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1.
A large number of ground water samples (360) was collected from 60 stations over six consecutive seasons to study the influence of the main sewerage drain on shallow ground water table beneath the municipal area of Cuttack, India. A majority of the samples collected from stations close to the drain exceeded the maximum permissible limits set by the World Health Organization (WHO). Almost all the samples near the drain exceeded the WHO limit for NO3- and Na+. However, the concentrations decreased as the distance from the drain increased. The winter season registered the maximum concentrations of NH4+, NO3-, and SO42- ions whereas the minimum values always coincided with the rainy season. R-mode factor analysis was conducted to find relationships amongst the 16 chemical parameters studied. Fluoride showed a negative correlation with Cl-, Na+, NO3-, SO42-, and PO43-. The concentration of F- may be lower in raw waste water than naturally occurs in the ground water. Therefore, a decrease in the concentration of F- near the drain may be attributed to dilution by contributions of waste water to the ground water. The rest of the parameters were found to be directly related to the distance of collection points to the sewerage. The distribution of nutrients is strongly affected by leaching of waste water into the ground water.  相似文献   

2.
Eloctromigraiion offers a potential tool for remediating ground water contaminated with highly soluble components, such as Na+, Cl, NO3 and SO4−. A field experiment was designed to lest the efficacy of electromigration for preconcontrating dissolved SO42 in ground water associated with a fossil-fuel power plant. Two shallow wells, 25 feel apart (one 25 feel deep, the other 47 feet deep), were constructed in the upper portion of an unconfined alluvial aquifer. The wells were constructed with a double-wall design, with an outer casing of 4-inch PVC and an inner lube of 2-inch FVC; both were fully slotted (0.01 inch). Electrodes were constructed by wrapping the inner lulling with a 100-foot length of rare-earth metal oxide/copper wire. An electrical potential of 10.65 volts DC Was applied, and tests were run for periods of 12, 44, and 216 hours. Results showed large changes in the pH from the initial pH of ground water of about 7.5 to values of approximately 2 and 12 at the anode and cathode, respectively. Despite the fact that the test conditions were far from ideal, dissolved SO42-; was significantly concentrated at the anode. Over a period of approximately nine days, the concentration of SO42- at the anode reached what appeared to he a steady-state value of 2200 mg/L. compared lo the initial value in ground water of approximately 1150 mg/L. The results of this field lest should encourage further investigation of electromigration as a tool in the remediation of contaminated ground water.  相似文献   

3.
Kelly WR 《Ground water》2008,46(5):772-781
The rapid expansion of major cities throughout the world is resulting in the degradation of water quality in local aquifers. Increased use of road deicers since the middle of the 20th century in cities in the northern United States, Canada, and Europe has been linked to degraded ground water quality. In this article, Chicago, Illinois, and its outlying suburban areas are used as an example of the effects of urbanization in a historical context. A statistical study of historical water quality data was undertaken to determine how urbanization activities have affected shallow (<60 m) ground water quality. Chloride (Cl−) concentrations have been increasing, particularly in counties west and south of Chicago. In the majority of shallow public supply wells in the western and southern counties, Cl− concentrations have been increasing since the 1960s. About 43% of the wells in these counties have rate increases greater than 1 mg/L/year, and 15% have increases greater than 4 mg/L/year. Approximately 24% of the samples collected from public supply wells in the Chicago area in the 1990s had Cl− concentrations greater than 100 mg/L (35% in the western and southern counties); median values were less than 10 mg/L before 1960. The greater increase in Cl− concentrations in the outer counties is most likely due to both natural and anthropogenic factors, including the presence of more significant and shallower sand and gravel deposits, less curbing of major highways and streets, and less development in some parts of these counties.  相似文献   

4.
Treatment of nitrogen in landfill leachate has received considerable attention recently because of the relatively low levels at which some nitrogen species (i.e., NH3) can be toxic to aquatic life forms. This study reports on the results of a three-year, pilot-scale field trial demonstrating the use of infiltration bed and nitrate barrier technology to achieve nitrogen removal in landfill leachate. The infiltration bed comprises an unsaturated sand layer overlying a saturated layer of waste cellulose solids (sawdust), which acts as a carbon source for heterotrophic denitrification. When loaded at a rate of 1 to 3 cm/day, the infiltration bed was successful at lowering leachate inorganic nitrogen (NH4++ NO3-) levels averaging 24.8 mg/L N by 89%, including 96% in the third year of operation. The surface water discharge criteria for un-ionized ammonia (NH3) were met on all occasions in the treated leachate during the second and third years of operation. Nitrogen attenuation is presumed to occur by a two-step process in which leachate NH4+ is first oxidized to NO3- in the unsaturated sand layer and then is converted to nitrogen gas (N2) by denitrification occurring in the underlying sawdust layer. Mass balance calculations suggest that the sawdust layer has sufficient carbon to allow denitrification to proceed for long periods (1.0 to 30 years) without replenishment. Because this technology is simple to construct and is relatively maintenance free, it should be attractive for use at smaller landfills where the installation of conventional treatment plants may not be feasible.  相似文献   

5.
A small-scale field experiment was carried out to demonstrate the effectiveness of using septic system -type infiltration beds for on-site treatment of landfill leachate. Using an infiltration bed with a 3-m-thick vadose zone of medium sand, and loaded at a rate 01 18 cm/day, a treatment efficiency of >99 percent was obtained for Fe, 94 percent for NH4+, and 54 percent for dissolved organic carbon (DOC). Attenuation occurred during one- to two-day residency in the aerobic vadose zone (pore gas O2 > 12 percent by volume) as a result of oxidation reactions that caused nitrification of NH4+, convened Fe2+ to Fe3+ allowing subsequent precipitation of sparingly soluble Fe oxyhydroxide minerals, and biodegraded DOC. Attenuation of an aerobically degradable trace volatile organic compound (dichlorobenzene) was also noted, although other less degradable compounds (trichloroethylene and tetrachloroethylene) persisted.
Fe mineral precipitation caused a discontinuous hardpan layer to occur in the zone immediately below the infiltration pipes. However, this layer did not become impermeable or continuous enough to significantly impede infiltration during the 82-day experiment.
Advantages of this technology for leachate treatment are that it is low cost, it is simple to construct and operate. and treatment occurs on-site, avoiding the cost of transporting leachate off-site for treatment.  相似文献   

6.
Water was sampled from eight springs and a lake in volcanic Miyakejima Island of Japan after the 2000 eruption. Major chemical and isotopic compositions of the water were analyzed. Significant increases of sulfate ion are observed in several springs where the thickness of ejecta exceeds 32 mm. A good relationship of Cl/S mole ratios between spring water and leachate of the ejecta is observed. Sulfur isotopic compositions of the spring water become close to that of leachate of the ejecta as time elapses after the eruption. Consequently the sources of the added sulfate ion in the spring water after the eruption are interpreted to be anhydrite and adhered sulfur of the ejecta.  相似文献   

7.
Abstract
Determination of chemical constituent ratios allows distinction between two salinization mechanisms responsible for shallow saline ground water and vegetative-kill areas in parts of west Texas. Mixing of deep-basin (high Cl) salt water and shallow (low Cl) ground water results in saline waters with relatively low Ca/Cl, Mg/Cl, SO44/ Cl, Br/Cl, and NO3/Cl ratios. In scattergrams of major chemical constituents vs. chloride, plots of these waters indicate trends with deep-basin brines as high Cl end members. Evaporation of ground water from a shallow water table, in contrast, results in saline water that has relatively high Ca/Cl, Mg/Cl, SO4/Cl, and Br/CL ratios. Trends indicated by plots of this water type do not coincide with trends indicated by plots of sampled brines. Leaching of soil nitrate in areas with a shallow water table accounts for high NO3 concentrations in shallow ground water.  相似文献   

8.
A six year field experiment has shown that a sand-bentonite mixture used to seal monitoring wells in aquitards contributes solutes to the ground water sampled from these wells. Monitoring wells were installed at field sites with hydraulic conductivity (K) ranging from 5 × 10 -9 m/s to 3 × 1011 m/s. In most cases the boreholes remained dry during installation which allowed the placement of a dry powdered bentonite/sand mixture tagged with potassium bromide (KBr) to seal and separate sampling points. Over six years, wells were sampled periodically and ground-water samples were analyzed for Br and Cl and other major ions. Typical Br results ranged from 10 mg/1 to 35 mg/1 in the first 700 days, as compared to an estimated initial concentration in the seal material of about 75 mg/1. After six years the bromide concentrations had decreased to between 3 mg/1 and 5 mg/1. The total mass of Br removed in six years is less than 50% of that placed; therefore the contamination effects, although considerably diminished, persist. The trends of Br, Cl, Na, and SO4 indicate that varying degrees of contamination occur. These data show that the materials used to seal monitoring wells in aquitards can have a significant and long-lasting impact on the chemistry of the water in the wells.  相似文献   

9.
Electromigration is proposed as an in situ method for preconcentrating contaminants in ground water prior to pumping and treating. In earlier investigations by the senior author and co-workers, it was found that Cu in synthetic ground water migrated strongly to a Pt cathode and plated out as metallic copper. In the present study, carbon electrodes were inserted into a laboratory column of fine quartz sand that was saturated with a lower concentration of CuSO4 solution. A fixed potential of 2.5 V was applied, causing dissolved Cu and SO4 to accumulate strongly at the cathode and anode, respectively. Only minor plating-out of Cu took place on the carbon electrodes. In addition to the use of carbon electrodes, the present research also investigated the effects of a lower concentration of metal, accumulation of SO4 adjacent to the anodes, adsorption of Cu on the sand, and competition by moving ground water.
At an imposed voltage of 2.5 V and in the presence of 65 mg/L of dissolved Cu and 96 mg/L of SO4 (0.001 M CuSO4 solution), electrolysis of water caused large changes in the pH and speciation of the aqueous components, as well as precipitation of solid Cu-hydroxides. Significant retardation of Cu occurred in the presence of ground water flowing at an average intergranular velocity of 0.2 m/day, but only minor retardation at water velocities of 1.9 and 2.9 m/day.
Sulfate tends to migrate strongly to the anodes, suggesting that in situ electromigration may offer a useful new method for preconcentrating such highly soluble ions as SO4, NO3, and CI that are difficult to remove by conventional pump-and-treat methods. A number of potential problems exist that should be addressed in a field test.  相似文献   

10.
Installation of a permeable reactive barrier to intercept a phosphate (PO4) plume where it discharges to a pond provided an opportunity to develop and test methods for monitoring the barrier's performance in the shallow pond-bottom sediments. The barrier is composed of zero-valent-iron mixed with the native sediments to a 0.6-m depth over a 1100-m2 area. Permanent suction, diffusion, and seepage samplers were installed to monitor PO4 and other chemical species along vertical transects through the barrier and horizontal transects below and near the top of the barrier. Analysis of pore water sampled at about 3-cm vertical intervals by using multilevel diffusion and suction samplers indicated steep decreases in PO4 concentrations in ground water flowing upward through the barrier. Samples from vertically aligned pairs of horizontal multiport suction samplers also indicated substantial decreases in PO4 concentrations and lateral shifts in the plume's discharge area as a result of varying pond stage. Measurements from Lee-style seepage meters indicated substantially decreased PO4 concentrations in discharging ground water in the treated area; temporal trends in water flux were related to pond stage. The advantages and limitations of each sampling device are described. Preliminary analysis of the first 2 years of data indicates that the barrier reduced PO4 flux by as much as 95%.  相似文献   

11.
The area surrounding the Colorado Department of Transportation Materials Testing Laboratory in Denver was the subject of intense investigation, involving the collection of thousands of ground water, soil-gas, and indoor air samples in order to investigate indoor air impacts associated with a subsurface release of chlorinated solvents. The preremediation portion of that data set is analyzed and reduced in this work to ground water–to-indoor air attenuation factors (αgw= the ratio of the measured indoor air concentration to the soil-gas concentration predicted to be in equilibrium with the local ground water concentration). The empirical αgw values for this site range from about 10−6 to 10−4 with an overall average of 3 × 10−5 (μg/L indoor air)/(μg/L soil gas). The analysis of this data set highlights the need for a thorough data review and data screening when using large data sets to derive empirical relationships between subsurface concentrations and indoor air. More specifically, it is necessary to identify those parts of the data that contain a strong vapor intrusion pathway signal, which generally will require concentrations well above reported detection levels combined with spatial or temporal correlation of subsurface and indoor concentrations.  相似文献   

12.
Geographical distribution of helium isotope ratios in northeastern Japan   总被引：1，自引：0，他引：1  
Keika  Horiguchi  Sadato  Ueki  Yuji  Sano  Naoto  Takahata  Akira  Hasegawa  George  Igarashi 《Island Arc》2010,19(1):60-70
In order to study the precise geographical distribution of helium isotope ratios in northeastern Japan and compare it with geophysical data, we collected 43 gas and water samples from hot and mineral springs in the region where the ratio had never been reported, and measured the 3He/4He and 4He/20Ne ratios of these samples. It was found that the 3He/4He ratios show clear contrasts between the forearc and the back-arc regions in the Tohoku district in northeastern Japan. In the forearc region, the ratios are smaller than 1 RA (1 RA = 1.4 × 10−6; RA means the 3He/4He ratio of the atmosphere). On the other hand, those along the volcanic front and in the back-arc region are apparently higher. Moreover, we found a variation in the 3He/4He ratios along the volcanic front. In Miyagi Prefecture (38–39°N), the ratios range from 2 to 5 RA. On the other hand, the ratios are less than 1 RA in and around the southern border between Iwate and Akita Prefectures (39–39.5°N). Comparing the distribution of helium isotope ratios to results of recent geophysical studies, we found that the features in geographical distribution of helium isotope ratios are similar to those of seismic low-velocity zone distributions and high Qp−1 distributions in the uppermost mantle. These observations strongly suggest that the helium isotope ratios reflect the distribution of melts in the uppermost mantle and are a useful tool for investigating the origin, behavior, and distribution of deep fluids and melts.  相似文献   

13.
Abstract Elemental and isotopic compositions of noble gases extracted from the bore hole water in Osaka plain, central Japan were examined. The water samples were collected from four shallow bore holes (180-450 m) and seven deep bore holes (600-1370 m) which have been used for an urban resort hot spring zone. The water temperatures of the deep bore holes were 22-50°C and that of the shallow bore holes, 13-23°C. The elemental abundance patterns show the progressive enrichment of the heavier noble gases compared with the atmospheric noble gas composition except for He, which is heavily enriched in deep bore hole water samples. 3He/4He ratios from the bore holes reaching the Ryoke granitic basement were higher than the atmospheric value (1.4 × 10−6), indicating a release of mantle He through the basement. The highest value of 8.2 × 10−6 is in the range of arc volcanism. On the other hand, the bore holes in sedimentary rocks overlying the basement release He enriched in radiogenic 4He, resulted in a low 3He/4He ratio of 0.5 × 10−6. 4He/20Ne and 40Ar/36Ar ratios indicate that the air contamination is generally larger in shallow bore holes than in deep ones from each site. The helium enriched in mantle He is compatible with the previous work which suggested up-rising magma in 'Kinki Spot', the area of Osaka and western Wakayama, in spite of no volcanic activity in the area. A model to explain an initiation of magma generation beneath this area is presented.  相似文献   

14.
A conceptual model of eolian transport is proposed to address the widely distributed, high concentrations of hexavalent chromium (Cr+6) observed in ground water in the Emirate of Abu Dhabi, United Arab Emirates. Concentrations (30 to more than 1000 μg/L Cr+6) extend over thousands of square kilometers of ground water systems. It is hypothesized that the Cr is derived from weathering of chromium-rich pyroxenes and olivines present in ophiolite sequence of the adjacent Oman (Hajar) Mountains. Cr+3 in the minerals is oxidized to Cr+6 by reduction of manganese and is subsequently sorbed on iron and manganese oxide coatings of particles. When the surfaces of these particles are abraded in this arid environment, they release fine, micrometer-sized, coated particles that are easily transported over large distances by wind and subsequently deposited on the surface. During ground water recharge events, the readily soluble Cr+6 is mobilized by rain water and transported by advective flow into the underlying aquifer. Chromium analyses of ground water, rain, dust, and surface (soil) deposits are consistent with this model, as are electron probe analyses of clasts derived from the eroding Oman ophiolite sequence. Ground water recharge flux is proposed to exercise some control over Cr+6 concentration in the aquifer.  相似文献   

15.
Non-point source pollution of ground water systems has become a national concern in recent years. Researchers and regulatory agencies are investigating the source and processes of the contamination. Agricultural best management practices (BMPs) traditionally developed to reduce non-point source pollution of surface water resources are being investigated for their impact on ground water quality. This study used the CREAMS model to simulate the long-term effects of seven different BMPs on nitrate nitrogen (NO3-N) loadings to a shallow, unconfined ground water system. Two representative watersheds, 5.8 and 8.9 hectares (14.3 and 22 acres) in area, in the Coastal Plain physiographic region of Maryland were selected for study. Soils in these watersheds belong to the Matapeake silt loam series and have moderate infiltration capacity. Results from this study indicated that BMPs used in conjunction with winter cover (barley) reduced NO3-N leaching to the ground water system. It was also found that turfgrass reduced surface losses of water and nitrogen, but increased leaching losses of water and NO3-N significantly. All of the BMPs simulated in this study resulted in leachate NO3-N concentrations exceeding 10 ppm, the U.S. EPA health standard for public drinking water, indicating a need for alternate practices for reducing nitrate leaching.  相似文献   

16.
Soil-solution samplers and shallow ground water monitoring wells were utilized to monitor nitrate movement to ground water following H2O2 application to a clogged soil absorption system. Nitrate-nitrogen concentrations in soil water and shallow ground water ranged from 29 to 67 mg/L and 9 to 22 mg/L, respectively, prior to H2O2 treatment. Mean nitrate-nitrogen concentrations in soil water and ground water increased and ranged from 67 to 115 mg/L and 23 to 37 mg/L, respectively, one week after H2O2 application. Elevated concentrations of nitrate-nitrogen above background persisted for several weeks following H2O2 treatment. The H2O2 treatment was unsuccessful in restoring the infiltrative capacity of a well-structured soil. Application of H2O2 to the soil absorption system poses a threat of nitrate contamination of ground water and its usefulness should be fully evaluated before rehabilitation is attempted.  相似文献   

17.
A 5-year-old wood particle reactor treating agricultural tile drainage in southern Ontario was monitored for its ongoing ability to treat both nitrate (NO3–) and perchlorate (ClO4–). Prior to sampling undertaken in the fifth year of operation, a highway safety flare containing ClO4– was immersed in the inlet pipe elevating influent ClO4– concentrations to up to 33.7 μg/L. ClO4– removal rates were inhibited in the presence of more than 1 to 2 mg/L NO3–-N, but increased rapidly to about 60 μg/L/d upon NO3– depletion. Nitrate removal rates, measured subsequently in the sixth and seventh years of operation, varied with temperature in the range of 2 to 16 mg N/L/d, but remained similar to rates measured in the second year. Additionally, no deterioration in the hydraulic conductivity (K) of the coarse core layer (0.5 3– removal rates and can remain highly permeable over a number of years. The media can also provide high removal rates for other redox sensitive contaminants such as ClO4–. The ability to directly measure the reactor flow rate, in this case via an outlet pipe, greatly simplified the task of estimating hydraulic properties and reaction rates.  相似文献   

18.
Studies have shown that materials, such us polytetra-fluoroethylene (PTFE), rigid polyvinyl chloride (rigid PVC). flexible polyvinyl chloride (flexible PVC), stainless steel (SS). low-density polyethylene (LDPE), and high-density polyethylene (HDPE), have the potential to influence certain analyte concentrations in ground water samples. The effects of HDPE, LDPE, PTFE, rigid PVC, and SS on aqueous concentrations of nitrate-N, atrazine, deethylatrazine (DEA), and deisopropylatrazine (DIA) were evaluated in a field study A laboratory study was conducted to evaluate sorption of atrazine DEA, DIA, cyanazine, alachlor, metolachlor, and butachlor to PTFE, HDPE, and SS materials. Butachlor is rarely use in the United States, but was included because of its expected high sorptivity. No significant differences between HDPE, LDPE, PTFE, rigid PVC, and SS were determined for any of the analytes tested in the field study. In the laboratory study, sorption of DIA to PTFE and SS was significant at 2.6 × 10−5 and 4.1 × 10−5μg/m2 respectively. Sorption of DIAA to HDPE was not significantly > 0 sorption of all other compounds to HDPE, PTFE, and SS were also not significantly >0. Results of the two studies indicate that for these analytes (relatively polar or ionized compounds), representative ground water samples are not dependent on the materials used for multilevel sampler construction. When considering these compounds, it appears that the least expensive materials (HDPE, rigid PVC, and LDPE) are good choices for the construction of ground water monitoring wells.  相似文献   

19.
Sharma S  Frost CD 《Ground water》2008,46(2):329-334
Recovery of hydrocarbons commonly is associated with coproduction of water. This water may be put to beneficial use or may be reinjected into subsurface aquifers. In either case, it would be helpful to establish a fingerprint for that coproduced water so that it may be tracked following discharge on the surface or reintroduction to geologic reservoirs. This study explores the potential of using δ13C of dissolved inorganic carbon (DIC) of coalbed natural gas (CBNG)–coproduced water as a fingerprint of its origin and to trace its fate once it is disposed on the surface. Our initial results for water samples coproduced with CBNG from the Powder River Basin show that this water has strongly positive δ13CDIC (12‰ to 22‰) that is readily distinguished from the negative δ13C of most surface and ground water (−8‰ to −11‰). Furthermore, the DIC concentrations in coproduced water samples are also high (more than 100 mg C/L) compared to the 20 to 50 mg C/L in ambient surface and ground water of the region. The distinctively high δ13C and DIC concentrations allow us to identify surface and ground water that have incorporated CBNG-coproduced water. Accordingly, we suggest that the δ13CDIC and DIC concentrations of water can be used for long-term monitoring of infiltration of CBNG-coproduced water into ground water and streams. Our results also show that the δ13CDIC of CBNG-coproduced water from two different coal zones are distinct leading to the possibility of using δ13CDIC to distinguish water produced from different coal zones.  相似文献   

20.
Tomohiro  Toki  Toshitaka  Gamo  Urumu  Tsunogai 《Island Arc》2006,15(3):285-291
Abstract   We collected free-gas and in situ fluid samples up to a depth of 200.6 m from the Sagara oil field, central Japan (34°44'N, 138°15'E), during the Sagara Drilling Program (SDP) and measured the concentrations and stable carbon isotopic compositions of CH4 and C2H6 in the samples. A combination of the CH4/C2H6 ratios with the carbon isotope ratios of methane indicates that the hydrocarbon gases are predominantly of thermogenic origin at all depths. The isotope signature of hydrocarbon gases of δ13      < δ13     suggests that these gases in the Sagara oil field are not generated by polymerization, but by the decomposition of organic materials.  相似文献   

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