CN101792500A - Polymerizable composition and optical film comprising same - Google Patents

Polymerizable composition and optical film comprising same Download PDF

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CN101792500A
CN101792500A CN200910178872A CN200910178872A CN101792500A CN 101792500 A CN101792500 A CN 101792500A CN 200910178872 A CN200910178872 A CN 200910178872A CN 200910178872 A CN200910178872 A CN 200910178872A CN 101792500 A CN101792500 A CN 101792500A
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polymerisable compound
weight
monomer
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叶昆明
石一中
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Eternal Materials Co Ltd
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Eternal Chemical Co Ltd
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Abstract

The invention relates to a polymerizable composition and an optical film comprising the polymerizable composition. The polymerizable composition comprises (a) 1 to 90 weight percent of a monomer of a formula (I) and (b) 0.1 to 10 weight percent of a photo-initiator based on the total weight of the polymerizable composition, wherein X1, X2, X, R1, d and n are as defined in a specification. The invention also relates to another type of coating comprising the optical film formed by the polymerizable composition, and the optical film can be used in a backlight module of a display to serve as a brightening film.

Description

Polymerisable compound and comprise the blooming of this polymerisable compound
Technical field
The present invention relates to a kind of polymerisable compound and a kind of blooming that comprises by the formed coating of described polymerisable compound, this blooming can be used in the backlight module (BLU) of indicating meter as brightness enhancement film.
Background technology
Liquid-crystal display (Liquid Crystal Display, LCD), have light, thin, short, little, low thermal losses, low power consumption and advantage such as radiationless injury almost, replaced conventional cathode ray tube (Cathode Ray Tube at present, CRT) indicating meter becomes the market mainstream.
In backlight module, utilize blooming miscellaneous to improve panel briliancy (luminance), become most economical and easy product development scheme, mode not only must not changed any component design according to this, must not consume additional energy source yet, and can improve LCD panel briliancy and make light source do the performance of full blast.
Brightness enhancement film is called for short BEF (Brightness Enhancement Film) usually or claims condensing film, and it can be coated with special acryl resin coating by on polyester substrate, utilizes high-energy ultraviolet ray (UV) that it is hardened into prism microstructure and makes.The major function of brightness enhancement film is by the effect of refraction with inner full-reflection, will collect and be concentrated to positive visual angle (On-Axis) direction of degree approximately ± 35 by the ghost line that light guiding plate (Light Guide) is issued to from all directions, to improve the briliancy of LCD.
General brightness enhancement film commonly used is to utilize the ultraviolet curing polymeric composition, generally speaking selects the polymeric composition coating of high index for use, and the brightening effect of brightness enhancement film is good more.
At present known to adding halogen-containing monomer or oligopolymer in polymerisable compound, obtaining to have the polymeric composition coating of high index, yet the existence of halogen can cause environmental pollution.
In addition, can utilize 4,4 '-two (methacrylic vinegar sulfenyl) diphenyl sulfide (4,4 '-bis (methacroylthio) diphenyl sulfide, MPSMA) monomer, structural formula is as follows:
For example United States Patent (USP) discloses this monomer synthetic method for No. 5183917 and contains its composition, and the MPSMA monomer is a crystalline solid, has high refractive index, but shortcoming is to be insoluble in other monomer, is unfavorable for coating; No. 5969867 announcement of United States Patent (USP) utilizes two (methacrylic vinegar oxygen ethoxyl phenenyls), third hydrocarbon (bis (methacryloxyethoxyphenyl) propane) monomer to dissolve MPSMA, but the specific refractory power of two (methacrylic vinegar oxygen ethoxyl phenenyls), third hydrocarbon monomer is low, so need to use a large amount of MPSMA monomers, could promote the specific refractory power of polymeric composition; In addition, No. the 6541591st, United States Patent (USP), No. the 6953623rd, United States Patent (USP) etc. all utilizes the MPSMA monomer improving specific refractory power, but the MPSMA monomer costs an arm and a leg, and is unfavorable in industrial a large amount of uses.
Moreover, utilize interpolation nano inorganic particulate to improve specific refractory power, for example No. the 7282272nd, United States Patent (USP) discloses a kind of brightness enhancement film that improves its specific refractory power via adding the nano inorganic particulate, but the shortcoming of this method is a nanoparticle to be difficult for being dispersed in and to influence operation ease in the coating.
This shows that above-mentioned existing brightness enhancement film obviously still has inconvenience and defective, and demands urgently further being improved in structure and use.In order to solve the problem of above-mentioned existence, relevant manufacturer there's no one who doesn't or isn't seeks solution painstakingly, but do not see always that for a long time suitable design finished by development, and common product does not have appropriate structure to address the above problem, this obviously is the problem that the anxious desire of relevant dealer solves.Therefore how to found a kind of polymerisable compound and comprise the blooming of this polymerisable compound, real one of the current important research and development problem that belongs to, also becoming the current industry utmost point needs improved target.
In sum, the invention provides a kind of do not have above-mentioned shortcoming and easy to operate and comparatively economic high refractive index polymer coating, further improved the luminance gain value of brightness enhancement film.
Summary of the invention
Main purpose of the present invention is, overcomes the defective that existing brightness enhancement film exists, and a kind of new polymerisable compound is provided, and technical problem to be solved is to make it have high refractive index, is very suitable for practicality.
Another object of the present invention is to, overcome the defective that existing brightness enhancement film exists, and provide a kind of new blooming, technical problem to be solved be make its comprise a substrate and at least one deck by the formed coating of above-mentioned polymerisable compound, this blooming is used for the backlight module of indicating meter as brightness enhancement film, thereby is suitable for practicality more.
The object of the invention to solve the technical problems realizes by the following technical solutions.According to a kind of polymerisable compound that the present invention proposes, it comprises: (a) formula (I) monomer of 1 weight % to 90 weight %:
Figure G2009101788726D00021
Wherein, X 1Be H or methyl; X 2Be H or C 1-C 2Alkyl; X is O or S; R 1Be C 1-C 12The alkylene of straight or branched or inferior-oxyl; Reaching d and n is independently of one another for being selected from 0 to 3 integer; And (b) light trigger of 0.1 weight % to 10 weight %, based on the gross weight meter of polymerisable compound.
The object of the invention to solve the technical problems also can be applied to the following technical measures to achieve further.
Aforesaid polymerisable compound, wherein said (a) is formula (I 1) monomer
Figure G2009101788726D00022
Wherein, X 1Be H or methyl; R 1Be methylene radical, ethylidene, propylidene or isopropylidene; N is selected from 1 to 2 integer.
Aforesaid polymerisable compound, wherein said (a) is formula (I 2) monomer
Figure G2009101788726D00031
Aforesaid polymerisable compound, wherein in the gross weight of described polymerisable compound, the monomeric consumption of described formula (I) is 8 weight % to 70 weight %.
Aforesaid polymerisable compound, wherein in the gross weight of described polymerisable compound, the consumption of described light trigger is 1 weight % to 5 weight %.
The object of the invention to solve the technical problems also realizes by the following technical solutions.According to a kind of blooming that the present invention proposes, it comprises: substrate and at least one deck by the formed coating of polymerisable compound as the aforementioned.
The object of the invention to solve the technical problems also can be applied to the following technical measures to achieve further.
Aforesaid blooming, wherein said coating forms concentration structure.
The present invention compared with prior art has tangible advantage and beneficial effect.By technique scheme, the present invention has following advantage and beneficial effect at least: polymerisable compound of the present invention has at least 1.53 high refractive index, so have high refractive index by the prepared blooming of polymerisable compound of the present invention, this blooming can be used in the backlight module of indicating meter as brightness enhancement film, so that the good optical yield value to be provided; And, do not pollute the environment, so can effectively solve the existing problem of prior art because of not halogen-containing in the coating.In addition, polymerisable compound levelling property of the present invention is good, and the low advantage that possesses economically of cost.
The present invention has obvious improvement technically, and has tangible positively effect, really is a new and innovative, progressive, practical new design.
Above-mentioned explanation only is the general introduction of technical solution of the present invention, for can clearer understanding technique means of the present invention, and can be implemented according to the content of specification sheets, and for above-mentioned and other purposes, feature and advantage of the present invention can be become apparent, below especially exemplified by preferred embodiment, and conjunction with figs., be described in detail as follows.
Description of drawings
Fig. 1 is the synoptic diagram of an implementation method of blooming of the present invention.
Embodiment
Reach technique means and the effect that predetermined goal of the invention is taked for further setting forth the present invention, below in conjunction with accompanying drawing and preferred embodiment, polymerisable compound that foundation the present invention is proposed and its embodiment of blooming, structure, feature and the effect thereof that comprises this polymerisable compound, describe in detail as after.
Relevant aforementioned and other technology contents, characteristics and effect of the present invention can be known to present in the following detailed description that cooperates with reference to graphic preferred embodiment.By the explanation of embodiment, when can being to reach technique means that predetermined purpose takes and effect to obtain one more deeply and concrete understanding to the present invention, yet appended graphic only provide with reference to the usefulness of explanation, be not to be used for the present invention is limited.
Term used herein is not in order to restriction protection scope of the present invention only for describing described implementation method.Say it for example, employed term " " in the specification sheets, unless clear and definite explanation is arranged in the literary composition in addition, term " " is encompasses singular and most form.
In this article, " columnar structure " is made of two inclined surfaces, described inclined surface is plane or curved surface, and described two inclined surfaces form peak or arc in the prism roof intersection, and can be separately intersects in the bottom with another inclined surface of adjacent columnar structure and form paddy.
Particularly, the invention provides a kind of polymerisable compound, comprise:
(a) formula (I) monomer of 1 weight % to 90 weight %:
Figure G2009101788726D00041
Wherein,
X 1Be H or methyl; X 2Be H or C 1-C 2Alkyl;
X is O or S; R 1Be C 1-C 12The alkylene of straight or branched or inferior-oxyl; And
D and n are independently of one another for being selected from 0 to 3 integer; With
(b) light trigger of 0.1 weight % to 10 weight %,
Gross weight meter based on polymerisable compound.
Generally speaking, sulphur atom is because polarizability is higher, so specific refractory power is higher, and preferably, in formula (I) monomer, X is S, X 2Be H, and d is an integer 1.According to a specific embodiment of the present invention, described formula (I) monomer is tool formula (I 1) monomer:
Figure G2009101788726D00042
Wherein, R 1Be preferably methylene radical, ethylidene, propylidene or isopropylidene; N is selected from 1 to 2 integer; X 1Be H or methyl.
In better specific embodiment, be to use the R in formula (I) monomer 1Be ethylidene; N is 1; X 1Be H, that is, be following formula (I 2) monomer
Figure G2009101788726D00051
Above-mentioned formula (I) monomer has the high refractive index between 1.57~1.63, therefore can effectively increase the specific refractory power that described polymerisable compound solidifies back gained coating.Generally speaking, have high refractive index for making polymerisable compound, the monomeric consumption of formula (I) in the gross weight of described polymerisable compound, is at least 1 weight %, is preferably 8 weight % to 70 weight %, is more preferred from 30 weight % to 60 weight %.If the monomeric content of above-mentioned formula (I) is lower than 1 weight %, then polymerisable compound is difficult to have high refractive index, if surpass 90 weight %, then can cause polymerisable compound to solidify not exclusively, is unfavorable for coating.
Can be used for the light trigger (composition (b)) in the polymerisable compound of the present invention, be after rayed, can produce free radical, and the transmission by free radical and the compound of initiated polymerization, it for example can be selected from following group: benzophenone (benzophenone), st-yrax (benzoin), benzil (benzil), 2,2-dimethoxy-1,2-phenylbenzene second-1-ketone (2,2-dimethoxy-1,2-diphenylethan-1-one), 1-hydroxycyclohexylphenylketone (1-hydroxy cyclohexyl phenyl ketone), 2,4,6-Three methyl Benzene first anilide diphenyl phosphine oxide (2,4,6-trimethylbenzoyl diphenyl phosphine oxide; TPO) and combination, benzophenone preferably.
Light trigger consumption of the present invention there is no particular restriction, can adjust according to the kind and the consumption thereof of the polymerisable monomer that described polymerisable compound comprised.Generally speaking, in the gross weight of described polymerisable compound, be 0.1 weight % to 10 weight %, be preferably 1 weight % to 5 weight %.
For increasing the reactivity of polymerisable compound, and after it solidifies, has good thermotolerance, and can keep high refractive index, the present composition optionally adds (c) other monomer, and for keeping polymerisable compound high refractive index characteristic of the present invention, (c) other monomeric specific refractory power is good to be not less than 1.6, for example formula (II) monomer
Figure G2009101788726D00052
Wherein,
X 3And X 4Be to be H or C independently of one another 1-C 4Alkyl preferably is H or methyl independently of one another;
Y 1, Y 2, Y 3And Y 4Be to be H, C independently of one another 1-C 4Alkyl or OH preferably are H or methyl independently of one another; And
A and b are independently of one another for being selected from 0 to 5 integer, preferably independently of one another for being selected from 1 to 3 integer
Preferably, in formula (II) monomer, X 3, X 4, Y 1, Y 2, Y 3And Y 4Be independently of one another for H or methyl, and a and b are independently of one another for being selected from 1 to 3 integer.
According to a specific embodiment of the present invention, described formula (II) monomer is concrete formula (II 1) monomer:
Figure G2009101788726D00061
If when adding, other monomeric consumption of composition (c) in the gross weight of described polymerisable compound, is preferably 1 weight % to 50 weight %, is more preferred from 5 weight % to 40 weight %, the best is 15 weight % to 30 weight %.Generally speaking, when the monomeric consumption of formula (II) during less than 1 weight %, polymerisable compound can't reach thermostability; When the monomeric consumption of formula (II) during greater than 50 weight %, the polymerisable compound viscosity of gained is too big, is unfavorable for coating.
General polymerisable compound all can add some multiple functional radical monomers or oligopolymer as linking agent (Crosslinking agent), to increase molecule and intermolecular degree of crosslinking when the polymerization, makes composition be easy to solidify, and can promote solidify after the hardness of coating.Polymerisable compound of the present invention optionally adds (d) linking agent, to promote the film-forming properties of polymerisable compound of the present invention.According to of the present invention one preferred implementation method, add oligopolymer in the polymerisable compound of the present invention as linking agent, solidify the formed coating hardness in back to increase molecule and intermolecular degree of crosslinking and to increase described polymerisable compound, make coating hardness reach pendulum hardness (pendulum hardness) more than 50 or 50, but when pendulum hardness greater than 80 the time, embrittlement easily is so preferred pendulum hardness is 50 to 80.The kind of above-mentioned linking agent is that to have the technician of common knowledge in the technical field of the invention known, such as but not limited to acrylate, the aforesaid propylene acid esters can have one or more functional group, preferably has multiple functional radical, can be used for acrylate among the present invention such as but not limited to (methyl) acrylate, as tripropylene glycol two (methyl) acrylate (tripropylene glycol di (meth) acrylate), 1,4-butyleneglycol two (methyl) acrylate (1,4-butanediol di (meth) acrylate), 1,6-hexylene glycol two (methyl) acrylate (1,6-hexanediol di (meth) acrylate), polyoxyethylene glycol two (methyl) acrylate (polyethyleneglycol di (meth) acrylate), allylation two (methyl) cyclohexyl acrylate (allylated cyclohexyl di (meth) acrylate), isocyanuric acid ester two (methyl) acrylate (isocyanurate di (meth) acrylate), ethoxylation trishydroxymethyl third hydrocarbon three (methyl) acrylate (ethoxylated trimethylolpropane tri (meth) acrylate), propoxylated glycerol three (methyl) acrylate (propoxylated glycerol tri (meth) acrylate), trishydroxymethyl third hydrocarbon three (methyl) acrylate (trimethylol propane tri (meth) acrylate), three (propylene vinegar oxygen ethyl) cyamelide (tris (acryloxyethyl) isocyanurate); Urethane acrylate (urethane acrylate) is as aliphatic carbamate acrylate (aliphaticurethane acrylate) or aromatic amino ester formate acrylate (aromatic urethaneacrylate); Polyester acrylate (polyester acrylate) is as polyester diacrylate (polyester diacrylate); Epoxy acrylate (epoxy acrylate) is as bisphenol-A epoxy diacrylate (bisphenol-A epoxy diacrylate), phenolic aldehyde epoxy acrylate (novolac epoxy acrylate); Or its mixture.Be preferably urethane acrylate or epoxy acrylate or its mixture.
The commercial acrylate oligopolymer example that can be used for composition of the present invention (d) comprises:
(methyl) origoester acrylate: EBECRYL-745 (excellent happiness green (UCB) limited-liability company system); DOUBLEMER3778, DOUBLEMER1701, DOUBLEMER345, DOUBLEMER1703, DOUBLEMER530, DOUBLEMER570, DOUBLEMER236 and DOUBLEMER584 (two key chemical industry company limited system); 6530B-40,6531B-40,6532B-40 and 6533B-40 (Changxing chemical industry system).
Aliphatic poly urethane acrylate oligomer: 6101-100,611A-85,611B-85,6112-100,6113,6114,6115J-80,6130B-80,6131-1,6134B-80,6141H-80,6143A-80,6143C-60,6144-100,6145-100,6145-100H, 6148J-75,6148T-85,6149-100,615-100,6150-100,6151,6152B-80,6154B-80,6157B-80,6158B-80,6160B-70,6161-100,6181 and 6196-100 (Changxing (Eternal) chemical industry system); AgiSyn TM230T1 and AgiSyn TM230A2 (Xin Limei science and technology (thigh) corporate system); EBECRYL-264, EBECRYL-4820, EBECRYL-270, EBECRYL-230, EBECRYL-284 and EBECRYL-1290 (excellent happiness green (UCB) limited-liability company system); HENKEL 6010 (peaceful (COGNIS) corporate system of section); CN9001, CN9002, CN9004 and CN9006 (Sartomer (Sartomer) corporate system);
Figure G2009101788726D00071
U100,
Figure G2009101788726D00072
VP LS 2265, VP LS2308,
Figure G2009101788726D00074
U375H,
Figure G2009101788726D00075
VP LS 2220,
Figure G2009101788726D00076
XP2491,
Figure G2009101788726D00077
XP 2513,
Figure G2009101788726D00078
U200 reaches
Figure G2009101788726D00079
XP 2609 (Bayer (Bayer) corporate system).
Aromatic series polyurethane(s) origoester acrylate: 6120F-80,6121F-80,6122F-80 and 6146-100 (Changxing chemical industry system); 670T1, AgiSyn TM670A2 (Xin Limei science and technology (thigh) corporate system); EBECRYL-204, EBECRYL-205, EBECRYL-210, EBECRYL-215, EBECRYL-220 and EBECRYL-6202 (excellent happiness green (UCB) limited-liability company system).
Polyester acrylic ester oligomer: EBECRYL-830 and EBECRYL-524 (excellent happiness green (UCB) limited-liability company system); 6315,6320,6323-100,6325-100,6327-100,6336-100 and 6361-100 (Changxing chemical industry system).
Epoxy acrylate oligomer: AgiSyn TM1010, AgiSyn TM1010A80, AgiSyn TM1010B80, AgiSyn TM1010C80 (Xin Limei science and technology (thigh) corporate system); 621,622,623-100,6210G, 624-100,6231,6241,6213-100,6215-100,625,6261 and 620-100 (Changxing chemical industry system); EBECRYL-600, EBECRYL-605, EBECRYL-648, EBECRYL-1608, EBECRYL-3105, EBECRYL-3416, EBECRYL-3700, EBECRYL-3701, EBECRYL-3703, EBECRYL-3708 and EBECRYL-6040 (excellent happiness green (UCB) limited-liability company system).
If when adding, the consumption of composition (d) linking agent in the gross weight of described polymerisable compound, can be 1 weight % to 60 weight %, is preferably 10 weight % to 50 weight %, is more preferred from 20 weight % to 45 weight %.
In addition, the present composition optionally adds any known additive except that above-mentioned possible composition, to change its physics or chemical property.Can be used for additive of the present invention and generally can be selected from following group: thinner, mineral filler, static inhibitor, lubrication prescription (slip agent), tensio-active agent, flow agent (leveling agents), defoamer and combination thereof.
The viscosity of polymerisable compound is to change with factors such as ingredient, content, service temperatures in the described composition.According to the present invention, optionally in described polymerisable compound, add thinner, to adjust the viscosity of polymerisable compound, above-mentioned thinner is preferably acrylic ester monomer, the thinner that is suitable for for example but is not limited to be selected from following group: (methyl) acrylate, 2-phenoxyethyl acrylate (2-phenoxyl ethyl acrylate), 2-(2-ethoxy ethoxy) ethyl propylene acid esters (2-(2-ethoxyethoxy) ethyl acrylate), the trishydroxymethyl third hydrocarbon triacrylate (trimethylolpropane triacrylate), polyethyleneglycol diacrylate (polyethyleneglycol diacrylate), polyoxyethylene glycol neighbour-phenyl ether acrylate (Polyethyleneglycol o-phenylphenyl ether acrylate), cumyl phenoxyethyl acrylate (cumyl phenoxyl ethyl acrylate), vinylformic acid xenyl epoxy ethyl ester (biphenylepoxyethyl acrylate), bisphenol-A epoxy diacrylate (bisphenol-Aepoxy diacrylate), phenolic aldehyde epoxy acrylate (novolac epoxy acrylate) the third oxidation neopentylglycol diacrylate (propoxylated neopentyl glycol diacrylate), the ethoxyquin trishydroxymethyl third hydrocarbon triacrylate (ethoxylated trimethylolpropanetriacrylate), the third oxidation trishydroxymethyl, the third hydrocarbon triacrylate (propoxylatedtrimethyloipropane triacrylate), two new penta tetrol, six acrylate (dipentaerythritol hexaacrylate DPHA) and these combinations.Commercially available this type of monomeric example comprises: produced by Sartomer (Sartomer) company, commodity are by name
Figure G2009101788726D00081
Figure G2009101788726D00082
Or The person; Produced by Changxing (Eternal) company, commodity are by name
Figure G2009101788726D00084
The person.
For promoting the hardness of the formed coating in composition curing back, optionally in composition, add mineral filler, to avoid influencing optical property because of the concentration structure collapse phenomenon.In addition, mineral filler also has the effect of the briliancy that promotes panel of LCD.Can be used in mineral filler of the present invention and be that to have the technician of common knowledge in the technical field of the invention known, it is preferably titanium dioxide, zirconium white, silicon-dioxide, zinc oxide or its mixture such as but not limited to zinc oxide, silicon-dioxide, strontium titanate, zirconium white, aluminum oxide, lime carbonate, titanium dioxide, calcium sulfate, barium sulfate or its mixture.Above-mentioned mineral filler has the size of about 10 nanometers to about 350 nanometers, is preferably 50 nanometer to 150 nanometers.
Optionally add static inhibitor in polymerisable compound, make it have anlistatig effect, and then improve the operation yield.It is known to be used in static inhibitor of the present invention and to be the technician who has common knowledge in the technical field of the invention, and it is such as but not limited to oxyethyl group glycerol fatty acid ester class, quaternary ammonium compound, aliphatic amide analog derivative, Resins, epoxy (as poly-epoxy second hydrocarbon), silica hydrocarbon (siloxane) or other alcohol derivatives (as poly-ethanol ester or polyglycol ether) etc.
Polymerisable compound of the present invention can be coated on a substrate or the otpical leaf (Optical thinsheet) (for example any known diffusion barrier or condensing film), be used to form the coating of a blooming, described coating has concentration structure, can increase surface abrasion resistance (wear resistance) and superior slickness (smoothness) is provided; And because of polymerisable compound of the present invention comprises formula (I) monomer with high refractive index, so can make formed coating have high refractive index.The specific refractory power of coating of the present invention is at least 1.53, is preferably 1.57 to 1.63, can effectively promote the briliancy of otpical leaf.
The material of aforesaid substrate can be any the technical field of the invention, and to have a technician of common knowledge known, for example glass or plastics.Above-mentioned plastic base can be made of one or more polymer resins layers.Kind in order to the resin that constitutes above-mentioned polymer resins layers there is no particular restriction, it for example is selected from following group: vibrin (polyester resin), as polyethylene terephthalate (polyethylene terephthalate, PET) or Polyethylene Naphthalate (polyethylenenaphthalate, PEN), polyacrylate resin (polyacrylate resin), as polymethylmethacrylate (polymethyl methacrylate, PMMA), polyolefin resin (polyolefinresin), as polyethylene (PE) or polypropylene (PP), poly-cyclic olefin resins (polycycloolefinresin), polyimide resin (polyimide resin), polycarbonate resin (polycarbonateresin), polyurethane resin (polyurethane resin), cellulosetri-acetate (triacetyl cellulose, TAC), poly(lactic acid) (Polylactic acid) and combination thereof, but not as limit.Wherein, preferably be selected from vibrin, polycarbonate resin and combination thereof; It more preferably is polyethylene terephthalate.The thickness of substrate depend on usually the demand of the optical articles desiring to make, be generally 30 microns to 300 microns.
The present invention provides a kind of blooming in addition, its comprise a substrate and at least one deck by the formed coating of above-mentioned polymerisable compound.Blooming of the present invention can be used in the backlight module of indicating meter as brightness enhancement film (brightness enhancement film).
Fig. 1 is the synoptic diagram of an implementation method of blooming of the present invention.As shown in Figure 1, blooming of the present invention comprises the coating 2 that a substrate 1 and is concentration structure.
The coat-thickness of blooming of the present invention is generally 1 micron to 100 microns, is preferably 10 microns to 40 microns, and the best is 15 microns to 25 microns.When coating had the form of ad hoc structure, coat-thickness was the vertex calculating with its structure.Blooming with Fig. 1 is an example, and the thickness of coating 2 is shown in symbol a.
According to an implementation method of the present invention, described coating has concentration structure.The concentration structure of blooming of the present invention is known for the technician who has common knowledge in the technical field of the invention, its such as but not limited to: regular or irregular prism columnar structure is (promptly, the triangle column), the arc columnar structure (promptly, the peak of columnar structure is arc form), lentoid and capsule shape structure or its combination etc., be preferably prism columnar structure or arc columnar structure or its combination.Above-mentioned prism columnar structure and/or arc columnar structure can be linearity (linear), broken-line type (zigzag) or shaped form (serpentine), are preferably the linear prism columnar structure.And two adjacent columnar structures can be parallel or not parallel.For reducing the optical interference phenomenon, concentration structure layer of the present invention can comprise plural at least uneven each other columnar structure, and above-mentioned columnar structure can be prism columnar structure or arc columnar structure or its combination, is preferably the prism columnar structure.According to the present invention, described concentration structure layer comprises at least one group of uneven two prism columnar structures that intersected and/or at least one group of uneven two prism columnar structures that do not intersect.
Blooming of the present invention can anyly have the known mode of technician of common knowledge in the technical field of the invention and make.For example, can be via the method manufacturing that comprises following steps:
(1) mixes the monomer, light trigger of tool formula (I) and monomer, linking agent and other additive of optional tool formula (II), to form a colloidal state polymerisable compound;
(2) the colloidal state polymerisable compound of step (1) gained is coated on the substrate by rights, formed a coating, utilize for example roller embossing on coating, to form a concentration structure again; And
(3) solidify above-mentioned coating, this can reach its irradiation energy ray for example under normal temperature or heating.
Optionally, can repeat above steps, to obtain to comprise the blooming of a plurality of coatings.
For avoiding the substrate surface scratch to influence the diaphragm-operated optical property, optionally substrate with respect to another surface by the formed coating of polymerisable compound of the present invention on forms one anti-scratch layer.Above-mentioned anti-scratch layer can be level and smooth shape or non-level and smooth shape.The thickness of above-mentioned anti-scratch layer is preferably between the 0.5-30 micron, measures according to JIS K7136 standard method, and gained mist degree (Haze) is 1%-90%, is preferably 5%-40%.According to JIS K7136 standard method, measure the total light transmittance (Total Light Transmittance) of blooming of the present invention, blooming of the present invention has and is not less than 60% total light transmittance, is preferably to be higher than 80%, is more preferred from more than 90% or 90%.
Polymerisable compound of the present invention has at least 1.53 high refractive index, so have high refractive index by the prepared blooming of polymerisable compound of the present invention, this blooming can be used in the backlight module of indicating meter as brightness enhancement film, so that the good optical yield value to be provided; And, do not pollute the environment, so can effectively solve the existing problem of prior art because of not halogen-containing in the coating.In addition, polymerisable compound levelling property of the present invention is good, and the low advantage that possesses economically of cost.
Following examples will be at the invention provides further instruction.
Embodiment 1-6
Prepare the blooming of embodiment 1 to 6 according to mode described below, the combination of each Example formulations is listed as table 1.
At first, each component is mixed with the listed part by weight of table 1, under 50 ℃ temperature, with rotating speed 1,000rpm stirs, and forms a colloidal state polymerisable compound again.
This colloidal state polymerisable compound is coated (model on polyphenyl dioctyl phthalate second diester (PET) substrate
Figure G2009101788726D00111
East beautiful (TORAY) company produces), to form coating, utilize roller embossing mode on coating, to form a prism decorative pattern then.Then, at normal temperatures, shine described coating, make its curing with energy-ray.Obtain having the blooming that thickness is 25 microns coating.
Table 1
Figure G2009101788726D00112
(a): formula (I) monomer (Sigma's aldrich (Sigma-Aldrich) company produces, 2-(naphthyl-7-sulfo-) ethyl propenoate (2-(naphthalen-7-ylthio) ethyl acrylate))
(b): light trigger (vapour Bagong department produces,
Figure G2009101788726D00113
)
(d): (Changxing company produces linking agent, 623-
Figure G2009101788726D00114
)
Specific refractory power test (automatic refractometer (AUTOMATIC REFRACTOMETER) GPR11-that uses index instrument (IndexInstruments) company to provide is provided the blooming of the various embodiments described above
Figure G2009101788726D00115
Instrument), and each described blooming is applied to Benq (BenQ) 22 inches side type backlight modules that company provided, (BM-that Pu Kang (TOPCON) company provides is opened up in employing to carry out the test of luminance gain degree
Figure G2009101788726D00116
Instrument), the gained result is as shown in table 2.
Table 2
Embodiment Specific refractory power The luminance gain degree
??1 ??1.550 ??68.5%
??2 ??1.553 ??69.8%
??3 ??1.561 ??71.1%
??4 ??1.566 ??72.6%
??5 ??1.571 ??73.0%
??6 ??1.575 ??73.8%
By the result of embodiment in the table 21 to 6 as can be known, the specific refractory power of the formed coating of polymerisable compound of the present invention all is higher than 1.55, and the coating specific refractory power is higher, and when being applied to backlight module, its luminance gain degree is higher, and preferred spotlight effect can be provided.
Embodiment 7-10
Repeat the preparation method of the blooming of embodiment 1 to 6.
The combination of embodiment 7-10 prescription is listed as table 3.
Table 3
(a): formula (I) monomer (Aldrich produces)
(b): light trigger (vapour Bagong department produces,
Figure G2009101788726D00122
)
(c): (Xin Zhong village company produces other monomer, A-BPEF)
(d): (Changxing company produces linking agent, 623-
Figure G2009101788726D00123
)
The blooming of the foregoing description 6-10 is carried out heat stability test (using thermal gravimetric analyzer Shimadzu TGA-50H), the thermostability of the blooming of the embodiment 6-10 that is obtained, the gained result is as shown in table 4.
Table 4
Embodiment 6 samples Temperature (℃) ??315.0
Weightless (%) ??-5
Embodiment 6 samples Temperature (℃) ??315.0
Embodiment 7 samples Temperature (℃) ??323.3
Weightless (%) ??-5
Embodiment 8 samples Temperature (℃) ??332.1
Weightless (%) ??-5
Embodiment 9 samples Temperature (℃) ??342.3
Weightless (%) ??-5
Embodiment 10 samples Temperature (℃) ??354.6
Weightless (%) ??-5
By the listed result of table 4 as seen, polymerisable compound of the present invention adds (c) other monomer, and behind its film-forming, cured film has thermostability preferably.
Comparative example 1-2
Formula (I) monomer is replaced as (a ') monomer or (a ") monomer, repeats the preparation method of the blooming of embodiment 1, the combination of comparative example 1-2 prescription is listed as table 5
Table 5
Figure G2009101788726D00131
(a '): (Changxing company produces monomer, EM210)
(a "): (Changxing company produces monomer, EM2108)
(b): light trigger (vapour Bagong department produces,
Figure G2009101788726D00132
)
(d): (Changxing company produces linking agent, 623-
Figure G2009101788726D00133
)
Specific refractory power test (the AUTOMATIC REFRACTOMETER GPR11-that uses Index Instruments company to provide is provided the blooming of above-mentioned each comparative example
Figure G2009101788726D00134
Instrument), and each described blooming is applied to 22 inches side type backlight modules that BenQ company is provided, the luminance gain degree test (BM-that adopts TOPCON company to provide is provided
Figure G2009101788726D00135
Instrument), the gained result is as shown in table 6.
Table 6
Comparative example Index of refraction The luminance gain degree
??1 ??1.529 ??63.4%
??2 ??1.533 ??64.8%
According to the result of table 6 as can be known, be compared to the composition of embodiment 1, the composition of comparative example 1 or comparative example 2, because of not containing formula (I) monomer, so specific refractory power is lower, the luminance gain effect is relatively poor.
The above, it only is preferred embodiment of the present invention, be not that the present invention is done any pro forma restriction, though the present invention discloses as above with preferred embodiment, yet be not in order to limit the present invention, any those skilled in the art, in not breaking away from the technical solution of the present invention scope, when the technology contents that can utilize above-mentioned announcement is made a little change or is modified to the equivalent embodiment of equivalent variations, in every case be not break away from the technical solution of the present invention content, according to technical spirit of the present invention to any simple modification that above embodiment did, equivalent variations and modification all still belong in the scope of technical solution of the present invention.

Claims (13)

1. polymerisable compound is characterized in that it comprises:
(a) formula (I) monomer of 1 weight % to 90 weight %:
Figure F2009101788726C00011
Wherein,
X 1Be H or methyl; X 2Be H or C 1-C 2Alkyl;
X is O or S; R 1Be C 1-C 12The alkylene of straight or branched or inferior-oxyl; And
D and n are independently of one another for being selected from 0 to 3 integer; And
(b) light trigger of 0.1 weight % to 10 weight % is based on the gross weight meter of polymerisable compound.
2. polymerisable compound according to claim 1 is characterized in that wherein said (a) is formula (I 1) monomer
Figure F2009101788726C00012
Wherein, X 1Be H or methyl; R 1Be methylene radical, ethylidene, propylidene or isopropylidene; N is selected from 1 to 2 integer.
3. polymerisable compound according to claim 1 is characterized in that wherein said (a) is formula (I 2) monomer
4. polymerisable compound according to claim 1 is characterized in that wherein in the gross weight of described polymerisable compound, the monomeric consumption of described formula (I) is 8 weight % to 70 weight %.
5. polymerisable compound according to claim 1 is characterized in that wherein in the gross weight of described polymerisable compound, the consumption of described light trigger is 1 weight % to 5 weight %.
6. polymerisable compound according to claim 1 is characterized in that further comprising (c) other monomer.
7. polymerisable compound according to claim 6 is characterized in that wherein said (c) other monomeric specific refractory power is not less than 1.6.
8. polymerisable compound according to claim 6 is characterized in that wherein said (c) is formula (II) monomer
Figure F2009101788726C00021
Wherein,
X 3And X 4Be to be H or methyl independently of one another;
Y 1, Y 2, Y 3And Y 4Be to be H, C independently of one another 1-C 2Alkyl or OH; And
A and b are independently of one another for being selected from 0 to 3 integer.
9. polymerisable compound according to claim 8 is characterized in that wherein said (c) is formula (II 1) monomer:
Figure F2009101788726C00022
10. polymerisable compound according to claim 1 is characterized in that further comprising (d) linking agent.
11. polymerisable compound according to claim 10 is characterized in that wherein said linking agent is (methyl) acrylate, urethane acrylate, polyester acrylate, epoxy acrylate or its combination.
12. a blooming is characterized in that it comprises: substrate and at least one deck by the formed coating of polymerisable compound as claimed in claim 1.
13. blooming according to claim 12 is characterized in that wherein said coating forms concentration structure.
CN200910178872A 2009-10-09 2009-10-09 Polymerizable composition and optical film comprising same Pending CN101792500A (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102485808A (en) * 2010-12-02 2012-06-06 比亚迪股份有限公司 Polymerizable composition, backlight module and liquid crystal display
CN105705580A (en) * 2013-10-07 2016-06-22 三菱瓦斯化学株式会社 (Meth)acrylic copolymer, resin composition, and molded product of said resin composition
TWI577733B (en) * 2012-11-28 2017-04-11 Riken Technos Corp Active energy ray hardening resin composition
US10138372B2 (en) 2015-02-05 2018-11-27 Mitsubishi Gas Chemical Company, Inc. Polycarbonate resin composition and article molded therefrom

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102485808A (en) * 2010-12-02 2012-06-06 比亚迪股份有限公司 Polymerizable composition, backlight module and liquid crystal display
CN102485808B (en) * 2010-12-02 2014-12-10 比亚迪股份有限公司 Polymerizable composition, backlight module and liquid crystal display
TWI577733B (en) * 2012-11-28 2017-04-11 Riken Technos Corp Active energy ray hardening resin composition
CN105705580A (en) * 2013-10-07 2016-06-22 三菱瓦斯化学株式会社 (Meth)acrylic copolymer, resin composition, and molded product of said resin composition
CN105705580B (en) * 2013-10-07 2018-07-20 三菱瓦斯化学株式会社 (methyl) acrylic copolymer, resin combination and its formed body
US10081729B2 (en) 2013-10-07 2018-09-25 Mitsubishi Gas Chemical Company, Inc. (Meth)acrylic copolymer, resin composition, and molded product of said resin composition
US10731033B2 (en) 2013-10-07 2020-08-04 Mitsubishi Gas Chemical Company, Inc. (Meth)acrylic copolymer, resin composition, and molded product of said resin composition
US10138372B2 (en) 2015-02-05 2018-11-27 Mitsubishi Gas Chemical Company, Inc. Polycarbonate resin composition and article molded therefrom

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