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CN113416531B - Composition of microbial-based viscosity-reducing fracturing fluid and its application - Google Patents

Composition of microbial-based viscosity-reducing fracturing fluid and its application Download PDF

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CN113416531B
CN113416531B CN202110663401.5A CN202110663401A CN113416531B CN 113416531 B CN113416531 B CN 113416531B CN 202110663401 A CN202110663401 A CN 202110663401A CN 113416531 B CN113416531 B CN 113416531B
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fracturing fluid
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翟怀建
董景锋
潘竟军
潘丽燕
王佳
任洪达
张敬春
罗腾
孙锡泽
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Abstract

本发明提供了一种微生物基降粘驱油压裂液组合物及其应用。该微生物基降粘驱油压裂液组合物包括:稠化剂、微生物、交联剂、破胶剂及水,微生物为枯草芽孢杆菌株,拉丁学名为Bacillus subtilis,保藏编号为CGMCC No.19809。稠化剂和交联剂能够通过交联作用形成具有特定结构和强度的高分子结构,在稠油开采过程中,能够对地层裂缝起到支撑作用。破胶剂可以对上述高分子结构进行破胶处理,从而使破胶液返排,同时减小稠油的流动阻力,起到提高稠油开采率的效果。上述特定的枯草芽孢杆菌株能够以稠油、稠化剂等作为碳源进行繁殖并分泌出降粘生物表面活性剂和小分子有机物,并大幅降低稠油的粘度,提高稠油采收率。

Figure 202110663401

The invention provides a microbial-based viscosity-reducing oil displacement fracturing fluid composition and application thereof. The microbial-based viscosity-reducing oil displacement fracturing fluid composition includes: thickener, microorganism, cross-linking agent, gel breaker and water. The microorganism is a strain of Bacillus subtilis, the Latin scientific name is Bacillus subtilis, and the preservation number is CGMCC No. 19809. Thickeners and cross-linking agents can form polymer structures with specific structure and strength through cross-linking, and can support formation fractures in the process of heavy oil production. The gel breaker can break the gel of the above polymer structure, so that the gel breaker can flow back, and at the same time reduce the flow resistance of the heavy oil, so as to improve the recovery rate of the heavy oil. The above-mentioned specific Bacillus subtilis strains can use heavy oil, thickener, etc. as carbon sources to reproduce and secrete viscosity-reducing biosurfactants and small molecular organics, which can greatly reduce the viscosity of heavy oil and improve heavy oil recovery.

Figure 202110663401

Description

微生物基降粘驱油压裂液组合物及其应用Composition of microbial-based viscosity-reducing fracturing fluid and its application

技术领域technical field

本发明涉及稠油开采领域,具体而言,涉及一种微生物基降粘驱油压裂液组合物及其应用。The invention relates to the field of heavy oil exploitation, in particular to a microbial-based viscosity-reducing oil displacement fracturing fluid composition and application thereof.

背景技术Background technique

稠油是一种多烃类混合物,其组成复杂,具有胶质、沥青质含量高,黏度高,密度大,流动性差等特点。目前,稠油开采的主要成熟技术是注蒸汽热采、火烧油层、热水与化学吞吐相结合、携砂冷采等,但均存在工艺复杂和成本高等问题。Heavy oil is a multi-hydrocarbon mixture with complex composition, high content of colloid and asphaltene, high viscosity, high density, and poor fluidity. At present, the main mature technologies for heavy oil recovery are thermal recovery with steam injection, oil layer combustion, combination of hot water and chemical huff and puff, cold recovery with sand, etc., but all of them have problems such as complex process and high cost.

水力压裂作为提高采收率的重要增产措施在稠油开发中应用范围不断增加,压裂液携带支撑剂泵入储层,形成高导流通道,能够有效提高稠油的采收率。稠油黏度较大,流动性差,压裂形成高导流通道的同时,要求压裂液能够降低稠油黏度、增加原油流动性、提高稠油采收率。压裂液降低稠油黏度的行之有效方法是添加稠油降粘剂,然而因压裂液注入油藏的量较少,能够波及到的体积较小,且随着压裂液的返排,稠油降粘效果持续时间较短。As an important stimulation measure to enhance oil recovery, hydraulic fracturing has been widely used in the development of heavy oil. The fracturing fluid carries proppant and is pumped into the reservoir to form high conductivity channels, which can effectively improve the oil recovery of heavy oil. Heavy oil has high viscosity and poor fluidity. While fracturing to form highly conductive channels, the fracturing fluid is required to reduce the viscosity of heavy oil, increase the fluidity of crude oil, and improve the recovery of heavy oil. The effective way for fracturing fluid to reduce the viscosity of heavy oil is to add heavy oil viscosity reducer. However, because the amount of fracturing fluid injected into the reservoir is small, the volume that can be swept is small, and with the flowback of fracturing fluid , the duration of the viscosity-reducing effect of heavy oil is short.

微生物稠油降粘法是指微生物利用碳源进行生长繁殖代谢,产生具有优异的稠油降粘、驱油功能的生物表面活性剂,使稠油快速乳化降粘,并促进石油在砂岩基质向井底流动,以达到提高油井产量的目的。微生物可利用稠油所含碳源生长繁殖及长期代谢生物表面活性剂,因此微生物降粘驱油作用持续效果较长。The microbial heavy oil viscosity reduction method refers to the use of carbon sources by microorganisms to grow, reproduce and metabolize to produce biosurfactants with excellent heavy oil viscosity reduction and oil displacement functions, so that the heavy oil can be quickly emulsified and reduced viscosity, and promote the oil to flow into the well in the sandstone matrix. Bottom flow to achieve the purpose of increasing oil well production. Microorganisms can use the carbon source contained in heavy oil to grow and reproduce and metabolize biosurfactants for a long time, so the effect of microbial viscosity reduction and displacement is longer.

现有文献提供了一种用于石油和天然气开采的新型水基压裂酶-微生物偶联压裂液体系,将水基压裂液中的化学助剂用具有相同作用的生物助剂替代,辅以加入外源微生物降解残渣、残胶作用,提高破胶效率,降低地层伤害。该压力液体系的作用原理为:采用生物酶破胶,将水基压裂液中的化学助剂用具有相同作用的生物助剂替代,辅以加入外源微生物降解残渣、残胶作用,提高破胶效率。The existing literature provides a new type of water-based fracturing enzyme-microbial coupling fracturing fluid system for oil and natural gas extraction, which replaces the chemical additives in the water-based fracturing fluid with biological additives with the same effect. Supplemented by the addition of exogenous microorganisms to degrade residues and residual glue, the gel breaking efficiency can be improved and formation damage can be reduced. The working principle of this pressure fluid system is: use biological enzymes to break the gel, replace the chemical additives in the water-based fracturing fluid with biological additives with the same effect, supplemented by adding exogenous microorganisms to degrade residues and residual glue, and improve Gel breaking efficiency.

另一篇现有文献提供了一种降低胍胶压裂液残渣的方法,将生物酶破胶剂加入胍胶压裂液中,该生物酶破胶剂在pH为7~14、温度为40~70℃范围内破胶,将交联胍胶降解为含有多糖、单糖和残渣的破胶液;将微生物革兰氏阴性杆菌加入到破胶液中,微生物革兰氏阴性杆菌以生物酶破胶液为营养源,在40~70℃,发酵24~48h,将破胶液和残渣转换成小分子物质,进一步降解生物酶未降解的残渣。该压力液体系的作用原理为:采用生物酶破胶,将交联胍胶降解为含有多糖、单糖和残渣的破胶液;将微生物革兰氏阴性杆菌加入到上述破胶液中,微生物革兰氏阴性杆菌以生物酶破胶液为营养源,将破胶液和残渣转换成小分子物质,进一步降解生物酶未降解的残渣。Another existing document provides a method for reducing the residue of guar gum fracturing fluid, adding a biological enzyme breaker into the guar gum fracturing fluid. The gel is broken in the range of ~70°C, and the cross-linked guar gum is degraded into a gel-breaking solution containing polysaccharides, monosaccharides and residues; microbial gram-negative bacilli are added to the gel-breaking solution, and the microbial gram-negative bacilli use enzymes to The gel-breaking solution is the nutrient source, and it is fermented at 40-70°C for 24-48 hours to convert the gel-breaking solution and residues into small molecular substances, and further degrade the residues not degraded by biological enzymes. The working principle of the pressure liquid system is: use biological enzymes to break the gel, degrade the cross-linked guar gum into a gel-breaking liquid containing polysaccharides, monosaccharides and residues; Gram-negative bacilli use the enzyme breaking solution as a nutrient source, convert the breaking solution and residue into small molecular substances, and further degrade the undegraded residue by the enzyme.

但是上述两种方法中均无法实现微生物的有效繁殖,因而上述两种胍胶压裂液均无法实现具有长效降粘、驱油作用。因而鉴于上述问题的存在,本领域亟需开发一种微生物基降粘驱油压裂液体系,以解决现有的压裂后化学降粘剂存在降粘作用持续时间短和作用效果有限的问题。However, the effective reproduction of microorganisms cannot be achieved in the above two methods, so the above two guar gum fracturing fluids cannot achieve long-term viscosity reduction and oil displacement. Therefore, in view of the existence of the above problems, there is an urgent need in the field to develop a microbial-based viscosity-reducing flooding fracturing fluid system to solve the problems of short duration and limited effect of the existing chemical viscosity-reducing agents after fracturing. .

发明内容Contents of the invention

本发明的主要目的在于提供一种微生物基降粘驱油压裂液组合物及其应用,以解决现有技术中的问题。The main purpose of the present invention is to provide a microbial-based viscosity-reducing oil displacement fracturing fluid composition and its application, so as to solve the problems in the prior art.

为了实现上述目的,本发明一方面提供了一种微生物基降粘驱油压裂液组合物,该微生物基降粘驱油压裂液组合物包括:稠化剂、微生物、交联剂、破胶剂及水,其中微生物为枯草芽孢杆菌株,拉丁学名为Bacillus subtilis,保藏编号为CGMCC No.19809。In order to achieve the above object, the present invention provides a microbial-based viscosity-reducing oil displacement fracturing fluid composition on the one hand, and the microbial-based viscosity-reducing oil displacement fracturing fluid composition includes: thickener, microorganism, crosslinking agent, Glue and water, wherein the microorganism is a strain of Bacillus subtilis, the Latin scientific name is Bacillus subtilis, and the preservation number is CGMCC No.19809.

进一步地,微生物以微生物菌液的形成中存在,优选地,微生物菌液中,枯草芽孢杆菌株的含量为1.0×107~1.0×1011CFU。Further, the microorganisms exist in the formation of microbial bacterial liquid, preferably, the content of the Bacillus subtilis strain in the microbial bacterial liquid is 1.0×10 7 -1.0×10 11 CFU.

进一步地,按重量份计,微生物基降粘驱油压裂液组合物包括:0.10~0.30份稠化剂、5~15份微生物菌液、0.10~0.20份交联剂和0.01~0.03份破胶剂,余量为水。Further, in parts by weight, the microbial-based viscosity-reducing oil displacement fracturing fluid composition includes: 0.10-0.30 parts of thickener, 5-15 parts of microbial bacterial liquid, 0.10-0.20 parts of cross-linking agent and 0.01-0.03 parts of breaking agent. Glue, the balance is water.

进一步地,微生物基降粘驱油压裂液组合物还包括粘土稳定剂和/或助排剂。Further, the microbial-based viscosity-reducing oil displacement fracturing fluid composition also includes a clay stabilizer and/or a drainage aid.

进一步地,按重量份计,微生物基降粘驱油压裂液组合物包括0~0.3份粘土稳定剂和0~0.3份助排剂。Further, the microbial-based viscosity-reducing oil displacement fracturing fluid composition includes 0-0.3 parts of clay stabilizer and 0-0.3 part of drainage aid in parts by weight.

进一步地,上述破胶剂为生物破胶剂。Further, the above-mentioned gel breaker is a biological gel breaker.

进一步地,稠化剂选自天然半乳甘露聚糖类化合物(胍胶、羟丙基胍胶、羧甲基羟丙基双衍生胍胶、羟丙基羧甲基胍胶)、聚丙烯酰胺类有机物、纤维素类稠化剂(羧甲基纤维素、羧乙基纤维素、羧甲基所病机纤维素)组成的组中的一种或多种。Further, the thickening agent is selected from natural galactomannan compounds (guar gum, hydroxypropyl guar gum, carboxymethyl hydroxypropyl bis-derived guar gum, hydroxypropyl carboxymethyl guar gum), polyacrylamide One or more of the group consisting of organic matter and cellulose thickener (carboxymethyl cellulose, carboxyethyl cellulose, carboxymethyl cellulose).

本申请另一方面还提供了一种本申请提供的微生物基降粘驱油压裂液组合物在稠油降粘体系中的应用。Another aspect of the present application also provides an application of the microbial-based viscosity-reducing oil displacement fracturing fluid composition provided in the present application in a heavy oil viscosity-reducing system.

进一步地,微生物基降粘驱油压裂液组合物添加量为20~30wt%。Further, the added amount of the microbial-based viscosity-reducing fracturing fluid composition is 20-30 wt%.

应用本发明的技术方案,稠化剂和交联剂能够通过交联作用形成具有特定结构和强度的高分子结构,在稠油开采过程中,能够对地层裂缝起到支撑作用。破胶剂可以对上述高分子结构进行破胶处理,从而使破胶液返排,同时减小稠油的流动阻力,起到提高稠油开采率的效果。上述特定的枯草芽孢杆菌株属于申请人获得的一种新的菌株,其能够以稠油、稠化剂等作为碳源进行繁殖并分泌出降粘生物表面活性剂和小分子有机物。且该生物表面活性剂能够大幅降低稠油的粘度(比如可使黏度为4400mPa·s稠油降至185mPa·s,降粘率达到95.8%),这能够解决地下稠油难以流动储层压裂改造后产量低及地面稠油管输、处理困难等难题。由于上述微生物能够在稠油中进行有效繁殖,并不断分泌出降粘生物表面活性剂,因而将本申请提供的微生物基降粘驱油压裂液组合物应用于稠油开采领域能够实现长期,且明显的降粘效果,因而本申请提供的微生物基降粘驱油压裂液组合物的研制对稠油开采领域具有非常好地推动作用,且具有较高的经济价值。By applying the technical scheme of the invention, the thickener and the crosslinking agent can form a polymer structure with specific structure and strength through crosslinking, and can support formation fractures during heavy oil production. The gel breaker can break the gel of the above polymer structure, so that the gel breaker can flow back, and at the same time reduce the flow resistance of the heavy oil, so as to improve the recovery rate of the heavy oil. The above-mentioned specific Bacillus subtilis strain belongs to a new strain obtained by the applicant, which can reproduce with heavy oil, thickener, etc. as carbon source and secrete viscosity-reducing biosurfactant and small molecular organic matter. Moreover, the biosurfactant can greatly reduce the viscosity of heavy oil (for example, it can reduce the viscosity of 4400mPa·s to 185mPa·s, and the viscosity reduction rate can reach 95.8%), which can solve the problem of fracturing in underground heavy oil that is difficult to flow. Problems such as low output after transformation and difficulties in ground heavy oil pipeline transportation and treatment. Since the above-mentioned microorganisms can effectively reproduce in heavy oil and continuously secrete viscosity-reducing biosurfactants, applying the microbial-based viscosity-reducing oil displacement fracturing fluid composition provided by the application to the field of heavy oil production can achieve long-term, And obvious viscosity-reducing effect, so the development of the microbial-based viscosity-reducing oil displacement fracturing fluid composition provided by the application has a very good role in promoting the field of heavy oil recovery, and has high economic value.

附图说明Description of drawings

构成本申请的一部分的说明书附图用来提供对本发明的进一步理解,本发明的示意性实施例及其说明用于解释本发明,并不构成对本发明的不当限定。在附图中:The accompanying drawings constituting a part of the present application are used to provide a further understanding of the present invention, and the schematic embodiments and descriptions of the present invention are used to explain the present invention, and do not constitute an improper limitation of the present invention. In the attached picture:

图1为对实施例中获得的微生物进行扫描电镜测试获得的电镜图;Fig. 1 is the electron micrograph that scanning electron microscope test is carried out to the microorganism that obtains in the embodiment;

图2为实施例1中在进行微生物基降黏驱油压裂液破胶液驱替前,对岩心进行扫描电镜测试获得的电镜图。Fig. 2 is an electron microscope image obtained by scanning electron microscope test on the core before the microbial-based viscosity-reducing flooding fracturing fluid gel-breaking fluid displacement in Example 1.

图3为实施例1中在进行微生物基降黏驱油压裂液破胶液驱替后,对岩心进行扫描电镜测试获得的电镜图。Fig. 3 is an electron microscope image obtained by scanning electron microscope test on the core after the microbial-based viscosity-reducing flooding fracturing fluid is displaced by gel-breaking fluid in Example 1.

本发明菌株的保藏信息Deposit information of the strain of the present invention

一种枯草芽孢杆菌株,该枯草芽孢杆菌株的拉丁学名为Bacillus subtilis,保藏于中国微生物菌种保藏管理委员会普通微生物中心,保藏地址为北京市朝阳区北辰路1号院3号,保藏日期为2020年5月12日,保藏编号为CGMCC No.19809。A strain of Bacillus subtilis, the Latin scientific name of which is Bacillus subtilis, is preserved in the General Microbiology Center of China Committee for the Collection of Microorganisms, and the preservation address is No. 3, No. 1, Beichen Road, Chaoyang District, Beijing, and the preservation date As of May 12, 2020, the deposit number is CGMCC No.19809.

具体实施方式Detailed ways

需要说明的是,在不冲突的情况下,本申请中的实施例及实施例中的特征可以相互组合。下面将结合实施例来详细说明本发明。It should be noted that, in the case of no conflict, the embodiments in the present application and the features in the embodiments can be combined with each other. The present invention will be described in detail below in conjunction with examples.

正如背景技术所描述的,现有的压裂后化学降粘剂存在降粘作用持续时间短和作用效果有限的问题。为了解决上述技术问题,本申请提供了一种微生物基降粘驱油压裂液组合物,微生物基降粘驱油压裂液组合物包括:稠化剂、微生物、交联剂、破胶剂及水,其中上述微生物为枯草芽孢杆菌株的拉丁学名为Bacillus subtilis,保藏编号为CGMCCNo.19809。As described in the background art, the existing chemical viscosity reducers after fracturing have the problems of short duration of viscosity reduction and limited effect. In order to solve the above technical problems, the present application provides a microbial-based viscosity-reducing oil displacement fracturing fluid composition, the microbial-based viscosity-reducing oil displacement fracturing fluid composition includes: thickener, microorganism, cross-linking agent, gel breaker And water, wherein the above-mentioned microorganism is Bacillus subtilis with a Latin scientific name of Bacillus subtilis, and the preservation number is CGMCC No.19809.

稠化剂和交联剂能够通过交联作用形成具有特定结构和强度的高分子结构,在稠油开采过程中,能够对地层裂缝起到支撑作用。破胶剂可以对上述高分子结构进行破胶处理,从而使破胶液返排,同时减小稠油的流动阻力,起到提高稠油开采率的效果。上述特定的枯草芽孢杆菌株属于申请人获得的一种新的菌株,其能够以稠油、稠化剂等作为碳源进行繁殖并分泌出降粘生物表面活性剂和小分子有机物。且该生物表面活性剂能够大幅降低稠油的粘度(比如可使黏度为4400mPa·s稠油降至185mPa·s,降粘率达到95.8%),这能够解决地下稠油难以流动储层压裂改造后产量低及地面稠油管输、处理困难等难题。由于上述微生物能够在稠油中进行有效繁殖,并不断分泌出降粘生物表面活性剂,因而将本申请提供的微生物基降粘驱油压裂液组合物应用于稠油开采领域能够实现长期,且明显的降粘效果,因而本申请提供的微生物基降粘驱油压裂液组合物的研制对稠油开采领域具有非常好地推动作用,且具有较高的经济价值。Thickeners and cross-linking agents can form polymer structures with specific structure and strength through cross-linking, and can support formation fractures in the process of heavy oil production. The gel breaker can break the gel of the above polymer structure, so that the gel breaker can flow back, and at the same time reduce the flow resistance of the heavy oil, so as to improve the recovery rate of the heavy oil. The above-mentioned specific Bacillus subtilis strain belongs to a new strain obtained by the applicant, which can reproduce with heavy oil, thickener, etc. as carbon source and secrete viscosity-reducing biosurfactant and small molecular organic matter. Moreover, the biosurfactant can greatly reduce the viscosity of heavy oil (for example, it can reduce the viscosity of 4400mPa·s to 185mPa·s, and the viscosity reduction rate can reach 95.8%), which can solve the problem of fracturing in underground heavy oil that is difficult to flow. Problems such as low output after transformation and difficulties in ground heavy oil pipeline transportation and treatment. Since the above-mentioned microorganisms can effectively reproduce in heavy oil and continuously secrete viscosity-reducing biosurfactants, applying the microbial-based viscosity-reducing oil displacement fracturing fluid composition provided by the application to the field of heavy oil production can achieve long-term, And obvious viscosity-reducing effect, so the development of the microbial-based viscosity-reducing oil displacement fracturing fluid composition provided by the application has a very good role in promoting the field of heavy oil recovery, and has high economic value.

在应用过程中,上述微生物(枯草芽孢杆菌株)以菌液的形式存在。比如在一种优选的实施例中,按5wt%的接种量将种子液加入到培养基中,并在35℃、170rpm下培养36h得到微生物菌液。During the application process, the above-mentioned microorganisms (Bacillus subtilis strain) exist in the form of bacterial liquid. For example, in a preferred embodiment, the seed solution is added to the culture medium at an inoculation amount of 5 wt%, and cultured at 35° C. and 170 rpm for 36 hours to obtain a microbial bacterial solution.

采用的培养基可以是本领域常用的组成。在一种优选的实施例中,上述培养基的组成为蔗糖12g/L,NH4Cl 1.5g/L,K2HPO4·12H2O 3.0g/L,KH2PO4 0.5g/L,NaCl 10g/L,FeSO4·7H2O0.015g/L,MnSO4 0.005g/L,CuSO4·5H2O 0.005g/L,pH 6.5。The culture medium used may be a composition commonly used in the art. In a preferred embodiment, the composition of the above medium is 12g/L sucrose, 1.5g/L NH 4 Cl, 3.0g/L K 2 HPO 4 ·12H 2 O, 0.5g/L KH 2 PO 4 , NaCl 10g/L, FeSO 4 ·7H 2 O 0.015g/L, MnSO 4 0.005g/L, CuSO 4 ·5H2O 0.005g/L, pH 6.5.

更优选地,上述微生物菌液中,微生物(枯草芽孢杆菌株)的含量为1.0×107~1.0×1011CFU。More preferably, the content of the microorganism (Bacillus subtilis strain) in the above microorganism liquid is 1.0×10 7 -1.0×10 11 CFU.

在微生物基降粘驱油压裂液组合物中加入上述特定的微生物能够使压裂液组合物具有持续和高效的降粘效果。为了更好地提高其降粘效果,需要对压裂组合物中的各组分的用量进行优化。在一种优选的实施例中,按重量份计,微生物基降粘驱油压裂液组合物包括:0.10~0.30份稠化剂、5~15份微生物菌液、0.10~0.20份交联剂和0.01~0.03份所述破胶剂,余量为水。上述几种组分的用量包括但不限于上述范围,而将其限定在上述范围内能使稠化剂与交联剂的交联作用,与微生物的降粘作用实现更好地协同增效作用,从而有利于进一步提高降粘和稠油增产提效的效果。Adding the above-mentioned specific microorganisms to the microbial-based viscosity-reducing oil displacement fracturing fluid composition can make the fracturing fluid composition have a sustained and efficient viscosity-reducing effect. In order to better improve its viscosity-reducing effect, it is necessary to optimize the dosage of each component in the fracturing composition. In a preferred embodiment, in parts by weight, the microbial-based viscosity-reducing oil displacement fracturing fluid composition includes: 0.10-0.30 parts of thickener, 5-15 parts of microbial bacterial liquid, 0.10-0.20 parts of cross-linking agent and 0.01 to 0.03 parts of the breaker, and the balance is water. The amount of the above-mentioned components includes but is not limited to the above-mentioned range, and limiting them within the above-mentioned range can make the cross-linking effect of the thickener and the cross-linking agent, and the viscosity-reducing effect of microorganisms achieve a better synergistic effect , which is conducive to further improving the effects of viscosity reduction and heavy oil production increase.

由于不同开采地层具有不同的地层结构和组成,因而为了进一步提高本申请提供的微生物基降粘驱油压裂液组合物在稠油开采过程中的实际效果,在一种优选的实施例中,微生物基降粘驱油压裂液组合物还包括粘土稳定剂和/或助排剂。Since different production formations have different formation structures and compositions, in order to further improve the actual effect of the microbial-based viscosity-reducing oil displacement fracturing fluid composition provided by the application in the heavy oil production process, in a preferred embodiment, The microbial-based viscosity reducing flooding fracturing fluid composition also includes clay stabilizers and/or drainage aids.

粘土稳定剂的加入能够抑制地层粘土膨胀和粘土微粒运移。助排剂的加入有利于提高压裂作用过程中的工作残液从地层从排出。更优选地,按重量份计,微生物基降粘驱油压裂液组合物包括0~0.3份粘土稳定剂、0~0.3份助排剂、0.01~0.03份生物酶破胶剂。The addition of clay stabilizer can inhibit formation clay swelling and clay particle migration. The addition of the drainage aid is beneficial to improve the discharge of the working residual fluid from the formation during the fracturing process. More preferably, in parts by weight, the microbial-based viscosity-reducing oil displacement fracturing fluid composition includes 0-0.3 parts of clay stabilizer, 0-0.3 part of drainage aid, and 0.01-0.03 part of bio-enzyme breaker.

上述微生物基降粘驱油压裂液组合物中,稠化剂、交联剂、粘土稳定剂、助排剂和破胶剂均可以采用本领域常用的种类。In the above microorganism-based viscosity-reducing oil displacement fracturing fluid composition, thickeners, crosslinking agents, clay stabilizers, drainage aids and gel breakers can all be of the types commonly used in the field.

可选地,稠化剂包括但不限于天然半乳甘露聚糖类化合物(胍胶、羟丙基胍胶、羧甲基羟丙基双衍生胍胶、羟丙基羧甲基胍胶)、聚丙烯酰胺类有机物、纤维素类稠化剂(羧甲基纤维素、羧乙基纤维素、羧甲基所病机纤维素)组成的组中的一种或多种。Optionally, thickeners include but are not limited to natural galactomannan compounds (guar gum, hydroxypropyl guar gum, carboxymethylhydroxypropyl bis-derivatized guar gum, hydroxypropyl carboxymethyl guar gum), One or more of the group consisting of polyacrylamide organic matter and cellulose thickener (carboxymethyl cellulose, carboxyethyl cellulose, carboxymethyl cellulose).

交联剂包括但不限于多聚环氧化合物pEPC、改性有机硼、亚甲基双丙烯酰胺中的一种或多种。上述破胶剂包括但不限于生物酶破胶剂(比如β-甘露聚糖酶等)。相比于化学破胶剂,生物酶破胶剂具有更加优异的破胶效果,且对地层的伤害更小。The crosslinking agent includes but not limited to one or more of polyepoxide pEPC, modified organoboron, and methylenebisacrylamide. The above-mentioned gel breakers include but are not limited to biological enzyme gel breakers (such as β-mannanase, etc.). Compared with chemical breakers, biological enzyme breakers have a better breaking effect and cause less damage to the formation.

本申请的另一方面还提供了一种优选的压裂液的制备方法:在搅拌条件下,将稠化剂(比如胍胶)加入水中,搅拌30min;加入微生物菌液搅拌均匀,选择性地添加粘土稳定剂、助排剂、破胶剂和交联剂,搅拌混合均匀形成所需的胍胶压裂液。Another aspect of the present application also provides a preferred method for preparing fracturing fluid: under stirring conditions, add a thickener (such as guar gum) to water, and stir for 30 minutes; add microbial bacterial liquid and stir evenly, selectively Add clay stabilizer, drainage aid, gel breaker and crosslinking agent, stir and mix evenly to form the required guar gum fracturing fluid.

本申请的又一方面还提供了一种本申请提供的微生物基降粘驱油压裂液组合物在稠油降粘体系中的应用。Another aspect of the present application also provides an application of the microbial-based viscosity-reducing oil displacement fracturing fluid composition provided in the present application in a heavy oil viscosity-reducing system.

由于本申请提供的微生物基降粘驱油压裂液组合物在稠油开采过程中具有长期、且稳定的降粘效果,因而将其应用在稠油开采领域对行业发展具有非常好地推动作用,且具有较高的经济价值。Since the microbial-based viscosity-reducing oil displacement fracturing fluid composition provided by this application has a long-term and stable viscosity-reducing effect in the process of heavy oil recovery, its application in the field of heavy oil recovery has a very good role in promoting the development of the industry , and has high economic value.

优选地,微生物基降粘驱油压裂液组合物添加量为20~30wt%。Preferably, the added amount of the microbial-based viscosity-reducing fracturing fluid composition is 20-30 wt%.

以下结合具体实施例对本申请作进一步详细描述,这些实施例不能理解为限制本申请所要求保护的范围。The present application will be described in further detail below in conjunction with specific examples, and these examples should not be construed as limiting the scope of protection claimed in the present application.

实施例中微生物菌种的培养过程:The cultivation process of microbial strain in the embodiment:

按5wt%的接种量将种子液加入到培养基中,并在35℃、170rpm下培养36h得到微生物菌液。上述培养基的组成为蔗糖12g/L,NH4Cl 1.5g/L,K2HPO4·12H2O 3.0g/L,KH2PO40.5g/L,NaCl 10g/L,FeSO4·7H2O 0.015g/L,MnSO4 0.005g/L,CuSO4·5H2O 0.005g/L,pH6.5。The seed solution was added to the culture medium at an inoculum amount of 5 wt%, and cultured at 35° C. and 170 rpm for 36 hours to obtain a microbial bacterial solution. The composition of the above medium is sucrose 12g/L, NH 4 Cl 1.5g/L, K 2 HPO 4 12H 2 O 3.0g/L, KH 2 PO 4 0.5g/L, NaCl 10g/L, FeSO 4 7H 2 O 0.015g/L, MnSO 4 0.005g/L, CuSO 4 ·5H2O 0.005g/L, pH 6.5.

经扫描电镜观察上述菌株的形态外观,如图1所示,其形态为杆菌,大小为(0.5~0.6)μm×(2~3)μm,无荚膜,周生鞭毛,可运动,初步鉴定为杆菌属。使用革兰氏染色鉴别细菌法进行鉴定,如图2所示,该结果显示菌株XJ-21为革兰氏阳性杆菌。The morphological appearance of the above-mentioned strain was observed by scanning electron microscope, as shown in Figure 1, its shape is a bacillus, the size is (0.5-0.6) μm × (2-3) μm, no capsule, perinatal flagella, mobile, preliminary identification For the genus Bacillus. Gram staining was used to identify bacteria, as shown in Figure 2, the results showed that strain XJ-21 was a Gram-positive bacillus.

对上述菌株进行16S rRNA基因序列分析,并根据16S rRNA基因测序结果进行系统进化分析,系统进化树见图3。分析结果显示菌株XJ-021与Bacillus subtilis NBRC101239的同源性最高。因而结合菌体形态观察和生理生化特征,鉴定为芽孢杆菌属的枯草芽孢杆菌。The 16S rRNA gene sequence analysis was carried out on the above strains, and the phylogenetic analysis was carried out according to the 16S rRNA gene sequencing results. The phylogenetic tree is shown in Figure 3. The analysis results showed that the strain XJ-021 had the highest homology with Bacillus subtilis NBRC101239. Therefore, combined with the morphological observation and physiological and biochemical characteristics of the bacteria, it was identified as Bacillus subtilis of the genus Bacillus.

压裂液体系的制备过程包括:在搅拌条件下,将稠化剂(比如胍胶)加入水中,搅拌30min;加入微生物菌液搅拌均匀,选择性地添加粘土稳定剂、助排剂、破胶剂和交联剂,搅拌混合均匀形成所需的胍胶压裂液。The preparation process of the fracturing fluid system includes: adding a thickener (such as guar gum) into water under stirring conditions, and stirring for 30 minutes; Agent and cross-linking agent, stir and mix evenly to form the required guar gum fracturing fluid.

实施例1Example 1

本实施例提供的一种微生物基降粘驱油压裂液体系,由微生物菌液、胍胶、压裂液助剂组成,以重量份数计,包括下列成分:稠化剂(羟丙基胍胶)0.10份、微生物菌液15份、交联剂(改性有机硼,克拉玛依市新聚工贸有限责任公司,XJ-03)0.10份、粘土稳定剂(有机季铵盐聚合物,克拉玛依市正诚有限责任公司,JN-1)0.3份、助排剂(鼠李糖脂)0.3份、生物酶破胶剂(β-甘露聚糖酶)0.01份,余量以水补足100份。A kind of microbial-based viscosity-reducing oil displacement fracturing fluid system provided in this embodiment is made up of microbial bacterial liquid, guar gum, and fracturing fluid auxiliary agent, and includes the following components in parts by weight: thickener (hydroxypropyl Guar gum) 0.10 parts, microbial bacterial liquid 15 parts, crosslinking agent (modified organic boron, Karamay Xinju Industry and Trade Co., Ltd., XJ-03) 0.10 parts, clay stabilizer (organic quaternary ammonium salt polymer, Karamay City Zhengcheng Co., Ltd., JN-1) 0.3 part, drainage aid (rhamnolipid) 0.3 part, biological enzyme gel breaker (β-mannanase) 0.01 part, and the balance was made up to 100 parts with water.

上述配制的压裂液破胶后得到压裂液破胶液,对破胶液的稠油降粘性能、驱油性能开展测试。After the above prepared fracturing fluid is broken, the fracturing fluid breaker is obtained, and the thick oil viscosity reduction performance and oil displacement performance of the breaker are tested.

(1)破胶液降粘性能测试(1) Viscosity reduction performance test of gel breaking fluid

取30g破胶液加入70g脱水稠油(稠油来源为新疆油田吉7井区)内,摇晃均匀,置于60℃烘箱,测定原油前后粘度变化。Take 30g of gel-breaking solution and add it to 70g of dehydrated heavy oil (the source of heavy oil is Ji 7 well area of Xinjiang Oilfield), shake evenly, put it in a 60°C oven, and measure the viscosity change of crude oil before and after.

2天后,稠油黏度由4400mPa·s降至620mPa·s,降粘率为85.9%;6天后,稠油黏度由4400mPa·s降至188mPa·s,降粘率为95.8%。After 2 days, the viscosity of the heavy oil decreased from 4400mPa·s to 620mPa·s, and the viscosity reduction rate was 85.9%. After 6 days, the viscosity of the heavy oil decreased from 4400mPa·s to 188mPa·s, and the viscosity reduction rate was 95.8%.

(2)破胶液驱油性能测试(2) Oil displacement performance test of gel breaking fluid

岩心驱替实验:将标准天然岩心置于105℃烘箱烘干,使用粘度为1.5mPa·s的原油建立饱和油后分别进行驱替实验。将配制好的模拟地层水装入中间容器,驱替饱和油的岩心直至不出油,读取油水分离器的刻度,计算原油采出程度;破胶液装入中间容器,驱替水驱后的岩心(10PV),记录第1次采油量;关闭岩心前后端阀门,保持围压为2MPa,在夹持器中孵育2d;用模拟地层水驱至不出油为止,记录第二次采油量;二次采油量之和为总采油量,根据总采油量计算最终采出程度。岩心驱替实验的最终采收率为64.41%,其中水驱油率为49.3%,破胶液驱油率为15.11%。Core displacement experiments: standard natural cores were dried in an oven at 105°C, and crude oil with a viscosity of 1.5mPa·s was used to establish saturated oil, and then displacement experiments were carried out. Put the prepared simulated formation water into the intermediate container, displace the oil-saturated core until no oil comes out, read the scale of the oil-water separator, and calculate the degree of crude oil recovery; record the first oil recovery; close the front and rear valves of the core, keep the confining pressure at 2 MPa, and incubate in the holder for 2 days; flood with simulated formation water until no oil comes out, and record the second oil recovery ; The sum of the secondary oil recovery is the total oil recovery, and the final recovery degree is calculated according to the total oil recovery. The ultimate recovery rate of the core displacement experiment is 64.41%, among which the water flooding rate is 49.3%, and the gel-breaking fluid flooding rate is 15.11%.

(3)对微生物基降黏驱油压裂液破胶液驱替前后的岩心进行扫描电镜测试。(3) The scanning electron microscope test was carried out on the cores before and after displacement by the microbial-based viscosity-reducing fracturing fluid and the gel-breaking fluid.

观察驱替前后岩心状态变化。图2表示驱替之前的电镜图,图3为驱替后的电镜图。由图3中矩形区域可以清楚地看到发现岩心孔隙中存在的杆状菌体,微生物在驱替后的岩心中有生长及繁殖现象,说明压裂液内的微生物可以进入岩心进行生长并代谢产生活性物质。Observe the change of core state before and after displacement. Fig. 2 shows the electron micrograph before displacement, and Fig. 3 is the electron micrograph after displacement. From the rectangular area in Figure 3, it can be clearly seen that rod-shaped bacteria exist in the pores of the core, and the microorganisms have grown and reproduced in the core after displacement, indicating that the microorganisms in the fracturing fluid can enter the core to grow and metabolize produce active substances.

实施例2Example 2

本实施例提供的一种微生物基降粘驱油压裂液体系,由微生物菌液、胍胶、压裂液助剂及交联剂组成,以重量份数计,包括下列成分:A microbial-based viscosity-reducing oil displacement fracturing fluid system provided in this embodiment is composed of microbial bacterial fluid, guar gum, fracturing fluid auxiliary agent and crosslinking agent, and includes the following components in parts by weight:

稠化剂(羟丙基胍胶)0.20份、微生物菌液(XJ-21发酵液)10份、交联剂(改性有机硼,克拉玛依市新聚工贸有限责任公司,XJ-03)0.10份、粘土稳定剂(有机季铵盐聚合物,厂家克拉玛依市正诚有限责任公司,JN-1)0.3份、助排剂(鼠李糖脂)0.3份、生物酶破胶剂(β-甘露聚糖酶)0.01份,余量以水补足100份。Thickener (hydroxypropyl guar gum) 0.20 parts, microbial bacterial liquid (XJ-21 fermentation liquid) 10 parts, crosslinking agent (modified organic boron, Karamay Xinju Industry and Trade Co., Ltd., XJ-03) 0.10 parts 0.3 parts, clay stabilizer (organic quaternary ammonium salt polymer, manufacturer Karamay Zhengcheng Co., Ltd., JN-1) 0.3 parts, drainage aid (rhamnolipid) 0.3 parts, biological enzyme gel breaker (β-mannose Glycanase) 0.01 part, and the balance is made up to 100 parts with water.

上述配制的压裂液破胶后得到压裂液破胶液,对破胶液的稠油降粘性能、驱油性能开展测试。After the above prepared fracturing fluid is broken, the fracturing fluid breaker is obtained, and the thick oil viscosity reduction performance and oil displacement performance of the breaker are tested.

(1)破胶液降粘性能测试(1) Viscosity reduction performance test of gel breaking fluid

测试具体过程同实施例1。Test specific process with embodiment 1.

2天后,稠油黏度由4400mPa·s降至612mPa·s,降粘率为86.1%;6天后,稠油黏度由4400mPa·s降至183mPa·s,降粘率为95.8%。After 2 days, the viscosity of the heavy oil decreased from 4400mPa·s to 612mPa·s, and the viscosity reduction rate was 86.1%. After 6 days, the viscosity of the heavy oil decreased from 4400mPa·s to 183mPa·s, and the viscosity reduction rate was 95.8%.

(2)破胶液驱油性能测试(2) Oil displacement performance test of gel breaking fluid

岩心驱替实验:具体过程同实施例1。Core displacement experiment: the specific process is the same as in Example 1.

岩心驱替实验的最终采收率为62.76%,其中水驱油率为47.59%,破胶液驱油率为15.17%。The ultimate recovery rate of the core displacement experiment is 62.76%, among which the water flooding rate is 47.59%, and the gel-breaking fluid flooding rate is 15.17%.

实施例3Example 3

本实施例提供的一种微生物基降粘驱油压裂液体系,由微生物菌液、胍胶、压裂液助剂及交联剂组成,以重量份数计,包括下列成分:A microbial-based viscosity-reducing oil displacement fracturing fluid system provided in this embodiment is composed of microbial bacterial fluid, guar gum, fracturing fluid auxiliary agent and crosslinking agent, and includes the following components in parts by weight:

稠化剂(羟丙基胍胶)0.30份、微生物菌液(XJ-21发酵液)5份、交联剂(改性有机硼,克拉玛依市新聚工贸有限责任公司,XJ-03)0.20份、粘土稳定剂(有机季铵盐聚合物,克拉玛依市正诚有限责任公司,JN-1)0.3份、助排剂(鼠李糖脂)0.3份、生物酶破胶剂(β-甘露聚糖酶)0.01份,余量以水补足100份。Thickener (hydroxypropyl guar gum) 0.30 parts, microbial bacterial liquid (XJ-21 fermentation liquid) 5 parts, crosslinking agent (modified organic boron, Karamay Xinju Industry and Trade Co., Ltd., XJ-03) 0.20 0.3 part, clay stabilizer (organic quaternary ammonium salt polymer, Karamay Zhengcheng Co., Ltd., JN-1) 0.3 part, drainage aid (rhamnolipid) 0.3 part, biological enzyme gel breaker (β-mannan carbohydrase) 0.01 part, and the balance is made up to 100 parts with water.

上述配制的压裂液破胶后得到压裂液破胶液,对破胶液的稠油降粘性能、驱油性能开展测试。After the above prepared fracturing fluid is broken, the fracturing fluid breaker is obtained, and the thick oil viscosity reduction performance and oil displacement performance of the breaker are tested.

(1)破胶液降粘性能测试(1) Viscosity reduction performance test of gel breaking fluid

测试具体过程同实施例1。Test specific process with embodiment 1.

2天后,稠油黏度由4400mPa·s降至723mPa·s,降粘率为83.6%;6天后,稠油黏度由4400mPa·s降至199mPa·s,降粘率为95.5%。After 2 days, the viscosity of the heavy oil decreased from 4400mPa·s to 723mPa·s, and the viscosity reduction rate was 83.6%. After 6 days, the viscosity of the heavy oil decreased from 4400mPa·s to 199mPa·s, and the viscosity reduction rate was 95.5%.

(2)破胶液驱油性能测试(2) Oil displacement performance test of gel breaking fluid

岩心驱替实验:具体过程同实施例1。Core displacement experiment: the specific process is the same as in Example 1.

岩心驱替实验的最终采收率为64.55%,其中水驱油率为48.25%,破胶液驱油率为16.3%。The ultimate recovery rate of the core displacement experiment is 64.55%, among which the water flooding rate is 48.25%, and the gel-breaking fluid flooding rate is 16.3%.

实施例4Example 4

本实施例提供的一种微生物基降粘驱油压裂液体系,由微生物菌液、胍胶、压裂液助剂及交联剂组成,以重量份数计,包括下列成分:A microbial-based viscosity-reducing oil displacement fracturing fluid system provided in this embodiment is composed of microbial bacterial fluid, guar gum, fracturing fluid auxiliary agent and crosslinking agent, and includes the following components in parts by weight:

稠化剂(羟丙基胍胶)0.20份、微生物菌液(XJ-21发酵液)2份、交联剂(改性有机硼,克拉玛依市新聚工贸有限责任公司,XJ-03)0.10份、粘土稳定剂(有机季铵盐聚合物,克拉玛依市正诚有限责任公司,JN-1)0.3份、助排剂(鼠李糖脂)0.3份、生物酶破胶剂(β-甘露聚糖酶)0.01份,余量以水补足100份。Thickener (hydroxypropyl guar gum) 0.20 parts, microbial bacterial liquid (XJ-21 fermentation liquid) 2 parts, crosslinking agent (modified organic boron, Karamay Xinju Industry and Trade Co., Ltd., XJ-03) 0.10 0.3 part, clay stabilizer (organic quaternary ammonium salt polymer, Karamay Zhengcheng Co., Ltd., JN-1) 0.3 part, drainage aid (rhamnolipid) 0.3 part, biological enzyme gel breaker (β-mannan carbohydrase) 0.01 part, and the balance is made up to 100 parts with water.

上述配制的压裂液破胶后得到压裂液破胶液,对破胶液的稠油降粘性能、驱油性能开展测试。After the above prepared fracturing fluid is broken, the fracturing fluid breaker is obtained, and the thick oil viscosity reduction performance and oil displacement performance of the breaker are tested.

(1)破胶液降粘性能测试(1) Viscosity reduction performance test of gel breaking fluid

测试具体过程同实施例1。Test specific process with embodiment 1.

2天后,稠油黏度由4400mPa·s降至2300mPa·s,降粘率47.73%;6天后,稠油黏度由4400mPa·s降至430mPa·s,降粘率为90.23%。After 2 days, the viscosity of the heavy oil decreased from 4400mPa·s to 2300mPa·s, and the viscosity reduction rate was 47.73%. After 6 days, the viscosity of the heavy oil decreased from 4400mPa·s to 430mPa·s, and the viscosity reduction rate was 90.23%.

(2)破胶液驱油性能测试(2) Oil displacement performance test of gel breaking fluid

岩心驱替实验:具体过程同实施例1。Core displacement experiment: the specific process is the same as in Example 1.

岩心驱替实验的最终采收率为58.75%,其中水驱油率为48.25%,破胶液驱油率为10.5%。The ultimate recovery rate of the core displacement experiment is 58.75%, among which the water flooding rate is 48.25%, and the gel-breaking fluid flooding rate is 10.5%.

实施例5Example 5

与实施例2的区别为:没有加入上述粘土稳定剂、助排剂和生物酶破胶剂。The difference from Example 2 is that the above-mentioned clay stabilizer, drainage aid and bio-enzyme breaker are not added.

(1)破胶液降粘性能测试(1) Viscosity reduction performance test of gel breaking fluid

测试具体过程同实施例1。Test specific process with embodiment 1.

2天后,稠油黏度由4400mPa·s降至2750mPa·s,降粘率37.5%;6天后,稠油黏度由4400mPa·s降至740mPa·s,降粘率为83.18%。After 2 days, the viscosity of the heavy oil decreased from 4400mPa·s to 2750mPa·s, with a viscosity reduction rate of 37.5%. After 6 days, the viscosity of the heavy oil decreased from 4400mPa·s to 740mPa·s, with a viscosity reduction rate of 83.18%.

(2)破胶液驱油性能测试(2) Oil displacement performance test of gel breaking fluid

岩心驱替实验:具体过程同实施例1。Core displacement experiment: the specific process is the same as in Example 1.

岩心驱替实验的最终采收率为58.15%,其中水驱油率为47.92%,破胶液驱油率为10.23%。The ultimate recovery rate of the core displacement experiment is 58.15%, among which the water flooding rate is 47.92%, and the gel-breaking fluid flooding rate is 10.23%.

对比例1Comparative example 1

与实施例2的区别为:没有加入上述微生物菌液。The difference from Example 2 is that the above-mentioned microbial bacterial liquid is not added.

(1)破胶液降粘性能测试(1) Viscosity reduction performance test of gel breaking fluid

测试具体过程同实施例1。Test specific process with embodiment 1.

2天后,稠油黏度由4400mPa·s降至3150mPa·s,降粘率28.41%;6天后,稠油黏度由4400mPa·s降至2670mPa·s,降粘率为39.32%。After 2 days, the viscosity of the heavy oil decreased from 4400mPa·s to 3150mPa·s, with a viscosity reduction rate of 28.41%. After 6 days, the viscosity of the heavy oil decreased from 4400mPa·s to 2670mPa·s, with a viscosity reduction rate of 39.32%.

(2)破胶液驱油性能测试(2) Oil displacement performance test of gel breaking fluid

岩心驱替实验:具体过程同实施例1。Core displacement experiment: the specific process is the same as in Example 1.

岩心驱替实验的最终采收率为52.04%,其中水驱油率为48.13%,破胶液驱油率为3.91%。The ultimate recovery rate of the core displacement experiment is 52.04%, among which the water flooding rate is 48.13%, and the gel-breaking fluid flooding rate is 3.91%.

从以上的描述中,可以看出,本发明上述的实施例实现了如下技术效果:相比于现有的驱油组合物,将本申请提供的微生物基降粘驱油压裂液组合物应用于稠油开采领域具有较为明显的降粘效果,同时还有利于大幅提高稠油采收率。From the above description, it can be seen that the above-mentioned embodiments of the present invention have achieved the following technical effects: compared with the existing oil displacement composition, the application of the microbial-based viscosity-reducing oil displacement fracturing fluid composition provided by the application It has obvious viscosity-reducing effect in the field of heavy oil production, and it is also conducive to greatly improving heavy oil recovery.

需要说明的是,本申请的说明书和权利要求书中的术语“第一”、“第二”等是用于区别类似的对象,而不必用于描述特定的顺序或先后次序。应该理解这样使用的术语在适当情况下可以互换,以便这里描述的本申请的实施方式例如能够以除了在这里描述的那些以外的顺序实施。It should be noted that the terms "first" and "second" in the specification and claims of the present application are used to distinguish similar objects, but not necessarily used to describe a specific order or sequence. It is to be understood that the terms so used are interchangeable under appropriate circumstances such that the embodiments of the application described herein are, for example, capable of operation in sequences other than those described herein.

以上所述仅为本发明的优选实施例而已,并不用于限制本发明,对于本领域的技术人员来说,本发明可以有各种更改和变化。凡在本发明的精神和原则之内,所作的任何修改、等同替换、改进等,均应包含在本发明的保护范围之内。The above descriptions are only preferred embodiments of the present invention, and are not intended to limit the present invention. For those skilled in the art, the present invention may have various modifications and changes. Any modifications, equivalent replacements, improvements, etc. made within the spirit and principles of the present invention shall be included within the protection scope of the present invention.

Claims (3)

1. The microbial-based viscosity-reducing oil-displacing fracturing fluid composition is characterized by comprising the following components in parts by weight: 0.10-0.30 part of thickening agent, 5-15 parts of microorganism, 0.10-0.20 part of cross-linking agent, 0.01-0.03 part of gel breaker, 0-0.3 part of clay stabilizer, 0-0.3 part of cleanup additive and the balance of water, wherein the dosage of the clay stabilizer and the dosage of the cleanup additive are not 0, the microorganism is Bacillus subtilis strain, the Latin is Bacillus subtilis, and the preservation number is CGMCC No.19809; the microorganism exists in the form of microorganism liquid, and the content of bacillus subtilis strain in the microorganism liquid is 1.0 multiplied by 10 7 ~1.0×10 11 A CFU; the thickening agent is selected from hydroxypropyl guar gum; the gel breaker is selected from beta-mannanase.
2. The application of the microorganism-based viscosity-reducing oil-displacing fracturing fluid composition of claim 1 in a viscous oil viscosity-reducing system.
3. The application of the microbial-based viscosity-reducing, oil-displacing and fracturing fluid composition in a thick oil viscosity-reducing system according to claim 2, wherein the addition amount of the microbial-based viscosity-reducing, oil-displacing and fracturing fluid composition is 20-30 wt%.
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