FI58926C - Vattenhaltig polymeremulsion anvaendbar som skydds- och dekorationsbelaeggning samt som lim och foerfarande foer framstaellning av denna - Google Patents
Vattenhaltig polymeremulsion anvaendbar som skydds- och dekorationsbelaeggning samt som lim och foerfarande foer framstaellning av denna Download PDFInfo
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- FI58926C FI58926C FI751929A FI751929A FI58926C FI 58926 C FI58926 C FI 58926C FI 751929 A FI751929 A FI 751929A FI 751929 A FI751929 A FI 751929A FI 58926 C FI58926 C FI 58926C
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- monomer
- cellulose ester
- particles
- polymer
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- 101100148710 Clarkia breweri SAMT gene Proteins 0.000 title 1
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- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 claims description 6
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- 150000004074 biphenyls Chemical class 0.000 description 1
- CMCJNODIWQEOAI-UHFFFAOYSA-N bis(2-butoxyethyl)phthalate Chemical compound CCCCOCCOC(=O)C1=CC=CC=C1C(=O)OCCOCCCC CMCJNODIWQEOAI-UHFFFAOYSA-N 0.000 description 1
- ONZOGXRINCURBP-NXEZZACHSA-N bis(2-methylpropyl) (2r,3r)-2,3-dihydroxybutanedioate Chemical compound CC(C)COC(=O)[C@H](O)[C@@H](O)C(=O)OCC(C)C ONZOGXRINCURBP-NXEZZACHSA-N 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- SHZIWNPUGXLXDT-UHFFFAOYSA-N caproic acid ethyl ester Natural products CCCCCC(=O)OCC SHZIWNPUGXLXDT-UHFFFAOYSA-N 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 239000000679 carrageenan Substances 0.000 description 1
- 235000010418 carrageenan Nutrition 0.000 description 1
- 229920001525 carrageenan Polymers 0.000 description 1
- 229940113118 carrageenan Drugs 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 230000035602 clotting Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 1
- 229960001826 dimethylphthalate Drugs 0.000 description 1
- DWNAQMUDCDVSLT-UHFFFAOYSA-N diphenyl phthalate Chemical compound C=1C=CC=C(C(=O)OC=2C=CC=CC=2)C=1C(=O)OC1=CC=CC=C1 DWNAQMUDCDVSLT-UHFFFAOYSA-N 0.000 description 1
- WBZKQQHYRPRKNJ-UHFFFAOYSA-L disulfite Chemical compound [O-]S(=O)S([O-])(=O)=O WBZKQQHYRPRKNJ-UHFFFAOYSA-L 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000005755 formation reaction Methods 0.000 description 1
- FATAVLOOLIRUNA-UHFFFAOYSA-N formylmethyl Chemical group [CH2]C=O FATAVLOOLIRUNA-UHFFFAOYSA-N 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 description 1
- 239000001087 glyceryl triacetate Substances 0.000 description 1
- 235000013773 glyceryl triacetate Nutrition 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229920006270 hydrocarbon resin Polymers 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 159000000014 iron salts Chemical class 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000000693 micelle Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- DKYVVNLWACXMDW-UHFFFAOYSA-N n-cyclohexyl-4-methylbenzenesulfonamide Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC1CCCCC1 DKYVVNLWACXMDW-UHFFFAOYSA-N 0.000 description 1
- OHPZPBNDOVQJMH-UHFFFAOYSA-N n-ethyl-4-methylbenzenesulfonamide Chemical compound CCNS(=O)(=O)C1=CC=C(C)C=C1 OHPZPBNDOVQJMH-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl 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])[H] 0.000 description 1
- UYDLBVPAAFVANX-UHFFFAOYSA-N octylphenoxy polyethoxyethanol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(OCCOCCOCCOCCO)C=C1 UYDLBVPAAFVANX-UHFFFAOYSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 150000002889 oleic acids Chemical class 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical class [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 125000001557 phthalyl group Chemical group C(=O)(O)C1=C(C(=O)*)C=CC=C1 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001983 poloxamer Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 235000019394 potassium persulphate Nutrition 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- VEYCPJGKKJULEP-UHFFFAOYSA-N prop-2-enoic acid sulfuric acid Chemical compound OC(=O)C=C.OS(O)(=O)=O VEYCPJGKKJULEP-UHFFFAOYSA-N 0.000 description 1
- ARENMZZMCSLORU-UHFFFAOYSA-N propan-2-yl naphthalene-1-sulfonate Chemical class C1=CC=C2C(S(=O)(=O)OC(C)C)=CC=CC2=C1 ARENMZZMCSLORU-UHFFFAOYSA-N 0.000 description 1
- 229940070891 pyridium Drugs 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229940043230 sarcosine Drugs 0.000 description 1
- 229920006126 semicrystalline polymer Polymers 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- VYGBQXDNOUHIBZ-UHFFFAOYSA-L sodium formaldehyde sulphoxylate Chemical class [Na+].[Na+].O=C.[O-]S[O-] VYGBQXDNOUHIBZ-UHFFFAOYSA-L 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 1
- FCZYGJBVLGLYQU-UHFFFAOYSA-M sodium;2-[2-[2-[4-(2,4,4-trimethylpentan-2-yl)phenoxy]ethoxy]ethoxy]ethanesulfonate Chemical compound [Na+].CC(C)(C)CC(C)(C)C1=CC=C(OCCOCCOCCS([O-])(=O)=O)C=C1 FCZYGJBVLGLYQU-UHFFFAOYSA-M 0.000 description 1
- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
- 239000001587 sorbitan monostearate Substances 0.000 description 1
- 235000011076 sorbitan monostearate Nutrition 0.000 description 1
- 229940035048 sorbitan monostearate Drugs 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 229940117986 sulfobetaine Drugs 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- PZTAGFCBNDBBFZ-UHFFFAOYSA-N tert-butyl 2-(hydroxymethyl)piperidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCCCC1CO PZTAGFCBNDBBFZ-UHFFFAOYSA-N 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 description 1
- LMYRWZFENFIFIT-UHFFFAOYSA-N toluene-4-sulfonamide Chemical class CC1=CC=C(S(N)(=O)=O)C=C1 LMYRWZFENFIFIT-UHFFFAOYSA-N 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 235000010487 tragacanth Nutrition 0.000 description 1
- 229940116362 tragacanth Drugs 0.000 description 1
- 229960002622 triacetin Drugs 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
- WTLBZVNBAKMVDP-UHFFFAOYSA-N tris(2-butoxyethyl) phosphate Chemical compound CCCCOCCOP(=O)(OCCOCCCC)OCCOCCCC WTLBZVNBAKMVDP-UHFFFAOYSA-N 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 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
- C08F291/00—Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds according to more than one of the groups C08F251/00 - C08F289/00
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polymerisation Methods In General (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US48527174 | 1974-07-02 | ||
| US05/485,271 US3953386A (en) | 1974-07-02 | 1974-07-02 | Aqueous emulsions containing homogeneous particles of cellulosic ester/acrylic polymers |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI751929A FI751929A (xx) | 1976-01-03 |
| FI58926B FI58926B (fi) | 1981-01-30 |
| FI58926C true FI58926C (fi) | 1981-05-11 |
Family
ID=23927527
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI751929A FI58926C (fi) | 1974-07-02 | 1975-07-01 | Vattenhaltig polymeremulsion anvaendbar som skydds- och dekorationsbelaeggning samt som lim och foerfarande foer framstaellning av denna |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US3953386A (xx) |
| JP (1) | JPS5917123B2 (xx) |
| BE (1) | BE830871A (xx) |
| BR (1) | BR7504131A (xx) |
| CA (1) | CA1052487A (xx) |
| CH (1) | CH601385A5 (xx) |
| DE (1) | DE2529547C2 (xx) |
| FI (1) | FI58926C (xx) |
| FR (1) | FR2277101A1 (xx) |
| GB (1) | GB1515723A (xx) |
| IT (1) | IT1039618B (xx) |
| NL (1) | NL183191C (xx) |
| NO (1) | NO147071C (xx) |
| PH (1) | PH12452A (xx) |
| SE (1) | SE416209B (xx) |
| ZA (1) | ZA754214B (xx) |
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4134809A (en) * | 1977-08-22 | 1979-01-16 | Eastman Kodak Company | Radiation curable cellulose ester-acrylate compositions |
| JPS5554301A (en) * | 1978-10-17 | 1980-04-21 | Daicel Chem Ind Ltd | Preparation of aqueous dispersion of synthetic resin solubilized with cellulose acetate alkylate |
| JPS5676422A (en) * | 1979-11-29 | 1981-06-24 | Kansai Paint Co Ltd | Cellulose derivative-containing, oxidation-curable emulsion composition |
| US4352902A (en) * | 1980-01-08 | 1982-10-05 | Kansai Paint Co., Ltd. | Emulsion composition containing cellulose derivative |
| DE3007936A1 (de) * | 1980-03-01 | 1981-09-24 | Bayer Ag, 5090 Leverkusen | Waessrige dispersionen |
| BR8108666A (pt) * | 1980-07-03 | 1982-05-25 | Dulux Australia Ltd | Processo de dispersao e prodoto |
| EP0094386B1 (en) * | 1981-06-29 | 1986-03-05 | Dulux Australia Ltd | Stable aqueous film-forming dispersions |
| IE52863B1 (en) * | 1981-07-06 | 1988-03-30 | Dulux Australia Ltd | Polymer dispersions |
| EP0070023B1 (en) * | 1981-07-15 | 1987-09-30 | Nippon Oil Co. Ltd. | Process for producing water-insoluble polymers of uniform shape |
| JPS5823847A (ja) | 1981-08-04 | 1983-02-12 | Kansai Paint Co Ltd | 繊維素誘導体含有エマルシヨン組成物 |
| FR2515657B1 (fr) * | 1981-11-03 | 1987-07-17 | Kendall & Co | Procede de polymerisation en emulsion et produit obtenu |
| JPS5958069A (ja) * | 1982-09-27 | 1984-04-03 | Hoechst Gosei Kk | 強接着性エマルジヨン型粘着剤 |
| JPS60195172A (ja) * | 1984-03-16 | 1985-10-03 | Dainippon Ink & Chem Inc | セルロ−ス誘導体含有ビニル系共重合体の水性分散物およびその製造法 |
| JPS61166809A (ja) * | 1985-01-19 | 1986-07-28 | Hayashikane Zosen Kk | 高吸水性樹脂粉粒体の製造方法 |
| US4687594A (en) * | 1985-05-10 | 1987-08-18 | Stepan Company | Emulsifiers useful in the manufacture of high solids emulsion polymers |
| US4814015A (en) * | 1987-08-07 | 1989-03-21 | Prillaman Chemical Corporation | Waterborne nitrocellulose compositions |
| DE3814284A1 (de) * | 1988-04-28 | 1989-11-09 | Wolff Walsrode Ag | Waessrige celluloseesterdispersionen und ihre herstellung |
| US5216065A (en) * | 1990-11-29 | 1993-06-01 | The Mead Corporation | Emulsion polymerization with large particle size |
| US5143970A (en) * | 1991-01-07 | 1992-09-01 | Aqualon Company | Process for making nitrocellulose-acrylic latices |
| US5705467A (en) * | 1991-10-22 | 1998-01-06 | Choy; Clement K. | Thickened aqueous cleaning compositions and methods of use |
| US6048611A (en) * | 1992-02-03 | 2000-04-11 | 3M Innovative Properties Company | High solids moisture resistant latex pressure-sensitive adhesive |
| US5677374A (en) * | 1992-04-16 | 1997-10-14 | Raisio Chemicals Oy | Thickening agent comprising aqueous dispersion of graft-copolymerized starch |
| US5470906A (en) * | 1993-12-27 | 1995-11-28 | The Glidden Company | Odor free, air dry, decorative latex paints |
| CA2204242A1 (en) * | 1994-11-03 | 1996-05-17 | Bernardus J.W. Janssen | Cellulose ethers in emulsion polymerization dispersions |
| US6046259A (en) * | 1996-06-27 | 2000-04-04 | Ppg Industries Ohio, Inc. | Stable aqueous dispersions of cellulose esters and their use in coatings |
| US6197479B1 (en) * | 1998-06-26 | 2001-03-06 | Toray Industries, Inc. | Photosensitive resin composition, method for producing photosensitive resin composition, and printing plate material |
| US6624222B2 (en) * | 2000-01-24 | 2003-09-23 | Ucb Chip Inc. | Environmentally safe paint stripper emulsion |
| US7238653B2 (en) * | 2003-03-10 | 2007-07-03 | Hynix Semiconductor Inc. | Cleaning solution for photoresist and method for forming pattern using the same |
| US6884563B2 (en) * | 2003-05-20 | 2005-04-26 | Eastman Kodak Company | Thermal imaging material containing combustible nitro-resin particles |
| US6986944B2 (en) * | 2003-05-20 | 2006-01-17 | Eastman Kodak Company | Core-shell nitro-resin particles and method of preparation |
| US20050166794A1 (en) * | 2004-02-04 | 2005-08-04 | Bauer Richard D. | Binder additive for inkjet ink |
| KR20070043696A (ko) * | 2004-03-02 | 2007-04-25 | 폴리 코트 피티와이 리미티드 | 도장형 하도제계 |
| WO2008011658A1 (en) * | 2006-07-26 | 2008-01-31 | Acquos Pty Ltd | Redispersible polymer powders |
| US20090163635A1 (en) * | 2007-12-19 | 2009-06-25 | Eastman Chemical Company | Aqueous dispersions of adhesion promoters |
| WO2010057092A1 (en) * | 2008-11-14 | 2010-05-20 | Peach State Labs, Inc. | Compositions for treating textiles and carpet and applications thereof |
| US9963626B2 (en) * | 2014-03-14 | 2018-05-08 | Rainforest Technologies, Llc | Anti-skid compositions and methods of making and using the same |
| US10658121B2 (en) * | 2017-10-18 | 2020-05-19 | Kemet Electronics Corporation | Process for forming a solid electrolytic capacitor |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2171765A (en) * | 1934-12-31 | 1939-09-05 | Rohm & Haas | Process for the polymerization of methyl methacrylate |
| US2839479A (en) * | 1954-02-23 | 1958-06-17 | Eastman Kodak Co | Polymeric composition of an acrylic acid ester and cellulose acetate and method of preparation |
| US3061598A (en) * | 1959-03-02 | 1962-10-30 | Sartomer Resins Inc | Method of polymerizing methacrylate ester monomer in the presence of a polymer and a cyclohexly amine |
| GB1316693A (en) * | 1969-05-23 | 1973-05-09 | Fuji Photo Film Co Ltd | Process for suspension polymerization |
-
1974
- 1974-07-02 US US05/485,271 patent/US3953386A/en not_active Expired - Lifetime
-
1975
- 1975-06-27 CA CA230,331A patent/CA1052487A/en not_active Expired
- 1975-06-30 JP JP50080165A patent/JPS5917123B2/ja not_active Expired
- 1975-06-30 CH CH848175A patent/CH601385A5/xx not_active IP Right Cessation
- 1975-06-30 NO NO752377A patent/NO147071C/no unknown
- 1975-06-30 GB GB27563/75A patent/GB1515723A/en not_active Expired
- 1975-07-01 NL NLAANVRAGE7507829,A patent/NL183191C/xx not_active IP Right Cessation
- 1975-07-01 SE SE7507542A patent/SE416209B/xx not_active IP Right Cessation
- 1975-07-01 ZA ZA00754214A patent/ZA754214B/xx unknown
- 1975-07-01 FR FR7520608A patent/FR2277101A1/fr active Granted
- 1975-07-01 FI FI751929A patent/FI58926C/fi not_active IP Right Cessation
- 1975-07-01 IT IT25012/75A patent/IT1039618B/it active
- 1975-07-01 BE BE157874A patent/BE830871A/xx not_active IP Right Cessation
- 1975-07-01 BR BR5289/75D patent/BR7504131A/pt unknown
- 1975-07-02 DE DE2529547A patent/DE2529547C2/de not_active Expired
- 1975-07-02 PH PH17337A patent/PH12452A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BR7504131A (pt) | 1976-06-29 |
| FI58926B (fi) | 1981-01-30 |
| US3953386A (en) | 1976-04-27 |
| CH601385A5 (xx) | 1978-07-14 |
| PH12452A (en) | 1979-03-08 |
| NL183191C (nl) | 1988-08-16 |
| NO147071C (no) | 1983-01-26 |
| FR2277101A1 (fr) | 1976-01-30 |
| DE2529547C2 (de) | 1989-06-29 |
| DE2529547A1 (de) | 1976-01-22 |
| FI751929A (xx) | 1976-01-03 |
| GB1515723A (en) | 1978-06-28 |
| JPS5917123B2 (ja) | 1984-04-19 |
| JPS5128188A (xx) | 1976-03-09 |
| ZA754214B (en) | 1976-06-30 |
| SE416209B (sv) | 1980-12-08 |
| FR2277101B1 (xx) | 1980-04-30 |
| CA1052487A (en) | 1979-04-10 |
| NL7507829A (nl) | 1976-01-06 |
| NO752377L (xx) | 1976-01-05 |
| NO147071B (no) | 1982-10-18 |
| IT1039618B (it) | 1979-12-10 |
| AU8246675A (en) | 1977-01-06 |
| SE7507542L (sv) | 1976-01-05 |
| BE830871A (fr) | 1976-01-02 |
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Owner name: E.I. DU PONT DE NEMOURS AND COMPANY |