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1.
Influence of Casing Materials on Trace-Level Chemicals in Well Water   总被引:1,自引:0,他引:1  
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   

2.
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   

3.
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   

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.
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   

6.
State-of-the-art analytical techniques are capable of detecting contamination In the part per billion (ppb) range or lower. At these levels, a truly representative ground water sample Is essential to precisely evaluate ground water quality. The design specifications of a ground water monitoring system are critical in ensuring the collection of representative samples, particularly throughout the long-term monitoring period.
The potential interfaces from commonly used synthetic well casings require a thorough assessment of site, hydrogeology and the geochemical properties of ground water. Once designed, the monitoring system must be installed following guidelines that ensure adequate seals to prevent contaminant migration during the installation process or at some time in the future. Additionally, maintaining the system so the wells are in hydraulic connection with the monitored zone as well as periodically Inspecting the physical integrity of the system can prolong the usefulness of the wells for ground water quality. When ground water quality data become suspect due to potential interferences from existing monitoring wells, an appropriate abandonment technique must be employed to adequately remove or destroy the well while completely sealing the borehole.
The results of an inspection of a monitoring system comprised of six 4-inch diameter PVC monitoring wells at a hazardous well facility Indicated that the wells were improperly installed and in some cases provided a pathway for contamination. Subsequent down hole television inspections confirmed inaccuracies between construction logs and the existing system as well as identified defects in casing materials. An abandonment program was designed which destroyed the well casings in place while simultaneously providing a competent seal of the re-drilled borehole.  相似文献   

7.
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   

8.
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   

9.
A suction side sample collector (SSSC) is a contrivance installed hydraulically ahead of the intake port of a pumping device. This paper describes construction and operational details of SSSCs fitted to a submersible pump with packer for use in a 6-inch cased borehole, an air lift pump with packer for use in a 1-inch or 2.5-inch cased borehole, a bladder pump for use in a casing of 2-inch or greater diameter, and a jet pump with packer for use in a 2-inch cased borehole.
Each form of SSSC has been thoroughly tested in ground water quality sampling for volatile organic chemicals. Comparative data for samples collected with the SSSCs and conventional sample collecting gear are presented. The SSSC is demonstrated to be superior to other methods of collecting volatile organic chemical samples owing to its freedom from contamination by the pump delivery line and to its mode of collecting the sample from a position in the well remote from disturbance by the pumping technique.
SSSCs are conveniently decontaminated, easily transported, and can be used to deliver samples to the laboratory while still at formation pressure. The air-lift pumps, described in this paper for use with SSSCs in 1- and 2.5-inch casings, have pumping capacities greater than obtained by other methods that can operate in these small casings. Discharge rates of up to 2 gpm are routinely achieved with the 1-inch model and higher rates are common With the 2.5-inch model. The use of packers with these pumps reduces the time needed to replace the water in the casing with fresh water from the formation.  相似文献   

10.
The objective of this study was to assess the possible impact of deep well disposal operations, conducted between 1958 and 1974, on the ground water quality in a shallow fresh water aquifer beneath Sarnia, Ontario, Canada. Because of the breakout of formation fluids in Sarnia and Port Huron, Michigan, in the early 1970s, it had been hypothesized that liquid waste from the disposal zone in bedrock had leaked through numerous abandoned oil, gas, and salt wells in the area up to the shallow fresh water aquifer and from there to the surface.
A monitoring well network of 29 5cm (2 inch) diameter piezometers was established in the thin sand and shale aquifer system, which exists between 30 and 70m (100 and 230 feet) below ground surface. In addition, a 300m (1000 foot) deep borehole was drilled and instrumented with a Westbay multilevel casing, which permitted sampling of the disposal zone.
Ground water samples from the shallow monitoring wells and the Westbay multilevel casing were analyzed for volatiles by GC/MS. Those volatile aromatics that were conspicuously present in the deep disposal zone, e.g., ethyl toluenes and trimethyl benzene, were not detected in the shallow monitoring wells. Thus, if contaminants from the disposal zone did indeed migrate to the shallow aquifer, contamination was not widespread and probably consisted mostly of displaced chloride-rich formation waters.  相似文献   

11.
Waste water from ammunition production sites and aqueous samples (ground and surface water) on or near former military sites on which explosives were produced or filled, e.g. into shells, may be contaminated by the original explosives—mainly nitrotoluenes (such as dinitrotoluenes, trinitrotoluene (TNT)) and nitramines (such as hexogen (RDX), octogen (HMX), and tetryl) or hexyl, but also by byproducts and compounds formed by biodegradation of the explosives such as aminonitrotoluenes, chlorinated nitrobenzenes and nitrophenols. These compounds can be extracted from aqueous samples by liquid/liquid extraction (using dichloromethane or toluene) or by solid phase extraction using C-18 adsorbents with high recoveries (usually ≥85%) provided they contain only one amino group. Nitrotoluenes, chlorinated nitrobenzenes and aminonitrotoluenes (nitrotoluidines) may be determined by gas chromatography (GC) using selective detectors such as an electron capture detector (ECD), a nitrogen-phosphorus detector (NPD) or a chemiluminescence detector (thermal energy analyzer, TEA). The use of combined gas chromatography/mass spectrometry (GC/MS) under electron impact conditions is even more specific. Detection limits comparable to an ECD or NPD, however, are only achieved if the mass spectrometer is operated under selected ion monitoring (SIM). Nitrophenols are derivatized after extraction by heptafluorobutyric anhydride or by acetic anhydride where the latter method can be directly applied to the aqueous sample. The nitramine explosives, such as RDX, HMX, and tetryl, hexyl, the nitrate esters, such as nitropenta (PETN) and nitroguanidine as well as picric acid cannot, or only with difficulty, be analyzed by gas chromatography. They may be determined by high performance liquid chromatography (HPLC) with UV-detection. The HPLC analysis can be extended to include also nitrotoluenes and nitroaminotoluenes.  相似文献   

12.
Laboratory experiments were conducted to measure the extent to which trace concentrations of radioactive materials would sorb on well construction materials and to assess the rapidity with which sorption would occur. The radionuclides employed in these studies were tritium, Cs-137, and Co-57, Solutions with trace concentrations of these radionuclides were contracted with casings of PVC, fiberglass-epoxy, stainless steel, carbon steel, and steel rods coated wtih expoy. The PVC showed no interaction with the tritium or Cs-137 during contact times of two hours to these weeks; however, it did sorb Co-57. The fiberglass-epoxy also interacted only with the cobalt. The stainless steel sorbed cesium and cobalt. The carbon steel (or the ferric hydroxide forming on its surface) also sorbed both cesium and cobalt. The epoxy-coated steel rods did not interact measurably with day of the radio-nuclides so long as the coating was intact. The sorption reactions generally were apparent after a few days of contact: in the case of carbon steel, they were detectable in a few hours.  相似文献   

13.
Experiments simulating the dynamics of compliance sampling via a monitoring well were performed to assess the effects of common well screen materials (rigid polyvinyl chloride, polytetrafluoroethylene, stainless steel 304. and stainless steel 316) on several metals and tri- chloroethylene (TCE) in ground water. This was achieved by using a continuous flow-through chamber system capable of exposing monitoring well screens to ground water for periods ranging from 0.25 to 8 hours. The findings of this study are more representative than static laboratory experiments for assessing the potential effects well casing materials have on ground water samples. Under dynamic flow conditions stainless steel 304 and 316 screens were found to influence solution concentrations of Pb, Cd, Cr, Ni, and Fe, while ground water TCE concentrations were not affected by any of the materials tested.  相似文献   

14.
Waste disposal sites with volatile organic compounds (VOCs) frequently contain contaminants that are present in both the ground water and vadose zone. Vertical sampling is useful where transport of VOCs in the vadose zone may effect ground water and where steep vertical gradients in chemical concentrations are anticipated. Designs for combination ground water and gas sampling wells place the tubing inside the casing with the sample port penetrating the casing for sampling. This physically interferes with pump or sampler placement. This paper describes a well design that combines a ground water well with gas sampling ports by attaching the gas sampling tubing and ports to the exterior of the casing. Placement of the tubing on the exterior of the casing allows exact definition of gas port depth, reduces physical interference between the various monitoring equipment, and allows simultaneous remediation and monitoring in a single well. The usefulness and versatility of this design was demonstrated at the Idaho National Engineering and Environmental Laboratory (INEEL) with the installation of seven wells with 53 gas ports, in a geologic formation consisting of deep basalt with sedimentary interbeds at depths from 7.2 to 178 m below land surface. The INEEL combination well design is easy to construct, install, and operate.  相似文献   

15.
A ground water monitoring program should include an investigation of all possible areas of concern. To be completely effective, the program should include soil sampling, soil analysis and water-quality examination of both the saturated and unsaturated zones. A well-tooled drill rig can take all the proper soil samples, perform all necessary tests and install a functional monitoring well. With the introduction of the fluoropolymer (Teflon(r)) sleeve lysimeter, a single monitoring well can be constructed to monitor both the saturated and unsaturated zones in one installation. The monitoring well screen and casing may also be completely constructed of fluoropolymer.
The sleeve lysimeter is designed with a threaded hollow inner diameter, allowing it to be attached between the joints of a casing string. This hollow I.D. acts as an extension of the casing; the lysimeter surrounds the casing. This creates an isolated vessel for sampling the vadose zone. Access to the screened monitoring well below is unaffected. Tests have shown that when properly installed, these porous fluoropolymer filter units can collect samples with no interaction between the filter and collected fluids.  相似文献   

16.
Previous site-specific studies designed to assess the impacts of unsewered subdivisions on ground water quality have relied on upgradient monitoring wells or very limited background data to characterize conditions prior to development. In this study, an extensive monitoring program was designed to document ground water conditions prior to construction of a rural subdivision in south-central Wisconsin. Previous agricultural land use has impacted ground water quality; concentrations of chloride, nitrate-nitrogen, and atrazine ranged from below the level of detection to 296 mg/L, 36 mg/L, and 0.8 microg/L, respectively, and were highly variable from well to well and through time. Seasonal variations in recharge, surface topography, aquifer heterogeneities, surficial loading patterns, and well casing depth explain observed variations in ground water chemistry. This variability would not have been detected if background conditions were determined from only a few monitoring wells or inferred from wells located upgradient of the subdivision site. This project demonstrates the importance of characterizing both ground water quality and chemical variability prior to land-use change to detect any changes once homes are constructed.  相似文献   

17.
Hydrogeologic and ground water quality data obtained from a gas-driven multilevel sampler system and a polyvinyl chloride (PVC) monitoring well nest with the same aquifer communication intervals are compared. All monitoring points are in close proximity to each other. The study was conducted at an eight-acre uncontrolled hazardous waste site. The site is located in an alluvial valley composed of approximately 40 feet of alluvium overlying shale bedrock. The ground water at the site is contaminated with various organic constituents. A ground water monitoring network consisting of 26 conventional monitoring wells, nine observation well points, and six multilevel gas-driven samplers was established to characterize the hydrogeologic regime and define the vertical and horizontal extent of contamination in the vicinity of the abandoned chemical plant. As part of this study, a multilevel monitoring system was installed adjacent to a well nest. The communication zones of the multilevel samplers were placed at the same elevation as the sand packs of the well nest. The multilevel sampler system and well nest are located in a contaminated area directly downgradient of the site. A comparison of the vertical head distribution and ground water quality was performed between the well nest and the multilevel sampling system. The gas-driven multilevel sampling system consists of three gas-driven samplers that monitor separate intervals in the unconsolidated materials. The well nest, composed of two PVC monitoring wells in separate boreholes, has the same communication interval as the other two gas-driven samplers. Hydraulic head information for each multilevel sampler was obtained using capillary tubing. This was compared with heads obtained from the well nest utilizing an electric water level indicator. Chemical analyses from the PVC and multilevel sampler wells were performed and compared with one another. The analyses included organic acids, base neutrals, pesticides, PCBs, metals, volatile organics, TOX, TOC, CN, pH and specific conductance.  相似文献   

18.
Hole stability problems occurring during construction of monitoring wells in coarse, unconsolidated alluvium can be overcome by using a drill-through casing driver mounted on a standard top-head drive rotary rig. Steel casing is driven contemporaneously with drilling, providing continuous hole stability. Samples of aquifer material and ground water can be taken at discrete depths as drilling proceeds. Monitoring well completion is accomplished by: (1) using the steel casing as an open-ended piezometer; (2) installing a telescoping well screen; (3) plugging the casing end and perforating desired intervals, (4) installing one or more smaller diameter wells, and then (5) pulling back the steel casing. Advantages of this drilling method include maintenance of hole stability during drilling and well completion, faster borehole construction time than traditional methods in coarse alluvial deposits and other poorly sorted formations, and collection of representative samples of the geologic formations and ground water; additionally, drilling fluids are not required.  相似文献   

19.
A device was developed to make fine-scale in situ measurements of formation and ground water conductivity at depths up to 10 meters in unconsolidated shallow aquifers. It consists of a casing that is left in place ("disposable") and a probe that slides down the center of the casing making readings or taking water samples through screened slots. The device is inexpensive, designed to be jetted into place, and intended for use in monitoring situations where drilling rigs and wireline logs are impractical. It offers, in principle, 10cm resolution of the conductivities and the formation factor as a function of time.
Results from three of these units installed across a landfill plume near North Bay, Ontario, demonstrate the usefulness of these kinds of measurements in a monitoring study, and the problems that can be encountered in a highly contaminated environment.  相似文献   

20.
Hollow-stem augers are a widely used drilling method for constructing monitoring wells in unconsolidated materials. The drilling procedures used when constructing monitoring wells with hollow-stem augers, however, are neither standardized nor thoroughly documented in the published literature.
Variations in drilling procedures and techniques may occur as a result of the: (1) type of auger drill equipment and formation samplers used; (2) hydrogeologic conditions at the site, especially where heaving sands occur; and (3) known or suspected presence of contaminated zones, where there is a potential for the vertical movement of contaminants within the borehole.
In a saturated zone in which heaving sands occur, changes in equipment and drilling techniques are required to provide a positive pressure head of water within the auger column. This may require the addition of clean water or other drilling fluid inside the augers.
When monitoring the quality of ground water below a known contaminated zone, hollow-stem auger drilling may not be advisable unless protective surface casing can be installed. Depending on the site hydrogeology, conventional hollow-stem auger drilling techniques alone may not be adequate for the installation of the protective surface casing. A hybrid drilling method may be needed that combines conventional hollow-stem auger drilling with a casing driving technique that advances the borehole and surface casing simultaneously.  相似文献   

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