Record number :
Title of article :
Vertical distribution profiles and diagenetic fate of synthetic surfactants in marine and freshwater sediments Original Research Article
Author/Authors :
Carmen Corada-Fern?ndez، نويسنده , , Pablo A. Lara-Mart?n، نويسنده , , Lucila Candela a، نويسنده , , Eduardo Gonz?lez-Mazo، نويسنده ,
Issue Information :
دوهفته نامه با شماره پیاپی سال 2013
Pages :
From page :
To page :
Abstract :
This manuscript deals with the presence and degradation of the most commonly-used surfactants, including anionic (linear alkylbenzene sulfonates, LAS, and alkyl ethoxysulfates, AES) and non-ionic (alcohol polyethoxylates, AEOs, and nonylphenol polyethoxylates, NPEOs) compounds, in sediments and pore water from several aquatic environments (Southwest, Spain). Different vertical distributions were observed according to the respective sources, uses, production volumes and physicochemical properties of each surfactant. Levels of nonionics (up to 10 mg kg− 1) were twice as high as anionics in industrial areas and harbors, whereas the opposite was found near urban wastewater discharge outlets. Sulfophenyl carboxylic acids (SPCs), LAS degradation products, were identified at anoxic depths at some sampling stations. Their presence was related to in situ anaerobic degradation of LAS in marine sediments, whereas the occurrence of these metabolites in freshwater sediments was attributed to the existence of wastewater sources nearby. No significant changes in the average length of AEO and NPEO ethoxylated chains were observed along the sediment cores, suggesting that their biodegradation was very limited in the sampling area. This may be directly related to their lower bioavailability, as their calculated sediment–pore water distribution coefficients (log Ksw), which showed that non-ionic surfactants examined in this study had greater sorption affinity than the anionic surfactants (e.g., 2.3 ± 0.3 for NPEOs).
Keywords :
Surfactants , Pore water , Sorption , sediment , Estuaries , Degradation
Journal title :
Science of the Total Environment
Serial Year :
Link To Document :