EP1366331A1 - Method for producing a coating on a quasi-continuously fed material strip - Google Patents
Method for producing a coating on a quasi-continuously fed material stripInfo
- Publication number
- EP1366331A1 EP1366331A1 EP02702389A EP02702389A EP1366331A1 EP 1366331 A1 EP1366331 A1 EP 1366331A1 EP 02702389 A EP02702389 A EP 02702389A EP 02702389 A EP02702389 A EP 02702389A EP 1366331 A1 EP1366331 A1 EP 1366331A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- coating agent
- coating
- material strip
- electromagnetic radiation
- radiation
- 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
- 239000011248 coating agent Substances 0.000 title claims abstract description 155
- 239000000463 material Substances 0.000 title claims abstract description 129
- 238000000576 coating method Methods 0.000 title claims abstract description 74
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 17
- 238000000034 method Methods 0.000 claims abstract description 70
- 230000005670 electromagnetic radiation Effects 0.000 claims abstract description 43
- 230000005855 radiation Effects 0.000 claims description 52
- 238000001035 drying Methods 0.000 claims description 40
- 238000004132 cross linking Methods 0.000 claims description 39
- 229910052751 metal Inorganic materials 0.000 claims description 36
- 239000002184 metal Substances 0.000 claims description 36
- 239000003973 paint Substances 0.000 claims description 24
- 239000000843 powder Substances 0.000 claims description 23
- 239000004922 lacquer Substances 0.000 claims description 17
- 229910000831 Steel Inorganic materials 0.000 claims description 12
- 239000010959 steel Substances 0.000 claims description 12
- 238000005260 corrosion Methods 0.000 claims description 10
- 230000007797 corrosion Effects 0.000 claims description 8
- 239000000758 substrate Substances 0.000 claims description 8
- 229910052736 halogen Inorganic materials 0.000 claims description 7
- 150000002367 halogens Chemical class 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- 230000005540 biological transmission Effects 0.000 claims description 6
- 238000006243 chemical reaction Methods 0.000 claims description 6
- 238000010521 absorption reaction Methods 0.000 claims description 5
- 239000002131 composite material Substances 0.000 claims description 5
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- 229920001169 thermoplastic Polymers 0.000 claims description 5
- 239000004416 thermosoftening plastic Substances 0.000 claims description 5
- 230000015572 biosynthetic process Effects 0.000 claims description 4
- 239000000470 constituent Substances 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 4
- 229920002120 photoresistant polymer Polymers 0.000 claims description 4
- 238000010408 sweeping Methods 0.000 claims description 4
- 239000011521 glass Substances 0.000 claims description 3
- 239000002985 plastic film Substances 0.000 claims description 2
- 229920006255 plastic film Polymers 0.000 claims description 2
- 239000000109 continuous material Substances 0.000 claims 1
- 239000010410 layer Substances 0.000 description 20
- 230000008569 process Effects 0.000 description 20
- 239000002904 solvent Substances 0.000 description 18
- 239000008199 coating composition Substances 0.000 description 13
- 239000007789 gas Substances 0.000 description 13
- 239000000049 pigment Substances 0.000 description 13
- 238000010438 heat treatment Methods 0.000 description 12
- 239000011230 binding agent Substances 0.000 description 9
- 239000007787 solid Substances 0.000 description 8
- 229920000642 polymer Polymers 0.000 description 7
- 239000010409 thin film Substances 0.000 description 7
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 6
- 239000000654 additive Substances 0.000 description 6
- 238000007796 conventional method Methods 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- -1 polyethylene Polymers 0.000 description 6
- 229910052782 aluminium Inorganic materials 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000003999 initiator Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 230000001965 increasing effect Effects 0.000 description 4
- 238000005245 sintering Methods 0.000 description 4
- 230000003595 spectral effect Effects 0.000 description 4
- 238000012546 transfer Methods 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 229910045601 alloy Inorganic materials 0.000 description 3
- 239000000956 alloy Substances 0.000 description 3
- 238000005452 bending Methods 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 238000004049 embossing Methods 0.000 description 3
- 239000010408 film Substances 0.000 description 3
- 239000012528 membrane Substances 0.000 description 3
- 239000010445 mica Substances 0.000 description 3
- 229910052618 mica group Inorganic materials 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
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- 239000004645 polyester resin Substances 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 238000002310 reflectometry Methods 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 239000004408 titanium dioxide Substances 0.000 description 3
- MFEVGQHCNVXMER-UHFFFAOYSA-L 1,3,2$l^{2}-dioxaplumbetan-4-one Chemical compound [Pb+2].[O-]C([O-])=O MFEVGQHCNVXMER-UHFFFAOYSA-L 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229910000003 Lead carbonate Inorganic materials 0.000 description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- AUNAPVYQLLNFOI-UHFFFAOYSA-L [Pb++].[Pb++].[Pb++].[O-]S([O-])(=O)=O.[O-][Cr]([O-])(=O)=O.[O-][Mo]([O-])(=O)=O Chemical compound [Pb++].[Pb++].[Pb++].[O-]S([O-])(=O)=O.[O-][Cr]([O-])(=O)=O.[O-][Mo]([O-])(=O)=O AUNAPVYQLLNFOI-UHFFFAOYSA-L 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 239000002318 adhesion promoter Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 239000003990 capacitor Substances 0.000 description 2
- 238000010538 cationic polymerization reaction Methods 0.000 description 2
- IAQWMWUKBQPOIY-UHFFFAOYSA-N chromium(4+);oxygen(2-) Chemical compound [O-2].[O-2].[Cr+4] IAQWMWUKBQPOIY-UHFFFAOYSA-N 0.000 description 2
- AYTAKQFHWFYBMA-UHFFFAOYSA-N chromium(IV) oxide Inorganic materials O=[Cr]=O AYTAKQFHWFYBMA-UHFFFAOYSA-N 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 238000001723 curing Methods 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 238000007306 functionalization reaction Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- 230000001939 inductive effect Effects 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 239000004973 liquid crystal related substance Substances 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 229910001416 lithium ion Inorganic materials 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 238000004886 process control Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 238000010526 radical polymerization reaction Methods 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 238000007788 roughening Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- 239000002966 varnish Substances 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 229910001111 Fine metal Inorganic materials 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 241000238370 Sepia Species 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 229910001297 Zn alloy Inorganic materials 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 239000002313 adhesive film Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- AOADSHDCARXSGL-ZMIIQOOPSA-M alkali blue 4B Chemical compound CC1=CC(/C(\C(C=C2)=CC=C2NC2=CC=CC=C2S([O-])(=O)=O)=C(\C=C2)/C=C/C\2=N\C2=CC=CC=C2)=CC=C1N.[Na+] AOADSHDCARXSGL-ZMIIQOOPSA-M 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- UHHXUPJJDHEMGX-UHFFFAOYSA-K azanium;manganese(3+);phosphonato phosphate Chemical compound [NH4+].[Mn+3].[O-]P([O-])(=O)OP([O-])([O-])=O UHHXUPJJDHEMGX-UHFFFAOYSA-K 0.000 description 1
- IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- 230000008033 biological extinction Effects 0.000 description 1
- GLQBXSIPUULYOG-UHFFFAOYSA-M bismuth oxychloride Chemical compound Cl[Bi]=O GLQBXSIPUULYOG-UHFFFAOYSA-M 0.000 description 1
- 239000001055 blue pigment Substances 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- CJOBVZJTOIVNNF-UHFFFAOYSA-N cadmium sulfide Chemical compound [Cd]=S CJOBVZJTOIVNNF-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 238000009750 centrifugal casting Methods 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 229930002875 chlorophyll Natural products 0.000 description 1
- 235000019804 chlorophyll Nutrition 0.000 description 1
- ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 229940090961 chromium dioxide Drugs 0.000 description 1
- 238000005253 cladding Methods 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 239000000112 cooling gas Substances 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 150000004696 coordination complex Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- TVZPLCNGKSPOJA-UHFFFAOYSA-N copper zinc Chemical compound [Cu].[Zn] TVZPLCNGKSPOJA-UHFFFAOYSA-N 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- PPSZHCXTGRHULJ-UHFFFAOYSA-N dioxazine Chemical compound O1ON=CC=C1 PPSZHCXTGRHULJ-UHFFFAOYSA-N 0.000 description 1
- VAPILSUCBNPFBS-UHFFFAOYSA-L disodium 2-oxido-5-[[4-[(4-sulfophenyl)diazenyl]phenyl]diazenyl]benzoate Chemical compound [Na+].[Na+].Oc1ccc(cc1C([O-])=O)N=Nc1ccc(cc1)N=Nc1ccc(cc1)S([O-])(=O)=O VAPILSUCBNPFBS-UHFFFAOYSA-L 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
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- 230000007717 exclusion Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 230000004992 fission Effects 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 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 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229940097275 indigo Drugs 0.000 description 1
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- DCYOBGZUOMKFPA-UHFFFAOYSA-N iron(2+);iron(3+);octadecacyanide Chemical compound [Fe+2].[Fe+2].[Fe+2].[Fe+3].[Fe+3].[Fe+3].[Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] DCYOBGZUOMKFPA-UHFFFAOYSA-N 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- PXZQEOJJUGGUIB-UHFFFAOYSA-N isoindolin-1-one Chemical compound C1=CC=C2C(=O)NCC2=C1 PXZQEOJJUGGUIB-UHFFFAOYSA-N 0.000 description 1
- 239000002346 layers by function Substances 0.000 description 1
- MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- DGBWPZSGHAXYGK-UHFFFAOYSA-N perinone Chemical compound C12=NC3=CC=CC=C3N2C(=O)C2=CC=C3C4=C2C1=CC=C4C(=O)N1C2=CC=CC=C2N=C13 DGBWPZSGHAXYGK-UHFFFAOYSA-N 0.000 description 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 239000006223 plastic coating Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
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- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
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- 238000002203 pretreatment Methods 0.000 description 1
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- 238000003908 quality control method Methods 0.000 description 1
- 238000003847 radiation curing Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000012763 reinforcing filler Substances 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000035943 smell Effects 0.000 description 1
- FPSFKBGHBCHTOE-UHFFFAOYSA-N sodium 3-hydroxy-4-[(3-methyl-5-oxo-1-phenyl-4H-pyrazol-4-yl)diazenyl]naphthalene-1-sulfonic acid Chemical compound [Na+].O=C1C(N=NC=2C3=CC=CC=C3C(=CC=2O)S(O)(=O)=O)C(C)=NN1C1=CC=CC=C1 FPSFKBGHBCHTOE-UHFFFAOYSA-N 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- NVKTUNLPFJHLCG-UHFFFAOYSA-N strontium chromate Chemical compound [Sr+2].[O-][Cr]([O-])(=O)=O NVKTUNLPFJHLCG-UHFFFAOYSA-N 0.000 description 1
- 239000001040 synthetic pigment Substances 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- 230000008542 thermal sensitivity Effects 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 239000004924 water-based lacquer Substances 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- NDKWCCLKSWNDBG-UHFFFAOYSA-N zinc;dioxido(dioxo)chromium Chemical compound [Zn+2].[O-][Cr]([O-])(=O)=O NDKWCCLKSWNDBG-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F26—DRYING
- F26B—DRYING SOLID MATERIALS OR OBJECTS BY REMOVING LIQUID THEREFROM
- F26B3/00—Drying solid materials or objects by processes involving the application of heat
- F26B3/28—Drying solid materials or objects by processes involving the application of heat by radiation, e.g. from the sun
- F26B3/30—Drying solid materials or objects by processes involving the application of heat by radiation, e.g. from the sun from infrared-emitting elements
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F26—DRYING
- F26B—DRYING SOLID MATERIALS OR OBJECTS BY REMOVING LIQUID THEREFROM
- F26B3/00—Drying solid materials or objects by processes involving the application of heat
- F26B3/28—Drying solid materials or objects by processes involving the application of heat by radiation, e.g. from the sun
Definitions
- the invention relates to a method for producing a coating by means of electromagnetic radiation on a quasi-endlessly conveyed, in particular band-shaped, flexible material band moving in the conveying direction.
- Coatings of surfaces not only play a role with regard to the aesthetic effect, but also serve, for example, to protect a certain object against external influences, e.g. to make it more resistant to light radiation, water, heat and mechanical influences.
- the coating can impart physical properties that the body to be coated does not have per se, such as electrical conductivity or magnetizability.
- Quasi-endless coated metal sheets in particular steel and aluminum sheets, are used in huge quantities in the automotive industry and also for the manufacture of household appliances (the so-called white goods) and also for the manufacture of air and water vehicles and cladding for the building industry processed.
- the steel sheets are primarily bare, galvanized or nickel-plated (steel) sheets with thicknesses in the range between a few tenths of a millimeter and over a millimeter.
- Such sheets are Coils are wound up on rolls before they are continuously fed to a specific forming or stamping process.
- the sheets already have an anti-corrosion coating and / or a primer or a coating on the coil primer application.
- these metal strips are coated before the process step of bending, embossing, etc., in which the sheet is ultimately brought into the desired shape.
- at least one coating agent is usually rolled on at a first station of this system or applied to the metal strip using another technique.
- Such coating compositions are mostly applied in the liquid state, but occasionally also as a powder coating.
- the metal strip Since the coating agent must be completely dried or crosslinked before the subsequent process steps, the metal strip is subsequently fed to an oven, which often works on the principle of forced air drying. In this furnace, the coating agent is heated together with the entire sheet of the metal strip, so that the coating agent dries and / or cross-links. Due to the strong heating of the metal strip, cooling of the metal strip is necessary after the drying process. Since the metal strip is often subjected to bending, embossing and welding processes after the coating process, particularly high demands are placed on the quality of the dried or crosslinked coating agent. So it must not flake off when bending or embossing. Furthermore, the coated metal strip must remain weldable.
- the thermal energy required for drying or crosslinking the coating agent is transferred inductively, ie by means of electromagnetic coupling, to the metal strip. That so heated metal strip releases the thermal energy to the coating agent by thermal conduction, as a result of which it is dried or crosslinked.
- the entire metal strip must be heated from the ambient temperature outside the system to at least the temperature required for drying or crosslinking the coating agent.
- the metal strip in the case of a coating agent which requires a temperature of 180 ° C. for crosslinking, the metal strip must be heated inductively to approximately 250 ° C. in order to produce a sufficient temperature gradient between the metal strip and the coating agent, so that the coating agent is in one acceptable time can be dried or crosslinked.
- Thin-film structures on large, thin, quasi-endlessly conveyed material belts or carriers are also becoming increasingly important in various fields of technology.
- thin-film transistor structures such as are used in particular in liquid crystal display arrangements, and other thin-film systems for display units, for example for plasma displays.
- Other technically and economically important thin-film structures are the separator structures of electrochemical elements, in particular primary or secondary elements based on lithium (lithium batteries and lithium-ion batteries etc.) as well as highly differentiated membrane systems for material separation and energy generation, for example in fuel cells.
- a thin coating applied to a thin carrier in an initial state usually has to be converted into a functional layer and firmly connected to the carrier. The important thing here is to realize a process with a very high degree of reliability and excluding damage to the carrier or the coating material with a high productivity, ie a high area throughput per unit of time.
- This object is achieved according to the invention by a method for producing a coating according to the features of claim 1 and by a device according to the features of claim 16.
- Advantageous embodiments of the invention are the subject of the dependent claims.
- the present invention thus relates to a method for producing a coating of quasi-endless, conveyed and conveyed material belts which are provided with a coating agent which is at least partially dried and / or crosslinked at least partially by means of electromagnetic radiation, the essential one Active component of the electromagnetic radiation is in the wavelength range of the near infrared.
- the present invention relates in particular to a method for producing a coating or a thin layer structure from a band-shaped, flexible, in particular quasi-endless, carrier with at least one functional coating connected to the carrier, which has a thickness that is in particular of the order of the thickness of the carrier has the steps of forming an output layer structure by surface-coating a coating agent on the carrier and irradiating the carrier provided with the coating agent with electromagnetic radiation, which has an active component in the near infrared range, to form the functional coating from the Coating agent with simultaneous connection to the carrier including drying and / or thermal crosslinking.
- An important application of the proposed method is in particular the drying and / or crosslinking of an anti-corrosion agent or a primer or a primer for subsequent painting, in particular on the surface of a bare, galvanized or nickel-plated steel sheet, in particular for automobile or household appliance production (coil coating).
- the coating agent in the initial state is a powder or liquid lacquer layer which is dried or crosslinked to give an intermediate or final lacquer.
- the method according to the invention is characterized by potentially high productivity, simplicity and reliability with extensive exclusion of damage to the coating (s) and / or the carrier.
- the method according to the invention it is possible to coat on a material strip with particularly short irradiation times, preferably in less than 30s, preferably in less than 10s, more preferably less than 5 s, in particular 2s, and therefore compared to a conventional coating or Coil coating process, particularly quick to produce. Due to the short treatment or irradiation time, the material strip is subjected to little thermal stress. sprucht. This makes it possible to coat thermally sensitive materials such as thermoplastics with coating agents that require temperatures for crosslinking that are higher than the damage temperature of the material strip. Thus, the method according to the invention makes it possible, in particular, to coat strips of material whose coating was previously not possible due to their thermal sensitivity or only with great technical difficulties.
- Changes in the material structure and / or changes in material properties can also be avoided by applying the method according to the invention, which was often not possible with conventional methods, or only if the time required to carry out the method was considerably extended.
- strips of material can be coated, the microscopic structure of which changes when heat is applied (which can reduce their mechanical strength properties or structural changes in the material), e.g. Aluminum or alloys, or strips of material, the materials of which segregate, e.g. Composites.
- the intensity maximum or the spectral composition of the electromagnetic radiation is adapted to the absorption and transmission properties of the coating agent and, optionally, of the material strip.
- the wavelength of the maximum intensity and or the spectral composition of the electromagnetic radiation is preferably selected so that the coating
- the radiation energy is absorbed substantially uniformly over its layer thickness, an inadmissible thermal load on the carrier and also individual areas of the coating being avoided. It can thereby be achieved that the coating agent is at least partially heated and / or crosslinked directly and at least partially by the radiation within a very short time.
- the spectral composition of the electromagnetic radiation is preferably set by at least one filter.
- the intensity maximum of the electromagnetic radiation can preferably be set so that relatively little radiation is absorbed in the material band in order to avoid useless heating thereof. Due to the very short irradiation times, an energy transfer by heat conduction, which takes place slowly in comparison to the energy transfer by radiation, can be greatly reduced to the material strip in contact with the coating agent.
- a clear temperature gradient in the material strip and thus an energy separation between the material strip and the coating agent to be dried or crosslinked are achieved.
- a significantly higher degree of efficiency can be achieved in comparison to conventional methods, and the amount of energy required to carry out the method according to the invention can be considerably reduced compared to conventional methods, depending on the material properties, such as the specific heat capacity, the thickness of the material strip or the coating material , because comparatively little thermal energy is transferred to the material belt.
- This effect is particularly important for materials with a particularly high heat capacity, such as sheet steel, since these materials require a large amount of energy absorb.
- the heating of the sheet from 250 ° C. can be reduced to 200 ° C. Accordingly, this means a reduction in the energy expenditure required for drying or crosslinking the coating agent by a fifth. Larger temperature differences, ie energy savings, are also possible with thicker materials.
- the surface of the material strip is preferably treated for the purpose of specifically adjusting its reflectivity before the coating agent is actually applied. This is done, for example, by smoothing, polishing or roughening the surface.
- the intensity maximum of the electromagnetic radiation is adapted to the absorption and / or transmission properties of the material band in such a way that the electromagnetic radiation at least partially penetrates the material band.
- This is particularly useful when the coating agent is applied to both sides of the material strip.
- certain coating agent / material strip combinations can be used the drying or crosslinking is carried out in such a way that the electromagnetic radiation used for drying or crosslinking, in addition to the coating agent which is applied to the material strip side facing the radiation source, also penetrates the material strip.
- no radiation energy is preferably absorbed in the material band.
- electromagnetic radiation is only applied from one side of the material strip.
- the coating agent applied to the material strip on both sides is dried or crosslinked essentially simultaneously on both sides of the material strip.
- the method according to the invention can be carried out in such a way that the coating agent applied on both sides is dried or crosslinked essentially simultaneously with a radiation source which is arranged on only one side of the material strip and has at least one emitter.
- the method according to the invention in an application in which the coating agent is applied on one side but on the side facing away from the radiation source.
- the electromagnetic radiation preferably penetrates the material strip, essentially without being absorbed by it, in order then to dry or crosslink the coating agent.
- the radiation source can be protected from the volatile and highly flammable components emerging from the coating agent by the material strip and / or one or more further processing steps can be carried out simultaneously with the irradiation process on the side of the material strip to which the coating agent is applied the coating agent and / or the material strip can be carried out without impeding the irradiation process.
- the drying or crosslinking processes of the coating agent are essentially thermal.
- energy is transferred to the coating agent, which is used in the form of thermal energy to cause the formation of polymer chains.
- a certain temperature of the coating composition is required for the crosslinking process to take place.
- coating agents are dried or crosslinked essentially completely by photoreactions, while thermal processes play only a minor role or not at all.
- the coating agent can be dried or crosslinked either completely or only partially by means of the electromagnetic radiation, the essential active component of which lies in the wavelength range of the near infrared. However, it is also possible to dry or crosslink the coating agent in a plurality of time intervals which are separated or offset from one another. Drying or crosslinking can also be supported at the same time or at different times from the above-mentioned radiation by at least one additional radiation source, in particular with an active component in a different wavelength range, and / or by at least one other energy or heat source.
- the radiation field of the electromagnetic radiation in a proven and cost-effective manner according to the invention is preferred by at least one thermal one Radiant body or emitter generated, the radiator temperature is above 2900 K and preferably above 3200 K.
- electromagnetic radiation with a high power density is preferably used.
- Typical power densities characteristic of the method according to the invention are in particular above 100 kW / m 2 , preferably above 200 kW / m 2 and particularly preferably above 500 kW / m 2 .
- Such high power densities can be achieved, for example, by the arrangement of a plurality of interacting, in particular parallel, halogen lamps which extend over the entire width of the moving material strip and have correspondingly assigned highly effective reflectors.
- a further adjustment of the power density can be achieved in that, according to the present invention, the electromagnetic radiation is focused on the surface of the material strip provided with the coating agent.
- the power density can also be set via the operating voltage; Filters can also be used.
- power control is provided on the basis of feedback sensor signals (for example temperature sensors).
- an electromagnetic radiation the intensity maximum of which lies in the wavelength range from 0.8 ⁇ m to 2 ⁇ m.
- Such a wavelength range of the electromagnetic radiation has proven to be particularly effective for a highly effective polymer formation or polymer crosslinking of the coating agents used for coating material strips.
- the invention preferably enables the above-mentioned short irradiation times for specific material strips and / or coating agents for optimal power densities to be determined.
- pre-treatment of the material strip is often provided before application.
- heating of the material strip is necessary.
- Steel sheet usually has to be heated to temperatures of 900 ° C to 1100 ° C to achieve a structural change, which is usually carried out under an inert atmosphere or hydrogen atmosphere.
- methods using convection or induction heating are used for this.
- the processes in which convection heating is used take a long time to heat the steel strip to the high temperature. Efficiency and homogeneous heating are problematic in induction heating.
- this preheating is likewise effected by means of electromagnetic radiation, the essential active component of which lies in the wavelength range of the near infrared. This makes it possible to heat the steel strip much faster than with conventional methods based on slow heat conduction.
- the electromagnetic radiation used for this preferably has its essential active component likewise in the wavelength range from 0.8 ⁇ m to 2.0 ⁇ m.
- the wavelength is preferably adjusted so that a large part of the electromagnetic radiation is absorbed by the material band.
- At least one measurable process parameter is used, which allows a conclusion to be drawn about the condition and quality of the coating by means of a corresponding automated process control.
- the temperature is particularly suitable for this the surface of the material band, which can be changed on the one hand by a corresponding change in the electrical power and thus the radiation power of the emitter and on the other hand by varying the distance between the emitters and the surface of the material band.
- a device for realizing a possibly automatic setting of radiation parameters comprises at least one sensor for detecting the relevant physical quantities, in particular one or more photoelectric sensors for detecting the brightness, the reflectivity or the refractive index or other optical parameters which provide information about the Provide the drying or crosslinking state of the coating agent, or a contactless, in particular pyrometric temperature sensor.
- the sensor or the sensors is connected to a control input or control inputs of a radiation control device via an evaluation circuit.
- the radiation parameters to be set in the further course of the process in particular the power density and possibly the spectral composition of the radiation, can be optimized.
- an automatically controlled real-time operational management can also be implemented.
- cooling and / or removal of these volatile constituents is also carried out by means of a gas flow, preferably at right angles to the conveying direction, along the latter, in particular air flow. meaningful.
- This gas stream sweeping over the material strip preferably strikes the material to be removed at a certain predetermined speed
- the Gas flow preferably impinges knife-like on the material to be dried.
- a dry, cold gas with high momentum is supplied.
- a gas flow sweeping over the surface of the applied coating agent and / or the rear surface of the carrier can, on the one hand, achieve a uniform distribution of the temperature and, if necessary, lower the surface temperature, and on the other hand can quickly remove volatile constituents of the coating agent. This further increases the reliability and efficiency of the method.
- the gas stream (air stream) is preferably dry and cold and is supplied at high pressure or pulse. Further details in this regard are disclosed in DE-A 198 07 643 by the applicant.
- the endlessly conveyed material band is preferably a metal band, in particular a steel band.
- the endlessly conveyed material band can, however, also be metal foils or fine metal mesh, especially made of aluminum or copper or their alloys or made of an alloy containing aluminum or copper, plastic foils, especially polyethylene (PE), polypropylene (PP) or PVC films, around glass layers or sheets, around material composite systems, such as Wood veneers to laminates such as Capacitors or displays, or thermoplastics or thermosets.
- Other preferred areas of application are films for packaging, such as Blister films or adhesive films.
- both the coating agent and the material band or the carrier have an average thickness in the range between 5 ⁇ m and 500 ⁇ m, in particular between 20 ⁇ m and 200 ⁇ m.
- the coating agent and the solid thin layer formed therefrom have a thickness in the range between l ⁇ m and lOO ⁇ m, in particular between 2 ⁇ m and 20 ⁇ m.
- the coating agent is applied to the material strip to be coated depending on the nature, in particular the surface and / or the material composition of the material band.
- the coating agent is preferably applied as a fluid or pasty system, which can be accomplished using known application methods, in particular by rolling on, spreading on, spraying on, pouring, spinning on, trickling on, inflating or knife coating.
- the coating composition is applied in the form of a powder, in particular using electrostatic forces, in particular sprinkled on or inflated.
- it can also be sputtered onto the material tape.
- a pretreatment in particular by roughening, etching or also by applying an adhesion promoter, may be appropriate. This pretreatment serves, inter alia, to improve the adhesion between the coating agent and the material strip moving in the conveying direction.
- coatings paints, in particular powder coatings, one-component or two-component wet coatings, both water-based and based on organic solvents, coatings for corrosion protection, coatings for pretreatment and for the functionalization of metal surfaces, conductivity pastes and photoresist.
- paints are substances that are at least partially dryable and / or crosslinkable with radiation.
- Paint systems are typically systems that contain at least one additive, preferably one additive and one binder, as discussed in detail below. In many paints, radiation curing often takes place by polymerizing the binder contained in the paint.
- wet lacquers or powder lacquers can be used for the process according to the invention. Water-based paints and solvent-based paints are referred to as wet paints.
- Wet lacquers can be one-component lacquers, such as UV lacquers, and two-component lacquers, it being possible to use water-based lacquers or else based on organic solvents. Combinations of these are also conceivable for multilayer structures.
- weldable coating systems are also of interest for the above-mentioned coil coating processes.
- solvent-based paints are divided into conventional, solvent-based paints, low-solvent and solvent-free paints.
- the solids content of low-solvent paints is greater than 70% by mass; with a solids content of less than 70 mass% one speaks of solvent-based paints.
- the term high-solids is also used for high-solids paints such as spray paints.
- Low-solvent and solvent-free lacquers are divided into one and two-component systems according to the type of curing reaction.
- one-component paints the polymerization and thus the crosslinking commence after the addition of initiators and accelerators or through the action of UV or electron beams.
- vinyl chloride polymers or copolymers and unsaturated polyester resins such as low molecular weight hydroxyl-bearing acrylate, alkyd and polyester resins are used as one-component paints.
- Two-component paints harden through an addition reaction, in which, in contrast to the one-component paints, no environmentally harmful fission products are released.
- the binders are usually epoxy resins in combination with hardeners or polyisocyanates in combination with hydroxyl-containing resins.
- Powder coatings are thermoplastic or thermosetting plastics that are applied in powder form to substrates.
- Application methods such as electrostatic powder spraying, electrostatic whirl sintering, bulk sintering, whirl sintering, rotary sintering or centrifugal casting are used.
- epoxy resin powder, powder of saturated polyester resins, polyacrylate powder, polyethylene powder, polyvinyl chloride powder, polyamide powder, cellulose acetate butyrate powder, chlorinated polyether, ethylene-vinyl acetate mixed polymer powder or polymethacrylic acid methyl ester powder are used as powder coatings.
- UV lacquers require a so-called UV initiator, which is an expensive component of the lacquer, but is necessary for crosslinking.
- UV initiators can be dispensed with in many cases, but UV lacquers of this type can nevertheless be dried using the method according to the invention.
- binders which can be crosslinked by radiation-induced processes in the process according to the invention. They are either binders that can be crosslinked by radical polymerization or can be crosslinked by cationic polymerization. In the former, radicals are generated by the action of electromagnetic radiation on the binders then trigger the crosslinking reaction. In the case of the cationically curing systems, Lewis acids are formed by the irradiation from initiators, which then trigger the crosslinking reaction.
- additives such as polymers, in particular crosslinking agents, catalysts for crosslinking, initiators, in particular pigments, dyes, fillers, reinforcing fillers, rheology aids, wetting and dispersing agents, adhesion promoters, additives for improving the surface wetting, additives for improving the surface smoothness , Matting agents, leveling agents, film-forming aids, drying agents, skin-preventing agents, light stabilizers, corrosion inhibitors, biocides, flame retardants, polymerization inhibitors, in particular photoinhibitors or plasticizers, as are customary and known, for example, in the paint industry.
- additives such as polymers, in particular crosslinking agents, catalysts for crosslinking, initiators, in particular pigments, dyes, fillers, reinforcing fillers, rheology aids, wetting and dispersing agents, adhesion promoters, additives for improving the surface wetting, additives for improving the surface smoothness , Matting agents, leveling agents, film-forming aids, drying
- the coating compositions can also contain ceramic colors, such as titanium dioxide, carbon black or colored pigments such as lead chromate, red lead, zinc yellow, zinc green, cadmium red, cobalt blue, Berlin blue, ultramarine, manganese violet, cadmium yellow, molybdenum orange and red, chrome orange and red, iron oxide red, chromium dioxide green and strontium yellow.
- ceramic colors such as titanium dioxide, carbon black or colored pigments such as lead chromate, red lead, zinc yellow, zinc green, cadmium red, cobalt blue, Berlin blue, ultramarine, manganese violet, cadmium yellow, molybdenum orange and red, chrome orange and red, iron oxide red, chromium dioxide green and strontium yellow.
- organic colors for example naturally occurring pigments such as sepia, indigo, chlorophyll, or in particular synthetic pigments such as for example azo pigments, indigoids, dioxazine, cliinacridone, phthalocyanine, isoindolidone, perylene and perinone, metal complex and alkali blue Pigments can be components of the coating compositions.
- the coating compositions can also contain luminescent pigments to produce a metallic effect.
- Metal platelets can be used in particular, preferably aluminum plates, which give a special optical effect through their reflection behavior.
- Other metal platelets are, for example, those based on gold bronzes, copper-zinc alloys, nickel, stainless steel and mica.
- the coating compositions can also contain luminescent pigments for producing metamerism effects.
- pigments can be used to create a pearlescent sheen.
- bismuth oxide chloride, titanium dioxide mica and lead carbonate are to be found.
- the coating compositions can contain pigments with high reflectivity for IR radiation, in particular lead carbonate and titanium dioxide mica. Destructive interference leads to the extinction of essential radiation components, whereby thermal protection is achieved.
- the coating compositions can also contain pigments for corrosion protection.
- Lead (II) orthoplumbate, chromate pigments, phosphate pigments, zinc dust or lead dust are preferably used.
- the coating compositions can contain magnetic pigments such as pure iron, iron oxide or chromium (IV) oxide.
- the proposed method is particularly suitable for the production of a functional coating for the production of thin-film transistor arrangements, in particular for liquid crystal display arrangements, of separator membranes for electrochemical elements, in particular of lithium-ion batteries, for the production of thin-film structures for plasma displays and for the production of membrane structures for fuel cells.
- a coated substrate which has a substrate and a dried and / or crosslinked coating agent which is applied on one or both sides.
- the substrate is selected in particular from a thermoplastic substrate, a metal foil or sheet, a plastic film, a glass plate, a composite material system such as a wood veneer, a laminate such as capacitors or displays.
- the coating agent is preferably selected from a lacquer, in particular powder lacquer, a one-component or two-component wet lacquer, both water-based and organic solvent-based, a coating for corrosion protection, a coating for pretreatment and for the functionalization of metal surfaces, a conductivity paste or a photoresist ,
- the radiation device is preferred. device designed as a
- a means for setting or a regulating device for regulating the radiation power in particular adjusting means for precision adjustment of at least one radiation source of the irradiation device, is provided.
- the method according to the invention is preferably carried out using a device which has an essentially closed device through which the material strip provided with a coating agent is conveyed on one or both sides, in which at least one emitter is mounted and the inner walls of which are equipped with at least one electromagnetic one Radiation reflecting device, such as are provided with a reflector.
- the side reflectors can be adjusted, for example by means of displacement devices, and can be adapted to the width of the material strip to be coated while forming the radiation space.
- the width of the radiation space can be adapted to the width of the material strip and the efficiency of the system can be optimized independently of the width of the material strip.
- the emitters located outside the supplied side reflectors are not used. In this way, optimal and thus energy-saving drying or crosslinking of the coating agent can always be achieved.
- Such an adjustment Solution of the energy sources used for drying or for crosslinking is not possible with conventional methods and is a major problem.
- the electromagnetic radiation used for drying or crosslinking can be selected so that in addition to the coating agent, the material strip can also be penetrated by the radiation, it is sensible for investment reasons to arrange emitter modules only on one side of the material strip.
- the device has at least one emitter, which in particular contains a thermal radiating body, in particular an incandescent lamp or a halogen lamp, which is operated in particular at an increased operating temperature.
- the emitter is provided by a tube radiator formed with a filament extending in a radiation-permeable tube, in particular in a quartz glass tube, as a thermal radiant body.
- thermal radiation body instead of the thermal radiation body, alternative radiation sources such as laser diodes, plasma emitters, UV emitters or radiation sources based on other physical effects can also be used. If necessary, it is also possible to arrange a plurality of emitters, preferably parallel to one another, as so-called emitter modules over the entire width of the material band moving rapidly in the conveying direction.
- the emitters are arranged parallel to the conveying direction of the endlessly conveyed material band. This has the essential advantage that the irradiance remains homogeneous over the entire material band, both in the conveying direction and in the direction perpendicular to it, even if, for example, the aging process of the emitters or another effect changes the radiation homogeneity along the longitudinal direction of the emitters , assuming that this change is the same for all emitters.
- a special linear arrangement of the emitters is selected for the irradiation of linearly, for example, lattice-shaped, endlessly conveyed material belts in the conveying direction, so that in each case an emitter or is arranged essentially parallel to a material part of the lattice-like material belt arranged parallel to the conveying direction optionally a series of emitters arranged one behind the other.
- the radiation emitted by the emitters can be focused on the material parts by appropriate reflective devices.
- the arrangement of a reflector on the side opposite the material strip in relation to the emitters is desirable in order to increase the efficiency of the system.
- linear emitters oriented transversely to the conveying direction are additionally provided which can be moved with the material parts at their conveying speed. Further details of this special embodiment can be found in one of the applicants under the title “Method and device for heating continuously conveyed, lattice-like material or similar structures "with the application number DE 10062633 filed application.
- a quartz glass pane This can prevent solvents from igniting due to the high temperatures on the outer surface of the emitter body.
- two quartz glass panes arranged next to one another are provided between the material band and the emitter or emitters, between which an additional cooling gas, e.g. Nitrogen gas flows to prevent heating of the solvent more effectively.
- a gas flow generating device for generating and aligning the above-mentioned gas flow and / or a device for power adjustment or control is additionally provided, the latter preferably comprising means for adjusting the distance between the radiation source and the layer structure.
- the gas flow generating device is preferably designed in such a way that a gas pulse which is directed essentially parallel to the surface of the material strip and which passes over the irradiation device, particularly dry and cold gas flow, is generated with a high pulse.
- FIG. 1 shows a sketch of a coil coating device 1 for coating a quasi-endless steel sheet 3, which is wound onto a coil 5, and for drying the coating.
- the coil 5 is set in rotation by an electric drive 7, and the sheet 3 is thereby moved under a spray coater 9 and an NIR drying section 11.
- the spray coater 9 applies an aqueous solution 13 'to the sheet 3 as a starting material for a corrosion protection or primer layer 13. This is dried in an elongated radiation zone A formed by the NIR drying section 11 with NIR radiation having a high power density, in particular above 500 kW / m 2 .
- the NIR drying section 11 comprises a solid Al reflector 15 with a plurality of reflector sections 15a which are approximately W-shaped in cross section and which are internally water-cooled and, for this purpose, connected to an external cooler (not shown) via cooling water lines 17.
- each reflector section 15a is an elongated tubular halogen filament lamp 19.
- each elongated halogen lamp is assigned a reflector section with a partially elliptical, partially parabolic or essentially W-shaped cross section.
- the halogen filament lamps 19 are supplied with current by an irradiation control unit 21 and controlled in such a way that they emit NIR radiation with an intensity maximum in the range between 0.8 ⁇ m and 1.5 ⁇ m with a radiator temperature above 2900 K.
- the radiation control device assigned to the radiation device is preferably suitable for setting the power density of the radiation on the surface of the coating agent to a value of more than 500 kW / m 2 , in particular more than 750 kW / m 2 , and / or for setting the temperature in the layering agent to a value above 200 ° C, in particular to a value in the range between 200 and 250 ° C.
- a pyrometer element 23 for detecting the surface temperature of the coating 13 in a T-detection zone B, which is connected to a signal input of the radiation control unit 21.
- the radiation is controlled in such a way that an essentially constant temperature is maintained in the coating, which temperature is selected as a function of the physical and chemical properties of the starting material 13 ′ of the corrosion protection or primer layer 13 and is typically around 200 ° C.
- the throughput speed of the steel sheet 13 through the irradiation zone A is set such that a residence time of the aqueous solution 13 'in the irradiation zone A of a few seconds is obtained, which is necessary for the complete evaporation of the solvent component and for the thermal crosslinking of the layer 13 is sufficient.
- the sheet is typically conveyed through the drying device at a speed in the range between 50 and 200 m / min, in particular between 75 and 150 m / min.
- Irradiation device with a length of 2 to 5 meters and more than one megawatt, preferably 2 to 5 MW, to use power consumption which has a radiation power density of more than 500 kW / m 2 , in particular more than 750 kW /, on the surface of the coating to be dried or crosslinked. m 2 .
- the method preferably does not require an active gas flow supply to remove evaporating coating components; essentially convection over the heated coating is used for this purpose.
- an active gas flow supply to remove evaporating coating components
- a gas stream sweeping over the surface in particular an air stream generated by a suitable fan, can certainly be used.
- At least one process-relevant physical variable of the coating system is preferably measured and evaluated for process control.
Abstract
Description
Claims
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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DE10109847A DE10109847A1 (en) | 2001-03-01 | 2001-03-01 | Method for producing a coating on a quasi-endlessly conveyed material belt |
DE10109847 | 2001-03-01 | ||
PCT/EP2002/002280 WO2002070973A1 (en) | 2001-03-01 | 2002-03-01 | Method for producing a coating on a quasi-continuously fed material strip |
Publications (3)
Publication Number | Publication Date |
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EP1366331A1 true EP1366331A1 (en) | 2003-12-03 |
EP1366331B1 EP1366331B1 (en) | 2010-11-24 |
EP1366331B2 EP1366331B2 (en) | 2014-12-31 |
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EP02702389.4A Expired - Lifetime EP1366331B2 (en) | 2001-03-01 | 2002-03-01 | Method for producing a coating on a quasi-continuously fed material strip |
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Country | Link |
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EP (1) | EP1366331B2 (en) |
AT (1) | ATE489594T1 (en) |
DE (2) | DE10109847A1 (en) |
WO (1) | WO2002070973A1 (en) |
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DE102005043075A1 (en) * | 2005-09-10 | 2007-03-15 | Rehau Ag + Co. | Process for drying a paint layer applied to a motor vehicle component and drying system therefor |
DE102008029580A1 (en) * | 2008-06-21 | 2009-12-24 | Basf Coatings Ag | Producing coatings, useful for coating a substrate e.g. metal band, comprises applying electron radiation curable, coating composition on substrate, heating the composition on the substrate and curing the composition by electron radiation |
DE102019101522A1 (en) * | 2019-01-22 | 2020-07-23 | Koenig & Bauer Ag | Process for coating a web-shaped substrate and device for carrying out the process |
DE102019114806A1 (en) * | 2019-06-03 | 2020-12-03 | Value & Intellectual Properties Management Gmbh | Process for the production of electrical or electronic components or circuits on a flexible flat carrier |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB771969A (en) † | 1954-09-27 | 1957-04-10 | Rudolf Pabst | Improvements in or relating to an advertising device |
US3286369A (en) * | 1963-03-04 | 1966-11-22 | Hupp Corp | Drying apparatus |
LU84911A1 (en) * | 1983-07-14 | 1985-04-17 | Cockerill Sambre Sa | METHOD AND INSTALLATION FOR COOKING AN ORGANIC COATING APPLIED TO A SUPPORT |
DE3828753C2 (en) † | 1988-08-25 | 1994-05-19 | Heidelberger Druckmasch Ag | Device for drying printed products in a printing press |
EP0378731B1 (en) * | 1989-01-20 | 1993-01-07 | Ching-Shun Wu | Varnishing furnace |
EP0486035B1 (en) * | 1990-11-16 | 1995-02-01 | Setsuo Tate | Drying method and devices for coated layer |
DE4229352A1 (en) † | 1992-09-07 | 1994-04-14 | Bhs Bayerische Berg | Printing press |
DE4339661C2 (en) † | 1993-11-22 | 1996-09-26 | Fraunhofer Ges Forschung | Process for the production of tubular blanks from thin or very thin sheet |
DE4435077A1 (en) † | 1994-09-30 | 1995-11-09 | Siemens Nixdorf Inf Syst | Rapidly switchable, high speed infrared fixing of toner images in electrographic printer or copier |
CA2222047A1 (en) * | 1996-04-18 | 1997-10-23 | Infrarodteknik Ab | Method and device for drying a moving web material |
AU6316498A (en) * | 1997-01-15 | 1998-08-07 | Optimum Air Corporation | System and method for drying and curing waterbased coatings |
US6026748A (en) † | 1997-11-11 | 2000-02-22 | Oxy-Dry Corporation | Infrared dryer system for printing presses |
DE19811134A1 (en) † | 1998-03-16 | 1999-09-23 | Lemo Maschb Gmbh | Flexographic printing machine with several individually driven printing units |
KR20000011746A (en) * | 1998-07-17 | 2000-02-25 | 미야무라 심뻬이 | Method of drying copper foil and copper foil drying apparatus |
JP3735769B2 (en) * | 1998-07-30 | 2006-01-18 | 大東製機株式会社 | Drying device, drying device assembly and drying method |
DE19857045C2 (en) * | 1998-12-10 | 2001-02-01 | Industrieservis Ges Fuer Innov | Coating of objects |
DE20020691U1 (en) * | 2000-08-09 | 2001-02-22 | Advanced Photonics Tech Ag | Device for drying inkjet prints |
-
2001
- 2001-03-01 DE DE10109847A patent/DE10109847A1/en not_active Withdrawn
-
2002
- 2002-03-01 EP EP02702389.4A patent/EP1366331B2/en not_active Expired - Lifetime
- 2002-03-01 AT AT02702389T patent/ATE489594T1/en active
- 2002-03-01 DE DE50214786T patent/DE50214786D1/en not_active Expired - Lifetime
- 2002-03-01 WO PCT/EP2002/002280 patent/WO2002070973A1/en not_active Application Discontinuation
Non-Patent Citations (1)
Title |
---|
See references of WO02070973A1 * |
Also Published As
Publication number | Publication date |
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EP1366331B2 (en) | 2014-12-31 |
ATE489594T1 (en) | 2010-12-15 |
EP1366331B1 (en) | 2010-11-24 |
DE10109847A1 (en) | 2002-09-19 |
WO2002070973A1 (en) | 2002-09-12 |
DE50214786D1 (en) | 2011-01-05 |
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