CN108611082A - Clean fracturing fluid and preparation method thereof - Google Patents
Clean fracturing fluid and preparation method thereof Download PDFInfo
- Publication number
- CN108611082A CN108611082A CN201611147613.3A CN201611147613A CN108611082A CN 108611082 A CN108611082 A CN 108611082A CN 201611147613 A CN201611147613 A CN 201611147613A CN 108611082 A CN108611082 A CN 108611082A
- Authority
- CN
- China
- Prior art keywords
- parts
- fracturing fluid
- weight
- clean fracturing
- container
- 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
Links
- 239000012530 fluid Substances 0.000 title claims abstract description 64
- 238000002360 preparation method Methods 0.000 title claims abstract description 13
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims abstract description 51
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 46
- FSWDLYNGJBGFJH-UHFFFAOYSA-N n,n'-di-2-butyl-1,4-phenylenediamine Chemical compound CCC(C)NC1=CC=C(NC(C)CC)C=C1 FSWDLYNGJBGFJH-UHFFFAOYSA-N 0.000 claims abstract description 29
- 235000019270 ammonium chloride Nutrition 0.000 claims abstract description 25
- 239000003093 cationic surfactant Substances 0.000 claims abstract description 20
- 239000011734 sodium Substances 0.000 claims description 43
- 229910052708 sodium Inorganic materials 0.000 claims description 43
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 42
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical group [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 claims description 24
- 239000000203 mixture Substances 0.000 claims description 14
- 238000003756 stirring Methods 0.000 claims description 14
- 239000000243 solution Substances 0.000 claims description 11
- 239000007864 aqueous solution Substances 0.000 claims description 9
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 4
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- AISMNBXOJRHCIA-UHFFFAOYSA-N trimethylazanium;bromide Chemical compound Br.CN(C)C AISMNBXOJRHCIA-UHFFFAOYSA-N 0.000 claims 4
- 239000003795 chemical substances by application Substances 0.000 abstract description 9
- ABBQHOQBGMUPJH-UHFFFAOYSA-M Sodium salicylate Chemical compound [Na+].OC1=CC=CC=C1C([O-])=O ABBQHOQBGMUPJH-UHFFFAOYSA-M 0.000 abstract description 3
- 230000008901 benefit Effects 0.000 abstract description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 8
- 239000007788 liquid Substances 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 239000003963 antioxidant agent Substances 0.000 description 6
- 230000003078 antioxidant effect Effects 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 238000010008 shearing Methods 0.000 description 6
- 239000004094 surface-active agent Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- -1 Cetyl trimethyl bromine Chemical compound 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000031709 bromination Effects 0.000 description 3
- 238000005893 bromination reaction Methods 0.000 description 3
- 150000001768 cations Chemical class 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 235000019441 ethanol Nutrition 0.000 description 3
- 125000001165 hydrophobic group Chemical group 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000002562 thickening agent Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 230000003213 activating effect Effects 0.000 description 2
- 238000005660 chlorination reaction Methods 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 239000002734 clay mineral Substances 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 230000000855 fungicidal effect Effects 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- LODHFNUFVRVKTH-ZHACJKMWSA-N 2-hydroxy-n'-[(e)-3-phenylprop-2-enoyl]benzohydrazide Chemical compound OC1=CC=CC=C1C(=O)NNC(=O)\C=C\C1=CC=CC=C1 LODHFNUFVRVKTH-ZHACJKMWSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241000283153 Cetacea Species 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000219000 Populus Species 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-N Salicylic acid Natural products OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 229920001284 acidic polysaccharide Polymers 0.000 description 1
- 150000004805 acidic polysaccharides Chemical class 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 125000005211 alkyl trimethyl ammonium group Chemical group 0.000 description 1
- SWLVFNYSXGMGBS-UHFFFAOYSA-N ammonium bromide Chemical compound [NH4+].[Br-] SWLVFNYSXGMGBS-UHFFFAOYSA-N 0.000 description 1
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000003064 anti-oxidating effect Effects 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 210000000170 cell membrane Anatomy 0.000 description 1
- 229960002798 cetrimide Drugs 0.000 description 1
- 229960000800 cetrimonium bromide Drugs 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000002068 microbial inoculum Substances 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 150000007523 nucleic acids Chemical class 0.000 description 1
- 102000039446 nucleic acids Human genes 0.000 description 1
- 108020004707 nucleic acids Proteins 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 229960004025 sodium salicylate Drugs 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/60—Compositions for stimulating production by acting on the underground formation
- C09K8/62—Compositions for forming crevices or fractures
- C09K8/66—Compositions based on water or polar solvents
- C09K8/68—Compositions based on water or polar solvents containing organic compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2208/00—Aspects relating to compositions of drilling or well treatment fluids
- C09K2208/12—Swell inhibition, i.e. using additives to drilling or well treatment fluids for inhibiting clay or shale swelling or disintegrating
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)
- Compositions Of Macromolecular Compounds (AREA)
- Detergent Compositions (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
The invention provides a clean fracturing fluid and a preparation method thereof, wherein the clean fracturing fluid comprises the following components in parts by weight: 2-4.5 parts of cationic surfactant, 0.7-1.2 parts of sodium ortho-hydroxybenzoate, 6-9 parts of ammonium chloride, 0.06-0.1 part of N, N' -di-sec-butyl-p-phenylenediamine and 85.2-91.24 parts of water. The clean fracturing fluid provided by the invention has the advantages of low concentration of the main agent, low cost, excellent gel, temperature resistance and shear resistance, and expanded application range.
Description
Technical field
The present invention relates to petroleum industry chemicals technical fields more particularly to a kind of clean fracturing fluid and preparation method thereof.
Background technology
Clean fracturing fluid is a kind of a kind of Solid Free fracturing fluid of the surfactant with chemical industry synthesis as thickener,
It can realize at lower viscosities and take sand seam.Clean fracturing fluid with unique rubber breaker manage, in the earth formation meet water or
Broken glue automatically can be realized by meeting oil, and the water not tolerant for being free of water-insoluble after breaking gel or containing is extremely low, counterincision seam surface and sand
The injury of rock permeability is smaller.Therefore, the application effect of clean fracturing fluid is notable.
Currently, the thickening agent (host agent) of clean fracturing fluid is typically by surfactant obtained from chemical industry synthesis, it is main
Agent concentration is higher (5%~7%), therefore leads to that material quantity is big, production cost is higher.Moreover, the gel of clean fracturing fluid is usual
Viscosity at 50 DEG C~60 DEG C suddenly declines, and causes heat resistance poor.Therefore, the higher production cost of clean fracturing fluid
And poor heat resistance, cause the application range of clean fracturing fluid to receive certain limitation.
Invention content
A kind of clean fracturing fluid of present invention offer and preparation method thereof, reduces cost, improves gel and heatproof is cut
Performance is cut, the scope of application of clean fracturing fluid is expanded.
Clean fracturing fluid provided by the invention includes the component of following parts by weight:2~4.5 parts of cationic surfactant,
0.7~1.2 part of septichen sodium, 0.06~0.1 part of 6~9 parts of ammonium chloride, N, N '-di-sec-butyl-p-phenyl enediamine, water 85.2
~91.24 parts.
Wherein, cationic surfactant refers to the surface that hydrophobic group is connected by covalent bond with positively charged hydrophilic group
Activating agent can dissociate the cation with surface-active in aqueous solution.The hydrophobic group of usual cationic surfactant
It is made of the hydroxyl of 8 to 18 carbon, cationic hydrophilic base is by containing the equiatomic group for carrying positive charge of nitrogen phosphate and sulfur or iodine
It constitutes, anionic group is usually single ion or group without surface-active, such as CI-, Br-, Ac-, NO3-.Sun
Ionic surface active agent is in addition to the fundamental property with general surfactant, and cationic surfactant is because hydrophilic group is with just
Charge, and there are some special Interfacial Adsorption performances.
The mechanism of action of the cationic surfactant in fracturing fluid, including it is following aspects:(1) absorption can be selected to obtain
Onto negatively charged microbial inoculum, ion cluster is formed in cell surface, inhibits the function of bacterial membrane, changes the electrical conductance of film, damage
The plasm of evil bacterium, makes natural plant gum class virgin rubber not degrade in the case where placing the long period.(2) it can spread rapidly, soak simultaneously
Oil-water interfaces are adsorbed onto, neutralization interface is electrical, dissolves interfacial film, and the active material in crude oil is made to lose emulsifying capacity.Meanwhile making
The water deviate from emulsion can be assembled, detach quickly.(3) adsorbed film can be formed in gas-liquid or oil-water interfaces, to reduce surface
Or interfacial tension, flow resistance of the liquid in micropore is reduced, liquid is made to be easy to that stratum is discharged.(4) can in clay lattice
Extra negative electrical charge mutually adsorbs, and clay mineral wettability of the surface is made to invert, and forms active agent molecule protective film, prevents moisture
Son enters clay mineral intracell, to reduce the expansion and migration of clay.
Clean fracturing fluid provided by the invention, host agent concentration is low, and production cost is low, and liquid prepares simple, heatproof cutting performance
It is excellent, thus improve the scope of application of clean fracturing fluid.
Optionally, cationic surfactant is cetyl trimethylammonium bromide or octadecyl trimethyl bromination
Ammonium.
In one embodiment, clean fracturing fluid is grouped as by the group of following parts by weight:Cetyl trimethyl bromination
2 parts of ammonium, 0.7 part of septichen sodium, 0.06 part of 6 parts of ammonium chloride, N, N '-di-sec-butyl-p-phenyl enediamine, 91.24 parts of water.
In another embodiment, clean fracturing fluid is grouped as by the group of following parts by weight:Cetyl trimethyl bromine
Change 2.5 parts of ammonium, 0.9 part of septichen sodium, 0.06 part of 7 parts of ammonium chloride, N, N '-di-sec-butyl-p-phenyl enediamine, water 89.54
Part.
In another embodiment, clean fracturing fluid is grouped as by the group of following parts by weight:Octadecyl trimethyl bromine
Change 3 parts of ammonium, 0.9 part of septichen sodium, 0.06 part of 8 parts of ammonium chloride, N, N '-di-sec-butyl-p-phenyl enediamine, 88.04 parts of water.
In another embodiment, clean fracturing fluid is grouped as by the group of following parts by weight:Octadecyl trimethyl bromine
Change 4.5 parts of ammonium, 1.2 parts of septichen sodium, 0.06 part of 9 parts of ammonium chloride, N, N '-di-sec-butyl-p-phenyl enediamine, water 85.24
Part.
Clean fracturing liquid and preparation method thereof provided by the invention, including:
1) water of 85.2~91.24 parts by weight is added in the first container at room temperature;
2) the septichen sodium of 0.7~1.2 parts by weight is added in second container, and is taken from the first container
Second container is added in suitable water, stirs 20min under the speed of 200-300r/min, is configured to a concentration of 10% adjacent hydroxyl
Aqueous sodium benzoate solution;
3) be added in the first container 6~9 parts by weight of ammonium chloride and N, N '-di-sec-butyl-p-phenyl enediamine 0.06~
0.10 parts by weight stir 5min under the speed of 200-300r/min, obtain the first mixture;
4) 2~4.5 parts by weight of cationic surfactant are added in the first container, in the speed of 200-300r/min
Degree is lower to stir 3min, obtains the second mixture;
5) the septichen sodium water solution is added in the first container, under the speed of 200-300r/min
5min is stirred, clean fracturing fluid is obtained.
The implementation of the present invention, at least has the advantage that:
1, the host agent concentration of clean fracturing fluid is low (2%~4.5%), compared to existing concentration (5%~7%), materials
Amount reduces, 40% or more cost reduction.
2, after 80 DEG C of clean fracturing fluid or more shears a hour, viscosity can still reach 100mPa.S or more, improve
The heatproof anti-shear performance of clean fracturing fluid.
Description of the drawings
In order to more clearly explain the embodiment of the invention or the technical proposal in the existing technology, to embodiment or will show below
There is attached drawing needed in technology description to be briefly described, it should be apparent that, the accompanying drawings in the following description is this hair
Some bright embodiments for those of ordinary skill in the art without having to pay creative labor, can be with
Obtain other attached drawings according to these attached drawings.
Fig. 1 is the molecular structure for the cetyl trimethylammonium bromide that the embodiment of the present invention one provides;
Fig. 2 is the molecular structure for the Cetyltrimethylammonium bromide that the embodiment of the present invention one provides.
Specific implementation mode
In order to make the object, technical scheme and advantages of the embodiment of the invention clearer, below in conjunction with the embodiment of the present invention
In attached drawing, technical scheme in the embodiment of the invention is clearly and completely described, it is clear that described embodiment is
A part of the embodiment of the present invention, instead of all the embodiments.Based on the embodiments of the present invention, those of ordinary skill in the art
The every other embodiment obtained without making creative work, shall fall within the protection scope of the present invention.
The source of raw material employed in the following embodiments of the present invention is as follows:
Cetyl trimethylammonium bromide:Xinjiang Urumqi Ke Ruier companies
Cetyltrimethylammonium bromide:Xinjiang Urumqi Ke Ruier companies
Septichen sodium:Xinjiang Urumqi Ke Ruier companies, the photochemical factory in Yixing City Shen
N, N '-di-sec-butyl-p-phenyl enediamine:Nanjing Li Da Chemical Co., Ltd.s
Embodiment one
In the present embodiment, clean fracturing fluid can be grouped as by the group of following parts by weight:Cationic surfactant 2~
4.5 parts, 0.7~1.2 part of septichen sodium, 0.06~0.1 part of 6~9 parts of ammonium chloride, N, N '-di-sec-butyl-p-phenyl enediamine,
85.2~91.24 parts of water.
Wherein, cationic surfactant refers to the surface that hydrophobic group is connected by covalent bond with positively charged hydrophilic group
Activating agent can dissociate the cation with surface-active in aqueous solution.
Septichen sodium is also referred to as sodium salicylate, poplar acid sodium, salicylic acid sodium, 2 hydroxybenzoic acid sodium etc., for white squama
Piece or powder, odorlessness, pink in long exposure line, soluble easily in water, glycerine can be dissolved in 95% ethyl alcohol, insoluble in ether, chlorine
Imitative, benzene, aqueous solution are in subacidity, molecular formula C7H5NaO3.Septichen sodium is chiefly used in activator.
N, N '-di-sec-butyl-p-phenyl enediamine are also referred to as secondary-butyl-p-phenylenediamine antioxidant, antioxidant 44PD, antioxidant 4720
Deng for brown liquid, no special odor, molecular formula C14H24N2.N, N '-di-sec-butyl-p-phenyl enediamine be chiefly used in antioxidant,
Antioxidant.In the present embodiment, N, N '-di-sec-butyl-p-phenyl enediamine are used as fungicide.
Ammonium chloride is clear crystal or white crystalline powder, and odorless, taste is salty, soluble easily in water, is slightly soluble in ethyl alcohol, molecular formula
For NH4Cl。
Wherein, cationic surfactant act as thickening agent, and septichen sodium act as crosslinking agent, chlorination
Ammonium act as gel stabilizer, N, N '-di-sec-butyl-p-phenyl enediamine act as antioxidant and fungicide.According to each component
Accounting it is different, can adjust clean fracturing fluid Applicable temperature, gelling performance, heatproof be anti-shearing and and anti-oxidation characteristics.
Clean fracturing fluid provided in this embodiment, component include cationic surfactant, septichen sodium, chlorination
Ammonium, N, N '-di-sec-butyl-p-phenyl enediamines and water, the sum of each component weight percent is 100%, due to cationic surfactant
(host agent) concentration is small (2%~4.5%) so that clean fracturing fluid it is of low cost, moreover, by test data, in 80 DEG C of temperature
Viscosity still can reach 100mPa.S or more after degree shearing 1 hour, compared to existing clean fracturing fluid, at low cost and heat resistance
It is good, expand its scope of application.
Optionally, cationic surfactant is cetyl trimethylammonium bromide or octadecyl trimethyl bromination
Ammonium.
Wherein, cetyl trimethylammonium bromide is also referred to as the molten front three of cetrimonium bromide, bromine palm fibre trimethyl ammonium, Cetrimide, whale
Base ammonium bromide etc. is yellow viscous liquid, water-soluble, is slightly soluble in ethyl alcohol, molecular formula C19H42BrN, structural formula C16H33
(CH3)3NBr, point for the cetyl trimethylammonium bromide that molecular structure is provided as shown in FIG. 1, FIG. 1 is the embodiment of the present invention one
Minor structure figure.
Cetyl trimethylammonium bromide is a kind of cationic surfactant, can dissolve cell membrane, is had from low ion
The characteristic of precipitate nucleic acids and acidic polysaccharide in the solution of intensity has good with cation, nonionic, amphoteric surfactant
Compatibility, chemical stability is good, and heat-resisting, fast light, pressure-resistant, strong alkali-acid resistance is chiefly used in lotion foaming agent, surfactant.
Wherein, the molecular formula of Cetyltrimethylammonium bromide is C21H46BrN, structural formula C18H37(CH3)3NBr, point
Minor structure is as shown in Fig. 2, Fig. 2 is the molecular structure for the Cetyltrimethylammonium bromide that the embodiment of the present invention one provides.Ten
The effect of eight alkyl trimethyl ammonium bromides and similar to cetyl trimethylammonium bromide, details are not described herein.
Clean fracturing fluid provided in this embodiment, specific preparation process are as follows:
1) water of 85.2~91.24 parts by weight is added in the first container at room temperature.
2) the septichen sodium of 0.7~1.2 parts by weight is added in second container, and is taken in right amount from the first container
Water be added second container, stir 20min under the speed of 200-300r/min, be configured to a concentration of 10% o-hydroxy first
Acid sodium aqueous solution.
3) 6~9 parts by weight of ammonium chloride and N, N '-di-sec-butyl-p-phenyl enediamine 0.06~0.10 are added in the first container
Parts by weight stir 5min under the speed of 200-300r/min, obtain the first mixture.
4) 2~4.5 parts by weight of cationic surfactant are added in the first container, under the speed of 200-300r/min
3min is stirred, the second mixture is obtained.
5) septichen sodium water solution is added in the first container, is stirred under the speed of 200-300r/min
5min obtains clean fracturing fluid.
Wherein, the sum of weight percent of each component is 100%, when preparing clean fracturing fluid, in the weight of each component
Weight needed for being calculated in range is simultaneously prepared according to the method described above.
Wherein, the first container and second container can be the container with blender also needs in addition, in preparation process
Graduated cylinder, pipette, day equality instrument are taken, to obtain accurate component ratio.
A kind of clean fracturing fluid is present embodiments provided, includes the component of following parts by weight, cationic surfactant 2~
4 parts, 0.7~1.2 part of septichen sodium, 0.06~0.1 part of 6~9 parts of ammonium chloride, N, N '-di-sec-butyl-p-phenyl enediamine, water
85.2~91.24 parts.Clean fracturing fluid provided in this embodiment, the host agent ratio of clean fracturing fluid can be reduced to 2%~
4.5% so that clean fracturing fluid it is of low cost, and improve gel and heatproof cutting performance, expand clean fracturing
The scope of application of liquid.
Embodiment two
In the present embodiment, clean fracturing fluid is grouped as by the group of following parts by weight:Cetyl trimethylammonium bromide 2
Part, 0.7 part of septichen sodium, 0.06 part of 6 parts of ammonium chloride, N, N '-di-sec-butyl-p-phenyl enediamine, 91.24 parts of water.
Clean fracturing fluid provided in this embodiment, specific preparation process are as follows:
1) water of 91.24 parts by weight is added in the first container at room temperature.
2) the septichen sodium of 0.7 parts by weight is added in container second, and takes suitable water from the first container
Second container is added, stirs 20min under the speed of 200-300r/min, is configured to a concentration of 10% septichen sodium
Aqueous solution.
3) 6 parts by weight of ammonium chloride and 0.06 parts by weight of N, N '-di-sec-butyl-p-phenyl enediamine are added in container first,
5min is stirred under the speed of 200-300r/min, obtains the first mixture.
4) 2 parts by weight of cetyl trimethylammonium bromide are added in the first container, under the speed of 200-300r/min
3min is stirred, the second mixture is obtained.
5) septichen sodium water solution is added in the first container, is stirred under the speed of 200-300r/min
5min obtains clean fracturing fluid.
Clean fracturing fluid provided in this embodiment, test effect are as follows:
(shear rate is the shearing of 50 DEG C of the clean fracturing lyogel:170S-1) after a hour, viscosity can still reach
More than 100mPa.S.
Embodiment three
In the present embodiment, clean fracturing fluid is grouped as by the group of following parts by weight:Cetyl trimethylammonium bromide 2.5
Part, 0.9 part of septichen sodium, 0.06 part of 7 parts of ammonium chloride, N, N '-di-sec-butyl-p-phenyl enediamine, 89.54 parts of water.
Clean fracturing fluid provided in this embodiment, specific preparation process are as follows:
1) water of 89.54 parts by weight is added in the first container at room temperature.
2) the septichen sodium of 0.9 parts by weight is added in container second, and takes suitable water from the first container
Second container is added, stirs 20min under the speed of 200-300r/min, is configured to a concentration of 10% septichen sodium
Aqueous solution.
3) 7 parts by weight of ammonium chloride and 0.06 parts by weight of N, N '-di-sec-butyl-p-phenyl enediamine are added in the first container,
5min is stirred under the speed of 200-300r/min, obtains the first mixture.
4) 2.5 parts by weight of cetyl trimethylammonium bromide are added in the first container, in the speed of 200-300r/min
Lower stirring 3min, obtains the second mixture.
5) septichen sodium water solution is added in the first container, is stirred under the speed of 200-300r/min
5min obtains clean fracturing fluid.
Clean fracturing fluid provided in this embodiment, test effect are as follows:
(shear rate is the shearing of 60 DEG C of the clean fracturing lyogel:170S-1) after a hour, viscosity can still reach
More than 100mPa.S.
Example IV
In the present embodiment, clean fracturing fluid is grouped as by the group of following parts by weight:Cetyltrimethylammonium bromide 3
Part, 0.9 part of septichen sodium, 0.06 part of 8 parts of ammonium chloride, N, N '-di-sec-butyl-p-phenyl enediamine, 88.04 parts of water.
Clean fracturing fluid provided in this embodiment, specific preparation process are as follows:
1) water of 88.04 parts by weight is added in the first container at room temperature.
2) the septichen sodium of 0.9 parts by weight is added in container second, and takes suitable water from the first container
Second container is added, stirs 20min under the speed of 200-300r/min, is configured to a concentration of 10% septichen sodium
Aqueous solution.
3) 8 parts by weight of ammonium chloride and 0.06 parts by weight of N, N '-di-sec-butyl-p-phenyl enediamine are added in the first container,
5min is stirred under the speed of 200-300r/min obtains the first mixture.
4) 3 parts by weight of Cetyltrimethylammonium bromide are added in the first container, under the speed of 200-300r/min
Stirring 3min obtains the second mixture.
5) septichen sodium water solution is added in the first container, 5min is stirred under the speed of 200-300r/min
Obtain clean fracturing fluid.
Clean fracturing fluid provided in this embodiment, test effect are as follows:
(shear rate is the shearing of 70 DEG C of the clean fracturing lyogel:170S-1) after a hour, viscosity can still reach
More than 100mPa.S.
Embodiment five
In the present embodiment, clean fracturing fluid is grouped as by the group of following parts by weight:Cetyltrimethylammonium bromide 4.5
Part, 1.2 parts of septichen sodium, 0.06 part of 9 parts of ammonium chloride, N, N '-di-sec-butyl-p-phenyl enediamine, 85.24 parts of water.
Clean fracturing fluid provided in this embodiment, specific preparation process are as follows:
1) water of 85.24 parts by weight is added in the first container at room temperature.
2) the septichen sodium of 1.2 parts by weight is added in second container, and takes suitable water from the first container
Second container is added, stirs 20min under the speed of 200-300r/min, is configured to a concentration of 10% septichen sodium
Aqueous solution.
3) 9 parts by weight of ammonium chloride and 0.06 parts by weight of N, N '-di-sec-butyl-p-phenyl enediamine are added in the first container,
5min is stirred under the speed of 200-300r/min, obtains the first mixture.
4) 4.5 parts by weight of Cetyltrimethylammonium bromide are added in the first container, in the speed of 200-300r/min
Lower stirring 3min, obtains the second mixture.
5) septichen sodium water solution is added in the first container, is stirred under the speed of 200-300r/min
5min obtains clean fracturing fluid.
Clean fracturing fluid provided in this embodiment, test effect are as follows:
(shear rate is the shearing of 80 DEG C of the clean fracturing lyogel:170S-1) after a hour, viscosity can still reach
More than 100mPa.S.
Finally it should be noted that:The above embodiments are only used to illustrate the technical solution of the present invention., rather than its limitations;To the greatest extent
Present invention has been described in detail with reference to the aforementioned embodiments for pipe, it will be understood by those of ordinary skill in the art that:Its according to
So can with technical scheme described in the above embodiments is modified, either to which part or all technical features into
Row equivalent replacement;And these modifications or replacements, various embodiments of the present invention technology that it does not separate the essence of the corresponding technical solution
The range of scheme.
Claims (7)
1. a kind of clean fracturing fluid, which is characterized in that include the component of following parts by weight:Cationic surfactant 2~4.5
Part, 0.7~1.2 part of septichen sodium, 0.06~0.1 part of 6~9 parts of ammonium chloride, N, N '-di-sec-butyl-p-phenyl enediamine, water
85.2~91.24 parts.
2. clean fracturing fluid according to claim 1, which is characterized in that the cationic surfactant is cetyl
Trimethylammonium bromide or Cetyltrimethylammonium bromide.
3. clean fracturing fluid according to claim 2, which is characterized in that include the component of following parts by weight:Cetyl
2 parts of trimethylammonium bromide, 0.7 part of septichen sodium, 0.06 part of 6 parts of ammonium chloride, N, N '-di-sec-butyl-p-phenyl enediamine, water
91.24 parts.
4. clean fracturing fluid according to claim 2, which is characterized in that include the component of following parts by weight:Cetyl
2.5 parts of trimethylammonium bromide, 0.9 part of septichen sodium, 0.06 part of 7 parts of ammonium chloride, N, N '-di-sec-butyl-p-phenyl enediamine,
89.54 parts of water.
5. clean fracturing fluid according to claim 2, which is characterized in that include the component of following parts by weight:Octadecyl
3 parts of trimethylammonium bromide, 0.9 part of septichen sodium, 0.06 part of 8 parts of ammonium chloride, N, N '-di-sec-butyl-p-phenyl enediamine, water
88.04 parts.
6. clean fracturing fluid according to claim 2, which is characterized in that include the component of following parts by weight:Octadecyl
4.5 parts of trimethylammonium bromide, 1.2 parts of septichen sodium, 0.06 part of 9 parts of ammonium chloride, N, N '-di-sec-butyl-p-phenyl enediamine,
85.24 parts of water.
7. a kind of preparation method using claim 1 to 6 any one of them clean fracturing fluid, which is characterized in that including:
1) water of 85.2~91.24 parts by weight is added in the first container at room temperature;
2) the septichen sodium of 0.7~1.2 parts by weight is added in second container, and is taken in right amount from the first container
Water be added second container, stir 20min under the speed of 200-300r/min, be configured to a concentration of 10% o-hydroxy first
Acid sodium aqueous solution;
3) 6~9 parts by weight of ammonium chloride and N, N '-di-sec-butyl-p-phenyl enediamine 0.06~0.10 are added in the first container
Parts by weight stir 5min under the speed of 200-300r/min, obtain the first mixture;
4) 2~4.5 parts by weight of cationic surfactant are added in the first container, under the speed of 200-300r/min
3min is stirred, the second mixture is obtained;
5) the septichen sodium water solution is added in the first container, is stirred under the speed of 200-300r/min
5min obtains clean fracturing fluid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201611147613.3A CN108611082A (en) | 2016-12-13 | 2016-12-13 | Clean fracturing fluid and preparation method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201611147613.3A CN108611082A (en) | 2016-12-13 | 2016-12-13 | Clean fracturing fluid and preparation method thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
CN108611082A true CN108611082A (en) | 2018-10-02 |
Family
ID=63657228
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201611147613.3A Pending CN108611082A (en) | 2016-12-13 | 2016-12-13 | Clean fracturing fluid and preparation method thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN108611082A (en) |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102453480A (en) * | 2010-10-22 | 2012-05-16 | 中国石油天然气集团公司 | Clean viscous acid for acid fracturing of carbonate reservoir |
CN102757777A (en) * | 2012-06-21 | 2012-10-31 | 中国石油天然气股份有限公司 | Inhibition water-locking type high-temperature-resistant fracturing fluid for fracturing of dense gas reservoir |
CN102994064A (en) * | 2011-09-14 | 2013-03-27 | 孙斌 | Novel clean fracturing fluid for hydraulic fracturing |
CN102994065A (en) * | 2011-09-14 | 2013-03-27 | 何林荣 | Preparation technique of clean fracturing fluid on basis of control on surfactant addition amount |
CN103881688A (en) * | 2014-03-12 | 2014-06-25 | 中国石油天然气股份有限公司 | Low-damage clean fracturing fluid for oil well of oil field and application of low-damage clean fracturing fluid |
CN105368436A (en) * | 2015-11-25 | 2016-03-02 | 中国石油天然气股份有限公司 | Small-molecule clean fracturing fluid and preparation method and application thereof |
CN105419767A (en) * | 2014-09-23 | 2016-03-23 | 中国石油化工股份有限公司 | Novel cleaning fracturing fluid system and preparation method thereof |
CN105505370A (en) * | 2014-09-23 | 2016-04-20 | 中国石油化工股份有限公司 | Clean fracturing fluid and preparation method thereof |
-
2016
- 2016-12-13 CN CN201611147613.3A patent/CN108611082A/en active Pending
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102453480A (en) * | 2010-10-22 | 2012-05-16 | 中国石油天然气集团公司 | Clean viscous acid for acid fracturing of carbonate reservoir |
CN102994064A (en) * | 2011-09-14 | 2013-03-27 | 孙斌 | Novel clean fracturing fluid for hydraulic fracturing |
CN102994065A (en) * | 2011-09-14 | 2013-03-27 | 何林荣 | Preparation technique of clean fracturing fluid on basis of control on surfactant addition amount |
CN102757777A (en) * | 2012-06-21 | 2012-10-31 | 中国石油天然气股份有限公司 | Inhibition water-locking type high-temperature-resistant fracturing fluid for fracturing of dense gas reservoir |
CN103881688A (en) * | 2014-03-12 | 2014-06-25 | 中国石油天然气股份有限公司 | Low-damage clean fracturing fluid for oil well of oil field and application of low-damage clean fracturing fluid |
CN105419767A (en) * | 2014-09-23 | 2016-03-23 | 中国石油化工股份有限公司 | Novel cleaning fracturing fluid system and preparation method thereof |
CN105505370A (en) * | 2014-09-23 | 2016-04-20 | 中国石油化工股份有限公司 | Clean fracturing fluid and preparation method thereof |
CN105368436A (en) * | 2015-11-25 | 2016-03-02 | 中国石油天然气股份有限公司 | Small-molecule clean fracturing fluid and preparation method and application thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Sabhapondit et al. | Water soluble acrylamidomethyl propane sulfonate (AMPS) copolymer as an enhanced oil recovery chemical | |
CA2628509C (en) | Viscoelastic compositions comprising polycationic quaternary ammonium compounds | |
CN103965848B (en) | Composite profile control agent and preparation method thereof | |
CN102155209B (en) | Method for fracturing stratum by acidity viscoelastic fluid | |
CN102732244B (en) | Cross-linking agent for fracturing fluid with ultralow hydroxypropyl guar concentration and fracturing fluid prepared from cross-linking agent | |
CN105368436B (en) | Small-molecule clean fracturing fluid and preparation method and application thereof | |
CN106467734B (en) | Crosslinking agent for fracturing and preparation method thereof | |
CN106497534A (en) | A kind of strengthening foam system built by nano-cellulose | |
CN103820095B (en) | Hydroxysulfobetaine viscoelastic surfactant and application thereof in tertiary oil recovery | |
CN102108295A (en) | Alkaline anionic surfactant fracturing fluid | |
CN104449632B (en) | Anti-oil foaming agent and preparation method thereof | |
BR112015021194B1 (en) | VISCOELASTIC FLUID COMPRISING AT LEAST ONE VISCOELASTIC SURFACANT AND AT LEAST ONE SYNERGIC COTENSOACTIVE AND METHOD OF FRACTURING AN UNDERGROUND FORMATION | |
Li et al. | Organic acid-enhanced viscoelastic surfactant and its application in fracturing fluids | |
CN104559995A (en) | Delayed crosslinking fracturing fluid composition | |
CN104910890A (en) | Organoboron-hydroxypropyl guanidine gum system crosslinking promoter, and preparation method thereof | |
CN110665431A (en) | Preparation of sulfonic acid amphoteric gemini viscoelastic surfactant and application of surfactant in fracturing fluid | |
CN103436245A (en) | Synthetic polymer fracturing fluid for fracturing | |
CN112126422B (en) | Drag reducer with high stability and preparation method and application thereof | |
CN110790959A (en) | Water-soluble phenolic resin crosslinking agent low-temperature rapid gelling and crosslinking promoting agent and preparation method and application thereof | |
Cao et al. | Supramolecular self-assembly of robust, ultra-stable, and high-temperature-resistant viscoelastic worm-like micelles | |
CN106147739A (en) | A kind of pressure break clay stabilizer and preparation method thereof | |
BR112017021825B1 (en) | ADJUVANT COMPOSITION AND METHOD FOR PREPARING A PESTICIDE COMPOSITION | |
CN108611082A (en) | Clean fracturing fluid and preparation method thereof | |
CN104403655A (en) | Novel fracturing fluid for oil field and preparation method thereof | |
CN111718704A (en) | Multifunctional flow promoter and high-temperature-resistant polymer fracturing fluid system |
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 |
Application publication date: 20181002 |
|
RJ01 | Rejection of invention patent application after publication |