NO840783L - Fremgangsmaate til mobilitetskontroll av spalte-, sliss- eller porestroemninger - Google Patents

Fremgangsmaate til mobilitetskontroll av spalte-, sliss- eller porestroemninger

Info

Publication number: NO840783L
Authority: NO; Norway
Prior art keywords: alkyl; denotes; effect; alkenyl; preferably methyl
Prior art date: 1983-03-02

Application number

NO840783A

Other languages

English (en)

Norwegian (no)

Inventor

Raimund Haas

Dieter Ohlendorf

Werner Interthal

Original Assignee

Hoechst Ag

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.)

1983-03-02

Filing date

1984-03-01

Publication date

1984-09-03

1984-03-01 Application filed by Hoechst Ag filed Critical Hoechst Ag

1984-09-03 Publication of NO840783L publication Critical patent/NO840783L/no

Links

238000000034 method Methods 0.000 title claims abstract description 13
239000011148 porous material Substances 0.000 claims abstract description 27
239000007864 aqueous solution Substances 0.000 claims abstract description 16
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 15
150000001450 anions Chemical class 0.000 claims abstract description 14
238000005259 measurement Methods 0.000 claims abstract description 12
239000010779 crude oil Substances 0.000 claims abstract description 6
239000001257 hydrogen Substances 0.000 claims abstract description 6
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 6
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 5
239000000460 chlorine Substances 0.000 claims abstract description 5
239000012736 aqueous medium Substances 0.000 claims abstract description 4
229910052794 bromium Inorganic materials 0.000 claims abstract description 4
239000003093 cationic surfactant Substances 0.000 claims abstract description 4
229910052801 chlorine Inorganic materials 0.000 claims abstract description 4
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 3
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract description 3
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 3
230000005684 electric field Effects 0.000 claims abstract description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 21
150000001875 compounds Chemical class 0.000 claims description 11
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
239000003513 alkali Substances 0.000 claims description 4
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
125000003342 alkenyl group Chemical group 0.000 claims description 2
229910052723 transition metal Inorganic materials 0.000 claims description 2
150000003624 transition metals Chemical class 0.000 claims description 2
AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 claims 1
230000007423 decrease Effects 0.000 abstract description 6
125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract description 4
150000001767 cationic compounds Chemical class 0.000 abstract description 3
238000004519 manufacturing process Methods 0.000 abstract description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
125000006527 (C1-C5) alkyl group Chemical group 0.000 abstract 1
125000006729 (C2-C5) alkenyl group Chemical group 0.000 abstract 1
239000003643 water by type Substances 0.000 abstract 1
230000000694 effects Effects 0.000 description 59
239000004094 surface-active agent Substances 0.000 description 44
239000000243 solution Substances 0.000 description 39
-1 benzoic acid anions Chemical class 0.000 description 21
150000003839 salts Chemical class 0.000 description 21
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 18
239000003792 electrolyte Substances 0.000 description 13
230000001965 increasing effect Effects 0.000 description 13
229920000642 polymer Polymers 0.000 description 9
239000002609 medium Substances 0.000 description 8
239000002245 particle Substances 0.000 description 7
238000003860 storage Methods 0.000 description 7
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 6
238000007792 addition Methods 0.000 description 6
125000005211 alkyl trimethyl ammonium group Chemical group 0.000 description 6
230000006872 improvement Effects 0.000 description 6
229960001860 salicylate Drugs 0.000 description 6
150000001768 cations Chemical class 0.000 description 5
239000000203 mixture Substances 0.000 description 5
YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 5
229910052709 silver Inorganic materials 0.000 description 5
239000004332 silver Substances 0.000 description 5
239000002904 solvent Substances 0.000 description 5
238000003756 stirring Methods 0.000 description 5
IJFXRHURBJZNAO-UHFFFAOYSA-M 3-hydroxybenzoate Chemical compound OC1=CC=CC(C([O-])=O)=C1 IJFXRHURBJZNAO-UHFFFAOYSA-M 0.000 description 4
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
239000002253 acid Substances 0.000 description 4
125000000217 alkyl group Chemical group 0.000 description 4
230000015572 biosynthetic process Effects 0.000 description 4
150000001732 carboxylic acid derivatives Chemical class 0.000 description 4
230000008859 change Effects 0.000 description 4
238000005755 formation reaction Methods 0.000 description 4
239000007788 liquid Substances 0.000 description 4
150000003873 salicylate salts Chemical class 0.000 description 4
239000000523 sample Substances 0.000 description 4
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical class C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
238000011835 investigation Methods 0.000 description 3
239000000693 micelle Substances 0.000 description 3
239000003208 petroleum Substances 0.000 description 3
239000002244 precipitate Substances 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
OENLEHTYJXMVBG-UHFFFAOYSA-N pyridine;hydrate Chemical compound [OH-].C1=CC=[NH+]C=C1 OENLEHTYJXMVBG-UHFFFAOYSA-N 0.000 description 3
YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical class OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 3
UKHWJBVVWVYFEY-UHFFFAOYSA-M silver;hydroxide Chemical compound [OH-].[Ag+] UKHWJBVVWVYFEY-UHFFFAOYSA-M 0.000 description 3
239000007787 solid Substances 0.000 description 3
238000005303 weighing Methods 0.000 description 3
XUHRVZXFBWDCFB-QRTDKPMLSA-N (3R)-4-[[(3S,6S,9S,12R,15S,18R,21R,24R,27R,28R)-12-(3-amino-3-oxopropyl)-6-[(2S)-butan-2-yl]-3-(2-carboxyethyl)-18-(hydroxymethyl)-28-methyl-9,15,21,24-tetrakis(2-methylpropyl)-2,5,8,11,14,17,20,23,26-nonaoxo-1-oxa-4,7,10,13,16,19,22,25-octazacyclooctacos-27-yl]amino]-3-[[(2R)-2-[[(3S)-3-hydroxydecanoyl]amino]-4-methylpentanoyl]amino]-4-oxobutanoic acid Chemical compound CCCCCCC[C@H](O)CC(=O)N[C@H](CC(C)C)C(=O)N[C@H](CC(O)=O)C(=O)N[C@@H]1[C@@H](C)OC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CCC(N)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CO)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC1=O)[C@@H](C)CC XUHRVZXFBWDCFB-QRTDKPMLSA-N 0.000 description 2
UKAPYNPLXZAGQD-UHFFFAOYSA-M 2-carboxyphenolate;1-hexadecylpyridin-1-ium Chemical compound OC1=CC=CC=C1C([O-])=O.CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 UKAPYNPLXZAGQD-UHFFFAOYSA-M 0.000 description 2
JFLDCETXOKFEJC-UHFFFAOYSA-M 2-carboxyphenolate;hexadecyl(trimethyl)azanium Chemical compound OC1=CC=CC=C1C([O-])=O.CCCCCCCCCCCCCCCC[N+](C)(C)C JFLDCETXOKFEJC-UHFFFAOYSA-M 0.000 description 2
DRBFLYQSFBQQQC-UHFFFAOYSA-M 2-carboxyphenolate;trimethyl(tetradecyl)azanium Chemical compound OC1=CC=CC=C1C([O-])=O.CCCCCCCCCCCCCC[N+](C)(C)C DRBFLYQSFBQQQC-UHFFFAOYSA-M 0.000 description 2
UPHOPMSGKZNELG-UHFFFAOYSA-N 2-hydroxynaphthalene-1-carboxylic acid Chemical class C1=CC=C2C(C(=O)O)=C(O)C=CC2=C1 UPHOPMSGKZNELG-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
102000008068 Tensins Human genes 0.000 description 2
108010088950 Tensins Proteins 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
230000009471 action Effects 0.000 description 2
239000000654 additive Substances 0.000 description 2
230000001419 dependent effect Effects 0.000 description 2
238000009826 distribution Methods 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
238000001704 evaporation Methods 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
239000000706 filtrate Substances 0.000 description 2
239000011521 glass Substances 0.000 description 2
150000004820 halides Chemical class 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
150000002500 ions Chemical class 0.000 description 2
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
WLGDAKIJYPIYLR-UHFFFAOYSA-N octane-1-sulfonic acid Chemical compound CCCCCCCCS(O)(=O)=O WLGDAKIJYPIYLR-UHFFFAOYSA-N 0.000 description 2
238000003825 pressing Methods 0.000 description 2
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
230000035945 sensitivity Effects 0.000 description 2
SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
239000011780 sodium chloride Substances 0.000 description 2
125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 2
238000012360 testing method Methods 0.000 description 2
230000008719 thickening Effects 0.000 description 2
GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
ZXSQEZNORDWBGZ-UHFFFAOYSA-N 1,3-dihydropyrrolo[2,3-b]pyridin-2-one Chemical compound C1=CN=C2NC(=O)CC2=C1 ZXSQEZNORDWBGZ-UHFFFAOYSA-N 0.000 description 1
SJJCQDRGABAVBB-UHFFFAOYSA-N 1-hydroxy-2-naphthoic acid Chemical compound C1=CC=CC2=C(O)C(C(=O)O)=CC=C21 SJJCQDRGABAVBB-UHFFFAOYSA-N 0.000 description 1
HNIWHQDKCXCAKS-UHFFFAOYSA-M 2-carboxyphenolate;trimethyl(octadecyl)azanium Chemical compound OC1=CC=CC=C1C([O-])=O.CCCCCCCCCCCCCCCCCC[N+](C)(C)C HNIWHQDKCXCAKS-UHFFFAOYSA-M 0.000 description 1
CIHKVMHPDDJIIP-UHFFFAOYSA-N 2-methylperoxybenzoic acid Chemical compound COOC1=CC=CC=C1C(O)=O CIHKVMHPDDJIIP-UHFFFAOYSA-N 0.000 description 1
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
YWLXLRUDGLRYDR-ZHPRIASZSA-N 5beta,20-epoxy-1,7beta,10beta,13alpha-tetrahydroxy-9-oxotax-11-ene-2alpha,4alpha-diyl 4-acetate 2-benzoate Chemical compound O([C@H]1[C@H]2[C@@](C([C@H](O)C3=C(C)[C@@H](O)C[C@]1(O)C3(C)C)=O)(C)[C@@H](O)C[C@H]1OC[C@]12OC(=O)C)C(=O)C1=CC=CC=C1 YWLXLRUDGLRYDR-ZHPRIASZSA-N 0.000 description 1
HCJMNOSIAGSZBM-UHFFFAOYSA-N 6-methylsalicylic acid Chemical compound CC1=CC=CC(O)=C1C(O)=O HCJMNOSIAGSZBM-UHFFFAOYSA-N 0.000 description 1
101100537690 Arabidopsis thaliana TPC1 gene Proteins 0.000 description 1
239000005711 Benzoic acid Substances 0.000 description 1
WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Natural products OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
101100247636 Caenorhabditis elegans rde-10 gene Proteins 0.000 description 1
239000006004 Quartz sand Substances 0.000 description 1
ABBQHOQBGMUPJH-UHFFFAOYSA-M Sodium salicylate Chemical compound [Na+].OC1=CC=CC=C1C([O-])=O ABBQHOQBGMUPJH-UHFFFAOYSA-M 0.000 description 1
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
IWUMQDQQJUEVTP-UHFFFAOYSA-N [NH4+].C1=CC=C2C=C(C([O-])=O)C(O)=CC2=C1 Chemical compound [NH4+].C1=CC=C2C=C(C([O-])=O)C(O)=CC2=C1 IWUMQDQQJUEVTP-UHFFFAOYSA-N 0.000 description 1
150000001447 alkali salts Chemical class 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
229940063284 ammonium salicylate Drugs 0.000 description 1
239000002585 base Substances 0.000 description 1
230000008901 benefit Effects 0.000 description 1
235000010233 benzoic acid Nutrition 0.000 description 1
QXJJQWWVWRCVQT-UHFFFAOYSA-K calcium;sodium;phosphate Chemical compound [Na+].[Ca+2].[O-]P([O-])([O-])=O QXJJQWWVWRCVQT-UHFFFAOYSA-K 0.000 description 1
150000007942 carboxylates Chemical class 0.000 description 1
101150008810 cch1 gene Proteins 0.000 description 1
NEUSVAOJNUQRTM-UHFFFAOYSA-N cetylpyridinium Chemical compound CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 NEUSVAOJNUQRTM-UHFFFAOYSA-N 0.000 description 1
229960001927 cetylpyridinium chloride Drugs 0.000 description 1
RLGQACBPNDBWTB-UHFFFAOYSA-N cetyltrimethylammonium ion Chemical compound CCCCCCCCCCCCCCCC[N+](C)(C)C RLGQACBPNDBWTB-UHFFFAOYSA-N 0.000 description 1
238000002144 chemical decomposition reaction Methods 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
230000008034 disappearance Effects 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
UCYFZDNMZYZSPN-UHFFFAOYSA-N docosyl(trimethyl)azanium Chemical compound CCCCCCCCCCCCCCCCCCCCCC[N+](C)(C)C UCYFZDNMZYZSPN-UHFFFAOYSA-N 0.000 description 1
238000000855 fermentation Methods 0.000 description 1
230000004151 fermentation Effects 0.000 description 1
238000001595 flow curve Methods 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000008398 formation water Substances 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
239000007789 gas Substances 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
XLDBWUJNMVZVAA-UHFFFAOYSA-M heptane-1-sulfonate;trimethyl(tetradecyl)azanium Chemical compound CCCCCCCS([O-])(=O)=O.CCCCCCCCCCCCCC[N+](C)(C)C XLDBWUJNMVZVAA-UHFFFAOYSA-M 0.000 description 1
AKRQHOWXVSDJEF-UHFFFAOYSA-N heptane-1-sulfonic acid Chemical class CCCCCCCS(O)(=O)=O AKRQHOWXVSDJEF-UHFFFAOYSA-N 0.000 description 1
NONMSYWZLALTCW-UHFFFAOYSA-N hexadecyl 4-ethoxy-2-hydroxy-3,5,6-trimethylbenzoate Chemical compound C(CCCCCCCCCCCCCCC)OC(C=1C(O)=C(C(=C(C=1C)C)OCC)C)=O NONMSYWZLALTCW-UHFFFAOYSA-N 0.000 description 1
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
239000000463 material Substances 0.000 description 1
229960001047 methyl salicylate Drugs 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
238000002156 mixing Methods 0.000 description 1
NHLUVTZJQOJKCC-UHFFFAOYSA-N n,n-dimethylhexadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCN(C)C NHLUVTZJQOJKCC-UHFFFAOYSA-N 0.000 description 1
238000006386 neutralization reaction Methods 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
BKIMMITUMNQMOS-UHFFFAOYSA-N nonane Chemical compound CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 1
238000012856 packing Methods 0.000 description 1
229920000233 poly(alkylene oxides) Polymers 0.000 description 1
229920002959 polymer blend Polymers 0.000 description 1
239000000047 product Substances 0.000 description 1
238000000746 purification Methods 0.000 description 1
FBBHPHRBJLLIFM-UHFFFAOYSA-N pyridin-1-ium-1-carboxylate Chemical compound [O-]C(=O)[N+]1=CC=CC=C1 FBBHPHRBJLLIFM-UHFFFAOYSA-N 0.000 description 1
AOJFQRQNPXYVLM-UHFFFAOYSA-N pyridin-1-ium;chloride Chemical compound [Cl-].C1=CC=[NH+]C=C1 AOJFQRQNPXYVLM-UHFFFAOYSA-N 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
230000009467 reduction Effects 0.000 description 1
229910052702 rhenium Inorganic materials 0.000 description 1
238000005185 salting out Methods 0.000 description 1
239000004576 sand Substances 0.000 description 1
150000003378 silver Chemical class 0.000 description 1
229910001958 silver carbonate Inorganic materials 0.000 description 1
LKZMBDSASOBTPN-UHFFFAOYSA-L silver carbonate Substances [Ag].[O-]C([O-])=O LKZMBDSASOBTPN-UHFFFAOYSA-L 0.000 description 1
229910001961 silver nitrate Inorganic materials 0.000 description 1
229960004025 sodium salicylate Drugs 0.000 description 1
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical class CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
PDSVZUAJOIQXRK-UHFFFAOYSA-N trimethyl(octadecyl)azanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)C PDSVZUAJOIQXRK-UHFFFAOYSA-N 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
- 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
- C09K3/00—Materials not provided for elsewhere
- 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
- Y10S507/936—Flooding the formation

Landscapes

Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
General Life Sciences & Earth Sciences (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Steroid Compounds (AREA)
Inorganic Fibers (AREA)
Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Pyridine Compounds (AREA)
Lubricants (AREA)

NO840783A 1983-03-02 1984-03-01 Fremgangsmaate til mobilitetskontroll av spalte-, sliss- eller porestroemninger NO840783L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19833307252 DE3307252A1 (de)	1983-03-02	1983-03-02	Verfahren zur mobilitaetskontrolle von spalt-, schlitz oder porestroemungen

Publications (1)

Publication Number	Publication Date
NO840783L true NO840783L (no)	1984-09-03

Family

ID=6192229

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO840783A NO840783L (no)	1983-03-02	1984-03-01	Fremgangsmaate til mobilitetskontroll av spalte-, sliss- eller porestroemninger

Country Status (6)

Country	Link
US (1)	US4584109A (fr)
EP (1)	EP0118089B1 (fr)
AT (1)	ATE22151T1 (fr)
CA (1)	CA1230474A (fr)
DE (2)	DE3307252A1 (fr)
NO (1)	NO840783L (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3431414A1 (de) *	1984-08-27	1986-02-27	Hoechst Ag, 6230 Frankfurt	Mobilitaetskontrolle von spalt-, schlitz- oder porenstroemungen
DE3827183A1 (de) *	1988-08-11	1990-02-15	Hoechst Ag	Mischungen von organischen ammonium-salzen und deren verwendung als stroemungsbeschleuniger
US20020063241A1 (en) *	2000-10-16	2002-05-30	Alink Bernardus Antonius Maria Oude	Corrosion inhibitor-drag reducer combinations

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3302713A (en) *	1965-07-06	1967-02-07	Exxon Production Research Co	Surfactant-waterflooding process
US3361213A (en) *	1965-09-13	1968-01-02	Mobil Oil Corp	Method of decreasing friction loss in turbulent liquids
FR2145416B1 (fr) *	1971-07-15	1976-05-28	Exxon Production Researc
GB1504789A (en) *	1975-12-02	1978-03-22	British Petroleum Co	Hydrocarbon/water mixtures
US4216097A (en) *	1977-07-15	1980-08-05	Mobil Oil Corporation	Waterflooding employing amphoteric surfactants
US4469608A (en) *	1978-05-30	1984-09-04	The Dow Chemical Company	Surfactant composition containing alkylated biphenylyl phenyl ether sulfonates
US4193452A (en) *	1978-08-07	1980-03-18	Mobil Oil Corporation	Waterflooding employing thickened aqueous liquids
CA1136839A (fr) *	1979-06-11	1982-12-07	Alexis A. Oswald	Recuperation accrue du petrole par l'emploi de cristaux liquides lyotrophes dans des milieux salins tres concentres
FR2496504A1 (fr) *	1980-12-23	1982-06-25	Somalor Ferrari Somafer Ets	Composition et procede permettant de recuperer et de valoriser des produits petroliers
US4502540A (en) *	1981-06-01	1985-03-05	Mobil Oil Corporation	Tertiary oil recovery
US4615825A (en) *	1981-10-30	1986-10-07	The Dow Chemical Company	Friction reduction using a viscoelastic surfactant
DE3212969A1 (de) *	1982-04-07	1983-10-13	Hoechst Ag, 6230 Frankfurt	Verfahren zur verminderung des reibungswiderstandes in stroemenden waessrigen medien
DE3224148A1 (de) *	1982-06-29	1983-12-29	Hoechst Ag, 6230 Frankfurt	Quartaere ammoniumsalze und deren verwendung als stroemungsbeschleuniger

1983
- 1983-03-02 DE DE19833307252 patent/DE3307252A1/de not_active Withdrawn
1984
- 1984-02-24 AT AT84101982T patent/ATE22151T1/de not_active IP Right Cessation
- 1984-02-24 EP EP84101982A patent/EP0118089B1/fr not_active Expired
- 1984-02-24 DE DE8484101982T patent/DE3460647D1/de not_active Expired
- 1984-02-29 US US06/584,648 patent/US4584109A/en not_active Expired - Fee Related
- 1984-03-01 CA CA000448606A patent/CA1230474A/fr not_active Expired
- 1984-03-01 NO NO840783A patent/NO840783L/no unknown

Also Published As

Publication number	Publication date
EP0118089A2 (fr)	1984-09-12
US4584109A (en)	1986-04-22
CA1230474A (fr)	1987-12-22
EP0118089A3 (en)	1985-01-16
DE3460647D1 (en)	1986-10-16
EP0118089B1 (fr)	1986-09-10
DE3307252A1 (de)	1984-09-06
ATE22151T1 (de)	1986-09-15

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NO157541B (no)	1987-12-28	Viskoes, tung saltopploesnig for anvendelse ved oljeboring, og fremgangsmaate for oekning av dens viskositet og hydratiseringshastighet.
US4394273A (en)	1983-07-19	Defoamers for aqueous liquids containing soluble zinc salts
NO845276L (no)	1985-07-01	Fluorerte quaternaere ammoniumforbindelser, fremgangsmaate til deres fremstilling og deres anvendelse som stroemningsakselatorer