JPWO2020153329A1 - 脂肪族ポリカーボネート - Google Patents
脂肪族ポリカーボネート Download PDFInfo
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- JPWO2020153329A1 JPWO2020153329A1 JP2020568147A JP2020568147A JPWO2020153329A1 JP WO2020153329 A1 JPWO2020153329 A1 JP WO2020153329A1 JP 2020568147 A JP2020568147 A JP 2020568147A JP 2020568147 A JP2020568147 A JP 2020568147A JP WO2020153329 A1 JPWO2020153329 A1 JP WO2020153329A1
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- aliphatic polycarbonate
- formula
- substituted
- aliphatic
- Prior art date
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- 125000001931 aliphatic group Chemical group 0.000 title claims abstract description 191
- 239000004417 polycarbonate Substances 0.000 title claims abstract description 184
- 229920000515 polycarbonate Polymers 0.000 title claims abstract description 184
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 39
- 125000003118 aryl group Chemical group 0.000 claims abstract description 34
- 125000001424 substituent group Chemical group 0.000 claims abstract description 32
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 29
- 125000005842 heteroatom Chemical group 0.000 claims abstract description 13
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 12
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 11
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 7
- YZCKVEUIGOORGS-IGMARMGPSA-N Protium Chemical compound [1H] YZCKVEUIGOORGS-IGMARMGPSA-N 0.000 claims abstract description 5
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims abstract description 4
- 239000000203 mixture Substances 0.000 claims description 81
- 239000003431 cross linking reagent Substances 0.000 claims description 34
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 29
- 230000001070 adhesive effect Effects 0.000 claims description 10
- 239000011230 binding agent Substances 0.000 claims description 10
- 239000000853 adhesive Substances 0.000 claims description 9
- 239000002270 dispersing agent Substances 0.000 claims description 9
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- 239000008199 coating composition Substances 0.000 claims description 7
- 229910052757 nitrogen Inorganic materials 0.000 claims description 7
- 125000004429 atom Chemical group 0.000 claims description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- 125000004434 sulfur atom Chemical group 0.000 claims description 3
- 238000000034 method Methods 0.000 abstract description 27
- 125000000524 functional group Chemical group 0.000 abstract description 5
- 238000000197 pyrolysis Methods 0.000 abstract description 3
- 125000002723 alicyclic group Chemical group 0.000 abstract 1
- -1 polyethylene Polymers 0.000 description 49
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 45
- 239000003054 catalyst Substances 0.000 description 44
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 39
- 238000006243 chemical reaction Methods 0.000 description 39
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 37
- 239000002904 solvent Substances 0.000 description 35
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 34
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 34
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 30
- 239000002243 precursor Substances 0.000 description 27
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 24
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 24
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 24
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 21
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 21
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 20
- 239000001569 carbon dioxide Substances 0.000 description 17
- 229910002092 carbon dioxide Inorganic materials 0.000 description 17
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 16
- 125000003545 alkoxy group Chemical group 0.000 description 15
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 15
- 150000002118 epoxides Chemical class 0.000 description 15
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 14
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 14
- 238000011156 evaluation Methods 0.000 description 14
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 14
- 238000006116 polymerization reaction Methods 0.000 description 14
- 239000000243 solution Substances 0.000 description 14
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 12
- 125000004423 acyloxy group Chemical group 0.000 description 12
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 12
- 238000004519 manufacturing process Methods 0.000 description 12
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 12
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 11
- 229910052751 metal Inorganic materials 0.000 description 11
- 239000002184 metal Substances 0.000 description 11
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 11
- 238000005160 1H NMR spectroscopy Methods 0.000 description 10
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 10
- 239000000654 additive Substances 0.000 description 10
- 239000000178 monomer Substances 0.000 description 10
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 10
- 239000011701 zinc Substances 0.000 description 10
- 229910052725 zinc Inorganic materials 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- 125000003277 amino group Chemical group 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 8
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 8
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 8
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 8
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 8
- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 description 8
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 description 8
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 8
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 description 8
- 229940011051 isopropyl acetate Drugs 0.000 description 8
- GWYFCOCPABKNJV-UHFFFAOYSA-N isovaleric acid Chemical compound CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- UODXCYZDMHPIJE-UHFFFAOYSA-N menthanol Chemical compound CC1CCC(C(C)(C)O)CC1 UODXCYZDMHPIJE-UHFFFAOYSA-N 0.000 description 8
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 8
- 125000001624 naphthyl group Chemical group 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- 239000008096 xylene Substances 0.000 description 8
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 7
- 230000000996 additive effect Effects 0.000 description 7
- JRPBQTZRNDNNOP-UHFFFAOYSA-N barium titanate Chemical compound [Ba+2].[Ba+2].[O-][Ti]([O-])([O-])[O-] JRPBQTZRNDNNOP-UHFFFAOYSA-N 0.000 description 7
- 229910002113 barium titanate Inorganic materials 0.000 description 7
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 7
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 7
- 239000000049 pigment Substances 0.000 description 7
- 229920000642 polymer Polymers 0.000 description 7
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 7
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 6
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 6
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 6
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 6
- 125000001231 benzoyloxy group Chemical group C(C1=CC=CC=C1)(=O)O* 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 229910052801 chlorine Inorganic materials 0.000 description 6
- 125000001309 chloro group Chemical group Cl* 0.000 description 6
- 238000010511 deprotection reaction Methods 0.000 description 6
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 6
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 6
- 229910052731 fluorine Inorganic materials 0.000 description 6
- 125000001153 fluoro group Chemical group F* 0.000 description 6
- 125000005843 halogen group Chemical group 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 229910052740 iodine Inorganic materials 0.000 description 6
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 6
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 6
- 238000005259 measurement Methods 0.000 description 6
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 6
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 6
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 6
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 6
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 6
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 6
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 6
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 6
- 238000004448 titration Methods 0.000 description 6
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 description 5
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 5
- 229930003836 cresol Natural products 0.000 description 5
- 238000009826 distribution Methods 0.000 description 5
- 239000011521 glass Substances 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 150000003254 radicals Chemical class 0.000 description 5
- 239000000758 substrate Substances 0.000 description 5
- 238000005979 thermal decomposition reaction Methods 0.000 description 5
- 125000003396 thiol group Chemical group [H]S* 0.000 description 5
- DEUGOISHWHDTIR-UHFFFAOYSA-N (1-hydroxy-5,5-dimethylhexyl) 2-methylpropanoate Chemical compound C(C(C)C)(=O)OC(CCCC(C)(C)C)O DEUGOISHWHDTIR-UHFFFAOYSA-N 0.000 description 4
- DAFHKNAQFPVRKR-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylpropanoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)C DAFHKNAQFPVRKR-UHFFFAOYSA-N 0.000 description 4
- MZQZXSHFWDHNOW-UHFFFAOYSA-N 1-phenylpropane-1,2-diol Chemical compound CC(O)C(O)C1=CC=CC=C1 MZQZXSHFWDHNOW-UHFFFAOYSA-N 0.000 description 4
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 4
- VXQBJTKSVGFQOL-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethyl acetate Chemical compound CCCCOCCOCCOC(C)=O VXQBJTKSVGFQOL-UHFFFAOYSA-N 0.000 description 4
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 4
- HBNHCGDYYBMKJN-UHFFFAOYSA-N 2-(4-methylcyclohexyl)propan-2-yl acetate Chemical compound CC1CCC(C(C)(C)OC(C)=O)CC1 HBNHCGDYYBMKJN-UHFFFAOYSA-N 0.000 description 4
- YJTIFIMHZHDNQZ-UHFFFAOYSA-N 2-[2-(2-methylpropoxy)ethoxy]ethanol Chemical compound CC(C)COCCOCCO YJTIFIMHZHDNQZ-UHFFFAOYSA-N 0.000 description 4
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 4
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 4
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 4
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 4
- MRABAEUHTLLEML-UHFFFAOYSA-N Butyl lactate Chemical compound CCCCOC(=O)C(C)O MRABAEUHTLLEML-UHFFFAOYSA-N 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 4
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 4
- 239000002841 Lewis acid Substances 0.000 description 4
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 4
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 238000007259 addition reaction Methods 0.000 description 4
- 239000012298 atmosphere Substances 0.000 description 4
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 4
- ZFMQKOWCDKKBIF-UHFFFAOYSA-N bis(3,5-difluorophenyl)phosphane Chemical compound FC1=CC(F)=CC(PC=2C=C(F)C=C(F)C=2)=C1 ZFMQKOWCDKKBIF-UHFFFAOYSA-N 0.000 description 4
- 239000001191 butyl (2R)-2-hydroxypropanoate Substances 0.000 description 4
- 150000001721 carbon Chemical group 0.000 description 4
- 239000007810 chemical reaction solvent Substances 0.000 description 4
- 239000003426 co-catalyst Substances 0.000 description 4
- 239000010941 cobalt Substances 0.000 description 4
- 229910017052 cobalt Inorganic materials 0.000 description 4
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 4
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 4
- 239000003999 initiator Substances 0.000 description 4
- 229910010272 inorganic material Inorganic materials 0.000 description 4
- 239000011147 inorganic material Substances 0.000 description 4
- 150000007517 lewis acids Chemical class 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 238000006011 modification reaction Methods 0.000 description 4
- 238000006386 neutralization reaction Methods 0.000 description 4
- 239000012299 nitrogen atmosphere Substances 0.000 description 4
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 239000002002 slurry Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 3
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 3
- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 229910004298 SiO 2 Inorganic materials 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
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- YZERDTREOUSUHF-UHFFFAOYSA-N pentafluorobenzoic acid Chemical compound OC(=O)C1=C(F)C(F)=C(F)C(F)=C1F YZERDTREOUSUHF-UHFFFAOYSA-N 0.000 description 1
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 description 1
- 229960005235 piperonyl butoxide Drugs 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000767 polyaniline Polymers 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 229960003975 potassium Drugs 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- NTTOTNSKUYCDAV-UHFFFAOYSA-N potassium hydride Chemical compound [KH] NTTOTNSKUYCDAV-UHFFFAOYSA-N 0.000 description 1
- 229910000105 potassium hydride Inorganic materials 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 229940086066 potassium hydrogencarbonate Drugs 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- BGUWFUQJCDRPTL-UHFFFAOYSA-N pyridine-4-carbaldehyde Chemical compound O=CC1=CC=NC=C1 BGUWFUQJCDRPTL-UHFFFAOYSA-N 0.000 description 1
- 238000001226 reprecipitation Methods 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000005368 silicate glass Substances 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 229910000679 solder Inorganic materials 0.000 description 1
- 239000011973 solid acid Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 238000006557 surface reaction Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- PUGUQINMNYINPK-UHFFFAOYSA-N tert-butyl 4-(2-chloroacetyl)piperazine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCN(C(=O)CCl)CC1 PUGUQINMNYINPK-UHFFFAOYSA-N 0.000 description 1
- YANSSVVGZPNSKD-UHFFFAOYSA-N tert-butyl-dimethyl-(oxiran-2-ylmethoxy)silane Chemical compound CC(C)(C)[Si](C)(C)OCC1CO1 YANSSVVGZPNSKD-UHFFFAOYSA-N 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical class CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 1
- NHGXDBSUJJNIRV-UHFFFAOYSA-M tetrabutylammonium chloride Chemical compound [Cl-].CCCC[N+](CCCC)(CCCC)CCCC NHGXDBSUJJNIRV-UHFFFAOYSA-M 0.000 description 1
- MCZDHTKJGDCTAE-UHFFFAOYSA-M tetrabutylazanium;acetate Chemical compound CC([O-])=O.CCCC[N+](CCCC)(CCCC)CCCC MCZDHTKJGDCTAE-UHFFFAOYSA-M 0.000 description 1
- DPKBAXPHAYBPRL-UHFFFAOYSA-M tetrabutylazanium;iodide Chemical compound [I-].CCCC[N+](CCCC)(CCCC)CCCC DPKBAXPHAYBPRL-UHFFFAOYSA-M 0.000 description 1
- QHOKENWFMZXSEU-UHFFFAOYSA-N tetrabutylazanium;nitrate Chemical compound [O-][N+]([O-])=O.CCCC[N+](CCCC)(CCCC)CCCC QHOKENWFMZXSEU-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- NJRXVEJTAYWCQJ-UHFFFAOYSA-N thiomalic acid Chemical compound OC(=O)CC(S)C(O)=O NJRXVEJTAYWCQJ-UHFFFAOYSA-N 0.000 description 1
- 229940098465 tincture Drugs 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 description 1
- RXJKFRMDXUJTEX-UHFFFAOYSA-N triethylphosphine Chemical compound CCP(CC)CC RXJKFRMDXUJTEX-UHFFFAOYSA-N 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 1
- JLTRXTDYQLMHGR-UHFFFAOYSA-N trimethylaluminium Chemical compound C[Al](C)C JLTRXTDYQLMHGR-UHFFFAOYSA-N 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 239000004246 zinc acetate Substances 0.000 description 1
- HEPBQSXQJMTVFI-UHFFFAOYSA-N zinc;butane Chemical compound [Zn+2].CCC[CH2-].CCC[CH2-] HEPBQSXQJMTVFI-UHFFFAOYSA-N 0.000 description 1
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Abstract
Description
項1.
式(1):
式(1)で表される構造単位の含有量が、式(1)と式(2)の構造単位の合計量に対して、0.1モル%以上1.5モル%以下である、脂肪族ポリカーボネート。
項2.
質量平均分子量が6万以上100万以下である項1に記載の脂肪族ポリカーボネート。
項3.
式(1)のXにおいて、ヘテロ原子を含む2価の基が、酸素原子、窒素原子、及び硫黄原子からなる群より選択される少なくとも1種の原子を含む基である、項1又は2に記載の脂肪族ポリカーボネート。
項4.
式(1)のXにおいて、ヘテロ原子を含む2価の基が、式(a):
で表される基である、項1又は2に記載の脂肪族ポリカーボネート。
項5.
式(1)で表される構造単位及び式(2)で表される構造単位のみからなる、請求項1〜4のいずれかに記載の脂肪族ポリカーボネート。
項6.
項1〜5のいずれかに記載の脂肪族ポリカーボネートと架橋剤とを含む脂肪族ポリカーボネート組成物。
項7.
項1〜5のいずれかに記載の脂肪族ポリカーボネート、又は項6に記載の脂肪族ポリカーボネート組成物を用いて得られる接着剤組成物。
項8.
項1〜5のいずれかに記載の脂肪族ポリカーボネート、又は項6に記載の脂肪族ポリカーボネート組成物を含むインク組成物。
項9.
項1〜5のいずれかに記載の脂肪族ポリカーボネート、又は項6に記載の脂肪族ポリカーボネート組成物を含むコーティング用組成物。
項10.
項1〜5のいずれかに記載の脂肪族ポリカーボネート、又は項6に記載の脂肪族ポリカーボネート組成物を含む焼成用バインダー。
項11.
項1〜5のいずれかに記載の脂肪族ポリカーボネート、又は項6に記載の脂肪族ポリカーボネート組成物を含む分散剤。
で表される構造単位と、式(2):
で表される構造単位とを含む、脂肪族ポリカーボネートである。
脂肪族ポリカーボネート2.0gをテトラヒドロフラン/水=10/1(wt/wt)溶液40.0gに溶解させ、その溶液を0.1mol/L水酸化ナトリウム水溶液で中和滴定を行い、要した水酸化ナトリウム水溶液の量、空試験(脂肪族ポリカーボネートを含まない溶液を用いた測定)に要した水酸化ナトリウム水溶液の量から樹脂中の式(1)で表される構造単位の含有量を算出した。式(1)及び式(2)の構造単位のみからなる脂肪族ポリカーボネートを例として、より詳細に説明すると、式(1)、式(2)の構造単位の分子量をそれぞれF1、F2、式(1)で表される構造単位の含有量をa(モル%)、滴下に要した水酸化ナトリウム水溶液の量をV1(mL)、空試験に要した水酸化ナトリウム水溶液の量をV2(mL)とすると、以下の等式が成立するから、当該等式に滴定結果を代入し、式(1)で表される構造単位の含有量aを算出した。
で表されるコバルト錯体を用いることができる。
コーティング用組成物として用いる場合には、例えば、本開示の脂肪族ポリカーボネート10質量部に対して、モノマーを10〜70質量部程度含有するものが好ましい。当該モノマーの含有比率範囲は、下限が、11、12、13、14、15、16、17、18、19、20、21、22、23、24、又は25質量部程度であってもよく、また上限が69、68、67、66、65、64、63、62、61、60、59、58、57、56、55、54、53、52、51、又は50質量部程度であってもよい。また、特に硬化剤を組み合わせて用いる場合には、本開示の脂肪族ポリカーボネート10質量部に対して、10〜70質量部程度含有するものが好ましい。当該モノマーの含有比率範囲は、下限が、11、12、13、14、15、16、17、18、19、20、21、22、23、24、又は25質量部程度であってもよく、また上限が69、68、67、66、65、64、63、62、61、60、59、58、57、56、55、54、53、52、51、又は50質量部程度であってもよい。モノマーと硬化剤とを同量程度用いることがより好ましい。
試料(脂肪族ポリカーボネート)2.0gをテトラヒドロフラン/水=10/1(wt/wt)溶液40.0gに溶解させ、その溶液を0.1mol/L水酸化ナトリウム水溶液で中和滴定を行い、要した水酸化ナトリウム水溶液の量、空試験(脂肪族ポリカーボネートを含まない溶液を用いた測定)に要した水酸化ナトリウム水溶液の量から樹脂中の式(1)で表される構造単位の含有量を算出した。より詳細には、式(1)、式(2)の構造単位の分子量をそれぞれF1、F2、式(1)で表される構造単位の含有量をa(モル%)、滴下に要した水酸化ナトリウム水溶液の量をV1(mL)、空試験に要した水酸化ナトリウム水溶液の量をV2(mL)とすると、以下の等式が成立するから、当該等式に滴定結果を代入し、式(1)で表される構造単位の含有量aを算出した。
脂肪族ポリカーボネート濃度が0.2質量%のN,N−ジメチルホルムアミド溶液を調製し、高速液体クロマトグラフ(HPLC)を用いて測定した。測定後、同一条件で測定した質量平均分子量が既知のポリスチレンと比較することにより、質量平均分子量を算出した。
測定条件は、以下の通りである。
カラム:GPCカラム(昭和電工株式会社の商品名、Shodex OHPac SB−804,SB−805)
カラム温度:40℃
溶出液:5mmol/L LiBr−N,N−ジメチルホルムアミド溶液
流速:1.0mL/min
日立ハイテクサイエンス社製TG/DTA6200を用い、窒素雰囲気下、10℃/minの昇温速度で室温から500℃まで昇温して、熱分解挙動を測定し、熱重量曲線および示差熱曲線を得た。熱分解開始温度は、熱重量曲線における試験加熱開始前の質量を通る横軸に平行な線と、重量曲線における屈曲点間の勾配が最大となるように引いた接線との交点とした。分解反応における発熱ピークの有無は示差熱曲線におけるベースラインよりも上に凸となるピークの有無で判断した(上に凸となるピークが発熱ピークを表す)。400℃残査量は熱重量曲線上の温度400℃における重量から計算した。
冷却管、温度計及び攪拌機を備え付けた300mL容四つ口フラスコに、酸化亜鉛6.10g(0.075mol)、グルタル酸9.50g(0.15mol)、酢酸0.08g(0.003mol)及びトルエン160.00gを仕込んだ。次いで、窒素雰囲気下で60℃まで昇温し、さらに同温度で4時間攪拌して反応させた。その後、110℃まで昇温し、さらに同温度で4時間攪拌し、共沸蒸留により水分を除去した後、室温まで冷却して、亜鉛触媒を含む触媒スラリーを130.21g得た。
〔脂肪族ポリカーボネート前駆体1の製造〕
得られた脂肪族ポリカーボネート前駆体1の質量平均分子量は356,000であり、アリル基の含有量(すなわち、当該前駆体1における、式(1)の構造単位の前駆体単位の含有率)は0.70モル%であった。当該値は、1H−NMRの結果から算出した。具体的には、5.8ppm付近のアリル基由来のピークの積分値をA、5.0ppm付近のカーボネート基に隣接するメチン水素に由来するピークの積分値をBとし、次の等式を用いて算出した。
中和滴定により算出された、得られた脂肪族ポリカーボネート中、式(1)で表される構造単位の含有量は0.66モル%であった。
プロピレンオキシド及びアリルグリシジルエーテルの使用量を表1に示す量に変更した以外は実施例1と同様に反応を行うことにより、脂肪族ポリカーボネートを得た。
アリルグリシジルエーテルを使用しない以外は実施例1と同様の反応を行うことにより、脂肪族ポリカーボネート130gを得た。
プロピレンオキシド及びアリルグリシジルエーテルの使用量を表1に示す量に変更した以外は実施例1と同様に反応を行うことにより、脂肪族ポリカーボネートを得た。
〔脂肪族ポリカーボネート前駆体2の製造〕
得られた脂肪族ポリカーボネート前駆体2の質量平均分子量は286,000であり、ベンジル基の含有量(すなわち、当該前駆体における式(1)の構造単位の含有率)は1.48モル%であった。当該値は、1H−NMRの結果から算出した。具体的には、7.3ppm付近のフェニル基由来のピークの積分値をC、1.3ppm付近のメチル基に由来するピークの積分値をDとし、次の等式を用いて算出した。
1H−NMR(CDCl3)δ=5.05−4.95(1H),4.51−4.23(2H),2.80−2.73(2H),1.86−1.65(4H),1.31(3H)ppm.
中和滴定により算出された、得られた脂肪族ポリカーボネート中、式(1)で表される構造単位の含有量は1.48モル%であった。
攪拌機、ガス導入管、温度計を備えた1L容のセパラブルフラスコを窒素置換した後、実施例4で得られた脂肪族ポリカーボネート100.00g、酢酸エチル560.00g、ヘキサメチレンジイソシアネート5.0gを仕込み、攪拌しながら、50℃に昇温し、その温度で1時間攪拌した。その後、反応溶液を乾燥させることにより架橋剤(ヘキサメチレンジイソシアネート)を含む脂肪族ポリカーボネート含有組成物105.0gを得た。当該反応により、一部の架橋剤は脂肪族ポリカーボネートと反応し、架橋済み脂肪族ポリカーボネートが得られた。なお、当該組成物を上述したようにしてHPLCにより解析したところ、得られた架橋済み脂肪族ポリカーボネートの質量平均分子量は317400であった。
表2に記載の材料を酢酸エチルに均一に溶解させることで接着剤組成物を得た。例えば、評価例1−aは、脂肪族ポリカーボネート100部に架橋剤7部を組み合わせて用いたことを示す。なお、以下表中の「部」は質量部を示す。なお、実施例8の脂肪族ポリカーボネート樹脂組成物を使用した評価例では、すでに架橋剤が含まれているため、接着剤組成物を作成する際には新たな架橋剤は混合しなかった。得られた接着剤組成物をアルミニウム箔に塗布した後、40℃で6時間乾燥させ、試験片を作成した。試験片をSUS304板に130℃、1分間、5.0MPaの圧力で圧着し、24時間放置後、JIS K 6854−2:1999に従い、100mm/minの引張速度で180°剥離試験を行った。評価結果を表2にまとめた。
表3に記載の材料をフェノキシエタノールに加え、500rpmで1時間攪拌し、インク組成物を得た。得られたインク組成物を15cmの沈降管に充填し、40℃で7日間保存し、1日後又は7日後に、液面上部から2cm下の部分の濁度を目視で確認し沈降性を評価した。初期段階と変化が見られなかった場合はA、初期状態と並べて比較しないと変化が認識できない程度に若干薄くなった場合はB、明らかに薄くなった場合はC、完全に沈降し濁りが見られない場合はDとした。
表4に記載の材料をメチルエチルケトンに加え、均一に溶解させコーティング用組成物を得た。得られたコーティング用組成物を、アプリケータを用いて脱脂処理を施したガラス基板上に塗布した。その後、60℃で5時間を乾燥させ、さらに180℃で5時間加熱し、コーティング膜を備えたガラス基板を作成した。基材との密着性はJIS K 5600−5−6:1999に従い評価した。剥離が全く見られなかった場合をA、15%未満の剥離が見られた場合をB、15%以上の剥離が見られた場合をCとした。
チタン酸バリウム100部、脂肪族ポリカーボネート15部をメチルエチルケトンに加え、ボールミルを用いて分散した後、アプリケータを用いてのシート状に成形し、60℃で溶剤を乾燥させた。得られたシートの密度をシートの寸法と重量から求め、さらに用いたチタン酸バリウム、脂肪族ポリカーボネートの重量、比重からそれぞれの体積を算出し、シートの理論密度を求め、以下の計算からシートの空隙率を求めた。
空隙率(%)=(1−測定したシート密度/シートの理論密度)×100
シートの理論密度=(チタン酸バリウム重量+脂肪族ポリカーボネート重量)/(チタン酸バリウム体積+脂肪族ポリカーボネート体積)
空隙率が0以上10%未満をA、10%以上20%未満をB、20%以上をCと評価した。
また、評価に用いた脂肪族ポリカーボネートの熱分解測定を行い、熱分解開始温度、400℃残査量、分解反応における発熱ピークの有無を評価した。
チタン酸バリウム100部、脂肪族ポリカーボネート5部をメチルエチルケトンに加え、ボールミルを用いて分散を行い、島津製作所製レーザー回折式粒度分布計SALD−7100を用いて、分散前後の粒度分布の変化を測定した。原料であるチタン酸バリウムよりも粒度分布が狭くなった場合はA、粒度分布がほとんど変化しなかった場合はB、粒度分布が広くなり明らかな凝集が見られた場合はCと評価した。
Claims (11)
- 式(1):
式(1)で表される構造単位の含有量が、式(1)と式(2)の構造単位の合計量に対して、0.1モル%以上1.5モル%以下である、脂肪族ポリカーボネート。 - 質量平均分子量が6万以上100万以下である請求項1に記載の脂肪族ポリカーボネート。
- 式(1)のXにおいて、ヘテロ原子を含む2価の基が、酸素原子、窒素原子、及び硫黄原子からなる群より選択される少なくとも1種の原子を含む基である、請求項1又は2に記載の脂肪族ポリカーボネート。
- 式(1)で表される構造単位及び式(2)で表される構造単位のみからなる、請求項1〜4のいずれかに記載の脂肪族ポリカーボネート。
- 請求項1〜5のいずれかに記載の脂肪族ポリカーボネートと架橋剤とを含む脂肪族ポリカーボネート組成物。
- 請求項1〜5のいずれかに記載の脂肪族ポリカーボネート、又は請求項6に記載の脂肪族ポリカーボネート組成物を用いて得られる接着剤組成物。
- 請求項1〜5のいずれかに記載の脂肪族ポリカーボネート、又は請求項6に記載の脂肪族ポリカーボネート組成物を含むインク組成物。
- 請求項1〜5のいずれかに記載の脂肪族ポリカーボネート、又は請求項6に記載の脂肪族ポリカーボネート組成物を含むコーティング用組成物。
- 請求項1〜5のいずれかに記載の脂肪族ポリカーボネート、又は請求項6に記載の脂肪族ポリカーボネート組成物を含む焼成用バインダー。
- 請求項1〜5のいずれかに記載の脂肪族ポリカーボネート、又は請求項6に記載の脂肪族ポリカーボネート組成物を含む分散剤。
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