JP6877707B2 - ベンゾトリアゾール系重合体を含有する樹脂組成物 - Google Patents
ベンゾトリアゾール系重合体を含有する樹脂組成物 Download PDFInfo
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- JP6877707B2 JP6877707B2 JP2017155735A JP2017155735A JP6877707B2 JP 6877707 B2 JP6877707 B2 JP 6877707B2 JP 2017155735 A JP2017155735 A JP 2017155735A JP 2017155735 A JP2017155735 A JP 2017155735A JP 6877707 B2 JP6877707 B2 JP 6877707B2
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- benzotriazole
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- resin
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- 239000011342 resin composition Substances 0.000 title claims description 36
- 229920000642 polymer Polymers 0.000 title description 42
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 title description 13
- 239000012964 benzotriazole Substances 0.000 title description 13
- -1 benzotriazole derivative compound Chemical class 0.000 claims description 59
- 229920005989 resin Polymers 0.000 claims description 46
- 239000011347 resin Substances 0.000 claims description 46
- 239000000463 material Substances 0.000 claims description 18
- 229920001519 homopolymer Polymers 0.000 claims description 17
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 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
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 3
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 3
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 3
- 125000003944 tolyl group Chemical group 0.000 claims description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 78
- 150000001875 compounds Chemical class 0.000 description 49
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 39
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 27
- 238000005259 measurement Methods 0.000 description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 26
- 239000000203 mixture Substances 0.000 description 25
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 24
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 19
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 18
- 238000000034 method Methods 0.000 description 18
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 18
- 230000015572 biosynthetic process Effects 0.000 description 16
- 238000003786 synthesis reaction Methods 0.000 description 16
- 239000000243 solution Substances 0.000 description 15
- 239000013078 crystal Substances 0.000 description 14
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 13
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 13
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 12
- 229920001577 copolymer Polymers 0.000 description 12
- 238000006116 polymerization reaction Methods 0.000 description 11
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 10
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 10
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 10
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 9
- 229910000029 sodium carbonate Inorganic materials 0.000 description 9
- 239000006096 absorbing agent Substances 0.000 description 8
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- 238000004128 high performance liquid chromatography Methods 0.000 description 8
- 238000010992 reflux Methods 0.000 description 8
- 239000002904 solvent Substances 0.000 description 8
- AHQCTPQBXNKFJH-UHFFFAOYSA-N 4-(5-methoxybenzotriazol-2-yl)benzene-1,3-diol Chemical compound N1=C2C=C(OC)C=CC2=NN1C1=CC=C(O)C=C1O AHQCTPQBXNKFJH-UHFFFAOYSA-N 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 6
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 6
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 239000003505 polymerization initiator Substances 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 239000004342 Benzoyl peroxide Substances 0.000 description 5
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 5
- 238000005481 NMR spectroscopy Methods 0.000 description 5
- 238000010521 absorption reaction Methods 0.000 description 5
- 235000019400 benzoyl peroxide Nutrition 0.000 description 5
- 239000002270 dispersing agent Substances 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- VVBLNCFGVYUYGU-UHFFFAOYSA-N 4,4'-Bis(dimethylamino)benzophenone Chemical compound C1=CC(N(C)C)=CC=C1C(=O)C1=CC=C(N(C)C)C=C1 VVBLNCFGVYUYGU-UHFFFAOYSA-N 0.000 description 4
- 238000002835 absorbance Methods 0.000 description 4
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical class C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 4
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 4
- 239000003999 initiator Substances 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 4
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- 229920002554 vinyl polymer Polymers 0.000 description 4
- 238000005160 1H NMR spectroscopy Methods 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- VJTAQCFWGQRRSZ-UHFFFAOYSA-N 2-[5-(2-hydroxyethoxy)benzotriazol-2-yl]-5-octoxyphenol Chemical compound OCCOC1=CC=2C(=NN(N2)C2=C(C=C(C=C2)OCCCCCCCC)O)C=C1 VJTAQCFWGQRRSZ-UHFFFAOYSA-N 0.000 description 3
- SZIFAVKTNFCBPC-UHFFFAOYSA-N 2-chloroethanol Chemical compound OCCCl SZIFAVKTNFCBPC-UHFFFAOYSA-N 0.000 description 3
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- 238000000862 absorption spectrum Methods 0.000 description 3
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 3
- 239000012965 benzophenone Substances 0.000 description 3
- 150000001565 benzotriazoles Chemical class 0.000 description 3
- LWMFAFLIWMPZSX-UHFFFAOYSA-N bis[2-(4,5-dihydro-1h-imidazol-2-yl)propan-2-yl]diazene Chemical compound N=1CCNC=1C(C)(C)N=NC(C)(C)C1=NCCN1 LWMFAFLIWMPZSX-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 230000018044 dehydration Effects 0.000 description 3
- 238000006297 dehydration reaction Methods 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- 229940098779 methanesulfonic acid Drugs 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 239000004417 polycarbonate Substances 0.000 description 3
- 229920000515 polycarbonate Polymers 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 239000007870 radical polymerization initiator Substances 0.000 description 3
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 3
- 0 *Oc1cc(O)c(*2NC(C=C(C=C3)O)C3=*2)cc1 Chemical compound *Oc1cc(O)c(*2NC(C=C(C=C3)O)C3=*2)cc1 0.000 description 2
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- UHFFVFAKEGKNAQ-UHFFFAOYSA-N 2-benzyl-2-(dimethylamino)-1-(4-morpholin-4-ylphenyl)butan-1-one Chemical compound C=1C=C(N2CCOCC2)C=CC=1C(=O)C(CC)(N(C)C)CC1=CC=CC=C1 UHFFVFAKEGKNAQ-UHFFFAOYSA-N 0.000 description 2
- KTALPKYXQZGAEG-UHFFFAOYSA-N 2-propan-2-ylthioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(C(C)C)=CC=C3SC2=C1 KTALPKYXQZGAEG-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- IVTPGIYEKCIBMD-UHFFFAOYSA-N C(C)OC=1C=CC(=C(C1)O)N1N=C2C(=N1)C=CC(=C2)OCCO Chemical compound C(C)OC=1C=CC(=C(C1)O)N1N=C2C(=N1)C=CC(=C2)OCCO IVTPGIYEKCIBMD-UHFFFAOYSA-N 0.000 description 2
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical class [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- NPKSPKHJBVJUKB-UHFFFAOYSA-N N-phenylglycine Chemical compound OC(=O)CNC1=CC=CC=C1 NPKSPKHJBVJUKB-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
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- 244000028419 Styrax benzoin Species 0.000 description 2
- 235000000126 Styrax benzoin Nutrition 0.000 description 2
- 235000008411 Sumatra benzointree Nutrition 0.000 description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- 229960002130 benzoin Drugs 0.000 description 2
- 230000000740 bleeding effect Effects 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 235000019382 gum benzoic Nutrition 0.000 description 2
- 229920000609 methyl cellulose Polymers 0.000 description 2
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- 235000010981 methylcellulose Nutrition 0.000 description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
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- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
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- 229920006027 ternary co-polymer Polymers 0.000 description 2
- FVQMJJQUGGVLEP-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOOC(C)(C)C FVQMJJQUGGVLEP-UHFFFAOYSA-N 0.000 description 1
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
- 229920003067 (meth)acrylic acid ester copolymer Polymers 0.000 description 1
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- MPPPKRYCTPRNTB-UHFFFAOYSA-N 1-bromobutane Chemical compound CCCCBr MPPPKRYCTPRNTB-UHFFFAOYSA-N 0.000 description 1
- CNDHHGUSRIZDSL-UHFFFAOYSA-N 1-chlorooctane Chemical compound CCCCCCCCCl CNDHHGUSRIZDSL-UHFFFAOYSA-N 0.000 description 1
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 description 1
- KWVGIHKZDCUPEU-UHFFFAOYSA-N 2,2-dimethoxy-2-phenylacetophenone Chemical compound C=1C=CC=CC=1C(OC)(OC)C(=O)C1=CC=CC=C1 KWVGIHKZDCUPEU-UHFFFAOYSA-N 0.000 description 1
- RPZANUYHRMRTTE-UHFFFAOYSA-N 2,3,4-trimethoxy-6-(methoxymethyl)-5-[3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxyoxane;1-[[3,4,5-tris(2-hydroxybutoxy)-6-[4,5,6-tris(2-hydroxybutoxy)-2-(2-hydroxybutoxymethyl)oxan-3-yl]oxyoxan-2-yl]methoxy]butan-2-ol Chemical compound COC1C(OC)C(OC)C(COC)OC1OC1C(OC)C(OC)C(OC)OC1COC.CCC(O)COC1C(OCC(O)CC)C(OCC(O)CC)C(COCC(O)CC)OC1OC1C(OCC(O)CC)C(OCC(O)CC)C(OCC(O)CC)OC1COCC(O)CC RPZANUYHRMRTTE-UHFFFAOYSA-N 0.000 description 1
- MDKSQNHUHMMKPP-UHFFFAOYSA-N 2,5-bis(4-methoxyphenyl)-4-phenyl-1h-imidazole Chemical class C1=CC(OC)=CC=C1C1=NC(C=2C=CC=CC=2)=C(C=2C=CC(OC)=CC=2)N1 MDKSQNHUHMMKPP-UHFFFAOYSA-N 0.000 description 1
- LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 description 1
- CTWRMVAKUSJNBK-UHFFFAOYSA-N 2-(2,4-dimethoxyphenyl)-4,5-diphenyl-1h-imidazole Chemical class COC1=CC(OC)=CC=C1C1=NC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)N1 CTWRMVAKUSJNBK-UHFFFAOYSA-N 0.000 description 1
- RXAYEPUDXSKVHS-UHFFFAOYSA-N 2-(2-chlorophenyl)-4,5-bis(3-methoxyphenyl)-1h-imidazole Chemical class COC1=CC=CC(C2=C(NC(=N2)C=2C(=CC=CC=2)Cl)C=2C=C(OC)C=CC=2)=C1 RXAYEPUDXSKVHS-UHFFFAOYSA-N 0.000 description 1
- NSWNXQGJAPQOID-UHFFFAOYSA-N 2-(2-chlorophenyl)-4,5-diphenyl-1h-imidazole Chemical class ClC1=CC=CC=C1C1=NC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)N1 NSWNXQGJAPQOID-UHFFFAOYSA-N 0.000 description 1
- AVTLBBWTUPQRAY-UHFFFAOYSA-N 2-(2-cyanobutan-2-yldiazenyl)-2-methylbutanenitrile Chemical compound CCC(C)(C#N)N=NC(C)(CC)C#N AVTLBBWTUPQRAY-UHFFFAOYSA-N 0.000 description 1
- UIHRWPYOTGCOJP-UHFFFAOYSA-N 2-(2-fluorophenyl)-4,5-diphenyl-1h-imidazole Chemical class FC1=CC=CC=C1C1=NC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)N1 UIHRWPYOTGCOJP-UHFFFAOYSA-N 0.000 description 1
- WCQGGJUMXRCNBX-UHFFFAOYSA-N 2-(2-hydroxy-4-octoxyphenyl)benzotriazol-5-ol Chemical compound CCCCCCCCOc1ccc(c(O)c1)-n1nc2ccc(O)cc2n1 WCQGGJUMXRCNBX-UHFFFAOYSA-N 0.000 description 1
- XIOGJAPOAUEYJO-UHFFFAOYSA-N 2-(2-methoxyphenyl)-4,5-diphenyl-1h-imidazole Chemical class COC1=CC=CC=C1C1=NC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)N1 XIOGJAPOAUEYJO-UHFFFAOYSA-N 0.000 description 1
- FLJBBHRQCKCGAO-UHFFFAOYSA-N 2-(2-propan-2-yl-4,5-dihydroimidazol-1-yl)ethanol;dihydrochloride Chemical compound Cl.Cl.CC(C)C1=NCCN1CCO FLJBBHRQCKCGAO-UHFFFAOYSA-N 0.000 description 1
- RLAJUWSTNRXTQG-UHFFFAOYSA-N 2-(5-methoxybenzotriazol-2-yl)-5-octoxyphenol Chemical compound OC1=CC(OCCCCCCCC)=CC=C1N1N=C2C=C(OC)C=CC2=N1 RLAJUWSTNRXTQG-UHFFFAOYSA-N 0.000 description 1
- GJKGAPPUXSSCFI-UHFFFAOYSA-N 2-Hydroxy-4'-(2-hydroxyethoxy)-2-methylpropiophenone Chemical compound CC(C)(O)C(=O)C1=CC=C(OCCO)C=C1 GJKGAPPUXSSCFI-UHFFFAOYSA-N 0.000 description 1
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
- NLGDWWCZQDIASO-UHFFFAOYSA-N 2-hydroxy-1-(7-oxabicyclo[4.1.0]hepta-1,3,5-trien-2-yl)-2-phenylethanone Chemical class OC(C(=O)c1cccc2Oc12)c1ccccc1 NLGDWWCZQDIASO-UHFFFAOYSA-N 0.000 description 1
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- 229940079827 sodium hydrogen sulfite Drugs 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000010558 suspension polymerization method Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- OZTYRAWXWCSOAF-DIYDOPDJSA-N tetramethylsilane;trichloro(deuterio)methane Chemical compound [2H]C(Cl)(Cl)Cl.C[Si](C)(C)C OZTYRAWXWCSOAF-DIYDOPDJSA-N 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Landscapes
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
[式中、R1は水素原子、炭素数1〜8のアルキル基、フェニル基、トリル基、ホルミル基、アルキル炭素数1〜7のアルキルカルボニル基、ベンゾイル基、またはトルオイル基を表し、R2は炭素数1〜8のアルキレン基を表し、R3は水素原子、またはメチル基を表す]
<測定条件>
装置:L−2130((株)日立ハイテクノロジーズ製)
使用カラム:SUMIPAX ODS A−212 6×150mm 5μm
カラム温度:40℃
移動相: メタノール/水=99/1
流速:1.0ml/min
<測定結果>
HPLC面百純度:99.9%
なお、以下の化合物(b)も化合物(a)と同様の測定条件でHPLC分析を行った。
<測定条件>
装置:UV−2450((株)島津製作所製)
測定波長:250〜 450nm
溶媒:クロロホルム
濃度:10ppm
セル:1cm石英
なお、以下の化合物(b)、(c)、(d)も化合物(a)と同様の測定条件で紫外〜可視吸収スペクトルの測定を行った。
<測定条件>
装置:JEOL AL−300
共鳴周波数:300MHz(1H−NMR)
溶媒:クロロホルム−d
1H−NMRの内部標準物質として、テトラメチルシランを用い、ケミカルシフト値はδ値(ppm)、カップリング定数はHertzで示した。またsはsinglet、dはdoublet、tはtriplet、ddはdouble doublet、mはmultiplet、bはbroadの略とする。以下の化合物(b)、(c)、(d)においても同様である。得られたNMRスペクトルの内容は以下のとおりである。
δ=11.3(s,OH),8.19(d,1H,J=9.9Hz,benzotriazole−H),7.78(dd,1H,J=9.92Hz,J=0.96Hz,J=0.87Hz,benzotriazole−H),7.0−7.3(m,2H,benzotriazole−H,phenol−H),6.67(d,1H,J=2.91Hz,phenol−H),6.59(dd,1H,J=10.2Hz,J=2.94Hz,J=3.06Hz,=CH2−H),6.17(s,1H,phenol−H),5.61(t,1H,=CH2−H),4.57(t,2H,O−CH2−CH2−O−H),4.32(t,2H,O−CH2−CH2−O−H),4.00(t,2H,pH−O−CH2−H),1.80(m,2H,CH2−H),1.2−1.6(m,10H,(CH2)5−H),0.89(s,3H,CH3−H)
<測定条件>
装置: VARIAN Mercury300
共振周波数:300MHz(1H−NMR)
溶媒:クロロホルム−d
得られたNMRスペクトルの内容は以下のとおりである。なお、以下の化合物(c)、(d)も化合物(b)と同様の測定条件でNMR測定を行った。
δ=11.3(b,OH),8.21(d,1H,J=9.07Hz,benzotriazole−H),7.79(d,1H,J=9.07Hz,benzotriazole−H),7.18(d,1H,J=2.3Hz,phenol−H),7.16(d,1H,J=2.3Hz,phenol−H),7.15(d,1H,J=1.81,benzotriazole−H,),6.67(s,1H,phenol−H),6.60(m,1H,=CH2−H),6.20(q,1H,CH=−H),5.89(dd,1H,J=10.5Hz,J=0.66Hz,J=0.75Hz,=CH2−H),4.32(t,2H,O−CH2−CH2−O−H),4.00(t,2H,O−CH2−CH2−O−H),0.8−2(m,17H,n−C8H17−H)
<測定条件>
装置:L−2130((株)日立ハイテクノロジーズ製)
使用カラム:Inertsil ODS−3 4.6×150mm 5μm
カラム温度:25℃
移動相: アセトニトリル/水=9/1(リン酸3ml/L)
流速:1.0ml/min
<測定結果>
HPLC面百純度:98.7%
なお、以下の化合物(d)も化合物(c)と同様の測定条件でHPLC測定を行った。
δ=11.3(b,OH),8.21(d,1H,J=9.24Hz,benzotriazole−H),7.80(dd,1H,J=9.1Hz,J=0.66Hz,J=0.66Hz,benzotriazole−H),7.18(d,1H,J=2.31Hz,phenol−H),6.68(d,1H,J=2.64Hz,phenol−H),6.60(dd,1H,J=9.2Hz,J=2.64Hz,J=2.64Hz,benzotriazole−H,),6.18(s,1H,=CH2−H),5.62(m,1H,=CH2−H),0.9−2.1(m,3H,9H,CH3,n−C4H9−H)
δ=11.3(b,OH),8.21(d,1H,J=9.07Hz,benzotriazole−H),7.79(d,1H,J=9.72,benzotriazole−H),7.16(m,1H,phenol−H),6.68(d,1H,J=2.64Hz,phenol−H),6.59(dd,1H,J=9.2,J=2.8,J=2.64,phenol−H,),6.17(s,1H,C=CH2−H),5.61(t,1H,=CH2−H),4.58(m,2H,O−CH2−CH2−O−H),4.32(t,2H,O−CH2−CH2−O−H),4.08(q,2H,−CH2−CH3−H),1.67(s,3H,C=CH2−CH3−H),1.57(t,3H,CH2−CH3−H)
[重合体(a);化合物(a)の濃度0.025Mの単独重合]
100mlのガラス管に、化合物(a);2−[2−(2−ヒドロキシ−4−オクチルオキシフェニル)−2H−ベンゾトリアゾール−5−イルオキシ]エチルメタクリレートを0.234g(0.0005モル)、ベンゼン20ml、ベンゾイルパーオキサイド0.097g(0.0004モル)を入れて、凍結乾燥した後に封管した。ガラス管を90℃のオイルバスに入れて24時間重合させた。重合溶液を100mlフラスコへ移し、エバポレーターでベンゼンを留去した。そこへクロロホルム10mlを加えて生成物を溶解させ、その溶液を200mlのアセトンの中へ滴下した。析出したポリマーをろ過し、アセトン100mlで洗浄した後、減圧下室温で乾燥し、淡黄色固体の重合体(a)を0.147g得た。
<測定条件>
装置:LC−10AD((株)島津製作所製)
溶離液:クロロホルム
カラム:Shodex K−807L、Shodex K805L、Shodex K−804L(昭和電工(株)製)
吸収スペクトル削除
[重合体(b);化合物(a)の濃度0.050Mの単独重合]
100mlのガラス管に、化合物(a);2−[2−(2−ヒドロキシ−4−オクチルオキシフェニル)−2H−ベンゾトリアゾール−5−イルオキシ]エチルメタクリレートを0.468g(0.001モル)、ベンゼン20ml、ベンゾイルパーオキサイド0.097g(0.0004モル)を入れて、凍結乾燥した後に封管した。ガラス管を90℃のオイルバスに入れて24時間重合させた。重合溶液を100mlフラスコへ移し、エバポレーターでベンゼンを留去した。そこへクロロホルム10mlを加えて生成物を溶解させ、その溶液を200mlのアセトンの中へ滴下した。析出したポリマーをろ過し、アセトン100mlで洗浄した後、減圧下室温で乾燥し、淡黄色固体の重合体(b)を0.337g得た。
[重合体(c);化合物(a)の濃度0.075Mの単独重合]
100mlのガラス管に、化合物(a);2−[2−(2−ヒドロキシ−4−オクチルオキシフェニル)−2H−ベンゾトリアゾール−5−イルオキシ]エチルメタクリレートを0.702g(0.0015モル)、ベンゼン20ml、ベンゾイルパーオキサイド0.097g(0.0004モル)を入れて、凍結乾燥した後に封管した。ガラス管を90℃のオイルバスに入れて24時間重合させた。重合溶液を100mlフラスコへ移し、エバポレーターでベンゼンを留去した。そこへクロロホルム15mlを加えて生成物を溶解させ、その溶液を300mlのアセトンの中へ滴下した。析出したポリマーをろ過し、アセトン100mlで洗浄した後、減圧下室温で乾燥し、淡黄色固体の重合体(c)を0.597g得た。
[重合体(d);化合物(a)の濃度0.1Mの単独重合]
100mlのガラス管に、化合物(a);2−[2−(2−ヒドロキシ−4−オクチルオキシフェニル)−2H−ベンゾトリアゾール−5−イルオキシ]エチルメタクリレートを0.936g(0.002モル)、ベンゼン20ml、ベンゾイルパーオキサイド0.097g(0.0004モル)を入れて、凍結乾燥した後に封管した。ガラス管を90℃のオイルバスに入れて24時間重合させた。重合溶液を100mlフラスコへ移し、エバポレーターでベンゼンを留去した。そこへクロロホルム20mlを加えて生成物を溶解させ、その溶液を400mlのアセトンの中へ滴下した。析出したポリマーをろ過し、アセトン100mlで洗浄した後、減圧下室温で乾燥し、淡黄色固体の重合体(d)を0.861g得た。
また、重合体(d)の分子量を測定した結果、重量平均分子量(Mw)は54900、数平均分子量(Mn)は17100、多分散度(Mw/Mn)は3.21であった。
[樹脂組成物の作製]
合成例1で得られた重合体(a)と、ポリスチレン、ポリカーボネート、またはポリメタクリル酸メチルと、ジクロロメタンを表1で示す比率で混合し、紫外線吸収剤を含有した樹脂組成物の溶液を得た。得られた紫外線吸収剤を含有した樹脂組成物の溶液20mlを、直径12cmのシャーレに移し、25℃での常圧乾燥を48時間実施して溶媒を除去し、膜厚20μmの紫外線吸収剤を1%または20%含んだ樹脂組成物を得た。また、比較として、重合体(c)及び重合体(d)と、従来の一般的な紫外線吸収剤である化合物(e);2−(2H−ベンゾトリアゾール−2−イル]−4−メチルフェノールを含有する樹脂組成物も同様に作製した。
上記で得られた紫外線吸収剤を20%含んだ樹脂組成物の耐熱性を、示差熱熱重量同時測定装置を用いて測定した結果を、表2に示す。
上記で得られた紫外線吸収剤を1%含んだ樹脂組成物表面の光沢度を表3に示す。樹脂素材と紫外線吸収剤の相溶性が不十分な場合、紫外線吸収剤が樹脂組成物表面にブリードアウトしてくることから、樹脂組成物表面にざらつきが出て、光沢度が低下する。よって光沢度は、樹脂素材と紫外線吸収剤の相溶性の指標となる。
装置:TG/DTA6300(セイコーインスツル(株)製)
測定温度:100〜500℃
昇温速度:10℃/分
測定雰囲気:窒素
装置:UNI GLOSS60(コニカミノルタセンシング(株)製)
測定角度:60°
Claims (3)
- 前記単独重合体を構成する前記ベンゾトリアゾール誘導体化合物において、前記一般式(1)のR1が炭素数2〜8のアルキル基であり、R2がエチレン基である請求項1記載の樹脂組成物。
- 前記単独重合体が、前記樹脂素材に対して0.01〜20重量%の範囲で含まれている請求項1または2記載の樹脂組成物。
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