CN108300336A - A kind of UV visbreakings composition, UV visbreaking films and preparation method thereof - Google Patents

A kind of UV visbreakings composition, UV visbreaking films and preparation method thereof Download PDF

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Publication number
CN108300336A
CN108300336A CN201810105706.2A CN201810105706A CN108300336A CN 108300336 A CN108300336 A CN 108300336A CN 201810105706 A CN201810105706 A CN 201810105706A CN 108300336 A CN108300336 A CN 108300336A
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China
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visbreakings
byk
antistatic
agent
ester
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闫勇
陈伟
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Suzhou City-State Dali Material Technology Co Ltd
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Suzhou City-State Dali Material Technology Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J4/00Adhesives based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; adhesives, based on monomers of macromolecular compounds of groups C09J183/00 - C09J183/16
    • C09J4/06Organic 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 C09J159/00 - C09J187/00
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J9/00Adhesives characterised by their physical nature or the effects produced, e.g. glue sticks
    • C09J9/02Electrically-conducting adhesives
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2203/00Applications of adhesives in processes or use of adhesives in the form of films or foils
    • C09J2203/326Applications of adhesives in processes or use of adhesives in the form of films or foils for bonding electronic components such as wafers, chips or semiconductors
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2301/00Additional features of adhesives in the form of films or foils
    • C09J2301/10Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet
    • C09J2301/12Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers
    • C09J2301/122Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers the adhesive layer being present only on one side of the carrier, e.g. single-sided adhesive tape
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2301/00Additional features of adhesives in the form of films or foils
    • C09J2301/30Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier
    • C09J2301/312Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier parameters being the characterizing feature
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2423/00Presence of polyolefin
    • C09J2423/006Presence of polyolefin in the substrate
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2427/00Presence of halogenated polymer
    • C09J2427/006Presence of halogenated polymer in the substrate
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2467/00Presence of polyester
    • C09J2467/005Presence of polyester in the release coating
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2467/00Presence of polyester
    • C09J2467/006Presence of polyester in the substrate

Abstract

The present invention relates to protection technical field of membrane, more particularly, to a kind of UV visbreakings composition, UV dehesion films and preparation method thereof.The UV visbreakings composition is mainly made of the following raw material by weight percentage:High temperature resistant acrylate pressure-sensitive adhesive resin 20% 50%, polyfunctionality oligomer and/or polyfunctional monomer 1% 30%, crosslinking agent 0.3% 2%, antistatic agent 0.1% 5%, dispersant 0 2%, levelling agent 0.2% 2%, photoinitiator 0.5% 5% and solvent 25% 60%.The UV visbreakings film includes substrate layer and coating UV anti-adhesive layers thereon and release film layer.There is the UV visbreakings composition excellent bonding force, UV pre-irradiations to have high adhesion, and peeling force is high, has low adhesion power after UV irradiations, peeling force is low, and antistatic effect is good, and can be resistant to 120 DEG C of high temperature 30min not residue glues.

Description

A kind of UV visbreakings composition, UV visbreaking films and preparation method thereof
Technical field
The present invention relates to protection technical field of membrane, more particularly, to a kind of UV visbreakings composition, UV dehesions film and its preparation Method.
Background technology
In semiconductor process, when carrying out semiconductor crystal wafer cutting, polishing, to reduce silicon thin layer defect concentration, often It is often used wafer cutting visbreaking protective film.Visbreaking protective film refers to that bonding force is strong when in use, and in later stage stripping process, it glues Resultant force weakens to remove.
Visbreaking protective film currently on the market is mostly UV visbreaking protective films, refers to having high adhesion power in UV pre-irradiations, Adhesion is good, and bonding force is decreased obviously after UV irradiations, is easily peeled off.Cut for wafer on domestic market and pick technique etc. The UV visbreakings glue of protection is mostly based on Japan, TaiWan, China, and domestic UV visbreakings glue is also several to be promoted in research and development, but performance is not yet Complete stability.Also, the base material of UV visbreaking protective films in use due to rubbing action be easy to generate electrostatic, for The use in the more demanding electronic component field of electrostatic is restricted, for example is easy absorption dust, is then transferred into the production of fitting Product surface or electrostatic potential are excessively high, cause part to generate bad etc..In addition, current visbreaking protective film is after applied at elevated temperature, Residue glue is be easy to cause to be not easy to remove.
In view of this, special propose the present invention.
Invention content
The first object of the present invention is to provide a kind of UV visbreakings composition have excellent peeling force in UV pre-irradiations, Peeling force, which declines to a great extent, after UV irradiations is easily peeled off, and has excellent anti-static electrification, and can be resistant to 120 DEG C of high temperature 30 minutes not residue glues.
The second object of the present invention is to provide a kind of UV visbreakings film, and the UV visbreakings film has excellent in UV pre-irradiations Peeling force, peeling force, which declines to a great extent, after UV irradiations is easily peeled off, and has excellent anti-static electrification, can be resistant to 120 DEG C The not residue glue of high temperature 30 minutes.
Another object of the present invention is to provide a kind of preparation method of the UV visbreakings film, the preparation method operative employees Skill is simple, favorable repeatability.
In order to realize that the above-mentioned purpose of the present invention, spy use following technical scheme:
A kind of UV visbreakings composition, is mainly made of the following raw material by weight percentage:
High temperature resistant acrylate pressure-sensitive adhesive resin 20%-50%, polyfunctionality oligomer and/or polyfunctional monomer 1%- 30%, crosslinking agent 0.3%-2%, antistatic agent 0.1%-5%, dispersant 0-2%, levelling agent 0.2%-2%, photoinitiator 0.5%-5% and solvent 25%-60%.
Wherein, the high temperature resistant acrylic pressure sensitive gum resin cohesive force is high, is resistant to 120 DEG C of hot conditions, and 30min not residue glues, so as to improve the residue glue situation of the UV visbreakings composition.
Preferably, the high temperature resistant acrylate pressure-sensitive adhesive resin is solvent-type acrylic ester pressure-sensitive adhesive.More preferably , the molecular weight of the high temperature resistant acrylate pressure-sensitive adhesive resin is 100,000-200 ten thousand.It is further preferred that the solvent type third The solid content of olefin(e) acid ester pressure-sensitive adhesive is 20%-60%, viscosity 200cps-20000cps.
The UV visbreaking compositions that the present invention is prepared by above-mentioned raw materials have excellent bonding force, UV pre-irradiations tool There is high adhesion, peeling force is high, has low adhesion power after UV irradiations, UV peeling forces are low, and antistatic effect is good, can be resistant to 120 DEG C High temperature not residue glue.The polyfunctionality oligomer and/or polyfunctional monomer itself generate cross-linking reaction, crosslinking after UV irradiates Larger volume contraction is generated after reaction makes to generate fold between the UV visbreakings composition and adherend body surface face, and fold is big Position generates micropore, and contact area between UV visbreakings composition and adherend body surface face is made to reduce, to realize that visbreaking acts on.
Acrylate pressure-sensitive adhesive resin, under smaller active force, you can firm bonding force is formed, without other Means can be closely bonded with adherend.Conventional acrylic ester pressure-sensitive resin, though have many advantages, such as that initial bonding strength is big, due to Its architectural characteristic, heat resistance is poor, easily softens under high temperature and loses cementability, and hot conditions use appearance after substrate surface fitting It is also easy to produce residue glue.And the present invention uses high temperature resistant acrylate pressure-sensitive adhesive resin, under the premise of ensureing stripping performance, improves UV The high temperature resistance of visbreaking composition uses not residue glue under hot conditions.
Preferably, the antistatic agent includes organic antistatic agents, inorganic filler type antistatic agent and compound antistatic It is one or more in agent.Preferred antistatic agent is GW-2008 antistatic agents, GW-2006 antistatic agents and GW-3000C It is one or more in antistatic agent.Foregoing antistatic agents are Hui Gaojinbiao Science and Technology Ltd.s of Shenzhen.
Preferably, the inorganic filler type antistatic agent includes nano graphite powder, nano-graphene, carbon nanotube and nanometer It is one or more in silver wire.
Preferably, the grain size of the nano graphite powder is 50-100nm.
Preferably, the nano-graphene grain size is 5-20nm.
Preferably, the nano-silver thread line footpath is 20-80nm.
Preferably, a diameter of 5-30nm that the carbon nanotube is, length are 1-30 μm.
Preferably, the polyfunctionality oligomer includes aliphatic urethane acrylate oligomer and epoxy acrylate One or both of oligomer.
Preferably, the polyfunctional monomer includes pentaerythritol tetraacrylate, double pentaerythritol C5 methacrylate, two Six acrylate of pentaerythrite, trimethylolpropane trimethacrylate, dipentaerythritol hexaacrylate, trimethylolpropane tris Acrylate, ethoxyquin trimethylolpropane trimethacrylate, trimethylol-propane trimethacrylate, methacrylic acid- 2- hydroxy methacrylates, acrylamide, dimethacrylate -1,6-HD ester, diacrylate -1,6-HD ester, diacrylate Glycol ester, diacrylate triethyleneglycol ester, diacrylate tripropylene glycol ester, diacrylate are to neopentyl glycol ester, trihydroxy methyl third Alkane triacrylate, trihydroxy methyl pentane trimethyl acrylic ester, trimethylolpropane pentaerythritol triacrylate, the third oxidation In neopentylglycol diacrylate, ethoxyquin 1,6 hexanediol diacrylate and three (2- acrylyl oxy-ethyls) isocyanuric acid esters It is one or more.
Preferably, the crosslinking agent includes one in isocyanates crosslinking agent, amine cross-linking agent, aziridines crosslinking agent Kind is a variety of, preferably isocyanates crosslinking agent.
Preferably, the isocyanates crosslinking agent include isophorone diisocyanate, hexamethylene diisocyanate, One in dicyclohexyl methyl hydride diisocyanate, benzene dimethylene diisocyanate and tetramethylxylylene diisocyanate Kind is a variety of.It is furthermore preferred that the crosslinking agent is hexamethylene diisocyanate, preferably N3390 (Beyer Co., Ltd) crosslinking agent.
Preferably, the amine cross-linking agent includes in diethylenetriamines, trien and hexamethylenetetramine It is one or more.
Preferably, the dispersant includes 1104 and of BYK-170, BYK-164, BYK-180, BYK-182, Lencolo It is one or more in Lencolo1105.Described BYK-170, BYK-164, BYK-180, BYK-182 are Bi Ke companies of Germany , the Lencolo 1104 and Lencolo 1105 are that Dongguan City three paints industrial chemicals Co., Ltd.
Preferably, the levelling agent includes Lencolo 3001, Lencolo 3003, BYK-333, BYK-306, BYK- 390, one or more in BYK-354 and BYK-380.The Lencolo 3001, Lencolo 3003 paint for Dongguan City three Industrial chemicals Co., Ltd, described BYK-333, BYK-306, BYK-390, BYK-354 and BYK-380 are Germany Bi Ke public Department.
Preferably, the photoinitiator includes 2- isopropyl thioxanthones (ITX), 1- hydroxycyclohexyl phenyl ketones (184), 2- hydroxy-methyls phenyl third, benzoin dimethylether (651), benzophenone (BP), 2- methyl-1s-(4- methylthio phenyls Base) -2- morpholinyl -1- acetone (907), 2,4,6- (trimethylbenzoyl)-diphenyl phosphine oxide (TPO), alkane -1- ketone (1173), one or more in DR-575, preferably 2,4,6- (trimethylbenzoyl)-diphenyl phosphine oxides (TPO).
Preferably, the solvent include acetone, cyclohexanone, ethyl acetate, butyl acetate, butanone, methanol, ethyl alcohol, propyl alcohol, Isopropanol, isobutanol, n-butanol, methylisobutylketone, isophorone, toluene, dimethylbenzene, propylene glycol monomethyl ether, dipropylene glycol methyl ether In one or more, preferably butanone.
The method of the UV visbreakings composition is not unique, above-mentioned raw materials can be mixed evenly in proportion and subtract to get UV Tacking compositions.It is preferred that mixing time is 1-5h, more preferably 2h.
The present invention also provides a kind of UV visbreakings films, including substrate layer, UV anti-adhesive layers and the release film layer being bonded successively, In, the UV anti-adhesive layers are to be coated on base material layer surface by the UV visbreakings composition, and drying curing obtains.
Preferably, surface resistivity≤10 of the substrate layer11Ω/□.It is furthermore preferred that the substrate layer includes antistatic Any one of PET film, antistatic PO films, antistatic PVC film.It is further preferred that the thickness of the substrate layer is 50-150 μm, preferably 75-125 μm, more preferably 100 μm.
Preferably, the thickness of the UV anti-adhesive layers is 10-30 μm, preferably 15-25 μm, more preferably 20 μm.
Preferably, the release film layer is PET release film layers.It is furthermore preferred that the off-type force of the release film layer is 10- 100gf.It is further preferred that the thickness of the release film layer is 20-50 μm.
The present invention also provides a kind of preparation methods of the UV visbreakings film, include the following steps:
UV visbreaking compositions are coated on base material layer surface, release film layer is bonded on UV visbreaking compositions after preliminary drying, it is ripe Change, obtains the UV visbreakings film.
Preferably, 1-5mi n are dried under the conditions of the preliminary drying is included in 100 ± 10 DEG C, are preferably dried under the conditions of 100 DEG C 2mi n。
Preferably, the cooking conditions are to cure 20-30h under the conditions of 60 ± 10 DEG C, are preferably cured for 24 hours at 60 DEG C.
Compared with prior art, beneficial effects of the present invention are:
(1) UV visbreaking compositions of the invention have excellent bonding force in UV pre-irradiations, up to 1580gf, are shone in UV It penetrates rear bonding force and declines to a great extent and be easily peeled off, and there is excellent anti-static electrification, and it is not residual to can be resistant to 120 DEG C of high temperature Glue;
(2) the UV visbreakings film that UV visbreakings composition using the present invention obtains has excellent bonding force in UV pre-irradiations, Bonding force, which declines to a great extent, after UV irradiations is easily peeled off, and has excellent anti-static electrification, and can be resistant to 120 DEG C of high temperature Not residue glue;
(3) the preparation method operating procedure of UV visbreakings film of the present invention is simple, and production efficiency is high, favorable repeatability.
Description of the drawings
It, below will be to specific in order to illustrate more clearly of the specific embodiment of the invention or technical solution in the prior art Embodiment or attached drawing needed to be used in the description of the prior art are briefly described, it should be apparent that, in being described below Attached drawing is some embodiments of the present invention, for those of ordinary skill in the art, before not making the creative labor It puts, other drawings may also be obtained based on these drawings.
Fig. 1 is a kind of UV visbreaking membrane structure diagrams of specific implementation mode of the present invention.
Reference numeral:
1- substrate layers;2-UV anti-adhesive layers;3- release film layers.
Specific implementation mode
Technical scheme of the present invention is clearly and completely described below in conjunction with the drawings and specific embodiments, but Be it will be understood to those of skill in the art that it is following described embodiments are some of the embodiments of the present invention, rather than it is whole Embodiment is merely to illustrate the present invention, and is not construed as limiting the scope of the invention.Based on the embodiments of the present invention, ability The every other embodiment that domain those of ordinary skill is obtained without making creative work, belongs to guarantor of the present invention The range of shield.The person that is not specified actual conditions in embodiment, carries out according to conventional conditions or manufacturer's recommended conditions.Agents useful for same Or production firm person is not specified in instrument, is the conventional products that can be obtained by commercially available purchase.
In the description of the present invention, it should be noted that term "center", "upper", "lower", "left", "right", "vertical", The orientation or positional relationship of the instructions such as "horizontal", "inner", "outside" be based on the orientation or positional relationship shown in the drawings, merely to Convenient for the description present invention and simplify description, do not indicate or imply the indicated device or element must have a particular orientation, With specific azimuth configuration and operation, therefore it is not considered as limiting the invention.In addition, term " first ", " second ", " third " is used for description purposes only, and is not understood to indicate or imply relative importance.
UV visbreakings composition of the present invention, is mainly made of the following raw material by weight percentage:
High temperature resistant acrylate pressure-sensitive adhesive resin 20%-50%, polyfunctionality oligomer and/or polyfunctional monomer 1%- 30%, crosslinking agent 0.3%-2%, antistatic agent 0.1%-5%, dispersant 0-2%, levelling agent 0.2%-2%, photoinitiator 0.5%-5% and solvent 25%-60%.
In a kind of preferred embodiment of the present invention, the high temperature resistant acrylate pressure-sensitive adhesive resin is solvent type third Olefin(e) acid ester pressure-sensitive adhesive.It is furthermore preferred that the molecular weight of the high temperature resistant acrylate pressure-sensitive adhesive resin is 100,000-200 ten thousand.Into One step is preferred, and the solid content of the solvent-type acrylic ester pressure-sensitive adhesive is 20%-60%, viscosity 200cps- 20000cps。
Using specific high temperature resistant acrylate pressure-sensitive adhesive resin, the bonding of the UV visbreakings composition is helped to improve Power improves peeling force, and improves the high temperature resistance of the UV visbreakings composition, makes it under the high temperature conditions using not occurring The case where residue glue.
In a kind of preferred embodiment of the present invention, the polyfunctionality oligomer includes aliphatic polyurethane propylene One or both of acid esters oligomer and epoxy acrylate oligomer;The polyfunctional monomer includes pentaerythrite 4 third Olefin(e) acid ester, double pentaerythritol C5 methacrylate, dipentaerythritol hexaacrylate, trimethylolpropane trimethacrylate, two seasons Penta tetrol, six acrylate, trimethylolpropane trimethacrylate, ethoxyquin trimethylolpropane trimethacrylate, trihydroxy methyl Propane trimethyl acrylic ester, methacrylic acid -2- hydroxy methacrylates, acrylamide, dimethacrylate -1,6-HD ester, Diacrylate -1,6-HD ester, ethylene glycol diacrylate, diacrylate triethyleneglycol ester, diacrylate tripropylene glycol ester, two Acrylic acid is to neopentyl glycol ester, trimethylolpropane trimethacrylate, trihydroxy methyl pentane trimethyl acrylic ester, trihydroxy methyl Propane pentaerythritol triacrylate, third oxidation neopentylglycol diacrylate, ethoxyquin 1,6 hexanediol diacrylate and It is one or more in three (2- acrylyl oxy-ethyls) isocyanuric acid esters.
Using specific polyfunctionality oligomer and/or polyfunctional monomer, during polymerizing curable, crosslinking is improved Degree increases bonding force, to improve the peeling resistance before the UV processing of UV visbreaking compositions.
In a kind of preferred embodiment of the present invention, the crosslinking agent includes isocyanates crosslinking agent, amine friendship Join agent, one or more in aziridines crosslinking agent, preferably isocyanates crosslinking agent.
In a kind of preferred embodiment of the present invention, the isocyanates crosslinking agent includes two isocyanide of isophorone Acid esters, hexamethylene diisocyanate, dicyclohexyl methyl hydride diisocyanate, benzene dimethylene diisocyanate and durol It is one or more in dimethylene diisocyanate.It is furthermore preferred that the crosslinking agent is hexamethylene diisocyanate, preferably For N3390 (Beyer Co., Ltd) crosslinking agent.The amine cross-linking agent includes diethylenetriamines, trien and six methines It is one or more in tetramine.
Using specific crosslinking agent, the crosslinking curing between each raw material is peomoted, fully improves gained UV visbreakings combination The bonding force of object, peeling resistance.
In a kind of preferred embodiment of the present invention, the antistatic agent includes organic antistatic agents, inorganic filler It is one or more in type antistatic agent and composite antistatic agent, it is preferred that the antistatic agent includes GW-2008 antistatic It is one or more in agent, GW-2006 antistatic agents and GW-3000C antistatic agents.Foregoing antistatic agents are Shenzhen's remittance Gao Jin Mark Science and Technology Ltd..The inorganic filler type antistatic agent includes nano graphite powder, nano-graphene, carbon nanotube and receives It is one or more in rice silver wire.The grain size of the nano graphite powder is preferably 50-100nm;The nano-graphene grain size is excellent It is selected as 5-20nm;The nano-silver thread line footpath is preferably 20-80nm.
Using specific antistatic agent, contribute to the sheet resistance for reducing the UV visbreakings composition, improve antistatic property, Can meet the needs of practical application.
In a kind of preferred embodiment of the present invention, the dispersant includes BYK-170, BYK-164, BYK- 180, one or more in BYK-182, Lencolo 1104 and Lencolo 1105.Described BYK-170, BYK-164, BYK- 180, BYK-182 is Bi Ke companies of Germany, and the Lencolo1104 and Lencolo1105 are that Dongguan City three paints industrial chemicals Co., Ltd.
Using specific dispersant, the mutually dispersion peomoted between each raw material is miscible, keeps stock dispersion uniform, fills Divide the bonding force and antistatic property for improving the UV visbreakings composition.
In a kind of preferred embodiment of the present invention, the levelling agent include Lencolo3001, It is one or more in Lencolo3003, BYK-333, BYK-306, BYK-390, BYK-354 and BYK-380.It is described Lencolo 3001, Lencolo 3003 are that Dongguan City three paints industrial chemicals Co., Ltd, the BYK-333, BYK-306, BYK-390, BYK-354 and BYK-380 are Bi Ke companies of Germany.
In a kind of preferred embodiment of the present invention, the photoinitiator includes 2- isopropyl thioxanthones (I TX), 1- hydroxycyclohexyl phenyl ketones (184), 2- hydroxy-methyls phenyl third, benzoin dimethylether (651), benzophenone (BP), 2- methyl-1s-(4- methyl mercaptos phenyl) -2- morpholinyl -1- acetone (907), 2,4,6- (trimethylbenzoyl)-two It is one or more in phenyl phosphine oxide (TPO), alkane -1- ketone (1173), DR-575, preferably 2,4,6- (trimethylbenzoyls Base)-diphenyl phosphine oxide (TPO).
In a kind of preferred embodiment of the present invention, the solvent includes acetone, cyclohexanone, ethyl acetate, acetic acid Butyl ester, butanone, methanol, ethyl alcohol, propyl alcohol, isopropanol, isobutanol, n-butanol, methylisobutylketone, isophorone, toluene, diformazan It is one or more in benzene, propylene glycol monomethyl ether, dipropylene glycol methyl ether, preferably butanone.
Fig. 1 is a kind of UV visbreaking membrane structure diagrams of specific implementation mode of the present invention, and the UV visbreakings film includes successively Substrate layer 1, UV anti-adhesive layers 2 and the release film layer 3 of fitting.Wherein, the UV anti-adhesive layers are to be coated on base by UV visbreaking compositions Material layer surface, drying curing obtain.
In a kind of preferred embodiment of the present invention, surface resistivity≤10 of the substrate layer11Ω /□.It is described Substrate layer is provided simultaneously with antistatic property with UV anti-adhesive layers, further enhances the antistatic property of the UV visbreakings film.It is more excellent Choosing, the substrate layer includes any one of antistatic PET film, antistatic PO films, antistatic PVC film.The base The thickness of material layer is 50-150 μm, preferably 75-125 μm, more preferably 100 μm.
In a kind of preferred embodiment of the present invention, the thickness of the UV anti-adhesive layers is 10-30 μm, preferably 15- 25 μm, more preferably 20 μm.
In a kind of preferred embodiment of the present invention, the release film layer is PET release film layers, and preferred thickness is 20-50 μm, preferred off-type force is 10-100gf.
Embodiment 1
UV visbreaking compositions described in the present embodiment, raw material composition are as follows:
40g high temperature resistant acrylic pressure sensitive gum resins (production firm:Changxing Chemical Industry (china) Co., Ltd., model: ETERAC7710), 20g polyfunctionalities oligomer (production firm:Chemical drug chemical industry (Wuxi) Co., Ltd, model:UX- 5805W), 1g crosslinking agents (production firm:Bayer A.G, model:N3390), 3g antistatic agents (production firm:Shenzhen Hui Gaojinbiao Science and Technology Ltd.s, model:GW-2008), 0.8g dispersants (production firm:German Bi Ke companies, model: BYK-170), 0.2g levelling agents (production firm:German Bi Ke companies, model:BYK-333), 2,4,6- (trimethylbenzenes of 5g Formoxyl)-diphenyl phosphine oxide (TPO), 30g butanone.
Wherein, the UX-5805W is aliphatic urethane acrylate oligomer.
Embodiment 2
UV visbreaking compositions described in the present embodiment, raw material composition are as follows:
40g high temperature resistant acrylic pressure sensitive gum resins (production firm:Changxing Chemical Industry (china) Co., Ltd., model: ETERAC7710), 20g polyfunctionalities oligomer (production firm:Chemical drug chemical industry (Wuxi) Co., Ltd, model:UX- 5805W), 1g crosslinking agents (production firm:Bayer A.G, model:N3390), 2g nano graphite powders (production firm:Shanghai You Mo composite materials Co., Ltd), 0.8g dispersants (production firm:German Bi Ke companies, model:BYK-164), 0.2g flows Flat agent (production firm:German Bi Ke companies, model:BYK-306), 2,4,6- (trimethylbenzoyl)-dipheny oxide of 5g Change the butanone of phosphine (TPO), 31g.
Wherein, the particle size range of the nano graphite powder is 50-100nm.
Embodiment 3
UV visbreaking compositions described in the present embodiment, raw material composition are as follows:
40g high temperature resistant acrylic pressure sensitive gum resins (production firm:Changxing Chemical Industry (china) Co., Ltd., model: ETERAC7710), 20g polyfunctionalities oligomer (production firm:Chemical drug chemical industry (Wuxi) Co., Ltd, model:UX- 5805W), 1g crosslinking agents (production firm:Bayer A.G, model:N3390), 0.2g nano-graphenes (production firm:It closes Fertile micro crystal material Science and Technology Ltd.), 0.8g dispersants (production firm:German Bi Ke companies, model:BYK-180)、0.2g Levelling agent (production firm:German Bi Ke companies, model:BYK-390), 2,4,6- (trimethylbenzoyl)-diphenyl of 5g The butanone of phosphine oxide (TPO), 32.8g.
Wherein, the particle size range of the nano-graphene is 5-20nm.
Embodiment 4
UV visbreaking compositions described in the present embodiment, raw material composition are as follows:
40g high temperature resistant acrylic pressure sensitive gum resins (production firm:Changxing Chemical Industry (china) Co., Ltd., model: ETERAC7710), 20g polyfunctionalities oligomer (production firm:Chemical drug chemical industry (Wuxi) Co., Ltd, model:UX- 5805W), 1g crosslinking agents (production firm:Bayer A.G, model:N3390), 0.2g nano-silver threads (production firm:Hefei Micro crystal material Science and Technology Ltd.), 0.8g dispersants (production firm:German Bi Ke companies, model:BYK-182), 0.2g flows Flat agent (production firm:German Bi Ke companies, model:BYK-354), 2,4,6- (trimethylbenzoyl)-dipheny oxide of 5g Change the butanone of phosphine (TPO), 32.8g.
Wherein, the wire range of the nano-silver thread is 20-80nm.
Embodiment 5
UV visbreaking compositions described in the present embodiment, raw material composition are as follows:
40g high temperature resistant acrylic pressure sensitive gum resins (production firm:Changxing Chemical Industry (china) Co., Ltd., model: ETERAC7710), 20g polyfunctionalities oligomer (production firm:Chemical drug chemical industry (Wuxi) Co., Ltd, model:UX- 5805W), 1g crosslinking agents (production firm:Bayer A.G, model:N3390), 0.2g carbon nanotubes (production firm:Hefei Micro crystal material Science and Technology Ltd., model:CF-0), 0.8g dispersants (production firm:German Bi Ke companies, model:BYK- 182), 0.2g levelling agents (production firm:German Bi Ke companies, model:BYK-380), 2,4,6- (trimethylbenzoyls of 5g Base)-diphenyl phosphine oxide (TPO), 32.8g butanone.
Wherein, a diameter of 5-30nm of the carbon nanotube, length are 1-30 μm.
Embodiment 6
UV visbreaking compositions described in the present embodiment, raw material composition are as follows:
50g high temperature resistant acrylic pressure sensitive gum resins (production firm:Changxing Chemical Industry (china) Co., Ltd., model: ETERAC7710), 5g polyfunctionalities oligomer (production firm:Chemical drug chemical industry (Wuxi) Co., Ltd, model:UX-5805W)、 0.3g crosslinking agents (production firm:Bayer A.G, model:N3390), 5g antistatic agents (production firm:Converge Gao Jin for Shenzhen Mark Science and Technology Ltd., model:GW-2008), 2g dispersants (production firm:Dongguan City three paints industrial chemicals Co., Ltd, type Number:Lencolo 1104), 2g levelling agents (production firm:Dongguan City three paints industrial chemicals Co., Ltd, model:Lencolo 3001), the isopropanol of the 2- isopropyl thioxanthones (ITX) of 0.5g, 35.2g.
Embodiment 7
UV visbreaking compositions described in the present embodiment, raw material composition are as follows:
20g high temperature resistant acrylic pressure sensitive gum resins (production firm:Changxing Chemical Industry (china) Co., Ltd., model: ETERAC7710), 30g pentaerythritol tetraacrylates, 2g crosslinking agents (production firm:Bayer A.G, model:N3390)、 1g nano graphite powders (production firm:Shanghai You Mo composite materials Co., Ltd), 1g dispersants (production firm:Dongguan City three paints Industrial chemicals Co., Ltd, model:Lencolo1105), 1g levelling agents (production firm:Dongguan City three paints the limited public affairs of industrial chemicals Department, model:Lencolo3003), the toluene of the 1- hydroxycyclohexyl phenyl ketones (184) of 5g, 40g.
Embodiment 8
UV visbreaking compositions described in the present embodiment, raw material composition are as follows:
20g high temperature resistant acrylic pressure sensitive gum resins (production firm:Changxing Chemical Industry (china) Co., Ltd., model: ETERAC7710), 15g polyfunctionalities oligomer (production firm:Chemical drug chemical industry (Wuxi) Co., Ltd, model:UX- 5805W), 1g crosslinking agents (production firm:Bayer A.G, model:N3390), 1g nano graphite powders (production firm:Shanghai You Mo composite materials Co., Ltd), 2g levelling agents (production firm:Dongguan City three paints industrial chemicals Co., Ltd, model: Lencolo 3003), the propylene glycol monomethyl ether of the 2- hydroxy-methyls phenyl third of 1g, 60g.
Embodiment 9
The preparation method of UV visbreaking compositions described in embodiment 1-8, includes the following steps:
Each component is put in proportion into reaction kettle, 1-5h is stirred, preferably stirs 2h to get to the UV visbreakings group Close object.
The present embodiment additionally provides a kind of UV visbreakings that the UV visbreaking compositions using described in embodiment 1-8 are prepared Film, the UV visbreakings film are included in the substrate layer being bonded successively, UV anti-adhesive layers and release film layer, and the UV anti-adhesive layers are by institute It states UV visbreaking compositions and is coated on the formation of base material layer surface, the release film layer fits in UV anti-adhesive layers;Wherein, the UV subtracts Adhesion coating is to be coated on base material layer surface by the UV visbreakings composition, and drying curing obtains.The sheet resistance of the substrate layer Rate≤1011Ω/□.The substrate layer includes any in antistatic PET film, antistatic PO films, antistatic PVC films Kind.The thickness of the substrate layer is 50-150 μm, preferably 100 μm.The thickness of the UV anti-adhesive layers is 10-30 μm, preferably 20μm。
Specifically, the preparation method of the UV visbreakings film includes the following steps:
The UV visbreaking compositions that embodiment 1-8 is obtained are respectively coated the antistatic PET films (factory in 100 μ m-thicks Quotient:Toray, model:XY53 on), it is placed in preliminary drying 2min in 100 DEG C of baking ovens, release film is bonded on UV visbreaking compositions surface It is put into 60 DEG C of baking ovens and cures for 24 hours, obtain the UV visbreakings film.Wherein, the painting of UV visbreaking compositions is adjusted according to actual demand Cover thickness, in the present embodiment, thickness is 20 μm after keeping UV visbreaking compositions dry.
Experimental example 1
For the performance of the UV visbreaking compositions of each embodiment of comparative illustration, method described in embodiment 9 will be used with reality Apply UV visbreakings film (number is 1,2,3,4,5,6,7 and 8 respectively) progressive that the UV visbreaking compositions described in a 1-8 are prepared It can test, test result is shown in Table 1.
Wherein, the test method of the high temperature resistance is to fit in the UV visbreakings film on steel plate, in 120 DEG C of items Under part after 5mi n, UV irradiations, UV irradiation intensities are 230mW/cm2, irradiation time is 5-10s (being 8s when test), to steel Plate surface residue glue situation is detected.
The performance test results for the UV visbreaking films that 1 difference UV visbreaking compositions of table are prepared
As seen from the above table, UV visbreakings composition of the invention has excellent bonding force in UV pre-irradiations, up to 1580gf, Bonding force, which declines to a great extent, after UV irradiations is easily peeled off, and has excellent anti-static electrification, and under high temperature environment after use, Residue glue will not be caused in adhesive substrates.
Finally it should be noted that:The above embodiments are only used to illustrate the technical solution of the present invention., rather than its limitations;To the greatest extent Present invention has been described in detail with reference to the aforementioned embodiments for pipe, it will be understood by those of ordinary skill in the art that:Its according to So can with technical scheme described in the above embodiments is modified, either to which part or all technical features into Row equivalent replacement;And these modifications or replacements, various embodiments of the present invention technology that it does not separate the essence of the corresponding technical solution The range of scheme.

Claims (10)

1. a kind of UV visbreakings composition, which is characterized in that be mainly made of the following raw material by weight percentage:
High temperature resistant acrylate pressure-sensitive adhesive resin 20%-50%, polyfunctionality oligomer and/or polyfunctional monomer 1%- 30%, crosslinking agent 0.3%-2%, antistatic agent 0.1%-5%, dispersant 0-2%, levelling agent 0.2%-2%, photoinitiator 0.5%-5% and solvent 25%-60%.
2. UV visbreakings composition according to claim 1, which is characterized in that the high temperature resistant acrylate pressure-sensitive adhesive resin For solvent-type acrylic ester pressure-sensitive adhesive;
Preferably, the molecular weight of the high temperature resistant acrylate pressure-sensitive adhesive resin is 100,000-200 ten thousand;
Preferably, the solid content of the solvent-type acrylic ester pressure-sensitive adhesive is 20%-60%, viscosity 200cps- 20000cps。
3. UV visbreakings composition according to claim 1 or 2, which is characterized in that the antistatic agent includes organic anti-quiet It is one or more in electric agent, inorganic filler type antistatic agent and composite antistatic agent;
Preferably, the inorganic filler type antistatic agent includes nano graphite powder, nano-graphene, carbon nanotube and nano-silver thread In it is one or more;
It is furthermore preferred that the grain size of the nano graphite powder is 50-100nm;
It is furthermore preferred that the nano-graphene grain size is 5-20nm;
It is furthermore preferred that the nano-silver thread line footpath is 20-80nm;
It is furthermore preferred that a diameter of 5-30nm of the carbon nanotube, length is 1-30 μm.
4. UV visbreakings composition according to claim 1 or 2, which is characterized in that the polyfunctionality oligomer includes fat One or both of fat race urethane acrylate oligomer and epoxy acrylate oligomer;
Preferably, the polyfunctional monomer includes pentaerythritol tetraacrylate, double pentaerythritol C5 methacrylate, two seasons penta Six acrylate of tetrol, trimethylolpropane trimethacrylate, dipentaerythritol hexaacrylate, trimethylolpropane tris propylene Acid esters, ethoxyquin trimethylolpropane trimethacrylate, trimethylol-propane trimethacrylate, methacrylic acid -2- hydroxyls Base ethyl ester, acrylamide, dimethacrylate -1,6-HD ester, diacrylate -1,6-HD ester, diacrylate second two Alcohol ester, diacrylate triethyleneglycol ester, diacrylate tripropylene glycol ester, diacrylate are to neopentyl glycol ester, trimethylolpropane tris Acrylate, trihydroxy methyl pentane trimethyl acrylic ester, trimethylolpropane pentaerythritol triacrylate, the third oxidation new penta One in omega-diol diacrylate, ethoxyquin 1,6 hexanediol diacrylate and three (2- acrylyl oxy-ethyls) isocyanuric acid esters Kind is a variety of.
5. UV visbreakings composition according to claim 1 or 2, which is characterized in that the crosslinking agent includes isocyanates It is one or more in crosslinking agent, amine cross-linking agent, aziridines crosslinking agent;
Preferably, the crosslinking agent is isocyanates crosslinking agent;
Preferably, the isocyanates crosslinking agent includes isophorone diisocyanate, hexamethylene diisocyanate, two rings One kind in hexyl methane diisocyanate, benzene dimethylene diisocyanate and tetramethylxylylene diisocyanate or It is a variety of;
It is furthermore preferred that the crosslinking agent is hexamethylene diisocyanate.
6. UV visbreakings composition according to claim 1 or 2, which is characterized in that the photoinitiator includes 2- isopropyls Thioxanthone, 1- hydroxycyclohexyl phenyl ketones, 2- hydroxy-methyls phenyl third, benzoin dimethylether, benzophenone, 2- methyl- 1- (4- methyl mercaptos phenyl) -2- morpholinyl -1- acetone, 2,4,6- (trimethylbenzoyl)-diphenyl phosphine oxide, alkane -1- ketone, It is one or more in DR-575;
Preferably, the photoinitiator is 2,4,6- (trimethylbenzoyl)-diphenyl phosphine oxides.
7. UV visbreakings composition according to claim 1 or 2, which is characterized in that the dispersant include BYK-170, It is one or more in BYK-164, BYK-180, BYK-182, Lenco l o 1104 and Lenco l o1105;
Preferably, the levelling agent includes Lenco l o 3001, Lenco l o 3003, BYK-333, BYK-306, BYK- 390, one or more in BYK-354 and BYK-380;
Preferably, the solvent includes acetone, cyclohexanone, ethyl acetate, butyl acetate, butanone, methanol, ethyl alcohol, propyl alcohol, isopropyl In alcohol, isobutanol, n-butanol, methylisobutylketone, isophorone, toluene, dimethylbenzene, propylene glycol monomethyl ether, dipropylene glycol methyl ether It is one or more;
It is furthermore preferred that the solvent is butanone.
8. a kind of UV visbreakings film, which is characterized in that including substrate layer, UV anti-adhesive layers and the release film layer being bonded successively;
Wherein, the UV anti-adhesive layers are to be coated on base material layer surface by any one of the claim 1-7 UV visbreakings compositions, are dried What dry curing obtained.
9. UV visbreakings film according to claim 8, which is characterized in that surface resistivity≤10 of the substrate layer11Ω/ □;
Preferably, the substrate layer includes any one of antistatic PET film, antistatic PO films, antistatic PVC film;
Preferably, the thickness of the substrate layer is 50-150 μm;
Preferably, the thickness of the UV anti-adhesive layers is 10-30 μm.
10. the preparation method of the UV visbreaking films described in claim 8 or 9, which is characterized in that include the following steps:
UV visbreaking compositions are coated on base material layer surface, release film layer is bonded on UV visbreaking compositions after preliminary drying, cures, obtains To the UV visbreakings film;
Preferably, 1-5mi n are dried under the conditions of the preliminary drying is included in 100 ± 10 DEG C;
It is furthermore preferred that the preliminary drying is to dry 2mi n under the conditions of 100 DEG C;
Preferably, the cooking conditions are to cure 20-30h under the conditions of 60 ± 10 DEG C;
It is furthermore preferred that the cooking conditions are to be cured for 24 hours at 60 DEG C.
CN201810105706.2A 2018-02-02 2018-02-02 A kind of UV visbreakings composition, UV visbreaking films and preparation method thereof Pending CN108300336A (en)

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Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108864975A (en) * 2018-07-27 2018-11-23 威士达半导体科技(张家港)有限公司 A kind of Degumming method
CN110256983A (en) * 2019-06-21 2019-09-20 广东硕成科技有限公司 A kind of UV visbreaking protective film and preparation method thereof
CN110408351A (en) * 2019-06-28 2019-11-05 昆山博益鑫成高分子材料有限公司 A kind of UV visbreaking adhesive resistant to high temperature and protection membrane preparation method
CN110437760A (en) * 2019-09-23 2019-11-12 上海精珅新材料有限公司 The stable process film production method of processing procedure and products thereof of adhesion strength after a kind of high temperature
CN110484150A (en) * 2019-08-28 2019-11-22 昆山博益鑫成高分子材料有限公司 A kind of high temperature resistant UV visbreaking adhesive tape
CN110791222A (en) * 2019-12-02 2020-02-14 苏州泰仑电子材料有限公司 Environment-friendly emulsion type ultra-low peeling force protective film
CN111057474A (en) * 2019-12-24 2020-04-24 合肥乐凯科技产业有限公司 Adhesive for UV (ultraviolet) anti-adhesive film and UV anti-adhesive film thereof
CN111171741A (en) * 2020-02-14 2020-05-19 安徽富印新材料有限公司 High-temperature-resistant UV (ultraviolet) peelable pressure-sensitive adhesive film and preparation method thereof
CN112300431A (en) * 2020-11-08 2021-02-02 合肥乐凯科技产业有限公司 Optical diffusion film
CN113583595A (en) * 2021-09-16 2021-11-02 常州驰科光电科技有限公司 Thermal-viscosity-reducing adhesive, thermal-viscosity-reducing automatic-stripping protective film and preparation method
CN113773780A (en) * 2021-09-06 2021-12-10 张宁 Antistatic UV (ultraviolet) viscosity-reducing adhesive suitable for mass transfer and preparation method thereof
CN115232578A (en) * 2022-08-17 2022-10-25 苏州赛伍应用技术股份有限公司 UV viscosity-reducing adhesive and preparation method thereof
CN115477911A (en) * 2022-10-13 2022-12-16 南通市力盟新材料科技有限公司 Acid and alkali resistant UV viscosity-reducing composition and preparation process thereof

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1727426A (en) * 2004-07-26 2006-02-01 日东电工株式会社 Adhesive composition, adhesive sheets, and surface protecting film
JP2006045475A (en) * 2004-08-09 2006-02-16 Nitto Denko Corp Pressure-sensitive adhesive composition, pressure-sensitive adhesive sheet and the like, and surface protection film
CN101175830A (en) * 2005-05-20 2008-05-07 日东电工株式会社 Adhesive composition, adhesive sheet, and surface protection film
CN101243153A (en) * 2005-09-05 2008-08-13 日东电工株式会社 Adhesive composition, adhesive sheet and surface-protecting film
CN101243152A (en) * 2005-09-05 2008-08-13 日东电工株式会社 Adhesive composition, adhesive sheet, and surface-protective film
CN105778806A (en) * 2016-03-18 2016-07-20 张家港康得新光电材料有限公司 Heat-resistant UV visbreaking glue composition and UV visbreaking protective film
CN106995665A (en) * 2017-04-11 2017-08-01 新纶科技(常州)有限公司 A kind of heat resistant type UV visbreaking films and preparation method thereof
CN107022319A (en) * 2017-04-01 2017-08-08 东莞市睿泰涂布科技有限公司 The preparation technology of antistatic UV visbreakings composition, diaphragm and the diaphragm
CN206635285U (en) * 2017-03-28 2017-11-14 上海精涂新材料技术有限公司 Antistatic supporter diaphragm

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1727426A (en) * 2004-07-26 2006-02-01 日东电工株式会社 Adhesive composition, adhesive sheets, and surface protecting film
JP2006045475A (en) * 2004-08-09 2006-02-16 Nitto Denko Corp Pressure-sensitive adhesive composition, pressure-sensitive adhesive sheet and the like, and surface protection film
CN101175830A (en) * 2005-05-20 2008-05-07 日东电工株式会社 Adhesive composition, adhesive sheet, and surface protection film
CN101243153A (en) * 2005-09-05 2008-08-13 日东电工株式会社 Adhesive composition, adhesive sheet and surface-protecting film
CN101243152A (en) * 2005-09-05 2008-08-13 日东电工株式会社 Adhesive composition, adhesive sheet, and surface-protective film
CN105778806A (en) * 2016-03-18 2016-07-20 张家港康得新光电材料有限公司 Heat-resistant UV visbreaking glue composition and UV visbreaking protective film
CN206635285U (en) * 2017-03-28 2017-11-14 上海精涂新材料技术有限公司 Antistatic supporter diaphragm
CN107022319A (en) * 2017-04-01 2017-08-08 东莞市睿泰涂布科技有限公司 The preparation technology of antistatic UV visbreakings composition, diaphragm and the diaphragm
CN106995665A (en) * 2017-04-11 2017-08-01 新纶科技(常州)有限公司 A kind of heat resistant type UV visbreaking films and preparation method thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
杨鸣波: "《塑料成型工艺学》", 30 June 2014, 中国轻工出版社 *

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108864975A (en) * 2018-07-27 2018-11-23 威士达半导体科技(张家港)有限公司 A kind of Degumming method
CN108864975B (en) * 2018-07-27 2020-11-10 威士达半导体科技(张家港)有限公司 Degumming method
CN110256983A (en) * 2019-06-21 2019-09-20 广东硕成科技有限公司 A kind of UV visbreaking protective film and preparation method thereof
CN110408351A (en) * 2019-06-28 2019-11-05 昆山博益鑫成高分子材料有限公司 A kind of UV visbreaking adhesive resistant to high temperature and protection membrane preparation method
CN110484150A (en) * 2019-08-28 2019-11-22 昆山博益鑫成高分子材料有限公司 A kind of high temperature resistant UV visbreaking adhesive tape
CN110437760A (en) * 2019-09-23 2019-11-12 上海精珅新材料有限公司 The stable process film production method of processing procedure and products thereof of adhesion strength after a kind of high temperature
CN110791222A (en) * 2019-12-02 2020-02-14 苏州泰仑电子材料有限公司 Environment-friendly emulsion type ultra-low peeling force protective film
CN111057474A (en) * 2019-12-24 2020-04-24 合肥乐凯科技产业有限公司 Adhesive for UV (ultraviolet) anti-adhesive film and UV anti-adhesive film thereof
CN111171741A (en) * 2020-02-14 2020-05-19 安徽富印新材料有限公司 High-temperature-resistant UV (ultraviolet) peelable pressure-sensitive adhesive film and preparation method thereof
CN112300431A (en) * 2020-11-08 2021-02-02 合肥乐凯科技产业有限公司 Optical diffusion film
CN112300431B (en) * 2020-11-08 2022-04-15 合肥乐凯科技产业有限公司 Optical diffusion film
CN113773780A (en) * 2021-09-06 2021-12-10 张宁 Antistatic UV (ultraviolet) viscosity-reducing adhesive suitable for mass transfer and preparation method thereof
CN113583595A (en) * 2021-09-16 2021-11-02 常州驰科光电科技有限公司 Thermal-viscosity-reducing adhesive, thermal-viscosity-reducing automatic-stripping protective film and preparation method
CN115232578A (en) * 2022-08-17 2022-10-25 苏州赛伍应用技术股份有限公司 UV viscosity-reducing adhesive and preparation method thereof
CN115232578B (en) * 2022-08-17 2024-02-23 苏州赛伍应用技术股份有限公司 UV (ultraviolet) adhesive and preparation method thereof
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