WO2000015722A1 - Zweischichtlackierung aus wässrigem basislack und klarlack mit verbesserter klarlackbenetzungsgrenze - Google Patents
Zweischichtlackierung aus wässrigem basislack und klarlack mit verbesserter klarlackbenetzungsgrenze Download PDFInfo
- Publication number
- WO2000015722A1 WO2000015722A1 PCT/EP1999/006441 EP9906441W WO0015722A1 WO 2000015722 A1 WO2000015722 A1 WO 2000015722A1 EP 9906441 W EP9906441 W EP 9906441W WO 0015722 A1 WO0015722 A1 WO 0015722A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- varnish
- polyethylene
- oxide
- homopolymers
- copolymers
- Prior art date
Links
- 238000009736 wetting Methods 0.000 title claims abstract description 12
- 239000002966 varnish Substances 0.000 title abstract description 9
- 229920001519 homopolymer Polymers 0.000 claims abstract description 22
- -1 polyethylene Polymers 0.000 claims abstract description 22
- 239000004698 Polyethylene Substances 0.000 claims abstract description 20
- 229920000573 polyethylene Polymers 0.000 claims abstract description 20
- 229920001577 copolymer Polymers 0.000 claims abstract description 17
- 229920001451 polypropylene glycol Polymers 0.000 claims abstract description 17
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims abstract description 12
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims abstract description 7
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000000049 pigment Substances 0.000 claims description 24
- 239000011230 binding agent Substances 0.000 claims description 20
- 239000003973 paint Substances 0.000 claims description 17
- 238000000576 coating method Methods 0.000 claims description 14
- 239000011248 coating agent Substances 0.000 claims description 13
- 239000007787 solid Substances 0.000 claims description 13
- 239000004922 lacquer Substances 0.000 claims description 12
- 239000000654 additive Substances 0.000 claims description 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
- 239000000945 filler Substances 0.000 claims description 8
- 239000000758 substrate Substances 0.000 claims description 8
- 239000003431 cross linking reagent Substances 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 4
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical group C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 claims 1
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical class CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 16
- 230000000694 effects Effects 0.000 description 12
- 238000004519 manufacturing process Methods 0.000 description 12
- 235000013772 propylene glycol Nutrition 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 229920005862 polyol Polymers 0.000 description 11
- 150000003077 polyols Chemical class 0.000 description 10
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical class OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 7
- 238000010422 painting Methods 0.000 description 7
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 5
- 239000004924 water-based lacquer Substances 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 239000004814 polyurethane Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 239000002904 solvent Substances 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
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- 239000004971 Cross linker Substances 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-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
- 238000004040 coloring Methods 0.000 description 3
- 230000000295 complement effect Effects 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000010348 incorporation 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
- 229920000728 polyester Polymers 0.000 description 3
- 229920002635 polyurethane Polymers 0.000 description 3
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 3
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-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
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 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
- ARZLUCYKIWYSHR-UHFFFAOYSA-N hydroxymethoxymethanol Chemical compound OCOCO ARZLUCYKIWYSHR-UHFFFAOYSA-N 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000006259 organic additive Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- JLBXCKSMESLGTJ-UHFFFAOYSA-N 1-ethoxypropan-1-ol Chemical compound CCOC(O)CC JLBXCKSMESLGTJ-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 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
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-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
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 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
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 229920003180 amino resin Polymers 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
- 239000011324 bead Substances 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 235000019646 color tone Nutrition 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 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
- 239000012972 dimethylethanolamine Substances 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 150000002334 glycols Chemical class 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
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-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
- 239000000463 material 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
- 239000012860 organic pigment Substances 0.000 description 1
- 150000002924 oxiranes Chemical class 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-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
- 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
- 229920000570 polyether Polymers 0.000 description 1
- 229920001223 polyethylene glycol 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
- 238000002360 preparation method Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 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
- 239000001054 red pigment Substances 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
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 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
- 239000013638 trimer Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/02—Emulsion paints including aerosols
- C09D5/024—Emulsion paints including aerosols characterised by the additives
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
- Y10T428/31605—Next to free metal
Definitions
- the invention relates to the production of two-coat coatings of the basecoat / clearcoat type with an improved clearcoat wetting limit using certain additives in aqueous basecoats, and to aqueous basecoats suitable for this purpose. It also relates to a process for producing the
- EP-A-0 281 936 discloses waterborne basecoats which contain layered silicate dispersions prepared using polypropylene oxide as a protective colloid.
- the polypropylene oxides can contain ethylene oxide units in a randomly distributed form or in the form of a block copolymer structure.
- the block copolymeric polypropylene oxides those with an average molecular weight of 500 to 8000 are suitable.
- polypropylene oxide homopolymers with an average molecular weight of 400 to 1000, very particularly preferably about 900.
- decorative two-coat topcoats are increasingly being produced by applying a color and / or effect basecoat consisting of an aqueous basecoat and a protective clearcoat.
- the clear coat must be applied in a minimum layer thickness specified by the clear coat wetting limit in order to ensure the formation of a closed clear coat film on the entire substrate surface. In practice, this minimum layer thickness is even exceeded, for example in order to ensure the formation of a closed clear lacquer film at locations on the substrate that are difficult to reach by the application devices, such as beads, edges or depressions in an automobile body.
- the object of the invention is to provide waterborne basecoats for the subsequent overcoating with clearcoat layers, which likewise make it possible to lower the clearcoat wetting limits and to apply the clearcoat layer in question with the lowest possible layer thickness and to increase the process reliability in the clearcoat coating.
- the water-based paints should be easy and stable to produce.
- this object can be achieved by using one or more polyethylene and / or propylene glycols and / or polyols with an average molecular weight of more than 1000 to 8000 which are partially or completely etherified with C1-C4-alkanols as additives in waterborne basecoats.
- the invention therefore relates to the use of linear and / or branched polyethylene oxide homopolymers, polypropylene oxide homopolymers and / or polyethylene / propylene oxide copolymers with randomly distributed ethylene oxide and propylene oxide units, the terminal hydroxyl groups of the homo- or copolymers being unetherified or partially or completely with C1-C4-
- Alkanols can be etherified, with an average molecular mass of over 1000 to 8000 to reduce the clear lacquer wetting limit in the two-coat coating with aqueous basecoat and clearcoat.
- the average molecular weights mentioned are to be understood here as the calculated average molecular weights.
- the linear and / or branched polyethylene oxide homopolymers, polypropylene oxide homopolymers and / or polyethylene / propylene oxide copolymers added to the aqueous basecoat before its application, preferably in a proportion of 0.5 to 15% by weight, based on its solids content.
- Another object of the invention is an aqueous basecoat composition, each containing one or more binders and pigments and optionally fillers, crosslinking agents, organic solvents and / or customary paint additives, which is characterized in that it additionally contains one or more linear and / or branched polyethylene oxide homopolymers,
- the colored and / or effect water-based lacquers modified according to the invention can be used in the production of multi-layer lacquers, in particular decorative basecoat / clear lacquer two-layer lacquers.
- the waterborne basecoats contain ionic or non-ionically stabilized binder systems in a suitable manner. These are preferably anionically and / or non-ionically stabilized. Anionic stabilization is preferably achieved by at least partially neutralized carboxyl groups in the binder, while non-ionic stabilization is preferably achieved by lateral or terminal polyethylene oxide units in the binder.
- the water-based paints can be physically drying in nature or can be crosslinked to form covalent bonds.
- the aqueous basecoats which crosslink with the formation of covalent bonds can be self- or externally crosslinking systems. In the latter case, it can be a one- or multi-component waterborne basecoat.
- the waterborne basecoats according to the invention contain one or more customary ones film-forming binders. If the binders are not self-crosslinking or self-drying, they can optionally also contain crosslinking agents. Both the binder component and the crosslinker component which may be present are not subject to any restrictions. For example, conventional polyester, polyurethane and / or poly (meth) acrylate resins can be used as film-forming binders.
- crosslinking agents which may be present is not critical, it is based in the manner familiar to the person skilled in the art on the functionality of the binders, that is to say the crosslinking agents are selected such that they have a reactive functionality which is complementary to the functionality of the binder.
- Examples of such complementary functionalities between binder and crosslinker are: carboxyl / epoxide, hydroxyl / methylol ether and / or methylol (methylol ether and or methylol preferably as crosslinking groups of amino resins), hydroxyl / free isocyanate, hydroxyl / blocked isocyanate, (meth) acryloyl / CH-acidic group.
- complementary functionalities can also be present side by side in a water-based lacquer. The possibly in the
- Crosslinking agents contained in waterborne basecoats can be present individually or in a mixture.
- the waterborne basecoat materials according to the invention contain coloring and / or effect pigments and, if appropriate, fillers.
- coloring inorganic or organic pigments and fillers are titanium dioxide, microsized 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. made of aluminum, copper or other metals; Interference pigments such as metal oxide coated
- Metal pigments for example titanium dioxide-coated aluminum, coated mica such as, for example, titanium dioxide-coated mica, graphite effect pigments, platelet-shaped iron oxide, platelet-shaped copper phthalocyanine pigments.
- the effect pigments are generally introduced 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 are first 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 contain the polyethylene oxide homo-, polypropylene oxide homo- and / or polyethylene oxide / propylene oxide copolymers defined above.
- These can also be referred to as polyethylene glycols, polypropylene glycols, polyethylene / propylene glycols, which are partially or completely etherified with C1-C4-alkanols, or as corresponding polyols, provided that the latter are branched products.
- the expression "polyethylene and / or propylene glycols and / or polyols” is chosen for simplification.
- polyethylene oxide homopolymers or polypropylene oxide homopolymers or polyethylene / propylene oxide copolymers with randomly distributed ethylene oxide and propylene oxide units it being possible for the terminal hydroxyl groups of the homo- or copolymers to be etherified or partially or completely etherified with C 1 -C 4 -alkanols .
- the average molecular masses of the homopolymers or copolymers are preferably above 1000 to 4000, in particular around 2000.
- They can be branched polyethylene and / or propylene polyols which can be prepared by ring-opening polymerization of ethylene and / or propylene oxide using trifunctional or higher functional polyols as starter molecules, such as trimethylolpropane, glycerin, pentaerythritol.
- Linear polyethylene and / or propylene glycols are preferred in the context of the invention. These can be produced by ring-opening polymerization of ethylene oxide and / or propylene oxide
- water or diols as starter molecules, such as preferably ethylene glycol or propylene glycol.
- the homopolymeric representatives used as additives in the waterborne basecoats in particular the polypropylene oxide homopolymers.
- the terminal hydroxyl groups of the polyethylene and / or propylene glycols and / or polyols can be partially or completely etherified with C1-C4-alkanols, such as methanol, ethanol, n-propanol, isopropanol, 1-butanol, 2-butanol, isobutanol, however, the unetherified hydroxy-functional polyether compounds are preferred.
- the polyethylene and / or propylene glycols and / or polyols are used in a proportion of 0.5 to 15% by weight, preferably 1 to 10% by weight, based on the solids content of the waterborne basecoats.
- the incorporation of the polyethylene and / or propylene glycols and / or polyols can be carried out at any stage in the production of the waterborne basecoats, for example only as an additive to the waterborne basecoat itself, for example as a subsequently added correction agent.
- a stable incorporation of the polyethylene and / or propylene glycols and / or polyols is achieved without any special effort during the mixing process.
- the waterborne basecoats according to the invention can contain other customary paint additives in conventional paint quantities, for example between 0.1 and 5% by weight, based on their
- anti-foaming agents such as, for example, synthetic polymers with ionic and / or associative groups such as polyvinyl alcohol, poly (meth) acrylamide, poly (meth) acrylic acid, polyvinyl pyrrolidone , hydrophobically modified ethoxylated polyurethanes or polyacrylates, cross-linked or uncross-linked polymer microparticles.
- the waterborne basecoats according to the invention can contain customary paint solvents, for example in a proportion of preferably less than 20% by weight, particularly preferably less than 15% by weight. These are customary paint solvents, for example they can come from or become from the manufacture of the binders added separately.
- solvents examples include monohydric or polyhydric alcohols, for example propanol, butanol, hexanol; Glycol ethers or esters, for example diethylene glycol di-C 1 -C 6 alkyl ether, dipropylene glycol di C 1 -C 6 alkyl ether, ethoxypropanol, butyl glycol; Glycols, for example ethylene glycol and / or propylene glycol, and their di- or trimers, N-alkylpyrrolidones, such as, for example, N-methylpyrrohdon and
- Ketones such as methyl ethyl ketone, acetone, cyclohexanone; aromatic or aliphatic hydrocarbons, e.g. Toluene, xylene or linear or branched aliphatic C6 - C12-carbons hydrogen e.
- the waterborne basecoats of the invention have, for example, solids contents of 10 to 50% by weight, for effect waterborne basecoats it is preferably 15 to 30% by weight, for single-color waterborne basecoats it is preferably higher, for example 20 to 45% by weight.
- the weight ratio of pigment to binder in the waterborne basecoat is, for example, between 0.05: 1 to 3: 1, for effect waterborne basecoats it is preferably 0.1: 1 to 0.6: 1, for single-color waterborne basecoats, it is preferably higher, for example 0, 1: 1 to 2.5: 1, each based on the solid weight.
- the sum of the parts by weight of color pigments, effect pigments and fillers is related to the sum of the parts by weight of solid binder, solid paste resin and solid
- aqueous basecoats according to the invention are suitable for the production of multi-layer coatings, in particular color and / or effect-giving two-layer coatings in the motor vehicle sector. They are suitable for that
- Vehicle painting and refinishing can also be used in other areas, e.g. plastic painting, especially vehicle parts painting.
- the invention therefore also relates to a method for producing
- the waterborne basecoats according to the invention can be based on Various types of substrates can be applied. In general, it is metallic or plastic substrates. These are often precoated, ie plastic substrates can be provided, for example, with a plastic primer, metallic substrates generally have, for example, an electrophoretically applied primer and, if appropriate, additionally one or more others
- the waterborne basecoats according to the invention are preferably applied by spraying in a dry layer thickness of 8 to 50 ⁇ m, for effect waterborne basecoats the dry layer thickness is, for example, preferably 10 to 25 ⁇ m, for monochrome waterborne basecoats it is preferably higher, for example 10 to 40 ⁇ m.
- Application is preferably carried out wet-in
- the water-based lacquer layers are overpainted with a conventional clear lacquer in a dry layer thickness of preferably 30 to 60 ⁇ m and dried or crosslinked together with this at temperatures of, for example, 20 to 150 ° C.
- the drying conditions of the two-coat system consisting of waterborne basecoat and clearcoat depend on the clearcoat system used. For repair purposes, for example, temperatures of 20 to 80 ° C are preferred. Temperatures above 100 ° C., for example above 110 ° C., are preferred for the purposes of series painting.
- the formation of a puff-like, milky coating on the clear lacquer surface sometimes observed in the prior art, cannot be observed even in the case of dark colors when using the water-based lacquers according to the invention.
- One-component (1K) or two-component (2K) clearcoats are used.
- Two-component polyurethane clearcoats are preferably used for overcoating of basecoat layers prepared from waterborne basecoats according to the invention.
- Color tones that have low hiding power can be important, or in the case of water-based paints with an increased tendency to run off, for example highly pigmented water-based paints.
- Clear coat of a commercial two-component PU clear coat in one maximum dry layer thickness of 50 ⁇ m overcoated by spray application (wedge in the longitudinal direction of the test plate). After 5 rnin. Flash off at room temperature is baked for 30 minutes at 130 ° C (object temperature). The test plate was in a vertical position in the longitudinal direction.
- the visually perceptible clear lacquer wetting limit is 23 ⁇ m.
- Example lb is repeated with the uni-red waterborne basecoat from example 2a).
- the visually perceptible clear lacquer wetting limit is 13 ⁇ m.
Landscapes
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE59911155T DE59911155D1 (de) | 1998-09-14 | 1999-09-02 | Zweischichtlackierung aus wässrigem basislack und klarlack mit verbesserter klarlackbenetzungsgrenze |
EP99944583A EP1124907B1 (de) | 1998-09-14 | 1999-09-02 | Zweischichtlackierung aus wässrigem basislack und klarlack mit verbesserter klarlackbenetzungsgrenze |
AT99944583T ATE283321T1 (de) | 1998-09-14 | 1999-09-02 | Zweischichtlackierung aus wässrigem basislack und klarlack mit verbesserter klarlackbenetzungsgrenze |
US09/786,505 US6565979B1 (en) | 1998-09-14 | 1999-09-02 | Double-layer varnish comprising an aqueous base varnish and clear varnish with improved clear varnish wetting limit |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19841976A DE19841976A1 (de) | 1998-09-14 | 1998-09-14 | Zweischichtlackierung aus wäßrigem Basislack und Klarlack mit verbesserter Klarlackbenetzungsgrenze |
DE19841976.7 | 1998-09-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2000015722A1 true WO2000015722A1 (de) | 2000-03-23 |
Family
ID=7880882
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP1999/006441 WO2000015722A1 (de) | 1998-09-14 | 1999-09-02 | Zweischichtlackierung aus wässrigem basislack und klarlack mit verbesserter klarlackbenetzungsgrenze |
Country Status (6)
Country | Link |
---|---|
US (1) | US6565979B1 (de) |
EP (1) | EP1124907B1 (de) |
AT (1) | ATE283321T1 (de) |
DE (2) | DE19841976A1 (de) |
ES (1) | ES2228097T3 (de) |
WO (1) | WO2000015722A1 (de) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6669930B1 (en) * | 2003-01-15 | 2003-12-30 | Colgate Palmolive Company | Liquid tooth whitening gel |
JP2009543909A (ja) * | 2006-07-20 | 2009-12-10 | ビーエーエスエフ ソシエタス・ヨーロピア | 高官能性、高分岐または超分岐ポリカーボネートを含む水性塗料 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1451986A (en) * | 1973-02-20 | 1976-10-06 | Rohm & Haas | Coating compositions |
DE3120286A1 (de) * | 1980-06-07 | 1982-04-01 | Kansai Paint Co., Ltd., Amagasaki, Hyogo | "wasser-aufschlaemmungs-ueberzugs-zusammensetzung auf basis eines waermehaertbaren pulverharzes" |
EP0281936A1 (de) * | 1987-03-07 | 1988-09-14 | BASF Lacke + Farben AG | Wässrige Schichtsilikatdispersionen, Verwendung dieser Dispersionen als Lackhilfsmittel und wasserverdünnbare, Schichtsilikate enthaltende Beschichtungszusammensetzungen |
WO1994004616A1 (en) * | 1992-08-13 | 1994-03-03 | Courtaulds Coatings (Holdings) Limited | Segregating water-borne coating systems |
JPH0711185A (ja) * | 1993-06-24 | 1995-01-13 | Toyo Ink Mfg Co Ltd | 水性塗料組成物 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3807234A1 (de) * | 1988-03-05 | 1989-09-14 | Basf Ag | Waessrige anstrichstoffe |
DE4400854C2 (de) | 1994-01-14 | 1996-05-30 | Herberts Gmbh | Verwendung von Polybutenen zur Verbesserung der Verlaufsfähigkeit von Überzugsmitteln |
DE19532294A1 (de) * | 1995-09-01 | 1997-03-06 | Huels Chemische Werke Ag | Flüssige Einkomponenten-PUR-Einbrennlacke |
-
1998
- 1998-09-14 DE DE19841976A patent/DE19841976A1/de not_active Withdrawn
-
1999
- 1999-09-02 EP EP99944583A patent/EP1124907B1/de not_active Revoked
- 1999-09-02 ES ES99944583T patent/ES2228097T3/es not_active Expired - Lifetime
- 1999-09-02 WO PCT/EP1999/006441 patent/WO2000015722A1/de active IP Right Grant
- 1999-09-02 AT AT99944583T patent/ATE283321T1/de not_active IP Right Cessation
- 1999-09-02 US US09/786,505 patent/US6565979B1/en not_active Expired - Fee Related
- 1999-09-02 DE DE59911155T patent/DE59911155D1/de not_active Revoked
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1451986A (en) * | 1973-02-20 | 1976-10-06 | Rohm & Haas | Coating compositions |
DE3120286A1 (de) * | 1980-06-07 | 1982-04-01 | Kansai Paint Co., Ltd., Amagasaki, Hyogo | "wasser-aufschlaemmungs-ueberzugs-zusammensetzung auf basis eines waermehaertbaren pulverharzes" |
EP0281936A1 (de) * | 1987-03-07 | 1988-09-14 | BASF Lacke + Farben AG | Wässrige Schichtsilikatdispersionen, Verwendung dieser Dispersionen als Lackhilfsmittel und wasserverdünnbare, Schichtsilikate enthaltende Beschichtungszusammensetzungen |
WO1994004616A1 (en) * | 1992-08-13 | 1994-03-03 | Courtaulds Coatings (Holdings) Limited | Segregating water-borne coating systems |
JPH0711185A (ja) * | 1993-06-24 | 1995-01-13 | Toyo Ink Mfg Co Ltd | 水性塗料組成物 |
Non-Patent Citations (1)
Title |
---|
PATENT ABSTRACTS OF JAPAN vol. 1995, no. 04 31 May 1995 (1995-05-31) * |
Also Published As
Publication number | Publication date |
---|---|
DE59911155D1 (de) | 2004-12-30 |
ES2228097T3 (es) | 2005-04-01 |
DE19841976A1 (de) | 2000-03-30 |
ATE283321T1 (de) | 2004-12-15 |
US6565979B1 (en) | 2003-05-20 |
EP1124907A1 (de) | 2001-08-22 |
EP1124907B1 (de) | 2004-11-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0608773B2 (de) | Verfahren zur Herstellung von wässrigen Überzugsmitteln unter Verwendung von Modulsystemen | |
EP0904160B1 (de) | Verfahren zur herstellung von mehrschichtlackierungen auf elektrisch leitfähigen substraten | |
WO1994021730A1 (de) | Füllstoffpaste zur verwendung in basislacken zur beschichtung von polyolefin-substraten, basislacke sowie verfahren zur direktlackierung von polyolefin-substraten | |
WO1995029962A1 (de) | Wässriges überzugsmittel und verfahren zur herstellung von mehrschichtlackierungen mit vom betrachtungswinkel abhängigem farbeindruck | |
DE10124576A1 (de) | Wäßrige Funktions-Beschichtungsstoffe und integriertes Verfahren zur Herstellung farb- und/oder effektgebender Mehrschichtlackierungen | |
DE19652842A1 (de) | Verfahren zur Herstellung von mehrschichtigen Überzügen | |
DE60117527T2 (de) | Pigmentzubereitungen und damit hergestellte wässrige effektbasislacke | |
EP0614951A2 (de) | Verfahren zur Herstellung von wässrigen unifarbenen Überzugsmitteln, unter Verwendung von Modulsystemen | |
EP1112126B1 (de) | Verfahren zur herstellung zweischichtiger automobildecklackierungen | |
WO1997047402A1 (de) | Verfahren zur herstellung von mehrschichtlackierungen auf elektrisch leitfähigen substraten | |
DE60118049T2 (de) | Verfahren zur Herstellung von Mehrschichtlackierungen unter Verwendung eines Pulverklarlackes auf einer wässrigen Basisschicht | |
EP3325176B1 (de) | Verfahren zur herstellung einer aus füller- und decklackschicht bestehenden beschichtung | |
DE602004000259T2 (de) | Verfahren zum lackieren von Kunststoffgegenständen | |
EP0797633B1 (de) | Wässrige überzugsmittel und deren verwendung bei verfahren zur einschicht- und mehrschichtlackierung | |
DE60102045T2 (de) | Wässrige Grundlackzusammensetzungen und Verfahren zur Herstellung von zwei-Schicht wässrigen Grundlack/Klarlack Beschichtungen | |
WO1995029961A1 (de) | Überzugsmittel mit vom betrachtungswinkel abhängigem farbeindruck und deren einsatz in basislacken für mehrschichtlackierungen | |
DE19529394C2 (de) | Verfahren zur Herstellung von Mehrschichtlackierungen auf Metallsubstraten | |
EP3325177B1 (de) | Aus füller und decklack bestehende beschichtungsstoffkombination | |
EP1124907B1 (de) | Zweischichtlackierung aus wässrigem basislack und klarlack mit verbesserter klarlackbenetzungsgrenze | |
DE19754182C2 (de) | Wäßrige Schichtsilikatdispersionen und deren Verwendung bei der Herstellung rheologieoptimierter wäßriger Überzugsmittel | |
WO2000029492A2 (de) | Verfahren zur herstellung von mehrschichtlackierungen | |
DE10060399A1 (de) | Wäßriger, effektgebender Beschichtungsstoff, Verfahren zu seiner Herstellung und seine Verwendung | |
DE19628361A1 (de) | Verfahren zur Herstellung von Mehrschichtlackierungen auf elektrisch leitfähigen Substraten | |
EP4186951A1 (de) | Verfahren zur herstellung einer mehrschichtlackierung | |
EP0591681A1 (de) | Verfahren zur Beschichtung von Kunststoffsubstraten mit Uni- und Effektbasislacken |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): JP US |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE |
|
DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
WWE | Wipo information: entry into national phase |
Ref document number: 1999944583 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 09786505 Country of ref document: US |
|
WWP | Wipo information: published in national office |
Ref document number: 1999944583 Country of ref document: EP |
|
WWG | Wipo information: grant in national office |
Ref document number: 1999944583 Country of ref document: EP |