WO2011040374A1 - 複層塗膜形成方法 - Google Patents

複層塗膜形成方法 Download PDF

Info

Publication number
WO2011040374A1
WO2011040374A1 PCT/JP2010/066713 JP2010066713W WO2011040374A1 WO 2011040374 A1 WO2011040374 A1 WO 2011040374A1 JP 2010066713 W JP2010066713 W JP 2010066713W WO 2011040374 A1 WO2011040374 A1 WO 2011040374A1
Authority
WO
WIPO (PCT)
Prior art keywords
coating film
resin
acid
parts
organic solvent
Prior art date
Application number
PCT/JP2010/066713
Other languages
English (en)
French (fr)
Japanese (ja)
Inventor
福田　徹
啓介 佐井
伶美 葛西
Original Assignee
関西ペイント株式会社
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 関西ペイント株式会社 filed Critical 関西ペイント株式会社
Priority to IN2722DEN2012 priority Critical patent/IN2012DN02722A/en
Priority to US13/498,880 priority patent/US8568833B2/en
Priority to JP2011534234A priority patent/JPWO2011040374A1/ja
Priority to CN2010800436576A priority patent/CN102548669A/zh
Publication of WO2011040374A1 publication Critical patent/WO2011040374A1/ja

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
    • B05D1/00—Processes for applying liquids or other fluent materials
    • B05D1/36—Successively applying liquids or other fluent materials, e.g. without intermediate treatment
    • 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
    • B05D7/56—Three layers or more
    • B05D7/57—Three layers or more the last layer being a clear coat
    • 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
    • B05D7/24—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 for applying particular liquids or other fluent materials
    • B05D7/26—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 for applying particular liquids or other fluent materials synthetic lacquers or varnishes
    • 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
    • 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
    • B05D7/56—Three layers or more
    • B05D7/57—Three layers or more the last layer being a clear coat
    • B05D7/572—Three layers or more the last layer being a clear coat all layers being cured or baked together
    • B05D7/5723—Three layers or more the last layer being a clear coat all layers being cured or baked together all layers being applied simultaneously
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D133/00—Coating 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 only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
    • C09D133/04—Homopolymers or copolymers of esters
    • C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C09D133/08—Homopolymers or copolymers of acrylic acid esters
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D133/00—Coating 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 only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
    • C09D133/04—Homopolymers or copolymers of esters
    • C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C09D133/10—Homopolymers or copolymers of methacrylic acid esters
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
    • C09D167/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
    • 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
    • B05D2202/00—Metallic substrate
    • B05D2202/10—Metallic substrate based on Fe
    • 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
    • B05D7/56—Three layers or more
    • B05D7/57—Three layers or more the last layer being a clear coat
    • B05D7/572—Three layers or more the last layer being a clear coat all layers being cured or baked together
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
    • C08L61/20—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • C08L61/26—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds
    • C08L61/28—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds with melamine
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31786—Of polyester [e.g., alkyd, etc.]
    • Y10T428/31797—Next to addition polymer from unsaturated monomers

Definitions

  • the present invention relates to a method for forming a multilayer coating film having excellent chipping resistance and appearance.
  • an electrodeposition coating film is formed on an object to be coated, and then an intermediate coating paint ⁇ baking cure ⁇ base coat paint coating ⁇ clear paint coating ⁇ baking cure 3 coat 2 bake ( 3C2B)
  • 3C2B 3 coat 2 bake
  • a method of forming a multi-layer coating film by a 3-coat 1-bake (3C1B) system is attempted (for example, coating of an intermediate coating, coating of a base coating, coating of a clear coating, and baking curing) (for example, Patent Document 1).
  • thermosetting intermediate coating material As a countermeasure, for example, in Patent Document 1, in the 3C1B system, as a thermosetting intermediate coating material, (A) a specific structural unit is contained in a specific amount, a hydroxyl value is 60 to 200 mgKOH / g, and a number average molecular weight is A vinyl copolymer having 2000 to 6000, (B) a polyester resin having a hydroxyl value of 80 to 120 mgKOH / g and a number average molecular weight of 1500 to 2600, (C) a non-aqueous polymer dispersion, (D ) When using a paint containing one or more cross-linkable resins selected from the group consisting of alkyl etherified melamine resins and blocked polyisocyanate resins, coating films such as appearance, chipping resistance, adhesion and weather resistance It is described that the performance does not decrease.
  • Patent Document 2 discloses that the 3C1B system is obtained by polycondensation of an acid component containing 80 mol% or more of isophthalic acid and a polyhydric alcohol as an intermediate coating, and has a glass transition point (Tg) of 40 to 40.
  • Isocyanate compound obtained by reacting hexamethylene diisocyanate and hexamethylene diisocyanate with a compound that reacts with hexamethylene diisocyanate and a compound having an active methylene group (c) 15 to 30% by weight, non-water having a core-shell structure
  • Desperation resin (d) 4-15 layers % (The amount of (a) to (d) is based on the weight of the solid content of the coating resin), and a flat pigment (e) having a major axis of 1 to 10 ⁇ m and a number average particle size of 2 to 6 ⁇ m. It is described that a multi-layer coating film excellent in finished appearance and chipping resistance can be formed when a paint containing 4 to 2 parts by weight (the solid content of the paint resin is 100 parts by weight) is used.
  • an object of the present invention is to provide a multilayer coating film forming method capable of forming a coating film excellent in smoothness and chipping resistance in the 3C1B system.
  • the inventors of the present invention as a first colored paint, in the coating process of the multilayer coating film by the 3C1B method, have a specific structure, a hydroxyl value, and a number average molecular weight.
  • an organic solvent-type paint containing a catalyst it has been found that a multilayer coating film excellent in smoothness and chipping resistance can be formed, and the present invention has been completed.
  • the present invention provides the following multilayer coating film forming method and an article on which a multilayer coating film is formed by the multilayer coating film forming method. 1.
  • the organic solvent-type first colored paint (A) contains (a1) 1.0 to 8.0 mol / kg (resin solid content) of a linear alkylene group having 4 or more carbon atoms in the molecule, A coating composition containing a
  • the organic solvent-type first colored paint (A) is 30 to 90 parts by mass of the hydroxyl group-containing polyester resin (a1) based on 100 parts by mass of the total solid content of the hydroxyl group-containing polyester resin (a1) and the melamine resin (a2). 4.
  • the organic solvent type second colored paint (B) is 30 to 95 parts by mass of the hydroxyl group-containing acrylic resin (b1) based on 100 parts by mass of the total solid content of the hydroxyl group-containing acrylic resin (b1) and the melamine resin (b2). 6.
  • a first colored paint, a second colored paint, and a clear paint are sequentially applied on an object to be coated, and the resulting three-layered multi-layered film is heated and cured simultaneously.
  • a multilayer coating film excellent in smoothness, chipping resistance and water resistance can be formed.
  • the second colored paint contains a glitter pigment
  • a multilayer coating film having an excellent appearance with high flip-flop properties and little metallic unevenness can be formed.
  • step (1) of the method for forming a multilayer coating film of the present invention (a1) 1.0 to 8.0 mol / kg of a linear alkylene group having 4 or more carbon atoms in the molecule is added to the object to be coated (resin A solid content), a hydroxyl group value within a range of 30 to 160 mg KOH / g, and a number average molecular weight within a range of 1,000 to 6,000, and (a2) a melamine resin An organic solvent type first colored paint (A) is applied to form an uncured first colored coating film.
  • the hydroxyl group-containing polyester resin (a1) contains 1.0 to 8.0 mol / kg (solid resin content) of a linear alkylene group having 4 or more carbon atoms in the molecule, and the hydroxyl value is within the range of 30 to 160 mgKOH / g. And a hydroxyl group-containing polyester resin having a number average molecular weight in the range of 1,000 to 6,000.
  • the hydroxyl group-containing polyester resin (a1) can be usually produced by an esterification reaction or an ester exchange reaction between an acid component (a1-1) and an alcohol component (a1-2).
  • the acid component (a1-1) a compound usually used as an acid component in the production of a polyester resin can be used.
  • the acid component (a1-1) include an aliphatic polybasic acid (a1-1-1), an alicyclic polybasic acid (a1-1-2), and an aromatic polybasic acid (a1-1-1-). 3) and the like.
  • the aliphatic polybasic acid (a1-1-1) is generally an aliphatic compound having two or more carboxyl groups in one molecule, an acid anhydride of the aliphatic compound, and an esterified product of the aliphatic compound. is there.
  • aliphatic polybasic acid (a1-1-1) examples include butanedioic acid (succinic acid), pentanedioic acid (glutaric acid), hexanedioic acid (adipic acid), heptanedioic acid (pimelic acid), Fats such as octanedioic acid (suberic acid), nonanedioic acid (azeleic acid), decanedioic acid (sebacic acid), undecanedioic acid, dodecanedioic acid, tridecanedioic acid (brassic acid), hexadecanedioic acid and octadecanedioic acid Aliphatic polycarboxylic acids; anhydrides of these aliphatic polycarboxylic acids; lower alkyl esterified products of these aliphatic polycarboxylic acids. These can be used alone or in combination of two or more.
  • the aliphatic polybasic acid (a1-1-1) is preferably 4 or more carbon atoms, more preferably 4 from the viewpoints of smoothness, sharpness, water resistance and chipping resistance of the resulting coating film.
  • Preferred examples include aliphatic dicarboxylic acids having 18 to 18 and more preferably 6 to 12 linear alkylene groups.
  • Examples of the aliphatic dicarboxylic acid having a linear alkylene group having 4 or more carbon atoms include hexanedioic acid (adipic acid), heptanedioic acid (pimelic acid), octanedioic acid (suberic acid), and nonanedioic acid (azeline).
  • decanedioic acid decanedioic acid (sebacic acid), undecanedioic acid, dodecanedioic acid, tridecanedioic acid (brassic acid), hexadecanedioic acid and octadecanedioic acid; anhydrides of these aliphatic dicarboxylic acids; Examples include lower alkyl esterified products. These can be used alone or in combination of two or more.
  • the alicyclic polybasic acid (a1-1-2) is generally a compound having one or more alicyclic structures (mainly 4 to 6 membered rings) and two or more carboxyl groups in one molecule, An acid anhydride of the compound and an esterified product of the compound.
  • Examples of the alicyclic polybasic acid (a1-1-2) include 1,2-cyclohexanedicarboxylic acid, 1,3-cyclohexanedicarboxylic acid, 1,4-cyclohexanedicarboxylic acid, and 4-cyclohexene-1,2.
  • Fats such as dicarboxylic acid, 3-methyl-1,2-cyclohexanedicarboxylic acid, 4-methyl-1,2-cyclohexanedicarboxylic acid, 1,2,4-cyclohexanetricarboxylic acid and 1,3,5-cyclohexanetricarboxylic acid
  • Examples thereof include cyclic polyvalent carboxylic acids; anhydrides of these alicyclic polyvalent carboxylic acids; and lower alkyl esterified products of these alicyclic polyvalent carboxylic acids. These can be used alone or in combination of two or more.
  • the aromatic polybasic acid (a1-1-3) is generally an aromatic compound having two or more carboxyl groups in one molecule, an acid anhydride of the aromatic compound, and an esterified product of the aromatic compound. is there.
  • aromatic polybasic acid (a1-1-3) examples include aromatics such as phthalic acid, isophthalic acid, terephthalic acid, naphthalenedicarboxylic acid, 4,4′-biphenyldicarboxylic acid, trimellitic acid, and pyromellitic acid.
  • aromatic polybasic acid phthalic acid, phthalic anhydride, isophthalic acid, trimellitic acid and trimellitic anhydride are particularly preferable.
  • an acid component (a1-1) other than the aliphatic polybasic acid (a1-1-1), the alicyclic polybasic acid (a1-1-2) and the aromatic polybasic acid (a1-1-3) For example, coconut oil fatty acid, cottonseed oil fatty acid, hemp seed oil fatty acid, rice bran oil fatty acid, fish oil fatty acid, tall oil fatty acid, soybean oil fatty acid, linseed oil fatty acid, tung oil fatty acid, rapeseed oil fatty acid, castor oil fatty acid, dehydrated castor oil fatty acid and Fatty acids such as safflower oil fatty acids; such as lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, linoleic acid, linolenic acid, benzoic acid, p-tert-butylbenzoic acid, cyclohexane acid and 10-phenyloctadecanoic acid Monocarboxylic acid; hydroxy
  • a polyhydric alcohol having two or more hydroxyl groups in one molecule can be preferably used.
  • polyhydric alcohol examples include aliphatic diol (a1-2-1), alicyclic diol (a1-2-2), and aromatic diol (a1-2-3).
  • the aliphatic diol (a1-2-1) is generally an aliphatic compound having two hydroxyl groups in one molecule.
  • Examples of the aliphatic diol (a1-2-1) include ethylene glycol, propylene glycol, diethylene glycol, trimethylene glycol, tetraethylene glycol, triethylene glycol, dipropylene glycol, 1,4-butanediol, 1,3 -Butanediol, 2,3-butanediol, 1,2-butanediol, 3-methyl-1,2-butanediol, 2-butyl-2-ethyl-1,3-propanediol, 1,2-pentanediol 1,5-pentanediol, 1,4-pentanediol, 2,4-pentanediol, 2,3-dimethyltrimethylene glycol, tetramethylene glycol, 3-methyl-4,3-pentanediol, 3-methyl- 1,5-pentanediol, 2,2,4-trimethyl 1,3-pentanediol, 1,6-hex
  • the aliphatic diol (a1-2-1) is preferably 4 or more carbon atoms, more preferably 4 to 12 carbon atoms, and still more preferably from the viewpoints of smoothness, sharpness, chipping resistance, and the like of the resulting coating film.
  • Preferable are aliphatic diols having 6 to 10 linear alkylene groups.
  • Examples of the aliphatic diol having a linear alkylene group having 4 or more carbon atoms include 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, 1,7-heptanediol, 1, Examples include 8-octanediol and 1,9-nonanediol. These can be used alone or in combination of two or more.
  • the alicyclic diol (a1-2-2) is generally a compound having one or more alicyclic structures (mainly 4- to 6-membered rings) and two hydroxyl groups in one molecule.
  • Examples of the alicyclic diol (a1-2-2) include dihydric alcohols such as 1,4-cyclohexanedimethanol, tricyclodecane dimethanol, hydrogenated bisphenol A, and hydrogenated bisphenol F; Examples include polylactone diols obtained by adding lactones such as ⁇ -caprolactone to alcohol. These can be used alone or in combination of two or more.
  • the aromatic diol (a1-2-3) is generally an aromatic compound having two hydroxyl groups in one molecule.
  • aromatic diol (a1-2-3) examples include ester diols such as bis (hydroxyethyl) terephthalate; alkylene oxide adducts of bisphenol A, and the like. These can be used alone or in combination of two or more.
  • polyhydric alcohol other than the aliphatic diol (a1-2-1), alicyclic diol (a1-2-2) and aromatic diol (a1-2-3) include, for example, polyethylene glycol, polypropylene glycol, and Polyether diols such as polybutylene glycol; glycerin, trimethylolethane, trimethylolpropane, diglycerin, triglycerin, 1,2,6-hexanetriol, pentaerythritol, dipentaerythritol, tris (2-hydroxyethyl) isocyania Trihydric or higher alcohols such as nurate, sorbitol, and mannitol; and polylactone polyols obtained by adding lactones such as ⁇ -caprolactone to these trihydric or higher alcohols.
  • Examples of the alcohol component (a1-2) other than the polyhydric alcohol include monoalcohols such as methanol, ethanol, propyl alcohol, butyl alcohol, stearyl alcohol, and 2-phenoxyethanol; propylene oxide, butylene oxide, and synthetic hyperbranches.
  • Examples thereof include alcohol compounds obtained by reacting monoepoxy compounds such as glycidyl esters of saturated fatty acids (trade name “Cardura E10”, manufactured by HEXION Specialty Chemicals) and acids.
  • Hydroxyl-containing polyester resin (a1) The content of linear alkylene groups having 4 or more carbon atoms in the molecule is 1.0 to 8.0 mol / kg (resin solid content), more preferably 2 to 7 mol / kg. More preferably, it is ⁇ 6 mol / kg mol / kg.
  • the straight-chain alkylene group has 4 or more carbon atoms.
  • it is preferably in the range of 4 to 12, and in the range of 6 to 10. More preferably it is.
  • Examples of the hydroxyl group-containing polyester resin containing a linear alkylene group having 4 or more carbon atoms in the molecule include, as an acid component (a1-1), an aliphatic dicarboxylic acid having the linear alkylene group having 4 or more carbon atoms. Or an aliphatic diol having a linear alkylene group having 4 or more carbon atoms as the alcohol component (a1-2).
  • the “content of linear alkylene group having 4 or more carbon atoms” in the hydroxyl group-containing polyester resin (a1) molecule is the number of carbon atoms contained in 1 kg (solid content) of the hydroxyl group-containing polyester resin (a1). It is the number of moles of a linear alkylene group of 4 or more. This is because the total number of moles (Wm) of the monomer having a linear alkylene group having 4 or more carbon atoms contained in the monomer used for the synthesis of the hydroxyl group-containing polyester resin (a1) is the resin mass (Wr) excluding the condensed water. : Unit kg) and can be calculated by dividing (ie, Wm / Wr).
  • the “content of linear alkylene group having 4 or more carbon atoms” in the hydroxyl group-containing polyester resin (a1) molecule is, for example, the carbon in the acid component (a1-1) and alcohol component (a1-2). It can be adjusted by adjusting the blending ratio of the aliphatic dicarboxylic acid having a linear alkylene group having 4 or more and the aliphatic diol having a linear alkylene group having 4 or more carbon atoms.
  • the production of the hydroxyl group-containing polyester resin (a1) is not particularly limited, and can be performed according to a usual method.
  • a usual method there is a method of performing an esterification reaction or a transesterification reaction by reacting the acid component (a1-1) and the alcohol component (a1-2) in a nitrogen stream at 150 to 250 ° C. for 5 to 10 hours. Can be mentioned.
  • the acid component (a1-1) and alcohol component (a1-2) may be added at once, or may be added in several portions.
  • the carboxyl group-containing polyester resin may be esterified using the alcohol component (a1-2).
  • the acid anhydride may be reacted to half-esterify the hydroxyl group-containing polyester resin.
  • a catalyst may be used to promote the reaction.
  • the catalyst include known catalysts such as dibutyltin oxide, antimony trioxide, zinc acetate, manganese acetate, cobalt acetate, calcium acetate, lead acetate, tetrabutyl titanate and tetraisopropyl titanate.
  • the hydroxyl group-containing polyester resin (a1) can be modified with a fatty acid, a monoepoxy compound, a polyisocyanate compound, or the like during the preparation of the resin, or after the esterification reaction or the transesterification reaction.
  • fatty acid examples include coconut oil fatty acid, cottonseed oil fatty acid, hemp seed oil fatty acid, rice bran oil fatty acid, fish oil fatty acid, tall oil fatty acid, soybean oil fatty acid, linseed oil fatty acid, tung oil fatty acid, rapeseed oil fatty acid, castor oil fatty acid, dehydrated castor
  • oil fatty acids and safflower oil fatty acids examples include oil fatty acids and safflower oil fatty acids.
  • a glycidyl ester of a synthetic highly branched saturated fatty acid (trade name “Cardura E10”, manufactured by HEXION Specialty Chemicals) can be suitably exemplified.
  • polyisocyanate compound examples include aliphatic diisocyanates such as lysine diisocyanate, hexamethylene diisocyanate and trimethylhexane diisocyanate; hydrogenated xylylene diisocyanate, isophorone diisocyanate, methylcyclohexane-2,4-diisocyanate, methylcyclohexane-2,6.
  • aliphatic diisocyanates such as lysine diisocyanate, hexamethylene diisocyanate and trimethylhexane diisocyanate
  • hydrogenated xylylene diisocyanate isophorone diisocyanate
  • methylcyclohexane-2,4-diisocyanate methylcyclohexane-2,6.
  • Alicyclic diisocyanates such as diisocyanate, 4,4'-methylenebis (cyclohexyl isocyanate) and 1,3- (isocyanatomethyl) cyclohexane; aromatic diisocyanates such as tolylene diisocyanate, xylylene diisocyanate, diphenylmethane diisocyanate; lysine Organic polyisocyanate such as triisocyanate and higher polyisocyanate such as triisocyanate Itself or an adduct of each of these organic polyisocyanates with a polyhydric alcohol, a low molecular weight polyester resin or water, or a cyclized polymer (for example, isocyanurate) of each of the above organic diisocyanates, a biuret type adduct, etc. Is mentioned. These can be used alone or in combination of two or more.
  • the hydroxyl value of the hydroxyl group-containing polyester resin (a1) is in the range of 30 to 160 mgKOH / g.
  • the hydroxyl value is preferably in the range of 30 to 100 mgKOH / g, and in the range of 40 to 80 mgKOH / g. Is more preferable.
  • the number average molecular weight of the hydroxyl group-containing polyester resin (a1) is in the range of 1,000 to 6,000.
  • the number average molecular weight is preferably in the range of 2,000 to 6,000, preferably 2,500 to 5,000. More preferably within the range.
  • Adjustment of the hydroxyl value, number average molecular weight and acid value of the hydroxyl group-containing polyester resin (a1) can be achieved, for example, by comparing the equivalent ratio of the carboxyl group in the acid component (a1-1) and the hydroxyl group in the alcohol component (a1-2). It can be carried out by adjusting (COOH / OH); adjusting the reaction time in the esterification reaction or transesterification reaction.
  • the equivalent ratio (COOH / OH) of the carboxyl group in the acid component (a1-1) to the hydroxyl group in the alcohol component (a1-2) is generally preferably in the range of 0.80 to 1.0, It is more preferably in the range of 0.85 to 1.0, and still more preferably in the range of 0.90 to 1.0.
  • the number average molecular weight and the weight average molecular weight are values obtained by converting the number average molecular weight and the weight average molecular weight measured using a gel permeation chromatograph (GPC) based on the molecular weight of standard polystyrene. is there.
  • GPC gel permeation chromatograph
  • HLC8120GPC (trade name, manufactured by Tosoh Corporation) is used as a gel permeation chromatograph
  • TSKgel G-4000HXL “TSKgel G-3000HXL”
  • TSKgel G-2500HXL are used as columns.
  • TSKgel G-2000HXL (trade name, all manufactured by Tosoh Corporation)
  • mobile phase tetrahydrofuran
  • measurement temperature 40 ° C.
  • flow rate 1 mL / min
  • detector detector: RI can do.
  • melamine resin (a2) As a melamine resin (a2), the part obtained by reaction of a melamine and an aldehyde, or a complete methylol-ized melamine resin is mentioned, for example.
  • aldehyde examples include formaldehyde, paraformaldehyde, acetaldehyde, and benzaldehyde. Among these, formaldehyde is preferable.
  • melamine and formaldehyde In the reaction of melamine and formaldehyde, normally, a mononuclear melamine in which one melamine is methylolated and a polynuclear melamine in which two or more melamines are bonded by formaldehyde are generated.
  • an alkyl etherified melamine resin in which the methylol group of the partially or completely methylolated melamine resin is partially or completely etherified with an appropriate alcohol can be used.
  • Examples of the alcohol used for etherification include methyl alcohol, ethyl alcohol, n-propyl alcohol, iso-propyl alcohol, n-butyl alcohol, iso-butyl alcohol, 2-ethyl-1-butanol and 2-ethyl-1 -Hexanol and the like.
  • the content of mononuclear melamine in the melamine resin (a2) is preferably less than 40% by mass, and less than 35% by mass. It is preferable that it is less than 30% by mass.
  • the content ratio of mononuclear melamine in the melamine resin (a2) can be adjusted, for example, by changing the reaction conditions of the melamine and formaldehyde.
  • the content ratio of mononuclear melamine is, for example, by measuring the content of mononuclear melamine and polynuclear melamine using a gel permeation chromatograph for the reaction product of melamine and formaldehyde. Can be confirmed.
  • the melamine resin (a2) is preferably a melamine resin having at least one of an imino group and a methylol group from the viewpoint of smoothness and chipping resistance of the resulting multilayer coating film.
  • the melamine resin having at least one of the imino group and the methylol group can be obtained, for example, by partially etherifying the methylol group of the partially or completely methylolated melamine resin with the alcohol.
  • methyl alcohol, n-butyl alcohol and iso-butyl alcohol are preferable, and n-butyl alcohol and iso-butyl alcohol are more preferable from the viewpoint of water resistance of the resulting multilayer coating film. .
  • the melamine resin (a2) preferably has a weight average molecular weight of 400 to 6,000, more preferably 500 to 4,000, and further preferably 600 to 2,000.
  • a commercially available product can be used as the melamine resin (a2).
  • Examples of commercially available product names include “Cymel 202”, “Cymel 203”, “Cymel 204”, “Cymel 211”, “Cymel 238”, “Cymel 251”, “Cymel 303”, “Cymel 323”, “Cymel 324”, “Cymel 325”, “Cymel 327”, “Cymel 350”, “Cymel 385”, “Cymel 1156”, “Cymel 1158”, “Cymel 1116”, “Cymel 1130” , "Uban 120", “Uban 20HS”, “Uban 20SE60”, “Uban 2021”, “Uban 2028”, and “Uban 28-60” (all manufactured by Mitsui Chemicals, Inc.).
  • the organic solvent-type first colored paint (A) used in the method for forming a multilayer coating film of the present invention is an organic solvent-type paint containing the hydroxyl group-containing polyester resin (a1) and the melamine resin (a2).
  • the organic solvent-type paint is a term contrasted with a water-based paint, and is a paint that does not substantially contain water as a solvent.
  • the mixing ratio of the hydroxyl group-containing polyester resin (a1) and the melamine resin (a2) in the organic solvent-type first colored paint (A) is 100 parts by mass of the total solid content of the hydroxyl group-containing polyester resin (a1) and the melamine resin (a2).
  • Hydroxyl-containing polyester resin (a1) 30 to 90 parts by mass is preferable, 35 to 85 parts by mass is more preferable, and 45 to 75 parts by mass is even more preferable.
  • the organic solvent-type first colored paint (A) can contain a modifying resin in addition to the hydroxyl group-containing polyester resin (a1).
  • a modifying resin include acrylic resin, polyurethane resin, alkyd resin, silicon resin, fluorine resin, and epoxy resin.
  • acrylic resin and a polyurethane resin is included from the viewpoints of smoothness and chipping resistance of the resulting coating film.
  • the compounding amount of the modifying resin is the hydroxyl group-containing polyester resin (a1) in the organic solvent-type first colored paint (A).
  • it is preferably in the range of 1 to 50 parts by weight, more preferably in the range of 3 to 35 parts by weight, based on 100 parts by weight of the total solid content of the melamine resin (a2). More preferably, it is within the range of parts by mass.
  • the organic solvent-type first colored paint (A) can contain a curing agent other than the melamine resin (a2).
  • the curing agent include polyisocyanate compounds, blocked polyisocyanate compounds, and carbodiimide group-containing compounds.
  • the organic solvent-type first colored paint (A) preferably contains a curing catalyst from the viewpoint of chipping resistance, smoothness and water resistance of the formed multilayer coating film.
  • the curing catalyst include sulfonic acids such as p-toluenesulfonic acid, dodecylbenzenesulfonic acid, and dinonylnaphthalenesulfonic acid; alkylphosphoric acids such as monobutylphosphoric acid, dibutylphosphoric acid, mono-2-ethylhexylphosphoric acid, and di2-ethylhexylphosphoric acid. Acid esters; salts of these acids with amine compounds, and the like.
  • the compounding quantity of a curing catalyst is the hydroxyl-containing polyester resin (a1) and melamine resin in organic solvent type 1st colored paint (A).
  • a curing catalyst is the hydroxyl-containing polyester resin (a1) and melamine resin in organic solvent type 1st colored paint (A).
  • it is preferably in the range of 0.1 to 5 parts by weight, more preferably in the range of 0.3 to 3 parts by weight, based on 100 parts by weight of the total solid content of (a2). More preferably, it is in the range of 5 to 2 parts by mass.
  • the organic solvent-type first colored paint (A) preferably further contains a pigment.
  • the pigment include coloring pigments, extender pigments, and bright pigments. These can be used alone or in combination of two or more.
  • the compounding amount of the pigment is the hydroxyl group-containing polyester resin (a1) and melamine resin (a2) in the organic solvent-type first colored paint (A).
  • the compounding amount of the pigment is the hydroxyl group-containing polyester resin (a1) and melamine resin (a2) in the organic solvent-type first colored paint (A).
  • the compounding amount of the pigment is the hydroxyl group-containing polyester resin (a1) and melamine resin (a2) in the organic solvent-type first colored paint (A).
  • the compounding amount of the pigment is the hydroxyl group-containing polyester resin (a1) and melamine resin (a2) in the organic solvent-type first colored paint (A).
  • the color pigment examples include titanium oxide, zinc white, carbon black, molybdenum red, Prussian blue, cobalt blue, azo pigment, phthalocyanine pigment, quinacridone pigment, isoindoline pigment, selenium pigment, and perylene pigment. And dioxazine pigments and diketopyrrolopyrrole pigments. Of these, titanium oxide and carbon black are preferable.
  • the compounding amount of the colored pigment is the hydroxyl group-containing polyester resin (a1) and melamine resin (a2) in the organic solvent-type first colored paint (A).
  • the compounding amount of the colored pigment is the hydroxyl group-containing polyester resin (a1) and melamine resin (a2) in the organic solvent-type first colored paint (A).
  • the compounding amount of the colored pigment is the hydroxyl group-containing polyester resin (a1) and melamine resin (a2) in the organic solvent-type first colored paint (A).
  • the compounding amount of the colored pigment is the hydroxyl group-containing polyester resin (a1) and melamine resin (a2) in the organic solvent-type first colored paint (A).
  • examples of the extender pigment include talc, clay, kaolin, barium sulfate, barium carbonate, calcium carbonate, silica, and alumina white.
  • the compounding amount of the extender pigment is the hydroxyl group-containing polyester resin (a1) and melamine resin (a2) in the organic solvent-type first colored paint (A).
  • the compounding amount of the extender pigment is the hydroxyl group-containing polyester resin (a1) and melamine resin (a2) in the organic solvent-type first colored paint (A).
  • the compounding amount of the extender pigment is the hydroxyl group-containing polyester resin (a1) and melamine resin (a2) in the organic solvent-type first colored paint (A).
  • the compounding amount of the extender pigment is the hydroxyl group-containing polyester resin (a1) and melamine resin (a2) in the organic solvent-type first colored paint (A).
  • the range of 1 to 150 parts by weight preferably in the range of 5 to 130 parts by weight, and in the range of 10 to 110 parts by weight. More preferably.
  • the bright pigment examples include aluminum (including vapor-deposited aluminum), copper, zinc, brass, nickel, aluminum oxide, mica, aluminum oxide coated with titanium oxide and iron oxide, titanium oxide and iron oxide. Mention may be made of coated mica, glass flakes and hologram pigments. These glitter pigments can be used alone or in combination of two or more.
  • the aluminum pigment includes non-leafing aluminum and leafing aluminum, and any of them can be used.
  • the blending amount of the glitter pigment is the hydroxyl group-containing polyester resin (a1) and melamine resin in the organic solvent-type first colored paint (A).
  • it is preferably in the range of 1 to 50 parts by weight, more preferably in the range of 2 to 30 parts by weight, based on 100 parts by weight of the total solid content of (a2). More preferably, it is within the range.
  • the organic solvent-type first colored paint (A) preferably contains a flat pigment from the viewpoint of chipping resistance of the resulting multilayer coating film.
  • a flat pigment among the pigments, for example, talc, aluminum oxide, mica, aluminum oxide coated with titanium oxide or iron oxide, and mica coated with titanium oxide or iron oxide can be used. Of these, talc is preferably used.
  • the compounding amount of the flat pigment is the hydroxyl group-containing polyester resin (a1) and melamine resin (in the organic solvent-type first colored paint (A)).
  • it is preferably in the range of 0.5 to 20 parts by weight, more preferably in the range of 1 to 15 parts by weight, based on 100 parts by weight of the total solid content of a2). More preferably, it is in the range.
  • the organic solvent-type first colored paint (A) described above can be applied onto the object by a method known per se, for example, air spray, airless spray, rotary atomizer and the like. Electrostatic application may be performed during coating. Among these, electrostatic coating by air spray and electrostatic coating by a rotary atomizing coating machine are preferable, and electrostatic coating by a rotary atomizing coating machine is particularly preferable.
  • the coating film thickness is usually a cured film thickness, preferably in the range of 10 to 100 ⁇ m, more preferably in the range of 10 to 50 ⁇ m, and even more preferably in the range of 15 to 35 ⁇ m.
  • the coated organic solvent type first colored paint (A) is coated by means of, for example, preheating (preheating) or air blowing before applying the organic solvent type second colored paint (B).
  • preheating preheating
  • air blowing air blowing
  • the method for forming a multilayer coating film according to the present invention has the advantage that a multilayer coating film having excellent smoothness can be formed without performing the preheating.
  • the term “cured coating film” refers to the cured and dried state specified in JIS K 5600-1-1, that is, the center of the coating surface is strongly sandwiched between the thumb and index finger, and the coating surface has dents due to fingerprints. It is a coating film in which the movement of the coating film is not felt, and the center of the coating surface is rubbed rapidly with a fingertip so that no trace is left on the coating surface.
  • the uncured coating film is a state in which the coating film has not reached the above-mentioned cured and dried state, and includes a dry-to-touch state and a semi-cured and dried state defined in JIS K 5600-1-1.
  • step (2) of the method for forming a multilayer coating film of the present invention (b1) the hydroxyl value is within the range of 40 to 200 mgKOH / g on the uncured first colored coating film formed in the step (1).
  • An organic solvent-type second colored paint (B) containing is applied to form an uncured second colored coating film.
  • the hydroxyl group-containing acrylic resin (b1) is a hydroxyl group-containing acrylic resin having a hydroxyl value in the range of 40 to 200 mgKOH / g and a weight average molecular weight in the range of 3,000 to 15,000.
  • the hydroxyl group-containing acrylic resin (b1) usually contains a hydroxyl group-containing polymerizable unsaturated monomer and another polymerizable unsaturated monomer copolymerizable with the hydroxyl group-containing polymerizable unsaturated monomer, for example, in a solution weight in an organic solvent. It can be produced by copolymerization by a known method such as a legal method.
  • the hydroxyl group-containing polymerizable unsaturated monomer is a compound having at least one hydroxyl group and one polymerizable unsaturated bond in one molecule.
  • Examples of the hydroxyl group-containing polymerizable unsaturated monomer include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 3-hydroxypropyl (meth) acrylate and 4-hydroxybutyl (meth) acrylate.
  • Monoesterified products of (meth) acrylic acid and dihydric alcohols having 2 to 8 carbon atoms such as ⁇ -caprolactone modified products of these monoesterified products; N-hydroxymethyl (meth) acrylamide; allyl alcohol; Examples thereof include (meth) acrylate having a polyoxyethylene chain which is a hydroxyl group.
  • polymerizable unsaturated monomers copolymerizable with the hydroxyl group-containing polymerizable unsaturated monomer include, for example, methyl (meth) acrylate, ethyl (meth) acrylate, n-propyl (meth) acrylate, i-propyl.
  • Carboxyl group-containing polymerizable unsaturated monomers (meth) acrylonitrile, (meth) acrylamide, N, N-dimethylaminoethyl (meth) acrylate, N, N-dimethylaminopropyl (meth) acrylamide and Nitrogen-containing polymerizable unsaturated monomers such as amine adducts of silyl (meth) acrylate; 1 polymerizable unsaturated group such as allyl (meth) acrylate and 1,6-hexanediol di (meth) acrylate Polymerizable unsaturated monomer having two or more in the molecule; glycidyl (meth) acrylate, ⁇ -methylglycidyl (meth) acrylate, 3,4-epoxycyclohexylmethyl (meth) acrylate, 3,4-epoxycyclohexylethyl (meth) Epoxy group-containing polymerizable unsaturated mono
  • the hydroxyl value of the hydroxyl group-containing acrylic resin (b1) is in the range of 40 to 200 mgKOH / g.
  • the hydroxyl value is preferably in the range of 60 to 180 mgKOH / g, and in the range of 70 to 150 mgKOH / g. Is more preferable.
  • the hydroxyl value of the hydroxyl group-containing acrylic resin (b1) is preferably higher than the hydroxyl value of the hydroxyl group-containing polyester resin (a1).
  • the ratio of the hydroxyl value of the hydroxyl group-containing polyester resin (a1) to the hydroxyl value of the hydroxyl group-containing acrylic resin (b1) is within the range of 1 / 1.1-1 / 5 as the ratio of the former / the latter. Preferably, it is in the range of 1 / 1.2 to 1/4, and more preferably in the range of 1 / 1.5-1 to 1/3.
  • the weight average molecular weight of the hydroxyl group-containing acrylic resin (b1) is in the range of 3,000 to 15,000. Among these, from the viewpoint of smoothness and chipping resistance of the multilayer coating film to be formed, the number average molecular weight is preferably in the range of 3,500 to 12,000, and is preferably 4,000 to 8,000. More preferably within the range.
  • the melamine resin (b2) is a melamine resin having a mononuclear melamine content of 40% by mass or more.
  • a melamine resin having a mononuclear melamine content of 40% by mass or more in the melamine resin (a2) can be used.
  • the content ratio of the mononuclear melamine can be adjusted, for example, by changing the reaction conditions of the melamine and formaldehyde.
  • the content ratio of mononuclear melamine is, for example, by measuring the content of mononuclear melamine and polynuclear melamine using a gel permeation chromatograph for the reaction product of melamine and formaldehyde. Can be confirmed.
  • the content of the mononuclear melamine in the melamine resin (b2) is preferably in the range of 45 to 90% by mass, and is preferably 50 to 80% by mass. More preferably within the range.
  • the content ratio of mononuclear melamine in the melamine resin (b2) is obtained by, for example, reacting the melamine with formaldehyde and then reacting the reaction product containing mononuclear melamine and polynuclear melamine with gel permeation chromatography. It can be adjusted by taking a graph and varying the blending ratio of the mononuclear melamine and polynuclear melamine.
  • the melamine resin (b2) preferably has a weight average molecular weight of 400 to 2,000, more preferably 500 to 1,500, from the viewpoint of smoothness of the resulting multilayer coating film. More preferably, it is 600 to 1,000.
  • the acid catalyst (b3) include sulfonic acids such as p-toluenesulfonic acid, dodecylbenzenesulfonic acid and dinonylnaphthalenesulfonic acid; monobutylphosphoric acid, dibutylphosphoric acid, mono-2-ethylhexylphosphoric acid, and di-2-ethylhexylphosphoric acid. Alkyl phosphate esters of these; salts of these acids with amine compounds and the like can be used. Of these, sulfonic acid catalysts are preferred from the viewpoint of the smoothness of the resulting multilayer coating film.
  • sulfonic acid-based catalyst examples include sulfonic acids such as paratoluenesulfonic acid, dodecylbenzenesulfonic acid and dinonylnaphthalenesulfonic acid, and salts of the sulfonic acid and an amine compound.
  • Organic solvent type second colored paint (B) used in the multilayer coating film forming method of the present invention is an organic solvent type containing the hydroxyl group-containing acrylic resin (b1), melamine resin (b2) and acid catalyst (b3). It is a paint.
  • the mixing ratio of the hydroxyl group-containing acrylic resin (b1), the melamine resin (b2) and the acid catalyst (b3) in the organic solvent-type second colored paint (B) is the sum of the hydroxyl group-containing acrylic resin (b1) and the melamine resin (b2). It is preferable that it is in the following range on the basis of 100 mass parts of solid content. By making it in the said range, the coating film excellent in smoothness can be formed.
  • Hydroxyl group-containing acrylic resin (b1) 30 to 95 parts by mass is preferable, 35 to 85 parts by mass is more preferable, and 45 to 75 parts by mass is even more preferable.
  • Melamine resin (b2) 5 to 70 parts by mass is preferable, 15 to 65 parts by mass is more preferable, and 25 to 55 parts by mass is even more preferable.
  • the organic solvent-type second colored paint (B) can contain a modifying resin in addition to the hydroxyl group-containing acrylic resin (b1).
  • a modifying resin include polyester resin, polyurethane resin, alkyd resin, silicon resin, fluorine resin, and epoxy resin.
  • the compounding amount of the modifying resin is the hydroxyl group-containing acrylic resin (b1) in the organic solvent type second colored paint (B).
  • melamine resin (b2) based on 100 parts by mass of the total solid content it is generally preferably in the range of 1 to 50 parts by mass, more preferably in the range of 3 to 35 parts by mass. More preferably, it is within the range of 20 parts by mass.
  • the organic solvent type second colored paint (B) can contain a curing agent other than the melamine resin (b2).
  • a curing agent for example, a polyisocyanate compound, a blocked polyisocyanate compound, a carbodiimide group-containing compound, and the like can be used.
  • the organic solvent-type second colored paint (B) preferably further contains a pigment.
  • the pigment include coloring pigments, extender pigments and glitter pigments. These can be used alone or in combination of two or more.
  • the compounding amount of the pigment is the hydroxyl group-containing acrylic resin (b1) and melamine resin (b2) in the organic solvent-type second colored paint (B).
  • the compounding amount of the pigment is the hydroxyl group-containing acrylic resin (b1) and melamine resin (b2) in the organic solvent-type second colored paint (B).
  • the compounding amount of the pigment is the hydroxyl group-containing acrylic resin (b1) and melamine resin (b2) in the organic solvent-type second colored paint (B).
  • the compounding amount of the pigment is the hydroxyl group-containing acrylic resin (b1) and melamine resin (b2) in the organic solvent-type second colored paint (B).
  • color pigment examples include titanium oxide, zinc white, carbon black, molybdenum red, Prussian blue, cobalt blue, azo pigment, phthalocyanine pigment, quinacridone pigment, isoindoline pigment, selenium pigment, and perylene pigment. And dioxazine pigments and diketopyrrolopyrrole pigments.
  • the compounding amount of the color pigment is the hydroxyl group-containing acrylic resin (b1) and melamine resin (b2) in the organic solvent-type second colored paint (B).
  • the compounding amount of the color pigment is the hydroxyl group-containing acrylic resin (b1) and melamine resin (b2) in the organic solvent-type second colored paint (B).
  • the compounding amount of the color pigment is the hydroxyl group-containing acrylic resin (b1) and melamine resin (b2) in the organic solvent-type second colored paint (B).
  • the compounding amount of the color pigment is the hydroxyl group-containing acrylic resin (b1) and melamine resin (b2) in the organic solvent-type second colored paint (B).
  • examples of the extender pigment include clay, kaolin, barium sulfate, barium carbonate, calcium carbonate, talc, silica, and alumina white.
  • the compounding amount of the extender pigment is the hydroxyl group-containing acrylic resin (b1) and melamine resin (b2) in the organic solvent type second colored paint (B).
  • the compounding amount of the extender pigment is the hydroxyl group-containing acrylic resin (b1) and melamine resin (b2) in the organic solvent type second colored paint (B).
  • the compounding amount of the extender pigment is the hydroxyl group-containing acrylic resin (b1) and melamine resin (b2) in the organic solvent type second colored paint (B).
  • the bright pigment examples include aluminum (including vapor-deposited aluminum), copper, zinc, brass, nickel, aluminum oxide, mica, titanium oxide, and iron oxide coated with titanium oxide and iron oxide. Mention may be made of coated mica, glass flakes, hologram pigments and the like. These glitter pigments can be used alone or in combination of two or more.
  • Aluminum pigments include non-leafing aluminum and leafing aluminum, both of which can be used. Among these, aluminum, aluminum oxide, mica, aluminum oxide coated with titanium oxide and iron oxide, and mica coated with titanium oxide and iron oxide are preferable, and aluminum is particularly preferable.
  • the blending amount of the glitter pigment is the hydroxyl group-containing acrylic resin (b1) and melamine resin in the organic solvent-type second colored paint (B).
  • it is preferably in the range of 1 to 100 parts by weight, more preferably in the range of 2 to 50 parts by weight, based on 100 parts by weight of the total solid content of (b2). More preferably, it is within the range.
  • the organic solvent-type second colored paint (B) preferably further contains a flat pigment from the viewpoint of chipping resistance of the resulting multilayer coating film.
  • a flat pigment among the pigments, for example, talc, aluminum oxide, mica, aluminum oxide coated with titanium oxide or iron oxide, and mica coated with titanium oxide or iron oxide can be used. Of these, talc is preferably used.
  • the blending amount of the flat pigment is the hydroxyl group-containing acrylic resin (b1) and melamine resin (b) in the organic solvent-type second colored paint (B).
  • the blending amount of the flat pigment is the hydroxyl group-containing acrylic resin (b1) and melamine resin (b) in the organic solvent-type second colored paint (B).
  • it is preferably in the range of 0.5 to 20 parts by weight, more preferably in the range of 1 to 15 parts by weight, based on 100 parts by weight of the total solid content of b2). More preferably, it is in the range.
  • the solid content of the organic solvent-type second colored paint (B) is preferably in the range of 20 to 80% by mass, and in the range of 30 to 70% by mass, from the viewpoint of the smoothness of the resulting coating film. More preferably, it is more preferably in the range of 40 to 60% by mass.
  • the organic solvent type second colored paint (B) described above is a method known per se, for example, air spray, airless spray, and rotary atomization coating, on the coating film of the organic solvent type first colored paint (A). It can be applied by a machine or the like, and electrostatic application may be performed during the application. Among these, electrostatic coating by air spray and electrostatic coating by a rotary atomizing coating machine are preferable, and electrostatic coating by a rotary atomizing coating machine is particularly preferable.
  • the coating film thickness is usually a cured film thickness, preferably within the range of 5 to 80 ⁇ m, more preferably within the range of 6 to 50 ⁇ m, and even more preferably within the range of 10 to 35 ⁇ m.
  • the coated organic solvent type second colored paint (B) is coated with a solid content of the paint film by means of, for example, preheating (preheating) or air blowing before the clear coat paint (C) is applied.
  • preheating preheating
  • air blowing air blowing
  • the rate can be adjusted, from the viewpoint of energy saving, it is preferable not to perform the preheating, air blowing, or the like after the application of the organic solvent type second colored paint (B).
  • the method for forming a multilayer coating film according to the present invention has the advantage that a multilayer coating film having excellent smoothness can be formed without performing the preheating.
  • the multilayer coating film forming method of the present invention can form a multilayer coating film excellent in smoothness and chipping resistance without preheating in a three-coat one-bake method.
  • the organic solvent-type first colored paint (A) contains a relatively low molecular weight hydroxyl group-containing polyester resin (a1) containing a linear alkylene group having 4 or more carbon atoms, so that smoothness is improved. Can do.
  • the organic solvent-type second colored paint (B) contains a hydroxyl group-containing acrylic resin (b1) which is a different type of resin from the polyester resin, the first colored coating film is used without preheating. Even when the organic solvent-type second colored paint (B) is applied on top, it is presumed that a multilayer coating between the coating films hardly occurs and a multilayer coating film having excellent smoothness is formed.
  • the organic solvent-type second colored paint (B) contains a relatively low molecular weight melamine resin (b2) having a mononuclear melamine content of 40% by mass or more, smoothness can be improved. it can.
  • the acid catalyst (b3) in the organic solvent type second colored paint (B) is replaced with the hydroxyl group-containing polyester resin (a1) in the organic solvent type first colored paint (A) and the organic solvent type second colored paint (B).
  • Step (3) In the step (3) of the multilayer coating film forming method of the present invention, the clear coat paint (C) is applied onto the uncured second colored coating film formed in the above step (2).
  • thermosetting clear coat paint composition for painting automobile bodies and the like can be used.
  • thermosetting clear coat coating composition include an organic solvent-type thermosetting coating composition containing a base resin having a crosslinkable functional group and a crosslinking agent, an aqueous thermosetting coating composition, and a powder thermosetting. Can be mentioned.
  • Examples of the crosslinkable functional group possessed by the base resin include a carboxyl group, a hydroxyl group, an epoxy group, and a silanol group.
  • Examples of the base resin include acrylic resin, polyester resin, alkyd resin, urethane resin, epoxy resin, and fluororesin.
  • crosslinking agent examples include polyisocyanate compounds, blocked polyisocyanate compounds, melamine resins, urea resins, carboxyl group-containing compounds, carboxyl group-containing resins, epoxy group-containing resins, and epoxy group-containing compounds.
  • a hydroxyl group-containing resin / polyisocyanate compound As the base resin / crosslinking agent combination of the clear coat paint (C), a hydroxyl group-containing resin / polyisocyanate compound, a hydroxyl group-containing resin / blocked polyisocyanate compound, a hydroxyl group-containing resin / melamine resin, and the like are preferable.
  • the clear coat paint (C) may be a one-component paint or a multi-component paint such as a two-component urethane resin paint.
  • the clear coat paint (C) can contain a color pigment, a bright pigment, a dye, and the like, as needed, to the extent that transparency is not hindered.
  • an extender pigment, an ultraviolet absorber, A light stabilizer, an antifoaming agent, a thickening agent, a rust preventive agent, a surface conditioner, and the like can be appropriately contained.
  • the clear coat paint (C) can be applied onto the coating film of the organic solvent type second colored paint (B) by a method known per se, for example, airless spray, air spray and rotary atomizing coater. Electrostatic application may be performed during coating.
  • the film thickness of the coating with the clear coat paint (C) is usually a cured film thickness of preferably 10 to 80 ⁇ m, more preferably 15 to 60 ⁇ m, and more preferably 20 to 50 ⁇ m. Is more preferable.
  • Step (4) In the step (4) of the multilayer coating film forming method of the present invention, the uncured first colored coating film, the uncured second colored coating film and the uncured film formed in the above steps (1) to (3). These clear coatings are heated and cured simultaneously.
  • the first colored coating film, the second colored coating film, and the clear coating film can be cured by a normal coating film baking means such as hot air heating, infrared heating, and high-frequency heating.
  • the heating temperature is preferably 80 to 180 ° C, more preferably 100 to 170 ° C, and further preferably 120 to 160 ° C.
  • the heating time is preferably 10 to 60 minutes, more preferably 15 to 40 minutes.
  • the article to be coated to which the method of the present invention is applied is not particularly limited.
  • the object to be coated include an outer plate part of an automobile body such as a passenger car, a truck, a motorcycle and a bus; an automobile part such as a bumper; an outer plate part of a home electric product such as a mobile phone and an audio device. .
  • the outer plate of the automobile body and the automobile parts are preferable.
  • the material of the object to be coated is not particularly limited.
  • metal materials such as iron, aluminum, brass, copper, tinplate, stainless steel, galvanized steel and zinc alloy (such as Zn—Al, Zn—Ni and Zn—Fe) plated steel; polyethylene resin, polypropylene resin, acrylonitrile— Resins such as butadiene-styrene (ABS) resin, polyamide resin, acrylic resin, vinylidene chloride resin, polycarbonate resin, polyurethane resin and epoxy resin, mixtures of these resins, and plastic materials such as various fiber reinforced plastics (FRP); Examples thereof include inorganic materials such as glass, cement and concrete; wood; fiber materials such as paper and cloth. Among these, a metal material and a plastic material are preferable.
  • the object to be coated may be one in which surface treatment such as phosphate treatment, chromate treatment, and complex oxide treatment is performed on the metal surface of the metal material or a vehicle body formed from the metal material, and further, A coating film may be formed thereon.
  • surface treatment such as phosphate treatment, chromate treatment, and complex oxide treatment
  • Examples of the coated material on which the coating film has been formed include those in which a surface treatment is applied to the substrate as necessary and an undercoat coating film is formed thereon.
  • an undercoat coating film an electrodeposition coating film is preferable and the electrodeposition coating material by a cationic electrodeposition coating material is more preferable.
  • the object to be coated may be obtained by subjecting the plastic surface of the plastic material or an automobile part or the like molded from the plastic material to surface treatment and primer coating as necessary. Further, a combination of the plastic material and the metal material may be used.
  • a first colored paint (A-1) having a viscosity according to 4 of 20 seconds was obtained.
  • melamine resin (b2-1) (the content ratio of mononuclear melamine is 65%, weight average molecular weight 900, melamine resin having a methylol group, solid content 100%) 30 parts, “GX-180A” (trade name, manufactured by Asahi Kasei Metals, aluminum pigment paste, aluminum content 74%) 19 parts ( 14 parts of solid content) and 4 parts of “Nacure 5543” (trade name, manufactured by King Industries, amine salt of dodecylbenzenesulfonic acid, active ingredient 25%) were mixed uniformly.
  • (Note 8) Melamine resin (b2-2): 45% nucleamine melamine content, weight average molecular weight 800, melamine resin having imino group and methylol group, solid content 80% (Note 9)
  • test plate First colored paints (A-1) to (A-19) obtained in Production Examples 21 to 39, and second colored paints (B-1) to (B-17) obtained in Production Examples 40 to 56 were used. Using each, test plates were prepared and evaluated as follows.
  • Cathode electrodeposition paint (trade name “Electron GT-10” manufactured by Kansai Paint Co., Ltd.) was electrodeposited onto the cold-rolled steel sheet that had been subjected to zinc phosphate conversion treatment to a cured film thickness of 20 ⁇ m, and the temperature was 170 ° C. It was cured by heating for 30 minutes to obtain a test article.
  • Example 1 The organic solvent-type first colored paint (A-1) obtained in Production Example 21 is applied to the above test object using a rotary atomizing type electrostatic coating machine so that the cured film thickness becomes 25 ⁇ m. Electrostatic coating was applied and left for 3 minutes. Next, the organic solvent type second colored paint (B-1) obtained in Production Example 40 was applied on the uncured first colored coating film using a rotary atomizing type electrostatic coating machine to a cured film thickness of 15 ⁇ m. Then, it was electrostatically coated and left for 5 minutes.
  • a hydroxyl group-containing acrylic resin / polyisocyanate compound-based organic solvent-type overcoat clear coat paint (trade name “KINO-5071”, manufactured by Kansai Paint Co., Ltd., hereinafter “clear coat paint” is applied to the uncured second colored coating film.
  • C-1) a hydroxyl group-containing acrylic resin / polyisocyanate compound-based organic solvent-type overcoat clear coat paint (trade name “KINO-5071”, manufactured by Kansai Paint Co., Ltd., hereinafter “clear coat paint” is applied to the uncured second colored coating film.
  • C-1 a hydroxyl group-containing acrylic resin / polyisocyanate compound-based organic solvent-type overcoat clear coat paint
  • C-1 a hydroxyl group-containing acrylic resin / polyisocyanate compound-based organic solvent-type overcoat clear coat paint
  • Example 1 (Examples 2 to 25, Comparative Examples 1 to 10)
  • the first colored paint (A-1) obtained in Production Example 21 was changed to any of the first colored paints (A-2) to (A-19) shown in Table 5 below. 40, except that the second colored paint (B-1) obtained in 40 was changed to one of the second colored paints (B-1) to (B-17) shown in Table 5 below.
  • a test plate was prepared.
  • A The size of the scratch is extremely small, and the electrodeposition surface and the base steel plate are not exposed.
  • ⁇ The size of the scratch is small, and the electrodeposition surface and the base steel plate are not exposed.
  • X The size of the scratch is quite large, and the base steel plate is also greatly exposed.
  • Flip-flop property Each test plate was visually observed at different angles, and the flip-flop property was evaluated according to the following criteria.
  • Double-circle The change of the metallic feeling by a visual angle is remarkable (it has the very outstanding flip-flop property).
  • ⁇ The change of metallic feeling due to visual angle is large (excellent flip-flop property).
  • delta The change of the metallic feeling by a visual angle is a little small (flip-flop property is a little inferior).
  • X The change of the metallic feeling by a visual angle is small (flip-flop property is inferior).
  • Metallic unevenness Each test plate was visually observed, and the degree of occurrence of metallic unevenness was evaluated according to the following criteria. A: Almost no metallic unevenness is observed, and the coating film has an excellent appearance. ⁇ : Metallic unevenness is slightly observed, but has excellent coating appearance. (Triangle
  • the first colored paint, the second colored paint, and the clear paint are sequentially applied onto the article to be coated, and the resulting three-layered multilayer paint film is obtained. It was found that a multi-layer coating film excellent in smoothness, chipping resistance and water resistance can be formed in the three-coat one-bake method in which both are thermally cured.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)
  • Paints Or Removers (AREA)
PCT/JP2010/066713 2009-09-29 2010-09-27 複層塗膜形成方法 WO2011040374A1 (ja)

Priority Applications (4)

Application Number Priority Date Filing Date Title
IN2722DEN2012 IN2012DN02722A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) 2009-09-29 2010-09-27
US13/498,880 US8568833B2 (en) 2009-09-29 2010-09-27 Process for formation of multi-layered coating film
JP2011534234A JPWO2011040374A1 (ja) 2009-09-29 2010-09-27 複層塗膜形成方法
CN2010800436576A CN102548669A (zh) 2009-09-29 2010-09-27 多层涂膜的形成方法

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2009225632 2009-09-29
JP2009-225632 2009-09-29

Publications (1)

Publication Number Publication Date
WO2011040374A1 true WO2011040374A1 (ja) 2011-04-07

Family

ID=43826189

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2010/066713 WO2011040374A1 (ja) 2009-09-29 2010-09-27 複層塗膜形成方法

Country Status (5)

Country Link
US (1) US8568833B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
JP (1) JPWO2011040374A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
CN (1) CN102548669A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
IN (1) IN2012DN02722A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
WO (1) WO2011040374A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011167614A (ja) * 2010-02-17 2011-09-01 Mazda Motor Corp 積層塗膜形成方法
JP2012000568A (ja) * 2010-06-16 2012-01-05 Kansai Paint Co Ltd 複層塗膜形成方法
JP2019524475A (ja) * 2016-05-31 2019-09-05 ピーピージー コーティングス （ティエンジン） カンパニー， リミテッド ３ｃ１ｂコーティング、それを塗布する方法およびそれを用いてコーティングされた基材
US11541420B2 (en) 2018-05-09 2023-01-03 Kansai Paint Co., Ltd. Method for forming multilayer coated film

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5948164B2 (ja) * 2012-06-28 2016-07-06 Ｂａｓｆジャパン株式会社 複層塗膜形成方法
EP2837667A3 (de) * 2014-09-29 2015-04-22 Basf Se Einkomponentige Aminoharzbeschichtungsmassen
WO2018084062A1 (ja) * 2016-11-04 2018-05-11 Dic株式会社 ポリエステルポリオール樹脂及び塗料

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH10216617A (ja) * 1997-02-03 1998-08-18 Nof Corp ３層系塗膜の形成方法
JP2002153807A (ja) * 2000-11-20 2002-05-28 Nippon Paint Co Ltd 塗膜形成方法及び積層塗膜
JP2007075791A (ja) * 2005-09-16 2007-03-29 Nippon Paint Co Ltd 積層塗膜形成方法および塗装物

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW242644B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * 1992-10-30 1995-03-11 Ppg Industries Inc
JP3831266B2 (ja) 2002-01-22 2006-10-11 日本ペイント株式会社 塗膜形成方法
DE60335979D1 (de) * 2002-02-13 2011-03-24 Ppg Ind Ohio Inc Rbundbeschichtung auf einem träger
US7150899B2 (en) * 2002-11-05 2006-12-19 Kansai Paint Co., Ltd. Method for forming coating film on plastic substrate
CA2636245C (en) * 2006-01-23 2011-03-15 Kansai Paint Co., Ltd. Aqueous intermediate coating composition and method for forming multilayer coating film
JP5226954B2 (ja) * 2007-02-02 2013-07-03 永大産業株式会社 メラミン樹脂の製造方法
JP4875581B2 (ja) * 2007-09-28 2012-02-15 関西ペイント株式会社 複層塗膜形成方法

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH10216617A (ja) * 1997-02-03 1998-08-18 Nof Corp ３層系塗膜の形成方法
JP2002153807A (ja) * 2000-11-20 2002-05-28 Nippon Paint Co Ltd 塗膜形成方法及び積層塗膜
JP2007075791A (ja) * 2005-09-16 2007-03-29 Nippon Paint Co Ltd 積層塗膜形成方法および塗装物

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011167614A (ja) * 2010-02-17 2011-09-01 Mazda Motor Corp 積層塗膜形成方法
JP2012000568A (ja) * 2010-06-16 2012-01-05 Kansai Paint Co Ltd 複層塗膜形成方法
JP2019524475A (ja) * 2016-05-31 2019-09-05 ピーピージー コーティングス （ティエンジン） カンパニー， リミテッド ３ｃ１ｂコーティング、それを塗布する方法およびそれを用いてコーティングされた基材
US11541420B2 (en) 2018-05-09 2023-01-03 Kansai Paint Co., Ltd. Method for forming multilayer coated film

Also Published As

Publication number Publication date
CN102548669A (zh) 2012-07-04
JPWO2011040374A1 (ja) 2013-02-28
IN2012DN02722A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) 2015-09-11
US8568833B2 (en) 2013-10-29
US20120183796A1 (en) 2012-07-19

Similar Documents

Publication Publication Date Title
JP5081608B2 (ja) 複層塗膜形成方法
JP5885828B2 (ja) 複層塗膜形成方法、及び塗装物品
JP5612671B2 (ja) 複層塗膜形成方法
JP5594931B2 (ja) 水性ベース塗料組成物
JP5547398B2 (ja) 塗料組成物
JPWO2018135209A1 (ja) 水性塗料組成物及び複層塗膜形成方法
JP2011530393A (ja) 複層塗膜形成方法
WO2011040374A1 (ja) 複層塗膜形成方法
JP2014004552A (ja) 複層塗膜形成方法及び塗装物品
JP5349409B2 (ja) 複層塗膜形成方法
JPWO2007145368A1 (ja) 塗料組成物
WO2020162126A1 (ja) 水性塗料組成物
JP5547450B2 (ja) 着色塗料組成物
JP5507798B2 (ja) 水性塗料組成物
JP5476260B2 (ja) 樹脂組成物、該樹脂組成物を含有する水性塗料組成物及び複層塗膜形成方法
JP6738848B2 (ja) 複層塗膜形成方法
CA3148742C (en) Hydrophobic melamine containing aqueous coating compositions
JP2010082529A (ja) 複層塗膜形成方法及び塗装物品
JP7355968B1 (ja) 水性塗料組成物、塗膜形成方法及び複層塗膜形成方法
JP7352766B1 (ja) 複層塗膜形成方法
TWI895272B (zh) 水性塗料組成物
JP5113439B2 (ja) 複層塗膜形成方法
JP5547377B2 (ja) 着色塗料組成物
WO2024018708A1 (ja) 水性塗料組成物、塗膜形成方法及び複層塗膜形成方法
CA3171321A1 (en) Aqueous coating composition and method for forming multilayer coating film

Legal Events

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

Ref document number: 201080043657.6

Country of ref document: CN

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 10820489

Country of ref document: EP

Kind code of ref document: A1

WWE Wipo information: entry into national phase

Ref document number: 2011534234

Country of ref document: JP

WWE Wipo information: entry into national phase

Ref document number: 13498880

Country of ref document: US

NENP Non-entry into the national phase

Ref country code: DE

WWE Wipo information: entry into national phase

Ref document number: 2722/DELNP/2012

Country of ref document: IN

122 Ep: pct application non-entry in european phase

Ref document number: 10820489

Country of ref document: EP

Kind code of ref document: A1