EP3084035A1 - Method for the production of colored stainless steel surfaces - Google Patents
Method for the production of colored stainless steel surfacesInfo
- Publication number
- EP3084035A1 EP3084035A1 EP14780490.0A EP14780490A EP3084035A1 EP 3084035 A1 EP3084035 A1 EP 3084035A1 EP 14780490 A EP14780490 A EP 14780490A EP 3084035 A1 EP3084035 A1 EP 3084035A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- stainless steel
- colored
- sol
- coating
- gel
- 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.)
- Granted
Links
- 229910001220 stainless steel Inorganic materials 0.000 title claims abstract description 111
- 239000010935 stainless steel Substances 0.000 title claims abstract description 108
- 238000000034 method Methods 0.000 title claims abstract description 53
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 10
- 239000000049 pigment Substances 0.000 claims description 81
- 238000000576 coating method Methods 0.000 claims description 64
- 239000011248 coating agent Substances 0.000 claims description 50
- 239000002241 glass-ceramic Substances 0.000 claims description 25
- 239000007864 aqueous solution Substances 0.000 claims description 22
- 238000005524 ceramic coating Methods 0.000 claims description 19
- 239000008139 complexing agent Substances 0.000 claims description 19
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 16
- 150000003839 salts Chemical class 0.000 claims description 13
- 238000001029 thermal curing Methods 0.000 claims description 10
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 9
- 239000002904 solvent Substances 0.000 claims description 9
- 238000005507 spraying Methods 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 8
- 239000000377 silicon dioxide Substances 0.000 claims description 8
- 239000002932 luster Substances 0.000 claims description 7
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 229910000423 chromium oxide Inorganic materials 0.000 claims description 6
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims description 5
- 150000004756 silanes Chemical class 0.000 claims description 5
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 claims description 5
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims description 4
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 4
- 125000004999 nitroaryl group Chemical group 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 238000005096 rolling process Methods 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 229910052725 zinc Inorganic materials 0.000 claims description 2
- 229910052726 zirconium Inorganic materials 0.000 claims description 2
- 125000004103 aminoalkyl group Chemical group 0.000 claims 1
- 238000001228 spectrum Methods 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 64
- 238000005260 corrosion Methods 0.000 description 16
- 230000007797 corrosion Effects 0.000 description 16
- 239000000126 substance Substances 0.000 description 14
- 239000000463 material Substances 0.000 description 13
- 239000000203 mixture Substances 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 239000003086 colorant Substances 0.000 description 10
- 239000002245 particle Substances 0.000 description 10
- 239000000725 suspension Substances 0.000 description 10
- 238000002845 discoloration Methods 0.000 description 9
- 239000007800 oxidant agent Substances 0.000 description 9
- 239000003973 paint Substances 0.000 description 9
- 239000007858 starting material Substances 0.000 description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- 238000010790 dilution Methods 0.000 description 8
- 239000012895 dilution Substances 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 8
- 239000002184 metal Substances 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 6
- 229910045601 alloy Inorganic materials 0.000 description 6
- 239000000956 alloy Substances 0.000 description 6
- 239000002738 chelating agent Substances 0.000 description 6
- 229910052804 chromium Inorganic materials 0.000 description 6
- 239000011651 chromium Substances 0.000 description 6
- 239000001023 inorganic pigment Substances 0.000 description 6
- -1 iron ions Chemical class 0.000 description 6
- 238000001816 cooling Methods 0.000 description 5
- 238000004043 dyeing Methods 0.000 description 5
- 235000013980 iron oxide Nutrition 0.000 description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000009826 distribution Methods 0.000 description 4
- 230000002209 hydrophobic effect Effects 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- 239000004922 lacquer Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 238000005275 alloying Methods 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000011247 coating layer Substances 0.000 description 3
- 210000003298 dental enamel Anatomy 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 230000005484 gravity Effects 0.000 description 3
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 3
- 238000005204 segregation Methods 0.000 description 3
- 235000012239 silicon dioxide Nutrition 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- DBVJJBKOTRCVKF-UHFFFAOYSA-N Etidronic acid Chemical compound OP(=O)(O)C(O)(C)P(O)(O)=O DBVJJBKOTRCVKF-UHFFFAOYSA-N 0.000 description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 230000003666 anti-fingerprint Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- UOUJSJZBMCDAEU-UHFFFAOYSA-N chromium(3+);oxygen(2-) Chemical class [O-2].[O-2].[O-2].[Cr+3].[Cr+3] UOUJSJZBMCDAEU-UHFFFAOYSA-N 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 230000001143 conditioned effect Effects 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 238000001723 curing Methods 0.000 description 2
- YYLGKUPAFFKGRQ-UHFFFAOYSA-N dimethyldiethoxysilane Chemical compound CCO[Si](C)(C)OCC YYLGKUPAFFKGRQ-UHFFFAOYSA-N 0.000 description 2
- 238000004534 enameling Methods 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 150000002440 hydroxy compounds Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 2
- 238000005554 pickling Methods 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 238000004062 sedimentation Methods 0.000 description 2
- 239000011265 semifinished product Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 229910000077 silane Inorganic materials 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- CPUDPFPXCZDNGI-UHFFFAOYSA-N triethoxy(methyl)silane Chemical compound CCO[Si](C)(OCC)OCC CPUDPFPXCZDNGI-UHFFFAOYSA-N 0.000 description 2
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 1
- RMKZLFMHXZAGTM-UHFFFAOYSA-N [dimethoxy(propyl)silyl]oxymethyl prop-2-enoate Chemical compound CCC[Si](OC)(OC)OCOC(=O)C=C RMKZLFMHXZAGTM-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- RHZUVFJBSILHOK-UHFFFAOYSA-N anthracen-1-ylmethanolate Chemical compound C1=CC=C2C=C3C(C[O-])=CC=CC3=CC2=C1 RHZUVFJBSILHOK-UHFFFAOYSA-N 0.000 description 1
- 239000003830 anthracite Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- 239000001055 blue pigment Substances 0.000 description 1
- 230000000711 cancerogenic effect Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 231100000315 carcinogenic Toxicity 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- ITZXULOAYIAYNU-UHFFFAOYSA-N cerium(4+) Chemical class [Ce+4] ITZXULOAYIAYNU-UHFFFAOYSA-N 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000000536 complexating effect Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- WUUZKBJEUBFVMV-UHFFFAOYSA-N copper molybdenum Chemical compound [Cu].[Mo] WUUZKBJEUBFVMV-UHFFFAOYSA-N 0.000 description 1
- 231100001010 corrosive Toxicity 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 230000003670 easy-to-clean Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 229960004585 etidronic acid Drugs 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000000383 hazardous chemical Substances 0.000 description 1
- 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 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- ICIWUVCWSCSTAQ-UHFFFAOYSA-N iodic acid Chemical class OI(=O)=O ICIWUVCWSCSTAQ-UHFFFAOYSA-N 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 229910000734 martensite Inorganic materials 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- 239000002923 metal particle Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 231100000219 mutagenic Toxicity 0.000 description 1
- 230000003505 mutagenic effect Effects 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- IQZPDFORWZTSKT-UHFFFAOYSA-N nitrosulphonic acid Chemical class OS(=O)(=O)[N+]([O-])=O IQZPDFORWZTSKT-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000007781 pre-processing Methods 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 230000009993 protective function Effects 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000001054 red pigment Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 229910001256 stainless steel alloy Inorganic materials 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 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
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D1/00—Processes for applying liquids or other fluent materials
- B05D1/02—Processes for applying liquids or other fluent materials performed by spraying
-
- 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
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/02—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition
- C23C18/12—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition characterised by the deposition of inorganic material other than metallic material
- C23C18/1204—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition characterised by the deposition of inorganic material other than metallic material inorganic material, e.g. non-oxide and non-metallic such as sulfides, nitrides based compounds
- C23C18/1208—Oxides, e.g. ceramics
- C23C18/1212—Zeolites, glasses
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D1/00—Processes for applying liquids or other fluent materials
- B05D1/28—Processes for applying liquids or other fluent materials performed by transfer from the surfaces of elements carrying the liquid or other fluent material, e.g. brushes, pads, rollers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D3/00—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials
- B05D3/007—After-treatment
Definitions
- the present invention relates to a process for producing colored stainless steel surfaces having high durability and a wide range of uses, as well as articles or stainless steel having such surfaces.
- stainless steels are widely used in both technical and decorative applications.
- decorative applications such as architecture, interior design, furniture, paneling, kitchen equipment and automotive and railway construction is increasingly the desire loud colored stainless steel surfaces. These should not appear "painted or enamelled", but preserve their stainless steel character and have at least equivalent performance and corrosion resistance compared to non-colored surfaces.
- Stainless steel which is often referred to as stainless steel, is an iron alloy which, in addition to iron, may contain a number of other alloying elements such as chromium, nickel, molybdenum copper and others.
- An essential component of the stainless steel alloys is the element chromium, which is present in a minimum concentration of about 13 wt .-%, to ensure increased corrosion resistance of the steel.
- the chromium that is present in the alloy reacts with oxygen from the environment and forms a dense oxide layer on the surface, which protects the surface from corrosion (so-called passive layer).
- passive layer The quality and thus the corrosion resistance of passive layers depend on their structure and their content of chromium oxides and iron oxides. This is controlled classically by the concentration of alloying elements in the stainless steel.
- Coating layers consist of an organic matrix enriched with pigments as desired.
- Paints consist either of resins which are thinned with solvent and thus rendered paintable or sprayable. After application, the solvents evaporate, which solidifies the paint layers.
- Two-component paints consist of synthetic resins, which are mixed with a reactive substance (hardener) shortly before application, resulting in a polymerization process that solidifies the paints.
- Powder coatings consist of plastic powders which are electrostatically applied to the metal surfaces to be painted and then thermally baked.
- the powder layers are heated to temperatures in the range of 200 ° C to 250 ° C, whereby they melt and form a dense, smooth and closed layer on cooling.
- Coating layers are not very well suited for the production of colored stainless steel surfaces for several reasons:
- a chemical reaction of the metal with the chemicals in the bath over time forms a transparent chromium oxide layer of increasing thickness.
- the respective thickness of the layer determines the color effect. This is due to interference of the incident and reflected light on the surface similar to an oil film on water.
- the colors essentially correspond to the spectral colors and change with the viewing angle, so that large surfaces can be perceived uniformly only from a sufficiently large distance.
- Chemically colored stainless steel surfaces do not show a metallic sheen, but absorb up to 80% of the incident light and convert it into heat, so they look dark inside rooms and heat up significantly in the sunshine. The temperature resistance is limited to approx. 180 ° C. At higher temperatures, the color effect is lost.
- the rate of layer growth can not be actively controlled and is determined by the exact composition of the alloy and microstructure, the surface condition of the stainless steel and the temperature and composition of the dip bath. Smallest local deviations lead to differently rapid layer growth and thus to color deviations within the surfaces.
- Components consisting of two or more components are not uniformly colored by this method, as are deformed surfaces. Due to this, the method is only suitable for the treatment of semi-finished products such as sheets before further processing. Neither the exact colors that are created, nor the color depth or repeatability in the series are to control. In addition, the required chromium content in the alloy and the required homogeneity of the surface state of the dyeing ability set clear limits.
- Sol-gel coatings must be baked after application in order to be ceramized.
- the temperatures used for baking are in the range of 220 ° C to 400 ° C for a period of at least 30 minutes. Under these conditions, yellow or brownish discolorations of the surfaces occur in stainless steel.
- Transparent sol-gel layers on stainless steel can not be produced without discoloration of the surfaces according to the prior art without special pretreatment of the surfaces.
- Opaque colored layers are possible. They have a relatively high layer thickness, cover the discoloration of the stainless steel surfaces and look similar in appearance to enamel. A corresponding method is described in DE 197 15 940. Such surfaces do not meet the requirements of the market and are therefore not accepted.
- the present invention relates to a process for producing colored stainless steel surfaces having high durability and a wide range of uses, as well as articles having such stainless steel surfaces.
- the term "colored” here means that the color of the surface differs from the color of untreated stainless steel, for example, the surfaces in all achievable by inorganic pigments and their mixtures colors such as blue, brown, red, green, yellow, white, gray or black, wherein the metallic luster and structure is created by the stainless steel surface with its passive layer underlying the colored layer.
- the colored stainless steel surfaces produced according to the invention have on a chemically optimized passive layer a transparent, glass-ceramic coating which contains inorganic (usually non-transparent) color pigments and was produced by thermal curing of a sol-gel coating.
- the first step is to treat the natural stainless steel surface on the stainless steel surface with an aqueous solution containing a special combination of chelating and chelating agents to give the surfaces the necessary resistance to thermal discoloration.
- the next step for example by spraying, spraying or rolling a transparent silica-based sol-gel Applied coating and then thermally cured, wherein the layer thickness of the sol-gel coating during application is selected so that the final sol-gel coating after thermal curing has a layer thickness of preferably 1 to 3 ⁇ .
- the coating contains inorganic color pigments, which are deliberately introduced and distributed in arrangement and number in a manner that causes special color and gloss effects.
- the diameter of the color pigments is preferably below 1 pm and thus regularly below the thickness of the sol-gel layer.
- the usual diameters of the color pigments are in a range of 500 to 1500 nm.
- the number and distribution of the pigments per coated unit area is variable and is chosen so that the underlying stainless steel surfaces are not completely covered by the pigments and in substantial proportions by the transparent Coating remain visible. On the one hand this gives the surfaces colors with selectable color depth combined with the original metallic luster and the surface structure of the stainless steel surfaces.
- the surfaces according to the invention are colored, transparent reflective, inorganic, resistant to UV radiation and temperatures up to 400 ° C and corrosion. They are food-safe, water and dirt repellent and have anti-graffiti and anti-fingerprint properties.
- the invention relates to colored stainless steel surfaces, which overcome the disadvantages of the previous colored stainless steel surfaces and have significantly improved properties in terms of color design and usability, and a method for producing such colored stainless steel surfaces and objects with these colored stainless steel surfaces.
- articles of stainless steel can be completely or partially dyed.
- the entire surfaces or only certain areas of the surfaces can be colored. In the context of the present invention is thus a
- a surface to be colored is always to be understood in that the surface to be colored may be disposed on different surfaces of the stainless steel article or may also represent only certain locations of one or more surfaces thereof.
- the colored stainless steel surfaces according to the invention are first conditioned by pretreatment in such a way that they are insensitive to thermal decomposition. dyeings by temperatures up to 300 ° C. This pretreatment takes place in an aqueous solution which contains complexing agents, preferably a mixture of chelating agents and complexing agents, as described by way of example in the patent application
- WO 2008/107082 AI described aqueous solutions with complexing agents and the method for their use, which are also suitable for the inventive method.
- the conditioned surfaces i. the treated passive layer, an inorganic sol-gel coating, preferably based on silicon dioxide, applied with a layer thickness of preferably 0.5 to 5.0 .mu.m, preferably from 1 to 3 pm.
- the type of coating is chosen so that it is transparent and has a baking temperature below 300 ° C, preferably from 200 ° C to 250 ° C, so that the stainless steel surface does not discolour during baking.
- the selected sol-gel coating must have sufficient resistance to chemicals, temperature and corrosion. It must be permanently resistant to temperatures up to 400 ° C and in the salt spray test to withstand at least 200 hours load without damage.
- the sol-gel coating is added inorganic pigments, the colors are freely selectable.
- An essential property of the pigments is the size of the pigment grains. It should preferably be smaller than 1 ⁇ m in diameter.
- the size of the pigments can be adjusted by prior comminution, for example by a ball mill, and secured by filtration. This can ensure that later all the pigment particles are trapped in the sol-gel layer and sufficiently covered to protect it from corrosive attack. Furthermore, this ensures that the properties of the colored glass-ceramic coating are determined exclusively by the cured sol-gel itself and the pigments have no influence on the performance characteristics of the colored coatings.
- the defined size of the pigment granules allows a uniform distribution of the pigments on the surfaces to be coated in the coating process and improves the scattering of the incident light and the light reflected from the underlying stainless steel surface and increases the optical intensity of the colors. It has been found that the inorganic color pigments should have a diameter of 500 nm to 1,500 nm.
- the quantity and distribution of the pigment grains during application of the sol-gel layers are chosen such that they do not completely cover but completely cover the underlying stainless steel surfaces, and the latter are still partially uncovered and visible with their own gloss and structure. This preserves the metallic character of the coated surfaces.
- the amount of pigment grains per unit area color depth and color intensity in a wide range are freely selectable, the stainless steel surfaces with a slight color glimmer to intensely colored surfaces with
- the density and / or the distribution of the inorganic color pigments make possible a uniform arrangement of these pigments in the coating.
- the metal surface between the pigment particles still remains partially visible, so that the coated stainless steel surface still has a metallic luster.
- the process of the invention results in extensive and spontaneous separation of pigments and coating material.
- it may then come to a sedimentation of the pigments to the metal surface. This sedimentation takes place immediately after application of the coating material, whereby the coating solidifies at the same time or immediately thereafter by evaporation of the solvent contained in the coating material.
- a transparent, smooth cover layer of the sol-gel material is then obtained over the pigments.
- this sol-gel coating also exerts a protective function against the pigments, which are no longer directly vulnerable to environmental influences (including corrosion).
- the invention thus relates to a process for producing a transparent, colored stainless steel surface, comprising the steps:
- the method according to the invention can also be described as a method for producing a transparent, colored stainless steel surface or for producing articles which have a transparent, colored stainless steel surface, comprising the steps:
- complexing agent preferably a combination of complexing agents, and preferably at least one oxidizing agent to remove iron oxides and iron atoms from the passive layer on the stainless steel surface.
- Passive layer refers to the oxide layer that forms on a stainless steel surface. This oxide layer is colorless, transparent and consists mainly of iron oxides and chromium oxides.
- transparent colored Stainless steel surface means that a color impression is generated by inorganic pigments in the glass-ceramic coating, but - at locations where there are no pigments - light rays can fall through the glass-ceramic coating on the underlying stainless steel surface and are reflected by this again so that a metallic impression is created.
- the process according to the invention for the production of the colored stainless steel surfaces thus comprises the steps (i) to (iii), preferably it consists exclusively of these steps:
- stainless steel is provided.
- Stainless steel preferred according to the invention consists mainly of iron and contains at least 13% by weight of chromium.
- a limitation of the chromium content upwards is not given as well as with regard to other alloying elements such as nickel, molybdenum, manganese, silicon, copper, sulfur or phosphorus.
- Stainless steel according to the invention can have both an austenitic, ferritic or martensitic structure and also a ferritic-austenitic mixed structure (duplex structure).
- the metal compounds used regularly have a particle diameter of 1 to 100 nm or in the case of transparent layers from 1 to 20 nm.
- the suspensions used are therefore to be regarded as stable, so that one does not observe the desirable separation behavior according to the invention when applying the coating solution to a surface.
- stainless steels are materials with material numbers beginning with 1.4.
- the stainless steel surfaces to be dyed can have different gloss levels and structures by processing before dyeing.
- Such pre-processing methods are, for example, grinding, blasting, mechanical or electrolytic polishing, patterning or pickling.
- the stainless steel may be used as material / starting material, e.g. as steel sheet, or product, e.g. as part of a finished structure.
- the surface of the stainless steel to be colored should not be coated and, in particular, should be clean, free of grease and not corroded.
- existing coatings or corrosion products may be removed mechanically or chemically prior to application of the process of the present invention.
- the cleaning can be carried out, for example, in an alkaline decoction degreasing (for example with AK 161 from Schlötter), followed by rinsing the surface with water and drying.
- step (ii) the surfaces to be dyed are immersed in an aqueous solution containing a specific combination of organic chelating agents and complexing agents for a period of preferably 1-4 hours, more preferably 3-4 hours, as described in patent WO 2008 / 107082 AI and described herein. If appropriate, then a rinsing step with water.
- the resistance of the stainless steel surfaces against thermal discoloration is raised so much that the subsequent thermal curing of the sol-gel layers no discoloration of the bare stainless steel surfaces occurs.
- the type and amount of the complexing agents in the aqueous solution are preferably selected such that the ratio of chromium oxide to iron oxide in the passive layer is increased, preferably to a ratio of at least 4: 1.
- step (ii) should not be confused with a conventional pickling process in which metal is deliberately removed from the surface of a metallic workpiece (see DE 92 14 890 U1 and WO 88/00252 A1).
- the particular effect of the method according to the invention is attributable to the fact that a passive layer is not first produced, but an already existing passive layer in its composition and structure is changed in its composition and structure by the method steps according to the invention (step (ii)).
- the aqueous solution used in the chemical treatment comprises a complexing agent, preferably at least two complexing agents, and preferably an oxidizing agent.
- the complexing agents used are preferably multidentate complexing agents, so-called chelating agents. These polydentate complexing agents can remove iron from the passive layer by forming chelate complexes with the iron ions and helping to significantly increase the ratio of chromium oxide to iron oxide in the passive layer.
- the complexing agents used are preferably hydroxycarboxylic acids, phosphonic acids and organic nitrosulfonic acids.
- Another preferred ingredient of the aqueous solution in the chemical treatment is an oxidizing agent. This oxidizing agent should preferably be sufficient to ensure a normal potential of at least +300 mV in the solution. Suitable oxidizing agents include, for example, nitrates,
- Peroxo compounds, iodates and cerium (IV) compounds in the form of the respective acids or the corresponding water-soluble salts.
- peroxo compounds are peroxides, persulfates, perborates or else percarboxylates, such as
- a particularly suitable example of an aqueous solution which can be used in step (ii) of the treatment according to the present invention comprises the following composition:
- Alkylglykol 0.05-1.0 wt .-%, in particular 0.1-0.5 wt .-%, of at least one Alkylglykols the general structure H- (O-CHR-CH 2 ) n -OH, wherein R is hydrogen or a Is alkyl of 1-3 carbon atoms and n is 1-5, and
- the percentages given here refer to the respective pure substances or ions. If salts or compositions are used which contain other substances, such as counterions, water of crystallization, solvents, etc., correspondingly higher proportions by weight must be used.
- the at least one hydroxycarboxylic acid comprises citric acid, and / or the at least one phosphonic acid or hydroxyethane diphosphonic acid HEDP, and / or the at least one nitroaryl or nitroalkylsulfonic acid / 77-nitrobenzenesulfonic acid, and / or the at least one Al - kylglykol ethylene glycol and / or butyl glycol, and the oxidizing agent nitrate, peroxide, persulfate and / or cerium (IV) ions, in each case in the weight ratios indicated above.
- the aqueous solution preferably has a pH which is less than 7, preferably less than 4. This can be achieved by the aqueous solution containing at least one acid.
- a preferred method is that at least one of the complexing agents and / or at least one of the oxidizing agents is at least partially added in the form of an acid to the solution.
- Step (ii) of the treatment according to the present invention is carried out according to a preferred embodiment in an aqueous solution having a temperature of at most about 70 ° C. It is further preferred that the treatment takes place in aqueous solution at a temperature between room temperature and 60 ° C.
- the chemical treatment in aqueous solution is preferably carried out over a period of at least 60 minutes, for example, the chemical treatment can be carried out with an aqueous solution over a period of 1-4 hours.
- the workpiece is rinsed with water, preferably deionized water, to remove the passivating solution and dried before the workpiece is subjected to the treatment of step (iii).
- water preferably deionized water
- Step (iii) involves the formation of the glass-ceramic colored sol-gel coatings.
- Sol-gel coatings usually consist of two reaction components, which are mixed in a fixed ratio shortly before processing. This mixture is last added as a third component, a dilution, usually an alcohol. Dilution sets the concentration of the reaction mixture and the viscosity of the final batch.
- the sol-gel is first applied in the form of a liquid sol having colloidal particles suspended therein, which subsequently converts to a gel and, after thermal curing, finally forms a solid, hard topcoat. So if the "application of the sol-gel coating” or the “thermal hardening of the soi-gel coating” is mentioned, the expert knows in which state the sol-gel system is located.
- the sol-gel is preferably a silica sol based on silanes which are dissolved in solvents, wherein the silica sol preferably also contains one or more further sol-forming elements, preferably one or more elements from the group consisting of Al, Ti, Zr, Mg, Ca and Zn, these elements replacing the Si atoms in the colloidal structures.
- Preferred sol-gel coatings / sol-gel coatings are described in EP2145980. Reference is hereby made in particular to the sol-gel coatings described in EP2145980 and the process for their use.
- the starting compounds for forming the preferred sols and finally the sol-gel coating are preferably hydrolyzable silanes of the formula SiR 4 , where the 4 radicals R 2-4 comprise hydrolyzable radicals OR 'and 0-2 comprise nonhydrolyzable radicals R "
- the hydrolyzable radicals OR ' are hydroxy, alkoxy and / or cycloalkoxy radicals. Suitable examples thereof include, for example, hydroxy, methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, i-butoxy, t-butoxy, pentoxy, hexoxy, cyclopentyloxy, cyclohexyloxy, in particular Ethoxy, n-propoxy and isopropoxy are preferred.
- the hydrolyzable radicals OR ' may be identical or different from one another.
- the non-hydrolyzable radicals R " are alkyl and / or cycloalkyl radicals, suitable examples of which include, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, i-butyl, t-butyl, pentyl, hexyl, cyclopentyl, cyclohexyl radicals, particular preference being given to methyl, ethyl, n-propyl and isopropyl radicals
- the nonhydrolyzable radicals R " may also be identical or different from one another.
- the starting compounds of the preferred sols can consist of a single type of silane, but often they are mixtures of several silanes (and optionally additional sol-forming starting compounds of other elements).
- include. It is preferred that at least one of the components of the starting compounds is a silane of the formula Si (OR ') 4 -nR "n with n 0, ie Si (OR') 4-.
- a preferred sol-gel lacquer may be the starting materials TEOS
- MTES methyltriethoxysilane
- DMDES dimethyldiethoxysilane
- the starting compounds are partially hydrolyzed to the corresponding hydroxy compounds (such as orthosilicic acid, trihydroxyalkylsilane, etc.), which may be favored by the addition of a catalyst such as acid. Due to the high tendency for condensation of these hydroxy compounds, these can now condense with elimination of water to form smaller siloxane networks.
- OR 'and R “have the same meaning as above.
- the sol-gel coating preferably has a stoving temperature of below 300 ° C, preferably from 200 ° C to 250 ° C, on.
- the sol-gel coating is colorless before the addition of the inorganic color pigments.
- the color pigments are preferably applied as a suspension in the sol-gel.
- the amount of color pigments is adjusted so that the coated surfaces are only partially covered by pigments, so that preferably arranged below the glass ceramic layer stainless steel surface is visible with their passive layer through the glass-ceramic layer at the points where no inorganic color pigments are present.
- the viscosity of the sol-gel varnish can be adjusted by a person skilled in the art. It is known that the sol, with a correspondingly high dilution in its solvent, is sufficiently thin to be sprayed, sprayed, rolled or brushed
- Suitable solvents for the sol are water and especially alcohols such as methanol, ethanol, n-propanol or isopropanol, with ethanol and isopropanol being preferred because of their physical properties and the low toxicity of their vapors.
- the sol-gel used in step (iii) contains inorganic color pigments, e.g. SICOCER® Black 10901, SICOCER® Blue 2502, or SICOCER® Red 2355 from BASF.
- inorganic color pigments e.g. SICOCER® Black 10901, SICOCER® Blue 2502, or SICOCER® Red 2355 from BASF.
- one or more types of inorganic color pigments can be used. If different types of color pigments are used, they can be used in equal or different amounts.
- Amounts (g / kg) of pigments are used in the range of 10 g / kg to 300 g / kg, preferably 40 g / kg to 200 g / kg, based on the amount of sol gel.
- the amount of pigments (g / kg) is normalized by the specific gravity of the pigments so that always the same number of pigment grains per unit area (pigment density) is achieved.
- the inorganic color pigments preferably have a maximum diameter of 1 pm.
- the desired maximum diameter is ensured by sieving or filtration processes.
- the admixture of the pigments is carried out in the dilution, whereby the desired concentration of pigments in the final mixture is easily targeted.
- a suspension of the pigments is prepared by intensive stirring, the homogeneity of which is crucial for the uniformity of the coated surfaces. Since the density of the dilution and the pigments differ significantly, it is necessary throughout the entire production and coating process to mix sufficiently intensively in order to keep the suspension stable.
- the sol-gel coating prior to application, has a low viscosity similar to water and a significantly lower specific gravity than the suspended pigments. Therefore, the suspensions separate immediately after wear and the pigments attach themselves to the stainless steel surfaces. Due to the small size of the pigment grains thus a sufficient coverage of the pigment grains is ensured by the sol-gel layer.
- the properties of the coated stainless steel surfaces are thus determined solely by the properties of the sol-gel coating used and not by the properties of the processed pigments.
- the sol-gel coating in step (iii) is preferably applied by spraying or rolling, spraying or painting are also possible. Preferably, however, it is done by spraying, since this allows precise control of the amount applied per unit area.
- the surfaces can be dried until the solvent has evaporated.
- the dried surfaces are then thermally cured.
- the thermal curing in step (iii) is preferably carried out at a temperature of less than 300 ° C, preferably in a range of 200 ° C to 300 ° C.
- the curing takes place for a period of about 20 to 60, preferably 30 minutes at temperatures in the range of 160 ° C to 280 ° C, preferably 200 ° C to 250 ° C in air.
- the sol-gel (if the color pigments are disregarded) changes to a colorless, transparent, glassy layer.
- the thermal curing can be carried out regularly in the process according to the invention so that neither the color of the sol-gel coating nor the underlying stainless steel surface is changed. That is, the thermal stress of both the sol gel and the stainless steel surface does not cause discoloration that does not originate in the color pigments themselves.
- the glass-ceramic coating preferably has a thickness of 0.5-5.0 ⁇ m, preferably 1.0-5.0 ⁇ m, or 0.5-3.0 ⁇ m, and most preferably 1.0-3.0 ⁇ m.
- the glass-ceramic coating preferably has a uniform thickness
- the diameter of the inorganic color pigments / pigments is smaller than the diameter of the glass-ceramic coating which was produced from the sol-gel coating.
- Pigments whose diameter is equal to or greater than the layer thickness of the sol-gel layer are not or not sufficiently covered and protrude from the surface of the coating. They roughen the surface and are themselves exposed to the effects of corrosion and can cause pores in the coating resulting in localized corrosion of the underlying stainless steel surface
- the inventive method is largely independent of the alloy and the structure of stainless steel.
- the method according to the invention is applied to a stainless steel material consisting of composite parts, which are uniformly colored by the method according to the invention.
- the parts can be colored uniformly largely independent of their shape and shape.
- the surfaces of the invention have one or more of the performance characteristics recited herein in items 1-11.
- the colored surfaces still show the characteristics of the original stainless steel surfaces in terms of gloss and surface texture.
- the color choice is freely definable and repeatable at any time.
- the coloring is largely independent of the underlying material.
- Combined components and finished parts can be coated as well as sheets and other semi-finished products.
- the colored surfaces are resistant to corrosion and UV radiation.
- the colored surfaces are temperature resistant up to approx. 400 ° C.
- the colored surfaces are hydrophobic, easy to clean and exhibit
- the glass-ceramic coating according to the invention which was produced from the sol-gel coating, is transparent and not opaque. In particular, it has a metallic luster and reflects, depending on the density of the pigments, a substantial portion of the incident light. As a result, the surfaces appear much lighter in comparison to chemically colored surfaces.
- the coating is heat-resistant, the color effect at temperatures above 180 ° C and up to 300 ° C, especially at 200 ° C or 250 ° C, is not lost.
- the coating is also resistant to temperatures up to 400 ° C and can survive at least 200 hours load without damage in the salt spray test
- the invention also relates to stainless steel with a colored surface or objects made of stainless steel or with a surface made of stainless steel, wherein the stainless steel surface has a transparent, glass-ceramic coating containing inorganic color pigments.
- the colored surface can be prepared according to the method described herein. All embodiments described with respect to the method of the invention are also applicable to the colored surface products. In particular, the passive layer and glass-ceramic layer described with regard to the method is present on the stainless steel with a colored surface.
- the stainless steel surface is regularly only partially covered or optically hidden by the inorganic color pigments, so that a metallic surface arranged below the glass-ceramic layer is visible through the glass-ceramic layer at the points where no inorganic color pigments are present.
- the gloss and structure of the colored stainless steel surface also show the gloss and structure of the underlying stainless steel surfaces.
- the invention broadly relates to a stainless steel surface provided with a transparent colored glass-ceramic coating.
- the color of the coating results from the selected inorganic color pigments. These color pigments regularly have a diameter of 500 to 1500 nm. Im In the case of the present invention, it has been found that, especially with these pigment diameters, a metallic luster which very probably results from the metallic surface underlying the coating is retained. This would not be possible, for example, for coatings with pigments of smaller diameter, since the gloss is then masked.
- the invention also relates to colored stainless steel surfaces, produced or producible by the method according to the invention.
- a stainless steel sheet of 1.0 mm thickness of quality 1.4016 with bright annealed surface (method) and the dimensions 800 x 800 mm was cleaned in an alkaline Abkochentfettung for 15 minutes by dipping and then rinsed in water. Subsequently, the sheet was immersed in an aqueous solution with complexing and chelating agents (POLINOX-Protect from POLIGRAT GmbH) for 3 hours at 55 ° C.
- complexing and chelating agents POLINOX-Protect from POLIGRAT GmbH
- the sheet was lying by spraying coated with a layer thickness of 2 pm.
- a sol-gel coating based on silicon dioxide (POLIANT from POLIGRAT GmbH) was used, which was mixed with 100 g / kg of a blue pigment (SICOCER® Blue 2502). The pigment was ground into the dilution prior to admixing to a particle size below lpm.
- the surface was dried for 10 minutes and then baked in the oven at 220 ° C for 30 minutes.
- the surface After cooling, the surface showed a shiny metallic surface with intense blue, whereby a clear reflection of the environment in its natural colors was visible in the surface.
- the surface was smooth, hydrophobic and showed no fingerprints after touching.
- a stainless steel sheet of 1.5 mm thickness of quality 1.4301 with ground surface was pretreated as described in Example 1 and then lying coated with a sol-gel coating based on silica (POLIANT from POLIGRAT GmbH), wherein the dilution is a black pigment
- the surface was structured according to the microsection and felt smooth and metallic. It was hydrophobic and showed no fingerprints when touched.
- the workpiece was passivated, rinsed and dried for a period of 3 hours.
- the dry workpiece was coated on all sides by means of a spray gun with a sol-gel coating with a coating based on silicon dioxide (POLIANT from POLIGRAT GmbH). About the dilution, a pigment, a copper-red pigment (SICOCER® Rot 2355) in a concentration of 75 g / kg was added to the coating material.
- a pigment a copper-red pigment (SICOCER® Rot 2355) in a concentration of 75 g / kg was added to the coating material.
- the surfaces were baked at 220 ° C for 30 minutes. After cooling, the component showed on all sides a uniform shiny, copper-colored surface. The different materials including the welds showed uniform color and surface.
- the surfaces were smooth, glossy, hydrophobic and fingerprint resistant.
Abstract
Description
Claims
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EP14780490.0A EP3084035B1 (en) | 2013-12-18 | 2014-10-02 | Method for producing coloured stainless steel surfaces |
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EP13005900 | 2013-12-18 | ||
PCT/EP2014/071169 WO2015090660A1 (en) | 2013-12-18 | 2014-10-02 | Method for the production of colored stainless steel surfaces |
EP14780490.0A EP3084035B1 (en) | 2013-12-18 | 2014-10-02 | Method for producing coloured stainless steel surfaces |
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EP3084035B1 EP3084035B1 (en) | 2018-08-15 |
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EP (1) | EP3084035B1 (en) |
JP (1) | JP2017508066A (en) |
CN (1) | CN105849312A (en) |
CA (1) | CA2932979A1 (en) |
DK (1) | DK3084035T3 (en) |
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DE4338360A1 (en) * | 1993-11-10 | 1995-05-11 | Inst Neue Mat Gemein Gmbh | Process for the production of functional glass-like layers |
DE10064134A1 (en) * | 2000-12-19 | 2002-06-27 | Bsh Bosch Siemens Hausgeraete | Process for finishing metallic surfaces to avoid thermal tarnishing |
US20030138661A1 (en) * | 2003-02-19 | 2003-07-24 | Ferro Corporation | Sol-gel composition and method of making same |
DE102007010538A1 (en) * | 2007-03-05 | 2008-09-11 | Poligrat Gmbh | Process for the thermochemical passivation of stainless steel |
EP2182095A1 (en) * | 2008-10-29 | 2010-05-05 | Poligrat Gmbh | Method for treating stainless steel surfaces |
EP2206801A1 (en) * | 2008-12-24 | 2010-07-14 | Seb Sa | Composite cookware comprising a vitreous protective coating |
CN101914332A (en) * | 2010-09-09 | 2010-12-15 | 上海丰野表面处理剂有限公司 | Colorful fingerprint-resisting coating, preparation method and use method thereof |
KR20130109302A (en) * | 2012-03-27 | 2013-10-08 | 동부제철 주식회사 | Color-coated steel sheet and manufacturing method thereof |
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- 2014-10-02 RU RU2016127362A patent/RU2016127362A/en unknown
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DK3084035T3 (en) | 2018-10-15 |
WO2015090660A1 (en) | 2015-06-25 |
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CN105849312A (en) | 2016-08-10 |
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