Geochemical investigations of sedimentary rocks - fossil fuels and environmental pollutants

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Geochemical investigations of sedimentary rocks - fossil fuels and environmental pollutants (en)
Геохемијска испитивања седиментних стена - фосилна горива и загађивачи животне средине (sr)
Geohemijska ispitivanja sedimentnih stena - fosilna goriva i zagađivači životne sredine (sr_RS)
Authors

Publications

Geochromatographic migration of oil pollution from a heating plant to river sediments

Samelak, Ivan; Balaban, Milica; Antić, Mališa; Šolević-Knudsen, Tatjana; Jovančićević, Branimir

(Springer Heidelberg, Heidelberg, 2020)

TY  - JOUR
AU  - Samelak, Ivan
AU  - Balaban, Milica
AU  - Antić, Mališa
AU  - Šolević-Knudsen, Tatjana
AU  - Jovančićević, Branimir
PY  - 2020
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/5352
AB  - Many pollution sources are difficult to identify because pollutants are transported far away into complex environments. In particular, the mechanisms of petroleum migration in sediments are poorly known. Here, we studied two sediments from the circuit of a heating plant and three sediments located at 100, 200 and 300 m away from the plant. Saturated hydrocarbons were isolated and group composition was determined by column chromatography. n-Alkanes, terpanes and steranes were analyzed by gas chromatography-mass spectrometry. Results show that the amount of short n-alkanes increases during migration, which indicates the migration mechanism. Results on steranes reveal a geochromatographic migration of the oil, where the fastest eluting stereoisomers display the longest migration path. Changes in the distribution of biological markers are explained by migration in water.
PB  - Springer Heidelberg, Heidelberg
T2  - Environmental Chemistry Letters
T1  - Geochromatographic migration of oil pollution from a heating plant to river sediments
EP  - 466
IS  - 2
SP  - 459
VL  - 18
DO  - 10.1007/s10311-019-00937-2
ER  - 
@article{
author = "Samelak, Ivan and Balaban, Milica and Antić, Mališa and Šolević-Knudsen, Tatjana and Jovančićević, Branimir",
year = "2020",
abstract = "Many pollution sources are difficult to identify because pollutants are transported far away into complex environments. In particular, the mechanisms of petroleum migration in sediments are poorly known. Here, we studied two sediments from the circuit of a heating plant and three sediments located at 100, 200 and 300 m away from the plant. Saturated hydrocarbons were isolated and group composition was determined by column chromatography. n-Alkanes, terpanes and steranes were analyzed by gas chromatography-mass spectrometry. Results show that the amount of short n-alkanes increases during migration, which indicates the migration mechanism. Results on steranes reveal a geochromatographic migration of the oil, where the fastest eluting stereoisomers display the longest migration path. Changes in the distribution of biological markers are explained by migration in water.",
publisher = "Springer Heidelberg, Heidelberg",
journal = "Environmental Chemistry Letters",
title = "Geochromatographic migration of oil pollution from a heating plant to river sediments",
pages = "466-459",
number = "2",
volume = "18",
doi = "10.1007/s10311-019-00937-2"
}
Samelak, I., Balaban, M., Antić, M., Šolević-Knudsen, T.,& Jovančićević, B.. (2020). Geochromatographic migration of oil pollution from a heating plant to river sediments. in Environmental Chemistry Letters
Springer Heidelberg, Heidelberg., 18(2), 459-466.
https://doi.org/10.1007/s10311-019-00937-2
Samelak I, Balaban M, Antić M, Šolević-Knudsen T, Jovančićević B. Geochromatographic migration of oil pollution from a heating plant to river sediments. in Environmental Chemistry Letters. 2020;18(2):459-466.
doi:10.1007/s10311-019-00937-2 .
Samelak, Ivan, Balaban, Milica, Antić, Mališa, Šolević-Knudsen, Tatjana, Jovančićević, Branimir, "Geochromatographic migration of oil pollution from a heating plant to river sediments" in Environmental Chemistry Letters, 18, no. 2 (2020):459-466,
https://doi.org/10.1007/s10311-019-00937-2 . .
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Chemical Composition of the Essential Oils of Three Ocimum basilicum L. Cultivars from Serbia

Ilić, Aleksandra S.; Antić, Mališa; Jelačić, Slavica; Šolević-Knudsen, Tatjana

(Academic Press, 2019)

TY  - JOUR
AU  - Ilić, Aleksandra S.
AU  - Antić, Mališa
AU  - Jelačić, Slavica
AU  - Šolević-Knudsen, Tatjana
PY  - 2019
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/5160
AB  - Basil essential oil (BEO) contains a wide range of chemical compounds whose content may vary depending on chemotypes, environmental conditions, agronomic techniques and particularly the origin of the plant. In our present study, essential oils (EOs) were isolated by hydrodistillation method from dry herbs of three basil cultivars and analyzed by GC-FID and GC-MS. Two of the tested cultivars belong to sweet basil group (B-1 and B-2) while the third one was large leafed 'Genovese' basil (B-3). EO content in the dry herb was 0.65%, 0.41% and 0.62% respectively. The main classes of compounds of B1EO and B3EO were sesquiterpene hydrocarbons (38.39% and 37.95%), oxygenated monoterpenes (25.44% and 28.04%) and phenylpropanoids (17.43% and 15.71%). The main constituents of both EOs were monoterpene alcohol linalool (13.68% and 15.38%), phenoyl derivate eugenol (10.83% and 8.97%) and sesquiterpene hydrocarbon alpha-bergamotene (8.12% and 9.25%). In both EOs, epi-bicyclosesquiphellandrene was detected in considerable amount (7.03% and 8.07%). The most abundant compound classes in B2EO were oxygenated monoterpenes (52.07%), sesquiterpene hydrocarbons (24.27%) and phenylpropanoids (10.95%). Linalool was the dominant compound (40.97%), followed by epi-bicyclosesquiphellandrene (8.70%) and methyl chavicol (7.92%). The results showed complex chemical composition of BEOs and pointed out the presence of biologically active compounds of importance for different branches of the pharmaceutical, chemical and food industry. Although there are differences in the chemical composition of the BEOs, the obtained results show that all of the tested cultivars are rich in compounds which are responsible for biological activities.
PB  - Academic Press
T2  - Notulae Botanicae Horti Agrobotanici Cluj-Napoca
T1  - Chemical Composition of the Essential Oils of Three Ocimum basilicum L. Cultivars from Serbia
EP  - 351
IS  - 2
SP  - 347
VL  - 47
DO  - 10.15835/nbha47111250
ER  - 
@article{
author = "Ilić, Aleksandra S. and Antić, Mališa and Jelačić, Slavica and Šolević-Knudsen, Tatjana",
year = "2019",
abstract = "Basil essential oil (BEO) contains a wide range of chemical compounds whose content may vary depending on chemotypes, environmental conditions, agronomic techniques and particularly the origin of the plant. In our present study, essential oils (EOs) were isolated by hydrodistillation method from dry herbs of three basil cultivars and analyzed by GC-FID and GC-MS. Two of the tested cultivars belong to sweet basil group (B-1 and B-2) while the third one was large leafed 'Genovese' basil (B-3). EO content in the dry herb was 0.65%, 0.41% and 0.62% respectively. The main classes of compounds of B1EO and B3EO were sesquiterpene hydrocarbons (38.39% and 37.95%), oxygenated monoterpenes (25.44% and 28.04%) and phenylpropanoids (17.43% and 15.71%). The main constituents of both EOs were monoterpene alcohol linalool (13.68% and 15.38%), phenoyl derivate eugenol (10.83% and 8.97%) and sesquiterpene hydrocarbon alpha-bergamotene (8.12% and 9.25%). In both EOs, epi-bicyclosesquiphellandrene was detected in considerable amount (7.03% and 8.07%). The most abundant compound classes in B2EO were oxygenated monoterpenes (52.07%), sesquiterpene hydrocarbons (24.27%) and phenylpropanoids (10.95%). Linalool was the dominant compound (40.97%), followed by epi-bicyclosesquiphellandrene (8.70%) and methyl chavicol (7.92%). The results showed complex chemical composition of BEOs and pointed out the presence of biologically active compounds of importance for different branches of the pharmaceutical, chemical and food industry. Although there are differences in the chemical composition of the BEOs, the obtained results show that all of the tested cultivars are rich in compounds which are responsible for biological activities.",
publisher = "Academic Press",
journal = "Notulae Botanicae Horti Agrobotanici Cluj-Napoca",
title = "Chemical Composition of the Essential Oils of Three Ocimum basilicum L. Cultivars from Serbia",
pages = "351-347",
number = "2",
volume = "47",
doi = "10.15835/nbha47111250"
}
Ilić, A. S., Antić, M., Jelačić, S.,& Šolević-Knudsen, T.. (2019). Chemical Composition of the Essential Oils of Three Ocimum basilicum L. Cultivars from Serbia. in Notulae Botanicae Horti Agrobotanici Cluj-Napoca
Academic Press., 47(2), 347-351.
https://doi.org/10.15835/nbha47111250
Ilić AS, Antić M, Jelačić S, Šolević-Knudsen T. Chemical Composition of the Essential Oils of Three Ocimum basilicum L. Cultivars from Serbia. in Notulae Botanicae Horti Agrobotanici Cluj-Napoca. 2019;47(2):347-351.
doi:10.15835/nbha47111250 .
Ilić, Aleksandra S., Antić, Mališa, Jelačić, Slavica, Šolević-Knudsen, Tatjana, "Chemical Composition of the Essential Oils of Three Ocimum basilicum L. Cultivars from Serbia" in Notulae Botanicae Horti Agrobotanici Cluj-Napoca, 47, no. 2 (2019):347-351,
https://doi.org/10.15835/nbha47111250 . .
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Application of alkane biological markers in the assessment of the origin of oil pollutants in the soil and recent river sediments (River Vrbas, Bosnia and Herzegovina)

Samelak, Ivan; Balaban, Milica; Vidović, Nada; Koljancić, Nemanja; Antić, Mališa; Šolević-Knudsen, Tatjana; Jovančićević, Branimir

(Srpsko hemijsko društvo, Beograd, 2018)

TY  - JOUR
AU  - Samelak, Ivan
AU  - Balaban, Milica
AU  - Vidović, Nada
AU  - Koljancić, Nemanja
AU  - Antić, Mališa
AU  - Šolević-Knudsen, Tatjana
AU  - Jovančićević, Branimir
PY  - 2018
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/4760
AB  - In this paper, an attempt was made to contribute to the use of biological markers, n-alkanes, and polycyclic alkanes of the sterane and terpane type, in the assessment of the source of oil pollutants in the environment using the example of the correlation between recent river and coastal sediments,. Four samples of recent river sediments of the Vrbas River and four samples of adjacent bank sediments (soils), in the part of the River that belongs to the city of Banja Luka (Bosnia and Herzegovina) were analyzed. In the alkane fractions of isolated extracts, a bimodal distribution of the n-alkanes was observed. Lower homologues dominated in the recent river sediments with maximum at C15, but higher n-alkanes dominated in the soil samples, with a maximum at n-C29 or at n-C31. The higher concentration of steranes and terpanes with oil type distributions in the recent/fresh river sediments (compared to the bank sediments) represents evidence that lower n-alkanes originate from oil sources. The higher content of total hydrocarbons in the recent river sediments than in the bank sediments further confirms this conclusion. At the same time, these fundamental considerations provide evidence that oil pollution primarily occurred in the water flow and then the oil pollutants propagated towards the riverbank.
PB  - Srpsko hemijsko društvo, Beograd
T2  - JOURNAL OF THE SERBIAN CHEMICAL SOCIETY
T1  - Application of alkane biological markers in the assessment of the origin of oil pollutants in the soil and recent river sediments (River Vrbas, Bosnia and Herzegovina)
EP  - 1175
IS  - 10
SP  - 1167
VL  - 83
DO  - 10.2298/JSC180501061S
ER  - 
@article{
author = "Samelak, Ivan and Balaban, Milica and Vidović, Nada and Koljancić, Nemanja and Antić, Mališa and Šolević-Knudsen, Tatjana and Jovančićević, Branimir",
year = "2018",
abstract = "In this paper, an attempt was made to contribute to the use of biological markers, n-alkanes, and polycyclic alkanes of the sterane and terpane type, in the assessment of the source of oil pollutants in the environment using the example of the correlation between recent river and coastal sediments,. Four samples of recent river sediments of the Vrbas River and four samples of adjacent bank sediments (soils), in the part of the River that belongs to the city of Banja Luka (Bosnia and Herzegovina) were analyzed. In the alkane fractions of isolated extracts, a bimodal distribution of the n-alkanes was observed. Lower homologues dominated in the recent river sediments with maximum at C15, but higher n-alkanes dominated in the soil samples, with a maximum at n-C29 or at n-C31. The higher concentration of steranes and terpanes with oil type distributions in the recent/fresh river sediments (compared to the bank sediments) represents evidence that lower n-alkanes originate from oil sources. The higher content of total hydrocarbons in the recent river sediments than in the bank sediments further confirms this conclusion. At the same time, these fundamental considerations provide evidence that oil pollution primarily occurred in the water flow and then the oil pollutants propagated towards the riverbank.",
publisher = "Srpsko hemijsko društvo, Beograd",
journal = "JOURNAL OF THE SERBIAN CHEMICAL SOCIETY",
title = "Application of alkane biological markers in the assessment of the origin of oil pollutants in the soil and recent river sediments (River Vrbas, Bosnia and Herzegovina)",
pages = "1175-1167",
number = "10",
volume = "83",
doi = "10.2298/JSC180501061S"
}
Samelak, I., Balaban, M., Vidović, N., Koljancić, N., Antić, M., Šolević-Knudsen, T.,& Jovančićević, B.. (2018). Application of alkane biological markers in the assessment of the origin of oil pollutants in the soil and recent river sediments (River Vrbas, Bosnia and Herzegovina). in JOURNAL OF THE SERBIAN CHEMICAL SOCIETY
Srpsko hemijsko društvo, Beograd., 83(10), 1167-1175.
https://doi.org/10.2298/JSC180501061S
Samelak I, Balaban M, Vidović N, Koljancić N, Antić M, Šolević-Knudsen T, Jovančićević B. Application of alkane biological markers in the assessment of the origin of oil pollutants in the soil and recent river sediments (River Vrbas, Bosnia and Herzegovina). in JOURNAL OF THE SERBIAN CHEMICAL SOCIETY. 2018;83(10):1167-1175.
doi:10.2298/JSC180501061S .
Samelak, Ivan, Balaban, Milica, Vidović, Nada, Koljancić, Nemanja, Antić, Mališa, Šolević-Knudsen, Tatjana, Jovančićević, Branimir, "Application of alkane biological markers in the assessment of the origin of oil pollutants in the soil and recent river sediments (River Vrbas, Bosnia and Herzegovina)" in JOURNAL OF THE SERBIAN CHEMICAL SOCIETY, 83, no. 10 (2018):1167-1175,
https://doi.org/10.2298/JSC180501061S . .
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Ultrasound and shacking-assisted water-leaching of anions and cations from fly ash

Savić-Bisercić, Marjetka; Pezo, Lato; Sredović-Ignjatović, Ivana; Ignjatović, Ljubiša M.; Savić, Andrija; Jovanović, Uroš D.; Andrić, Velibor

(Srpsko hemijsko društvo, Beograd, 2016)

TY  - JOUR
AU  - Savić-Bisercić, Marjetka
AU  - Pezo, Lato
AU  - Sredović-Ignjatović, Ivana
AU  - Ignjatović, Ljubiša M.
AU  - Savić, Andrija
AU  - Jovanović, Uroš D.
AU  - Andrić, Velibor
PY  - 2016
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/4030
AB  - Two mechanical extraction techniques were used for the extraction of environmentaly interesting components of coal fly ash: shaking, during which the extraction process lasted from 6 up to 24 h, and sonication that lasted from 15 up to 60 min, using water as extractant. The concentration of anions in fly ash extracts was determined by ion chromatography, while atomic absorption spectrometry was used for determination of: As, Pb, Cd, Ni, Cr, Zn, Cu, Fe, Mn and Al. The ultrasonication yielded slightly higher amounts of extracted anions as well as Pb, Al, Mn and Fe cations, while shaking-assisted extraction was more efficient for the Cr, As, Zn and Ni ions. The changes in pH value, particle size distribution within colloid solution, zeta potential and conductivity during ultrasound-assisted extraction were measured in order to explain changes that occur on the surface of fly ash particles contacting water and different processes (adsorption, ion exchange and flocculation) that develop under natural conditions. Principal Component Analysis was used for assessing the effect of observed process parameters. It is essential to evaluate quantity of these elements leachable from coal fly ash into the surface waters in natural conditions in order to prevent contamination of the environment.
PB  - Srpsko hemijsko društvo, Beograd
T2  - JOURNAL OF THE SERBIAN CHEMICAL SOCIETY
T1  - Ultrasound and shacking-assisted water-leaching of anions and cations from fly ash
EP  - 827
IS  - 7
SP  - 813
VL  - 81
DO  - 10.2298/JSC151222027B
ER  - 
@article{
author = "Savić-Bisercić, Marjetka and Pezo, Lato and Sredović-Ignjatović, Ivana and Ignjatović, Ljubiša M. and Savić, Andrija and Jovanović, Uroš D. and Andrić, Velibor",
year = "2016",
abstract = "Two mechanical extraction techniques were used for the extraction of environmentaly interesting components of coal fly ash: shaking, during which the extraction process lasted from 6 up to 24 h, and sonication that lasted from 15 up to 60 min, using water as extractant. The concentration of anions in fly ash extracts was determined by ion chromatography, while atomic absorption spectrometry was used for determination of: As, Pb, Cd, Ni, Cr, Zn, Cu, Fe, Mn and Al. The ultrasonication yielded slightly higher amounts of extracted anions as well as Pb, Al, Mn and Fe cations, while shaking-assisted extraction was more efficient for the Cr, As, Zn and Ni ions. The changes in pH value, particle size distribution within colloid solution, zeta potential and conductivity during ultrasound-assisted extraction were measured in order to explain changes that occur on the surface of fly ash particles contacting water and different processes (adsorption, ion exchange and flocculation) that develop under natural conditions. Principal Component Analysis was used for assessing the effect of observed process parameters. It is essential to evaluate quantity of these elements leachable from coal fly ash into the surface waters in natural conditions in order to prevent contamination of the environment.",
publisher = "Srpsko hemijsko društvo, Beograd",
journal = "JOURNAL OF THE SERBIAN CHEMICAL SOCIETY",
title = "Ultrasound and shacking-assisted water-leaching of anions and cations from fly ash",
pages = "827-813",
number = "7",
volume = "81",
doi = "10.2298/JSC151222027B"
}
Savić-Bisercić, M., Pezo, L., Sredović-Ignjatović, I., Ignjatović, L. M., Savić, A., Jovanović, U. D.,& Andrić, V.. (2016). Ultrasound and shacking-assisted water-leaching of anions and cations from fly ash. in JOURNAL OF THE SERBIAN CHEMICAL SOCIETY
Srpsko hemijsko društvo, Beograd., 81(7), 813-827.
https://doi.org/10.2298/JSC151222027B
Savić-Bisercić M, Pezo L, Sredović-Ignjatović I, Ignjatović LM, Savić A, Jovanović UD, Andrić V. Ultrasound and shacking-assisted water-leaching of anions and cations from fly ash. in JOURNAL OF THE SERBIAN CHEMICAL SOCIETY. 2016;81(7):813-827.
doi:10.2298/JSC151222027B .
Savić-Bisercić, Marjetka, Pezo, Lato, Sredović-Ignjatović, Ivana, Ignjatović, Ljubiša M., Savić, Andrija, Jovanović, Uroš D., Andrić, Velibor, "Ultrasound and shacking-assisted water-leaching of anions and cations from fly ash" in JOURNAL OF THE SERBIAN CHEMICAL SOCIETY, 81, no. 7 (2016):813-827,
https://doi.org/10.2298/JSC151222027B . .
6
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7

Aqueous extraction of anions from coal and fly ash followed by ion-chromatographic determination

Tasić, Aleksandra M.; Sredović-Ignjatović, Ivana; Ignjatović, Ljubiša M.; Duranović, Danijel; Antić, Mališa

(Srpsko hemijsko društvo, Beograd, 2016)

TY  - JOUR
AU  - Tasić, Aleksandra M.
AU  - Sredović-Ignjatović, Ivana
AU  - Ignjatović, Ljubiša M.
AU  - Duranović, Danijel
AU  - Antić, Mališa
PY  - 2016
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/4046
AB  - Three different techniques were applied for the aqueous extraction of anions from coal and fly ash: rotary mixer-and ultrasonic-assisted extraction with different duration time, and microwave-assisted extraction at different temperatures. Validation showed that the ion-chromatographic method was suitable for the analysis of anions in coal and fly ash extracts. The variations in the amounts of anions using different extraction times during rotary-assisted extraction were minimal for all investigated anions. The efficiency of ultrasound-assisted extraction of anions from coal depended on the sonication time and was highest at 30 min. The ultrasound-assisted extraction was less efficient for the extraction of anions from fly ash than rotary-assisted extraction. Increase of temperature in the microwave-assisted extraction had a positive effect on the amounts of all anions extracted from coal and sulphate from fly ash, while the amounts of fluoride and chloride in fly ash extracts decreased. The microwave-assisted extraction of coal at 150 degrees C was compared with standard ASTM methods, and results were in good agreement only for chloride. Changes in the pH value and conductivity during ultrasound-assisted extraction were measured in order to explain changes on the surface of coal particles in contact with water and different processes that occur under environmental conditions.
PB  - Srpsko hemijsko društvo, Beograd
T2  - JOURNAL OF THE SERBIAN CHEMICAL SOCIETY
T1  - Aqueous extraction of anions from coal and fly ash followed by ion-chromatographic determination
EP  - 1453
IS  - 12
SP  - 1441
VL  - 81
DO  - 10.2298/JSC160223086T
ER  - 
@article{
author = "Tasić, Aleksandra M. and Sredović-Ignjatović, Ivana and Ignjatović, Ljubiša M. and Duranović, Danijel and Antić, Mališa",
year = "2016",
abstract = "Three different techniques were applied for the aqueous extraction of anions from coal and fly ash: rotary mixer-and ultrasonic-assisted extraction with different duration time, and microwave-assisted extraction at different temperatures. Validation showed that the ion-chromatographic method was suitable for the analysis of anions in coal and fly ash extracts. The variations in the amounts of anions using different extraction times during rotary-assisted extraction were minimal for all investigated anions. The efficiency of ultrasound-assisted extraction of anions from coal depended on the sonication time and was highest at 30 min. The ultrasound-assisted extraction was less efficient for the extraction of anions from fly ash than rotary-assisted extraction. Increase of temperature in the microwave-assisted extraction had a positive effect on the amounts of all anions extracted from coal and sulphate from fly ash, while the amounts of fluoride and chloride in fly ash extracts decreased. The microwave-assisted extraction of coal at 150 degrees C was compared with standard ASTM methods, and results were in good agreement only for chloride. Changes in the pH value and conductivity during ultrasound-assisted extraction were measured in order to explain changes on the surface of coal particles in contact with water and different processes that occur under environmental conditions.",
publisher = "Srpsko hemijsko društvo, Beograd",
journal = "JOURNAL OF THE SERBIAN CHEMICAL SOCIETY",
title = "Aqueous extraction of anions from coal and fly ash followed by ion-chromatographic determination",
pages = "1453-1441",
number = "12",
volume = "81",
doi = "10.2298/JSC160223086T"
}
Tasić, A. M., Sredović-Ignjatović, I., Ignjatović, L. M., Duranović, D.,& Antić, M.. (2016). Aqueous extraction of anions from coal and fly ash followed by ion-chromatographic determination. in JOURNAL OF THE SERBIAN CHEMICAL SOCIETY
Srpsko hemijsko društvo, Beograd., 81(12), 1441-1453.
https://doi.org/10.2298/JSC160223086T
Tasić AM, Sredović-Ignjatović I, Ignjatović LM, Duranović D, Antić M. Aqueous extraction of anions from coal and fly ash followed by ion-chromatographic determination. in JOURNAL OF THE SERBIAN CHEMICAL SOCIETY. 2016;81(12):1441-1453.
doi:10.2298/JSC160223086T .
Tasić, Aleksandra M., Sredović-Ignjatović, Ivana, Ignjatović, Ljubiša M., Duranović, Danijel, Antić, Mališa, "Aqueous extraction of anions from coal and fly ash followed by ion-chromatographic determination" in JOURNAL OF THE SERBIAN CHEMICAL SOCIETY, 81, no. 12 (2016):1441-1453,
https://doi.org/10.2298/JSC160223086T . .

Comparison of sequential and single extraction in order to estimate the environmental impact of metals from fly ash

Tasić, Aleksandra M.; Sredović-Ignjatović, Ivana; Ignjatović, Ljubiša M.; Ilić, Marija A.; Antić, Mališa

(Srpsko hemijsko društvo, Beograd, 2016)

TY  - JOUR
AU  - Tasić, Aleksandra M.
AU  - Sredović-Ignjatović, Ivana
AU  - Ignjatović, Ljubiša M.
AU  - Ilić, Marija A.
AU  - Antić, Mališa
PY  - 2016
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/4047
AB  - The aim of this paper is to simulate leaching of metals from fly ash in different environmental conditions using ultrasound and microwave-assisted extraction techniques. Single-agent extraction and sequential extraction procedures were used to determine the levels of different metals leaching. The concentration of metals (Al, Fe, Mn, Cd, Co, Cr, Ni, Pb, Cu, As and Be) in fly ash extracts were measured by inductively coupled plasma-atomic emission spectrometry. Single-agent extractions of metals were conducted at sonication times of 10, 20, 30, 40 and 50 min. Single-agent extraction with deionized water was also performed by exposing samples to microwave radiation at temperature of 50 degrees C. The sequential extraction was conducted according to the BCR procedure which was modified and applied to study the partitioning of metals in coal fly ash. The microwave-assisted sequential extraction was performed at different extraction temperatures: 50, 100 and 150 degrees C. The partitioning of metals between the individual fractions was investigated and discussed. The efficiency of the extraction process for each step was examined. In addition, the results of the microwave-assisted sequential extraction are compared to the results obtained by standard ASTM method. The mobility of most elements contained in the fly ash is markedly pH sensitive.
PB  - Srpsko hemijsko društvo, Beograd
T2  - JOURNAL OF THE SERBIAN CHEMICAL SOCIETY
T1  - Comparison of sequential and single extraction in order to estimate the environmental impact of metals from fly ash
EP  - 1096
IS  - 9
SP  - 1081
VL  - 81
DO  - 10.2298/JSC160307038T
ER  - 
@article{
author = "Tasić, Aleksandra M. and Sredović-Ignjatović, Ivana and Ignjatović, Ljubiša M. and Ilić, Marija A. and Antić, Mališa",
year = "2016",
abstract = "The aim of this paper is to simulate leaching of metals from fly ash in different environmental conditions using ultrasound and microwave-assisted extraction techniques. Single-agent extraction and sequential extraction procedures were used to determine the levels of different metals leaching. The concentration of metals (Al, Fe, Mn, Cd, Co, Cr, Ni, Pb, Cu, As and Be) in fly ash extracts were measured by inductively coupled plasma-atomic emission spectrometry. Single-agent extractions of metals were conducted at sonication times of 10, 20, 30, 40 and 50 min. Single-agent extraction with deionized water was also performed by exposing samples to microwave radiation at temperature of 50 degrees C. The sequential extraction was conducted according to the BCR procedure which was modified and applied to study the partitioning of metals in coal fly ash. The microwave-assisted sequential extraction was performed at different extraction temperatures: 50, 100 and 150 degrees C. The partitioning of metals between the individual fractions was investigated and discussed. The efficiency of the extraction process for each step was examined. In addition, the results of the microwave-assisted sequential extraction are compared to the results obtained by standard ASTM method. The mobility of most elements contained in the fly ash is markedly pH sensitive.",
publisher = "Srpsko hemijsko društvo, Beograd",
journal = "JOURNAL OF THE SERBIAN CHEMICAL SOCIETY",
title = "Comparison of sequential and single extraction in order to estimate the environmental impact of metals from fly ash",
pages = "1096-1081",
number = "9",
volume = "81",
doi = "10.2298/JSC160307038T"
}
Tasić, A. M., Sredović-Ignjatović, I., Ignjatović, L. M., Ilić, M. A.,& Antić, M.. (2016). Comparison of sequential and single extraction in order to estimate the environmental impact of metals from fly ash. in JOURNAL OF THE SERBIAN CHEMICAL SOCIETY
Srpsko hemijsko društvo, Beograd., 81(9), 1081-1096.
https://doi.org/10.2298/JSC160307038T
Tasić AM, Sredović-Ignjatović I, Ignjatović LM, Ilić MA, Antić M. Comparison of sequential and single extraction in order to estimate the environmental impact of metals from fly ash. in JOURNAL OF THE SERBIAN CHEMICAL SOCIETY. 2016;81(9):1081-1096.
doi:10.2298/JSC160307038T .
Tasić, Aleksandra M., Sredović-Ignjatović, Ivana, Ignjatović, Ljubiša M., Ilić, Marija A., Antić, Mališa, "Comparison of sequential and single extraction in order to estimate the environmental impact of metals from fly ash" in JOURNAL OF THE SERBIAN CHEMICAL SOCIETY, 81, no. 9 (2016):1081-1096,
https://doi.org/10.2298/JSC160307038T . .
9
4
10

Degradability of n-alkanes during ex situ natural bioremediation of soil contaminated by heavy residual fuel oil (mazut)

Ramadan, Ali Mohamed Muftah; Knudsen-Šolević, Tatjana; Antić, Mališa; Beskoski, Vladimir; Vrvić, Miroslav M.; Schwarzbauer, Jan; Jovančićević, Branimir

(Srpsko hemijsko društvo, Beograd, 2013)

TY  - JOUR
AU  - Ramadan, Ali Mohamed Muftah
AU  - Knudsen-Šolević, Tatjana
AU  - Antić, Mališa
AU  - Beskoski, Vladimir
AU  - Vrvić, Miroslav M.
AU  - Schwarzbauer, Jan
AU  - Jovančićević, Branimir
PY  - 2013
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/3329
AB  - It is well known that during biodegradation of oil under natural geological conditions, or oil pollutants in the environment, degradation of hydrocarbons occurs according to a well-defined sequence. For example, the major changes during the degradation process of n-alkanes occur in the second, slight and third, moderate level (on the biodegradation scale from 1 to 10). According to previous research, in the fourth, heavy level, when intensive changes of phenanthrene and its methyl isomers begin, n-alkanes have already been completely removed. In this paper, the ex situ natural bioremediation (non-stimulated bioremediation, without addition of biomass, nutrient substances and biosurfactant) of soil contaminated with heavy residual fuel oil (mazut) was conducted during a period of 6 months. Low abundance of n-alkanes in the fraction of total saturated hydrocarbons in the initial sample (identification was possible only after concentration by the urea adduction technique) showed that the investigated oil pollutant was at the boundary between the third and the fourth biodegradation level. During the experiment, an intense degradation of phenanthrene and its methyl-, dimethyl- and trimethyl-isomers was not accompanied by the removal of the remaining n-alkanes. The abundance of n-alkanes remained at the initial low level, even at end of the experiment when the pollutant reached one of the highest biodegradation levels. These results showed that the non-stimulated biodegradation of some hydrocarbons, despite their high biodegradability, had not proceeded completely to the end, even at final degradation stages. Under the condition of reduced availability of some hydrocarbons, microorganisms tend to opt for the less biodegradable but more accessible hydrocarbons.
AB  - Dobro je poznato da se u toku biodegradacije nafte u prirodnim geološkim uslovima, ili naftnog zagađivača u životnoj sredini, degradacija ugljovodonika odigrava prema definisanom rasporedu. Na primer, glavne promene u procesu razgradnje normalnih alkana dešavaju se u toku drugog, "blagog", i trećeg, "umerenog", stupnja (na skali biodegradacije od 1 do 10). Prema dosadašnjim istraživanjima, u četvrtom stupnju, kada počinju intenzivne promene fenantrena i njegovih metil izomera, normalni alkani su već u potpunosti uklonjeni. U ovom radu u toku perioda od 6 meseci izvođena je ex situ prirodna bioremedijacija (nestimulisana bioremedijacija bez dodatka biomase, hranljivih sastojaka i biosurfaktanata) zemljišta zagađenog mazutom. Niska obilnost normalnih alkana u frakciji ukupnih zasićenih alkana u početnom uzorku (identifikacija je bila mogućna tek nakon koncentrovanja pomoću karbamida) pokazala je da je ispitivani naftni zagađivač na granici između trećeg i četvrtog stupnja biodegradacije. Tokom eksperimenta, intenzivnu razgradnju fenantrena i njegovih metil, dimetil i trimetil izomera nije pratilo uklanjanje ostatka normalnih alkana. Njihova obilnost je ostala na početnom, niskom nivou i na kraju eksperimenta kada je zagađivač dostigao jedan od najviših stepena biodegradacije. Dobijeni rezultati su pokazali da se razgradnja pojedinih ugljovodonika uprkos njihovoj visokoj biodegradabilnosti ne odigrava do potpunog kraja ni u završnim fazama degradacije. U uslovima njihove smanjene dostupnosti, mikroorganizmi se opredeljuju za teže degradabilne, ali dostupnije ugljovodonike.
PB  - Srpsko hemijsko društvo, Beograd
T2  - JOURNAL OF THE SERBIAN CHEMICAL SOCIETY
T1  - Degradability of n-alkanes during ex situ natural bioremediation of soil contaminated by heavy residual fuel oil (mazut)
T1  - Degradabilnost normalnih alkana za vreme ex situ prirodne bioremedijacije zemljišta zagađenog mazutom
EP  - 1043
IS  - 7
SP  - 1035
VL  - 78
DO  - 10.2298/JSC120829106A
ER  - 
@article{
author = "Ramadan, Ali Mohamed Muftah and Knudsen-Šolević, Tatjana and Antić, Mališa and Beskoski, Vladimir and Vrvić, Miroslav M. and Schwarzbauer, Jan and Jovančićević, Branimir",
year = "2013",
abstract = "It is well known that during biodegradation of oil under natural geological conditions, or oil pollutants in the environment, degradation of hydrocarbons occurs according to a well-defined sequence. For example, the major changes during the degradation process of n-alkanes occur in the second, slight and third, moderate level (on the biodegradation scale from 1 to 10). According to previous research, in the fourth, heavy level, when intensive changes of phenanthrene and its methyl isomers begin, n-alkanes have already been completely removed. In this paper, the ex situ natural bioremediation (non-stimulated bioremediation, without addition of biomass, nutrient substances and biosurfactant) of soil contaminated with heavy residual fuel oil (mazut) was conducted during a period of 6 months. Low abundance of n-alkanes in the fraction of total saturated hydrocarbons in the initial sample (identification was possible only after concentration by the urea adduction technique) showed that the investigated oil pollutant was at the boundary between the third and the fourth biodegradation level. During the experiment, an intense degradation of phenanthrene and its methyl-, dimethyl- and trimethyl-isomers was not accompanied by the removal of the remaining n-alkanes. The abundance of n-alkanes remained at the initial low level, even at end of the experiment when the pollutant reached one of the highest biodegradation levels. These results showed that the non-stimulated biodegradation of some hydrocarbons, despite their high biodegradability, had not proceeded completely to the end, even at final degradation stages. Under the condition of reduced availability of some hydrocarbons, microorganisms tend to opt for the less biodegradable but more accessible hydrocarbons., Dobro je poznato da se u toku biodegradacije nafte u prirodnim geološkim uslovima, ili naftnog zagađivača u životnoj sredini, degradacija ugljovodonika odigrava prema definisanom rasporedu. Na primer, glavne promene u procesu razgradnje normalnih alkana dešavaju se u toku drugog, "blagog", i trećeg, "umerenog", stupnja (na skali biodegradacije od 1 do 10). Prema dosadašnjim istraživanjima, u četvrtom stupnju, kada počinju intenzivne promene fenantrena i njegovih metil izomera, normalni alkani su već u potpunosti uklonjeni. U ovom radu u toku perioda od 6 meseci izvođena je ex situ prirodna bioremedijacija (nestimulisana bioremedijacija bez dodatka biomase, hranljivih sastojaka i biosurfaktanata) zemljišta zagađenog mazutom. Niska obilnost normalnih alkana u frakciji ukupnih zasićenih alkana u početnom uzorku (identifikacija je bila mogućna tek nakon koncentrovanja pomoću karbamida) pokazala je da je ispitivani naftni zagađivač na granici između trećeg i četvrtog stupnja biodegradacije. Tokom eksperimenta, intenzivnu razgradnju fenantrena i njegovih metil, dimetil i trimetil izomera nije pratilo uklanjanje ostatka normalnih alkana. Njihova obilnost je ostala na početnom, niskom nivou i na kraju eksperimenta kada je zagađivač dostigao jedan od najviših stepena biodegradacije. Dobijeni rezultati su pokazali da se razgradnja pojedinih ugljovodonika uprkos njihovoj visokoj biodegradabilnosti ne odigrava do potpunog kraja ni u završnim fazama degradacije. U uslovima njihove smanjene dostupnosti, mikroorganizmi se opredeljuju za teže degradabilne, ali dostupnije ugljovodonike.",
publisher = "Srpsko hemijsko društvo, Beograd",
journal = "JOURNAL OF THE SERBIAN CHEMICAL SOCIETY",
title = "Degradability of n-alkanes during ex situ natural bioremediation of soil contaminated by heavy residual fuel oil (mazut), Degradabilnost normalnih alkana za vreme ex situ prirodne bioremedijacije zemljišta zagađenog mazutom",
pages = "1043-1035",
number = "7",
volume = "78",
doi = "10.2298/JSC120829106A"
}
Ramadan, A. M. M., Knudsen-Šolević, T., Antić, M., Beskoski, V., Vrvić, M. M., Schwarzbauer, J.,& Jovančićević, B.. (2013). Degradability of n-alkanes during ex situ natural bioremediation of soil contaminated by heavy residual fuel oil (mazut). in JOURNAL OF THE SERBIAN CHEMICAL SOCIETY
Srpsko hemijsko društvo, Beograd., 78(7), 1035-1043.
https://doi.org/10.2298/JSC120829106A
Ramadan AMM, Knudsen-Šolević T, Antić M, Beskoski V, Vrvić MM, Schwarzbauer J, Jovančićević B. Degradability of n-alkanes during ex situ natural bioremediation of soil contaminated by heavy residual fuel oil (mazut). in JOURNAL OF THE SERBIAN CHEMICAL SOCIETY. 2013;78(7):1035-1043.
doi:10.2298/JSC120829106A .
Ramadan, Ali Mohamed Muftah, Knudsen-Šolević, Tatjana, Antić, Mališa, Beskoski, Vladimir, Vrvić, Miroslav M., Schwarzbauer, Jan, Jovančićević, Branimir, "Degradability of n-alkanes during ex situ natural bioremediation of soil contaminated by heavy residual fuel oil (mazut)" in JOURNAL OF THE SERBIAN CHEMICAL SOCIETY, 78, no. 7 (2013):1035-1043,
https://doi.org/10.2298/JSC120829106A . .
3
5
6

Quantitative determination of poly(vinylpyrrolidone) by 'On-line' pyrolysis coupled with gas chromatography

Antić, Vesna; Antić, Mališa; Kronimus, Alexander; Schwarzbauer, Jan

(Savez hemijskih inženjera, Beograd, 2012)

TY  - JOUR
AU  - Antić, Vesna
AU  - Antić, Mališa
AU  - Kronimus, Alexander
AU  - Schwarzbauer, Jan
PY  - 2012
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/2920
AB  - 'On-line' pyrolysis coupled with gas chromatography (GC) was performed for quantitative determination of poly(vinylpyrrolidone) (PVP) in wastewater sample. Gas chromatography-mass spectrometry (GC-MS) showed that the main product of pyrolysis of PVP, at high temperatures, was N-vinylpyrrolidone (NVP). After that, different amounts of commercial PVP were pyrolyzed in order to establish the correlation between the amount of generated NVP (its GC peak area) and the initial mass of pyrolyzed PVP. GC-FID analysis was used for construction of the calibration curve and for quantitative determination of PVP. Very good linear correlation was obtained between the area of NVP peak, generated during pyrolysis, and the initial mass of PVP (r2 = 0.998). Further, solutions of known concentration of PVP were prepared in destilled water ('spiked samples'). Spiked samples were preextracted with diethyl ether and n-hexane, after which the water-layer was evaporated and dissolved again in methanol. Analysis of pyrolysates of preextracted spiked samples showed that the 'recovery' of PVP was above 96 mass%. This finding suggested that pre-extraction could be applied to reduce the concentration of organic substances that could also be pyrolyzed, and thus hinder identification and quantitative determination of PVP, without significant loss of polymer. The sample of an industrial wastewater from Pančevo, Serbia was investigated in the last part of this work. The sample was preextracted in the same way as the spiked samples and than pyrolyzed. NVP was identified by GC-MS in obtained pyrolysate, which was the evidence that PVP was present in the wastewater sample. NVP was quantified on the basis of the peak area in GC-FID chromatogram, and than the concentration of PVP in wastewater sample was calculated based on calibration curve. Concentration of PVP in industrial wastewater amounted 2.5 mg/L.
AB  - U ovom radu je primenjena metoda 'on-line' pirolize u sprezi sa gasnom hromatografijom (GC) za kvantitativno određivanje poli(vinilpirolidona) (PVP) u uzorku otpadne vode. Najpre je gasnomhromatografsko-masenospektrometrijskom analizom (GC-MS) utvrđeno da pirolizom PVP na visokim temperaturama kao glavni proizvod degradacije nastaje monomer, N-vinilpirolidon (NVP). Nakon toga su različite količine komercijalnog PVP pirolizovane da bi se uspostavila korelacija između količine nastalog NVP i inicijalne mase pirolizovanog polimera. Za konstruisanje kalibracione krive i kvantitativno određivanje PVP u rastvorima poznate koncentracije u destilovanoj vodi ('spiked samples'), kao i u uzorku otpadne vode, korišćena je GC analiza. Analizom rastvora komercijalnog PVP poznate koncentracije ustanovljeno je da PVP 'recovery', nakon ekstrakcije n-heksanom i dietil-etrom, iznosi iznad 96 mas.%. U poslednjem delu rada ispitan je uzorak industrijske otpadne vode iz Pančeva, Srbija. Pokazano je da je PVP bio prisutan u otpadnoj vodi i da je njegova koncentracija bila daleko iznad uobičajenih koncentracija niskomolekularnih organskih zagađivača.
PB  - Savez hemijskih inženjera, Beograd
T2  - Hemijska industrija
T1  - Quantitative determination of poly(vinylpyrrolidone) by 'On-line' pyrolysis coupled with gas chromatography
T1  - Kvantitativno određivanje poli(vinilpirolidona) primenom 'On-line' pirolize kuplovane sa gasnom hromatografijom
EP  - 364
IS  - 3
SP  - 357
VL  - 66
DO  - 10.2298/HEMIND111114108A
ER  - 
@article{
author = "Antić, Vesna and Antić, Mališa and Kronimus, Alexander and Schwarzbauer, Jan",
year = "2012",
abstract = "'On-line' pyrolysis coupled with gas chromatography (GC) was performed for quantitative determination of poly(vinylpyrrolidone) (PVP) in wastewater sample. Gas chromatography-mass spectrometry (GC-MS) showed that the main product of pyrolysis of PVP, at high temperatures, was N-vinylpyrrolidone (NVP). After that, different amounts of commercial PVP were pyrolyzed in order to establish the correlation between the amount of generated NVP (its GC peak area) and the initial mass of pyrolyzed PVP. GC-FID analysis was used for construction of the calibration curve and for quantitative determination of PVP. Very good linear correlation was obtained between the area of NVP peak, generated during pyrolysis, and the initial mass of PVP (r2 = 0.998). Further, solutions of known concentration of PVP were prepared in destilled water ('spiked samples'). Spiked samples were preextracted with diethyl ether and n-hexane, after which the water-layer was evaporated and dissolved again in methanol. Analysis of pyrolysates of preextracted spiked samples showed that the 'recovery' of PVP was above 96 mass%. This finding suggested that pre-extraction could be applied to reduce the concentration of organic substances that could also be pyrolyzed, and thus hinder identification and quantitative determination of PVP, without significant loss of polymer. The sample of an industrial wastewater from Pančevo, Serbia was investigated in the last part of this work. The sample was preextracted in the same way as the spiked samples and than pyrolyzed. NVP was identified by GC-MS in obtained pyrolysate, which was the evidence that PVP was present in the wastewater sample. NVP was quantified on the basis of the peak area in GC-FID chromatogram, and than the concentration of PVP in wastewater sample was calculated based on calibration curve. Concentration of PVP in industrial wastewater amounted 2.5 mg/L., U ovom radu je primenjena metoda 'on-line' pirolize u sprezi sa gasnom hromatografijom (GC) za kvantitativno određivanje poli(vinilpirolidona) (PVP) u uzorku otpadne vode. Najpre je gasnomhromatografsko-masenospektrometrijskom analizom (GC-MS) utvrđeno da pirolizom PVP na visokim temperaturama kao glavni proizvod degradacije nastaje monomer, N-vinilpirolidon (NVP). Nakon toga su različite količine komercijalnog PVP pirolizovane da bi se uspostavila korelacija između količine nastalog NVP i inicijalne mase pirolizovanog polimera. Za konstruisanje kalibracione krive i kvantitativno određivanje PVP u rastvorima poznate koncentracije u destilovanoj vodi ('spiked samples'), kao i u uzorku otpadne vode, korišćena je GC analiza. Analizom rastvora komercijalnog PVP poznate koncentracije ustanovljeno je da PVP 'recovery', nakon ekstrakcije n-heksanom i dietil-etrom, iznosi iznad 96 mas.%. U poslednjem delu rada ispitan je uzorak industrijske otpadne vode iz Pančeva, Srbija. Pokazano je da je PVP bio prisutan u otpadnoj vodi i da je njegova koncentracija bila daleko iznad uobičajenih koncentracija niskomolekularnih organskih zagađivača.",
publisher = "Savez hemijskih inženjera, Beograd",
journal = "Hemijska industrija",
title = "Quantitative determination of poly(vinylpyrrolidone) by 'On-line' pyrolysis coupled with gas chromatography, Kvantitativno određivanje poli(vinilpirolidona) primenom 'On-line' pirolize kuplovane sa gasnom hromatografijom",
pages = "364-357",
number = "3",
volume = "66",
doi = "10.2298/HEMIND111114108A"
}
Antić, V., Antić, M., Kronimus, A.,& Schwarzbauer, J.. (2012). Quantitative determination of poly(vinylpyrrolidone) by 'On-line' pyrolysis coupled with gas chromatography. in Hemijska industrija
Savez hemijskih inženjera, Beograd., 66(3), 357-364.
https://doi.org/10.2298/HEMIND111114108A
Antić V, Antić M, Kronimus A, Schwarzbauer J. Quantitative determination of poly(vinylpyrrolidone) by 'On-line' pyrolysis coupled with gas chromatography. in Hemijska industrija. 2012;66(3):357-364.
doi:10.2298/HEMIND111114108A .
Antić, Vesna, Antić, Mališa, Kronimus, Alexander, Schwarzbauer, Jan, "Quantitative determination of poly(vinylpyrrolidone) by 'On-line' pyrolysis coupled with gas chromatography" in Hemijska industrija, 66, no. 3 (2012):357-364,
https://doi.org/10.2298/HEMIND111114108A . .
2
1
3

Degradation of methyl-phenanthrene isomers during bioremediation of soil contaminated by residual fuel oil

Novaković, Milan; Ramadan, Muftah Mohamed Ali; Šolević-Knudsen, Tatjana; Antić, Mališa; Beskoski, Vladimir; Gojgić-Cvijović, Gordana; Vrvić, Miroslav M.; Jovančićević, Branimir

(Springer Heidelberg, Heidelberg, 2012)

TY  - JOUR
AU  - Novaković, Milan
AU  - Ramadan, Muftah Mohamed Ali
AU  - Šolević-Knudsen, Tatjana
AU  - Antić, Mališa
AU  - Beskoski, Vladimir
AU  - Gojgić-Cvijović, Gordana
AU  - Vrvić, Miroslav M.
AU  - Jovančićević, Branimir
PY  - 2012
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/2977
AB  - Phenanthrene and methyl-phenanthrenes are major aromatic pollutants originating in particular from fuel oil. Phenanthrene is usually degraded faster than methyl-phenanthrenes under geological and environmental conditions. Here, we report a preferential and accelerated biodegradation of methyl-phenanthrenes versus phenanthrene in soil contaminated by fuel oil. The polluted soil was mixed with sawdust and sand to form a homogenized biopile. The biopile was continuously sprayed with microbial consortia isolated from crude oil-contaminated soil and treated by biosurfactants and nutritive substances for biostimulation. During a 6-month bioremediation experiment, a steady increase in the relative abundance of phenanthrene compared to methyl-phenathrenes was observed by gas chromatography-mass spectrometry. The increase was the highest for trimethyl-phenanthrenes, with a phenanthrene/trimethyl-phenanthrenes ratio increasing from 0.42 to 2.45. By contrast, the control, non-stimulated samples showed a ratio decrease from 0.85 to 0.11. Moreover, the results showed that the level of degradability depends on the number of methyl groups.
PB  - Springer Heidelberg, Heidelberg
T2  - Environmental Chemistry Letters
T1  - Degradation of methyl-phenanthrene isomers during bioremediation of soil contaminated by residual fuel oil
EP  - 294
IS  - 3
SP  - 287
VL  - 10
DO  - 10.1007/s10311-012-0354-6
ER  - 
@article{
author = "Novaković, Milan and Ramadan, Muftah Mohamed Ali and Šolević-Knudsen, Tatjana and Antić, Mališa and Beskoski, Vladimir and Gojgić-Cvijović, Gordana and Vrvić, Miroslav M. and Jovančićević, Branimir",
year = "2012",
abstract = "Phenanthrene and methyl-phenanthrenes are major aromatic pollutants originating in particular from fuel oil. Phenanthrene is usually degraded faster than methyl-phenanthrenes under geological and environmental conditions. Here, we report a preferential and accelerated biodegradation of methyl-phenanthrenes versus phenanthrene in soil contaminated by fuel oil. The polluted soil was mixed with sawdust and sand to form a homogenized biopile. The biopile was continuously sprayed with microbial consortia isolated from crude oil-contaminated soil and treated by biosurfactants and nutritive substances for biostimulation. During a 6-month bioremediation experiment, a steady increase in the relative abundance of phenanthrene compared to methyl-phenathrenes was observed by gas chromatography-mass spectrometry. The increase was the highest for trimethyl-phenanthrenes, with a phenanthrene/trimethyl-phenanthrenes ratio increasing from 0.42 to 2.45. By contrast, the control, non-stimulated samples showed a ratio decrease from 0.85 to 0.11. Moreover, the results showed that the level of degradability depends on the number of methyl groups.",
publisher = "Springer Heidelberg, Heidelberg",
journal = "Environmental Chemistry Letters",
title = "Degradation of methyl-phenanthrene isomers during bioremediation of soil contaminated by residual fuel oil",
pages = "294-287",
number = "3",
volume = "10",
doi = "10.1007/s10311-012-0354-6"
}
Novaković, M., Ramadan, M. M. A., Šolević-Knudsen, T., Antić, M., Beskoski, V., Gojgić-Cvijović, G., Vrvić, M. M.,& Jovančićević, B.. (2012). Degradation of methyl-phenanthrene isomers during bioremediation of soil contaminated by residual fuel oil. in Environmental Chemistry Letters
Springer Heidelberg, Heidelberg., 10(3), 287-294.
https://doi.org/10.1007/s10311-012-0354-6
Novaković M, Ramadan MMA, Šolević-Knudsen T, Antić M, Beskoski V, Gojgić-Cvijović G, Vrvić MM, Jovančićević B. Degradation of methyl-phenanthrene isomers during bioremediation of soil contaminated by residual fuel oil. in Environmental Chemistry Letters. 2012;10(3):287-294.
doi:10.1007/s10311-012-0354-6 .
Novaković, Milan, Ramadan, Muftah Mohamed Ali, Šolević-Knudsen, Tatjana, Antić, Mališa, Beskoski, Vladimir, Gojgić-Cvijović, Gordana, Vrvić, Miroslav M., Jovančićević, Branimir, "Degradation of methyl-phenanthrene isomers during bioremediation of soil contaminated by residual fuel oil" in Environmental Chemistry Letters, 10, no. 3 (2012):287-294,
https://doi.org/10.1007/s10311-012-0354-6 . .
8
8
8