FI68248C - Saett vid polymerisation av eteniskt omaettade monomerer. - Google Patents
Saett vid polymerisation av eteniskt omaettade monomerer. Download PDFInfo
- Publication number
- FI68248C FI68248C FI810214A FI810214A FI68248C FI 68248 C FI68248 C FI 68248C FI 810214 A FI810214 A FI 810214A FI 810214 A FI810214 A FI 810214A FI 68248 C FI68248 C FI 68248C
- Authority
- FI
- Finland
- Prior art keywords
- ethoxylated
- vinyl chloride
- dispersion
- polymerization
- initiator
- Prior art date
Links
- 238000006116 polymerization reaction Methods 0.000 title claims description 24
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 title claims description 20
- 238000000034 method Methods 0.000 title claims description 13
- 239000000178 monomer Substances 0.000 title claims description 10
- 239000006185 dispersion Substances 0.000 claims description 61
- 239000003999 initiator Substances 0.000 claims description 37
- 239000007787 solid Substances 0.000 claims description 17
- 239000000194 fatty acid Substances 0.000 claims description 13
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 12
- 229930195729 fatty acid Natural products 0.000 claims description 12
- 150000004665 fatty acids Chemical class 0.000 claims description 9
- -1 peroxide carbonate Chemical class 0.000 claims description 9
- 150000001451 organic peroxides Chemical class 0.000 claims description 8
- 239000012875 nonionic emulsifier Substances 0.000 claims description 7
- 150000002191 fatty alcohols Chemical class 0.000 claims description 6
- 239000002562 thickening agent Substances 0.000 claims description 3
- 239000003995 emulsifying agent Substances 0.000 description 48
- 229920000642 polymer Polymers 0.000 description 15
- 150000002978 peroxides Chemical class 0.000 description 10
- 238000003860 storage Methods 0.000 description 10
- 239000000126 substance Substances 0.000 description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 7
- 239000000084 colloidal system Substances 0.000 description 7
- BEQKKZICTDFVMG-UHFFFAOYSA-N 1,2,3,4,6-pentaoxepane-5,7-dione Chemical compound O=C1OOOOC(=O)O1 BEQKKZICTDFVMG-UHFFFAOYSA-N 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 230000001681 protective effect Effects 0.000 description 6
- 125000004122 cyclic group Chemical group 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 5
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 5
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 5
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 5
- 150000003254 radicals Chemical class 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 230000000379 polymerizing effect Effects 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- 239000004372 Polyvinyl alcohol Substances 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000010292 electrical insulation Methods 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 238000007689 inspection Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- 238000005191 phase separation Methods 0.000 description 3
- 229920005862 polyol Polymers 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- 150000005846 sugar alcohols Polymers 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 2
- LGJCFVYMIJLQJO-UHFFFAOYSA-N 1-dodecylperoxydodecane Chemical compound CCCCCCCCCCCCOOCCCCCCCCCCCC LGJCFVYMIJLQJO-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 239000012933 diacyl peroxide Substances 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229920000847 nonoxynol Polymers 0.000 description 2
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 150000003077 polyols Chemical class 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- KFUSEUYYWQURPO-UHFFFAOYSA-N 1,2-dichloroethene Chemical compound ClC=CCl KFUSEUYYWQURPO-UHFFFAOYSA-N 0.000 description 1
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical compound CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- 229920000896 Ethulose Polymers 0.000 description 1
- 239000001859 Ethyl hydroxyethyl cellulose Substances 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 229920001213 Polysorbate 20 Polymers 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 235000019326 ethyl hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000001761 ethyl methyl cellulose Substances 0.000 description 1
- 235000010944 ethyl methyl cellulose Nutrition 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- OCWMFVJKFWXKNZ-UHFFFAOYSA-L lead(2+);oxygen(2-);sulfate Chemical compound [O-2].[O-2].[O-2].[Pb+2].[Pb+2].[Pb+2].[Pb+2].[O-]S([O-])(=O)=O OCWMFVJKFWXKNZ-UHFFFAOYSA-L 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 125000005641 methacryl group Chemical group 0.000 description 1
- WFUPNMGWVAEEFM-UHFFFAOYSA-N methoxycarbonyloxy methyl carbonate Chemical compound COC(=O)OOC(=O)OC WFUPNMGWVAEEFM-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical class CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 1
- 150000002888 oleic acid derivatives Chemical class 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 150000002976 peresters Chemical class 0.000 description 1
- 125000005634 peroxydicarbonate group Chemical group 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
- 229960002675 xylitol Drugs 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
- H01B3/44—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes vinyl resins; acrylic resins
- H01B3/443—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes vinyl resins; acrylic resins from vinylhalogenides or other halogenoethylenic compounds
-
- 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
-
- 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
- C08F2/38—Polymerisation using regulators, e.g. chain terminating agents, e.g. telomerisation
- C08F2/40—Polymerisation using regulators, e.g. chain terminating agents, e.g. telomerisation using retarding agents
-
- 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
- C08F4/00—Polymerisation catalysts
- C08F4/28—Oxygen or compounds releasing free oxygen
- C08F4/32—Organic compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- Polymerisation Methods In General (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymerization Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE8000669 | 1980-01-28 | ||
| SE8000669A SE435844C (sv) | 1980-01-28 | 1980-01-28 | Saett vid polymerisation av vinylklorid och vattendispersion foer anvaendning vid polymerisation av vinylklorid |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI810214L FI810214L (fi) | 1981-07-29 |
| FI68248B FI68248B (fi) | 1985-04-30 |
| FI68248C true FI68248C (fi) | 1990-05-15 |
Family
ID=20340098
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI810214A FI68248C (fi) | 1980-01-28 | 1981-01-26 | Saett vid polymerisation av eteniskt omaettade monomerer. |
Country Status (14)
| Country | Link |
|---|---|
| US (2) | US4499250A (enExample) |
| JP (1) | JPS5851002B2 (enExample) |
| BE (1) | BE887249A (enExample) |
| CA (1) | CA1160618A (enExample) |
| CH (1) | CH644135A5 (enExample) |
| DE (1) | DE3102781A1 (enExample) |
| ES (1) | ES8201177A1 (enExample) |
| FI (1) | FI68248C (enExample) |
| FR (1) | FR2474509B1 (enExample) |
| GB (1) | GB2068008B (enExample) |
| IT (1) | IT1170650B (enExample) |
| NL (1) | NL187534C (enExample) |
| NO (1) | NO158808C (enExample) |
| SE (1) | SE435844C (enExample) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5162280A (en) * | 1988-01-27 | 1992-11-10 | Witco Corporation | Aqueous dispersions of aromatic diacyl peroxides |
| US5057479A (en) * | 1990-05-09 | 1991-10-15 | Witco Corporation | Aqueous dispersions of aromatic diacyl peroxides |
| DE69023526T3 (de) * | 1989-03-23 | 2002-12-05 | Orica Australia Pty Ltd., Melbourne | Additionspolymerteilchen. |
| US5300600A (en) * | 1989-10-12 | 1994-04-05 | Witco Corporation | Aqueous dispersions of peroxides |
| DE19537936A1 (de) * | 1995-10-12 | 1997-04-17 | Basf Ag | Verfahren zur Herstellung von koagulatfreien Polymerdispersionen |
| KR100501969B1 (ko) * | 1996-10-30 | 2005-07-20 | 아크조 노벨 엔.브이. | 폴리비닐알콜 및 계면활성제로 구성된 개시제 조성물의 제조방법 |
| TW426707B (en) | 1997-07-24 | 2001-03-21 | Akzo Nobel Nv | Emulsions of peroxyesters |
| JP4271141B2 (ja) * | 2002-05-08 | 2009-06-03 | アクゾ ノーベル ナムローゼ フェンノートシャップ | 低い化学的酸素要求量値を有する非常に濃厚で安定かつ安全なジアシルパーオキシドおよびパーオキシジカーボネートエマルジョン |
| FR2995905B1 (fr) | 2012-09-21 | 2015-10-16 | Arkema France | Composition de peroxyde organique sans agent colloide |
| US20220064371A1 (en) * | 2020-09-03 | 2022-03-03 | Jain-Chem, Ltd. | Non-sulfonated polyester acrylates and coatings employing same |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4938988A (enExample) * | 1972-08-17 | 1974-04-11 | ||
| US3825509A (en) * | 1972-11-13 | 1974-07-23 | Goodrich Co B F | Initiator emulsion for olefinic polymerization reactions |
| AR208425A1 (es) * | 1975-03-14 | 1976-12-27 | Akzo Nv | Procedimiento para la preparacion de una suspension acuosa conteniendo un peroxido organico solido a una temperatura de aproximadamente 20 c |
| US4092470A (en) * | 1975-03-14 | 1978-05-30 | Akzona Incorporated | Stable, pumpable, aqueous suspensions of organic peroxides |
| US3988261A (en) * | 1975-07-28 | 1976-10-26 | Ppg Industries, Inc. | Frozen organic peroxide emulsion |
| DE2629467A1 (de) * | 1976-06-30 | 1978-01-05 | Wacker Chemie Gmbh | Waessrige katalysatorkonfektion |
| JPS5343787A (en) * | 1976-10-01 | 1978-04-20 | Kao Corp | Emulsifier for emulsion polymerization |
| SE435843B (sv) * | 1980-01-28 | 1984-10-22 | Kenogard Ab | Sett vid polymerisation av vinylklorid och vattendispersion for anvendning vid polymerisation av vinylklorid |
| DE3205146A1 (de) * | 1982-02-13 | 1983-08-18 | Azo-Maschinenfabrik Adolf Zimmermann Gmbh, 6960 Osterburken | Vorrichtung zum versorgen stationaerer heizungsanlagen mit schuettfaehigen brennstoffen |
-
1980
- 1980-01-28 SE SE8000669A patent/SE435844C/sv not_active IP Right Cessation
-
1981
- 1981-01-26 IT IT47635/81A patent/IT1170650B/it active
- 1981-01-26 FI FI810214A patent/FI68248C/fi not_active IP Right Cessation
- 1981-01-26 FR FR8101351A patent/FR2474509B1/fr not_active Expired
- 1981-01-26 JP JP56009142A patent/JPS5851002B2/ja not_active Expired
- 1981-01-27 CH CH52481A patent/CH644135A5/de not_active IP Right Cessation
- 1981-01-27 NO NO810273A patent/NO158808C/no not_active IP Right Cessation
- 1981-01-27 ES ES498833A patent/ES8201177A1/es not_active Expired
- 1981-01-27 NL NLAANVRAGE8100378,A patent/NL187534C/xx not_active IP Right Cessation
- 1981-01-27 CA CA000369384A patent/CA1160618A/en not_active Expired
- 1981-01-27 BE BE0/203613A patent/BE887249A/fr not_active IP Right Cessation
- 1981-01-28 DE DE19813102781 patent/DE3102781A1/de active Granted
- 1981-01-28 GB GB8102601A patent/GB2068008B/en not_active Expired
-
1982
- 1982-07-27 US US06/402,276 patent/US4499250A/en not_active Expired - Lifetime
-
1984
- 1984-07-17 US US06/631,785 patent/US4547481A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| IT8147635A0 (it) | 1981-01-26 |
| SE8000669L (sv) | 1981-07-29 |
| CA1160618A (en) | 1984-01-17 |
| BE887249A (fr) | 1981-07-27 |
| FR2474509A1 (fr) | 1981-07-31 |
| ES498833A0 (es) | 1981-12-01 |
| SE435844B (sv) | 1984-10-22 |
| JPS56110703A (en) | 1981-09-02 |
| GB2068008B (en) | 1984-02-08 |
| FI810214L (fi) | 1981-07-29 |
| NO158808B (no) | 1988-07-25 |
| DE3102781A1 (de) | 1982-02-04 |
| NL8100378A (nl) | 1981-08-17 |
| DE3102781C2 (enExample) | 1987-05-21 |
| NO810273L (no) | 1981-07-29 |
| ES8201177A1 (es) | 1981-12-01 |
| NL187534C (nl) | 1993-11-16 |
| SE435844C (sv) | 1989-04-17 |
| FI68248B (fi) | 1985-04-30 |
| NO158808C (no) | 1988-11-02 |
| CH644135A5 (de) | 1984-07-13 |
| US4547481A (en) | 1985-10-15 |
| IT1170650B (it) | 1987-06-03 |
| FR2474509B1 (fr) | 1985-11-22 |
| JPS5851002B2 (ja) | 1983-11-14 |
| US4499250A (en) | 1985-02-12 |
| GB2068008A (en) | 1981-08-05 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MA | Patent expired |
Owner name: BEROL NOBEL AB |