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1.
《Ground Water Monitoring & Remediation》2000,20(1):56-68
In these studies, the efficiency of various decontamination protocols was tested on small pieces of materials commonly used in ground water sampling devices. Three materials, which ranged in ability to sorb organic solutes, were tested: stainless steel (SS), rigid polyvinyl chloride (PVC), and polytetrafluoroethylene (PTFE). The test pieces were exposed to two aqueous test solutions: One contained three volatile organic compounds (VOCs) and one nitroaromatic compound, and the other contained four pesticides. Also, three types of polymeric tubing were exposed to pesticide solutions. Generally, the contact times were 10 minutes and 24 hours for sorption and desorption.
The contaminants were removed from the nonpermeable SS and the less-sorptive rigid PVC test pieces simply by washing with a hot detergent solution and rinsing with hot water. Additional treatment was required for the PTFE test pieces exposed to the VOCs and for the low-density polyethylene (LDPE) tubing exposed to the pesticide test solution. Solvent rinsing did not improve removal of the three VOCs from the PTFE and only marginally improved removal of the residual pesticides from the LDPE. However, a hot water and detergent wash and rinse followed by oven drying at approximately 105°C was effective for removing the VOCs from the PTFE and substantially reduced pesticide contamination from the LDPE. 相似文献
The contaminants were removed from the nonpermeable SS and the less-sorptive rigid PVC test pieces simply by washing with a hot detergent solution and rinsing with hot water. Additional treatment was required for the PTFE test pieces exposed to the VOCs and for the low-density polyethylene (LDPE) tubing exposed to the pesticide test solution. Solvent rinsing did not improve removal of the three VOCs from the PTFE and only marginally improved removal of the residual pesticides from the LDPE. However, a hot water and detergent wash and rinse followed by oven drying at approximately 105°C was effective for removing the VOCs from the PTFE and substantially reduced pesticide contamination from the LDPE. 相似文献
2.
Alan D. Hewitt 《Ground Water Monitoring & Remediation》1992,12(2):131-136
Static leaching and sorption laboratory studies were performed to assess the potential of polyvinyl chloride (PVC), polytetrafluoroethylene (PTFE), and two types of stainless steel (SS 304 and SS 316) well casing materials to influence metal concentrations in ground water solutions with low dissolved oxygen. Overall, PTFE was inert, whereas one or both stainless steels significantly altered the solution concentrations of Cd, Cr, Cu, Pb, Fe, and Ni. PVC was generally more reactive than PTFE, but did not significantly alter the solution metal concentrations as often, or as greatly, as either of the stainless casings. 相似文献
3.
Louise V. Parker Alan D. Hewitt Thomas F. Jenkins 《Ground Water Monitoring & Remediation》1990,10(2):146-156
Four well casing materials — polyvinyl chloride (PVC), polytetrafluoroethylene (PTFE), and stainless steel 304 (SS 304) and 316 (SS 316) — were examined to determine their suitability for monitoring inorganic and organic constituents in well water.
The inorganic study used a factorial design to test the effect of concentration of mixed metals (arsenic [As], chromium [Cr], lead [Pb], and cadmium [Cd]), pH, and organic carbon. Sample times were 0.5, 4, 8, 24, and 72 hours. Except for slow loss of Pb, PTFE well casings had no significant effect on the concentration of metals in solution. For the other casings, changes in analyte concentration often exceeded 10 percent in eight hours or less and, thus, could bias analyses of samples taken from wells constructed with these materials. Specifically, PVC casings sorbed Pb and leached Cd; SS 316 casings sorbed As and Pb and leached Cd; and SS 304 casings sorbed As, Cr, and Pb and leached Cd. Both stainless steel casing materials showed markedly poorer performance than the PVC casings.
The well casings were also tested for sorption/desorption of 10 organic substances from the following classes: chlorinated alkehes, chlorinated aromatics, nitroaromatics and nitramines. Sample times were 0, 1, 8, 24, and 72 hours, seven days, and six weeks. There were no detectable losses of analytes in any of the sample solutions containing stainless steel well casings. Significant loss of some analytes was observed in sample solutions containing plastic casings, although losses were always more rapid with the PTFE casings than with PVC. Chlorinated organic substances were lost most rapidly. For samples containing PTFE casings, losses of some of these compounds were rapid enough (>10 percent in eight hours) to be of concern for ground water monitoring. Losses of hydrophobic organic constituents in samples containing PTFE casings were correlated with the compound's octanol/water partition coefficient. 相似文献
The inorganic study used a factorial design to test the effect of concentration of mixed metals (arsenic [As], chromium [Cr], lead [Pb], and cadmium [Cd]), pH, and organic carbon. Sample times were 0.5, 4, 8, 24, and 72 hours. Except for slow loss of Pb, PTFE well casings had no significant effect on the concentration of metals in solution. For the other casings, changes in analyte concentration often exceeded 10 percent in eight hours or less and, thus, could bias analyses of samples taken from wells constructed with these materials. Specifically, PVC casings sorbed Pb and leached Cd; SS 316 casings sorbed As and Pb and leached Cd; and SS 304 casings sorbed As, Cr, and Pb and leached Cd. Both stainless steel casing materials showed markedly poorer performance than the PVC casings.
The well casings were also tested for sorption/desorption of 10 organic substances from the following classes: chlorinated alkehes, chlorinated aromatics, nitroaromatics and nitramines. Sample times were 0, 1, 8, 24, and 72 hours, seven days, and six weeks. There were no detectable losses of analytes in any of the sample solutions containing stainless steel well casings. Significant loss of some analytes was observed in sample solutions containing plastic casings, although losses were always more rapid with the PTFE casings than with PVC. Chlorinated organic substances were lost most rapidly. For samples containing PTFE casings, losses of some of these compounds were rapid enough (>10 percent in eight hours) to be of concern for ground water monitoring. Losses of hydrophobic organic constituents in samples containing PTFE casings were correlated with the compound's octanol/water partition coefficient. 相似文献
4.
This report examines sorption of low ppb levels of organic solutions by polytetra- fluoroethylene (PTFE), rigid polyvinyl chloride (PVC), and stainless steel 304 and 316 well casings. Nineteen organics were selected, including several munitions and chlorinated solvents. Compounds were selected to offer a range of physical properties, such as solubility in water, octanol/water partition coefficient, and molecular structure. When these results were compared with the results from a similar study conducted at ppm levels, the rate and extent of sorption by PTFE and PVC were the same as seen previously for almost all analytes. There were no losses of any compounds associated with stainless steel. At these low levels (ppm and ppb), the rate of diffusion within the polymer (PVC and PTFE) is independent of concentration. Only with PTFE are the rates rapid enough to be of concern when monitoring for some contaminants in ground water. Tetrachloroethylene was the compound PTFE sorbed the most rapidly. The study showed that PVC well casings are suitable for monitoring low levels (ppm and ppb) of organics. 相似文献
5.
This series of experiments was initiated to determine the overall suitability of three alternative polymeric well casing materials (fluorinated ethylene propylene [FEP], fiberglass-reinforced epoxy [FRE], and fiberglass-reinforced plastic [FRP]) for use in ground water monitoring wells and to compare these materials with polyvinyl chloride (PVC) and polytetrafluoroethylene (PTFE) well casings. This paper focuses on sorption and leaching of metals.
Generally, the fiberglass materials leached more metal contaminants than PVC, FEP, and PTFE. However, with one exception (Pb leaching from FRP), leached concentrations were below maximum allowable limits set by the U.S. Environmental Protection Agency (EPA) for drinking water. With respect to sorption, none of the polymers sorbed the anions tested, but all of them sorbed one or more of the cations tested. FEP and PTFE were much less sorptive than the other materials. 相似文献
Generally, the fiberglass materials leached more metal contaminants than PVC, FEP, and PTFE. However, with one exception (Pb leaching from FRP), leached concentrations were below maximum allowable limits set by the U.S. Environmental Protection Agency (EPA) for drinking water. With respect to sorption, none of the polymers sorbed the anions tested, but all of them sorbed one or more of the cations tested. FEP and PTFE were much less sorptive than the other materials. 相似文献
6.
Electrokinetic phenomena associated with a water injection experiment at the Nojima fault on Awaji Island, Japan 总被引：2，自引：0，他引：2
Hideki Murakami Takeshi Hashimoto Naoto Oshiman Satoru Yamaguchi Yoshimori Honkura Norihiko Sumitomo 《Island Arc》2001,10(3-4):244-251
Abstract Self-potential variations were measured to estimate the magnitude of electrokinetic and hydrological parameters (zeta potential and permeability) of the Nojima Fault zone in Awaji, Japan. The study observed self-potential variations that seemed to be associated with water flow from the injection well to the fracture zone, which were induced by turning the injection on and off. Amplitudes of the variations were a few to 0.03 V across 320–450 m dipoles. These variations can be explained well with an electrokinetic model. The quantity k/ζ (permeability/zeta potential) is in the range 1.6 × 10−13 − 5.4 × 10−13 m2 /V. Permeability of the Nojima fault zone can be estimated as approximately 10−16 –10−15 m2 on the assumption that the zeta potential is in the range –0.01 to –0.001 V. 相似文献
7.
P.C. Johnson R.A. Ettinger J.P. Kurtz R. Bryan J.E. Kester 《Ground Water Monitoring & Remediation》2009,29(1):153-159
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
8.
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. 3 He/4 He 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 4 He, resulted in a low 3 He/4 He ratio of 0.5 × 10−6 . 4 He/20 Ne and 40 Ar/36 Ar 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
9.
Previous research has shown that the most commonly used well casing materials-stainless steel. polyvinyl chloride (PVC). and polytetra-fluoroethylene (PTFE)-are not suited for all monitoring environments and applications. This study is part of a series of experiments that were conducted to determine the suitability of four other polymeric well casing materials-acrylonitrile butadiene styrene (ABS), fluorinalcd ethylene propylene (FHP), fiberglass-reinlorced epoxy (FRE), and fiberglass-reinforced plastic (FRP)- for use in ground water monitoring wells. In these studies, these four materials were compared with two other commonly used polymeric well casings, PVC and PTFE. Part I of these studies examines the resistance of these materials to degradation by chemicals. Future reports will consider sorption and leaching of organic and metal contaminants.
In this study, the six materials were exposed to 28 neat organic compounds (including one acid) and to extremely acidic and alkaline aqueous solutions for up to 112 days. This was done to simulate the most aggressive environments to which monitoring well casings may be exposed. The casings were observed for changes in weight and signs of physical degradation (swelling, softening, deterioration, or dissolution).
The two fluorinated polymers (FEP and PTFE) were not degraded by any of the lest chemicals. Among the nonfluorinated products tested. FRE was the most inert. Three organic chemicals caused the glass fibers to separate. and two organic solvents caused weight gains exceeding 10 percent. ABS was the most readily degraded material tested. By the end of the study, only the acid and alkaline solutions had little effect on ABS. FRP was more severely degraded by the organic chemicals than FRH but was less affected than PVC. FRP and FRE. lost weight when exposed to the highly acidic conditions. 相似文献
In this study, the six materials were exposed to 28 neat organic compounds (including one acid) and to extremely acidic and alkaline aqueous solutions for up to 112 days. This was done to simulate the most aggressive environments to which monitoring well casings may be exposed. The casings were observed for changes in weight and signs of physical degradation (swelling, softening, deterioration, or dissolution).
The two fluorinated polymers (FEP and PTFE) were not degraded by any of the lest chemicals. Among the nonfluorinated products tested. FRE was the most inert. Three organic chemicals caused the glass fibers to separate. and two organic solvents caused weight gains exceeding 10 percent. ABS was the most readily degraded material tested. By the end of the study, only the acid and alkaline solutions had little effect on ABS. FRP was more severely degraded by the organic chemicals than FRH but was less affected than PVC. FRP and FRE. lost weight when exposed to the highly acidic conditions. 相似文献
10.
Abstract A loam section near Daisen volcano, South-west Japan, has been examined for low-field magnetic susceptibility (MS) and fine quartz accumulation rate. Fission track dating of tephra layers interbedded in the deposit shows that the loam age ranges from about 200 ka to the Present. The MS was measured for both bulk sample and the < 63 μm fine fraction. Fine quartz contents in the < 63 μm fraction were also determined using acid-alkali digestions and recalculated to derive fine quartz accumulation rate (Rqz). Grain size analysis was then carried out on the separated fine quartz. Low-field MS varies from low frequency magnetic suspectibility (χ(LF)) 5 to 100 (× 10−6 m3 /kg) for bulk samples and from 1 to 30 for fine fractions. The fine fraction χ(LF) variation correlated with Chinese loess MS stratigraphy, which indicated changes in pedogenic enhancement of the MS and is reflected by summer monsoon intensity. The Rqz are high in cool climate stages, with volumes between 0.2 and 0.4 (× 10−2 kg/m2 per yr), whereas in warm stages the rate falls to about 0.1. These values compare well with those reported from the Hokkaido and Kanto areas, suggesting the fine quartz originates from tropospheric dust. The strong winter monsoons during glacial stages alternated with weak summer monsoons as a result of a southward shift of the jet stream. In interglacials, summer monsoons were stronger. Seasonal alternating monsoons appear to have operated in South-west Japan through the past 200 000 years. 相似文献
11.
Aerobic biodegradation can be enhanced within contaminant plumes by elevating typically low dissolved oxygen (D.O.) levels using materials or devices that passively release oxygen. We have developed passive devices that provide a uniform, steady, long-term source of oxygen by diffusion from pressurized polymeric tubing and report test results under lab and field conditions. Lab flow-through reactor tests were conducted to determine the diffusion coefficient (D) of oxygen through four readily available tubing materials. Oxygen diffusion was greatest through Tygon® 3350 platinum-cured silicone (D = 6.67 ± 10-7 cm2 /sec), followed by 2075 Ultra Chemical Resistant Tygon (1.59 ± 10-7 cm2 /sec), 2275 High Purity Tygon (5.11 ± 10-8 cm2 /sec), and low-density polyethylene (LDPE; 1.73 ± 10-8 cm2 /sec). Variable-pressure release tests with LDPE resulted in very close estimates of D, which confirmed that mass transfer is controlled by diffusion and that the concentration gradient is a valid approximation of the chemical potential driving diffusion. LDPE emitter devices were designed and installed in seven 8-inch-diameter well screens across a portion of a gasoline plume at a former service station. With the devices pressurized to 620.5 kPag (kilopascals gauge) late in the test, steady-state D.O. concentrations reached as high as 25 mg/L, comparing favorably to the value predicted using the mass-transfer coefficient estimated from the lab test (26.3 mg/L). The method can also be used to release other gases for other reasons: gaseous tracers (i.e., sulphur hexafluoride, helium, and argon), hydrogen (for reductive dechlorination), or light alkanes (for cometabolic biodegradation of methyl tertiary butyl ether [MTBE] or chlorinated solvents). 相似文献
12.
This paper contains the results of a laboratory study that was designed to compare sorption of low (mg/L) concentrations of 11 organic solutes by six polymeric materials (acrylonitrile butadiene styrene [ABS], fluorinated ethylene propylene [FEP], fiberglass-reinforced epoxy [FRE] and fiberglass-reinforced plastic [FRP], polyvinyl chloride [PVC], and poly-tetrafluoroethylene [PTFE]).
During this six-week study, ABS sorbed analytes much more rapidly and to a greater extent than did the other materials, and PVC and FRE sorbed analytes more slowly and to a lesser extent than the other materials tested.
As the study progressed, an increasing number of spurious peaks were found in the high performance liquid chromatography (HPLC) chromatograms of some of our samples, indicating that leaching of some consituents had occurred. By the end of the study, there were 11 additional peaks in the ABS samples, five in the FRP samples, and one in the FRE samples. Analysis by purge and trap gas chromatography/mass spectrometry (GC/MS) of those samples and of well water samples that were exposed to the casings for 500 hours revealed the identity of some of the leached constituents; acrylonitrile and styrene (components of ABS), chloroform and ethylbenzene (an intermediate in the production of styrene) from the ABS pipe, and toluene, 1,1,1-trichloroethane, and ethylbenzene from the FRP casing. 相似文献
During this six-week study, ABS sorbed analytes much more rapidly and to a greater extent than did the other materials, and PVC and FRE sorbed analytes more slowly and to a lesser extent than the other materials tested.
As the study progressed, an increasing number of spurious peaks were found in the high performance liquid chromatography (HPLC) chromatograms of some of our samples, indicating that leaching of some consituents had occurred. By the end of the study, there were 11 additional peaks in the ABS samples, five in the FRP samples, and one in the FRE samples. Analysis by purge and trap gas chromatography/mass spectrometry (GC/MS) of those samples and of well water samples that were exposed to the casings for 500 hours revealed the identity of some of the leached constituents; acrylonitrile and styrene (components of ABS), chloroform and ethylbenzene (an intermediate in the production of styrene) from the ABS pipe, and toluene, 1,1,1-trichloroethane, and ethylbenzene from the FRP casing. 相似文献
13.
Ian Hers Reidar Zapf-Gilje Paul C. Johnson Loretta Li 《Ground Water Monitoring & Remediation》2003,23(2):119-133
Screening level models are now commonly used to estimate vapor intrusion for subsurface volatile organic compounds (VQCs). Significant uncertainty is associated with processes and models and, to date, there has been only limited field-based evaluation of models for this pathway. To address these limitations, a comprehensive evaluation of the Johnson and Ettinger (J&E) model is provided through sensitivity analysis, comparisons of model-predicted to measured vapor intrusion for 11 petroleum hydrocarbon and chlorinated solvent sites, and review of radon and flux chamber studies. Significant intrusion was measured at five of 12 sites with measured vapor attenuation ratios (αm 's) (indoor air/source vapor) ranging from ∼1 × 10−6 to 1 × 10−4 . Higher attenuation ratios were measured for studies using radon, inert tracers, and flux chambers; however, these ratios are conservative owing to boundary conditions and tracer properties that are different than those at most VOC-contaminated sites. Reasonable predictions were obtained using the J&E model with comparisons indicating that model-predicted vapor attenuation ratios (αp 's) were on the same order, or less than the αm 's. For several sites, the αm were approximately two orders of magnitude less than the αp 's indicating that the J&E model is conservative in these cases. The model comparisons highlight the importance in using appropriate input parameters for the J&E model. The regulatory implications associated with use of the J&E model to derive screening criteria are also discussed. 相似文献
14.
David M. Quanrud Konrad Quast Otakuye Conroy Martin M. Karpiscak Charles P. Gerba Kevin E. Lansey Wendell P. Ela Robert G. Arnold 《Ground Water Monitoring & Remediation》2004,24(2):86-93
The fate of estrogenic activity in waste water effluent was examined during surface transport and incidental recharge along the Santa Cruz River in Pima County, Arizona. Based on measurement of boron isotopes, the fractional contribution of reclaimed water in surface waters and ground water wells proximate to the river was determined for a contemporary sample set. Estrogenic activity decreased by −60% over the 25 mi length of the river below effluent discharge points in Tucson. In ground water samples obtained from monitoring wells that are proximate to the Santa Cruz River, both dissolved organic carbon ( p = 0.0003) and estrogenic activity ( p = 3 × 10−6 ) were highly correlated to fractional waste water content. Results indicate that proximate ground water quality is sensitive to incidental recharge of reclaimed water in the Santa Cruz River bed. In a few locations, little attenuation of estrogenic activity was apparent during percolation of effluent in the river channel to well withdrawal points. 相似文献
15.
Ian Hers Reidar Zapf-Gilje Paul C. Johnson Loretta Li 《Ground Water Monitoring & Remediation》2003,23(1):62-76
Screening level models are now commonly used to estimate vapor intrusion for subsurface volatile organic compounds (VOCs). Significant uncertainty is associated with processes and models and, to date, there has been only limited field-based evaluation of models for this pathway. To address these limitations, a comprehensive evaluation of the Johnson and Ettinger (J&E) model is provided through sensitivity analysis, comparisons of model-predicted to measured vapor intrusion for 11 petroleum hydrocarbon and chlorinated solvent sites, and review of radon and flux chamber studies. Significant intrusion was measured at five of 12 sites with measured vapor attenuation ratios (αm 's) (indoor air/source vapor) ranging from ∼1 × 10−6 to 1 × 10−4 . Higher attenuation ratios were measured for studies using radon, inert tracers, and flux chambers; however, these ratios are conservative owing to boundary conditions and tracer properties that are different than those at most VOC-contaminated sites. Reasonable predictions were obtained using the J&E model with comparisons indicating that model-predicted vapor attenuation ratios (αp 's) were on the same order, or less than the αm 's. For several sites, the (m were approximately two orders of magnitude less than the a 's indicating that the J&E model is conservative in these cases. The model comparisons highlight the importance in using appropriate input parameters for the J&E model. The regulatory implications associated with use of the J&E model to derive screening criteria are also discussed. 相似文献
16.
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 3 He/4 He and 4 He/20 Ne ratios of these samples. It was found that the 3 He/4 He 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 3 He/4 He 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 3 He/4 He 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
17.
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 SO4 2 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 SO4 2- ; was significantly concentrated at the anode. Over a period of approximately nine days, the concentration of SO4 2- 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
18.
《Ground Water Monitoring & Remediation》1986,6(3):92-98
A number of samples of polyvinyl chloride (PVC) well casings used for ground water monitoring that varied in schedule, diameter or manufacturer were placed in contact with low concentrations of aqueous solutions of TNT, RDX, HMX and 2,4-DNT for 80 days. Analysis indicated that there was more loss of TNT and HMX with the PVC casing than with the glass controls, but that the amount lost was, for the most part, equivalent among different types. A second experiment was performed to determine if these losses were due to sorption or if biodegradation was involved. Several different ground water conditions were simulated by varying salinity, initial pH and dissolved oxygen content. The only case where there was an in-creased loss of any substance due to the presence of PVC casing was with the TNT solution under non-sterile conditions. The extent of loss was small, however, considering the length of the equilibration period. This increased loss is thought to be associated with increased microbial degradation rather than sorption. Several samples of PVC casing were also leached with ground water for 80 days. No detectable interferences were found by reversed-phase high performance liquid chromatography (HPLC) analysis. Therefore, it is concluded that PVC well casings are suitable for monitoring ground water for the presence of these munitions. 相似文献
19.
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
20.
Comparison of Two Integrated Methods for the Collection and Analysis of Volatile Organic Compounds in Ground Water 总被引：1，自引：0，他引：1
Bradley M. Patterson Terry R. Power Chris Barber 《Ground Water Monitoring & Remediation》1993,13(3):118-123
The principal difficulties with determinations of volatile organic compounds (VOCs) in ground water are the reliability of sampling procedures and analytical methods. Two integrated methods have been developed for routine sampling, processing, and analysis of VOCs in ground water. These methods involve in situ collection of ground water using a modified syringe sampler from PVC piezometers or using dedicated glass syringes from stainless steel multilevel bores. The samples are processed in the syringe using purge and trap or microsolvent extraction and analyzed by GC/MSD.
The modified purge-and-trap method is time-consuming and limited to volatile organic compounds. However, it is extremely sensitive and flexible: the volume of sample used can be varied by the use of different-size glass syringes (sample volumes from 1 to 100 mL).
In cases where extremely low sensitivity (<10 mg 1−1 ) is not critical, the microextraction technique is a more cost-effective method, allowing twice as many samples to be analyzed in the same time as the purge-and-trap method. It enables less volatile compounds such as polynuclear aromatic hydrocarbons, phenol, and cresols to be analyzed in the same GC run. Also, the microextraction method can be used in the field to avoid delays associated with transportation of ground water samples to the laboratory. 相似文献
The modified purge-and-trap method is time-consuming and limited to volatile organic compounds. However, it is extremely sensitive and flexible: the volume of sample used can be varied by the use of different-size glass syringes (sample volumes from 1 to 100 mL).
In cases where extremely low sensitivity (<10 mg 1