CA1201282A - Compositions liquides pour le conditionnement des puits - Google Patents

Compositions liquides pour le conditionnement des puits

Info

Publication number: CA1201282A
Authority: CA; Canada
Prior art keywords: composition; iodide; bromide; alkyl; chloride
Prior art date: 1981-12-31
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

Application number

CA000416810A

Other languages

English (en)

Inventor

Michael L. Walker

Joseph W. Johnson, Jr.

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Halliburton Co

Original Assignee

Halliburton Co

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

1981-12-31

Filing date

1982-12-01

Publication date

1986-03-04

1982-12-01 Application filed by Halliburton Co filed Critical Halliburton Co

1986-03-04 Application granted granted Critical

1986-03-04 Publication of CA1201282A publication Critical patent/CA1201282A/fr

Status Expired legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 113
239000012530 fluid Substances 0.000 title claims description 25
238000000034 method Methods 0.000 claims abstract description 21
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 20
-1 halogen salts Chemical class 0.000 claims abstract description 18
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 10
230000002706 hydrostatic effect Effects 0.000 claims abstract description 5
150000001412 amines Chemical class 0.000 claims description 27
VNDYJBBGRKZCSX-UHFFFAOYSA-L zinc bromide Chemical compound Br[Zn]Br VNDYJBBGRKZCSX-UHFFFAOYSA-L 0.000 claims description 25
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 24
150000003839 salts Chemical class 0.000 claims description 22
JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 claims description 22
230000007797 corrosion Effects 0.000 claims description 20
238000005260 corrosion Methods 0.000 claims description 20
239000002253 acid Substances 0.000 claims description 18
FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 claims description 18
NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 claims description 16
JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 claims description 16
UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 claims description 15
229910001622 calcium bromide Inorganic materials 0.000 claims description 15
239000001110 calcium chloride Substances 0.000 claims description 15
235000011148 calcium chloride Nutrition 0.000 claims description 15
229910001628 calcium chloride Inorganic materials 0.000 claims description 15
WGEFECGEFUFIQW-UHFFFAOYSA-L calcium dibromide Chemical compound [Ca+2].[Br-].[Br-] WGEFECGEFUFIQW-UHFFFAOYSA-L 0.000 claims description 15
TVDSBUOJIPERQY-UHFFFAOYSA-N prop-2-yn-1-ol Chemical compound OCC#C TVDSBUOJIPERQY-UHFFFAOYSA-N 0.000 claims description 15
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 14
150000003248 quinolines Chemical class 0.000 claims description 14
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 12
VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 claims description 12
IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 claims description 12
UAYWVJHJZHQCIE-UHFFFAOYSA-L zinc iodide Chemical compound I[Zn]I UAYWVJHJZHQCIE-UHFFFAOYSA-L 0.000 claims description 12
229940102001 zinc bromide Drugs 0.000 claims description 11
239000011592 zinc chloride Substances 0.000 claims description 11
235000005074 zinc chloride Nutrition 0.000 claims description 11
CUUQUEAUUPYEKK-UHFFFAOYSA-N 4-ethyloct-1-yn-3-ol Chemical compound CCCCC(CC)C(O)C#C CUUQUEAUUPYEKK-UHFFFAOYSA-N 0.000 claims description 10
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims description 10
WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 10
229940111121 antirheumatic drug quinolines Drugs 0.000 claims description 10
125000004432 carbon atom Chemical group C* 0.000 claims description 10
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims description 10
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 10
125000000217 alkyl group Chemical group 0.000 claims description 9
AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 claims description 8
150000003222 pyridines Chemical class 0.000 claims description 8
239000011780 sodium chloride Substances 0.000 claims description 7
JQZGUQIEPRIDMR-UHFFFAOYSA-N 3-methylbut-1-yn-1-ol Chemical compound CC(C)C#CO JQZGUQIEPRIDMR-UHFFFAOYSA-N 0.000 claims description 6
UNMYWSMUMWPJLR-UHFFFAOYSA-L Calcium iodide Chemical compound [Ca+2].[I-].[I-] UNMYWSMUMWPJLR-UHFFFAOYSA-L 0.000 claims description 6
CECABOMBVQNBEC-UHFFFAOYSA-K aluminium iodide Chemical compound I[Al](I)I CECABOMBVQNBEC-UHFFFAOYSA-K 0.000 claims description 6
SWLVFNYSXGMGBS-UHFFFAOYSA-N ammonium bromide Chemical compound [NH4+].[Br-] SWLVFNYSXGMGBS-UHFFFAOYSA-N 0.000 claims description 6
230000015572 biosynthetic process Effects 0.000 claims description 6
229910001640 calcium iodide Inorganic materials 0.000 claims description 6
235000009518 sodium iodide Nutrition 0.000 claims description 6
XZXYQEHISUMZAT-UHFFFAOYSA-N 2-[(2-hydroxy-5-methylphenyl)methyl]-4-methylphenol Chemical compound CC1=CC=C(O)C(CC=2C(=CC=C(C)C=2)O)=C1 XZXYQEHISUMZAT-UHFFFAOYSA-N 0.000 claims description 5
CEBKHWWANWSNTI-UHFFFAOYSA-N 2-methylbut-3-yn-2-ol Chemical compound CC(C)(O)C#C CEBKHWWANWSNTI-UHFFFAOYSA-N 0.000 claims description 5
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims description 5
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 5
150000001298 alcohols Chemical class 0.000 claims description 5
229940077484 ammonium bromide Drugs 0.000 claims description 5
229960001040 ammonium chloride Drugs 0.000 claims description 5
235000019270 ammonium chloride Nutrition 0.000 claims description 5
229940107816 ammonium iodide Drugs 0.000 claims description 5
229940046413 calcium iodide Drugs 0.000 claims description 5
150000001875 compounds Chemical class 0.000 claims description 5
235000019253 formic acid Nutrition 0.000 claims description 5
QXLPXWSKPNOQLE-UHFFFAOYSA-N methylpentynol Chemical compound CCC(C)(O)C#C QXLPXWSKPNOQLE-UHFFFAOYSA-N 0.000 claims description 5
229960002238 methylpentynol Drugs 0.000 claims description 5
239000001103 potassium chloride Substances 0.000 claims description 5
235000011164 potassium chloride Nutrition 0.000 claims description 5
235000007715 potassium iodide Nutrition 0.000 claims description 5
229960004839 potassium iodide Drugs 0.000 claims description 5
PUGUQINMNYINPK-UHFFFAOYSA-N tert-butyl 4-(2-chloroacetyl)piperazine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCN(C(=O)CCl)CC1 PUGUQINMNYINPK-UHFFFAOYSA-N 0.000 claims description 5
125000005270 trialkylamine group Chemical group 0.000 claims description 5
QYLFHLNFIHBCPR-UHFFFAOYSA-N 1-ethynylcyclohexan-1-ol Chemical compound C#CC1(O)CCCCC1 QYLFHLNFIHBCPR-UHFFFAOYSA-N 0.000 claims description 4
VQUXVWMAXIQKTQ-UHFFFAOYSA-N 3-methylnon-1-yn-3-ol Chemical compound CCCCCCC(C)(O)C#C VQUXVWMAXIQKTQ-UHFFFAOYSA-N 0.000 claims description 4
XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical compound CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 4
GKPOMITUDGXOSB-UHFFFAOYSA-N but-3-yn-2-ol Chemical compound CC(O)C#C GKPOMITUDGXOSB-UHFFFAOYSA-N 0.000 claims description 4
229940059251 calcium bromide Drugs 0.000 claims description 4
DQBUGZRLSSLUKC-UHFFFAOYSA-N dec-1-yn-3-ol Chemical compound CCCCCCCC(O)C#C DQBUGZRLSSLUKC-UHFFFAOYSA-N 0.000 claims description 4
230000002401 inhibitory effect Effects 0.000 claims description 4
VUGRNZHKYVHZSN-UHFFFAOYSA-N oct-1-yn-3-ol Chemical compound CCCCCC(O)C#C VUGRNZHKYVHZSN-UHFFFAOYSA-N 0.000 claims description 4
LBSKEFWQPNVWTP-UHFFFAOYSA-N pent-1-yn-3-ol Chemical compound CCC(O)C#C LBSKEFWQPNVWTP-UHFFFAOYSA-N 0.000 claims description 4
229940094035 potassium bromide Drugs 0.000 claims description 4
229960002816 potassium chloride Drugs 0.000 claims description 4
229940075581 sodium bromide Drugs 0.000 claims description 4
229960002668 sodium chloride Drugs 0.000 claims description 4
229940083599 sodium iodide Drugs 0.000 claims description 4
229960001939 zinc chloride Drugs 0.000 claims description 4
SHSFXAVQBIEYMK-UHFFFAOYSA-N hept-1-yn-3-ol Chemical compound CCCCC(O)C#C SHSFXAVQBIEYMK-UHFFFAOYSA-N 0.000 claims description 3
GJMTYVRMTSLDDV-UHFFFAOYSA-N but-3-yne-1,2-diol Chemical compound OCC(O)C#C GJMTYVRMTSLDDV-UHFFFAOYSA-N 0.000 claims description 2
229960002713 calcium chloride Drugs 0.000 claims 6
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 claims 4
KDKYADYSIPSCCQ-UHFFFAOYSA-N but-1-yne Chemical compound CCC#C KDKYADYSIPSCCQ-UHFFFAOYSA-N 0.000 claims 4
XGDWHBVKCBAJSM-UHFFFAOYSA-N 1-(2,4,6-trimethylcyclohex-3-en-1-yl)prop-2-yn-1-ol Chemical compound CC1CC(C)=CC(C)C1C(O)C#C XGDWHBVKCBAJSM-UHFFFAOYSA-N 0.000 claims 2
208000036366 Sensation of pressure Diseases 0.000 claims 1
PNNVOERUDIWYCP-UHFFFAOYSA-N hept-1-yn-1-ol Chemical compound CCCCCC#CO PNNVOERUDIWYCP-UHFFFAOYSA-N 0.000 claims 1
229910052742 iron Inorganic materials 0.000 claims 1
230000000149 penetrating effect Effects 0.000 claims 1
239000004615 ingredient Substances 0.000 abstract description 2
229910052736 halogen Inorganic materials 0.000 abstract 1
CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 7
SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 7
239000003112 inhibitor Substances 0.000 description 7
229910052751 metal Inorganic materials 0.000 description 7
239000002184 metal Substances 0.000 description 7
238000005755 formation reaction Methods 0.000 description 5
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 4
SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 4
239000003921 oil Substances 0.000 description 4
239000000126 substance Substances 0.000 description 4
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 3
229910000831 Steel Inorganic materials 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 3
239000003208 petroleum Substances 0.000 description 3
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
239000010959 steel Substances 0.000 description 3
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
239000008186 active pharmaceutical agent Substances 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
125000004122 cyclic group Chemical group 0.000 description 2
238000005553 drilling Methods 0.000 description 2
238000012986 modification Methods 0.000 description 2
230000004048 modification Effects 0.000 description 2
230000009972 noncorrosive effect Effects 0.000 description 2
WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
239000000243 solution Substances 0.000 description 2
CCFGTKQIRWHYTB-UHFFFAOYSA-N 2-methyl-3-nitropyridine Chemical compound CC1=NC=CC=C1[N+]([O-])=O CCFGTKQIRWHYTB-UHFFFAOYSA-N 0.000 description 1
125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
108091006629 SLC13A2 Proteins 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
JVVXZOOGOGPDRZ-SLFFLAALSA-N [(1R,4aS,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl]methanamine Chemical compound NC[C@]1(C)CCC[C@]2(C)C3=CC=C(C(C)C)C=C3CC[C@H]21 JVVXZOOGOGPDRZ-SLFFLAALSA-N 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
230000001154 acute effect Effects 0.000 description 1
PQLAYKMGZDUDLQ-UHFFFAOYSA-K aluminium bromide Chemical compound Br[Al](Br)Br PQLAYKMGZDUDLQ-UHFFFAOYSA-K 0.000 description 1
UKFWSNCTAHXBQN-UHFFFAOYSA-N ammonium iodide Chemical compound [NH4+].[I-] UKFWSNCTAHXBQN-UHFFFAOYSA-N 0.000 description 1
230000000740 bleeding effect Effects 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
238000011109 contamination Methods 0.000 description 1
239000010779 crude oil Substances 0.000 description 1
230000002939 deleterious effect Effects 0.000 description 1
HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 description 1
230000005484 gravity Effects 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
208000020442 loss of weight Diseases 0.000 description 1
SMUQFGGVLNAIOZ-UHFFFAOYSA-N methylquinoline Natural products C1=CC=CC2=NC(C)=CC=C21 SMUQFGGVLNAIOZ-UHFFFAOYSA-N 0.000 description 1
DIAIBWNEUYXDNL-UHFFFAOYSA-N n,n-dihexylhexan-1-amine Chemical compound CCCCCCN(CCCCCC)CCCCCC DIAIBWNEUYXDNL-UHFFFAOYSA-N 0.000 description 1
OOHAUGDGCWURIT-UHFFFAOYSA-N n,n-dipentylpentan-1-amine Chemical compound CCCCCN(CCCCC)CCCCC OOHAUGDGCWURIT-UHFFFAOYSA-N 0.000 description 1
SHMGVQVSZPVFOT-UHFFFAOYSA-N n-(5-cyclohexyl-2-methoxyphenyl)-4-methyl-3-(3-quinolin-4-ylpyridin-2-yl)oxybenzamide Chemical group C1=C(NC(=O)C=2C=C(OC=3C(=CC=CN=3)C=3C4=CC=CC=C4N=CC=3)C(C)=CC=2)C(OC)=CC=C1C1CCCCC1 SHMGVQVSZPVFOT-UHFFFAOYSA-N 0.000 description 1
JACMPVXHEARCBO-UHFFFAOYSA-N n-pentylpentan-1-amine Chemical compound CCCCCNCCCCC JACMPVXHEARCBO-UHFFFAOYSA-N 0.000 description 1
239000003129 oil well Substances 0.000 description 1
238000012856 packing Methods 0.000 description 1
UKIUSKWWNRYHOO-UHFFFAOYSA-N pent-1-yn-1-ol Chemical compound CCCC#CO UKIUSKWWNRYHOO-UHFFFAOYSA-N 0.000 description 1
DPBLXKKOBLCELK-UHFFFAOYSA-N pentan-1-amine Chemical compound CCCCCN DPBLXKKOBLCELK-UHFFFAOYSA-N 0.000 description 1
238000004391 petroleum recovery Methods 0.000 description 1
125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 1
238000011084 recovery Methods 0.000 description 1
239000012266 salt solution Substances 0.000 description 1
YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
229940086542 triethylamine Drugs 0.000 description 1
YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc 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
- C09K8/02—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
- 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
- C09K8/54—Compositions for in situ inhibition of corrosion in boreholes or wells

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)
Dispersion Chemistry (AREA)
Preventing Corrosion Or Incrustation Of Metals (AREA)

CA000416810A 1981-12-31 1982-12-01 Compositions liquides pour le conditionnement des puits Expired CA1201282A (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US33622081A	1981-12-31	1981-12-31
US336,220		1981-12-31

Publications (1)

Publication Number	Publication Date
CA1201282A true CA1201282A (fr)	1986-03-04

Family

ID=23315093

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000416810A Expired CA1201282A (fr)	1981-12-31	1982-12-01	Compositions liquides pour le conditionnement des puits

Country Status (4)

Country	Link
CA (1)	CA1201282A (fr)
DE (1)	DE3247872A1 (fr)
GB (1)	GB2112836A (fr)
NL (1)	NL8204996A (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA1210928A (fr) *	1982-09-20	1986-09-09	Arnold M. Singer	Methode et systeme de decontamination d'un fluide de forage
US4552672A (en) *	1984-06-21	1985-11-12	Halliburton Company	Method and composition for acidizing subterranean formations
WO1996003474A1 (fr) *	1994-07-27	1996-02-08	Baker Hughes Incorporated	Additifs de boues de forage pour une stabilisation amelioree des schistes, boues de forage ainsi formees et utilisation de ces dernieres

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3126950A (en) *		1964-03-31		Steel coupons in
US3107221A (en) *	1958-04-18	1963-10-15	Dow Chemical Co	Corrosion inhibitor composition
US4304677A (en) *	1978-09-05	1981-12-08	The Dow Chemical Company	Method of servicing wellbores
US4292183A (en) *	1978-12-13	1981-09-29	Great Lakes Chemical Corporation	High-density fluid compositions

1982
- 1982-12-01 CA CA000416810A patent/CA1201282A/fr not_active Expired
- 1982-12-01 GB GB08234302A patent/GB2112836A/en not_active Withdrawn
- 1982-12-23 DE DE19823247872 patent/DE3247872A1/de not_active Ceased
- 1982-12-27 NL NL8204996A patent/NL8204996A/nl not_active Application Discontinuation

Also Published As

Publication number	Publication date
DE3247872A1 (de)	1983-07-07
NL8204996A (nl)	1983-07-18
GB2112836A (en)	1983-07-27

Legal Events

Date	Code	Title	Description
2003-03-04	MKEX	Expiry

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US20110100630A1 (en)	2011-05-05	Method of Mitigating Corrosion Rate of Oilfield Tubular Goods
US4522658A (en)	1985-06-11	Method and composition for protecting metal surfaces from oxidative environments
US6068056A (en)	2000-05-30	Well treatment fluids comprising mixed aldehydes
US5441929A (en)	1995-08-15	Hydrochloric acid acidizing composition and method
CA1130552A (fr)	1982-08-31	Bromures de zinc et de calcium servant a la completion des puits
US6180057B1 (en)	2001-01-30	Corrosion inhibiting compositions and methods
US7655158B2 (en)	2010-02-02	Corrosion inhibitor
US5976416A (en)	1999-11-02	Corrosion inhibited organic acid compositions and methods
US4574050A (en)	1986-03-04	Method for preventing the precipitation of ferric compounds during the acid treatment of wells
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