Selective Inhibition of Nitrite Oxidation by Methanoic Acid Dosing in Sequencing Batch Reactor

2017 ◽  
Vol 34 (2) ◽  
pp. 73-79
Author(s):  
Na Li ◽  
Xiaomin Hu ◽  
Guode Li
2004 ◽  
Vol 49 (5-6) ◽  
pp. 47-55 ◽  
Author(s):  
C.S. Gee ◽  
J.S. Kim

Biological ammonia-nitrogen removal utilizes two distinct processes, nitrification and denitrification. In nitrification, ammonia oxidizes to nitrite then to nitrate. In this study, elimination of nitrite oxidation to nitrate step was attempted in order to directly remove nitrite to nitrogen gas by denitrification. For this study the supernatant from an anaerobic digester was used as an ammonia source and a sequencing batch reactor (SBR) was employed. Emphasis was given to the evaluation of the operational factors affecting nitrite accumulation and the elucidation of kinetics for biological nitrification and denitrification. Accumulation of nitrite in the nitrification process was achieved by suppressing the growth of Nitrobacter, a nitrite oxidizer, by loading high concentration ammonia supernatant immediately after all ammonia in the previous loading was oxidized to nitrite. Nitrite oxidation was taking place as the solid retention time (SRT) was increased from 2.5 days to 3.0 days in a continuously aerated SBR mode with daily feeding. However, nitrite accumulation was achieved even at longer SRT of 5 days when the aeration and non-aeration periods were appropriately combined and the non-aeration period can be used for denitrification of the accumulated nitrite with a carbon source supplied.


2015 ◽  
Vol 73 (5) ◽  
pp. 1067-1073 ◽  
Author(s):  
Xinyu Wan ◽  
Pengying Xiao ◽  
Daijun Zhang ◽  
Peili Lu ◽  
Zongbao Yao ◽  
...  

The kinetics for ammonium (NH4+) oxidation and nitrite (NO2−) oxidation under the effect of hydroxylamine (NH2OH) were studied by respirometry using the nitrifying sludge from a laboratory-scale sequencing batch reactor. Modified models were used to estimate kinetics parameters of ammonia and nitrite oxidation under the effect of hydroxylamine. An inhibition effect of hydroxylamine on the ammonia oxidation was observed under different hydroxylamine concentration levels. The self-inhibition coefficient of hydroxylamine oxidation and noncompetitive inhibition coefficient of hydroxylamine for nitrite oxidation was estimated by simulating exogenous oxygen-uptake rate profiles, respectively. The inhibitive effect of NH2OH on nitrite-oxidizing bacteria was stronger than on ammonia-oxidizing bacteria. This work could provide fundamental data for the kinetic investigation of the nitrification process.


2019 ◽  
Vol 1 (2) ◽  
pp. 1
Author(s):  
Lindawati Lindawati

Sebuah Sequencing Batch Reactor (SBR) digunakan untuk mengevaluasi peranan Biochemical Oxygen Demand (BOD) biosensor dalam proses optimasi proses pengolahan nutrien karbon, nitrogen dan fosfat. Hasil penelitian menunjukkan bahwa BOD biosensor dapat dipergunakan untuk penentuan karbon organik, sehingga reduksi siklus SBR dapat dilakukan dan efisiensi proses meningkat. Pola konsumsi karbon organik ditemukan dengan adanya ‘tanda diam’ pada fase anoksik/ anaerobik, di mana dari tanda ini, fase aerobik dapat segera dimulai. Reduksi durasi siklus SBR dari 8 jam menjadi 4 jam meningkatkan efiesiensi pengolahan C, N dan P yang meningkat pula (hampir dua kali lebih tinggi).


1994 ◽  
Vol 30 (6) ◽  
pp. 237-246 ◽  
Author(s):  
A. Carucci ◽  
M. Majone ◽  
R. Ramadori ◽  
S. Rossetti

This paper describes a lab-scale experimentation carried out to study enhanced biological phosphate removal (EBPR) in a sequencing batch reactor (SBR). The synthetic feed used was based on peptone and glucose as organic substrate to simulate the readily biodegradable fraction of a municipal wastewater (Wentzel et al., 1991). The experimental work was divided into two runs, each characterized by different operating conditions. The phosphorus removal efficiency was considerably higher in the absence of competition for organic substrate between P-accumulating and denitrifying bacteria. The activated sludge consisted mainly of peculiar microorganisms recently described by Cech and Hartman (1990) and called “G bacteria”. The results obtained seem to be inconsistent with the general assumption that the G bacteria are characterized by anaerobic substrate uptake not connected with any polyphosphate metabolism. Supplementary anaerobic batch tests utilizing glucose, peptone and acetate as organic substrates show that the role of acetate in the biochemical mechanisms promoting EBPR may not be so essential as it has been assumed till now.


1992 ◽  
Vol 26 (9-11) ◽  
pp. 2049-2052 ◽  
Author(s):  
G. Buitrón ◽  
A. Koefoed ◽  
B. Capdeville

The microbial activity during the aerobic acclimation of activated sludge to phenol was studied. Carbon dioxide evolution rate (CER), measured in a sequencing batch reactor coupled to an infra-red system, was utilized as the activity control parameter. It was found that CER is representative of the microbial metabolism. Moreover, it was observed that starvation periods during acclimation had a negative effect on biodegradation rate.


1996 ◽  
Vol 34 (3-4) ◽  
pp. 413-420
Author(s):  
Y. C. Liao ◽  
D. J. Lee

Transient model of oxygen transfer rate in a sequencing batch reactor is derived and solved numerically. The dissolved oxygen response under several conditions is analyzed. Effects of operational parameters and liquid bath height are studied. When with short, intermittent aeration periods, the transient effects on oxygen transfer rate may be substantial and should be taken into considerations. An example considering bioreaction is also given.


1998 ◽  
Vol 37 (4-5) ◽  
pp. 95-98 ◽  
Author(s):  
Nancy G. Love ◽  
Mary E. Rust ◽  
Kathy C. Terlesky

An anaerobic enrichment culture was developed from an anoxic/anaerobic/aerobic activated sludge sequencing batch reactor using methyl ethyl ketoxime (MEKO), a potent nitrification inhibitor, as the sole carbon and energy source in the absence of molecular oxygen and nitrate. The enrichment culture was gradually fed decreasing amounts of biogenic organic compounds and increasing concentrations of MEKO over 23 days until the cultures metabolized the oxime as the sole carbon source; the cultures were maintained for an additional 41 days on MEKO alone. Turbidity stabilized at approximately 100 mg/l total suspended solids. Growth on selective media plates confirmed that the microorganisms were utilizing the MEKO as the sole carbon and energy source. The time frame required for growth indicated that the kinetics for MEKO degradation are slow. A batch test indicated that dissolved organic carbon decreased at a rate comparable to MEKO consumption, while sulfate was not consumed. The nature of the electron acceptor in anaerobic MEKO metabolism is unclear, but it is hypothesized that the MEKO is hydrolyzed intracellularly to form methyl ethyl ketone and hydroxylamine which serve as electron donor and electron acceptor, respectively.


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