WO2010001492A1 - Anti-glare laminate - Google Patents
Anti-glare laminate Download PDFInfo
- Publication number
- WO2010001492A1 WO2010001492A1 PCT/JP2008/062365 JP2008062365W WO2010001492A1 WO 2010001492 A1 WO2010001492 A1 WO 2010001492A1 JP 2008062365 W JP2008062365 W JP 2008062365W WO 2010001492 A1 WO2010001492 A1 WO 2010001492A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- hard coat
- protrusion
- antiglare
- coat layer
- tends
- Prior art date
Links
Classifications
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/02—Diffusing elements; Afocal elements
- G02B5/0273—Diffusing elements; Afocal elements characterized by the use
- G02B5/0278—Diffusing elements; Afocal elements characterized by the use used in transmission
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/02—Diffusing elements; Afocal elements
- G02B5/0205—Diffusing elements; Afocal elements characterised by the diffusing properties
- G02B5/0236—Diffusing elements; Afocal elements characterised by the diffusing properties the diffusion taking place within the volume of the element
- G02B5/0242—Diffusing elements; Afocal elements characterised by the diffusing properties the diffusion taking place within the volume of the element by means of dispersed particles
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J2211/00—Plasma display panels with alternate current induction of the discharge, e.g. AC-PDPs
- H01J2211/20—Constructional details
- H01J2211/34—Vessels, containers or parts thereof, e.g. substrates
- H01J2211/44—Optical arrangements or shielding arrangements, e.g. filters or lenses
- H01J2211/442—Light reflecting means; Anti-reflection means
Definitions
- the present invention relates to a display C), a plasma display panel PDP), a brown (CR) display, and the like, and particularly to a high display.
- It is intended to provide excellent brightness, surface quality, transparency, gloss and prevention.
- it can be used for very high-definition C and PP like a high-definition spray full-split vision display in recent years, and is intended to provide a high-quality, black-colored image, excellent image quality, and low production.
- Et al. Conducted a study to satisfy all of these properties at the same time, and argued that it could not be achieved only by further adjusting the amount of particles or using particles having a diameter in combination. It came. In other words, in general, if the number of particles in the hard layer is increased or the size of the particles is increased in order to increase the level of the hard coat, the display becomes lower and the display becomes inferior. Become. In addition, it is inferior in blackness. Or reduce the amount of particles, If you do it, it will be inferior to, and it will impair your ability as a hadcot fill.
- the cloth width (W) plotting the degree of protrusion against the protrusion on the face of (B) is 500 m 50 below Is.
- the hardware (B) which will be described later, is laminated on at least one side, without A) which will be described later.
- the width of the cloth B) is lower than the value width W 50 50 of the cloth in which the degree of protrusion relative to the protrusion is plotted.
- the value width W of the protruding fabric and the fabric are the half value and the height of the surface profile obtained by the ZYGO product name V e 5022), plotting the projection), CO S) on the horizontal axis by so Po.
- the cloth When the gW of the cloth is in the above numerical range, the cloth is excellent in transparency, gloss, and prevention, and in the balance between these. In addition, can be reduced.
- the price range W is too small, the gloss tends to increase and tends to be inferior to. Also, tends to increase.
- the full width at half maximum W is more preferably below 5500 and particularly preferably below 700.00.
- the cloth value width W) plotting the degree of protrusion with respect to the protrusion degree and the cloth CS (s) satisfy the following () on the face (B).
- the fabric value width W and the fabric width are in the range satisfying the above (), can be further reduced.
- the fabric is preferably under 5000 Co s) Co S).
- the protrusion fabric is more preferably 8000 Co s) Co), particularly preferably 0000 Co) Co) on the side of the hardware B), which is the value width W of the protrusion fabric.
- the value range W of the protruding fabric and the particularly preferable method for ensuring that the fabric satisfies the above-mentioned conditions are the organic C) and content, inorganic () and content, inorganic) collections described below.
- the anti-hardware B) is suitable.
- the inorganic D) part is gathered in the protective B).
- the value width W of the protruding fabric tends to decrease, and at the same time, the protruding fabric tends to increase.
- Increasing the amount of C) tends to increase the protuberance.
- the amount of (D) is increased, the fabric width W tends to increase.
- it is effective to reduce the amount of organic C. For example, It is effective to reduce the amount to 3 ⁇ 5 or less.
- Such an embodiment having a surface waviness component in the face B) is preferable.
- the waviness component is different from the sharpness and indicates that it exists gently on the surface of the dot B.
- a surface undulation component is presumed to be formed by an assembly of an inorganic (non-inorganic), which will be described later.
- the size of such a surface undulation component is preferable. More preferably, 0 U 90, more preferably 20 U 85, particularly preferably 30 U, 50 m.
- the value width W of the protruding fabric may be further set to the above value.
- the surface roughness component can be easily formed by controlling the size of the inorganic material or the aggregate.
- the lower limit is more preferably 0 7 2 7, further preferably 0 ⁇ 9 upper ⁇ 9 lower, and particularly preferably • upper ⁇ 6 lower.
- this can be achieved by adjusting the amount of organic (C) and () described later, adjusting the ratio of organic (C), and adjusting the brightness of the organic (C).
- the degree in the dark side (B) is higher, more preferably 2.
- plastic fil- ter fills which have been conventionally used as optical hard coat fills.
- plastic films include polyethylene terephthalate, polyethylene terephthalate, polyester film made of polyethylene talate, etc., polyolefin film made of polyethylene, polypropylene, etc., cellophane, diacellulose film, triace cellulose film, ace cellulose.
- polyester fill is preferred, and polyester fill made of polyethylene terephthalate is particularly preferred because of its excellent mechanical properties, thermal properties, transparency, and processing. Also, biaxial fill is particularly preferred.
- the length of () is not particularly limited and depends on the situation, but it is usually below 2 5 000, preferably 50 is below 2 50. If the value is in the above range, the effect on transparency will increase. In addition, the properties are good and the handleability is excellent.
- A) in the description can be surface-treated for the purpose of improving the adhesion to B (such as improving adhesion with B.
- Such surface treatment includes sand blasting and surface treatment such as Surface treatment, corona treatment, lom treatment, flame treatment, hot air treatment, ozone / external irradiation, etc.
- ply treatment can be applied to the surface or both sides of).
- Hadkot (B) in Ming consists mainly of activated energy energy.
- Examples of the chemical engineering energy include external fats and electrons. From the viewpoint of ease of handling
- Such an outside line can be selected from conventional ones.
- This external line generally contains a photopolymerizable mono as a basic component, and further contains a polymerizable prepoly, a photopolymerization initiator and the like as desired.
- polymerizable monomers examples include: 4 butanediol metal methacrylate,, 6 hexanediol metal glycolate, neopentyl glycolide (metalylate, polyethylene glycol metalylrelate, neopentylglycol adipeptide is reretto, hydraline peptide N-glycol acrylate, penta acrylate, caprolaton terteni methacrylate, ethylene Oxidyl meta), allyl meta), isocyanurate di metal, trichloropropane tri metal, bentaerythritol trimethylate, propion pentaerythritol acrylate, pentaerythritol meta) And propioxide tritylpropylpropriate metal retlet, tris (ata isocyanurate, propion pentaerythritol pentarelet, pentaerythritol he
- the photopolymerizable prepoly may be, for example, a polyester arylate, an epoxy acetal, a urethane polymer, etc. DOO system, polio luer relay preparative system poly and the like.
- polyester A relay DOO system Purepori is obtained, for example, by the engagement of the polyhydric carboxylic polyhydric alcohols Le
- the acid group of the polyester oligo having a Z acid group can be obtained by esterifying with acrylic acid. Alternatively, it can be obtained by esterifying the acid group at the end of the oligo obtained by adding alkyloxy to polyvalent rubonic acid with metataric acid. For example, there is a relatively low sulfuroxy
- the urethane rellet-based prepoly can be obtained, for example, by esterifying a urethane oligo obtained by reacting with a polyesterpolyol polyesterpolyol isocyanate with methacrylic acid.
- the polyol acrylate prepolymer can be obtained by esterifying the acid group of the polyester polyol with oxalic acid.
- benzoin benzoin methyl ether
- benzoin ether benzoin ether
- benzoisopropyl ether benzoy
- Luether Benzyl ether, Acenone, Methylaminonone, 22 Toxyl-2 Ruatophenone, 2, 2 Toxinone, 2 Methyl lupropane on, Ton, Methyl 4IX Lucio ruphorino propane on, 4 2 Toxyl) 2 xy 2 pro J tonne, benzonone, 1 benzonone, 4, tilaminobenzonone / benzonone, 2 methylanthraquinone, 2 tilanthraquinone, 2 e tilanthraquinone, 2 aminoanthraquinone, 2 methylthioxanthone, 2 lutioxanthone 2 xanthone, 2, 4 methylthioxanthone, 2, 4
- Xanthone benzyl methyl ketal, acetophan dimethyl ketal, P methylamine benzoic acid steal, and the like. These may be used alone or in combination of two or more. Further, it is preferably 0 ⁇ 20 or less with respect to the polymerizable mono 00.
- 2 is up 0 down.
- the value By setting the value to the above value, the effect of improving the surface and can be enhanced. In addition, can be further reduced. If it is too sharp, the effect on surface quality tends to be low. Moreover, it is inferior to steel. Physically, when the thickness is less than 2, the pencil degree tends to be lower. On the other hand, if it is too thick, the surface tends to be high, but the added particles tend to be difficult to form protrusions.
- Hadkoto B is more preferably 3 m 8a or less, particularly preferably 4a 7 or less.
- the Hadkoto (B) has organic C) below 0 ⁇ 5 5 ⁇ 0 and inorganic below 30).
- An embodiment that contains 50 parts of the above and is gathered as part B) is particularly preferable. Furthermore, as will be described later, only the hardware (B) is used.
- the organic (C) is more preferably under 5 m 4 5a, more preferably under 2 4a, and particularly preferably under 2.5 m 3 5a.
- the amount of the organic (C) is preferably 0 ⁇ 55 5 or less based on the amount of the Hadkoto B).
- the amount of (C) is preferably 0 ⁇ 55 5 or less based on the amount of the Hadkoto B).
- the organic (C) in the photo includes polymethyl meta) relate, cross-linked polymer meta) relate, cross-linked methyl meta) releto styrene polymer polystyrene, cross-linked polystyrene, laminator, benzomine, polycarbonate, Polyvinyl children are preferred.
- a crosslinked (meta) reticule is preferable, and a polymer (reactive index) of 49 or more and 5 or less is more preferable.
- the folding ratio to the above value, the effect on transparency can be enhanced. This is particularly effective when a natural engineering energy having a refractive index of 49 to 5 is used.
- Such (C) preferably has a large diameter.
- those which do not form are preferable.
- the hardware B has an average of 5 above 60 below 0.
- inorganic is more preferably about 45 g, and particularly preferably 1 to 3 n.
- the inorganic content is below Rn, with the amount of hard coat (B) as the reference rt. )
- the amount of hard coat (B) as the reference rt.
- the above numerical value can increase the effect of transparency, gloss, and prevention, and can be excellent in the balance thereof. Moreover, can be further reduced.
- the content of inorganic (D) is preferably below 5 4, more preferably 38 44, particularly preferably 40 42 or less.
- the inorganic D) in the light is preferably a silica, a silica, an alumina, or a child.
- silica particles are preferable, and silica and primary particles are more preferable.
- an embodiment in which the inorganic part is gathered in the form of anti-protection B) is preferred.
- such an aspect is a particularly preferable means for setting the value width W of the protruding fabric on the surface of the hardware (B) to a value defined by Akira.
- this is a particularly preferable means for setting the value of the protrusion fabric to a value that is preferable for light.
- 50 or more, preferably 80 or more, are involved in the formation of secondary elements. Shows the case.
- the pre-collected inorganic material (which may be used or dispersed) is a process for preparing the formation of the Hadkoto B). At least one of the process, the process, the process of drying, and the process of drying may be formed.
- Dispersion (X) in which () is dispersed is about 2 in volume, preferably 3 in volume, and (Y) or Y) that is different from (X) is dispersed and inorganic) is dispersed in Y) Z addition
- inorganic materials For example, inorganic () When an average of 5-6 silica is used, inorganic () can be obtained by using toluene as X) and methyl as (Y). Thus, it is better to use X) as the comparative agent for inorganic) and (Y) as the comparative agent.
- the selection of can adjust the size of inorganic).
- the inorganic () 3 added after the dispersion corresponds to the inorganic () in the dispersion X) Z.
- the inorganic () bodies in Hadkot B preferably on 0 ⁇ 20, more preferably on 0 ⁇ 5 on 5, the inorganic () is more likely to form and the preferred surface condition in light Easy to form.
- the diameter of the inorganic material to be added later is preferably 5 to 60, more preferably g 45, and particularly preferably 5 to 30.
- an embodiment having a surface bending component in the aspect of the hardware is preferable.
- Such a surface bending component is presumed to be formed by the presence of an aggregate in which inorganic) or inorganic) is further aggregated in the hardware B.
- By setting the surface of the Hadkoto B) in such a manner it is formed smoothly in a portion where the organic C) is not present, and the gloss can be lowered and the brightness can be increased without deteriorating the transparency. Moreover, can be further reduced. If () is not collected, it will generally be sharply formed from inorganic () Z, and surface warping components Is not formed, and it becomes difficult to achieve excellent transparency, gloss, and prevention. Moreover, it becomes difficult to make these balances excellent.
- a reflection (E) made of a siloxane group, a hook or the like can be provided on the surface of the hardware B).
- the reflection (E) is preferably 0 ⁇ 0 upper and lower.
- a can be formed on the side of A) opposite to the hardware B).
- those which have been well used in conventional optical applications are preferable.
- talyl, uretan and silicon are preferred. Only this is usually 5 to 00, and preferably 10 to 50.
- a fill can be provided on this layer as needed.
- examples of such a film include those in which a silicone resin or the like is applied to a glassine, a koto, a minet, and a plastic film. The thickness of this film is not particularly limited, but is usually 0 to 1 0 0.
- It can be produced by preparing a material for forming a hard coat (B), forming the material on the substrate (), and then forming it by irradiation with an activated energy line.
- the conventional method should be used. You can. For example, bacot, knife, mouth, blade, die, and gravure can be used.
- 50 to 50 C is preferably between 0 and 50, 60 to 20 C is more preferably between 20 and 30, and 70 to 50.
- Examples of chemical engineering energy are outside lines and electrons.
- the external line is obtained with a high-pressure mercury lamp, a fusion lamp, a xenon lamp, etc., and the irradiation is usually 00 to 50 Jc. At this time, nitrogen purge is preferable. By padding, it is possible to prevent inhibition of oxidation due to oxygen damage on the surface of the hazard), and to increase the surface degree.
- the irradiation is usually 50 to 3 50 V.
- the outside line is particularly suitable from the viewpoint of handling. When electrons are used, they can be cured without adding polymerization initiation.
- Platinum is sputtered onto this surface to form platinum with a thickness of 200 to 30 A, and observed with a scanning microscope at ⁇ 3. Letta Co., Ltd., Zetta 500, asked for at least 00 children, and the average value of them was taken as the child's or).
- Aluminium is applied to the surface of the sample, and the surface is 20 using a mirror. 8
- the sample is fixed to a scanning microscope, and sputtering is performed on the sample surface using JE00 type ion sputtering (product name: JS00 type). Etching was performed for 5 hours. The platinum was sputtered at the same position, observed at ⁇ 5 using a scanning microscope, and judged by.
- the above work was carried out in terms of Hadokot B in.
- the particle size was determined from the particle size and based on the number of observed inorganic particles (), it was determined that agglomeration on the 50th was gathered.
- the surface was observed with an optical microscope and the thickness was measured. This was carried out at five arbitrary locations, and the average value was taken as the measured value.
- a 283 X2 area was scanned at a magnification of 25 times to obtain a surface profile. From the obtained surface profile, a cloth in which protrusions) and Co s) were plotted on the horizontal axis was obtained by SO a PO. From the resulting cloth, the kraft was defined as Co s of the protruding cloth. In addition, the width of the protruding fabric at the position of the pitch of the obtained fabric was defined as the half-value width W). The median value for the protrusions was calculated by the computer. In the aspect of B), the survey was conducted at five arbitrary locations, and the average value was taken as the measured value. 9
- Zumeta stock name 2000 was used and determined according to J674. We conducted the survey at five points in and, and set the average value of them as ().
- the 50-inch plasma display sold under the product name 5 PZ70) of the lower electrical appliance industry company was peeled off and attached with the adhesive obtained in the clear.
- the surface of the plus display was displayed in color, the number of was counted, and the following marks were used.
- Dispersion C Dispersed powder of cross-linked talyl particles having an average particle size of 3 m (manufactured by Soken Chemical Co., Ltd .: trade name MX300) in a methyl ethyl ketone solution, and a dispersion of organic particles (solid content concentration 0 mass / 0) Got.
- Dispersion solution C2 A powder of crosslinked ataryl particles having an average particle size of 4 was dispersed in a methyl ethyl ketone solution to obtain a dispersion solution C 2 of organic particles (solid content concentration 0 mass / 0).
- Dispersion solution C3 Powdered crosslinked talyl particles having an average particle diameter of 5 mm were dispersed in a methyl ethyl ketone solution to obtain a dispersion solution C 3 of organic particles (solid content concentration 0 mass / 0).
- Dispersion solution C4 A powder of crosslinked atalyl particles having an average particle diameter of 2 m was dispersed in a methyl ethyl ketone solution to obtain an organic particle dispersion solution C4 (solid content concentration 0 mass 0 / dispersion solution D: average particle diameter of 2On Dispersion solution D (solid content concentration 0 mass / 0) of inorganic particles was used as it was by using a dispersion solution (manufactured by C-I Kasei Co., Ltd .: trade name S IT 0WT%) in which silica particles were dispersed in toluene.
- a dispersion solution manufactured by C-I Kasei Co., Ltd .: trade name S IT 0WT% in which silica particles were dispersed in toluene.
- Dispersion solution D2 A dispersion solution in which silica particles having an average particle size of 40 n were dispersed in toluene was used as an inorganic particle dispersion solution D2 (solid content concentration: 0% by mass).
- Dispersion solution D3 A dispersion solution in which silica particles having an average particle diameter of 0 nm were dispersed in toluene was used as an inorganic particle dispersion solution D3 (solid content concentration: 0% by mass).
- Dispersion solution A dispersion solution in which silica particles having an average particle diameter of 50 nm were dispersed in toluene was used as an inorganic particle dispersion solution D4 (solid content concentration: 0 mass XO).
- Dispersion solution A dispersion solution in which silica particles having an average particle diameter of 70 nm were dispersed in toluene was used as an inorganic particle dispersion solution D5 (solid content concentration: 0 mass XO).
- D5 solid content concentration: 0 mass XO.
- Atallate ultraviolet ray JSR Co., Ltd., trade name LIGHT Z 750, solid 50, methyl ton, 20 having an average of 20 silica particles in solid 00) 00, methyl ton 0 were added. Thereto was added 5 C of dispersion C obtained above as organic C). The dispersion obtained above as inorganic () is 3.0
- Example 4 The result was obtained in the same manner as in Example 4 except that 0 o was used so that the dryness was 6/5.
- the table below shows the B and the sexes that were obtained. 6
- the dispersion C3 0 o obtained above is used as 5 ⁇ .
- the dispersion 3 obtained above (using 0 is used as The product was obtained in the same manner as in Example 1 except that it was used after standing at room temperature for 2 hours, and was processed so that the dryness was 4.0. Display 7
- Example 8 An antiglare laminate was obtained in the same manner as in Example 1 except that the amount was 33.0 parts by mass. Table 1 shows the constitution and properties of the obtained antiglare hard coat layer () and the antiglare laminate.
- dispersion solution C4 solid content concentration 0 mass X obtained above instead of dispersion solution C 1, the addition amount is 27 2 parts by mass, and addition amount of dispersion solution D is 6.3
- the coating thickness after drying and curing is 5 parts by weight.
- Example 1 An antiglare laminate was obtained in the same manner as in Example 1 except that the coating was applied to 0 m.
- Table 1 shows the constitution and characteristics of the obtained antiglare hard coat layer (B) and antiglare laminate. Comparative Example 1
- the antiglare laminate was prepared in the same manner as in Example 1 except that the amount of the dispersion solution (solid content concentration 0 mass / 0) was 5.1 parts by mass, and the inorganic particle dispersion solution was not added later. Obtained.
- the composition and properties of the obtained antiglare hard coat layer (B) and the antiglare laminate are shown in the table below. Comparative Example 2
- the added amount of the dispersion solution (solid content concentration 0 mass Xo) is 5.4 parts by mass, and instead of the dispersion solution D1, the dispersion solution D5 obtained above (solid content concentration 0 mass%) is used.
- An antiglare laminate was obtained in the same manner as in Example 1 except that the amount added was 38.0 parts by mass.
- Table 1 shows the constitution and characteristics of the antiglare hard coat layer (B) and the antiglare laminate in the obtained antiglare laminate.
- the value range of the protrusion fabric obtained in 8 to 8 was appropriate, and the transparency, gloss and prevention were excellent at the same time. In addition, there were few.
- the shape obtained in Examples 2 and 3 was particularly preferable, and was not observed.
- the value range of the protrusion fabric was inappropriate because the inorganic material (obtained in 2) was not collected. In other words, the shape was inappropriate. Therefore, although the transparency was high, the gloss was too high. In particular, a lot of brightness was measured.
- the value width of the protruding fabric obtained in 3 was too large. In other words, the shape was inappropriate. Therefore, although it was excellent in low gloss, it was inferior in transparency. 9
- Hexapropylene (P) n as the agent, Perfluoropropyl ether P 53 2 Ethyl ether VE 48/7 Hydro ether VE) 26 4, Lauroyl peroxide (PO
- Poly was taken out from the liquid using methanol, and ffuffed fat was obtained by vacuum.
- the reflection (E) Z is improved and the penetration of sunlight is reduced. Furthermore, because of improved light, improved.
- the image when attached to a commercially available pull-spetter high-definition plasma display through an appropriate optical lens obtained in the implementations 9 to 9, the image is excellent because of its blackness and sufficient gloss. It was excellent as a display, had a small amount, and was excellent as a display.
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- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Optical Elements Other Than Lenses (AREA)
- Laminated Bodies (AREA)
- Devices For Indicating Variable Information By Combining Individual Elements (AREA)
- Liquid Crystal (AREA)
Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/JP2008/062365 WO2010001492A1 (en) | 2008-07-02 | 2008-07-02 | Anti-glare laminate |
JP2010518872A JP5554707B2 (en) | 2008-07-02 | 2008-07-02 | Antiglare laminate |
KR1020107029008A KR20110052541A (en) | 2008-07-02 | 2008-07-02 | Anti-glare laminate |
CN2008801301827A CN102083617A (en) | 2008-07-02 | 2008-07-02 | Anti-glare laminate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/JP2008/062365 WO2010001492A1 (en) | 2008-07-02 | 2008-07-02 | Anti-glare laminate |
Publications (1)
Publication Number | Publication Date |
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WO2010001492A1 true WO2010001492A1 (en) | 2010-01-07 |
Family
ID=41465606
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2008/062365 WO2010001492A1 (en) | 2008-07-02 | 2008-07-02 | Anti-glare laminate |
Country Status (4)
Country | Link |
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JP (1) | JP5554707B2 (en) |
KR (1) | KR20110052541A (en) |
CN (1) | CN102083617A (en) |
WO (1) | WO2010001492A1 (en) |
Cited By (8)
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JP2010078886A (en) * | 2008-09-25 | 2010-04-08 | Fujifilm Corp | Anti-glare film, anti-reflection film, polarizing plate, and image display device |
JP2012218401A (en) * | 2011-04-13 | 2012-11-12 | Jsr Corp | Surface protective film |
JP2013025310A (en) * | 2011-07-18 | 2013-02-04 | Dongwoo Fine-Chem Co Ltd | Anti-glare hard coating film, polarizer having the same, and display device |
JPWO2011129378A1 (en) * | 2010-04-13 | 2013-07-18 | 旭化成イーマテリアルズ株式会社 | Self-supporting film, self-supporting structure, manufacturing method of self-supporting film, and pellicle |
JP2015044302A (en) * | 2013-08-27 | 2015-03-12 | 三菱樹脂株式会社 | Transparent laminated film and transparent substrate |
WO2015163328A1 (en) * | 2014-04-23 | 2015-10-29 | 大日本印刷株式会社 | Method for producing laminate, laminate, polarizing plate, image display device, and method for improving readability of image display device |
JP2016103018A (en) * | 2011-12-26 | 2016-06-02 | 大日本印刷株式会社 | Antiglare film, polarizing plate and image display device |
JP2018176536A (en) * | 2017-04-12 | 2018-11-15 | 日油株式会社 | Antiglare antireflective film for insert molding and application of the same |
Families Citing this family (1)
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TWI719851B (en) * | 2014-07-18 | 2021-02-21 | 日商大日本印刷股份有限公司 | Optical film and display device with touch panel |
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- 2008-07-02 KR KR1020107029008A patent/KR20110052541A/en not_active Application Discontinuation
- 2008-07-02 CN CN2008801301827A patent/CN102083617A/en active Pending
- 2008-07-02 JP JP2010518872A patent/JP5554707B2/en active Active
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Also Published As
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CN102083617A (en) | 2011-06-01 |
JP5554707B2 (en) | 2014-07-23 |
KR20110052541A (en) | 2011-05-18 |
JPWO2010001492A1 (en) | 2011-12-15 |
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