CN1993410A - Foamed sheet, and method and apparatus for producing same - Google Patents
Foamed sheet, and method and apparatus for producing same Download PDFInfo
- Publication number
- CN1993410A CN1993410A CNA2005800258633A CN200580025863A CN1993410A CN 1993410 A CN1993410 A CN 1993410A CN A2005800258633 A CNA2005800258633 A CN A2005800258633A CN 200580025863 A CN200580025863 A CN 200580025863A CN 1993410 A CN1993410 A CN 1993410A
- Authority
- CN
- China
- Prior art keywords
- plate
- foaming
- bubble
- thermoplastic resin
- gas
- 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
- 238000000034 method Methods 0.000 title claims description 33
- 238000004519 manufacturing process Methods 0.000 claims abstract description 32
- 229920005992 thermoplastic resin Polymers 0.000 claims abstract description 28
- 238000005187 foaming Methods 0.000 claims description 86
- 239000002023 wood Substances 0.000 claims description 24
- 239000006260 foam Substances 0.000 claims description 22
- 230000007246 mechanism Effects 0.000 claims description 19
- 238000005266 casting Methods 0.000 claims description 18
- 238000001125 extrusion Methods 0.000 claims description 15
- 238000012545 processing Methods 0.000 claims description 13
- 238000002310 reflectometry Methods 0.000 claims description 13
- 239000000463 material Substances 0.000 claims description 11
- 238000002834 transmittance Methods 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- 238000009434 installation Methods 0.000 claims description 9
- 239000000113 methacrylic resin Substances 0.000 claims description 8
- 229920000178 Acrylic resin Polymers 0.000 claims description 7
- 239000004925 Acrylic resin Substances 0.000 claims description 7
- 229910052751 metal Inorganic materials 0.000 claims description 7
- 239000002184 metal Substances 0.000 claims description 7
- 229920000642 polymer Polymers 0.000 claims description 7
- 239000000155 melt Substances 0.000 claims description 6
- 238000007789 sealing Methods 0.000 claims description 6
- 229910000831 Steel Inorganic materials 0.000 claims description 4
- 230000008676 import Effects 0.000 claims description 4
- 239000010959 steel Substances 0.000 claims description 4
- 230000028016 temperature homeostasis Effects 0.000 claims description 4
- 238000004049 embossing Methods 0.000 claims description 3
- 239000000835 fiber Substances 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- 238000005245 sintering Methods 0.000 claims description 2
- 239000007789 gas Substances 0.000 description 39
- 229920005989 resin Polymers 0.000 description 23
- 239000011347 resin Substances 0.000 description 23
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 12
- 235000011089 carbon dioxide Nutrition 0.000 description 12
- 229920000728 polyester Polymers 0.000 description 11
- 229960004424 carbon dioxide Drugs 0.000 description 10
- 239000004973 liquid crystal related substance Substances 0.000 description 10
- 239000000126 substance Substances 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 6
- 238000007493 shaping process Methods 0.000 description 6
- JHPBZFOKBAGZBL-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylprop-2-enoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)=C JHPBZFOKBAGZBL-UHFFFAOYSA-N 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
- -1 alkyl methacrylate Chemical compound 0.000 description 4
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 4
- 230000006835 compression Effects 0.000 description 4
- 238000007906 compression Methods 0.000 description 4
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- 239000000178 monomer Substances 0.000 description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 125000005250 alkyl acrylate group Chemical group 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 229920001225 polyester resin Polymers 0.000 description 3
- 239000004645 polyester resin Substances 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 230000006837 decompression Effects 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- 235000012204 lemonade/lime carbonate Nutrition 0.000 description 2
- 239000010445 mica Substances 0.000 description 2
- 229910052618 mica group Inorganic materials 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 238000012856 packing Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- UJTRCPVECIHPBG-UHFFFAOYSA-N 3-cyclohexylpyrrole-2,5-dione Chemical compound O=C1NC(=O)C(C2CCCCC2)=C1 UJTRCPVECIHPBG-UHFFFAOYSA-N 0.000 description 1
- IYMZEPRSPLASMS-UHFFFAOYSA-N 3-phenylpyrrole-2,5-dione Chemical compound O=C1NC(=O)C(C=2C=CC=CC=2)=C1 IYMZEPRSPLASMS-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 239000004727 Noryl Substances 0.000 description 1
- 229920001207 Noryl Polymers 0.000 description 1
- 239000004697 Polyetherimide Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004734 Polyphenylene sulfide Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- FMRLDPWIRHBCCC-UHFFFAOYSA-L Zinc carbonate Chemical compound [Zn+2].[O-]C([O-])=O FMRLDPWIRHBCCC-UHFFFAOYSA-L 0.000 description 1
- 239000005083 Zinc sulfide Substances 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- GHPGOEFPKIHBNM-UHFFFAOYSA-N antimony(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Sb+3].[Sb+3] GHPGOEFPKIHBNM-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- AOJOEFVRHOZDFN-UHFFFAOYSA-N benzyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC1=CC=CC=C1 AOJOEFVRHOZDFN-UHFFFAOYSA-N 0.000 description 1
- GCTPMLUUWLLESL-UHFFFAOYSA-N benzyl prop-2-enoate Chemical compound C=CC(=O)OCC1=CC=CC=C1 GCTPMLUUWLLESL-UHFFFAOYSA-N 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- FQEZLJDDYYNLPP-UHFFFAOYSA-N carbonic acid;tin Chemical compound [Sn].OC(O)=O FQEZLJDDYYNLPP-UHFFFAOYSA-N 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000013228 contact guidance Effects 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 238000003851 corona treatment Methods 0.000 description 1
- OIWOHHBRDFKZNC-UHFFFAOYSA-N cyclohexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1CCCCC1 OIWOHHBRDFKZNC-UHFFFAOYSA-N 0.000 description 1
- KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000000892 gravimetry Methods 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 230000001795 light effect Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 235000014380 magnesium carbonate Nutrition 0.000 description 1
- 229960001708 magnesium carbonate Drugs 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 235000012245 magnesium oxide Nutrition 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
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- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- QIWKUEJZZCOPFV-UHFFFAOYSA-N phenyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1=CC=CC=C1 QIWKUEJZZCOPFV-UHFFFAOYSA-N 0.000 description 1
- WRAQQYDMVSCOTE-UHFFFAOYSA-N phenyl prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1 WRAQQYDMVSCOTE-UHFFFAOYSA-N 0.000 description 1
- 230000000176 photostabilization Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
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- 229920003023 plastic Polymers 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 239000011120 plywood Substances 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
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- 229920006149 polyester-amide block copolymer Polymers 0.000 description 1
- 229920001601 polyetherimide Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 230000001568 sexual effect Effects 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229960001866 silicon dioxide Drugs 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 238000007666 vacuum forming Methods 0.000 description 1
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- 230000037303 wrinkles Effects 0.000 description 1
- 239000011667 zinc carbonate Substances 0.000 description 1
- 235000004416 zinc carbonate Nutrition 0.000 description 1
- 229910000010 zinc carbonate Inorganic materials 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C44/00—Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
- B29C44/34—Auxiliary operations
- B29C44/3442—Mixing, kneading or conveying the foamable material
- B29C44/3446—Feeding the blowing agent
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/22—After-treatment of expandable particles; Forming foamed products
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C44/00—Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/03—Extrusion 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
- B29C48/07—Flat, e.g. panels
- B29C48/08—Flat, e.g. panels flexible, e.g. films
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/16—Articles comprising two or more components, e.g. co-extruded layers
- B29C48/18—Articles comprising two or more components, e.g. co-extruded layers the components being layers
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
- C08J9/122—Hydrogen, oxygen, CO2, nitrogen or noble gases
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/16—Articles comprising two or more components, e.g. co-extruded layers
- B29C48/18—Articles comprising two or more components, e.g. co-extruded layers the components being layers
- B29C48/21—Articles comprising two or more components, e.g. co-extruded layers the components being layers the layers being joined at their surfaces
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/0079—Liquid crystals
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/04—Condition, form or state of moulded material or of the material to be shaped cellular or porous
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/25—Solid
- B29K2105/253—Preform
- B29K2105/256—Sheets, plates, blanks or films
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2995/00—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
- B29K2995/0012—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds having particular thermal properties
- B29K2995/0015—Insulating
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2995/00—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
- B29K2995/0012—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds having particular thermal properties
- B29K2995/0016—Non-flammable or resistant to heat
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2333/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
- C08J2333/04—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters
- C08J2333/06—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters of esters containing only carbon, hydrogen, and oxygen, the oxygen atom being present only as part of the carboxyl radical
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- Mechanical Engineering (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Extrusion Moulding Of Plastics Or The Like (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Optical Elements Other Than Lenses (AREA)
- Liquid Crystal (AREA)
- Laminated Bodies (AREA)
- Molding Of Porous Articles (AREA)
Abstract
Disclosed is an unstretched foamed sheet containing a thermoplastic resin. Not less than 80% of air bubbles contained in the sheet has a diameter of 0.1-20 mum, and the porosity of the foamed sheet is 20-80%. Also disclosed are a method for producing such a foamed sheet and an apparatus suitable for producing such a foamed sheet. Further disclosed are a light-reflecting plate using such a foamed sheet and a display.
Description
Technical field
The present invention relates to the plate that foams.The present invention relates to separator materials such as light reflecting board, battery, packing material, steel plate lamination in detail with material etc., particularly the foaming plate that can appropriately use with light reflecting board with the flat light source that uses in the backlight mechanism as display unit such as liquid crystal, be adapted at the device that uses in its manufacture method and its manufacturing installation and light reflecting board and the display unit of using this foaming plate.
Background technology
In recent years as the display equipment of the indicating meter of notebook computer or desktop computer, TV, portable phone etc., mostly use can slimming display unit such as liquid crystal.For example liquid crystal indicator is not owing to himself be twinkler, so be to be called the flat light source of backlight and just can to show from the rear side irradiates light by setting.This backlight normally takes to be called the flat light source structure of side lamp type or full run-down type for the uniform irradiation whole image.Particularly because notebook computer etc. is wished slim, miniaturization, so in the possible purposes of slim liquid-crystal display, side lamp type (being the form of irradiates light from the side for picture promptly) backlight is suitable for (with reference to patent documentation 1,2) usually.On the other hand, in the so big picture of LCD TV is used, because the side lamp mode can not reach high brightnessization, so be to adopt full run-down type lamp mode.
Usually under the situation of side lamp mode, cold cathode ray tube as light source, make light in the face of light guiding plate inside, evenly propagate, spread from the light guiding plate edge, and for handle reflects to the liquid crystal panel direction to the light with the diffusion of liquid crystal panel reverse direction expeditiously from light guiding plate, so below light guiding plate, be provided with reflector.And full run-down type lamp mode is to be set up in parallel cold cathode ray tube in the bottom of liquid crystal panel, cold cathode ray tube abreast and be listed on the reflector.As reflector can use plane or cold cathode ray tube partially-formed as the semicircle concavity etc.
As mentioned above, for the whole image of uniform irradiation liquid crystal indicator, the reflector role is big.Just require high reflection characteristic for the reflector that satisfies this effect, existing is that the thin slice etc. that the thin slice of micro bubble is contained in inside and added white pigment uses separately, or these sheet adherings in metal sheet, the first-class use of plastic plate.As the thin slice that this reflector uses, be to use the two spool extension white polyester sheet smaller mostly to reflected light directive property.Extending white polyester sheet in length and breadth is absorb fillers in resin, extends after being shaped by plate and forms fine voids.
But the existing main application of LCD device is a notebook computer, but adds in recent years in the various machines such as display equipment of desktop computer and TV, mobile phone etc. and be used and expansion to some extent.Just seeking to obtain the image of brighter distinctness, be used to realize that the improvement of high brightness, high degree of accuracy liquid crystal panel makes progress, also stricter for the desired characteristic of reflector.Therefore, be used for improving the discussion of extending the white polyester sheet reflection characteristic and carrying out (with reference to patent documentation 2,3) with keen determination.
But when the extension white polyester sheet is wanted to increase number of bubbles in order to improve reflection characteristic, just need in polyester, increase the use level of the resin and the particle of non-conforming.Therefore, this non-conforming resin and particle become the reason that reduces reflection characteristic on the contrary as light absorbing impurity, therefore, are difficult to wish to improve reflection characteristic.And,, consequently produce unfavorable phenomenons such as luminous reflectance factor reduction sometimes to specific wavelength so the size of bubble is roughly even owing to be by extending to form bubble.And under the situation of full run-down type lamp mode backlight, need carry out the shaping processing of waveform, but because the residual extensibility of the white polyester sheet that is extended is little, so be not suitable for this shaping processing to reflector.
As the substitute of above-mentioned extension white polyester sheet, that knows has: roller is remained in the pressurized inert gas, and after rare gas element being contained be dipped in the vibrin plate, heating makes foaming and the polyester resin foamed plate (with reference to patent documentation 4) that obtains under normal pressure.[title with MCPET (login trade mark) can obtain from The Furakawa Electric Co., Ltd.].
The polyester resin foamed plate that obtains by this method is owing to be to produce the mechanism of bubble when utilizing the pressure that discharges rare gas element, so contain impurity or bubble size is in full accord unlike the foaming that is obtained by extension.Consequently with extend white polyester sheet mutually specific energy improve reflection characteristic.And owing to be not to extend thin slice, the processing that is shaped is also easy.
Like this, above-mentioned polyester resin foamed plate has just been filled up the shortcoming of extending white polyester sheet.But owing to just need expend time in, so productivity is bad for rare gas element being contained be dipped in the vibrin plate.And because the plate surface is easy to generate brokenly bubble, so shaggy shortcoming is arranged.If further non-foam layer is set, then only after making the foaming of vibrin plate,, the shortcoming of bringing bad influence to reflection characteristic is arranged also then there not being the method that the foaming plate is pasted on the surface.
Know methyl methacrylate to be that polymer and whipping agent melt to mix by forcing machine and obtain foam cylindraceous in addition, then by extend, cooling, and cut and be distracted into tabular and manufacture method (with reference to the patent documentation 5) plate that obtains foaming.And know the micro bubble polymer materials of plate form is extruded and the method (with reference to patent documentation 6) of form layers compound product.But these methods so bubble size is big, can not fully improve reflection characteristic owing to can not control the size of bubble.
In the patent documentation 6 disclosed methods, foaming plate and the laminate that does not have a foaming plate be set by bonding carry out laminated.But bonding be laminated in the laminated border that has at the interface, thus reflection, refraction produced at the interface, even the absorption that also produces light, consider to have and bring the unfavorable condition of bad influence for easily whole reflection characteristic.
Also know the method (with reference to patent documentation 7~9) that makes gas the resin combination effect be obtained porous matter and even foaminess thin slice and plate in forcing machine is arranged.But in the patent documentation 7 disclosed methods, even the inert gas concentration in the polymkeric substance is suppressed low, bubble is not only big, nor can use in the light reflecting board of micro bubble.In the patent documentation 8 disclosed methods, in case also be to emit gas after forming plate, then the two sides gas concentration of plate has deviation, and the foaming part produces inhomogeneous with the partially mixed existence that does not have too foaming.Even in patent documentation 9 disclosed methods, considering has the unfavorable condition that bubble size becomes to grow up when extending.
Like this, although the control of the size of bubble or shape is not only extremely important in the foaming plate, and be difficult.
Patent documentation 1: the spy of Japan opens clear 63-62104 communique
Patent documentation 2: the spy of Japan opens the 2003-160682 communique
Patent documentation 3: the spy of Japan opens the 2001-305313 communique
Patent documentation 4: Japan speciallys permit communique No. 2713556
Patent documentation 5: the spy of Japan opens the 2000-86795 communique
Patent documentation 6: the special table 2001-510749 of Japan communique
Patent documentation 7: the spy of Japan opens the 2002-338726 communique
Patent documentation 8: the spy of Japan opens the 2000-119432 communique
Patent documentation 9: Japan speciallys permit communique No. 2902242
Therefore, just have and develop following problem, promptly, above-mentioned existing difficulty of extending the boundary of white polyester sheet reflection characteristic and the processing that is shaped in length and breadth, and then the size of bubble, shape appropriately changed according to purposes, productivity is good, and the surface is beautiful, as light reflecting board with suitable fine foaming plate.
Summary of the invention
Above-mentioned problem solves by the present invention of following record.
That is, the present invention contains thermoplastic resin and the nothing that constitutes is extended the foaming plate, have the bubble footpath of 0.1~20 mu m range in the bubble that relates in the plate being comprised more than 80%, and voidage is 20~80% foaming plate.
Other forms of the present invention relate to foam manufacture method of plate, it comprises: the melt polymer of the thermoplastic resin that has dissolved gas under acomia blister attitude, form plate operation, make the operation that produces bubble in a vacuum by under 50~200 ℃ temperature condition, plate being exposed.
Other forms again of the present invention relate to foam manufacture method of plate, it has dissolved the thermoplastic resin of gas and has not had the thermoplastic resin of gas dissolved to extrude together.
Other forms again of the present invention relate to foam manufacturing extrusion device of plate, it is the forcing machine that possesses screw rod, cylinder barrel and cylinder barrel thermoregulation mechanism, at a part of inner face of this cylinder barrel, possess and be used for the nozzle that imports from the high pressure gas feed unit gas supplied that is arranged on this cylinder barrel outside.
Other forms again of the present invention relate to foaming plate manufacturing installation, dispose: vacuum chamber device, and it possesses the chamber and the sealing mechanism that can reduce pressure inside at the casting roller of sheet forming machine and/or after casting roller; Vacuum generating device, it is attached to this vacuum chamber device.
Description of drawings
Fig. 1 is the diagrammatic illustration figure of expression the present invention embodiment plate with manufacturing installation;
Fig. 2 is the diagrammatic illustration figure in expression the present invention embodiment extrusion device nozzle segment longitudinal section;
Fig. 3 is that expression is the diagrammatic illustration figure of extrusion device nozzle segment shown in Figure 2 in the transverse section of A position cut-out.
Nomenclature
1 extrusion device, 1 1a extrusion device, 22 infeed means
3 molds, 4 casting rollers, 5 take off roll 1
5a take off roll 26 vacuum chambers 7 vacuum pumps
The cylinder body of 8 plates, 11 cylinder body 11a nozzle segments
12 screw rods, 13 well heaters, 14 jet elements
Embodiment
The result that the present inventor discusses has with keen determination found following content: the micro bubble that also has 0.1~20 mu m range when not having the extension cast panel, and the voidage of representing the gas phase occupation rate for certain above bubble density is in 20~80% scope, then as should obtaining beautiful, easy shaping processability in the unexistent surface of described existing foaming plate and good productivity at the foaming plate of use in the light reflecting board etc.
Foaming plate of the present invention is owing to be do not have to extend the foaming plate, so according to the purposes that is suitable for the foaming plate and the processing that is shaped easily.Extend in this said nothing and to be meant and not carry out, follow casting or form plate and the extension that produces degree and admit of so that plate produces single shaft or two extensions that are oriented to purpose and carry out.
Owing to foaming plate of the present invention, has the bubble footpath of 0.1~20 mu m range in the bubble that is comprised in the plate more than 80%, so can obtain good reflection characteristic.The bubble footpath that preferably has 0.4 μ m~8 mu m ranges in the bubble that is comprised in the plate more than 80%.Because the bubble footpath can cause interference of light effect etc. when too small, so can not obtain enough reflections.Opposite then need become big to the thickness of plate owing to have a certain amount of interface number when if the bubble footpath is excessive, consequently the physical strength of plate dies down, and needs than wishing design that film thickness is thick etc., is difficult to supply with practical.
In the existing extension board because bubble footpath evenly, so the unfavorable condition of the luminous reflectance factor reduction etc. of pair specific wavelength is arranged, but the bubble that foaming plate of the present invention is in the plate and is comprised is directly expressed proper distribution, and can obtain good reflection characteristic, and is favourable in this.
Foaming plate of the present invention is because voidage is in the scope that is 20~80%, so can obtain good reflection characteristic.Voidage is suitable with foaming bubble density that plate contained, expression be the gas phase occupation rate of plate, can ask it according to plate and the density of the resin that uses and the volume of plate.Preferably the voidage of plate is 50~70%.This is owing to be spherical shape in order to keep bubble shape, and theoretic maximum interspace rate is about 70%, if too surpass it, then bubble is destroyed and can not obtain the cause of good reflection characteristic.On the contrary, if voidage is low excessively, then the density of bubble is just low excessively, the reflection characteristic that can not obtain wishing.
When the reflector that uses in the backlight unit of foaming plate as full run-down type lamp mode is used, usually the foaming plate is applied the processing that is shaped with the forming temperature more than 100 ℃.Because this shaping handling ease and show good reflection characteristic, be more than 100% so foaming plate of the present invention is preferably in the extension elongation at failure that 100 ℃ environment measures down, and the extension stress under 100 ℃, 100% elongation is below the 50Mpa.Extending elongation at failure is to be ideal more than 150%, and extending stress is the following ideal of 0~30Mpa.
The main thermoplastic resin that formation the present invention foams plate in order to promote fine foaming, then preferably melts the high resin of tension force.Therefore, the melt flow dose rate (being as the criterion with ASTM D1238-98) of preferably representing the melted state flowability is 0.5~44g/10 minute a thermoplastic resin, and the flowability of melted state is that 1.4~30g/10 minute thermoplastic resin is better.The flowing property of thermoplastic resin is as the criterion and decides with the measuring condition of putting down in writing among the ASTM D1238-98 about various polymkeric substance (temperature, load).
Object lesson as the thermoplastic resin that can use in the present invention, can enumerate, for example, acrylic resin, methacrylic resin, polyolefine, polymeric amide, polyester, polycarbonate, styrene resin, polyethers, urethane, polyphenylene sulfide, polyesteramide, polyether ester, polyvinyl chloride, Noryl, polyarylester, polysulfones, polyimide, polyetherimide, polyamidoimide, be the multipolymer of main component and their mixture etc., but be not limited to these with them.
Particularly, owing to use acrylic resin and/or methacrylic resin when constituting the main thermoplastic resin of foaming sheet of the present invention, can obtain good especially fine foaminess, formability, so it is preferred, in addition, because the transparency height of resin itself, therefore final reflection at the bubble interface also becomes good.In addition, photostabilization is also excellent, and material resin can also obtain less expensively.
As the such acrylic resin or the object lesson of methacrylic resin, can enumerate, for example, the homopolymer of acrylate or methacrylic ester, the perhaps multipolymer of above acrylate of 50 weight % or methacrylic ester and other more than one vinyl monomers, wherein, the multipolymer of the methacrylic ester that preferred 50 weight % are above and more than one other vinyl monomers, the alkyl acrylate that alkyl methacrylate that especially preferred 50 weight % are above and 50 weight % are following, and 49 weight % following can with the multipolymer of more than one vinyl monomers of at least one copolymerization of alkyl methacrylate and alkyl acrylate.The preferred 0.1 weight % of the alkyl acrylate that contains in the multipolymer~40 weight % is more preferably 1 weight %~15 weight %.Aforesaid propylene acid resin or methacrylic resin can be used alone, but also also mix together respectively.
As such acrylate, can enumerate, for example, methyl acrylate, ethyl propenoate, butyl acrylate, cyclohexyl acrylate, phenyl acrylate, benzyl acrylate, 2-EHA, vinylformic acid 2-hydroxy methacrylate etc., preferred especially methyl acrylate, ethyl propenoate.In addition, as methacrylic ester, can enumerate, for example, methyl methacrylate, Jia Jibingxisuanyizhi, butyl methacrylate, cyclohexyl methacrylate, phenyl methacrylate, benzyl methacrylate, methacrylic acid 2-ethylhexyl, 2-hydroxyethyl methacrylate etc., special preferable methyl methyl acrylate, Jia Jibingxisuanyizhi.As other vinyl monomers that can copolymerization, except above-mentioned acrylate or methacrylic ester, can also enumerate, for example, unsaturated acids such as vinylformic acid, methacrylic acid, vinylbenzene, alpha-methyl styrene, vinyl cyanide, methacrylonitrile, maleic anhydride, phenyl maleimide, cyclohexyl maleimide etc.
The weight average molecular weight of aforesaid propylene acid resin or methacrylic resin (Mw) preferably 40,000~400,000, better is 60,000~300,000.If Mw is too small, and the physical strength of the foaming plate that then obtains is insufficient sometimes, and if Mw is excessive, and then melt viscosity uprises, and extrusion performance reduces sometimes.
Above-mentioned acrylic resin or methacrylic resin also can contain the rubber-like polymer.By the rubber-like polymer is cooperated to acrylic resin or methacrylic resin, can improve the viscosity and the toughness of resin, so can obtain the good foaming plate of shock-resistance.
Also can be in the scope of not damaging foaming plate reflection characteristic to thermoplastic resin of the present invention with a spot of, various additives below preferably 0~3% weight range cooperates, i.e. crystal nuclear agent, crystal promotor, the agent of bubble nuclear, antioxidant, stablizer, processing aids, plasticizer, charged preventor, shock-resistant auxiliary, whipping agent, weighting agent, matting agent, parting agent, fire retardant, UV light absorber, ultraviolet ray prevent agent, pigment, dyestuff, lubricant, white dyes etc.
The inorganic fine particles that works as the agent of bubble nuclear wherein, preferably can form the hole as nuclear, for example can use: lime carbonate, magnesiumcarbonate, zinc carbonate, titanium oxide (Detitanium-ore-type, rutile-type), zinc oxide, barium sulfate, zinc sulphide, alkaline carbonic acid tin, mica titanium, weisspiessglanz, magnesium oxide, calcium phosphate, silicon-dioxide, aluminum oxide, mica, talcum, kaolin etc. with himself.Wherein it is desirable to use visible region to absorb few lime carbonate, barium sulfate especially to 400~700nm.If there is absorption the visible region, then produce the problem that brightness reduces sometimes.
In order in plate, to form bubble, for example can enumerate carbonic acid gas, nitrogen, butane, helium, argon etc. as the gas that in forcing machine, is dissolved in the thermoplastic resin.Wherein carbonic acid gas, nitrogen low at gas permeation rate, cheap and can the point of safe handling on for well, also can be used alone or in combination them.
Foaming plate of the present invention is set the reflectivity of visible-range more than 85% for, and total light transmittance is set in below 10%, and this is beautiful as the surface, and the foaming plate that particularly suitable light reflecting board is used is an ideal.
Foaming plate of the present invention also can duplicate the embossing decorative pattern at least on single face.This embossing processing can be undertaken by following method, promptly by on the casting roller that is formed with fine decorative pattern from the teeth outwards decorative pattern after method that the thermoplastic resin plate duplicates or the casting roller by no decorative pattern are wound up into the foaming plate that has formed plate on the roller quickly, be re-applied to the method for on the calender device that the surface has fine decorative pattern decorative pattern being duplicated to plate.Can enumerate as fine decorative pattern and to be used to carry out wrinkle pattern, grid pattern, hemispherical pattern, chevron pattern, the pyramid shape pattern that the high-level efficiency luminous reflectance is used, or their Compound riffled etc.
Foam thickness 20~500 μ m preferably of plate of the present invention, 35~350 μ m are then better.Thickness then is difficult to guarantee the flatness of plate as if too small, is easy to generate bright inhomogeneous when using as light reflecting board.If thickness is excessive on the other hand, and then plasticity is bad sometimes.
Described foaming plate of the present invention, also can dispose one deck to it at least according to application target becomes two-layer above laminated wood.Set for when being laminated wood, preferably 1/200~1/3,1/50~1/4 better for the ratio of its secondary layer portion/main stor(e)y portion.Portion/main stor(e)y portion/when pair layer portion was three-layered lamination plate or the laminated wood more than three layers, this ratio was represented with the total/main stor(e)y portion of two secondary layer portion at secondary layer.Except above-mentioned foaming plate, also can dispose one deck non-foam layer at least in the laminated wood.Foaming plate of the present invention preferably is configured in the laminated wood as above-mentioned main stor(e)y portion.
Laminated wood of the present invention also can be by coextrusion, extrude stacked, heat lamination, coating, evaporation waits and forms.Particularly the laminated wood of coextrusion is best.This laminated wood for example can by from foaming layer with main extruder and non-foam layer with the polymkeric substance of secondary forcing machine in mold mouth mould manifold portion or the feeding portion that is arranged on before entering mould converges formation.This coextrusion laminated wood is not owing to need to be provided with bond layer, so favourable for reflection characteristic, productivity is also good simultaneously.Better is for example can make in the foaming part and not have foaming by setting for the main raw material of main extruding layer and secondary extruding layer composition identical partly not have border etc. in the place, can reduce the influence of main stor(e)y and secondary layer boundary surface, can be favourable when particularly using as light reflecting board.
This coextrusion laminated wood can not only be the double-layer structure of main stor(e)y (A layer) and secondary layer (B layer), and can also be the three-decker of (B layer) (A layer) (B layer), and then can be to have (B layer) (A layer) (B layer) (A layer) ... the multilayered structure of (B layer) (A layer) (B layer), very effective on the point of the easy control thickness direction bubble formation state of energy.
Other forms of the present invention relate to foam manufacturing extrusion device of plate, it is the forcing machine that possesses screw rod, cylinder barrel and cylinder barrel thermoregulation mechanism, at a part of inner face of this cylinder barrel, possess and be used for the nozzle that imports from the high pressure gas feed unit gas supplied that is arranged on this cylinder barrel outside.This extrusion device is fit to the manufacturing of above-mentioned foaming plate of the present invention or laminated wood.At this, said high pressure is the pressure of postcritical state preferably, for example be to the situation of extruding the favourable carbonic anhydride of gas foaming under, stagnation point is 31.3 ℃ of temperature, 7.52Mpa firmly.Therefore, the high pressure gas feed unit preferably can be all gases to surpass the device that the state of stagnation point is separately supplied with.
The extrusion device that the present invention can use also can be any of series connection forcing machine of series connection forcing machine, combination biaxial extruder and the single shaft forcing machine of single shaft forcing machine, biaxial extruder, binding single shaft forcing machine.The cylinder barrel of forcing machine partly possesses: the well heater that is used to heat, comprise the register that is used for refrigerative air cooling device, water cooling plant or oil cooling device, they preferably can be divided into 5~10 sections and control.Cylinder barrel preferably can be distinguished with the temperature adjustment control section and in the same manner by sectionization.Screw rod mainly is divided into district, the district of fusing press resin, the compression district of mixing of feeding material resin usually.The size of screw rod etc. can be carried out optimum design according to employed resin.
The inside of described extrusion device is provided with and is used for making the nozzle of gas dissolving in the resin that has melted in forcing machine, preferably is configured in the fusing compression zone of screw size.Be exactly specifically, this nozzle is set in place on the inner face of the cylinder barrel one section part of fusing compression zone, is used for importing from being arranged on outside high pressure gas feed unit gas supplied.
Its shape of nozzle preferably spreads all over the minute aperture in full week on the inner face of cylinder barrel one section part, for example be to have following, the structure of voidage below 25% of bubble footpath 30 μ m, be exactly that the nozzle that can load and unload the ring-type of metal or pottery formation is installed on the cylinder barrel inner face specifically.This annular metal preferably is made of the material of sintering metal powder or steel fiber.
Other forms again of the present invention relate to foaming plate manufacturing installation, dispose: vacuum chamber device, and it possesses the chamber and the sealing mechanism that can reduce pressure inside at the casting roller of sheet forming machine and/or after casting roller; Vacuum generating device, it is attached to this vacuum chamber device.This manufacturing installation is fit to the manufacturing of above-mentioned foaming plate of the present invention or laminated wood.
The foaming plate of this vacuum chamber device in order to obtain wishing preferably can reduce pressure the chamber interior that can reduce pressure to below the 30Mpa.
The sheet forming machine that the present invention can use generally includes: be used for molten resin forcing machine, be used to form plate flat-die, be used for the casting roller of cooling plate, the towing mechanism and the wind2 of plate.Flat-die is T shape mould preferably, can enumerate: possess stacked infeed mean device in the branch manifold type of mould inner laminated with in front of mould.The casting roller possesses temperature adjustment function usually, and method for regulating temperature makes water coolant, warm water or wet goods carry out round-robin, also has further to make up with induction heating mode.The plate towing mechanism also can then be cast the temperature adjustment function that roller has roller, also can possess: apparatus for measuring thickness, shortcoming proofing unit, prevent surface processing devices such as Charging system, corona treatment and framework processing.Wind2 also can possess: swiveling head mechanism, touch roll mechanism, change of lap mechanism, tenslator etc.
The chamber device that the present invention can use is to be positioned at casting roller or the top that then casts the towing mechanism central roll of roller, has along the section of the curvature of roller, and meets the case shape device of plate width, can discharge the air of chamber interior by the vacuum pump of outer setting and reduce pressure.Chamber has the sealing mechanism that is used to keep vacuum, is made of a plurality of spaces as required.
The sealing mechanism of the subsidiary chamber device that the present invention can use comprises: for the moving direction of plate current be inlet seal, the outlet of inlet side exit seal, be configured in the side seal of both sides, can adopt labyrinth seal type, contact roller mode closed type etc. for inlet seal and exit seal.Can adopt labyrinth seal type, contact guidance type etc. as side seal.
About the foam manufacture method of plate of the present invention, at its concrete example of following explanation, but the present invention is not limited to these concrete examples.
At first as required the moldable resin sheet that becomes heating and/or dry raw material heat, respectively to preheated can foam main extruder of extruding (A) and the secondary forcing machine (B) that foams supply.Main extruder (A) is by being positioned at the outer gas supply device of machine preferably with the condition supply gas more than the super critical condition.In main extruder (A) inside, the thermoplastic resin and the gas that have melted are fully mixed, and make gas dissolving in thermoplastic resin and be extruded.
The polymkeric substance of extruding the polymkeric substance of extruding from main extruder (A) (a) with from secondary forcing machine (B) (b) merges into (b) (a) after (b) three layers by infeed mean, supplies with to T shape mould, and becomes tabular and spue.At this moment adjust gas delivery volume so that polymkeric substance (a) becomes and is dissolved with gas and is the nothing foaming board status that does not have foaming.
The plate land that spue from T shape mould are cooled off at the casting roller.At this moment the plate uniform plate of vitreous state normally.After the temperature that is cooled to stipulate on the casting roller, plate is imported to the take off roll of then casting roller.By the vacuum chamber that is arranged on the take off roll plate is exposed under the vacuum state then.Like this, plate is varied to the plate of ultrawhite look with regard to producing fine foaming.Afterwards by up-coiler this coiled sheet on roller.
Described foaming plate of the present invention or laminated wood can be made by comprising the method that the thermoplastic resin that has dissolved gas is extruded the operation that makes foaming.At this moment, also can not use vacuum chamber device to foam, also can make the plate of acomia blister attitude or foamed state pass through vacuum chamber device.
Certain form of the present invention relate to foam manufacture method of plate, it comprises: the melt polymer of the thermoplastic resin that has dissolved gas under acomia blister attitude, form plate operation, make the operation that produces bubble in a vacuum by under 50~200 ℃ temperature condition, plate being exposed.This manufacture method is fit to the manufacturing of above-mentioned foaming plate of the present invention or laminated wood, and above-mentioned each operation is successive preferably.At this, temperature condition it would be desirable 70~120 ℃.
" forming plate with acomia blister attitude " among the present invention, is to make gas dissolving in the molten resin polymkeric substance, and forms plate with acomia blister attitude when partly being spued by mold, can carry out by the amount and/or the control condition of spuing that reduce gas dissolved.The plate of blister attitude that this is acomia is owing to having gas dissolving in the polymkeric substance, so by just making foaming easily to stimulations such as plate reduce pressure.
Form foaming method behind plate according to this, the condition of temperature by adjusting plate or decompression etc. just can be controlled the generation state of bubble easily, therefore, makes optimized some coideal of bubble size and number of bubbles easily.
The foaming plate is to have dissolved the thermoplastic resin of gas and do not had the thermoplastic resin of gas dissolved to extrude the manufacturing gained together by handle in certain form of the present invention.This manufacture method is fit to the manufacturing of above-mentioned foaming plate of the present invention or laminated wood.
Like this, foaming plate of the present invention can obtain by using then gas to supply with formation panel assembly and the vacuum chamber device extruded.Therefore, on streamline, can productivity make reflection characteristic, processibility, the good plate of surface smoothing well.
Described foaming plate of the present invention or laminated wood can use rightly as light reflecting board.This light reflecting board also can have been implemented the processing that is shaped to described foaming plate or laminated wood.
Shaping processing of the present invention is meant the mould of use energy attemperation, by carrying out vacuum forming, pressing empty shaping or drawing or rolling press processing etc. to obtain molding.
Embodiment
Followingly describe the present invention in detail, but the present invention is not limited to this embodiment according to embodiment.
[evaluation method]
1, reflectivity
Reflectivity is in spectrophotometer U-3410[(strain) Hitachi's system] go up to continue to get φ 60 integrating sphere 130-0632[(strains) Hitachi's system] and the state of 10 ℃ of inclination liners, for the two sides of foaming plate or laminated wood obtain visible-range (380~780nm) reflectivity, high value as reflectivity.
2, voidage
Voidage is the ratio of the relative resin board volume of bubble volume, is the volume of obtaining sample according to the thickness and the area of plate, and gravimetry uses following formula as voidage.
Voidage (%)=[1-(weight/resin density)/volume] * 100
3, plate thickness
Thickness measurement about foaming plate or laminated wood, be on the width of foaming plate or laminated wood, 10 measuring points to be set equally spaced, after used thickness meter (teclock society system thickness gauge) has been measured the thickness of measuring point, the average thickness of each point measured value as the foaming plate.
4, total light transmittance
Total light transmittance is as the criterion with JIS K7150:1981 and estimates foaming plate or laminated wood.
5, extend elongation at failure
Extend elongation at failure and be to use (strain) Ou Lienteke (オ リ エ Application テ Star Network) system day western sieve (テ Application シ ロ Application) UCT-100 elongation test machine, the plate of width 10mm, length 100mm after keeping 5 minutes under 100 ℃ the environment, when making elongation with 300mm/ minute, the mean value of elongation at failure on plate length direction and the transverse direction.
6, extend stress
Extend stress and be to use (strain) Ou Lienteke (オ リ エ Application テ Star Network) system day western sieve (テ Application シ ロ Application) UCT-100 elongation test machine, the plate of width 10mm, length 100mm after keeping 5 minutes under 100 ℃ the environment, when making elongation with 300mm/ minute, the mean value of the stress value of 100% elongation moment point of plate length direction and transverse direction.
[embodiment 1]
Under the condition of 120 ℃ of preheatings, optics is heated four hours as raw material with acrylic resin [this close peck of Sumitomo Chemical (strain) is thought (ス ミ ペ Star Network ス) MGSS], is it that 34 single shaft forcing machine, second section 50mm, L/D are that the series connection forcing machine of 28 single shaft forcing machine is supplied with to first section 35mm, L/D, and the high pressure gas feedway outside being arranged on the forcing machine machine is to cross 38 ℃, 15Mpa of super critical condition, the nozzle of carbonic anhydride on the bore section that is arranged on first section forcing machine fusing compression unit supplied with, made in resin dissolving and mix.At this moment the feed rate of carbonic anhydride is the discharge-amount 14.7kg/h of relative forcing machine and the ratio of carbonic anhydride is set for 0.38kg/h.At this moment be that extrusion temperature is 240 ℃ at first section, is 200 ℃ at second section.
It is spued and the result that forms plate is to have obtained the white foaming plate of mean thickness 230 μ m, width 88mm from the mould of slit width 150mm, interval of slit 0.8mm.
With slicing machine the thin slice section is not cut off with destroying, use the section that cuts off scanning electron microscope S-2100A type [(strain) Hitachi system] to observe with 500 times, the result is that the center in bubble footpath is 14 μ m, the bubble footpath that has the following scope of 20 μ m more than 80% of bubble.The voidage of bubble is 76% according to density calculation.
The result who shaggy part is removed the reflectivity of back this plate visible-range of mensuration is 85%, and total light transmittance is 6%.
Use the strong elongation apparatus for automatically measuring of thin slice [Ou Lienteke (オ リ エ Application テ Star Network) system day western sieve (テ Application シ ロ Application) AMF/RTA-100], with test portion dimension width 10mm * test portion length at interval 100mm, 100 ℃ of temperature, extension speed 200mm/ minute condition measure, the result is that to extend elongation at failure be 141%, is 12.0Mpa at 100 ℃, extension stress during 100% elongation.For the purpose of prudent, implemented simple and easy forming test, the result is that plasticity is good.
[embodiment 2]
Except the discharge-amount of forcing machine being set for 14.3kg/h, carbonic anhydride is supplied with the ratio of 0.03kg/h, carry out similarly to Example 1, the result who has formed plate has obtained transparent level and smooth plate.On one side this plate is heated to 90 ℃, is, foam and bleach turbid Yi Bian put the result of the 28kPa that reduces pressure in the moisture eliminator (vacuum chamber) into.
The white plate that obtains (mean thickness 205 μ m) is observed with method similarly to Example 1, and the result is that the center in bubble footpath is 10 μ m, the bubble footpath that has the following scope of 20 μ m more than 85% of bubble.And voidage is 56%.The reflectivity of this plate visible-range is 88%, and total light transmittance is 7%.Some is coarse a little for condition of surface, but it is low to be unlikely to reflectivity.
Extension elongation at failure under 100 ℃ is 195%, is 12.5Mpa at 100 ℃, extension stress during 100% elongation.
[embodiment 3]
The transparent panel that obtains with similarly to Example 2 method is heated to 50 ℃ on one side, Yi Bian put the 28kPa that reduces pressure in the moisture eliminator into.
The bubble size of the foaming plate that consequently obtains diminishes, and the center in bubble footpath is 7 μ m, and 100% of bubble has the bubble footpath of the following scope of 20 μ m.And voidage is 32%.The reflectivity of this plate visible-range is 89%, and total light transmittance is 10%.Condition of surface is no problem.
[embodiment 4]
Be that the transparent panel that obtains with similarly to Example 2 method is heated to 140 ℃ on one side specifically, Yi Bian put the 28kPa that reduces pressure in the moisture eliminator into.
It is big that the bubble size of the foaming plate that consequently obtains becomes, and deviation becomes big.The center in bubble footpath is 18 μ m, and 80% of bubble has the bubble footpath of the following scope of 20 μ m.And voidage is 61%.The reflectivity of this plate visible-range is 86%, and total light transmittance is 9%.The surface has the vestige of broken bubble everywhere.
[embodiment 5]
Use main extruder to carry out two sections and extrude (A layer) with similarly to Example 1 material, device, operating condition, also have that to be to use 45mm, L/D as secondary forcing machine be 34 single shaft forcing machine, supply with carbonic anhydride to the resin identical [this close peck of Sumitomo Chemical (strain) is thought (ス ミ ペ Star Network ス) MGSS] with main extruder, and extrude (B layer), utilization is arranged on infeed mean in front of the mould, and the three-decker of laminated one-tenth (B layer)/(A layer)/(B layer) forms plate similarly to Example 2 by both are carried out coextrusion.And in moisture eliminator, be exposed in the decompression similarly to Example 2, make foaming.
(mean thickness 245 μ m) are different with embodiment 2 for the white layer plywood that obtains, and the surface is level and smooth in the extreme.Observe with method similarly to Example 1, the result is that the center in bubble footpath is 8 μ m, and 90% of bubble has the bubble footpath of the following scope of 20 μ m.And voidage is 50%.The reflectivity of this plate visible-range is 89%, and total light transmittance is 9%.
Extension elongation at failure under 100 ℃ is 163%, is 13.3Mpa at 100 ℃, extension stress during 100% elongation.
[comparative example 1]
Except the carbonic anhydride increment to 0.6kg/h, carry out similarly to Example 1, carried out forming plate and the foaming plate that obtains white.But will behind mould, constantly break bubble, produce plosive.Fluctuation is seen on surface at plate, and voidage also is increased to 85%.
[comparative example 2]
Except the carbonic anhydride decrement to 0.1kg/h, carry out similarly to Example 1, carried out the formation plate and obtained translucent plate.Bubble directly is distributed in the scope of 20~100 μ m, and particularly the above big bubble of 50 μ m accounts for more than 50%.
[comparative example 3]
Except further the carbonic anhydride decrement to 0.05kg/h, carry out similarly to Example 1, carried out forming plate and obtained roughly transparent plate.But there is the above big bubble of 2mm irregularly to occur everywhere.
[comparative example 4]
Except not supplying with the carbonic anhydride, carry out similarly to Example 1, carry out forming plate and obtained transparent plate.This plate is reduced pressure in moisture eliminator similarly to Example 2, but do not see bubble generation.
[comparative example 5]
The transparent plate that do not foam that embodiment 2 obtains is put in the moisture eliminator and reduced pressure while being heated to 40 ℃, but do not see bubble generation.
[comparative example 6]
The transparent plate that do not foam that embodiment 2 obtains is put in the moisture eliminator and reduced pressure while being heated to 210 ℃, and the result is that there is the such foaming of balloon on the surface everywhere.
[comparative example 7]
The transparent plate that do not foam that embodiment 2 is obtained is heated on one side 90 ℃ of one side similarly to Example 2 and puts in the moisture eliminator and reduce pressure, and places one hour under this state.The plate that the plate that obtains obtains than embodiment 2, bubble growth big, the center in bubble footpath is 30 μ m, 60% of bubble has the bubble footpath of the following scope of 20 μ m.The reflectivity of this plate visible-range is 75%, and total light transmittance is 6%.
Foaming buttress of the present invention can be useful in reflector, packing material, steel plate lamination with in material, the separator material etc. according to its white, adverse environment resistant, heat retaining property, insulativity, micro bubble contain sexual, but its scope of application is not limited thereto.Foaming plate of the present invention can use especially rightly as the employed flat light source light reflecting board of the backlight mechanism of liquid crystal indicator.
Claims (23)
1, a kind of foaming plate, it is that the nothing that contains thermoplastic resin is extended the foaming plate, have the bubble footpath of 0.1~20 mu m range in the bubble that is comprised in the plate more than 80%, and voidage is 20~80%.
2, foaming plate as claimed in claim 1, wherein, the extension elongation at failure of measuring under 100 ℃ environment is more than 100%, and is below the 50Mpa at 100 ℃, the extension stress of 100% elongation.
3, foaming plate as claimed in claim 1 or 2, wherein, the melted state flowability of thermoplastic resin (being as the criterion with ASTM D1238-98) is 0.5~44g/10 minute.
4, as each described foaming plate of claim 1~3, wherein, thermoplastic resin is acrylic resin and/or is methacrylic resin.
5, as each described foaming plate of claim 1~4, wherein, contain the nuclear agent of 0~3% weight.
6, as each described foaming plate of claim 1~5, wherein, on single face, duplicated embossing at least.
7, a kind of laminated wood is two-layer above laminated wood, and it disposes each described foaming plate of one deck such as claim 1~6 at least.
8, laminated wood as claimed in claim 7, it disposes one deck non-foam layer at least.
9, as each described plate of claim 1~8, wherein, the reflectivity of visible-range is more than 85%, and total light transmittance is below 10%.
10, a kind of light reflecting board, wherein, it has used each described plate of claim 1~9.
11, a kind of light reflecting board, wherein, it is to the described firm and hard processing that is shaped of having executed of claim 10.
12, a kind of display unit, wherein, it has used claim 10 or 11 described light reflecting boards.
13, the manufacture method of the described plate of a kind of claim 1~9, wherein, it comprises having dissolved the thermoplastic resin of gas by extruding the operation that makes foaming.
14, a kind of manufacture method of the plate that foams, wherein, it comprises:
The melt polymer of the thermoplastic resin that has dissolved gas under acomia blister attitude, form plate operation,
By under 50~200 ℃ temperature condition, plate being exposed the operation that makes the generation bubble in a vacuum.
15, a kind of manufacture method of each described plate of claim 1~9, wherein, it comprises:
The melt polymer of the thermoplastic resin that has dissolved gas under acomia blister attitude, form plate operation,
By under 50~200 ℃ temperature condition, plate being exposed the operation that makes the generation bubble in a vacuum.
16, as the manufacture method of claim 1~9,13~15 each described plates, wherein, it has dissolved the thermoplastic resin of gas and has not had the thermoplastic resin of gas dissolved to extrude together.
17, a kind of foaming plate manufacturing extrusion device, it is the forcing machine that possesses screw rod, cylinder barrel and cylinder barrel thermoregulation mechanism, it is characterized in that, possessing and be used for the nozzle that imports from the high pressure gas feed unit gas supplied that is arranged on this cylinder barrel outside at the inner face of the part of this cylinder barrel.
18, each described plate manufacturing extrusion device of a kind of claim 1~9, it is the forcing machine that possesses screw rod, cylinder barrel and cylinder barrel thermoregulation mechanism, it is characterized in that, at the inner face of the part of this cylinder barrel, possess and be used for the nozzle that imports from the high pressure gas feed unit gas supplied that is arranged on this cylinder barrel outside.
19, as claim 17 or 18 described extrusion devices, wherein, described nozzle is made of annular metal with minute aperture or pottery.
20, extrusion device as claimed in claim 19, wherein, described annular metal is made of the material of sintering metal powder or steel fiber.
21, a kind of foaming plate manufacturing installation, wherein, it disposes: vacuum chamber device, it possesses the chamber and the sealing mechanism that can reduce pressure inside after the casting roller of sheet forming machine and/or casting roller; Vacuum generating device, it is attached to this vacuum chamber device.
22, each described plate manufacturing installation of a kind of claim 1~9, wherein, it disposes: vacuum chamber device, it possesses the chamber and the sealing mechanism that can reduce pressure inside after the casting roller of sheet forming machine and/or casting roller; Vacuum generating device, it is attached to this vacuum chamber device.
23, as claim 21 or 22 described manufacturing installations, wherein, described vacuum chamber device can reduce pressure the chamber interior that can reduce pressure to below the 30Kpa.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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JP224156/2004 | 2004-07-30 | ||
JP2004224156A JP4093419B2 (en) | 2004-07-30 | 2004-07-30 | Foam sheet, manufacturing method and manufacturing apparatus thereof |
PCT/JP2005/013750 WO2006011521A1 (en) | 2004-07-30 | 2005-07-27 | Foamed sheet, and method and apparatus for producing same |
Publications (2)
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CN1993410A true CN1993410A (en) | 2007-07-04 |
CN1993410B CN1993410B (en) | 2012-05-30 |
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CN2005800258633A Expired - Fee Related CN1993410B (en) | 2004-07-30 | 2005-07-27 | Foamed sheet, and method and apparatus for producing same |
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JP (1) | JP4093419B2 (en) |
KR (1) | KR100842524B1 (en) |
CN (1) | CN1993410B (en) |
TW (1) | TWI347334B (en) |
WO (1) | WO2006011521A1 (en) |
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- 2005-07-27 WO PCT/JP2005/013750 patent/WO2006011521A1/en active Application Filing
- 2005-07-27 KR KR1020077002313A patent/KR100842524B1/en not_active IP Right Cessation
- 2005-07-27 CN CN2005800258633A patent/CN1993410B/en not_active Expired - Fee Related
- 2005-07-29 TW TW094125725A patent/TWI347334B/en not_active IP Right Cessation
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Also Published As
Publication number | Publication date |
---|---|
WO2006011521A1 (en) | 2006-02-02 |
KR100842524B1 (en) | 2008-07-01 |
TWI347334B (en) | 2011-08-21 |
TW200615317A (en) | 2006-05-16 |
CN1993410B (en) | 2012-05-30 |
JP2006045259A (en) | 2006-02-16 |
KR20070039106A (en) | 2007-04-11 |
JP4093419B2 (en) | 2008-06-04 |
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