Autotrophic nitrogen removal from black water: Calcium addition as a requirement for settleability

Black (toilet) water contains half of the organic load in the domestic wastewater, as well as the major fraction of the nutrients nitrogen and phosphorus. When collected with vacuum toilets, the black water is 25 times more concentrated than the total domestic wastewater stream, i.e. including grey water produced by laundry, showers etc. A two-stage nitritation-anammox process was successfully employed and removed 85%-89% of total nitrogen in anaerobically treated black water. The (free) calcium concentration in black water was too low (42 mg/L) to obtain sufficient granulation of anammox biomass. The granulation and retention of the biomass was improved considerably by the addition of 39 mg/L of extra calcium. This resulted in a volumetric nitrogen removal rate of 0.5 gN/L/d, irrespective of the two temperatures of 35 °C and 25 °C at which the anammox reactors were operated. Nitrous oxide, a very strong global warming gas, was produced in situations of an incomplete anammox conversion accompanied by elevated levels of nitrite.     

Integration of anammox into the aerobic granular sludge process for main stream wastewater treatment at ambient temperatures

Anaerobic ammonium oxidation, nitrification and removal of COD was studied at ambient temperature (18 °C ± 3) in an anoxic/aerobic granular sludge reactor during 390 days. The reactor was operated in a sequencing fed batch mode and was fed with acetate and ammonium containing medium with a COD/N ratio of 0.5 [g COD/gN]. During influent addition, the medium was mixed with recycled effluent which contained nitrate in order to allow acetate oxidation and nitrate reduction by anammox bacteria. In the remainder of the operational cycle the reactor was aerated and controlled at a dissolved oxygen concentration of 1.5 mg O₂/l in order to establish simultaneous nitritation and Anammox. Fluorescent in-situ hybridization (FISH) revealed that the dominant Anammox bacterial population shifted toward Candidatus “Brocadia fulgida” which is known to be capable of organotrophic nitrate reduction. The reactor achieved stable volumetric removal rates of 900 [g N₂-N/m³/day] and 600 [g COD/m³/day]. During the total experimental period Anammox bacteria remained dominant and the sludge production was 5 fold lower than what was expected by heterotrophic growth suggesting that consumed acetate was not used by heterotrophs. These observations show that Anammox bacteria can effectively compete for COD at ambient temperatures and can remove effectively nitrate with a limited amount of acetate. This study indicates a potential successful route toward application of Anammox in granular sludge reactors on municipal wastewater with a limited amount of COD.     

Treating landfill leachate using passive aeration trickling filters; effects of leachate characteristics and temperature on rates and process dynamics

Biological ammoniacal-nitrogen (NH₄⁺-N) and organic carbon (TOC) treatment was investigated in replicated mesoscale attached microbial film trickling filters, treating strong and weak strength landfill leachates in batch mode at temperatures of 3, 10, 15 and 30 °C. Comparing leachates, rates of NH₄⁺-N reduction (0.126-0.159 g m^− 2 d^− 1) were predominantly unaffected by leachate characteristics; there were significant differences in TOC rates (0.072-0.194 g m^− 2 d^− 1) but no trend relating to leachate strength. Rates of total oxidised nitrogen (TON) accumulation (0.012-0.144 g m^− 2 d^− 1) were slower for strong leachates. Comparing temperatures, treatment rates varied between 0.029-0.319 g NH₄⁺-N m^− 2 d^− 1 and 0.033-0.251 g C m^− 2 d^− 1 generally increasing with rising temperatures; rates at 3 °C were 9 and 13% of those at 30 °C for NH₄⁺-N and TOC respectively. For the weak leachates (NH₄⁺-N < 140 mg l^− 1) complete oxidation of NH₄⁺-N was achieved. For the strong leachates (NH₄⁺-N 883-1150 mg l^− 1) a biphasic treatment response resulted in NH₄⁺-N removal efficiencies of between 68 and 88% and for one leachate no direct transformation of NH₄⁺-N to TON in bulk leachate. The temporal decoupling of NH₄⁺-N oxidation and TON accumulation in this leachate could not be fully explained by denitrification, volatilisation or anammox, suggesting temporary storage of N within the treatment system. This study demonstrates that passive aeration trickling filters can treat well-buffered high NH₄⁺-N strength landfill leachates under a range of temperatures and that leachate strength has no effect on initial NH₄⁺-N treatment rates. Whether this approach is a practicable option depends on a range of site specific factors.     

Interaction between temperature and ammonia in mesophilic digesters for animal waste treatment

Four anaerobic sequencing batch reactors (ASBRs) were operated during a period of 988 days to evaluate the effect of temperature, ammonia, and their interconnectivity on the methane yield of anaerobic processes for animal waste treatment. During period 1 (day 0-378), the methane yield was 0.31 L CH₄/g volatile solids (VS) for all digesters (with no statistical differences among them) at a temperature and total ammonium-N levels of 25 °C and ∼1200 mg NH₄⁺-N/L, respectively. During period 2 (day 379-745), the methane yield at 25 °C decreased by 45% when total ammonium-N and ammonia-N were increased in two of the four ASBRs to levels >4000 mg NH₄⁺-N/L and >80 mg NH₃-N/L, respectively. During period 3 (day 746-988), this relative inhibition was reduced from 45% to 13% compared to the low-ammonia control reactors when the operating temperature was increased from 25 °C to 35 °C (while the free ammonia levels increased from ∼100 to ∼250 mg NH₃-N/L). The 10 °C increase in temperature doubled the rate constant for methanogenesis, which overwhelmed the elevated toxicity effects caused by the increasing concentration of free ammonia. Thus, the farmer/operator may alleviate ammonia toxicity by increasing the operating temperature within the mesophilic range. We extrapolated our data to correlate temperature, ammonia, and methane yield and to hypothesize that the difference between high- and low-ammonia reactors is negligible at the optimum mesophilic temperature of 38 °C.     

Simultaneous heterotrophic and sulfur-oxidizing autotrophic denitrification process for drinking water treatment: control of sulfate production

A long-term performance of a packed-bed bioreactor containing sulfur and limestone was evaluated for the denitrification of drinking water. Autotrophic denitrification rate was limited by the slow dissolution rate of sulfur and limestone. Dissolution of limestone for alkalinity supplementation increased hardness due to release of Ca²⁺. Sulfate production is the main disadvantage of the sulfur autotrophic denitrification process. The effluent sulfate concentration was reduced to values below drinking water guidelines by stimulating the simultaneous heterotrophic and autotrophic denitrification with methanol supplementation. Complete removal of 75 mg/L NO₃-N with effluent sulfate concentration of around 225 mg/L was achieved when methanol was supplemented at methanol/NO₃-N ratio of 1.67 (mg/mg), which was much lower than the theoretical value of 2.47 for heterotrophic denitrification. Batch studies showed that sulfur-based autotrophic NO₂-N reduction rate was around three times lower than the reduction rate of NO₃-N, which led to NO₂-N accumulation at high loadings.     

Floc-based sequential partial nitritation and anammox at full scale with contrasting N2O emissions

New Activated Sludge (NAS^®) is a hybrid, floc-based nitrogen removal process without carbon addition, based on the control of sludge retention times (SRT) and dissolved oxygen (DO) levels. The aim of this study was to examine the performance of a retrofitted four-stage NAS^® plant, including on-line measurements of greenhouse gas emissions (N₂O and CH₄). The plant treated anaerobically digested industrial wastewater, containing 264 mg N L⁻¹, 1154 mg chemical oxygen demand (COD) L⁻¹ and an inorganic carbon alkalinity of 34 meq L⁻¹. The batch-fed partial nitritation step received an overall nitrogen loading rate of 0.18-0.22 kg N m⁻³ d⁻¹, thereby oxidized nitrogen to nitrite (45-47%) and some nitrate (13-15%), but also to N₂O (5.1-6.6%). This was achieved at a SRT of 1.7 d and DO around 1.0 mg O₂ L⁻¹. Subsequently, anammox, denitrification and nitrification compartments were followed by a final settler, at an overall SRT of 46 d. None of the latter three reactors emitted N₂O. In the anammox step, 0.26 kg N m⁻³ d⁻¹ was removed, with an estimated contribution of 71% by the genus Kuenenia, which constituted 3.1% of the biomass. Overall, a nitrogen removal efficiency of 95% was obtained, yielding a dischargeable effluent. Retrofitting floc-based nitrification/denitrification with carbon addition to NAS^® allowed to save 40% of the operational wastewater treatment costs. Yet, a decrease of the N₂O emissions by about 50% is necessary in order to obtain a CO₂ neutral footprint. The impact of emitted CH₄ was 20 times lower.     

Ammonium adsorption in aerobic granular sludge, activated sludge and anammox granules

The ammonium adsorption properties of aerobic granular sludge, activated sludge and anammox granules have been investigated. During operation of a pilot-scale aerobic granular sludge reactor, a positive relation between the influent ammonium concentration and the ammonium adsorbed was observed. Aerobic granular sludge exhibited much higher adsorption capacity compared to activated sludge and anammox granules. At an equilibrium ammonium concentration of 30 mg N/L, adsorption obtained with activated sludge and anammox granules was around 0.2 mg NH₄-N/g VSS, while aerobic granular sludge from lab- and pilot-scale exhibited an adsorption of 1.7 and 0.9 mg NH₄-N/g VSS, respectively. No difference in the ammonium adsorption was observed in lab-scale reactors operated at different temperatures (20 and 30 °C). In a lab-scale reactor fed with saline wastewater, we observed that the amount of ammonium adsorbed considerably decreased when the salt concentration increased. The results indicate that adsorption or better ion exchange of ammonium should be incorporated into models for nitrification/denitrification, certainly when aerobic granular sludge is used.     

Characterization of effluent water qualities from satellite membrane bioreactor facilities

Membrane bioreactors (MBRs) are often a preferred treatment technology for satellite water recycling facilities since they produce consistent effluent water quality with a small footprint and require little or no supervision. While the water quality produced from centralized MBRs has been widely reported, there is no study in the literature addressing the effluent quality from a broad range of satellite facilities. Thus, a study was conducted to characterize effluent water qualities produced by satellite MBRs with respect to organic, inorganic, physical and microbial parameters. Results from sampling 38 satellite MBR facilities across the U.S. demonstrated that 90% of these facilities produced nitrified (NH₄-N <0.4 mg/L-N) effluents that have low organic carbon (TOC <8.1 mg/L), turbidities of <0.7 NTU, total coliform bacterial concentrations <100 CFU/100 mL and indigenous MS-2 bacteriophage concentrations <21 PFU/100 mL. Multiple sampling events from selected satellite facilities demonstrated process capability to consistently produce effluent with low concentrations of ammonia, TOC and turbidity. UV-254 transmittance values varied substantially during multiple sampling events indicating a need for attention in designing downstream UV disinfection systems. Although enteroviruses, rotaviruses and hepatitis A viruses (HAV) were absent in all samples, adenoviruses were detected in effluents of all nine MBR facilities sampled. The presence of Giardia cysts in filtrate samples of two of nine MBR facilities sampled demonstrated the need for an appropriate disinfection process at these facilities.     

N2O emission from a partial nitrification-anammox process and identification of a key biological process of N2O emission from anammox granules

Emission of nitrous oxide (N₂O) during biological wastewater treatment is of growing concern. The emission of N₂O from a lab-scale two-reactor partial nitrification (PN)-anammox reactor was therefore determined in this study. The average emission of N₂O from the PN and anammox process was 4.0 ± 1.5% (9.6 ± 3.2% of the removed nitrogen) and 0.1 ± 0.07% (0.14 ± 0.09% of the removed nitrogen) of the incoming nitrogen load, respectively. Thus, a larger part (97.5%) of N₂O was emitted from the PN reactor. The total amount of N₂O emission from the PN reactor was correlated to nitrite (NO₂⁻) concentration in the PN effluent rather than DO concentration. In addition, further studies were performed to indentify a key biological process that is responsible for N₂O emission from the anammox process (i.e., granules). In order to characterize N₂O emission from the anammox granules, the in situ N₂O production rate was determined by using microelectrodes for the first time, which was related to the spatial organization of microbial community of the granule as determined by fluorescence in situ hybridization (FISH). Microelectrode measurement revealed that the active N₂O production zone was located in the inner part of the anammox granule, whereas the active ammonium consumption zone was located above the N₂O production zone. Anammox bacteria were present throughout the granule, whereas ammonium-oxidizing bacteria (AOB) were restricted to only the granule surface. In addition, addition of penicillin G that inhibits most of the heterotrophic denitrifiers and AOB completely inhibited N₂O production in batch experiments. Based on these results obtained, denitrification by putative heterotrophic denitrifiers present in the inner part of the granule was considered the most probable cause of N₂O emission from the anammox reactor (i.e., granules).     

Nitrate removal, communities of denitrifiers and adverse effects in different carbon substrates for use in denitrification beds

Denitrification beds are containers filled with wood by-products that serve as a carbon and energy source to denitrifiers, which reduce nitrate (NO₃⁻) from point source discharges into non-reactive dinitrogen (N₂) gas. This study investigates a range of alternative carbon sources and determines rates, mechanisms and factors controlling NO₃⁻ removal, denitrifying bacterial community, and the adverse effects of these substrates. Experimental barrels (0.2 m³) filled with either maize cobs, wheat straw, green waste, sawdust, pine woodchips or eucalyptus woodchips were incubated at 16.8 °C or 27.1 °C (outlet temperature), and received NO₃⁻ enriched water (14.38 mg N L⁻¹ and 17.15 mg N L⁻¹). After 2.5 years of incubation measurements were made of NO₃⁻-N removal rates, in vitro denitrification rates (DR), factors limiting denitrification (carbon and nitrate availability, dissolved oxygen, temperature, pH, and concentrations of NO₃⁻, nitrite and ammonia), copy number of nitrite reductase (nirS and nirK) and nitrous oxide reductase (nosZ) genes, and greenhouse gas production (dissolved nitrous oxide (N₂O) and methane), and carbon (TOC) loss. Microbial denitrification was the main mechanism for NO₃⁻-N removal. Nitrate-N removal rates ranged from 1.3 (pine woodchips) to 6.2 g N m⁻³ d⁻¹ (maize cobs), and were predominantly limited by C availability and temperature (Q₁₀ = 1.2) when NO₃⁻-N outlet concentrations remained above 1 mg L⁻¹. The NO₃⁻-N removal rate did not depend directly on substrate type, but on the quantity of microbially available carbon, which differed between carbon sources. The abundance of denitrifying genes (nirS, nirK and nosZ) was similar in replicate barrels under cold incubation, but varied substantially under warm incubation, and between substrates. Warm incubation enhanced growth of nirS containing bacteria and bacteria that lacked the nosZ gene, potentially explaining the greater N₂O emission in warmer environments. Maize cob substrate had the highest NO₃⁻-N removal rate, but adverse effects include TOC release, dissolved N₂O release and substantial carbon consumption by non-denitrifiers. Woodchips removed less than half of NO₃⁻ removed by maize cobs, but provided ideal conditions for denitrifying bacteria, and adverse effects were not observed. Therefore we recommend the combination of maize cobs and woodchips to enhance NO₃⁻ removal while minimizing adverse effects in denitrification beds.     

A novel control method for nitritation: The domination of ammonia-oxidizing bacteria by high concentrations of inorganic carbon in an airlift-fluidized bed reactor

A novel nitritation method based on the addition of inorganic carbon (IC) was verified using an airlift-fluidized bed reactor packed with sponge cubes. A continuous-treatment experiment demonstrated that the type of nitrification—nitrite or nitrate accumulation—could be controlled by the addition of different alkalinity sources (NaHCO₃ or NaOH, respectively). The maximum rate of ammonia oxidation at 30 °C was 2.47 kg-N/(m³ d), with nitrate formation of less than 0.5% of the converted ammonia. Nitrite accumulation of over 90% was maintained stably over 250 days at 30 °C and was achieved even at 19 °C. Qualitative and quantitative shifts of nitrifying bacteria in the biofilm were monitored by real-time PCR and T-RFLP analysis. Ammonia-oxidizing bacteria (AOB) were dominant but nitrite-oxidizing bacteria (NOB) were eliminated in the reactor when NaHCO₃ was used as the alkalinity source. From the kinetic data, we inferred that high IC concentrations drive stable nitritation by promoting a higher growth rate for AOB than for NOB.     

Dynamics of nitric oxide and nitrous oxide emission during full-scale reject water treatment

Emission of NO and N2O from a full-scale two-reactor nitritation-anammox process was determined during a measurement campaign at the Dokhaven-Sluisjesdijk municipal WWTP (Rotterdam, NL). The NO and N2O levels in the off-gas responded to the aeration cycles and the aeration rate of the nitritation reactor, and to the nitrite and dissolved oxygen concentration. Due to the strong fluctuations in the NO and N2O levels in both the nitritation and the anammox reactor, only time-dependent measurements could yield a reliable estimate of the overall NO and N2O emissions. The NO emission from the nitritation reactor was 0.2% of the nitrogen load and the N2O emission was 1.7%. The NO emission from the anammox reactor was determined to be 0.003% of the nitrogen load and the N2O emission was 0.6%. Emission of NO2 could not be detected from the nitritation-anammox system. Denitrification by ammonia-oxidizing bacteria was considered to be the most probable cause of NO and N2O emission from the nitritation reactor. Since anammox bacteria have not been shown to produce N2O under physiological conditions, it is also suspected that ammonia-oxidizing bacteria contribute most to N2O production in the anammox reactor. The source of NO production in the anammox reactor can be either anammox bacteria or denitrification by heterotrophs or ammonia-oxidizing bacteria. Based on the results and previous work, it seems that a low dissolved oxygen or a high nitrite concentration are the most likely cause of elevated NO and N2O emission by ammonia-oxidizing bacteria. The emission was compared with measurements at other reject water technologies and with the main line of the Dokhaven-Sluisjesdijk WWTP. The N2O emission levels in the reject water treatment seem to be in the same range as for the main stream of activated sludge processes. Preliminary measurements of the N2O emission from a one-reactor nitritation-anammox system indicate that the emission is lower than in two-reactor systems.     

Removal of residual dissolved methane gas in an upflow anaerobic sludge blanket reactor treating low-strength wastewater at low temperature with degassing membrane

In this study, we investigated the efficiency of dissolved methane (D-CH₄) collection by degasification from the effluent of a bench-scale upflow anaerobic sludge blanket (UASB) reactor treating synthetic wastewater. A hollow-fiber degassing membrane module was used for degasification. This module was connected to the liquid outlet of the UASB reactor. After chemical oxygen demand (COD) removal efficiency of the UASB reactor became stable, D-CH₄ discharged from the UASB reactor was collected. Under 35 °C and a hydraulic retention time (HRT) of 10 h, average D-CH₄ concentration could be reduced from 63 mg COD L⁻¹ to 15 mg COD L⁻¹; this, in turn, resulted in an increase in total methane (CH₄) recovery efficiency from 89% to 97%. Furthermore, we investigated the effects of temperature and HRT of the UASB reactor on degasification efficiency. Average D-CH₄ concentration was as high as 104 mg COD L⁻¹ at 15 °C because of the higher solubility of CH₄ gas in liquid; the average D-CH₄ concentration was reduced to 14 mg COD L⁻¹ by degasification. Accordingly, total CH₄ recovery efficiency increased from 71% to 97% at 15 °C as a result of degasification. Moreover, degasification tended to cause an increase in particulate COD removal efficiency. The UASB reactor was operated at the same COD loading rate, but different wastewater feed rates and HRTs. Although average D-CH₄ concentration in the UASB reactor was almost unchanged (ca. 70 mg COD L⁻¹) regardless of the HRT value, the CH₄ discharge rate from the UASB reactor increased because of an increase in the wastewater feed rate. Because the D-CH₄ concentration could be reduced down to 12 ± 1 mg COD L⁻¹ by degasification at an HRT of 6.7 h, the CH₄ recovery rate was 1.5 times higher under degasification than under normal operation.     

Reactivation performance of aerobic granules under different storage strategies

Aerobic granules storage process is complicated and the affective mechanism is not very clear, which is influenced by storage temperature, storage substrate and storage time. The effects of storage temperature (−25 °C, 4 °C and room temperature) and storage substrate (distilled water and 400 mg/L glucose solution) on long-term storage and subsequently reactivation performance of aerobic granules were investigated in this study. The results showed that storage temperature had huge impact on the morphology and physical properties and storage substrate had relatively small influence on granules. Granules reactivation was a re-stability process of granules structure, physical properties and microbial communities. Storage at 4 °C was more suitable for maintenance of structural integrity and granules long-term stability storage. Granules stored at −25 °C achieved excellent settling ability after reactivation and PN/PS ratio was basically unchanged, which demonstrated that storage at −25°Cwas more suitable for the maintenance of the internal microstructure. Aerobic granules under different storage conditions could be reactivated after 10 days operation and the microbial activity (SOUR) could be fully restored. Furthermore granules stored at 4 °C obtained the best recovery performance, and granules at room temperature presented the worst restoration performance. In conclusion, no matter what the storage temperature or the storage substrate is, aerobic granules after long-term storage (8 months) could be restored within 10 days and stored granules could be successfully used as bioseed for reactor fast startup.     

Partial ammonium oxidation to nitrite of high ammonium content urban landfill leachates

In an effort to treat N-rich streams in a more sustainable way, recent years have seen the development of new technologies, most of which are based on autotrophic denitrification via nitrite (anammox). In order to attain a suitable influent for that process, the wastewater must be treated by partially oxidising the ammonium to nitrite. In that aspect, this article presents the start-up and operation of a Partial Nitritation Sequencing Batch Reactor (PN-SBR) treating urban landfill leachates. Stable partial nitritation has been reached treating high ammonium loads (1-1.5 kg Nm(-3)d(-1)), demonstrating the feasibility of this technology as a previous step of anammox process. This study has also given away the importance of pH influence over ammonium oxidising bacteria (AOB) activity, thus it has been possible to determine the values of the half inhibition constants for free ammonia (k(I,FA)=605.48+/-87.18 mg N-NH L(-1)) and free nitrous acid (k(I,FNA)=0.49+/-0.09 mg N-HNO2 L(-1)), as well as the half-saturation constant for bicarbonate (k(HCO3-) = 0.01 +/- 0.16 mg CL(-1)).     

Pre-treatment mechanisms during thermophilic-mesophilic temperature phased anaerobic digestion of primary sludge

Pre-treatment is used extensively to improve degradability and hydrolysis rate of material being fed into digesters. One emerging process is temperature phased anaerobic digestion (TPAD), which applies a short (2 day) 50-70 °C pre-treatment step prior to 35 °C digestion in the main stage (10-20 days). In this study, we evaluated a thermophilic-mesophilic TPAD against a mesophilic-mesophilic TPAD treating primary sludge. Thermophilic-mesophilic TPAD achieved 54% VS destruction compared to 44% in mesophilic-mesophilic TPAD, with a 25% parallel increase in methane production. Measurements of soluble COD and NH₄⁺-N showed increased hydrolysis extent during thermophilic pre-treatment. Model based analysis indicated the improved performance was due to an increased hydrolysis coefficient rather than an increased inherent degradability, suggesting while TPAD is suitable as an intensification process, a larger main digester could achieve similar impact.     

The effect of pH on N2O production under aerobic conditions in a partial nitritation system

Ammonia-oxidising bacteria (AOB) are a major contributor to nitrous oxide (N₂O) emissions during nitrogen transformation. N₂O production was observed under both anoxic and aerobic conditions in a lab-scale partial nitritation system operated as a sequencing batch reactor (SBR). The system achieved 55 ± 5% conversion of the 1 g NH₄⁺-N/L contained in a synthetic anaerobic digester liquor to nitrite. The N₂O emission factor was 1.0 ± 0.1% of the ammonium converted. pH was shown to have a major impact on the N₂O production rate of the AOB enriched culture. In the investigated pH range of 6.0-8.5, the specific N₂O production was the lowest between pH 6.0 and 7.0 at a rate of 0.15 ± 0.01 mg N₂O-N/h/g VSS, but increased with pH to a maximum of 0.53 ± 0.04 mg N₂O-N/h/g VSS at pH 8.0. The same trend was also observed for the specific ammonium oxidation rate (AOR) with the maximum AOR reached at pH 8.0. A linear relationship between the N₂O production rate and AOR was observed suggesting that increased ammonium oxidation activity may have promoted N₂O production. The N₂O production rate was constant across free ammonia (FA) and free nitrous acid (FNA) concentrations of 5-78 mg NH₃-N/L and 0.15-4.6 mg HNO₂-N/L, respectively, indicating that the observed pH effect was not due to changes in FA or FNA concentrations.     

Source water quality effects on monochloramine inactivation of adenovirus, coxsackievirus, echovirus, and murine norovirus

There is a need for more information regarding monochloramine disinfection efficacy for viruses in water. In this study, monochloramine disinfection efficacy was investigated for coxsackievirus B5 (CVB5), echovirus 11 (E11), murine norovirus (MNV), and human adenovirus 2 (HAdV2) in one untreated ground water and two partially treated surface waters. Duplicate disinfection experiments were completed at pH 7 and 8 in source water at concentrations of 1 and 3 mg/L monochloramine at 5 and 15 °C. The Efficiency Factor Hom (EFH) model was used to calculate CT values (mg-min/L) required to achieve 2-, 3-, and 4-log₁₀ reductions in viral titers. In all water types, monochloramine disinfection was most effective for MNV, with 3-log₁₀ CT values at 5 °C ranging from 27 to 110. Monochloramine disinfection was least effective for HAdV2 and E11, depending on water type, with 3-log₁₀ CT values at 5 °C ranging from 1200 to 3300 and 810 to 2300, respectively. Overall, disinfection proceeded faster at 15 °C and pH 7 for all water types. Inactivation of the study viruses was significantly different between water types, but there was no indication that overall disinfection efficacy was enhanced or inhibited in any one water type. CT values for HAdV2 in two types of source water exceeded federal CT value recommendations in the US. The results of this study demonstrate that water quality impacts the inactivation of viruses and should be considered when developing chloramination plans.     

Oxygen-limited autotrophic nitrification-denitrification (OLAND) in a rotating biological contactor treating high-salinity wastewater

A lab-scale rotating biological contactor (RBC) reactor operated under OLAND conditions was slowly adapted during 178 days to increasing salt concentrations going up to 30 g NaCl L(-1). The reactor performed well during this experimental period. However, the removal capacity of the reactor was lower under high-salinity conditions. A removal efficiency of 84% was achieved at a N loading rate of 725 mg N L(-1) d(-1) and a salt concentration of 30 g L(-1). The effect of salt shock loading and adaptation to 30 g NaCl L(-1) on the specific nitritation and anammox activity of the biomass was investigated in short-term batch experiments. A salt shock loading of 30 g L(-1) caused a 43% decrease in specific nitritation activity and 96% loss of specific anammox activity compared to reference biomass (not exposed to salt). The salt-adapted biomass (3-4 weeks) showed a specific nitritation activity that was 23% lower, and a specific anammox activity that was 58% lower, compared to the reference biomass. Overall, these results demonstrate that the OLAND process can have the potential to treat ammonium-rich brines after adaptation to high salinity.