JP2004536193A5 - - Google Patents

Info

Publication number

JP2004536193A5

JP2004536193A5 JP2003514052A JP2003514052A JP2004536193A5 JP 2004536193 A5 JP2004536193 A5 JP 2004536193A5 JP 2003514052 A JP2003514052 A JP 2003514052A JP 2003514052 A JP2003514052 A JP 2003514052A JP 2004536193 A5 JP2004536193 A5 JP 2004536193A5

Authority

JP

Japan

Prior art keywords

composition

acid

metal salt

polysiloxane

formula

Prior art date

2002-06-26

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.)

Ceased

Links

• Espacenet
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• 239000000203 mixture Substances 0.000 claims 17
• -1 polysiloxane units Polymers 0.000 claims 14
• 229920001296 polysiloxane Polymers 0.000 claims 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 claims 5
• 229920001400 block copolymer Polymers 0.000 claims 5
• 239000003063 flame retardant Substances 0.000 claims 5
• 239000007848 Bronsted acid Substances 0.000 claims 4
• 239000002253 acid Substances 0.000 claims 4
• 229910052783 alkali metal Inorganic materials 0.000 claims 4
• 229910052784 alkaline earth metal Inorganic materials 0.000 claims 4
• 125000001183 hydrocarbyl group Chemical group 0.000 claims 4
• 238000000034 method Methods 0.000 claims 4
• ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 3
• 239000006085 branching agent Substances 0.000 claims 3
• 239000011541 reaction mixture Substances 0.000 claims 3
• 229920001169 thermoplastic Polymers 0.000 claims 3
• 239000004416 thermosoftening plastic Substances 0.000 claims 3
• 239000003963 antioxidant agent Substances 0.000 claims 2
• 230000003078 antioxidant effect Effects 0.000 claims 2
• 239000002216 antistatic agent Substances 0.000 claims 2
• QMKYBPDZANOJGF-UHFFFAOYSA-N benzene-1,3,5-tricarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=CC(C(O)=O)=C1 QMKYBPDZANOJGF-UHFFFAOYSA-N 0.000 claims 2
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 2
• 150000001244 carboxylic acid anhydrides Chemical group 0.000 claims 2
• 150000001732 carboxylic acid derivatives Chemical group 0.000 claims 2
• 239000003795 chemical substances by application Substances 0.000 claims 2
• 239000004088 foaming agent Substances 0.000 claims 2
• 125000000524 functional group Chemical group 0.000 claims 2
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
• 239000004611 light stabiliser Substances 0.000 claims 2
• 150000002894 organic compounds Chemical class 0.000 claims 2
• 239000004014 plasticizer Substances 0.000 claims 2
• 239000011347 resin Substances 0.000 claims 2
• 229920005989 resin Polymers 0.000 claims 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 claims 2
• UITKHKNFVCYWNG-UHFFFAOYSA-N 4-(3,4-dicarboxybenzoyl)phthalic acid Chemical compound C1=C(C(O)=O)C(C(=O)O)=CC=C1C(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 UITKHKNFVCYWNG-UHFFFAOYSA-N 0.000 claims 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 claims 1
• BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims 1
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
• 239000008346 aqueous phase Substances 0.000 claims 1
• CJPIDIRJSIUWRJ-UHFFFAOYSA-N benzene-1,2,4-tricarbonyl chloride Chemical compound ClC(=O)C1=CC=C(C(Cl)=O)C(C(Cl)=O)=C1 CJPIDIRJSIUWRJ-UHFFFAOYSA-N 0.000 claims 1
• 239000003054 catalyst Substances 0.000 claims 1
• 230000003197 catalytic effect Effects 0.000 claims 1
• 125000000753 cycloalkyl group Chemical group 0.000 claims 1
• 150000002009 diols Chemical class 0.000 claims 1
• 239000012760 heat stabilizer Substances 0.000 claims 1
• 229910052739 hydrogen Inorganic materials 0.000 claims 1
• 239000001257 hydrogen Substances 0.000 claims 1
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
• 239000000463 material Substances 0.000 claims 1
• 239000012074 organic phase Substances 0.000 claims 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 claims 1
• 239000012071 phase Substances 0.000 claims 1
• 229920000515 polycarbonate Polymers 0.000 claims 1
• 239000004417 polycarbonate Substances 0.000 claims 1
• 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 claims 1
• 239000002243 precursor Substances 0.000 claims 1
• 150000003839 salts Chemical class 0.000 claims 1
• 238000003756 stirring Methods 0.000 claims 1
• 239000003017 thermal stabilizer Substances 0.000 claims 1
• SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 claims 1
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1