WO2006054510A1 - Resin extruded plate for optical use and method for manufacturing same - Google Patents

Resin extruded plate for optical use and method for manufacturing same Download PDF

Info

Publication number
WO2006054510A1
WO2006054510A1 PCT/JP2005/020819 JP2005020819W WO2006054510A1 WO 2006054510 A1 WO2006054510 A1 WO 2006054510A1 JP 2005020819 W JP2005020819 W JP 2005020819W WO 2006054510 A1 WO2006054510 A1 WO 2006054510A1
Authority
WO
WIPO (PCT)
Prior art keywords
resin
plate
extruded
polymerization
resin extruded
Prior art date
Application number
PCT/JP2005/020819
Other languages
French (fr)
Japanese (ja)
Inventor
Yoshikazu Tsuruta
Shunji Kamiya
Original Assignee
Asahi Kasei Chemicals Corporation
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Asahi Kasei Chemicals Corporation filed Critical Asahi Kasei Chemicals Corporation
Priority to JP2006545003A priority Critical patent/JPWO2006054510A1/en
Publication of WO2006054510A1 publication Critical patent/WO2006054510A1/en

Links

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
    • 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
    • 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
    • B29C48/08Flat, e.g. panels flexible, e.g. films
    • 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
    • B29C48/16Articles comprising two or more components, e.g. co-extruded layers

Definitions

  • the present invention relates to a liquid crystal display used as a display device such as a notebook or desktop personal computer, a portable information terminal, a game machine, a workstation, an image monitor, or a television, and also illuminates the liquid crystal with a back force.
  • the present invention relates to a resin extruded plate suitable for a light guide plate used in a backlight device.
  • the present invention relates to a method for producing a resin extruded plate suitable for a light guide plate suitable for producing a backlight device that does not impair the luminance and image quality of a liquid crystal display.
  • CRTs so-called CRTs
  • V a so-called knock light device
  • Japanese Patent Publication No. 39-1194 discloses a light guide plate.
  • JP-A-4-145485 discloses a method for obtaining a uniform light emitting surface by dispersing and mixing light diffusing particles. By using a light-scattering plastic material including fine particles having different refractive indexes as a light guide. Although a method for increasing the brightness is disclosed, the process is complicated.
  • 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.
  • a resin extruded plate for a light guide plate is generally a saw blade in order to have a predetermined width and length after a surface protective film is attached to the front and back so that the surface of the plate is not scratched. Because it is cut with, it is easy for the chips to adhere to the surface protection film.
  • the produced resin extrusion board is loaded on a pallet and stored and transported. As a result, the chips adhering to the surface protection film are pressed by the weight of the stacked plates, causing dents on the surface of the plates, and in severe cases, breaking the surface protection film and causing scratches on the surface of the plates. Cause.
  • the chips on the board are likely to damage the surface protection film due to the shaking of the ship being transported, and the surface of the board tends to be dented or damaged.
  • the method of cutting a resin extruded plate that does not generate chips is as follows: 1) Shear cutting machine that cuts the blade by pressing one side or both sides of the plate, 2) A device that cuts with a laser beam, 3 ) A device that cuts with a water jet.
  • All of these devices require a large force if the equipment is large and expensive.
  • Shear cutting machines have a large running cost due to blunting of the blades and immediate replacement of the blades.
  • Patent Document 1 Japanese Patent Publication No. 39-1194
  • Patent Document 2 JP-A-4-145485
  • An object of the present invention is to provide a resin-extruded plate suitable for a light guide plate of a high-luminance edge light type backlight device for a liquid crystal display and having no chip adhesion.
  • a surface protective film is applied to the front and back of a plate having a plate thickness of 2 to 15 mm.
  • the resin extruded plate of the present invention can maximize the luminous efficiency of the light incident upon the light source lamp force with no bright spots derived from chip adhesion.
  • FIG. 1 shows an example of a chip suction rotary brush according to the present invention.
  • FIG. 2 shows thickness measurement points in the present invention.
  • FIG. 3 shows an example of a bright spot evaluation method in an edge light type liquid crystal light source device using the light guide plate of the present invention.
  • FIG. 4 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.
  • FIG. 5 shows an example of a production facility for a resin extruded plate according to the present invention.
  • the resin-extruded plate of the present invention can be produced by melt-extruding a raw material resin to form a plate.
  • Raw material resin includes methacrylic resin (PMMA), polystyrene (PS), styrene Z-methylmethalate resin (MS), acrylonitrile Z styrene resin (SAN), polycarbonate (PC), amorphous polyester Any alicyclic polyolefin (such as Mitsui Petrochemical's APO, Nippon Zeon's ZEONEX and ZEONOR, JSR's ARTON, etc.) can be used as long as it is transparent and melt-moldable.
  • Mitsui Petrochemical's APO such as Mitsui Petrochemical's APO, Nippon Zeon's ZEONEX and ZEONOR, JSR's ARTON, etc.
  • the plate may be produced by extruding as a single layer, or may be laminated into two or more layers by a coextrusion method or a laminating method.
  • methallyl resin is suitable as a raw material for the light guide plate in terms of transparency.
  • methacrylic resin is colorless and transparent, light resistance, molding processability In view of properties such as mechanical strength and surface hardness, it is particularly preferably used.
  • the methacrylic resin that can be used particularly preferably in the present invention is, for example, 70% by weight or more of methyl methacrylate and Z or ethyl methacrylate, and less than 30% by weight of monomers having copolymerizability with these. Can be obtained by copolymerization.
  • the copolymerizable monomer include propyl methacrylate, butyl methacrylate, cyclohexyl methacrylate, 2-ethylhexyl methacrylate, tricyclodecyl methacrylate, phenol, methacrylate, and methacrylic acid.
  • Methacrylic acid esters such as benzyl, methyl acrylate, acrylic Acrylate esters such as ethyl acid, propyl acrylate, butyl acrylate, cyclohexyl acrylate, 2-ethylhexyl acrylate, tricyclodecyl acrylate, acrylic acid phenyl, benzyl acrylate, methacrylic acid Powers including unsaturated acids such as acid and acrylic acid, maleic anhydride, maleimide and the like are not limited to these. These monomers may be used alone or in combination of two or more.
  • the resin used as the raw material for the resin extruded board according to the present invention can be obtained by any polymerization method such as suspension polymerization, emulsion polymerization, cast polymerization, continuous bulk polymerization, and continuous solution polymerization. Can also be used.
  • a resin manufactured using a suspension polymerization method and a continuous solution polymerization method, particularly a methallyl resin, is preferable as a raw material resin for a light guide plate with less interstitial material.
  • a suspension polymerization method of a methacrylic resin as an example of a raw material will be described.
  • a polymerization initiator and a chain transfer agent are uniformly dissolved in a monomer mixture composed of methyl metatalate and Z or ethyl methacrylate and another copolymerizable 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. Can be obtained.
  • Examples of the polymerization initiator used in suspension polymerization include radical polymerization initiators known for polymerization of vinyl monomers. For example, azobisisobutyl-tolyl, 2,2,1azobis (2,4 dimethylvaleronitrile), dimethyl-1,2,2'-azobisisobutyrate, t-butyl peroxypivalate, t-butyl peroxy 2- Examples include ethinorehexaate, tamperoxy 2-ethyl hexanoate, benzoyl peroxide, lauryl peroxide, and the like.
  • the amount of these polymerization initiators used is preferably in the range 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 known one used for the polymerization of methyl methacrylate. Examples thereof include t-butyl mercaptan, n-butyl mercaptan, n-octyl mercaptan, t-dodecyl mercaptan and the like.
  • 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, but is a poorly water-soluble inorganic compound such as calcium phosphate, calcium carbonate, aluminum hydroxide or the like, polybutyl alcohol, polyethylene oxide, cellulose.
  • Nonionic polymer compounds such as derivatives, polyacrylic acid and its salts, polymethacrylic acid and its salts, copolymer of methacrylic acid ester and methacrylic acid and its salts, etc. I can do it.
  • 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.
  • Examples of water used in suspension polymerization include pure water, ion-exchanged water, and deionized water.
  • the amount of water used is not particularly limited, but is preferably in the range of 100 to 300 parts by weight per 100 parts by weight of the monomer or monomer mixture! /.
  • the polymerization temperature of the suspension polymerization is not particularly limited, but is about 60 to 120 ° C and a temperature 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 light diffusing agent an ultraviolet absorber, a fluorescent whitening agent, an antioxidant, a plasticizer, a release agent, a dye, a pigment, and the like may be suspended and polymerized.
  • a spherical resin for example, a spherical methallyl resin
  • washing, dehydrating and drying by a known method.
  • the average particle size of the spherical resin used as a raw material for the resin extruded plate according to the present invention is 0.2 to 0.5 mm, and preferably 0.25 to 0.39 mm. If it is less than 0.2 mm, good plate thickness accuracy cannot be obtained, and it is difficult to stably produce a polymer having an average particle diameter exceeding 0.5 mm.
  • the resin used as a raw material for the resin extruded plate in the present invention is a spherical resin obtained by suspension polymerization, and a spherical resin is supplied to an extruder equipped with a vent at a temperature of 220 to 260 ° C. Vent vacuum pressure of 10-60 torr.
  • Extruded into strands from extrusion dies, cooled with water, cut into strand cutters (pellet-shaped), and known continuous solution polymerization method, continuous mass Use a cylindrical (pellet-shaped) resin obtained by extruding a molten resin polymer obtained by a state polymerization method into a strand from an extrusion die, water-cooling, and cutting with a strand cutter.
  • the Examples of the continuous solution polymerization method and the continuous bulk polymerization method include the following methods.
  • a monomer of a raw material resin for example, a monomer capable of copolymerizing with a methyl methacrylate monomer, a methyl methacrylate monomer, and a methyl methacrylate at the bottom of the distillation column and inside the distillation column.
  • aromatic compounds such as toluene, xylene, ethylbenzene, and jetylbenzene, aliphatic compounds such as octane and decane, alicyclic compounds such as decalin, acetic acid, etc.
  • esters such as butyl and pentyl acetate, and halogen compounds such as 1, 1, 2, 2-tetrachloroethane.
  • alkylbenzene and among them, toluene, xylene and ethylbenzene are preferable because they have appropriate boiling points, have less degassing load and do not adversely affect polymerization.
  • the amount of the solvent varies depending on the boiling point of the solvent.
  • the amount of the solvent is preferably 30% by weight or less, more preferably 25% by weight or less based on the weight of the total mixture at the time of polymerization. If no solvent is used during polymerization, bulk polymerization occurs.
  • the polymerization initiator used in the continuous solution polymerization method and the continuous bulk polymerization method can be a polymerization initiator that decomposes actively at the polymerization temperature to generate radicals.
  • a polymerization initiator that decomposes actively at the polymerization temperature to generate radicals.
  • di-t-butyl peroxide dicumyl peroxide, methyl ethyl ketone peroxide, di-t-butyl perphthalate, di-t-butyl perbenzoate, t-butyl peracetate, 2,5-dimethyl-2,5-di (t —Butylperoxy) hexane, 1,1bis (t-butylperoxy) (3,3,5 trimethyl) cyclohexane, 1,1-bis (t-butylperoxy) cyclohexane, di-tamilperoxide, Benzyl peroxide, cumene hydride peroxyside, lauryl peroxide,
  • 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.
  • 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.
  • the polymerization reactor uses a device that is uniformly stirred by a stirring blade such as a double helical ribbon or a pitched paddle type.
  • a stirring blade such as a double helical ribbon or a 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. If the polymerization conversion rate is less than 40%, the load of the devolatilization process due to the volatile component is large. For example, the devolatilization may become insufficient due to the restriction of the heat transfer area of the preheater.
  • the polymerization reaction power is not preferable because the piping pressure loss between the preheaters becomes large and the transport of the polymerization liquid becomes difficult. If the polymerization temperature is less than 120 ° C, the polymerization rate is too slow to be practical, and if it exceeds 160 ° C, the polymerization rate is too high and it is difficult to adjust the polymerization conversion. Further, the heat degradability is lowered, which is not preferable.
  • 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, etc. are used.
  • the polymerization liquid is heated 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, 20 to: LOO Torr temperature, under vacuum Feed the devolatilization tank to remove 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.
  • a light diffusing agent an ultraviolet absorber, a fluorescent whitening agent, an antioxidant, a plasticizer , Mold release agents, dyes, pigments and the like may be added.
  • the resin extruded plate of the present invention can be produced by a melt extrusion molding method. For example, raw resin is melted in an extruder, extruded from T-Dieka, and passed through three, four to five temperature controlled rolls, and formed into a plate shape (preferably a flat plate shape). The molded plate is cooled and solidified while being drawn with a take-up roll through a guide roll, and a resin extruded plate can be obtained as a single-wafer product by cutting the width direction and the flow direction into predetermined lengths. it can.
  • the force capable of producing a resin extruded plate having a desired thickness by adjusting the gap between the polishing rolls and the take-off speed Generally, a resin extruded plate having a thickness of 2 to 15 mm is used for the light guide plate.
  • the present inventors cut the resin extrusion plate with a saw, and then suck the chips while brushing the surface protective film with a rotating brush. We have found that removal is extremely effective.
  • the rotating brush is brought into contact with the surface protective film of the resin extruded plate.
  • the material of the brush filament has moderate elasticity, flexibility and wear resistance, and the surface protective film. There is no particular limitation as long as it does not hurt or turn off the resin board.
  • synthetic fibers such as polypropylene and nylon
  • natural fibers derived from plants or animals can also be used.
  • the rotation speed is no particular limitation on the rotation speed, but generally it is preferably in the range of 100 to 1000 rpm.
  • the suction device incorporates a rotating brush and sucks immediately after the surface of the plate is brushed to remove chips.
  • the rotating brush and the suction device are installed separately, the effect of the present invention cannot be obtained sufficiently.
  • a suction force of 5 kPa or more is sufficient to remove normal chips.
  • B is a rotating brush
  • C is a resin extrusion plate
  • D is a suction duct
  • an arrow from C indicates an extrusion direction.
  • a surface protective film In order to remove the chips adhering to the surface, it is extremely effective to pass the cut plate between the two upper and lower adhesive rolls to adhere and remove the chips adhering to the surface protective film.
  • the adhesive roll can be used to stick and remove chips by kneading or applying an adhesive material such as ethylene Z vinyl alcohol on the surface of elastic materials such as polyurethane and synthetic rubber. If there is no limit Can be used.
  • the roll 1 for directly adhering to and removing the chips by directly contacting the surface protective film is brought into contact with the roll 1 with 2 more strong adhesive rolls. Move and devise so that the surface of roll 1 is kept clean.
  • the thickness was measured up to 0. Olmm using the outer micrometer (MDC-25M manufactured by Mitutoyo Corporation) as the thickness measurement point 2 in the width direction. Averaged.
  • the thickness of the extruded resin plate 1 in the extrusion direction was measured in the same manner as the plate thickness measurement point 3 at intervals of 50 mm over the length of 1000 mm at both ends of the plate.
  • a cold cathode tube (made by Harrison Electric) with a diameter of 3 mm is installed on one side of the light guide plate C as the light source A in the lamp house B.
  • Ray White 75 (made by Kimoto) is used as the reflective sheet D, and the cold cathode tube is visually observed by applying a voltage of 12 V from a DC voltage stabilizer, and the number of bright spots of 0.1 mm 2 or more is observed. To do. Measure 10 samples and get the average value.
  • a cold-cathode tube of 3mm ⁇ (made by Harrison Electric) is installed on both end faces of the light guide plate C on the length side of 319mm, and the light reflecting sheet D Ray white 75 (manufactured by Kimoto) was used as the light diffusion plate E, and two D121 (manufactured by Gidden) were placed on the light guide plate.
  • the cold cathode tube was charged with a voltage of 12V from a DC voltage stabilizer, and after 20 minutes of lighting, a luminance meter (CA-1000: manufactured by Minolta) placed at a distance of 1 lm from the light emitting surface was used to make the entire light emitting surface 19 X horizontal
  • the obtained measurement power of 361 points also calculated the average luminance.
  • An electromagnetic shaking sieving meter (electromagnetic vibration AS200 DISIT manufactured by Mitamura Riken Kogyo Co., Ltd.) was used. Sample lOOg is placed on the top sieve of 0.5 ⁇ 0.15mm 7-stage force, shaken with a shaker for 10 minutes, and the spherical methacrylic resin polymer on each sieve is weighed, and the cumulative residual distribution curve is obtained. Writing, the median diameter was determined and taken as the average particle diameter.
  • 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 Add 150ppm of cyclohexane and 300ppm of n-octyl mercaptan and polymerize in a fully mixed polymerization reactor at a polymerization temperature of 155 ° C and a residence time of 2.0 hours. The liquid was continuously removed from the polymerization reactor, then heated to 260 ° C. with a heating plate, and cast and dropped through the space between the heating plates.
  • the devolatilization tank was maintained at 30 torr and 230 ° C, and the polymer was separated from the unreacted monomer and solvent.
  • the polymer is continuously transferred to the extruder in a molten state, and is pushed into a strand from the die through the extruder. It is cooled with water (60 ° C water bath) and cut with a strand cutter to obtain a melt flow rate (ISO 1139 Condl3) l.
  • OgZlO-containing cylindrical methacrylic resin (polymer B) It was.
  • Polymer — B's major axis (a), minor axis (b), and length (L) are (a) 2. 773mm, (b) 2. 689mm, (L) 3. 105mm, (b) / ( a) 0.97.
  • a mixture of 50 parts by weight of polymer A and 50 parts by weight of polymer B (total 100 parts by weight) is fed to the raw material hopper in Fig. 4, and the cylinder temperature is 210, 210, 240 in order of the hopper side force to the die side. 250, 260, 260.
  • the temperature around the extrusion line was 49 ° C.
  • a fan and air blowing device are provided above and below the guide roll to cool the front and back of the plate. By adjusting these, the temperature distribution of the center and edges of the plate and the front and back are controlled, and there is little warpage.
  • a fat extrusion board is manufactured.
  • a polyethylene masking (90 microns thick) made of Daio Power Paper for surface protection was pasted on the top and bottom of the board at the take-up roll section, and 7) both ends of the board were cut to a width of 1100 mm with a trimming machine. 8) Cut to 1380mm length with a cross-cut machine to make a single sheet, and then pass through the top and bottom 9) chips suction rotating brush (500rpm, suction force 7kPa), 10) feed to conveyor 11) stacker 13)
  • a predetermined number of sheets were loaded on the pallet 12) as light guide plate products. Defective plates were not stacked on the pallet, and 14) discharged to defective dispensing so that they were not mixed into the product. The plate thickness was measured and found to be 6.00 ⁇ 0.05 mm.
  • a resin extruded plate B was obtained in the same manner as in Example 1 except that the chips were sandwiched between two upper and lower adhesive rolls and the chips were removed by suction without using the chip suction rotating brush.
  • Table 1 shows the measurement results of dents or dents, chips, bright spots and brightness.
  • a resin extruded plate C was obtained in the same manner as in Example 1 except that the chip suction rotary brush was not used and only the front and back sides of the board were sucked with a suction force of 7 kPa.
  • Table 1 shows the measurement results of dents or dents, chips, bright spots and brightness.
  • a resin extruded plate D was obtained in the same manner as in Example 1 except that the chip suction rotating brush was not used and only the front and back of the plate were blown with compressed air.
  • Table 1 shows the measurement results of dents or dents, chips, bright spots and brightness.
  • the resin extruded plate of the present invention is used for a liquid crystal display as a display device such as a notebook or desktop personal computer, a portable information terminal, a game machine, a workstation, an image monitor, or a television. It can be suitably used as a light guide plate used in an illuminating backlight device.

Abstract

Disclosed is a resin extruded plate for light guide plates which is suitable for displays used in office automation equipment such as personal computers and word processors, various monitors for displaying image signals such as panel monitors and television monitors as well as displays or advertising displays used in illuminating devices for indoor or outdoor spaces. Specifically disclosed is a resin extruded plate which is characterized in that it comprises surface protection films bonded to both sides of a plate having a thickness of 2-15 mm, there is no cutting dust having a size of 0.1 mm2 or more on the films, and there is no recess and/or dent having a size of 0.1 mm2 or more in the plate surface. Also disclosed is a method for manufacturing such a resin extruded plate.

Description

明 細 書  Specification
光学用樹脂押出板およびその製造方法  Optical resin extrusion plate and manufacturing method thereof
技術分野  Technical field
[0001] 本発明は、ノートブック型またはデスクトップ型のパーソナルコンピュータ、携帯情報 端末、ゲーム機、ワークステーション、画像モニター、あるいはテレビ等の表示装置と して用いられる液晶ディスプレイにおいて、液晶を背面力も照らすバックライト装置に 用いられる導光板に適した榭脂押出板に関する。さらに本発明は、液晶ディスプレイ の輝度や画質を損なわないバックライト装置を作製するのに好適な導光板に適した 榭脂押出板の製造方法に関する。  [0001] The present invention relates to a liquid crystal display used as a display device such as a notebook or desktop personal computer, a portable information terminal, a game machine, a workstation, an image monitor, or a television, and also illuminates the liquid crystal with a back force. The present invention relates to a resin extruded plate suitable for a light guide plate used in a backlight device. Furthermore, the present invention relates to a method for producing a resin extruded plate suitable for a light guide plate suitable for producing a backlight device that does not impair the luminance and image quality of a liquid crystal display.
背景技術  Background art
[0002] 情報および画像の表示装置としては CRT、いわゆるブラウン管が長く用いられてき ている。近年、表示装置の薄型化や小型化の要請に対応して、液晶ディスプレイが ブラウン管を代替していく傾向が見られる。液晶ディスプレイにおいて、液晶ユニット 自体は発光する機能が無いので、一般的には液晶ユニットを背面力 照らして表示 を視認しゃすくする、 V、わゆるノ ックライト装置が用いられて ヽる。  [0002] CRTs, so-called CRTs, have long been used as information and image display devices. In recent years, there has been a tendency for liquid crystal displays to replace cathode ray tubes in response to demands for thinner and smaller display devices. In a liquid crystal display, the liquid crystal unit itself does not have a function to emit light, so in general, V, a so-called knock light device is used that visually illuminates the display by illuminating the liquid crystal unit.
[0003] このバックライト装置の方式としては、 1)光を散乱させる機能を持つ「拡散板」を光 源と液晶ユニットの間に挟んだ、いわゆる直下式と、 2)光源を導光板のエッジに取り 付け、導光板背部の反射板を用いて面方向に光を出すエッジライト方式の 2種類が 通常用いられている。現在はエッジライト方式が主流となっている。特に、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なバッ クライト装置の開発が強く望まれている。  [0003] As a method of this backlight device, 1) a so-called direct type in which a “diffuser plate” having a function of scattering light is sandwiched between a light source and a liquid crystal unit, and 2) an edge of a light guide plate Two types of edge light systems are usually used, which use a reflector behind the light guide plate to emit light in the surface direction. At present, the edge light system is the mainstream. In particular, in recent years, development has continued under the concept of brighter, larger and thinner products, which are increasingly required to increase the brightness, size and thickness of display devices. In particular, there is a strong demand for the development of a backlight device with high brightness using the edge light method.
[0004] このため、バックライト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 くなつている。  [0004] For this reason, for the light guide plate used in the backlight device, there is an extremely strong demand for a light guide plate that efficiently emits incident light incident from a light source lamp disposed on the side surface to the output surface. It is summer.
[0005] このような要求に対して、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、特公昭 39— 1194号公報では導光板の中に 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が示され、特開平 4 — 145485号公報では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が工程が煩雑で ある。 [0005] In response to such demands, a plurality of technical disclosures have been made so far regarding the method of increasing the brightness using a light guide plate. For example, Japanese Patent Publication No. 39-1194 discloses a light guide plate. JP-A-4-145485 discloses a method for obtaining a uniform light emitting surface by dispersing and mixing light diffusing particles. By using a light-scattering plastic material including fine particles having different refractive indexes as a light guide. Although a method for increasing the brightness is disclosed, the process is complicated.
[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] また導光板用の榭脂押出板は、板の表面に傷が付力ないように表面保護フィルム を表裏に貼付した後、所定の幅と長さにするために一般的には鋸で切断されるので 、切粉が表面保護フィルムに付着しやすい。生産された榭脂押出板はパレット等の 上に積載して保管および輸送される。その結果、表面保護フィルムに付着した切粉 は積み重なった板の重みで押し付けられ、板の表面に凹みを生じたり、著しい場合 には表面保護フィルムを破って板の表面に押し傷を生じたりする原因となる。特に海 外に輸出される榭脂押出板では運搬する船の揺れによって板の切粉が表面保護フ イルムを傷つけやすく、さらに板の表面に凹みや傷を生じやす 、。  [0007] In addition, a resin extruded plate for a light guide plate is generally a saw blade in order to have a predetermined width and length after a surface protective film is attached to the front and back so that the surface of the plate is not scratched. Because it is cut with, it is easy for the chips to adhere to the surface protection film. The produced resin extrusion board is loaded on a pallet and stored and transported. As a result, the chips adhering to the surface protection film are pressed by the weight of the stacked plates, causing dents on the surface of the plates, and in severe cases, breaking the surface protection film and causing scratches on the surface of the plates. Cause. In particular, in the case of a resin extruded board exported overseas, the chips on the board are likely to damage the surface protection film due to the shaking of the ship being transported, and the surface of the board tends to be dented or damaged.
[0008] 導光板の表面に切粉による凹みや押し傷が生じると、光源ランプ力 入射した光が 表面の凹みや押し傷の箇所で散乱されていわゆる輝点となり、輝度を低下させる。さ らに凹みや傷が多いと、液晶画面上で見た場合に不具合となる。  [0008] When dents or dents due to chips occur on the surface of the light guide plate, the light incident on the light source lamp force is scattered at the dents or dents on the surface to form so-called bright spots, which lowers the luminance. Furthermore, if there are many dents and scratches, it will be a malfunction when viewed on the LCD screen.
[0009] そもそも切粉が生じないような榭脂押出板の切断方法としては、 1)刃を板の片面ま たは両面力 押し付けて断裁するシヤー切断機、 2)レーザー光線で切断する装置、 3)ウォータージェットで切断する装置などが挙げられる。しかし、これらはいずれも装 置が大掛力りで高価であるば力りでなぐ 1)シヤー切断機は刃が鈍りやすぐ刃の交 換によるランニングコストが大き 、、 2)レーザー切断機は特に厚板の場合に切断面が きれいにならず、溶融した榭脂ミストが板に付着しやぐ反射ミラーの交換のためのラ ンユングコストが大き 、、 3)ウォータージェット切断機は切断面がきれいにならな 、、 などの問題がある。  [0009] In the first place, the method of cutting a resin extruded plate that does not generate chips is as follows: 1) Shear cutting machine that cuts the blade by pressing one side or both sides of the plate, 2) A device that cuts with a laser beam, 3 ) A device that cuts with a water jet. However, all of these devices require a large force if the equipment is large and expensive. 1) Shear cutting machines have a large running cost due to blunting of the blades and immediate replacement of the blades. 2) Laser cutting machines Especially in the case of thick plates, the cutting surface is not clean, and the running cost for replacing the reflecting mirror where molten resin mist adheres to the plate is large. There are problems such as not getting clean.
[0010] 榭脂板を鋸で切断する方法は最も安定生産に適するが、これまでは生じた切粉を 厳密に除去する方法が無力ゝつた。榭脂板を切断後に表面保護フィルムに付着した切 粉をノズル力も圧縮空気で吹き飛ばしても、細かい 0. 1mm2くらいの切粉を厳密に 除去することは [0010] The method of cutting the resin board with a saw is most suitable for stable production, but until now, a method of strictly removing the generated chips has been ineffective. Cutting that adheres to the surface protection film after cutting the resin board Even if the powder is blown away with the nozzle force or compressed air, it is not possible to strictly remove fine chips of about 0.1 mm 2
困難であるば力りでなぐ一旦吹き飛ばした切粉が表面保護フィルムに再付着するこ ともある。板の表裏に吸引ノズルを設けて除去する場合も、細かい切粉を十分に吸い 上げることは困難で、あまりに強く吸引しすぎると板そのものが吸いつけられてしまつ て安定生産を阻害することになる。  If it is difficult, the chips once blown off by force may reattach to the surface protection film. Even when a suction nozzle is installed on the front and back of the board to remove it, it is difficult to suck up fine chips sufficiently.If the suction is too strong, the board itself will be sucked, which will impede stable production. Become.
[0011] また、たとえ切粉が付着しても板の表面に凹みや傷を生じな 、ように保護フィルム の厚みを例えば 90ミクロン以上に厚くする方法もあるが、完全な防止は困難である。  [0011] Although there is a method of increasing the thickness of the protective film to, for example, 90 microns or more so that the surface of the plate does not become dented or scratched even if chips adhere, it is difficult to completely prevent it. .
[0012] 特許文献 1 :特公昭 39— 1194号公報  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
[0013] 本発明の目的は、液晶ディスプレイ向けの高輝度なエッジライト方式バックライト装 置の導光板として好適な、切粉付着の無い榭脂押出板を提供することにある。 [0013] An object of the present invention is to provide a resin-extruded plate suitable for a light guide plate of a high-luminance edge light type backlight device for a liquid crystal display and having no chip adhesion.
課題を解決するための手段  Means for solving the problem
[0014] 本発明者等は、前記課題を解決するために鋭意検討した結果、板の表面保護フィ ルム上の切粉を厳密に除去することによって、ノ ックライト装置の高輝度化を達成しう ることを見出し、本発明を完成させるに至った。 [0014] As a result of intensive investigations to solve the above-mentioned problems, the inventors of the present invention achieve high brightness of the knocklight device by strictly removing the chips on the surface protective film of the plate. As a result, the present invention has been completed.
[0015] すなわち、本発明は板厚みが 2〜15mmの板の表裏に表面保護フィルムが貼られThat is, in the present invention, a surface protective film is applied to the front and back of a plate having a plate thickness of 2 to 15 mm.
、このフィルム上に 0. 1mm2以上の大きさの切粉が無ぐさらに板表面に 0. 1mm2以 上の大きさの凹みおよび Zまたは押し傷が無いことを特徴とする榭脂押出板および その製造方法に関する。 ,榭脂extrusion plate, characterized in that there is no 0. 1 mm 2 or more the size of the chips is the size of the 0. 1 mm 2 or more further plate surface Mugu depressions and Z or push scratches on the film And a manufacturing method thereof.
発明の効果  The invention's effect
[0016] 本発明の榭脂押出板は切粉付着に由来する輝点が無ぐ光源ランプ力 入光した 光の発光効率を最大限に向上させることができる。  [0016] The resin extruded plate of the present invention can maximize the luminous efficiency of the light incident upon the light source lamp force with no bright spots derived from chip adhesion.
図面の簡単な説明  Brief Description of Drawings
[0017] [図 1]本発明における切粉吸引回転ブラシの一例を示したものである。 [図 2]本発明における厚み測定点を示したものである。 [0017] Fig. 1 shows an example of a chip suction rotary brush according to the present invention. FIG. 2 shows thickness measurement points in the present invention.
[図 3]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点評価方法の 一例を示したものである。  FIG. 3 shows an example of a bright spot evaluation method in an edge light type liquid crystal light source device using the light guide plate of the present invention.
[図 4]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. 4 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.
[図 5]本発明における榭脂押出板の製造設備の一例を示したものである。  FIG. 5 shows an example of a production facility for a resin extruded plate according to the present invention.
発明を実施するための最良の形態  BEST MODE FOR CARRYING OUT THE INVENTION
[0018] 本発明について、以下具体的に説明する。 [0018] The present invention will be specifically described below.
[0019] 本発明の榭脂押出板は、原料榭脂を溶融押出成形し、板の形状にすることによつ て製造しうる。原料榭脂としては、メタクリル樹脂(PMMA)、ポリスチレン (PS)、スチ レン Zメチルメタタリレート榭脂(MS)、アクリロニトリル Zスチレン榭脂(SAN)、ポリ力 ーボネート (PC)、非晶質ポリエステル、脂環式ポリオレフイン (三井石油化学の APO 、 日本ゼオンの ZEONEXと ZEONOR、 JSRの ARTONなど)などの透明で溶融成形が 可能な榭脂であれば、いずれも使用できる。また原料榭脂を単独で用いても、輝度を 低下させない範囲で光拡散剤、蛍光増白剤、紫外線吸収剤、酸化防止剤、可塑剤、 離型剤、染料、顔料などの添加剤と混合して使用しても良い。板は単層で押出して 製造しても良いし、共押出法やラミネート法によって二層以上に積層しても差し支え ない。  [0019] The resin-extruded plate of the present invention can be produced by melt-extruding a raw material resin to form a plate. Raw material resin includes methacrylic resin (PMMA), polystyrene (PS), styrene Z-methylmethalate resin (MS), acrylonitrile Z styrene resin (SAN), polycarbonate (PC), amorphous polyester Any alicyclic polyolefin (such as Mitsui Petrochemical's APO, Nippon Zeon's ZEONEX and ZEONOR, JSR's ARTON, etc.) can be used as long as it is transparent and melt-moldable. In addition, even if the raw material is used alone, it is mixed with additives such as light diffusing agents, fluorescent brighteners, ultraviolet absorbers, antioxidants, plasticizers, mold release agents, dyes, pigments, etc., as long as the brightness is not lowered. May be used. The plate may be produced by extruding as a single layer, or may be laminated into two or more layers by a coextrusion method or a laminating method.
[0020] 原料榭脂の中でも、メタタリル榭脂、ポリカーボネート、または脂環式ポリオレフイン が透明性の点で導光板用原料として好適であり、中でもメタクリル榭脂は無色透明性 、耐光性、成形加工性、機械強度、表面硬度などの特性から、特に好ましく用いられ る。  [0020] Among the raw material resin, methallyl resin, polycarbonate, or alicyclic polyolefin is suitable as a raw material for the light guide plate in terms of transparency. Among them, methacrylic resin is colorless and transparent, light resistance, molding processability In view of properties such as mechanical strength and surface hardness, it is particularly preferably used.
[0021] 本発明で特に好適に用いることのできるメタクリル樹脂は、例えば、メタクリル酸メチ ルおよび Zまた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 30重量%未満とを共重合することによって得る事ができる。共重合性を有す る単量体としては、メタクリル酸プロピル、メタクリル酸ブチル、メタクリル酸シクロへキ シル、メタクリル酸 2—ェチルへキシル、メタクリル酸トリシクロデシル、メタクリル酸フエ -ル、メタクリル酸べンジ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、アクリル酸プロピル、アクリル酸ブチル、アクリル酸シクロへキシル、アタリ ル酸 2—ェチルへキシル、アクリル酸トリシクロデシル、アクリル酸フエ-ル、アクリル 酸べンジルなど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、 無水マレイン酸、マレイミド等があげられる力 これらに限定されるものではない。また 、これらの単量体は単独で使用しても、二種類以上を混合して使用しても良い。 [0021] The methacrylic resin that can be used particularly preferably in the present invention is, for example, 70% by weight or more of methyl methacrylate and Z or ethyl methacrylate, and less than 30% by weight of monomers having copolymerizability with these. Can be obtained by copolymerization. Examples of the copolymerizable monomer include propyl methacrylate, butyl methacrylate, cyclohexyl methacrylate, 2-ethylhexyl methacrylate, tricyclodecyl methacrylate, phenol, methacrylate, and methacrylic acid. Methacrylic acid esters such as benzyl, methyl acrylate, acrylic Acrylate esters such as ethyl acid, propyl acrylate, butyl acrylate, cyclohexyl acrylate, 2-ethylhexyl acrylate, tricyclodecyl acrylate, acrylic acid phenyl, benzyl acrylate, methacrylic acid Powers including unsaturated acids such as acid and acrylic acid, maleic anhydride, maleimide and the like are not limited to these. These monomers may be used alone or in combination of two or more.
[0022] 本発明に係る榭脂押出板の原料として用いられる榭脂は、懸濁重合法、乳化重合 法、キャスト重合法、連続塊状重合法、連続溶液重合法などのいずれの重合方法で 得られたものも使用しうる。特に懸濁重合法および連続溶液重合法を用いて製造さ れた榭脂、特にメタタリル榭脂は挟雑物も少なぐ導光板の原料榭脂として好ましい。  [0022] The resin used as the raw material for the resin extruded board according to the present invention can be obtained by any polymerization method such as suspension polymerization, emulsion polymerization, cast polymerization, continuous bulk polymerization, and continuous solution polymerization. Can also be used. In particular, a resin manufactured using a suspension polymerization method and a continuous solution polymerization method, particularly a methallyl resin, is preferable as a raw material resin for a light guide plate with less interstitial material.
[0023] 原材料の一例としてのメタクリル樹脂の懸濁重合法について説明する。まずメタタリ ル酸メチルおよび Zまたはメタクリル酸ェチルと他の共重合可能な単量体とからなる 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。  [0023] A suspension polymerization method of a methacrylic resin as an example of a raw material will be described. First, a polymerization initiator and a chain transfer agent are uniformly dissolved in a monomer mixture composed of methyl metatalate and Z or ethyl methacrylate and another copolymerizable 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. Can be obtained.
[0024] 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等が挙げられる。例えば、ァゾビスイソプチ口-トリル、 2, 2 ,一ァゾビス(2, 4 ジメチルバレロニトリル)、ジメチル一 2, 2'—ァゾビスイソブチレ ート、 t ブチルパーォキシピバレート、 t ブチルパーォキシ 2—ェチノレへキサエー ト、タミルパーォキシ 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 ルパーオキサイド等を挙げることが出来る。これらの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。  [0024] Examples of the polymerization initiator used in suspension polymerization include radical polymerization initiators known for polymerization of vinyl monomers. For example, azobisisobutyl-tolyl, 2,2,1azobis (2,4 dimethylvaleronitrile), dimethyl-1,2,2'-azobisisobutyrate, t-butyl peroxypivalate, t-butyl peroxy 2- Examples include ethinorehexaate, tamperoxy 2-ethyl hexanoate, benzoyl peroxide, lauryl peroxide, and the like. The amount of these polymerization initiators used is preferably in the range of usually 0.01 to 2.0 parts by weight per 100 parts by weight of the monomer or monomer mixture.
[0025] 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、 t—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。 [0026] 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。 [0025] The chain transfer agent used in the suspension polymerization may be a known one used for the polymerization of methyl methacrylate. Examples thereof include t-butyl mercaptan, n-butyl mercaptan, n-octyl mercaptan, t-dodecyl mercaptan and the like. 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. [0026] The dispersion stabilizer used in the suspension polymerization is not particularly limited, but is a poorly water-soluble inorganic compound such as calcium phosphate, calcium carbonate, aluminum hydroxide or the like, polybutyl alcohol, polyethylene oxide, cellulose. Nonionic polymer compounds such as derivatives, polyacrylic acid and its salts, polymethacrylic acid and its salts, copolymer of methacrylic acid ester and methacrylic acid and its salts, etc. I can do it. 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.
[0027] 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 100〜300重量部の範囲が好まし!/、。  [0027] Examples of water used in suspension polymerization include pure water, ion-exchanged water, and deionized water. The amount of water used is not particularly limited, but is preferably in the range of 100 to 300 parts by weight per 100 parts by weight of the monomer or monomer mixture! /.
[0028] 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にする。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。  [0028] The polymerization temperature of the suspension polymerization is not particularly limited, but is about 60 to 120 ° C and a temperature 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.
[0029] さらに必要に応じて光拡散剤、紫外線吸収剤、蛍光増白剤、酸化防止剤、可塑剤 、離型剤、染料、顔料等を懸濁させ重合させても良い。  [0029] Further, if necessary, a light diffusing agent, an ultraviolet absorber, a fluorescent whitening agent, an antioxidant, a plasticizer, a release agent, a dye, a pigment, and the like 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、乾燥することにより球状榭脂 重合体 (例えば、球状メタタリル榭脂重合体)を得ることができる。  After completion of the suspension polymerization, a spherical resin can be obtained (for example, a spherical methallyl resin) by washing, dehydrating and drying by a known method.
[0030] 本発明に係る榭脂押出板の原料として用いられる球状樹脂の平均粒子径は 0. 2 〜0. 5mmであり、好ましくは 0. 25〜0. 39mmである。 0. 2mm未満では良好な板 厚精度が得られず、また 0. 5mmを超えた平均粒子径を有する重合体を安定して製 造することは困難である。  [0030] The average particle size of the spherical resin used as a raw material for the resin extruded plate according to the present invention is 0.2 to 0.5 mm, and preferably 0.25 to 0.39 mm. If it is less than 0.2 mm, good plate thickness accuracy cannot be obtained, and it is difficult to stably produce a polymer having an average particle diameter exceeding 0.5 mm.
[0031] 本発明で榭脂押出板の原料として用いられる榭脂は、懸濁重合法による球状榭脂 のほか、球状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 10〜60トルで押出しダイスよりストランド状に押出し、水冷し、ストランドカツタ 一で切断し得られた円柱状 (ペレット状)の榭脂や、公知の連続溶液重合法、連続塊 状重合法により得られる溶融状態の榭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円柱状 (ペレット状)榭脂を使用しう る。連続溶液重合法、連続塊状重合法の例としては以下の方法が挙げられる。連続 溶液重合法における溶媒としては、蒸留塔ボトム及び蒸留塔内部で原料樹脂の単量 体 (例えば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おり、具体的には、トルエン、キシ レン、ェチルベンゼン、ジェチルベ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、酢酸プチル、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ィ匕合物が挙げられる。特にアルキ ルベンゼン、さらにその中でトルエン、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好ましくは 30重量 %以下、更に好ましくは 25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。 [0031] The resin used as a raw material for the resin extruded plate in the present invention is a spherical resin obtained by suspension polymerization, and a spherical resin is supplied to an extruder equipped with a vent at a temperature of 220 to 260 ° C. Vent vacuum pressure of 10-60 torr. Extruded into strands from extrusion dies, cooled with water, cut into strand cutters (pellet-shaped), and known continuous solution polymerization method, continuous mass Use a cylindrical (pellet-shaped) resin obtained by extruding a molten resin polymer obtained by a state polymerization method into a strand from an extrusion die, water-cooling, and cutting with a strand cutter. The Examples of the continuous solution polymerization method and the continuous bulk polymerization method include the following methods. As a solvent in the continuous solution polymerization method, a monomer of a raw material resin (for example, a monomer capable of copolymerizing with a methyl methacrylate monomer, a methyl methacrylate monomer, and a methyl methacrylate at the bottom of the distillation column and inside the distillation column). More specifically, aromatic compounds such as toluene, xylene, ethylbenzene, and jetylbenzene, aliphatic compounds such as octane and decane, alicyclic compounds such as decalin, acetic acid, etc. Examples include esters such as butyl and pentyl acetate, and halogen compounds such as 1, 1, 2, 2-tetrachloroethane. In particular, alkylbenzene, and among them, toluene, xylene and ethylbenzene are preferable because they have appropriate boiling points, have less degassing load and do not adversely affect polymerization. The amount of the solvent varies depending on the boiling point of the solvent. The amount of the solvent is preferably 30% by weight or less, more preferably 25% by weight or less based on the weight of the total mixture at the time of polymerization. If no solvent is used during polymerization, bulk polymerization occurs.
[0032] 連続溶液重合法、連続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重合開始剤できる。例えば、ジ— 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 - 2, 5 ジ(t—ブチルパーォキシ)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、ジー tー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、ラウリルパーォキシド、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 ジメチルー 4ーメトキシバレロニト リル、 2—シァノー 2, 2—プロピルァゾホルムァシド、 2, 2'—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。  [0032] The polymerization initiator used in the continuous solution polymerization method and the continuous bulk polymerization method can be a polymerization initiator that decomposes actively at the polymerization temperature to generate radicals. For example, di-t-butyl peroxide, dicumyl peroxide, methyl ethyl ketone peroxide, di-t-butyl perphthalate, di-t-butyl perbenzoate, t-butyl peracetate, 2,5-dimethyl-2,5-di (t —Butylperoxy) hexane, 1,1bis (t-butylperoxy) (3,3,5 trimethyl) cyclohexane, 1,1-bis (t-butylperoxy) cyclohexane, di-tamilperoxide, Benzyl peroxide, cumene hydride peroxyside, lauryl peroxide, azobisisobutanol diacetate, 1,1, -azobiscyclohexanecarbonitryl, 2 phenylazole 2,4 dimethyl-4-methoxyvaleronitol, List 2-cyanose, 2,2-propylazoformaside, 2,2'-azobisisobutyryl-tolyl, etc. Can. 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.
[0033] 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。 [0033] Furthermore, 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.
[0034] 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%未満では、揮発成 分による脱揮工程の負荷が大きぐ例えば予備加熱器の伝熱面積の制約力ゝら脱揮 不十分になる場合があり好ましくない。一方、 70%を越えると、例えば、重合反応機 力も予備加熱器間での配管圧力損失が大きくなつて、重合液の輸送が困難となり好 ましくない。重合温度が 120°C未満では重合速度が遅すぎて実用的でなぐまた 16 0°Cを超えると重合速度が速すぎて、重合転化率の調整が困難となる。また、耐熱分 解性が低下し好ましくない。 [0034] The polymerization reactor uses a device that is uniformly stirred by a stirring blade such as a double helical ribbon or a 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. If the polymerization conversion rate is less than 40%, the load of the devolatilization process due to the volatile component is large. For example, the devolatilization may become insufficient due to the restriction of the heat transfer area of the preheater. On the other hand, if it exceeds 70%, for example, the polymerization reaction power is not preferable because the piping pressure loss between the preheaters becomes large and the transport of the polymerization liquid becomes difficult. If the polymerization temperature is less than 120 ° C, the polymerization rate is too slow to be practical, and if it exceeds 160 ° C, the polymerization rate is too high and it is difficult to adjust the polymerization conversion. Further, the heat degradability is lowered, which is not preferable.
[0035] 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 200 〜250°C、 20〜: LOOトルの温度、真空下の脱揮タンクにフィードして重合物を取り出 す。 [0035] 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, etc. are used. Preferably, the polymerization liquid is heated 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, 20 to: LOO Torr temperature, under vacuum Feed the devolatilization tank to remove 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。  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.
[0036] さらに必要に応じて、ダイスよりストランド状に押出す前に、押出機のサイド部よりフ イードポンプを用いて、光拡散剤、紫外線吸収剤、蛍光増白剤、酸化防止剤、可塑 剤、離型剤、染料、顔料等を添加してもよい。  [0036] Further, if necessary, before extruding into a strand from a die, using a feed pump from the side part of the extruder, a light diffusing agent, an ultraviolet absorber, a fluorescent whitening agent, an antioxidant, a plasticizer , Mold release agents, dyes, pigments and the like may be added.
[0037] 本発明の榭脂押出板は溶融押出成形法により製造することが出来る。例えば、原 料榭脂を押出機内で溶融して Tダイカゝら押出し、温度調節された 3、 4ないし 5本のポ リシンダロールの間を順次通して板状 (好ましくは平板状)に成形し、その成形板をガ イドロールの上を通して引き取りロールで引きながら冷却、固化させ、幅方向と流れ 方向を所定の長さに切断することによって枚葉の製品として榭脂押出板を得ることが できる。このときポリシングロールの隙間と引き取り速度を調節することによって所望の 板厚みの榭脂押出板を製造しうる力 一般に導光板用としては 2〜15mmの板厚み の榭脂押出板が使われる。 [0037] The resin extruded plate of the present invention can be produced by a melt extrusion molding method. For example, raw resin is melted in an extruder, extruded from T-Dieka, and passed through three, four to five temperature controlled rolls, and formed into a plate shape (preferably a flat plate shape). The molded plate is cooled and solidified while being drawn with a take-up roll through a guide roll, and a resin extruded plate can be obtained as a single-wafer product by cutting the width direction and the flow direction into predetermined lengths. it can. At this time, the force capable of producing a resin extruded plate having a desired thickness by adjusting the gap between the polishing rolls and the take-off speed Generally, a resin extruded plate having a thickness of 2 to 15 mm is used for the light guide plate.
[0038] 本発明の榭脂押出板は、表面保護フィルムの表面に 0. 1mm2以上の大きさの切粉 が無いことが、導光板として最も重要な特性である。切粉が付着していると、榭脂板を 積載し、さらには輸送する際に重ねられた板の重みで切粉が表面保護フィルムに押 し付けられ、榭脂板の表面に凹みを生じたり、フィルムを破って押し傷を生じたりする [0038]榭脂pushing plate of the present invention, no metal chips 0. 1 mm 2 or more in size to the surface of the surface protective film is the most important property as the light guide plate. If the chips are attached, the resin board is loaded, and further, the chips are pressed against the surface protection film by the weight of the stacked boards when transporting, creating a dent on the surface of the resin board. Or break the film and cause scratches
[0039] 表面保護フィルムに付着した切粉を厳密に除去するために、本発明者らは鋸で榭 脂押出板を切断後、回転ブラシで表面保護フィルムをブラッシングしながら切粉を吸 引、除去することが極めて効果的であることを見出した。 [0039] In order to strictly remove the chips adhering to the surface protective film, the present inventors cut the resin extrusion plate with a saw, and then suck the chips while brushing the surface protective film with a rotating brush. We have found that removal is extremely effective.
[0040] 本発明では榭脂押出板の表面保護フィルムに回転するブラシを接触させるが、ブラ シのフィラメントの材質としては、適度な弾性、柔軟性および対磨耗性を有し、表面保 護フィルムを傷つけたり、榭脂板からめくりあがらせたりしないものであれば、特に限 定しない。ポリプロピレンやナイロン等の合成繊維のほか、植物または動物由来の天 然繊維も用いることができる。静電気の発生を防ぐためには導電性の合成繊維を用 いるのが好ましい。回転ブラシは板の全幅に渡って接触させることが重要である。回 転速度に特に制限は無いが、一般的には 100〜1000rpmの範囲が好ましい。吸引 装置は回転ブラシを内臓し、板表面をブラッシングして切粉を落とした直後に吸引し てしまうことが極めて重要である。回転ブラシと吸引装置を別々に設置した場合は、 本発明の効果は十分には得られない。吸引力は 5kPa以上であれば、通常の切粉を 除去するには十分である。(本発明の図 1参照。 Aは回転ブラシ、 Bは吸引装置カバ 一、 Cは榭脂押出板、 Dは吸引ダクトを示し、 Cからの矢印は、押出方向を示す。 ) また表面保護フィルムに付着した切粉を除去するためには、切断後の板を上下 2本 の粘着ロールの間に通し、表面保護フィルムに付着した切粉を粘着、除去することも 極めて効果的であることを見出した。この場合の粘着ロールは、ポリウレタンや合成ゴ ム等の弾力性がある素材の表面にエチレン Zビニルアルコール等の粘着性物質を 混練あるいは塗布して切粉の粘着、除去を可能にしたものであれば、特に制限無く 使用しうる。また表面保護フィルムに直接接触して切粉を粘着、除去するためのロー ル 1に対して、より粘着力の強いロールを 2接触させることによって、ロール 1に付着し た切粉をロール 2へ移し、ロール 1の表面が清浄な状態に保たれる様、工夫すること ちでさる。 [0040] In the present invention, the rotating brush is brought into contact with the surface protective film of the resin extruded plate. The material of the brush filament has moderate elasticity, flexibility and wear resistance, and the surface protective film. There is no particular limitation as long as it does not hurt or turn off the resin board. In addition to synthetic fibers such as polypropylene and nylon, natural fibers derived from plants or animals can also be used. In order to prevent the generation of static electricity, it is preferable to use conductive synthetic fibers. It is important that the rotating brush is in contact over the entire width of the board. There is no particular limitation on the rotation speed, but generally it is preferably in the range of 100 to 1000 rpm. It is extremely important that the suction device incorporates a rotating brush and sucks immediately after the surface of the plate is brushed to remove chips. When the rotating brush and the suction device are installed separately, the effect of the present invention cannot be obtained sufficiently. A suction force of 5 kPa or more is sufficient to remove normal chips. (See Fig. 1 of the present invention. A is a rotating brush, B is a suction device cover, C is a resin extrusion plate, D is a suction duct, and an arrow from C indicates an extrusion direction.) Also, a surface protective film In order to remove the chips adhering to the surface, it is extremely effective to pass the cut plate between the two upper and lower adhesive rolls to adhere and remove the chips adhering to the surface protective film. I found it. In this case, the adhesive roll can be used to stick and remove chips by kneading or applying an adhesive material such as ethylene Z vinyl alcohol on the surface of elastic materials such as polyurethane and synthetic rubber. If there is no limit Can be used. In addition, the roll 1 for directly adhering to and removing the chips by directly contacting the surface protective film is brought into contact with the roll 1 with 2 more strong adhesive rolls. Move and devise so that the surface of roll 1 is kept clean.
[0041] [実施例] [0041] [Example]
本発明の実施例に基づいて更に具体的に説明する。先ず、本実施例に係る榭脂 押出板についての各測定法を以下に示す。  A more specific description will be given based on examples of the present invention. First, each measuring method about the resin extruded board which concerns on a present Example is shown below.
[0042] (榭脂押出板の厚み測定) [0042] (Measurement of thickness of extruded resin plate)
図 2に示した幅 1000mmの榭脂押出板 1において、幅方向に板厚み測定点 2とし て 5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. Olmmまで 厚みを測定し平均した。榭脂押出板 1の押出方向(図 1の矢印方向)の厚みは板の 両端を長さ 1000mmにわたつて 50mm間隔で板厚み測定点 3として同様に測定し た。  In the 1000 mm wide resin extruded board 1 shown in Fig. 2, the thickness was measured up to 0. Olmm using the outer micrometer (MDC-25M manufactured by Mitutoyo Corporation) as the thickness measurement point 2 in the width direction. Averaged. The thickness of the extruded resin plate 1 in the extrusion direction (in the direction of the arrow in FIG. 1) was measured in the same manner as the plate thickness measurement point 3 at intervals of 50 mm over the length of 1000 mm at both ends of the plate.
[0043] (導光板の輝点の測定方法)  [0043] (Measurement method of bright spot of light guide plate)
図 3に示した光源装置に準じ、ランプハウス Bの中の光源 Aとして 3mm φの冷陰極 管 (ハリソン電気製)を導光板 Cの短辺 (長さ 150mm)側の片面に設置し、光反射シ ート Dとしてレイホワイト 75 (きもと製)を用い、冷陰極管には直流電圧安定装置より 12 Vの電圧をかけて目視で観察し、 0. 1mm2以上の輝点の数を観察する。サンプルを 10枚測定して平均値を出す。 In accordance with the light source device shown in Fig. 3, a cold cathode tube (made by Harrison Electric) with a diameter of 3 mm is installed on one side of the light guide plate C as the light source A in the lamp house B. Ray White 75 (made by Kimoto) is used as the reflective sheet D, and the cold cathode tube is visually observed by applying a voltage of 12 V from a DC voltage stabilizer, and the number of bright spots of 0.1 mm 2 or more is observed. To do. Measure 10 samples and get the average value.
(導光板の輝度、輝度斑の測定方法)  (Measurement method of brightness of light guide plate and brightness spots)
図 3に示した光源装置に準じ、ランプハウス Bの中の光源 Aとして 3mm φの冷陰極 管 (ハリソン電気製)を導光板 Cの長さ 319mm側の両端面に設置し、光反射シート D 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 Eとして 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 2 0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。次いで得られた 361点の測定値力も平均輝度を算出した。  In accordance with the light source device shown in Fig. 3, as the light source A in the lamp house B, a cold-cathode tube of 3mmφ (made by Harrison Electric) is installed on both end faces of the light guide plate C on the length side of 319mm, and the light reflecting sheet D Ray white 75 (manufactured by Kimoto) was used as the light diffusion plate E, and two D121 (manufactured by Gidden) were placed on the light guide plate. The cold cathode tube was charged with a voltage of 12V from a DC voltage stabilizer, and after 20 minutes of lighting, a luminance meter (CA-1000: manufactured by Minolta) placed at a distance of 1 lm from the light emitting surface was used to make the entire light emitting surface 19 X horizontal The luminance of each of the measurement points divided into 19 = 361 was measured. Next, the obtained measurement power of 361 points also calculated the average luminance.
[0044] また、得られた 361点の測定値力も下記 [式 1]により輝度斑の評価指標として均斉 度を算出した。 [0044] In addition, the obtained measured value force of 361 points was also used as an evaluation index for luminance spots by the following [Equation 1]. The degree was calculated.
[0045] [式 1]  [0045] [Formula 1]
均斉度 (%) =最小輝度値 Z最大輝度値 X 100  Uniformity (%) = Minimum luminance value Z Maximum luminance value X 100
(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 0. 5〜0. 15mm7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、各篩上の球状メタクリル樹脂重合体を量り、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。  An electromagnetic shaking sieving meter (electromagnetic vibration AS200 DISIT manufactured by Mitamura Riken Kogyo Co., Ltd.) was used. Sample lOOg is placed on the top sieve of 0.5 ~ 0.15mm 7-stage force, shaken with a shaker for 10 minutes, and the spherical methacrylic resin polymer on each sieve is weighed, and the cumulative residual distribution curve is obtained. Writing, the median diameter was determined and taken as the average particle diameter.
[0046] (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) [0046] (Measuring method of major axis, minor axis, length of cylindrical 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、長さを 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 length of 200 samples were measured to 0.001 mm, and the average value was determined.
(球状メタタリル榭脂重合体 (重合体- A)の製造)  (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 HISO 1139 Condi 3) 1. 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 is cooled to 50 ° C, diluted sulfuric acid is added, washed and dehydrated and dried, and melt flowlay HISO 1139 Condi 3) 1. Spherical methacrylic resin with OgZlO content (polymer A) Got. The average particle diameter of the polymer A was 0.39 mm.
[0047] (円柱状メタクリル榭脂重合体 (重合体 B)の製造) [0047] (Production 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時間で重合し、 重合転化率 53%まで連続的に重合し、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、 30トル、 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(ISO 1139 Condl3) l. OgZlO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 (a)、短径 (b)、長さ (L)は、それぞれ (a) 2. 773mm, (b ) 2. 689mm, (L) 3. 105mm, (b) / (a) 0. 97であった。 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 Add 150ppm of cyclohexane and 300ppm of n-octyl mercaptan and polymerize in a fully mixed polymerization reactor at a polymerization temperature of 155 ° C and a residence time of 2.0 hours. The liquid was continuously removed from the polymerization reactor, then heated to 260 ° C. with a heating plate, and cast and dropped through the space between the heating plates. The devolatilization tank was maintained at 30 torr and 230 ° C, and the polymer was separated from the unreacted monomer and solvent. The polymer is continuously transferred to the extruder in a molten state, and is pushed into a strand from the die through the extruder. It is cooled with water (60 ° C water bath) and cut with a strand cutter to obtain a melt flow rate (ISO 1139 Condl3) l. OgZlO-containing cylindrical methacrylic resin (polymer B) It was. Polymer — B's major axis (a), minor axis (b), and length (L) are (a) 2. 773mm, (b) 2. 689mm, (L) 3. 105mm, (b) / ( a) 0.97.
実施例 1  Example 1
[0048] 重合体 A50重量部と重合体 B50重量部との混合物(計 100重量部)を図 4の 1 )原料ホッパーへ供給し、シリンダー温度がホッパー側力もダイ側へ順に 210、 210、 240、 250、 260、 260。Cに温度調節された 150mm φ単軸押出機 2)で溶融し、リツ プ幅 1250mm、リップ開度 10mmの 3)Tダイから 780kgZ時間の吐出量、榭脂温度 281°Cで押出して水平に配置された 4本の 4)ポリシンダロール(温度は順に 89、 94、 95、 95°C)の間を通し、 5)ガイドロールの上の押出板を 6)引取りロールで引きながら 冷却した。押出ライン周辺の気温は 49°Cであった。ガイドロールの上下には板の表 裏を冷却するための扇風機とエア吹き付け装置を設け、これらを調整することによつ て板の中央と端、表裏の温度分布を制御し、反りの少ない榭脂押出板を製造する。  [0048] A mixture of 50 parts by weight of polymer A and 50 parts by weight of polymer B (total 100 parts by weight) is fed to the raw material hopper in Fig. 4, and the cylinder temperature is 210, 210, 240 in order of the hopper side force to the die side. 250, 260, 260. 150mm φ single screw extruder 2) melted by C, temperature adjusted to 1250mm with lip width of 1250mm, lip opening of 10mm Passed between 4 arranged 4) poly cinder rolls (temperature is 89, 94, 95, 95 ° C in order), 5) cooled while pulling the extruded plate on the guide roll with 6) take-up roll . The temperature around the extrusion line was 49 ° C. A fan and air blowing device are provided above and below the guide roll to cool the front and back of the plate. By adjusting these, the temperature distribution of the center and edges of the plate and the front and back are controlled, and there is little warpage. A fat extrusion board is manufactured.
[0049] 引き取りロール部で板の上下に表面保護用の大王力卩工紙製ポリエチレンマスキン グ (厚み 90ミクロン)を貼付け、 7)トリミング機で板の両端部を切断して幅 1100mmと した。 8)クロスカット機で 1380mmの長さに切断して枚葉とし、上下の 9)切粉吸引回 転ブラシ(500rpm、吸引力 7kPa)を通した後、 10)搬送コンベアで 11)スタッカーへ 送り、 13)パレット上に所定枚数で 12)導光板製品として積載した。なお不良板はパ レットへ積まず、 14)不良払出しへ排出して製品に混入しないようにした。板厚みを 測定したところ、 6. 00±0. 05mmであった。  [0049] A polyethylene masking (90 microns thick) made of Daio Power Paper for surface protection was pasted on the top and bottom of the board at the take-up roll section, and 7) both ends of the board were cut to a width of 1100 mm with a trimming machine. 8) Cut to 1380mm length with a cross-cut machine to make a single sheet, and then pass through the top and bottom 9) chips suction rotating brush (500rpm, suction force 7kPa), 10) feed to conveyor 11) stacker 13) A predetermined number of sheets were loaded on the pallet 12) as light guide plate products. Defective plates were not stacked on the pallet, and 14) discharged to defective dispensing so that they were not mixed into the product. The plate thickness was measured and found to be 6.00 ± 0.05 mm.
[0050] このようにして厚み、幅、および長さが 6 X 1100 X 1380mmの榭脂押出板 Aを得 た。これを観察したところ、表裏に 0. 1mm2以上の切粉の付着は無力つた。 [0050] In this way, a resin extruded plate A having a thickness, width and length of 6 x 1100 x 1380 mm was obtained. When this was observed, chip adhesion of 0.1 mm 2 or more on the front and back sides was helpless.
[0051] この榭脂押出板をパレット上に 100枚積載し、トラックと船舶で静岡県富士巿カも韓 国釜山市まで輸送した。梱包と表面保護フィルムを取り外した後、観察しても 0. 1 mm2以上の凹みや押し傷は見られな力つた。この榭脂押出板をカットして 6 X 150 X 300mmのサイズとし、輝点を測定したところ、検知されな力つた。 [0051] 100 sheets of this resin extrusion board were loaded on a pallet, and Fujioka in Shizuoka Prefecture was also transported to Busan City, South Korea by truck and ship. After removing the packaging and the surface protection film, even when observed, no dents or scratches of 0.1 mm 2 or more were observed. This resin extruded plate was cut to a size of 6 X 150 X 300 mm and measured for a bright spot.
[0052] 次いで輸送後の榭脂押出板 Aから幅 241mm、長さ 319mmのサイズに丸鋸を用 、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、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 SR 931 (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 。輝度を測定した結果、 2900cdであった。これらの結果を表 1に示す。 [0052] Next, use a circular saw with a size of 241mm in width and 319mm in length from the extruded resin board A after transportation. Then, the cut surface of the cut plate is polished with a precision polishing machine (PLA—Beauty: manufactured by Megalotech-Power Co., Ltd.), further puffed and finished to a mirror surface, and then 15 inch size dots Using a printing screen with gradation, using Mattmedium SR 931 (manufactured by Mino Group) as ink, screen printing was performed on one side of the light guide plate to obtain a light guide plate. As a result of measuring the luminance, it was 2900 cd. These results are shown in Table 1.
実施例 2  Example 2
[0053] 切粉吸引回転ブラシを用いず、板を上下 2本の粘着ロールに挟んで、切粉を吸引 除去したほかは、実施例 1と同様にして榭脂押出板 Bを得た。凹みまたは押し傷、切 粉、輝点および輝度の測定結果を表 1に示す。  [0053] A resin extruded plate B was obtained in the same manner as in Example 1 except that the chips were sandwiched between two upper and lower adhesive rolls and the chips were removed by suction without using the chip suction rotating brush. Table 1 shows the measurement results of dents or dents, chips, bright spots and brightness.
[比較例 1]  [Comparative Example 1]
切粉吸引回転ブラシを用いず、板表裏を 7kPaの吸引力で吸引するだけにしたほ かは、実施例 1と同様にして榭脂押出板 Cを得た。凹みまたは押し傷、切粉、輝点お よび輝度の測定結果を表 1に示す。  A resin extruded plate C was obtained in the same manner as in Example 1 except that the chip suction rotary brush was not used and only the front and back sides of the board were sucked with a suction force of 7 kPa. Table 1 shows the measurement results of dents or dents, chips, bright spots and brightness.
[比較例 2]  [Comparative Example 2]
切粉吸引回転ブラシを用いず、板表裏を圧縮空気で吹くだけにしたほかは、実施 例 1と同様にして榭脂押出板 Dを得た。凹みまたは押し傷、切粉、輝点および輝度の 測定結果を表 1に示す。  A resin extruded plate D was obtained in the same manner as in Example 1 except that the chip suction rotating brush was not used and only the front and back of the plate were blown with compressed air. Table 1 shows the measurement results of dents or dents, chips, bright spots and brightness.
[0054] [表 1] [0054] [Table 1]
Figure imgf000015_0001
Figure imgf000015_0001
[0055] (結果の概要) 以上の実施例および比較例で示したように、本発明の切粉吸引回転ブラシや粘着 ロールを用いな 、場合は榭脂板の表面保護フィルムの上に切粉が残り、陸上および 海上輸送後の板の表面には凹みや押し傷が生じ、輝点の発生や輝度低下が見られ るので、ノ ックライトユニット用の導光板としては好ましくない。 [0055] (Summary of results) As shown in the above examples and comparative examples, when the chip suction rotating brush and the adhesive roll of the present invention are not used, chips remain on the surface protective film of the resin board, and after transportation on land and sea. Since the surface of the plate has dents and scratches, and generation of bright spots and a decrease in luminance are observed, it is not preferable as a light guide plate for a knock light unit.
産業上の利用可能性 Industrial applicability
本発明の榭脂押出板は、ノートブック型またはデスクトップ型のパーソナルコンビュ ータ、携帯情報端末、ゲーム機、ワークステーション、画像モニター、あるいはテレビ 等の表示装置としての液晶ディスプレイにおいて、液晶を背面力も照らすバックライト 装置に用いられる導光板として好適に使用できる。  The resin extruded plate of the present invention is used for a liquid crystal display as a display device such as a notebook or desktop personal computer, a portable information terminal, a game machine, a workstation, an image monitor, or a television. It can be suitably used as a light guide plate used in an illuminating backlight device.

Claims

請求の範囲 The scope of the claims
[1] 板に表面保護フィルムが貼られ、当該フィルム上に 0. 1mm2以上の大きさの切粉 が無ぐさらに板表面に 0. 1mm2以上の大きさの凹みおよび Zまたは押し傷が無い 榭脂押出板。 [1] A surface protective film is applied to the board, there is no chip of 0.1 mm 2 or more on the film, and there are dents of 0.1 mm 2 or more and Z or scratches on the surface of the board. No rosin extrusion board.
[2] 原料樹脂がメタクリル樹脂、ポリカーボネート、または脂環式ポリオレフインである、 請求項 1に記載の榭脂押出板。  [2] The resin extruded plate according to claim 1, wherein the raw material resin is a methacrylic resin, a polycarbonate, or an alicyclic polyolefin.
[3] 原料樹脂が球状メタタリル榭脂であり、平均粒子径が 0. 2〜0. 5mmである請求項[3] The raw material resin is spherical metataryl resin, and the average particle size is 0.2 to 0.5 mm.
1に記載の榭脂押出板。 1. The resin extruded board according to 1.
[4] 板厚みが 2〜 15mmである請求項 1に記載の榭脂押出板。 [4] The resin extruded plate according to claim 1, wherein the plate thickness is 2 to 15 mm.
[5] 溶融榭脂を用いて板状に押出成形し、その成形板をガイドロールの上を通して引き 取りロールで引きながら冷却、固化させ、表裏に表面保護フィルムを貼付した後、幅 方向と流れ方向を所定の長さに切断する榭脂押出板の製造方法において、切断後 に回転ブラシで表面保護フィルムをブラッシングしながら切粉を吸引、除去することに よって表面保護フィルム上に切粉が無いようにする榭脂押出板の製造方法。  [5] Extruded into a plate shape using molten resin, cooled and solidified while pulling the formed plate through the take-up roll with a take-up roll, and pasted the surface protection film on the front and back, then the width direction and flow In the method of manufacturing a resin extruded plate that cuts the direction to a predetermined length, there is no swarf on the surface protective film by sucking and removing the chips while brushing the surface protective film with a rotating brush after cutting. A method for producing a resin extruded plate.
[6] 溶融榭脂を用いて板状に押出成形し、その成形板をガイドロールの上を通して引き 取りロールで引きながら冷却、固化させ、表裏に表面保護フィルムを貼付した後、幅 方向と流れ方向を所定の長さに切断する榭脂押出板の製造方法において、切断後 の板を上下 2本の粘着ロールの間に通し、表面保護フィルムに付着した切粉を粘着 、除去することによって表面保護フィルム上に切粉が無いようにする榭脂押出板を製 造する方法。  [6] Extruded into a plate shape using molten resin, cooled and solidified while pulling the formed plate through the take-up roll with the take-up roll, and pasted the surface protection film on the front and back, then the width direction and flow In a method for producing a resin extruded plate that cuts the direction to a predetermined length, the cut plate is passed between two upper and lower adhesive rolls to adhere and remove the chips adhering to the surface protective film. A method of producing a resin-extruded plate that eliminates chips on the protective film.
[7] 温度調節された 3から 5本のポリシングロールの間を順次通して板状に成形するェ 程を含む請求項 5または 6に記載の榭脂押出板の製造方法。  7. The method for producing a resin-extruded plate according to claim 5 or 6, further comprising a step of forming a plate by sequentially passing between 3 to 5 polishing rolls adjusted in temperature.
PCT/JP2005/020819 2004-11-19 2005-11-14 Resin extruded plate for optical use and method for manufacturing same WO2006054510A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2006545003A JPWO2006054510A1 (en) 2004-11-19 2005-11-14 Optical resin extrusion plate and manufacturing method thereof

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2004335909 2004-11-19
JP2004-335909 2004-11-19

Publications (1)

Publication Number Publication Date
WO2006054510A1 true WO2006054510A1 (en) 2006-05-26

Family

ID=36407053

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2005/020819 WO2006054510A1 (en) 2004-11-19 2005-11-14 Resin extruded plate for optical use and method for manufacturing same

Country Status (5)

Country Link
JP (1) JPWO2006054510A1 (en)
KR (1) KR20070074630A (en)
CN (1) CN101060966A (en)
TW (1) TW200630202A (en)
WO (1) WO2006054510A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105922489A (en) * 2016-06-06 2016-09-07 何浩然 Full-automatic plastics rolling moulder capable of precise length control

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW201005324A (en) * 2008-07-16 2010-02-01 Entire Technology Co Ltd Optical film structure and its manufacture method
CN103175098A (en) * 2012-05-17 2013-06-26 杨振安 Light-emitting diode (LED) light guide plate and manufacturing method thereof

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07237186A (en) * 1994-03-01 1995-09-12 Tsutsunaka Plast Ind Co Ltd Chip removing method and chip removing device for long size material
JP2001205210A (en) * 2000-01-24 2001-07-31 Reyoon Kogyo:Kk Mechanism for treating edge of panel material and apparatus for treating edge of panel material using the same
JP2002172707A (en) * 2000-12-07 2002-06-18 Sumitomo Chem Co Ltd Method and apparatus for manufacturing sheet product without foreign adherent
JP2003270447A (en) * 2002-03-15 2003-09-25 Asahi Kasei Corp Light guide body

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07237186A (en) * 1994-03-01 1995-09-12 Tsutsunaka Plast Ind Co Ltd Chip removing method and chip removing device for long size material
JP2001205210A (en) * 2000-01-24 2001-07-31 Reyoon Kogyo:Kk Mechanism for treating edge of panel material and apparatus for treating edge of panel material using the same
JP2002172707A (en) * 2000-12-07 2002-06-18 Sumitomo Chem Co Ltd Method and apparatus for manufacturing sheet product without foreign adherent
JP2003270447A (en) * 2002-03-15 2003-09-25 Asahi Kasei Corp Light guide body

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105922489A (en) * 2016-06-06 2016-09-07 何浩然 Full-automatic plastics rolling moulder capable of precise length control

Also Published As

Publication number Publication date
KR20070074630A (en) 2007-07-12
JPWO2006054510A1 (en) 2008-05-29
CN101060966A (en) 2007-10-24
TW200630202A (en) 2006-09-01

Similar Documents

Publication Publication Date Title
WO2006054509A1 (en) Resin extruded plate for high luminance light guide plate and method for producing the same
TW567344B (en) Light guide and method for producing transparent thermoplastic resin composition for light guide
KR101398507B1 (en) White polyester film for light reflective plate
CN101313175B (en) Light guide plate
TW201222097A (en) Television receiver and surface light source device
JP5326878B2 (en) Lens sheet base film
WO2006054510A1 (en) Resin extruded plate for optical use and method for manufacturing same
TW201111435A (en) Acrylic film for punching, plane light source apparatus, and fabricating method of optical element
TWI314627B (en) Optical waveguide and process for producing the same
KR100889409B1 (en) Resin extruded plate and method for producing the same
JP2009302034A (en) Acrylic sheet or film for thin light guide plate
KR20160137992A (en) Laminated film
KR102590694B1 (en) white reflective film
JP2006106185A (en) Light diffusion multilayer plate
KR100857501B1 (en) Optical methacrylic resin extrusion plate manufacturing method
JP2001195914A (en) Lightguide plate for color monitor of acrylic resin series
CN1809768A (en) Light-reflector and planar light source using same
JP4711967B2 (en) New extruded plate of methacrylic resin and method for producing the same
JP4941762B2 (en) Optical film
JP2006032254A (en) Light guide plate with hole
JP2009151226A (en) Optical sheet, backlight unit and display device
JP2012081646A (en) Optical polyester film

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KM KN KP KR KZ LC LK LR LS LT LU LV LY MA MD MG MK MN MW MX MZ NA NG NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SM SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LT LU LV MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
WWE Wipo information: entry into national phase

Ref document number: 2006545003

Country of ref document: JP

WWE Wipo information: entry into national phase

Ref document number: 200580039245.4

Country of ref document: CN

WWE Wipo information: entry into national phase

Ref document number: 1020077011349

Country of ref document: KR

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 05806320

Country of ref document: EP

Kind code of ref document: A1