TW201800234A - Surface-protective film and optical component attached with the same - Google Patents

Abstract

The present invention provides a surface-protective film and an optical component of using the same. The surface-protective film can be used for an optical film with a non-planar surface. Also, the surface-protective film causes less contamination to the adherend, which does not change over time. Further, the surface-protective film has excellent antistatic performance upon peeling which does not degrade over time. The surface-protective film (10) is formed by applying a release film (5) with a release agent layer (4) on an adhesive layer (2). The release film (5) is formed by laminating the release agent layer (4) on one side of a resin film (3). The release agent layer (4) includes: a release agent with dimethyl polysiloxane as the main component, an antistatic agent which does not react with the release agent, and an ester plasticizer containing at least one ether bond. The antistatic agent is an ionic compound with a melting point of 30~80 DEG C. The antistatic agent and the ester plasticizer are transferred from the release agent layer (4) of the release film (5) to the surface of the adhesive layer (2), thereby reducing the electrostatic voltage when the adhesive layer (2) is peeled off from the adherend.

Description

Surface protection film and optical component with the film

The present invention relates to a surface protection film bonded to the surface of an optical member (hereinafter, also referred to as an optical film) such as a polarizer, a retardation plate, and a lens film for a display. More specifically, a surface protection film with less contamination of adherends is provided, and further, a surface protection film having excellent anti-peel static performance without deterioration over time, and an optical component using the surface protection film are provided. .

Conventionally, optical films such as polarizing plates, retardation plates, lens films for displays, anti-reflection films, hard coating films, transparent conductive films for touch panels, and optical devices such as displays using these films have been manufactured and transported. When a product is used, a surface protection film is bonded to the surface of the optical film, which can prevent surface dirt or scratches in subsequent processes. The appearance inspection of an optical film as an optical product may be performed directly in a state where the surface protective film is bonded to the optical film in order to save the time of peeling the surface protective film and re-adhere, and to improve work efficiency.

Generally, in the manufacturing process of optical products, in order to prevent the adhesion of scars or dirt, a surface protection agent having an adhesive layer on one side of a substrate film is used. Protective film. The surface protection film is bonded to the optical film through a micro-adhesive adhesive layer. The reason why the adhesive layer is made slightly adhesive is that when the used surface protective film is peeled off from the surface of the optical film, it can be easily peeled off, and the adhesive is not adhered and remained (that is, the generation of residual adhesive is prevented) On an optical film as a product to be adhered.

In recent years, in the production process of a liquid crystal display panel, although the number of pieces produced is small, the peeling static voltage generated when the surface protective film bonded to the optical film is peeled off and removed, which causes control for A phenomenon in which circuit components such as a driver IC of a display screen of a liquid crystal display panel are damaged or the orientation of liquid crystal molecules is damaged.

In addition, in order to reduce the power consumption of the liquid crystal display panel, the driving voltage of the liquid crystal material is reduced, and with this, the breakdown voltage of the driving IC is also reduced. Recently, it is required to make the peeling static voltage within the range of + 0.7kV to -0.7kV.

In addition, in recent years, with the spread of 3D displays (stereoscopic displays), FPR (Film Patterned Retarder) films may be laminated on the surface of optical films such as polarizing plates. After peeling off the surface protection film bonded to the surface of an optical film such as a polarizing plate, the FPR film is bonded. However, if the surface of an optical film such as a polarizer is contaminated with an adhesive or an antistatic agent used in a surface protection film, there is a problem that it is difficult to stick the FPR film. Therefore, it is required that the surface protection film used for this purpose has less contamination of adherends.

In addition, in some liquid crystal panel manufacturers, as a method for evaluating the contamination of adherends by a surface protective film, the following method is adopted: by temporarily peeling the surface protective film bonded to an optical film such as a polarizer, Laminate again in the state, and heat-treat it under the specified conditions, and then peel the sheet A method for protecting a film and observing the surface of an adherend. In this evaluation method, if the surface contamination of the adherend is trace, if there is a difference in the surface contamination of the adherend between the part where the air bubbles are mixed and the part in contact with the adhesive of the surface protective film, then Surface contamination by the sticky substance remains as traces of bubbles (sometimes referred to as bubble penetration). Therefore, as an evaluation method for the contamination of the surface of an adherend, this evaluation method is a very strict evaluation method. In recent years, even if it is a result of determination by such a strict evaluation method, the surface protection film which does not have a problem with respect to the contamination property to the surface of an adherend is requested | required.

When peeling a surface protective film from an optical film as an adherend, in order to prevent the occurrence of an adverse condition caused by a high peeling static voltage, a method has been proposed for suppressing the peeling static voltage to a low level. Surface protective film for adhesive layer of antistatic agent.

For example, Patent Document 1 discloses a surface protection film using an adhesive composed of an alkyltrimethylammonium salt, a hydroxyl-containing acrylic polymer, and a polyisocyanate.

In addition, Patent Document 2 discloses an adhesive composition composed of an ionic liquid and an acrylic polymer having an acid value of 1.0 or less, and an adhesive sheet using the adhesive composition.

In addition, Patent Document 3 discloses an adhesive composition composed of an acrylic polymer, a polyether polyol compound, and an alkali metal salt treated with an anion-adsorbing compound, and a surface protection using the adhesive composition. membrane.

In addition, Patent Document 4 discloses an adhesive composition composed of an ionic liquid, an alkali metal salt, a polymer having a glass transition temperature of 0 ° C or lower, And a surface protection film using the adhesive composition.

In addition, Patent Document 5 discloses an adhesive composition for a surface protective sheet of an optical member composed of a polymer containing a liquid ionic salt, and an adhesive sheet.

[Existing technical literature] [Patent Literature]

[Patent Document 1] Japanese Patent Laid-Open No. 2005-131957

[Patent Document 2] Japanese Patent Laid-Open No. 2005-330464

[Patent Document 3] Japanese Patent Laid-Open No. 2005-314476

[Patent Document 4] Japanese Patent Laid-Open No. 2006-152235

[Patent Document 5] Japanese Patent Laid-Open No. 2008-069261

In the aforementioned Patent Documents 1 to 5, an antistatic agent is added to the inside of the adhesive layer. However, the thicker the thickness of the adhesive layer, or the longer the time elapsed after bonding to the adherend, the antistatic agent is transferred from the adhesive layer to the adherend relative to the adherend with the surface protective film attached. The greater the amount. When the amount of the antistatic agent transferred to the adherend increases, there is a possibility that the appearance quality of the optical film as an adherend is lowered, and the adhesiveness of the FPR film may be lowered when the FPR film is bonded.

In order to reduce the increase of the antistatic agent transferred from the adhesive layer to the adherend over time and reduce the thickness of the adhesive layer, other problems will occur. For example, when used for an optical film having unevenness on the surface such as an anti-glare polarizing plate for anti-glare, there is a problem that the adhesive layer is difficult to trace. Bubbles are mixed with the unevenness of the surface of the optical film, and the adhesive force decreases due to the decrease in the adhesive area between the optical film and the adhesive layer. The surface protective film floats or falls off during use.

Therefore, there is a need for a surface protection film for an optical film that can be bonded to an optical film having unevenness on its surface, has very little contamination of the adherend, and does not increase contamination of the adherend even with time. In addition, there is a need for a surface protection film which can suppress the peeling static voltage when peeling the surface protection film from the adherend to a relatively low level.

The inventors of the present application have conducted intensive research in order to solve these problems.

In order to reduce contamination of the adherend and increase the contamination with time, it is necessary to reduce the amount of the antistatic agent component in the adhesive layer which is presumed to be the cause of contaminating the adherend. However, when the amount of the antistatic agent component in the adhesive layer is reduced, the peeling static voltage when the surface protective film is peeled from the adherend increases. Therefore, a method for suppressing the peeling static voltage when peeling the surface protective film from the adherend to a low level without increasing the absolute amount of the antistatic agent component in the adhesive layer has been studied.

As a result, it was found that by coating and drying an antistatic agent-free adhesive composition, and laminating the adhesive composition, an appropriate amount of the antistatic agent component was provided on the surface of the adhesive layer instead of the substrate. An adhesive composition containing an antistatic agent is coated on one surface of the film and dried to form an adhesive layer, so that the peeling static voltage when peeling the surface protective film from the optical film as an adherend can be suppressed to a low level. This completes the present invention.

The present invention has been made in view of the above circumstances, and an object thereof is to provide Provides an optical film with unevenness on the surface, which can be bonded, has less pollution to adherends, has low pollution to adherends, does not change even with time, and has excellent resistance to deterioration with time. A surface protection film having an electrostatic property and an optical component using the surface protection film.

In order to solve the above technical problems, the inventive concept of the present invention is that after the surface protective film of the present invention is coated with an antistatic agent-free adhesive composition on one surface of the substrate film, dried, and laminated with the adhesive layer, An appropriate amount of an antistatic agent is provided on the surface of the adhesive layer, so that the contamination of the adherend is suppressed to a low level, and the peeling static voltage when peeled from the optical film as an adherend is also suppressed to a low level.

In order to solve the above-mentioned technical problems, the present invention provides a surface protection film formed by forming an adhesive layer on one surface of a base film made of a resin having transparency, and bonding a release agent onto the adhesive layer. The release film is formed by laminating a release agent layer on one surface of a resin film, wherein the release agent layer contains a release agent containing polydimethylsiloxane as a main component. An antistatic agent that does not react with the release agent, and an ester plasticizer containing at least one ether bond, the antistatic agent component is an ionic compound having a melting point of 30 to 80 ° C, and the antistatic agent component And the ester plasticizer is transferred from the release agent layer of the release film to the surface of the adhesive layer, thereby reducing the peeling static voltage when the adhesive layer is peeled from the adherend .

The adhesive layer is preferably formed by crosslinking an adhesive composition containing a (meth) acrylate copolymer and a crosslinking agent.

In addition, when the release film is peeled from the adhesive layer, The peeling force is preferably 0.2 N / 50 mm or less.

The present invention also provides an optical component obtained by bonding the surface protection film.

The surface protection film of the present invention has less pollution to adherends, and the low-contamination property to adherends does not change even with time. In addition, the surface protection film of the present invention can be used even if it is an optical film having unevenness on the surface such as an AG polarizing plate. In addition, according to the present invention, it is possible to provide a surface protective film which can suppress the peeling static voltage generated when peeling from an optical film as an adherend and has excellent anti-peeling electrostatic properties which does not deteriorate over time. And an optical component using the surface protection film.

According to the surface protective film of the present invention, since the surface of the optical film can be accurately protected, it is possible to improve productivity and yield.

1‧‧‧ substrate film

2‧‧‧ Adhesive layer

3‧‧‧ resin film

4‧‧‧ peeling agent layer

5‧‧‧ peeling film

7‧‧‧Antistatic agent and ester plasticizer

8‧‧‧ Adhesive (optical component)

10‧‧‧ surface protective film

11‧‧‧ peel off the surface protection film of the release film

20‧‧‧ Optical component with surface protection film

FIG. 1 is a schematic diagram showing the concept of a surface protective film of the present invention.

FIG. 2 is a cross-sectional view showing a state where the release film is peeled from the surface protection film of the present invention.

3 is a cross-sectional view showing an embodiment of an optical component of the present invention.

Hereinafter, the present invention will be described in detail through embodiments.

FIG. 1 is a schematic diagram showing the concept of a surface protection film of the present invention. This surface protection film 10 has an adhesive layer 2 formed on one surface of a transparent base film 1. The surface of the adhesive layer 2 is bonded to the surface of the resin film 3. The release film 5 of the release agent layer 4.

As the base film 1 used for the surface protection film 10 of the present invention, a base film made of a resin having transparency and flexibility is used. Thereby, the external appearance inspection of an optical component can be performed in the state which bonded the surface protection film to the optical component as an adherend. As a film made of a transparent resin used as the base film 1, polyethylene terephthalate, polyethylene naphthalate, polyethylene isophthalate, and poly Polyester film such as butylene terephthalate. In addition to the polyester film, a film made of another resin may be used as long as it has the required strength and has optical adaptability. The base film 1 may be a non-stretched film, or may be a uniaxially or biaxially stretched film. In addition, the stretching ratio of the stretched film or the axial orientation angle formed by crystallization of the stretched film may be controlled to a specific value.

The thickness of the base film 1 used in the surface protection film 10 of the present invention is not particularly limited, but for example, a thickness of about 12 to 100 μm is preferred, and a thickness of about 20 to 50 μm is easier to handle, so it is more preferable .

In addition, if necessary, an antifouling layer, an antistatic layer, a hard coat layer, or the like for preventing surface dirt can be provided on the surface of the base film 1 opposite to the surface on which the adhesive layer 2 is formed. In addition, the surface of the base film 1 may be subjected to an adhesion treatment such as surface modification by corona discharge and application of an anchor agent.

In addition, as long as the adhesive layer 2 used in the surface protection film 10 of the present invention is adhered to the surface of the adherend, it can be easily peeled off after use, and the adhesive is not easy to contaminate the adherend. Although it is especially limited, in consideration of durability after bonding to an optical film, an acrylic adhesive obtained by crosslinking a (meth) acrylate copolymer is usually used.

Examples of the (meth) acrylate copolymer include a main monomer such as n-butyl acrylate, 2-ethylhexyl acrylate, isooctyl acrylate, and isononyl acrylate, and acrylonitrile, vinyl acetate, and formazan. Comonomers such as methyl acrylate and ethyl acrylate; functional monomers such as acrylic acid, methacrylic acid, hydroxyethyl acrylate, hydroxybutyl acrylate, glycidyl methacrylate, and N-methylolmethacrylamide Is a copolymer obtained by copolymerizing a polyoxyalkylene-containing monomer such as methoxypolyethylene glycol methacrylate. The (meth) acrylic acid ester copolymer, the main monomer and other monomers may be (meth) acrylic acid esters. As the monomer other than the main monomer, it may contain one or two or more kinds except (meth) Monomers other than acrylate. The monomers other than the main monomer may be selected from, but are not particularly limited to, the above-mentioned comonomers, functional monomers, polyoxyalkylene-containing monomers, and the like.

Examples of the curing agent added to the adhesive layer 2 include a cross-linking agent that cross-links the (meth) acrylate copolymer, and examples thereof include isocyanate compounds, epoxy compounds, melamine compounds, and metal chelate compounds. Examples of the thickener include rosin, coumarone-indene, terpene, petroleum, and phenol.

The thickness of the adhesive layer 2 used in the surface protection film 10 of the present invention is not particularly limited, but a thickness of about 5 to 40 μm is preferred, and a thickness of about 10 to 30 μm is more preferred. In addition, since the handleability when peeling the surface protection film from the adherend is excellent, it is preferable that the surface protection film has a micro-adhesive force with a peeling strength (adhesive force) of 0.03 to 0.3N / 25mm to the surface of the adherend.胶 胶剂 层 2。 Adhesive layer 2. In addition, since the handleability when peeling the release film 5 from the surface protection film 10 is excellent, the peel force when peeling the release film 5 from the adhesive layer 2 is preferably 0.2 N / 50 mm or less, and more preferably 0.14 N / 50 mm or less.

The release film 5 used in the surface protection film 10 of the present invention is formed by laminating a release agent layer 4 on one surface of the resin film 3, and the release agent layer 4 contains polydimethylsiloxane as a main component. A release agent, an antistatic agent that does not react with the release agent, and an ester plasticizer containing at least one ether bond. In the release film used in the surface protective film of the present invention, the antistatic agent component is preferably an ionic compound having a melting point of 30 to 80 ° C.

Examples of the resin film 3 include a polyester film, a polyimide film, a polyethylene film, a polypropylene film, and a polyimide film. Polyester films are particularly preferred because they have excellent transparency and low cost. The resin film may be an unstretched film or a uniaxially or biaxially stretched film. The stretching ratio of the stretched film and the orientation angle in the axial direction formed by crystallization of the stretched film can be controlled to specific values.

The thickness of the resin film 3 is not particularly limited, but for example, a thickness of about 12 to 100 μm is preferable, and a thickness of about 16 to 50 μm is easy to handle, so it is more preferable.

In addition, if necessary, the surface of the resin film 3 may be subjected to an adhesion treatment such as surface modification by corona discharge and application of an anchoring agent.

Examples of the release agent comprising polydimethylsiloxane as the main component of the release agent layer 4 include well-known silicone-based release agents such as addition reaction type, condensation reaction type, cation polymerization type, and radical polymerization type. . Examples of commercially available addition-reaction type silicone release agents include KS-776A, KS-847T, KS-779H, KS-837, KS-778, and KS-830 (Shin-Etsu Chemical Industry Co., Ltd. )), SRX-211, SRX-345, SRX-357, SD7333, SD7220, SD7223, LTC-300B, LTC-350G, LTC-310 (manufactured by Dow Corning Toray Co., Ltd.) and the like. Condensation reaction type silicone peels sold on the market Examples of the ionizer product include SRX-290 and SYLOFF-23 (manufactured by Dow Corning Toray Co., Ltd.). Examples of commercially available cationic polymerized silicone release agents include TPR-6501, TPR-6500, UV9300, VU9315, UV9430 (manufactured by Momentive Performance Materials Company), and X62-7622 (Shin-Etsu Chemical Industry ( Shares) manufacturing) etc. The products of free-radical polymerized silicone-based release agents on the market include X62-7205 (manufactured by Shin-Etsu Chemical Industry Co., Ltd.) and the like.

As the antistatic agent constituting the release agent layer 4, it is preferred that dispersibility with respect to a release agent solution containing polydimethylsiloxane as a main component is good and that it does not hinder a composition containing polydimethylsiloxane as a main component. Cured antistatic agent for release agents. In addition, in order to transfer from the release agent layer 4 to the surface of the adhesive layer 2 and impart an antistatic effect to the adhesive layer 2, an antistatic agent that does not react with a release agent containing polydimethylsiloxane as a main component is preferred. An ionic compound having a melting point of 30 to 80 ° C is very suitable as such an antistatic agent.

Examples of the ionic compound having a melting point of 30 to 80 ° C. are ionic compounds having cations and anions. nitrogen cation and phosphonium cation, sulfonium cation cation, the anion is hexafluorophosphate (PF ₆ ^-), thiocyanate (SCN ^-), alkylbenzenesulfonates ^{_{(RC 6 H 4 SO 3 -}} ), , tetrafluoroborate (BF ₄ ^-) or a compound of organic and inorganic anions ^- ₍₄ ClO) perchlorate. An ionic compound having a melting point of 30 to 80 ° C can be obtained by selecting the chain length of the alkyl group, the position and number of the substituents, and the like. The cation is preferably a quaternary nitrogen-containing onium cation, and examples thereof include quaternary pyridine cations such as 1-alkylpyridine (carbon atoms at positions 2 to 6 may or may not have a substituent.), Or 1,3-dioxane Quaternary imidazole cations (such as carbon atoms at positions 2, 4, and 5 may or may not have substituents), quaternary imidazole cations such as tetraalkylammonium, and the like.

The amount of the antistatic agent added to the release agent containing polydimethylsiloxane as a main component varies depending on the type of the antistatic agent or the affinity with the release agent. The amount of the antistatic agent to be added can be set in consideration of the peeling static voltage expected when the surface protective film is peeled from the adherend, the contamination property to the adherend, and the adhesive characteristics.

An ester plasticizer containing at least one or more ether bonds constituting the release agent layer 4 is used to improve the antistatic performance of the surface of the adhesive layer 2. As the plasticizer contained in the release agent layer 4, a plasticizer having good dispersibility to a release agent solution containing polydimethylsiloxane as a main component is preferred. In addition, a plasticizer that does not hinder the curing of a release agent containing polydimethylsiloxane as a main component is preferred. In addition, the plasticizer plays a role in assisting the transfer of the antistatic agent contained in the release agent layer 4 from the release agent layer 4 to the surface of the adhesive layer 2. Therefore, the plasticizer is preferably a substance that does not react with a release agent containing polydimethylsiloxane as a main component. As such a plasticizer, an ester plasticizer which contains at least one or more ether bond in a molecule | numerator is suitable.

In the ester plasticizer, at least one ether bond existing in the molecule is required in order to improve the affinity with the antistatic agent. In addition, in the surface protective film of the present invention, a plasticizer is used in order to efficiently transfer the antistatic component from the release agent layer to the surface of the adhesive layer when the release agent layer is in contact with the adhesive layer. . In the present invention, in order to improve the affinity between the release agent layer and the adhesive layer, a plasticizer containing an ester group is preferably used.

Plasticized as esters containing at least one ether bond in the molecule Examples of the agent include diethylene glycol di-2-ethylhexanoate, tetraethylene glycol di-2-ethylhexanoate, hexaethylene glycol di-2-ethylhexanoate, and triethyl Diethylene glycol diethyl butyrate, polyethylene glycol diethyl butyrate, polypropylene glycol diethylhexanoate, triethylene glycol dibenzoate, tetraethylene glycol dibenzoate, poly Ethylene glycol dibenzoate, polypropylene glycol dibenzoate, or polyethylene glycol-2-ethylhexanoate benzoate, and the like. These ester plasticizers can be used alone or in combination of two or more. Here, ethylhexanoate is also referred to as ethylhexanoate, ethylhexoate, ethyl hexane acid ester, and the like. Benzoate refers to benzoate.

The amount of the ester plasticizer added to the release agent containing polydimethylsiloxane as the main component varies depending on the type of the plasticizer and the affinity between the release agent and the release agent. The desired peeling static voltage, the contamination property to the adherend, the adhesion characteristics, and the like are set when the surface protective film is peeled off.

There is no particular limitation on the method for mixing the release agent containing polydimethylsiloxane as the main component, the antistatic agent, and the ester plasticizer. Any of the following methods can be used: a method of adding and mixing an antistatic agent and an ester plasticizer to a release agent containing polydimethylsiloxane as a main component, and then adding and mixing a catalyst for curing the release agent; using an organic A method of adding a polydimethylsiloxane-based release agent as a main component by diluting a solvent in advance, and adding and mixing an antistatic agent, an ester plasticizer, and a curing agent for the release agent; The main component release agent is diluted in an organic solvent in advance, and a catalyst is added and mixed, and then an antistatic agent and an ester plasticizer are added and mixed. In addition, if necessary, an adhesion improving agent such as a silane coupling agent, or a material which assists an antistatic effect such as a polyoxyalkylene-containing compound may be added.

The mixing ratio of the polydimethylsiloxane-based release agent to the antistatic agent and the ester plasticizer is not particularly limited, but it is relative to that of the polydimethylsiloxane-based release agent. The solid content is 100 parts, and the total of the antistatic agent and the ester plasticizer based on the solid content is preferably a ratio of about 5 to 100 parts. When the total amount of the antistatic agent and the ester plasticizer is converted to a solid content of less than 5 parts with respect to 100 parts of the solid content of the release agent containing polydimethylsiloxane as a main component, then The transfer amount of the antistatic agent and the ester plasticizer to the surface of the adhesive layer is reduced, and it is difficult to exert the antistatic function imparted to the adhesive. In addition, when the total amount of the antistatic agent and the ester plasticizer is converted into a solid content of more than 100 parts with respect to 100 parts of the solid content of the release agent containing polydimethylsiloxane as a main component, , The antistatic agent, the ester plasticizer and the polydimethylsiloxane-based release agent are also transferred to the surface of the adhesive layer at the same time, so the adhesive characteristics of the adhesive may be reduced.

The method of forming the adhesive layer 2 on the base film 1 of the surface protection film 10 of the present invention and the method of bonding the release film 5 can be performed by a known method, and are not particularly limited. Specifically, the following methods can be enumerated: (1) Applying the resin composition for forming the adhesive layer 2 on one surface of the base film 1 and drying it to form an adhesive layer, and then bonding the release film 5 Method; (2) A method of applying the resin composition for forming the adhesive layer 2 on the surface of the release film 5 and drying it, and forming the adhesive layer, followed by a method of bonding the base film 1 and the like, using any of them Any method.

The method of forming the adhesive layer 2 on the surface of the base film 1 may be a known method. Specifically, reverse coating, doctor blade coating, gravure coating, sandwich extrusion coating, Meyer bar coating, and air knife coating can be used. A known coating method such as cloth.

In addition, similarly, the release agent layer 4 may be formed on the resin film 3 and may be performed by a known method. Specifically, known coating methods such as gravure coating, Meyer bar coating, and air knife coating can be used.

The surface potential of the surface protective film 10 of the present invention having the above structure when the adhesive layer is peeled from the optical film as an adherend is preferably +0.7 kV to -0.7 kV. Furthermore, the surface potential is more preferably +0.5 kV to -0.5 kV, and particularly preferably +0.1 kV to -0.1 kV. This surface potential can be adjusted by adding or subtracting the types and addition amounts of the antistatic agent and the ester plasticizer contained in the release agent layer.

FIG. 2 is a cross-sectional view showing a state after the release film is peeled from the surface protection film of the present invention.

By peeling the release film 5 from the surface protection film 10 shown in FIG. 1, a part of the antistatic agent and the ester plasticizer (reference numeral 7) contained in the release agent layer 4 of the release film 5 is transferred. It is printed (attached) to the surface of the adhesive layer 2 of the surface protection film 10. Therefore, in FIG. 2, the antistatic agent and the ester-based plasticizer transferred on the surface of the adhesive layer 2 of the surface protective film 11 in a state where the release film is peeled off are indicated by spots of reference numeral 7. By transferring the component 7 of the antistatic agent and the ester plasticizer from the release film 5 to the surface of the adhesive layer 2, the adhesive layer 2 is removed from the adherend compared to the adhesive layer 2 before the transfer. The peeling static voltage during peeling is reduced. The peeling static voltage when the adhesive layer is peeled from the adherend can be measured by a known method. For example, after the surface protective film is adhered to an adherend such as a polarizing plate, the surface protective film is peeled at a peeling speed of 40 m per minute using a high-speed peel tester (manufactured by TESTER SANGYO CO, .LTD.) While using a surface potential The meter (manufactured by KEYENCE CORPORATION) measures the surface potential of the surface of the adherend every 10 ms, and uses the maximum value of the absolute value of the surface potential at this time as the peeling static voltage (kV).

In the surface protection film of the present invention, when the surface protection film 11 in a state where the release film is peeled off as shown in FIG. 2 is bonded to the adherend, the antistatic transferred onto the surface of the adhesive layer 2 Agents and ester plasticizers are in contact with the surface of the adherend. Thereby, the peeling static voltage at the time of peeling the surface protection film from an adherend again can be suppressed low.

FIG. 3 is a cross-sectional view showing an embodiment of an optical component of the present invention.

The release film 5 is peeled from the surface protection film 10 of the present invention to expose the pressure-sensitive adhesive layer 2, and is bonded to the optical member 8 as an adherend via the pressure-sensitive adhesive layer 2.

That is, FIG. 3 shows an optical member 20 to which the surface protective film 11 of the present invention is bonded. Examples of the optical component include optical films such as a polarizer, a retardation plate, a lens film, a polarizer that also functions as a retardation plate, and a polarizer that also functions as a lens film. The above-mentioned optical component can be used as a component of a liquid crystal display device such as a liquid crystal display panel, an optical system device of various measuring instruments, and the like. In addition, examples of the optical component include an optical film such as an antireflection film, a hard coat film, and a transparent conductive film used for a touch panel.

According to the optical member of the present invention, when the surface protective film 11 is peeled off from the optical member (optical film) as an adherend, the peeling static voltage can be sufficiently reduced. Therefore, there is no need to worry about damaging circuit components such as a driving IC, a TFT element, and a gate line driving circuit, and it is possible to improve production efficiency in a manufacturing process such as a liquid crystal display panel and maintain reliability in the manufacturing process.

[Example]

Next, the present invention will be further described based on examples.

(Example 1) (Production of surface protective film)

5 parts by weight of an addition reaction type silicone (manufactured by Dow Corning Toray Co., Ltd., trade name: SRX-345), 0.75 parts by weight of N-butyl-4 as an ionic compound having a melting point of 48 ° C -Methylpyridine hexafluorophosphate, 0.75 parts by weight of tetraethylene glycol di-2-ethylhexanoate, 95 parts by weight of a mixed solvent of toluene and ethyl acetate of 1: 1, and 0.05 parts by weight of a platinum catalyst (Manufactured by Dow Corning Toray Co., Ltd., trade name: SRX-212) was mixed and stirred to prepare a coating material for forming the release agent layer of Example 1. On the surface of the polyethylene terephthalate film having a thickness of 38 μm, a coating for forming the release agent layer of Example 1 was applied using a Mayer bar to a thickness of 0.2 μm after drying. The hot-air loop oven was dried for 1 minute to obtain the release film of Example 1. On the other hand, it was copolymerized with 90 parts by weight of 2-ethylhexyl acrylate, 7 parts by weight of methoxypolyethylene glycol (400) methacrylate, and 3 parts by weight of 2-hydroxyethyl acrylate. 100 parts by weight of a 30% ethyl acetate solution of an adhesive polymer composed of a polymer, and 1.2 parts by weight of an isocyanate curing agent (manufactured by TOSOH CORPORATION, trade name: CORONATE (registered trademark) HX) was mixed and mixed, and Preparation Example 1 Adhesive composition. In addition, CORONATE (registered trademark) HX is a curing agent of HDI type (hexamethylene diisocyanate type).

The adhesive composition of Example 1 was applied to the surface of a polyethylene terephthalate film having a thickness of 38 μm so that the thickness after drying was 20 μm, and then dried using a 100 ° C. hot-air loop oven. For 2 minutes, an adhesive layer was formed. Of Then, on the surface of this adhesive layer, the release film of Example 1 prepared above was bonded via a release agent layer (silicone-treated surface). The obtained adhesive film was held in an environment at 40 ° C. for 5 days to cure the adhesive layer to obtain the surface protective film of Example 1.

(Example 2)

Except that instead of N-butyl-4-methylpyridine hexafluorophosphate, 1-methyl-3-ethylimidazole hexafluorophosphate was used as an ionic compound having a melting point of 62 ° C., as in Example 1. Thus, a surface protection film of Example 2 was obtained.

(Comparative example 1)

5 parts by weight of an addition reaction type silicone (manufactured by Dow Corning Toray Co., Ltd., trade name: SRX-345), 95 parts by weight of a mixed solvent of toluene and ethyl acetate of 1: 1, and 0.05 parts by weight A platinum catalyst (manufactured by Dow Corning Toray Co., Ltd., trade name: SRX-212) was mixed and mixed by stirring to prepare a coating material for forming a release agent layer of Comparative Example 1. On the surface of the polyethylene terephthalate film having a thickness of 38 μm, a coating material for forming the release agent layer of Comparative Example 1 was applied with a Meyer bar to a thickness of 0.2 μm after drying, and used. A 120 degreeC hot-air loop oven was dried for 1 minute, and the peeling film of the comparative example 1 was obtained. On the other hand, with respect to 100 parts by weight of the adhesive polymer solution (solid content: 30% ethyl acetate solution) of Example 1, 0.3 parts by weight of N-butyl-4-methylpyridine was stirred and mixed. Fluorophosphate, 1.5 parts by weight of an isocyanate-based curing agent (manufactured by Dow Corning Toray Co., Ltd., trade name: Coronate (registered trademark) HX), an adhesive composition of Comparative Example 1 was prepared.

The adhesive composition of Comparative Example 1 was applied to the surface of a polyethylene terephthalate film having a thickness of 38 μm so that the thickness after drying was 20 μm, and then performed using a 100 ° C. hot-air loop drying oven. Dry for 2 minutes to form an adhesive layer. Then, the release agent layer (silicone-treated surface) of the release film of the comparative example 1 prepared above was stuck on the surface of this adhesive layer. The obtained adhesive film was kept at 40 ° C for 5 days to cure the adhesive layer to obtain a surface protection film of Comparative Example 1.

(Comparative example 2)

A surface protection film of Comparative Example 2 was obtained in the same manner as in Comparative Example 1 except that N-butyl-4-methylpyridine hexafluorophosphate was not added to the adhesive layer.

(Comparative example 3)

A surface protection film of Comparative Example 3 was obtained in the same manner as in Example 1 except that tetraethylene glycol di-2-ethylhexanoate, which was an ester-based plasticizer, was not added to the release agent layer.

(Example 3)

A surface protection film of Example 3 was obtained in the same manner as in Example 1 except that the following adhesive composition was used in place of the adhesive composition of Example 1. The adhesive composition contained 100 parts by weight of A 30% ethyl acetate solution of an adhesive polymer composed of 58 parts by weight of 2-ethylhexyl acrylate, 38 parts by weight of butyl acrylate, and 4 parts by weight of copolymer of 2-hydroxyethyl acrylate, added 1.2 parts by weight of an isocyanate-based curing agent (manufactured by TOSOH CORPORATION, trade name: Coronate (registered trademark) HX) was mixed.

(Example 4)

A surface protection film of Example 4 was obtained in the same manner as in Example 1 except that the following adhesive composition was used instead of the adhesive composition of Example 1. The adhesive composition was 100 parts by weight based on 100 parts by weight of A 30% ethyl acetate solution of an adhesive polymer composed of 96 parts by weight of 2-ethylhexyl acrylate and 4 parts by weight of 2-hydroxyethyl acrylate copolymer, and 1.2 parts by weight of isocyanate was added and mixed Curing agent (manufactured by TOSOH CORPORATION, trade name: Coronate (Registered trademark) HX).

The methods and results of the evaluation tests are shown below.

<Method for measuring peeling force of release film>

A sample of the surface protective film was cut into a width of 50 mm and a length of 150 mm. In a test environment of 23 ° C. × 50% RH, a tensile tester was used to measure the strength of the peeling film at a peeling speed of 300 mm / min in a direction of 180 °, and this was used as the peeling force of the peeling film (N / 50mm ).

<Method for measuring adhesion of surface protective film>

An anti-glare low-reflection polarizer (AG-LR polarizer) was bonded to the surface of a glass plate with a double-sided adhesive tape using a laminator. Then, a surface protection film cut to a width of 25 mm was attached to the surface of the polarizer, and then stored in a test environment at 23 ° C. × 50% RH for one day. Thereafter, the tensile strength was measured at a peeling speed of 300 mm / minute in a direction of 180 °, and the strength was measured as the adhesive force (N / 25 mm).

<Method for measuring peeling static voltage of surface protective film>

An anti-glare low-reflection polarizer (AG-LR polarizer) was bonded to the surface of a glass plate with a double-sided adhesive tape using a laminator. Then, a surface protection film cut to a width of 25 mm was attached to the surface of the polarizer, and then stored in a test environment at 23 ° C. × 50% RH for one day. Thereafter, the surface protective film was peeled at a peeling speed of 40 m per minute using a high-speed peel tester (manufactured by TESTER SANGYO CO, LTD.), And the surface potential of the surface of the polarizer was measured every 10 ms using a surface potentiometer (manufactured by KEYENCE CORPORATION), The maximum value of the absolute value of the surface potential at this time was taken as the peeling static voltage (kV).

<A method for determining the surface contamination of a surface protective film>

An anti-glare low-reflection polarizer (AG-LR polarizer) was bonded to the surface of a glass plate with a double-sided adhesive tape using a laminator. Then, a surface protective film cut to a width of 25 mm was attached to the surface of the polarizer, and then stored in a test environment at 23 ° C. × 50% RH for 3 days and 30 days. After that, the surface protective film was peeled off, and visually observed whether there was contamination on the surface of the polarizer. As a criterion for determining the surface contamination property, a case where no pollution was transferred on the polarizing plate was evaluated as ()), and a case where transfer was confirmed to be contaminated on the polarizer was evaluated as (×).

The measurement results of the obtained surface protective films of Examples 1 to 4 and Comparative Examples 1 to 3 are shown in Tables 1 to 2. "2EHA" is 2-ethylhexyl acrylate, "HEA" is 2-hydroxyethyl acrylate, "BA" is butyl acrylate, and "# 400G" is methoxypolyethylene glycol (400) methacrylate "AS-a" is N-butyl-4-methylpyridine hexafluorophosphate, "AS-b" is 1-methyl-3-ethylimidazole hexafluorophosphate, and "plasticizer" is tetra Ethylene glycol di-2-ethylhexanoate. In Tables 1 and 2, the composition of the adhesive layer is expressed in parts by weight so that the total amount of the adhesive polymer (solid content) is about 100 parts by weight. Therefore, in the adhesive layer of Comparative Example 1, the weight ratio of the adhesive polymer (solid content) to N-butyl-4-methylpyridine hexafluorophosphate is 30 parts by weight: 0.3 parts by weight = 100 parts by weight : 1.0 part by weight.

From the measurement results shown in Tables 1 and 2, the following conclusions can be obtained.

The surface protection films of Examples 1 to 4 of the present invention have moderate adhesion, have no pollution to the surface of the adherend, and have a low peeling static voltage when the surface protective film is peeled from the adherend.

On the other hand, the surface of Comparative Example 1 containing an antistatic agent in the adhesive layer The protective film has a low peeling static voltage when the surface protective film is peeled off from the adherend, but the contamination of the adherend increases after peeling.

In addition, in the surface protection film of Comparative Example 2 which did not contain an antistatic agent in both the adhesive layer of the surface protection film and the release agent layer of the release film, the surface protection film had good contamination to adherends, but protected the surface. When the film is peeled from the adherend, the peeling static voltage increases.

That is, the surface protective film of Comparative Example 1 containing an antistatic agent in the adhesive layer of the surface protective film, and the comparative example of not including the antistatic agent in the adhesive layer of the surface protective film and the release agent layer of the release film. In the surface protection film of 2, it is difficult to achieve both reduction in peeling static voltage and contamination of adherends.

On the other hand, after the antistatic agent and the ester plasticizer are contained in the release agent layer of the release film, the antistatic agent and the ester plasticizer having the release agent layer transferred only on the surface of the adhesive layer In the surface protective films of Examples 1 to 4, since a small amount of an ester plasticizer was added, the peeling static voltage was significantly reduced, so there was no contamination of the adherend, and the anti-peeling electrostatic performance was also good.

In addition, the surface protective film of Comparative Example 3, which contained only the antistatic agent and no ester plasticizer in the release agent layer, did not contaminate the adherend, and also had good antistatic properties. However, when compared with the surface protection films of Examples 1 to 4 containing an antistatic agent and an ester plasticizer in the release agent layer, the peeling static voltage increased.

[Industrial use possibilities]

The surface protective film of the present invention can be used to protect the surface by bonding the optical member and the like in the production process of optical films such as polarizers, retardation plates, and lens films, and various other optical members. In addition, the surface protective film of the present invention can reduce the static voltage generated when it is peeled from the adherend. It can reduce the time-dependent change of anti-peel static electricity performance and the contamination of adherends, can improve the yield of the production process, and has a large industrial use value.

1‧‧‧ substrate film

2‧‧‧ Adhesive layer

3‧‧‧ resin film

4‧‧‧ peeling agent layer

5‧‧‧ peeling film

7‧‧‧Antistatic agent and ester plasticizer

10‧‧‧ surface protective film

Claims (4)

A surface protection film is formed by forming an adhesive layer on one surface of a base film made of a resin having transparency, and bonding a release film having a release agent layer on the adhesive layer. It is characterized in that the release film is formed by laminating the release agent layer on one side of a resin film, wherein the release agent layer contains a release agent containing polydimethylsiloxane as a main component, and An antistatic agent reacted by the release agent, and an ester plasticizer containing at least one ether bond. The antistatic agent component is an ionic compound having a melting point of 30 to 80 ° C. The antistatic agent component and the ester A plasticizer is transferred from the release agent layer of the release film to the surface of the adhesive layer, and reduces the peeling static voltage when the adhesive layer is peeled from the adherend. The surface protection film according to item 1 of the scope of application for a patent, wherein the adhesive layer is formed by crosslinking an adhesive composition containing a (meth) acrylate copolymer and a crosslinking agent. The surface protective film according to item 1 or 2 of the scope of application for a patent, wherein a peeling force when the peeling film is peeled from the adhesive layer is 0.2 N / 50 mm or less. An optical component is formed by laminating a surface protection film according to any one of claims 1 to 3 of an applied patent scope.