WO2006046481A1 - Optical methacrylic resin extrusion plate manufacturing method - Google Patents

Optical methacrylic resin extrusion plate manufacturing method Download PDF

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Publication number
WO2006046481A1
WO2006046481A1 PCT/JP2005/019390 JP2005019390W WO2006046481A1 WO 2006046481 A1 WO2006046481 A1 WO 2006046481A1 JP 2005019390 W JP2005019390 W JP 2005019390W WO 2006046481 A1 WO2006046481 A1 WO 2006046481A1
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Prior art keywords
methacrylic resin
plate
polymer
polymerization
apparent density
Prior art date
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PCT/JP2005/019390
Other languages
French (fr)
Japanese (ja)
Inventor
Shunji Kamiya
Yoshikazu Tsuruta
Original Assignee
Asahi Kasei Chemicals Corporation
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Publication date
Application filed by Asahi Kasei Chemicals Corporation filed Critical Asahi Kasei Chemicals Corporation
Priority to CN200580034052XA priority Critical patent/CN101035665B/en
Priority to JP2006543090A priority patent/JP4717008B2/en
Publication of WO2006046481A1 publication Critical patent/WO2006046481A1/en

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Classifications

    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B6/00Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings
    • G02B6/0001Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings specially adapted for lighting devices or systems
    • G02B6/0011Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings specially adapted for lighting devices or systems the light guides being planar or of plate-like form
    • G02B6/0065Manufacturing aspects; Material aspects
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/18Manufacture of films or sheets
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L33/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • C08L33/04Homopolymers or copolymers of esters
    • C08L33/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
    • C08L33/10Homopolymers or copolymers of methacrylic acid esters
    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/13Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on liquid crystals, e.g. single liquid crystal display cells
    • G02F1/133Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
    • G02F1/1333Constructional arrangements; Manufacturing methods
    • G02F1/1335Structural association of cells with optical devices, e.g. polarisers or reflectors
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/03Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
    • B29C48/07Flat, e.g. panels
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2333/00Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
    • C08J2333/04Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters
    • C08J2333/06Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters of esters containing only carbon, hydrogen, and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C08J2333/10Homopolymers or copolymers of methacrylic acid esters
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/02Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/14Polymer mixtures characterised by other features containing polymeric additives characterised by shape
    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/13Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on liquid crystals, e.g. single liquid crystal display cells
    • G02F1/133Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
    • G02F1/1333Constructional arrangements; Manufacturing methods
    • G02F1/1335Structural association of cells with optical devices, e.g. polarisers or reflectors
    • G02F1/1336Illuminating devices
    • G02F1/133615Edge-illuminating devices, i.e. illuminating from the side

Definitions

  • the present invention is used for office automation equipment such as personal computers and word processors, various monitors for displaying image signals, for example, display devices used for panel monitors, television monitors and the like, and surface light source devices for indoor and outdoor spaces.
  • the present invention relates to a method for producing a methacrylic resin extruded plate for a light guide plate suitable for a display device or a signboard.
  • Transparent thermoplastic resin and in particular, methallyl resin, in particular, has been used for many lighting applications because of its excellent light transmission and mechanical properties. It has come to be used as a light guide plate for backlights of display devices.
  • backlight systems There are two commonly used backlight systems: the so-called direct type, in which the light guide plate is sandwiched between the light source and the liquid crystal unit, and the edge light method in which the light source is attached to the edge of the light guide plate. The method has become mainstream.
  • development has continued under the concept of brighter, larger and thinner products, where the demand for higher brightness, larger size, and thinner display devices is stronger.
  • the light guide plate used in the light source device also has a great demand for a light guide plate that efficiently emits incident light of light incident from the light source lamp disposed on the side surface to the output surface. It is getting stronger.
  • a number of technical disclosures have been made so far regarding the method of increasing the brightness using the light guide plate.
  • a method of obtaining a uniform light emitting surface by dispersing and diffusing light diffusing particles in a light guide plate see, for example, Patent Document 1
  • a light scattering plastic material including fine particles having different refractive indexes in a light guide is disclosed.
  • Patent Document 2 the process is complicated.
  • Patent Document 1 Japanese Patent Publication No. 39-1194
  • Patent Document 2 JP-A-4-145485
  • the level can sufficiently meet the demands associated with the increase in size and thickness of display devices, such as brightness and luminance spots. It is the current situation that has been reached.
  • An object of the present invention is suitable for various monitors that display image signals, for example, display devices used for panel monitors, television monitors and the like, and display devices and signboards used for indoor and outdoor lighting devices.
  • An object is to provide a methacrylic resin extruded plate for a light guide plate and a method for producing the same.
  • the present inventors mixed a metataryl resin extruded material having an irregular shape with a metataryl resin extruded material having a fixed shape at a specific ratio, and then extrusion molding.
  • methacrylic resin plate used as a light guide plate it was found that the brightness was increased and the brightness unevenness was reduced, and the present invention was completed.
  • the apparent density between the apparent density methacrylic resin having an apparent density of 0.63 gZml to 0.78 gZml and the amorphous methacrylic resin polymer having an apparent density of 0.55 gZml to 0.63 gZml is at least 0.80 gZml.
  • the resulting mixture is extruded, and the thickness is 2.0-15. Omm, and the thickness accuracy in the width direction is within ⁇ 1.0% of the average thickness.
  • the methacrylic resin used in the present invention is methyl methacrylate!
  • the / soot can be obtained by copolymerizing 70% by weight or more of methacrylic acid methacrylate and a monomer having copolymerizability with these.
  • Monomers that are copolymerizable with these include butyl methacrylate, ethyl methacrylate, methyl methacrylate, propyl methacrylate, cyclohexyl methacrylate, methacrylate methacrylate, 2-ethylhexyl methacrylate, etc.
  • Methacrylic acid esters Methyl acrylate, Ethyl acrylate, Butyl acrylate, Acrylic acid cyclohexyl, Acrylic acid ester, Acrylic acid ester such as 2-Ethylhexyl acrylate, Methacrylic acid, Acrylic
  • the power of unsaturated acids such as acids is not limited to these.
  • the regular-shaped methacrylic resin extruded raw material used in the present invention is a spherical, cylindrical or flat methacrylic resin obtained by a polymerization reaction.
  • the unshaped metataryl resin extrusion raw material is methacrylic resin obtained by mechanically crushing a methacrylic resin molding once formed into a plate shape.
  • the spherical methacrylic resin is obtained by a suspension polymerization method.
  • the suspension polymerization method will be described.
  • a polymerization initiator and a chain transfer agent are uniformly dissolved in a monomer mixture consisting of methyl methacrylate or ethyl methacrylate and another monomer.
  • the homogeneously dissolved product is suspended in an aqueous medium containing a dispersion stabilizer and then held at a predetermined polymerization temperature for a certain period of time to complete the polymerization.
  • the resulting turbid polymer is filtered, washed with water and dried. Is obtained.
  • the polymerization initiator used in suspension polymerization may be a radical polymerization initiator known for polymerization of vinyl monomers.
  • azobisisobutyrate-tolyl 2,2 'azobis (2,4 dimethylvale-tolyl), dimethyl-2,2, -azobisisobutyrate, tert-butylperoxypivalate, tert-butylperoxy 2-
  • examples include ethyl hexaate, cumyl paroxy 2-ethyl hexanoate, benzoyl peroxide, lauroyl peroxide, and the like.
  • These radical polymerization initiators are preferably used in an amount of usually 0.01 to 2.0 parts by weight per 100 parts by weight of the monomer or monomer mixture.
  • the chain transfer agent used in the suspension polymerization may be a well-known one used for polymerization of methyl methacrylate.
  • t-butyl mercaptan examples thereof include n-octyl mercaptan and n-dodecyl mercaptan.
  • the amount of these chain transfer agents used is usually preferably in the range of 0.01 to 2.0 parts by weight per 100 parts by weight of the monomer or monomer mixture.
  • the dispersion stabilizer used in the suspension polymerization is not particularly limited. However, it is a poorly water-soluble inorganic compound such as calcium phosphate, calcium carbonate, and aluminum hydroxide, polybutal alcohol, polyethylene oxide, and cellulose derivative. -On-based polymer compounds, polyacrylic acid and its salts, polymethacrylic acid and its salts, copolymer of methacrylic acid ester and methacrylic acid and its salts, etc. .
  • the amount of these dispersion stabilizers used is preferably in the range of 0.01 to 5.0 parts by weight per 100 parts by weight of water.
  • water used in the suspension polymerization examples include pure water, ion exchange water, and deionized water.
  • the amount of water used is not particularly limited, but is preferably in the range of 100 to 250 parts by weight per 100 parts by weight of the monomer or monomer mixture! /.
  • the polymerization temperature for suspension polymerization is not particularly limited, but is about 60 to 120 ° C and is suitable for the polymerization initiator used.
  • a polymerization apparatus a polymerization vessel equipped with a well-known stirring blade, for example, a turbine blade, a fiddler blade, a propeller blade, a blue margin blade, or the like, is used, and the vessel is provided with a kaffle. Is common.
  • a release agent, a colorant, an ultraviolet absorber, an antioxidant, a light diffusing agent, a plasticizer, etc. may be suspended and polymerized.
  • the spherical methacrylate resin can be obtained by washing, dehydrating and drying by a known method.
  • the average particle size of the spherical methallyl succinic polymer which is an important constituent of the present invention, is 0.2 to 0.5 mm, preferably 0.25 to 0.39 mm. Good plate thickness accuracy can be obtained when the thickness is 0.2 mm or more, and a polymer having an average particle diameter of 0.5 mm or less can be stably produced. Further, when the apparent density is in the range of 0.70 g / ml to 0.78 g / ml, good thickness accuracy can be obtained.
  • Cylindrical methacrylic resin is a spherical polymer obtained by suspension polymerization.
  • Tacryl resin can be supplied to an extruder equipped with a vent, extruded at a temperature of 220 to 260 ° C and vented vacuum pressure of 1.3 to 8 kPa in a strand from an extrusion die, water cooled, and cut with a strand cutter.
  • a molten methacrylic resin polymer obtained by a known solution polymerization method or bulk polymerization method can be extruded into a strand shape from an extrusion die, cooled with water, and cut with a strand cutter.
  • the flat methacrylic resin can be extruded from an extruder with a vent in the same manner as in the production of the cylindrical methacrylic resin, and then cut with an underwater cutter.
  • the solvent in the solution polymerization method has a higher boiling point than the methyl methacrylate monomer, the methyl methacrylate monomer, and the monomer copolymerizable with methyl methacrylate at the bottom and inside of the distillation column.
  • aromatic compounds such as toluene, xylene, ethylbenzene, and jetylbenzene, aliphatic compounds such as octane and decane, alicyclic compounds such as decalin, esters such as butyl acetate and pentyl acetate, 1, And halogen compounds such as 1, 2, 2-tetrachloroethane.
  • aromatic compounds such as toluene, xylene, ethylbenzene, and jetylbenzene
  • aliphatic compounds such as octane and decane
  • alicyclic compounds such as decalin
  • esters such as butyl acetate and pentyl acetate
  • Xylene and ethylbenzene are preferable because they have an appropriate boiling point, are less degassed, and have no adverse effect on polymerization.
  • the amount of the solvent varies depending on the boiling point of the solvent.
  • the amount of the solvent is 30% by weight or less, preferably 20% by weight or less, based on the weight of the entire mixture at the time of polymerization. If no solvent is used during polymerization, bulk polymerization occurs.
  • the polymerization initiator used in the solution polymerization method and bulk polymerization method is one that decomposes actively at the polymerization temperature to generate radicals.
  • mercabtans are mainly used as the molecular weight regulator used in this case.
  • the mercaptans include n-butyl mercaptan, isobutyl mercaptan, n-octyl mercaptan, n-dodecyl mercaptan, sec-dodecyl mercaptan, t-butyl mercaptan, felt mercaptan, tiocresol, thioglycolic acid and the like.
  • esters and ethylenethioglycol examples of these molecular weight modifiers used is preferably 0.01 to 0.5% by weight based on the weight of the total reaction mixture.
  • the polymerization reactor uses a device that is stirred uniformly with a stirring blade such as a double helical ribbon or pitched paddle type.
  • the monomer or monomer solution is continuously supplied to the polymerization reactor, and the polymerization conversion rate of the monomer is substantially constant within a range of 0 to 70%.
  • the polymerization reaction is carried out at a temperature of 160 ° C.
  • the polymerization conversion rate is preferably 40% or more, and the load of the devolatilization process due to the volatile components is reduced. On the other hand, if it is 70% or less, for example, the piping pressure loss between the polymerization reactor and the pre-heater is reduced, so that the polymerization liquid can be easily transported.
  • the polymerization temperature is 120 ° C or higher, the polymerization rate is practical.
  • the polymerization temperature is 160 ° C or lower, the polymerization rate is appropriate, and the polymerization conversion rate can be easily adjusted. Further, it is preferable since the heat decomposability is not lowered.
  • the polymerization solution obtained by such a polymerization reaction is devolatilized and the polymer is taken out.
  • the devolatilizer an extruder with a multistage vent, a devolatilization tank, or the like is used.
  • the polymerization solution is superheated to a temperature of 200 to 290 ° C with a pre-heater or the like, has a sufficient space at the top, and 200 to 250 ° C, a temperature of 2.7 to 13 kPa, under vacuum Feed to the devolatilization tank and take out the polymer.
  • This polymer is continuously transferred to an extruder in a molten state, extruded through a die from a die into a strand, cooled with water, and cut with a strand cutter to obtain a cylindrical polymer.
  • the flat methacrylic resin can be extruded from an extruder in the same manner as in the production of the cylindrical methacrylic resin, and then cut with an underwater cutter.
  • a release agent, a colorant, an ultraviolet absorber, an antioxidant, a light diffusing agent, a plasticizer, and the like are added using a feed pump from the side portion of the extruder. That's right.
  • the shape of the columnar polymer which is an important component of the present invention, is defined by the major axis (al), minor axis (b 1), and length (L) of the cross section.
  • the apparent density of the columnar or flat methacrylic rosin polymer is from 0.63 gZml to 0.6.
  • the amorphous metataryl rosin polymer which is an important constituent of the present invention, is formed into a plate shape by melt extrusion or the like from the above-mentioned suspension polymerization, solution polymerization, or bulk polymerization. It is obtained by mechanically grinding the material.
  • an impact pulverizer such as an impact crusher, a hammer crusher or a shear pulverizer such as a cutter mill can be used.
  • the cutter mill is preferable because the size of the pulverized product can be adjusted depending on the size of the screen holes.
  • a screen having a diameter of about 8 to 12 ⁇ is usually used, and an irregularly-shaped methallyl rosin polymer that has passed through this screen is used in the present invention.
  • the regular-shaped methacrylic resin and the irregular-shaped methacrylic resin polymer are mixed and used as a raw material for extruding methallyl resin. It is important that the mixing ratio of the regular-shaped methacrylic resin and the irregular-shaped methacrylic resin polymer is mixed so that the apparent density of the mixture is 0.80 gZml or more. When the apparent density of the mixture is 0.80 gZml or more, the extrusion stability is excellent, and an extruded plate with good thickness accuracy can be obtained.
  • the preferred mixing ratio of each polymer varies depending on the size of the polymer.
  • the amorphous methacrylic resin is 5 to 380 parts by weight, preferably 10 to 330 parts by weight, with respect to 100 parts by weight of the regular methacrylic resin.
  • the amount is preferably 10 to 230 parts by weight.
  • the proportion of the spherical, cylindrical, Z or flat methallyl slag polymer in the regular-shaped methacrylic slag polymer is cylindrical, Z or flat methacrylic slag relative to 100 parts by weight of the spherical methallyl succinic polymer.
  • the fat polymer is 0 to 400 parts by weight, preferably 0 to 250 parts by weight, and more preferably 0 to 150 parts by weight.
  • the extruded plate of the present invention can be produced by a usual melt extrusion method. For example, a mixture of the regular shape methacrylic resin and the irregular shape methacrylic resin polymer of the present invention is melted at 220 to 300 ° C., then extruded into a plate shape through a T-die, the surface is finished with a polishing roll, cooled, and then cut. A plate-like body can be obtained.
  • the plate thickness accuracy is the difference between the average value of the plate thickness measured at intervals of 50 mm and the maximum and minimum values of the measurement points for a plate having a width of 1000 mm.
  • the plate thickness accuracy is within ⁇ 1.0% of the average plate thickness, preferably within ⁇ 0.5%.
  • the plate thickness accuracy is within ⁇ 0.5% of the average plate thickness.
  • the metathalyl resin extruded plate of the present invention has the effect of maximally improving the light emission efficiency of light that has also entered the light source lamp force and reducing luminance spots.
  • An electromagnetic shaking sieving meter (electromagnetic vibration AS200 DISIT manufactured by Mitamura Riken Kogyo Co., Ltd.) was used. Sample lOOg is placed on top of the 7-stage sieve of the size 500-425-355-300-250-150-150, and shaken with a sieve shaker for 10 minutes, then spherical on each sieve. The metataryl rosin polymer was weighed, a cumulative residual distribution curve was written, the median diameter was determined, and the average particle diameter was obtained. For polymers with a small average particle size, measurements were made using a seven-stage sieve with a nominal size of 300-250-180-125-100-63-63.
  • a 1000 mm wide plate shown in Fig. 1 measurements were made up to 0.00 lmm using a 19 point outside micrometer (MDC-25M manufactured by Mitutoyo Corporation) at 50 mm intervals. The average value of each measurement point was determined, and the plate thickness accuracy was calculated from the average value and the maximum value and minimum value of each measurement point.
  • the plate thickness accuracy of the maximum thickness is “plate thickness accuracy A”
  • the plate thickness accuracy of the minimum thickness is “plate thickness accuracy B”.
  • Thickness accuracy—A (%) (Maximum value—Average value) Z Average value X 100 (1)
  • Sheet thickness accuracy B (%) (Minimum value average value) Z Average value X 100 (2)
  • a cold cathode tube of 3mm ⁇ (made by Harrison Electric Co., Ltd.) is installed as a light source on both end faces of the light guide plate at the length of 319mm, and Ray White 75 (made by Kimoto) is used as a light reflecting sheet. And two light diffusion sheets D121 (made by Gidden) were placed on the top of the light guide plate.
  • the cold cathode tube was charged with a voltage of 12V from a DC voltage stabilizer and lit for 20 minutes after being lit for 20 minutes.
  • the luminance meter (CA-1000: manufactured by Minolta) installed at a position distant from the light emitting surface vertically 19 X horizontal
  • the average luminance was calculated from the 361 measured values obtained in the above.
  • the uniformity was calculated from the obtained 361 measured values as an evaluation index of luminance spots by the following formula (3).
  • Luminance uniformity (%) Minimum luminance value Z Maximum luminance value X 100 (3)
  • the polymerization solution was continuously taken out from the polymerization reactor, then heated to 260 ° C with a heating plate, and cast and dropped through the space between the heating plates.
  • a devolatilization tank maintained at 2.7 kPa, 230 ° C, separated the polymer from unreacted monomers and solvent.
  • the polymer is continuously transferred to the extruder in a molten state, extruded through the extruder into a strand from a die, water-cooled (water temperature: 60 ° C bath), cut with a strand cutter, and melt flow rate ( I SO 1139 Condi 3) 1.
  • a 10-minute cylindrical methacrylic resin (polymer B) was obtained.
  • the major axis (al), minor axis (bl), and length (L) of polymer—B are (al) 2. 773mm, (bl) 2. 689mm, (L) 3. 105mm, (bl) / ( al) It was 0.97 and the apparent density was 0.67 gZml.
  • polymer B In the production process of polymer B, instead of extruding into a strand from a die and then cooling with water and then cutting with a cutter, it is cut with an underwater cut method that extrudes and cuts into water from a die, and melt flowlay HISO-1139—Condl3) l.
  • Polymer — D major axis (a2), minor axis (b2), thickness (T) are (a2) 3. 178mm, (b2) 3. 089mm, (T) l. 505mm, (b2) / (a2) 0.97, apparent density 0.668 g / ml.
  • Polymer — 150mm ⁇ single screw extrusion with A and T die for sheet die temperature: 250 ° C
  • Machine cylinder temperature: 200 ° C -210 ° C -210 ° C -260 ° C -260 ° C -240 ° C) from the feed side
  • three poly cinder rolls roll temperature: 80 ° C)
  • an extrusion sheet forming machine comprising a take-up device, and extruded with a extrusion amount of 600 kgZhr to obtain a methacrylic resin extruded plate having a width of 1000 mm and a thickness of 6 mm.
  • this extruded plate was pulverized by using a pulverizer (U10-30120XLFX type) (screen: 10 mm ⁇ ) manufactured by Horai Co., Ltd. to obtain an irregular-shaped metataryl rosin polymer (polymer D).
  • the apparent density of Polymer-D was 0.60 gZml.
  • the resulting extruded plate was cut into a size of 241 mm in width and 319 mm in length using a circular saw, and the cut surface of the cut plate was cut using a precision polishing machine (PLA—Beauty: manufactured by Megalotech-Power Co., Ltd.). Polish and then puffed to give a mirror finish.
  • PPA Precision Polishing machine
  • screen printing was performed on one side of the light guide plate to obtain a light guide plate. Table 1 shows the measurement results of luminance and luminance spots.
  • Extruded plate B was obtained in the same manner as in Example 1 except that the amount was 88 g / ml). As in Example 1, thickness measurement, brightness, and brightness spots were measured, and the results are shown in Table 1.
  • Extruded plate C was obtained in the same manner as in Example 1 except that the mixture (polymer apparently used in Example 1) had a blending amount of 400 parts by weight (apparent density 0.75 g / ml). As in Example 1, thickness measurement, brightness, and brightness spots were measured, and the results are shown in Table 1. ⁇ Comparative Examples 2, 3>
  • Polymer A (apparent density 0.76 gZml) and polymer D (apparent density 0.60 gZml) used in Example 1 were each extruded in the same manner as in Example 1 and extruded plate D and extruded plate E Obtained.
  • thickness measurement, luminance, and luminance spots were measured, and the results are shown in Table 1.
  • Example 1 The polymer used in Example 1 was replaced with Example 1 except that the polymer (A50 parts by weight) and the polymer (B50 parts by weight) were used instead of A100 parts by weight. In the same manner, Extruded Plate-F was obtained. As in Example 1, thickness measurement, luminance, and luminance spots were measured, and the results are shown in Table 1.
  • Extruded plate-G was obtained in the same manner as in Example 1, except that the mixture was changed to a mixture using the polymer C instead of the polymer B used in Example 3 (apparent density 0.87 gZml). As in Example 1, thickness measurement, luminance, and luminance spots were measured, and the results are shown in Table 1.
  • Example 1 Using the extruded raw material of Example 1, a methacrylic resin extruded plate (extruded plate H) having a thickness of 8 mm was formed, and in the same manner as in Example 1, thickness measurement, luminance, and luminance unevenness were measured. The results are shown in Table 1
  • the light guide plate of the present invention is used in office automation equipment such as personal computers and word processors, various monitors for displaying image signals, for example, display devices used for panel monitors, television monitors and the like, and lighting devices for indoor and outdoor spaces. It can be suitably used for display devices and signboards.
  • FIG. 1 Shows thickness measurement points in the present invention.
  • FIG. 2 shows an example of a luminance evaluation method in an edge light type liquid crystal light source device using the light guide plate of the present invention.

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Abstract

There is provided a methacrylic resin extrusion plate formed by a mixture having an apparent density of 0.80 g/ml or above prepared by mixing methacrylic resin polymer of a definite shape having an apparent density of 0.63 g/ml to 0.78 g/ml and methacrylic resin polymer of an indefinite shape having an apparent density of 0.55 g/ml to 0.63 g/ml. The plate thickness accuracy in the width direction is controlled to be within ± 1.0% of the average plate thickness. The methacrylic resin extrusion plate for a light guide plate is preferably used for office automation devices such as a personal computer and a word processor, display devices used for various monitors displaying an image signal such as a panel monitor and a television monitor, display devices used for indoor or outdoor illumination devices and sign boards.

Description

明 細 書  Specification
光学用メタクリル樹脂押出板の製造方法  Method for producing methacrylic resin extrusion plate for optics
技術分野  Technical field
[0001] 本発明は、パーソナルコンピュータやワードプロセッサなどのオフィスオートメーショ ン機器、画像信号を表示する各種モニター、例えばパネルモニター、テレビモニター 等に用いられる表示装置及び室内外空間の面光源装置に使用される表示装置や看 板等に適した導光板用メタクリル榭脂押出板の製造方法に関する。  The present invention is used for office automation equipment such as personal computers and word processors, various monitors for displaying image signals, for example, display devices used for panel monitors, television monitors and the like, and surface light source devices for indoor and outdoor spaces. The present invention relates to a method for producing a methacrylic resin extruded plate for a light guide plate suitable for a display device or a signboard.
背景技術  Background art
[0002] 透明熱可塑性榭脂、その中でも特にメタタリル榭脂は、優れた光透過性、機械的特 性力もこれまでに多くの照明用途に用いられてきたが、特に近年は照明用ランプを 備えた表示装置等のバックライト用導光板として使用されるようになってきた。このバ ックライトの方式としては、導光板を光源と液晶ユニットの間に挟んだ、いわゆる直下 式と、光源を導光板のエッジに取り付けるエッジライト方式の 2種が通常用いられ、現 在はエッジライト方式が主流となっている。近年は表示装置の高輝度化、大型化、薄 型化の要求が強ぐより明るく、より大きぐより薄くの商品コンセプトのもと開発が続け られている。特にエッジライト方式での高輝度面発光装置の開発が強く望まれている  [0002] Transparent thermoplastic resin, and in particular, methallyl resin, in particular, has been used for many lighting applications because of its excellent light transmission and mechanical properties. It has come to be used as a light guide plate for backlights of display devices. There are two commonly used backlight systems: the so-called direct type, in which the light guide plate is sandwiched between the light source and the liquid crystal unit, and the edge light method in which the light source is attached to the edge of the light guide plate. The method has become mainstream. In recent years, development has continued under the concept of brighter, larger and thinner products, where the demand for higher brightness, larger size, and thinner display devices is stronger. In particular, there is a strong demand for the development of high-intensity surface emitting devices using the edge light method.
[0003] この為、光源装置で使用される導光板についても、側面に配設された光源ランプよ り入光した光の入射光を効率的に出射面に出射させる導光板の要求が非常に強く なっている。 [0003] For this reason, the light guide plate used in the light source device also has a great demand for a light guide plate that efficiently emits incident light of light incident from the light source lamp disposed on the side surface to the output surface. It is getting stronger.
[0004] しかし、通常の押出板では、押出し方向の板厚変動は少ないが、幅方向の板厚変 動が大きぐ光源装置に配設された光源ランプより入光した光が不規則に出光され輝 度均斉性に劣り、高輝度が得られない。  [0004] However, in a normal extruded plate, although the thickness variation in the extrusion direction is small, the light incident from the light source lamp disposed in the light source device in which the thickness variation in the width direction is large is irregularly emitted. However, the brightness uniformity is inferior and high brightness cannot be obtained.
導光板による高輝度化の方法に関しては、これまでにも複数の技術開示がなされ ている。例えば、導光板の中に光拡散粒子を分散混入することにより均一な発光面 を得る方法 (例えば、特許文献 1参照)、導光体に屈折率の異なる微粒子を包含する 光散乱性プラスチック材料を用いることにより高輝度化する方法等が開示されている (例えば、特許文献 2参照)が工程が煩雑である。 A number of technical disclosures have been made so far regarding the method of increasing the brightness using the light guide plate. For example, a method of obtaining a uniform light emitting surface by dispersing and diffusing light diffusing particles in a light guide plate (see, for example, Patent Document 1), and a light scattering plastic material including fine particles having different refractive indexes in a light guide. A method of increasing the brightness by using it is disclosed. (For example, see Patent Document 2), the process is complicated.
[0005] 特許文献 1 :特公昭 39— 1194号公報 [0005] Patent Document 1: Japanese Patent Publication No. 39-1194
特許文献 2 :特開平 4— 145485号公報  Patent Document 2: JP-A-4-145485
発明の開示  Disclosure of the invention
発明が解決しょうとする課題  Problems to be solved by the invention
[0006] し力しながら、これら煩雑な微粒子を含有するメタクリル榭脂を用いる技術以外、輝 度及び輝度斑等、表示装置の大型化、薄型化に伴う要求に対し充分対応できるレべ ルには到達して 、な 、のが現状である。 [0006] However, in addition to the technology using methacrylic resin containing these complicated fine particles, the level can sufficiently meet the demands associated with the increase in size and thickness of display devices, such as brightness and luminance spots. It is the current situation that has been reached.
[0007] 本発明の目的は、画像信号を表示する各種モニター、例えばパネルモニター、テ レビモニター等に用いられる表示装置及び室内外空間の照明装置に使用される表 示装置や看板等に適した導光板用メタクリル榭脂押出板及びその製造方法を提供 することにある。 [0007] An object of the present invention is suitable for various monitors that display image signals, for example, display devices used for panel monitors, television monitors and the like, and display devices and signboards used for indoor and outdoor lighting devices. An object is to provide a methacrylic resin extruded plate for a light guide plate and a method for producing the same.
課題を解決するための手段  Means for solving the problem
[0008] 本発明者等は、前記課題を解決するため鋭意検討の結果、定形状を有するメタタリ ル榭脂押出原料に不定形状を有するメタタリル榭脂押出原料を特定の割合で混合し 、押出成型されたメタクリル榭脂板を導光板として用いる事により高輝度化、輝度斑 低減する事を見出し、本発明を完成させるに至った。 [0008] As a result of intensive studies to solve the above-mentioned problems, the present inventors mixed a metataryl resin extruded material having an irregular shape with a metataryl resin extruded material having a fixed shape at a specific ratio, and then extrusion molding. By using the methacrylic resin plate used as a light guide plate, it was found that the brightness was increased and the brightness unevenness was reduced, and the present invention was completed.
すなわち、本発明は  That is, the present invention
[1] 見掛け密度 0. 63gZml〜0. 78gZmlの定形状メタクリル榭脂重合体と見 掛け密度 0. 55gZml〜0. 63gZmlの不定形状メタクリル樹脂重合体とを見掛け密 度が 0. 80gZml以上となるように混合し、得られた混合物を押出し成形して、板厚 が 2. 0-15. Ommであって、幅方向の板厚精度が平均板厚の ± 1. 0%以内である 導光板用メタクリル榭脂押出板を製造する方法、  [1] The apparent density between the apparent density methacrylic resin having an apparent density of 0.63 gZml to 0.78 gZml and the amorphous methacrylic resin polymer having an apparent density of 0.55 gZml to 0.63 gZml is at least 0.80 gZml. The resulting mixture is extruded, and the thickness is 2.0-15. Omm, and the thickness accuracy in the width direction is within ± 1.0% of the average thickness. Method for producing a methacrylic resin extruded plate for
[2] 該板厚が 3. 5〜8. 5mmであり、且つ幅方向の板厚精度が平均板厚の ±0. 5%以内であることを特徴とする、請求項 1記載の導光板用メタクリル榭脂押出板の 製造方法、  [2] The light guide plate according to claim 1, wherein the plate thickness is 3.5 to 8.5 mm, and the plate thickness accuracy in the width direction is within ± 0.5% of the average plate thickness. For producing methacrylic resin extruded plate for
[3] 上記 1または 2記載の方法で製造した導光板用メタクリル榭脂押出板、 である。 [0009] 本発明について、以下具体的に説明する。 [3] A methacrylic resin extruded plate for a light guide plate produced by the method described in 1 or 2 above. [0009] The present invention will be specifically described below.
[0010] 本発明にお 、て用いられるメタクリル樹脂とはメタクリル酸メチルある!/ヽはメタクリル 酸ェチルを 70重量%以上と、これらと共重合性を有する単量体とを共重合することに より得る事ができる。これらと共重合性を有する単量体としてはメタクリル酸プチル、メ タクリル酸ェチル、メタクリル酸メチル、メタクリル酸プロピル、メタクリル酸シクロへキシ ル、メタクリル酸フエ-ル、メタクリル酸 2—ェチルへキシルなどのメタクリル酸エステル 類、アクリル酸メチル、アクリル酸ェチル、アクリル酸ブチル、アクリル酸シクロへキシ ル、アクリル酸フエ-ル、アクリル酸 2—ェチルへキシル等のアクリル酸エステル類、メ タクリル酸、アクリル酸等の不飽和酸類等があげられる力 これらに限定されるもので はない。  [0010] The methacrylic resin used in the present invention is methyl methacrylate! The / soot can be obtained by copolymerizing 70% by weight or more of methacrylic acid methacrylate and a monomer having copolymerizability with these. Monomers that are copolymerizable with these include butyl methacrylate, ethyl methacrylate, methyl methacrylate, propyl methacrylate, cyclohexyl methacrylate, methacrylate methacrylate, 2-ethylhexyl methacrylate, etc. Methacrylic acid esters, Methyl acrylate, Ethyl acrylate, Butyl acrylate, Acrylic acid cyclohexyl, Acrylic acid ester, Acrylic acid ester such as 2-Ethylhexyl acrylate, Methacrylic acid, Acrylic The power of unsaturated acids such as acids is not limited to these.
本発明で用いられる定形状メタクリル榭脂押出原料とは、重合反応により得られる 球状もしくは円柱状または扁平状のメタクリル榭脂を 、う。不定形状メタタリル榭脂押 出原料とは、一度板状に成型されたメタクリル榭脂成型体を機械的に粉砕処理され て得られるメタクルリル榭脂を ヽぅ。  The regular-shaped methacrylic resin extruded raw material used in the present invention is a spherical, cylindrical or flat methacrylic resin obtained by a polymerization reaction. The unshaped metataryl resin extrusion raw material is methacrylic resin obtained by mechanically crushing a methacrylic resin molding once formed into a plate shape.
[0011] 球状メタクリル樹脂は、懸濁重合法により得られる。懸濁重合法について説明する。 [0011] The spherical methacrylic resin is obtained by a suspension polymerization method. The suspension polymerization method will be described.
まずメタクリル酸メチルあるいはメタクリル酸ェチルと他の単量体と力 なる単量体混 合物に、重合開始剤および連鎖移動剤を均一に溶解させる。該均一溶解物を分散 安定剤が存在する水媒体に懸濁した後、所定の重合温度で一定時間保持して重合 を完結させ、その得られた混濁重合物を濾過し、水洗、乾燥する事により得られる。 懸濁重合の際に使用される重合開始剤としては、ビニル単量体の重合用として周 知のラジカル重合開始剤でよい。例えば、ァゾビスイソブチ口-トリル、 2, 2' ァゾビ ス(2, 4 ジメチルバレ口-トリル)、ジメチルー 2, 2,ーァゾビスイソブチレート、 tーブ チルパーォキシピバレート、 t ブチルパーォキシ 2—ェチルへキサエート、クミルパ 一ォキシ 2—ェチルへキサノエート、ベンゾィルパーオキサイド、ラウロイルパーォキ サイド等を挙げることが出来る。これらのラジカル重合開始剤の使用量は、単量体ま たは単量体混合物 100重量部に対して通常 0. 01〜2. 0重量部の範囲が好ましい。 懸濁重合の際に使用される連鎖移動剤としては、メタクリル酸メチルの重合に用い られる周知のものでよい。例えば、 tーブチルメルカプタン、 n—ブチルメルカプタン、 n—ォクチルメルカプタン、 n—ドデシルメルカプタン等を挙げることが出来る。これら の連鎖移動剤の使用量は、単量体又は単量体混合物 100重量部に対して通常 0. 0 1〜2. 0重量部の範囲が好ましい。 First, a polymerization initiator and a chain transfer agent are uniformly dissolved in a monomer mixture consisting of methyl methacrylate or ethyl methacrylate and another monomer. The homogeneously dissolved product is suspended in an aqueous medium containing a dispersion stabilizer and then held at a predetermined polymerization temperature for a certain period of time to complete the polymerization. The resulting turbid polymer is filtered, washed with water and dried. Is obtained. The polymerization initiator used in suspension polymerization may be a radical polymerization initiator known for polymerization of vinyl monomers. For example, azobisisobutyrate-tolyl, 2,2 'azobis (2,4 dimethylvale-tolyl), dimethyl-2,2, -azobisisobutyrate, tert-butylperoxypivalate, tert-butylperoxy 2- Examples include ethyl hexaate, cumyl paroxy 2-ethyl hexanoate, benzoyl peroxide, lauroyl peroxide, and the like. These radical polymerization initiators are preferably used in an amount of usually 0.01 to 2.0 parts by weight per 100 parts by weight of the monomer or monomer mixture. The chain transfer agent used in the suspension polymerization may be a well-known one used for polymerization of methyl methacrylate. For example, t-butyl mercaptan, n-butyl mercaptan, Examples thereof include n-octyl mercaptan and n-dodecyl mercaptan. The amount of these chain transfer agents used is usually preferably in the range of 0.01 to 2.0 parts by weight per 100 parts by weight of the monomer or monomer mixture.
懸濁重合の際に使用される分散安定剤としては、特に限定されないが、リン酸カル シゥム、炭酸カルシウム、水酸ィ匕アルミニウム等の水難溶性無機化合物、ポリビュル アルコール、ポリエチレンオキサイド、セルロース誘導体のノ-オン系高分子化合物、 ポリアクリル酸及びその塩、ポリメタクリル酸及びその塩、メタクリル酸エステルとメタク リル酸及びその塩との共重合物等のァ-オン系高分子化合物を挙げることが出来る 。これらの分散安定剤の使用量は、水 100重量部に対し 0. 01〜5. 0重量部の範囲 が好ましい。  The dispersion stabilizer used in the suspension polymerization is not particularly limited. However, it is a poorly water-soluble inorganic compound such as calcium phosphate, calcium carbonate, and aluminum hydroxide, polybutal alcohol, polyethylene oxide, and cellulose derivative. -On-based polymer compounds, polyacrylic acid and its salts, polymethacrylic acid and its salts, copolymer of methacrylic acid ester and methacrylic acid and its salts, etc. . The amount of these dispersion stabilizers used is preferably in the range of 0.01 to 5.0 parts by weight per 100 parts by weight of water.
懸濁重合の際に使用される水としては、純水、イオン交換水、脱イオン水等が挙げ られる。水の使用量は、特に限定されないが、単量体又は単量体混合物 100重量部 に対して 100〜250重量部の範囲が好まし!/、。  Examples of water used in the suspension polymerization include pure water, ion exchange water, and deionized water. The amount of water used is not particularly limited, but is preferably in the range of 100 to 250 parts by weight per 100 parts by weight of the monomer or monomer mixture! /.
また、懸濁重合の重合温度としては、特に限定されないが、 60〜120°C程度で、用 いる重合開始剤に適した温度とする。重合装置としては、周知の攪拌翼例えばター ビン翼、ファウドラー翼、プロペラ翼、ブルーマージン翼等の翼のついた攪拌機を備 えた重合容器を用い、該容器には、ノ ッフルをつけているのが一般的である。  The polymerization temperature for suspension polymerization is not particularly limited, but is about 60 to 120 ° C and is suitable for the polymerization initiator used. As a polymerization apparatus, a polymerization vessel equipped with a well-known stirring blade, for example, a turbine blade, a fiddler blade, a propeller blade, a blue margin blade, or the like, is used, and the vessel is provided with a kaffle. Is common.
さらに必要に応じて離型剤、着色剤、紫外線吸収剤、酸化防止剤、光拡散剤、可 塑剤等を懸濁させ重合させても良 ヽ。  Furthermore, if necessary, a release agent, a colorant, an ultraviolet absorber, an antioxidant, a light diffusing agent, a plasticizer, etc. may be suspended and polymerized.
懸濁重合の終了後は、周知の方法により洗浄、脱水、乾燥すること〖こより球状メタク リル榭脂重合体を得ることができる。  After the completion of the suspension polymerization, the spherical methacrylate resin can be obtained by washing, dehydrating and drying by a known method.
本発明の重要構成要件である球状メタタリル榭脂重合体の平均粒子径は 0. 2〜0 . 5mmであり、好ましくは 0. 25-0. 39mmである。 0. 2mm以上で良好な板厚精度 が得ることができ、また 0. 5mm以下で平均粒子径を有する重合体を安定して製造 することができる。また、見掛け密度が 0. 70g/ml〜0. 78g/mlの範囲内であると 良好な板厚精度を得ることができる。  The average particle size of the spherical methallyl succinic polymer, which is an important constituent of the present invention, is 0.2 to 0.5 mm, preferably 0.25 to 0.39 mm. Good plate thickness accuracy can be obtained when the thickness is 0.2 mm or more, and a polymer having an average particle diameter of 0.5 mm or less can be stably produced. Further, when the apparent density is in the range of 0.70 g / ml to 0.78 g / ml, good thickness accuracy can be obtained.
次ぎに本発明の重要な構成要件である円柱状または扁平状メタクリル榭脂重合体 につ 、て説明する。円柱状メタクリル榭脂重合体は上記懸濁重合で得られた球状メ タクリル榭脂重合体をベント付押出機に供給し、温度 220〜260°C、ベント真空圧力 1. 3〜8kPaで押出しダイスよりストランド状に押出し、水冷し、ストランドカッターで切 断し得られる。他には公知の溶液重合法、塊状重合法により得られる溶融状態のメタ クリル樹脂重合体を押出しダイスよりストランド状に押出し、水冷し、ストランドカッター で切断し得られる。扁平状メタクリル榭脂重合体は上記円柱状メタクリル榭脂重合体 製造と同様にしてベント付押出機より押出され、ついでアンダーウォーターカッターで カッティングされ得られる。 Next, a columnar or flat methacrylic resin, which is an important constituent element of the present invention, will be described. Cylindrical methacrylic resin is a spherical polymer obtained by suspension polymerization. Tacryl resin can be supplied to an extruder equipped with a vent, extruded at a temperature of 220 to 260 ° C and vented vacuum pressure of 1.3 to 8 kPa in a strand from an extrusion die, water cooled, and cut with a strand cutter. Alternatively, a molten methacrylic resin polymer obtained by a known solution polymerization method or bulk polymerization method can be extruded into a strand shape from an extrusion die, cooled with water, and cut with a strand cutter. The flat methacrylic resin can be extruded from an extruder with a vent in the same manner as in the production of the cylindrical methacrylic resin, and then cut with an underwater cutter.
溶液重合法、塊状重合法の例としては以下の方法が挙げられる。溶液重合法にお ける溶媒は、蒸留塔ボトム及び蒸留塔内部でメタクリル酸メチル単量体及びメタクリル 酸メチル単量体及びメタクリル酸メチルと共重合可能な単量体より高い沸点を有して いるのが好ましい。、具体的には、トルエン、キシレン、ェチルベンゼン、ジェチルべ ンゼン等の芳香族化合物、オクタン、デカン等の脂肪族化合物、デカリン等の脂環族 化合物、酢酸ブチル、酢酸ペンチル等のエステル類、 1, 1, 2, 2—テトラクロロェタン 等のハロゲン化合物が挙げられる。特にアルキルベンゼン、さらにその中でトルエン Examples of the solution polymerization method and the bulk polymerization method include the following methods. The solvent in the solution polymerization method has a higher boiling point than the methyl methacrylate monomer, the methyl methacrylate monomer, and the monomer copolymerizable with methyl methacrylate at the bottom and inside of the distillation column. Is preferred. Specifically, aromatic compounds such as toluene, xylene, ethylbenzene, and jetylbenzene, aliphatic compounds such as octane and decane, alicyclic compounds such as decalin, esters such as butyl acetate and pentyl acetate, 1, And halogen compounds such as 1, 2, 2-tetrachloroethane. Especially alkylbenzene, and moreover toluene
、キシレン、ェチルベンゼンが適度な沸点を有し、脱気にも負荷が少なぐ又重合に 悪影響を及ぼすこともなく好ましい。溶媒量は溶媒の沸点によっても異なる力 重合 時の全混合物の重量に基づき 30重量%以下、好ましくは 20重量%以下である。重 合時に溶媒を使用しなければ、塊状重合となる。 Xylene and ethylbenzene are preferable because they have an appropriate boiling point, are less degassed, and have no adverse effect on polymerization. The amount of the solvent varies depending on the boiling point of the solvent. The amount of the solvent is 30% by weight or less, preferably 20% by weight or less, based on the weight of the entire mixture at the time of polymerization. If no solvent is used during polymerization, bulk polymerization occurs.
溶液重合法、塊状重合法で使用される重合開始剤は、重合温度で活性に分解しラ ジカルを発生するもので、例えば、ジー t ブチルパーォキシド、ジクミルパーォキシ ド、メチルェチルケトンパーォキシド、ジー t ブチルパーフタレート、ジー t ブチル パーべンゾエート、 t ブチルパーアセテート、 2, 5 ジメチルー 2, 5 ジ(tーブチ ルバーオキシ)へキサン、 1, 1—ビス(t—ブチルパーォキシ)—3, 3, 5 トリメチル シクロへキサン、 1, 1—ビス(t—ブチルパーォキシ)シクロへキサン、ジ— t—ァミル パーォキシド、ベンゾィルパーォキシド、クメンハイド口パーォキシド、ラウリルバーオ キシド、ァゾビスイソブタノールジアセテート、 1, 1 'ーァゾビスシクロへキサンカルボ 二トリル、 2 フエ二ルァゾ 2, 4 ジメチル一 4—メトキシバレロ-トリル、 2 シァノ 2 , 2—プロピルァゾホルムァシド、 2, 2,ーァゾビスイソブチ口-トリル等を挙げることが 出来る。これら重合開始剤の使用量は、全反応混合物の重量に基づき 0. 001-0. 03重量%が好ましい。 The polymerization initiator used in the solution polymerization method and bulk polymerization method is one that decomposes actively at the polymerization temperature to generate radicals. Ketone peroxide, di-t-butyl perphthalate, di-t-butyl perbenzoate, t-butyl peracetate, 2,5-dimethyl-2,5-di (tert-butylberoxy) hexane, 1,1-bis (t-butylperoxy) — 3, 3, 5 Trimethylcyclohexane, 1,1-bis (t-butylperoxy) cyclohexane, di-t-amyl peroxide, benzoyl peroxide, cumene hydride peroxide, lauryl baroxide, azobisisobutanol di Acetate, 1, 1'-azobiscyclohexanecarbo nitrile, 2 phenyl 2, 4, dimethyl mono 4-methoxyvalero- Lil, 2 Shiano 2, 2-propyl § zone Holm § Sid, 2, 2, over § zone bis isobutyronitrile port - be mentioned tolyl I can do it. The amount of these polymerization initiators used is preferably 0.001 to 0.03% by weight based on the weight of the total reaction mixture.
更に、この際に使用する分子量調節剤は、主としてメルカブタン類が使用される。メ ルカブタン類としては、例えば、 n—ブチルメルカプタン、イソブチルメルカプタン、 n ーォクチルメルカプタン、 n—ドデシルメルカプタン、 sec—ドデシルメルカプタン、 t— ブチルメルカプタン、フエ-ルメルカプタン、チォクレゾール、チォグリコール酸とその エステル及びエチレンチォグリコール等が挙げることが出来る。これら分子量調整剤 の使用量は、全反応混合物の重量に基づき 0. 01〜0. 5重量%が好ましい。  In addition, mercabtans are mainly used as the molecular weight regulator used in this case. Examples of the mercaptans include n-butyl mercaptan, isobutyl mercaptan, n-octyl mercaptan, n-dodecyl mercaptan, sec-dodecyl mercaptan, t-butyl mercaptan, felt mercaptan, tiocresol, thioglycolic acid and the like. Examples thereof include esters and ethylenethioglycol. The amount of these molecular weight modifiers used is preferably 0.01 to 0.5% by weight based on the weight of the total reaction mixture.
重合反応機はダブルへリカルリボン、ピッチドバドル型などの攪拌翼で均一に攪拌 されて ヽる装置を使用する。重合は単量体又は単量体溶液を重合反応機に連続し て供給し、単量体の重合転ィ匕率力 0〜70%の範囲内で実質的に一定になる様に 1 20〜160°Cの温度で重合反応を実施する。重合転化率が 40%以上で、揮発成分 による脱揮工程の負荷が小さくなり、例えば予備加熱器の伝熱面積の制約力ゝら脱揮 不十分になることもなくなり好ましい。一方、 70%以下では、例えば、重合反応機から 予備加熱器間での配管圧力損失が少なくなつて、重合液の輸送が容易となり好まし い。重合温度が 120°C以上では重合速度が実用的で、また 160°C以下では重合速 度が適当で、重合転化率の調整が容易である。また、耐熱分解性が低下することも なく好ましい。  The polymerization reactor uses a device that is stirred uniformly with a stirring blade such as a double helical ribbon or pitched paddle type. In the polymerization, the monomer or monomer solution is continuously supplied to the polymerization reactor, and the polymerization conversion rate of the monomer is substantially constant within a range of 0 to 70%. The polymerization reaction is carried out at a temperature of 160 ° C. The polymerization conversion rate is preferably 40% or more, and the load of the devolatilization process due to the volatile components is reduced. On the other hand, if it is 70% or less, for example, the piping pressure loss between the polymerization reactor and the pre-heater is reduced, so that the polymerization liquid can be easily transported. When the polymerization temperature is 120 ° C or higher, the polymerization rate is practical. When the polymerization temperature is 160 ° C or lower, the polymerization rate is appropriate, and the polymerization conversion rate can be easily adjusted. Further, it is preferable since the heat decomposability is not lowered.
この様な重合反応により得られた重合液は、脱揮して重合物を取出す。脱揮装置 としては、多段ベント付き押出機、脱揮タンクなどを使用する。好ましくは、重合液を 予備加熱器などで 200〜290°Cの温度に過熱し、上部に十分な空間を有し、且つ 2 00〜250°C、 2. 7〜13kPaの温度、真空下の脱揮タンクにフィードして重合物を取 り出す。  The polymerization solution obtained by such a polymerization reaction is devolatilized and the polymer is taken out. As the devolatilizer, an extruder with a multistage vent, a devolatilization tank, or the like is used. Preferably, the polymerization solution is superheated to a temperature of 200 to 290 ° C with a pre-heater or the like, has a sufficient space at the top, and 200 to 250 ° C, a temperature of 2.7 to 13 kPa, under vacuum Feed to the devolatilization tank and take out the polymer.
この重合物は押出機に連続的に溶融状態で移送され、押出機を通してダイスよりスト ランド状に押出され、水冷し、ストランドカッターで切断され、円柱状重合体が得られ る。扁平状メタクリル榭脂重合体は上記円柱状メタクリル榭脂重合体製造と同様にし て押出機より押出され、ついでアンダーウォーターカッターでカッティングされ得られ る。 [0013] さらに必要に応じて、カッティング前に、押出機のサイド部よりフィードポンプを用い て、離型剤、着色剤、紫外線吸収剤、酸化防止剤、光拡散剤、可塑剤等を添加して ちょい。 This polymer is continuously transferred to an extruder in a molten state, extruded through a die from a die into a strand, cooled with water, and cut with a strand cutter to obtain a cylindrical polymer. The flat methacrylic resin can be extruded from an extruder in the same manner as in the production of the cylindrical methacrylic resin, and then cut with an underwater cutter. Furthermore, if necessary, before cutting, a release agent, a colorant, an ultraviolet absorber, an antioxidant, a light diffusing agent, a plasticizer, and the like are added using a feed pump from the side portion of the extruder. That's right.
[0014] 本発明の重要構成要件である円柱状ポリマーの形状は、断面の長径 (al)、短径 (b 1)及び長さ(L)で規定される。長径(al)、短径 (bl)は共に 2. 000-4. OOOmmで あり、(bl)Z(al) =0. 66〜: L 00であり、長さ(L)は 2. 000〜5. OOOmmである。 該範囲内にすることにより良好な板厚精度を得ることができ好ましい。  [0014] The shape of the columnar polymer, which is an important component of the present invention, is defined by the major axis (al), minor axis (b 1), and length (L) of the cross section. The major axis (al) and minor axis (bl) are both 2.000-4. OOOmm, (bl) Z (al) = 0.66 ~: L 00, and the length (L) is 2.000 ~ 5. OOOmm. It is preferable that the thickness is within this range because good thickness accuracy can be obtained.
[0015] 本発明の重要構成要件である扁平状ポリマーの形状は長径 (a2)、短径 (b2)及び 厚さ(T)で規定される。長径(a2)、短径 (b2)は共に 2. 000-4. OOOmmであり、(b2 ) / (a2) =0. 66〜: L . 00であり、厚さ(T)は 1. 000〜3. OOOmmである。該範囲内 にすることにより良好な板厚精度を得ることができ好ましい。  [0015] The shape of the flat polymer, which is an important component of the present invention, is defined by the major axis (a2), minor axis (b2), and thickness (T). Both the major axis (a2) and minor axis (b2) are 2. 000-4. OOOmm, (b2) / (a2) = 0.66 ~: L.00, and the thickness (T) is 1.000. ~ 3. OOOmm. By making it within this range, it is preferable because good thickness accuracy can be obtained.
[0016] また、円柱状または扁平状メタクリル榭脂重合体の見掛け密度が 0. 63gZml〜0.  [0016] Further, the apparent density of the columnar or flat methacrylic rosin polymer is from 0.63 gZml to 0.6.
70gZmlの範囲内であると良好な板厚精度を得ることができる。  When it is within the range of 70 gZml, good thickness accuracy can be obtained.
[0017] 本発明の重要構成要件である不定形状メタタリル榭脂重合体は、前記懸濁重合、 溶液重合、塊状重合から得られたメタタリル榭脂重合体を溶融押出法等により、板状 に成型した材料を機械的に粉砕して得られる。粉砕機としては衝撃式粉砕機、例え ばインパクトクラッシャ、ハンマクラッシャやせん断式粉砕機、例えばカッターミル等が 利用できる。特にカッターミルはスクリーンの孔の大きさによって粉砕品の整粒ができ 好ましい。スクリーン径は通常 8〜12πιπι φ前後のものが用いられ、このスクリーンを 通過した不定形状メタタリル榭脂重合体が本発明に供される。  [0017] The amorphous metataryl rosin polymer, which is an important constituent of the present invention, is formed into a plate shape by melt extrusion or the like from the above-mentioned suspension polymerization, solution polymerization, or bulk polymerization. It is obtained by mechanically grinding the material. As the pulverizer, an impact pulverizer such as an impact crusher, a hammer crusher or a shear pulverizer such as a cutter mill can be used. In particular, the cutter mill is preferable because the size of the pulverized product can be adjusted depending on the size of the screen holes. A screen having a diameter of about 8 to 12πιπιφ is usually used, and an irregularly-shaped methallyl rosin polymer that has passed through this screen is used in the present invention.
[0018] 該不定形状メタタリル榭脂重合体の見掛け密度が 0. 55gZml〜0. 63gZmlの範 囲内であると良好な板厚精度を得ることができる。  [0018] When the apparent density of the irregular-shaped methallyl rosin polymer is in the range of 0.55 gZml to 0.63 gZml, good plate thickness accuracy can be obtained.
[0019] 本発明では、該定形状メタクリル榭脂重合体と該不定形状メタクリル樹脂重合体を 混合してメタタリル榭脂押出用原料として用いる。該定形状メタクリル榭脂重合体と該 不定形状メタクリル樹脂重合体混合割合は混合物の見掛け密度が 0. 80gZml以上 となるように混合されることが重要である。混合物の見掛け密度が 0. 80gZml以上 であると押出し安定性に優れ、良好な板厚精度の押出板を得ることができる。  In the present invention, the regular-shaped methacrylic resin and the irregular-shaped methacrylic resin polymer are mixed and used as a raw material for extruding methallyl resin. It is important that the mixing ratio of the regular-shaped methacrylic resin and the irregular-shaped methacrylic resin polymer is mixed so that the apparent density of the mixture is 0.80 gZml or more. When the apparent density of the mixture is 0.80 gZml or more, the extrusion stability is excellent, and an extruded plate with good thickness accuracy can be obtained.
[0020] 各重合体の好ましい混合割合は重合体の大きさによっても違ってくる力 本願実施 例の重合体粒子径の場合、定形状メタクリル榭脂重合体 100重量部に対して、不定 形メタクリル榭脂重合体は 5〜380重量部であり、好ましくは 10〜330重量部であり、 更に好ましくは 10〜230重量部である。また、定形状メタクリル榭脂重合体中の球状 、円柱状及び Zまたは扁平状のメタタリル榭脂重合体の割合は球状メタタリル榭脂重 合体 100重量部に対して円柱状及び Zまたは扁平状メタクリル榭脂重合体 0〜400 重量部であり、 0〜250重量部が好ましぐ 0〜150重量部が更に好ましい。 [0020] The preferred mixing ratio of each polymer varies depending on the size of the polymer. In the case of the polymer particle size of the example, the amorphous methacrylic resin is 5 to 380 parts by weight, preferably 10 to 330 parts by weight, with respect to 100 parts by weight of the regular methacrylic resin. The amount is preferably 10 to 230 parts by weight. In addition, the proportion of the spherical, cylindrical, Z or flat methallyl slag polymer in the regular-shaped methacrylic slag polymer is cylindrical, Z or flat methacrylic slag relative to 100 parts by weight of the spherical methallyl succinic polymer. The fat polymer is 0 to 400 parts by weight, preferably 0 to 250 parts by weight, and more preferably 0 to 150 parts by weight.
[0021] 本発明の押出板は通常の溶融押出法により作ることが出来る。例えば、本発明の 定形状メタクリル榭脂重合体と不定形状メタクリル樹脂重合体混合物を 220〜300°C で溶融後、 Tダイを通して板状に押出し、ポリシングロールで表面を仕上げ冷却後、 切断することにより板状体を得ることが出来る。  [0021] The extruded plate of the present invention can be produced by a usual melt extrusion method. For example, a mixture of the regular shape methacrylic resin and the irregular shape methacrylic resin polymer of the present invention is melted at 220 to 300 ° C., then extruded into a plate shape through a T-die, the surface is finished with a polishing roll, cooled, and then cut. A plate-like body can be obtained.
[0022] 板厚精度は、幅 1000mmの板にぉ 、て 50mm間隔で測定した板厚の平均値と測 定点の最大値および最小値との差である。板厚が 2. 0〜15. Ommの場合は板厚精 度が平均板厚の ± 1. 0%以内、好ましくは ±0. 5%以内である。  [0022] The plate thickness accuracy is the difference between the average value of the plate thickness measured at intervals of 50 mm and the maximum and minimum values of the measurement points for a plate having a width of 1000 mm. When the plate thickness is 2.0 to 15. Omm, the plate thickness accuracy is within ± 1.0% of the average plate thickness, preferably within ± 0.5%.
[0023] さらに板厚が 3. 5〜8. 5mmの場合は板厚精度が平均板厚の ±0. 5%以内であ る。  [0023] Further, when the plate thickness is 3.5 to 8.5 mm, the plate thickness accuracy is within ± 0.5% of the average plate thickness.
発明の効果  The invention's effect
[0024] 本発明のメタタリル榭脂押出板は、光源ランプ力も入光した光の発光効率を最大限 に向上させると共に、輝度斑を低減する効果を有する。  [0024] The metathalyl resin extruded plate of the present invention has the effect of maximally improving the light emission efficiency of light that has also entered the light source lamp force and reducing luminance spots.
発明を実施するための最良の形態  BEST MODE FOR CARRYING OUT THE INVENTION
[0025] 本発明を実施例に基づいて説明する。 [0025] The present invention will be described based on examples.
(球状メタタリル榭脂重合体平均粒径の測定方法)  (Measuring method of average particle diameter of spherical metataryl rosin polymer)
電磁振とう式篩分測定器 (三田村理研工業株式会社製電磁振動式 AS200 DISI T)を用いた。試料 lOOgを呼び寸法 500— 425— 355— 300— 250— 150— 150ァ ンダ一の 7段力もなる篩の最上段篩上に乗せ、シーブシェーカーにて 10分間振とう 後、各篩上の球状メタタリル榭脂重合体を量り、累積残留分布曲線を書き、メジアン 径を求め、平均粒径とした。平均粒径の小さな重合体用には呼び寸法 300— 250— 180— 125— 100— 63— 63アンダーの 7段からなる篩を用いて測定した。  An electromagnetic shaking sieving meter (electromagnetic vibration AS200 DISIT manufactured by Mitamura Riken Kogyo Co., Ltd.) was used. Sample lOOg is placed on top of the 7-stage sieve of the size 500-425-355-300-250-150-150, and shaken with a sieve shaker for 10 minutes, then spherical on each sieve. The metataryl rosin polymer was weighed, a cumulative residual distribution curve was written, the median diameter was determined, and the average particle diameter was obtained. For polymers with a small average particle size, measurements were made using a seven-stage sieve with a nominal size of 300-250-180-125-100-63-63.
(円柱状メタクリル榭脂重合体の長径、短径、長さの測定方法) 外側マイクロメータ (株式会社ミツトヨ製 MDC— 25M) )を用い、試料 200粒の長径 、短径、長さを 0. OOlmmまで測定し、その平均値を求めた。 (Measurement method of major axis, minor axis, length of cylindrical methacrylic resin) Using an outer micrometer (MDC-25M manufactured by Mitutoyo Corporation), the major axis, minor axis, and length of 200 samples were measured up to 0.00 lmm, and the average value was determined.
(扁平状メタクリル榭脂重合体の長径、短径、長さの測定方法)  (Measurement method of major axis, minor axis and length of flat methacrylic resin)
外側マイクロメータ (株式会社ミツトヨ製 MDC— 25M) )を用い、試料 200粒の長径 、短径、厚さを 0. 001mmまで測定し、その平均値を求めた。  Using an outer micrometer (MDC-25M manufactured by Mitutoyo Corporation), the major axis, minor axis, and thickness of 200 samples were measured up to 0.001 mm, and the average value was obtained.
(見掛け密度)  (Apparent density)
JIS K 7365に準じて測定した。  Measured according to JIS K 7365.
(メタクリル榭脂押出板の厚み測定)  (Measurement of thickness of methacrylic resin extruded plate)
図 1に示した幅 1000mmの板において 50mm間隔で 19点外側マイクロメータ(株 式会社ミツトヨ製 MDC— 25M) )を用い 0. OOlmmまで測定した。各測定点の平均 値を求め、該平均値と各測定点の最大値、最小値とから板厚精度を算出した。最大 厚みの板厚精度を「板厚精度 A」、最小厚みの板厚精度を「板厚精度 B」とした。  Using a 1000 mm wide plate shown in Fig. 1, measurements were made up to 0.00 lmm using a 19 point outside micrometer (MDC-25M manufactured by Mitutoyo Corporation) at 50 mm intervals. The average value of each measurement point was determined, and the plate thickness accuracy was calculated from the average value and the maximum value and minimum value of each measurement point. The plate thickness accuracy of the maximum thickness is “plate thickness accuracy A”, and the plate thickness accuracy of the minimum thickness is “plate thickness accuracy B”.
板厚精度— A(%) = (最大値—平均値) Z平均値 X 100· · · (1)  Thickness accuracy—A (%) = (Maximum value—Average value) Z Average value X 100 (1)
板厚精度 B (%) = (最小値 平均値) Z平均値 X 100· · · (2)  Sheet thickness accuracy B (%) = (Minimum value average value) Z Average value X 100 (2)
[0026] (導光板の輝度、輝度斑の測定方法) [0026] (Measurement method of brightness of light guide plate, brightness spot)
図 2に示した光源装置に準じ、光源として 3mm φの冷陰極管 (ハリソン電気製)を 導光板の長さ 319mm側の両端面に設置し、光反射シートとしてレイホワイト 75 (きも と製)を用い、導光板の上部に光拡散シート D121 (ッジデン製)を 2枚載せた。冷陰 極管には直流電圧安定装置より 12Vの電圧をかけ 20分間点灯後に発光面から lm 離れた位置に設置した輝度計 (CA— 1000 :ミノルタ製)により、発光面全体を縦 19 X横 19 = 361分割した測定点の各々の輝度を測定した。次 、で得られた 361点の 測定値から平均輝度を算出した。また、得られた 361点の測定値から下記式 (3)によ り輝度斑の評価指標として均斉度を算出した。  In accordance with the light source device shown in Fig. 2, a cold cathode tube of 3mmφ (made by Harrison Electric Co., Ltd.) is installed as a light source on both end faces of the light guide plate at the length of 319mm, and Ray White 75 (made by Kimoto) is used as a light reflecting sheet. And two light diffusion sheets D121 (made by Gidden) were placed on the top of the light guide plate. The cold cathode tube was charged with a voltage of 12V from a DC voltage stabilizer and lit for 20 minutes after being lit for 20 minutes. The luminance meter (CA-1000: manufactured by Minolta) installed at a position distant from the light emitting surface vertically 19 X horizontal The luminance of each of the measurement points divided into 19 = 361 was measured. Next, the average luminance was calculated from the 361 measured values obtained in the above. Also, the uniformity was calculated from the obtained 361 measured values as an evaluation index of luminance spots by the following formula (3).
輝度均斉度(%) =最小輝度値 Z最大輝度値 X 100· · · (3)  Luminance uniformity (%) = Minimum luminance value Z Maximum luminance value X 100 (3)
[0027] (球状メタタリル榭脂重合体 (重合体— A)の製造) [0027] (Production of Spherical Metataryl Resin Polymer (Polymer—A))
メタクリル酸メチル 95. 0重量部、アクリル酸メチル 5. 0重量部、ラウロイルパーォキ サイド 0. 15重量部、 n—ォクチルメルカプタン 0. 25重量部、脱イオン水 130重量部 、水酸ィ匕アルミニウム 0. 65重量部を 200リットルの重合機に投入し、攪拌混合した。 反応温度 80°Cで 150分懸濁重合し、続いて 100°Cで 60分熟成し重合反応を実質 終了した。次ぎに重合反応液を 50°Cまで冷却し、希硫酸を投入し、洗浄脱水乾燥処 理し、メルトフローレイト(ISO— 1139— Condl3) l. OgZlO分の球状メタクリル榭 脂重合体 (重合体— A)を得た。重合体— Aの平均粒径は 0. 39mm,見掛け密度は 0. 76gZmlであった。 95.0 parts by weight of methyl methacrylate, 5.0 parts by weight of methyl acrylate, 0.15 parts by weight of lauroyl peroxide, 0.25 parts by weight of n-octyl mercaptan, 130 parts by weight of deionized water, 00.65 parts by weight of aluminum was put into a 200-liter polymerization machine and mixed with stirring. Suspension polymerization was carried out at a reaction temperature of 80 ° C for 150 minutes, followed by aging at 100 ° C for 60 minutes to complete the polymerization reaction. Next, the polymerization reaction solution was cooled to 50 ° C, diluted sulfuric acid was added, washed and dehydrated and dried, and melt flow rate (ISO-1139—Condl3) l. OgZlO-containing spherical methacrylic resin (polymer) — I got A). Polymer-A had an average particle size of 0.39 mm and an apparent density of 0.76 gZml.
(円柱状メタクリル榭脂重合体 (重合体— B)の製造)  (Manufacture of cylindrical methacrylic resin (polymer B))
メタクリル酸メチル 79. 9重量%、アクリル酸メチル 5. 1重量%、及びェチルベンゼ ン 15重量%カもなる単量体混合物に 1, 1—ビス(t—ブチルパーォキシ)—3, 3, 5 ートリメチルシクロへキサン 150ppm及び n—ォクチルメルカプタン 300ppm 添加し、完全混合型重合反応機で重合温度 155°C、滞留時間 2. 0時間、重合転ィ匕 率 53%まで連続的に重合する。重合液を連続的に重合反応機から取出し、次いで 加熱板で 260°Cに加熱し、加熱版の間隔を通して流延落下させた。脱揮タンク、 2. 7kPa、 230°Cに維持し、重合体と未反応単量体及び溶剤とを分離した。重合体は押 出機に連続的に溶融状態で移送し、押出機を通してダイスよりストランド状に押出さ れ、水冷 (水温度 60°Cのバス)し、ストランドカッターで切断され、メルトフローレイト (I SO 1139 Condi 3) 1. OgZ 10分の円柱状メタクリル榭脂重合体 (重合体— B)を得 た。重合体—Bの長径 (al)、短径 (bl)、長さ(L)は、それぞれ (al) 2. 773mm, (bl) 2. 689mm, (L) 3. 105mm, (bl) / (al) 0. 97、見掛け密度は 0. 67gZmlであつ た。  1,1-bis (t-butylperoxy) -3,3,5-trimethyl in a monomer mixture consisting of 79.9% by weight methyl methacrylate, 5.1% by weight methyl acrylate, and 15% by weight ethylbenzen 150 ppm of cyclohexane and 300 ppm of n-octyl mercaptan are added, and polymerization is continuously carried out to a polymerization temperature of 155 ° C, a residence time of 2.0 hours, and a polymerization conversion rate of 53% in a fully mixed polymerization reactor. The polymerization solution was continuously taken out from the polymerization reactor, then heated to 260 ° C with a heating plate, and cast and dropped through the space between the heating plates. A devolatilization tank, maintained at 2.7 kPa, 230 ° C, separated the polymer from unreacted monomers and solvent. The polymer is continuously transferred to the extruder in a molten state, extruded through the extruder into a strand from a die, water-cooled (water temperature: 60 ° C bath), cut with a strand cutter, and melt flow rate ( I SO 1139 Condi 3) 1. A 10-minute cylindrical methacrylic resin (polymer B) was obtained. The major axis (al), minor axis (bl), and length (L) of polymer—B are (al) 2. 773mm, (bl) 2. 689mm, (L) 3. 105mm, (bl) / ( al) It was 0.97 and the apparent density was 0.67 gZml.
(扁平状メタクリル榭脂重合体 (重合体— C)の製造)  (Manufacture of flat methacrylic resin (polymer C))
重合体 Bの製造工程でダイスよりストランド状に押出し、水冷後カッターで切断す る代わりに、ダイスより水中に押出し切断するアンダーウォーターカット方式で切断し 、メルトフローレイ HISO— 1139— Condl3) l. OgZ 10分の扁平状メタクリル榭脂 重合体 (重合体— C)を得た。重合体— Dの長径 (a2)、短径 (b2)、厚さ (T)は、それ ぞれ(a2) 3. 178mm, (b2) 3. 089mm, (T) l. 505mm, (b2) / (a2) 0. 97、見掛 け密度は 0. 68g/mlであった。  In the production process of polymer B, instead of extruding into a strand from a die and then cooling with water and then cutting with a cutter, it is cut with an underwater cut method that extrudes and cuts into water from a die, and melt flowlay HISO-1139—Condl3) l. A flat methacrylic resin (polymer C) with OgZ of 10 minutes was obtained. Polymer — D major axis (a2), minor axis (b2), thickness (T) are (a2) 3. 178mm, (b2) 3. 089mm, (T) l. 505mm, (b2) / (a2) 0.97, apparent density 0.668 g / ml.
(不定形状メタタリル榭脂重合体 (重合体 D)の製造) (Manufacture of amorphous metataryl rosin polymer (Polymer D))
重合体— Aを用いシート用 Tダイ (ダイ温度: 250°C)を有する 150mm φ単軸押出 機(シリンダ温度:フィード側より 200°C -210°C -210°C - 260°C - 260°C - 240 °C) )と温調された 3本ポリシンダロール (ロール温度: 80°C)と引取り装置からなる押 出シート成形機を用い、押出量 600KgZhrで押出し、幅 1000mm、厚み 6mmのメ タクリル榭脂押出板を得た。次ぎにこの押出板を株式会社ホーライ製粉砕機 (U10 — 30120XLFX型)(スクリーン: 10mm φ )を用いて粉砕し、不定形状メタタリル榭脂 重合体 (重合体— D)を得た。重合体— Dの見掛け密度は 0. 60gZmlであった。 実施例 1 Polymer — 150mm φ single screw extrusion with A and T die for sheet (die temperature: 250 ° C) Machine (cylinder temperature: 200 ° C -210 ° C -210 ° C -260 ° C -260 ° C -240 ° C) from the feed side) and three poly cinder rolls (roll temperature: 80 ° C) ) And an extrusion sheet forming machine comprising a take-up device, and extruded with a extrusion amount of 600 kgZhr to obtain a methacrylic resin extruded plate having a width of 1000 mm and a thickness of 6 mm. Next, this extruded plate was pulverized by using a pulverizer (U10-30120XLFX type) (screen: 10 mmφ) manufactured by Horai Co., Ltd. to obtain an irregular-shaped metataryl rosin polymer (polymer D). The apparent density of Polymer-D was 0.60 gZml. Example 1
[0028] 重合体 A100重量部と重合体 D50重量部との混合物(見掛け密度 0. 83g/ ml)をシート用 Tダイ (ダイ温度: 250°C)を有する 150mm φ単軸押出機 (シリンダ温 度:フィード側より 200°C -210°C -210°C - 260°C - 260°C - 240°C) )と温調され た 3本ポリシンダロール (ロール温度: 80°C)と引取り装置力 なる押出シート成形機 を用い、押出量 600KgZhrで押出し、幅 1000mm、厚み 6mmのメタクリル榭脂押 出板 (押出板— A)を得た。図 1で示した厚み測定点について測定し、板厚精度を算 出した結果を表 1に示す。  [0028] 150 mm φ single screw extruder (cylinder temperature) with T die (die temperature: 250 ° C) for sheet (mixture of 100 parts by weight of polymer A and 50 parts by weight of polymer D (apparent density 0.83 g / ml)) Degree: 200 ° C -210 ° C -210 ° C -260 ° C -260 ° C -240 ° C))) and 3 poly cinder rolls (roll temperature: 80 ° C) A methacrylic resin extruded plate (extruded plate-A) having a width of 1000 mm and a thickness of 6 mm was obtained by extrusion using an extrusion sheet molding machine having a removing device strength and an extrusion amount of 600 kgZhr. Table 1 shows the results of measuring the thickness measurement points shown in Fig. 1 and calculating the plate thickness accuracy.
次いで得られた押出板から幅 241mm、長さ 319mmのサイズに丸鋸を用いて切り 出し、切り出した板のカット面を精密研磨機 (PLA— BEAUTY:メガロテク-力 (株) 製)を用いて研磨し、更にパフ研磨を施し鏡面状に仕上げる。次いで、 15インチサイ ズのドットグラデーションを施した印刷スクリーンを用い、インクにマットメジゥム SR93 1 (ミノグループ製)を使用して、導光板の片面にスクリーン印刷行い導光板を得た。 輝度、輝度斑の測定結果を表 1に示す。  Next, the resulting extruded plate was cut into a size of 241 mm in width and 319 mm in length using a circular saw, and the cut surface of the cut plate was cut using a precision polishing machine (PLA—Beauty: manufactured by Megalotech-Power Co., Ltd.). Polish and then puffed to give a mirror finish. Next, using a printing screen having a 15-inch size dot gradation and using Mattmedium SR931 (Mino Group) as ink, screen printing was performed on one side of the light guide plate to obtain a light guide plate. Table 1 shows the measurement results of luminance and luminance spots.
実施例 2  Example 2
[0029] 実施例 1で用いた重合体 Dの配合量を 100重量部とした混合物(見掛け密度 0.  [0029] A mixture in which the blending amount of the polymer D used in Example 1 was 100 parts by weight (apparent density 0.
88g/ml)にする以外、実施例 1と同様にして押出板— Bを得た。実施例 1と同様に 厚み測定、輝度、輝度斑の測定を行い、結果を表 1に示す。  Extruded plate B was obtained in the same manner as in Example 1 except that the amount was 88 g / ml). As in Example 1, thickness measurement, brightness, and brightness spots were measured, and the results are shown in Table 1.
<比較例 1 >  <Comparative Example 1>
実施例 1で用いた重合体—Dの配合量を 400重量部とした混合物(見掛け密度 0. 75g/ml)にする以外、実施例 1と同様にして押出板— Cを得た。実施例 1と同様に 厚み測定、輝度、輝度斑の測定を行い、結果を表 1に示す。 <比較例 2, 3 > Extruded plate C was obtained in the same manner as in Example 1 except that the mixture (polymer apparently used in Example 1) had a blending amount of 400 parts by weight (apparent density 0.75 g / ml). As in Example 1, thickness measurement, brightness, and brightness spots were measured, and the results are shown in Table 1. <Comparative Examples 2, 3>
実施例 1で用いた重合体 A (見掛け密度 0. 76gZml)及び重合体 D (見掛け 密度 0. 60gZml)を実施例 1と同様にしてそれぞれ単独で押出し、押出板— D及び 押出板— Eを得た。実施例 1と同様に厚み測定、輝度、輝度斑の測定を行い、結果を 表— 1に示す。  Polymer A (apparent density 0.76 gZml) and polymer D (apparent density 0.60 gZml) used in Example 1 were each extruded in the same manner as in Example 1 and extruded plate D and extruded plate E Obtained. As in Example 1, thickness measurement, luminance, and luminance spots were measured, and the results are shown in Table 1.
実施例 3  Example 3
[0030] 実施例 1で用いた重合体— A100重量部の代わりに重合体— A50重量部、重合体 — B50重量部を用いた混合物(見掛け密度 0. 88gZml)にする以外、実施例 1と同 様にして押出板— Fを得た。実施例 1と同様に厚み測定、輝度、輝度斑の測定を行 い、結果を表 1に示す。  [0030] The polymer used in Example 1 was replaced with Example 1 except that the polymer (A50 parts by weight) and the polymer (B50 parts by weight) were used instead of A100 parts by weight. In the same manner, Extruded Plate-F was obtained. As in Example 1, thickness measurement, luminance, and luminance spots were measured, and the results are shown in Table 1.
実施例 4  Example 4
[0031] 実施例 3で用いた重合体 Bの代わりに重合体 Cを用いた混合物(見掛け密度 0 . 87gZml)にする以外、実施例 1と同様にして押出板— Gを得た。実施例 1と同様 に厚み測定、輝度、輝度斑の測定を行い、結果を表 1に示す。  [0031] Extruded plate-G was obtained in the same manner as in Example 1, except that the mixture was changed to a mixture using the polymer C instead of the polymer B used in Example 3 (apparent density 0.87 gZml). As in Example 1, thickness measurement, luminance, and luminance spots were measured, and the results are shown in Table 1.
実施例 5  Example 5
[0032] 実施例 1の押出原料を用 、て板厚 8mmのメタクリル榭脂押出板 (押出板 H)を成 型し、実施例 1と同様に厚み測定、輝度、輝度斑の測定を行い、結果を表— 1に示す  [0032] Using the extruded raw material of Example 1, a methacrylic resin extruded plate (extruded plate H) having a thickness of 8 mm was formed, and in the same manner as in Example 1, thickness measurement, luminance, and luminance unevenness were measured. The results are shown in Table 1
(結果の概要) (Summary of results)
実施例 1〜5の輝度、輝度斑共に比較例 1〜3に比べ優れた性能を発現した。  The brightness | luminance of Example 1-5 and the brightness spot expressed the performance outstanding compared with Comparative Examples 1-3.
[0033] [表 1] [0033] [Table 1]
重合体(重量部) 押出板 平均板羅 最大板 JS 板 S精度- A 最小板厚 板厚精度- B 平均輝度 輝度均斉度Polymer (parts by weight) Extruded plate Average plate Max plate JS plate S accuracy-A Minimum plate thickness Accuracy-B Average brightness Brightness uniformity
A B C D 5, mm) (mm) (%) imm) 《%) (cd/m2) (%) 実施倒 1 100 0 0 50 6, 030 6.045 + 0.25 6.010 -0.33 2935 82 実施倒 2 100 0 0 100 押出板一 B 6.015 6, 036 +0.35 5.997 -0.30 2928 81 比較例 1 100 0 0 400 押出板一 G 6.008 6.084 +1.26 5.930 —1.30 2795 72 比較例 2 100 0 0 0 押出板一 D 6.006 6.078 +1.20 5.927 -1.32 2790 73 比較例 3 0 0 0 100 押出板一 E 6.000 + 2. 17 5.890 -1.83 2680 70 実施例 3 50 50 0 50 押出板一 F 6.001 6.019 +0.30 S.982 ~0.32 2928 83 実施例 4 50 0 50 50 押出板一 G 5.997 6.020 +0.38 5.977 -0.33 2920 81 実施例 5 100 0 0 50 押出板一 H 8.010 8.032 +0.27 7.995 —0. 19 2950 " ο ABCD 5, mm) (mm) (%) imm) 《%) (cd / m 2 ) (%) Implemented 1 100 0 0 50 6, 030 6.045 + 0.25 6.010 -0.33 2935 82 Implemented 2 100 0 0 100 Extrusion plate B 6.015 6, 036 +0.35 5.997 -0.30 2928 81 Comparative example 1 100 0 0 400 Extrusion plate G 6.008 6.084 +1.26 5.930 —1.30 2795 72 Comparative example 2 100 0 0 0 Extrusion plate D 6.006 6.078 +1.20 5.927 -1.32 2790 73 Comparative example 3 0 0 0 100 Extrusion plate E 6.000 + 2. 17 5.890 -1.83 2680 70 Example 3 50 50 0 50 Extrusion plate F 6.001 6.019 +0.30 S.982 to 0.32 2928 83 Example 4 50 0 50 50 Extruded plate G 5.997 6.020 +0.38 5.977 -0.33 2920 81 Example 5 100 0 0 50 Extruded plate H 8.010 8.032 +0.27 7.995 —0. 19 2950 "ο
産業上の利用可能性 Industrial applicability
[0034] 本発明の導光板は、パーソナルコンピュータやワードプロセッサなどのオフィスォー トメーシヨン機器、画像信号を表示する各種モニター、例えばパネルモニター、テレビ モニター等に用いられる表示装置及び室内外空間の照明装置に使用される表示装 置や看板等に好適に利用できる。  [0034] The light guide plate of the present invention is used in office automation equipment such as personal computers and word processors, various monitors for displaying image signals, for example, display devices used for panel monitors, television monitors and the like, and lighting devices for indoor and outdoor spaces. It can be suitably used for display devices and signboards.
図面の簡単な説明  Brief Description of Drawings
[0035] [図 1]本発明における厚み測定点を示したものである。 [0035] [Fig. 1] Shows thickness measurement points in the present invention.
[図 2]本発明の導光板を用いたエッジライト方式液晶光源装置での輝度評価方法の 一例を示したものである。  FIG. 2 shows an example of a luminance evaluation method in an edge light type liquid crystal light source device using the light guide plate of the present invention.
符号の説明  Explanation of symbols
[0036] A:光源 (冷陰極管) [0036] A: Light source (cold cathode tube)
B :ランプハウス  B: Lamp house
C :導光板  C: Light guide plate
D :光反射シート  D: Light reflection sheet
E :光拡散シート  E: Light diffusion sheet

Claims

請求の範囲 The scope of the claims
[1] 見掛け密度 0. 63gZml〜0. 78gZmlの定形状メタクリル榭脂重合体と見掛け密 度 0. 55gZml〜0. 63gZmlの不定形状メタクリル樹脂重合体とを見掛け密度が 0. 80g/ml以上となるように混合し、得られた混合物を押出し成形して、板厚が 2. 0〜 15. Ommであって、幅方向の板厚精度が平均板厚の ± 1. 0%以内である導光板用 メタタリル榭脂押出板を製造する方法。  [1] Apparent density between 0.663 gZml to 0.78 gZml of fixed-form methacrylic resin and apparent density between 0.55 gZml to 0.63 gZml of amorphous methacrylic resin polymer with an apparent density of at least 0.80 g / ml The resulting mixture is extruded to obtain a sheet thickness of 2.0 to 15. Omm, and the sheet thickness accuracy in the width direction is within ± 1.0% of the average sheet thickness. A method for producing a metathalyl resin extruded plate for optical plates.
[2] 該板厚が 3. 5〜8. 5mmであり、且つ幅方向の板厚精度が平均板厚の ±0. 5% 以内であることを特徴とする、請求項 1記載の導光板用メタクリル榭脂押出板の製造 方法。  [2] The light guide plate according to claim 1, wherein the plate thickness is 3.5 to 8.5 mm, and the plate thickness accuracy in the width direction is within ± 0.5% of the average plate thickness. For producing a methacrylic resin extruded plate.
[3] 請求項 1または請求項 2記載の方法で製造した導光板用メタクリル榭脂押出板。  [3] A methacrylic resin extruded plate for a light guide plate produced by the method according to claim 1 or claim 2.
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