CN102070767A - Preparation method of anti-aging ultraviolet cured acrylic-polyurethane resin containing fluorine - Google Patents

Preparation method of anti-aging ultraviolet cured acrylic-polyurethane resin containing fluorine Download PDF

Info

Publication number
CN102070767A
CN102070767A CN 201010594310 CN201010594310A CN102070767A CN 102070767 A CN102070767 A CN 102070767A CN 201010594310 CN201010594310 CN 201010594310 CN 201010594310 A CN201010594310 A CN 201010594310A CN 102070767 A CN102070767 A CN 102070767A
Authority
CN
China
Prior art keywords
fluorine
preparation
ageing
urethane resin
ultraviolet light
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
CN 201010594310
Other languages
Chinese (zh)
Other versions
CN102070767B (en
Inventor
杜楠
梁红波
王力强
贾茹
谢春英
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.)
Chengdu Aircraft Industrial Group Co Ltd
Nanchang Hangkong University
Original Assignee
Chengdu Aircraft Industrial Group Co Ltd
Nanchang Hangkong University
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Chengdu Aircraft Industrial Group Co Ltd, Nanchang Hangkong University filed Critical Chengdu Aircraft Industrial Group Co Ltd
Priority to CN 201010594310 priority Critical patent/CN102070767B/en
Publication of CN102070767A publication Critical patent/CN102070767A/en
Application granted granted Critical
Publication of CN102070767B publication Critical patent/CN102070767B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Abstract

The invention provides a preparation method of anti-aging ultraviolet cured acrylic-polyurethane resin containing fluorine. The preparation method comprises the following steps: (1) adding polyisocyanate in a three-necked bottle; (2) after dropwise adding in the step (1), regulating the temperature of an oil bath pot, reacting for 4.5-8 hours, then stopping the reaction; (3) reacting for 8-12 hours at 50-70 DEG C; and (4) testing the product after the reaction in the step (3), determining the solid content of the product, and adding 5-15 parts of reactive monomer diluent by weight according to the solid content to obtain the product. The invention has the advantages that the preparation method is beneficial to spraying and construction; the curing time is shorter than that of the traditional UV-cured polyurethane, all the properties of the paint film are better, and the anti-aging property is improved.

Description

The preparation method of ageing-resistant ultraviolet light polymerization fluorine-containing urethane resin
Technical field
The present invention relates to a kind of preparation method of fluorine-containing urethane resin, relate in particular to a kind of preparation method of ageing-resistant ultraviolet light polymerization fluorine-containing urethane resin.
Background technology
Along with fast development of modern industry, more and more higher for the service requirements of coating, except basic water-fast, anti-solvent, oil resistant etc. require, in severe environment such as ultraviolet ray, ozone, acid rain, high low temperature alternation, also require to have certain erosion resistance.For the conduction of coating, grease proofing, waterproof, function such as heat insulation the part particular requirement is arranged also in addition.
Ultraviolet-curing paint has utilized ultraviolet radiation to make this curing new technology of paint solidification film forming, compares with thermofixation, and it has VOC free (volatile organic matter) release, saves the energy, production efficiency advantages of higher, is a kind of environmentally friendly technology.At present, UV-cured resin is widely used for fields such as chemical industry, electronics, light industry, machinery, transportation, communication with its unique technique advantage.But conventional UV-cured resin physical strength is relatively poor, and not ageing-resistant.
Urethane (PU) material can freely regulated soft or hard segment structure because of its uniqueness, the existing general application in elastomerics, fiber, coating and bonding agent field.Fluoro-containing group is introduced in the PU structure, the mechanical property and the two-phase microstructure features that had both kept the PU excellence, surface property and the overall performance of PU have been improved again to a great extent, give the material excellence low surface energy, refuse water, oil repellent, oilness, heat-resisting chemical-resistant and anti-staining property and excellent biological compatibility, become the emerging developing direction of PU at present.Because fluoroacrylate raw material monomer kind is many, synthetic relatively easy, so this fluorine introducing mode has bigger handiness and practical economic worth.For example, CN1882618A provides a kind of (methyl) acrylate that comprises the fluorinated alkyl and Photoepolymerizationinitiater initiater and can be as the fluorine-containing Photocurable composition of luminescent material etc., along with fluorine content increases, the hydrolytic resistance of filming, humidity resistance, surface property, optical characteristics, mechanical characteristic, stability in storage all have more excellent improvement.
Summary of the invention
The object of the present invention is to provide a kind of preparation method of ageing-resistant ultraviolet light polymerization fluorine-containing urethane resin, ultraviolet-curing paint exists moisture-proof heat, low temperature resistant, anti-mould, salt spray resistance, the relatively poor problem of oil resistance at present, the present invention is primarily aimed at above problem, adopt polyisocyanates, contain two key monohydroxy acrylate and poly-hydroxy fluorinated acrylate resin is a raw material, synthesized a kind of ageing-resistant UV by more manageable reaction conditions and method and solidified the fluorine-containing urethane resin.
The present invention is achieved like this, and it is characterized in that method steps is:
(1) there-necked flask, agitator, prolong, thermometer are installed, adjusting the oil bath pan temperature is 20 ~ 50 ℃, in there-necked flask, add 30 ~ 50 mass parts multicomponent isocyanates, at the uniform velocity drip 20 ~ 30 mass parts monohydroxy acrylate monomers and 0.1 ~ 1 mass parts of catalyst mixing solutions with constant pressure funnel in there-necked flask, rate of addition is controlled within 0.5 ~ 2 hour and drips off;
(2) after step (1) dropwises, adjusting the oil bath pan temperature is 50 ~ 70 ℃, heated and stirred reaction 4.5 ~ 8h under this temperature; With the Di-n-Butyl Amine that configures-acetone titration residual isocyanate group content, determine residual content, treat that it reaches stopped reaction behind the theoretical reacting value;
(3) in step (2) reaction product, add the fluorine-containing acrylic polyol resin of 15 ~ 30 mass parts, 0.1 ~ 1 mass parts of catalyst and 0.5 ~ 1.5 mass parts stopper, keep temperature of reaction at 50 ~ 70 ℃, reacted 8 ~ 12 hours, measure isocyanate group mass contg, stopped reaction after content is less than 2% with acetone-Di-n-Butyl Amine method;
(4) the reacted product of test procedure (3) is determined the solid content of product, adds the reactive monomer thinner of 5 ~ 15 weight parts according to solid content, promptly gets product.
Described fluorine-containing acrylic polyol resin is the fluorine-containing aliphatic acrylate of trifunctional, perfluoro alkyl phosphoester acrylic ester or fluorine-containing hyperbranched polyester acrylic ester.
Described multicomponent isocyanate is tolylene diisocyanate, isophorone diisocyanate, diphenylmethanediisocyanate, triphenylmethane triisocyanate, vulcabond low-grade polymer (trimerization/pentamer) and biuret, poly methylene poly phenyl poly isocyanate or hexamethylene diisocyanate trimer.
It is described that to contain two key monohydroxy acrylate be Hydroxyethyl acrylate, Propylene glycol monoacrylate, pentaerythritol diacrylate, tetramethylol methane tetraacrylate or TriMethylolPropane(TMP) mono alkenyl ether.
A kind of in the organo-metallic salt catalyzer such as tertiary amine catalysts such as described catalyzer is triethylamine, diethylene diamine, the N-methylmorpholine and two lauric acid butyl tin, stannous octoate and organo-bismuth.
Described stopper is branch subtype stoppers such as MEHQ, Resorcinol, para benzoquinone, phenothiazine, beta-phenyl naphthylamines, p-ten.-butylcatechol, perhaps a kind of in the inorganics such as cuprous chloride, iron trichloride.
Described polyhydroxy polycarboxylic acrylate resin is that the following material of solution polymerization makes: one or more (methyl) vinylformic acid and C1-C6 contain the esterification monomer of fluoroalkyl alcohol, and one or more (methyl) vinylformic acid and C1-C6 contain at least a kind of (methyl) acrylic ester monomer that contains hydroxyl of esterification monomer of fluoroalkyl alcohol.
Described reactive monomer thinner is Viscoat 295 (TMPTA), ethoxylated trimethylolpropane triacrylate (EO 3-TMPTA), propylene glycol diacrylate (DPGDA), tri (propylene glycol) diacrylate (TPGDA) or 1,6 hexanediol diacrylate (HDDA).
Advantage of the present invention is: selected multicomponent isocyanate and poly-hydroxy fluorinated acrylate itself are macromole and polyfunctional group, toxicity is little, the degree of crosslinking height, the every excellent performance of product of preparation and stable, the introducing of fluoropolymer can form thin film at substrate surface, substrate surface tension force is significantly reduced,, thereby show hydrophobic and oil repellent and anti-fouling functions less than general liquid.In addition, can regulate dope viscosity after the interpolation reactive thinner, help spraying application, set time while is faster than traditional UV curing urethane speed, and the every performance of paint film is more excellent, and has improved ageing resistance.
Embodiment
Embodiment 1:
Present embodiment illustrates the preparation method of ageing-resistant fluorine-containing urethane resin provided by the invention.
(1) adjusts oil bath pan temperature to 40 ℃, the diphenylmethanediisocyanate that in there-necked flask, adds 40 weight parts, utilize constant pressure funnel that the mixing solutions of the dibutyl tin laurate of 25 parts by weight of acrylic hydroxyl ethyl esters and 0.3 weight part is slowly splashed in the there-necked flask, dropwised in 2 hours;
(2) after step (1) dropwises, adjusting the oil bath pan temperature is 60 ℃, after 6 hours, measures isocyanate content every 1 hour with acetone-Di-n-Butyl Amine method in reaction under this temperature, after question response reaches preset value, i.e. and stopped reaction; The mixing solutions that reaction is obtained is poured into and is cooled to 30 ℃ in the constant pressure funnel
(3) the 4-oxygen sylvan of 30 weight part four-functional group fluorinated hydroxy acrylate, 0.3 part of catalyzer dibutyl tin laurate and 0.5 weight part is poured in the there-necked flask, mix the back and drip the reacted product of step (2), dropwise in 1 hour, reacted 10 hours down at 65 ℃, measure isocyanate group mass contg, stopped reaction after content is less than 2% with acetone-Di-n-Butyl Amine method;
(4) the reacted product of test procedure (3) is determined the solid content of product, adds the reactive monomer thinner of 15 weight parts according to solid content, promptly gets product.
Embodiment 2:
Present embodiment illustrates the preparation method of ageing-resistant fluorine-containing urethane resin provided by the invention.
(1) adjusts oil bath pan temperature to 40 ℃, the poly methylene poly phenyl poly isocyanate that in there-necked flask, adds 35 weight parts, utilize constant pressure funnel that the mixing solutions of the dibutyl tin laurate of the pentaerythritol diacrylate of 30 weight parts and 0.5 weight part is slowly splashed in the there-necked flask, dropwised in 1.5 hours;
(2) after step (1) dropwises, adjusting the oil bath pan temperature is 55 ℃, after 6 hours, measures isocyanate content every 1 hour with acetone-Di-n-Butyl Amine method in reaction under this temperature, after question response reaches preset value, i.e. and stopped reaction; The mixing solutions that reaction is obtained is poured into and is cooled to 30 ℃ in the constant pressure funnel
(3) dihydroxy-benzene of 25 weight part perfluoro alkyl phosphoester acrylic esters, 0.4 part of catalyzer dibutyl tin laurate and 0.5 weight part is poured in the there-necked flask, mix the back and drip the reacted product of step (2), dropwise in 1 hour, reacted 12 hours down at 60 ℃, measure isocyanate group mass contg, stopped reaction after content is less than 2% with acetone-Di-n-Butyl Amine method;
(4) the reacted product of test procedure (3) is determined the solid content of product, adds the reactive monomer thinner of 12 weight parts according to solid content, promptly gets product.
Embodiment 3:
Present embodiment illustrates the preparation method of ageing-resistant fluorine-containing urethane resin provided by the invention.
(1) adjusts oil bath pan temperature to 40 ℃, the poly methylene poly phenyl poly isocyanate that in there-necked flask, adds 35 weight parts, utilize constant pressure funnel that the mixing solutions of the dibutyl tin laurate of the pentaerythritol diacrylate of 30 weight parts and 0.5 weight part is slowly splashed in the there-necked flask, dropwised in 1.5 hours;
(2) after step (1) dropwises, adjusting the oil bath pan temperature is 55 ℃, after 6 hours, measures isocyanate content every 1 hour with acetone-Di-n-Butyl Amine method in reaction under this temperature, after question response reaches preset value, i.e. and stopped reaction; The mixing solutions that reaction is obtained is poured into and is cooled to 30 ℃ in the constant pressure funnel
(3) dihydroxy-benzene of the fluorine-containing hyperbranched polyester acrylic ester of 20 weight parts, 0.5 part of catalyzer dibutyl tin laurate and 0.6 weight part is poured in the there-necked flask, mix the back and drip the reacted product of step (2), dropwise in 1 hour, reacted 12 hours down at 60 ℃, measure isocyanate group mass contg, stopped reaction after content is less than 0.2% with acetone-Di-n-Butyl Amine method;
(4) the reacted product of test procedure (3) is determined the solid content of product, adds the reactive monomer thinner of 14 weight parts according to solid content, promptly gets product.
Embodiment 4:
The present embodiment explanation is that matrix resin prepares ageing-resistant fluorine-containing polyurethane resin coating with ageing-resistant fluorine-containing urethane resin provided by the invention.
Product among the embodiment 1 is taken out 100 weight parts, add 16.6 weight part titanium dioxides, 5.8 weight part talcum powder, 3.8 weight part light calcium carbonates, 3.2 weight part process whites, 5.4 weight part silicone oil, use the high speed shear dispersion machine, rotating speed is 3000 rev/mins, obtains ageing-resistant fluorine-containing urethane colored paint after 10 minutes.
Add 0.21 weight part light trigger TPO, 0.58 weight part light trigger 184, stir, leave standstill.
With the tinplate that 400 purpose sand paperings will apply, wipe clean with the base material that the wet cotton that speckles with alcohol will apply, according to GB 1727-1992 spraying paint film, film thickness is between 23-35 μ m.The panel that spraying is finished is placed on the ventilation, treats that solvent evaporates uses 600W ultraviolet light polymerization light irradiation after half an hour, and irradiation distance is 30cm, and irradiation time is no more than 50s.
Embodiment 5:
The present embodiment explanation is that matrix resin prepares ageing-resistant fluorine-containing polyurethane resin coating with ageing-resistant fluorine-containing urethane resin provided by the invention.
Product among the embodiment 2 is taken out 120 weight parts, add 23.5 weight part titanium dioxides, 1.6 weight part carbon blacks, 15 weight part talcum powder, 6.9 weight part light calcium carbonates, 9.8 weight part wilkinites, 4.5 weight part methyl-silicone oils, use the high speed shear dispersion machine, rotating speed is 3000 rev/mins, obtains ageing-resistant fluorine-containing urethane colored paint after 15 minutes.
Add 0.72 weight part light trigger, 819,0.31 weight part light triggers 1173, stir, leave standstill.
Adopt the base material that the same procedure processing will apply in the example 4, with quadrat method spraying paint film, curing.
Application Example 6:
The present embodiment explanation is that matrix resin prepares ageing-resistant fluorine-containing polyurethane resin coating with ageing-resistant fluorine-containing urethane resin provided by the invention.
Product among the embodiment 3 is taken out 150 weight parts, and the filler of equal in quality in adding and the Application Example 2 uses the high speed shear dispersion machine, and rotating speed is 3000 rev/mins, obtains ageing-resistant fluorine-containing urethane colored paint after 3 hours.
Add identical light trigger among the embodiment 5, stir, leave standstill.
Adopt the base material that the same procedure processing will apply among the embodiment 4, with quadrat method spraying paint film, curing.
Embodiment 7
Present embodiment illustrates the performance of ageing-resistant fluorine-containing polyurethane resin coating provided by the invention.
The resin that the foregoing description 4-6 is obtained carries out performance test, and it the results are shown in Table 1.
(1) solids coatings
Measure according to GB/T1725-1979 (1989);
(2) the drying varniss time
Test according to GB/T1728-1979 (1989);
(3) paint film thermotolerance
Test according to GB/T1733-1979 (1989).Heat-resisting back is placed 30min and is treated that it is cooled under the standard conditions naturally, detects impact property and sticking power in 1h;
(4) lower temperature resistance
Test plate (panel) with having prepared places-55 ± 2 ℃ refrigerator 4h, takes out test plate (panel), and 23 ± 2 ℃ of temperature, relative humidity is placed 30min 55 ± 5% times, checks paint film then;
(5) water tolerance
Carry out according to GB/T1733-1993, the water mark is dried with absorbent cotton or soft paper in water-fast back, places 30min and treats that it is cooled under the standard conditions naturally, detects pencil hardness and sticking power in 1h;
(6) humidity resistance
Carry out according to GB/T1740-1979 (1989), place 30min behind the humidity resistance and treat that it is cooled under the standard conditions naturally, detects sticking power in 1h;
(7) fungus resistance
Test according to GB/T1741-1979 (1989);
(8) salt fog resistance
Test according to GB/T1771-1991;
(9) anti-4109 lubricating oil
According among the GB/T9274-1988 5.4 carry out, dry oil stain with absorbent cotton or soft paper behind the oil resistant, place 30min and treat that it is cooled under the standard conditions naturally, detects pencil hardness, sticking power in 1h.
(10) anti-No. 3 rocket engine fuels
According among the GB/T9274-1988 5.4 carry out, dry oil stain with absorbent cotton or soft paper behind the oil resistant, place 30min and treat that it is cooled under the standard conditions naturally, detects pencil hardness, sticking power in 1h;
(11) anti-No. 10 hydraulic efficiency oil
According among the GB/T9274-1988 5.4 carry out, dry oil stain with absorbent cotton or soft paper behind the oil resistant, place 30min and treat that it is cooled under the standard conditions naturally, detects pencil hardness, sticking power in 1h;
(12) anti-No. 120 aviation spirit
According among the GB/T9274-1988 5.4 carry out, dry oil stain with absorbent cotton or soft paper behind the oil resistant, place 30min and treat that it is cooled under the standard conditions naturally, detects pencil hardness, sticking power in 1h.
Behind every anti-aging test, concrete data see the following form one to table three:
Table one
Figure 309979DEST_PATH_IMAGE001
Table two
Figure 820594DEST_PATH_IMAGE002
Table three
Figure 69173DEST_PATH_IMAGE003

Claims (8)

1. the preparation method of an ageing-resistant ultraviolet light polymerization fluorine-containing urethane resin is characterized in that method steps is:
(1) there-necked flask, agitator, prolong, thermometer are installed, adjusting the oil bath pan temperature is 20 ~ 50 ℃, in there-necked flask, add 30 ~ 50 mass parts multicomponent isocyanates, at the uniform velocity drip 20 ~ 30 mass parts monohydroxy acrylate monomers and 0.1 ~ 1 mass parts of catalyst mixing solutions with constant pressure funnel in there-necked flask, rate of addition is controlled within 0.5 ~ 2 hour and drips off;
(2) after step (1) dropwises, adjusting the oil bath pan temperature is 50 ~ 70 ℃, heated and stirred reaction 4.5 ~ 8h under this temperature; With the Di-n-Butyl Amine that configures-acetone titration residual isocyanate group content, determine residual content, treat that it reaches stopped reaction behind the theoretical reacting value;
(3) in step (2) reaction product, add the fluorine-containing acrylic polyol resin of 15 ~ 30 mass parts, 0.1 ~ 1 mass parts of catalyst and 0.5 ~ 1.5 mass parts stopper, keep temperature of reaction at 50 ~ 70 ℃, reacted 8 ~ 12 hours, measure isocyanate group mass contg, stopped reaction after content is less than 2% with acetone-Di-n-Butyl Amine method;
(4) the reacted product of test procedure (3) is determined the solid content of product, adds the reactive monomer thinner of 5 ~ 15 weight parts according to solid content, promptly gets product.
2. the preparation method of ageing-resistant ultraviolet light polymerization fluorine-containing urethane resin according to claim 1 is characterized in that described fluorine-containing acrylic polyol resin is the fluorine-containing aliphatic acrylate of trifunctional, perfluoro alkyl phosphoester acrylic ester or fluorine-containing hyperbranched polyester acrylic ester.
3. the preparation method of ageing-resistant ultraviolet light polymerization fluorine-containing urethane resin according to claim 1 is characterized in that described multicomponent isocyanate is tolylene diisocyanate, isophorone diisocyanate, diphenylmethanediisocyanate, triphenylmethane triisocyanate, vulcabond low-grade polymer (trimerization/pentamer) and biuret, poly methylene poly phenyl poly isocyanate or hexamethylene diisocyanate trimer.
4. the preparation method of ageing-resistant ultraviolet light polymerization fluorine-containing urethane resin according to claim 1 is characterized in that described to contain two key monohydroxy acrylate be Hydroxyethyl acrylate, Propylene glycol monoacrylate, pentaerythritol diacrylate, tetramethylol methane tetraacrylate or TriMethylolPropane(TMP) mono alkenyl ether.
5. the preparation method of ageing-resistant ultraviolet light polymerization fluorine-containing urethane resin according to claim 1, it is characterized in that a kind of in tertiary amine catalysts such as described catalyzer is triethylamine, diethylene diamine, the N-methylmorpholine and the organo-metallic salt catalyzer such as two lauric acid butyl tin, stannous octoate and organo-bismuth.
6. the preparation method of ageing-resistant ultraviolet light polymerization fluorine-containing urethane resin according to claim 1, it is characterized in that described stopper is branch subtype stoppers such as MEHQ, Resorcinol, para benzoquinone, phenothiazine, beta-phenyl naphthylamines, p-ten.-butylcatechol, perhaps a kind of in cuprous chloride, the iron trichloride inorganics.
7. the preparation method of ageing-resistant ultraviolet light polymerization fluorine-containing urethane resin according to claim 1, it is characterized in that described polyhydroxy polycarboxylic acrylate resin is that the following material of solution polymerization makes: one or more (methyl) vinylformic acid and C1-C6 contain the esterification monomer of fluoroalkyl alcohol, and one or more (methyl) vinylformic acid and C1-C6 contain at least a kind of (methyl) acrylic ester monomer that contains hydroxyl of esterification monomer of fluoroalkyl alcohol.
8. require the preparation method of described ageing-resistant ultraviolet light polymerization fluorine-containing urethane resin as right 6, be characterised in that described reactive monomer thinner is Viscoat 295 (TMPTA), ethoxylated trimethylolpropane triacrylate (EO 3-TMPTA), propylene glycol diacrylate (DPGDA), tri (propylene glycol) diacrylate (TPGDA) or 1,6 hexanediol diacrylate (HDDA).
CN 201010594310 2010-12-19 2010-12-19 Preparation method of anti-aging ultraviolet cured acrylic-polyurethane resin containing fluorine Expired - Fee Related CN102070767B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 201010594310 CN102070767B (en) 2010-12-19 2010-12-19 Preparation method of anti-aging ultraviolet cured acrylic-polyurethane resin containing fluorine

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 201010594310 CN102070767B (en) 2010-12-19 2010-12-19 Preparation method of anti-aging ultraviolet cured acrylic-polyurethane resin containing fluorine

Publications (2)

Publication Number Publication Date
CN102070767A true CN102070767A (en) 2011-05-25
CN102070767B CN102070767B (en) 2013-04-17

Family

ID=44029540

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 201010594310 Expired - Fee Related CN102070767B (en) 2010-12-19 2010-12-19 Preparation method of anti-aging ultraviolet cured acrylic-polyurethane resin containing fluorine

Country Status (1)

Country Link
CN (1) CN102070767B (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102659995A (en) * 2012-04-24 2012-09-12 南昌航空大学 Preparation method of ultraviolet-curable water-borne fluorinated paint with low surface energy
CN105837723A (en) * 2016-04-12 2016-08-10 湖南省金海科技有限公司 Ultraviolet light curing fluorocarbon resin and manufacturing method thereof
CN112608448A (en) * 2020-12-30 2021-04-06 江南大学 Preparation method of high-elasticity hand-feeling wear-resistant multi-arm photocuring resin

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006071567A1 (en) * 2004-12-28 2006-07-06 3M Innovative Properties Company Fluoroacrylate-multifunctional acrylate copolymer compositions
CN1882618A (en) * 2003-11-21 2006-12-20 大日本油墨化学工业株式会社 Fluorine containing photocurable composition
CN101020731A (en) * 2007-03-12 2007-08-22 安徽大学 Process of preparing solvent type fluoric acrylate copolymer

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1882618A (en) * 2003-11-21 2006-12-20 大日本油墨化学工业株式会社 Fluorine containing photocurable composition
WO2006071567A1 (en) * 2004-12-28 2006-07-06 3M Innovative Properties Company Fluoroacrylate-multifunctional acrylate copolymer compositions
CN101020731A (en) * 2007-03-12 2007-08-22 安徽大学 Process of preparing solvent type fluoric acrylate copolymer

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102659995A (en) * 2012-04-24 2012-09-12 南昌航空大学 Preparation method of ultraviolet-curable water-borne fluorinated paint with low surface energy
CN105837723A (en) * 2016-04-12 2016-08-10 湖南省金海科技有限公司 Ultraviolet light curing fluorocarbon resin and manufacturing method thereof
CN112608448A (en) * 2020-12-30 2021-04-06 江南大学 Preparation method of high-elasticity hand-feeling wear-resistant multi-arm photocuring resin

Also Published As

Publication number Publication date
CN102070767B (en) 2013-04-17

Similar Documents

Publication Publication Date Title
CN102050938B (en) Method for preparing ultraviolet photocuring polyurethane resin based on polybasic isocyanate and polybasic hydroxy polyacrylate
CN107254251B (en) A kind of aqueous UV urethane acrylate dispersoid and preparation method thereof with self-initiating function
CN107141867B (en) A kind of hard coat anti-fingerprint additive and preparation method thereof
CN108504269A (en) A kind of floride-free nonpolluting coating and preparation method thereof of ultraviolet light/sun light curable
CN105504215B (en) A kind of aqueous polyurethane emulsion of color inhibition and preparation method thereof
CN108456290A (en) A kind of dual cure polyurethane acrylate resin and preparation method thereof
CN102659995A (en) Preparation method of ultraviolet-curable water-borne fluorinated paint with low surface energy
CN105339408A (en) Polyisocyanate composition and method for production thereof, block polyisocyanate composition and method for production thereof, resin composition, curable resin composition, and cured article
CN105482680B (en) Ultraviolet light solidifies hyperbranched perfluoropolyether urethane acrylate paint
CN101967221B (en) Cleanable waterborne polyurethane coatings
CN108503847B (en) Fluorine-containing polyurethane/acrylate UV (ultraviolet) curing resin and preparation method thereof
CN107868598B (en) Coating composition
CN112574390A (en) High-wear-resistance UV resin with anti-fingerprint function and preparation method thereof
KR20080054588A (en) A method of manufacturing high adhesive polyurea coating agents and a method of coating high adhesive polyurea
CN105254843B (en) Polyisocyantates composition, blocked polyisocyanates composition and their manufacturing method
CN102070767B (en) Preparation method of anti-aging ultraviolet cured acrylic-polyurethane resin containing fluorine
CN101792619A (en) Fluorine-containing resin photocuring optical fiber coating composite and preparation method thereof
CN104968703B (en) The mutually non-isocyanate elastomer of segmentation
CN109575222A (en) A kind of composite modified UV of fluoro- sulphur solidifies the preparation method of multi-arm type aqueous polyurethane
CN111434740A (en) Ultraviolet-cured fluorine-containing polyurethane acrylate coating
JP6539106B2 (en) Polyisocyanate composition and method for producing the same, curable composition, cured product, and cured resin
CN103717632B (en) Photocurable resin composition and use its wet district component and functional panel
KR20170074204A (en) Acrylate-terminated urethane polybutadienes formed from low-monomer 1:1 monoadducts of reactive olefinic compounds and diisocyanates and hydroxy-terminated polybutadienes
CN113817126A (en) Reactive viscosity adjusting composition suitable for two-component water-based epoxy system and preparation method and application thereof
CN116023854B (en) High-hardness friction-resistant anti-fog coating and preparation method thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20130417

Termination date: 20131219