Patent Application
20140329083
The present invention relates to an adhesive film for a touch panel and a touch panel.
Recently, the market for mobile communication devices, such as mobile phones, PHSs, and PDAs, has been growing. Such mobile communication devices are moving towards slimness, lightweight, low-power consumption, high resolution, and high brightness.
In particular, a device equipped with a touch panel or touchscreen as an input unit has a structure in which a transparent conductive plastic film, for example, a polyethylene terephthalate (PET) base film having a conductive thin layer of indium tin oxide (ITO) formed on one side thereof, is stacked on a conductive glass, a reinforcing material, or a decorative film through an adhesive film in consideration of weight reduction and breakage prevention.
An adhesive for attaching a transparent conductive film in a touchscreen or touch panel needs to have various physical properties, such as surface leveling performance for relieving an uneven surface due to a decorative film, durability for suppressing generation of curls or bubbles when exposed to severe conditions, e.g., high temperature or high humidity, cuttability for preventing the adhesive from sticking out or from being squashed when cut, and excellent adhesion to various substrates, as well as optical characteristics and workability.
Particularly, in manufacture of a touch panel or touchscreen, a process of curing an adhesive composition is performed at 140° C. or more for 2 hours or more. Also, a process of bonding an anisotropic conductive foil (ACF) in assembly of a printed circuit board (PCB) is performed at a high temperature of about 120° C. or more. In these processes, an adhesive composition or adhesive having low heat resistance can cause air pockets, bubbles, separation, or curls between the adhesive and an adherend (e.g., a transparent conductive film).
Further, when writing on a surface of a window of a touch panel, inadequate durability of an adhesive film disposed under the window can cause separation of the adhesive. Further, low restoring force by low elasticity causes a trace to remain after writing.
Korean Patent Publication No. 2006-0043847 discloses an adhesive composition, which is a transparent adhesive used for a touch panel, and includes an acrylic polymer having a weight average molecular weight of 500,000 to 900,000 and a low molecular weight oligomer having a weight average molecular weight of 3,000 to 6,000.
However, the adhesive disclosed in this publication generates air pockets or bubbles between the adhesive and an adherend, or causes panel warping, separation, or curling due to considerably low heat resistance when applied to a high-temperature process at about 100° C. or more. Further, when writing on a surface of a window of a touch panel, a trace can remain after writing due to reduced restoring force by low molecular weight additives included in the adhesive, and separation of the adhesive can occur over time.
The present invention provides an adhesive film for a touch panel and a touch panel.
One aspect of the present invention provides an adhesive film for a touch panel including a sheet-form adhesive layer and satisfying Equation 1:
X≧100,000
where X represents the number of times the adhesive film passes through a writing test performed using a 0.8R pen at a transfer rate of 60 mm/s and a weight of 450 gf until an average terminal resistance increase value of the touch panel is 1Ω or more.
Another aspect of the present invention provides a touch panel, which includes a window film; the adhesive film according to the present invention attached to a lower surface of the window film; and a conductive laminate attached to a lower surface of the adhesive film.
According to the present invention, an adhesive film has excellent heat resistance in high-temperature processes in manufacture of a touch panel, such as a curing process or a PCB assembly process. In addition, the adhesive film exhibits superior wettability to adherends, optical characteristics, cuttability, workability, and durability and does not cause panel warpage, separation, and curling.
The present invention relates to an adhesive film for a touch panel which includes a sheet-form adhesive layer and satisfies the following Equation 1:
X≧100,000,
where X represents the number of times the adhesive film passes through a writing test performed using a 0.8R pen at a transfer rate of 60 mm/s and a weight of 450 gf until an average terminal resistance increase value of the touch panel is 1Ω or more.
Hereinafter, the adhesive film according to the present invention will be described in detail.
According to the present invention, the adhesive film includes a sheet-form adhesive layer and the number of times the adhesive film normally subjected to a writing test conducted under specific conditions satisfies Equation 1.
In the present invention, the writing test may be conducted as follows.
Writing test is conducted using a resistive touch panel prepared using a double-sided adhesive sheet, which is obtained by forming sheet-form adhesive layers included in the adhesive film of the present invention on opposite sides of a substrate. In this case, the substrate for the double-sided adhesive sheet is a polyethylene terephthalate (PET) film having a thickness of 12 μm, and the sheet-form adhesive layers formed on the opposite sides of the substrate have a thickness of 50 μm.
<Configuration of the Sample>
Window film 11: PET film having a thickness of 1,885 μm
Conductive plastic films 13 and 14: PET film including an indium tin oxide (ITO) layer 13b, 14b formed on one surface thereof and having a thickness of 125 μm (manufactured by Hansung)
DAT 15: Acrylic adhesive having a thickness of 80 μm (FD8085, manufactured by LG Hausys)
Adhesive film 17: Acrylic adhesive having a thickness of 50 μm (OA9052T, manufactured by LG Hausys)
Plastic substrate 18: Polycarbonate substrate having a thickness of 1 mm (manufactured by I-Component)
In the present invention, the sample 10 of
X
3
=R
2
−R
1,
where X3 represents an average terminal resistance increase value of the touch panel, R1 represents an average terminal resistance of the touch panel before writing test, and R2 represents an average terminal resistance of the touch panel after writing test.
The adhesive film has a writing test passing time of 100,000 or more, preferably 120,000 or more, and more preferably 150,000 or more. Within this range, the adhesive film may exhibit superior durability when applied to a touch panel.
In the present invention, an upper limit of the writing test passing time is not particularly limited. That is, the greater the writing test passing time, the more durability the adhesive film exhibits. In one embodiment, the adhesive film has a writing test passing time of, for example 700,000 or less, preferably 500,000 or less, and more preferably 300,000 or less.
The adhesive film may further include a base film. In this case, the sheet-form adhesive layer may be directly attached to opposite sides of the base film.
The adhesive film according to the present invention may be used to bond a window film and a conductive laminate in a resistive touch panel. However, a conventional adhesive film 30 for a touch panel used for this purpose generally has a structure in which a hard coating 31 is formed between a substrate 12b and an adhesive layer 12a to secure surface pressure durability, as shown in
However, the adhesive film according to the present invention satisfies Equation 1 and thus may secure excellent surface pressure durability without a hard coating, as shown in
There is no particular restriction as to the kind of the base film included in the adhesive film of the present invention, and any plastic film commonly used in the art may be used. Examples of the base film may include a PET film, a polytetrafluoroethylene film, a polyethylene film, a polypropylene film, a polybutene film, a polybutadiene film, a vinyl chloride copolymer film, a polyurethane film, an ethylene-vinyl acetate film, an ethylene-propylene copolymer film, an ethylene-ethyl acetate copolymer film, an ethylene-methyl acetate copolymer film, or a polyimide film. In particular, a PET film may be used, without being limited thereto.
In the present invention, the base film has a thickness of 5 to 100 μm, preferably 10 to 50 μm. Within this range, the adhesive film can not only be applied to a thin touch panel or touchscreen but also has excellent heat resistance, optical characteristics, cuttability, workability, wettability, and durability.
The adhesive layer included in the adhesive film of the present invention may satisfy Equation 2:
X
1≧6 kg/cm2, [Equation 2]
where X1 represents a dynamic shear strength value of the adhesive layer, measured at 140° C. and a crosshead speed of 0.8 mm/sec using a sample prepared by attaching the adhesive layer to the ITO PET film and a glass substrate to be interposed therebetween.
That is, the adhesive layer according to the present invention has dynamic shear strength satisfying Equation 2, as measured by a dynamic shear test under specified conditions. X1 is 6.5 to 15 kg/cm2, preferably 6.5 to 10 kg/cm2.
In the test, the double-sided adhesive sheet has a size of 2.5 cm×2.5 cm (width x length) and a thickness of 112 μm. Here, the base film 12b has a thickness of 12 μm and each adhesive layer 12a attached to the opposite sides of the base film 12b has a thickness of 50 μm. After preparing the sample as shown in
In the present invention, when the dynamic shear strength of the adhesive layer is 6.0 kg/cm2 or more, the adhesive may have excellent wettability to a variety of adherends, optical characteristics, cuttability, workability and durability, particularly superior heat resistance, and thus does not cause warpage, separation, and curling under high-temperature conditions.
The adhesive layer according to the present invention may also satisfy Equation 3:
X
2≧10 min, [Equation 3]
where X2 represents a maintenance time of the adhesive layer, i.e., static shear maintenance time, measured using a sample at 140° C. by applying a load of 2 kg to an ITO PET film. Here, the sample is prepared by attaching the adhesive layer to the ITO PET film and a glass substrate to be interposed therebetween.
As shown in
In the test shown in
After preparing the sample as shown in
According to the present invention, the adhesive layer has a static shear maintenance time (X2) of 10 minutes or more, preferably 15 minutes or more, and more preferably 20 minutes or more. If the static shear maintenance time of the adhesive layer is 10 minutes or more, the adhesive has superior heat resistance and thus does not cause warping, separation, and curling under high-temperature conditions.
In the present invention, an upper limit of the static shear maintenance time is, without being particularly limited to, for example, about 80 minutes or less, preferably 60 minutes or less, and more preferably 50 minutes or less.
The sheet-form adhesive layer according to the present invention may be a cured product of an adhesive composition including an acrylic resin and a polyfunctional crosslinking agent. In this case, the acrylic resin included in the composition may have a weight average molecular weight of 1,000,000 or more. Here, the weight average molecular weight is obtained based on polystyrene conversion in GPC (Gel Permeation Chromatography). If the acrylic resin has a weight average molecular weight of 1,000,000 or more, the adhesive layer can have excellent heat resistance and durability, and does not contaminate an adherend by transferring to the adherend in re-peeling.
In the present invention, an upper limit of the weight average molecular weight of the acrylic resin is 3,000,000 or less, preferably 2,500,000 or less in view of coatability, without being particularly limited thereto.
In the present invention, the acrylic resin may be, for example, a polymer of a monomer mixture including a (meth)acrylic acid ester monomer and a crosslinking monomer.
There is no particular restriction as to the kind of the (meth)acrylic acid ester monomer, which may include, for example, alkyl(meth)acrylates. In this case, when too long an alkyl group is included in the monomer, the cohesion of the cured product may decrease and the glass transition temperature or tack of the cured product may not be properly adjusted. Thus, alkyl(meth)acrylates having a C1 to C14, preferably C1 to C8 alkyl group are used. Examples of such monomers may include methyl(meth)acrylate, ethyl(meth)acrylate, n-propyl(meth)acrylate, isopropyl(meth)acrylate, n-butyl(meth)acrylate, t-butyl(meth)acrylate, sec-butyl(meth)acrylate, pentyl(meth)acrylate, 2-ethylhexyl(meth)acrylate, 2-ethylbutyl(meth)acrylate, n-octyl(meth)acrylate, isooctyl(meth)acrylate, isobornyl(meth)acrylate, or isononyl methacrylate, which may be used alone or as mixtures.
To arrive at the adhesive composition satisfying the condition of equation 1, one skilled in the art may manipulate the kinds of monomers constituting the base resin, the amounts of the monomers therein, and the molecular weight of the base resin. In particular, one non-limiting example for obtaining the composition satisfying the condition of equation 1 is to begin by selecting a hard monomer for the base resin.
A hard monomer is generally is indicated as a monomer having a high glass transition temperature (Tg), above 20° C., whereas a soft monomer is generally indicated as a monomer having a low glass transition temperature (Tg), below −40° C. Typically, hard monomers provide cohesiveness and soft monomers provide for tackiness.
In one non-limiting embodiment, the hard monomer is a (meth)acrylic ester monomer. According to the present subject matter, the (meth)acrylic ester monomer comprises 25 to 100 percent by weight of methyl acrylate.
A base resin including such amounts by weight of the hard monomer should also have a high molecular weight and a narrow distribution of the molecular weight. For example, one non-limiting exemplary way to obtain such a polymer is to introduce initiators in multiple steps.
Further, to satisfy the condition of equation 1, the base resin may have a polymer dispersity index (PDI) of 10 or less, which indicates that the distribution of the molecular weight of the base resin is narrow.
The crosslinking monomer included in the monomer mixture is a monomer including both a copolymerizable functional group (e.g., a, β-unsaturated carbon-carbon double bond) and a crosslinking functional group, and may provide a resin with a crosslinking functional group reacting with the polyfunctional crosslinking agent.
Examples of the crosslinking monomer may include a hydroxyl group containing monomer, a carboxylic group containing monomer, and a nitrogen containing monomer, which may be used alone or as mixtures. In some embodiments, a carboxylic group containing monomer may be advantageously used as the crosslinking monomer, without being limited thereto. Examples of the hydroxyl group containing monomer may include 2-hydroxyethyl(meth)acrylate, 2-hydroxypropyl(meth)acrylate, 4-hydroxybutyl(meth)acrylate, 6-hydroxyhexyl(meth)acrylate, 8-hydroxyoctyl(meth)acrylate, 2-hydroxyethylene glycol(meth)acrylate, or 2-hydroxypropylene glycol(meth)acrylate, without being limited thereto. Examples of the carboxylic group containing monomer may include acrylic acid, methacrylic acid, 2-(meth)acryloyloxy acetic acid, 3-(meth)acryloyloxy propyl acid, 4-(meth)acryloyloxy butyl acid, an acrylic acid dimer, itaconic acid, or maleic acid, without being limited thereto. Examples of the nitrogen containing monomer may include 2-isocyanatoethyl(meth)acrylate, 3-isocyanatopropyl(meth)acrylate, 4-isocyanatobutyl(meth)acrylate, (meth)acryl amide, N-vinylpyrrolidone, or N-vinylcaprolactam, without being limited thereto.
In a non-limiting exemplary embodiment, an adhesive composition satisfying equation 1 is obtained by selecting a hard monomer for the base resin. Particularly, the hard monomer, such as methyl acrylate, has a high glass transition temperature (Tg). Further, the base resin should also have a high molecular weight and narrow distribution of the molecular weight. Generally, it is difficult to make a polymer polymerized from a hard monomer that also has a high molecular weight. However, one exemplary way to obtain such a polymer is to introduce initiators in multiple steps. Additionally, to attain a composition satisfying equation 1, the polymer dispersity index (PDI) of the base resin is controlled to be 10 or less. Controlling the PDI to 10 or below indicates that the distribution of the molecular weight of the base resin is narrow.
In the present invention, the monomer mixture includes 80 to 99.9 parts by weight of the (meth)acrylic acid ester monomer and 0.1 to 20 parts by weight of the crosslinking monomer, preferably 90 to 99.9 parts by weight of the (meth)acrylic acid ester monomer and 0.1 to 20 parts by weight of the crosslinking monomer. Within this range, the adhesive can have excellent reliability, handling properties, durability, and re-peeling properties and can effectively prevent separation or peeling due to decrease in initial adhesive strength.
Unless otherwise indicated in the specification, “parts by weight” denotes “ratio by weight.”
In the present invention, there is no particular restriction as to a method of preparing an acrylic resin by polymerizing the monomer mixture including the foregoing ingredients. For example, a general polymerization method, such as solution polymerization, photo-polymerization, bulk polymerization, suspension polymerization, or emulsion polymerization, may be used.
The adhesive composition according to the present invention further includes the polyfunctional crosslinking agent, and cohesion or adhesion of the cured product may be adjusted based on the amount of the polyfunctional crosslinking agent.
There is no particular restriction as to the kind of the polyfunctional crosslinking agent to be used in the present invention. For example, the polyfunctional crosslinking agent may include common crosslinking agents, such as isocyanate compounds, epoxy compounds, aziridine compounds, and chelating agents. Examples of the isocyanate compound may include tolylene diisocyanate, xylene diisocyanate, diphenylmethane diisocyanate, hexamethylene diisocyanate, isophorone diisocyanate, tetramethylxylene diisocyanate, naphthalene diisocyanate, and adducts of at least one of these isocyanate compounds and a polyol (e.g., trimethylolpropane), which may be used alone or as mixtures. Examples of the epoxy compound may include at least one selected from the group consisting of ethylene glycol diglycidyl ether, triglycidyl ether, trimethylolpropane triglycidyl ether, N,N,N′,N′-tetraglycidyl ethylene diamine, and glycerin diglycidyl ether. Examples of the aziridine compound may include at least one selected from the group consisting of N,N′-toluene-2,4-bis(1-aziridinecarboxamide), N,N′-diphenylmethane-4,4′-bis(1-aziridinecarboxamide), triethylenemelamine, bisisophthaloyl-1-(2-methylaziridine), and tri-1-aziridinylphosphine oxide. Examples of the chelating agent may include compounds obtained by coordinating acetylacetone or ethyl acetoacetate with polyvalent metal, such as aluminum, iron, zinc, tin, titanium, antimony, magnesium, and/or vanadium, without being limited thereto.
The polyfunctional crosslinking agent is present in an amount of 0.01 to 10 parts by weight, preferably 0.01 to 5 parts by weight based on 100 parts by weight of the acrylic resin. If the amount of the crosslinking agent is less than 0.01 parts by weight, cohesion of the cured product may deteriorate, causing bubbles under high-temperature conditions. If the amount of the crosslinking agent is greater than 10 parts by weight, the adhesive is excessively cured, causing decrease in adhesive strength and peel strength. Thus, peeling or separation between layers can occur, reducing durability.
The adhesive composition according to the present invention may further include a silane coupling agent. The coupling agent functions to enhance adhesion and adhesive stability of the cured product to an object, particularly a glass substrate, thus improving heat resistance and moisture resistance. Also, a proper amount of the silane coupling agent may enhance adhesive reliability of the cured product under high-temperature and/or high-humidity conditions and ultimate adhesive strength of the cured product.
There is no particular restriction as to the kind of the silane coupling agent, and examples of the silane coupling agent may include γ-glycidoxypropyltrimethoxysilane, γ-glycidoxypropylmethyldiethoxysilane, γ-glycidoxypropyltriethoxysilane, 3-mercaptopropyltrimethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, γ-methacryloxypropyltrimethoxysilane, γ-methacryloxypropyltriethoxysilane, γ-aminopropyltrimethoxysilane, γ-aminopropyltriethoxysilane, 3-isocyanatopropyltriethoxysilane, or γ-acetoacetatetripropyltrimethoxysilane, which may be used alone or as mixtures.
The silane coupling agent may be present in an amount of 0.005 to 5 parts by weight based on 100 parts by weight of the acrylic resin. If the amount of the silane coupling agent is less than 0.005 parts by weight, the coupling agent does not effectively work. If the amount of the silane coupling agent is greater than 5 parts by weight, bubbles or peeling of the adhesive layer can occur due to coupling agent residues, thereby deteriorating durability.
The adhesive composition according to the present invention may further include a tackifier in order to adjust tack performance.
Examples of the tackifier may include, without being particularly limited to, for example, hydrocarbon resins or hydrogenated products thereof; rosins or hydrogenated products thereof; rosin esters or hydrogenated products thereof; terpene resins or hydrogenated products thereof; terpene phenolic resins or hydrogenated products thereof; and polymerized rosins or polymerized rosin esters, which may be used alone or as mixtures.
The tackifier may be present in an amount of 1 to 100 parts by weight based on 100 parts by weight of the acrylic resin. If the amount of the tackifier is less than 1 part by weight, the tackifier does not work properly. If the amount of the tackifier is greater than 100 parts by weight, improvement in compatibility or cohesion becomes insignificant, thus decreasing reliability of the adhesive layer or causing turbidity of the adhesive layer.
The adhesive composition according to the present invention may further include at least one additive selected from the group consisting of epoxy resins, UV stabilizers, antioxidants, toning agents, reinforcing agents, fillers, antifoaming agents, surfactants, and plasticizers so long as the additives do not affect aspects of the present invention.
There is no particular restriction as to a method of manufacturing the adhesive layers by curing the adhesive composition. In some embodiments, the adhesive composition or a coating solution prepared using the same is applied to a proper substrate using a typical instrument, e.g., a bar coater, and cured, thereby preparing an adhesive layer.
Curing may be carried out after volatile components or reaction residues are completely removed from the adhesive composition or the coating solution so as not to cause formation of bubbles. Accordingly, decrease in elastic modulus of the adhesive due to too low a crosslink density or molecular weight may be prevented. Further, it is possible to prevent formation of bubbles between adhesive layers, which can grow into scattering adherends.
There is no particular restriction as to a method of curing the adhesive composition or the coating solution. For example, curing may be carried out by properly heating the coating layer or aging the coating layer under predetermined conditions.
In the adhesive film, the sheet-form adhesive layer has a thickness of 15 to 100 μm, preferably 20 to 70 μm. Within this range, the adhesive film can not only be applied to a thin touch panel or touchscreen but have excellent heat resistance, optical characteristics, cuttability, workability, wettability, and durability.
The adhesive film of the present invention may further include a release film formed on one surface of the adhesive layer as necessary.
There is no particular restriction as to the kind of the release film to be used in the present invention, and any typical plastic films in the art may be used. Examples of the release film may include a PET film, a polytetrafluoroethylene film, a polyethylene film, a polypropylene film, a polybutene film, a polybutadiene film, a vinyl chloride copolymer film, a polyurethane film, an ethylene-vinyl acetate film, an ethylene-propylene copolymer film, an ethylene-ethyl acetate copolymer film, an ethylene-methyl acetate copolymer film, or a polyimide film. Further, one or both sides of the release film may be subjected to proper release treatment. Examples of a release agent used for release treatment may include alkyd, silicone, fluorine, unsaturated ester, polyolefin, or wax release agents. Among these, alkyd, silicone, and fluorine release agents may be used in terms of heat resistance, without being limited thereto.
The thickness of the release film is not particularly limited, but may be adjusted properly depending on purpose. For example, the release film has a thickness of 20 to 80 μm, preferably 30 to 70 μm.
The present invention also relates to a touch panel which includes a window film; the adhesive film according to the present invention attached to a lower surface of the window film; and a conductive laminate attached to a lower surface of the adhesive film.
A structure of the touch panel is not particularly limited so long as the adhesive film of the present invention is used to bond the window film and the conductive laminate.
Referring to
In the present invention, the conductive laminate may have a structure in which transparent plastic films 13a, 14a each having a conductive layer 13b, 14b formed on one surface thereof are disposed to be separated from each other, with the conductive layers 13b, 14b facing each other. In this case, opposite edges of conductive films 13 and 14 including the conductive layers 13b, 14b and the transparent plastic films 13a, 14a are bonded to each other via a double-sided adhesive tape (DAT) 15, with a space 16 defined therebetween.
In the present invention, there is no particular restriction as to the kind of each element constituting the touch panel 70, i.e., the window film, the conductive films, or the double-sided adhesive tape, and any element generally used in the art may be employed, without being particularly limited.
Further, the touch panel of the present invention may have a structure in which the conductive laminate is attached to a proper plastic substrate. In this case, the structure of the touch panel may be similar to that of the sample used for the writing test shown in
Hereinafter, the present invention will be explained in more detail with reference to examples according to the present invention and comparative examples. These examples are provided for illustrative purposes only and are not to be in any way construed as limiting the present invention.
65 parts by weight of ethylhexyl acrylate (EHA), 25 parts by weight of methyl acrylate (MA), and 10 parts by weight of acrylic acid (AA) were put into a 1L reactor equipped with a reflux condenser for supply of nitrogen gas and for easy temperature adjustment, and 100 parts by weight of ethyl acetate (EAc) as a solvent was added to the reactor. Then, after oxygen was purged from the reactor with nitrogen gas for 1 hour, the mixture was evenly stirred at 62° C., followed by addition of 0.03 parts by weight of azobisisobutyronitrile (AIBN) diluted with ethyl acetate to 50% as a reaction initiator. Subsequently, the mixture was reacted to prepare an acrylic resin (A) having a weight average molecular weight of 1,500,000.
An acrylic resin (B) having a weight average molecular weight of 2,000,000 was prepared in the same manner as in Preparative Example 1 except that reaction conditions including the content of the reaction initiator were properly adjusted.
An acrylic resin (C) having a weight average molecular weight of 800,000 was prepared in the same manner as in Preparative Example 1 except that reaction conditions including the content of the reaction initiator were properly adjusted.
A low molecular weight acrylic compound (E) having a weight average molecular weight of 5,000 was prepared using a monomer mixture including 90 parts by weight of a cyclohexyl methacrylate (CHMA) and 10 parts by weight of acrylic acid (AA) by properly adjusting preparation conditions in Preparative Example 1.
100 parts by weight of the acrylic resin (A) and 0.5 parts by weight of a bifunctional aziridine crosslinking agent as a polyfunctional crosslinking agent were mixed into an adhesive composition, which was then used to prepare a coating solution. The coating solution was applied to a release-treated surface of a release-treated PET film (thickness: 50 μm) to a thickness of about 50 μm after drying. The product was dried and aged under suitable conditions, thereby forming an adhesive layer having a thickness of 50 μm. Then, the adhesive layer was laminated to opposite sides of a PET film with a thickness of 12 μm, thereby producing a double-sided adhesive film.
100 parts by weight of the acrylic resin (B) and 0.5 parts by weight of a bifunctional aziridine crosslinking agent as a polyfunctional crosslinking agent were mixed into an adhesive composition, which was then used to prepare a coating solution. The coating solution was applied to a release-treated surface of a release-treated PET film (thickness: 50 μm) to a thickness of 50 μm after drying. The product was dried and aged under suitable conditions, thereby forming an adhesive layer having a thickness of 50 μm. Then, the adhesive layer was laminated to opposite sides of a PET film with a thickness of 12 μm, thereby producing a double-sided adhesive film.
100 parts by weight of the acrylic resin (C), 10 parts by weight of the low molecular weight acrylic compound (D) prepared in Preparative Example 4, and 0.5 parts by weight of a bifunctional aziridine crosslinking agent as a polyfunctional crosslinking agent were mixed into an adhesive composition, which was then used to prepare a coating solution. The coating solution was applied to a release-treated surface of a release-treated PET film (thickness: 50 μm) to a thickness of about 50 μm after drying. The product was dried and aged under suitable conditions, thereby forming an adhesive layer having a thickness of 50 μm. Then, the adhesive layer was laminated to opposite sides of a PET film with a thickness of 12 μm, thereby producing a double-sided adhesive film.
Physical properties of the adhesive films prepared in the examples and the comparative example were evaluated as follows.
1. Writing Test
A sample was prepared using each of the adhesive films prepared in the examples and the comparative example, as shown in
<Evaluation of Writing Test>
O: Passed the writing test 100,000 times or more.
X: Passed the writing test less than 100,000 times.
The results of the test are listed in Table 1.
As seen from Table 1, the adhesive films according to the inventive examples passed through the writing test 150,000 times or more, thereby exhibiting excellent surface press durability when actually applied to a touch panel.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2010-0031534 | Apr 2010 | KR | national |
This is a Continuation-In-Part of U.S. patent application Ser. No. 13/634,722 filed Sep. 13, 2012, which claims benefit to the national stage of PCT/KR2011/002359, filed Apr. 5, 2011, an application claiming the benefit to Korean Application No. 10-2010-0031534, filed on Apr. 6, 2010, the content of each of which is hereby incorporated by reference in its entirety.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 13634722 | Sep 2012 | US |
| Child | 14330503 | US |
