NO303582B1 - Geldannende vandige blandinger og anvendelse av blandingene ved utvinnelse av olje fra et oljefelt - Google Patents
Geldannende vandige blandinger og anvendelse av blandingene ved utvinnelse av olje fra et oljefelt Download PDFInfo
- Publication number
- NO303582B1 NO303582B1 NO914555A NO914555A NO303582B1 NO 303582 B1 NO303582 B1 NO 303582B1 NO 914555 A NO914555 A NO 914555A NO 914555 A NO914555 A NO 914555A NO 303582 B1 NO303582 B1 NO 303582B1
- Authority
- NO
- Norway
- Prior art keywords
- mixture
- range
- polymer
- stated
- units
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 58
- 238000011084 recovery Methods 0.000 title description 3
- 229920000642 polymer Polymers 0.000 claims description 72
- 229910021645 metal ion Inorganic materials 0.000 claims description 29
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical group NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
- 230000035699 permeability Effects 0.000 claims description 15
- 238000004132 cross linking Methods 0.000 claims description 11
- 229910052783 alkali metal Inorganic materials 0.000 claims description 10
- 150000001340 alkali metals Chemical class 0.000 claims description 10
- 125000000524 functional group Chemical group 0.000 claims description 9
- 229920000620 organic polymer Polymers 0.000 claims description 9
- 239000000178 monomer Substances 0.000 claims description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
- 125000001424 substituent group Chemical group 0.000 claims description 5
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 2
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims description 2
- RQAKESSLMFZVMC-UHFFFAOYSA-N n-ethenylacetamide Chemical compound CC(=O)NC=C RQAKESSLMFZVMC-UHFFFAOYSA-N 0.000 claims description 2
- OPRIWFSSXKQMPB-UHFFFAOYSA-N 2-methyl-2-(prop-2-enoylamino)propane-1-sulfonic acid;sodium Chemical compound [Na].OS(=O)(=O)CC(C)(C)NC(=O)C=C OPRIWFSSXKQMPB-UHFFFAOYSA-N 0.000 claims 1
- 239000000499 gel Substances 0.000 description 43
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 39
- 239000003921 oil Substances 0.000 description 35
- 239000000243 solution Substances 0.000 description 26
- 238000004519 manufacturing process Methods 0.000 description 16
- 238000000034 method Methods 0.000 description 16
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 15
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- 239000002253 acid Substances 0.000 description 11
- 239000011651 chromium Substances 0.000 description 11
- 239000012530 fluid Substances 0.000 description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- 239000011541 reaction mixture Substances 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 9
- 239000008367 deionised water Substances 0.000 description 9
- 229910021641 deionized water Inorganic materials 0.000 description 9
- 229920002401 polyacrylamide Polymers 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- HFBMWMNUJJDEQZ-UHFFFAOYSA-N acryloyl chloride Chemical compound ClC(=O)C=C HFBMWMNUJJDEQZ-UHFFFAOYSA-N 0.000 description 7
- 239000007864 aqueous solution Substances 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 7
- 238000005160 1H NMR spectroscopy Methods 0.000 description 6
- 238000000605 extraction Methods 0.000 description 6
- 238000002347 injection Methods 0.000 description 6
- 239000007924 injection Substances 0.000 description 6
- 238000004611 spectroscopical analysis Methods 0.000 description 6
- 239000008346 aqueous phase Substances 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- 238000005336 cracking Methods 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 229920002959 polymer blend Polymers 0.000 description 5
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 5
- 238000001556 precipitation Methods 0.000 description 5
- 239000011435 rock Substances 0.000 description 5
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 4
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- 229920001222 biopolymer Polymers 0.000 description 4
- 239000000872 buffer Substances 0.000 description 4
- PHFQLYPOURZARY-UHFFFAOYSA-N chromium trinitrate Chemical compound [Cr+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O PHFQLYPOURZARY-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- -1 Ca<2+>Mg<2+> Chemical class 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- BHELZAPQIKSEDF-UHFFFAOYSA-N allyl bromide Chemical compound BrCC=C BHELZAPQIKSEDF-UHFFFAOYSA-N 0.000 description 3
- 229910021538 borax Inorganic materials 0.000 description 3
- 230000003111 delayed effect Effects 0.000 description 3
- 238000001879 gelation Methods 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 235000010339 sodium tetraborate Nutrition 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 3
- OISVCGZHLKNMSJ-UHFFFAOYSA-N 2,6-dimethylpyridine Chemical compound CC1=CC=CC(C)=N1 OISVCGZHLKNMSJ-UHFFFAOYSA-N 0.000 description 2
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- FLZDRQXGVYVYSL-UHFFFAOYSA-N 3-(2-cyanopropyldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)CN=NCC(C)C#N FLZDRQXGVYVYSL-UHFFFAOYSA-N 0.000 description 2
- ASHGTJPOSUFTGB-UHFFFAOYSA-N 3-methoxyphenol Chemical compound COC1=CC=CC(O)=C1 ASHGTJPOSUFTGB-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- WDJHALXBUFZDSR-UHFFFAOYSA-N acetoacetic acid Chemical compound CC(=O)CC(O)=O WDJHALXBUFZDSR-UHFFFAOYSA-N 0.000 description 2
- 125000003368 amide group Chemical group 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 239000010779 crude oil Substances 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- 238000004949 mass spectrometry Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- GNVNKFUEUXUWDV-VIFPVBQESA-N (2s)-2-amino-3-[4-(aminomethyl)phenyl]propanoic acid Chemical compound NCC1=CC=C(C[C@H](N)C(O)=O)C=C1 GNVNKFUEUXUWDV-VIFPVBQESA-N 0.000 description 1
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
- DZSVIVLGBJKQAP-UHFFFAOYSA-N 1-(2-methyl-5-propan-2-ylcyclohex-2-en-1-yl)propan-1-one Chemical compound CCC(=O)C1CC(C(C)C)CC=C1C DZSVIVLGBJKQAP-UHFFFAOYSA-N 0.000 description 1
- LTMRRSWNXVJMBA-UHFFFAOYSA-L 2,2-diethylpropanedioate Chemical compound CCC(CC)(C([O-])=O)C([O-])=O LTMRRSWNXVJMBA-UHFFFAOYSA-L 0.000 description 1
- WYWWNVMODHTVQY-UHFFFAOYSA-N 2-(prop-2-enoylamino)propanedioic acid Chemical compound OC(=O)C(C(O)=O)NC(=O)C=C WYWWNVMODHTVQY-UHFFFAOYSA-N 0.000 description 1
- GRNHZMGFVFTJHF-UHFFFAOYSA-N 2-hydroxyacetic acid;prop-2-enamide Chemical compound NC(=O)C=C.OCC(O)=O GRNHZMGFVFTJHF-UHFFFAOYSA-N 0.000 description 1
- WGLQHUKCXBXUDV-UHFFFAOYSA-N 3-aminophthalic acid Chemical compound NC1=CC=CC(C(O)=O)=C1C(O)=O WGLQHUKCXBXUDV-UHFFFAOYSA-N 0.000 description 1
- WUBBRNOQWQTFEX-UHFFFAOYSA-N 4-aminosalicylic acid Chemical compound NC1=CC=C(C(O)=O)C(O)=C1 WUBBRNOQWQTFEX-UHFFFAOYSA-N 0.000 description 1
- SLBQXWXKPNIVSQ-UHFFFAOYSA-N 4-nitrophthalic acid Chemical compound OC(=O)C1=CC=C([N+]([O-])=O)C=C1C(O)=O SLBQXWXKPNIVSQ-UHFFFAOYSA-N 0.000 description 1
- ZDZVKPXKLLLOOA-UHFFFAOYSA-N Allylmalonic acid Chemical compound OC(=O)C(C(O)=O)CC=C ZDZVKPXKLLLOOA-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 244000007835 Cyamopsis tetragonoloba Species 0.000 description 1
- WLTCKEHCTUYJGI-UHFFFAOYSA-N Diethyl aminomalonate Chemical compound CCOC(=O)C(N)C(=O)OCC WLTCKEHCTUYJGI-UHFFFAOYSA-N 0.000 description 1
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 229960004909 aminosalicylic acid Drugs 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003729 cation exchange resin Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 229920001429 chelating resin Polymers 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- GDWAYKGILJJNBB-UHFFFAOYSA-N diethyl 2-prop-2-enylpropanedioate Chemical compound CCOC(=O)C(CC=C)C(=O)OCC GDWAYKGILJJNBB-UHFFFAOYSA-N 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- HPYNZHMRTTWQTB-UHFFFAOYSA-N dimethylpyridine Natural products CC1=CC=CN=C1C HPYNZHMRTTWQTB-UHFFFAOYSA-N 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 150000002466 imines Chemical class 0.000 description 1
- NBZBKCUXIYYUSX-UHFFFAOYSA-N iminodiacetic acid Chemical compound OC(=O)CNCC(O)=O NBZBKCUXIYYUSX-UHFFFAOYSA-N 0.000 description 1
- 238000010952 in-situ formation Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000011221 initial treatment Methods 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000010355 oscillation Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- MUMZUERVLWJKNR-UHFFFAOYSA-N oxoplatinum Chemical compound [Pt]=O MUMZUERVLWJKNR-UHFFFAOYSA-N 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229910003446 platinum oxide Inorganic materials 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 1
- 229940001584 sodium metabisulfite Drugs 0.000 description 1
- 235000010262 sodium metabisulphite Nutrition 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 235000010493 xanthan gum Nutrition 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
- C09K8/887—Compositions based on water or polar solvents containing organic compounds macromolecular compounds containing cross-linking agents
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
- C08K3/011—Crosslinking or vulcanising agents, e.g. accelerators
-
- 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
- C09K8/06—Clay-free compositions
- C09K8/12—Clay-free compositions containing synthetic organic macromolecular compounds or their precursors
-
- 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
- C09K8/50—Compositions for plastering borehole walls, i.e. compositions for temporary consolidation of borehole walls
- C09K8/504—Compositions based on water or polar solvents
- C09K8/506—Compositions based on water or polar solvents containing organic compounds
- C09K8/508—Compositions based on water or polar solvents containing organic compounds macromolecular compounds
- C09K8/512—Compositions based on water or polar solvents containing organic compounds macromolecular compounds containing cross-linking agents
-
- 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
- C09K8/685—Compositions based on water or polar solvents containing organic compounds containing cross-linking agents
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S507/00—Earth boring, well treating, and oil field chemistry
- Y10S507/902—Controlled release agent
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S507/00—Earth boring, well treating, and oil field chemistry
- Y10S507/903—Crosslinked resin or polymer
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S507/00—Earth boring, well treating, and oil field chemistry
- Y10S507/922—Fracture fluid
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S507/00—Earth boring, well treating, and oil field chemistry
- Y10S507/935—Enhanced oil recovery
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Colloid Chemistry (AREA)
- Fats And Perfumes (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT02217390A IT1243492B (it) | 1990-11-23 | 1990-11-23 | Composizioni acquose gelificabili contenenti polimeri con particolari gruppi funzionali chelanti utili per il recupero del petrolio da un giacimento. |
Publications (3)
Publication Number | Publication Date |
---|---|
NO914555D0 NO914555D0 (no) | 1991-11-21 |
NO914555L NO914555L (no) | 1992-05-25 |
NO303582B1 true NO303582B1 (no) | 1998-08-03 |
Family
ID=11192583
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO914555A NO303582B1 (no) | 1990-11-23 | 1991-11-21 | Geldannende vandige blandinger og anvendelse av blandingene ved utvinnelse av olje fra et oljefelt |
Country Status (10)
Country | Link |
---|---|
US (1) | US5256315A (fr) |
EP (1) | EP0487153B1 (fr) |
JP (1) | JPH04330932A (fr) |
BR (1) | BR9105087A (fr) |
CA (1) | CA2056074C (fr) |
DK (1) | DK0487153T3 (fr) |
ES (2) | ES2068492T3 (fr) |
IT (1) | IT1243492B (fr) |
MX (1) | MX173905B (fr) |
NO (1) | NO303582B1 (fr) |
Families Citing this family (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IT1237794B (it) * | 1989-12-21 | 1993-06-17 | Eniricerche Spa | Copolimeri acrilammidici contenenti unita' (met) acrilammido benzendicarbossiliche |
IT1238234B (it) * | 1989-12-21 | 1993-07-12 | Eniricerche Spa | Polimeri contenenti unita' (met) acrilammido maloniche |
DE4221863C2 (de) * | 1992-07-03 | 1997-04-17 | Stockhausen Chem Fab Gmbh | Copolymere der Allyliminodiessigsäure mit ungesättigten Carbonsäuren und deren Verwendung als Komplexbildner, Peroxidstabilisatoren, Builder in Wasch- und Reinigungsmitteln und Dispergatoren |
US5789350A (en) * | 1996-02-12 | 1998-08-04 | Phillips Petroleum Company | Compositions and processes for treating hydrocarbon-bearing formations |
US6166103A (en) * | 1998-12-21 | 2000-12-26 | Atlantic Richfield Company | Aqueous gelable compositions with delayed gelling times |
US6539427B1 (en) | 1999-06-29 | 2003-03-25 | Cisco Technology, Inc. | Dynamically adaptive network element in a feedback-based data network |
ITBO20000745A1 (it) * | 2000-12-27 | 2002-06-27 | Carmelo Protopapa | Procedimento per la reticolazione di un polimero o di un copolimero acrilico o acrilderivato e del relativo polimero acrilico ottenuto |
US20030027964A1 (en) * | 2001-01-29 | 2003-02-06 | Murat Quadir | High molecular weight polymers containing pendant salicylic acid groups |
US7138472B2 (en) * | 2001-01-29 | 2006-11-21 | Nalco Company | High molecular weight polymers containing pendant salicylic acid groups for clarifying bayer process liquors |
WO2002078454A1 (fr) * | 2001-03-29 | 2002-10-10 | Francisco Pujol Alcover | Procede de dosage et machine de dosage de pates alimentaires correspondante |
US6949491B2 (en) * | 2001-09-26 | 2005-09-27 | Cooke Jr Claude E | Method and materials for hydraulic fracturing of wells |
US7104327B2 (en) * | 2003-08-19 | 2006-09-12 | Halliburton Engery Services, Inc. | Methods of fracturing high temperature subterranean zones and foamed fracturing fluids therefor |
US7723099B2 (en) * | 2003-09-10 | 2010-05-25 | Abbott Point Of Care Inc. | Immunoassay device with immuno-reference electrode |
US7325615B2 (en) * | 2005-05-02 | 2008-02-05 | Halliburton Energy Services, Inc. | Viscosified treatment fluids comprising polycarboxylic acid gelling agents and associated methods |
US8129317B2 (en) * | 2005-05-02 | 2012-03-06 | Halliburton Energy Services, Inc. | Viscosified treatment fluids comprising polycarboxylic acid gelling agents and associated methods |
US7857078B2 (en) * | 2007-05-29 | 2010-12-28 | Baker Hughes Incorporated | Cutting tools and methods of making the same |
WO2013062891A2 (fr) | 2011-10-28 | 2013-05-02 | Dow Global Technologies Llc | Procédé de fabrication de cellules photovoltaïques à base de chalcogénure |
WO2014113206A1 (fr) | 2013-01-18 | 2014-07-24 | Conocophillips Company | Nanogels pour gélification retardée |
AU2015350513B2 (en) | 2014-11-19 | 2019-08-15 | Conocophillips Company | Delayed gelation of polymers |
JP6843859B2 (ja) * | 2015-12-02 | 2021-03-17 | サウジ アラビアン オイル カンパニー | 高温架橋された破砕流体 |
US11326092B2 (en) | 2020-08-24 | 2022-05-10 | Saudi Arabian Oil Company | High temperature cross-linked fracturing fluids with reduced friction |
US12025589B2 (en) | 2021-12-06 | 2024-07-02 | Saudi Arabian Oil Company | Indentation method to measure multiple rock properties |
US12012550B2 (en) | 2021-12-13 | 2024-06-18 | Saudi Arabian Oil Company | Attenuated acid formulations for acid stimulation |
CN115057964A (zh) * | 2022-07-11 | 2022-09-16 | 中国石油大学(华东) | 一种用于高温压裂液的交联剂的制备方法 |
CN116289204B (zh) * | 2023-04-12 | 2023-10-13 | 潮州市丹辉婚纱礼服有限公司 | 一种抗静电透湿涤纶面料的制备方法和应用 |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1411715A (fr) * | 1964-06-09 | 1965-09-24 | Nobel Bozel | Amides alpha, beta-éthyléniques nu-alcoylolées et leur procédé de fabrication |
FR1458364A (fr) * | 1965-08-26 | 1966-03-04 | Nobel Bozel | Nouvelles laques acryliques thermodurcissables |
US3331773A (en) * | 1966-07-22 | 1967-07-18 | Grace W R & Co | Process for inhibiting precipitation in water |
US4137182A (en) * | 1977-06-20 | 1979-01-30 | Standard Oil Company (Indiana) | Process for fracturing well formations using aqueous gels |
DE2965577D1 (en) * | 1978-09-21 | 1983-07-07 | Eastman Kodak Co | Photographic recording material containing polymers which coordinate with metal ions |
US4193796A (en) * | 1978-12-20 | 1980-03-18 | Eastman Kodak Company | Polymers for use in image receiving elements for metallizable dyes in image transfer film units |
DE2920377A1 (de) * | 1979-05-19 | 1980-12-04 | Basf Ag | Binde-, impraegnier- und ueberzugsmittel auf basis einer waessrigen dispersion eines amidgruppenhaltigen copolymerisats |
US4228257A (en) * | 1979-06-06 | 1980-10-14 | Eastman Kodak Company | Polymers for use in image receiving elements for metallizable dyes in image transfer film units |
US4360425A (en) * | 1981-09-14 | 1982-11-23 | American Cyanamid Company | Low molecular weight copolymers and terpolymers as depressants in mineral ore flotation |
US4610305A (en) * | 1983-06-02 | 1986-09-09 | The New Mexico Institute Of Mining And Technology | Oilfield flooding polymer |
US4649183A (en) * | 1985-06-12 | 1987-03-10 | University Of Southern Mississippi | Calcium-tolerant N-substituted acrylamides as thickeners for aqueous systems |
US4686456A (en) * | 1985-06-18 | 1987-08-11 | Kabushiki Kaisha Toshiba | Memory test circuit |
US4774283A (en) * | 1987-03-02 | 1988-09-27 | Air Products And Chemicals, Inc. | Nonwoven binders of vinyl acetate/ethylene/self-crosslinking monomers/acrylamide copolymers having improved blocking resistance |
JPH075680B2 (ja) * | 1987-07-03 | 1995-01-25 | 三井石油化学工業株式会社 | 硬化性組成物 |
US4844970A (en) * | 1988-01-12 | 1989-07-04 | Air Products And Chemicals, Inc. | Zirconium (III) salts as cure co-catalysts for nonwoven binders comprising acrylamidoglycolic acid |
IT1229217B (it) * | 1989-03-31 | 1991-07-26 | Eniricerche S P A Agip S P A | Composizione acquosa gelificabile e suo impiego nei procedimenti di recupero assistito del petrolio. |
-
1990
- 1990-11-23 IT IT02217390A patent/IT1243492B/it active IP Right Grant
-
1991
- 1991-11-16 ES ES91202985T patent/ES2068492T3/es not_active Expired - Lifetime
- 1991-11-16 EP EP91202985A patent/EP0487153B1/fr not_active Expired - Lifetime
- 1991-11-16 DK DK91202985.7T patent/DK0487153T3/da active
- 1991-11-18 US US07/793,524 patent/US5256315A/en not_active Expired - Lifetime
- 1991-11-21 NO NO914555A patent/NO303582B1/no unknown
- 1991-11-21 ES ES19919103497U patent/ES1019384Y/es not_active Expired - Fee Related
- 1991-11-22 MX MX9102188A patent/MX173905B/es unknown
- 1991-11-22 BR BR919105087A patent/BR9105087A/pt not_active IP Right Cessation
- 1991-11-22 CA CA002056074A patent/CA2056074C/fr not_active Expired - Fee Related
- 1991-11-22 JP JP3332924A patent/JPH04330932A/ja not_active Withdrawn
Also Published As
Publication number | Publication date |
---|---|
MX173905B (es) | 1994-04-07 |
ES2068492T3 (es) | 1995-04-16 |
NO914555L (no) | 1992-05-25 |
DK0487153T3 (da) | 1995-05-01 |
NO914555D0 (no) | 1991-11-21 |
EP0487153B1 (fr) | 1995-01-11 |
CA2056074C (fr) | 2002-07-23 |
CA2056074A1 (fr) | 1992-05-24 |
US5256315A (en) | 1993-10-26 |
IT1243492B (it) | 1994-06-15 |
IT9022173A1 (it) | 1992-05-23 |
ES1019384U (es) | 1992-03-16 |
IT9022173A0 (it) | 1990-11-23 |
JPH04330932A (ja) | 1992-11-18 |
ES1019384Y (es) | 1992-11-01 |
EP0487153A1 (fr) | 1992-05-27 |
BR9105087A (pt) | 1992-06-23 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
NO303582B1 (no) | Geldannende vandige blandinger og anvendelse av blandingene ved utvinnelse av olje fra et oljefelt | |
CN103160268B (zh) | 一种纳米二氧化硅/聚合物驱油剂及其合成方法 | |
US6277900B1 (en) | Well cementing aids | |
US4709759A (en) | Enhanced oil recovery with hydrophobically associating polymers containing N-vinyl-pyrrolidone functionality | |
CN107759738B (zh) | 一种水溶性热增黏共聚物、制备方法及应用 | |
CN104927828A (zh) | 耐高温有机锆交联剂及其制备方法以及一种压裂液冻胶及其制备方法 | |
NO328619B1 (no) | Fremgangsmate for a redusere vannproduksjonen i en hydrokarbonbronn | |
CN104388063B (zh) | 一种钻井液用微交联聚合物类降滤失剂及其制备方法 | |
CN103665260A (zh) | 一种耐温抗盐驱油用聚合物及其制备方法 | |
CN108117621B (zh) | 一种增粘型抗钙盐聚合物降滤失剂及制备方法 | |
US4626285A (en) | Fluid loss control in oil field cements | |
CN114989348A (zh) | 一种抗高温抗盐有机硅降滤失剂及其制备方法与应用 | |
CA3015984C (fr) | Monomere d'acide maleamique et methode de preparation associee, copolymere aleatoire, methode de preparation et utilisation associee, et fluide de forage | |
US4502966A (en) | Terpolymers for use as high temperature fluid loss additive and rheology stabilizer for high pressure, high temperature oil well drilling fluids | |
CN108949124A (zh) | 一种成胶聚合物及其制备方法、聚合物弱凝胶钻井液 | |
US4931194A (en) | Enhanced oil recovery with high molecular weight polyvinylamine formed in-situ | |
CN102559156B (zh) | 一种钻井液用高温高盐降滤失剂及其制备方法 | |
CN111139039B (zh) | 一种磺化酚醛树脂接枝改性聚合物降滤失剂及其制备方法 | |
CN106478463B (zh) | 一种耐温抗盐单体和聚合物及其制备方法和应用 | |
CN107759729B (zh) | 一种钻井液用耐温耐盐增黏剂、制备方法及应用 | |
CN103409125B (zh) | 一种水溶性四元共聚物驱油剂及其合成方法 | |
CN104327278A (zh) | 一种含壳聚糖的疏水缔合聚合物驱油剂及其制备方法 | |
US4683952A (en) | Fluid loss control in oil field cements | |
CN102633938B (zh) | 一种AM/BAMACB[7]/AMPS-Na共聚物及制备方法 | |
CN103320113B (zh) | 一种水溶性am-aa-nvp-bema四元共聚物驱油剂及其合成方法 |