EP0525867A1 - Two-layer coating systems for wheels and architectural applications - Google Patents
Two-layer coating systems for wheels and architectural applications Download PDFInfo
- Publication number
- EP0525867A1 EP0525867A1 EP92202190A EP92202190A EP0525867A1 EP 0525867 A1 EP0525867 A1 EP 0525867A1 EP 92202190 A EP92202190 A EP 92202190A EP 92202190 A EP92202190 A EP 92202190A EP 0525867 A1 EP0525867 A1 EP 0525867A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- coating layer
- layer
- coating
- resin
- coating system
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
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
- B05D7/50—Multilayers
- B05D7/52—Two layers
- B05D7/53—Base coat plus clear coat type
- B05D7/532—Base coat plus clear coat type the two layers being cured or baked together, i.e. wet on wet
-
- 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
- B05D5/00—Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures
- B05D5/06—Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures to obtain multicolour or other optical effects
- B05D5/067—Metallic effect
- B05D5/068—Metallic effect achieved by multilayers
-
- 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
- B05D7/536—Base coat plus clear coat type each layer being cured, at least partially, separately
-
- 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
- B05D2451/00—Type of carrier, type of coating (Multilayers)
-
- 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
- B05D2601/00—Inorganic fillers
- B05D2601/02—Inorganic fillers used for pigmentation effect, e.g. metallic effect
- B05D2601/04—Mica
Definitions
- the present invention relates to a multilayer coating system which is suitable, e.g., for covering wheels for cars or for use in architectural applications, particularly involving aluminum substrates.
- Such coating systems should possess a good combination of properties such as total layer thickness, metallic lustre, stone-chipping resistance, corrosion resistance, petrol resistance and outdoor durability.
- Known systems are normally based upon at least three coating layers including a first coating layer which provides generally the basic color and opacifying of the substrate, a second liquid layer which provides a metallized effect and, finally, a third liquid clear varnish which provides certain appearance and protective aspects required for the particular end use.
- the known systems do not always possess a desired combination of the aforementioned properties and, in addition, the application of so many coating layers can result in technical problems.
- an object of the present invention to provide a two-layer coating system which surprisingly possesses a more desirable combination of the aforementioned properties.
- the two-layer coating systems in according with the present invention consist essentially of:
- This coating system results in a desirable combination of properties such as weatherability, corrosion resistance, stone-chipping resistance and appearance characteristics.
- the first coating layer in accordance with the present invention provides the basic color of the two-layer coating system as well as opacifying of the substrate.
- the first coating layer may comprise a cathodic electrodeposition coating layer or a powder coating layer based on an epoxy resin, alkyd resin, polyester resin, melamine-containing resin, polyurethane resin and/or polyacrylate resin, such layers and resins being generally well-known in the art.
- the second metallized transparent powder coating layer is preferably based upon any one of a number of polyester resins, epoxy resins, acrylate resins and/or polyurethane resins known for use in powder coatings for producing transparent layers, and optionally a curing agent for that resin.
- polyester resins are particularly preferred.
- the polyester resin can be a hydroxylated polyester in combination with a hydroxyl group reactive curing agent, but preferably is a carboxylated polyester in combination with a carboxyl group reactive curing agent.
- a very suitable powder coating system for the second layer comprises a carboxylated polyester and an epoxy compound as curing agent.
- Suitable polyesters can be obtained via customary preparation processes from by preference substantially aromatic polycarboxylic acids and a variety of polyols.
- aromatic polycaboxylic acids may be mentioned phthalic acid, isophthalic acid, terephthalic acid, pyromellitic acid, trimellitic acid, 3,6-dich- lorophthalic acid, terechlorophthalic acid and, in so far as available, the anhydrides, acid chlorides and lower alkyl esters thereof.
- cycloaliphatic and/or acylic polycarboxylic acids may be utilized in amounts up to 30 mol%, and preferably up to 20 mol%, based upon the total moles of carboxylic acids utilized.
- cycloaliphatic and/or acyclic polycarboxylic acids may be mentioned tetrahydrophthalic acid, hexahydroendomethylene tetrahydrophthalic acid, azeleic acid, sebacic acid, decanedicarboxylic acid, dimeric fatty acids, adipic acid, succinic acid and maleic acid.
- Hydroxycarboxylic acids and/or lactones such as 12-hydroxystearic, E -caprolactone and the hydropivalic acid ester of neopentyl glycol, as well as monocarboxylic acids such as benzoic acid, tert.-butyl benzoic acid, hexahydrobenzoic acid and saturated aliphatic monocarboxylic acids, can also be utilized in minor amounts.
- aliphatic diols such as ethylene glycol, propane-1,2-diol, propane-1,3-diol, butane-1,2-diol, butane-1,4-diol, butane-1,3-diol, 2,2-dimethyl propane-1,3-diol (neopentyl glycol), hexane-2,5-diol, hexane-1,6-diol and diethylene glycol; and cycloaliphatic and aromatic diols such as 1,4-dimethylol cyclohexane, 2,2-bis(4-hydroxycyclohexyl) propane and 2,2-bis-[4-(2-hydroxyethoxy)phenyl] propane.
- aliphatic diols such as ethylene glycol, propane-1,2-diol, propane-1,3-diol, butane-1,2-diol, butane-1,4-diol, butan
- polyol component comprises at least 50 mol% of neopentyl glycol and/or propylene glycol, mol% here being based upon the total moles of polyols utilized.
- the polyesters may be prepared by esterification and/or transesterification, optionally in the presence of customary catalyst such as, for instance, dibutyl tin oxide or tetrabutyltitanate, in which processes, owing to a suitable choice of the preparation conditions and of the COOH/OH ratio, end products are obtained the acid value of which is preferably between 5 and 150 (mg KOH/g resin), and which are preferably carboxyl group terminated.
- customary catalyst such as, for instance, dibutyl tin oxide or tetrabutyltitanate
- the preferred curing agent for the carboxylated polyester is an epoxy compound such as triglycidylisocyanurate or a heterocyclic triepoxy compound, such as methyl- substituted triglycidylisocyanurate or 1,2,4- triglycidyltriazolidine-3,5-dion or diglycidyl-terephthalate or an epoxy resin based on bisphenol A and epichlorohydrin, of which triglycidylisocyanurate is preferred.
- the amount of epoxy compound utilized depends on the acid value of the polyester resin and on the epoxy equivalent weight of the epoxy compound.
- the epoxy compound is utilized in amounts ranging between 0,8 and 1,2 equivalent epoxy per equivalent carboxyl group.
- the second metallized transparent powder coating layer contains a mica pigment which is responsible for the metallization.
- Mica is a well known class of minerals. Most micas are predominantly aluminium silicates of potassium, iron, lithium or fluorine. Since the chemical compositions are quite variable, mica may range from colorless and transparent to highly coloured, opaque varieties. According to a preferred embodiment of the present invention, the mica comprises platelets of mica coated with titanium dioxide.
- the amount of mica utilized in the second layer is between 0,5 and 10% by weight based upon the total weight of the second layer.
- carboxylated polyesters are mixed via, for example, extrusion and at a temperature of from 110-1300 C, with a polyepoxide, eventually pigments and other additives.
- the mica pigment which is responsible for the metallization can be added at different places in the powder coating preparation.
- the addition can take place as an internal metallization before the extrusion, as an external metallization after grinding or a combination of the external and internal metallization.
- the external metallization is used.
- Suitable pigments are, for instance, inorganic pigments such as titanium dioxide, zinc sulphide, iron oxide and chromium oxide, and organic pigments such as azo compounds.
- Suitable fillers are, for instance, quartz powder, calcium and magnesium silicates, calcium carbonate, barium sulphate, calcium sulphate and aluminium oxide and mixtures of these optionally with smaller amounts of, e.g., aluminium hydroxide, am- moniumpolyphosphate and the like.
- Suitable flow-promoting agents are, for instance, liquid polyacrylates such as, for instance, polybutylacrylate and polyethylacrylate, fluorinated polymers such as, for instance, esters of polyethylene glycol and perfluoroctanoic acid and polymeric siloxanes such as, for instance, polydimethyl siloxane or polymethylphenyl siloxane.
- the powder coatings utilized for the second coating layer are preferably applied to the first coating layer by electrostatic/tribo spraying and cured at temperatures between 160-200 °C under the influence of a catalyst. During the curing process, the powder coating melts and subsequently flows out to form a smooth, continuous coating film before substantial curing of the components.
- Suitable catalysts must guarantee rapid curing of the components but must be substantially inactive in the mixing of the polyester and epoxy resins.
- the first layer Prior to application of the second coating layer, the first layer can be a cured layer but also a non-or partially cured layer.
- An advantage of the present two-layer coating system is the possibility to cure both layers in one step, in which case the first layer is applied as a base, over which the second metallized transparent powder coating is applied, after which the total system is cured under the aforementioned conditions.
- the two-layer coating system according to the invention is applied onto an aluminum substrate; however, the system can also be applied on other substrates such as iron, steel, copper, carbon, wood, glass and polymers.
- a cathodic electrodeposition layer as the first layer, especially one based upon an epoxy resin and optional curing agent therefor.
- a cathodic electrodeposition layer based upon an aqueous dispersion or solution of an epoxy resin.
- the thickness of the cathodic electrodeposition first layer is between 15 and 30 ⁇ m
- the thickness of the second metallized transparent powder coating layer is between 30 and 100 ⁇ m (and more preferably between 40 and 70 /1.m)
- the total thickness of the two-layer system is between 45 and 130 ⁇ m (and more preferably between 55 and 100 /1.m).
- the two-layer coating system When the two-layer coating system is utilized in architectural applications, it has been found most advantageous to utilize as the first layer another powder coating based on an epoxy resin, polyester resin, polyacrylate resin and/or polyurethane resin, and optionally a curing agent therefor.
- This first powder coating layer can contain the already mentioned customary additives, and especially a pigment to obtain a color.
- the thickness of the first powder coating layer is between 30 and 100 ⁇ m (and more preferably between 40 and 70 ⁇ m), and the thickness of the second metallized transparent powder coating layer is between 30 and 100 ⁇ m (and more preferably between 40 and 70 ⁇ m).
- a wheel was provided with a cathodic electrodeposition layer based on an epoxy resin.
- a powder coating based on a polyester and TGIC weight ratio polyester: TGIC 93 : 7 and mica ('Mearlin superwhite') was applied in a weight ratio polyester/TGIC: Mica 95 : 5 by tribospraying in a layer thickness of 45 /1.m.
- Curing conditions 10 minutes, 180°C, infrared curing.
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Laminated Bodies (AREA)
- Paints Or Removers (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Abstract
Description
- The present invention relates to a multilayer coating system which is suitable, e.g., for covering wheels for cars or for use in architectural applications, particularly involving aluminum substrates.
- Such coating systems should possess a good combination of properties such as total layer thickness, metallic lustre, stone-chipping resistance, corrosion resistance, petrol resistance and outdoor durability.
- Known systems are normally based upon at least three coating layers including a first coating layer which provides generally the basic color and opacifying of the substrate, a second liquid layer which provides a metallized effect and, finally, a third liquid clear varnish which provides certain appearance and protective aspects required for the particular end use. The known systems, however, do not always possess a desired combination of the aforementioned properties and, in addition, the application of so many coating layers can result in technical problems.
- It is, therefore, an object of the present invention to provide a two-layer coating system which surprisingly possesses a more desirable combination of the aforementioned properties.
- The two-layer coating systems in according with the present invention consist essentially of:
- (a) a first coating layer based on an epoxy resin, alkyd resin, polyester resin, melamine-containing resin, polyurethane resin and/or polyacrylate resin; and
- (b) a second metallized transparent powder coating layer containing a mica pigment.
- The use of this coating system results in a desirable combination of properties such as weatherability, corrosion resistance, stone-chipping resistance and appearance characteristics.
- The first coating layer in accordance with the present invention provides the basic color of the two-layer coating system as well as opacifying of the substrate. Depending on the desired end use, the first coating layer may comprise a cathodic electrodeposition coating layer or a powder coating layer based on an epoxy resin, alkyd resin, polyester resin, melamine-containing resin, polyurethane resin and/or polyacrylate resin, such layers and resins being generally well-known in the art.
- The second metallized transparent powder coating layer is preferably based upon any one of a number of polyester resins, epoxy resins, acrylate resins and/or polyurethane resins known for use in powder coatings for producing transparent layers, and optionally a curing agent for that resin. Of these, the polyester resins are particularly preferred.
- The polyester resin can be a hydroxylated polyester in combination with a hydroxyl group reactive curing agent, but preferably is a carboxylated polyester in combination with a carboxyl group reactive curing agent. A very suitable powder coating system for the second layer comprises a carboxylated polyester and an epoxy compound as curing agent.
- Suitable polyesters can be obtained via customary preparation processes from by preference substantially aromatic polycarboxylic acids and a variety of polyols.
- As aromatic polycaboxylic acids may be mentioned phthalic acid, isophthalic acid, terephthalic acid, pyromellitic acid, trimellitic acid, 3,6-dich- lorophthalic acid, terechlorophthalic acid and, in so far as available, the anhydrides, acid chlorides and lower alkyl esters thereof.
- In addition to the aromatic acids, cycloaliphatic and/or acylic polycarboxylic acids may be utilized in amounts up to 30 mol%, and preferably up to 20 mol%, based upon the total moles of carboxylic acids utilized. As examples of cycloaliphatic and/or acyclic polycarboxylic acids may be mentioned tetrahydrophthalic acid, hexahydroendomethylene tetrahydrophthalic acid, azeleic acid, sebacic acid, decanedicarboxylic acid, dimeric fatty acids, adipic acid, succinic acid and maleic acid. Hydroxycarboxylic acids and/or lactones such as 12-hydroxystearic, E-caprolactone and the hydropivalic acid ester of neopentyl glycol, as well as monocarboxylic acids such as benzoic acid, tert.-butyl benzoic acid, hexahydrobenzoic acid and saturated aliphatic monocarboxylic acids, can also be utilized in minor amounts.
- As suitable polyols may be mentioned aliphatic diols such as ethylene glycol, propane-1,2-diol, propane-1,3-diol, butane-1,2-diol, butane-1,4-diol, butane-1,3-diol, 2,2-dimethyl propane-1,3-diol (neopentyl glycol), hexane-2,5-diol, hexane-1,6-diol and diethylene glycol; and cycloaliphatic and aromatic diols such as 1,4-dimethylol cyclohexane, 2,2-bis(4-hydroxycyclohexyl) propane and 2,2-bis-[4-(2-hydroxyethoxy)phenyl] propane. In addition, smaller amounts of higher functional polyols may also be utilized such as glycerol, hexanetriol, pentaerythritol, sorbitol, trimethylol ethane, trimethylol propane and tris-(2-hydroxy)isocyanurate. Epoxy compounds may also be utilized as polyols. Preferably, the polyol component comprises at least 50 mol% of neopentyl glycol and/or propylene glycol, mol% here being based upon the total moles of polyols utilized.
- Using processes known per se the polyesters may be prepared by esterification and/or transesterification, optionally in the presence of customary catalyst such as, for instance, dibutyl tin oxide or tetrabutyltitanate, in which processes, owing to a suitable choice of the preparation conditions and of the COOH/OH ratio, end products are obtained the acid value of which is preferably between 5 and 150 (mg KOH/g resin), and which are preferably carboxyl group terminated.
- As indicated above, the preferred curing agent for the carboxylated polyester is an epoxy compound such as triglycidylisocyanurate or a heterocyclic triepoxy compound, such as methyl- substituted triglycidylisocyanurate or 1,2,4- triglycidyltriazolidine-3,5-dion or diglycidyl-terephthalate or an epoxy resin based on bisphenol A and epichlorohydrin, of which triglycidylisocyanurate is preferred. The amount of epoxy compound utilized depends on the acid value of the polyester resin and on the epoxy equivalent weight of the epoxy compound. Preferably, the epoxy compound is utilized in amounts ranging between 0,8 and 1,2 equivalent epoxy per equivalent carboxyl group.
- As also indicated above, the second metallized transparent powder coating layer contains a mica pigment which is responsible for the metallization. Mica is a well known class of minerals. Most micas are predominantly aluminium silicates of potassium, iron, lithium or fluorine. Since the chemical compositions are quite variable, mica may range from colorless and transparent to highly coloured, opaque varieties. According to a preferred embodiment of the present invention, the mica comprises platelets of mica coated with titanium dioxide.
- Preferably the amount of mica utilized in the second layer is between 0,5 and 10% by weight based upon the total weight of the second layer.
- The preparation of powder coatings based upon carboxylated polyesters and epoxy resins is generally well-known in the art. Preferably, the carboxylated polyesters are mixed via, for example, extrusion and at a temperature of from 110-1300 C, with a polyepoxide, eventually pigments and other additives.
- The mica pigment which is responsible for the metallization can be added at different places in the powder coating preparation. The addition can take place as an internal metallization before the extrusion, as an external metallization after grinding or a combination of the external and internal metallization. Peferably the external metallization is used.
- Other normal additives such as, for instance, other pigments, fillers, anti-oxidants, colorants, flow-promoting agents, release agents, viscosity agents, levelling agents and UV-stabilizers can be added to the coating systems of the two-layers.
- Suitable pigments are, for instance, inorganic pigments such as titanium dioxide, zinc sulphide, iron oxide and chromium oxide, and organic pigments such as azo compounds.
- Suitable fillers are, for instance, quartz powder, calcium and magnesium silicates, calcium carbonate, barium sulphate, calcium sulphate and aluminium oxide and mixtures of these optionally with smaller amounts of, e.g., aluminium hydroxide, am- moniumpolyphosphate and the like.
- Suitable flow-promoting agents are, for instance, liquid polyacrylates such as, for instance, polybutylacrylate and polyethylacrylate, fluorinated polymers such as, for instance, esters of polyethylene glycol and perfluoroctanoic acid and polymeric siloxanes such as, for instance, polydimethyl siloxane or polymethylphenyl siloxane.
- Of course, with respect to the second coating layer these additives should not substantially affect the transparent nature thereof.
- The powder coatings utilized for the second coating layer are preferably applied to the first coating layer by electrostatic/tribo spraying and cured at temperatures between 160-200 °C under the influence of a catalyst. During the curing process, the powder coating melts and subsequently flows out to form a smooth, continuous coating film before substantial curing of the components.
- Suitable catalysts must guarantee rapid curing of the components but must be substantially inactive in the mixing of the polyester and epoxy resins.
- Prior to application of the second coating layer, the first layer can be a cured layer but also a non-or partially cured layer. An advantage of the present two-layer coating system, however, is the possibility to cure both layers in one step, in which case the first layer is applied as a base, over which the second metallized transparent powder coating is applied, after which the total system is cured under the aforementioned conditions.
- Preferably the two-layer coating system according to the invention is applied onto an aluminum substrate; however, the system can also be applied on other substrates such as iron, steel, copper, carbon, wood, glass and polymers.
- When the two-layer coating system is applied onto wheels for cars, it has been found most advantageous to utilize a cathodic electrodeposition layer as the first layer, especially one based upon an epoxy resin and optional curing agent therefor. Particularly preferred is a cathodic electrodeposition layer based upon an aqueous dispersion or solution of an epoxy resin.
- Preferably, the thickness of the cathodic electrodeposition first layer is between 15 and 30 µm, the thickness of the second metallized transparent powder coating layer is between 30 and 100 µm (and more preferably between 40 and 70 /1.m), and the total thickness of the two-layer system is between 45 and 130 µm (and more preferably between 55 and 100 /1.m).
- When the two-layer coating system is utilized in architectural applications, it has been found most advantageous to utilize as the first layer another powder coating based on an epoxy resin, polyester resin, polyacrylate resin and/or polyurethane resin, and optionally a curing agent therefor.
- This first powder coating layer can contain the already mentioned customary additives, and especially a pigment to obtain a color.
- Preferably, the thickness of the first powder coating layer is between 30 and 100 µm (and more preferably between 40 and 70 µm), and the thickness of the second metallized transparent powder coating layer is between 30 and 100 µm (and more preferably between 40 and 70 µm).
- This system results in an excellent aspect of the powder layer for architectural uses. Furthermore the adhesion between the two layers is very good.
- The invention will be further elucidated by means of the following examples, without, however, being limited thereto.
- A wheel was provided with a cathodic electrodeposition layer based on an epoxy resin. Next, a powder coating based on a polyester and TGIC (weight ratio polyester: TGIC 93 : 7) and mica ('Mearlin superwhite') was applied in a weight ratio polyester/TGIC: Mica 95 : 5 by tribospraying in a layer thickness of 45 /1.m.
- Curing conditions: 10 minutes, 180°C, infrared curing.
- The coating system resulted in the following characteristics:
- - weatherability (according to the Peugeot method; xenon with 500 hours exposure) : loss of gloss 2%
- - salt spray resistance (ASTM B 117) 800 hours: disbonding less than 0,5 mm, no blistering
- - stone-chipping resistance (Peugeot method) : 1 (1 = excellent, 2 = very good, whereas 10 = very bad).
Claims (14)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP91201959 | 1991-07-26 | ||
EP91201959 | 1991-07-26 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0525867A1 true EP0525867A1 (en) | 1993-02-03 |
EP0525867B1 EP0525867B1 (en) | 1995-12-06 |
Family
ID=8207802
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP19920202190 Expired - Lifetime EP0525867B1 (en) | 1991-07-26 | 1992-07-17 | Two-layer coating systems for wheels and architectural applications |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP0525867B1 (en) |
CA (1) | CA2074661A1 (en) |
DE (1) | DE69206509T2 (en) |
ES (1) | ES2080432T3 (en) |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0646420A1 (en) * | 1993-09-17 | 1995-04-05 | Herberts Gesellschaft mit beschränkter Haftung | Process for making multilayer coatings |
FR2715160A1 (en) * | 1994-01-19 | 1995-07-21 | Montupet Sa | Wheel or body element or metal accessory, for a motor vehicle, coated with an iridescent metallic paint and method of manufacture. |
WO1997030796A1 (en) * | 1996-02-23 | 1997-08-28 | Basf Coatings Ag | Process for the multi-layered coating of substrates with electrophoretic coating material and powder coating material |
GB2328628A (en) * | 1997-08-27 | 1999-03-03 | Nippon Paint Co Ltd | Powder coating method |
GB2342600A (en) * | 1998-10-08 | 2000-04-19 | Thorstone Business Man Ltd | Coatings |
US6068890A (en) * | 1996-07-31 | 2000-05-30 | Dr. Ing. H.C.F. Porsche Ag | Method for gloss coating articles |
GB2369790A (en) * | 2000-12-08 | 2002-06-12 | Northpoint Ltd | Method of protecting a surface |
US6413588B1 (en) | 1999-01-11 | 2002-07-02 | E. I. Du Pont De Nemours And Company | Method of producing durable layered coatings |
GB2379897A (en) * | 2001-08-31 | 2003-03-26 | Kansai Paint Co Ltd | Multilayer decorative coating including electrodeposited layer |
US6641666B2 (en) | 1999-11-15 | 2003-11-04 | Ppg Industries Ohio, Inc. | Method and apparatus for coating a substrate |
WO2005120724A1 (en) * | 2004-06-05 | 2005-12-22 | Basf Coatings Ag | Method for coating electrically conductive substrates |
US7445816B2 (en) | 1999-11-15 | 2008-11-04 | Ppg Industries Ohio, Inc. | Method and apparatus for coating a substrate |
EP2153911A1 (en) * | 2008-08-05 | 2010-02-17 | Pulverit S.p.A. | Painting/coating process using a powder primer with high reactivity, polymerisable in a single step with the finishing coat |
WO2018226421A1 (en) * | 2017-06-07 | 2018-12-13 | Novelis Inc. | Multi-layered finishes for can ends |
IT202000005629A1 (en) * | 2020-03-17 | 2021-09-17 | La Bottega S R L | "METHOD OF PRODUCTION OF AN OBJECT COVERED WITH A PAINTED LAYER" |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1769867A1 (en) * | 1968-07-27 | 1971-02-11 | Metallgesellschaft Ag | Process for the production of colored plastic coatings |
DE3324726A1 (en) * | 1983-07-08 | 1985-01-17 | Bosch-Siemens Hausgeräte GmbH, 7000 Stuttgart | Process for the production of a multi-layer coating on a substrate to be coated by powder coating in an electrostatic field |
EP0186607A1 (en) * | 1984-12-11 | 1986-07-02 | Basf Corporation | Multilayer satin finish automotive paint system |
DE3814853A1 (en) * | 1987-05-02 | 1988-11-10 | Kansai Paint Co Ltd | COATING PROCESS |
-
1992
- 1992-07-17 DE DE1992606509 patent/DE69206509T2/en not_active Expired - Fee Related
- 1992-07-17 EP EP19920202190 patent/EP0525867B1/en not_active Expired - Lifetime
- 1992-07-17 ES ES92202190T patent/ES2080432T3/en not_active Expired - Lifetime
- 1992-07-24 CA CA 2074661 patent/CA2074661A1/en not_active Abandoned
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1769867A1 (en) * | 1968-07-27 | 1971-02-11 | Metallgesellschaft Ag | Process for the production of colored plastic coatings |
DE3324726A1 (en) * | 1983-07-08 | 1985-01-17 | Bosch-Siemens Hausgeräte GmbH, 7000 Stuttgart | Process for the production of a multi-layer coating on a substrate to be coated by powder coating in an electrostatic field |
EP0186607A1 (en) * | 1984-12-11 | 1986-07-02 | Basf Corporation | Multilayer satin finish automotive paint system |
DE3814853A1 (en) * | 1987-05-02 | 1988-11-10 | Kansai Paint Co Ltd | COATING PROCESS |
Cited By (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0646420A1 (en) * | 1993-09-17 | 1995-04-05 | Herberts Gesellschaft mit beschränkter Haftung | Process for making multilayer coatings |
FR2715160A1 (en) * | 1994-01-19 | 1995-07-21 | Montupet Sa | Wheel or body element or metal accessory, for a motor vehicle, coated with an iridescent metallic paint and method of manufacture. |
EP0664163A1 (en) * | 1994-01-19 | 1995-07-26 | Montupet S.A. | Wheel, vehicle body element or metallic part, for vehicles, coated with metallic iridescent paint and process for manufacturing it |
WO1997030796A1 (en) * | 1996-02-23 | 1997-08-28 | Basf Coatings Ag | Process for the multi-layered coating of substrates with electrophoretic coating material and powder coating material |
US6254751B1 (en) | 1996-02-23 | 2001-07-03 | Basf Coatings Ag | Process for the multi-layered coating of substrates with electrophoretic coating material and powder coating material |
US6068890A (en) * | 1996-07-31 | 2000-05-30 | Dr. Ing. H.C.F. Porsche Ag | Method for gloss coating articles |
US6238786B1 (en) | 1996-07-31 | 2001-05-29 | Dr. Ing. H.C.F. Porsche Ag | Method for gloss coating articles |
GB2328628A (en) * | 1997-08-27 | 1999-03-03 | Nippon Paint Co Ltd | Powder coating method |
US6025035A (en) * | 1997-08-27 | 2000-02-15 | Nippon Paint Co., Ltd. | Electrostatic coating method and coating film |
GB2328628B (en) * | 1997-08-27 | 2001-10-10 | Nippon Paint Co Ltd | Paint film-forming method and paint film |
GB2342600A (en) * | 1998-10-08 | 2000-04-19 | Thorstone Business Man Ltd | Coatings |
GB2342600B (en) * | 1998-10-08 | 2003-03-19 | Thorstone Business Man Ltd | Coatings |
US6413588B1 (en) | 1999-01-11 | 2002-07-02 | E. I. Du Pont De Nemours And Company | Method of producing durable layered coatings |
US6641666B2 (en) | 1999-11-15 | 2003-11-04 | Ppg Industries Ohio, Inc. | Method and apparatus for coating a substrate |
US7445816B2 (en) | 1999-11-15 | 2008-11-04 | Ppg Industries Ohio, Inc. | Method and apparatus for coating a substrate |
GB2369790A (en) * | 2000-12-08 | 2002-06-12 | Northpoint Ltd | Method of protecting a surface |
GB2379897A (en) * | 2001-08-31 | 2003-03-26 | Kansai Paint Co Ltd | Multilayer decorative coating including electrodeposited layer |
GB2379897B (en) * | 2001-08-31 | 2005-07-13 | Kansai Paint Co Ltd | Method for forming multilayer coating film |
WO2005120724A1 (en) * | 2004-06-05 | 2005-12-22 | Basf Coatings Ag | Method for coating electrically conductive substrates |
US7862851B2 (en) | 2004-06-05 | 2011-01-04 | Basf Coatings Ag | Process for coating electrically conductive substrates |
EP2153911A1 (en) * | 2008-08-05 | 2010-02-17 | Pulverit S.p.A. | Painting/coating process using a powder primer with high reactivity, polymerisable in a single step with the finishing coat |
WO2018226421A1 (en) * | 2017-06-07 | 2018-12-13 | Novelis Inc. | Multi-layered finishes for can ends |
US11065843B2 (en) | 2017-06-07 | 2021-07-20 | Novelis Inc. | Multi-layered finishes for can ends |
IT202000005629A1 (en) * | 2020-03-17 | 2021-09-17 | La Bottega S R L | "METHOD OF PRODUCTION OF AN OBJECT COVERED WITH A PAINTED LAYER" |
Also Published As
Publication number | Publication date |
---|---|
EP0525867B1 (en) | 1995-12-06 |
DE69206509D1 (en) | 1996-01-18 |
DE69206509T2 (en) | 1996-08-01 |
CA2074661A1 (en) | 1993-01-27 |
ES2080432T3 (en) | 1996-02-01 |
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