Microbial characterization and degradation of linear alkylbenzene sulfonate in an anaerobic reactor treating wastewater containing soap powder

•The anaerobic degradation of liner alkylbenzene sulfonate (LAS) was evaluated.•The fluidized bed reactor was operated with a hydraulic retention time of 15h.•LAS degradation was 48% and the VFA increased with its addition.•Dechloromonas sp. and Geobacter sp. were identified in LAS degradation.•The...

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Published inBioresource technology Vol. 167; pp. 316 - 323
Main Authors Carosia, Mariana Fronja, Okada, Dagoberto Yukio, Sakamoto, Isabel Kimiko, Silva, Edson Luiz, Varesche, Maria Bernadete Amâncio
Format Journal Article
LanguageEnglish
Published Kidlington Elsevier Ltd 01.09.2014
Elsevier
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Summary:•The anaerobic degradation of liner alkylbenzene sulfonate (LAS) was evaluated.•The fluidized bed reactor was operated with a hydraulic retention time of 15h.•LAS degradation was 48% and the VFA increased with its addition.•Dechloromonas sp. and Geobacter sp. were identified in LAS degradation.•The compounds of soap powder affected the LAS removal and volatile fatty acids. The aim of this study was to evaluate the removal of linear alkylbenzene sulfonate (LAS) in an anaerobic fluidized bed reactor (AFBR) treating wastewater containing soap powder as LAS source. At Stage I, the AFBR was fed with a synthetic substrate containing yeast extract and ethanol as carbon sources, and without LAS; at Stage II, soap powder was added to this synthetic substrate obtaining an LAS concentration of 14±3mgL−1. The compounds of soap powder probably inhibited some groups of microorganisms, increasing the concentration of volatile fatty acids (VFA) from 91 to 143mgHAcL−1. Consequently, the LAS removal rate was 48±10% after the 156days of operation. By sequencing, 16S rRNA clones belonging to the phyla Proteobacteria and Synergistetes were identified in the samples taken at the end of the experiment, with a remarkable presence of Dechloromonas sp. and Geobacter sp.
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ISSN:0960-8524
1873-2976
DOI:10.1016/j.biortech.2014.06.002