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Origin of Hydrocarbons
Two theories of origin
Inorganic theories
Deep seated
Extra-terrestrial
Organic theory
Evidences
Solid petroleum bitumen occurrence in
igneous environments
Micro-inclusions of petroleum hydrocarbons
have been identified in the minerals of
alkaline igneous rocks.
Association of HC with Hydrothermal systems
Bitumens in several active volcanoes(etna
etc)
Some of the oilfields location (Indonesia,
Mexico)
Extraterrestrial Hypothesis
W. Sokolof proposed a cosmic origin.
It was precipitated as rain from the
original nebular matter from which
the solar system was formed.
Subsequently it was ejected from the
earths interior into the surface rocks
Evidences
The present and the past atmosphere
of the Earth.
Critical discovery of (carbonaceous
chondrite) meteorite
The presence of hydrocarbons on
other planets.
Evidences
Organic origin
Organic origin
Similar to the materials essential for life such
as Proteins, fats and fatty acids.
Fossils led to the anologies with marine life
Whale oil and fish oil
Further similarities with coal
Close association between oil and sediments
Biomarkers- compounds of undoubted organic
derivation. (waxes, porphyrins and steranes)
Carbon isotope C13 and C12
Accumulation of Organic
matter
10,000 of these bugs
would fit on a pinhead!
Plant plankton
en.wikipedia.org/wiki/Image:Ceratium_hirundinella.jpg
Animal plankton
Accumulation of Organic
matter
Today, most plankton can be
found where deep ocean
currents rise to the surface
This upwelling water is rich in
nutrients and causes the
plankton to bloom
Blooms of certain plankton
called dinoflagellates may
give the water a red tinge
Miriam Godfrey
Dinoflagellate bloom
Accumulation of Organic
matter
The renewal of fresh nutrient rich
water doesnot take place.
The water become layered
The deposition takes place below the
thermocline
Accumulation of Organic
matter
en.wikipedia.org/wiki/Image:Nerr0328.jpg
Accumulation of Organic
matter
Source Rocks
Source Rocks
Shale and Limestones
Two major divisions in lithology
A sandwiched layer of organic matter
in between the layers of sediments.
Kerogen
Organic carbon (Weight
percent)
Quality
0.0.5
Poor
0.5-1
Fair
1-2
Good
2-4
Very good
Above 4
Excellent
Kerogen
The TOC may reach 20 percent or
more by weight.
It is highest in coals and rich oil
shales.
The TOC has two parts:
Soluble in organic solvents is
bituminous(bitumen)
Insoluble, nonextractable residue from
the initial transformation of OM is
Kerogen
Kerogen
Carbonates and shales contain
organic matter.
Carbonates contain much less OM
than do shales.
But the OM of the carbonates is
much richer in HC than that of shales
Peters, 1986
TYPES OF KEROGEN
Type I
This type of kerogen is characterized by having a high initial
hydrogen to carbon atomic ratio (H/C) of 1.5 or more, and a
low oxygen to carbon atomic ratio (O/C) of less than 0.1.
Type I kerogen has a hydrogen index greater than 300 and an
oxygen index less than 50.
Its primary source is from algal sediments, such as lacustrine
deposits.
Type I kerogen is also called alginite kerogen, containing high
concentrations of alkanes and fatty acids.
It is the best source for oil-prone maturation, but unfortunately
it is very rare.
Type II
This type of kerogen has a relatively high H/C ratio (1.0 to 1.4)
and a low O/C ratio (0.09 to 1.5).
Type II kerogen has a hydrogen index between 200 and 300,
and an oxygen index between 50 and 100.
It consists of abundant moderate length aliphatic chains and
naphthenic rings.
Ester bonds are common and sulfur is present in substantial
amounts.
Type II kerogen is also called exinite, and is usually associated
with marine sediments, where autochthonous organic matter
(bacteria, phytoplankton and zooplankton) have been deposited
in a reducing environment.
It is a good oil or gas prone kerogen. It is more common than
alginite.
Type III
This type of kerogen has a relatively low H/C ratio (usually <1.0)
and low O/C ratio (0.2 to 0.3).
Type III kerogen has a hydrogen index below 300 and an
oxygen index above 100.
It contains an important proportion of polyaromatic nuclei and
heteroatomic ketone and carboxylic acid groups.
Aliphatic groups are a minor constituent, usually consisting of
longer chains originating from higher-order plant waxes.
The main source of this type of kerogen are continental plants
found in thick detrital sedimentation along continental margins.
This type of kerogen is also called vitrinite. It is less favorable for
oil generation, but will provide a source rock for gas.
Productivity
Grain size
Sedimentation rate
Oxidation/Reduction
ENVIRONMENT OF TRANSFORMATION
Mostly Hydrogen and Carbon are needed
Oxygen and Nitrogen should be removed
Conversion of organic
matter
The transformation of OM to kerogen proceeds
from shallow depths of burial to depths of
perhaps 1000m, with temperatures up to 50
degree centgrades.
On further burial and heating, the large
molecules crack to form smaller, lower
molecular weight hydrocarbons
(geomonomers), around 1000-6000 m depth
and 50-175 degree centigrade temperature.
Conversion of organic
matter
Initial products are H2O and CO2
Hydrogen, methane and liquid
products C13 C30.
Oxygen is lost most rapidly by
dehydration and decarboxylation
Carbon and Nitrogen are lost least
rapidly.
Conversion of organic
matter
The progressive alteration of OM
leads to two fractions:
A fluid product high in hydrogen,
eventually petroleum and natural gas.
A residue high in carbon, such as
bituminous coal.
Increase in the atomic ratio of hydrogencarbon in the oils.
Conversion of Kerogen
Organic matter: 1%
Barker, 1996
Kerogen 90%
Bitumen 10%
Precursors of Petroleum
Humic- gas prone
Sapropelic- oil prone
Classification of Humic and
sapropelic on the basis of H:C :
Less than 0.8, predominantly humic.
Between 0.8 and 1.0, mixed
Above 1.0, predominantly sapropelic.
Permeability
Definition
Formula
Procedure
Controlling factors.