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DDT-Related Compounds Bound to the Nonextractable Particulate Matter in Sediments of the Teltow Canal, Germany

Authors :
Ralf Littke
Jan Schwarzbauer
Mathias Ricking
Source :
Environmental Science & Technology. 37:488-495
Publication Year :
2003
Publisher :
American Chemical Society (ACS), 2003.

Abstract

Sediment samples of the Teltow Canal (Berlin, Germany) were analyzed with respect to extractable and nonextractable organic compounds. The study focused on the identification and quantitation of bound 2,2-bis(chlorophenyl)-1,1,1-trichlorethane (DDT) residues in order to obtain further information about the fate of DDT-derived compounds within the particulate matter of the aquatic environment. Various chemical degradation techniques and a complementary online pyrolysis-GC/MS method were applied to the pre-extracted sediment residues. Generally, the distribution of the bound DDT-related compounds was found to differ distinctly from the substances distribution within the extractable fraction. The main metabolite of the anaerobic degradation pathway (2,2-bis(chlorophenyl)-1,1-dichlorethane, DDD) is most abundant in the sediment extracts but occurred only in insignificant concentrations in the degradation products of all procedures applied. The most abundant DDT-metabolites released after the degradation procedures were 4,4'-DBP, 4,4'-DDA, and 4,4'-DDM. In addition, 4,4'-DDM was detected at rather high concentrations by pyrolytic analysis. The results imply a weak association to the nonextractable particulate matter based on noncovalent interactions for the observed DDT-related contaminants. The release of these compounds was initiated by the modification and degradation of the organic macromolecular matrix as well as of the inorganic material. Furthermore, numerous methoxychlor-related compounds were detected not only in the extracts but also in parts of the hydrolysis products.

Details

ISSN :
15205851 and 0013936X
Volume :
37
Database :
OpenAIRE
Journal :
Environmental Science & Technology
Accession number :
edsair.doi.dedup.....35ab15335946d9f203b351044f24ab5e
Full Text :
https://doi.org/10.1021/es0201451