CN101805601B - Break-free fracturing fluid - Google Patents

Break-free fracturing fluid Download PDF

Info

Publication number
CN101805601B
CN101805601B CN 201010157881 CN201010157881A CN101805601B CN 101805601 B CN101805601 B CN 101805601B CN 201010157881 CN201010157881 CN 201010157881 CN 201010157881 A CN201010157881 A CN 201010157881A CN 101805601 B CN101805601 B CN 101805601B
Authority
CN
China
Prior art keywords
parts
break
fracturing fluid
quaternary ammonium
ammonium salt
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.)
Active
Application number
CN 201010157881
Other languages
Chinese (zh)
Other versions
CN101805601A (en
Inventor
吴建平
吴琼
奈世杰
尚岩
陈刚
智勤功
谢金川
王登庆
周承诗
高雪峰
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.)
China Petroleum and Chemical Corp
Oil Production Technology Research Institute of Sinopec Shengli Oilfield Co
Original Assignee
China Petroleum and Chemical Corp
Oil Production Technology Research Institute of Sinopec Shengli Oilfield Co
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 China Petroleum and Chemical Corp, Oil Production Technology Research Institute of Sinopec Shengli Oilfield Co filed Critical China Petroleum and Chemical Corp
Priority to CN 201010157881 priority Critical patent/CN101805601B/en
Publication of CN101805601A publication Critical patent/CN101805601A/en
Application granted granted Critical
Publication of CN101805601B publication Critical patent/CN101805601B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)

Abstract

The invention discloses break-free fracturing fluid, which comprises the following components in part by weight: 1 to 3 parts of long carbon chain fatty acid salt, 2 to 8 parts of organosilicon quaternary ammonium salt monomer, 1 to 5 parts of anionic surfactant and halide, and the balance of water. The method for preparing the break-free fracturing fluid comprises the following steps: mix the 1 to 3 parts of long carbon chain fatty acid salt, 2 to 8 parts of organosilicon quaternary ammonium salt monomer and 1 to 5 parts of anionic surfactant and halide by adding the balance of water at normal temperature; and stirring and reacting for 60 to 100 minutes at the rotating speed of 500 to 1,000 revolutions per minute. The break-free fracturing fluid has the characteristics that the break-free fracturing fluid has low molecular weight, no polymer, no residue, and no breaker, can be automatically dissolved under the action of formation oil and formation water, reduces the viscosity to below 5mPa.s, does not causes loss of the core permeability, avoids secondary pollution on the stratum, can realize total flowback, and can be used at the temperature of 150 DEG C. The break-free fracturing fluid can be widely applied to oil field production technology.

Description

Break-free fracturing fluid
One, technical field
The present invention relates to oil production underground fracture operation entry well fluid, relate in particular to a kind of break-free fracturing fluid.
Two, background technology
Present fracture in oil and water wells operation working fluid; The polymer class fracturing liquid systems that adopt more; For the smooth implementation of oil well production increasing fracturing technique contributes, but exist following shortcoming or deficiency simultaneously: 1. polymkeric substance fracturing fluid residue amount is big, and is higher to the stratum permeability loss; 2. broken glue difficulty, the row of returning leads low, and fracturing liquid is prone to the stratum is produced the secondary injury; 3. the loss of pressure break fluid viscosity is big under the high temperature.According to statistics, the of the fracturing fluid row of returning of polymkeric substance such as guanidine glue leads and has only 35%-45%; 4. use temperature is low.
Three, summary of the invention
The purpose of this invention is to provide a kind of fracturing liquid of exempting from brokenly glue; The employing low-molecular weight compound is formed, and no polymkeric substance, no residue do not have injury to the stratum; Under the effect of local water or crude oil; Viscosity drops to below the 5mPa.s automatically, can realize all rows of returning, the shortcoming or the deficiency that overcome effectively or avoid existing in the above-mentioned prior art.
Break-free fracturing fluid of the present invention, its component and proportioning are following, and said proportioning is a weight part:
Long chain fatty acid salt 1-3 organosilicon quaternary ammonium salt monomer 2-8
AS 1-5 halogenide 1-5 surplus is a water,
Its compound method is: at normal temperatures; With the hard soap of 2-3 part, the organosilicon quaternary ammonium salt monomer of 2-8 part, the AS of 1-5 part and the halogenide of 1-5 part; Add in the excess water and mix, under the rotating speed that PM 500-1000 changes, be prepared from stirring reaction 60-100 minute.
Wherein, described long chain fatty acid salt is C 12-C 22Higly branched chain alkyl fatty hydrochlorate.Said C 12-C 22Higly branched chain alkyl fatty hydrochlorate be 2-hydroxyethyl lauric acid.Said AS is a salicylate.Said organosilicon quaternary ammonium salt monomer is formed by tetraethoxy and lauryl amine prepared in reaction, and its mass concentration ratio is 1-3: 2-5.Said halogenide is from NaX, NH 4Select among X, the KX, wherein X is C1 or Br.
Wherein, said organosilicon quaternary ammonium salt monomer is prepared by following method: in the pH value is in the basic soln of 9-12, and adding weight part is tetraethoxy of 1-3 part and the lauryl amine of 2-5 part, through distillation reaction 10-14 hour, after purification by liquid extraction form.
The performance index of break-free fracturing fluid of the present invention are viscosity: 300-1000mPa.s; The highest sand ratio of taking: 60%; Maximum operation (service) temperature: 150 ℃; Level of residue:<0.5%; Core permeability injury:<1%; Anti-shear performance: continuous shear viscosity descended<5% in 120 minutes.
The present invention has following advantage compared with prior art:
1, the molecular weight of all components all is lower than 1000, is a kind of non-polymer system, no residue, and the rate of permeation free of losses to rock core can not cause secondary pollution to the stratum;
2, viscosity does not receive the prolongation of shear time and reduces, and can guarantee construction safety, improves and takes the sand ratio, and this highest of the fracturing fluid use sand ratio can reach 60%;
3, need not to add gel breaker, can be under the effect of in-place oil and local water, dissolving automatically, viscosity drops to below the 5mPa.s, can realize all rows of returning;
4, use temperature is high, can reach 150 ℃.
Five, embodiment
A kind of break-free fracturing fluid, its component and proportioning are following, and said proportioning is a weight part:
Long chain fatty acid salt 1-3 organosilicon quaternary ammonium salt monomer 2-8
AS 1-5 halogenide 1-5 surplus is a water,
Its compound method is: at normal temperatures; With the hard soap of 1-3 part, the organosilicon quaternary ammonium salt monomer of 2-8 part, the AS of 1-5 part and the halogenide of 1-5 part; Add in the excess water and mix, under the rotating speed that PM 500-1000 changes, be prepared from stirring reaction 60-100 minute.
Long chain fatty acid salt is C 12-C 22Higly branched chain alkyl fatty hydrochlorate.Said C 12-C 22Higly branched chain alkyl fatty hydrochlorate be 2-hydroxyethyl lauric acid.Said AS is a salicylate.Said organosilicon quaternary ammonium salt monomer by its mass concentration ratio be 1-3: 2-5 the reaction of tetraethoxy and lauryl amine (how?) be prepared from.Said halogenide is from NaX, NH 4Select among X, the KX, wherein X is Cl or Br.
Organosilicon quaternary ammonium salt monomer compound method is: in the basic soln of 9-12, add tetraethoxy of 1-3 part and the lauryl amine of 2-5 part in the pH value, through distillation reaction 10-14 hour, after purification by liquid extraction form.
Provide specific embodiment below the present invention:
Embodiment one
2 parts of organosilicon quaternary ammonium salt monomers, 1 part of 2-hydroxyethyl lauric acid, 0.5 part of SS and 0.5 part of KCl are joined in 96 parts of water, and stirring reaction was prepared from 60 minutes under the speed that PM 500 changes.The break-free fracturing fluid for preparing can reach under the viscosity normal temperature about 600mPa.s, and bottom temperature (below 70 ℃) viscosity down can reach 300-600mPa.s, can satisfy the construction needs.
The monomeric preparation method of organosilicon quaternary ammonium salt is: in the pH value is 9 basic soln, add 1 part tetraethoxy and 2 parts lauryl amine, through distillation reaction 10 hours, after purification by liquid extraction form.
Embodiment two
5 parts organosilicon quaternary ammonium salt monomers, 2 parts 2-hydroxyethyl 16 carbonic acid or 2-hydroxyethyl 18 carbonic acid, 1 part SS and 2 parts KBr are joined in 90 parts of water, under the speed that PM 700 changes, mix and be prepared from 40 minutes.Can reach about 800mPa.s under the break-free fracturing fluid viscosity normal temperature for preparing, bottom temperature (70 ℃-120 ℃) viscosity down can reach 300-600mPa.s, can satisfy the needs of construction.
The monomeric preparation method of organosilicon quaternary ammonium salt is: in the pH value is 11 basic soln, add 2 parts tetraethoxy and 3 parts lauryl amine, through distillation reaction 12 hours, after purification by liquid extraction form.
Embodiment three
8 parts of organosilicon quaternary ammonium salt monomers, 3 parts of 2-hydroxyethyl 18 carbonic acid, 2 parts of SSs and 3 parts of KCl are joined in 84 parts of water, under the speed that PM 1000 changes, mix and be prepared from 60 minutes.Can reach about 1000mPa.s under the fracturing liquid viscosity normal temperature for preparing, bottom temperature (120-150 ℃) viscosity down can reach 400-600mPa.s, can satisfy the construction needs.
The monomeric preparation method of organosilicon quaternary ammonium salt is: in the pH value is 12 basic soln, add 3 parts tetraethoxy and 5 parts lauryl amine, through distillation reaction 14 hours, after purification by liquid extraction form.
The technical indicator of the break-free fracturing fluid that various embodiments of the present invention prepare is following:
Viscosity 300-1000mPa.s; The highest sand of taking is than 60%; 150 ℃ of maximum operation (service) temperatures; 120 minutes continuous shear viscosities of anti-shear performance descend<5%; Level of residue<0.5%; Core permeability injury<1%.

Claims (3)

1. break-free fracturing fluid; It is characterized in that preparing: 2 parts of organosilicon quaternary ammonium salt monomers, 1 part of 2-hydroxyethyl lauric acid, 0.5 part of SS and 0.5 part of KCl are joined in 96 parts of water by following method; Stirring reaction was prepared from 60 minutes under the speed that PM 500 changes, and can reach 600mPa.s under the said break-free fracturing fluid viscosity normal temperature, and bottom temperature viscosity below 70 ℃ the time can reach 300-600mPa.s; The monomeric preparation method of wherein said organosilicon quaternary ammonium salt is: in the pH value is 9 basic soln; Add 1 part tetraethoxy and 2 parts lauryl amine, through distillation reaction 10 hours, after purification by liquid extraction form.
2. break-free fracturing fluid; It is characterized in that preparing: 5 parts organosilicon quaternary ammonium salt monomers, 2 parts 2-hydroxyethyl 16 carbonic acid or 2-hydroxyethyl 18 carbonic acid, 1 part SS and 2 parts KBr are joined in 90 parts of water by following method; Under the speed that PM 700 changes, mix and be prepared from 40 minutes; Can reach 800mPa.s under the said break-free fracturing fluid viscosity normal temperature; Bottom temperature viscosity in the time of 70 ℃-120 ℃ can reach 300-600mPa.s, and the monomeric preparation method of wherein said organosilicon quaternary ammonium salt is: in the pH value is 11 basic soln, add 2 parts tetraethoxy and 3 parts lauryl amine; Through distillation reaction 12 hours, after purification by liquid extraction form.
3. break-free fracturing fluid; It is characterized in that preparing: 8 parts of organosilicon quaternary ammonium salt monomers, 3 parts of 2-hydroxyethyl 18 carbonic acid, 2 parts of SSs and 3 parts of KCl are joined in 84 parts of water by following method; Under the speed that PM 1000 changes, mix and be prepared from 60 minutes, can reach 1000mPa.s under the said break-free fracturing fluid viscosity normal temperature, viscosity can reach 400-600mPa.s when bottom temperature was 120-150 ℃; The monomeric preparation method of wherein said organosilicon quaternary ammonium salt is: in the pH value is 12 basic soln; Add 3 parts tetraethoxy and 5 parts lauryl amine, through distillation reaction 14 hours, after purification by liquid extraction form.
CN 201010157881 2010-04-22 2010-04-22 Break-free fracturing fluid Active CN101805601B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 201010157881 CN101805601B (en) 2010-04-22 2010-04-22 Break-free fracturing fluid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 201010157881 CN101805601B (en) 2010-04-22 2010-04-22 Break-free fracturing fluid

Publications (2)

Publication Number Publication Date
CN101805601A CN101805601A (en) 2010-08-18
CN101805601B true CN101805601B (en) 2012-12-05

Family

ID=42607556

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 201010157881 Active CN101805601B (en) 2010-04-22 2010-04-22 Break-free fracturing fluid

Country Status (1)

Country Link
CN (1) CN101805601B (en)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101362943A (en) * 2008-09-15 2009-02-11 青岛生物能源与过程所 Preparation of novel thermal resistant and shearing resistant clean fracturing fluid thickener by long chain quaternary ammonium salt containing 18-40 carbon number

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX2010006418A (en) * 2007-12-12 2010-11-25 M I Drilling Fluids Uk Ltd Invert silicate fluids for wellbore strengthening.

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101362943A (en) * 2008-09-15 2009-02-11 青岛生物能源与过程所 Preparation of novel thermal resistant and shearing resistant clean fracturing fluid thickener by long chain quaternary ammonium salt containing 18-40 carbon number

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
吴琼等.FPF清洁无聚携砂液的研制与应用.《钻井液与完井液》.2007,第24卷(第3期),p55-56以及p63、p93. *
赵福麟.采油用化学剂的研究进展.《中国石油大学学报(自然科学版)》.2007,第31卷(第1期),p163-172. *

Also Published As

Publication number Publication date
CN101805601A (en) 2010-08-18

Similar Documents

Publication Publication Date Title
CN108929669B (en) Recoverable clean fracturing fluid thickening agent, preparation method and recovery method thereof, and high-temperature-resistant clean fracturing fluid
CN101845301B (en) Clean fracturing fluid thickener and preparation method thereof
CN102634328B (en) Carboxymethyl hydroxypropyl guanidine gum fracturing fluid
CN101314713A (en) Controllable-viscosity acid liquor system for carbonatite container horizon acid fracturing
CN104710974A (en) Oligomer surfactant clean fracturing fluid and preparation method thereof
CN104177534B (en) A kind of cationic polymer thickening agent, fracturing fluid and preparation method thereof
CN105238381B (en) A kind of function composite lotion state polymer fracturing fluid and preparation method thereof
RU2722804C1 (en) Thickener based on a cationic polymer, a method for production thereof and a heat-resistant fluid for hydraulic fracturing of a formation, obtained using it
CN103819609A (en) Low-friction-resistance high-temperature-resistant gelled acid and preparation method thereof
CN106939158B (en) Temperature-resistant and salt-resistant polymer oil-displacing agent and preparation method thereof
CN110665431A (en) Preparation of sulfonic acid amphoteric gemini viscoelastic surfactant and application of surfactant in fracturing fluid
CN103820099A (en) Acid liquor friction reducer and preparation method thereof
CN107118756A (en) A kind of efficient thick-oil thinner and preparation method thereof
CN110801774B (en) Preparation method and application of dication temperature-resistant recoverable surfactant
CN111218268B (en) Slickwater for compact sandstone reservoir and preparation method thereof
CN101805601B (en) Break-free fracturing fluid
CN104449633B (en) A kind of crude oil surfactant and its preparation method and application
CN106687557A (en) Use of encapsulated polyamines for limiting fluid loss
CN103242814B (en) Slow blocking remover for deep part of oil and water well
CN105646775B (en) A kind of hydrophobic associated polymer and preparation method thereof
CN103374344B (en) After a kind of broken glue, there is surface-active fracturing fluid system
CN102757777B (en) Inhibition water locking type high temperature resistant fracturing fluid for tight gas reservoir fracturing
CN105884926B (en) A kind of preparation method of modified hydroxypropyl guar thickening agent
CN109233782B (en) Fracturing fluid suitable for hot water preparation and preparation method thereof
CN103012667B (en) Synthesis method for selective water shutoff agent for water control and sand prevention of oil well

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant