CN109593454A - A kind of polyurethane coating and its preparation method and application - Google Patents

A kind of polyurethane coating and its preparation method and application Download PDF

Info

Publication number
CN109593454A
CN109593454A CN201811572619.4A CN201811572619A CN109593454A CN 109593454 A CN109593454 A CN 109593454A CN 201811572619 A CN201811572619 A CN 201811572619A CN 109593454 A CN109593454 A CN 109593454A
Authority
CN
China
Prior art keywords
component
polyurethane coating
graphene oxide
agent
modified graphene
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
CN201811572619.4A
Other languages
Chinese (zh)
Other versions
CN109593454B (en
Inventor
姚永健
荣仲尼
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 Good State Graphene New Mstar Technology Ltd
Original Assignee
Guangdong Good State Graphene New Mstar Technology Ltd
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 Good State Graphene New Mstar Technology Ltd filed Critical Guangdong Good State Graphene New Mstar Technology Ltd
Priority to CN201811572619.4A priority Critical patent/CN109593454B/en
Publication of CN109593454A publication Critical patent/CN109593454A/en
Application granted granted Critical
Publication of CN109593454B publication Critical patent/CN109593454B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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
    • C09D175/00Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04Polyurethanes
    • 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
    • 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
    • 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
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00Properties
    • C08L2201/08Stabilised against heat, light or radiation or oxydation

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)
  • Paints Or Removers (AREA)

Abstract

The present invention provides a kind of polyurethane coating and its preparation method and application, the polyurethane coating includes component A and B component, and the component A includes the following component of weight percent: solvent 10-30%, dicarboxylic acid esters 2-8%, polyalcohol 45-75%, modified graphene oxide 0.5-4%, titanium dioxide 15-35%, polyamide wax 0.1-1%, bentonite 0.1-1% and 0.5-2% auxiliary agent;The B component is isocyanate curing agent.The present invention is by being added modified graphene oxide into component A, and cooperate the other compositions of component A, to be combined with B component, prepare polyurethane coating, so that the paint adhesion being prepared is high, acid resistance, alkali resistance, salt spray resistance are very excellent, for outdoor anticorrosion of steel structure, with excellent Corrosion Protection, and safety and environmental protection.

Description

A kind of polyurethane coating and its preparation method and application
Technical field
The invention belongs to technical field of coatings, it is related to a kind of polyurethane coating and its preparation method and application.
Background technique
Metal is easy to be corroded under various complex environments, in order to prevent the corrosion of metal structure, and on its surface, coating is anti- Rotten coating can efficiently solve this problem, should guarantee anticorrosive paint adhesive force, weatherability, in terms of have There is excellent performance, guarantees coating safety and environmental protection again.
108384429 A of CN discloses a kind of polyurethane coating, and the polyurethane coating prepares raw material and group subpackage It includes: equal three nitrogen of azoformic acid dibenzyl ester 0.25g, polytetrahydrofuran ether glycol 72g, hexamethylene diisocyanate 18g, hexahydro Borine 0.68g, methyl ethyl ketone 8.8g, modified manganese hypophosphite 1g, 4- Carboxybenzeneboronic acid 3.2g, N- hydroxy thiosuccinimide 3.5g, triethylamine 7.8g and water 70g obtain the polyurethane coating of fire-retardant, waterproof Yu low VOC, however the invention does not make Polyurethane coating adhesive force, weatherability, in terms of have larger improvement.
Therefore, in this field, it is expected that developing, a kind of adhesive force is high, and acid resistance, alkali resistance, salt spray resistance are very excellent Polyurethane coating.
Summary of the invention
In view of the deficiencies of the prior art, the purpose of the present invention is to provide a kind of polyurethane coating and preparation method thereof and answer With polyurethane coating adhesive force of the invention is high, has excellent acid resistance, alkali resistance and salt spray resistance, has good Corrosion-resisting function, and safety and environmental protection.
To achieve this purpose, the present invention adopts the following technical scheme:
On the one hand, the present invention provides a kind of polyurethane coating, and the polyurethane coating includes component A and B component;
The component A includes the following component of weight percent:
The B component is isocyanate curing agent.
In the present invention, by being added modified graphene oxide into component A, and cooperate the other compositions of component A, with It is combined with B component, prepares polyurethane coating, so that the paint adhesion being prepared is high, acid resistance, alkali resistance, salt fog resistance It can be very excellent.
In the present invention, in the component A, solvent is preferably the mixed solvent of butyl ester and dimethylbenzene.
Preferably, in the component A, solvent be mass ratio be 2:1-5:1 (such as 2:1,2.3:1,2.5:1,2.8:1,3: 1,3.3:1,3.5:1,3.8:1,4:1,4.3:1,4.5:1,4.8:1 or 5:1) butyl ester and dimethylbenzene mixed solution, preferably The mass ratio of butyl ester and dimethylbenzene is 3:1.
In the present invention, in the component A, the dosage of solvent can for 10%, 13%, 15%, 18%, 20%, 23%, 25%, 28% or 30%.
In the present invention, the dosage of the dicarboxylic acid esters can for 2%, 2.5%, 2.8%, 3%, 3.3%, 3.5%, 3.8%, 4%, 4.5%, 4.8%, 5%, 5.5%, 5.8%, 6%, 6.3%, 6.5%, 6.8%, 7%, 7.3%, 7.5%, 7.8% or 8%.
In the present invention, the polyalcohol is acrylic acid modified polyol resin.
In the present invention, the dosage of the polyalcohol can for 45%, 48%, 50%, 53%, 55%, 58%, 60%, 63%, 65%, 68%, 70%, 73% or 75%.
In the present invention, the modified graphene oxide is silane coupler modified graphene oxide.
Preferably, the silane coupling agent is the silane coupling agent with active amino, preferably gamma-aminopropyl-triethoxy silicon Alkane or silane coupling agent Z-6011.
Preferably, the modified graphene oxide is prepared by the following method: graphene oxide being dispersed to organic molten In agent, and silane coupling agent is added in the graphene oxide dispersion obtained backward, reacts, obtain the modified graphite oxide Alkene.
Preferably, the organic solvent is the mixed solution or n,N-Dimethylformamide of dimethylbenzene and n-butanol.
Preferably, the mode of the dispersion is ultrasonic disperse.
Preferably, the time of the ultrasonic disperse be 10-40min, such as 10min, 13min, 15min, 18min, 20min, 25min, 28min, 30min, 35min, 38min or 40min.
In the present invention, in graphene oxide dispersion, relative to 1g graphene oxide, the dosage of the organic solvent is 10-100mL, for example, 10mL, 15mL, 20mL, 25mL, 30mL, 35mL, 40mL, 45mL, 50mL, 55mL, 60mL, 65mL, 70mL, 75mL, 80mL, 85mL, 90mL, 95mL or 100mL.
Preferably, the temperature of the reaction is 70-90 DEG C, such as 70 DEG C, 73 DEG C, 75 DEG C, 78 DEG C, 80 DEG C, 83 DEG C, 85 DEG C, 88 DEG C or 90 DEG C.
Preferably, the reaction carries out under stiring.
Preferably, the time of the reaction be 5-24 hours, such as 5 hours, 7 hours, 9 hours, 10 hours, 12 hours, 14 hours, 16 hours, 18 hours, 20 hours, 22 hours or 24 hours.
In the present invention, the dosage of the modified graphene oxide be 0.5%, 0.8%, 1%, 1.3%, 1.5%, 1.8%, 2%, 2.3%, 2.5%, 2.8%, 3%, 3.2%, 3.5%, 3.8% or 4%.
In the present invention, the dosage of the titanium dioxide can for 15%, 18%, 20%, 23%, 25%, 28%, 30%, 33% or 35%.
In the present invention, the dosage of the polyamide wax can for 0.1%, 0.2%, 0.3%, 0.4%, 0.5%, 0.6%, 0.7%, 0.8%, 0.9% or 1%.
In the present invention, the bentonitic dosage can for 0.1%, 0.2%, 0.3%, 0.4%, 0.5%, 0.6%, 0.7%, 0.8%, 0.9% or 1%.
In the present invention, the auxiliary dosage can be 0.5%, 0.8%, 1%, 1.3%, 1.5%, 1.8% or 2%.
Preferably, the auxiliary agent includes levelling agent, dispersing agent and defoaming agent.
Preferably, the isocyanate curing agent is toluene di-isocyanate(TDI) (TDI), '-diphenylmethane diisocyanate (MDI) or in isophorone diisocyanate (IPDI) any one or at least two combination.
Preferably, the mass ratio of component A and B component is 3:1-9:1, such as 3:1,3.5:1,4:1,4.5:1,5:1,5.5: 1,6:1,6.5:1,7:1,7.5:1,8:1,8.3:1,8.5:1,8.8:1 or 9:1, preferably 4:1.
In the present invention, the preparation method of the polyurethane coating will form the ingredient mixing of component A, then by component A It is mixed with B component, normal temperature cure, 25 DEG C curing time 7 days or more (such as 7 days, 8 days, 9 days, 10 days etc.), obtains the poly- ammonia Ester paint.
On the other hand, the present invention provides the applications in polyurethane coating as described above outdoors anticorrosion of steel structure.
Preferably, the polyurethane coating is used for outdoor anticorrosion of steel structure as finishing coat.
Polyurethane coating of the invention can be used in outdoor anticorrosion of steel structure, have good acid resistance, alkali resistance, salt tolerant Mist performance, adhesive force is high, and corrosion resistance is good.It can be applied anti-to enhance together with the modified anti-corrosion primer of graphene Corrosive nature.
Compared with the existing technology, the invention has the following advantages:
The present invention cooperates the other compositions of component A by being added modified graphene oxide into component A, with B group Divide and combine, prepare polyurethane coating, so that the paint adhesion being prepared is high, acid resistance, alkali resistance, salt spray resistance are non- Chang Youyi, adhesive force can reach 13MPa or more, and acid resistance and alkali resistance can reach 2000h or more, and humidity resistance reaches 2200h or more, water resistance reach 5000h or more, have qualified temperature-change resistance energy and UV resistance, for outdoor steel knot Structure anti-corrosion has excellent Corrosion Protection, and safety and environmental protection.
Specific embodiment
The technical scheme of the invention is further explained by means of specific implementation.Those skilled in the art should be bright , the described embodiments are merely helpful in understanding the present invention, should not be regarded as a specific limitation of the invention.
Embodiment 1
In the present embodiment, a kind of polyurethane coating is provided, the polyurethane coating includes the component A that mass ratio is 4:1 And B component;
The component A includes the following component of weight percent:
The B component is isocyanate curing agent, that is, toluene di-isocyanate(TDI).
Wherein the modified graphene oxide is silane coupler modified graphene oxide, and preparation method is as follows:
500mL is dispersed by the 6g graphene oxide after drying, in DMF (n,N-Dimethylformamide) solvent, ultrasound point 30min is dissipated, graphene oxide dispersion is made, then, is added 100g KH550 (gamma-aminopropyl-triethoxy-silane), heating It to 80 DEG C, stirs 12 hours, after the reaction was completed, cleans 3 times with deionized water and be centrifugated, product is carried out at vacuum drying Reason, obtains the modified graphene oxide.
The polyurethane coating the preparation method comprises the following steps: will form component A ingredient mix, then component A and B component are mixed Close, normal temperature cure, 25 DEG C curing time 7 days, obtain the polyurethane coating.
Embodiment 2
In the present embodiment, a kind of polyurethane coating is provided, the polyurethane coating includes the component A that mass ratio is 4:1 And B component;
The component A includes the following component of weight percent:
The B component is isocyanate curing agent, that is, toluene di-isocyanate(TDI).
Wherein the modified graphene oxide is silane coupler modified graphene oxide, and preparation method is as follows:
180mL is dispersed by the 6g graphene oxide after drying, in DMF (n,N-Dimethylformamide) solvent, ultrasound point 25min is dissipated, graphene oxide dispersion is made, then, is added 100g KH550 (gamma-aminopropyl-triethoxy-silane), heating It to 70 DEG C, stirs 20 hours, after the reaction was completed, cleans 3 times with deionized water and be centrifugated, product is carried out at vacuum drying Reason, obtains the modified graphene oxide.
The polyurethane coating the preparation method comprises the following steps: will form component A ingredient mix, then component A and B component are mixed Close, normal temperature cure, 25 DEG C curing time 7 days, obtain the polyurethane coating.
Embodiment 3
In the present embodiment, a kind of polyurethane coating is provided, the polyurethane coating includes the component A that mass ratio is 9:1 And B component;
The component A includes the following component of weight percent:
The B component is isocyanate curing agent, that is, toluene di-isocyanate(TDI).
Wherein the modified graphene oxide is silane coupler modified graphene oxide, and preparation method is as follows:
300mL is dispersed by the 6g graphene oxide after drying, in DMF (n,N-Dimethylformamide) solvent, ultrasound point 40min is dissipated, graphene oxide dispersion is made, then, is added 100g KH550 (gamma-aminopropyl-triethoxy-silane), heating It to 900 DEG C, stirs 5 hours, after the reaction was completed, cleans 3 times with deionized water and be centrifugated, product is carried out at vacuum drying Reason, obtains the modified graphene oxide.
The polyurethane coating the preparation method comprises the following steps: will form component A ingredient mix, then component A and B component are mixed Close, normal temperature cure, 25 DEG C curing time 9 days, obtain the polyurethane coating.
Embodiment 4
In the present embodiment, a kind of polyurethane coating is provided, the polyurethane coating includes the component A that mass ratio is 5:1 And B component;
The component A includes the following component of weight percent:
The B component is isocyanate curing agent, that is, isophorone diisocyanate.
Wherein the modified graphene oxide is silane coupler modified graphene oxide, and preparation method is as follows:
600mL is dispersed by the 6g graphene oxide after drying, in DMF (n,N-Dimethylformamide) solvent, ultrasound point 10min is dissipated, graphene oxide dispersion is made, then, is added 100g KH550 (gamma-aminopropyl-triethoxy-silane), heating It to 85 DEG C, stirs 18 hours, after the reaction was completed, cleans 3 times with deionized water and be centrifugated, product is carried out at vacuum drying Reason, obtains the modified graphene oxide.
The polyurethane coating the preparation method comprises the following steps: will form component A ingredient mix, then component A and B component are mixed Close, normal temperature cure, 25 DEG C curing time 7 days, obtain the polyurethane coating.
Embodiment 5
In the present embodiment, a kind of polyurethane coating is provided, the polyurethane coating includes the component A that mass ratio is 6:1 And B component;
The component A includes the following component of weight percent:
The B component is isocyanate curing agent, that is, '-diphenylmethane diisocyanate.
Wherein the modified graphene oxide is silane coupler modified graphene oxide, and preparation method is as follows:
400mL is dispersed by the 6g graphene oxide after drying, in DMF (n,N-Dimethylformamide) solvent, ultrasound point 20min is dissipated, graphene oxide dispersion is made, then, is added 100g KH550 (gamma-aminopropyl-triethoxy-silane), heating It to 75 DEG C, stirs 24 hours, after the reaction was completed, cleans 3 times with deionized water and be centrifugated, product is carried out at vacuum drying Reason, obtains the modified graphene oxide.
The polyurethane coating the preparation method comprises the following steps: will form component A ingredient mix, then component A and B component are mixed Close, normal temperature cure, 25 DEG C curing time 8 days, obtain the polyurethane coating.
Comparative example 1
Difference from Example 1 is only that the mass ratio of component A and B component is 2:1.
Comparative example 2
Difference from Example 1 is only that the mass ratio of component A and B component is 10:1.
Comparative example 3
Difference from Example 1 is only that in component A that, without containing modified graphene oxide, titanium dioxide dosage is 23%.
Polyurethane coating prepared by embodiment and comparative example is coated on steel structure surface as finishing coat and is used for anti-corrosion, it is right Its salt spray resistance, resistance to acid and alkali, resistance to salt water, water resistance and adhesion performance are measured, and testing standard and index are wanted Ask as shown in table 1.
Table 1
It is as shown in table 2 to the actual performance test data of the coating of embodiment 1-5 and comparative example 1-3.
Table 2
The Applicant declares that the present invention is explained by the above embodiments polyurethane coating of the invention and preparation method thereof and Using, but the present invention is not limited to the above embodiments, that is, does not mean that the present invention must rely on above-described embodiment and could implement. It should be clear to those skilled in the art, any improvement in the present invention, equivalent the replacing to each raw material of product of the present invention It changes and the addition of auxiliary element, the selection of concrete mode etc., all of which fall within the scope of protection and disclosure of the present invention.

Claims (10)

1. a kind of polyurethane coating, which is characterized in that the polyurethane coating includes component A and B component;
The component A includes the following component of weight percent:
The B component is isocyanate curing agent.
2. polyurethane coating according to claim 1, which is characterized in that in the component A, solvent is preferably butyl ester and two The mixed solvent of toluene;
Preferably, in the component A, solvent is the mixed solution of the butyl ester that mass ratio is 2:1-5:1 and dimethylbenzene, preferably butyl ester Mass ratio with dimethylbenzene is 3:1.
3. polyurethane coating according to claim 1 or 2, which is characterized in that the polyalcohol is acrylic acid modified more First alcohol resin.
4. polyurethane coating according to any one of claim 1-3, which is characterized in that the modified graphene oxide is Silane coupler modified graphene oxide;
Preferably, the silane coupling agent be the silane coupling agent with active amino, preferably gamma-aminopropyl-triethoxy-silane or Silane coupling agent Z-6011.
5. polyurethane coating described in any one of -4 according to claim 1, which is characterized in that the modified graphene oxide by Following method is prepared: in the graphene oxide dispersion that graphene oxide is dispersed in organic solvent, and is obtained backward Silane coupling agent is added, reaction obtains the modified graphene oxide;
Preferably, the organic solvent is the mixed solution or n,N-Dimethylformamide of dimethylbenzene and n-butanol;
Preferably, the mode of the dispersion is ultrasonic disperse;
Preferably, the time of the ultrasonic disperse is 10-40min.
6. polyurethane coating according to claim 5, which is characterized in that in graphene oxide dispersion, relative to 1g oxygen Graphite alkene, the dosage of the organic solvent are 10-100mL;
Preferably, the temperature of the reaction is 70-90 DEG C;
Preferably, the reaction carries out under stiring;
Preferably, the time of the reaction is 5-24 hours.
7. polyurethane coating according to claim 1 to 6, which is characterized in that the auxiliary agent include levelling agent, Dispersing agent and defoaming agent;
Preferably, the isocyanate curing agent is toluene di-isocyanate(TDI), '-diphenylmethane diisocyanate or isophorone two In isocyanates any one or at least two combination.
8. polyurethane coating described in any one of -7 according to claim 1, which is characterized in that the mass ratio of component A and B component For 3:1-9:1.
9. the preparation method of polyurethane coating according to claim 1 to 8, which is characterized in that the preparation side Method are as follows: the ingredient for forming component A is mixed, then component A is mixed, normal temperature cure with B component, is conserved 7 days or more at 25 DEG C, Obtain the polyurethane coating.
10. polyurethane coating according to claim 1 to 8 application in anticorrosion of steel structure outdoors;
Preferably, the polyurethane coating is used for outdoor anticorrosion of steel structure as finishing coat.
CN201811572619.4A 2018-12-21 2018-12-21 Polyurethane coating and preparation method and application thereof Active CN109593454B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201811572619.4A CN109593454B (en) 2018-12-21 2018-12-21 Polyurethane coating and preparation method and application thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201811572619.4A CN109593454B (en) 2018-12-21 2018-12-21 Polyurethane coating and preparation method and application thereof

Publications (2)

Publication Number Publication Date
CN109593454A true CN109593454A (en) 2019-04-09
CN109593454B CN109593454B (en) 2021-01-12

Family

ID=65963421

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201811572619.4A Active CN109593454B (en) 2018-12-21 2018-12-21 Polyurethane coating and preparation method and application thereof

Country Status (1)

Country Link
CN (1) CN109593454B (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110804328A (en) * 2019-11-05 2020-02-18 徐州汉通电子科技有限公司 Polyurethane coating for electronic element
CN113087679A (en) * 2020-01-08 2021-07-09 万华化学集团股份有限公司 Polyisocyanate curing agent with low free monomer, preparation method, coating composition and application
CN114163916A (en) * 2021-12-23 2022-03-11 重庆品涂新材料科技有限公司 Waterproof paint and production method thereof
CN114736597A (en) * 2022-03-31 2022-07-12 吉林大学 Bionic porous cavitation-resistant coating and coating
CN116904103A (en) * 2023-06-16 2023-10-20 龙蟒大地农业有限公司 Low-carbon environment-friendly functionalized graphene oxide polyurethane coating and preparation method thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5876464A (en) * 1981-10-30 1983-05-09 Mitui Toatsu Chem Inc Pressurized one-package polyurethane coating and coating method using the same
JPS6136995B2 (en) * 1977-11-22 1986-08-21 Dainippon Toryo Kk
US20100075139A1 (en) * 2008-09-25 2010-03-25 Fujifilm Corporation Electroconductive material and method of producing the same
CN104356860A (en) * 2014-10-29 2015-02-18 中国科学院宁波材料技术与工程研究所 Epoxy resin-oxidized graphene composite coating and application method thereof
CN108864906A (en) * 2018-04-17 2018-11-23 国网浙江省电力有限公司电力科学研究院 Antifouling antistatic anti-corrosion nano compound polyurethane paint and preparation method thereof

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6136995B2 (en) * 1977-11-22 1986-08-21 Dainippon Toryo Kk
JPS5876464A (en) * 1981-10-30 1983-05-09 Mitui Toatsu Chem Inc Pressurized one-package polyurethane coating and coating method using the same
US20100075139A1 (en) * 2008-09-25 2010-03-25 Fujifilm Corporation Electroconductive material and method of producing the same
CN104356860A (en) * 2014-10-29 2015-02-18 中国科学院宁波材料技术与工程研究所 Epoxy resin-oxidized graphene composite coating and application method thereof
CN108864906A (en) * 2018-04-17 2018-11-23 国网浙江省电力有限公司电力科学研究院 Antifouling antistatic anti-corrosion nano compound polyurethane paint and preparation method thereof

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110804328A (en) * 2019-11-05 2020-02-18 徐州汉通电子科技有限公司 Polyurethane coating for electronic element
CN113087679A (en) * 2020-01-08 2021-07-09 万华化学集团股份有限公司 Polyisocyanate curing agent with low free monomer, preparation method, coating composition and application
CN114163916A (en) * 2021-12-23 2022-03-11 重庆品涂新材料科技有限公司 Waterproof paint and production method thereof
CN114736597A (en) * 2022-03-31 2022-07-12 吉林大学 Bionic porous cavitation-resistant coating and coating
CN114736597B (en) * 2022-03-31 2022-08-30 吉林大学 Bionic porous cavitation-resistant coating and coating
CN116904103A (en) * 2023-06-16 2023-10-20 龙蟒大地农业有限公司 Low-carbon environment-friendly functionalized graphene oxide polyurethane coating and preparation method thereof

Also Published As

Publication number Publication date
CN109593454B (en) 2021-01-12

Similar Documents

Publication Publication Date Title
CN109593454A (en) A kind of polyurethane coating and its preparation method and application
CN104372317B (en) A kind of watery anti-corrosion resin
CN107709390B (en) Carbodiimide-based aqueous resin crosslinking agent
CN104559617B (en) A kind of application type aqueous dual-component fluorocarbon coating and its preparation and application
CN109761834A (en) A kind of preparation method and application of the dispersible polyaspartic ester resin of water and aqueous carbamide paint
CN109651922A (en) A kind of aqueous polyurethane toughening water borne epoxy resin anticorrosive paint and preparation method
JP5632607B2 (en) Protective covering material for concrete structure and method for protecting concrete structure
CN105199511B (en) A kind of stainless steel ground varnish and its preparation method and application
CN103627003B (en) A kind of fluorine silicon graftomer Graft Epoxy Resin and preparation method thereof
CN105385334A (en) Preparation method of two-component aqueous polyurethane transparent thermal conductive coating
CN109486384A (en) A kind of polyurea type Polyaspartic Ester-Based Coatings feedstock composition, from its coating and its preparation method and application
CN108912870A (en) A kind of selfreparing anti-corrosion outdoor building graphene coating and preparation method
CN110437723B (en) Multi-effect antifouling paint and construction method thereof
CN105218752A (en) The preparation method of the polyurethane-acrylate water dispersion of epoxy-silicone resin modification and water-based epoxy zinc-rich primer
CN104140754A (en) Solvent-free polyurethane coating and preparation method thereof
CN103146296B (en) Transparent water-based acrylate modified epoxy polyurethane food container inner paint
CN110305564A (en) Two coating water-based anticorrosive paints of one kind and application
CN108441105A (en) A kind of aspartate high-strength weather-resistant waterproof finishing coat and preparation method thereof
CN109575225B (en) Graphene oxide modified curing agent, polyurethane coating, and preparation method and application thereof
CN101368051A (en) Water-soluble band tape paint and method of producing the same
CN110330880A (en) A kind of anticorrosive paint, preparation method and application method
CN111087841A (en) Anticorrosive coating for surface of magnesium alloy substrate
CN113025132A (en) Water-based organic silicon modified fluorocarbon wind power blade coating and preparation method thereof
CN105778046B (en) A kind of aqueous polyurethane and its preparation method and application
CN109852173A (en) Graphene is modified silicone acrylic emulsion anti-corrosion anti-static coatings

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