CN107502129A - Preparation method with epoxy radicals acrylic resin modified epoxy anticorrosive paint - Google Patents

Preparation method with epoxy radicals acrylic resin modified epoxy anticorrosive paint Download PDF

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Publication number
CN107502129A
CN107502129A CN201611103831.7A CN201611103831A CN107502129A CN 107502129 A CN107502129 A CN 107502129A CN 201611103831 A CN201611103831 A CN 201611103831A CN 107502129 A CN107502129 A CN 107502129A
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CN
China
Prior art keywords
acrylic resin
preparation
epoxy
anticorrosive paint
initiator
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
CN201611103831.7A
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Chinese (zh)
Inventor
王耀斌
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Shaanxi Gaoxin Industry Co Ltd
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Shaanxi Gaoxin Industry Co Ltd
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Filing date
Publication date
Application filed by Shaanxi Gaoxin Industry Co Ltd filed Critical Shaanxi Gaoxin Industry Co Ltd
Priority to CN201611103831.7A priority Critical patent/CN107502129A/en
Publication of CN107502129A publication Critical patent/CN107502129A/en
Pending legal-status Critical Current

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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
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10Esters
    • C08F220/12Esters of monohydric alcohols or phenols
    • C08F220/14Methyl esters, e.g. methyl (meth)acrylate
    • CCHEMISTRY; METALLURGY
    • 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

Abstract

The present invention relates to synthetic resin and plastics arts, and in particular to a kind of preparation method with epoxy radicals acrylic resin modified epoxy anticorrosive paint.Preparation method with epoxy radicals acrylic resin modified epoxy anticorrosive paint, comprises the following steps:Methyl methacrylate, butyl acrylate are taken, mercaptan mixes in beaker, takes initiator solution standby;196.8g butyl acetates are added into 1000mL three-necked flasks, open condensed water and 3.0g initiator solutions and 30.0g mix monomers are added after being warming up to 80 DEG C, interruption adds mix monomer and initiator, is incubated 1 h and adds 3.0g initiators, 2h is incubated again, and acrylic resin is made;Acrylic resin is mixed with epoxy resin, and compounds rust resisting pigment, filler preparation coating.The ply adhesion of modified epoxy anticorrosive paint of the present invention is higher.

Description

Preparation method with epoxy radicals acrylic resin modified epoxy anticorrosive paint
Technical field
The present invention relates to synthetic resin and plastics arts, and in particular to a kind of band epoxy radicals acrylic resin is modified ring The preparation method of oxygen resin anti-corrosive paint.
Background technology
Due to the influence of ocean harsh and unforgiving environments, metal is easily corroded.Prevent one of the most frequently used measure of metal erosion It is exactly brushing anticorrosive paint, and in anticorrosive paint, anti-corrosive paint of epoxy resin is one of kind being most widely used.Epoxy Resin contains the functional groups such as hydroxyl, epoxy radicals, and the space structure formed after being crosslinked with curing agent such as amine, acid anhydrides, esters is determined Having determined it has excellent adhesive strength, resistance to corrosive chemicals, insulating properties and mechanical strength;But there is also all for epoxy resin More drawbacks(Such as due to phenyl ring be present in epoxy resin, cause its weatherability and ultraviolet resistance poor;Anti-corrosive paint of epoxy resin is consolidated Re-coating layer ply adhesion reduces after change, is easily caused the peeling of coating interlayer;The internal stress of epoxy resin is larger etc.), therefore pure epoxy The application of resin anti-corrosive paint is restricted.In recent years, substantial amounts of work has been done in modification of many scholars to epoxy resin, main It is divided into physical modification and chemical modification.Acrylic resin is because its excellent weatherability, pliability and good recoatability are in thing It is widely used during reason is modified.The ply adhesion of anti-corrosive paint of epoxy resin can be improved by being incorporated into epoxy resin.
The content of the invention
A kind of the present invention is directed to propose preparation method with epoxy radicals acrylic resin modified epoxy anticorrosive paint.
Technical program of the present invention lies in:
Preparation method with epoxy radicals acrylic resin modified epoxy anticorrosive paint, comprises the following steps:
(1)The synthesis of acrylic resin:
Methyl methacrylate, butyl acrylate are taken, mercaptan mixes in beaker, takes initiator solution standby;To 1 000 mL Add 196.8 g butyl acetates in three-necked flask, open condensed water and added after being warming up to 80 DEG C 3.0 g initiator solutions and 30.0 g mix monomers, interruption add mix monomer and initiator, are incubated 1 h and add 3.0 g initiators, then are incubated 2 h, make Obtain acrylic resin;
(2)Coating preparation:
Acrylic resin is mixed with epoxy resin, and compounds rust resisting pigment, filler preparation coating.
Described epoxy resin and the mass ratio of acrylic resin are 9: 1.
Described methyl methacrylate quality is 150.2 g, and butyl acrylate quality is 96.0 g, and mercaptan quality is 2.40 g。
Described initiator solution is dissolved in 50.0 g butyl acetates for 0.4 g azodiisobutyronitriles and obtained.
It is to draw every 15 min, 38.3 g mix monomers of addition and 8.0 g that described interruption, which adds mix monomer and initiator, Send out agent.
The technical effects of the invention are that:
The present invention has synthesized band epoxy radicals acrylic resin using radical polymerization, and polymerization, and polymer completely occurs for monomer Band epoxy radicals;With the increase of initiator and chain-transferring agent dosage, the viscosity with epoxy radicals acrylic resin declines;With pure epoxy Resin anti-corrosive paint is compared, and the ply adhesion of modified epoxy anticorrosive paint is higher.
Embodiment
Preparation method with epoxy radicals acrylic resin modified epoxy anticorrosive paint, comprises the following steps:
Embodiment 1
(1)The synthesis of acrylic resin:
Methyl methacrylate, butyl acrylate are taken, mercaptan mixes in beaker, takes initiator solution standby;To 1 000 mL Add 196.8 g butyl acetates in three-necked flask, open condensed water and added after being warming up to 80 DEG C 3.0 g initiator solutions and 30.0 g mix monomers, interruption add mix monomer and initiator, are incubated 1 h and add 3.0 g initiators, then are incubated 2 h, make Obtain acrylic resin;
(2)Coating preparation:
Acrylic resin is mixed with epoxy resin, and compounds rust resisting pigment, filler preparation coating.
Wherein, the mass ratio of described epoxy resin and acrylic resin is 9: 1.Described methyl methacrylate quality For 150.2 g, butyl acrylate quality is 96.0 g, and mercaptan quality is 2.40 g.Described initiator solution is 0.4 g even Nitrogen bis-isobutyronitrile is dissolved in 50.0 g butyl acetates and obtained.Described interruption adds mix monomer and initiator to add every 15 min Enter 38.3 g mix monomers and 8.0 g initiators.
Embodiment 2
(1)The synthesis of acrylic resin:
Methyl methacrylate, butyl acrylate are taken, mercaptan mixes in beaker, takes initiator solution standby;To 1 000 mL 197.5g butyl acetates are added in three-necked flask, open condensed water and add after being warming up to 85 DEG C 3.0 g initiator solutions and 30.0 g mix monomers, interruption add mix monomer and initiator, are incubated 1 h and add 3.0 g initiators, then are incubated 2 h, make Obtain acrylic resin;
(2)Coating preparation:
Acrylic resin is mixed with epoxy resin, and compounds rust resisting pigment, filler preparation coating.
Wherein, the mass ratio of described epoxy resin and acrylic resin is 10: 1.Described methyl methacrylate matter It is 96.0 g to measure as 150.2 g, butyl acrylate quality, and mercaptan quality is 2.40 g.Described initiator solution is 0.4 g Azodiisobutyronitrile is dissolved in 50.0 g butyl acetates and obtained.It is every 15 min that described interruption, which adds mix monomer and initiator, Add 38.3 g mix monomers and 8.0 g initiators.
Embodiment 3
(1)The synthesis of acrylic resin:
Methyl methacrylate, butyl acrylate are taken, mercaptan mixes in beaker, takes initiator solution standby;To 1 000 mL 197.5g butyl acetates are added in three-necked flask, open condensed water and add after being warming up to 85 DEG C 3.0 g initiator solutions and 30.0 g mix monomers, interruption add mix monomer and initiator, are incubated 1 h and add 3.0 g initiators, then are incubated 2 h, make Obtain acrylic resin;
(2)Coating preparation:
Acrylic resin is mixed with epoxy resin, and compounds rust resisting pigment, filler preparation coating.
Wherein, the mass ratio of described epoxy resin and acrylic resin is 9.5: 1.Described methyl methacrylate matter It is 96.0 g to measure as 150.2 g, butyl acrylate quality, and mercaptan quality is 2.40 g.Described initiator solution is 0.4 g Azodiisobutyronitrile is dissolved in 50.0 g butyl acetates and obtained.It is every 15 min that described interruption, which adds mix monomer and initiator, Add 38.3 g mix monomers and 8.0 g initiators.

Claims (5)

1. the preparation method with epoxy radicals acrylic resin modified epoxy anticorrosive paint, it is characterised in that:Including following step Suddenly:
(1)The synthesis of acrylic resin:
Methyl methacrylate, butyl acrylate are taken, mercaptan mixes in beaker, takes initiator solution standby;To 1 000 mL Add 196.8 g butyl acetates in three-necked flask, open condensed water and added after being warming up to 80 DEG C 3.0 g initiator solutions and 30.0 g mix monomers, interruption add mix monomer and initiator, are incubated 1 h and add 3.0 g initiators, then are incubated 2 h, make Obtain acrylic resin;
(2)Coating preparation:
Acrylic resin is mixed with epoxy resin, and compounds rust resisting pigment, filler preparation coating.
2. the preparation method according to claim 1 with epoxy radicals acrylic resin modified epoxy anticorrosive paint, its It is characterised by:Described epoxy resin and the mass ratio of acrylic resin are 9: 1.
3. the preparation method according to claim 1 with epoxy radicals acrylic resin modified epoxy anticorrosive paint, its It is characterised by:Described methyl methacrylate quality is 150.2 g, and butyl acrylate quality is 96.0 g, and mercaptan quality is 2.40 g。
4. the preparation method according to claim 1 with epoxy radicals acrylic resin modified epoxy anticorrosive paint, its It is characterised by:Described initiator solution is dissolved in 50.0 g butyl acetates for 0.4 g azodiisobutyronitriles and obtained.
5. the preparation method according to claim 1 with epoxy radicals acrylic resin modified epoxy anticorrosive paint, its It is characterised by:It is to add 38.3 g mix monomers and 8.0 g every 15 min that described interruption, which adds mix monomer and initiator, Initiator.
CN201611103831.7A 2016-12-05 2016-12-05 Preparation method with epoxy radicals acrylic resin modified epoxy anticorrosive paint Pending CN107502129A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201611103831.7A CN107502129A (en) 2016-12-05 2016-12-05 Preparation method with epoxy radicals acrylic resin modified epoxy anticorrosive paint

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201611103831.7A CN107502129A (en) 2016-12-05 2016-12-05 Preparation method with epoxy radicals acrylic resin modified epoxy anticorrosive paint

Publications (1)

Publication Number Publication Date
CN107502129A true CN107502129A (en) 2017-12-22

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CN201611103831.7A Pending CN107502129A (en) 2016-12-05 2016-12-05 Preparation method with epoxy radicals acrylic resin modified epoxy anticorrosive paint

Country Status (1)

Country Link
CN (1) CN107502129A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114149532A (en) * 2021-12-07 2022-03-08 中国海洋大学 Acrylic resin containing epoxy group and ethylene ureido group, preparation method and application thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114149532A (en) * 2021-12-07 2022-03-08 中国海洋大学 Acrylic resin containing epoxy group and ethylene ureido group, preparation method and application thereof

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Application publication date: 20171222