CN110003870A - A kind of pressure break degradable water dissolubility diverting agent and preparation method thereof - Google Patents

A kind of pressure break degradable water dissolubility diverting agent and preparation method thereof Download PDF

Info

Publication number
CN110003870A
CN110003870A CN201910392863.0A CN201910392863A CN110003870A CN 110003870 A CN110003870 A CN 110003870A CN 201910392863 A CN201910392863 A CN 201910392863A CN 110003870 A CN110003870 A CN 110003870A
Authority
CN
China
Prior art keywords
diverting agent
pressure break
acrylamide
bentonite
added
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
CN201910392863.0A
Other languages
Chinese (zh)
Inventor
常冬梅
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.)
Zhongke Baochen (beijing) Technology Co Ltd
Original Assignee
Zhongke Baochen (beijing) Technology 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 Zhongke Baochen (beijing) Technology Co Ltd filed Critical Zhongke Baochen (beijing) Technology Co Ltd
Priority to CN201910392863.0A priority Critical patent/CN110003870A/en
Publication of CN110003870A publication Critical patent/CN110003870A/en
Pending legal-status Critical Current

Links

Classifications

    • 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
    • C09K8/50Compositions for plastering borehole walls, i.e. compositions for temporary consolidation of borehole walls
    • C09K8/504Compositions based on water or polar solvents
    • C09K8/5045Compositions based on water or polar solvents containing inorganic compounds
    • 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
    • C09K8/50Compositions for plastering borehole walls, i.e. compositions for temporary consolidation of borehole walls
    • C09K8/504Compositions based on water or polar solvents
    • C09K8/506Compositions based on water or polar solvents containing organic compounds
    • C09K8/508Compositions based on water or polar solvents containing organic compounds macromolecular compounds
    • C09K8/5083Compositions based on water or polar solvents containing organic compounds macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • 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
    • C09K8/50Compositions for plastering borehole walls, i.e. compositions for temporary consolidation of borehole walls
    • C09K8/504Compositions based on water or polar solvents
    • C09K8/506Compositions based on water or polar solvents containing organic compounds
    • C09K8/508Compositions based on water or polar solvents containing organic compounds macromolecular compounds
    • C09K8/5086Compositions based on water or polar solvents containing organic compounds macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • 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
    • C09K8/50Compositions for plastering borehole walls, i.e. compositions for temporary consolidation of borehole walls
    • C09K8/504Compositions based on water or polar solvents
    • C09K8/506Compositions based on water or polar solvents containing organic compounds
    • C09K8/508Compositions based on water or polar solvents containing organic compounds macromolecular compounds
    • C09K8/512Compositions based on water or polar solvents containing organic compounds macromolecular compounds containing cross-linking agents
    • 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
    • C09K8/50Compositions for plastering borehole walls, i.e. compositions for temporary consolidation of borehole walls
    • C09K8/504Compositions based on water or polar solvents
    • C09K8/506Compositions based on water or polar solvents containing organic compounds
    • C09K8/508Compositions based on water or polar solvents containing organic compounds macromolecular compounds
    • C09K8/514Compositions based on water or polar solvents containing organic compounds macromolecular compounds of natural origin, e.g. polysaccharides, cellulose

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Soil Conditioners And Soil-Stabilizing Materials (AREA)

Abstract

The invention discloses a kind of pressure break degradable water dissolubility diverting agents, the diverting agent is prepared by the raw material of following mass percent: acrylamide 10~30%, acrylic acid 10~20%, bentonite 5~10%, starch 5~10%, sulfonated gilsonite 5~10%, 2- acrylamide-2-methyl propane sulfonic 5~10%, crosslinking agent account for the 0.01~0.05% of monomer mass, initiator and account for the 0.4~0.8% of monomer mass, and surplus is distilled water.Diverting agent of the invention enters in bottom crack with fracturing fluid, in carrying process and reaches in short time in crack, water swelling and toughness is fine, counterincision is sewed with good plugging action.And in the short time, due to stratum high-temperature, diverting agent can voluntarily degrade, to reach temporarily stifled effect well.And preparation method of the invention is simple, cost of material is low and comparatively safe.

Description

A kind of pressure break degradable water dissolubility diverting agent and preparation method thereof
Technical field
The invention belongs to the technical fields of material, and in particular to a kind of pressure break degradable water dissolubility diverting agent and its preparation Method.
Background technique
Petroleum plays a significant role as the efficient energy in world economy.And the average oil recovery in the whole world down to 34%, the life for extending mature oilfield reservoir is one of primary goal of energy industry.The exploration of petroleum is become more in recent years Add difficulty, this makes us, and it is necessary to improve the tar productivity of petroleum.
With the fast development of China's economy and society, the petroleum valuable source indispensable and non-renewable as one kind, In occupation of very important status.In petroleum industry and petroleum industry technology gradually development process, the scholars that go in for the study Also face the problem of some sternnesses: firstly, since Chinese population is numerous, oil demand amount is quicklyd increase, and oilfield exploitation quantity It is limited, so that supply falls short of demand;Secondly, petroleum industry technology is advanced not enough, cause the petroleum largely remained in depleted reservoir Fail full extraction to come out.It can be seen that using petroleum resources in order to more permanent, it would be desirable to accomplish scientific and reasonable Using, improve petroleum industry technology with achieve the purpose that improve production efficiency.
And oilfield exploitation dynamics increasingly increases, oily resource enters the deficient phase.Enter stage middle and later periods, oil well in oil exploitation Water content is almost up to 99% or more.Therefore, people are gradually by oil recovery target diversion to the secondary of water injection well and hyposmosis oil well Even repeatedly in exploitation.
To increase oil extraction amount, chemical temporary blocking agent is widely used in oilfield construction production.Meghan et al. was once It points out: exploitation purpose being oriented to less permeable layer or oil production can be increased to the method for high permeability zone selective shut-off.
Currently, acid, alkalinity and oil diverting agent are relatively more, water-soluble diverting agent type is few.And it is short without a kind of energy The degradable water insoluble chemical diverting agent that time blocks.
Summary of the invention
In order to solve the above technical problems, the present invention provides a kind of pressure break degradable water dissolubility diverting agents and its preparation Method.The chemical temporary blocking agent is low cost, environmental protection and the water-soluble diverting agent that can voluntarily degrade after mining.
Technical scheme is as follows:
The present invention provides a kind of pressure break degradable water dissolubility diverting agent, the diverting agent by following mass percent original Material prepares: acrylamide 10~30%, acrylic acid 10~20%, bentonite 5~10%, starch 5~10%, sulfonated gilsonite 5~10%, 2- acrylamide-2-methyl propane sulfonic 5~10%, crosslinking agent 0.1~1%, initiator 4~8%, surplus are distillation Water.
The present invention is directed to construction site demand, develops a kind of low cost, environmental protection and after mining can voluntarily degrade Water-soluble diverting agent.The diverting agent relies primarily on local environment temperature and controls itself degradability in water.When temperature is lower than drop When solving temperature, diverting agent can form stable temporary stifled band in Thief zone area;After the completion of measure, with the recovery of formation temperature, When reaching degradation temperature, diverting agent can decompose in water flooding completely and realize de-plugging.
For acrylamide and acrylic acid of the invention under the action of crosslinking agent, initiator, crosslinking generates tridimensional network, It blocks in basal crack area.As main reaction monomer, the amide groups and carboxyl contained makes diverting agent for acrylamide and acrylic acid With strong absorptive;For 2- acrylamide-2-methyl propane sulfonic as auxiliary reaction monomers, it is short that the sulfonic group contained increases diverting agent Heat-resistant salt-resistant in time;Bentonite, starch and sulfonated gilsonite as filler, increase diverting agent water absorbing properties and Brittleness, to accelerate to degrade.Bentonite, starch molecular structure on the hydroxyl group that contains, sulfonated gilsonite contains sulfonic group, hydroxyl Base, sulfonic group can form a kind of physical crosslinking with the hydrogen bond in water, to increase the water absorbing properties of diverting agent, therefore be conducive to temporarily The degradation of blocking agent.
Further, the bentonite is at least one of sodium bentonite, calcium-base bentonite.
Further, the starch is at least one of tapioca starch, cornstarch, potato starch.
Further, the crosslinking agent is polyethyleneglycol diacrylate (PEGDA), N, N '-methylene-bisacrylamide At least one of (NMBA).
Further, the initiator is potassium peroxydisulfate/anhydrous sodium sulfite, ammonium persulfate/sodium hydrogensulfite, tert-butyl One of hydrogen peroxide/sodium pyrosulfite, hydrogen peroxide/tartaric acid combination.
The present invention, to the selection and dosage of crosslinking agent and initiator, is true by a large amount of screening experiments from the selection of monomer It is fixed, therefore the degradable water dissolubility diverting agent prepared is had excellent performance.
The present invention also provides a kind of method for preparing the pressure break degradable water dissolubility diverting agent, this method includes Following steps:
(1) water and starch mixing are added in the reaction vessel, acrylic acid is then added and mixes;
(2) acrylamide, 2- acrylamide-2-methyl propane sulfonic, bentonite, sulphur are added in step (1) acquired solution Change pitch, heating stirring is uniform after ultrasonic disperse;
(3) crosslinking agent is added in step (2) acquired solution, initiator carries out polymerization reaction;
(4) cooling is stood, drying is after polymeric shear is granulated to get the diverting agent.
Further, in step (1), the sodium hydroxide solution that mass percent is 20~30% is added, adjusts solution PH value is 5~6.
Further, in step (2), in the case where frequency is 30-50Hz, ultrasonic disperse handles 10~15min.So that solution is mixed It closes more uniform.
Further, in step (3), the temperature of polymerization reaction is 45~55 DEG C, and the time is 20~30min.
The invention has the benefit that diverting agent of the invention enters in bottom crack with fracturing fluid, in carrying process And reach in short time in crack, water swelling and toughness is fine, counterincision is sewed with good plugging action;And in the short time, Due to stratum high-temperature, diverting agent can voluntarily degrade, to reach temporarily stifled effect well.And preparation method of the invention is simple, Cost of material is low and comparatively safe.
Detailed description of the invention
Fig. 1 is the influence of the type and dosage of crosslinking agent of the present invention to diverting agent water absorbent rate;
Fig. 2 is the influence of the type and dosage of crosslinking agent of the present invention to diverting agent degradation time;
Fig. 3 is that the present invention schemes that the SEM of the diverting agent of sulfonated gilsonite is not added;
Fig. 4 is the present invention in the SEM figure that the diverting agent of sulfonated gilsonite is added;
Fig. 5 is the infrared spectrogram of diverting agent calcium-base bentonite and other components of the present invention;
A: calcium-base bentonite;B: the diverting agent containing calcium-base bentonite;C: the diverting agent without calcium-base bentonite;
Fig. 6 is pressue-graph of the diverting agent of the present invention in reservoir core plugging.
Specific embodiment
The present invention is carried out below with reference to embodiment and attached drawing explanation is explained in detail.
Embodiment 1
A kind of pressure break degradable water dissolubility diverting agent includes the raw material of following mass percent: acrylamide 10%, third Olefin(e) acid 10%, sodium bentonite 5%, tapioca starch 5%, sulfonated gilsonite 5%, 2- acrylamide-2-methyl propane sulfonic 10%, poly- second Omega-diol diacrylate 0.1%, potassium peroxydisulfate 2.2%, anhydrous sodium sulfite 1.8%, surplus are distilled water.
The preparation method of pressure break degradable water dissolubility diverting agent the following steps are included:
(1) water and tapioca starch mixing are added in the reaction vessel, the rear acrylic acid that is added mixes, and mass percent is then added PH value for 20% sodium hydroxide solution adjusting solution is 5;
(2) acrylamide, 2- acrylamide-2-methyl propane sulfonic, Na-bentonite are added in step (1) acquired solution Soil, sulfonated gilsonite, in the case where frequency is 50Hz, ultrasonic disperse handles 10min, and 45 DEG C of heating water baths stir evenly;
(3) the addition polyethyleneglycol diacrylate, potassium peroxydisulfate, anhydrous sodium sulfite in step (2) acquired solution, 45 Polymerization reaction 30min at DEG C;
(4) cooling is stood, drying to constant weight at 50 DEG C to get the diverting agent after polymeric shear is granulated.
Embodiment 2
A kind of pressure break degradable water dissolubility diverting agent includes the raw material of following mass percent: acrylamide 30%, third Olefin(e) acid 20%, calcium-base bentonite 10%, cornstarch 10%, sulfonated gilsonite 10%, 2- acrylamide-2-methyl propane sulfonic 5%, N, N '-methylene-bisacrylamide 1%, ammonium persulfate 3.5%, sodium hydrogensulfite 2.5%, surplus are distilled water.
The preparation method of pressure break degradable water dissolubility diverting agent the following steps are included:
(1) water and cornstarch mixing are added in the reaction vessel, the rear acrylic acid that is added mixes, and quality percentage is then added Number is 6 for the pH value of 30% sodium hydroxide solution adjusting solution;
(2) acrylamide, 2- acrylamide-2-methyl propane sulfonic, calcium base swelling are added in step (1) acquired solution Soil, sulfonated gilsonite, in the case where frequency is 30Hz, ultrasonic disperse handles 15min, and 55 DEG C of heating water baths stir evenly;
(3) it is added N in step (2) acquired solution, N '-methylene-bisacrylamide, ammonium persulfate, sodium hydrogensulfite, Polymerization reaction 20min at 55 DEG C;
(4) cooling is stood, drying to constant weight at 50 DEG C to get the diverting agent after polymeric shear is granulated.
Embodiment 3
A kind of pressure break degradable water dissolubility diverting agent includes the raw material of following mass percent: acrylamide 20%, third Olefin(e) acid 15%, sodium bentonite 5%, potato starch 10%, sulfonated gilsonite 10%, 2- acrylamide-2-methyl propane sulfonic 8%, polyethyleneglycol diacrylate 0.2%, N, N '-methylene-bisacrylamide 0.3%, hydrogen peroxide 2.8%, tartaric acid 2.2%, surplus is distilled water.
The preparation method of pressure break degradable water dissolubility diverting agent the following steps are included:
(1) water and potato starch mixing are added in the reaction vessel, the rear acrylic acid that is added mixes, and quality hundred is then added The pH value that the sodium hydroxide solution that score is 20% adjusts solution is 6;
(2) acrylamide, 2- acrylamide-2-methyl propane sulfonic, Na-bentonite are added in step (1) acquired solution Soil, sulfonated gilsonite, in the case where frequency is 40Hz, ultrasonic disperse handles 12min, and 50 DEG C of heating water baths stir evenly;
(3) polyethyleneglycol diacrylate, N,N methylene bis acrylamide, mistake are added in step (2) acquired solution Hydrogen oxide, tartaric acid, polymerization reaction 25min at 50 DEG C;
(4) cooling is stood, drying to constant weight at 55 DEG C to get the diverting agent after polymeric shear is granulated.
Embodiment 4
A kind of pressure break degradable water dissolubility diverting agent includes the raw material of following mass percent: acrylamide 25%, third Olefin(e) acid 15%, sodium bentonite 5%, calcium-base bentonite 3%, cornstarch 8%, sulfonated gilsonite 8%, 2- acrylamide -2- first Base propane sulfonic acid 8%, polyethyleneglycol diacrylate 0.8%, potassium peroxydisulfate 4.5%, anhydrous sodium sulfite 3.5%, surplus are to steam Distilled water.
The preparation method of pressure break degradable water dissolubility diverting agent the following steps are included:
(1) water and cornstarch mixing are added in the reaction vessel, the rear acrylic acid that is added mixes, and quality percentage is then added Number is 6 for the pH value of 30% sodium hydroxide solution adjusting solution;
(2) acrylamide, 2- acrylamide-2-methyl propane sulfonic, Na-bentonite are added in step (1) acquired solution Soil, calcium-base bentonite, sulfonated gilsonite, in the case where frequency is 50Hz, ultrasonic disperse handles 10min, and 50 DEG C of heating water baths stir evenly;
(3) the addition polyethyleneglycol diacrylate, potassium peroxydisulfate, anhydrous sodium sulfite in step (2) acquired solution, 50 Polymerization reaction 25min at DEG C;
(4) cooling is stood, drying to constant weight at 55 DEG C to get the diverting agent after polymeric shear is granulated.
Comparative example 1
A kind of pressure break degradable water dissolubility diverting agent includes the raw material of following mass percent: acrylamide 25%, third Olefin(e) acid 15%, sodium bentonite 5%, calcium-base bentonite 3%, cornstarch 8%, sulfonated gilsonite 8%, polyethylene glycol diacrylate Ester 0.8%, potassium peroxydisulfate 4.5%, anhydrous sodium sulfite 3.5%, surplus are distilled water.
The preparation method of pressure break degradable water dissolubility diverting agent the following steps are included:
(1) water and cornstarch mixing are added in the reaction vessel, the rear acrylic acid that is added mixes, and then mass percent is The pH value that 30% sodium hydroxide solution adjusts solution is 6;
(2) acrylamide, sodium bentonite, calcium-base bentonite, sulfonated gilsonite are added in step (1) acquired solution, Frequency is that ultrasonic disperse handles 10min under 50Hz, and 50 DEG C of heating water baths stir evenly;
(3) polyethyleneglycol diacrylate, potassium peroxydisulfate, anhydrous sodium sulfite are added in step (2) acquired solution, Polymerization reaction 25min at 50 DEG C;
(4) cooling is stood, drying to constant weight at 55 DEG C to get the diverting agent after polymeric shear is granulated.
Comparative example 2
A kind of pressure break degradable water dissolubility diverting agent includes the raw material of following mass percent: acrylamide 25%, third Olefin(e) acid 15%, sodium bentonite 5%, calcium-base bentonite 3%, sulfonated gilsonite 16%, 2- acrylamide-2-methyl propane sulfonic 8%, Polyethyleneglycol diacrylate 0.8%, potassium peroxydisulfate 4.5%, anhydrous sodium sulfite 3.5%, surplus are distilled water.
The preparation method of pressure break degradable water dissolubility diverting agent the following steps are included:
(1) water and acrylic acid are added in the reaction vessel, the sodium hydroxide solution that mass percent is 30% is then added The pH value for adjusting solution is 6;
(2) acrylamide, 2- acrylamide-2-methyl propane sulfonic, Na-bentonite are added in step (1) acquired solution Soil, calcium-base bentonite, sulfonated gilsonite, in the case where frequency is 50Hz, ultrasonic disperse handles 10min, and 50 DEG C of heating water baths stir evenly;
(3) polyethyleneglycol diacrylate, potassium peroxydisulfate, anhydrous sodium sulfite are added in step (2) acquired solution, Polymerization reaction 25min at 50 DEG C;
(4) cooling is stood, drying to constant weight at 55 DEG C to get the diverting agent after polymeric shear is granulated.
Comparative example 3
A kind of pressure break degradable water dissolubility diverting agent includes the raw material of following mass percent: acrylamide 25%, third Olefin(e) acid 15%, sodium bentonite 5%, calcium-base bentonite 3%, cornstarch 16%, 2- acrylamide-2-methyl propane sulfonic 8%, Polyethyleneglycol diacrylate 0.8%, potassium peroxydisulfate 4.5%, anhydrous sodium sulfite 3.5%, surplus are distilled water.
The preparation method of pressure break degradable water dissolubility diverting agent the following steps are included:
(1) water and cornstarch mixing are added in the reaction vessel, acrylic acid is then added and mass percent is 30% Sodium hydroxide solution, sodium hydroxide solution be used to adjust solution pH value be 6;
(2) acrylamide, 2- acrylamide-2-methyl propane sulfonic, Na-bentonite are added in step (1) acquired solution Soil, calcium-base bentonite, in the case where frequency is 50Hz, ultrasonic disperse handles 10min, and 50 DEG C of heating water baths stir evenly;
(3) polyethyleneglycol diacrylate, potassium peroxydisulfate, anhydrous sodium sulfite are added in step (2) acquired solution, Polymerization reaction 25min at 50 DEG C;
(4) cooling is stood, drying to constant weight at 55 DEG C to get the diverting agent after polymeric shear is granulated.
Comparative example 4
A kind of pressure break degradable water dissolubility diverting agent includes the raw material of following mass percent: acrylamide 25%, third Olefin(e) acid 15%, sodium bentonite 13%, calcium-base bentonite 11%, 2- acrylamide-2-methyl propane sulfonic 8%, polyethylene glycol two Acrylate 0.8%, potassium peroxydisulfate 4.5%, anhydrous sodium sulfite 3.5%, surplus are distilled water.
The preparation method of pressure break degradable water dissolubility diverting agent the following steps are included:
(1) water and acrylic acid are added in reaction vessel, the sodium hydroxide solution tune that mass percent is 30% is then added The pH value for saving solution is 6;
(2) acrylamide, 2- acrylamide-2-methyl propane sulfonic, Na-bentonite are added in step (1) acquired solution Soil, calcium-base bentonite, in the case where frequency is 50Hz, ultrasonic disperse handles 10min, and 50 DEG C of heating water baths stir evenly;
(3) the addition polyethyleneglycol diacrylate, potassium peroxydisulfate, anhydrous sodium sulfite in step (2) acquired solution, 50 Polymerization reaction 25min at DEG C;
(4) cooling is stood, drying to constant weight at 55 DEG C to get the diverting agent after polymeric shear is granulated.
Effect example
With TA company, U.S. Q50 thermogravimetric analyzer, 6100 type drill core permeability rate tester of Chandler company, the U.S., Britain Stable Micro System company's T AXTplus Texture instrument, Japan's Shimadzu JSM-6610 scanning electron microscope, German Brooker The laboratory apparatus such as Vector22 type Fourier Transform Infrared Spectrometer test diverting agent performance, test result such as 1 institute of table Show:
The performance characterization test result of diverting agent obtained by 1 embodiment of the present invention of table
As shown in table 1, the corresponding diverting agent of Examples 1 to 4 lacks in the raw material of comparative example 1 compared to comparative example 1~4 2- acrylamide-2-methyl propane sulfonic lacks starch in the raw material of comparative example 2, lacks sulfonated gilsonite in the raw material of comparative example 3, Lack starch and sulfonated gilsonite in the raw material of comparative example 4.The water absorbent rate of diverting agent of the present invention illustrates to inhale all at 120 times or more It is aqueous can all preferably;Degradation time meets temporarily stifled requirement all within 20h simultaneously;Diverting agent intensity also complies with life after water suction It produces and requires;Thermogravimetric analysis is obtained just to be started to be broken in 320 DEG C or more main chains, shows that diverting agent has good heat resistance;Temporarily Blocking agent is attained by 98% or more to the sealing ratiod of core, and maximum breakthrough pressure gradient is between 21.5~25.5MPa/m, table Bright diverting agent has good sealing characteristics.Therefore, the water imbibition, degradability, intensity of diverting agent prepared by the present invention and heat-resisting Property etc. all meets production requirement.
When control other conditions are constant, when only changing type of crosslinking agent and dosage, diverting agent water absorbent rate and degradation time As shown in Figure 1, 2.As shown in Figure 1, 2, addition PEGDA ratio NMBA diverting agent water absorbent rate is high and degradation time is short.Mainly because For the high polymer prepared by PEGDA, the longer easy adjusting of strand, crosslinking is uniformly;NMBA strand is shorter, with reaction into Row, reactivity are gradually reduced, easily formation linear polymer.
As shown in Figure 3,4, the SEM of diverting agent of the invention after sulfonated gilsonite is added, after diverting agent water suction freeze-drying Figure.As can be seen from the figure plus after the water suction of the diverting agent of sulfonated gilsonite space lattice is intensive, but overall structure compares consolidation, and table Face is more smooth, without obvious fold, space lattice more crypto set after the diverting agent water suction of sulfonated gilsonite is added, and be in loose lamella Shape, gully shape, therefore it is more advantageous to diverting agent water suction and degradation.
As shown in figure 5, curve a calcium-base bentonite 3625cm-1For the stretching vibration absworption peak of Al-O-H, 3425cm-1For layer Between water-OH stretching vibration absworption peak, acrylic acid-OH absorption band is in 3425,3625cm in c-1Place contains swelling without absorption, curve b The diverting agent 3431cm of soil-1Merge for calcium-base bentonite Al-O-H with the stretching vibration absworption peak of acrylic acid-OH, but 3625cm-1 Obviously weaken at peak, it may be possible to which hydroxyl takes part in reaction in bentonite, weakens hydrogen bond action, mobile to long wave direction, it is also possible to It is that dihydroxypropyl masks bentonite hydroxyl, correlation curve c illustrates that bentonitic participation has not significant impact product structure. Curve a, 1039cm-1It is nearby the asymmetric stretching vibration absorption peak of bentonite Si-O-Si, intensity is small, and calcic base is not swollen by curve c Profit is native, and absorption peak is obviously influenced by bentonite in curve b, appears in 1050cm-1Place.
Sealing agent of the invention tests the pressure of core when blocking core.It will be appreciated from fig. 6 that working as trickle When flowing out 1.5 times of PV (pore-body accumulated amount), pressure reaches maximum value at this time, with the increase of PV volume, the main duct of core It is dead by blocking.When efflux is up to 4 times of PV volumes, pressure starts to reduce, and illustrates that diverting agent has been introduced into entire core, and by It blocks.When reaching 7 times of PV volumes, pressure drop, diverting agent starts to degrade at this time, and when up to 14 times of PV volumes, pressure becomes In constant, diverting agent degradation is complete.
The foregoing is merely illustrative of the preferred embodiments of the present invention, is not intended to limit the invention, all in essence of the invention Made any modification, equivalent replacement and simple modifications etc., should all be included in the protection scope of the present invention in content.

Claims (9)

1. a kind of pressure break degradable water dissolubility diverting agent, which is characterized in that the diverting agent by following mass percent raw material It prepares: acrylamide 10~30%, acrylic acid 10~20%, bentonite 5~10%, starch 5~10%, sulfonated gilsonite 5 ~10%, 2- acrylamide-2-methyl propane sulfonic 5~10%, crosslinking agent account for the 0.01~0.05% of monomer mass, initiator and account for The 0.4~0.8% of monomer mass, surplus are distilled water.
2. pressure break according to claim 1 degradable water dissolubility diverting agent, which is characterized in that the bentonite is sodium base At least one of bentonite, calcium-base bentonite.
3. pressure break according to claim 1 degradable water dissolubility diverting agent, which is characterized in that the starch is cassava At least one of powder, cornstarch, potato starch.
4. pressure break according to claim 1 degradable water dissolubility diverting agent, which is characterized in that the crosslinking agent is poly- second Omega-diol diacrylate, N, at least one of N '-methylene-bisacrylamide.
5. pressure break according to claim 1 degradable water dissolubility diverting agent, which is characterized in that the initiator is over cure Sour potassium/anhydrous sodium sulfite, ammonium persulfate/sodium hydrogensulfite, tert-butyl hydroperoxide/sodium pyrosulfite, hydrogen peroxide/winestone One of acid combination.
6. a kind of method for preparing pressure break degradable water dissolubility diverting agent described in claim 1, which is characterized in that this method The following steps are included:
(1) water and starch mixing are added in the reaction vessel, acrylic acid is then added and mixes;
(2) acrylamide, 2- acrylamide-2-methyl propane sulfonic, bentonite, sulfonation drip are added in step (1) acquired solution Blueness, heating stirring is uniform after ultrasonic disperse;
(3) crosslinking agent is added in step (2) acquired solution, initiator carries out polymerization reaction;
(4) cooling is stood, drying is after polymeric shear is granulated to get the diverting agent.
7. the pressure break according to claim 6 preparation method of degradable water dissolubility diverting agent, which is characterized in that step (1) in, the sodium hydroxide solution that mass percent is 20~30% is added, the pH value for adjusting solution is 5~6.
8. the pressure break according to claim 6 preparation method of degradable water dissolubility diverting agent, which is characterized in that step (2) in, in the case where frequency is 30~50Hz, ultrasonic disperse handles 10~15min.
9. the pressure break according to claim 6 preparation method of degradable water dissolubility diverting agent, which is characterized in that step (3) in, the temperature of polymerization reaction is 45~55 DEG C, and the time is 20~30min.
CN201910392863.0A 2019-05-13 2019-05-13 A kind of pressure break degradable water dissolubility diverting agent and preparation method thereof Pending CN110003870A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910392863.0A CN110003870A (en) 2019-05-13 2019-05-13 A kind of pressure break degradable water dissolubility diverting agent and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910392863.0A CN110003870A (en) 2019-05-13 2019-05-13 A kind of pressure break degradable water dissolubility diverting agent and preparation method thereof

Publications (1)

Publication Number Publication Date
CN110003870A true CN110003870A (en) 2019-07-12

Family

ID=67176629

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201910392863.0A Pending CN110003870A (en) 2019-05-13 2019-05-13 A kind of pressure break degradable water dissolubility diverting agent and preparation method thereof

Country Status (1)

Country Link
CN (1) CN110003870A (en)

Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110283578A (en) * 2019-07-18 2019-09-27 西南石油大学 A kind of water-soluble diverting agent and preparation method thereof suitable for secondary fracturing
CN110669484A (en) * 2019-09-17 2020-01-10 大港油田集团有限责任公司 Degradable temporary plugging agent for well repair and preparation method thereof
CN111303849A (en) * 2020-04-02 2020-06-19 中国石油大学(华东) Temporary plugging agent, preparation method thereof and high-temperature reservoir temporary plugging diversion fracturing method
CN111320974A (en) * 2020-04-20 2020-06-23 大庆市新万通科技开发有限公司 Acidizing temporary plugging agent and preparation method and application thereof
CN111518532A (en) * 2020-06-05 2020-08-11 西安奥德石油工程技术有限责任公司 Staged fracturing temporary plugging agent for horizontal well and preparation method thereof
CN111592871A (en) * 2020-06-05 2020-08-28 西安奥德石油工程技术有限责任公司 Shale oil shale gas fracturing temporary plugging agent and preparation method thereof
CN111621274A (en) * 2020-04-30 2020-09-04 中国石油大学(华东) Controllable degradable water swelling type fracturing temporary plugging agent, preparation method and application thereof
CN111662697A (en) * 2020-06-03 2020-09-15 中国石油天然气集团有限公司 Self-degradation temporary plugging agent and preparation method thereof
CN111876140A (en) * 2020-06-08 2020-11-03 长江大学 Dual-response self-degradation temporary plugging agent and preparation method thereof
CN111965065A (en) * 2020-08-28 2020-11-20 上海浦景化工技术股份有限公司 Method for testing and evaluating degradation performance of organic temporary plugging agent for oil and gas field
CN112940699A (en) * 2021-02-18 2021-06-11 维欧(天津)能源技术服务股份有限公司 Preparation method of composite temporary plugging agent for temporary plugging diversion fracturing
CN113736027A (en) * 2021-09-26 2021-12-03 兰州理工大学 Polymer gel temporary plugging agent, multistage structure gel temporary plugging agent obtained by using same and preparation method of multistage structure gel temporary plugging agent
CN114836184A (en) * 2022-04-26 2022-08-02 中海油(天津)油田化工有限公司 Degradable temporary plugging agent for well repair of offshore large-leakage oil-water well and use method thereof
CN116536785A (en) * 2023-06-07 2023-08-04 东营施普瑞石油工程技术有限公司 Fiber for fracturing and preparation method thereof
CN117264620A (en) * 2023-09-19 2023-12-22 西安石油大学 Oilfield fracturing high-temperature-resistant degradable temporary plugging agent and preparation method thereof
CN117917443A (en) * 2023-11-14 2024-04-23 哈尔滨工业大学 Starch-based cement-based material internal curing agent with high water absorption and high salt tolerance, and preparation method and application thereof
CN118146775A (en) * 2024-05-09 2024-06-07 西南石油大学 Double-crosslinking thermal phase-change gel temporary plugging agent and application thereof

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1869147A (en) * 2005-05-25 2006-11-29 中国石油天然气股份有限公司 Hydrolyzable high-elasticity temporary plugging agent for workover fluid
CN101586023A (en) * 2009-07-08 2009-11-25 中国石油大学(华东) High-strength pre-crosslinked gel sealing agent for drilling well and preparation method thereof
CN101724383A (en) * 2008-10-15 2010-06-09 中国石油天然气股份有限公司 Drilling fluid plugging agent while drilling
CN103361040A (en) * 2013-08-06 2013-10-23 东北石油大学 Temporary plugging agent and preparation method thereof
CN103409121A (en) * 2013-07-23 2013-11-27 中国石油天然气股份有限公司 Water-soluble temporary plugging diversion agent for fracturing and preparation method thereof
CN104087275A (en) * 2014-07-14 2014-10-08 中国石油大学(华东) High-temperature-resistant and high-salt-resistant fine gel particle as profile control agent as well as preparation method and application of fine gel particle
CN104861953A (en) * 2015-04-17 2015-08-26 四川捷贝通能源科技有限公司 Oil field fracture temporary plugging agent and preparation method thereof
CN106634903A (en) * 2016-10-12 2017-05-10 中国石油大学(华东) Interpenetrating polymer network jelly and preparation method and application thereof

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1869147A (en) * 2005-05-25 2006-11-29 中国石油天然气股份有限公司 Hydrolyzable high-elasticity temporary plugging agent for workover fluid
CN101724383A (en) * 2008-10-15 2010-06-09 中国石油天然气股份有限公司 Drilling fluid plugging agent while drilling
CN101586023A (en) * 2009-07-08 2009-11-25 中国石油大学(华东) High-strength pre-crosslinked gel sealing agent for drilling well and preparation method thereof
CN103409121A (en) * 2013-07-23 2013-11-27 中国石油天然气股份有限公司 Water-soluble temporary plugging diversion agent for fracturing and preparation method thereof
CN103361040A (en) * 2013-08-06 2013-10-23 东北石油大学 Temporary plugging agent and preparation method thereof
CN104087275A (en) * 2014-07-14 2014-10-08 中国石油大学(华东) High-temperature-resistant and high-salt-resistant fine gel particle as profile control agent as well as preparation method and application of fine gel particle
CN104861953A (en) * 2015-04-17 2015-08-26 四川捷贝通能源科技有限公司 Oil field fracture temporary plugging agent and preparation method thereof
CN106634903A (en) * 2016-10-12 2017-05-10 中国石油大学(华东) Interpenetrating polymer network jelly and preparation method and application thereof

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
常冬梅: "储层改造可降解暂堵剂的制备及表征", 《精细化工》 *
常冬梅: "水膨性暂堵剂的制备及表征", 《应用化工》 *

Cited By (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110283578B (en) * 2019-07-18 2021-10-01 西南石油大学 Water-soluble temporary plugging agent suitable for secondary fracturing and preparation method thereof
CN110283578A (en) * 2019-07-18 2019-09-27 西南石油大学 A kind of water-soluble diverting agent and preparation method thereof suitable for secondary fracturing
CN110669484A (en) * 2019-09-17 2020-01-10 大港油田集团有限责任公司 Degradable temporary plugging agent for well repair and preparation method thereof
CN111303849A (en) * 2020-04-02 2020-06-19 中国石油大学(华东) Temporary plugging agent, preparation method thereof and high-temperature reservoir temporary plugging diversion fracturing method
CN111303849B (en) * 2020-04-02 2021-05-28 中国石油大学(华东) Temporary plugging agent, preparation method thereof and high-temperature reservoir temporary plugging diversion fracturing method
CN111320974B (en) * 2020-04-20 2021-03-23 大庆市新万通科技开发有限公司 Acidizing temporary plugging agent and preparation method and application thereof
CN111320974A (en) * 2020-04-20 2020-06-23 大庆市新万通科技开发有限公司 Acidizing temporary plugging agent and preparation method and application thereof
CN111621274B (en) * 2020-04-30 2022-06-07 中国石油大学(华东) Controllable degradable water swelling type fracturing temporary plugging agent, preparation method and application thereof
CN111621274A (en) * 2020-04-30 2020-09-04 中国石油大学(华东) Controllable degradable water swelling type fracturing temporary plugging agent, preparation method and application thereof
CN111662697A (en) * 2020-06-03 2020-09-15 中国石油天然气集团有限公司 Self-degradation temporary plugging agent and preparation method thereof
CN111518532A (en) * 2020-06-05 2020-08-11 西安奥德石油工程技术有限责任公司 Staged fracturing temporary plugging agent for horizontal well and preparation method thereof
CN111592871A (en) * 2020-06-05 2020-08-28 西安奥德石油工程技术有限责任公司 Shale oil shale gas fracturing temporary plugging agent and preparation method thereof
CN111876140A (en) * 2020-06-08 2020-11-03 长江大学 Dual-response self-degradation temporary plugging agent and preparation method thereof
US11959015B2 (en) * 2020-06-08 2024-04-16 Yangtze University Double-response self-degradable temporary plugging agent and preparation method thereof
US20210380865A1 (en) * 2020-06-08 2021-12-09 Yangtze University Double-response self-degradable temporary plugging agent and preparation method thereof
CN111876140B (en) * 2020-06-08 2022-05-27 长江大学 Dual-response self-degradation temporary plugging agent and preparation method thereof
CN111965065A (en) * 2020-08-28 2020-11-20 上海浦景化工技术股份有限公司 Method for testing and evaluating degradation performance of organic temporary plugging agent for oil and gas field
CN112940699A (en) * 2021-02-18 2021-06-11 维欧(天津)能源技术服务股份有限公司 Preparation method of composite temporary plugging agent for temporary plugging diversion fracturing
CN113736027A (en) * 2021-09-26 2021-12-03 兰州理工大学 Polymer gel temporary plugging agent, multistage structure gel temporary plugging agent obtained by using same and preparation method of multistage structure gel temporary plugging agent
CN114836184A (en) * 2022-04-26 2022-08-02 中海油(天津)油田化工有限公司 Degradable temporary plugging agent for well repair of offshore large-leakage oil-water well and use method thereof
CN114836184B (en) * 2022-04-26 2024-04-12 中海油(天津)油田化工有限公司 Degradable temporary plugging agent for offshore large-leakage oil-water well workover and use method thereof
CN116536785A (en) * 2023-06-07 2023-08-04 东营施普瑞石油工程技术有限公司 Fiber for fracturing and preparation method thereof
CN116536785B (en) * 2023-06-07 2024-05-24 东营施普瑞石油工程技术有限公司 Fiber for fracturing and preparation method thereof
CN117264620A (en) * 2023-09-19 2023-12-22 西安石油大学 Oilfield fracturing high-temperature-resistant degradable temporary plugging agent and preparation method thereof
CN117917443A (en) * 2023-11-14 2024-04-23 哈尔滨工业大学 Starch-based cement-based material internal curing agent with high water absorption and high salt tolerance, and preparation method and application thereof
CN118146775A (en) * 2024-05-09 2024-06-07 西南石油大学 Double-crosslinking thermal phase-change gel temporary plugging agent and application thereof

Similar Documents

Publication Publication Date Title
CN110003870A (en) A kind of pressure break degradable water dissolubility diverting agent and preparation method thereof
CN111621274B (en) Controllable degradable water swelling type fracturing temporary plugging agent, preparation method and application thereof
CN107337762A (en) A kind of hydrophobic association cross-linked polymer microsphere, preparation method and application
CN105646777A (en) Hydrophobic associated polymer and preparation method thereof
CN102433107B (en) Low-molecular-weight polymer type filtrate loss reducer for drilling fluid and preparation method for same
CN104650828B (en) Reverse wetting agent and preparation method thereof and container horizon protective agent composition and for the drilling fluid of hyposmosis ultra-low permeability reservoir and application
CN102952533B (en) Composite cross-linked polymer weak gel oil displacement agent and preparation method thereof
CN103409130A (en) Multi-component acid pressure temporary plugging additive and preparation method thereof
CN103320112B (en) A kind of anti-shearing dendritic polymers oil-displacing agent and synthetic method thereof
CN109705834A (en) A kind of composition, the temperature-resistant anti-salt fracturing fluid thickener for utilizing the composition preparation and preparation method thereof
CN109385259A (en) A kind of AM-AMPS-NVP terpolymer-PR heatproof profile control agent and the preparation method and application thereof
CN113185630B (en) Biodegradable salt-tolerant thickening system and preparation method and application thereof
CN112409611A (en) Mussel bionic gel composition, self-repairing gel and plugging agent as well as preparation method and application of mussel bionic gel composition and self-repairing gel and plugging agent
CN110172127A (en) Nano-cellulose base sealing agent and preparation method thereof
CN105802598B (en) Modified alkali lignin plural gel blocking agent of a kind of polyacrylonitrile sodium salt and preparation method thereof
CN110483684A (en) A kind of gel particle and preparation method thereof for prevention and treatment has channeling in continuity carbon dioxide injection Drainage process
CN112851856A (en) Salt-tolerant polymer microsphere plugging agent and preparation method thereof
CN111139046A (en) Polymer gel composite plugging agent and preparation method thereof
CN113549438A (en) Water plugging agent and preparation method and application thereof
CN102559156B (en) High temperature high salinity fluid loss agent for drilling fluid and preparation method thereof
CN106046277B (en) The preparation method of reactive emulsion Gelling Water shutoff Agent
CN112778990A (en) Sewage mixing temporary plugging agent for oilfield water injection well and preparation method thereof
CN110283276A (en) A kind of oil well polyacrylamide and preparation method thereof
CN116410713A (en) Cross-linking time controllable plugging agent based on low molecular weight polyacrylamide and preparation method thereof
CN110218278A (en) A kind of oil well polyacrylamide and preparation method thereof

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: 20190712