MXPA05005974A - Masas del moldeo de policarbonato. - Google Patents
Masas del moldeo de policarbonato.Info
- Publication number
- MXPA05005974A MXPA05005974A MXPA05005974A MXPA05005974A MXPA05005974A MX PA05005974 A MXPA05005974 A MX PA05005974A MX PA05005974 A MXPA05005974 A MX PA05005974A MX PA05005974 A MXPA05005974 A MX PA05005974A MX PA05005974 A MXPA05005974 A MX PA05005974A
- Authority
- MX
- Mexico
- Prior art keywords
- compositions according
- carbon atoms
- weight
- compositions
- contain
- Prior art date
Links
- 239000004417 polycarbonate Substances 0.000 title claims abstract description 45
- 229920000515 polycarbonate Polymers 0.000 title claims abstract description 40
- 150000001875 compounds Chemical class 0.000 title claims description 13
- 238000000465 moulding Methods 0.000 title description 10
- 239000000203 mixture Substances 0.000 claims abstract description 83
- 229920000578 graft copolymer Polymers 0.000 claims abstract description 30
- 125000003118 aryl group Chemical group 0.000 claims abstract description 23
- 229920000642 polymer Polymers 0.000 claims abstract description 21
- 229920000728 polyester Polymers 0.000 claims abstract description 14
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims abstract description 12
- 239000000178 monomer Substances 0.000 claims abstract description 9
- 229920002857 polybutadiene Polymers 0.000 claims abstract description 8
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims abstract description 7
- 125000000524 functional group Chemical group 0.000 claims abstract description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 39
- 229920001971 elastomer Polymers 0.000 claims description 28
- 239000005060 rubber Substances 0.000 claims description 27
- 125000000217 alkyl group Chemical group 0.000 claims description 20
- -1 aromatic poly (ester Chemical class 0.000 claims description 19
- 229920000098 polyolefin Polymers 0.000 claims description 16
- 239000006085 branching agent Substances 0.000 claims description 13
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 10
- 239000000654 additive Substances 0.000 claims description 10
- 239000002245 particle Substances 0.000 claims description 10
- 150000002148 esters Chemical class 0.000 claims description 9
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- 239000002904 solvent Substances 0.000 claims description 8
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims description 7
- 229920001296 polysiloxane Polymers 0.000 claims description 7
- ZEKCYPANSOJWDH-UHFFFAOYSA-N 3,3-bis(4-hydroxy-3-methylphenyl)-1H-indol-2-one Chemical compound C1=C(O)C(C)=CC(C2(C3=CC=CC=C3NC2=O)C=2C=C(C)C(O)=CC=2)=C1 ZEKCYPANSOJWDH-UHFFFAOYSA-N 0.000 claims description 6
- 239000003381 stabilizer Substances 0.000 claims description 6
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims description 5
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 5
- 229920001577 copolymer Polymers 0.000 claims description 5
- 238000007720 emulsion polymerization reaction Methods 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- 150000002367 halogens Chemical class 0.000 claims description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 4
- 239000000835 fiber Substances 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 229910052698 phosphorus Inorganic materials 0.000 claims description 4
- 239000011574 phosphorus Substances 0.000 claims description 4
- XKZQKPRCPNGNFR-UHFFFAOYSA-N 2-(3-hydroxyphenyl)phenol Chemical compound OC1=CC=CC(C=2C(=CC=CC=2)O)=C1 XKZQKPRCPNGNFR-UHFFFAOYSA-N 0.000 claims description 3
- 150000008360 acrylonitriles Chemical class 0.000 claims description 3
- 150000001412 amines Chemical group 0.000 claims description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 3
- 150000003008 phosphonic acid esters Chemical class 0.000 claims description 3
- 229920002943 EPDM rubber Polymers 0.000 claims description 2
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000006096 absorbing agent Substances 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 239000003963 antioxidant agent Substances 0.000 claims description 2
- 239000004760 aramid Substances 0.000 claims description 2
- 229920006231 aramid fiber Polymers 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 239000000975 dye Substances 0.000 claims description 2
- 239000003822 epoxy resin Substances 0.000 claims description 2
- 239000000945 filler Substances 0.000 claims description 2
- 239000012757 flame retardant agent Substances 0.000 claims description 2
- 239000004088 foaming agent Substances 0.000 claims description 2
- 239000012760 heat stabilizer Substances 0.000 claims description 2
- 230000007062 hydrolysis Effects 0.000 claims description 2
- 238000006460 hydrolysis reaction Methods 0.000 claims description 2
- 230000002401 inhibitory effect Effects 0.000 claims description 2
- 239000000314 lubricant Substances 0.000 claims description 2
- 239000006082 mold release agent Substances 0.000 claims description 2
- 150000002825 nitriles Chemical class 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- 229920003986 novolac Polymers 0.000 claims description 2
- 239000002667 nucleating agent Substances 0.000 claims description 2
- 229920001568 phenolic resin Polymers 0.000 claims description 2
- 239000005011 phenolic resin Substances 0.000 claims description 2
- 239000000049 pigment Substances 0.000 claims description 2
- 229920000647 polyepoxide Polymers 0.000 claims description 2
- 229920000570 polyether Polymers 0.000 claims description 2
- 229920006380 polyphenylene oxide Polymers 0.000 claims description 2
- 238000012545 processing Methods 0.000 claims description 2
- 230000003014 reinforcing effect Effects 0.000 claims description 2
- 239000010703 silicon Substances 0.000 claims description 2
- 229910052710 silicon Inorganic materials 0.000 claims description 2
- 229920002379 silicone rubber Polymers 0.000 claims description 2
- 239000000779 smoke Substances 0.000 claims description 2
- 150000003464 sulfur compounds Chemical class 0.000 claims description 2
- 150000003568 thioethers Chemical class 0.000 claims description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 2
- 229920002554 vinyl polymer Polymers 0.000 claims description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 2
- 239000005062 Polybutadiene Substances 0.000 claims 1
- 239000004734 Polyphenylene sulfide Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 239000012752 auxiliary agent Substances 0.000 claims 1
- 150000008298 phosphoramidates Chemical class 0.000 claims 1
- 229920000069 polyphenylene sulfide Polymers 0.000 claims 1
- 239000003755 preservative agent Substances 0.000 claims 1
- 239000011814 protection agent Substances 0.000 claims 1
- 239000003223 protective agent Substances 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 20
- 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 19
- 239000000839 emulsion Substances 0.000 description 14
- 239000003063 flame retardant Substances 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 229940106691 bisphenol a Drugs 0.000 description 9
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 9
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 239000000243 solution Substances 0.000 description 6
- 239000004594 Masterbatch (MB) Substances 0.000 description 5
- 239000003431 cross linking reagent Substances 0.000 description 5
- 230000010339 dilation Effects 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 150000003018 phosphorus compounds Chemical class 0.000 description 5
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 5
- 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 4
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- 238000000071 blow moulding Methods 0.000 description 4
- 238000001125 extrusion Methods 0.000 description 4
- 238000004898 kneading Methods 0.000 description 4
- 125000005375 organosiloxane group Chemical group 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 229920000638 styrene acrylonitrile Polymers 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 229920006362 Teflon® Polymers 0.000 description 3
- 239000002216 antistatic agent Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 238000010559 graft polymerization reaction Methods 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 3
- 229920001169 thermoplastic Polymers 0.000 description 3
- 239000004416 thermosoftening plastic Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- BSWWXRFVMJHFBN-UHFFFAOYSA-N 2,4,6-tribromophenol Chemical compound OC1=C(Br)C=C(Br)C=C1Br BSWWXRFVMJHFBN-UHFFFAOYSA-N 0.000 description 2
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000004809 Teflon Substances 0.000 description 2
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 125000001118 alkylidene group Chemical group 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 125000005587 carbonate group Chemical group 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000005227 gel permeation chromatography Methods 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- 125000004464 hydroxyphenyl group Chemical group 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 2
- 239000004810 polytetrafluoroethylene Substances 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- GRJISGHXMUQUMC-UHFFFAOYSA-N silyl prop-2-enoate Chemical compound [SiH3]OC(=O)C=C GRJISGHXMUQUMC-UHFFFAOYSA-N 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- KOMNUTZXSVSERR-UHFFFAOYSA-N 1,3,5-tris(prop-2-enyl)-1,3,5-triazinane-2,4,6-trione Chemical compound C=CCN1C(=O)N(CC=C)C(=O)N(CC=C)C1=O KOMNUTZXSVSERR-UHFFFAOYSA-N 0.000 description 1
- VDYWHVQKENANGY-UHFFFAOYSA-N 1,3-Butyleneglycol dimethacrylate Chemical compound CC(=C)C(=O)OC(C)CCOC(=O)C(C)=C VDYWHVQKENANGY-UHFFFAOYSA-N 0.000 description 1
- HKHJUFBJPODHRI-UHFFFAOYSA-N 1-[diethoxy(methyl)silyl]propyl 2-methylprop-2-enoate Chemical compound CCO[Si](C)(OCC)C(CC)OC(=O)C(C)=C HKHJUFBJPODHRI-UHFFFAOYSA-N 0.000 description 1
- UTHGLXKXKHGCFV-UHFFFAOYSA-N 1-[diethyl(propyl)silyl]oxyethyl 2-methylprop-2-enoate Chemical compound CCC[Si](CC)(CC)OC(C)OC(=O)C(C)=C UTHGLXKXKHGCFV-UHFFFAOYSA-N 0.000 description 1
- ZSRUHMKSVQKVEJ-UHFFFAOYSA-N 1-[methoxy(dimethyl)silyl]propyl 2-methylprop-2-enoate Chemical compound CO[Si](C)(C)C(CC)OC(=O)C(C)=C ZSRUHMKSVQKVEJ-UHFFFAOYSA-N 0.000 description 1
- RMSGQZDGSZOJMU-UHFFFAOYSA-N 1-butyl-2-phenylbenzene Chemical group CCCCC1=CC=CC=C1C1=CC=CC=C1 RMSGQZDGSZOJMU-UHFFFAOYSA-N 0.000 description 1
- KTZVZZJJVJQZHV-UHFFFAOYSA-N 1-chloro-4-ethenylbenzene Chemical compound ClC1=CC=C(C=C)C=C1 KTZVZZJJVJQZHV-UHFFFAOYSA-N 0.000 description 1
- HIDBROSJWZYGSZ-UHFFFAOYSA-N 1-phenylpyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1=CC=CC=C1 HIDBROSJWZYGSZ-UHFFFAOYSA-N 0.000 description 1
- NLPBRTBBFUOESW-UHFFFAOYSA-N 1-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)C(CC)OC(=O)C(C)=C NLPBRTBBFUOESW-UHFFFAOYSA-N 0.000 description 1
- YIYBRXKMQFDHSM-UHFFFAOYSA-N 2,2'-Dihydroxybenzophenone Chemical class OC1=CC=CC=C1C(=O)C1=CC=CC=C1O YIYBRXKMQFDHSM-UHFFFAOYSA-N 0.000 description 1
- XXKHDSGLCLCFSC-UHFFFAOYSA-N 2,3-diphenylphenol Chemical compound C=1C=CC=CC=1C=1C(O)=CC=CC=1C1=CC=CC=C1 XXKHDSGLCLCFSC-UHFFFAOYSA-N 0.000 description 1
- VMAWODUEPLAHOE-UHFFFAOYSA-N 2,4,6,8-tetrakis(ethenyl)-2,4,6,8-tetramethyl-1,3,5,7,2,4,6,8-tetraoxatetrasilocane Chemical compound C=C[Si]1(C)O[Si](C)(C=C)O[Si](C)(C=C)O[Si](C)(C=C)O1 VMAWODUEPLAHOE-UHFFFAOYSA-N 0.000 description 1
- IRVZFACCNZRHSJ-UHFFFAOYSA-N 2,4,6,8-tetramethyl-2,4,6,8-tetraphenyl-1,3,5,7,2,4,6,8-tetraoxatetrasilocane Chemical compound O1[Si](C)(C=2C=CC=CC=2)O[Si](C)(C=2C=CC=CC=2)O[Si](C)(C=2C=CC=CC=2)O[Si]1(C)C1=CC=CC=C1 IRVZFACCNZRHSJ-UHFFFAOYSA-N 0.000 description 1
- BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 description 1
- VXHYVVAUHMGCEX-UHFFFAOYSA-N 2-(2-hydroxyphenoxy)phenol Chemical class OC1=CC=CC=C1OC1=CC=CC=C1O VXHYVVAUHMGCEX-UHFFFAOYSA-N 0.000 description 1
- XSVZEASGNTZBRQ-UHFFFAOYSA-N 2-(2-hydroxyphenyl)sulfinylphenol Chemical class OC1=CC=CC=C1S(=O)C1=CC=CC=C1O XSVZEASGNTZBRQ-UHFFFAOYSA-N 0.000 description 1
- QUWAJPZDCZDTJS-UHFFFAOYSA-N 2-(2-hydroxyphenyl)sulfonylphenol Chemical class OC1=CC=CC=C1S(=O)(=O)C1=CC=CC=C1O QUWAJPZDCZDTJS-UHFFFAOYSA-N 0.000 description 1
- JJBFVQSGPLGDNX-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)propyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)COC(=O)C(C)=C JJBFVQSGPLGDNX-UHFFFAOYSA-N 0.000 description 1
- KAIRTVANLJFYQS-UHFFFAOYSA-N 2-(3,5-dimethylheptyl)phenol Chemical compound CCC(C)CC(C)CCC1=CC=CC=C1O KAIRTVANLJFYQS-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- HOLOIDMYVKIMCS-UHFFFAOYSA-N 2-[dimethoxy(methyl)silyl]ethyl 2-methylprop-2-enoate Chemical compound CO[Si](C)(OC)CCOC(=O)C(C)=C HOLOIDMYVKIMCS-UHFFFAOYSA-N 0.000 description 1
- XBQRPFBBTWXIFI-UHFFFAOYSA-N 2-chloro-4-[2-(3-chloro-4-hydroxyphenyl)propan-2-yl]phenol Chemical compound C=1C=C(O)C(Cl)=CC=1C(C)(C)C1=CC=C(O)C(Cl)=C1 XBQRPFBBTWXIFI-UHFFFAOYSA-N 0.000 description 1
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-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
- XOJWAAUYNWGQAU-UHFFFAOYSA-N 4-(2-methylprop-2-enoyloxy)butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCOC(=O)C(C)=C XOJWAAUYNWGQAU-UHFFFAOYSA-N 0.000 description 1
- CUAUDSWILJWDOD-UHFFFAOYSA-N 4-(3,5-dimethylheptyl)phenol Chemical compound CCC(C)CC(C)CCC1=CC=C(O)C=C1 CUAUDSWILJWDOD-UHFFFAOYSA-N 0.000 description 1
- HVXRCAWUNAOCTA-UHFFFAOYSA-N 4-(6-methylheptyl)phenol Chemical compound CC(C)CCCCCC1=CC=C(O)C=C1 HVXRCAWUNAOCTA-UHFFFAOYSA-N 0.000 description 1
- KJWMCPYEODZESQ-UHFFFAOYSA-N 4-Dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=C(O)C=C1 KJWMCPYEODZESQ-UHFFFAOYSA-N 0.000 description 1
- UMPGNGRIGSEMTC-UHFFFAOYSA-N 4-[1-(4-hydroxyphenyl)-3,3,5-trimethylcyclohexyl]phenol Chemical compound C1C(C)CC(C)(C)CC1(C=1C=CC(O)=CC=1)C1=CC=C(O)C=C1 UMPGNGRIGSEMTC-UHFFFAOYSA-N 0.000 description 1
- KSYGTCNPCHQRKM-UHFFFAOYSA-N 4-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 KSYGTCNPCHQRKM-UHFFFAOYSA-N 0.000 description 1
- NIRYBKWMEWFDPM-UHFFFAOYSA-N 4-[3-(4-hydroxyphenyl)-3-methylbutyl]phenol Chemical compound C=1C=C(O)C=CC=1C(C)(C)CCC1=CC=C(O)C=C1 NIRYBKWMEWFDPM-UHFFFAOYSA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
- WXNZTHHGJRFXKQ-UHFFFAOYSA-N 4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1 WXNZTHHGJRFXKQ-UHFFFAOYSA-N 0.000 description 1
- QHPQWRBYOIRBIT-UHFFFAOYSA-N 4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C=C1 QHPQWRBYOIRBIT-UHFFFAOYSA-N 0.000 description 1
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
-
- 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
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/10—Process efficiency
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W10/00—Technologies for wastewater treatment
- Y02W10/30—Wastewater or sewage treatment systems using renewable energies
- Y02W10/37—Wastewater or sewage treatment systems using renewable energies using solar energy
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Automation & Control Theory (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Distillation Of Fermentation Liquor, Processing Of Alcohols, Vinegar And Beer (AREA)
- Vaporization, Distillation, Condensation, Sublimation, And Cold Traps (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2002156316 DE10256316A1 (de) | 2002-12-03 | 2002-12-03 | Polycarbonat-Formmassen |
| PCT/EP2003/012994 WO2004050755A1 (de) | 2002-12-03 | 2003-11-20 | Polycarbonat-formmassen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MXPA05005974A true MXPA05005974A (es) | 2005-08-18 |
Family
ID=32335914
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MXPA05005974A MXPA05005974A (es) | 2002-12-03 | 2003-11-20 | Masas del moldeo de policarbonato. |
Country Status (13)
| Country | Link |
|---|---|
| US (2) | US20040108196A1 (enExample) |
| EP (1) | EP1569995B1 (enExample) |
| JP (1) | JP4398871B2 (enExample) |
| KR (1) | KR100986016B1 (enExample) |
| CN (1) | CN100582150C (enExample) |
| AU (1) | AU2003298126A1 (enExample) |
| BR (1) | BR0316984B1 (enExample) |
| CA (1) | CA2507928C (enExample) |
| DE (2) | DE10256316A1 (enExample) |
| ES (1) | ES2294362T3 (enExample) |
| MX (1) | MXPA05005974A (enExample) |
| TW (1) | TWI329121B (enExample) |
| WO (1) | WO2004050755A1 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10036057A1 (de) * | 2000-07-25 | 2002-02-07 | Bayer Ag | Flammwidrige Polycarbonat-Zusammensetzungen |
| WO2007001130A1 (en) * | 2005-06-29 | 2007-01-04 | Cheil Industries Inc. | Polycarbonate resin composition having good chemical resistance and flowability |
| US7446144B2 (en) * | 2005-09-14 | 2008-11-04 | Bayer Materialscience Llc | Thermoplastic molding composition and articles thermoformed therefrom |
| KR100838451B1 (ko) * | 2005-12-30 | 2008-06-16 | 제일모직주식회사 | 내열도가 높고, 내충격성이 우수한 난연성 폴리카보네이트수지 조성물 |
| DE102006012990A1 (de) * | 2006-03-22 | 2007-09-27 | Bayer Materialscience Ag | Flammgeschützte schlagzähmodifizierte Polycarbonat-Zusammensetzungen |
| JP5398843B2 (ja) * | 2008-12-08 | 2014-01-29 | 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 | 難燃性ポリカーボネート組成物、その製造方法、およびその物品 |
| TWI418883B (zh) * | 2010-03-17 | 2013-12-11 | Au Optronics Corp | 修補方法以及主動元件陣列基板 |
| US8218291B2 (en) * | 2010-03-31 | 2012-07-10 | General Electric Company | Monomers for preparing polycarbonate resins, methods of preparing the monomers, polycarbonate resins prepared with the monomers, and capacitors comprising the polycarbonate resins |
| KR101499246B1 (ko) * | 2012-08-06 | 2015-03-05 | 제일모직주식회사 | 분지형 폴리카보네이트 수지 및 그 제조방법 |
| KR102316905B1 (ko) | 2017-03-10 | 2021-10-25 | 어드밴식스 레진즈 앤드 케미컬즈 엘엘씨 | 개선된 가공성 및 특성을 위한 pa6/66 공중합체 베이스 수지의 와이어 및 케이블 피복 조성물 |
| CN112546659B (zh) * | 2020-12-08 | 2022-02-15 | 云南临沧鑫圆锗业股份有限公司 | 一种四氟化锗的提纯装置及方法 |
Family Cites Families (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3946495A (en) * | 1973-12-19 | 1976-03-30 | Asriel Osdor | Method and apparatus for drying moisture-containing solids particularly domestic refuse and sludge cakes |
| JPS50109247A (ja) | 1974-02-04 | 1975-08-28 | Sumitomo Chemical Co | Netsukasoseijushisoseibutsu |
| US4185009A (en) * | 1975-01-03 | 1980-01-22 | Bayer Aktiengesellschaft | Branched, high-molecular weight thermoplastic polycarbonates |
| JPS5661446A (en) * | 1979-10-24 | 1981-05-26 | Ajinomoto Co Inc | Stabilizer for halogen-containing resin |
| US4358346A (en) * | 1981-05-06 | 1982-11-09 | The Foxboro Company | Control of alcohol distillation |
| JPS5898354A (ja) | 1981-12-07 | 1983-06-11 | Sumitomo Naugatuck Co Ltd | 熱可塑性樹脂組成物 |
| DE3149812A1 (de) | 1981-12-16 | 1983-07-21 | Basf Ag, 6700 Ludwigshafen | Thermoplastische formmassen |
| JPH0796110B2 (ja) * | 1986-04-04 | 1995-10-18 | コニカ株式会社 | 写真処理廃液処理方法及びその装置 |
| US5068285A (en) * | 1989-03-08 | 1991-11-26 | The Dow Chemical Company | Molding compositions with acrylonitrile-styrene-acrylate rubber copolymers |
| US5087663A (en) * | 1989-03-08 | 1992-02-11 | The Dow Chemical Company | Molding compositions with methyl (meth)acrylate-butadiene-styrene graft copolymers |
| DE3924493A1 (de) * | 1989-07-25 | 1991-01-31 | Bayer Ag | Flammwidrige mischungen |
| DE69231876T2 (de) | 1991-01-24 | 2001-10-18 | Idemitsu Petrochemical Co., Ltd. | Polymermischung, die ein verzweigtes Polycarbonat enthält |
| US5314949A (en) * | 1991-01-24 | 1994-05-24 | Idemitsu Petrochemical Co., Ltd. | Polycarbonate resin composition |
| US5258432A (en) * | 1992-03-10 | 1993-11-02 | The Dow Chemical Company | Ignition resistant polycarbonate blends |
| JPH08319406A (ja) * | 1995-05-26 | 1996-12-03 | Kanegafuchi Chem Ind Co Ltd | 難燃性樹脂組成物 |
| TWI234574B (en) * | 1997-05-06 | 2005-06-21 | Idemitsu Kosan Co | Battery pack obtained from a flame-retardant polycarbonate resin composition |
| DE19801198A1 (de) * | 1998-01-15 | 1999-07-22 | Bayer Ag | Flammwidrige Polycarbonat-ABS-Formmassen |
| EP1076675A1 (en) | 1998-05-01 | 2001-02-21 | General Electric Company | Flame retardant polycarbonate/rubber-modified graft copolymer resin blends having a low fluorine content |
| DE69805447T2 (de) * | 1998-06-30 | 2003-01-16 | Centre De Recherche Industrielle Du Quebec, Ste-Foy | Verfahren zur biologischen abwasser- und abgasreinigung und biofilter dafür |
| CA2346711C (en) * | 1998-10-20 | 2003-12-30 | Kevin Lee Kott | Laundry detergents comprising modified alkylbenzene sulfonates |
| JP4627833B2 (ja) * | 2000-02-10 | 2011-02-09 | 旭化成ケミカルズ株式会社 | ポリカーボネート組成物 |
| AU2001287732A1 (en) * | 2000-09-26 | 2002-04-08 | Bayer Aktiengesellschaft | Copolycarbonate-based composition |
| DE10119681A1 (de) * | 2001-04-20 | 2002-10-24 | Bayer Ag | Schlagzähmodifizierte Blends aus Polyethylenenterephthalat und mindestens einem auf Dihydtoxydlarylcyclohexan basierenden Polycarbonat |
| DE10162747A1 (de) * | 2001-12-20 | 2003-07-03 | Bayer Ag | Extrudierbare Polycarbonat-Formmassen |
-
2002
- 2002-12-03 DE DE2002156316 patent/DE10256316A1/de not_active Withdrawn
-
2003
- 2003-11-20 EP EP20030795829 patent/EP1569995B1/de not_active Expired - Lifetime
- 2003-11-20 AU AU2003298126A patent/AU2003298126A1/en not_active Abandoned
- 2003-11-20 CN CN200380104975A patent/CN100582150C/zh not_active Expired - Fee Related
- 2003-11-20 CA CA 2507928 patent/CA2507928C/en not_active Expired - Fee Related
- 2003-11-20 BR BR0316984A patent/BR0316984B1/pt not_active IP Right Cessation
- 2003-11-20 ES ES03795829T patent/ES2294362T3/es not_active Expired - Lifetime
- 2003-11-20 JP JP2004556161A patent/JP4398871B2/ja not_active Expired - Fee Related
- 2003-11-20 MX MXPA05005974A patent/MXPA05005974A/es active IP Right Grant
- 2003-11-20 DE DE50308665T patent/DE50308665D1/de not_active Expired - Lifetime
- 2003-11-20 WO PCT/EP2003/012994 patent/WO2004050755A1/de not_active Ceased
- 2003-11-20 KR KR20057009981A patent/KR100986016B1/ko not_active Expired - Fee Related
- 2003-12-01 US US10/726,210 patent/US20040108196A1/en not_active Abandoned
- 2003-12-01 US US10/725,210 patent/US7186767B2/en not_active Expired - Lifetime
- 2003-12-02 TW TW92133763A patent/TWI329121B/zh not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| EP1569995A1 (de) | 2005-09-07 |
| KR20050085295A (ko) | 2005-08-29 |
| US20040106731A1 (en) | 2004-06-03 |
| JP4398871B2 (ja) | 2010-01-13 |
| US20040108196A1 (en) | 2004-06-10 |
| WO2004050755A1 (de) | 2004-06-17 |
| DE10256316A1 (de) | 2004-06-24 |
| US7186767B2 (en) | 2007-03-06 |
| DE50308665D1 (de) | 2008-01-03 |
| BR0316984A (pt) | 2005-10-25 |
| BR0316984B1 (pt) | 2013-10-22 |
| EP1569995B1 (de) | 2007-11-21 |
| AU2003298126A1 (en) | 2004-06-23 |
| CN1720290A (zh) | 2006-01-11 |
| TWI329121B (en) | 2010-08-21 |
| KR100986016B1 (ko) | 2010-10-06 |
| ES2294362T3 (es) | 2008-04-01 |
| JP2006509065A (ja) | 2006-03-16 |
| TW200426179A (en) | 2004-12-01 |
| CA2507928C (en) | 2012-05-29 |
| CN100582150C (zh) | 2010-01-20 |
| CA2507928A1 (en) | 2004-06-17 |
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Legal Events
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| FG | Grant or registration |