JP2014031510A - 安定化剤組成物 - Google Patents
安定化剤組成物 Download PDFInfo
- Publication number
- JP2014031510A JP2014031510A JP2013146007A JP2013146007A JP2014031510A JP 2014031510 A JP2014031510 A JP 2014031510A JP 2013146007 A JP2013146007 A JP 2013146007A JP 2013146007 A JP2013146007 A JP 2013146007A JP 2014031510 A JP2014031510 A JP 2014031510A
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- JP
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- Prior art keywords
- group
- acrylate
- meth
- tert
- methyl
- Prior art date
- 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.)
- Granted
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- 239000000203 mixture Substances 0.000 title claims abstract description 169
- 239000003381 stabilizer Substances 0.000 title claims abstract description 81
- -1 ester compounds Chemical class 0.000 claims abstract description 163
- 229920000642 polymer Polymers 0.000 claims abstract description 56
- 150000001875 compounds Chemical class 0.000 claims abstract description 28
- 150000003568 thioethers Chemical class 0.000 claims abstract description 25
- 239000000539 dimer Substances 0.000 claims abstract description 20
- 150000002989 phenols Chemical class 0.000 claims abstract description 19
- 230000000087 stabilizing effect Effects 0.000 claims abstract description 4
- ZPEIXKMOUCYBEB-UHFFFAOYSA-N 4-hydroxy-1,3,2,4-dioxathiaphosphetane Chemical compound S1OP(O1)O ZPEIXKMOUCYBEB-UHFFFAOYSA-N 0.000 claims description 21
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims description 18
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims description 9
- 230000000379 polymerizing effect Effects 0.000 claims description 5
- 238000004040 coloring Methods 0.000 abstract description 30
- 230000037048 polymerization activity Effects 0.000 abstract description 24
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 abstract description 8
- 238000012423 maintenance Methods 0.000 abstract description 5
- 150000003003 phosphines Chemical class 0.000 abstract description 3
- 125000000446 sulfanediyl group Chemical group *S* 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 124
- 150000002148 esters Chemical class 0.000 description 73
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 52
- 150000003254 radicals Chemical class 0.000 description 48
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 35
- 241000953555 Theama Species 0.000 description 33
- 125000004432 carbon atom Chemical group C* 0.000 description 33
- 238000010526 radical polymerization reaction Methods 0.000 description 24
- 239000000126 substance Substances 0.000 description 24
- 238000012360 testing method Methods 0.000 description 21
- 125000000217 alkyl group Chemical group 0.000 description 20
- 238000006243 chemical reaction Methods 0.000 description 19
- 238000002156 mixing Methods 0.000 description 18
- 239000000178 monomer Substances 0.000 description 18
- 239000012321 sodium triacetoxyborohydride Substances 0.000 description 18
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 17
- 238000006116 polymerization reaction Methods 0.000 description 17
- 239000000243 solution Substances 0.000 description 17
- 229920005989 resin Polymers 0.000 description 16
- 239000011347 resin Substances 0.000 description 16
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 15
- 230000000052 comparative effect Effects 0.000 description 15
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 15
- 239000007870 radical polymerization initiator Substances 0.000 description 15
- 239000003513 alkali Substances 0.000 description 14
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 13
- 239000000047 product Substances 0.000 description 13
- 239000007788 liquid Substances 0.000 description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 12
- 238000003860 storage Methods 0.000 description 12
- 150000002430 hydrocarbons Chemical group 0.000 description 11
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 11
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical class CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 10
- 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 10
- 239000000463 material Substances 0.000 description 10
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 9
- 239000005977 Ethylene Substances 0.000 description 9
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- 239000011230 binding agent Substances 0.000 description 9
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical group OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 9
- 238000002360 preparation method Methods 0.000 description 9
- 239000002904 solvent Substances 0.000 description 9
- AYEKOFBPNLCAJY-UHFFFAOYSA-O thiamine pyrophosphate Chemical compound CC1=C(CCOP(O)(=O)OP(O)(O)=O)SC=[N+]1CC1=CN=C(C)N=C1N AYEKOFBPNLCAJY-UHFFFAOYSA-O 0.000 description 9
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 9
- WMYINDVYGQKYMI-UHFFFAOYSA-N 2-[2,2-bis(hydroxymethyl)butoxymethyl]-2-ethylpropane-1,3-diol Chemical compound CCC(CO)(CO)COCC(CC)(CO)CO WMYINDVYGQKYMI-UHFFFAOYSA-N 0.000 description 8
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical group C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 239000007787 solid Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 7
- 239000000853 adhesive Substances 0.000 description 7
- 230000001070 adhesive effect Effects 0.000 description 7
- 230000000704 physical effect Effects 0.000 description 7
- 239000002994 raw material Substances 0.000 description 7
- 150000005208 1,4-dihydroxybenzenes Chemical class 0.000 description 6
- ATVJXMYDOSMEPO-UHFFFAOYSA-N 3-prop-2-enoxyprop-1-ene Chemical compound C=CCOCC=C ATVJXMYDOSMEPO-UHFFFAOYSA-N 0.000 description 6
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 6
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical class CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000000654 additive Substances 0.000 description 6
- 125000001424 substituent group Chemical group 0.000 description 6
- HMUNWXXNJPVALC-UHFFFAOYSA-N 1-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C(CN1CC2=C(CC1)NN=N2)=O HMUNWXXNJPVALC-UHFFFAOYSA-N 0.000 description 5
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 5
- YJLUBHOZZTYQIP-UHFFFAOYSA-N 2-[5-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-1,3,4-oxadiazol-2-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1=NN=C(O1)CC(=O)N1CC2=C(CC1)NN=N2 YJLUBHOZZTYQIP-UHFFFAOYSA-N 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 5
- 125000002723 alicyclic group Chemical group 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 239000000839 emulsion Substances 0.000 description 5
- QYZFTMMPKCOTAN-UHFFFAOYSA-N n-[2-(2-hydroxyethylamino)ethyl]-2-[[1-[2-(2-hydroxyethylamino)ethylamino]-2-methyl-1-oxopropan-2-yl]diazenyl]-2-methylpropanamide Chemical compound OCCNCCNC(=O)C(C)(C)N=NC(C)(C)C(=O)NCCNCCO QYZFTMMPKCOTAN-UHFFFAOYSA-N 0.000 description 5
- 239000003973 paint Substances 0.000 description 5
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 5
- 239000003505 polymerization initiator Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- BGNXCDMCOKJUMV-UHFFFAOYSA-N Tert-Butylhydroquinone Chemical compound CC(C)(C)C1=CC(O)=CC=C1O BGNXCDMCOKJUMV-UHFFFAOYSA-N 0.000 description 4
- 239000007983 Tris buffer Substances 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 description 4
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 4
- 125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 4
- 229910001873 dinitrogen Inorganic materials 0.000 description 4
- 125000001033 ether group Chemical group 0.000 description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 4
- 239000000976 ink Substances 0.000 description 4
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 4
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- 238000013112 stability test Methods 0.000 description 4
- 125000000547 substituted alkyl group Chemical group 0.000 description 4
- 239000004250 tert-Butylhydroquinone Substances 0.000 description 4
- 235000019281 tert-butylhydroquinone Nutrition 0.000 description 4
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 4
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 4
- 229960000834 vinyl ether Drugs 0.000 description 4
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 3
- GXURZKWLMYOCDX-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol;dihydroxyphosphanyl dihydrogen phosphite Chemical compound OP(O)OP(O)O.OCC(CO)(CO)CO GXURZKWLMYOCDX-UHFFFAOYSA-N 0.000 description 3
- OPLCSTZDXXUYDU-UHFFFAOYSA-N 2,4-dimethyl-6-tert-butylphenol Chemical compound CC1=CC(C)=C(O)C(C(C)(C)C)=C1 OPLCSTZDXXUYDU-UHFFFAOYSA-N 0.000 description 3
- WZFUQSJFWNHZHM-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)N1CC2=C(CC1)NN=N2 WZFUQSJFWNHZHM-UHFFFAOYSA-N 0.000 description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 3
- VKLOPQHLJNFYKK-UHFFFAOYSA-N 3-dodecylsulfanylpropanoic acid Chemical compound CCCCCCCCCCCCSCCC(O)=O VKLOPQHLJNFYKK-UHFFFAOYSA-N 0.000 description 3
- BZGLBTNQDMGACY-UHFFFAOYSA-N 4,6-bis(dodecylsulfanylmethyl)-6-methylcyclohexa-1,3-dien-1-ol Chemical compound CCCCCCCCCCCCSCC1=CC=C(O)C(C)(CSCCCCCCCCCCCC)C1 BZGLBTNQDMGACY-UHFFFAOYSA-N 0.000 description 3
- UYQYTUYNNYZATF-UHFFFAOYSA-N 6-methyl-4,6-bis(octylsulfanylmethyl)cyclohexa-1,3-dien-1-ol Chemical compound CCCCCCCCSCC1=CC=C(O)C(C)(CSCCCCCCCC)C1 UYQYTUYNNYZATF-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical class C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- IISBACLAFKSPIT-UHFFFAOYSA-N Bisphenol A Natural products C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 3
- PXKLMJQFEQBVLD-UHFFFAOYSA-N Bisphenol F Natural products C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 3
- 229920002799 BoPET Polymers 0.000 description 3
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-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
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical group C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 description 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 3
- 125000004414 alkyl thio group Chemical group 0.000 description 3
- 239000007869 azo polymerization initiator Substances 0.000 description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
- 125000004851 cyclopentylmethyl group Chemical group C1(CCCC1)C* 0.000 description 3
- 239000005548 dental material Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 125000005982 diphenylmethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 238000007720 emulsion polymerization reaction Methods 0.000 description 3
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 3
- 125000005843 halogen group Chemical group 0.000 description 3
- 239000003999 initiator Substances 0.000 description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 239000012778 molding material Substances 0.000 description 3
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- 125000000962 organic group Chemical group 0.000 description 3
- 150000002978 peroxides Chemical class 0.000 description 3
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 3
- 239000003504 photosensitizing agent Substances 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 239000001294 propane Substances 0.000 description 3
- 229940095050 propylene Drugs 0.000 description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- 229930195734 saturated hydrocarbon Natural products 0.000 description 3
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 125000003944 tolyl group Chemical group 0.000 description 3
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 3
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- 125000006033 1,1-dimethyl-2-propenyl group Chemical group 0.000 description 2
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
- TYMYJUHDFROXOO-UHFFFAOYSA-N 1,3-bis(prop-2-enoxy)-2,2-bis(prop-2-enoxymethyl)propane Chemical compound C=CCOCC(COCC=C)(COCC=C)COCC=C TYMYJUHDFROXOO-UHFFFAOYSA-N 0.000 description 2
- UZKWTJUDCOPSNM-UHFFFAOYSA-N 1-ethenoxybutane Chemical compound CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 2
- VTFXHGBOGGGYDO-UHFFFAOYSA-N 2,4-bis(dodecylsulfanylmethyl)-6-methylphenol Chemical compound CCCCCCCCCCCCSCC1=CC(C)=C(O)C(CSCCCCCCCCCCCC)=C1 VTFXHGBOGGGYDO-UHFFFAOYSA-N 0.000 description 2
- 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 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
- SXAMGRAIZSSWIH-UHFFFAOYSA-N 2-[3-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-1,2,4-oxadiazol-5-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1=NOC(=N1)CC(=O)N1CC2=C(CC1)NN=N2 SXAMGRAIZSSWIH-UHFFFAOYSA-N 0.000 description 2
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- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
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- 239000003607 modifier Substances 0.000 description 1
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- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
- VXRNYQMFDGOGSI-UHFFFAOYSA-N n-(1,3-dihydroxy-2-methylpropan-2-yl)-2-[[1-[(1,3-dihydroxy-2-methylpropan-2-yl)amino]-2-methyl-1-oxopropan-2-yl]diazenyl]-2-methylpropanamide Chemical compound OCC(C)(CO)NC(=O)C(C)(C)N=NC(C)(C)C(=O)NC(C)(CO)CO VXRNYQMFDGOGSI-UHFFFAOYSA-N 0.000 description 1
- YKYONYBAUNKHLG-UHFFFAOYSA-N n-Propyl acetate Natural products CCCOC(C)=O YKYONYBAUNKHLG-UHFFFAOYSA-N 0.000 description 1
- BUGISVZCMXHOHO-UHFFFAOYSA-N n-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]-2-[[1-[[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]amino]-2-methyl-1-oxopropan-2-yl]diazenyl]-2-methylpropanamide Chemical compound OCC(CO)(CO)NC(=O)C(C)(C)N=NC(C)(C)C(=O)NC(CO)(CO)CO BUGISVZCMXHOHO-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- RQAKESSLMFZVMC-UHFFFAOYSA-N n-ethenylacetamide Chemical compound CC(=O)NC=C RQAKESSLMFZVMC-UHFFFAOYSA-N 0.000 description 1
- 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 125000001196 nonadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- QADJHAOXTKCYFT-UHFFFAOYSA-N octyl 3-(3-octoxy-3-oxopropyl)sulfanylpropanoate Chemical compound CCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCC QADJHAOXTKCYFT-UHFFFAOYSA-N 0.000 description 1
- 229940065472 octyl acrylate Drugs 0.000 description 1
- ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
- 150000004866 oxadiazoles Chemical class 0.000 description 1
- 125000003566 oxetanyl group Chemical group 0.000 description 1
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- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
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- 239000002245 particle Substances 0.000 description 1
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- 229910052700 potassium Inorganic materials 0.000 description 1
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- BWJUFXUULUEGMA-UHFFFAOYSA-N propan-2-yl propan-2-yloxycarbonyloxy carbonate Chemical compound CC(C)OC(=O)OOC(=O)OC(C)C BWJUFXUULUEGMA-UHFFFAOYSA-N 0.000 description 1
- QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 description 1
- 229940080818 propionamide Drugs 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940090181 propyl acetate Drugs 0.000 description 1
- LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
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- 150000003335 secondary amines Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 125000002072 seryl group Chemical group 0.000 description 1
- 239000012748 slip agent Substances 0.000 description 1
- WSFQLUVWDKCYSW-UHFFFAOYSA-M sodium;2-hydroxy-3-morpholin-4-ylpropane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(O)CN1CCOCC1 WSFQLUVWDKCYSW-UHFFFAOYSA-M 0.000 description 1
- 229910000679 solder Inorganic materials 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- PFBLRDXPNUJYJM-UHFFFAOYSA-N tert-butyl 2-methylpropaneperoxoate Chemical compound CC(C)C(=O)OOC(C)(C)C PFBLRDXPNUJYJM-UHFFFAOYSA-N 0.000 description 1
- NMOALOSNPWTWRH-UHFFFAOYSA-N tert-butyl 7,7-dimethyloctaneperoxoate Chemical compound CC(C)(C)CCCCCC(=O)OOC(C)(C)C NMOALOSNPWTWRH-UHFFFAOYSA-N 0.000 description 1
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- XTXFUQOLBKQKJU-UHFFFAOYSA-N tert-butylperoxy(trimethyl)silane Chemical compound CC(C)(C)OO[Si](C)(C)C XTXFUQOLBKQKJU-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 150000003585 thioureas Chemical class 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 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
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 239000012780 transparent material Substances 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- XTTGYFREQJCEML-UHFFFAOYSA-N tributyl phosphite Chemical compound CCCCOP(OCCCC)OCCCC XTTGYFREQJCEML-UHFFFAOYSA-N 0.000 description 1
- TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 description 1
- IVIIAEVMQHEPAY-UHFFFAOYSA-N tridodecyl phosphite Chemical compound CCCCCCCCCCCCOP(OCCCCCCCCCCCC)OCCCCCCCCCCCC IVIIAEVMQHEPAY-UHFFFAOYSA-N 0.000 description 1
- BDZBKCUKTQZUTL-UHFFFAOYSA-N triethyl phosphite Chemical compound CCOP(OCC)OCC BDZBKCUKTQZUTL-UHFFFAOYSA-N 0.000 description 1
- RXJKFRMDXUJTEX-UHFFFAOYSA-N triethylphosphine Chemical compound CCP(CC)CC RXJKFRMDXUJTEX-UHFFFAOYSA-N 0.000 description 1
- ILLOBGFGKYTZRO-UHFFFAOYSA-N tris(2-ethylhexyl) phosphite Chemical compound CCCCC(CC)COP(OCC(CC)CCCC)OCC(CC)CCCC ILLOBGFGKYTZRO-UHFFFAOYSA-N 0.000 description 1
- UTAXICGCDMYKKJ-UHFFFAOYSA-N tris(2-ethylhexyl)phosphane Chemical compound CCCCC(CC)CP(CC(CC)CCCC)CC(CC)CCCC UTAXICGCDMYKKJ-UHFFFAOYSA-N 0.000 description 1
- WGKLOLBTFWFKOD-UHFFFAOYSA-N tris(2-nonylphenyl) phosphite Chemical compound CCCCCCCCCC1=CC=CC=C1OP(OC=1C(=CC=CC=1)CCCCCCCCC)OC1=CC=CC=C1CCCCCCCCC WGKLOLBTFWFKOD-UHFFFAOYSA-N 0.000 description 1
- JZNDMMGBXUYFNQ-UHFFFAOYSA-N tris(dodecylsulfanyl)phosphane Chemical compound CCCCCCCCCCCCSP(SCCCCCCCCCCCC)SCCCCCCCCCCCC JZNDMMGBXUYFNQ-UHFFFAOYSA-N 0.000 description 1
- QQBLOZGVRHAYGT-UHFFFAOYSA-N tris-decyl phosphite Chemical compound CCCCCCCCCCOP(OCCCCCCCCCC)OCCCCCCCCCC QQBLOZGVRHAYGT-UHFFFAOYSA-N 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
- 125000003774 valeryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
- 239000001018 xanthene dye Substances 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Chemical class 0.000 description 1
- YZYKBQUWMPUVEN-UHFFFAOYSA-N zafuleptine Chemical compound OC(=O)CCCCCC(C(C)C)NCC1=CC=C(F)C=C1 YZYKBQUWMPUVEN-UHFFFAOYSA-N 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- CHJMFFKHPHCQIJ-UHFFFAOYSA-L zinc;octanoate Chemical compound [Zn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O CHJMFFKHPHCQIJ-UHFFFAOYSA-L 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
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- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/13—Phenols; Phenolates
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- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
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- C08K5/00—Use of organic ingredients
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/37—Thiols
- C08K5/372—Sulfides, e.g. R-(S)x-R'
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- C08K5/51—Phosphorus bound to oxygen
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- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
- C08F220/1811—C10or C11-(Meth)acrylate, e.g. isodecyl (meth)acrylate, isobornyl (meth)acrylate or 2-naphthyl (meth)acrylate
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- C08F222/10—Esters
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Abstract
【解決手段】重合性化合物を安定化させるために用いられる安定化剤組成物であって、(A)セミヒンダードフェノールおよびその二量体からなる群より選ばれた少なくとも1種のセミヒンダードフェノール系化合物と、(B)(チオ)ホスファイト、ホスフィンおよびチオエーテルからなる群より選ばれた少なくとも1種の安定化剤とを含有することを特徴とする安定化剤組成物。
【選択図】なし
Description
(1) 重合性化合物を安定化させるために用いられる安定化剤組成物であって、(A)セミヒンダードフェノールおよびその二量体からなる群より選ばれた少なくとも1種のセミヒンダードフェノール系化合物と、(B)(チオ)ホスファイト、ホスフィンおよびチオエーテルからなる群より選ばれた少なくとも1種の安定化剤とを含有することを特徴とする安定化剤組成物、
(2) α−アリルオキシメチルアクリロイル基を有する重合性エステル化合物を含有する重合性組成物であって、(A)セミヒンダードフェノールおよびその二量体からなる群より選ばれた少なくとも1種のセミヒンダードフェノール系化合物と、(B)(チオ)ホスファイト、ホスフィンおよびチオエーテルからなる群より選ばれた少なくとも1種の安定化剤とを含有することを含有することを特徴とする重合性組成物、および
(3) 前記(2)に記載の重合性組成物を重合させてなる重合体組成物
に関する。
で表わされるセミヒンダードフェノールなどが挙げられる。前記置換基としては、例えば、アリル基、メタリル基、クロチル基、1,1−ジメチル−2−プロペニル基、2−メチル−ブテニル基、3−メチル−2−ブテニル基、3−メチル−3−ブテニル基、2−メチル−3−ブテニル基、オレイル基、リノール基、リノレン基、などの鎖状不飽和炭化水素基;シクロペンチル基、シクロペンチルメチル基、シクロヘキシル基、シクロヘキシルメチル基、4−メチルシクロヘキシル基、4−tert−ブチルシクロヘキシル基、トリシクロデカニル基、イソボルニル基、アダマンチル基、ジシクロペンタニル基、ジシクロペンテニル基などの脂環式炭化水素基;グリシジル基、β−メチルグリシジル基、β−エチルグリシジル基、3,4−エポキシシクロヘキシルメチル基、2−オキセタンメチル基、3−メチル−3−オキセタンメチル基、3−エチル−3−オキセタンメチル基、テトラヒドロフラニル基、テトラヒドロフルフリル基、テトラヒドロピラニル基、ジオキサゾラニル基、ジオキサニル基などの環状エーテル基;フェニル基、メチルフェニル基、ジメチルフェニル基、トリメチルフェニル基、4−tert−ブチルフェニル基、メトキシフェニル基、ヒドロキシフェニル基、ベンジル基、ジフェニルメチル基、ジフェニルエチル基、トリフェニルメチル基、シンナミル基、ナフチル基、アントラニル基などのアリール基;メトキシ基、エトキシ基、メトキシエトキシ基、シクロヘキシルオキシ基、フェノキシ基、フェノキシエトキシ基などのアルコキシ基;ブチルチオ基、オクチルチオ基、ラウリルチオ基、ステアリルチオ基、フェニルチオ基などのアルキルチオ基;アセチル基、プロピオニル基、ブチリル基、バレリル基、ベンゾイル基、トリオイル基、カプロイル基などのアシル基;アセチルオキシ基、プロピオニルオキシ基、ブチリルオキシ基、バレリルオキシ基、ベンゾイルオキシ基、トリオイルオキシ基、カプロイルオキシ基、(メタ)アクリロイルオキシ基などのアシルオキシ基;メトキシカルボニル基、エトキシカルボニル基、ブトキシカルボニル基、オクチルオキシカルボニル基、ラウリルオキシカルボニル基、ステアリルオキシカルボニル基、フェノキシカルボニル基、ベンジルオキシカルボニル基などのアルコキシカルボニル基;ブチルチオカルボニル基、オクチルチオカルボニル基、ラウリルチオカルボニル基、ステアリルチオカルボニル基、フェニルチオカルボニル基、ベンジルチオカルボニル基などのアルキルチオカルボニル基;フッ素原子、塩素原子、臭素原子、ヨウ素原子などのハロゲン原子;ウレイド基;アミド基;シアノ基;水酸基;亜リン酸エステル基;ホスホン酸エステル基;トリメチルシリル基などが挙げられるが、本発明は、かかる例示のみに限定されるものではない。
で表わされるセミヒンダードフェノールの二量体、式(II−b):
で表わされるセミヒンダードフェノールの二量体、式(II−c):
で表わされるセミヒンダードフェノールの二量体などが挙げられる。
で表わされる(チオ)ホスファイトが好ましく、式(III)においてR1、R2およびR3がそれぞれ独立して炭素数が8〜18のアルキル基である(チオ)ホスファイトがより好ましい。なお、R1、R2およびR3のうちの2つの基が結合して環を形成している場合には、環を形成する基の炭素数は5以下であってもよい。
で表わされるチオエーテルが好ましく、式(IV)において、R4およびR5がそれぞれ独立して炭素数が8〜18のアルキル基または炭素数が6〜20のアルコキシカルボニル基で置換された炭素数2〜4のアルキル基であるチオエーテルがより好ましい。チオエーテルのなかでは、取扱い性を向上させる観点から、常温で液状であるチオエーテルが好ましく、化学的安定性を向上させる観点から、長鎖アルキルチオ基を有する(R4およびR5のうち少なくとも1つの基が長鎖アルキル基である)チオエーテルが好ましい。好適な長鎖アルキルチオ基を有するチオエーテルとしては、例えば、(3−ラウリルチオプロピオン酸)ペンタエリスリトールテトラエステル、(3−ラウリルチオプロピオン酸)−4,4’−チオジ(3−メチル−5−tert−ブチル−4−フェノール)エステル、2,4−ビス(オクチルチオメチル)−o−クレゾール、2,4−ビス(ドデシルチオメチル)−o−クレゾールなどが挙げられるが、本発明は、かかる例示のみに限定されるものではない。これらのチオエーテルは、それぞれ単独で用いてもよく、2種類以上を併用してもよい。
で表わされるAMAエステルなどが挙げられる。AMAエステルは、本発明において好適に使用することができる化合物である。
るが、本発明は、かかる例示のみに限定されるものではない。
蒸留塔、相分離器および還流ポンプを備えた5L(リットル)容の丸底フラスコに、α−ヒドロキシメチルアクリル酸メチル1625.7g、アリルアルコール1219.7g(1.5当量)、触媒としてトリエチレンジアミン(DABCO)78.5g(0.05当量)、酸として酢酸84.9g(0.1当量)および酢酸亜鉛二水和物30.7g(0.01当量)、水分の共沸剤としてジイソプロピルエーテル429.1g(0.3当量)、重合禁止剤としてヒドロキノンモノメチルエーテル0.8gおよび4−ヒドロキシ−2,2,6,6−テトラメチルピペリジン−1−オキシル0.8gを仕込んだ。
実施例1−1
セミヒンダードフェノールおよびその二量体からなる群より選ばれた少なくとも1種のセミヒンダードフェノール系化合物に属する安定化剤〔以下、(A)群という〕として、常温(23℃)で液体である6−tert−ブチル−2,4−キシレノール(以下、TPAという)0.03gと、(チオ)ホスファイト、ホスフィンおよびチオエーテルからなる群より選ばれた少なくとも1種の安定化剤に属する安定化剤〔以下、(B)群という〕として、常温(23℃)で液体であるトリフェニルホスファイト(以下、TPPという)0.05gを混合することにより、安定化剤組成物を調製した。
ラジカル重合性組成物2.0g、溶媒としてトルエン、酢酸エチルまたはメチルエチルケトン18.0gを用い、ラジカル重合開始剤として2,2’−アゾビス(2−メチルブチロニトリル)〔日本ファインケム(株)製、商品名:ABN−E(以下、ABN−Eという)〕0.05gを反応容器に入れ、当該反応容器に還流管を取り付け、80℃に保たれた油浴に当該反応容器を浸漬した。時々撹拌しながら反応容器の内容物の温度を80℃に1時間維持した後、反応容器を25℃の水浴に浸漬することにより、反応容器の内容物を冷却した。反応容器の内容物を少量採取し、MeAMAの残存量を以下の方法に基づいて測定し、その結果から重合転化率を求め、ラジカル重合活性の指標とした。なお、重合転化率が高いほどラジカル重合活性に優れている。
MeAMAの残存量は、高速液体クロマトグラフィ(HPLC)装置〔(株)島津製作所製、品番:DGU−20A5、LC−20AD、SIL−20A、SPD−20AおよびCTO−20Aを組み合わせたもの〕を用いて測定した。そのときの測定条件は、以下のとおりである。
・希釈溶媒:アセトニトリル/メタノール=2/1(質量比)
・溶出溶媒:0.1mol%リン酸水溶液/アセトニトリル/メタノール混合溶媒
・分離カラム:(株)資生堂製、商品名:CAPCELL PAK C18 TYPE:AQ
滴下ロート、攪拌機、窒素ガス導入管、温度計および還流冷却管を備えた5L(リットル)容のフラスコに脱イオン水133.0gを仕込んだ。滴下ロートに乳化剤〔花王(株)製、商品名:エマールO〕の25%水溶液16.0g、脱イオン水24.0gおよび前記で得られたラジカル重合性組成物100.0gからなる1段目のプレエマルションを調製した。
安定化剤組成物の種類およびその量を表1に示すように変更したこと以外は、実施例1−1と同様にして安定化剤組成物を調製した。得られた安定化剤組成物を用いて実施例1−1と同様にしてラジカル重合性組成物を得た。得られたラジカル重合性組成物の物性として、ラジカル重合活性および乳化重合におけるラジカル重合活性を実施例1−1と同様にして調べた。その結果を表1に示す。
〔(A)群〕
・ TPA:6−tert−ブチル−2,4−キシレノール(常温で液体)
・ W400:川口化学工業(株)製、商品名:アンテージW−400(セミヒンダードフェノールのo位二量体、常温で固体)
〔(B)群〕
・ TPP:トリフェニルホスファイト(常温で液体)
・ AO412S:(株)ADEKA製、商品名:アデカスタブAO−412S(チオエーテル系安定化剤、常温で固体)
・ AS2112:(株)ADEKA製、商品名:アデカスタブ2112(ホスファイト系安定化剤、常温で固体)
・ PEP36:(株)ADEKA製、商品名:アデカスタブPEP−36(ホスファイト系安定化剤、常温で固体)
・ TPLR:住友化学(株)製、商品名:Sumilizer TPL−R(チオエーテル系安定化剤、常温で固体)
〔その他〕
・ TBHQ:tert−ブチルヒドロキノン(常温で固体)
・ MEHQ:ヒドロキノンモノメチルエーテル(常温で固体)
・ Irg1010:BASFジャパン(株)製、商品名:Irganox1010(ヒンダートフェノール系安定化剤、常温で固体)
〔溶媒〕
・ EAC:酢酸エチル
・ MEK:メチルエチルケトン
実施例2−1
TPA0.03gおよびTPP0.05gを混合することにより、安定化剤組成物を調製した。
ラジカル重合性組成物1.0部と10%水酸化ナトリウム水溶液2.7部とを混合し、得られた溶液を室温下で1時間攪拌した後、目視で溶液の色を確認し、着色レベルおよび色の種類をアルカリ接触時の着色耐性の指標とした。
安定化剤組成物の種類およびその量を表2に示すように変更したこと以外は、実施例2−1と同様にして安定化剤組成物を調製した。得られた安定化剤組成物を用いて実施例2−1と同様にしてラジカル重合性組成物を得た。得られたラジカル重合性組成物の物性として、アルカリ接触時の着色耐性を実施例2−1と同様にして調べた。その結果を表2に示す。
実施例3−1
TPA0.03gおよびTPP0.05gを混合することにより、安定化剤組成物を調製した。
重合体溶液3gを10mL容のスクリュー管に入れ、50℃に加熱した後、モノエタノールアミン0.3gをスクリュー管内に添加し、十分に撹拌し、重合体溶液の色を目視で確認し、着色の有無をアルカリ接触時の着色耐性の指標とした。
10mL容のスクリュー管に前記で得られた重合体溶液5gを入れ、スクリュー管の開口部に蓋をすることによってスクリュー管を密閉し、50℃に保持された熱風乾燥器中で1ヵ月間保管した後、重合体溶液の色を目視で確認し、着色の有無を貯蔵安定性試験条件下における着色耐性の指標とした。
安定化剤組成物の種類およびその量を表3に示すように変更したこと以外は、実施例3−1と同様にして安定化剤組成物を調製した。得られた安定化剤組成物を用いて実施例3−1と同様にして重合体溶液を得た。得られた重合体溶液の物性として、アルカリ接触時の着色耐性および貯蔵安定性試験条件下における着色耐性を実施例3−1と同様にして調べた。その結果を表3に示す。
実施例4−1
TPA0.03gおよびTPP0.05gを混合することにより、安定化剤組成物を調製した。
式差計を用いて前記で得られたフィルム状硬化物の黄色度(b値)を測定し、得られた値を初期b値とした。
試験機:スガ試験機(株)製、商品名:キセノンウェザーメーターX75SC
放射照度:60W/m2
ブラックパネル温度:63℃
湿度:相対湿度50%
試験時間:500時間
安定化剤組成物の種類およびその量を表4に示すように変更したこと以外は、実施例4−1と同様にして安定化剤組成物を調製し、その安定化剤組成物を含むラジカル重合性組成物から得られたフィルム状硬化物の耐候試験条件下における着色耐性を調べた。その結果を表4に示す。
実施例5−1
TPA0.05gおよびTPP0.5gを混合することにより、安定化剤組成物を調製した。
(1)重合物の有無
スクリュー管の内容物(液体)を取り出し、室温(約23℃)下でn−ヘキサンに滴下し、沈殿物が生じなかった場合には、重合物がないと判断し、沈殿物が生じた場合には、重合物があると判断した。ただし、スクリュー管の内容物が明らかに増粘ないしゲル化している場合には、無条件で重合物があると判断した。
内容物をn−ヘキサンに滴下したときから9ヵ月間経過するまでに重合物が生じていない場合には、その内容物の着色状態を目視で観察した。
安定化剤組成物の種類およびその量を表5に示すように変更したこと以外は、実施例5−1と同様にして安定化剤組成物を調製し、その安定化剤組成物を含むラジカル重合性組成物の貯蔵安定性を調べた。その結果を表5に示す。
実施例6−1
TPA0.03gおよびTPP0.1gを混合することにより、安定化剤組成物を調製した。
(1)重合物の有無
重合物の有無は、試験管からその内容物(液体)を取り出し、室温下でn−ヘキサンに滴下し、沈殿物が生じなかった場合には、重合物がないと判断し、沈殿物が生じた場合には、重合物があると判断した。ただし、内容物が明らかに増粘ないしゲル化している場合には、無条件で重合物があると判断した。
重合物が生じていない場合には、内容物の着色状態を目視で観察した。表6の「着色の有無」の欄には、その着色状態を記載した。なお、重合物が生じた場合には、「−」を記載した。
安定化剤組成物の種類およびその量を表6に示すように変更したこと以外は、実施例6−1と同様にして安定化剤組成物を調製し、その安定化剤組成物を含むラジカル重合性組成物の高温安定性(90℃)を調べた。その結果を表6に示す。
実施例7−1
TPA0.05gおよびTPP0.5gを混合することにより、安定化剤組成物を調製した。
安定化剤組成物の種類およびその量を表7に示すように変更したこと以外は、実施例7−1と同様にして安定化剤組成物を調製し、その安定化剤組成物を含むラジカル重合性組成物の高温安定性(110℃)を調べた。その結果を表7に示す。
Claims (3)
- 重合性化合物を安定化させるために用いられる安定化剤組成物であって、(A)セミヒンダードフェノールおよびその二量体からなる群より選ばれた少なくとも1種のセミヒンダードフェノール系化合物と、(B)(チオ)ホスファイト、ホスフィンおよびチオエーテルからなる群より選ばれた少なくとも1種の安定化剤とを含有することを特徴とする安定化剤組成物。
- α−アリルオキシメチルアクリロイル基を有する重合性エステル化合物を含有する重合性組成物であって、(A)セミヒンダードフェノールおよびその二量体からなる群より選ばれた少なくとも1種のセミヒンダードフェノール系化合物と、(B)(チオ)ホスファイト、ホスフィンおよびチオエーテルからなる群より選ばれた少なくとも1種の安定化剤とを含有することを含有することを特徴とする重合性組成物。
- 請求項2に記載の重合性組成物を重合させてなる重合体組成物。
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Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57147545A (en) * | 1981-03-06 | 1982-09-11 | Sumika Color Kk | Preparation of molded polyurethane article |
JPH06220265A (ja) * | 1993-01-28 | 1994-08-09 | Hitachi Cable Ltd | 耐熱性樹脂組成物及び絶縁電線 |
JPH0820711A (ja) * | 1994-07-07 | 1996-01-23 | Nippon Synthetic Chem Ind Co Ltd:The | ポリエーテルエステルブロック共重合体組成物 |
JPH08217892A (ja) * | 1995-02-16 | 1996-08-27 | Teijin Ltd | 再生フイルム |
JP2010016149A (ja) * | 2008-07-03 | 2010-01-21 | Fujifilm Corp | ナノインプリント用硬化性組成物、硬化物およびその製造方法、ならびに液晶表示装置用部材 |
JP2010034513A (ja) * | 2008-07-02 | 2010-02-12 | Fujifilm Corp | インプリント用硬化性組成物、これを用いた硬化物およびその製造方法、並びに、液晶表示装置用部材 |
JP2010254685A (ja) * | 2009-03-31 | 2010-11-11 | Nippon Shokubai Co Ltd | α−(不飽和アルコキシアルキル)アクリレート組成物及びその製造方法 |
Family Cites Families (4)
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Publication number | Priority date | Publication date | Assignee | Title |
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JPH08217892A (ja) * | 1995-02-16 | 1996-08-27 | Teijin Ltd | 再生フイルム |
JP2010034513A (ja) * | 2008-07-02 | 2010-02-12 | Fujifilm Corp | インプリント用硬化性組成物、これを用いた硬化物およびその製造方法、並びに、液晶表示装置用部材 |
JP2010016149A (ja) * | 2008-07-03 | 2010-01-21 | Fujifilm Corp | ナノインプリント用硬化性組成物、硬化物およびその製造方法、ならびに液晶表示装置用部材 |
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CN112449649A (zh) * | 2018-07-23 | 2021-03-05 | 东洋油墨Sc控股株式会社 | 粘着剂及粘着片 |
CN112449649B (zh) * | 2018-07-23 | 2022-10-21 | 东洋油墨Sc控股株式会社 | 粘着剂及粘着片 |
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