CN115011319B - A three-phase foam system for temperature-resistant and salt-resistant oil displacement, its preparation method and application - Google Patents
A three-phase foam system for temperature-resistant and salt-resistant oil displacement, its preparation method and application Download PDFInfo
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- 239000006260 foam Substances 0.000 title claims abstract description 62
- 238000006073 displacement reaction Methods 0.000 title claims abstract description 18
- 150000003839 salts Chemical class 0.000 title claims abstract description 17
- 238000002360 preparation method Methods 0.000 title claims abstract description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 31
- 238000005187 foaming Methods 0.000 claims abstract description 20
- 239000007788 liquid Substances 0.000 claims abstract description 14
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims abstract description 10
- JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000011575 calcium Substances 0.000 claims abstract description 10
- 229910001424 calcium ion Inorganic materials 0.000 claims abstract description 10
- 229910001425 magnesium ion Inorganic materials 0.000 claims abstract description 10
- 238000000034 method Methods 0.000 claims abstract description 10
- 238000011161 development Methods 0.000 claims abstract description 7
- 238000003756 stirring Methods 0.000 claims description 30
- 239000010881 fly ash Substances 0.000 claims description 18
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 14
- 239000011734 sodium Substances 0.000 claims description 14
- 229910052708 sodium Inorganic materials 0.000 claims description 14
- 239000002689 soil Substances 0.000 claims description 11
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 6
- 239000008367 deionised water Substances 0.000 claims description 6
- 229910021641 deionized water Inorganic materials 0.000 claims description 6
- 230000018109 developmental process Effects 0.000 claims description 6
- 239000004033 plastic Substances 0.000 claims description 6
- 230000032683 aging Effects 0.000 claims description 5
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 3
- 239000001569 carbon dioxide Substances 0.000 claims description 3
- 230000002431 foraging effect Effects 0.000 claims description 3
- 239000008398 formation water Substances 0.000 claims description 3
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 229910001415 sodium ion Inorganic materials 0.000 claims description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 2
- 238000012546 transfer Methods 0.000 claims description 2
- 239000004711 α-olefin Substances 0.000 claims description 2
- PSBDWGZCVUAZQS-UHFFFAOYSA-N (dimethylsulfonio)acetate Chemical compound C[S+](C)CC([O-])=O PSBDWGZCVUAZQS-UHFFFAOYSA-N 0.000 claims 1
- 229940117986 sulfobetaine Drugs 0.000 claims 1
- 238000011084 recovery Methods 0.000 abstract description 14
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 abstract description 12
- 239000011780 sodium chloride Substances 0.000 abstract description 6
- 230000005465 channeling Effects 0.000 abstract description 2
- 239000003921 oil Substances 0.000 abstract 3
- 239000010779 crude oil Substances 0.000 abstract 1
- 239000007789 gas Substances 0.000 description 21
- 239000002245 particle Substances 0.000 description 16
- 239000012071 phase Substances 0.000 description 14
- 239000000243 solution Substances 0.000 description 11
- 239000003945 anionic surfactant Substances 0.000 description 10
- 239000002270 dispersing agent Substances 0.000 description 9
- 239000007790 solid phase Substances 0.000 description 9
- 239000002888 zwitterionic surfactant Substances 0.000 description 8
- 239000012530 fluid Substances 0.000 description 6
- 230000001965 increasing effect Effects 0.000 description 6
- 101150101199 CHSB gene Proteins 0.000 description 5
- 238000007789 sealing Methods 0.000 description 5
- 239000000725 suspension Substances 0.000 description 5
- 238000010586 diagram Methods 0.000 description 4
- 238000002347 injection Methods 0.000 description 4
- 239000007924 injection Substances 0.000 description 4
- 229910017053 inorganic salt Inorganic materials 0.000 description 4
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 230000035699 permeability Effects 0.000 description 3
- 239000012266 salt solution Substances 0.000 description 3
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 3
- 230000007423 decrease Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- IXOCGRPBILEGOX-UHFFFAOYSA-N 3-[3-(dodecanoylamino)propyl-dimethylazaniumyl]-2-hydroxypropane-1-sulfonate Chemical group CCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC(O)CS([O-])(=O)=O IXOCGRPBILEGOX-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
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- 239000002994 raw material Substances 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/58—Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/58—Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids
- C09K8/584—Compositions 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
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/58—Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids
- C09K8/594—Compositions used in combination with injected gas, e.g. CO2 orcarbonated gas
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- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Life Sciences & Earth Sciences (AREA)
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- Engineering & Computer Science (AREA)
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Abstract
Description
技术领域technical field
本发明涉及油田勘探技术领域,具体涉及一种耐温耐盐驱油用三相泡体系及其制备方法与应用。The invention relates to the technical field of oil field exploration, in particular to a temperature-resistant and salt-resistant three-phase foam system for oil flooding, a preparation method and application thereof.
背景技术Background technique
随着我国越来越多的油田进入开发中后期,注水开发的采收率逐渐降低,采出液含水量逐渐增大。泡沫注入是一种效果显著的防窜方法,其防窜机理主要是通过泡沫对高渗带的选择性封堵实现液流转向作用,同时泡沫具有很高表观粘度可以有效控制气油流度比,从而最大程度提高气体波及体积。但是泡沫本身面临储层条件下稳定性差的问题,因此目前的研究大都着眼于提高泡沫在恶劣条件下的稳定性。As more and more oilfields in my country enter the middle and late stage of development, the recovery rate of water flooding development gradually decreases, and the water content of produced fluid increases gradually. Foam injection is an effective anti-channeling method. The anti-channeling mechanism is mainly through the selective plugging of the high permeability zone by the foam to realize the diversion of the liquid flow. At the same time, the foam has a high apparent viscosity and can effectively control the gas-oil mobility. ratio, thereby maximizing the gas sweep volume. But the foam itself faces the problem of poor stability under reservoir conditions, so most of the current research focuses on improving the stability of foam under harsh conditions.
针对这一问题,国内外的研究人员进行了大量的研究,纳米颗粒稳定泡沫、有机胺稳定泡沫、聚合物稳定泡沫、羧甲基纤维素稳定泡沫等多种泡沫体系被证明可用于提高采收率作业。但因为价格、不耐高温、不耐盐等局限性,现有体系很难在油田现场起到作用。In response to this problem, researchers at home and abroad have conducted a lot of research, and various foam systems such as nanoparticle-stabilized foam, organic amine-stabilized foam, polymer-stabilized foam, and carboxymethylcellulose-stabilized foam have been proven to be used to improve oil recovery. rate work. However, due to limitations such as price, intolerance to high temperature, and intolerance to salt, it is difficult for the existing system to play a role in the oil field.
鉴于此,本发明提供一种耐温耐盐驱油用三相泡沫体系及其制备方法,原料廉价易得,在复杂油藏条件下具有良好的效果。In view of this, the present invention provides a temperature-resistant and salt-resistant three-phase foam system for oil flooding and a preparation method thereof. The raw materials are cheap and easy to obtain, and have good effects under complex reservoir conditions.
发明内容Contents of the invention
本发明的目的在于,针对现有技术的上述不足,提供了一种耐温耐盐驱油用三相泡体系及其制备方法与应用。The object of the present invention is to provide a temperature-resistant and salt-resistant three-phase foam system for oil flooding, its preparation method and application, aiming at the above-mentioned shortcomings of the prior art.
为实现上述目的,本发明采用如下的技术方案:To achieve the above object, the present invention adopts the following technical solutions:
本发明的第一目的在于提供一种耐温耐盐驱油用三相泡沫体系,由阴离子表面活性剂、两性离子表面活性剂、固相颗粒、分散剂、气体和水制成,按重量份数计所述阴离子表面活性剂的质量份数为0.3-0.7份、两性离子表面活性剂0.3-0.5份、固相颗粒3-7份、分散剂2-5份、水100份、所述气体与所述驱油用三相泡沫体系的体积比为1:1-4:1。The first object of the present invention is to provide a three-phase foam system for temperature-resistant and salt-resistant oil displacement, which is made of anionic surfactant, zwitterionic surfactant, solid phase particles, dispersant, gas and water, in parts by weight The mass fraction of the anionic surfactant is 0.3-0.7 parts, 0.3-0.5 parts of zwitterionic surfactant, 3-7 parts of solid phase particles, 2-5 parts of dispersant, 100 parts of water, the gas The volume ratio to the three-phase foam system for oil displacement is 1:1-4:1.
进一步的,所述的阴离子表面活性剂为α—烯烃磺酸钠(AOS)和十二烷基苯磺酸钠(SDBS)中的一种或两种。Further, the anionic surfactant is one or both of sodium α-olefin sulfonate (AOS) and sodium dodecylbenzenesulfonate (SDBS).
进一步的,所述的两性离子表面活性剂为椰油酰胺丙基羟磺基甜菜碱(CHSB)。Further, the zwitterionic surfactant is cocamidopropyl hydroxysultaine (CHSB).
进一步的,所述的固相颗粒为粉煤灰。Further, the solid phase particles are fly ash.
进一步的,所述分散剂为钠土。Further, the dispersant is sodium earth.
进一步的,所述气体为二氧化碳。Further, the gas is carbon dioxide.
本发明的第二目的在于提供上述耐温耐盐驱油用三相泡沫体系的制备方法,包括以下步骤:The second object of the present invention is to provide a method for preparing the above-mentioned three-phase foam system for temperature-resistant and salt-resistant oil flooding, comprising the following steps:
步骤S1,将一定量的去离子水倒入烧杯中,向烧杯中加入无机盐,配制模拟地层水;Step S1, pouring a certain amount of deionized water into a beaker, adding inorganic salts into the beaker to prepare simulated formation water;
步骤S2,将烧杯置于磁力搅拌器上,设定第一预设转速,向步骤S1的烧杯中加入一定量的阴离子表面活性剂,搅拌至完全溶解;Step S2, placing the beaker on a magnetic stirrer, setting the first preset speed, adding a certain amount of anionic surfactant to the beaker in step S1, and stirring until completely dissolved;
步骤S3,向步骤S2的中加入一定量的两性离子表面活性剂,搅拌至完全溶解;Step S3, adding a certain amount of zwitterionic surfactant to step S2, stirring until completely dissolved;
步骤S4,向步骤S3的中加入一定量的分散剂,搅拌使其充分悬浮;Step S4, adding a certain amount of dispersant to step S3, stirring to make it fully suspended;
步骤S5,向步骤S4的中加入一定量的固相颗粒,搅拌使其充分悬浮,得发泡液;Step S5, adding a certain amount of solid phase particles to the step S4, stirring to make it fully suspended, to obtain a foaming liquid;
步骤S6,将搅拌好的发泡液用保鲜膜封口,放在恒温箱中老化;Step S6, sealing the stirred foaming solution with a plastic wrap, and placing it in an incubator for aging;
步骤S7,将老化后的发泡液转移至高速搅拌器中,设定第二预设转速,向其中通入二氧化碳10min,设定转速8000r/min,搅拌时间2min,即得驱油用三相泡沫体系。Step S7, transfer the aged foaming liquid to a high-speed agitator, set the second preset speed, pass carbon dioxide into it for 10 minutes, set the speed at 8000r/min, and stir for 2 minutes to obtain the three-phase oil displacement foam system.
进一步的,所述第一预设转速为350r/min~400r/min,所述第二预设转速为6000r/min~8000r/min。Further, the first preset rotation speed is 350r/min-400r/min, and the second preset rotation speed is 6000r/min-8000r/min.
进一步的,步骤S6中老化的时间为48h~60h。Further, the aging time in step S6 is 48h-60h.
本发明的第三目的提供上述驱油用三相泡沫体系溶液用于制备油田泡沫调驱剂。The third object of the present invention is to provide the above-mentioned three-phase foam system solution for oil displacement to be used for preparing oilfield foam control and displacement agent.
与现有技术比较,本发明提供的技术方案带来的有益效果是:Compared with the prior art, the beneficial effects brought by the technical solution provided by the present invention are:
(1)本发明的驱油用三相泡沫体系在80℃、100000mg/L NaCl、钙镁离子浓度500mg/L的条件下,100ml发泡液通过Blender-Waring法产生的泡沫体积350mL,半衰期为34min,在水驱、CO2气驱后,注入0.5PV泡沫再进行CO2气驱,最终原油采收率较水驱提高39.15%,为70.78%。而且本发明在高温情况下,仍然能够保持长时间泡沫稳定,同时对钙镁离子的耐受性好,有效减少气窜,启动水驱、气驱后的残余油,钠离子浓度低于150000mg/L、钙镁离子浓度低于5000mg/L、温度低于120℃时均能保持泡沫稳定,显著提高采收率,适用于高温高盐常规砂岩油藏的二次开发。(1) Under the conditions of 80°C, 100000mg/L NaCl, and 500mg/L of calcium and magnesium ion concentration in the three-phase foam system for oil displacement of the present invention, the volume of foam produced by 100ml of foaming liquid by the Blender-Waring method is 350mL, and the half-life is At 34 minutes, after water flooding and CO 2 gas flooding, 0.5PV foam was injected and CO 2 gas flooding was carried out. The final oil recovery rate was 70.78%, which was 39.15% higher than that of water flooding. Moreover, the present invention can still maintain long-term foam stability under high temperature conditions, and at the same time, has good tolerance to calcium and magnesium ions, effectively reduces gas channeling, and the residual oil after water flooding and gas flooding is started, and the sodium ion concentration is lower than 150,000mg/ L. When the concentration of calcium and magnesium ions is lower than 5000mg/L and the temperature is lower than 120°C, the foam can be kept stable, and the recovery rate can be significantly improved. It is suitable for the secondary development of high-temperature and high-salt conventional sandstone reservoirs.
(2)本发明提供的驱油用三相泡沫体系通过引入固相颗粒粉煤灰,形成气-液-固三相泡沫体系,能够对高含水、高渗透区域进行封堵,使驱替液转入此前未波及的低渗透、高含油区域,可用于常规砂岩油藏水驱、气驱后的二次开发。驱油用三相泡沫体系中的阴离子表面活性剂与带正电的粉煤灰颗粒能够发生协同增效作用。部分阴离子表面活性剂吸附在粉煤灰颗粒的表面,使粉煤灰颗粒的疏水性增强,在气液界面上排列而不是进入液相从而增强泡沫的稳定性。粉煤灰的悬浮性差,在溶液中分散后易发生沉降,因此需在体系中加入钠土作为分散剂。钠土呈负电性,粉煤灰呈正电性,二者易发生吸引作用,钠土附着在粉煤灰颗粒上,使颗粒的密度减小,悬浮性增强,能够更长时间保持稳定,提高三相泡沫的性能。(2) The three-phase foam system for oil displacement provided by the present invention forms a gas-liquid-solid three-phase foam system by introducing solid-phase particle fly ash, which can block high water content and high permeability areas, and make the displacement fluid It can be used for secondary development after water flooding and gas flooding of conventional sandstone reservoirs, which have been transferred to low-permeability and high-oil-bearing areas that have not been affected before. Anionic surfactants and positively charged fly ash particles in three-phase foam systems for oil displacement can have a synergistic effect. Part of the anionic surfactant is adsorbed on the surface of fly ash particles, which enhances the hydrophobicity of fly ash particles, arranges on the gas-liquid interface instead of entering the liquid phase, thereby enhancing the stability of the foam. Fly ash has poor suspensibility and is prone to sedimentation after being dispersed in the solution, so it is necessary to add sodium soil into the system as a dispersant. Sodium soil is negatively charged, and fly ash is positively charged, and the two are prone to attract. The sodium soil is attached to the fly ash particles, which reduces the density of the particles and enhances the suspension, which can maintain stability for a longer time and improve the three Phase foam properties.
(3)本发明提供的制备方法的技术条件温和,简单易行,具有环境友好性和广阔的市场开发潜力。(3) The preparation method provided by the invention has mild technical conditions, is simple and easy to implement, has environmental friendliness and broad market development potential.
附图说明Description of drawings
图1为粉煤灰提高泡沫稳定性原理示意图;Fig. 1 is the principle schematic diagram that fly ash improves foam stability;
图2为钠土对粉煤灰悬浮性的影响图;显然加入钠土后的粉煤灰悬浮液沉降时间延后3h,粉煤灰颗粒尺寸为微米级,悬浮性差,选用钠土作为悬浮剂,在粉煤灰颗粒上附着,可有效延缓悬浮液沉降时间。Figure 2 is a diagram showing the influence of sodium soil on the suspension of fly ash; it is obvious that after adding sodium soil, the settling time of fly ash suspension is delayed by 3 hours, and the particle size of fly ash is micron, and the suspension is poor, so sodium soil is selected as the suspending agent , attached to the fly ash particles, which can effectively delay the settling time of the suspension.
图3为岩心驱替实验数据;泡沫驱阶段,含水率下降,注入压力升高,采收率提高,说明该发明能够起到调整注入剖面、提高注入压力、提高采收率的作用;在80℃、NaCl浓度100000mg/L、钙镁离子浓度500mg/L的条件下,原油采收率较水驱提高39.15%;Fig. 3 is the data of the core displacement experiment; in the stage of foam flooding, the water cut decreases, the injection pressure increases, and the recovery factor increases, indicating that the invention can play the role of adjusting the injection profile, increasing the injection pressure, and increasing the recovery factor; at 80 Under the conditions of ℃, NaCl concentration of 100000mg/L, and calcium and magnesium ion concentration of 500mg/L, the oil recovery rate is 39.15% higher than that of water flooding;
图4为实施例1-4制备得到的驱油用三相泡沫体系泡沫性能对比图;显然不同实施例中温度、矿化度以及配方含量不同,所得到泡沫性能不同,析液体积50mL所对应的时间即为析液半衰期,实施例1-4所对应的泡沫半衰期分别为34min、31min、25min、19min;Fig. 4 is the comparison chart of the foam properties of the three-phase foam system for oil displacement prepared in Examples 1-4; obviously, the temperature, salinity and formula content are different in different embodiments, and the obtained foam properties are different, and the liquid separation volume of 50mL corresponds to The time is the liquid analysis half-life, and the foam half-life corresponding to Embodiment 1-4 is respectively 34min, 31min, 25min, 19min;
图5为岩心驱替实验装置示意图。Fig. 5 is a schematic diagram of the core displacement experimental device.
具体实施方式Detailed ways
为使本发明的目的、技术方案和优点更加清楚,下面结合具体实施例和附图,对本发明的具体实施方式作进一步详细描述。In order to make the purpose, technical solution and advantages of the present invention clearer, the specific implementation manners of the present invention will be further described in detail below in conjunction with specific examples and accompanying drawings.
实施例1-4采用岩心驱替实验完成原油采收率的测定Embodiment 1-4 uses core displacement experiment to complete the determination of oil recovery
岩心驱替实验装置示意图如图5所示,具体试验步骤如下:The schematic diagram of the core displacement experiment device is shown in Figure 5, and the specific test steps are as follows:
(1)将所用岩心(渗透率200mD/1600mD非均质岩心)抽真空,随后饱和地层水。(1) Vacuumize the used core (heterogeneous core with a permeability of 200mD/1600mD), and then saturate it with formation water.
(2)恒温箱升温至实验温度,并使末端回压为大气压,环压设定为5MPa。(2) The temperature of the incubator is raised to the experimental temperature, and the back pressure at the end is atmospheric pressure, and the ring pressure is set at 5 MPa.
(3)对岩心进行饱和油,并在恒温箱中老化12h。(3) The core is saturated with oil, and aged in a constant temperature box for 12 hours.
(4)水驱1PV,CO2驱0.5PV,泡沫驱0.5PV,后续CO2驱0.5PV。(4) Water flooding 1PV, CO 2 flooding 0.5PV, foam flooding 0.5PV, and subsequent CO 2 flooding 0.5PV.
(5)泡沫驱采用泡沫发生器发泡,生成泡沫后注入岩心。(5) Foam flooding adopts a foam generator to foam, and injects the core after generating foam.
(6)依次水驱、CO2驱、泡沫驱、后续CO2驱。记录各个时刻的压力、产油量,产水量直至试验结束。(6) Water flooding, CO 2 flooding, foam flooding, and subsequent CO 2 flooding in sequence. Record the pressure, oil production and water production at each moment until the end of the test.
实施例1Example 1
步骤S1,将一定量的去离子水倒入烧杯中,向烧杯中加入无机盐,配制100000mg/LNaCl、钙镁离子浓度500mg/L的无机盐溶液;Step S1, pour a certain amount of deionized water into a beaker, add inorganic salt into the beaker, and prepare an inorganic salt solution with 100000 mg/L NaCl and 500 mg/L calcium and magnesium ion concentration;
步骤S2,将烧杯置于磁力搅拌器上,设定转速350r/min,向烧杯中加入0.5质量份的阴离子表面活性剂AOS,搅拌30min至完全溶解;Step S2, place the beaker on a magnetic stirrer, set the speed at 350r/min, add 0.5 parts by mass of anionic surfactant AOS to the beaker, and stir for 30 minutes until completely dissolved;
步骤S3,向烧杯中加入0.3质量份的两性离子表面活性剂CHSB,搅拌30min至完全溶解;Step S3, adding 0.3 parts by mass of zwitterionic surfactant CHSB to the beaker, stirring for 30 minutes until completely dissolved;
步骤S4,向烧杯中加入2.5质量份的分散剂钠土,搅拌30min使其充分悬浮;Step S4, adding 2.5 parts by mass of dispersant sodium soil into the beaker, stirring for 30 minutes to make it fully suspended;
步骤S5,向烧杯中加入5质量份的固相颗粒粉煤灰,搅拌30min使其充分悬浮;Step S5, adding 5 parts by mass of solid-phase particle fly ash to the beaker, stirring for 30 minutes to make it fully suspended;
步骤S6,将搅拌好的发泡液用保鲜膜封口,放在恒温箱中,以80℃老化48h;Step S6, sealing the stirred foaming solution with a plastic wrap, placing it in an incubator, and aging at 80°C for 48 hours;
步骤S7,将老化后的发泡液转移至高速搅拌器中,向其中通入CO2气体10min,设定转速8000r/min,搅拌时间2min。Step S7, transferring the aged foaming liquid to a high-speed stirrer, passing CO 2 gas into it for 10 min, setting the rotation speed at 8000 r/min, and stirring for 2 min.
100ml发泡液通过Blender-Waring法产生的泡沫体积350mL,半衰期为34min,在水驱、CO2气驱后,注入0.5PV泡沫再进行CO2气驱,最终原油采收率为70.78%,较水驱提高39.15%。100ml of foaming fluid produced by the Blender-Waring method has a foam volume of 350mL and a half-life of 34min. After water flooding and CO 2 gas flooding, 0.5PV foam is injected and then CO 2 gas flooding. The final oil recovery rate is 70.78%. Water flooding increased by 39.15%.
实施例2Example 2
步骤S1,将一定量的去离子水倒入烧杯中,根据实际要求向烧杯中加入无机盐,配制150000mg/L NaCl的无机盐溶液;Step S1, pouring a certain amount of deionized water into a beaker, adding inorganic salts to the beaker according to actual requirements, and preparing an inorganic salt solution of 150000 mg/L NaCl;
步骤S2,将烧杯置于磁力搅拌器上,设定转速350r/min,向烧杯中加入0.5质量份的阴离子表面活性剂SDBS,搅拌30min至完全溶解;Step S2, place the beaker on a magnetic stirrer, set the speed at 350r/min, add 0.5 parts by mass of anionic surfactant SDBS into the beaker, and stir for 30 minutes until completely dissolved;
步骤S3,向烧杯中加入0.3质量份的两性离子表面活性剂CHSB,搅拌30min至完全溶解;Step S3, adding 0.3 parts by mass of zwitterionic surfactant CHSB to the beaker, stirring for 30 minutes until completely dissolved;
步骤S4,向烧杯中加入2.5质量份的分散剂钠土,搅拌30min使其充分悬浮;Step S4, adding 2.5 parts by mass of dispersant sodium soil into the beaker, stirring for 30 minutes to make it fully suspended;
步骤S5,向烧杯中加入5质量份的固相颗粒粉煤灰,搅拌30min使其充分悬浮;Step S5, adding 5 parts by mass of solid-phase particle fly ash to the beaker, stirring for 30 minutes to make it fully suspended;
步骤S6,将搅拌好的发泡液用保鲜膜封口,放在恒温箱中,以80℃老化48h;Step S6, sealing the stirred foaming solution with a plastic wrap, placing it in an incubator, and aging at 80°C for 48 hours;
步骤S7,将老化后的发泡液转移至高速搅拌器中,向其中通入CO2气体10min,设定转速8000r/min,搅拌时间2min。Step S7, transferring the aged foaming liquid to a high-speed stirrer, passing CO 2 gas into it for 10 min, setting the rotation speed at 8000 r/min, and stirring for 2 min.
100ml发泡液通过Blender-Waring法产生的泡沫体积330mL,半衰期为31min,在水驱、CO2气驱后,注入0.5PV泡沫再进行CO2气驱,最终原油采收率为36.67%,较水驱提高36.67%。100ml of foaming fluid produced by the Blender-Waring method has a foam volume of 330mL and a half-life of 31min. After water flooding and CO 2 gas flooding, 0.5PV foam is injected and then CO 2 gas flooding, the final oil recovery rate is 36.67%, compared with Water flooding increased by 36.67%.
实施例3Example 3
步骤S1,将一定量的去离子水倒入烧杯中,根据实际要求向烧杯中加入无机盐,配制钙镁离子浓度5000mg/L溶液;Step S1, pour a certain amount of deionized water into the beaker, add inorganic salts into the beaker according to actual requirements, and prepare a solution with a calcium and magnesium ion concentration of 5000 mg/L;
步骤S2,将烧杯置于磁力搅拌器上,设定转速350r/min,向烧杯中加入0.5质量份的阴离子表面活性剂AOS,搅拌30min至完全溶解;Step S2, place the beaker on a magnetic stirrer, set the speed at 350r/min, add 0.5 parts by mass of anionic surfactant AOS to the beaker, and stir for 30 minutes until completely dissolved;
步骤S3,向烧杯中加入0.3质量份的两性离子表面活性剂CHSB,搅拌30min至完全溶解;Step S3, adding 0.3 parts by mass of zwitterionic surfactant CHSB to the beaker, stirring for 30 minutes until completely dissolved;
步骤S4,向烧杯中加入2.5质量份的分散剂钠土,搅拌30min使其充分悬浮;Step S4, adding 2.5 parts by mass of dispersant sodium soil into the beaker, stirring for 30 minutes to make it fully suspended;
步骤S5,向烧杯中加入5质量份的固相颗粒粉煤灰,搅拌30min使其充分悬浮;Step S5, adding 5 parts by mass of solid-phase particle fly ash to the beaker, stirring for 30 minutes to make it fully suspended;
步骤S6,将搅拌好的发泡液用保鲜膜封口,放在恒温箱中以80℃老化48h;Step S6, sealing the stirred foaming solution with a plastic wrap, and placing it in an incubator for aging at 80°C for 48 hours;
步骤S7,将老化后的发泡液转移至高速搅拌器中,向其中通入CO2气体10min,设定转速8000r/min,搅拌时间2min。Step S7, transferring the aged foaming liquid to a high-speed stirrer, passing CO 2 gas into it for 10 min, setting the rotation speed at 8000 r/min, and stirring for 2 min.
100ml发泡液通过Blender-Waring法产生的泡沫体积310mL,半衰期为25min,在水驱、CO2气驱后,注入0.5PV泡沫再进行CO2气驱,最终原油采收率为63.66%,较水驱提高32.52%。100ml of foaming fluid produced by the Blender-Waring method has a foam volume of 310mL and a half-life of 25min. After water flooding and CO 2 gas flooding, 0.5PV foam is injected and then CO 2 gas flooding. The final oil recovery rate is 63.66%, compared with Water flooding increased by 32.52%.
实施例4:Example 4:
步骤S1,将一定量的去离子水倒入烧杯中,根据实际要求向烧杯中加入无机盐,配制100000mg/L NaCl、钙镁离子浓度500mg/L的无机盐溶液;Step S1, pouring a certain amount of deionized water into a beaker, adding inorganic salts to the beaker according to actual requirements, and preparing an inorganic salt solution with 100000 mg/L NaCl and 500 mg/L calcium and magnesium ion concentration;
步骤S2,将烧杯置于磁力搅拌器上,设定转速350r/min,向烧杯中加入0.5质量份的阴离子表面活性剂AOS,搅拌30min至完全溶解;Step S2, place the beaker on a magnetic stirrer, set the speed at 350r/min, add 0.5 parts by mass of anionic surfactant AOS to the beaker, and stir for 30 minutes until completely dissolved;
步骤S3,向烧杯中加入0.3质量份的两性离子表面活性剂CHSB,搅拌30min至完全溶解;Step S3, adding 0.3 parts by mass of zwitterionic surfactant CHSB to the beaker, stirring for 30 minutes until completely dissolved;
步骤S4,向烧杯中加入2.5质量份的分散剂钠土,搅拌30min使其充分悬浮;Step S4, adding 2.5 parts by mass of dispersant sodium soil into the beaker, stirring for 30 minutes to make it fully suspended;
步骤S5,向烧杯中加入5质量份的固相颗粒粉煤灰,搅拌30min使其充分悬浮;Step S5, adding 5 parts by mass of solid-phase particle fly ash to the beaker, stirring for 30 minutes to make it fully suspended;
步骤S6,将搅拌好的发泡液用保鲜膜封口,放在恒温箱中,以120℃老化48h;Step S6, sealing the stirred foaming solution with a plastic wrap, placing it in an incubator, and aging it at 120°C for 48 hours;
步骤S7,将老化后的发泡液转移至高速搅拌器中,向其中通入CO2气体10min,设定转速8000r/min,搅拌时间2min。Step S7, transferring the aged foaming liquid to a high-speed stirrer, passing CO 2 gas into it for 10 min, setting the rotation speed at 8000 r/min, and stirring for 2 min.
100ml发泡液通过Blender-Waring法产生的泡沫体积320mL,半衰期为19min,在水驱、CO2气驱后,注入0.5PV泡沫再进行CO2气驱,最终原油采收率为60.82%,较水驱提高28.37%。100ml of foaming fluid produced by the Blender-Waring method has a volume of 320mL of foam and a half-life of 19 minutes. After water flooding and CO 2 gas flooding, 0.5PV foam is injected and then CO 2 gas flooding. The final oil recovery rate is 60.82%. Water flooding increased by 28.37%.
在不冲突的情况下,本文中上述实施例及实施例中的特征可以相互结合。In the case of no conflict, the above-mentioned embodiments and features in the embodiments herein may be combined with each other.
以上所述仅为本发明的较佳实施例,并不用以限制本发明,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. Any modifications, equivalent replacements, improvements, etc. made within the spirit and principles of the present invention shall be included in the protection of the present invention. within range.
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