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Microbial processes and bacterial populations associated to anaerobic treatment of sulfate-rich wastewater
A pilot-scale (1.2 m 3) anaerobic sequencing batch biofilm reactor (ASBBR) containing mineral coal for biomass attachment was fed with sulfate-rich wastewater at increasing sulfate concentrations. Ethanol was used as the main organic source. Tested COD/sulfate ratios were of 1.8 and 1.5 for sulfate...
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Published in: | Process biochemistry (1991) 2010-02, Vol.45 (2), p.164-170 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A pilot-scale (1.2
m
3) anaerobic sequencing batch biofilm reactor (ASBBR) containing mineral coal for biomass attachment was fed with sulfate-rich wastewater at increasing sulfate concentrations. Ethanol was used as the main organic source. Tested COD/sulfate ratios were of 1.8 and 1.5 for sulfate loading rates of 0.65–1.90
kgSO
4
2−/cycle (48
h-cycle) or of 1.0 in the trial with 3.0
gSO
4
2−
l
−1. Sulfate removal efficiencies observed in all trials were as high as 99%. Molecular inventories indicated a shift on the microbial composition and a decrease on species diversity with the increase of sulfate concentration.
Beta-proteobacteria species affiliated with
Aminomonas spp. and
Thermanaerovibrio spp. predominated at 1.0
gSO
4
2−
l
−1. At higher sulfate concentrations the predominant bacterial group was
Delta-proteobacteria mainly
Desulfovibrio spp. and
Desulfomicrobium spp. at 2.0
gSO
4
2−
l
−1, whereas
Desulfurella spp. and
Coprothermobacter spp. predominated at 3.0
gSO
4
2−
l
−1. These organisms have been commonly associated with sulfate reduction producing acetate, sulfide and sulfur. Methanogenic archaea (
Methanosaeta spp.) was found at 1.0 and 2.0
gSO
4
2−
l
−1. Additionally, a simplified mathematical model was used to infer on metabolic pathways of the biomass involved in sulfate reduction. |
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ISSN: | 1359-5113 1873-3298 |
DOI: | 10.1016/j.procbio.2009.09.002 |