完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.author | Lin, JG | en_US |
dc.contributor.author | Ma, YS | en_US |
dc.date.accessioned | 2014-12-08T15:45:45Z | - |
dc.date.available | 2014-12-08T15:45:45Z | - |
dc.date.issued | 2000-02-01 | en_US |
dc.identifier.issn | 0733-9372 | en_US |
dc.identifier.uri | http://dx.doi.org/10.1061/(ASCE)0733-9372(2000)126:2(130) | en_US |
dc.identifier.uri | http://hdl.handle.net/11536/30773 | - |
dc.description.abstract | One 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.iso | en_US | en_US |
dc.title | Oxidation of 2-chlorophenol in water by ultrasound/Fenton method | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1061/(ASCE)0733-9372(2000)126:2(130) | en_US |
dc.identifier.journal | JOURNAL OF ENVIRONMENTAL ENGINEERING-ASCE | en_US |
dc.citation.volume | 126 | en_US |
dc.citation.issue | 2 | en_US |
dc.citation.spage | 130 | en_US |
dc.citation.epage | 137 | en_US |
dc.contributor.department | 環境工程研究所 | zh_TW |
dc.contributor.department | Institute of Environmental Engineering | en_US |
dc.identifier.wosnumber | WOS:000084860700007 | - |
dc.citation.woscount | 50 | - |
顯示於類別: | 期刊論文 |