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1.
《Applied Geochemistry》1993,8(6):569-586
Crude oil floating on the water table in a sand and gravel aquifer provides a constant source of hydrocarbons to the groundwater at a site near Bemidji, Minnesota. The degradation of hydrocarbons affects the concentrations of oxidized and reduced aqueous species in the anoxic part of the contaminant plume that developed downgradient from the oil body. The concentrations of Fe2+, Mn2+ and CH4, Eh measurements, and the δ13C ratios of the total inorganic C indicate that the plume became more reducing ver a 5-a period. However, the size of the contaminant plume remained stable during this time. Field data coupled with laboratory microcosm experiments indicate that benzene and the alkylbenzenes are degraded in an anoxic environment. In anaerobic microcosm experiments conducted under field conditions, almost complete degradation (98%) was observed for benzene in 125 d and for toluene in 45 d. Concentrations of aqueous Fe2+ and Mn2+ increased in these experiments, indicating that the primary reactions were hydrocarbon degradation coupled with Fe and Mn reduction.Mass transfer calculations on a 40-m flowpath in the anoxic zone, downgradient from the oil body, indicated that the primary reactions in the anoxic zone are oxidation of organic compounds, precipitation of siderite and a ferroan calcite, dissolution of iron oxide and outgassing of CH4 and CO2. The major difference in the two models presented is the ratio of CO2 and CH4 that outgasses. Both models indicate quantitatively that large amounts of Fe are dissolved and reprecipitated as ferrous iron in the anoxic zone of the contaminant plume. 相似文献
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《Applied Geochemistry》1993,8(6):551-567
Crude oil spilled from a pipeline break in a remote area of north-central Minnesota has contaminated a shallow glacial outwash aquifer. Part of the oil was sprayed over a large area to the west of the pipeline and part of it accumulated in an oil body that floats at the water table to the east of the point of discharge. Total dissolved organic carbon (TDOC) concentrations in shallow groundwater collected in the oil spray area reach 16 mg/l. This is nearly an order of magnitude higher than the TDOC concentrations of native groundwater (∼2–3mg/l). The additional TDOC derives from the partial degradation of petroleum residues deposited at the land surface and transported to the aquifer by vertical recharge. In the vicinity of the oil body, TDOC concentrations in groundwater are 48 mg/l, 58% of the TDOC being composed of non-volatile organic C. The majority of the volatile DOC (63%) is a mixture of low-molecular-weight saturated, aromatic and alicyclic hydrocarbons derived from the oil. Downgradient from the oil body along the direction of groundwater flow, concentrations of all measured constituents of the TDOC pool decrease. Concentrations begin to decline most rapidly, however, in the zone where dissolved O2 concentrations begin to increase, ∼50m downgradient from the leading edge of the oil. Within the anoxic zone near the oil body, removal rates of isometric monoaromatic hydrocarbons vary widely. This indicates that the removal processes are mediated mainly by microbiological activity. Molecular and spectroscopic characterization of the TDOC and its spatial and temporal variation provide evidence of the importance of biogeochemical processes in attenuating petroleum contaminants in this perturbed subsurface environment. 相似文献
3.
Risk Assessment on Organic Contamination of Shallow Groundwater of an Oilfield in Northeast China 
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下载免费PDF全文 With the oil contaminated site of an oil field in northeast as the research area, based on the site geological and hydrogeological conditions, and by virtue of the methods of assessment on current situation of organic contamination and environmental impact assessment as well as leaching mobility assessment on organics, the internal and external risk assessments on organic contamination of shallow groundwater in the research area are conducted respectively. According to the results, about 30 kinds of organic components, including chlorinated hydrocarbons, mononuclear aromatics, heteroaromatic compound, polycyclic aromatic hydrocarbon and n-alkanes, are detected in the shallow groundwater in the research area. The current situation contamination of dichloromethane is the most serious, and all well points are of contamination at medium or above level. Compared with dichloromethane, contamination of trichloromethane and benzene is lighter, but several seriously contaminated well points occur in these two groups. The leaching mobility of dichloromethane, trichloromethane and benzene is extremely high, posing the greatest contamination risks against groundwater. 相似文献
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Pieter Jan Haest Richard Lookman Ilse Van Keer Johan Patyn Jan Bronders Marjan Joris Jan Bellon Florimond De Smedt 《Hydrogeology Journal》2010,18(8):1917-1925
The subsurface migration of methyl tertiary butyl ether (MTBE) and benzene towards a drinking-water production site in Belgium was monitored for 9 years. A large gasoline spill at a nearby fuel station had caused a 500-m long and 50-m-wide pollution plume of MTBE (10?30 mg/L) and benzene (2?10 mg/L). In order to prevent any intrusion of pollutants into the drinking-water supply, a conceptual model was used to design a pump-and-treat system that intercepted the gasoline-contaminated groundwater emanating from the spill. The contaminated soil in the spill zone was excavated. A numerical mass transport model was developed to evaluate the ongoing plume containment. The model describes the subsurface MTBE migration and was regularly updated, based on groundwater monitoring data and the measured mass of MTBE extracted with the pump-and-treat system. With continued interception pumping, the MTBE plume can be remediated in 14 years. Without it, MTBE and benzene concentrations up to 600 μg/L could have reached the drinking-water production site and the plume would persist for 9 years longer. Source zone treatment combined with plume interception pumping is a suitable risk-based remediation strategy for the containment of MTBE and benzene groundwater pollution. 相似文献
6.
《Applied Geochemistry》1999,14(5):655-667
Sediments sampled at a hydrocarbon-contaminated, glacial-outwash, sandy aquifer near Bemidji, Minnesota, were analyzed for sediment-associated Fe with several techniques. Extraction with 0.5 M HCl dissolved poorly crystalline Fe oxides and small amounts of Fe in crystalline Fe oxides, and extracted Fe from phyllosilicates. Use of Ti-citrate-EDTA-bicarbonate results in more complete removal of crystalline Fe oxides. The average HCl-extractable Fe(III) concentration in the sediments closest to the crude-oil contamination (16.2 μmol/g) has been reduced by up to 30% from background values (23.8 μmol/g) as a result of Fe(III) reduction in contaminated anoxic groundwater. Iron(II) concentrations are elevated in sediments within an anoxic plume in the aquifer. Iron(II) values under the oil body (19.2 μmol/g) are as much as 4 times those in the background sediments (4.6 μmol/g), indicating incorporation of reduced Fe in the contaminated sediments. A 70% increase in total extractable Fe at the anoxic/oxic transition zone indicates reoxidation and precipitation of Fe mobilized from sediment in the anoxic plume. Scanning electron microscopy detected authigenic ferroan calcite in the anoxic sediments and confirmed abundant Fe(III) oxyhydroxides at the anoxic/oxic boundary. The redox biogeochemistry of Fe in this system is coupled to contaminant degradation and is important in predicting processes of hydrocarbon degradation. 相似文献
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武汉市区第四系含水层地下水有机污染敏感性研究 总被引：14，自引：0，他引：14
在详细调查武汉市水文地质条件和地下水污染现状的基础上，获得了高精度的武汉市水环境中微量有机污染物的组成数据。所检测出的有机组分达30余种，以苯及相关苯系物为主，污染程度较高的地下水主要分布在人口密集区和工业，商业区，应用改进的DRASTIC模型－地下水污染敏感性评价模型，在GIS平台上，编制了武汉市区地下水污染敏感性分区图。根据其评价结果，建议集中对那些敏感性相对较高的区域采取有效的环保措施，开发利用时应作出风险评价。 相似文献
9.
Cüneyt Güler 《Environmental Earth Sciences》2009,59(3):631-643
This paper presents results from a site characterization and monitoring study at Karaduvar area (Mersin, SE Turkey), where
high concentrations of refined petroleum products have been detected in domestic and irrigation water wells. The saturated
and unsaturated zones in the deltaic aquifer are contaminated by large quantities of gasoline and diesel range fuel hydrocarbons
(GRHs and DRHs) released from diverse sources that include accidental spills, storage tank fires, pipeline breaks, deliberate
discharge of waste petroleum products from slop tanks and illegal tanker truck washing facilities. At the site, due to the
complex nature of the pollution sources, overlapping contaminant plumes exist and cover an area of about 0.5 km2. In both polluted and unpolluted parts of the aquifer, monitoring of groundwater physicochemical parameters in a total of
55 sampling points was carried out between 2006 and 2007. The results show that the terminal electron acceptors (e.g. dissolved
oxygen, nitrate, Mn(IV), Fe(III), sulfate) were reduced near the source area(s) indicating presence of actively operating
biodegradation processes at the site. Close to the contaminant source area(s), conditions in the plume are highly anoxic and
reducing; where high amounts of transformation products (e.g. bicarbonate, dissolved iron, and manganese) are present in solution.
Additionally, at the site, excessive pumping, careless land use, and deliberate wastewater discharges significantly deteriorated
the quality and quantity of groundwater. Excessive groundwater pumping for industrial and agricultural uses has resulted in
substantial water level declines (2–3 m) near the coastal part where seawater intrusion threatens the groundwater resources. 相似文献
10.
通过分析研究某农药化工企业密集区地下水水质及污染状况,按照国家有关标准,采用单指标评价法和内梅罗指数法对地下水的质量进行评价。评价结果显示：该区域地下水水质普遍较差,大部分为Ⅳ类及Ⅴ类水质,已不适于饮用。然后对该区域地下水污染进行评价,结果显示地下水有机和无机污染严重,并形成了以某农药化工企业为污染源并沿岩溶地下水流向的一个卤代烃类有机物污染羽,这表明造成该研究区岩溶地下水污染的主要污染源为某农药化工企业。最后根据评价结果,提出相应的控制地下水污染的建议和措施,为该地区制定地下水开发利用规划提供科学依据。 相似文献
11.
地下水微量有机污染 总被引：9，自引：1，他引：9
在简要评述其污染特征与研究特点的基础上，总结介绍了地下水微量有机污染的分布，污染物种类、性质、危害和来源，有机物的物化特征及其在环境中的迁移转化，以及污染控制技术。非极性难溶挥发性有机物（ＶＯＣ＇ｓ）是地下水中危害最大而又最为常见的有机污染物，主要由氯代脂肪烃（ＣＨＣ）和单环芳香烃（ＢＴＥＸ）构成。多数水溶相ＶＯＣ＇ｓ不易被吸附，在地下环境具有很强的迁移性，但在适当条件下可生物降解。非水溶相ＣＨＣ常在地下水中积聚潜伏于含水层底板，迁移不受地下水流向的控制；非水溶相ＢＴＥＸ则漂浮于地下水表面。非水溶相ＶＯＣ＇ｓ很难产生生物降解。ＶＯＣ＇ｓ的去除过程复杂，许多领域有待探索。 相似文献
12.
S. L. Shvartsev O. V. Serebrennikova M. A. Zdvizhkov O. G. Savichev O. S. Naimushina 《Geochemistry International》2012,50(4):367-380
New data are reported on the major- and trace-component compositions of acidic and weakly acidic low-concentration wetland
waters and other water types. Special attention was given to dissolved organic compounds: fulvic and humic acids, bitumens,
and hydrocarbons. The first comprehensive data are presented for organic trace components in the wetland waters of western
Siberia: alkanes, pentacyclic terpenoids, steranes, alkylbenzenes, naphthalenes, phenanthrenes, tetraarenes, etc. 相似文献
13.
当地下水邂逅DNA:石油类有机污染及其生物降解 总被引：1，自引：0，他引：1
地下水科学与工程研究发展到今日,已经成为一门涉及多个领域的综合性学科。地下水污染的控制和修复研究更需要跨学科的技术和知识支持,而生物修复作为一种高效低耗修复的技术成为环境领域的研究热点。微生物因其自身特性及其对污染的降解主导特征对确定有机物污染场地的永续修复具有重要意义。简要地综述了地下水有机污染及其原位修复、有机污染物和地下环境微生物的交互作用,进一步聚焦生物降解机制、生物修复和细菌研究。在此基础上以某石油污染场地地下水为例,进行了地下水中分离微生物菌株及其降解特征的实验研究。结果表明:放线菌降解效果最好,细菌和真菌次之;两两组合降解效果好于单菌,表明存在协同作用;不同菌株混合降解率较低,表明具有拮抗作用。通过动力学实验得出对TPH的降解符合一级反应动力学方程及其降解速度和降解半衰期。就微生物对有机组分降解而言,烷烃和总石油烃降解规律相似;难降解组分降解率低,后期因烷烃转化使其浓度升高;苯浓度变化不大。微生物活性实验表明:活菌总数和脱氢酶活性与降解率呈正相关变化。运用生理生化及分子生物学方法鉴定得出了具体的菌种。 相似文献
14.
Thamer Khazal Al-Ameri Afrah Hasan Al-Ekabi Sameer Noori Al-Jawad 《Arabian Journal of Geosciences》2014,7(4):1433-1455
Seventy-two core and cutting samples of the Ratawi Formation from selected wells of central and southern Iraq in Mesopotamian Foredeep Basin are analysed for their sedimentary organic matters. Dinoflagellates, spores and pollen are extracted by palynological techniques from these rocks. Accordingly, Hauterivian and late Valanginian ages are suggested for their span of depositional time. These palynomorphs with other organic matter constituents, such as foraminifer’s linings, bacteria and fungi, are used to delineate three palynofacies types that explain organic matter accumulation sites and their ability to generate hydrocarbons. Palaeoenvironments of these sites were mainly suboxic to anoxic with deposition of inshore and neritic marine environments especially for palynofacies type 2. Total organic matters of up to 1.75 total organic carbon (TOC) wt.% and early mature stage of up to 3.7 TAI based on the brown colour of the spore species Cyathidites australis and Gleichenidites senonicus with mottled interconnected amorphous organic matter are used for hydrocarbon generation assessment from this formation. On the other hand, these rock samples are processed with Rock-Eval pyrolysis. Outcomes and data calculations of these analyses are plotted on diagrams of kerogen types and hydrocarbon potential. Theses organic matter have reached the mature stage of up to T max?=?438 °C, hydrogen index of up to 600 mg hydrocarbons for each gram of TOC wt.% and mainly low TOC (0.50–1.55). Accordingly, this formation could generate fair quantities of hydrocarbons in Baghdad oil field and Basrah oil fields. Organic matters of this formation in the fields of Euphrates subzone extends from Hilla to Nasiriyah cities have not reached mature stage and hence not generated hydrocarbons from the Ratawi Formation. Software 1D PetroMod basin modelling of the Ratawi Formation has confirmed this approach of hydrocarbon generation with 100 % transformations of the intended organic matters to generate hydrocarbons to oil are performed in especially oil fields of East Baghdad, West Qurna and Majnoon while oil fields Ratawi and Subba had performed 80–95 % transformation to oil and hence end oil generation had charged partly the Tertiary traps that formed during the Alpine Orogeny. Oil fields of Nasiriyah and Kifle had performed least transformation ratio of about 10–20 % transformation to oil, and hence, most of the present oil in this field is migrated from eastern side of the Mesopotamian Foredeep Basin that hold higher maturation level. 相似文献
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太湖流域某地区浅层地下水有机污染特征 总被引：1，自引：0，他引：1
对太湖流域某地区浅层地下水有机污染特征进行了总结，并就污染来源、污染途径和典型污染源附近浅层地下水有机污染特征等问题进行了研究。研究结果表明，该地区浅层地下水中各组分的检出率较高，但检出浓度较低，除苯在个别采样点处超出美国环保局（EPA）饮用水标准外，其余卤代烃和单环芳烃组分均没有超标；平面分布上，卤代烃和单环芳烃各组分的浓度高值点大都集中于该地区东南部的工业区内，这种空间分布特征与工业区的分布具有明显的一致性；垂向上有浅部地下水的污染程度相对较重、深部地下水较轻的特点；典型污染源周边浅层地下水的污染程度较重，但随着采样点远离污染源，地下水中各有机污染组分的浓度迅速衰减。 相似文献
17.
苯、甲苯对粒状铁去除四氯乙烯影响的柱实验研究 总被引：2，自引：1，他引：1
挥发性氯代烃和石油烃类污染是地下水中最常见的混合污染类型,而且这两类污染物毒性极强,对人类危害非常严重。文中选取具有代表性的四氯乙烯、苯和甲苯为研究对象,采用柱实验的方法研究苯和甲苯在粒状铁反应系统中吸附平衡后,对粒状铁去除四氯乙烯的机理及反应动力学的影响。在实验装置运行的过程中,苯、甲苯和四氯乙烯的浓度始终控制在2mg/L左右的水平。实验结果表明:苯或甲苯的存在对被还原的产物组成没有影响,主要氯代中间产物均为TCE、1,1-DCE、cis-1,2-DCE和VC,但组成比例略有不同。苯和甲苯的存在对去除速率有影响,即苯对四氯乙烯的去除有促进作用,去除速率平均提高13.5%;而甲苯则抑制四氯乙烯的去除,去除速率平均降低13.8%。对比控制柱,苯和甲苯存在时对出水水化学变化的影响没有明显差异。 相似文献
18.
在系统分析柴达木盆地西部各油田40余个原油样品碳同位素和饱和烃、芳烃组成的基础上,全面剖析了该地区第三系湖相原油的地球化学特征.研究结果表明,这些原油具有特殊的碳同位素组成和异常的生物标志物分布.其全油碳同位素偏重(-26‰～-24‰);正构烷烃系列单体烃碳同位素分布曲线呈水平状,表现出类同于海相有机质的碳同位素组成特征.它们的生物标志物中正烷烃系列兼具奇碳和偶碳优势双重碳数分布模式;呈强植烷优势,Pr/Ph值大多<0.6;伽玛蜡烷普遍异常丰富,C35藿烷含量高,表征高盐、厌氧的咸水湖相沉积环境性质.芳烃组份以萘、菲系列为主,而二苯并噻吩等含硫有机化合物相对含量较低,反映该地区咸水湖相原油源岩沉积相的特殊性.柴西各油田原油地球化学参数在区域上呈规律性变化趋势,与其源岩沉积相的时空变迁相一致. 相似文献
19.
微生物降解是地下水中有机物自然衰减评估的关键,单体稳定同位素是一种有效的评估方法。在对某油罐泄露场地地下水流场识别的基础上,刻画不同地下水中污染物、微生物及电子受体特征,发现随着与污染源水力联系的减弱,污染物浓度明显减小,微生物群落结构和电子受体氧化还原作用类型与源相似的程度也逐渐减弱,呈现出“污染源-下游源区-下游污染羽-上游源区-侧翼污染羽”的空间变化规律。甲苯、间/对二甲苯碳的同位素标记结果发现,降解程度“侧翼污染羽﹥下游污染羽﹥下游源区”,与电子受体表征降解量的排序相反;该场地微生物降解符合一般化学反应“勒沙特列原理”:污染物浓度越高,降解量越大,但降解程度相对减小。 相似文献
20.
The objective of this study is to demonstrate the basic characteristics of Bacillus SP3 and evaluate its effect on different crude oils. Strain SP3 is a motile, gram-positive, spore-producing rod that was isolated from a reservoir of the Shengli oil field in East China. The cells of strain SP3 grew at high temperatures up to 58℃ at the pH range of 5.5–8.5. Strain SP3 grew facultatively and could use different organic substrates, and produce some metabolites such as 4-hydroxy-4-methyl-2-pentanone, methyl-2-nitrogen benzene and 1, 2-benzenedicarboxylic acid bis ester. Laboratory studies have demonstrated that the strain converted and degraded different components and changed the physical and chemical properties of crude oils. Strain SP3 degraded crude oil and the growth of bacteria on crude oil resulted in loss of aromatic hydrocarbons, resins and asphaltenes. The bioconversion of crude oils would lead to an enrichment in lighter hydrocarbons and an overall redistribution of saturate hydrocarbons. The interactions of microorganisms with crude oils are variable, depending on the microbial species and the chemical compositions of crude oils. 相似文献