造纸中段废水与生活污水合并深度处理工艺

采用水解酸化 CAST 混凝 复合滤池与水解酸化 接触氧化 混凝 复合滤池2种组合工艺对造纸中段废水与生活污水进行合并处理对照试验.结果表明,两种工艺都是切实可行的,二级出水均可达到<污水综合排放标准>(GB8978-1996)二级标准,深度处理出水可达中水水质要求.其中以水解酸化 CAST 混凝 复合滤池组合工艺效果最好.     

印染废水处理过程中污染物及毒性分析

应用水解酸化-A/O(生物活性炭法(PACT))-混凝沉淀组合工艺处理印染废水,深入研究该组合工艺各反应段对印染废水污染物的处理情况,分别用电感耦合等离子光谱(AES/ICP)、气相色谱/质谱联用(GC/MS)以及发光细菌法对各反应段出水所含金属元素、有机物以及毒性进行检测.结果表明,水解酸化-A/O(PACT)-混凝沉淀组合工艺可以有效降解印染废水所含污染物,降低其毒性.     

低能耗印染废水处理工艺与运行条件

采用UASB反应器+三段好氧+混凝沉淀组合工艺处理印染工业园废水。结果表明,工程运行中,通过导流墙的设置,UASB水解酸化反应器的运行以及运行工况的控制,在出水稳定在《城镇污水处理厂污染物排放标准》(GB18918—2002)一级A标准时,该系统处理每吨污水电费为0.36元。     

生物法/人工湿地工艺处理采油废水及其生态毒性削减研究

采用2种生物法/人工湿地工艺(水解酸化/好氧/人工湿地工艺和水解酸化/人工湿地(进水区强化曝气)工艺)处理胜利油田某联合处理站经隔油、混凝处理的采油废水,并运用发光细菌技术研究采油废水在处理过程中的生态毒性削减规律.研究结果表明,在水解酸化段水力停留时间(HRT)为20 h,好氧段HRT为10 h,人工湿地HRT为2 d的工况下,水解酸化/好氧/人工湿地工艺与水解酸化/人工湿地(进水区强化曝气)工艺的出水水质均能满足COD≤80 mg/L、NH_4~+-N≤15 mg/L的处理要求.发光细菌法试验结果表明,经隔油、混凝处理后的采油废水属高毒性废水,再经水解酸化/人工湿地(进水区强化曝气)工艺处理后生态毒性大幅削减,出水生态毒性降至低毒.     

AOAB工艺处理难降解混合化工污水的挂膜启动

采用AOAB(水解酸化A1+生物接触氧化O+深度水解酸化A2+曝气生物滤池BAF)工艺处理难降解混合化工污水,重点研究工艺挂膜方式和生物膜的驯化。结果表明,采用分段连续式挂膜法进行反应器挂膜,20 d即可完成快速挂膜启动;采用分阶段同步培养驯化法驯化生物膜,30 d内可完成高浓度多组分混合化工污水进水的驯化,最终进水COD 1 456 mg/L,出水COD 324 mg/L,总去除率76.85%,驯化效果显著;整个工艺对COD的降解主要集中在生物接触氧化池和曝气生物滤池,驯化期间生物接触氧化池去除率稳定在40%左右,曝气生物滤池去除率稳定在50%以上。同时,通过对比一段水解酸化和深度水解酸化的VFA(挥发性脂肪酸)产出,表明在高有机负荷进水时,一段水解酸化降解大分子有机物的能力有限,但这些有机物可通过二段水解酸化再次降解,由此体现了AOAB工艺在处理多组分混合型的难降解化工污水的优势。     

低污泥产量印染废水处理工艺与运行条件

采用UASB反应器+三段好氧+混凝沉淀组合工艺处理印染工业园废水,对污泥减量化进行探索。结果表明,工程运行中,通过控制运行参数、以及运用UASB水解酸化反应器及生物捕食技术,在出水稳定在《城镇污水处理厂污染物排放标准》(GB18918-2002)一级A标准时,该系统处理每吨污水污泥产量为1 046 g。     

硫酸卷曲霉素生产废水生化前预处理试验研究

对某厂硫酸卷曲霉素废水进行预处理试验,为水处理工程设计提供参考.选择混凝-气浮-水解酸化工艺组合作为预处理工艺,试验表明,依某厂硫酸卷曲霉素生产废水特征,以PAC为混凝剂、PAM为助凝剂,投药量分别为100和5 mg/L条件下,混凝-气浮单元的COD、BOD5和SS去除率分别在42.6%～48.7%、25.5%～40.8%和84.6%～92.6%之间;在水解酸化单元接种厌氧污泥,可以大大缩短污泥驯化时间,用经过14 d驯化时间的污泥处理气浮单元出水,HRT为16 h时,该单元的COD、BOD5去除率分别在8.4%～33.8%和5.0%～19.5%之间;气浮单元、水解酸化单元均提高了出水的可生化性.将混凝-气浮单元与水解酸化单元联合作为硫酸卷曲霉素生产废水的生化处理的前处理措施是可行的.     

混凝-折流式反应器对垃圾渗滤液处理的试验研究

采用混凝、三组水解池和好氧生物滤池串连组成的折流式反应器(BR)联合工艺,对处理芜湖市南郊垃圾填埋场产生的渗滤液进行了试验研究,确定了混凝剂的最佳投加量、最佳碱化脱氮pH等工艺参数.试验结果表明,经过水解反应器(HUSB)反复对垃圾渗滤液进行水解酸化后,能逐步提高废水的BOD5/COD(B/C)(约0.2～0.4),大大提高了好氧生物滤池的COD容积负荷,出水COD平均《400 mg/L,NH3-N平均《30 mg/L.     

混凝—水解酸化—好氧工艺处理印染废水的设计与运行

采用混凝-水解酸化-好氧工艺处理印染废水,设计规模3000m3/d.当进水C0D在571～1752 mg/L时,处理后的出水可达国家<污水综合排放标准>(GB 8978-1996),主要污染物ρ(C0D)＜100mg/L.     

混凝-水解酸化-好氧-混凝工艺处理印染废水

采用“混凝-水解酸化-好氧-混凝”工艺处理印染废水，当进水COD为800—1200mg／L时，出水可达到国家《污水综合排放标准》（GB1978--1996），其中COD指标甚至达到江苏地方标准《太湖地区城镇污水处理厂及重点工业行业主要水污染物排放限值》（DB32／T1072--2007）。     

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.     

Radionuclides and trace elements in fish collected upstream and downstream of Los Alamos national laboratory and the doses to humans from the consumption of muscle and bone

Abstract

The purpose of this study was to determine radionuclide and trace element concentrations in bottom‐feeding fish (catfish, carp, and suckers) collected from the confluences of some of the major canyons that cross Los Alamos National Laboratory (LANL) lands with the Rio Grande (RG) and the potential radiological doses from the ingestion of these fish. Samples of muscle and bone (and viscera in some cases) were analyzed for ³H, ⁹⁰Sr, ¹³⁷Cs, ^totU, ²³⁸Pu, ^239,240Pu, and ²⁴¹Am and Ag, As, Ba, Be, Cr, Cd, Cu, Hg, Ni, Pb, Sb, Se, and Tl. Most radionuclides, with the exception of ⁹⁰Sr, in the muscle plus bone portions of fish collected from LANL canyons/RG were not significantly (p<0.05) higher from fish collected upstream (San Ildefonso/background) of LANL. Strontium‐90 in fish muscle plus bone tissue significantly (p<0.05) increases in concentration starting from Los Alamos Canyon, the most upstream confluence (fish contained 3.4E‐02 pCi g^‐1 [126E‐02 Bq kg^‐1]), to Frijoles Canyon, the most downstream confluence (fish contained 14E‐02 pCi g^‐1 [518E‐02 Bq kg^‐1]). The differences in ⁹⁰Sr concentrations in fish collected downstream and upstream (background) of LANL, however, were very small. Based on the average concentrations (±2SD) of radionuclides in fish tissue from the four LANL confluences, the committed effective dose equivalent from the ingestion of 46 lb (21 kg) (maximum ingestion rate per person per year) of fish muscle plus bone, after the subtraction of background, was 0.1 ± 0.1 mrem y^‐1 (1.0 ± 1.0 μSv y^‐1), and was far below the International Commission on Radiological Protection (all pathway) permissible dose limit of 100 mrem y^‐1 (1000 μSv y^‐1). Of the trace elements that were found above the limits of detection (Ba, Cu, and Hg) in fish muscle collected from the confluences of canyons that cross LANL and the RG, none were in significantly higher (p<0.05) concentrations than in muscle of fish collected from background locations.     

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.     

Sorption and predicted mobility of herbicides in Baltic soils

This study was undertaken to determine sorption coefficients of eight herbicides (alachlor, amitrole, atrazine, simazine, dicamba, imazamox, imazethapyr, and pendimethalin) to seven agricultural soils from sites throughout Lithuania. The measured sorption coefficients were used to predict the susceptibility of these herbicides to leach to groundwater. Soil-water partitioning coefficients were measured in batch equilibrium studies using radiolabeled herbicides. In most soils, sorption followed the general trend pendimethalin > alachlor > atrazine～ amitrole～ simazine > imazethapyr > imazamox > dicamba, consistent with the trends in hydrophobicity (log K_ow) except in the case of amitrole. For several herbicides, sorption coefficients and calculated retardation factors were lowest (predicted to be most susceptible to leaching) in a soil of intermediate organic carbon content and sand content. Calculated herbicide retardation factors were high for soils with high organic carbon contents. Estimated leaching times under saturated conditions, assuming no herbicide degradation and no preferential water flow, were more strongly affected by soil textural effects on predicted water flow than by herbicide sorption effects. All herbicides were predicted to be slowest to leach in soils with high clay and low sand contents, and fastest to leach in soils with high sand content and low organic matter content. Herbicide management is important to the continued increase in agricultural production and profitability in the Baltic region, and these results will be useful in identifying critical areas requiring improved management practices to reduce water contamination by pesticides.