NO820015L - Fremgangsmaate og sammensetninger for behandling av permeable formasjoner - Google Patents
Fremgangsmaate og sammensetninger for behandling av permeable formasjonerInfo
- Publication number
- NO820015L NO820015L NO820015A NO820015A NO820015L NO 820015 L NO820015 L NO 820015L NO 820015 A NO820015 A NO 820015A NO 820015 A NO820015 A NO 820015A NO 820015 L NO820015 L NO 820015L
- Authority
- NO
- Norway
- Prior art keywords
- polymer
- cationic
- viscosity
- carbon atoms
- polymers
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 28
- 238000000034 method Methods 0.000 title claims description 17
- 238000011282 treatment Methods 0.000 title description 3
- 229920000642 polymer Polymers 0.000 claims description 233
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 62
- 229920006317 cationic polymer Polymers 0.000 claims description 39
- 229910052757 nitrogen Inorganic materials 0.000 claims description 39
- 230000015572 biosynthetic process Effects 0.000 claims description 38
- 125000005842 heteroatom Chemical group 0.000 claims description 38
- 125000002091 cationic group Chemical group 0.000 claims description 37
- 125000004432 carbon atom Chemical group C* 0.000 claims description 34
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 32
- 229920000620 organic polymer Polymers 0.000 claims description 30
- 150000003254 radicals Chemical class 0.000 claims description 27
- 125000000217 alkyl group Chemical group 0.000 claims description 24
- 239000007788 liquid Substances 0.000 claims description 24
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 23
- 229910052698 phosphorus Inorganic materials 0.000 claims description 23
- 239000011574 phosphorus Substances 0.000 claims description 23
- 229910052717 sulfur Inorganic materials 0.000 claims description 22
- 239000001257 hydrogen Substances 0.000 claims description 21
- 229910052739 hydrogen Inorganic materials 0.000 claims description 21
- 239000011593 sulfur Substances 0.000 claims description 20
- 238000011084 recovery Methods 0.000 claims description 19
- 229920002851 polycationic polymer Polymers 0.000 claims description 18
- 150000001450 anions Chemical class 0.000 claims description 17
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 17
- 229930195733 hydrocarbon Natural products 0.000 claims description 17
- 229910052760 oxygen Inorganic materials 0.000 claims description 17
- 239000001301 oxygen Substances 0.000 claims description 17
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 13
- 239000004927 clay Substances 0.000 claims description 13
- 150000002430 hydrocarbons Chemical class 0.000 claims description 13
- 239000004215 Carbon black (E152) Substances 0.000 claims description 12
- 239000005864 Sulphur Substances 0.000 claims description 12
- 125000001931 aliphatic group Chemical group 0.000 claims description 12
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 9
- 229920003169 water-soluble polymer Polymers 0.000 claims description 9
- 125000004429 atom Chemical group 0.000 claims description 8
- 238000006073 displacement reaction Methods 0.000 claims description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 8
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 7
- 150000002431 hydrogen Chemical group 0.000 claims description 6
- 229910052751 metal Chemical group 0.000 claims description 6
- 239000002184 metal Chemical group 0.000 claims description 6
- YZCKVEUIGOORGS-IGMARMGPSA-N Protium Chemical compound [1H] YZCKVEUIGOORGS-IGMARMGPSA-N 0.000 claims description 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 5
- 229920002959 polymer blend Polymers 0.000 claims description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 4
- 150000001408 amides Chemical class 0.000 claims description 4
- 150000001412 amines Chemical class 0.000 claims description 4
- 125000004122 cyclic group Chemical group 0.000 claims description 4
- 230000000737 periodic effect Effects 0.000 claims description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 3
- 229910052794 bromium Inorganic materials 0.000 claims description 3
- 239000000460 chlorine Substances 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 3
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- 239000011737 fluorine Substances 0.000 claims description 3
- 239000011630 iodine Substances 0.000 claims description 3
- 229910052740 iodine Inorganic materials 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- 150000002500 ions Chemical class 0.000 claims 2
- 239000011236 particulate material Substances 0.000 claims 1
- 239000011435 rock Substances 0.000 claims 1
- 239000003381 stabilizer Substances 0.000 claims 1
- 229920003170 water-soluble synthetic polymer Polymers 0.000 claims 1
- 239000002023 wood Substances 0.000 claims 1
- 239000000243 solution Substances 0.000 description 65
- -1 CO 2 or N 2 ) Substances 0.000 description 53
- 238000005755 formation reaction Methods 0.000 description 31
- 229920002401 polyacrylamide Polymers 0.000 description 30
- 239000003921 oil Substances 0.000 description 28
- 125000003118 aryl group Chemical group 0.000 description 20
- 239000000945 filler Substances 0.000 description 19
- 239000012530 fluid Substances 0.000 description 18
- 238000001179 sorption measurement Methods 0.000 description 16
- 239000000178 monomer Substances 0.000 description 14
- 150000001768 cations Chemical class 0.000 description 13
- 229920001577 copolymer Polymers 0.000 description 13
- 239000007787 solid Substances 0.000 description 13
- 125000002947 alkylene group Chemical group 0.000 description 10
- 230000000694 effects Effects 0.000 description 9
- 125000000623 heterocyclic group Chemical group 0.000 description 9
- 230000015556 catabolic process Effects 0.000 description 8
- 239000007859 condensation product Substances 0.000 description 8
- 150000004820 halides Chemical class 0.000 description 8
- 238000002347 injection Methods 0.000 description 8
- 239000007924 injection Substances 0.000 description 8
- 125000001424 substituent group Chemical group 0.000 description 8
- 229910002651 NO3 Inorganic materials 0.000 description 7
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 7
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 7
- 230000007062 hydrolysis Effects 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 7
- 239000002244 precipitate Substances 0.000 description 7
- 229910021647 smectite Inorganic materials 0.000 description 7
- 238000006460 hydrolysis reaction Methods 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 125000004433 nitrogen atom Chemical group N* 0.000 description 6
- 230000009467 reduction Effects 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 125000003342 alkenyl group Chemical group 0.000 description 5
- 125000000129 anionic group Chemical group 0.000 description 5
- 238000005553 drilling Methods 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 5
- 239000013505 freshwater Substances 0.000 description 5
- 239000010410 layer Substances 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 229920001059 synthetic polymer Polymers 0.000 description 5
- 229920001897 terpolymer Polymers 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 229910019142 PO4 Inorganic materials 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 238000006731 degradation reaction Methods 0.000 description 4
- 229910052736 halogen Inorganic materials 0.000 description 4
- 150000002367 halogens Chemical class 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 4
- 235000021317 phosphate Nutrition 0.000 description 4
- 150000003457 sulfones Chemical class 0.000 description 4
- 229920001285 xanthan gum Polymers 0.000 description 4
- 239000000230 xanthan gum Substances 0.000 description 4
- 235000010493 xanthan gum Nutrition 0.000 description 4
- 229940082509 xanthan gum Drugs 0.000 description 4
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 3
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 3
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 150000007942 carboxylates Chemical group 0.000 description 3
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- 229920000371 poly(diallyldimethylammonium chloride) polymer Polymers 0.000 description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 239000012266 salt solution Substances 0.000 description 3
- 239000004576 sand Substances 0.000 description 3
- 238000007789 sealing Methods 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
- 229920000209 Hexadimethrine bromide Polymers 0.000 description 2
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 229920006322 acrylamide copolymer Polymers 0.000 description 2
- 125000004450 alkenylene group Chemical group 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- 125000000304 alkynyl group Chemical group 0.000 description 2
- 125000004419 alkynylene group Chemical group 0.000 description 2
- 150000001540 azides Chemical class 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 150000001805 chlorine compounds Chemical group 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- 125000004185 ester group Chemical group 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical compound OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 229940088644 n,n-dimethylacrylamide Drugs 0.000 description 2
- YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 description 2
- YPHQUSNPXDGUHL-UHFFFAOYSA-N n-methylprop-2-enamide Chemical compound CNC(=O)C=C YPHQUSNPXDGUHL-UHFFFAOYSA-N 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 229920002939 poly(N,N-dimethylacrylamides) Polymers 0.000 description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
- 239000004926 polymethyl methacrylate Substances 0.000 description 2
- 229920001282 polysaccharide Polymers 0.000 description 2
- 239000005017 polysaccharide Substances 0.000 description 2
- 150000004804 polysaccharides Chemical class 0.000 description 2
- 238000005086 pumping Methods 0.000 description 2
- 238000010850 salt effect Methods 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 125000004434 sulfur atom Chemical group 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 230000002195 synergetic effect Effects 0.000 description 2
- 230000008719 thickening Effects 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- ULTHEAFYOOPTTB-UHFFFAOYSA-N 1,4-dibromobutane Chemical compound BrCCCCBr ULTHEAFYOOPTTB-UHFFFAOYSA-N 0.000 description 1
- KJDRSWPQXHESDQ-UHFFFAOYSA-N 1,4-dichlorobutane Chemical compound ClCCCCCl KJDRSWPQXHESDQ-UHFFFAOYSA-N 0.000 description 1
- HZONRRHNQILCNO-UHFFFAOYSA-N 1-methyl-2h-pyridine Chemical compound CN1CC=CC=C1 HZONRRHNQILCNO-UHFFFAOYSA-N 0.000 description 1
- WSZKYTLBECKZHI-UHFFFAOYSA-N 2-[4-[2-(dimethylamino)ethyl]phenyl]-N,N-dimethylethanamine Chemical compound CN(C)CCC1=CC=C(C=C1)CCN(C)C WSZKYTLBECKZHI-UHFFFAOYSA-N 0.000 description 1
- AUGHIHYKUVKATF-UHFFFAOYSA-N 4-(3-chloropropyl)pyridine Chemical compound ClCCCC1=CC=NC=C1 AUGHIHYKUVKATF-UHFFFAOYSA-N 0.000 description 1
- PVMNPAUTCMBOMO-UHFFFAOYSA-N 4-chloropyridine Chemical compound ClC1=CC=NC=C1 PVMNPAUTCMBOMO-UHFFFAOYSA-N 0.000 description 1
- HEUUBYJSWGMIIU-UHFFFAOYSA-N 5,5-bis(chloromethyl)-2-phenylcyclohexa-1,3-diene Chemical group C1=CC(CCl)(CCl)CC=C1C1=CC=CC=C1 HEUUBYJSWGMIIU-UHFFFAOYSA-N 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- WSNMPAVSZJSIMT-UHFFFAOYSA-N COc1c(C)c2COC(=O)c2c(O)c1CC(O)C1(C)CCC(=O)O1 Chemical compound COc1c(C)c2COC(=O)c2c(O)c1CC(O)C1(C)CCC(=O)O1 WSNMPAVSZJSIMT-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 1
- 229920002907 Guar gum Polymers 0.000 description 1
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 1
- 229930194542 Keto Natural products 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 1
- 244000100205 Robinia Species 0.000 description 1
- 238000002441 X-ray diffraction Methods 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
- 238000010306 acid treatment Methods 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 150000001449 anionic compounds Chemical class 0.000 description 1
- 229920001586 anionic polysaccharide Polymers 0.000 description 1
- 150000004836 anionic polysaccharides Chemical class 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000000732 arylene group Chemical group 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- 239000002981 blocking agent Substances 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 125000002837 carbocyclic group Chemical group 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical class ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- IBAHLNWTOIHLKE-UHFFFAOYSA-N cyano cyanate Chemical compound N#COC#N IBAHLNWTOIHLKE-UHFFFAOYSA-N 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 229920006158 high molecular weight polymer Polymers 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 229910001412 inorganic anion Inorganic materials 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000010338 mechanical breakdown Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical class CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000003129 oil well Substances 0.000 description 1
- 150000002891 organic anions Chemical class 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920001483 poly(ethyl methacrylate) polymer Polymers 0.000 description 1
- 229920000120 polyethyl acrylate Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 229920005613 synthetic organic polymer Polymers 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 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
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/02—Well-drilling compositions
- C09K8/04—Aqueous well-drilling compositions
- C09K8/06—Clay-free compositions
- C09K8/12—Clay-free compositions containing synthetic organic macromolecular compounds or their precursors
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/50—Compositions for plastering borehole walls, i.e. compositions for temporary consolidation of borehole walls
- C09K8/504—Compositions based on water or polar solvents
- C09K8/506—Compositions based on water or polar solvents containing organic compounds
- C09K8/508—Compositions based on water or polar solvents containing organic compounds macromolecular compounds
-
- 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
- C09K8/58—Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids
- C09K8/588—Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids characterised by the use of specific polymers
-
- 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)
- Life Sciences & Earth Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Lubricants (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Separation Using Semi-Permeable Membranes (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/222,837 US4409110A (en) | 1981-01-06 | 1981-01-06 | Enhanced oil displacement processes and compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
NO820015L true NO820015L (no) | 1982-07-07 |
Family
ID=22833910
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO820015A NO820015L (no) | 1981-01-06 | 1982-01-05 | Fremgangsmaate og sammensetninger for behandling av permeable formasjoner |
Country Status (10)
Country | Link |
---|---|
US (1) | US4409110A (de) |
JP (1) | JPS58101994A (de) |
AU (1) | AU552941B2 (de) |
BR (1) | BR8200017A (de) |
CA (1) | CA1178040A (de) |
DE (1) | DE3200022A1 (de) |
GB (1) | GB2091320B (de) |
MY (1) | MY8600362A (de) |
NL (1) | NL8200009A (de) |
NO (1) | NO820015L (de) |
Families Citing this family (55)
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---|---|---|---|---|
US4447342A (en) * | 1982-04-19 | 1984-05-08 | Halliburton Co. | Method of clay stabilization in enhanced oil recovery |
US4495367A (en) * | 1982-07-06 | 1985-01-22 | Celanese Corporation | High charge density, cationic methacrylamide based monomers and their _polymers |
DE3462059D1 (en) * | 1983-06-22 | 1987-02-19 | Halliburton Co | Anionic polymer composition and its use for stimulating a subterranean formation |
US4527628A (en) * | 1983-08-15 | 1985-07-09 | Halliburton Company | Method of temporarily plugging portions of a subterranean formation using a diverting agent |
IT1203717B (it) * | 1983-12-19 | 1989-02-23 | Sabo Spa | Addensante composito |
CA1235141A (en) * | 1984-03-28 | 1988-04-12 | Laurence G. Dammann | High charge density, cationic methacrylamide based monomers and their polymers |
US4626363A (en) * | 1984-08-29 | 1986-12-02 | National Starch And Chemical Corporation | Cationic acrylamide emulsion polymer brine thickeners |
US4604217A (en) * | 1984-09-13 | 1986-08-05 | Hercules Incorporated | Gelled aqueous compositions |
US4579667A (en) * | 1984-11-07 | 1986-04-01 | Hercules Incorporated | Gelled aqueous compositions |
US4617132A (en) * | 1985-04-01 | 1986-10-14 | Halliburton Company | Method of altering the permeability of a hydrocarbon-containing subterranean formation |
US4662444A (en) * | 1985-04-17 | 1987-05-05 | Standard Oil Company | Process for reducing polymer plugging during polymer injection into oil reservoir |
US4638865A (en) * | 1985-05-30 | 1987-01-27 | The Standard Oil Company | Bioresistant water-soluble alkyl substituted acrylamide polymers and enhanced oil recovery method employing same |
FR2585712B1 (fr) * | 1985-07-31 | 1989-11-24 | Sandoz Sa | Melanges de polymeres d'addition vinyliques utilisables comme agents de floculation et de deshydratation |
US4852652A (en) * | 1988-05-24 | 1989-08-01 | Chevron Research Company | Chemical flooding with improved injectivity |
GB8911519D0 (en) * | 1989-05-19 | 1989-07-05 | Allied Colloids Ltd | Polymeric compositions |
AU736803B2 (en) * | 1997-08-06 | 2001-08-02 | Halliburton Energy Services, Inc. | Well treating fluids and methods |
WO2000027944A1 (en) * | 1998-11-06 | 2000-05-18 | Baker Hughes Incorporated | Drilling fluid systems with improved fluid loss properties |
BR9904294B1 (pt) | 1999-09-22 | 2012-12-11 | processo para a redução seletiva e controlada da permeabilidade relativa à água em formações petrolìferas. | |
US7439209B2 (en) * | 1999-11-05 | 2008-10-21 | Baker Hughes Incorporated | Drilling fluid systems with improved fluid loss properties |
US7183239B2 (en) | 2001-12-12 | 2007-02-27 | Clearwater International, Llc | Gel plugs and pigs for pipeline use |
US8273693B2 (en) | 2001-12-12 | 2012-09-25 | Clearwater International Llc | Polymeric gel system and methods for making and using same in hydrocarbon recovery |
US7205262B2 (en) * | 2001-12-12 | 2007-04-17 | Weatherford/Lamb, Inc. | Friction reducing composition and method |
US7405188B2 (en) | 2001-12-12 | 2008-07-29 | Wsp Chemicals & Technology, Llc | Polymeric gel system and compositions for treating keratin substrates containing same |
EP1728843B1 (de) | 2001-12-12 | 2009-04-08 | Clearwater International, L.L.C | Reibungsreduzierende Zusammensetzung und zugehöriges Verfahren |
US20030114315A1 (en) * | 2001-12-12 | 2003-06-19 | Clearwater, Inc. | Polymeric gel system and use in hydrocarbon recovery |
US7741251B2 (en) | 2002-09-06 | 2010-06-22 | Halliburton Energy Services, Inc. | Compositions and methods of stabilizing subterranean formations containing reactive shales |
US7157409B2 (en) * | 2002-09-25 | 2007-01-02 | M-I Llc | Surfactant-polymer compositions for enhancing the stability of viscoelastic-surfactant based fluid |
AU2003285254A1 (en) * | 2002-12-02 | 2004-06-23 | Genesis International Oilfield Services Inc. | Drilling fluid and methods of use thereof |
US7759292B2 (en) | 2003-05-16 | 2010-07-20 | Halliburton Energy Services, Inc. | Methods and compositions for reducing the production of water and stimulating hydrocarbon production from a subterranean formation |
US8278250B2 (en) * | 2003-05-16 | 2012-10-02 | Halliburton Energy Services, Inc. | Methods useful for diverting aqueous fluids in subterranean operations |
US8181703B2 (en) | 2003-05-16 | 2012-05-22 | Halliburton Energy Services, Inc. | Method useful for controlling fluid loss in subterranean formations |
US8091638B2 (en) | 2003-05-16 | 2012-01-10 | Halliburton Energy Services, Inc. | Methods useful for controlling fluid loss in subterranean formations |
US8631869B2 (en) | 2003-05-16 | 2014-01-21 | Leopoldo Sierra | Methods useful for controlling fluid loss in subterranean treatments |
US7528095B2 (en) * | 2005-02-04 | 2009-05-05 | Halliburton Energy Services, Inc. | Methods and compositions for improving the thermal stability of aqueous polymeric wellbore treatment fluids |
US7541316B2 (en) * | 2005-02-04 | 2009-06-02 | Halliburton Energy Services, Inc. | Wellbore treatment fluids having improved thermal stability |
BRPI0708920B1 (pt) * | 2006-03-27 | 2018-05-02 | Shell Internationale Research Maatschappij B.V. | Sistema e método de injeção de água |
EP2139933A4 (de) * | 2007-03-23 | 2012-01-11 | Univ Texas | Verfahren zur behandlung einer formation mit einem lösungsmittel |
EP2132240A4 (de) * | 2007-03-23 | 2010-03-10 | Univ Texas | Zusammensetzungen und verfahren zur behandlung eines durch wasser blockierten bohrlochs |
EP2134806A4 (de) * | 2007-03-23 | 2011-08-03 | Univ Texas | Verfahren zur behandlung einer kohlenwasserstoffformation |
RU2009136515A (ru) * | 2007-03-23 | 2011-04-27 | Борд Оф Риджентс, Зе Юниверсити Оф Техас Систем (Us) | Способ и система для обработки углеводородных формаций |
MX2009010142A (es) * | 2007-03-23 | 2010-03-22 | Univ Texas | Composiciones y metodos para tratar un pozo de agua bloqueado. |
EA200970886A1 (ru) * | 2007-03-23 | 2010-10-29 | Эм-Ай Эл.Эл.Си. | Буровые растворы на водной основе для применений при высокой температуре - высоком давлении и способы применения |
US8099997B2 (en) | 2007-06-22 | 2012-01-24 | Weatherford/Lamb, Inc. | Potassium formate gel designed for the prevention of water ingress and dewatering of pipelines or flowlines |
US8065905B2 (en) | 2007-06-22 | 2011-11-29 | Clearwater International, Llc | Composition and method for pipeline conditioning and freezing point suppression |
US8261825B2 (en) * | 2007-11-30 | 2012-09-11 | Board Of Regents, The University Of Texas System | Methods for improving the productivity of oil producing wells |
US7932214B2 (en) | 2008-11-14 | 2011-04-26 | Clearwater International, Llc | Foamed gel systems for fracturing subterranean formations, and methods for making and using same |
WO2010147901A1 (en) * | 2009-06-15 | 2010-12-23 | Conocophillips Company-Ip Services Group | Swellable polymer with cationic sites |
US8394872B2 (en) * | 2009-07-10 | 2013-03-12 | Nalco Company | Method of reducing the viscosity of hydrocarbon fluids |
US20120252707A1 (en) * | 2011-03-30 | 2012-10-04 | Leiming Li | Methods and compositions to delay viscosification of treatment fluids |
CN102676144B (zh) * | 2012-05-10 | 2013-12-04 | 中国石油天然气股份有限公司 | 驱渗型采油剂用组合物及驱渗型采油剂 |
CN103320112B (zh) * | 2013-06-26 | 2015-12-09 | 西南石油大学 | 一种抗剪切树枝聚合物驱油剂及其合成方法 |
CN104155410B (zh) * | 2014-07-04 | 2015-12-02 | 中国石油天然气股份有限公司 | 一种洗油效率测试装置 |
CN110257042B (zh) * | 2019-07-06 | 2021-06-04 | 西南石油大学 | 一种储层自动破胶的清洁压裂液及其制备方法 |
CN110257043B (zh) * | 2019-07-06 | 2021-06-04 | 西南石油大学 | 一种刺激响应型清洁压裂液及其制备方法 |
US11685852B2 (en) | 2020-09-03 | 2023-06-27 | Aramco Services Company | Reservoir drilling fluids consist of cationic heterocyclic polymers, synthesis, formulation, and applications |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2718497A (en) * | 1950-11-03 | 1955-09-20 | Union Oil Co | Drilling muds |
US2761843A (en) * | 1954-11-18 | 1956-09-04 | Gulf Research Development Co | Treatment of clays |
US3039529A (en) * | 1959-05-19 | 1962-06-19 | Dow Chemical Co | Secondary recovery of petroleum |
US3804173A (en) * | 1971-07-01 | 1974-04-16 | Dow Chemical Co | Method for reducing polymer adsorption in secondary oil recovery operations |
US3780806A (en) * | 1972-01-31 | 1973-12-25 | Nalco Chemical Co | Inverted mixed latex for water flooding |
US3923666A (en) * | 1973-02-26 | 1975-12-02 | Halliburton Co | Method and composition for acidizing and fracturing wells |
US4191657A (en) * | 1975-12-24 | 1980-03-04 | Phillips Petroleum Company | Compositions for acidizing subterranean formations |
US4152274A (en) * | 1978-02-09 | 1979-05-01 | Nalco Chemical Company | Method for reducing friction loss in a well fracturing process |
-
1981
- 1981-01-06 US US06/222,837 patent/US4409110A/en not_active Expired - Fee Related
-
1982
- 1982-01-02 DE DE3200022A patent/DE3200022A1/de not_active Withdrawn
- 1982-01-05 NO NO820015A patent/NO820015L/no unknown
- 1982-01-05 BR BR8200017A patent/BR8200017A/pt unknown
- 1982-01-05 NL NL8200009A patent/NL8200009A/nl not_active Application Discontinuation
- 1982-01-05 CA CA000393592A patent/CA1178040A/en not_active Expired
- 1982-01-06 JP JP57000459A patent/JPS58101994A/ja active Pending
- 1982-01-06 GB GB8200245A patent/GB2091320B/en not_active Expired
- 1982-01-06 AU AU79241/82A patent/AU552941B2/en not_active Ceased
-
1986
- 1986-12-30 MY MY362/86A patent/MY8600362A/xx unknown
Also Published As
Publication number | Publication date |
---|---|
AU552941B2 (en) | 1986-06-26 |
GB2091320B (en) | 1985-07-31 |
US4409110A (en) | 1983-10-11 |
GB2091320A (en) | 1982-07-28 |
CA1178040A (en) | 1984-11-20 |
AU7924182A (en) | 1982-07-15 |
NL8200009A (nl) | 1982-08-02 |
BR8200017A (pt) | 1982-10-26 |
JPS58101994A (ja) | 1983-06-17 |
MY8600362A (en) | 1986-12-31 |
DE3200022A1 (de) | 1982-08-26 |
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