JP5160010B2 - 改良されたコーティング及びコーティング組成物 - Google Patents
改良されたコーティング及びコーティング組成物Info
- Publication number
- JP5160010B2 JP5160010B2 JP2002095596A JP2002095596A JP5160010B2 JP 5160010 B2 JP5160010 B2 JP 5160010B2 JP 2002095596 A JP2002095596 A JP 2002095596A JP 2002095596 A JP2002095596 A JP 2002095596A JP 5160010 B2 JP5160010 B2 JP 5160010B2
- Authority
- JP
- Japan
- Prior art keywords
- pnp
- coating
- monomer
- polymer
- pnps
- 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.)
- Expired - Fee Related
Links
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- 238000000034 method Methods 0.000 claims description 39
- 239000002253 acid Substances 0.000 claims description 31
- 238000001035 drying Methods 0.000 claims description 15
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- 229910052710 silicon Inorganic materials 0.000 claims description 11
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- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 7
- 239000010703 silicon Substances 0.000 claims description 7
- 238000011109 contamination Methods 0.000 claims description 6
- 239000002105 nanoparticle Substances 0.000 claims description 5
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- 238000002296 dynamic light scattering Methods 0.000 claims description 2
- 239000000203 mixture Substances 0.000 description 107
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 75
- 229920000642 polymer Polymers 0.000 description 72
- 125000000217 alkyl group Chemical group 0.000 description 37
- 238000006243 chemical reaction Methods 0.000 description 36
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 33
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- BTBJBAZGXNKLQC-UHFFFAOYSA-N ammonium lauryl sulfate Chemical compound [NH4+].CCCCCCCCCCCCOS([O-])(=O)=O BTBJBAZGXNKLQC-UHFFFAOYSA-N 0.000 description 7
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- 238000010557 suspension polymerization reaction Methods 0.000 description 7
- XFCMNSHQOZQILR-UHFFFAOYSA-N 2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOC(=O)C(C)=C XFCMNSHQOZQILR-UHFFFAOYSA-N 0.000 description 6
- AQKYLAIZOGOPAW-UHFFFAOYSA-N 2-methylbutan-2-yl 2,2-dimethylpropaneperoxoate Chemical compound CCC(C)(C)OOC(=O)C(C)(C)C AQKYLAIZOGOPAW-UHFFFAOYSA-N 0.000 description 6
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- 150000001298 alcohols Chemical class 0.000 description 6
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- 239000011521 glass Substances 0.000 description 6
- 125000005843 halogen group Chemical group 0.000 description 6
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- IBDVWXAVKPRHCU-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)ethyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCCOC(=O)C(C)=C IBDVWXAVKPRHCU-UHFFFAOYSA-N 0.000 description 5
- PTTPXKJBFFKCEK-UHFFFAOYSA-N 2-Methyl-4-heptanone Chemical compound CC(C)CC(=O)CC(C)C PTTPXKJBFFKCEK-UHFFFAOYSA-N 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 5
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 5
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 5
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 5
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 5
- INXWLSDYDXPENO-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-[[3-prop-2-enoyloxy-2,2-bis(prop-2-enoyloxymethyl)propoxy]methyl]propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(COC(=O)C=C)(CO)COCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C INXWLSDYDXPENO-UHFFFAOYSA-N 0.000 description 5
- 125000005103 alkyl silyl group Chemical group 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
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- 238000010528 free radical solution polymerization reaction Methods 0.000 description 5
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- 238000010992 reflux Methods 0.000 description 5
- 238000012546 transfer Methods 0.000 description 5
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 5
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 4
- LGJCFVYMIJLQJO-UHFFFAOYSA-N 1-dodecylperoxydodecane Chemical compound CCCCCCCCCCCCOOCCCCCCCCCCCC LGJCFVYMIJLQJO-UHFFFAOYSA-N 0.000 description 4
- KIFPIAKBYOIOCS-UHFFFAOYSA-N 2-methyl-2-(trioxidanyl)propane Chemical compound CC(C)(C)OOO KIFPIAKBYOIOCS-UHFFFAOYSA-N 0.000 description 4
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- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 4
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- 239000001257 hydrogen Substances 0.000 description 4
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- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 3
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 3
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- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 3
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- 241000195493 Cryptophyta Species 0.000 description 3
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 3
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- 238000005191 phase separation Methods 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229940113115 polyethylene glycol 200 Drugs 0.000 description 1
- 229940057847 polyethylene glycol 600 Drugs 0.000 description 1
- 229920005596 polymer binder Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000003361 porogen Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- AXLMPTNTPOWPLT-UHFFFAOYSA-N prop-2-enyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCC=C AXLMPTNTPOWPLT-UHFFFAOYSA-N 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 229940080818 propionamide Drugs 0.000 description 1
- 230000006920 protein precipitation Effects 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000007342 radical addition reaction Methods 0.000 description 1
- 239000012966 redox initiator Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000006254 rheological additive Substances 0.000 description 1
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- 239000000565 sealant Substances 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 210000003802 sputum Anatomy 0.000 description 1
- 208000024794 sputum Diseases 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 238000007655 standard test method Methods 0.000 description 1
- 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 1
- 238000005728 strengthening Methods 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- UFHILTCGAOPTOV-UHFFFAOYSA-N tetrakis(ethenyl)silane Chemical compound C=C[Si](C=C)(C=C)C=C UFHILTCGAOPTOV-UHFFFAOYSA-N 0.000 description 1
- OIUCPPFBFOLPIO-UHFFFAOYSA-N tetratriacontyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C(C)=C OIUCPPFBFOLPIO-UHFFFAOYSA-N 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- KEROTHRUZYBWCY-UHFFFAOYSA-N tridecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCOC(=O)C(C)=C KEROTHRUZYBWCY-UHFFFAOYSA-N 0.000 description 1
- 125000002889 tridecyl group Chemical class [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 1
- PGQNYIRJCLTTOJ-UHFFFAOYSA-N trimethylsilyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)O[Si](C)(C)C PGQNYIRJCLTTOJ-UHFFFAOYSA-N 0.000 description 1
- PKRKCDBTXBGLKV-UHFFFAOYSA-N tris(ethenyl)-methylsilane Chemical compound C=C[Si](C)(C=C)C=C PKRKCDBTXBGLKV-UHFFFAOYSA-N 0.000 description 1
- BNCOGDMUGQWFQE-UHFFFAOYSA-N tris(ethenyl)silicon Chemical compound C=C[Si](C=C)C=C BNCOGDMUGQWFQE-UHFFFAOYSA-N 0.000 description 1
- KRLHYNPADOCLAJ-UHFFFAOYSA-N undecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCOC(=O)C(C)=C KRLHYNPADOCLAJ-UHFFFAOYSA-N 0.000 description 1
- 238000007738 vacuum evaporation Methods 0.000 description 1
- UIYCHXAGWOYNNA-UHFFFAOYSA-N vinyl sulfide Chemical compound C=CSC=C UIYCHXAGWOYNNA-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 230000003442 weekly effect Effects 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 239000008096 xylene Substances 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
- 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S526/909—Polymerization characterized by particle size of product
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/25—Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
- Y10T428/254—Polymeric or resinous material
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymerisation Methods In General (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US28029701P | 2001-03-30 | 2001-03-30 | |
| US60/280297 | 2001-03-30 | ||
| US10/097,256 US6939922B2 (en) | 2001-03-30 | 2002-03-15 | Coating and coating composition |
| US10/097256 | 2002-03-15 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010150149A Division JP2010270334A (ja) | 2001-03-30 | 2010-06-30 | 改良されたコーティング及びコーティング組成物 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2003027009A JP2003027009A (ja) | 2003-01-29 |
| JP2003027009A5 JP2003027009A5 (enExample) | 2008-04-17 |
| JP5160010B2 true JP5160010B2 (ja) | 2013-03-13 |
Family
ID=26793040
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002095596A Expired - Fee Related JP5160010B2 (ja) | 2001-03-30 | 2002-03-29 | 改良されたコーティング及びコーティング組成物 |
| JP2010150149A Ceased JP2010270334A (ja) | 2001-03-30 | 2010-06-30 | 改良されたコーティング及びコーティング組成物 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010150149A Ceased JP2010270334A (ja) | 2001-03-30 | 2010-06-30 | 改良されたコーティング及びコーティング組成物 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US6939922B2 (enExample) |
| EP (1) | EP1245587B1 (enExample) |
| JP (2) | JP5160010B2 (enExample) |
| AU (1) | AU785160B2 (enExample) |
| DE (1) | DE60207627T2 (enExample) |
| MX (1) | MXPA02003170A (enExample) |
Families Citing this family (58)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6939922B2 (en) * | 2001-03-30 | 2005-09-06 | Rohm And Haas Company | Coating and coating composition |
| US6767978B2 (en) * | 2002-01-03 | 2004-07-27 | Atofina Chemicals, Inc. | Copolymers containing fluoro and silyl groups and their use in marine antifoulant composition |
| EP1371685A3 (en) * | 2002-06-14 | 2004-01-07 | Rohm And Haas Company | Aqueous polymeric composition containing polymeric nanoparticles and treatments prepared therefrom |
| US20030232916A1 (en) * | 2002-06-14 | 2003-12-18 | Lorah Dennis Paul | Nonaqueous compositions |
| EP1371698A1 (en) * | 2002-06-14 | 2003-12-17 | Rohm And Haas Company | Polymeric nanoparticle formulations and their use as cement sealers |
| EP1371694B1 (en) * | 2002-06-14 | 2010-03-03 | Rohm And Haas Company | Polymeric nanoparticle formulations and their use for improving the dirt pick up resistance of a coating |
| EP1371718A1 (en) * | 2002-06-14 | 2003-12-17 | Rohm And Haas Company | Polymeric nanoparticle formulations and their use as fabric care additives |
| US7091275B1 (en) * | 2002-06-14 | 2006-08-15 | Rohm And Haas Company | Aqueous polymeric composition containing polymeric nanoparticles and treatments prepared therefrom |
| US9051419B2 (en) * | 2002-06-14 | 2015-06-09 | Richard H. Hall | Polymer |
| US7244784B2 (en) * | 2002-06-14 | 2007-07-17 | Rohm And Haas Company | Aqueous nanoparticle dispersions |
| AU2003204606A1 (en) * | 2002-06-14 | 2004-01-15 | Rohm And Haas Company | Water-based adhesives |
| DE60320177T2 (de) * | 2002-06-14 | 2009-04-09 | Rohm And Haas Co. | Wässrige Zusammensetzung, welche Polymernanoteilchen enthält |
| EP1371693A3 (en) * | 2002-06-14 | 2004-01-07 | Rohm And Haas Company | Damage resistant coatings, films and articles of manufacture containing crosslinked nanoparticles |
| EP1371699A3 (en) * | 2002-06-14 | 2004-01-14 | Rohm And Haas Company | Polymeric nanoparticle and antimicrobial coating formulations |
| CN1325580C (zh) | 2002-09-30 | 2007-07-11 | 罗姆和哈斯公司 | 聚合纳米颗粒配方及其在改进涂层的抗积尘性方面的应用 |
| CN1225515C (zh) * | 2002-09-30 | 2005-11-02 | 罗姆和哈斯公司 | 含有交联的纳米颗粒的耐破损涂层、薄膜和制品 |
| EP1403332A1 (en) * | 2002-09-30 | 2004-03-31 | Rohm And Haas Company | Nonaqueous compositions comprising polymernanoparticles (PNP) |
| US20040063809A1 (en) * | 2002-09-30 | 2004-04-01 | Zhenwen Fu | Polymeric binders for inkjet inks |
| US7009003B2 (en) * | 2002-09-30 | 2006-03-07 | Rohm And Haas Company | Plastic composition |
| EP1411076A1 (en) * | 2002-10-15 | 2004-04-21 | Rohm And Haas Company | Continuous production of crosslinked polymer nanoparticles |
| DE10248879A1 (de) * | 2002-10-18 | 2004-04-29 | Basf Ag | Alkyldiketene enthaltende wässrige Polymerdispersionen, Verfahren zu ihrer Herstellung und ihre Verwendung |
| EP1419893A1 (en) * | 2002-11-18 | 2004-05-19 | Agfa-Gevaert | Improved ink jet recording material |
| MXPA05008247A (es) * | 2003-02-07 | 2005-10-05 | Surface Specialties Sa | Dispersion polimerica acuosa y proceso. |
| EP1447074A3 (en) * | 2003-02-12 | 2004-10-13 | Rohm And Haas Company | Polymeric nanoparticles in consumer products |
| IL157437A0 (en) * | 2003-07-14 | 2004-03-28 | Superseal Ltd Superseal Ltd | Hydrophobic aggregate and applications thereof |
| US6893783B2 (en) * | 2003-10-08 | 2005-05-17 | Kodak Polychrome Graphics Lld | Multilayer imageable elements |
| US8153730B2 (en) * | 2003-11-26 | 2012-04-10 | Fina Technology, Inc. | Polyolefin blends used as masterbatch concentrates |
| US20050181000A1 (en) * | 2004-02-17 | 2005-08-18 | Lundquist Eric G. | Polymeric nanoparticles in consumer products |
| US7758788B2 (en) * | 2004-08-13 | 2010-07-20 | Mentor Worldwide Llc | Spray method for forming shells for prostheses |
| DE102005017327B4 (de) * | 2005-04-14 | 2007-08-30 | EKATO Rühr- und Mischtechnik GmbH | Bearbeitungsanlage |
| GB2427868A (en) * | 2005-07-04 | 2007-01-10 | Samuel Michael Baker | Cellulosic products having oleophobic and hydrophobic properties |
| US20070037942A1 (en) * | 2005-07-07 | 2007-02-15 | Janos Borbely | Preparation of reactive polymeric nanoparticles |
| EP1904590B1 (en) * | 2005-07-15 | 2015-12-30 | Chroma Australia Pty Limited | Paint composition |
| DE102005044520A1 (de) * | 2005-09-16 | 2007-03-22 | Basf Ag | Verfahren zur Behandlung von Oberflächen |
| US8030376B2 (en) | 2006-07-12 | 2011-10-04 | Minusnine Technologies, Inc. | Processes for dispersing substances and preparing composite materials |
| EP1923504A1 (en) * | 2006-11-20 | 2008-05-21 | Rohm and Haas France SAS | Coated paper and paperboard |
| ATE542841T1 (de) * | 2006-12-12 | 2012-02-15 | Unilever Nv | Polymere |
| US20100183540A1 (en) * | 2007-07-06 | 2010-07-22 | Jotun A/S | Branched polymer and antifouling coating composition comprising the polymer |
| US8551463B2 (en) * | 2007-10-22 | 2013-10-08 | Living Proof, Inc. | Hair care compositions and methods of treating hair |
| US8226934B2 (en) | 2007-10-22 | 2012-07-24 | Living Proof, Inc. | Hair care compositions and methods of treating hair using same |
| US8034871B2 (en) * | 2008-03-05 | 2011-10-11 | Columbia Insurance Company | Latex based open-time extenders for low VOC paints |
| EP2166057B1 (de) | 2008-08-26 | 2011-12-28 | Basf Se | Klebstoffzusammensetzung für selbstklebende, wiederablösbare Artikel auf Basis von adhäsiven Polymeren und organischen Nanopartikeln |
| US8580894B2 (en) * | 2008-10-10 | 2013-11-12 | Incoat Llc | Two part, low molecular weight self curing, low viscosity acrylic penetrant, sealant and coating composition, and methods for using the same |
| JP5734858B2 (ja) * | 2008-10-24 | 2015-06-17 | ソルベイ・アドバンスト・ポリマーズ・エルエルシー | 高純度ジフェニルスルホン、調製、およびポリ(アリールエーテルケトン)の調製のためのその使用 |
| US7887992B2 (en) * | 2008-12-23 | 2011-02-15 | E. I. Du Pont De Nemours And Company | Photosensitive paste and process for production of pattern using the same |
| JP2011046854A (ja) * | 2009-08-28 | 2011-03-10 | Kikusui Chemical Industries Co Ltd | 光硬化性塗料 |
| CN102181254B (zh) * | 2010-03-03 | 2015-08-12 | 武汉市科达云石护理材料有限公司 | 增韧云石胶组合物 |
| PL2563872T3 (pl) * | 2010-04-28 | 2015-08-31 | Gcp Applied Tech Inc | Membrana impregnująca |
| US8931228B2 (en) * | 2010-04-28 | 2015-01-13 | W. R. Grace & Co.-Conn. | Waterproofing membrane |
| WO2011139692A1 (en) | 2010-04-28 | 2011-11-10 | W.R. Grace & Co.-Conn. | Waterproofing membrane |
| WO2014111292A1 (en) | 2013-01-18 | 2014-07-24 | Basf Se | Acrylic dispersion-based coating compositions |
| BR112018007933B1 (pt) | 2015-10-19 | 2021-11-23 | Kao Corporation | Método de formação de revestimento para formar um revestimento em uma superfície da pele |
| SG11201803182QA (en) * | 2015-10-19 | 2018-05-30 | Kao Corp | Method for producing coating film |
| CN105462428B (zh) * | 2015-11-25 | 2018-06-26 | 三棵树涂料股份有限公司 | 一种高效耐水水性建筑涂料乳液聚合物及其制备方法 |
| EP3394139B1 (de) * | 2015-12-21 | 2022-07-20 | Sika Technology AG | Polyurethanzusammensetzung mit geringer weichmachermigration |
| KR20220058562A (ko) * | 2019-08-30 | 2022-05-09 | 다우 글로벌 테크놀로지스 엘엘씨 | 아크릴레이트-실록산 공중합체 입자의 수성 분산액 |
| KR20220131282A (ko) | 2020-01-22 | 2022-09-27 | 다우 글로벌 테크놀로지스 엘엘씨 | 실리콘-아크릴레이트 공중합체, 및 관련 방법 및 조성물 |
| JP7075533B1 (ja) * | 2021-09-29 | 2022-05-25 | 大日精化工業株式会社 | 活性エネルギー線硬化型インキ組成物及び印刷物 |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3841699A1 (de) * | 1987-12-17 | 1989-06-29 | Nippon Zeon Co | Thermoplastische elastomerzusammensetzung |
| CA2006930C (en) | 1988-12-29 | 1996-10-22 | Tasaburo Ueno | Powder coatings |
| US5212273A (en) | 1991-06-20 | 1993-05-18 | Ppg Industries, Inc. | Crosslinked polymeric microparticles; their method of preparation and use in coating compositions |
| FR2691969B1 (fr) | 1992-06-04 | 1994-09-23 | Prolabo Sa | Nanoparticules de polymères fonctionnalisées, leur procédé de préparation et leur utilisation. |
| US5756573A (en) * | 1995-10-05 | 1998-05-26 | Sc Johnson Commerical Markets, Inc. | Seed polymerized latex polymer having a gradient polymeric morphology and process for preparing the same |
| DE19624280A1 (de) * | 1996-06-18 | 1998-01-02 | Basf Ag | Verfahren zur Herstellung niedrigviskoser, wässriger Polymerisatdispersionen mit Polymervolumenkonzentrationen von wenigstens 50 Vol.-% |
| US5874111A (en) * | 1997-01-07 | 1999-02-23 | Maitra; Amarnath | Process for the preparation of highly monodispersed polymeric hydrophilic nanoparticles |
| US6130014A (en) * | 1999-07-15 | 2000-10-10 | Eastman Kodak Company | Overcoat material as protecting layer for image recording materials |
| AU770696B2 (en) | 1999-07-30 | 2004-02-26 | Ppg Industries Ohio, Inc. | Cured coatings having improved scratch resistance, coated substrates and methods related thereto |
| US6903175B2 (en) * | 2001-03-26 | 2005-06-07 | Shipley Company, L.L.C. | Polymer synthesis and films therefrom |
| US6852800B2 (en) * | 2001-03-30 | 2005-02-08 | Rohm And Haas Company | Plastic composition |
| US6939922B2 (en) * | 2001-03-30 | 2005-09-06 | Rohm And Haas Company | Coating and coating composition |
| US7189767B2 (en) * | 2001-03-30 | 2007-03-13 | Rohm And Haas Company | Colorants, dispersants, dispersions, and inks |
| US20030232916A1 (en) * | 2002-06-14 | 2003-12-18 | Lorah Dennis Paul | Nonaqueous compositions |
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2002
- 2002-03-15 US US10/097,256 patent/US6939922B2/en not_active Expired - Lifetime
- 2002-03-26 MX MXPA02003170A patent/MXPA02003170A/es unknown
- 2002-03-27 DE DE60207627T patent/DE60207627T2/de not_active Expired - Lifetime
- 2002-03-27 AU AU29188/02A patent/AU785160B2/en not_active Ceased
- 2002-03-27 EP EP02252202A patent/EP1245587B1/en not_active Expired - Lifetime
- 2002-03-29 JP JP2002095596A patent/JP5160010B2/ja not_active Expired - Fee Related
-
2010
- 2010-06-30 JP JP2010150149A patent/JP2010270334A/ja not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| AU2918802A (en) | 2002-10-03 |
| JP2003027009A (ja) | 2003-01-29 |
| US20030059599A1 (en) | 2003-03-27 |
| US6939922B2 (en) | 2005-09-06 |
| EP1245587B1 (en) | 2005-11-30 |
| JP2010270334A (ja) | 2010-12-02 |
| DE60207627T2 (de) | 2006-08-10 |
| DE60207627D1 (de) | 2006-01-05 |
| AU785160B2 (en) | 2006-10-05 |
| MXPA02003170A (es) | 2002-11-05 |
| EP1245587A1 (en) | 2002-10-02 |
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