Babić, Biljana

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637f655b-27fe-4a7f-937d-110587b05540
  • Babić, Biljana (2)
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Author's Bibliography

Removal of heavy metals from aqueous solution using natural and fe(iii) oxyhydroxide clinoptilolite

Milićević, Sonja; Milošević, Vladan; Povrenović, Dragan; Stojanović, Jovica; Martinović, Sanja; Babić, Biljana

(Springer, New York, 2013)

TY  - JOUR
AU  - Milićević, Sonja
AU  - Milošević, Vladan
AU  - Povrenović, Dragan
AU  - Stojanović, Jovica
AU  - Martinović, Sanja
AU  - Babić, Biljana
PY  - 2013
UR  - https://ritnms.itnms.ac.rs/handle/123456789/262
AB  - The increasing levels of industrial wastewater released to the environment present a serious threat to human health, living resources, and ecological systems. Fe-modified zeolites were developed and tested for removal of Cu2+ and Zn2+ from contaminated water. The surfaces of the naturally occurring zeolite, clinoptilolite, were modified with Fe(III) oxyhydroxides using three different methods, denoted I, II, and III (FeCli(1), FeCli(2), and FeNaCli(1), respectively). The oxyhydroxides were prepared in Method I using 0.1 M FeCl3 center dot 6H(2)O in an acetate buffer (pH = 3.6); in Method II, using 10% FeCl3 center dot 6H(2)O solution in 0.1 M KOH (pH = 10); and Method III was the same as Method I except the clinoptilolite was pretreated with NaCl. Newly synthesized materials from these three methods were then tested for their ability to enhance the sorption capacity for Cu and Zn compared to the natural sample (Cli). Powder X-ray diffraction measurements and the chemical composition of these modified samples confirmed that clinoptilolite maintained its structure while amorphous Fe3+ species were synthesized. The specific surface area (BET method) of both the natural and modified clinoptilolite increased by 2 and 7.5 times for Methods I and II, respectively. Scanning electron microscopy and energy dispersive X-ray spectroscopy revealed that CaO was formed during Method I (FeCli(1)). Throughout the adsorption process, the hydrolysis of CaO and the release of OH- caused the precipitation of Cu and Zn hydroxide, which made the determination of the sorption capacity of FeCli(1) impossible. This phenomenon was avoided in Method III (FeNaCli(1)) because of the absence of exchangeable Ca2+. The adsorption experiments with Method II resulted in double-enchanced adsoprtion capacity. Laboratory batch experiments revealed that the sorption capacities increased in the following order: Cli  LT  FeCli(2)  LT  FeNaCli(1), for Cu: 0.121 mmol/g  LT  0.251 mmol/g  LT  0.403 mmol/g and for Zn: 0.128 mmol/g  LT  0.234 mmol/g  LT  0.381 mmol/g.
PB  - Springer, New York
T2  - Clays and Clay Minerals
T1  - Removal of heavy metals from aqueous solution using natural and fe(iii) oxyhydroxide clinoptilolite
EP  - 516
IS  - 6
SP  - 508
VL  - 61
DO  - 10.1346/CCMN.2013.0610603
UR  - conv_696
ER  - 
@article{
author = "Milićević, Sonja and Milošević, Vladan and Povrenović, Dragan and Stojanović, Jovica and Martinović, Sanja and Babić, Biljana",
year = "2013",
abstract = "The increasing levels of industrial wastewater released to the environment present a serious threat to human health, living resources, and ecological systems. Fe-modified zeolites were developed and tested for removal of Cu2+ and Zn2+ from contaminated water. The surfaces of the naturally occurring zeolite, clinoptilolite, were modified with Fe(III) oxyhydroxides using three different methods, denoted I, II, and III (FeCli(1), FeCli(2), and FeNaCli(1), respectively). The oxyhydroxides were prepared in Method I using 0.1 M FeCl3 center dot 6H(2)O in an acetate buffer (pH = 3.6); in Method II, using 10% FeCl3 center dot 6H(2)O solution in 0.1 M KOH (pH = 10); and Method III was the same as Method I except the clinoptilolite was pretreated with NaCl. Newly synthesized materials from these three methods were then tested for their ability to enhance the sorption capacity for Cu and Zn compared to the natural sample (Cli). Powder X-ray diffraction measurements and the chemical composition of these modified samples confirmed that clinoptilolite maintained its structure while amorphous Fe3+ species were synthesized. The specific surface area (BET method) of both the natural and modified clinoptilolite increased by 2 and 7.5 times for Methods I and II, respectively. Scanning electron microscopy and energy dispersive X-ray spectroscopy revealed that CaO was formed during Method I (FeCli(1)). Throughout the adsorption process, the hydrolysis of CaO and the release of OH- caused the precipitation of Cu and Zn hydroxide, which made the determination of the sorption capacity of FeCli(1) impossible. This phenomenon was avoided in Method III (FeNaCli(1)) because of the absence of exchangeable Ca2+. The adsorption experiments with Method II resulted in double-enchanced adsoprtion capacity. Laboratory batch experiments revealed that the sorption capacities increased in the following order: Cli  LT  FeCli(2)  LT  FeNaCli(1), for Cu: 0.121 mmol/g  LT  0.251 mmol/g  LT  0.403 mmol/g and for Zn: 0.128 mmol/g  LT  0.234 mmol/g  LT  0.381 mmol/g.",
publisher = "Springer, New York",
journal = "Clays and Clay Minerals",
title = "Removal of heavy metals from aqueous solution using natural and fe(iii) oxyhydroxide clinoptilolite",
pages = "516-508",
number = "6",
volume = "61",
doi = "10.1346/CCMN.2013.0610603",
url = "conv_696"
}
Milićević, S., Milošević, V., Povrenović, D., Stojanović, J., Martinović, S.,& Babić, B.. (2013). Removal of heavy metals from aqueous solution using natural and fe(iii) oxyhydroxide clinoptilolite. in Clays and Clay Minerals
Springer, New York., 61(6), 508-516.
https://doi.org/10.1346/CCMN.2013.0610603
conv_696
Milićević S, Milošević V, Povrenović D, Stojanović J, Martinović S, Babić B. Removal of heavy metals from aqueous solution using natural and fe(iii) oxyhydroxide clinoptilolite. in Clays and Clay Minerals. 2013;61(6):508-516.
doi:10.1346/CCMN.2013.0610603
conv_696 .
Milićević, Sonja, Milošević, Vladan, Povrenović, Dragan, Stojanović, Jovica, Martinović, Sanja, Babić, Biljana, "Removal of heavy metals from aqueous solution using natural and fe(iii) oxyhydroxide clinoptilolite" in Clays and Clay Minerals, 61, no. 6 (2013):508-516,
https://doi.org/10.1346/CCMN.2013.0610603 .,
conv_696 .
12
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Removal of copper from aqueous solutions by low cost adsorbent-Kolubara lignite

Milićević, Sonja; Boljanac, Tamara; Martinović, Sanja; Vlahović, Milica; Milošević, Vladan; Babić, Biljana

(Elsevier Science Bv, Amsterdam, 2012)

TY  - JOUR
AU  - Milićević, Sonja
AU  - Boljanac, Tamara
AU  - Martinović, Sanja
AU  - Vlahović, Milica
AU  - Milošević, Vladan
AU  - Babić, Biljana
PY  - 2012
UR  - https://ritnms.itnms.ac.rs/handle/123456789/206
AB  - Serbian lignite from "Kolubara" deposit was used as a low cost adsorbent for removal of copper ions (Cu2+) from aqueous solutions. Lignite was subjected to the elementary and technical analysis as well as BET and FTIR analysis due to complete characterization. Basic comparison between lignite and activated carbon was also done. As a method, batch adsorption procedure was applied. Adsorption efficiency was studied as a function of the initial metal concentration, pH of the solution, contact time, and amount of the adsorbent. Optimum removal of copper ions was achieved at pH values of 5.0. About 90% of copper cations were removed in 5 min of contact time from the solution with the lowest copper concentration (50 mg Cu2+/l) regardless adsorbent amount, while the same effect of adsorption was achieved in 60 min in case of solutions with higher concentrations of copper. It was concluded that the effect of adsorbent amount on adsorption kinetics is evident but not crucial. It was proved that the experimental results of copper adsorption fit well to a Langmuirian type isotherm which was used to describe monitored adsorption phenomena. The calculated adsorption capacities of lignite for copper adsorption decrease with increasing adsorbent amount. The study proved that tested lignite is very efficient adsorbent material, especially in case of low copper concentration in aqueous solution where the usual methods are either economically unrewarding or technically complicated. This behavior can be explained by FTIR spectrum despite a small specific surface area of lignite. Namely, many bands (peaks) are attributed to the functional groups that they are involved in chemisorption and ionic exchange, basic mechanisms of copper adsorption.
PB  - Elsevier Science Bv, Amsterdam
T2  - Fuel Processing Technology
T1  - Removal of copper from aqueous solutions by low cost adsorbent-Kolubara lignite
EP  - 7
SP  - 1
VL  - 95
DO  - 10.1016/j.fuproc.2011.11.005
UR  - conv_615
ER  - 
@article{
author = "Milićević, Sonja and Boljanac, Tamara and Martinović, Sanja and Vlahović, Milica and Milošević, Vladan and Babić, Biljana",
year = "2012",
abstract = "Serbian lignite from "Kolubara" deposit was used as a low cost adsorbent for removal of copper ions (Cu2+) from aqueous solutions. Lignite was subjected to the elementary and technical analysis as well as BET and FTIR analysis due to complete characterization. Basic comparison between lignite and activated carbon was also done. As a method, batch adsorption procedure was applied. Adsorption efficiency was studied as a function of the initial metal concentration, pH of the solution, contact time, and amount of the adsorbent. Optimum removal of copper ions was achieved at pH values of 5.0. About 90% of copper cations were removed in 5 min of contact time from the solution with the lowest copper concentration (50 mg Cu2+/l) regardless adsorbent amount, while the same effect of adsorption was achieved in 60 min in case of solutions with higher concentrations of copper. It was concluded that the effect of adsorbent amount on adsorption kinetics is evident but not crucial. It was proved that the experimental results of copper adsorption fit well to a Langmuirian type isotherm which was used to describe monitored adsorption phenomena. The calculated adsorption capacities of lignite for copper adsorption decrease with increasing adsorbent amount. The study proved that tested lignite is very efficient adsorbent material, especially in case of low copper concentration in aqueous solution where the usual methods are either economically unrewarding or technically complicated. This behavior can be explained by FTIR spectrum despite a small specific surface area of lignite. Namely, many bands (peaks) are attributed to the functional groups that they are involved in chemisorption and ionic exchange, basic mechanisms of copper adsorption.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Fuel Processing Technology",
title = "Removal of copper from aqueous solutions by low cost adsorbent-Kolubara lignite",
pages = "7-1",
volume = "95",
doi = "10.1016/j.fuproc.2011.11.005",
url = "conv_615"
}
Milićević, S., Boljanac, T., Martinović, S., Vlahović, M., Milošević, V.,& Babić, B.. (2012). Removal of copper from aqueous solutions by low cost adsorbent-Kolubara lignite. in Fuel Processing Technology
Elsevier Science Bv, Amsterdam., 95, 1-7.
https://doi.org/10.1016/j.fuproc.2011.11.005
conv_615
Milićević S, Boljanac T, Martinović S, Vlahović M, Milošević V, Babić B. Removal of copper from aqueous solutions by low cost adsorbent-Kolubara lignite. in Fuel Processing Technology. 2012;95:1-7.
doi:10.1016/j.fuproc.2011.11.005
conv_615 .
Milićević, Sonja, Boljanac, Tamara, Martinović, Sanja, Vlahović, Milica, Milošević, Vladan, Babić, Biljana, "Removal of copper from aqueous solutions by low cost adsorbent-Kolubara lignite" in Fuel Processing Technology, 95 (2012):1-7,
https://doi.org/10.1016/j.fuproc.2011.11.005 .,
conv_615 .
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