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dc.contributor.authorJunru Bu
dc.contributor.authorXinkai Zhou
dc.contributor.authorHuan Liu
dc.contributor.authorChunmian Lin
dc.date.accessioned2022-01-30T19:27:33Z
dc.date.available2022-01-30T19:27:33Z
dc.date.issued2020
dc.identifier.other%28ASCE%29EE.1943-7870.0001660.pdf
dc.identifier.urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4265338
dc.description.abstractThe roles of H2O2 in supercritical water oxidation (SCWO) were investigated. The results showed that some of the H2O2 could persist for a short time in SCW, and organic pollutants were mainly oxidized by the O2 generated from the H2O2 in SCWO. However, the introduction of Fe2+ into the SCWO system with H2O2 formed a new Fenton oxidation environment, i.e., supercritical Fenton oxidation (SCFO), which showed the cooperative effect of Fenton oxidation and SCWO. Comparative experiments of phenol and p-aminophenol (PAP) in SCWO and SCFO, respectively, were carried out. The results showed that, in the SCFO system, the CO2 yield from the oxidative degradation of phenol-simulated wastewater (766.0  mg/L) in 45s could reach 73.3%, much higher than that in the SCWO (49.2%) under the same conditions. After 8 min, the CO2 yield in SCFO (97.4%) was also significantly higher than that in SCWO (89.4%). The degradation efficiency of PAP-simulated wastewater (272.5  mg/L) in the SCFO system exceeded 94.3%, especially under acidic conditions, and the degradation efficiency reached 97.4%, much higher than that in the SCWO system (86.2%).
dc.publisherASCE
dc.titleSupercritical Fenton Oxidation: New Advanced Oxidation Technology
dc.typeJournal Paper
dc.journal.volume146
dc.journal.issue4
dc.journal.titleJournal of Environmental Engineering
dc.identifier.doi10.1061/(ASCE)EE.1943-7870.0001660
dc.page04020019
dc.treeJournal of Environmental Engineering:;2020:;Volume ( 146 ):;issue: 004
dc.contenttypeFulltext


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