CN107652736B - A kind of epoxy ultraviolet-curing paint - Google Patents

A kind of epoxy ultraviolet-curing paint Download PDF

Info

Publication number
CN107652736B
CN107652736B CN201710995477.1A CN201710995477A CN107652736B CN 107652736 B CN107652736 B CN 107652736B CN 201710995477 A CN201710995477 A CN 201710995477A CN 107652736 B CN107652736 B CN 107652736B
Authority
CN
China
Prior art keywords
parts
epoxy
added
bisphenol
necked flask
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.)
Active
Application number
CN201710995477.1A
Other languages
Chinese (zh)
Other versions
CN107652736A (en
Inventor
陈建伟
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.)
ZHANGJIAGANG HENGYE RESINS Co.,Ltd.
Original Assignee
Zhejiang Timber New Material Co 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 Zhejiang Timber New Material Co Ltd filed Critical Zhejiang Timber New Material Co Ltd
Priority to CN201710995477.1A priority Critical patent/CN107652736B/en
Publication of CN107652736A publication Critical patent/CN107652736A/en
Application granted granted Critical
Publication of CN107652736B publication Critical patent/CN107652736B/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
    • 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
    • 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
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Emergency Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Paints Or Removers (AREA)
  • Epoxy Resins (AREA)

Abstract

The invention discloses a kind of epoxy ultraviolet-curing paints, it is composed of the following components according to parts by weight: 60-80 parts of bisphenol A type epoxy resin, 15-26 parts of bisphenol-A epoxy resin, 20-30 parts of borosilicate modified epoxy, 20-35 parts of glycerin triglycidyl ether, 5-15 parts of ethoxylated trimethylolpropane triacrylate, 5-8 parts of triaryl matte hexafluoro antimonate, 1-2 parts of azodiisobutyronitrile, 1-2 parts of benzoin isopropyl ether, 2-5 parts of fluorinated acrylate levelling agent.The invention has the following beneficial effects: energy needed for (1) photocuring is low;(2) resin system is lower;(3) hardness of film height, high and low temperature resistance and good toughness after solidifying.

Description

A kind of epoxy ultraviolet-curing paint
Technical field
The present invention relates to a kind of coating, more particularly, to a kind of epoxy ultraviolet-curing paint.
Background technique
In the past few years, ultraviolet-curing paint fibre coating, CD coating/DVD adhesive, credit card, timber, Very rapid development is suffered from beverage can, food packaging, journal surface, medical instrument and automobile industry.Ultraviolet light solidification Coating possesses huge market potential, and the ratio in entire coating products increases year by year.Ultraviolet-curing paint master It to be made of oligomer, monomer, photoinitiator and auxiliary agent.The cured key reaction course of ultraviolet light be caused by radiation it is light-initiated Agent is decomposed, and is generated living radical and is caused monomer/oligomer polymerization crosslinking.
Resin used in ultraviolet light solidification at present is just substantially acrylic resin and two kinds of epoxy resin, middle ring Oxygen resin is the organic compound referred in molecule containing two or more epoxy groups, in addition to individual, they opposite Molecular mass is not high.The molecular structure of epoxy resin be in strand contain active epoxy group be its feature, epoxy Group can be located at the end of strand, centre or circlewise structure.Due to containing active epoxy group in molecular structure, make They can be crosslinked with a plurality of types of curing agent reacts and forms the insoluble high polymer with three-dimensional reticular structure.All point High-molecular compound in minor structure containing epoxy group is referred to as epoxy resin.Epoxy resin after solidification has good object Reason, chemical property, it has excellent adhesive strength to the surface of metal and nonmetallic materials, and dielectric properties are good, and deformation is received Shrinkage is small, and product size stability is good, and hardness is high, and flexibility is preferable, to alkali and most of solvent-stable, thus is widely used in National defence, each department of national economy are poured, impregnate, the purposes such as lamination material, bonding agent, coating.
However energy used in epoxies ultraviolet-curing paint photocuring on the market is higher at present, obtains after solidification Although film hardness is higher, it is more crisp, can not impact resistance, high and low temperature resistance, and its not resistant not resistant to water.Such as one kind exists A kind of UV photocuring sanding primer reported in Chinese patent literature, application publication number are 105315734 A of CN, the hair It is bright to disclose a kind of UV photocuring sanding primer, which is characterized in that be made of the raw material of following weight percents: bisphenol A-type Epoxy resin E-42 60-65%, benzophenone 2-3%, TPGDA 20-30%, n-butanol 10-15%, modified diamond dust 2- 3%, nanosized SiO_2 1-2%, defoaming agent 0.5-0.8%, dispersing agent 0.4-0.6%.UV photocuring sanding primer of the present invention is low Volatilization, low smell, environmental pollution are small;With preferable hardness;It with good grinability, is easily sanded, while also having one Fixed fillibility;Curing rate is fast, high production efficiency;Normal temperature cure is suitble to a variety of substrates;Energy saving, energy consumption is approximately tradition The 1/5 of coating;The performance indicator of the organic solvents various aspects such as coating is wear-resisting, acid and alkali-resistance, salt spray resistance, resistance to gasoline is very high, especially It is that its paint film is plentiful, gloss is especially prominent.But its there is also more deficiencies, although such as its have preferable hardness, its Main resin is that its heat resistance of bisphenol A type epoxy resin and toughness is not high, is unable to satisfy daily use.
Summary of the invention
The present invention be in order to overcome photocureable coating not high-low temperature resistant in the prior art, the coating property obtained after solidification compared with It is crisp, it is not resistant to water intolerant to greasy dirt the problem of, provide one kind can high-low temperature resistant, the coating property obtained after solidification is tough and tensile, water-fast resistance to A kind of epoxy ultraviolet-curing paint of greasy dirt.
To achieve the goals above, the invention adopts the following technical scheme:
A kind of epoxy ultraviolet-curing paint, it is composed of the following components according to parts by weight: bisphenol A type epoxy resin 60- 80 parts, 15-26 parts of bisphenol-A epoxy resin, 20-30 parts of borosilicate modified epoxy, glycerin triglycidyl ether 20- 35 parts, 5-15 parts of ethoxylated trimethylolpropane triacrylate, 5-8 parts of triaryl matte hexafluoro antimonate, azo two is different 1-2 parts of butyronitrile, 1-2 parts of benzoin isopropyl ether, 2-5 parts of fluorinated acrylate levelling agent.
Preferably, composed of the following components according to parts by weight: 65-75 parts of bisphenol A type epoxy resin, hydrogenated bisphenol A 18-25 parts of type epoxy resin, 20-30 parts of borosilicate modified epoxy, 25-30 parts of glycerin triglycidyl ether, ethoxylation 5-12 parts of trimethylolpropane trimethacrylate, 5-8 parts of triaryl matte hexafluoro antimonate, 1-2 parts of azodiisobutyronitrile are rested in peace Fragrant isopropyl ether 1-2 parts, 2-5 parts of fluorinated acrylate levelling agent.
Preferably, composed of the following components according to parts by weight: 70 parts of bisphenol A type epoxy resin, hydrogenated bisphenol A type ring 22 parts of oxygen resin, 28 parts of borosilicate modified epoxy, 30 parts of glycerin triglycidyl ether, ethoxylated trimethylolpropane three 10 parts of acrylate, 6 parts of triaryl matte hexafluoro antimonate, 2 parts of azodiisobutyronitrile, 2 parts of benzoin isopropyl ether, fluorine-containing propene 4 parts of acid esters levelling agent.
Bisphenol A type epoxy resin and bisphenol-A epoxy resin have the advantages that hardness is high, intensity is high, but its toughness It is poor, it is added to after borosilicate modified epoxy, can aid in promotion finally through the toughness of resin material.Further, since For borosilicate modified epoxy due to containing Si-O-B structure in its main chain, high and low temperature resistance is superior, being capable of reinforced resin material The high and low temperature resistance of material.Simultaneously because it is added to glycerin triglycidyl ether, three propylene of ethoxylated trimethylolpropane The resin material of the low viscosities such as acid esters facilitates the viscosity for reducing whole system, and the addition of fluorinated acrylate levelling agent can Guarantee the levelling of final resin, and due to its internal fluorine atom, makes the surface Waterproofing/oilproofing object after the completion of solidifying.In the present invention It is acted synergistically using triaryl matte hexafluoro antimonate, azodiisobutyronitrile and benzoin isopropyl ether three different initiators, It can effectively ensure that the completeness of photocuring and reduce the energy of photocuring.
The borosilicate modified epoxy the preparation method is as follows:
(a) there-necked flask takes 10 parts of boron under -20-0 DEG C and nitrogen atmosphere with constant pressure funnel according to parts by weight Acid, 48-52 parts of triethylamines, 50 parts of organic solvents are added in there-necked flask and are sufficiently stirred, and are then added in constant pressure funnel 45-50 parts of dimethylchlorosilanes and 50 parts of organic solvents, are slowly added dropwise into there-necked flask, the reaction was continued 3-5 after being added dropwise Hour, it is filtered to remove the triethylamine hydrochloride of generation after reaction, filtrate washes 3 times, organic solvent is removed under reduced pressure, obtains three (dimethyl silicon substrate) borate.
(b) there-necked flask matches constant pressure funnel, under 80-100 DEG C and atmosphere, by three (diformazan obtained in step (a) Base silicon substrate) 50 parts of borate, 50 parts, 0.05-0.2 parts platiniferous 2% of toluene platinum catalyst be added in there-necked flask, then in perseverance It presses and 75-80 parts of allyl glycidyl ethers, 30 parts of toluene is added in dropping funel, be then slowly dropped in three-necked flask, drip The reaction was continued after adding 4-6 hours, and 1-3 parts of active carbons are added after reaction and stir 0.5-2 hours, solvent is evaporated off in filtering And low-boiling-point substance, obtain borosilicate modified epoxy.
Preferably, the organic solvent in the step (a) is tetrahydrofuran, anhydrous ether, methylene chloride, n-hexane One of.
Preferably, the platinum catalyst of the step (b) is isopropyl alcohol solution of chloroplatinic acid, Karst catalyst, allyl One of base silicon (oxygen) alkane platinum complex.
Preferably, the ultraviolet-curing paint the preparation method is as follows: each component is added according to parts by weight Into container, then container is put into baking oven and increases temperature to 55-65 DEG C, heats 30-90 minutes, then takes out high-speed stirred Dispersion 0.5-3 hours, then ultrasonic disperse 0.5-2 hours, obtains epoxy ultraviolet-curing paint.
Therefore, the invention has the following beneficial effects: energy needed for (1) photocuring is low;(2) resin system viscosity is lower; (3) hardness of film height, high and low temperature resistance and good toughness after solidifying.
Technical solution of the present invention is made to further describe explanation below by specific embodiment.
If saying that the raw material of use is raw material commonly used in the art without specified otherwise, in the embodiment of the present invention, implement Method employed in example, is the conventional method of this field.
Embodiment 1
A kind of epoxy ultraviolet-curing paint, it is composed of the following components according to parts by weight: bisphenol A type epoxy resin 60 Part, 15 parts of bisphenol-A epoxy resin, 20 parts of borosilicate modified epoxy, 20 parts of glycerin triglycidyl ether, ethyoxyl Change 5 parts of trimethylolpropane trimethacrylate, 5 parts of triaryl matte hexafluoro antimonate, 1 part of azodiisobutyronitrile, benzoin isobutyl 1 part of propyl ether, 2 parts of fluorinated acrylate levelling agent.
The borosilicate modified epoxy the preparation method is as follows:
(a) there-necked flask match constant pressure funnel, under -20 DEG C and nitrogen atmosphere, take according to parts by weight 10 parts of boric acid, 48 parts of triethylamines, 50 parts of tetrahydrofurans are added in there-necked flask and are sufficiently stirred, and 45 part two is then added in constant pressure funnel Methylchlorosilane and 50 parts of tetrahydrofurans, are slowly added dropwise into there-necked flask, and the reaction was continued 3 hours after being added dropwise, reaction knot The triethylamine hydrochloride of generation is filtered to remove after beam, filtrate washes 3 times, organic solvent is removed under reduced pressure, obtains three (dimethyl-silicons Base) borate.
(b) there-necked flask matches constant pressure funnel, under 80 DEG C and nitrogen atmosphere, by three (diformazan obtained in step (a) Base silicon substrate) 50 parts of borate, 50 parts, 0.05 part platiniferous 2% of toluene isopropyl alcohol solution of chloroplatinic acid be added in there-necked flask, then 75 parts of allyl glycidyl ethers, 30 parts of toluene are added in constant pressure funnel, are then slowly dropped in there-necked flask, drop The reaction was continued after adding 4 hours, and 1 part of active carbon is added after reaction and stirs 0.5 hour, filtering, and solvent and low is evaporated off Object is boiled, borosilicate modified epoxy is obtained.
The ultraviolet-curing paint the preparation method is as follows: each component is added in container according to parts by weight, Then container is put into baking oven and increases temperature to 55 DEG C, heated 30 minutes, then take out high-speed stirred dispersion 0.5 hour, so Ultrasonic disperse 0.5 hour afterwards obtains epoxy ultraviolet-curing paint.
Embodiment 2
A kind of epoxy ultraviolet-curing paint, it is composed of the following components according to parts by weight: bisphenol A type epoxy resin 80 Part, 26 parts of bisphenol-A epoxy resin, 30 parts of borosilicate modified epoxy, 35 parts of glycerin triglycidyl ether, ethyoxyl Change 15 parts of trimethylolpropane trimethacrylate, 8 parts of triaryl matte hexafluoro antimonate, 2 parts of azodiisobutyronitrile, benzoin isobutyl 2 parts of propyl ether, 5 parts of fluorinated acrylate levelling agent.
The borosilicate modified epoxy the preparation method is as follows:
(a) there-necked flask takes 10 parts of boric acid, 52 under 0 DEG C and nitrogen atmosphere with constant pressure funnel according to parts by weight Part triethylamine, 50 parts of anhydrous ethers are added in there-necked flask and are sufficiently stirred, and 50 parts of diformazans are then added in constant pressure funnel Base chlorosilane and 50 parts of anhydrous ethers, are slowly added dropwise into there-necked flask, and the reaction was continued 5 hours after being added dropwise, and reaction terminates It is filtered to remove the triethylamine hydrochloride of generation afterwards, filtrate washes 3 times, organic solvent is removed under reduced pressure, obtains three (dimethyl silicon substrates) Borate.
(b) there-necked flask matches constant pressure funnel, under 100 DEG C and nitrogen atmosphere, by three (two obtained in step (a) Methylsilyl) 50 parts of borate, 50 parts, 0.2 part platiniferous 2% of toluene Karst catalyst be added in there-necked flask, then exist 80 parts of allyl glycidyl ethers, 30 parts of toluene are added in constant pressure funnel, are then slowly dropped in there-necked flask, knot is added dropwise The reaction was continued after beam 6 hours, and 3 parts of active carbons are added after reaction and stir 2 hours, filtering is evaporated off solvent and low-boiling-point substance, obtains To borosilicate modified epoxy.
The ultraviolet-curing paint coating the preparation method is as follows: each component is added to container according to parts by weight In, then container is put into baking oven and increases temperature to 65 DEG C, is heated 90 minutes, then takes out high-speed stirred dispersion 3 hours, so Ultrasonic disperse 2 hours afterwards obtain epoxy ultraviolet-curing paint.
Embodiment 3
A kind of epoxy ultraviolet-curing paint, it is composed of the following components according to parts by weight: bisphenol A type epoxy resin 65 Part, 18 parts of bisphenol-A epoxy resin, 20 parts of borosilicate modified epoxy, 25 parts of glycerin triglycidyl ether, ethyoxyl Change 5 parts of trimethylolpropane trimethacrylate, 5 parts of triaryl matte hexafluoro antimonate, 1 part of azodiisobutyronitrile, benzoin isobutyl 1 part of propyl ether, 2 parts of fluorinated acrylate levelling agent.
The borosilicate modified epoxy the preparation method is as follows:
(a) there-necked flask match constant pressure funnel, under -10 DEG C and nitrogen atmosphere, take according to parts by weight 10 parts of boric acid, 50 parts of triethylamines, 50 parts of methylene chloride are added in there-necked flask and are sufficiently stirred, and 47 part two is then added in constant pressure funnel Methylchlorosilane and 50 parts of methylene chloride, are slowly added dropwise into there-necked flask, and the reaction was continued 4 hours after being added dropwise, reaction knot The triethylamine hydrochloride of generation is filtered to remove after beam, filtrate washes 3 times, organic solvent is removed under reduced pressure, obtains three (dimethyl-silicons Base) borate.
(b) there-necked flask matches constant pressure funnel, under 95 DEG C and nitrogen atmosphere, by three (diformazan obtained in step (a) Base silicon substrate) 50 parts of borate, 50 parts, 0.1 part platiniferous 2% of toluene Karst catalyst be added in there-necked flask, then in perseverance It presses and 75 parts of allyl glycidyl ethers, 30 parts of toluene is added in dropping funel, be then slowly dropped in there-necked flask, completion of dropwise addition The reaction was continued afterwards 5 hours, and 2 parts of active carbons are added after reaction and stir 1 hour, filtering is evaporated off solvent and low-boiling-point substance, obtains Borosilicate modified epoxy.
The ultraviolet-curing paint the preparation method is as follows: each component is added in container according to parts by weight, Then container is put into baking oven and increases temperature to 60 DEG C, heated 60 minutes, then take out high-speed stirred dispersion 2 hours, then Ultrasonic disperse 1 hour, obtain epoxy ultraviolet-curing paint.
Embodiment 4
A kind of epoxy ultraviolet-curing paint, it is composed of the following components according to parts by weight: bisphenol A type epoxy resin 75 Part, 25 parts of bisphenol-A epoxy resin, 30 parts of borosilicate modified epoxy, 30 parts of glycerin triglycidyl ether, ethyoxyl Change 12 parts of trimethylolpropane trimethacrylate, 8 parts of triaryl matte hexafluoro antimonate, 2 parts of azodiisobutyronitrile, benzoin isobutyl 2 parts of propyl ether, 5 parts of fluorinated acrylate levelling agent.
The borosilicate modified epoxy the preparation method is as follows:
(a) there-necked flask match constant pressure funnel, under -5 DEG C and nitrogen atmosphere, take according to parts by weight 10 parts of boric acid, 48 parts of triethylamines, 50 parts there is n-hexane to be added in there-necked flask to be sufficiently stirred, 48 part two is then added in constant pressure funnel Methylchlorosilane and 50 parts of n-hexanes, are slowly added dropwise into there-necked flask, and the reaction was continued 3 hours after being added dropwise, and reaction terminates It is filtered to remove the triethylamine hydrochloride of generation afterwards, filtrate washes 3 times, organic solvent is removed under reduced pressure, obtains three (dimethyl silicon substrates) Borate.
(b) there-necked flask matches constant pressure funnel, under 85 DEG C and nitrogen atmosphere, by three (diformazan obtained in step (a) Base silicon substrate) 50 parts of borate, 50 parts, 0.15 part platiniferous 2% of toluene allyl silicon (oxygen) alkane platinum complex be added to there-necked flask In, 80 parts of allyl glycidyl ethers, 30 parts of toluene are then added in constant pressure funnel, are then slowly dropped to there-necked flask In, the reaction was continued after completion of dropwise addition 4 hours, and 1.5 parts of active carbons are added after reaction and stir 0.5 hour, solvent is evaporated off in filtering And low-boiling-point substance, obtain borosilicate modified epoxy.
The ultraviolet-curing paint the preparation method is as follows: each component is added in container according to parts by weight, Then container is put into baking oven and increases temperature to 65 DEG C, heated 30 minutes, then take out high-speed stirred dispersion 0.5 hour, so Ultrasonic disperse 2 hours afterwards obtain epoxy ultraviolet-curing paint.
Embodiment 5
A kind of epoxy ultraviolet-curing paint, it is composed of the following components according to parts by weight: bisphenol A type epoxy resin 70 Part, 22 parts of bisphenol-A epoxy resin, 28 parts of borosilicate modified epoxy, 30 parts of glycerin triglycidyl ether, ethyoxyl Change 10 parts of trimethylolpropane trimethacrylate, 6 parts of triaryl matte hexafluoro antimonate, 2 parts of azodiisobutyronitrile, benzoin isobutyl 2 parts of propyl ether, 4 parts of fluorinated acrylate levelling agent.
The borosilicate modified epoxy the preparation method is as follows:
(a) there-necked flask match constant pressure funnel, under -20 DEG C and nitrogen atmosphere, take according to parts by weight 10 parts of boric acid, 48 parts of triethylamines, 50 parts of anhydrous ethers are added in there-necked flask and are sufficiently stirred, and 50 part two is then added in constant pressure funnel Methylchlorosilane and 50 parts of anhydrous ethers, are slowly added dropwise into there-necked flask, and the reaction was continued 3-5 hours after being added dropwise, reaction After be filtered to remove the triethylamine hydrochloride of generation, filtrate washes 3 times, organic solvent is removed under reduced pressure, obtains three (dimethyl-silicons Base) borate.
(b) there-necked flask matches constant pressure funnel, under 100 DEG C and nitrogen atmosphere, by three (two obtained in step (a) Methylsilyl) 50 parts of borate, 50 parts, 0.2 part platiniferous 2% of toluene Karst catalyst be added in there-necked flask, then exist 75 parts of allyl glycidyl ethers, 30 parts of toluene are added in constant pressure funnel, are then slowly dropped in there-necked flask, knot is added dropwise The reaction was continued after beam 4 hours, and 3 parts of active carbons are added after reaction and stir 2 hours, filtering is evaporated off solvent and low-boiling-point substance, obtains To borosilicate modified epoxy.
The ultraviolet-curing paint coating the preparation method is as follows: each component is added to container according to parts by weight In, then container is put into baking oven and increases temperature to 60 DEG C, is heated 45 minutes, then takes out high-speed stirred dispersion 3 hours, so Ultrasonic disperse 1.5 hours afterwards obtain epoxy ultraviolet-curing paint.
Performance test
The resin combination of embodiment 1-5 is passed through into photocuring, the film after photocuring passes through performance evaluation, specific item Part is as follows, the result is as follows:
Pencil hardness: pencil hardness test is by standard GB/T/T6739-2006 test, and bear a heavy burden 500g
Glass transition temperature: DSC temperature range is 20-180 DEG C, 5 DEG C/min of heating rate.
Thermal decomposition temperature: TGA temperature range is 50-800 DEG C, 10 DEG C/min of heating rate.
Surface contact angle: GB/T23764-2009 standard testing is pressed in water contact angle test.
Cubical contraction: the measurement work formula of cubical contraction is as follows
Wherein, η is that resin UV solidifies front and back cubical contraction, ρsFor the density for solidifying exemplar, ρlTo solidify preceding resin liquid Density.
Water absorption rate: after the resin after the completion of solidification is placed in 100 DEG C of oven drying 5h, its weight m is surveyed0, then by batten It is vertically arranged in the beaker for filling distilled water, distilled water liquid level is higher than batten, and removes the bubble on print.After 7 days, sample is taken out Piece surveys its weight m after drying moisture1

Claims (6)

1. a kind of epoxy ultraviolet-curing paint, characterized in that composed of the following components according to parts by weight: bisphenol type epoxy 60-80 parts of resin, 15-26 parts of bisphenol-A epoxy resin, 20-30 parts of borosilicate modified epoxy, glycerine three shrink sweet Oily ether 20-35 parts, 5-15 parts of ethoxylated trimethylolpropane triacrylate, 5-8 parts of triaryl matte hexafluoro antimonate, it is even 1-2 parts of nitrogen bis-isobutyronitrile, 1-2 parts of benzoin isopropyl ether, 2-5 parts of fluorinated acrylate levelling agent;
The borosilicate modified epoxy the preparation method is as follows:
(a) there-necked flask match constant pressure funnel, under -20-0 DEG C and nitrogen atmosphere, take according to parts by weight 10 parts of boric acid, 48-52 parts of triethylamines, 50 parts of organic solvents are added in there-necked flask and are sufficiently stirred, and 45- is then added in constant pressure funnel 50 parts of dimethylchlorosilanes and 50 parts of organic solvents, are slowly added dropwise into there-necked flask, and the reaction was continued after being added dropwise, and 3-5 is small When, it is filtered to remove the triethylamine hydrochloride of generation after reaction, filtrate washes 3 times, organic solvent is removed under reduced pressure, obtains three (dimethyl silicon substrate) borate;
(b) there-necked flask matches constant pressure funnel, under 80-100 DEG C and nitrogen atmosphere, by three (diformazan obtained in step (a) Base silicon substrate) 50 parts of borate, 50 parts, 0.05-0.2 parts platiniferous 2% of toluene platinum catalyst be added in there-necked flask, then in perseverance It presses and 75-80 parts of allyl glycidyl ethers, 30 parts of toluene is added in dropping funel, be then slowly dropped in three-necked flask, drip The reaction was continued after adding 4-6 hours, and 1-3 parts of active carbons are added after reaction and stir 0.5-2 hours, solvent is evaporated off in filtering And low-boiling-point substance, obtain borosilicate modified epoxy.
2. a kind of epoxy ultraviolet-curing paint according to claim 1, characterized in that according to parts by weight by with the following group It is grouped as: 65-75 parts of bisphenol A type epoxy resin, 18-25 parts of bisphenol-A epoxy resin, borosilicate modified epoxy 20- 30 parts, 25-30 parts of glycerin triglycidyl ether, 5-12 parts of ethoxylated trimethylolpropane triacrylate, triaryl matte 5-8 parts of hexafluoro antimonate, 1-2 parts of azodiisobutyronitrile, 1-2 parts of benzoin isopropyl ether, fluorinated acrylate levelling agent 2-5 Part.
3. a kind of epoxy ultraviolet-curing paint according to claim 1, characterized in that according to parts by weight by with the following group It is grouped as: 70 parts of bisphenol A type epoxy resin, 22 parts of bisphenol-A epoxy resin, 28 parts of borosilicate modified epoxy, the third three 30 parts of alcohol triglycidyl ether, 10 parts of ethoxylated trimethylolpropane triacrylate, triaryl matte hexafluoro antimonate 6 Part, 2 parts of azodiisobutyronitrile, 2 parts of benzoin isopropyl ether, 4 parts of fluorinated acrylate levelling agent.
4. a kind of epoxy ultraviolet-curing paint according to claim 1, characterized in that having in the step (a) Solvent is one of tetrahydrofuran, anhydrous ether, methylene chloride, n-hexane.
5. a kind of epoxy ultraviolet-curing paint according to claim 1, characterized in that the platinum of the step (b) is urged Agent is one of isopropyl alcohol solution of chloroplatinic acid, Karst catalyst, Allyl Siloxane platinum complex.
6. a kind of epoxy ultraviolet-curing paint described according to claim 1 ~ any one of 3, characterized in that the purple Outer photocureable coating the preparation method is as follows: each component is added in container according to parts by weight, container is then put into baking Temperature is increased in case to 55-65 DEG C, is heated 30-90 minutes, is then taken out high-speed stirred and is dispersed 0.5-3 hours, then ultrasound is divided It dissipates 0.5-2 hours, obtains ultraviolet-curing paint.
CN201710995477.1A 2017-10-23 2017-10-23 A kind of epoxy ultraviolet-curing paint Active CN107652736B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201710995477.1A CN107652736B (en) 2017-10-23 2017-10-23 A kind of epoxy ultraviolet-curing paint

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201710995477.1A CN107652736B (en) 2017-10-23 2017-10-23 A kind of epoxy ultraviolet-curing paint

Publications (2)

Publication Number Publication Date
CN107652736A CN107652736A (en) 2018-02-02
CN107652736B true CN107652736B (en) 2019-09-10

Family

ID=61119296

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201710995477.1A Active CN107652736B (en) 2017-10-23 2017-10-23 A kind of epoxy ultraviolet-curing paint

Country Status (1)

Country Link
CN (1) CN107652736B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108690355B (en) * 2018-06-26 2021-05-14 浙江三元电子科技有限公司 Flexible heat conduction sheet and preparation method thereof

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104761994A (en) * 2015-04-10 2015-07-08 南昌航空大学 Preparation method of photocuring organic silicon modified epoxy resin paint film

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104761994A (en) * 2015-04-10 2015-07-08 南昌航空大学 Preparation method of photocuring organic silicon modified epoxy resin paint film

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
有机硅硼改性环氧树脂胶粘剂的研制;杨凤等;《中国胶粘剂》;20080731;第17卷(第7期);第28-31页

Also Published As

Publication number Publication date
CN107652736A (en) 2018-02-02

Similar Documents

Publication Publication Date Title
CN103073934B (en) Ultraviolet curing anti-fingerprint coating for acrylic and composite material base material thereof
CN102712783B (en) Plastic substrates having a scratch-resistant coating, in particular housings of electronic devices, having high transparency, method for the production thereof, and use thereof
CN103031034B (en) A kind of white finish paint optical curing of UV coating and preparation method thereof
CN102977758B (en) UV (ultraviolet) photocured water-based fluorine-containing polyurethane latex film and preparation method thereof
CN101531839A (en) Silicon- and fluorine-containing epoxy (meth) acrylate UV-curing composite coating and preparation method thereof
CN102061127A (en) UV-solidified nanometer inorganic/organic hybrid painting preparation method and application thereof
CN107207906A (en) For the resin combination of hard conating and including hard coat film of its cured form as coating
CN112048077B (en) Castor oil-based aqueous photocuring nonionic emulsion and preparation method and application thereof
CN110272679A (en) Hyperbranched super-amphiphobic anticorrosive paint of ultraviolet-cured paint phenolic group and preparation method thereof
CN107652736B (en) A kind of epoxy ultraviolet-curing paint
CN109735144A (en) A kind of photocuring POSS/ fluorohydrocarbon radical siloxane modified polyacrylate coating composition and its application
CN103443149A (en) Lipophilic, highly branched polymer, and photopolymerizable composition containing the same
CN109679511A (en) A kind of rapid curing glue film and preparation method thereof
CN113683723A (en) Fluorosilicone modified resin for antifouling, preparation and aqueous antifouling coating thereof
Li et al. Preparation of siloxymethyl-modified silicone acrylate prepolymers with UV/moisture dual curability for applications in anti-smudge and anti-fingerprint coatings
CN106187953B (en) A kind of cationic polymerization monomer and synthesis and application
CN115141504A (en) Maleic anhydride polybutadiene modified ultraviolet-curing polyacrylate coating composition and preparation method thereof
CN110669222B (en) Optically transparent material and preparation method thereof, polymer film and manufacturing method thereof
CN104635285B (en) High-stiffness coated reflecting film and preparation method thereof
JP2013064038A (en) Transparent film-forming coating material, and base material with transparent film
JP5596920B2 (en) Paint for forming transparent film and substrate with transparent film
CN115181442B (en) Anti-yellowing UV skin-feel paint
CN107629639B (en) A kind of ultraviolet-curing paint
CN110527388A (en) A kind of silicone glass liquid ultraviolet-curing paint
CN106188120A (en) A kind of bifunctionality acrylate monomer of silicone-containing structure and preparation method thereof

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
TR01 Transfer of patent right
TR01 Transfer of patent right

Effective date of registration: 20201207

Address after: 515636 No. 1, Lane 2, Dongtougongqian District, Stork Chao Sancun, Longhu Town, Chaoan District, Chaozhou City, Guangdong Province

Patentee after: Li Yanling

Address before: 313200 Zhejiang city of Huzhou province Deqing County Wukang Ring Road No. 190

Patentee before: ZHEJIANG TIMBER NEW MATERIAL Co.,Ltd.

TR01 Transfer of patent right
TR01 Transfer of patent right

Effective date of registration: 20210430

Address after: Zhangjiagang Hengye special resin Co., Ltd

Patentee after: ZHANGJIAGANG HENGYE RESINS Co.,Ltd.

Address before: 515636 No.1, Lane 2, District 1, dongtougongqian, stork nest third village, Longhu Town, Chao'an District, Chaozhou City, Guangdong Province

Patentee before: Li Yanling