EA000794B1 - Аминосилановые соли и силаноамиды карбоновых кислот как ингибиторы коррозии - Google Patents
Аминосилановые соли и силаноамиды карбоновых кислот как ингибиторы коррозии Download PDFInfo
- Publication number
- EA000794B1 EA000794B1 EA199800091A EA199800091A EA000794B1 EA 000794 B1 EA000794 B1 EA 000794B1 EA 199800091 A EA199800091 A EA 199800091A EA 199800091 A EA199800091 A EA 199800091A EA 000794 B1 EA000794 B1 EA 000794B1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- alkyl
- oxygen
- alkoxy
- interrupted
- unsubstituted
- Prior art date
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- 238000005260 corrosion Methods 0.000 title claims abstract description 65
- 230000007797 corrosion Effects 0.000 title claims abstract description 62
- 239000003112 inhibitor Substances 0.000 title claims abstract description 58
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical class [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 title claims abstract description 48
- 150000001735 carboxylic acids Chemical class 0.000 title claims abstract description 13
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 205
- 239000001257 hydrogen Substances 0.000 claims abstract description 192
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 192
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 186
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 183
- 239000001301 oxygen Substances 0.000 claims abstract description 182
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 149
- -1 naphthoxy Chemical group 0.000 claims abstract description 149
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 132
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 130
- 239000011593 sulfur Substances 0.000 claims abstract description 130
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 128
- 150000002431 hydrogen Chemical group 0.000 claims abstract description 104
- 150000003839 salts Chemical class 0.000 claims abstract description 82
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 78
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 73
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 71
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 67
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 57
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 56
- 239000008199 coating composition Substances 0.000 claims abstract description 55
- 150000001721 carbon Chemical group 0.000 claims abstract description 54
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 48
- 125000001624 naphthyl group Chemical group 0.000 claims abstract description 41
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 41
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 40
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 35
- 150000002367 halogens Chemical group 0.000 claims abstract description 35
- 229920002125 Sokalan® Polymers 0.000 claims abstract description 34
- 150000001408 amides Chemical class 0.000 claims abstract description 33
- 125000003884 phenylalkyl group Chemical group 0.000 claims abstract description 33
- 239000004584 polyacrylic acid Substances 0.000 claims abstract description 32
- 229920001577 copolymer Polymers 0.000 claims abstract description 31
- 239000000460 chlorine Chemical group 0.000 claims abstract description 27
- 125000002993 cycloalkylene group Chemical group 0.000 claims abstract description 27
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 25
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 25
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 24
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims abstract description 23
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 23
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 20
- 125000004414 alkyl thio group Chemical group 0.000 claims abstract description 19
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 19
- 125000000392 cycloalkenyl group Chemical group 0.000 claims abstract description 17
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims abstract description 16
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims abstract description 16
- 125000001118 alkylidene group Chemical group 0.000 claims abstract description 16
- 125000006710 (C2-C12) alkenyl group Chemical group 0.000 claims abstract description 14
- 125000004450 alkenylene group Chemical group 0.000 claims abstract description 14
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims abstract description 14
- 125000001188 haloalkyl group Chemical group 0.000 claims abstract description 13
- 125000004419 alkynylene group Chemical group 0.000 claims abstract description 11
- 125000004957 naphthylene group Chemical group 0.000 claims abstract description 11
- 125000006702 (C1-C18) alkyl group Chemical group 0.000 claims abstract description 10
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 10
- 125000000081 (C5-C8) cycloalkenyl group Chemical group 0.000 claims abstract description 8
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims abstract description 8
- 125000005592 polycycloalkyl group Polymers 0.000 claims abstract description 8
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims abstract description 7
- 125000002071 phenylalkoxy group Chemical group 0.000 claims abstract description 6
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims abstract description 5
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims abstract 5
- 125000004434 sulfur atom Chemical group 0.000 claims description 62
- 239000000203 mixture Substances 0.000 claims description 57
- 238000000576 coating method Methods 0.000 claims description 53
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 49
- 239000011248 coating agent Substances 0.000 claims description 49
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 claims description 40
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 33
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 30
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 26
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 26
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 26
- 239000011976 maleic acid Substances 0.000 claims description 26
- 229910052751 metal Inorganic materials 0.000 claims description 26
- 239000002184 metal Substances 0.000 claims description 26
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 26
- 239000003795 chemical substances by application Substances 0.000 claims description 23
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 23
- 239000000463 material Substances 0.000 claims description 22
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 claims description 20
- 239000000126 substance Substances 0.000 claims description 19
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 16
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 15
- 229910052757 nitrogen Inorganic materials 0.000 claims description 14
- 239000007787 solid Substances 0.000 claims description 14
- 125000001326 naphthylalkyl group Chemical group 0.000 claims description 13
- 239000000049 pigment Substances 0.000 claims description 13
- 238000001035 drying Methods 0.000 claims description 11
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 10
- 229920000647 polyepoxide Polymers 0.000 claims description 9
- MALIONKMKPITBV-UHFFFAOYSA-N 2-(3-chloro-4-hydroxyphenyl)-n-[2-(4-sulfamoylphenyl)ethyl]acetamide Chemical compound C1=CC(S(=O)(=O)N)=CC=C1CCNC(=O)CC1=CC=C(O)C(Cl)=C1 MALIONKMKPITBV-UHFFFAOYSA-N 0.000 claims description 8
- 239000003822 epoxy resin Substances 0.000 claims description 8
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- 229920000178 Acrylic resin Polymers 0.000 claims description 6
- 239000004925 Acrylic resin Substances 0.000 claims description 6
- 125000004956 cyclohexylene group Chemical group 0.000 claims description 6
- 239000000945 filler Substances 0.000 claims description 6
- 239000005011 phenolic resin Substances 0.000 claims description 6
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 claims description 5
- XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 claims description 5
- 239000002318 adhesion promoter Substances 0.000 claims description 5
- 230000032683 aging Effects 0.000 claims description 5
- 229920000180 alkyd Polymers 0.000 claims description 5
- 238000011065 in-situ storage Methods 0.000 claims description 5
- 229920005749 polyurethane resin Polymers 0.000 claims description 5
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 4
- 239000002270 dispersing agent Substances 0.000 claims description 4
- 239000000975 dye Substances 0.000 claims description 4
- GJVFBWCTGUSGDD-UHFFFAOYSA-L pentamethonium bromide Chemical compound [Br-].[Br-].C[N+](C)(C)CCCCC[N+](C)(C)C GJVFBWCTGUSGDD-UHFFFAOYSA-L 0.000 claims description 4
- 230000001681 protective effect Effects 0.000 claims description 4
- 239000000758 substrate Substances 0.000 claims description 4
- 239000013008 thixotropic agent Substances 0.000 claims description 4
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- 229920001225 polyester resin Polymers 0.000 claims description 3
- 239000004645 polyester resin Substances 0.000 claims description 3
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 3
- 229910052720 vanadium Inorganic materials 0.000 claims description 3
- 229920006243 acrylic copolymer Polymers 0.000 claims description 2
- 239000003963 antioxidant agent Substances 0.000 claims description 2
- 239000003054 catalyst Substances 0.000 claims description 2
- 238000011156 evaluation Methods 0.000 claims description 2
- 239000004611 light stabiliser Substances 0.000 claims description 2
- HVZWVEKIQMJYIK-UHFFFAOYSA-N nitryl chloride Chemical group [O-][N+](Cl)=O HVZWVEKIQMJYIK-UHFFFAOYSA-N 0.000 claims description 2
- YDZNRNHKJQTGCG-UHFFFAOYSA-N 1,1'-binaphthyl-2,2'-dicarboxylic acid Chemical compound C1=CC=C2C(C3=C4C=CC=CC4=CC=C3C(=O)O)=C(C(O)=O)C=CC2=C1 YDZNRNHKJQTGCG-UHFFFAOYSA-N 0.000 claims 11
- 239000011230 binding agent Substances 0.000 abstract description 5
- NFGODEMQGQNUKK-UHFFFAOYSA-M [6-(diethylamino)-9-(2-octadecoxycarbonylphenyl)xanthen-3-ylidene]-diethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCCOC(=O)C1=CC=CC=C1C1=C2C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C21 NFGODEMQGQNUKK-UHFFFAOYSA-M 0.000 abstract description 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- 125000005605 benzo group Chemical class 0.000 abstract 2
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 abstract 1
- 125000004846 (C1-C4) allyl group Chemical group 0.000 abstract 1
- KCNKJCHARANTIP-SNAWJCMRSA-N allyl-{4-[3-(4-bromo-phenyl)-benzofuran-6-yloxy]-but-2-enyl}-methyl-amine Chemical compound C=1OC2=CC(OC/C=C/CN(CC=C)C)=CC=C2C=1C1=CC=C(Br)C=C1 KCNKJCHARANTIP-SNAWJCMRSA-N 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 72
- 150000001875 compounds Chemical class 0.000 description 67
- 150000003254 radicals Chemical class 0.000 description 54
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 50
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 35
- 238000003756 stirring Methods 0.000 description 31
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 28
- 238000012360 testing method Methods 0.000 description 27
- 239000005639 Lauric acid Substances 0.000 description 25
- 239000000243 solution Substances 0.000 description 23
- 238000006277 sulfonation reaction Methods 0.000 description 14
- 230000032798 delamination Effects 0.000 description 13
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- 239000002253 acid Substances 0.000 description 12
- 239000006185 dispersion Substances 0.000 description 12
- 239000007921 spray Substances 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 239000012299 nitrogen atmosphere Substances 0.000 description 11
- 229920005989 resin Polymers 0.000 description 11
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- 229910000831 Steel Inorganic materials 0.000 description 9
- 238000002360 preparation method Methods 0.000 description 9
- 239000010959 steel Substances 0.000 description 9
- 239000007788 liquid Substances 0.000 description 8
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 7
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 6
- 239000004593 Epoxy Substances 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 6
- 239000007888 film coating Substances 0.000 description 6
- 238000009501 film coating Methods 0.000 description 6
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- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 6
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 6
- 238000005507 spraying Methods 0.000 description 6
- BVWMLPXXYGTRHW-UHFFFAOYSA-N 3-(4,6,11-trioxa-1-aza-5-silabicyclo[3.3.3]undecan-5-yl)propan-1-amine Chemical compound O1CCN2CCO[Si]1(CCCN)OCC2 BVWMLPXXYGTRHW-UHFFFAOYSA-N 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 5
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 5
- 238000000227 grinding Methods 0.000 description 5
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
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- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 4
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- 150000007513 acids Chemical class 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
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- 125000006832 (C1-C10) alkylene group Chemical group 0.000 description 3
- GOBWHQOQBVSUEI-UHFFFAOYSA-N 2-(3-aminopropylsilyloxy)ethane-1,1-diol Chemical compound NCCC[SiH2]OCC(O)O GOBWHQOQBVSUEI-UHFFFAOYSA-N 0.000 description 3
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- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 3
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- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
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- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 3
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- JSYPRLVDJYQMAI-ODZAUARKSA-N (z)-but-2-enedioic acid;prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)\C=C/C(O)=O JSYPRLVDJYQMAI-ODZAUARKSA-N 0.000 description 2
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 2
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 2
- JNIHETDSIZRHLI-UHFFFAOYSA-N 2-(2-sulfanylidene-3h-1,3-benzothiazol-4-yl)butanedioic acid Chemical compound OC(=O)CC(C(O)=O)C1=CC=CC2=C1NC(=S)S2 JNIHETDSIZRHLI-UHFFFAOYSA-N 0.000 description 2
- IKCLCGXPQILATA-UHFFFAOYSA-N 2-chlorobenzoic acid Chemical compound OC(=O)C1=CC=CC=C1Cl IKCLCGXPQILATA-UHFFFAOYSA-N 0.000 description 2
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Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/08—Anti-corrosive paints
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/08—Anti-corrosive paints
- C09D5/082—Anti-corrosive paints characterised by the anti-corrosive pigment
- C09D5/086—Organic or non-macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/42—Introducing metal atoms or metal-containing groups
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
- C23F11/08—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
- C23F11/10—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
- C23F11/14—Nitrogen-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
- C23F11/08—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
- C23F11/10—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
- C23F11/173—Macromolecular compounds
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Wood Science & Technology (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Paints Or Removers (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
- Anti-Oxidant Or Stabilizer Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH191195 | 1995-06-29 | ||
| PCT/EP1996/002600 WO1997001606A1 (en) | 1995-06-29 | 1996-06-17 | Aminosilane salts and silanamides of carboxylic acids as corrosion inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EA199800091A1 EA199800091A1 (ru) | 1998-08-27 |
| EA000794B1 true EA000794B1 (ru) | 2000-04-24 |
Family
ID=4221483
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA199800091A EA000794B1 (ru) | 1995-06-29 | 1996-06-17 | Аминосилановые соли и силаноамиды карбоновых кислот как ингибиторы коррозии |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US5879436A (enExample) |
| EP (1) | EP0835289B1 (enExample) |
| JP (1) | JPH11508927A (enExample) |
| KR (1) | KR19990028652A (enExample) |
| CN (1) | CN1117825C (enExample) |
| AT (1) | ATE180269T1 (enExample) |
| AU (1) | AU699265B2 (enExample) |
| BR (1) | BR9609321A (enExample) |
| CA (1) | CA2221776A1 (enExample) |
| DE (1) | DE69602530T2 (enExample) |
| DK (1) | DK0835289T3 (enExample) |
| EA (1) | EA000794B1 (enExample) |
| ES (1) | ES2133972T3 (enExample) |
| MX (1) | MX9710433A (enExample) |
| MY (1) | MY129135A (enExample) |
| SG (1) | SG43378A1 (enExample) |
| TW (1) | TW428018B (enExample) |
| WO (1) | WO1997001606A1 (enExample) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| RU2604241C2 (ru) * | 2013-02-19 | 2016-12-10 | Александр Валерьевич Бояринцев | Высокотехнологичное антикоррозийное теплоизоляционное покрытие с повышенными теплотехническими характеристиками |
| RU2625382C1 (ru) * | 2016-06-15 | 2017-07-13 | Общество с ограниченной ответственностью "Центр коррозионных испытаний" (ООО "Центр коррозионных испытаний") | Ингибитор коррозии и коррозионного растрескивания под напряжением |
| RU2676608C1 (ru) * | 2017-10-04 | 2019-01-09 | Общество С Ограниченной Ответственностью "Рустек" | Лакокрасочная композиция для получения тонких покрытий методом катодного электроосаждения |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1082272B1 (en) * | 1998-05-28 | 2001-11-21 | Owens Corning | Corrosion inhibiting composition for polyacrylic acid based binders |
| US6087415A (en) * | 1998-06-11 | 2000-07-11 | Johnson & Johnson Vision Care, Inc. | Biomedical devices with hydrophilic coatings |
| US6500481B1 (en) | 1998-06-11 | 2002-12-31 | Johnson & Johnson Vision Care, Inc. | Biomedical devices with amid-containing coatings |
| RU2157397C1 (ru) * | 1999-10-18 | 2000-10-10 | Общество с ограниченной ответственностью "Элкон" | Композиция для защитного покрытия |
| RU2182582C2 (ru) * | 1999-12-23 | 2002-05-20 | Открытое акционерное общество "Химпром" | Композиция для термостойкого антикоррозионного покрытия |
| US6447845B1 (en) | 2000-03-03 | 2002-09-10 | Dow Corning Corporation | Barrier coatings using polyacids |
| US6877745B1 (en) * | 2000-03-14 | 2005-04-12 | Walker Digital, Llc | Games of chance with player-specified elements |
| US6503305B1 (en) | 2000-05-18 | 2003-01-07 | Hammond Group, Inc. | Non-toxic corrosion inhibitor |
| DE10147784A1 (de) * | 2001-09-27 | 2003-04-17 | Univ Friedrich Alexander Er | Polymere Schutzschichten |
| US20050179010A1 (en) * | 2002-03-05 | 2005-08-18 | Chhiu-Tsu Lin | Surface base-coat formulation for metal alloys |
| JP2005528484A (ja) * | 2002-05-31 | 2005-09-22 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | 腐蝕抑制剤としてのアルキルアミノシロキサン |
| GB2400371B (en) * | 2003-04-04 | 2007-08-01 | Silberline Ltd | Metal pigment composition |
| CN1914356B (zh) | 2004-02-05 | 2010-05-05 | 日矿金属株式会社 | 金属的表面处理剂 |
| ITTO20050074A1 (it) * | 2005-02-10 | 2006-08-11 | Sorin Biomedica Cardio Srl | Protesi valvola cardiaca |
| US8541532B2 (en) | 2007-02-09 | 2013-09-24 | Nippon Shokubai Co., Ltd. | Silane compound, production method thereof, and resin composition containing silane compound |
| WO2008124706A2 (en) | 2007-04-06 | 2008-10-16 | Arizona Board Of Regents Acting For And On Behalf Of Arizona State University | Devices and methods for target molecule characterization |
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| US10259973B2 (en) * | 2009-03-13 | 2019-04-16 | Hi-Shear Corporation | Anti-corrosion and low friction metal pigmented coating |
| EP4657144A2 (en) | 2010-07-30 | 2025-12-03 | Alcon Inc. | Silicone hydrogel lenses with water-rich surfaces |
| TW201231512A (en) | 2010-10-15 | 2012-08-01 | Dow Corning | Silicon-containing materials with controllable microstructure |
| US9005700B2 (en) | 2011-10-12 | 2015-04-14 | Novartis Ag | Method for making UV-absorbing ophthalmic lenses |
| US9274430B2 (en) | 2012-10-10 | 2016-03-01 | Arizona Board Of Regents On Behalf Of Arizona State University | Systems and devices for molecule sensing and method of manufacturing thereof |
| US10338408B2 (en) | 2012-12-17 | 2019-07-02 | Novartis Ag | Method for making improved UV-absorbing ophthalmic lenses |
| US9981997B2 (en) | 2013-10-31 | 2018-05-29 | Arizona Board Of Regents On Behalf Of Arizona State University | Chemical reagents for attaching affinity molecules on surfaces |
| US9708087B2 (en) | 2013-12-17 | 2017-07-18 | Novartis Ag | Silicone hydrogel lens with a crosslinked hydrophilic coating |
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| CN117624954A (zh) * | 2015-10-21 | 2024-03-01 | 凯密特尔美国公司 | 胺官能化有机硅烷/脂肪酸组合体系作为施用于铝及其合金的污染/腐蚀抑制剂 |
| MY184638A (en) | 2015-12-15 | 2021-04-13 | Alcon Inc | Method for applying stable coating on silicone hydrogel contact lenses |
| EP3724698B1 (en) | 2017-12-13 | 2021-12-15 | Alcon Inc. | Method for producing mps-compatible water gradient contact lenses |
| TWI698442B (zh) * | 2018-12-10 | 2020-07-11 | 國立暨南國際大學 | 具遠紅外線放射性之二氧化矽複合粒子，其有機前驅物及複合粒子之應用 |
| US12365766B2 (en) * | 2021-09-02 | 2025-07-22 | Shin-Etsu Chemical Co., Ltd. | Organopolysiloxane composition |
| CN118835251B (zh) * | 2024-09-23 | 2024-12-03 | 成都恒固新材料科技有限公司 | 一种缓蚀剂组合物、其制备方法及应用 |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3773607A (en) * | 1971-06-17 | 1973-11-20 | Owens Corning Fiberglass Corp | Glass fiber reinforced elastomers |
| EP0195406A2 (en) * | 1985-03-18 | 1986-09-24 | Mitsubishi Petrochemical Co., Ltd. | Process for producing highly water-absorbing polymer |
| EP0344959A2 (en) * | 1988-06-03 | 1989-12-06 | Dow Corning Corporation | Ionomeric coupling agents based on amic acid-functional silanes |
| EP0648823A1 (en) * | 1993-10-15 | 1995-04-19 | Betz Europe, Inc. | Composition and process for coating metals |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4048206A (en) * | 1975-04-22 | 1977-09-13 | Mikhail Grigorievich Voronkov | Process for the production of 1-organylsilatranes and carbofunctional derivatives thereof |
| DE3338953A1 (de) * | 1983-10-27 | 1985-05-09 | Henkel KGaA, 4000 Düsseldorf | Verwendung von korrosionsinhibitoren in waessrigen systemen |
| GB8918086D0 (en) * | 1989-08-08 | 1989-09-20 | Ciba Geigy | Coating compositions |
| GB9101468D0 (en) * | 1991-01-23 | 1991-03-06 | Ciba Geigy | Coating compositions |
| GB9201642D0 (en) * | 1992-01-25 | 1992-03-11 | Ciba Geigy | Corrosion inhibitors |
| ES2095143T3 (es) * | 1993-04-07 | 1997-02-01 | Ciba Geigy Ag | Sales de metales alcalinoterreos, de metales de transicion y complejos de metales de transicion de acidos cetocarboxilicos como inhibidores de la corrosion. |
| US5489447A (en) * | 1993-06-25 | 1996-02-06 | Ciba-Geigy Corporation | Carrier-bound ketocarboxylic acids as corrosion inhibitors |
| TW327189B (en) * | 1994-01-18 | 1998-02-21 | Ciba Sc Holding Ag | Complexes of morpholine derivatives with keto-acids as corrosion inhibitors |
-
1996
- 1996-06-15 TW TW085107208A patent/TW428018B/zh active
- 1996-06-17 DK DK96922816T patent/DK0835289T3/da active
- 1996-06-17 AT AT96922816T patent/ATE180269T1/de not_active IP Right Cessation
- 1996-06-17 EA EA199800091A patent/EA000794B1/ru not_active IP Right Cessation
- 1996-06-17 US US08/981,434 patent/US5879436A/en not_active Expired - Fee Related
- 1996-06-17 CN CN96195143A patent/CN1117825C/zh not_active Expired - Fee Related
- 1996-06-17 CA CA002221776A patent/CA2221776A1/en not_active Abandoned
- 1996-06-17 DE DE69602530T patent/DE69602530T2/de not_active Expired - Fee Related
- 1996-06-17 WO PCT/EP1996/002600 patent/WO1997001606A1/en not_active Ceased
- 1996-06-17 KR KR1019970709974A patent/KR19990028652A/ko not_active Abandoned
- 1996-06-17 EP EP96922816A patent/EP0835289B1/en not_active Expired - Lifetime
- 1996-06-17 BR BR9609321A patent/BR9609321A/pt not_active IP Right Cessation
- 1996-06-17 ES ES96922816T patent/ES2133972T3/es not_active Expired - Lifetime
- 1996-06-17 JP JP9504133A patent/JPH11508927A/ja not_active Ceased
- 1996-06-17 AU AU63560/96A patent/AU699265B2/en not_active Ceased
- 1996-06-17 MX MX9710433A patent/MX9710433A/es not_active IP Right Cessation
- 1996-06-19 MY MYPI96002468A patent/MY129135A/en unknown
- 1996-06-26 SG SG1996010162A patent/SG43378A1/en unknown
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3773607A (en) * | 1971-06-17 | 1973-11-20 | Owens Corning Fiberglass Corp | Glass fiber reinforced elastomers |
| EP0195406A2 (en) * | 1985-03-18 | 1986-09-24 | Mitsubishi Petrochemical Co., Ltd. | Process for producing highly water-absorbing polymer |
| EP0344959A2 (en) * | 1988-06-03 | 1989-12-06 | Dow Corning Corporation | Ionomeric coupling agents based on amic acid-functional silanes |
| EP0648823A1 (en) * | 1993-10-15 | 1995-04-19 | Betz Europe, Inc. | Composition and process for coating metals |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2604241C2 (ru) * | 2013-02-19 | 2016-12-10 | Александр Валерьевич Бояринцев | Высокотехнологичное антикоррозийное теплоизоляционное покрытие с повышенными теплотехническими характеристиками |
| RU2625382C1 (ru) * | 2016-06-15 | 2017-07-13 | Общество с ограниченной ответственностью "Центр коррозионных испытаний" (ООО "Центр коррозионных испытаний") | Ингибитор коррозии и коррозионного растрескивания под напряжением |
| RU2676608C1 (ru) * | 2017-10-04 | 2019-01-09 | Общество С Ограниченной Ответственностью "Рустек" | Лакокрасочная композиция для получения тонких покрытий методом катодного электроосаждения |
| WO2019070146A1 (ru) * | 2017-10-04 | 2019-04-11 | Общество С Ограниченной Ответственностью "Рустек" | Лакокрасочная композиция для получения тонких покрытий методом катодного электроосаждения |
Also Published As
| Publication number | Publication date |
|---|---|
| MX9710433A (es) | 1998-03-31 |
| EP0835289A1 (en) | 1998-04-15 |
| US5879436A (en) | 1999-03-09 |
| EA199800091A1 (ru) | 1998-08-27 |
| EP0835289B1 (en) | 1999-05-19 |
| BR9609321A (pt) | 1999-07-06 |
| DE69602530D1 (de) | 1999-06-24 |
| JPH11508927A (ja) | 1999-08-03 |
| TW428018B (en) | 2001-04-01 |
| CN1117825C (zh) | 2003-08-13 |
| WO1997001606A1 (en) | 1997-01-16 |
| DK0835289T3 (da) | 1999-11-22 |
| CA2221776A1 (en) | 1997-01-16 |
| MY129135A (en) | 2007-03-30 |
| ES2133972T3 (es) | 1999-09-16 |
| SG43378A1 (en) | 1997-10-17 |
| AU699265B2 (en) | 1998-11-26 |
| DE69602530T2 (de) | 1999-10-28 |
| AU6356096A (en) | 1997-01-30 |
| ATE180269T1 (de) | 1999-06-15 |
| KR19990028652A (ko) | 1999-04-15 |
| CN1189849A (zh) | 1998-08-05 |
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Legal Events
| Date | Code | Title | Description |
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| MM4A | Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s) |
Designated state(s): AM AZ BY KZ KG MD TJ TM |
|
| MM4A | Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s) |
Designated state(s): RU |