连续流改进A~2/O反应器去污效果及分相培养研究

以生活污水为原水,在常温(25~33℃)条件下采用连续流改进A2/O反应器进行脱氮除磷实验研究。系统内COD降解,TN与TP去除主要在活性污泥段完成,而NH4+-N去除基本在生物接触氧化区完成。从中沉池出水硝态氮影响因素分析可知,选用较高的有机负荷有利于实现系统内分相培养。泥龄对实现系统内微生物异养菌和自养菌的分相培养具有关键影响。当泥龄10 d,可实现系统内异养菌与自养菌的分相培养。     

连续流改进A2/O反应器去污效果及分相培养研究

以生活污水为原水,在常温（25-33℃）条件下采用连续流改进A2/O反应器进行脱氮除磷实验研究。系统内COD降解,TN与TP去除主要在活性污泥段完成,而NH4＋-N去除基本在生物接触氧化区完成。从中沉池出水硝态氮影响因素分析可知,选用较高的有机负荷有利于实现系统内分相培养。泥龄对实现系统内微生物异养菌和自养菌的分相培养具有关键影响。当泥龄〈10 d,可实现系统内异养菌与自养菌的分相培养。     

智能化曝气控制A/O工艺处理低C/N生活污水有效性及其脱氮机制

将新型智能化曝气控制系统(automatic oxygen supply device,AOSD)应用于A/O工艺中,研究AOSD系统曝气模式控制下的A/O工艺(I-A/O)与持续曝气模式的A/O工艺(C-A/O)对低C/N生活污水处理能力的有效性,并从系统活性污泥特性的角度探究I-A/O系统反硝化菌在脱氮过程中对碳素的摄取、利用途径。结果表明:低进水碳源负荷下,I-A/O与C-A/O系统对COD、NH_4~+-N的平均去除率稳定且均达80%以上;I-A/O系统对TN去除率高出C-A/O系统25.97%,其对TN具有明显的去除优势;2套系统对TP均无去除效果。I-A/O系统活性污泥好氧异养菌产率系数Y_H为0.142 mg·mg~(-1),活性污泥衰减系数K_d为0.018 d~(-1),均低于C-A/O系统;在进水低C/N水平下,I-A/O系统活性污泥可通过更强的吸附贮存碳源能力、较低的好氧异养菌竞争压力、溶胞作用为反硝化菌提供更多的碳源以便脱氮反应。C/N是I-A/O系统曝气总量节省率重要影响因素之一,相比于C-A/O系统,其处理低C/N生活污水可节约曝气系统约52%的曝气量。     

生物吸附-多级A/O-活性焦组合工艺对污水中氮磷及有机污染物的去除

利用生物吸附(biological absorption,AB)-多级缺氧/好氧(anaerobic/oxic,A/O)-活性焦滤池组合工艺对城市污水进行处理研究。结果表明:该组合工艺出水COD、TN、TP平均浓度为20、8.5、0.25 mg·L~(-1),对COD、TN、TP平均去除率为95%、76.5%、80%,3个工艺段对有机污染物的平均去除率分别为55%、26%、14%。其中生物吸附段主要去除粒径较大的颗粒态有机物,多级A/O段可以去除进水中53%左右溶解性有机物;活性焦滤池利用活性焦丰富的中孔结构有效吸附多级A/O出水中难生物降解的芳香类及环烷类有机物。该组合工艺能实现高标准出水、高效脱氮除磷、能源节约、资源回收,是具有良好应用前景的污水处理工艺。     

A2/O+硫磺填料柱组合工艺脱氮除磷的效果

以某城市污水厂进水为研究对象,采用A2/O+硫磺填料反应柱组合工艺,考察其对COD、总氮、总磷以及溶解性磷处理效果的改善。组合工艺出水水质稳定后,连续运行55 d,并对工艺的出水进行常规指标分析。结果表明:组合工艺的脱氮除磷效果较单个A2/O工艺都得到了较大的改善,而COD去除效果变化不大。A2/O系统对COD有良好的去除效果,出水的COD平均去除率能达到94%;TN和TP去除效果相对较差,出水平均去除率分别为60%和57.4%。经硫磺填料反应柱的脱氮除磷作用,系统出水TN去除率提高到84%,TP去除率提高到69.8%,COD去除率变化不大,升高到95.3%。     

A~2/O＋硫磺填料柱组合工艺脱氮除磷的效果

以某城市污水厂进水为研究对象,采用A2/O＋硫磺填料反应柱组合工艺,考察其对COD、总氮、总磷以及溶解性磷处理效果的改善。组合工艺出水水质稳定后,连续运行55 d,并对工艺的出水进行常规指标分析。结果表明：组合工艺的脱氮除磷效果较单个A2/O工艺都得到了较大的改善,而COD去除效果变化不大。A2/O系统对COD有良好的去除效果,出水的COD平均去除率能达到94%;TN和TP去除效果相对较差,出水平均去除率分别为60%和57.4%。经硫磺填料反应柱的脱氮除磷作用,系统出水TN去除率提高到84%,TP去除率提高到69.8%,COD去除率变化不大,升高到95.3%。     

活性炭纤维上4-氯酚及焦化废水尾水的O3催化氧化降解实验研究

选择YT-1000型活性炭纤维(ACF)作为催化剂,考察ACF与O3协同作用催化降解水溶液中4-氯酚的最佳反应条件,并将该条件应用于焦化废水生物处理尾水中难降解有机污染物的催化氧化.ACF表面具有丰富的微孔结构,对4-氯酚有良好的吸附作用,在动力学上提高了其与O3反应的起始浓度,并且在ACF表面含氧、含氮等基团的催化作用下发生氧化反应,1 L浓度为100 mg/L的4-氯酚水样中投加2 g ACF反应6 min时,吸附作用对TOC的去除率为43.4%.而ACF协同O3作用时的TOC去除率提高到72.5%,协同增效作用为67.1%;在选定的反应条件下,ACF协同O3降解焦化废水生物处理尾水,60 min时的TOC与色度的去除率分别达到56.8%和96.3%.上述研究过程证明了吸附作用与催化作用的协同能有效降解生物过程不能降解的焦化废水中惰性有机污染物.     

低温下ZCS工艺和改进式ZCS工艺脱氮效率研究及微生物特性分析

考察冬季低温下沸石联合生物吸附再生工艺和改进式沸石联合生物吸附再生工艺对城市污水的脱氮效率,结果表明在HRT为3.5 h下,ZCS工艺出水氨氮为11.65 mg/L,总氮高于20 mg/L.而相同条件下MZCS工艺氨氮出水为5.45 mg/L,总氮去除率比原ZCS工艺提高了11%,均值为16.8 mg/L.通过聚合酶链式技术,变性梯度凝胶电泳和电镜扫描技术发现两工艺微生物多样性、丰度高于传统活性污泥法,兼具活性污泥法和生物膜法的微生物特性.     

高铁酸盐氧化-A/O工艺污泥减量及强化脱氮

为了减少传统生物处理工艺剩余污泥排放量及强化脱氮效果,设计了高铁酸盐氧化-A/O工艺。以模拟生活污水为处理对象,研究对比了破解后不同回流比对高铁酸盐氧化-A/O工艺的污泥减量和强化脱氮效果的影响,并对出水水质和污泥性能进行了综合评价。实验结果表明:剩余污泥破解回流比r为50%时,污泥产率系数YOBS为0.05 g·g~(-1),剩余污泥量减少最多,为46%;高铁酸盐氧化-A/O工艺对TN和NH_4~+-N去除率分别达到71.7%和88.8%,CFS污泥破解液具有较好的可生化性,可被反硝化菌有效利用,脱氮效果明显提高;该运行工况下,污泥浓度、污泥活性均有所提高,污泥沉降性得到改善。此外,污泥破解液引入系统的Fe~(3+)可在一定程度上提高了TP的去除率。高铁酸盐氧化-A/O工艺能够提高污染物去除率,实现污泥减量同步强化脱氮的目的。     

两种A~2/O工艺的活性污泥2D模型动力学参数灵敏度分析

使用GPS-X软件对传统A~2/O工艺和氧化沟型A~2/O工艺的污染物(COD、硝酸盐氮、氨氮和溶解性正磷酸盐)去除效果进行模拟,选用活性污泥2D模型(ASM2D)对厌氧池、缺氧池和好氧池中20个重要动力学参数进行了灵敏度分析。结果发现,在两种A~2/O工艺中,动力学参数对出水COD和硝酸盐氮浓度的灵敏度影响较小,对出水氨氮和溶解性正磷酸盐浓度的灵敏度影响很大。与聚磷菌相关的动力学参数灵敏度最高,与异养菌相关的动力学参数灵敏度最低。参数向上浮动与向下浮动对同一水质指标的影响程度不同,饱和/抑制系数类参数的灵敏度一般低于其他参数。     

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.     

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.     

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.     

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.     

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.     

Patterns of volatile metabolites and nonvolatile trichothecenes produced by isolates of <Emphasis Type="Italic">Stachybotrys,Fusarium, Trichoderma,Trichothecium</Emphasis> and <Emphasis Type="Italic">Memnoniella</Emphasis>

We reported previously that trichodiene, a volatile trichothecene derivative, was produced by a Stachybotrys isolate, also known to produce highly cytotoxic, non-volatile, macrocyclic trichothecenes (satrotoxins). We investigated the relationship between the production of trichodiene and various non-volatile trichothecenes for several molds. Volatile metabolites were concentrated by adsorption on Tenax TA and analyzed by GC/MS, while non-volatile metabolites were separated by HPLC, derivatized and analyzed by GC/MS. Stachybotrys chartarum isolates producing macrocyclic trichothecenes secreted significantly larger amounts of trichodiene and other sesquiterpenes than isolates which only produced simple trichothecenes. The amounts of secreted trichodiene were relatively small in all cases. With the exception of Memnoniella, which excreted small amounts of sesquiterpenes, the other isolates produced varying amounts of sesquiterpenes, including trichodiene, as well as simple tricothecenes, no detectable trichodiene, but large amounts of griseofulvin derivatives. In Stachybotrys there is apparently a correlation between trichodiene and macrocyclic trichothecene production. In the remaining isolates, there was no simple relationship between trichodiene and non-volatile trichothecene synthesis. Trichodiene is produced in larger amounts by Stachybotrys isolates, which also produce satratoxins, but it will be difficult to utilize this metabolite to detect toxic isolates in buildings due to the relatively small amounts excreted.     

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.     

Knowledge transfer initiative between molecular biologists and environmental researchers and regulators

A Natural Environment Research Council (NERC) funded Knowledge Transfer (KT) workshop was held in the United Kingdom (UK) to identify the needs and opportunities in the application of molecular biology and ‘omics’ techniques to environmental monitoring and risk assessment. Attendees highlighted a lack of effective communication between end-users and researchers as well as difficulties with data interpretation as reasons behind the slow uptake of molecular biology and omics techniques. A number of promising areas in which new techniques could be implemented at a practical level in the very near future were identified, thereby raising the profile of these recent technologies and providing vital proof of concept work. Molecular taxonomy, bacterial source tracking and pre-screening of chemicals for potential toxicities were all viewed as areas in which omics and molecular techniques could have immediate value, with the aim of reducing cost, increasing efficiency and providing more comprehensive data of improved quality.     

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.     

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.