| Hauptseite > Publikationsdatenbank > Degradation of a chiral nonylphenol isomer in two agricultural soils |
| Journal Article | PreJuSER-4117 |
; ; ; ;
2009
Elsevier Science
Amsterdam [u.a.]
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Please use a persistent id in citations: doi:10.1016/j.envpol.2009.01.026
Abstract: The degradation of a chiral nonylphenol isomer, 4-(1-ethyl-1,4-dimethylpentyl)phenol (NP(112)), in two agricultural soils from Monheim and Dortmund, Germany has been studied. The degradation of NP(112) and the formation of a nitro-nonylphenol metabolite were determined by means of GC-MS analysis. The degradation followed bi-exponential order kinetics, with half-life of less than 5 days in both soils. The nitro-metabolite was found at different concentration levels in the two soils. The nitro-metabolite of NP(112) was more persistent than its parent compound. After 150 days about 13% of the initially applied NP(112) remained in the Monheim soil as its nitro-metabolite. Results of the E-screen assay revealed that the nitro-NP(112) has oestrogenic potency of 85% of that of NP(112). Furthermore, the results of chiral GC-MS analysis revealed that no chiral degradation of NP(112) occurred in this study.
Keyword(s): Agriculture (MeSH) ; Biodegradation, Environmental (MeSH) ; Ecology: methods (MeSH) ; Endocrine Disruptors: analysis (MeSH) ; Gas Chromatography-Mass Spectrometry (MeSH) ; Germany (MeSH) ; Half-Life (MeSH) ; Hydrogen-Ion Concentration (MeSH) ; Models, Chemical (MeSH) ; Phenols: analysis (MeSH) ; Soil: analysis (MeSH) ; Soil Microbiology (MeSH) ; Stereoisomerism (MeSH) ; Endocrine Disruptors ; Phenols ; Soil ; nonylphenol ; J ; Nitro-NP (auto) ; Persistent metabolite (auto) ; Estrogenic potency (auto) ; E-screen (auto) ; Chiral GC-MS (auto)
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