DEGRADATION OF AROCLOR 1242 IN A SINGLE-STAGE COUPLED ANAEROBIC/AEROBIC BIOREACTOR

Degradation of Aroclor 1242 was studied in granular biofilm reactors with limited aeration. An aerobic biphenyl degrader, Rhodococcus sp. M5, was used to supplement a natural bacterial population present in a “bioaugmented” reactor, while the “non-bioaugmented” reactor only contained natural granular sludge. The bioaugmentation, however appeared to have no effect on the reactor performance. Aroclor measurements showed its disappearance in both reactors with only 16–19% of Aroclor recovered from the reactor biomass and effluent. Simultaneously, a chlorine balance indicated that dechlorination occurred at a specific rate of 1.43 mg PCB (g volatile suspended solids)⁻¹ d⁻¹, which was comparable to the observed rate of Aroclor disappearance. Intermediates detected in both reactors were biphenyl, benzoic acid, and mono-hydroxybiphenyls. This suggests that a near-complete mineralization of Aroclor can be achieved in a single-stage anaerobic/aerobic system due to a combination of reductive and oxidative degradation mechanisms.     

微好氧与厌氧水解酸化对明胶废水的预处理效果

以明胶废水为研究对象,采用微好氧与厌氧水解酸化工艺进行对比处理实验,探讨了不同水力停留时间下微好氧与厌氧水解酸化对明胶废水水质改善的效果。实验结果表明,在水力停留时间达到72h的时候,溶解氧为1.3~1.6mg/L的微好氧反应器的COD去除率最大可达25%,溶解氧为0.3~0.5mg/L的厌氧反应器的COD去除率最大可达22%;微好氧反应器的VFA的含量达到12mg/L左右,厌氧反应器只有8mg/L左右;微好氧反应器的pH值可由最初的12.5降至7.5左右,而厌氧反应器只能降至8.0左右;两个反应器对蛋白质去除效果的差别并不明显,都可以达到90%以上,但是微好氧反应器的氨氮浓度只有22mg/L,小于厌氧反应器中的氨氮浓度,说明微氧条件有利于氨氮的扩散挥发,低浓度的氨氮对微生物的危害较小。对比得出微好氧反应器的出水水质较好,更适合明胶废水水解酸化的预处理。     

The effect of thermal hydrolysis pretreatment on the anaerobic degradation of nonylphenol and short-chain nonylphenol ethoxylates in digested biosolids

The presence of micropollutants can be a concern for land application of biosolids. Of particular interest are nonylphenol diethoxylate (NP₂EO), nonylphenol monoethoxylate (NP₁EO), and nonylphenol (NP), collectively referred to as NPE, which accumulate in anaerobically digested biosolids and are subject to regulation based on the environmental risks associated with them. Because biosolids are a valuable nutrient resource, it is essential that we understand how various treatment processes impact the fate of NPE in biosolids. Thermal hydrolysis (TH) coupled with mesophilic anaerobic digestion (MAD) is an advanced digestion process that destroys pathogens in biosolids and increases methane yields and volatile solids destruction. We investigated the impact of thermal hydrolysis pretreatment on the subsequent biodegradation of NPE in digested biosolids. Biosolids were treated with TH, anaerobic digestion, and aerobic digestion in laboratory-scale reactors, and NPE were analyzed in the influent and effluent of the digesters. NP₂EO and NP₁EO have been observed to degrade to the more estrogenic NP under anaerobic conditions; therefore, changes in the ratio of NP:NPE were of interest. The increase in NP:NPE following MAD was 56%; the average increase of this ratio in four sets of TH-MAD samples, however, was only 24.6 ± 3.1%. In addition, TH experiments performed in pure water verified that, during TH, the high temperature and pressure alone did not directly destroy NPE; TH experiments with NP added to sludge also showed that NP was not destroyed by the high temperature and pressure of TH when in a more complex sludge matrix. The post-aerobic digestion phases removed NPE, regardless of whether TH pretreatment occurred. This research indicates that changes in biosolids processing can have impacts beyond just gas production and solids destruction.     

A~2/O~2生物膜工艺处理焦化废水研究

采用A~2/O~2生物膜工艺处理焦化废水,分别考察了厌氧(A_1)、缺氧(A_2)、一级好氧(O_1)和二级好氧(O_2)反应器对污染物的去除效果.在A_1、A_2、O_1和O_2反应器的HRT分别为15.5、15、12、12 h,水温为20～30℃,pH值为7.0～9.5,回流比为3.0的条件下,各反应器对COD的平均去除率分别为31.0%、27.6%、48.1%和8.2%;在A1中NH_3-N浓度增加了25.2%,A_2、O_1、O_2反应器对NH_3-N的平均去除率分别为6.2%、46.7%和76.7%;系统出水COD、NH_3-N的平均浓度分别为227、11.5 mg/L,对COD、NH_3-N的平均去除率分别为87.2%、94.1%.     

Anaerobic/aerobic treatment of coloured textile effluents using sequencing batch reactors

Conventional biological wastewater treatment plants do not easily degrade the dyes and polyvinyl alcohols (PVOH) in textile effluents. Results are reported on the possible advantages of anaerobic/aerobic cometabolism in sequenced redox reactors. A six phase anaerobic/aerobic sequencing laboratory scale batch reactor was developed to treat a synthetic textile effluent. The wastewater included PVOH from desizing and an azo dye (Remazol Black). The reactor removed 66% of the applied total organic carbon (load F: M 0.15) compared to 76% from a control reactor without dye. Colour removal was 94% but dye metabolites caused reactor instability. Aromatic amines from the anaerobic breakdown of the azo dyes were not completely mineralised by the aerobic phase. Breakdown of PVOH by the reactor (20-30%) was not as good as previous reports with entirely aerobic cultures. The anaerobic cultures were able to tolerate the oxygen and methane continued to be produced but there was a deterioration in settlement.     

Biomass characteristics in three sequencing batch reactors treating a wastewater containing synthetic organic chemicals

The physical and biochemical characteristics of the biomass in three lab-scale sequencing batch reactors (SBR) treating a synthetic wastewater at a 20-day target solids retention time (SRT) were investigated. The synthetic wastewater feed contained biogenic compounds and 22 organic priming compounds, chosen to represent a wide variety of chemical structures with different N, P and S functional groups. At a two-day hydraulic retention time (HRT), the oxidation-reduction potential (ORP) cycled between -100 (anoxic) and 100 mV (aerobic) in the anoxic/aerobic SBR, while it remained in a range of 126+/-18 and 249+/-18 mV in the aerobic sequencing batch biofilm reactor (SBBR) and the aerobic SBR reactor, respectively. A granular activated sludge with excellent settleability (SVI=98+/-31 L mg(-1)) developed only in the anoxic/aerobic SBR, compared to a bulky sludge with poor settling characteristics in the aerobic SBR and SBBR. While all reactors had very good COD removal (>90%) and displayed nitrification, substantial nitrogen removal (74%) was only achieved in the anoxic/aerobic SBR. During the entire operational period, benzoate, theophylline and 4-chlorophenol were completely removed in all reactors. In contrast, effluent 3-nitrobenzoate was recorded when its influent concentration was increased to 5 mg L(-1) and dropped only to below 1 mg L(-1) after 300 days of operation. The competent (active) biomass fractions for these compounds were between 0.04% and 5.52% of the total biomass inferred from substrate-specific microbial enumerations. The measured competent biomass fractions for 4-chlorophenol and 3-nitrobenzoate degradation were significantly lower than the influent COD fractions of these compounds. Correspondent to the highest competent biomass fraction for benzoate degradation among the test SOCs, benzoate oxidation could be quantified with an extant respirometric technique, with the highest specific oxygen uptake rate (SOUR(benzoate), 0.026 g O2 h(-1) g(-1) XCOD) in the anoxic/aerobic SBR. These combined results suggest that operating SBRs with alternative anoxic/aerobic cycles might facilitate the formation of granular sludge with good settleability, and retain comparable removal of nitrogen and synthetic organic compounds. Hence, the practice of anoxic/aerobic cycling should be considered in wastewater treatment systems whenever possible.     

Evaluation of continuous mesophilic, thermophilic and temperature phased anaerobic digestion of microwaved activated sludge

The effects of microwave (MW) pretreatment, staging and digestion temperature on anaerobic digestion were investigated in a setup of ten reactors. A mesophilic reactor was used as a control. Its performance was compared to single-stage mesophilic and thermophilic reactors treating pretreated and non-pretreated sludge, temperature-phased (TPAD) thermophilic-mesophilic reactors treating pretreated and non-pretreated sludge and thermophilic-thermophilic reactors also treating pretreated and non-pretreated sludge. Four different sludge retention times (SRTs) (20, 15, 10 and 5 d) were tested for all reactors. Two-stage thermo-thermo reactors treating pretreated sludge produced more biogas than all other reactors and removed more volatile solids. Maximum volatile solids (VS) removal was 53.1% at an SRT of 15 d and maximum biogas increase relative to control was 106% at the shortest SRT tested. Both the maximum VS removal and biogas relative increase were measured for a system with thermophilic acidogenic reactor and thermophilic methanogenic reactor. All the two-stage systems treating microwaved sludge produced sludge free of pathogen indicator bacteria, at all tested conditions even at a total system SRT of only 5 d. MW pretreatment and staging reactors allowed the application of very short SRT (5 d) with no significant decrease in performance in terms of VS removal in comparison with the control reactor. MW pretreatment caused the solubilization of organic material in sludge but also allowed more extensive hydrolysis of organic material in downstream reactors. The association of MW pretreatment and thermophilic operation improves dewaterability of digested sludge.     

Biodegradation of agricultural herbicides in sequencing batch reactors under aerobic or anaerobic conditions

This study investigated the biodegradability of the herbicides isoproturon and 2,4-dichlorophenoxyacetic acid (2,4-D) in sequencing batch reactors (SBRs). Two laboratory-scale (2L liquid volume) SBRs were employed: one reactor performing under aerobic and the other under anaerobic conditions. The aerobic SBR was operated at an ambient temperature (22+/-2 degrees C), while the anaerobic SBR was run in the lower mesophilic range (30+/-2 degrees C). Each bioreactor was seeded with a 3:1 mixture (by weight) of fresh sludge and biomass that had been previously exposed to both herbicides. The effect of herbicide concentration on either treatment process was explored at a hydraulic retention time (HRT) of 48 h, using glucose as a supplemental carbon substrate. Although no isoproturon degradation was observed in either system during the study, complete 2,4-D removal occurred after an acclimation period of approximately 30 d (aerobic SBR) and 70 d (anaerobic SBR). The aerobic reactor achieved complete 2,4-D utilization at feed concentrations up to 500 mg/L. A further increase to 700 mg/L, however, proved to be inhibitory since 2,4-D biodegradation was negligible. On the other hand, the anaerobic SBR was able to degrade 120 mg/L of 2,4-D, which corresponds to 40% of the maximum feed concentration applied. Moreover, glucose was consumed first throughout the experiment in a sequential utilization pattern relating to 2,4-D, with biodegradation of both substrates following closely first-order kinetics.     

Combined anaerobic and aerobic digestion for increased solids reduction and nitrogen removal

A unique sludge digestion system consisting of anaerobic digestion followed by aerobic digestion and then a recycle step where thickened sludge from the aerobic digester was recirculated back to the anaerobic unit was studied to determine the impact on volatile solids (VS) reduction and nitrogen removal. It was found that the combined anaerobic/aerobic/anaerobic (ANA/AER/ANA) system provided 70% VS reduction compared to 50% for conventional mesophilic anaerobic digestion with a 20 day SRT and 62% for combined anaerobic/aerobic (ANA/AER) digestion with a 15 day anaerobic and a 5 day aerobic SRT. Total Kjeldahl nitrogen (TKN) removal for the ANA/AER/ANA system was 70% for sludge wasted from the aerobic unit and 43.7% when wasted from the anaerobic unit. TKN removal was 64.5% for the ANA/AER system.     

Polybrominated diphenyl ethers in sewage sludge and treated biosolids: Effect factors and mass balance

Polybrominated diphenyl ether (PBDE) flame retardants have been consistently detected in sewage sludge and treated biosolids. Two hundred and eighty-eight samples including primary sludge (PS), waste biological sludge (WBS) and treated biosolids from fifteen wastewater treatment plants (WWTPs) in Canada were analyzed to investigate the factors affecting accumulation of PBDEs in sludge and biosolids. Factors examined included environmental/sewershed conditions and operational parameters of the WWTPs. PBDE concentrations in PS, WBS and treated biosolids were 230–82,000 ng/g, 530–8800 ng/g and 420–6000 ng/g, respectively; BDE-209,-99, and -47 were the predominant congeners. Concentrations were influenced by industrial input, leachate, and temperature. Several examinations including the measurement of BDE-202 indicated minimal debromination during wastewater treatment. Estimated solids-liquid distribution coefficients were moderately correlated to hydraulic retention time, solids loading rate, mixed liquor suspended solids, solids retention time, and removal of organic solids, indicating that PBDE partitioning to solids can be optimized by WWTPs' operational conditions. Solids treatment type strongly affected PBDE levels in biosolids: 1.5 times increase after solids digestion, therefore, digestion efficiency could be a potential factor for variability of PBDEs concentration. In contrast, alkaline treatment reduced PBDE concentrations in biosolids. Overall, mass balance approaches confirmed that PBDEs were removed from the liquid stream through partitioning to solids. Variability of PBDE levels in biosolids could result in different PBDEs burdens to agricultural land, and different exposure levels to soil organisms.     

Ozonation reduces sludge production and improves denitrification

The effectiveness of partial ozonation of return activated sludge for enhancing denitrification and waste sludge minimization were examined. A pair of nitrifying sequencing batch reactors was operated in either aerobic or alternating anoxic/aerobic conditions, with one control and one ozonated reactor in each set. The amount of solids produced decreased with the ozone dose. Biomass in the anoxic/aerobic reactor was easier to destroy (up to 25% of the initial excess sludge) than in the aerobic (10%) one, generating approximately twice as much soluble COD by cell lysis. Denitrification rate improved up to 60% due to additional carbon released by ozonation. Nitrification rates deteriorated much more in the aerobic than in the alternating reactor, possibly as a result of direct destruction of nitrifying autotrophs as well as competition created by growth of heterotrophs receiving the additional COD. Overall, ozonation provided the expected benefits in denitrification and had less impact on nitrification in the alternating reactors.     

Effectiveness of an alternating aerobic, anoxic/anaerobic strategy for maintaining biomass activity of BNR sludge during long-term starvation

The effectiveness of an aerobic, anoxic/anaerobic strategy for maintaining the activity of activated sludge performing biological nitrogen and phosphorus removal during long-term starvation is investigated. A lab-scale sequencing batch reactor (SBR) treating abattoir wastewater and achieving high-levels (>95%) of nitrogen, phosphorus and COD removal was used. The reactor was put twice into a so-called "sleeping mode" for a period of 5-6 weeks when the abattoir, where the wastewater was sourced, was closed down for annual maintenance. The "sleeping mode" operation consisted of 15 min aeration in a 6 h SBR cycle. The sludge was allowed to settle in the remaining time of the cycle. The decay rates for ammonia oxidising bacteria (AOB) and nitrite oxidising bacteria (NOB) were determined to be 0.017 and 0.004 d(-1), respectively. These decay rates correlated well with AOB and NOB population quantified using molecular techniques (FISH). There was negligible phosphate accumulation in the reactor during the first 1-2 weeks of starvation, which was followed by a linear net release of phosphate in the remaining 4-5 weeks at a very slow rate of 1-2 mgP gVSS(-1)d(-1). A sudden decrease in the aerobic activities of polyphosphate accumulating organisms (PAOs), observed via anaerobic/aerobic batch tests, occurred after 2 weeks of starvation. This correlated with a dramatic increase of several metal ions in the liquid phase. The underlying reasons are not clear. A resuscitation period with a gradual increase of the wastewater load was applied during the re-startup of the reactor after both "sleeping mode" periods. Each time, the performance of the reactor in terms of nitrogen and phosphorus removal fully recovered in 4 days.     

Performance of temperature-phased anaerobic digestion (TPAD) system treating dairy cattle wastes

The performance of temperature-phased anaerobic digestion (TPAD) system in the stabilization of dairy cattle wastes at high solids concentrations has never been evaluated, though the process has been established as a feasible alternative to conventional mesophilic processes for the treatment of municipal wastewater sludges. In this study, the TPAD system operating at a retention time of 14 days was subjected to varying total solids (TS) concentrations (3.46-14.54%) of dairy cattle wastes. At TS concentrations lower than 12.20%, corresponding to system volatile solids (VS) loadings in the range of 1.87-5.82 g VS/L/day, the system achieved an average VS removal of 40.2%. The maximum VS destruction of 42.6% was achieved at a TS concentration of 10.35%. Methane recovery from the wastes was consistently within 0.21-0.22 L/g VS fed. There was a drop in the system performance with respect to VS removal and methane recovery at TS concentrations higher than 10.35%. volatile fatty acid/alkalinity ratios less than 0.35 in the thermophilic reactor and 0.10 in the mesophilic reactor were found favorable for stable operation of the system. For the entire range of TS concentrations, the indicator organism counts in the biosolids were within the limits specified by USEPA in 40 CFR Part 503 regulations for Class A designation. After digestion, nearly 80-85% of total phosphorus was associated with the biosolids.     

Effects of ferric iron on the anaerobic treatment and microbial biodiversity in a coupled microbial electrolysis cell (MEC) – Anaerobic reactor

Adding Fe(III) into a MEC – anaerobic reactor enhanced the degradation of organic matters. To clarify the respective effects of combining Fe(III) dosage and a MEC and Fe(III) dosage only on strengthening anaerobic digestion, three anaerobic reactors were operated in parallel: a MEC – anaerobic reactor with dosing Fe(OH)₃ (R1), an anaerobic reactor with dosing Fe(OH)₃ (R2) and a common anaerobic reactor (R3). With increasing influent COD from 1500 to 4000 mg/L, the COD removal in R1 was maintained at 88.3% under a voltage of 0.8 V, which was higher than that in reactor R2 and R3. When the power was cut off, the COD removal in R1 decreased by 5.9%. The addition of Fe(OH)₃ enhanced both anaerobic digestion and anodic oxidation, resulting in the effective mineralization of volatile fatty acids (VFAs). The reduced Fe(II) combined with electric field resulted more extracellular polymeric substances (EPS) production. Quantitative real – time PCR showed a higher abundance of bacteria in the anodic biofilm and R1. Pyrosequencing and denaturing gradient gel electrophoresis (DGGE) analysis revealed that the dominant bacteria and archaea communities were richer and more abundant in the anode biofilm and R1.     

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.     

Fate and effect of the antioxidant ethoxyquin on a mixed methanogenic culture

The potential inhibitory effect of ethoxyquin, an antioxidant commonly used as a preservative in the food processing industry (e.g., for stabilizing dissolved air flotation residuals), was evaluated at concentrations up to 300 mg/L using a mixed, mesophilic (35 degrees C) methanogenic culture and dextrin, peptone and methanol as the carbon source. A batch assay conducted with a range of ethoxyquin concentrations did not result in any inhibition up to an ethoxyquin concentration of 75 mg/L, but severe inhibition of methanogenesis was observed at concentrations higher than 150 mg/L. Ethoxyquin addition to a batch reactor with the same mixed, methanogenic culture, at ethoxyquin concentrations gradually increasing over 100 days, resulted in a transient and a complete inhibition of methanogenesis at ethoxyquin concentrations of 150 and 300 mg/L, respectively. Acidogens were not significantly impacted, whereas aceticlastic and methanol degrading methylotrophic methanogens were impacted the most. Acclimation of the methanogenic culture to ethoxyquin was not observed over an incubation period of more than 100 days. Long-term (>100 days) incubation at sub-inhibitory ethoxyquin concentrations did not result in ethoxyquin biotransformation. Similarly, ethoxyquin biotransformation was not evident over an 8-day aeration period in a laboratory-scale activated sludge reactor operated under fully aerobic conditions. Ethoxyquin phase distribution tests conducted with the mixed, methanogenic culture at 1.61 g/L volatile solids concentration and nominal ethoxyquin concentrations equal to or higher than 300 mg/L resulted in solid phase/liquid phase ethoxyquin ratios equal to or higher than 1.0. The combined effect of ethoxyquin recalcitrance under anaerobic conditions along with its phase distribution, which favors biosolids, will result in ethoxyquin accumulation in anaerobic treatment systems used by the food processing industry. Such accumulation may pose concerns relative to inhibitory effects in these treatment systems and the disposal of ethoxyquin-bearing biosolids.     

Decolorizing and detoxifying textile wastewater, containing both soluble and insoluble dyes, in a full scale combined anaerobic/aerobic system

The wastewater originating from the bleaching and dyeing processes in the textile factory Ten Cate Protect in Nijverdal (the Netherlands) was successfully treated in a sequential anaerobic/aerobic system. In the system, a combination of an anaerobic 70-m3 fluidized bed reactor and a 450-m3 aerobic basin with integrated tilted plate settlers, 80-95% of the color was removed. The color was largely removed in the preacidification basin and the anaerobic reactor. Color, deriving from both reactive as well as disperse, was anaerobically removed, indicating that these type of dyes were reduced to colorless products. Interestingly, the vat dyes, the anthraquinones and indigoids, which were thought to be removed mainly aerobically, were largely anaerobically decolorized. Apparently the anaerobic system is capable of effectively removing the color of both soluble as insoluble dyes. The treated effluent of the sequential anaerobic/aerobic treatment showed no toxicity towards the bioluminescent bacterium Vibrio fisheri (EC20 (95%) > 45%). Partially bypassing the anaerobic stage resulted in increased toxicity (EC20 (95%) of 9% and 14%) in the effluent of the aerobic treatment and caused significant decrease of color removal. The results of this study show a main contribution of anaerobic treatment in decolorizing and detoxifying the textile wastewater in the sequential anaerobic/aerobic system.     

Optimierter mikrobiologischer Abbau von Chlorbenzen in <Emphasis Type="Italic">In situ</Emphasis>-Grundwasserreaktoren (SAFIRA)

In two reactors of the SAFIRA pilot plant, the microbial degradation of chlorobenzene (CB) by indigenous bacteria in native aquifer sediment were tested under oxic and anoxic conditions. Under anoxic conditions, no definite degradation was observed. Adding hydrogen peroxide (2.94 mM) and nitrate (2 mM) in one of the two reactors caused the degradation of CB (0.2–0.3 mM) in the lower part of the reactor, accompanied by a clear increase of the number of cultivable aerobic CB-degrading bacteria. After decreasing the hydrogen peroxide concentration to 0.88 mM, the CB concentrations increased in the lower part of the reactor, but decreased later, starting after approximately 100 days, finally under the detection limit again. Less than four mole oxygen were needed for the degradation of one mole CB. No accumulating compounds were determined, which could indicate an incomplete aerobic degradation of CB. These results point out that the oxygen released from hydrogen peroxide was almost completely consumed by bacteria for CB degradation. Nitrate disappeared uniformly during the reactor flow path.     

Performance of aerobic digestion at different sludge solid levels and operation patterns

Laboratory batch and semi-continuous experiments were carried out at 20°C on the aerobic digestion of primary sludges and waste secondary activated sludges. Solids concentrations up to 60.000 mg l⁻¹ (6%) for primary sludges and 20.000 mg l⁻¹ (2%) for waste secondary activated sludges, were employed. It was found that aerobic digestion of more concentrated sludges was associated with slower solids degradation rates, but in the studied range of concentrations, more concentrated sludges yielded a higher mass of volatile suspended solids decomposed per unit digester volume per day. For the primary and secondary sludges with the same volatile suspended solids concentration, the amounts of volatile suspended solids decomposed per unit digester volume per day were closely comparable.The results from batch digestion experiments proved not to be directly applicable to the design of continuous flow aerobic digesters. It was also demonstrated that the treatment of a sludge with a higher solids concentration could be an effective means of utilizing the digester volume while obtaining a reasonably well stabilized product sludge.     

(AO)2-SBBR反硝化除磷工艺处理低碳城市污水

低碳源浓度城市污水的脱氮除磷一直是个难题，为此在AO-SBBR工艺中引入一个缺氧段而形成（AO）2-SBBR工艺，研究了AO-SBBR和（AO）2-SBBR对低碳源浓度城市污水中氮、磷的去除效果。试验结果表明：在进水BOD5／TN=3、BOD5／TP=17的情况下，（AO）2-SB．BR工艺比AO-SBBR工艺具有更好的同步脱氮除磷效果，对总磷的去除率达到了79．8％，对总氮的去除率从25．83％提高到51．26％，出水水质达到了《城镇污水处理厂污染物排放标准》的一级标准。该工艺有效解决了低碳源浓度城市污水在同步脱氮除磷过程中有机物不足的问题，并在单一反应器中实现了反硝化除磷菌的增殖过程，反硝化除磷菌占聚磷菌的比例从14．82％增长到63．04％；反硝化除磷菌能够以低浓度的亚硝酸盐氮作为电子受体进行缺氧吸磷，如亚硝酸盐氮〉10mg／L则会抑制反硝化除磷菌的活性，而且这种抑制作用并不是瞬时的，至少要持续一段时间其活性才能恢复。