| Project/Area Number |
16310064
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Environmental technology/Environmental materials
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| Research Institution | National Institute of Advanced Industrial Science and Technology (AIST) |
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Principal Investigator |
FUKUSHIMA Masami National Institute of Advanced Industrial Science and Technology, Institute for Environmental Management Technology, Senior Researcher, 環境管理技術研究部門, 主任研究員 (40344113)
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| Project Period (FY) |
2004 – 2005
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| Project Status |
Completed (Fiscal Year 2005)
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| Budget Amount *help |
¥9,100,000 (Direct Cost: ¥9,100,000)
Fiscal Year 2005: ¥2,600,000 (Direct Cost: ¥2,600,000)
Fiscal Year 2004: ¥6,500,000 (Direct Cost: ¥6,500,000)
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| Keywords | Iron(III)-porphyrin catalyst / Humic substances / Chlorinated organic compounds / Catalytic oxidation / Cyclodextrin / Supramolecular complex / Enhanced oxidation / 自己分解 / 有機塩素化合物 / 錯形成 |
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| Research Abstract |
The decrease of catalytic activity of an iron(III)-porphyrin catalyst (Fe-Por) can be attributed to self-degradation of Fe-Por. To prevent the self-degradation, we first examined the addition of hydroxypropyl-β-cyclodextrin (HP-β-CD) that is regarded as a model of hydrophobic parts in humic substances (HSs). The self-degradation of Fe-Por was suppressed by forming supramolecular complex between Fe-Por and HP-β-CD, and this resulted in enhancing oxidative degradation of pentachlorophenol (PCP). Second, the effects of HSs on the enhancement of peroxosulfate oxidation of PCP by Fe-Por were studied mechanistically. The addition of HSs was also effective in suppressing the self-degradation of Fe-Por and resulted in an enhanced PCP oxidation. ^1H NMR studies of D_2O solutions of Fe-Por, HSs and mixtures there of showed that the aromatic moieties in HSs contributed to the binding of the sulfonatophenyl groups in Fe-Por. Third, an HS was separated according to molecular size using size exclusion chromatography. Three fractions were obtained and their aromatic carbons were determined by solid-state CPMS ^<13>C NMR. The rate of self-degradation of Fe-Por decreased with increasing the content of aromatic carbon in the fractionated HS. In addition, formation constant of supramolecular complex between Fe-Por and fractionated HS increased with increasing the aromaticity of HS sample. This supports that formation of supramolecular complex is due to interactions between sulfonatophenyl groups in Fe-Por and aromatic moieties in the HS. These results led to a conclusion that function of HS for enhancing peroxosulfate oxidation of PCP by Fe-Por can be attributed to stabilization of the catalyst by forming supramolecular complex.
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