CN106978112A - It is explosion-proof in a kind of mobile phone to use OCA optical cements - Google Patents
It is explosion-proof in a kind of mobile phone to use OCA optical cements Download PDFInfo
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- CN106978112A CN106978112A CN201710281396.5A CN201710281396A CN106978112A CN 106978112 A CN106978112 A CN 106978112A CN 201710281396 A CN201710281396 A CN 201710281396A CN 106978112 A CN106978112 A CN 106978112A
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- Prior art keywords
- reactor
- mobile phone
- explosion
- proof
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Classifications
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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
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J151/00—Adhesives based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers
- C09J151/003—Adhesives based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers grafted on to macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F265/00—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00
- C08F265/04—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00 on to polymers of esters
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
- C08F220/1808—C8-(meth)acrylate, e.g. isooctyl (meth)acrylate or 2-ethylhexyl (meth)acrylate
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2451/00—Presence of graft polymer
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2467/00—Presence of polyester
- C09J2467/005—Presence of polyester in the release coating
Abstract
The present invention provide it is explosion-proof in a kind of mobile phone use OCA optical cements, by the material of following mass percentage content it is reacted after be made:Acrylic polymer 50~80%;Isobornyl methacrylate 5~40%, ethyl acrylate 10~25%, initiator 0.1~5%;Acrylic polymer by the material of following weight/mass percentage composition it is reacted after be made:Isooctyl acrylate monomer 20~60%, methyl methacrylate 10~35%, the ethylhexyl 10~35% of methacrylic acid 2, hydroxy-ethyl acrylate 3~8%, molecular weight regulator 3~8%, azo dibutyronitrile 0.1~2%, the molecular weight regulator is the one or more in n-dodecyl mercaptan, tert-dodecylmercaotan, the different monooctyl ester of tri-thiol propionic acid.The beneficial effects of the present invention are explosion-proof in mobile phone to use OCA optical cements, service life is long, and weatherability, yellowing resistance are good, and environmental protection effect is good, excellent performance, moderate.
Description
Technical field
It is explosion-proof in particularly a kind of mobile phone to use OCA optical cements the present invention relates to a kind of OCA optical cements.
Background technology
In addition to handset capability, cell phone appearance also becomes the big key element that people choose mobile phone, in wanting for this key element
Ask down, cell phone rear cover becomes a kind of trend using glass material.It is well known that glass it is smooth easily fall, it is broken and broken
After hurt sb.'s feelings risk, so be badly in need of it is a kind of can reduce its broken probability and the scattered product of fragment can be prevented after broken, also
It is asked to influence the overall sense organ of mobile phone glass bonnet.
The content of the invention
This uses OCA optical cements to solve the above problems the invention provides explosion-proof in a kind of mobile phone, and service life is long, environmental protection
Effect is good, and saves the energy, moderate.
The technical scheme that the present invention is provided is:It is explosion-proof in a kind of mobile phone to use OCA optical cements, by following mass percentage content
Material it is reacted after be made:
By said components, example is sequentially added in stirred tank by mass percentage, natural after being mixed evenly under the conditions of lucifuge
Stand froth breaking and glue is made, then by the glue application one side that sided corona treatment is crossed on PET mould release membrances, enclose and lead to after silicon mould release membrance
Cross UV solidifications;
Wherein, acrylic polymer by the material of following weight/mass percentage composition it is reacted after be made:
The molecular weight regulator is in n-dodecyl mercaptan, tert-dodecylmercaotan, the different monooctyl ester of tri-thiol propionic acid
It is one or more;
First weigh 1/2 above-mentioned amount Isooctyl acrylate monomer add reactor, then weigh above-mentioned amount methyl methacrylate,
Methacrylic acid -2- ethylhexyls, hydroxy-ethyl acrylate, molecular weight regulator sequentially add in reactor and continue stirring,
Remaining 1/2 Isooctyl acrylate monomer for having dissolved azo dibutyronitrile is added drop-wise in reactor while heating to reactor material
And continuing stirring, reactor is warming up to 80~90 DEG C and is incubated 3 hours, then naturally cools to normal temperature.
As optimization, initiator is 1- hydroxycyclohexyl phenyl ketones or/and 2,4,6- trimethylbenzoy-diphenies
Phosphine oxide.
The beneficial effects of the present invention are explosion-proof in mobile phone to use OCA optical cements, service life is long, weatherability, yellowing resistance
Good, environmental protection effect is good, excellent performance, moderate.
Embodiment
Embodiment 1:
It is prepared by OCA optical cements:
By said components, example is added in stirred tank by mass percentage, is stood naturally after being mixed evenly under the conditions of lucifuge
Glue is made in froth breaking, then by the glue application one side that sided corona treatment is crossed on PET mould release membrances, encloses after silicon mould release membrance by UV
Solidification;
Wherein, acrylic polymer by the material of following weight/mass percentage composition it is reacted after be made:
First weigh 1/2 above-mentioned amount Isooctyl acrylate monomer add reactor, then weigh above-mentioned amount methyl methacrylate,
Methacrylic acid -2- ethylhexyls, hydroxy-ethyl acrylate, n-dodecyl mercaptan sequentially add in reactor and continue stirring,
Remaining 1/2 Isooctyl acrylate monomer for having dissolved azo dibutyronitrile is added drop-wise to reactor while being heated up to reactor material
In and continue stirring, reactor be warming up to 80~90 DEG C and be incubated 3 hours, then naturally cool to normal temperature.
Embodiment 2:
It is prepared by OCA optical cements:
By said components, example is sequentially added in stirred tank by mass percentage, natural after being mixed evenly under the conditions of lucifuge
Stand froth breaking and glue is made, then by the glue application one side that sided corona treatment is crossed on PET mould release membrances, enclose after PET mould release membrances
Solidified by UV;
Wherein, acrylic polymer by the material of following weight/mass percentage composition it is reacted after be made:
First weigh 1/2 above-mentioned amount Isooctyl acrylate monomer add reactor, then weigh above-mentioned amount methyl methacrylate,
Methacrylic acid -2- ethylhexyls, hydroxy-ethyl acrylate, tert-dodecylmercaotan sequentially add in reactor and continue stirring,
Remaining 1/2 Isooctyl acrylate monomer for having dissolved azo dibutyronitrile is added drop-wise to reactor while being heated up to reactor material
In and continue stirring, reactor be warming up to 80~90 DEG C and be incubated 3 hours, then naturally cool to normal temperature.
Embodiment 3:
By said components, example is sequentially added in stirred tank by mass percentage, natural after being mixed evenly under the conditions of lucifuge
Stand froth breaking and glue is made, then by the glue application one side that sided corona treatment is crossed on PET mould release membrances, enclose and lead to after silicon mould release membrance
Cross UV solidifications;
Wherein, acrylic polymer by the material of following weight/mass percentage composition it is reacted after be made:
First weigh 1/2 above-mentioned amount Isooctyl acrylate monomer add reactor, then weigh above-mentioned amount methyl methacrylate,
Methacrylic acid -2- ethylhexyls, hydroxy-ethyl acrylate, agent sequentially add in reactor and continue stirring, are giving reactor thing
Remaining 1/2 Isooctyl acrylate monomer for having dissolved azo dibutyronitrile is added drop-wise in reactor and persistently stirred while material heating
Mix, reactor is warming up to 80~90 DEG C and is incubated 3 hours, then naturally cools to normal temperature.
The present invention is explained in detail above in conjunction with embodiment, but the present invention is not limited to above-described embodiment.In ability
, can also be on the basis of each composition effect basis mechanism is well understood that in the knowledge that domain those of ordinary skill possesses
Do not depart from the premise of present inventive concept that various changes can be made, come under protection scope of the present invention.
Claims (2)
1. explosion-proof in a kind of mobile phone use OCA optical cements, by the material of following mass percentage content it is reacted after be made:
Acrylic polymer 50 ~ 80%
Isobornyl methacrylate 5 ~ 40%
Ethyl acrylate 10 ~ 25%
Initiator 0.1 ~ 5%
By said components, example is added in stirred tank by mass percentage, stands froth breaking after being mixed evenly under the conditions of lucifuge naturally
Glue is made, then by the glue application one side that sided corona treatment is crossed on PET mould release membrances, encloses solid by UV after PET mould release membrances
Change;
Wherein, acrylic polymer by the material of following weight/mass percentage composition it is reacted after be made:
Isooctyl acrylate monomer 20 ~ 60%
Methyl methacrylate 10 ~ 35%
Methacrylic acid -2- ethylhexyls 10 ~ 35%
Hydroxy-ethyl acrylate 3 ~ 8%
Molecular weight regulator 3 ~ 8%
Azo dibutyronitrile 0.1 ~ 2%
The molecular weight regulator is one kind in n-dodecyl mercaptan, tert-dodecylmercaotan, the different monooctyl ester of tri-thiol propionic acid
Or it is a variety of;
The Isooctyl acrylate monomer for first weighing 1/2 above-mentioned amount adds reactor, then weighs the methyl methacrylate of above-mentioned amount, methyl
Acrylic acid-2-ethyl caproite, hydroxy-ethyl acrylate, molecular weight regulator sequentially add in reactor and continue stirring, to anti-
Remaining 1/2 Isooctyl acrylate monomer for having dissolved azo dibutyronitrile is added drop-wise in reactor and held while answering kettle material to heat up
Continuous stirring, reactor is warming up to 80 ~ 90 DEG C and is incubated 3 hours, then naturally cools to normal temperature.
2. explosion-proof in mobile phone according to claim 1 use OCA optical cements, it is characterised in that:Initiator is 1- hydroxy cyclohexylphenyls
Base phenyl ketone or/and 2,4,6- trimethylbenzoy-dipheny phosphine oxides.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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CN201710281396.5A CN106978112A (en) | 2017-04-26 | 2017-04-26 | It is explosion-proof in a kind of mobile phone to use OCA optical cements |
Applications Claiming Priority (1)
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CN201710281396.5A CN106978112A (en) | 2017-04-26 | 2017-04-26 | It is explosion-proof in a kind of mobile phone to use OCA optical cements |
Publications (1)
Publication Number | Publication Date |
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CN106978112A true CN106978112A (en) | 2017-07-25 |
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CN201710281396.5A Pending CN106978112A (en) | 2017-04-26 | 2017-04-26 | It is explosion-proof in a kind of mobile phone to use OCA optical cements |
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107858109A (en) * | 2017-10-31 | 2018-03-30 | 芜湖辉灿电子科技有限公司 | Explosion-proof OCA optical cements in a kind of mobile phone |
CN107880790A (en) * | 2017-11-29 | 2018-04-06 | 深圳市东魔科技有限公司 | Glue composition |
CN107955548A (en) * | 2017-10-31 | 2018-04-24 | 芜湖辉灿电子科技有限公司 | A kind of mobile phone screen anti-blue light OCA optical cements |
CN112195003A (en) * | 2020-10-12 | 2021-01-08 | 世星科技股份有限公司 | OCA optical cement, preparation method and application thereof |
CN112210327A (en) * | 2020-10-12 | 2021-01-12 | 世星科技股份有限公司 | OCA optical cement, preparation method and application thereof |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104194656A (en) * | 2014-07-17 | 2014-12-10 | 华南理工大学 | Acrylic ester optical cement and preparation method thereof |
-
2017
- 2017-04-26 CN CN201710281396.5A patent/CN106978112A/en active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104194656A (en) * | 2014-07-17 | 2014-12-10 | 华南理工大学 | Acrylic ester optical cement and preparation method thereof |
Non-Patent Citations (1)
Title |
---|
李红强 主编: "《胶粘原理、技术及应用》", 31 January 2014 * |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107858109A (en) * | 2017-10-31 | 2018-03-30 | 芜湖辉灿电子科技有限公司 | Explosion-proof OCA optical cements in a kind of mobile phone |
CN107955548A (en) * | 2017-10-31 | 2018-04-24 | 芜湖辉灿电子科技有限公司 | A kind of mobile phone screen anti-blue light OCA optical cements |
CN107880790A (en) * | 2017-11-29 | 2018-04-06 | 深圳市东魔科技有限公司 | Glue composition |
CN112195003A (en) * | 2020-10-12 | 2021-01-08 | 世星科技股份有限公司 | OCA optical cement, preparation method and application thereof |
CN112210327A (en) * | 2020-10-12 | 2021-01-12 | 世星科技股份有限公司 | OCA optical cement, preparation method and application thereof |
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PB01 | Publication | ||
PB01 | Publication | ||
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Application publication date: 20170725 |