WO2005000989A1 - 表面保護フィルム用粘着剤および表面保護フィルム - Google Patents
表面保護フィルム用粘着剤および表面保護フィルム Download PDFInfo
- Publication number
- WO2005000989A1 WO2005000989A1 PCT/JP2004/006580 JP2004006580W WO2005000989A1 WO 2005000989 A1 WO2005000989 A1 WO 2005000989A1 JP 2004006580 W JP2004006580 W JP 2004006580W WO 2005000989 A1 WO2005000989 A1 WO 2005000989A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- sensitive adhesive
- component
- pressure
- peeling
- meth
- 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.)
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/62—Polymers of compounds having carbon-to-carbon double bonds
- C08G18/6216—Polymers of alpha-beta ethylenically unsaturated carboxylic acids or of derivatives thereof
- C08G18/622—Polymers of esters of alpha-beta ethylenically unsaturated carboxylic acids
- C08G18/6225—Polymers of esters of acrylic or methacrylic acid
- C08G18/6229—Polymers of hydroxy groups containing esters of acrylic or methacrylic acid with aliphatic polyalcohols
-
- 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
- C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
- C09J133/04—Homopolymers or copolymers of esters
- C09J133/14—Homopolymers or copolymers of esters of esters containing halogen, nitrogen, sulfur or oxygen atoms in addition to the carboxy oxygen
-
- 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
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
- C09J175/04—Polyurethanes
-
- 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
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
- C09J175/04—Polyurethanes
- C09J175/06—Polyurethanes from polyesters
-
- 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
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2170/00—Compositions for adhesives
- C08G2170/40—Compositions for pressure-sensitive adhesives
-
- 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
- C09J2203/00—Applications of adhesives in processes or use of adhesives in the form of films or foils
- C09J2203/306—Applications of adhesives in processes or use of adhesives in the form of films or foils for protecting painted surfaces, e.g. of cars
-
- 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
- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/30—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier
- C09J2301/302—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier the adhesive being pressure-sensitive, i.e. tacky at temperatures inferior to 30°C
-
- 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
- C09J2433/00—Presence of (meth)acrylic 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
- C09J2475/00—Presence of polyurethane
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer
Definitions
- the present invention relates to a pressure-sensitive adhesive for a surface protective film having excellent peelability, and more particularly, to a surface protective film having a small force required for peeling even at high speed peeling and having a small change in peeling force due to the peeling speed. It relates to an adhesive and a surface protection film using the same. Background art
- optical films are extremely large, such as polarizing plates, phase difference plates, and brightness enhancement films used for liquid crystal displays, AR films, electromagnetic wave shielding films, and IR cut films used for plasma displays.
- Optical films are laminated and used.
- these optical films Before the display is assembled, these optical films usually go through processes such as punching, transportation, and inspection, but during the process, the surface of the optical film is protected from scratches, dirt, etc. Usually, a surface protection film is attached.
- peeling force the force required for peeling
- the adhesive used for the surface protection film which is temporarily attached to protect the surface of plastic plates including films used in the display field, metal plates such as stainless steel, and glass plates, is acrylic.
- An adhesive is used.
- an acrylic pressure-sensitive adhesive a polymer obtained by copolymerizing a (meth) acrylate monomer and a monomer having a functional group in a side chain, and adding a crosslinking agent to the polymer is well known. ing.
- acrylic surface protective films those using an amide group and a hydroxyl group as the above functional groups and using a metal chelate compound and an isocyanate compound as a cross-linking agent have been proposed. Open 200-1-240830 public announcement). However, these surface protective films are intended to have little change in peeling force with time and to prevent blistering during heating, and the peeling force was not sufficiently small in high-speed peeling.
- the present inventors have conducted intensive studies in the above situation, and as a result, a pressure-sensitive adhesive having a specific polymer having a hydroxyl group as a functional group, a trifunctional or higher functional isocyanate-based crosslinking agent, and a specific gel fraction The inventors have found that the above-mentioned problems have been solved and completed the present invention.
- the present invention provides the following component (A) and component (B)
- the gel fraction is 90 mass% or more, the peeling force at a peeling speed of 30 OmmZ is 20 gf no inch or less, and the peeling force at a peeling speed of 2000 mm / min is 50 gf Z inch or less.
- Another object of the present invention is to provide a pressure-sensitive adhesive for surface protective films characterized by the following.
- the present invention also provides a surface protection film comprising the surface protection film adhesive applied to one surface of the surface protection film substrate.
- the (meth) acrylate copolymer used in the present invention (component The essential copolymerization component (a1) of (A)) is an alkyl acrylate having 12 or less carbon atoms in the alkyl group or an alkyl methacrylate having 12 or less carbon atoms in the alkyl group.
- the copolymer component (a1) include (meth) methyl acrylate, (meth) ethyl acrylate, (meth) propyl acrylate, (meth) butyl acrylate, and (meth) acrylic acid. Pentyl, hexyl (meth) acrylate, cyclohexyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, octyl (meth) acrylate, nonyl (meth) acrylate, ( (Meth) decyl acrylate, (me) dodecyl acrylate, and the like. One or more of these may be used.
- alkyl acrylate is preferable in order to adjust the glass transition temperature (Tg) of the component (A) obtained by copolymerization to a preferable range.
- the number of carbon atoms of the alkyl group of the component (a1) is preferably 4 to 10, and particularly preferably 8, in order to make the Tg of the component (A) a preferable value.
- 2-ethylhexyl acrylate is most preferred.
- the polymerization ratio of the copolymer component (a1) in the component (A) is 80 to 99% by mass (hereinafter simply referred to as "%"). If it is less than 80%, peeling may occur after pasting, and sufficient peelability may not be obtained at low speed and high speed peeling. If it is larger than 99%, the polymerization ratio of the other essential copolymerization component (a2) may be too low to obtain the gel fraction of the present invention. Preferably it is 90 to 98%, particularly preferably 92 to 96%.
- the other essential copolymer component (a2) of the component (A) is 4-hydroxybutyl acrylate or 4-hydroxybutyl methacrylate.
- This copolymerization component (a2) is a component having an alkyl group having 4 carbon atoms and having a hydroxyl group, and reacts with the later-described component (B) a trifunctional or higher functional isocyanate-based crosslinking agent to form a gel fraction. Adjust etc.
- a more preferred one is 4-hydroxybutyl. It's a luk relay.
- the 2-hydroxyethyl (meth) acrylate which also has a hydroxyl group but has 2 carbon atoms in the alkyl group, has low-speed (initial) peelability and high-speed peelability while satisfying other properties such as contamination. It is not possible to obtain an excellent surface protective film adhesive.
- the polymerization ratio of the copolymer component (a 2) in the component (A) is 1 to 10%.
- copolymerization component constituting the component (A) other copolymerization components can be used in addition to the above-mentioned essential copolymerization components (a1) and (a2).
- Other copolymerization components include aromatic vinyl monomers such as styrene, ⁇ -methylstyrene, and vinyltoluene; vinyl acetate; carboxyls such as (meth) acrylic acid, itaconic acid, crotonic acid, maleic acid, and fumaric acid.
- the polymerization ratio in the component (II) of the other copolymerization component is not particularly limited, but is preferably 5% or less.
- the content is preferably 2% or less. Since a polymer containing a functional group other than a hydroxyl group such as a carboxy group may deteriorate the low-speed (initial) peelability, it is not preferable to contain a large amount of such a group.
- the method of polymerizing the copolymer component (a 1) and the component (a 2) and, if necessary, other copolymer components for producing the acrylic copolymer as the component ( ⁇ ) is not particularly limited. Radical polymerization is preferred in terms of ease of polymer design, and contamination In view of the above, solution polymerization is particularly preferred.
- the molecular weight of the obtained component (A) is not particularly limited, but is preferably from 300,000 to 100,000 in terms of weight average molecular weight.
- preferred components (A) include those obtained by copolymerizing at least 90 to 99% of 2-ethylhexyl acrylate and 1 to 10% of 4-hydroxybutyl acrylate. Particularly preferred components (A) are 2-ethylhexyl acrylate 90 to 99%, 4-hydroxybutyl acrylate 1 to 10% and acrylic acid 0 to 1%. Things.
- the content of the component (A) with respect to the entire pressure-sensitive adhesive is not particularly limited, but is preferably from 80 to 99%, particularly preferably from 90 to 99%.
- the trifunctional or higher functional isocyanate crosslinking agent (component (B)) refers to a compound having three or more isocyanate groups in one molecule.
- the structure is not particularly limited, but specific examples thereof include tolylene diisocyanate, xylylene diisocyanate, chlorophenylene diisocyanate, hexamethylene diisocyanate, and tetramethylene diisocyanate.
- Diisocyanate compounds such as cyanate, isophorone diisocyanate, diphenylmethane diisocyanate, hydrogenated diphenylmethane diisocyanate, etc.
- cyanate isophorone diisocyanate
- diphenylmethane diisocyanate hydrogenated diphenylmethane diisocyanate
- polyisocyanate isocyanate compound
- burette-type compound and polyether polyol
- polyester polyol acrylic polyol
- polybutadiene polyol and polyisocyanate.
- Urethane prepolymers subjected to an addition reaction such as isoprene polyol Can Rukoto cited of Isoshiane Bok and the like.
- the components (B) preferred are tolylene diisocyanate, xylylene diisocyanate, or trimethylolpropane adduct of hexamethylene diisocyanate. These are used alone or in combination of two or more.
- the content of the component (B) is 1 to 5 parts with respect to 100 parts by weight of the component (A) (hereinafter simply referred to as “part”). If the content is more than 5 parts, the pot life of the adhesive may be deteriorated, and the adherend may be contaminated. If the amount is less than 1 part, the gel fraction may be low. Preferably, it is 2 to 5 parts, particularly preferably 2 to 4 parts.
- the pressure-sensitive adhesive for surface protective films of the present invention includes, in addition to the components (A) and (B), a component ( As C), a phosphate ester-based surfactant can be contained.
- a polyoxyethylene alkyl ether phosphate or a polyoxyethylene alkyl aryl ether phosphate is preferable.
- the alkyl group in the phosphoric acid ester molecule of poly (xylene ethylene alkyl ether) preferably has 8 to 18 carbon atoms, and particularly preferably 8 to 14 carbon atoms.
- the alkylaryl group in the phosphoric acid ester molecule of poly (xylene ethylenealkylaryl ether) is preferably an alkylphenyl group, and particularly preferably an n-nonylphenyl group.
- mono, di or triphosphate ester or a mixture thereof is used, and a monoester is preferable.
- the phosphate residue not having an ester bond may be a salt such as a sodium salt or a potassium salt, or may be hydrogen (as an acid). These are used alone or in combination of two or more.
- the content of the component (C) is not particularly limited.
- the amount is preferably from 1 to 10 parts, particularly preferably from 1 to 5 parts.
- the production of the pressure-sensitive adhesive of the present invention is carried out by mixing the component (A), the component (B) and, if necessary, the component (C) according to a conventional method.
- the pressure-sensitive adhesive of the present invention obtained as described above has a gel fraction of 90% or more.
- the definition of the gel fraction in the present invention is based on the description in the following examples. If the gel fraction is less than 90%, the adhesive strength at low speed and high speed peeling will be too high.
- the pressure-sensitive adhesive of the present invention has a peeling force at a peeling speed of 30 Omm / min of 2 Ogf / inch or less, and a peeling force at a peeling speed of 200 mm / min of 5 Of / inch or less. It is necessary to be.
- the definition of the peeling force of the pressure-sensitive adhesive in the present invention shall be based on the description in the following Examples, including the preparation of the surface protective film.
- the peeling force when peeled at 30 O mmZ shows low-speed peeling property, and the smaller the peeling force, the better the low-speed peeling property. Further, the peeling force when peeled for ZOOOOmmZ indicates high-speed peeling property, and the smaller the peeling force, the better the high-speed peeling property.
- a surface protective film By applying the pressure-sensitive adhesive of the present invention described above to one surface of a protective film base material, a surface protective film can be obtained.
- a polyester film such as polyethylene terephthalate (PET) or a plastic film such as polyethylene, polypropylene, or ethylene-vinyl acetate copolymer can be suitably used.
- the pressure-sensitive adhesive of the present invention dissolved in a solvent such as ethyl acetate, toluene, and methyl ethyl ketone is adjusted to a viscosity that allows easy application, and is evenly applied on a protective film base material. This is performed by drying and removing the solvent to cause a crosslinking reaction.
- a combination of a hydroxyl group-containing polymer and an isocyanate-based crosslinking agent has excellent low-speed release properties, but tends to have poor high-speed release properties.
- the combination of a polymer and an epoxy-based cross-linking agent has excellent high-speed release properties, but tends to be inferior in low-speed release properties.
- the pressure-sensitive adhesive of the present invention achieves both high-speed release properties and low-speed release properties by selecting the type of the hydroxyl group-containing polymer and the isocyanate-based cross-linking agent and the amounts thereof.
- the pressure-sensitive adhesive of the present invention is good in not only low-speed (initial) release property but also high-speed release property, and furthermore, the adherend is not contaminated and the pot life of the pressure-sensitive adhesive is good.
- the surface protective film using the pressure-sensitive adhesive of the present invention can be peeled from an adherend such as a panel without applying a strong force, so that there is little risk of damaging the adherend, and the peeling is also possible.
- the force changes little when peeling at high speed or when peeling at low speed, so that the efficiency does not decrease even when working manually.
- Production Example 2 A copolymer having a weight average molecular weight of 500,000 was prepared in the same manner as in Production Example 1 except that 4-hydroxybutyl acrylate (4 HBA) was replaced with 2-hydroxyethyl acrylate (2 HEA). A polymer was obtained. Hereinafter, it is referred to as acrylic polymer B.
- 4 HBA 4-hydroxybutyl acrylate
- 2 HEA 2-hydroxyethyl acrylate
- Coronate (a trifunctional crosslinking agent; Nippon Polyurethane Co., Ltd.) is added to an ethyl acetate solution of acrylic polymer A corresponding to an amount containing 100 parts of acrylic polymer A as a solid content. 4 parts were added and mixed to obtain an adhesive solution.
- the obtained pressure-sensitive adhesive solution was applied on a 50 m-thick polyethylene terephthalate (PET) film so that the thickness after drying became 20 m, and the solvent was removed at 80 ° C. It was dried and allowed to undergo a crosslinking reaction. Thereafter, a PET film coated with a silicone-coated film having a thickness of 38 m was stuck on the dried surface, and allowed to stand at 23 ° C and 65% RH for 7 days to obtain a surface protective film.
- PET polyethylene terephthalate
- a surface protection film was obtained in the same manner as in Example 1 except that 4 parts of duranate 24 A-100 (trifunctional cross-linking agent; manufactured by Asahi Kasei Corporation) was used as an isocyanate-based cross-linking agent.
- duranate 24 A-100 trifunctional cross-linking agent; manufactured by Asahi Kasei Corporation
- a surface protective film was obtained in the same manner as in Example 1 except that 0.5 part of Coronate L was used as an isocyanate-based crosslinking agent. Comparative Example 2
- a surface protection film was obtained in the same manner as in Example 1 except that 4 parts of tetrad X (manufactured by Mitsubishi Gas Chemical Co., Ltd.), an epoxy-based crosslinking agent, was used instead of the isocyanate-based crosslinking agent. Comparative Example 3
- a surface protective film was obtained in the same manner as in Example 1, except that 4 parts of aluminum chelate A (manufactured by Kawaken Fine Chemical Co., Ltd.), which is a metal chelate compound, was used instead of the isocyanate-based crosslinking agent. . Comparative Example 4
- a surface protective film was prepared in the same manner as in Example 1 except that the solution of acrylic polymer A was replaced with an ethyl acetate solution of acryl polymer B corresponding to an amount containing 100 parts of acrylic polymer B as a solid content. Obtained. Comparative Example 5
- Example 2 except that 5 parts of Desmodur N340 (manufactured by Sumika Bayer Urethane Co., Ltd.), which is a bifunctional isocyanate crosslinker, was used instead of 4 parts of the isocyanate crosslinker coronate. A surface protection film was obtained in the same manner as described above. Comparative Example 6
- Example 2 Same as Example 1 except that 6 parts of colonic acid L, an isocyanate-based crosslinking agent, was used Thus, a surface protective film was obtained.
- Test example 6 parts of colonic acid L, an isocyanate-based crosslinking agent, was used Thus, a surface protective film was obtained.
- Each of the above surface protection films was cut into 50 mm ⁇ 50 mm, the adhesive was peeled off from the cut surface protection film, and the initial weight of the adhesive was weighed.
- the adhesive was immersed in 100 g of ethyl acetate and left at room temperature for 24 hours. Thereafter, the mixture was filtered through a 200 mesh wire mesh, and the residue remaining on the mesh was dried at 80 ° C for 2 hours and weighed.
- the gel fraction was calculated from the initial weight and the residual weight according to the following equation.
- Each of the above surface protective films was cut into 25 mm ⁇ 150 mm, attached to a polarizing plate (triacetyl cellulose surface), and allowed to stand at room temperature for 24 hours. Thereafter, the sheet was pulled in a direction of 180 ° (reverse method) at a peeling speed of 300 mm / min and 2000 mm / min, and the force for starting peeling was defined as the peeling force.
- the pressure-sensitive adhesives for surface protection films of Examples I to III were excellent in all of the low-speed peeling property, the high-speed peeling property, the pot life and the stainability. Industrial applicability
- the pressure-sensitive adhesive for a surface protective film of the present invention has good high-speed peelability, Due to a small change in the peeling force due to this, the adherend is not contaminated, and it has properties such as good pot life, it can be widely applied to optical films and the like.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Adhesive Tapes (AREA)
Abstract
Description
Claims
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1020057023507A KR101095383B1 (ko) | 2003-06-30 | 2004-05-10 | 표면 보호 필름용 점착제 및 표면 보호 필름 |
| US10/562,907 US20060177651A1 (en) | 2003-06-30 | 2004-05-10 | Pressure-sensitive adhesive for surface-protective film and surface-protective film |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2003-187775 | 2003-06-30 | ||
| JP2003187775A JP4686960B2 (ja) | 2003-06-30 | 2003-06-30 | 表面保護フィルム用粘着剤および表面保護フィルム |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2005000989A1 true WO2005000989A1 (ja) | 2005-01-06 |
Family
ID=33549733
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2004/006580 Ceased WO2005000989A1 (ja) | 2003-06-30 | 2004-05-10 | 表面保護フィルム用粘着剤および表面保護フィルム |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20060177651A1 (ja) |
| JP (1) | JP4686960B2 (ja) |
| KR (1) | KR101095383B1 (ja) |
| CN (1) | CN100362069C (ja) |
| TW (1) | TW200504169A (ja) |
| WO (1) | WO2005000989A1 (ja) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102660206A (zh) * | 2012-04-09 | 2012-09-12 | 番禺南沙殷田化工有限公司 | 一种光学透明粘合剂组合物及其制备方法 |
| CN103173164A (zh) * | 2011-12-22 | 2013-06-26 | 第一毛织株式会社 | 用于偏光板的粘合剂组合物、偏光板和光学显示器 |
| JPWO2015098314A1 (ja) * | 2013-12-24 | 2017-03-23 | 綜研化学株式会社 | 粘着剤用組成物、粘着剤および粘着シート |
Families Citing this family (51)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4562070B2 (ja) * | 2004-05-14 | 2010-10-13 | 日東電工株式会社 | 粘着剤組成物、粘着シート類、および表面保護フィルム |
| JP2006022313A (ja) * | 2004-06-11 | 2006-01-26 | Toyo Ink Mfg Co Ltd | 粘着剤組成物及びこれを用いた粘着シート |
| JP4705768B2 (ja) * | 2004-08-23 | 2011-06-22 | リンテック株式会社 | 偏光フイルム用感圧接着剤組成物 |
| KR100838973B1 (ko) * | 2005-06-08 | 2008-06-17 | 주식회사 엘지화학 | 아크릴계 점착제 조성물 |
| US7799853B2 (en) * | 2005-09-05 | 2010-09-21 | Nitto Denko Corporation | Adhesive composition, adhesive sheet, and surface protective film |
| KR100813388B1 (ko) | 2005-11-24 | 2008-03-12 | 주식회사 엘지화학 | 아크릴계 점착제 조성물 |
| JP5196894B2 (ja) * | 2006-07-18 | 2013-05-15 | 日本合成化学工業株式会社 | 樹脂組成物、一時表面保護用粘着剤、粘着シート、及び粘着シートの使用方法、並びに粘着シートの製造方法 |
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- 2004-05-10 US US10/562,907 patent/US20060177651A1/en not_active Abandoned
- 2004-05-10 KR KR1020057023507A patent/KR101095383B1/ko not_active Expired - Fee Related
- 2004-05-10 CN CNB2004800185248A patent/CN100362069C/zh not_active Expired - Lifetime
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| CN103173164A (zh) * | 2011-12-22 | 2013-06-26 | 第一毛织株式会社 | 用于偏光板的粘合剂组合物、偏光板和光学显示器 |
| CN102660206A (zh) * | 2012-04-09 | 2012-09-12 | 番禺南沙殷田化工有限公司 | 一种光学透明粘合剂组合物及其制备方法 |
| JPWO2015098314A1 (ja) * | 2013-12-24 | 2017-03-23 | 綜研化学株式会社 | 粘着剤用組成物、粘着剤および粘着シート |
Also Published As
| Publication number | Publication date |
|---|---|
| JP4686960B2 (ja) | 2011-05-25 |
| TWI339677B (ja) | 2011-04-01 |
| TW200504169A (en) | 2005-02-01 |
| CN100362069C (zh) | 2008-01-16 |
| KR101095383B1 (ko) | 2011-12-16 |
| JP2005023143A (ja) | 2005-01-27 |
| US20060177651A1 (en) | 2006-08-10 |
| KR20060018883A (ko) | 2006-03-02 |
| CN1816603A (zh) | 2006-08-09 |
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