[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

CN113512341A - Graphene oxide/epoxy vinyl ester resin heavy-duty anti-corrosion solvent-free composite coating and preparation method and application thereof - Google Patents

Graphene oxide/epoxy vinyl ester resin heavy-duty anti-corrosion solvent-free composite coating and preparation method and application thereof Download PDF

Info

Publication number
CN113512341A
CN113512341A CN202110878510.9A CN202110878510A CN113512341A CN 113512341 A CN113512341 A CN 113512341A CN 202110878510 A CN202110878510 A CN 202110878510A CN 113512341 A CN113512341 A CN 113512341A
Authority
CN
China
Prior art keywords
graphene oxide
solvent
vinyl ester
composite coating
ester resin
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN202110878510.9A
Other languages
Chinese (zh)
Other versions
CN113512341B (en
Inventor
杨卓鸿
李贵东
杨绍恒
方亨
刘继强
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Guangdong Sanqiu Optical Solid Materials Co ltd
South China Agricultural University
Original Assignee
Guangdong Sanqiu Optical Solid Materials Co ltd
South China Agricultural University
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Guangdong Sanqiu Optical Solid Materials Co ltd, South China Agricultural University filed Critical Guangdong Sanqiu Optical Solid Materials Co ltd
Priority to CN202110878510.9A priority Critical patent/CN113512341B/en
Publication of CN113512341A publication Critical patent/CN113512341A/en
Application granted granted Critical
Publication of CN113512341B publication Critical patent/CN113512341B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D163/00Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
    • C09D163/10Epoxy resins modified by unsaturated compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/14Polycondensates modified by chemical after-treatment
    • C08G59/1433Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds
    • C08G59/1438Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds containing oxygen
    • C08G59/1455Monocarboxylic acids, anhydrides, halides, or low-molecular-weight esters thereof
    • C08G59/1461Unsaturated monoacids
    • C08G59/1466Acrylic or methacrylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/14Polycondensates modified by chemical after-treatment
    • C08G59/1433Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds
    • C08G59/1477Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds containing nitrogen
    • 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
    • C09D5/08Anti-corrosive paints
    • 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
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/20Diluents or solvents
    • 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
    • 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
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2150/00Compositions for coatings
    • C08G2150/90Compositions for anticorrosive coatings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Wood Science & Technology (AREA)
  • Materials Engineering (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Polymers & Plastics (AREA)
  • Medicinal Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Emergency Medicine (AREA)
  • Inorganic Chemistry (AREA)
  • Paints Or Removers (AREA)
  • Macromonomer-Based Addition Polymer (AREA)

Abstract

The invention belongs to the technical field of anticorrosive coatings, and particularly relates to a graphene oxide/epoxy vinyl ester resin heavy-duty solvent-free composite coating as well as a preparation method and application thereof. According to the invention, firstly, half-blocking reaction of diisocyanate is carried out by using an acrylate monomer, then epoxy resin and unsaturated monoacid serving as a diluent are added, grafting reaction is carried out on isocyanate and hydroxyl on the epoxy resin, graphene oxide and dicarboxylic acid are added after the reaction is completed, functional groups on the graphene oxide participate in the reaction, and finally, blocking is carried out on the epoxy resin by using carboxylic acid, so that the graphene oxide/epoxy vinyl ester resin heavy-duty anticorrosive solvent-free composite coating is obtained. The graphene oxide/epoxy vinyl ester resin heavy-duty solvent-free composite coating has excellent barrier property, better corrosion resistance and excellent mechanical property, and no organic solvent is added in the reaction process, so that the harm to the environment is reduced.

Description

Graphene oxide/epoxy vinyl ester resin heavy-duty anti-corrosion solvent-free composite coating and preparation method and application thereof
Technical Field
The invention belongs to the technical field of anticorrosive coatings, and particularly relates to a graphene oxide/epoxy vinyl ester resin heavy-duty solvent-free composite coating as well as a preparation method and application thereof.
Background
As an important component of modern materials, metals and alloys thereof are widely applied in various aspects such as national defense, transportation, mechanical manufacturing, chemical engineering, daily life and the like. However, the metal material is easily corroded or aged by corrosive media such as water, air, chloride ions and the like in the surrounding environment, so that the structure and performance of the metal material are lost. The metal corrosion not only brings loss to national economic development, but also brings hidden troubles to the life health and property safety of people. The most effective and simple method for protecting metals is to apply an organic coating on the surface of the metal to isolate the corrosive medium from the metal substrate.
Graphene is the thinnest anticorrosive material in the world at present, and the research in the anticorrosive field attracts the attention of researchers in various countries in the world. The graphene and the derivatives thereof have excellent barrier property, ultra-large specific surface area, good conductivity, high chemical stability and other properties, and have obvious improvement effects on the comprehensive properties of the anticorrosive coating, such as enhancing the corrosion resistance and wear resistance of the coating, improving the adhesive force of the coating to a base material, and simultaneously having the characteristics of environmental protection, safety, no secondary pollution and the like.
In the prior art, chinese patent application with publication number CN110240851A discloses a graphene epoxy glass flake coating and a preparation method thereof, which comprises a component a and a component B, wherein the component a comprises graphene, epoxy resin, an anti-settling agent, titanium dioxide, glass flakes, a dispersing agent, a filler and a first solvent, and the component B comprises a curing agent, an adhesion promoter and a second solvent.
The Chinese patent application with the publication number of CN109207022A discloses an epoxy glass flake anticorrosive paint and a preparation method and application thereof, and the epoxy glass flake anticorrosive paint comprises a component A and a component B, wherein the component A comprises epoxy resin, glass flakes, pigment, a dispersing agent, a silane coupling agent, a defoaming agent, an auxiliary agent and a solvent, and the component B comprises graphene slurry, nano calcium carbonate, cocoyl diethanol amine and aluminium tripolyphosphate.
However, in the prior art, a large amount of organic solvent and auxiliary agent are added in the preparation process, which is not beneficial to environmental protection, and the product is divided into A, B components, so that incompatibility phenomenon is easy to occur among materials in A, B components, thereby affecting the anticorrosion effect.
Disclosure of Invention
According to a first aspect of the invention, a graphene oxide/epoxy vinyl ester resin heavy-duty solvent-free composite coating is provided, which is prepared from the following raw materials in parts by weight: 30-49 parts of epoxy resin, 3-6 parts of diisocyanate, 9-20 parts of unsaturated monobasic acid, 2-5 parts of acrylate monomer, 2-5 parts of dibasic acid or dibasic anhydride, 0.01-0.3 part of graphene oxide or modified graphene oxide, 30-40 parts of active diluent, 0.1-1 part of first catalyst, 0.1-1 part of second catalyst and 0.01-0.1 part of polymerization inhibitor.
In some embodiments, the modified graphene oxide is obtained by modifying graphene oxide with a silane coupling agent.
In some embodiments, the modified graphene oxide is prepared by the following method: uniformly mixing absolute ethyl alcohol, deionized water and tetraethyl silicate, stirring for 2-4h, then adding graphene oxide, performing ultrasonic treatment for 60-120min, then adding a silane coupling agent, stirring for 2-3h, and performing reflux reaction at 65-75 ℃ for 3-5h to obtain the modified graphene oxide.
In some embodiments, the silane coupling agent is selected from one or more of 3-methacryloxypropyltrimethoxysilane, 3-glycidoxypropyltrimethoxysilane, 3-methacryloxypropyltriethoxysilane, vinyltriethoxysilane, tetraethyl silicate.
In some embodiments, the epoxy resin is selected from one or more of bisphenol A type epoxy resin, bisphenol AD type epoxy resin, bisphenol F type epoxy resin, bisphenol S type epoxy resin with an epoxy equivalent weight of 230-340 g/mol; the diisocyanate is one or more selected from toluene diisocyanate, isophorone diisocyanate, diphenylmethane diisocyanate and hexamethylene diisocyanate.
In some embodiments, the unsaturated monoacid is selected from one or more of acrylic acid, methacrylic acid, crotonic acid; the acrylate monomer is selected from one or more of hydroxyethyl acrylate, hydroxyethyl methacrylate and hydroxypropyl acrylate; the dibasic acid or the dibasic acid anhydride is selected from one or more of fumaric acid, maleic anhydride and phthalic anhydride.
In some embodiments, the first catalyst is selected from dibutyltin dilaurate and the second catalyst is selected from one or more of benzyltriethylammonium chloride, benzyldiamine, triethylamine, diethylamine, triphenylphosphine.
In some embodiments, the polymerization inhibitor is selected from one or more of hydroquinone, p-tert-butylcatechol, catechol; the active diluent is selected from one or more of styrene, alpha-methyl styrene and methyl acrylate.
According to another aspect of the present invention, there is provided a preparation method of the graphene oxide/epoxy vinyl ester resin heavy duty solvent-free composite coating, the preparation method comprises: reacting diisocyanate and an acrylate monomer at 30-50 ℃ for 2-3h, adding epoxy resin, unsaturated monoacid, a polymerization inhibitor, graphene oxide or modified graphene oxide and a first catalyst, heating to 60-80 ℃ for reaction for 2-4h, adding dibasic acid or dibasic acid anhydride and a second catalyst, uniformly stirring, heating to 100-120 ℃ for reaction until the acid value is reduced to below 8mgKOH/g, cooling to 70-90 ℃, adding a reactive diluent, and mixing to obtain the modified graphene oxide.
According to the invention, firstly, half-blocking reaction of diisocyanate is carried out by using an acrylate monomer, then epoxy resin and unsaturated monoacid serving as a diluent are added, grafting reaction is carried out on isocyanate and hydroxyl on the epoxy resin, graphene oxide and dicarboxylic acid are added after the reaction is completed, functional groups on the graphene oxide participate in the reaction, and finally, blocking is carried out on the epoxy resin by using carboxylic acid, so that the graphene oxide/epoxy vinyl ester resin heavy-duty anticorrosive solvent-free composite coating is obtained.
According to still another aspect of the invention, the application of the graphene oxide/epoxy vinyl ester resin heavy-duty solvent-free composite coating in preparing a marine anticorrosive coating is provided. In particular to a heavy anti-corrosion coating for the surface of steel structures or concrete, such as marine engineering facilities such as offshore platforms, ship oil pipelines, large pressure steel pipes of hydropower stations, wharf steel piles, bridges, gates, ballast water tanks, gas pipes, sewage treatment pools, buried pipelines and the like.
Has the advantages that:
the graphene oxide/epoxy vinyl ester resin heavy-duty solvent-free composite coating has excellent barrier property, better corrosion resistance and excellent mechanical property, and no organic solvent is added in the reaction process, so that the harm to the environment is reduced.
According to the invention, the multi-component hyperbranched reaction is carried out on diisocyanate, acrylate monomer, graphene oxide and epoxy resin, so that the crosslinking density of the resin and the dispersibility of the graphene oxide in the resin are increased.
The invention adopts reactant unsaturated monoacid as diluent, thereby avoiding the use of volatile solvent, not only reducing the harm to the environment, but also accelerating the total reaction rate and improving the utilization rate of raw materials.
The anticorrosive coating disclosed by the invention is simple in preparation process and has excellent barrier property, low surface energy and better corrosion resistance.
Drawings
FIG. 1 is a Tafel plot of tinplate coated with different coatings at a coating thickness of 25 μm in the experiment of the present invention.
Detailed Description
The present invention will be described in further detail with reference to specific examples, but the embodiments of the present invention are not limited thereto. The starting materials referred to in the following examples are commercially available.
Example 1
The preparation method of the graphene oxide/epoxy vinyl ester resin heavy-duty solvent-free composite coating comprises the following steps:
6.44g of toluene diisocyanate and hydroquinone serving as a polymerization inhibitor accounting for 0.05 percent of the total mass of the raw materials are put into a three-neck flask with a mechanical stirrer and a constant-pressure separating funnel, nitrogen is introduced, the temperature is raised to 45 ℃, 4.30g of hydroxyethyl acrylate is slowly dripped while stirring, and the reaction is carried out for about 2.5 hours under the protection of nitrogen until the mass percentage of the isocyanate is reduced to half of the initial value. Then, 50.00g of bisphenol A type epoxy resin E-44 (epoxy equivalent 227.27), 13.32g of acrylic acid, 0.06g of dibutyltin dilaurate and 0.02% of graphite oxide were added to a three-necked flask, and the mixture was stirred uniformly, heated to 70 ℃ and reacted for 3.5 hours. Then adding a catalyst benzyltriethylammonium chloride which is 0.6 percent of the total mass of the raw materials and 3.68g of fumaric acid, uniformly stirring, heating to 110 ℃ for reaction until the acid value is reduced to below 8mgKOH/g, cooling to 80 ℃, and finally adding 33.43g of active diluent styrene until the mixture is uniformly mixed to obtain the graphene oxide/epoxy vinyl ester resin heavy-duty anticorrosive solvent-free composite coating.
Example 2
The preparation method of the graphene oxide/epoxy vinyl ester resin heavy-duty solvent-free composite coating comprises the following steps:
6.44g of toluene diisocyanate and hydroquinone serving as a polymerization inhibitor accounting for 0.05 percent of the total mass of the raw materials are put into a three-neck flask with a mechanical stirrer and a constant-pressure separating funnel, nitrogen is introduced, the temperature is raised to 45 ℃, 4.30g of hydroxyethyl acrylate is slowly dripped while stirring, and the reaction is carried out for about 2.5 hours under the protection of nitrogen until the mass percentage of the isocyanate is reduced to half of the initial value. Then 50.00g of bisphenol A epoxy resin E-44 (epoxy equivalent weight 227.27), 13.32g of acrylic acid, 0.06g of dibutyltin dilaurate and graphene oxide accounting for 0.04 percent of the total mass of the raw materials are added into a three-neck flask, the mixture is uniformly stirred, the temperature is raised to 70 ℃, and the reaction is carried out for 3.5 hours. Then adding a catalyst benzyltriethylammonium chloride which is 0.6 percent of the total mass of the raw materials and 3.68g of fumaric acid, uniformly stirring, heating to 110 ℃ for reaction until the acid value is reduced to below 8mgKOH/g, cooling to 80 ℃, and finally adding 33.43g of active diluent styrene until the mixture is uniformly mixed to obtain the graphene oxide/epoxy vinyl ester resin heavy-duty anticorrosive solvent-free composite coating.
Example 3
The preparation method of the modified graphene oxide/epoxy vinyl ester resin heavy-duty solvent-free composite coating of the embodiment comprises the following steps:
(1) 160mL of absolute ethyl alcohol, 30mL of deionized water and 10mL of tetraethyl orthosilicate are uniformly mixed, stirred for 3h at room temperature, then 0.1g of graphene oxide is added, ultrasonic treatment is carried out for 45min, then 2mL of 3-methacryloxypropyl trimethoxysilane and 2mL of 3-glycidoxypropyl trimethoxysilane are added, stirred for 3h at room temperature, then the mixture is transferred into an oil bath kettle for reflux reaction at 70 ℃ for 4h, and discharging, washing with an ethanol water solution and drying are carried out, thus obtaining the modified graphene oxide.
(2) 6.44g of toluene diisocyanate and hydroquinone serving as a polymerization inhibitor with the total mass of 0.028 percent of the raw material are put into a three-neck flask with a mechanical stirrer and a constant-pressure separating funnel, nitrogen is introduced, the temperature is raised to 45 ℃, 4.30g of hydroxyethyl acrylate is slowly dripped while stirring, and the reaction lasts for about 2.5 hours under the protection of nitrogen until the mass percent of the isocyanate is reduced to half of the initial value. Then 50.00g of bisphenol A epoxy resin E-44 (epoxy equivalent weight 227.27), 13.32g of acrylic acid, 0.06g of dibutyltin dilaurate and modified graphene oxide accounting for 0.03 percent of the total mass of the raw materials are added into a three-neck flask, the mixture is uniformly stirred, the temperature is raised to 70 ℃, and the reaction is carried out for 3.5 hours. Then adding a catalyst benzyltriethylammonium chloride accounting for 0.6 percent of the total mass of the raw materials and 3.68g of fumaric acid, uniformly stirring, heating to 110 ℃ for reaction until the acid value is reduced to below 8mgKOH/g, cooling to 80 ℃, and finally adding 33.43g of active diluent styrene until the mixture is uniformly mixed to obtain the modified graphene oxide/epoxy vinyl ester resin heavy-duty anticorrosive solvent-free composite coating.
Example 4
The preparation method of the modified graphene oxide/epoxy vinyl ester resin heavy-duty solvent-free composite coating of the embodiment comprises the following steps:
(1) 160mL of absolute ethyl alcohol, 30mL of deionized water and 10mL of tetraethyl orthosilicate are uniformly mixed, stirred for 3h at room temperature, then 0.1g of graphene oxide is added, ultrasonic treatment is carried out for 45min, then 2mL of 3-methacryloxypropyl trimethoxysilane and 2mL of 3-glycidoxypropyl trimethoxysilane are added, stirred for 3h at room temperature, then the mixture is transferred into an oil bath kettle for reflux reaction at 70 ℃ for 4h, and discharging, washing with an ethanol water solution and drying are carried out, thus obtaining the modified graphene oxide.
(2) 6.44g of toluene diisocyanate and hydroquinone serving as a polymerization inhibitor accounting for 0.05 percent of the total mass of the raw materials are put into a three-neck flask with a mechanical stirrer and a constant-pressure separating funnel, nitrogen is introduced, the temperature is raised to 45 ℃, 4.30g of hydroxyethyl acrylate is slowly dripped while stirring, and the reaction is carried out for about 2.5 hours under the protection of nitrogen until the mass percentage of the isocyanate is reduced to half of the initial value. Then 50.00g of bisphenol A epoxy resin E-44 (epoxy equivalent weight 227.27), 13.32g of acrylic acid, 0.06g of dibutyltin dilaurate and modified graphene oxide accounting for 0.05% of the total mass of the raw materials are added into a three-neck flask, the mixture is uniformly stirred, the temperature is raised to 70 ℃, and the reaction is carried out for 3.5 hours. Then adding a catalyst benzyltriethylammonium chloride accounting for 0.6 percent of the total mass of the raw materials and 3.68g of fumaric acid, uniformly stirring, heating to 110 ℃ for reaction until the acid value is reduced to below 8mgKOH/g, cooling to 80 ℃, and finally adding 33.43g of active diluent styrene until the mixture is uniformly mixed to obtain the modified graphene oxide/epoxy vinyl ester resin heavy-duty anticorrosive solvent-free composite coating.
Example 5
The preparation method of the modified graphene oxide/epoxy vinyl ester resin heavy-duty solvent-free composite coating of the embodiment comprises the following steps:
(1) 160mL of absolute ethyl alcohol, 30mL of deionized water and 10mL of tetraethyl orthosilicate are uniformly mixed, stirred for 3h at room temperature, then 0.1g of graphene oxide is added, ultrasonic treatment is carried out for 45min, then 2mL of 3-methacryloxypropyl trimethoxysilane and 2mL of 3-glycidoxypropyl trimethoxysilane are added, stirred for 3h at room temperature, then the mixture is transferred into an oil bath kettle for reflux reaction at 70 ℃ for 4h, and discharging, washing with an ethanol water solution and drying are carried out, thus obtaining the modified graphene oxide.
(2) 6.44g of toluene diisocyanate and hydroquinone serving as a polymerization inhibitor accounting for 0.05 percent of the total mass of the raw materials are put into a three-neck flask with a mechanical stirrer and a constant-pressure separating funnel, nitrogen is introduced, the temperature is raised to 45 ℃, 4.30g of hydroxyethyl acrylate is slowly dripped while stirring, and the reaction is carried out for about 2.5 hours under the protection of nitrogen until the mass percentage of the isocyanate is reduced to half of the initial value. Then 50.00g of bisphenol A epoxy resin E-44 (epoxy equivalent weight 227.27), 14.50g of acrylic acid, 0.06g of dibutyltin dilaurate and modified graphene oxide accounting for 0.03 percent of the total mass of the raw materials are added into a three-neck flask, the mixture is uniformly stirred, the temperature is raised to 70 ℃, and the reaction is carried out for 3.5 hours. Then adding a catalyst benzyltriethylammonium chloride accounting for 0.6 percent of the total mass of the raw materials and 2.26g of maleic anhydride, uniformly stirring, heating to 110 ℃ for reaction until the acid value is reduced to below 8mgKOH/g, cooling to 80 ℃, and finally adding 33.43g of active diluent styrene until the mixture is uniformly mixed to obtain the modified graphene oxide/epoxy vinyl ester resin heavy-duty anticorrosive solvent-free composite coating.
Comparative example 1
Epoxy glass flake coatings (IPN8710, produced by Jiasheng coatings of Cangzhou, using epoxy resin as the main base material and glass flakes as the filler).
Next, the graphene oxide/epoxy vinyl ester resin heavy duty solvent-free composite coating prepared in examples 1 to 2, the modified graphene oxide/epoxy vinyl ester resin heavy duty solvent-free composite coating prepared in examples 3 to 5, and the epoxy glass flake coating of comparative example 1 were coated on polished tinplate, and the corrosion resistance and mechanical properties were tested by the following test methods:
1. chemical corrosion resistance test: and respectively soaking the cured film coated on the polished tinplate in a 10% NaOH solution, a 10% HCl solution and a 3.5% NaCl solution for 15 days, taking out the cured film, and observing whether the cured film has the phenomena of bubbling, rusting, falling off and the like.
2. Salt spray resistance test: and (3) performing a salt spray resistance test on the curing film coated on the polished tinplate by using a BGD 880/S salt spray corrosion test box.
3. Tensile strength and fracture growth rate: and (3) testing the mechanical property of the casting body of the cured film coated on the polished tinplate according to the national standard GB/T1040.3-2006.
The test results are shown in table 1.
TABLE 1 paint Performance test results
Detecting items Example 1 Example 2 Example 3 Example 4 Example 5 Comparative example
Tolerance of 10%NaOHSolution/15 d Is free of Is free of Is free of Is free of Is free of Foaming
Tolerance of 10%HClSolution/15 d Is free of Is free of Is free of Is free of Is free of Foaming
3.5 percent of the total weightNaClSolution/15 d Is free of Is free of Is free of Is free of Is free of Is free of
Salt spray resistance per 1000h Is free of Is free of Is free of Is free of Is free of Rust formation
Tensile strength-MPa 79.44 81.29 88.73 87.76 85.25 70.11
Percentage of growth at break/%) 14.49 13.27 16.63 14.45 15.54 9.6
Note: "none" in Table 1 means no blistering, rusting, flaking, etc.
As can be seen from table 1, compared with the epoxy glass flake coating of comparative example 1, the graphene oxide/epoxy vinyl ester resin heavy duty solvent-free composite coating and the modified graphene oxide/epoxy vinyl ester resin heavy duty solvent-free composite coating of the present invention have better corrosion resistance to corrosive media such as acid, alkali, water, air, and chloride ions, and better mechanical properties.
Then, in order to further detect the corrosion resistance of the composite coating of the present invention, the graphene oxide/epoxy vinyl ester resin heavy duty solvent-free composite coating prepared in example 1, the modified graphene oxide/epoxy vinyl ester resin heavy duty solvent-free composite coatings prepared in examples 3 to 4, and the epoxy glass flake coating of comparative example 1 were coated on polished tinplate to a coating thickness of 25 μm, and the corrosion rate of tinplate was determined by tafel curve.
The test method specifically comprises the following steps: the corrosion resistance of the metal coating is characterized by a testing method of a potentiodynamic polarization curve by using a CHI660E electrochemical workstation, a three-electrode electrolytic cell system is used in the test, a tinplate is used as a working electrode, a platinum electrode is used as a counter electrode, an Ag/AgCl system is used as a reference electrode, and a 3.5 wt% sodium chloride aqueous solution is used as an electrolyte medium. The coating was applied to the working electrode in a 1cm x 1cm format and tested at open circuit potential.
The results of the detection are shown in FIG. 1. As can be seen from fig. 1, the corrosion current (Icorr) of the tinplate coated with the composite coating of the present invention is significantly lower and the corrosion potential (Ecorr) is significantly increased than that of the tinplate coated with the coating of comparative example 1, thereby indicating that the composite coating of the present invention has better corrosion resistance.
The above embodiments are preferred embodiments of the present invention, but the present invention is not limited to the above embodiments, and any other changes, modifications, substitutions, combinations, and simplifications which do not depart from the spirit and principle of the present invention should be construed as equivalents thereof, and all such changes, modifications, substitutions, combinations, and simplifications are intended to be included in the scope of the present invention.

Claims (10)

1. The graphene oxide/epoxy vinyl ester resin heavy-duty anticorrosive solvent-free composite coating is characterized by being prepared from the following raw materials in parts by weight: 30-49 parts of epoxy resin, 3-6 parts of diisocyanate, 9-20 parts of unsaturated monobasic acid, 2-5 parts of acrylate monomer, 2-5 parts of dibasic acid or dibasic anhydride, 0.01-0.3 part of graphene oxide or modified graphene oxide, 30-40 parts of active diluent, 0.1-1 part of first catalyst, 0.1-1 part of second catalyst and 0.01-0.1 part of polymerization inhibitor.
2. The graphene oxide/epoxy vinyl ester resin heavy-duty solvent-free composite coating according to claim 1, wherein the modified graphene oxide is obtained by modifying graphene oxide with a silane coupling agent.
3. The graphene oxide/epoxy vinyl ester resin heavy duty solvent-free composite coating according to claim 2, wherein the modified graphene oxide is prepared by the following method: mixing absolute ethyl alcohol, deionized water and tetraethyl silicate, stirring for 2-4h, then adding graphene oxide, performing ultrasonic treatment for 60-120min, then adding a silane coupling agent, stirring for 2-3h, and performing reflux reaction at 65-75 ℃ for 3-5h to obtain the modified graphene oxide.
4. The graphene oxide/epoxy vinyl ester resin heavy duty solvent-free composite coating according to claim 2 or 3, wherein the silane coupling agent is selected from one or more of 3-methacryloxypropyltrimethoxysilane, 3-glycidoxypropyltrimethoxysilane, 3-methacryloxypropyltriethoxysilane, vinyltriethoxysilane, and tetraethyl silicate.
5. The graphene oxide/epoxy vinyl ester resin heavy-duty solvent-free composite coating as claimed in claim 1, wherein the epoxy resin is selected from one or more of bisphenol A type epoxy resin, bisphenol AD type epoxy resin, bisphenol F type epoxy resin and bisphenol S type epoxy resin with an epoxy equivalent of 230-340 g/mol; the diisocyanate is selected from one or more of toluene diisocyanate, isophorone diisocyanate, diphenylmethane diisocyanate and hexamethylene diisocyanate.
6. The graphene oxide/epoxy vinyl ester resin heavy duty solvent-free composite coating according to claim 1, wherein the unsaturated monobasic acid is selected from one or more of acrylic acid, methacrylic acid and crotonic acid; the acrylate monomer is selected from one or more of hydroxyethyl acrylate, hydroxyethyl methacrylate and hydroxypropyl acrylate; the dibasic acid or the dibasic acid anhydride is selected from one or more of fumaric acid, maleic anhydride and phthalic anhydride.
7. The graphene oxide/epoxy vinyl ester resin heavy duty solvent-free composite coating according to claim 1, wherein the first catalyst is selected from dibutyltin dilaurate, and the second catalyst is selected from one or more of benzyltriethylammonium chloride, benzyldiamine, triethylamine, diethylamine, and triphenylphosphine.
8. The graphene oxide/epoxy vinyl ester resin heavy-duty solvent-free composite coating according to claim 1, wherein the polymerization inhibitor is one or more selected from hydroquinone, p-tert-butylcatechol, and catechol; the reactive diluent is selected from one or more of styrene, alpha-methyl styrene and methyl acrylate.
9. The preparation method of the graphene oxide/epoxy vinyl ester resin heavy-duty solvent-free composite coating according to any one of claims 1 to 8, characterized in that the preparation method comprises the following steps: reacting diisocyanate and an acrylate monomer at 30-50 ℃ for 2-3h, adding epoxy resin, unsaturated monoacid, a polymerization inhibitor, graphene oxide or modified graphene oxide and a first catalyst, heating to 60-80 ℃ for reaction for 2-4h, adding dibasic acid or dibasic acid anhydride and a second catalyst, uniformly stirring, heating to 100-120 ℃ for reaction until the acid value is reduced to below 8mgKOH/g, cooling to 70-90 ℃, adding a reactive diluent, and mixing to obtain the modified graphene oxide.
10. Use of the graphene oxide/epoxy vinyl ester resin heavy duty solvent-free composite coating according to any one of claims 1 to 8 in the preparation of marine anticorrosive coatings.
CN202110878510.9A 2021-07-30 2021-07-30 Graphene oxide/epoxy vinyl ester resin heavy-duty anti-corrosion solvent-free composite coating and preparation method and application thereof Active CN113512341B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202110878510.9A CN113512341B (en) 2021-07-30 2021-07-30 Graphene oxide/epoxy vinyl ester resin heavy-duty anti-corrosion solvent-free composite coating and preparation method and application thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202110878510.9A CN113512341B (en) 2021-07-30 2021-07-30 Graphene oxide/epoxy vinyl ester resin heavy-duty anti-corrosion solvent-free composite coating and preparation method and application thereof

Publications (2)

Publication Number Publication Date
CN113512341A true CN113512341A (en) 2021-10-19
CN113512341B CN113512341B (en) 2022-08-12

Family

ID=78068924

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202110878510.9A Active CN113512341B (en) 2021-07-30 2021-07-30 Graphene oxide/epoxy vinyl ester resin heavy-duty anti-corrosion solvent-free composite coating and preparation method and application thereof

Country Status (1)

Country Link
CN (1) CN113512341B (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114539551A (en) * 2022-03-23 2022-05-27 华南农业大学 Modified graphene oxide/elaeostearic acid maleic anhydride vinyl ester anticorrosive resin and preparation method and application thereof
CN115286767A (en) * 2022-06-30 2022-11-04 海洋化工研究院有限公司 Antibacterial fluorine modified epoxy vinyl ester resin, preparation method thereof and multi-mechanism synergetic universal anticorrosive coating
CN115895325A (en) * 2022-09-27 2023-04-04 浩力森化学科技(江苏)有限公司 Graphene auxiliary agent, main resin, electrophoretic coating emulsion and preparation method thereof
CN116355123A (en) * 2023-04-06 2023-06-30 安庆瑞泰化工有限公司 Acrylic coating resin for optical film and preparation method thereof
CN116574427A (en) * 2023-03-09 2023-08-11 浙江飞鲸新材料科技股份有限公司 Marine steel structure long-acting protective multilayer epoxy heavy-duty anticorrosive coating and preparation method thereof

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0360188A2 (en) * 1988-09-23 1990-03-28 Vianova Kunstharz Aktiengesellschaft Process for the production of low-viscosity binders drying in the air for quickly drying paints rich in solids
CN108341921A (en) * 2018-03-27 2018-07-31 佛山市三求光固材料股份有限公司 Polyurethane-modified flexible epoxy acrylic resin, preparation method, photocuring marking ink and flexible circuit board
US20190194417A1 (en) * 2017-12-21 2019-06-27 Palo Alto Research Center Incorporated Functionalized graphene oxide curable formulations
CN110003751A (en) * 2019-03-22 2019-07-12 华南理工大学 A kind of modified graphene oxide/acrylic resin composite anticorrosion coating and its preparation and application
US20200019033A1 (en) * 2018-07-16 2020-01-16 Polyceed Inc. Insulated Glass Unit Utilizing Electrochromic Elements
CN111073433A (en) * 2020-01-02 2020-04-28 孙夏芬 Exterior wall heat-insulating coating and preparation method thereof
CN113150245A (en) * 2021-04-30 2021-07-23 华南农业大学 Modified vinyl ester resin and preparation method thereof, toughened and modified vinyl ester resin with good air-drying property and preparation method and application thereof

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0360188A2 (en) * 1988-09-23 1990-03-28 Vianova Kunstharz Aktiengesellschaft Process for the production of low-viscosity binders drying in the air for quickly drying paints rich in solids
US20190194417A1 (en) * 2017-12-21 2019-06-27 Palo Alto Research Center Incorporated Functionalized graphene oxide curable formulations
CN108341921A (en) * 2018-03-27 2018-07-31 佛山市三求光固材料股份有限公司 Polyurethane-modified flexible epoxy acrylic resin, preparation method, photocuring marking ink and flexible circuit board
US20200019033A1 (en) * 2018-07-16 2020-01-16 Polyceed Inc. Insulated Glass Unit Utilizing Electrochromic Elements
CN110003751A (en) * 2019-03-22 2019-07-12 华南理工大学 A kind of modified graphene oxide/acrylic resin composite anticorrosion coating and its preparation and application
CN111073433A (en) * 2020-01-02 2020-04-28 孙夏芬 Exterior wall heat-insulating coating and preparation method thereof
CN113150245A (en) * 2021-04-30 2021-07-23 华南农业大学 Modified vinyl ester resin and preparation method thereof, toughened and modified vinyl ester resin with good air-drying property and preparation method and application thereof

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114539551A (en) * 2022-03-23 2022-05-27 华南农业大学 Modified graphene oxide/elaeostearic acid maleic anhydride vinyl ester anticorrosive resin and preparation method and application thereof
CN114539551B (en) * 2022-03-23 2023-08-25 华南农业大学 Modified graphene oxide/tung oil acid maleic anhydride vinyl ester anti-corrosion resin and preparation method and application thereof
CN115286767A (en) * 2022-06-30 2022-11-04 海洋化工研究院有限公司 Antibacterial fluorine modified epoxy vinyl ester resin, preparation method thereof and multi-mechanism synergetic universal anticorrosive coating
CN115286767B (en) * 2022-06-30 2023-09-19 海洋化工研究院有限公司 Antibacterial fluorine modified epoxy vinyl ester resin, preparation method thereof and multi-mechanism synergistic general anti-corrosion coating
CN115895325A (en) * 2022-09-27 2023-04-04 浩力森化学科技(江苏)有限公司 Graphene auxiliary agent, main resin, electrophoretic coating emulsion and preparation method thereof
CN115895325B (en) * 2022-09-27 2023-11-14 浩力森化学科技(江苏)有限公司 Graphene auxiliary agent, main resin, electrophoretic coating emulsion and preparation method thereof
CN116574427A (en) * 2023-03-09 2023-08-11 浙江飞鲸新材料科技股份有限公司 Marine steel structure long-acting protective multilayer epoxy heavy-duty anticorrosive coating and preparation method thereof
CN116574427B (en) * 2023-03-09 2024-03-19 浙江飞鲸新材料科技股份有限公司 Marine steel structure long-acting protective multilayer epoxy heavy-duty anticorrosive coating and preparation method thereof
CN116355123A (en) * 2023-04-06 2023-06-30 安庆瑞泰化工有限公司 Acrylic coating resin for optical film and preparation method thereof

Also Published As

Publication number Publication date
CN113512341B (en) 2022-08-12

Similar Documents

Publication Publication Date Title
CN113512341B (en) Graphene oxide/epoxy vinyl ester resin heavy-duty anti-corrosion solvent-free composite coating and preparation method and application thereof
US8420219B2 (en) Method for the application of corrosion-resistant layers to metallic surfaces
CN109370364B (en) Nano anticorrosive paint for metal surface in acid-related environment and preparation method thereof
JP3259274B2 (en) Cationic electrodeposition coating method and cationic electrodeposition coating composition
JPH0689274B2 (en) Cationic electrodeposition composition improved using sulfamic acid and its derivatives
JP2009221464A (en) Water-based coating composition, and coating method using the composition
CN113698842A (en) Solvent-free heavy-duty anticorrosive paint and preparation process thereof
CN107429108B (en) Anticorrosive coating film, method for forming same, and anticorrosive coating composition for forming anticorrosive coating film
CN109880484A (en) A kind of water-base epoxy thickness slurry anti-decaying paint and its preparation method and application
CN109181480B (en) Epoxy zinc-rich coating containing modified titanium dioxide, preparation method and application
CN111334161A (en) Flexible self-repairing anticorrosive coating for inner wall of seawater steel pipeline and preparation method thereof
JP5005964B2 (en) Anionic electrodeposition coating composition
CN110845879A (en) Novel environment-friendly water-based paint and preparation method thereof
CN115286767B (en) Antibacterial fluorine modified epoxy vinyl ester resin, preparation method thereof and multi-mechanism synergistic general anti-corrosion coating
WO1998003595A1 (en) Electrodeposition coating composition having electrodeposition potentiality and process for electrodeposition coating
CN115058171A (en) Low-surface-treatment water-based paint for station house steel structure and preparation method thereof
CN108641543B (en) Marine anticorrosive paint based on liquid metal and preparation method thereof
JP2013064069A (en) Rust-prevention coating composition
US6262146B1 (en) Aliphatic hydrocarbon group-containing resin composition for cationic electrocoating and cationic electrocoating composition
KR20220062322A (en) Aqueous Dispersion of Polymer Particles
CN116199890A (en) Styrene-maleic anhydride copolymer functionalized graphene oxide modified vinyl ester resin and preparation method and application thereof
CN115820091A (en) Preparation of GO-PDA-CeO 2 Method for preparing PU wear-resistant super-hydrophobic long-acting anti-corrosion coating
US4933380A (en) Air-drying aqueous coating composition for electrodeposition
CN113861781A (en) Super quick-drying and rapidly-packaged thick-coating type single-component water-based anticorrosive coating for cast pipe
JPS59123574A (en) Corrosion preventive coating method

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant