JPH01172801A - Light diffusion plate having light transmittability - Google Patents
Light diffusion plate having light transmittabilityInfo
- Publication number
- JPH01172801A JPH01172801A JP62329945A JP32994587A JPH01172801A JP H01172801 A JPH01172801 A JP H01172801A JP 62329945 A JP62329945 A JP 62329945A JP 32994587 A JP32994587 A JP 32994587A JP H01172801 A JPH01172801 A JP H01172801A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- plate
- transparent
- paint
- spherical particles
- Prior art date
- Legal status (The legal status 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 status listed.)
- Granted
Links
- 238000009792 diffusion process Methods 0.000 title abstract description 15
- 239000002245 particle Substances 0.000 claims abstract description 45
- 239000012798 spherical particle Substances 0.000 claims abstract description 37
- 229920005989 resin Polymers 0.000 claims abstract description 36
- 239000011347 resin Substances 0.000 claims abstract description 36
- 238000002834 transmittance Methods 0.000 claims abstract description 35
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 25
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims abstract description 19
- 229920002050 silicone resin Polymers 0.000 claims abstract description 13
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 12
- 239000007787 solid Substances 0.000 claims abstract description 9
- 239000003973 paint Substances 0.000 claims description 55
- 238000000576 coating method Methods 0.000 claims description 36
- 239000011248 coating agent Substances 0.000 claims description 29
- 239000000463 material Substances 0.000 claims description 26
- 125000000962 organic group Chemical group 0.000 claims description 18
- 239000000758 substrate Substances 0.000 claims description 16
- -1 polysiloxane Polymers 0.000 claims description 11
- 239000000178 monomer Substances 0.000 claims description 9
- 238000002156 mixing Methods 0.000 abstract description 11
- 229920000642 polymer Polymers 0.000 abstract description 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract description 4
- 229910052760 oxygen Inorganic materials 0.000 abstract description 4
- 239000001301 oxygen Substances 0.000 abstract description 4
- 230000005540 biological transmission Effects 0.000 abstract description 2
- 230000003247 decreasing effect Effects 0.000 abstract description 2
- 238000000034 method Methods 0.000 description 31
- 239000000113 methacrylic resin Substances 0.000 description 23
- 230000003287 optical effect Effects 0.000 description 16
- 239000002904 solvent Substances 0.000 description 16
- 238000001723 curing Methods 0.000 description 12
- 229920003023 plastic Polymers 0.000 description 11
- 239000003795 chemical substances by application Substances 0.000 description 10
- 238000009826 distribution Methods 0.000 description 9
- 239000004973 liquid crystal related substance Substances 0.000 description 9
- 239000000047 product Substances 0.000 description 8
- 239000011521 glass Substances 0.000 description 7
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical group COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 6
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 6
- 239000010410 layer Substances 0.000 description 6
- 125000005395 methacrylic acid group Chemical group 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 238000012545 processing Methods 0.000 description 6
- 239000011541 reaction mixture Substances 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 5
- 230000002776 aggregation Effects 0.000 description 5
- 238000004062 sedimentation Methods 0.000 description 5
- 229920003002 synthetic resin Polymers 0.000 description 5
- 239000003086 colorant Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 125000000524 functional group Chemical group 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 238000006460 hydrolysis reaction Methods 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 4
- 229920001225 polyester resin Polymers 0.000 description 4
- 239000004645 polyester resin Substances 0.000 description 4
- 239000004926 polymethyl methacrylate Substances 0.000 description 4
- 239000000057 synthetic resin Substances 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 3
- 238000004220 aggregation Methods 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 229920005668 polycarbonate resin Polymers 0.000 description 3
- 239000004431 polycarbonate resin Substances 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
- 229910000077 silane Inorganic materials 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 238000005054 agglomeration Methods 0.000 description 2
- 229920000180 alkyd Polymers 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 2
- SBRXLTRZCJVAPH-UHFFFAOYSA-N ethyl(trimethoxy)silane Chemical compound CC[Si](OC)(OC)OC SBRXLTRZCJVAPH-UHFFFAOYSA-N 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000000691 measurement method Methods 0.000 description 2
- BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 description 2
- 238000007645 offset printing Methods 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000002985 plastic film Substances 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920005749 polyurethane resin Polymers 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- CPUDPFPXCZDNGI-UHFFFAOYSA-N triethoxy(methyl)silane Chemical compound CCO[Si](C)(OCC)OCC CPUDPFPXCZDNGI-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- 239000004923 Acrylic lacquer Substances 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 238000003848 UV Light-Curing Methods 0.000 description 1
- ZCZFEIZSYJAXKS-UHFFFAOYSA-N [3-hydroxy-2,2-bis(hydroxymethyl)propyl] prop-2-enoate Chemical compound OCC(CO)(CO)COC(=O)C=C ZCZFEIZSYJAXKS-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- 238000012644 addition polymerization Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001335 aliphatic alkanes Chemical group 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000008094 contradictory effect Effects 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 210000002858 crystal cell Anatomy 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000001227 electron beam curing Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- JDVIRCVIXCMTPU-UHFFFAOYSA-N ethanamine;trifluoroborane Chemical compound CCN.FB(F)F JDVIRCVIXCMTPU-UHFFFAOYSA-N 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 230000006355 external stress Effects 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000007646 gravure printing Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000003504 photosensitizing agent Substances 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 239000000088 plastic resin Substances 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 238000012643 polycondensation polymerization Methods 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 238000011417 postcuring Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000007142 ring opening reaction Methods 0.000 description 1
- 239000011833 salt mixture Substances 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- KQSJSRIUULBTSE-UHFFFAOYSA-M sodium;3-(3-ethylcyclopentyl)propanoate Chemical compound [Na+].CCC1CCC(CCC([O-])=O)C1 KQSJSRIUULBTSE-UHFFFAOYSA-M 0.000 description 1
- 238000000935 solvent evaporation Methods 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229920006027 ternary co-polymer Polymers 0.000 description 1
- 238000012719 thermal polymerization Methods 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- JCVQKRGIASEUKR-UHFFFAOYSA-N triethoxy(phenyl)silane Chemical compound CCO[Si](OCC)(OCC)C1=CC=CC=C1 JCVQKRGIASEUKR-UHFFFAOYSA-N 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本発明は、光拡散性にすぐれたプラスチック製拡散板に
関するもので、更に詳しくはシリコーン樹脂球状粒子を
透明性樹脂に配合分散せしめた全光線透過率と色温度を
高めた光拡散板及び、前記球状粒子を透明性塗料に混合
分散せしめ透明基板に塗布せしめた光拡散板に関する。[Detailed Description of the Invention] <Industrial Field of Application> The present invention relates to a plastic diffuser plate with excellent light diffusing properties, and more specifically, it relates to a plastic diffuser plate with excellent light diffusing properties. The present invention relates to a light diffusing plate with increased transmittance and color temperature, and a light diffusing plate in which the spherical particles are mixed and dispersed in a transparent paint and coated on a transparent substrate.
〈従来の技術〉
光拡散性プラスチック板としては、従来よりメタクリル
樹脂板、ポリカーボネート樹脂板、ポリ塩化ビニル樹脂
板等の透明性プラスチックシートに無機性或いは有機性
光拡散剤を配合したものが開発され使用されているほか
、ポリエステルフィルム等の薄いフィルムによる光拡散
性フィルムも使用されるようになってきた。<Prior art> As light-diffusing plastic plates, transparent plastic sheets such as methacrylic resin plates, polycarbonate resin plates, and polyvinyl chloride resin plates have been blended with inorganic or organic light-diffusing agents. In addition to this, thin light-diffusing films such as polyester films have also come into use.
これら光拡散性プラスチックシートの用途は、照明用、
グレージング用のほか、看板、後方から投影した文字、
画像等を写しだすりアーブロジェクションスクリーン用
として、或いは各種宣伝広告等のプリントフィルムの明
るさを確保し、光源を拡散せしめるための乳白色の拡散
シートとしても使用されている。更に最近ではワードプ
ロセッサー等のOA機器に採用されている液晶デイスプ
レー、或いは液晶カラーテレビのバックライト光源の拡
散板にも使用されるよう−になってきた。These light-diffusing plastic sheets are used for lighting,
In addition to glazing, signboards, letters projected from the rear,
It is also used as an arbor projection screen for projecting images, or as a milky-white diffusion sheet to ensure the brightness of print films for various advertisements and to diffuse light sources. Furthermore, recently, they have come to be used in liquid crystal displays used in office automation equipment such as word processors, and in diffusers for backlight sources in liquid crystal color televisions.
これら光拡散性プラスチック板の製造には、透明プラス
チック材料に炭酸カルシウム、酸化チタン、硫酸バリウ
ム、タルク、シリカ等の無機系光拡散剤を混合分散せし
め、押出機で板状に押出して板状物とするのが通常の方
法である。又、これら光拡散剤を透明なプラスチック板
の表面に塗布する方法も用いられている。To manufacture these light-diffusing plastic plates, inorganic light-diffusing agents such as calcium carbonate, titanium oxide, barium sulfate, talc, and silica are mixed and dispersed in a transparent plastic material, and the mixture is extruded into a plate shape using an extruder. This is the usual method. Also, a method of applying these light diffusing agents to the surface of a transparent plastic plate is also used.
その他有機系分散剤として屈折率の異なる粉体が、フッ
素樹脂を始めメタクリル樹脂、エボギシ樹脂、ペンゾグ
アカミン、ポリエチレン、ナイロン、フェノール等の樹
脂が透明プラスチックに混合分散せしめて使用されるよ
うになっている。しかしながら、光の高透過率と高拡散
率が厳しく要求される。Other organic dispersants include powders with different refractive indexes, such as fluororesin, methacrylic resin, epoxy resin, penzoguacamine, polyethylene, nylon, and phenol, which are mixed and dispersed in transparent plastics. . However, high light transmittance and high diffusivity are strictly required.
〈発明が解決しようとする問題点〉
特に近年急速に普及してきた液晶デイスプレー(二不可
欠のバックライト用の拡散板のような用途では、これら
従来製品での対応が極めて困難になってきている状況(
二ある。<Problems to be solved by the invention> In particular, it has become extremely difficult to use conventional products for applications such as diffusion plates for backlights, which are essential for LCD displays, which have become rapidly popular in recent years. situation(
There are two.
従来の製品で、光の透過率(全光線透過率)を高めよう
とすると、混合されている光拡散剤の量を低減せざるを
得ない事から拡散率が低下する。When attempting to increase the light transmittance (total light transmittance) of conventional products, the amount of light diffusing agent mixed must be reduced, resulting in a decrease in the diffusivity.
拡散率を高めようとすると光拡散剤の添加量を増量せざ
るを得す、この結果として全光線透過率が低下するとい
うことになる。すなわち、全光線透過率と拡散率とは背
反関係にあるが実情である。In order to increase the diffusivity, it is necessary to increase the amount of light diffusing agent added, and as a result, the total light transmittance decreases. That is, the actual situation is that total light transmittance and diffusivity are in a contradictory relationship.
本発明者は、このような実情を鑑み、全光線透過率を低
減せしめず、拡散率を高める拳を、又最近普及しつつあ
る液晶カラーテレビの拡散板に要求される色温度も、従
来製品よりも更に高めることを又、よりフラットな輝度
分布を実現することなども目的に鋭意研究し本発明に至
った。In view of these circumstances, the inventors of the present invention have developed a technology that increases the diffusion rate without reducing the total light transmittance, and also improves the color temperature required for the diffuser panels of LCD color televisions, which have recently become popular. The present invention was achieved through intensive research aimed at further increasing the luminance distribution and achieving a flatter luminance distribution.
く問題点を解決するための手段〉
本発明は
/ 珪素原子に透明性樹脂又はそのモノマーに対する親
和性を有する有機基が直結したポリシロキサン結合をな
す固体状のシリコーン樹脂からなる数平均粒子径0.3
〜70μの球状粒子が透明性樹脂板中1=該透明性樹脂
に対して/〜!0wt%混合、分散されて存在す゛るこ
とを特徴とする光透過性を有する光拡散板
コ 珪素原子に透明性塗料中の塗膜形成材料又はその七
ツマ−に対する親和性を有する有機基が直結したポリシ
ロキサン結合をなす固体状のシリコーン樹脂からなる数
平均粒子径0.3〜/θμの球状粒子を透明性塗料中に
、該を料中の前記塗膜形成材料又はその七ツマ−に対し
て/〜s o wt*混合、分散せしめ該塗料を透明基
板の少くとも片側に塗布したことを特徴とする光透過性
を有する光拡散板
を提供する。Means for Solving the Problems> The present invention consists of a solid silicone resin having a number average particle diameter of 0, in which a silicon atom is directly connected to a transparent resin or an organic group having an affinity for its monomer, forming a polysiloxane bond. .3
~70μ spherical particles in the transparent resin plate 1=with respect to the transparent resin/~! A light diffusing plate having light transmittance characterized by being mixed and dispersed at 0 wt%. An organic group having an affinity for a coating film-forming material in a transparent paint or its seven molecules is directly bonded to a silicon atom. Spherical particles made of a solid silicone resin forming a polysiloxane bond and having a number average particle diameter of 0.3 to /θμ are added to a transparent paint relative to the coating film-forming material or its constituents in the material. /~s o wt* A light diffusing plate having light transmittance characterized in that the mixed and dispersed paint is coated on at least one side of a transparent substrate.
本発明に用いるシリコーン樹脂としてはケイ素原子に有
機基が直結し、残りの結合が酸素と直結しており、ケイ
素原子と酸素が繰り返すシロキサン結合でポリマーとな
ったものである。こ\で本発明の球状粒子は、常温又は
それ以上の温度で固体状である。さらに好ましくは、後
に述べる透明性樹脂板又は透明基板のプレス延伸等によ
る2次加工の温度下でも固体状を維持し得るものである
。The silicone resin used in the present invention has an organic group directly bonded to a silicon atom, and the remaining bonds are directly bonded to oxygen, and is a polymer formed by repeating siloxane bonds between silicon atoms and oxygen. The spherical particles of the present invention are solid at room temperature or higher. More preferably, it is one that can maintain a solid state even under the temperature of secondary processing such as press stretching of a transparent resin plate or transparent substrate, which will be described later.
さら(:好ましくは、該シロキチン結合が三次元の網状
構造を示す固体状ポリマーである。ケイ素原子に結合す
る有機基の数は、その種類、透明性樹脂(二対する親和
力によっても異るが、好ましくは平均で0.5〜1.3
個、より好ましくは0.7〜7.3個である。Furthermore, it is preferably a solid polymer in which the silochitin bonds exhibit a three-dimensional network structure.The number of organic groups bonded to the silicon atom varies depending on the type thereof and the affinity for the transparent resin ( Preferably 0.5 to 1.3 on average
, more preferably 0.7 to 7.3.
ケイ素原子に結合した有機基で覆われた表面を有するシ
リコーン樹脂の球状粒子は、有機溶剤に良好に分散し溶
剤の粘度を高める効果を示す。本発明で用いられる球状
粒子は溶剤に分散した時の粘度(溶剤がn−へキチン、
球状粒子の混合量がn−へキチンに対し100Wtチ、
常温、B型回転粘度計、40rpmで測定)、200〜
jθQ CpSを示すものが好ましく採用される。更に
望ましくは300〜4t o o cpsの範囲(:あ
る。Spherical particles of silicone resin having a surface covered with organic groups bonded to silicon atoms are well dispersed in organic solvents and have the effect of increasing the viscosity of the solvent. The spherical particles used in the present invention have a viscosity when dispersed in a solvent (the solvent is n-hexitine,
The mixed amount of spherical particles is 100 Wt for n-hexitine,
Measured at room temperature, B-type rotational viscometer, 40 rpm), 200~
Those exhibiting jθQ CpS are preferably employed. More preferably, it is in the range of 300 to 4 t o cps.
第7図に本発明に用いるシリコーン樹脂球状粒子の分子
構造モデルの7例を示す。FIG. 7 shows seven examples of molecular structure models of silicone resin spherical particles used in the present invention.
第1図のモデルは、シロキチン結合が三次元に伸びた網
状構造であり、ケイ素原子に7個の有機基が結合した構
造である。このモデルは本発明の実施態様としては最も
好ましい例である。The model shown in FIG. 1 is a network structure in which xylochitin bonds extend in three dimensions, and has a structure in which seven organic groups are bonded to a silicon atom. This model is the most preferred embodiment of the present invention.
本発明のシリコーン樹脂はガラスのような無機的性質と
有機基による有機的な性質とを合わせ持つ中間的な性質
の物質である。又、第7図に示した如く、球状粒子表面
はケイ素原子に強固に直結した有機基に覆われた構造と
なっているので透明性樹脂又はその重合性モノマーへの
分散性がきわめて良好である。更にはきわめて意外な効
果として光学的特性の著しい改善に帰与することが、本
発明により初めて明らか(ニされた。The silicone resin of the present invention is a substance with intermediate properties having both inorganic properties such as glass and organic properties due to organic groups. In addition, as shown in Figure 7, the surface of the spherical particles has a structure covered with organic groups that are firmly and directly bonded to silicon atoms, so the dispersibility in transparent resins or their polymerizable monomers is extremely good. . Furthermore, it has been revealed for the first time by the present invention that the optical properties are significantly improved as a very unexpected effect.
本発明において用い得る有機基としては例えばメチル基
、エチル基、プロピル基、ブチル基等のアルカン基はも
とより、カルボキシル基、カルボニル基、エステル基、
エーテル基等本発明に用いる透明性樹脂又はそのモノマ
ーに対して親和力を有する有機基を含む。代表的な有機
基としてメチル基があげられる。Examples of organic groups that can be used in the present invention include alkane groups such as methyl, ethyl, propyl, and butyl groups, as well as carboxyl groups, carbonyl groups, ester groups,
It contains an organic group such as an ether group that has an affinity for the transparent resin used in the present invention or its monomer. A typical organic group is a methyl group.
珪素原子に直結した前記有機基が平均で0.5個未満で
あると透明樹脂或いは透明性塗料中の塗膜形成材料への
単分散が困難となる傾向があることもありまたは単分散
しても二次凝集が生じ粒子が肥大化し、光学的に不均一
な拡散板が得られる傾向となることもあり得る。If the number of organic groups directly bonded to silicon atoms is less than 0.5 on average, it may be difficult to monodisperse the organic group into a transparent resin or a coating film-forming material in a transparent paint. There is also a possibility that secondary aggregation occurs and the particles become enlarged, resulting in a tendency to obtain an optically non-uniform diffuser plate.
一方珪素原子に直結した有機基が平均で/、5個を超え
た場合、ポリシロキサン結合の三次元網状構造体の形成
や球状の形成が生じがたくなったり、あるいはまた外部
応力で容易に変形しやすい粒子となったりする傾向が出
ることもある。On the other hand, if the number of organic groups directly bonded to silicon atoms exceeds 5 on average, it becomes difficult to form a three-dimensional network structure of polysiloxane bonds or to form a spherical structure, or it becomes easily deformed by external stress. There may also be a tendency for particles to form easily.
本発明に使用するシリコーン球状粒子を製造するための
原料として例えば官能基3個をもつ加水分解性シランが
用い得られる。加水分解と縮合の工程(:よって次のよ
うな反応機構を経て、第1図のような3次元的網目構造
をとる粒子が形成されると推定されている。For example, a hydrolyzable silane having three functional groups can be used as a raw material for producing the silicone spherical particles used in the present invention. It is presumed that particles with a three-dimensional network structure as shown in Figure 1 are formed through the following reaction mechanism: hydrolysis and condensation steps.
この加水分解と重縮合反応の工程に於いて、使用される
加水分解性シランの官能基および有機基の種類、加水分
解触媒の種類と量(酸、アルカリ)、反応装置の構造、
攪拌条件(二よって粒子の形状、粒径が微妙(二影響さ
れ、これら粒子形成時の影響因子の制御により、所望の
ものを作ることが可能となる。In this hydrolysis and polycondensation reaction process, the types of functional groups and organic groups of the hydrolyzable silane used, the type and amount of the hydrolysis catalyst (acid, alkali), the structure of the reaction equipment,
The shape and size of the particles are delicately affected by the stirring conditions (2), and by controlling these influencing factors during particle formation, it is possible to produce the desired product.
本発明において、球状粒子の形状は不定形でないことが
光学的特性を得るうえで必要である。粒子の形態として
は使用条件、目的によっても異るが、ダ円球形状ないし
真球形状にわたる形態が好ましく、なかでも真球形状又
はこれに近い形状が最も好ましい。In the present invention, it is necessary that the shape of the spherical particles is not amorphous in order to obtain optical properties. Although the shape of the particles varies depending on the conditions of use and purpose, it is preferable to have a shape ranging from a round sphere to a true sphere, and among them, a true sphere or a shape close to this is most preferable.
不定形粒子では、透明性樹脂への混合或いは透明性塗料
への混合時の分散性に劣る上、二次凝集による粒子の肥
大化で、沈降、沈殿を生じ、光学的均一性に欠は良好な
板状板や塗膜が得られない。Irregularly shaped particles have poor dispersibility when mixed into transparent resins or transparent paints, and the particles enlarge due to secondary aggregation, causing sedimentation and sedimentation, resulting in poor optical uniformity. A plate-like plate or coating film cannot be obtained.
真球形状の粒子であれば、この点の心配がなく良好な分
散性を示し光学的特性を大巾に改善する。True spherical particles do not have this problem, exhibit good dispersibility, and greatly improve optical properties.
とりわけ、真球形状又はそれに近い形状の粒子であれば
1本発明で特に好ましく採用するプレス延伸という板状
重合樹脂の二次加工(後述)時に粒子の二次凝集の発生
がなく、又粒子周辺に於ける重合体中の空隙(ボイド)
形成による光学的特性0.3μ〜/θμの範囲である。In particular, if the particles have a true spherical shape or a shape close to it, secondary aggregation of the particles will not occur during the secondary processing (described later) of the plate-shaped polymer resin, which is press stretching, which is particularly preferably employed in the present invention, and the periphery of the particles voids in polymers
The optical properties due to the formation range from 0.3μ to /θμ.
0.3μ未満の平均粒子径の粒子を用いると所望の光拡
散効率を得られない。又、/θμを超えると所望の光嶽
透過率が得られず、暗い光拡散板となる他、二次加工時
(二粒子周辺(:欠陥が生じやすく品質の一定した拡散
板が得られにくいという欠点を有する。好ましくは0.
3〜!μさら(二好ましくは0.j〜3μの範囲の平均
粒子径である。If particles having an average particle diameter of less than 0.3 μm are used, the desired light diffusion efficiency cannot be obtained. In addition, if /θμ is exceeded, the desired light transmittance cannot be obtained, resulting in a dark light diffuser plate, and during secondary processing (around two particles), defects are likely to occur and it is difficult to obtain a diffuser plate of consistent quality. Preferably 0.
3~! The average particle size is preferably in the range of 0.j to 3μ.
本発明において数平均粒子径の測定法は以下の条件で行
う。In the present invention, the number average particle diameter is measured under the following conditions.
測定装置:遠心式自動粒度分布測定装置(パーティクル
アナライザー)
(タイプ)CAPA−600型
(装置メーカー)日立1機製
測定方式:高速遠心沈降法と自然沈降法を採用した光透
過式液相沈降粒度分布測定法(二より数平均粒子径を算
出する。Measuring device: Centrifugal automatic particle size distribution measuring device (particle analyzer) (Type) CAPA-600 model (device manufacturer) Hitachi 1 unit Measuring method: Light transmission liquid phase sedimentation particle size distribution using high-speed centrifugal sedimentation method and natural sedimentation method Measurement method (calculate the number average particle diameter from 2.
分散媒体:界面活性剤水溶液
分散条件:超音波分散
シリコーン球状粒子の透明性樹脂への混合量は、最終的
に用いられる拡散板の板厚に応じて最適の濃度に設定さ
れるべきである。板厚が/〜3鴫と比較的厚い場合は、
/チ前後の比較的低濃度で、高透過で高拡散の拡散板が
得られる。一方、/θθμ〜20θμ程度の薄い板の場
合は20チ前後の混合量を必要とする。更に塗料4=シ
て透明基板の表面に塗布する場合、その塗膜厚は通常3
〜30μ程度となる為、粒子濃度としてはj0多前後と
なる。Dispersion medium: Aqueous surfactant solution Dispersion conditions: The amount of ultrasonically dispersed silicone spherical particles mixed into the transparent resin should be set to an optimal concentration depending on the thickness of the diffuser plate to be finally used. If the plate thickness is relatively thick, such as /~3mm,
A diffuser plate with high transmittance and high diffusion can be obtained with a relatively low concentration of around 1/2. On the other hand, in the case of a thin plate of about /θθμ to 20θμ, a mixing amount of about 20μ is required. Furthermore, when applying paint 4 to the surface of a transparent substrate, the coating film thickness is usually 3
Since the particle size is approximately 30μ, the particle concentration is approximately j0.
本発明では、透明性樹脂板にシリコーン球状粒子を分散
混合せしめ拡散板としたものも、又、透明性塗料にシリ
コーン球状粒子を分散混合せしめ、光拡散性塗料とし、
透明プラスチック基板、及びガラス基板の表面に塗布し
た拡散板も含まれる。In the present invention, silicone spherical particles are dispersed and mixed in a transparent resin plate to form a diffusion plate, and silicone spherical particles are dispersed and mixed in a transparent paint to form a light-diffusing paint.
Also included are transparent plastic substrates and diffuser plates coated on the surface of glass substrates.
本発明に用いられるシリコーン球状粒子の含水率は7〜
2俤と比較的高く、加熱加工する二次加工時に気泡とな
ったリポイドとなるトラブルを生じやすく、安定した品
質の拡散板を得られにくいという事に遭遇しやすい為透
明プラスチック材料に分散混合せしめる前に、充分に加
熱乾燥し含水率を低めて使用する事に留意する必要があ
る。The moisture content of the silicone spherical particles used in the present invention is 7 to
It is relatively expensive at 2 yen, and it is easy to cause problems such as lipoids forming bubbles during secondary processing by heating, and it is difficult to obtain a diffuser plate of stable quality. Therefore, it is dispersed and mixed in transparent plastic material. Before use, it is necessary to sufficiently heat and dry the product to lower the moisture content.
本発明に用いられる透明樹脂としては、メタアクリル樹
脂、ポリカーボネート樹脂、塩化ビニール樹脂、ポリス
チレン樹脂、ポリエステル樹脂等が好ましく採用され、
これら透明樹脂に、シリコーン球状粒子の所定量が押出
機等のシーテイング装置を使用して混合される。As the transparent resin used in the present invention, methacrylic resin, polycarbonate resin, vinyl chloride resin, polystyrene resin, polyester resin, etc. are preferably employed,
A predetermined amount of silicone spherical particles is mixed into these transparent resins using a sheeting device such as an extruder.
本発明において透明性樹脂板の厚さはその目的、樹脂の
種類などによって任意のものが用い得る。In the present invention, any thickness of the transparent resin plate can be used depending on the purpose, the type of resin, etc.
普通の条件では0./種以上のものが好ましく用いられ
る。しかじ後(二述べるようにプレス延伸による一次加
工によって物性を向上せしめたものは、0.1m未満の
ものも好適(二用い得る。0 under normal conditions. / species or more are preferably used. For those whose physical properties have been improved by primary processing by press stretching as described above, those with a length of less than 0.1 m are also suitable.
この内メタクリル樹脂は、七ツマーキャストによる重合
も可能な事からメタクリルモノマーにシリコーン粒子を
分散せしめた後重合して板とする方法も可能となる。Among these, methacrylic resin can be polymerized by seven-mer casting, so it is also possible to disperse silicone particles in methacrylic monomer and then polymerize it to form a plate.
本発明において、透明性樹脂の材料として特に好ましく
採用されるのは、メタクリル樹脂である。In the present invention, methacrylic resin is particularly preferably employed as the transparent resin material.
本発明で用い得るメタクリル樹脂はメチルメタクリレー
ト(以後MMAと略称)を主成分とする重合体であり、
MMA重合体(以後PMMAと略称)、MMAを含有す
る共重合体、PMMAあるいはMMA共重合体に他ポリ
マーを配合したポリマーブレンド、その他各種の配合物
を添加したもの等である。PMMAはセルキャスト法に
より容易Cニシート状に重合される。分子量も重量平均
分子量10θ万以上の超高分子量PMMAが容易に重合
でき、本発明では良好に使用できる。The methacrylic resin that can be used in the present invention is a polymer whose main component is methyl methacrylate (hereinafter abbreviated as MMA),
These include MMA polymers (hereinafter abbreviated as PMMA), copolymers containing MMA, polymer blends in which PMMA or MMA copolymers are blended with other polymers, and those in which various other blends are added. PMMA can be easily polymerized into C-sheets by cell casting. Ultra-high molecular weight PMMA having a weight average molecular weight of 100,000 or more can be easily polymerized and can be favorably used in the present invention.
MMA共重合体にはMMAとアルキルアクリレート共重
合体が良好に使用できる。アルキルアクリレートとして
メチルアクリレート、エチルアクリレート、プロピルア
クリレート、ブチルアクリレート、コーエチルへキシル
アクリレート等の7〜10重量%共重合体が良好に使用
できる。MMA−無水マレイン酸−スチレン3元系共重
合体、MMA−メチルメタアクリルアミド共重合体等の
耐熱アクリル樹脂も良好に使用できる。この他、MMA
とスチレン、スチレン誘導体、アクリロニトリル、メタ
クリレートリル、アクリル酸、メタクリル酸の7種ある
いは2種以上の共重合体が使用できる。メタクリル樹脂
は、他の透明性樹脂材料と比較し、透明度が高く、屋外
で使用しても黄変しにくいという耐候性に最も秀れた樹
脂であり、表面硬度、剛性という点に秀れている事によ
る。As the MMA copolymer, MMA and alkyl acrylate copolymers can be used favorably. As the alkyl acrylate, 7 to 10% by weight copolymers of methyl acrylate, ethyl acrylate, propyl acrylate, butyl acrylate, coethylhexyl acrylate, etc. can be used favorably. Heat-resistant acrylic resins such as MMA-maleic anhydride-styrene ternary copolymer and MMA-methylmethacrylamide copolymer can also be used satisfactorily. In addition, MMA
Seven or more copolymers of styrene, styrene derivatives, acrylonitrile, methacrylate, acrylic acid, and methacrylic acid can be used. Compared to other transparent resin materials, methacrylic resin has high transparency, is resistant to yellowing even when used outdoors, and has the best weather resistance.It also has excellent surface hardness and rigidity. Depends on being there.
しかしながら、メタクリル樹脂の欠点は、耐画撃性に劣
り、脆い点にあり、液晶デイスブンーのバックライト用
拡散板のような軽量性と薄さを強く求められる用途には
、採用されがたい情況にある。However, the disadvantages of methacrylic resin are that it has poor image impact resistance and is brittle, making it difficult to be used in applications that strongly require lightness and thinness, such as backlight diffusers for LCD displays. be.
従って本発明者は、このメタクリル樹脂の欠点を大巾に
改良する為にプレス延伸という延伸手法を二次加工とし
て採用しコ軸に分子配向強化する手段を積極的に採用す
る。Therefore, in order to greatly improve the drawbacks of this methacrylic resin, the present inventors actively employ a stretching method called press stretching as a secondary processing to strengthen the molecular orientation along the co-axis.
本発明の球状粒子が透明性樹脂に分散混合された拡散板
の機械的物性を向上せしめる為、プレス延伸という手法
を好ましく採用する。In order to improve the mechanical properties of a diffuser plate in which the spherical particles of the present invention are dispersed and mixed in a transparent resin, a method of press stretching is preferably employed.
すなわち、プレスで加熱押圧し薄肉化・高面積化し高度
分子配向せしめ、物性強化する方法を好ましく採用する
。That is, it is preferable to adopt a method of heating and pressing with a press to make the material thinner and have a larger area, resulting in highly oriented molecular orientation and strengthening the physical properties.
ここで、球状粒子として従来から用いられている有機系
の拡散剤(主としてポリスチレン粒子)を本発明の球状
粒子の代りに採用すると延伸前の原反の段階では、拡散
剤が球状粒子として透明樹脂中に分散していても、プレ
ス延伸の工程で粒形が変形し偏平粒子となり著しく光線
透過率を低減し又プレス延伸時の温度、プレス圧力、プ
レス速度等の条件に著しく粒形の変化が変動しバラツキ
が大きく一定の品質を有する光拡散板が安定に製造でき
ないという問題がある。しかし本発明の球状粒子を用い
ることにより、この不都合は解消される。Here, if an organic diffusing agent (mainly polystyrene particles) conventionally used as spherical particles is used instead of the spherical particles of the present invention, the diffusing agent becomes spherical particles in the transparent resin at the stage of the original fabric before stretching. Even if they are dispersed in the material, the grain shape is deformed during the press-stretching process and becomes flat particles, which significantly reduces the light transmittance.Also, the grain shape changes significantly depending on the conditions such as temperature, press pressure, and press speed during press-stretching. There is a problem that a light diffusing plate having a constant quality cannot be stably manufactured due to large fluctuations. However, by using the spherical particles of the present invention, this disadvantage is overcome.
本発明でいう、前記プレス延伸によるコ軸(二分子配向
されたメタクリル樹脂板(シート)の成形法としては、
特開昭60−2372/2号の圧縮成形法が好ましく使
用できる。In the present invention, the method of forming the co-axis (bimolecularly oriented methacrylic resin plate (sheet)) by press stretching is as follows:
The compression molding method disclosed in JP-A-60-2372/2 can be preferably used.
モしてコ軸配向シート(二は平均オリエンテーションリ
リースストレス(以後OR8と略称)がjにV−以上の
コ軸配向がかけられていることが好ましい。OR8はシ
ート配向度合を示し、シートを加熱した時の収縮力であ
る。OR8測定法はA8TMD/夕θりに準拠する。It is preferable that the co-axis oriented sheet (2 is the average orientation release stress (hereinafter abbreviated as OR8) is applied with a co-axis orientation of V- or more.OR8 indicates the degree of sheet orientation, and the sheet is heated. This is the contractile force when it is applied.The OR8 measurement method is based on A8TMD/Twilight θ.
本発明において用い得るメタクリル樹脂板(シート)は
平均OR8が!(値以上、好ましくは10〜4tOhz
−の強力なコ軸配向がかけられているものが特に好まし
い。メタクリル樹脂板(シート)はλ軸配向させること
(二より耐園撃度が強くなり、ORBがj l’v/i
以上、特に/ OKg/d l二なると耐爾撃強度は著
しく大きくなる。OR8と耐向撃強度との関係は特開昭
j♂−/7/りl1号に示されている。The methacrylic resin plate (sheet) that can be used in the present invention has an average OR8! (more than the value, preferably 10-4tOhz
Particularly preferred are those with a strong - co-axis orientation. The methacrylic resin plate (sheet) should be oriented along the λ axis (the impact resistance will be stronger than the second one, and the ORB will be j l'v/i
Above, especially when /OKg/dl2, the impact resistance becomes significantly large. The relationship between OR8 and counter-impact strength is shown in Japanese Patent Application Laid-open No. 11-11711.
ここに述べるコ軸配向とは、はぼコ軸方向に均一に配向
がかけられたもので、若干の2軸方向のOR8差、延伸
倍率の差があるものも含まれるものとする。全方向に均
等に配向がかけられた多軸配向板(シート)は本発明に
含まれ、最も良好1:使用できる。The co-axis orientation described herein refers to uniform orientation in the co-axis direction, and includes slight differences in OR8 in the two axes and differences in stretching ratio. A multiaxially oriented plate (sheet) that is evenly oriented in all directions is included in the present invention, and the best score is 1: it can be used.
このプレス延伸法を使用する事により、本来具備してい
るメタクリル樹脂の樹脂の特長である透明性、耐候性、
硬度、剛性を維持したまま最大の欠点である耐衝撃性を
大巾に改良する事が出来る。By using this press stretching method, methacrylic resin has the characteristics of transparency, weather resistance, and
It is possible to greatly improve impact resistance, which is the biggest drawback, while maintaining hardness and rigidity.
従ってメタクリル樹脂では従来不可能とされていた薄板
例えば0.7m未満のフィルム状のシートも良好(二側
用できるようになる。Therefore, thin sheets, for example, film-like sheets of less than 0.7 m, which were conventionally considered impossible to use with methacrylic resin, can be produced successfully (two-sided use).
又、プレス延伸法(二よるメタクリル樹脂板の特長とし
て、高度分子配向した樹脂板でありながら、光学的に極
めて均一であり光の複屈折が少ないという利点もあり、
偏光フィルムとの張り合せで使用する液晶デイスプレー
基板の用途、或いは光ディスクという高度の光学均一性
を要求される用途に使用できるという利点を有する。In addition, as a feature of the methacrylic resin plate using the press stretching method (2), although it is a highly molecularly oriented resin plate, it has the advantage that it is optically extremely uniform and has little birefringence of light.
It has the advantage that it can be used for applications such as liquid crystal display substrates used in lamination with polarizing films, or optical discs, which require a high degree of optical uniformity.
更にプレス延伸する事により、メタクリル樹脂のもう一
つの欠点である有機溶剤(二おかされやすいという性質
、有機布溶剤に接触すると細いクレージング発生し白化
し透明性が著しく低下するという性質も大巾(二改良さ
れるという利点も有する。Furthermore, by press-stretching, another disadvantage of methacrylic resin, which is that it is easily oxidized by organic solvents, and when it comes into contact with organic solvents, thin crazing occurs, whitening, and the transparency is significantly reduced, can be overcome. It also has the advantage of being improved.
この事により、使用中にほこりで汚れ洗浄する場合ある
いは夏場の殺虫剤松露という悪条件下にも耐えられると
いう利点も有する。This also has the advantage of being able to withstand harsh conditions such as when cleaning dirt and dust during use, or under harsh conditions caused by insecticide pine dew in the summer.
本発明において透明性樹脂(二対するシリコーン球状粒
子の混合については、一般に押出機でシーテイングする
時に所定量ブレンドされるが、メタクリル樹脂を用いる
場合はメタクリルモノマーを使用し、七ツマー中Cニシ
リコーン球状粒子を所定tn合し分散せしめ、その後二
枚のガラス板の間にこの分散モノマーを注入し、重合せ
しめ板状物どする手法を好ましく採用する。この理由は
、押出機混合分散より熱履歴が少なく、余分なトラブル
が少いという点、混合が容易であるという点の他、七ツ
マーキャスト(二よるメタクリル樹脂の分子機は/θO
万以上(押出板の分子量は10〜λθ万程度)と大きい
点から耐熱性、耐溶剤性に秀れたプレス延伸板が得られ
る所にある。更にレーザービームに切断加工、旋盤によ
る機械加工、ドリルによる穴あけ加工、更に溶剤や接着
剤による接着作業性という点でも、キャスト板からによ
る延伸板が秀れている点にもある。(組立作業に有利と
なる)
つぎに本発明の透明性塗料としては溶剤蒸発型のニトロ
セルロースラッカー、塩化ビニル樹脂塗料、アクリルラ
ッカー酸化重合型の油性調合ペイント、合成樹脂調合ペ
イント、フタル酸樹脂塗料、フェノール樹脂塗料、塩化
ゴム塗料、シリコーンアルキド樹脂塗料、付加重合型の
不飽和ポリエステル樹脂塗料、紫外線硬化塗料、電子線
硬化塗料、エポキシ樹脂塗料、ポリウレタン樹脂塗料(
ポリイソシアナート−ポリオール樹脂)、加熱縮合重合
型のアミノアルキド樹脂塗料、アミノアクリル樹脂塗料
、アミノポリエステル樹脂塗料、シリコンポリエステル
樹脂塗料などが使用できる。In the present invention, transparent resin (2 pairs of silicone spherical particles are generally blended in a predetermined amount during sheeting with an extruder, but when using a methacrylic resin, a methacrylic monomer is used, Preferably, a method is adopted in which particles are mixed and dispersed to a predetermined tn, and then the dispersed monomer is injected between two glass plates, and polymerized to form a plate-like product.The reason for this is that the thermal history is smaller than that of extruder mixing and dispersion. In addition to the fact that there are few extra troubles and easy mixing, the molecular machine of methacrylic resin is
Since the molecular weight of the extruded plate is as high as 10,000 or more (the molecular weight of the extruded plate is about 100,000 to λθ), it is possible to obtain a press-stretched plate with excellent heat resistance and solvent resistance. Furthermore, stretched plates made from cast plates are superior in terms of ease of cutting with a laser beam, machining with a lathe, drilling with a drill, and adhesion with a solvent or adhesive. (It is advantageous for assembly work) Next, the transparent paints of the present invention include solvent evaporation type nitrocellulose lacquer, vinyl chloride resin paint, acrylic lacquer oxidation polymerization type oil-based paint, synthetic resin paint, and phthalate resin paint. , phenolic resin paint, chlorinated rubber paint, silicone alkyd resin paint, addition polymerization type unsaturated polyester resin paint, ultraviolet curing paint, electron beam curing paint, epoxy resin paint, polyurethane resin paint (
Polyisocyanate-polyol resin), heat condensation polymerization type amino alkyd resin paint, amino acrylic resin paint, amino polyester resin paint, silicone polyester resin paint, etc. can be used.
上記塗料のうち本発明においてはとくに光学的性質が要
求されるという点から塗膜の透明性に可能な限り優れて
いるものを選定する事が必要である。更にシリコーン樹
脂粒子の分散性、塗装加工性に優れている塗料である事
が好ましい。父、耐候性、耐擦傷性、耐薬品性、耐溶剤
性等にすぐれている事も要求される。Among the above-mentioned paints, it is necessary to select one that has the best possible coating film transparency since optical properties are particularly required in the present invention. Furthermore, it is preferable that the coating material has excellent dispersibility of silicone resin particles and coating processability. Moreover, it is also required to have excellent weather resistance, scratch resistance, chemical resistance, solvent resistance, etc.
本発明においては、上記観点より主として耐擦傷性を恵
視し、紫外線硬化型アクリル樹脂塗料、熱硬化型シリコ
ーン樹脂塗料、ポリワレタン樹脂塗料を好ましく使用す
る。In the present invention, from the above-mentioned viewpoint, consideration is given mainly to scratch resistance, and ultraviolet curable acrylic resin paints, thermosetting silicone resin paints, and polyurethane resin paints are preferably used.
これら塗料にさらに必要に応じて溶剤を追加混合し、粘
度調整し、膜形成能、塗工性能を高めるのが通常である
。使用される溶剤の種類、混合量は、採用する塗工方法
、目的とする塗膜厚さ、使用する塗膜形成材料の種類、
乾燥方法、硬化方法とその条件等によって適正の塗料、
混合量が決定される。本発明ではシリコーン球状粒子が
、透明性塗料中に存在する壁膜形成材料(二対して/〜
r o wts混合分散せしめられる。It is usual to add a solvent to these paints as necessary to adjust the viscosity and improve film-forming ability and coating performance. The type and amount of solvent used depends on the coating method used, the desired coating thickness, the type of coating film forming material used,
Appropriate paint, depending on drying method, curing method and conditions, etc.
The amount of mixture is determined. In the present invention, silicone spherical particles are used as wall film-forming materials (2 to 2) present in transparent paints.
r o wts mixed and dispersed.
シリコーン球状粒子の透明性塗料への分散は、塗膜形成
材料に直接混合分散せしめる事も可能であり、父、塗膜
形成材料と溶剤との混合液つまり塗料中に混合分散せし
める事も可能である。Silicone spherical particles can be dispersed in a transparent paint by mixing and dispersing them directly into the paint film forming material, or by mixing and dispersing them into a mixture of the paint film forming material and a solvent, that is, the paint. be.
かくして得られたシリコーン球状粒子が混合分散された
透明性塗料は透明基板の表面にスプレー法、ディッピン
グ法、カーテンフロー法、ロールコータ−法、印刷法等
の手段を用いて塗布され、紫外線照射装置又は加熱で硬
化せしめる方法が用いられる。The thus obtained transparent paint in which silicone spherical particles are mixed and dispersed is applied to the surface of a transparent substrate using a spray method, dipping method, curtain flow method, roll coater method, printing method, etc., and then applied using an ultraviolet irradiation device. Alternatively, a method of curing by heating may be used.
透明性塗料の塗膜形成材料として使用する透明性樹脂の
種類については本発明で特に制限するものではない。但
し、前記した本発明による拡散板の各種用途で採用され
た場合の使用環境を考慮すると、耐候性に優れ、且つ表
面硬度に秀れた塗料が求められる事から、表面硬化性透
明塗料が特に望ましい。The present invention does not particularly limit the type of transparent resin used as the coating film forming material of the transparent paint. However, considering the usage environment in which the diffuser plate of the present invention is used in various applications, a coating material with excellent weather resistance and surface hardness is required, and surface-curing transparent coating materials are particularly preferred. desirable.
一般に表面硬化性透明塗料とは、透明合成樹脂の表面に
コーティングして合成樹脂表面を硬くし、耐擦傷性を向
上させる1〜50μm厚の薄い透明硬化層であり、多官
能アクリレート系リジッドコート層、ポリオルガノシロ
キサン系リジッドコート層が一般に広く使用されており
、本発明に於ても良好に使用できる。表面硬化層は鉛筆
硬度で98以上が好ましく、更に好ましくはjH以上で
ある。In general, a surface-curing transparent paint is a thin transparent cured layer with a thickness of 1 to 50 μm that is coated on the surface of a transparent synthetic resin to harden the synthetic resin surface and improve scratch resistance.It is a polyfunctional acrylate rigid coating layer. Polyorganosiloxane rigid coat layers are generally widely used and can be used satisfactorily in the present invention. The surface hardening layer preferably has a pencil hardness of 98 or more, more preferably jH or more.
ここに述べる多官能アクリレート系表面硬化層は、多官
能アクリレート系化合物を主成分とした多官能アクリレ
ート系表面硬化塗料を合成樹脂基材表面Cニデイツビン
グ法、スピン法、スプレー法、カーテンフロー法等の方
法でコーティングした後、主(二紫外線照射により硬化
させて形成させたものである。The polyfunctional acrylate surface hardening layer described here is a polyfunctional acrylate surface hardening paint containing a polyfunctional acrylate compound as a main component, which is applied to the surface of a synthetic resin substrate using a coating method, a spin method, a spray method, a curtain flow method, etc. It is formed by coating it by a method and then curing it by irradiating it with two ultraviolet rays.
多官能アクリレート系化合物は分子の末端または側鎖に
複数個のアクリロイルオキシまたはメタクロイルオキシ
基(CH2=CR−α幻−1RはHまたはCH,)を有
する化合物であり、一般にオリゴアクリレートとも呼ば
れるものである。多官能アクリレート化合物の例を第7
表に示す。Polyfunctional acrylate compounds are compounds that have multiple acryloyloxy or methacryloyloxy groups (CH2=CR-αphantom-1R is H or CH,) at the end or side chain of the molecule, and are also generally called oligoacrylates. It is. Examples of polyfunctional acrylate compounds are shown in Section 7.
Shown in the table.
これ等の多官能アクリレート化合物のうち、ペンタエリ
スリトール系アクリレート等の空気中での紫外線硬化性
に優れた化合物が特に良好に使用できる。Among these polyfunctional acrylate compounds, compounds with excellent UV curability in air, such as pentaerythritol acrylate, can be used particularly well.
紫外線硬化の為に多官能アクリレート系表面硬化塗料に
は、ベンゾフェノン系あるいはアセトフェノン系物質で
代表される光重合開始剤又は光増感剤が添加される。ま
た、必要に応じて各種添加剤例えば酸化防止剤、光安定
剤、熱重合防止剤、紫外線吸収剤等の安定剤、着色剤、
塗膜の平滑性付与の為のフッ素系あるいはシリコン系等
の界面活性剤等が少量添加される。For UV curing, a photopolymerization initiator or photosensitizer, typically a benzophenone or acetophenone substance, is added to a multifunctional acrylate surface-curing coating. In addition, various additives such as antioxidants, light stabilizers, thermal polymerization inhibitors, stabilizers such as ultraviolet absorbers, colorants,
A small amount of a fluorine-based or silicon-based surfactant is added to give the coating film smoothness.
ポリオルガノシロキサン系リジッドコート層としては、
メチルトリアルコキシシランとフェニルトリアルコキシ
シランとを出発原料とするもの、これにテトラアルコキ
シシランを組合せたもの、あるいは他の樹脂塗料との混
合物等、例えはメチルトリエトキシシラン/フェニルト
リエトキシシラン反応混合物(U8P 34tsl♂
3♂)、メチルトリエトキシシランの部分加水分解物/
酢酸/ナフテン酸ソーダ(特開昭jθ−/13rs2)
、メチルトリメトキシシラン/テトラエトキシシラン/
両末端水酸基性ジメチルポリシロキサン/酸性触媒反応
混合物(特開昭30−//≦g00)、テトラアルコキ
シシラン加水分解物/アルキルトリアルコキシシラン加
水分解物/有機カルボン酸のアルカリ金属塩混合物(特
開昭グ♂−st、z3o)等があり、又、ビニル基、エ
ポキシ基、アミノ基等の官能基を有するポリオルガノシ
ロキサンを出発原料とするもの、例えば、ビニルアルコ
キシシランと酢酸ビニルとの共重合体の加水分解物/ア
ルキルシリケートの加水分解物/酢酸ビニル又はアクリ
ル酸、メタクリル酸、そのエステル類/三フッ化ホウ素
モノエチルアミンコンプレックス(特開昭グ♂−2乙2
2/)、r−グリシドキシアルキルトリアルコキシシラ
ンの開環重合物(特開昭jθ−グ0674t)、β−(
3,4t−エポキシシクロヘキシル)エチルトリメトキ
シシラン、γ−メタクリロキシプロピルトリメキシシラ
ン、ビニルトリメトキシシランの7種又コ種以上の反応
混合物(特開昭to−tq/24t)、β−(3,<を
−エポキシシクロヘキシル)エチルトリメトキシシラン
、r−メタクリロキシプロピルトリメトキシシラン、ビ
ニルトリメトキシシランの7種又は一種以上とエポキシ
プリポリマー、ジアリルフタレート、グリシジルメタク
リレートなどとの反応混合物(特開昭3−0−69/7
4t)、(コ、3−エボキシプロボキシ)メチルトリメ
トキシシラン/グリシジルメタクリレート反応混合物(
特開昭!θ−7♂乙3り)、アミノアルキルアルコキシ
シラン/エポキシアルキルアルコキシシラン部分加水分
解反応混合物(特開昭4t♂−♂4t♂7♂)等が使用
できる。As a polyorganosiloxane rigid coat layer,
Those using methyltrialkoxysilane and phenyltrialkoxysilane as starting materials, those in combination with tetraalkoxysilane, or mixtures with other resin coatings, such as methyltriethoxysilane/phenyltriethoxysilane reaction mixtures. (U8P 34tsl♂
3), partial hydrolyzate of methyltriethoxysilane/
Acetic acid/sodium naphthenate (JP-A-Shojθ-/13rs2)
, methyltrimethoxysilane/tetraethoxysilane/
Hydroxyl-terminated dimethylpolysiloxane/acidic catalytic reaction mixture (JP-A-30-//≦g00), tetraalkoxysilane hydrolyzate/alkyltrialkoxysilane hydrolyzate/alkali metal salt mixture of organic carboxylic acid (JP-A There are also polyorganosiloxanes containing functional groups such as vinyl groups, epoxy groups, amino groups, etc., such as copolymerization of vinyl alkoxysilane and vinyl acetate. Combined hydrolyzate/Alkyl silicate hydrolyzate/Vinyl acetate or acrylic acid, methacrylic acid, and their esters/Boron trifluoride monoethylamine complex (JP-A Shogu ♂-2 Otsu 2
2/), ring-opening polymer of r-glycidoxyalkyltrialkoxysilane (Japanese Patent Application Laid-Open No. 2006-0674t), β-(
Reaction mixture of seven or more types of 3,4t-epoxycyclohexyl)ethyltrimethoxysilane, γ-methacryloxypropyltrimexysilane, and vinyltrimethoxysilane (JP-A-Sho-tq/24t), β-(3 , <-epoxycyclohexyl) ethyltrimethoxysilane, r-methacryloxypropyltrimethoxysilane, vinyltrimethoxysilane, and a reaction mixture of epoxy prepolymer, diallyl phthalate, glycidyl methacrylate, etc. 3-0-69/7
4t), (co,3-epoxyproboxy)methyltrimethoxysilane/glycidyl methacrylate reaction mixture (
Tokukai Akira! θ-7♂Otsu 3), aminoalkylalkoxysilane/epoxyalkylalkoxysilane partial hydrolysis reaction mixture (JP-A No. 4T♂-♂4T♂7♂), etc. can be used.
これら表面硬化性透明塗料を塗布し、紫外線硬化又は加
熱硬化する前にシリコーン球状粒子をホモミキサー等で
混合分散せしめる。混合に当っては、空気等の気泡が生
じないよう真空系で混合する或いは混合後、真空系で脱
胞する事が望ましい、或いは消泡剤等を併用して混合す
る事も望ましい。These surface-curing transparent coatings are applied, and before being cured by ultraviolet light or heat, silicone spherical particles are mixed and dispersed using a homomixer or the like. When mixing, it is preferable to mix in a vacuum system to prevent the formation of air bubbles, or to remove bubbles in a vacuum system after mixing, or it is also desirable to use an antifoaming agent or the like in combination.
いずれにしても混合液に気泡が混入していると、塗付工
程に於て、あるいは硬化後の拡散板の光学特性について
バラツキが生じ安定な生産ができなくなる。In any case, if air bubbles are mixed into the liquid mixture, there will be variations in the optical properties of the diffuser plate during the coating process or after curing, making stable production impossible.
表面硬化性透明塗料へのシリコーン球状粒子の添加量は
塗膜厚さと、最終製品(拡散板)に要求される光学特性
(全光線透過率、拡散光線率)に応じて決定されるが、
その混合量は塗料中の塗膜形成材料に対して重量係でT
h/〜r o wtt4の範囲である。7 wt%未満
だと拡散光率が低く、!θwt4を超えると混合時(ニ
二次凝集し均一分散が出来なくなる恐れがある。かくし
て得られた塗料を透明基板の片面あるいは両面に所定の
塗布法でコーティングする。The amount of silicone spherical particles added to the surface-curing transparent paint is determined depending on the coating thickness and the optical properties (total light transmittance, diffused light rate) required for the final product (diffusion plate).
The mixing amount is T based on the weight of the film forming material in the paint.
It is in the range of h/~r o wtt4. If it is less than 7 wt%, the diffused light rate will be low! If θwt4 is exceeded, there is a risk of secondary agglomeration during mixing (secondary agglomeration), making it impossible to achieve uniform dispersion.The paint thus obtained is coated on one or both sides of a transparent substrate using a predetermined coating method.
透明基板としては、メタクリル樹脂、ポリカーボネート
樹脂、ポリエステル樹脂、ポリ塩化ビニル樹脂、ポリス
チレン等の透明性プラスチック樹脂板が使用できる他、
ガラス板のような無機質透明板の採用も可能である。特
に、全光線透過率、拡散光線率が例えばりθ慢以上要求
するような高度な用途には、メタクリル樹脂板とガラス
板が最も望しく採用される。こ\でメタクリル樹脂とし
ては、さき(二特許請求の範囲第1項のために詳細(:
説明した透明性樹脂に用いるメタクリル樹脂もすべて用
い得る。As the transparent substrate, transparent plastic resin plates such as methacrylic resin, polycarbonate resin, polyester resin, polyvinyl chloride resin, and polystyrene can be used.
It is also possible to use an inorganic transparent plate such as a glass plate. In particular, methacrylic resin plates and glass plates are most preferably employed in advanced applications where total light transmittance and diffused light rate are required to be, for example, greater than θ. Here, the methacrylic resin is described below (detailed for the purpose of claim 1):
All of the methacrylic resins used in the transparent resins described may also be used.
塗料の塗布方法について、拡散板の用途、要求性能、経
済性を考慮し最適な方法が選択されるべきである。一般
に塗料の塗布方法としてスプレー塗装法、ディッピング
法、カーテンフロー法、ロールコータ−法、スピンコー
ティング法、スクリーン印刷法、グラビア印刷法、オフ
セット印刷法。Regarding the method of applying the paint, the optimum method should be selected in consideration of the use of the diffuser plate, required performance, and economical efficiency. Generally, coating methods include spray coating, dipping, curtain flow, roll coater, spin coating, screen printing, gravure printing, and offset printing.
バット印刷性等幾多の方法があり、いずれの方法も採用
可能である。但し、いずれの塗布方法を採用するにして
も、コーティング加工性、作業性、品質の安定性という
観点で、塗料の粘度(二制限があり、適性な粘度に塗料
を調整する必要がある。There are many methods such as bat printability, and any method can be adopted. However, no matter which application method is adopted, there are two restrictions on the viscosity of the paint from the viewpoint of coating processability, workability, and quality stability, and it is necessary to adjust the paint to an appropriate viscosity.
スピンコード法、スプレー塗装法、オフセット印刷法等
は比較的低粘度である事が要求され、適性な溶剤で、混
合塗料を適性粘度に希釈しておく必要がある。Spin code methods, spray coating methods, offset printing methods, etc. require relatively low viscosity, and it is necessary to dilute the mixed paint to an appropriate viscosity with an appropriate solvent.
又、得ようとする塗膜厚(二よっても粘度を溶剤で調整
する必要性が応々にして生じてくる。使用する溶剤につ
いても、コーティング中(二粘度が経時的に変化する事
が極めて不都合な事が多く、比較的高沸点溶剤が使用さ
れるケースが多いが、塗布後の溶剤乾燥(二時間を要し
たり、或いは、溶剤を少量含んだまま紫外線硬化したり
、加熱硬化したりすると、塗膜の硬度が著しく低下する
事C:相過する事になり、個々の塗料組成、塗布方法、
硬化方法等の各因子を充分留意して選択する必要がある
。更に、溶剤の選定については、透明基板と塗膜との密
着性に溶剤が微妙な影響を及ぼすので、この点からも選
定には充分の注意を要する。本発明者が、好ましく採用
する透明基板はメタクリル板とガラス板であり、これら
基板と塗膜との密着性に充分な強度が確保しにくい材料
である。Also, depending on the coating thickness you are trying to obtain, it may be necessary to adjust the viscosity with a solvent. There are many inconveniences, and relatively high boiling point solvents are used in many cases. As a result, the hardness of the paint film will decrease significantly.
It is necessary to carefully consider various factors such as the curing method when selecting the material. Further, regarding the selection of the solvent, since the solvent has a subtle influence on the adhesion between the transparent substrate and the coating film, sufficient care must be taken in the selection from this point of view as well. The transparent substrates preferably adopted by the present inventor are a methacrylic plate and a glass plate, and these materials are difficult to ensure sufficient strength for adhesion between the substrate and the coating film.
これら密着性に不安のある材料には、塗料を塗布する前
に適性な前処理或いはプライマー処理をするのが望まし
い。It is desirable that materials with poor adhesion be subjected to appropriate pretreatment or primer treatment before coating with paint.
かくのごとく、透明基板に塗布した後は溶剤を充分乾燥
揮発せしめた後、紫外線照射或いは加熱させ硬化せしめ
所望の拡散板とする。After coating on a transparent substrate in this way, the solvent is sufficiently dried and volatilized, and then cured by ultraviolet irradiation or heating to form the desired diffusion plate.
かくして得られた拡散板の光学特性は、ASTMD10
03の試験法に従い全光線透過率、拡散光線率、平行光
線率、ヘーズを測定する。The optical properties of the diffuser plate thus obtained are as per ASTM D10.
Measure the total light transmittance, diffused light rate, parallel light rate, and haze according to the test method of No. 03.
〈実施例〉 以下実施例で本発明の詳細な説明する。<Example> The present invention will be explained in detail below with reference to Examples.
実施例/
シリコーン系球状粒子として、珪素原子に3ヶの加水分
解性官能基と、/ケのメチル基とを有する原料シランを
加水分解反応し、次いで縮合反応して微粒子化とした網
状構造体をなしかつ固体状の球状粒子を使用した。Example: A network structure obtained by hydrolyzing a raw material silane having three hydrolyzable functional groups and / of methyl groups on a silicon atom and then condensing it to form fine particles as silicone-based spherical particles. Solid spherical particles were used.
該シリコーン系球状粒子は、出発原料からして当然珪素
原子に結合する有機基はメチル基であり、その数は7ケ
である。このものの商品名はトスパール/、、20(東
芝シリコーン製)として市販されておりn−へキチン分
散液の粘度がj 70 CpSでした。In the silicone-based spherical particles, the organic groups bonded to silicon atoms in the starting materials are naturally methyl groups, and the number of these groups is seven. The product name of this product is Tospar/20 (manufactured by Toshiba Silicone), and the viscosity of the n-hechitin dispersion was J 70 CpS.
トスパール/2θは第2図のよう艦二個々の粒径が極め
てよく揃った球状単分散の微粒子である事がわかる。As shown in Figure 2, Tospearl/2θ is found to be spherical monodisperse fine particles with extremely uniform individual particle sizes.
トスパール/20の粒度分布を第3図(二示した。The particle size distribution of Tospearl/20 is shown in Figure 3.
第3図に示した如く、トスバールノコ0は比較的狭い粒
度分布を持った粒子でありその平均粒径は2μである。As shown in FIG. 3, Tosvar Saw 0 has particles with a relatively narrow particle size distribution, and its average particle size is 2μ.
比較例として、光拡散剤に硫酸パリューム(平均粒径3
μ)を使用した。トスパール/20及び硫酸バリウムを
グθθ〜6θ0センチボイズのメタクリルプレポリマー
にホモミキサーで分散させ。As a comparative example, parium sulfate (average particle size 3) was used as a light diffusing agent.
μ) was used. Tospearl/20 and barium sulfate were dispersed in a methacrylic prepolymer having a centivoid size of 6θ to 6θ0 using a homomixer.
重量調整の段階で30θ〜3jOセンチボイズとして2
枚のガラス製型板の間に注入を行ない製板とした。重合
は重合開始剤0.03 %添加し!Q℃で重合を開始さ
せ、その後//♂℃で後キユアリングしてプレス延伸用
原反とした。2 as 30θ~3jO centiboise at the stage of weight adjustment
A plate was made by pouring between two glass templates. During polymerization, 0.03% of polymerization initiator was added! Polymerization was started at Q°C, and then post-curing was performed at ♂°C to obtain an original fabric for press stretching.
トスパール7.20の添加量は、0.!1/、コ、夕の
4を種類、硫酸パリクムの添加量はコ、!俤、プレス延
伸用原反厚みは!■!とした。The amount of Tospearl 7.20 added was 0. ! 1/, ko, type 4 of evening, the amount of paricum sulfate added is ko,! What is the thickness of the original film for press stretching? ■! And so.
次いで、該プレス延伸用原板な/4tθ℃に予熱し30
0トンプレスを用いてプレス延伸を実施した。延伸倍率
は5倍、延伸後の板厚は/■Tとした。Next, the original plate for press stretching was preheated to /4tθ°C and heated to 30°C.
Press stretching was performed using a 0 ton press. The stretching ratio was 5 times, and the plate thickness after stretching was /■T.
この延伸板の光学特性を次の試験法で測定した。The optical properties of this stretched plate were measured using the following test method.
全光線透過率(T) ASTM D/θθ3拡散光
線透過率(IyI′)
平行光線透過率(PT)
ヘーズ(H)
色温度 JIS Z♂72!光学特性測
定の結果は第2表に示した。Total light transmittance (T) ASTM D/θθ3 diffused light transmittance (IyI') Parallel light transmittance (PT) Haze (H) Color temperature JIS Z♂72! The results of optical property measurements are shown in Table 2.
比較例として、従来の有機質光拡散剤(ポリスチレン粒
子)を添加したメタアクリルキャスト板による0.!1
丁拡散板である他社市販品2種の光学特性をも第7表(
二示した。As a comparative example, a conventional methacrylic cast plate containing an organic light diffusing agent (polystyrene particles) was used. ! 1
The optical properties of two commercially available diffuser plates from other companies are also shown in Table 7 (
I showed you two.
第2表の結果を明確にする為に平行光線透過率を横軸(
二全光線透過率を縦軸にプロットし図示したのが第9図
である。全光線透過率(T)、拡散光線透過率(DT)
、平行光線透過率(PT)及びヘーズ(H)の間Cニ
一般(二次の関係式が成立する。In order to clarify the results in Table 2, parallel light transmittance is plotted on the horizontal axis (
FIG. 9 shows the total light transmittance plotted on the vertical axis. Total light transmittance (T), diffuse light transmittance (DT)
, parallel light transmittance (PT), and haze (H).
T = DT + PT
H= DT/PT X 100
第y図の横軸にFTをプロットしたのはわずか/チのF
T値の違いであっても、実際に眼と光源の間に拡散板を
置いた時、光源の輪郭が明瞭に見えるかどうかに大きな
差異が認められる事による。T = DT + PT H = DT/PT
Even if there is a difference in T value, there is a large difference in whether the outline of the light source can be clearly seen when a diffuser plate is actually placed between the eye and the light source.
スナわち、液晶カラーテレビのバックライト用拡散板と
して使用する場合は平行光線透過率は/係でも低く、且
つ全光線透過率が/%でも高い特性を有する拡散板が要
求される。In other words, when used as a backlight diffusion plate for a liquid crystal color television, a diffuser plate is required that has a parallel light transmittance as low as /% and a total light transmittance as high as /%.
第9図より理解されるようにトスパール/2θを光拡散
剤として用いた拡散板が従来品(比較例)と比較し極め
て秀れた性質を有していると云える。As can be understood from FIG. 9, it can be said that the diffusion plate using Tospar/2θ as a light diffusing agent has extremely superior properties compared to the conventional product (comparative example).
一方、色温度も、特に液晶カラーテレビの用途では高い
事が要求される。一般に色温度が低いと赤味、黄味がか
つて見える、色温度が高いと青白く見える。液晶カラー
テレビの場合、バックライトからの光を液晶セルを通し
、赤、緑、青の三原色のフィルターを通してフルカラー
表示とする。On the other hand, the color temperature is also required to be high, especially for use in liquid crystal color televisions. In general, when the color temperature is low, a reddish or yellowish tinge appears, and when the color temperature is high, it appears pale. In the case of an LCD color TV, the light from the backlight passes through the liquid crystal cell and is filtered through the three primary colors of red, green, and blue to produce a full-color display.
従ってバックライトの色温度が低いと、三原色フィルタ
ーの色を忠実に投影させることができなくなり、くすん
だ色となる事からこの色温度は極めて重視される。一般
に液晶カラーテレビ用途としては6000°に以上の色
温度が要求され本発明による実施例の拡散板はこの点で
極めている事が理解できる。Therefore, if the color temperature of the backlight is low, the colors of the three primary color filters cannot be faithfully projected, resulting in dull colors, so this color temperature is extremely important. Generally, a color temperature of 6000° or higher is required for use in liquid crystal color televisions, and it can be seen that the diffuser plate of the embodiment of the present invention is extremely superior in this respect.
(以下余白)
第2表
5倍延伸
実施例2
イソプロピルアルコール主成分の溶剤で希釈したアクリ
ル系表面硬化透明塗料(早用塗料製品所製、商標G11
tter UVaoo−<tr)にシリコン系球状粒子
(東芝シリコーン製、商標トスパール/20)と硫酸バ
リクム(平均粒径3μm)をそれぞれ2θwt%添加し
、攪拌機で混合分散させた。(Margin below) Table 2 5x stretching Example 2 Acrylic surface hardening transparent paint diluted with a solvent mainly composed of isopropyl alcohol (manufactured by Hayayo Toyo Seishin Co., Ltd., trademark G11)
2θwt% of each of silicon-based spherical particles (manufactured by Toshiba Silicone, trademark Tospar/20) and baricum sulfate (average particle size 3 μm) were added to UVaoo-<tr) and mixed and dispersed using a stirrer.
次いで、該塗料を板厚7.2■の透明のメタクリル樹脂
シート(層化成製、商標プラグラスA ) t:片面ス
プレー塗装して紫外線硬化処理°した。Next, the paint was spray-painted on one side of a transparent methacrylic resin sheet (trade name: Plaglass A, manufactured by Layer Kasei Co., Ltd.) with a thickness of 7.2 cm, and subjected to ultraviolet curing treatment.
シリコン系球状粒子を添加した塗料で塗装したメタクリ
ル樹脂シートは、硫酸バリウムを添加したものに比べて
、実施例/の延伸板と同様に、全 6光線透過率が高く
、拡散光線透過率が高い高透過高拡散特性と高い色温度
特性を有する優れた光学特性を示した。この光学特性を
第3表(二示す。A methacrylic resin sheet coated with a paint containing silicon-based spherical particles has a higher total ray transmittance and a higher diffused ray transmittance, similar to the stretched sheet in Example/, compared to a sheet coated with a paint containing barium sulfate. It exhibited excellent optical properties with high transmittance, high diffusion properties, and high color temperature properties. These optical properties are shown in Table 3.
第 3 表 度 t。Table 3 Every time t.
)O
〈発明の効果〉
本発明によって得られる光拡散板は、従来のものに比し
全光線透過率を高めること\平行光線透過率を低めるご
、ととを同時にかつバランスよくとることに成功したも
のである。)O <Effects of the Invention> The light diffusing plate obtained by the present invention has succeeded in simultaneously increasing the total light transmittance and decreasing the parallel light transmittance in a well-balanced manner compared to conventional ones. This is what I did.
又、最近の液晶デイスプレー、液晶カラーテレビなどの
拡散板に要求される色温度、輝度分布などの特性も、充
分、本発明(二よって達成され得る。Further, the characteristics such as color temperature and brightness distribution required for the diffusion plates of recent liquid crystal displays and liquid crystal color televisions can be fully achieved by the present invention.
同粒子の粒度分布図、第7図は本発明および比較例の光
拡散板の特性図の例である。
特許出願人 旭化成工業株式会社
第1図
球a前子の令千槍■tデ゛ル
第2図
にスバール120の電子顕撤俵5真暢
第3図
粒子径 μm
トスバール+20の粒度分布The particle size distribution diagram of the same particles, FIG. 7, is an example of a characteristic diagram of light diffusing plates of the present invention and a comparative example. Patent Applicant: Asahi Kasei Industries, Ltd. Figure 1 Ball a Maeko Reisenyari ■ T Dale Figure 2 Subaru 120 Electron Microscope 5 Shinnobu Figure 3 Particle Size μm Tosvall +20 Particle Size Distribution
Claims (1)
和性を有する有機基が直結したポリシロキサン結合をな
す固体状のシリコーン樹脂からなる数平均粒子径0.3
〜10μの球状粒子が透明性樹脂板中に該透明性樹脂に
対して1〜50wt%混合、分散されて存在することを
特徴とする光透過性を有する光拡散板 2 珪素原子に透明性塗料中の塗膜形成材料又はそのモ
ノマーに対する親和性を有する有機基が直結したポリシ
ロキサン結合をなす固体状のシリコーン樹脂からなる数
平均粒子径0.3〜10μの球状粒子を透明性塗料中に
、該塗料中の前記塗膜形成材料又はそのモノマーに対し
て1〜50wt%混合分散せしめ、該塗料を透明基板の
少くとも片側に塗布したことを特徴とする光透過性を有
する光拡散板[Scope of Claims] 1. A number average particle size of 0.3 consisting of a solid silicone resin forming a polysiloxane bond in which an organic group having an affinity for a transparent resin or its monomer is directly bonded to a silicon atom.
A light diffusing plate 2 having light transmittance, characterized in that spherical particles of ~10μ are present in a transparent resin plate mixed and dispersed in an amount of 1 to 50 wt% based on the transparent resin.A transparent coating on silicon atoms. Spherical particles with a number average particle diameter of 0.3 to 10 μ made of a solid silicone resin with a polysiloxane bond directly connected to an organic group having an affinity for the coating film-forming material or its monomer are placed in a transparent paint. A light diffusing plate having light transmittance, characterized in that 1 to 50 wt% of the coating film forming material or its monomer is mixed and dispersed in the coating material, and the coating material is coated on at least one side of a transparent substrate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62329945A JPH01172801A (en) | 1987-12-28 | 1987-12-28 | Light diffusion plate having light transmittability |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62329945A JPH01172801A (en) | 1987-12-28 | 1987-12-28 | Light diffusion plate having light transmittability |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01172801A true JPH01172801A (en) | 1989-07-07 |
JPH0516002B2 JPH0516002B2 (en) | 1993-03-03 |
Family
ID=18227018
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62329945A Granted JPH01172801A (en) | 1987-12-28 | 1987-12-28 | Light diffusion plate having light transmittability |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01172801A (en) |
Cited By (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02194058A (en) * | 1989-01-21 | 1990-07-31 | Kyowa Gas Chem Ind Co Ltd | Light-diffusing synthetic resin |
JPH0353059U (en) * | 1989-09-28 | 1991-05-22 | ||
JPH03167269A (en) * | 1989-11-27 | 1991-07-19 | Matsushita Electric Works Ltd | Milk-white coating composition |
JPH0573602U (en) * | 1991-10-09 | 1993-10-08 | 恵和商工株式会社 | Light diffusion sheet material |
FR2694641A1 (en) * | 1992-08-10 | 1994-02-11 | Bridgestone Corp | Photodispersing material and its manufacturing process. |
JPH0667003A (en) * | 1992-08-20 | 1994-03-11 | Fuji Photo Film Co Ltd | Light diffusion plate |
JPH07216328A (en) * | 1994-02-04 | 1995-08-15 | Kimoto & Co Ltd | Light-diffusing pressure-sensitive adhesive composition |
WO1996013381A1 (en) * | 1994-10-31 | 1996-05-09 | Dai Nippon Printing Co., Ltd. | Decorative material having abrasion resistance |
JPH11109112A (en) * | 1997-10-02 | 1999-04-23 | Nippon Synthetic Chem Ind Co Ltd:The | Manufacture of glare preventive treated layer |
US5899552A (en) * | 1993-11-11 | 1999-05-04 | Enplas Corporation | Surface light source device |
JP2000098107A (en) * | 1998-09-24 | 2000-04-07 | Kimoto & Co Ltd | Forward scattering film |
US6322225B1 (en) | 1993-12-17 | 2001-11-27 | Enplas Corporation | Light scattering guiding light source device and liquid crystal display |
JP2003002937A (en) * | 2001-06-19 | 2003-01-08 | A & M Styrene Co Ltd | Molded product excellent in light transmission characteristics |
US6556347B1 (en) | 1998-12-18 | 2003-04-29 | Mitsubisi Rayon Co., Ltd. | Rear projection screen |
JP2006089596A (en) * | 2004-09-24 | 2006-04-06 | Sumitomo Dow Ltd | Polycarbonate resin composition for light diffusion plate and lighting cover composed of the same composition |
JP2006096937A (en) * | 2004-09-30 | 2006-04-13 | Sumitomo Chemical Co Ltd | Light-diffusing polycarbonate resin composition |
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US7960450B2 (en) | 2006-08-25 | 2011-06-14 | Styron Europe Gmbh | Flame retardant and light diffusing polycarbonate resin composition and light diffusing sheet thereof |
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JPS58173726A (en) * | 1982-04-05 | 1983-10-12 | Dainippon Printing Co Ltd | Lenticular sheet |
JPS5968333A (en) * | 1982-10-12 | 1984-04-18 | Toray Silicone Co Ltd | Spherical, cured polymer containing linear organopolysiloxane block or composition containing said polymer and production thereof |
JPS59179535A (en) * | 1983-03-29 | 1984-10-12 | Nitto Electric Ind Co Ltd | Method for forming metallized film giving irregular reflection |
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JPH0353059U (en) * | 1989-09-28 | 1991-05-22 | ||
JPH03167269A (en) * | 1989-11-27 | 1991-07-19 | Matsushita Electric Works Ltd | Milk-white coating composition |
JPH0573602U (en) * | 1991-10-09 | 1993-10-08 | 恵和商工株式会社 | Light diffusion sheet material |
JPH0573601U (en) * | 1991-10-09 | 1993-10-08 | 恵和商工株式会社 | Liquid crystal display |
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US6290364B1 (en) | 1993-04-05 | 2001-09-18 | Enplas Corporation | Surface light source device |
US5899552A (en) * | 1993-11-11 | 1999-05-04 | Enplas Corporation | Surface light source device |
US6152570A (en) * | 1993-11-11 | 2000-11-28 | Enplas Corporation | Surface light source device |
US6322225B1 (en) | 1993-12-17 | 2001-11-27 | Enplas Corporation | Light scattering guiding light source device and liquid crystal display |
JPH07216328A (en) * | 1994-02-04 | 1995-08-15 | Kimoto & Co Ltd | Light-diffusing pressure-sensitive adhesive composition |
JP2006154839A (en) * | 1994-05-18 | 2006-06-15 | Dainippon Printing Co Ltd | Antiglare film |
US6040044A (en) * | 1994-10-31 | 2000-03-21 | Dai Nippon Printing Co., Ltd. | Decorative material having abrasion resistance |
WO1996013381A1 (en) * | 1994-10-31 | 1996-05-09 | Dai Nippon Printing Co., Ltd. | Decorative material having abrasion resistance |
AU710878B2 (en) * | 1994-10-31 | 1999-09-30 | Dainippon Printing Co. Ltd. | Decorative material having abrasion resistance |
US5928778A (en) * | 1994-10-31 | 1999-07-27 | Dai Nippon Printing Co., Ltd. | Decorative material having abrasion resistance |
JPH11109112A (en) * | 1997-10-02 | 1999-04-23 | Nippon Synthetic Chem Ind Co Ltd:The | Manufacture of glare preventive treated layer |
JP2000098107A (en) * | 1998-09-24 | 2000-04-07 | Kimoto & Co Ltd | Forward scattering film |
US6556347B1 (en) | 1998-12-18 | 2003-04-29 | Mitsubisi Rayon Co., Ltd. | Rear projection screen |
US6760155B2 (en) | 1998-12-18 | 2004-07-06 | Mitsubishi Rayon Co., Ltd | Rear projection screen |
US7419715B2 (en) | 2000-07-18 | 2008-09-02 | Omron Corporation | Light diffusing films |
JP2003002937A (en) * | 2001-06-19 | 2003-01-08 | A & M Styrene Co Ltd | Molded product excellent in light transmission characteristics |
US7440049B2 (en) | 2004-02-09 | 2008-10-21 | Kuraray Co., Ltd. | Backlight device for liquid crystal display |
KR100783150B1 (en) * | 2004-02-09 | 2007-12-07 | 가부시키가이샤 구라레 | Backlight device for liquid crystal display |
JP2006089596A (en) * | 2004-09-24 | 2006-04-06 | Sumitomo Dow Ltd | Polycarbonate resin composition for light diffusion plate and lighting cover composed of the same composition |
JP2006096937A (en) * | 2004-09-30 | 2006-04-13 | Sumitomo Chemical Co Ltd | Light-diffusing polycarbonate resin composition |
WO2007049515A1 (en) | 2005-10-26 | 2007-05-03 | Asahi Kasei Chemicals Corporation | Light transmitting resin board |
WO2007063724A1 (en) | 2005-11-30 | 2007-06-07 | Mitsubishi Engineering-Plastics Corporation | Polycarbonate resin composition for light diffusion plate and light diffusion plate |
JPWO2008016088A1 (en) * | 2006-08-02 | 2009-12-24 | 旭硝子株式会社 | Light diffusion layer forming coating solution and light diffusion plate |
CN101495888A (en) * | 2006-08-02 | 2009-07-29 | 旭硝子株式会社 | Coating solution for forming light diffusion layer, and light diffusion plate |
WO2008016088A1 (en) * | 2006-08-02 | 2008-02-07 | Asahi Glass Company, Limited | Coating solution for forming light diffusion layer, and light diffusion plate |
JP5176958B2 (en) * | 2006-08-02 | 2013-04-03 | 旭硝子株式会社 | Light diffusion layer forming coating solution and light diffusion plate |
US7960450B2 (en) | 2006-08-25 | 2011-06-14 | Styron Europe Gmbh | Flame retardant and light diffusing polycarbonate resin composition and light diffusing sheet thereof |
US8426015B2 (en) | 2007-06-12 | 2013-04-23 | Styron Europe Gmbh | Clear and flame retardant polycarbonate resin film |
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JP2010531365A (en) * | 2007-06-28 | 2010-09-24 | 住友ダウ株式会社 | Light diffusing thermoplastic resin composition and light diffusing plate comprising the same |
KR20220093895A (en) | 2020-12-28 | 2022-07-05 | 주식회사 엘엑스엠엠에이 | A light diffusing bead, method of producing the same, and light diffusing sheets comprising thereof |
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