NO322844B1 - Anvendelse av en sammensetning i en underjordisk formasjon. - Google Patents
Anvendelse av en sammensetning i en underjordisk formasjon. Download PDFInfo
- Publication number
- NO322844B1 NO322844B1 NO19982888A NO982888A NO322844B1 NO 322844 B1 NO322844 B1 NO 322844B1 NO 19982888 A NO19982888 A NO 19982888A NO 982888 A NO982888 A NO 982888A NO 322844 B1 NO322844 B1 NO 322844B1
- Authority
- NO
- Norway
- Prior art keywords
- amino
- vinylbenzyl
- ammonium
- inner salt
- chloride
- Prior art date
Links
- 230000015572 biosynthetic process Effects 0.000 title claims 4
- 239000000203 mixture Substances 0.000 title claims 4
- 150000003839 salts Chemical class 0.000 claims 34
- -1 alkyl radical Chemical class 0.000 claims 10
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 7
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims 6
- MSQACBWWAIBWIC-UHFFFAOYSA-N hydron;piperazine;chloride Chemical compound Cl.C1CNCCN1 MSQACBWWAIBWIC-UHFFFAOYSA-N 0.000 claims 5
- 239000000178 monomer Substances 0.000 claims 5
- 229920000642 polymer Polymers 0.000 claims 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 4
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical class OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims 4
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical class OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 claims 4
- 239000003431 cross linking reagent Substances 0.000 claims 4
- XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical class OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 claims 4
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical class OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims 4
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims 4
- KWTGXHDPIPNNHP-UHFFFAOYSA-N 3-[(4-ethenylphenyl)methyl-dimethylazaniumyl]propane-1-sulfonate Chemical compound [O-]S(=O)(=O)CCC[N+](C)(C)CC1=CC=C(C=C)C=C1 KWTGXHDPIPNNHP-UHFFFAOYSA-N 0.000 claims 3
- 235000019270 ammonium chloride Nutrition 0.000 claims 3
- 150000001875 compounds Chemical class 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 3
- 239000007788 liquid Substances 0.000 claims 3
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- NMWVJWPQBXMVQJ-UHFFFAOYSA-N (2-amino-2-oxoethyl)-[(4-ethenylphenyl)methyl]-diethylazanium;chloride Chemical compound [Cl-].NC(=O)C[N+](CC)(CC)CC1=CC=C(C=C)C=C1 NMWVJWPQBXMVQJ-UHFFFAOYSA-N 0.000 claims 2
- SUVVKJDRNPMMGY-UHFFFAOYSA-N (2-amino-2-oxoethyl)-[(4-ethenylphenyl)methyl]-dimethylazanium;chloride Chemical compound [Cl-].NC(=O)C[N+](C)(C)CC1=CC=C(C=C)C=C1 SUVVKJDRNPMMGY-UHFFFAOYSA-N 0.000 claims 2
- YVNNRQCAABDUMX-UHFFFAOYSA-N 1-(4-methylpiperazin-1-yl)prop-2-en-1-one Chemical compound CN1CCN(C(=O)C=C)CC1 YVNNRQCAABDUMX-UHFFFAOYSA-N 0.000 claims 2
- XLPJNCYCZORXHG-UHFFFAOYSA-N 1-morpholin-4-ylprop-2-en-1-one Chemical compound C=CC(=O)N1CCOCC1 XLPJNCYCZORXHG-UHFFFAOYSA-N 0.000 claims 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims 2
- 229920000536 2-Acrylamido-2-methylpropane sulfonic acid Polymers 0.000 claims 2
- XHZPRMZZQOIPDS-UHFFFAOYSA-N 2-Methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid Chemical compound OS(=O)(=O)CC(C)(C)NC(=O)C=C XHZPRMZZQOIPDS-UHFFFAOYSA-N 0.000 claims 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 2
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 claims 2
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical class NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 claims 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical group NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 2
- BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical class CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 claims 2
- ZLWIXHQNXRJBJF-UHFFFAOYSA-N CC[N+](CC)(CCCS([O-])(=O)=O)Cc1ccc(C=C)cc1 Chemical compound CC[N+](CC)(CCCS([O-])(=O)=O)Cc1ccc(C=C)cc1 ZLWIXHQNXRJBJF-UHFFFAOYSA-N 0.000 claims 2
- OOUVFKFHVDUXNI-UHFFFAOYSA-N CC[N+](CC)(CCCS([O-])(=O)=O)Cc1cccc(C=C)c1 Chemical compound CC[N+](CC)(CCCS([O-])(=O)=O)Cc1cccc(C=C)c1 OOUVFKFHVDUXNI-UHFFFAOYSA-N 0.000 claims 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims 2
- 229910002651 NO3 Inorganic materials 0.000 claims 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims 2
- 229910019142 PO4 Inorganic materials 0.000 claims 2
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims 2
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 claims 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims 2
- 229960001138 acetylsalicylic acid Drugs 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- 229910052782 aluminium Inorganic materials 0.000 claims 2
- 150000001450 anions Chemical group 0.000 claims 2
- 150000005840 aryl radicals Chemical class 0.000 claims 2
- 125000006267 biphenyl group Chemical group 0.000 claims 2
- 239000004927 clay Substances 0.000 claims 2
- KSMVZQYAVGTKIV-UHFFFAOYSA-N decanal Chemical compound CCCCCCCCCC=O KSMVZQYAVGTKIV-UHFFFAOYSA-N 0.000 claims 2
- 150000004820 halides Chemical class 0.000 claims 2
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 claims 2
- DOUHZFSGSXMPIE-UHFFFAOYSA-N hydroxidooxidosulfur(.) Chemical compound [O]SO DOUHZFSGSXMPIE-UHFFFAOYSA-N 0.000 claims 2
- 150000004693 imidazolium salts Chemical group 0.000 claims 2
- 150000002736 metal compounds Chemical class 0.000 claims 2
- 125000001624 naphthyl group Chemical group 0.000 claims 2
- ZQBAKBUEJOMQEX-UHFFFAOYSA-N phenyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 claims 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims 2
- 239000010452 phosphate Substances 0.000 claims 2
- ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical compound [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 claims 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims 2
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 claims 2
- 229910052726 zirconium Inorganic materials 0.000 claims 2
- DSCRLQVLVSEFRA-UHFFFAOYSA-N (2-amino-2-oxoethyl)-[(3-ethenylphenyl)methyl]-diethylazanium;chloride Chemical compound [Cl-].NC(=O)C[N+](CC)(CC)CC1=CC=CC(C=C)=C1 DSCRLQVLVSEFRA-UHFFFAOYSA-N 0.000 claims 1
- CEMOASSEWCYWTC-UHFFFAOYSA-N (2-amino-2-oxoethyl)-[(3-ethenylphenyl)methyl]-dimethylazanium;chloride Chemical compound [Cl-].NC(=O)C[N+](C)(C)CC1=CC=CC(C=C)=C1 CEMOASSEWCYWTC-UHFFFAOYSA-N 0.000 claims 1
- BZBZRKCIMJDMMF-UHFFFAOYSA-N (3-amino-3-oxopropyl)-[(3-ethenylphenyl)methyl]-diethylazanium;chloride Chemical compound [Cl-].NC(=O)CC[N+](CC)(CC)CC1=CC=CC(C=C)=C1 BZBZRKCIMJDMMF-UHFFFAOYSA-N 0.000 claims 1
- QYRDGGXVFWZVCK-UHFFFAOYSA-N (3-amino-3-oxopropyl)-[(3-ethenylphenyl)methyl]-dimethylazanium;chloride Chemical compound [Cl-].NC(=O)CC[N+](C)(C)CC1=CC=CC(C=C)=C1 QYRDGGXVFWZVCK-UHFFFAOYSA-N 0.000 claims 1
- XOCGIYVMJGVXQV-UHFFFAOYSA-N (3-amino-3-oxopropyl)-[(4-ethenylphenyl)methyl]-diethylazanium;chloride Chemical compound [Cl-].NC(=O)CC[N+](CC)(CC)CC1=CC=C(C=C)C=C1 XOCGIYVMJGVXQV-UHFFFAOYSA-N 0.000 claims 1
- QYDHGHRZWQHDGG-UHFFFAOYSA-N (3-amino-3-oxopropyl)-[(4-ethenylphenyl)methyl]-dimethylazanium;chloride Chemical compound [Cl-].NC(=O)CC[N+](C)(C)CC1=CC=C(C=C)C=C1 QYDHGHRZWQHDGG-UHFFFAOYSA-N 0.000 claims 1
- RYSXWUYLAWPLES-MTOQALJVSA-N (Z)-4-hydroxypent-3-en-2-one titanium Chemical compound [Ti].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O RYSXWUYLAWPLES-MTOQALJVSA-N 0.000 claims 1
- YOBOXHGSEJBUPB-MTOQALJVSA-N (z)-4-hydroxypent-3-en-2-one;zirconium Chemical compound [Zr].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O YOBOXHGSEJBUPB-MTOQALJVSA-N 0.000 claims 1
- ZWKOZHUCZYUJJU-UHFFFAOYSA-N 2-(3-ethenylimidazol-1-ium-1-yl)acetamide;chloride Chemical group [Cl-].NC(=O)C[N+]=1C=CN(C=C)C=1 ZWKOZHUCZYUJJU-UHFFFAOYSA-N 0.000 claims 1
- XHHXXUFDXRYMQI-UHFFFAOYSA-N 2-[bis(2-hydroxyethyl)amino]ethanol;titanium Chemical compound [Ti].OCCN(CCO)CCO XHHXXUFDXRYMQI-UHFFFAOYSA-N 0.000 claims 1
- 125000000979 2-amino-2-oxoethyl group Chemical group [H]C([*])([H])C(=O)N([H])[H] 0.000 claims 1
- OFYFURKXMHQOGG-UHFFFAOYSA-J 2-ethylhexanoate;zirconium(4+) Chemical compound [Zr+4].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O OFYFURKXMHQOGG-UHFFFAOYSA-J 0.000 claims 1
- MSYNCHLYGJCFFY-UHFFFAOYSA-B 2-hydroxypropane-1,2,3-tricarboxylate;titanium(4+) Chemical compound [Ti+4].[Ti+4].[Ti+4].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O MSYNCHLYGJCFFY-UHFFFAOYSA-B 0.000 claims 1
- ZFQCFWRSIBGRFL-UHFFFAOYSA-B 2-hydroxypropane-1,2,3-tricarboxylate;zirconium(4+) Chemical compound [Zr+4].[Zr+4].[Zr+4].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O ZFQCFWRSIBGRFL-UHFFFAOYSA-B 0.000 claims 1
- LYPJRFIBDHNQLY-UHFFFAOYSA-J 2-hydroxypropanoate;zirconium(4+) Chemical compound [Zr+4].CC(O)C([O-])=O.CC(O)C([O-])=O.CC(O)C([O-])=O.CC(O)C([O-])=O LYPJRFIBDHNQLY-UHFFFAOYSA-J 0.000 claims 1
- BDSSZTXPZHIYHM-UHFFFAOYSA-N 2-phenoxypropanoyl chloride Chemical compound ClC(=O)C(C)OC1=CC=CC=C1 BDSSZTXPZHIYHM-UHFFFAOYSA-N 0.000 claims 1
- KAUVYZUWJBDZKO-UHFFFAOYSA-N 3-(3-ethenylimidazol-1-ium-1-yl)propanamide;chloride Chemical compound [Cl-].NC(=O)CC[N+]=1C=CN(C=C)C=1 KAUVYZUWJBDZKO-UHFFFAOYSA-N 0.000 claims 1
- 125000000981 3-amino-3-oxopropyl group Chemical group [H]C([*])([H])C([H])([H])C(=O)N([H])[H] 0.000 claims 1
- XYXLVTOFQMOGPS-UHFFFAOYSA-N 4-(3-ethenylimidazol-1-ium-1-yl)butanamide;chloride Chemical compound [Cl-].NC(=O)CCC[N+]=1C=CN(C=C)C=1 XYXLVTOFQMOGPS-UHFFFAOYSA-N 0.000 claims 1
- XRSQZFJLEPBPOZ-UHFFFAOYSA-N 4-amino-2-methylbenzoic acid Chemical compound CC1=CC(N)=CC=C1C(O)=O XRSQZFJLEPBPOZ-UHFFFAOYSA-N 0.000 claims 1
- WUBBRNOQWQTFEX-UHFFFAOYSA-N 4-aminosalicylic acid Chemical compound NC1=CC=C(C(O)=O)C(O)=C1 WUBBRNOQWQTFEX-UHFFFAOYSA-N 0.000 claims 1
- 229940090248 4-hydroxybenzoic acid Drugs 0.000 claims 1
- OBKXEAXTFZPCHS-UHFFFAOYSA-N 4-phenylbutyric acid Chemical compound OC(=O)CCCC1=CC=CC=C1 OBKXEAXTFZPCHS-UHFFFAOYSA-N 0.000 claims 1
- DUFCMRCMPHIFTR-UHFFFAOYSA-N 5-(dimethylsulfamoyl)-2-methylfuran-3-carboxylic acid Chemical compound CN(C)S(=O)(=O)C1=CC(C(O)=O)=C(C)O1 DUFCMRCMPHIFTR-UHFFFAOYSA-N 0.000 claims 1
- ZUGAOYSWHHGDJY-UHFFFAOYSA-K 5-hydroxy-2,8,9-trioxa-1-aluminabicyclo[3.3.2]decane-3,7,10-trione Chemical compound [Al+3].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O ZUGAOYSWHHGDJY-UHFFFAOYSA-K 0.000 claims 1
- IJEFAHUDTLUXDY-UHFFFAOYSA-J 7,7-dimethyloctanoate;zirconium(4+) Chemical compound [Zr+4].CC(C)(C)CCCCCC([O-])=O.CC(C)(C)CCCCCC([O-])=O.CC(C)(C)CCCCCC([O-])=O.CC(C)(C)CCCCCC([O-])=O IJEFAHUDTLUXDY-UHFFFAOYSA-J 0.000 claims 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims 1
- WRAGBEWQGHCDDU-UHFFFAOYSA-M C([O-])([O-])=O.[NH4+].[Zr+] Chemical compound C([O-])([O-])=O.[NH4+].[Zr+] WRAGBEWQGHCDDU-UHFFFAOYSA-M 0.000 claims 1
- DIFRRDFLOIVPSU-UHFFFAOYSA-N CC(CC[N+](C)(C)CC1=CC=C(C=C)C=C1)S([O-])(=O)=O Chemical compound CC(CC[N+](C)(C)CC1=CC=C(C=C)C=C1)S([O-])(=O)=O DIFRRDFLOIVPSU-UHFFFAOYSA-N 0.000 claims 1
- FOOSSFUQMWFLRR-UHFFFAOYSA-N CC(CC[N+](C)(C)Cc1cccc(C=C)c1)S([O-])(=O)=O Chemical compound CC(CC[N+](C)(C)Cc1cccc(C=C)c1)S([O-])(=O)=O FOOSSFUQMWFLRR-UHFFFAOYSA-N 0.000 claims 1
- DOISMHLLFVYOQI-UHFFFAOYSA-N CC[N+](CC)(CCC(C)S([O-])(=O)=O)CC1=CC=C(C=C)C=C1 Chemical compound CC[N+](CC)(CCC(C)S([O-])(=O)=O)CC1=CC=C(C=C)C=C1 DOISMHLLFVYOQI-UHFFFAOYSA-N 0.000 claims 1
- MHVHYSNVCNTTCJ-UHFFFAOYSA-N CC[N+](CC)(CCC(C)S([O-])(=O)=O)CC1=CC=CC(C=C)=C1 Chemical compound CC[N+](CC)(CCC(C)S([O-])(=O)=O)CC1=CC=CC(C=C)=C1 MHVHYSNVCNTTCJ-UHFFFAOYSA-N 0.000 claims 1
- QPVPKNOCWHAWLL-UHFFFAOYSA-N CC[N+](CC)(CCCCS([O-])(=O)=O)CC1=CC=C(C=C)C=C1 Chemical compound CC[N+](CC)(CCCCS([O-])(=O)=O)CC1=CC=C(C=C)C=C1 QPVPKNOCWHAWLL-UHFFFAOYSA-N 0.000 claims 1
- CGZDDWRXDJXGSK-UHFFFAOYSA-N C[N+](C)(CCCCS([O-])(=O)=O)CC1=CC=C(C=C)C=C1 Chemical compound C[N+](C)(CCCCS([O-])(=O)=O)CC1=CC=C(C=C)C=C1 CGZDDWRXDJXGSK-UHFFFAOYSA-N 0.000 claims 1
- NSZVCXFCPSMFHL-UHFFFAOYSA-N C[N+](C)(CCCCS([O-])(=O)=O)CC1=CC=CC(C=C)=C1 Chemical compound C[N+](C)(CCCCS([O-])(=O)=O)CC1=CC=CC(C=C)=C1 NSZVCXFCPSMFHL-UHFFFAOYSA-N 0.000 claims 1
- WYUSPJFREFLMNX-UHFFFAOYSA-N C[N+](C)(CCCS([O-])(=O)=O)Cc1cccc(C=C)c1 Chemical compound C[N+](C)(CCCS([O-])(=O)=O)Cc1cccc(C=C)c1 WYUSPJFREFLMNX-UHFFFAOYSA-N 0.000 claims 1
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 claims 1
- XSISQURPIRTMAY-UHFFFAOYSA-N Hydroxyethyl glycine Chemical compound NCC(=O)OCCO XSISQURPIRTMAY-UHFFFAOYSA-N 0.000 claims 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims 1
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims 1
- FOUZISDNESEYLX-UHFFFAOYSA-N N-hydroxyethyl glycine Natural products OCCNCC(O)=O FOUZISDNESEYLX-UHFFFAOYSA-N 0.000 claims 1
- 229930040373 Paraformaldehyde Natural products 0.000 claims 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 claims 1
- IPBVNPXQWQGGJP-UHFFFAOYSA-N acetic acid phenyl ester Natural products CC(=O)OC1=CC=CC=C1 IPBVNPXQWQGGJP-UHFFFAOYSA-N 0.000 claims 1
- 150000007513 acids Chemical class 0.000 claims 1
- 150000001299 aldehydes Chemical class 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 229960004050 aminobenzoic acid Drugs 0.000 claims 1
- 229960004909 aminosalicylic acid Drugs 0.000 claims 1
- ZRIUUUJAJJNDSS-UHFFFAOYSA-N ammonium phosphates Chemical compound [NH4+].[NH4+].[NH4+].[O-]P([O-])([O-])=O ZRIUUUJAJJNDSS-UHFFFAOYSA-N 0.000 claims 1
- 125000000732 arylene group Chemical group 0.000 claims 1
- GDFLGQIOWFLLOC-UHFFFAOYSA-N azane;2-hydroxypropanoic acid;titanium Chemical compound [NH4+].[Ti].CC(O)C([O-])=O GDFLGQIOWFLLOC-UHFFFAOYSA-N 0.000 claims 1
- GOZLPQZIQDBYMO-UHFFFAOYSA-N azanium;zirconium;fluoride Chemical compound [NH4+].[F-].[Zr] GOZLPQZIQDBYMO-UHFFFAOYSA-N 0.000 claims 1
- 239000000440 bentonite Substances 0.000 claims 1
- 229910000278 bentonite Inorganic materials 0.000 claims 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical group O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 claims 1
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- 125000002843 carboxylic acid group Chemical group 0.000 claims 1
- 229910052804 chromium Inorganic materials 0.000 claims 1
- 239000011651 chromium Substances 0.000 claims 1
- 229940064958 chromium citrate Drugs 0.000 claims 1
- 150000001845 chromium compounds Chemical class 0.000 claims 1
- SWXXYWDHQDTFSU-UHFFFAOYSA-K chromium(3+);2-hydroxypropane-1,2,3-tricarboxylate Chemical compound [Cr+3].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O SWXXYWDHQDTFSU-UHFFFAOYSA-K 0.000 claims 1
- QWWLTGUEZNQHMO-UHFFFAOYSA-H chromium(3+);propanedioate Chemical compound [Cr+3].[Cr+3].[O-]C(=O)CC([O-])=O.[O-]C(=O)CC([O-])=O.[O-]C(=O)CC([O-])=O QWWLTGUEZNQHMO-UHFFFAOYSA-H 0.000 claims 1
- PYXSPTLIBJZHQW-UHFFFAOYSA-K chromium(3+);propanoate Chemical compound [Cr+3].CCC([O-])=O.CCC([O-])=O.CCC([O-])=O PYXSPTLIBJZHQW-UHFFFAOYSA-K 0.000 claims 1
- WYYQVWLEPYFFLP-UHFFFAOYSA-K chromium(3+);triacetate Chemical compound [Cr+3].CC([O-])=O.CC([O-])=O.CC([O-])=O WYYQVWLEPYFFLP-UHFFFAOYSA-K 0.000 claims 1
- WIEGKKSLPGLWRN-UHFFFAOYSA-N ethyl 3-oxobutanoate;titanium Chemical compound [Ti].CCOC(=O)CC(C)=O WIEGKKSLPGLWRN-UHFFFAOYSA-N 0.000 claims 1
- 239000004403 ethyl p-hydroxybenzoate Substances 0.000 claims 1
- 235000010228 ethyl p-hydroxybenzoate Nutrition 0.000 claims 1
- 229940043351 ethyl-p-hydroxybenzoate Drugs 0.000 claims 1
- NUVBSKCKDOMJSU-UHFFFAOYSA-N ethylparaben Chemical compound CCOC(=O)C1=CC=C(O)C=C1 NUVBSKCKDOMJSU-UHFFFAOYSA-N 0.000 claims 1
- 239000004312 hexamethylene tetramine Substances 0.000 claims 1
- 235000010299 hexamethylene tetramine Nutrition 0.000 claims 1
- ULULAZKOCFNOIM-UHFFFAOYSA-N hexyl 4-hydroxybenzoate Chemical compound CCCCCCOC(=O)C1=CC=C(O)C=C1 ULULAZKOCFNOIM-UHFFFAOYSA-N 0.000 claims 1
- 229910052742 iron Inorganic materials 0.000 claims 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical group O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims 1
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 claims 1
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 claims 1
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 claims 1
- 229940088644 n,n-dimethylacrylamide Drugs 0.000 claims 1
- YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 claims 1
- YPHQUSNPXDGUHL-UHFFFAOYSA-N n-methylprop-2-enamide Chemical compound CNC(=O)C=C YPHQUSNPXDGUHL-UHFFFAOYSA-N 0.000 claims 1
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 claims 1
- 229920002866 paraformaldehyde Polymers 0.000 claims 1
- 150000002989 phenols Chemical class 0.000 claims 1
- DYUMLJSJISTVPV-UHFFFAOYSA-N phenyl propanoate Chemical compound CCC(=O)OC1=CC=CC=C1 DYUMLJSJISTVPV-UHFFFAOYSA-N 0.000 claims 1
- 229960000969 phenyl salicylate Drugs 0.000 claims 1
- 229940049953 phenylacetate Drugs 0.000 claims 1
- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 claims 1
- 229950009215 phenylbutanoic acid Drugs 0.000 claims 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 claims 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims 1
- 150000003254 radicals Chemical class 0.000 claims 1
- 229960001755 resorcinol Drugs 0.000 claims 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 claims 1
- 229960004889 salicylic acid Drugs 0.000 claims 1
- 239000012266 salt solution Substances 0.000 claims 1
- 125000005649 substituted arylene group Chemical group 0.000 claims 1
- BUUPQKDIAURBJP-UHFFFAOYSA-N sulfinic acid Chemical compound OS=O BUUPQKDIAURBJP-UHFFFAOYSA-N 0.000 claims 1
- KUCOHFSKRZZVRO-UHFFFAOYSA-N terephthalaldehyde Chemical compound O=CC1=CC=C(C=O)C=C1 KUCOHFSKRZZVRO-UHFFFAOYSA-N 0.000 claims 1
- 229910052719 titanium Inorganic materials 0.000 claims 1
- 239000010936 titanium Substances 0.000 claims 1
- 150000003609 titanium compounds Chemical class 0.000 claims 1
- 229920003169 water-soluble polymer Polymers 0.000 claims 1
- 150000003755 zirconium compounds Chemical class 0.000 claims 1
- XJUNLJFOHNHSAR-UHFFFAOYSA-J zirconium(4+);dicarbonate Chemical compound [Zr+4].[O-]C([O-])=O.[O-]C([O-])=O XJUNLJFOHNHSAR-UHFFFAOYSA-J 0.000 claims 1
Classifications
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- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/182—Radicals derived from carboxylic acids
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- C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
- C07C237/04—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated
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- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
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- C08F26/02—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen by a single or double bond to nitrogen
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Claims (12)
1. Anvendelse av en sammensetning som omfatter en polymer som omfatter repeterende enheter avledet, fra en nitrogen-inneholdende olefinisk monomer som har formelen
eller en kombinasjon derav med minst en ytterligere nitrogen-inneholdende olefinisk forbindelse som har formelen valgt fra
hvor Ri og R2 er de samme eller forskjellige og hver uavhengig valgt fra hydrogen, alkylradikal, arylradikal, arylalkylradikal, alkarylradikal og kombinasjoner av hvilke som helst av to eller flere av disse hvor hvert radikal inneholder 1-30 karbonatomer;
M er en substituert eller usubstituert morfolingruppe;
hver Y er uavhengig valgt fra alkylenradikal, fenylgruppe, imidazoliumgruppe, naftylgruppé, bifenylgruppe og kombinasjoner av hvilke som helst av to eller flere avdisse;
hver X er et anion valgt fra halogenid, sulfat, fosfat, nitrat, sulfonatj fosfonater, sulfinat, fosfinat og kombinasjoner av hvilke som helst av to eller flere av disse;
Ar er en arylengruppe; og
hver m er uavhengig 0 eller 1;
i en underjordisk formasjon. "
2. Anvendelse ifølge krav 1,
hvor polymeren ytterligere omfatter repeterende enheter avledet fra minst én olefinisk komonomer med formelen valgt fra
og kombinasjoner av hvilke som helst av to eller flere av disse, hvor hver R\ og R2 er de samme eller forskjellige og er uavhengig valgt fra hydrogen, alkylradikal, arylradikal, aralkylradikal, alkarylradikal og kombinasjoner av hvilke som helst av to eller flere av disse;
hver m er uavhengig 0 eller 1;
Z har formelen valgt fra N(R2)(R2), N<+>(R2)(R2)(R2)X" hvor X er et anion valgt fra halogenid, sulfat, fosfat, nitrat, sulfonat, fosfonater, sulfinat, fosfinat og kombinasjoner av hvilke som helst av to eller flere av disse;
G er N(R,), N(R2) eller O;
h<y>er Y er uavhengig valgt fra alkylenradikal, fenylgruppe, imidazoliumgruppe, naftylgruppe, bifenylgruppe og kombinasjoner av to eller flere av disse; og W er en syreandel valgt fra fosfinsyre, fosfonsyre, sulfinsyre, sulfonsyre,
svovelsyre, svovelsyrling, karboksylsyre, fosforsyre, ammoniumsalt eller alkalimetallsalt av hvilke som helst av disse syrer, og kombinasjoner av hvilke som helst av to eller flere av disse.
3. Anvendelse ifølge krav i eller 2,
hvor den nitrogen-inneholdende olefiniske monomer er valgt fra N-(2-amino-2-oksoetyl)-N'-vinyl imidazoliumklorid, N-(3-amino-3-oksopropyl)-N'-vinyl imidazoliumklorid, og N-(4-amino-4-oksobutyl)-N'-vinyl imidazoliumklorid, eller en kombinasjon derav med minst én ytterligere nitrogen-inneholdende olefinisk monomer valgt fra N-akryloyl morfolin, N-akryloyl-N'-metyl piperazin,
N-akryloyl-N'-etyl piperazin, N-akryloyl-N'-propy] piperazin, N-akryloyl-N'-(3-sulfopropyl)-N'-metyl piperazinium inner salt, N-akryloyl-N'-(3-sulfopropyl)-N'-etyl piperazinium inner salt, N-akryloyl-N'-(3-sulfopropyl)-N'-metyl piperazinium inner salt, N-akryloyl-N'-(3-sulfopropyl)-N'-etyl piperazinium inner salt, N-akryloyl-N'-(2-amino-2-oksoetyl)-N'-metyl piperaziniumklorid, N-akryloyl-N'-(3-amino-3-oksopropyl)-N'-metyl piperaziniumklorid, N-akryloyl-N'-(4-amino-4-oksobutyl)-N'-metyl piperaziniumklorid, N-akryloyl-N'-(2-amino-2-oksoetyl)-N'-etyl piperaziniumklorid, N-akryloyl-N'-(3-amino-3-oksopropyl)-N'-etyl piperaziniumklorid, N-akryloyl-N'-(4-amino-4-oksobutyl)-N'-etyl piperaziniumklorid, N,N-dimetyl-N-(3-sulfopropyl)-N-(4-vinylbenzyl) ammonium inner salt,
N,N-dimetyl-N-(4-sulfobutyl)-N-(4-vinylbenzyl) ammonium inner salt, N,N-dietyl-N-(3-sulfopropyl)-N-(4-vinylbenzyl) ammonium inner salt, N,N-dietyl-N-(4-sulfobutyl)-N-(4-vinylbenzyl) ammonium inner salt, N,N-dimetyl-N-(3-sulfopropyl)-N-(3-vinylbenzyl) ammonium inner salt, N,N-dimetyl-N-(4-sulfobutyl)-N-(3-vinylbenzyl) ammonium inner salt, N,N-dietyl-N-(3-sulfopropyl)-N-(3-vinylbenzyl) ammonium inner salt, N,N-dietyl-N-(4-sulfqbutyl)-N-(3-vinylbenzyl) ammonium inner salt, N,N-dimetyl-N-(2-amino-2-oksoetyl)-N-(4-yinylbenzyl) ammoniumklorid, N,N-dietyl-N-(2-åmino-2-oksoetyl)-N-(4-vinylbenzyl) ammoniumklorid, N,N-dimetyl-N-(3-amino-3-oksopropyl)-N-(4-vinylbenzyl) ammoniumklorid, N,N-dietyl-N-(3-aminb-3-oksopropyl)-N-(4-vinylbenzyl) ammoniumklorid, N,N-dimetyl-N-(2-amino-2-oksoetyl)-N-(3-vinylbenzyl) ammoniumklorid, N,N-dietyl-N-(2-amino-2-oksoetyl)-N-(3-vinylbenzyl) ammoniumklorid, N,N-dimetyl-N-(3-amino-3-oksopropyl)-N-(3-vinylbenzyl) ammoniumklorid, N,N-dietyl-N-(3-amino-3-oksopropyl)-N-(3-vinylbenzyl) ammoniumklorid, N,N-dimetyl-N-(3- sul fopropyl)-3-(akryl oylamino)-1 -propanammonium inner salt, N,N-dietyl-N-(3-sulfopropyl)-3-(akryloylamino)-1 -propanammonium inner salt, N,N-dimetyl-N-(3-sulfobutyl)-3-(akryloylamino)-1 -propanammonium inner salt, N,N-dietyl-N-(4-sulfobutyl)-3-(akryloylamino)-1 -propanammonium inner salt, N,N-dimetyl-N-(3-sulfopropyl)-2-(akryloylamino)-l-etanammonium inner salt, N,N-dietyl-N-(3-sulfopropyl)-2-(akrylOyIamino)-l-etanammonium inner salt, og N,N-dimetyl-N-(4-sulfobutyl)-2-akryloylamino)-1 -etanammonium inner salt.
4. Anvendelse ifølge hvilke som helst av kravene 1-3,
hvor den nitrogen-inneholdende olefiniske monomeren er valgt fra N-(2-amino-2-bksoetyl)-N'-vinylimidazoliumklorid, N-(3-amino-3-oksopropyl)-N<*->vinylimidazoliumklorid, N-(4-amino-4-oksobutyl)-N<*->vinylimidazoliumklorid eller en kombinasjon derav med minst én ytterligere nitrogen-inneholdende olefinisk forbindelse valgt fra N,N-dimetyl-N-(3-sulfopropyl)-N-(4-vinylbenzyl) ammonium inner salt, N,N-dimetyl-N-(3-sulfobutyl)-N-(4-vinylbenzyl) ammonium inner salt, N,N-dietyl-N-(3-sulfopropyl)-N-(4-vinylbenzyl) ammonium' inner salt, N,N-dietyl-N-(3-sulfobutyl)-N-(4-vinylbenzyl) ammonium inner salt, N,N-dimetyl-N-(3-sulfopropyl)-N-(3-vinylbenzyl) ammonium inner salt, N,N-dimetyl-N-(3-sulfobutyl)-N-(3-vinylbenzyl) ammonium inner salt,. N,N-dietyl-N-(3-sulfopropyl)-N-(3-vinylbenzyl) ammonium inner salt, N,N-dietyl-N-(3-sulfobutyl)-N-(3-vinylbenzyl) ammonium inner salt, N-akryloyl-N<*->metyl-N<*->(2-amino-2-oksoetyl) piperaziniumklorid, N-akryloyl-N'-metyl-N'-(3-amino-3-oksopropyl) piperaziniumklorid, N-akryloyl-N'-metyl-N'-(4-amino-4-oksobutyl) piperaziniumklorid, N-akryloy-N<*->etyl-N'-(2-amino-2-oksoetyl) piperaziniumklorid, N-akrylovl-N'-etvl-N'-(3-amino-3-oksoDroovn oioeraziniumklorid.
N-akryloyl-N'-etyl-N'-(4-amino-4-oksobutyl) piperaziniumklorid, N,N-dimetyl-N-(2-amino-2-oksoetyl)-N-(4-vinylbenzyl) ammoniumklorid, N,N-dietyl-N-(2-amino-2-oksoetyl)-N-(4-vinylbenzyl) ammoniumklorid, N,N-dimetyl-N^(3-amino-3-oksopropyl)-N-(4-vinylbenzyl) ammoniumklorid, og N,N-dietyl-N-(3-amino-3-oksopropyl)-N-(4-vinylbenzyl) ammoniumklorid.
5. Anvendelse ifølge hvilket som helst av kravene 1-4,
hvor den ytterligere nitrogen-inneholdende olefiniske monomer er N-akryloyl-N'-metyl piperazin, N-akryloyl-N'-(3-sulfopropyl)-N'-metyl piperazinium inner salt, N-akryloyl-N'-(2-amino-2-oksoetyl)-N'-metyl piperaziniumklorid, N,N-dimetyl-N-(3-sulfopropyl)-N-(4-vinylbenzyl) ammonium inner salt, N,N-dimetyl-N-(2-amino-2-oksoetyl)-N-(4-vinylbenzyl) ammoniumklorid, N,N-dimetyl-N-(3-sulfopropyl)-3-(akryloylamino)-1 -propanammonium inner salt, eller N-akryloylmorfolin.
6. Anvendelse ifølge hvilket som helst av kravene 2-5,
hvor den olefiniske komonomeren ér valgt fra akrylamid, styrensulfonsyre, salt av styrensulfonsyre, N-metylakrylamid, N,N-dimetylakrylamid, akrylsyre, salt av akrylsyre, N-vinylpyrrolidon, metylakrylat, metakrylat, vinylsulfonsyre, salt av vinylsulfonsyre, 2-åkryl-amido-2-metylpropansulfonsyre, salt av 2-akrylamido-2-metylpropansulfonsyre, fortrinnsvis kombinasjoner av hvilke som helst av to eller flere av disse, særlig hvor den olefiniske komonomer er akrylamid.
7. Anvendelse av en sammensetning som omfatter en vannoppløselig polymer, et tverrbindingsmiddel og en væske, hvor polymeren er som angitt i hvilket som helst av krav 1-6, i en underjordisk formasjon.
8. Anvendelse ifølge krav 7,
hvor tverrbindingsmidlet er en flerverdig metallforbindelse hvor metallet av metallforbindelsen er valgt fra Zr, Al, Cr, Fe, Ti og kombinasjoner av hvilke som helst av to' eller flere av disse.
9. Anvendelse ifølge krav 7,
hvor tverrbindingsmidlet er valgt fra en zirkoniumforbindelse, en titanforbindelse, en kromforbindelse, en aluminiumforbindelse, og kombinasjoner av hvilke som helst av to eller flere av disse, særlig fra zirkoniumcitrat, zirkoniumkompleks av hydroksyetylglycin, ammoniumzirkoniumfluorid, zirkonium 2-etylheksanoat, zirkoniumacetat, zirkoniumneodekanoat, zirkoniumacetylacetonat, tetrakis(trietanolamin)zirkonat, zirkoniumkarbonat, ammoniumzirkoniumkarbonat, zirkonylammoniumkarbonat, zirkoniumlaktat, titanacetylacetonat, titanetylacetoacetat, titancitrat, titantrietanolamin, ammoniumtitanlaktat, aluminiumcitrat, kromcitrat, kromacetat, krompropionat, krommalonat, og kombinasjoner av hvilke som helst av to eller flere av disse.
10. Anvendelse ifølge krav 7,
hvor tverrbindingsmidlet omfatter to komponenter hvor den første komponenten er valgt fra fenol, substituerte fenoler, aspirin, p-aminobenzosyre, resorcinol, katekol, hydrokinon, furfurylalkohol, R'ArO(C=0)mR', HOAr(C=0)mOR', HOArOH, R'OArOH, R'OArOR\ eller kombinasjoner av hvilke som helst av to eller flere av disse, hvor Ar er ikke-substituert eller substituert arylengruppe, hver R' kan være den samme eller kan være forskjellig og er hver uavhengig valgt fra hydrogen, karboksylsyregruppe, en Cj-C6-alkyl, en fenylgruppe eller kombinasjoner av hvilke som helst av to eller flere av disse, og hver m er uavhengig 0 eller 1; og den andre komponenten er valgt fra aldehyder, aldehydgenerérende forbindelser, og kombinasjoner av hvilke som helst av to eller flere av disse, særlig hvor den første komponenten er valgt fra fenol, hydrokinon, resorcinol, katekol, p-aminosalicylsyre, furfurlalkohol, fenylacetat, fenylpropionat, fenylbutyrat, salicylsyre, fenylsalicylat, aspirin, p-hydroksybenzosyre, metyl p-hydroksybenzoat, metyl p-aminobenzosyre, o-hydroksybenzoat, etyl p-hydroksybenzoat, o-hydroksybenzosyre, heksyl p-hydroksybenzoat, og kombinasjoner av hvilke som helst av to eller flere av disse; og den andre komponenten er valgt fra formaldehyd, paraformaldehyd, acetaldehyd, propionaldehyd, dekanal, glutaraldehyd, tereftaldehyd, heksametylentetramin, og kombinasjoner av hvilke som helst av to eller flere av disse.
11. Anvendelse ifølge krav 7,
hvor væsken er en produsert saltoppløsning.
12. Anvendelse av en sammensetning som omfatter en leire, polymer og en væske, hvor polymeren er som angitt i hvilket som helst av krav 1-6, i en underjordisk formasjon; særlig hvor leiren er bentonitt.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/575,429 US5708107A (en) | 1995-12-20 | 1995-12-20 | Compositions and processes for treating subterranean formations |
US08/575,928 US5650633A (en) | 1995-12-20 | 1995-12-20 | Compositions and processes for treating subterranean formations |
US08/575,434 US6051670A (en) | 1995-12-20 | 1995-12-20 | Compositions and processes for treating subterranean formations |
US08/723,635 US5922653A (en) | 1995-12-20 | 1996-10-03 | Compositions and processes for treating subterranean formations |
PCT/US1996/018174 WO1997022638A1 (en) | 1995-12-20 | 1996-11-13 | Compositions and processes for treating subterranean formations |
Publications (3)
Publication Number | Publication Date |
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NO982888D0 NO982888D0 (no) | 1998-06-19 |
NO982888L NO982888L (no) | 1998-08-20 |
NO322844B1 true NO322844B1 (no) | 2006-12-11 |
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NO19982888A NO322844B1 (no) | 1995-12-20 | 1998-06-19 | Anvendelse av en sammensetning i en underjordisk formasjon. |
NO20054619A NO20054619D0 (no) | 1995-12-20 | 2005-10-07 | Sammensetninger og fremgangsmater for behandling av underjordiske formasjoner |
Family Applications After (1)
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NO20054619A NO20054619D0 (no) | 1995-12-20 | 2005-10-07 | Sammensetninger og fremgangsmater for behandling av underjordiske formasjoner |
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AU (1) | AU719976B2 (no) |
CA (1) | CA2241362C (no) |
GB (3) | GB2340496B (no) |
MX (1) | MX9804985A (no) |
NO (2) | NO322844B1 (no) |
WO (1) | WO1997022638A1 (no) |
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DE102007059844A1 (de) * | 2007-12-12 | 2009-06-25 | Basf Construction Polymers Gmbh | Copolymer auf Basis einer Sulfonsäure-haltigen Verbindung |
FR2986034B1 (fr) | 2012-01-20 | 2016-08-12 | Snf Sas | Procede de recuperation assistee de petrole par injection d'une solution polymerique |
FR2986033B1 (fr) | 2012-01-20 | 2016-08-05 | Snf Sas | Procede de recuperation assistee de petrole par injection d'une solution polymerique |
CN111454709B (zh) * | 2019-01-21 | 2022-06-24 | 中国石油化工股份有限公司 | 海水基酸液体系 |
CN110776595B (zh) * | 2019-10-17 | 2021-09-21 | 中国石油天然气股份有限公司 | 一种驱油用线性抗盐聚合物及其制备方法 |
US11685852B2 (en) * | 2020-09-03 | 2023-06-27 | Aramco Services Company | Reservoir drilling fluids consist of cationic heterocyclic polymers, synthesis, formulation, and applications |
CN114213584B (zh) * | 2021-12-24 | 2023-05-26 | 西南石油大学 | 离子液体聚合物、其制备方法及其应用、抑制剂及其应用 |
CN116535587B (zh) * | 2023-06-13 | 2023-10-27 | 石家庄华莱鼎盛科技有限公司 | 钻井液用天然植物多酚改性酚醛树脂降滤失剂 |
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DE1266898B (de) * | 1961-04-15 | 1968-04-25 | Basf Ag | Verfahren zur Herstellung von Farbstoffen der Azo-, Anthrachinon- und Phthalocyaninreihe |
GB1221820A (en) * | 1967-05-12 | 1971-02-10 | Basf Ag | Basic azo dyes |
CH645653A5 (de) * | 1980-08-01 | 1984-10-15 | Ciba Geigy Ag | Quaternaere, copolymere, hochmolekulare ammoniumsalze auf acrylbasis, deren herstellung und verwendung als aktive komponente in kosmetischen mitteln. |
OA08092A (fr) * | 1984-05-11 | 1987-03-31 | Bristol Myers Co | Novel bile sequestrant resin and uses. |
JPH0788505B2 (ja) * | 1986-06-02 | 1995-09-27 | 三井東圧化学株式会社 | 石油三次回収薬剤 |
US5384232A (en) * | 1991-12-02 | 1995-01-24 | E. I. Du Pont De Nemours And Company | Process for rapid access development of silver halide films using pyridinium as development accelerators |
JP3066159B2 (ja) * | 1991-12-27 | 2000-07-17 | 株式会社クラレ | ハードコート形成用組成物 |
US5270382A (en) * | 1992-04-24 | 1993-12-14 | Phillips Petroleum Company | Compositions and applications thereof of water-soluble copolymers comprising an ampholytic imidazolium inner salt |
US5250642A (en) * | 1992-05-20 | 1993-10-05 | Phillips Petroleum Company | Copolymers of ampholytic ion pairs containing vinylic tertiary amine and olefinic comonomers |
US5378842A (en) * | 1993-12-21 | 1995-01-03 | E. I. Du Pont De Nemours And Company | Imidazolium hardeners for proteinaceous materials |
JPH07258202A (ja) * | 1994-03-18 | 1995-10-09 | Nippon Oil & Fats Co Ltd | 重合性ベタイン化合物 |
JPH07258342A (ja) * | 1994-03-22 | 1995-10-09 | Toyobo Co Ltd | 耐塩水性ラテックス |
JPH07300513A (ja) * | 1994-05-09 | 1995-11-14 | Nippon Oil & Fats Co Ltd | 表面グラフト化材料 |
US5563214A (en) * | 1994-08-09 | 1996-10-08 | Henkel Corporation | Aqueous compositions containing polymerizable surfactant compounds |
-
1996
- 1996-11-13 WO PCT/US1996/018174 patent/WO1997022638A1/en active Application Filing
- 1996-11-13 AU AU77297/96A patent/AU719976B2/en not_active Expired
- 1996-11-13 GB GB9930053A patent/GB2340496B/en not_active Expired - Lifetime
- 1996-11-13 GB GB9926318A patent/GB2340832B/en not_active Expired - Lifetime
- 1996-11-13 CA CA002241362A patent/CA2241362C/en not_active Expired - Lifetime
- 1996-11-13 GB GB9813343A patent/GB2324095B/en not_active Expired - Lifetime
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1998
- 1998-06-19 NO NO19982888A patent/NO322844B1/no not_active IP Right Cessation
- 1998-06-19 MX MX9804985A patent/MX9804985A/es active IP Right Grant
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Also Published As
Publication number | Publication date |
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GB2340832A (en) | 2000-03-01 |
GB2324095A (en) | 1998-10-14 |
WO1997022638A1 (en) | 1997-06-26 |
AU7729796A (en) | 1997-07-14 |
GB2340496A (en) | 2000-02-23 |
GB9926318D0 (en) | 2000-01-12 |
GB2324095B (en) | 2000-05-17 |
NO20054619D0 (no) | 2005-10-07 |
NO982888D0 (no) | 1998-06-19 |
GB9813343D0 (en) | 1998-08-19 |
GB9930053D0 (en) | 2000-02-09 |
GB2340496B (en) | 2000-05-17 |
NO982888L (no) | 1998-08-20 |
NO20054619L (no) | 1998-08-20 |
AU719976B2 (en) | 2000-05-18 |
CA2241362A1 (en) | 1997-06-26 |
GB2340832B (en) | 2000-05-10 |
CA2241362C (en) | 2005-03-29 |
MX9804985A (es) | 1998-09-30 |
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