WO2013189192A1 - 耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆及其制备方法 - Google Patents

耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆及其制备方法 Download PDF

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Publication number
WO2013189192A1
WO2013189192A1 PCT/CN2013/072422 CN2013072422W WO2013189192A1 WO 2013189192 A1 WO2013189192 A1 WO 2013189192A1 CN 2013072422 W CN2013072422 W CN 2013072422W WO 2013189192 A1 WO2013189192 A1 WO 2013189192A1
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component
water
acrylate
baking type
solution
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PCT/CN2013/072422
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English (en)
French (fr)
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黄菊梅
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Huang Jumei
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Priority to US14/391,799 priority Critical patent/US9238748B2/en
Priority to EP13807652.6A priority patent/EP2886565B1/en
Publication of WO2013189192A1 publication Critical patent/WO2013189192A1/zh

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    • 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
    • C09D133/00Coating 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 only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
    • C09D133/04Homopolymers or copolymers of esters
    • C09D133/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C09D133/08Homopolymers or copolymers of acrylic acid esters
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00Copolymers 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 a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10Esters
    • C08F220/12Esters of monohydric alcohols or phenols
    • C08F220/14Methyl esters, e.g. methyl (meth)acrylate
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00Copolymers 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 a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10Esters
    • C08F220/12Esters of monohydric alcohols or phenols
    • C08F220/16Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
    • C08F220/18Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
    • C08F220/1802C2-(meth)acrylate, e.g. ethyl (meth)acrylate
    • 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
    • C08L33/08Homopolymers or copolymers of acrylic acid esters
    • 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
    • C08L61/26Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds
    • C08L61/28Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds with melamine
    • 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
    • C09D133/00Coating 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 only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
    • C09D133/04Homopolymers or copolymers of esters
    • C09D133/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C09D133/062Copolymers with monomers not covered by C09D133/06
    • C09D133/066Copolymers with monomers not covered by C09D133/06 containing -OH groups
    • 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
    • C09D133/00Coating 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 only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
    • C09D133/04Homopolymers or copolymers of esters
    • C09D133/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C09D133/10Homopolymers or copolymers of methacrylic acid esters

Definitions

  • This invention relates to an aqueous coating composition, and more particularly to an aqueous two-component baking type automotive varnish having improved acid corrosion resistance and a method of producing the same.
  • varnish has been widely used in various products (such as: automobiles, plastics, glass products, etc.) to improve the appearance of decorative products and protect primers.
  • the existing varnish is mainly composed of a resin film-forming material and a solvent, and the film-forming material is generally formed by crosslinking and curing a polyester resin or an acrylic resin with an amino resin, and the acrylic resin is widely used for its good weather resistance; Generally it is a volatile organic solvent.
  • Existing varnishes mainly have the following disadvantages:
  • the surface is prone to pinholes, fish eyes, smooth and flat;
  • the existing varnish has the problems of small application range, poor scratch resistance, environmental protection and high cost.
  • the clear varnish coating for the automobile body is the final coating of the automobile body, which affects the appearance and decoration of the entire automobile, requires good gloss, and the coating is exposed to the air, and is exposed to acid rain and other air. Contaminants are required to have good acid corrosion resistance.
  • the solvent coating type varnish is often used for car painting. Although its performance is excellent, a large amount of volatile organic substances generated at the same time pollute the environment, and the environmentally-friendly water-based clear varnish currently on the market has higher production cost and lower performance than solvent. The type of clear varnish limits the application.
  • the object of the present invention is to provide a water-based two-component baking type automobile varnish with low cost and environmentally-friendly acid corrosion resistance in view of the high cost and environmentally-friendly defects of the existing automotive body finish varnish. And its preparation method.
  • the invention provides an aqueous two-component baking type automobile clear varnish with improved acid corrosion resistance, which is represented by weight percentage, and the water two-component baking type automobile varnish is composed of two components A and B Composition, the mass ratio between component A and component B is 1 to 4:1, wherein:
  • composition of the A component is: 20 to 30% of the methacrylate monomer, 35 to 45% of the acrylate monomer, 5 to 15% of the non-acrylate monomer, 15 to 15% of the acrylic monomer, Hydroxyl acrylate monomer 10 ⁇ 20% and chain transfer agent 0.5-1.5%;
  • composition of the B component is: methacrylate monomer 5 ⁇ : 15%, acrylate monomer 35 ⁇ 45%, non-acrylate monomer 5 ⁇ : 15%, acrylic monomer 5 ⁇ : 15%,
  • the hydroxyl group-containing acrylate monomer is 25 to 35% and the chain transfer agent is 0.5 to: 5%.
  • the methacrylate monomer is methyl methacrylate, ethyl methacrylate, isopropyl methacrylate, and Any of isobutyl acrylate and t-butyl methacrylate;
  • the acrylate monomer is any one of butyl acrylate, methyl acrylate, ethyl acrylate, isopropyl acrylate, n-propyl acrylate, 2-ethylhexyl acrylate and isobutyl acrylate;
  • the non-acrylate monomer is styrene or vinyl acetate
  • the acrylic monomer is acrylic acid, methacrylic acid or itaconic acid
  • the hydroxyl group-containing acrylate monomer is - ⁇ -hydroxyethyl acrylate, ⁇ -hydroxypropyl acrylate, ⁇ -hydroxyethyl methacrylate or ⁇ -hydroxypropyl methacrylate;
  • the chain transfer agent is dodecyl mercaptan, carbon tetrachloride, n-butyl mercaptan, tert-butyl mercaptan, carbon tetrabromide, n-butyl sulfide, cumene, ⁇ -naphthylthiophenol and Any of carbon tetraoxide.
  • the composition of the bismuth component is: methyl methacrylate 20 to 30%, butyl acrylate 35 to 45%, styrene 5 to: 15% , acrylic acid 5 ⁇ : 15%, methacrylic acid- ⁇ -hydroxyethyl ester 10 ⁇ 20% and dodecyl mercaptan 0.5 ⁇ : 1.5%;
  • composition of the bismuth component is: methyl methacrylate 5 ⁇ : 15%, butyl acrylate 35 ⁇ 45%, styrene 5 ⁇ : 15%, acrylic acid 5 ⁇ : 15%, methacrylic acid- ⁇ -hydroxyethyl ester 25 ⁇ 35% and dodecyl mercaptan 0.5 to: 1.5%.
  • the composition of the bismuth component is: methyl methacrylate 25%, butyl acrylate 40%, styrene 10%, acrylic acid 9%, methyl group Acrylic acid- ⁇ -hydroxyethyl ester 15% and dodecyl mercaptan 1.0%;
  • composition of the bismuth component is: methyl methacrylate 10%, butyl acrylate 40%, styrene 10%, acrylic acid 9%, methacrylic acid- ⁇ -hydroxyethyl ester 30% and dodecyl mercaptan 1.0%.
  • a method for preparing an aqueous two-component baking type automobile varnish improved in the above-mentioned acid corrosion resistance comprising the following steps:
  • the obtained solution A is subjected to a conventional solution polymerization reaction to obtain an acrylic resin A; then, the temperature is lowered to 50 to 60 ° C, a neutralizing agent is added, and the degree of neutralization of the acrylic resin A is adjusted to 60 to 100% to obtain a water-based acrylic resin A. ;
  • composition of the B component in the water-based two-component baking type automobile varnish improved by the above-mentioned acid corrosion resistance various raw materials are weighed, and the weighed various raw materials are mixed, and the obtained mixture is used as a solute, and the solute is obtained.
  • a solution is obtained, and the obtained solution has a mass concentration of 50 to 70%; then, the initiator is added to the solution by adding 0.3 ⁇ : 1.1% of the total mass of the solute, and the mixture is uniformly mixed to obtain a solution B;
  • the aqueous acrylic resin A obtained in the step a and the aqueous acrylic resin B obtained in the step b are mixed at a mass ratio of 1 to 4:1, and uniformly mixed to obtain a mixed aqueous acrylic resin, and then a cross-linking agent hexamethoxy is added.
  • Methyl melamine formaldehyde resin, the mixed water-based acrylic resin and the crosslinking agent are added in a mass ratio of 2 to 3:1, and finally diluted with water to a desired viscosity, and diluted to a desired viscosity to obtain an improved acid corrosion resistance of the product of the present invention.
  • Water-based two-component baking car varnish Water-based two-component baking car varnish.
  • the preparation method of the aqueous two-component baking type automobile clear varnish improved according to the above-mentioned acid resistance is propylene glycol methyl ether, isopropyl alcohol, ethanol, propanol, butanol, isobutanol, sec-butanol , tert-butanol, 1-ethoxy-2-propanol, 1-isopropoxy-2-propanol, 1-propoxy-2-propanol and 1-butoxy-2-propanol One or both;
  • the initiator is azobisisobutyronitrile, azobisisoheptanenitrile, benzoyl peroxide, di-tert-butyl peroxide, t-butyl peroxybenzoate, 60% dimethyl phthalate solution and Any of diisobutyryl peroxide;
  • the neutralizing agent is any one of dimethylethanolamine, morpholine, monoethylamine, diethylamine, triethylamine, diethylethanolamine, monoethanolamine, diethanolamine, triethanolamine and diisopropanolamine. .
  • the solvent is a mixture of propylene glycol methyl ether and isopropyl alcohol, and a mixture of propylene glycol methyl ether and isopropyl alcohol The ratio is 1 ⁇ 4:1;
  • the initiator is azobisisobutyronitrile; the neutralizing agent is dimethylethanolamine.
  • the solution polymerization reaction is carried out at a reaction temperature of 80 to 120 ° C and a reaction time of 6 to 8 hours.
  • the various raw materials of the component A of the present invention are mixed to obtain an aqueous acrylic resin A having a number average molecular weight of about 10,000, and various raw materials of the component B are mixed and reacted to obtain an aqueous acrylic resin B having a number average molecular weight of about 20,000, and an aqueous acrylic acid.
  • Resin A and water-based acrylic resin B are mixed and a crosslinking agent is added.
  • the group reacting with the crosslinking agent in the molecular chain of the resin is a hydroxyl group. According to the principle of structure and properties of the crosslinked polymer material, the molecular weight of the resin is high, and the mechanical properties of the polymer are obtained.
  • the aqueous acrylic resin A and the aqueous acrylic resin B are mixed at a mass ratio of 1 to 4:1, and the molecular weight of the acrylic resin B is higher and the number of hydroxyl groups in the molecular chain is more than that of the acrylic resin.
  • the number of A is doubled, and its proportion in the mixed resin is small, so that the viscosity of the mixed resin is not too large, which affects the sufficient occurrence of the crosslinking reaction, and at the same time, the average molecular weight and the varnish of the mixed resin can be improved.
  • the various raw materials of the component A of the present invention are mixed to obtain an aqueous acrylic resin A having a number average molecular weight of about 10,000, and various raw materials of the component B are mixed and reacted to obtain an aqueous acrylic resin B having a number average molecular weight of about 20,000.
  • a cross-linking agent hexamethoxymethyl melamine formaldehyde resin By adding a cross-linking agent hexamethoxymethyl melamine formaldehyde resin, two water-soluble acrylic resins having a number average molecular weight of about 10,000 and a number average molecular weight of about 20,000 are cross-linked with a crosslinking agent, so that the finally formed crosslinked structure is very Dense, the obtained coating film has excellent comprehensive properties, especially good acid corrosion resistance; and the raw material price is lower, which makes the production cost lower.
  • the water-based two-component baking type automobile varnish improved by the method of the present invention has a pencil hardness of 2H, an impact strength of 50 kg'cm, an adhesion level of 1 and a flexibility of 1 mm. Gloss 113 (60°); and excellent acid corrosion resistance.
  • a sulfuric acid solution with a mass fraction of 30% is used as the acidic medium, and the coating film is immersed for at least 56 hours at 25 ° C without blistering.
  • the water-based two-component baking type automobile varnish with improved acid corrosion resistance is prepared by using the technical scheme of the present invention, and a large amount of volatile organic substances which are not generated are polluted by the environment, and is an environmentally-friendly water-based clear varnish.
  • the water-based two-component baking type automobile varnish improved in acid corrosion resistance of the present embodiment expressed by weight percentage, the water-based two-component baking type automobile varnish SA and ⁇ two components, group
  • the mass ratio between the tiller and the component ⁇ is 3:1, where:
  • composition of component A is: methyl methacrylate 25%, butyl acrylate 40%, styrene 10%, acrylic acid 9%, methacrylic acid - ⁇ -hydroxyethyl ester 15% and dodecyl mercaptan 1.0%;
  • composition of the bismuth component is: methyl methacrylate 10%, butyl acrylate 40%, styrene 10%, acrylic acid 9%, methacrylic acid- ⁇ -hydroxyethyl ester 30% and dodecyl mercaptan 1.0%.
  • the method for preparing an aqueous two-component baking type automobile varnish improved in acid corrosion resistance comprising the following steps:
  • the various raw materials are weighed, and the obtained raw materials are mixed, and the obtained mixture is used as a mixture.
  • Solute the solute is dissolved in a mixture solvent of propylene glycol methyl ether and isopropyl alcohol (volume ratio when propylene glycol methyl ether and isopropyl alcohol are mixed is 2:1), and the solution is sufficiently dissolved to obtain a mass percentage of the obtained solution.
  • the concentration is 60%; then, the initiator azobisisobutyronitrile, which is 1.7% of the total mass of the solute, is uniformly mixed in the solution, and uniformly mixed to obtain a solution A; the obtained solution A is subjected to conventional solution polymerization to obtain an acrylic resin A (In the solution polymerization reaction, the reaction temperature is controlled to be 80 to: 120 ° C, and the reaction time is 6 to 8 h); then, the temperature is lowered to 50 to 60 ° C, and the neutralizing agent dimethylethanolamine is added to adjust the degree of neutralization of the resin to 70%. Obtaining a water-based acrylic resin A;
  • the various raw materials are weighed, and the various raw materials weighed are mixed to obtain a mixture as a solute.
  • the initiator azobisisobutyronitrile which is 0.5% of the total mass of the solute, is added to the solution and uniformly mixed, and the mixture is uniformly mixed to obtain a solution B.
  • the obtained solution B is subjected to a conventional solution polymerization to obtain an acrylic resin B (control reaction during solution polymerization)
  • the temperature is 80 ⁇ : 120°C, the reaction time is 6 ⁇ 8h); then the temperature is lowered to 50 ⁇ 60°C, the neutralizing agent is added, the neutralization degree of the resin is adjusted to 70%, and the aqueous acrylic resin B is obtained; c.
  • the obtained aqueous acrylic resin A and the aqueous acrylic resin B obtained in the step b are mixed at a mass ratio of 3:1, and after mixing, a mixed aqueous acrylic resin is obtained, and then a cross-linking agent hexamethoxymethyl melamine formaldehyde resin is added and mixed.
  • the water-based acrylic resin and the crosslinking agent are added in a mass ratio of 3:1, and finally diluted with water to a desired viscosity, and diluted to a desired viscosity to obtain water having improved acid corrosion resistance of the product of the present embodiment.
  • Embodiment 2 Basically the same as Embodiment 1, except that:
  • the water-based two-component baking type automobile varnish improved in acid corrosion resistance of the present embodiment expressed by weight percentage, the water-based two-component baking type automobile varnish SA and ⁇ two components, group
  • the mass ratio between the tiller and the component ⁇ is 4:1, where:
  • composition of component A is: methyl methacrylate 23%, butyl acrylate 45%, styrene 6.5%, acrylic acid 15%, methacrylic acid - ⁇ -hydroxyethyl ester 10% and dodecyl mercaptan 0.5%;
  • composition of the bismuth component is: methyl methacrylate 15%, butyl acrylate 37%, styrene 15%, acrylic acid 6%, methacrylic acid - ⁇ -hydroxyethyl ester 26.5% and dodecyl mercaptan 0.5%.
  • the preparation method of the aqueous two-component baking type automobile varnish improved in acid corrosion resistance of the present embodiment is different from that of the embodiment 1 in that:
  • step a dissolving the solute in a solvent mixture of propylene glycol methyl ether and isopropyl alcohol (the volume ratio of the mixture of propylene glycol methyl ether and isopropyl alcohol is 3:1), and fully dissolving to obtain a solution, and the quality of the obtained solution
  • the percentage concentration is 70%; then, the initiator is added to the solution, and the initiator is 1.2% of the total mass of the solute, and the tert-butyl peroxybenzoate is uniformly mixed; the obtained solution is subjected to conventional solution polymerization to obtain an acrylic resin A (control during solution polymerization)
  • the reaction temperature is 80 to: 120 ° C, the reaction time is 6 to 8 h); then the temperature is lowered to 50 to 60 ° C, the neutralizing agent diisopropanolamine is added, and the degree of neutralization of the solution is adjusted to 60%; A.
  • step b the solute is dissolved in a solvent mixture of propylene glycol methyl ether and isopropyl alcohol (the volume ratio of propylene glycol methyl ether and isopropyl alcohol is 3:1), and the solution is fully dissolved to obtain the mass of the solution.
  • the percentage concentration is 70%; then the initiator is added to the solution, which is 0.8% of the total mass of the solute, and the tert-butyl peroxybenzoate is uniformly mixed; the obtained solution is subjected to conventional solution polymerization to obtain an acrylic resin B (control during solution polymerization)
  • the reaction temperature is 80 to: 120 ° C, the reaction time is 6 to 8 h); then the temperature is lowered to 50 to 60 ° C, the neutralizing agent diisopropanolamine is added, and the degree of neutralization of the solution is adjusted to 60%; B
  • step c the aqueous acrylic resin A obtained in the step a and the aqueous acrylic resin B obtained in the step b are mixed at a mass ratio of 4:1, and the mass ratio of the mixed aqueous acrylic resin to the crosslinking agent is 2 :1.
  • Embodiment 3 Basically the same as Embodiment 1, except that: The water-based two-component baking type automobile varnish improved in acid corrosion resistance of the present embodiment, expressed by weight percentage, the water-based two-component baking type automobile varnish SA and ⁇ two components, group The mass ratio between the tiller and the component ⁇ is 2:1, where:
  • composition of component A is: methyl methacrylate 30%, butyl acrylate 35%, styrene 8.5%, acrylic acid 5%, methacrylic acid - ⁇ -hydroxyethyl ester 20% and dodecyl mercaptan 1.5%;
  • composition of the bismuth component is: methyl methacrylate 5%, butyl acrylate 45%, styrene 5%, acrylic acid 15%, methacrylic acid- ⁇ -hydroxyethyl ester 28.5% and dodecyl mercaptan 1.5%.
  • the preparation method of the aqueous two-component baking type automobile varnish improved in acid corrosion resistance of the present embodiment is different from that of the embodiment 1 in that:
  • step a dissolving the solute in a solvent mixture of propylene glycol methyl ether and isopropyl alcohol (the volume ratio of the mixture of propylene glycol methyl ether and isopropyl alcohol is 4:1), fully dissolving to obtain a solution, and the quality of the obtained solution
  • the percentage concentration is 50%; then, the initiator azobisisoheptonitrile is added to the solution to be uniformly mixed with 1.5% of the total mass of the solute; the obtained solution is subjected to conventional solution polymerization to obtain acrylic resin A (control reaction during solution polymerization)
  • the temperature is 80 to: 120 ° C, the reaction time is 6 to 8 h); then the temperature is lowered to 50 to 60 ° C, the neutralizing agent diethylethanolamine is added, and the degree of neutralization of the solution is adjusted to 80% to obtain an aqueous acrylic resin A.
  • step b dissolving the solute in a solvent mixture of propylene glycol methyl ether and isopropyl alcohol (the volume ratio of the mixture of propylene glycol methyl ether and isopropyl alcohol is 4:1), and fully dissolving to obtain a solution, and the quality of the obtained solution
  • the percentage concentration is 50%; then, the initiator azobisisoheptonitrile is added to the solution to be uniformly mixed with 1.0% of the total mass of the solute; the obtained solution is subjected to conventional solution polymerization to obtain an acrylic resin B (control reaction during solution polymerization)
  • the temperature is 80 ⁇ : 120 ° C, the reaction time is 6 ⁇ 8h); then the temperature is lowered to 50 ⁇ 60 ° C, the neutralizer diethylethanolamine is added, the neutralization degree of the solution is adjusted to 80%, and the aqueous acrylic resin B is obtained;
  • the aqueous acrylic resin A obtained in the step a and the aqueous acrylic resin B obtained in the step b are mixed at a ratio of 2:1 by mass, and then the crosslinking agent is added to mix the aqueous acrylic resin and the crosslinking agent.
  • Qualitative Embodiment 4 Basically the same as Embodiment 1, except that:
  • the water-based two-component baking type automobile varnish improved in acid corrosion resistance of the present embodiment expressed by weight percentage, the water-based two-component baking type automobile varnish SA and ⁇ two components, group
  • the mass ratio between the tiller and the component ⁇ is 1:1, where:
  • composition of component A is: methyl methacrylate 27%, butyl acrylate 38%, styrene 8%, acrylic acid 10%, methacrylic acid - ⁇ -hydroxyethyl ester 16% and dodecyl mercaptan 1.0%;
  • composition of the bismuth component is: methyl methacrylate 9%, butyl acrylate 39%, styrene 9%, acrylic acid 10%, methacrylic acid - ⁇ -hydroxyethyl ester 32% and dodecyl mercaptan 1.0%.
  • the preparation method of the aqueous two-component baking type automobile varnish improved in acid corrosion resistance of this embodiment is the same as that in the first embodiment.
  • Embodiment 5 Basically the same as Embodiment 1, except that:
  • the water-based two-component baking type automobile varnish is composed of two components A and B, and the mass ratio between the component A and the component B is 3:1, wherein :
  • composition of component A is: ethyl methacrylate 25%, methyl acrylate 40%, vinyl acetate 10%, methacrylic acid 9%, hydroxyethyl acrylate 15% and n-butyl thiol 1.0%;
  • composition of component B is: ethyl methacrylate 10%, methyl acrylate 40%, vinyl acetate 10%, methacrylic acid 9%, hydroxyethyl acrylate 30% and n-butyl thiol 1.0%.
  • the preparation method of the aqueous two-component baking type automobile varnish improved in acid corrosion resistance of this embodiment is the same as that in the first embodiment.
  • Embodiment 6 Basically the same as Embodiment 1, except that:
  • the water-based two-component baking type automobile varnish improved in acid corrosion resistance of the present embodiment expressed by weight percentage, the water-based two-component baking type automobile varnish SA and ⁇ two components, group
  • the mass ratio between the tiller and the component ⁇ is 2:1, where:
  • composition of component A is: isopropyl methacrylate 23%, ethyl acrylate 45%, styrene 6.5%, itaconic acid 15%, hydroxypropyl acrylate 10% and n-butyl sulfide 0.5%;
  • composition of component B is: isopropyl methacrylate 15%, ethyl acrylate 37%, styrene 15%, itaconic acid 6%, hydroxypropyl acrylate 26.5% and n-butyl sulfide 0.5%.
  • the preparation method of the aqueous two-component baking type automobile varnish improved in acid corrosion resistance of this embodiment is the same as that in the first embodiment.
  • Embodiment 7 Basically the same as Embodiment 1, except that:
  • the water-based two-component baking type automobile varnish improved in acid corrosion resistance of the present embodiment expressed by weight percentage, the water-based two-component baking type automobile varnish SA and ⁇ two components, group
  • the mass ratio between the tiller and the component ⁇ is 4:1, where:
  • composition of component A is: isobutyl methacrylate 30%, isobutyl acrylate 35%, styrene 8.5%, acrylic acid 5%, methacrylic acid - ⁇ -hydroxypropyl ester 20% and cumene 1.5%;
  • composition of the bismuth component is: isobutyl methacrylate 5%, isobutyl acrylate 45%, styrene 5%, acrylic acid 15%, methacrylic acid - ⁇ -hydroxypropyl ester 28.5% and cumene 1.5%.
  • the preparation method of the aqueous two-component baking type automobile varnish improved in acid corrosion resistance of this embodiment is the same as that in the first embodiment.
  • Embodiment 8 Basically the same as Embodiment 1, except that:
  • the water-based two-component baking type automobile varnish improved in acid corrosion resistance of the present embodiment expressed by weight percentage, the water-based two-component baking type automobile varnish SA and ⁇ two components, group
  • the mass ratio between the tiller and the component ⁇ is 4:1, where:
  • composition of component A is: methyl methacrylate 27%, n-propyl acrylate 38%, vinyl acetate 8%, acrylic acid 10%, methacrylic acid- ⁇ -hydroxyethyl ester 16% and dodecyl mercaptan 1.0% ;
  • composition of the bismuth component is: 9% methyl methacrylate, 39% n-propyl acrylate, 9% vinyl acetate, 10% acrylic acid, Phthalic acid- ⁇ -hydroxyethyl ester 32% and dodecyl mercaptan 1.0%.
  • the preparation method of the aqueous two-component baking type automobile varnish improved in acid corrosion resistance of this embodiment is the same as that in the first embodiment.
  • the aqueous two-component baking type automobile varnish improved in acid corrosion resistance prepared by the above method of the present embodiment has a pencil hardness of 2 ⁇ , an impact strength of 50 kg, cm, an adhesion level of 1, and a flexibility of 1 mm. Gloss 113 (60°), excellent acid corrosion resistance. Use a 30% sulfuric acid solution as the acidic medium. The film should be immersed for at least 56 hours at 25 ° C without blistering.

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Abstract

提供了一种耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆及其制备方法。水性双组份烘烤型汽车罩光清漆由A、B两种组分组成,组分A和组分B均由甲基丙烯酸酯类单体、丙烯酸酯类单体、非丙烯酸酯类单体、丙烯酸类单体、含羟基的丙烯酸酯类单体和链转移剂组成;组分A和组分B分别将各种原料混合作为溶质,加入溶剂混合均匀得到溶液,然后加入引发剂并经溶液聚合反应,最后加入中和剂调整到所需中和度,分别得到水性丙烯酸树脂A和水性丙烯酸树脂B,最后将其所得两种物质进行混合,并加入交联剂后加水调整到所需黏度,得到产品。产品具有优异的综合性能,特别是具有良好的耐酸蚀性,并且原材料价格较低,是一种环保型水性罩光清漆。

Description

耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆及其制备方法 技术领域
本发明涉及一种水性涂料组合物,特别是涉及一种耐酸蚀性改善的水性双组份烘烤型 汽车罩光清漆及其制备方法。
背景技术
随着人们物质生活水平的不断提高, 罩光漆在各种产品 (如: 汽车、 塑料、 玻璃制品 等)得到了广泛的应用, 以提高产品的外观装饰效果及保护底漆用。 现有的罩光漆主要由 树脂成膜物和溶剂组成, 成膜物一般由聚酯树脂或丙烯酸树脂与氨基树脂交联固化而成, 丙烯酸树脂以其较好的耐候性得到广泛应用; 溶剂一般为挥发性有机溶剂。现有的罩光漆 主要存在以下缺点:
( 1 ) 大多数只能用于粗燥金属表面, 在塑料 (ABS、 PA、 PB、 PP、 PC, PVC等)、 玻 璃和表面光滑的金属合金基材上, 难以附着;
( 2 ) 漆膜的硬度和韧性很难兼顾, 硬度很难突破 3H, 韧性也很难突破 1;
( 3 ) 漆膜防刮擦性能差;
( 4) 漆膜耐溶剂性能、 耐水煮和耐人体汗液接触性能差;
( 5 )、 溶剂大多有毒害, 挥发在空气中污染空气和损害人类健康;
( 6 )、 喷涂施工难度大 (湿膜状态下, 不能重复施工);
( 7 )、 表面容易产生针孔、 鱼眼, 光滑平整度差;
( 8 )、 性价比低, 从而使生产成本较高, 造成推广、 销售和市场接受难。
总之, 现有的罩光漆存在适用范围小、 防刮擦性能差、 不环保及成本高的问题。 其中用于汽车车身的罩光清漆涂层是汽车车身的最终涂层,它影响整个汽车的外观装 饰性,要求具有良好的光泽度,同时该涂层暴露于空气中,接触到酸雨及其他空气污染物, 要求具有较好的耐酸蚀性。 目前轿车涂装多采用溶剂型罩光清漆, 虽说其性能优异, 但是 同时产生的大量挥发性有机物对环境造成污染,而目前市场上的环保型水性罩光清漆由于 生产成本较高且性能不及溶剂型罩光清漆而限制了应用。
发明内容
本发明的目的是针对现有汽车车身用罩光清漆存在的成本高、 不环保等缺陷, 提供一 种成本较低、 环保型的耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆及其制备方法。
为了解决上述问题, 本发明采用的技术方案是:
本发明提供一种耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆, 以重量百分含量表 示, 所述水性双组份烘烤型汽车罩光清漆由 A、 B两种组分组成, 组分 A和组分 B二者之 间的质量比为 1〜4:1, 其中:
A组分组成为: 甲基丙烯酸酯类单体 20〜30%, 丙烯酸酯类单体 35〜45%, 非丙烯酸 酯类单体 5〜: 15%, 丙烯酸类单体 5〜: 15%, 含羟基的丙烯酸酯类单体 10〜20%和链转移剂 0.5—1.5%;
B组分组成为: 甲基丙烯酸酯类单体 5〜: 15%, 丙烯酸酯类单体 35〜45%, 非丙烯酸 酯类单体 5〜: 15%, 丙烯酸类单体 5〜: 15%, 含羟基的丙烯酸酯类单体 25〜35%和链转移剂 0.5〜:! .5%。
根据上述的耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆,所述甲基丙烯酸酯类单 体为甲基丙烯酸甲酯、 甲基丙烯酸乙酯、 甲基丙烯酸异丙酯、 甲基丙烯酸异丁酯和甲基丙 烯酸叔丁酯中的任一种;
所述丙烯酸酯类单体为丙烯酸丁酯、 丙烯酸甲酯、 丙烯酸乙酯、 丙烯酸异丙酯、 丙烯 酸正丙酯、 丙烯酸 -2-乙基己酯和丙烯酸异丁酯中的任一种;
所述非丙烯酸酯类单体为苯乙烯或醋酸乙烯酯;
所述丙烯酸类单体为丙烯酸、 甲基丙烯酸或衣康酸;
所述含羟基的丙烯酸酯类单体为丙烯酸 -β-羟乙酯、 丙烯酸 -β-羟丙酯、 甲基丙烯酸 -β- 羟乙酯或甲基丙烯酸 -β-羟丙酯;
所述链转移剂为十二烷基硫醇、 四氯化碳、 正丁基硫醇、 特丁硫醇、 四溴化碳、 正丁 基硫醚、 异丙苯、 β-萘硫酚和四氧化碳中的任一种。
根据上述的耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆, Α组分组成为: 甲基丙 烯酸甲酯 20〜30%, 丙烯酸丁酯 35〜45%, 苯乙烯 5〜: 15%, 丙烯酸 5〜: 15%, 甲基丙烯酸 -β-羟乙酯 10〜20%和十二烷基硫醇 0.5〜: 1.5%;
Β组分组成为: 甲基丙烯酸甲酯 5〜: 15%, 丙烯酸丁酯 35〜45%, 苯乙烯 5〜: 15%, 丙 烯酸 5〜: 15%, 甲基丙烯酸 -β-羟乙酯 25〜35%和十二烷基硫醇 0.5〜: 1.5%。
根据上述的耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆, Α组分组成为: 甲基丙 烯酸甲酯 25%, 丙烯酸丁酯 40%, 苯乙烯 10%, 丙烯酸 9%, 甲基丙烯酸 -β-羟乙酯 15%和 十二烷基硫醇 1.0%;
Β组分组成为: 甲基丙烯酸甲酯 10%, 丙烯酸丁酯 40%, 苯乙烯 10%, 丙烯酸 9%, 甲 基丙烯酸 -β-羟乙酯 30%和十二烷基硫醇 1.0%。
一种上述耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆的制备方法, 所述制备方法 包括以下步骤:
a、首先按照上述耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆中的 Α组分组成称取 各种原料, 将称取的各种原料进行混合, 得到的混合物作为溶质, 将溶质溶解于溶剂中, 充分溶解后得到溶液, 所得溶液的质量百分浓度为 50〜70%; 然后在溶液中加入占溶质总 质量 1.4〜3%的引发剂混合均匀, 混合均匀后得到溶液 A; 将得到的溶液 A经常规溶液聚合 反应得到丙烯酸树脂 A; 然后降温至 50〜60°C, 加入中和剂, 调整丙烯酸树脂 A的中和度为 60〜: 100%, 得到水性丙烯酸树脂 A;
b、按照上述耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆中的 B组分组成称取各种 原料, 将称取的各种原料进行混合, 得到的混合物作为溶质, 将溶质溶解于溶剂中, 充分 溶解后得到溶液, 所得溶液的质量百分浓度为 50〜70%; 然后在溶液中加入占溶质总质量 0.3〜: 1.1%的引发剂混合均匀, 混合均匀后得到溶液 B; 将得到的溶液 B经常规溶液聚合反 应得到丙烯酸树脂 B;然后降温至 50〜60°C,加入中和剂,调整丙烯酸树脂 B的中和度为 60〜 100%, 得到水性丙烯酸树脂 B;
c、将步骤 a得到的水性丙烯酸树脂 A与步骤 b得到的水性丙烯酸树脂 B按照质量比为 1〜 4:1的比例进行混合, 混合均匀后得到混合水性丙烯酸树脂, 然后加入交联剂六甲氧甲基 三聚氰胺甲醛树脂, 混合水性丙烯酸树脂与交联剂二者加入的质量比为 2〜3:1, 最后加水 稀释至所需粘度,稀释到所需粘度后得到本发明产品耐酸蚀性改善的水性双组份烘烤型汽 车罩光清漆。
根据上述的耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆的制备方法,所述溶剂为 丙二醇甲醚、 异丙醇、 乙醇、 丙醇、 丁醇、 异丁醇、 仲丁醇、 叔丁醇、 1-乙氧基 -2-丙醇、 1-异丙氧基 -2-丙醇、 1-丙氧基 -2-丙醇和 1-丁氧基 -2-丙醇的任一种或任两种;
所述引发剂为偶氮二异丁腈、 偶氮二异庚腈、 过氧化苯甲酰、 过氧化二叔丁基、 过氧 化苯甲酸叔丁酯、 60%苯二甲酸二甲酯溶液和过氧化二异丁酰中的任一种;
所述中和剂为二甲基乙醇胺、 吗啉、 一乙胺、 二乙胺、三乙胺、 二乙基乙醇胺、 一乙 醇胺、 二乙醇胺、 三乙醇胺和二异丙醇胺中的任一种。
根据上述的耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆的制备方法,所述溶剂为 丙二醇甲醚和异丙醇的混合物, 丙二醇甲醚和异丙醇二者混合时的体积比为 1〜4:1;
所述引发剂为偶氮二异丁腈; 所述中和剂为二甲基乙醇胺。
根据上述的耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆的制备方法,所述溶液聚 合反应时控制反应温度为 80〜: 120°C, 反应时间为 6〜8h。
本发明组分 A的各种原料经混合反应得到数均分子量为 10000左右的水性丙烯酸树脂 A, 组分 B的各种原料经混合反应得到数均分子量为 20000左右的水性丙烯酸树脂 B, 水 性丙烯酸树脂 A和水性丙烯酸树脂 B混合并加入交联剂,树脂分子链上和交联剂发生反应 的基团为羟基, 根据交联聚合物材料结构与性能的原理, 树脂分子量高, 聚合物机械性能 好, 但是分子量太高, 其黏度也相应增大, 交联反应发生变得困难, 同时交联度高, 材料 的硬度高, 耐化学品性能好。本发明将水性丙烯酸树脂 A与水性丙烯酸树脂 B按照质量比 为 1〜4:1的比例进行混合, 丙烯酸树脂 B的分子量较高且分子链上发生交联反应的羟基 基团的数量比丙烯酸树脂 A的数量大一倍, 而它在混合树脂中所占比例较小, 这样就可以 使混合树脂黏度不至太大而影响交联反应的充分发生, 同时可以达到提高混合树脂的平均 分子量和漆膜的交联度的目的。 因此, 本发明最终形成的产品交联结构很致密, 使其制备 的产品获得优异的综合性能。
本发明的积极有益效果:
1、 本发明组分 A的各种原料经混合反应得到数均分子量为 10000左右的水性丙烯酸 树脂 A,组分 B的各种原料经混合反应得到数均分子量为 20000左右的水性丙烯酸树脂 B, 通过加入交联剂六甲氧甲基三聚氰胺甲醛树脂,数均分子量为 10000左右和数均分子量为 20000左右的两种水溶性丙烯酸树脂与交联剂发生交联反应, 这样最终形成的交联结构很 致密, 获得的涂膜具有优异的综合性能, 特别是具有良好的耐酸蚀性; 并且原材料价格较 低, 使其生产成本较低。
2、 采用本发明方法制备的耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆, 获得的 漆膜其铅笔硬度为 2H,冲击强度为 50kg'cm,附着力 1级,柔韧性 1mm,光泽度 113( 60° ); 并且耐酸蚀性尤其优异, 采用质量分数为 30%的硫酸溶液作为酸性介质, 涂膜在 25°C下 浸泡至少 56小时不起泡不发白。
3、 本发明采用的所有原料价格低廉, 并且容易得到, 使其制备本发明产品的生产成 本较低, 而且生产工艺简单。 因此, 本发明制备的产品耐酸蚀性改善的水性双组份烘烤型 汽车罩光清漆成本较低, 易于推广实施, 具有显著的经济效益。
4、 利用本发明技术方案制备耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆, 不会 产生的大量挥发性有机物对环境造成污染, 属于环保型水性罩光清漆。
具体实施方式:
以下结合实施例进一步阐释本发明, 但并不限制本发明的内容。
实施例 1:
本实施例耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆, 以重量百分含量表示, 所 述水性双组份烘烤型汽车罩光清漆 S A、 Β两种组分组成, 组分 Α和组分 Β二者之间的质 量比为 3:1, 其中:
A组分组成为: 甲基丙烯酸甲酯 25%, 丙烯酸丁酯 40%, 苯乙烯 10%, 丙烯酸 9%, 甲 基丙烯酸 -β-羟乙酯 15%和十二烷基硫醇 1.0%;
Β组分组成为: 甲基丙烯酸甲酯 10%, 丙烯酸丁酯 40%, 苯乙烯 10%, 丙烯酸 9%, 甲 基丙烯酸 -β-羟乙酯 30%和十二烷基硫醇 1.0%。
本实施例耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆的制备方法,所述制备方法 包括以下步骤:
a、首先按照上述本实施例耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆中的 Α组分 组成称取各种原料, 将称取的各种原料进行混合, 得到的混合物作为溶质, 将溶质溶解于 丙二醇甲醚和异丙醇的混合物溶剂中 (丙二醇甲醚和异丙醇二者混合时的体积比为 2:1), 充分溶解后得到溶液, 所得溶液的质量百分浓度为 60%; 然后在溶液中加入占溶质总质量 1.7%的引发剂偶氮二异丁腈混合均匀, 混合均匀后得到溶液 A; 将得到的溶液 A经常规溶液 聚合反应得到丙烯酸树脂 A (溶液聚合反应时控制反应温度为 80〜: 120°C,反应时间 6〜8h ); 然后降温至 50〜60°C, 加入中和剂二甲基乙醇胺, 调整树脂的中和度为 70%, 得到水性丙 烯酸树脂 A;
b、按照上述本实施例耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆中的 B组分组成 称取各种原料, 将称取的各种原料进行混合, 得到的混合物作为溶质, 将溶质溶解于丙二 醇甲醚和异丙醇的混合物溶剂中 (丙二醇甲醚和异丙醇二者混合时的体积比为 2:1), 充分 溶解后得到溶液, 所得溶液的质量百分浓度为 60%; 然后在溶液中加入占溶质总质量 0.5% 的引发剂偶氮二异丁腈混合均匀, 混合均匀后得到溶液 B; 将得到的溶液 B经常规溶液聚合 反应得到丙烯酸树脂 B (溶液聚合反应时控制反应温度为 80〜: 120°C, 反应时间 6〜8h ); 然 后降温至 50〜60°C, 加入中和剂, 调整树脂的中和度为 70%, 得到水性丙烯酸树脂 B; c 将步骤 a得到的水性丙烯酸树脂 A与步骤 b得到的水性丙烯酸树脂 B按照质量比为 3:1 的比例进行混合, 混合均匀后得到混合水性丙烯酸树脂, 然后加入交联剂六甲氧甲基三聚 氰胺甲醛树脂, 混合水性丙烯酸树脂与交联剂二者加入的质量比为 3:1, 最后加水稀释至 所需粘度,稀释到所需粘度后得到本实施例产品耐酸蚀性改善的水性双组份烘烤型汽车罩 光清漆。
实施例 2: 与实施例 1基本相同, 不同之处在于:
本实施例耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆, 以重量百分含量表示, 所 述水性双组份烘烤型汽车罩光清漆 S A、 Β两种组分组成, 组分 Α和组分 Β二者之间的质 量比为 4:1, 其中:
A组分组成为: 甲基丙烯酸甲酯 23%, 丙烯酸丁酯 45%, 苯乙烯 6.5%, 丙烯酸 15%, 甲基丙烯酸 -β-羟乙酯 10%和十二烷基硫醇 0.5%;
Β组分组成为: 甲基丙烯酸甲酯 15%, 丙烯酸丁酯 37%, 苯乙烯 15%, 丙烯酸 6%, 甲基丙烯酸 -β-羟乙酯 26.5%和十二烷基硫醇 0.5%。
本实施例耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆的制备方法, 与实施例 1 不同之处在于:
步骤 a 中: 将溶质溶解于丙二醇甲醚和异丙醇的混合物溶剂中 (丙二醇甲醚和异丙 醇二者混合时的体积比为 3:1), 充分溶解后得到溶液, 所得溶液的质量百分浓度为 70%; 然后在溶液中加入占溶质总质量 1.2%的引发剂过氧化苯甲酸叔丁酯混合均匀;将得到的溶 液经常规溶液聚合反应得到丙烯酸树脂 A (溶液聚合反应时控制反应温度为 80〜: 120°C, 反应时间 6〜8h ); 然后降温至 50〜60°C, 加入中和剂二异丙醇胺, 调整溶液的中和度为 60%; 得到水性丙烯酸树脂 A。
步骤 b 中: 将溶质溶解于丙二醇甲醚和异丙醇的混合物溶剂中 (丙二醇甲醚和异丙 醇二者混合时的体积比为 3:1), 充分溶解后得到溶液, 所得溶液的质量百分浓度为 70%; 然后在溶液中加入占溶质总质量 0.8%的引发剂过氧化苯甲酸叔丁酯混合均匀;将得到的溶 液经常规溶液聚合反应得到丙烯酸树脂 B (溶液聚合反应时控制反应温度为 80〜: 120°C, 反应时间 6〜8h ); 然后降温至 50〜60°C, 加入中和剂二异丙醇胺, 调整溶液的中和度为 60%; 得到水性丙烯酸树脂 B
步骤 c中:将步骤 a得到的水性丙烯酸树脂 A与步骤 b得到的水性丙烯酸树脂 B按照 质量比为 4:1的比例进行混合, 混合水性丙烯酸树脂与交联剂二者加入的质量比为 2:1。
实施例 3: 与实施例 1基本相同, 不同之处在于: 本实施例耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆, 以重量百分含量表示, 所 述水性双组份烘烤型汽车罩光清漆 S A、 Β两种组分组成, 组分 Α和组分 Β二者之间的质 量比为 2:1, 其中:
A组分组成为: 甲基丙烯酸甲酯 30%, 丙烯酸丁酯 35%, 苯乙烯 8.5%, 丙烯酸 5%, 甲基丙烯酸 -β-羟乙酯 20%和十二烷基硫醇 1.5%;
Β组分组成为: 甲基丙烯酸甲酯 5%, 丙烯酸丁酯 45%, 苯乙烯 5%, 丙烯酸 15%, 甲 基丙烯酸 -β-羟乙酯 28.5%和十二烷基硫醇 1.5%。
本实施例耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆的制备方法,与实施例 1不 同之处在于:
步骤 a中: 将溶质溶解于丙二醇甲醚和异丙醇的混合物溶剂中 (丙二醇甲醚和异丙醇 二者混合时的体积比为 4:1), 充分溶解后得到溶液, 所得溶液的质量百分浓度为 50%; 然 后在溶液中加入占溶质总质量 1.5%的引发剂偶氮二异庚腈混合均匀;将得到的溶液经常规 溶液聚合反应得到丙烯酸树脂 A (溶液聚合反应时控制反应温度为 80〜: 120°C, 反应时间 6〜8h); 然后降温至 50〜60°C, 加入中和剂二乙基乙醇胺, 调整溶液的中和度为 80%得 到水性丙烯酸树脂 A。
步骤 b中: 将溶质溶解于丙二醇甲醚和异丙醇的混合物溶剂中(丙二醇甲醚和异丙醇 二者混合时的体积比为 4:1), 充分溶解后得到溶液, 所得溶液的质量百分浓度为 50%; 然 后在溶液中加入占溶质总质量 1.0%的引发剂偶氮二异庚腈混合均匀;将得到的溶液经常规 溶液聚合反应得到丙烯酸树脂 B (溶液聚合反应时控制反应温度为 80〜: 120°C, 反应时间 6〜8h); 然后降温至 50〜60°C, 加入中和剂二乙基乙醇胺, 调整溶液的中和度为 80%, 得到水性丙烯酸树脂 B;
步骤 c中:将步骤 a得到的水性丙烯酸树脂 A与步骤 b得到的水性丙烯酸树脂 B按照 质量比为 2:1的比例进行混合, 再加入交联剂混合水性丙烯酸树脂与交联剂二者加入的质 实施例 4: 与实施例 1基本相同, 不同之处在于:
本实施例耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆, 以重量百分含量表示, 所 述水性双组份烘烤型汽车罩光清漆 S A、 Β两种组分组成, 组分 Α和组分 Β二者之间的质 量比为 1:1, 其中:
A组分组成为: 甲基丙烯酸甲酯 27%, 丙烯酸丁酯 38%, 苯乙烯 8%, 丙烯酸 10%, 甲 基丙烯酸 -β-羟乙酯 16%和十二烷基硫醇 1.0%;
Β组分组成为: 甲基丙烯酸甲酯 9%, 丙烯酸丁酯 39%, 苯乙烯 9%, 丙烯酸 10%, 甲 基丙烯酸 -β-羟乙酯 32%和十二烷基硫醇 1.0%。
本实施例耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆的制备方法与实施例 1 相 同。
实施例 5: 与实施例 1基本相同, 不同之处在于: 以重量百分含量表示, 所述水性双组份烘烤型汽车罩光清漆由 A、 B两种组分组成, 组分 A和组分 B二者之间的质量比为 3:1, 其中:
A组分组成为: 甲基丙烯酸乙酯 25%, 丙烯酸甲酯 40%, 醋酸乙烯酯 10%, 甲基丙烯 酸 9%, 丙烯酸羟乙酯 15%和正丁基硫醇 1.0%;
B组分组成为: 甲基丙烯酸乙酯 10%, 丙烯酸甲酯 40%, 醋酸乙烯酯 10%, 甲基丙烯 酸 9%, 丙烯酸羟乙酯 30%和正丁基硫醇 1.0%。
本实施例耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆的制备方法与实施例 1 相 同。
实施例 6: 与实施例 1基本相同, 不同之处在于:
本实施例耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆, 以重量百分含量表示, 所 述水性双组份烘烤型汽车罩光清漆 S A、 Β两种组分组成, 组分 Α和组分 Β二者之间的质 量比为 2:1, 其中:
A组分组成为: 甲基丙烯酸异丙酯 23%,丙烯酸乙酯 45%,苯乙烯 6.5%,衣康酸 15%, 丙烯酸羟丙酯 10%和正丁基硫醚 0.5%;
B组分组成为: 甲基丙烯酸异丙酯 15%, 丙烯酸乙酯 37%, 苯乙烯 15%, 衣康酸 6%, 丙烯酸羟丙酯 26.5%和正丁基硫醚 0.5%。
本实施例耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆的制备方法与实施例 1 相 同。
实施例 7: 与实施例 1基本相同, 不同之处在于:
本实施例耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆, 以重量百分含量表示, 所 述水性双组份烘烤型汽车罩光清漆 S A、 Β两种组分组成, 组分 Α和组分 Β二者之间的质 量比为 4:1, 其中:
A组分组成为: 甲基丙烯酸异丁酯 30%, 丙烯酸异丁酯 35%, 苯乙烯 8.5%, 丙烯酸 5%, 甲基丙烯酸 -β-羟丙酯 20%和异丙苯 1.5%;
Β组分组成为: 甲基丙烯酸异丁酯 5%,丙烯酸异丁酯 45%,苯乙烯 5%,丙烯酸 15%, 甲基丙烯酸 -β-羟丙酯 28.5%和异丙苯 1.5%。
本实施例耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆的制备方法与实施例 1 相 同。
实施例 8: 与实施例 1基本相同, 不同之处在于:
本实施例耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆, 以重量百分含量表示, 所 述水性双组份烘烤型汽车罩光清漆 S A、 Β两种组分组成, 组分 Α和组分 Β二者之间的质 量比为 4:1, 其中:
A组分组成为: 甲基丙烯酸甲酯 27%, 丙烯酸正丙酯 38%, 醋酸乙烯酯 8%, 丙烯酸 10%, 甲基丙烯酸 -β-羟乙酯 16%和十二烷基硫醇 1.0%;
Β组分组成为:甲基丙烯酸甲酯 9%,丙烯酸正丙酯 39%,醋酸乙烯酯 9%,丙烯酸 10%, 甲基丙烯酸 -β-羟乙酯 32%和十二烷基硫醇 1.0%。
本实施例耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆的制备方法与实施例 1 相 同。
采用本实施例上述方法制备的耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆,获得 的漆膜其铅笔硬度为 2Η, 冲击强度为 50kg,cm, 附着力 1级, 柔韧性 lmm, 光泽度 113 ( 60°), 耐酸蚀性尤其优异, 采用质量分数为 30%的硫酸溶液作为酸性介质, 涂膜在 25°C 下浸泡至少 56小时不起泡不发白。

Claims

权利要求书
1、 一种耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆, 其特征在于, 以 重量百分含量表示,所述水性双组份烘烤型汽车罩光清漆由 A、B两种组分组成, 组分 A和组分 B二者之间的质量比为 1〜4:1, 其中:
A组分组成为: 甲基丙烯酸酯类单体 20〜30%,丙烯酸酯类单体 35〜45%, 非丙烯酸酯类单体 5〜: 15%, 丙烯酸类单体 5〜: 15%, 含羟基的丙烯酸酯类单体 10〜20%和链转移剂 0.5〜1.5%;
B组分组成为: 甲基丙烯酸酯类单体 5〜: 15%, 丙烯酸酯类单体 35〜45%, 非丙烯酸酯类单体 5〜: 15%, 丙烯酸类单体 5〜: 15%, 含羟基的丙烯酸酯类单体 25〜35%和链转移剂 0.5〜: 1.5%。
2、根据权利要求 1所述的耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆, 其特征在于:
所述甲基丙烯酸酯类单体为甲基丙烯酸甲酯、 甲基丙烯酸乙酯、 甲基丙烯 酸异丙酯、 甲基丙烯酸异丁酯和甲基丙烯酸叔丁酯中的任一种;
所述丙烯酸酯类单体为丙烯酸丁酯、 丙烯酸甲酯、 丙烯酸乙酯、 丙烯酸异 丙酯、 丙烯酸正丙酯、 丙烯酸 -2-乙基己酯和丙烯酸异丁酯中的任一种;
所述非丙烯酸酯类单体为苯乙烯或醋酸乙烯酯;
所述丙烯酸类单体为丙烯酸、 甲基丙烯酸或衣康酸;
所述含羟基的丙烯酸酯类单体为丙烯酸 -β-羟乙酯、 丙烯酸 -β-羟丙酯、 甲基 丙烯酸 -β-羟乙酯或甲基丙烯酸 -β-羟丙酯;
链转移剂为十二烷基硫醇、 四氯化碳、正丁基硫醇、特丁硫醇、 四溴化碳、 正丁基硫醚、 异丙苯、 β-萘硫酚和四氧化碳中的任一种。
3、根据权利要求 1所述的耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆, 其特征在于, Α组分组成为: 甲基丙烯酸甲酯 20〜30%, 丙烯酸丁酯 35〜45%, 苯乙烯 5〜: 15%,丙烯酸 5〜: 15%, 甲基丙烯酸 -β-羟乙酯 10〜20%和十二烷基硫醇 0.5—1.5%;
Β组分组成为: 甲基丙烯酸甲酯 5〜: 15%,丙烯酸丁酯 35〜45%,苯乙烯 5〜 15%,丙烯酸 5〜: 15%,甲基丙烯酸 -β-羟乙酯 25〜35%和十二烷基硫醇 0.5〜: 1.5%。
4、根据权利要求 3所述的耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆, 其特征在于, Α组分组成为:甲基丙烯酸甲酯 25%,丙烯酸丁酯 40%,苯乙烯 10%, 丙烯酸 9%, 甲基丙烯酸 -β-羟乙酯 15%和十二烷基硫醇 1.0%;
Β组分组成为: 甲基丙烯酸甲酯 10%, 丙烯酸丁酯 40%, 苯乙烯 10%, 丙烯 酸 9%, 甲基丙烯酸 -β-羟乙酯 30%和十二烷基硫醇 1.0%。
5、一种权利要求 1所述的耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆 的制备方法, 其特征在于, 所述制备方法包括以下步骤:
a、首先按照权利要求 1所述的耐酸蚀性改善的水性双组份烘烤型汽车罩光清 漆中的 A组分组成称取各种原料, 将称取的各种原料进行混合, 得到的混合物作 为溶质, 将溶质溶解于溶剂中, 充分溶解后得到溶液, 所得溶液的质量百分浓度 为 50〜70%; 然后在溶液中加入占溶质总质量 1.4〜3%的引发剂混合均匀, 混合 均匀后得到溶液 A; 将得到的溶液 A经常规溶液聚合反应得到丙烯酸树脂 A; 然后 降温至 50〜60°C, 加入中和剂, 调整丙烯酸树脂 A的中和度为 60〜: 100%, 得到水 性丙烯酸树脂 A;
b、按照权利要求 1所述的耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆中 的 B组分组成称取各种原料, 将称取的各种原料进行混合, 得到的混合物作为溶 质,将溶质溶解于溶剂中,充分溶解后得到溶液,所得溶液的质量百分浓度为 50〜 70%; 然后在溶液中加入占溶质总质量 0.3〜: 1.1%的引发剂混合均匀, 混合均匀后 得到溶液 B; 将得到的溶液 B经常规溶液聚合反应得到丙烯酸树脂 B; 然后降温至 50〜60°C, 加入中和剂, 调整丙烯酸树脂 B的中和度为 60〜: 100%, 得到水性丙烯 酸树脂 B;
c 将步骤 a得到的水性丙烯酸树脂 A与步骤 b得到的水性丙烯酸树脂 B按照质 量比为:!〜 4:1的比例进行混合, 混合均匀后得到混合水性丙烯酸树脂, 然后加入 交联剂六甲氧甲基三聚氰胺甲醛树脂,混合水性丙烯酸树脂与交联剂二者加入的 质量比为 2〜3:1, 最后加水稀释至所需粘度, 稀释到所需粘度后得到本发明产品 耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆。
6、根据权利要求 5所述的耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆 的制备方法, 其特征在于:
所述溶剂为丙二醇甲醚、 异丙醇、 乙醇、 丙醇、 丁醇、 异丁醇、 仲丁醇、 叔 丁醇、 1-乙氧基 -2-丙醇、 1-异丙氧基 -2-丙醇、 1-丙氧基 -2-丙醇和 1-丁氧基 -2-丙醇 的任一种或任两种;
所述引发剂为偶氮二异丁腈、 偶氮二异庚腈、 过氧化苯甲酰、 过氧化二叔丁 基、 过氧化苯甲酸叔丁酯、 60%苯二甲酸二甲酯溶液和过氧化二异丁酰中的任一 种;
所述中和剂为二甲基乙醇胺、 吗啉、 一乙胺、 二乙胺、 三乙胺、 二乙基乙醇 胺、 一乙醇胺、 二乙醇胺、 三乙醇胺和二异丙醇胺中的任一种。
7、根据权利要求 6所述的耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆的 制备方法, 其特征在于:
所述溶剂为丙二醇甲醚和异丙醇的混合物,丙二醇甲醚和异丙醇二者混合时 的体积比为 1〜4:1;
所述引发剂为偶氮二异丁腈; 所述中和剂为二甲基乙醇胺。
8、根据权利要求 5所述的耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆 的制备方法, 其特征在于: 所述溶液聚合反应时控制反应温度为 80〜: 120°C, 反 应时间为 6〜8h。
PCT/CN2013/072422 2012-06-21 2013-03-11 耐酸蚀性改善的水性双组份烘烤型汽车罩光清漆及其制备方法 WO2013189192A1 (zh)

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