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dc.contributor.authorZailiang Liu
dc.contributor.authorHailing Meng
dc.contributor.authorChao Li
dc.contributor.authorHui Zhang
dc.contributor.authorJiashun Cao
dc.contributor.authorGuanhua Meng
dc.date.accessioned2022-01-30T19:27:23Z
dc.date.available2022-01-30T19:27:23Z
dc.date.issued2020
dc.identifier.other%28ASCE%29EE.1943-7870.0001653.pdf
dc.identifier.urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4265332
dc.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.
dc.publisherASCE
dc.titleDegradation of Biologically Treated Coking Wastewater over CuOx/PAC, CuOx/GAC, and CuOx/ACF Catalysts under Microwave Irradiation in the Presence of H2O2
dc.typeJournal Paper
dc.journal.volume146
dc.journal.issue4
dc.journal.titleJournal of Environmental Engineering
dc.identifier.doi10.1061/(ASCE)EE.1943-7870.0001653
dc.page04020014
dc.treeJournal of Environmental Engineering:;2020:;Volume ( 146 ):;issue: 004
dc.contenttypeFulltext


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