CA2342074C - Methode de traitement de schiste argileux et d'argile dans les formations productrices d'hydrocarbures - Google Patents

Methode de traitement de schiste argileux et d'argile dans les formations productrices d'hydrocarbures Download PDF

Info

Publication number: CA2342074C
Authority: CA; Canada
Prior art keywords: control additive; formation control; cationic; drilling fluid; formation
Prior art date: 2000-03-27
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

Application number

CA 2342074

Other languages

English (en)

Other versions

CA2342074A1 (fr

Inventor

Kevin W. Smith

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.)

Lubrizol Oilfield Solutions Inc

Original Assignee

Clearwater International Inc

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.)

2000-03-27

Filing date

2001-03-27

Publication date

2005-12-06

2001-03-27 Application filed by Clearwater International Inc filed Critical Clearwater International Inc

2001-09-27 Publication of CA2342074A1 publication Critical patent/CA2342074A1/fr

2005-12-06 Application granted granted Critical

2005-12-06 Publication of CA2342074C publication Critical patent/CA2342074C/fr

2021-03-27 Anticipated expiration legal-status Critical

Status Expired - Lifetime legal-status Critical Current

Links

230000015572 biosynthetic process Effects 0.000 title claims abstract description 101
239000004927 clay Substances 0.000 title abstract description 44
229930195733 hydrocarbon Natural products 0.000 title abstract description 6
150000002430 hydrocarbons Chemical class 0.000 title abstract description 6
239000004215 Carbon black (E152) Substances 0.000 title abstract description 5
238000005755 formation reaction Methods 0.000 title description 72
239000012530 fluid Substances 0.000 claims abstract description 80
239000000654 additive Substances 0.000 claims abstract description 60
230000000996 additive effect Effects 0.000 claims abstract description 41
125000002091 cationic group Chemical group 0.000 claims abstract description 40
238000005553 drilling Methods 0.000 claims abstract description 32
WFIZEGIEIOHZCP-UHFFFAOYSA-M potassium formate Chemical compound [K+].[O-]C=O WFIZEGIEIOHZCP-UHFFFAOYSA-M 0.000 claims abstract description 24
238000011282 treatment Methods 0.000 claims abstract description 21
-1 halide anion Chemical class 0.000 claims description 56
229920000642 polymer Polymers 0.000 claims description 22
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 12
150000001412 amines Chemical class 0.000 claims description 12
230000008961 swelling Effects 0.000 claims description 12
238000000034 method Methods 0.000 claims description 11
150000001450 anions Chemical class 0.000 claims description 9
GQOKIYDTHHZSCJ-UHFFFAOYSA-M dimethyl-bis(prop-2-enyl)azanium;chloride Chemical compound [Cl-].C=CC[N+](C)(C)CC=C GQOKIYDTHHZSCJ-UHFFFAOYSA-M 0.000 claims description 9
150000001875 compounds Chemical class 0.000 claims description 8
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims description 8
230000035699 permeability Effects 0.000 claims description 8
239000007864 aqueous solution Substances 0.000 claims description 6
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 4
OKIZCWYLBDKLSU-UHFFFAOYSA-M N,N,N-Trimethylmethanaminium chloride Chemical group [Cl-].C[N+](C)(C)C OKIZCWYLBDKLSU-UHFFFAOYSA-M 0.000 claims description 4
235000019253 formic acid Nutrition 0.000 claims description 4
238000011065 in-situ storage Methods 0.000 claims description 4
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 3
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 3
230000002411 adverse Effects 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
229920006317 cationic polymer Polymers 0.000 claims description 2
238000006243 chemical reaction Methods 0.000 claims description 2
229920001577 copolymer Polymers 0.000 claims description 2
239000011591 potassium Substances 0.000 claims description 2
229910052700 potassium Inorganic materials 0.000 claims description 2
229920001519 homopolymer Polymers 0.000 claims 3
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims 1
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims 1
229910000027 potassium carbonate Inorganic materials 0.000 claims 1
150000003856 quaternary ammonium compounds Chemical class 0.000 claims 1
238000004519 manufacturing process Methods 0.000 abstract description 4
125000004432 carbon atom Chemical group C* 0.000 description 15
235000002639 sodium chloride Nutrition 0.000 description 14
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
150000003839 salts Chemical class 0.000 description 13
150000004820 halides Chemical class 0.000 description 12
229910052757 nitrogen Inorganic materials 0.000 description 12
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
238000012360 testing method Methods 0.000 description 11
239000000463 material Substances 0.000 description 10
239000003349 gelling agent Substances 0.000 description 9
150000001768 cations Chemical class 0.000 description 7
239000007788 liquid Substances 0.000 description 7
241001539176 Hime Species 0.000 description 6
239000002734 clay mineral Substances 0.000 description 6
GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 6
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 6
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 5
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group 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 5
239000000470 constituent Substances 0.000 description 5
239000007789 gas Substances 0.000 description 5
229910052901 montmorillonite Inorganic materials 0.000 description 5
230000006641 stabilisation Effects 0.000 description 5
238000011105 stabilization Methods 0.000 description 5
230000000638 stimulation Effects 0.000 description 5
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 4
125000000217 alkyl group Chemical group 0.000 description 4
229910052799 carbon Inorganic materials 0.000 description 4
230000036571 hydration Effects 0.000 description 4
238000006703 hydration reaction Methods 0.000 description 4
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical group O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 4
229910017464 nitrogen compound Inorganic materials 0.000 description 4
229920002851 polycationic polymer Polymers 0.000 description 4
239000000126 substance Substances 0.000 description 4
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 3
125000000129 anionic group Chemical group 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
239000012141 concentrate Substances 0.000 description 3
230000001627 detrimental effect Effects 0.000 description 3
150000004676 glycans Chemical class 0.000 description 3
BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 3
238000005342 ion exchange Methods 0.000 description 3
150000002500 ions Chemical class 0.000 description 3
125000004433 nitrogen atom Chemical group N* 0.000 description 3
229920001282 polysaccharide Polymers 0.000 description 3
239000005017 polysaccharide Substances 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
125000001453 quaternary ammonium group Chemical group 0.000 description 3
239000011734 sodium Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
KFDVPJUYSDEJTH-UHFFFAOYSA-N 4-ethenylpyridine Chemical compound C=CC1=CC=NC=C1 KFDVPJUYSDEJTH-UHFFFAOYSA-N 0.000 description 2
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
244000007835 Cyamopsis tetragonoloba Species 0.000 description 2
NTYJJOPFIAHURM-UHFFFAOYSA-N Histamine Chemical compound NCCC1=CN=CN1 NTYJJOPFIAHURM-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical class C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
125000002877 alkyl aryl group Chemical group 0.000 description 2
239000011575 calcium Substances 0.000 description 2
229910052791 calcium Inorganic materials 0.000 description 2
229910052619 chlorite group Inorganic materials 0.000 description 2
QBWCMBCROVPCKQ-UHFFFAOYSA-N chlorous acid Chemical compound OCl=O QBWCMBCROVPCKQ-UHFFFAOYSA-N 0.000 description 2
LNEWRSKRTHQHKZ-UHFFFAOYSA-N dipropylazanium 2-hydroxypropane-1,2,3-tricarboxylate Chemical compound C(CC(O)(C(=O)[O-])CC(=O)[O-])(=O)[O-].C(CC)[NH2+]CCC.C(CC)[NH2+]CCC.C(CC)[NH2+]CCC LNEWRSKRTHQHKZ-UHFFFAOYSA-N 0.000 description 2
239000013505 freshwater Substances 0.000 description 2
229910052900 illite Inorganic materials 0.000 description 2
150000002460 imidazoles Chemical class 0.000 description 2
229910052742 iron Inorganic materials 0.000 description 2
229910052622 kaolinite Inorganic materials 0.000 description 2
GKQPCPXONLDCMU-CCEZHUSRSA-N lacidipine Chemical compound CCOC(=O)C1=C(C)NC(C)=C(C(=O)OCC)C1C1=CC=CC=C1\C=C\C(=O)OC(C)(C)C GKQPCPXONLDCMU-CCEZHUSRSA-N 0.000 description 2
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
239000006193 liquid solution Substances 0.000 description 2
239000011777 magnesium Substances 0.000 description 2
229910052749 magnesium Inorganic materials 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
150000002830 nitrogen compounds Chemical class 0.000 description 2
VGIBGUSAECPPNB-UHFFFAOYSA-L nonaaluminum;magnesium;tripotassium;1,3-dioxido-2,4,5-trioxa-1,3-disilabicyclo[1.1.1]pentane;iron(2+);oxygen(2-);fluoride;hydroxide Chemical compound [OH-].[O-2].[O-2].[O-2].[O-2].[O-2].[F-].[Mg+2].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[K+].[K+].[K+].[Fe+2].O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2 VGIBGUSAECPPNB-UHFFFAOYSA-L 0.000 description 2
239000001103 potassium chloride Substances 0.000 description 2
235000011164 potassium chloride Nutrition 0.000 description 2
159000000001 potassium salts Chemical class 0.000 description 2
239000002244 precipitate Substances 0.000 description 2
YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
239000000243 solution Substances 0.000 description 2
239000003381 stabilizer Substances 0.000 description 2
239000011593 sulfur Substances 0.000 description 2
229910052717 sulfur Inorganic materials 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
OMDQUFIYNPYJFM-XKDAHURESA-N (2r,3r,4s,5r,6s)-2-(hydroxymethyl)-6-[[(2r,3s,4r,5s,6r)-4,5,6-trihydroxy-3-[(2s,3s,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]methoxy]oxane-3,4,5-triol Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@@H]1OC[C@@H]1[C@@H](O[C@H]2[C@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)O)[C@H](O)[C@H](O)[C@H](O)O1 OMDQUFIYNPYJFM-XKDAHURESA-N 0.000 description 1
LUEWUZLMQUOBSB-FSKGGBMCSA-N (2s,3s,4s,5s,6r)-2-[(2r,3s,4r,5r,6s)-6-[(2r,3s,4r,5s,6s)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(2r,4r,5s,6r)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol Chemical compound O[C@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@@H](O[C@@H]2[C@H](O[C@@H](OC3[C@H](O[C@@H](O)[C@@H](O)[C@H]3O)CO)[C@@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O LUEWUZLMQUOBSB-FSKGGBMCSA-N 0.000 description 1
PBSBTNDGFDVAPR-UHFFFAOYSA-N 1-N,1-N-diethylpentane-1,4-diamine dihydrochloride Chemical compound Cl.Cl.CCN(CC)CCCC(C)N PBSBTNDGFDVAPR-UHFFFAOYSA-N 0.000 description 1
CYNYIHKIEHGYOZ-UHFFFAOYSA-N 1-bromopropane Chemical compound CCCBr CYNYIHKIEHGYOZ-UHFFFAOYSA-N 0.000 description 1
KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical class C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
JBHCEHKYXDXAIW-UHFFFAOYSA-N 3-methyl-n,n-bis(3-methylbutyl)butan-1-amine;hydrochloride Chemical compound Cl.CC(C)CCN(CCC(C)C)CCC(C)C JBHCEHKYXDXAIW-UHFFFAOYSA-N 0.000 description 1
RCJGSLQDTTUTKL-UHFFFAOYSA-N 3-methyl-n-(3-methylbutyl)butan-1-amine;hydrochloride Chemical compound Cl.CC(C)CCNCCC(C)C RCJGSLQDTTUTKL-UHFFFAOYSA-N 0.000 description 1
XMVQMBLTFKAIOX-UHFFFAOYSA-N 6-azaniumylhexylazanium;dichloride Chemical compound [Cl-].[Cl-].[NH3+]CCCCCC[NH3+] XMVQMBLTFKAIOX-UHFFFAOYSA-N 0.000 description 1
UBZXDFQTNLTDMC-UHFFFAOYSA-N 6-azaniumylhexylazanium;diiodide Chemical compound [I-].[I-].[NH3+]CCCCCC[NH3+] UBZXDFQTNLTDMC-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
ZFLWZOGXFQNIMT-UHFFFAOYSA-N 8-azaniumyloctylazanium;dichloride Chemical compound [Cl-].[Cl-].[NH3+]CCCCCCCC[NH3+] ZFLWZOGXFQNIMT-UHFFFAOYSA-N 0.000 description 1
102100036475 Alanine aminotransferase 1 Human genes 0.000 description 1
101710096214 Alanine aminotransferase 1 Proteins 0.000 description 1
102100033814 Alanine aminotransferase 2 Human genes 0.000 description 1
101710096000 Alanine aminotransferase 2 Proteins 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
229920000926 Galactomannan Polymers 0.000 description 1
229920002581 Glucomannan Polymers 0.000 description 1
229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
229910002651 NO3 Inorganic materials 0.000 description 1
NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 1
229920002873 Polyethylenimine Polymers 0.000 description 1
239000004113 Sepiolite Substances 0.000 description 1
244000166071 Shorea robusta Species 0.000 description 1
235000015076 Shorea robusta Nutrition 0.000 description 1
NJSSICCENMLTKO-HRCBOCMUSA-N [(1r,2s,4r,5r)-3-hydroxy-4-(4-methylphenyl)sulfonyloxy-6,8-dioxabicyclo[3.2.1]octan-2-yl] 4-methylbenzenesulfonate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)O[C@H]1C(O)[C@@H](OS(=O)(=O)C=2C=CC(C)=CC=2)[C@@H]2OC[C@H]1O2 NJSSICCENMLTKO-HRCBOCMUSA-N 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
MQFIKAWTCOXAAY-UHFFFAOYSA-N acetic acid;n-butylbutan-1-amine Chemical compound CC([O-])=O.CCCC[NH2+]CCCC MQFIKAWTCOXAAY-UHFFFAOYSA-N 0.000 description 1
LKDMDHMCNGRIAS-UHFFFAOYSA-N acetic acid;n-propylpropan-1-amine Chemical compound CC([O-])=O.CCC[NH2+]CCC LKDMDHMCNGRIAS-UHFFFAOYSA-N 0.000 description 1
SVBXPEXMMWJPIE-UHFFFAOYSA-N acetic acid;propan-1-amine Chemical compound CCC[NH3+].CC([O-])=O SVBXPEXMMWJPIE-UHFFFAOYSA-N 0.000 description 1
230000009471 action Effects 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
HPTYUNKZVDYXLP-UHFFFAOYSA-N aluminum;trihydroxy(trihydroxysilyloxy)silane;hydrate Chemical compound O.[Al].[Al].O[Si](O)(O)O[Si](O)(O)O HPTYUNKZVDYXLP-UHFFFAOYSA-N 0.000 description 1
235000019270 ammonium chloride Nutrition 0.000 description 1
150000003868 ammonium compounds Chemical class 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
229960000892 attapulgite Drugs 0.000 description 1
239000003899 bactericide agent Substances 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
230000008901 benefit Effects 0.000 description 1
HNGMUDYRDIQWNL-UHFFFAOYSA-N bis(2-methylpropyl)azanium formate Chemical compound C(=O)[O-].C(C(C)C)[NH2+]CC(C)C HNGMUDYRDIQWNL-UHFFFAOYSA-N 0.000 description 1
HDSBLUHKYYCLEZ-UHFFFAOYSA-N bis(2-methylpropyl)azanium;chloride Chemical compound Cl.CC(C)CNCC(C)C HDSBLUHKYYCLEZ-UHFFFAOYSA-N 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
RDHPKYGYEGBMSE-UHFFFAOYSA-N bromoethane Chemical compound CCBr RDHPKYGYEGBMSE-UHFFFAOYSA-N 0.000 description 1
239000001110 calcium chloride Substances 0.000 description 1
229910001628 calcium chloride Inorganic materials 0.000 description 1
150000001721 carbon Chemical group 0.000 description 1
238000005341 cation exchange Methods 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
230000008859 change Effects 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
XTEGARKTQYYJKE-UHFFFAOYSA-N chloric acid Chemical group OCl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-N 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
229910001919 chlorite Inorganic materials 0.000 description 1
239000003431 cross linking reagent Substances 0.000 description 1
239000013078 crystal Substances 0.000 description 1
DFHIFRBDQIFRFB-UHFFFAOYSA-N decane-1,10-diamine;dihydrochloride Chemical compound [Cl-].[Cl-].[NH3+]CCCCCCCCCC[NH3+] DFHIFRBDQIFRFB-UHFFFAOYSA-N 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
JQVDAXLFBXTEQA-UHFFFAOYSA-O dibutylazanium Chemical compound CCCC[NH2+]CCCC JQVDAXLFBXTEQA-UHFFFAOYSA-O 0.000 description 1
VBBBYENORSEJRN-UHFFFAOYSA-N dibutylazanium 2-hydroxypropanoate Chemical compound C(C(O)C)(=O)[O-].C(CCC)[NH2+]CCCC VBBBYENORSEJRN-UHFFFAOYSA-N 0.000 description 1
229910001649 dickite Inorganic materials 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
YIOJGTBNHQAVBO-UHFFFAOYSA-N dimethyl-bis(prop-2-enyl)azanium Chemical class C=CC[N+](C)(C)CC=C YIOJGTBNHQAVBO-UHFFFAOYSA-N 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
239000004088 foaming agent Substances 0.000 description 1
229910052631 glauconite Inorganic materials 0.000 description 1
229940046240 glucomannan Drugs 0.000 description 1
239000008187 granular material Substances 0.000 description 1
239000003673 groundwater Substances 0.000 description 1
229910052621 halloysite Inorganic materials 0.000 description 1
230000009931 harmful effect Effects 0.000 description 1
229910000271 hectorite Inorganic materials 0.000 description 1
KWLMIXQRALPRBC-UHFFFAOYSA-L hectorite Chemical compound [Li+].[OH-].[OH-].[Na+].[Mg+2].O1[Si]2([O-])O[Si]1([O-])O[Si]([O-])(O1)O[Si]1([O-])O2 KWLMIXQRALPRBC-UHFFFAOYSA-L 0.000 description 1
229920006158 high molecular weight polymer Polymers 0.000 description 1
229960001340 histamine Drugs 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000011630 iodine Substances 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
FMKOJHQHASLBPH-UHFFFAOYSA-N isopropyl iodide Chemical compound CC(C)I FMKOJHQHASLBPH-UHFFFAOYSA-N 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
239000002609 medium Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
239000011707 mineral Substances 0.000 description 1
239000000203 mixture Substances 0.000 description 1
239000000178 monomer Substances 0.000 description 1
PWLGUYGCKDLZNE-UHFFFAOYSA-N n',n'-diethylethane-1,2-diamine;dihydrochloride Chemical compound Cl.Cl.CCN(CC)CCN PWLGUYGCKDLZNE-UHFFFAOYSA-N 0.000 description 1
FHPLZNQQMWUDGI-UHFFFAOYSA-N n',n'-dimethylpropane-1,3-diamine;dihydrochloride Chemical compound Cl.Cl.CN(C)CCCN FHPLZNQQMWUDGI-UHFFFAOYSA-N 0.000 description 1
OKHMDSCYUWAQPT-UHFFFAOYSA-N n'-[2-(2-aminoethylamino)ethyl]ethane-1,2-diamine;tetrahydrochloride Chemical compound Cl.Cl.Cl.Cl.NCCNCCNCCN OKHMDSCYUWAQPT-UHFFFAOYSA-N 0.000 description 1
VGICAQBLDJAGSJ-UHFFFAOYSA-N n'-[2-[2-(2-aminoethylamino)ethylamino]ethyl]ethane-1,2-diamine;pentahydrochloride Chemical compound Cl.Cl.Cl.Cl.Cl.NCCNCCNCCNCCN VGICAQBLDJAGSJ-UHFFFAOYSA-N 0.000 description 1
XJIDPCDRTUZMEK-UHFFFAOYSA-N n'-propan-2-ylpropane-1,3-diamine;dihydrochloride Chemical compound Cl.Cl.CC(C)NCCCN XJIDPCDRTUZMEK-UHFFFAOYSA-N 0.000 description 1
ALGXBNKQANCVPJ-UHFFFAOYSA-N n,n-diheptylheptan-1-amine;hydrochloride Chemical compound Cl.CCCCCCCN(CCCCCCC)CCCCCCC ALGXBNKQANCVPJ-UHFFFAOYSA-N 0.000 description 1
HUKPSOLHZPASDU-UHFFFAOYSA-N n,n-dipropylpropan-1-amine;hydroiodide Chemical compound [I-].CCC[NH+](CCC)CCC HUKPSOLHZPASDU-UHFFFAOYSA-N 0.000 description 1
ODYNBECIRXXOGG-UHFFFAOYSA-N n-butylbutan-1-amine;hydron;chloride Chemical compound [Cl-].CCCC[NH2+]CCCC ODYNBECIRXXOGG-UHFFFAOYSA-N 0.000 description 1
FGISZQXBPYTXLX-UHFFFAOYSA-N n-heptylheptan-1-amine;hydrochloride Chemical compound Cl.CCCCCCCNCCCCCCC FGISZQXBPYTXLX-UHFFFAOYSA-N 0.000 description 1
JPZAYXNLNMYCAK-UHFFFAOYSA-N n-propylbutan-1-amine;hydrochloride Chemical compound Cl.CCCCNCCC JPZAYXNLNMYCAK-UHFFFAOYSA-N 0.000 description 1
GAZIBGHLWYHBDT-UHFFFAOYSA-N n-propylpropan-1-amine;hydrochloride Chemical compound Cl.CCCNCCC GAZIBGHLWYHBDT-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
229910017604 nitric acid Inorganic materials 0.000 description 1
229910000273 nontronite Inorganic materials 0.000 description 1
239000003129 oil well Substances 0.000 description 1
230000003204 osmotic effect Effects 0.000 description 1
229910052625 palygorskite Inorganic materials 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
239000002245 particle Substances 0.000 description 1
XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
150000004885 piperazines Chemical class 0.000 description 1
150000003053 piperidines Chemical class 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229920000371 poly(diallyldimethylammonium chloride) polymer Polymers 0.000 description 1
229920000768 polyamine Polymers 0.000 description 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
230000008569 process Effects 0.000 description 1
239000000047 product Substances 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
150000003222 pyridines Chemical class 0.000 description 1
JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical class C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 description 1
238000011084 recovery Methods 0.000 description 1
230000009467 reduction Effects 0.000 description 1
229960004889 salicylic acid Drugs 0.000 description 1
239000004576 sand Substances 0.000 description 1
229910000275 saponite Inorganic materials 0.000 description 1
229910000276 sauconite Inorganic materials 0.000 description 1
229910052624 sepiolite Inorganic materials 0.000 description 1
235000019355 sepiolite Nutrition 0.000 description 1
229910021647 smectite Inorganic materials 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
241000894007 species Species 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
238000003860 storage Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium group Chemical group [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
NHGXDBSUJJNIRV-UHFFFAOYSA-M tetrabutylammonium chloride Chemical compound [Cl-].CCCC[N+](CCCC)(CCCC)CCCC NHGXDBSUJJNIRV-UHFFFAOYSA-M 0.000 description 1
DPKBAXPHAYBPRL-UHFFFAOYSA-M tetrabutylazanium;iodide Chemical compound [I-].CCCC[N+](CCCC)(CCCC)CCCC DPKBAXPHAYBPRL-UHFFFAOYSA-M 0.000 description 1
HWCKGOZZJDHMNC-UHFFFAOYSA-M tetraethylammonium bromide Chemical compound [Br-].CC[N+](CC)(CC)CC HWCKGOZZJDHMNC-UHFFFAOYSA-M 0.000 description 1
YMBCJWGVCUEGHA-UHFFFAOYSA-M tetraethylammonium chloride Chemical compound [Cl-].CC[N+](CC)(CC)CC YMBCJWGVCUEGHA-UHFFFAOYSA-M 0.000 description 1
FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
AIYGROOHMGFEIL-UHFFFAOYSA-M tetrakis(2-methylpropyl)azanium;chloride Chemical compound [Cl-].CC(C)C[N+](CC(C)C)(CC(C)C)CC(C)C AIYGROOHMGFEIL-UHFFFAOYSA-M 0.000 description 1
BMKCBSPIAGPRBW-UHFFFAOYSA-M tetrakis(3-methylbutyl)azanium;iodide Chemical compound [I-].CC(C)CC[N+](CCC(C)C)(CCC(C)C)CCC(C)C BMKCBSPIAGPRBW-UHFFFAOYSA-M 0.000 description 1
FBEVECUEMUUFKM-UHFFFAOYSA-M tetrapropylazanium;chloride Chemical compound [Cl-].CCC[N+](CCC)(CCC)CCC FBEVECUEMUUFKM-UHFFFAOYSA-M 0.000 description 1
125000005208 trialkylammonium group Chemical group 0.000 description 1
BQKQNVDQJLRFLX-UHFFFAOYSA-M tributyl(3-methylbutyl)azanium;iodide Chemical compound [I-].CCCC[N+](CCCC)(CCCC)CCC(C)C BQKQNVDQJLRFLX-UHFFFAOYSA-M 0.000 description 1
ZAMCTDDIJFNXOH-UHFFFAOYSA-N tributylazanium;acetate Chemical compound CC(O)=O.CCCCN(CCCC)CCCC ZAMCTDDIJFNXOH-UHFFFAOYSA-N 0.000 description 1
KLBOFRLEHJAXIU-UHFFFAOYSA-N tributylazanium;chloride Chemical compound Cl.CCCCN(CCCC)CCCC KLBOFRLEHJAXIU-UHFFFAOYSA-N 0.000 description 1
ZHURJYCOQGPWBW-UHFFFAOYSA-O tributylazanium;nitrate Chemical compound [O-][N+]([O-])=O.CCCC[NH+](CCCC)CCCC ZHURJYCOQGPWBW-UHFFFAOYSA-O 0.000 description 1
XOKPOPWYLRKXEA-UHFFFAOYSA-N trihexylazanium;chloride Chemical compound Cl.CCCCCCN(CCCCCC)CCCCCC XOKPOPWYLRKXEA-UHFFFAOYSA-N 0.000 description 1
BMXILUZRCXPKOI-UHFFFAOYSA-N tripropylazanium;chloride Chemical compound Cl.CCCN(CCC)CCC BMXILUZRCXPKOI-UHFFFAOYSA-N 0.000 description 1
229910052902 vermiculite Inorganic materials 0.000 description 1
239000010455 vermiculite Substances 0.000 description 1
235000019354 vermiculite Nutrition 0.000 description 1
239000003643 water by type Substances 0.000 description 1
229920001285 xanthan gum Polymers 0.000 description 1
239000000230 xanthan gum Substances 0.000 description 1
235000010493 xanthan gum Nutrition 0.000 description 1
229940082509 xanthan gum Drugs 0.000 description 1

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Silicates, Zeolites, And Molecular Sieves (AREA)
Solid-Sorbent Or Filter-Aiding Compositions (AREA)

CA 2342074 2000-03-27 2001-03-27 Methode de traitement de schiste argileux et d'argile dans les formations productrices d'hydrocarbures Expired - Lifetime CA2342074C (fr)

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US19230400P	2000-03-27	2000-03-27
US60/192,304		2000-03-27

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CA2342074A1 CA2342074A1 (fr)	2001-09-27
CA2342074C true CA2342074C (fr)	2005-12-06

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Date	Code	Title	Description
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2021-05-31	MKEX	Expiry	Effective date: 20210329

Publication	Publication Date	Title
US4842073A (en)	1989-06-27	Fluid additive and method for treatment of subterranean formations
CA1317755C (fr)	1993-05-18	Procede de stabilisation de formations argileuses
EP0501776A1 (fr)	1992-09-02	Stabilisation de formations souterraines
US5197544A (en)	1993-03-30	Method for clay stabilization with quaternary amines
US5089151A (en)	1992-02-18	Fluid additive and method for treatment of subterranean formations
US5607902A (en)	1997-03-04	Method of treating shale and clay in hydrocarbon formation drilling
US5099923A (en)	1992-03-31	Clay stabilizing method for oil and gas well treatment
US5152906A (en)	1992-10-06	Clay stabilizing composition for oil and gas well treatment
EP2917301B1 (fr)	2019-01-09	Polyétheramines alkylées en tant qu'agents stabilisant l'argile
EP1243749B1 (fr)	2005-06-29	Procédé de traitement de schiste et d'argile dans le forage de formations d'hydrocarbures
US4366073A (en)	1982-12-28	Oil well treating method and composition
US4366074A (en)	1982-12-28	Oil well treating method and composition
US4366071A (en)	1982-12-28	Oil well treating method and composition
US4366072A (en)	1982-12-28	Oil well treating method and composition
US4374739A (en)	1983-02-22	Oil well treating method and composition
EP1212385B1 (fr)	2015-12-30	Sels d'ammonium quaternaire en tant qu'agents epaississants pour des systemes aqueux
US4462718A (en)	1984-07-31	Oil well treating method and composition
US20040235677A1 (en)	2004-11-25	Methods and compositions for stabilizing swelling clays or migrating fines in formations
US5211239A (en)	1993-05-18	Method of maintaining subterranean formation permeability and inhibiting clay swelling
US20050215439A1 (en)	2005-09-29	Clay stabilization in sub-surface formations
CA2342074C (fr)	2005-12-06	Methode de traitement de schiste argileux et d'argile dans les formations productrices d'hydrocarbures