CN104700316B - A method for evaluating oil and gas generation of shale by heterogeneity - Google Patents
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Abstract
本发明涉及一种非均质性评价泥页岩生油气量的方法,含有以下步骤:一、对泥页岩剖面上不同深度点密集采样,并通过Rock-Eval热解检测获取基本参数值,确定有机质类型;二、建立概念模型并计算不同形式的有机碳含量;三、设计模拟实验,建立重烃油产率和天然气产率演化模型。四、计算泥页岩不同深度点生成和排出的总烃量以及重质油量、轻质油量和生气量,评价泥页岩含油性和含气性的非均质性。本发明模型是建立在剖面大量样品数据点之上,可对泥页岩油气资源进行非均质性评价,当在样品有限情况下,结合测井资料本发明仍然适用,因此对定量表征泥页岩含油气性的非均质性和准确评价非常规泥页岩油气资源有重要的意义。
The invention relates to a method for evaluating the oil and gas generation capacity of mud shale by heterogeneity, which comprises the following steps: 1. Intensively sampling points at different depths on the mud shale profile, and obtaining basic parameter values through Rock-Eval pyrolysis detection, Determine the type of organic matter; 2. Establish a conceptual model and calculate the content of organic carbon in different forms; 3. Design simulation experiments to establish the evolution model of heavy hydrocarbon oil yield and natural gas yield. 4. Calculate the total hydrocarbons generated and discharged at different depth points of shale, as well as the amount of heavy oil, light oil and gas, and evaluate the heterogeneity of oil and gas content of shale. The model of the present invention is based on a large number of sample data points in the profile, and can evaluate the heterogeneity of mud shale oil and gas resources. When the samples are limited, the present invention is still applicable in combination with logging data, so it is useful for quantitatively characterizing mud shale It is of great significance to understand the heterogeneity of oil and gas bearing properties of rocks and to accurately evaluate unconventional shale oil and gas resources.
Description
技术领域technical field
本发明属于油气勘探开发技术领域,具体地说,涉及以一种泥页岩生油气量的评价方法。The invention belongs to the technical field of oil and gas exploration and development, and in particular relates to a method for evaluating the amount of oil and gas generated by mud shale.
背景技术Background technique
由于不断攀升的能源需求和日益增大的能源压力,让泥页岩油气这一非常规能源受到越来越多的重视。美国对泥页岩的勘探开发走在世界的前列,是目前泥页岩气大规模商业开发取得成功的唯一国家。1976年,美国能源部开始关注东部页岩气,就Antrim页岩、Ohio页岩、NewAlbany页岩、Barnett页岩和Lewis页岩等五大页岩气系统开展了针对页岩气地质、地球化学和石油工程的研究(Curtis,2002)。加拿大紧随其后,近年来也开展了页岩气的勘探及实验研究,对泥盆系、石炭系和侏罗系页岩气的勘探潜力进行了评估(RossD&Bustin,2007,2008)。Due to rising energy demand and increasing energy pressure, shale oil and gas, an unconventional energy source, has received more and more attention. The United States is at the forefront of the world in the exploration and development of mud shale, and is currently the only country that has successfully achieved large-scale commercial development of mud shale gas. In 1976, the U.S. Department of Energy began to pay attention to shale gas in the east, and carried out research on shale gas geology, geochemistry and Research in Petroleum Engineering (Curtis, 2002). Canada followed suit, and in recent years has also carried out shale gas exploration and experimental research, evaluating the exploration potential of Devonian, Carboniferous and Jurassic shale gas (Ross D & Bustin, 2007, 2008).
国内天然气资源构成中,煤系烃源岩和海相碳酸盐岩的贡献较大,并且国内的研究者及勘探家们对页岩气多关注于中国西部和南方古生代海相和煤系页岩气的形成及勘探潜力(张金川等,2003,2004,2007,2008,2009;张水昌等,2006;梁狄刚等,2008;叶军等,2008;聂海宽等,2009,2010,2011;朱华等,2009;王兰生等,2009;王世谦等,2009;徐士林等,2009;程克明等,2009;黄籍中等,2009;蒲泊伶等,2008,2010;董大忠等,2009,2010;付小东等,2011;陈尚斌等,2011;梁兴等,2011;王社教等,2011);湖相烃源岩生成的天然气所占比例较小,而来源于中国东部湖相烃源岩的页岩油气勘探在中国更是处于起步阶段。湖相烃源岩作为中国油气资源的主要生烃物质基础,与它对天然气资源的贡献比例很不对称。其主要原因是,中国多数湖盆埋藏相对较浅,没有进入高成熟成气门限。然而,中国东部湖相盆地非常富油,以东营凹陷古近系为例,是典型的富油湖盆,其中发育了大套的泥页岩,形成相对封闭的系统,大量烃类滞留其中,因此可形成丰富的非常规泥页岩油气资源。In the composition of natural gas resources in China, coal-measure source rocks and marine carbonate rocks make a greater contribution, and domestic researchers and explorers pay more attention to shale gas in the Paleozoic marine and coal-measure shale in western and southern China. Formation and exploration potential of rock gas (Zhang Jinchuan et al., 2003, 2004, 2007, 2008, 2009; Zhang Shuichang et al., 2006; Liang Digang et al., 2008; Ye Jun et al., 2008; Nie Haikuan et al., 2009, 2010, 2011; Zhu Hua et al. , 2009; Wang Lansheng et al., 2009; Wang Shiqian et al., 2009; Xu Shilin et al., 2009; Cheng Keming et al., 2009; Huang Jizhong et al., 2009; Pu Boling et al., 2008, 2010; ; Chen Shangbin et al., 2011; Liang Xing et al., 2011; Wang Shejiao et al., 2011); the proportion of natural gas generated from lacustrine source rocks is relatively small, and shale oil and gas exploration from lacustrine source rocks in eastern China is more popular in China. is in its infancy. Lacustrine source rocks are the main hydrocarbon-generating material basis of China's oil and gas resources, and their contribution to natural gas resources is very asymmetrical. The main reason is that most lake basins in China have relatively shallow burials and have not entered the threshold of high-maturity gas formation. However, lacustrine basins in eastern China are very oil-rich. Taking the Paleogene in the Dongying sag as an example, it is a typical oil-rich lacustrine basin, in which a large set of mud shale developed, forming a relatively closed system in which a large amount of hydrocarbons remained. Therefore, abundant unconventional shale oil and gas resources can be formed.
泥页岩中的油气资源量是固体有机质经过热演化转化成液态或气态烃后储存在泥页岩的孔隙中,表征泥页岩油气资源量的参数有原始生烃潜量(指有机质完全转化成烃的量)、生烃量(目前已经生成烃的量)、排烃量(生成烃并排出自身岩石的量)和排烃系数等(排烃量占生烃量的比例),这些参数的确定都与泥页岩中的有机碳含量有关。由于断陷陆相湖盆烃源岩存在严重的非均质性,表现为有机质分布的非均质性和源岩压实的不均衡性,因此,这导致烃源岩中烃类的生成和排出通常不是均匀和连续的,从而引起泥页岩系统中油气资源分布的非均质性。The amount of oil and gas resources in shale is that solid organic matter is transformed into liquid or gaseous hydrocarbons through thermal evolution and stored in the pores of shale. amount of hydrocarbon generation), hydrocarbon generation amount (the amount of hydrocarbons that have been generated so far), hydrocarbon expulsion amount (the amount of hydrocarbons generated and expelled from its own rocks), and hydrocarbon expulsion coefficient (the ratio of hydrocarbon expulsion amount to hydrocarbon generation amount), these parameters All determinations are related to the organic carbon content in the shale. Due to the serious heterogeneity of source rocks in faulted continental lacustrine basins, manifested as the heterogeneity of organic matter distribution and the unbalanced compaction of source rocks, the generation and discharge of hydrocarbons in source rocks are usually It is not uniform and continuous, which leads to the heterogeneity of the distribution of oil and gas resources in the shale system.
世界上成功勘探开发页岩油气的北美地区关于页岩油气具有富集、可采性的基本标准是:有机质丰度较高、成熟度较高、一般有机质类型较好、脆性矿物含量较高(粘土矿物含量较低)。然而,在我国陆相盆地,尤其是东部的断陷盆地,沉积相变化频繁,泥页岩中有机质分布非均质性强。因此,对中国湖相特色的泥页岩油气资源需要有一套操作性强的、行之有效的评价方法。The basic standards for enrichment and recoverability of shale oil and gas in North America, where shale oil and gas have been successfully explored and developed in the world, are: higher abundance of organic matter, higher maturity, better type of organic matter, and higher content of brittle minerals ( low content of clay minerals). However, in my country's continental basins, especially the faulted basins in the east, sedimentary facies changes frequently, and the distribution of organic matter in shale is highly heterogeneous. Therefore, it is necessary to have a set of highly operable and effective evaluation methods for the mud shale oil and gas resources with lacustrine characteristics in China.
目前由中国石油天然气股份有限责任公司和研究机构提出并被应用的生烃量定量评价方法概括起来尅分分为三类:1、改进的氯仿沥青法;2、基于有机质成烃机理的成烃率法(热模拟实验法、化学动力学法、物质平衡法);3、生烃势指数法。但现有对泥页岩油气资源的评价方法还存在以下缺点或问题:At present, the quantitative evaluation methods of hydrocarbon generation proposed and applied by China National Petroleum Corporation and research institutes can be summarized into three categories: 1. Improved chloroform asphalt method; 2. Hydrocarbon generation based on the mechanism of organic matter hydrocarbon generation Rate method (thermal simulation experiment method, chemical kinetic method, material balance method); 3. Hydrocarbon generation potential index method. However, the existing evaluation methods for shale oil and gas resources still have the following shortcomings or problems:
(1)现有的方法多算出的基于目前实测有机碳含量的生烃量,而目前实测有机碳含量实际为生烃后残留的有机碳含量,通过测井信息预测的有机碳含量实际也为残留有机碳含量;基于油气的生成量是由已转化的有机碳决定的,已转化的有机碳转化成烃而排出,形成油气资源量,因此不同的有机碳形式(如原始有机碳含量、排出有机碳含量等)对准确评价泥页岩油气资源也很重要,目前已有的方法不能满足新的需要。(1) The existing method mostly calculates the amount of hydrocarbon generation based on the current measured organic carbon content, but the current measured organic carbon content is actually the residual organic carbon content after hydrocarbon generation, and the organic carbon content predicted by well logging information is actually Residual organic carbon content; based on the fact that the generation of oil and gas is determined by the converted organic carbon, the converted organic carbon is converted into hydrocarbons and discharged to form oil and gas resources, so different forms of organic carbon (such as original organic carbon content, discharged Organic carbon content, etc.) is also very important to accurately evaluate shale oil and gas resources, and the existing methods cannot meet the new needs.
(2)现有的泥页岩生烃量的评价参数十分有限,通常是基于氯仿沥青“A”、残留生烃潜力S1+S2、残留有机碳含量TOC,因为这些参数都是可直接检测的,并不需要推算。经推算的少量参数多为生烃量Q,这个参数往往也是用体积法估测的。因此,有限的参数不能满足对泥页岩油气资源的准确评价。(2) The existing evaluation parameters of shale hydrocarbon generation are very limited, usually based on chloroform bitumen “A”, residual hydrocarbon generation potential S1+S2, and residual organic carbon content TOC, because these parameters can be directly detected , no calculation is required. Most of the estimated few parameters are the amount of hydrocarbon generation Q, which is often estimated by the volumetric method. Therefore, limited parameters cannot satisfy the accurate evaluation of shale oil and gas resources.
(3)现有的泥页岩油气资源评价通常是评价页岩气,这是由于评价地区如北美和中国西部高成熟碳酸盐盆地成熟度都很高,几乎都为气,油量很少;近几年中国东部互相盆地的页岩油也逐渐受到重视。然而,这些评价思路也不能满足需要。譬如,中国东部渤海湾盆地东营凹陷古近系深层具有相对较好的湖相页岩气形成条件,该凹陷就发育沙四上亚段和沙三下亚段烃源岩,埋藏相对较深,生成油的同时亦有部分天然气生成,因此如何同时评价泥页岩油和气是一个很重要的问题。并且,已有的油、气评价中,没有将重质油和轻质油(C6-C13轻烃)分开,这是由于轻质油在检测中容易漏失。(3) The existing evaluation of shale oil and gas resources usually evaluates shale gas. This is because the evaluation areas such as North America and western China have high maturity, almost all of them are gas, and the amount of oil is very small. ; In recent years, shale oil in mutual basins in eastern China has also gradually received attention. However, these evaluation ideas can not meet the needs. For example, the deep layers of Paleogene in the Dongying Sag, Bohai Bay Basin, East China have relatively good conditions for the formation of lacustrine shale gas. In this sag, the source rocks of the upper submember of the fourth member of the Shahejie Formation and the lower submember of the third member of the Shahejie Formation are developed. Some natural gas is also generated along with oil, so how to evaluate shale oil and gas at the same time is a very important issue. Moreover, in the existing oil and gas evaluation, heavy oil and light oil (C6-C13 light hydrocarbons) are not separated, because light oil is easy to leak during detection.
(4)现有对泥页岩生烃评价的研究工作多是局限于对烃源岩有限的取样点进行地球化学测试、分析。其重要原因在于,目前成功勘探开发页岩油气的北美地区基本是在相对比较均匀的海相地层中,其相变小,均质性较强,利用有限的实验室分析资料基本可以确定页岩油气的有利发育区和空间发育。然而,由于陆相泥页岩存在严重的非均质性和生、排烃问题的复杂性,有限的取样测试点不能客观地反映复杂的地质情况,更难以有效地对垂向上连续分布的泥页岩进行高分辨率评价,也难以确定厚层烃源岩中存在的有机质含量高、生排烃效率高的薄层优质泥页岩,这影响到勘探部署,如哪些资源是近期可以有效开采的,哪些资源是可以作为远景资源等待技术进步才能有效开采,哪些资源是没有经济价值的,因此阻碍了油气评价及勘探的进步。并且,基于样品的实测资料进行评价,存在测量方法昂贵、成本高的特点。(4) Most of the existing research work on hydrocarbon generation evaluation of shale is limited to geochemical testing and analysis of limited sampling points of source rocks. The important reason is that the successful exploration and development of shale oil and gas in North America is basically in relatively uniform marine strata, with small facies change and strong homogeneity, and shale oil and gas can basically be determined using limited laboratory analysis data. Favorable development areas and spatial development of oil and gas. However, due to the serious heterogeneity of continental mud shale and the complexity of hydrocarbon generation and expulsion problems, limited sampling test points cannot objectively reflect the complex geological conditions, and it is even more difficult to effectively analyze the vertically continuous distribution of mud shale. High-resolution evaluation of shale also makes it difficult to identify thin-layer high-quality mud shale with high organic matter content and high hydrocarbon generation and expulsion efficiency in thick source rocks, which affects exploration deployment, such as which resources can be effectively exploited in the near future What resources can be effectively exploited as prospective resources wait for technological progress, and which resources have no economic value, thus hindering the progress of oil and gas evaluation and exploration. In addition, the evaluation based on the actual measurement data of the sample has the characteristics of expensive measurement method and high cost.
综上可知,非常规泥页岩油气资源评价虽已经取得重要的进展,但是不同类型有机碳和多参数综合评价泥页岩中不同组分油气(重质油、轻质油和天然气)仍然需要期待解决。尤其是,高分辨率地对泥页岩油气生成量进行非均质性评价并指导泥页岩油气的勘探是未来泥页岩油气资源研究的一个重要的发展方向。In summary, although important progress has been made in the evaluation of unconventional shale oil and gas resources, it is still necessary to comprehensively evaluate different types of organic carbon and multi-parameter oil and gas components (heavy oil, light oil and natural gas) in shale. Looking forward to solving. In particular, evaluating the heterogeneity of shale oil and gas generation with high resolution and guiding the exploration of shale oil and gas is an important development direction for future research on shale oil and gas resources.
发明内容Contents of the invention
本发明针对现有泥页岩油气资源评价中存在的上述不足,提供了一种非均质性评价泥页岩生油气量的方法,该方法对泥页岩油气资源进行非均质性评价,对定量表征泥页岩含油气性的非均质性和准确评价非常规泥页岩油气资源有重要的意义。Aiming at the above-mentioned deficiencies existing in the evaluation of the existing mud shale oil and gas resources, the present invention provides a method for heterogeneity evaluation of mud shale oil and gas generation. The method evaluates the heterogeneity of mud shale oil and gas resources, It is of great significance to quantitatively characterize the heterogeneity of shale oil and gas and accurately evaluate unconventional shale oil and gas resources.
本发明的技术方案是:一种非均质性评价泥页岩生油气量的方法,含有以下步骤:The technical solution of the present invention is: a method for evaluating the oil and gas generation capacity of mud shale by heterogeneity, comprising the following steps:
一、对泥页岩剖面上不同深度点密集采样,并通过Rock-Eval热解检测获取基本参数值,确定有机质类型:在泥页岩剖面上深度方向每隔1-10m一个样品点进行采样,对采集的样品进行Rock-Eval热解分析,并通过Rock-Eval热解获得基本参数的参数值;根据基础参数确定每个深度样品点的氢指数HI、产率指数PI和烃指数[100×S1]/TOC,S1为岩石Rock-Eval低温阶段热解获得的游离烃,TOC为实际检测到的有机碳,通过氢指数HI和基础参数确定有机质类型。1. Intensively sample different depth points on the shale profile, and obtain basic parameter values through Rock-Eval pyrolysis detection to determine the type of organic matter: Sampling is carried out at a sample point every 1-10m in the depth direction of the shale profile. The collected samples were analyzed by Rock-Eval pyrolysis, and the parameter values of the basic parameters were obtained through Rock-Eval pyrolysis; the hydrogen index HI, the yield index PI and the hydrocarbon index [100× S 1 ]/TOC, S 1 is the free hydrocarbons obtained by pyrolysis of rocks at low temperature in the Rock-Eval stage, TOC is the actually detected organic carbon, and the type of organic matter is determined by the hydrogen index HI and basic parameters.
二、建立概念模型并计算不同形式的有机碳含量:根据有机碳的组成和转化原理,将泥页岩中有机碳分成不同有机碳形式的概念模型,将有机碳定义为残留有机碳、残留有效碳、残留无效碳、排出有机碳、排出有效碳、原始有机碳、原始有效碳、原始无效碳,泥页岩中总的原始有机碳TOC0包括排出有机碳TOCExp和残留有机碳TOCRem两部分,则存在关系式如公式(1)所示,在原始有机碳TOC0中,热解转化成烃类的有机碳部分定义为有效碳TOCrea,原始有机碳TOC0中所含有的有效碳和残留有机碳TOCRem中的有效碳分别定义为TOC0-rea和TOCRem-rea;泥页岩中残留的生烃潜力是由残留有机碳中的有效碳转化而来,它与残留有机碳TOCRem的残留降解率DRem存在的关系式如公式(2)所示;所述公式(1)和公式(2)的表达式如下:2. Establish a conceptual model and calculate the content of organic carbon in different forms: According to the composition and transformation principles of organic carbon, the organic carbon in mud shale is divided into a conceptual model of different forms of organic carbon, and organic carbon is defined as residual organic carbon, residual effective Carbon, residual ineffective carbon, excreted organic carbon, expelled effective carbon, original organic carbon, original effective carbon, original ineffective carbon, total original organic carbon TOC in mud shale includes both expelled organic carbon TOC Exp and residual organic carbon TOC Rem part, then there is a relationship as shown in formula (1), in the original organic carbon TOC 0 , the organic carbon part converted into hydrocarbons by pyrolysis is defined as the effective carbon TOC rea , and the effective carbon contained in the original organic carbon TOC 0 and the effective carbon in residual organic carbon TOC Rem are defined as TOC 0-rea and TOC Rem-rea respectively; the residual hydrocarbon generation potential in mud shale is converted from effective carbon in residual organic carbon, which is related to residual organic carbon The relational expression that the residual degradation rate D Rem of TOC Rem exists is as shown in formula (2); The expressions of described formula (1) and formula (2) are as follows:
TOC0=TOCRem+TOCExp(1)TOC 0 = TOC Rem +TOC Exp (1)
DRem=TOCRem-rea/TOCRem(2)D Rem = TOC Rem-rea /TOC Rem (2)
目前石油工业中将0.083视为碳转化为烃类的转化系数,则存在关系式如公式(3)所示,公式(3)的表达式如下:At present, 0.083 is regarded as the conversion coefficient of carbon into hydrocarbons in the petroleum industry, then there is a relational expression as shown in formula (3), and the expression of formula (3) is as follows:
TOCRem-rea=(S1+S2)×0.083(3)式中,S2为岩石Rock-Eval高温阶段热解获得的热解烃,TOC Rem-rea = (S 1 +S 2 )×0.083(3) In the formula, S 2 is the pyrolyzed hydrocarbon obtained from rock Rock-Eval high temperature stage pyrolysis,
则残留降解率DRem由公式(4)计算获得,公式(4)的表达式如下:Then the residual degradation rate D Rem is calculated by the formula (4), and the expression of the formula (4) is as follows:
DRem=(S1+S2)×0.083/TOCRem(4)D Rem = (S 1 +S 2 )×0.083/TOC Rem (4)
根据残留降解率DRem和热解峰温Tmax的交汇图确定不同有机质的原始降解潜率;The original degradation potential of different organic matter was determined according to the intersection plot of residual degradation rate D Rem and pyrolysis peak temperature T max ;
在有机质演化和成烃过程中,其中的无效碳可视为保持不变的,因此,存在关系式如公式(5)所示,公式(5)的表达式如下:In the process of organic matter evolution and hydrocarbon formation, the invalid carbon in it can be considered as constant, therefore, there is a relationship as shown in formula (5), and the expression of formula (5) is as follows:
TOC0(1–D0)=TOCRem(1–DRem)(5)TOC 0 (1–D 0 )=TOC Rem (1–D Rem )(5)
所述公式(5)中,TOC0(1–D0)代表原始有机质中的无效碳,定义为TOCIne,TOCRem(1–DRem)代表残留有机质中的无效碳,定义为TOCRem-Ine;In the formula (5), TOC 0 (1–D 0 ) represents the invalid carbon in the original organic matter, defined as TOC Ine , and TOC Rem (1–D Rem ) represents the invalid carbon in the residual organic matter, defined as TOC Rem- Ine ;
由公式(5)可转化为公式(6)和公式(7),公式(6)和公式(7)的表达式如下:Formula (5) can be transformed into formula (6) and formula (7), and the expressions of formula (6) and formula (7) are as follows:
(1–DRem)/(1–D0)=TOC0/TOCRem(6)(1–D Rem )/(1–D 0 )=TOC 0 /TOC Rem (6)
RC=TOC0/TOCRem(7)R C =TOC 0 /TOC Rem (7)
所述公式(7)中,RC为现今测得的残留有机碳到原始有机碳的恢复系数,为常量系数,无单位;In the formula (7), R C is the recovery coefficient from the residual organic carbon to the original organic carbon measured today, which is a constant coefficient and has no unit;
同时,也存在关系式如公式(8)所示,公式(8)的表达式如下:At the same time, there is also a relational expression as shown in formula (8), and the expression of formula (8) is as follows:
TOC0–TOC0-rea=TOCRem–TOCRem-rea(8)TOC 0 -TOC 0-rea = TOC Rem -TOC Rem-rea (8)
所述公式(8)中,TOC0–TOC0-rea代表原始有机质中的无效碳,定义为TOC0-Ine,TOCRem–TOCRem-rea代表残留有机质中的无效碳,定义为TOCRem-Ine;In the formula (8), TOC 0 -TOC 0-rea represents the invalid carbon in the original organic matter, which is defined as TOC 0-Ine , and TOC Rem -TOC Rem-rea represents the invalid carbon in the residual organic matter, which is defined as TOC Rem- Ine ;
通过以上公式计算出每个样品点的残留降解率DRem、原始有机碳恢复系数RC以及每种形式的有机碳含量在剖面的非均质性分布,为泥页岩油气资源评价提供基础数据;Calculate the residual degradation rate D Rem of each sample point, the original organic carbon recovery coefficient R C and the heterogeneity distribution of each form of organic carbon content in the profile through the above formula, and provide basic data for the evaluation of shale oil and gas resources ;
三、设计模拟实验,建立重烃油产率和天然气产率演化模型:选取泥页岩样品做热演化模拟实验,获取烃产率曲线,建立重质油产率和天然气产率演化模型,建立实测成熟度参数镜质体反射率VRo随深度变化模型。3. Design simulation experiments and establish heavy hydrocarbon oil yield and natural gas yield evolution models: select mud shale samples for thermal evolution simulation experiments to obtain hydrocarbon yield curves, establish heavy oil yield and natural gas yield evolution models, and establish The measured maturity parameter vitrinite reflectance VR o varies with depth.
四、计算泥页岩不同深度点生成和排出的总烃量以及重质油量、轻质油量和生气量,评价泥页岩含油性和含气性的非均质性:根据步骤一和步骤二中获得的各个参数,计算每个泥页岩样品点单位总生烃量SGen、排烃量SExp;根据步骤三中建立的模型计算每个深度点样品的油、气生成量,在获取重质油、天然气产率基础上,进一步获取C6~C14轻质油产率;进而获得每个单位样品点的重质油产率Sho、轻质油产率Slo、天然气产率Sg的分布,以定量评价泥页岩中重质油、轻质油和含气性的非均质性;通过获得的上述参数建立泥页岩生烃的评价参数剖面图,通过评价参数剖面图评价泥页岩油气资源剖面分布非均质性。4. Calculate the total hydrocarbons generated and discharged at different depth points of shale, as well as the amount of heavy oil, light oil and gas, and evaluate the heterogeneity of oil and gas content of shale: according to step 1 and For each parameter obtained in step 2, calculate the total hydrocarbon generation S Gen and hydrocarbon expulsion S Exp of each shale sample point; calculate the oil and gas generation of each depth point sample according to the model established in step 3, On the basis of obtaining heavy oil and natural gas yields, further obtain C 6 ~C 14 light oil yields; and then obtain heavy oil yields S ho , light oil yields S lo , natural gas The distribution of the yield S g is used to quantitatively evaluate the heterogeneity of heavy oil, light oil and gas-bearing properties in shale; through the above parameters obtained, the evaluation parameter profile of shale hydrocarbon generation is established, and the Evaluation of profile distribution heterogeneity of shale oil and gas resources by parameter profiles.
作为优选,步骤一中,所述的基本参数包括实测的残留有机碳TOCRem、岩石Rock-Eval低温阶段热解获得的游离烃S1、岩石Rock-Eval高温阶段热解获得的热解烃S2和热解峰温Tmax,其中,热解峰温Tmax为岩石Rock-Eval高温阶段热解获得的热解烃S2对应的峰值,实测的残留有机碳TOCRem为现今通过样品实际检测到的有机碳TOC;所述氢指数HI表示泥页岩的生烃潜力,产率指数PI表示泥页岩的成熟度和热演化,通过氢指数HI与热解峰温Tmax交汇图确定有机质类型。Preferably, in step 1, the basic parameters include measured residual organic carbon TOC Rem , free hydrocarbons S 1 obtained by pyrolysis of rock Rock-Eval low temperature stage, and pyrolyzed hydrocarbon S obtained by rock Rock-Eval high temperature stage pyrolysis 2 and the pyrolysis peak temperature T max , where the pyrolysis peak temperature T max is the peak value corresponding to the pyrolysis hydrocarbon S 2 obtained from the pyrolysis of the rock Rock-Eval high temperature stage, and the measured residual organic carbon TOC Rem is the current actual detection of the sample The organic carbon TOC obtained; the hydrogen index HI indicates the hydrocarbon generation potential of the mud shale, and the productivity index PI indicates the maturity and thermal evolution of the mud shale, and the organic matter is determined by the intersection graph of the hydrogen index HI and the pyrolysis peak temperature T max Types of.
作为优选,所述步骤三中,选取具有代表性的大块均质泥岩样品,分成9份分别放进加热釜中,做热演化模拟实验;9份样品按50℃/h的速率,分别从实验温度由室温升温至250℃、300℃、350℃、400℃、450℃、500℃、550℃、600℃,650℃9个终点温度,在每份样品到达自己的终点温度时,用恒速恒流泵以2ml/min的速率注入蒸馏水,及时带出排出的油和气体产物,对每份样品热模拟实验获得的油和气体产物进行收集和计量。As a preference, in the step 3, select representative large homogeneous mudstone samples, divide them into 9 parts and put them into the heating tank respectively, and do thermal evolution simulation experiments; 9 parts of samples are respectively heated from The experimental temperature is raised from room temperature to 250°C, 300°C, 350°C, 400°C, 450°C, 500°C, 550°C, 600°C, and 650°C. When each sample reaches its own end point temperature, use a constant The speed and constant flow pump injected distilled water at a rate of 2ml/min to take out the discharged oil and gas products in time, and collected and measured the oil and gas products obtained from the thermal simulation experiment of each sample.
作为优选,步骤三中,所述重质油产率和天然气产率演化模型如公式(9)和公式(10)所示,公式(9)和公式(10)的表达式如下:As a preference, in step 3, the heavy oil yield and natural gas yield evolution models are shown in formula (9) and formula (10), and the expressions of formula (9) and formula (10) are as follows:
单位有机质重质油产率=440.93VRo 3-1629VRo 2+2053.3VRo-618.7(9)Heavy oil yield per unit of organic matter=440.93VR o 3 -1629VR o 2 +2053.3VR o -618.7(9)
单位有机质天然气产率=18.371VRo 3+45.684VRo 2-62.693VRo+28.05(10)Unit organic matter natural gas yield = 18.371VR o 3 +45.684VR o 2 -62.693VR o +28.05(10)
式中,VRo为成熟度参数镜质体反射率。In the formula, VR o is the maturity parameter vitrinite reflectance.
作为优选,步骤三中,所述的实测成熟度参数镜质体反射率VRo随深度变化模型如公式(11)所示,公式(11)的表达式如下:As a preference, in step 3, the measured maturity parameter vitrinite reflectance VR o varies with depth as shown in formula (11), and the expression of formula (11) is as follows:
VRo=0.1605e0.535H(11)VR o =0.1605e 0.535H (11)
式中,H为样品点的埋藏深度,单位为:m。In the formula, H is the burial depth of the sample point in m.
作为优选,步骤四中,还根据步骤一和步骤二中获得的各个参数计算原始生烃潜量SOP及排烃系数KP,原始生烃潜量SOP、生烃量SGen、排烃量SExp及排烃系数KP的计算公式如公式(12)、(13)、(14)、(15)所示,公式(12)、(13)、(14)、(15)的表达式如下:Preferably, in step 4, the original hydrocarbon generation potential S OP and hydrocarbon expulsion coefficient K P are also calculated according to the parameters obtained in step 1 and step 2, the original hydrocarbon generation potential S OP , the amount of hydrocarbon generation S Gen , the hydrocarbon expulsion coefficient The calculation formulas of the amount S Exp and the hydrocarbon expulsion coefficient K P are shown in formulas (12), (13), (14), and (15), and the expressions of formulas (12), (13), (14), and (15) The formula is as follows:
SOP=TOC0×D0/0.083(12)S OP =TOC 0 ×D 0 /0.083(12)
SExp=SOP-(S1+S2)(13)S Exp = S OP - (S 1 +S 2 )(13)
SGen=SOP-S2(14)S Gen = S OP - S 2 (14)
KP=SExp/SGen×100%(15)K P = S Exp / S Gen × 100% (15)
式中,TOC0为原始有机碳,D0为原始降解率,S1为岩石Rock-Eval低温阶段热解获得的游In the formula, TOC 0 is the original organic carbon, D 0 is the original degradation rate, and S 1 is the free organic carbon obtained by pyrolysis in the rock-Eval low temperature stage.
离烃、S2为岩石Rock-Eval高温阶段热解获得的热解烃。The free hydrocarbons and S 2 are the pyrolyzed hydrocarbons obtained from the pyrolysis of rocks in the high temperature stage of Rock-Eval.
作为优选,步骤四中,通过公式(16)和公式(17)计算出每个深度点样品的油、气生成量,公式公式(16)和公式(17)的表达式如下:As a preference, in step 4, the oil and gas production amount of samples at each depth point is calculated by formula (16) and formula (17), and the expressions of formula (16) and formula (17) are as follows:
单位样品重质油生成量=单位有机质重质油产率×TOC(16)Production amount of heavy oil per unit sample = yield of heavy oil per unit of organic matter × TOC(16)
单位样品天然气生成量=□位有机□天然气产率×TOC(17)。The amount of natural gas generated per unit sample = □ organic □ natural gas yield × TOC (17).
作为优选,步骤四中,采用如公式(18)所示的热解生烃产率的差减法获得轻质油产率,公式(18)的表达式如下:As preferably, in step 4, the yield of light oil is obtained by subtracting the yield of pyrolysis hydrocarbon as shown in formula (18), and the expression of formula (18) is as follows:
Slo=SGen-Sho-Sg(18)S lo = S Gen - S ho - S g (18)
式中,Slo为轻质油产率,SGen为样品的原始生烃潜量,Sho为重质油产率,Sg为天然气产率。In the formula, S lo is the light oil yield, S Gen is the original hydrocarbon generation potential of the sample, S ho is the heavy oil yield, and S g is the natural gas yield.
本发明的有益效果是:(1)本发明首次建立不同有机碳形式的概念模型,将有机碳分为残留有机碳、残留有效碳、残留无效碳、排出有机碳、排出有效碳、原始有机碳、原始有效碳、原始无效碳,并建立了方法模型,可计算出这些各种形式的有机碳含量;本发明通过建立模型,能计算出非均质性评价泥页岩资源的各评价参数,包括原始生烃潜量SOP、生烃量SGen、排烃量SExp及排烃系数KP等;本发明还结合泥页岩中油气的油、气产率模型,进一步计算出泥页岩中的重质油量、轻质油量和天然气量;与常规的油气资源评价是用源岩体积平均化的方法估算不同,本方法模型是建立在每个样品点之上,可对泥页岩油气资源进行非均质性评价,对定量表征泥页岩含油气性的非均质性和准确评价非常规泥页岩油气资源有重要的意义。(2)本方案通过整体的一套参数进行泥页岩油气资源评价,如原始有机碳含量、原始生烃潜量、生烃量、排烃量、排烃系数、重质油产率、轻质油产率、天然气产率,本发明评价方法较以往单纯的评价泥页岩生烃量、或生油量、或生气量有重大的进步。(3)本方法可针对垂向大套泥页岩中的不同深度点同时进行计算,可评价泥页岩油气资源在垂向上的非均质性分布,其他的技术均是针对单个或有限的样品进行观测,不能反映泥页岩的非均质性。(4)本方法易操作可行,成本低,通过数据来源于Rock-Eval热解提供的残留有机碳含量、游离烃S1、热解烃S2、热解峰温Tmax、以及油、气产率模型即可进行计算;若样品有限,可利用密度测井、声波测井、电阻率测井信息预测残留有机碳含量,依据有限的实测样品可建立TOCRem和S2以及S1之间的相关性以及Tmax和深度的关系,这样就可以进一步根据测井数据预测的TOCRem值和相关性模型计算出对应的S2、S1以及Tmax值,即可完成整套方法计算,实现工业化泥页岩油气资源的整体评价。The beneficial effects of the present invention are: (1) the present invention establishes the conceptual model of different organic carbon forms for the first time, and organic carbon is divided into residual organic carbon, residual effective carbon, residual ineffective carbon, discharged organic carbon, discharged effective carbon, original organic carbon , original effective carbon, original invalid carbon, and established a method model, which can calculate these various forms of organic carbon content; the present invention can calculate each evaluation parameter of heterogeneity evaluation mud shale resources by establishing a model, Including the original hydrocarbon generation potential S OP , the amount of hydrocarbon generation S Gen , the amount of hydrocarbon expulsion S Exp and the coefficient of hydrocarbon expulsion K P , etc.; the present invention also combines the oil and gas yield models of oil and gas in mud shale to further calculate the mud sheet The amount of heavy oil, light oil and natural gas in rocks; different from conventional oil and gas resource evaluation, which uses source rock volume averaging method to estimate, this method model is established on each sample point, and can be used for mud The heterogeneity evaluation of shale oil and gas resources is of great significance to quantitatively characterize the heterogeneity of shale oil and gas and to accurately evaluate unconventional shale oil and gas resources. (2) This program evaluates shale oil and gas resources through a set of overall parameters, such as original organic carbon content, original hydrocarbon generation potential, hydrocarbon generation amount, hydrocarbon expulsion amount, hydrocarbon expulsion coefficient, heavy oil yield, light Quality oil yield, natural gas yield, the evaluation method of the present invention has significant progress compared with previous simple evaluation mud shale hydrocarbon generation amount, or oil generation amount, or gas generation amount. (3) This method can simultaneously calculate points at different depths in a large vertical set of shale, and can evaluate the heterogeneity distribution of shale oil and gas resources in the vertical direction. Other techniques are aimed at single or limited The samples were observed and could not reflect the heterogeneity of the shale. (4) This method is easy to operate, feasible, and low in cost. The data come from the residual organic carbon content provided by Rock-Eval pyrolysis, free hydrocarbon S 1 , pyrolysis hydrocarbon S 2 , pyrolysis peak temperature T max , and oil and gas The productivity model can be used for calculation; if the samples are limited, the residual organic carbon content can be predicted by using the density logging, acoustic logging, and resistivity logging information, and the relationship between TOC Rem and S 2 and S 1 can be established based on the limited measured samples. In this way, the corresponding S 2 , S 1 , and Tmax values can be calculated based on the TOC Rem value predicted by the logging data and the correlation model, and the calculation of the whole set of methods can be completed to realize the industrial mud Overall evaluation of shale oil and gas resources.
附图说明Description of drawings
附图1为本发明具体实施例通过Rock-Eval热解获得的TOCRem、S1、S2和Tmax值。Accompanying drawing 1 is the TOC Rem , S 1 , S 2 and T max values obtained by Rock-Eval pyrolysis in a specific embodiment of the present invention.
附图2为本发明具体实施例通过计算确定的每个深度样品点的氢指数HI、产率指数PI和烃指数[100×S1]/TOC。Accompanying drawing 2 is the hydrogen index HI, the yield index PI and the hydrocarbon index [100×S 1 ]/TOC of each deep sample point determined by calculation in a specific embodiment of the present invention.
附图3为本发明具体实施例氢指数HI与热解峰温Tmax的交汇图。Accompanying drawing 3 is the intersection chart of hydrogen index HI and pyrolysis peak temperature T max of the specific embodiment of the present invention.
附图4为本发明具体实施例有机碳不同形式划分的概念模型。Accompanying drawing 4 is the concept model of different forms of organic carbon division of the specific embodiment of the present invention.
附图5为本发明具体实施例有机碳形式划分与关系模型示意图。Accompanying drawing 5 is the schematic diagram of the division of the form of organic carbon and the relationship model of the specific embodiment of the present invention.
附图6为本发明具体实施例残留降解率DRem与热解峰温Tmax的交汇图。Accompanying drawing 6 is the intersection chart of residual degradation rate D Rem and pyrolysis peak temperature T max of the specific embodiment of the present invention.
附图7为本发明具体实施例各种形式有机碳含量的剖面分布图。Accompanying drawing 7 is the profile distribution figure of various forms of organic carbon content of specific embodiment of the present invention.
附图8为本发明具体实施例泥页岩生烃的评价参数剖面图。Accompanying drawing 8 is the sectional view of the evaluation parameters of mud shale hydrocarbon generation according to the specific embodiment of the present invention.
附图9为本发明具体实施例热演化模拟实验获得的重质油产率和天然气产率演化模型。Accompanying drawing 9 is the evolution model of heavy oil yield and natural gas yield obtained from the thermal evolution simulation experiment of the specific embodiment of the present invention.
附图10为本发明具体实施例每个单位样品点的重质油产率Sho、轻质油产率Slo、天然气产率Sg分布图。Figure 10 is a distribution diagram of heavy oil yield S ho , light oil yield S lo , and natural gas yield S g for each unit sample point in a specific embodiment of the present invention.
附图11为本发明具体实施例原油裂解成气模拟实验获得的原油裂解成气产率的变化模型。Accompanying drawing 11 is the variation model of the crude oil cracking gas production rate obtained from the crude oil cracking gas simulation experiment of the specific embodiment of the present invention.
附图12为本发明具体实施例东营凹陷古近系实测S2与TOCRem分段性相关性分布模型。Accompanying drawing 12 is the distribution model of segmental correlation between S2 and TOC Rem measured in Paleogene in Dongying depression according to a specific embodiment of the present invention.
附图13为本发明具体实施例东营凹陷古近系实测S1+S2与TOCRem分段性相关性分布模型。Accompanying drawing 13 is the distribution model of segmental correlation between S 1 +S 2 and TOC Rem measured in Paleogene in Dongying sag according to a specific embodiment of the present invention.
附图14为本发明具体实施例的流程框图。Accompanying drawing 14 is the flow chart diagram of the specific embodiment of the present invention.
图中,TOCRem:目前样品实测的残留有机碳,单位为%;TOC0:原始有机碳;TOCExp:排出有机碳,单位为%;TOCRea:热解转化成烃类的有效碳,单位为%;TOC0-rea:原始有效碳,单位为%;TOCRem-rea:残留有效碳,单位为%;TOCIne:不能热解转化成烃类的无效碳,单位为%;TOC0-ine:原始无效碳,单位为%;TOCRem-ine:残留无效碳,单位为%。In the figure, TOC Rem : residual organic carbon measured in the current sample, in %; TOC 0 : original organic carbon; TOC Exp : exhausted organic carbon, in %; TOC Rea : effective carbon converted into hydrocarbons by pyrolysis, in unit TOC 0-rea : original effective carbon, unit is %; TOC Rem-rea : residual effective carbon, unit is %; TOC Ine : invalid carbon that cannot be pyrolyzed into hydrocarbons, unit is %; TOC 0 -rea ine : original ineffective carbon, in %; TOC Rem-ine : residual ineffective carbon, in %.
具体实施方式detailed description
以下结合附图对本发明作进一步说明。The present invention will be further described below in conjunction with accompanying drawing.
本实施例渤海湾盆地东营N38井古近系沙河街组三段为例进行评价泥页岩生油气量的非均质性。In this example, the third member of Paleogene Shahejie Formation in Well N38 in Dongying, Bohai Bay Basin was taken as an example to evaluate the heterogeneity of oil and gas generation in mud shale.
如图14所示,一种非均质性评价泥页岩生油气量的方法,含有以下步骤:As shown in Fig. 14, a heterogeneity method for evaluating oil and gas generation of shale includes the following steps:
一、对泥页岩剖面上不同深度点密集采样,并通过Rock-Eval热解检测获取基本参数值,确定有机质类型。1. Intensively sample different depth points on the shale profile, and obtain basic parameter values through Rock-Eval pyrolysis detection to determine the type of organic matter.
在泥页岩剖面上深度方向每隔1-10m一个样品点进行采样,对采集的样品进行Rock-Eval热解分析,并通过Rock-Eval热解获得基本参数的参数值。本实施例中,所述的基本参数包括实测的残留有机碳TOCRem、岩石Rock-Eval低温阶段热解获得的游离烃S1、岩石Rock-Eval高温阶段热解获得的热解烃S2和热解峰温Tmax,其中,热解峰温Tmax为岩石Rock-Eval高温阶段热解获得的热解烃S2对应的峰值,实测的残留有机碳TOCRem为现今通过样品实际检测到的有机碳TOC,如图1所示为通过Rock-Eval热解获得的基础参数TOCRem、S1、S2和Tmax的参数值。根据基础参数确定每个深样品点的氢指数HI、产率指数PI和烃指数[100×S1]/TOC,如图2所示为确定的每个深度样品点的氢指数HI、产率指数PI和烃指数[100×S1]/TOC,其中,氢指数HI表示泥页岩的生烃潜力,产率指数PI表示泥页岩的成熟度和热演化。如图3所示为指数HI与热解峰温Tmax的交汇图,通过氢指数HI与热解峰温Tmax交汇图确定有机质类型,有机质类型分类采用目前石油工业常用的四分法:Ⅰ型、Ⅱ1型、Ⅱ2型和Ⅲ型。在实际操作中图1和图2中的每个样品点有机质类型通过图3确定。On the shale profile, samples are taken every 1-10m in the depth direction, and the collected samples are analyzed by Rock-Eval pyrolysis, and the parameter values of basic parameters are obtained through Rock-Eval pyrolysis. In this example, the basic parameters include the measured residual organic carbon TOC Rem , free hydrocarbons S 1 obtained from rock Rock-Eval low-temperature pyrolysis, pyrolyzed hydrocarbons S 2 obtained from rock Rock-Eval high-temperature pyrolysis, and The pyrolysis peak temperature T max , where the pyrolysis peak temperature T max is the peak value corresponding to the pyrolysis hydrocarbon S2 obtained by the pyrolysis of the rock Rock - Eval high temperature stage, and the measured residual organic carbon TOC Rem is actually detected by the samples today Organic carbon TOC, as shown in Figure 1, is the parameter values of the basic parameters TOC Rem , S 1 , S 2 and T max obtained by Rock-Eval pyrolysis. Determine the hydrogen index HI, yield index PI, and hydrocarbon index [100×S 1 ]/TOC of each deep sample point according to the basic parameters, as shown in Figure 2. The index PI and the hydrocarbon index [100×S 1 ]/TOC, where the hydrogen index HI indicates the hydrocarbon generation potential of the shale, and the productivity index PI indicates the maturity and thermal evolution of the shale. As shown in Figure 3, the intersection graph of the index HI and the pyrolysis peak temperature T max is used to determine the type of organic matter through the intersection graph of the hydrogen index HI and the pyrolysis peak temperature T max . Type, Type II1, Type II2 and Type III. In actual operation, the organic matter type of each sample point in Figure 1 and Figure 2 is determined through Figure 3.
二、建立概念模型并计算不同形式的有机碳含量。2. Establish a conceptual model and calculate the content of different forms of organic carbon.
根据有机碳的组成和转化原理,将泥页岩中有机碳分成不同有机碳形式的概念模型,如图4所示为有机碳不同形式划分的概念模型,将有机碳定义为残留有机碳、残留有效碳、残留无效碳、排出有机碳、排出有效碳、原始有机碳、原始有效碳、原始无效碳,泥页岩中总的原始有机碳TOC0包括排出有机碳TOCExp和残留有机碳TOCRem两部分,则存在关系式如公式(1)所示,在原始有机碳TOC0中,热解转化成烃类的有机碳部分定义为有效碳TOCrea,原始有机碳TOC0中所含有的有效碳和残留有机碳TOCRem中的有效碳分别定义为TOC0-rea和TOCRem-rea,如图5所示为有机碳形式划分与关系模型示意图。According to the composition and transformation principle of organic carbon, the conceptual model of organic carbon in mud shale is divided into different organic carbon forms, as shown in Figure 4. Available carbon, residual invalid carbon, expelled organic carbon, expelled available carbon, original organic carbon, original available carbon, original ineffective carbon, total original organic carbon TOC in mud shale 0 includes expelled organic carbon TOC Exp and residual organic carbon TOC Rem If there are two parts, there is a relationship as shown in formula (1). In the original organic carbon TOC 0 , the part of organic carbon converted into hydrocarbons by pyrolysis is defined as the effective carbon TOC rea , and the effective carbon contained in the original organic carbon TOC 0 Carbon and residual organic carbon The effective carbon in TOC Rem is defined as TOC 0-rea and TOC Rem-rea , respectively. Figure 5 is a schematic diagram of the division and relationship model of organic carbon.
所述公式(1)的表达式如下:The expression of described formula (1) is as follows:
TOC0=TOCRem+TOCExp(1)TOC 0 = TOC Rem +TOC Exp (1)
随着成熟度的增加,原始有机碳会逐渐转化成烃类,排出的有机碳含量会逐渐增加,残留的有机碳含量会逐渐减少。有效碳在有机质成熟度达到生油门限(即镜质体反射率Ro=0.5%)时,就开始转化成烃类,无效碳在无论多大热力时,均不能转化成烃类。With the increase of maturity, the original organic carbon will be gradually converted into hydrocarbons, the content of discharged organic carbon will gradually increase, and the content of residual organic carbon will gradually decrease. When the maturity of organic matter reaches the threshold of oil generation (ie vitrinite reflectance R o =0.5%), the available carbon will start to be converted into hydrocarbons, and the invalid carbon will not be converted into hydrocarbons no matter how much heat is applied.
泥页岩中残留的生烃潜力是由残留有机碳中的有效碳转化而来,它与残留有机碳TOCRem的残留降解率DRem存在的关系式如公式(2)所示;公式(2)的表达式如下:The residual hydrocarbon generation potential in mud shale is converted from the available carbon in the residual organic carbon, and the relationship between it and the residual degradation rate D Rem of residual organic carbon TOC Rem is shown in formula (2); formula (2 ) is expressed as follows:
DRem=TOCRem-rea/TOCRem(2)D Rem = TOC Rem-rea /TOC Rem (2)
目前石油工业中将0.083视为碳转化为烃类的转化系数,则存在关系式如公式(3)所示,公式(3)的表达式如下:At present, 0.083 is regarded as the conversion coefficient of carbon into hydrocarbons in the petroleum industry, then there is a relational expression as shown in formula (3), and the expression of formula (3) is as follows:
TOCRem-rea=(S1+S2)×0.083(3)TOC Rem-rea = (S 1 +S 2 )×0.083(3)
则残留降解率DRem由公式(4)计算获得,公式(4)的表达式如下:Then the residual degradation rate D Rem is calculated by the formula (4), and the expression of the formula (4) is as follows:
DRem=(S1+S2)×0.083/TOCRem(4)D Rem = (S 1 +S 2 )×0.083/TOC Rem (4)
如图6所示为残留降解率DRem与热解峰温Tmax的交汇图,根据残留降解率DRem和热解峰温Tmax的交汇图确定不同有机质的原始降解率D0。Figure 6 shows the intersection graph of the residual degradation rate D Rem and the pyrolysis peak temperature T max , and the original degradation rate D 0 of different organic matter is determined according to the intersection graph of the residual degradation rate D Rem and the pyrolysis peak temperature T max .
原始降解率D0由不同类型有机质的残留降解率DRem上线决定,也就是说,原始降解率D0是有机质成熟度非常低的时候的最大降解率。通过图6可以确定III、II2、II1和I的原始降解率D0分别为0.15、0.35、0.55、0.65。The original degradation rate D 0 is determined by the residual degradation rate D Rem of different types of organic matter, that is to say, the original degradation rate D 0 is the maximum degradation rate when the maturity of organic matter is very low. It can be determined from Fig. 6 that the original degradation rates D0 of III, II2, III1 and I are 0.15, 0.35, 0.55 and 0.65, respectively.
在有机质演化和成烃过程中,其中的无效碳可视为保持不变的,因此,存在关系式如公式(5)所示,公式(5)的表达式如下:In the process of organic matter evolution and hydrocarbon formation, the invalid carbon in it can be considered as constant, therefore, there is a relationship as shown in formula (5), and the expression of formula (5) is as follows:
TOC0(1–D0)=TOCRem(1–DRem)(5)TOC 0 (1–D 0 )=TOC Rem (1–D Rem )(5)
所述公式(5)中,TOC0(1–D0)代表原始有机质中的无效碳,定义为TOCIne,TOCRem(1–DRem)代表残留有机质中的无效碳,定义为TOCRem-Ine。In the formula (5), TOC 0 (1–D 0 ) represents the invalid carbon in the original organic matter, defined as TOC Ine , and TOC Rem (1–D Rem ) represents the invalid carbon in the residual organic matter, defined as TOC Rem- Ine .
由公式(5)可转化为公式(6)和公式(7),公式(6)和公式(7)的表达式如下:Formula (5) can be transformed into formula (6) and formula (7), and the expressions of formula (6) and formula (7) are as follows:
(1–DRem)/(1–D0)=TOC0/TOCRem(6)(1–D Rem )/(1–D 0 )=TOC 0 /TOC Rem (6)
RC=TOC0/TOCRem(7)R C =TOC 0 /TOC Rem (7)
所述公式(7)中,RC为现今测得的残留有机碳到原始有机碳的恢复系数,为常量系数,无单位。In the formula (7), R C is the recovery coefficient from the residual organic carbon to the original organic carbon measured today, which is a constant coefficient and has no unit.
同时,也存在关系式如公式(8)所示,公式(8)的表达式如下:At the same time, there is also a relational expression as shown in formula (8), and the expression of formula (8) is as follows:
TOC0–TOC0-rea=TOCRem–TOCRem-rea(8)TOC 0 -TOC 0-rea = TOC Rem -TOC Rem-rea (8)
所述公式(8)中,TOC0–TOC0-rea代表原始有机质中的无效碳,定义为TOC0-Ine,TOCRem–TOCRem-rea代表残留有机质中的无效碳,定义为TOCRem-Ine。In the formula (8), TOC 0 -TOC 0-rea represents the invalid carbon in the original organic matter, which is defined as TOC 0-Ine , and TOC Rem -TOC Rem-rea represents the invalid carbon in the residual organic matter, which is defined as TOC Rem- Ine .
通过以上公式计算出每个样品点的残留降解率DRem、原始有机碳恢复系数RC以及每种形式的有机碳含量在剖面的非均质性分布,为泥页岩油气资源评价提供基础数据,如图7所示为各种形式有机碳含量的剖面分布图。Calculate the residual degradation rate D Rem of each sample point, the original organic carbon recovery coefficient R C and the heterogeneity distribution of each form of organic carbon content in the profile through the above formula, and provide basic data for the evaluation of shale oil and gas resources , as shown in Figure 7, is the profile distribution diagram of various forms of organic carbon content.
三、设计模拟实验,建立重烃油产率和天然气产率演化模型。3. Design simulation experiments and establish evolution models of heavy hydrocarbon oil yield and natural gas yield.
选取具有代表性的大块均质泥岩样品,分成9份分别放进加热釜中,做热演化模拟实验;9份样品按50℃/h的速率,分别从实验温度由室温升温至250℃、300℃、350℃、400℃、450℃、500℃、550℃、600℃,650℃9个终点温度,在每份样品到达自己的终点温度时,用恒速恒流泵以2ml/min的速率注入蒸馏水,及时带出排出的油和气体产物,对每份样品热模拟实验获得的油和气体产物进行收集和计量,获取烃产率曲线。模拟产物根据分子量和物理性质分为三类,其一为相对大分子的重质油(即氯仿沥青“A”+排出重质油),可以直接获取;其二为小分子的气体(C1~C5),也可以直接获取;其三为常温下易挥发的C6~C14轻质油,实验中不易收集。以检测到的重质油和气体为依据,通过相互补偿的方法可以分析轻质油产率特征。实验中的实验温度可以根据埋藏史、热演化模型和生烃动力学转化成熟度参数镜质体反射率VRo。Select a representative large homogeneous mudstone sample, divide it into 9 parts and put them into the heating tank for thermal evolution simulation experiment; the 9 samples are raised from the experimental temperature from room temperature to 250 °C, 250 °C, 9 end temperatures of 300°C, 350°C, 400°C, 450°C, 500°C, 550°C, 600°C, and 650°C. When each sample reaches its end point temperature, use a constant-speed constant-flow pump at 2ml/min Inject distilled water at a high rate to take out the discharged oil and gas products in time, collect and measure the oil and gas products obtained from the thermal simulation experiment of each sample, and obtain the hydrocarbon yield curve. The simulated products are divided into three categories according to molecular weight and physical properties. One is heavy oil with relatively large molecules (that is, chloroform bitumen "A" + discharged heavy oil), which can be obtained directly; the other is gas with small molecules (C 1 ~C 5 ), which can also be obtained directly; the third is light oil of C 6 ~C 14 which is volatile at room temperature, which is not easy to collect in experiments. Based on the detected heavy oil and gas, the yield characteristics of light oil can be analyzed by means of mutual compensation. The experimental temperature in the experiment can be converted into the maturity parameter vitrinite reflectance VR o according to the burial history, thermal evolution model and hydrocarbon generation kinetics.
通过热演化模拟实验建立重质油产率和天然气产率演化模型,如图9所示为重质油产率和天然气产率演化模型,所述重质油产率和天然气产率演化模型如公式(9)和公式(10)所示,公式(9)和公式(10)的表达式如下:The heavy oil yield and natural gas yield evolution models were established through thermal evolution simulation experiments, as shown in Figure 9. The heavy oil yield and natural gas yield evolution models, the heavy oil yield and natural gas yield evolution models are as follows As shown in formula (9) and formula (10), the expressions of formula (9) and formula (10) are as follows:
单位有机质重质油产率=440.93VRo 3-1629VRo 2+2053.3VRo-618.7(9)Heavy oil yield per unit of organic matter=440.93VR o 3 -1629VR o 2 +2053.3VR o -618.7(9)
单位有机质天然气产率=18.371VRo 3+45.684VRo 2-62.693VRo+28.05(10)Unit organic matter natural gas yield = 18.371VR o 3 +45.684VR o 2 -62.693VR o +28.05(10)
式中,VRo为实测成熟度参数镜质体反射率。In the formula, VR o is the measured maturity parameter vitrinite reflectance.
建立实测成熟度参数镜质体反射率VRo随深度变化模型,该模型如公式(11)所示,公式(11)的表达式如下:Establish a model of the measured maturity parameter vitrinite reflectance VR o with depth, the model is shown in formula (11), and the expression of formula (11) is as follows:
VRo=0.1605e0.535H(11)VR o =0.1605e 0.535H (11)
式中,H为样品点的埋藏深度,单位为:m。In the formula, H is the burial depth of the sample point in m.
四、计算泥页岩不同深度点生成和排出的总烃量以及重质油量、轻质油量和生气量,评价泥页岩含油性和含气性的非均质性。4. Calculate the total hydrocarbons generated and discharged at different depth points of shale, as well as the amount of heavy oil, light oil and gas, and evaluate the heterogeneity of oil and gas content of shale.
根据上述步骤一和步骤二中获得的各个参数,计算每个泥页岩样品点单位原始生烃潜量SOP、总生烃量SGen、排烃量SExp及排烃系数KP,原始生烃潜量SOP、总生烃量SGen、排烃量SExp及排烃系数KP的计算公式如公式(12)、(13)、(14)、(15)所示,公式(12)、(13)、(14)、(15)的表达式如下:According to the parameters obtained in the above steps 1 and 2, calculate the unit original hydrocarbon generation potential S OP , total hydrocarbon generation S Gen , hydrocarbon expulsion S Exp and hydrocarbon expulsion coefficient K P for each shale sample point. The calculation formulas of hydrocarbon generation potential S OP , total hydrocarbon generation S Gen , hydrocarbon expulsion S Exp and hydrocarbon expulsion coefficient K P are shown in formulas (12), (13), (14), and (15). The formula ( The expressions of 12), (13), (14), and (15) are as follows:
SOP=TOC0×D0/0.083(12)S OP =TOC 0 ×D 0 /0.083(12)
SExp=SOP-(S1+S2)(13)S Exp = S OP - (S 1 +S 2 )(13)
SGen=SOP-S2(14)S Gen = S OP - S 2 (14)
KP=SExp/SGen×100%(15)K P = S Exp / S Gen × 100% (15)
式中,TOC0为原始有机碳,D0为原始降解率,S1为岩石Rock-Eval低温阶段热解获得的游离烃、S2为岩石Rock-Eval高温阶段热解获得的热解烃。In the formula, TOC 0 is the original organic carbon, D 0 is the original degradation rate, S 1 is the free hydrocarbons obtained from the pyrolysis of rocks in the low-temperature stage of Rock-Eval, and S 2 is the pyrolyzed hydrocarbons obtained in the pyrolysis of rocks in the high-temperature stage of Rock-Eval.
根据步骤三中建立的模型通过公式(16)和公式(17)计算出每个深度点样品的油、气生成量。公式(16)和公式(17)的表达式如下:According to the model established in step 3, the oil and gas generation of samples at each depth point are calculated through formula (16) and formula (17). The expressions of formula (16) and formula (17) are as follows:
单位样品重质油生成量=单位有机质重质油产率×TOC(16)Production amount of heavy oil per unit sample = yield of heavy oil per unit of organic matter × TOC(16)
单位样品天然气生成量=□位有机□天然气产率×TOC(17)Natural gas production per unit sample = □ organic □ natural gas yield × TOC(17)
在获取重质油、天然气产率后,进一步获取C6~C14轻质油产率,以检测到的重质油和气体为依据,通过相互补偿的方法可以获得轻质油产率,根据原始生烃潜量的组分分配,采用如公式(18)所示的热解生烃产率的差减法获得轻质油产率,公式(18)的表达式如下:After obtaining the yield of heavy oil and natural gas, the yield of C 6 ~C 14 light oil is further obtained. Based on the detected heavy oil and gas, the yield of light oil can be obtained by mutual compensation. According to For the component distribution of the original hydrocarbon generation potential, the light oil yield is obtained by subtracting the pyrolysis hydrocarbon generation yield as shown in formula (18). The expression of formula (18) is as follows:
Slo=SGen-Sho-Sg(18)S lo = S Gen - S ho - S g (18)
式中,Slo为轻质油产率,SGen为样品的原始生烃潜量,Sho为重质油产率,Sg为天然气产率。In the formula, S lo is the light oil yield, S Gen is the original hydrocarbon generation potential of the sample, S ho is the heavy oil yield, and S g is the natural gas yield.
通过上述模型获得每个单位样品点的重质油产率Sho、轻质油产率Slo、天然气产率Sg的分布,评价泥页岩含油性和含气性的非均质性。如图10所示为每个单位样品点的重质油产率Sho、轻质油产率Slo、天然气产率Sg分布图。The distribution of heavy oil yield S ho , light oil yield S lo , and natural gas yield S g of each unit sample point is obtained through the above model, and the heterogeneity of oil-bearing and gas-bearing properties of shale is evaluated. Figure 10 shows the distribution of heavy oil yield S ho , light oil yield S lo , and natural gas yield S g for each unit sample point.
根据获得的上述参数建立泥页岩生烃的评价参数剖面图,通过评价参数剖面图评价泥页岩油气资源剖面分布非均质性。According to the obtained above parameters, the evaluation parameter profile of shale hydrocarbon generation is established, and the profile distribution heterogeneity of shale oil and gas resources is evaluated through the evaluation parameter profile.
本实施例中的评价方法提供的渤海湾盆地东营N38井古近系沙河街组三段是在成熟度不是很高的情况下进行评价的。The third member of the Paleogene Shahejie Formation provided by the evaluation method in this example in the Dongying N38 well of the Bohai Bay Basin was evaluated when the maturity was not very high.
当成熟度很高时,会发生部分原油裂解成气,上述方案同样适用,只是多增加一个环节,根据原油裂解成气的产率,计算原油裂解成气的量。原油裂解成气的产率可根据模拟实验和原油裂解成气动力学,得出原油裂解成气的产率随成熟度参数VRo的变化。图11为根据原油裂解成气模拟实验获得的原油裂解成气产率的变化模型。具体方法,在现有文献中已有介绍,本发明不做详细介绍。When the maturity is very high, part of the crude oil will be cracked into gas. The above scheme is also applicable, but one more link is added. According to the yield of crude oil cracked into gas, the amount of crude oil cracked into gas will be calculated. The yield of crude oil cracked into gas can be obtained according to the simulation experiment and the dynamics of crude oil cracked into gas, and the change of the yield of crude oil cracked into gas with the maturity parameter VR o can be obtained. Fig. 11 is a variation model of the crude oil cracking gas production rate obtained according to the crude oil cracking gas simulation experiment. The specific method has been introduced in the existing literature, and the present invention does not introduce it in detail.
本实施例中提供的案例是根据大量实测样品获得的。当不具备大量样品时,亦可根据测井数据进行计算,因为测井数据具有高分辨率的特点,同时根据测井数据可以计算出关键参数有机碳含量,这里的有机碳含量是残留有机碳含量,具体方法很多,譬如说采用现在流行的Δlog法,本发明不做详细介绍。The cases provided in this embodiment are obtained based on a large number of measured samples. When a large number of samples are not available, it can also be calculated based on well logging data, because the well logging data has the characteristics of high resolution, and the key parameter organic carbon content can be calculated according to the well logging data, where the organic carbon content is the residual organic carbon content, there are many specific methods, for example, the popular Δlog method is adopted, which is not described in detail in the present invention.
残留有机碳TOCRem和热解参数S2和S1存在良好的相关性,因为三者能反映源岩的生烃潜力。依据有限的实测样品可建立TOCRem和S2以及S1+S2之间的相关性以及Tmax和深度的关系。TOCRem和S2以及S1+S2有时候采用分段进行相关性,效果更好。There is a good correlation between residual organic carbon TOC Rem and pyrolysis parameters S 2 and S 1 , because the three can reflect the hydrocarbon generation potential of source rocks. The correlation between TOC Rem and S 2 and S 1 +S 2 and the relationship between Tmax and depth can be established based on limited measured samples. TOC Rem and S 2 and S 1 + S 2 are sometimes correlated with segments, and the effect is better.
本实施例中,图12中表明,东营凹陷古近系实测S2与TOCRem分段性相关性分布:In this example, Figure 12 shows that the Paleogene measured S 2 and TOC Rem segmental correlation distribution in the Dongying sag:
当TOCRem<2时,S2=2.2441TOCRem 2-1.0291TOCRem+0.2697(R2=0.8947);When TOC Rem <2, S 2 =2.2441TOC Rem 2 -1.0291TOC Rem +0.2697 (R 2 =0.8947);
当2≤TOCRem<5时,S2=7.2813TOCRem-6.3066(R2=0.9348);When 2≤TOC Rem <5, S 2 =7.2813 TOC Rem -6.3066 (R 2 =0.9348);
当5≤TOCRem时,S2=3.9918TOCRem+10.424(R2=0.9809)。When 5≦TOC Rem , S 2 =3.9918 TOC Rem +10.424 (R 2 =0.9809).
本实施例中,图13中表明,东营凹陷古近系实测S1+S2与TOCRem分段性相关性分布:In this example, Figure 13 shows that the Paleogene measured S 1 +S 2 and TOC Rem segmental correlation distribution in Dongying sag:
当TOCRem<2时,S1+S2=2.8353TOCRem 2-1.6797TOCRem+0.4725(R2=0.8547)When TOC Rem <2, S 1 +S 2 =2.8353TOC Rem 2 -1.6797TOC Rem +0.4725(R 2 =0.8547)
当2≤TOCRem<5时,S1+S2=7.6804TOCRem-6.4302(R2=0.8274)When 2≤TOC Rem <5, S 1 +S 2 =7.6804TOC Rem -6.4302 (R 2 =0.8274)
当5≤TOCRem时,S1+S2=4.1906TOCRem+13.515(R2=0.9602)When 5≤TOC Rem , S 1 +S 2 =4.1906TOC Rem +13.515 (R 2 =0.9602)
这样就可以进一步根据测井数据预测的TOCRem值和相关性模型计算出对应的S2、S1以及Tmax值。其后面的计算即随本发明方法介绍相同。In this way, the corresponding S 2 , S 1 and Tmax values can be further calculated according to the TOC Rem value predicted by the logging data and the correlation model. Its subsequent calculation is the same as the introduction of the method of the present invention.
上述实施例用来解释本发明,而不是对本发明进行限制,在本发明的精神和权力要求的保护范围内,对本发明做出的任何修改和改变,都落入本发明的保护范围。The above-mentioned embodiments are used to explain the present invention, rather than to limit the present invention. Within the spirit of the present invention and the protection scope of the claims, any modification and change made to the present invention will fall into the protection scope of the present invention.
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