CN113090241A - Acid fracturing method for carbonate reservoir - Google Patents

Acid fracturing method for carbonate reservoir Download PDF

Info

Publication number
CN113090241A
CN113090241A CN202010017020.5A CN202010017020A CN113090241A CN 113090241 A CN113090241 A CN 113090241A CN 202010017020 A CN202010017020 A CN 202010017020A CN 113090241 A CN113090241 A CN 113090241A
Authority
CN
China
Prior art keywords
acid
percent
fracturing
dosage
target layer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN202010017020.5A
Other languages
Chinese (zh)
Inventor
王津建
闫阳
田福春
郭树召
杨扬
闫钰
蔡晴琴
李庆华
韩晶玉
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Petrochina Co Ltd
Original Assignee
Petrochina Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Petrochina Co Ltd filed Critical Petrochina Co Ltd
Priority to CN202010017020.5A priority Critical patent/CN113090241A/en
Publication of CN113090241A publication Critical patent/CN113090241A/en
Pending legal-status Critical Current

Links

Classifications

    • EFIXED CONSTRUCTIONS
    • E21EARTH DRILLING; MINING
    • E21BEARTH DRILLING, e.g. DEEP DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
    • E21B43/00Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
    • E21B43/25Methods for stimulating production
    • E21B43/26Methods for stimulating production by forming crevices or fractures
    • 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
    • C09K8/60Compositions for stimulating production by acting on the underground formation
    • C09K8/62Compositions for forming crevices or fractures
    • C09K8/72Eroding chemicals, e.g. acids
    • C09K8/74Eroding chemicals, e.g. acids combined with additives added for specific purposes

Abstract

The invention discloses an acid fracturing method for a carbonate reservoir, and belongs to the field of oil and gas development. The method comprises the following steps: injecting acid fracturing fluid into the shaft to a target layer through the oil pipe and/or the oil sleeve annulus; and closing the well for setting time to finish acid fracturing. The acid fracturing fluid comprises: resistance reducing liquid, gelled acid, cross-linked acid, diverting acid and closed acid; injecting an acid fracturing fluid into a wellbore comprises: and injecting the resistance reducing liquid, the cross-linking acid, the gelled acid, the diverting acid, the resistance reducing liquid, the cross-linking acid, the gelled acid, the closed acid and the resistance reducing liquid to the target layer in the same application amount into the shaft in sequence. The method provided by the embodiment of the invention can be used for deep fracturing, is beneficial to forming complex cracks, effectively improves the formation permeability, obviously improves the crack flow conductivity and widens the crude oil flow channel.

Description

Acid fracturing method for carbonate reservoir
Technical Field
The invention relates to the field of oil and gas development, in particular to an acid fracturing method for a carbonate reservoir.
Background
Carbonate reservoirs, especially buried carbonate reservoirs in the mountains, have abundant oil and gas resources, strong reservoir heterogeneity, deep reservoir burial depth (for example, the burial depth is 3900-4500 m), high stress, high reservoir temperature (for example, 150-180 ℃), and short effective acting distance of acid liquor. The buried depth of the buried hill production zone peak group and the Majiagou group is 3900-4500m, and the formation temperature is 150-180 ℃, so in order to improve the productivity, reservoir transformation is needed.
At present, the method for modifying carbonate reservoirs mainly comprises the following steps: the multistage injection acid fracturing technology is characterized in that the pad fluid and the acid fluid are alternately injected, and the filtration rate of the acid fluid is lower than that of the acid injected at the upper stage, and meanwhile, the acid fluid forms fingering in the pad fluid for multiple times, so that more cracks are favorably formed. The closed acid fracturing technology utilizes acid liquor to etch the stratum in the existing natural cracks or partially closed cracks, improves the stratum permeability and communicates the stratum cracks.
In the process of implementing the invention, the inventor finds that at least the following problems exist in the prior art:
the multi-stage injection acid fracturing technology has the problems of high acid rock reaction rate and small treatment range, the closed acid fracturing technology is not beneficial to forming complex cracks, and the improvement on the flow conductivity of cracks in a near well zone is very limited.
Disclosure of Invention
In view of the above, the invention provides an acid fracturing method for a carbonate reservoir, which can perform deep fracturing, is beneficial to forming complex cracks and improves the flow conductivity of the cracks.
An acid fracturing method of a carbonate reservoir, the acid fracturing method comprising: injecting acid fracturing fluid into the shaft to a target layer through the oil pipe and/or the oil sleeve annulus;
closing the well for setting time to finish acid fracturing;
wherein the acid fracturing fluid comprises: resistance reducing liquid, gelled acid, cross-linked acid, diverting acid and closed acid;
the step of injecting the acid fracturing fluid into the well bore comprises the following steps in sequence: injecting the resistance reducing fluid into the shaft to a target layer according to the first dosage;
continuing to inject the crosslinking acid into the wellbore to the target zone according to the second dosage;
according to a third dosage, continuously injecting the gelled acid into the shaft until the target layer is formed;
according to a fourth dosage, continuing to inject the diverting acid into the well bore to the target layer;
according to a fifth dosage, continuing to inject the resistance reducing fluid into the shaft until the target layer is reached;
continuing to inject the crosslinking acid into the wellbore to the target zone according to a sixth dosage;
according to a seventh dosage, continuing to inject the gelled acid into the well bore to the target layer;
continuing to inject the closure acid into the wellbore to the zone of interest at an eighth dosage below fracture closure pressure;
and continuing to inject the resistance reducing fluid into the well bore to the target layer according to a ninth dosage under the condition of lower than the fracture closing pressure.
In one possible implementation manner, the resistance reducing liquid comprises the following components in percentage by mass: 0.5-1% of resistance reducing agent and the balance of water.
In one possible implementation manner, the gelling acid comprises the following components in percentage by mass: 10 to 20 percent of industrial synthetic hydrochloric acid, 10 to 15 percent of gelling agent for acidification, 2 to 5 percent of corrosion inhibitor, 2 to 5 percent of iron ion stabilizer, 2 to 5 percent of cleanup additive, 2 to 5 percent of wetting agent for oil recovery, 1 to 3 percent of clay stabilizer and the balance of water.
In one possible implementation manner, the crosslinking acid comprises the following components in percentage by mass: 10 to 20 percent of industrial synthetic hydrochloric acid, 0.2 to 0.5 percent of crosslinking acid liquid conditioner for acidification, 0.5 to 1 percent of crosslinking acid thickener for acidification, 3 to 8 percent of high-temperature corrosion inhibitor, 3 to 8 percent of wetting agent for oil extraction, 2 to 5 percent of cleanup additive for fracturing, 2 to 5 percent of iron ion stabilizer, 2 to 5 percent of clay stabilizer and the balance of water.
In one possible implementation manner, the diverting acid comprises the following components in percentage by mass: 10 to 30 percent of industrial synthetic hydrochloric acid, 3 to 8 percent of high-temperature corrosion inhibitor, 3 to 8 percent of self-steering agent for acidification, 3 to 8 percent of wetting agent for oil extraction, 2 to 5 percent of cleanup additive for fracturing, 2 to 5 percent of iron ion stabilizer, 2 to 5 percent of clay stabilizer and the balance of water.
In one possible implementation manner, the closed acid comprises the following components in percentage by mass: 10 to 30 percent of industrial synthetic hydrochloric acid, 3 to 8 percent of high-temperature corrosion inhibitor, 3 to 8 percent of wetting agent for oil extraction, 2 to 5 percent of cleanup additive for fracturing, 2 to 5 percent of iron ion stabilizer, 2 to 5 percent of clay stabilizer and the balance of water.
In a possible implementation manner, for the resistance reducing liquid, the first dosage is 200m3-1000m3The fifth dosage is 200m3-500m3The ninth dosage is 20m3-80m3
In one possible implementation, for the crosslinking acid, the second amount is 100m3-300m3The sixth dosage is 100m3-300m3
In one possible implementation, for the gelling acid, the third amount is 300m3-500m3The seventh dosage is 100m3-300m3
In one possible implementation, for the diverting acid, the fourth amount is 200m3-300m3
For the blocking acid, the eighth amount is 20m3-80m3
The technical scheme provided by the embodiment of the invention has the beneficial effects that at least:
according to the acid fracturing method provided by the embodiment of the invention, specific types of acid fracturing fluids are sequentially injected into a shaft to perform deep fracturing by aiming at the characteristics of carbonate reservoirs, particularly high-temperature carbonate reservoirs in a buried hill, and complex fractures are formed at the same time. Specifically, a resistance reducing fluid is injected into the shaft to a target layer for resistance reduction, the temperature of the shaft is reduced, and the reaction rate of acid rock is slowed down, so that the acid corrosion crack length is increased, and the acid corrosion range is enlarged. And then continuously injecting the crosslinking acid into the well bore to the target layer to perform seam making. And then continuously injecting gelled acid into the shaft to the target layer so as to deeply etch the crack. And then, continuously injecting steering acid into the shaft to a target layer so as to perform temporary blocking in the formed artificial cracks, improving the net pressure in the cracks, forcing the artificial cracks to form a plurality of branch cracks to realize interlayer steering, and improving the complexity of the cracks. And then, continuously injecting resistance reducing fluid, cross-linking acid and gelling acid into the shaft to a target layer so as to further deepen the branch cracks, communicate and prolong the stratum cracks, realize deep fracturing and form complex cracks. And finally, injecting a resistance reducing fluid into the shaft under the pressure lower than the fracture closure pressure so as to push the acid fracturing fluid in the shaft into the deep part of the stratum, dredging the existing fracture and further optimizing the acid fracturing effect. Therefore, the method provided by the embodiment of the invention can be used for deep fracturing, is beneficial to forming complex cracks, effectively improves the formation permeability, obviously improves the crack flow conductivity and widens the crude oil flow channel.
Detailed Description
In order to make the technical solutions and advantages of the present invention more clear, embodiments of the present invention will be described in further detail below.
The embodiment of the invention provides an acid fracturing method of a carbonate reservoir, which comprises the following steps: injecting acid fracturing fluid into the shaft to a target layer through the oil pipe and/or the oil sleeve annulus;
and closing the well for setting time to finish acid fracturing.
Wherein, the acid fracturing fluid comprises: resistance reducing liquid, gelled acid, cross-linking acid, diverting acid and closed acid.
Injecting the acid fracturing fluid into the wellbore comprises the following steps in sequence: injecting resistance reducing liquid into the shaft to a target layer according to the first dosage;
according to the second dosage, continuously injecting the cross-linking acid into the shaft to the target layer;
according to the third dosage, continuously injecting gelled acid into the shaft until the target layer is reached;
according to the fourth dosage, continuously injecting diverting acid into the shaft to the target layer;
according to the fifth dosage, continuously injecting resistance reducing liquid into the shaft to a target layer;
according to the sixth dosage, continuously injecting the crosslinking acid into the shaft to the target layer;
according to the seventh dosage, continuously injecting gelled acid into the shaft to a target layer;
under the condition that the pressure is lower than the fracture closure pressure, according to the eighth dosage, continuing to inject closure acid into the shaft to a target layer;
and under the condition of being lower than the fracture closing pressure, continuously injecting the resistance reducing liquid into the shaft to the target layer according to the ninth dosage.
According to the acid fracturing method provided by the embodiment of the invention, specific types of acid fracturing fluids are sequentially injected into a shaft to perform deep fracturing by aiming at the characteristics of carbonate reservoirs, particularly high-temperature carbonate reservoirs in a buried hill, and complex fractures are formed at the same time. Specifically, a resistance reducing fluid is injected into the shaft to a target layer for resistance reduction, the temperature of the shaft is reduced, and the reaction rate of acid rock is slowed down, so that the acid corrosion crack length is increased, and the acid corrosion range is enlarged. And then continuously injecting the crosslinking acid into the well bore to the target layer to perform seam making. And then continuously injecting gelled acid into the shaft to the target layer so as to deeply etch the crack. And then, continuously injecting steering acid into the shaft to a target layer so as to perform temporary blocking in the formed artificial cracks, improving the net pressure in the cracks, forcing the artificial cracks to form a plurality of branch cracks to realize interlayer steering, and improving the complexity of the cracks. And then, continuously injecting resistance reducing fluid, cross-linking acid and gelling acid into the shaft to a target layer so as to further deepen the branch cracks, communicate and prolong the stratum cracks, realize deep fracturing and form complex cracks. And finally, injecting a resistance reducing fluid into the shaft under the pressure lower than the fracture closure pressure so as to push the acid fracturing fluid in the shaft into the deep part of the stratum, dredging the existing fracture and further optimizing the acid fracturing effect. Therefore, the method provided by the embodiment of the invention can be used for deep fracturing, is beneficial to forming complex cracks, effectively improves the formation permeability, obviously improves the crack flow conductivity and widens the crude oil flow channel.
Aiming at the characteristic that the reservoir temperature of the acid salt rock reservoir, particularly the buried hill carbonate reservoir is high (for example, 150-180 ℃), various acid fracturing fluids with high temperature resistance are selected in the embodiment of the invention, the temperature resistance can reach more than 180 ℃, and the various acid fracturing fluids are exemplified as follows:
as an example, the resistance-reducing liquid comprises the following components in percentage by mass: 0.5-1% of resistance reducing agent and the balance of water. For example, the mass percent of the friction reducer may be 0.8%.
The resistance reducer can adopt the resistance reducer modified polymer GC-212L for fracture acidizing, which is commonly used in the field.
As an example, the gelled acid comprises the following components in percentage by mass: 10 to 20 percent of industrial synthetic hydrochloric acid, 10 to 15 percent of gelling agent for acidification, 2 to 5 percent of corrosion inhibitor, 2 to 5 percent of iron ion stabilizer, 2 to 5 percent of cleanup additive, 2 to 5 percent of wetting agent for oil recovery, 1 to 3 percent of clay stabilizer and the balance of water.
Preferably, the gelling acid comprises the following components in percentage by mass: 15% of industrial synthetic hydrochloric acid, 10% of gelling agent for acidification, 3% of corrosion inhibitor, 3% of iron ion stabilizer, 3% of cleanup additive, 3% of wetting agent for oil recovery, 2% of clay stabilizer and the balance of water.
As an example, the cross-linking acid comprises the following components in percentage by mass: 10 to 20 percent of industrial synthetic hydrochloric acid, 0.2 to 0.5 percent of crosslinking acid liquid conditioner for acidification, 0.5 to 1 percent of crosslinking acid thickener for acidification, 3 to 8 percent of high-temperature corrosion inhibitor, 3 to 8 percent of wetting agent for oil extraction, 2 to 5 percent of cleanup additive for fracturing, 2 to 5 percent of iron ion stabilizer, 2 to 5 percent of clay stabilizer and the balance of water.
Preferably, the crosslinking acid comprises the following components in percentage by mass: 20 percent of industrial synthetic hydrochloric acid, 0.4 percent of cross-linked acid liquid conditioner for acidification, 0.8 percent of cross-linked acid thickener for acidification, 5 percent of high-temperature corrosion inhibitor, 3 percent of wetting agent for oil extraction, 3 percent of cleanup additive for fracturing, 3 percent of iron ion stabilizer, 2 percent of clay stabilizer and the balance of water.
As an example, the diverting acid comprises the following components in percentage by mass: 10 to 30 percent of industrial synthetic hydrochloric acid, 3 to 8 percent of high-temperature corrosion inhibitor, 3 to 8 percent of self-steering agent for acidification, 3 to 8 percent of wetting agent for oil extraction, 2 to 5 percent of cleanup additive for fracturing, 2 to 5 percent of iron ion stabilizer, 2 to 5 percent of clay stabilizer and the balance of water.
Preferably, the diverting acid comprises the following components in percentage by mass: 20% of industrial synthetic hydrochloric acid, 5% of high-temperature corrosion inhibitor, 5% of self-diverting agent for acidification, 5% of wetting agent for oil recovery, 3% of cleanup additive for fracturing, 3% of iron ion stabilizer, 2% of clay stabilizer and the balance of water.
As an example, the closed acid comprises the following components in percentage by mass: 10 to 30 percent of industrial synthetic hydrochloric acid, 3 to 8 percent of high-temperature corrosion inhibitor, 3 to 8 percent of wetting agent for oil extraction, 2 to 5 percent of cleanup additive for fracturing, 2 to 5 percent of iron ion stabilizer, 2 to 5 percent of clay stabilizer and the balance of water.
Preferably, the closed acid comprises the following components in percentage by mass: 20% of industrial synthetic hydrochloric acid, 5% of high-temperature corrosion inhibitor, 5% of wetting agent for oil extraction, 3% of cleanup additive for fracturing, 3% of iron ion stabilizer, 2% of clay stabilizer and the balance of water.
For the above-mentioned various acid fracturing fluids, each of the components contained therein may be common in the art and may be commercially available. For example, the water may be clean water, the wetting agent for oil recovery may be ether, the cleanup additive for fracturing may be a fluorocarbon surfactant, the iron ion stabilizer may be an organic sodium salt, the clay stabilizer may be an organic salt, the corrosion inhibitor for acidification may be a quaternary ammonium salt corrosion inhibitor, and the gelling agent for acidification may be a sulfopolymer gelling agent, which is not illustrated herein.
In the acid fracturing process, in order to obtain good acid fracturing effect and make the acid fracturing process more controllable, the discharge capacity of the various acid fracturing fluids can be controlled at 6.5m3/min-7.5m3Min, e.g. 6.5m3/min、6.7m3/min、6.8m3/min、6.9m3/min、7.0m3/min、7.1m3/min、7.2m3/min、7.3m3/min、7.4m3Min, etc.
When the various acid fracturing fluids are injected into the well bore, the injection is carried out at a design pressure, and the design pressure can be obtained by the following formula for each acid fracturing fluid:
Pw=Pk-Ph+Pf
wherein, PwTo design the pressure, PkTo a breaking pressure, PhIs hydrostatic column pressure, PfThe pipelines are friction resistance and the units of the pipelines are the same.
The usage amount of the various acid fracturing fluids can be calculated according to oil layer data and Meyer software simulation, in general, for the high-temperature carbonate rock reservoir in the buried hill, in order to obtain a good acid fracturing effect and avoid excessive usage amount, the usage amount of the various acid fracturing fluids can be in the following range, and the specific usage amount of the various acid fracturing fluids is adjusted in a targeted manner according to the specific situation of a target well:
for the resistance reducing liquid, the first dosage referred to above is 200m3-1000m3For example, 200m3、300m3、400m3、500m3、600m3、700m3、800m3、900m3、1000m3Etc.;the fifth dosage is 200m3-500m3For example, 200m3、300m3、400m3、500m3Etc.; the ninth dosage is 20m3-80m3E.g. 20m3、30m3、40m3、50m3、60m3、70m3、80m3And the like.
For the crosslinking acid, the second amount referred to above is 100m3-300m3E.g. 100m3、150m3、200m3、250m3、300m3Etc.; the sixth dosage is 100m3-300m3E.g. 100m3、150m3、200m3、250m3、300m3And the like.
For the gelled acid, the third quantity referred to above is 300m3-500m3E.g. 300m3、350m3、400m3、450m3、500m3Etc.; the seventh dosage is 100m3-300m3E.g. 100m3、150m3、200m3、250m3、300m3And the like.
For diverting acids, the fourth quantity referred to above is 200m3-300m3E.g. 200m3、250m3、300m3And the like.
For the closed acid, the eighth dosage is 20m3-80m3E.g. 20m3、30m3、40m3、50m3、60m3、70m3、80m3And the like.
In actual operation, the resistance reducing liquid, the gelled acid, the cross-linking acid, the steering acid and the closed acid can be respectively added into different liquid storage tanks, each liquid storage tank is connected with a ground pipeline, valves are arranged on the ground pipelines, the five ground pipelines are converged and then connected with a high-pressure pipeline, and the injection pump is connected with the Christmas tree through the high-pressure pipeline.
The invention is further illustrated by the following specific examples:
in the following examples, the compositions of the various acid fracturing fluids used are as follows:
the resistance reducing liquid comprises the following components in percentage by mass: 0.8% of resistance reducing agent and the balance of water.
The gelled acid comprises the following components in percentage by mass: 15% of industrial synthetic hydrochloric acid, 10% of gelling agent for acidification, 3% of corrosion inhibitor, 3% of iron ion stabilizer, 3% of cleanup additive, 3% of wetting agent for oil recovery, 2% of clay stabilizer and the balance of water.
The crosslinking acid comprises the following components in percentage by mass: 20 percent of industrial synthetic hydrochloric acid, 0.4 percent of cross-linked acid liquid conditioner for acidification, 0.8 percent of cross-linked acid thickener for acidification, 5 percent of high-temperature corrosion inhibitor, 3 percent of wetting agent for oil extraction, 3 percent of cleanup additive for fracturing, 3 percent of iron ion stabilizer, 2 percent of clay stabilizer and the balance of water.
The diverting acid comprises the following components in percentage by mass: 20% of industrial synthetic hydrochloric acid, 5% of high-temperature corrosion inhibitor, 5% of self-diverting agent for acidification, 5% of wetting agent for oil recovery, 3% of cleanup additive for fracturing, 3% of iron ion stabilizer, 2% of clay stabilizer and the balance of water.
The closed acid comprises the following components in percentage by mass: 20% of industrial synthetic hydrochloric acid, 5% of high-temperature corrosion inhibitor, 5% of wetting agent for oil extraction, 3% of cleanup additive for fracturing, 3% of iron ion stabilizer, 2% of clay stabilizer and the balance of water.
Example 1
Using the object: the well comprises a Qx1 well, well sections 3991.9 m-4040 m, 29.5m/6 layers and a total span of 48.1m, wherein the layer is an Odoku Shanjia ditch group, and a reservoir is buried deeply and belongs to a high-temperature deep well.
The method provided by the embodiment of the invention is used for carrying out acid fracturing on the Qx1 well, and the related operation parameters are shown in the following table 1:
TABLE 1
Figure BDA0002359280360000081
After the acid fracturing method is implemented, the well is closed for 3 hoursThe acid reacts and then the well is opened. Tests show that Qx1 well produces no oil before acid fracturing, 22.3 tons of oil produced in the day after acid fracturing and 5.7X 10 tons of gas produced in the day4m3
Example 2
Using the object: bx1 well, well section 4630.9-4653.4m, 18m/5 layers, total span 22.5m, the layer is Ordovician; the reservoir is buried deeply and belongs to a high-temperature deep well Bx1 well, the well section is 4630.9-4653.4m, the total span is 22.5m, and the layer is an Ordovician; the reservoir is buried deeply and belongs to a high-temperature deep well.
The Bx1 wells were subjected to acid fracturing using the method provided by the embodiment of the present invention, and the related operating parameters are shown in table 2 below:
TABLE 2
Figure BDA0002359280360000082
After the acid fracturing method is implemented, the well is closed for 2 hours, and then the well is opened after the acid reaction. Tests show that the oil can not be produced before the Bx1 well is subjected to acid fracturing, the daily oil production is 21.65 tons after the acid fracturing, and the daily gas production is 5.43 multiplied by 104m3
The above description is only for facilitating the understanding of the technical solutions of the present invention by those skilled in the art, and is not intended to limit the present invention. Any modification, equivalent replacement, or improvement made within the spirit and principle of the present invention should be included in the protection scope of the present invention.

Claims (10)

1. A method of acid fracturing a carbonate reservoir, the method comprising: injecting acid fracturing fluid into the shaft to a target layer through the oil pipe and/or the oil sleeve annulus;
closing the well for setting time to finish acid fracturing;
wherein the acid fracturing fluid comprises: resistance reducing liquid, gelled acid, cross-linked acid, diverting acid and closed acid;
the step of injecting the acid fracturing fluid into the well bore comprises the following steps in sequence: injecting the resistance reducing fluid into the shaft to a target layer according to the first dosage;
continuing to inject the crosslinking acid into the wellbore to the target zone according to the second dosage;
according to a third dosage, continuously injecting the gelled acid into the shaft until the target layer is formed;
according to a fourth dosage, continuing to inject the diverting acid into the well bore to the target layer;
according to a fifth dosage, continuing to inject the resistance reducing fluid into the shaft until the target layer is reached;
continuing to inject the crosslinking acid into the wellbore to the target zone according to a sixth dosage;
according to a seventh dosage, continuing to inject the gelled acid into the well bore to the target layer;
continuing to inject the closure acid into the wellbore to the zone of interest at an eighth dosage below fracture closure pressure;
and continuing to inject the resistance reducing fluid into the well bore to the target layer according to a ninth dosage under the condition of lower than the fracture closing pressure.
2. The acid fracturing method of a carbonate reservoir according to claim 1, wherein the resistance reducing fluid comprises the following components in percentage by mass: 0.5-1% of resistance reducing agent and the balance of water.
3. The acid fracturing method of a carbonate reservoir according to claim 1, wherein the gelled acid comprises the following components in percentage by mass: 10 to 20 percent of industrial synthetic hydrochloric acid, 10 to 15 percent of gelling agent for acidification, 2 to 5 percent of corrosion inhibitor, 2 to 5 percent of iron ion stabilizer, 2 to 5 percent of cleanup additive, 2 to 5 percent of wetting agent for oil recovery, 1 to 3 percent of clay stabilizer and the balance of water.
4. The acid fracturing method of a carbonate reservoir according to claim 1, wherein the cross-linking acid comprises the following components in percentage by mass: 10 to 20 percent of industrial synthetic hydrochloric acid, 0.2 to 0.5 percent of crosslinking acid liquid conditioner for acidification, 0.5 to 1 percent of crosslinking acid thickener for acidification, 3 to 8 percent of high-temperature corrosion inhibitor, 3 to 8 percent of wetting agent for oil extraction, 2 to 5 percent of cleanup additive for fracturing, 2 to 5 percent of iron ion stabilizer, 2 to 5 percent of clay stabilizer and the balance of water.
5. The acid fracturing method of a carbonate reservoir according to claim 1, wherein the diverting acid comprises the following components in percentage by mass: 10 to 30 percent of industrial synthetic hydrochloric acid, 3 to 8 percent of high-temperature corrosion inhibitor, 3 to 8 percent of self-steering agent for acidification, 3 to 8 percent of wetting agent for oil extraction, 2 to 5 percent of cleanup additive for fracturing, 2 to 5 percent of iron ion stabilizer, 2 to 5 percent of clay stabilizer and the balance of water.
6. The acid fracturing method of a carbonate reservoir according to claim 1, wherein the closed acid comprises the following components in percentage by mass: 10 to 30 percent of industrial synthetic hydrochloric acid, 3 to 8 percent of high-temperature corrosion inhibitor, 3 to 8 percent of wetting agent for oil extraction, 2 to 5 percent of cleanup additive for fracturing, 2 to 5 percent of iron ion stabilizer, 2 to 5 percent of clay stabilizer and the balance of water.
7. The acid fracturing method of a carbonate reservoir according to claim 1, wherein the first amount is 200m for the drag reducing fluid3-1000m3The fifth dosage is 200m3-500m3The ninth dosage is 20m3-80m3
8. The acid fracturing method of a carbonate reservoir according to claim 1, wherein the second amount is 100m for the cross-linking acid3-300m3The sixth dosage is 100m3-300m3
9. The acid fracturing method of a carbonate reservoir according to claim 1, characterized in that for the gelled acid, the third purpose isThe amount is 300m3-500m3The seventh dosage is 100m3-300m3
10. The acid fracturing method of a carbonate reservoir according to claim 1, wherein for the diverting acid, the fourth amount is 200m3-300m3
For the blocking acid, the eighth amount is 20m3-80m3
CN202010017020.5A 2020-01-08 2020-01-08 Acid fracturing method for carbonate reservoir Pending CN113090241A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202010017020.5A CN113090241A (en) 2020-01-08 2020-01-08 Acid fracturing method for carbonate reservoir

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202010017020.5A CN113090241A (en) 2020-01-08 2020-01-08 Acid fracturing method for carbonate reservoir

Publications (1)

Publication Number Publication Date
CN113090241A true CN113090241A (en) 2021-07-09

Family

ID=76663357

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202010017020.5A Pending CN113090241A (en) 2020-01-08 2020-01-08 Acid fracturing method for carbonate reservoir

Country Status (1)

Country Link
CN (1) CN113090241A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN117287173A (en) * 2023-11-27 2023-12-26 中国矿业大学 Carbonate geothermal reservoir fracturing process method

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120156787A1 (en) * 2010-12-15 2012-06-21 Saudi Arabian Oil Company Laboratory Testing Procedure to Select Acid or Proppant Fracturing Stimulation Treatment for a Given Carbonate Formation
CN104989361A (en) * 2015-07-13 2015-10-21 中国石油大学(北京) Method for auxiliary horizontal well artificial fracture direction change transformation
CN105041288A (en) * 2015-07-13 2015-11-11 中国石油大学(北京) Fractural diverting acid-fracturing method for carbonate oil-gas reservoirs
CN107255027A (en) * 2017-07-13 2017-10-17 西南石油大学 A kind of carbonate reservoir is combined remodeling method
CN110439527A (en) * 2019-07-18 2019-11-12 西南石油大学 A kind of carbonate reservoir presses method from drop acid filtering

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120156787A1 (en) * 2010-12-15 2012-06-21 Saudi Arabian Oil Company Laboratory Testing Procedure to Select Acid or Proppant Fracturing Stimulation Treatment for a Given Carbonate Formation
CN104989361A (en) * 2015-07-13 2015-10-21 中国石油大学(北京) Method for auxiliary horizontal well artificial fracture direction change transformation
CN105041288A (en) * 2015-07-13 2015-11-11 中国石油大学(北京) Fractural diverting acid-fracturing method for carbonate oil-gas reservoirs
CN107255027A (en) * 2017-07-13 2017-10-17 西南石油大学 A kind of carbonate reservoir is combined remodeling method
CN110439527A (en) * 2019-07-18 2019-11-12 西南石油大学 A kind of carbonate reservoir presses method from drop acid filtering

Non-Patent Citations (7)

* Cited by examiner, † Cited by third party
Title
中国石油天然气总公司劳资局,石油工业出版社, vol. 1, 石油工业出版社, pages: 162 - 163 *
中国石油天然气总公司劳资局,石油工业出版社, 石油工业出版社 *
俞绍诚等: "《压裂酸化工艺技术》", 31 January 1998, 北京:石油工业出版社, pages: 649 - 651 *
党伟等: "多级注入酸压技术在南堡油田的应用", 《钻井液与完井液》 *
党伟等: "多级注入酸压技术在南堡油田的应用", 《钻井液与完井液》, vol. 29, no. 05, 30 September 2012 (2012-09-30), pages 74 - 76 *
杨川东: "《采气工程》", 28 February 2001, 北京:石油工业出版社, pages: 180 - 184 *
闫钰等: "大港潜山高温油气藏酸压工艺研究", 《化学工程与装备》, no. 09, 30 September 2016 (2016-09-30), pages 71 - 76 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN117287173A (en) * 2023-11-27 2023-12-26 中国矿业大学 Carbonate geothermal reservoir fracturing process method

Similar Documents

Publication Publication Date Title
CN107255027B (en) Compound modification method for carbonate rock reservoir
CN102022105B (en) Large composite acid fracturing method of fracture cave type carbonate rock reservoir
CN105089603A (en) Reservoir modifying method through forming crack network by temporary plugging turning in cracks
US9938810B2 (en) Conductivity enhancement of complex fracture networks in subterranean formations
CN110388199B (en) Large-discharge-capacity composite acid fracturing modification method for carbonate reservoir
CN106567702A (en) Method for improving complexity index of deep shale gas fracture
CN104295275A (en) Deep blockage removal and injection increase method for water injection well of medium-and-high-permeability sandstone reservoir
CN104989361A (en) Method for auxiliary horizontal well artificial fracture direction change transformation
CN105089600A (en) Temporary blocking material assisted dragged hydraulic jet reconstruction method for horizontal well
CN102587873A (en) Carbon oxide huff-n-puff, water control and oil increment method for horizontal well
CN110656920B (en) Acid fracturing method for complex fractures in carbonate reservoir
CN110005388B (en) Fracturing and yield increasing method for 3-inch semi-slim well side drilling of ultra-low permeability oil reservoir
CN104847317A (en) Method for raising recovery efficiency of super-deep low permeability heavy oil reservoir
CN108913118A (en) One kind being used for high water-cut reservoir water-control oil-increasing acidification technique method
CN110685656A (en) Fracturing and three-mining integrated construction method for low-permeability oil reservoir
CN103821486B (en) A kind of new chemical is handled up method for increasing
CN107060704A (en) Supercritical CO2It is atomized deep penetration acid fracturing method
CN111764871A (en) Natural gas hydrate reservoir direct-increasing horizontal mining method
CN113090241A (en) Acid fracturing method for carbonate reservoir
CN110318725A (en) A kind of remodeling method of geothermal reservoir
CN105756649A (en) Yield increase method for low-permeability wax-bearing oil well
CN116875296A (en) Solid acid precursor for reservoir reformation
CN103912255B (en) A kind of Oil/gas Well hydraulic oscillation fracturing technology
CN113818854B (en) Composite acid fracturing method for improving diversion capacity of ultra-deep carbonate reservoir and application thereof
RU2012114259A (en) METHOD FOR INCREASING OIL, GAS CONDENSATES AND GAS PRODUCTION FROM DEPOSITS AND ENSURING UNINTERRUPTED OPERATION OF PRODUCING AND EXPRESSIVE WELLS

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20210709