Photocatalytic reduction of nitrate in seawater using C/TiO2 nanoparticles
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作者:
Shaban, Yasser A.
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King Abdulaziz Univ, Marine Chem Dept, Fac Marine Sci, POB 80207, Jeddah 21589, Saudi Arabia
Natl Inst Oceanog & Fisheries, Alexandria, EgyptKing Abdulaziz Univ, Marine Chem Dept, Fac Marine Sci, POB 80207, Jeddah 21589, Saudi Arabia
Shaban, Yasser A.
[1
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El Maradny, Amr A.
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King Abdulaziz Univ, Marine Chem Dept, Fac Marine Sci, POB 80207, Jeddah 21589, Saudi Arabia
Natl Inst Oceanog & Fisheries, Alexandria, EgyptKing Abdulaziz Univ, Marine Chem Dept, Fac Marine Sci, POB 80207, Jeddah 21589, Saudi Arabia
El Maradny, Amr A.
[1
,2
]
Al Farawati, Radwan Kh.
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King Abdulaziz Univ, Marine Chem Dept, Fac Marine Sci, POB 80207, Jeddah 21589, Saudi ArabiaKing Abdulaziz Univ, Marine Chem Dept, Fac Marine Sci, POB 80207, Jeddah 21589, Saudi Arabia
Al Farawati, Radwan Kh.
[1
]
机构:
[1] King Abdulaziz Univ, Marine Chem Dept, Fac Marine Sci, POB 80207, Jeddah 21589, Saudi Arabia
This study investigates the photocatalytic reduction of nitrate in seawater using carbon-modified titanium oxide (C/TiO2) nanoparticles under different reaction conditions. Formic acid was used as a sacrificial electron donor for inhibiting the mechanism of electron/hole recombination on the photocatalyst. Unmodified titanium oxide (TiO2) and reference TiO2 P25 photocatalysts were used for comparison. The elemental composition determined through energy dispersive spectroscopy (EDS) analysis evidenced the carbon modification for C/TiO2 nanoparticles. The optical bandgap energy for C/TiO2 has been remarkably reduced to 1.78 eV which in turn enhanced its performance towards the photocatalytic removal of nitrate under ultraviolet as well as natural sunlight irradiation. Factors including C/TiO2 loading, initial nitrate concentration, solution pH and hole scavenger concentration were studied to attain the optimal reaction conditions. The highest nitrate photocatalytic removal rate was obtained at catalyst loading of 0.5 g L-1, pH 3 and 0.04 M of formic acid. The kinetic study showed that the photocatalytic nitrate removal from seawater using carbon-modified titanium oxide was successfully expressed by the pseudo first-order reaction kinetics. (C) 2016 Elsevier B.V. All rights reserved.
机构:
Silpakorn Univ, Fac Engn & Ind Technol, Dept Mat Sci & Engn, Bangkok 10330, ThailandSilpakorn Univ, Fac Engn & Ind Technol, Dept Mat Sci & Engn, Bangkok 10330, Thailand
Jarunsak, Natnapin
Chuangchai, Thirawich
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Silpakorn Univ, Fac Engn & Ind Technol, Dept Mat Sci & Engn, Bangkok 10330, ThailandSilpakorn Univ, Fac Engn & Ind Technol, Dept Mat Sci & Engn, Bangkok 10330, Thailand
Chuangchai, Thirawich
Buasri, Achanai
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Silpakorn Univ, Fac Engn & Ind Technol, Dept Mat Sci & Engn, Bangkok 10330, Thailand
Natl Ctr Excellence Petr Petrochem & Adv Mat, Bangkok 10330, ThailandSilpakorn Univ, Fac Engn & Ind Technol, Dept Mat Sci & Engn, Bangkok 10330, Thailand
机构:
UNSJ, Inst Invest Mineras, CONICET, Fac Ingn, Av Libertador San Martin 1109 O, RA-5400 San Juan, ArgentinaUNSJ, Inst Invest Mineras, CONICET, Fac Ingn, Av Libertador San Martin 1109 O, RA-5400 San Juan, Argentina
Maratta, Ariel
Villafane, Gaston
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UNSJ, Inst Invest Mineras, CONICET, Fac Ingn, Av Libertador San Martin 1109 O, RA-5400 San Juan, ArgentinaUNSJ, Inst Invest Mineras, CONICET, Fac Ingn, Av Libertador San Martin 1109 O, RA-5400 San Juan, Argentina
Villafane, Gaston
Brandaleze, Elena
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UTN Fac Reg San Nicolas, Colon 332,B2900LWH, Buenos Aires, DF, ArgentinaUNSJ, Inst Invest Mineras, CONICET, Fac Ingn, Av Libertador San Martin 1109 O, RA-5400 San Juan, Argentina
Brandaleze, Elena
Pacheco, Pablo
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CONICET UNSL, Ctr Cient Tecnol San Luis CCT San Luis, INQUISAL, RA-5700 San Luis, ArgentinaUNSJ, Inst Invest Mineras, CONICET, Fac Ingn, Av Libertador San Martin 1109 O, RA-5400 San Juan, Argentina
Pacheco, Pablo
Bazan, Vanesa
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UNSJ, Inst Invest Mineras, CONICET, Fac Ingn, Av Libertador San Martin 1109 O, RA-5400 San Juan, ArgentinaUNSJ, Inst Invest Mineras, CONICET, Fac Ingn, Av Libertador San Martin 1109 O, RA-5400 San Juan, Argentina
机构:University of Szeged,Reaction Kinetics Research Group, Chemical Research Centre of the Hungarian Academy of Sciences, Department of Physical Chemistry and Materials Science
Gy. Halasi
A. Kecskeméti
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机构:University of Szeged,Reaction Kinetics Research Group, Chemical Research Centre of the Hungarian Academy of Sciences, Department of Physical Chemistry and Materials Science
A. Kecskeméti
F. Solymosi
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机构:University of Szeged,Reaction Kinetics Research Group, Chemical Research Centre of the Hungarian Academy of Sciences, Department of Physical Chemistry and Materials Science