EP0320552A1 - Verfahren zur Verbesserung des Aussehens eines mehrschichtigen Überzugs - Google Patents

Verfahren zur Verbesserung des Aussehens eines mehrschichtigen Überzugs Download PDF

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Publication number
EP0320552A1
EP0320552A1 EP87311191A EP87311191A EP0320552A1 EP 0320552 A1 EP0320552 A1 EP 0320552A1 EP 87311191 A EP87311191 A EP 87311191A EP 87311191 A EP87311191 A EP 87311191A EP 0320552 A1 EP0320552 A1 EP 0320552A1
Authority
EP
European Patent Office
Prior art keywords
coating composition
guide
weight
process according
base
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.)
Withdrawn
Application number
EP87311191A
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English (en)
French (fr)
Inventor
David Chi Kung Chang
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to US06/906,195 priority Critical patent/US4731290A/en
Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Priority to EP87311191A priority patent/EP0320552A1/de
Publication of EP0320552A1 publication Critical patent/EP0320552A1/de
Withdrawn legal-status Critical Current

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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D7/00Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
    • B05D7/50Multilayers
    • B05D7/56Three layers or more
    • B05D7/57Three layers or more the last layer being a clear coat
    • B05D7/572Three layers or more the last layer being a clear coat all layers being cured or baked together
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D5/00Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures
    • B05D5/06Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures to obtain multicolour or other optical effects
    • B05D5/067Metallic effect
    • B05D5/068Metallic effect achieved by multilayers

Definitions

  • This invention is related to an improved process for forming multilayer finishes on automobiles and trucks.
  • the process forms finishes that have an improved appearance.
  • Multilayer finishes in particular, clear coat/base coat finishes are well known in the art, as shown, for example, in Benefiel et al US 3,639,147, issued February 1, 1972.
  • solvent based coating compositions have been used to form these multilayer finishes.
  • water borne base coat finishes in combination with either solvent based or water based clear coat finishes are being tested for use.
  • improvements in head-on-brightness would be desired.
  • This invention provides an improved process and a composition that can be applied by this process to form a clear coat/base coat finish with water borne base coating compositions containing metallic flake pigments that have a high quality appearance that is acceptable to the automotive industry.
  • This invention is directed to an improved process for applying a multilayer finish to a substrate that has a primer layer adhered thereto and a layer of a water borne base coating composition containing metallic flake pigments and a layer of a clear top coating composition; the improvement that is used with this process comprises the following: applying a layer of a waterborne guide coating composition containing an aqueous carrier and a polymeric binder to the primer layer before application of the water borne base coating composition and drying the guide coating at ambient temperatures or at an elevated temperature without crosslinking or curing the guide coating and then applying the waterborne base coating composition to the guide coating and clear top coating composition to the base coating and baking at elevated temperatures to fully cure the resulting multilayer finish; whereby the resulting multilayer finish on the substrate comprising the guide coating, base coating and clear topcoating has an improved appearance.
  • the improved process of this invention is used to improved the appearance of a water borne base coating composition/clear coating composition used for automobiles and trucks.
  • a guide coating is applied over the primer coating of the substrate and then dried but not cured.
  • the guide coat can be dried at ambient temperatures e.g. 20-25°C or baked at elevated temperatures up to 180°C for a short time or exposed to infrared radiation for rapid drying taking care not to crosslink the guide coat.
  • the water borne base coating is applied over the guide coating and then the clear coating composition is applied over the base coating and the resulting coated substrate is baked at an elevated temperature to form a fully cured multilayer finish.
  • the resulting base coat/clear coat finish has an improved appearance, particularly for head-on-brightness, in comparison to clear coat/color coat finishes that do not use a guiding coating composition.
  • the guide coating composition is an aqueous based composition containing about 10-75% by weight of a film forming binder and preferably, a crosslinking agent and pigments.
  • a crosslinking agent and pigments typically, an aqueous latex is used as the film forming binder and preferably, an acrylic latex is used.
  • An alkylated melamine formaldehyde crosslinking agent can be used in the composition. Any of the conventional pigments used for coating compositions or primers can be used in the composition.
  • the binder of the guide coating composition is an acrylic latex but other water dispersible or water soluble polymers can be used.
  • the latex is prepared by a conventional emulsion polymerization process in which monomers, a polymerization catalyst such as ammonium persulfate, water, surfactants and usually a neutralizing agent such as ammonia or an amine such as amino ethyl propanol are utilized.
  • the polymerization is carried out under conventional temperatures of about 50-90°C for about 1-5 hours to form a latex.
  • the monomers used for the latex are alkyl methacrylates, alkyl acrylates, hydroxy alkyl acrylates and methacrylates and an ethylenically unsaturated polymerizable mono or di carboxylic acids. Difunctional acrylates or methacrylates also can be used.
  • Typical alkyl methacrylates are methyl methacrylate, ethyl methacrylate, propyl methacrylate, butyl methacrylate, hexyl methacrylate, octyl methacrylate, nonyl methacrylate, lauryl methacrylate and the like.
  • Typical alkyl acrylates are methyl acrylate, ethyl acrylate, propyl acrylate, butyl acrylate, hexyl acrylate, octyl acrylate, nonyl acrylate, lauryl acrylate and the like.
  • Typical hydroxy alkyl acrylates and hydroxy alkyl methacrylates that can be used are hydroxy ethyl methacrylate, hydroxy propyl methacrylate, hydroxy butyl methacrylate, hydroxy ethyl acrylate, hydroxy propyl acrylate, hydroxy butyl acrylate and the like.
  • Typical polymerizable mono or di carboxlic acids that can be used are methacrylic acid, acrylic acid, itaconic acid, maleic acid and the like.
  • Difunctional monomers that can be used are allyl methacrylate, allyl acrylate and other diacrylates.
  • One preferred latex polymer contains 10-20% by weight methyl methacrylate, 70-80% by weight butyl acrylate, 2-9% by weight hydroxy ethyl acrylate, and 1-5% by weight methacrylic acid.
  • the latex itself without a crosslinking agent can be used as a guide coating composition. This has an advantage that the latex does not crosslink on drying or baking at an elevated temperature.
  • the guide coating contains about 5-40% by weight, based on the weight of the binder, of the crosslinking agent.
  • One preferred composition contains about 5-30% by weight of the crosslinking agent and 70-95% of the latex polymer.
  • Typical monomeric and polymeric alkylated melamine formaldehyde crosslinking agents that can be used are partially or highly methylated melamine formaldehyde resins, such as “Cymel” 300 resins, mixed ether and butylated melamine formalhyde resins or other partially or fully alklated melamine formaldehyde resins having 1-6 carbons in the alkyl group.
  • One preferred resin is "Cymel” 325 which is a methylated melamine formaldehyde resin that has a methoxymethyl-imino functionality.
  • Another preferred resin is "Cymel” 303 which is a highly methylated melamine formaldehyde resin containing reactive alkoxy groups.
  • the guide coating composition can be used as an unpigmented clear but preferably contains pigments in a pigment to binder weight ratio of about 0.5/100 to 300/100.
  • the pigments provide additional hiding and are usually the same as the pigments of the base coating composition.
  • Typical pigments that can be used are titanium dioxide, other metallic oxides such as zinc oxide and iron oxide, carbon black, organic pigments and dyes,metallic flake pigments such as aluminum flake,filler pigments, silica, and the like.
  • the composition contains metallic flake pigments such as aluminum flake.
  • the pigments are formulated into a millbase using conventional procedures and then the mill base is blending with the latex and the crosslinking agent to form the guide coating composition.
  • the substrates over which the guide coat is applied are those conventionally used for automotive and truck bodies such as cold roll steel, phosphatized steel, polyester reinforced fiber glass, reaction injection molded urethanes, crystalline amorphous polyamides and the like. Typically, these substrates are coated with alkyd resin, epoxy resin or polyester primers.
  • the guide coating compositon is applied. Any of the conventional methods of application can be used such as spraying or electrostatic spraying.
  • the coating is applied to provide a dry film thickness of about 0.1 to 1.0 mils.
  • the coating is then dried but not fully cured or crosslinked.
  • the base coating composition is applied by spraying or electrostatic spraying to provide a dry film of about 0.2-1.5 mils thick.
  • a clear coating composition is applied by spraying or electrostatic spraying to a dry film thickness of about 0.5-6.0 mils.
  • the resulting multilayer finish then is baked at about 120-175°C for about 15 minutes - 1 hour to form a glossy finish having excellent head-on-brightness and a good appearance.
  • the base coating composition can be any of the composition that are conventially used such as acrylics or polyesters containing crosslinking agents. These compositions can be solvent or water based solutions or dispersions.
  • the process of this invention is particularly useful for waterborne base coatings containing metallic flake pigments and provides a finish with improved head-on-brightness. However, improvements are noted also with the use of solvent based base coat finishes.
  • the clear coating composition can be a solvent or water based composition of an acrylic or polyester polymer and containing a crosslinking agent or other type of composition as are conventially used for clear coating compositions.
  • the guide coating composition also can be used with two component base coat/clear coat compositions that do not require baking for curing such as two component acrylic urethanes, acrylic esters, acrylic alkyds, epoxy esters and the like. These two component compositions are used to refinish cars and trucks. Application of the guide coating composition is the same as above and then the two component base coating composition and clear coating composition are applied and cured at ambient temperatures or force dried at elevated temperatures.
  • a latex was prepared by charging the following ingredients into a polymerization vessel equipped with a stirrer and a heating source: Portion 1 Parts By Weight Deionized water 2535.0 Alkyl phenol ethylene oxide anionic surfactant 16.4 Portion 2 Anionic surfactant (described above) 23.4 Methyl methacrylate monomer 369.0 Butyl methacrylate monmer 1622.4 Deionized water 2335.0 Portion 3 Deionized water 225.0 Ammonium persulfate 7.0 Portion 4 Deionized water 1097.0 Anionic surfactant (described above) 11.7 Methacrylic acid 81.7 Hydroxy ethyl acrylate monmer 116.8 Butyl acrylate monomer 385.3 Portion 5 Deionized water 85.0 Ammonium persulfate 2.3 Portion 6 Deionized water 451.0 Amino ethyl propanol 60.7 "Cosan" 145 - latex preservative of an oxazolidine derivative
  • Portion 1 is charged into the polymerization vessel and heated to about 83°C.
  • Portion 2 is premixed. About 10% of Portion 2 is added and the resulting reaction mixture is held at about 80°C. About 10% of Portion 3 is added and the reaction mixture is held at the above temperature. The remainder of Portion 2 is added over a 60 minute period along the about 72% of Portion 3 while controlling the reaction mixture at about 85°C. The remainder of Portion 3 along with Portion 4 is added over a 30 minute period while controlling the reaction mixture at 85°C.
  • Portion 5 is added and the reaction mixture is held at about 85°C for 60 minutes.
  • Portion 6 is added over a 30 minute period and held at the above temperature for about 1 hour. The resulting latex is cooled to room temperature and filtered.
  • the latex has a polymer solids content of 27.7% and a pH of 7.2.
  • the polymer is comprised of 14.3% methyl methacrylate, 78.0% butyl acrylate, 3.2% methacrylic acid, and 4.5% hydroxy ethyl acrylate.
  • a mill base was prepared as follows: Parts By Weight Ethylene glycol monobutyl ether 55.13 Polyoxyethylene ester of mixed fatty acids and resins 4.87 Aluminun flake paste - 65% solids aluminuN flake in mineral spirits 40.00 Total 100.00
  • the above constituents are charged into a mixing vessel and thoroughly mixed together.
  • the following guide coating compositions A-C were formulated: COMPOSITION Parts By Weight A B C Latex (prepared above) 1557.0 1557.0 1557.0 Deionized water 488.0 1029.0 1029.0 Melamine formaldehyde resin solution (80% solids in isobutanol of a highly methylated melamine formaldehyde resin having a low methylol content and containing alkoxy imino groups) 104.0 104.0 ------ Mill base (prepared above) 331.0 ---- ---- Deionized water 541.0 ---- ---- Dimethyl ethanol amine 23.4 23.4 23.4 "Acrysol” ASE 60 (Acrylic latex thickener) 28.0 28.0 28.0 Total 3072.4 2741.4 2637.4
  • Each of the above Guide Coating Compositions A-C were sprayed onto separate phosphatized steel panels coated with an epoxy/polyester electrodeposition primer. Each composition was sprayed onto four separate panels. One panel was dried at ambient temperature of about 25°C for about 30 minutes; the second panel was baked for about 2 minutes at about 104°C which was sufficient time to dry the coating but not cure the coating; the third panel was baked for about 10 minutes at about 121°C which was sufficient time to cure the coating and the fourth panel was baked for about 30 minutes at 121°C which was sufficient to cure the coating. In each case the dried Guide Coating was about 0.3 mils thick when dried.
  • a base coating was then applied by spraying a layer of above Composition A to each of the above coated panels and the base coating was dried at ambient temperatures for about 10 minutes to form a dried coating about 0.5 mils thick. Then a clear topcoating was spray applied and the coated panels were baked for about 30 minutes at about 120°C to form a clear coat/base coat finish.
  • the above clear coating composition has a solids content of about 68% in a 50/50 solvent mixture of methyl amyl ketone and aromatic hydrocarbon wherein the polymer comprises styrene/butyl methacrylate/butyl acrylate/hydroxy ethyl acrylate/acrylic acid in a ratio of about 14.9/28/30/25/2.1.
  • a control for each of the guide costs A - C of phosphatized primed steel panel was prepared as above i.e., the panel was coated with the base coat and the clear coat as above, except a guide coat was omitted. Each panel was baked under the same conditions. These panels were used as the controls and represents prior art method of preparing a clear coat/­base coat finish.
  • guide coating C which is the acrylic latex without a crosslinking agent curing does not occur and the desirable improvement by use of this guide coat is noted at all baking temperatures.

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  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)
EP87311191A 1986-09-11 1987-12-18 Verfahren zur Verbesserung des Aussehens eines mehrschichtigen Überzugs Withdrawn EP0320552A1 (de)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US06/906,195 US4731290A (en) 1986-09-11 1986-09-11 Process for improving the appearance of a multilayer finish
EP87311191A EP0320552A1 (de) 1987-12-18 1987-12-18 Verfahren zur Verbesserung des Aussehens eines mehrschichtigen Überzugs

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP87311191A EP0320552A1 (de) 1987-12-18 1987-12-18 Verfahren zur Verbesserung des Aussehens eines mehrschichtigen Überzugs

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EP0320552A1 true EP0320552A1 (de) 1989-06-21

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Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4009000A1 (de) * 1990-03-21 1991-09-26 Basf Lacke & Farben Verfahren zur herstellung einer mehrschichtigen reparaturlackierung
DE4110520A1 (de) * 1991-03-30 1992-10-01 Basf Lacke & Farben Mischsystem zur herstellung wasserverduennbarer ueberzugsmittel
DE19652841A1 (de) * 1995-12-21 1997-06-26 Basf Lacke & Farben Verfahren zur Herstellung von mehrschichtigen Überzügen
DE19638600A1 (de) * 1996-09-20 1998-04-02 Basf Coatings Ag Verfahren zur Herstellung einer mehrschichtigen Reparaturlackierung
US6143367A (en) * 1996-12-18 2000-11-07 Basf Coatings Ag Coating agent and method for producing same
US6225400B1 (en) 1996-12-18 2001-05-01 Basf Coating Ag Coating agent and method for producing same
US6410646B1 (en) 1997-03-07 2002-06-25 Basf Coatings Ag Method for producing scratch resistant coatings, especially for producing multi-layer enamels
US6448326B1 (en) 1991-03-03 2002-09-10 Basf Coatings Ag Mixer system for the preparation of water-thinnable coating compositions
EP0788523B2 (de) 1994-10-28 2002-11-27 BASF Coatings Aktiengesellschaft Verfahren zur Herstellung von mehrschichtigen Lackierungen
US6534185B1 (en) 1998-10-31 2003-03-18 Basf Coatings Ag Coating agent with a macromer unit for the production of multi-layered coatings
US6583214B1 (en) 1999-04-01 2003-06-24 Basf Coatings Ag Aqueous coating material that is cured thermally and/or by actinic radiation, and its use
US6632495B1 (en) 1999-04-01 2003-10-14 Basf Coatings Ag Pyrimidine-based crosslinking agents
US6652919B1 (en) 1999-02-25 2003-11-25 Basf Coatings Ag Highly scratch-resistant multilayer coat, method for producing and use of the same
US6835420B1 (en) 1999-08-16 2004-12-28 Basf Coatings Ac Coating material and its use for producing highly scratch resistant multilayer transparent lacquers
US20080280061A1 (en) * 2007-05-07 2008-11-13 Roger Questel Method for sealing natural stone
EP3815898A1 (de) 2019-10-28 2021-05-05 Covestro Deutschland AG Schichtenverbund aus polycarbonat und polycarbonatblend zur verbesserten lackierbarkeit
US11065843B2 (en) 2017-06-07 2021-07-20 Novelis Inc. Multi-layered finishes for can ends

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3639147A (en) * 1968-09-30 1972-02-01 Celanese Coatings Co Article having multilayer coating and process for producing same
FR2244572A1 (de) * 1973-09-26 1975-04-18 Ici Ltd
US3953643A (en) * 1974-12-20 1976-04-27 Ford Motor Company Method for coating and product
US4303581A (en) * 1980-07-16 1981-12-01 Ppg Industries, Inc. Water dispersed primer-surfacer composition
US4619746A (en) * 1985-10-02 1986-10-28 Ppg Industries, Inc. Process for topcoating an electrocoated substrate with a high solids fluid coating
US4731290A (en) * 1986-09-11 1988-03-15 E. I. Du Pont De Nemours And Company Process for improving the appearance of a multilayer finish

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3639147A (en) * 1968-09-30 1972-02-01 Celanese Coatings Co Article having multilayer coating and process for producing same
FR2244572A1 (de) * 1973-09-26 1975-04-18 Ici Ltd
US3953643A (en) * 1974-12-20 1976-04-27 Ford Motor Company Method for coating and product
US4303581A (en) * 1980-07-16 1981-12-01 Ppg Industries, Inc. Water dispersed primer-surfacer composition
US4619746A (en) * 1985-10-02 1986-10-28 Ppg Industries, Inc. Process for topcoating an electrocoated substrate with a high solids fluid coating
US4731290A (en) * 1986-09-11 1988-03-15 E. I. Du Pont De Nemours And Company Process for improving the appearance of a multilayer finish

Cited By (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4009000A1 (de) * 1990-03-21 1991-09-26 Basf Lacke & Farben Verfahren zur herstellung einer mehrschichtigen reparaturlackierung
US6448326B1 (en) 1991-03-03 2002-09-10 Basf Coatings Ag Mixer system for the preparation of water-thinnable coating compositions
DE4110520A1 (de) * 1991-03-30 1992-10-01 Basf Lacke & Farben Mischsystem zur herstellung wasserverduennbarer ueberzugsmittel
DE4110520C5 (de) * 1991-03-30 2005-10-20 Basf Coatings Ag Mischsystem zur Herstellung wasserverdünnbarer Überzugsmittel
EP0788523B2 (de) 1994-10-28 2002-11-27 BASF Coatings Aktiengesellschaft Verfahren zur Herstellung von mehrschichtigen Lackierungen
DE19652841A1 (de) * 1995-12-21 1997-06-26 Basf Lacke & Farben Verfahren zur Herstellung von mehrschichtigen Überzügen
DE19638600A1 (de) * 1996-09-20 1998-04-02 Basf Coatings Ag Verfahren zur Herstellung einer mehrschichtigen Reparaturlackierung
DE19638600C2 (de) * 1996-09-20 2002-03-07 Basf Coatings Ag Verfahren zur Herstellung einer mehrschichtigen Reparaturlackierung sowie dessen Verwendung
US6143367A (en) * 1996-12-18 2000-11-07 Basf Coatings Ag Coating agent and method for producing same
US6225400B1 (en) 1996-12-18 2001-05-01 Basf Coating Ag Coating agent and method for producing same
US6620884B2 (en) 1997-03-07 2003-09-16 Basf Coatings Ag Method for producing scratch resistant coatings, especially for producing multi-layer enamels
US6410646B1 (en) 1997-03-07 2002-06-25 Basf Coatings Ag Method for producing scratch resistant coatings, especially for producing multi-layer enamels
US6534185B1 (en) 1998-10-31 2003-03-18 Basf Coatings Ag Coating agent with a macromer unit for the production of multi-layered coatings
US6652919B1 (en) 1999-02-25 2003-11-25 Basf Coatings Ag Highly scratch-resistant multilayer coat, method for producing and use of the same
US6632495B1 (en) 1999-04-01 2003-10-14 Basf Coatings Ag Pyrimidine-based crosslinking agents
US6583214B1 (en) 1999-04-01 2003-06-24 Basf Coatings Ag Aqueous coating material that is cured thermally and/or by actinic radiation, and its use
US6835420B1 (en) 1999-08-16 2004-12-28 Basf Coatings Ac Coating material and its use for producing highly scratch resistant multilayer transparent lacquers
US20080280061A1 (en) * 2007-05-07 2008-11-13 Roger Questel Method for sealing natural stone
US11065843B2 (en) 2017-06-07 2021-07-20 Novelis Inc. Multi-layered finishes for can ends
EP3815898A1 (de) 2019-10-28 2021-05-05 Covestro Deutschland AG Schichtenverbund aus polycarbonat und polycarbonatblend zur verbesserten lackierbarkeit
WO2021083925A1 (de) 2019-10-28 2021-05-06 Covestro Intellectual Property Gmbh & Co. Kg Schichtenverbund aus polycarbonat und polycarbonatblend zur verbesserten lackierbarkeit

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