DD239417A5 - Antikorrosive ueberzugsmittel - Google Patents

Antikorrosive ueberzugsmittel Download PDF

Info

Publication number: DD239417A5
Authority: DD; German Democratic Republic
Prior art keywords: item; acid; ylthio; coating agent; agent according
Prior art date: 1983-05-14

Application number

DD84262954A

Other languages

German (de)

English (en)

Inventor

Godwin Berner

William Hoyle

James Jack

Original Assignee

��`��@��k��

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

1984-05-11

Publication date

1986-09-24

1984-05-11 Application filed by ��`��@��k�� filed Critical ��`��@��k��

1986-09-24 Publication of DD239417A5 publication Critical patent/DD239417A5/de

Links

238000005260 corrosion Methods 0.000 claims abstract description 46
230000007797 corrosion Effects 0.000 claims abstract description 45
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 39
239000003112 inhibitor Substances 0.000 claims abstract description 36
239000008199 coating composition Substances 0.000 claims abstract description 20
150000001875 compounds Chemical class 0.000 claims abstract description 20
150000003839 salts Chemical class 0.000 claims abstract description 20
239000001257 hydrogen Substances 0.000 claims abstract description 16
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 16
150000002431 hydrogen Chemical class 0.000 claims abstract description 11
125000000217 alkyl group Chemical group 0.000 claims abstract description 10
229910052717 sulfur Inorganic materials 0.000 claims abstract description 10
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 9
239000011593 sulfur Chemical group 0.000 claims abstract description 9
125000001931 aliphatic group Chemical group 0.000 claims abstract description 7
125000001188 haloalkyl group Chemical group 0.000 claims abstract description 7
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 7
125000003884 phenylalkyl group Chemical group 0.000 claims abstract description 7
125000003545 alkoxy group Chemical group 0.000 claims abstract description 6
125000004414 alkyl thio group Chemical group 0.000 claims abstract description 5
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 5
125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 5
229910052736 halogen Inorganic materials 0.000 claims abstract description 5
150000002367 halogens Chemical class 0.000 claims abstract description 5
229910052760 oxygen Inorganic materials 0.000 claims abstract description 5
239000001301 oxygen Substances 0.000 claims abstract description 5
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 5
125000005037 alkyl phenyl group Chemical group 0.000 claims abstract description 4
125000004390 alkyl sulfonyl group Chemical group 0.000 claims abstract description 4
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims abstract description 4
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims abstract description 4
125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 3
125000001302 tertiary amino group Chemical group 0.000 claims abstract description 3
150000000000 tetracarboxylic acids Chemical class 0.000 claims abstract description 3
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-1 R is not -NH 2 Substances 0.000 claims description 101
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OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 4
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HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 4
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125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
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OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 3
125000004183 alkoxy alkyl group Chemical group 0.000 claims description 3
125000002947 alkylene group Chemical group 0.000 claims description 3
125000003277 amino group Chemical group 0.000 claims description 3
150000003863 ammonium salts Chemical class 0.000 claims description 3
238000004070 electrodeposition Methods 0.000 claims description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
125000002768 hydroxyalkyl group Chemical group 0.000 claims description 3
229910052742 iron Inorganic materials 0.000 claims description 3
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FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 2
150000001342 alkaline earth metals Chemical class 0.000 claims description 2
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239000011575 calcium Substances 0.000 claims description 2
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229910052802 copper Inorganic materials 0.000 claims description 2
239000010949 copper Substances 0.000 claims description 2
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239000011777 magnesium Substances 0.000 claims description 2
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239000003921 oil Substances 0.000 claims description 2
150000002894 organic compounds Chemical class 0.000 claims description 2
230000000737 periodic effect Effects 0.000 claims description 2
229920001568 phenolic resin Polymers 0.000 claims description 2
239000005011 phenolic resin Substances 0.000 claims description 2
229920002037 poly(vinyl butyral) polymer Polymers 0.000 claims description 2
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239000004645 polyester resin Substances 0.000 claims description 2
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229920002689 polyvinyl acetate Polymers 0.000 claims description 2
239000011118 polyvinyl acetate Substances 0.000 claims description 2
229920000915 polyvinyl chloride Polymers 0.000 claims description 2
239000004800 polyvinyl chloride Substances 0.000 claims description 2
239000011591 potassium Substances 0.000 claims description 2
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239000005060 rubber Substances 0.000 claims description 2
239000011734 sodium Substances 0.000 claims description 2
229910052708 sodium Inorganic materials 0.000 claims description 2
239000007787 solid Substances 0.000 claims description 2
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KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims 1
LVZWSLJZHVFIQJ-UHFFFAOYSA-N Cyclopropane Chemical compound C1CC1 LVZWSLJZHVFIQJ-UHFFFAOYSA-N 0.000 claims 1
239000003513 alkali Substances 0.000 claims 1
AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 claims 1
150000002484 inorganic compounds Chemical class 0.000 claims 1
229910010272 inorganic material Inorganic materials 0.000 claims 1
150000002902 organometallic compounds Chemical class 0.000 claims 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 claims 1
150000003512 tertiary amines Chemical class 0.000 claims 1
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims 1
230000002401 inhibitory effect Effects 0.000 abstract description 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
239000002253 acid Substances 0.000 description 53
125000004432 carbon atom Chemical group C* 0.000 description 13
229940125782 compound 2 Drugs 0.000 description 9
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 6
238000000576 coating method Methods 0.000 description 6
238000000034 method Methods 0.000 description 6
239000000243 solution Substances 0.000 description 6
ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 5
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 4
230000000694 effects Effects 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
239000002966 varnish Substances 0.000 description 4
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
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 3
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150000001412 amines Chemical class 0.000 description 3
IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 3
239000011230 binding agent Substances 0.000 description 3
VTYYLEPIZMXCLO-UHFFFAOYSA-L calcium carbonate Substances [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 3
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238000011156 evaluation Methods 0.000 description 3
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 3
229910052757 nitrogen Chemical class 0.000 description 3
239000007921 spray Substances 0.000 description 3
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239000011787 zinc oxide Substances 0.000 description 3
YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical class C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
RVDAYBAKAJCNNV-UHFFFAOYSA-N 2-(1,3-benzothiazol-2-ylsulfanylmethyl)butanedioate;hydron Chemical compound C1=CC=C2SC(SCC(CC(=O)O)C(O)=O)=NC2=C1 RVDAYBAKAJCNNV-UHFFFAOYSA-N 0.000 description 2
125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 2
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125000004861 4-isopropyl phenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
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125000003118 aryl group Chemical group 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
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229910052794 bromium Inorganic materials 0.000 description 2
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
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125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 2
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150000002170 ethers Chemical class 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
239000011737 fluorine Substances 0.000 description 2
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238000009472 formulation Methods 0.000 description 2
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
125000002887 hydroxy group Chemical class [H]O* 0.000 description 2
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
150000002611 lead compounds Chemical class 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 2
125000002347 octyl 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])[H] 0.000 description 2
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239000004848 polyfunctional curative Substances 0.000 description 2
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GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
239000002904 solvent Substances 0.000 description 2
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
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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
BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical class C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 description 1
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VLDPXPPHXDGHEW-UHFFFAOYSA-N 1-chloro-2-dichlorophosphoryloxybenzene Chemical compound ClC1=CC=CC=C1OP(Cl)(Cl)=O VLDPXPPHXDGHEW-UHFFFAOYSA-N 0.000 description 1
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OCBOWSUMTCOEGI-UHFFFAOYSA-N 2-(1,3-benzoxazol-2-ylsulfanylmethyl)butanedioate;dimethylazanium Chemical compound C[NH2+]C.C[NH2+]C.C1=CC=C2OC(SCC(CC(=O)[O-])C([O-])=O)=NC2=C1 OCBOWSUMTCOEGI-UHFFFAOYSA-N 0.000 description 1
PDRYYEGDSWKHHJ-UHFFFAOYSA-N 2-(1,3-benzoxazol-2-ylsulfanylmethyl)butanedioic acid Chemical compound C1=CC=C2OC(SCC(CC(=O)O)C(O)=O)=NC2=C1 PDRYYEGDSWKHHJ-UHFFFAOYSA-N 0.000 description 1
HPHITRLSNAKRGQ-UHFFFAOYSA-N 2-(1h-benzimidazol-2-ylsulfanyl)hexanedioic acid Chemical compound C1=CC=C2NC(SC(CCCC(=O)O)C(O)=O)=NC2=C1 HPHITRLSNAKRGQ-UHFFFAOYSA-N 0.000 description 1
PQSGCFJCMJTPFL-UHFFFAOYSA-N 2-(1h-benzimidazol-2-ylsulfanyl)pentanedioic acid Chemical compound C1=CC=C2NC(SC(CCC(=O)O)C(O)=O)=NC2=C1 PQSGCFJCMJTPFL-UHFFFAOYSA-N 0.000 description 1
JVMVNIBLHYHEIO-UHFFFAOYSA-N 2-(3-carboxy-1-oxo-1-sulfanylpropan-2-yl)-1,3-benzothiazole-5-carboxylic acid 3-(5-cyano-1,3-benzothiazol-2-yl)-4-oxo-4-sulfanylbutanoic acid 3-(6-methylsulfonyl-1,3-benzothiazol-2-yl)-4-oxo-4-sulfanylbutanoic acid 4-oxo-4-sulfanyl-3-[5-(trifluoromethyl)-1,3-benzothiazol-2-yl]butanoic acid Chemical compound C(#N)C=1C=CC2=C(N=C(S2)C(C(=S)O)CC(=O)O)C1.CS(=O)(=O)C1=CC2=C(N=C(S2)C(C(=S)O)CC(=O)O)C=C1.C(=O)(O)C=1C=CC2=C(N=C(S2)C(C(=S)O)CC(=O)O)C1.FC(C=1C=CC2=C(N=C(S2)C(C(=S)O)CC(=O)O)C1)(F)F JVMVNIBLHYHEIO-UHFFFAOYSA-N 0.000 description 1
FYCPEHYDYAUMGC-UHFFFAOYSA-N 2-(6-ethoxycarbonyl-1h-benzimidazol-2-yl)ethanethioic s-acid Chemical compound CCOC(=O)C1=CC=C2N=C(CC(S)=O)NC2=C1 FYCPEHYDYAUMGC-UHFFFAOYSA-N 0.000 description 1
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230000007935 neutral effect Effects 0.000 description 1
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical class N#N IJGRMHOSHXDMSA-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
229920003986 novolac Polymers 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
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
RZXMPPFPUUCRFN-UHFFFAOYSA-N p-toluidine Chemical compound CC1=CC=C(N)C=C1 RZXMPPFPUUCRFN-UHFFFAOYSA-N 0.000 description 1
238000002161 passivation Methods 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
230000010287 polarization Effects 0.000 description 1
229920001467 poly(styrenesulfonates) Polymers 0.000 description 1
229920001515 polyalkylene glycol Polymers 0.000 description 1
229920000768 polyamine Polymers 0.000 description 1
150000008442 polyphenolic compounds Chemical class 0.000 description 1
235000013824 polyphenols Nutrition 0.000 description 1
229920001021 polysulfide Polymers 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
239000000047 product Substances 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000011814 protection agent Substances 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
238000005096 rolling process Methods 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
238000005507 spraying Methods 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
230000002195 synergetic effect Effects 0.000 description 1
229920001864 tannin Chemical class 0.000 description 1
239000001648 tannin Chemical class 0.000 description 1
235000018553 tannin Nutrition 0.000 description 1
239000013008 thixotropic agent Substances 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
125000005208 trialkylammonium group Chemical group 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-O triethanolammonium Chemical compound OCC[NH+](CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-O 0.000 description 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 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
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
125000005023 xylyl group Chemical group 0.000 description 1
HPASKDOIHRJCCU-UHFFFAOYSA-L zinc 4-(1H-benzimidazol-2-yloxy)-4-sulfanylidenebutanoate Chemical compound N1=C(NC2=C1C=CC=C2)OC(CCC(=O)[O-])=S.[Zn+2].N2=C(NC1=C2C=CC=C1)OC(CCC(=O)[O-])=S HPASKDOIHRJCCU-UHFFFAOYSA-L 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)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Materials For Medical Uses (AREA)
External Artificial Organs (AREA)

DD84262954A 1983-05-14 1984-05-11 Antikorrosive ueberzugsmittel DD239417A5 (de)

Applications Claiming Priority (1)

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

Publications (1)

Publication Number	Publication Date
DD239417A5 true DD239417A5 (de)	1986-09-24

Family

ID=10542739

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD84262954A DD239417A5 (de)	1983-05-14	1984-05-11	Antikorrosive ueberzugsmittel

Country Status (13)

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

Families Citing this family (77)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB8313322D0 (en) *	1983-05-14	1983-06-22	Ciba Geigy Ag	Heterocyclic-(cyclo)aliphatic carboxylic acids
DE3341633A1 (de) *	1983-11-17	1985-05-30	Sanshin Kagaku Kogyo Co., Ltd., Yanai, Yamaguchi	Rosthemmende substanz
GB8412063D0 (en) *	1984-05-11	1984-06-20	Ciba Geigy Ag	Compositions containing heterocyclic corrosion inhibitors
GB8428677D0 (en) *	1984-11-13	1984-12-19	Ciba Geigy Ag	Corrosion-inhibiting aqueous coating compositions
US4873346A (en) *	1985-09-20	1989-10-10	The Upjohn Company	Substituted benzothiazoles, benzimidazoles, and benzoxazoles
EP0219336B1 (en) *	1985-10-14	1993-07-21	Hitachi Chemical Co., Ltd.	Liquid crystal orientation controlling film and liquid crystal device using the same
US4818777A (en) *	1986-08-27	1989-04-04	Ciba-Geigy Corporation	Phenolic corrosion inhibitors for coating materials
US4957704A (en) *	1988-08-09	1990-09-18	Pennzoil Products Company	Method of corrosion inhibition using hydrocarbyl polycarboxylates compositions
US5008153A (en) *	1988-12-08	1991-04-16	Ppg Industries, Inc.	Corrosion inhibitive pretreatment for "copper-free" mirrors
WO1990010095A1 (en) *	1989-02-24	1990-09-07	Itc Uniadvice Limited	Polymeric coating compositions for corrosion protection
EP0394196B1 (de) *	1989-04-20	1994-09-28	Ciba-Geigy Ag	Antikorrosive Anstrichstoffe
US5198482A (en) *	1989-12-14	1993-03-30	Ciba-Geigy Corporation	Corrosion-inhibiting coating compositions
US5051209A (en) *	1990-04-27	1991-09-24	E. I. Du Pont De Nemours And Company	Conductive epoxypolyamide coating composition
JPH0465184A (ja) *	1990-07-05	1992-03-02	Kansai Paint Co Ltd	電着前処理方法
US5302592A (en) *	1990-08-17	1994-04-12	Rohm And Haas Company	Use of substituted 3-thioacryloyl compounds as antimicrobial agents
JP3077193B2 (ja) *	1990-11-23	2000-08-14	株式会社デンソー	アルミニウム表面に耐食性化成皮膜を形成する方法
US5223025A (en) *	1991-09-03	1993-06-29	The Dexter Corporation	Coating composition for inhibiting corrosion of metal substrates
US5244738A (en) *	1991-09-03	1993-09-14	The Dexter Corporation	Metal article coated with a composition for inhibiting corrosion
GB9201642D0 (en) *	1992-01-25	1992-03-11	Ciba Geigy	Corrosion inhibitors
TW263534B (cs) *	1993-08-11	1995-11-21	Makkusu Kk
TW385328B (en) *	1995-06-14	2000-03-21	Ciba Sc Holding Ag	Corrosion inhibitors in powder coatings
US6059867A (en) *	1995-10-10	2000-05-09	Prc-Desoto International, Inc.	Non-chromate corrosion inhibitors for aluminum alloys
JP4194654B2 (ja) *	1995-10-10	2008-12-10	ピーアールシー−デソトインターナショナル，インコーポレイティド	アルミニウム合金用非クロム酸塩腐食防止剤
AU5561696A (en) *	1996-04-18	1997-11-07	International Business Machines Corporation	Organic-metallic composite coating for copper surface protection
US5780406A (en) *	1996-09-06	1998-07-14	Honda; Kenji	Non-corrosive cleaning composition for removing plasma etching residues
US6133342A (en)	1999-01-21	2000-10-17	Marconi Data Systems Inc.	Coating composition
EP1200201A1 (en)	1999-03-26	2002-05-02	David A. Lapoint	Articles coated with abrasion resistant coating
US6478861B1 (en)	1999-06-25	2002-11-12	Videojet Technologies Inc.	Laser markable coating
US6261348B1 (en) *	1999-06-25	2001-07-17	Marconi Data Systems Inc.	Laser markable coating
US6413923B2 (en) *	1999-11-15	2002-07-02	Arch Specialty Chemicals, Inc.	Non-corrosive cleaning composition for removing plasma etching residues
US7008980B2 (en) *	2001-01-18	2006-03-07	Awi Licensing Company	Waterborne coatings
BR0207618B1 (pt) *	2001-02-26	2011-09-06		tubo de aço sem costura com superfìcie tratada, método de fabricação do tubo de aço e lìquido para tratamento por conversão quìmica para um tubo de aço.
FR2822852B1 (fr) *	2001-03-27	2003-12-12	Usinor	Procede de traitement par carboxylatation de surfaces metalliques
US20040035498A1 (en) *	2002-06-04	2004-02-26	Lumimove, Inc. D/B/A/ Crosslink Polymer Research	Corrosion-responsive coating formulations for protection of metal surfaces
US20040191555A1 (en) *	2003-02-06	2004-09-30	Metal Coatings International Inc.	Coating systems having an anti-corrosion layer and a powder coating layer
US7271138B2 (en) *	2003-10-16	2007-09-18	The Procter & Gamble Company	Compositions for protecting glassware from surface corrosion in automatic dishwashing appliances
US7094740B2 (en) *	2003-10-16	2006-08-22	The Procter & Gamble Company	Zinc corrosion protection agents for treating glassware surfaces
US20050119154A1 (en) *	2003-10-16	2005-06-02	The Procter & Gamble Company	Methods for protecting glassware from surface corrosion in automatic dishwashing appliances
US7192639B2 (en) *	2004-01-14	2007-03-20	Hi-Shear Corporation	Chromate free corrosion resistant coating
US7101833B2 (en) *	2004-10-12	2006-09-05	The Procter & Gamble Company	Methods for treating glassware surfaces using zinc corrosion protection agents
EP1880416B1 (en) *	2005-05-10	2012-01-18	Dow Corning Corporation	Process for minimizing electromigration in an electronic device
US8231970B2 (en) *	2005-08-26	2012-07-31	Ppg Industries Ohio, Inc	Coating compositions exhibiting corrosion resistance properties and related coated substrates
US7745010B2 (en)	2005-08-26	2010-06-29	Prc Desoto International, Inc.	Coating compositions exhibiting corrosion resistance properties, related coated substrates, and methods
RU2456318C2 (ru) *	2008-07-21	2012-07-20	Ольга Федоровна Гвоздева	Водно-дисперсионная лакокрасочная композиция
CN102361857B (zh)	2008-09-26	2015-09-16	默沙东公司	可用作抗糖尿病剂的环状苯并咪唑衍生物
WO2010047982A1 (en)	2008-10-22	2010-04-29	Merck Sharp & Dohme Corp.	Novel cyclic benzimidazole derivatives useful anti-diabetic agents
WO2010051176A1 (en)	2008-10-29	2010-05-06	Merck Sharp & Dohme Corp.	Novel cyclic benzimidazole derivatives useful anti-diabetic agents
JP5557845B2 (ja)	2008-10-31	2014-07-23	メルク・シャープ・アンド・ドーム・コーポレーション	糖尿病用剤として有用な新規環状ベンゾイミダゾール誘導体
EP2528979A1 (en)	2010-01-29	2012-12-05	Hempel A/S	Epoxy-based primer compositions
US8895596B2 (en)	2010-02-25	2014-11-25	Merck Sharp & Dohme Corp	Cyclic benzimidazole derivatives useful as anti-diabetic agents
BR112013021236B1 (pt)	2011-02-25	2021-05-25	Merck Sharp & Dohme Corp	composto derivado de benzimidazol, e, composição
RU2495160C1 (ru) *	2012-05-30	2013-10-10	Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Российский химико-технологический университет им. Д.И. Менделеева" (РХТУ им. Д.И. Менделеева)	Водоразбавляемая полимерная композиция для покрытий
US9527875B2 (en)	2012-08-02	2016-12-27	Merck Sharp & Dohme Corp.	Antidiabetic tricyclic compounds
US9540364B2 (en)	2012-08-22	2017-01-10	Merck Sharp & Dohme Corp.	Benzimidazole tetrahydrofuran derivatives
US9527839B2 (en)	2012-08-22	2016-12-27	Merck Sharp & Dohme Corp.	Benzimidazole tetrahydropyran derivatives
WO2014031468A1 (en)	2012-08-22	2014-02-27	Merck Sharp & Dohme Corp.	Novel benzimidazole hexahydrofuro[3,2-b]furan derivatives
WO2014031517A1 (en)	2012-08-22	2014-02-27	Merck Sharp & Dohme Corp.	Novel azabenzimidazole tetrahydrofuran derivatives
WO2014031465A1 (en)	2012-08-22	2014-02-27	Merck Sharp & Dohme Corp.	Novel azabenzimidazole tetrahydropyran derivatives
RU2015109706A (ru)	2012-08-22	2016-10-10	Мерк Шарп И Доум Корп.	Новые производные азабензимидазол гексагидрофуро[3, 2-в]фурана
WO2014139388A1 (en)	2013-03-14	2014-09-18	Merck Sharp & Dohme Corp.	Novel indole derivatives useful as anti-diabetic agents
WO2015051496A1 (en)	2013-10-08	2015-04-16	Merck Sharp & Dohme Corp.	Antidiabetic tricyclic compounds
ES2747973T3 (es)	2013-11-15	2020-03-12	Merck Sharp & Dohme	Compuestos tricíclicos antidiabéticos
WO2015089809A1 (en)	2013-12-19	2015-06-25	Merck Sharp & Dohme Corp.	Antidiabetic substituted heteroaryl compounds
GB2527640B (en) *	2014-04-21	2022-09-21	Wilhelm Wieland Friedrich	Corrosion inhibitors, improved paint and corrosion protection coating
AT515756B1 (de) *	2014-04-21	2018-03-15	Wieland Kg	Korrosions-Inhibitoren, verbesserte Farbe und korrosionsschützende Beschichtung
US10669429B2 (en) *	2015-07-22	2020-06-02	Dow Global Technologies Llc	Ambient cure compositions for making coatings having humidity and corrosion resistance and methods of use
US10131813B2 (en) *	2015-07-22	2018-11-20	Dow Global Technologies Llc	Ambient cure compositions for making coatings having humidity and corrosion resistance and methods of use
CN106366897B (zh) *	2015-07-22	2021-06-04	陶氏环球技术有限责任公司	用于制备具有耐湿和耐腐蚀性涂层的环境固化组合物及使用方法
GB2543488B (en) *	2015-10-14	2022-02-02	Hexigone Inhibitors Ltd	Corrosion inhibitor
RU2735512C2 (ru) *	2015-11-13	2020-11-03	Эге Кымья Сан. Ве Тыдж. А. Ш.	Металлосодержащий уретанизированный полимер, растворимый в растворителе на основе низколетучего органического соединения
CN109312247B (zh) *	2016-04-07	2022-05-24	路博润公司	巯基吡咯衍生物作为润滑添加剂
US11149202B1 (en)	2016-12-13	2021-10-19	Ecolab Usa Inc.	Tetracarboxylic acid combinations for corrosion inhibition
ES2943158T3 (es) *	2020-04-03	2023-06-09	Atotech Deutschland Gmbh & Co Kg	Método para formar una capa de pasivación negra sobre una aleación de zinc-hierro y composición de pasivación negra
US12365803B2 (en) *	2020-06-19	2025-07-22	General Electric Company	Inspectable coatings and methods for using
JP7356175B2 (ja) *	2021-08-24	2023-10-04	サンノプコ株式会社	フラッシュラスト防止剤
US12319834B2 (en)	2021-12-17	2025-06-03	General Electric Company	Anti-corrosion material and application method
CN117466448A (zh) *	2023-12-18	2024-01-30	廊坊汇达精细化工有限公司	一种绿色复合缓蚀阻垢剂及其制备方法

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2154097A (en) *	1936-11-27	1939-04-11	Standard Oil Co	Lubricating oil
GB889380A (en) *	1959-12-04	1962-02-14	Basf Ag	Aqueous plastic dispersions containing corrosion inhibitors and hardening agents
CH458048A (de) *	1965-08-17	1968-06-15	Sandoz Ag	Verfahren zur Herstellung von optisch aufgehelltem Papier
JPS5919155B2 (ja) *	1975-09-01	1984-05-02	大日精化工業株式会社	有機質さび止顔料
US4329381A (en) *	1978-02-23	1982-05-11	Henkel Kommanditgesellschaft Auf Aktien (Henkel Kgaa)	Method for providing corrosion resistance to metal objects
US4235838A (en) *	1978-08-09	1980-11-25	Petrolite Corporation	Use of benzazoles as corrosion inhibitors
DE3046698A1 (de) *	1980-12-11	1982-07-15	Goslarer Farbenwerke Dr. Hans Heubach GmbH & Co KG, 3394 Langelsheim	Aluminiumzinkphosphathydrate bzw. basische aluminiumzinkphophathydrate, verfahren zu ihrer herstellung sowie ihre verwendung in anstrichmitteln
US4495336A (en) *	1982-06-07	1985-01-22	Petrolite Corporation	Mercapto-polycarboxylic acids
GB8313322D0 (en) *	1983-05-14	1983-06-22	Ciba Geigy Ag	Heterocyclic-(cyclo)aliphatic carboxylic acids

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

Also Published As

Publication number	Publication date
EP0128862B1 (de)	1989-03-01
ZA843575B (en)	1984-12-24
US4612049A (en)	1986-09-16
CS254975B2 (en)	1988-02-15
AU2794584A (en)	1984-11-15
CA1219745A (en)	1987-03-31
ATE41024T1 (de)	1989-03-15
JPS59215363A (ja)	1984-12-05
RU2032767C1 (ru)	1995-04-10
DK235484A (da)	1984-11-15
DK171712B1 (da)	1997-04-01
EP0128862A3 (en)	1986-06-11
DK235484D0 (da)	1984-05-11
JPH0543753B2 (cs)	1993-07-02
CS356784A2 (en)	1987-07-16
AU567738B2 (en)	1987-12-03
DE3476892D1 (en)	1989-04-06
EP0128862A2 (de)	1984-12-19
GB8313320D0 (en)	1983-06-22

Legal Events

Date	Code	Title	Description
1994-09-15	ENJ	Ceased due to non-payment of renewal fee
1994-09-29	ENJ	Ceased due to non-payment of renewal fee

Publication	Publication Date	Title
EP0128862B1 (de)	1989-03-01	Antikorrosive Überzugsmittel
EP0161222B1 (de)	1990-10-10	Heterocylische Mercaptocarbonsäureamide, -imide und -nitrile als Korrosionsinhibitoren
EP0161219B1 (de)	1991-06-12	Heterocyclische Mercaptocarbonsäure-ester und -anhydride als Korrosionsinhibitoren
DE69012486T2 (de)	1995-02-16	Überzugszusammensetzungen.
DE69309976T2 (de)	1997-11-27	Korrosionsinhibitoren
DE69223164T2 (de)	1998-03-19	Korrosionshemmende Überzugsmassen
EP0259255B1 (de)	1991-08-14	Phenolische Korrosionsinhibitoren für Anstrichstoffe
EP0619290B1 (de)	1996-10-09	Erdalkalimetallsalze, Uebergangsmetallsalze und Uebergangsmetallkomplexe von Ketocarbonsäuren als Korrosionsinhibitoren
DE68908438T2 (de)	1994-01-13	Zusammensetzungen und Verfahren zur Korrosionsinhibierung.
EP0394196A1 (de)	1990-10-24	Antikorrosive Anstrichstoffe
EP0183647B1 (de)	1989-02-15	Antikorrosive wässrige Anstrichstoffe
EP0669328B1 (de)	1998-09-30	Komplexe von Morpholinderivaten mit Ketocarbonsäuren als Korrosionsinhibitoren
US5198482A (en)	1993-03-30	Corrosion-inhibiting coating compositions
DE68905785T2 (de)	1993-08-12	Korrosionsinhibierende ueberzugsmassen.
DE3210540C1 (de)	1983-01-27	Kathodisch abscheidbare Elektrotauchlacke,Verfahren zu ihrer Herstellung und Verwendung
CN110791177A (zh)	2020-02-14	一种适用于漆中机械的防腐喷涂油漆
HK1003116B (en)	1998-10-09	Corrosion-inhibiting coating compositions
DE3503096C2 (de)	1987-03-19	Korrosionsschutzmittel
AT515756B1 (de)	2018-03-15	Korrosions-Inhibitoren, verbesserte Farbe und korrosionsschützende Beschichtung
DE3306064A1 (de)	1984-08-23	Korrosionsschutzueberzugsmittel