CA2221776A1 - Aminosilane salts and silanamides of carboxylic acids as corrosion inhibitors - Google Patents
Aminosilane salts and silanamides of carboxylic acids as corrosion inhibitors Download PDFInfo
- Publication number
- CA2221776A1 CA2221776A1 CA002221776A CA2221776A CA2221776A1 CA 2221776 A1 CA2221776 A1 CA 2221776A1 CA 002221776 A CA002221776 A CA 002221776A CA 2221776 A CA2221776 A CA 2221776A CA 2221776 A1 CA2221776 A1 CA 2221776A1
- Authority
- CA
- Canada
- Prior art keywords
- c4alkyl
- hydrogen
- sulfur
- oxygen
- unsubstituted
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 230000007797 corrosion Effects 0.000 title claims abstract description 56
- 238000005260 corrosion Methods 0.000 title claims abstract description 56
- 239000003112 inhibitor Substances 0.000 title claims abstract description 40
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical class [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 title claims abstract description 17
- 150000001735 carboxylic acids Chemical class 0.000 title claims abstract description 10
- 150000003839 salts Chemical class 0.000 claims abstract description 79
- 239000008199 coating composition Substances 0.000 claims abstract description 56
- 229920002125 Sokalan® Polymers 0.000 claims abstract description 35
- 229920001577 copolymer Polymers 0.000 claims abstract description 32
- 239000004584 polyacrylic acid Substances 0.000 claims abstract description 32
- 150000001408 amides Chemical class 0.000 claims abstract description 27
- 239000001257 hydrogen Substances 0.000 claims description 175
- 229910052739 hydrogen Inorganic materials 0.000 claims description 175
- 229910052760 oxygen Inorganic materials 0.000 claims description 166
- 229910052717 sulfur Inorganic materials 0.000 claims description 165
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 164
- 239000011593 sulfur Substances 0.000 claims description 164
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 161
- 239000001301 oxygen Substances 0.000 claims description 161
- -1 naphthoxy Chemical group 0.000 claims description 142
- 150000002431 hydrogen Chemical group 0.000 claims description 113
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 103
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 92
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 61
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 47
- 229910052799 carbon Inorganic materials 0.000 claims description 40
- 150000001721 carbon Chemical group 0.000 claims description 39
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 38
- 125000001624 naphthyl group Chemical group 0.000 claims description 32
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 32
- 125000004432 carbon atom Chemical group C* 0.000 claims description 31
- 239000000203 mixture Substances 0.000 claims description 31
- 229910052736 halogen Inorganic materials 0.000 claims description 29
- 150000002367 halogens Chemical group 0.000 claims description 29
- 239000011248 coating agent Substances 0.000 claims description 27
- 238000000576 coating method Methods 0.000 claims description 27
- 239000003795 chemical substances by application Substances 0.000 claims description 25
- 238000002360 preparation method Methods 0.000 claims description 22
- 239000000460 chlorine Chemical group 0.000 claims description 21
- 229910052801 chlorine Inorganic materials 0.000 claims description 21
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 20
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- 239000011347 resin Substances 0.000 claims description 20
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 18
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 18
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 16
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 16
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 15
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- 239000002184 metal Substances 0.000 claims description 13
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims description 12
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- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims description 10
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- 239000003822 epoxy resin Substances 0.000 claims description 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
- 229920000647 polyepoxide Polymers 0.000 claims description 10
- 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 8
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- 239000004925 Acrylic resin Substances 0.000 claims description 7
- 125000004957 naphthylene group Chemical group 0.000 claims description 7
- 239000000758 substrate Substances 0.000 claims description 7
- 239000000945 filler Substances 0.000 claims description 6
- HVZWVEKIQMJYIK-UHFFFAOYSA-N nitryl chloride Chemical group [O-][N+](Cl)=O HVZWVEKIQMJYIK-UHFFFAOYSA-N 0.000 claims description 6
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 6
- 125000004956 cyclohexylene group Chemical group 0.000 claims description 5
- 238000011065 in-situ storage Methods 0.000 claims description 5
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 4
- 229920000180 alkyd Polymers 0.000 claims description 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 4
- 238000001723 curing Methods 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
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- 239000000049 pigment Substances 0.000 claims description 4
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- 239000002318 adhesion promoter Substances 0.000 claims description 3
- 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
- 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
- 229920006243 acrylic copolymer Polymers 0.000 claims description 2
- 239000003054 catalyst Substances 0.000 claims description 2
- 239000002270 dispersing agent Substances 0.000 claims description 2
- 239000000975 dye Substances 0.000 claims description 2
- 239000013008 thixotropic agent Substances 0.000 claims description 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 18
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims 9
- 125000006710 (C2-C12) alkenyl group Chemical group 0.000 claims 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 4
- JYNZIOFUHBJABQ-UHFFFAOYSA-N allyl-{6-[3-(4-bromo-phenyl)-benzofuran-6-yloxy]-hexyl-}-methyl-amin Chemical compound C=1OC2=CC(OCCCCCCN(C)CC=C)=CC=C2C=1C1=CC=C(Br)C=C1 JYNZIOFUHBJABQ-UHFFFAOYSA-N 0.000 claims 4
- 125000006832 (C1-C10) alkylene group Chemical group 0.000 claims 3
- 125000000081 (C5-C8) cycloalkenyl group Chemical group 0.000 claims 3
- 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 claims 3
- 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 claims 3
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical group FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 claims 3
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 claims 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 2
- 239000000463 material Substances 0.000 claims 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims 1
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims 1
- 239000003963 antioxidant agent Substances 0.000 claims 1
- 239000004611 light stabiliser Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 66
- 150000001875 compounds Chemical class 0.000 description 59
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 50
- 150000003254 radicals Chemical class 0.000 description 46
- 239000002253 acid Substances 0.000 description 32
- 238000012360 testing method Methods 0.000 description 29
- 239000005639 Lauric acid Substances 0.000 description 25
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 24
- 238000003756 stirring Methods 0.000 description 22
- 239000000243 solution Substances 0.000 description 21
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 18
- 239000007921 spray Substances 0.000 description 18
- 241001024304 Mino Species 0.000 description 17
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 15
- 229910052757 nitrogen Inorganic materials 0.000 description 14
- 238000009472 formulation Methods 0.000 description 13
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- 229910000831 Steel Inorganic materials 0.000 description 11
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 11
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- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 7
- CWAFVXWRGIEBPL-UHFFFAOYSA-N ethoxysilane Chemical compound CCO[SiH3] CWAFVXWRGIEBPL-UHFFFAOYSA-N 0.000 description 7
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- 235000019198 oils Nutrition 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 6
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- 101100274524 Mus musculus Clec18a gene Proteins 0.000 description 5
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- 125000004923 naphthylmethyl group Chemical group C1(=CC=CC2=CC=CC=C12)C* 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000010502 orange oil Substances 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 125000002971 oxazolyl group Chemical group 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004193 piperazinyl group Chemical group 0.000 description 1
- 125000003386 piperidinyl group Chemical group 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 125000001844 prenyl group Chemical group [H]C([*])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- UORVCLMRJXCDCP-UHFFFAOYSA-N propynoic acid Chemical compound OC(=O)C#C UORVCLMRJXCDCP-UHFFFAOYSA-N 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- WRHZVMBBRYBTKZ-UHFFFAOYSA-N pyrrole-2-carboxylic acid Chemical compound OC(=O)C1=CC=CN1 WRHZVMBBRYBTKZ-UHFFFAOYSA-N 0.000 description 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 238000003847 radiation curing Methods 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 150000003377 silicon compounds Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
- 125000003831 tetrazolyl group Chemical group 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 125000004306 triazinyl group Chemical group 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 229940045860 white wax Drugs 0.000 description 1
- 239000011787 zinc oxide 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
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Wood Science & Technology (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 | ||
| CH1911/95 | 1995-06-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2221776A1 true CA2221776A1 (en) | 1997-01-16 |
Family
ID=4221483
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002221776A Abandoned CA2221776A1 (en) | 1995-06-29 | 1996-06-17 | Aminosilane salts and silanamides of carboxylic acids as corrosion inhibitors |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US5879436A (2) |
| EP (1) | EP0835289B1 (2) |
| JP (1) | JPH11508927A (2) |
| KR (1) | KR19990028652A (2) |
| CN (1) | CN1117825C (2) |
| AT (1) | ATE180269T1 (2) |
| AU (1) | AU699265B2 (2) |
| BR (1) | BR9609321A (2) |
| CA (1) | CA2221776A1 (2) |
| DE (1) | DE69602530T2 (2) |
| DK (1) | DK0835289T3 (2) |
| EA (1) | EA000794B1 (2) |
| ES (1) | ES2133972T3 (2) |
| MX (1) | MX9710433A (2) |
| MY (1) | MY129135A (2) |
| SG (1) | SG43378A1 (2) |
| TW (1) | TW428018B (2) |
| WO (1) | WO1997001606A1 (2) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1999061384A1 (en) * | 1998-05-28 | 1999-12-02 | 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 |
| CA2484332A1 (en) * | 2002-05-31 | 2003-12-11 | Ciba Specialty Chemicals Holding Inc. | Alkylaminosiloxanes as corrosion inhibitors |
| 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 |
| US8968540B2 (en) | 2008-10-06 | 2015-03-03 | Arizona Board Of Regents, A Body Corporate Of The State Of Arizona Acting For And On Behalf Of Arizona State University | Trans-base tunnel reader for sequencing |
| US10259973B2 (en) * | 2009-03-13 | 2019-04-16 | Hi-Shear Corporation | Anti-corrosion and low friction metal pigmented coating |
| ES2980213T3 (es) | 2010-07-30 | 2024-09-30 | Alcon Inc | Lentes de hidrogel de silicona con superficies ricas en agua |
| TW201231512A (en) | 2010-10-15 | 2012-08-01 | Dow Corning | Silicon-containing materials with controllable microstructure |
| CA2851668C (en) | 2011-10-12 | 2016-08-16 | Novartis Ag | Method for making uv-absorbing ophthalmic lenses by coating |
| EP2906720A4 (en) | 2012-10-10 | 2016-06-01 | Univ Arizona | MOLECULAR BASED SYSTEMS AND DEVICES AND METHOD FOR PRODUCING THEM |
| HUE031702T2 (en) | 2012-12-17 | 2017-07-28 | Novartis Ag | A method for producing improved UV absorbing ophthalmic lenses |
| RU2604241C2 (ru) * | 2013-02-19 | 2016-12-10 | Александр Валерьевич Бояринцев | Высокотехнологичное антикоррозийное теплоизоляционное покрытие с повышенными теплотехническими характеристиками |
| 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 |
| MY180543A (en) | 2013-12-17 | 2020-12-01 | Novartis Ag | A silicone hydrogel lens with a crosslinked hydrophilic coating |
| WO2015131073A1 (en) | 2014-02-27 | 2015-09-03 | Arizona Board Of Regents Acting For And On Behalf Of Arizona State University | Triazole-based reader molecules and methods for synthesizing and use thereof |
| EP3186070B1 (en) | 2014-08-26 | 2019-09-25 | Novartis AG | Method for applying stable coating on silicone hydrogel contact lenses |
| CN104327221B (zh) * | 2014-10-21 | 2017-08-25 | 岳阳东方雨虹防水技术有限责任公司 | 一种抗锈蚀型水工专用聚羧酸减水剂及其制备方法 |
| US10258046B2 (en) | 2014-11-04 | 2019-04-16 | Allied Bioscience, Inc. | Antimicrobial coatings comprising quaternary silanes |
| KR102009127B1 (ko) * | 2014-11-04 | 2019-08-08 | 얼라이드 바이오사이언스, 인크. | 자가 오염제거 표면을 형성하기 위한 조성물 및 방법 |
| US10980236B2 (en) | 2014-11-04 | 2021-04-20 | Allied Bioscience, Inc. | Broad spectrum antimicrobial coatings comprising combinations of organosilanes |
| US10993441B2 (en) | 2014-11-04 | 2021-05-04 | Allied Bioscience, Inc. | Antimicrobial coatings comprising organosilane homopolymers |
| EP3256531A1 (en) | 2015-02-11 | 2017-12-20 | Allied Bioscience, Inc | Anti-microbial coating and method to form same |
| US20170114229A1 (en) * | 2015-10-21 | 2017-04-27 | Chemetall Us, Inc. | Amine-Functionalized Organosilane/Fatty Acid Combination Systems As Stain/Corrosion Inhibitors For The Application On Aluminum And Its Alloys |
| HUE051613T2 (hu) | 2015-12-15 | 2021-03-01 | Alcon Inc | Eljárás szilíciumhidrogél-kontaktlencsékre stabil kivonat felvitelére |
| 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 |
| WO2019070146A1 (ru) * | 2017-10-04 | 2019-04-11 | Общество С Ограниченной Ответственностью "Рустек" | Лакокрасочная композиция для получения тонких покрытий методом катодного электроосаждения |
| SG11202003456VA (en) | 2017-12-13 | 2020-07-29 | 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 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3773607A (en) * | 1971-06-17 | 1973-11-20 | Owens Corning Fiberglass Corp | Glass fiber reinforced elastomers |
| 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 |
| DE3682088D1 (de) * | 1985-03-18 | 1991-11-28 | Mitsubishi Petrochemical Co | Verfahren zur herstellung von wasserabsorbierenden polymeren. |
| US4871788A (en) * | 1988-06-03 | 1989-10-03 | Dow Corning Corporation | Inomeric coupling agents based on amic acid-functional silanes |
| 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 |
| EP0619290B1 (de) * | 1993-04-07 | 1996-10-09 | Ciba-Geigy Ag | Erdalkalimetallsalze, Uebergangsmetallsalze und Uebergangsmetallkomplexe von Ketocarbonsäuren als Korrosionsinhibitoren |
| US5489447A (en) * | 1993-06-25 | 1996-02-06 | Ciba-Geigy Corporation | Carrier-bound ketocarboxylic acids as corrosion inhibitors |
| US5412011A (en) * | 1993-10-15 | 1995-05-02 | Betz Laboratories, Inc. | Composition and process for coating metals |
| 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 KR KR1019970709974A patent/KR19990028652A/ko not_active Abandoned
- 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 JP JP9504133A patent/JPH11508927A/ja not_active Ceased
- 1996-06-17 MX MX9710433A patent/MX9710433A/es not_active IP Right Cessation
- 1996-06-17 DE DE69602530T patent/DE69602530T2/de not_active Expired - Fee Related
- 1996-06-17 BR BR9609321A patent/BR9609321A/pt not_active IP Right Cessation
- 1996-06-17 EP EP96922816A patent/EP0835289B1/en not_active Expired - Lifetime
- 1996-06-17 EA EA199800091A patent/EA000794B1/ru not_active IP Right Cessation
- 1996-06-17 CA CA002221776A patent/CA2221776A1/en not_active Abandoned
- 1996-06-17 DK DK96922816T patent/DK0835289T3/da active
- 1996-06-17 AU AU63560/96A patent/AU699265B2/en not_active Ceased
- 1996-06-17 ES ES96922816T patent/ES2133972T3/es not_active Expired - Lifetime
- 1996-06-17 WO PCT/EP1996/002600 patent/WO1997001606A1/en not_active Ceased
- 1996-06-17 AT AT96922816T patent/ATE180269T1/de not_active IP Right Cessation
- 1996-06-19 MY MYPI96002468A patent/MY129135A/en unknown
- 1996-06-26 SG SG1996010162A patent/SG43378A1/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| SG43378A1 (en) | 1997-10-17 |
| MX9710433A (es) | 1998-03-31 |
| AU699265B2 (en) | 1998-11-26 |
| KR19990028652A (ko) | 1999-04-15 |
| EA000794B1 (ru) | 2000-04-24 |
| EP0835289A1 (en) | 1998-04-15 |
| CN1117825C (zh) | 2003-08-13 |
| JPH11508927A (ja) | 1999-08-03 |
| CN1189849A (zh) | 1998-08-05 |
| AU6356096A (en) | 1997-01-30 |
| WO1997001606A1 (en) | 1997-01-16 |
| ES2133972T3 (es) | 1999-09-16 |
| MY129135A (en) | 2007-03-30 |
| EA199800091A1 (ru) | 1998-08-27 |
| ATE180269T1 (de) | 1999-06-15 |
| BR9609321A (pt) | 1999-07-06 |
| TW428018B (en) | 2001-04-01 |
| DE69602530D1 (de) | 1999-06-24 |
| US5879436A (en) | 1999-03-09 |
| DE69602530T2 (de) | 1999-10-28 |
| DK0835289T3 (da) | 1999-11-22 |
| EP0835289B1 (en) | 1999-05-19 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| FZDE | Discontinued |