Chemolithotrophic denitrification with elemental sulfur for groundwater treatment

Denitrification for the treatment of nitrates in wastewater typically relies on organic electron donating substrates. However, for groundwater treatment, inorganic compounds such as elemental sulfur (S0) are being considered as alternative electron donors in order to overcome concerns that residual organics can cause biofouling. In this study, a packed-bed bioreactor supplied with S0:limestone granules (1:1, v/v) was started up utilizing a chemolithotrophic denitrifying enrichment culture in the form of biofilm granules that was pre-cultivated on thiosulfate. The granular enrichment culture enabled a rapid start-up of the bioreactor. A nearly complete removal of nitrate (7.3 mM) was NO3- attained by the bioreactor at nitrate loading rates of up to 21.6 mmol/(L(reactor)d). With lower influent concentrations (1.3 mM nitrate) comparable to those found in contaminated groundwater, high nitrate loads of 18.1 mmol/(L(reactor)d) were achieved with an average nitrate removal efficiency of 95.9%. The recovery of nitrogen as benign N2 gas was nearly stoichiometric. The concentration of undesirable products from S0-based denitrification such as nitrite and sulfide were low. Comparison of bioreactor results with batch kinetic studies revealed that denitrification rates were dependent on the surface area of the added S0. The surface area normalized denitrification rate was determined to be 26.4 mmol /(m2 S0 d).     

进水N/S值对同步脱硫反硝化特性的影响

研究了不同进水N/S值条件下,不同接种物的厌氧体系的同步脱硫反硝化特性。结果表明:在N/S为0.6或0.4的条件下,3个体系对硫化物的去除率均达到90%以上,其中以进水N/S为0.4时产生的悬浮态硫最多;硝态氮的去除特性与硫化物不同,3个体系对硝态氮的去除率均在进水N/S为1.0时达到100%,且此时N2的产量也最大。可见,尽管同步脱硫反硝化工艺具备同时脱氮及除硫的能力,但其进水N/S的控制值却不相同。对于脱硫而言,最佳的进水N/S为0.4;对于脱氮而言,最佳的进水N/S为1.0。此外,研究发现3个不同接种物的厌氧体系对硫化物及硝态氮的去除途径不同,进水N/S值的影响也有差异。对于接种了厌氧污泥的体系,存在自养反硝化和异养反硝化的竞争,改变进水N/S值可调节二者的竞争,高N/S值会抑制硫化物自养反硝化过程,降低对硫化物的去除率;对于接种脱氮硫杆菌的纯菌体系,多硫自催化反应会与硫化物自养反硝化反应竞争硫化物,降低对硝态氮的去除率,高N/S值会导致出水硝态氮浓度较高;对于添加脱氮硫杆菌的强化厌氧污泥体系,以硫化物自养反硝化过程为主,最佳的N/S为0.4。     

进水氨氮对厌氧同步脱氮除硫工艺的影响

通过比较含氨氮和不含氨氮两种进水水质条件下接种物不同的两个反应器的脱氮除硫特性,研究进水氨氮对厌氧同步脱氮除硫性能的影响。结果表明,进水未加氨氮的反应器对硫化物和硝态氮的去除率均高达95%,当加入氨氮后,仅有40%～50%的硝态氮被去除,消耗1 g硫化物所还原的硝态氮量减少,去除硝态氮的能力降低了近50%,然而对硫化物的去除率仍维持在90%左右,表明脱氮过程比脱硫过程受进水氨氮的影响大。扫描电镜观察结果证实,当进水中存在氨氮时硫化物的毒性增大,杀死了大量的脱氮硫杆菌,降低了硫化物转化为单质硫的能力,干扰了系统的反硝化脱氮过程,这是导致体系脱氮能力降低的主要原因。     

Denitrification of groundwater with elemental sulfur

Autotrophic denitrification was studied in laboratory columns packed with granular elemental sulfur only and operated in an upflow mode. Soluble inorganic carbon, sodium bicarbonate, was supplied as source of carbon for microbial growth. Denitrification rates of up to 0.20 kg N removed m(-3) d(-1) were obtained at a hydraulic retention time of I h, and a nitrate loading of 0.24 kg N m(-3) d(-1). The process is extremely simple, stable and easy to maintain.     

Simultaneous carbon and nitrogen removal from high strength domestic wastewater in an aerobic RBC biofilm

High strength domestic wastewater discharges after no/partial treatment through sewage treatment plants or septic tank seepage field systems have resulted in a large build-up of groundwater nitrates in Rajasthan, India. The groundwater table is very deep and nitrate concentrations of 500-750 mg/l (113-169 as NO3(-)-N) are commonly found. A novel biofilm in a 3-stage lab-scale rotating biological contactor (RBC) was developed by the incorporation of a sulphur oxidising bacterium Thiosphaera pantotropha which exhibited high simultaneous removal of carbon and nitrogen in fully aerobic conditions. T. pantotropha has been shown to be capable of simultaneous heterotrophic nitrification and aerobic denitrification thereby helping the steps of carbon oxidation, nitrification and denitrification to be carried out concurrently. The first stage having T. pantotropha dominated biofilm showed high carbon and NH4(+)-N removal rates of 8.7-25.9 g COD/m2 d and 0.81-1.85 g N/m2 d for the corresponding loadings of 10.0-32.0 g COD/m2 d and 1.0-3.35 g N/m2 d. The ratio of carbon removed to nitrogen removed was close to 12.0. The nitrification rate increased from 0.81 to 1.8 g N/m2 d with the increasing nitrogen loading rates despite a high simultaneous organic loading rate. However, it fell to 1.53 g N/m2 d at a high load of 3.35 g N/m2 d and 32 g COD/m2 d showing a possible inhibition of the process. A simultaneous 44-63% removal of nitrogen was also achieved without any significant NO2(-)-N or NO3(-)-N build-up. The second and third stages, almost devoid of any organic carbon, acted only as autotrophic nitrification units, converting the NH4(+)-N from stage 1 to nitrite and nitrate. Such a system would not need a separate carbon oxidation step to increase nitrification rates and no external carbon source for denitrification. The alkalinity compensation during denitrification for that destroyed in nitrification may also result in a high economy.     

DEAMOX--new biological nitrogen removal process based on anaerobic ammonia oxidation coupled to sulphide-driven conversion of nitrate into nitrite

This paper reports about the successful laboratory testing of a new nitrogen removal process called DEAMOX (DEnitrifying AMmonium OXidation) for treatment of typical strong nitrogenous wastewater such as baker's yeast effluent. The concept of this process combines the recently discovered anammox (anaerobic ammonium oxidation) reaction with autotrophic denitrifying conditions using sulphide as an electron donor for the production of nitrite from nitrate within an anaerobic biofilm. To generate sulphide and ammonia, a Upflow Anaerobic Sludge Bed (UASB) reactor was used as a pre-treatment step. The UASB effluent was split and partially fed to a nitrifying reactor (to generate nitrate) and the remaining part was directly fed to the DEAMOX reactor where this stream was mixed with the nitrified effluent. Stable process performance and volumetric nitrogen loading rates of the DEAMOX reactor well above 1000 mgN/l/d with total nitrogen removal efficiencies of around 90% were obtained after long-term (410 days) optimisation of the process. Important prerequisites for this performance are appropriate influent ratios of the key species fed to the DEAMOX reactor, namely influent N-NO(x)/N-NH(4) ratios >1.2 (stoichiometry of the anammox reaction) and influent S-H(2)S/N-NO(3) ratios >0.57 mgS/mgN (stoichiometry of the sulphide-driven denitrification of nitrate to nitrite). The paper further describes some characteristics of the DEAMOX sludge as well as the preliminary results of its microbiological characterisation.     

Simultaneous methanogenesis and denitrification of pretreated effluents from a fish canning industry

A lab-scale hybrid upflow sludge bed-filter (USBF) reactor was employed to carry out methanogenesis and denitrification of the effluent from an anaerobic industrial reactor (EAIR) in a fish canning industry. The reactor was initially inoculated with methanogenic sludge and there were two different operational steps. During the first step (Step I: days 1-61), the methanogenic process was carried out at organic loading rates (OLR) of 1.0-1.25 g COD l-1 d-1 reaching COD removal percentages of 80%. During the second step (Step II: days 62-109) nitrate was added as KNO3 to the industrial effluent and the OLR was varied between 1.0 and 1.25 g COD l-1 d-1. Two different nitrogen loads of 0.10 and 0.22 g NO3(-)-N l-1 d-1 were applied and these led to nitrogen removal percentages of around 100% in both cases and COD removal percentages of around 80%. Carbon to nitrogen ratio (C:N) in the influent was maintained at 2.0 and eventually it was increased to 3.0, by means of glucose addition, to control the denitrification process. From these results it is possible to establish that wastewater produced in a fish canning industry can be used as a carbon source for denitrification and that denitrifying microorganisms were present in the initially methanogenic sludge. Biomass productions of 0.23 and 0.61 g VSS:g TOC fed for Steps I and II, respectively, were calculated from carbon global balances, showing an increase in biomass growth due to denitrification.     

Microbial fuel cells for simultaneous carbon and nitrogen removal

The recent demonstration of cathodic nitrate reduction in a microbial fuel cell (MFC) creates opportunities for a new technology for nitrogen removal from wastewater. A novel process configuration that achieves both carbon and nitrogen removal using MFC is designed and demonstrated. The process involves feeding the ammonium-containing effluent from the carbon-utilising anode to an external biofilm-based aerobic reactor for nitrification, and then feeding the nitrified liquor to the MFC cathode for nitrate reduction. Removal rates up to 2 kg COD m(-3)NCC d(-1) (chemical oxygen demand: COD, net cathodic compartment: NCC) and 0.41 kg NO(3)(-)-Nm(-3)NCC d(-1) were continuously achieved in the anodic and cathodic compartment, respectively, while the MFC was producing a maximum power output of 34.6+/-1.1 Wm(-3)NCC and a maximum current of 133.3+/-1.0 Am(-3)NCC. In comparison to conventional activated sludge systems, this MFC-based process achieves nitrogen removal with a decreased carbon requirement. A COD/N ratio of approximately 4.5 g COD g(-1) N was achieved, compared to the conventionally required ratio of above 7. We have demonstrated that also nitrite can be used as cathodic electron acceptor. Hence, upon creating a loop concept based on nitrite, a further reduction of the COD/N ratio would be possible. The process is also more energy effective not only due to the energy production coupled with denitrification, but also because of the reduced aeration costs due to minimised aerobic consumption of organic carbon.     

Combined bioelectrochemical and sulfur autotrophic denitrification for drinking water treatment

A combined bioelectrochemical and sulfur autotrophic denitrification process for drinking water treatment was put forward and investigated extensively in this paper. In this new process, the bioelectrochemical denitrification was carried out in the upper part of the reactor while sulfur denitrification in the lower part. The H+ produced in Sulfur Part could be consumed by hydrogen denitrification in Bioelectrochemical Part. Therefore, the limestone for pH adjustment in Sulfur Part was not necessary in this combined process, which avoided the problem of hardness increase. The sulfate accumulation in this combined reactor was less than that of the sulfur limestone autotrophic denitrification system. The effluent from two parts was kept neutral at optimum operation conditions. When the influent nitrate was 30 mg-N/L, the reactor could be operated efficiently at the hydraulic retention time ranged from 1.9 to 5h (corresponding minimum current was 16-3 mA), i.e. the effluent NO3(-)-N removal ranged from 90% to 100% without nitrite accumulation and the effluent sulfate concentration was lower than 170 mg/L. The maximum volume-loading rate of the reactor was 0.381 kg NO3(-)-N/(m3d). The biomass and scanning electron microscope micrographs of Sulfur Part were also analyzed.     

Organic matter removal in combined anaerobic-aerobic fixed-film bioreactors

A combination of two fixed-film bioreactors (FFB) with arranged media, the first anaerobic and the second aerobic, connected in series with recirculation was fed continuously for 133 days with wastewater from a poultry slaughterhouse. Oxidation of the organic carbon compounds and nitrification were carried out in the aerobic FFB and methanogenesis and denitrification were performed in the anaerobic FFB. The average organic loading rate was 0.39 kg COD/m3d and 92% removal efficiencies of organic matter were achieved. COD-removal occurred mainly in the anaerobic FFB, increasing when the recirculation ratio rose from 1 to 6 due to the increase in the anoxic denitrification. The influence of the C/N ratio of the raw wastewater over the proportion in which the COD-removal was carried out by oxidation in the aerobic FFB, methanogenesis or denitrification in the anaerobic FFB was studied. When the volume of the aerobic FFB became smaller than that of the anaerobic one the fraction of organic matter removed in the anaerobic FFB increased, but also the ratio between the respective volumetric rates (rCODan/rCODae) increased. High recirculation and low C/NO-N ratio in the anaerobic FFB feed favoured the denitrification to the detriment of the methanogenic process. Regarding nitrogen removal for nitrogen applied loads around 0.064 kg TKN/m3d the removal efficiency was of 95%, which decreased to 84% for 0.14 kg TKN/m3d. The stability of the nitrification process was the controlling factor of the nitrogen removal. High ammonia concentration caused by high recirculation ratio, specially when the aerobic FFB volume was smaller, caused nitrification inhibition which destabilised the system.     

好氧颗粒污泥技术用于味精废水处理的研究

以厌氧颗粒污泥为接种污泥,采用人工模拟废水在SBR反应器内培养好氧颗粒污泥,35 d后颗粒污泥成熟,反应器对COD和NH4+-N的去除率分别高于95%和99%。采用该反应器处理味精废水,当COD、NH4+-N的容积负荷分别为2.4、0.24 kg/(m3.d)时,对COD、NH4+-N和TN的去除率分别在90%、99%和85%左右,且颗粒污泥未出现解体的现象。以厌氧颗粒污泥为接种污泥、味精废水为进水,在与上述相同条件下培养好氧颗粒污泥,经过60 d的培养,反应器内的污泥以絮状污泥为主,该系统对COD、NH4+-N和TN的去除率分别为85%、99%和70%。     

Integrated anaerobic-aerobic fixed-film reactor for slaughterhouse wastewater treatment

An integrated anaerobic-aerobic fixed-film pilot-scale reactor with arranged media was fed during 166 days with slaughterhouse wastewater. Operation temperature was 25 degrees C and the anaerobic-aerobic volume ratio was decreased from 4:1 to 3:2 and finally to 2:3. Overall organic matter removal efficiencies of 93% were achieved for an average organic loading rate of 0.77 kg COD/m3 d, and nitrogen removal efficiencies of 67% were achieved for nitrogen loading rates of 0.084 kg N/m3 d. The high internal recirculation associated to the air-lift effect linked to the aeration of a part of the reactor section caused high mixing between the anaerobic and aerobic zones, so that most organic matter was removed aerobically. The nitrification process achieved an efficiency of 91% for nitrogen loads of 0.15 kg N/m3 d when the anaerobic-aerobic volume ratio was 2:3 and was limited by dissolved oxygen concentration below 3 mg/l. The influence of the heterotrophic biomass growing in the outer biofilm was checked. Denitrification only implied the 12-34% of the total nitrogen removal and was limited by dissolved oxygen concentration in the anaerobic zone above 0.5 mg/l caused by the mixing regime. Most removed nitrogen was employed in synthesis of heterotrophic bacteria.     

Improved brine recycling during nitrate removal using ion exchange

Ion exchange technology is currently the best for removing nitrate from drinking water. However, problems related to the disposal of spent brine from regeneration of exhausted resins must be overcome so that ion exchange can be applied more widely and economically, especially in small communities. For this purpose, a novel spent brine recycling system using combined biological denitrification and sulfate reduction processes was developed for more efficient reuse of brine. A granular activated carbon (GAC) adsorption column was introduced as an additional step to prevent contamination of resins by bio-polymers and dissolved organics present in the bio-reactor effluent. Two upflow sludge blanket reactors (USBRs) were operated in series for 166 days to provide denitrification and sulfate reduction. The denitrification reactor provided a nitrate removal efficiency of 96% at a nitrate-N loading rate of 5.4 g NO3(-)-N/l d. The sulfate reduction efficiency of the sulfate reduction reactor remained approximately 62% at a sulfate loading rate of 1.8 g SO4(2-)/l d. Five ion exchange columns containing A520E resins were repeatedly operated in up to 25 cycles of service and regeneration using five kinds of brine: one virgin 3% NaCl and four differently recycled spent brines. Throughput decreased remarkably when the biologically recycled brine was not treated with the GAC column, probably due to the presence of bio-polymers and dissolved organic compounds. The sulfate reduction reactor placed after the denitrification step increased the bicarbonate concentration, which could be used as a co-regenerant with chloride. The inclusion of the sulfate reduction reactor into the conventional brine recycling system allowed more efficient reuse of brine, resulting in both reduced salt consumption and brine discharge.     

Removal of ammonia from contaminated air in a biotrickling filter - denitrifying bioreactor combination system

The removal of gaseous ammonia in a system consisting of a biotrickling filter, a denitrification reactor and a polishing bioreactor for the trickling liquid was investigated. The system allowed sustained treatment of ammonia while preventing biological inhibition by accumulating nitrate and nitrite and avoiding generation of contaminated water. All bioreactors were packed with cattle bone composite ceramics, a porous support with a large interfacial area. Excellent removal of ammonia gas was obtained. The critical loading ranged from 60 to 120 gm(-3)h(-1) depending on the conditions, and loadings below 56 gm(-3)h(-1) resulted in essentially complete removal of ammonia. In addition, concentrations of ammonia, nitrite, nitrate and COD in the recycle liquid of the inlet and outlet of each reactor were measured to determine the fate of nitrogen in the reactor, close nitrogen balances and calculate nitrogen to COD ratios. Ammonia absorption and nitrification occurred in the biotrickling filter; nitrate and nitrite were biologically removed in the denitrification reactor and excess dissolved COD and ammonia were treated in the polishing bioreactor. Overall, ammonia gas was very successfully removed in the bioreactor system and steady state operation with respect to nitrogen species was achieved.     

Simultaneous organic and nitrogen removal from municipal landfill leachate using an anaerobic-aerobic system

An anaerobic-aerobic system including simultaneous methanogenesis and denitrification was introduced to treat organic and nitrogen compounds in immature leachate from a landfill site. Denitrification and methanogenesis were successfully carried out in the anaerobic reactor while the organic removal and nitrification of NH4+,-N were carried out in the aerobic reactor when rich organic substrate was supplied with appropriate hydraulic retention time. The maximum organic removal rate was 15.2 kg COD/m3 d in the anaerobic reactor while the maximum NH4+-N removal rate and maximum nitrification rate were 0.84kg NH4+-N/m3/d and 0.50kg NO3--N/m3/d, respectively, in the aerobic reactor. The pH range for proper nitrification was 6-8.8 in the aerobic reactor. The organic compounds inhibited nitrification so that the organic removal in the anaerobic reactor could enhance the nitrification rate in the following aerobic reactor. The gas production rate was 0.33 m3/kg COD and the biogas compositions of CH4, CO2, and N2 were kept relatively constant, 66-75, 22-32, and 2-3%, respectively.     

Sulfide-induced nitrate reduction in the sludge of an anaerobic digester of a zero-discharge recirculating mariculture system

The anaerobic digester is a vital component in a zero-discharge mariculture system as therein most of the organic matter is mineralized and nitrogen-containing compounds are converted to gaseous N₂. Although denitrification is a major respiratory process in this nitrate-rich treatment stage, also sulfate respiration takes place and may cause undesirable high sulfide concentrations in the effluent water. To examine the effect of sulfide on nitrate reduction, in situ depth profiles of inorganic nitrogen and sulfur compounds were determined. Additionally, nitrate reduction was examined as a function of ambient sulfide concentrations in sludge collected from different locations in the anaerobic reactor. Depth profiles showed high concentrations of nitrate and low concentrations of sulfide and ammonia in the aqueous layer of the reactor. A sharp decrease of nitrate and an increase in sulfide and ammonia concentrations was measured at the water-sludge interface. Nitrate reduction was highest in this interface zone with rates of up to 8.05 ± 0.57 μmol NO₃⁻ h⁻¹ g_(sludge)⁻¹. Addition of sulfide increased the nitrate reduction rate at all sludge depths, pointing to the important role of autotrophic denitrification in the anaerobic reactor. Dissimilatory nitrate reduction to ammonia (DNRA) was found to be low in all sludge layers but was enhanced when sludge was incubated at high sulfide concentrations. Although nitrate reduction rates increased as a result of sulfide addition to sludge samples, no differences in nitrate reduction rates were observed between the samples incubated with different initial sulfide concentrations. This as opposed to sulfide oxidation rates, which followed Michaelis-Menten enzymatic kinetics. Partial oxidation of sulfide to elemental sulfur instead of a complete oxidation to sulfate, could explain the observed patterns of nitrate reduction and sulfide oxidation in sludge incubated with different initial sulfide concentrations.     

Macroscale and microscale analyses of nitrification and denitrification in biofilms attached on membrane aerated biofilm reactors

A membrane aerated biofilm reactor (MABR), in which O(2) was supplied from the bottom of the biofilm and NH(4)(+) and organic carbon were supplied from the biofilm surface, was operated at different organic carbon loading rates and intra-membrane air pressures to investigate the occurrence of simultaneous chemical oxygen demand (COD) removal, nitrification and denitrification. The spatial distribution of nitrification and denitrification zones in the biofilms was measured with microelectrodes for O(2), NH(4)(+), NO(2)(-), NO(3)(-) and pH. When the MABR was operated at approximately 1.0 g-COD/m(2)/day of COD loading rate, simultaneous COD removal, nitrification and denitrification could be achieved. The COD loading rates and the intra-membrane air pressures applied in this study had no effect on the start-up and the maximum rates of NH(4)(+) oxidation in the MABRs. Microelectrode measurements showed that O(2) was supplied from the bottom of the MABR biofilm and penetrated the whole biofilm. Because the biofilm thickness increased during the operations, an anoxic layer developed in the upper parts of the mature biofilms while an oxic layer was restricted to the deeper parts of the biofilms. The development of the anoxic zones in the biofilms coincided with increase in the denitrification rates. Nitrification occurred in the zones from membrane surface to a point of ca. 60microm. Denitrification mainly occurred just above the nitrification zones. The COD loading rates and the intra-membrane air pressures applied in this study had no effect on location of the nitrification and denitrification zones.     

Sulfide removal in wastewater from petrochemical industries by autotrophic denitrification

An alternative flowchart for the biological removal of hydrogen sulfide from oil-refining wastewater is presented; autotrophic denitrification in a multi-stage treatment plant was utilized. A pilot-scale plant was fed with a mixture of the following constituents: (a) original wastewater from an oil refining industry (b), the effluent of the existing nitrification-stage treatment plant and (c) sulfide in the form of Na2S. Anoxic sulfide to sulfate oxidation, with nitrate as a terminal electron acceptor, proved very successful, as incoming concentrations of 110 mg S2-/L were totally converted to SO(4)2-. At complete denitrification, the concentration of S2- in the reactor effluent was less than 0.1mg/L. Fluctuating S2- concentration in the feed could be tolerated without any problems, as the accumulated sulfide in the effluent of the denitrification stage is oxidized aerobically in a subsequent activated-sludge treatment stage. This alternative new treatment scheme was further introduced at the refinery's wastewater processing plant. Thus, complete H2S removal is now accomplished by the combination of the proposed biological method and the existing stripping with CO2. As a result, stripping, and thus its cost, is reduced by 70%.     

Granulation in high-load denitrifying upflow sludge bed (USB) pulsed reactors

In this work, the effect of the application of a pulse system to anoxic upflow sludge bed (USB) denitrifying reactors for enhancing sludge granulation was studied. In all, three 0.8 L reactors (two operated with flow pulsation, P1 with effluent recycling and P2 without recycling, and one without pulsation and effluent recycling, no pulsation (NP)) were fed with a mixture of NaNO3 and glucose and inoculated with methanogenic granular sludge. The organic loading rate (OLR) and the nitrogen loading rate (NLR) were progressively increased and, at the end of the experiment, extremely high values were obtained (67.5 kgCOD/m3d and 11.25 kgN-NO3-/m3 d). Ammonia and nitrite accumulation in reactor NP were important in the maturation stage, decreasing the denitrification efficiency to 90%, while in reactor P1 only low nitrite values were obtained in the last few days of the experiment. In reactor P2, nitrogen removal was 100% most of the time. Several operational problems (flotation and the subsequent wash out of biomass) appeared in the NP reactor when working at high denitrifying loading rates, while in reactors P1 and P2 there were no notable problems, mainly due to the good characteristics of the sludge developed and the efficient degasification produced by the pulsing flow. The sludge formed in the NP reactor presented a flocculent structure and a total disintegration of the initial methanogenic granules occurred, while a small-sized granular biomass with a high specific density was developed in the pulsed reactors due to the shear stress produced.     

沸石SBR/缺氧上升流污泥床实现氧化铁红废水脱氮

采用沸石序批式反应器(ZSBR)与缺氧上升流污泥床反应器(A-USB)组合工艺处理氧化铁红高氨氮废水,探究ZSBR稳定亚硝化特性以及组合工艺的脱氮性能。结果表明,通过游离氨(FA)抑制亚硝酸盐氧化菌(NOB),ZSBR可实现稳定高效的完全亚硝化。在进水NH4+-N浓度约为700 mg/L的情况下,ZSBR的出水NH4+-N基本稳定在30 mg/L以下,亚硝化率(NAR)维持在95%以上,平均亚硝酸盐产率(NPR)最高可达0. 68 kg/(m³·d)。提升外回流比能够有效利用A-USB反硝化产生的碱度并减少ZSBR中碳酸氢钠碱度的投加量。以葡萄糖作为外加碳源进行反硝化试验,ZSBR出水经过A-USB反硝化处理后,总氮去除率(NRE)能够较稳定维持在85%以上,最高总氮去除负荷(NRR)可达5. 10 kg/(m³·d)。高通量测序分析表明,ZSBR样品中AOB(Nitrosomonas)的相对丰度达到了50. 93%,未检测出NOB,而具有反硝化功能的副球菌属、丛毛单胞菌属和假单胞菌属的相对丰度总占比可达7. 05%,进一步验证了组合工艺高效且稳定的脱氮性能。