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kerogen

 
Dictionary: ker·o·gen   (kĕr'ə-jən) pronunciation
n.
A fossilized material in shale and other sedimentary rock that yields oil upon heating.

[Greek kēros, wax + -GEN.]


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Complex mixture of compounds with large molecules containing mainly hydrogen and carbon but also oxygen, nitrogen, and sulfur. Kerogen is a precursor of petroleum and the organic component of oil shales. It is waxy and insoluble in water; upon heating, it breaks down into recoverable gaseous and liquid substances resembling petroleum. It consists of compacted organic material, such as algae and other low plant forms, pollen, spores and spore coats, and insects.

For more information on kerogen, visit Britannica.com.

The complex, disseminated organic matter present in sedimentary rocks that remains undissolved by sequential treatment with common organic solvents followed by treatment with nonoxidizing mineral hydrochloric acid and hydrofluoric acid. See also Sedimentary rocks.

Kerogen is considered to be the major starting material for most oil and gas generation as sediments are subjected to geothermal heating in the subsurface. It is the most abundant form of organic carbon on Earth—about 1000 times more abundant than coal, which forms primarily from terrigenous remains of higher plants. Kerogen is formed from the remains of marine and lacustrine microorganisms, plants and animals, and variable amounts of terrigenous debris in sediments. The terrestrial portions of kerogen have elemental compositions similar to coal. See also Coal.

Kerogens are classified according to their atomic ratios of hydrogen to carbon (H/C) and oxygen to carbon (O/C), with oil-prone kerogens being generally higher in H/C and lower in O/C than the gas-prone kerogens. With increasing length of exposure to subsurface temperatures, all kerogens show decreases in the O/C and H/C ratios as they generate preferentially carbon dioxide and water, then oil, and finally only gas (methane) at progressively higher subsurface depths and temperatures. See also Natural gas; Petroleum.


Wikipedia: Kerogen
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Kerogen is a mixture of organic chemical compounds that make up a portion of the organic matter in sedimentary rocks.[1] It is insoluble in normal organic solvents because of the huge molecular weight (upwards of 1,000 Daltons) of its component compounds. The soluble portion is known as bitumen. When heated to the right temperatures in the Earth's crust, (oil window ca. 60°-120°C, gas window ca.120°-150°C) some types of kerogen release crude oil or natural gas, collectively known as hydrocarbons (fossil fuels). When such kerogens are present in high concentration in rocks such as shale they form possible source rocks. Shales rich in kerogens that have not been heated to a sufficient temperature to release their hydrocarbons may form oil shale deposits.

The name "kerogen" was introduced by the Scottish organic chemist Alexander Crum Brown in 1912.[2][3]

Contents

Composition

As kerogen is a mixture of organic material, rather than a specific chemical; it cannot be given a chemical formula. Indeed its chemical composition can vary distinctively from sample to sample. Kerogen from the Green River Formation oil shale deposit of western North America contains elements in the proportions C 215 : H 330 : O 12 : N 5 : S 1.[2]

Types

Labile kerogen breaks down to form heavy hydrocarbons (i.e. oils), refractory kerogen breaks down to form light hydrocarbons (i.e. gases), and inert kerogen forms graphite.

A Van Krevelen diagram is one example of classifying kerogens, where they tend to form groups when the ratios of hydrogen to carbon and oxygen to carbon are compared.[4]

Type I

Type II

  • Hydrogen:Carbon ratio < 1.25
  • Oxygen:Carbon ratio 0.03 to 0.18
  • Tend to produce a mix of gas and oil.
  • Several types: exinite, cutinite, resinite, and liptinite
    • Exinite: formed from the casings of pollen and spores
    • Cutinite: formed from terrestrial plant cuticle
    • Resinite: formed from terrestrial plant resins and animal decomposition resins
    • Liptinite: formed from terrestrial plant lipids (hydrophobic molecules that are soluble in organic solvents) and marine algae

They all have great tendencies to produce petroleum and are all formed from lipids deposited under reducing conditions.

Type II-Sulfur

  • Similar to Type II but high in sulfur.

Type III

  • Hydrogen:Carbon ratio < 1
  • Oxygen:Carbon ratio 0.03 to 0.3
  • Material is thick, resembling wood or coal.
  • Tends to produce coal and gas (Recent research has shown that type III kerogens can actually produce oil under extreme conditions) <ref: Krause FF, 2009>
  • Has very low hydrogen because of the extensive ring and aromatic systems

Kerogen Type III is formed from terrestrial plant matter that is lacking in lipids or waxy matter. It forms from cellulose, the carbohydrate polymer that forms the rigid structure of terrestrial plants, lignin, a non-carbohydrate polymer formed from phenyl-propane units that binds the strings of cellulose together, and terpenes and phenolic compounds in the plant.

Most of the biomass that eventually becomes petroleum is contributed by the bacteria and protists that decompose the primary matter, not the primary matter itself. However, the lignin in this kerogen decomposes to form phenolic compounds that are toxic to bacteria and protists. Without this extra input, it will only become methane and/or coal.

Type IV (residue)

  • Hydrogen:Carbon < 0.5

Type IV kerogen contains mostly decomposed organic matter in the form of polycyclic aromatic hydrocarbons. They have no potential to produce hydrocarbons.

Origin of material

Terrestrial material

The type of material is difficult to determine but several apparent patterns have been noticed.

  • Ocean or lake material often meet kerogen type III or IV classifications.
  • Ocean or lake material deposited under anoxic conditions often form kerogens of type I or II.
  • Most higher land plants produce kerogens of type III or IV.
  • Some coal contains type II kerogen.

Extraterrestrial material

See also

References

  1. ^ Oilfield Glossary
  2. ^ a b Teh Fu Yen; Chilingar, George V. (1976). Oil Shale. Amsterdam: Elsevier. pp. 27. ISBN 9780444414083. http://books.google.com/books?id=qkU7OcVkwaIC&pg=PA27. Retrieved on 2009-05-31. 
  3. ^ Hutton, Adrian C.; Bharati, Sunil; Robl, Thomas (1994). "Chemical and Petrographic Classification of Kerogen/Macerals". Energy Fuels (Elsevier Science) 8 (6): 1478–1488. doi:10.1021/ef00048a038. 
  4. ^ Example of a Van Krevelen diagram
  5. ^ Nakamura, T. (2005) Post-hydration thermal metamorphism of carbonaceous chondrites, Journal of Mineralogical and Petrological Sciences, volume 100, page 268, [1] (PDF) Retrieved 1 September 2007
  6. ^ Papoular, R. (2001) The use of kerogen data in understanding the properties and evolution of interstellar carbonaceous dust, Astronomy and Astrophysics, volume 378, pages 597-607, [2] (PDF) Retrieved 1 September 2007

External links


 
 
Learn More
oil shale (geology)
Organic geochemistry (geochemistry)
Coal (mineralogy and petrology)

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