JPWO2022260076A5 - - Google Patents

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Publication number

JPWO2022260076A5

JPWO2022260076A5 JP2023527891A JP2023527891A JPWO2022260076A5 JP WO2022260076 A5 JPWO2022260076 A5 JP WO2022260076A5 JP 2023527891 A JP2023527891 A JP 2023527891A JP 2023527891 A JP2023527891 A JP 2023527891A JP WO2022260076 A5 JPWO2022260076 A5 JP WO2022260076A5

Authority

JP

Japan

Prior art keywords

group

carbon atoms

polycarbonate resin

resin composition

composition according

Prior art date

2022-06-08

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

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• 125000004432 carbon atom Chemical group C* 0.000 claims 33
• 229920005668 polycarbonate resin Polymers 0.000 claims 25
• 239000004431 polycarbonate resin Substances 0.000 claims 25
• 239000000203 mixture Substances 0.000 claims 21
• 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 8
• 239000003063 flame retardant Substances 0.000 claims 8
• 229920001577 copolymer Polymers 0.000 claims 7
• 125000002947 alkylene group Chemical group 0.000 claims 5
• 125000000732 arylene group Chemical group 0.000 claims 5
• 229920000515 polycarbonate Polymers 0.000 claims 5
• 239000004417 polycarbonate Substances 0.000 claims 5
• 125000000217 alkyl group Chemical group 0.000 claims 4
• 125000005843 halogen group Chemical group 0.000 claims 4
• 125000001931 aliphatic group Chemical group 0.000 claims 3
• 125000003118 aryl group Chemical group 0.000 claims 3
• -1 diisocyanate compound Chemical class 0.000 claims 3
• OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims 2
• 125000003545 alkoxy group Chemical group 0.000 claims 2
• 125000001118 alkylidene group Chemical group 0.000 claims 2
• 125000004429 atom Chemical group 0.000 claims 2
• 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 2
• WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims 2
• 238000005259 measurement Methods 0.000 claims 2
• 238000000465 moulding Methods 0.000 claims 2
• 229910052757 nitrogen Inorganic materials 0.000 claims 2
• 125000004433 nitrogen atom Chemical group N* 0.000 claims 2
• 125000004430 oxygen atom Chemical group O* 0.000 claims 2
• 229910052717 sulfur Inorganic materials 0.000 claims 2
• 125000004434 sulfur atom Chemical group 0.000 claims 2
• 238000009864 tensile test Methods 0.000 claims 2
• 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 claims 2
• RSJKGSCJYJTIGS-UHFFFAOYSA-N undecane Chemical compound CCCCCCCCCCC RSJKGSCJYJTIGS-UHFFFAOYSA-N 0.000 claims 2
• DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 claims 1
• YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 claims 1
• YMTYZTXUZLQUSF-UHFFFAOYSA-N 3,3'-Dimethylbisphenol A Chemical compound C1=C(O)C(C)=CC(C(C)(C)C=2C=C(C)C(O)=CC=2)=C1 YMTYZTXUZLQUSF-UHFFFAOYSA-N 0.000 claims 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 claims 1
• GYLZMVYMSPSPDA-UHFFFAOYSA-N 4-[1-(4-hydroxyphenyl)-3-methylcyclohexyl]phenol Chemical compound C1C(C)CCCC1(C=1C=CC(O)=CC=1)C1=CC=C(O)C=C1 GYLZMVYMSPSPDA-UHFFFAOYSA-N 0.000 claims 1
• 125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
• XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims 1
• KLDXJTOLSGUMSJ-JGWLITMVSA-N Isosorbide Chemical compound O[C@@H]1CO[C@@H]2[C@@H](O)CO[C@@H]21 KLDXJTOLSGUMSJ-JGWLITMVSA-N 0.000 claims 1
• RNYJMMUGZVKTNC-UHFFFAOYSA-N OC1=CC=C(C=C1)C1(C=CCCCCCCCCC1)C1=CC=C(C=C1)O Chemical compound OC1=CC=C(C=C1)C1(C=CCCCCCCCCC1)C1=CC=C(C=C1)O RNYJMMUGZVKTNC-UHFFFAOYSA-N 0.000 claims 1
• OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 1
• YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 claims 1
• 125000002723 alicyclic group Chemical group 0.000 claims 1
• 125000002877 alkyl aryl group Chemical group 0.000 claims 1
• 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims 1
• 150000001875 compounds Chemical class 0.000 claims 1
• 125000004122 cyclic group Chemical group 0.000 claims 1
• 125000002993 cycloalkylene group Chemical group 0.000 claims 1
• 150000002009 diols Chemical class 0.000 claims 1
• 150000004820 halides Chemical class 0.000 claims 1
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
• 229960002479 isosorbide Drugs 0.000 claims 1
• 239000000155 melt Substances 0.000 claims 1
• 239000002184 metal Substances 0.000 claims 1
• 238000000034 method Methods 0.000 claims 1
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
• 239000000178 monomer Substances 0.000 claims 1
• OTLDLKLSNZMTTA-UHFFFAOYSA-N octahydro-1h-4,7-methanoindene-1,5-diyldimethanol Chemical compound C1C2C3C(CO)CCC3C1C(CO)C2 OTLDLKLSNZMTTA-UHFFFAOYSA-N 0.000 claims 1
• 229910052698 phosphorus Inorganic materials 0.000 claims 1
• 239000011574 phosphorus Substances 0.000 claims 1
• 238000006116 polymerization reaction Methods 0.000 claims 1
• 229920000166 polytrimethylene carbonate Polymers 0.000 claims 1
• 239000011342 resin composition Substances 0.000 claims 1
• 150000003839 salts Chemical class 0.000 claims 1
• 125000001424 substituent group Chemical group 0.000 claims 1