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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Ground water monitoring & remediation 20 (2000), S. 0 
    ISSN: 1745-6592
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Geosciences
    Notes: Air sparging experiments were conducted in a laboratory column to investigate air flow and mass transfer behavior in different types of sand at different air injection rates. Methyl tertiary butyl ether (MTBE) was applied as a tracer, and by measuring the volatilization and the mean air content during the experiments, the air flow pattern and its influence on mass transfer were assessed. The experimental results showed large differences among the sand types. In fine sand, the mean air content was high and the volatilization of MTBE was rapid with total recovery after a few hours. In coarse sand, the mean air content was low and the volatilization of MTBE was limited. The results indicate two different air flow distributions. In fine-grained materials, a uniform air distribution can be expected compared to coarse-grained materials where isolated air channels will limit the mass transfer. Afterwards, the experiments were simulated using the numerical multiphase flow code T2VOC, and the results compared to those obtained in the laboratory. The experiments with fine sand were simulated well, while for coarser sand types the volatilization was highly overestimated. The differences between model and laboratory results were mainly attributed to the nonuniformity of the air saturation and the neglection of kinetics in the mass transfer formulation.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Ground water 36 (1998), S. 0 
    ISSN: 1745-6584
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Geosciences
    Notes: This paper provides the first experimental determination of the rates and distribution of transport of a dense, nonaqueous phase liquid (DNAPL) through a naturally bioporous and fractured clayey till deposit. Until now, assessment of DNAPL behavior in this type of deposit has relied on theoretical studies. Predictions of DNAPL transport have proven to be uncertain as a result of difficulties in measuring critical parameters such as DNAPL entry pressure and flow behavior in response to natural fracture/biopore apertures and the degree of interconnection of these structures. In the present investigation, the migration of free product trichloroethylene (TCE) was studied by means of two undisturbed clayey till columns (dimensions: 0.5 m diameter by 0.5 m long) under in situ effective soil stress conditions. The experiments revealed that transport of TCE was restricted to biopores in one column and fractures in another column, bypassing the low-permeability clayey matrix. Effective porosities of the columns, i.e., bio-pores and fractures, were two to three orders of magnitude lower than total porosities (25% and 32%, respectively, for the two columns), i.e., macropores and matrix. Single phase water flow rates through the columns at water-saturated conditions followed a linear relationship with hydraulic gradient. TCE flow could not be predicted from the single-phase calculations because of non-linearity observed between applied TCE injection heads and resulting TCE flow. TCE flow rates were 24 and 10.3 m/day at TCE gradients of 1.18 and 0.91, respectively. The observed flow rates indicate that in cases where vertical biopores or fractures fully penetrate clayey till aquitards, a low-viscosity DNAPL (e.g., TCE) may quickly enter underlying aquifers. The experiments further indicate that 100 liters of a low-viscosity DNAPL are sufficient to contaminate approximately 25 to 100 m3 of till material because of the small effective porosity constituted by the biopores and fractures.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Ground water monitoring & remediation 21 (2001), S. 0 
    ISSN: 1745-6592
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Geosciences
    Notes: This paper compares the results of biodegradation experiments with creosote compounds performed at different scales. The experiments include field observations, field experiments, large-scale intact laboratory column experiments, model fracture experiments, and batch experiments. Most of the experiments were conducted with till or ground water from the field site at Ringe on the island of Funen. Although the experiments were conducted on different scales, they revealed that some phenomena—e.g., an extensive biodegradation potential of several of the creosote compounds, the inhibitory influence of the pyrroles on the biodegradation of benzene, and the biodegradation of benzothiophene occurs only in the presence of a primary substrate. The experiments show that some biodegradation processes of organic compounds may be common to different microorganisms.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Ground water monitoring & remediation 17 (1997), S. 0 
    ISSN: 1745-6592
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Geosciences
    Notes: The occurrence of heteroaromatic compounds (NSO) and their degradation products in ground water at creosote-contaminated sites in Denmark was investigated. NSO are of special interest because of their high polarity, toxicity, and adverse organoleptic properties. In total, the content of about 50 organic tar compounds and the chemical redox parameters of ground water from three creosote-contaminated sites were determined.The organic contamination of ground water varied considerably between sites and wells with concentrations up to mg/L level. The major organic contaminants were NSO, phenols, and monoaromatic hydrocarbons, which are among the most water-soluble creosote compounds. High concentration (several μg/L) of these compounds were observed downgradient of the contamination source. Within a distance of 50 to 80 m from the source, the concentrations of most compounds were reduced significantly, often below detection limits. The NSO constituted from 0.1 percent to 73 percent of all organic compounds determined by gas chromatography (GC) with an increasing dominance downgradient of the source. Among the 17 studied NSO, carbazole, thiophene, benzothiophene, dibenzothiophene, benzofuran, and dibenzofuran were observed most frequently (detection frequency 〉 60 percent). High concentrations (〉100 μ/L) of some NSO such as benzothiophene, carbazole, hydroxyquinolines, and basic N-compounds were observed occasionally. Other recent studies on creosote contamination support the present observations of high ground water concentrations of basic N-compounds and the high detection frequency of the aforementioned NSO. However, unlike the other studies, we did observe thiophene (1-10 μg/L).
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Ground water monitoring & remediation 16 (1996), S. 0 
    ISSN: 1745-6592
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Geosciences
    Notes: Field data from 44 waste sites contaminated with creosote have been compiled in a database. The data from each site included geological and hydrogeological parameters and the concentrations of creosote compounds in the ground water at various distances from the pollution sources. The creosote compounds that were measured included mononuclear aromatic hydrocarbons and polynuclear aromatic hydrocarbons (PAH) and phenols. Already 50 m down-gradient of the creosote waste sites, 90 percent of the concentrations were from three to 50 times lower than at the source, and most of the median concentrations were below detection limit (0.1 to 0.5 μg/L). The maximum concentrations of benzene, toluene, and xylenes (BTX) and phenols were much lower under aerobic than under anaerobic conditions. Among the phenols, the xylenols (dimethylphenols) appear in higher concentrations under aerobic conditions than phenol and the cresols do. The highest concentrations found were of the same order of magnitude as the calculated solubilities found in the literature, except the chrysene and benz(a)pyrene concentrations, which were one to two orders of magnitude higher than the solubilities.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Biodegradation 4 (1993), S. 163-170 
    ISSN: 1572-9729
    Keywords: factorial analysis ; kinetics ; methane ; methanotrophs ; nutrients
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The effect of different mineral nutrients on the kinetics of methane biodegradation by a mixed culture of methanotrophic bacteria was studied. The substrate factors examined were ammonia, iron, copper, manganese, phosphate, and sulphide. The presence of iron in the growth medium had a strong effect on the yield coefficient. Yield coefficients up to 0.49 mg protein per mg methane were observed when iron was added at concentrations of 0.10–5.0 mg/l. Iron addition also increased the maximum methane utilization rate. The same effect was observed after addition of ammonium to a medium where nitrate was the only nitrogen source. The observed Monod constant for methane utilization increased with increasing concentration of ammonia. This shows that ammonia is a weak competitive inhibitor as observed by other researchers. Relatively high levels of both ammonia (70 mg/l) and copper (300 µg/l) inhibited the methane degradation, probably due to the toxic effect of copper-amine complexes.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1572-9729
    Keywords: Anaerobic degradability ; creosote ; denitrification ; heterocyclic compounds ; methanogenesis ; reducing agents ; soil slurries ; sulphate-reduction ; sulphide inhibition
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Degradation of four heterocyclic compounds was examined under nitrate-reducing, sulphate-reducing and methanogenic conditions. Soil samples from a creosote-polluted site in Denmark were used as inoculum. Indole and quinoline were degraded under all redox conditions with the highest degradation rates obtained under sulphate-reducing conditions. Benzothiophene and benzofuran were not degraded during the observation period of 100 days under any of the redox conditions. Indole and quinoline degrading cultures could be repeatedly transferred under all redox conditions, except for degradation of quinoline under sulphate-reducing conditions which was inhibited by sulphide at concentrations above 0.8 mM. Degradation of quinoline under methanogenic conditions was also inhibited by 3.2 mM sulphide used as a reducing agent, but sulphide had no inhibitory effect on the degradation of indole in methanogenic and sulphate-reducing soil slurries.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Biodegradation 7 (1996), S. 97-107 
    ISSN: 1572-9729
    Keywords: Aerobic degradation ; creosote compounds ; factorial design ; inhibition ; interactions ; toluene
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The inhibiting effect of 14 typical creosote compounds on the aerobic degradation of toluene was studied in batch experiments. Four NSO-compounds (pyrrole, 1-methylpyrrole, thiophene, and benzofuran) strongly inhibited the degradation of toluene. When the NSO-compounds were present together with toluene, little or no degradation of toluene was observed during 16 days of incubation, compared with a total removal of toluene within 4 days when the four compounds were absent. Indole (an N-compound) and three phenolic compounds (phenol, o-cresol, and 2,4-dimethylphenol) also inhibited the degradation of toluene, though the effect was much weaker that of the four NSO-compounds. O-xylene, p-xylene, naphthalene and 1-methylnaphthalene seemed to stimulate the degradation even though the influence was very weak. No effects of benzothiophene (an S-compound) and quinoline (an N-compound) were observed. Benzofuran (an O-compound) was identified as the compound that most inhibited the degradation of toluene. An effect could be detected even at low concentrations (40 μg/l).
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Biodegradation 7 (1996), S. 191-201 
    ISSN: 1572-9729
    Keywords: aerobic degradation ; benzene ; creosote ; factorial design ; heterocyclic compounds ; inhibition ; interactions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The inhibitory effect of creosote compounds on the aerobic degradation of benzene was studied in microcosm experiments. A total removal of benzene was observed after twelve days of incubation in microcosms where no inhibition was observed. Thiophene and benzothiophene, two heterocyclic aromatic compounds containing sulfur (S-compounds), had a significant inhibitory effect on the degradation of benzene, but also an inhibitory effect of benzofuran (an O-compound) and 1-methylpyrrole (a N-compound) could be observed, although the effect was weaker. The NSO-compounds also had an inhibitory effect on the degradation of p-xylene, o-xylene, and naphthalene, while they only had a weak influence on the degradation of 1-methylnaphthalene, o-cresol and 2,4-dimethylphenol. The phenolic compounds seemed to have a weak stimulating effect on the degradation of benzene whereas the monoaromatic hydrocarbons and the naphthalenes had no significant influence on the benzene degradation. The inhibitory effect of the NSO-compounds on the aerobic degradation of benzene could be identified as three different phenomena. The lag phase increased, the degradation rate decreased, and a residual concentration of benzene was observed in microcosms when NSO-compounds were present. The results show that NSO-compounds can have a potential inhibitory effect on the degradation of many creosote compounds, and that inhibitory effects in mixtures can be important for the degradation of different compounds.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1572-9729
    Keywords: bacteria ; degradation ; denitrification ; kinetics ; stoichiometry ; toluene
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Batch experiments were carried out to investigate the stoichiometry and kinetics of microbial degradation of toluene under denitrifying conditions. The inoculum originated from a mixture of sludges from sewage treatment plants with alternating nitrification and denitrification. The culture was able to degrade toluene under anaerobic conditions in the presence of nitrate, nitrite, nitric oxide, or nitrous oxide. No degradation occurred in the absence of Noxides. The culture was also able to use oxygen, but ferric iron could not be used as an electron acceptor. In experiments with14C-labeled toluene, 34%±8% of the carbon was incorporated into the biomass, while 53%±10% was recovered as14CO2, and 6%±2% remained in the medium as nonvolatile water soluble products. The average consumption of nitrate in experiments, where all the reduced nitrate was recovered as nitrite, was 1.3±0.2 mg of nitrate-N per mg of toluene. This nitrate reduction accounted for 70% of the electrons donated during the oxidation of toluene. When nitrate was reduced to nitrogen gas, the consumption was 0.7±0.2 mg per mg of toluene, accounting for 97% of the donated electrons. Since the ammonia concentration decreased during degradation, dissimilatory reduction of nitrate to ammonia was not the reductive process. The degradation of toluene was modelled by classical Monod kinetics. The maximum specific rate of degradation, k, was estimated to be 0.71 mg toluene per mg of protein per hour, and the Monod saturation constant, K s , to be 0.2 mg toluene/l. The maximum specific growth rate, μ max , was estimated to be 0.1 per hour, and the yield coefficient, Y, was 0.14 mg protein per mg toluene.
    Type of Medium: Electronic Resource
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