2011
DOI: 10.1016/j.biortech.2010.08.039
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High-rate nitrogen removal by the Anammox process at ambient temperature

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Cited by 28 publications
(8 citation statements)
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“…(1) high-quality sludge retention can provide sufficient biomass accumulation (Van Hulle et al 2010;Vazquez-Padin et al 2010b), (2) microbial communities should be aggregated as granular sludge or biofilms to avoid the negative impact factor such as DO, and (3) anammox bacteria should be kept away from substrate inhibition, especially nitrite (Lotti et al 2012;Tang et al 2011;Yang et al 2011). Compared to flocculent biomass, biofilm is much more resistant to nitrite (Fernández et al 2012).…”
Section: Introductionmentioning
confidence: 99%
“…(1) high-quality sludge retention can provide sufficient biomass accumulation (Van Hulle et al 2010;Vazquez-Padin et al 2010b), (2) microbial communities should be aggregated as granular sludge or biofilms to avoid the negative impact factor such as DO, and (3) anammox bacteria should be kept away from substrate inhibition, especially nitrite (Lotti et al 2012;Tang et al 2011;Yang et al 2011). Compared to flocculent biomass, biofilm is much more resistant to nitrite (Fernández et al 2012).…”
Section: Introductionmentioning
confidence: 99%
“…Studies have shown that when the HCO 3 − concentration increased from 150 mg L −1 to 1500 mg L −1 , the TN removal efficiency increased to twice the initial value, 34 and the highest TN removal rate was 66.4 g N (m 3 d) −1 . 35 After the HCO 3 − concentration was further increased to 2000 mg L −1 , the TN removal rate dropped to 50% within 5 d, and the effluent TN concentration increased to 650 mg L −1 , which was lower than the inhibition level (75%) in other studies.…”
Section: Resultsmentioning
confidence: 99%
“…PCR-DGGE uses a GC-clamp primer (GC-clamp added to the 5´terminus of the forward primer) for amplification prior to gel electrophoresis. DGGE was used in previous studies of anammox samples (i) to detect key microorganisms that contributed to the loss of ammonium and nitrite in batch assay [64], (ii) to analyse bacterial population in the biofilm of the UASB reactor [39] and (iii) to study the microbial population in the anammox reactor [65]. DGGE has been commonly chosen to define phylogenetic relationships among bacteria because the technique can supply precise and abundant information concerning genetic diversity by separating different base-pair sequences (approximately 200-700 base pairs) [66].…”
Section: Denaturing Gradient Gel Electrophoresis (Dgge)mentioning
confidence: 99%