CN114410140A - Coating and preparation method thereof - Google Patents

Coating and preparation method thereof Download PDF

Info

Publication number
CN114410140A
CN114410140A CN202210129002.5A CN202210129002A CN114410140A CN 114410140 A CN114410140 A CN 114410140A CN 202210129002 A CN202210129002 A CN 202210129002A CN 114410140 A CN114410140 A CN 114410140A
Authority
CN
China
Prior art keywords
parts
stirring
mixture
dispersing
coating
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.)
Pending
Application number
CN202210129002.5A
Other languages
Chinese (zh)
Inventor
岑卫康
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to CN202210129002.5A priority Critical patent/CN114410140A/en
Publication of CN114410140A publication Critical patent/CN114410140A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D4/00Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
    • C09D4/06Organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond in combination with a macromolecular compound other than an unsaturated polymer of groups C09D159/00 - C09D187/00
    • 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
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/18Fireproof paints including high temperature resistant 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
    • C09D7/40Additives
    • C09D7/60Additives non-macromolecular
    • C09D7/61Additives non-macromolecular inorganic
    • 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
    • C09D7/63Additives non-macromolecular organic
    • 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
    • C09D7/65Additives macromolecular
    • 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
    • C09D7/70Additives characterised by shape, e.g. fibres, flakes or microspheres

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Paints Or Removers (AREA)

Abstract

A coating and a preparation method thereof comprise a raw material component mixture A, 40-45 parts of titanium dioxide sol, 15-20 parts of isocyanate, 30-40 parts of polyethylene glycol, 10-15 parts of cosolvent, 5-8 parts of talcum powder, 7-12 parts of silicon dioxide dispersion liquid, 5-15 parts of aluminum silicate fiber, 1.5-2 parts of isobutyl acrylate, 5-10 parts of allyl phosphate, 20-30 parts of copper pyrithione, 10-20 parts of film forming agent, 1.6-2 parts of dispersant and 1-5 parts of polyethyleneimine, and the coating is prepared under the coordination of preparation process steps and technical parameters and at least has the following advantages: the paint has the advantages of high glossiness, high temperature resistance, good surface hardness, high corrosion resistance, good adhesiveness, difficult shedding, strong contact adhesive force with the metal surface, high paint film hardness, good coloring effect, difficult agglomeration, suitability for surface treatment decoration of various metals, good comprehensive performance even in a high-temperature environment and obvious improvement on the performance of the paint.

Description

Coating and preparation method thereof
Technical Field
The invention belongs to the field of coatings, and particularly relates to a coating and a preparation method thereof.
Background
In industrial production and daily life, a coating is often used, which is a continuous film coated on the surface of a protected or decorated object and can be firmly attached to the object to be coated, so as to protect and increase the use performance of the product. The protection of metal materials which are easy to corrode or rust needs to be protected by coating, and particularly, the iron products need to be sprayed for improving the service performance and preventing rust, so that the iron products have high gloss, high temperature resistance, good surface hardness and high corrosion resistance. However, although the coating in the current market has the corrosion resistance and can protect the metal surface, the actual application effect is not ideal, the gloss is poor, the adhesion is poor, the coating is easy to fall off under the high-temperature condition, the surface hardness and the corrosion resistance are insufficient, the paint film hardness of the coating is not high, the coating does not have a good coloring effect, and the coating is easy to agglomerate and cannot achieve the effect expected by people.
Disclosure of Invention
The paint is prepared by matching specific raw materials of a mixture A, a mixture B, a mixture C and a mixture D with components, reasonable preparation steps and technical parameters, has high glossiness, high temperature resistance, good surface hardness and high corrosion resistance, is suitable for surface treatment decoration of various metals, has good comprehensive performance even in a high-temperature environment, has good adhesion, is not easy to fall off, has strong contact adhesive force with the metal surface, has high paint film hardness, is not easy to damage, also has a good coloring effect, is not easy to agglomerate, and obviously improves the performance of the paint.
The invention is realized by the following technical scheme: the coating comprises the following raw materials in parts by weight: the coating comprises, by weight, 10-20 parts of a mixture A, 40-45 parts of titanium dioxide sol, 15-20 parts of isocyanate, 30-40 parts of polyethylene glycol, 10-15 parts of a cosolvent, 5-8 parts of talcum powder, 7-12 parts of silica dispersion, 5-15 parts of aluminum silicate fiber, 1.5-2 parts of isobutyl acrylate, 5-10 parts of allyl phosphate, 20-30 parts of copper pyrithione, 10-20 parts of a film forming agent, 1.6-2 parts of a dispersing agent and 1-5 parts of polyethyleneimine.
The mixture A is 1.5-2 parts of polyoxypropylene glycerol ether, 10-15 parts of silica sol, 10-20 parts of deionized water and 10-20 parts of isobutyl acrylate, and is prepared by stirring and dispersing for 20-25 min at normal temperature.
The mixture A is 1.5-2 parts of polyoxypropylene glycerol ether, 10-15 parts of silica sol, 10-20 parts of deionized water, 10-20 parts of isobutyl acrylate and 5-10 parts of conductive mica powder, static electricity is introduced into an insulating plastic barrel, and stirring and dispersing are carried out for 20-25 min, so that the conductive mica powder is prepared.
The titanium dioxide sol is nano titanium dioxide sol.
The cosolvent is any one of sodium salicylate and p-aminobenzoic acid.
A preparation method of the coating comprises the following steps: (1) step 1: adding 1.5-2 parts of polyoxypropylene glycerol ether, 10-15 parts of silica sol, 10-20 parts of deionized water and 10-20 parts of isobutyl acrylate into a first reaction container, and stirring and dispersing for 20-25 min at normal temperature to obtain a mixture A for later use.
(2) Step 2: and (2) adding 40-45 parts of titanium dioxide sol, 15-20 parts of isocyanate and 30-40 parts of polyethylene glycol into a second reaction container, heating to 50 ℃, stirring for 30min, adding the mixture A obtained in the step (1), and stirring and dispersing for 30-40 min to obtain a mixture B.
(3) And step 3: and (3) adding 10-15 parts of cosolvent and 5-8 parts of talcum powder into the mixture B obtained in the step (2), and stirring and dispersing for 20-30 min until the whole system is uniformly mixed to obtain a mixture C.
(4) And 4, step 4: adding 7-12 parts of silicon dioxide dispersion liquid and 1.5-2 parts of isobutyl acrylate into a third reaction container, heating to 50-60 ℃, stirring for 15min, adding 5-10 parts of allyl phosphate and 5-15 parts of aluminum silicate fiber into the reaction container, keeping the temperature at 50-60 ℃, stirring for 30min, adding the mixture C obtained in the step (3), stirring and dispersing for 30-40 min, and mixing the whole system uniformly to obtain a mixture D.
(5) And 5: and (4) adding 20-30 parts of copper pyrithione, 10-20 parts of film forming agent, 1.6-2 parts of dispersing agent and 1-5 parts of polyethyleneimine into the mixture D obtained in the step (4), and stirring and dispersing for 10-15 min under the stirring condition of 600-800 rpm to obtain the coating.
The invention has the beneficial effects that: a coating is prepared from a specific raw material component mixture A, titanium dioxide sol, isocyanate, polyethylene glycol, a cosolvent, talcum powder, silicon dioxide dispersion liquid, aluminum silicate fiber, isobutyl acrylate, allyl phosphate, copper pyrithione, a film-forming agent, a dispersing agent, polyethyleneimine and polyoxypropylene glycerol ether by matching preparation process steps and technical parameters, and has at least the following advantages: the paint has the advantages of high glossiness, high temperature resistance, good surface hardness, high corrosion resistance, good adhesiveness, difficult shedding, strong contact adhesive force with the metal surface, high paint film hardness, good coloring effect, difficult agglomeration, suitability for surface treatment decoration of various metals, good comprehensive performance even in a high-temperature environment and obvious improvement on the performance of the paint.
Detailed Description
The present invention will be described in detail below with reference to examples.
The examples, in which specific conditions are not specified, were conducted under conventional conditions or conditions recommended by the manufacturer. The reagents or instruments used are not indicated by the manufacturer, and are all conventional products commercially available.
In the following embodiments 1 to 3, the prepared coating is coated on the surface of a metal material which is easy to corrode or other materials which need a protective layer, so that a coating is formed, and the coating has the advantages of good adhesiveness, difficult shedding, strong contact adhesive force with the metal surface, high paint film hardness and good comprehensive performance. In the embodiment 4, the prepared coating is sprayed on the surface of a metal material which is easy to corrode by using an electrostatic spraying gun to form a coating which has good adhesiveness, is not easy to fall off, has strong contact adhesive force with the metal surface, has high film hardness and has good comprehensive performance.
Example 1: the coating comprises the following raw materials in parts by weight: the coating comprises, by weight, 10-20 parts of a mixture A, 40-45 parts of titanium dioxide sol, 15-20 parts of isocyanate, 30-40 parts of polyethylene glycol, 5-8 parts of talcum powder, 7-12 parts of silicon dioxide dispersion liquid, 5-15 parts of aluminum silicate fiber, 1.5-2 parts of isobutyl acrylate, 5-10 parts of allyl phosphate, 20-30 parts of copper pyrithione, 10-20 parts of a film forming agent, 1.6-2 parts of a dispersing agent, 1-5 parts of polyethyleneimine and 1.5-2 parts of polyoxypropylene glycerol ether.
The mixture A is 1.5-2 parts of polyoxypropylene glycerol ether, 10-15 parts of silica sol, 10-20 parts of deionized water and 10-20 parts of isobutyl acrylate, and is prepared by stirring and dispersing for 20-25 min at normal temperature.
The titanium dioxide sol is nano titanium dioxide sol.
The cosolvent is any one of sodium salicylate and p-aminobenzoic acid.
The preparation method comprises the following steps: (1) step 1: adding 1.5-2 parts of polyoxypropylene glycerol ether, 10-15 parts of silica sol, 10-20 parts of deionized water and 10-20 parts of isobutyl acrylate into a first reaction container, and stirring and dispersing for 20-25 min at normal temperature to obtain a mixture A for later use.
(2) Step 2: and (2) adding 40-45 parts of titanium dioxide sol, 15-20 parts of isocyanate and 30-40 parts of polyethylene glycol into a second reaction container, heating to 50 ℃, stirring for 30min, adding the mixture A obtained in the step (1), and stirring and dispersing for 30-40 min to obtain a mixture B.
(3) And step 3: and (3) adding 10-15 parts of cosolvent and 5-8 parts of talcum powder into the step (2), stirring and dispersing for 20-30 min until the whole system is uniformly mixed, and thus obtaining a mixture C.
(4) And 4, step 4: adding 7-12 parts of silicon dioxide dispersion liquid and 1.5-2 parts of isobutyl acrylate into a third reaction container, heating to 50-60 ℃, stirring for 15min, adding 5-10 parts of allyl phosphate and 5-15 parts of aluminum silicate fiber into the reaction container, keeping the temperature at 50-60 ℃, stirring for 30min, adding the mixture C obtained in the step (3), stirring and dispersing for 30-40 min, and mixing the whole system uniformly to obtain a mixture D.
(5) And 5: and (4) adding 20-30 parts of copper pyrithione, 10-20 parts of film forming agent, 1.6-2 parts of dispersing agent and 1-5 parts of polyethyleneimine into the mixture D obtained in the step (4), and stirring and dispersing for 10-15 min under the stirring condition of 600-800 rpm to obtain the coating.
Example 2: the coating comprises the following raw materials in parts by weight: the coating comprises, by weight, 13-17 parts of a mixture A, 41-44 parts of titanium dioxide sol, 16-18 parts of isocyanate, 33-37 parts of polyethylene glycol, 12-14 parts of a cosolvent, 6-8 parts of talcum powder, 8-10 parts of silica dispersion, 8-13 parts of aluminum silicate fiber, 1.6-1.8 parts of isobutyl acrylate, 6-8 parts of allyl phosphate, 23-27 parts of copper pyrithione, 13-16 parts of a film forming agent, 1.7-1.9 parts of a dispersing agent, 2-4 parts of polyethyleneimine and 1.6-1.8 parts of polyoxypropylene glycerol ether.
The mixture A is 1.6-1.8 parts of polyoxypropylene glycerol ether, 11-13 parts of silica sol, 14-17 parts of deionized water and 13-17 parts of isobutyl acrylate, and is prepared by stirring and dispersing for 20-25 min at normal temperature.
The preparation method comprises the following steps: (1) step 1: adding 1.6-1.8 parts of polyoxypropylene glycerol ether, 11-13 parts of silica sol, 14-17 parts of deionized water and 13-17 parts of isobutyl acrylate into a first reaction container, stirring and dispersing for 20-25 min at normal temperature to obtain a mixture A for later use.
(2) Step 2: and (2) adding 41-44 parts of titanium dioxide sol, 16-18 parts of isocyanate and 33-37 parts of polyethylene glycol into a second reaction container, heating to 50 ℃, stirring for 30min, adding the mixture A obtained in the step (1), and stirring and dispersing for 30-40 min to obtain a mixture B.
(3) And step 3: and (3) adding 12-14 parts of cosolvent and 6-8 parts of talcum powder into the step (2), and stirring and dispersing for 20-30 min until the whole system is uniformly mixed to obtain a mixture C.
(4) And 4, step 4: adding 8-10 parts of silicon dioxide dispersion liquid and 1.6-1.8 parts of isobutyl acrylate into a third reaction container, heating to 50-60 ℃, stirring for 15min, adding 6-8 parts of allyl phosphate and 8-13 parts of aluminum silicate fiber into the third reaction container, keeping the temperature at 50-60 ℃, stirring for 30min, adding the mixture C obtained in the step (3), stirring and dispersing for 30-40 min, and uniformly mixing the whole system to obtain a mixture D.
(5) And 5: and (4) adding 23-27 parts of copper pyrithione, 13-16 parts of film forming agent, 1.7-1.9 parts of dispersing agent and 2-4 parts of polyethyleneimine into the mixture D obtained in the step (4), and stirring and dispersing for 10-15 min under the stirring condition of 600-800 rpm to obtain the coating.
Example 3: the coating comprises the following raw materials in parts by weight: the coating comprises, by weight, 14-15 parts of a mixture A, 42-43 parts of titanium dioxide sol, 16-17 parts of isocyanate, 34-35 parts of polyethylene glycol, 12-13 parts of a cosolvent, 6-7 parts of talcum powder, 8-9 parts of silica dispersion, 10-11 parts of aluminum silicate fiber, 1.6-1.7 parts of isobutyl acrylate, 6-7 parts of allyl phosphate, 25-26 parts of copper pyrithione, 14-15 parts of a film forming agent, 1.7-1.8 parts of a dispersing agent, 3-4 parts of polyethyleneimine and 1.7-1.8 parts of polyoxypropylene glycerol ether.
The mixture A is 1.6-1.7 parts of polyoxypropylene glycerol ether, 11-12 parts of silica sol, 15-16 parts of deionized water and 14-15 parts of isobutyl acrylate, and is prepared by stirring and dispersing for 20-25 min at normal temperature.
The preparation method comprises the following steps: (1) step 1: adding 1.6-1.7 parts of polyoxypropylene glycerol ether, 11-12 parts of silica sol, 15-16 parts of deionized water and 14-15 parts of isobutyl acrylate into a first reaction container, stirring and dispersing for 20-25 min at normal temperature to obtain a mixture A for later use.
(2) Step 2: and (3) adding 42-43 parts of titanium dioxide sol, 16-17 parts of isocyanate and 34-35 parts of polyethylene glycol into a second reaction container, heating to 50 ℃, stirring for 30min, adding the mixture A obtained in the step (1), and stirring and dispersing for 30-40 min to obtain a mixture B.
(3) And step 3: and (3) adding 12-13 parts of cosolvent and 6-7 parts of talcum powder into the step (2), and stirring and dispersing for 20-30 min until the whole system is uniformly mixed to obtain a mixture C.
(4) And 4, step 4: adding 8-9 parts of silicon dioxide dispersion liquid and 1.6-1.7 parts of isobutyl acrylate into a third reaction container, heating to 50-60 ℃, stirring for 15min, adding 6-7 parts of allyl phosphate and 10-11 parts of aluminum silicate fiber into the reaction container, keeping the temperature at 50-60 ℃, stirring for 30min, adding the mixture C obtained in the step (3), stirring and dispersing for 30-40 min, and uniformly mixing the whole system to obtain a mixture D. (5) And 5: and (4) adding 24-25 parts of copper pyrithione, 14-15 parts of film forming agent, 1.7-1.8 parts of dispersing agent and 3-4 parts of polyethyleneimine into the mixture D obtained in the step (4), and stirring and dispersing for 10-15 min under the stirring condition of 600-800 rpm to obtain the coating.
Example 4 is one coating that can be used for electrostatic spraying: the feed comprises the following raw materials in parts by weight: the coating comprises, by weight, 10-20 parts of a mixture A, 40-45 parts of titanium dioxide sol, 15-20 parts of isocyanate, 30-40 parts of polyethylene glycol, 10-15 parts of a cosolvent, 5-8 parts of talcum powder, 7-12 parts of silica dispersion, 5-15 parts of aluminum silicate fiber, 1.5-2 parts of isobutyl acrylate, 5-10 parts of allyl phosphate, 20-30 parts of copper pyrithione, 10-20 parts of a film forming agent, 1.6-2 parts of a dispersing agent and 1-5 parts of polyethyleneimine.
The mixture A is 1.5-2 parts of polyoxypropylene glycerol ether, 10-15 parts of silica sol, 10-20 parts of deionized water, 10-20 parts of isobutyl acrylate and 5-10 parts of conductive mica powder, static electricity is introduced into an insulating plastic barrel, and stirring and dispersing are carried out for 20-25 min, so that the conductive mica powder is prepared.
Without limitation, the static electricity in the mixture A is 5000-15000 volts, preferably 10000 volts.
A preparation method of the coating comprises the following steps: (1) step 1: adding 1.5-2 parts of polyoxypropylene glycerol ether, 10-15 parts of silica sol, 10-20 parts of deionized water, 10-20 parts of isobutyl acrylate and 5-10 parts of conductive mica powder into a reaction container of an insulating plastic barrel, introducing 10000V static electricity into the insulating plastic barrel, stirring and dispersing for 20-25 min to obtain a mixture A for later use.
(2) Step 2: and (2) adding 40-45 parts of titanium dioxide sol, 15-20 parts of isocyanate and 30-40 parts of polyethylene glycol into a second reaction container, heating to 50 ℃, stirring for 30min, adding the mixture A obtained in the step (1), and stirring and dispersing for 30-40 min to obtain a mixture B.
(3) And step 3: and (3) adding 10-15 parts of cosolvent and 5-8 parts of talcum powder into the mixture B obtained in the step (2), and stirring and dispersing for 20-30 min until the whole system is uniformly mixed to obtain a mixture C.
(4) And 4, step 4: adding 7-12 parts of silicon dioxide dispersion liquid and 1.5-2 parts of isobutyl acrylate into a third reaction container, heating to 50-60 ℃, stirring for 15min, adding 5-10 parts of allyl phosphate and 5-15 parts of aluminum silicate fiber into the reaction container, keeping the temperature at 50-60 ℃, stirring for 30min, adding the mixture C obtained in the step (3), stirring and dispersing for 30-40 min, and mixing the whole system uniformly to obtain a mixture D.
(5) And 5: and (4) adding 20-30 parts of copper pyrithione, 10-20 parts of film forming agent, 1.6-2 parts of dispersing agent and 1-5 parts of polyethyleneimine into the mixture D obtained in the step (4), and stirring and dispersing for 10-15 min under the stirring condition of 600-800 rpm to obtain the coating. The prepared coating is sprayed on the surface of a metal material which is easy to corrode by using an electrostatic spraying gun to form a coating, and the coating has the advantages of good adhesiveness, difficult shedding, strong contact adhesive force with the metal surface and good comprehensive performance.
The above contents are only examples and illustrations of the invention, and the coating prepared by the method is used on the surface of metal, has high glossiness, high temperature resistance, good surface hardness, high corrosion resistance, good adhesiveness, difficult shedding, strong contact adhesive force with the metal surface, high paint film hardness of the coating, good coloring effect, difficult agglomeration, is suitable for surface treatment decoration of iron, common alloy, metal easy to rust and the like, and has good comprehensive performance. Various modifications, additions and substitutions for the specific embodiments described may occur to those skilled in the art without departing from the scope of the invention or exceeding the scope of the claims.

Claims (8)

1. A coating, characterized by: the paint comprises the following raw materials, by weight, 10-20 parts of a mixture A, 40-45 parts of titanium dioxide sol, 15-20 parts of isocyanate, 30-40 parts of polyethylene glycol, 10-15 parts of a cosolvent, 5-8 parts of talcum powder, 7-12 parts of a silicon dioxide dispersion liquid, 5-15 parts of aluminum silicate fiber, 1.5-2 parts of isobutyl acrylate, 5-10 parts of allyl phosphate, 20-30 parts of copper pyrithione, 10-20 parts of a film forming agent, 1.6-2 parts of a dispersing agent and 1-5 parts of polyethyleneimine.
2. The coating of claim 1, wherein: the mixture A is 1.5-2 parts of polyoxypropylene glycerol ether, 10-15 parts of silica sol, 10-20 parts of deionized water and 10-20 parts of isobutyl acrylate, and is prepared by stirring and dispersing in a container at normal temperature for 20-25 min.
3. A coating according to claim 1, wherein: the mixture A is 1.5-2 parts of polyoxypropylene glycerol ether, 10-15 parts of silica sol, 10-20 parts of deionized water, 10-20 parts of isobutyl acrylate and 5-10 parts of conductive mica powder, static electricity is introduced into an insulating plastic barrel, and stirring and dispersing are carried out for 20-25 min, so that the conductive mica powder is prepared.
4. A coating according to claim 3, wherein: and introducing static electricity into the mixture A at 5000-15000 volts.
5. A coating according to claim 1, wherein: the titanium dioxide sol is nano titanium dioxide sol.
6. A coating according to claim 1, wherein: the cosolvent is any one of sodium salicylate and p-aminobenzoic acid.
7. A preparation method of the coating comprises the following steps:
(1) step 1: adding 1.5-2 parts of polyoxypropylene glycerol ether, 10-15 parts of silica sol, 10-20 parts of deionized water and 10-20 parts of isobutyl acrylate into a first reaction container, and stirring and dispersing for 20-25 min at normal temperature to obtain a mixture A for later use;
(2) step 2: adding 40-45 parts of titanium dioxide sol, 15-20 parts of isocyanate and 30-40 parts of polyethylene glycol into a second reaction container, heating to 50 ℃, stirring for 30min, adding the mixture A obtained in the step (1), and stirring and dispersing for 30-40 min to obtain a mixture B;
(3) and step 3: adding 10-15 parts of cosolvent and 5-8 parts of talcum powder into the step 2, stirring and dispersing for 20-30 min until the whole system is uniformly mixed to obtain a mixture C;
(4) and 4, step 4: adding 7-12 parts of silicon dioxide dispersion liquid and 1.5-2 parts of isobutyl acrylate into a third reaction container, heating to 50-60 ℃, stirring for 15min, adding 5-10 parts of allyl phosphate and 5-15 parts of aluminum silicate fiber into the reaction container, keeping the temperature at 50-60 ℃, stirring for 30min, adding the mixture C obtained in the step (3), stirring and dispersing for 30-40 min, and mixing the whole system uniformly to obtain a mixture D;
(5) and 5: and (4) adding 20-30 parts of copper pyrithione, 10-20 parts of film forming agent, 1.6-2 parts of dispersing agent and 1-5 parts of polyethyleneimine into the mixture D obtained in the step (4), and stirring and dispersing for 10-15 min under the stirring condition of 600-800 rpm to obtain the coating.
8. A preparation method of the coating comprises the following steps: (1) step 1: adding 1.5-2 parts of polyoxypropylene glycerol ether, 10-15 parts of silica sol, 10-20 parts of deionized water, 10-20 parts of isobutyl acrylate and 5-10 parts of conductive mica powder into a first reaction container, introducing static electricity into an insulating plastic barrel, and stirring and dispersing for 20-25 min to obtain a mixture A for later use;
(2) step 2: adding 40-45 parts of titanium dioxide sol, 15-20 parts of isocyanate and 30-40 parts of polyethylene glycol into a second reaction container, heating to 50 ℃, stirring for 30min, adding the mixture A obtained in the step (1), and stirring and dispersing for 30-40 min to obtain a mixture B;
(3) and step 3: adding 10-15 parts of cosolvent and 5-8 parts of talcum powder into the step 2, stirring and dispersing for 20-30 min until the whole system is uniformly mixed to obtain a mixture C;
(4) and 4, step 4: adding 7-12 parts of silicon dioxide dispersion liquid and 1.5-2 parts of isobutyl acrylate into a third reaction container, heating to 50-60 ℃, stirring for 15min, adding 5-10 parts of allyl phosphate and 5-15 parts of aluminum silicate fiber into the reaction container, keeping the temperature at 50-60 ℃, stirring for 30min, adding the mixture C obtained in the step (3), stirring and dispersing for 30-40 min, and mixing the whole system uniformly to obtain a mixture D;
(5) and 5: and (4) adding 20-30 parts of copper pyrithione, 10-20 parts of film forming agent, 1.6-2 parts of dispersing agent and 1-5 parts of polyethyleneimine into the mixture D obtained in the step (4), and stirring and dispersing for 10-15 min under the stirring condition of 600-800 rpm to obtain the coating.
CN202210129002.5A 2022-02-11 2022-02-11 Coating and preparation method thereof Pending CN114410140A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202210129002.5A CN114410140A (en) 2022-02-11 2022-02-11 Coating and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202210129002.5A CN114410140A (en) 2022-02-11 2022-02-11 Coating and preparation method thereof

Publications (1)

Publication Number Publication Date
CN114410140A true CN114410140A (en) 2022-04-29

Family

ID=81279764

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202210129002.5A Pending CN114410140A (en) 2022-02-11 2022-02-11 Coating and preparation method thereof

Country Status (1)

Country Link
CN (1) CN114410140A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114686068A (en) * 2022-05-18 2022-07-01 岑卫康 Strong-protective coating and preparation method thereof

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106634096A (en) * 2016-12-16 2017-05-10 苏州富艾姆工业设备有限公司 Water-based nanometer coating and preparation process thereof
CN107868579A (en) * 2017-12-16 2018-04-03 苏州赛斯德工程设备有限公司 A kind of Environmental Protective Water-paint
CN112159623A (en) * 2020-09-28 2021-01-01 成都玉龙化工有限公司 High-temperature-resistant coating and preparation method thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106634096A (en) * 2016-12-16 2017-05-10 苏州富艾姆工业设备有限公司 Water-based nanometer coating and preparation process thereof
CN107868579A (en) * 2017-12-16 2018-04-03 苏州赛斯德工程设备有限公司 A kind of Environmental Protective Water-paint
CN112159623A (en) * 2020-09-28 2021-01-01 成都玉龙化工有限公司 High-temperature-resistant coating and preparation method thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114686068A (en) * 2022-05-18 2022-07-01 岑卫康 Strong-protective coating and preparation method thereof

Similar Documents

Publication Publication Date Title
RU2182161C2 (en) Covering composition, backing with cover, method of backing preparing, method of preparing covering composition
CN101619195B (en) High-temperature resistant workshop primer and preparation process thereof
CN101613559A (en) Hydrophilic nano zinc based composite coating
CN101792635A (en) Strong-pressure resisting water-based insulting paint for electric steel and preparation method thereof
CN111349923B (en) Chromium-free environment-friendly passivation treating fluid for zinc layer surface and preparation method and application thereof
CN114181616B (en) Chromium-free low-temperature curing water-based zinc-aluminum coating and preparation method and application thereof
JP2014031505A (en) Rust preventive coating material, rust preventive coating film and rust preventive laminated coating film
CN114410140A (en) Coating and preparation method thereof
JP2013505116A (en) Use of coatings that cure at room temperature
CN109880484A (en) A kind of water-base epoxy thickness slurry anti-decaying paint and its preparation method and application
CN101629045A (en) High solid metal inner cavity anticorrosive paint and production method thereof
CN103173049A (en) Compound modifier-containing anticorrosive coating
CN108329801B (en) Environment-friendly integrated waterproof coating and preparation method thereof
CN108409932A (en) A kind of preparation method of modified epoxy and its application in anticorrosive paint
CN112608647A (en) Water-based inorganic nano high-temperature-resistant ceramic anticorrosive paint and application method thereof
CN108299878A (en) A kind of anti-forging graphene oxide protective coating of aqueous medium temperature and preparation method thereof
CN110951361A (en) Anticorrosive and sweat-resistant coating and preparation method and application thereof
JPS6328942B2 (en)
JP7329599B2 (en) Heat-resistant paint composition, heat-resistant coating film, substrate with heat-resistant coating film, and method for producing the same
CN103173050A (en) Ferrocene-containing anticorrosive paint
CN112592616A (en) Composite reinforced anticorrosive coating composition containing graphene and nano titanium
CN114686068A (en) Strong-protective coating and preparation method thereof
CN111647334A (en) Laminated scaly heavy-duty anticorrosive paint and preparation method thereof
JPS60235871A (en) Primary rust-resisting paint composition
JPH0446932A (en) Resin composition for zinc-rich paint

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
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20220429