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    Enhancement of the Catalytic Ozonation Process by Using TiO<sub>2</sub>/ZrO<sub>2</sub> Nanoparticles

    Source: Journal of Hazardous, Toxic, and Radioactive Waste:;2024:;Volume ( 028 ):;issue: 004::page 04024018-1
    Author:
    Thom Thi Dang
    ,
    Manh Tuan Duong
    ,
    Long Huu Tran
    ,
    Manh Van Do
    ,
    Tuyen Van Trinh
    DOI: 10.1061/JHTRBP.HZENG-1313
    Publisher: American Society of Civil Engineers
    Abstract: In this study, we employed synthesized titanium oxide/zirconium oxide (TiO2/ZrO2) nanoparticles as activated catalysts to enhance the ozonation process during hydroxyl radical (OH°) generation using atrazine (ATZ) as a pollutant. The TiO2/ZrO2 nanoparticles were synthesized using the coprecipitation digestion method and were characterized using scanning and transmission electron microscopy, X-ray diffraction, Brunauer–Emmett–Teller theory, and energy dispersive X-ray spectroscopy. The experiments were conducted under different initial pH conditions (3, 7, and 10), with an initial ATZ concentration of 4.64 × 10−6 M, initial TiO2/ZrO2 nanocatalyst concentrations of 100, 200, and 300 ppm, and initial ozone (O3) concentrations of 1.35 × 10−4, 1.55 × 10−4, and 2.27 × 10−4 M, respectively. The key operational parameters were optimized, and the optimal OH° results were obtained at pH 10, 200 ppm TiO2/ZrO2 concentration, 4.64 × 10−6 M ATZ concentration, and 1.55 × 10−4 M O3 concentration. The potential of TiO2/ZrO2 nanoparticles to enhance OH° generation during catalytic ozonation was demonstrated. The catalytic ozonation mechanism using TiO2/ZrO2 nanoparticles was governed by the optimal formation of OH° radicals at about 1 × 10−11 mol/L and an excellent nanocatalytic activity with an Rct value of 2.83 × 10−8.
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      Enhancement of the Catalytic Ozonation Process by Using TiO<sub>2</sub>/ZrO<sub>2</sub> Nanoparticles

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    contributor authorThom Thi Dang
    contributor authorManh Tuan Duong
    contributor authorLong Huu Tran
    contributor authorManh Van Do
    contributor authorTuyen Van Trinh
    date accessioned2024-12-24T10:29:44Z
    date available2024-12-24T10:29:44Z
    date copyright10/1/2024 12:00:00 AM
    date issued2024
    identifier otherJHTRBP.HZENG-1313.pdf
    identifier urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4299027
    description abstractIn this study, we employed synthesized titanium oxide/zirconium oxide (TiO2/ZrO2) nanoparticles as activated catalysts to enhance the ozonation process during hydroxyl radical (OH°) generation using atrazine (ATZ) as a pollutant. The TiO2/ZrO2 nanoparticles were synthesized using the coprecipitation digestion method and were characterized using scanning and transmission electron microscopy, X-ray diffraction, Brunauer–Emmett–Teller theory, and energy dispersive X-ray spectroscopy. The experiments were conducted under different initial pH conditions (3, 7, and 10), with an initial ATZ concentration of 4.64 × 10−6 M, initial TiO2/ZrO2 nanocatalyst concentrations of 100, 200, and 300 ppm, and initial ozone (O3) concentrations of 1.35 × 10−4, 1.55 × 10−4, and 2.27 × 10−4 M, respectively. The key operational parameters were optimized, and the optimal OH° results were obtained at pH 10, 200 ppm TiO2/ZrO2 concentration, 4.64 × 10−6 M ATZ concentration, and 1.55 × 10−4 M O3 concentration. The potential of TiO2/ZrO2 nanoparticles to enhance OH° generation during catalytic ozonation was demonstrated. The catalytic ozonation mechanism using TiO2/ZrO2 nanoparticles was governed by the optimal formation of OH° radicals at about 1 × 10−11 mol/L and an excellent nanocatalytic activity with an Rct value of 2.83 × 10−8.
    publisherAmerican Society of Civil Engineers
    titleEnhancement of the Catalytic Ozonation Process by Using TiO2/ZrO2 Nanoparticles
    typeJournal Article
    journal volume28
    journal issue4
    journal titleJournal of Hazardous, Toxic, and Radioactive Waste
    identifier doi10.1061/JHTRBP.HZENG-1313
    journal fristpage04024018-1
    journal lastpage04024018-9
    page9
    treeJournal of Hazardous, Toxic, and Radioactive Waste:;2024:;Volume ( 028 ):;issue: 004
    contenttypeFulltext
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    DSpace software copyright © 2002-2015  DuraSpace
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