JP2002542087A - Ｕｖ安定化ポリマー構造物 - Google Patents
Ｕｖ安定化ポリマー構造物Info
- Publication number
- JP2002542087A JP2002542087A JP2000613645A JP2000613645A JP2002542087A JP 2002542087 A JP2002542087 A JP 2002542087A JP 2000613645 A JP2000613645 A JP 2000613645A JP 2000613645 A JP2000613645 A JP 2000613645A JP 2002542087 A JP2002542087 A JP 2002542087A
- Authority
- JP
- Japan
- Prior art keywords
- group
- cyclobutanediol
- polycarbonate
- tetramethyl
- structure according
- 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.)
- Pending
Links
- 229920000642 polymer Polymers 0.000 title claims description 40
- 229920000515 polycarbonate Polymers 0.000 claims abstract description 61
- 239000004417 polycarbonate Substances 0.000 claims abstract description 61
- 150000001875 compounds Chemical class 0.000 claims abstract description 48
- FQXGHZNSUOHCLO-UHFFFAOYSA-N 2,2,4,4-tetramethyl-1,3-cyclobutanediol Chemical compound CC1(C)C(O)C(C)(C)C1O FQXGHZNSUOHCLO-UHFFFAOYSA-N 0.000 claims abstract description 23
- 230000006750 UV protection Effects 0.000 claims abstract description 21
- 239000012964 benzotriazole Substances 0.000 claims abstract description 19
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 claims abstract description 16
- HQQTZCPKNZVLFF-UHFFFAOYSA-N 4h-1,2-benzoxazin-3-one Chemical compound C1=CC=C2ONC(=O)CC2=C1 HQQTZCPKNZVLFF-UHFFFAOYSA-N 0.000 claims abstract description 15
- 230000005855 radiation Effects 0.000 claims abstract description 15
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000010410 layer Substances 0.000 claims description 59
- 229920000728 polyester Polymers 0.000 claims description 26
- 239000011241 protective layer Substances 0.000 claims description 23
- 125000000217 alkyl group Chemical group 0.000 claims description 21
- 125000003118 aryl group Chemical group 0.000 claims description 20
- 239000000463 material Substances 0.000 claims description 18
- 125000004432 carbon atom Chemical group C* 0.000 claims description 13
- 229920001577 copolymer Polymers 0.000 claims description 13
- 150000002334 glycols Chemical class 0.000 claims description 13
- -1 benzotriazole compound Chemical class 0.000 claims description 12
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 10
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 9
- 239000004800 polyvinyl chloride Substances 0.000 claims description 8
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 7
- 239000000126 substance Substances 0.000 claims description 7
- 239000004801 Chlorinated PVC Substances 0.000 claims description 6
- 239000004952 Polyamide Substances 0.000 claims description 6
- 239000004695 Polyether sulfone Substances 0.000 claims description 6
- 239000004697 Polyetherimide Substances 0.000 claims description 6
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 6
- 229920000457 chlorinated polyvinyl chloride Polymers 0.000 claims description 6
- 229920002647 polyamide Polymers 0.000 claims description 6
- 229920006393 polyether sulfone Polymers 0.000 claims description 6
- 150000001565 benzotriazoles Chemical class 0.000 claims description 5
- 150000002009 diols Chemical class 0.000 claims description 5
- 125000000524 functional group Chemical group 0.000 claims description 5
- 150000002148 esters Chemical class 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 229920006162 poly(etherimide sulfone) Polymers 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 125000005586 carbonic acid group Chemical group 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 3
- 150000003918 triazines Chemical class 0.000 claims description 3
- 229920002943 EPDM rubber Polymers 0.000 claims description 2
- 229920000181 Ethylene propylene rubber Polymers 0.000 claims description 2
- 239000004677 Nylon Substances 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000004104 aryloxy group Chemical group 0.000 claims description 2
- 125000004185 ester group Chemical group 0.000 claims description 2
- 125000001072 heteroaryl group Chemical group 0.000 claims description 2
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 229920001778 nylon Polymers 0.000 claims description 2
- 229920001601 polyetherimide Polymers 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims 2
- 150000002431 hydrogen Chemical class 0.000 claims 2
- MHPMXFUDCYMCOE-UHFFFAOYSA-N cyclobutane-1,2-diol Chemical compound OC1CCC1O MHPMXFUDCYMCOE-UHFFFAOYSA-N 0.000 claims 1
- XKZQKPRCPNGNFR-UHFFFAOYSA-N 2-(3-hydroxyphenyl)phenol Chemical compound OC1=CC=CC(C=2C(=CC=CC=2)O)=C1 XKZQKPRCPNGNFR-UHFFFAOYSA-N 0.000 abstract description 4
- 229920001651 Cyanoacrylate Polymers 0.000 abstract description 3
- MWCLLHOVUTZFKS-UHFFFAOYSA-N Methyl cyanoacrylate Chemical compound COC(=O)C(=C)C#N MWCLLHOVUTZFKS-UHFFFAOYSA-N 0.000 abstract description 3
- 238000000034 method Methods 0.000 description 11
- 239000000203 mixture Substances 0.000 description 11
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 9
- 229920001634 Copolyester Polymers 0.000 description 8
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 6
- 238000001125 extrusion Methods 0.000 description 6
- 239000010408 film Substances 0.000 description 6
- 230000000087 stabilizing effect Effects 0.000 description 6
- 238000004383 yellowing Methods 0.000 description 6
- 239000011159 matrix material Substances 0.000 description 5
- 239000002861 polymer material Substances 0.000 description 5
- 229920000402 bisphenol A polycarbonate polymer Polymers 0.000 description 4
- 230000015556 catabolic process Effects 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 238000010276 construction Methods 0.000 description 4
- 238000006731 degradation reaction Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 description 4
- 239000005020 polyethylene terephthalate Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- STENYDAIMALDKF-UHFFFAOYSA-N cyclobutane-1,3-diol Chemical compound OC1CC(O)C1 STENYDAIMALDKF-UHFFFAOYSA-N 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000003475 lamination Methods 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 230000007812 deficiency Effects 0.000 description 2
- 239000000539 dimer Substances 0.000 description 2
- 238000005562 fading Methods 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 1
- GETTZEONDQJALK-UHFFFAOYSA-N (trifluoromethyl)benzene Chemical compound FC(F)(F)C1=CC=CC=C1 GETTZEONDQJALK-UHFFFAOYSA-N 0.000 description 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- PXGZQGDTEZPERC-UHFFFAOYSA-N 1,4-cyclohexanedicarboxylic acid Chemical compound OC(=O)C1CCC(C(O)=O)CC1 PXGZQGDTEZPERC-UHFFFAOYSA-N 0.000 description 1
- VSXIZXFGQGKZQG-UHFFFAOYSA-N 2-cyano-3,3-diphenylprop-2-enoic acid Chemical class C=1C=CC=CC=1C(=C(C#N)C(=O)O)C1=CC=CC=C1 VSXIZXFGQGKZQG-UHFFFAOYSA-N 0.000 description 1
- VEORPZCZECFIRK-UHFFFAOYSA-N 3,3',5,5'-tetrabromobisphenol A Chemical compound C=1C(Br)=C(O)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(O)C(Br)=C1 VEORPZCZECFIRK-UHFFFAOYSA-N 0.000 description 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000012963 UV stabilizer Substances 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000008033 biological extinction Effects 0.000 description 1
- FQUNFJULCYSSOP-UHFFFAOYSA-N bisoctrizole Chemical compound N1=C2C=CC=CC2=NN1C1=CC(C(C)(C)CC(C)(C)C)=CC(CC=2C(=C(C=C(C=2)C(C)(C)CC(C)(C)C)N2N=C3C=CC=CC3=N2)O)=C1O FQUNFJULCYSSOP-UHFFFAOYSA-N 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- NBBUYPNTAABDEY-UHFFFAOYSA-N cyclobutane-1,1-diol Chemical compound OC1(O)CCC1 NBBUYPNTAABDEY-UHFFFAOYSA-N 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 description 1
- TUKWPCXMNZAXLO-UHFFFAOYSA-N ethyl 2-nonylsulfanyl-4-oxo-1h-pyrimidine-6-carboxylate Chemical compound CCCCCCCCCSC1=NC(=O)C=C(C(=O)OCC)N1 TUKWPCXMNZAXLO-UHFFFAOYSA-N 0.000 description 1
- 238000004299 exfoliation Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000013467 fragmentation Methods 0.000 description 1
- 238000006062 fragmentation reaction Methods 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000001261 hydroxy acids Chemical class 0.000 description 1
- 238000009863 impact test Methods 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- CXHHBNMLPJOKQD-UHFFFAOYSA-M methyl carbonate Chemical compound COC([O-])=O CXHHBNMLPJOKQD-UHFFFAOYSA-M 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 150000007965 phenolic acids Chemical group 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920006289 polycarbonate film Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 230000004224 protection Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000009993 protective function Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 235000014214 soft drink Nutrition 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/36—Layered products comprising a layer of synthetic resin comprising polyesters
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/36—Layered products comprising a layer of synthetic resin comprising polyesters
- B32B27/365—Layered products comprising a layer of synthetic resin comprising polyesters comprising polycarbonates
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/70—Other properties
- B32B2307/71—Resistive to light or to UV
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2369/00—Polycarbonates
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/913—Material designed to be responsive to temperature, light, moisture
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31507—Of polycarbonate
Landscapes
- Laminated Bodies (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polyesters Or Polycarbonates (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/300,201 US6265072B1 (en) | 1999-04-27 | 1999-04-27 | UV-stabilized polymeric structures |
| US09/300,201 | 1999-04-27 | ||
| PCT/US2000/010361 WO2000064671A1 (en) | 1999-04-27 | 2000-04-18 | Uv-stabilized polymeric structures |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2002542087A true JP2002542087A (ja) | 2002-12-10 |
| JP2002542087A5 JP2002542087A5 (https=) | 2007-05-24 |
Family
ID=23158123
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000613645A Pending JP2002542087A (ja) | 1999-04-27 | 2000-04-18 | Ｕｖ安定化ポリマー構造物 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US6265072B1 (https=) |
| EP (1) | EP1177095B1 (https=) |
| JP (1) | JP2002542087A (https=) |
| CN (1) | CN1134341C (https=) |
| BR (1) | BR0010098A (https=) |
| DE (1) | DE60011608T2 (https=) |
| WO (1) | WO2000064671A1 (https=) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005344077A (ja) * | 2004-05-07 | 2005-12-15 | Teijin Chem Ltd | ポリカーボネート樹脂組成物およびその成形品 |
| JP2014515878A (ja) * | 2011-04-01 | 2014-07-03 | サビック・イノベーティブ・プラスチックス・アイピー・ベスローテン・フェンノートシャップ | 光電子デバイスおよびそれらのための被膜、ならびにそれらの作製および使用方法 |
| JP2015010127A (ja) * | 2013-06-27 | 2015-01-19 | 帝人株式会社 | ポリカーボネート樹脂 |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2003532752A (ja) * | 2000-04-13 | 2003-11-05 | スリーエム イノベイティブ プロパティズ カンパニー | 光安定性の製品 |
| DE10159373A1 (de) * | 2001-12-04 | 2003-06-12 | Bayer Ag | Mehrschichtiges Erzeugnis |
| US6641920B2 (en) * | 2002-02-08 | 2003-11-04 | Eastman Chemical Company | Ultraviolet protected multi-layer structures of copolyester/polycarbonate blends |
| KR20020086842A (ko) * | 2002-09-30 | 2002-11-20 | 건설화학공업(주) | 벤조옥사지논(Benzooxazinone)을 갖는 청색발광화합물 및이를 발색재료로서 채용하고 있는 유기전기 발광소자 |
| KR20020096024A (ko) * | 2002-09-30 | 2002-12-28 | 건설화학공업(주) | 벤조옥사지논(Benzooxazinone)을 갖는 바이페닐 유도체와이를 발색재료로서 채용하고 있는 유기전기 발광소자 |
| DE102005041952A1 (de) * | 2005-09-03 | 2007-03-08 | Bayer Materialscience Ag | Zusammensetzungen enthaltend Polycarbonat und neuartige UV-Absorber |
| US8418811B2 (en) * | 2006-02-21 | 2013-04-16 | Werner Co. | Fiberglass reinforced plastic products having increased weatherability, system and method |
| US9266289B2 (en) * | 2006-02-21 | 2016-02-23 | Werner Co. | Fiberglass reinforced plastic products having increased weatherability, system and method |
| ES2324586B1 (es) * | 2007-10-22 | 2010-05-31 | Novogenio S.L. | Cubierta polimerica con propiedades protectoras frente a la radiacion solar. |
| US9029461B2 (en) | 2009-02-06 | 2015-05-12 | Eastman Chemical Company | Aliphatic polyester coating compositions containing tetramethyl cyclobutanediol |
| US8324316B2 (en) * | 2009-02-06 | 2012-12-04 | Eastman Chemical Company | Unsaturated polyester resin compositions containing 2,2,2,4-tetramethyl-1,3-cyclobutanediol and articles made therefrom |
| US9029460B2 (en) | 2009-02-06 | 2015-05-12 | Stacey James Marsh | Coating compositions containing acrylic and aliphatic polyester blends |
| US8168721B2 (en) | 2009-02-06 | 2012-05-01 | Eastman Chemical Company | Coating compositions containing tetramethyl cyclobutanediol |
| US8163850B2 (en) * | 2009-02-06 | 2012-04-24 | Eastman Chemical Company | Thermosetting polyester coating compositions containing tetramethyl cyclobutanediol |
| EP2507311B1 (de) * | 2009-12-05 | 2014-08-20 | Bayer Intellectual Property GmbH | Polycarbonatzusammensetzungen mit phenolisch substituiertem triazinderivat |
| US9487619B2 (en) | 2014-10-27 | 2016-11-08 | Eastman Chemical Company | Carboxyl functional curable polyesters containing tetra-alkyl cyclobutanediol |
| US9650539B2 (en) | 2014-10-27 | 2017-05-16 | Eastman Chemical Company | Thermosetting compositions based on unsaturated polyesters and phenolic resins |
| US9598602B2 (en) | 2014-11-13 | 2017-03-21 | Eastman Chemical Company | Thermosetting compositions based on phenolic resins and curable poleyester resins made with diketene or beta-ketoacetate containing compounds |
| US20160340471A1 (en) | 2015-05-19 | 2016-11-24 | Eastman Chemical Company | Aliphatic polyester coating compositions containing tetramethyl cyclobutanediol |
| US20170088665A1 (en) | 2015-09-25 | 2017-03-30 | Eastman Chemical Company | POLYMERS CONTAINING CYCLOBUTANEDIOL AND 2,2 BIS(HYDROXYMETHYL) AlKYLCARBOXYLIC ACID |
| US9988553B2 (en) | 2016-02-22 | 2018-06-05 | Eastman Chemical Company | Thermosetting coating compositions |
| US10011737B2 (en) | 2016-03-23 | 2018-07-03 | Eastman Chemical Company | Curable polyester polyols and their use in thermosetting soft feel coating formulations |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6392644A (ja) * | 1986-10-07 | 1988-04-23 | Daicel Chem Ind Ltd | ポリカ−ボネ−ト樹脂 |
| JPH0286618A (ja) * | 1988-09-22 | 1990-03-27 | Kuraray Co Ltd | ポリカーボネート、ポリエステルカーボネートまたはポリエステルの製造方法 |
| JPH08224848A (ja) * | 1994-12-16 | 1996-09-03 | Bayer Ag | 紫外線−保護された多層ポリカーボネートシート |
| JPH08333442A (ja) * | 1995-05-31 | 1996-12-17 | Shell Internatl Res Maatschappij Bv | コポリエステル組成物 |
| WO1998019862A1 (en) * | 1996-11-04 | 1998-05-14 | Eastman Chemical Company | Uv stabilized multi-layer structures with detectable uv protective layers and a method of detection |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA807072A (en) | 1969-02-25 | A. D'onofrio Antony | Method of orienting polycarbonate resins | |
| US2465319A (en) | 1941-07-29 | 1949-03-22 | Du Pont | Polymeric linear terephthalic esters |
| US3047539A (en) | 1958-11-28 | 1962-07-31 | Goodyear Tire & Rubber | Production of polyesters |
| JPS57209979A (en) | 1981-06-19 | 1982-12-23 | Teijin Ltd | Ultraviolet light absorber and method for using same |
| US5264539A (en) | 1992-04-09 | 1993-11-23 | Hoechst Celanese Corp. | Thermally stable oligomeric ultraviolet stabilizers |
| BE1006297A3 (nl) | 1992-10-26 | 1994-07-12 | Axxis Nv | Kunststofplaat, een werkwijze voor de vervaardiging daarvan en vormdelen die de plaat bevatten. |
| US5480926A (en) | 1995-04-28 | 1996-01-02 | Eastman Chemical Company | Blends of ultraviolet absorbers and polyesters |
| EP0850914A1 (en) | 1996-12-28 | 1998-07-01 | Eastman Chemical Company | Carbonic acid 3-methoxycarbonyl-oxl-2,2,4,4-tetramethyl-cyclo-butyl ester methyl ester and method making therefor |
| US6037436A (en) * | 1996-12-28 | 2000-03-14 | Eastman Chemical Company | Process for preparing poly (2,2,4,4-tetramethyl-1,3-cyclobutylene carbonate) |
-
1999
- 1999-04-27 US US09/300,201 patent/US6265072B1/en not_active Expired - Lifetime
-
2000
- 2000-04-18 WO PCT/US2000/010361 patent/WO2000064671A1/en not_active Ceased
- 2000-04-18 DE DE2000611608 patent/DE60011608T2/de not_active Expired - Lifetime
- 2000-04-18 CN CNB008094136A patent/CN1134341C/zh not_active Expired - Fee Related
- 2000-04-18 JP JP2000613645A patent/JP2002542087A/ja active Pending
- 2000-04-18 EP EP00926074A patent/EP1177095B1/en not_active Expired - Lifetime
- 2000-04-18 BR BR0010098A patent/BR0010098A/pt not_active Application Discontinuation
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6392644A (ja) * | 1986-10-07 | 1988-04-23 | Daicel Chem Ind Ltd | ポリカ−ボネ−ト樹脂 |
| JPH0286618A (ja) * | 1988-09-22 | 1990-03-27 | Kuraray Co Ltd | ポリカーボネート、ポリエステルカーボネートまたはポリエステルの製造方法 |
| JPH08224848A (ja) * | 1994-12-16 | 1996-09-03 | Bayer Ag | 紫外線−保護された多層ポリカーボネートシート |
| JPH08333442A (ja) * | 1995-05-31 | 1996-12-17 | Shell Internatl Res Maatschappij Bv | コポリエステル組成物 |
| WO1998019862A1 (en) * | 1996-11-04 | 1998-05-14 | Eastman Chemical Company | Uv stabilized multi-layer structures with detectable uv protective layers and a method of detection |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005344077A (ja) * | 2004-05-07 | 2005-12-15 | Teijin Chem Ltd | ポリカーボネート樹脂組成物およびその成形品 |
| JP2014515878A (ja) * | 2011-04-01 | 2014-07-03 | サビック・イノベーティブ・プラスチックス・アイピー・ベスローテン・フェンノートシャップ | 光電子デバイスおよびそれらのための被膜、ならびにそれらの作製および使用方法 |
| JP2015010127A (ja) * | 2013-06-27 | 2015-01-19 | 帝人株式会社 | ポリカーボネート樹脂 |
Also Published As
| Publication number | Publication date |
|---|---|
| DE60011608D1 (de) | 2004-07-22 |
| CN1358133A (zh) | 2002-07-10 |
| US6265072B1 (en) | 2001-07-24 |
| EP1177095B1 (en) | 2004-06-16 |
| CN1134341C (zh) | 2004-01-14 |
| WO2000064671A1 (en) | 2000-11-02 |
| EP1177095A1 (en) | 2002-02-06 |
| BR0010098A (pt) | 2002-02-13 |
| DE60011608T2 (de) | 2004-10-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2002542087A (ja) | Ｕｖ安定化ポリマー構造物 | |
| CN1106935C (zh) | 具有可检测的紫外保护层的紫外稳定多层结构和检测方法 | |
| EP0595413B1 (en) | Plastic sheet, a process for the manufacture thereof and formed articles containing the sheet | |
| US6352783B1 (en) | Copolyester containing 4,4'-biphenyldicarboxylic acid, 1,4-cyclohexanedimethanol and an ultraviolet light absorbing compound and articles made therefrom | |
| EP0822962B1 (en) | Blends of ultraviolet absorbers and polyesters | |
| KR102159523B1 (ko) | 합성 수지 적층체 | |
| JPH0259341A (ja) | 改良された耐候性を有する共有押出製品 | |
| KR20020065926A (ko) | 무광택 내ｕｖ성 방염성 공압출 폴리에스테르 필름, 그용도 및 그 제조방법 | |
| CA2444474A1 (en) | Heat-absorbing layer system | |
| JP2003526711A (ja) | 結晶性熱可塑性樹脂から成る熱成型可能な耐紫外線性透明フィルム及びその使用ならびにその製造方法 | |
| JP2001270057A (ja) | ポリエステルフィルム | |
| JP2004529007A (ja) | 熱吸収性コーティング系 | |
| US6368724B1 (en) | Copolyester containing isophthalic acid, 1,4-cyclohexanedimethanol and an ultraviolet light absorbing compound and articles made therefrom | |
| JPH08225672A (ja) | ポリエチレンナフタレート成形体の蛍光防止方法 | |
| US6218450B1 (en) | Copolyester containing isophthalic acid, 1,4-cyclohexanedimethanol, 4,4′-biphenyldicarboxylic acid and an ultraviolet light absorbing compound and articles made therefrom | |
| JPWO2001038088A1 (ja) | 多層構造体 | |
| JP2003520883A (ja) | 結晶性熱可塑性樹脂から成り熱成型可能で耐紫外線性を有する白色フィルム及びその使用ならびにその製造方法 | |
| WO2009054897A1 (en) | Uv absorbing additives suitable for thermoplastic articles made from processes with extended heat histories | |
| JPH09176476A (ja) | 耐紫外線性ポリカーボネート樹脂組成物 | |
| JP4639876B2 (ja) | 耐候性に優れたポリカーボネート樹脂積層体及びその製造方法 | |
| MXPA01010804A (en) | Uv-stabilized polymeric structures | |
| JPH11179868A (ja) | ポリエチレンテレフタレート系樹脂積層体 | |
| JPH10138436A (ja) | ポリカーボネート積層シート |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20070314 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20070314 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20091228 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20100105 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20100325 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20100401 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20100928 |