CN114806248B - Using method of fluorocarbon spray coating additive - Google Patents

Using method of fluorocarbon spray coating additive Download PDF

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Publication number
CN114806248B
CN114806248B CN202210397366.1A CN202210397366A CN114806248B CN 114806248 B CN114806248 B CN 114806248B CN 202210397366 A CN202210397366 A CN 202210397366A CN 114806248 B CN114806248 B CN 114806248B
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fluorocarbon
parts
spray coating
finish paint
coating additive
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CN114806248A (en
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黄长远
叶细发
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FUJIAN MINFA ALUMINIUM Inc
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FUJIAN MINFA ALUMINIUM Inc
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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
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/14Paints containing biocides, e.g. fungicides, insecticides or pesticides
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D3/00Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials
    • B05D3/02Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by baking
    • B05D3/0254After-treatment
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D7/00Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
    • B05D7/14Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials to metal, e.g. car bodies
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D7/00Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
    • B05D7/24Processes, 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D7/00Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
    • B05D7/50Multilayers
    • B05D7/56Three layers or more
    • B05D7/57Three layers or more the last layer being a clear coat
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D127/00Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers
    • C09D127/02Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
    • C09D127/12Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
    • C09D127/16Homopolymers or copolymers of vinylidene fluoride
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    • 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
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/08Anti-corrosive paints
    • C09D5/10Anti-corrosive paints containing metal dust
    • C09D5/103Anti-corrosive paints containing metal dust containing Al
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    • 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
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/45Anti-settling agents
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    • 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
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/47Levelling agents
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    • 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
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/60Additives non-macromolecular
    • C09D7/61Additives non-macromolecular inorganic
    • C09D7/62Additives non-macromolecular inorganic modified by treatment with other compounds
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    • 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
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/65Additives macromolecular
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D2202/00Metallic substrate
    • B05D2202/20Metallic substrate based on light metals
    • B05D2202/25Metallic substrate based on light metals based on Al
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D2506/00Halogenated polymers
    • B05D2506/10Fluorinated polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/02Elements
    • C08K3/08Metals
    • C08K2003/0806Silver
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/02Elements
    • C08K3/08Metals
    • C08K2003/0812Aluminium
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • C08K2003/2237Oxides; Hydroxides of metals of titanium
    • C08K2003/2241Titanium dioxide
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/32Phosphorus-containing compounds
    • C08K2003/321Phosphates
    • C08K2003/328Phosphates of heavy metals
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00Properties
    • C08L2201/08Stabilised against heat, light or radiation or oxydation

Abstract

The invention discloses a use method of a fluorocarbon spray coating additive, which comprises the following steps: s1, preparing a fluorocarbon spray coating additive: the additive comprises the following components in percentage by mass: 28-42% of low-density polyethylene, 10-18% of glutaric anhydride, 6-12% of chlorinated polyethylene, 30-45% of hydrophobic filler and 4-8% of silver ion antibacterial agent; s2, pretreatment: pre-treating the aluminum profile to form a passivation film on the surface of the aluminum profile; s3, spraying fluorocarbon primer; s4, spraying fluorocarbon finish paint: adding a fluorocarbon spray coating additive into the fluorocarbon finish paint formula, and performing electrostatic spray coating on the fluorocarbon finish paint to form a fluorocarbon finish paint layer; s5, spraying fluorocarbon varnish; s6, curing and baking. The method solves the problems of unstable quality and chromatic aberration of the product produced by the existing fluorocarbon spraying process.

Description

Using method of fluorocarbon spray coating additive
Technical Field
The invention relates to a use method of a fluorocarbon spray coating additive.
Background
The aluminum profile has the characteristics of small density, light weight, strong processability and plasticity and the like, and is widely applied to the field of building home furnishing. In order to improve the corrosion resistance and aging resistance of the aluminum profile and to improve the surface decoration effect of the aluminum profile, it is generally necessary to perform surface treatment. The aluminum profile surface treatment technology mainly comprises the following steps: powder spraying, fluorocarbon spraying, electrophoresis, anodic oxidation and wood grain transfer printing treatment.
The fluorine resin has a fluorine-carbon bond structure with shorter bond length and bond energy far higher than that of carbon-carbon and carbon-oxygen bonds, and can be closely arranged around the polymer, so that the fluorocarbon powder coating shows excellent weather resistance and is widely used as a protective decorative coating of aluminum profiles.
The fluorocarbon spraying process comprises the following steps: surface pretreatment-primer-topcoat- (varnish) -curing and baking. Patent application number CN202110580004.1 discloses a preparation method of a heat-insulating aluminum alloy section bar, which comprises the following steps: performing sand blasting treatment on the glue injection notch of the aluminum alloy substrate, and forming a sand surface on the surface of the glue injection notch; passivating and pre-treating the aluminum alloy substrate; the aluminum alloy base material is subjected to primer spraying treatment by PVDF fluorocarbon coating, and is dried; the aluminum alloy base material is sprayed with PVDF fluorocarbon paint and dried; solidifying the aluminum alloy base material; embossing a glue injection notch of an aluminum alloy substrate, and forming a concave tooth opening at the edge of the glue injection notch; injecting heat insulation glue into the glue injection notch, and drying and curing; and cutting the bridge of the aluminum alloy base material after glue injection to obtain a finished product. The preparation method can obtain the aluminum alloy section bar with good weather resistance and heat insulation effect, not only meets the performance requirements of longitudinal shearing resistance and the like, but also is suitable for the outdoor irradiation of high-strength sunlight. Patent application number CN201510029035.2 discloses an aluminum alloy profile and a manufacturing method thereof, comprising: the method comprises the following steps of (1) preprocessing an aluminum alloy profile base material; (2) Performing anodic oxidation treatment on the pretreated aluminum alloy section to form an oxide film on the surface of the aluminum alloy section; (3) Carrying out anode electrophoresis treatment on the aluminum alloy profile to form an electrophoresis paint film on the surface of the aluminum alloy profile; (4) curing and baking the aluminum alloy profile; (5) And spraying fluorocarbon paint on the surface of the aluminum alloy profile to form a fluorocarbon coating. The fluorocarbon coating at least comprises a fluorocarbon primer layer and a fluorocarbon top layer, and also comprises a fluorocarbon clear coat layer and a fluorocarbon middle coating. The production process of the manufacturing method is stable and easy to implement. The surface of the produced aluminum alloy section product has special composite film protective coating, has excellent corrosion resistance, weather resistance and other performances, can effectively resist ultraviolet rays, high humidity and corrosion damage of aggressive salt ions to the aluminum alloy section, and is particularly suitable for sea island and sea area buildings under marine climate.
However, the existing PVDF fluorocarbon coating has poor glossiness and gloss retention, and is difficult to produce a fluorocarbon paint film with high glossiness. The primer sprayed on the surface of the aluminum profile can enhance the protection of the base material, improve the adhesive force of the finish paint and ensure the color uniformity of the finish paint film. The finish paint can provide the required decorative color, so that the appearance meets the design requirement, and the surface of the aluminum profile is protected from being corroded by the external environment. The varnish has the function of protecting the finish paint coating, increasing the metallic luster of the color of the finish paint, and having more vivid appearance and bright luster. However, the adhesive force between the paint films of all layers and the adhesive force between the paint film and the aluminum profile are poor under the existing technological conditions, so that the paint film is easy to fall off and the due effect of the paint film cannot be exerted. In addition, the quality of the aluminum profile product sprayed by fluorocarbon is unstable, the color is uneven, and the color difference problem exists.
Disclosure of Invention
Therefore, aiming at the above, the invention provides a using method of the fluorocarbon spraying coating additive, which solves the problems of unstable quality and chromatic aberration of products produced by the existing fluorocarbon spraying technology.
In order to achieve the above purpose, the invention is realized by the following technical scheme:
the application method of the fluorocarbon spray coating additive comprises the following steps:
s1, preparing a fluorocarbon spray coating additive: the additive comprises the following components in percentage by mass: 28-42% of low-density polyethylene, 10-18% of glutaric anhydride, 6-12% of chlorinated polyethylene, 30-45% of hydrophobic filler and 4-8% of silver ion antibacterial agent;
s2, pretreatment: pre-treating the aluminum profile to form a passivation film on the surface of the aluminum profile;
s3, spraying fluorocarbon primer: uniformly spraying fluorocarbon primer on the surface of the aluminum profile by using a high-voltage electrostatic spray gun to form a fluorocarbon primer layer;
s4, spraying fluorocarbon finish paint: adding a fluorocarbon spray coating additive into the fluorocarbon finish paint formula, wherein the addition amount of the fluorocarbon spray coating additive is 3-6% of the mass of the fluorocarbon finish paint, stirring and mixing uniformly, and then uniformly spraying the fluorocarbon finish paint on the surface of the fluorocarbon primer layer by using a high-voltage electrostatic spray gun to form a fluorocarbon finish paint layer;
s5, spraying fluorocarbon varnish: uniformly spraying fluorocarbon varnish on the surface of the fluorocarbon finish paint layer by using a high-voltage electrostatic spray gun to form a fluorocarbon varnish layer;
s6, curing and baking: and (3) solidifying and baking the aluminum profile, and cooling to obtain the fluorocarbon powder spraying aluminum profile product.
The further improvement is that: the hydrophobic filler is formed by mixing talcum powder subjected to surface modification treatment and silicon dioxide according to the mass ratio of 1:0.8-2.
The further improvement is that: the silicon dioxide is subjected to surface modification treatment according to the following steps: the method comprises the following steps of (1) respectively weighing the following raw material components in parts by weight: 80-90 parts of silicon dioxide, 0.6-1.2 parts of perfluorooctyl triethoxysilane, 0.8-1.5 parts of benzoic acid and 0.1-0.3 part of triphenylphosphine; (2) Adding 1/3 weight of perfluorooctyl triethoxysilane into an ethanol solution, regulating the pH value by acetic acid to obtain weak acid perfluorooctyl triethoxysilane alcoholysis solution, adding silicon dioxide into the alcoholysis solution, stirring and reacting for 1-3h, reacting at 40-60 ℃, filtering and drying to obtain fluorosilane modified silicon dioxide; (3) 1/3 weight of perfluorooctyl triethoxysilane and benzoic acid are dissolved in toluene solvent, triphenylphosphine is added, and esterification reaction is carried out under inert gas atmosphere, so as to generate ester compounds; (4) Dissolving an ester compound and fluorosilane modified silicon dioxide in a toluene solvent, and reacting to generate an intermediate product; (5) The remaining perfluorooctyl triethoxysilane is reacted with the intermediate to yield hydrophobically modified silica.
The further improvement is that: the temperature of the esterification reaction is 80-100 ℃ and the reaction time is 3-6h.
The further improvement is that: the reaction temperature of the step (4) is 85-95 ℃ and the reaction time is 40-60min.
The further improvement is that: the reaction temperature in the step (5) is 90-105 ℃ and the reaction time is 20-40min.
The further improvement is that: the fluorocarbon primer comprises the following components in parts by weight: 10-18 parts of hydroxy acrylic resin, 18-28 parts of PVDF fluorocarbon resin, 8-15 parts of polyester resin, 22-32 parts of propylene glycol methyl ether acetate, 12-20 parts of butyl acetate, 15-25 parts of barium sulfate, 0.8-2 parts of dispersing agent and 0.5-1.5 parts of flatting agent.
The further improvement is that: the fluorocarbon finish paint comprises the following components in parts by weight: 10-18 parts of hydroxy acrylic resin, 25-35 parts of PVDF fluorocarbon resin, 22-32 parts of propylene glycol methyl ether acetate, 12-20 parts of butyl acetate, 6-10 parts of aluminum powder, 0.5-0.8 part of dispersing agent and 0.2-0.4 part of leveling agent.
The further improvement is that: the fluorocarbon varnish comprises the following components in parts by weight: 10-18 parts of hydroxy acrylic resin, 30-40 parts of PVDF fluorocarbon resin, 22-32 parts of propylene glycol methyl ether acetate, 12-20 parts of butyl acetate, 0.3-0.6 part of flatting agent, 0.2-0.4 part of ultraviolet light absorber and 0.1-0.3 part of light stabilizer.
The further improvement is that: and S6, curing and baking at 220-240 ℃ for 15-30min.
By adopting the technical scheme, the invention has the beneficial effects that:
the lamellar interlayer structure of the talcum powder can effectively improve the leveling property of the paint, fill gaps among aluminum powder, reduce the defects of the coating and improve the gloss retention of the coating; but also can prolong the diffusion path of corrosive medium, thereby improving the weather resistance of the coating film. Talc having a high aspect ratio also imparts higher impact resistance and fracture toughness to the coating film when the coating film is cured. Therefore, talcum powder in the additive is added into fluorocarbon finish paint, so that excellent gloss retention and leveling property can be provided for the coating film, and the impact resistance and weather resistance of the coating film can be improved.
The molecular structure of the perfluoro octyl triethoxy silane as the silane coupling agent contains a large number of fluorine-containing groups, and the silicon dioxide is modified by perfluoro octyl triethoxy silane, so that the particle surface of the silicon dioxide is provided with hydrophobic groups, thereby endowing the surface with superhydrophobicity. When the powder coating is cured at high temperature, white spots are easy to appear on the surface of the powder coating due to water absorption of the coating. The ethoxy in the perfluorooctyl triethoxy silane molecular structure and the active silicon hydroxyl on the surface of the silicon dioxide are subjected to coupling reaction, so that the silicon dioxide can be promoted to be dispersed in an organic system. However, it was found in the course of the study that the modified silica obtained by using perfluorooctyl triethoxysilane alone has poor compatibility with organic systems. In order to solve the problems, the invention adopts the following method: firstly, under the catalysis of triphenylphosphine, benzoic acid and perfluorooctyl triethoxysilane undergo esterification reaction to generate an ester compound; secondly, the ester compound and the fluorosilane modified silicon dioxide undergo a coupling reaction, and the functional group of the ester compound is grafted on the surface of the silicon dioxide (namely an intermediate product is formed), so that the compatibility and the dispersibility of the silicon dioxide in an organic system are improved; finally, the perfluoro octyl triethoxy silane is utilized to carry out coupling reaction with active silicon hydroxyl on the surface of the intermediate product, so that the functional group of the ester compound is firmly coated and fixed on the surface of the silicon dioxide, the silicon dioxide is not easy to fall off, and the compatible dispersion effect of the silicon dioxide in an organic system is affected.
The aluminum powder can be orderly arranged in the film forming process, and the gloss, texture and color uniformity of the coating film are directly affected. The low-density polyethylene in the additive has high shrinkage, and can enable a paint film to shrink rapidly in the curing process of curing, prevent aluminum powder from moving up and down in the paint film and assist the aluminum powder to be arranged horizontally and directionally. The aluminum powder has high specific gravity and is easy to sink, and the silicon dioxide in the additive can have good anti-sinking effect. The existing fluorocarbon powder coating only has excellent weather resistance, and the silver ion antibacterial agent is added to endow the paint film with antibacterial property to inhibit the breeding of microorganisms on the surface of the aluminum profile. The chlorinated polyethylene contains chlorine atoms with strong polarity, and the chlorine atoms are added into the fluorocarbon finish paint to use the strong polarity, so that the bonding force between the chlorinated polyethylene and the fluorocarbon primer and the fluorocarbon varnish can be enhanced. The compactness of the paint film can be improved by adding glutaric anhydride.
Furthermore, the film forming substance adopted by the fluorocarbon primer comprises hydroxy acrylic resin and polyester resin besides PVDF fluorocarbon resin, and the combination of the above components is matched with each other, so that the fluorocarbon primer can be firmly attached to the surface of the passivation film, and the adhesive force of a fluorocarbon paint film and an aluminum profile is improved. In addition, hydroxyl functional groups of the hydroxyl acrylic resin in the fluorocarbon primer can be subjected to crosslinking reaction with glutaric anhydride in the fluorocarbon finish paint, so that the bonding strength between the fluorocarbon primer and the fluorocarbon finish paint is improved.
Detailed Description
The following describes embodiments of the present invention in detail with reference to specific examples, so as to solve the technical problem by applying the technical means to the present invention, and the implementation process for achieving the technical effect can be fully understood and implemented accordingly.
Unless otherwise indicated, the technical means employed in the examples are conventional means well known to those skilled in the art, and the reagents and products employed are also commercially available. The sources of the reagents used, the trade names and the members of the list of constituents which are necessary are all indicated at the first occurrence.
Example 1
The application method of the fluorocarbon spray coating additive comprises the following steps:
s1, preparing a fluorocarbon spray coating additive: the additive comprises the following components in percentage by mass: 28% of low-density polyethylene, 18% of glutaric anhydride, 6% of chlorinated polyethylene, 44% of hydrophobic filler and 4% of silver ion antibacterial agent; the silver ion antibacterial agent is formed by mixing any one or more than two of zirconium phosphate silver-carrying, titanium dioxide silver-carrying and zeolite silver-carrying according to any ratio, and the titanium dioxide silver-carrying antibacterial agent is selected in the embodiment;
the hydrophobic filler is formed by mixing talcum powder subjected to surface modification treatment and silicon dioxide according to the mass ratio of 1:1.5, wherein the silicon dioxide is subjected to surface modification treatment according to the following steps: the method comprises the following steps of (1) respectively weighing the following raw material components in parts by weight: 80 parts of silicon dioxide, 0.6 part of perfluorooctyl triethoxysilane, 0.8 part of benzoic acid and 0.1 part of triphenylphosphine; (2) Adding 1/3 weight of perfluorooctyl triethoxysilane into an ethanol solution, regulating the pH value by acetic acid to obtain weak acid perfluorooctyl triethoxysilane alcoholysis solution, adding silicon dioxide into the alcoholysis solution, stirring for reaction for 3 hours, reacting at 40 ℃, filtering and drying to obtain fluorosilane modified silicon dioxide; (3) 1/3 weight of perfluorooctyl triethoxysilane and benzoic acid are dissolved in toluene solvent, triphenylphosphine is added, esterification reaction is carried out under inert gas atmosphere, the reaction temperature is 80 ℃, the reaction time is 6 hours, and ester compounds are generated; (4) Dissolving an ester compound and fluorosilane modified silicon dioxide in a toluene solvent, and reacting at the temperature of 85 ℃ for 60min to generate an intermediate product; (5) Reacting the rest perfluorooctyl triethoxysilane with the intermediate product at 90 ℃ for 40min to obtain hydrophobically modified silica;
the surface modification treatment of talcum powder is that talcum powder is put into alcoholysis liquid of gamma- (2, 3-epoxypropoxy) propyl trimethoxy silane, then the temperature is raised to 50 ℃, stirring reaction is carried out for 80min, filtration and drying are carried out, and the addition amount of gamma- (2, 3-epoxypropoxy) propyl trimethoxy silane is 2% of the mass of talcum powder;
s2, pretreatment: the method comprises the following steps of performing pretreatment on the aluminum profile to form a passivation film on the surface of the aluminum profile, wherein the pretreatment is common knowledge in the field and comprises the working procedures of degreasing, water-based and passivation;
s3, spraying fluorocarbon primer: uniformly spraying fluorocarbon primer on the surface of the aluminum profile by using a high-voltage electrostatic spray gun to form a fluorocarbon primer layer, wherein the fluorocarbon primer comprises the following components in parts by weight: 10 parts of hydroxy acrylic resin, 18 parts of PVDF fluorocarbon resin, 8 parts of polyester resin, 22 parts of propylene glycol methyl ether acetate, 12 parts of butyl acetate, 15 parts of barium sulfate, 0.8 part of dispersing agent and 0.5 part of flatting agent;
s4, spraying fluorocarbon finish paint: adding a fluorocarbon spray coating additive into a fluorocarbon finish paint formula, wherein the addition amount of the fluorocarbon spray coating additive is 3% of the mass of the fluorocarbon finish paint, and the fluorocarbon finish paint comprises the following components in parts by weight: 10 parts of hydroxy acrylic resin, 25 parts of PVDF fluorocarbon resin, 22 parts of propylene glycol methyl ether acetate, 12 parts of butyl acetate, 6 parts of aluminum powder, 0.5 part of dispersing agent and 0.2 part of flatting agent, and uniformly stirring and mixing, and then uniformly spraying fluorocarbon finish paint on the surface of the fluorocarbon primer layer by using a high-voltage electrostatic spray gun to form a fluorocarbon finish paint layer;
s5, spraying fluorocarbon varnish: uniformly spraying fluorocarbon varnish on the surface of the fluorocarbon finish paint layer by using a high-voltage electrostatic spray gun to form a fluorocarbon varnish layer, wherein the fluorocarbon varnish comprises the following components in parts by weight: 10 parts of hydroxy acrylic resin, 30 parts of PVDF fluorocarbon resin, 22 parts of propylene glycol methyl ether acetate, 12 parts of butyl acetate, 0.3 part of flatting agent, 0.2 part of ultraviolet light absorber and 0.1 part of light stabilizer;
s6, curing and baking: and (3) solidifying and baking the aluminum profile, and cooling to obtain the fluorocarbon powder spraying aluminum profile product. And S6, curing and baking at 220 ℃ for 30min.
Product performance detection is carried out on the aluminum profile of the embodiment, and the detection results are as follows: the paint film has uniform color and smooth and flat appearance; dry/wet adhesion (cross-hatch) was all grade 0; the 4000h xenon lamp irradiation accelerated aging test does not generate chalking phenomenon; the light retention rate of QUVB accelerated aging for 2000 hours is 95.2%.
Example 2
The application method of the fluorocarbon spray coating additive comprises the following steps:
s1, preparing a fluorocarbon spray coating additive: the additive comprises the following components in percentage by mass: 34% of low-density polyethylene, 14% of glutaric anhydride, 12% of chlorinated polyethylene, 34% of hydrophobic filler and 6% of silver-carrying antibacterial agent of zirconium phosphate;
the hydrophobic filler is formed by mixing talcum powder subjected to surface modification treatment and silicon dioxide according to a mass ratio of 1:2, wherein the silicon dioxide is subjected to surface modification treatment according to the following steps: the method comprises the following steps of (1) respectively weighing the following raw material components in parts by weight: 85 parts of silicon dioxide, 0.9 part of perfluorooctyl triethoxysilane, 1.2 parts of benzoic acid and 0.2 part of triphenylphosphine; (2) Adding 1/3 weight of perfluorooctyl triethoxysilane into an ethanol solution, regulating the pH value by acetic acid to obtain weak acid perfluorooctyl triethoxysilane alcoholysis solution, adding silicon dioxide into the alcoholysis solution, stirring and reacting for 2 hours, wherein the reaction temperature is 50 ℃, filtering and drying to obtain fluorosilane modified silicon dioxide; (3) 1/3 weight of perfluorooctyl triethoxysilane and benzoic acid are dissolved in toluene solvent, triphenylphosphine is added, esterification reaction is carried out under inert gas atmosphere, the reaction temperature is 90 ℃, the reaction time is 4 hours, and ester compounds are generated; (4) Dissolving an ester compound and fluorosilane modified silicon dioxide in a toluene solvent, and reacting at 90 ℃ for 50min to generate an intermediate product; (5) Reacting the rest perfluorooctyl triethoxysilane with the intermediate product at a reaction temperature of 100 ℃ for 30min to obtain hydrophobically modified silica;
the surface modification treatment of talcum powder is that talcum powder is put into alcoholysis liquid of gamma- (2, 3-epoxypropoxy) propyl trimethoxy silane, then the temperature is raised to 40 ℃, stirring reaction is carried out for 100min, filtration and drying are carried out, and the addition amount of gamma- (2, 3-epoxypropoxy) propyl trimethoxy silane is 3% of the mass of talcum powder;
s2, pretreatment: pre-treating the aluminum profile to form a passivation film on the surface of the aluminum profile;
s3, spraying fluorocarbon primer: uniformly spraying fluorocarbon primer on the surface of the aluminum profile by using a high-voltage electrostatic spray gun to form a fluorocarbon primer layer, wherein the fluorocarbon primer comprises the following components in parts by weight: 15 parts of hydroxy acrylic resin, 24 parts of PVDF fluorocarbon resin, 12 parts of polyester resin, 28 parts of propylene glycol methyl ether acetate, 16 parts of butyl acetate, 20 parts of barium sulfate, 1.5 parts of dispersing agent and 1 part of flatting agent;
s4, spraying fluorocarbon finish paint: the fluorocarbon paint additive is added into a fluorocarbon finish paint formula, the addition amount of the fluorocarbon paint additive is 5% of the mass of the fluorocarbon finish paint, and the fluorocarbon finish paint comprises the following components in parts by weight: 14 parts of hydroxy acrylic resin, 30 parts of PVDF fluorocarbon resin, 27 parts of propylene glycol methyl ether acetate, 16 parts of butyl acetate, 8 parts of aluminum powder, 0.6 part of dispersing agent and 0.3 part of flatting agent, stirring and mixing uniformly, and then uniformly spraying fluorocarbon finish paint on the surface of the fluorocarbon primer layer by using a high-voltage electrostatic spray gun to form a fluorocarbon finish paint layer;
s5, spraying fluorocarbon varnish: uniformly spraying fluorocarbon varnish on the surface of the fluorocarbon finish paint layer by using a high-voltage electrostatic spray gun to form a fluorocarbon varnish layer, wherein the fluorocarbon varnish comprises the following components in parts by weight: 14 parts of hydroxy acrylic resin, 35 parts of PVDF fluorocarbon resin, 27 parts of propylene glycol methyl ether acetate, 16 parts of butyl acetate, 0.5 part of flatting agent, 0.3 part of ultraviolet light absorber and 0.2 part of light stabilizer;
s6, curing and baking: and (3) solidifying and baking the aluminum profile, and cooling to obtain the fluorocarbon powder spraying aluminum profile product. And S6, curing and baking at 230 ℃ for 20min.
Product performance detection is carried out on the aluminum profile of the embodiment, and the detection results are as follows: the paint film has uniform color and smooth and flat appearance; dry/wet adhesion (cross-hatch) was all grade 0; the 4000h xenon lamp irradiation accelerated aging test does not generate chalking phenomenon; the light retention rate of QUVB accelerated aging for 2000 hours is 96.5%.
Example 3
The application method of the fluorocarbon spray coating additive comprises the following steps:
s1, preparing a fluorocarbon spray coating additive: the additive comprises the following components in percentage by mass: 42% of low-density polyethylene, 10% of glutaric anhydride, 9% of chlorinated polyethylene, 31% of hydrophobic filler and 8% of zeolite silver-carrying antibacterial agent;
the hydrophobic filler is formed by mixing talcum powder subjected to surface modification treatment and silicon dioxide according to a mass ratio of 1:1, wherein the silicon dioxide is subjected to surface modification treatment according to the following steps: the method comprises the following steps of (1) respectively weighing the following raw material components in parts by weight: 90 parts of silicon dioxide, 1.2 parts of perfluorooctyl triethoxysilane, 1.5 parts of benzoic acid and 0.3 part of triphenylphosphine; (2) Adding 1/3 weight of perfluorooctyl triethoxysilane into an ethanol solution, regulating the pH value by acetic acid to obtain weak acid perfluorooctyl triethoxysilane alcoholysis solution, adding silicon dioxide into the alcoholysis solution, stirring and reacting for 1h, wherein the reaction temperature is 60 ℃, filtering and drying to obtain fluorosilane modified silicon dioxide; (3) Dissolving 1/3 weight of perfluorooctyl triethoxysilane and benzoic acid in a toluene solvent, adding triphenylphosphine, and carrying out esterification reaction in an inert gas atmosphere at a reaction temperature of 100 ℃ for 3 hours to obtain an ester compound; (4) Dissolving an ester compound and fluorosilane modified silicon dioxide in a toluene solvent, and reacting at 95 ℃ for 40min to generate an intermediate product; (5) Reacting the rest perfluorooctyl triethoxysilane with the intermediate product at 105 ℃ for 20min to obtain hydrophobically modified silica;
the surface modification treatment of talcum powder is that talcum powder is put into alcoholysis liquid of gamma- (2, 3-epoxypropoxy) propyl trimethoxy silane, then the temperature is raised to 60 ℃, stirring reaction is carried out for 60min, filtration and drying are carried out, and the addition amount of gamma- (2, 3-epoxypropoxy) propyl trimethoxy silane is 4% of the mass of talcum powder;
s2, pretreatment: pre-treating the aluminum profile to form a passivation film on the surface of the aluminum profile;
s3, spraying fluorocarbon primer: uniformly spraying fluorocarbon primer on the surface of the aluminum profile by using a high-voltage electrostatic spray gun to form a fluorocarbon primer layer, wherein the fluorocarbon primer comprises the following components in parts by weight: 18 parts of hydroxy acrylic resin, 28 parts of PVDF fluorocarbon resin, 15 parts of polyester resin, 32 parts of propylene glycol methyl ether acetate, 20 parts of butyl acetate, 25 parts of barium sulfate, 2 parts of dispersing agent and 1.5 parts of flatting agent;
s4, spraying fluorocarbon finish paint: the fluorocarbon paint additive is added into a fluorocarbon finish paint formula, the addition amount of the fluorocarbon paint additive is 6% of the mass of the fluorocarbon finish paint, and the fluorocarbon finish paint comprises the following components in parts by weight: 18 parts of hydroxy acrylic resin, 35 parts of PVDF fluorocarbon resin, 32 parts of propylene glycol methyl ether acetate, 20 parts of butyl acetate, 10 parts of aluminum powder, 0.8 part of dispersing agent and 0.4 part of flatting agent, and uniformly stirring and mixing, and then uniformly spraying fluorocarbon finish paint on the surface of the fluorocarbon primer layer by using a high-voltage electrostatic spray gun to form a fluorocarbon finish paint layer;
s5, spraying fluorocarbon varnish: uniformly spraying fluorocarbon varnish on the surface of the fluorocarbon finish paint layer by using a high-voltage electrostatic spray gun to form a fluorocarbon varnish layer, wherein the fluorocarbon varnish comprises the following components in parts by weight: 18 parts of hydroxy acrylic resin, 40 parts of PVDF fluorocarbon resin, 32 parts of propylene glycol methyl ether acetate, 20 parts of butyl acetate, 6 parts of flatting agent, 0.4 part of ultraviolet light absorber and 0.3 part of light stabilizer;
s6, curing and baking: and (3) solidifying and baking the aluminum profile, and cooling to obtain the fluorocarbon powder spraying aluminum profile product. And S6, curing and baking at 240 ℃ for 15min.
Product performance detection is carried out on the aluminum profile of the embodiment, and the detection results are as follows: the paint film has uniform color and smooth and flat appearance; dry/wet adhesion (cross-hatch) was all grade 0; the 4000h xenon lamp irradiation accelerated aging test does not generate chalking phenomenon; the light retention rate of QUVB accelerated aging for 2000 hours is 96.0%.
Comparative example 1
The difference from example 1 is that: step S1 is omitted, namely fluorocarbon paint additive is not added into the fluorocarbon finish paint.
The aluminum profile of the comparative example was subjected to product performance detection with the following detection results: the paint film has obvious color difference and slight orange-peel appearance; dry adhesion (cross-hatch) is grade 1 and wet adhesion (cross-hatch) is grade 2; after the xenon lamp irradiates an accelerated aging test for 3000 hours, starting to generate a chalking phenomenon; the light retention rate of QUVB accelerated aging for 2000 hours is 71.4%.
Comparative example 2
The difference from example 1 is that: the fluorocarbon spray coating additive does not contain talcum powder.
The aluminum profile of the comparative example was subjected to product performance detection with the following detection results: dry/wet adhesion (cross-hatch) was all grade 0; after 3500h of the xenon lamp irradiation accelerated aging test, starting to generate chalking phenomenon; the light retention rate of QUVB accelerated aging for 2000 hours is 84.7%.
Comparative example 3
The difference from example 1 is that: the fluorocarbon spray coating additive does not contain low density polyethylene.
The aluminum profile of the comparative example was subjected to product performance detection with the following detection results: the paint film has obvious color difference and slight orange-peel appearance.
Comparative example 4
The difference from example 1 is that: the fluorocarbon spray coating additive does not contain glutaric anhydride.
The aluminum profile of the comparative example was subjected to product performance detection with the following detection results: the dry/wet adhesion (cross-hatch) was all grade 1.
Comparative example 5
The difference from example 1 is that: the fluorocarbon spray coating additive does not contain chlorinated polyethylene.
The aluminum profile of the comparative example was subjected to product performance detection with the following detection results: dry/wet adhesion (cross-hatch) was all grade 1; after 3500h of the xenon lamp irradiation accelerated aging test, the chalking phenomenon starts to occur.
The above description is illustrative of the embodiments using the present teachings, and is not intended to limit the scope of the present teachings to any particular modification or variation of the present teachings by those skilled in the art.

Claims (8)

1. The application method of the fluorocarbon spray coating additive is characterized by comprising the following steps of: the method comprises the following steps:
s1, preparing a fluorocarbon spray coating additive: the additive comprises the following components in percentage by mass: 28-42% of low-density polyethylene, 10-18% of glutaric anhydride, 6-12% of chlorinated polyethylene, 30-45% of hydrophobic filler and 4-8% of silver ion antibacterial agent, wherein the hydrophobic filler is formed by mixing talcum powder subjected to surface modification treatment and silicon dioxide according to the mass ratio of 1:0.8-2, and the silicon dioxide is subjected to surface modification treatment according to the following steps: the method comprises the following steps of (1) respectively weighing the following raw material components in parts by weight: 80-90 parts of silicon dioxide, 0.6-1.2 parts of perfluorooctyl triethoxysilane, 0.8-1.5 parts of benzoic acid and 0.1-0.3 part of triphenylphosphine; (2) Adding 1/3 weight of perfluorooctyl triethoxysilane into an ethanol solution, regulating the pH value by acetic acid to obtain weak acid perfluorooctyl triethoxysilane alcoholysis solution, adding silicon dioxide into the alcoholysis solution, stirring and reacting for 1-3h, reacting at 40-60 ℃, filtering and drying to obtain fluorosilane modified silicon dioxide; (3) 1/3 weight of perfluorooctyl triethoxysilane and benzoic acid are dissolved in toluene solvent, triphenylphosphine is added, and esterification reaction is carried out under inert gas atmosphere, so as to generate ester compounds; (4) Dissolving an ester compound and fluorosilane modified silicon dioxide in a toluene solvent, and reacting to generate an intermediate product; (5) Reacting the rest perfluorooctyl triethoxysilane with the intermediate product to obtain hydrophobically modified silica;
s2, pretreatment: pre-treating the aluminum profile to form a passivation film on the surface of the aluminum profile;
s3, spraying fluorocarbon primer: uniformly spraying fluorocarbon primer on the surface of the aluminum profile by using a high-voltage electrostatic spray gun to form a fluorocarbon primer layer;
s4, spraying fluorocarbon finish paint: adding a fluorocarbon spray coating additive into the fluorocarbon finish paint formula, wherein the addition amount of the fluorocarbon spray coating additive is 3-6% of the mass of the fluorocarbon finish paint, stirring and mixing uniformly, and then uniformly spraying the fluorocarbon finish paint on the surface of the fluorocarbon primer layer by using a high-voltage electrostatic spray gun to form a fluorocarbon finish paint layer;
s5, spraying fluorocarbon varnish: uniformly spraying fluorocarbon varnish on the surface of the fluorocarbon finish paint layer by using a high-voltage electrostatic spray gun to form a fluorocarbon varnish layer;
s6, curing and baking: and (3) solidifying and baking the aluminum profile, and cooling to obtain the fluorocarbon powder spraying aluminum profile product.
2. The method of using a fluorocarbon spray coating additive as set forth in claim 1, wherein: the temperature of the esterification reaction is 80-100 ℃ and the reaction time is 3-6h.
3. The method of using a fluorocarbon spray coating additive as set forth in claim 1, wherein: the reaction temperature of the step (4) is 85-95 ℃ and the reaction time is 40-60min.
4. The method of using a fluorocarbon spray coating additive as set forth in claim 1, wherein: the reaction temperature in the step (5) is 90-105 ℃ and the reaction time is 20-40min.
5. The method of using a fluorocarbon spray coating additive as set forth in claim 1, wherein: the fluorocarbon primer comprises the following components in parts by weight: 10-18 parts of hydroxy acrylic resin, 18-28 parts of PVDF fluorocarbon resin, 8-15 parts of polyester resin, 22-32 parts of propylene glycol methyl ether acetate, 12-20 parts of butyl acetate, 15-25 parts of barium sulfate, 0.8-2 parts of dispersing agent and 0.5-1.5 parts of flatting agent.
6. The method of using a fluorocarbon spray coating additive as set forth in claim 1, wherein: the fluorocarbon finish paint comprises the following components in parts by weight: 10-18 parts of hydroxy acrylic resin, 25-35 parts of PVDF fluorocarbon resin, 22-32 parts of propylene glycol methyl ether acetate, 12-20 parts of butyl acetate, 6-10 parts of aluminum powder, 0.5-0.8 part of dispersing agent and 0.2-0.4 part of leveling agent.
7. The method of using a fluorocarbon spray coating additive as set forth in claim 1, wherein: the fluorocarbon varnish comprises the following components in parts by weight: 10-18 parts of hydroxy acrylic resin, 30-40 parts of PVDF fluorocarbon resin, 22-32 parts of propylene glycol methyl ether acetate, 12-20 parts of butyl acetate, 0.3-0.6 part of flatting agent, 0.2-0.4 part of ultraviolet light absorber and 0.1-0.3 part of light stabilizer.
8. The method of using a fluorocarbon spray coating additive as set forth in claim 1, wherein: and S6, curing and baking at 220-240 ℃ for 15-30min.
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