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.     

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。     

新型侧向流曝气生物滤池处理生活污水

采用以沸石为填料的新型侧向流曝气生物滤池处理生活污水,考察了水力负荷和气水比的影响.结果表明,LBAF在最佳工况气水比10∶1,A、B段曝气量比1∶1,水力负荷0.43 m3/m2·h下,COD、SS、氨氮、总氮和总磷的去除率分别为88.01%、95.18%、78.97%、52.58%和21.02%;COD去除率随COD容积负荷的增加缓慢下降.氨氮、总氮去除率随COD容积负荷的增大明显下降,氨氮去除率随氨氮容积负荷的增大而明显降低.滤池纳污能力强,不易堵塞,可适当延长反冲周期.     

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。     

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).     

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%。     

两段曝气生物滤池进行生活污水处理及经验模型研究

采用两段曝气生物滤池进行生活污水处理,A段反应器进水负荷分别控制在9.17、15.59、22.01 m3/(m2·d),气水比为6∶1(体积比,下同),而B段气水比则控制在2∶1。试验结果表明,系统出水稳定优质(SCOD<30 mg/L、NH3 N<4 mg/L、SS<10 mg/L),若做进一步的消毒处理后可进行回用。同时,从简化工艺设计的角度出发,针对A段进、出水溶解性COD(SCOD)和反应器高度,建立了一套经验模型。通过大量的试验数据模拟,推算出不同水力负荷下的经验模型常数n和K值,从而为工程设计提供了依据和方法。     

折流曝气生物滤池的特征与处理效能试验研究

折流曝气生物滤池(BBAF)是一种新型生物滤池，为考察其工艺特征和处理效能，对运行时的效果和不同水力条件下的水力混合特性进行了研究。试验表明，BBAF滤池是一种复合流态反应器，单池趋于全混流,而整池趋向平推流；BBAF滤池对COD和SS的去除率稳定在90%以上,对氨氮、总氮和总磷平均去除率分别为88.8%、39.1％和46.5%。     

BAF处理生活污水过程中同步去除H2S的试验研究

采用曝气生物滤池处理生活污水的过程中,以混和臭气的空气为气源,以掺入了陶粒和铁炭颗粒的复合填料为载体,研究了反应器的运行条件和参数,结果表明,以混合臭气的空气作为气源对污水处理过程的需氧量基本无影响.当反应器的进气量为40 L/h,进水容积负荷和进气H2S的浓度分别在0.3～1.6 kg COD/(m3·d)和0.8～2.3 mg/m3之间变化时,可以实现出气和出水中H2S和COD分别小于0.04 mg/m3和90 mg/L,满足同时达标排放的要求.H2S的同步去除可能是通过微生物的氧化分解和形成FeS沉淀来实现的.     

曝气生物滤池处理农村污水的中试研究

采用研制的曝气生物滤池对农村污水进行处理，研究其性能特点和影响因素。结果表明：在气水比为5∶1，水力停留时间（HRT）为15 h，进水COD浓度在250 mg/L以下时，COD和氨氮的去除率分别在80％和90％以上，出水COD和氨氮值达到国家《城镇污水处理厂污染物排放标准》一级A标准；反应器在冬季水温12℃以上运行时出水COD和氨氮值比在夏季运行时有所上升，但去除率仍在80%和90%以上，可以达到排放标准。     

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。     

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。     

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.