生活垃圾填埋场对地下水污染的风险评价——以北京北天堂垃圾填埋场为例

以国外生活垃圾填埋场对地下水污染的风险评价方法为基础,建立了综合考虑含水层脆弱性及生活垃圾填埋场自身性质的地下水污染风险评价方法,并以北京北天堂垃圾填埋场为例.评价了当地4个生活垃圾填埋场对地下水污染的风险级别.结果表明,生活垃圾填埋场对地下水污染的风险取决于场地规模、防护情况等自身相关参数以及场地所处位置的含水层脆弱...     

基于文献计量的垃圾填埋场污染物研究现状与趋势分析

基于Web of Science核心合集数据库，利用VOSviewer和CiteSpace软件，对2000—2020年有关垃圾填埋场污染物的文献进行了计量分析。结果表明：(1)2000—2020年，垃圾填埋场污染物领域的发文量总体呈逐年增加态势，2015年后中国的发文量直线上升；(2)中国的机构虽然发文量多，但均篇被引频次不是很高，影响力还有待进一步提升；(3)垃圾填埋场污染物研究的热点包括城市固体废弃物及其处置过程，垃圾渗滤液或污废水中有机污染物的去除、降解，垃圾填埋场周边地表水和地下水中污染物的环境行为，无机污染物氮元素的去除，垃圾填埋场中新污染物的环境行为和去除5大类；(4)垃圾填埋场污染物主要分为重金属和有机污染物两大类，其中重金属在不同环境介质中出现的频次高于有机污染物，填埋气等气态污染物造成的环境问题也不容忽视。     

基于层次分析法的坦塘垃圾填埋场适宜性评价

垃圾填埋场场址的适宜性评价是生活垃圾填埋场建设和运营的前提和基础。以湖南省永州市坦塘垃圾填埋场为例,在分析研究区的地质与水文地质条件的基础上,确定了填埋场适宜性的影响因素为填埋场规模、运输条件、环境条件、建场条件和地质条件,具体包括填埋场面积及容量、综合路况条件、对地表水体污染的可能性、地形平坦程度以及场地是否处在岩溶区等条件,明确了局部地区岩溶发育是制约其适宜性的主要因素。结合垃圾填埋场的建设情况和相关规范、标准,采用层次分析法对坦塘垃圾填埋场进行适宜性评价。评价结果表明,坦塘垃圾填埋场是一个适宜场地,评价结果与实际情况相符。     

贵州某垃圾填埋场及其附近农田土壤中重金属形态分析和评价

对贵州某垃圾填埋场及其附近农田土壤中Cu、Zn、Cr、M n、Pb、Cd 6种重金属的总量和形态进行了分析,并计算了内梅罗综合污染指数,评价了健康风险和生态风险.结果表明:(1)贵州某垃圾填埋场及其附近农田土壤中Cd、Cr、Cu、Zn、Pb和Mn的质量浓度平均值分别为0.44、192.89、45.68、264.39、3...     

原位回灌对垃圾填埋场稳定化进程影响的实验研究

针对填埋法处理城市生活垃圾造成的土地占用和水资源污染等系列环境问题,通过在实验室搭建的模拟城市生活垃圾填埋场实验台,系统研究了淋滤介质、淋滤量和淋滤频率等条件对生活垃圾填埋场稳定化进程的影响。结果表明:采用垃圾渗滤液原液淋滤、淋滤频率为3次/d、淋滤总量为10L时,垃圾填埋场初期稳定化进程最快;在此条件下,垃圾渗滤液中污染物COD、氨氮和TP出现负增长对应的时间分别为17、29、18d。研究结果对进一步开展垃圾渗滤液深度处理和工程应用等相关研究具有重要的指导意义。     

垃圾降解过程中淀粉酶活性测定条件优化

垃圾填埋场中垃圾降解初期,淀粉酶活性对于垃圾填埋场中碳素的转化过程和垃圾填埋场生物学特性的研究有重要意义,而且也可作为垃圾填埋场稳定化机制研究的重要指标之一.以模拟垃圾填埋系统的垃圾为研究对象,通过正交实验(L25(56))对淀粉酶活性的测定条件进行了优化研究.结果表明:(1)正交实验结果表明,对淀粉酶活性测定的影响大...     

城市垃圾卫生填埋场废气产生量及主要污染因子的确定

城市生活垃圾以其特有的分散、巨量、恶臭、肮脏等特性,使环境污染问题显得更加突出、复杂,因此建造垃圾填埋场势在必行。本文以城市垃圾卫生填埋场址的环境影响评价为基础,对垃圾填埋场恶臭气体产生量及其影响强度进行科学的分析与探讨,为垃圾场废气的治理及环境管理提供科学依据。1　垃圾卫生填埋废气产生量分析1.1　废气污染物的产生及特征根据有关实验及文献资料〔1,2〕,填埋场中废气大致由50%～60%的CH4,40%～50%的CO2和一定量的NH3、N2、H2S等物质组成。填埋场产生的废气成份应根据生产过程来确定,在填埋初期两周内氮、氧的含量比…     

填埋场沼气发电的温室气体减排效益分析

填埋场沼气是垃圾卫生填埋场产生的可利用资源.以深圳下坪垃圾填埋场为例,定量分析垃圾填埋气体发电的温室气体减排效益.结果表明,填埋场沼气发电具有很好的经济效益和环境效益,可作为与发达国家进行CDM(清洁发展机制)项目合作的优先技术领域.     

垃圾填埋场对地下水污染的模拟研究

在对长春市某垃圾填埋场进行野外调查的基础上，于室内进行了垃圾淋滤模拟实验。分析了垃圾渗滤液污染组分的自然衰减规律，建立了垃圾填埋场地下水污染的数值模型，采用FEFLOW软件对其进行模拟和预报，并取得了较好的效果，最后提出防止和防治垃圾填埋场污染地下水的若干措施。     

垃圾填埋场对地下水污染的模拟研究

在对长春市某垃圾填埋场进行野外调查的基础上 ,于室内进行了垃圾淋滤模拟实验。分析了垃圾渗滤液污染组分的自然衰减规律 ,建立了垃圾填埋场地下水污染的数值模型 ,采用FEFLOW软件对其进行模拟和预报 ,并取得了较好的效果 ,最后提出防止和防治垃圾填埋场污染地下水的若干措施。     

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.