JP2013500370A5 - - Google Patents
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- Publication number
- JP2013500370A5 JP2013500370A5 JP2012522156A JP2012522156A JP2013500370A5 JP 2013500370 A5 JP2013500370 A5 JP 2013500370A5 JP 2012522156 A JP2012522156 A JP 2012522156A JP 2012522156 A JP2012522156 A JP 2012522156A JP 2013500370 A5 JP2013500370 A5 JP 2013500370A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- agents
- concentrated aqueous
- polymer dispersion
- phenolic antioxidant
- 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
Links
- 239000004815 dispersion polymer Substances 0.000 claims description 27
- 229920000642 polymer Polymers 0.000 claims description 25
- 239000002530 phenolic antioxidant Substances 0.000 claims description 21
- 239000000178 monomer Substances 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 13
- 239000000843 powder Substances 0.000 claims description 13
- 230000015556 catabolic process Effects 0.000 claims description 11
- 238000006731 degradation reaction Methods 0.000 claims description 11
- 230000003647 oxidation Effects 0.000 claims description 11
- 238000007254 oxidation reaction Methods 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 9
- 239000002245 particle Substances 0.000 claims description 9
- 239000011368 organic material Substances 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 6
- 239000002736 nonionic surfactant Substances 0.000 claims description 6
- 239000003381 stabilizer Substances 0.000 claims description 6
- 239000003945 anionic surfactant Substances 0.000 claims description 5
- 239000003093 cationic surfactant Substances 0.000 claims description 5
- 238000010526 radical polymerization reaction Methods 0.000 claims description 5
- 125000002091 cationic group Chemical group 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 238000006116 polymerization reaction Methods 0.000 claims description 3
- 239000007787 solid Substances 0.000 claims description 3
- 239000011248 coating agent Substances 0.000 claims description 2
- 230000000379 polymerizing effect Effects 0.000 claims description 2
- 230000008016 vaporization Effects 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims 24
- 239000003795 chemical substances by application Substances 0.000 claims 7
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims 6
- -1 alkyl methacrylates Chemical class 0.000 claims 5
- 125000002947 alkylene group Chemical group 0.000 claims 5
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims 4
- 125000004423 acyloxy group Chemical group 0.000 claims 4
- 125000004432 carbon atom Chemical group C* 0.000 claims 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 4
- 239000000654 additive Substances 0.000 claims 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 239000008199 coating composition Substances 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 150000002734 metacrylic acid derivatives Chemical class 0.000 claims 2
- 229910052751 metal Inorganic materials 0.000 claims 2
- 239000002184 metal Substances 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 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 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 1
- ACZGCWSMSTYWDQ-UHFFFAOYSA-N 3h-1-benzofuran-2-one Chemical class C1=CC=C2OC(=O)CC2=C1 ACZGCWSMSTYWDQ-UHFFFAOYSA-N 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 239000006096 absorbing agent Substances 0.000 claims 1
- 239000002318 adhesion promoter Substances 0.000 claims 1
- 150000001298 alcohols Chemical class 0.000 claims 1
- 239000003513 alkali Substances 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000005250 alkyl acrylate group Chemical group 0.000 claims 1
- 125000003282 alkyl amino group Chemical group 0.000 claims 1
- 125000004414 alkyl thio group Chemical group 0.000 claims 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical group [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 239000002518 antifoaming agent Substances 0.000 claims 1
- 239000002216 antistatic agent Substances 0.000 claims 1
- 239000007864 aqueous solution Substances 0.000 claims 1
- 239000011230 binding agent Substances 0.000 claims 1
- 239000003139 biocide Substances 0.000 claims 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical class [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- 238000004581 coalescence Methods 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 230000009849 deactivation Effects 0.000 claims 1
- 239000002270 dispersing agent Substances 0.000 claims 1
- 239000000975 dye Substances 0.000 claims 1
- 239000003995 emulsifying agent Substances 0.000 claims 1
- 239000000945 filler Substances 0.000 claims 1
- 239000003063 flame retardant Substances 0.000 claims 1
- 239000004088 foaming agent Substances 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 1
- 125000005113 hydroxyalkoxy group Chemical group 0.000 claims 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 1
- 150000002443 hydroxylamines Chemical class 0.000 claims 1
- JYGFTBXVXVMTGB-UHFFFAOYSA-N indolin-2-one Chemical class C1=CC=C2NC(=O)CC2=C1 JYGFTBXVXVMTGB-UHFFFAOYSA-N 0.000 claims 1
- 239000000314 lubricant Substances 0.000 claims 1
- 239000006224 matting agent Substances 0.000 claims 1
- 229910044991 metal oxide Inorganic materials 0.000 claims 1
- 150000004706 metal oxides Chemical class 0.000 claims 1
- 239000002667 nucleating agent Substances 0.000 claims 1
- 230000003287 optical effect Effects 0.000 claims 1
- 150000002903 organophosphorus compounds Chemical class 0.000 claims 1
- 150000002978 peroxides Chemical class 0.000 claims 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 claims 1
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical class OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 claims 1
- 239000000049 pigment Substances 0.000 claims 1
- 239000004014 plasticizer Substances 0.000 claims 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 claims 1
- 239000012744 reinforcing agent Substances 0.000 claims 1
- 239000006254 rheological additive Substances 0.000 claims 1
- 238000000518 rheometry Methods 0.000 claims 1
- 239000012748 slip agent Substances 0.000 claims 1
- 125000006850 spacer group Chemical group 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- 239000001993 wax Substances 0.000 claims 1
- 239000000080 wetting agent Substances 0.000 claims 1
- 239000006185 dispersion Substances 0.000 description 7
- 239000004094 surface-active agent Substances 0.000 description 4
- 239000000976 ink Substances 0.000 description 3
- 230000001588 bifunctional effect Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000001804 emulsifying effect Effects 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- GAODDBNJCKQQDY-UHFFFAOYSA-N 2-methyl-4,6-bis(octylsulfanylmethyl)phenol Chemical compound CCCCCCCCSCC1=CC(C)=C(O)C(CSCCCCCCCC)=C1 GAODDBNJCKQQDY-UHFFFAOYSA-N 0.000 description 1
- 0 C*c1nc(*)nc(*)n1 Chemical compound C*c1nc(*)nc(*)n1 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000013011 aqueous formulation Substances 0.000 description 1
- 238000000071 blow moulding Methods 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 238000002296 dynamic light scattering Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000013020 final formulation Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000007641 inkjet printing Methods 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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 true JP2013500370A5 (cg-RX-API-DMAC7.html) | 2013-09-12 |
| JP5797650B2 JP5797650B2 (ja) | 2015-10-21 |
Family
ID=41460219
Family Applications (1)
| 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 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US8580876B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP2459636B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP5797650B2 (cg-RX-API-DMAC7.html) |
| KR (1) | KR20120053018A (cg-RX-API-DMAC7.html) |
| CN (1) | CN102575055B (cg-RX-API-DMAC7.html) |
| WO (1) | WO2011012631A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| PL3087140T3 (pl) | 2013-12-23 | 2020-01-31 | Arlanxeo Singapore Pte. Ltd. | Nowe anty-aglomeranty dla przemysłu kauczukowego |
| US10584195B2 (en) | 2013-12-23 | 2020-03-10 | Arlanxeo Singapore Pte. Ltd. | Ultra pure rubber |
| CN111635595A (zh) | 2013-12-23 | 2020-09-08 | 阿朗新科新加坡私人有限公司 | 高纯度的卤化橡胶 |
| EP3087136B1 (en) | 2013-12-23 | 2019-08-14 | Arlanxeo Singapore Pte. Ltd. | Novel anti-agglomerants for elastomeric ethylene/ -olefin copolymers |
| 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 |
| KR102417286B1 (ko) | 2014-06-30 | 2022-07-05 | 아란세오 싱가포르 프라이빗 리미티드 | 고무 산업용의 신규한 응결방지제 |
| AU2017207981B2 (en) | 2016-01-14 | 2020-10-29 | Isp Investments Llc | Friable shell microcapsules, process for preparing the same and method of use thereof |
| JP7138100B2 (ja) * | 2017-05-11 | 2022-09-15 | 関西ペイント株式会社 | クリヤーコート塗料組成物及び複層塗膜形成方法 |
| WO2019042999A1 (en) * | 2017-09-01 | 2019-03-07 | Basf Se | FORMS OF CONCENTRATED WATER-BASED PRODUCT OF OIL-SOLUBLE ORGANIC UV-ABSORBS |
| 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 |
| GB1489485A (en) | 1974-03-25 | 1977-10-19 | Rohm & Haas | Method for curing polymers |
| 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 |
| MXPA06002754A (es) | 2003-09-11 | 2006-06-14 | Ciba Sc Holding Ag | Formas de producto concentrado basado en agua de estabilizadores de luz elaborados por una tecnica de polimerizacion de heterofase. |
| CN101142242A (zh) * | 2005-03-10 | 2008-03-12 | 巴斯福股份公司 | 包含效应物质的聚合物水分散体、其制备方法和用途 |
| WO2007104713A1 (de) | 2006-03-16 | 2007-09-20 | Basf Se | Effektstoffe enthaltende polymerdispersionen und ihre verwendung |
| JP2009541505A (ja) | 2006-06-20 | 2009-11-26 | ビーエーエスエフ ソシエタス・ヨーロピア | 少なくとも１種の親油性作用物質を含有する水性ポリマー分散液の製造方法及びその使用 |
| BRPI0713466A2 (pt) | 2006-06-27 | 2012-01-24 | Ciba Holding Inc | Absorvedores de uv benzotriazol deslocados por cumprimento de onda longo e seu uso |
| 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 |
-
2010
- 2010-07-27 CN CN201080043240.XA patent/CN102575055B/zh not_active Expired - Fee Related
- 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 US US13/387,246 patent/US8580876B2/en not_active Expired - Fee Related
- 2010-07-27 KR KR1020127005201A patent/KR20120053018A/ko not_active Ceased
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