CN106554729A - A kind of fogless shadow Protection glue band and preparation method thereof - Google Patents
A kind of fogless shadow Protection glue band and preparation method thereof Download PDFInfo
- Publication number
- CN106554729A CN106554729A CN201610994876.1A CN201610994876A CN106554729A CN 106554729 A CN106554729 A CN 106554729A CN 201610994876 A CN201610994876 A CN 201610994876A CN 106554729 A CN106554729 A CN 106554729A
- Authority
- CN
- China
- Prior art keywords
- protection glue
- monomer
- glue band
- fogless
- sensitive adhesive
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Classifications
-
- 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
- C08F2/00—Processes of polymerisation
- C08F2/12—Polymerisation in non-solvents
- C08F2/16—Aqueous medium
- C08F2/22—Emulsion polymerisation
- C08F2/24—Emulsion polymerisation with the aid of emulsifying agents
- C08F2/26—Emulsion polymerisation with the aid of emulsifying agents anionic
-
- 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
- C08F2/00—Processes of polymerisation
- C08F2/12—Polymerisation in non-solvents
- C08F2/16—Aqueous medium
- C08F2/22—Emulsion polymerisation
- C08F2/24—Emulsion polymerisation with the aid of emulsifying agents
- C08F2/30—Emulsion polymerisation with the aid of emulsifying agents non-ionic
-
- 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
- C08F265/06—Polymerisation of acrylate or methacrylate esters on to polymers thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/29—Compounds containing one or more carbon-to-nitrogen double bonds
-
- 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
- C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
- C09J11/02—Non-macromolecular additives
- C09J11/06—Non-macromolecular additives organic
-
- 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
- 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
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
- C09J7/22—Plastics; Metallised plastics
-
- 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
- C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
- C09J7/38—Pressure-sensitive adhesives [PSA]
-
- 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
- C09J2423/00—Presence of polyolefin
- C09J2423/04—Presence of homo or copolymers of ethene
- C09J2423/046—Presence of homo or copolymers of ethene in the substrate
-
- 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
Abstract
The present invention relates to a kind of fogless shadow Protection glue band and preparation method thereof, the Protection glue band is obtained by substrate layer pressure-sensitive adhesive coating;Wherein, pressure sensitive adhesive by soft monomer, hard monomer, functional monomer the emulsion polymerization in the presence of emulsifying agent, be eventually adding initiator and firming agent prepared.Relative molecular weight and the degree of cross linking of the present invention by control polymer, it is achieved thereby that suppressing or reducing the migration of adhesive small molecular material, solve Protection glue band " mist shadow " problem to a certain extent, have a good application prospect.
Description
Technical field
The invention belongs to industrial products protection field, more particularly to a kind of fogless shadow Protection glue band and preparation method thereof.
Background technology
During Protection glue band is widely used in industrial processes and industrial products final protection field, for interim protection
Part or product surface, prevent cut or stain, final to be removed from surface is pasted again.This special purposes is determined
Protecting film must possess following performance:First, to needing surface to be protected to have fabulous adhesion;2nd, needing to remove
When can with minimum peeling force from by protection surface easy removal, and ensure do not leave any vestige;3rd, protected by guard period
Retaining tape will not cause because of self deterioration product surface contaminated or damage.
Protection glue band leaves " mist shadow " after removing be that Protection glue band is common in application process and very scabrous pollution
Problem, specifically refers to Protection glue band and is pasted be retained in after surface removes by the shallow mist on patch surface, but not cull.It is this
Specifically now it is that surface of plastic products in mirror face stainless steel, bright face is particularly evident, this brings greatly tired to product protection
Disturb, serious even can scrap products.It has been generally acknowledged that " mist shadow " be Protection glue with the low molecule quality material in adhesive from glue
Layer is to being caused by patch surface migration, therefore to reduce the content of low molecule quality material in adhesive be that to solve " mist shadow " most practical
Effective method.
At present, the method for comparing main flow is to prepare the protection that Protection glue band is used as bright Flour product using coextruding method, so as to
" mist shadow " problem of solution.
The content of the invention
The technical problem to be solved is to provide a kind of fogless shadow Protection glue band and preparation method thereof, the Protection glue
Relative molecular weight and the degree of cross linking of the band by control polymer, it is achieved thereby that suppressing or reducing adhesive small molecular material
Migration, solve Protection glue band " mist shadow " problem to a certain extent, have a good application prospect.
A kind of fogless shadow Protection glue band of the present invention, the Protection glue band are obtained by substrate layer pressure-sensitive adhesive coating;Wherein, press
Quick glue emulsion polymerization in the presence of emulsifying agent by soft monomer, hard monomer, functional monomer, is eventually adding initiator and firming agent
Prepare.
The substrate layer is made up of the polyethylene PE film that Jing sided corona treatments are crossed.
The soft monomer be butyl acrylate BA, Isooctyl acrylate monomer 2-EHA it is therein one or two.Soft monomer is referred to
The relatively low monomer of vitrification point, acts primarily as adhesive attraction, gives pressure sensitive adhesive to the sufficiently high wettability of base material and adhesiveness.
The hard monomer be methyl methacrylate MMA, vinylacetate VAc, acrylic acid methyl ester. MA it is therein a kind of or
It is several.Hard monomer is also called interior polycondensation monomer, is the monomer with higher vitrification point Tg.Can produce after itself and soft monomer copolymerization
It is raw that there is preferable cohesive strength and the copolymer compared with operation at high temperature, the addition of such monomer, adhesive not only can be improved
Cohesiveness, and resistance to water, adhesive strength, transparency etc. are also obviously improved.
The functional monomer is (methyl) 2-(Acryloyloxy)ethanol HEMA, acrylamide AM, acrylic acid AA one kind therein
Or it is several.Function monomer is also called cross-linking monomer, is the monomer with various functional groups.The introducing of functional group significantly can be carried
The cohesive strength and adhesive property of high adhesive, gives adhesive response characteristic, such as hydrophilic, thermostability and bridging property etc..When
When functional monomer is that three mixes, acrylic acid content is 2-4%, and 2-(Acryloyloxy)ethanol content is 4-8%, acrylamide content
For 0.3-0.6%.
The emulsifying agent is mass ratio 1:4~2:1 anion surfactant and nonionic surfactant;Emulsifying agent
Consumption for polymerized monomer total amount 3-5% (mass percent).
For the environment that is suitably polymerized, it is necessary to select suitable emulsifying agent, during emulsifying agent is emulsion polymerization systems
Important component, in general it and be not involved in reaction, but it to the rate of polymerization in emulsion polymerization, emulsion particle size with
And the heat stability of distribution of sizes, synthetic polymer has significant impact, it also affects the polymer for determining polymer performance
Molecular weight and molecular weight distribution, thus the selection of emulsifying agent is particularly significant.The present invention have selected composite emulsifying system, adopt
It is composited with sodium lauryl sulphate and alkylphenol polyoxyethylene.
The initiator is inorganic peroxide;0.2%-0.6% (quality of the consumption of initiator for polymerized monomer total amount
Percentage ratio).Preferably potassium peroxydisulfate of the invention.
The firming agent is isocyanates firming agent;5-9% (quality of the consumption of firming agent for polymer emulsion total amount
Percentage ratio).Isocyanates firming agent includes toluene di-isocyanate(TDI), methyl diphenylene diisocyanate, 1,6- oneself two isocyanides
Acid esters etc., the present invention preferably 1, hexamethylene-diisocyanate is used as firming agent.
A kind of preparation method of the fogless shadow Protection glue band of the present invention, including:
(1) emulsifying agent and deionized water are taken, is uniformly mixed;80 DEG C are then heated to, mix monomer 1 is added, is obtained A
Component;Using initiator solution as B component;By two components of A, B simultaneously to Deca in reactor, (now temperature is still for insulation
For 80 DEG C) cooling discharge after 1~2h, obtain pressure sensitive adhesive core;
The mix monomer 1 is consisted of:By mass percentage, butyl acrylate BA 64%-80%, methacrylic acid
Methyl ester MMA 12-25%, acrylic acid methyl ester. MA 2%-15%;
(2) take above-mentioned pressure sensitive adhesive core to pour in reactor, stirring is warming up to 85 DEG C, while Deca mix monomer 2 and initiation
Agent aqueous solution, after 1~2h of insulation, (now temperature is still 85 DEG C) cooling discharge, obtains nucleocapsid pressure-sensitive adhesive emulsion;
The mix monomer 2 is consisted of:By mass percentage, butyl acrylate BA 40%-48%, methacrylic acid
Methyl ester MMA 15%-25%, 2-(Acryloyloxy)ethanol 12%-18%, acrylic acid AA 0.5-2.5%, vinylacetate VAc10%-
20%, acrylic acid methyl ester. MA 3%-9%;
(3) obtained nucleocapsid pressure-sensitive adhesive emulsion is added into firming agent, after mixing, is coated in the PE thin film that Jing sided corona treatments are crossed
On, solidification obtains Protection glue band parent roll, and finally cutting obtains final product fogless shadow Protection glue band;.
Solidification in the step (3) is specially:80 DEG C of solidification 5min, 40 DEG C of resolidifications the residual moistures that volatilize.
Pressure sensitive adhesive of the present invention is synthesized using emulsion polymerization technology.The technology relative maturity of emulsion polymerization, so as to
Water-borne pressure sensitive adhesive for synthesized high-performance provides technical guarantee.The pressure sensitive adhesive of emulsion-type not only remains pressure sensitive adhesive and preferably presses
Quick performance, preferably, and emulsion polymerization Theory comparison is perfect for environment-friendly type, and production technology is ripe, course of reaction have controllability and
Designability, by changing polymerization technique, can give emulsion polymer with specified molecular weight and its distribution, specific latex particle size
And its distribution and specific emulsion particle form, so as to prepare the adhesive of different properties, this is carried for synthetic emulsion type pressure sensitive adhesive
Technical guarantee is supplied.
In order to realize foregoing invention, the present invention prepares interior hard outer soft nucleocapsid using the method for nucleocapsid seeded emulsion polymerization
Structure micelle, i.e., vitrification point Tg of the polymer that vitrification point Tg of the polymer first prepared is prepared after being more than,
Cross-linking agent is added before and after preparation while polymer simultaneously, makes cross-linking agent the inside of polymer is evenly distributed in come in improving
Poly- power.
Beneficial effect
Relative molecular weight and the degree of cross linking of the present invention by control polymer, it is achieved thereby that suppressing or reducing adhesive
The migration of small molecular material, solves Protection glue band " mist shadow " problem to a certain extent, has a good application prospect.Such as
In the protection of the bright panel of automobile door and window, generally, the material of bright panel is 403,304 mirror face stainless steels, common pressure-sensitive Protection glue
Band after pasting through illumination, the change of heat easily form " mist shadow " on surface stainless steel and the product prepared by the present invention then not
Above-mentioned condition occurs.
Specific embodiment
With reference to specific embodiment, the present invention is expanded on further.It should be understood that these embodiments are merely to illustrate the present invention
Rather than limit the scope of the present invention.In addition, it is to be understood that after the content for having read instruction of the present invention, people in the art
Member can be made various changes or modifications to the present invention, and these equivalent form of values equally fall within the application appended claims and limited
Scope.
Embodiment 1
(1) preparation of pressure sensitive adhesive core:
Emulsifying agent and deionized water are taken, 30min mix homogeneously is stirred;80 DEG C are then heated to, mix monomer 1 is added, is obtained
To component A, take out and load funnel, it is standby;Using initiator solution as B component, load another funnel, it is standby;By A, B two
Component is simultaneously to Deca in reactor, it is ensured that dripped off in 3 hours, cooling discharge after insulation 1h, obtains pressure sensitive adhesive core;
The mix monomer 1 is consisted of:By mass percentage, butyl acrylate BA 75%, methyl methacrylate
MMA 18%, acrylic acid methyl ester. MA 7%;
Emulsifying agent is mass ratio 1:4 sodium lauryl sulphate and alkylphenol polyoxyethylene, addition are polymerized monomer
The 3.5% of total amount;
Initiator is potassium peroxydisulfate, and addition is the 0.6% of polymerized monomer total amount;
(2) preparation of nucleocapsid pressure-sensitive adhesive emulsion:
Take above-mentioned pressure sensitive adhesive core to pour in reactor, stirring is warming up to 85 DEG C, while Deca mix monomer 2 and initiator water
Solution, Deca control are dripped off in 2h, cooling discharge after insulation 1h, obtain nucleocapsid pressure-sensitive adhesive emulsion;
The mix monomer 2 is consisted of:By mass percentage, butyl acrylate BA 40%, methyl methacrylate
MMA 21%, 2-(Acryloyloxy)ethanol HEMA 15%, acrylic acid AA 1%, vinylacetate VAc 17%, acrylic acid methyl ester. MA
6%;
The same step of emulsifying agent (1), addition for polymerized monomer total amount 3.5%;
The same step of initiator (1), addition for polymerized monomer total amount 0.6%;
(3) isocyanate curing agent that obtained nucleocapsid pressure-sensitive adhesive emulsion adds emulsion gross mass 5% is taken, after mixing, is applied
Apply on the PE thin film crossed in Jing sided corona treatments, 80 DEG C solidification 5min, 40 DEG C fully solidify and volatilize residual moisture 48h after, obtain
Dry glue thickness is the Protection glue band parent roll of (5 ± 1) μm, cuts into required width and obtains final product fogless shadow Protection glue band.
Obtained fogless shadow Protection glue band is shown in Table 1 according to national standard test result.
Embodiment 2
(1) preparation of pressure sensitive adhesive core:
Emulsifying agent and deionized water are taken, 30min mix homogeneously is stirred;80 DEG C are then heated to, mix monomer 1 is added, is obtained
To component A, take out and load funnel, it is standby;Using initiator solution as B component, load another funnel, it is standby;By A, B two
Component is simultaneously to Deca in reactor, it is ensured that dripped off in 3 hours, cooling discharge after insulation 1h, obtains pressure sensitive adhesive core;
The mix monomer 1 is consisted of:By mass percentage, butyl acrylate BA 75%, methyl methacrylate
MMA 20%, acrylic acid methyl ester. MA 5%;
Emulsifying agent is mass ratio 1:2 sodium lauryl sulphate and alkylphenol polyoxyethylene, addition are polymerized monomer
The 3.5% of total amount;
Initiator is potassium peroxydisulfate, and addition is the 0.6% of polymerized monomer total amount;
(2) preparation of nucleocapsid pressure-sensitive adhesive emulsion:
Take above-mentioned pressure sensitive adhesive core to pour in reactor, stirring is warming up to 85 DEG C, while Deca mix monomer 2 and initiator water
Solution, Deca control are dripped off in 2h, cooling discharge after insulation 1h, obtain nucleocapsid pressure-sensitive adhesive emulsion;
The mix monomer 2 is consisted of:By mass percentage, butyl acrylate BA 40%, methyl methacrylate
MMA 17%, 2-(Acryloyloxy)ethanol HEMA 17.5%, acrylic acid AA 0.5%, vinylacetate VAc 19%, acrylic acid methyl ester.
MA 6%;
The same step of emulsifying agent (1), addition for polymerized monomer total amount 3.5%;
The same step of initiator (1), addition for polymerized monomer total amount 0.6%;
(3) isocyanate curing agent that obtained nucleocapsid pressure-sensitive adhesive emulsion adds emulsion gross mass 9% is taken, after mixing, is applied
Apply on the PE thin film crossed in Jing sided corona treatments, 80 DEG C solidification 5min, 40 DEG C fully solidify and volatilize residual moisture 48h after, obtain
Dry glue thickness is the Protection glue band parent roll of (5 ± 1) μm, cuts into required width and obtains final product fogless shadow Protection glue band.
Obtained fogless shadow Protection glue band is shown in Table 1 according to national standard test result.
Embodiment 3
(1) preparation of pressure sensitive adhesive core:
Emulsifying agent and deionized water are taken, 30min mix homogeneously is stirred;80 DEG C are then heated to, mix monomer 1 is added, is obtained
To component A, take out and load funnel, it is standby;Using initiator solution as B component, load another funnel, it is standby;By A, B two
Component is simultaneously to Deca in reactor, it is ensured that dripped off in 3 hours, cooling discharge after insulation 1h, obtains pressure sensitive adhesive core;
The mix monomer 1 is consisted of:By mass percentage, butyl acrylate BA 70%, methyl methacrylate
MMA 24%, acrylic acid methyl ester. MA 6%;
Emulsifying agent is mass ratio 2:1 sodium lauryl sulphate and alkylphenol polyoxyethylene, addition are polymerized monomer
The 3.5% of total amount;
Initiator is potassium peroxydisulfate, and addition is the 0.6% of polymerized monomer total amount;
(2) preparation of nucleocapsid pressure-sensitive adhesive emulsion:
Take above-mentioned pressure sensitive adhesive core to pour in reactor, stirring is warming up to 85 DEG C, while Deca mix monomer 2 and initiator water
Solution, Deca control are dripped off in 2h, cooling discharge after insulation 1h, obtain nucleocapsid pressure-sensitive adhesive emulsion;
The mix monomer 2 is consisted of:By mass percentage, butyl acrylate BA 40%, methyl methacrylate
MMA 17%, 2-(Acryloyloxy)ethanol HEMA 17.5%, acrylic acid AA 1.5%, vinylacetate VAc 17%, acrylic acid methyl ester.
MA 7%;
The same step of emulsifying agent (1), addition for polymerized monomer total amount 3.5%;
The same step of initiator (1), addition for polymerized monomer total amount 0.6%;
(3) isocyanate curing agent that obtained nucleocapsid pressure-sensitive adhesive emulsion adds emulsion gross mass 8% is taken, after mixing, is applied
Apply on the PE thin film crossed in Jing sided corona treatments, 80 DEG C solidification 5min, 40 DEG C fully solidify and volatilize residual moisture 48h after, obtain
Dry glue thickness is the Protection glue band parent roll of (5 ± 1) μm, cuts into required width and obtains final product fogless shadow Protection glue band.
Obtained fogless shadow Protection glue band is shown in Table 1 according to national standard test result.
Embodiment 4
(1) preparation of pressure sensitive adhesive core:
Emulsifying agent and deionized water are taken, 30min mix homogeneously is stirred;80 DEG C are then heated to, mix monomer 1 is added, is obtained
To component A, take out and load funnel, it is standby;Using initiator solution as B component, load another funnel, it is standby;By A, B two
Component is simultaneously to Deca in reactor, it is ensured that dripped off in 3 hours, cooling discharge after insulation 1h, obtains pressure sensitive adhesive core;
The mix monomer 1 is consisted of:By mass percentage, butyl acrylate BA 66%, methyl methacrylate
MMA 24%, acrylic acid methyl ester. MA 10%;
Emulsifying agent is mass ratio 1:1 sodium lauryl sulphate and alkylphenol polyoxyethylene, addition are polymerized monomer
The 3.5% of total amount;
Initiator is potassium peroxydisulfate, and addition is the 0.6% of polymerized monomer total amount;
(2) preparation of nucleocapsid pressure-sensitive adhesive emulsion:
Take above-mentioned pressure sensitive adhesive core to pour in reactor, stirring is warming up to 85 DEG C, while Deca mix monomer 2 and initiator water
Solution, Deca control are dripped off in 2h, cooling discharge after insulation 1h, obtain nucleocapsid pressure-sensitive adhesive emulsion;
The mix monomer 2 is consisted of:By mass percentage, butyl acrylate BA 45%, methyl methacrylate
MMA 22%, 2-(Acryloyloxy)ethanol HEMA 13%, acrylic acid AA 2.0%, vinylacetate VAc 11%, acrylic acid methyl ester. MA
7%;
The same step of emulsifying agent (1), addition for polymerized monomer total amount 3.5%;
The same step of initiator (1), addition for polymerized monomer total amount 0.6%;
(3) isocyanate curing agent that obtained nucleocapsid pressure-sensitive adhesive emulsion adds emulsion gross mass 6% is taken, after mixing, is applied
Apply on the PE thin film crossed in Jing sided corona treatments, 80 DEG C solidification 5min, 40 DEG C fully solidify and volatilize residual moisture 48h after, obtain
Dry glue thickness is the Protection glue band parent roll of (5 ± 1) μm, cuts into required width and obtains final product fogless shadow Protection glue band.
Obtained fogless shadow Protection glue band is shown in Table 1 according to national standard test result.
Embodiment 5
(1) preparation of pressure sensitive adhesive core:
Emulsifying agent and deionized water are taken, 30min mix homogeneously is stirred;80 DEG C are then heated to, mix monomer 1 is added, is obtained
To component A, take out and load funnel, it is standby;Using initiator solution as B component, load another funnel, it is standby;By A, B two
Component is simultaneously to Deca in reactor, it is ensured that dripped off in 3 hours, cooling discharge after insulation 1h, obtains pressure sensitive adhesive core;
The mix monomer 1 is consisted of:By mass percentage, butyl acrylate BA 80%, methyl methacrylate
MMA 18%, acrylic acid methyl ester. MA 2%;
Emulsifying agent is mass ratio 1:3 sodium lauryl sulphate and alkylphenol polyoxyethylene, addition are polymerized monomer
The 3.5% of total amount;
Initiator is potassium peroxydisulfate, and addition is the 0.6% of polymerized monomer total amount;
(2) preparation of nucleocapsid pressure-sensitive adhesive emulsion:
Take above-mentioned pressure sensitive adhesive core to pour in reactor, stirring is warming up to 85 DEG C, while Deca mix monomer 2 and initiator water
Solution, Deca control are dripped off in 2h, cooling discharge after insulation 1h, obtain nucleocapsid pressure-sensitive adhesive emulsion;
The mix monomer 2 is consisted of:By mass percentage, butyl acrylate BA 45%, methyl methacrylate
MMA 22%, 2-(Acryloyloxy)ethanol HEMA 11.5%, acrylic acid AA 2.5%, vinylacetate VAc 10%, acrylic acid methyl ester.
MA 9%;
The same step of emulsifying agent (1), addition for polymerized monomer total amount 3.5%;
The same step of initiator (1), addition for polymerized monomer total amount 0.6%;
(3) isocyanate curing agent that obtained nucleocapsid pressure-sensitive adhesive emulsion adds emulsion gross mass 7% is taken, after mixing, is applied
Apply on the PE thin film crossed in Jing sided corona treatments, 80 DEG C solidification 5min, 40 DEG C fully solidify and volatilize residual moisture 48h after, obtain
Dry glue thickness is the Protection glue band parent roll of (5 ± 1) μm, cuts into required width and obtains final product fogless shadow Protection glue band.
Obtained fogless shadow Protection glue band is shown in Table 1 according to national standard test result.
Table 1
Claims (8)
1. a kind of fogless shadow Protection glue band, it is characterised in that:The Protection glue band is obtained by substrate layer pressure-sensitive adhesive coating;Wherein,
Pressure sensitive adhesive emulsion polymerization in the presence of emulsifying agent by soft monomer, hard monomer, functional monomer, is eventually adding initiator and solidification
Agent is prepared.
2. a kind of fogless shadow Protection glue band according to claim 1, it is characterised in that:The substrate layer is by Jing sided corona treatments
The polyethylene PE film composition crossed.
3. a kind of fogless shadow Protection glue band according to claim 1, it is characterised in that:The soft monomer is butyl acrylate
BA, Isooctyl acrylate monomer 2-EHA it is therein one or two;The hard monomer is methyl methacrylate MMA, vinylacetate
VAc, acrylic acid methyl ester. MA it is therein one or more;The functional monomer be 2-(Acryloyloxy)ethanol HEMA, acrylamide AM,
Acrylic acid AA it is therein one or more.
4. a kind of fogless shadow Protection glue band according to claim 1, it is characterised in that:The emulsifying agent is mass ratio 1:4
~2:1 anion surfactant and nonionic surfactant;3-5% of the consumption of emulsifying agent for polymerized monomer total amount.
5. a kind of fogless shadow Protection glue band according to claim 1, it is characterised in that:The initiator is inorganic peroxygen
Thing;0.2%-0.6% of the consumption of initiator for polymerized monomer total amount.
6. a kind of fogless shadow Protection glue band according to claim 1, it is characterised in that:The firming agent is isocyanates
Firming agent;0.4-0.9% of the consumption of firming agent for polymer emulsion total amount.
7. a kind of preparation method of fogless shadow Protection glue band, including:
(1) emulsifying agent and deionized water are taken, is uniformly mixed;80 DEG C are then heated to, mix monomer 1 is added, is obtained A groups
Point;Using initiator solution as B component;By two components of A, B simultaneously to Deca in reactor, lower the temperature after 1~2h of insulation
Material, obtains pressure sensitive adhesive core;
The mix monomer 1 is consisted of:By mass percentage, butyl acrylate 64%-80%, methyl methacrylate 12-
25%, acrylic acid methyl ester. 2%-15%;
(2) take above-mentioned pressure sensitive adhesive core to pour in reactor, stirring is warming up to 85 DEG C, while Deca mix monomer 2 and initiator water
Solution, cooling discharge after 1~2h of insulation, obtains nucleocapsid pressure-sensitive adhesive emulsion;
The mix monomer 2 is consisted of:By mass percentage, butyl acrylate 40%-48%, methyl methacrylate
15%-25%, 2-(Acryloyloxy)ethanol 12%-18%, acrylic acid 0.5-2.5%, vinylacetate 10%-20%, acrylic acid first
Ester 3%-9%;
(3) obtained nucleocapsid pressure-sensitive adhesive emulsion is coated on the PE thin film that Jing sided corona treatments are crossed, is solidified, obtain Protection glue band female
Volume, finally cutting obtain final product fogless shadow Protection glue band.
8. the preparation method of a kind of fogless shadow Protection glue band according to claim 7, it is characterised in that:The step (3)
In solidification be specially:80 DEG C of solidification 5min, 40 DEG C of resolidifications the residual moistures that volatilize.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610994876.1A CN106554729A (en) | 2016-11-11 | 2016-11-11 | A kind of fogless shadow Protection glue band and preparation method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610994876.1A CN106554729A (en) | 2016-11-11 | 2016-11-11 | A kind of fogless shadow Protection glue band and preparation method thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
CN106554729A true CN106554729A (en) | 2017-04-05 |
Family
ID=58444142
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201610994876.1A Pending CN106554729A (en) | 2016-11-11 | 2016-11-11 | A kind of fogless shadow Protection glue band and preparation method thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN106554729A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109233728A (en) * | 2018-08-01 | 2019-01-18 | 深圳日高胶带新材料有限公司 | A kind of Epoxy Resin Acrylate copolymerization pressure sensitive adhesive and preparation method thereof |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101434819A (en) * | 2008-12-10 | 2009-05-20 | 广东恒大新材料科技有限公司 | Aqueous adhesive for binding rubber and metal and preparation thereof |
CN102167773A (en) * | 2011-01-24 | 2011-08-31 | 南京夜视丽精细化工有限责任公司 | Acrylic acid emulsion and functional acrylic acid emulsion for unshadowed protective film |
CN102492379A (en) * | 2011-11-29 | 2012-06-13 | 广东达美新材料有限公司 | Fog-resistant aqueous pressure-sensitive adhesive and polyethylene protection film containing same |
CN104004477A (en) * | 2014-05-23 | 2014-08-27 | 华南理工大学 | Room temperature self-crosslinking polyacrylate pressure-sensitive adhesive and preparation method and application thereof |
CN105086886A (en) * | 2015-09-23 | 2015-11-25 | 广州宏昌胶粘带厂 | Single-component self-cross-linking high-temperature resistant emulsion pressure-sensitive adhesive and preparing method and application thereof |
-
2016
- 2016-11-11 CN CN201610994876.1A patent/CN106554729A/en active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101434819A (en) * | 2008-12-10 | 2009-05-20 | 广东恒大新材料科技有限公司 | Aqueous adhesive for binding rubber and metal and preparation thereof |
CN102167773A (en) * | 2011-01-24 | 2011-08-31 | 南京夜视丽精细化工有限责任公司 | Acrylic acid emulsion and functional acrylic acid emulsion for unshadowed protective film |
CN102492379A (en) * | 2011-11-29 | 2012-06-13 | 广东达美新材料有限公司 | Fog-resistant aqueous pressure-sensitive adhesive and polyethylene protection film containing same |
CN104004477A (en) * | 2014-05-23 | 2014-08-27 | 华南理工大学 | Room temperature self-crosslinking polyacrylate pressure-sensitive adhesive and preparation method and application thereof |
CN105086886A (en) * | 2015-09-23 | 2015-11-25 | 广州宏昌胶粘带厂 | Single-component self-cross-linking high-temperature resistant emulsion pressure-sensitive adhesive and preparing method and application thereof |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109233728A (en) * | 2018-08-01 | 2019-01-18 | 深圳日高胶带新材料有限公司 | A kind of Epoxy Resin Acrylate copolymerization pressure sensitive adhesive and preparation method thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN102504732B (en) | Solvent-based reticulated pressure-sensitive adhesive for polyethylene protective film and preparation method thereof | |
KR101833552B1 (en) | Double-sided pressure-sensitive adhesive tape | |
EP3075809B1 (en) | Adhesive resin composition | |
TWI404782B (en) | Pressure sensitive adhesive composition, product using the same, and display using the product | |
US20160122597A1 (en) | Preparation of pressure sensitive adhesive dispersions from multi-stage emulsion polymerization for applications of protective films | |
EP3412741A1 (en) | Uv-crosslinked hot-melt pressure-sensitive adhesive used for polyvinyl-chloride insulated adhesive tape | |
JP4984735B2 (en) | Acrylic adhesive manufacturing method | |
CN103952104A (en) | Solvent type pressure-sensitive adhesive used for polyethylene electronic protection film, and preparation method thereof | |
CN111527168B (en) | Method for producing glass unit and pressure-sensitive adhesive sheet | |
CN103524667A (en) | Water-based pressure-sensitive adhesive for polyethylene protection film and polyethylene protection film and preparation method thereof | |
CN105219316A (en) | A kind of high adhesion energy medical polyacrylate pressure-sensitive adhesive sticks agent | |
CN111234727A (en) | Waterborne environmental protection acrylic emulsion pressure sensitive adhesive protection film | |
CN113549415A (en) | High-solid-content strippable water-based pressure-sensitive adhesive and preparation method thereof | |
TWI415918B (en) | Adhesive composition for optical film protective sheet and protective film for optical film | |
CN111171250B (en) | Core-shell structure organic silicon internal crosslinking styrene-acrylic emulsion pressure-sensitive adhesive for protective film and preparation method and application thereof | |
EP2818486A1 (en) | Water-Dispersed Pressure-Sensitive Adhesive Composition and Method for Producing Same | |
CN102648261B (en) | Photocurable pressure-sensitive adhesive composition, photocurable pressure-sensitive adhesive layer, and photocurable pressure-sensitive adhesive sheet | |
CN112661900B (en) | Styrene-acrylic emulsion pressure-sensitive adhesive for protective film and preparation method thereof, styrene-acrylic emulsion pressure-sensitive adhesive tape for protective film and application thereof | |
CN106554729A (en) | A kind of fogless shadow Protection glue band and preparation method thereof | |
JP2001152118A (en) | Pressure-sensitive adhesive composition and pressure- sensitive adhesive tape | |
CN102695767B (en) | Adhesive composition and adhesive sheet | |
CN108285508B (en) | Medium-high viscosity emulsion type acrylate pressure-sensitive adhesive for protective film, and preparation method and application thereof | |
US20040213992A1 (en) | Electrically insulating material in tape form, insulated article and aqueous dispersion type acrylic pressure sensitive adhesive agent for insulating material | |
CN113429918B (en) | Single-component high-performance modified SBS water-based adhesive | |
EP3492543A1 (en) | Pressure-sensitive adhesive sheet |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20170405 |
|
RJ01 | Rejection of invention patent application after publication |