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Showing posts with label petroleum. Show all posts
Showing posts with label petroleum. Show all posts

Friday, 23 December 2016

Reservoir Rocks

 
Reservoir Rocks


Reservoir Rocks:

“The rock, which is porous and permeable, contains oil and gas becomes a reservoir rock.” OR
“Permeable subsurface rock that contains petroleum”
It can be different from source rock with respect to grain size and pore spaces.
Nearly all rocks are reservoir and can be classified accordingly as
·         Clastic Rocks
·         Carbonate Rocks
·         Igneous/Metamorphic Rocks

Clastic Rocks

Aggregates of a particle, fragments of older rocks
Range in size from fine clay to boulder size forming various clastic rocks, including claystone, shale, siltstone, sandstone, conglomerates.
Most important reservoir rocks in this category are sandstone and sometimes conglomerate due to porosity and permeability. The fractured shale reservoir is also possible but uncommon in nature.

Carbonate Rocks

Formed by chemical precipitation or biological precipitation.
The most important reservoir in this category are limestone and dolomite.

Igneous/Metamorphic Rocks

These are rare comparatively to clastic and carbonate reservoir rocks, from which commercial oil and gas are produced.
e.g., there are number of volcanic oil fields, which contains oil and gas includes: Columbia Plateaue of Washington and Oregon, the Mexico-Arizona Volcanic field, the Deccan Traps of India and volcanic of pacific.

Reservoir Rocks Properties:

There are two main properties on the basis of which reservoir quality of rocks is controlled.
·         Porosity
·         Permeability

Porosity:

“It is the ratio of pore spaces volume to the total volume (bulk volume) of a reservoir rock.”
It is expressed in %age.
Mathematically: Porosity = Pore volume/Bulk volume x 100

Porosity on the basis of origin

·         Primary Porosity
·         Secondary Porosity

Primary Porosity:

Porosity which developed at time of deposition.
Depends upon; size, shape and pattern of arrangement of grains
e.g., uniform grain size higher the porosity, perfectly rounded shape higher the porosity. In last when packing is cubic of same size grain higher the porosity (47.6%) rather than rhombohedral grains (25.9%).

Secondary Porosity:

Porosity which is developed after the sedimentation process due to physical and chemical effects.
The physical and chemical effects includes
·         Compaction
·         Fracturing
·         Dissolution
·         Cementation
·         Recrystallization
·         Dolomitization
Porosity based on the pore space connectivity Both primary and secondary porosity could be:
·         Absolute Porosity
·         Effective Porosity

Absolute Porosity:

The ratio of total volume of pore spaces to  total volume of rock

Effective Porosity

The ratio of the volume of interconnected pore spaces to the total volume of the rock.
 There are four basic porosity types within sandstone (after, Pittman, 1979)
·         Intragranular Porosity
·         Intergranular Porosity
·       Dissolution porosity

·    Fractured Porosity

Porosity in Carbonates (Limestone):

 There are many types of porosities within limestone but can be groups together in three groups (after Choquette and Pray, 1970) such as:

1. fabric selective
2.non fabric selective
3.fabric selective or Not





Porosity in Igneous/Metamorphic Rocks:

There might be only a fracture porosity. 

Permeability:

“Ability of a rock to permit fluidflow” through the inter-conneted pores.
 It is expressed by m2. Mathematically it can be written as by Darcy’s law:
q/A= KAP/p AL
q= volumetric flow rates, m3/s A= cross sectional area, m2 K= permeability, m2
AP/AL= pressure gradient in direction of flow, Pa/m p= viscosity, Pa.s

Types of Permeability

Ø  Absolute Permeability
When only one fluid saturate the effective pore spaces and can pass through effective pores.
Effective Permeability
When only one fluid can pass through effective pores in presence of other fluid.
Ø  Relative Permeability
The ratio of effective permeability to the absolute permeability

Geochemical Fossils and Their Significance in Petroleum Formation

 
Geochemical Fossils and Their Significance in Petroleum Formation


Geochemical Fossils and Their Significance in Petroleum Formation

“saturated hydrocarbons having branching chain structure produced by certain organism action”
These come from plant and animals: these are helpful in locating the source on the basis of structure
High molecular having formula: Cn H2n-x: ratio between C:H<2
There are various types of geochemical fossils
Long Chain Paraffin
Complex Ring Alcohols
Triterpentinoid Alcohols
Acyclic Isoprenoids
1. Long Chain Paraffin  Derived from waxes of higher plants

2.Complex Ring Alcohols

Based on cyclohexane and are derived from plants and animals

3.Triterpentinoid Alcohols

These are aromatic compounds based on terpene
Terpene: organic compound having basic structure (C10 H16) or Multiple of (C10 H16) e.g. Steroid having formula (C30 H50 OH) as an alcohol of terpene

4.Acyclic Isoprenoids

Compounds based on isoprene: chemical composition is (C6 H8)
Compounds may have multiple of isoprene
Isoprenoid: formed long branched and saturated molecule, branching is every 4th cation of isoprene having methyl group
Occurs in sediments with abundance derivatives from chlorophyl from plants and hemin form animals

Significance

They are useful indicators of oil origin
Typical example are Pristane and Phytene
Pristane: 2,6,10,14 Tetra methyl pentadecane, it has nineteen carbon in
skeleon
Phytene: Tetra methyl hexadecane, it has twenty carbon in its skeleton
 Ratio of Pristane and Phytene (Pristane:Phytene)
ratio measured chromatographically from oil or rock sample, it indicates the organic matter from which oil is originated or thermal maturation of source.
High ratio indicates large contribution form teristrial OM
The ratio is therefore a vital “finger prints” for any crude oil, containing both molecule.
Finger prints: because it has to identify the source of OM

Catagenesis

Principle Stage of oil formation

T continue to increase, bonds break down e.g., ester and some C-C bonds
H/Cs molecules, and particularly aliphatic chains, are produced from kerogen and from previously generated N, S, O compounds
Some H/Cs are C15-C30, which are comparable to geochemical fossils, entrapped in kerogen or linked by ester bonding.
However, most of new molecule has medium to low molecular weight
This is priciple zone of oil formation, as described by Vassoevich, 1969, however, also some significant amount of gas.

Principle Stage of Condensate and Wet Gas Formation

P-T continues to increase, breaking of C-C bonds occur more frequently
Light hydrocarbons are generated through cracking from remaining kerogen and in petroleum; the quickly dominated compound is methane.
Overall transformation is equivalent to disproportionation;
On one hand H/Cs increasing in Hydrogen content are genereated having average atomic ratio H/C is 1.5 to 2.0 in crude oil and 4.0 in methatne
 On the other hand, the residue kerogen depleted in hydrogen H/C of about 0.5 by the end of catagenesis.
Metagenesis: Dry gas Zone
After most liable material has been eliminated through catagenesis, however, in this stage no significance amounts of H/Cs are generated except some methane
Which may result from cracking of source rock H/Cs and reserviored liquid petroleum

Physiochemical Changes or Transformation of Organic Matter to Petroleum

 
Physiochemical Changes or Transformation of Organic Matter to Petroleum

Physiochemical Changes or Transformation of Organic Matter to Petroleum 
                                                                                                                      
Sedimentary Deposits, contains: (1) Interstitial water, (2) Organic Matter, (3) Microbial Organism and (4) Dissolved Oxygen
O.M unstable, in order to be in equilibrium reacts with O2 (along with other reactions), here, the physiochemical transformation starts.
This transformation cannot be isolated from initial condition of deposition environment to PT condition.

                                                 Stages/Process of Formation of Petroleum

Main stages are; (1) Diagenesis, (2) Catagenesis and (3) Metagenesis

Diagenesis

“Set of physiochemical changes which takes place at shallow depth after deposition”
OR
“Diagenesis is a process through which the system tends to approach equilibrium under condition of shallow burial and through which the sediments normally becomes consolidated”
e.g., porosity reduction in clay (80% to 60%)
Depth: 200m rarely up to 2000m
No significance change in pressure and temperature (no significance)
At such depths transformation is due to biological activity, carried by bacteria (aerobic or anaerobic)
The energy within system, comes through decomposition, which produces CO2, NH3 and H2O; in sand decomposition is quick rather than mud
Eh of interstitial H2O decreased, Eh= Oxidation/Redcution, PH of system would be increased
OM like Protein, Carbohydrates are soluble in water, severely transformed (more or less completely deformed), which form a compound “Polycondensed Organic Compound or geopolymer”. A geopolymer is an organic compound, which is precursor of Kerogen (if plant materia greater, then first step would be peat then bitumen).
V.R: 0.5
Humic acid produced
During close, humic acid are minimum

Catagenesis

The second stage
T: 50-150/200C, P: 300-1000 bars and rarely 1500 bars, which results in new changes
Composition, texture of mineral phase are consumed, mostly in clay fraction, e.g., water expelled, decreased the porosity and increase in salanity
OM progressively changes:
Kerogen produces:
first liquid petroleum
Wet gas (later stage)
Condensate (later stage)
Both oil and gas are associated with amounts of methane
Massive organic deposits; various rank of coal, with methane.
End of Catagenesis:
Dissappearence of aliphatic carbon chain
V.R: 2.0 (beginning of anthracite rank coal)
Further no more generation of petroleum and minor amount of methane (this point is known as natural break)

Metagenesis

The last stage, in evolution of sediments
H and T High (OM may be exposed to magma or hydrothermal effect)
Mineral severly transformed
Early metagenesis:
Only methane produced
Coal is anthracite
Late metagenesis:
Residue of Carbon
Meta anthracite, graphite schist etc.

Factor Effecting Transformation of OM into Petroleum

Starts within reducing environment, transformation requires energy and are:
Ø  Temperature and Pressure
Ø  Bacterial Activity
Ø  Catalytic Reaction
Ø  Radioactive bombardment

(1)Temperature and Pressure

T combined with P or Low T replaced with Time along with pressure
Kerogen shales: 350-400C to convert into petroleum, presence of porphyrines, indicates T never exceeds than 200C (means time is replacing Temp., enough time would be required)
By laboratory experiments it suggested that Less T required within earth than lab.

(2)Bacterial Activity

Decomposition of OM: Methane produced, through process fermentation
Bacteria produce methane, considered as agency in the formation of other petroleum Hydrocarbons.
Types of Bacteria
Aerobic: requires free O2
Anaerobic: requires combine O2
Faculative: live in presence or absence of O2, can be found in well and helps in , extent unknown.

(3)Catalytic Reaction

 Takes no part in reaction but only accelerates it: same in composition at beginning and at the end.
 May promote the conversion of Kerogen to petroleum at low temperature.
Similarly, Ni, Mo and V like catalysts are also found in Ash/residue from the Petroleum.

(4)Radioactive Bombardment

Heat from radioactive bombardment is also possible source of energy.
Important: uranium, thorium and potassium.
e.g., fatty acid----(alpha)----paraffin hydrocarbon
cyclohexane carboxylic acid----(alpha)-----cyclohexane

Early Transformation of OM: The Diagenetic Pathway from Organisms to Geochemical Fossil and Kerogen            (Source Rock)

OM, subjected to various degree of microbial and chemical actions: as a result its composition largely changed (during sedimentation process or after sedimentation within young sediments)
By comparison, 20% of OM recoverable, rest is lost; due to degradation in nutrients, then polycondensation to form kerogen at the end
Kerogen is the main source of petroleum (by geochemists)
The whole process is known as or referred to as diagenesis: leads to biopolymers synthesized by living organisms to geopolymers (Kerogen) through fractionation.
> Diagensis: the partial destruction and rearrangement of building stones.
Diagensis can be further divided into:
Biochemical Degradation
Polycondensation
Insolubilization

1 Biochemical Degradation

As we know there are four constituents of recent sediment deposited as source of OM (i. water, ii. organic matter, iii. minerals, iv. microbial organisms: shallow depths)
> Biochemical degradation is divided into:

a). Microbial Activity:

Bacteria + Fungi; present in variety of places (water, soil and in sed).
They would decomposed OM: build up their cells: aerobic and anaerobic (with and without O2).
OM compound dissolve through enzymatic process by organism; then take for their synthesis in their molecule.
Protein + Carbohydrate          (hydrolysed)    Amino Acid +
Surgars
Lipid + Lignins           less active
> In oxidizing; all OM destroyed
In fine grain sediments:
Dissolve oxygen used in pore spaces
Established anaerobic condition: under which, OM—partly decomposed by fermentation (in which sulphates reduced to S, Iron to Fe)
Fermentation: oxidized form of OM e.g., Cellulose   Methane + CO2

b) Free or Hydrolyzable Organic Matter

Sugar and protein: degraded can be found in addition to fatty acid + H/C (Methane): this amount is quite low
About 75-90% OM not destroyed and called as “humin” or “humic acid”
> Up to certain level most of the hydrolysable and free compounds disappeared.

2 Polycondensation

Remaining “humic acid” (residue left from micro-organism) incorporated into new polymeric insoluble structures (humic compounds)
Humic acid; results from the polycondensation of Organic residue of microbial metabolism (more or less oxidizing condition)
Oxidative condensation of Phenol is important process: addition of nitrogenous compound--- occur---through random polymerization-- -of free radicle like semiquinone
Soil humic acid structure (swaim, 1963): polycondensates made of nuclei bearing reactive groups; connected by bridges
a) nuclei: simple/or condensed aromatic/naphtenic
b) bridges: oxygen, sulphur, peptide or methylene bonds
Important reactive group is OH

3 Insolubilization

Decomposition + Polycondensation: first few meters of sediments; which represents 90% of total organic matter in young sediments
With increase in depth fulvic + humic acid converted into humin (insoluble)
Insolubilization occurs during diagenesis on a wider scale w.r.t time and depth (greater time and greater depth w.r.t other two steps)


Early Transformation of OM: The Diagenetic Pathway from Organisms to Geochemical Fossil and Kerogen            (Source Rock)

OM, subjected to various degree of microbial and chemical actions: as a result its composition largely changed (during sedimentation process or after sedimentation within young sediments)
By comparison, 20% of OM recoverable, rest is lost; due to degradation in nutrients, then polycondensation to form kerogen at the end
Kerogen is the main source of petroleum (by geochemists)
The whole process is known as or referred to as diagenesis: leads to biopolymers synthesized by living organisms to geopolymers (Kerogen) through fractionation.
> Diagensis: the partial destruction and rearrangement of building stones.
Diagensis can be further divided into:
Biochemical Degradation
Polycondensation
Insolubilization

1 Biochemical Degradation

As we know there are four constituents of recent sediment deposited as source of OM (i. water, ii. organic matter, iii. minerals, iv. microbial organisms: shallow depths)
> Biochemical degradation is divided into:

a). Microbial Activity:

Bacteria + Fungi; present in variety of places (water, soil and in sed).
They would decomposed OM: build up their cells: aerobic and anaerobic (with and without O2).
OM compound dissolve through enzymatic process by organism; then take for their synthesis in their molecule.
Protein + Carbohydrate          (hydrolysed)    Amino Acid +
Surgars
Lipid + Lignins           less active
> In oxidizing; all OM destroyed
In fine grain sediments:
Dissolve oxygen used in pore spaces
Established anaerobic condition: under which, OM—partly decomposed by fermentation (in which sulphates reduced to S, Iron to Fe)
Fermentation: oxidized form of OM e.g., Cellulose   Methane + CO2

b) Free or Hydrolyzable Organic Matter

Sugar and protein: degraded can be found in addition to fatty acid + H/C (Methane): this amount is quite low
About 75-90% OM not destroyed and called as “humin” or “humic acid”
> Up to certain level most of the hydrolysable and free compounds disappeared.

2 Polycondensation

Remaining “humic acid” (residue left from micro-organism) incorporated into new polymeric insoluble structures (humic compounds)
Humic acid; results from the polycondensation of Organic residue of microbial metabolism (more or less oxidizing condition)
Oxidative condensation of Phenol is important process: addition of nitrogenous compound--- occur---through random polymerization-- -of free radicle like semiquinone
Soil humic acid structure (swaim, 1963): polycondensates made of nuclei bearing reactive groups; connected by bridges
a) nuclei: simple/or condensed aromatic/naphtenic
b) bridges: oxygen, sulphur, peptide or methylene bonds
Important reactive group is OH

3 Insolubilization

Decomposition + Polycondensation: first few meters of sediments; which represents 90% of total organic matter in young sediments
With increase in depth fulvic + humic acid converted into humin (insoluble)
Insolubilization occurs during diagenesis on a wider scale w.r.t time and depth (greater time and greater depth w.r.t other two steps)

Early Transformation of OM: The Diagenetic Pathway from Organisms to Geochemical Fossil and Kerogen            (Source Rock)

OM, subjected to various degree of microbial and chemical actions: as a result its composition largely changed (during sedimentation process or after sedimentation within young sediments)
By comparison, 20% of OM recoverable, rest is lost; due to degradation in nutrients, then polycondensation to form kerogen at the end
Kerogen is the main source of petroleum (by geochemists)
The whole process is known as or referred to as diagenesis: leads to biopolymers synthesized by living organisms to geopolymers (Kerogen) through fractionation.
> Diagensis: the partial destruction and rearrangement of building stones.
Diagensis can be further divided into:
Biochemical Degradation
Polycondensation
Insolubilization

1 Biochemical Degradation

As we know there are four constituents of recent sediment deposited as source of OM (i. water, ii. organic matter, iii. minerals, iv. microbial organisms: shallow depths)
> Biochemical degradation is divided into:

a). Microbial Activity:

Bacteria + Fungi; present in variety of places (water, soil and in sed).
They would decomposed OM: build up their cells: aerobic and anaerobic (with and without O2).
OM compound dissolve through enzymatic process by organism; then take for their synthesis in their molecule.
Protein + Carbohydrate          (hydrolysed)    Amino Acid +
Surgars
Lipid + Lignins           less active
> In oxidizing; all OM destroyed
In fine grain sediments:
Dissolve oxygen used in pore spaces
Established anaerobic condition: under which, OM—partly decomposed by fermentation (in which sulphates reduced to S, Iron to Fe)
Fermentation: oxidized form of OM e.g., Cellulose   Methane + CO2

b) Free or Hydrolyzable Organic Matter

Sugar and protein: degraded can be found in addition to fatty acid + H/C (Methane): this amount is quite low
About 75-90% OM not destroyed and called as “humin” or “humic acid”
> Up to certain level most of the hydrolysable and free compounds disappeared.

2 Polycondensation

Remaining “humic acid” (residue left from micro-organism) incorporated into new polymeric insoluble structures (humic compounds)
Humic acid; results from the polycondensation of Organic residue of microbial metabolism (more or less oxidizing condition)
Oxidative condensation of Phenol is important process: addition of nitrogenous compound--- occur---through random polymerization-- -of free radicle like semiquinone
Soil humic acid structure (swaim, 1963): polycondensates made of nuclei bearing reactive groups; connected by bridges
a) nuclei: simple/or condensed aromatic/naphtenic
b) bridges: oxygen, sulphur, peptide or methylene bonds
Important reactive group is OH

3 Insolubilization

Decomposition + Polycondensation: first few meters of sediments; which represents 90% of total organic matter in young sediments
With increase in depth fulvic + humic acid converted into humin (insoluble)
Insolubilization occurs during diagenesis on a wider scale w.r.t time and depth (greater time and greater depth w.r.t other two steps)

Early Transformation of OM: The Diagenetic Pathway from Organisms to Geochemical Fossil and Kerogen            (Source Rock)

OM, subjected to various degree of microbial and chemical actions: as a result its composition largely changed (during sedimentation process or after sedimentation within young sediments)
By comparison, 20% of OM recoverable, rest is lost; due to degradation in nutrients, then polycondensation to form kerogen at the end
Kerogen is the main source of petroleum (by geochemists)
The whole process is known as or referred to as diagenesis: leads to biopolymers synthesized by living organisms to geopolymers (Kerogen) through fractionation.
> Diagensis: the partial destruction and rearrangement of building stones.
Diagensis can be further divided into:
Biochemical Degradation
Polycondensation
Insolubilization

1 Biochemical Degradation

As we know there are four constituents of recent sediment deposited as source of OM (i. water, ii. organic matter, iii. minerals, iv. microbial organisms: shallow depths)
> Biochemical degradation is divided into:

a). Microbial Activity:

Bacteria + Fungi; present in variety of places (water, soil and in sed).
They would decomposed OM: build up their cells: aerobic and anaerobic (with and without O2).
OM compound dissolve through enzymatic process by organism; then take for their synthesis in their molecule.
Protein + Carbohydrate          (hydrolysed)    Amino Acid +
Surgars
Lipid + Lignins           less active
> In oxidizing; all OM destroyed
In fine grain sediments:
Dissolve oxygen used in pore spaces
Established anaerobic condition: under which, OM—partly decomposed by fermentation (in which sulphates reduced to S, Iron to Fe)
Fermentation: oxidized form of OM e.g., Cellulose   Methane + CO2

b) Free or Hydrolyzable Organic Matter

Sugar and protein: degraded can be found in addition to fatty acid + H/C (Methane): this amount is quite low
About 75-90% OM not destroyed and called as “humin” or “humic acid”
> Up to certain level most of the hydrolysable and free compounds disappeared.

2 Polycondensation

Remaining “humic acid” (residue left from micro-organism) incorporated into new polymeric insoluble structures (humic compounds)
Humic acid; results from the polycondensation of Organic residue of microbial metabolism (more or less oxidizing condition)
Oxidative condensation of Phenol is important process: addition of nitrogenous compound--- occur---through random polymerization-- -of free radicle like semiquinone
Soil humic acid structure (swaim, 1963): polycondensates made of nuclei bearing reactive groups; connected by bridges
a) nuclei: simple/or condensed aromatic/naphtenic
b) bridges: oxygen, sulphur, peptide or methylene bonds
Important reactive group is OH

3 Insolubilization

Decomposition + Polycondensation: first few meters of sediments; which represents 90% of total organic matter in young sediments
With increase in depth fulvic + humic acid converted into humin (insoluble)
Insolubilization occurs during diagenesis on a wider scale w.r.t time and depth (greater time and greater depth w.r.t other two steps)

Early Transformation of OM: The Diagenetic Pathway from Organisms to Geochemical Fossil and Kerogen            (Source Rock)

OM, subjected to various degree of microbial and chemical actions: as a result its composition largely changed (during sedimentation process or after sedimentation within young sediments)
By comparison, 20% of OM recoverable, rest is lost; due to degradation in nutrients, then polycondensation to form kerogen at the end
Kerogen is the main source of petroleum (by geochemists)
The whole process is known as or referred to as diagenesis: leads to biopolymers synthesized by living organisms to geopolymers (Kerogen) through fractionation.
> Diagensis: the partial destruction and rearrangement of building stones.
Diagensis can be further divided into:
Biochemical Degradation
Polycondensation
Insolubilization

1 Biochemical Degradation

As we know there are four constituents of recent sediment deposited as source of OM (i. water, ii. organic matter, iii. minerals, iv. microbial organisms: shallow depths)
> Biochemical degradation is divided into:

a). Microbial Activity:

Bacteria + Fungi; present in variety of places (water, soil and in sed).
They would decomposed OM: build up their cells: aerobic and anaerobic (with and without O2).
OM compound dissolve through enzymatic process by organism; then take for their synthesis in their molecule.
Protein + Carbohydrate          (hydrolysed)    Amino Acid +
Surgars
Lipid + Lignins           less active
> In oxidizing; all OM destroyed
In fine grain sediments:
Dissolve oxygen used in pore spaces
Established anaerobic condition: under which, OM—partly decomposed by fermentation (in which sulphates reduced to S, Iron to Fe)
Fermentation: oxidized form of OM e.g., Cellulose   Methane + CO2

b) Free or Hydrolyzable Organic Matter

Sugar and protein: degraded can be found in addition to fatty acid + H/C (Methane): this amount is quite low
About 75-90% OM not destroyed and called as “humin” or “humic acid”
> Up to certain level most of the hydrolysable and free compounds disappeared.

2 Polycondensation

Remaining “humic acid” (residue left from micro-organism) incorporated into new polymeric insoluble structures (humic compounds)
Humic acid; results from the polycondensation of Organic residue of microbial metabolism (more or less oxidizing condition)
Oxidative condensation of Phenol is important process: addition of nitrogenous compound--- occur---through random polymerization-- -of free radicle like semiquinone
Soil humic acid structure (swaim, 1963): polycondensates made of nuclei bearing reactive groups; connected by bridges
a) nuclei: simple/or condensed aromatic/naphtenic
b) bridges: oxygen, sulphur, peptide or methylene bonds
Important reactive group is OH

3 Insolubilization

Decomposition + Polycondensation: first few meters of sediments; which represents 90% of total organic matter in young sediments
With increase in depth fulvic + humic acid converted into humin (insoluble)
Insolubilization occurs during diagenesis on a wider scale w.r.t time and depth (greater time and greater depth w.r.t other two steps)

Early Transformation of OM: The Diagenetic Pathway from Organisms to Geochemical Fossil and Kerogen            (Source Rock)

OM, subjected to various degree of microbial and chemical actions: as a result its composition largely changed (during sedimentation process or after sedimentation within young sediments)
By comparison, 20% of OM recoverable, rest is lost; due to degradation in nutrients, then polycondensation to form kerogen at the end
Kerogen is the main source of petroleum (by geochemists)
The whole process is known as or referred to as diagenesis: leads to biopolymers synthesized by living organisms to geopolymers (Kerogen) through fractionation.
> Diagensis: the partial destruction and rearrangement of building stones.
Diagensis can be further divided into:
Biochemical Degradation
Polycondensation
Insolubilization

1 Biochemical Degradation

As we know there are four constituents of recent sediment deposited as source of OM (i. water, ii. organic matter, iii. minerals, iv. microbial organisms: shallow depths)
> Biochemical degradation is divided into:

a). Microbial Activity:

Bacteria + Fungi; present in variety of places (water, soil and in sed).
They would decomposed OM: build up their cells: aerobic and anaerobic (with and without O2).
OM compound dissolve through enzymatic process by organism; then take for their synthesis in their molecule.
Protein + Carbohydrate          (hydrolysed)    Amino Acid +
Surgars
Lipid + Lignins           less active
> In oxidizing; all OM destroyed
In fine grain sediments:
Dissolve oxygen used in pore spaces
Established anaerobic condition: under which, OM—partly decomposed by fermentation (in which sulphates reduced to S, Iron to Fe)
Fermentation: oxidized form of OM e.g., Cellulose   Methane + CO2

b) Free or Hydrolyzable Organic Matter

Sugar and protein: degraded can be found in addition to fatty acid + H/C (Methane): this amount is quite low
About 75-90% OM not destroyed and called as “humin” or “humic acid”
> Up to certain level most of the hydrolysable and free compounds disappeared.

2 Polycondensation

Remaining “humic acid” (residue left from micro-organism) incorporated into new polymeric insoluble structures (humic compounds)
Humic acid; results from the polycondensation of Organic residue of microbial metabolism (more or less oxidizing condition)
Oxidative condensation of Phenol is important process: addition of nitrogenous compound--- occur---through random polymerization-- -of free radicle like semiquinone
Soil humic acid structure (swaim, 1963): polycondensates made of nuclei bearing reactive groups; connected by bridges
a) nuclei: simple/or condensed aromatic/naphtenic
b) bridges: oxygen, sulphur, peptide or methylene bonds
Important reactive group is OH

3 Insolubilization

Decomposition + Polycondensation: first few meters of sediments; which represents 90% of total organic matter in young sediments
With increase in depth fulvic + humic acid converted into humin (insoluble)
Insolubilization occurs during diagenesis on a wider scale w.r.t time and depth (greater time and greater depth w.r.t other two steps)

Early Transformation of OM: The Diagenetic Pathway from Organisms to Geochemical Fossil and Kerogen            (Source Rock)

OM, subjected to various degree of microbial and chemical actions: as a result its composition largely changed (during sedimentation process or after sedimentation within young sediments)
By comparison, 20% of OM recoverable, rest is lost; due to degradation in nutrients, then polycondensation to form kerogen at the end
Kerogen is the main source of petroleum (by geochemists)
The whole process is known as or referred to as diagenesis: leads to biopolymers synthesized by living organisms to geopolymers (Kerogen) through fractionation.
> Diagensis: the partial destruction and rearrangement of building stones.
Diagensis can be further divided into:
Biochemical Degradation
Polycondensation
Insolubilization

1 Biochemical Degradation

As we know there are four constituents of recent sediment deposited as source of OM (i. water, ii. organic matter, iii. minerals, iv. microbial organisms: shallow depths)
> Biochemical degradation is divided into:

a). Microbial Activity:

Bacteria + Fungi; present in variety of places (water, soil and in sed).
They would decomposed OM: build up their cells: aerobic and anaerobic (with and without O2).
OM compound dissolve through enzymatic process by organism; then take for their synthesis in their molecule.
Protein + Carbohydrate          (hydrolysed)    Amino Acid +
Surgars
Lipid + Lignins           less active
> In oxidizing; all OM destroyed
In fine grain sediments:
Dissolve oxygen used in pore spaces
Established anaerobic condition: under which, OM—partly decomposed by fermentation (in which sulphates reduced to S, Iron to Fe)
Fermentation: oxidized form of OM e.g., Cellulose   Methane + CO2

b) Free or Hydrolyzable Organic Matter

Sugar and protein: degraded can be found in addition to fatty acid + H/C (Methane): this amount is quite low
About 75-90% OM not destroyed and called as “humin” or “humic acid”
> Up to certain level most of the hydrolysable and free compounds disappeared.

2 Polycondensation

Remaining “humic acid” (residue left from micro-organism) incorporated into new polymeric insoluble structures (humic compounds)
Humic acid; results from the polycondensation of Organic residue of microbial metabolism (more or less oxidizing condition)
Oxidative condensation of Phenol is important process: addition of nitrogenous compound--- occur---through random polymerization-- -of free radicle like semiquinone
Soil humic acid structure (swaim, 1963): polycondensates made of nuclei bearing reactive groups; connected by bridges
a) nuclei: simple/or condensed aromatic/naphtenic
b) bridges: oxygen, sulphur, peptide or methylene bonds
Important reactive group is OH

3 Insolubilization

Decomposition + Polycondensation: first few meters of sediments; which represents 90% of total organic matter in young sediments
With increase in depth fulvic + humic acid converted into humin (insoluble)
Insolubilization occurs during diagenesis on a wider scale w.r.t time and depth (greater time and greater depth w.r.t other two steps)

Early Transformation of OM: The Diagenetic Pathway from Organisms to Geochemical Fossil and Kerogen            (Source Rock)

OM, subjected to various degree of microbial and chemical actions: as a result its composition largely changed (during sedimentation process or after sedimentation within young sediments)
By comparison, 20% of OM recoverable, rest is lost; due to degradation in nutrients, then polycondensation to form kerogen at the end
Kerogen is the main source of petroleum (by geochemists)
The whole process is known as or referred to as diagenesis: leads to biopolymers synthesized by living organisms to geopolymers (Kerogen) through fractionation.
> Diagensis: the partial destruction and rearrangement of building stones.
Diagensis can be further divided into:
Biochemical Degradation
Polycondensation
Insolubilization

1 Biochemical Degradation

As we know there are four constituents of recent sediment deposited as source of OM (i. water, ii. organic matter, iii. minerals, iv. microbial organisms: shallow depths)
> Biochemical degradation is divided into:

a). Microbial Activity:

Bacteria + Fungi; present in variety of places (water, soil and in sed).
They would decomposed OM: build up their cells: aerobic and anaerobic (with and without O2).
OM compound dissolve through enzymatic process by organism; then take for their synthesis in their molecule.
Protein + Carbohydrate          (hydrolysed)    Amino Acid +
Surgars
Lipid + Lignins           less active
> In oxidizing; all OM destroyed
In fine grain sediments:
Dissolve oxygen used in pore spaces
Established anaerobic condition: under which, OM—partly decomposed by fermentation (in which sulphates reduced to S, Iron to Fe)
Fermentation: oxidized form of OM e.g., Cellulose   Methane + CO2

b) Free or Hydrolyzable Organic Matter

Sugar and protein: degraded can be found in addition to fatty acid + H/C (Methane): this amount is quite low
About 75-90% OM not destroyed and called as “humin” or “humic acid”
> Up to certain level most of the hydrolysable and free compounds disappeared.

2 Polycondensation

Remaining “humic acid” (residue left from micro-organism) incorporated into new polymeric insoluble structures (humic compounds)
Humic acid; results from the polycondensation of Organic residue of microbial metabolism (more or less oxidizing condition)
Oxidative condensation of Phenol is important process: addition of nitrogenous compound--- occur---through random polymerization-- -of free radicle like semiquinone
Soil humic acid structure (swaim, 1963): polycondensates made of nuclei bearing reactive groups; connected by bridges
a) nuclei: simple/or condensed aromatic/naphtenic
b) bridges: oxygen, sulphur, peptide or methylene bonds
Important reactive group is OH

3 Insolubilization

Decomposition + Polycondensation: first few meters of sediments; which represents 90% of total organic matter in young sediments
With increase in depth fulvic + humic acid converted into humin (insoluble)
Insolubilization occurs during diagenesis on a wider scale w.r.t time and depth (greater time and greater depth w.r.t other two steps)

Two stages: 1st Initial Stage
 First 10m: humic acid fraction
Shows loss of peptide bonds
Decrease of hydrolyzable nitrogen and N/C ratio: elimination of N from solid organic phase (expulsion of N): thus amonia increases in pore water
Result: during same interval: carboxylic and aliphatic group increases
2nd Step  10m-100m
Over this interval: oxygen content reduced
O/C ratio ranges from 0.3-0.6 in young humic acid sediments to
1-0.2 in kerogen: related to elimination of carboxylic acid group.

Source Rock:

“sedimentary rock in which organic material under pressure, heat and time is transferred into liquid/gas hydrocarbons” usually shales and limestone.

Result and Sumary of Diagenesis

OM present within water and sediments degraded by organisms and used in metabolism.
Even in fine mud, part of OM has been consumed
Other part used in constituents of organism cell and enter to biological cycle. The OM lost is about 15-50% of Original by decay
The residue left polymerized or condensed into new form insoluble kerogen. This reaction takes place under mild T and P
Besides kerogen, OM still comparises at the end of diagenesis a minor amount of free hydrocarbons and related compounds, which are synthesized by organism and incorporated into sediments with no or little change, called as geochemical fossils (witnessing the depositional environment).