碳源对静置/好氧/缺氧SBR脱氮除磷性能的影响

以合成废水为研究对象,分别以丙酸钠、乙酸钠/丙酸钠(1∶2碳/碳)、乙酸钠和葡萄糖为外加碳源,建立同步脱氮除磷的静置/好氧/缺氧序批式反应器(SOA-SBR)。通过比较长期运行过程中各反应器的脱氮除磷效果,考察不同碳源对静置/好氧/缺氧SBR脱氮除磷性能的影响,并通过分析典型周期内氮、磷元素及微生物体内储能物质的变化,探究其影响机理。结果表明,丙酸钠为碳源时SBR能获得96%的最佳除磷效果以及78.3%的总氮去除率;乙酸钠为单一碳源时可取得92.3%的除磷率和93.7%的总氮去除率;而混合碳源对于氮、磷的去除能力介于丙酸钠和乙酸钠之间;葡萄糖为单一碳源时系统对于磷和总氮的去除率仅26%和36.7%。丙酸钠和乙酸钠均能取得良好的同步脱氮除磷效果,但乙酸钠对总氮去除能力更佳。通过分析典型周期中内聚物含量变化表明,微生物体内聚羟基脂肪酸酯(PHA)和糖原质含量的变化与系统反硝化能力和溶解性正磷酸盐(SOP)去除效果呈正相关性。     

不同碳源和泥龄对反硝化聚磷的影响

在4个SBR装置(1#~4#)中,对4种不同比例的丙酸/乙酸合成废水采用厌氧/缺氧方式驯化富集反硝化聚磷菌(DPB),研究了碳源浓度和污泥龄对除磷的影响。实验结果表明:(1)厌氧段碳源COD浓度越高,释磷越充分,溶解性正磷酸盐(SOP)去除率越高;但当碳源COD浓度超过某个浓度值时,未反应完全的有机物残留于后续缺氧段对缺氧吸磷产生抑制作用。(2)污泥龄SRT=15 d时,活性污泥的性能较好,达到了较好的除磷效果。(3)在相同碳源浓度和相同的污泥龄下,随着丙酸/乙酸比例的提高,SOP的去除率逐渐的降低。说明在厌氧/缺氧环境下,碳源中丙酸比例的提高不利于系统中磷的去除。高乙酸含量的碳源更适合反硝化除磷系统。     

不同碳源添加量对垂直流人工湿地污水处理效果的影响

以垂直流人工湿地小试系统为研究对象,采用碱处理过的千屈菜(Lythrum salicaria)作为反硝化碳源补充材料,探讨了不同碳源添加量对系统COD及氮、磷去除效果的影响。结果表明,一定剂量经过碱处理的千屈菜材料可以为人工湿地系统脱氮提供反硝化所需要的碳源,而且具有缓效持续释放的特点。添加此碳源材料可明显提高系统的脱氮效率,最高可提升30.85%,但随着C/N比的增加,硝态氮去除率逐渐降低,C/N比为3、5、8时分别为91.20%、87.72%和84.19%。添加碳源量达到C/N比为3时系统能够发生最大程度反硝化,此时不仅人工湿地系统脱氮效果得到提高,同时人工湿地除磷能力也有所增强。碱处理过的千屈菜材料在本系统中的最适宜添加量为5 g,即100 g/m2(C/N=3),远低于在进水中为满足反硝化所需调控的C/N比(5～8),可以节约外加碳源成本。     

高氨氮污泥脱水液短程硝化反硝化的启动及稳定

采用A/O-CSTR工艺处理高氨氮污泥脱水液。进水氨氮浓度浓度约为375 mg/L,C/N比小于1.0,反硝化碳源明显不足。A/O反应器完成短程硝化反应,CSTR定期投加初沉污泥作为碳源进行反硝化。两者联合达到总氮去除的目的。实验研究短程硝化反应的启动过程,以及CSTR出水回流对短程硝化和系统脱氮效果的影响。实验结果表明系统具有良好的硝化反硝化效果。A/O反应器亚硝酸盐积累率迅速提高并稳定在90%以上。CSTR有效利用初沉污泥实现了稳定的反硝化。出水回流有利于提高总氮去除率,在回流比为200%时,系统平均总氮去除率达到85%以上。     

A2/O工艺中的反硝化除磷

A2/O工艺是一种最简单的同步脱氮除磷工艺,但由于其系统中固有的基质竞争和污泥龄等矛盾,在实际应用中特别是处理低C/N比污水时脱氮除磷效率较低.反硝化除磷工艺作为近年来颇受关注的污水生物处理新技术.由于在脱氮除磷过程中可以在碳源利用上耦合,可从一定程度上缓解A2/O工艺中的基质竞争矛盾,使得其在处理低C/N比污水时也能实现较高的脱氮除磷效率.就反硝化除磷的技术原理,结合其在A2/O工艺中的最新研究成果及其控制策略,对A2/O工艺中的反硝化除磷的实现、维持及影响因素进行了分析和探讨,并对其发展方向进行了展望.     

某污水处理厂A2/O工艺冬季生物反硝化过程的影响因素研究

针对污水处理厂冬季反硝化脱氮效率不佳的问题,以常州市某污水处理厂A~2/O工艺为研究对象,模拟探讨了不同外加碳源、碳源投加量、溶解氧(DO)和硝态氮浓度对生物处理系统反硝化脱氮能力的影响。结果表明,外加有机碳源对系统的反硝化效能有明显的强化效果。3种外加有机碳源(乙酸、乙醇和乙酸钠)中,乙酸为最佳碳源。当乙酸投加量为40mg/L时,系统反硝化脱氮效率最高,比反硝化速率可达1.964mg/(g·h),反硝化碳耗最少,为7.14 mg/mg。DO与比反硝化速率成反比,DO≤0.20mg/L时,反硝化能力最强。硝态氮初始质量浓度为20mg/L左右时,反硝化能力最强。在实际工程应用中,可以通过提高硝化效果或直接调整回流比实现反硝化脱氮最优条件,将有助于提高系统的冬季脱氮效果。     

C/N对单级脱氮系统N_2O排放量及其途径的影响

采用4组0.5 L的批式反应器,调节进水初始NH_4~+-N为100 mg·L~(-1),控制温度为30℃,DO为(2.00±0.20)mg·L~(-1),以葡萄糖为有机碳源,采用化学抑制法研究进水C/N分别为0、0.5、1.0和1.5时,单级脱氮系统的氮转化情况、N_2O排放量及N_2O排放途径。结果表明,反应器进水C/N从0升高至1.5,在6 h时系统TN去除率由14.5%增至23.5%,而系统N_2O排放量由180μg减至10μg,N_2O转化率由2.5%降至0.1%。随着进水C/N的升高,氨氧化菌(AOB)反硝化产生的N_2O排放量在3.6~11.7μg之间波动,而同步硝化-反硝化产生的N_2O排放量降幅明显,由176.8μg降至5.3μg。当C/N为较低的0和0.5时,同步硝化-反硝化对N_2O排放贡献率均达到85%以上,系统N_2O排放途径主要为同步硝化-反硝化;当C/N为较高的1.0和1.5时,AOB反硝化对N_2O排放贡献率为45.9%和26.5%,系统N_2O排放途径主要为同步硝化-反硝化和AOB反硝化作用。     

进水碳氮比对SUFR系统脱氮除磷影响的特性分析

考察了进水碳氮比（C/N）对螺旋升流式反应器（spiral up-flow reactor,SUFR）系统生物脱氮除磷的影响,试验设计了进水C/N在7～13范围的数种工况,研究了SUFR系统中COD、总磷和氮的变化规律。结果表明,进水C/N对SUFR系统去除COD与TP效果的影响不明显,平均去除率分别为95.2%和93.9%;当进水C/N<9.4时,TN的去除率随C/N的增大而快速提高,而当进水C/N>9.4时,TN的去除率稳定在81.1%～85.6%;SUFR系统的硝化效果较稳定,氨氮的去除率保持在90.5%～98.8%;系统的反硝化作用随C/N的增大有所增强,出水硝酸盐氮浓度逐渐降低。     

双泥膜法SBR脱氮除磷效果研究

通过实验室小试,以人工模拟生活污水为研究对象,考察了基于反硝化除磷理论开发的双泥膜法SBR工艺的脱氮除磷效果。长期试验结果表明：双泥膜法SBR工艺能使硝化菌和除磷菌各自在最佳的环境中生长,解决了传统工艺中脱氮和除磷的矛盾,节省了碳源和能源,并取得了稳定高效的脱氮除磷效果。在进水C∶N∶P为25∶5∶1,换液比为75%的情况下,系统对COD,TP和NH⁺₄-N的平均去除率分别为89.13%、96.12%和86.78%。     

以养殖固体废弃物发酵产物为碳源的SND系统的脱氮除磷效果

在连续低曝气的SBR装置中,采用人工模拟养殖废水培养成熟脱氮除磷污泥,研究了养殖固体废弃物发酵产物为碳源的养殖废水脱氮除磷效果。结果表明:在水力停留时间(HRT)为12 h,溶氧在0.04~1.5 mg/L之间,污泥经过25d的驯化培养,反应器中形成了具有较高活性的同步硝化反硝化能力的污泥,以养殖固体废弃物发酵产物为碳源处理养殖废水,反应器中的COD、NO-3-N和NH+4-N最大去除率分别能达到97.87%、94.95%和88.90%,且NO-2-N完全不发生累积,其中C/N=7.35,即50 g湿重的养殖固体废弃物与2 L的养殖废水配比最佳,脱氮除磷效果最好,对TN的去除率在87%左右,能够较好完成同步脱氮除磷实现养殖固体废弃物的资源化利用,为循环水养殖系统零排放提供技术参考。     

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.