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571.
Quick-look assessments to identify optimal CO2 EOR storage sites 总被引:1,自引:0,他引:1
Vanessa Núñez-López Mark H. Holtz Derek J. Wood William A. Ambrose Susan D. Hovorka 《Environmental Geology》2008,54(8):1695-1706
A newly developed, multistage quick-look methodology allows for the efficient screening of an unmanageably large number of
reservoirs to generate a workable set of sites that closely match the requirements for optimal CO2 enhanced oil recovery (EOR) storage. The objective of the study is to quickly identify miscible CO2 EOR candidates in areas that contain thousands of reservoirs and to estimate additional oil recovery and sequestration capacities
of selected top options through dimensionless modeling and reservoir characterization. Quick-look assessments indicate that
the CO2 EOR resource potential along the US Gulf Coast is 4.7 billion barrels, and CO2 sequestration capacity is 2.6 billion metric tons. In the first stage, oil reservoirs are screened and ranked in terms of
technical and practical feasibility for miscible CO2 EOR. The second stage provides quick estimates of CO2 EOR potential and sequestration capacities. In the third stage, a dimensionless group model is applied to a selected set
of sites to improve the estimates of oil recovery and storage potential using appropriate inputs for rock and fluid properties,
disregarding reservoir architecture and sweep design. The fourth stage validates and refines the results by simulating flow
in a model that describes the internal architecture and fluid distribution in the reservoir. The stated approach both saves
time and allows more resources to be applied to the best candidate sites. 相似文献
572.
The aim of this interdisciplinary study is to examine a component of the hydrological cycle in Galapagos by characterizing
soil properties. Nine soil profiles were sampled on two islands. Their physical and hydrodynamic properties were analyzed,
along with their mineralogical composition. Two groups of soils were identified, with major differences between them. The
first group consists of soils located in the highlands (>350 m a.s.l.), characterized by low hydraulic conductivity (<10−5 m s−1) and low porosity (<25%). These soils are thick (several meters) and homogeneous without coarse components. Their clay fraction
is considerable and dominated by gibbsite. The second group includes soils located in the low parts of the islands (<300 m
a.s.l.). These soils are characterized by high hydraulic conductivity (>10−3 m s−1) and high porosity (>35%). The structure of these soils is heterogeneous and includes coarse materials. The physical properties
of the soils are in good agreement with the variations of the rainfall according to the elevation, which appears as the main
factor controlling the soil development. The clayey alteration products constrain soils physical and hydrodynamic properties
by reducing the porosity and consequently the permeability and also by increasing water retention. 相似文献
573.
The Cu–Co–Ni Texeo mine has been the most important source of Cu in NW Spain since Roman times and now, approximately 40,000 m3 of wastes from mine and metallurgical operations, containing average concentrations of 9,263 mg kg−1 Cu, 1,100 mg kg−1 As, 549 mg kg−1 Co, and 840 mg kg−1 Ni, remain on-site. Since the cessation of the activity, the abandoned works, facilities and waste piles have been posing
a threat to the environment, derived from the release of toxic elements. In order to assess the potential environmental pollution
caused by the mining operations, a sequential sampling strategy was undertaken in wastes, soil, surface and groundwater, and
sediments. First, screening field tools were used to identify hotspots, before defining formal sampling strategies; so, in
the areas where anomalies were detected in a first sampling stage, a second detailed sampling campaign was undertaken. Metal
concentrations in the soils are highly above the local background, reaching up to 9,921 mg kg−1 Cu, 1,373 mg kg−1 As, 685 mg kg−1 Co, and 1,040 mg kg−1 Ni, among others. Copper concentrations downstream of the mine works reach values up to 1,869 μg l−1 and 240 mg kg−1 in surface water and stream sediments, respectively. Computer-based risk assessment for the site gives a carcinogenic risk
associated with the presence of As in surface waters and soils, and a health risk for long exposures; so, trigger levels of
these elements are high enough to warrant further investigation. 相似文献
574.
Regional distribution pattern of groundwater heavy metals resulting from agricultural activities 总被引:18,自引:0,他引:18
Contaminations of groundwater by heavy metals due to agricultural activities are growing recently. The objective of this study
was to evaluate and map regional patterns of heavy metals (Cd, Zn and Cu) in groundwater on a plain with high agricultural
activities. The study was conducted to investigate the concentration of heavy metals and distribution in groundwater in regions
of Shush Danial and Andimeshk aquifers in the southern part of Iran. Presently, groundwater is the only appropriate and widely
used source of drinking water for rural and urban communities in this region. The region covers an area of 1,100 km2 between the Dez and Karkhe rivers, which lead to the Persian Gulf. For this study, the region was divided into four sub-regions
A, B, C and D. Additionally, 168 groundwater samples were collected from 42 water wells during the earlier months of 2004.
The flame atomic absorption spectrometry (AAS-Flame) was used to measure the concentration of heavy metals in water samples
and the Surfer software was used for determination of the contour map of metal distribution. The results demonstrated that
in all of the samples, Cd and Zn concentrations were below the EPA MCLG and EPA secondary standard, respectively. However,
the Cu contents of 4.8 % of all samples were higher than EPA MCL. It is also indicated that the concentrations of metals were
more pronounced at the southern part of the studied region than at the others. The analysis of fertilizers applied for agricultural
activities at this region also indicated that a great majority of the above-mentioned heavy metals were discharged into the
environment. Absence of confining layers, proximity to land surface, excess agricultural activities in the southern part and
groundwater flow direction that is generally from the north to the southern parts in this area make the southern region of
the Shush plain especially vulnerable to pollution by heavy metals than by other contaminants. 相似文献
575.
A Triassic carbonate unit has been intensively drained by zinc and lead ore mines and numerous borehole fields since the nineteenth
century. Its groundwater recharge has increased due to: pumping of water from boreholes, mining activity, and urbanization.
An approach to determine the amounts of the recharge at a variety of spatial scales is presented in the paper. Different methods
were used to identify and quantify recharge components on a regional and local scale: mathematical modelling was performed
for four aquifers included in an aquifer system, an analytical estimation based on the assumption that an average recharge
is equal to the average discharge of the hydrogeological system—for six man-made drainage centres, and the method of water
level fluctuation (WLF) was applied in one observation borehole. Results of modelling have been supplemented by observation
of environmental tracers (δ18O, δ2H, 3H), noble gases temperatures, and 4Heexc in groundwater. The regional aquifer’s current recharge according to estimations performed by means of modelling varies from
39 to 101 mm/year on average. Depending on the aquifer site the average precipitation ranges from 779 to 864 mm/year. In the
confined part of the aquifer average recharge ranges from 26 to 61 mm/year. Within outcrops average recharge varies from 96
to 370 mm/year. Current recharge estimated by the analytical method for man-made drainage centres varies from 158 up to 440 mm/year.
High values are caused by different recharge sources like precipitation, induced leakage from shallow aquifers, and water
losses from streams, water mains and sewer systems. Pumping of water, mining and municipal activities constitute additional
factors accounting for the intensified recharge. 相似文献
576.
Spatial data for landslide susceptibility, hazard, and vulnerability assessment: An overview 总被引:30,自引:0,他引:30
The aim of this paper is to discuss a number of issues related to the use of spatial information for landslide susceptibility, hazard, and vulnerability assessment. The paper centers around the types of spatial data needed for each of these components, and the methods for obtaining them. A number of concepts are illustrated using an extensive spatial data set for the city of Tegucigalpa in Honduras. The paper intends to supplement the information given in the “Guidelines for Landslide Susceptibility, Hazard and Risk Zoning for Land Use Planning” by the Joint ISSMGE, ISRM and IAEG Technical Committee on Landslides and Engineered Slopes (JTC-1). The last few decades have shown a very fast development in the application of digital tools such as Geographic Information Systems, Digital Image Processing, Digital Photogrammetry and Global Positioning Systems. Landslide inventory databases are becoming available to more countries and several are now also available through the internet. A comprehensive landslide inventory is a must in order to be able to quantify both landslide hazard and risk. With respect to the environmental factors used in landslide hazard assessment, there is a tendency to utilize those data layers that are easily obtainable from Digital Elevation Models and satellite imagery, whereas less emphasis is on those data layers that require detailed field investigations. A review is given of the trends in collecting spatial information on environmental factors with a focus on Digital Elevation Models, geology and soils, geomorphology, land use and elements at risk. 相似文献
577.
578.
A. A. Krylov O. M. Khlystov T. I. Zemskaya H. Minami A. Hachikubo H. Shoji M. Kida T. P. Pogodaeva L. Naudts J. Poort 《Geochemistry International》2008,46(10):985-995
This paper presents data on authigenic siderite first found in surface sediments from mud volcanoes in the Central (K-2) and Southern (Malen’kii) basins of Lake Baikal. Ca is the predominant cation, which substitutes Fe in the crystalline lattice of siderite. The enrichment of the carbonates in the 13C isotope (from +3.3 to +6.8‰ for the Malen’kii volcano and from +17.7 to +21.9‰ for K-2) results from the crystallization of the carbonates during methane generation via the bacterial destruction of organic matter (acetate). The overall depletion of the carbonates in 18O is mainly inherited from the isotopic composition of Baikal water. 相似文献
579.
Jürgen Konzett Daniel J. Frost Alexander Proyer Peter Ulmer 《Contributions to Mineralogy and Petrology》2008,155(2):215-228
Experiments have been conducted in the P-T range 2.5–15 GPa and 850–1,500°C using bulk compositions in the systems SiO2–TiO2–Al2O3–Fe2O3–FeO–MnO–MgO–CaO–Na2O–K2O–P2O5 and SiO2–TiO2–Al2O3–MgO–CaO–Na2O to investigate the Ca-Eskola (CaEs Ca0.5□0.5AlSi2O6) content of clinopyroxene in eclogitic assemblages containing garnet + clinopyroxene + SiO2 ± TiO2 ± kyanite as a function of P, T, and bulk composition. The results show that CaEsss in clinopyroxene increases with increasing T and is strongly bulk composition dependent whereby high CaEs-contents are favoured by bulk compositions with high normative
anorthite and low diopside contents. In this study, a maximum of 18 mol% CaEsss was found at 6 GPa and 1,350°C in a kyanite-eclogite assemblage garnet + clinopyroxene + kyanite + rutile + coesite. By comparison,
no significant increase in CaEsss with increasing P could be observed. If the formation of oriented SiO2-rods frequently observed in eclogititc clinopyroxenes is due to the retrogressive breakdown of a CaEs-component then these
textures are a cooling rather than a decompression phenomenon and are most likely to be found in kyanite-bearing eclogites
cooled from temperatures ≥750°C. The presence of clinopyroxene with approx. 4 mol% CaEsss in an experiment conducted at 2.5 GPa/850°C confirms earlier suggestions based on field data that vacancy-rich clinopyroxenes
are not necessarily restricted to ultrahigh pressure metamorphic conditions.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
580.
Pedro J. Marenco Frank A. Corsetti Douglas E. Hammond Alan J. Kaufman David J. Bottjer 《Chemical Geology》2008,247(1-2):124-132
The sulfur isotopic composition of carbonate associated sulfate (CAS) has been used to investigate the geochemistry of ancient seawater sulfate. However, few studies have quantified the reliability of δ34S of CAS as a seawater sulfate proxy, especially with respect to later diagenetic overprinting. Pyrite, which typically has depleted δ34S values due to authigenic fractionation associated with bacterial sulfate reduction, is a common constituent of marine sedimentary rocks. The oxidation of pyrite, whether during diagenesis or sample preparation, could thus adversely influence the sulfur isotopic composition of CAS. Here, we report the results of CAS extractions using HCl and acetic acid with samples spiked with varying amounts of pyrite. The results show a very strong linear relationship between the abundance of fine-grained pyrite added to the sample and the resultant abundance and δ34S value of CAS. This data represents the first unequivocal evidence that pyrite is oxidized during the CAS extraction process. Our mixing models indicate that in samples with much less than 1 wt.% pyrite and relatively high δ34Spyrite values, the isotopic offset imparted by oxidation of pyrite should be much less than ? 4‰. A wealth of literature exists on the oxidation of pyrite by Fe3+ and we believe this mechanism drives the oxidation of pyrite during CAS extraction, during which the oxygen used to form sulfate is taken from H2O, not O2. Consequently, extracting CAS under anaerobic conditions would only slow, but not halt, the oxidation of pyrite. Future studies of CAS should attempt to quantify pyrite abundance and isotopic composition. 相似文献