sistema inicijator/aktivator od 1,5:1,0 mas.%, pri kom je umrežena smola najveće zatezne 
čvrstoće i stepena umreženja. Pokazano je da povećanjem udela inicijatora u datom sistemu inicijator/aktivator od samo 4 puta dolazi do desetostrukog povećanja vrednosti zatezne čvrstoće.
AB  - Novel research guided by sustainable development principles aims to generate eco-friendly unsaturated polyester resins with comparable properties to commercial petroleum-based resins. One of the main challenges encountered is the proper selection of the 
initiator/activator system for the crosslinking reaction. In this research, the influence of the ratio of methyl ethyl ketone peroxide as an initiator and cobalt octoate as an activator on the properties of the synthesized itaconate based unsaturated polyester resin was studied. The optimal composition of the initiator/activator system was found to be 1.5:1.0 wt.%, at which the cured resin showed the highest tensile strength and degree of crosslinking. It was further shown that a fourfold increase of initiator in a given initiator/activator system resulted in increased value of tensile strength by an order of magnitude.
PB  - Srpsko hemijsko društvo
PB  - Serbian Chemical Society
C3  - 60. Savetovanje Srpskog hemijskog društva - Kratki izvodi radova, Niš 8. i 9. jun 2024. godine
T1  - Optimizacija procesa umrežavanja ekološki prihvatljive nezasićene  poliestarske smole
T1  - The curing process optimization of an eco-friendly unsaturated  polyester resin
SP  - 127
EP  - 1127
ER  - 

@conference{
author = "Pantić, Olga and Panić, Vesna and Marković, Maja and Spasojević Savković, Milica and Spasojević, Pavle and Savić, Sanja and Kalagasidis Krušić, Melina",
year = "2024",
abstract = "Ekološki prihvatljive nezasićene poliestarske smole sa svojstvima sličnim 
 komercijalnim smolama dobijenim iz petrohemijskih sirovina u fokusu su novijih istraživanja zasnovanih na principima održivog razvoja. Jedan od glavnih izazova pri umreževanju je pravilan izbor inicijator/aktivator sistema za reakciju umrežavanja. U ovom radu je ispitan uticaj odnosa metil etil keton peroksida kao inicijatora i kobalt oktoata kao aktivatora na svojstva sintetisane nezasićene poliestarske smole na bazi itakonata. Utvrđen je optimalan sastav sistema inicijator/aktivator od 1,5:1,0 mas.%, pri kom je umrežena smola najveće zatezne 
čvrstoće i stepena umreženja. Pokazano je da povećanjem udela inicijatora u datom sistemu inicijator/aktivator od samo 4 puta dolazi do desetostrukog povećanja vrednosti zatezne čvrstoće., Novel research guided by sustainable development principles aims to generate eco-friendly unsaturated polyester resins with comparable properties to commercial petroleum-based resins. One of the main challenges encountered is the proper selection of the 
initiator/activator system for the crosslinking reaction. In this research, the influence of the ratio of methyl ethyl ketone peroxide as an initiator and cobalt octoate as an activator on the properties of the synthesized itaconate based unsaturated polyester resin was studied. The optimal composition of the initiator/activator system was found to be 1.5:1.0 wt.%, at which the cured resin showed the highest tensile strength and degree of crosslinking. It was further shown that a fourfold increase of initiator in a given initiator/activator system resulted in increased value of tensile strength by an order of magnitude.",
publisher = "Srpsko hemijsko društvo, Serbian Chemical Society",
journal = "60. Savetovanje Srpskog hemijskog društva - Kratki izvodi radova, Niš 8. i 9. jun 2024. godine",
title = "Optimizacija procesa umrežavanja ekološki prihvatljive nezasićene  poliestarske smole, The curing process optimization of an eco-friendly unsaturated  polyester resin",
pages = "127-1127"
}

Pantić, O., Panić, V., Marković, M., Spasojević Savković, M., Spasojević, P., Savić, S.,& Kalagasidis Krušić, M.. (2024). Optimizacija procesa umrežavanja ekološki prihvatljive nezasićene  poliestarske smole. in 60. Savetovanje Srpskog hemijskog društva - Kratki izvodi radova, Niš 8. i 9. jun 2024. godine
Srpsko hemijsko društvo., 127-1127.

Pantić O, Panić V, Marković M, Spasojević Savković M, Spasojević P, Savić S, Kalagasidis Krušić M. Optimizacija procesa umrežavanja ekološki prihvatljive nezasićene  poliestarske smole. in 60. Savetovanje Srpskog hemijskog društva - Kratki izvodi radova, Niš 8. i 9. jun 2024. godine. 2024;:127-1127..

Pantić, Olga, Panić, Vesna, Marković, Maja, Spasojević Savković, Milica, Spasojević, Pavle, Savić, Sanja, Kalagasidis Krušić, Melina, "Optimizacija procesa umrežavanja ekološki prihvatljive nezasićene  poliestarske smole" in 60. Savetovanje Srpskog hemijskog društva - Kratki izvodi radova, Niš 8. i 9. jun 2024. godine (2024):127-1127.

TY  - CONF
AU  - Petrović, Nataša M.
AU  - Cvetković, Vesna. S
AU  - Jović, Vladimir D
AU  - Barudžija, Tanja
AU  - Jovićević, Jovan J.
PY  - 2024
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/7651
AB  - Transition metal oxides (TMOs) have gathered increasing attention in material science due to their good electrical,
mechanical, optical properties and great chemical and thermal stability. Among them, ruthenium oxide (RuO2), with
its excellent catalytic performances has been the subject of numerous studies. It serves as a crucial material for
electrodes in (electro)catalysis, energy storage systems, and semiconductor devices. RuO2-based catalysts have
shown good potential in many important reactions such as the low-temperature dehydrogenation of small
molecules (NH3, HCl, methanol), and have been utilized in industrial electrolysis for chlorine-alkali production [1,2].
There are numerous techniques to synthesize RuO2 [1]. In response to the challenges associated with RuO2
synthesis, and to customize the particle size and shape of RuO2, an electrochemical deposition from a new class of
non-aqueous electrolytes, namely the deep eutectic solvents (DESs), can be a good alternative. So far, there have
been recorded some attempts to electrochemically deposit ruthenium/ruthenium oxides from DES [3,4].
This study focuses on the electrochemical deposition of ruthenium oxide onto palladium working electrode from
choline chloride (ChCl): urea (1:2 ratio) DES at 80 °C with 0.01M Ru(III) ions concentration. RuCl3 was added as a
source of Ru ions in the working electrolyte. To determine the potential range available for Ru electrodeposition in
DES, cyclic voltammetry (CV) on Pd working electrode in the electrolyte containing ChCl and urea was recorded.
The potential window of electrochemical stability was between -1.2 and +0.3V vs. Pt. The electrochemical behaviour
of Ru(III) in choline chloride-urea has been investigated at palladium using cyclic voltammetry (CV) and square wave
voltammetry (SWV). The CV results showed only cathodic peaks without corresponding anodic counterparts, and
SWV was used for further investigation in order to gain a better understanding of the Ru(III) electroreduction
process. The electrochemical impedance spectroscopy (EIS) results indicate diffusion-controlled RuO2 deposition.
Relatively small deposition overpotential (-1.0 V) applied in the electrodeposition experiments, resulted in
ruthenium oxide being electrodeposited. The morphology of the obtained deposits was characterized using
scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS). X-ray diffraction (XRD) analysis of
the produced particles provided conformation that the RuO2 was formed onto a palladium working substrate.
PB  - Serbian Chemical Society
C3  - 9th Regional Symposium on Electrochemistry - South-East Europe, Book of Abstract, 3 to 7 June, 2024, Novi Sad, Serbia
T1  - Electrochemical deposition of ruthenium oxide from deep eutectic solvent
SP  - 98
EP  - 98
DO  - 10.5281/zenodo.11194247
ER  - 

@conference{
author = "Petrović, Nataša M. and Cvetković, Vesna. S and Jović, Vladimir D and Barudžija, Tanja and Jovićević, Jovan J.",
year = "2024",
abstract = "Transition metal oxides (TMOs) have gathered increasing attention in material science due to their good electrical,
mechanical, optical properties and great chemical and thermal stability. Among them, ruthenium oxide (RuO2), with
its excellent catalytic performances has been the subject of numerous studies. It serves as a crucial material for
electrodes in (electro)catalysis, energy storage systems, and semiconductor devices. RuO2-based catalysts have
shown good potential in many important reactions such as the low-temperature dehydrogenation of small
molecules (NH3, HCl, methanol), and have been utilized in industrial electrolysis for chlorine-alkali production [1,2].
There are numerous techniques to synthesize RuO2 [1]. In response to the challenges associated with RuO2
synthesis, and to customize the particle size and shape of RuO2, an electrochemical deposition from a new class of
non-aqueous electrolytes, namely the deep eutectic solvents (DESs), can be a good alternative. So far, there have
been recorded some attempts to electrochemically deposit ruthenium/ruthenium oxides from DES [3,4].
This study focuses on the electrochemical deposition of ruthenium oxide onto palladium working electrode from
choline chloride (ChCl): urea (1:2 ratio) DES at 80 °C with 0.01M Ru(III) ions concentration. RuCl3 was added as a
source of Ru ions in the working electrolyte. To determine the potential range available for Ru electrodeposition in
DES, cyclic voltammetry (CV) on Pd working electrode in the electrolyte containing ChCl and urea was recorded.
The potential window of electrochemical stability was between -1.2 and +0.3V vs. Pt. The electrochemical behaviour
of Ru(III) in choline chloride-urea has been investigated at palladium using cyclic voltammetry (CV) and square wave
voltammetry (SWV). The CV results showed only cathodic peaks without corresponding anodic counterparts, and
SWV was used for further investigation in order to gain a better understanding of the Ru(III) electroreduction
process. The electrochemical impedance spectroscopy (EIS) results indicate diffusion-controlled RuO2 deposition.
Relatively small deposition overpotential (-1.0 V) applied in the electrodeposition experiments, resulted in
ruthenium oxide being electrodeposited. The morphology of the obtained deposits was characterized using
scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS). X-ray diffraction (XRD) analysis of
the produced particles provided conformation that the RuO2 was formed onto a palladium working substrate.",
publisher = "Serbian Chemical Society",
journal = "9th Regional Symposium on Electrochemistry - South-East Europe, Book of Abstract, 3 to 7 June, 2024, Novi Sad, Serbia",
title = "Electrochemical deposition of ruthenium oxide from deep eutectic solvent",
pages = "98-98",
doi = "10.5281/zenodo.11194247"
}

Petrović, N. M., Cvetković, Vesna. S., Jović, V. D., Barudžija, T.,& Jovićević, J. J.. (2024). Electrochemical deposition of ruthenium oxide from deep eutectic solvent. in 9th Regional Symposium on Electrochemistry - South-East Europe, Book of Abstract, 3 to 7 June, 2024, Novi Sad, Serbia
Serbian Chemical Society., 98-98.
https://doi.org/10.5281/zenodo.11194247

Petrović NM, Cvetković VS, Jović VD, Barudžija T, Jovićević JJ. Electrochemical deposition of ruthenium oxide from deep eutectic solvent. in 9th Regional Symposium on Electrochemistry - South-East Europe, Book of Abstract, 3 to 7 June, 2024, Novi Sad, Serbia. 2024;:98-98.
doi:10.5281/zenodo.11194247 .

Petrović, Nataša M., Cvetković, Vesna. S, Jović, Vladimir D, Barudžija, Tanja, Jovićević, Jovan J., "Electrochemical deposition of ruthenium oxide from deep eutectic solvent" in 9th Regional Symposium on Electrochemistry - South-East Europe, Book of Abstract, 3 to 7 June, 2024, Novi Sad, Serbia (2024):98-98,
https://doi.org/10.5281/zenodo.11194247 . .

TY  - CONF
AU  - Petrović, Nataša M.
AU  - Cvetković, Vesna. S
AU  - Prasakti, Laras
AU  - Feldhaus, Dominic
AU  - Friedrich, Bernd
AU  - Jovićević, Jovan J.
AU  - Petrović, Nataša
PY  - 2024
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/7650
AB  - In the progressive energy transition process, rare earth elements (REE) became key components in crucial products
that play a central role in the development of renewable energy and low-carbon technologies. With China currently
producing more than 90 % of the world's REE output, many of the world's economies are facing REE supply risk [1].
To address this problem, many countries need to look for alternative resources of rare earths, e.g. recycling of these
elements from REE-containing end-of-life products. A new route for recovery of REE from NdFeB magnet scrap,
using a combination of pyrometallurgical treatment of spent NdFeB magnets, and a subsequent molten salt
electrolysis process, has been investigated in the authors’ laboratory [2]. The magnet recycling derived oxides
(MRDO), were produced from spent NdFeB magnets by oxidation in air and subsequent carbothermal reduction
under an 80 mbar Ar gas atmosphere. High-temperature molten salt electrolysis was introduced as an option that
enables the separation of rare earth elements from fluoride-based molten salts using produced MRDO [3]. One of
the challenges in this electrochemical approach for REE electrowinning is effective control of the anode effects to
make the electrolytic production of rare earths more environmentally friendly [3,4]. Minimizing the perfluorocarbon
compounds emission (PFC), in rare earth electrolysis, should be the primary goal, owing to their high global
warming potential [4,5].
In the present work, we investigated the off-gases emissions during the REE electrolysis from NdFeB magnet scrap
using in-situ FTIR-spectrometry, in order to understand the formation pathways of CO, CO2, and perfluorocarbon
gases (CF4 and C2F6) made at the anode. The electrolytic extraction of rare earths from fluoride-based molten salts
with different contents of MRDO present was performed using molybdenum (Mo) as a cathode, tungsten (W) as a
reference electrode, and a glassy carbon (GC) electrode as an anode. It was found that depending on the content
of the starting material, the dissolution of MRDO in their corresponding fluoride molten salts most probably induces
the formation of different oxyfluoride complexes and their subsequent reactions on the GC anode. The anode
reactions in the fluoride-based melts are, most likely, results of either oxide or fluoride formation by exchange with
the fluoride or oxide complexes present in the electrolyte. The produced oxygen subsequently reacts with carbon
to generate CO and CO2. With F− present, PFC compounds such as CF4 and C2F6 can also be formed from a GC anode.
The anode gas products are composed mainly of CO and CO2. The average CO2 concentration was approximately
450 ppm, while CO concentration was around 40 ppm. CF4 emissions in off-gas products were detected periodically,
except for some spikes, and even then, the concentration was below 4 ppm. C2F6 was not detected. The results
indicate that the electrodeposition of REE within the applied potential range occurs at the expense of their
corresponding oxides, provided by MRDO. To develop a more efficient RE recovery process, we opted for a low
deposition overpotential to suppress the emission of greenhouse gases and further enhance the control of their
emission in rare earth electrolysis.
PB  - Serbian Chemical Society
C3  - 9th Regional Symposium on Electrochemistry - South-East Europe, Book of Abstract, 3 to 7 June, 2024, Novi Sad, Serbia
T1  - Off-gases emission during the rare earth electrolysis from magnet recycling derived oxides
SP  - 123
EP  - 123
DO  - 10.5281/zenodo.11194247
ER  - 

@conference{
author = "Petrović, Nataša M. and Cvetković, Vesna. S and Prasakti, Laras and Feldhaus, Dominic and Friedrich, Bernd and Jovićević, Jovan J. and Petrović, Nataša",
year = "2024",
abstract = "In the progressive energy transition process, rare earth elements (REE) became key components in crucial products
that play a central role in the development of renewable energy and low-carbon technologies. With China currently
producing more than 90 % of the world's REE output, many of the world's economies are facing REE supply risk [1].
To address this problem, many countries need to look for alternative resources of rare earths, e.g. recycling of these
elements from REE-containing end-of-life products. A new route for recovery of REE from NdFeB magnet scrap,
using a combination of pyrometallurgical treatment of spent NdFeB magnets, and a subsequent molten salt
electrolysis process, has been investigated in the authors’ laboratory [2]. The magnet recycling derived oxides
(MRDO), were produced from spent NdFeB magnets by oxidation in air and subsequent carbothermal reduction
under an 80 mbar Ar gas atmosphere. High-temperature molten salt electrolysis was introduced as an option that
enables the separation of rare earth elements from fluoride-based molten salts using produced MRDO [3]. One of
the challenges in this electrochemical approach for REE electrowinning is effective control of the anode effects to
make the electrolytic production of rare earths more environmentally friendly [3,4]. Minimizing the perfluorocarbon
compounds emission (PFC), in rare earth electrolysis, should be the primary goal, owing to their high global
warming potential [4,5].
In the present work, we investigated the off-gases emissions during the REE electrolysis from NdFeB magnet scrap
using in-situ FTIR-spectrometry, in order to understand the formation pathways of CO, CO2, and perfluorocarbon
gases (CF4 and C2F6) made at the anode. The electrolytic extraction of rare earths from fluoride-based molten salts
with different contents of MRDO present was performed using molybdenum (Mo) as a cathode, tungsten (W) as a
reference electrode, and a glassy carbon (GC) electrode as an anode. It was found that depending on the content
of the starting material, the dissolution of MRDO in their corresponding fluoride molten salts most probably induces
the formation of different oxyfluoride complexes and their subsequent reactions on the GC anode. The anode
reactions in the fluoride-based melts are, most likely, results of either oxide or fluoride formation by exchange with
the fluoride or oxide complexes present in the electrolyte. The produced oxygen subsequently reacts with carbon
to generate CO and CO2. With F− present, PFC compounds such as CF4 and C2F6 can also be formed from a GC anode.
The anode gas products are composed mainly of CO and CO2. The average CO2 concentration was approximately
450 ppm, while CO concentration was around 40 ppm. CF4 emissions in off-gas products were detected periodically,
except for some spikes, and even then, the concentration was below 4 ppm. C2F6 was not detected. The results
indicate that the electrodeposition of REE within the applied potential range occurs at the expense of their
corresponding oxides, provided by MRDO. To develop a more efficient RE recovery process, we opted for a low
deposition overpotential to suppress the emission of greenhouse gases and further enhance the control of their
emission in rare earth electrolysis.",
publisher = "Serbian Chemical Society",
journal = "9th Regional Symposium on Electrochemistry - South-East Europe, Book of Abstract, 3 to 7 June, 2024, Novi Sad, Serbia",
title = "Off-gases emission during the rare earth electrolysis from magnet recycling derived oxides",
pages = "123-123",
doi = "10.5281/zenodo.11194247"
}

Petrović, N. M., Cvetković, Vesna. S., Prasakti, L., Feldhaus, D., Friedrich, B., Jovićević, J. J.,& Petrović, N.. (2024). Off-gases emission during the rare earth electrolysis from magnet recycling derived oxides. in 9th Regional Symposium on Electrochemistry - South-East Europe, Book of Abstract, 3 to 7 June, 2024, Novi Sad, Serbia
Serbian Chemical Society., 123-123.
https://doi.org/10.5281/zenodo.11194247

Petrović NM, Cvetković VS, Prasakti L, Feldhaus D, Friedrich B, Jovićević JJ, Petrović N. Off-gases emission during the rare earth electrolysis from magnet recycling derived oxides. in 9th Regional Symposium on Electrochemistry - South-East Europe, Book of Abstract, 3 to 7 June, 2024, Novi Sad, Serbia. 2024;:123-123.
doi:10.5281/zenodo.11194247 .

Petrović, Nataša M., Cvetković, Vesna. S, Prasakti, Laras, Feldhaus, Dominic, Friedrich, Bernd, Jovićević, Jovan J., Petrović, Nataša, "Off-gases emission during the rare earth electrolysis from magnet recycling derived oxides" in 9th Regional Symposium on Electrochemistry - South-East Europe, Book of Abstract, 3 to 7 June, 2024, Novi Sad, Serbia (2024):123-123,
https://doi.org/10.5281/zenodo.11194247 . .

TY  - CONF
AU  - Milić, Jelena
AU  - Radak, Bojan
AU  - Dunjić, Branko
PY  - 2024
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/7648
AB  - Green chemistry has emerged as a significant field in science in recent years due to
environmental concerns, the need to mitigate chemicals health hazards, regulatory
pressure, and economic benefits. This paper analyzes the trend of scientific publications on
green chemistry in Serbia over the last 10 years. For this purpose, data were retrieved from
the Scopus through a search for the study period, 2014-2024, limited to Serbia. In total, 96
records were retrieved. The results showed that green chemistry is increasingly prevalent
in different fields of knowledge in Serbia, with the highest percentages in chemistry
(22.1%), biochemistry, genetics, and molecular biology (19.1%), environmental science
(13.6%), The number of publications first peaked in 2018, decreasing in subsequent years
probably due to the COVID-19 pandemic, and then peaking again even more in 2022.
Concerning the type of publication, most publications are Articles (90.6%) and Reviews
(7.3%), with more than half affiliated with the University of Belgrade (56 documents). The
obtained results indicate that the green chemistry in Serbia is becoming more recognizable
among researchers in recent years, and it can be assumed that this interest will continue to
trend upwards.
T1  - Poster: "Green chemistry: trends in Serbia (2014-2024)"
UR  - https://hdl.handle.net/21.15107/rcub_cer_7648
ER  - 

@conference{
author = "Milić, Jelena and Radak, Bojan and Dunjić, Branko",
year = "2024",
abstract = "Green chemistry has emerged as a significant field in science in recent years due to
environmental concerns, the need to mitigate chemicals health hazards, regulatory
pressure, and economic benefits. This paper analyzes the trend of scientific publications on
green chemistry in Serbia over the last 10 years. For this purpose, data were retrieved from
the Scopus through a search for the study period, 2014-2024, limited to Serbia. In total, 96
records were retrieved. The results showed that green chemistry is increasingly prevalent
in different fields of knowledge in Serbia, with the highest percentages in chemistry
(22.1%), biochemistry, genetics, and molecular biology (19.1%), environmental science
(13.6%), The number of publications first peaked in 2018, decreasing in subsequent years
probably due to the COVID-19 pandemic, and then peaking again even more in 2022.
Concerning the type of publication, most publications are Articles (90.6%) and Reviews
(7.3%), with more than half affiliated with the University of Belgrade (56 documents). The
obtained results indicate that the green chemistry in Serbia is becoming more recognizable
among researchers in recent years, and it can be assumed that this interest will continue to
trend upwards.",
title = "Poster: "Green chemistry: trends in Serbia (2014-2024)"",
url = "https://hdl.handle.net/21.15107/rcub_cer_7648"
}

Milić, J., Radak, B.,& Dunjić, B.. (2024). Poster: "Green chemistry: trends in Serbia (2014-2024)". .
https://hdl.handle.net/21.15107/rcub_cer_7648

Milić J, Radak B, Dunjić B. Poster: "Green chemistry: trends in Serbia (2014-2024)". 2024;.
https://hdl.handle.net/21.15107/rcub_cer_7648 .

Milić, Jelena, Radak, Bojan, Dunjić, Branko, "Poster: "Green chemistry: trends in Serbia (2014-2024)"" (2024),
https://hdl.handle.net/21.15107/rcub_cer_7648 .

TY  - JOUR
AU  - Vidaković, Danijela
AU  - Dimkić, Ivica
AU  - Krizmanić, Jelena
AU  - Janakiev, Tamara
AU  - Gavrilović, Bojan
AU  - Ćirić, Miloš
PY  - 2024
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/7642
AB  - Current knowledge of the microbiota of soda pans of the Carpathian Basin focuses mainly on diatoms. In studying six
soda pans in Vojvodina (Serbia), we aimed to gain deeper insights into the diatom community by using not only traditional
microscopic analysis but also high-throughput sequencing of the 18S rRNA gene. In addition, this study aimed to evaluate
bacterial communities in these soda pans for the first time using the 16S rRNA gene marker. Although similar numbers
of diatom taxa were found using both approaches, a significant discrepancy in species composition was found. The genus
Nitzschia was one of the most represented and numerous genera according to the morphological and molecular analyses,
but with lower diversity according to the molecular data, with the sequences mostly unassigned. Another major discrepancy
was noticed with taxon Halamphora veneta, the results of metabarcoding showed high abundance in almost all soda
pans, while microscopy detected it as very low. Diverse communities of aerobic and anaerobic bacteria were detected in
the studied soda pans, such as Proteobacteria, Bacteroidota, Actinobacteria, Bacillaceae, and Peptoclostridium. According
to current knowledge, harsh environmental conditions and habitat homogeneity regulate diatom and bacteria community
composition and enable the survival of taxa with predominantly high ecophysiological plasticity. Finally, uncovering the
structure of the microbial community as the first phase in developing an efficient tool to assess the ecological status of
these fragile ecosystems is an essential step towards their conservation.
PB  - Springer
T2  - Wetlands
T1  - Diatom and Bacterial Communities in Saline Habitats (Vojvodina, Serbia)
VL  - 44
SP  - 55
DO  - 10.1007/s13157-024-01809-4
ER  - 

@article{
author = "Vidaković, Danijela and Dimkić, Ivica and Krizmanić, Jelena and Janakiev, Tamara and Gavrilović, Bojan and Ćirić, Miloš",
year = "2024",
abstract = "Current knowledge of the microbiota of soda pans of the Carpathian Basin focuses mainly on diatoms. In studying six
soda pans in Vojvodina (Serbia), we aimed to gain deeper insights into the diatom community by using not only traditional
microscopic analysis but also high-throughput sequencing of the 18S rRNA gene. In addition, this study aimed to evaluate
bacterial communities in these soda pans for the first time using the 16S rRNA gene marker. Although similar numbers
of diatom taxa were found using both approaches, a significant discrepancy in species composition was found. The genus
Nitzschia was one of the most represented and numerous genera according to the morphological and molecular analyses,
but with lower diversity according to the molecular data, with the sequences mostly unassigned. Another major discrepancy
was noticed with taxon Halamphora veneta, the results of metabarcoding showed high abundance in almost all soda
pans, while microscopy detected it as very low. Diverse communities of aerobic and anaerobic bacteria were detected in
the studied soda pans, such as Proteobacteria, Bacteroidota, Actinobacteria, Bacillaceae, and Peptoclostridium. According
to current knowledge, harsh environmental conditions and habitat homogeneity regulate diatom and bacteria community
composition and enable the survival of taxa with predominantly high ecophysiological plasticity. Finally, uncovering the
structure of the microbial community as the first phase in developing an efficient tool to assess the ecological status of
these fragile ecosystems is an essential step towards their conservation.",
publisher = "Springer",
journal = "Wetlands",
title = "Diatom and Bacterial Communities in Saline Habitats (Vojvodina, Serbia)",
volume = "44",
pages = "55",
doi = "10.1007/s13157-024-01809-4"
}

Vidaković, D., Dimkić, I., Krizmanić, J., Janakiev, T., Gavrilović, B.,& Ćirić, M.. (2024). Diatom and Bacterial Communities in Saline Habitats (Vojvodina, Serbia). in Wetlands
Springer., 44, 55.
https://doi.org/10.1007/s13157-024-01809-4

Vidaković D, Dimkić I, Krizmanić J, Janakiev T, Gavrilović B, Ćirić M. Diatom and Bacterial Communities in Saline Habitats (Vojvodina, Serbia). in Wetlands. 2024;44:55.
doi:10.1007/s13157-024-01809-4 .

Vidaković, Danijela, Dimkić, Ivica, Krizmanić, Jelena, Janakiev, Tamara, Gavrilović, Bojan, Ćirić, Miloš, "Diatom and Bacterial Communities in Saline Habitats (Vojvodina, Serbia)" in Wetlands, 44 (2024):55,
https://doi.org/10.1007/s13157-024-01809-4 . .

TY  - CONF
AU  - Košević, Milica
AU  - Nikolić, Nebojša D.
AU  - Lović, Jelena
PY  - 2024
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/7644
AB  - Electrochemistry in alkaline solution is substantial for the examination on electrooxidation of liquid fuels. Recently, alkaline direct alcohol fuel cells (ADAFCs) have shown the interest of researchers due to their advantages in performance and cost of materials, as an important characteristics for the commercialization of fuel cells. Within this context, Pdbased catalysts are attracting a great deal of attention as catalysts for the methanol oxidation reaction (MOR) in alkaline solution. Some metals may have a promoting effect on electrooxidation of alcohols and among them is antimony.
PB  - Serbian Chemical Society
C3  - Book of Abstracts, 9th Regional Symposium on Electrochemistry - South-East Europe, June 3-7, 2024, Novi Sad, Serbia
T1  - Methanol oxidation reaction on electrodeposited Pd and SbPd electrocatalysts in alkali metal hydroxide solutions
SP  - 88
EP  - 88
DO  - 10.5281/zenodo.11194247
ER  - 

@conference{
author = "Košević, Milica and Nikolić, Nebojša D. and Lović, Jelena",
year = "2024",
abstract = "Electrochemistry in alkaline solution is substantial for the examination on electrooxidation of liquid fuels. Recently, alkaline direct alcohol fuel cells (ADAFCs) have shown the interest of researchers due to their advantages in performance and cost of materials, as an important characteristics for the commercialization of fuel cells. Within this context, Pdbased catalysts are attracting a great deal of attention as catalysts for the methanol oxidation reaction (MOR) in alkaline solution. Some metals may have a promoting effect on electrooxidation of alcohols and among them is antimony.",
publisher = "Serbian Chemical Society",
journal = "Book of Abstracts, 9th Regional Symposium on Electrochemistry - South-East Europe, June 3-7, 2024, Novi Sad, Serbia",
title = "Methanol oxidation reaction on electrodeposited Pd and SbPd electrocatalysts in alkali metal hydroxide solutions",
pages = "88-88",
doi = "10.5281/zenodo.11194247"
}

Košević, M., Nikolić, N. D.,& Lović, J.. (2024). Methanol oxidation reaction on electrodeposited Pd and SbPd electrocatalysts in alkali metal hydroxide solutions. in Book of Abstracts, 9th Regional Symposium on Electrochemistry - South-East Europe, June 3-7, 2024, Novi Sad, Serbia
Serbian Chemical Society., 88-88.
https://doi.org/10.5281/zenodo.11194247

Košević M, Nikolić ND, Lović J. Methanol oxidation reaction on electrodeposited Pd and SbPd electrocatalysts in alkali metal hydroxide solutions. in Book of Abstracts, 9th Regional Symposium on Electrochemistry - South-East Europe, June 3-7, 2024, Novi Sad, Serbia. 2024;:88-88.
doi:10.5281/zenodo.11194247 .

Košević, Milica, Nikolić, Nebojša D., Lović, Jelena, "Methanol oxidation reaction on electrodeposited Pd and SbPd electrocatalysts in alkali metal hydroxide solutions" in Book of Abstracts, 9th Regional Symposium on Electrochemistry - South-East Europe, June 3-7, 2024, Novi Sad, Serbia (2024):88-88,
https://doi.org/10.5281/zenodo.11194247 . .

TY  - CONF
AU  - Nikolić, Nebojša D.
AU  - Lović, Jelena
AU  - Maksimović, Vesna
AU  - Vuković, Nikola
AU  - Stevanović, Sanja
PY  - 2024
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/7643
AB  - The alkaline electrolytes of zinc are widely used in a Zn-air secondary batteries which represent promising candidate for energy storage with many advantages relative to the other types, such as Li-air, Al-air, and Mg-air batteries. These advantages are related with an abundance of Zn, low toxicity, and low cost, as well as by the fact that Zn possess a relatively high specific energy density. One of the largest problems in a development of Zn-air batteries is dendritic growth caused by the uneven deposition of zinc in the charging process. The solving of this problem implies the good knowledge of all phenomena related with Zn deposition, and regarding it, this study aims to establish a correlation between morphology and structure of electrolytically produced Zn irregular forms, especially Zn dendrites.
PB  - Serbian Chemical Society
C3  - Book of Abstracts, 9th Regional Symposium on Electrochemistry - South-East Europe, June 3-7, 2024, Novi Sad, Serbia
T1  - Morphology and structure of electrolytically produced zinc dendrites from the alkaline electrolyte
SP  - 97
EP  - 97
DO  - 10.5281/zenodo.11194247
ER  - 

@conference{
author = "Nikolić, Nebojša D. and Lović, Jelena and Maksimović, Vesna and Vuković, Nikola and Stevanović, Sanja",
year = "2024",
abstract = "The alkaline electrolytes of zinc are widely used in a Zn-air secondary batteries which represent promising candidate for energy storage with many advantages relative to the other types, such as Li-air, Al-air, and Mg-air batteries. These advantages are related with an abundance of Zn, low toxicity, and low cost, as well as by the fact that Zn possess a relatively high specific energy density. One of the largest problems in a development of Zn-air batteries is dendritic growth caused by the uneven deposition of zinc in the charging process. The solving of this problem implies the good knowledge of all phenomena related with Zn deposition, and regarding it, this study aims to establish a correlation between morphology and structure of electrolytically produced Zn irregular forms, especially Zn dendrites.",
publisher = "Serbian Chemical Society",
journal = "Book of Abstracts, 9th Regional Symposium on Electrochemistry - South-East Europe, June 3-7, 2024, Novi Sad, Serbia",
title = "Morphology and structure of electrolytically produced zinc dendrites from the alkaline electrolyte",
pages = "97-97",
doi = "10.5281/zenodo.11194247"
}

Nikolić, N. D., Lović, J., Maksimović, V., Vuković, N.,& Stevanović, S.. (2024). Morphology and structure of electrolytically produced zinc dendrites from the alkaline electrolyte. in Book of Abstracts, 9th Regional Symposium on Electrochemistry - South-East Europe, June 3-7, 2024, Novi Sad, Serbia
Serbian Chemical Society., 97-97.
https://doi.org/10.5281/zenodo.11194247

Nikolić ND, Lović J, Maksimović V, Vuković N, Stevanović S. Morphology and structure of electrolytically produced zinc dendrites from the alkaline electrolyte. in Book of Abstracts, 9th Regional Symposium on Electrochemistry - South-East Europe, June 3-7, 2024, Novi Sad, Serbia. 2024;:97-97.
doi:10.5281/zenodo.11194247 .

Nikolić, Nebojša D., Lović, Jelena, Maksimović, Vesna, Vuković, Nikola, Stevanović, Sanja, "Morphology and structure of electrolytically produced zinc dendrites from the alkaline electrolyte" in Book of Abstracts, 9th Regional Symposium on Electrochemistry - South-East Europe, June 3-7, 2024, Novi Sad, Serbia (2024):97-97,
https://doi.org/10.5281/zenodo.11194247 . .

TY  - JOUR
AU  - Cvetković, Vesna S.
AU  - Jović, Vladimir D.
AU  - Nikolić, Nebojša D.
AU  - Barudžija, Tanja S.
AU  - Dimitrijević, Silvana B.
AU  - Jovićević, Jovan N.
PY  - 2024
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/7572
AB  - Electrodeposition of copper from deep eutectic solvents (DES) based on a mixture of choline chloride and
ethylene glycol containing CuCl2⋅2H2O at 50 ◦C and 80 ◦C was studied. Electrochemical reduction/oxidation of
Cu(II)/Cu(0) on glassy carbon (GC) and palladium (Pd) electrodes was investigated by cyclic voltammetry (CV)
and square wave voltammetry (SWV) emphasizing that this process takes place through two steps, Cu(II) ↔ Cu(I)
and Cu(I) ↔ Cu(0). The CV results showed that in chloride-rich DES electrolytes, the increased presence of chloro
ligands raises the overpotential required for Cu electrodeposition. The electrochemical impedance spectroscopy
(EIS) results indicate simultaneous electrodeposition of Cu and electrosorption of large cations on electrodeposited
Cu on both GC and Pd substrates. Scanning electron microscopy (SEM) results showed that Cu grains of
approximately 1 μm were obtained by electrodeposition of Cu on both Pd and GC, whereby better coverage by
electrodeposited Cu was obtained on Pd than on GC. Cu electrodeposited on Pd was relatively uniform and
smooth, but porous, while Cu electrodeposited on GC was dispersed in small agglomerates. Energy-dispersive Xray
spectroscopy (EDS) of Cu electrodeposited on Pd detected the dominant presence of Cu with the possibility of
the formation of CuPd alloy. The presence of CuPd alloy face-centred cubic structures is confirmed by X-ray
diffraction (XRD) along with metallic Cu.
PB  - Elsevier
T2  - Journal of Electroanalytical Chemistry
T1  - Electrodeposition of copper on glassy carbon and palladium from choline chloride - ethylene glycol deep eutectic solvent
VL  - 958
SP  - 118161
DO  - 10.1016/j.jelechem.2024.118161
ER  - 

@article{
author = "Cvetković, Vesna S. and Jović, Vladimir D. and Nikolić, Nebojša D. and Barudžija, Tanja S. and Dimitrijević, Silvana B. and Jovićević, Jovan N.",
year = "2024",
abstract = "Electrodeposition of copper from deep eutectic solvents (DES) based on a mixture of choline chloride and
ethylene glycol containing CuCl2⋅2H2O at 50 ◦C and 80 ◦C was studied. Electrochemical reduction/oxidation of
Cu(II)/Cu(0) on glassy carbon (GC) and palladium (Pd) electrodes was investigated by cyclic voltammetry (CV)
and square wave voltammetry (SWV) emphasizing that this process takes place through two steps, Cu(II) ↔ Cu(I)
and Cu(I) ↔ Cu(0). The CV results showed that in chloride-rich DES electrolytes, the increased presence of chloro
ligands raises the overpotential required for Cu electrodeposition. The electrochemical impedance spectroscopy
(EIS) results indicate simultaneous electrodeposition of Cu and electrosorption of large cations on electrodeposited
Cu on both GC and Pd substrates. Scanning electron microscopy (SEM) results showed that Cu grains of
approximately 1 μm were obtained by electrodeposition of Cu on both Pd and GC, whereby better coverage by
electrodeposited Cu was obtained on Pd than on GC. Cu electrodeposited on Pd was relatively uniform and
smooth, but porous, while Cu electrodeposited on GC was dispersed in small agglomerates. Energy-dispersive Xray
spectroscopy (EDS) of Cu electrodeposited on Pd detected the dominant presence of Cu with the possibility of
the formation of CuPd alloy. The presence of CuPd alloy face-centred cubic structures is confirmed by X-ray
diffraction (XRD) along with metallic Cu.",
publisher = "Elsevier",
journal = "Journal of Electroanalytical Chemistry",
title = "Electrodeposition of copper on glassy carbon and palladium from choline chloride - ethylene glycol deep eutectic solvent",
volume = "958",
pages = "118161",
doi = "10.1016/j.jelechem.2024.118161"
}

Cvetković, V. S., Jović, V. D., Nikolić, N. D., Barudžija, T. S., Dimitrijević, S. B.,& Jovićević, J. N.. (2024). Electrodeposition of copper on glassy carbon and palladium from choline chloride - ethylene glycol deep eutectic solvent. in Journal of Electroanalytical Chemistry
Elsevier., 958, 118161.
https://doi.org/10.1016/j.jelechem.2024.118161

Cvetković VS, Jović VD, Nikolić ND, Barudžija TS, Dimitrijević SB, Jovićević JN. Electrodeposition of copper on glassy carbon and palladium from choline chloride - ethylene glycol deep eutectic solvent. in Journal of Electroanalytical Chemistry. 2024;958:118161.
doi:10.1016/j.jelechem.2024.118161 .

Cvetković, Vesna S., Jović, Vladimir D., Nikolić, Nebojša D., Barudžija, Tanja S., Dimitrijević, Silvana B., Jovićević, Jovan N., "Electrodeposition of copper on glassy carbon and palladium from choline chloride - ethylene glycol deep eutectic solvent" in Journal of Electroanalytical Chemistry, 958 (2024):118161,
https://doi.org/10.1016/j.jelechem.2024.118161 . .

TY  - JOUR
AU  - Lukić, Marija
AU  - Avdalović, Jelena
AU  - Gojgić-Cvijović, Gordana
AU  - Žerađanin, Aleksandra
AU  - Mrazovac Kurilić, Sanja
AU  - Ilić, Mila
AU  - Miletić, Srđan
AU  - Vrvić, Miroslav
AU  - Beškoski, Vladimir
PY  - 2024
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/7584
AB  - The aim of this paper is to provide insight into research and activities of in situ remediation to remove petroleum hydrocarbon pollutants from a contaminated aquifer’s sediment, located near two radial collector wells of a water supply system. It was decided that the most appropriate method for remediation of this aquifer’s sediment is in situ bioremediation because it is clean, efficient and sustainable technology. Before the start of the bioremediation process, it was necessary to isolate and cultivate the microorganisms present at the contamination site, so they could be later applied in the bioremediation process. The samples before and after the bioremediation were studied using both GC and GC × GC–MS to determine how the concentrations of contaminants changed over time. Additionally, in this paper, a spatiotemporal representation of the change in hydrocarbon content by depth within the zone of the highest contamination over time is shown. After 12 months of bioremediation, the hydrocarbon content in the samples decreased by 82.0%, and based on GCxGC-MS analysis, the order of degradation of various hydrocarbon groups was as follows: steranes (99.6%), isoprenoids (98.4%), benzene derivatives (98.4%), alkanes (97.2%), and terpenes (49.3%). The exponential decay model showed the greatest decomposition rate of hydrocarbons occurred at depths of 8–10 m, with an average decay constant of 0.227, independent of the initial concentration of hydrocarbons. To the best of our knowledge, to date, the described approach has not been applied to an aquifer (the simultaneous treatment of groundwater and its associated sediment layers).
PB  - Springer Link
T2  - Clean Technologies and Environmental Policy
T1  - Industrial-scale bioremediation of a hydrocarbon-contaminated aquifer’s sediment at the location of a heating plant, Belgrade, Serbia
DO  - 10.1007/s10098-023-02724-8
ER  - 

@article{
author = "Lukić, Marija and Avdalović, Jelena and Gojgić-Cvijović, Gordana and Žerađanin, Aleksandra and Mrazovac Kurilić, Sanja and Ilić, Mila and Miletić, Srđan and Vrvić, Miroslav and Beškoski, Vladimir",
year = "2024",
abstract = "The aim of this paper is to provide insight into research and activities of in situ remediation to remove petroleum hydrocarbon pollutants from a contaminated aquifer’s sediment, located near two radial collector wells of a water supply system. It was decided that the most appropriate method for remediation of this aquifer’s sediment is in situ bioremediation because it is clean, efficient and sustainable technology. Before the start of the bioremediation process, it was necessary to isolate and cultivate the microorganisms present at the contamination site, so they could be later applied in the bioremediation process. The samples before and after the bioremediation were studied using both GC and GC × GC–MS to determine how the concentrations of contaminants changed over time. Additionally, in this paper, a spatiotemporal representation of the change in hydrocarbon content by depth within the zone of the highest contamination over time is shown. After 12 months of bioremediation, the hydrocarbon content in the samples decreased by 82.0%, and based on GCxGC-MS analysis, the order of degradation of various hydrocarbon groups was as follows: steranes (99.6%), isoprenoids (98.4%), benzene derivatives (98.4%), alkanes (97.2%), and terpenes (49.3%). The exponential decay model showed the greatest decomposition rate of hydrocarbons occurred at depths of 8–10 m, with an average decay constant of 0.227, independent of the initial concentration of hydrocarbons. To the best of our knowledge, to date, the described approach has not been applied to an aquifer (the simultaneous treatment of groundwater and its associated sediment layers).",
publisher = "Springer Link",
journal = "Clean Technologies and Environmental Policy",
title = "Industrial-scale bioremediation of a hydrocarbon-contaminated aquifer’s sediment at the location of a heating plant, Belgrade, Serbia",
doi = "10.1007/s10098-023-02724-8"
}

Lukić, M., Avdalović, J., Gojgić-Cvijović, G., Žerađanin, A., Mrazovac Kurilić, S., Ilić, M., Miletić, S., Vrvić, M.,& Beškoski, V.. (2024). Industrial-scale bioremediation of a hydrocarbon-contaminated aquifer’s sediment at the location of a heating plant, Belgrade, Serbia. in Clean Technologies and Environmental Policy
Springer Link..
https://doi.org/10.1007/s10098-023-02724-8

Lukić M, Avdalović J, Gojgić-Cvijović G, Žerađanin A, Mrazovac Kurilić S, Ilić M, Miletić S, Vrvić M, Beškoski V. Industrial-scale bioremediation of a hydrocarbon-contaminated aquifer’s sediment at the location of a heating plant, Belgrade, Serbia. in Clean Technologies and Environmental Policy. 2024;.
doi:10.1007/s10098-023-02724-8 .

Lukić, Marija, Avdalović, Jelena, Gojgić-Cvijović, Gordana, Žerađanin, Aleksandra, Mrazovac Kurilić, Sanja, Ilić, Mila, Miletić, Srđan, Vrvić, Miroslav, Beškoski, Vladimir, "Industrial-scale bioremediation of a hydrocarbon-contaminated aquifer’s sediment at the location of a heating plant, Belgrade, Serbia" in Clean Technologies and Environmental Policy (2024),
https://doi.org/10.1007/s10098-023-02724-8 . .

TY  - JOUR
AU  - Popović, Marko
AU  - Popović, Marta
AU  - Šekularac, Gavrilo
AU  - Pantović Pavlović, Marijana
PY  - 2024
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/7620
AB  - All genome sequences and associated metadata in this dataset are published
in GISAID’s EpiCoV database. To view the contributors of each individual
sequence with details such as accession number, Virus name, Collection date,
Originating Lab and Submitting Lab and the list of Authors, visit
10.55876/gis8.230924yd
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Supplementary material to Omicron BA.2.86 Pirola nightmare: Empirical formulas and thermodynamic properties (enthalpy, entropy and Gibbs energy) of nucleocapsid, virus particle and biosynthesis of BA.2.86 Pirola variant of SARS-CoV-2
DO  - 10.2298/JSC240322051P
ER  - 

@article{
author = "Popović, Marko and Popović, Marta and Šekularac, Gavrilo and Pantović Pavlović, Marijana",
year = "2024",
abstract = "All genome sequences and associated metadata in this dataset are published
in GISAID’s EpiCoV database. To view the contributors of each individual
sequence with details such as accession number, Virus name, Collection date,
Originating Lab and Submitting Lab and the list of Authors, visit
10.55876/gis8.230924yd",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Supplementary material to Omicron BA.2.86 Pirola nightmare: Empirical formulas and thermodynamic properties (enthalpy, entropy and Gibbs energy) of nucleocapsid, virus particle and biosynthesis of BA.2.86 Pirola variant of SARS-CoV-2",
doi = "10.2298/JSC240322051P"
}

Popović, M., Popović, M., Šekularac, G.,& Pantović Pavlović, M.. (2024). Supplementary material to Omicron BA.2.86 Pirola nightmare: Empirical formulas and thermodynamic properties (enthalpy, entropy and Gibbs energy) of nucleocapsid, virus particle and biosynthesis of BA.2.86 Pirola variant of SARS-CoV-2. in Journal of the Serbian Chemical Society
Serbian Chemical Society..
https://doi.org/10.2298/JSC240322051P

Popović M, Popović M, Šekularac G, Pantović Pavlović M. Supplementary material to Omicron BA.2.86 Pirola nightmare: Empirical formulas and thermodynamic properties (enthalpy, entropy and Gibbs energy) of nucleocapsid, virus particle and biosynthesis of BA.2.86 Pirola variant of SARS-CoV-2. in Journal of the Serbian Chemical Society. 2024;.
doi:10.2298/JSC240322051P .

Popović, Marko, Popović, Marta, Šekularac, Gavrilo, Pantović Pavlović, Marijana, "Supplementary material to Omicron BA.2.86 Pirola nightmare: Empirical formulas and thermodynamic properties (enthalpy, entropy and Gibbs energy) of nucleocapsid, virus particle and biosynthesis of BA.2.86 Pirola variant of SARS-CoV-2" in Journal of the Serbian Chemical Society (2024),
https://doi.org/10.2298/JSC240322051P . .

TY  - JOUR
AU  - Radoičić, Aleksandra
AU  - Šegan, Sandra
AU  - Dramićanin, Aleksandra
AU  - Milojković-Opsenica, Dušanka
PY  - 2024
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/7609
AB  - For a long time, Reversed-Phase Liquid Chromatography (RPLC) was the most dominant
technique for the analysis of pharmaceutical compounds, but with poor efficiency in the separation of
small polar molecules. From the efforts to solve the problem of insufficient retention of these molecules,
during the last decades, a mode of liquid chromatography named Hydrophilic Interaction Liquid
Chromatography (HILIC) has experienced vast expansion. It is based on the use of a highly hydrophilic
stationary phase along with an aqueous mobile phase with high organic modifier content. In
this review, the characteristics of stationary and mobile phases used in HILIC are described, and corresponding
separation mechanisms are discussed. An overview of recently published papers dealing
with the application of HILIC in analyzing pharmaceuticals in biological and non-biological samples
is provided. Besides, the application of HILIC systems in the determination of the physicochemical
properties of compounds is described.
PB  - Bentham Science Publishers
T2  - Current Analytical Chemistry
T1  - Hydrophilic Interaction Liquid Chromatography for the Analysis of Pharmaceutical Formulations
VL  - 20
IS  - 5
SP  - 295
EP  - 317
DO  - 10.2174/0115734110290557240305045032
ER  - 

@article{
author = "Radoičić, Aleksandra and Šegan, Sandra and Dramićanin, Aleksandra and Milojković-Opsenica, Dušanka",
year = "2024",
abstract = "For a long time, Reversed-Phase Liquid Chromatography (RPLC) was the most dominant
technique for the analysis of pharmaceutical compounds, but with poor efficiency in the separation of
small polar molecules. From the efforts to solve the problem of insufficient retention of these molecules,
during the last decades, a mode of liquid chromatography named Hydrophilic Interaction Liquid
Chromatography (HILIC) has experienced vast expansion. It is based on the use of a highly hydrophilic
stationary phase along with an aqueous mobile phase with high organic modifier content. In
this review, the characteristics of stationary and mobile phases used in HILIC are described, and corresponding
separation mechanisms are discussed. An overview of recently published papers dealing
with the application of HILIC in analyzing pharmaceuticals in biological and non-biological samples
is provided. Besides, the application of HILIC systems in the determination of the physicochemical
properties of compounds is described.",
publisher = "Bentham Science Publishers",
journal = "Current Analytical Chemistry",
title = "Hydrophilic Interaction Liquid Chromatography for the Analysis of Pharmaceutical Formulations",
volume = "20",
number = "5",
pages = "295-317",
doi = "10.2174/0115734110290557240305045032"
}

Radoičić, A., Šegan, S., Dramićanin, A.,& Milojković-Opsenica, D.. (2024). Hydrophilic Interaction Liquid Chromatography for the Analysis of Pharmaceutical Formulations. in Current Analytical Chemistry
Bentham Science Publishers., 20(5), 295-317.
https://doi.org/10.2174/0115734110290557240305045032

Radoičić A, Šegan S, Dramićanin A, Milojković-Opsenica D. Hydrophilic Interaction Liquid Chromatography for the Analysis of Pharmaceutical Formulations. in Current Analytical Chemistry. 2024;20(5):295-317.
doi:10.2174/0115734110290557240305045032 .

Radoičić, Aleksandra, Šegan, Sandra, Dramićanin, Aleksandra, Milojković-Opsenica, Dušanka, "Hydrophilic Interaction Liquid Chromatography for the Analysis of Pharmaceutical Formulations" in Current Analytical Chemistry, 20, no. 5 (2024):295-317,
https://doi.org/10.2174/0115734110290557240305045032 . .

TY  - CONF
AU  - Marinković, Dalibor
AU  - Nikolić, Daliborka
AU  - Seidel, Carsten
AU  - Seidel-Morgenstern, Andreas
AU  - Kienle, Achim
AU  - Petkovska, Menka
PY  - 2024
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/7522
AB  - The continuous industrial chemical processes are typically designed through steady-state conditions. Nevertheless, there is evidence that processes can be intensified by applying optimized forced periodic operation. Possible improvements in reactor performances caused by the implementation of forced periodic operation (FPO) can be successfully evaluated by applying a nonlinear frequency response (NFR) analysis, before experimental investigation. In this study, we will present the results of two case studies based on heterogeneously catalyzed methanol synthesis in a continuous stirred tank reactor (CSTR). The first is an isothermal case, and the second is a more complicated and more realistic, non-isothermal case.
PB  - Stockholm, Sweden : Scanditale AB
C3  - Energy Proceedings
T1  - Evaluation of possible improvements of forced periodically operated reactor in which methanol synthesis takes place – based on the Nonlinear Frequency Response analysis
VL  - 43
IS  - VI
DO  - 10.46855/energy-proceedings-11025
ER  - 

@conference{
author = "Marinković, Dalibor and Nikolić, Daliborka and Seidel, Carsten and Seidel-Morgenstern, Andreas and Kienle, Achim and Petkovska, Menka",
year = "2024",
abstract = "The continuous industrial chemical processes are typically designed through steady-state conditions. Nevertheless, there is evidence that processes can be intensified by applying optimized forced periodic operation. Possible improvements in reactor performances caused by the implementation of forced periodic operation (FPO) can be successfully evaluated by applying a nonlinear frequency response (NFR) analysis, before experimental investigation. In this study, we will present the results of two case studies based on heterogeneously catalyzed methanol synthesis in a continuous stirred tank reactor (CSTR). The first is an isothermal case, and the second is a more complicated and more realistic, non-isothermal case.",
publisher = "Stockholm, Sweden : Scanditale AB",
journal = "Energy Proceedings",
title = "Evaluation of possible improvements of forced periodically operated reactor in which methanol synthesis takes place – based on the Nonlinear Frequency Response analysis",
volume = "43",
number = "VI",
doi = "10.46855/energy-proceedings-11025"
}

Marinković, D., Nikolić, D., Seidel, C., Seidel-Morgenstern, A., Kienle, A.,& Petkovska, M.. (2024). Evaluation of possible improvements of forced periodically operated reactor in which methanol synthesis takes place – based on the Nonlinear Frequency Response analysis. in Energy Proceedings
Stockholm, Sweden : Scanditale AB., 43(VI).
https://doi.org/10.46855/energy-proceedings-11025

Marinković D, Nikolić D, Seidel C, Seidel-Morgenstern A, Kienle A, Petkovska M. Evaluation of possible improvements of forced periodically operated reactor in which methanol synthesis takes place – based on the Nonlinear Frequency Response analysis. in Energy Proceedings. 2024;43(VI).
doi:10.46855/energy-proceedings-11025 .

Marinković, Dalibor, Nikolić, Daliborka, Seidel, Carsten, Seidel-Morgenstern, Andreas, Kienle, Achim, Petkovska, Menka, "Evaluation of possible improvements of forced periodically operated reactor in which methanol synthesis takes place – based on the Nonlinear Frequency Response analysis" in Energy Proceedings, 43, no. VI (2024),
https://doi.org/10.46855/energy-proceedings-11025 . .

TY  - JOUR
AU  - Popović, Marko
AU  - Popović, Marta
AU  - Šekularac, Gavrilo
AU  - Pantović Pavlović, Marijana
PY  - 2024
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/7619
AB  - Similarly to a phoenix, SARS-CoV-2 has appeared periodically in waves. The new variants that appeared through mutations have suppressed earlier variants, causing new waves of the pandemic. The Omicron BA.2.86 Pirola variant is the latest in the sequence. An increased infectivity was noticed, which results in rapid spreading, as well as decreased pathogenicity, which results in a lower number of severe cases. However, in the public there is a fear of further development of the epidemic. This analysis was made with the goal to assess the risks in the period of early 2024. Mutations that were developed by the BA.2.86 variant have led to a change in empirical formula and thermodynamic properties. The empirical formula of the BA.2.86 virus particle is CH1.639023O0.284130N0.230031P0.006440S0.003765. It is different than those of other variants of SARS-CoV-2, other virus species and cellular organisms. The driving force for virus multiplication, Gibbs energy of biosynthesis, of the BA.2.86 variant is -221.75 kJ C-mol-1. It is more negative than that of its host tissue. According to the biosynthesis phenomenological equation, the more negative Gibbs energy of biosynthesis allows the virus to achieve a greater biosynthesis rate and hijack the host cell metabolism. However, Gibbs energy of biosynthesis of the BA.2.86 variant is similar to those of the CH.1.1 and XBB.1.16 variants. This means that these variants should have similar multiplications rates and thus similar pathogenicity. Therefore, it seems that there is no ground for fear of an extensive spreading of severe forms, but there are reasons for caution and monitoring of the spreading of the epidemic and potential appearance of new mutations. Moreover, unlike the earlier pandemic waves, during the newest pandemic wave, infections with influenza, RSV and BA.2.86 variant simultaneously appeared, which deserves an analysis.
AB  - Слично фениксу, SARS-CoV-2 се периодично појављивао у таласима. Нове варијанте
које су се појавиле кроз мутације потиснуле су раније варијанте, што је изазвало нове таласе
пандемије. Омикрон BA.2.86 Пирола варијанта је најновија у низу. Уочена је повећана
инфективност, што резултира брзим ширењем, као и смањена патогеност, што резултира
мањим бројем тешких случајева. Међутим, у јавности постоји страх од даљег развоја
епидемије. Ова анализа је урађена са циљем да се процене ризици у периоду од почетка
2024. године. Мутације које је развила варијанта BA.2.86 довеле су до промене емпиријске
формуле и термодинамичких особина. Емпиријска формула BA.2.86 вирусне честице је
CH1.639023O0.284130N0.230031P0.006440S0.003765. Она се разликује се од других варијанти SARS-CoV-2,
других врста вируса и ћелијских организама. Driving force за умножавање вируса, Гибсова
енергија биосинтезе, варијанте BA.2.86 је -221,75 kJ C-mol-1. Она је негативнија од Гибсове
енергије биосинтезе ткива домаћина. Према феноменолошкој једначини биосинтезе,
негативнија Гибсова енергија биосинтезе омогућава вирусу да постигне већу брзину
биосинтезе и преузме метаболизам ћелије домаћина. Међутим, Гибсова енергија
биосинтезе варијанте BA.2.86 је слична оној код варијанти CH.1.1 и XBB.1.16. То значи да
ове варијанте треба да имају сличне брзине размножавања, а самим тим и сличну
патогеност. Дакле, чини се да нема основа за страх од екстензивног ширења тешких облика,
али постоје разлози за опрез и праћење ширења епидемије и потенцијалне појаве нових
мутација. Штавише, за разлику од ранијих пандемијских таласа, током најновијег
пандемијског таласа, истовремено су се појавиле инфекције инфлуенце, RSV и варијанте
BA.2.86, што заслужује анализу.
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Omicron BA.2.86 Pirola nightmare: Empirical formulas and thermodynamic properties (enthalpy, entropy and Gibbs energy) of nucleocapsid, virus particle and biosynthesis of BA.2.86 Pirola variant of SARS-CoV-2
T1  - ОМИКРОН BA.2.86 ПИРОЛА НОЋНА МОРА: ЕМПИРИЈСКЕ ФОРМУЛЕ И ТЕРМОДИНАМИЧКЕ ОСОБИНЕ (ЕНТАЛПИЈА, ЕНТРОПИЈА И ГИБСОВА ЕНЕРГИЈА) НУКЛЕОКАПСИДА, ВИРУСНЕ ЧЕСТИЦЕ И БИОСИНТЕЗЕ BA.2.86 ПИРОЛА ВАРИЈАНТЕ
DO  - 10.2298/JSC240322051P
ER  - 

@article{
author = "Popović, Marko and Popović, Marta and Šekularac, Gavrilo and Pantović Pavlović, Marijana",
year = "2024",
abstract = "Similarly to a phoenix, SARS-CoV-2 has appeared periodically in waves. The new variants that appeared through mutations have suppressed earlier variants, causing new waves of the pandemic. The Omicron BA.2.86 Pirola variant is the latest in the sequence. An increased infectivity was noticed, which results in rapid spreading, as well as decreased pathogenicity, which results in a lower number of severe cases. However, in the public there is a fear of further development of the epidemic. This analysis was made with the goal to assess the risks in the period of early 2024. Mutations that were developed by the BA.2.86 variant have led to a change in empirical formula and thermodynamic properties. The empirical formula of the BA.2.86 virus particle is CH1.639023O0.284130N0.230031P0.006440S0.003765. It is different than those of other variants of SARS-CoV-2, other virus species and cellular organisms. The driving force for virus multiplication, Gibbs energy of biosynthesis, of the BA.2.86 variant is -221.75 kJ C-mol-1. It is more negative than that of its host tissue. According to the biosynthesis phenomenological equation, the more negative Gibbs energy of biosynthesis allows the virus to achieve a greater biosynthesis rate and hijack the host cell metabolism. However, Gibbs energy of biosynthesis of the BA.2.86 variant is similar to those of the CH.1.1 and XBB.1.16 variants. This means that these variants should have similar multiplications rates and thus similar pathogenicity. Therefore, it seems that there is no ground for fear of an extensive spreading of severe forms, but there are reasons for caution and monitoring of the spreading of the epidemic and potential appearance of new mutations. Moreover, unlike the earlier pandemic waves, during the newest pandemic wave, infections with influenza, RSV and BA.2.86 variant simultaneously appeared, which deserves an analysis., Слично фениксу, SARS-CoV-2 се периодично појављивао у таласима. Нове варијанте
које су се појавиле кроз мутације потиснуле су раније варијанте, што је изазвало нове таласе
пандемије. Омикрон BA.2.86 Пирола варијанта је најновија у низу. Уочена је повећана
инфективност, што резултира брзим ширењем, као и смањена патогеност, што резултира
мањим бројем тешких случајева. Међутим, у јавности постоји страх од даљег развоја
епидемије. Ова анализа је урађена са циљем да се процене ризици у периоду од почетка
2024. године. Мутације које је развила варијанта BA.2.86 довеле су до промене емпиријске
формуле и термодинамичких особина. Емпиријска формула BA.2.86 вирусне честице је
CH1.639023O0.284130N0.230031P0.006440S0.003765. Она се разликује се од других варијанти SARS-CoV-2,
других врста вируса и ћелијских организама. Driving force за умножавање вируса, Гибсова
енергија биосинтезе, варијанте BA.2.86 је -221,75 kJ C-mol-1. Она је негативнија од Гибсове
енергије биосинтезе ткива домаћина. Према феноменолошкој једначини биосинтезе,
негативнија Гибсова енергија биосинтезе омогућава вирусу да постигне већу брзину
биосинтезе и преузме метаболизам ћелије домаћина. Међутим, Гибсова енергија
биосинтезе варијанте BA.2.86 је слична оној код варијанти CH.1.1 и XBB.1.16. То значи да
ове варијанте треба да имају сличне брзине размножавања, а самим тим и сличну
патогеност. Дакле, чини се да нема основа за страх од екстензивног ширења тешких облика,
али постоје разлози за опрез и праћење ширења епидемије и потенцијалне појаве нових
мутација. Штавише, за разлику од ранијих пандемијских таласа, током најновијег
пандемијског таласа, истовремено су се појавиле инфекције инфлуенце, RSV и варијанте
BA.2.86, што заслужује анализу.",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Omicron BA.2.86 Pirola nightmare: Empirical formulas and thermodynamic properties (enthalpy, entropy and Gibbs energy) of nucleocapsid, virus particle and biosynthesis of BA.2.86 Pirola variant of SARS-CoV-2, ОМИКРОН BA.2.86 ПИРОЛА НОЋНА МОРА: ЕМПИРИЈСКЕ ФОРМУЛЕ И ТЕРМОДИНАМИЧКЕ ОСОБИНЕ (ЕНТАЛПИЈА, ЕНТРОПИЈА И ГИБСОВА ЕНЕРГИЈА) НУКЛЕОКАПСИДА, ВИРУСНЕ ЧЕСТИЦЕ И БИОСИНТЕЗЕ BA.2.86 ПИРОЛА ВАРИЈАНТЕ",
doi = "10.2298/JSC240322051P"
}

Popović, M., Popović, M., Šekularac, G.,& Pantović Pavlović, M.. (2024). Omicron BA.2.86 Pirola nightmare: Empirical formulas and thermodynamic properties (enthalpy, entropy and Gibbs energy) of nucleocapsid, virus particle and biosynthesis of BA.2.86 Pirola variant of SARS-CoV-2. in Journal of the Serbian Chemical Society
Serbian Chemical Society..
https://doi.org/10.2298/JSC240322051P

Popović M, Popović M, Šekularac G, Pantović Pavlović M. Omicron BA.2.86 Pirola nightmare: Empirical formulas and thermodynamic properties (enthalpy, entropy and Gibbs energy) of nucleocapsid, virus particle and biosynthesis of BA.2.86 Pirola variant of SARS-CoV-2. in Journal of the Serbian Chemical Society. 2024;.
doi:10.2298/JSC240322051P .

Popović, Marko, Popović, Marta, Šekularac, Gavrilo, Pantović Pavlović, Marijana, "Omicron BA.2.86 Pirola nightmare: Empirical formulas and thermodynamic properties (enthalpy, entropy and Gibbs energy) of nucleocapsid, virus particle and biosynthesis of BA.2.86 Pirola variant of SARS-CoV-2" in Journal of the Serbian Chemical Society (2024),
https://doi.org/10.2298/JSC240322051P . .

TY  - JOUR
AU  - Radić, Nenad
AU  - Ilić, Mila
AU  - Stojadinović, Stevan
AU  - Milić, Jelena
AU  - Avdalović, Jelena
AU  - Šaponjić, Zoran
PY  - 2024
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/7515
AB  - The plasma electrolytic oxidation process of Ti foil in the presence of a colloidal solution of Ag nanoparticles was used for the synthesis of exceptionally photocatalytically active Ag-doped TiO2 coatings. UV–Vis absorption spectroscopy was applied to follow the changes in the surface plasmon resonance band of the Ag nanoparticles as a function of the Ag:PO43− ratio in a phosphate-based electrolyte solution. Transmission electron microscopy revealed the size of the Ag nanoparticles in the range of 3–12 nm. The XRD patterns of the Ag-doped TiO2 coatings confirmed the crystalline anatase TiO2 phase regardless of the dopant concentration and without metallic Ag or crystalline Ag oxide forms. The typical porous morphology of the Ag–TiO2 coatings was observed by scanning electron microscopy. A significantly improved photocatalytic activity of the Ag–TiO2 coatings in the degradation process of the insecticide lindane (gamma isomer of benzene hexachloride) and test molecule methyl orange compared to pure TiO2 was determined using the GC technique. The degradation efficiency of Ag-doped TiO2 coatings is higher for lindane than for methyl orange.
PB  - Elsevier
T2  - Journal of Physics and Chemistry of Solids
T1  - Photocatalytically active Ag-doped TiO2 coatings developed by plasma electrolytic oxidation in the presence of colloidal Ag nanoparticles
VL  - 188
SP  - 111918
DO  - 10.1016/j.jpcs.2024.111918
ER  - 

@article{
author = "Radić, Nenad and Ilić, Mila and Stojadinović, Stevan and Milić, Jelena and Avdalović, Jelena and Šaponjić, Zoran",
year = "2024",
abstract = "The plasma electrolytic oxidation process of Ti foil in the presence of a colloidal solution of Ag nanoparticles was used for the synthesis of exceptionally photocatalytically active Ag-doped TiO2 coatings. UV–Vis absorption spectroscopy was applied to follow the changes in the surface plasmon resonance band of the Ag nanoparticles as a function of the Ag:PO43− ratio in a phosphate-based electrolyte solution. Transmission electron microscopy revealed the size of the Ag nanoparticles in the range of 3–12 nm. The XRD patterns of the Ag-doped TiO2 coatings confirmed the crystalline anatase TiO2 phase regardless of the dopant concentration and without metallic Ag or crystalline Ag oxide forms. The typical porous morphology of the Ag–TiO2 coatings was observed by scanning electron microscopy. A significantly improved photocatalytic activity of the Ag–TiO2 coatings in the degradation process of the insecticide lindane (gamma isomer of benzene hexachloride) and test molecule methyl orange compared to pure TiO2 was determined using the GC technique. The degradation efficiency of Ag-doped TiO2 coatings is higher for lindane than for methyl orange.",
publisher = "Elsevier",
journal = "Journal of Physics and Chemistry of Solids",
title = "Photocatalytically active Ag-doped TiO2 coatings developed by plasma electrolytic oxidation in the presence of colloidal Ag nanoparticles",
volume = "188",
pages = "111918",
doi = "10.1016/j.jpcs.2024.111918"
}

Radić, N., Ilić, M., Stojadinović, S., Milić, J., Avdalović, J.,& Šaponjić, Z.. (2024). Photocatalytically active Ag-doped TiO2 coatings developed by plasma electrolytic oxidation in the presence of colloidal Ag nanoparticles. in Journal of Physics and Chemistry of Solids
Elsevier., 188, 111918.
https://doi.org/10.1016/j.jpcs.2024.111918

Radić N, Ilić M, Stojadinović S, Milić J, Avdalović J, Šaponjić Z. Photocatalytically active Ag-doped TiO2 coatings developed by plasma electrolytic oxidation in the presence of colloidal Ag nanoparticles. in Journal of Physics and Chemistry of Solids. 2024;188:111918.
doi:10.1016/j.jpcs.2024.111918 .

Radić, Nenad, Ilić, Mila, Stojadinović, Stevan, Milić, Jelena, Avdalović, Jelena, Šaponjić, Zoran, "Photocatalytically active Ag-doped TiO2 coatings developed by plasma electrolytic oxidation in the presence of colloidal Ag nanoparticles" in Journal of Physics and Chemistry of Solids, 188 (2024):111918,
https://doi.org/10.1016/j.jpcs.2024.111918 . .

TY  - JOUR
AU  - Milić, Jelena
AU  - Šolević Knudsen, Tatjana
AU  - Kojić, Ivan
AU  - Avdalović, Jelena
AU  - Ilić, Mila
AU  - Vrvić, Miroslav
PY  - 2024
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/7608
AB  - The use of fossil fuels leads to environmental contamination during their extraction, processing and distribution. Microbial biodegradation provides a sustainable method for cleaning contaminated areas which follows the principles of sustainability. This paper presents the dynamics of biodegradation of hydrocarbon fractions of diesel oil, using Planomicrobium sp. and Rhodococcus sp. isolated from petroleum-contaminated sites. GC– MS analysis was employed to analyse abundances of the specific compounds such as n-alkanes, isoprenoids, sesquitepranes,
hopanes, steranes and aromatic compounds (naphthalene and its methylated homologues, phenanthrene and anthracene and their methylated homologues, and dibenzothiophene and its methylated homologues). The obtained results showed that after 30 days of biodegradation of diesel, a significant degradation was achieved, with almost complete degradation of n-alkanes and a decrease in the amount of sesquiterapanes. Rhodococcus sp. had
a higher efficiency in degradation of n-alkanes, while Planomicrobium sp. had a higher efficiency in the degradation of branched hydrocarbons. Both strains showed high activity in the biodegradation of sesquitepranes and demonstrate ability to degrade methylated phenanthrenes. Additionally, dimethyldibenzothiophenes
were almost completely degraded and removed from the system. This study presents the first comprehensive report on the GC–MS analysis of the diesel biodegradation pattern of the Planomicrobium sp., compared with the well-established Rhodococcus sp.
PB  - Taylor & Francis
T2  - Chemistry and Ecology
T1  - Short-term study of biological degradation of diesel oil by bacteria isolated from petroleum- contaminated soil
DO  - 10.1080/02757540.2024.2356565
ER  - 

@article{
author = "Milić, Jelena and Šolević Knudsen, Tatjana and Kojić, Ivan and Avdalović, Jelena and Ilić, Mila and Vrvić, Miroslav",
year = "2024",
abstract = "The use of fossil fuels leads to environmental contamination during their extraction, processing and distribution. Microbial biodegradation provides a sustainable method for cleaning contaminated areas which follows the principles of sustainability. This paper presents the dynamics of biodegradation of hydrocarbon fractions of diesel oil, using Planomicrobium sp. and Rhodococcus sp. isolated from petroleum-contaminated sites. GC– MS analysis was employed to analyse abundances of the specific compounds such as n-alkanes, isoprenoids, sesquitepranes,
hopanes, steranes and aromatic compounds (naphthalene and its methylated homologues, phenanthrene and anthracene and their methylated homologues, and dibenzothiophene and its methylated homologues). The obtained results showed that after 30 days of biodegradation of diesel, a significant degradation was achieved, with almost complete degradation of n-alkanes and a decrease in the amount of sesquiterapanes. Rhodococcus sp. had
a higher efficiency in degradation of n-alkanes, while Planomicrobium sp. had a higher efficiency in the degradation of branched hydrocarbons. Both strains showed high activity in the biodegradation of sesquitepranes and demonstrate ability to degrade methylated phenanthrenes. Additionally, dimethyldibenzothiophenes
were almost completely degraded and removed from the system. This study presents the first comprehensive report on the GC–MS analysis of the diesel biodegradation pattern of the Planomicrobium sp., compared with the well-established Rhodococcus sp.",
publisher = "Taylor & Francis",
journal = "Chemistry and Ecology",
title = "Short-term study of biological degradation of diesel oil by bacteria isolated from petroleum- contaminated soil",
doi = "10.1080/02757540.2024.2356565"
}

Milić, J., Šolević Knudsen, T., Kojić, I., Avdalović, J., Ilić, M.,& Vrvić, M.. (2024). Short-term study of biological degradation of diesel oil by bacteria isolated from petroleum- contaminated soil. in Chemistry and Ecology
Taylor & Francis..
https://doi.org/10.1080/02757540.2024.2356565

Milić J, Šolević Knudsen T, Kojić I, Avdalović J, Ilić M, Vrvić M. Short-term study of biological degradation of diesel oil by bacteria isolated from petroleum- contaminated soil. in Chemistry and Ecology. 2024;.
doi:10.1080/02757540.2024.2356565 .

Milić, Jelena, Šolević Knudsen, Tatjana, Kojić, Ivan, Avdalović, Jelena, Ilić, Mila, Vrvić, Miroslav, "Short-term study of biological degradation of diesel oil by bacteria isolated from petroleum- contaminated soil" in Chemistry and Ecology (2024),
https://doi.org/10.1080/02757540.2024.2356565 . .

TY  - JOUR
AU  - Šalipur, Hristina
AU  - Fronczak, Maciej
AU  - Prašnikar, Anže
AU  - Kamal, Khaja Mohaideen
AU  - Mudrinić, Tihana
AU  - Hadnađev-Kostić, Milica
AU  - Likozar, Blaž
AU  - Dostanić, Jasmina
AU  - Lončarević, Davor
PY  - 2024
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/7610
AB  - The concept of photocatalytic CO2 and H2O conversion to solar fuels and value-added products provides simultaneous solution for increased energy demands and environmental problems. However, the lack of efficient photocatalysts restrains the large-scale development of photocatalytic technology. In the present study, noble (Pt and Au) and transition metal (Ni) doped nanoflakes assembled on TiO2@carbon microrods with high surface area and rutile crystal structure is prepared via fast, versatile solvothermal method. The photocatalytic performance of the prepared nanocomposites was evaluated in two photocatalytic systems: CO2 reduction and hydrogen production via photoreforming. Pt-doped catalyst showed enhanced hydrogen production efficiency and increased CH4 selectivity, while Ni-doped catalyst exhibited remarkable CO2 reduction activity with higher selectivity towards CO. The mechanism of Pt-promoted CH4 formation and Ni- and Au-promoted CO formation was thoroughly discussed regarding kinetic and thermodynamic parameters.
PB  - Elsevier
T2  - Catalysis Today
T1  - Metal doped TiO2 decorated carbon nanostructured materials as an emerging photocatalysts for solar fuels production
VL  - 436
SP  - 114724
DO  - 10.1016/j.cattod.2024.114724
ER  - 

@article{
author = "Šalipur, Hristina and Fronczak, Maciej and Prašnikar, Anže and Kamal, Khaja Mohaideen and Mudrinić, Tihana and Hadnađev-Kostić, Milica and Likozar, Blaž and Dostanić, Jasmina and Lončarević, Davor",
year = "2024",
abstract = "The concept of photocatalytic CO2 and H2O conversion to solar fuels and value-added products provides simultaneous solution for increased energy demands and environmental problems. However, the lack of efficient photocatalysts restrains the large-scale development of photocatalytic technology. In the present study, noble (Pt and Au) and transition metal (Ni) doped nanoflakes assembled on TiO2@carbon microrods with high surface area and rutile crystal structure is prepared via fast, versatile solvothermal method. The photocatalytic performance of the prepared nanocomposites was evaluated in two photocatalytic systems: CO2 reduction and hydrogen production via photoreforming. Pt-doped catalyst showed enhanced hydrogen production efficiency and increased CH4 selectivity, while Ni-doped catalyst exhibited remarkable CO2 reduction activity with higher selectivity towards CO. The mechanism of Pt-promoted CH4 formation and Ni- and Au-promoted CO formation was thoroughly discussed regarding kinetic and thermodynamic parameters.",
publisher = "Elsevier",
journal = "Catalysis Today",
title = "Metal doped TiO2 decorated carbon nanostructured materials as an emerging photocatalysts for solar fuels production",
volume = "436",
pages = "114724",
doi = "10.1016/j.cattod.2024.114724"
}

Šalipur, H., Fronczak, M., Prašnikar, A., Kamal, K. M., Mudrinić, T., Hadnađev-Kostić, M., Likozar, B., Dostanić, J.,& Lončarević, D.. (2024). Metal doped TiO2 decorated carbon nanostructured materials as an emerging photocatalysts for solar fuels production. in Catalysis Today
Elsevier., 436, 114724.
https://doi.org/10.1016/j.cattod.2024.114724

Šalipur H, Fronczak M, Prašnikar A, Kamal KM, Mudrinić T, Hadnađev-Kostić M, Likozar B, Dostanić J, Lončarević D. Metal doped TiO2 decorated carbon nanostructured materials as an emerging photocatalysts for solar fuels production. in Catalysis Today. 2024;436:114724.
doi:10.1016/j.cattod.2024.114724 .

Šalipur, Hristina, Fronczak, Maciej, Prašnikar, Anže, Kamal, Khaja Mohaideen, Mudrinić, Tihana, Hadnađev-Kostić, Milica, Likozar, Blaž, Dostanić, Jasmina, Lončarević, Davor, "Metal doped TiO2 decorated carbon nanostructured materials as an emerging photocatalysts for solar fuels production" in Catalysis Today, 436 (2024):114724,
https://doi.org/10.1016/j.cattod.2024.114724 . .

TY  - JOUR
AU  - Tančić, Pavle
AU  - Milošević, Maja
AU  - Spahić, Darko
AU  - Kostić, Bojan
AU  - Kremenović, Aleksandar
AU  - Poznanović-Spahić, Maja
AU  - Kovačević, Jovan
PY  - 2024
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/6913
AB  - Five celestine crystals are sampled from the (paleo)surface intervening between the late Miocene to Pleistocene basaltic sequences of the Jabal Eghei(Nuqay) volcanic province (southern Libya). The celestine specimens are characterized by applying the combination of the SEM-WDS, ICP/OES, XRPD, and IR methods. The celestine minerals are further analyzed for their color variations and minerogenetic framework. Three samples have greenish-blue-to-blue (480.4-482.5 nm), whereas the other two samples have blue-green color (cyan; 489.1-494.1 nm). The color purity ranges from 1.36-7.16. Their similarity of chemical content is fitting into the celestine near-end members, in which exclusively 1.6-4.1 at. % of Sr2+ content was substituted by Pb2+ (0.7-0.9 at. %), Ba2+ (0.5-0.7 at. %) and Ca2+ (0.2-0.8 at. %). The composition includes vacancies ranging from 1.0 to 1.9 at. % (observed only in three samples). The content of other chemical elements is minor. The resulting unit-cell parameters have the following ranges: a0=8.3578(9)-8.3705(6) Å; b0=5.3510(5)-5.3568(4) Å; c0=6.8683(7)-6.8767(2) Å and V0=307.17(5)-308.34(4) Å3. The XRPD and IR results are mainly in accordance with the SEM-WDS results, having a higher level of correlativity. However, the analysis exposed a few discrepancies yielding several possible interpretations. The illustrated discrepancies were primarily caused by a slight unit-cell axial anisotropy i.e., thermal expansion. In this manner, the results yield a new geothermometric tool that is based on the unit-cell axial anisotropy. The investigated Sr-bearing celestines were formed during a Miocene intraplate volcanism, basaltic magmas, and associated brines lifted by the structural conduits (normal faults crosscutting the Sirt basin). The Sr-bearing fluids were then poured into and over the faulted and fractured lagoon-type gypsum, anhydrite Eocene sediments. The celestine minerals were produced within a ~ 368-430K (~ 95-157 oC) temperature range. The celestine is formed at slightly elevated temperature and pressure conditions, close to the shallow subsurface environment (over 250 bars).
PB  - Cambridge University Press
T2  - Mineralogical Magazine
T1  - Characterization, axial anisotropy and formation conditions of celestine from the Jabal Eghei (Nuqay) late Neogene – Pleistocene volcanic province, southern Libya: Constraints on the mineralogical geothermometer
VL  - 88
IS  - 1
SP  - 1
EP  - 18
DO  - 10.1180/mgm.2023.88
ER  - 

@article{
author = "Tančić, Pavle and Milošević, Maja and Spahić, Darko and Kostić, Bojan and Kremenović, Aleksandar and Poznanović-Spahić, Maja and Kovačević, Jovan",
year = "2024",
abstract = "Five celestine crystals are sampled from the (paleo)surface intervening between the late Miocene to Pleistocene basaltic sequences of the Jabal Eghei(Nuqay) volcanic province (southern Libya). The celestine specimens are characterized by applying the combination of the SEM-WDS, ICP/OES, XRPD, and IR methods. The celestine minerals are further analyzed for their color variations and minerogenetic framework. Three samples have greenish-blue-to-blue (480.4-482.5 nm), whereas the other two samples have blue-green color (cyan; 489.1-494.1 nm). The color purity ranges from 1.36-7.16. Their similarity of chemical content is fitting into the celestine near-end members, in which exclusively 1.6-4.1 at. % of Sr2+ content was substituted by Pb2+ (0.7-0.9 at. %), Ba2+ (0.5-0.7 at. %) and Ca2+ (0.2-0.8 at. %). The composition includes vacancies ranging from 1.0 to 1.9 at. % (observed only in three samples). The content of other chemical elements is minor. The resulting unit-cell parameters have the following ranges: a0=8.3578(9)-8.3705(6) Å; b0=5.3510(5)-5.3568(4) Å; c0=6.8683(7)-6.8767(2) Å and V0=307.17(5)-308.34(4) Å3. The XRPD and IR results are mainly in accordance with the SEM-WDS results, having a higher level of correlativity. However, the analysis exposed a few discrepancies yielding several possible interpretations. The illustrated discrepancies were primarily caused by a slight unit-cell axial anisotropy i.e., thermal expansion. In this manner, the results yield a new geothermometric tool that is based on the unit-cell axial anisotropy. The investigated Sr-bearing celestines were formed during a Miocene intraplate volcanism, basaltic magmas, and associated brines lifted by the structural conduits (normal faults crosscutting the Sirt basin). The Sr-bearing fluids were then poured into and over the faulted and fractured lagoon-type gypsum, anhydrite Eocene sediments. The celestine minerals were produced within a ~ 368-430K (~ 95-157 oC) temperature range. The celestine is formed at slightly elevated temperature and pressure conditions, close to the shallow subsurface environment (over 250 bars).",
publisher = "Cambridge University Press",
journal = "Mineralogical Magazine",
title = "Characterization, axial anisotropy and formation conditions of celestine from the Jabal Eghei (Nuqay) late Neogene – Pleistocene volcanic province, southern Libya: Constraints on the mineralogical geothermometer",
volume = "88",
number = "1",
pages = "1-18",
doi = "10.1180/mgm.2023.88"
}

Tančić, P., Milošević, M., Spahić, D., Kostić, B., Kremenović, A., Poznanović-Spahić, M.,& Kovačević, J.. (2024). Characterization, axial anisotropy and formation conditions of celestine from the Jabal Eghei (Nuqay) late Neogene – Pleistocene volcanic province, southern Libya: Constraints on the mineralogical geothermometer. in Mineralogical Magazine
Cambridge University Press., 88(1), 1-18.
https://doi.org/10.1180/mgm.2023.88

Tančić P, Milošević M, Spahić D, Kostić B, Kremenović A, Poznanović-Spahić M, Kovačević J. Characterization, axial anisotropy and formation conditions of celestine from the Jabal Eghei (Nuqay) late Neogene – Pleistocene volcanic province, southern Libya: Constraints on the mineralogical geothermometer. in Mineralogical Magazine. 2024;88(1):1-18.
doi:10.1180/mgm.2023.88 .

Tančić, Pavle, Milošević, Maja, Spahić, Darko, Kostić, Bojan, Kremenović, Aleksandar, Poznanović-Spahić, Maja, Kovačević, Jovan, "Characterization, axial anisotropy and formation conditions of celestine from the Jabal Eghei (Nuqay) late Neogene – Pleistocene volcanic province, southern Libya: Constraints on the mineralogical geothermometer" in Mineralogical Magazine, 88, no. 1 (2024):1-18,
https://doi.org/10.1180/mgm.2023.88 . .

TY  - JOUR
AU  - Tančić, Pavle
AU  - Milošević, Maja
AU  - Spahić, Darko
AU  - Kostić, Bojan
AU  - Kremenović, Aleksandar
AU  - Poznanović-Spahić, Maja
AU  - Kovačević, Jovan
PY  - 2024
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/7539
AB  - An error was introduced during production in the section of text on p. 10 under the heading “(v)
The option that various structural variations within the samples could take place”, in paragraph
six.
The published text reads:
“For possibility (b), the major celestines with the disregarded gypsum or anhydrite phases, the
results in Supplementary Tables S10 and S16 demonstrate that there is a slightly different ratio
between various crystallographic axes, such as c0 < a0 <b0 (samples 1 and 4), a0 < c0 <b0
(samples 2 and 3) and a0 = c0 < b0 (sample 5).”
The text ‘possibility (b)’ should be changed to ‘possibility 2’, and hence the descriptor ‘the major
celestines with the disregarded gypsum or anhydrite phases’ should be removed.
The correct text is:
“For possibility (2), the results in Supplementary Tables S10 and S16 demonstrate that there is a
slightly different ratio between various crystallographic axes, such as c0 < a0 <b0 (samples 1 and
4), a0 < c0 <b0 (samples 2 and 3) and a0 = c0 < b0 (sample 5).”
PB  - Cambridge University Press
T2  - Mineralogical Magazine
T1  - Characterisation, axial anisotropy, and formation conditions of celestine minerals from the Jabal Eghei (Nuqay) late Neogene – Pleistocene volcanic province, southeastern edge of the Sirt Basin, southern Libya: Constraints on the mineralogical geothermometer – ERRATUM
SP  - 1
EP  - 1
DO  - 10.1180/mgm.2024.12
ER  - 

@article{
author = "Tančić, Pavle and Milošević, Maja and Spahić, Darko and Kostić, Bojan and Kremenović, Aleksandar and Poznanović-Spahić, Maja and Kovačević, Jovan",
year = "2024",
abstract = "An error was introduced during production in the section of text on p. 10 under the heading “(v)
The option that various structural variations within the samples could take place”, in paragraph
six.
The published text reads:
“For possibility (b), the major celestines with the disregarded gypsum or anhydrite phases, the
results in Supplementary Tables S10 and S16 demonstrate that there is a slightly different ratio
between various crystallographic axes, such as c0 < a0 <b0 (samples 1 and 4), a0 < c0 <b0
(samples 2 and 3) and a0 = c0 < b0 (sample 5).”
The text ‘possibility (b)’ should be changed to ‘possibility 2’, and hence the descriptor ‘the major
celestines with the disregarded gypsum or anhydrite phases’ should be removed.
The correct text is:
“For possibility (2), the results in Supplementary Tables S10 and S16 demonstrate that there is a
slightly different ratio between various crystallographic axes, such as c0 < a0 <b0 (samples 1 and
4), a0 < c0 <b0 (samples 2 and 3) and a0 = c0 < b0 (sample 5).”",
publisher = "Cambridge University Press",
journal = "Mineralogical Magazine",
title = "Characterisation, axial anisotropy, and formation conditions of celestine minerals from the Jabal Eghei (Nuqay) late Neogene – Pleistocene volcanic province, southeastern edge of the Sirt Basin, southern Libya: Constraints on the mineralogical geothermometer – ERRATUM",
pages = "1-1",
doi = "10.1180/mgm.2024.12"
}

Tančić, P., Milošević, M., Spahić, D., Kostić, B., Kremenović, A., Poznanović-Spahić, M.,& Kovačević, J.. (2024). Characterisation, axial anisotropy, and formation conditions of celestine minerals from the Jabal Eghei (Nuqay) late Neogene – Pleistocene volcanic province, southeastern edge of the Sirt Basin, southern Libya: Constraints on the mineralogical geothermometer – ERRATUM. in Mineralogical Magazine
Cambridge University Press., 1-1.
https://doi.org/10.1180/mgm.2024.12

Tančić P, Milošević M, Spahić D, Kostić B, Kremenović A, Poznanović-Spahić M, Kovačević J. Characterisation, axial anisotropy, and formation conditions of celestine minerals from the Jabal Eghei (Nuqay) late Neogene – Pleistocene volcanic province, southeastern edge of the Sirt Basin, southern Libya: Constraints on the mineralogical geothermometer – ERRATUM. in Mineralogical Magazine. 2024;:1-1.
doi:10.1180/mgm.2024.12 .

Tančić, Pavle, Milošević, Maja, Spahić, Darko, Kostić, Bojan, Kremenović, Aleksandar, Poznanović-Spahić, Maja, Kovačević, Jovan, "Characterisation, axial anisotropy, and formation conditions of celestine minerals from the Jabal Eghei (Nuqay) late Neogene – Pleistocene volcanic province, southeastern edge of the Sirt Basin, southern Libya: Constraints on the mineralogical geothermometer – ERRATUM" in Mineralogical Magazine (2024):1-1,
https://doi.org/10.1180/mgm.2024.12 . .

TY  - JOUR
AU  - Tančić, Pavle
AU  - Milošević, Maja
AU  - Spahić, Darko
AU  - Kostić, Bojan
AU  - Kremenović, Aleksandar
AU  - Poznanović-Spahić, Maja
AU  - Kovačević, Jovan
PY  - 2024
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/7538
AB  - Five celestine crystals are sampled from the (paleo)surface intervening between the late Miocene to Pleistocene basaltic sequences of the Jabal Eghei(Nuqay) volcanic province (southern Libya). The celestine specimens are characterized by applying the combination of the SEM-WDS, ICP/OES, XRPD, and IR methods. The celestine minerals are further analyzed for their color variations and minerogenetic framework. Three samples have greenish-blue-to-blue (480.4-482.5 nm), whereas the other two samples have blue-green color (cyan; 489.1-494.1 nm). The color purity ranges from 1.36-7.16. Their similarity of chemical content is fitting into the celestine near-end members, in which exclusively 1.6-4.1 at. % of Sr2+ content was substituted by Pb2+ (0.7-0.9 at. %), Ba2+ (0.5-0.7 at. %) and Ca2+ (0.2-0.8 at. %). The composition includes vacancies ranging from 1.0 to 1.9 at. % (observed only in three samples). The content of other chemical elements is minor. The resulting unit-cell parameters have the following ranges: a0=8.3578(9)-8.3705(6) Å; b0=5.3510(5)-5.3568(4) Å; c0=6.8683(7)-6.8767(2) Å and V0=307.17(5)-308.34(4) Å3. The XRPD and IR results are mainly in accordance with the SEM-WDS results, having a higher level of correlativity. However, the analysis exposed a few discrepancies yielding several possible interpretations. The illustrated discrepancies were primarily caused by a slight unit-cell axial anisotropy i.e., thermal expansion. In this manner, the results yield a new geothermometric tool that is based on the unit-cell axial anisotropy. The investigated Sr-bearing celestines were formed during a Miocene intraplate volcanism, basaltic magmas, and associated brines lifted by the structural conduits (normal faults crosscutting the Sirt basin). The Sr-bearing fluids were then poured into and over the faulted and fractured lagoon-type gypsum, anhydrite Eocene sediments. The celestine minerals were produced within a ~ 368-430K (~ 95-157 oC) temperature range. The celestine is formed at slightly elevated temperature and pressure conditions, close to the shallow subsurface environment (over 250 bars).
PB  - Cambridge University Press
T2  - Mineralogical Magazine
T1  - Characterization, axial anisotropy and formation conditions of celestine from the Jabal Eghei (Nuqay) late Neogene – Pleistocene volcanic province, southern Libya: Constraints on the mineralogical geothermometer
VL  - 88
IS  - 1
SP  - 1
EP  - 18
DO  - 10.1180/mgm.2023.88
ER  - 

@article{
author = "Tančić, Pavle and Milošević, Maja and Spahić, Darko and Kostić, Bojan and Kremenović, Aleksandar and Poznanović-Spahić, Maja and Kovačević, Jovan",
year = "2024",
abstract = "Five celestine crystals are sampled from the (paleo)surface intervening between the late Miocene to Pleistocene basaltic sequences of the Jabal Eghei(Nuqay) volcanic province (southern Libya). The celestine specimens are characterized by applying the combination of the SEM-WDS, ICP/OES, XRPD, and IR methods. The celestine minerals are further analyzed for their color variations and minerogenetic framework. Three samples have greenish-blue-to-blue (480.4-482.5 nm), whereas the other two samples have blue-green color (cyan; 489.1-494.1 nm). The color purity ranges from 1.36-7.16. Their similarity of chemical content is fitting into the celestine near-end members, in which exclusively 1.6-4.1 at. % of Sr2+ content was substituted by Pb2+ (0.7-0.9 at. %), Ba2+ (0.5-0.7 at. %) and Ca2+ (0.2-0.8 at. %). The composition includes vacancies ranging from 1.0 to 1.9 at. % (observed only in three samples). The content of other chemical elements is minor. The resulting unit-cell parameters have the following ranges: a0=8.3578(9)-8.3705(6) Å; b0=5.3510(5)-5.3568(4) Å; c0=6.8683(7)-6.8767(2) Å and V0=307.17(5)-308.34(4) Å3. The XRPD and IR results are mainly in accordance with the SEM-WDS results, having a higher level of correlativity. However, the analysis exposed a few discrepancies yielding several possible interpretations. The illustrated discrepancies were primarily caused by a slight unit-cell axial anisotropy i.e., thermal expansion. In this manner, the results yield a new geothermometric tool that is based on the unit-cell axial anisotropy. The investigated Sr-bearing celestines were formed during a Miocene intraplate volcanism, basaltic magmas, and associated brines lifted by the structural conduits (normal faults crosscutting the Sirt basin). The Sr-bearing fluids were then poured into and over the faulted and fractured lagoon-type gypsum, anhydrite Eocene sediments. The celestine minerals were produced within a ~ 368-430K (~ 95-157 oC) temperature range. The celestine is formed at slightly elevated temperature and pressure conditions, close to the shallow subsurface environment (over 250 bars).",
publisher = "Cambridge University Press",
journal = "Mineralogical Magazine",
title = "Characterization, axial anisotropy and formation conditions of celestine from the Jabal Eghei (Nuqay) late Neogene – Pleistocene volcanic province, southern Libya: Constraints on the mineralogical geothermometer",
volume = "88",
number = "1",
pages = "1-18",
doi = "10.1180/mgm.2023.88"
}

Tančić, P., Milošević, M., Spahić, D., Kostić, B., Kremenović, A., Poznanović-Spahić, M.,& Kovačević, J.. (2024). Characterization, axial anisotropy and formation conditions of celestine from the Jabal Eghei (Nuqay) late Neogene – Pleistocene volcanic province, southern Libya: Constraints on the mineralogical geothermometer. in Mineralogical Magazine
Cambridge University Press., 88(1), 1-18.
https://doi.org/10.1180/mgm.2023.88

Tančić P, Milošević M, Spahić D, Kostić B, Kremenović A, Poznanović-Spahić M, Kovačević J. Characterization, axial anisotropy and formation conditions of celestine from the Jabal Eghei (Nuqay) late Neogene – Pleistocene volcanic province, southern Libya: Constraints on the mineralogical geothermometer. in Mineralogical Magazine. 2024;88(1):1-18.
doi:10.1180/mgm.2023.88 .

Tančić, Pavle, Milošević, Maja, Spahić, Darko, Kostić, Bojan, Kremenović, Aleksandar, Poznanović-Spahić, Maja, Kovačević, Jovan, "Characterization, axial anisotropy and formation conditions of celestine from the Jabal Eghei (Nuqay) late Neogene – Pleistocene volcanic province, southern Libya: Constraints on the mineralogical geothermometer" in Mineralogical Magazine, 88, no. 1 (2024):1-18,
https://doi.org/10.1180/mgm.2023.88 . .

TY  - JOUR
AU  - Lugonja, Nikoleta
AU  - Marinković, Vesna
AU  - Pucarević, Mira
AU  - Miletić, Srđan
AU  - Stojić, Nataša
AU  - Crnković, Dragan
AU  - Vrvić, Miroslav
PY  - 2024
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/7604
AB  - Human milk is a biofluid with a unique composition among mammalian milks. Besides this milk’s major components, its bioactive compounds, like hormones, immune factors, and oligosaccharides, are unique and important for infant growth and development. The best form of nutrition for term and preterm infants is the mother’s own milk. However, in the absence of the mother’s own milk, donor milk should be made available. Milk banks support neonatal intensive care units by providing preterm infants with human milk that generally has reasonable nutritive value for this sensitive population. However, neither mother’s own milk nor donor milk has sufficient energy content for the growth of preterm babies, so adequate human milk supplementation is crucial for their progress. Due to the different characteristics of human breast milk, as well as ubiquitous environmental pollutants, such as microplastics, new methods are required for monitoring the quality and characteristics of human milk, which will lay a solid foundation for the further development and progress of human milk research.
PB  - MDPI
T2  - Foods
T1  - Human Milk-The Biofluid That Nourishes Infants from the First Day of Life
VL  - 13
IS  - 9
SP  - 1298
DO  - 10.3390/foods13091298
ER  - 

@article{
author = "Lugonja, Nikoleta and Marinković, Vesna and Pucarević, Mira and Miletić, Srđan and Stojić, Nataša and Crnković, Dragan and Vrvić, Miroslav",
year = "2024",
abstract = "Human milk is a biofluid with a unique composition among mammalian milks. Besides this milk’s major components, its bioactive compounds, like hormones, immune factors, and oligosaccharides, are unique and important for infant growth and development. The best form of nutrition for term and preterm infants is the mother’s own milk. However, in the absence of the mother’s own milk, donor milk should be made available. Milk banks support neonatal intensive care units by providing preterm infants with human milk that generally has reasonable nutritive value for this sensitive population. However, neither mother’s own milk nor donor milk has sufficient energy content for the growth of preterm babies, so adequate human milk supplementation is crucial for their progress. Due to the different characteristics of human breast milk, as well as ubiquitous environmental pollutants, such as microplastics, new methods are required for monitoring the quality and characteristics of human milk, which will lay a solid foundation for the further development and progress of human milk research.",
publisher = "MDPI",
journal = "Foods",
title = "Human Milk-The Biofluid That Nourishes Infants from the First Day of Life",
volume = "13",
number = "9",
pages = "1298",
doi = "10.3390/foods13091298"
}

Lugonja, N., Marinković, V., Pucarević, M., Miletić, S., Stojić, N., Crnković, D.,& Vrvić, M.. (2024). Human Milk-The Biofluid That Nourishes Infants from the First Day of Life. in Foods
MDPI., 13(9), 1298.
https://doi.org/10.3390/foods13091298

Lugonja N, Marinković V, Pucarević M, Miletić S, Stojić N, Crnković D, Vrvić M. Human Milk-The Biofluid That Nourishes Infants from the First Day of Life. in Foods. 2024;13(9):1298.
doi:10.3390/foods13091298 .

Lugonja, Nikoleta, Marinković, Vesna, Pucarević, Mira, Miletić, Srđan, Stojić, Nataša, Crnković, Dragan, Vrvić, Miroslav, "Human Milk-The Biofluid That Nourishes Infants from the First Day of Life" in Foods, 13, no. 9 (2024):1298,
https://doi.org/10.3390/foods13091298 . .