WO2006078425A2 - Polyvinylidene fluoride coating for metal substrates - Google Patents

Polyvinylidene fluoride coating for metal substrates Download PDF

Info

Publication number
WO2006078425A2
WO2006078425A2 PCT/US2005/047118 US2005047118W WO2006078425A2 WO 2006078425 A2 WO2006078425 A2 WO 2006078425A2 US 2005047118 W US2005047118 W US 2005047118W WO 2006078425 A2 WO2006078425 A2 WO 2006078425A2
Authority
WO
WIPO (PCT)
Prior art keywords
percent
weight
coating composition
resin
substrate
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.)
Ceased
Application number
PCT/US2005/047118
Other languages
French (fr)
Other versions
WO2006078425A3 (en
Inventor
Min Zheng
Kurt A. Wood
Scott Gaboury
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.)
Arkema Inc
Original Assignee
Arkema Inc
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
Application filed by Arkema Inc filed Critical Arkema Inc
Priority to EP20050855641 priority Critical patent/EP1838529A2/en
Priority to JP2007552144A priority patent/JP2008528727A/en
Publication of WO2006078425A2 publication Critical patent/WO2006078425A2/en
Anticipated expiration legal-status Critical
Publication of WO2006078425A3 publication Critical patent/WO2006078425A3/en
Ceased legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D127/00Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers
    • C09D127/02Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
    • C09D127/12Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
    • C09D127/16Homopolymers or copolymers of vinylidene fluoride
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/36Sulfur-, selenium-, or tellurium-containing compounds
    • C08K5/41Compounds containing sulfur bound to oxygen
    • C08K5/42Sulfonic acids; Derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L33/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • C08L33/04Homopolymers or copolymers of esters
    • C08L33/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L61/00Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
    • C08L61/20Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • C08L61/32Modified amine-aldehyde condensates
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L63/00Compositions of epoxy resins; Compositions of derivatives of epoxy resins
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/12All metal or with adjacent metals
    • Y10T428/12493Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
    • Y10T428/12535Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.] with additional, spatially distinct nonmetal component
    • Y10T428/12556Organic component
    • Y10T428/12569Synthetic resin
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/13Hollow or container type article [e.g., tube, vase, etc.]
    • Y10T428/1352Polymer or resin containing [i.e., natural or synthetic]
    • Y10T428/1355Elemental metal containing [e.g., substrate, foil, film, coating, etc.]
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/13Hollow or container type article [e.g., tube, vase, etc.]
    • Y10T428/1352Polymer or resin containing [i.e., natural or synthetic]
    • Y10T428/139Open-ended, self-supporting conduit, cylinder, or tube-type article
    • Y10T428/1393Multilayer [continuous layer]
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31511Of epoxy ether
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31511Of epoxy ether
    • Y10T428/31529Next to metal
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/3154Of fluorinated addition polymer from unsaturated monomers
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31678Of metal
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31855Of addition polymer from unsaturated monomers
    • Y10T428/31935Ester, halide or nitrile of addition polymer

Definitions

  • the invention relates to a one-step fluoropolymer, especially polyvinylidene fluoride (PVDF), coating for use on metals, especially use on metal fuel line and brake tubes, etc, to provide a protective barrier with superior chemical resistance, impact resistance and heat resistance as well as good flexibility.
  • the coating composition contains, on a resin solids basis, 75-94 percent polyvinylidene fluoride resin, 5-20 percent acrylic resin, and 1-15 percent polyepoxide resin.
  • the coating has excellent adhesion on metal substrates, particularly on non-pretreated galvanized steel, without the need for a primer coating.
  • Metal tubes such as brake tubes and metal fuel lines are required to have chemical resistance, salt spray corrosion resistance, impact resistance as well as heat resistance.
  • Protective coatings are generally applied to the metal which are capable of withstanding chemical erosion and mechanical erosion.
  • Fluorocarbon-based resins are known to provide excellent protection to metals, as, well as imparting a durable and aesthetic appearance. Unfortunately, the resins themselves adhere very poorly to metal substrates.
  • One method for increasing adhesion of a fluorocarbon-based coating to a metal is to apply a primer coating or other surface treatment, which improves the adhesion of the topcoat to the substrate and also improves the corrosion resistance of the substrate.
  • US 6,500,565 and US 2002/0090528 disclose a multilayer corrosion resistant PVDF coating for automobile brake tubes. The metal substrate is surface treated with a zinc or zinc- nickel plating layer and a cliromate film of trivalent chromium, and was primed with an epoxy layer.
  • US 4,379,885 discloses an acrylic based coating composition especially useful as a primer for metal substrates. The problem with these methods for providing a PVDF coating is that they involve two steps to ensure good adhesion of the PVDF film — an undercoating followed by the PVDF coating, which adds the expense and complexity of an added manufacturing step.
  • a one-step polyvinylidene coating for metal surfaces is described in US 5,130,201.
  • a maximum of 70% PVDF resin and a 7.5% minimum of a curing agent is exemplified.
  • the problem with the one-step coating of the '201 reference is that it sacrifices some of the protective properties of the coating by teaching lower levels of PVDF in the coating, and it also describes a highly cross-linked system with little flexibility, that can result in cracking of the coating.
  • a fluoropolymer coating having good adhesion, superior chemical resistance, impact resistance, corrosion resistance, abrasion resistance, heat resistance and good flexibility can be formed from a composition having greater than 75% fluoropolymer, 5-20% of an acrylic resin, 1-15% of a polyepoxide resin, and low level of crosslinking.
  • This coating provides the properties required for metal fuel lines and brake tubes.
  • An additional advantage is that brake tubes coated with the composition of the invention have excellent brake fluid resistance.
  • a composition comprising: s a) from 75 to 94 percent by weight of a fiuoropolymer resin; b) from 5 to 20 percent by weight of at least one acrylic resin; c) from 1 to 15 percent by weight of at least one epoxide resin; and d) optionally up to5 percent by weight of a crosslinker, all percentages based on a resins solids basis.
  • a process for coating a substrate comprising the steps of: forming the coating composition of the first objective; applying the coating composition to at least one surface of a substrate; and curing the coated surface at a temperature of at least 18O 0 C .
  • the invention relates to a one-step fiuoropolymer coating having a high level of a fiuoropolymer, which provides a flexible coating having excellent chemical, physical and heat resistance.
  • the coating composition of the invention contains from 75 to 94 weight percent of o one or more a fiuoropolymer resins, based on the total resin solids.
  • the coating contains from 80 to 90 percent of a fiuoropolymer, and most preferably from 82 to 88 percent fiuoropolymer.
  • fiuoropolymer resin any fiuoropolymer that is film-forming. These may be homopolymers, such as polyvinylidene fluoride, or copolymers, such as, but not limited to, vinylidene fluoride/ hexafluoropropylene copolymer, vinylidene fluoride/ chlorotetrafluoroethylene copolymer, vinylidene fluoride/tetrafluoroethylene copolymer 0 ethylene/tetrafluoroethylene copolymer, fluorinated ethylene propylene (FEP) and mixtures thereof. Fluoropolymers of the invention also include partially fluorinated polymers, such as ETFE and ECTFE, which may have similar decomposition products as fully fluorinated polymers.
  • ETFE and ECTFE partially fluorinated polymers
  • the fluoropolymer is a polyvinylidene fluoride polymer.
  • PVDF polyvinylidene fluoride polymer
  • PVDF resin or PVDF polymer refers not only to homopolymers of PVDF but also to copolymers prepared from at least about 75% by weight of vinylidene fluoride (VDF) 5 monomer.
  • Comonomers may include other fluorinated monomers such as: hexafluoropropylene (HFP), chlorotetrafluoroethylene (CTFE), tetrafluoroethylene (TFE), and vinyl fluoride.
  • the film forming fluoropolymer resin typically includes PVDF having a Mw of about 150,000 to about 450,000 and a melting point of about 150-170 0 C.
  • PVDF having a Mw of about 150,000 to about 450,000 and a melting point of about 150-170 0 C.
  • KYNAR ® 301F available form ARICEMA Inc.
  • the coating composition also contains from 5 to 20 weight percent, and preferably 5 to 15 percent, based on the total resin solids, of a thermoplastic acrylic.
  • the acrylic resin must be thermodynamically miscible with the fluoropolymer.
  • Useful acrylic resins include, but are not s limited to, polymers and copolymers made from methyl methacrylate, methyl acrylate, and ethyl acrylate monomers.
  • the acrylic resin is needed when the fluoropolymer is polyvinylidene fluoride in order to add some degree of functionality and therefore wetability and adhesion to the coating composition.
  • Other resins may also be used in the composition in small amounts, such as, for example, hydroxyl-functional polymer.
  • the coating composition also contains at least one polyepoxide resin.
  • the polyepoxide resin is any compound or mixture of compounds having a plurality of 1 ,2- epoxy groups.
  • the preferred polyepoxides have a molecular weight of from about 150 to about 5000.
  • a preferred class of polyepoxides are the polyglycidyl ethers of polyphenols.
  • EPON 1001 available form Resoution Performance Products.
  • Cycloaliphatic epoxy resins are also useful herein.
  • the epoxy resin is present at from 1 to 15 percent by weight, based on the total resin, and preferably from 2 to 10 percent by weight.
  • the coating adhesion will be negatively affected. If it is more than 15 weight percnt, the brake fluid o chemical resistance and coating flexibility will be negatively affected. It is also possible to use other polymers having functional groups and capable of forming crosslinks, with or instead of the polyepoxide, such as phenolic resins, organosilanes, and other known crosslink formers. Optionally a curing agent or crosslinking agent is also present in the coating composition. The curing agent is needed for the coating composition to have good brake fluid resistance, when the polyepoxide resin is used at more than 3 weight percent.
  • the curing agent is present at from 20 to 30 weight percent based on the epoxy resin weight, and 5 preferably about 25 percent by weight; or 0.2 to 5 percent by weight based on the total resin solids.
  • the curing agent is not required when polyepoxide resin is in the range of 1 to 3 weight percent on total resin.
  • Curing agents useful in the present invention include, but are not limited to melamine, isocyanate, blocked isocyanate, phenol resin, amino resin, and other known curing agents.
  • catalysts may also be added to accelerate the speed of the o reaction of the curing agent. The particular catalysts which are effective for different curing agents are known in the art.
  • the coating composition may contain other adjuncts as known in the art.
  • the adjuncts include, but are not limited to, pigments, dyes, fillers, anti-settling agents, leveling agents, surfactants, dispersing agents, and thickeners.
  • the coating composition of the present invention may be prepared by conventional methods. For example, the coating composition may be prepared by blending the various components using a disperser and milling equipment such as a small media mill or paint shaker.
  • the coating composition may be used as a powder, dissolved in a solvent to form a o solution, or dispersed in a solvent or combination of solvents to form a solvent dispersion.
  • Suitable solvents useful as a carrier for solvent dispersions are those which do not dissolve or swell PVDF at room temperature, but will solvate PVDF at elevated temperatures.
  • Suitable solvents include, but are not limited to, the higher ketones such as isophorone, methyl ethyl ketone, methyl isobutyl ketone, etc, glycol ethers such as dipropylene glycol methyl ether, 5 dipropylene glycol dimethyl ether, propylene glycol ⁇ -propyl ether, diethylene glycol butyl ether, etc, glycol ether esters such as diethylene glycol ethyl ether acetate, propylene glycol methyl ether acetate, etc., and other esters such as dimethyl phthalate and glyceryl triacetate.
  • the coating composition of the present invention may be used for coating metal substrates and other substrates exposed to the environment.
  • metals that can be o coated with the coating of the invention include, but are not limited to, iron, stainless steel, copper, aluminum, GALVALUME ® , ZINC ALUME ® , and both pretreated and non-pretreated galvanized steel.
  • metal substrates may be pretreated with an inorganic pretreatment, or primer, such as a hexavalent chromium pretreatment, a trivalent chromium pretreatment, an iron phosphate pretreatment, etc.
  • Other substrates that can benefit from being protected with the coating composition of the invention include substrates capable of withstanding the baking process, such as, but not limited to, ceramics, marble, glass, china, 5 and brick.
  • the substrate consists of brake tubes or metal fuel lines.
  • the coating composition may be applied to the substrate surface using a variety of well-known techniques such as spraying, brushing, electrostatic coating, dipping and roll coating.
  • the fluoropolymer film is then cured to form a coated substrate having an adhered polymer film.
  • the baking temperatures are not critical, but must be high enough to cause the fluoropolymer particles present in the dispersion to coalesce into a continuous film.
  • a temperature of at least about 18O 0 C for about 10 minutes is generally adequate for spray coatings based on vinylidene difluoride homopolymers.
  • the oven dwell temperature is often no more than about 50 seconds and oven temperatures as high as 35O 0 C may be used. 5
  • Vinylidene difluoride-based films are preferably cured by baking for a well time of about 30 —
  • Substrates coated with the composition of the invention have good adhesion on the substrates, superior chemical resistance, impact resistance, corrosion resistance, abrasion resistance, heat resistance and good flexibility. 0
  • PVDF Polyvinylidene Fluoride, available from Arkemalnc. as KYNAR® 30 IF PVDF.
  • PARALOID Acrylic B44 Methyl methacrylate-ethyl acrylate copolymer, available from
  • CYMEL 303 a modified melamine-formaldehyde resin, available from Cytec Industries Inc.
  • NACURE 2500 a p -Toluenesulfonic acid catalyst, available from King Industrues
  • Paint viscosity was tested using a 4 DIN viscosity cup. Color was read using a 5 HunterLab Labscan II; Geometry 0/45. The color reading is CIE L*a*b*, 10 degree observer, D65 illuminant. Gloss was read using a HunterLab ProGloss 3 (Geometry 85°). Flexibility (T-Bend formability) was measured according to ASTM D 4145 - 83 Standard Test Method for Coating Flexibility of Prepainted Sheet. Impact resistance was measured according to ASTM D 2794-90 Standard Test Method for Resistance of Organic Coatings to o the Effects of Rapid Deformation (Impact). If there is no cracking and it keeps 100% adhesion at 4.5mm deformation, it passes. Otherwise, it fails.
  • Brake fluid (DOT 3) and gasoline chemical resistance test place brake fluid or gasoline 5 drops on coating surface and cover it with a watch glass for 72hrs at room temperature.
  • the pencil hardness (ASTM D3363 -92a) before and after was measured. If there is no change in pencil hardness, it passes.
  • Articles coated with this compositions have superior impact resistance, chemical resistance, flexibility and heat resistance as well.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Paints Or Removers (AREA)
  • Laminated Bodies (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)

Abstract

The invention relates to a one-step fluoropolymer, especially polyvinylidene fluoride (PVDF), coating for use on metals, especially use on metal fuel line and brake tubes, etc, to provide a protective barrier with superior chemical resistance, impact resistance and heat resistance as well as good flexibility. The coating composition contains, on a resin solids basis, 75-94 percent polyvinylidene fluoride resin, 5-20 percent acrylic resin, and 1-15 percent polyepoxide polyepoxide resin. The coating has excellent adhesion on metal substrates, particularly on non-pretreated galvanized steel, without the need for a primer coating.

Description

POLYVINYLIDENE FLUORIDE COATING FOR METAL SUBSTRATES
Field of the Invention
The invention relates to a one-step fluoropolymer, especially polyvinylidene fluoride (PVDF), coating for use on metals, especially use on metal fuel line and brake tubes, etc, to provide a protective barrier with superior chemical resistance, impact resistance and heat resistance as well as good flexibility. The coating composition contains, on a resin solids basis, 75-94 percent polyvinylidene fluoride resin, 5-20 percent acrylic resin, and 1-15 percent polyepoxide resin. The coating has excellent adhesion on metal substrates, particularly on non-pretreated galvanized steel, without the need for a primer coating.
Background of the Invention
Metal tubes such as brake tubes and metal fuel lines are required to have chemical resistance, salt spray corrosion resistance, impact resistance as well as heat resistance. Protective coatings are generally applied to the metal which are capable of withstanding chemical erosion and mechanical erosion.
Fluorocarbon-based resins are known to provide excellent protection to metals, as, well as imparting a durable and aesthetic appearance. Unfortunately, the resins themselves adhere very poorly to metal substrates.
One method for increasing adhesion of a fluorocarbon-based coating to a metal is to apply a primer coating or other surface treatment, which improves the adhesion of the topcoat to the substrate and also improves the corrosion resistance of the substrate. US 6,500,565 and US 2002/0090528 disclose a multilayer corrosion resistant PVDF coating for automobile brake tubes. The metal substrate is surface treated with a zinc or zinc- nickel plating layer and a cliromate film of trivalent chromium, and was primed with an epoxy layer. US 4,379,885 discloses an acrylic based coating composition especially useful as a primer for metal substrates. The problem with these methods for providing a PVDF coating is that they involve two steps to ensure good adhesion of the PVDF film — an undercoating followed by the PVDF coating, which adds the expense and complexity of an added manufacturing step.
A one-step polyvinylidene coating for metal surfaces is described in US 5,130,201. A very wide range (10 to 95 %) of vinylidene fluoride and a very wide range (1 to 80%) of a poorly compatible resin, such as an epoxy resin, is described. A maximum of 70% PVDF resin and a 7.5% minimum of a curing agent is exemplified.
The problem with the one-step coating of the '201 reference is that it sacrifices some of the protective properties of the coating by teaching lower levels of PVDF in the coating, and it also describes a highly cross-linked system with little flexibility, that can result in cracking of the coating.
There is a need for a one-step coating having good adhesion, excellent chemical resistance such as brake fluid resistance, excellent protective properties, and flexibility for coating metal substrates, especially in applications such as for metal fuel lines and brake tubes.
Surprisingly it has been found that a fluoropolymer coating having good adhesion, superior chemical resistance, impact resistance, corrosion resistance, abrasion resistance, heat resistance and good flexibility, can be formed from a composition having greater than 75% fluoropolymer, 5-20% of an acrylic resin, 1-15% of a polyepoxide resin, and low level of crosslinking. This coating provides the properties required for metal fuel lines and brake tubes. An additional advantage is that brake tubes coated with the composition of the invention have excellent brake fluid resistance.
Summary of the Invention It is accordingly a first objective of the invention to produce a fluoropolymer coating having good adhesion to metal substrates.
It is a second objective of the invention to produce a fluoropolymer coating having a high level of fluoropolymer, for excellent chemical, impact, corrosion, abrasion and heat resistance. It is a third objective of the invention to produce a fluoropolymer composition that provides a flexible coating for use in metal fuel lines and brake tubes. It is a forth objective to produce a coated substrate, coated with a fluoropolymer composition by a one-step process.
These objectives of the invention are accomplished, in accordance with the principles of a preferred embodiment of the invention, by a composition comprising: s a) from 75 to 94 percent by weight of a fiuoropolymer resin; b) from 5 to 20 percent by weight of at least one acrylic resin; c) from 1 to 15 percent by weight of at least one epoxide resin; and d) optionally up to5 percent by weight of a crosslinker, all percentages based on a resins solids basis. o The objectives are further accomplished by a process for coating a substrate comprising the steps of: forming the coating composition of the first objective; applying the coating composition to at least one surface of a substrate; and curing the coated surface at a temperature of at least 18O0C .
5 Detailed description of the invention
The invention relates to a one-step fiuoropolymer coating having a high level of a fiuoropolymer, which provides a flexible coating having excellent chemical, physical and heat resistance.
The coating composition of the invention contains from 75 to 94 weight percent of o one or more a fiuoropolymer resins, based on the total resin solids. Preferably the coating contains from 80 to 90 percent of a fiuoropolymer, and most preferably from 82 to 88 percent fiuoropolymer.
It was found that lower levels of fiuoropolymer resins produced a coating having poorer chemical resistance. Higher levels of fiuoropolymer resins have an adverse effect 5 on adhesion to metal substrates.
By "fiuoropolymer resin" is meant any fiuoropolymer that is film-forming. These may be homopolymers, such as polyvinylidene fluoride, or copolymers, such as, but not limited to, vinylidene fluoride/ hexafluoropropylene copolymer, vinylidene fluoride/ chlorotetrafluoroethylene copolymer, vinylidene fluoride/tetrafluoroethylene copolymer 0 ethylene/tetrafluoroethylene copolymer, fluorinated ethylene propylene (FEP) and mixtures thereof. Fluoropolymers of the invention also include partially fluorinated polymers, such as ETFE and ECTFE, which may have similar decomposition products as fully fluorinated polymers.
Preferably the fluoropolymer is a polyvinylidene fluoride polymer. "PVDF" or PVDF resin or PVDF polymer refers not only to homopolymers of PVDF but also to copolymers prepared from at least about 75% by weight of vinylidene fluoride (VDF) 5 monomer. Comonomers may include other fluorinated monomers such as: hexafluoropropylene (HFP), chlorotetrafluoroethylene (CTFE), tetrafluoroethylene (TFE), and vinyl fluoride.
The film forming fluoropolymer resin typically includes PVDF having a Mw of about 150,000 to about 450,000 and a melting point of about 150-1700C. One example of a o commercially available PVDF, which is particularly suitable for use in the present composition, is KYNAR® 301F (available form ARICEMA Inc.).
The coating composition also contains from 5 to 20 weight percent, and preferably 5 to 15 percent, based on the total resin solids, of a thermoplastic acrylic. The acrylic resin must be thermodynamically miscible with the fluoropolymer. Useful acrylic resins include, but are not s limited to, polymers and copolymers made from methyl methacrylate, methyl acrylate, and ethyl acrylate monomers. The acrylic resin is needed when the fluoropolymer is polyvinylidene fluoride in order to add some degree of functionality and therefore wetability and adhesion to the coating composition. Other resins may also be used in the composition in small amounts, such as, for example, hydroxyl-functional polymer. o The coating composition also contains at least one polyepoxide resin. The polyepoxide resin is any compound or mixture of compounds having a plurality of 1 ,2- epoxy groups. The preferred polyepoxides have a molecular weight of from about 150 to about 5000. A preferred class of polyepoxides are the polyglycidyl ethers of polyphenols. One example of a commercially available polyepoxide resin, which is particularly suitable 5 for use in the present composition, is EPON 1001 (available form Resoution Performance Products). Cycloaliphatic epoxy resins are also useful herein. The epoxy resin is present at from 1 to 15 percent by weight, based on the total resin, and preferably from 2 to 10 percent by weight. If the epoxy resin content is less than 1 percent by weight, the coating adhesion will be negatively affected. If it is more than 15 weight percnt, the brake fluid o chemical resistance and coating flexibility will be negatively affected. It is also possible to use other polymers having functional groups and capable of forming crosslinks, with or instead of the polyepoxide, such as phenolic resins, organosilanes, and other known crosslink formers. Optionally a curing agent or crosslinking agent is also present in the coating composition. The curing agent is needed for the coating composition to have good brake fluid resistance, when the polyepoxide resin is used at more than 3 weight percent. The curing agent is present at from 20 to 30 weight percent based on the epoxy resin weight, and 5 preferably about 25 percent by weight; or 0.2 to 5 percent by weight based on the total resin solids. The curing agent is not required when polyepoxide resin is in the range of 1 to 3 weight percent on total resin. Curing agents useful in the present invention include, but are not limited to melamine, isocyanate, blocked isocyanate, phenol resin, amino resin, and other known curing agents. Optionally, catalysts may also be added to accelerate the speed of the o reaction of the curing agent. The particular catalysts which are effective for different curing agents are known in the art.
The coating composition may contain other adjuncts as known in the art. The adjuncts include, but are not limited to, pigments, dyes, fillers, anti-settling agents, leveling agents, surfactants, dispersing agents, and thickeners. 5 The coating composition of the present invention may be prepared by conventional methods. For example, the coating composition may be prepared by blending the various components using a disperser and milling equipment such as a small media mill or paint shaker.
The coating composition may be used as a powder, dissolved in a solvent to form a o solution, or dispersed in a solvent or combination of solvents to form a solvent dispersion.
Suitable solvents useful as a carrier for solvent dispersions are those which do not dissolve or swell PVDF at room temperature, but will solvate PVDF at elevated temperatures. Suitable solvents include, but are not limited to, the higher ketones such as isophorone, methyl ethyl ketone, methyl isobutyl ketone, etc, glycol ethers such as dipropylene glycol methyl ether, 5 dipropylene glycol dimethyl ether, propylene glycol π-propyl ether, diethylene glycol butyl ether, etc, glycol ether esters such as diethylene glycol ethyl ether acetate, propylene glycol methyl ether acetate, etc., and other esters such as dimethyl phthalate and glyceryl triacetate.
The coating composition of the present invention may be used for coating metal substrates and other substrates exposed to the environment. Examples of metals that can be o coated with the coating of the invention include, but are not limited to, iron, stainless steel, copper, aluminum, GALVALUME®, ZINC ALUME®, and both pretreated and non-pretreated galvanized steel. Optionally, metal substrates may be pretreated with an inorganic pretreatment, or primer, such as a hexavalent chromium pretreatment, a trivalent chromium pretreatment, an iron phosphate pretreatment, etc. Other substrates that can benefit from being protected with the coating composition of the invention include substrates capable of withstanding the baking process, such as, but not limited to, ceramics, marble, glass, china, 5 and brick.
In one embodiment the substrate consists of brake tubes or metal fuel lines. The coating composition may be applied to the substrate surface using a variety of well-known techniques such as spraying, brushing, electrostatic coating, dipping and roll coating. The fluoropolymer film is then cured to form a coated substrate having an adhered polymer film. o The baking temperatures are not critical, but must be high enough to cause the fluoropolymer particles present in the dispersion to coalesce into a continuous film. A temperature of at least about 18O0C for about 10 minutes is generally adequate for spray coatings based on vinylidene difluoride homopolymers. In roll or dipping coating processes, the oven dwell temperature is often no more than about 50 seconds and oven temperatures as high as 35O0C may be used. 5 Vinylidene difluoride-based films are preferably cured by baking for a well time of about 30 —
60 seconds such that the metal substrate reaches a peak metal temperature of 2250C to 26O0C.
Substrates coated with the composition of the invention have good adhesion on the substrates, superior chemical resistance, impact resistance, corrosion resistance, abrasion resistance, heat resistance and good flexibility. 0
Examples
The following examples are intended to illustrate further various aspects of the present invention, but are not intended to limit the scope of the invention in any aspect.
5 Raw materials:
PVDF: Polyvinylidene Fluoride, available from Arkemalnc. as KYNAR® 30 IF PVDF. PARALOID Acrylic B44: Methyl methacrylate-ethyl acrylate copolymer, available from
Rohm and Haas, supplied as a 40 wt% solution in toluene EPON 1001 : a Bisphenol A-based epoxy resin, available from Resolution Performance o Products, supplied as a 75 wt% solution in toluene.
CYMEL 303 : a modified melamine-formaldehyde resin, available from Cytec Industries Inc. NACURE 2500: a p -Toluenesulfonic acid catalyst, available from King Industrues
Test Method:
Paint viscosity was tested using a 4 DIN viscosity cup. Color was read using a 5 HunterLab Labscan II; Geometry 0/45. The color reading is CIE L*a*b*, 10 degree observer, D65 illuminant. Gloss was read using a HunterLab ProGloss 3 (Geometry 85°). Flexibility (T-Bend formability) was measured according to ASTM D 4145 - 83 Standard Test Method for Coating Flexibility of Prepainted Sheet. Impact resistance was measured according to ASTM D 2794-90 Standard Test Method for Resistance of Organic Coatings to o the Effects of Rapid Deformation (Impact). If there is no cracking and it keeps 100% adhesion at 4.5mm deformation, it passes. Otherwise, it fails. The pencil test is done with a Turquoise pencil according to ASTM D 3363 -92a "Standard Test Method for Film Hardness by Pencil Test", brand. The surface hardness is defined by the hardest pencil grade that fails to scratch the film. s Cross hatch adhesion (ASTM D 3359 - 90) was tested using Gardco Paint Adhesion
Test Kit. 0-5 grade (worst to best) was used to compare the adhesion. 5 is 100% adhesion pass. 4 is more than 90% but less than 100% adhesion pass. 3 is more than 60% but less than 90% adhesion pass. 2 is more than 30% but less than 60% adhesion pass. 1 is more than 0 but less than 30% adhesion pass. 0 is 0% adhesion pass. o Thermal stability: coating samples were placed in oven at 150°C for 24 hours. The color and pencil hardness (ASTM D3363 -92a) before and after the heating were measured. If color change CIELAB ΔE* < 5 and if there is not a decrease in pencil hardness, it passes. Otherwise, it fails.
Brake fluid (DOT 3) and gasoline chemical resistance test: place brake fluid or gasoline 5 drops on coating surface and cover it with a watch glass for 72hrs at room temperature. The pencil hardness (ASTM D3363 -92a) before and after was measured. If there is no change in pencil hardness, it passes.
Working Example 1-6 and Comparative Example 1-7 o The ingredients in Table 1 below were blended and shaken 1 hour on a paint shaker. The resulting paints were then cast on both chromated (Cr+6) aluminum AA3003 panels and non- pretreated galvanized steel substrates using wire- wrapped draw down rods (#52). The steel tube samples were made using brush coating. The resulting films, tubes and panels were baked at 585°F for 50 seconds and then quenched with cold water. Films were then tested for physical and mechanical properties, with the results in Table 2.
TABLE 1
Figure imgf000009_0001
TABLE 2
Figure imgf000009_0002
* 5: 100% adhesion pass; 4: 90%< adhesion < 100%; 3: 60%< adhesion < 90%; 2: 30% < adhesion < 60%; 1 : 0% < adhesion < 30%; 0: 0% adhesion.
5 As seen from the results of working examples and comparative examples, the incorporation of a small amount of polyepoxide co-resin brought in a significant improvement in adhesion, particularly on non-pretreated galvanized steel (working examples 1-6 vs comparative example 1). Higher level of polyepoxide resin might result in a poorer brake fluid resistance. However, a much better brake fluid resistance could be achieved by using a melamine i o crosslinker (working examples 2-4 vs comparative examples 2-4). However, when the PVDF content is lower than 75%, even with the use of melamine crosslinker agent, the brake fluid resistance is not good (comparative examples 5,6 & 7). Using a blend of PVDF (75-90%), acrylic (5-20%) and polyepoxide resin (1-15%) with melamine crosslinker, the formulations have a very good adhesion on both chromated aluminum and non-pretreated galvanized steel
15 substrates. Articles coated with this compositions have superior impact resistance, chemical resistance, flexibility and heat resistance as well.

Claims

What is claimed is
1. A coating composition for metal substrates comprising: a) from 75 to 94 percent by weight of at least one fluoropolymer resin; b) from 5 to 20 percent by weight of at least one acrylic resin; c) from 1 to 15 percent by weight of at least one epoxide resin; and d) optionally up to 5 percent by weight of at least one curing agent, all percentages based on a resins solids basis, with the total adding to 100 percent.
2. The coating composition of claim 1 wherein said fluoropolymer resin comprises a polyvinylidene fluoride homopolymer or copolymer having at least 75 percent by weight of vinylidene fluoride monomer units.
3. The coating composition of claim 1 comprising from 80 to 90 percent by weight of at least one fluoropolymer resin.
4. The coating composition of claim 3 comprising from 82 to 88 percent by weight of at least one fluoropolymer resin.
5. The coating composition of claim 1 comprising from 5 to 15 percent by weight of at least one acrylic resin.
6. The coating composition of claim 1 comprising from 2 to 10 percent by weight of at least one epoxide resin.
7. The coating composition of claim 1 comprising from 3 to 15 percent by weight of at least one epoxide resin and further comprising from 0.2 to 5 percent by weight of a curing agent.
8. The coating composition of claim 1 wherein said curing agent comprises a melamine.
9. A process for providing a flexible, chemical and physical resistant on a substrate comprising the steps of: a) forming the coating composition of claim 1 ; b) applying the coating composition to at least one surface of a substrate; and a) curing the coated surface at a temperature of at least 18O0C .
10. A coated substrate comprising: a) a substrate capable of retaining its shape at a temperature of at least 18O0C ; and b) a coating composition directly deposited on at least one surface of the substrate, wherein said coating composition comprises
( 1 ) from 75 to 94 percent by weight of at least one fluoropolymer resin;
( 2 ) from 5 to 20 percent by weight of at least one acrylic resin;
( 3 ) from 1 to 15 percent by weight of at least one epoxide resin; and
( 4 ) optionally up to 5 percent by weight of a curing agent, all percentages based on a resins solids basis, with the total adding to 100 percent.
11. The coated substrate of claim 10, wherein said substrate comprises a metal, ceramic, marble, glass, china, or brick substrate.
12. The coated substrate of claim 11, wherein said metal substrate is selected from iron, stainless steel, copper, aluminum, and pretreated and non-pretreated galvanized steel.
13. The coated substrate of claim 12, wherein said coated substrate comprises a metal fuel line or brake tube.
PCT/US2005/047118 2005-01-21 2005-12-27 Polyvinylidene fluoride coating for metal substrates Ceased WO2006078425A2 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
EP20050855641 EP1838529A2 (en) 2005-01-21 2005-12-27 Polyvinylidene fluoride coating for metal substrates
JP2007552144A JP2008528727A (en) 2005-01-21 2005-12-27 Polyvinylidene fluoride coating for metal substrates

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US11/039,979 US7399533B2 (en) 2005-01-21 2005-01-21 Polyvinylidene fluoride coating for metal substrates
US11/039,979 2005-01-21

Publications (2)

Publication Number Publication Date
WO2006078425A2 true WO2006078425A2 (en) 2006-07-27
WO2006078425A3 WO2006078425A3 (en) 2009-04-02

Family

ID=36692700

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2005/047118 Ceased WO2006078425A2 (en) 2005-01-21 2005-12-27 Polyvinylidene fluoride coating for metal substrates

Country Status (5)

Country Link
US (1) US7399533B2 (en)
EP (1) EP1838529A2 (en)
JP (1) JP2008528727A (en)
CN (1) CN101443194A (en)
WO (1) WO2006078425A2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2115012A4 (en) * 2007-01-26 2010-08-25 Greene Tweed Inc METHOD FOR FIXING PERFLUOROELASTOMERIC MATERIALS TO A SURFACE
JP2011500372A (en) * 2007-10-18 2011-01-06 アーケマ・インコーポレイテッド Colored multilayer composition with high solar reflectance
CN102286242A (en) * 2011-07-15 2011-12-21 苏州吉人漆业有限公司 Acrylic polyurethane hot galvanizing substrate paint and preparation method thereof
US11827778B2 (en) 2017-06-15 2023-11-28 Arkema France Ink based on fluorinated polymer having improved adhesion

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4446450B2 (en) * 2004-03-29 2010-04-07 日産自動車株式会社 Automotive sliding device
US20050229992A1 (en) * 2004-04-06 2005-10-20 Mckeen Laurence W Lined vessels for conveying chemicals
CA2719795A1 (en) * 2008-03-27 2009-10-01 Greene, Tweed Of Delaware, Inc. Inert substrate-bonded fluoroelastomer components and related methods
EP3517585B1 (en) 2011-03-08 2021-06-30 Swimc, LLC Method for coating a cargo container
JP6162601B2 (en) * 2011-06-30 2017-07-12 東洋鋼鈑株式会社 Fuel pipe
US8727069B1 (en) 2012-12-05 2014-05-20 United Technologies Corporation Oscillating tube having a segmented coating for damping the tube
CN104448985A (en) * 2013-11-30 2015-03-25 东莞市长安东阳光铝业研发有限公司 Application of a kind of acrylic acid prepolymer in polyvinylidene fluoride coil coating
US9385374B2 (en) * 2014-04-01 2016-07-05 Ppg Industries Ohio, Inc. Electrode binder composition for lithium ion electrical storage devices
AU2015284559A1 (en) 2014-07-01 2017-01-12 Arkema Inc. Stable aqueous fluoropolymer coating composition
CN108160427A (en) * 2017-12-29 2018-06-15 重庆全茂合渝科技有限公司 A kind of motorcycle accessories surface even application technique
JP7102766B2 (en) * 2018-02-19 2022-07-20 日本製鉄株式会社 Painted metal plate
KR20240138130A (en) 2018-09-19 2024-09-20 허니웰 인터내셔날 인코포레이티드 Fluorocopolymers for coating applications

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3324069A (en) 1964-10-23 1967-06-06 Pennsalt Chemicals Corp Vinylidene fluoride polymer dispersions
US4379885A (en) 1980-12-29 1983-04-12 Ppg Industries, Inc. Fluorocarbon coating compositions
US4356284A (en) 1981-10-29 1982-10-26 Automation Industries, Inc. Thermoplastic compositions containing polyvinylidene fluoride and chlorinated polyethylene
US4659768A (en) 1986-02-03 1987-04-21 Desoto, Inc. Thermosetting fluorocarbon polymer coatings
US4684677A (en) 1986-02-13 1987-08-04 Desoto, Inc. Thermosetting fluorocarbon polymer primers
JP2581077B2 (en) 1987-06-09 1997-02-12 ダイキン工業株式会社 Vinylidene fluoride resin composition
US6500565B2 (en) 1994-08-30 2002-12-31 Usui Kokusai Sangyo Kaisha Limited Corrosion resistant resin coating structure in a metal tube
JP2003194288A (en) 2001-12-26 2003-07-09 Maruyasu Industries Co Ltd Metallic pipe surface treatment structure and surface treatment method

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2115012A4 (en) * 2007-01-26 2010-08-25 Greene Tweed Inc METHOD FOR FIXING PERFLUOROELASTOMERIC MATERIALS TO A SURFACE
EP2617738A1 (en) * 2007-01-26 2013-07-24 Greene, Tweed Of Delaware, Inc. Method of bonding perfluoroelastomeric materials to a surface
EP3461849A1 (en) * 2007-01-26 2019-04-03 Greene, Tweed Technologies, Inc. Method of bonding perfluoroelastomeric materials to a surface
US10961369B2 (en) 2007-01-26 2021-03-30 Green, Tweed Technologies Method of bonding perfluoroelastomeric materials to a surface
US11390726B2 (en) 2007-01-26 2022-07-19 Greene, Tweed Technologies, Inc. Method of bonding perfluoroelastomeric materials to a surface
JP2011500372A (en) * 2007-10-18 2011-01-06 アーケマ・インコーポレイテッド Colored multilayer composition with high solar reflectance
CN102286242A (en) * 2011-07-15 2011-12-21 苏州吉人漆业有限公司 Acrylic polyurethane hot galvanizing substrate paint and preparation method thereof
US11827778B2 (en) 2017-06-15 2023-11-28 Arkema France Ink based on fluorinated polymer having improved adhesion

Also Published As

Publication number Publication date
US20060166004A1 (en) 2006-07-27
JP2008528727A (en) 2008-07-31
EP1838529A2 (en) 2007-10-03
US7399533B2 (en) 2008-07-15
WO2006078425A3 (en) 2009-04-02
CN101443194A (en) 2009-05-27

Similar Documents

Publication Publication Date Title
US7399533B2 (en) Polyvinylidene fluoride coating for metal substrates
EP2922918B1 (en) A waterborne anticorrosion coating composition and process for providing a corrosion-resistant coating on a metal surface
JP2869443B2 (en) Top coating composition
US6017639A (en) Vinylidene difluoride-based coating compositions
JP2863076B2 (en) Curable resin composition, coating composition and coating film forming method
JPS6072965A (en) Low temperature curable coating composition
JPS62146965A (en) Flexible primer composition
JPH11300271A (en) Method for forming multilayer powder coating film
CN1625588A (en) No under coat anticorrosion composite without chromate and preparation method thereof
JP4766727B2 (en) COATING COMPOSITION AND COATED METAL PLATE USING THE COMPOSITION
JP2006219731A (en) Coating material composition for rear surface of precoated metal and precoated metal obtained by using the same
AU661246B2 (en) Isophorone-free fluorocarbon coating composition
JP3232153B2 (en) Manufacturing method of painted steel sheet
WO2004024835A1 (en) Self-priming chromate free corrosion resistant coating composition and method
JP4184561B2 (en) COATING COMPOSITION AND COATED METAL PLATE HAVING COATING FROM THE COMPOSITION
JP2000136321A (en) Primer for sealant
JP4119014B2 (en) Top coating composition and method for forming coating film thereof
EP3166983B1 (en) Curable film-forming compositions and method of mitigating dirt build-up on a substrate
JPH02245067A (en) Water-repellent coating composition
JP3288461B2 (en) Undercoat paint and method for producing coated steel sheet using the same
CA2225579A1 (en) Vehicles for paints and varnishes formulated with vinylidene fluoride-hexafluoropropylene copolymers
JP4292773B2 (en) Fluorine resin matte paint composition
JPH07228833A (en) Paint composition
JPH044080A (en) Production of coated film
EP0857769A1 (en) Vehicles for paints and varnishes formulated with vinylidene fluoride-hexafluoropropylene copolymers

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 200580046944.1

Country of ref document: CN

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: 2007552144

Country of ref document: JP

Ref document number: 2005855641

Country of ref document: EP

NENP Non-entry into the national phase

Ref country code: DE