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Biocorrosion and biofilm formation in a nutrient limited heating system subjected to alternating microaerophilic conditions
Authors:B. B. Kjellerup  K. U. Kjeldsen  F. Lopes  L. Abildgaard  K. Ingvorsen  B. Frølund
Affiliation:1. Department of Biotechnology, Chemistry and Environmental Engineering , Aalborg University , Sohngaardsholmsvej 49, DK-9000 Aalborg, Denmark;2. Center of Marine Biotechnology, University of Maryland Biotechnology Institute , 701 E. Pratt St, Baltimore , MD , 21202 , USA kjellerup@comb.umbi.umd.edu;4. Department of Biological Sciences, Section for Microbiology , Aarhus University , Ny Munkegade, Building 1540, DK-8000, ?rhus C., Denmark;5. Department of Biological Engineering , University of Minho , Campus de Gualtar, 4710–057 Braga, Portugal;6. Danish Technological Institute, Centre for Chemical and Water Technology , Teknologiparken, DK-8000 ?rhus C., Denmark
Abstract:Severe biofilm formation and biocorrosion have been observed in heating systems even when the water quality complied with existing standards. The coupling between water chemistry, biofilm formation, species composition, and biocorrosion in a heating system was investigated by adding low concentrations of nutrients and oxygen under continuous and alternating dosing regimes. Molecular analysis of 16S rRNA gene fragments demonstrated that the amendments did not cause changes in the overall bacterial community composition. The combined alternating dosing of nutrients and oxygen caused increased rates of pitting (bio-) corrosion. Detection of bacteria involved in sulfide production and oxidation by retrieval of the functional dsrAB and apsA genes revealed the presence of Gram-positive sulfate- and sulfite-reducers and an unknown sulfur-oxidizer. Therefore, to control biocorrosion, sources of oxygen and nutrients must be limited, since the effect of the alternating operational conditions apparently is more important than the presence of potentially corrosive biofilm bacteria.
Keywords:biocorrosion  biofilm  heating systems  sulfate reducing bacteria (SRB)  functional genes dsrAB and apsA
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