GB1568531A - Reinforced polycarbonate compositions - Google Patents
Reinforced polycarbonate compositions Download PDFInfo
- Publication number
- GB1568531A GB1568531A GB12415/77A GB1241577A GB1568531A GB 1568531 A GB1568531 A GB 1568531A GB 12415/77 A GB12415/77 A GB 12415/77A GB 1241577 A GB1241577 A GB 1241577A GB 1568531 A GB1568531 A GB 1568531A
- Authority
- GB
- United Kingdom
- Prior art keywords
- bisphenol
- carbonate units
- polycarbonates
- polycarbonate
- parts
- 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
Links
- 239000004417 polycarbonate Substances 0.000 title claims description 72
- 229920000515 polycarbonate Polymers 0.000 title claims description 72
- 239000000203 mixture Substances 0.000 title claims description 61
- 239000003365 glass fiber Substances 0.000 claims description 27
- 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 claims description 19
- 229920000402 bisphenol A polycarbonate polymer Polymers 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 16
- 239000001257 hydrogen Substances 0.000 claims description 14
- 229910052739 hydrogen Inorganic materials 0.000 claims description 14
- 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 claims description 13
- 239000000460 chlorine Chemical group 0.000 claims description 11
- 229910052801 chlorine Inorganic materials 0.000 claims description 11
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 10
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 10
- 229910052794 bromium Inorganic materials 0.000 claims description 10
- 229920001577 copolymer Polymers 0.000 claims description 10
- 229920001519 homopolymer Polymers 0.000 claims description 10
- 150000002431 hydrogen Chemical group 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 8
- 239000011152 fibreglass Substances 0.000 claims description 8
- 239000001301 oxygen Substances 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 7
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical group O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 claims description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 7
- 239000000835 fiber Substances 0.000 claims description 7
- 150000002430 hydrocarbons Chemical class 0.000 claims description 7
- 230000003014 reinforcing effect Effects 0.000 claims description 7
- 238000012360 testing method Methods 0.000 claims description 6
- 229940106691 bisphenol a Drugs 0.000 claims description 5
- 239000004215 Carbon black (E152) Substances 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
- 229930195733 hydrocarbon Natural products 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 3
- 125000000732 arylene group Chemical group 0.000 claims description 3
- 125000005587 carbonate group Chemical group 0.000 claims description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims description 3
- 239000004431 polycarbonate resin Substances 0.000 claims description 3
- 229920005668 polycarbonate resin Polymers 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 125000001118 alkylidene group Chemical group 0.000 claims description 2
- 150000001412 amines Chemical class 0.000 claims description 2
- 125000002993 cycloalkylene group Chemical group 0.000 claims description 2
- 125000001033 ether group Chemical group 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 238000000465 moulding Methods 0.000 claims description 2
- 229910052698 phosphorus Inorganic materials 0.000 claims description 2
- 239000011574 phosphorus Substances 0.000 claims description 2
- 230000000704 physical effect Effects 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 19
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 9
- 239000001294 propane Substances 0.000 description 9
- -1 Parmonox Chemical class 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 5
- 239000005977 Ethylene Substances 0.000 description 5
- 239000011521 glass Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 229920001169 thermoplastic Polymers 0.000 description 4
- 239000004416 thermosoftening plastic Substances 0.000 description 4
- OWEYKIWAZBBXJK-UHFFFAOYSA-N 1,1-Dichloro-2,2-bis(4-hydroxyphenyl)ethylene Chemical group C1=CC(O)=CC=C1C(=C(Cl)Cl)C1=CC=C(O)C=C1 OWEYKIWAZBBXJK-UHFFFAOYSA-N 0.000 description 3
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000004305 biphenyl Substances 0.000 description 3
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N dimethylmethane Natural products CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000012744 reinforcing agent Substances 0.000 description 3
- 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 2
- AZZWZMUXHALBCQ-UHFFFAOYSA-N 4-[(4-hydroxy-3,5-dimethylphenyl)methyl]-2,6-dimethylphenol Chemical compound CC1=C(O)C(C)=CC(CC=2C=C(C)C(O)=C(C)C=2)=C1 AZZWZMUXHALBCQ-UHFFFAOYSA-N 0.000 description 2
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000012670 alkaline solution Substances 0.000 description 2
- 235000010290 biphenyl Nutrition 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 2
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Natural products C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000006060 molten glass Substances 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 230000002194 synthesizing effect Effects 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- FAJWQRAMGISSQY-UHFFFAOYSA-N 2,3,5,6-tetrabromo-4-[2,2-dibromo-1-(2,3,5,6-tetrabromo-4-hydroxyphenyl)ethenyl]phenol Chemical group BrC1=C(Br)C(O)=C(Br)C(Br)=C1C(=C(Br)Br)C1=C(Br)C(Br)=C(O)C(Br)=C1Br FAJWQRAMGISSQY-UHFFFAOYSA-N 0.000 description 1
- CBQXCOJLWWSCQI-UHFFFAOYSA-N 2,3,6-trichloro-4-[2,2-dichloro-1-(2,3,5-trichloro-4-hydroxyphenyl)ethenyl]phenol Chemical group ClC1=C(Cl)C(O)=C(Cl)C=C1C(=C(Cl)Cl)C1=CC(Cl)=C(O)C(Cl)=C1Cl CBQXCOJLWWSCQI-UHFFFAOYSA-N 0.000 description 1
- SJSZGSQQPBNXPY-UHFFFAOYSA-N 2,3-dibromo-4-[2-bromo-1-(2,3-dibromo-4-hydroxyphenyl)ethenyl]phenol Chemical group BrC1=C(Br)C(O)=CC=C1C(=CBr)C1=CC=C(O)C(Br)=C1Br SJSZGSQQPBNXPY-UHFFFAOYSA-N 0.000 description 1
- ZFTQHXQXEAKZRD-UHFFFAOYSA-N 2,5-dibromo-4-[2,2-dibromo-1-(2,5-dibromo-4-hydroxyphenyl)ethenyl]phenol Chemical group C1=C(Br)C(O)=CC(Br)=C1C(=C(Br)Br)C1=CC(Br)=C(O)C=C1Br ZFTQHXQXEAKZRD-UHFFFAOYSA-N 0.000 description 1
- CLYWZDGDYPXINC-UHFFFAOYSA-N 2,5-dibutyl-4-[2,2-dibromo-1-(2,5-dibutyl-4-hydroxyphenyl)ethenyl]phenol Chemical group C1=C(O)C(CCCC)=CC(C(=C(Br)Br)C=2C(=CC(O)=C(CCCC)C=2)CCCC)=C1CCCC CLYWZDGDYPXINC-UHFFFAOYSA-N 0.000 description 1
- VFVQBJRXXCJYIK-UHFFFAOYSA-N 2,6-dibromo-4-[2,2-dichloro-1-(3,5-dibromo-4-hydroxyphenyl)ethenyl]phenol Chemical group C1=C(Br)C(O)=C(Br)C=C1C(=C(Cl)Cl)C1=CC(Br)=C(O)C(Br)=C1 VFVQBJRXXCJYIK-UHFFFAOYSA-N 0.000 description 1
- JHVGTIVDWHIVQW-UHFFFAOYSA-N 2,6-dichloro-4-[2,2-dichloro-1-(3,5-dichloro-4-hydroxyphenyl)ethenyl]phenol Chemical group C1=C(Cl)C(O)=C(Cl)C=C1C(=C(Cl)Cl)C1=CC(Cl)=C(O)C(Cl)=C1 JHVGTIVDWHIVQW-UHFFFAOYSA-N 0.000 description 1
- SKJNGHJCTQYKLR-UHFFFAOYSA-N 2-bromo-4-[2,2-dibromo-1-(3-bromo-4-hydroxy-5-phenylphenyl)ethenyl]-6-phenylphenol Chemical group OC1=C(Br)C=C(C(=C(Br)Br)C=2C=C(C(O)=C(Br)C=2)C=2C=CC=CC=2)C=C1C1=CC=CC=C1 SKJNGHJCTQYKLR-UHFFFAOYSA-N 0.000 description 1
- JQNREODHWIYYHE-UHFFFAOYSA-N 2-chloro-4-[2,2-dibromo-1-(3-chloro-4-hydroxyphenyl)ethenyl]phenol Chemical group C1=C(Cl)C(O)=CC=C1C(=C(Br)Br)C1=CC=C(O)C(Cl)=C1 JQNREODHWIYYHE-UHFFFAOYSA-N 0.000 description 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical compound C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
- VWGKEVWFBOUAND-UHFFFAOYSA-N 4,4'-thiodiphenol Chemical compound C1=CC(O)=CC=C1SC1=CC=C(O)C=C1 VWGKEVWFBOUAND-UHFFFAOYSA-N 0.000 description 1
- NZGQHKSLKRFZFL-UHFFFAOYSA-N 4-(4-hydroxyphenoxy)phenol Chemical compound C1=CC(O)=CC=C1OC1=CC=C(O)C=C1 NZGQHKSLKRFZFL-UHFFFAOYSA-N 0.000 description 1
- RQCACQIALULDSK-UHFFFAOYSA-N 4-(4-hydroxyphenyl)sulfinylphenol Chemical compound C1=CC(O)=CC=C1S(=O)C1=CC=C(O)C=C1 RQCACQIALULDSK-UHFFFAOYSA-N 0.000 description 1
- MIFGCULLADMRTF-UHFFFAOYSA-N 4-[(4-hydroxy-3-methylphenyl)methyl]-2-methylphenol Chemical compound C1=C(O)C(C)=CC(CC=2C=C(C)C(O)=CC=2)=C1 MIFGCULLADMRTF-UHFFFAOYSA-N 0.000 description 1
- BATCUENAARTUKW-UHFFFAOYSA-N 4-[(4-hydroxyphenyl)-diphenylmethyl]phenol Chemical compound C1=CC(O)=CC=C1C(C=1C=CC(O)=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 BATCUENAARTUKW-UHFFFAOYSA-N 0.000 description 1
- KPASWEOQXVKOHW-UHFFFAOYSA-N 4-[2,2-dibromo-1-(2,6-diethoxy-4-hydroxyphenyl)ethenyl]-3,5-diethoxyphenol Chemical group CCOC1=CC(O)=CC(OCC)=C1C(=C(Br)Br)C1=C(OCC)C=C(O)C=C1OCC KPASWEOQXVKOHW-UHFFFAOYSA-N 0.000 description 1
- RELKRTZPXHKICN-UHFFFAOYSA-N 4-[2,2-dibromo-1-(4-hydroxyphenyl)ethenyl]phenol Chemical group C1=CC(O)=CC=C1C(=C(Br)Br)C1=CC=C(O)C=C1 RELKRTZPXHKICN-UHFFFAOYSA-N 0.000 description 1
- GYZPRLJZCUETSE-UHFFFAOYSA-N 4-[2,2-dichloro-1-(2-ethoxy-4-hydroxyphenyl)ethenyl]-3-ethoxyphenol Chemical group CCOC1=CC(O)=CC=C1C(=C(Cl)Cl)C1=CC=C(O)C=C1OCC GYZPRLJZCUETSE-UHFFFAOYSA-N 0.000 description 1
- JGVTZEQRDGLJJG-UHFFFAOYSA-N 4-[2,2-dichloro-1-(4-hydroxy-2,6-diphenylphenyl)ethenyl]-3,5-diphenylphenol Chemical group C=1C=CC=CC=1C=1C=C(O)C=C(C=2C=CC=CC=2)C=1C(=C(Cl)Cl)C=1C(C=2C=CC=CC=2)=CC(O)=CC=1C1=CC=CC=C1 JGVTZEQRDGLJJG-UHFFFAOYSA-N 0.000 description 1
- HYFYBDIXIGPGBB-UHFFFAOYSA-N 4-[2,2-dichloro-1-(4-hydroxy-3-methylphenyl)ethenyl]-2-methylphenol Chemical group C1=C(O)C(C)=CC(C(=C(Cl)Cl)C=2C=C(C)C(O)=CC=2)=C1 HYFYBDIXIGPGBB-UHFFFAOYSA-N 0.000 description 1
- RGFOLKNZEXLIEN-UHFFFAOYSA-N 4-[2-bromo-1-(4-hydroxy-3,5-dimethoxyphenyl)ethenyl]-2,6-dimethoxyphenol Chemical group COC1=C(O)C(OC)=CC(C(=CBr)C=2C=C(OC)C(O)=C(OC)C=2)=C1 RGFOLKNZEXLIEN-UHFFFAOYSA-N 0.000 description 1
- WKBIXHAFOKAQAX-UHFFFAOYSA-N 4-[2-bromo-1-(4-hydroxy-3,5-diphenylphenyl)ethenyl]-2,6-diphenylphenol Chemical group OC1=C(C=2C=CC=CC=2)C=C(C(=CBr)C=2C=C(C(O)=C(C=2)C=2C=CC=CC=2)C=2C=CC=CC=2)C=C1C1=CC=CC=C1 WKBIXHAFOKAQAX-UHFFFAOYSA-N 0.000 description 1
- ZBANSWARHYAFCF-UHFFFAOYSA-N 4-[2-chloro-1-(4-hydroxy-3-methoxyphenyl)ethenyl]-2-methoxyphenol Chemical group C1=C(O)C(OC)=CC(C(=CCl)C=2C=C(OC)C(O)=CC=2)=C1 ZBANSWARHYAFCF-UHFFFAOYSA-N 0.000 description 1
- LDHBQMQZCBBPCC-UHFFFAOYSA-N 4-[2-chloro-1-[4-hydroxy-3,5-di(propan-2-yl)phenyl]ethenyl]-2,6-di(propan-2-yl)phenol Chemical group CC(C)C1=C(O)C(C(C)C)=CC(C(=CCl)C=2C=C(C(O)=C(C(C)C)C=2)C(C)C)=C1 LDHBQMQZCBBPCC-UHFFFAOYSA-N 0.000 description 1
- OXAYRNCOAPIHLJ-UHFFFAOYSA-N 4-[3,3-bis(5-tert-butyl-4-hydroxy-2-methylphenyl)butan-2-yl]-2-tert-butyl-5-methylphenol Chemical compound C=1C(C(C)(C)C)=C(O)C=C(C)C=1C(C)(C=1C(=CC(O)=C(C=1)C(C)(C)C)C)C(C)C1=CC(C(C)(C)C)=C(O)C=C1C OXAYRNCOAPIHLJ-UHFFFAOYSA-N 0.000 description 1
- BLPODHBKBPRTPG-UHFFFAOYSA-N 4-[[3,5-bis[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]phenyl]methyl]-2,6-ditert-butylphenol Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CC=2C=C(CC=3C=C(C(O)=C(C=3)C(C)(C)C)C(C)(C)C)C=C(CC=3C=C(C(O)=C(C=3)C(C)(C)C)C(C)(C)C)C=2)=C1 BLPODHBKBPRTPG-UHFFFAOYSA-N 0.000 description 1
- HJXUQPWAJAIRJK-UHFFFAOYSA-N 5-chloro-4-[2,2-dichloro-1-(2-chloro-5-ethyl-4-hydroxyphenyl)ethenyl]-2-ethylphenol Chemical group C1=C(O)C(CC)=CC(C(=C(Cl)Cl)C=2C(=CC(O)=C(CC)C=2)Cl)=C1Cl HJXUQPWAJAIRJK-UHFFFAOYSA-N 0.000 description 1
- UMHJEEQLYBKSAN-UHFFFAOYSA-N Adipaldehyde Chemical compound O=CCCCCC=O UMHJEEQLYBKSAN-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
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical group Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- VCCBEIPGXKNHFW-UHFFFAOYSA-N biphenyl-4,4'-diol Chemical group C1=CC(O)=CC=C1C1=CC=C(O)C=C1 VCCBEIPGXKNHFW-UHFFFAOYSA-N 0.000 description 1
- 239000005388 borosilicate glass Substances 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- ZNWNWEHQFXOPGK-UHFFFAOYSA-N decanedial Chemical compound O=CCCCCCCCCC=O ZNWNWEHQFXOPGK-UHFFFAOYSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000001282 iso-butane Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- MNZMMCVIXORAQL-UHFFFAOYSA-N naphthalene-2,6-diol Chemical compound C1=C(O)C=CC2=CC(O)=CC=C21 MNZMMCVIXORAQL-UHFFFAOYSA-N 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- QIIPQYDSKRYMFG-UHFFFAOYSA-N phenyl hydrogen carbonate Chemical group OC(=O)OC1=CC=CC=C1 QIIPQYDSKRYMFG-UHFFFAOYSA-N 0.000 description 1
- DOIRQSBPFJWKBE-UHFFFAOYSA-N phthalic acid di-n-butyl ester Natural products CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 239000003340 retarding agent Substances 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000012815 thermoplastic material Substances 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
- C08K7/00—Use of ingredients characterised by shape
- C08K7/02—Fibres or whiskers
- C08K7/04—Fibres or whiskers inorganic
- C08K7/14—Glass
Landscapes
- 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)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19681766792D DE1766792B1 (de) | 1968-07-12 | 1968-07-19 | Chirurgisches Geraet zum Vernaehen von Hohlorganen Kleinen Durchmessers |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US67241576A | 1976-03-31 | 1976-03-31 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1568531A true GB1568531A (en) | 1980-05-29 |
Family
ID=24698453
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB12415/77A Expired GB1568531A (en) | 1968-07-12 | 1977-03-24 | Reinforced polycarbonate compositions |
Country Status (12)
| Country | Link |
|---|---|
| JP (1) | JPS52128945A (enExample) |
| AU (1) | AU512822B2 (enExample) |
| BE (1) | BE852979A (enExample) |
| BR (1) | BR7701902A (enExample) |
| DD (1) | DD130044A5 (enExample) |
| DE (1) | DE2709389A1 (enExample) |
| FR (1) | FR2346405A1 (enExample) |
| GB (1) | GB1568531A (enExample) |
| IN (1) | IN146075B (enExample) |
| MX (1) | MX145405A (enExample) |
| NL (1) | NL7703417A (enExample) |
| PL (1) | PL102952B1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4980426A (en) * | 1988-10-15 | 1990-12-25 | Bayer Aktiengesellschaft | Moulding compounds of polycarbonate mixtures having a high disperse solubility |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1386583A (fr) * | 1964-01-10 | 1965-01-22 | Bayer Ag | Procédé de préparation de matières artificielles thermoplastiques renforcées par des fibres de verre |
| DE1201991C2 (de) * | 1964-03-12 | 1979-03-01 | Bayer Ag, 5090 Leverkusen | Herstellen von glasfaserhaltigem granulat aus hochmolekularen, thermoplastisschen polycarbonaten |
-
1977
- 1977-02-25 AU AU22708/77A patent/AU512822B2/en not_active Expired
- 1977-02-28 IN IN287/CAL/77A patent/IN146075B/en unknown
- 1977-03-04 DE DE19772709389 patent/DE2709389A1/de not_active Withdrawn
- 1977-03-24 GB GB12415/77A patent/GB1568531A/en not_active Expired
- 1977-03-25 BR BR7701902A patent/BR7701902A/pt unknown
- 1977-03-28 FR FR7709164A patent/FR2346405A1/fr not_active Withdrawn
- 1977-03-29 NL NL7703417A patent/NL7703417A/xx not_active Application Discontinuation
- 1977-03-29 BE BE176197A patent/BE852979A/xx unknown
- 1977-03-29 PL PL1977196999A patent/PL102952B1/pl unknown
- 1977-03-29 DD DD7700198127A patent/DD130044A5/xx unknown
- 1977-03-31 JP JP3552177A patent/JPS52128945A/ja active Pending
- 1977-03-31 MX MX168599A patent/MX145405A/es unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4980426A (en) * | 1988-10-15 | 1990-12-25 | Bayer Aktiengesellschaft | Moulding compounds of polycarbonate mixtures having a high disperse solubility |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2270877A (en) | 1978-08-31 |
| IN146075B (enExample) | 1979-02-17 |
| PL102952B1 (pl) | 1979-05-31 |
| AU512822B2 (en) | 1980-10-30 |
| BR7701902A (pt) | 1977-11-08 |
| NL7703417A (nl) | 1977-10-04 |
| MX145405A (es) | 1982-02-04 |
| DE2709389A1 (de) | 1977-10-13 |
| JPS52128945A (en) | 1977-10-28 |
| FR2346405A1 (fr) | 1977-10-28 |
| BE852979A (fr) | 1977-07-18 |
| DD130044A5 (de) | 1978-03-01 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |