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PSHydrogeologic Analysis of the Oriskany Sandstone of the Appalachian Basin: Implication for Large-Scale Geologic Storage of CO2*
Jamie C. Skeen1 and Timothy R. Carr1
Search and Discovery Article #80056 (2009)
Posted September 25, 2009
* Adapted from poster presentation at AAPG Annual Convention and Exhibition, Denver, Colorado, USA, June 7-10, 2009.
1Geology, West Virginia University, Morgantown, WV. ([email protected])
The Oriskany Sandstone of the Appalachian basin is a widely distributed saline aquifer which has produced large quantities of hydrocarbons. Currently the Oriskany is host to numerous gas storage fields and is a potential target for large-scale geologic storage of CO2. Published and unpublished data of rock characteristics, pressure, temperature, and formation water geochemistry along with new brine samples were integrated within a geographical information system to better understand the regional-scale hydrogeological regime and its relation to the migration of hydrocarbons and geologic CO2 sequestration potential. The topographically driven up-dip flow of the Oriskany Sandstone formation waters is generally controlled by outcrops at high elevation to the east and at low elevation to the west. The up-dip flow is opposed by increased salinity induced buoyancy forces down-dip. The flow pattern is substantiated by the salinity distributions, with relatively lower salinity at recharge to the east and discharge to the west due to mixing with fresh meteoric water and higher salinity between the recharge and discharge zones. This flow pattern is also substantiated by the distribution of Oriskany gas fields that occur in the Central Appalachian basin; the major productive gas fields occur at the boundary between lower salinity and are typically absent in areas of higher salinity. It is believed that hydrocarbon distribution is influenced by basinal variations in buoyancy and entrainment by the formation water flow. Improved containment of large-scale CO2 injection appears to be associated in the Oriskany with convergent flow located in the eastern Appalachian basin.
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The Appalachian basin is approximately 500 kilometers wide and 1,000 km long. It encompasses a broad area between the Canadian Shield to the north, the Allegheny front to the east and the Cincinnati arch to the west (UTBEG, 2008). It represents part of an ancient foreland basin in the eastern United States that contains complex geology formed by a series of continental plate collisions. This deformation resulted in the formation of the Appalachian Mountains and large areas of stretched, faulted, and deformed ridges and valleys (USGS, 2008; UTBEG, 2008). The axis of the Appalachian basin is underlain by a succession of strata greater than 3000 meters thick (UTBEG, 2008). (Figure 1) Overlying a major interregional unconformity in the Appalachian basin is the Oriskany Sandstone, a widespread gas reservoir and saline formation The Oriskany Sandstone of the Appalachian basin represents the Deerpark stage of the Early Devonian (Diecchio, 1985). The sandstone is typically a fossiliferous quartz arenite cemented with quartz or calcite. It can be traced continuously through New York, Pennsylvania, Ohio, Maryland, West Virginia, Virginia, and Kentucky (Diecchio, 1985; Bruner and Smosna, 2008). The Oriskany typically overlies strata of Helderberg-age limestone or equivalents, and is overlain by Onondaga-age strata, which vary from limestone to chert to shale and are locally sandy (Diecchio, 1985). Since the Oriskany is a major deep gas producer within the basin data such as pressure, temperature, porosity, permeability, and brine composition are available (Diecchio et al., 1984). The data indicate that there exists intergranular and fracture porosity within the Oriskany, and thick low-permeability zones within the Appalachian basin with the potential for containment (Diecchio, 1984; Gupta et al., 2005).
As part of the effort by the National Energy Technology Laboratory (NETL) of the US Department of Energy and the Regional Carbon Sequestration Partnerships (RCSPs), data was assembled to address questions of carbon capture and storage (CCS). Data on sources and potential geologic storage sites were collected and organized for the construction of the Carbon Sequestration Atlas of the United States and Canada (http://www.netl.doe.gov/technologies/carbon_seq/refshelf/atlas/index.html).
Saline formations are natural salt-water bearing intervals of
porous and permeable rocks that occur beneath the level of potable
groundwater (<10,000 mg/l by SDWA standards). A number of the saline
formations in the Appalachian basin are used for gas storage and waste-fluid
disposal. Saline formations are much more extensive than coal seams or oil-
and gas-bearing rock, and represent an enormous potential for CO2
geologic storage. However, much less is known about saline formations,
because they lack the characterization experience that industry has acquired
through resource recovery from oil and gas reservoirs and coal seams.
Therefore, there is a greater amount of uncertainty regarding the suitability
of saline formations for CO2 storage. In order to maintain the
injected CO2 in a supercritical phase (i.e. super-critical liquid)
the geologic unit must be approximately 2,500-feet or greater in
While not all saline formations in the U.S have been examined, the RCSPs have documented the locations of such formations with an estimated sequestration potential ranging from 3,300 to more than 12,200 billion metric tons of CO2. (Figure 4) As a result of the inclusion of new evaluations from the Gulf Coast and other areas, identified potential for CO2 geologic storage in saline formations has increased approximately 2,000 to 9,000 billion metric tons from the previous version of the Atlas.
There are two types of carbon dioxide (CO2) emission sources: stationary sources and non-stationary sources. Non-stationary source emissions include CO2 emissions from the transportation sector. Stationary source emissions come from a particular, identifiable, localized source, such as a power plant. CO2 from stationary sources can be separated from stack gas emissions and subsequently transported to a geologic storage injection site. The “North American CO2 Sources” map displays the location and relative magnitude of a variety of CO2 stationary sources. (Figure 5)
According to the EPA, in 2006, total U.S. GHG emissions were estimated at 7,054.2 million metric tons CO2 equivalent. This estimate included CO2 emissions as well as other GHGs such as methane (CH4), nitrous oxide (N2O), and hydrofluorocarbons (HFCs). Annual GHG emissions from fossil fuel combustion primarily CO2 were estimated at 5,637.9 million metric tons with 3,781.9 million metric tons from stationary sources. While not all potential GHG sources have been examined, NETL’s RCSPs through the NatCarb effort have documented the location of more than 4,796 stationary sources with total annual emissions of 3,276 million metric tons of CO2. The concentration of major CO2 sources in the Appalachian basin is one of the highest in North America. The Midwest Regional Carbon Sequestration Partnership has estimated that the area generates almost 21 percent of our country’s electricity, 78 percent of which is from coal.
The northern Appalachian basin is an elongate, asymmetric
foreland basin with a preserved northeast-southwest trending central axis
that extends through Pennsylvania, western Maryland, and West Virginia. The
eastern margin of the basin is concealed beneath thrust sheets in the Blue Ridge Province of the Appalachian Mountains. The western margin of the basin
occurs in east-central Kentucky and central Ohio. The Cincinnati and Findlay arches
separate the Appalachian basin from the Illinois and Michigan basins.
Following Cambrian (Iapetan) rifting, the basin was enlarged by periodically
reactivation of geologic structures that developed in response to collisional
tectonics along the eastern margin of North America during the Taconic (Upper
Ordovician), Acadian (Middle to Upper Devonian), and Alleghany (Upper
Carboniferous) orogenies of the Paleozoic Era (Tankard, 1986; Quinlan and
Beaumont, 1984; Thomas, 1995; Shumaker, 1996). The structure on the Oriskany
Sandstone forms a surface that dips toward the center of the Appalachian
basin forming a northeast-southwest trend. At the center of the study area
the Oriskany Sandstone reaches a subsea
The Oriskany Sandstone reaches depths of over 2,500 meters along a northeast-southwest trend in the center of the Appalachian basin. It shallows toward the Eastern Overthrust Belt which coincides with the know outcrop area at the east of the basin. The Oriskany gradually shallows toward the Cincinnati Arch to the west in Ohio where it subcrops or outcrops at ground level. (Figure 7)
Bottom-hole temperatures (BHTs) are recorded during logging of
the borehole and commonly are not at equilibrium with formation temperature
and require correction. In general, BHTs from shallow boreholes are too high,
and BHTs from deep boreholes are too low. One method to correct the BHT
values is to plot them versus
Oriskany temperature = 0.0195 x (
Corrected BHTs were used to construct a map of subsurface temperature of the Oriskany Sandstone. (Figure 8) The Low Plateau and High Plateau of the central Appalachian basin are the deepest and hottest areas.
The thickness of the Oriskany Sandstone varies across the Appalachian basin from zero in the “no sand” area to a thickness of over 75 meters. It is typically thickest in the High Plateau and Eastern Overthrust Belt regions. The Oriskany thins to the west, northwest and to the south, where it is generally less than 12 meters thick. (Figure 9)
Under hydrostatic groundwater conditions, pressure increases
with
Previously analyzed core data were used to estimate the porosity of the Oriskany Sandstone. The data was limited to areas of existing oil and gas fields, and therefore mapping based on these data was spatially extrapolated across data gaps within the study area. The core scale porosity measurements were scaled up to well scale and then to basin scale using the method described by Bachu and Underschultz (1992, 1993). The method states that the formation-scale porosity index (Φ) of the unit is the arithmetic average of the core-scale values weighted by the thickness of the unit. A total of 803 wells were assigned values and a mean of 8.08% porosity was calculated. The Low Plateau and High Plateau of the central Appalachian basin are the deepest and contain the area with the lowest porosity values. (Figure 11)
Existing brine geochemical data were gathered from published and unpublished state and federal geological surveys, as well as local oil and gas companies. Additional brine samples were collected from existing oil and gas wells distributed throughout the Appalachian basin, with an attempt made to locate the sample sites where know data was lacking. Across the extent of the Oriskany Sandstone the TDS ranges from freshwater (TDS < 10,000 mg/L) to dense brine (TDS > 300,000 mg/L). The brine samples were characterized by large differences between the reported TDS concentrations from neighboring wells within the same gas field. The cause of these differences may be related to areal, vertical, and temporal variability, errors introduced from sampling procedures, or to varying methods of chemical analysis (Jorgensen, et al., 1993). The dense brines are concentrated in the Oriskany structural lows at the center of the basin. The relatively lower TDS concentrations are associated with the recharge area along the outcrop area to the east and the discharge area to the west. (Figure 12)
Formation waters associated with microbial gas have low Ca/Mg ratios (<2) associated with high alkalinity values from calcite precipitation, induced by microbial methanogenesis (Martini et al., 1998). The ratio of calcium concentration to magnesium concentration for the Oriskany Sandstone across the Appalachian basin is generally less than ten. The ratio is typically lower at the recharge area to the east and the discharge area to the west, with values less than five. The ratio is generally higher in the northeast area of the basin, reaching values of up to 30. (Figure 13)
Temperature and pressure conditions must be adequate to keep
injected CO2 in the dense supercritical or liquid phase (at its
critical point for CO2, its temperature Tc is 31.1°C and Pc is
7.83 megapascals, or MPa), this is usually interpreted as a
Map of contours reflecting levels of potential energy from high (Red) to low (Violet). (Figure 15) In a fluid environment, the controls on surface are hydraulic head values calculated from water saturated formation pore pressures. From the isopotential contours, flow paths and sinks can be inferred. Modified from Dahlberg, 1995.
Formation pressure was used to calculate equivalent freshwater hydraulic head Ho according to the formula
Ho = z + p / ρog
where z is elevation, p is pressure, ρo = 1000 kg/m3, and g is the gravitational constant (Bachu and Undershultz, 1993, 1995; Anfort et al., 2001). The density of formation waters in sedimentary basins, a function of temperature and salinity, is not equal to the density of freshwater and has the potential to introduce error (Bachu and Undershultz, 1993, 1995). An indication of the significance of this introduced error is given by the dimensionless driving force ratio (DFR) defined (Davies, 1987; Bachu, 1995) as:
DFR = Δρ|ΔE|/|ρo|ΔHo|h
where |ΔE| is the magnitude of the aquifer slope, |ΔHo|h is the magnitude of the horizontal component of the freshwater hydraulic-head gradient, Δρ is the difference between formation-water and freshwater densities. If the DFR value is greater than 0.5, neglecting buoyancy effects will introduce significant errors in flow analysis (Davies, 1987). Within the Oriskany Sandstone the values were generally much less than 0.5, with the exception of two areas located in south-central Pennsylvania . The distribution of freshwater hydraulic head shows the expected trends of northwestward and southeastward flow from the basin center toward the western subcrop area and the eastern outcrop area. (Figure 16) Use of freshwater hydraulic heads in the flow analysis of variable density formation waters may introduce significant errors, depending on interaction between the potential and buoyancy forces driving the flow. Hydraulic heads range from over 1000 m in the deeper part of the basin to less than 250 m at the recharge area to east and the discharge area to the west.
The Oriskany Sandstone of the Appalachian basin is a widely distributed saline aquifer which has produced large quantities of hydrocarbons. Using published and unpublished data of rock characteristics, pressure, temperature, and formation water geochemistry along with new brine samples were used to map the regional-scale hydrogeological regime and its relation to the migration of hydrocarbons and geologic CO2 sequestration potential. Basin-scale fluid flow of the Oriskany Sandstone formation waters is generally controlled by salinity differences and by differences in structural elevation. The flow pattern is substantiated by the salinity distributions and water geochemistry (Ca/Mg), with relatively lower salinity at recharge to the east and discharge to the west due to mixing with fresh meteoric water and higher salinity between the recharge and discharge zones. The basin-scale flow pattern is also substantiated by the distribution of oil and gas fields that occur in the Central Appalachian basin; the major productive gas fields occur at the boundary between lower salinity and are typically absent in areas of higher salinity. It is believed that hydrocarbon distribution is influenced by basinal variations in buoyancy and entrainment by the formation water flow. Improved containment of large-scale CO2 injection appears to be associated in the Oriskany with convergent flow located in the eastern Appalachian basin. Storage capacity for the Oriskany saline formation is estimated by the equation
GCO2 = A hg фtot ρ E
GCO2 = estimate of total saline formation storage capacity in grams A = area of basin greater than 800 meters in
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