DE60223842T2 - Lichtdurchlässige flammhemmende polycarbonat-harzzusammensetzungen - Google Patents
Lichtdurchlässige flammhemmende polycarbonat-harzzusammensetzungen Download PDFInfo
- Publication number
- DE60223842T2 DE60223842T2 DE60223842T DE60223842T DE60223842T2 DE 60223842 T2 DE60223842 T2 DE 60223842T2 DE 60223842 T DE60223842 T DE 60223842T DE 60223842 T DE60223842 T DE 60223842T DE 60223842 T2 DE60223842 T2 DE 60223842T2
- Authority
- DE
- Germany
- Prior art keywords
- polycarbonate
- equal
- composition
- sulfonic acid
- less
- 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.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title claims description 46
- 229920005668 polycarbonate resin Polymers 0.000 title claims description 17
- 239000004431 polycarbonate resin Substances 0.000 title claims description 17
- 239000004417 polycarbonate Substances 0.000 claims description 50
- 229920000515 polycarbonate Polymers 0.000 claims description 45
- -1 Polytetrafluoroethylene Polymers 0.000 claims description 44
- 239000003063 flame retardant Substances 0.000 claims description 20
- 229920005989 resin Polymers 0.000 claims description 17
- 239000011347 resin Substances 0.000 claims description 17
- 239000004810 polytetrafluoroethylene Substances 0.000 claims description 15
- 229920001343 polytetrafluoroethylene Polymers 0.000 claims description 15
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims description 11
- 125000003118 aryl group Chemical group 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 5
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 4
- 229910052794 bromium Inorganic materials 0.000 claims description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
- 125000001931 aliphatic group Chemical group 0.000 claims description 3
- 239000003513 alkali Substances 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims description 3
- 230000005540 biological transmission Effects 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 239000000460 chlorine Substances 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims 10
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical class CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims 1
- 150000008430 aromatic amides Chemical class 0.000 claims 1
- 150000008365 aromatic ketones Chemical class 0.000 claims 1
- 150000008378 aryl ethers Chemical class 0.000 claims 1
- RMGVZKRVHHSUIM-UHFFFAOYSA-N dithionic acid Chemical compound OS(=O)(=O)S(O)(=O)=O RMGVZKRVHHSUIM-UHFFFAOYSA-N 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical class C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 10
- 125000004432 carbon atom Chemical group C* 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 238000001746 injection moulding Methods 0.000 description 5
- 230000035699 permeability Effects 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- 239000006085 branching agent Substances 0.000 description 4
- 125000001183 hydrocarbyl group Chemical group 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 150000003254 radicals Chemical class 0.000 description 4
- 150000003460 sulfonic acids Chemical class 0.000 description 4
- VSIKJPJINIDELZ-UHFFFAOYSA-N 2,2,4,4,6,6,8,8-octakis-phenyl-1,3,5,7,2,4,6,8-tetraoxatetrasilocane Chemical compound O1[Si](C=2C=CC=CC=2)(C=2C=CC=CC=2)O[Si](C=2C=CC=CC=2)(C=2C=CC=CC=2)O[Si](C=2C=CC=CC=2)(C=2C=CC=CC=2)O[Si]1(C=1C=CC=CC=1)C1=CC=CC=C1 VSIKJPJINIDELZ-UHFFFAOYSA-N 0.000 description 3
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229950003332 perflubutane Drugs 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- LVTHXRLARFLXNR-UHFFFAOYSA-M potassium;1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate Chemical compound [K+].[O-]S(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F LVTHXRLARFLXNR-UHFFFAOYSA-M 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- PXKLMJQFEQBVLD-UHFFFAOYSA-N Bisphenol F Natural products C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 229920000402 bisphenol A polycarbonate polymer Polymers 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 125000005027 hydroxyaryl group Chemical group 0.000 description 2
- KAVGMUDTWQVPDF-UHFFFAOYSA-N perflubutane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)F KAVGMUDTWQVPDF-UHFFFAOYSA-N 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 2
- HCNHNBLSNVSJTJ-UHFFFAOYSA-N 1,1-Bis(4-hydroxyphenyl)ethane Chemical compound C=1C=C(O)C=CC=1C(C)C1=CC=C(O)C=C1 HCNHNBLSNVSJTJ-UHFFFAOYSA-N 0.000 description 1
- YKPAABNCNAGAAJ-UHFFFAOYSA-N 1,1-Bis(4-hydroxyphenyl)propane Chemical compound C=1C=C(O)C=CC=1C(CC)C1=CC=C(O)C=C1 YKPAABNCNAGAAJ-UHFFFAOYSA-N 0.000 description 1
- MAQOZOILPAMFSW-UHFFFAOYSA-N 2,6-bis[(2-hydroxy-5-methylphenyl)methyl]-4-methylphenol Chemical compound CC1=CC=C(O)C(CC=2C(=C(CC=3C(=CC=C(C)C=3)O)C=C(C)C=2)O)=C1 MAQOZOILPAMFSW-UHFFFAOYSA-N 0.000 description 1
- YNNMNWHCQGBNFH-UHFFFAOYSA-N 3-tert-butyl-4-[1-(2-tert-butyl-4-hydroxyphenyl)propyl]phenol Chemical compound C=1C=C(O)C=C(C(C)(C)C)C=1C(CC)C1=CC=C(O)C=C1C(C)(C)C YNNMNWHCQGBNFH-UHFFFAOYSA-N 0.000 description 1
- GXDIDDARPBFKNG-UHFFFAOYSA-N 4,4'-(Butane-1,1-diyl)diphenol Chemical compound C=1C=C(O)C=CC=1C(CCC)C1=CC=C(O)C=C1 GXDIDDARPBFKNG-UHFFFAOYSA-N 0.000 description 1
- RSSGMIIGVQRGDS-UHFFFAOYSA-N 4-[(4-hydroxyphenyl)-phenylmethyl]phenol Chemical compound C1=CC(O)=CC=C1C(C=1C=CC(O)=CC=1)C1=CC=CC=C1 RSSGMIIGVQRGDS-UHFFFAOYSA-N 0.000 description 1
- OVVCSFQRAXVPGT-UHFFFAOYSA-N 4-[1-(4-hydroxyphenyl)cyclopentyl]phenol Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)CCCC1 OVVCSFQRAXVPGT-UHFFFAOYSA-N 0.000 description 1
- YTRKBSVUOQIJOR-UHFFFAOYSA-N 4-[2-(4-hydroxy-1-methylcyclohexa-2,4-dien-1-yl)propan-2-yl]-4-methylcyclohexa-1,5-dien-1-ol Chemical compound C1C=C(O)C=CC1(C)C(C)(C)C1(C)CC=C(O)C=C1 YTRKBSVUOQIJOR-UHFFFAOYSA-N 0.000 description 1
- QHJPJZROUNGTRJ-UHFFFAOYSA-N 4-[2-(4-hydroxyphenyl)octan-2-yl]phenol Chemical compound C=1C=C(O)C=CC=1C(C)(CCCCCC)C1=CC=C(O)C=C1 QHJPJZROUNGTRJ-UHFFFAOYSA-N 0.000 description 1
- PREWTCFQARLUPB-UHFFFAOYSA-N 4-[2-[3,5-bis[2-(4-hydroxyphenyl)propan-2-yl]phenyl]propan-2-yl]phenol Chemical compound C=1C(C(C)(C)C=2C=CC(O)=CC=2)=CC(C(C)(C)C=2C=CC(O)=CC=2)=CC=1C(C)(C)C1=CC=C(O)C=C1 PREWTCFQARLUPB-UHFFFAOYSA-N 0.000 description 1
- HTVITOHKHWFJKO-UHFFFAOYSA-N Bisphenol B Chemical compound C=1C=C(O)C=CC=1C(C)(CC)C1=CC=C(O)C=C1 HTVITOHKHWFJKO-UHFFFAOYSA-N 0.000 description 1
- SDDLEVPIDBLVHC-UHFFFAOYSA-N Bisphenol Z Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)CCCCC1 SDDLEVPIDBLVHC-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- COVZYZSDYWQREU-UHFFFAOYSA-N Busulfan Chemical class CS(=O)(=O)OCCCCOS(C)(=O)=O COVZYZSDYWQREU-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- XQDFANVFBMSJGF-UHFFFAOYSA-N FC1=C(C=C(C(=C1)F)F)S(=O)(=O)OC1=C(C(=CC=C1)F)F.[K] Chemical compound FC1=C(C=C(C(=C1)F)F)S(=O)(=O)OC1=C(C(=CC=C1)F)F.[K] XQDFANVFBMSJGF-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- OCKWAZCWKSMKNC-UHFFFAOYSA-N [3-octadecanoyloxy-2,2-bis(octadecanoyloxymethyl)propyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCCCCCC)(COC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC OCKWAZCWKSMKNC-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- DCBMHXCACVDWJZ-UHFFFAOYSA-N adamantylidene Chemical group C1C(C2)CC3[C]C1CC2C3 DCBMHXCACVDWJZ-UHFFFAOYSA-N 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000002102 aryl alkyloxo group Chemical group 0.000 description 1
- 150000005840 aryl radicals Chemical class 0.000 description 1
- 125000004104 aryloxy group Chemical group 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-M benzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-M 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 1
- 150000001924 cycloalkanes Chemical class 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- JPWJQIKXWASNOD-UHFFFAOYSA-N cycloheptylidenecycloheptane Chemical group C1CCCCCC1=C1CCCCCC1 JPWJQIKXWASNOD-UHFFFAOYSA-N 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000012217 deletion Methods 0.000 description 1
- 230000037430 deletion Effects 0.000 description 1
- FPFJTBQQZWBMAZ-UHFFFAOYSA-L disodium;2,2,3,3,4,4-hexafluoropentanedioate Chemical compound [Na+].[Na+].[O-]C(=O)C(F)(F)C(F)(F)C(F)(F)C([O-])=O FPFJTBQQZWBMAZ-UHFFFAOYSA-L 0.000 description 1
- WZZLWPIYWZEJOX-UHFFFAOYSA-L disodium;naphthalene-2,6-disulfonate Chemical compound [Na+].[Na+].C1=C(S([O-])(=O)=O)C=CC2=CC(S(=O)(=O)[O-])=CC=C21 WZZLWPIYWZEJOX-UHFFFAOYSA-L 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000007323 disproportionation reaction Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- 125000005067 haloformyl group Chemical group 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000010406 interfacial reaction Methods 0.000 description 1
- 238000006317 isomerization reaction Methods 0.000 description 1
- 125000000654 isopropylidene group Chemical group C(C)(C)=* 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- SJDACOMXKWHBOW-UHFFFAOYSA-N oxyphenisatine Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2NC1=O SJDACOMXKWHBOW-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920001230 polyarylate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- GLGXXYFYZWQGEL-UHFFFAOYSA-M potassium;trifluoromethanesulfonate Chemical compound [K+].[O-]S(=O)(=O)C(F)(F)F GLGXXYFYZWQGEL-UHFFFAOYSA-M 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 229930195734 saturated hydrocarbon Chemical group 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- QBJDFZSOZNDVDE-UHFFFAOYSA-M sodium;1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate Chemical group [Na+].[O-]S(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F QBJDFZSOZNDVDE-UHFFFAOYSA-M 0.000 description 1
- GNMQSINWSMAMIQ-UHFFFAOYSA-N sodium;2,4,6-trifluoro-3,5-bis(methoxycarbonyl)benzenesulfonic acid Chemical compound [Na].COC(=O)C1=C(F)C(C(=O)OC)=C(F)C(S(O)(=O)=O)=C1F GNMQSINWSMAMIQ-UHFFFAOYSA-N 0.000 description 1
- YVJJXAJZVSZHTN-UHFFFAOYSA-M sodium;2,5-difluorothiophene-3-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)C=1C=C(F)SC=1F YVJJXAJZVSZHTN-UHFFFAOYSA-M 0.000 description 1
- VJZDBZOTAGNXCT-UHFFFAOYSA-M sodium;2-fluoro-5-(4-fluorophenyl)benzenesulfonate Chemical compound [Na+].C1=C(F)C(S(=O)(=O)[O-])=CC(C=2C=CC(F)=CC=2)=C1 VJZDBZOTAGNXCT-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229920000638 styrene acrylonitrile Polymers 0.000 description 1
- 239000011145 styrene acrylonitrile resin Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 description 1
- NJMOHBDCGXJLNJ-UHFFFAOYSA-N trimellitic anhydride chloride Chemical compound ClC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 NJMOHBDCGXJLNJ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/54—Silicon-containing compounds
- C08K5/541—Silicon-containing compounds containing oxygen
- C08K5/5415—Silicon-containing compounds containing oxygen containing at least one Si—O bond
- C08K5/5419—Silicon-containing compounds containing oxygen containing at least one Si—O bond containing at least one Si—C bond
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/02—Halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/15—Heterocyclic compounds having oxygen in the ring
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/41—Compounds containing sulfur bound to oxygen
- C08K5/42—Sulfonic acids; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/12—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US683288 | 2001-12-10 | ||
| US09/683,288 US6462111B1 (en) | 2001-12-10 | 2001-12-10 | Translucent flame retardant polycarbonate compositions |
| PCT/US2002/035521 WO2003050176A1 (en) | 2001-12-10 | 2002-11-04 | Translucent flame retardant polycarbonate compositions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE60223842D1 DE60223842D1 (de) | 2008-01-10 |
| DE60223842T2 true DE60223842T2 (de) | 2008-10-09 |
Family
ID=24743369
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE60223842T Expired - Lifetime DE60223842T2 (de) | 2001-12-10 | 2002-11-04 | Lichtdurchlässige flammhemmende polycarbonat-harzzusammensetzungen |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US6462111B1 (https=) |
| EP (1) | EP1458799B1 (https=) |
| JP (2) | JP2005511843A (https=) |
| KR (1) | KR100899506B1 (https=) |
| CN (1) | CN100366668C (https=) |
| AU (1) | AU2002350134A1 (https=) |
| DE (1) | DE60223842T2 (https=) |
| TW (1) | TWI287558B (https=) |
| WO (1) | WO2003050176A1 (https=) |
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|---|---|---|---|---|
| EP4092075A1 (de) * | 2021-05-17 | 2022-11-23 | Covestro Deutschland AG | Flammwidrige zusammensetzung umfassend 0,040 bis 0,095 gew.-% eines flammschutzmittels |
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| US20050009968A1 (en) * | 2003-06-28 | 2005-01-13 | General Electric Company | Transparent Flame Retardant Polycarbonate Compositions |
| EP1670349B9 (en) | 2003-10-03 | 2014-01-15 | Applied Medical Resources Corporation | Bladeless optical obturator |
| EP3431026B1 (en) | 2004-06-29 | 2020-09-23 | Applied Medical Resources Corporation | Insufflating optical surgical instrument |
| US7794644B2 (en) * | 2005-10-05 | 2010-09-14 | Applied Medical Resources Corporation | Thin-walled optical obturator |
| US20080015292A1 (en) * | 2006-07-12 | 2008-01-17 | General Electric Company | Flame retardant and scratch resistant thermoplastic polycarbonate compositions |
| WO2008043100A2 (en) | 2006-10-06 | 2008-04-10 | Applied Medical Resources Corporation | Visual insufflation port |
| JP5612242B2 (ja) * | 2007-05-31 | 2014-10-22 | 帝人株式会社 | 難燃性ポリカーボネート樹脂組成物 |
| JP5583883B2 (ja) * | 2007-05-31 | 2014-09-03 | 帝人株式会社 | 難燃性ポリカーボネート樹脂組成物 |
| US20090062438A1 (en) * | 2007-08-30 | 2009-03-05 | Van De Grampel Robert Dirk | Copolyestercarbonate compositions |
| US20090062439A1 (en) * | 2007-08-30 | 2009-03-05 | Van De Grampel Robert Dirk | Polyestercarbonate compositions |
| EP2837345B1 (en) | 2008-01-25 | 2016-10-05 | Applied Medical Resources Corporation | Insufflating access system |
| US9570211B2 (en) * | 2008-08-27 | 2017-02-14 | Covestro Llc | Transparent thermoplastic composition with improved electrical conductivity in the melt |
| EP2328487B1 (en) | 2008-09-29 | 2018-04-18 | Applied Medical Resources Corporation | First-entry trocar system |
| CN102666703B (zh) * | 2009-11-05 | 2014-12-24 | 拜尔材料科学股份公司 | 具有改进的阻燃性的聚碳酸酯板 |
| CN101704994B (zh) * | 2009-12-15 | 2012-01-18 | 重庆启蓝塑料有限公司 | 一种透明阻燃聚碳酸酯(pc)材料及其制备方法 |
| CN101851407B (zh) * | 2010-03-09 | 2013-08-07 | 上海锦湖日丽塑料有限公司 | 高表面光泽玻璃纤维增强阻燃聚碳酸脂组合物及制备方法 |
| EP2640782B1 (en) * | 2010-11-15 | 2021-04-07 | SHPP Global Technologies B.V. | Compositions and articles of manufacture containing siloxane |
| JP5267582B2 (ja) * | 2011-01-21 | 2013-08-21 | 三菱エンジニアリングプラスチックス株式会社 | 難燃性ポリカーボネート樹脂組成物及びこれを用いた成形体 |
| US9234096B2 (en) * | 2011-02-03 | 2016-01-12 | Sabic Global Technologies B.V. | Color and heat stable polycarbonate compositions and methods of making |
| US9453128B2 (en) | 2011-03-31 | 2016-09-27 | Sabic Global Technologies B.V. | Rail component comprising flame retardant compositions, and methods of manufacture |
| US9006324B2 (en) | 2011-03-31 | 2015-04-14 | Sabic Global Technologies B.V. | Flame retardant polycarbonate compositions, methods of manufacture, and articles formed therefrom |
| US8981015B2 (en) | 2011-03-31 | 2015-03-17 | Sabic Global Technologies B.V. | Flame retardant poly(siloxane) copolymer compositions, methods of manufacture, and articles formed therefrom |
| US8703855B2 (en) | 2011-03-31 | 2014-04-22 | Sabic Innovative Plastics Ip B.V. | Electrical tracking resistance compositions, methods and articles of manufacture |
| US8703856B2 (en) | 2011-03-31 | 2014-04-22 | Sabic Innovative Plastics Ip B.V. | Electrical tracking resistance compositions, methods and articles of manufacture |
| US9254148B2 (en) | 2011-05-02 | 2016-02-09 | Applied Medical Resources Corporation | Low-profile surgical universal access port |
| US8937127B2 (en) | 2011-09-30 | 2015-01-20 | Sabic Global Technologies B.V. | Flame retardant poly(siloxane-etherimide) copolymer compositions, methods of manufacture, and articles formed therefrom |
| US9127155B2 (en) | 2012-04-11 | 2015-09-08 | Sabic Global Technologies B.V. | Phosphorus free flame retardant composition |
| US8691915B2 (en) | 2012-04-23 | 2014-04-08 | Sabic Innovative Plastics Ip B.V. | Copolymers and polymer blends having improved refractive indices |
| US8877876B2 (en) * | 2012-06-29 | 2014-11-04 | Sabic Global Technologies B.V. | High-temperature plastic article |
| KR101402579B1 (ko) * | 2013-10-25 | 2014-05-30 | 주식회사 엘지화학 | 투명성과 난연성이 우수한 폴리카보네이트 수지 조성물 |
| WO2015140671A1 (en) * | 2014-03-20 | 2015-09-24 | Sabic Global Technologies B.V. | Polycarbonate compositions, methods of their manufacture, and articles thereof |
| US10005903B2 (en) | 2015-03-09 | 2018-06-26 | Sabic Global Technologies B.V. | Compositions and articles of manufacture containing branched polycarbonate |
| EP3320018B1 (en) * | 2015-07-09 | 2022-08-10 | SHPP Global Technologies B.V. | Polycarbonate compositions with improved flame retardance |
| KR20180071325A (ko) * | 2015-11-04 | 2018-06-27 | 사빅 글로벌 테크놀러지스 비.브이. | 광학 부품의 난연 특성, 발광 효율 및 빔 각도가 향상된 확산성 폴리카보네이트 복합체 |
| KR102007100B1 (ko) * | 2017-12-29 | 2019-08-02 | 롯데첨단소재(주) | 열가소성 수지 조성물 및 이로부터 형성된 성형품 |
| JP7252727B2 (ja) * | 2018-09-14 | 2023-04-05 | 出光興産株式会社 | ポリカーボネート系樹脂組成物 |
| CN112063148A (zh) * | 2020-09-16 | 2020-12-11 | 横店集团得邦工程塑料有限公司 | 一种具有高阻燃性能的耐水解pc复合材料及其制备方法 |
| EP4092070A1 (de) | 2021-05-17 | 2022-11-23 | Covestro Deutschland AG | Reduzierung des gehalts spezieller salze von sulfonsäure-, sulfonamiden- oder sulfonimidderivaten im abwasser |
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-
2001
- 2001-12-10 US US09/683,288 patent/US6462111B1/en not_active Expired - Lifetime
-
2002
- 2002-11-04 WO PCT/US2002/035521 patent/WO2003050176A1/en not_active Ceased
- 2002-11-04 KR KR1020047008940A patent/KR100899506B1/ko not_active Expired - Fee Related
- 2002-11-04 EP EP02786662A patent/EP1458799B1/en not_active Expired - Lifetime
- 2002-11-04 DE DE60223842T patent/DE60223842T2/de not_active Expired - Lifetime
- 2002-11-04 AU AU2002350134A patent/AU2002350134A1/en not_active Abandoned
- 2002-11-04 CN CNB028277805A patent/CN100366668C/zh not_active Expired - Fee Related
- 2002-11-04 JP JP2003551198A patent/JP2005511843A/ja active Pending
- 2002-11-27 TW TW091134519A patent/TWI287558B/zh active
-
2010
- 2010-07-02 JP JP2010152059A patent/JP5480041B2/ja not_active Expired - Fee Related
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP4092075A1 (de) * | 2021-05-17 | 2022-11-23 | Covestro Deutschland AG | Flammwidrige zusammensetzung umfassend 0,040 bis 0,095 gew.-% eines flammschutzmittels |
| WO2022243223A1 (de) | 2021-05-17 | 2022-11-24 | Covestro Deutschland Ag | Flammwidrige zusammensetzung umfassend 0,040 bis 0,095 gew.-% eines flammschutzmittels |
| WO2022243222A1 (de) | 2021-05-17 | 2022-11-24 | Covestro Deutschland Ag | Flammwidrige zusammensetzung umfassend 0,040 bis 0,095 gew.-% eines flammschutzmittels |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1458799A1 (en) | 2004-09-22 |
| JP5480041B2 (ja) | 2014-04-23 |
| KR20040071714A (ko) | 2004-08-12 |
| JP2005511843A (ja) | 2005-04-28 |
| JP2010248527A (ja) | 2010-11-04 |
| CN100366668C (zh) | 2008-02-06 |
| US6462111B1 (en) | 2002-10-08 |
| EP1458799B1 (en) | 2007-11-28 |
| AU2002350134A1 (en) | 2003-06-23 |
| KR100899506B1 (ko) | 2009-05-26 |
| TW200300782A (en) | 2003-06-16 |
| WO2003050176A1 (en) | 2003-06-19 |
| DE60223842D1 (de) | 2008-01-10 |
| CN1617905A (zh) | 2005-05-18 |
| TWI287558B (en) | 2007-10-01 |
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