JP5797650B2 - カプセル封入されたフェノール系酸化防止剤 - Google Patents
カプセル封入されたフェノール系酸化防止剤 Download PDFInfo
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- JP5797650B2 JP5797650B2 JP2012522156A JP2012522156A JP5797650B2 JP 5797650 B2 JP5797650 B2 JP 5797650B2 JP 2012522156 A JP2012522156 A JP 2012522156A JP 2012522156 A JP2012522156 A JP 2012522156A JP 5797650 B2 JP5797650 B2 JP 5797650B2
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- Prior art keywords
- alkyl
- agents
- phenolic antioxidant
- coo
- oco
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- 239000002530 phenolic antioxidant Substances 0.000 title claims description 51
- 125000000217 alkyl group Chemical group 0.000 claims description 98
- -1 substituted - phenyl Chemical group 0.000 claims description 82
- 239000000178 monomer Substances 0.000 claims description 62
- 229920000642 polymer Polymers 0.000 claims description 57
- 239000000203 mixture Substances 0.000 claims description 54
- 239000000843 powder Substances 0.000 claims description 35
- 239000011248 coating agent Substances 0.000 claims description 30
- 239000004815 dispersion polymer Substances 0.000 claims description 29
- 239000002245 particle Substances 0.000 claims description 25
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 24
- 125000002947 alkylene group Chemical group 0.000 claims description 23
- 239000000463 material Substances 0.000 claims description 22
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 22
- 239000007787 solid Substances 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 21
- 238000006116 polymerization reaction Methods 0.000 claims description 20
- 239000003795 chemical substances by application Substances 0.000 claims description 18
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 18
- 239000011230 binding agent Substances 0.000 claims description 17
- 230000015556 catabolic process Effects 0.000 claims description 17
- 238000006731 degradation reaction Methods 0.000 claims description 17
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 17
- 230000003647 oxidation Effects 0.000 claims description 15
- 238000007254 oxidation reaction Methods 0.000 claims description 15
- 125000004423 acyloxy group Chemical group 0.000 claims description 14
- 125000004432 carbon atom Chemical group C* 0.000 claims description 14
- 150000001412 amines Chemical class 0.000 claims description 13
- 239000011368 organic material Substances 0.000 claims description 13
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims description 12
- 229910052799 carbon Inorganic materials 0.000 claims description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims description 12
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 11
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 11
- 239000000654 additive Substances 0.000 claims description 11
- 125000004429 atom Chemical group 0.000 claims description 11
- 239000003381 stabilizer Substances 0.000 claims description 10
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 9
- 125000003545 alkoxy group Chemical group 0.000 claims description 9
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 9
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims description 8
- 125000003282 alkyl amino group Chemical group 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 239000002736 nonionic surfactant Substances 0.000 claims description 8
- 239000003945 anionic surfactant Substances 0.000 claims description 7
- 239000008199 coating composition Substances 0.000 claims description 7
- 150000001298 alcohols Chemical class 0.000 claims description 6
- 239000003513 alkali Substances 0.000 claims description 6
- 125000004414 alkyl thio group Chemical group 0.000 claims description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical group [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 6
- 239000003054 catalyst Substances 0.000 claims description 6
- 239000003093 cationic surfactant Substances 0.000 claims description 6
- 239000000975 dye Substances 0.000 claims description 6
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 6
- 238000010526 radical polymerization reaction Methods 0.000 claims description 6
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims description 5
- 239000003139 biocide Substances 0.000 claims description 5
- 125000002091 cationic group Chemical group 0.000 claims description 5
- 150000002734 metacrylic acid derivatives Chemical class 0.000 claims description 5
- 150000002978 peroxides Chemical class 0.000 claims description 4
- 239000000049 pigment Substances 0.000 claims description 4
- 125000006850 spacer group Chemical group 0.000 claims description 4
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical group CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 claims description 3
- 125000005250 alkyl acrylate group Chemical group 0.000 claims description 3
- 239000002518 antifoaming agent Substances 0.000 claims description 3
- 239000000945 filler Substances 0.000 claims description 3
- 125000005113 hydroxyalkoxy group Chemical group 0.000 claims description 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 3
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 claims description 3
- 230000000379 polymerizing effect Effects 0.000 claims description 3
- 239000006254 rheological additive Substances 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- 230000008016 vaporization Effects 0.000 claims description 3
- 239000001993 wax Substances 0.000 claims description 3
- 239000000080 wetting agent Substances 0.000 claims description 3
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 claims description 2
- ACZGCWSMSTYWDQ-UHFFFAOYSA-N 3h-1-benzofuran-2-one Chemical class C1=CC=C2OC(=O)CC2=C1 ACZGCWSMSTYWDQ-UHFFFAOYSA-N 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 239000006096 absorbing agent Substances 0.000 claims description 2
- 239000002318 adhesion promoter Substances 0.000 claims description 2
- 239000002216 antistatic agent Substances 0.000 claims description 2
- 238000004581 coalescence Methods 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
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- 239000003063 flame retardant Substances 0.000 claims description 2
- 239000004088 foaming agent Substances 0.000 claims description 2
- JYGFTBXVXVMTGB-UHFFFAOYSA-N indolin-2-one Chemical class C1=CC=C2NC(=O)CC2=C1 JYGFTBXVXVMTGB-UHFFFAOYSA-N 0.000 claims description 2
- 239000000314 lubricant Substances 0.000 claims description 2
- 239000006224 matting agent Substances 0.000 claims description 2
- 229910044991 metal oxide Inorganic materials 0.000 claims description 2
- 150000004706 metal oxides Chemical class 0.000 claims description 2
- 239000002667 nucleating agent Substances 0.000 claims description 2
- 150000002903 organophosphorus compounds Chemical class 0.000 claims description 2
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical class OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 claims description 2
- 239000004014 plasticizer Substances 0.000 claims description 2
- 239000012744 reinforcing agent Substances 0.000 claims description 2
- 238000000518 rheometry Methods 0.000 claims description 2
- 239000012748 slip agent Substances 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical class [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 claims 1
- 230000009849 deactivation Effects 0.000 claims 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 1
- 150000002443 hydroxylamines Chemical class 0.000 claims 1
- 230000003287 optical effect Effects 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 42
- 239000006185 dispersion Substances 0.000 description 33
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- 239000003963 antioxidant agent Substances 0.000 description 25
- 150000001875 compounds Chemical class 0.000 description 24
- 238000002296 dynamic light scattering Methods 0.000 description 17
- 229920000728 polyester Polymers 0.000 description 14
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 13
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 13
- 238000009472 formulation Methods 0.000 description 12
- HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 description 12
- 239000000243 solution Substances 0.000 description 12
- 239000004480 active ingredient Substances 0.000 description 11
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical class C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 11
- 229920000647 polyepoxide Polymers 0.000 description 11
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 10
- 239000002253 acid Substances 0.000 description 10
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- 239000003973 paint Substances 0.000 description 10
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- JHWGFJBTMHEZME-UHFFFAOYSA-N 4-prop-2-enoyloxybutyl prop-2-enoate Chemical compound C=CC(=O)OCCCCOC(=O)C=C JHWGFJBTMHEZME-UHFFFAOYSA-N 0.000 description 9
- 239000004971 Cross linker Substances 0.000 description 9
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- 229920000180 alkyd Polymers 0.000 description 9
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- 229910021641 deionized water Inorganic materials 0.000 description 8
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 8
- 239000003999 initiator Substances 0.000 description 8
- 239000000976 ink Substances 0.000 description 8
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- 239000000853 adhesive Substances 0.000 description 7
- 230000001070 adhesive effect Effects 0.000 description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 7
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- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
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- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 6
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- 238000004132 cross linking Methods 0.000 description 6
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- 238000003756 stirring Methods 0.000 description 6
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 5
- 150000001721 carbon Chemical group 0.000 description 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 5
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- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 4
- KUDUQBURMYMBIJ-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC(=O)C=C KUDUQBURMYMBIJ-UHFFFAOYSA-N 0.000 description 4
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- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 4
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- CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical compound OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 description 4
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- QSRJVOOOWGXUDY-UHFFFAOYSA-N 2-[2-[2-[3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoyloxy]ethoxy]ethoxy]ethyl 3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C)=CC(CCC(=O)OCCOCCOCCOC(=O)CCC=2C=C(C(O)=C(C)C=2)C(C)(C)C)=C1 QSRJVOOOWGXUDY-UHFFFAOYSA-N 0.000 description 3
- VFBJXXJYHWLXRM-UHFFFAOYSA-N 2-[2-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]ethylsulfanyl]ethyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCCSCCOC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 VFBJXXJYHWLXRM-UHFFFAOYSA-N 0.000 description 3
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- 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 3
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- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
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- 125000003884 phenylalkyl group Chemical group 0.000 description 1
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- 239000011120 plywood Substances 0.000 description 1
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- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
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- OPQYOFWUFGEMRZ-UHFFFAOYSA-N tert-butyl 2,2-dimethylpropaneperoxoate Chemical compound CC(C)(C)OOC(=O)C(C)(C)C OPQYOFWUFGEMRZ-UHFFFAOYSA-N 0.000 description 1
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- SJMYWORNLPSJQO-UHFFFAOYSA-N tert-butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)(C)C SJMYWORNLPSJQO-UHFFFAOYSA-N 0.000 description 1
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- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
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- 150000003573 thiols Chemical class 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
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- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical class OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
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- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical class [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K9/00—Use of pretreated ingredients
- C08K9/10—Encapsulated ingredients
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/12—Polymerisation in non-solvents
- C08F2/16—Aqueous medium
- C08F2/20—Aqueous medium with the aid of macromolecular dispersing agents
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/44—Polymerisation in the presence of compounding ingredients, e.g. plasticisers, dyestuffs, fillers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- 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
- C08F220/14—Methyl esters, e.g. methyl (meth)acrylate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/005—Stabilisers against oxidation, heat, light, ozone
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- 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
- C08K5/134—Phenols containing ester groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- 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
- C08K5/134—Phenols containing ester groups
- C08K5/1345—Carboxylic esters of phenolcarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/37—Thiols
- C08K5/375—Thiols containing six-membered aromatic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polymerisation Methods In General (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP09166672.7 | 2009-07-29 | ||
| EP09166672 | 2009-07-29 | ||
| PCT/EP2010/060915 WO2011012631A1 (en) | 2009-07-29 | 2010-07-27 | Encapsulated phenolic antioxidants |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013500370A JP2013500370A (ja) | 2013-01-07 |
| JP2013500370A5 JP2013500370A5 (enExample) | 2013-09-12 |
| JP5797650B2 true JP5797650B2 (ja) | 2015-10-21 |
Family
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012522156A Expired - Fee Related JP5797650B2 (ja) | 2009-07-29 | 2010-07-27 | カプセル封入されたフェノール系酸化防止剤 |
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| Country | Link |
|---|---|
| US (1) | US8580876B2 (enExample) |
| EP (1) | EP2459636B1 (enExample) |
| JP (1) | JP5797650B2 (enExample) |
| KR (1) | KR20120053018A (enExample) |
| CN (1) | CN102575055B (enExample) |
| WO (1) | WO2011012631A1 (enExample) |
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| US9144796B1 (en) | 2009-04-01 | 2015-09-29 | Johnson Matthey Public Limited Company | Method of applying washcoat to monolithic substrate |
| US8422923B2 (en) | 2010-08-26 | 2013-04-16 | Xerox Corporation | Phosphate ester polyimide containing intermediate transfer members |
| RU2708245C2 (ru) | 2013-12-23 | 2019-12-05 | Арланксео Сингапур Пте. Лтд. | НОВЫЕ АНТИАГЛОМЕРАТОРЫ ДЛЯ ЭЛАСТОМЕРНЫХ СОПОЛИМЕРОВ ЭТИЛЕНА И α-ОЛЕФИНА |
| US10584195B2 (en) | 2013-12-23 | 2020-03-10 | Arlanxeo Singapore Pte. Ltd. | Ultra pure rubber |
| US10081711B2 (en) | 2013-12-23 | 2018-09-25 | Arlanxeo Singapore Pte. Ltd. | Anti-agglomerants for the rubber industry |
| CA2934725C (en) | 2013-12-23 | 2023-07-25 | Arlanxeo Singapore Pte. Ltd. | Highly pure halogenated rubbers |
| JP5916824B2 (ja) * | 2014-03-31 | 2016-05-11 | 富士フイルム株式会社 | 磁気記録媒体および磁気記録媒体用磁性塗料組成物 |
| WO2016000073A1 (en) | 2014-06-30 | 2016-01-07 | Lanxess Inc. | Novel anti-agglomerants for the rubber industry |
| JP6938514B2 (ja) | 2016-01-14 | 2021-09-22 | アイエスピー インヴェストメンツ エルエルシー | シェルが砕けやすいマイクロカプセル並びにその調整方法及び使用方法 |
| EP3623434A4 (en) * | 2017-05-11 | 2021-08-04 | Kansai Paint Co., Ltd | AQUEOUS COMPOSITION OF TRANSPARENT COATING MATERIAL AND METHOD OF FORMING A MULTI-LAYER COATING FILM |
| CN111050742B (zh) * | 2017-09-01 | 2023-06-30 | 巴斯夫欧洲公司 | 油溶性有机紫外吸收剂的水基浓缩产品形式 |
| CN110183364B (zh) * | 2019-06-27 | 2022-03-29 | 烟台新特路新材料科技有限公司 | 一种硫醚类双酚丙烯酸酯多效抗氧剂及其制备方法 |
| WO2025125201A1 (en) | 2023-12-11 | 2025-06-19 | Basf Se | Aqueous dispersion comprising polymer particles for improving the resistance of waterborne coatings |
| CN119505719B (zh) * | 2025-01-20 | 2025-04-25 | 金华市合丰新材料科技有限公司 | 一种环保型水性胶黏剂及其制备方法 |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1082907B (de) | 1958-09-10 | 1960-06-09 | Basf Ag | Verfahren zur Herstellung von 2, 5-diarylamino-3, 6-dihydro-terephthalsaeureestern |
| US3310545A (en) | 1963-09-11 | 1967-03-21 | Du Pont | Process for curing polychloroprene |
| US3836604A (en) | 1971-06-04 | 1974-09-17 | Bayer Ag | Binders for the electrostatic powder-spraying process |
| US3876578A (en) | 1973-02-08 | 1975-04-08 | Kureha Chemical Ind Co Ltd | Polymer emulsion/dispersion blend compositions for coatings |
| US3880946A (en) | 1973-12-18 | 1975-04-29 | Ford Motor Co | Powder paint compositions including carboxyl terminated polyether crosslinking agent |
| CA1076297A (en) | 1974-03-25 | 1980-04-22 | Graham Swift | Method for curing polymers containing one or more carboxy or anhydride functions |
| US4269749A (en) | 1979-04-30 | 1981-05-26 | The Dow Chemical Company | Method of imparting salt and/or mechanical stability to aqueous polymer microsuspensions |
| US4402983A (en) | 1980-09-19 | 1983-09-06 | E. I. Du Pont De Nemours & Co. | Powder coating composition for automotive topcoat |
| JPS58187464A (ja) | 1982-04-28 | 1983-11-01 | Asahi Chem Ind Co Ltd | 粉体塗料用樹脂組成物 |
| JPH0686560B2 (ja) | 1985-09-30 | 1994-11-02 | 出光石油化学株式会社 | モノビニル芳香族系樹脂組成物の製造方法 |
| EP0256369A3 (en) | 1986-08-04 | 1989-09-13 | The Glidden Company | Glycidyl acrylic powder coatings |
| IT1224640B (it) | 1987-11-20 | 1990-10-18 | Vittorio Ragaini | Procedimento per la realizzazione di reazioni chimiche in sistemi polifasici e relativa apparecchiatura. |
| ITMI992438A1 (it) | 1999-11-23 | 2001-05-23 | Great Lakes Chemical Europ | Miscele stabilizzanti per polimeri organici |
| GB0001752D0 (en) * | 2000-01-27 | 2000-03-15 | Ciba Spec Chem Water Treat Ltd | Particulate compositions and their manufacture |
| WO2005023878A1 (en) | 2003-09-11 | 2005-03-17 | Ciba Specialty Chemicals Holding Inc. | Water based concentrated product forms of light stabilizers made by a heterophase polymerization technique |
| US20080146448A1 (en) | 2005-03-10 | 2008-06-19 | Basf Aktiengesellschaft | Aqueous Polymer Dispersions Comprising Effect Substances, Processes For Preparing Them And Their Use |
| BRPI0709399A2 (pt) | 2006-03-16 | 2011-07-05 | Basf Se | dispersões poliméricas aquosas, pó de polìmero, e, uso de pó de polìmero |
| CA2655864A1 (en) | 2006-06-20 | 2007-12-27 | Basf Se | Method for producing aqueous polymer dispersions containing at least one lipophilic active substance and the use thereof |
| KR101490722B1 (ko) | 2006-06-27 | 2015-02-06 | 시바 홀딩 인크 | 장파장 천이된 벤조트리아졸 ｕｖ-흡수제 및 이의 용도 |
| JP2008101121A (ja) * | 2006-10-19 | 2008-05-01 | Fujifilm Corp | ラテックス組成物およびラテックス組成物の製造方法 |
-
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- 2010-07-27 WO PCT/EP2010/060915 patent/WO2011012631A1/en not_active Ceased
- 2010-07-27 EP EP10737053.8A patent/EP2459636B1/en not_active Not-in-force
- 2010-07-27 JP JP2012522156A patent/JP5797650B2/ja not_active Expired - Fee Related
- 2010-07-27 KR KR1020127005201A patent/KR20120053018A/ko not_active Ceased
- 2010-07-27 CN CN201080043240.XA patent/CN102575055B/zh not_active Expired - Fee Related
- 2010-07-27 US US13/387,246 patent/US8580876B2/en not_active Expired - Fee Related
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| CN102575055B (zh) | 2014-06-18 |
| EP2459636B1 (en) | 2016-01-27 |
| CN102575055A (zh) | 2012-07-11 |
| US8580876B2 (en) | 2013-11-12 |
| KR20120053018A (ko) | 2012-05-24 |
| JP2013500370A (ja) | 2013-01-07 |
| US20120129995A1 (en) | 2012-05-24 |
| WO2011012631A1 (en) | 2011-02-03 |
| EP2459636A1 (en) | 2012-06-06 |
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