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Aerobic Biodegradation Studies of Nonylphenol Ethoxylates in River Water Using Liquid Chromatography−Electrospray Tandem Mass Spectrometry

The aerobic biodegradation of nonylphenol ethoxylates (A9PEO) was kinetically investigated in a laboratory-scale bioreactor filled with river water, spiked at a concentration of 10 mg L-1 nonionic surfactants. Analyses of the samples applying liquid chromatography−electrospray mass spectrometry (LC−...

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Bibliographic Details
Published in:Environmental science & technology 2001-01, Vol.35 (2), p.335-340
Main Authors: Jonkers, Niels, Knepper, Thomas P, de Voogt, Pim
Format: Article
Language:English
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Summary:The aerobic biodegradation of nonylphenol ethoxylates (A9PEO) was kinetically investigated in a laboratory-scale bioreactor filled with river water, spiked at a concentration of 10 mg L-1 nonionic surfactants. Analyses of the samples applying liquid chromatography−electrospray mass spectrometry (LC−ES-MS) after solid-phase enrichment revealed a relatively fast primary degradation of A9PEO with >99% degradation observed after 4 days. Contrary to the generally proposed degradation pathway of EO chain shortening, it could be shown that the initiating step of the degradation is ω-carboxylation of the individual ethoxylate chains:  metabolites with long carboxylated EO chains are identified (A9PEC). Further degradation proceeds gradually into short-chain carboxylated EO with the most abundant species being A9PE2C. The oxidation of the nonyl chain proceeds concomitantly with this degradation, leading to metabolites having both a carboxylated ethoxylate and an alkyl chain of varying lengths (CAPEC). The identity of the CAPEC metabolites was confirmed by the fragmentation pattern obtained with LC−ES-MS/MS. Both A9PEC and CAPEC metabolites are still present in the bioreactor after 31 days. In the aerobic degradation pathway, A9PEO2 is formed only to a minor extent and is even further degraded in several days. The endocrine disruptor nonylphenol was not found as a metabolite in this study.
ISSN:0013-936X
1520-5851
DOI:10.1021/es000127o