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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- 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)
Claims (9)
1. Vattenhaltig polymeremulsion användbar som skydds- och dekorations-— beläggning samt som lim, kännetecknad därav, att den omfattar en kontinuerlig vattenfas, som innehaller 0,1-10 %, beräknat pä den slutliga poly-merens totala vikt, av ett ytaktivt medel, i vilken vattenfas dispergerats partiklar med en medeldiameter av upp till 5 pn, varvid partiklarna väsentligen utgörs av en homogen blandning, som bildats av 20-60 viktdelar, beräknat pä hela polymeren, cellulosaester, som är olöslig i vatten, och U0-80 viktdelar, beräknat pä hela polymeren, av en polymer, som är härledd ur ätminstone en monomer med formeIn R .0 f # CH =C-C xo^1 väri R är väte eller en metylradikal och R^är en alkylradikal med 1-20 kolatomer, varvid cellulosaestern är löslig i monomeren i en mängd av minst 10 vikt-#.
2. Emulsion enligt patentkravet 1, kännetecknad därav, att monomeren är metylmetakrylat, 2-etylhexylakrylat eller n-butylmetakrylat.
3· Emulsion enligt patentkravet 1 eller 2,kännetecknad därav, att cellulosaestern är nitrocellulose. Förfarande för framställning av en vattenhaltig polymeremulsion enligt nägot av föregäende krav, kännetecknat därav, att man med varandra blandar vatten, ytaktivt medel och minst en cellulosaester, företrädesvis nitro-cellulosa, samt minst en monomer med formeln R 0 f S CH2=C-C "Nj-R väri R är väte eller en metylradikal och R^ är en alkylradikal med 1-20 kolatomer, varvid cellulosaestern löser sig i monomeren och bildar under betingelser, vid vilka används skärkraft, en cellulosaester-monomerpartikeldispersion, i vilken partiklarna har en medeldiameter av upp tili 5 pn, och underkastar dispersionen sädana betingelser, vid vilka monomeren i partiklarna polymeriseras genom fri-radikalpolymerisation under bildande av en väsentligen homogen blandning av minst tvä polymerer i emulsionens partiklar, varvid cellulosaester-monomerkoncentrations- förhallandet är 20-60 viktdelar cellulosaester och UO-ÖO viktdelar monomer.
5. Förfarande enligt patentkravet , kännetecknat därav, att partiklarna har en diameter av upp till 1 mikrometer i genomsnitt.
6. Förfarande enligt patentkravet kännetecknat därav, att monomeren är metylmetakrylat, 2-etylhexylakrylat eller n-butylmetakrylat.
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 (sv) | 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 (sv) |
| JP (1) | JPS5917123B2 (sv) |
| BE (1) | BE830871A (sv) |
| BR (1) | BR7504131A (sv) |
| CA (1) | CA1052487A (sv) |
| CH (1) | CH601385A5 (sv) |
| DE (1) | DE2529547C2 (sv) |
| FI (1) | FI58926C (sv) |
| FR (1) | FR2277101A1 (sv) |
| GB (1) | GB1515723A (sv) |
| IT (1) | IT1039618B (sv) |
| NL (1) | NL183191C (sv) |
| NO (1) | NO147071C (sv) |
| PH (1) | PH12452A (sv) |
| SE (1) | SE416209B (sv) |
| ZA (1) | ZA754214B (sv) |
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/sv 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 (sv) | 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 (sv) | 1976-01-03 |
| GB1515723A (en) | 1978-06-28 |
| JPS5917123B2 (ja) | 1984-04-19 |
| JPS5128188A (sv) | 1976-03-09 |
| ZA754214B (en) | 1976-06-30 |
| SE416209B (sv) | 1980-12-08 |
| FR2277101B1 (sv) | 1980-04-30 |
| CA1052487A (en) | 1979-04-10 |
| NL7507829A (nl) | 1976-01-06 |
| NO752377L (sv) | 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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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM | Patent lapsed |
Owner name: E.I. DU PONT DE NEMOURS AND COMPANY |