CN112820363A - Effective hydrocarbon source rock organic carbon lower limit determination method - Google Patents

Effective hydrocarbon source rock organic carbon lower limit determination method Download PDF

Info

Publication number
CN112820363A
CN112820363A CN201911127594.1A CN201911127594A CN112820363A CN 112820363 A CN112820363 A CN 112820363A CN 201911127594 A CN201911127594 A CN 201911127594A CN 112820363 A CN112820363 A CN 112820363A
Authority
CN
China
Prior art keywords
hydrocarbon
organic carbon
rock
source rock
calculating
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN201911127594.1A
Other languages
Chinese (zh)
Other versions
CN112820363B (en
Inventor
杨一鸣
黄双泉
王延山
徐建斌
刘海艳
徐锐
程春阳
王群一
李宗亮
李晶晶
姚群涛
杨时杰
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Petrochina Co Ltd
Original Assignee
Petrochina Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Petrochina Co Ltd filed Critical Petrochina Co Ltd
Priority to CN201911127594.1A priority Critical patent/CN112820363B/en
Publication of CN112820363A publication Critical patent/CN112820363A/en
Application granted granted Critical
Publication of CN112820363B publication Critical patent/CN112820363B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16CCOMPUTATIONAL CHEMISTRY; CHEMOINFORMATICS; COMPUTATIONAL MATERIALS SCIENCE
    • G16C99/00Subject matter not provided for in other groups of this subclass

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Bioinformatics & Computational Biology (AREA)
  • Computing Systems (AREA)
  • Theoretical Computer Science (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Abstract

The invention discloses a method for determining the lower limit of organic carbon of an effective hydrocarbon source rock. The method comprises the following steps: calculating the hydrocarbon content in the source rock when a certain depth reaches a critical saturation degree; calculating the initial hydrocarbon generation potential: calculating the conversion rate of the corresponding organic matter into hydrocarbon according to the depth; then, according to the conversion rate, calculating the initial hydrocarbon generation potential by the content of the hydrocarbon required during hydrocarbon discharge; calculating the required organic carbon content in the source rock when discharging hydrocarbons: and (3) making a correlation graph of the hydrocarbon generation potential and the organic carbon content TOC according to rock pyrolysis data to obtain a fitting relational expression of the hydrocarbon generation potential and the organic carbon content TOC of different types of hydrocarbon source rocks, and calculating the organic carbon content required by the source rocks when the hydrocarbon is discharged at different depths according to the fitting relational expression. The method is convenient and quick, and the lower limit of the organic carbon of the effective hydrocarbon source rock with different oil drainage saturation degrees can be determined by using relatively common organic carbon and rock pyrolysis test items in a geochemical method.

Description

Effective hydrocarbon source rock organic carbon lower limit determination method
Technical Field
The invention belongs to the technical field of resource evaluation in oil-gas geology; in particular to a method for determining the lower limit of organic carbon of an effective hydrocarbon source rock.
Background
The focus in the evaluation of the effective hydrocarbon source rock is 'what organic matter abundance lower limit is adopted', which relates to what rock is the effective hydrocarbon source rock, how thick the effective hydrocarbon source layer is, and how large the distribution area and the volume of the effective hydrocarbon source layer are. As early as 20 years ago, Jones (1978) pointed out that "the minimum organic carbon content necessary to make a potential parent rock effective, rather than a constant, varied widely depending on many other variables, i.e., in theory, source rocks of different basins, different depositional environments, different organic matter types, different maturity, should have different lower organic matter abundance limits; however, in practical work, a uniform lower limit of the abundance of the organic matter is often adopted for convenient operation. In order to ensure sufficient hydrocarbon production and sufficient drainage efficiency, an effective source rock must have a corresponding abundance of organic matter (and its type, maturity and associated physical and chemical conditions). For the lower limit of organic carbon, Jones considers 2.5%. The majority of the world's important reservoirs are produced primarily from 2.5% by weight of parent rock in total organic carbon, and often in the range of over 10%. There are many examples such as Merilidian, Allan and Riya species, Calif. Shandong Mitsuda, Chalker series black shale in the Bay of Pradenhua, Baken and Wudford in the Central continental, West Siberian Zhongsheng, etc. The lower limit of organic carbon is more than or equal to 1% by the scholars of Momper, McAulif fe, Barker, etc. They indicate that potential parent rocks containing 0.5% to 1% organic carbon, although some amount of hydrocarbons may be produced, often do not form an effective "self-expulsion mechanism" - -such as an effective crack opening, "three-dimensional kerogen network" formation, "hydrocarbon pore center network" formed by the coalescence of isolated oil droplets, and the like. Only a small fraction of the potential parent rocks are actually "actually involved in the flooding process", and perhaps most kerogen families are actually non-petrochemicals. The lower limit of the abundance of the organic matters proposed by most scholars in China is obviously lower than the international standard, the lower limit of the abundance of the organic matters of the carbonate hydrocarbon source rock is considered to be 0.1-0.2%, and the lower limit of the abundance of the organic matters of the carbonate widely adopted by field exploration departments is 0.1%; the lower limit of the organic matter abundance of the marine-facies argillaceous source rock is 0.5 percent, and the lower limit is the same as that of the land-facies (lake-facies) argillaceous source rock. With regard to mudstone as a hydrocarbon source rock, the evaluation standard of mudstone is currently more uniform in the petroleum industry, and the organic carbon content of 0.4% is used as the boundary between non-oil-producing rock and oil-producing rock, while the evaluation standard of mudstone as an effective hydrocarbon source rock is still widely divergent and varies from 0.4%, 0.5%, 0.7%, 1.0% and even larger.
Disclosure of Invention
In order to solve the technical problem of difficult definition of organic carbon of the effective source rock, the invention provides a method for determining the lower limit of the organic carbon of the effective source rock, which determines the lower limit of the organic carbon of the effective source rock by utilizing the relation among the critical saturation of oil discharge, the hydrocarbon content during the oil discharge and the hydrocarbon generation potential, points out the vertical and horizontal spreading range and the distribution rule of the organic carbon of the effective source rock, and guides the oil-gas exploration and development.
In order to achieve the purpose, the invention adopts the following technical scheme:
a method for determining the lower limit of organic carbon of an effective hydrocarbon source rock comprises the following steps:
s100: calculating the hydrocarbon content in the source rock when a certain depth reaches a critical saturation degree;
s200: calculating initial hydrocarbon generation potential;
s300: the desired organic carbon content in the source rock at the time of hydrocarbon expulsion was calculated.
Preferably, the step of S200 calculating the initial hydrocarbon generation potential comprises:
calculating the conversion rate of the corresponding organic matter into hydrocarbon according to the depth; then, the initial hydrocarbon generation potential is calculated from the hydrocarbon content required during the hydrocarbon discharge according to the conversion rate.
Preferably, the step of S300 calculating the required organic carbon content in the source rock upon expulsion of hydrocarbons comprises:
and (3) making a correlation graph of the hydrocarbon generation potential and the organic carbon content TOC according to rock pyrolysis data to obtain a fitting relational expression of the hydrocarbon generation potential and the organic carbon content TOC of different types of hydrocarbon source rocks, and calculating the organic carbon content required by the source rocks when the hydrocarbon is discharged at different depths according to the fitting relational expression.
In a preferred embodiment of the present invention, there is provided a method for determining the lower limit of organic carbon in an effective source rock, comprising the steps of:
s100: calculating the hydrocarbon content in the source rock when the critical saturation is reached at a certain depth:
the invention discloses a research premise of organic carbon abundance lower limit of effective hydrocarbon source rock, which comprises the following 4 assumptions:
(1) mudstone porosity decreases with depth;
(2) the primary migration phase is a continuous oil phase and the critical saturation is 10 percent;
(3) assuming that the available carbon is all degrading the raw hydrocarbons;
(4) the unit volume of the hydrocarbon source rock absorbs hydrocarbon (particle absorption and organic matter absorption) to a certain amount;
according to the above assumptions, the hydrocarbon content in the source rock at a certain depth (porosity) of the source rock per unit volume at the initial deposition can be obtained, and the formula is:
Figure BDA0002277343090000031
the data in the formula are determined according to the actual measurement result: HCRock-total hydrocarbon content of rock, mg/g;
V0initial Source rock volume, cm3
Figure BDA0002277343090000032
-a certain depth of porosity,%;
Srow board-critical saturation of oil discharge,%;
ρhydrocarbonsDensity of hydrocarbon fluid, mg/cm3
ρRock (A. B. EDensity of source rock in mg/cm3
S1-soluble hydrocarbons in rock pyrolysis report, mg/g;
s200: calculating the initial hydrocarbon generation potential:
calculating the conversion rate of the corresponding organic matter into hydrocarbon according to the depth; then, according to the conversion rate, calculating the initial hydrocarbon generation potential by the content of the hydrocarbon required during hydrocarbon discharge;
wherein, according to the hydrocarbon generation dynamics experimental data, a conversion rate and depth change formula is simulated, as shown in figure 2; the formula of the conversion rate and the depth change of organic matters in the source rock at a certain moment in the process of the geological history is as follows:
<3000m:y=405.68ln(x)+3253.2;
≥3000m:y=21261x2-29263x+12969;
wherein x is the conversion, i.e. the total hydrocarbon yield, mg/g; y is depth, m;
s300: calculating the required organic carbon content in the source rock when discharging hydrocarbons:
the hydrocarbon generation potential of different types of hydrocarbon source rocks is different, and the hydrocarbon generation potential (S1+ S2) and the organic carbon content TOC can be plotted according to rock pyrolysis data (Tmax is less than 435 ℃); the fitting relations of the type III, type II and type I organic matters are respectively as follows:
S1+S2=109.82TOC-0.5;
S1+S2=328.09TOC-0.5;
S1+S2=747.21TOC-0.5;
wherein S1 is soluble hydrocarbon in a rock pyrolysis report, mg/g; s2 pyrolysis hydrocarbon, mg/g;
based on the relation, the organic carbon content required by various hydrocarbon source rocks during hydrocarbon discharge with different porosities (depths) can be obtained.
In fact, complete degradation of organic matter in source rock requires a higher degree of thermal evolution, i.e. over-maturation. From the actual data, Ro (maturity of source rock) reaches 2% at 5000 m. The original organic carbon value required by discharging hydrocarbon at 5000 meters is taken as the standard of the source rock. The organic carbon standards required for different vent saturations are shown in table 1:
table 1 different effluent hydrocarbon saturation requirements organic carbon standards
Figure BDA0002277343090000041
According to the actual situation, the organic carbon standard at 10% of oil drainage saturation is reasonable, namely the organic carbon standard of the type I hydrocarbon source rock is 0.18%, the organic carbon standard of the type II hydrocarbon source rock is 0.4%, and the organic carbon standard of the type III hydrocarbon source rock is 1.1%. The organic carbon standard at different depths can be obtained according to a conversion rate and depth change formula.
Compared with the prior art, the method for determining the lower limit of the organic carbon of the effective source rock has the following beneficial effects:
1) the TOC lower limit is determined reasonably by using a formula summarized from experimental data, the TOC lower limit of the effective hydrocarbon source rock organic carbon in different regions can be determined according to the distribution characteristics of the sample points in different regions, and the method is suitable for other types of regions with complicated geological conditions, variable sedimentation characteristics and dispersed sample points.
2) The method has the characteristics of convenience and quickness, and the lower limit of the organic carbon of the effective source rock with different oil drainage saturation can be determined by using relatively common organic carbon and rock pyrolysis test items in a geochemical method.
Drawings
FIG. 1 is a flow chart of a method for determining the lower limit of organic carbon in an effective source rock according to the present invention.
FIG. 2 is a graph of conversion as a function of depth.
FIG. 3 is a graph of the correlation of organic carbon content and hydrocarbon potential of type III source rock.
FIG. 4 is a graph of the correlation of organic carbon content and hydrocarbon potential of type II source rock.
FIG. 5 is a graph of the correlation of organic carbon content and hydrocarbon potential of type I source rock.
Detailed Description
In order to more clearly illustrate the invention, the invention is further described below in connection with preferred embodiments. It is to be understood by persons skilled in the art that the following detailed description is illustrative and not restrictive, and is not to be taken as limiting the scope of the invention.
The effective source rock partitioning is performed by taking the L-pit S area as an example. The ancient climate in the sand three period generally changes from early semiarid to late semihumid, and the water body gradually desalts. The early and middle stages of sand, water and water are changed into warm and wet, the water quantity is rich, the evaporation is weakened, the lake surface rises due to the rapid sinking of the basin, the lake water deepens and widens, the sediment differentiation is obvious, and the sediment has the characteristics of rapid sedimentation and rapid filling. The three-section hydrocarbon source rock is mainly dark mudstone, is wide in distribution and large in overall thickness, and has good conditions for determining the lower limit of organic carbon of the effective hydrocarbon source rock by using the method.
The method for determining the lower limit of organic carbon of the effective source rock is according to the flow shown in figure 1, and comprises the following steps:
s100: hydrocarbon content in source rock at critical saturation:
the lower limit research premise of the organic carbon abundance of the effective source rock comprises the following 4 assumptions:
1) mudstone porosity decreases with depth;
2) the primary migration phase is a continuous oil phase and the critical saturation is 10 percent;
3) assuming that the available carbon is all degrading the raw hydrocarbons;
4) the unit volume of the source rock absorbs hydrocarbons (particle absorption, organic matter absorption) to a certain amount.
According to the hypothesis, the hydrocarbon content of the source rock when the unit volume of the source rock reaches the critical saturation when the initial deposition is 5000m can be obtained, and the formula is as follows:
Figure BDA0002277343090000051
the data in the formula are determined according to the actual measurement result: HCRock-total hydrocarbon content of rock, mg/g;
V0initial Source rock volume, cm3
Figure BDA0002277343090000052
-a certain depth of porosity,%;
Srow board-critical saturation of oil discharge,%;
ρhydrocarbonsDensity of hydrocarbon fluid, mg/cm3
ρRock (A. B. EDensity of source rock in mg/cm3
S1-soluble hydrocarbons in rock pyrolysis report, mg/g.
S200: initial hydrocarbon generation potential. According to the conversion rate of organic matters in the source rock at each moment in the process of the geological history, the initial hydrocarbon generation potential can be calculated according to the required hydrocarbon content during the hydrocarbon discharge.
The conversion calculation process is conventional in the art, for example, in the embodiment of the present invention, the hydrocarbon generation kinetics experiment is performed by taking core from 200m to 5000m, and core every 200m, and the kerogen oil yield, oil cracking gas yield, kerogen gas yield, cumulative oil yield, total gas yield, the conversion x calculated finally, and the fitting formula shown in fig. 2 are as follows:
<3000m:y=405.68㏑(x)+3253.2;
≥3000m:y=21261x2-29263x+12969;
wherein x is the conversion, i.e. the total hydrocarbon yield, mg/g; y is depth, m.
The data measured during the conversion calculation in this example are shown in table 2:
TABLE 2 data sheet of experimentally determined conversion
Figure BDA0002277343090000061
S300: the desired organic carbon content in the source rock at the time of hydrocarbon expulsion was calculated. The hydrocarbon generation potential of different types of hydrocarbon source rocks is different, and the hydrocarbon generation potential and the organic carbon content of the rocks can be plotted according to rock pyrolysis data (Tmax is less than 435 ℃). As will be appreciated by those skilled in the art, the data of S1 and S2 are obtained from the rock pyrolysis data report, and different values are obtained at different depths, and then a corresponding relationship fit is found according to the total organic carbon data, as shown in FIGS. 3-5, FIG. 3 is a graph of the correlation between the organic carbon content and the hydrocarbon-forming potential of type III rock, FIG. 4 is a graph of the correlation between the organic carbon content and the hydrocarbon-forming potential of type II rock, and FIG. 5 is a graph of the correlation between the organic carbon content and the hydrocarbon-forming potential of type I rock.
The fitting relations of the type III, type II and type I organic matters are respectively as follows:
S1+S2=109.82TOC-0.5;
S1+S2=328.09TOC-0.5;
S1+S2=747.21TOC-0.5;
wherein S1 is soluble hydrocarbon in a rock pyrolysis report, mg/g; s2 pyrolysis of hydrocarbons, mg/g.
Based on the relational expression, the organic carbon standard at 10% of oil drainage saturation is reasonable, and the lower limit standard of the organic carbon of the source rock at different depths can be obtained. When the source rock buried depth reaches 5000 meters and the organic matter is completely degraded, as can be seen from table 1, the organic carbon standard of type i source rock is 0.18%, the organic carbon standard of type ii source rock is 0.4%, and the organic carbon standard of type iii source rock is 1.1%.
It should be understood that the above-mentioned embodiments of the present invention are only examples for clearly illustrating the present invention, and are not intended to limit the embodiments of the present invention, and it will be obvious to those skilled in the art that other variations or modifications may be made on the basis of the above description, and all embodiments may not be exhaustive, and all obvious variations or modifications may be included within the scope of the present invention.

Claims (10)

1. A method for determining the lower limit of organic carbon of an effective hydrocarbon source rock is characterized by comprising the following steps:
s100: calculating the hydrocarbon content in the source rock when a certain depth reaches a critical saturation degree;
s200: calculating initial hydrocarbon generation potential;
s300: the desired organic carbon content in the source rock at the time of hydrocarbon expulsion was calculated.
2. The method for determining the lower organic carbon limit of an effective hydrocarbon source rock according to claim 1, wherein the step of S200 calculating the initial hydrocarbon generation potential comprises:
calculating the conversion rate of the corresponding organic matter into hydrocarbon according to the depth; then, the initial hydrocarbon generation potential is calculated from the hydrocarbon content required during the hydrocarbon discharge according to the conversion rate.
3. The method of claim 2, wherein the step of S300 calculating the required organic carbon content in the source rock for expulsion of hydrocarbons comprises:
and (3) making a correlation graph of the hydrocarbon generation potential and the organic carbon content TOC according to rock pyrolysis data to obtain a fitting relational expression of the hydrocarbon generation potential and the organic carbon content TOC of different types of hydrocarbon source rocks, and calculating the organic carbon content required by the source rocks when the hydrocarbon is discharged at different depths according to the fitting relational expression.
4. The method for determining the lower organic carbon limit of an effective source rock according to claim 1, comprising the steps of:
s100: calculating the hydrocarbon content in the source rock when a certain depth reaches a critical saturation degree;
s200: calculating the initial hydrocarbon generation potential:
calculating the conversion rate of the corresponding organic matter into hydrocarbon according to the depth; then, according to the conversion rate, calculating the initial hydrocarbon generation potential by the content of the hydrocarbon required during hydrocarbon discharge;
s300: calculating the required organic carbon content in the source rock when discharging hydrocarbons:
and (3) making a correlation graph of the hydrocarbon generation potential and the organic carbon content TOC according to rock pyrolysis data to obtain a fitting relational expression of the hydrocarbon generation potential and the organic carbon content TOC of different types of hydrocarbon source rocks, and calculating the organic carbon content required by the source rocks when the hydrocarbon is discharged at different depths according to the fitting relational expression.
5. The method for determining the lower organic carbon limit of an effective source rock according to any one of claims 1 to 4, wherein the research premise of the method comprises the following 4-point hypothesis:
1) mudstone porosity decreases with depth;
2) the primary migration phase is a continuous oil phase and the critical saturation is 10 percent;
3) assuming that the available carbon is all degrading the raw hydrocarbons;
4) the source rock adsorbs a certain amount of hydrocarbons per unit volume.
6. The method for determining the lower limit of the effective organic carbon of the source rock according to claim 5, wherein in S100, the formula of the hydrocarbon content in the source rock when the critical saturation is reached at a certain depth per unit volume of the source rock during initial deposition is as follows:
Figure FDA0002277343080000021
the data in the formula are determined according to the actual measurement result: HCRock-total hydrocarbon content of rock, mg/g;
V0initial source rock massVolume, cm3
Figure FDA0002277343080000022
-a certain depth of porosity,%;
Srow board-critical saturation of oil discharge,%;
ρhydrocarbonsDensity of hydrocarbon fluid, mg/cm3
ρRock (A. B. EDensity of source rock in mg/cm3
S1-soluble hydrocarbons in rock pyrolysis report, mg/g.
7. The method for determining the lower limit of organic carbon in effective source rock according to claim 6, wherein in S200, the formula of the conversion rate and the depth change of organic matters in the source rock at a certain moment in the process of the geological history is as follows:
<3000m:y=405.68ln(x)+3253.2;
≥3000m:y=21261x2-29263x+12969;
wherein x is the conversion, i.e. the total hydrocarbon yield, mg/g; y is depth, m.
8. The method for determining the lower limit of organic carbon in effective source rock according to claim 7, wherein in S300, the fitting relations between the hydrocarbon generation potential and the organic carbon content TOC of the type III, type II and type I source rock are respectively as follows:
S1+S2=109.82TOC-0.5;
S1+S2=328.09TOC-0.5;
S1+S2=747.21TOC-0.5;
wherein S1 is soluble hydrocarbon in a rock pyrolysis report, mg/g; s2 pyrolysis of hydrocarbons, mg/g.
9. The method for determining the lower organic carbon limit of an effective source rock according to claim 5, comprising the steps of:
s100: calculating the hydrocarbon content in the source rock when a certain depth reaches a critical saturation degree;
the formula of the hydrocarbon content in the source rock when the unit volume of the source rock reaches the critical saturation at a certain depth during initial deposition is as follows:
Figure FDA0002277343080000023
the data in the formula are determined according to the actual measurement result: HCRock-total hydrocarbon content of rock, mg/g;
V0initial Source rock volume, cm3
Figure FDA0002277343080000031
-a certain depth of porosity,%;
Srow board-critical saturation of oil discharge,%;
ρhydrocarbonsDensity of hydrocarbon fluid, mg/cm3
ρRock (A. B. EDensity of source rock in mg/cm3
S1-soluble hydrocarbons in rock pyrolysis report, mg/g;
s200: calculating the initial hydrocarbon generation potential:
calculating the conversion rate of the corresponding organic matter into hydrocarbon according to the depth; then, according to the conversion rate, calculating the initial hydrocarbon generation potential by the content of the hydrocarbon required during hydrocarbon discharge;
the formula of the conversion rate and the depth change of organic matters in the source rock at a certain moment in the process of the geological history is as follows:
<3000m:y=405.68ln(x)+3253.2;
≥3000m:y=21261x2-29263x+12969;
wherein x is the conversion, i.e. the total hydrocarbon yield, mg/g; y is depth, m;
s300: calculating the required organic carbon content in the source rock when discharging hydrocarbons:
the hydrocarbon generation potentials of different types of hydrocarbon source rocks are different, a correlation graph of the hydrocarbon generation potential and the organic carbon content TOC is made according to rock pyrolysis data, a fitting relational expression of the hydrocarbon generation potential and the organic carbon content TOC of the different types of hydrocarbon source rocks is obtained, and the organic carbon content required in the source rocks when the various types of hydrocarbon source rocks discharge hydrocarbons at different depths is calculated according to the fitting relational expression;
fitting relations of hydrocarbon generation potential and organic carbon content TOC of type III, type II and type I hydrocarbon source rocks are respectively as follows:
S1+S2=109.82TOC-0.5;
S1+S2=328.09TOC-0.5;
S1+S2=747.21TOC-0.5;
wherein S1 is soluble hydrocarbon in a rock pyrolysis report, mg/g; s2 pyrolysis of hydrocarbons, mg/g.
10. A method for determining the lower limit of organic carbon in an effective source rock as claimed in claim 8 or 9, wherein at a depth of 5000m, the 10% drainage saturation requires the following organic carbon:
type I: 0.18 percent;
type II: 0.4 percent;
type III: 1.1 percent.
CN201911127594.1A 2019-11-18 2019-11-18 Method for determining organic carbon lower limit of effective hydrocarbon source rock Active CN112820363B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201911127594.1A CN112820363B (en) 2019-11-18 2019-11-18 Method for determining organic carbon lower limit of effective hydrocarbon source rock

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201911127594.1A CN112820363B (en) 2019-11-18 2019-11-18 Method for determining organic carbon lower limit of effective hydrocarbon source rock

Publications (2)

Publication Number Publication Date
CN112820363A true CN112820363A (en) 2021-05-18
CN112820363B CN112820363B (en) 2023-12-26

Family

ID=75852357

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201911127594.1A Active CN112820363B (en) 2019-11-18 2019-11-18 Method for determining organic carbon lower limit of effective hydrocarbon source rock

Country Status (1)

Country Link
CN (1) CN112820363B (en)

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20140136172A1 (en) * 2012-04-18 2014-05-15 Landmark Graphics Corporation Methods and systems of modeling hydrocarbon flow from layered shale formations
CN104533406A (en) * 2015-01-15 2015-04-22 中国石油大学(北京) Method for determining petroleum entrapment probability
CN105486768A (en) * 2015-12-08 2016-04-13 中国石油大学(北京) Defining method of hydrocarbon expulsion source rock
CN106326516A (en) * 2015-07-02 2017-01-11 中国石油天然气股份有限公司 Establishment method for hydrocarbon expulsion function and hydrocarbon expulsion index function of hydrocarbon source rocks
CN109709299A (en) * 2018-11-16 2019-05-03 中国石油天然气股份有限公司 A kind of organic carbon recovering coefficient evaluation method based on hydrocarbon source rock life residence rate

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20140136172A1 (en) * 2012-04-18 2014-05-15 Landmark Graphics Corporation Methods and systems of modeling hydrocarbon flow from layered shale formations
CN104533406A (en) * 2015-01-15 2015-04-22 中国石油大学(北京) Method for determining petroleum entrapment probability
CN106326516A (en) * 2015-07-02 2017-01-11 中国石油天然气股份有限公司 Establishment method for hydrocarbon expulsion function and hydrocarbon expulsion index function of hydrocarbon source rocks
CN105486768A (en) * 2015-12-08 2016-04-13 中国石油大学(北京) Defining method of hydrocarbon expulsion source rock
CN109709299A (en) * 2018-11-16 2019-05-03 中国石油天然气股份有限公司 A kind of organic carbon recovering coefficient evaluation method based on hydrocarbon source rock life residence rate

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
周总瑛;: "烃源岩演化中有机碳质量与含量变化定量分析", 石油勘探与开发, no. 04 *

Also Published As

Publication number Publication date
CN112820363B (en) 2023-12-26

Similar Documents

Publication Publication Date Title
Xuanjun et al. Lacustrine fine-grained sedimentary features and organicrich shale distribution pattern: A case study of Chang 7 Member of Triassic Yanchang Formation in Ordos Basin, NW China
CN111694068B (en) Large-scale fresh water lake basin continental facies mud shale oil formation and enrichment evaluation method
Caineng et al. Formation and distribution of “continuous” gas reservoirs nd their giant gas province: a case from the Upper riassic Xujiahe Formation giant gas province, Sichuan Basin
CN110412661B (en) Evaluation method and device for dominant segment cluster of fine-grained rock oil and gas reservoir dessert segment
Stonecipher et al. Diagenesis of the Frontier Formation, Moxa Arch: A Function of Sandstone Geometry, Texture and Composition, and Fluid Flux: Part 3. Applications in Exploration and Production
Xinshan et al. Gas exploration potential of tight carbonate reservoirs: A case study of Ordovician Majiagou Formation in the eastern Yi-Shan slope, Ordos Basin, NW China
Suyun et al. Heterogeneous geological conditions and differential enrichment of medium and high maturity continental shale oil in China
CN104007482A (en) Shale rock physical model method based on anisotropic effective field
CN112147301B (en) Quantitative evaluation method for effectiveness of dense oil hydrocarbon source rock of land freshwater lake basin
CN108088779B (en) Reservoir space classification method for compact reservoir and conventional reservoir
Liu et al. Dynamic conditions of Mesozoic petroleum secondary migration, Ordos Basin
Guangyou et al. Distribution characteristics of effective source rocks and their control on hydrocarbon accumulation: a case study from the Dongying Sag, Eastern China
Zou et al. Prospect of ultra-deep petroleum onshore China
Trewin et al. The Auk Field, Block 30/16, UK North Sea
Simmons et al. Modelling density-dependent flow and solute transport at the Lake Tutchewop saline disposal complex, Victoria
Liu et al. The Control Theory and Application for Well Pattern Optimization of Heterogeneous Sandstone Reservoirs
CN112820363A (en) Effective hydrocarbon source rock organic carbon lower limit determination method
Jia et al. Petroleum geological characteristics of Kela-2 gas field
Gerhart A model of regional ground‐water flow in secondary‐permeability terrane
CN107478768A (en) A kind of mud shale Gu shearing strength determines method
Li et al. Deepening research on the distribution characteristics of interlayers in marine sandstone reservoirs
CN111027780A (en) Oil potential field simulation method and device
Wang et al. High‐Frequency Sequence Stratigraphy and Fine‐Scale Reservoir Characterization of the Devonian Sandstone, Donghe Formation, North Uplift of the Tarim Basin
Chowdhury et al. Porosity evolution in the Albert Formation of the Stoney Creek oil and gas field, Moncton subbasin, New Brunswick, Canada
Yin et al. Oil Accumulation Model and Its Main Controlling Factors in Lower Yanchang Formation, Wuqi‐Dingbianarea, Ordos Basin, China

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant