CN101226254A - Ultra-low slow-moving optical film and polarization board containing said optical film - Google Patents

Ultra-low slow-moving optical film and polarization board containing said optical film Download PDF

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Publication number
CN101226254A
CN101226254A CNA2007100039270A CN200710003927A CN101226254A CN 101226254 A CN101226254 A CN 101226254A CN A2007100039270 A CNA2007100039270 A CN A2007100039270A CN 200710003927 A CN200710003927 A CN 200710003927A CN 101226254 A CN101226254 A CN 101226254A
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Prior art keywords
blooming
light
sluggish
ultralow
epoxy resin
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CNA2007100039270A
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Chinese (zh)
Inventor
陈世明
李永仁
李宗铭
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Industrial Technology Research Institute ITRI
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Industrial Technology Research Institute ITRI
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Priority to CNA2007100039270A priority Critical patent/CN101226254A/en
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Abstract

The invention discloses a ultra low retardation optical film, which mainly comprises nanometer metal oxides dispersed in transparent resin with three-dimension crosslink structure. The Ro in-plane retardation of the optical film is 0-2nm, the Rth out-of-plane retardation approaches 0nm, therefore, the invention can be used to replace traditional cellulose triacetate cta protective film of polarization plate, to resolve the problems of liquid crystal display under large angle as reduced black-white contrast and color change.

Description

Ultra-low slow-moving blooming and the Polarizer that contains this blooming
Technical field
The present invention relates to ultra-low slow-moving blooming and the application of this blooming in polarizing plate protective film.
Background technology
LCD (LCDs) has been widely used on individual computer monitor, digital camera and mobile phone and the large-sized TV.In the LCD panel, Polarizer (Polarizer) is one of fundamental parts of LCD.Polarizer is the tabula rasa that the light of a kind of a certain direction of permission sees through, in the process of making liquid crystal board, must each use a slice up and down, and become alternate directions to insert, main application produces the state that phasic difference presents light and shade for make light source when electric field is arranged with no electric field, to show captions or pattern.Along with the increase of LCD consumption, the Polarizer demand grows with each passing day.The polarization system of light polarizing film is by due to each anisotropy absorber of the light that directive property is arranged in the transparent polymer film, for example the polaroid of polyvinyl alcohol (PVA) (PVA) is after being adsorbed on iodine or a kind of two look dyestuffs in the polyvinyl alcohol film, makes the directive property of its tool single shaft by extension.Expansion along with LCD product usable range; requirement to the damp and hot condition of work of polarisation product is more and more harsher; the polaroid of doing with these materials runs into the problem of dimensional contraction easily in damp and hot reliability testing; the reason of optical characteristics deterioration is because the molecular structure of iodine is easy to destroyed event under hot and humid condition; so light polarizing film needs two surface protective films as supporting and protection; with permanance and the physical strength that keeps it, normally used diaphragm is Triafol T (TAC).These diaphragms need high transmittance, low-birefringence, outstanding heat, cold, light, moisture resistibility and optic homogeneity, that is to say, must no foreign object or the flaw of visual speckle.And with the Triafol T diaphragm of solvent method coating because of its penetrability, outward appearance is good and easy and light polarizing film is pasted so use so far.
Because the TV of large-scale LCD is popularized gradually, has required the TAC diaphragm to have lower birefringence.The Ro value (light hysteresis (in-plane-retardation) in the plane) of TAC is little at present, but Rth value (light hysteresis outside the plane (out-of-plane retardation)) is still big.This Rth value will cause that faulty optical compensation effect is arranged on the LCDs (for example has the contrast decline of black and white and color change (color shift) problem to take place under the wide-angle.Therefore the Rth value need heal better little, particularly on the LCD of IPS (plane internal conversion (in-plane switching)) pattern.Usually, polymkeric substance has its birefringence, and its value raises along with the strand directionality in the polymkeric substance and increases, and Rth value is to be difficult to reduce, and (in-plane) arranges event on the isoplanar because of the strand of polymkeric substance easily tends to.Therefore, in order to reduce birefringence, the method for general using compensation, for example Japan has researched and developed the polymkeric substance (WO2006098517 of zero birefraction (zero-birefringence) recently; JP2006096793), it compensates the positive birefringence of polymkeric substance by using negative birefringence inorganics crystal or adjuvant, to modulate the polymeric blends of zero birefraction.Cyclic olefin polymer (Cyclo the OlefinPolymer) (JP2006124628 that the performance low-birefringence is also arranged; US2004099973; JP2004168063), but its chemical framework is hydrophobic backbone and side chain, if be used for the PVA polarizing plate protective film, they almost are difficult to attached on the hydrophilic PVA.
Summary of the invention
Fundamental purpose of the present invention just provides a kind of ultra-low slow-moving blooming, to improve the optical compensation effect of LCD under wide-angle.
In order to reach above-mentioned and other purpose, ultra-low slow-moving blooming of the present invention mainly comprises: light-transmissive resin, and it has three-dimensional cross-linked structure; And, be scattered in the nanosize metal oxide particle in this light-transmissive resin; Wherein, light hysteresis (Ro in the plane of this blooming; In-plane retardation) between 0~2nm, light sluggishness (Rth outside the plane; Out-of-plane retardation) value is near 0nm.
The present invention also provides Polarizer, mainly comprises polaroid and above-mentioned ultra-low slow-moving blooming, and this blooming is arranged at least one surface of polaroid, with as polarizing plate protective film.
Description of drawings
Fig. 1 is the structural representation of the sluggish blooming of the ultralow light of the present invention.
Fig. 2 is a kind of device that can be used to make above-mentioned blooming.
Fig. 3 is a kind of Polarizer of using above-mentioned blooming.
Fig. 4 is a kind of display of using above-mentioned Polarizer.
Fig. 5 is the measurement result of the birefringence of the blooming of embodiment and TAC commodity.
Reference numeral
The sluggish blooming 16~curing system of 10~ultralow light
10a~light-transmissive resin 17~take-up roller
10b~nanometer particle 5~polaroid
12~groove 11~anti-dazzle film or anti-reflective film mix
13~apparatus for coating, 20~diaphragm
14~release film, 30~Polarizer
15~driving rolls, 40~liquid crystal panel
50~LCD
Embodiment
The Main Ingredients and Appearance of ultra-low slow-moving blooming of the present invention is the material that blendes together of high light-transmissive resin and the surperficial and inner nanosize metal oxide particle that is dispersed in this light-transmissive resin layer, can be referred to as nano composite material again.
As shown in Figure 1, ultra-low slow-moving blooming 10 of the present invention is a compound substance, and its composition comprises light-transmissive resin 10a and the nanosize metal oxide particle 10b that is dispersed in the resin.Light-transmissive resin 10a used in the present invention is to be the three dimensions cross-linked structure after reaction is solidified, so strand non-directive almost completely, is the isotropy that possesses optics, and institute thinks the zero birefraction transparent material of excellence.In addition, nanometer particle 10b is evenly distributed among the light-transmissive resin 10a, except itself having optic isotropy, also can upset the directive property of strand, thereby increases optic isotropy.On the other hand, mixing of nanometer particle 10b also can be improved hardness, thermal dimensional stability, water wettability and be reduced moisture vapor transmission rate.
The used light-transmissive resin of the present invention has the transmittance more than 90%, is mainly epoxy resin or acrylate resin, and suitable epoxy resin comprises have oxirane ring monomer, oligomer or the polymkeric substance of (oxirane ring).Preferred concrete example comprises: bisphenol A type epoxy resin (bisphenol A epoxyresin), bisphenol F epoxy resin (bisphenol F epoxy resin), bisphenol-s epoxy resin (bisphenolS epoxy resin), phenolic aldehyde Novolak epoxy resin, cresols Novolak epoxy resin, alicyclic epoxy resin or the naphthalene type epoxy resin of nitrogenous or hydrogenation and biphenyl type epoxy resin or the like.These epoxy resin can be separately or mixed the use, should look required processing transitivity and suitably select and allocate.Used acrylate resin comprises monomer whose, oligomer or polymkeric substance, preferred concrete example comprises: epoxy acrylate, polycarbamate acrylate, polyester acrylate, 1,6 hexanediol diacrylate (HDDA), hydroxyethyl meth acrylate (HEMA) or the like.Equally, these acrylate resins can use either alone or in combination, even use with the collocation of above-mentioned epoxy resin, should look required processing transitivity and suitably select and allocate.
Light-transmissive resin of the present invention also comprises rigidizer, and this rigidizer can be divided into thermal initiator and ultraviolet initiator two big classes, all availablely is used for the present invention separately or with hybrid mode.For epoxy resin system, thermal initiator can be selected acid anhydrides and the esterified anhydride rigidizer of part, as hexahydrophthalic anhydride (hexahydrophthalic anhydride; HHPA), tetrabydrophthalic anhydride (tetrahydrophthalic anhydride; THPA), methyl tetrahydrophthalic anhydride (methyltetrahydrophthalic anhydride; MTHPA), methylhexahydrophthalic anhydride (methylhexahydrophthalic anhydride; MHHPA); Triethylene diamine; Imidazolium compounds is as 2-ethyl-4-methylimidazole, glyoxal ethyline; Phosphorus compound is as triphenyl phosphorus (triphenylphosphine), tetraphenyl boric acid tetraphenyl phosphine (tetraphenylphosphonium tetraphenylborate), o-diethyl phosphorothioate (o-diethylphosphorodithioate); Quaternary ammonium salt etc.And uv initiator can be selected cationic metallic compound, as triaryl sulphur hexafluoro antimonate (triarylsulphoniumhexafluoroantimonite), triaryl sulphur hexafluorophosphate (triarylsulphoniumhexafluorophosphate), diaryl group iodized salt etc.For the acrylate resin system, uv initiator can be selected the light trigger of free radical type, as ketone (ketone) series, phosphine (phosphine) series etc.UV cured dose: the weight ratio of epoxy resin/acrylate resin is preferably between 0.03: 0.15, more preferably between 0.05: 0.1.Thermoinitiators: the weight ratio of epoxy resin/acrylate resin is preferably between 0.6: 1.3, more preferably between 0.9: 1.1.
Transparent resin of the present invention can optionally add other tradition adjuvant commonly used, for example can add plasticiser, to increase processability, ductility and the availability of transparent resin, its addition is generally between 10~50phr ((per 100 parts of resins) per hundred resin).
Than the linear molecular chain structure of traditional Triafol T (TAC), the molecule of resin system of the present invention is to be the three dimensions cross-linked structure after reaction, therefore strand non-directive almost completely, thereby possess the isotropy of optics, institute thinks the transparent material of the zero birefraction of excellence.Moreover the thermal dimensional stability of cross-linked structure is preferable, and the glass transition temperature that modulation can obtain hardening thing according to different prescription so can obtain the good transparent optical membrane material of thermal dimensional stability between 80~190 ℃.
The mean grain size of nano-metal-oxide particle of the present invention more preferably can be between 5~20 nanometers between 1~50 nanometer.Because nano particle diameter is less than 50 nanometers and be dispersed in the light-transmissive resin layer, so light can not be scattered and reflect when passing through nano composite material, can reach the transmittance (transmittance entirely) 90% or more.Suitable nano-metal-oxide particle includes but not limited to: silicon dioxide (SiO 2), titania (TiO 2), zirconium dioxide (ZrO 2), aluminium oxide (Al 2O 3), zinc paste (ZnO) magnesium oxide (MgO) etc.Above-mentioned nano particle can also use except can using separately in two or more mixing.
Because the thermal expansivity of nano-metal-oxide particle is lower,, so can obtain the good transparent optical film of flatness and thermal dimensional stability so the thermal expansivity of nano composite material of the present invention is lower than general known thermoplasticity blooming.In addition, traditionally in order to protect the surface of Polarizer, generally all can be coated with the hard layer (hard coat layer) of thick approximately 5~10 μ m of one deck on Polarizer, material is generally epoxy resin or acrylate resin.And the nano-metal-oxide particle that the present invention adds just has the very high characteristic of hardness in essence, can compensate the weakness of resin soft, so the hardness of nano composite material of the present invention is more than general known thermoplasticity blooming height, the high rigidity (pencil hardness is greater than 3H) of homogeneous and the transparent optical film of abrasion performance in so can obtaining to show, and do not need extra hard layer.In addition, the nano-metal-oxide particle can increase the water wettability of material, with the applying adhesive strength between increase and the polaroid.
The content of nano particle preferably between 5~50 weight %, more preferably between 10~30 weight % (gross weight with blooming is a benchmark).According to studies show that of the inventor, as long as the size of nano particle is enough little, its content number can't badly influence transmittance, though therefore generally do not need, the content of nano particle also might surpass 50 weight %.In addition, solid powder or the solution state product in the commercialization can be selected in the source of nano particle.
Except mentioned component, blooming of the present invention also can add conventional antioxidant or UV absorbers, and is rotten and guarantee the fiduciary level of Polarizer to avoid diaphragm.For example, but add the following ultraviolet light of absorbing wavelength 380nm after the UV absorbers.Antioxidant and UV absorbers can be added individually or simultaneously, and general addition is about 0.1-3 weight % (gross weight with blooming is a benchmark).
Fig. 2 is a kind of device that can be used to make above-mentioned blooming.It should be noted that the device of this figure only is used for illustrating, blooming of the present invention is not limited to install formed blooming by this.At first, all raw materials are weighed up according to formula rate insert in the groove 12 that mixes, be uniformly mixed to form slurry.According to the present invention, this slurry can be solvent-free (solid content 100%) or solvent-laden system (more than the solid content 40 weight %); The viscosity of preferred slurry is between 200~6000cp, so that follow-up coating operation.Injection apparatus for coating 13 (roller or die head) accurately was coated with on release carrier film 14 with the thickness of setting after slurry mixed, release carrier film 14 after the coating via the drive of driving rolls 15 with constant speed, promptly about 0.5 to 10m/min speed is by curing system 16, as oven heat or ultraviolet irradiation zone, the coating sclerosis is shaped after take-up roller 17 is batched.Formed transparent optical diaphragm is shown in 18, and under rerum natura and the dual consideration of cost, its suitable thickness is between 10~100 μ m, preferably between 20~80 μ m.
Release carrier film 14 can be mirror face stainless steel band or thermoplasticity glued membrane, as carbamate resins, acrylate resin, vibrin, polyvinyl alcohol (PVA), vinyl-vinyl alcohol copolymer (ethylene-vinylalcohol copolymer), vestolit, vinylidene chloride (vinylidenechloride) resin, cyclic olefine copolymer (MCOC) resin, polycarbonate resin, polyarylate (polyarylate) resin etc.
Fig. 3 is the application of the sluggish blooming of ultralow light of the present invention as polarizing plate protective film.As shown in Figure 3, Polarizer 30 comprises polaroid 5, is clipped between first diaphragm 10 (the sluggish blooming of ultralow light) and second diaphragm 20.Transparent optical diaphragm of the present invention can be arranged on the single face or the upper and lower surface of polaroid.Therefore, the material of second diaphragm 20 among Fig. 3 can be the sluggish blooming of ultralow light of the present invention, but also can be traditional diaphragm, for example cellulose ester, polycarbonate, acryl, polyester, polyolefin, norborene etc.Polaroid 5 used herein there is no specific restriction, as long as it has the characteristic of polarisation, for example is polyvinyl alcohol (PVA) (PVA) or polyenoid (polyene) polaroid.Transparent optical diaphragm 10 of the present invention, under rerum natura and the dual consideration of cost, its suitable thickness is between 10~100 μ m, preferably between 20~80 μ m.In addition, on diaphragm 10, also can form anti-dazzle film (AG) 11, between preferably about 2~10 μ m of thickness, or anti-reflective film (AR) 11, between preferably about 0.1~0.2 μ m of thickness.
Traditional Polarizer causes polarisation ability deterioration owing to the moisture resistibility of diaphragm is not enough, and can improve the optics fiduciary level of Polarizer by transparent optical film of the present invention, particularly under the environment of high humility.In a preferred embodiment, diaphragm of the present invention can reach 60~70g/m 2The moisture vapor transmission rate that/24hr is following is about about 1/6 of Triafol T diaphragm commonly used.
Diaphragm 10,20 can utilize clear binder or pressure-sensitive bonding agent and polaroid 5 to fit and form.In addition, in order to strengthen follow-up and polaroid applying adhesive strength, can do pre-surface handles, as plasma, corona, primary coat (as the PU primary coat) etc., because the structure and the composition of this compound substance, afterwards have good water wettability in its surface through processing such as plasmas, corona, its water contact angle can be less than 15 °, so can strengthen and essence is applying adhesive strength between the hydrophilic polaroid.
Polarizer of the present invention can use with other blooming collocation when practical application, for example reflectance coating, half-transparent half-reflection film, phase shift films (1/2 wavelength and 1/4 wavelength), compensation film for angular field of view etc.For example, Polarizer of the present invention can be fitted with reflectance coating or half-transparent half-reflection film and be formed reflection-type Polarizer or half-transparent half-reflection type Polarizer; Or fit to form ellipse or circularly polarizing plate with phase shift films; Or fit with compensation film for angular field of view and form the wide-angle Polarizer; Perhaps, fit with brightness enhancement film.
Polarizer of the present invention can be applied in various displays, includes but not limited to: LCD, display of organic electroluminescence, plasma display etc.For example, shown in the LCD 50 of Fig. 4, Polarizer 30 of the present invention can be arranged on the arbitrary surface or the opposite sides of liquid crystal panel 40.The kenel of liquid crystal and type of drive also do not have special restriction, can be TN (twisted-nematic) type liquid crystal, vertical orientation type liquid crystal, IPS (transverse electric field switching) liquid crystal etc.In addition, the formation of liquid crystal panel also comprises diffuser plate, prism array, backlight assembly etc. usually, does not repeat them here.
After tested; the Ro light hysteresis of ultra-low slow-moving blooming of the present invention can be between 0~2nm (incident angle is-40 °~40 °); Rth light hysteresis then is bordering on 0nm; and transmittance is not less than 90% (full transmittance); therefore can be used to replace the Triafol T diaphragm of traditional light polarizing film, improving LCD has the contrast decline of black and white and the problem of color change (color shift) under wide-angle.
By above explanation as can be known, the material that blendes together of the present invention possesses outside the optical characteristics of zero birefraction and high transmission rate, also possess the resistibility of outstanding hot and cold, moisture simultaneously, available non-solvent method is coated with and makes film on processing procedure, has advantages such as optic homogeneity, environmental protection and cost economy.
For above and other objects of the present invention, feature and advantage can be become apparent, hereinafter the spy enumerates preferred embodiment, is described in detail below.Employed nano particle is that NissanChemical company is produced among the embodiment " MEK-ST ", be a kind of methyl ethyl ketone (MEK) silicon dioxide gel (silica sol), and the dioxide-containing silica in the integral material prescription is controlled at 15 weight %.
[embodiment]
Thermal initiator methylhexahydrophthalic anhydride (MHHPA) is dissolved in the MEK silicon dioxide gel, adds epoxy resin EL-4221 (Union Carbide) and plasticiser Triol (Union Carbide) again and form slurry.Thermal initiator: epoxy resin: the weight ratio of plasticiser is 1: 1: 0.1.Slurry is placed in the vacuum drying oven deaeration and removed the MEK solvent to suitable solid content and viscosity, then coating is applied on the Arton substrate by the continuous coating machine of precision, after the baking oven sclerosis, can get the product of rolling.
Formed blooming of embodiment and commodity TAC film are measured through KOBRA-21ADH birefringence analyser (Optical birefringence Analyzer made by Oji Scientific Instruments), and the result is (phasic difference is to incident angle) as shown in Figure 5.As calculated, the average Rth value of commodity TAC film is up to 46nm, and the Rth value of the sluggish blooming of ultralow light of the present invention is then near 0nm.
Through measuring other character of embodiment blooming, comprise moisture vapor transmission rate, transmittance, hardness, surfaceness, water contact angle etc., every data of gained and traditional TAC film compare side by side, and be as shown in the table.
Figure A20071000392700111
The data presentation of last table, composite wood blooming of the present invention has preferable moisture opposing rate, hardness and surface contact angle than known TAC diaphragm; And the needed characteristic of other polarizing plate protective film, for example penetration, light retardation, surfaceness etc. are also poor unlike TAC.
Though the present invention discloses as above with several preferred embodiments, so it is not in order to limit the present invention.Any the technical staff in the technical field of the invention, without departing from the spirit and scope of the present invention, Ying Kezuo changes arbitrarily and retouching.Therefore, protection scope of the present invention should be as the criterion with appended claims institute restricted portion.

Claims (26)

1. sluggish blooming of ultralow light comprises:
Light-transmissive resin, it has three-dimensional cross-linked structure; And
Be scattered in the nanosize metal oxide particle in this light-transmissive resin;
Wherein, light hysteresis (Ro) is between 0~2nm in the plane of this blooming, and light hysteresis (Rth) is near 0nm outside the plane.
2. the sluggish blooming of ultralow light as claimed in claim 1, wherein this light-transmissive resin is epoxy resin or acrylate resin or aforesaid combination.
3. the sluggish blooming of ultralow light as claimed in claim 2, wherein this epoxy resin is selected from bisphenol A type epoxy resin, bisphenol F epoxy resin, bisphenol-s epoxy resin, phenolic aldehyde Novolak epoxy resin, cresols Novolak epoxy resin, alicyclic epoxy resin or the naphthalene type epoxy resin and the biphenyl type epoxy resin of nitrogenous or hydrogenation.
4. the sluggish blooming of ultralow light as claimed in claim 2, wherein this acrylate resin is selected from epoxy acrylate, polycarbamate acrylate, polyester acrylate, 1,6 hexanediol diacrylate (HDDA), hydroxyethyl meth acrylate (HEMA).
5. the sluggish blooming of ultralow light as claimed in claim 1, wherein this light-transmissive resin comprises: thermosetting macromolecule, ultraviolet curing type macromolecule or aforesaid combination.
6. the sluggish blooming of ultralow light as claimed in claim 1, wherein the glass transition temperature of this light-transmissive resin is between 80-190 ℃.
7. the sluggish blooming of ultralow light as claimed in claim 2, wherein this light-transmissive resin also comprises rigidizer.
8. the sluggish blooming of ultralow light as claimed in claim 7, wherein this rigidizer is thermal initiator or ultraviolet initiator rigidizer.
9. the sluggish blooming of ultralow light as claimed in claim 1, its transmittance is more than 90%.
10. the sluggish blooming of ultralow light as claimed in claim 1, wherein the particle diameter of this nanosize metal oxide particle is between 1~50nm.
11. the sluggish blooming of ultralow light as claimed in claim 1, wherein the particle diameter of this nanosize metal oxide particle is between 5~20nm.
12. the sluggish blooming of ultralow light as claimed in claim 1, wherein this nanosize metal oxide particle comprises: silicon dioxide (SiO 2), titania (TiO 2), zirconium dioxide (ZrO 2), aluminium oxide (Al 2O 3), zinc paste (ZnO), magnesium oxide (MgO) or aforesaid combination.
13. the sluggish blooming of ultralow light as claimed in claim 1, wherein this nanosize metal oxide particle accounts for 5~50 weight % of this blooming.
14. the sluggish blooming of ultralow light as claimed in claim 1, its pencil hardness is not less than 3H.
15. the sluggish blooming of ultralow light as claimed in claim 1, its aqueous vapor permeability is less than 80g/m 2/ day.
16. the sluggish blooming of ultralow light as claimed in claim 1, its surface water contact angle after treatment is less than 15 °.
17. the sluggish blooming of ultralow light as claimed in claim 1 also comprises: UV absorbers, antioxidant or aforesaid combination.
18. the sluggish blooming of ultralow light as claimed in claim 1, its thickness is between 10~100 μ m.
19. a Polarizer comprises polaroid, and the sluggish blooming of ultralow light as claimed in claim 1, this blooming is arranged on the surface of this polaroid, with as polarizing plate protective film.
20. Polarizer as claimed in claim 19, wherein another surface of this polaroid is provided with Triafol T as polarizing plate protective film.
21. Polarizer as claimed in claim 19, wherein the sluggish blooming of this ultralow light is arranged at the upper and lower surface of this polaroid.
22. Polarizer as claimed in claim 19, wherein no extra hard layer on the sluggish blooming of this ultralow light.
23. Polarizer as claimed in claim 19, wherein the sluggish blooming of this ultralow light combines with this polaroid with clear binder or pressure-sensitive bonding agent.
24. Polarizer as claimed in claim 19, wherein the thickness of the sluggish blooming of this ultralow light is between 10~100 μ m.
25. Polarizer as claimed in claim 19 wherein also comprises anti-dazzle film or anti-reflective film on the sluggish blooming of this ultralow light.
26. Polarizer as claimed in claim 19, wherein this polaroid is polyvinyl alcohol (PVA) (PVA) polaroid.
CNA2007100039270A 2007-01-18 2007-01-18 Ultra-low slow-moving optical film and polarization board containing said optical film Pending CN101226254A (en)

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102460282A (en) * 2009-04-24 2012-05-16 富士胶片株式会社 Liquid crystal display apparatus and liquid crystal cell
CN101586031B (en) * 2009-04-09 2013-07-03 深圳华映显示科技有限公司 Liquid crystal complex and preparation method thereof
CN103257388A (en) * 2012-02-21 2013-08-21 江苏华天通纳米科技有限公司 Nano-composite polarized lens
CN107109101A (en) * 2014-10-16 2017-08-29 株式会社Lg化学 Optical film application composition and the optical film comprising it
CN111051356A (en) * 2017-09-01 2020-04-21 三键有限公司 Photocurable composition

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101586031B (en) * 2009-04-09 2013-07-03 深圳华映显示科技有限公司 Liquid crystal complex and preparation method thereof
CN102460282A (en) * 2009-04-24 2012-05-16 富士胶片株式会社 Liquid crystal display apparatus and liquid crystal cell
US8715792B2 (en) 2009-04-24 2014-05-06 Fujifilm Corporation Liquid-crystal display device and liquid-crystal cell
CN102460282B (en) * 2009-04-24 2015-01-21 富士胶片株式会社 Liquid crystal display apparatus and liquid crystal cell
CN103257388A (en) * 2012-02-21 2013-08-21 江苏华天通纳米科技有限公司 Nano-composite polarized lens
CN103257388B (en) * 2012-02-21 2015-05-13 江苏华天通纳米科技有限公司 Nano-composite polarized lens
CN107109101A (en) * 2014-10-16 2017-08-29 株式会社Lg化学 Optical film application composition and the optical film comprising it
CN107109101B (en) * 2014-10-16 2019-07-23 株式会社Lg化学 Optical film application composition and optical film comprising it
CN111051356A (en) * 2017-09-01 2020-04-21 三键有限公司 Photocurable composition
US11739168B2 (en) 2017-09-01 2023-08-29 Threebond Co., Ltd. Photocurable composition

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