完整後設資料紀錄
DC 欄位語言
dc.contributor.authorLu, MCen_US
dc.contributor.authorRoam, GDen_US
dc.contributor.authorChen, JNen_US
dc.contributor.authorHuang, CPen_US
dc.date.accessioned2014-12-08T15:03:38Z-
dc.date.available2014-12-08T15:03:38Z-
dc.date.issued1995en_US
dc.identifier.issn0098-6445en_US
dc.identifier.urihttp://hdl.handle.net/11536/2167-
dc.identifier.urihttp://dx.doi.org/10.1080/00986449508936394en_US
dc.description.abstractPhotocatalytic oxidation process can be an effective method for the removal of toxic organic compounds from dilute aqueous solutions. Three toxic compounds, namely, dichlorvos (an insecticide), propoxur (an insecticide), and 2, 4-D (a herbicide), were used as the model compounds for the mineralization experiments. Total organic carbon measurements were used to measure the extent and the rate of the mineralization of these toxic chemicals. Additionally, ions such as chloride, phosphate and ammonia were also measured during the photomineralization reaction. Results show that the photocatalytic system is effective in mineralizing these pesticides. Both pH and the initial concentration of the organic compounds affect the mineralization reaction. The mineralization reaction is favored under an acid condition and increases with increasing initial organic concentration. The initial rate of the photomineralization reaction can be described by a Langmuir-Hinshelwood expression.en_US
dc.language.isoen_USen_US
dc.subjectphotocatalyticen_US
dc.subjectmineralizationen_US
dc.subjecttoxic chemicalsen_US
dc.titlePhotocatalytic mineralization of toxic chemicals with illuminated TiO2en_US
dc.typeArticleen_US
dc.identifier.doi10.1080/00986449508936394en_US
dc.identifier.journalCHEMICAL ENGINEERING COMMUNICATIONSen_US
dc.citation.volume139en_US
dc.citation.spage1en_US
dc.citation.epage13en_US
dc.contributor.department環境工程研究所zh_TW
dc.contributor.departmentInstitute of Environmental Engineeringen_US
dc.identifier.wosnumberWOS:A1995UM06100001-
dc.citation.woscount19-
顯示於類別:期刊論文