EP1112126B1 - Verfahren zur herstellung zweischichtiger automobildecklackierungen - Google Patents
Verfahren zur herstellung zweischichtiger automobildecklackierungen Download PDFInfo
- Publication number
- EP1112126B1 EP1112126B1 EP00907551A EP00907551A EP1112126B1 EP 1112126 B1 EP1112126 B1 EP 1112126B1 EP 00907551 A EP00907551 A EP 00907551A EP 00907551 A EP00907551 A EP 00907551A EP 1112126 B1 EP1112126 B1 EP 1112126B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- basecoat
- aqueous
- waterborne
- coat layer
- organic solvents
- 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.)
- Expired - Lifetime
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 238000000034 method Methods 0.000 claims abstract description 32
- 239000004922 lacquer Substances 0.000 claims abstract description 18
- 239000011248 coating agent Substances 0.000 claims abstract description 14
- 238000000576 coating method Methods 0.000 claims abstract description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 27
- 239000010410 layer Substances 0.000 claims description 24
- 239000003960 organic solvent Substances 0.000 claims description 21
- 239000007787 solid Substances 0.000 claims description 17
- 238000010422 painting Methods 0.000 claims description 16
- 239000011247 coating layer Substances 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- 238000009835 boiling Methods 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims 4
- 238000009434 installation Methods 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- 239000008199 coating composition Substances 0.000 abstract description 7
- 239000003570 air Substances 0.000 description 38
- 239000000049 pigment Substances 0.000 description 23
- 239000003973 paint Substances 0.000 description 21
- 239000011230 binding agent Substances 0.000 description 17
- 230000000694 effects Effects 0.000 description 15
- 238000009423 ventilation Methods 0.000 description 11
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 8
- 239000000945 filler Substances 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 6
- 239000000758 substrate Substances 0.000 description 5
- 239000004971 Cross linker Substances 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000004408 titanium dioxide Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 239000010445 mica Substances 0.000 description 3
- 229910052618 mica group Inorganic materials 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 238000013022 venting Methods 0.000 description 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 2
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 239000006259 organic additive Substances 0.000 description 2
- 239000012860 organic pigment Substances 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 239000004924 water-based lacquer Substances 0.000 description 2
- LEEANUDEDHYDTG-UHFFFAOYSA-N 1,2-dimethoxypropane Chemical compound COCC(C)OC LEEANUDEDHYDTG-UHFFFAOYSA-N 0.000 description 1
- IDQBJILTOGBZCR-UHFFFAOYSA-N 1-butoxypropan-1-ol Chemical compound CCCCOC(O)CC IDQBJILTOGBZCR-UHFFFAOYSA-N 0.000 description 1
- JLBXCKSMESLGTJ-UHFFFAOYSA-N 1-ethoxypropan-1-ol Chemical compound CCOC(O)CC JLBXCKSMESLGTJ-UHFFFAOYSA-N 0.000 description 1
- LHENQXAPVKABON-UHFFFAOYSA-N 1-methoxypropan-1-ol Chemical compound CCC(O)OC LHENQXAPVKABON-UHFFFAOYSA-N 0.000 description 1
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
- JDSQBDGCMUXRBM-UHFFFAOYSA-N 2-[2-(2-butoxypropoxy)propoxy]propan-1-ol Chemical compound CCCCOC(C)COC(C)COC(C)CO JDSQBDGCMUXRBM-UHFFFAOYSA-N 0.000 description 1
- NQBXSWAWVZHKBZ-UHFFFAOYSA-N 2-butoxyethyl acetate Chemical compound CCCCOCCOC(C)=O NQBXSWAWVZHKBZ-UHFFFAOYSA-N 0.000 description 1
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
- VXKUOGVOWWPRNM-UHFFFAOYSA-N 3-ethoxypropyl acetate Chemical compound CCOCCCOC(C)=O VXKUOGVOWWPRNM-UHFFFAOYSA-N 0.000 description 1
- CCTFMNIEFHGTDU-UHFFFAOYSA-N 3-methoxypropyl acetate Chemical compound COCCCOC(C)=O CCTFMNIEFHGTDU-UHFFFAOYSA-N 0.000 description 1
- LDMRLRNXHLPZJN-UHFFFAOYSA-N 3-propoxypropan-1-ol Chemical compound CCCOCCCO LDMRLRNXHLPZJN-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000012080 ambient air Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229960002887 deanol Drugs 0.000 description 1
- 238000007791 dehumidification Methods 0.000 description 1
- 239000012972 dimethylethanolamine Substances 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 238000004070 electrodeposition Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 239000001034 iron oxide pigment Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011859 microparticle Substances 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 230000003287 optical effect Effects 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
- 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
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- RQGPLDBZHMVWCH-UHFFFAOYSA-N pyrrolo[3,2-b]pyrrole Chemical compound C1=NC2=CC=NC2=C1 RQGPLDBZHMVWCH-UHFFFAOYSA-N 0.000 description 1
- 230000003134 recirculating effect Effects 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000008096 xylene 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
- B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
-
- 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
- B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
- B05D7/50—Multilayers
- B05D7/52—Two layers
- B05D7/53—Base coat plus clear coat type
- B05D7/534—Base coat plus clear coat type the first layer being let to dry at least partially before applying the second layer
Definitions
- the invention relates to a method for producing two-layer Automotive top coats made of basecoat and clearcoat topcoat.
- One is e.g. known from GB-A-2 233 257.
- Two-coat automotive top coats are produced by wet-on-wet application a transparent top coat on one by flashing pre-dried color and / or effect basecoat.
- the non-aqueous basecoats contain organic Solvents in the order of, for example, from 55 to 80 wt .-%, while the aqueous basecoats only, for example, 10 to 25% by weight of organic solvents contain.
- the trend is therefore towards one Substitution of basecoats based on organic solvents by aqueous Basecoats. For example, older paint shops in which non-aqueous Basecoats are processed by new ones for processing Water-based paints designed painting systems replaced.
- the flash-off conditions for basecoat layers in painting systems for the application of basecoats based on organic solvents are different from those in Painting systems specially designed for the application of waterborne basecoats are.
- there are ventilation conditions which are marked due to short flash-off times of, for example, 30 to 180 seconds Air temperatures of, for example, 20 to 30 ° C.
- Air temperatures for example, 20 to 30 ° C.
- Waterborne basecoats take longer Flash-off times at higher air temperatures to result in the flash-off process complete the production of a pre-dried basecoat film.
- the flash-off times are therefore for example 5 to 10 minutes and the time during the drying Air temperatures are higher, for example at 40 to 80 ° C.
- the object of the invention is to provide a method for manufacturing two-coat automotive top coats by wet-on-wet application of one aqueous basecoat and a clearcoat under Granting of short flash-off times of, for example, 30 to 180 seconds for the Basecoat.
- the method should enable aqueous basecoats in to process automated automotive OEM painting systems for the Processing of non-aqueous basecoats are designed and only short flash-off times for allow the basecoat layers.
- the task can be solved by observing the following conditions the formulation of aqueous basecoat coatings and compliance with the following Process conditions during the flashing off of these aqueous Basecoat coating agents applied coating layers.
- the invention therefore relates to a method for producing a two-layer color and / or effect top coat Motor vehicle bodies in an automatic automotive painting system, wherein a transparent top coat layer from a clear lacquer coating agent onto one an aqueous color and / or effect basecoat and applied flashed-off basecoat and the two coating layers together branding, which is characterized in that an aqueous Basecoat coating agent used, which organic solvent accordingly contains a high solid value of 40 to 70%, and taking the basecoat film after their application and before application of the transparent top coat layer 30 to 180 Seconds with circulating air from 25 to 45 ° C with an air flow from 0.10 to 0.70 m / s, based on the surface provided with the aqueous basecoat film, vented.
- aqueous basecoat coating compositions are used.
- they each contain one or more conventional binders, organic Solvents and pigments and optionally fillers, crosslinkers and / or customary paint additives.
- the aqueous used in the process according to the invention Basecoat coatings for example, have weight solids contents of 15 to 50% by weight, for effect waterborne basecoats it is preferably 15 to 30, for example % By weight, for plain-colored water-based paints it is preferably higher, for example 20 to 45% by weight.
- the weight solids of the aqueous basecoat coating compositions is formed from the sum of the solid contributions of the binders, pigments, Fillers, crosslinkers and non-volatile additives common in paint.
- the Weight ratio of pigment to binder in the aqueous basecoat coating composition is, for example, between 0.05: 1 to 3: 1, for effect water-based paints it is for example preferably 0.1: 1 to 0.6: 1, for plain-colored water-based paints it is preferably higher, for example at 0.1: 1 to 2.5: 1, in each case based on the Solid weight.
- the ratio of pigment to binder is the sum of the parts by weight of coloring pigments, effect pigments and fillers related to the sum of the weight percentages of binder, Paste resin and crosslinker solids in the finished water-based paint.
- the aqueous basecoat coating compositions used in the process according to the invention have a high solid value of 40 to 70%.
- the high solid value of the aqueous basecoat coating compositions is calculated using the formula Solids content in% by weight x 100% Solids content in% by weight + content of organic solvents in% by weight.
- Solvent content and solids content must therefore be coordinated so that according to the above formula gives a high solid value of 40 to 70%.
- the waterborne basecoats used in the process according to the invention contain customary ones Binder systems stabilized ionically or non-ionically. These are preferred anionically and / or non-ionically stabilized. Anionic stabilization is preferred achieved by at least partially neutralized carboxyl groups in the binder, while non-ionic stabilization preferred by lateral or terminal Polyethylene oxide units in the binder is achieved.
- the water-based paints can be physically drying in nature or crosslinkable to form covalent bonds his. In the case of crosslinking with the formation of covalent bonds Waterborne basecoats can be self- or externally crosslinking systems. In the latter case, it can be one-component or multi-component water-based paints act.
- the waterborne basecoats used in the process according to the invention contain a or several common film-forming binders. You can if the binders don't are self-crosslinking or self-drying, optionally also contain crosslinking agents. Both the binder component and the crosslinker component which may be present is not subject to any limitation.
- film-forming binders for example Usual polyester, polyurethane and / or poly (meth) acrylate resins can be used.
- the selection of the crosslinking agents which may be present is not critical, it is directed in a manner familiar to the person skilled in the art according to the functionality of the binders.
- the waterborne basecoats used in the process according to the invention contain color and / or effect pigments and optionally fillers.
- coloring inorganic or organic pigments and fillers are titanium dioxide, micronized titanium dioxide, iron oxide pigments, carbon black, silicon dioxide, barium sulfate, micronized mica, talc, kaolin, chalk, layered silicates, azo pigments, Phthalocyanine pigments, quinacridone pigments, pyrrolopyrrole pigments, Perylene pigments.
- effect pigments are metal pigments, e.g. out Aluminum, copper or other metals; Interference pigments such as metal oxide coated metal pigments, e.g. titanium dioxide coated aluminum, coated mica such as titanium dioxide coated mica, Graphite effect pigments, platelet-shaped iron oxide, platelet-shaped Copper phthalocyanine pigments.
- Effect pigments are generally presented in the form of a commercially available aqueous or non-aqueous paste, optionally mixed with preferably water-dilutable organic solvents and additives and then mixed with an aqueous binder under scissors.
- Powdery effect pigments can first be processed into a paste with preferably water-dilutable organic solvents and additives.
- Color pigments and / or fillers can be rubbed, for example, in part of the aqueous binder. The rubbing can preferably also take place in a special water-thinnable paste resin. Grinding can be carried out in conventional units known to those skilled in the art. Then complete with the remaining portion of the aqueous binder or the aqueous paste resin for finished pigment pigment grinding.
- the waterborne basecoats used in the process according to the invention can contain further paint additives in conventional paint quantities, for example between 0.1 and 5% by weight, based on their solids content.
- further additives are neutralizing agents, anti-foaming agents, wetting agents, adhesion-promoting substances, catalysts, leveling agents, anti-cratering agents, light stabilizers and thickeners such as, for example, synthetic polymers with ionic and / or associative groups such as polyvinyl alcohol, poly (meth) acrylamide, poly (meth) acrylic acid , Polyvinylpyrrolidone, hydrophobically modified ethoxylated polyurethanes or polyacrylates, crosslinked or uncrosslinked polymer microparticles.
- the organic solvent in the waterborne basecoats preferably consists of 30 up to 60% by weight of low-boiling, for example preferably below 120 ° C. boiling, miscible with water or without a miscibility gap, for example one Water solubility at 20 ° C of more than 70 g per liter of water, organic solvents.
- Such organic ones are preferably selected Solvents from methanol, ethanol, n-propanol, isopropanol, n-butanol, 2-butanol, Isobutanol, methoxypropanol, methyl ethyl ketone, acetone or mixtures thereof; n- and isopropanol are particularly preferred.
- Water-based paints used in the process may be present, and preferably 40 to 70 Make up% by weight of the organic solvent composition in the waterborne basecoat are monohydric alcohols with 5 and more carbon atoms, e.g. Hexanol; Ethylene glycol ether or ester, e.g. Ethylene glycol dimethyl ether, Diethylene glycol mono- or di-C1-C6-alkyl ether, butyl glycol, butyl diglycol, Ethyl glycol acetate, butyl glycol acetate; Propylene glycol ether or ester, e.g.
- monohydric alcohols with 5 and more carbon atoms e.g. Hexanol
- Ethylene glycol ether or ester e.g. Ethylene glycol dimethyl ether, Diethylene glycol mono- or di-C1-C6-alkyl ether, butyl glycol, butyl diglycol, Ethyl glycol a
- the water-based paints are applied to motor vehicle bodies, which can consist of one type of substrate or of several types of substrates connected to one another in a mixed construction.
- it is metallic or plastic substrates.
- plastic substrates can be provided with a plastic primer, for example, metallic substrates generally have a primer applied, for example, electrophoretically and, if appropriate, additionally one or more further lacquer layers, such as a filler layer.
- the water-based varnishes are by spraying in one or more coats to a dry film thickness of 10 to 50 ⁇ m is applied, for effect water-based paints the dry film thickness is, for example, preferably 10 to 25 ⁇ m, for single-color aqueous base lacquers it is preferably higher, for example from 15 to 40 ⁇ m .
- Waterborne basecoat and clearcoat are applied in the invention Process according to the known wet-on-wet principle, i.e. those from the aqueous Basecoat coating agent applied basecoat is applied before the application of the The clear coat is first pre-dried by flashing off.
- the invention Pre-drying by ventilation is important so that the finished two-coat finish both the requirements on the technological properties such as Adhesion and stone chip resistance as well as to the optical properties such as For example, color, effect formation and top coat level met.
- aqueous basecoat coating agents used in the process according to the invention it is essential to the invention that one from the aqueous basecoat created basecoat layers after application and before application of the transparent Top coat layer 30 to 180 seconds with air circulation from 25 to 45 ° C with a Air flow rate from 0.10 to 0.70 m / s, based on that with the aqueous Basecoat provided surface, vented.
- the applied waterborne basecoat is flashed off in the Basecoat flash-off zone of automotive OEM painting and lasts 30 to 180 Seconds, preferably 60 to 150 seconds. This time period results, for example from the overall length of the basecoat flash-off zone of the automotive OEM painting system from for example 5 to 15 m and the belt speed of for example 2 to 6 m / min.
- the ventilation takes place under recirculating air conditions Air temperatures of 25 to 45 ° C, preferably 30 to 40 ° C.
- the ambient air conditions are chosen so that with a coated with an aqueous basecoat Surface air flow rate from 0.10 to 0.70 m / s, preferably 0.15 to 0.60 m / s is worked.
- the surface coated with an aqueous basecoat The air flow obtained is calculated as the quotient of the per second through the Exhaust zone the air volume in cubic meters and that in the exhaust zone existing surface coated with aqueous basecoat and to be vented, for example on the order of 20 to 150 square meters. That in Process according to the invention through the vented air volume is, for example, 1 to 2 cubic meters per running meter of ventilation zone and Second.
- the one in the flash-off zone is coated with an aqueous basecoat and surface to be ventilated is calculated from the number of in the basecoat flash-off zone coated motor vehicle bodies, e.g.
- the air is vented under circulating air conditions.
- the circulating air 5 to 15 g of water per cubic meter having.
- the fresh air contains preferably less than 15 g, particularly preferably 5 to 12 g of water per cubic meter.
- the adjustment of the water content of the admixed fresh air can be done by conventional means Dehumidification methods such as Compression of air and / or condensation or absorption of water from air.
- the circulating air is expediently at a flow rate of 4 to 8 m / s, measured on the object, moved. It is preferably a turbulent air flow from top to bottom and from the sides to the with of the body to be ventilated is provided.
- the air duct expediently takes place evenly and perpendicularly to the air to be vented Basecoat. The air is expediently extracted downwards.
- the flash-off zone can be under constant operating conditions or under variation single or multiple operating parameters can be operated.
- the variation of Operating parameters can take the form of a continuous or abrupt change over the entire length or one or more parts of the length of the Flash off zone.
- the venting zone can be in one or more, for example 1 to 3 zones can be divided, which can be separated from one another by locks.
- the variation of the operating parameters during the ventilation always lies within the limits set by the invention for the whole ventilating process.
- the venting zone in 2nd Zones is divided, with the bodies coated with water-based paint first in the first zone at low air temperatures, for example from 25 to 30 ° C, and then in the second zone at higher air temperatures, for example 30 ventilated up to 45 ° C;
- the air throughput can be, for example, in both Zones are selected to be the same height or different, for example in the first Zone lower than in the second, for example, the measured on the object Circulating air flow velocity in the second zone above 8 m / s lie.
- the average air flow rate however, within that of the invention predetermined limits.
- the pre-dried by flashing off the water base coat layers are overcoated with a conventional m chemically cross-linking clear coat in a dry layer thickness of, for example 30 to 100 ⁇ and baked together with the latter at temperatures of, for example 100 to 150 ° C.
- An advantage of the method according to the invention results from the low air temperatures that prevail during the ventilation of the water-based lacquer layers. It is thus possible for the flashed-off basecoat layers to be overpainted with a clear lacquer without the bodies having cooled down beforehand.
- all known clearcoats or transparent pigmented coating agents are suitable as clearcoats.
- Solvent-containing one-component (1K) or two-component (2K) clearcoats, water-dilutable 1K or 2K clearcoats, powder clearcoats or aqueous powder clearcoat slurries can be used.
- the stoving conditions of the two-coat system consisting of waterborne basecoat and clearcoat depend on the clearcoat system used.
- the method according to the invention allows the production of two layers Motor vehicle topcoats made from aqueous basecoat and clearcoat according to the wet-on-wet method with only short flash-off times from 30 to 180 seconds for the basecoat film. It is with the method according to the invention possible to apply waterborne basecoats in automated automotive painting systems are designed for the processing of non-aqueous basecoats and only short Allow flash-off times for the basecoat layers to be processed. An elaborate Conversion of such unsuitable for the processing of aqueous basecoats Painting systems can be avoided.
- the method according to the invention can even be carried out in this way be that both the Waterborne basecoats as well as non-aqueous basecoats can be processed.
- a car body is coated in a painting booth for experimental purposes:
- a cathodic electrodeposition primed and provided with a filler layer 4.3 m long car chassis is in a dry film thickness of 15 ⁇ m with a silver-colored water-based paint (composition: Solids content 20 wt .-%, dimethylethanolamine 1 wt .-%, butylglycol 8.5 % By weight, N-methylpyrrolidone 2% by weight, water 59% by weight, n-propanol 7% by weight, n-butanol 2.5% by weight, high solid value: 50%; Pigment / binder ratio: 0.2: 1) coated.
- the coated area is approximately 20 square meters.
- the mixture is then vented in a 5 m long ventilation zone with circulating air (water content 12 g per cubic meter) of 40 ° C for 90 s.
- the air circulation rate is 1.5 cubic meters per second and running meter of ventilation zone.
- venting is m painted and baked 30 minutes at 135 ° C (object temperature) with a commercial two-component clear coat in a dry film thickness of 35 ⁇ .
- the paint obtained is cooker-free and corresponds to the others technological requirements of modern automotive painting.
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Glass Compositions (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19906247A DE19906247A1 (de) | 1999-02-15 | 1999-02-15 | Verfahren zur Herstellung zweischichtiger Automobildecklackierungen |
| DE19906247 | 1999-02-15 | ||
| PCT/EP2000/001132 WO2000048748A1 (de) | 1999-02-15 | 2000-02-11 | Verfahren zur herstellung zweischichtiger automobildecklackierungen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP1112126A1 EP1112126A1 (de) | 2001-07-04 |
| EP1112126B1 true EP1112126B1 (de) | 2001-12-05 |
Family
ID=7897539
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP00907551A Expired - Lifetime EP1112126B1 (de) | 1999-02-15 | 2000-02-11 | Verfahren zur herstellung zweischichtiger automobildecklackierungen |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US6548119B1 (enExample) |
| EP (1) | EP1112126B1 (enExample) |
| JP (1) | JP2002537099A (enExample) |
| KR (1) | KR100603997B1 (enExample) |
| CN (1) | CN1156341C (enExample) |
| AT (1) | ATE209972T1 (enExample) |
| AU (1) | AU759783B2 (enExample) |
| BR (1) | BR0008215B1 (enExample) |
| CZ (1) | CZ299010B6 (enExample) |
| DE (2) | DE19906247A1 (enExample) |
| ES (1) | ES2170048T3 (enExample) |
| MX (1) | MXPA01008258A (enExample) |
| WO (1) | WO2000048748A1 (enExample) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10043405C1 (de) * | 2000-09-04 | 2002-06-27 | Basf Coatings Ag | Verfahren zur Herstellung farb- und/oder effektgebender Lackierungen |
| DE10045608A1 (de) * | 2000-09-15 | 2002-03-28 | Volkswagen Ag | Verfahren und Vorrichtung zum Trocknen einer lackierten Kraftfahrzeugkarosserie |
| WO2003039767A1 (fr) * | 2001-11-05 | 2003-05-15 | Kansai Paint Co., Ltd. | Procede de formation de film a revetement multicouches |
| US20060035692A1 (en) * | 2002-02-08 | 2006-02-16 | Keith Kirby | Collectible item and code for interactive games |
| TW200530352A (en) * | 2004-02-09 | 2005-09-16 | Nippon Paint Co Ltd | Metallic base coating composition and process for producing a composite film |
| US20050250416A1 (en) * | 2004-04-23 | 2005-11-10 | Barthold Mark J | Toy and card package |
| US20050250415A1 (en) * | 2004-04-23 | 2005-11-10 | Barthold Mark J | Toy and card package |
| US7166331B2 (en) * | 2004-05-10 | 2007-01-23 | E. I. Du Pont De Nemours And Company | Process for the production of multi-layer coatings comprising a waterborne primer-surfacer layer and a topcoat applied thereto |
| US20060079149A1 (en) * | 2004-10-08 | 2006-04-13 | Nathan Proch | Cut-out logo display |
| US20060076735A1 (en) * | 2004-10-08 | 2006-04-13 | Nathan Proch | Wheel having a translucent aspect |
| US20060079150A1 (en) * | 2004-10-08 | 2006-04-13 | Miva Filoseta | Toy for collecting and dispersing toy vehicles |
| US20060078684A1 (en) * | 2004-10-08 | 2006-04-13 | Neo Tian B | Paint process for toys |
| DE102005001683B4 (de) * | 2005-01-13 | 2010-01-14 | Venjakob Maschinenbau Gmbh & Co. Kg | Verfahren und Vorrichtung zum Trocknen von Lackschichten |
| EP2394746A1 (de) | 2010-06-14 | 2011-12-14 | Saint-Gobain Glass France | Verfahren zur Flutbeschichtung eines polymeren Werkstoffes |
| EP2394747A1 (de) | 2010-06-14 | 2011-12-14 | Saint-Gobain Glass France | Verfahren zur Flutbeschichtung eines polymeren Werkstoffes |
| US20230347380A1 (en) * | 2020-09-15 | 2023-11-02 | Axalta Coating Systems Ip Co., Llc | Methods for coating substrates |
| CN116809350A (zh) * | 2022-03-22 | 2023-09-29 | 本田技研工业株式会社 | 涂装方法及涂装系统 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3210051A1 (de) * | 1982-03-19 | 1983-09-29 | Basf Farben + Fasern Ag, 2000 Hamburg | Wasserverduennbares ueberzugsmittel zur herstellung der basisschicht eines mehrschichtueberzuges |
| JPH02144179A (ja) * | 1988-11-22 | 1990-06-01 | Bou Kojima | 被塗装物へのポリテトラフルオロエチレン系塗料のコーティング方法 |
| CA2012161C (en) | 1989-06-12 | 1999-03-16 | Yoshio Tomioka | Apparatus for painting |
| US5168105A (en) * | 1990-09-10 | 1992-12-01 | Basf Corporation | Metallic water borne base coat composition based on acrylic latex resins using an acrylic resin having acid and nonionic functionality for aluminum storage and a treated hetorite clay for rheology control-water base 5 |
| US5236995A (en) * | 1991-03-26 | 1993-08-17 | Basf Corporation | Post-extended anionic polyurethane dispersion |
| DE19517277C2 (de) * | 1995-05-11 | 2000-11-09 | Herberts Gmbh | Verfahren zur Herstellung von Mehrschicht-Effektlackierungen |
| DE19717520C1 (de) | 1997-04-25 | 1999-03-04 | Basf Coatings Ag | Verfahren zur Herstellung einer mehrschichtigen Lackierung |
| US6035547A (en) * | 1998-08-17 | 2000-03-14 | Chrysler Corporation | Water-borne basecoat flash process |
-
1999
- 1999-02-15 DE DE19906247A patent/DE19906247A1/de not_active Withdrawn
-
2000
- 2000-02-11 ES ES00907551T patent/ES2170048T3/es not_active Expired - Lifetime
- 2000-02-11 AT AT00907551T patent/ATE209972T1/de not_active IP Right Cessation
- 2000-02-11 CZ CZ20012941A patent/CZ299010B6/cs not_active IP Right Cessation
- 2000-02-11 WO PCT/EP2000/001132 patent/WO2000048748A1/de not_active Ceased
- 2000-02-11 AU AU29104/00A patent/AU759783B2/en not_active Ceased
- 2000-02-11 KR KR1020017010332A patent/KR100603997B1/ko not_active Expired - Fee Related
- 2000-02-11 CN CNB008038066A patent/CN1156341C/zh not_active Expired - Fee Related
- 2000-02-11 JP JP2000599520A patent/JP2002537099A/ja active Pending
- 2000-02-11 EP EP00907551A patent/EP1112126B1/de not_active Expired - Lifetime
- 2000-02-11 BR BRPI0008215-5A patent/BR0008215B1/pt not_active IP Right Cessation
- 2000-02-11 MX MXPA01008258A patent/MXPA01008258A/es active IP Right Grant
- 2000-02-11 US US09/913,568 patent/US6548119B1/en not_active Expired - Fee Related
- 2000-02-11 DE DE50000049T patent/DE50000049D1/de not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| KR20010102145A (ko) | 2001-11-15 |
| CZ20012941A3 (cs) | 2002-03-13 |
| CN1156341C (zh) | 2004-07-07 |
| DE50000049D1 (de) | 2002-01-17 |
| WO2000048748A1 (de) | 2000-08-24 |
| MX229728B (enExample) | 2005-08-05 |
| BR0008215A (pt) | 2001-10-30 |
| KR100603997B1 (ko) | 2006-07-25 |
| CN1339989A (zh) | 2002-03-13 |
| BR0008215B1 (pt) | 2011-03-22 |
| MXPA01008258A (es) | 2002-10-23 |
| JP2002537099A (ja) | 2002-11-05 |
| DE19906247A1 (de) | 2000-08-17 |
| AU759783B2 (en) | 2003-05-01 |
| AU2910400A (en) | 2000-09-04 |
| ES2170048T3 (es) | 2002-08-01 |
| ATE209972T1 (de) | 2001-12-15 |
| US6548119B1 (en) | 2003-04-15 |
| CZ299010B6 (cs) | 2008-04-02 |
| EP1112126A1 (de) | 2001-07-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP1112126B1 (de) | Verfahren zur herstellung zweischichtiger automobildecklackierungen | |
| DE19512017C1 (de) | Verfahren zur Mehrschichtlackierung | |
| DE19606716C1 (de) | Verfahren zur Mehrschichtlackierung | |
| DE60018598T2 (de) | Verfahren und vorrichtung zur beschichtung eines substrates | |
| EP0904160B1 (de) | Verfahren zur herstellung von mehrschichtlackierungen auf elektrisch leitfähigen substraten | |
| EP0902731B1 (de) | Verfahren zur herstellung von mehrschichtigen überzügen | |
| DE4308859A1 (de) | Füllstoffpaste zur Verwendung in Basislacken zur Beschichtung von Polyolefin-Substraten, Basislacke sowie Verfahren zur Direktlackierung von Polyolefin-Substraten | |
| DE4437841A1 (de) | Füllstoffkomponente zur Verwendung in wäßrigen Basislacken | |
| DE19519665C1 (de) | Verfahren zur Mehrschichtlackierung | |
| EP0698069B1 (de) | Füllstoffpaste zur verwendung in basislacken zur beschichtung von kunststoff- und metallsubstraten, basislacke sowie verfahren zur direktlackierung von metall- und kunststoffsubstraten | |
| DE19529394C2 (de) | Verfahren zur Herstellung von Mehrschichtlackierungen auf Metallsubstraten | |
| WO1995007148A1 (de) | Verfahren zur herstellung einer mehrschichtigen reparaturlackierung | |
| DE602005005628T2 (de) | Verfahren zur herstellung von zweifarbig überzogenen substraten | |
| EP0764475B1 (de) | Verfahren zur Effektlackierung genarbter Kunststoffteile | |
| EP1040875B1 (de) | Softfeeling-Mehrschichtlackierung | |
| DE60110492T2 (de) | Verfahren zur Reparaturbeschichtung von Mehrschichtüberzügen auf Substraten | |
| WO1998023390A1 (de) | Verfahren zur mehrschichtlackierung | |
| EP1124907B1 (de) | Zweischichtlackierung aus wässrigem basislack und klarlack mit verbesserter klarlackbenetzungsgrenze | |
| DE4422287A1 (de) | Verfahren zur Herstellung von Effektlackierungen | |
| EP0915116B1 (de) | Verfahren zur Herstellung von Mehrschichtlackierungen | |
| DE19754182C2 (de) | Wäßrige Schichtsilikatdispersionen und deren Verwendung bei der Herstellung rheologieoptimierter wäßriger Überzugsmittel | |
| DE19628361A1 (de) | Verfahren zur Herstellung von Mehrschichtlackierungen auf elektrisch leitfähigen Substraten | |
| DE102011115342A1 (de) | Verfahren zur Herstellung einer Mattlackierung auf einer Substratoberfläche | |
| DE19851576A1 (de) | Wäßrige Basislacke und ihre Verwendung zur Mehrschichtlackierung | |
| JPH0833865A (ja) | ウエットオンウエット塗装方法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
| 17P | Request for examination filed |
Effective date: 20001204 |
|
| AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE |
|
| GRAG | Despatch of communication of intention to grant |
Free format text: ORIGINAL CODE: EPIDOS AGRA |
|
| 17Q | First examination report despatched |
Effective date: 20010719 |
|
| GRAG | Despatch of communication of intention to grant |
Free format text: ORIGINAL CODE: EPIDOS AGRA |
|
| GRAH | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOS IGRA |
|
| GRAH | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOS IGRA |
|
| GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
| AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20011205 Ref country code: FI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20011205 Ref country code: GR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20011205 Ref country code: IE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20011205 |
|
| REF | Corresponds to: |
Ref document number: 209972 Country of ref document: AT Date of ref document: 20011215 Kind code of ref document: T |
|
| REG | Reference to a national code |
Ref country code: CH Ref legal event code: EP |
|
| REG | Reference to a national code |
Ref country code: GB Ref legal event code: IF02 |
|
| GBT | Gb: translation of ep patent filed (gb section 77(6)(a)/1977) |
Effective date: 20011206 |
|
| REG | Reference to a national code |
Ref country code: IE Ref legal event code: FG4D Free format text: GERMAN |
|
| REF | Corresponds to: |
Ref document number: 50000049 Country of ref document: DE Date of ref document: 20020117 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LU Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20020211 Ref country code: AT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20020211 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: CY Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20020228 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: PT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20020305 Ref country code: DK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20020305 |
|
| ET | Fr: translation filed | ||
| NLV1 | Nl: lapsed or annulled due to failure to fulfill the requirements of art. 29p and 29m of the patents act | ||
| REG | Reference to a national code |
Ref country code: IE Ref legal event code: FD4D |
|
| REG | Reference to a national code |
Ref country code: ES Ref legal event code: FG2A Ref document number: 2170048 Country of ref document: ES Kind code of ref document: T3 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MC Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20020901 |
|
| PLBQ | Unpublished change to opponent data |
Free format text: ORIGINAL CODE: EPIDOS OPPO |
|
| PLBI | Opposition filed |
Free format text: ORIGINAL CODE: 0009260 |
|
| PLBF | Reply of patent proprietor to notice(s) of opposition |
Free format text: ORIGINAL CODE: EPIDOS OBSO |
|
| 26 | Opposition filed |
Opponent name: BASF COATINGS AG Effective date: 20020830 |
|
| PLBF | Reply of patent proprietor to notice(s) of opposition |
Free format text: ORIGINAL CODE: EPIDOS OBSO |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LI Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20040229 Ref country code: CH Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20040229 |
|
| PLCK | Communication despatched that opposition was rejected |
Free format text: ORIGINAL CODE: EPIDOSNREJ1 |
|
| PLBN | Opposition rejected |
Free format text: ORIGINAL CODE: 0009273 |
|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: OPPOSITION REJECTED |
|
| 27O | Opposition rejected |
Effective date: 20040422 |
|
| REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: ES Payment date: 20090317 Year of fee payment: 10 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20090211 Year of fee payment: 10 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: BE Payment date: 20090216 Year of fee payment: 10 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: IT Payment date: 20090213 Year of fee payment: 10 Ref country code: SE Payment date: 20090206 Year of fee payment: 10 |
|
| BERE | Be: lapsed |
Owner name: E.I. *DU PONT DE NEMOURS & CY INC. Effective date: 20100228 |
|
| EUG | Se: european patent has lapsed | ||
| GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20100211 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: BE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20100228 |
|
| REG | Reference to a national code |
Ref country code: ES Ref legal event code: FD2A Effective date: 20110330 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20100211 Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20100211 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20110208 Year of fee payment: 12 Ref country code: FR Payment date: 20110218 Year of fee payment: 12 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: ES Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20110317 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: ES Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20100212 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20100212 |
|
| REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST Effective date: 20121031 |
|
| REG | Reference to a national code |
Ref country code: DE Ref legal event code: R119 Ref document number: 50000049 Country of ref document: DE Effective date: 20120901 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20120229 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20120901 |