垃圾压缩站污水的生物强化处理

垃圾压缩站污水是一种具有高COD、高NH3-N特点的有机污水.以厌氧/好氧组合工艺为基础,通过投加高效菌株对活性污泥系统进行生物强化.实验结果表明,与空白相比,厌氧出水COD去除率提高约30%,好氧出水NH3-N去除率提高约20%.最终出水COD《120 mg/L, NH3-N《25 mg/L,均达到《污水综合排放标准》(GB 8978-1996)二级排放标准.     

交替缺氧/好氧CAST工艺污染物去除特性

以模拟城市污水为处理对象,采用循环式活性污泥法(CAST)反应器,对交替缺氧/好氧模式下系统去除污染物的性能进行了研究。结果表明,运行期间系统内有机物的去除率稳定,出水COD小于40 mg/L,COD平均去除率为91.7%;NH4+-N、TN的平均去除率分别为83.9%、72.4%,出水TN以NO3--N为主;系统的除磷性能良好,磷酸盐的平均去除率为90.6%。此外,出水COD、TN和TP均达到《城镇污水处理厂污染物排放标准》(GB-18918-2002)的一级A要求。     

厌氧折流板反应器处理生活污水的运行特性

以厌氧消化污泥作为厌氧折流板反应器ABR的接种污泥,研究恒温(35℃)条件下ABR处理生活污水的启动和运行特性。实验结果表明,ABR反应器仅用了39 d就完成初次启动,COD去除率一直稳定在60%左右。在以后运行的5个阶段里,即当水力停留时间为4~10 h,容积负荷为1.17~2.9 kg COD/m3.d,反应器对COD的平均去除率基本稳定在70.49%~80.2%;并且当HRT=7 h,VRL=1.612 kg COD/m3.d时,反应器对COD的去除率平均高达80.2%,平均COD出水低于100 mg/L。在实验过程中(除启动阶段外),反应器出水碱度均远远大于进水碱度,VFA均在1.5 mmol/L以下。     

新型厌氧反应器--USSB的启动研究

对上流式分段污泥床反应器在中温(35±2)℃下处理生活污水前的启动过程进行了试验研究.反应器经过40 d的启动后,当进水有机负荷为2.2 kg COD/m3·d时,其COD去除率能稳定在80%左右,出水pH值和碳酸氢盐碱度/VFA分别大于6.5和2,整个系统运行稳定.     

常温下HAR处理低浓度生活污水中试启动

对有效容积为315L的复合式厌氧反应器(hybridanaerobicreactor,HAR)处理低浓度生活污水的启动情况做了研究,结果表明,HAR在常温下是可以启动的,复合式厌氧工艺在启动初期有利于厌氧污泥和有机物的积累。HAR的启动期可分为3个阶段,水温>15℃时,HAR运行34d后,反应器完成启动。水力停留时间(HRT)为6h,COD和SS去除率可达60%以上。容积负荷从0.775kgCOD/m3·d增加到2.227kgCOD/m3·d,去除效率不受影响。下部污泥床层和上部填料层的污泥特性不同,在启动期末,污泥床层有少量颗粒污泥出现。     

上流式缺氧污泥床和好氧生物膜组合脱氮工艺的研究

将上流式颗粒污泥床(USB)用于反硝化和生物膜法用于自养硝化处理蔗糖配水和小区生活污水,反硝化污泥床去除有机物和硝态氮具有节省需好氧去除有机物的能耗的优势,同时好氧生物膜法硝化效率高。试验结果表明,当工艺进水的有机负荷小于2kgCOD/m3·d时,出水COD均小于60mg/L,好氧单元进水有机负荷和氨氮负荷分别小于13kgCOD/m3·d和09kgNH3N/m3·d时,出水氨氮小于5mg/L;COD/NO-3N是影响反硝化的关键因素,处理蔗糖配水时,COD/NO-3N大于5时反硝化脱氮完全,而COD/NO-3N为10时,生活污水作为电子供体仍然脱氮不完全;有机物含量过高导致好氧单元硝化效果降低,HRT是影响好氧单元硝化效率的主要因素,HRT缩短为15h时,氨氮去除率降低了85%左右;同时处理蔗糖配水和生活污水的反硝化菌活性相当。     

溅水充氧生物滤池处理农村污水的研究

开发了一种处理农村污水的低能耗地埋式一体化溅水充氧生物滤池装置,通过拔风和溅水复合充氧技术实现了大幅度节能条件下的好氧生物处理.考察了在不同水力负荷及COD、NH4 -N容积负荷条件下本装置的处理效果,结果表明,在水力负荷小于10 m3/(m2·d)、COD及NH4 -N容积负荷分别小于0.3 kg COD/(m3·d)和0.08 kg NH4 -N/(m3·d)的条件下,可以取得较高的去除效果和良好的出水水质,COD、NH4 -N和TN的平均出水浓度分别为58.94 mg/L、2.78 mg/L和8.23 mg/L,平均去除率分别为51.7%、86.4%和70.6%.     

颗粒污泥接种UASB反应器处理木糖醇废水试验研究

采用颗粒污泥接种UASB厌氧反应器处理木糖醇生产废水,对废水进行预调配后,由电控柜控制间歇进水.试验结果表明在进水COD为3～5g/L,COD容积负荷在2.70～4.64 kg/(m3·d)的范围时,有机污染物的去除率可稳定地保持在76%～88%,对厌氧出水再进行普通活性污泥法好氧后处理,出水COD可达到100 ms/L以下,稳定地达到国家要求的废水一级排放标准.     

双循环两相生物处理工艺的中试研究

采用双循环两相生物处理工艺(BICT)系统对城市污水处理厂出水进行中试研究,探讨了中试试验工况下BICT系统对污染物的去除率.结果表明,独立膜反应区的设置消除了生物硝化与除磷的关联性,从而可通过在SBR反应器缩短泥龄来提高系统的除磷效率;系统中污泥转移的实现,使系统在反应阶段能保证较高的污泥浓度,从而提高污泥的释磷效果,为系统处理能力的提升提供较大潜力.在适宜的试验工况下,进水COD容积负荷小于1.00 kg/(m3·d)时,系统COD平均去除率80%左右,出水COD保持在60 mg/L左右;总氮容积负荷小于0.4 kg/(m3·d)时,总氮平均去除率在80%左右,出水总氮低于15 mg/L;总磷容积负荷3～35 g/(m3·d)时,总磷去除率稳定在90%以上,出水总磷低于0.5 mg/L;出水指标均可达到<城镇污水处理厂污染物排放标准>(GB 18918-2002)中的一级标准.     

粉煤灰加气混凝土颗粒曝气生物滤池处理污水试验研究

在不同气水比、水力负荷条件下,应用粉煤灰加气混凝土颗粒曝气生物滤柱进行生活污水试验,结果表明,粉煤灰加气混凝土颗粒填料表面更易于形成硝化菌生物膜;兼顾处理效率与运行经济的最佳组合的气水比为2,水力负荷为30.72 m3/(m2·d).有机负荷保持在8.04～10.08 kg COD/(m3·d)之间,COD和NH3-N平均去除率分别达到74.2%和92%,出水COD、NH3-N平均浓度分别在60 mg/L和1 mg/L,达到GB18918-2002一级A标准,粉煤灰加气混凝土颗粒可以应用于曝气生物滤池处理污水工艺.     

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.     

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.     

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.     

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.