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Optimization of nitrogen removal from piggery waste by nitrite nitrification.

The piggery waste characteristics greatly vary with types of manure collections and the amount of water used. If solids are separated well, the waste strength will be greatly reduced resulting in lower TCOD/TKN ratio of 4 (average). If solids are separated by a mechanical scraper, some solids will remain and the waste strength will be increased with a TCOD/TKN ratio of 7. This study was conducted to find an optimum operating condition for nitrogen removal with these two ratios. Nitrite nitrification was targeted because it could be a short cut process for savings in oxygen for nitrification and carbon requirements for denitrification. The study results indicated that nitrogen loading rate and pH were the most important factors to be considered for stable nitrite nitrification. The applicable nitrogen loads were estimated to be 0.3 to 2.0 kgTKN/oxic m3/d for high TCOD/TKN ratio without pH control. With higher pH > 8, NO2N/NOxN ratios in oxic stages even with lower nitrogen loads were increased. The SBR with low TCOD/TKN ratio less than 4 required additional alkalinity. For a complete denitrification, the influent TCOD/TKN ratio must exceed 6 with oxic/total reactor volume ratio of 0.5. Nitrite nitrification and denitrification could save about 35% in tank volume and 50% in carbon requirement, respectively. However, 9.5% oxygen saving could be expected during the operation with low TCOD/TKN ratio. The elevated temperature due to the heat released from COD removal also enhanced microbial activities for nitrification and denitrification as well as ammonia stripping. However, careful attention must be provided for the reactor temperature not to inhibit the nitrification process.

Agriculture↗

The effect of C/N ratio on ammonia oxidising bacteria community structure in a laboratory nitrification-denitrification reactor.

A laboratory scale reactor operated as a single sludge, denitrification-nitrification bioreactor (DNB), was fed a synthetic wastewater. The effect of the C/N ratio of the influent on the structure of beta-proteobacterial autotrophic ammonia-oxidizing bacterial (AOB) communities was determined by DGGE analysis of 16S rRNA gene fragments amplified using a range of AOB-selective primers. Fluorescence in situ hybridisation (FISH) was used to determine quantitative changes in the AOB communities. When operated at a C/N ratio of 2 the DNB was effective in nitrogen removal and nitrification was measured at approximately 1.0 mg NH4+-N/g dry wt/h. Altering the C/N ratio to 5 resulted in a 50% reduction in nitrification rates. Nitrification was restored to its original level when the C/N ratio was returned to 2. AOB were detected by DGGE analysis of samples from the DNB under all operating conditions but the changes in C/N ratio and nitrification rates were accompanied by changes in the community structure of the AOB. However, quantitative FISH analysis indicated that beta-proteobacterial AOB were only present in high numbers (ca. 10(8) cells/ml) under the original operating conditions with a C/N ratio of 2. Beta-proteobacterial AOB could not be detected by FISH when the C/N ratio was 5. When nitrification activity was restored by returning the C/N ratio to 2, beta-proteobacterial AOB were still not detected and it is likely that either beta-proteobacterial AOB were not responsible for ammonia oxidation or that beta-proteobacterial AOB that did not contain the target sites for the range of 4 AOB selective probes used, were present in the reactor.

Ammonia↗

Nitrification-denitrification via nitrite for nitrogen removal from high nitrogen soybean wastewater with on-line fuzzy control.

This study is to demonstrate the performance of a new technology for complete nitrogen removal from soybean wastewater with high nitrogen concentrations. Nitrification-denitrification via nitrite was performed in three kinds of operating condition, i.e. nitrification-denitrification via nitrite under traditional SBR process, nitrification-denitrification via nitrite by alternating oxic/anoxic under fixed-time control and nitrification-denitrification via nitrite by alternating oxic/anoxic under on-line fuzzy control. The best one is nitrification-denitrification via nitrite by alternating oxic/anoxic under on-line fuzzy control. It not only improves both nitrification and denitrification rates and decreases total reaction time, but also saves the amount of added carbon source and alkalinity. In addition, reaction time can be shortened and operation cost can be saved by using real-time fuzzy control aeration and mixing time. So this method enhances the efficiency and the stability of nitrogen removal, and reduces operating costs and construction investment in the process of wastewater treatment.

Agriculture↗

High nitrification rate at low pH in a fluidized bed reactor with chalk as the biofilm carrier.

A typical steady state bulk pH of about 5 was established in a nitrifying fluidized bed with chalk as the only buffer agent. In spite of the low pH, high rate nitrification was observed with the nitrification kinetic parameters in the chalk reactor similar to those of biological reactors operating at pH>7. Various methods were used to determine the reasons for high rate nitrification at such low pH including (i) determination of bacterial species, (ii) microsensor measurements in the biofilm, and (iii) comparison of nitrification performance at low pH with a non-chalk fluidized bed reactor. Fluorescence in situ hybridization (FISH) using existing 16S rRNA-targeted oligonucleotide probes showed common nitrifying bacteria in the low pH chalk reactor. The prevalent nitrifying bacteria were identified in the Nitrosomonas oligotropha, Nitrosomonas europeae/eutropha, Nitrosospira and Nitrospira related groups, all well known nitrifiers. Microelectrode measurements showed that the pH in the biofilm was low and similar to that of the bulk pH. Finally, reactor performance using a non-chalk biofilm carrier (sintered glass) with the same bacterial inoculum also showed high rate nitrification below pH 5. The results suggest that inhibition of nitrification at low pH is highly overestimated.

Biofilms↗

[Potential of nitrification and denitrification in water purification system with hydroponic bio-filter method].

The potential of nitrification and denitrification of sediment and the density of ammonium-oxidizing bacteria and nitrite-oxidizing bacteria in sediment in water quality purifying system with hydroponic bio-filter method (HBFM) were measured. The variation of nitrification and denitrification potential of the sediment along the stream way was quantitatively studied. The results show that among the sediments from front, middle and retral part of the stream way, the sediment from middle part reached a maximum nitrification potential . nitrification potential of 4.76 x 10(-6) g/(g x h), while the sediment from front part reached a maximum denitrification potential of 8 .1 x 10(-7) g/(g x h). The distribution of nitrification potential accords with the ammonium-oxidizing bacteria density. The key for improving nitrogen removal efficiency of HBFM system consists in changing nitrification & denitrification region distributing and accordingly enhances denitrification process.

Biofilms↗

Boosting nitrification with the BABE technology.

Over the past years there has been a growing interest for compact, simple, low cost and robust technologies to upgrade wastewater treatment plants for nitrogen removal. The BABE (Bio Augmentation Batch Enhanced) technology is such a new concept. This patented system for biological treatment of sludge liquor - the effluent produced from digested sludge - uses a new principle, boosting the nitrifying bacteria in a side stream in such a way that the activated sludge in the main process is augmented. This augmentation increases the nitrification capacity of the wastewater treatment plant (wwtp). Experiments on a practical scale have demonstrated the effective and stable operation of the BABE technology. Model studies supported by the results of the full-scale tests showed that the technology can be applied in several situations, i.e. 1) introducing nitrification at high loaded wwtps; 2) enhancing nitrification at wwtps with incomplete nitrification; 3) enlarging denitrification at wwtps with complete nitrification. Most likely this year a full-scale application will be realized in the Netherlands at a wwtp with insufficient nitrification throughout the year.

Ammonia↗

Applicability of two-step models in estimating nitrification kinetics from batch respirograms under different relative dynamics of ammonia and nitrite oxidation.

A mechanistically based nitrification model was formulated to facilitate determination of both NH(4)(+)-N to NO(2)(-)-N and NO(2)(-)-N to NO(3)(-)-N oxidation kinetics from a single NH(4)(+)-N to NO(3)(-)-N batch-oxidation profile by explicitly considering the kinetics of each oxidation step. The developed model incorporated a novel convention for expressing the concentrations of nitrogen species in terms of their nitrogenous oxygen demand (NOD). Stoichiometric coefficients relating nitrogen removal, oxygen uptake, and biomass synthesis were derived from an electron-balanced equation.%A parameter identifiability analysis of the developed two-step model revealed a decrease in correlation and an increase in the precision of the kinetic parameter estimates when NO(2)(-)-N oxidation kinetics became increasingly rate-limiting. These findings demonstrate that two-step models describe nitrification kinetics adequately only when NH(4)(+)-N to NO(3)(-)-N oxidation profiles contain sufficient information pertaining to both nitrification steps. Thus, the rate-determining step in overall nitrification must be identified before applying conventionally used models to describe batch nitrification respirograms.

Ammonia↗

The effect of thiosulphate and other inhibitors of autotrophic nitrification on heterotrophic nitrifiers.

It has been found that heterotrophic nitrification by Thiosphaera pantotropha can be inhibited by thiosulphate in batch and chemostat cultures. Allythiourea and nitrapyrin, both classically considered to be specific inhibitors of autotrophic nitrification, inhibited nitrification by Tsa. pantotropha in short-term experiments with resting cell suspensions. Hydroxylamine inhibited ammonia oxidation in chemostat cultures, but was itself fully oxidized. Thus the total nitrification rate for the culture remained the same. Heterotrophic nitrification by another organism, a strain of "Pseudomonas denitrificans" has also been shown to be inhibited by thiosulphate in short term experiments and in the chemostat. During these experiments it became evident that this strain is able to grow mixotrophically (with acetate) and autotrophically in a chemostat with thiosulphate as the energy source.

Acetates↗

Stimulation of soil nitrification and denitrification by grazing in grasslands: do changes in plant species composition matter?

Stimulation of nitrification and denitrification by long term (from years to decades) grazing has commonly been reported in different grassland ecosystems. However, grazing generally induces important changes in plant species composition, and whether changes in nitrification and denitrification are primarily due to changes in vegetation composition has never been tested. We compared soil nitrification- and denitrification-enzyme activities (NEA and DEA, respectively) between semi-natural grassland sites experiencing intensive (IG) and light (LG) grazing/mowing regimes for 13 years. Mean NEA and DEA (i.e. observed from random soil sampling) were higher in IG than LG sites. The NEA/DEA ratio was higher in IG than LG sites, indicating a higher stimulation of nitrification. Marked changes in plant species composition were observed in response to the grazing/mowing regime. In particular, the specific phytomass volume of Elymus repens was lower in IG than LG sites, whereas the specific volume of Lolium perenne was higher in IG than LG sites. In contrast, the specific volume of Holcus lanatus, Poa trivialis and Arrhenatherum elatius were not significantly different between treatments. Soils sampled beneath grass tussocks of the last three species exhibited higher DEA, NEA and NEA/DEA ratio in IG than LG sites. For a given grazing regime, plant species did not affect significantly soil DEA, NEA and NEA/DEA ratio. The modification of plant species composition is thus not the primary factor driving changes in nitrification and denitrification in semi-natural grassland ecosystems experiencing long term intensive grazing. Factors such as trampling, N returned in animal excreta, and/or modification of N uptake and C exudation by frequently defoliated plants could be responsible for the enhanced microbial activities.

Animals↗

Nitrification and urea hydrolysis in deciduous woodland soils from a site exposed to heavy atmospheric pollution.

Laboratory studies of nitrification and urea hydrolysis were performed using soils obtained from sites exposed to pollution from a coking works and from a relatively unpolluted site. No net production of nitrate occurred in either soil when amended with ammonium sulphate alone, or together with CaCO(3) at 0.05% w/w. However, nitrate accumulated in both soils when 5% w/w CaCO(3) was added, with this amount of lime increasing the pH of both soils from around pH4 to pH7. Under these conditions, nitrification in the polluted soil occurred at about half the rate found in the relatively unpolluted soil. Urea hydrolysis occurred at a similar rate in both soils and was not impaired by exposure to coking pollution. Little nitrification of the ammonium liberated by urea hydrolysis occurred in either soil, however, presumably because, although the soil pH increased due to urea hydrolysis, it did not become sufficiently alkaline to support rapid nitrification. The relatively unpolluted soil used here was obtained from an area away from the coking works, but was exposed to generalised atmospheric pollution (wet and dry deposited acidity, greater than 1.0 and 2.4 kg H(+) ha(-1) yr(-1), respectively). Nitrification and urea hydrolysis occurred in these soils, so these processes were not inhibited by exposure to these relatively high background levels of air pollution.

Journal Article↗

An analysis of nitrification during the aerobic digestion of secondary sludges.

Investigations were undertaken to study the occurrence and progress of nitrification during aerobic digestion of activated sludge in a wide range of initial concentrations of total solids (1000 to 80 000 mg litre(-1), initial pH range of 4.5 to 10.4 and digestion temperature range of 5 degrees to 60 degrees C. Batch aerobic digestion studies on activated sludge grown on wastewater (enriched with organic solids from human excretal material) indicate that almost complete elimination of the 'biodegradable' matter of the activated sludge was one of the essential prerequisites to initiate nitrification. Favourable ranges of temperature and pH for nitrification were observed to be 25 degrees to 30 degrees C and 6.0 to 8.3, respectively. With all favourable conditions, a minimum period of about 2 days was necessary for population build-up of genera Nitrosomonas and Nitrobacter, and to initiate nitrification. Nitrate formation invariably lagged behind nitrite formation, but under certain conditions both phases of nitrification were observed to progress hand in hand.

Journal Article↗

Inhibition of nitrification in laboratory tests and model wastewater treatment plants.

The microbial elimination of nitrogen by combined nitrification and denitrification is a well-known technology in wastewater treatment processes. Nitrification in wastewater treatment plants is a sensitive microbiological process, which can be disturbed by toxic substances. Two laboratory methods for nitrification inhibition (ISO standard 9509 and a modification of the respiration inhibition test ISO 8192) were investigated with selected substances and compared with results from sewage model plants. For the prediction and prevention of interferences, the simple but reliable laboratory test methods proved to be very suitable. The tests in laboratory plants allowed a much more comprehensive evaluation of nitrification processes and showed their dependence on biodegradation and adaptation processes. The inhibition of nitrification depended on the mode of application and the biodegradability of the potential inhibitory compound and was much less severe with biodegradable substances than with poorly degradable ones.

Bacteria, Aerobic↗

Simultaneous assessment of nitrification and denitrification on freshwater epilithic biofilms by acetylene block method.

Acetylene (C2H2) inhibits key enzymes involved in nitrification (Ammonium monooxygenase) and denitrification (N2O reductases). Thus an injection of C2H2 at mid time of a batch type incubation make it possible to assess denitrification by measurement of the N2O accumulation as well as nitrification, calculated from the variations of the ammonium flux. As estimated by the "acetylene block technique", denitrification is known to be only a measure of the denitrification rate supported by nitrate diffusing from the water column (Dw). This paper presents a first application on river epilithic biofilms which proved that the simultaneous measurement of Dw and nitrification allows the estimation of the order of magnitude of total denitrification (Dt) when nitrification is detected in the tested sample. This approach appears to be an easy tool for determination of nitrification and denitrification in natural samples and as thus presents an alternative to isotopic 15N methods.

Acetylene↗

Nitrification efficiency and nitrifying bacteria abundance in combined AS-RBC and A2O systems.

This study makes a comparison between the nitrification performance of TNCU-I (a combined activated sludge-rotating biological contactor process) and A2O systems by the use of a pilot plant and batch experiments. The nitrifier abundance in both systems was determined, using cloning-denaturing gradient gel electrophoresis (DGGE) and fluorescent in-situ hybridization (FISH), to investigate the role of rotating biological contactor in the TNCU-I process. The stability of the nitrification performance and the specific nitrification rate were found to be greater in TNCU-I system than in the A2O system. RBC biofilm promoted nitrifying activity that contributed to the nitrification performance, especially at a low SRT. By using the cloning-DGGE method, the genera Nitrosospira and Nitrospira were found to be present in all the samples, while the genus Nitrosomonas was observed only in the TNCU-I RBC biofilm. In addition, the proportions of ammonia oxidizer in the TNCU-I RBC biofilm, the TNCU-I activated sludge and the A2O activated sludge were 11.4%, 13.2%, and 4.1%, respectively, higher than the nitrite oxidizer fractions of 3.3%, 5.7% and 2.1%, respectively, according to the cloning-DGGE method. On the other hand, the proportions of ammonia oxidizers in the afore-mention materials were 10.3%, 13.7%, and 5.2%, higher than the nitrite oxidizer fractions of 2.5%, 3.6% and 2.3%, according to the FISH experiments. This implies that the proportion of ammonia oxidizer in the TNCU-I process was 3.2 and 2.6 times that in the A2O process, determined by the cloning-DGGE and FISH methods, respectively. These amounts are also close to the ammonia oxidization rate of 2.9 times. All the data show that RBC added to the aerobic zone of TNCU-I process would increase the nitrifier abundance and enhance the nitrification performance of the system.

Bacteria, Aerobic↗

Kinetics of sequential nitrification and denitrification processes.

Kinetics of nitrification and denitrification of synthetic wastewater was investigated by using two reactors in series. An activated sludge unit was used for nitrification followed by a downflow biofilter for denitrification. Glucose solution was fed to the denitrification column to supply carbon source. Reactors were operated at different operating conditions and data were collected for determination of kinetic constants. Experimental data indicated that nitrification and denitrification kinetics followed Monod kinetics. By using the experimental data, kinetic constants for nitrification were determined as k = 1.15 d(-1), K(N) = 5.14 mg/l, Y = 0.34 mgX/mgN and b = -0.021 d(-1). Similarly, kinetic constants for denitrification were determined as k = 0.23 d(-1) and K(DN) = 0.27 mg/l. Rates of nitrification and denitrification increased with increasing nitrogen loading rate.

Journal Article↗

The influence of long emersion on biota, ammonium fluxes and nitrification in intertidal sediments of Marennes-Oléron Bay, France.

A comparative study between waterlogged and reflooded intertidal sediments was undertaken in March and June 1999 through statistical analysis of selected sediment parameters (biota, salinity, O2, Eh), pool sizes and benthic fluxes of nutrients (NH4+, NO2-, NO3-) and nitrification rates. In March samples, absence of polychaetes and oligochaetes from upper sediment horizons were due to erosional events sweeping away surface sediments. Presence of richer annelid assemblages in June samples indicated more stable hydrodynamic conditions that favoured the development of benthic microalgae biofilms. Dewatering of sediments during a 3-day emersion period promoted a salinity rise on top layers, migration of pore water ions towards the sediment surface, and created sediment fissures that accelerated water exchange on reflooding. Reflooded and waterlogged sediment systems were comparable with respect to the release of NH4+ to overlying water but were different with respect to nitrification rates. Sediment-water NH4+ fluxes were higher (P = 0.011) in March (3.3 mmol m(-2) day(-1) compared to June (1.4 mmol m(-2) day(-1) due to higher macrofauna biomasses and lower benthic microalgae concentrations in March samples. Potential nitrification rates (range from 19 to 60 mmol NO3- (-2) day(-1)) were not statistically different between March and June. A thinner oxic layer in reflooded compared with waterlogged systems reflects a decrease of O2 diffusion into sediment at high salinities which resulted in the fall of the actual nitrification rates (P < 0.05). Our data suggest that long term dessication of intertidal sediments may depress the nitrification process at the ecosystem level.

Analysis of Variance↗

Simultaneous nitrification and denitrification using an autotrophic membrane-immobilized biofilm reactor.

AIMS: To develop a laboratory-scale autotrophic membrane-immobilized biofilm reactor to remove nitrogen from drinking water. METHODS AND RESULTS: A polyvinyl alcohol (PVA) immobilized biofilm, attached to the surface of a silicone tube, was used as the basis of a bioreactor for simultaneous nitrification and denitrification of water. The bioreactor was aerated with air to supply oxygen for nitrification. Pure hydrogen was supplied to the silicone tube and diffused through the membrane wall to feed the biofilm for autotrophic denitrification. The bioreactor was effective for the simultaneous nitrification and denitrification of water after a short period of acclimation, while the biofilm exhibited good resistance to the inhibition of denitrification by dissolved oxygen; the denitrification rate decreased by only 8% as the dissolved oxygen increased from 2 mg l(-1) to saturation. CONCLUSIONS: By using PVA crosslinked with sodium nitrate to entrap nitrifying and denitrifying sludge on the surface of a silicone tube, a novel bioreactor for simultaneous nitrification and denitrification was developed. In addition to performing as an immobilizing agent to strengthen the biofilm, PVA protected the denitrifying microorganisms to reduce the inhibition by dissolved oxygen under aerobic condition. Therefore, nitrification and denitrification occurred simultaneously within the biofilm. Furthermore, the immobilization technique shortened the acclimation period of the bioreactor. SIGNIFICANCE AND IMPACT OF THE STUDY: The described space saving and simple to operate bioreactor for nitrogen removal performed autotrophic denitrification to solve the problem of residual carbon in heterotrophic denitrification, and thus is suitable for removing nitrogen from drinking water.

Ammonia↗

Impact of backwashing on nitrification in the biological activated carbon filters used in drinking water treatment.

Nitrification during biological filtration is currently used in drinking water production to remove ammonia, which is the source of several water quality problems during treatment and distribution. We evaluated here the impact of backwashing on nitrification efficiency in filters used for drinking water treatment. Two different granular activated carbon (one open and one closed carbon superstructure) were tested. Ammonia removal and fixed nitrifying bacterial biomass before and after backwashing were compared in first-stage pilot filters and full-scale second-stage filters. Backwashing has a greater impact on nitrification on first-stage than an second-stage filters. Backwashing improved the ammonia removal in warm (> or = 18 degrees C) water in a first-stage filter containing an open-superstructure granular activated carbon, whereas a closed-superstructure support showed a removal capacity that is less after a regular backwashing than before, or similar to it. In cold water (< or = 4 degrees C), backwashing had a negative impact on nitrification capacity in an open-superstructure medium first-stage filter. In full-scale second-stage filters, backwashing had a slight negative impact on filter performances for both open- and closed-superstructure media at temperatures between 8 degrees C and 12 degrees C. In colder waters (< or = 3 degrees C), nitrification was very poor both before and after backwashing. Sampling of fixed, nitrifying biomass in the pilot filter columns showed that in all cases (low and high expansion backwash; both media tested) and at 20 +/- 3 degrees C the overall biomass levels remained unchanged before and after backwash. In the full-scale second-stage filters, nitrifying bionass was similar before and after backwashing for both types of media tested.

Ammonia↗