WO2018108186A1 - 一种兼具洗油作用的自生酸诱导增粘调控体系及制备方法 - Google Patents

一种兼具洗油作用的自生酸诱导增粘调控体系及制备方法 Download PDF

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WO2018108186A1
WO2018108186A1 PCT/CN2017/119361 CN2017119361W WO2018108186A1 WO 2018108186 A1 WO2018108186 A1 WO 2018108186A1 CN 2017119361 W CN2017119361 W CN 2017119361W WO 2018108186 A1 WO2018108186 A1 WO 2018108186A1
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acid
oil
induced viscosity
control system
induced
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French (fr)
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赵光
戴彩丽
由庆
谷成林
吕亚慧
张跃
孙永鹏
方吉超
刘逸飞
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中国石油大学(华东)
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    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
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    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/58Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids
    • C09K8/584Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids characterised by the use of specific surfactants
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/58Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids
    • C09K8/588Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids characterised by the use of specific polymers

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  • the invention belongs to the field of oilfield chemistry, and in particular relates to a self-generated acid induced viscosity-increasing regulation system and a preparation method thereof for washing oil in a medium-low temperature oil reservoir.
  • CN86108877 discloses a zirconium jelly water shutoff control agent consisting of polyacrylamide (PAM) or methylidene polyacrylamide (MPAM) and a crosslinker inorganic zirconium compound.
  • the inorganic zirconium compound is zirconium oxychloride, zirconium tetrachloride, zirconium sulfate, zirconium nitrate or the like.
  • the zirconium jelly regulator can meet the water blockage of the temperature below 70 °C.
  • the solution and the cross-linking agent inorganic zirconium compound are injected alternately, which increases the construction process of the mine, and the zirconium jelly control system is formed into a rapid gel, and there is a certain engineering risk in the construction process.
  • the reservoir regulators currently developed mainly improve the oil recovery rate by increasing the sweep coefficient of the oil displacing agent, and less on the oil washing efficiency of the reservoir regulator itself.
  • CN103254883A discloses an oil displacing agent for improving oil recovery rate of high temperature, high salt and high hardness oil reservoir, which is composed of an amine oxide type amphoteric surfactant and an alkylphenol ethoxylate ether carboxylic acid surfactant, which can reduce oil and water.
  • the interface tension is 10 -2 mN/m.
  • the oil displacement system is suitable for relatively homogeneous formations. For high-water heterogeneous reservoirs with percolation dominant channels, the fluidity of the injected oil displacing agent can not be well controlled when used alone, and it is easy to refer along the high permeability layer. , reducing the oil displacement effect.
  • the present invention provides a symbiotic acid-induced viscosity-increasing control system and a preparation method thereof for use in a medium-low temperature oil reservoir.
  • the initial stage of the system has the ability to reduce the oil-water interfacial tension and improve the oil washing efficiency. After the viscosity is increased, the deep regulation of the formation can be realized to expand the volume of the mixture.
  • the present invention adopts the following scheme:
  • a self-generated acid-induced viscosity-increasing regulation system with oil washing effect comprising: anionic polymer, sodium alkyl sulfate surfactant, methyl propylene diamine, slow-speed acid, reinforcing agent and liquid water, quality component as follows:
  • the balance is the liquid water, and the sum of the mass fractions of the components is 100%.
  • the anionic polymer has a molecular weight of 10 million to 12 million and a degree of hydrolysis of 20 to 25%.
  • the sodium alkyl sulfate has the structural formula:
  • n is an alkyl group having a sum of 10 to 14, preferably 11;
  • M is a metal ion, preferably sodium;
  • the methyl propylene diamine has the structural formula:
  • n is from 1 to 3, preferably 2.
  • the slow-speed acid is a polyvinyl chloride powder, and the particle size is distributed between 1 and 5 ⁇ m.
  • the slow-speed acid can slowly release hydrogen chloride at 30-70 ° C, and the pH of the system is adjusted by releasing hydrogen chloride to realize the viscosity of the system. Increase
  • the reinforcing agent is sodium silicate
  • the modulus is 3.0-3.5
  • the mass fraction in the total mass of the system is 1.0%-3.0%
  • the stability of the auto-acid-induced viscosity-increasing regulation system can be enhanced by adding the reinforcing agent
  • the liquid distribution water is fresh water or treated oil field reinjected sewage.
  • the medium and low temperature reservoir temperature is 30 ° C to 70 ° C.
  • anionic polymer in the liquid water, stir for 30 minutes to dissolve; then add sodium alkyl sulfate surfactant, methyl propylene diamine, slow-speed acid, enhancer, Stirring for 5 minutes until it is fully dispersed and dissolved, thereby obtaining a self-generated acid-induced viscosity-enhancing regulation system with oil washing effect; the mass fraction of anionic polymer in the autogenous acid-induced viscosity-increasing control system with oil washing effect is 0.1% ⁇ 0.2%, the mass fraction of sodium alkyl sulfate surfactant is 0.5% to 1.5%, the mass fraction of methyl propylene diamine is 0.3% to 0.8%, and the mass fraction of slow acid is 1.0% to 3.5%.
  • the mass fraction of the agent is from 1.0% to 3.0%, and the balance is the liquid water to be described.
  • a self-generated acid-induced viscosity-increasing control system with oil washing effect can reduce the oil-water interfacial tension to 10 -2 mN/m, the viscosity at 30 °C for 15 days is 3.3 ⁇ 10 4 mPa ⁇ s, and the aging at 50 °C for 10 days.
  • the viscosity was 2.1 ⁇ 10 4 mPa ⁇ s, and the viscosity at 70 ° C for 8 days was 1.5 ⁇ 10 4 mPa ⁇ s.
  • the present invention has the following beneficial effects:
  • a self-generated acid-induced viscosity-increasing control system with oil washing effect uses anionic polymer, sodium alkyl sulfate surfactant, methyl propylene diamine, slow-speed acid, and enhancer. Synergistic effect.
  • the addition of sodium alkyl sulfate surfactant can make the autotrophic acid-induced viscosity-promoting system have higher interfacial activity in the initial stage, and significantly reduce the oil-water interfacial tension.
  • the addition of slow-acting acid can slowly release hydrogen chloride to control the autotrophic acid-induced viscosity-regulating system.
  • the viscosity increases time
  • the addition of anionic polymer can increase the viscoelasticity of the serotonin-induced viscosity-regulating system
  • the addition of the enhancer can improve the thermal stability of the autotrophic acid-induced viscosity-enhancing system.
  • a self-generated acid-induced viscosity-enhancing control system with washing oil has a high interfacial activity in the initial stage, which can reduce the oil-water interfacial tension to the order of 10 -2 mN/m, and significantly improve the washing of the oil-displacing agent.
  • the oil efficiency and the viscosity after aging can reach 1.0 ⁇ 10 4 mPa ⁇ s or more, which can realize the dual role of deep regulation of the formation to increase the volume of the oil displacement agent.
  • the viscosity of a self-generated acid-induced viscosity-increasing control system with oil washing effect increases slowly with the increase of aging time.
  • the viscosity of aging for 8 days at 70 °C increases from the initial 7.6 mPa ⁇ s to 1.5 ⁇ 10 4 .
  • mPa ⁇ s can meet the medium and low temperature reservoir conditions of 30-70 °C, which overcomes the difficulty of increasing the viscosity of the conventional control system or the environmental protection type, and can not be deeply injected.
  • a self-generated acid-induced viscosity-enhancing control system with oil washing effect has good compatibility with each other, and has the characteristics of simple preparation and easy on-site construction.
  • a self-generated acid-induced viscosity-increasing control system with oil washing effect has low initial viscosity, good injectability and easy access to the deep part of the formation.
  • Fig. 1 is a rheological curve of a self-generated acid-induced viscosity-increasing control system of Example 1 before and after aging at 70 °C.
  • Fig. 2 is a rheological curve of a self-generated acid-induced viscosity-increasing control system of Example 2 before and after aging at 50 °C.
  • Fig. 3 is a rheological curve of a self-generated acid-induced viscosity-increasing control system of Example 3 before and after aging at 30 °C.
  • a self-generated acid-induced viscosity-increasing control system with oil washing effect including: anionic polymer, mass fraction of 0.15%; sodium alkyl sulfate surfactant, mass fraction of 1.5%; methyl propylene diamine, mass fraction 0.8%; slow acid, mass fraction of 1.0%; enhancer, mass fraction of 1.0%; balance of liquid water, mass fraction of 96.55%, the sum of the mass fraction of each component is 100%.
  • a self-generated acid-induced viscosity-increasing control system with oil washing effect comprising: anionic polymer, mass fraction of 0.1%; sodium alkyl sulfate surfactant, mass fraction of 1.0%; methyl propylene diamine, mass fraction 0.6%; slow acid, mass fraction of 2.0%; enhancer, mass fraction of 2.0%; balance of liquid water, mass fraction of 94.3%, the sum of the mass fraction of each component is 100%.
  • a self-generated acid-induced viscosity-increasing control system with oil washing effect comprising: anionic polymer, mass fraction of 0.2%; sodium alkyl sulfate surfactant, mass fraction of 0.5%; methyl propylene diamine, mass fraction It is 0.3%; slow acid, the mass fraction is 3.5%; the reinforcing agent, the mass fraction is 3.0%; the balance is liquid, the mass fraction is 92.5%, and the sum of the mass fractions of each component is 100%.

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Abstract

本发明属于油田化学领域,具体地,涉及一种用于中低温油藏的一种兼具洗油作用的自生酸诱导增粘调控体系法,其包括:阴离子聚合物、烷基硫酸钠表面活性剂、甲基丙二胺、缓速酸、增强剂和配液水,质量组份如下:阴离子聚合物0.1%~0.2%;烷基硫酸钠表面活性剂0.5%~1.5%;甲基丙二胺0.3%~0.8%;缓速酸1.0%~3.5%;增强剂1.0%~3.0%;余量为配液水,各组分质量分数之和为100%。本发明具有以下有益效果:显著提高驱油剂的洗油效率,粘度增加后可实现储层深部调控提高驱油剂波及体积的双重作用,克服了常规调控体系功能单一、粘度增加快或环保型差,无法深部注入的难点。

Description

一种兼具洗油作用的自生酸诱导增粘调控体系及制备方法 技术领域
本发明属于油田化学领域,具体地,涉及一种用于中低温油藏的兼具洗油作用的自生酸诱导增粘调控体系及制备方法。
技术背景
我国是世界上注水开发油田比例较高的国家之一,水驱开发储量占总储量的70%以上。但油田的长期注水开发,导致地层的非均质性加剧,水驱波及不均进一步演变成大孔道窜流,导致注入水沿高渗层向油井突进,油井产出水过多,逐步进入高含水期,势必造成采收率过低。但高含水期开发阶段的油田仍有大量的剩余油未被挖潜,只是由于储层的分异严重,导致储层的动用程度受到限制。因此,高含水期开发阶段的油田仍具备挖潜的潜力。目前提高高含水期开发阶段油田剩余油高效挖潜的措施主要从两个方面开展工作:一个途径是通过向地层中注入调控剂,提高驱油剂的波及系数;另外一个途径是向地层中注入可以改变岩石表面的润湿性和减小毛细管阻力效应的驱油剂,提高驱油剂的洗油效率。CN103980872公开了一种适用于低温油藏的环境友好型冻胶堵剂,该调控剂由两亲聚合物和有机锆组成,能够适用于25~35℃的油藏地层深部调控。该调控剂具有环境友好型的特点,但成胶温度窄,尤其不适于夏季矿场的施工。CN86108877公开了一种锆冻胶堵水调控剂,由聚丙烯酰胺(PAM)或甲叉基聚丙烯酰胺(MPAM)与交联剂无机锆化合物组成。无机锆化合物有氧氯化锆、四氯化锆、硫酸锆、硝酸锆等。该锆冻胶调控剂可满足温度低于70℃油藏堵水,由于锆冻胶体系成胶时间快,现场施工过程中只能采取聚丙烯酰胺(PAM)或甲叉基聚丙烯酰胺(MPAM)溶液与交联剂无机锆化合物交替顺序注入,增加了矿场施工工序,且形成的锆冻胶调控体系成胶迅速,施工过程中存在一定的工程风险。目前研发的储层调控剂主要通过提高驱油剂的波及系数实现原油采收率的提高,较少兼顾储层调控剂本身的洗油效率。CN103254883A公开了一种用于提高高温高盐高硬度油藏原油采收率的驱油剂,由氧化胺型两性表面活性剂和烷基酚聚氧乙烯醚羧酸表面活性剂组成,能够降低油水界面张力达10 -2mN/m。但该 驱油体系适用于相对均质的地层,对于存在渗流优势通道的高含水非均质油藏,注入的驱油剂单独使用时流度不能很好的控制,容易沿高渗层指进,降低了驱油效果。
鉴于中低温油藏常规调控剂无法兼顾洗油效率、单一表面活性剂高含水油藏适应差的难题,需要研发一种新的储层调控体系既能够提高驱油剂的波及体积,同时又能够提高驱油剂的洗油效率,达到长期有效的水驱效果。
发明内容
针对现有技术的不足,本发明提供一种用于中低温油藏的兼具洗油作用的自生酸诱导增粘调控体系及制备方法。该体系初始阶段具有降低油水界面张力提高洗油效率的能力,粘度增加后可实现地层深部调控扩大波及体积的双重作用。
为实现上述目的,本发明采用下述方案:
一种兼具洗油作用的自生酸诱导增粘调控体系,包括:阴离子聚合物、烷基硫酸钠表面活性剂、甲基丙二胺、缓速酸、增强剂和配液水,质量组份如下:
Figure PCTCN2017119361-appb-000001
余量为配液水,各组分质量分数之和为100%。
优选的,阴离子聚合物分子量为1000万~1200万,水解度为20~25%,通过加入聚合物可提高注入初期驱替介质粘度和携带缓速酸的作用;
优选的,所述的烷基硫酸钠,具有结构式:
Figure PCTCN2017119361-appb-000002
式中,m为烷基基团的加和数10~14,优选为11;M为金属离子,优选为钠;
优选的,所述的甲基丙二胺,具有结构式:
Figure PCTCN2017119361-appb-000003
式中,n为1~3,优选为2。
优选的,缓速酸为聚氯乙烯粉,粒径在1~5μm之间分布,该缓速酸在30~70℃条件下可以缓慢释放氯化氢,通过释放的氯化氢调整体系的pH值实现体系粘度的增加;
优选的,增强剂为硅酸钠,模数为3.0~3.5,在体系总质量中的质量分数为1.0%~3.0%,通过加入增强剂可以强化形成自生酸诱导增粘调控体系的稳定性;
所述的配液水为清水或经过处理的油田回注污水。
所述的中低温油藏温度为30℃~70℃。
上述的一种兼具洗油作用的自生酸诱导增粘调控体系的制备方法,其特征在于:包括如下步骤:
室温下(20±5℃),在配液水中先加入阴离子聚合物,搅拌30分钟待其溶解后;依次加入烷基硫酸钠表面活性剂、甲基丙二胺、缓速酸、增强剂,搅拌5分钟待其充分分散溶解,从而得到一种兼具洗油作用的自生酸诱导增粘调控体系;兼具洗油作用的自生酸诱导增粘调控体系中阴离子聚合物的质量分数为0.1%~0.2%,烷基硫酸钠表面活性剂的质量分数为0.5%~1.5%,甲基丙二胺的质量分数为0.3%~0.8%,缓速酸的质量分数为1.0%~3.5%,增强剂的质量分数为1.0%~3.0%,余量为所述的配液水。
一种兼具洗油作用的自生酸诱导增粘调控体系可降低油水界面张力达10 -2mN/m,30℃老化15天的粘度为3.3×10 4mPa·s,50℃老化10天的粘度为2.1×10 4mPa·s,70℃老化8天的粘度为1.5×10 4mPa·s。
相对于现有技术,本发明具有以下有益效果:
1、一种兼具洗油作用的自生酸诱导增粘调控体系采用阴离子聚合物、烷基硫酸钠表面活性剂、甲基丙二胺、缓速酸、增强剂,各成份之间具有较好的协同效应。烷基硫酸钠表面活性剂的加入可使自生酸诱导增粘调控体系初始阶段具有较高的界面活性,显著降低油水界面张力,缓速酸的加入可缓慢释放氯化氢控制自生酸诱导增粘调控体系的粘度增加时间,阴离子聚合物的加入可提高自生酸诱导增粘调控体 系的粘弹性,增强剂的加入可以提高自生酸诱导增粘调控体系的热稳定性。
2、采用的一种兼具洗油作用的自生酸诱导增粘调控体系初始阶段具有较高的界面活性,可使油水界面张力降低到10 -2mN/m数量级,显著提高驱油剂的洗油效率,老化后粘度可达1.0×10 4mPa·s以上,可实现地层深部调控提高驱油剂波及体积的双重作用。
3、采用的一种兼具洗油作用的自生酸诱导增粘调控体系粘度随老化时间的增加而缓慢增加,70℃条件下老化8天粘度由初始的7.6mPa·s增加至1.5×10 4mPa·s,可满足30~70℃的中低温油藏条件使用,克服了常规调控体系粘度增加快或环保型差,无法深部注入的难点。
4、采用的一种兼具洗油作用的自生酸诱导增粘调控体系各成份之间具有较好的配伍性,具有配制简单,易于现场施工的特点。
5、采用的一种兼具洗油作用的自生酸诱导增粘调控体系初始粘度低,注入性好,易于进入地层深部。
附图说明:
图1是实施例1的一种兼具洗油作用的自生酸诱导增粘调控体系在70℃老化前后的流变曲线。
图2是实施例2的一种兼具洗油作用的自生酸诱导增粘调控体系在50℃老化前后的的流变曲线。
图3是实施例3的一种兼具洗油作用的自生酸诱导增粘调控体系在30℃老化前后的流变曲线。
具体实施方式
下面通过实施例对本发明做进一步说明,但不限于此。
实施例1:
一种兼具洗油作用的自生酸诱导增粘调控体系,包括:阴离子聚合物,质量分数为0.15%;烷基硫酸钠表面活性剂,质量分数为1.5%;甲基丙二胺,质量分数为 0.8%;缓速酸,质量分数为1.0%;增强剂,质量分数为1.0%;余量配液清水,质量分数为96.55%,各组分质量分数之和为100%。
室温下(20±5℃),在96.55g配液水中先加入0.15g阴离子聚合物,搅拌30分钟待其溶解后;依次加入1.5g烷基硫酸钠表面活性剂、0.8g甲基丙二胺、1g缓速酸、1g增强剂,搅拌5分钟待其充分溶解分散,从而得到一种兼具洗油作用的自生酸诱导增粘调控体系;该体系70℃条件下可降低油水界面张力5.86×10 -2mN/m,70℃条件下初始粘度为7.6mPa·s,老化8天后的粘度为1.5×10 4mPa·s。
实施例2:
一种兼具洗油作用的自生酸诱导增粘调控体系,包括:阴离子聚合物,质量分数为0.1%;烷基硫酸钠表面活性剂,质量分数为1.0%;甲基丙二胺,质量分数为0.6%;缓速酸,质量分数为2.0%;增强剂,质量分数为2.0%;余量配液清水,质量分数为94.3%,各组分质量分数之和为100%。
室温下(20±5℃),在94.3g配液水中先加入0.1g阴离子聚合物,搅拌30分钟待其溶解后;依次加入1.0g烷基硫酸钠表面活性剂、0.6g甲基丙二胺、2g缓速酸、2g增强剂,搅拌5分钟待其充分溶解分散,从而得到一种兼具洗油作用的自生酸诱导增粘调控体系;该体系50℃条件下可降低油水界面张力4.25×10 -2mN/m,50℃条件下初始粘度为15.3mPa·s,老化10天后的粘度为2.1×10 4mPa·s。
实施例3:
一种兼具洗油作用的自生酸诱导增粘调控体系,包括:阴离子聚合物,质量分数为0.2%;烷基硫酸钠表面活性剂,质量分数为0.5%;甲基丙二胺,质量分数为0.3%;缓速酸,质量分数为3.5%;增强剂,质量分数为3.0%;余量配液清水,质量分数为92.5%,各组分质量分数之和为100%。
室温下(20±5℃),在92.5g配液水中先加入0.2g阴离子聚合物,搅拌30分钟待其溶解后;依次加入0.5g烷基硫酸钠表面活性剂、0.3g表面活性剂、3.5g缓速酸、3.0g增强剂,搅拌5分钟待其充分溶解分散,从而得到一种兼具洗油作用的自生酸 诱导增粘调控体系;该液体系30℃条件下可降低油水界面张力2.73×10 -2mN/m,30℃条件下初始粘度为33.7mPa·s,老化15天后的粘度为3.3×10 4mPa·s。

Claims (10)

  1. 一种用于中低温油藏的兼具洗油作用的自生酸诱导增粘调控体系,包括:阴离子聚合物、烷基硫酸钠表面活性剂、甲基丙二胺、缓速酸、增强剂和配液水,其特征在于,质量组份如下:
    Figure PCTCN2017119361-appb-100001
  2. 根据权利要求1所述的一种兼具洗油作用的自生酸诱导增粘调控体系,其特征在于,阴离子聚合物分子量为1000万~1200万,水解度为20~25%。
  3. 根据权利要求1-2所述的一种兼具洗油作用的自生酸诱导增粘调控体系,其特征在于,所述的烷基硫酸钠,具有结构式:
    Figure PCTCN2017119361-appb-100002
    式中,m为烷基基团的加和数10~14,M为金属离子。
  4. 根据权利要求1-3所述的一种兼具洗油作用的自生酸诱导增粘调控体系,其特征在于,所述的甲基丙二胺,具有结构式:
    Figure PCTCN2017119361-appb-100003
    式中,n为1~3。
  5. 根据权利要求1-4所述的一种兼具洗油作用的自生酸诱导增粘调控体系,其特征在于,缓速酸为聚氯乙烯粉,粒径在1~5μm之间分布。
  6. 根据权利要求1-5所述的一种兼具洗油作用的自生酸诱导增粘调控体系,其特征在于,增强剂为硅酸钠,模数为3.0~3.5,在体系总质量中的质量分数为1.0%~3.0%。
  7. 根据权利要求1-6所述的一种兼具洗油作用的自生酸诱导增粘调控体系,其特征在于,所述的配液水为清水或经过处理的油田回注污水。
  8. 根据权利要求1-7所述的一种兼具洗油作用的自生酸诱导增粘调控体系,其特征在于,所述的中低温油藏温度为30℃~70℃。
  9. 根据权利要求1-8所述的一种兼具洗油作用的自生酸诱导增粘调控体系,其特征在于,m为11,n为2,M为钠。
  10. 权利要求1-9所述的一种兼具洗油作用的自生酸诱导增粘调控体系的制备方法,其特征在于:包括如下步骤:室温下(20±5℃),在配液水中先加入阴离子聚合物,搅拌30分钟待其溶解后;依次加入烷基硫酸钠表面活性剂、甲基丙二胺、缓速酸、增强剂,搅拌5分钟待其充分分散溶解,从而得到一种兼具洗油作用的自生酸诱导增粘调控体系;兼具洗油作用的自生酸诱导增粘调控体系中阴离子聚合物的质量分数为0.1%~0.2%,烷基硫酸钠表面活性剂的质量分数为0.5%~1.5%,甲基丙二胺的质量分数为0.3%~0.8%,缓速酸的质量分数为1.0%~3.5%,增强剂的质量分数为1.0%~3.0%,余量为所述的配液水。
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114645690A (zh) * 2020-12-21 2022-06-21 中国石油化工股份有限公司 一种冻胶分散体复合调驱工艺
CN115612469A (zh) * 2021-07-15 2023-01-17 大庆油田有限责任公司 一种温度和矿化度响应型低初始粘度弱凝胶体系及其制备方法

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106634927A (zh) * 2016-12-15 2017-05-10 中国石油大学(华东) 一种兼具洗油作用的自生酸诱导增粘调控体系及制备方法
CN108384529B (zh) * 2018-05-08 2020-09-15 中联煤层气有限责任公司 一种油包水乳状液流体、制备方法及石油开采方法
CN114716995A (zh) * 2021-01-05 2022-07-08 中国石油化工股份有限公司 一种自生酸及其制备方法和应用

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103450872A (zh) * 2012-05-28 2013-12-18 中国石油天然气股份有限公司 一种自生酸体系及其应用
CN103805159A (zh) * 2014-02-18 2014-05-21 中联煤层气有限责任公司 酸基粘弹性流体、其制备方法及油气储层或煤层的处理方法
CN103952134A (zh) * 2014-05-16 2014-07-30 中联煤层气有限责任公司 一种粘弹性酸化液及其制备方法
CN106634927A (zh) * 2016-12-15 2017-05-10 中国石油大学(华东) 一种兼具洗油作用的自生酸诱导增粘调控体系及制备方法

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1079486C (zh) * 1999-04-30 2002-02-20 大庆石油管理局 驱油组合物及驱油注液
CN1148432C (zh) * 2002-10-28 2004-05-05 四川大学 高增粘疏水缔合聚合物驱油剂的制备方法
CN102453167B (zh) * 2010-10-25 2013-09-04 中国石油化工股份有限公司 聚合物驱油剂及其制备方法和油藏驱油方法

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103450872A (zh) * 2012-05-28 2013-12-18 中国石油天然气股份有限公司 一种自生酸体系及其应用
CN103805159A (zh) * 2014-02-18 2014-05-21 中联煤层气有限责任公司 酸基粘弹性流体、其制备方法及油气储层或煤层的处理方法
CN103952134A (zh) * 2014-05-16 2014-07-30 中联煤层气有限责任公司 一种粘弹性酸化液及其制备方法
CN106634927A (zh) * 2016-12-15 2017-05-10 中国石油大学(华东) 一种兼具洗油作用的自生酸诱导增粘调控体系及制备方法

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114645690A (zh) * 2020-12-21 2022-06-21 中国石油化工股份有限公司 一种冻胶分散体复合调驱工艺
CN114645690B (zh) * 2020-12-21 2024-03-26 中国石油化工股份有限公司 一种冻胶分散体复合调驱工艺
CN115612469A (zh) * 2021-07-15 2023-01-17 大庆油田有限责任公司 一种温度和矿化度响应型低初始粘度弱凝胶体系及其制备方法
CN115612469B (zh) * 2021-07-15 2024-02-02 大庆油田有限责任公司 一种温度和矿化度响应型低初始粘度弱凝胶体系及其制备方法

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