Carbon dioxide injection and production well cementation cement paste as well as preparation method and application thereof
By introducing polymer emulsion and self-repair materials into the cementing cement slurry, the problems of traditional cement slurry being reduced in high carbon dioxide environments are solved, and higher corrosion resistance and self-repair capabilities are achieved, ensuring long-term stable sealing of oil and gas wells.
Patent Information
- Application Number
- CN202510496197.0
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Filing Date
- 2025-04-21
- Publication Date
- 2025-05-27
- Estimated Expiration
- 2045-04-21
AI Technical Summary
Traditional cementing cement slurry faces carbonization reaction in a high carbon dioxide environment, resulting in a decrease in pH value, a decrease in strength, an increase in permeability and a lack of self-repair function, making it difficult to meet the long-term stable sealing and support requirements of oil and gas wells.
By adjusting the formulation of cementing cement slurry, polymer emulsions and self-healing materials are introduced. The polymer emulsion prevents alkaline hydration products from being corroded by forming polymer film structures, and the self-healing materials repair microcracks through microbial mineralization reactions.
It improves the corrosion resistance and self-repair capability of cement slurry in high carbon dioxide environments, ensures the stability and sealing performance of cement rings, and reduces the risks and costs of oil well operation.
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Figure CN120040139A_ABST
Abstract
Description
Technical Field
[0001] The present invention belongs to the technical field of cementing cement, and particularly relates to a cement slurry for carbon dioxide injection and production wells, a preparation method thereof, and an application thereof. Background Art
[0002] In the process of oil and gas field development, cementing is one of the important processes to ensure the safe and stable operation of oil wells. The main function of the cement slurry for cementing is to fill the annular space between the casing and the wellbore wall, form an effective sealing layer, prevent the interflow of different formation fluids, and ensure the long-term stable production of oil wells. However, in oil and gas wells containing high-concentration carbon dioxide gas, traditional cement slurries for cementing face a series of severe challenges. Especially in recent years, more and more carbon dioxide enhanced oil recovery and storage (CCUS) projects have been carried out globally, including in China. The leakage problem of carbon dioxide along the cement sheath is an important risk point that cannot be ignored in the safe operation of such projects. The sealing safety of the cement slurry for cementing throughout the life cycle of CCUS projects has become one of the current hot issues of concern.
[0003] The existing cement slurries for cementing have the following main problems in an environment rich in carbon dioxide: Carbonation reaction: Carbon dioxide gas reacts with calcium hydroxide in the cement slurry to form calcium carbonate, resulting in a decrease in the pH value of the cement slurry and a weakening of the alkaline environment.
[0004] Strength reduction and permeability increase: The carbonation reaction not only reduces the pH value of the cement slurry but also weakens the stability of its internal structure, thereby affecting the strength and permeability of the cement sheath and causing sealing failure.
[0005] Lack of self-healing function: During the operation of CCUS projects in carbon dioxide injection and production wells, there are multiple up-and-down processes of pipe strings in the wellbore, which are extremely likely to impact the casing, generate microcracks in the cement sheath, and cause carbon dioxide to leak upward along the microcracks. Traditional cement slurries lack self-healing functions and cannot inhibit the expansion of cracks, further exacerbating the aging and damage of the material.
[0006] The combined action of these factors makes it difficult for traditional cement slurries for cementing to meet the long-term stable sealing and support requirements of oil and gas wells in a high-carbon dioxide environment, increasing the risks and costs of oil well operation.
[0007] "Self-healing microcapsule concrete capable of fixing carbon dioxide" with the application number CN107500589A discloses a self-healing microcapsule concrete, but it is mainly applied in the construction field, which has a large difference from the application scenarios and requirements in the oil exploration field. "Self-healing well cement slurry for use in medium and low temperatures and its application when encountering carbon dioxide" with the application number CN118026608A discloses a self-healing well cement slurry, but its core is to add slag, which will affect the strength of the well cement slurry to varying degrees and has relatively high requirements for the formulation debugging of the system. Summary of the Invention
[0008] In view of the defects of the prior art, the present invention provides a well cement slurry for carbon dioxide injection and production wells, which can not only solve the problems of reduced corrosion strength and lack of integrity of the cement sheath in carbon dioxide injection and production wells, but also endow the cement stone with self-healing ability when damaged by carbon dioxide channeling, seal the carbon dioxide gas channeling path, and provide a more reliable technical guarantee for well cementing in carbon dioxide injection and production wells. At the same time, the present invention also provides a preparation method and application of the well cement slurry for carbon dioxide injection and production wells.
[0009] A well cement slurry for carbon dioxide injection and production wells, by weight, comprises the following components: 95 - 105 parts of oil well cement, 44 - 48 parts of water, 4 - 6 parts of polymer emulsion, 4 - 6 parts of self-healing material, 1.5 - 2.5 parts of drag reducer, 0.5 - 1.5 parts of fluid loss reducer, and 0.2 - 0.8 parts of defoamer; Wherein, the polymer emulsion is an emulsion polymerized from methyl methacrylate, vinyltrimethoxysilane and propylene carbonate as monomers; The self-healing material is a microcapsule encapsulating Thiobacillus ferrooxidans cells and Bacillus amyloliquefaciens cells.
[0010] Preferably, the polymer emulsion is prepared by the following method: dispersing methyl methacrylate, vinyltrimethoxysilane and propylene carbonate in the dispersion medium water under the action of a dispersion aid, adjusting the pH to 7, then adding an initiator, and stirring and reacting at 55 - 60 °C for 7 - 8 h.
[0011] Preferably, the ratio of methyl methacrylate, vinyltrimethoxysilane, propylene carbonate, dispersion medium, dispersion aid, and initiator is (90 - 110) g : (45 - 55) g : (35 - 45) g : 400 mL : (0.8 - 1.2) g : (0.8 - 1.2) g.
[0012] More preferably, the mass ratio of methyl methacrylate, vinyltrimethoxysilane, and propylene carbonate is 100 : 50 : 40.
[0013] Preferably, the dispersion aid is sodium dodecylbenzenesulfonate and the initiator is potassium persulfate.
[0014] Preferably, the self-healing material is prepared by the following method: (1) Mix the Thiobacillus ferrooxidans cells and Bacillus amyloliquefaciens cells to obtain a mixed cell mass; (2) Mix the mixed cell mass with the sodium alginate solution and extrude it into a CaCl 2 solution to form calcium alginate gel beads. Let them stand for 30 min, and then add them to the carboxymethyl chitosan solution for curing to obtain the self-healing material.
[0015] Preferably, the concentration of the sodium alginate solution is 1.5 wt%, the concentration of the CaCl 2 solution is 2 wt%, the concentration of the carboxymethyl chitosan solution is 1 wt%, and the ratio of the mixed cell mass to the sodium alginate solution is 20 g: 1000 mL.
[0016] Preferably, the mass ratio of the Thiobacillus ferrooxidans cells to the Bacillus amyloliquefaciens cells is 1:2.
[0017] Preferably, the drag reducer is a small molecule polymer; the defoamer is a silicone; the fluid loss reducer is cellulose and its derivatives.
[0018] More preferably, the cement slurry for cementing carbon dioxide injection-production wells comprises the following components: 100 parts of oil well cement, 44 parts of water, 5 parts of polymer emulsion, 5 parts of self-healing material, 2 parts of drag reducer, 1 part of fluid loss reducer, and 0.5 part of defoamer.
[0019] More preferably, the Thiobacillus ferrooxidans cells and Bacillus amyloliquefaciens cells are respectively cultured from Thiobacillus ferrooxidans and Bacillus amyloliquefaciens according to their respective growth conditions.
[0020] The preparation method of the cement slurry for cementing carbon dioxide injection-production wells: After respectively preparing the polymer emulsion and the self-healing material, mix the oil well cement, water, polymer emulsion, self-healing material, drag reducer, fluid loss reducer, and defoamer and stir evenly.
[0021] The application of the cement slurry in the cementing operation of carbon dioxide injection-production wells: Apply the cement slurry to the cementing operation of carbon dioxide injection-production wells, and the temperature of the applied well section is not higher than 60°C.
[0022] The present invention improves the performance of cement slurry in multiple aspects by adjusting the formula of the well cementing slurry, introducing polymer emulsion and self-healing materials: the polymer emulsion cross-links and combines to form a structure that fills the particle pores and microvoids, making the cement slurry (stone) more dense; when the polymer emulsion is incorporated into the cement slurry, the emulsion forms a polymer film structure on the surface of the original hydration products, which can prevent the alkaline hydration products from being corroded and improve the anti-corrosion performance of the cement slurry in a high-carbon dioxide environment; by introducing propylene carbonate into the monomers for synthesizing the polymer emulsion, the performance of the polymer is improved, the bonding strength with the cement hydration products is enhanced, and its stability is improved; a self-healing material that can resist the crossflow damage in carbon dioxide injection and production wells is introduced to ensure that the cement slurry can automatically repair microcracks when damaged by carbon dioxide injection and production.
[0023] Advantages of the present invention: The well cementing slurry provided by the present invention maintains good strength and low permeability in a carbon dioxide environment and has good anti-corrosion performance. It not only solves the stability problem of the well cementing annulus in the complex and harsh downhole environment of carbon dioxide injection and production wells, but also endows the cement slurry with self-healing ability under carbon dioxide injection and production conditions, providing a more reliable technical guarantee for the integrity of carbon dioxide injection and production wells. Description of the drawings
[0024] Figure 1 It is a test result diagram of the initial compressive strength of the cement stone for each experimental group; Figure 2 It is a test result diagram of the initial permeability of the cement stone for each experimental group. Detailed implementation manners
[0025] The oil well cement used in the present invention is G-class oil well cement, purchased from Jiahua Special Cement Co., Ltd.; Acidithiobacillus ferrooxidans is purchased from Mingzhou Biology, and the strain number is B80698; Bacillus amyloliquefaciens is purchased from Taisituo Biology, and the strain number is TS335151; Sarcina pasteurii is Sarcina pasteurii ATCC11859 of the American Type Culture Collection (ATCC); The drag reducer and fluid loss reducer are purchased from Weihui Chemical Industry Co., Ltd., and the models are GD-1 and G301 respectively; the defoamer is purchased from BASF SE of Germany, and the model is FoamStar A 38.
[0026] Example 1 A well cementing slurry for carbon dioxide injection and production wells is composed of the following raw materials: 100 g of oil well cement, 44 g of water, 5 g of polymer emulsion, 5 g of self-healing material, 2 g of drag reducer, 1 g of fluid loss reducer, and 0.5 g of defoamer; Among them, the polymer emulsion is prepared by the following method: 100 g of methyl methacrylate, 50 g of vinyltrimethoxysilane, 40 g of propylene carbonate, and 1 g of sodium dodecylbenzenesulfonate are dispersed in 400 mL of water, the pH is adjusted to 7.0, then 1 g of initiator potassium persulfate is added, and the mixture is stirred and reacted at 55 °C for 8 h; The self-healing material is prepared by the following method: (a) Thiobacillus ferrooxidans is inoculated into MRS liquid medium and fermented and cultured at 30 °C and 160 rpm for 48 h, and then the cells of Thiobacillus ferrooxidans are obtained by centrifugation; Bacillus amyloliquefaciens is inoculated into LB liquid medium and fermented and cultured at 37 °C and 150 rpm for 36 h, and then the cells of Bacillus amyloliquefaciens are obtained by centrifugation; The cells of Thiobacillus ferrooxidans and the cells of Bacillus amyloliquefaciens are mixed evenly according to a mass ratio of 1:2 to obtain a mixed cell mass; (b) Weigh 10.0 g of the mixed cell mass and mix it evenly with 500 mL of a 1.5 wt% sodium alginate solution, and use a sterile syringe to inject it into 2000 mL of a 2 wt% CaCl 2 solution to form calcium alginate gel beads. After standing and curing for 30 min, the gel beads are transferred to 1000 mL of a 1 wt% carboxymethyl chitosan solution for curing to obtain microcapsules, which are the self-healing material.
[0027] Mix the oil well cement, water, polymer emulsion, self-healing material, drag reducer, fluid loss agent, and defoamer, and stir evenly to prepare the cement slurry for cementing carbon dioxide injection and production wells.
[0028] Example 2 A cement slurry for cementing carbon dioxide injection and production wells is composed of the following raw materials: 105 g of oil well cement, 48 g of water, 4 g of polymer emulsion, 6 g of self-healing material, 1.5 g of drag reducer, 1.5 g of fluid loss agent, and 0.2 g of defoamer; Among them, the polymer emulsion is prepared by the following method: 110 g of methyl methacrylate, 45 g of vinyltrimethoxysilane, 45 g of propylene carbonate, and 1.2 g of sodium dodecylbenzenesulfonate are dispersed in 400 mL of water, the pH is adjusted to 7.0, then 1.2 g of initiator potassium persulfate is added, and the mixture is stirred and reacted at 60 °C for 7 h; The self-healing material is the same as that in Example 1.
[0029] All the raw materials are mixed and stirred evenly to prepare the cement slurry for cementing carbon dioxide injection and production wells.
[0030] Example 3 A cement slurry for cementing carbon dioxide injection-production wells is composed of the following raw materials: 95 g of oil well cement, 45 g of water, 6 g of polymer emulsion, 4 g of self-healing material, 2.5 g of drag reducer, 0.5 g of fluid loss reducer, and 0.8 g of defoamer; Among them, the polymer emulsion is prepared by the following method: 90 g of methyl methacrylate, 55 g of vinyltrimethoxysilane, 35 g of propylene carbonate, and 0.8 g of sodium dodecylbenzenesulfonate are dispersed in 400 mL of water, the pH is adjusted to 7.0, then 0.8 g of initiator potassium persulfate is added, and the mixture is stirred and reacted at 55 °C for 8 h; The self-healing material is the same as that in Example 1.
[0031] All the raw materials are mixed and stirred evenly to prepare the cement slurry for cementing carbon dioxide injection-production wells.
[0032] Comparative Example 1 When synthesizing the polymer emulsion, propylene carbonate is replaced by acrylamide, and the others are the same as in Example 1.
[0033] Comparative Example 2 In the self-healing material, Bacillus amyloliquefaciens cells are replaced by Sarcina pasteurii cells, and the others are the same as in Example 1; Among them, the cultivation process of Sarcina pasteurii cells is as follows: Sarcina pasteurii is inoculated into a urea medium (containing 20 g / L urea, 5 g / L ammonium chloride, 1 g / L yeast extract, 75 mmol / L tris buffer, pH 9.0), and fermented and cultured at 30 °C and 100 rpm for 72 h, and then Sarcina pasteurii cells are obtained by centrifugation.
[0034] Comparative Example 3 The self-healing material is prepared by the following method: (a) Thiobacillus ferrooxidans is inoculated into MRS liquid medium and fermented and cultured at 30 °C and 160 rpm for 48 h, and then Thiobacillus ferrooxidans cells are obtained by centrifugation; (b) Weigh 10.0 g of Thiobacillus ferrooxidans cells and mix them evenly with 500 mL of 1.5 wt% sodium alginate solution. Use a sterile syringe to inject it into 2000 mL of 2 wt% CaCl 2 solution to form calcium alginate gel beads. After standing and curing for 30 min, transfer the gel beads to 1000 mL of 1 wt% carboxymethyl chitosan solution for curing to obtain microcapsules, which are the self-healing material; The others are the same as in Example 1.
[0035] Comparative Example 4 The self-healing material is prepared by the following method: (a) Inoculate Bacillus amyloliquefaciens into LB liquid medium and ferment it at 37 °C and 150 rpm for 36 h. Then, centrifuge to obtain Bacillus amyloliquefaciens cells. (b) Weigh 10.0 g of Bacillus amyloliquefaciens cells and mix them evenly with 500 mL of a 1.5 wt% sodium alginate solution. Use a sterile syringe to inject the mixture into 2000 mL of a 2 wt% CaCl 2 solution to form calcium alginate gel beads. After standing and curing for 30 min, transfer the gel beads to 1000 mL of a 1 wt% carboxymethyl chitosan solution for curing to obtain microcapsules, which are self-healing materials.
[0036] Others are the same as in Example 1.
[0037] Comparative Example 5 Do not add polymer emulsion and self-healing material, and others are the same as in Example 1.
[0038] Comparative Example 6 Do not add self-healing material, and others are the same as in Example 1.
[0039] Comparative Example 7 Do not add polymer emulsion, and others are the same as in Example 1.
[0040] Performance testing Prepare cement stones from the well cement slurries provided in Examples 1-5 and Comparative Examples 1-7 above (referring to the method of GB / T19139-2012), and detect the initial compressive strength and permeability. Then, place the prepared cement stones under a carbon dioxide pressure of 6 MPa and conduct a corrosion experiment at 50 °C. Evaluate the corrosion degree of the cement stones after 28 days of corrosion. The corrosion device is an XWL-18 type high-temperature and high-pressure carbon dioxide reaction kettle; The corrosion degree of the cement stone is mainly evaluated according to the corrosion depth, compressive strength decay rate, and permeability increase rate. The specific evaluation method for the corrosion depth of the cement stone is as follows: Take out the cement stone that has been corroded for a certain time under the experimental conditions, cut it in half, and evenly apply phenolphthalein reagent to the section. The hydration products of the cement stone are alkaline and will turn red when encountering phenolphthalein. However, the alkalinity of the hydrated products of the cement stone corroded by acidic corrosion medium will weaken or even become neutral, and it will not change color or turn light red when encountering phenolphthalein. Finally, use a vernier caliper to measure the thickness of multiple places without red at the boundary, and the average value of the measurement results is the corrosion depth of the cement stone (hereinafter referred to as the corrosion depth); The compressive strength tested after the curing of the hardened cement paste is taken as the initial compressive strength, and the compressive strength after a certain period of corrosion is taken as the compressive strength after corrosion. The compressive strength is tested using a YJ-2001 uniformly loaded pressure testing machine, and the curing of the hardened cement paste is carried out using a DFC-0722 type pressurized curing autoclave. The greater the decay rate of the compressive strength, the more severe the corrosion degree of the hardened cement paste. The calculation formula for the decay rate of the compressive strength is as follows: α = (P - P i ) / P × 100%; In the formula, α is the decay rate of the compressive strength, with the unit of %; P is the initial compressive strength, with the unit of MPa; P i is the compressive strength after the i-th day of corrosion, with the unit of MPa; The permeability tested after the curing of the hardened cement paste is taken as the initial permeability, and the permeability after a certain period of corrosion of the hardened cement paste is taken as the permeability after corrosion. The permeability is tested using a CMS300 type computer-controlled automatic testing system for confining pressure porosity and permeability. The greater the increase rate of the permeability, the greater the corrosion degree of the hardened cement paste. The calculation formula for the change rate of the permeability is as follows: μ = (K i - K) / K × 100%; In the formula, μ is the change rate of the permeability, with the unit of %; K is the initial permeability, with the unit of mD; K i is the permeability after the i-th day of corrosion, with the unit of mD; The self-healing effect of the hardened cement paste is evaluated through the self-healing efficiency. The specific process is as follows: First, a cylindrical specimen is loaded with a pressure of 20 MPa using a pressure testing machine, and the volume of the internal cracks is measured using a CT scanner (model METROTOM1) and calibrated as the original crack volume. Then, the sample is placed in a high-temperature and high-pressure carbon dioxide reaction autoclave. After a certain period of corrosion, it is taken out, and the volume of the internal cracks is measured again using a CT scanner and calibrated as the crack volume after repair. The difference between the two crack volumes divided by the original crack volume is the self-healing efficiency. The calculation formula for the self-healing efficiency is as follows: β = (V - V i ) / V × 100%; In the formula, β is the self-healing efficiency, with the unit of %; V is the initial crack volume, with the unit of mm 3 ; V i is the crack volume after repair after the i-th day of corrosion, with the unit of mm 3 ; In the present invention, the tested P i , K i , V i are respectively the P 28 , K 28 , V 28 after 28 days. The test results of the initial compressive strength and initial permeability of the hardened cement paste in each experimental group are shown inFigure 1 and Figure 2 , and the relevant corrosion detection results are shown in Table 1; Table 1 Corrosion depth, compressive strength decay rate, permeability increase rate and self - repair efficiency of each cement stone Example / Comparative Example Corrosion depth (cm) Compressive strength decay rate (%) Permeability increase rate (%) Self-healing efficiency (%) Example 1 0.31 3.31 5.10 76.79 Example 2 0.35 4.24 5.64 76.23 Example 3 0.43 4.85 6.05 71.26 Comparative Example 1 1.46 16.20 15.24 56.37 Comparative Example 2 1.25 12.23 13.09 42.33 Comparative Example 3 1.18 11.49 12.56 39.34 Comparative Example 4 1.26 13.58 13.72 37.89 Comparative Example 5 1.74 25.27 21.85 11.62 Comparative Example 6 1.32 14.65 14.34 15.34 Comparative Example 7 1.56 18.68 18.32 51.23
[0041] It can be seen from Figure 1 and Figure 2 that after introducing the polymer emulsion and the self - repair material in the present invention, the compressive strength of the cement stone has been improved to a certain extent, and the permeability has been reduced; It can be seen from Table 1 that by introducing the polymer emulsion and the self - repair material, the present invention effectively improves the corrosion resistance of the well - cementing cement. Moreover, the selected polymer monomer combination of methyl methacrylate, vinyltrimethoxysilane and propylene carbonate in the present invention has its particularity, which can effectively improve the physical properties of the polymer and enhance its carbon dioxide resistance. Through the polymer macromolecular cross - linking and bonding structure to fill the particle pores and micro - pores, the cement slurry system can be made more dense; when the polymer emulsion is incorporated into the cement slurry, the emulsion forms a polymer film structure on the surface of the original hydration products, which can prevent the alkaline hydration products from being corroded and improve the anti - corrosion performance of the cement slurry in a high - carbon - dioxide environment. By introducing propylene carbonate, the performance of the polymer emulsion is improved, the bonding strength with the cement hydration products is enhanced, and its stability is improved. Combining the compressive strength and anti - corrosion evaluation results of Example 1 and Comparative Example 1, it can be seen that the propylene carbonate monomer plays an important role in improving the physical properties and anti - corrosion properties of the cement; The present invention also combines Thiobacillus ferrooxidans and Bacillus amyloliquefaciens, and through the mineralization reaction of microorganisms, bio - repair is carried out on the cement cracks caused by gas channeling during the carbon dioxide injection and production process. Using the two strains alone is difficult to achieve the effect of combined use. Moreover, although both Bacillus amyloliquefaciens and Sarcina pasteurii have the property of producing urease, after replacing Bacillus amyloliquefaciens with Sarcina pasteurii, the corrosion resistance and self - repair performance of the cement show a significant downward trend. Based on the above, the present invention believes that Thiobacillus ferrooxidans and Bacillus amyloliquefaciens produce a certain synergistic effect during bio - repair.
[0042] It can be seen from the above test results that when adding the polymer emulsion alone or adding the self - repair material alone, the anti - corrosion effect of the cement stone is weaker than the overall scheme of the present invention. This is mainly because the synergistic effect of the two materials is strong. The polymer emulsion of the present invention can limit the expansion of cracks, making the crack scale within the effective range where the self - repair material can act efficiently, and the overall anti - corrosion effect is better.
Claims
1. A cement slurry for carbon dioxide injection and production well cementing, characterized in that: By weight, it includes the following components: 95-105 parts of oil well cement, 44-48 parts of water, 4-6 parts of polymer emulsion, 4-6 parts of self-repairing material, 1.5-2.5 parts of drag reducer, 0.5-1.5 parts of fluid loss reducer and 0.2-0.8 parts of defoamer; Wherein, the polymer emulsion is an emulsion polymerized with methyl methacrylate, vinyl trimethoxy silane and propylene carbonate as monomers; The self-repairing material is a microcapsule that encapsulates the cells of Thiobacillus ferrooxidans and the cells of Bacillus amyloliquefaciens.
2. The carbon dioxide injection and production well cementing slurry according to claim 1, characterized in that: The polymer emulsion is prepared by the following method: methyl methacrylate, vinyl trimethoxysilane and propylene carbonate are dispersed in a dispersion medium of water under the action of a dispersing aid, the pH is adjusted to 7, an initiator is added, and the reaction is stirred at 55-60° C. for 7-8 hours.
3. The carbon dioxide injection and production well cementing slurry according to claim 2, characterized in that: The ratio of methyl methacrylate, vinyl trimethoxysilane, propylene carbonate, dispersion medium, dispersion aid and initiator is (90-110) g: (45-55) g: (35-45) g: 400 mL: (0.8-1.2) g: (0.8-1.2) g.
4. The carbon dioxide injection and production well cementing slurry according to claim 3, characterized in that: The dispersing aid is sodium dodecylbenzene sulfonate, and the initiator is potassium persulfate.
5. The carbon dioxide injection and production well cementing slurry according to claim 1, characterized in that: The self-healing material is prepared by the following method: (1) mixing Thiobacillus ferrooxidans cells and Bacillus amyloliquefaciens cells to obtain a mixed cell; (2) The mixed bacteria and sodium alginate solution are mixed, squeezed into a CaCl2 solution to form calcium alginate gel beads, left to stand for 30 minutes, and then added into a carboxymethyl chitosan solution for solidification to obtain the self-healing material.
6. The carbon dioxide injection and production well cementing slurry according to claim 5, characterized in that: The concentration of the sodium alginate solution is 1.5wt%, the concentration of the CaCl2 solution is 2wt%, the concentration of the carboxymethyl chitosan solution is 1wt%, and the ratio of the mixed bacteria to the sodium alginate solution is 20g:1000mL.
7. The carbon dioxide injection and production well cementing slurry according to claim 5, characterized in that: The mass ratio of the Thiobacillus ferrooxidans cells to the Bacillus amyloliquefaciens cells is 1:
2.
8. The carbon dioxide injection and production well cementing slurry according to claim 1, characterized in that: The drag reducer is a small molecule polymer; the defoamer is an organosilicon; and the fluid loss reducer is cellulose and its derivatives.
9. The method for preparing the carbon dioxide injection and production well cementing slurry according to claim 1, characterized in that: After the polymer emulsion and the self-repairing material are prepared respectively, the oil well cement, water, the polymer emulsion, the self-repairing material, the drag reducer, the fluid loss reducer and the defoaming agent are mixed and stirred evenly.
10. The application of the cementing slurry according to claim 1 in the cementing operation of carbon dioxide injection and production wells, characterized in that: The application well section temperature of the cementing slurry is not higher than 60°C.
Citation Information
Patent Citations
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