JP2013500370A5 - - Google Patents
Download PDFInfo
- 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 (enExample) | 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 (enExample) |
| EP (1) | EP2459636B1 (enExample) |
| JP (1) | JP5797650B2 (enExample) |
| KR (1) | KR20120053018A (enExample) |
| CN (1) | CN102575055B (enExample) |
| WO (1) | WO2011012631A1 (enExample) |
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 |
| 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 |
-
2010
- 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
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2013500370A5 (enExample) | ||
| US7119133B2 (en) | Latex-encapsulated particulates for ink-jet applications | |
| JP4511516B2 (ja) | 反応性界面活性剤が固定化されたインクジェットラテックス | |
| JP5582524B2 (ja) | 有機ナノ粒子の調製方法 | |
| JP5797650B2 (ja) | カプセル封入されたフェノール系酸化防止剤 | |
| TWI320790B (en) | Latex-based overcoat for ink-jet printing applications | |
| US7402617B2 (en) | Low bulk density, low surface dielectric constant latex polymers for ink-jet ink applications | |
| JP2009541554A (ja) | 異相重合技術によって作製された光開始剤の水ベースの濃縮されたプロダクト形態 | |
| EP1756237A1 (en) | Latex-encapsulated particulates for ink-jet applications | |
| JP2015157893A (ja) | インドレニン化合物 | |
| WO2016076116A1 (ja) | 水系樹脂分散体および塗料 | |
| US20130065996A1 (en) | Pigment Particles Containing a Vinyl Group and Encapsulated by a Cross-linked Polymer | |
| JP4521307B2 (ja) | インクジェット記録用水系インク | |
| JP5828655B2 (ja) | 塗料用樹脂組成物 | |
| JP3442170B2 (ja) | アクリル水性分散体用造膜助剤及びその製法 | |
| JP4049600B2 (ja) | 造膜助剤及びこれを含有する水性組成物 | |
| JP2007131817A (ja) | 顔料分散体の製造方法。 | |
| JP5545346B2 (ja) | 有機過酸化物を含有する懸濁重合トナー製造用の重合性単量体組成物、懸濁重合組成物、及び懸濁重合物 | |
| WO2020035124A1 (en) | Surface active adjuvant for coatings | |
| JP7056156B2 (ja) | インク及び画像形成方法 | |
| JP2005200514A (ja) | 改質天然ゴムラテックス組成物 | |
| JP2020070322A (ja) | 着色樹脂粒子の水分散体、インクジェットインク、及び着色樹脂粒子の水分散体の製造方法 |