USRE33855E - Terpolymer composition for aqueous drilling fluids - Google Patents
Terpolymer composition for aqueous drilling fluids Download PDFInfo
- Publication number
- USRE33855E USRE33855E US07/286,887 US28688788A USRE33855E US RE33855 E USRE33855 E US RE33855E US 28688788 A US28688788 A US 28688788A US RE33855 E USRE33855 E US RE33855E
- Authority
- US
- United States
- Prior art keywords
- amount
- brown coal
- lignin
- present
- terpolymer
- 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.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 20
- 229920001897 terpolymer Polymers 0.000 title claims abstract description 13
- 239000012530 fluid Substances 0.000 title claims abstract description 12
- 238000005553 drilling Methods 0.000 title claims abstract description 11
- 239000003077 lignite Substances 0.000 claims abstract description 35
- 229920005610 lignin Polymers 0.000 claims abstract description 31
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims abstract description 14
- 229940088644 n,n-dimethylacrylamide Drugs 0.000 claims abstract description 11
- YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000011575 calcium Substances 0.000 claims abstract description 7
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229910052791 calcium Inorganic materials 0.000 claims abstract description 6
- 239000004615 ingredient Substances 0.000 claims abstract description 5
- 238000000034 method Methods 0.000 claims abstract description 5
- 239000003129 oil well Substances 0.000 claims abstract description 5
- 239000004927 clay Substances 0.000 claims abstract description 4
- 238000000518 rheometry Methods 0.000 claims abstract description 4
- 239000012267 brine Substances 0.000 claims abstract description 3
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 claims abstract description 3
- 230000006641 stabilisation Effects 0.000 claims abstract description 3
- 238000011105 stabilization Methods 0.000 claims abstract description 3
- 230000000087 stabilizing effect Effects 0.000 claims abstract description 3
- 239000004021 humic acid Substances 0.000 claims description 9
- 229920001732 Lignosulfonate Polymers 0.000 claims description 8
- 239000000463 material Substances 0.000 claims description 7
- 229920000642 polymer Polymers 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 5
- 239000000178 monomer Substances 0.000 claims description 4
- 230000000379 polymerizing effect Effects 0.000 claims description 2
- FWFUWXVFYKCSQA-UHFFFAOYSA-M sodium;2-methyl-2-(prop-2-enoylamino)propane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(C)(C)NC(=O)C=C FWFUWXVFYKCSQA-UHFFFAOYSA-M 0.000 claims 8
- -1 leonardites Polymers 0.000 claims 4
- 238000006116 polymerization reaction Methods 0.000 abstract description 3
- 229920003169 water-soluble polymer Polymers 0.000 abstract description 2
- 239000000654 additive Substances 0.000 description 9
- 239000000047 product Substances 0.000 description 8
- IRLPACMLTUPBCL-KQYNXXCUSA-N 5'-adenylyl sulfate Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(=O)OS(O)(=O)=O)[C@@H](O)[C@H]1O IRLPACMLTUPBCL-KQYNXXCUSA-N 0.000 description 5
- 230000000996 additive effect Effects 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- WHNPOQXWAMXPTA-UHFFFAOYSA-N 3-methylbut-2-enamide Chemical compound CC(C)=CC(N)=O WHNPOQXWAMXPTA-UHFFFAOYSA-N 0.000 description 2
- QJZYHAIUNVAGQP-UHFFFAOYSA-N 3-nitrobicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid Chemical compound C1C2C=CC1C(C(=O)O)C2(C(O)=O)[N+]([O-])=O QJZYHAIUNVAGQP-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000013505 freshwater Substances 0.000 description 2
- 239000013535 sea water Substances 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- 229920000536 2-Acrylamido-2-methylpropane sulfonic acid Polymers 0.000 description 1
- XHZPRMZZQOIPDS-UHFFFAOYSA-N 2-Methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid Chemical compound OS(=O)(=O)CC(C)(C)NC(=O)C=C XHZPRMZZQOIPDS-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical class [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- 101001105683 Homo sapiens Pre-mRNA-processing-splicing factor 8 Proteins 0.000 description 1
- 102100021231 Pre-mRNA-processing-splicing factor 8 Human genes 0.000 description 1
- 101000862778 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) 40S ribosomal protein S3 Proteins 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 1
- 239000010428 baryte Substances 0.000 description 1
- 229910052601 baryte Inorganic materials 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 229920005601 base polymer Polymers 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 229910052622 kaolinite Inorganic materials 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- ARQTVSWBVIWYSF-UHFFFAOYSA-N prop-2-enamide;prop-2-enenitrile Chemical compound C=CC#N.NC(=O)C=C ARQTVSWBVIWYSF-UHFFFAOYSA-N 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 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
- C09K8/84—Compositions based on water or polar solvents
- C09K8/86—Compositions based on water or polar solvents containing organic compounds
- C09K8/88—Compositions based on water or polar solvents containing organic compounds macromolecular compounds
- C09K8/90—Compositions based on water or polar solvents containing organic compounds macromolecular compounds of natural origin, e.g. polysaccharides, cellulose
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/52—Amides or imides
- C08F220/54—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide
- C08F220/58—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide containing oxygen in addition to the carbonamido oxygen, e.g. N-methylolacrylamide, N-(meth)acryloylmorpholine
- C08F220/585—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide containing oxygen in addition to the carbonamido oxygen, e.g. N-methylolacrylamide, N-(meth)acryloylmorpholine and containing other heteroatoms, e.g. 2-acrylamido-2-methylpropane sulfonic acid [AMPS]
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F289/00—Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds not provided for in groups C08F251/00 - C08F287/00
-
- 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
- C09K8/02—Well-drilling compositions
- C09K8/04—Aqueous well-drilling compositions
- C09K8/14—Clay-containing compositions
- C09K8/18—Clay-containing compositions characterised by the organic compounds
- C09K8/22—Synthetic organic compounds
- C09K8/24—Polymers
Definitions
- Resinex a sulfonated lignite complexed with a sulfonated phenolic resin, is a commercially available high temperature, high pressure fluid loss additive for drilling muds. It is effective in controlling filtration properties in both fresh sea water muds with high concentrations of soluble calcium.
- a method for improving high temperature fluid loss and rheology stabilization of high calcium brine clay-containing oil well drilling fluids which comprises adding thereto a stabilizing amount of a water-soluble terpolymer composition comprising: polymer prepared by polymerizing the following monomer ingredients:
- compositions containing lignin, modified lignin, brown coal or modified brown coal in an amount ranging between 5-95% with the lignin, modified lignin, brown coal or modified brown coal having been present during the polymerization of the water-soluble polymer.
- lignite is a brown coal in which the original structure of the wood is still recognizable. It is commonly known that lignite may be reacted with sulfuric acid or SO 3 to produce a sulfonated lignite.
- SO 3 sulfuric acid
- lignin is a byproduct formed in the processing of wood for the manufacture of paper.
- leonardite is a naturally oxidized product with higher oxygen and moisture content than lignite.
- humic acid which is a complexed polycyclic polycarboxylic acid which can be converted into its salt form e.g. alkali metal, ammonia or amine, or it can be sulfonated.
- salt form e.g. alkali metal, ammonia or amine
- sulfonated e.g. sodium bicarbonate
- Such products as well as other derivatives of humic acid are described in U.S. Pat. No. 3,266,887. The disclosure of which is incorporated herein by reference.
- the polymer portion of the compostion used to practice the invention is prepared in accordance with the teachings of U.S. Pat. No. 4,502,964.
- the reaction temperature and times may be varied with the reaction time being temperature dependent, e.g. the higher the temperature the shorter the reaction time. Generally, temperatures within the range of about 35°-80° C. may be employed. Although, the temperature and reaction times vary, they are further governed by the amount of catalyst as well as the ratio of the reactants. Often, routine experimentation must be used to optimize the process.
- compositions are prepared by conducting the polymerization in the presence of the lignin, modified lignin, brown coal or modified brown coal.
- the amount of brown coal combined with the polymer as indicated ranges between 5-95%, preferably 20-50% and most preferably 20-35% by weight.
- One of the surprising facts of the invention is that the entire broad range of lignin, modified lignin, brown coal or modified brown coal used shows excellent results are achieved in providing fluid loss control.
- composition of this invention provides good results at dosages ranging between 0.5-10 lbs. per barrel.
- a preferred dosage range is between 1-5 lbs. per barrel.
- the dosages are varied depending upon the conditions and type of formation being treated.
- the products of the invention provided effective and improved performance as fluid loss additive in oil field drilling fluid. These products show especially improved performance at elevated temperatures.
- These additives may be used in a wide range of drilling fluid types including the following:
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Dispersion Chemistry (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
Abstract
______________________________________
Description
______________________________________
Mole %
Ingredients Preferred General
______________________________________
2-acrylamido-2-methylpropane-
53.5 51-59
sulfonic acid, sodium salt (AMPS.sup.1)
N,N-dimethylacrylamide
16.6 6-28
acrylonitrile 29.8 20-35
______________________________________
.sup.1 AMPS, a registered trademark of Lubrisol, Inc., is
2acrylamido-2-methylpropane sulfonic acid. Na salt.
______________________________________
Ingredients % by weight
______________________________________
NaAMPS 72-3.8
N,N-dimethylacrylamide
13.5-0.7
Acrylonitrile 9.5-0.5
______________________________________
______________________________________
Method of Preparing the Compositions of the Invention
Composition I
Component Weight Percent
______________________________________
(1) Deionized Water 55.77
(2) Causticized Lignite
9.53
(3) 50% Na AMPS Solution
28.87
(4) Dimethylacrylamide
2.71
(5) Acrylonitrile 1.90
(6) EDTA .10
(7) Sodium Bisulfite
.56
(8) Ammonium Persulfate
.56
100.00
______________________________________
______________________________________ Monomer Residual ______________________________________ ACN 1.7 μg/g AMPS .07% diMeAcAM <.05% ______________________________________
TABLE I
______________________________________
Product Compositions
Weight Percents
Composition N,N-dimethyl- Lig-
No. NaAMPS acrylamide Acrylonitrile
nite
______________________________________
1 50.5 9.5 6.7 33.3
2 60.7 11.4 7.9 20
3 72.0 13.5 9.5 5
4 3.8 0.7 0.5 95
5 54.3 12.4 -- 33.3
6 47.2 18.4 1.1 33.3
7 48.6 14.7 3.4 33.3
8 51.6 6.7 8.4 33.3
9 56.9 2.1 7.7 33.3
10 59.3 -- 7.4 33.3
11 66.7 -- -- 33.3
______________________________________
______________________________________ Composition No. Lignin/Lignite Variation ______________________________________ 12 Ca lignosulfonate 13 Na lignosulfonate 14 Lignin 15 Sulfomethylated lignite 16 Sulfonated lignite ______________________________________
______________________________________ 280 g water 15 g bentonite 40 g kaolinite 4 g chrome lignosulfonate 294 g barite 10.6 g sea salt ______________________________________
TABLE II
______________________________________
Composi-
Concentration
HTHP Fluid Loss (ml)
tion No.
(lbs/bbl Unaged Aged 350° F.
______________________________________
Blank -- dry @ 27 min dry @ 28 min
1 2 80 70
2 2 64 62
3 2 76 66
4 2 142 134
5 2 90 70
6 2 78 60
7 2 74 62
8 2 96 66
9 2 98 94
10 2 112 94
11 2 84 70
12 2 dry @ 29 min 30 sec
82
13 2 134 102
14 2 dry @ 27 min 96
15 2 dry @ 29 min 30 sec
124
16 2 124 96
______________________________________
Claims (3)
- 20-35% by weight..]. .Iadd.4. A composition comprising:terpolymer segments comprising units derived from acrylonitrile, N,N-dimethylacrylamide, and 2-acrylamido-2-methylpropane sulfonic acid, sodium salt wherein said acrylonitrile is present in an amount up to about 9.5%, said N,N-dimethyacrylamide is present in an amount up to about 18.4% and said 2-acrylamido-2-methylpropane sulfonic acid, sodium salt is present in an amount of about 3.8% to about 72%;from about 5% to about 95% by weight of a lignin, modified lignin, brown coal or modified brown coal selected from the group consisting of lignites, sulfonated lignites, lignins, leonardites, lignosulfonates, humic acids, sulfonated humic acids, and the salts of each;said terpolymer segments being formed in the presence of said material.
- .Iaddend. .Iadd.5. A composition comprising:terpolymer segments comprising units derived from acrylonitrile, N,N-dimethylacrylamide, and 2-acrylamido-2-methylpropane sulfonic acid, sodium salt wherein said acrylonitrile is present in an amount up to about 9.5%, said N,N-dimethylacrylamide is present in an amount up to about 18.4%, and said 2-acrylamido-2-methylpropane sulfonic acid, sodium salt is present in an amount of about 3.8% to about 72%;from about 20% to about 35% by weight of a lignin, modified lignin, brown coal or modified brown coal selected from the group consisting of lignites, sulfonated lignites, lignins, leonardites, lignosulfonates, humic acids, sulfonated humic acids, and the salts of each;said terpolymer segments being formed in the presence of said material.
- .Iaddend. .Iadd.6. A composition comprising:terpolymer segments comprising units derived from acrylonitrile, N,N-dimethylacrylamide, and 2-acrylamido-2-methylpropane sulfonic acid, sodium salt, wherein said acrylonitrile is present in an amount of at least about 0.5% to about 9.5%, said N,N-dimethylacrylamide is present in an amount of at least about 0.7% to about 13.5% and said 2-acrylamido-2-methylpropane sulfonic acid, sodium salt is present in an amount of at least about 3.8% to about 72%;from about 5% to about 95% by weight of a lignin, modified lignin, brown coal or modified brown coal selected from the group consisting of lignites, sulfonated lignites, lignins, leonardites, lignosulfonates, humic acids, sulfonated humic acids, and the salts of each;said terpolymer segments being formed in the presence of said material. .Iaddend. .Iadd.7. A composition comprising:terpolymer segments comprising units derived from acrylonitrile, N,N-dimethylacrylamide, and 2-acrylamido-2-methylpropane sulfonic acid, sodium salt, wherein said acrylonitrile is present in an amount of at least about 0.5% to about 9.5%, said N,N-dimethylacrylamide is present in an amount of at least about 0.7% to about 13.5% and said 2-acrylamido-2-methylpropane sulfonic acid, sodium salt is present in an amount of at least about 3.8% to about 72%;from about 20% to about 35% by weight of a lignin, modified lignin, brown coal or modified brown coal selected from the group consisting of lignites sulfonated lignites, lignins, leonardites, lignosulfonates, humic acids, sulfonated humic acids, and the salts of each;said terpolymer segments being formed in the presence of said material. .Iaddend.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/286,887 USRE33855E (en) | 1986-04-07 | 1988-12-20 | Terpolymer composition for aqueous drilling fluids |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/848,527 US4678591A (en) | 1986-04-07 | 1986-04-07 | Terpolymer composition for aqueous drilling fluids |
| US07/144,260 USRE33856E (en) | 1986-04-07 | 1988-01-15 | Terpolymer compositions for aqueous drilling fluids |
| US07/286,887 USRE33855E (en) | 1986-04-07 | 1988-12-20 | Terpolymer composition for aqueous drilling fluids |
Related Parent Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/848,527 Reissue US4678591A (en) | 1986-04-07 | 1986-04-07 | Terpolymer composition for aqueous drilling fluids |
| US07/144,260 Division USRE33856E (en) | 1986-04-07 | 1988-01-15 | Terpolymer compositions for aqueous drilling fluids |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USRE33855E true USRE33855E (en) | 1992-03-24 |
Family
ID=27386065
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/286,887 Expired - Lifetime USRE33855E (en) | 1986-04-07 | 1988-12-20 | Terpolymer composition for aqueous drilling fluids |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | USRE33855E (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5728653A (en) * | 1992-01-31 | 1998-03-17 | Institut Francais Du Petrole | Method for inhibiting reactive argillaceous formations and use thereof in a drilling fluid |
| CN114891489A (en) * | 2022-03-24 | 2022-08-12 | 长江大学 | Non-sulfonated high-temperature-resistant water-based drilling fluid |
Citations (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2650197A (en) * | 1953-04-21 | 1953-08-25 | Henry W Rahn | Well drilling composition and method of manufacture thereof |
| US2718497A (en) * | 1950-11-03 | 1955-09-20 | Union Oil Co | Drilling muds |
| US2935504A (en) * | 1955-10-10 | 1960-05-03 | Puget Sound Pulp And Timber Co | Process of improving the effectiveness of the components of spent sulfite liquor andthe products thereof |
| US3266887A (en) * | 1962-10-29 | 1966-08-16 | Nalco Chemical Co | Ore pelletization process and products |
| US3639263A (en) * | 1968-07-31 | 1972-02-01 | Nalco Chemical Co | Corrosion inhibition with a tannin, cyanohydrinated lignosulfonate, and an inorganic metal salt composition |
| US3700728A (en) * | 1968-01-04 | 1972-10-24 | Canadian Patents Dev | Solubilization of humic acids, lignites and coals |
| US3985659A (en) * | 1975-02-24 | 1976-10-12 | Georgia-Pacific Corporation | Drilling fluid composition |
| US4374738A (en) * | 1980-06-09 | 1983-02-22 | Georgia-Pacific Corporation | Drilling fluid composition |
| EP0072445A2 (en) * | 1981-07-27 | 1983-02-23 | B W Mud Limited | Temperature stable drilling fluids |
| US4502964A (en) * | 1983-09-09 | 1985-03-05 | Nalco Chemical Company | Terpolymers for use as high temperature fluid loss additive and rheology stabilizer for high pressure, high temperature oil well drilling fluids |
| US4502966A (en) * | 1983-09-09 | 1985-03-05 | Nalco Chemical Company | Terpolymers for use as high temperature fluid loss additive and rheology stabilizer for high pressure, high temperature oil well drilling fluids |
| US4502965A (en) * | 1983-09-09 | 1985-03-05 | Nalco Chemical Company | Terpolymers for use as high temperature fluid loss additive and rheology stabilizer for high pressure, high temperature oil well drilling fluids |
| US4547299A (en) * | 1984-03-15 | 1985-10-15 | Milchem Incorporated | Drilling fluid containing a copolymer filtration control agent |
| US4650593A (en) * | 1977-09-19 | 1987-03-17 | Nl Industries, Inc. | Water-based drilling fluids having enhanced fluid loss control |
| US4676317A (en) * | 1986-05-13 | 1987-06-30 | Halliburton Company | Method of reducing fluid loss in cement compositions which may contain substantial salt concentrations |
-
1988
- 1988-12-20 US US07/286,887 patent/USRE33855E/en not_active Expired - Lifetime
Patent Citations (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2718497A (en) * | 1950-11-03 | 1955-09-20 | Union Oil Co | Drilling muds |
| US2650197A (en) * | 1953-04-21 | 1953-08-25 | Henry W Rahn | Well drilling composition and method of manufacture thereof |
| US2935504A (en) * | 1955-10-10 | 1960-05-03 | Puget Sound Pulp And Timber Co | Process of improving the effectiveness of the components of spent sulfite liquor andthe products thereof |
| US3266887A (en) * | 1962-10-29 | 1966-08-16 | Nalco Chemical Co | Ore pelletization process and products |
| US3700728A (en) * | 1968-01-04 | 1972-10-24 | Canadian Patents Dev | Solubilization of humic acids, lignites and coals |
| US3639263A (en) * | 1968-07-31 | 1972-02-01 | Nalco Chemical Co | Corrosion inhibition with a tannin, cyanohydrinated lignosulfonate, and an inorganic metal salt composition |
| US3985659A (en) * | 1975-02-24 | 1976-10-12 | Georgia-Pacific Corporation | Drilling fluid composition |
| US4650593A (en) * | 1977-09-19 | 1987-03-17 | Nl Industries, Inc. | Water-based drilling fluids having enhanced fluid loss control |
| US4374738A (en) * | 1980-06-09 | 1983-02-22 | Georgia-Pacific Corporation | Drilling fluid composition |
| EP0072445A2 (en) * | 1981-07-27 | 1983-02-23 | B W Mud Limited | Temperature stable drilling fluids |
| US4502964A (en) * | 1983-09-09 | 1985-03-05 | Nalco Chemical Company | Terpolymers for use as high temperature fluid loss additive and rheology stabilizer for high pressure, high temperature oil well drilling fluids |
| US4502966A (en) * | 1983-09-09 | 1985-03-05 | Nalco Chemical Company | Terpolymers for use as high temperature fluid loss additive and rheology stabilizer for high pressure, high temperature oil well drilling fluids |
| US4502965A (en) * | 1983-09-09 | 1985-03-05 | Nalco Chemical Company | Terpolymers for use as high temperature fluid loss additive and rheology stabilizer for high pressure, high temperature oil well drilling fluids |
| US4547299A (en) * | 1984-03-15 | 1985-10-15 | Milchem Incorporated | Drilling fluid containing a copolymer filtration control agent |
| US4676317A (en) * | 1986-05-13 | 1987-06-30 | Halliburton Company | Method of reducing fluid loss in cement compositions which may contain substantial salt concentrations |
Non-Patent Citations (2)
| Title |
|---|
| American Petroleum Institute, publication RP 13(B), 6th ed., Apr. 1976, pp. 1 33, Standard Procedure for Testing Drilling Fluids . * |
| American Petroleum Institute, publication RP 13(B), 6th ed., Apr. 1976, pp. 1-33, "Standard Procedure for Testing Drilling Fluids". |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5728653A (en) * | 1992-01-31 | 1998-03-17 | Institut Francais Du Petrole | Method for inhibiting reactive argillaceous formations and use thereof in a drilling fluid |
| CN114891489A (en) * | 2022-03-24 | 2022-08-12 | 长江大学 | Non-sulfonated high-temperature-resistant water-based drilling fluid |
| CN114891489B (en) * | 2022-03-24 | 2023-10-10 | 长江大学 | Non-sulfonated high-temperature-resistant water-based drilling fluid |
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