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1.
农村生活污水处理技术的探讨   总被引:4,自引:0,他引:4  
刘洪喜 《污染防治技术》2009,22(3):30-31,78
农村的生活污水,是造成农村水环境污染的原因之一,也是造成湖泊富营养化的重要因素。针对中国农村生活污水排放分散、污染物浓度低的特点,介绍了生活污水净化沼气池技术、稳定塘生活污水处理技术、人工湿地处理技术、土地处理技术和生活污水地下自动连续处理技术等,以及几种工艺先进、具有推广价值的生活污水处理技术的原理、技术特点、适用条件以及工程应用实例,为农村地区污水治理提供参考。  相似文献   

2.
运用无动力人工湿地分散式处理农村生活污水的研究   总被引:2,自引:0,他引:2  
针对农村生活污水排放分散、难以集中处理等特点,以长沙市望城区光明村3户典型家庭为例,采用无动力人工湿地系统分散式处理农村生活污水,并比较冬、夏两季人工湿地对居民生活污水的净化效果。结果表明,构建的无动力人工湿地对农村生活污水净化效果明显,冬季生活污水COD、TP、TN、氨氮、SS的平均去除率分别达71.83%、97.20%、83.52%、55.34%、71.79%;夏季COD、TP、TN、氨氮、SS平均去除率分别达91.52%、93.99%、83.22%、75.15%、65.04%。经人工湿地净化处理后,TP、TN、氨氮可以达到《城镇污水处理厂污染物排放标准》(GB 18918—2002)一级A或一级B标准,COD可以达到GB 18918—2002二级标准,但人工湿地对COD及氨氮的去除受冬季低温影响十分显著,且出水SS不能达到GB 18918—2002相关标准,建议增加拦截设施或在冬季设置保温措施以提高人工湿地对农村生活污水的净化效果。  相似文献   

3.
针对单独应用Fenton氧化技术处理污泥的不足以及人工湿地在处理污水污泥方面的优势,以污水处理厂污泥浓缩池中含重金属污泥为对象,研究其依次经过Fenton氧化和人工湿地处理后重金属的去除效果及形态变化,以及污泥pH、TN和TP的变化情况。结果表明,Fenton氧化提高了污泥重金属的生物有效性,并促进了人工湿地对重金属的去除。Fenton氧化污泥经人工湿地处理后,Cu、Zn、Ni和Mn的去除率分别为67.2%、79.7%、37.0%和17.0%,与对照相比重金属的平均去除率提高了27.5%。经人工湿地处理后Fenton氧化污泥和原污泥重金属的生物有效性均降低。Fenton氧化污泥pH为4.4~4.6,经人工湿地处理后为6.2~7.1。人工湿地对Fenton氧化污泥和原污泥中TN的影响较小,而对TP表现出较高的去除率,2系统TP的去除率分别为51.1%和45.5%。  相似文献   

4.
农业面源污染是水体中COD、氮、磷等指标的主要来源。它包括农药化肥施用、畜禽养殖和农村生活污水排放。对农业源水污染物进行削减是实现污染物总量控制的重要手段。通过详细总结国内外现有农业源水污染物削减技术方法,分析对比其优缺点和实用性,筛选出适用于不同农业污染来源的污水处理技术。结果表明,畜禽养殖废水的适宜处理技术有厌氧/缺氧/好氧(A/A/O)、序批式活性污泥法(SBR)、膜生物反应器(MBR)、升流式厌氧污泥床(UASB)、厌氧沼气池;农地施肥污水的适宜处理技术有SBR、MBR、UASB;农村生活污水的适宜处理技术有厌氧沼气池、生物滴滤池、人工湿地、稳定塘。  相似文献   

5.
人工湿地在河道生态修复应用中的进展及优化   总被引:4,自引:0,他引:4  
认为人工湿地是河道生态修复的优选工艺,据此介绍了人工湿地在河道生态修复中的应用进展,并从构型、工艺组合、基质和植物四个方面进行了优化研究,结果表明:I-VFCW是构建人工湿地的优选构型;人工湿地与氧化塘、砂滤、接触氧化、絮凝沉淀等工艺组合,能够降低湿地堵塞的危险,提高处理能力;钢渣是除磷的优选基质,沸石是脱氮的优选基质;芦苇、香蒲、美人蕉等是优选植物。  相似文献   

6.
菖蒲人工湿地对城市生活污水的净化研究   总被引:2,自引:0,他引:2  
分别研究了土壤、粉煤灰和土壤及粉煤灰3种基质构建的菖蒲模拟人工湿地系统对城市生活污水的净化效果,并探讨了进水流量对城市生活污水净化效果的影响。结果表明,用粉煤灰基质构建的菖蒲模拟人工湿地系统的TP、TN、NH4+-N、浊度净化效果最佳,去除率最高,分别可达99.7%、85.8%、99.5%、99.3%;用粉煤灰和土壤基质构建的菖蒲模拟人工湿地系统的COD净化效果最佳,去除率最高,可达83.2%。因此,菖蒲人工湿地系统对城市生活污水的净化能力强,尤其适合广大中小城市生活污水的处理,具有极其广阔的应用与推广前景。  相似文献   

7.
针对太湖三山岛农村生活污水分布面广而分散和水质水量不稳定,以及三级处理费用高等问题,提出了人工湿地组合工艺。以设计规模为1 000 m3/d、处理生活污水的工艺系统为对象,探讨了氮元素在系统中的去除效果、途径及其一级去除速率常数。结果表明,该工艺对NH+4-N去除效果较好,出水NH+4-N平均达到地表水Ⅲ类,TN平均接近地表水Ⅴ类;潜流人工湿地、好氧生态塘C、兼性生态塘A和表流人工湿地D对氮的去除量分别占组合工艺去除总量的52.05%、18.65%、16.65%和12.65%;组合工艺对NH+4-N和TN的平均一级去除速率常数分比别为(14.47±2.01)和(25.91±4.99)m/a。  相似文献   

8.
为了研究新型多级复合人工湿地系统处理生活污水的除磷效果,分别对系统中COD、NH_4~+-N、TP的浓度和去除率进行分析。结果表明,最终出水COD、NH_4~+-N、TP浓度分别低于30、4.1和0.17 mg·L~(-1),去除率最高达到70.40%、71.0%和95.5%。工艺由前置系统、多级复合流湿地系统、后置氧化塘系统组成,每部分TP的去除率约占系统总去除率的6%、79%和15%,多级复合流湿地系统每级TP的去除率在15%~20%。出水中各类污染指标长期达到GB18918—2002一级A标准,TP最低出水浓度为0.075 mg·L~(-1),工艺除磷效果好。新型多级复合人工湿地布水均匀、不易堵塞,灵活度高,投资少,运行稳定、管理简单,可作为农村生活污水除磷的有效方法。  相似文献   

9.
表面水力负荷对锰渣陶瓷球填料人工湿地的影响研究   总被引:1,自引:0,他引:1  
云贵高原地区农村面源污染严重。参照贵州铜仁农村面源污水配制模拟污水,研究了表面水力负荷对锰渣陶瓷球填料人工湿地的影响。结果表明,该人工湿地的最佳表面水力负荷为0.55m~3/(m~2·d),此时COD、氨氮、硝态氮和TP去除率分别为90.12%、76.45%、70.04%、87.48%。以锰渣陶瓷球代替砾石作为人工湿地填料能显著提高人工湿地对污染物的去除能力。  相似文献   

10.
人工湿地作为一种新型污水生态处理工艺受到越来越广泛的重视,在生活污水、特种工业废水、采矿污水、农业和畜牧业污水以及水产养殖废水等处理中得到了广泛的应用.但是其本身的局限却限制了它在高浓度废水、某些工业废水处理等方面的应用,在寒冷地区的应用也受到限制.本研究分析了一些强化技术(如湿地内部要素强化、工艺强化和工程强化等)在提高人工湿地的净化效能以及扩大其应用范围的可能性.  相似文献   

11.
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.  相似文献   

12.
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.  相似文献   

13.
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.  相似文献   

14.
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.  相似文献   

15.
16.
Approximately 25, 000-35, 000 dry cleaning facilities currently operate in the U.S. The release of perchloroethylene and other solvents from these establishments represents a major source of soil and groundwater contamination. The manner in which dry cleaning solvents escape from dry cleaning plants is, for all practical purposes, identical for chlorinated and petroleum hydrocarbon solvents and is related to one of the following events: the catastrophic failure of a component of the dry cleaning system, the improper installation, operation or maintenance of the dry cleaning equipment or a combination of all of these causes. Acceptable customs, codes and regulations can also dictate what is authorized for operation of a dry cleaning facility in a particular community, geographic area during a particular time frame. Environmental litigation dealing with the origin of a solvent release from dry cleaners tends to focus on the design and manufacture of dry cleaning industry machines such as washers, washer extractors, tumblers, solvent filters, water separators, stills and spotting boards. A thorough analysis of the daily operations of dry cleaners often reveals that poor maintenance, failure to follow the manufacturer's instructions and the actions of the operator are the most likely causes of soil and groundwater pollution. In order to forensically evaluate the most probable origins of a solvent release and to examine issues regarding liability, a thorough understanding of the history of dry cleaning and a detailed analysis of the operation and maintenance of the dry cleaning equipment are necessary. The discovery of solvent plumes in the vicinity of dry cleaning plants may suggest that the solvent source is the dry cleaning plant; however, the presence of these plumes does not necessarily indicate that the dry cleaning equipment was defectively designed or manufactured. A thorough review of the type of equipment used over the life of the dry cleaning plant and verifiable solvent mileage records frequently indicates that operators of the plant have disposed of solvent and contaminated solids into the municipal sewer or on ground surfaces.  相似文献   

17.
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.  相似文献   

18.
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.  相似文献   

19.
Organochlorine compounds in a three-step terrestrial food chain   总被引:1,自引:0,他引:1  
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.  相似文献   

20.
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.  相似文献   

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