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dc.contributor.authorLin, JGen_US
dc.contributor.authorMa, YSen_US
dc.date.accessioned2014-12-08T15:45:45Z-
dc.date.available2014-12-08T15:45:45Z-
dc.date.issued2000-02-01en_US
dc.identifier.issn0733-9372en_US
dc.identifier.urihttp://dx.doi.org/10.1061/(ASCE)0733-9372(2000)126:2(130)en_US
dc.identifier.urihttp://hdl.handle.net/11536/30773-
dc.description.abstractOne of the toxic and refractory pollutants formed during the color removal of fertilizer, chemical, and petroleum industrial effluents by chlorine is 2-chlorophenol (2-cp). The objective of this study is to investigate the effect of H2O2 and Fe2+ dosages on the decomposition of 2-cp using a coupled ultrasound/Fe2+/H2O2 process. The extent of 2-cp decomposition and mineralization depends on the dosages of H2O2 and Fe2+. More than 99% of 2-cp was decomposed and 86% of 2-cp was mineralized using the ultrasound/Fe2+/H2O2 process at Fe2+ of 10 mg/L and H2O2 of 500 mg/L. Oxidation-reduction potential (ORP) monitoring is a useful method for determining the decomposition efficiency of the target compound. There was a slight increase in the ORP values with increasing Fe2+ dosages, and an apparent increase with increasing H2O2 dosages was observed. The major intermediate formed during the decomposition of 2-cp was 2-chloro-p-benzoquinone. It was also readily decomposed using the coupled ultrasound/Fe2+/H2O2 process.en_US
dc.language.isoen_USen_US
dc.titleOxidation of 2-chlorophenol in water by ultrasound/Fenton methoden_US
dc.typeArticleen_US
dc.identifier.doi10.1061/(ASCE)0733-9372(2000)126:2(130)en_US
dc.identifier.journalJOURNAL OF ENVIRONMENTAL ENGINEERING-ASCEen_US
dc.citation.volume126en_US
dc.citation.issue2en_US
dc.citation.spage130en_US
dc.citation.epage137en_US
dc.contributor.department環境工程研究所zh_TW
dc.contributor.departmentInstitute of Environmental Engineeringen_US
dc.identifier.wosnumberWOS:000084860700007-
dc.citation.woscount50-
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