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  • 1990-1994  (10)
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Environmental science & technology 28 (1994), S. 1650-1660 
    ISSN: 1520-5851
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Environmental science & technology 25 (1991), S. 1223-1237 
    ISSN: 1520-5851
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Environmental science & technology 26 (1992), S. 2301-2302 
    ISSN: 1520-5851
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Environmental science & technology 26 (1992), S. 2454-2461 
    ISSN: 1520-5851
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
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  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Environmental science & technology 25 (1991), S. 1237-1249 
    ISSN: 1520-5851
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Environmental science & technology 27 (1993), S. 2141-2148 
    ISSN: 1520-5851
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1745-6584
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Geosciences
    Notes: Results are presented that demonstrate the in-situ biotransformation of vinyl chloride (VC), trans-l,2-dichloroethylene (t-DCE), cis-l,2-dichloroethylene (c-DCE), and trichloroethylene (TCE) by an enhanced population of methane-utilizing (methanotrophic) bacteria. Biostimulation was accomplished by introducing dissolved methane and oxygen into a shallow, confined aquifer, to encourage the growth of the native methanotrophic bacteria. Biotransformation of the target compounds ensued immediately after the commencement of methane utilization, and reached steady-state values within three weeks. The approximate extents of transformation achieved in the two meter biostimulated zone were as follows: VC, 95%; t-DCE, 90%; c-DCE, 50%; and TCE, 20%. The biotransformation of VC and t-DCE was observed to be competitively inhibited by methane. Cyclic variations in methane concentration caused by the alternate pulse injection of dissolved methane into the test zone caused oscillations of the aqueous concentrations of VC and t-DCE. When formate and methanol were substituted for methane as alternative electron donors, inhibition ceased (no oscillations), and concentrations were reduced to levels achieved during periods when no methane was present, confirming the inhibition by methane. Higher transformation rates were achieved temporarily, i.e., for several days, through the addition of formate or methanol. When electron donor addition was terminated, the concentration of target compounds rapidly increased, indicating that the transformation promptly ceased. Although these experiments indicated that methane competitively inhibits transformation rates, this competition is a second-order effect: methane as substrate for growth was also required for transformation of VC, t-DCE, c-DCE, and TCE by methanotrophs.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1745-6584
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Geosciences
    Notes: Careful site characterization and implementation of quantitative monitoring methods are prerequisites for a convincing evaluation of enhanced biostimulation for aquifer restoration. This paper describes the characterization of a site at Moffett Naval Air Station, Mountain View, California, and the implementation of a data acquisition system suitable for real-time monitoring of subsequent aquifer restoration experiments. A shallow, confined aquifer was chosen for the enhanced biodegradation demonstration, and was shown to have suitable hydraulic and geochemical characteristics. Injection and extraction wells were installed at a distance of 6 m, with intermediate monitoring wells at distances of 1, 2.2, and 4 meters from the injection well. Bromide tracer tests revealed travel times of S to 27 hours from the injection well to the various monitoring wells, and 20 to 42 hours from the injection well to the extraction well. Complete breakthrough of the tracer at the monitoring wells was facilitated by choosing a line of wells aligned with the regional flow, and selecting injection and extraction flow rates of approximately 1.5 and 10 liters/min. Transport studies were conducted with selected halogenated organic compounds. The retardation factors were found to range from approximately 2 to 12. The breakthrough responses for the more strongly sorbing compounds, e.g. TCE, exhibited pronounced tailing, such that a minimum period of several weeks was required to achieve complete saturation of the aquifer. The microcomputer-driven sampling, analysis and data management system provided automated data acquisition at sample intervals of 40 minutes, with coefficients of variation smaller than 20%, and allowed for real-time surveillance of the dynamic responses. Overall, the conditions were favorable for a quantitative evaluation of in-situ aquifer restoration by enhanced biodegradation.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1745-6584
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Geosciences
    Notes: Results are presented from a field study that document the in-situ biotransformation of trichloroethylene (TCE), cis-dichLoroethylene (cis-DCE), trans-dichloroethylene (trans-DCE), and vinyl chloride (VC) in a saturated, semiconfined aquifer. The enhanced biotransformation was accomplished by stimulating the growth of indigenous methane-oxidizing bacteria (methanotrophs), which transform chlorinated aliphatic compounds by a cometabolic process to stable, nontoxic end products. Experiments were performed in the presence and absence of biostimulation by means of controlled chemical addition, frequent sampling, and quantitative analysis. The degree of biotransformation was assessed using mass balances and comparisons with bromide as a conservative tracer. Biostimulation of the test zone was successfully achieved by injecting methane- and oxygen-containing ground water in alternating pulses under induced gradient conditions. After a few weeks of stimulation, methane concentrations gradually decreased below the detection limit within two meters of travel. Under active biostimulation conditions, 20 to 30% of the TCE was biotransformed during the first season of testing. Direct evidence for biotransformation of VC, trans-DCE, cis-DCE, and TCE was obtained in the second and third seasons of field testing. In the absence of biostimulation, the organic compounds concentrations at observation wells reached 95% of the injection concentration, demonstrating negligible losses due to abiotic processes. Biostimulation of the test zone resulted in a concurrent decrease in concentration of methane and the halogenated aliphatic compounds. The organic compounds were transformed within two meters of travel as follows: TCE, 20–30%; cis-DCE, 45–55%; trans-DCE, 80–90%; and VC, 90–95%. These results are in qualitative agreement with methane-utilizing, mixed-culture laboratory studies which indicate that the rate of biotransformation is more rapid when the molecules are less halogenated.A biotransformation intermediate was observed which was identified by GC-MS analysis as trans-dichloroethylene oxide (trans-DCE epoxide), an expected intermediate based on laboratory studies. When methane addition was stopped, the concentration of the intermediate rapidly decreased, while halogenated compound concentrations slowly increased, indicating that active methane utilization was required for biotransformation to occur.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1573-1634
    Keywords: Moment analysis ; sorbing solute transport ; spatially-periodic retardation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Technology
    Notes: Abstract Taylor-Aris dispersion theory, as generalized by Brenner, is employed to investigate the macroscopic behavior of sorbing solute transport in a three-dimensional, hydraulically homogeneous porous medium under steady, unidirectional flow. The porous medium is considered to possess spatially periodic geochemical characteristics in all three directions, where the spatial periods define a rectangular parallelepiped or a unit-element. The spatially-variable geochemical parameters of the solid matrix are incorporated into the transport equation by a spatially-periodic distribution coefficient and consequently a spatially-periodic retardation factor. Expressions for the effective or large-time coefficients governing the macroscopic solute transport are derived for solute sorbing according to a linear equilibrium isotherm as well as for the case of a first-order kinetic sorption relationship. The results indicate that for the case of a chemical equilibrium sorption isotherm the longitudinal macrodispersion incorporates a second term that accounts for the eflect of averaging the distribution coefficient over the volume of a unit element. Furthermore, for the case of a kinetic sorption relation, the longitudinal macrodispersion expression includes a third term that accounts for the effect of the first-order sorption rate. Therefore, increased solute spreading is expected if the local chemical equilibrium assumption is not valid. The derived expressions of the apparent parameters governing the macroscopic solute transport under local equilibrium conditions agreed reasonably with the results of numerical computations using particle tracking techniques.
    Type of Medium: Electronic Resource
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