污泥静态好氧发酵中堆体板结与通风的研究

为研究污泥静态好氧发酵中板结对强制通风和发酵进程的影响,降低通风能耗,基于理论研究确定了压降为强制通风风量的决定性因素,并通过实验获取不同发酵阶段和强制通风条件下的堆体通风量和抗剪强度数据,分析堆体内板结的形成规律,通过计算验证板结的形成和消失对通风的影响,提出了需要改善通风的时间节点;然后基于风机的变频控制研究了风机功率变化对强制通风的影响。提出的通风解决方案采用阶段变频通风,实现了堆体温度和通风风量的有效控制。     

污泥膜覆盖好氧发酵堆体流场模拟及应用研究

运用Gambit软件建立了污泥好氧发酵堆体的多孔介质模型,通过自行设计的实验装置获得了堆体的通风粘性阻力系数和惯性阻力系数以及功能膜压差与透气量之间的关系,用Fluent软件分析了堆体不同截面形状及底部通风管数量对堆体通风均匀性的影响,为确定合理的通风管数量及截面几何形状提供理论依据。对上海奉贤区城镇污水厂污泥处理工程发酵仓进行堆体流场模拟,确定堆体采用小拱形截面形状,堆高2 m,宽8 m,底部设置4条通风管,实际运行效果良好。     

污泥膜覆盖好氧发酵堆乍流场模拟及应用研究

运用Gambit软件建立了污泥好氧发酵堆体的多孔介质模型，通过自行设计的实验装置获得了堆体的通风粘性阻力系数和惯性阻力系数以及功能膜压差与透气量之间的关系，用Fluent软件分析了堆体不同截面形状及底部通风管数量对堆体通风均匀性的影响，为确定合理的通风管数量及截面几何形状提供理论依据。对上海奉贤区城镇污水厂污泥处理工程发酵仓进行堆体流场模拟，确定堆体采用小拱形截面形状，堆高2m，宽8m，底部设置4条通风管，实际运行效果良好。     

污泥膜覆盖好氧发酵堆体流场模拟及应用研究简

运用Gambit软件建立了污泥好氧发酵堆体的多孔介质模型，通过自行设计的实验装置获得了堆体的通风粘性阻力系数和惯性阻力系数以及功能膜压差与透气量之间的关系，用Fluent软件分析了堆体不同截面形状及底部通风管数量对堆体通风均匀性的影响，为确定合理的通风管数量及截面几何形状提供理论依据。对上海奉贤区城镇污水厂污泥处理工程发酵仓进行堆体流场模拟，确定堆体采用小拱形截面形状，堆高2 m，宽8 m，底部设置4条通风管，实际运行效果良好。     

污水污泥发酵制园林营养土的好氧-厌氧交替方式控制研究

为使污水污泥发酵后制成的园林营养土符合无害化、营养化、腐殖化的要求,通过好氧-厌氧交替试验,考察了不同通风方式、好氧-厌氧交替方式下的大肠菌群数量、发酵温度、有效氮、有效磷、腐殖质等的变化,以确定交替试验的最佳条件.结果表明,污水污泥发酵制园林营养土较佳的通风方式为:通气量1.4～2.8 m3/(h·t)、通气5 mi...     

卧式螺旋污泥好氧动态堆肥技术的研究

利用卧式螺旋式污泥好氧堆肥装置进行间歇式动态堆肥,对污水厂厌氧消化污泥进行了中温堆肥试验研究.通过控制各组堆肥的含水率、物料配比和通气量,重点探讨各种条件下堆体温度与有机物降解的关系.试验结果表明,厌氧消化污泥以木屑为调理剂在装置中可以实现好氧堆肥处理,其适宜的物料控制参数为:污泥:木屑=10:1～1.5(湿重比),堆肥含水率50%～60%;过程控制参数为:通风量为6.7～8.3 m3/h·t,发酵周期为8 d,温度45℃.     

好氧颗粒污泥对膜生物反应器污泥性能的影响

采用膜生物反应器进行含酚废水的处理,探讨投加好氧颗粒污泥对反应器中污泥性能的影响。结果表明,在膜生物反应器中投加好氧颗粒污泥能有效改善污泥性能,提高处理效果。从采用絮状污泥到逐渐增加好氧颗粒污泥投加量为100%的过程中,反应器中污泥浓度明显提高,MLSS由5 582 mg/L增加到8 168 mg/L;沉降性能得到改善,SVI由135.85 mL/g下降到29.36 mL/g;疏水性增强,Zeta电位由-20.302 mV升高到-4.325 mV;对含酚废水中COD、NH3-N的降解能力明显提高,COD、NH3-N、NO3-N去除率分别由87.3%、83.2%、55.3%增加到99.2%、94.9%、66.3%。改善了膜污染现象,膜通量衰减率由63.3%降低到42.8%。用二元多项式三维回归分析,得到污染物去除率关于好氧颗粒污泥投加量和反应器运行时间的二元方程,对指导好氧颗粒污泥膜生物反应器的连续运行具有重要意义。     

好氧颗粒污泥用于膜污染的控制

膜生物反应器在运行过程中容易引起严重的膜污染,从而限制了膜生物反应器在实际废水处理工程中的应用.从污泥特性角度分析了好氧颗粒污泥的特点和减缓膜污染的原因,并且与活性污泥比较,提出好氧颗粒污泥减缓膜污染的优势,为膜污染的控制提出了新的思路和方法.     

城市污水污泥发酵制园林营养土中微生物的变化分析

通过桶装发酵装置,进行城市污水污泥发酵制园林营养土过程中微生物的变化研究,测试不同好氧-厌氧交替组的发酵温度以及细菌、真菌、放线菌数量等的变化,探讨发酵温度与微生物变化的规律.结果表明,夏季不同发酵方式的发酵温度在50℃以上的持续时间均长于冬季,且夏季好氧-厌氧交替发酵的发酵温度在55℃以上的持续时间长于好氧发酵;冬季与夏季的好氧、好氧-厌氧交替发酵后,堆料中的粪大肠菌群数量均达到了《城镇污水处理厂污泥处置园林绿化用泥质》(CJ 248-2007)的卫生学指标要求;夏季好氧-厌氧交替发酵过程中,厌氧后发酵温度有所下降,好氧后发酵温度又有所回升;无论好氧还是好氧～厌氧交替发酵中,细菌均为优势种群,真菌、放线菌数量比细菌数量低2～6个数量级.     

好氧颗粒污泥动态膜生物反应器工艺参数及运行性能

以一体式尼龙筛网动态膜生物反应器(DMBR)为研究体系,与好氧颗粒污泥相结合,形成新的好氧颗粒污泥动态膜生物反应器(AGDMBR),探讨了在新工艺条件下对COD、氨氮的去除,以及出水浊度的变化,与活性污泥动态膜生物反应器(DMBR)做比较,研究了进水流量、曝气量等工艺运行参数与膜污染之间的关系,并对系统中污泥的EPS进行分析。结论表明,AGDMBR系统对COD和NH4+-N的平均去除率分别为91%和95%,出水浊度为6 NTU,处理效果均优于DMBR系统;AGDMBR系统在运行过程中膜污染速度随进水流量的增大而加快;曝气量为125～150 L/h时,膜通量持续时间最长;AGDMBR系统比DMBR系统在膜污染的延缓上具有明显的优势。     

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.     

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.     

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.     

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.     

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.     

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.