FI73228C - Foerfarande foer framstaellning av en steriskt stabiliserad vattenhaltig polymerdispersion. - Google Patents
Foerfarande foer framstaellning av en steriskt stabiliserad vattenhaltig polymerdispersion. Download PDFInfo
- Publication number
- FI73228C FI73228C FI832733A FI832733A FI73228C FI 73228 C FI73228 C FI 73228C FI 832733 A FI832733 A FI 832733A FI 832733 A FI832733 A FI 832733A FI 73228 C FI73228 C FI 73228C
- Authority
- FI
- Finland
- Prior art keywords
- monomer
- water
- component
- soluble
- surfactant
- Prior art date
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- 239000004815 dispersion polymer Substances 0.000 title claims abstract description 6
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- 239000000178 monomer Substances 0.000 claims abstract description 94
- 239000004094 surface-active agent Substances 0.000 claims abstract description 39
- 229920000642 polymer Polymers 0.000 claims abstract description 37
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 34
- 239000003999 initiator Substances 0.000 claims abstract description 26
- 239000008346 aqueous phase Substances 0.000 claims abstract description 18
- 239000012071 phase Substances 0.000 claims abstract description 13
- 239000000203 mixture Substances 0.000 claims abstract description 11
- 238000000034 method Methods 0.000 claims description 37
- 150000001875 compounds Chemical class 0.000 claims description 32
- 238000006116 polymerization reaction Methods 0.000 claims description 29
- 230000008569 process Effects 0.000 claims description 27
- -1 polyoxyethylene Polymers 0.000 claims description 18
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 11
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 10
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 9
- 238000002360 preparation method Methods 0.000 claims description 8
- 229920001400 block copolymer Polymers 0.000 claims description 6
- 239000004615 ingredient Substances 0.000 claims description 6
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 5
- 239000002202 Polyethylene glycol Substances 0.000 claims description 5
- 238000009833 condensation Methods 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 229920001223 polyethylene glycol Polymers 0.000 claims description 5
- NICLKHGIKDZZGV-UHFFFAOYSA-N 2-cyanopentanoic acid Chemical compound CCCC(C#N)C(O)=O NICLKHGIKDZZGV-UHFFFAOYSA-N 0.000 claims description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims description 4
- 239000007869 azo polymerization initiator Substances 0.000 claims description 4
- 230000005494 condensation Effects 0.000 claims description 4
- 150000003254 radicals Chemical class 0.000 claims description 4
- 239000003995 emulsifying agent Substances 0.000 claims description 3
- 239000002736 nonionic surfactant Substances 0.000 claims description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 2
- 239000005977 Ethylene Substances 0.000 claims description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims 2
- 230000000903 blocking effect Effects 0.000 claims 1
- 239000003086 colorant Substances 0.000 claims 1
- 210000005036 nerve Anatomy 0.000 claims 1
- 229910052759 nickel Inorganic materials 0.000 claims 1
- 238000000638 solvent extraction Methods 0.000 claims 1
- 239000008199 coating composition Substances 0.000 abstract description 2
- 238000009472 formulation Methods 0.000 abstract 1
- 239000002243 precursor Substances 0.000 description 20
- 239000002245 particle Substances 0.000 description 17
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- 150000002148 esters Chemical class 0.000 description 11
- 229920000126 latex Polymers 0.000 description 10
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 9
- 239000004816 latex Substances 0.000 description 9
- 239000003381 stabilizer Substances 0.000 description 9
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 8
- 239000008367 deionised water Substances 0.000 description 8
- 229910021641 deionized water Inorganic materials 0.000 description 8
- 230000002209 hydrophobic effect Effects 0.000 description 8
- 239000012736 aqueous medium Substances 0.000 description 7
- 238000009826 distribution Methods 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
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- 238000003556 assay Methods 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 238000004945 emulsification Methods 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 230000006641 stabilisation Effects 0.000 description 4
- 238000011105 stabilization Methods 0.000 description 4
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 238000003482 Pinner synthesis reaction Methods 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 3
- 230000004888 barrier function Effects 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 239000012986 chain transfer agent Substances 0.000 description 3
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 3
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 3
- 238000011065 in-situ storage Methods 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 239000003505 polymerization initiator Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- VBZBISQOWJYWCC-UHFFFAOYSA-N 2-(2-carboxypropan-2-yldiazenyl)-2-methylpropanoic acid Chemical compound OC(=O)C(C)(C)N=NC(C)(C)C(O)=O VBZBISQOWJYWCC-UHFFFAOYSA-N 0.000 description 2
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical class CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 2
- IJOUWMMZJISKHY-UHFFFAOYSA-N 2-hydroxypropan-2-yl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)(C)O IJOUWMMZJISKHY-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 2
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000007720 emulsion polymerization reaction Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 229920000578 graft copolymer Polymers 0.000 description 2
- 150000002430 hydrocarbons Chemical group 0.000 description 2
- VHRYZQNGTZXDNX-UHFFFAOYSA-N methacryloyl chloride Chemical compound CC(=C)C(Cl)=O VHRYZQNGTZXDNX-UHFFFAOYSA-N 0.000 description 2
- ODUCDPQEXGNKDN-UHFFFAOYSA-N nitroxyl Chemical compound O=N ODUCDPQEXGNKDN-UHFFFAOYSA-N 0.000 description 2
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- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000000047 product Substances 0.000 description 2
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- 230000000087 stabilizing effect Effects 0.000 description 2
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical group OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 2
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 229920003176 water-insoluble polymer Polymers 0.000 description 2
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 1
- WMRPYWCZRVZFIX-UHFFFAOYSA-N 1,2-dihydroxypropyl 2-[[1-(1,2-dihydroxypropoxy)-2-methyl-1-oxopropan-2-yl]diazenyl]-2-methylpropanoate Chemical compound OC(C(C)O)OC(C(C)(C)N=NC(C(=O)OC(C(C)O)O)(C)C)=O WMRPYWCZRVZFIX-UHFFFAOYSA-N 0.000 description 1
- VOBUAPTXJKMNCT-UHFFFAOYSA-N 1-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound CCCCCC(OC(=O)C=C)OC(=O)C=C VOBUAPTXJKMNCT-UHFFFAOYSA-N 0.000 description 1
- FRPZMMHWLSIFAZ-UHFFFAOYSA-N 10-undecenoic acid Chemical compound OC(=O)CCCCCCCCC=C FRPZMMHWLSIFAZ-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- 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 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
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- CTHJQRHPNQEPAB-UHFFFAOYSA-N 2-methoxyethenylbenzene Chemical compound COC=CC1=CC=CC=C1 CTHJQRHPNQEPAB-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- GDWQNWXRAPFIKB-UHFFFAOYSA-N 3-methoxypropyl 2-methylprop-2-enoate Chemical compound COCCCOC(=O)C(C)=C GDWQNWXRAPFIKB-UHFFFAOYSA-N 0.000 description 1
- HMHYBQHINBJJGL-UHFFFAOYSA-N 4-[(4-carboxy-4-cyanobutan-2-yl)diazenyl]-2-cyanopentanoic acid Chemical compound N#CC(C(O)=O)CC(C)N=NC(C)CC(C#N)C(O)=O HMHYBQHINBJJGL-UHFFFAOYSA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
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- 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 1
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- 150000003863 ammonium salts Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- AOJOEFVRHOZDFN-UHFFFAOYSA-N benzyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC1=CC=CC=C1 AOJOEFVRHOZDFN-UHFFFAOYSA-N 0.000 description 1
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- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
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- YHAIUSTWZPMYGG-UHFFFAOYSA-L disodium;2,2-dioctyl-3-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCCCCCC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CCCCCCCC YHAIUSTWZPMYGG-UHFFFAOYSA-L 0.000 description 1
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- FTQWRYSLUYAIRQ-UHFFFAOYSA-N n-[(octadecanoylamino)methyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCNC(=O)CCCCCCCCCCCCCCCCC FTQWRYSLUYAIRQ-UHFFFAOYSA-N 0.000 description 1
- QYZFTMMPKCOTAN-UHFFFAOYSA-N n-[2-(2-hydroxyethylamino)ethyl]-2-[[1-[2-(2-hydroxyethylamino)ethylamino]-2-methyl-1-oxopropan-2-yl]diazenyl]-2-methylpropanamide Chemical compound OCCNCCNC(=O)C(C)(C)N=NC(C)(C)C(=O)NCCNCCO QYZFTMMPKCOTAN-UHFFFAOYSA-N 0.000 description 1
- OSDZHDOKXGSWOD-UHFFFAOYSA-N nitroxyl;hydrochloride Chemical compound Cl.O=N OSDZHDOKXGSWOD-UHFFFAOYSA-N 0.000 description 1
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- 238000011017 operating method Methods 0.000 description 1
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
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- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 238000009210 therapy by ultrasound Methods 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 229960002703 undecylenic acid Drugs 0.000 description 1
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25B—REFRIGERATION MACHINES, PLANTS OR SYSTEMS; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS
- F25B15/00—Sorption machines, plants or systems, operating continuously, e.g. absorption type
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- General Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Mechanical Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Polymerisation Methods In General (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
- Paints Or Removers (AREA)
- High-Pressure Fuel Injection Pump Control (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Dental Preparations (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8221894 | 1982-07-29 | ||
| GB8221894 | 1982-07-29 |
Publications (4)
| Publication Number | Publication Date |
|---|---|
| FI832733A0 FI832733A0 (fi) | 1983-07-28 |
| FI832733A7 FI832733A7 (fi) | 1984-01-30 |
| FI73228B FI73228B (fi) | 1987-05-29 |
| FI73228C true FI73228C (fi) | 1987-09-10 |
Family
ID=10531977
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI832733A FI73228C (fi) | 1982-07-29 | 1983-07-28 | Foerfarande foer framstaellning av en steriskt stabiliserad vattenhaltig polymerdispersion. |
Country Status (18)
| Country | Link |
|---|---|
| EP (1) | EP0102707B1 (enExample) |
| JP (1) | JPS5942035A (enExample) |
| KR (1) | KR850001234A (enExample) |
| AT (1) | ATE22300T1 (enExample) |
| AU (1) | AU563538B2 (enExample) |
| BR (1) | BR8304018A (enExample) |
| CA (1) | CA1203339A (enExample) |
| DE (1) | DE3366274D1 (enExample) |
| DK (1) | DK343583A (enExample) |
| ES (1) | ES8502449A1 (enExample) |
| FI (1) | FI73228C (enExample) |
| GB (1) | GB2124636B (enExample) |
| IE (1) | IE55628B1 (enExample) |
| IN (1) | IN159166B (enExample) |
| NO (1) | NO832673L (enExample) |
| NZ (1) | NZ204862A (enExample) |
| PT (1) | PT77126B (enExample) |
| ZA (1) | ZA835222B (enExample) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3882173D1 (de) * | 1987-06-04 | 1993-08-12 | Ciba Geigy Ag | Lichtstabilisierte, epoxygruppenhaltige polymermikropartikel. |
| US5296627A (en) * | 1988-06-20 | 1994-03-22 | Ppg Industries, Inc. | Ethylenically unsaturated poly(alkyleneoxy) surfactants |
| KR920003118B1 (ko) * | 1988-06-20 | 1992-04-20 | 피피지 인더스트리즈, 인코포레이티드 | 중합가능한 계면활성제 |
| DE3902536A1 (de) * | 1989-01-28 | 1990-08-16 | Akzo Gmbh | Sterisch stabilisierte waessrige polymer-dispersionen |
| DE19709630C1 (de) * | 1997-03-08 | 1998-08-20 | Henkel Kgaa | Verfahren zur Herstellung von Polymeren |
| US6077921A (en) * | 1998-12-07 | 2000-06-20 | Ppg Industries Ohio, Inc. | Polymerizable polyol (allyl carbonate) compositions |
| WO2002022692A1 (fr) | 2000-09-11 | 2002-03-21 | Kao Corporation | Agent de surface destine a la polymerisation d'une emulsion |
| JP6656286B2 (ja) | 2018-03-29 | 2020-03-04 | 本田技研工業株式会社 | クランク角検出装置 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1379335A (en) * | 1973-08-14 | 1975-01-02 | Kendall & Co | Nonionic monomeric emulsion stabilizers |
| JPS5912681B2 (ja) * | 1973-12-29 | 1984-03-24 | 三洋化成工業株式会社 | 水性重合用乳化剤 |
| JPS5426851Y2 (enExample) * | 1974-01-12 | 1979-09-04 | ||
| NL160278C (nl) * | 1975-09-25 | 1979-10-15 | Synres Internationaal Nv | Werkwijze voor het bereiden van waterige emulsies van additiepolymeren. |
| CA1098248A (en) * | 1976-03-10 | 1981-03-24 | Richard G. Sinclair | Block copolymer dispersion stabilizer and aqueous dispersion polymerization therewith |
| DE2964171D1 (en) * | 1978-12-07 | 1983-01-05 | Ici Plc | Manufacture of polymer dispersions and coating compositions derived from them |
| GB2064562B (en) * | 1979-12-06 | 1983-04-07 | Ici Ltd | Production of non-aqueous polymer microparticle dispersions |
| JPS5846243B2 (ja) * | 1980-09-19 | 1983-10-15 | 積水化学工業株式会社 | 血清学的診断試薬用ラテツクスの製造方法 |
| DE3269599D1 (en) * | 1981-06-29 | 1986-04-10 | Dulux Australia Ltd | Stable aqueous film-forming dispersions |
| GB2120261B (en) * | 1982-05-20 | 1985-10-30 | Ici Plc | Polymerisation process |
-
1983
- 1983-07-05 GB GB08318137A patent/GB2124636B/en not_active Expired
- 1983-07-06 EP EP83303943A patent/EP0102707B1/en not_active Expired
- 1983-07-06 AT AT83303943T patent/ATE22300T1/de not_active IP Right Cessation
- 1983-07-06 DE DE8383303943T patent/DE3366274D1/de not_active Expired
- 1983-07-11 NZ NZ204862A patent/NZ204862A/en unknown
- 1983-07-11 IN IN471/DEL/83A patent/IN159166B/en unknown
- 1983-07-11 IE IE1615/83A patent/IE55628B1/en unknown
- 1983-07-15 AU AU16870/83A patent/AU563538B2/en not_active Ceased
- 1983-07-18 ZA ZA835222A patent/ZA835222B/xx unknown
- 1983-07-22 NO NO832673A patent/NO832673L/no unknown
- 1983-07-27 BR BR8304018A patent/BR8304018A/pt not_active IP Right Cessation
- 1983-07-27 DK DK343583A patent/DK343583A/da not_active Application Discontinuation
- 1983-07-28 FI FI832733A patent/FI73228C/fi not_active IP Right Cessation
- 1983-07-28 PT PT77126A patent/PT77126B/pt unknown
- 1983-07-29 CA CA000433649A patent/CA1203339A/en not_active Expired
- 1983-07-29 JP JP58137884A patent/JPS5942035A/ja active Granted
- 1983-07-29 KR KR1019830003547A patent/KR850001234A/ko not_active Withdrawn
- 1983-07-29 ES ES524564A patent/ES8502449A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| PT77126A (en) | 1983-08-01 |
| JPH057403B2 (enExample) | 1993-01-28 |
| KR850001234A (ko) | 1985-03-16 |
| CA1203339A (en) | 1986-04-15 |
| AU563538B2 (en) | 1987-07-16 |
| FI832733A0 (fi) | 1983-07-28 |
| NO832673L (no) | 1984-01-30 |
| EP0102707B1 (en) | 1986-09-17 |
| IE831615L (en) | 1984-01-29 |
| BR8304018A (pt) | 1984-05-29 |
| FI73228B (fi) | 1987-05-29 |
| IE55628B1 (en) | 1990-12-05 |
| GB2124636A (en) | 1984-02-22 |
| ES524564A0 (es) | 1985-01-01 |
| ZA835222B (en) | 1984-12-24 |
| ATE22300T1 (de) | 1986-10-15 |
| IN159166B (enExample) | 1987-04-04 |
| JPS5942035A (ja) | 1984-03-08 |
| NZ204862A (en) | 1986-01-24 |
| DK343583D0 (da) | 1983-07-27 |
| GB8318137D0 (en) | 1983-08-03 |
| ES8502449A1 (es) | 1985-01-01 |
| AU1687083A (en) | 1984-02-02 |
| DE3366274D1 (en) | 1986-10-23 |
| EP0102707A1 (en) | 1984-03-14 |
| DK343583A (da) | 1984-01-30 |
| FI832733A7 (fi) | 1984-01-30 |
| PT77126B (en) | 1986-07-15 |
| GB2124636B (en) | 1985-08-07 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM | Patent lapsed |
Owner name: IMPERIAL CHEMICAL INDUSTRIES PLC Owner name: DULUX AUSTRALIA LIMITED |