NO302841B1 - Vandig geldannende blanding og en fremgangsmåte for å redusere permeabiliteten i et petroleumsreservoar - Google Patents

Vandig geldannende blanding og en fremgangsmåte for å redusere permeabiliteten i et petroleumsreservoar Download PDF

Info

Publication number: NO302841B1
Authority: NO; Norway
Prior art keywords: acid; mixture; alpha; range; ligand
Prior art date: 1991-03-28

Application number

NO921053A

Other languages

English (en)

Norwegian (no)

Other versions

NO921053D0 (no

NO921053L (no

Inventor

Thomas Paul Lockhart

Paola Albonico

Original Assignee

Eniricerche Spa

Agip Spa

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1991-03-28

Filing date

1992-03-18

Publication date

1998-04-27

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=11359325&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=NO302841(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1992-03-18 Application filed by Eniricerche Spa, Agip Spa filed Critical Eniricerche Spa

1992-03-18 Publication of NO921053D0 publication Critical patent/NO921053D0/no

1992-09-29 Publication of NO921053L publication Critical patent/NO921053L/no

1998-04-27 Publication of NO302841B1 publication Critical patent/NO302841B1/no

Links

239000000203 mixture Substances 0.000 title claims description 88
230000035699 permeability Effects 0.000 title claims description 21
239000003208 petroleum Substances 0.000 title claims description 19
238000000034 method Methods 0.000 title claims description 12
239000011651 chromium Substances 0.000 claims description 67
239000003446 ligand Substances 0.000 claims description 45
YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims description 36
238000001879 gelation Methods 0.000 claims description 35
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 34
UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims description 32
CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 30
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 27
VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 26
229910052804 chromium Inorganic materials 0.000 claims description 26
238000004132 cross linking Methods 0.000 claims description 24
229920001577 copolymer Polymers 0.000 claims description 23
AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 claims description 22
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims description 18
229960004889 salicylic acid Drugs 0.000 claims description 18
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 16
235000010323 ascorbic acid Nutrition 0.000 claims description 15
239000011668 ascorbic acid Substances 0.000 claims description 15
229910001430 chromium ion Inorganic materials 0.000 claims description 14
229960005070 ascorbic acid Drugs 0.000 claims description 13
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 12
OFOBLEOULBTSOW-UHFFFAOYSA-L Malonate Chemical compound [O-]C(=O)CC([O-])=O OFOBLEOULBTSOW-UHFFFAOYSA-L 0.000 claims description 10
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 8
125000001931 aliphatic group Chemical group 0.000 claims description 8
125000000217 alkyl group Chemical group 0.000 claims description 8
229920000642 polymer Polymers 0.000 claims description 8
230000000979 retarding effect Effects 0.000 claims description 8
MTCFGRXMJLQNBG-UHFFFAOYSA-N serine Chemical compound OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 claims description 8
MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 claims description 7
AFENDNXGAFYKQO-UHFFFAOYSA-N 2-hydroxybutyric acid Chemical compound CCC(O)C(O)=O AFENDNXGAFYKQO-UHFFFAOYSA-N 0.000 claims description 7
229920006322 acrylamide copolymer Polymers 0.000 claims description 7
-1 aliphatic alpha-hydroxy acids Chemical class 0.000 claims description 7
230000003111 delayed effect Effects 0.000 claims description 7
JFCQEDHGNNZCLN-UHFFFAOYSA-N glutaric acid Chemical compound OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 claims description 7
229920002401 polyacrylamide Polymers 0.000 claims description 7
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 description 7
QWCKQJZIFLGMSD-UHFFFAOYSA-N 2-Aminobutanoic acid Natural products CCC(N)C(O)=O QWCKQJZIFLGMSD-UHFFFAOYSA-N 0.000 claims description 6
AEMRFAOFKBGASW-UHFFFAOYSA-M Glycolate Chemical compound OCC([O-])=O AEMRFAOFKBGASW-UHFFFAOYSA-M 0.000 claims description 6
WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 6
125000003368 amide group Chemical group 0.000 claims description 6
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 6
229920000620 organic polymer Polymers 0.000 claims description 6
RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 claims description 5
DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims description 5
229940061720 alpha hydroxy acid Drugs 0.000 claims description 5
239000013110 organic ligand Substances 0.000 claims description 5
150000003839 salts Chemical class 0.000 claims description 5
239000003381 stabilizer Substances 0.000 claims description 5
QWCKQJZIFLGMSD-GSVOUGTGSA-N D-alpha-aminobutyric acid Chemical compound CC[C@@H](N)C(O)=O QWCKQJZIFLGMSD-GSVOUGTGSA-N 0.000 claims description 4
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 4
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 4
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 4
125000003118 aryl group Chemical group 0.000 claims description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
125000002768 hydroxyalkyl group Chemical group 0.000 claims description 4
150000002596 lactones Chemical class 0.000 claims description 4
239000004471 Glycine Substances 0.000 claims description 3
235000008206 alpha-amino acids Nutrition 0.000 claims description 3
239000004310 lactic acid Substances 0.000 claims description 3
235000014655 lactic acid Nutrition 0.000 claims description 3
239000011734 sodium Substances 0.000 claims description 3
229920003169 water-soluble polymer Polymers 0.000 claims description 3
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 2
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 2
FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 claims description 2
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 claims description 2
JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 claims description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims description 2
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 2
FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims description 2
239000002253 acid Substances 0.000 claims description 2
150000007513 acids Chemical class 0.000 claims description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 claims description 2
239000001361 adipic acid Substances 0.000 claims description 2
235000011037 adipic acid Nutrition 0.000 claims description 2
QWCKQJZIFLGMSD-UHFFFAOYSA-M alpha-aminobutyrate Chemical compound CCC(N)C([O-])=O QWCKQJZIFLGMSD-UHFFFAOYSA-M 0.000 claims description 2
150000001412 amines Chemical class 0.000 claims description 2
229940072107 ascorbate Drugs 0.000 claims description 2
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 claims description 2
239000013505 freshwater Substances 0.000 claims description 2
125000004356 hydroxy functional group Chemical group O* 0.000 claims description 2
229910001410 inorganic ion Inorganic materials 0.000 claims description 2
FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims description 2
239000000178 monomer Substances 0.000 claims description 2
230000007935 neutral effect Effects 0.000 claims description 2
XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 claims description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 2
KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 claims description 2
235000002906 tartaric acid Nutrition 0.000 claims description 2
239000011975 tartaric acid Substances 0.000 claims description 2
229940095064 tartrate Drugs 0.000 claims description 2
229920001897 terpolymer Polymers 0.000 claims description 2
CYMRPDYINXWJFU-UHFFFAOYSA-N 2-carbamoylbenzoic acid Chemical compound NC(=O)C1=CC=CC=C1C(O)=O CYMRPDYINXWJFU-UHFFFAOYSA-N 0.000 claims 1
238000010668 complexation reaction Methods 0.000 claims 1
GICLSALZHXCILJ-UHFFFAOYSA-N ctk5a5089 Chemical compound NCC(O)=O.NCC(O)=O GICLSALZHXCILJ-UHFFFAOYSA-N 0.000 claims 1
150000002500 ions Chemical class 0.000 claims 1
YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 claims 1
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 15
239000007864 aqueous solution Substances 0.000 description 10
239000000499 gel Substances 0.000 description 10
229960004275 glycolic acid Drugs 0.000 description 8
239000000243 solution Substances 0.000 description 8
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
230000015572 biosynthetic process Effects 0.000 description 5
238000000605 extraction Methods 0.000 description 5
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
238000010586 diagram Methods 0.000 description 4
238000002474 experimental method Methods 0.000 description 4
229960001153 serine Drugs 0.000 description 4
WYYQVWLEPYFFLP-UHFFFAOYSA-K chromium(3+);triacetate Chemical compound [Cr+3].CC([O-])=O.CC([O-])=O.CC([O-])=O WYYQVWLEPYFFLP-UHFFFAOYSA-K 0.000 description 3
239000012530 fluid Substances 0.000 description 3
229910021645 metal ion Inorganic materials 0.000 description 3
238000003786 synthesis reaction Methods 0.000 description 3
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
230000032683 aging Effects 0.000 description 2
239000002585 base Substances 0.000 description 2
238000002347 injection Methods 0.000 description 2
239000007924 injection Substances 0.000 description 2
150000007522 mineralic acids Chemical class 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
239000003340 retarding agent Substances 0.000 description 2
239000013535 sea water Substances 0.000 description 2
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 description 1
239000003513 alkali Substances 0.000 description 1
150000001280 alpha hydroxy acids Chemical class 0.000 description 1
150000001371 alpha-amino acids Chemical class 0.000 description 1
230000033228 biological regulation Effects 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
150000007942 carboxylates Chemical class 0.000 description 1
230000021523 carboxylation Effects 0.000 description 1
238000006473 carboxylation reaction Methods 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
BFGKITSFLPAWGI-UHFFFAOYSA-N chromium(3+) Chemical compound [Cr+3] BFGKITSFLPAWGI-UHFFFAOYSA-N 0.000 description 1
230000009918 complex formation Effects 0.000 description 1
239000003431 cross linking reagent Substances 0.000 description 1
230000001934 delay Effects 0.000 description 1
239000007789 gas Substances 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
150000007529 inorganic bases Chemical class 0.000 description 1
150000002690 malonic acid derivatives Chemical class 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
230000002028 premature Effects 0.000 description 1
239000011435 rock Substances 0.000 description 1
239000003352 sequestering agent Substances 0.000 description 1
229910052708 sodium Inorganic materials 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
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F11/00—Compounds containing elements of Groups 6 or 16 of the Periodic Table
- C07F11/005—Compounds containing elements of Groups 6 or 16 of the Periodic Table compounds without a metal-carbon linkage
- 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
- 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)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
General Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Compositions Of Macromolecular Compounds (AREA)
Cosmetics (AREA)
Medicinal Preparation (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Consolidation Of Soil By Introduction Of Solidifying Substances Into Soil (AREA)
Colloid Chemistry (AREA)
Physical Or Chemical Processes And Apparatus (AREA)
Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)

NO921053A 1991-03-28 1992-03-18 Vandig geldannende blanding og en fremgangsmåte for å redusere permeabiliteten i et petroleumsreservoar NO302841B1 (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
ITMI910858A IT1245383B (it)	1991-03-28	1991-03-28	Composizione acquosa gelificabile avente tempo di gelificazione ritardato

Publications (3)

Publication Number	Publication Date
NO921053D0 NO921053D0 (no)	1992-03-18
NO921053L NO921053L (no)	1992-09-29
NO302841B1 true NO302841B1 (no)	1998-04-27

Family

ID=11359325

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO921053A NO302841B1 (no)	1991-03-28	1992-03-18	Vandig geldannende blanding og en fremgangsmåte for å redusere permeabiliteten i et petroleumsreservoar

Country Status (10)

Country	Link
US (1)	US5338465A (fr)
EP (1)	EP0506191B2 (fr)
JP (1)	JPH05125354A (fr)
BR (1)	BR9201086A (fr)
CA (1)	CA2063877C (fr)
DK (1)	DK0506191T4 (fr)
ES (1)	ES2081553T5 (fr)
IT (1)	IT1245383B (fr)
MX (1)	MX9201404A (fr)
NO (1)	NO302841B1 (fr)

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* Cited by examiner, † Cited by third party
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US5421411A (en) *	1994-01-03	1995-06-06	Marathon Oil Company	Process for reducing permeability in a subterranean hydrocarbon-bearing formation utilizing a gelation solution having a controlled gelation rate
US5415229A (en) *	1994-01-03	1995-05-16	Marathon Oil Company	Hydrocarbon recovery process utilizing a gel prepared from a polymer and a preformed crosslinking agent
US5431226A (en) *	1994-01-03	1995-07-11	Marathan Oil Company	Process for reducing permeability in a high-temperature subterranean hydrocarbon-bearing formation utilizing a decarboxylated crosslinking agent
YU58599A (sh) *	1997-05-16	2000-12-28	Amgen Inc.	Gelovi sa usporenim podržanim oslobađanjem
US6152234A (en) *	1998-06-10	2000-11-28	Atlantic Richfield Company	Method for strengthening a subterranean formation
US6189615B1 (en)	1998-12-15	2001-02-20	Marathon Oil Company	Application of a stabilized polymer gel to an alkaline treatment region for improved hydrocarbon recovery
US6166103A (en) *	1998-12-21	2000-12-26	Atlantic Richfield Company	Aqueous gelable compositions with delayed gelling times
US6156819A (en) *	1998-12-21	2000-12-05	Atlantic Richfield Company	Use of low- and high-molecular-weight polymers in well treatments
US6133204A (en) *	1999-02-09	2000-10-17	Atlantic Richfield Company	Use of oil-based gel-breaker/inhibitor compounds with polymer gels in well treatments
US6265355B1 (en)	1999-02-09	2001-07-24	Atlantic Richfield Company	Gel-breaker composition and a method for breaking a gel
US7281579B2 (en) *	2001-12-07	2007-10-16	Aqueolic Canada Ltd.	Method for terminating or reducing water flow in a subterranean formation
US7216711B2 (en)	2002-01-08	2007-05-15	Halliburton Eenrgy Services, Inc.	Methods of coating resin and blending resin-coated proppant
US7343973B2 (en)	2002-01-08	2008-03-18	Halliburton Energy Services, Inc.	Methods of stabilizing surfaces of subterranean formations
US7267171B2 (en)	2002-01-08	2007-09-11	Halliburton Energy Services, Inc.	Methods and compositions for stabilizing the surface of a subterranean formation
US6691780B2 (en)	2002-04-18	2004-02-17	Halliburton Energy Services, Inc.	Tracking of particulate flowback in subterranean wells
US20040211561A1 (en)	2003-03-06	2004-10-28	Nguyen Philip D.	Methods and compositions for consolidating proppant in fractures
US7114570B2 (en)	2003-04-07	2006-10-03	Halliburton Energy Services, Inc.	Methods and compositions for stabilizing unconsolidated subterranean formations
US6978836B2 (en)	2003-05-23	2005-12-27	Halliburton Energy Services, Inc.	Methods for controlling water and particulate production
US7413010B2 (en)	2003-06-23	2008-08-19	Halliburton Energy Services, Inc.	Remediation of subterranean formations using vibrational waves and consolidating agents
US7114560B2 (en)	2003-06-23	2006-10-03	Halliburton Energy Services, Inc.	Methods for enhancing treatment fluid placement in a subterranean formation
US7013976B2 (en)	2003-06-25	2006-03-21	Halliburton Energy Services, Inc.	Compositions and methods for consolidating unconsolidated subterranean formations
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1991
- 1991-03-28 IT ITMI910858A patent/IT1245383B/it active IP Right Grant
1992
- 1992-03-18 NO NO921053A patent/NO302841B1/no unknown
- 1992-03-19 US US07/853,839 patent/US5338465A/en not_active Expired - Lifetime
- 1992-03-21 EP EP92200820A patent/EP0506191B2/fr not_active Expired - Lifetime
- 1992-03-21 ES ES92200820T patent/ES2081553T5/es not_active Expired - Lifetime
- 1992-03-21 DK DK92200820T patent/DK0506191T4/da active
- 1992-03-24 CA CA002063877A patent/CA2063877C/fr not_active Expired - Fee Related
- 1992-03-27 BR BR929201086A patent/BR9201086A/pt not_active IP Right Cessation
- 1992-03-27 JP JP4100188A patent/JPH05125354A/ja not_active Withdrawn
- 1992-03-27 MX MX9201404A patent/MX9201404A/es not_active IP Right Cessation

Also Published As

Publication number	Publication date
MX9201404A (es)	1992-09-01
BR9201086A (pt)	1992-11-24
EP0506191A1 (fr)	1992-09-30
IT1245383B (it)	1994-09-20
EP0506191B1 (fr)	1995-12-13
DK0506191T3 (da)	1996-03-04
EP0506191B2 (fr)	1998-08-12
ES2081553T3 (es)	1996-03-16
ITMI910858A0 (it)	1991-03-28
NO921053D0 (no)	1992-03-18
CA2063877A1 (fr)	1992-09-29
DK0506191T4 (da)	1999-05-17
CA2063877C (fr)	2003-05-13
US5338465A (en)	1994-08-16
NO921053L (no)	1992-09-29
JPH05125354A (ja)	1993-05-21
ITMI910858A1 (it)	1992-09-28
ES2081553T5 (es)	1999-02-16

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