曝气生物滤池去除有机物及硝化氨氮的影响因素研究

采用以陶粒为填料的曝气生物滤池(BAF)处理低浓度生活污水,研究在气水比一定的条件下,水力负荷、有机负荷及氨氮负荷对BAF去除有机物及硝化氨氮的性能的影响.研究结果表明,当试验进水COD为105.8～156.6 mg/L,气水比为3:1的条件下,降解有机物的最佳水力负荷为1.35～1.68 m3/(m2·h),COD平均去除率为86.3%.氨氮负荷是影响反应器硝化性能的直接因素.当水力负荷为1.05 m3/(m2·h),平均进水COD为106.1 mg/L时,若使出水氨氮低于15 mg/L,则反应器能承受的最大进水氨氮负荷为0.5 kg/(m3·d)左右.并确立了相应的反应器动力学模型.     

内循环厌氧反应器处理养猪场污水基质降解动力学模型研究

依据对IC反应器有机物降解特性的分析,以及对其精细处理区和污泥床区水力流态分别作推流和全混流处理,基质降解速率与微生物浓度之间按一级反应处理的基础上,建立了IC反应器基质降解动力学理论模型.并根据IC反应器处理养猪场污水的试验结果,确定出了反应器在平均温度为(33±0.5)℃条件下污泥床区和精细处理区内基质降解动力学模型.     

A/O一体化曝气生物滤池降解酱油废水的研究

针对组分复杂、色度较高的酱油废水,采用A/O一体化曝气生物滤池进行处理,研究了该反应器处理酱油废水的运行参数及降解动力学.结果表明:采用以废弃物煤渣为主的混合填料,能有效去除废水中的有机物和色度.当水力负荷为1.12 m3/(m2·h),容积负荷为0.15～0.43 kg COD/(m3·d)的条件下,反应器的COD去除率能维持在75%～85%之间,色度去除率均在80%以上,最高达到了93.3%;当容积负荷小于0.27 kg COD/(m3·d)时,出水的各项指标能达到(GB8978-1996)的一级排放标准.根据试验结果,反应器O段的降解动力学可表达为Se/S0=exp(-1.0125H).     

水力负荷对厌氧氨氧化反应器运行影响的研究

采用一套有效容积为4.46 L的UASB-ANAMMOX反应器,通过对水力负荷进行3个阶段的调节,研究水力停留时间对ANAMMOX反应器处理效果的影响.3个阶段的水力负荷分别为0.20～0.25、0.38～0.43、0.16～0.20 L/(Ld).在试验过程中,水力负荷的冲击对NH 4-N、NO-2-N的去除率影响明显.其中水力负荷为0.20～0.25 L/(L·d)时,NH 4-N、NO-2-N去除率都能达到99%以上;当水力负荷为0.38～0.43 L/(L·d)时,NH 4-N、NO-2-N去除率分别降至64%和62%;当水力负荷为0.16～0.20 L/(L·d)时,NH 4-N、NO-2-N去除率立刻分别回升至94%和97%.ANAMMOX反应过程中,NO-2-N和NH 4-N的去除量比值基本在1.3∶1.0左右变化,ANAMMOX反应的优势菌种代谢在运行过程中会将一部分NO-2-N转化为NO-3-N,水力负荷的改变对NO-3-N的出水浓度影响不大;但NO-3-N日生成量与水力负荷的大小成正比.试验表明,UASB-ANAMMOX反应器对水力负荷冲击有较强的抵抗力,但是仍会造成一定量的ANAMMOX反应的优势菌流失,使该反应器在短时间内不能恢复最佳的去除效果.     

特殊工况下船舶生活污水处理的试验研究

采用厌氧复合床反应器与接触氧化、接触沉淀相结合的工艺,针对实船条件下可能出现的重启动、倾斜、海水及淡水海水交替冲洗厕所和水力负荷增加等情况,进行了特殊工况下船舶生活污水处理的试验研究.结果表明,该组合工艺在设计条件下(HRT为5 h)重启动速度较快,可用于海水冲厕所产生的高盐度污水处理,耐受淡水海水交替变化的盐度冲击负荷变化能力较强,具有一定的水力负荷增加潜力,并且不受倾斜影响.     

旋转流厌氧附着膜膨胀床运行及水力流态研究

试验以树脂为载体,用自行设计的旋转流厌氧附着膜嘭胀床处理高浓度有机废水.经过启动、中等负荷稳定运行及高负荷稳定运行等阶段,成功地培养出高效生物膜颗粒,最高有机负荷达46.4 kg/(m3·d).相应的COD去除率大于80%.在反应器运行过程中采用脉冲示踪法,以LiCl作示踪剂,对反应器的水力流态规律进行了系统的试验研究.研究表明,水力上升流速及气体负荷是影响反应器容积利用率及反应器内固液两相混合程度的重要因素.     

膨胀颗粒污泥床反应器启动过程中颗粒污泥性质变化研究

采用小试规模的膨胀颗粒污泥床(EGSB)反应器,考察其启动规律及运行特点.在60 d内EGSB反应器的COD容积负荷达到12 kg/(m3·d),COD去除率保持在95%以上.试验中对不同水力负荷下污泥床状态进行了分析.结果表明,将水力负荷控制在1.0 m3/(m2·h)以上,可以确保污泥颗粒化的进行及EGSB反应器的稳定,否则易发生沟流、活塞式漂浮等污泥床异常现象.同时,对颗粒污泥性质及微生物相变化进行了跟踪分析.随着运行条件的改变,由上流式厌氧污泥床(UASB)反应器接种的污泥结构、性能和微生物群落都在不断发生变化.最终得到的颗粒污泥结构密实,沉降速率为38.8～64.6 m/h,比产甲烷活性达到314.25 mL/(g·d),内部微生物相丰富,各菌种呈混杂分布.     

容积负荷对ANAMMOX生物滤池脱氮效能的影响及其基质动力学

采用2套启动成功的上向流厌氧氨氧化（ANAMMOX）生物滤柱,通过调节进水NaNO₂和（NH₄）₂SO₄ 的浓度负荷及水力负荷,改变进水容积负荷,探讨容积负荷对ANAMMOX生物滤柱脱氮效能的影响及其动力学模型。结果表明,滤速恒定条件下,通过提高进水基质浓度来提高进水TN容积负荷,其容积负荷去除动力学过程符合Monod-Haldane基质抑制模型。进水NH₄⁺-N与NO₂^--N浓度分别低于100 mg/L和133 mg/L时,反应器脱氮效果不受明显影响,TN容积去除负荷可达4.21 kg/（m³·d）,TN去除率可达80%以上。进水基质浓度恒定条件下,通过提高滤速来提高进水TN容积负荷,其容积负荷去除动力学过程符合零级动力学方程。不受基质浓度抑制的条件下,滤速为3.0 m/h、进水容积负荷为8.82 kg/（m³·d）时,反应器总氮容积负荷去除量可达7.15 kg/（m³·d）,总氮去除率可达81.1%。     

微污染水源水生物处理工艺中IAL-CHS与三相流化床的初步比较

初步比较气升式内循环蜂窝陶瓷反应器(IAL-CHS)和内循环三相流化床反应器(ITFB)对微污染水源水进行生物预处理的效果。IAL-CHS反应器比ITFB反应器挂膜启动速度快,但是在挂膜期承受冲击负荷能力较ITFB反应器差。在进水相同条件下,两者所能达到的最小水力停留时间、最大体积负荷和容积负荷相差不大,但是ITFB反应器的曝气强度却为IAL-CHS反应器的3.33倍,并且比IAL-CHS反应器出水SS高,浊度去除率低,单位载体的生物量及活性生物量小。     

高基质浓度下厌氧氨氧化反应器的启动过程

采用3套厌氧序批式生物膜反应器,研究了高基质浓度对厌氧氨氧化反应器启动过程的影响。经过50 d左右培养,3个反应器氮容积去除负荷均达到0.23 kg N/(m3.d)。但是随着氮容积负荷的提高,反应器内pH也随之升高,最终超过了厌氧氨氧化菌最适生长条件,3个反应器脱氮效果逐渐下降。然后分别通过降低浓度、延长水力停留时间的方式对其脱氮效能进行恢复性研究。结果表明高基质浓度不利于厌氧氨氧化反应器脱氮能力的增强。采用低基质浓度的方式提高反应器氮容积去除负荷时,脱氮效能不仅得到了恢复,而且能够提高到0.45 kg N/(m3.d)。说明低基质难度比高基质浓度更有利于厌氧氨氧化脱氮效能的提高。     

2种不同填料曝气生物滤池处理生活污水的经验模型

对分别装有火山岩和陶粒填料的2套平行运行的曝气生物滤池,在不同的进水负荷下进行生活污水的试验研究,结果表明火山岩的溶解性COD(SCOD)去除效果要优于陶粒。同时,根据大量试验数据针对2个反应器进出水SCOD随反应器高度的变化关系,建立一套经验模型。推算出不同水力负荷下的经验模型常数n和K值,结果表明模型的预测值与实测值是相吻合的,该模型可作为设计者和运行者的参考依据。     

改进型曝气生物滤池对生活污水氮去除的影响

采用下向流中部曝气的运行方式,对生活污水进行了处理,考察了气水比、有机负荷对生物滤池的去除效果及其沿程生化特性。结果表明:水力停留时间为8 h,气水比为10∶1条件下可获得最佳的处理效果,COD、TN和NH4+-N的平均去除率分别为92.5%、48.6%和69.4%。进水有机负荷增加,COD和NH4+-N的去除率下降,TN的去除率可达60.5%。结合理论分析,对脱氮性能进行了探讨。     

One-at-a-time sensitivity analysis of pollutant loadings to subsurface properties for the assessment of soil and groundwater pollution potential

Chemical leak was numerically simulated for four chemical substances: benzene (light non-aqueous phase liquid (NAPL)), tetrachloroethylene (dense NAPL), phenol (soluble in water), and pentachlorophenol (white crystalline solid) in a hypothetical subsurface leak situation using a multiphase compositional transport model. One metric ton of chemical substances was assumed to leak at a point 3.51 m above the water table in a homogeneous unconfined aquifer which had the depth to water table of 7.135 m, the hydraulic gradient of 0.00097, the recharge rate of 0.7 mm/day, and the permeability of 2.92?×?10^?10 m². For comparison, surface spill scenarios, which had a long pathway from source to the water table, were simulated. Using the model results, point-source pollutant loadings to soil and groundwater were calculated by multiplying mass, impact area, and duration above and below the water table respectively. Their sensitivity to subsurface properties (depth to water table, recharge rate, porosity, organic carbon content, decay rate, hydraulic gradient, capillary pressure, relative permeability, permeability) was analyzed, with changing each parameter within acceptable ranges. The study result showed that the pollutant loading to groundwater was more sensitive to the subsurface properties than the pollutant loading to soil. Decay rate, groundwater depth, hydraulic gradient and porosity were influential to pollutant loadings. The impact of influential parameters on pollutant loadings was nonlinear. The dominant subsurface properties of pollution loadings (e.g., decay rate, groundwater depth, hydraulic gradient, and porosity for groundwater) also affect the vulnerability, and the subsurface pollutant loadings defined in this study are dependent on chemical properties as well, which indicates that the influential hydrogeological and physicochemical parameters to pollutant loadings can be used for pollution potential assessment. The contribution of this work is the suggestion that the sensitivity of pollutant loadings can be used for pollution potential assessment. Soil and groundwater pollution potential of chemicals are discussed altogether for leak scenarios. A physics-based model is used to understand the impact of subsurface properties on the fate and transport of chemicals above and below the water table, and consequently their impact on the pollutant loading to soil and groundwater.

     

铁炭微电池电解填充流化床反应器水力学行为研究

本文提出了一种新型的铁炭微电池电解反应器———填充流化床反应器 ,并对该反应器的水力学行为进行了研究。通过床层压降法测定临界流化气速 ,建立了关于临界流化气速Uc 的经验关联式 :Uc=0 .0 15 6C0 .2 7Vt0 .14 H0 .31。通过脉冲示踪物信号法测得停留时间分布密度函数E(t) ,结果表明该反应器水力混合特性接近于完全混合反应器     

中试螺旋式自循环厌氧反应器处理安乃近制药废水的稳定性能简

以制药废水实验了50 m³螺旋式厌氧反应器（SPAC反应器）的稳定性。采用Augmented Dickey-Fuller（ADF）单位根检验表明,螺旋式反应器具有良好的启动和运行稳定性。负荷冲击实验显示,SPAC反应器具有较好的耐浓度冲击能力和耐水力冲击能力,所能耐受的最大浓度冲击强度大于60 000 （mg·h）/L（进水浓度提升2倍）,所能耐受的最大水力冲击强度为300（m³·h）/d（进水流量提升50%）。SPAC反应器还具备受扰恢复能力。在反应液pH低于5.74,出水浓度、COD去除率和容积COD去除速率（VRR）分别为3 500 mg/L、22.30%和2.52 kg/（m³·d）的工况下,经过30 d恢复,出水浓度、COD去除率和VRR的恢复程度达到80%~90%。     

Fluidized zero valent iron bed reactor for nitrate removal

A fluidized zero valent iron (ZVI) reactor is examined for nitrate reduction. Using the system, the pH of solution can be maintained at optimal conditions for rapid nitrate reduction. For hydraulic retention times of 15 min, the nitrate reduction efficiency increases with increasing ZVI dosage. At ZVI loadings of 33 gl-1, results indicate that the nitrate removal efficiency increases from less than 13% for systems without pH control to more than 92% for systems operated at pH of 4.0. By maintaining pH at 4.0, we are able to decrease the hydraulic retention time to 3 min and still achieve more than 87% nitrate reduction. The recovery of total nitrogen added as nitrate, ammonium, and nitrite was less than 50% for the system operated at pH4.0, and was close to 100% for a system without pH control. The possibility of nitrate and ammonium adsorption onto iron corrosion products was ruled out by studying the behavior of their adsorption onto freshly hydrous ferric oxide at variable pH. Results indicate the probable formation of nitrogen gas species during reaction in pH4.0.     

生物膜反应器连续处理餐饮废水

用生物膜反应器连续处理餐水能有效降低废水中的ＢＯＤ及ＣＯＤ浓度。研究了水力停留时间对有机物去除率的影响,结果表明当水力停留时间大于７．８ｈ时,废水的ＣＯＤ,ＢＯＤ及ＴＳＳ的去除率均高于９０％。实验操作时,水力停留时间应略大于５．７ｈ。     

Bio-reduction of N-nitrosodimethylamine (NDMA) using a hydrogen-based membrane biofilm reactor

N-Nitrosodimethylamine (NDMA) is a disinfection by-product shown to be carcinogenic, mutagenic, and teratogenic. A feasible detoxification pathway for NDMA is a three-step bio-reduction that leads to ammonia and dimethylamine. This study examines the bio-reduction of NDMA in a H2-based membrane biofilm reactor (MBfR) that also is active in nitrate and sulfate reductions. In particular, the study investigates the effects of H2 availability and the relative loadings of NDMA, nitrate, and sulfate, which potentially are competing electron acceptors. The results demonstrate that NDMA was bio-reduced to a major extent (i.e., at least 96%) in a H2-based MBfR in which the electron-equivalent fluxes from H2 oxidation were dominated by nitrate and sulfate reductions. NDMA reduction kinetics responded to NDMA concentration, H2 pressure, and the presence of competing acceptors. The most important factor controlling NDMA-reduction kinetics was the H2 availability, controlled primarily by the H2 pressure, and secondarily by competition from nitrate reduction.     

Assessment of the functionality of a pilot-scale reactor and its potential for electrochemical degradation of calmagite, a sulfonated azo-dye

Electrochemical degradation (ECD) is a promising technology for in situ remediation of diversely contaminated environmental matrices by application of a low level electric potential gradient. This investigation, prompted by successful bench-scale ECD of trichloroethylene, involved development, parametric characterization and evaluation of a pilot-scale electrochemical reactor for degradation of calmagite, a sulfonated azo-dye used as a model contaminant. The reactor has two chambers filled with granulated graphite for electrodes. The system has electrical potential, current, conductivity, pH, temperature, water-level and flow sensors for automated monitoring. The reactor supports outdoor and fail-safe venting, argon purging, temperature regulation and auto-shutdown for safety. Treatment involves recirculating the contaminated solution through the electrode beds at small flow velocities mimicking low fluid-flux in groundwater and submarine sediments. The first phase of the investigation involved testing of the reactor components, its parametric probes and the automated data acquisition system for performance as designed. The results showed hydraulic stability, consistent pH behavior, marginal temperature rise (<5 degrees C) and overall safe and predictable performance under diverse conditions. Near complete removal of calmagite was seen at 3-10V of applied voltage in 8-10h. The effects of voltage and strength of electrolyte on degradation kinetics have been presented. Further, it was observed from the absorption spectra that as calmagite degrades over time, new peaks appear. These peaks were associated with degradation products identified using electrospray ionization mass spectrometry. A reaction mechanism for ECD of calmagite has also been proposed.