城市生活垃圾填埋场渗滤液生化处理过程中重金属离子问题

我国对城市生活填埋场渗滤液处理技术的研究主要集中在COD与NH4 -N的去除上,对渗滤液中重金属离子的专项研究几乎未见报道.本文首先总结了国内外城市生活垃圾渗滤液中重金属的种类及浓度,在渗滤液中的存在状态,渗滤液中重金属与其他成分(有机物、氨氮)的相互作用关系,辨证分析了重金属在渗滤液生化处理过程中的有益作用和毒性,归纳了重金属在渗滤液生化处理过程中的变化规律,同时总结分析了重金属的去除技术.     

pH对电解处理垃圾渗滤液的影响

在不同的pH值条件下对氯离子和重金属离子含量不同的渗滤液和邻硝基苯酚人工模拟废水进行了电解处理,着重考察了不同pH值条件下氯离子浓度和重金属离子种类对有机物电解去除效果的影响。结果表明,电解处理过程中, pH值对有机物电解去除效果的影响与渗滤液的水质有关,尤其与渗滤液中氯离子和重金属离子浓度以及重金属离子种类有关。在pH＝2的条件下电解处理氯离子和重金属离子含量均很低的渗滤液,有利于有机物的氧化去除;在pH=9的条件下电解处理氯离子和重金属离子浓度均较高的渗滤液,其COD的电解去除效果最好;在pH=2或pH=12的条件下电解处理氯离子浓度高而重金属离子浓度低的渗滤液,能促进有机物的氧化分解。在一定浓度范围内,渗滤液中无机变价离子的组成不同,电解处理垃圾渗滤液的最佳pH值也不同。     

城市生活垃圾焚烧厂渗滤液产甲烷潜力

为研究城市生活垃圾焚烧厂渗滤液的产甲烷潜力及其影响因素,在常规水质分析的基础上,采用瑞典AMPTSⅡ系统进行中温((37±1) ℃)厌氧消化实验,探究稀释倍数和污泥投加量对城市生活垃圾焚烧厂渗滤液的甲烷产率和可生物降解性的影响。结果表明：城市生活垃圾焚烧厂渗滤液的甲烷产率(以CH4/CODadd计)高于326.0 mL·g-1(理论甲烷产率为350 mL·g-1),可生物降解性高于93.1%;城市生活垃圾焚烧厂渗滤液是一种高COD、高NH3-N的有机废水,但可生化性较好;无论污泥投加量还是稀释倍数对城市生活垃圾焚烧厂渗滤液的甲烷产率和可生物降解性影响都很小,但稀释倍数的增加可明显降低污泥驯化时间和厌氧消化时间。在工程应用中,采用生化出水回流稀释城市生活垃圾焚烧厂渗滤液的方法,可降低厌氧反应器启动时间和厌氧消化时间,提高城市生活垃圾焚烧厂渗滤液处理效率。     

AS-SMBR工艺处理垃圾渗滤液实验研究

采用AS-SMBR工艺处理城市生活垃圾填埋场渗滤液,选择DO 2～4 mg/L、HRT50～60 h,在常温环境下运行结果表明:AS-SMBR工艺对垃圾渗滤液中COD和氨氮具有高效的去除效果,COD总去除率在50%～60%,NH3-N去除效率在95%以上;COD和NH3-N运行负荷分别为0.2～0.3 kg COD/(kg MLSS.d)和0.06～0.18 g NH3-N/(g MLSS.d);垃圾渗滤液生化系统对大分子物质的降解程度对膜去除效率有重要影响,两者对COD去除效率呈现波浪式交替变化。     

超声去除垃圾渗滤液中的氨氮

采用超声辐照技术去除垃圾渗滤液中的氨氮.研究结果表明,超声辐照对垃圾渗滤液中的氨氮有很好的去除效果.渗滤液中氨氮超声去除的机理主要是氨氮以游离氨的形式在空化泡内发生高温热解反应,生成氮气和氢气而排出.     

超声去除垃圾渗滤液中的氨氮

采用超声辐照技术去除垃圾渗滤液中的氨氮.研究结果表明,超声辐照对垃圾渗滤液中的氨氮有很好的去除效果.渗滤液中氨氮超声去除的机理主要是氨氮以游离氨的形式在空化泡内发生高温热解反应,生成氮气和氢气而排出.     

磷酸铵镁沉淀法去除垃圾渗滤液中氨氮的实验研究

叙述了磷酸铵镁沉淀法(MAP法)去除垃圾渗滤液中氨氮的基本原理,分析了MAP法对氨氮的去除效果及其产物中的重金属含量,对比了不同的镁盐及不同的反应时间对氨氮的去除效率.结果表明,该方法对氨氮的去除效率高,产物中重金属的含量低.同时,选择MgO比选择MgCl2具有更好的氨氮去除综合优势,理想的氨氮去除条件为pH=9.5,Mg:N:P=1:1:1.     

环境污染治理技术与设备2006年(第7卷)总目次

综合评述城市生活垃圾填埋场渗滤液生化处理过程中重金属离子问题……………………………………彭永臻张树军郑淑文王淑莹1(1)廉价吸附剂处理重金属离子废水的研究进展……………………………………………………………………………李增新薛淑云1(6)微囊藻毒素污染控制技术的研究进展……………………………………………………陈一萍苑宝玲李艳波刘会娟曲久辉1(12)粘土矿物与重金属界面反应的研究进展…………………………………………………………………………………刘云吴平霄1(17)污水土壤含水层处理系统原理、管理、效率和应用………………     

物理化学法处理垃圾填埋场渗滤液的研究进展

本文介绍了渗滤液的特性，指出物理化学法是渗滤液处理过程中不可缺少的环节。总结了物理化学法处理渗滤液的进展状况，并提出了物理化学法处理渗滤液存在的问题及未来发展趋势。     

城市生活垃圾填埋场渗滤液处理方案探讨

对垃圾填埋场渗滤液水处理工艺方案及相关技术进行了分析，针对合并处理与单独处理方案本身存在的问题，提出以渗滤液回灌技术作为合并处理中预处理工艺，削减单独处理方案中生化负荷并加速渗滤液水质稳定化的设想。     

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.     

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.     

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.     

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.