污水生物生态处理工艺中的脱氮机理研究

通过水解池-美人蕉湿地、水解/接触氧化池-菖蒲湿地现场实验装置考察了生物-生态工艺深度净化分散生活污水的效果。结果表明,水解池-美人蕉湿地尽管湿地停留时间达到7 d,出水NH⁺₄-N仍难以达到一级A（GB18918-2002）标准;而增加接触氧化池后,湿地停留时间仅2 d,组合工艺出水水质远优于一级A出水要求。美人蕉湿地脱氮的主要途径是湿地微生物的硝化/反硝化,植物吸收约占28%。对经接触氧化处理,NH⁺₄-N、NO^-₃-N浓度均较高的进水,菖蒲湿地可在C/N小于2时高效脱氮。菖蒲湿地对TN的去除占组合工艺TN去除量的79%,其中植物吸收仅占湿地除氮总量的8%。湿地介质的厌氧氨氧化活性试验表明,菖蒲湿地介质表面的微生物在无有机碳源存在的条件下,可使培养液中的NH⁺₄-N与NO^-₃-N、NO^-₂-N短期内发生同步脱氮,厌氧氨氧化可能是菖蒲湿地在进水低碳源条件下脱氮的主要原因。     

花叶芦竹水平潜流人工湿地脱氮性能研究

采用花叶芦竹水平潜流人工湿地处理生活污水,对其脱氮性能进行研究。结果表明：在HRT＝5 d,对TOC,NH⁺₄-N,NO^-₂-N,NO^-₃-N和TN的去除效果分别达到92％、93％、84％、51％和88％,相应空白湿地的去除率分别为91％、85％、-232％、-203％和66％。大部分TOC在湿地的前端被去除。花叶芦竹可以直接吸收氮素,向湿地输送氧气,通过根系分泌物提供碳源。因此,花叶芦竹人工湿地具有很好的硝化反硝化能力,实现了良好的脱氮性能。     

低温条件下BAF+SPD组合工艺对滇池入湖河水的脱氮效果

为缓解湖泊富营养化问题,需进一步降低入湖河流氮的含量。针对滇池流域新运粮河的低C/N水质特征,研究了冬季低温条件下的微曝气生物滤池（BAF）及固相反硝化（SPD）组合异位脱氮工艺。结果表明,BAF+SPD组合工艺启动挂膜阶段,约3周后,NH₄⁺-N的去除率达80%以上,而反硝化细菌增殖相对缓慢,约5周后,NO₃^--N的去除率达80%以上;稳定运行的低温阶段,除降雨时间外,NH₄⁺-N平均去除率达80%,出水NH₄⁺-N浓度<1 mg/L;NO₃^--N平均去除率达到85%以上,出水NO₃^--N浓度<1 mg/L;TN平均去除率达80%以上,出水TN浓度<2 mg/L,主要水质指标达到国家地表水Ⅴ类标准。     

一体化A/O移动床生物膜反应器中DO、TN分布及脱氮效果研究

采用一体化A/O移动床生物膜法工艺,以模拟生活污水研究了该工艺的除碳脱氮效果,并对一体化移动床生物膜反应器的好氧区和缺氧区各纵向断面的COD、DO、NH₃-N、TN、NO^-₃-N和NO^-₂-N进行了检测,通过对缺氧区各断面的DO和TN浓度分布情况,分析了脱氮的产生过程。试验结果表明: 在水力停留时间HRT＝12 h,好氧区DO保持5 mg/L左右,COD进水浓度处于250～400 mg/L时,COD的去除率均在90%以上,且出水COD均在40 mg/L以下;TN进水浓度为20～50 mg/L时,NH₃-N去除率高于90%,其出水浓度可达到5 mg/L以下,脱氮效率也较高,TN去除率可达到65%～85%。COD和NH₃-N的浓度分布状况表明该一体化A/O移动床生物膜反应器的流态趋于全混式。     

温度对复合厌氧折流板膜生物反应器处理生活污水效能的影响简

将新型CAMBR反应器（厌氧折流板反应器（ABR）与膜生物反应器（MBR）优化组合）用于处理生活污水,研究温度对该反应器处理效能的影响。实验水力停留时间7.5 h,混合液回流比设置为200%,pH值为6.5~8.5,溶解氧3 mg/L左右。控制3个温度梯度：高温（32~37℃）,中温（20~25℃）,低温（5~10℃）,每个温度运行35 d。结果表明,在高温条件下,系统出水COD、NH₄⁺-N、TN和TP平均浓度分别为25、0.5、12.5和0.7 mg/L。在中温条件下,系统出水COD、NH₄⁺-N、TN和TP浓度分别30、1.2、12.5和0.4 mg/L。在低温条件下,COD和TP分别经过15 d和20 d调整适应,出水可恢复至35 mg/L和1 mg/L。由于低温（10℃以下）对硝化细菌产生强烈抑制,出水NH₄⁺-N去除率最终稳定在35%,TN去除率为40%。低温条件下,该反应器应用于污水处理中需注意适当保温,以保证出水水质。     

复合沸石滤床修复北方景观水体的实验研究

以天然矿物质沸石、细砂及煤渣取代传统滤料构建复合基质生态床,表面种植景观植物,采用下向流-上向流运行方式修复北方景观水体。分别进行静态实验及不同循环速率下的动态实验,考察对水体污染物去除过程。结果表明,2种运行方式下对水体NH⁺₄-N去除率都在85%以上,其中以1 h为循环周期的运行方式去除率达97%,较静态提高12.8%;TN去除率最高为84%;TP去除不稳定,过程缓慢。煤渣层对NH⁺₄-N的去除效果差,硝化作用不彻底与反硝化作用的加强使下层出水NH⁺₄-N 、NO^-₂-N及NO^-₃-N浓度均高于上层。提高循环速率有利于对氮的去除。     

UASB反应器厌氧氨氧化菌的脱氮特性研究

研究UASB厌氧氨氧化（ANAMMOX）反应器运行情况,采用普通城市污水厂活性污泥接种,人工合成废水,pH值在7.4～7.8之间,温度控制在(32±1)℃。在反应器稳定运行270～450 d之间的180 d中,对NH⁺₄-N和NO^-₂-N去除率均达到99.9％以上,总氮去除率保持在90％以上,NO^-₃-N产生量在20～30 mg/L之间波动。研究表明,UASB厌氧氨氧化反应器处理废水效果明显,对NH⁺₄-N、NO^-₂-N和TN去除率高,NO^-₂-N和NH⁺₄-N比值可以指示厌氧氨氧化反应器性能的演变。UASB反应器稳定运行阶段容积负荷的影响较小,ANAMMOX菌对合成废水适应性强,反应器抗冲击能力较强,受冲击后恢复迅速。出水pH值稳定在8.5附近,pH值变化情况可作为反应器运行状况的指示。关键词硝化厌氧氨氧化上流式厌氧污泥床生物脱氮     

利用城市生态河道深度净化污水处理厂出水的工程技术研究

提出了城市生态河道工程构建的技术方法,并研究了示范工程对城市污水处理厂出水的深度净化规律。实验结果表明,在保证生态景观功能的前提下,将生态河道技术工艺用于污水处理厂出水的深度净化,能够高效、稳定地去除氮磷等营养物,河道出水可以满足城市景观水体补充水源的水质要求,出水TP、PO^3-₄、TN、NH₃-N和NO₃-N平均值分别达到0.263、0.116、2.570、0.752和2.438 mg/L,去除率分别达到85.4%、92.8%、60.8%、39.7%和77.2%。     

SBR-BAF工艺处理效能的试验研究

根据生物除磷和脱氮的机理,污水的脱氮除磷存在基质竞争和泥龄等方面的矛盾。为了分析和解决这个问题,设计开发了一种新的污水生物处理工艺——SBR-BAF复合工艺,并以模拟城市生活污水为处理对象对该工艺的处理效能进行了考察。试验结果表明,系统对COD（不计BAF加入的外碳源）、TP、NH⁺₄-N和TN的平均去除率分别为96%、98%、93%和84%,出水中COD、TP、NH⁺₄-N和TN的平均浓度分别为20、0.23、3.24和7.68 mg/L,各项水质指标均达到《城镇污水处理厂污染物排放标准》（GB 18918-2002 ) 规定的一级标准中的A标准。     

不同填充率对移动床生物膜反应器的产泥性能影响研究

研究了不同填充率下（10%～70%）移动床生物膜反应器的生物膜特征和处理效果,以及填充率与污泥产率的关系。结果表明：随着填充率的增加,填料上生物膜厚度逐渐减少,反应器中附着微生物浓度逐渐增加;污泥产率因填充率不同而有很大差异,同一个反应器内污泥产率随填充率的增加而减少;在进水COD为400 mg/L、NH⁺₄-N为40 mg/L、水力停留时间为12 h条件下,不同填充率下COD去除率均可达到94%以上,NH⁺₄-N去除率达到97%以上。     

Chloroaromatic pollutants in mussels incubated in two finnish watercourses polluted by industry

Concentrations of different chlorinated compounds were measured in mussels incubated in two polluted watercourses, a river (the River Kymijoki) and a lake (Lake Vanaja) for four weeks in summer 1995. The sum concentrations of polychlorinated phenols (PCP) and biphenyls (PCB) were both about 1 μg/g lipid weight (lw) in Lake Vanaja mussels, while in the River Kymijoki mussels PCPs were non-detectable and PCBs were measured 120 ng/g lIw. The concentrations of toxic polychlorinated dibenzo-p-dioxin (PCDD) and dibenzofuran (PCDF) congeners ranged between <17 and 370 pg/g Iw in Lake Vanaja mussels and between <38 and 11,000 pg/g lw in the River Kymijoki mussels. Polychlorinated diphenyl ethers (PCDE) were detected in the mussels incubated in the River Kymijoki (0.4–1.1 ng/g Iw), but not in those incubated in Lake Vanaja. Polychlorinated phenoxyanisoles (PCPA) were measured 33 ng/g lw and polychlorinated phenoxyphenols (PCPP) 300 ng/g lw in the mussels incubated in the River Kymijoki. PCPAs were also detected in reference samples, which were sediment and pike from the River Kymijoki and Baltic salmon, seal and white-tailed sea eagle.     

Evaluation of trichloroethene recovery processes in heterogeneous aquifer cells flushed with biodegradable surfactants

The ability of two biodegradable surfactants, polyoxyethylene (20) sorbitan monooleate (Tween 80) and sodium dihexyl sulfosuccinate (Aerosol MA), to recover a representative dense non-aqueous-phase liquid (DNAPL), trichloroethene (TCE), from heterogeneous porous media was evaluated through a combination of batch and aquifer cell experiments. An aqueous solution containing 3.3% Aerosol MA, 8% 2-propanol and 6 g/l CaCl(2) yielded a weight solubilization ratio (WSR) of 1.21 g TCE/g surfactant, with a corresponding liquid-liquid interfacial tension (IFT) of 0.19 dyn/cm. Flushing of aquifer cells containing a TCE-DNAPL source zone with approximately two pore volumes of the AMA formulation resulted in substantial (>30%) mobilization of TCE-DNAPL. However, a TCE mass recovery of 81% was achieved when the aqueous-phase flow rate was sufficient to displace the mobile TCE-DNAPL toward the effluent well. Aqueous solutions of Tween 80 exhibited a greater capacity to solubilize TCE (WSR=1.74 g TCE/g surfactant) and exerted markedly less reduction in IFT (10.4 dyn/cm). These data contradict an accepted empirical correlation used to estimate IFT values from solubilization capacity, and indicate a unique capacity of T80 to form concentrated TCE emulsions. Flushing of aquifer cells with less than 2.5 pore volumes of a 4% T80 solution achieved TCE mass recoveries ranging from 66 to 85%, with only slight TCE-DNAPL mobilization (<5%) occurring when the total trapping number exceeded 2 x 10(-5). These findings demonstrate the ability of Tween 80 and Aerosol MA solutions to efficiently recover TCE from a heterogeneous DNAPL source zone, and the utility of the total trapping number as a design parameter for a priori prediction of DNAPL mobilization and bank angle formation when flushing with low-IFT solutions. Given their potential to stimulate microbial reductive dechlorination at low concentrations, these surfactants are well-suited for remedial action plans that couple aggressive mass removal followed by enhanced bioremediation to treat chlorinated solvent source zones.     

Book review

The Pesticide Manual ‐ A World Compendium, 8th Edition, C.R. Worthing, Editor and S.B. Walker, Assistant Editor, British Crop Protection Council, BCPC Publications Sales, Bear Farm, Binfield, Bracknell, Berkshire RG12 5QE, England. 1987, 1100 pp., UK £50; Overseas £56. ISBN 0–948404–01–9.     

The variation of street air levels of PAH and other mutagenic PAC in relation to regulations of traffic emissions and the impact of atmospheric processes

The occurrence of particle associated PAH and other mutagenic PAC was determined in 1996 in the street air of Copenhagen. In addition, particle extracts were tested for mutagenicity. The measurements were compared with previous measurements in 1992/1993. The levels had decreased in this period. The decrease was caused by an implementation of light diesel fuels for buses and the exchange of older petrol-driven passenger cars with catalystequipped new ones. About 65% of the reduction was caused by the application of the light diesel fuels. Under special conditions, chemical processes in the atmosphere produced many more mutagens than the direct emissions. The concentrations of S-PAC and N-PAC were 10 times lower than those of PAH, while the levels of oxy-PAH were in the same order of magnitude as those of PAH. Benzanthrone, an oxy-PAH, is proposed to be formed in the atmosphere in addition to direct emissions. Benzo(a)pyrene, often applied as an air quality criteria indicator, was photochemically degraded in the atmosphere. A strong increase in the mutagenic activities was observed to coincide with a depletion of benzo(a)pyrene.     

Organochlorine compounds in a three-step terrestrial food chain

The concentrations of 15 organochlorine chemicals (PCBs and pesticides) were studied in a Central European oak wood food chain system: Great tit (Parus major), caterpillars (Tortrix viridana, Operophtera brumata, Erannis defoliaria), and oak-leaves (Quercus robur). Juvenile tits receive organochlorines from the mother via egg transfer and, eventually to a greater extent, from the caterpillar food source during nestling period. The concentrations of PCB 153 (2,2′,4,4′,5,5′-hexachlorobiphenyl, the most abundant in this study) was found in leaf material at ca. 1 ng/g, in caterpillars 10 ng/g, and in bird eggs 170 ng/g on an average and on a dry mass basis.     

The chemical stability of formulations of some hydrolyzable insecticides in aqueous mixtures with hydrolysis catalysts

Abstract

The active ingredients in commercial formulations of malathion, oxamyl, carbaryl, diazinon, and chlorpyrifos diluted to “spray tank”; concentrations with buffered distilled or natural water of pH 4–9 were stable for at least 24 hr. Formulations of trichlorfon were not stable at pH 7 or above but disappearance rates were slower than for the pure chemical in homogeneous solution. Cupric ion was observed to be an effective catalyst for the hydrolysis of a variety of pure organophosphorus insecticides but did not catalyze hydrolysis of the active ingredients of the formulations examined. Increasing the dilution of the formulation increased the susceptibility of malathion, oxamyl, and carbaryl to hydrolysis.     

Observations on the influence of water and soil pH on the persistence of insecticides

Abstract

The pH‐disappearance rate profiles were determined at ca. 25°C for 24 insecticides at 4 or 5 pH values over the range 4.5 to 8.0 in sterile phosphate buffers prepared in water‐ethanol (99: 1 v/v). Half‐lives measured at pH 8 were generally smaller than at lower pH values. Changes in half lives between pH 8.0 and 4.5 were largest (>1000x) for the aryl carbamates, carbofuran and carbaryl, the oxime carbamate, oxamyl, and the organophosphorus insecticide, trichlorfon. In contrast, half lives of phorate, terbufos, heptachlor, fensulfothion and aldicarb were affected only slightly by pH changes. Under the experimental conditions described half lives at pH8 varied from 1–2 days for trichlorfon and oxamyl to >1 year for fensulfothion and cyper‐methrin. Insecticide persistence on alumina (acid, neutral and basic), mineral soils amended with aluminum sulfate or calcium hydroxide to different pH values and four natural soils of different pH was examined. No correlation was observed between the measured pH of these solids and the rate of disappearance of selected insecticides applied to them. These observations demonstrate the difficulty of extrapolating the pH dependent disappearance behaviour observed in homogeneous solution to partially solid heterogeneous systems such as soil.     

Teratological effects of pesticides in vertebrates: a review

Abstract

In the last decades, the use and misuse of pesticides in the agriculture have increased, having a severe impact on ecosystems and their fauna. Although the various effects of pesticides on biodiversity have been already documented in several studies, to our knowledge no consistent overview of the impact of pesticides in vertebrates, both terrestrial and aquatic, is available. In this review, we try to present a concise compilation of the teratogenic effects of pesticides on the different classes of vertebrates – mammals, birds, reptiles, amphibians and fish.     

Radionuclides in pinon pine (Pinus edulis) nuts from los alamos national laboratory lands and the dose from consumption

Abstract

One of the dominant tree species growing within and around the eastern portion of Los Alamos National Laboratory (LANL), Los Alamos, NM, lands is the pinon pine (Pinus edulis). Pinon pine is used for firewood, fence posts, and building materials and is a source of nuts for food—the seeds are consumed by a wide variety of animals and are also gathered by people in the area and eaten raw or roasted. This study investigated the (1) concentration of ³H, ¹³⁷Cs, ⁹⁰Sr, ^totU, ²³⁸Pu, ^{239, 240}Pu, and²⁴¹ Am in soils (0‐ to 12‐in. [31 cm] depth underneath the tree), pinon pine shoots (PPS), and pinon pine nuts (PPN) collected from LANL lands and regional background (BG) locations, (2) committed effective dose equivalent (CEDE) from the ingestion of nuts, and (3) soil to PPS to PPN concentration ratios (CRs). Most radionuclides, with the exception of ³H in soils, were not significantly higher (p < 0.10) in soils, PPS, and PPN collected from LANL as compared to BG locations, and concentrations of most radionuclides in PPN from LANL have decreased over time. The maximum net CEDE (the CEDE plus two sigma minus BG) at the most conservative ingestion rate (10 lb [4.5 kg]) was 0.0018 mrem (0.018 μSv); this is far below the International Commission on Radiological Protection (all pathway) permissible dose limit of 100 mrem (1000 μSv). Soil‐to‐nut CRs for most radionuclides were within the range of default values in the literature for common fruits and vegetables.     

Degradation and sorption of imidacloprid in dissimilar surface and subsurface soils

Degradation and sorption/desorption are important processes affecting the leaching of pesticides through soil. This research characterized the degradation and sorption of imidacloprid (1-[(6-chloro-3-pyridinyl)-methyl]-N-nitro-2-imidazolidinimine) in Drummer (silty clay loam) and Exeter (sandy loam) surface soils and their corresponding subsurface soils using sequential extraction methods over 400 days. By the end of the incubation, approximately 55% of imidacloprid applied at a rate of 1.0 mg kg^?1 degraded in the Exeter sandy loam surface and subsurface soils, compared to 40% of applied imidacloprid within 300 days in Drummer surface and subsurface soils. At the 0.1 mg kg^?1 application rate, dissipation was slower for all four soils. Water-extractable imidacloprid in Exeter surface soil decreased from 98% of applied at day 1 to > 70% of the imidacloprid remaining after 400 d, as compared to 55% in the Drummer surface soil at day 1 and 12% at day 400. These data suggest that imidacloprid was bioavailable to degrading soil microorganisms and sorption/desorption was not the limiting factor for biodegradation. In subsurface soils > 40% of ¹⁴C-benzoic acid was mineralized over 21 days, demonstrating an active microbial community. In contrast, cumulative ¹⁴CO₂ was less than 1.5% of applied ¹⁴C-imidacloprid in all soils over 400 d. Qualitative differences in the microbial communities appear to limit the degradation of imidacloprid in the subsurface soils.