首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 31 毫秒
1.
2.
Monitored natural attenuation can be a viable option for remediation of groundwater contamination by BTEX compounds. Under the field conditions, the rate of contaminant mass attenuation through natural processes, such as biodegradation, to a large extent affected by the groundwater flow regime, which is primarily controlled by the aquifer heterogeneity. Numerical simulation techniques were used to describe quantitatively the relationship between biodegradation rate of BTEX and aquifer heterogeneity. Different levels of aquifer heterogeneity were described by random hydraulic conductivity fields (K) having different statistical parameters, the coefficient of variation (CV) and the correlation length (h). The Turning Bands Algorithm was used to generate such K fields. Visual MODFLOW/RT3D was used to simulate the fate and transport of dissolved BTEX plume within heterogeneous aquifers. The multispecies reactive transport approach described BTEX degradation using multiple terminal electron-accepting processes. First-order biodegradation rate constants were calculated from simulated BTEX plumes in heterogeneous flow fields. The results showed that aquifer heterogeneity significantly affected biodegradation rate; it decreased with increasing CV when h was in the range of up to 12 m, whereas it increased with increasing CV when h was greater than about 12 m. For well characterized aquifers, this finding could be of great value in assessing the effectiveness of natural attenuation during feasibility studies at BTEX contaminated sites.  相似文献   

3.
 Contamination of groundwater by petroleum-hydrocarbons is a widespread environmental problem. Natural attenuation is a passive remedial approach to degrade and dissipate contaminants in soil and groundwater. In this study, a mass flux approach was used to calculate the contaminant mass reduction and field-scale decay rate at a gasoline spill site. The mass flux technique is accomplished using the differences in total contaminant mass flux across two cross sections of the contaminant plume. The mass flux calculation shows that up to 88% of the dissolved BTEX (benzene, toluene, ethylbenzene, and xylene isomers) removal was observed by natural attenuation processes. The efficiency of intrinsic biodegradation was evaluated by the in situ tracer method. A first-order decay model was applied for the natural attenuation and intrinsic biodegradation rate calculation. Results reveal that intrinsic biodegradation process was the major cause of the BTEX reduction among the natural attenuation mechanisms, and iron reduction was the dominant biodegradation pattern within the plume. Approximately 87% of the BTEX removal was caused by intrinsic biodegradation processes. The calculated BTEX natural attenuation and intrinsic biodegradation rates were 0.24 and 0.16% l/day, respectively. Results suggest that natural attenuation mechanisms can effectively contain the plume, and the mass flux method is useful in assessing the efficiency of the natural attenuation. Received: 6 December 1999 · Accepted: 11 July 2000  相似文献   

4.
In order to find out the distribution characteristics of BTEX in groundwater, which include Benzene, Toluene, Ethylbenzene, p-Xylene, m-Xylene, and o-Xylene, 82 groups of groundwater samples and 10 surface water samples collected from Guangzhou in Guangdong during 2005 to 2008 were tested by gas chromatography and mass spectrum(GC/MS). The result showed that the BTEX concentration in groundwater does not exceed the standard. The detection rate of BTEX is 14.63% in groundwater, and the total BTEX concentration is lower than 9.5 μg/L. Of 6 kinds of BTEX, toluene had the highest detection rate(12.20%) and detection value(9.5 μg/L), which was followed by Benzene, with the detection rate of 3.65%, and detection value of 4.9 μg/L respectively; most of samples with BTEX are distributed in Huangpu district, Baiyun district, Huadu district and other industrialized areas; this spatial distribution and urban distribution have obvious consistency. With economic development, plant expansion and population growth led to a large amount of waste water discharge, and infrastructure construction is lagging behind, indicating that rapid urbanization is a major driving force of BTEX in groundwater, and through the analysis of a typical area, it is found that benzene system surface water infiltration was an important source of BTEX in groundwater of Guangzhou.  相似文献   

5.
汽油污染含水层中芳香烃的自然去除与生物降解特征   总被引:7,自引:0,他引:7  
石油烃污染地下水是一个普遍而严重的环境问题.用砂卵石、中粗砂、细砂、粉砂和粘土等在实验室内按照自然界沉积物层序制作了一个含水层物理模型,具有给水、排水、监测、抽提、淋滤与注入等功能.利用该模型开展石油烃污染地下水的特征研究结果表明,苯、甲苯、乙苯和二甲苯(benzene,toluene,ethylbenzene,xylene;BTEX)各溶解组分能够被自然去除,其中甲苯自然衰减的速率系数为0.057 5~0.150 4 d-1,二甲苯为0.068 3~0.104 6 d,乙苯大约为0.047 8 d,苯为O.017 8~0.040 6 d.甲苯与二甲苯容易被去除,然而苯的去除则需要较长的时间.作为BTEX去除反应的电子受体,溶解氧、硝酸盐在需氧或厌氧条件下具有优先利用的机会,而硫酸盐则缺乏优先利用的机会.BTEX溶解组分浓度的降低,加上电子受体浓度的降低,可以表明含水层存在需氧条件与硝酸盐还原条件下的内在生物降解作用.其意义在于通过增加含水层中电子受体的浓度,将有助于内在生物降解能力的增强,从而能够提高含水层中污染物去除的效果.  相似文献   

6.
A previously developed two-dimensional numerical model is further developed for simulating the transport of dissolved contaminants originating from dissolution of a coal tar pool in a stratified, saturated porous medium. The model is used to simulate contaminant transport resulting from a rectangular-shaped coal-tar-pool dissolution experiment conducted in a large-scale experimental aquifer. The experimental porous medium consists of two sand strata, a high-hydraulic-conductivity upper stratum and a low-hydraulic-conductivity bottom stratum. The experiment was conducted to a time of 354 days and the groundwater velocity was changed several times within this duration. Model simulations show good agreement against observed contaminant concentrations, and simulations show that dissolved solute below the pool migrated deeper into the bottom stratum as compared to the upper stratum. Furthermore, simulations also suggest that contaminant concentrations in the lower stratum never reached quasi steady-state during the experimental time frame.  相似文献   

7.
    岩溶含水系统遭受石油烃污染的环境问题十分普遍。相对于多孔含水介质,石油烃BTEX在石灰岩含水介质中的生 物可降解性还不确定。为此,本研究开展了BTEX在石灰石和岩溶地下水介质中的静态微元体实验。经过77天的实验检测 分析,结果表明:(1) BTEX化合物在可利用电子受体溶解氧或硝酸盐存在条件下具有生物可降解性;(2) 向系统中补充 电子受体硝酸盐,具有促进生物降解的作用,其对BTEX的去除率可高达94%;(3) 未发现补充硫酸盐能够促进BTEX生物 可降解性;(4) 甲苯和二甲苯容易被生物降解,但苯的去除具有一定的难度。  相似文献   

8.
An oil-refining plant site located in southern Taiwan has been identified as a petroleum-hydrocarbon [mainly methyl tert-butyl ether (MTBE) and benzene, toluene, ethylbenzene, and xylenes (BTEX)] spill site. In this study, groundwater samples collected from the site were analyzed to assess the occurrence of intrinsic MTBE biodegradation. Microcosm experiments were conducted to evaluate the feasibility of biodegrading MTBE by indigenous microorganisms under aerobic, cometabolic, iron reducing, and methanogenic conditions. Results from the field investigation and microbial enumeration indicate that the intrinsic biodegradation of MTBE and BTEX is occurring and causing the decrease in MTBE and BTEX concentrations. Microcosm results show that the indigenous microorganisms were able to biodegrade MTBE under aerobic conditions using MTBE as the sole primary substrate. The detected biodegradation byproduct, tri-butyl alcohol (TBA), can also be biodegraded by the indigenous microorganisms. In addition, microcosms with site groundwater as the medium solution show higher MTBE biodegradation rate. This indicates that the site groundwater might contain some trace minerals or organics, which could enhance the MTBE biodegradation. Results show that the addition of BTEX at low levels could also enhance the MTBE removal. No MTBE removal was detected in iron reducing and methanogenic microcosms. This might be due to the effects of low dissolved oxygen (approximately 0.3 mg/L) within the plume. The low iron reducers and methanogens (<1.8×103 cell/g of soil) observed in the aquifer also indicate that the iron reduction and methanogenesis are not the dominant biodegradation patterns in the contaminant plume. Results from the microcosm study reveal that preliminary laboratory study is required to determine the appropriate substrates and oxidation-reduction conditions to enhance the biodegradation of MTBE. Results suggest that in situ or on-site aerobic bioremediation using indigenous microorganisms would be a feasible technology to clean up this MTBE-contaminated site.  相似文献   

9.
Selection of effective groundwater remediation scenarios is a complex issue that requires understanding of contaminants’ transport processes. The effectiveness of cleanup measures may be verified by fate and transport numerical modeling. The goal of this work was to present the usefulness of fate and transport modeling for planning, verification and fulfillment of effective groundwater remediation methods. Selection methodology was developed, which is based on results of numerical flow and transport modeling. A field site located in south-east Poland was selected as a case study, in which groundwater contamination of trichloroethene and tetrachloroethene was detected. The results indicated that “pump and treat” was the most effective among the studied remediation methods, followed by permeable reactive barrier and in situ chemical oxidation. Natural attenuation-based remediation was demonstrated to be the least suitable, as it requires the longest time to reach predefined remediation goals, principally due to low sorption capacity and unfavorable hydrogeochemical conditions for biodegradation. Fate and transport numerical modeling allowed simulating different remediation strategies, and thus the decision-making process was facilitated.  相似文献   

10.
近年来,应用于修复石油烃污染地下水的监测自然衰减技术得到了广泛深入研究,同时质量通量方法已逐渐成为评 估地下水燃油污染场地自然衰减监测修复效能的重要手段。通过在室内砂槽中添加乙醇汽油组分,监测其自然衰减,利用 质量通量方法,得出了BTEX和乙醇的质量减少率、自然衰减速率常数K;结合非反应示踪剂溴离子,评价了BTEX和乙醇 自然衰减因素中吸附和微生物的联合降解效应。结果表明,自然衰减是地下水中燃油组分修复的重要机制,质量通量方法 是评估自然衰减的有效方法之一。BTEX和乙醇在自然衰减过程中被去除的比例分别为78.88%和98.71%,其中约98%的 BTEX 因吸附和生物降解联合作用被去除,接近100%的乙醇因内在生物降解作用被去除;BTEX 的自然衰减速率为 0.077d-1~0.167d-1,乙醇为0.353d-1,自然条件下乙醇比BTEX更容易衰减。  相似文献   

11.
为研究无机水化学离子在降雨径流示踪中的可能性,在实验流域实测降雨、地面径流、壤中流、地下水径流过程和流域内17个测孔的地下水过程中,施测了Na+,K+,Ca2+,Mg2+,Cl-,SO42-,HCO3-+CO32-,NO3-,F-,NH4-,PO42-,SiO2和pH,EC,18O的同步过程,还施测了少数土壤水水样。结果是:①在Ca2+与Cl-/SO42-和EC与Na+/(Na++Ca2+)的关系中以及除NO3-,NH4-,PO42-外的所有离子,都可识别出上述各种径流组分;②径流离子过程均与降雨离子过程相仿,随径流组分从地面到地下而渐趋坦化;③除个例外,离子浓度过程均以降雨为最小并从地面径流到地下水径流渐次增大;④降雨和地下水离子过程表现为径流离子过程的两端元;⑤在降雨和各径流组分中,18O过程与大部分离子过程有一定的同步性。从以上结果认为,降雨并不是流域径流离子输出的主要来源,然而却是形成它的主要控制因素。此外,有关试验结果还对应用Cl-进行地下水补给的估算方法提出了问题。  相似文献   

12.
Polychlorinated biphenyls (PCBs) are the main constituents of clophen (the liquid of the electric transformers and capacitors) and have been characterized as potential human carcinogens. PCBs can be a hazardous contaminant of soil and groundwater. We used the mathematical model variably saturated 2D flow and transport (VS2DT model) to simulate the transport of PCBs from the soil surface to groundwater for a time period of 30 years. We also used a mathematical model to simulate the colloid-facilitated PCB transport, under saturated flow conditions. The results showed that PCBs dissolved in water cannot be transported to large depths in unsaturated soils, because of their strong sorption onto soil and low solubility in water. For soils with very low or no organic matter content, PCB transport is much faster and the probability of groundwater contamination is much higher. PCBs can partition to colloids originating from dissolved organic matter in groundwater. Colloid-facilitated PCB transport is faster compared to PCB transport in aqueous solution with no colloids present.  相似文献   

13.
This study deals with transport of solutes through a saturated sub-surface rock formation with well-defined horizontal parallel fractures. For this purpose, a simplified conceptual model consisting of a single fracture and its associated rock-matrix is considered in the presence of a fracture-skin in order to study the mobility and mixing of solutes along the fracture. In this paper, a coupled fracture-skin-matrix system is modeled numerically using finite difference method in a pseudo two-dimensional domain with a constant continuous source at fracture inlet. Flow and transport processes are considered parallel to the fracture axis, while the transport processes in fracture-skin as well as in rock-matrix are considered perpendicular to the fracture axis. Having obtained the concentration distribution along the fracture, method of spatial moments is employed to study the mobility and spreading of solutes. Sensitivity analyses have been done to understand the effect of various fracture-skin parameters like porosity, thickness, and diffusion coefficient. Further, the influence of non-linear sorption and radioactive decaying of solutes are carried out for different sorption intensities and decay constants. Results suggest that the presence of fracture-skin significantly influences the mobility and spreading of solutes along the fracture in comparison with a coupled fracture-matrix system without fracture-skin.  相似文献   

14.
. The natural attenuation of a binary mixture of toluene and 1,2,4-trimethylbenzene, which was previously experimentally demonstrated in anaerobic column experiments, was simulated with the newly-developed PHREEQC model to reveal the biogeochemical processes involved. The processes considered in this model include advection, diffusion, sorption, redox reactions (e.g., oxidation of toluene and 1,2,4-trimethylbenzene coupled to the reduction of microbial ferric iron), precipitation of secondary minerals such as siderite and magnetite, and dissolution of hydrous ferric oxides, as well as other thermodynamic equilibrium reactions. The functions of advection and diffusion built into the PHREEQC were conventionally simulated. The sorption was kinetically simulated based on a bicontinuum model, whereas biodegradation was described using a multiple-term Monod model. The processes mentioned above were coupled with a geochemical equilibrium model. The consistency between the experimental and modeling results indicates that the processes defined and the controlling parameters chosen could describe the coupled interactions between transport and biogeochemical reactions for the studied system. The discrepancy between modeling and experimental observations, however, also revealed the limitation of the modeling approach. In general, the model approach, which incorporates simplified mathematical representations of the true physico-chemical dynamics of the sorption and biodegradation processes of toluene and 1,2,4-trimethylbenzene under anaerobic conditions is a very efficient and good predictive tool in management and remediation of contaminant groundwater aquifers.  相似文献   

15.
非平衡-非线性吸附情况下填埋场污染物运移分析   总被引:10,自引:0,他引:10  
栾茂田  张金利  杨庆 《岩土力学》2004,25(12):1855-1861
采用Langmuir等温吸附线方程描述非线性吸附性能, 基于改进的混合元方法,通过数值计算与分析,探讨了非平衡吸附条件下污染物运移过程及其机理。计算结果表明: 当考虑非平衡、非线性吸附性能时, 污染物穿透曲线即浓度的时程变化曲线尖锐而狭窄、峰值点前移, “拖长尾”现象不明显, 由此说明,土颗粒对污染物的非平衡、非线性吸附使得污染物的穿透能力增强, 滞留能力下降。进一步的变动参数比较分析表明:Langmuir等温线方程中的参数B、压实粘土衬里的渗透性及地下水渗流速度对污染物运移过程具有显著的影响。  相似文献   

16.
To estimate the behavior of ethanol-blended dissolved BTEX hydrocarbons in groundwater, a quantitative tracing study instead of qualitative analysis was carried out by using a large sand tank, into which 2-L solution including bromide, ethanol and dissolved BTEX was injected under a controlled hydraulic condition. Mean residence time (MRT), pore volume swept by solute (V p), retardation coefficient (R) and biodegradation rate constant (k) of injected solutes were estimated. Compared with bromide that was used as a conservative tracer, ethanol and BTEX had shorter MRT and smaller V p with the sequence of EtOH < T < E < m/p-X < o-X < B < Br. Biodegradation was confirmed as evidenced by the consumptions of dissolved oxygen (DO), nitrate and sulfate, and the production of acetate. The sequence of k as EtOH > T > E > m/p-X > o-X > B was just opposite to the sequences of MRT and V p. The relationship among above sequences implies that MRT and V p can be used as indicators to assess in situ biodegradability of a solute. Biodegradation of a reactive solute can make its MRT shortened and V p shrunk. In addition, the sorption of ethanol could be neglected (R = 1.0), whereas BTEX compounds were adsorbed (R = 1.04–1.15). It should be noted that biodegradation of a solute can affect the estimation of its retardation coefficient. To our knowledge, this paper provides an available route to quantitatively estimate biodegradability of a solute in groundwater.  相似文献   

17.
Industrially sourced dense non-aqueous phase liquids (DNAPLs) contaminated an alluvial aquifer in France decades ago. The location(s) and nature of the pollution source zone(s) were unknown, and the dissolved concentrations of volatile organic compounds in the monitoring wells varied greatly with time. The aquifer was in hydraulic equilibrium with an artificial canal whose water level was highly variable (up to 5 m). These variations propagated into the aquifer, causing changes in the groundwater flow direction; a transient numerical model of flow and solute transport showed that they correlate with the concentration variations because the changes in the flow direction resulted in the contaminant plume shifting. The transient hydrogeological numerical model was built, taking into account solvent biodegradation with first-order chain, since biodegradation has a significant influence on the pollutant concentration evolution. The model parameterization confirms the position of the source zones among the potential troughs in the bedrock where DNAPLs could have accumulated. The groundwater model was successfully calibrated to reproduce the observed concentration variations over several years and allowed a rapid validation of the hypotheses on the functioning of the polluted system.  相似文献   

18.
The detailed understanding of in situ biodegradation of petroleum hydrocarbons in porous aquifers requires knowledge on biogeochemical gradients, the distribution of individual redox species and microorganisms. The generally limited spatial resolution of conventional monitoring wells, however, hampers appropriate characterization of small-scale gradients and thus localization of the relevant processes. Groundwater sampling across a BTEX plume in a sandy aquifer by means of a novel high-resolution multi-level well (HR-MLW) is presented here. The presence of distinct and steep biogeochemical gradients is demonstrated in the centimeter and decimeter scale, which could not be resolved with a conventional multi-level well. The thin BTEX plume with a vertical extension of only 80 cm exhibited a decline of contaminant concentrations by two orders of magnitude within a few centimeters in the upper and lower fringe zone. The small-scale distribution of sulfate, sulfide and Fe(II) in relation to the contaminants and elevated δ34S and δ18O values of groundwater sulfate strongly indicated sulfate and iron reduction to be the dominant redox processes involved in biodegradation. High microbial activities and biomass especially at the plume fringes and the slope of chemical gradients supported the concept that the latter are regulated by microbial processes and transverse dispersion, i.e. vertical mixing of electron donors and acceptors. Transverse dispersion therefore was suggested to be a driving factor controlling biodegradation in porous aquifers, but not exclusively limiting natural attenuation processes at this site. Broad overlapping zones of electron donors and electron acceptors point towards additional factors limiting anaerobic biodegradation in situ. The identification of small-scale gradients substantially contributed to a better understanding of biodegradation processes and hence is a prerequisite for the development of reliable predictive mathematical models and future remediation strategies.  相似文献   

19.
The Madrid Tertiary Detrital Aquifer is one of the largest and most important aquifers of Spain. This paper assesses the most relevant controls on the natural baseline quality and the dominant chemical processes within the aquifer. The hydrochemistry of the groundwater is variable despite the relative uniformity of the detrital sediments. The natural baseline is expressed as a range of values that are controlled by lithological and hydrological factors; spatial variations of groundwater chemistry are related to changes in rock type, water-rock interaction and the residence time of groundwater. The fundamental chemical processes within the Arkosic aquifer are hydrolysis of silicates, dissolution of carbonates, dissolution of evaporites (only in the vicinity of the transitional facies), ion exchange, neoformation of clays, precipitation of silica as cement, and precipitation of carbonates due to increasing temperature along the downward pathways. Some chemical and physico-chemical parameters like pH, dissolved oxygen, and hardness, and several elements like calcium, sodium, magnesium, silica, and arsenic show an evolutionary trend according to groundwater flow path. A gradual increase in arsenic concentration from recharge areas to discharge areas is observed; it is the main natural water constituent that deteriorates the quality of the fresh Madrid groundwater as a drinking water supply. The occasionally elevated arsenic concentrations originate from natural sources. The concentration and mobility of arsenic seems to be controlled by pH-dependent anion exchange processes resulting from the evolution to Na-HCO3 water.  相似文献   

20.
The application of compound-specific stable isotope analysis (CSIA) was evaluated to characterise a complex groundwater contamination. For this purpose, δ13C and δ2H analysis of benzenes and alkylated derivatives were used to interpret both the impact of different sources on a contaminant plume and the presence of degradation processes. The different contaminant sources could be distinguished based on their combined δ13C–δ2H signature of the benzene, toluene, ethylbenzene and xylenes (BTEX) dissolved in the groundwater. Despite this source differentiation, plume characterisation was not possible due to the complex mixing of the respective contaminant plumes. Furthermore, the original isotope signatures of the sources were not preserved across these plumes. To estimate the level of in situ biodegradation independently from concentration data, the Rayleigh equation was used. Although current literature identifies the application of CSIA as very promising in the frame of characterising organic groundwater pollution, this study has indicated that this approach can be limited with respect to successfully distinguish the different plumes and their relation to the known source zones.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号