Physics of nanostructured oxide materials and strongly correlated systems

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Physics of nanostructured oxide materials and strongly correlated systems (en)
Физика наноструктурних оксидних материјала и јако корелисаних система (sr)
Fizika nanostrukturnih oksidnih materijala i jako korelisanih sistema (sr_RS)
Authors

Publications

Nitrate-assisted photocatalytic efficiency of defective Eu-doped Pr(OH)(3) nanostructures

Aškrabić, S.; Araujo, V. D.; Passacantando, M.; Bernardi, M. I. B.; Tomić, N.; Dojčinović, Biljana P.; Manojlović, Dragan D.; Čalija, B.; Miletić, M.; Dohčević-Mitrović, Z. D.

(Royal Soc Chemistry, Cambridge, 2017)

TY  - JOUR
AU  - Aškrabić, S.
AU  - Araujo, V. D.
AU  - Passacantando, M.
AU  - Bernardi, M. I. B.
AU  - Tomić, N.
AU  - Dojčinović, Biljana P.
AU  - Manojlović, Dragan D.
AU  - Čalija, B.
AU  - Miletić, M.
AU  - Dohčević-Mitrović, Z. D.
PY  - 2017
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2561
AB  - Pr(OH)(3) one-dimensional nanostructures are a less studied member of lanthanide hydroxide nanostructures, which recently demonstrated an excellent adsorption capacity for organic pollutant removal from wastewater. In this study, Pr1-xEux(OH)(3) (x = 0, 0.01, 0.03, and 0.05) defective nanostructures were synthesized by a facile and scalable microwave-assisted hydrothermal method using KOH as an alkaline metal precursor. The phase and surface composition, morphology, vibrational, electronic and optical properties of the as-prepared samples were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), inductively coupled plasma optical emission spectrometry (ICP-OES), transmission electron microscopy (TEM), field emission scanning electron microscopy (FE-SEM), Raman, infrared (IR), photoluminescence (PL), and diffuse reflectance spectroscopy (DRS). It was deduced that the incorporation of Eu3+ ions promoted the formation of oxygen vacancies in the already defective Pr(OH)(3), subsequently changing the Pr(OH)(3) nanorod morphology. The presence of KNO3 phase was registered in the Eu-doped samples. The oxygendeficient Eu-doped Pr(OH)(3) nanostructures displayed an improved photocatalytic activity in the removal of reactive orange (RO16) dye under UV-vis light irradiation. An enhanced photocatalytic activity of the Eu-doped Pr(OH)(3) nanostructures was caused by the synergetic effect of oxygen vacancies and Eu3+ (NO3-) ions present on the Pr(OH)(3) surface, the charge separation efficiency and the formation of the reactive radicals. In addition, the 3% Eu-doped sample exhibited very good adsorptive properties due to different morphology and higher electrostatic attraction with the anionic dye. Pr1-xEux(OH)(3) nanostructures with the possibility of tuning their adsorption/photocatalytic properties present a great potential for wastewater treatment.
PB  - Royal Soc Chemistry, Cambridge
T2  - Physical Chemistry Chemical Physics
T1  - Nitrate-assisted photocatalytic efficiency of defective Eu-doped Pr(OH)(3) nanostructures
VL  - 19
IS  - 47
SP  - 31756
EP  - 31765
DO  - 10.1039/c7cp06440c
ER  - 
@article{
author = "Aškrabić, S. and Araujo, V. D. and Passacantando, M. and Bernardi, M. I. B. and Tomić, N. and Dojčinović, Biljana P. and Manojlović, Dragan D. and Čalija, B. and Miletić, M. and Dohčević-Mitrović, Z. D.",
year = "2017",
abstract = "Pr(OH)(3) one-dimensional nanostructures are a less studied member of lanthanide hydroxide nanostructures, which recently demonstrated an excellent adsorption capacity for organic pollutant removal from wastewater. In this study, Pr1-xEux(OH)(3) (x = 0, 0.01, 0.03, and 0.05) defective nanostructures were synthesized by a facile and scalable microwave-assisted hydrothermal method using KOH as an alkaline metal precursor. The phase and surface composition, morphology, vibrational, electronic and optical properties of the as-prepared samples were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), inductively coupled plasma optical emission spectrometry (ICP-OES), transmission electron microscopy (TEM), field emission scanning electron microscopy (FE-SEM), Raman, infrared (IR), photoluminescence (PL), and diffuse reflectance spectroscopy (DRS). It was deduced that the incorporation of Eu3+ ions promoted the formation of oxygen vacancies in the already defective Pr(OH)(3), subsequently changing the Pr(OH)(3) nanorod morphology. The presence of KNO3 phase was registered in the Eu-doped samples. The oxygendeficient Eu-doped Pr(OH)(3) nanostructures displayed an improved photocatalytic activity in the removal of reactive orange (RO16) dye under UV-vis light irradiation. An enhanced photocatalytic activity of the Eu-doped Pr(OH)(3) nanostructures was caused by the synergetic effect of oxygen vacancies and Eu3+ (NO3-) ions present on the Pr(OH)(3) surface, the charge separation efficiency and the formation of the reactive radicals. In addition, the 3% Eu-doped sample exhibited very good adsorptive properties due to different morphology and higher electrostatic attraction with the anionic dye. Pr1-xEux(OH)(3) nanostructures with the possibility of tuning their adsorption/photocatalytic properties present a great potential for wastewater treatment.",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "Physical Chemistry Chemical Physics",
title = "Nitrate-assisted photocatalytic efficiency of defective Eu-doped Pr(OH)(3) nanostructures",
volume = "19",
number = "47",
pages = "31756-31765",
doi = "10.1039/c7cp06440c"
}
Aškrabić, S., Araujo, V. D., Passacantando, M., Bernardi, M. I. B., Tomić, N., Dojčinović, B. P., Manojlović, D. D., Čalija, B., Miletić, M.,& Dohčević-Mitrović, Z. D.. (2017). Nitrate-assisted photocatalytic efficiency of defective Eu-doped Pr(OH)(3) nanostructures. in Physical Chemistry Chemical Physics
Royal Soc Chemistry, Cambridge., 19(47), 31756-31765.
https://doi.org/10.1039/c7cp06440c
Aškrabić S, Araujo VD, Passacantando M, Bernardi MIB, Tomić N, Dojčinović BP, Manojlović DD, Čalija B, Miletić M, Dohčević-Mitrović ZD. Nitrate-assisted photocatalytic efficiency of defective Eu-doped Pr(OH)(3) nanostructures. in Physical Chemistry Chemical Physics. 2017;19(47):31756-31765.
doi:10.1039/c7cp06440c .
Aškrabić, S., Araujo, V. D., Passacantando, M., Bernardi, M. I. B., Tomić, N., Dojčinović, Biljana P., Manojlović, Dragan D., Čalija, B., Miletić, M., Dohčević-Mitrović, Z. D., "Nitrate-assisted photocatalytic efficiency of defective Eu-doped Pr(OH)(3) nanostructures" in Physical Chemistry Chemical Physics, 19, no. 47 (2017):31756-31765,
https://doi.org/10.1039/c7cp06440c . .
6
6
6
5

Nitrate-assisted photocatalytic efficiency of defective Eu-doped Pr(OH)(3) nanostructures

Aškrabić, S.; Araujo, V. D.; Passacantando, M.; Bernardi, M. I. B.; Tomić, N.; Dojčinović, Biljana P.; Manojlović, Dragan D.; Čalija, B.; Miletić, M.; Dohčević-Mitrović, Z. D.

(Royal Soc Chemistry, Cambridge, 2017)

TY  - JOUR
AU  - Aškrabić, S.
AU  - Araujo, V. D.
AU  - Passacantando, M.
AU  - Bernardi, M. I. B.
AU  - Tomić, N.
AU  - Dojčinović, Biljana P.
AU  - Manojlović, Dragan D.
AU  - Čalija, B.
AU  - Miletić, M.
AU  - Dohčević-Mitrović, Z. D.
PY  - 2017
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2958
AB  - Pr(OH)(3) one-dimensional nanostructures are a less studied member of lanthanide hydroxide nanostructures, which recently demonstrated an excellent adsorption capacity for organic pollutant removal from wastewater. In this study, Pr1-xEux(OH)(3) (x = 0, 0.01, 0.03, and 0.05) defective nanostructures were synthesized by a facile and scalable microwave-assisted hydrothermal method using KOH as an alkaline metal precursor. The phase and surface composition, morphology, vibrational, electronic and optical properties of the as-prepared samples were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), inductively coupled plasma optical emission spectrometry (ICP-OES), transmission electron microscopy (TEM), field emission scanning electron microscopy (FE-SEM), Raman, infrared (IR), photoluminescence (PL), and diffuse reflectance spectroscopy (DRS). It was deduced that the incorporation of Eu3+ ions promoted the formation of oxygen vacancies in the already defective Pr(OH)(3), subsequently changing the Pr(OH)(3) nanorod morphology. The presence of KNO3 phase was registered in the Eu-doped samples. The oxygendeficient Eu-doped Pr(OH)(3) nanostructures displayed an improved photocatalytic activity in the removal of reactive orange (RO16) dye under UV-vis light irradiation. An enhanced photocatalytic activity of the Eu-doped Pr(OH)(3) nanostructures was caused by the synergetic effect of oxygen vacancies and Eu3+ (NO3-) ions present on the Pr(OH)(3) surface, the charge separation efficiency and the formation of the reactive radicals. In addition, the 3% Eu-doped sample exhibited very good adsorptive properties due to different morphology and higher electrostatic attraction with the anionic dye. Pr1-xEux(OH)(3) nanostructures with the possibility of tuning their adsorption/photocatalytic properties present a great potential for wastewater treatment.
PB  - Royal Soc Chemistry, Cambridge
T2  - Physical Chemistry Chemical Physics
T1  - Nitrate-assisted photocatalytic efficiency of defective Eu-doped Pr(OH)(3) nanostructures
VL  - 19
IS  - 47
SP  - 31756
EP  - 31765
DO  - 10.1039/c7cp06440c
ER  - 
@article{
author = "Aškrabić, S. and Araujo, V. D. and Passacantando, M. and Bernardi, M. I. B. and Tomić, N. and Dojčinović, Biljana P. and Manojlović, Dragan D. and Čalija, B. and Miletić, M. and Dohčević-Mitrović, Z. D.",
year = "2017",
abstract = "Pr(OH)(3) one-dimensional nanostructures are a less studied member of lanthanide hydroxide nanostructures, which recently demonstrated an excellent adsorption capacity for organic pollutant removal from wastewater. In this study, Pr1-xEux(OH)(3) (x = 0, 0.01, 0.03, and 0.05) defective nanostructures were synthesized by a facile and scalable microwave-assisted hydrothermal method using KOH as an alkaline metal precursor. The phase and surface composition, morphology, vibrational, electronic and optical properties of the as-prepared samples were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), inductively coupled plasma optical emission spectrometry (ICP-OES), transmission electron microscopy (TEM), field emission scanning electron microscopy (FE-SEM), Raman, infrared (IR), photoluminescence (PL), and diffuse reflectance spectroscopy (DRS). It was deduced that the incorporation of Eu3+ ions promoted the formation of oxygen vacancies in the already defective Pr(OH)(3), subsequently changing the Pr(OH)(3) nanorod morphology. The presence of KNO3 phase was registered in the Eu-doped samples. The oxygendeficient Eu-doped Pr(OH)(3) nanostructures displayed an improved photocatalytic activity in the removal of reactive orange (RO16) dye under UV-vis light irradiation. An enhanced photocatalytic activity of the Eu-doped Pr(OH)(3) nanostructures was caused by the synergetic effect of oxygen vacancies and Eu3+ (NO3-) ions present on the Pr(OH)(3) surface, the charge separation efficiency and the formation of the reactive radicals. In addition, the 3% Eu-doped sample exhibited very good adsorptive properties due to different morphology and higher electrostatic attraction with the anionic dye. Pr1-xEux(OH)(3) nanostructures with the possibility of tuning their adsorption/photocatalytic properties present a great potential for wastewater treatment.",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "Physical Chemistry Chemical Physics",
title = "Nitrate-assisted photocatalytic efficiency of defective Eu-doped Pr(OH)(3) nanostructures",
volume = "19",
number = "47",
pages = "31756-31765",
doi = "10.1039/c7cp06440c"
}
Aškrabić, S., Araujo, V. D., Passacantando, M., Bernardi, M. I. B., Tomić, N., Dojčinović, B. P., Manojlović, D. D., Čalija, B., Miletić, M.,& Dohčević-Mitrović, Z. D.. (2017). Nitrate-assisted photocatalytic efficiency of defective Eu-doped Pr(OH)(3) nanostructures. in Physical Chemistry Chemical Physics
Royal Soc Chemistry, Cambridge., 19(47), 31756-31765.
https://doi.org/10.1039/c7cp06440c
Aškrabić S, Araujo VD, Passacantando M, Bernardi MIB, Tomić N, Dojčinović BP, Manojlović DD, Čalija B, Miletić M, Dohčević-Mitrović ZD. Nitrate-assisted photocatalytic efficiency of defective Eu-doped Pr(OH)(3) nanostructures. in Physical Chemistry Chemical Physics. 2017;19(47):31756-31765.
doi:10.1039/c7cp06440c .
Aškrabić, S., Araujo, V. D., Passacantando, M., Bernardi, M. I. B., Tomić, N., Dojčinović, Biljana P., Manojlović, Dragan D., Čalija, B., Miletić, M., Dohčević-Mitrović, Z. D., "Nitrate-assisted photocatalytic efficiency of defective Eu-doped Pr(OH)(3) nanostructures" in Physical Chemistry Chemical Physics, 19, no. 47 (2017):31756-31765,
https://doi.org/10.1039/c7cp06440c . .
6
6
6
5

Supplementary data for article : Askrabic, S.; Araujo, V. D.; Passacantando, M.; Bernardi, M. I. B.; Tomic, N.; Dojčinović, B. P.; Manojlović, D. D.; Calija, B.; Miletic, M.; Dohcevic-Mitrovic, Z. D. Nitrate-Assisted Photocatalytic Efficiency of Defective Eu-Doped Pr(OH)(3) Nanostructures. Physical Chemistry Chemical Physics 2017, 19 (47), 31756–31765. https://doi.org/10.1039/c7cp06440c

Aškrabić, S.; Araujo, V. D.; Passacantando, M.; Bernardi, M. I. B.; Tomić, N.; Dojčinović, Biljana P.; Manojlović, Dragan D.; Čalija, B.; Miletić, M.; Dohčević-Mitrović, Z. D.

(Royal Soc Chemistry, Cambridge, 2017)

TY  - DATA
AU  - Aškrabić, S.
AU  - Araujo, V. D.
AU  - Passacantando, M.
AU  - Bernardi, M. I. B.
AU  - Tomić, N.
AU  - Dojčinović, Biljana P.
AU  - Manojlović, Dragan D.
AU  - Čalija, B.
AU  - Miletić, M.
AU  - Dohčević-Mitrović, Z. D.
PY  - 2017
PY  - 2017
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2959
PB  - Royal Soc Chemistry, Cambridge
T2  - Physical Chemistry Chemical Physics
T1  - Supplementary data for article :       Askrabic, S.; Araujo, V. D.; Passacantando, M.; Bernardi, M. I. B.; Tomic, N.; Dojčinović, B. P.; Manojlović, D. D.; Calija, B.; Miletic, M.; Dohcevic-Mitrovic, Z. D. Nitrate-Assisted Photocatalytic Efficiency of Defective Eu-Doped Pr(OH)(3) Nanostructures. Physical Chemistry Chemical Physics 2017, 19 (47), 31756–31765. https://doi.org/10.1039/c7cp06440c
UR  - https://hdl.handle.net/21.15107/rcub_cherry_2959
ER  - 
@misc{
author = "Aškrabić, S. and Araujo, V. D. and Passacantando, M. and Bernardi, M. I. B. and Tomić, N. and Dojčinović, Biljana P. and Manojlović, Dragan D. and Čalija, B. and Miletić, M. and Dohčević-Mitrović, Z. D.",
year = "2017, 2017",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "Physical Chemistry Chemical Physics",
title = "Supplementary data for article :       Askrabic, S.; Araujo, V. D.; Passacantando, M.; Bernardi, M. I. B.; Tomic, N.; Dojčinović, B. P.; Manojlović, D. D.; Calija, B.; Miletic, M.; Dohcevic-Mitrovic, Z. D. Nitrate-Assisted Photocatalytic Efficiency of Defective Eu-Doped Pr(OH)(3) Nanostructures. Physical Chemistry Chemical Physics 2017, 19 (47), 31756–31765. https://doi.org/10.1039/c7cp06440c",
url = "https://hdl.handle.net/21.15107/rcub_cherry_2959"
}
Aškrabić, S., Araujo, V. D., Passacantando, M., Bernardi, M. I. B., Tomić, N., Dojčinović, B. P., Manojlović, D. D., Čalija, B., Miletić, M.,& Dohčević-Mitrović, Z. D.. (2017). Supplementary data for article :       Askrabic, S.; Araujo, V. D.; Passacantando, M.; Bernardi, M. I. B.; Tomic, N.; Dojčinović, B. P.; Manojlović, D. D.; Calija, B.; Miletic, M.; Dohcevic-Mitrovic, Z. D. Nitrate-Assisted Photocatalytic Efficiency of Defective Eu-Doped Pr(OH)(3) Nanostructures. Physical Chemistry Chemical Physics 2017, 19 (47), 31756–31765. https://doi.org/10.1039/c7cp06440c. in Physical Chemistry Chemical Physics
Royal Soc Chemistry, Cambridge..
https://hdl.handle.net/21.15107/rcub_cherry_2959
Aškrabić S, Araujo VD, Passacantando M, Bernardi MIB, Tomić N, Dojčinović BP, Manojlović DD, Čalija B, Miletić M, Dohčević-Mitrović ZD. Supplementary data for article :       Askrabic, S.; Araujo, V. D.; Passacantando, M.; Bernardi, M. I. B.; Tomic, N.; Dojčinović, B. P.; Manojlović, D. D.; Calija, B.; Miletic, M.; Dohcevic-Mitrovic, Z. D. Nitrate-Assisted Photocatalytic Efficiency of Defective Eu-Doped Pr(OH)(3) Nanostructures. Physical Chemistry Chemical Physics 2017, 19 (47), 31756–31765. https://doi.org/10.1039/c7cp06440c. in Physical Chemistry Chemical Physics. 2017;.
https://hdl.handle.net/21.15107/rcub_cherry_2959 .
Aškrabić, S., Araujo, V. D., Passacantando, M., Bernardi, M. I. B., Tomić, N., Dojčinović, Biljana P., Manojlović, Dragan D., Čalija, B., Miletić, M., Dohčević-Mitrović, Z. D., "Supplementary data for article :       Askrabic, S.; Araujo, V. D.; Passacantando, M.; Bernardi, M. I. B.; Tomic, N.; Dojčinović, B. P.; Manojlović, D. D.; Calija, B.; Miletic, M.; Dohcevic-Mitrovic, Z. D. Nitrate-Assisted Photocatalytic Efficiency of Defective Eu-Doped Pr(OH)(3) Nanostructures. Physical Chemistry Chemical Physics 2017, 19 (47), 31756–31765. https://doi.org/10.1039/c7cp06440c" in Physical Chemistry Chemical Physics (2017),
https://hdl.handle.net/21.15107/rcub_cherry_2959 .

Адсорпциона и фотокаталитичка својства наноматеријала на бази церијум(IV) оксида и титан(IV) оксида

Tomić, Nataša M.

(Универзитет у Београду, Хемијски факултет, 2017)

TY  - THES
AU  - Tomić, Nataša M.
PY  - 2017
UR  - http://eteze.bg.ac.rs/application/showtheses?thesesId=5731
UR  - https://fedorabg.bg.ac.rs/fedora/get/o:17552/bdef:Content/download
UR  - http://vbs.rs/scripts/cobiss?command=DISPLAY&base=70036&RID=50003983
UR  - http://nardus.mpn.gov.rs/123456789/9357
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2763
AB  - Циљ овог истраживања је синтеза различитих облика наноструктурних прахова, базираних на оксидима церијума и титанијума, као и анализа њихових структурних, електронских, морфолошких и текстуралних особина како би се испитао њихов утицај на могућу примену ових нанопрахова као адсорбената и/или фотокатализатора за различите органске боје. Први део тезе укључује испитивање различито синтетисаних нанопрахова CeO2, док се други део тезе односи на проучавање нанопрахова базираних на TiO2, са акцентом на недовољно испитану брукитну фазу. Карактеризација добијених материјала и њихове адсорпционе/фотокаталитичке особине испитане су дифракцијом рендгенског зрачења на праху, раманском спектроскопијом, инфрацрвеном спектроскопијом са фуријеовом трансформацијом, скенирајућом електронском микроскопијом, методом физисорпције азота, елипсометријом, термогравиметријском методом и УЉ/ВИС спектроскопијом.Нанопрахови CeO2 синтетисани су коришћењем три начина синтезе: самопропагирајућом синтезом на собној температури (CeO2-δ-S), хидротермалном методом (CeO2-δ-H) и методом преципитације (CeO2-δ-P). Испитиван је утицај синтезе на адсорпциона и фотокаталитичка својства коришћењем три различите азо боје: Reactive Orange 16 (RO16), Methyl Orange (MO) и Mordant Blue 9 (MB9). Нанопрах CeO2−δ-S, синтетисан брзом и ефикасном самопропагирајућом методом, пронађен је као врло ефикасан адсорбент за боје и може бити обећавајући материјал у третману отпадних вода. Овај нанопрах је показао сличне адсорпционе особине када је у питању МО боја, у поређењу са комерцијалним активним угљеником, док CeO2−δ-S показује још бољу адсорпциону способност од активног угљеника за RO16 боју. На основу адсорпционих изотерми за узорак CeO2−δ-S, показано је да Лангмиров модел мало боље описује изотерме за МО и RO16, док се Фројндлиховим моделом боље фитују подаци када је у питању изотерма за MB9 у целом опсегу концентрација. Одређене су и вредности максималних адсорпционих капацитета нанопраха CeO2−δ-S за све три боје. Утврђен је и предложен механизам адсорпционог процеса нанопраха CeO2−δ-S,који је базиран на информацијама добијеним из инфрацрвених спектара и експериментално одређене вредности тачке нултог наелектрисања (pHZPC). Формирање бидентатног моста између сулфонских група и Ce4+ катјона, као и протонизација површинских хидроксилних група церијум-диоксида сматрају се одговорним за ефикасност адсорпционог процеса. Показано је такође да адсорпциони процес церијум-диоксида прати кинетички модел псеудо-другог реда, што подразумева да поред јаке електростатичке интеракције, хемисорпција игра кључну улогу у адсорпцији боја. С друге стране, нанопрахови CeO2-δ-H и CeO2-δ-P су показали одсуство адсорпције за азо боје. Међутим, њихова фотокаталитичка активност испитана је кроз деградацију азо боје RO16, при чему је разлика у њиховој активности корелисана са разликом у електронској структури и димензијама кристалита...
AB  - The aim of this thesis is to synthesize the various forms of nanostructured powders, based on cerium- and titanium- oxides, and to analyze as well their structural, electronic, morphological, and textural properties in order to examine their influence on potential application of these materials as adsorbents and/or photocatalysts for different organic dyes. The first part of the thesis includes examination of different synthesized nanocrystalline powders of CeO2, while the second part deals with the study of the nanopowders based on TiO2, with emphasize on the insufficiently known and examined brookite phase. Characterization of synthesized powders and their adsorption/photocatalytic properties is done by X-ray diffraction method, Raman spectroscopy, Fourier transform infrared Spectroscopy, Scanning electronic microscopy, N2 physisorption measurements, Ellipsometry, Thermogravimetric analysis and UV/VIS spectroscopy.CeO2 nanopowders are synthesized using three different methods such as self-propagating room temperature (CeO2-δ-S), hydrothermal (CeO2-δ-H) and precipitation method (CeO2-δ-P). The effect of preparation procedure on the adsorption and photocatalytic properties is investigated by using three synthetic azo dyes such as Reactive Orange 16 (RO16), Methyl Orange (MO), and Mordant Blue 9 (MB9). The CeO2−δ-S nanopowder, synthesized by a facile and cost effective SPRT method, is found to be an effective dye adsorbent and can be a promising substitute in wastewater treatment. In comparison to commercial powdered activated carbon (AC), adsorption properties of CeO2−δ-S for MO dye are found to be similar, whereas the CeO2−δ-S demonstrates even better adsorption capability than AC for RO16 dye. By studying the equilibrium adsorption data for CeO2−δ-S, it is shown that the Langmuir model slightly better describes isotherm data for MO and RO16, while the Freundlich model is a better fit for MB9 over the whole concentration range. The maximum adsorption capacities of CeO2−δ-S for all three dyes were measured. The mechanism of CeO2−δ adsorption process, mostly based on the information derived from the Infrared spectra andexperimentally determined value for Zero Point Charge (pHZPC), is established and proposed. The formation of a bidentate type bridge between sulfonate group and Ce4+ cations and the protonation of ceria surface hydroxyls is found to be responsible for effective adsorption process. It is also shown that the adsorption process follows the pseudo-second-order kinetic model, indicating that besides the strong electrostatic interaction, chemisorption plays an important role for the dye adsorption. On the other hand, the absence of adsorption of both CeO2-δ-H and CeO2-δ-P powders is found. However, their photocatalytic activity toward RO16 azo dye is examined, while the difference in their activity is correlated to difference in their electronic structure and crystallite size...
PB  - Универзитет у Београду, Хемијски факултет
T2  - Универзитет у Београду
T1  - Адсорпциона и фотокаталитичка својства наноматеријала на бази церијум(IV) оксида и титан(IV) оксида
UR  - https://hdl.handle.net/21.15107/rcub_nardus_9357
ER  - 
@phdthesis{
author = "Tomić, Nataša M.",
year = "2017",
abstract = "Циљ овог истраживања је синтеза различитих облика наноструктурних прахова, базираних на оксидима церијума и титанијума, као и анализа њихових структурних, електронских, морфолошких и текстуралних особина како би се испитао њихов утицај на могућу примену ових нанопрахова као адсорбената и/или фотокатализатора за различите органске боје. Први део тезе укључује испитивање различито синтетисаних нанопрахова CeO2, док се други део тезе односи на проучавање нанопрахова базираних на TiO2, са акцентом на недовољно испитану брукитну фазу. Карактеризација добијених материјала и њихове адсорпционе/фотокаталитичке особине испитане су дифракцијом рендгенског зрачења на праху, раманском спектроскопијом, инфрацрвеном спектроскопијом са фуријеовом трансформацијом, скенирајућом електронском микроскопијом, методом физисорпције азота, елипсометријом, термогравиметријском методом и УЉ/ВИС спектроскопијом.Нанопрахови CeO2 синтетисани су коришћењем три начина синтезе: самопропагирајућом синтезом на собној температури (CeO2-δ-S), хидротермалном методом (CeO2-δ-H) и методом преципитације (CeO2-δ-P). Испитиван је утицај синтезе на адсорпциона и фотокаталитичка својства коришћењем три различите азо боје: Reactive Orange 16 (RO16), Methyl Orange (MO) и Mordant Blue 9 (MB9). Нанопрах CeO2−δ-S, синтетисан брзом и ефикасном самопропагирајућом методом, пронађен је као врло ефикасан адсорбент за боје и може бити обећавајући материјал у третману отпадних вода. Овај нанопрах је показао сличне адсорпционе особине када је у питању МО боја, у поређењу са комерцијалним активним угљеником, док CeO2−δ-S показује још бољу адсорпциону способност од активног угљеника за RO16 боју. На основу адсорпционих изотерми за узорак CeO2−δ-S, показано је да Лангмиров модел мало боље описује изотерме за МО и RO16, док се Фројндлиховим моделом боље фитују подаци када је у питању изотерма за MB9 у целом опсегу концентрација. Одређене су и вредности максималних адсорпционих капацитета нанопраха CeO2−δ-S за све три боје. Утврђен је и предложен механизам адсорпционог процеса нанопраха CeO2−δ-S,који је базиран на информацијама добијеним из инфрацрвених спектара и експериментално одређене вредности тачке нултог наелектрисања (pHZPC). Формирање бидентатног моста између сулфонских група и Ce4+ катјона, као и протонизација површинских хидроксилних група церијум-диоксида сматрају се одговорним за ефикасност адсорпционог процеса. Показано је такође да адсорпциони процес церијум-диоксида прати кинетички модел псеудо-другог реда, што подразумева да поред јаке електростатичке интеракције, хемисорпција игра кључну улогу у адсорпцији боја. С друге стране, нанопрахови CeO2-δ-H и CeO2-δ-P су показали одсуство адсорпције за азо боје. Међутим, њихова фотокаталитичка активност испитана је кроз деградацију азо боје RO16, при чему је разлика у њиховој активности корелисана са разликом у електронској структури и димензијама кристалита..., The aim of this thesis is to synthesize the various forms of nanostructured powders, based on cerium- and titanium- oxides, and to analyze as well their structural, electronic, morphological, and textural properties in order to examine their influence on potential application of these materials as adsorbents and/or photocatalysts for different organic dyes. The first part of the thesis includes examination of different synthesized nanocrystalline powders of CeO2, while the second part deals with the study of the nanopowders based on TiO2, with emphasize on the insufficiently known and examined brookite phase. Characterization of synthesized powders and their adsorption/photocatalytic properties is done by X-ray diffraction method, Raman spectroscopy, Fourier transform infrared Spectroscopy, Scanning electronic microscopy, N2 physisorption measurements, Ellipsometry, Thermogravimetric analysis and UV/VIS spectroscopy.CeO2 nanopowders are synthesized using three different methods such as self-propagating room temperature (CeO2-δ-S), hydrothermal (CeO2-δ-H) and precipitation method (CeO2-δ-P). The effect of preparation procedure on the adsorption and photocatalytic properties is investigated by using three synthetic azo dyes such as Reactive Orange 16 (RO16), Methyl Orange (MO), and Mordant Blue 9 (MB9). The CeO2−δ-S nanopowder, synthesized by a facile and cost effective SPRT method, is found to be an effective dye adsorbent and can be a promising substitute in wastewater treatment. In comparison to commercial powdered activated carbon (AC), adsorption properties of CeO2−δ-S for MO dye are found to be similar, whereas the CeO2−δ-S demonstrates even better adsorption capability than AC for RO16 dye. By studying the equilibrium adsorption data for CeO2−δ-S, it is shown that the Langmuir model slightly better describes isotherm data for MO and RO16, while the Freundlich model is a better fit for MB9 over the whole concentration range. The maximum adsorption capacities of CeO2−δ-S for all three dyes were measured. The mechanism of CeO2−δ adsorption process, mostly based on the information derived from the Infrared spectra andexperimentally determined value for Zero Point Charge (pHZPC), is established and proposed. The formation of a bidentate type bridge between sulfonate group and Ce4+ cations and the protonation of ceria surface hydroxyls is found to be responsible for effective adsorption process. It is also shown that the adsorption process follows the pseudo-second-order kinetic model, indicating that besides the strong electrostatic interaction, chemisorption plays an important role for the dye adsorption. On the other hand, the absence of adsorption of both CeO2-δ-H and CeO2-δ-P powders is found. However, their photocatalytic activity toward RO16 azo dye is examined, while the difference in their activity is correlated to difference in their electronic structure and crystallite size...",
publisher = "Универзитет у Београду, Хемијски факултет",
journal = "Универзитет у Београду",
title = "Адсорпциона и фотокаталитичка својства наноматеријала на бази церијум(IV) оксида и титан(IV) оксида",
url = "https://hdl.handle.net/21.15107/rcub_nardus_9357"
}
Tomić, N. M.. (2017). Адсорпциона и фотокаталитичка својства наноматеријала на бази церијум(IV) оксида и титан(IV) оксида. in Универзитет у Београду
Универзитет у Београду, Хемијски факултет..
https://hdl.handle.net/21.15107/rcub_nardus_9357
Tomić NM. Адсорпциона и фотокаталитичка својства наноматеријала на бази церијум(IV) оксида и титан(IV) оксида. in Универзитет у Београду. 2017;.
https://hdl.handle.net/21.15107/rcub_nardus_9357 .
Tomić, Nataša M., "Адсорпциона и фотокаталитичка својства наноматеријала на бази церијум(IV) оксида и титан(IV) оксида" in Универзитет у Београду (2017),
https://hdl.handle.net/21.15107/rcub_nardus_9357 .