COD对生物除磷颗粒污泥稳定性影响研究

颗粒污泥稳定性是影响其应用的主要因素之一.以SBR中成熟的生物除磷颗粒污泥为研究对象,探讨进水COD浓度对系统稳定性的影响.结果表明,当进水COD浓度由300 mg/L逐渐升高到500 mg/L时,磷去除率由93%降低到88%;当进水COD浓度在400 mg/L以下时,污泥的最大比释磷速率和比吸磷速率分别为45.2 m...     

Improved computational model (AQUIFAS) for activated sludge, integrated fixed-film activated sludge, and moving-bed biofilm reactor systems, part III: analysis and verification

Research was undertaken to analyze and verify a model that can be applied to activated sludge, integrated fixed-film activated sludge (IFAS), and moving-bed biofilm reactor (MBBR) systems. The model embeds a biofilm model into a multicell activated sludge model. The advantage of such a model is that it eliminates the need to run separate computations for a plant being retrofitted from activated sludge to IFAS or MBBR. The biofilm flux rates for organics, nutrients, and biomass can be computed by two methods-a semi-empirical model of the biofilm that is relatively simpler, or a diffusional model of the biofilm that is computationally intensive. Biofilm support media can be incorporated to the anoxic and aerobic cells, but not the anaerobic cells. The model can be run for steady-state and dynamic simulations. The model was able to predict the changes in nitrification and denitrification at both pilot- and full-scale facilities. The semi-empirical and diffusional models of the biofilm were both used to evaluate the biofilm flux rates for media at different locations. The biofilm diffusional model was used to compute the biofilm thickness and growth, substrate concentrations, volatile suspended solids (VSS) concentration, and fraction of nitrifiers in each layer inside the biofilm. Following calibration, both models provided similar effluent results for reactor mixed liquor VSS and mixed liquor suspended solids and for the effluent organics, nitrogen forms, and phosphorus concentrations. While the semi-empirical model was quicker to run, the diffusional model provided additional information on biofilm thickness, quantity of growth in the biofilm, and substrate profiles inside the biofilm.     

Influence of chemical oxygen demand/total Kjeldahl nitrogen ratio and sludge age on nitrification of nitrogenous wastewater.

Four laboratory-scale biological nitrification units (influent total Kjeldahl nitrogen [TKN] = 1002 to 1062 mg/L) were operated at chemical oxygen demand (COD)/TKN ratios of approximately 0.5, 1.0,15, and 2.0 and at three different sludge ages of 30, 20, and 10 days to study the influence of COD/TKN, sludge age, COD loading, and TKN loading on nitrification and nitrifiers. Percent nitrification was found to increase with decreases in COD/TKN and increases in sludge age. The average nitrifier concentration increased from 460 mg/L at a COD/TKN of 2.22 and a sludge age of 10 days to 706 mg/L at a COD/TKN of 0.676 and a sludge age of 30 days. The nitrifier fraction was found to be higher at a lower COD/TKN and lower at a higher COD/TKN. The nitrifier fraction increased with the decrease in sludge age and COD loadings and the increase in TKN loadings. The effect of sludge age on the nitrifier fraction was amplified at a COD/ TKN of approximately 0.5 rather than at approximately 2.0. The nitrification rate (kilograms TKN oxidized per kilograms nitrifiers per day) was shown to be dependent on COD/TKN and sludge age. The activity performed by Nitrobacter was affected at all COD/TKN ratios studied as well as at a sludge age of 10 days. This was manifested by the accumulation of high levels of nitrite-nitrogen in the nitrified effluent. The presence of heterotrophs did not affect nitrification rates and the growth of nitrifiers, which were found to be beneficial. High sludge age and COD loadings resulted in a higher sludge volume index of more than 200 mL/g mixed liquor suspended solids. Microscopic examination showed filamentous structure of sludge under these conditions. It is concluded from the investigations that a sludge age of 30 days and a COD/TKN of approximately 1.0 are optimal to yield maximum nitrification and nitrifier growth rates for treating high-strength nitrogenous wastewater.     

铬离子对SBR工艺活性污泥毒性作用研究

针对重金属铬离子对SBR工艺系统中活性污泥的毒性作用,通过检测不同初始污泥容积指数(SVI)下SBR工艺活性污泥在不同铬负荷下的COD值、挥发性污泥浓度以及受铬离子影响的污泥容积指数(SVI),研究重金属铬离子对活性污泥的毒性作用以及对SBR工艺系统处理污水的影响。研究表明,重金属铬离子会导致SBR工艺系统出水COD升高;将铬离子对活性污泥的毒性作用按照挥发性污泥(MLVSS)铬负荷可划分为耐受范围、非耐受范围、细胞失活范围以及细胞分解范围。耐受范围铬负荷低于约30 mg Cr3+/gMLVSS,此范围内铬离子对于活性污泥的毒性作用不大,不致于导致系统出水水质变差;非耐受范围铬负荷在约30~65 mg Cr3+/g MLVSS,在铬离子作用下系统出水COD值明显高于对照系统;细胞失活范围铬负荷在约70~100 mg Cr3+/gMLVSS范围内,SVI大幅下降,微生物部份死亡和失活,出水COD尽管有一些下降,但与进水COD相比差不了多少;细胞分解范围铬负荷在约100 mg Cr3+/gMLVSS以上,微生物大量死亡,部分死亡细胞分解,系统出水COD值因微生物的死亡分解而超出进水COD值,受铬离子影响的系统SVI值大幅度降低。     

AOAB工艺处理难降解混合化工污水的挂膜启动

采用AOAB(水解酸化A1+生物接触氧化O+深度水解酸化A2+曝气生物滤池BAF)工艺处理难降解混合化工污水,重点研究工艺挂膜方式和生物膜的驯化。结果表明,采用分段连续式挂膜法进行反应器挂膜,20 d即可完成快速挂膜启动;采用分阶段同步培养驯化法驯化生物膜,30 d内可完成高浓度多组分混合化工污水进水的驯化,最终进水COD 1 456 mg/L,出水COD 324 mg/L,总去除率76.85%,驯化效果显著;整个工艺对COD的降解主要集中在生物接触氧化池和曝气生物滤池,驯化期间生物接触氧化池去除率稳定在40%左右,曝气生物滤池去除率稳定在50%以上。同时,通过对比一段水解酸化和深度水解酸化的VFA(挥发性脂肪酸)产出,表明在高有机负荷进水时,一段水解酸化降解大分子有机物的能力有限,但这些有机物可通过二段水解酸化再次降解,由此体现了AOAB工艺在处理多组分混合型的难降解化工污水的优势。     

Specific resistance to filtration of biomass from membrane bioreactor reactor and activated sludge: effects of exocellular polymeric substances and dispersed microorganisms.

This study investigates the effect of dispersed microorganisms and exocellular polymeric substances on biomass dewaterability. Specific resistance to filtration (SRF) was measured for biomass from a membrane bioreactor and a completely mixed activated sludge system. Both laboratory-scale reactors were fed with synthetic wastewater and operated at a high food-to-microorganism ratio (F/M) (1 to 11 kilograms chemical oxygen demand per kilogram mixed liquor volatile suspended solids per day [kgCOD/(kg MLVSS.d)]) and short solids retention times (0.25 to 5 d). The SRF values were affected by strong interactions of three parameters: (1) the mixed liquor suspended solids concentration, (2) the amount of dispersed microorganisms, and (3) the exocellular polymeric substances (EPS) concentration. At F/M smaller than 2 kg COD/(kg MLSS.d) and mixed liquor suspended solids (MLSS) concentration higher than 2000 mg/L, increasing amount of dispersed microorganisms in the biomass yielded higher SRF values. However, at high F/M (> 5 kg COD/kg MLSS.d) and low MLSS concentrations (< 600 mg/L), lower EPS concentrations resulted in slightly smaller SRF values, even though the amount of dispersed microorganisms in the biomass was much higher. Thus, at low MLSS concentrations, EPS concentrations rather than the amount of dispersed microorganisms tend to control SRF.     

The effect of wastewater cations on activated sludge characteristics: effects of aluminum and iron in floc.

Wastewater samples collected from seven wastewater treatment plants (WWTPs) were characterized to assess the impacts of wastewater cations on the activated sludge process. The cations included in this study were sodium (Na+), potassium, ammonium, calcium, magnesium, aluminum (Al), and iron (Fe). Among the selected cations, Al and Fe were of most interest to this study because their role in bioflocculation has not been extensively studied and remains largely unknown. The data showed that WWTPs contained highly varying concentrations of Na+, Al, and Fe in the wastewater and that these cations were responsible for differences between WWTPs as to sludge dewatering rates and effluent quality. In general, a high influent Na+ concentration caused poor sludge dewatering and effluent characteristics. However, when sufficient Al and Fe were present in floc, the deleterious effects of Na+ were offset. The data associated with Al further revealed that waste activated sludge with low Al contained high concentrations of soluble and colloidal biopolymer (protein + polysaccharide), resulting in a high effluent chemical oxygen demand, high conditioning chemical requirements, and poor sludge dewatering properties. These results suggest that Al will improve activated sludge effluent quality by scavenging organic compounds from solution and binding them to floc.     

Removal of a broad range of surfactants from municipal wastewater--comparison between membrane bioreactor and conventional activated sludge treatment

Elimination of alkylphenol ethoxylates (APEO) and their degradation products (alkylphenols and alkylphenoxy carboxylates), as well as linear alkylbenzene sulfonates (LAS) and coconut diethanol amides (CDEA), was studied in a pilot plant membrane bioreactor (MBR) working in parallel to a full-scale wastewater treatment plant (WWTP) using conventional activated sludge (CAS). In the CAS system 87% of parent long ethoxy chain NPEOs were eliminated, but their decomposition yielded persistent acidic and neutral metabolites which were poorly removed. The elimination of short ethoxy chain NPEOs (NP(1)EO and NP(2)EO) averaged 50%, whereas nonylphenoxy carboxylates (NPECs) showed an increase in concentrations with respect to the ones measured in influent samples. Nonylphenol (NP) was the only nonylphenolic compound efficiently removed (96%) in the CAS treatment. On the other hand, MBR showed good performance in removing nonylphenolic compounds with an overall elimination of 94% for the total pool of NPEO derived compounds (in comparison of 54%-overall elimination in the CAS). The elimination of individual compounds in the MBR was as follows: 97% for parent, long ethoxy chain NPEOs, 90% for short ethoxy chain NPEOs, 73% for NPECs, and 96% for NP. Consequently, the residual concentrations were in the low mug/l level or below it. LAS and CDEA showed similar elimination in the both wastewater treatment systems that were investigated, and no significant differences were observed between the two treatment processes. Nevertheless, for all studied compounds the MBR effluent concentrations were consistently lower and independent of the influent concentrations. Additionally, MBR effluent quality in terms of chemical oxygen demand (COD), NH(4)(+) concentration and total suspended solids (TSS) was always superior to the ones of the CAS and also independent of the influent quality, which demonstrates high potential of MBRs in the treatment of municipal wastewaters.     

摇动床生物膜反应器和活性污泥法组合技术处理高浓度有机废水的研究

利用摇动床生物膜反应器(简称摇动床)技术具有的容积负荷高与污泥产量低的优点,在普通活性污泥池的前部填充高性能丙烯酸树脂纤维(Biofringe)填料,研究了摇动床和活性污泥法组合技术处理高浓度有机废水的有效性。结果表明,该组合技术具有很强的有机物去除能力,当进水COD平均质量浓度由1500mg/L上升到2514mg/L时,出水COD的平均去除率基本保持在96%以上;整个运行阶段的出水COD浓度均满足《污水综合排放标准》(GB8978—1996)的二级标准;当进水NH4+-N浓度增加时,NH4+-N的去除率由99.7%降低到76.5%,但是在试验运行的整个阶段,摇动床和活性污泥法组合技术系统都表现出较强的硝化能力;活性污泥池中最高的混合液悬浮固体(MLSS)质量浓度为10625mg/L,最高MLSS约为普通活性污泥法的4倍;运行结束后的污泥产率为0.186,污泥产率仅为普通活性污泥法的50%左右。     

Hydraulic residence time effects on performance of an activated sludge unit treating wastewater containing dichlorophenol.

Wastewaters containing chlorophenol compounds are difficult to treat by biological means because of the toxic effects of those compounds on microorganisms. To investigate the adverse effects of chlorophenols on microorganisms, synthetic wastewater containing 2,4 dichlorophenol (DCP) was biologically treated in an activated sludge unit at different hydraulic residence times (HRTs) between 5 and 40 hours, whereas the feed chemical oxygen demand (COD), DCP concentrations, and sludge age were kept constant at 2500 +/- 50 mg/L, 150 mg/L, and 20 days, respectively. The resazurin method based on dehydrogenase activity was used for assessment of the feed and effluent wastewater toxicity. Percent COD, DCP, and toxicity removals increased, and the effluent COD, DCP, and toxicity levels decreased with increasing HRT. Biomass concentration in the aeration tank increased with increasing HRT because of low levels of DCP at high HRT levels, resulting in high COD, DCP, and toxicity removals. The sludge volume index decreased with increasing HRT, yielding well-settling organisms as a result of low levels of toxicity and high concentrations of active cells. Percent DCP and COD removals decreased with increasing specific DCP loading rate. The rates of DCP and COD removals showed a maximum at a low DCP concentration of 6 mg/L in the aeration tank, corresponding to a 25-hour HRT.     

4-硝基酚的污泥减量化作用及对污泥性质的影响

为了有效减少活性污泥法中剩余污泥的产生,采用解偶联剂4-硝基酚对活性污泥工艺中的剩余污泥进行减量化研究。研究了4-硝基酚对污泥的增长速率、基质去除率以及污泥性质的影响。结果表明:4-硝基酚对污泥的减量化作用明显,在对微生物解偶联的过程中并不影响微生物对基质的利用能力;对出水中的氨氮影响甚小,总氮、总磷浓度有轻微的升高。4-硝基酚能够刺激污泥中微生物的活性,比耗氧速率增加,促进能量解偶联,从而降低污泥产率。4-硝基酚使污泥中微生物的群落结构发生了轻微的变化,但对污泥的松散程度和絮凝沉降性能影响甚小。     

SBR法处理豆制品废水工艺条件的研究

用SBR法处理豆制品废水的试验表明,该系统具有较好的抗负荷冲击能力,进水COD在300～2000 mg/L之间变化,对系统不造成任何影响;考察了曝气时间、曝气量和污泥浓度等对去除效果的影响,试验结果表明,曝气时间和曝气量对处理效果影响很大,确定该反应系统最佳曝气时间是8 h,适宜的曝气量是800 L/h,而污泥浓度控制在4000 mg/L左右时,处理效率最高,采用进水顶出水的排水方式是可行的,确定系统的最佳排水比是3/5.厌氧段的插入可以减少剩余污泥的产量.     

Petroleum refinery stripped sour water treatment using the activated sludge process

A pilot study was performed over 91 days to determine if the activated sludge process could treat a segregated stripped sour water (SSW) stream from a petroleum refinery. The study was performed in two periods. The first period was terminated after 19 days, as a result of excessive sludge bulking. The elimination of sludge bulking during the 70-day second period is attributed to operational changes, which included aerating the influent to oxidize reduced sulfur, adjusting the influent pH, and adding micronutrients to satisfy biological requirements. The pilot plant provided a chemical oxygen demand (COD) removal of up to 93%. Nitrification was achieved, with effluent ammonia values < 1 mg-N/L. These results indicate that direct treatment of SSW with the activated sludge process is possible and has direct application to full-scale petroleum refinery wastewater plant upgrades.     

倒置A~2/O-MBR(平板膜)处理城市污水的中试研究

针对城市生活污水,研究了两点进水倒置A2/O-MBR(平板膜)系统(以下简称系统)对COD、NH+4-N、TN、TP、出水SS影响。结果表明,该系统对COD、NH+4-N具有较高的去除率,出水符合GB18918-2002中一级A标准;当混合液回流比为200%时,系统出水TN浓度小于15 mg/L;正常排泥后,系统对TP的去除率达83%左右;平板膜破损会导致出水SS、COD会受到影响。膜对COD、TP、SS有直接截留作用,由于系统出水几乎没有固体损失,可以精确控制污泥龄,有利于世代周期较长的硝化菌和反硝化菌生长;系统中的污泥浓度可以提高至15 000 mg/L,此时,即使进水量提高0.5倍,出水水质仍保持良好。     

Considerations about the enantioselective transformation of polycyclic musks in wastewater, treated wastewater and sewage sludge and analysis of their fate in a sequencing batch reactor plant

The present work consists of two distinct parts: in the first part enantioselective GC was used to separate the different enantiomeric/diastereomeric polycyclic musks, PCMs (HHCB, AHTN, AHDI, ATII and DPMI) including the main transformation product of HHCB, HHCB-lactone, in wastewater and sewage sludge. After optimization all PCMs were resolved on a cyclodextrin containing Rt-BDEXcst capillary GC column. Enantiomeric ratios of PCMs in a technical mixture were determined and compared to those obtained from enantioselective separation of wastewater and sewage sludge samples. In general, enantiomeric ratios were similar for most materials in influent, effluent and stabilized sewage sludge. However, the ratios for HHCB, AHDI and particularly ATII suggest some stereospecific removal of these compounds. In the second part, a field study was conducted on a wastewater treatment plant comprising a sequencing batch reactor. Concentrations of HHCB, AHTN, ADBI, AHDI, ATII, DPMI and HHCB-lactone were determined by non-enantioselective GC in daily samples of influent, effluent and activated sludge during one week. Mean concentrations in influent were 6900 and 1520 ng/l for HHCB and AHTN, respectively. The other PCMs exhibited contents 200 ng/l. Mean percent removal was between 61% (AHDI) and 87% (HHCB) resulting in mean effluent concentrations below 860 ng/l. HHCB-lactone concentration increased during wastewater treatment with a mean in the influent of 430 ng/l and in the effluent of 900 ng/l, respectively, indicating a degradation of HHCB.     

Biological treatment of a synthetic gold milling effluent

This paper reports on biological sludge acclimatisation and the results concerning the removal of free cyanide, thiocyanate and metallocyanides (copper, iron and zinc) from a synthetic gold milling effluent. The experiments were carried out in a continuous bench-scale bioreactor, and the experimental set-up consisted of two identical units, one of which served as control. The acclimatisation of the biomass was based on a stepwise procedure, in which the proportion of synthetic solution in the influent was gradually increased. The reactors were fed with a mixture of synthetic effluent and sewage, and the treatment efficiency was evaluated through the monitoring of the following parameters: chemical oxygen demand (COD), free cyanide, thiocyanate, copper, iron and zinc concentrations. A well adapted microbial consortium was obtained at the end of the acclimatisation period, which was able to remove more than 95% of free cyanide, thiocyanate, copper and zinc, originally found in the influent. These removal efficiencies were obtained when the reactor was operated with a hydraulic retention time (HRT) of about 8 h. The performance results of experiments carried out with lower HRT (5 h) and higher dissolved oxygen (DO) concentration (6.5 mg litre(-1)) are also presented and discussed in this study.     

Fate of Terpene Compounds in Activated Sludge Wastewater Treatment Systems

ABSTRACT

Terpene-based cleaners are being widely used in industrial cleaning formulations because of their ability to replace suspected ozone-depleting chemicals such as 1,1,1-trichloroethane and 1,1,2-trichloro-1,2,2-trifluoroethane (CFC-113). Substitution of chlorinated solvents with ter-pene-based cleaners, however, is expected to result in increased discharges to wastewater from industrial operations. A pilot-scale study was conducted at the U.S. Environmental Protection Agency's (EPA) Test & Evaluation Facility in Cincinnati, OH, to quantify the fate of specific terpene compounds in the activated sludge wastewater treatment process. Biodegradation rates of terpenes were estimated from the difference between the influent terpene mass flow rates and the amounts volatilized to air, partitioned to waste sludge, and passed through the treatment process unchanged. Any chemical transformation of the terpene compounds studied was attributed to biodegradation.

Analytical methods were developed to determine ter-pene concentrations in aqueous and gaseous media. The fate of two common terpene compounds (d-limonene and terpinolene) were evaluated in three identical pilot-scale systems: (1) a system with a high target spike range (2–10 mg/L), (2) a system with a low target spike range (0.5–2 mg/L), and (3) a control system (no spike).

The study showed that the primary removal mechanism for the terpene compounds in the activated sludge process is biodegradation. Typically, greater than 90% of the mass of terpenes entering the aeration basin of the activated sludge process biodegrades to other compounds; volatilization from the reaction basin accounts for less than 10%, while loss to waste activated sludge and the secondary clarifier effluent accounts for less than 1%.     

SBR法处理豆制品废水工艺条件的研究

用SBR法处理豆制品废水的试验表明，该系统具有较好的抗负荷冲击能力，进水COD在300—2000mg／L之间变化，对系统不造成任何影响；考察了曝气时间、曝气量和污泥浓度等对去除效果的影响，试验结果表明，曝气时间和曝气量对处理效果影响很大。确定该反应系统最佳曝气时间是8h，适宜的曝气量是800L／h，而污泥浓度控制在4000mg／L左右时，处理效率最高，采用进水顶出水的排水方式是可行的，确定系统的最佳排水比是3／5。厌氧段的插入可以减少剩余污泥的产量。     

Effect of mixed liquor suspended solids concentration on the biodegradation of nitrilotriacetic acid in the activated sludge process

The biodegradation of nitrilotriacetic acid in laboratory simulations of the activated sludge process has been studied at two different concentrations of mixed liquor suspended solids. Responses to changes in the influent nitrilotriacetic acid concentration such as those which might be associated with a “wash day” have been examined.     

Investigation of Cr(VI) reduction in continuous-flow activated sludge systems

The aim of this research was to investigate hexavalent chromium, Cr(VI), reduction by activated sludge and to evaluate the use of continuous-flow activated sludge systems for the treatment of Cr(VI)-containing wastewater. Three series of experiments were conducted using two parallel lab-scale activated sludge systems. During the first experiment, one system was used as a control, while the other received Cr(VI) concentrations equal to 0.5, 1, 3 and 5mg l(-1). For all concentrations added, approximately 40% of the added Cr(VI) was removed during the activated sludge process. Determination of chromium species in the dissolved and particulate phase revealed that the removed Cr(VI) was sorbed by the activated sludge flocs mainly as trivalent chromium, Cr(III), while the residual chromium in the dissolved phase was mainly detected as Cr(VI). Activated sludge ability to reduce Cr(VI) was independent of the acclimatization of biomass to Cr(VI) and it was not affected by the toxic effect of Cr(VI) on autotrophic and heterotrophic microorganisms. During the second experiment, both systems were operated under two different hydraulic residence time (theta equal to 20 and 28h) and three different initial organic substrate concentration (COD equal to 300, 150 and 0mg l(-1)). Cr(VI) reduction was favored by an increase of theta, while it was limited by influent COD concentration. Finally, at the last experiment the effect of anoxic and anaerobic reactors on Cr(VI) reduction was investigated. It was observed that the use of an anoxic zone or an anaerobic-anoxic zone ahead of the aerobic reactor favored Cr(VI) reduction, increasing mean percentage Cr(VI) reduction to almost 80%.