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| ==Gasification== | | ==Gasification== |
− | Gasification is the conversion of oil to gas resulting from thermal cracking. It primarily takes place during burial. If oil is spilled from a trap by gas displacement during gasification, the oil may occur in economic [[accumulation]]s updip along the migration pathway.<ref name=ch11r12>Gussow, W. C., 1954, [http://archives.datapages.com/data/bulletns/1953-56/data/pg/0038/0005/0800/0816.htm Differential entrapment of oil and gas: a fundamental principle]: AAPG Bulletin, vol. 38, p. 816–853.</ref> | + | Gasification is the conversion of oil to gas resulting from thermal [[cracking]]. It primarily takes place during burial. If oil is spilled from a trap by gas displacement during gasification, the oil may occur in economic [[accumulation]]s updip along the [[migration pathway]].<ref name=ch11r12>Gussow, W. C., 1954, [http://archives.datapages.com/data/bulletns/1953-56/data/pg/0038/0005/0800/0816.htm Differential entrapment of oil and gas: a fundamental principle]: AAPG Bulletin, vol. 38, p. 816–853.</ref> |
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| ==Predicting and recognizing gasification== | | ==Predicting and recognizing gasification== |
| The following characteristics can help us predict and recognize gasification. | | The following characteristics can help us predict and recognize gasification. |
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− | * Geohistory analysis with proper gasification kinetics can usually predict at what depth [[accumulation]]s have been gasified. | + | * Geohistory analysis with proper gasification [[kinetics]] can usually predict at what depth [[accumulation]]s have been gasified. |
− | * As a rule of thumb, oil should not be expected at subsurface temperatures > [[temperature::150°C]] or a maturation level much above 1.3% R<sub>o</sub>. Dry gas accumulations can occur at shallower depths, but oil is not likely at greater depths. | + | * As a rule of thumb, oil should not be expected at subsurface temperatures > [[temperature::150°C]] or a [[maturation]] level much above 1.3% R<sub>o</sub>. Dry gas accumulations can occur at shallower depths, but oil is not likely at greater depths. |
| * Gasification of oil in reservoirs is associated with the formation of pyrobitumen.<ref name=ch11r34>Tissot, B. P., D. H. Welte, 1984, Petroleum Formation and Occurrence, 2 ed.: New York, Springer-Verlag, 699 p. 460–461</ref> | | * Gasification of oil in reservoirs is associated with the formation of pyrobitumen.<ref name=ch11r34>Tissot, B. P., D. H. Welte, 1984, Petroleum Formation and Occurrence, 2 ed.: New York, Springer-Verlag, 699 p. 460–461</ref> |
| * Displacement of oil from a trap by gas is associated with asphaltene precipitates and/or relatively unaltered oil stain. | | * Displacement of oil from a trap by gas is associated with asphaltene precipitates and/or relatively unaltered oil stain. |
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| ==Predicting gas destruction== | | ==Predicting gas destruction== |
− | It is not the destruction of methane as much as the lack of economic [[accumulation]]s which occurs at higher maturation levels. Methane occurs in fluid inclusions from lower crustal depths, and shows of methane are not unusual where drilling through low-grade metamorphic rocks—even those at a grade high enough to contain graphite instead of kerogen (R<sub>0</sub> > 8%). For example the Shell Barret #1 well in Hill County, Texas, had a 30-minute methane flare at over [[depth::13,000 ft]] depth in rock described as dolomite and calcite marble with graphitic inclusions.<ref name=ch11r30>Rozendal, R., A., Erskine, W., S., 1971, [http://archives.datapages.com/data/bulletns/1971-73/data/pg/0055/0011/2000/2008.htm Deep test in Ouachita structural belt of Central Texas]: AAPG Bulletin, vol. 56, p. 2008–2017.</ref> | + | It is not the destruction of methane as much as the lack of economic [[accumulation]]s which occurs at higher maturation levels. Methane occurs in fluid inclusions from lower crustal depths, and shows of methane are not unusual where drilling through low-grade metamorphic rocks—even those at a grade high enough to contain graphite instead of [[kerogen]] (R<sub>0</sub> > 8%). For example the Shell Barret #1 well in Hill County, Texas, had a 30-minute methane flare at over [[depth::13,000 ft]] depth in rock described as [[dolomite]] and calcite marble with graphitic inclusions.<ref name=ch11r30>Rozendal, R. A., and W. S. Erskine, 1971, [http://archives.datapages.com/data/bulletns/1971-73/data/pg/0055/0011/2000/2008.htm Deep test in Ouachita structural belt of Central Texas]: AAPG Bulletin, vol. 56, p. 2008–2017.</ref> |
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| The following characteristics can help us predict and recognize gas destruction: | | The following characteristics can help us predict and recognize gas destruction: |
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| * Economic gas [[accumulation]]s become more unusual with maturation levels > 2.8% R<sub>o</sub>.<ref name=ch11r3>Bartenstein, H., 1980, Coalification in NW Germany: Erdöl und Kohle-Erdgas-Petrochemie: vol. 33, p. 121–125.</ref> This is the traditional base of the gas preservation zone. | | * Economic gas [[accumulation]]s become more unusual with maturation levels > 2.8% R<sub>o</sub>.<ref name=ch11r3>Bartenstein, H., 1980, Coalification in NW Germany: Erdöl und Kohle-Erdgas-Petrochemie: vol. 33, p. 121–125.</ref> This is the traditional base of the gas preservation zone. |
− | * The major gas accumulation with the highest well-documented maturity level where [[Calculating charge volume|charging]] occurred before or during exposure to the high temperatures occurs at a maturation level 3.5–3.8% R<sub>o</sub> equivalent (Wilburton field, Oklahoma).<ref name=ch11r13>Hendrick, S., J., 1992, Vitrinite reflectance and deep Arbuckle maturation at Wilburton field, Latimer County, OK: Oklahoma Geological Survey Circular 93, p. 176–184.</ref> | + | * The major gas accumulation with the highest well-documented maturity level where [[Calculating charge volume|charging]] occurred before or during exposure to the high temperatures occurs at a maturation level 3.5–3.8% R<sub>o</sub> equivalent (Wilburton field, Oklahoma).<ref name=ch11r13>Hendrick, S. J., 1992, Vitrinite reflectance and deep Arbuckle maturation at Wilburton field, Latimer County, OK: Oklahoma Geological Survey Circular 93, p. 176–184.</ref> |
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| ==Gas dilution== | | ==Gas dilution== |
| Carbon dioxide, hydrogen sulfide, and nitrogen can constitute a significant percentage of natural gas from some [[accumulation]]s. In some cases, natural gas is uneconomic due to the high nonhydrocarbon gas content. | | Carbon dioxide, hydrogen sulfide, and nitrogen can constitute a significant percentage of natural gas from some [[accumulation]]s. In some cases, natural gas is uneconomic due to the high nonhydrocarbon gas content. |
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− | Although low concentrations of carbon dioxide can be derived from organic sources or byproducts of silicate reactions at moderate temperatures<ref name=ch11r32>Smith, J., T., Ehrenberg, S., N., 1989, Correlation of carbon dioxide abundance with temperature in clastic hydrocarbon reservoirs: relationship to inorganic chemical equilibrium: Marine and Petroleum Geology, vol. 6, p. 129–135., 10., 1016/0264-8172(89)90016-0</ref> high concentrations of carbon dioxide are usually associated with igneous intrusion or regional heating of impure limestones.<ref name=ch11r9>Farmer, R., E., 1965, [http://archives.datapages.com/data/specpubs/methodo2/data/a071/a071/0001/0350/0378.htm Genesis of subsurface carbon dioxide], in Young, A., Galley, J., eds., Fluids in Subsurface Environments: AAPG Memoir No. 4, p. 378–385.</ref> | + | Although low concentrations of carbon dioxide can be derived from organic sources or byproducts of silicate reactions at moderate temperatures<ref name=ch11r32>Smith, J. T., and S. N. Ehrenberg, 1989, Correlation of carbon dioxide abundance with temperature in clastic hydrocarbon reservoirs: relationship to inorganic chemical equilibrium: Marine and Petroleum Geology, vol. 6, p. 129–135., 10., 1016/0264-8172(89)90016-0</ref> high concentrations of carbon dioxide are usually associated with [[igneous]] intrusion or regional heating of impure limestones.<ref name=ch11r9>Farmer, R. E., 1965, [http://archives.datapages.com/data/specpubs/methodo2/data/a071/a071/0001/0350/0378.htm Genesis of subsurface carbon dioxide], in A. Young, and J. Galley, eds., Fluids in Subsurface Environments: AAPG Memoir No. 4, p. 378–385.</ref> |
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− | Hydrogen sulfide concentration increases with depth in gas reservoirs with anhydrite, indicating that it, too, is a product of higher maturity.<ref name=ch11r20 /> The methane is reacting with the sulfate to form hydrogen sulfide and carbon dioxide gas. The reaction is probably kinetically controlled. | + | Hydrogen sulfide concentration increases with depth in gas reservoirs with [[anhydrite]], indicating that it, too, is a product of higher maturity.<ref name=ch11r20 /> The methane is reacting with the sulfate to form hydrogen sulfide and carbon dioxide gas. The reaction is probably kinetically controlled. |
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− | The origin of nitrogen gas is not well characterized. In nonpetroleum basins, nitrogen may have high concentration because no other gas is present to dilute it. High-nitrogen gas in thermally mature basins is possibly from [[coal]] sources<ref name=ch11r33>Stahl, W., Boigk, H., Wollanke, G., 1978, Carbon and nitrogen isotope data of upper Carboniferous and Rotliegend natural gases from north Germany and their relationship to the maturity of the organic source material: Advances in Organic Geochemistry 1976, p. 539–559.</ref> or from the mantle or deep crust.<ref name=ch11r17>Jenden, P., D., Kaplan, I., R., 1989, [http://archives.datapages.com/data/bulletns/1988-89/data/pg/0073/0004/0400/0431.htm Origin of natural gas in Sacramento basin, California]: AAPG Bulletin, vol. 73, p. 431–453.</ref> | + | The origin of nitrogen gas is not well characterized. In nonpetroleum basins, nitrogen may have high concentration because no other gas is present to dilute it. High-nitrogen gas in thermally mature basins is possibly from [[coal]] sources<ref name=ch11r33>Stahl, W., H. Boigk, and G. Wollanke, 1978, Carbon and nitrogen isotope data of upper Carboniferous and Rotliegend natural gases from north Germany and their relationship to the maturity of the organic source material: Advances in Organic Geochemistry 1976, p. 539–559.</ref> or from the [[mantle]] or deep [[crust]].<ref name=ch11r17> Jenden, P. D.,and I. R. Kaplan, 1989, [http://archives.datapages.com/data/bulletns/1988-89/data/pg/0073/0004/0400/0431.htm Origin of natural gas in Sacramento basin, California]: AAPG Bulletin, vol. 73, p. 431–453.</ref> |
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| ==Predicting burial destruction== | | ==Predicting burial destruction== |
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| * Analyzing geohistory or mapping maturation indicators can identify reservoir maturation levels where methane [[accumulation]]s may be uneconomic. Most sizable gas accumulations occurring at maturation levels > 2.8% R<sub>o</sub> have thick claystone seals that help preserve the accumulation. | | * Analyzing geohistory or mapping maturation indicators can identify reservoir maturation levels where methane [[accumulation]]s may be uneconomic. Most sizable gas accumulations occurring at maturation levels > 2.8% R<sub>o</sub> have thick claystone seals that help preserve the accumulation. |
| * Presence of intrusives in the fetch area can indicate a potential for carbon dioxide dilution.<ref name=ch11r29>Parker, C., 1974, Geopressures and secondary porosity in the deep Jurassic of Mississippi: Transactions of the Gulf Coast Association of Geological Societies, vol. 24, p. 69–80.</ref> | | * Presence of intrusives in the fetch area can indicate a potential for carbon dioxide dilution.<ref name=ch11r29>Parker, C., 1974, Geopressures and secondary porosity in the deep Jurassic of Mississippi: Transactions of the Gulf Coast Association of Geological Societies, vol. 24, p. 69–80.</ref> |
− | * If reservoir rocks are associated with evaporite cements or beds, expect hydrogen sulfide if the reservoir is exposed to temperatures > [[temperature::150°C]] and iron is not present to remove the hydrogen sulfide. | + | * If reservoir rocks are associated with [[evaporite]] cements or beds, expect hydrogen sulfide if the reservoir is exposed to temperatures > [[temperature::150°C]] and iron is not present to remove the hydrogen sulfide. |
− | * Nitrogen is released during the late stages of coal maturation.<ref name=ch11r18>Jüntgen, V., H., Karweil, J., 1966, Gasbildung and gasspeicherung in steinkohlenfluzen, I. gasbildung: Erdöl und Kohle-Erdgas-Petrochemie, vol. 19, p. 339–344.</ref> Therefore, if a prospect is [[Calculating charge volume|charged]] by a type III source rock only during its late maturation stage (R<sub>o</sub> > 2.5%), nitrogen dilution is possible. High nitrogen gas content is also characteristic of evaporative settings and hydrocarbon-poor basins. | + | * Nitrogen is released during the late stages of coal maturation.<ref name=ch11r18>Jüntgen, V. H., and J. Karweil, 1966, Gasbildung and gasspeicherung in steinkohlenfluzen, I. gasbildung: Erdöl und Kohle-Erdgas-Petrochemie, vol. 19, p. 339–344.</ref> Therefore, if a prospect is [[Calculating charge volume|charged]] by a type III source rock only during its late maturation stage (R<sub>o</sub> > 2.5%), nitrogen dilution is possible. High nitrogen gas content is also characteristic of evaporative settings and hydrocarbon-poor basins. |
| * Nonhydrocarbon gas concentrations in mature basins can be estimated from evaluating regional gas concentration trends. | | * Nonhydrocarbon gas concentrations in mature basins can be estimated from evaluating regional gas concentration trends. |
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| [[Category:Predicting the occurrence of oil and gas traps]] | | [[Category:Predicting the occurrence of oil and gas traps]] |
| [[Category:Predicting preservation and destruction of accumulations]] | | [[Category:Predicting preservation and destruction of accumulations]] |
| + | [[Category:Treatise Handbook 3]] |