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    Degradation of Biologically Treated Coking Wastewater over CuOx/PAC, CuOx/GAC, and CuOx/ACF Catalysts under Microwave Irradiation in the Presence of H2O2

    Source: Journal of Environmental Engineering:;2020:;Volume ( 146 ):;issue: 004
    Author:
    Zailiang Liu
    ,
    Hailing Meng
    ,
    Chao Li
    ,
    Hui Zhang
    ,
    Jiashun Cao
    ,
    Guanhua Meng
    DOI: 10.1061/(ASCE)EE.1943-7870.0001653
    Publisher: ASCE
    Abstract: In this work, we adopted the impregnating-baking method to prepare CuOx/granular activated carbon (GAC), CuOx/activated carbon fiber (ACF), and CuOx/powdery activated carbon (PAC) catalysts whose physicochemical properties were then investigated. The catalytic activities of the synthesized catalysts for degrading biologically treated coking wastewater (BTCW) were studied during the microwave-catalytic wet peroxide oxidation (MW-CWPO) process. The results showed that the catalytic activities were in the order of CuOx/PAC>CuOx/ACF>CuOx/GAC. When the catalyst and hydrogen peroxide (H2O2) dosage is (2  g/L, 0.9  mL/L), (3  g/L, 4  mL/L), and (15  g/L, 10  mL/L), the degradation efficiency is approximately 86.4%, 80.9%, and 78.8% for CuOx/PAC, CuOx/ACF, and CuOx/GAC, respectively. The enhanced catalytic activity of CuOx/PAC can be attributed to greater adsorption and “hot spot” generation as well as sufficient contact among the catalyst, H2O2, and organics in aqueous solution resulting from its large specific surface area and small particle size. The hydroxyl radical (•OH) is proved to be the main active free radical based on free radical scavenging. The catalysts showed limited stability due to the leaching of Cu and catalyst crumble down, which poses an important challenge.
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      Degradation of Biologically Treated Coking Wastewater over CuOx/PAC, CuOx/GAC, and CuOx/ACF Catalysts under Microwave Irradiation in the Presence of H2O2

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    contributor authorZailiang Liu
    contributor authorHailing Meng
    contributor authorChao Li
    contributor authorHui Zhang
    contributor authorJiashun Cao
    contributor authorGuanhua Meng
    date accessioned2022-01-30T19:27:23Z
    date available2022-01-30T19:27:23Z
    date issued2020
    identifier other%28ASCE%29EE.1943-7870.0001653.pdf
    identifier urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4265332
    description abstractIn this work, we adopted the impregnating-baking method to prepare CuOx/granular activated carbon (GAC), CuOx/activated carbon fiber (ACF), and CuOx/powdery activated carbon (PAC) catalysts whose physicochemical properties were then investigated. The catalytic activities of the synthesized catalysts for degrading biologically treated coking wastewater (BTCW) were studied during the microwave-catalytic wet peroxide oxidation (MW-CWPO) process. The results showed that the catalytic activities were in the order of CuOx/PAC>CuOx/ACF>CuOx/GAC. When the catalyst and hydrogen peroxide (H2O2) dosage is (2  g/L, 0.9  mL/L), (3  g/L, 4  mL/L), and (15  g/L, 10  mL/L), the degradation efficiency is approximately 86.4%, 80.9%, and 78.8% for CuOx/PAC, CuOx/ACF, and CuOx/GAC, respectively. The enhanced catalytic activity of CuOx/PAC can be attributed to greater adsorption and “hot spot” generation as well as sufficient contact among the catalyst, H2O2, and organics in aqueous solution resulting from its large specific surface area and small particle size. The hydroxyl radical (•OH) is proved to be the main active free radical based on free radical scavenging. The catalysts showed limited stability due to the leaching of Cu and catalyst crumble down, which poses an important challenge.
    publisherASCE
    titleDegradation of Biologically Treated Coking Wastewater over CuOx/PAC, CuOx/GAC, and CuOx/ACF Catalysts under Microwave Irradiation in the Presence of H2O2
    typeJournal Paper
    journal volume146
    journal issue4
    journal titleJournal of Environmental Engineering
    identifier doi10.1061/(ASCE)EE.1943-7870.0001653
    page04020014
    treeJournal of Environmental Engineering:;2020:;Volume ( 146 ):;issue: 004
    contenttypeFulltext
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