CN108587442A - A kind of ultraviolet optical coating and its preparation method with anti-mildew performance - Google Patents
A kind of ultraviolet optical coating and its preparation method with anti-mildew performance Download PDFInfo
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING 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
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
- C09D175/14—Polyurethanes having carbon-to-carbon unsaturated bonds
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
- C08G18/12—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step using two or more compounds having active hydrogen in the first polymerisation step
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- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
- C08G18/3802—Low-molecular-weight compounds having heteroatoms other than oxygen having halogens
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- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
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- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
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- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
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- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
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- C08G18/00—Polymeric products of isocyanates or isothiocyanates
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- C08G18/67—Unsaturated compounds having active hydrogen
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Abstract
The invention discloses a kind of ultraviolet optical coatings with anti-mildew performance, are prepared by the raw material including following parts by weight：The urethane acrylate of 80 100 parts by weight；The photoinitiator of 2.0 3.2 parts by weight；The organic silicon monomer containing unsaturated double-bond of 10 15 parts by weight；The reactive diluent of 30 50 parts by weight；The levelling agent of 0.33 1.5 parts by weight；The antifoaming agent of 0.33 1.5 parts by weight.The invention discloses a kind of ultraviolet optical coatings with anti-mildew performance, and anti-mildew performance is good, excellent transparency.Invention additionally discloses a kind of preparation methods of the ultraviolet optical coating with anti-mildew performance.
Description
Technical field
The invention belongs to chemical material technical fields, specifically, being related to a kind of ultraviolet light painting with anti-mildew performance
Material and its preparation method.
Background technology
Cooktop surface generally uses stainless steel plate, but stainless steel is of high cost, weight is big and is not easy cleaning-nursing, later
Large area replaces stainless steel plate using glass.Glass is a kind of relatively transparent non crystallized silicates nonmetallic materials,
The transparency and certain intensity, hardness, surface smoothness with light can compare favourably with mechanical polishing.Glass extensive use
In fields such as building, automobiles, have become a kind of basic means of production.Glass is the non-conductor of heat, and has fragility.When
When temperature difference inside and outside glass is too big, cause inside glass stress is inconsistent will cause glass since expansion rate is different
Cracking.Solve glass causes cracking glasses to be highly desirable due to uneven heating.Graphene is that known world is most thin, most hard
Hard nano material, single-layer graphene are almost fully transparent, only absorb 2.3% light, while the thermal coefficient of graphene is high
It is more taller than diamond up to 5300W/mK.
But prior art shortage is preferably applied graphene in burner glass surface to solve the equal heat problem of glass
Coating.
Ultraviolet-curing paint is a kind of new coating, in the coating photoinitiator after ultraviolet light, generate from
By base or ionic group, cause chemical anti-to cause the unsaturated double-bond of ultraviolet curable resin and active monomer diluent
It answers, realizes the solidification of coating.Compared with heat curing coating, ultraviolet-curing paint does not generate volatile organic matter in solidification process
Pollution, avoids in traditional coating solidification process and its serious exhaust emission, meanwhile, in ultraviolet-curing paint solidification process
Without heating, the energy expenditure of paint solidification process is saved, energy consumption is only the 1/5 of heat cure, the paint film layer tool of formation
There is the features such as wear-resisting, hardness is high, corrosion-resistant.This kind of coating is widely used to woodenware, plastic casing, fibre coating, doctor at present
The external coating in instrument and automobile industry is treated, market prospects are boundless.
Although ultraviolet-curing paint has above-mentioned many advantages, in many application fields, ultraviolet-curing paint
Film performance has a certain distance compared with traditional heat curing coating, wherein critically important one the reason is that ultraviolet light solidification apply
Material shrinking percentage in flash cure process is high, and it is poor to result in adhesive force.Especially PET sheet packaging material field, to table
The performance requirements such as finishing coat film hardness, the transparency and scratch-resistant are higher and higher, however, ultraviolet-curing paint is due to stronger
Convergent force results in adhesive force and is greatly reduced, and PET sheet brittleness is increased.Therefore, ultraviolet-curing paint is reduced
Shrinkage stress has a large amount of research and report.Chinese patent literature 201110189918.1 discloses a kind of alicyclic epoxy third
Olefin(e) acid ester prepolymer is to improve the shrinkage stress during paint solidification, but the prepolymer is by cycloaliphatic epoxy resin and propylene
Acid or methacrylic acid directly react, and the prepolymer molecular weight is smaller, and film is more crisp.Chinese patent literature
201410212211.1 disclosing a kind of alicyclic epoxy urethane acrylate ultraviolet-curing paint of modification, the coating
Chemical composition include modified alicyclic epoxy polyurethane acrylate prepolymer, active monomer diluent, photoinitiator, stream
Flat agent, adhesion promoter, the invention coating is small with curing system shrinking percentage, shock resistance is strong, cured film flexibility is good,
The features such as adhesive force is high.Above-mentioned this two patents reduce the contraction of paint film, improve adhesive force, so obtained from coating hardness
It is relatively low, it especially in PET sheet after application, will produce in use " mildew ".Chinese patent literature
201120306544.2 disclose a kind of UV coating structures of Wear-resistant scratch-resistant flower, including are applied in epoxy zinc rich primer layer, polyurethane
Layer and urethane acrylate top coat layer add abrasion-resistant powder in top coat layer, to improve the hardness and wearability of coating.It is Chinese special
Sharp document 201410075434.8 discloses a kind of safety and environmental protection wear-resistant ultraviolet ray solidified paint, by polyester acrylate, 1,6-
Hexanediyl ester, methoxy polyethylene glycol methacrylate-styrene polymer, photoinitiator, double pentaerythritol methacrylate, vinegar
Acid butyl ester, polymethylphenylsiloxane, antioxidant, nano-bentonite, nano bamboo carbon powder, IPBC and auxiliary agent are constituted.The invention
Nano-bentonite, nano bamboo carbon powder are added, good dispersion increases mobility, and nano bamboo carbon powder has good electromagnetism
Shielding action, and anion and far infrared can be discharged, it is safe to the human body harmless；Add auxiliary agent, good leveling property, film adhesive
Good, hardness is big, wear-resisting, energy conservation and environmental protection.This two patents are although improve the hardness and wearability of paint film, due to powder
Addition, reduce the light transmittance of paint film, cannot be satisfied coating for PET sheet and use.That is, up to the present,
Wear-resisting scratch-resistant ultraviolet-curing paint is prepared, the UV-cured resin of high functionality is typically used, and is added a small amount of
Abrasion-resistant powder, smooth powder or polyethylene wax improve scratch-resistant performance and wearability, however, with the addition of these fillers,
Result in the decline of the paint film transparency.If the PET sheet do not added filler, and can made generates a large amount of " mildew ", make its appearance
It is greatly reduced.
Thus, the ultraviolet-curing paint with anti-mildew function of high transparency has become PET sheet industry application
The very important coating of one kind.
Invention content
Based on this, it is necessary in view of the above-mentioned problems, a present invention wherein purpose is that open one kind having anti-mildew performance
Ultraviolet optical coating, there is anti-mildew performance, and excellent transparency.
To realize the above-mentioned technical purpose, specific technical solution is as follows：A kind of ultraviolet optical coating with anti-mildew performance,
It is characterized in that, is prepared by the raw material including following parts by weight：
The urethane acrylate of 80-100 parts by weight；
2.0-3.2 the photoinitiator of parts by weight；
The organic silicon monomer containing unsaturated double-bond of 10-15 parts by weight；
The reactive diluent of 30-50 parts by weight；
The levelling agent of 0.33-1.5 parts by weight；
The antifoaming agent of 0.33-1.5 parts by weight.
Preferably, the photoinitiator can be selected from IHT-PI907, Irgacure651, Irgacure184,
One kind in Irgacure369, Irgacure754, Irgacure2022, Irgacure 1173.
Preferably, the levelling agent can be selected from EFKA3883, EFKA3886, EFKA3600, BYK366,
It is a kind of in BYK333, BYK307, DEGO410.
Preferably, the antifoaming agent can be selected from EFKA2022, EFKA2527, EFKA2040, BYK352,
It is a kind of in BYK354, BYK357.
Preferably, the reactive diluent is 1,6- hexanediyl esters, tripropylene glycol diacrylate
Ester, trimethylolpropane trimethacrylate, ethoxyquin trimethylolpropane trimethacrylate, the third oxidation trimethylolpropane tris third
One kind in olefin(e) acid ester.
A kind of ultraviolet optical coating with anti-mildew performance disclosed by the invention has the beneficial effect that：With anti-mildew
Can, and excellent transparency.
The present invention also provides a kind of preparation methods of the ultraviolet optical coating with anti-mildew performance, include the following steps：
（1）Prepare urethane acrylate：
A. by the PolyTHF dihydric alcohol of 50-80 parts by weight, hydroxy-terminated polysiloxane dihydric alcohol, the 15-32 of 20-40 parts by weight
The 1H of parts by weight, 1H, 12 fluoro- 1,8- ethohexadiols of 8H, 8H- are at 100-120 DEG C, and decompression water removal 1-2 hours, then, nitrogen is protected
Under shield, 70-90 DEG C is cooled to, the polyisocyanates of 70-120 parts by weight and the osmanthus in December of 0.03-0.05 parts by weight is added
Sour dibutyl tin catalyst carries out reaction 1.5-3 hours, obtains the first intermediate；
B. under nitrogen protection by the first intermediate, temperature control is at 100-120 DEG C, be added 8-22 parts by weight containing double bond
Terminal hydroxy group acrylate monomer reacts 1-2.5 hours, obtains urethane acrylate；
（2）Urethane acrylate, the organic silicon monomer containing unsaturated double-bond, reactive diluent and antifoaming agent are added to sand milling
In machine, with the speed of 1000-1800rpm be sanded 1.5-3 hours；
（3）0.5-1.5 is sanded with the speed of 2500-3000rpm in middle addition photoinitiator and levelling agent in material after being sanded
Hour, it is filtered through filter screen, obtains the ultraviolet-curing paint of anti-mildew performance.
Preferably, the PolyTHF dihydric alcohol number-average molecular weight is preferably 1000-4000Da.
Preferably, the PolyTHF dihydric alcohol number-average molecular weight is preferably 1000-4000Da.
Preferably, the hydroxy-terminated polysiloxane dihydric alcohol is preferably 2000-5000Da.
Preferably, the polyisocyanates is IPDI tripolymers, TDI tripolymers.
Preferably, the organic silicon monomer containing unsaturated double-bond is vinyltrimethoxysilane, vinyl
One kind in triethoxysilane, acrylic trimethoxy silane and γ-methacryloxy front three oxosilane.
Preferably, the terminal hydroxy group acrylate monomer containing double bond is hydroxy-ethyl acrylate, metering system
Sour hydroxyl ethyl ester, pentaerythritol triacrylate or double pentaerythritol C5 methacrylate.
A kind of preparation method of ultraviolet optical coating with anti-mildew performance disclosed by the invention has the beneficial effect that：It prepares
Mould proof performance of ultraviolet optical coating with anti-mildew performance is good, and excellent transparency.
Specific implementation mode
Below with reference to specific embodiment, the present invention will be further described.
The synthesis of urethane acrylate, following examples 1-6.
Embodiment 1：Step 1：The terminal hydroxy group of the PolyTHF dihydric alcohol (molecular weight 1000Da) of 50g, 20g is poly-
The 1H of silicone glycols (molecular weight 1000Da), 15g, 1H, at 100 DEG C, decompression removes 12 fluoro- 1,8- ethohexadiols of 8H, 8H-
Then water 2 hours under nitrogen protection, cools to 70 DEG C, the IPDI tripolymers of 70g and the cinnamic acid two in December of 0.03g is added
Butyl tin catalyst carries out reaction 3 hours, obtains the first intermediate.
Step 2：Under nitrogen protection by the first intermediate, the pentaerythrite 3 third of 8g is added at 100 DEG C in temperature control
Olefin(e) acid ester reacts 2.5 hours, obtains product.
Embodiment 2：The synthesis of urethane acrylate,
Step 1：By the PolyTHF dihydric alcohol (molecular weight 1000Da) of 80g, the hydroxy-terminated polysiloxane dihydric alcohol of 40g
The 1H of (molecular weight 1000Da), 32g, 1H, 12 fluoro- 1,8- ethohexadiols of 8H, 8H- are at 120 DEG C, decompression water removal 1 hour, so
Afterwards, under nitrogen protection, 90 DEG C are cooled to, the December of TDI tripolymers and 0.05g that 120g is added is dilaurate catalysed
Agent carries out reaction 1.5 hours, obtains the first intermediate.
Step 2：Under nitrogen protection by the first intermediate, the acrylic acid hydroxyl second of 22g is added at 120 DEG C in temperature control
Ester reacts 1 hour, obtains product.
Embodiment 3：The synthesis of urethane acrylate,
Step 1：By the PolyTHF dihydric alcohol (molecular weight 4000Da) of 65g, the hydroxy-terminated polysiloxane dihydric alcohol of 30g
The 1H of (molecular weight 4000Da), 20g, 1H, 12 fluoro- 1,8- ethohexadiols of 8H, 8H- are at 110 DEG C, decompression water removal 1.5 hours, so
Afterwards, under nitrogen protection, 80 DEG C are cooled to, the dilaurylate in December of IPDI tripolymers and 0.04g that 100g is added is urged
Agent carries out reaction 2 hours, obtains the first intermediate.
Step 2：Under nitrogen protection by the first intermediate, the methacrylic acid of 10g is added at 110 DEG C in temperature control
Hydroxyl ethyl ester reacts 1.5 hours, obtains product.
Embodiment 4：The synthesis of urethane acrylate,
Step 1：By the PolyTHF dihydric alcohol (molecular weight 2000Da) of 70g, the hydroxy-terminated polysiloxane dihydric alcohol of 35g
The 1H of (molecular weight 2000Da), 25g, 1H, 12 fluoro- 1,8- ethohexadiols of 8H, 8H- are at 105 DEG C, decompression water removal 1 hour, so
Afterwards, under nitrogen protection, 85 DEG C are cooled to, the December of TDI tripolymers and 0.03g that 115g is added is dilaurate catalysed
Agent carries out reaction 2.5 hours, obtains the first intermediate.
Step 2：Under nitrogen protection by the first intermediate, the dipentaerythritol of 15g is added at 115 DEG C in temperature control
Five acrylate react 2 hours, obtain product.
Embodiment 5：The synthesis of urethane acrylate,
Step 1：By the PolyTHF dihydric alcohol (molecular weight 3000Da) of 75g, the hydroxy-terminated polysiloxane dihydric alcohol of 32g
The 1H of (molecular weight 3000Da), 28g, 1H, 12 fluoro- 1,8- ethohexadiols of 8H, 8H- are at 120 DEG C, decompression water removal 1 hour, so
Afterwards, under nitrogen protection, 80 DEG C are cooled to, the dilaurylate in December of IPDI tripolymers and 0.05g that 110g is added is urged
Agent carries out reaction 1.5 hours, obtains the first intermediate.
Step 2：Under nitrogen protection by the first intermediate, the pentaerythrite three of 20g is added at 110 DEG C in temperature control
Acrylate reacts 1-2.5 hours, obtains product.
Embodiment 6：The synthesis of urethane acrylate,
Step 1：By the PolyTHF dihydric alcohol (molecular weight 2500Da) of 65g, the hydroxy-terminated polysiloxane dihydric alcohol of 35g
The 1H of (molecular weight 2500Da), 18g, 1H, 12 fluoro- 1,8- ethohexadiols of 8H, 8H- are at 115 DEG C, decompression water removal 1.5 hours, so
Afterwards, under inert gas shielding, 75 DEG C are cooled to, the TDI tripolymers of 88g and the dilaurylate in December of 0.04g is added
Catalyst carries out reaction 2.5 hours, obtains the first intermediate.
Step 2：Under nitrogen protection by the first intermediate, the pentaerythrite five of 18g is added at 100 DEG C in temperature control
Acrylate reacts 1 hour, obtains product.
According to the material ratio of table 1, a kind of ultraviolet optical coating with anti-mildew performance is prepared in accordance with the following methods.Specifically
Preparation method is as follows：The first step, by the urethane acrylate of 80-100 parts by weight（What respectively Examples 1 to 6 was produced is poly-
Urethane acrylate）, the organic silicon monomer containing unsaturated double-bond of 10-15 parts by weight, the reactive diluent of 30-50 parts by weight and
The antifoaming agent of 0.33-1.5 parts by weight is added in sand mill, with the speed of 1000-1800rpm be sanded 1.5-3 hours.The
The levelling agent of the middle photoinitiator and 0.33-1.5 parts by weight that 2.0-3.2 parts by weight are added in two steps, the material after being sanded, with
The speed of 2500-3000rpm is sanded 0.5-1.5 hours, is filtered by the strainer of 100 mesh, obtains ultraviolet-curing paint.
It is respectively labeled as UVP1, UVP2, UVP3, UVP4, UVP5 and UVP6.
Table 1 prepares the material ratio of ultraviolet-curing paint：
Above-mentioned antifoaming agent EFKA2022 is Efka Products, and the EFKA2527 and EFKA2040 of Efka company also can be selected
Antifoaming agent, BYK354 and BYK357 are Bi Ke Products, and Bi Ke companies BYK352 antifoaming agent also can be selected.
Above-mentioned photoinitiator Irgacure184, Irgacure369 and Irgacure 1173 are BASF product, light-initiated
The other type products of BASF, such as Irgacure651, Irgacure754, Irgacure2022 also can be used in agent.
Above-mentioned levelling agent EFKA3883 be Efka Products, also can be selected for Efka Products EFKA3886,
EFKA3600 levelling agents, levelling agent BYK333 are Bi Ke Products, and BYK366, BYK307 levelling of Bi Ke companies also can be selected
Agent, levelling agent TEG0410 are the high Products of enlightening.
UVP1, UVP2, UVP3, UVP4, UVP5 and UVP6 are coated on the PET polyester films of 0.2-0.5mm respectively, with
The UV energy of 170-300mJ/cm2 carries out photocuring, obtains 1.5-3 microns of paint films.
The paint film is tested for the property, test result is shown in Table 2, and table 2 is provided in an embodiment of the present invention transparent mould proof
The ultraviolet-curing paint of point obtains the performance test results of film.
The ultraviolet-curing paint of 2 anti-mildew of table obtains the performance test results such as following table of film：
Several embodiments of the present invention above described embodiment only expresses, the description thereof is more specific and detailed, but can not be because
This and be construed as limiting the scope of the patent.It should be pointed out that for those of ordinary skill in the art, not
Under the premise of being detached from present inventive concept, various modifications and improvements can be made, these are all within the scope of protection of the present invention.Cause
This, the protection domain of patent of the present invention should be determined by the appended claims.
Claims (11)
1. a kind of ultraviolet optical coating with anti-mildew performance, which is characterized in that it is prepared by the raw material including following parts by weight
It forms：
The urethane acrylate of 80-100 parts by weight；
2.0-3.2 the photoinitiator of parts by weight；
The organic silicon monomer containing unsaturated double-bond of 10-15 parts by weight；
The reactive diluent of 30-50 parts by weight；
The levelling agent of 0.33-1.5 parts by weight；
The antifoaming agent of 0.33-1.5 parts by weight.
2. a kind of ultraviolet optical coating with anti-mildew performance as described in claim 1, which is characterized in that the photoinitiator
For Irgacure651, Irgacure184, Irgacure369, Irgacure754, Irgacure2022, Irgacure 1173
One or more of.
3. a kind of ultraviolet optical coating with anti-mildew performance as described in claim 1, which is characterized in that the levelling agent is
It is one or more of in EFKA3883, EFKA3886, EFKA3600, BYK366, BYK333, BYK307, DEGO410.
4. a kind of ultraviolet optical coating with anti-mildew performance as described in claim 1, which is characterized in that the antifoaming agent is
It is one or more of in EFKA2022, EFKA2527, EFKA2040, BYK352, BYK354, BYK357.
5. a kind of ultraviolet optical coating with anti-mildew performance as described in claim 1, which is characterized in that the activity dilution
Agent is 1,6 hexanediol diacrylate, tripropylene glycol diacrylate, trimethylolpropane trimethacrylate, ethoxyquin three
One kind in hydroxymethyl-propane triacrylate, the third oxidation trimethylolpropane trimethacrylate.
6. a kind of preparation method of the ultraviolet optical coating with anti-mildew performance, which is characterized in that include the following steps：
（1）Prepare urethane acrylate：
A. by the PolyTHF dihydric alcohol of 50-80 parts by weight, hydroxy-terminated polysiloxane dihydric alcohol, the 15-32 of 20-40 parts by weight
The 1H of parts by weight, 1H, 12 fluoro- 1,8- ethohexadiols of 8H, 8H- are at 100-120 DEG C, and decompression water removal 1-2 hours, then, nitrogen is protected
Under shield, 70-90 DEG C is cooled to, the polyisocyanates of 70-120 parts by weight and the osmanthus in December of 0.03-0.05 parts by weight is added
Sour dibutyl tin catalyst carries out reaction 1.5-3 hours, obtains the first intermediate；
B. under nitrogen protection by the first intermediate, temperature control is at 100-120 DEG C, be added 8-22 parts by weight containing double bond
Terminal hydroxy group acrylate monomer reacts 1-2.5 hours, obtains urethane acrylate；
（2）Urethane acrylate, the organic silicon monomer containing unsaturated double-bond, reactive diluent and antifoaming agent are added to sand milling
In machine, with the speed of 1000-1800rpm be sanded 1.5-3 hours；
（3）Photoinitiator and levelling agent are added in material after being sanded, it is small that 0.5-1.5 is sanded with the speed of 2500-3000rpm
When, it is filtered through filter screen, obtains the ultraviolet-curing paint of anti-mildew performance.
7. a kind of preparation method of the ultraviolet optical coating with anti-mildew performance as claimed in claim 6, which is characterized in that described poly-
Tetrahydrofuran dihydric alcohol molecular weight is 1000-4000Da.
8. a kind of preparation method of the ultraviolet optical coating with anti-mildew performance as claimed in claim 6, which is characterized in that the end
Hydroxyl polysiloxane dihydric alcohol molecular weight is 2000-5000Da.
9. a kind of preparation method of the ultraviolet optical coating with anti-mildew performance as claimed in claim 6, which is characterized in that described more
Isocyanates is IPDI tripolymers or TDI tripolymers.
10. a kind of preparation method of the ultraviolet optical coating with anti-mildew performance as claimed in claim 6, which is characterized in that described
Organic silicon monomer containing unsaturated double-bond is vinyltrimethoxysilane, vinyltriethoxysilane, acrylic trimethoxy
One kind in base silane and γ-methacryloxy front three oxosilane.
11. a kind of preparation method of the ultraviolet optical coating with anti-mildew performance as claimed in claim 6, which is characterized in that described
Terminal hydroxy group acrylate monomer containing double bond is hydroxy-ethyl acrylate, hydroxyethyl methacrylate, three acrylic acid of pentaerythrite
Ester or double pentaerythritol C5 methacrylate.
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Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007117907A1 (en) * | 2006-03-30 | 2007-10-18 | Basf Corporation | Coatings for polycarbonate windows |
| CN102060974A (en) * | 2010-12-21 | 2011-05-18 | 东莞市贝特利新材料有限公司 | Synthesis method of organosilicon-modified aqueous polyurethane acrylate |
| CN103642382A (en) * | 2013-11-25 | 2014-03-19 | 中国科学院长春应用化学研究所 | Ultraviolet light curing anti-fouling paint and preparation method thereof |
| CN105482766A (en) * | 2015-12-31 | 2016-04-13 | 广西科技大学 | Polyurethane acrylate UV-curing material and preparation method thereof |
-
2018
- 2018-03-28 CN CN201810264369.1A patent/CN108587442A/en active Pending
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007117907A1 (en) * | 2006-03-30 | 2007-10-18 | Basf Corporation | Coatings for polycarbonate windows |
| CN102060974A (en) * | 2010-12-21 | 2011-05-18 | 东莞市贝特利新材料有限公司 | Synthesis method of organosilicon-modified aqueous polyurethane acrylate |
| CN103642382A (en) * | 2013-11-25 | 2014-03-19 | 中国科学院长春应用化学研究所 | Ultraviolet light curing anti-fouling paint and preparation method thereof |
| CN105482766A (en) * | 2015-12-31 | 2016-04-13 | 广西科技大学 | Polyurethane acrylate UV-curing material and preparation method thereof |
Non-Patent Citations (1)
| Title |
|---|
| 盛茂桂等: "《新型聚氨酯树脂涂料生产技术与应用》", 28 February 2001, 广东科技出版社 * |
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