CS254975B2 - Anticorrosive priming coating means - Google Patents

Anticorrosive priming coating means Download PDF

Info

Publication number: CS254975B2
Authority: CS; Czechoslovakia
Prior art keywords: corrosion; benzthiazol; acid; salt; formula
Prior art date: 1983-05-14

Application number

CS843567A

Other languages

Czech (cs)

English (en)

Other versions

CS356784A2 (en

Inventor

Godwin Berner

William Hoyle

James Jack

Original Assignee

Ciba Geigy Ag

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1983-05-14

Filing date

1984-05-14

Publication date

1988-02-15

1984-05-14 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1987-07-16 Publication of CS356784A2 publication Critical patent/CS356784A2/cs

1988-02-15 Publication of CS254975B2 publication Critical patent/CS254975B2/cs

Links

238000000576 coating method Methods 0.000 title claims description 23
239000011248 coating agent Substances 0.000 title claims description 22
230000037452 priming Effects 0.000 title 1
238000005260 corrosion Methods 0.000 claims abstract description 48
230000007797 corrosion Effects 0.000 claims abstract description 47
239000003112 inhibitor Substances 0.000 claims abstract description 36
150000001875 compounds Chemical class 0.000 claims abstract description 19
150000003839 salts Chemical class 0.000 claims abstract description 17
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 15
125000001931 aliphatic group Chemical group 0.000 claims abstract description 5
125000000217 alkyl group Chemical group 0.000 claims abstract description 5
239000001257 hydrogen Substances 0.000 claims abstract description 4
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 4
150000000000 tetracarboxylic acids Chemical class 0.000 claims abstract description 3
150000003628 tricarboxylic acids Chemical class 0.000 claims abstract description 3
239000000049 pigment Substances 0.000 claims description 22
239000000758 substrate Substances 0.000 claims description 17
239000000203 mixture Substances 0.000 claims description 14
239000000945 filler Substances 0.000 claims description 9
229920000180 alkyd Polymers 0.000 claims description 8
125000004181 carboxyalkyl group Chemical group 0.000 claims description 8
239000003822 epoxy resin Substances 0.000 claims description 8
229920000647 polyepoxide Polymers 0.000 claims description 8
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 claims description 6
229920000178 Acrylic resin Polymers 0.000 claims description 5
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 5
239000004925 Acrylic resin Substances 0.000 claims description 4
239000007787 solid Substances 0.000 claims description 4
239000000126 substance Substances 0.000 claims description 2
239000008199 coating composition Substances 0.000 abstract description 5
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract description 2
230000002401 inhibitory effect Effects 0.000 abstract description 2
239000001301 oxygen Substances 0.000 abstract description 2
229910052760 oxygen Inorganic materials 0.000 abstract description 2
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
229910052717 sulfur Inorganic materials 0.000 abstract 2
239000011593 sulfur Chemical group 0.000 abstract 2
125000003545 alkoxy group Chemical group 0.000 abstract 1
125000005037 alkyl phenyl group Chemical group 0.000 abstract 1
125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
125000004414 alkyl thio group Chemical group 0.000 abstract 1
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
125000004093 cyano group Chemical group *C#N 0.000 abstract 1
125000000753 cycloalkyl group Chemical group 0.000 abstract 1
125000001188 haloalkyl group Chemical group 0.000 abstract 1
229910052736 halogen Inorganic materials 0.000 abstract 1
150000002367 halogens Chemical class 0.000 abstract 1
150000002431 hydrogen Chemical class 0.000 abstract 1
150000002763 monocarboxylic acids Chemical class 0.000 abstract 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
125000003884 phenylalkyl group Chemical group 0.000 abstract 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 abstract 1
125000001302 tertiary amino group Chemical group 0.000 abstract 1
-1 ferrous metals Chemical class 0.000 description 34
229910052751 metal Inorganic materials 0.000 description 21
239000002184 metal Substances 0.000 description 21
239000004922 lacquer Substances 0.000 description 11
229940125904 compound 1 Drugs 0.000 description 9
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 6
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 6
239000002253 acid Substances 0.000 description 6
239000002585 base Substances 0.000 description 6
229940125782 compound 2 Drugs 0.000 description 6
239000003973 paint Substances 0.000 description 6
239000000243 solution Substances 0.000 description 6
238000012360 testing method Methods 0.000 description 6
YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 5
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 5
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229920005989 resin Polymers 0.000 description 5
239000011347 resin Substances 0.000 description 5
239000008096 xylene Substances 0.000 description 5
ZPOQJHGXQZVXIO-UHFFFAOYSA-N 3-(1,3-benzothiazol-2-yl)-4-oxo-4-sulfanylbutanoic acid Chemical compound C1=CC=C2SC(C(C(O)=S)CC(=O)O)=NC2=C1 ZPOQJHGXQZVXIO-UHFFFAOYSA-N 0.000 description 4
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
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239000000654 additive Substances 0.000 description 4
125000004432 carbon atom Chemical group C* 0.000 description 4
ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 4
238000001035 drying Methods 0.000 description 4
150000002500 ions Chemical class 0.000 description 4
238000000034 method Methods 0.000 description 4
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229910052782 aluminium Inorganic materials 0.000 description 3
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
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239000011230 binding agent Substances 0.000 description 3
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238000001723 curing Methods 0.000 description 3
230000000694 effects Effects 0.000 description 3
238000009472 formulation Methods 0.000 description 3
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
229910052757 nitrogen Chemical class 0.000 description 3
239000000047 product Substances 0.000 description 3
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WXUAQHNMJWJLTG-UHFFFAOYSA-N 2-methylbutanedioic acid Chemical compound OC(=O)C(C)CC(O)=O WXUAQHNMJWJLTG-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
MZZSDCJQCLYLLL-UHFFFAOYSA-N Secalonsaeure A Natural products COC(=O)C12OC3C(CC1=C(O)CC(C)C2O)C(=CC=C3c4ccc(O)c5C(=O)C6=C(O)CC(C)C(O)C6(Oc45)C(=O)OC)O MZZSDCJQCLYLLL-UHFFFAOYSA-N 0.000 description 2
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
FMRLDPWIRHBCCC-UHFFFAOYSA-L Zinc carbonate Chemical compound [Zn+2].[O-]C([O-])=O FMRLDPWIRHBCCC-UHFFFAOYSA-L 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
229910052783 alkali metal Inorganic materials 0.000 description 2
229910052784 alkaline earth metal Inorganic materials 0.000 description 2
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
150000001735 carboxylic acids Chemical class 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
150000002170 ethers Chemical class 0.000 description 2
238000011156 evaluation Methods 0.000 description 2
229910052742 iron Inorganic materials 0.000 description 2
150000002611 lead compounds Chemical class 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 2
150000002989 phenols Chemical class 0.000 description 2
150000003077 polyols Chemical class 0.000 description 2
235000013824 polyphenols Nutrition 0.000 description 2
239000002904 solvent Substances 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
150000003751 zinc Chemical class 0.000 description 2
239000011667 zinc carbonate Substances 0.000 description 2
229910000010 zinc carbonate Inorganic materials 0.000 description 2
235000004416 zinc carbonate Nutrition 0.000 description 2
LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 2
229910000165 zinc phosphate Inorganic materials 0.000 description 2
OUPZKGBUJRBPGC-UHFFFAOYSA-N 1,3,5-tris(oxiran-2-ylmethyl)-1,3,5-triazinane-2,4,6-trione Chemical compound O=C1N(CC2OC2)C(=O)N(CC2OC2)C(=O)N1CC1CO1 OUPZKGBUJRBPGC-UHFFFAOYSA-N 0.000 description 1
UWWCBGSFTXGKLY-UHFFFAOYSA-N 1-(1,3-benzothiazol-2-ylsulfanyl)propane-1,2,3-tricarboxylic acid Chemical compound C1=CC=C2SC(SC(C(CC(=O)O)C(O)=O)C(O)=O)=NC2=C1 UWWCBGSFTXGKLY-UHFFFAOYSA-N 0.000 description 1
VLDPXPPHXDGHEW-UHFFFAOYSA-N 1-chloro-2-dichlorophosphoryloxybenzene Chemical compound ClC1=CC=CC=C1OP(Cl)(Cl)=O VLDPXPPHXDGHEW-UHFFFAOYSA-N 0.000 description 1
PFEIDOFHWNBJCW-UHFFFAOYSA-N 2-(1,3-benzothiazol-2-yl)-3-oxo-3-sulfanylpropanoic acid Chemical compound C1=CC=C2SC(C(C(O)=S)C(=O)O)=NC2=C1 PFEIDOFHWNBJCW-UHFFFAOYSA-N 0.000 description 1
WWIBNGQMJANCCI-UHFFFAOYSA-N 2-(1,3-benzothiazol-2-yl)ethanethioic s-acid Chemical compound C1=CC=C2SC(CC(=O)S)=NC2=C1 WWIBNGQMJANCCI-UHFFFAOYSA-N 0.000 description 1
DPEUAWJLUANAPE-UHFFFAOYSA-N 2-(1,3-benzothiazol-2-ylsulfanyl)-2,3-diethylbutanedioic acid Chemical compound C1=CC=C2SC(SC(CC)(C(C(O)=O)CC)C(O)=O)=NC2=C1 DPEUAWJLUANAPE-UHFFFAOYSA-N 0.000 description 1
QVIXXPMGBWKVKT-UHFFFAOYSA-N 2-(1,3-benzothiazol-2-ylsulfanyl)-3-ethylbutanedioic acid Chemical compound C1=CC=C2SC(SC(C(CC)C(O)=O)C(O)=O)=NC2=C1 QVIXXPMGBWKVKT-UHFFFAOYSA-N 0.000 description 1
LDMNNLWZGDLEDU-UHFFFAOYSA-N 2-(1,3-benzothiazol-2-ylsulfanyl)-3-methylbutanedioic acid Chemical compound C1=CC=C2SC(SC(C(C)C(O)=O)C(O)=O)=NC2=C1 LDMNNLWZGDLEDU-UHFFFAOYSA-N 0.000 description 1
MFEQJGPYUDTHGO-UHFFFAOYSA-N 2-(1,3-benzothiazol-2-ylsulfanyl)heptanedioic acid Chemical compound C1=CC=C2SC(SC(CCCCC(=O)O)C(O)=O)=NC2=C1 MFEQJGPYUDTHGO-UHFFFAOYSA-N 0.000 description 1
PVLUXKVHRRBCAL-UHFFFAOYSA-N 2-(1,3-benzothiazol-2-ylsulfanylmethyl)pentanedioic acid Chemical compound C1=CC=C2SC(SCC(CCC(=O)O)C(O)=O)=NC2=C1 PVLUXKVHRRBCAL-UHFFFAOYSA-N 0.000 description 1
SYKZLLFNVNXARA-UHFFFAOYSA-N 2-butan-2-ylsulfanyl-1,3-benzothiazole Chemical compound C1=CC=C2SC(SC(C)CC)=NC2=C1 SYKZLLFNVNXARA-UHFFFAOYSA-N 0.000 description 1
125000000143 2-carboxyethyl group Chemical group [H]OC(=O)C([H])([H])C([H])([H])* 0.000 description 1
QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
CAHWDGJDQYAFHM-UHFFFAOYSA-N 2-nitroisophthalic acid Chemical class OC(=O)C1=CC=CC(C(O)=O)=C1[N+]([O-])=O CAHWDGJDQYAFHM-UHFFFAOYSA-N 0.000 description 1
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YMLHUCYZPKLNMM-UHFFFAOYSA-N 3-(1,3-benzothiazol-2-ylsulfanyl)-2,2-dimethylbutanedioic acid Chemical compound C1=CC=C2SC(SC(C(C)(C)C(O)=O)C(O)=O)=NC2=C1 YMLHUCYZPKLNMM-UHFFFAOYSA-N 0.000 description 1
PQDBOAQFVABWDS-UHFFFAOYSA-N 3-(1,3-benzothiazol-2-ylsulfanyl)-3-methylbutanoic acid Chemical compound C1=CC=C2SC(SC(C)(CC(O)=O)C)=NC2=C1 PQDBOAQFVABWDS-UHFFFAOYSA-N 0.000 description 1
PPCADIOZLBZVLS-UHFFFAOYSA-N 3-(1,3-benzothiazol-2-ylsulfanyl)butanoic acid Chemical compound C1=CC=C2SC(SC(CC(O)=O)C)=NC2=C1 PPCADIOZLBZVLS-UHFFFAOYSA-N 0.000 description 1
VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
IWLATUURQBCQPI-UHFFFAOYSA-N 4-(1,3-benzothiazol-2-ylsulfanyl)butane-1,2,3-tricarboxylate;hydron Chemical compound C1=CC=C2SC(SCC(C(CC(=O)O)C(O)=O)C(O)=O)=NC2=C1 IWLATUURQBCQPI-UHFFFAOYSA-N 0.000 description 1
VLBFSFGWNXSNRM-UHFFFAOYSA-N 4-(1,3-benzothiazol-2-ylsulfanyl)butanoic acid Chemical compound C1=CC=C2SC(SCCCC(=O)O)=NC2=C1 VLBFSFGWNXSNRM-UHFFFAOYSA-N 0.000 description 1
HDPBBNNDDQOWPJ-UHFFFAOYSA-N 4-[1,2,2-tris(4-hydroxyphenyl)ethyl]phenol Chemical compound C1=CC(O)=CC=C1C(C=1C=CC(O)=CC=1)C(C=1C=CC(O)=CC=1)C1=CC=C(O)C=C1 HDPBBNNDDQOWPJ-UHFFFAOYSA-N 0.000 description 1
AXXCMMDHXJCEON-UHFFFAOYSA-N 5,5-dimethyl-1,3-bis(oxiran-2-ylmethyl)-6-propan-2-yl-1,3-diazinane-2,4-dione Chemical compound O=C1N(CC2OC2)C(=O)C(C)(C)C(C(C)C)N1CC1CO1 AXXCMMDHXJCEON-UHFFFAOYSA-N 0.000 description 1
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SXELPNSXOKOKTG-UHFFFAOYSA-N 5-(7-oxabicyclo[4.1.0]heptan-5-yloxy)-7-oxabicyclo[4.1.0]heptane Chemical compound C1CCC2OC2C1OC1C2OC2CCC1 SXELPNSXOKOKTG-UHFFFAOYSA-N 0.000 description 1
150000000565 5-membered heterocyclic compounds Chemical class 0.000 description 1
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UADAIMDTEUSTBS-UHFFFAOYSA-N 8-(1,3-benzothiazol-2-ylsulfanyl)octane-1,3,5,7-tetracarboxylic acid Chemical compound C1=CC=C2SC(SCC(CC(CC(CCC(=O)O)C(O)=O)C(O)=O)C(O)=O)=NC2=C1 UADAIMDTEUSTBS-UHFFFAOYSA-N 0.000 description 1
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239000005909 Kieselgur Substances 0.000 description 1
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ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
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150000008064 anhydrides Chemical class 0.000 description 1
PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
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239000007864 aqueous solution Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 1
230000004888 barrier function Effects 0.000 description 1
239000010428 baryte Substances 0.000 description 1
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239000011324 bead Substances 0.000 description 1
QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical class C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
NRIMHVFWRMABGJ-UHFFFAOYSA-N bicyclo[2.2.1]hepta-2,5-diene-2,3-dicarboxylic acid Chemical compound C1C2C(C(=O)O)=C(C(O)=O)C1C=C2 NRIMHVFWRMABGJ-UHFFFAOYSA-N 0.000 description 1
150000001642 boronic acid derivatives Chemical class 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
239000010974 bronze Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000011575 calcium Substances 0.000 description 1
159000000007 calcium salts Chemical class 0.000 description 1
MGYCIYIWDWWSIP-UHFFFAOYSA-L calcium;2-(1,3-benzothiazol-2-ylsulfanylmethyl)butanedioate Chemical compound [Ca+2].C1=CC=C2SC(SCC(CC(=O)[O-])C([O-])=O)=NC2=C1 MGYCIYIWDWWSIP-UHFFFAOYSA-L 0.000 description 1
230000000711 cancerogenic effect Effects 0.000 description 1
125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 1
239000000969 carrier Substances 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
239000003518 caustics Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
230000007665 chronic toxicity Effects 0.000 description 1
231100000160 chronic toxicity Toxicity 0.000 description 1
150000001868 cobalt Chemical class 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
238000007739 conversion coating Methods 0.000 description 1
239000000498 cooling water Substances 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 description 1
XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
229930003836 cresol Natural products 0.000 description 1
RRPVPGYVHCVLTI-UHFFFAOYSA-N ctk6d0458 Chemical compound C1C2OC2CC2OC21CC RRPVPGYVHCVLTI-UHFFFAOYSA-N 0.000 description 1
239000002173 cutting fluid Substances 0.000 description 1
IFDVQVHZEKPUSC-UHFFFAOYSA-N cyclohex-3-ene-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCC=CC1C(O)=O IFDVQVHZEKPUSC-UHFFFAOYSA-N 0.000 description 1
QSAWQNUELGIYBC-UHFFFAOYSA-N cyclohexane-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCCCC1C(O)=O QSAWQNUELGIYBC-UHFFFAOYSA-N 0.000 description 1
238000000151 deposition Methods 0.000 description 1
230000008021 deposition Effects 0.000 description 1
PLWAUKDWVYZWMT-UHFFFAOYSA-N diazanium;2-(1,3-benzothiazol-2-ylsulfanylmethyl)butanedioate Chemical compound [NH4+].[NH4+].C1=CC=C2SC(SCC(CC(=O)[O-])C([O-])=O)=NC2=C1 PLWAUKDWVYZWMT-UHFFFAOYSA-N 0.000 description 1
XUAQLTZKMUSZKS-UHFFFAOYSA-N diazanium;3-(1,3-benzothiazol-2-yl)-4-oxido-4-sulfanylidenebutanoate Chemical compound [NH4+].[NH4+].C1=CC=C2SC(C(C([O-])=S)CC(=O)[O-])=NC2=C1 XUAQLTZKMUSZKS-UHFFFAOYSA-N 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
GUJDNYLEGYTHGV-UHFFFAOYSA-L disodium;2-(1,3-benzothiazol-2-ylsulfanylmethyl)butanedioate Chemical compound [Na+].[Na+].C1=CC=C2SC(SCC(CC(=O)[O-])C([O-])=O)=NC2=C1 GUJDNYLEGYTHGV-UHFFFAOYSA-L 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
238000005553 drilling Methods 0.000 description 1
239000000975 dye Substances 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
238000004070 electrodeposition Methods 0.000 description 1
125000003700 epoxy group Chemical group 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000010304 firing Methods 0.000 description 1
239000011521 glass Substances 0.000 description 1
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
238000000227 grinding Methods 0.000 description 1
150000002440 hydroxy compounds Chemical class 0.000 description 1
125000004356 hydroxy functional group Chemical group O* 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
239000011630 iodine Substances 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
YOBAEOGBNPPUQV-UHFFFAOYSA-N iron;trihydrate Chemical compound O.O.O.[Fe].[Fe] YOBAEOGBNPPUQV-UHFFFAOYSA-N 0.000 description 1
239000001035 lead pigment Substances 0.000 description 1
150000007517 lewis acids Chemical class 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
239000001095 magnesium carbonate Substances 0.000 description 1
229910000021 magnesium carbonate Inorganic materials 0.000 description 1
239000000395 magnesium oxide Substances 0.000 description 1
CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
229910044991 metal oxide Inorganic materials 0.000 description 1
150000004706 metal oxides Chemical class 0.000 description 1
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
239000010705 motor oil Substances 0.000 description 1
JAYXSROKFZAHRQ-UHFFFAOYSA-N n,n-bis(oxiran-2-ylmethyl)aniline Chemical compound C1OC1CN(C=1C=CC=CC=1)CC1CO1 JAYXSROKFZAHRQ-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical class N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
229920003986 novolac Polymers 0.000 description 1
239000003921 oil Substances 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
125000002524 organometallic group Chemical group 0.000 description 1
TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
238000002161 passivation Methods 0.000 description 1
230000000737 periodic effect Effects 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
229920001568 phenolic resin Polymers 0.000 description 1
239000005011 phenolic resin Substances 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
150000003014 phosphoric acid esters Chemical class 0.000 description 1
150000003022 phthalic acids Chemical class 0.000 description 1
IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
230000010287 polarization Effects 0.000 description 1
229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
229920001515 polyalkylene glycol Polymers 0.000 description 1
229920001225 polyester resin Polymers 0.000 description 1
239000004645 polyester resin Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
150000008442 polyphenolic compounds Chemical class 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
229920005749 polyurethane resin Polymers 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
239000004800 polyvinyl chloride Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000001294 propane Substances 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
239000011814 protection agent Substances 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
230000005855 radiation Effects 0.000 description 1
239000001044 red dye Substances 0.000 description 1
GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 1
229960001755 resorcinol Drugs 0.000 description 1
239000005060 rubber Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
229920003048 styrene butadiene rubber Polymers 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
229920001864 tannin Polymers 0.000 description 1
239000001648 tannin Substances 0.000 description 1
235000018553 tannin Nutrition 0.000 description 1
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
UFDHBDMSHIXOKF-UHFFFAOYSA-N tetrahydrophthalic acid Natural products OC(=O)C1=C(C(O)=O)CCCC1 UFDHBDMSHIXOKF-UHFFFAOYSA-N 0.000 description 1
229920001187 thermosetting polymer Polymers 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1
239000013008 thixotropic agent Substances 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
125000005208 trialkylammonium group Chemical group 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
LOQGLYUREPUDGD-UHFFFAOYSA-N zinc;1,3-benzothiazole Chemical compound [Zn+2].C1=CC=C2SC=NC2=C1 LOQGLYUREPUDGD-UHFFFAOYSA-N 0.000 description 1
HHPNUNBIDCZUTN-UHFFFAOYSA-L zinc;2-(1,3-benzothiazol-2-ylsulfanylmethyl)butanedioate Chemical compound [Zn+2].C1=CC=C2SC(SCC(CC(=O)[O-])C([O-])=O)=NC2=C1 HHPNUNBIDCZUTN-UHFFFAOYSA-L 0.000 description 1
NDKWCCLKSWNDBG-UHFFFAOYSA-N zinc;dioxido(dioxo)chromium Chemical compound [Zn+2].[O-][Cr]([O-])(=O)=O NDKWCCLKSWNDBG-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- 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
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31678—Of metal
- Y10T428/31681—Next to polyester, polyamide or polyimide [e.g., alkyd, glue, or nylon, etc.]
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31678—Of metal
- Y10T428/31688—Next to aldehyde or ketone condensation product
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31678—Of metal
- Y10T428/31692—Next to addition polymer from unsaturated monomers

Landscapes

Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Organic Chemistry (AREA)
Paints Or Removers (AREA)
Preventing Corrosion Or Incrustation Of Metals (AREA)
Macromonomer-Based Addition Polymer (AREA)
External Artificial Organs (AREA)
Materials For Medical Uses (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CS843567A 1983-05-14 1984-05-14 Anticorrosive priming coating means CS254975B2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB838313320A GB8313320D0 (en)	1983-05-14	1983-05-14	Coating compositions

Publications (2)

Publication Number	Publication Date
CS356784A2 CS356784A2 (en)	1987-07-16
CS254975B2 true CS254975B2 (en)	1988-02-15

Family

ID=10542739

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS843567A CS254975B2 (en)	1983-05-14	1984-05-14	Anticorrosive priming coating means

Country Status (13)

Country	Link
US (1)	US4612049A (fr)
EP (1)	EP0128862B1 (fr)
JP (1)	JPS59215363A (fr)
AT (1)	ATE41024T1 (fr)
AU (1)	AU567738B2 (fr)
CA (1)	CA1219745A (fr)
CS (1)	CS254975B2 (fr)
DD (1)	DD239417A5 (fr)
DE (1)	DE3476892D1 (fr)
DK (1)	DK171712B1 (fr)
GB (1)	GB8313320D0 (fr)
RU (1)	RU2032767C1 (fr)
ZA (1)	ZA843575B (fr)

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1983
- 1983-05-14 GB GB838313320A patent/GB8313320D0/en active Pending
1984
- 1984-05-08 EP EP84810218A patent/EP0128862B1/fr not_active Expired
- 1984-05-08 AT AT84810218T patent/ATE41024T1/de not_active IP Right Cessation
- 1984-05-08 DE DE8484810218T patent/DE3476892D1/de not_active Expired
- 1984-05-11 DK DK235484A patent/DK171712B1/da not_active IP Right Cessation
- 1984-05-11 DD DD84262954A patent/DD239417A5/de not_active IP Right Cessation
- 1984-05-11 AU AU27945/84A patent/AU567738B2/en not_active Expired
- 1984-05-11 ZA ZA843575A patent/ZA843575B/xx unknown
- 1984-05-11 CA CA000454095A patent/CA1219745A/fr not_active Expired
- 1984-05-11 RU SU843737944A patent/RU2032767C1/ru active
- 1984-05-14 CS CS843567A patent/CS254975B2/cs unknown
- 1984-05-14 JP JP59094775A patent/JPS59215363A/ja active Granted
1985
- 1985-04-25 US US06/727,046 patent/US4612049A/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
EP0128862A3 (en)	1986-06-11
DE3476892D1 (en)	1989-04-06
AU2794584A (en)	1984-11-15
DK235484D0 (da)	1984-05-11
GB8313320D0 (en)	1983-06-22
AU567738B2 (en)	1987-12-03
DK171712B1 (da)	1997-04-01
CA1219745A (fr)	1987-03-31
ZA843575B (en)	1984-12-24
JPS59215363A (ja)	1984-12-05
EP0128862B1 (fr)	1989-03-01
DD239417A5 (de)	1986-09-24
JPH0543753B2 (fr)	1993-07-02
CS356784A2 (en)	1987-07-16
EP0128862A2 (fr)	1984-12-19
DK235484A (da)	1984-11-15
RU2032767C1 (ru)	1995-04-10
US4612049A (en)	1986-09-16
ATE41024T1 (de)	1989-03-15

Publication	Publication Date	Title
US4612049A (en)	1986-09-16	Corrosion-inhibiting coating compositions
JP2565862B2 (ja)	1996-12-18	複素環式腐食防止剤
JP2547316B2 (ja)	1996-10-23	複素環式腐蝕防止剤
RU2019550C1 (ru)	1994-09-15	Способ получения ингибирующего коррозию лакокрасочного материала
CZ389990A3 (cs)	1999-03-17	Nátěrové hmoty a jejich použití
JPH0680906A (ja)	1994-03-22	腐食阻止剤
JP7831839B2 (ja)	2026-03-17	水性防食塗料組成物
EP0330613B1 (fr)	1993-08-18	Compositions et procédé pour inhiber la corrosion
US5226956A (en)	1993-07-13	Surface coating compositions
Müller et al.	1996	Heterocycles as corrosion inhibitors for zinc pigments in aqueous alkaline media
CA1316685C (fr)	1993-04-27	Composes aqueux anti-corrosion
EP0375614B1 (fr)	1993-03-31	Compositions de revêtement inhibitrices de la corrosion
US5198482A (en)	1993-03-30	Corrosion-inhibiting coating compositions
US5519074A (en)	1996-05-21	Complexes of morpholine derivatives with keto-acids as corrosion inhibitors
JPS63314283A (ja)	1988-12-22	表面被覆組成物
US10669434B2 (en)	2020-06-02	Corrosion resistant coatings for metal surfaces
KR910003848B1 (ko)	1991-06-12	방청 도료
HK1003116B (en)	1998-10-09	Corrosion-inhibiting coating compositions
US20160075886A1 (en)	2016-03-17	Corrosion resistant coatings for metal surfaces
EP0385941A2 (fr)	1990-09-05	Compositions résistant à la corrosion
US20200255673A1 (en)	2020-08-13	Corrosion inhibitor for anti-corrosion coatings
JPS6216229B2 (fr)	1987-04-11
JPH02185574A (ja)	1990-07-19	塗料組成物