SK284473B6 - Vodná emulzia peroxyesteru a jej použitie - Google Patents
Vodná emulzia peroxyesteru a jej použitie Download PDFInfo
- Publication number
- SK284473B6 SK284473B6 SK96-2000A SK962000A SK284473B6 SK 284473 B6 SK284473 B6 SK 284473B6 SK 962000 A SK962000 A SK 962000A SK 284473 B6 SK284473 B6 SK 284473B6
- Authority
- SK
- Slovakia
- Prior art keywords
- peroxyester
- emulsions
- aqueous emulsion
- emulsion according
- weight
- Prior art date
Links
- 239000000839 emulsion Substances 0.000 title claims abstract description 108
- 229920002689 polyvinyl acetate Polymers 0.000 claims abstract description 44
- 239000011118 polyvinyl acetate Substances 0.000 claims abstract description 36
- 230000007062 hydrolysis Effects 0.000 claims abstract description 22
- 238000006460 hydrolysis reaction Methods 0.000 claims abstract description 22
- 239000007798 antifreeze agent Substances 0.000 claims abstract description 19
- 150000002191 fatty alcohols Chemical class 0.000 claims abstract description 10
- 239000002736 nonionic surfactant Substances 0.000 claims abstract description 10
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 8
- 239000000194 fatty acid Substances 0.000 claims abstract description 8
- 229930195729 fatty acid Natural products 0.000 claims abstract description 8
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 7
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 5
- 229920001400 block copolymer Polymers 0.000 claims abstract description 5
- 239000004094 surface-active agent Substances 0.000 claims description 34
- 239000000084 colloidal system Substances 0.000 claims description 21
- 230000001681 protective effect Effects 0.000 claims description 19
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 15
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 14
- 238000006116 polymerization reaction Methods 0.000 claims description 12
- 239000000126 substance Substances 0.000 claims description 11
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 5
- 229920000642 polymer Polymers 0.000 claims description 5
- -1 prapanediol Chemical compound 0.000 claims description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 4
- 239000000178 monomer Substances 0.000 claims description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 2
- 241000694440 Colpidium aqueous Species 0.000 claims 1
- 239000013543 active substance Substances 0.000 claims 1
- 238000003860 storage Methods 0.000 abstract description 11
- 239000000203 mixture Substances 0.000 description 23
- 230000000052 comparative effect Effects 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 238000000034 method Methods 0.000 description 10
- 150000002978 peroxides Chemical class 0.000 description 10
- 238000004519 manufacturing process Methods 0.000 description 9
- 238000000354 decomposition reaction Methods 0.000 description 8
- 239000004800 polyvinyl chloride Substances 0.000 description 8
- 229920000915 polyvinyl chloride Polymers 0.000 description 7
- 238000009472 formulation Methods 0.000 description 6
- 239000011149 active material Substances 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 239000012071 phase Substances 0.000 description 5
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 239000003999 initiator Substances 0.000 description 4
- ZBJVLWIYKOAYQH-UHFFFAOYSA-N naphthalen-2-yl 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=C(C=CC=C2)C2=C1 ZBJVLWIYKOAYQH-UHFFFAOYSA-N 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 229920000847 nonoxynol Polymers 0.000 description 3
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 3
- 239000011368 organic material Substances 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- 238000010557 suspension polymerization reaction Methods 0.000 description 3
- 239000002562 thickening agent Substances 0.000 description 3
- QFMDFTQOJHFVNR-UHFFFAOYSA-N 1-[2,2-dichloro-1-(4-ethylphenyl)ethyl]-4-ethylbenzene Chemical compound C1=CC(CC)=CC=C1C(C(Cl)Cl)C1=CC=C(CC)C=C1 QFMDFTQOJHFVNR-UHFFFAOYSA-N 0.000 description 2
- RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 description 2
- NUIZZJWNNGJSGL-UHFFFAOYSA-N 2-phenylpropan-2-yl 2,2-dimethyloctaneperoxoate Chemical compound CCCCCCC(C)(C)C(=O)OOC(C)(C)c1ccccc1 NUIZZJWNNGJSGL-UHFFFAOYSA-N 0.000 description 2
- 241000251468 Actinopterygii Species 0.000 description 2
- 229920001213 Polysorbate 20 Polymers 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 235000010980 cellulose Nutrition 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000007720 emulsion polymerization reaction Methods 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000005191 phase separation Methods 0.000 description 2
- 239000008363 phosphate buffer Substances 0.000 description 2
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 2
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- NMOALOSNPWTWRH-UHFFFAOYSA-N tert-butyl 7,7-dimethyloctaneperoxoate Chemical compound CC(C)(C)CCCCCC(=O)OOC(C)(C)C NMOALOSNPWTWRH-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 239000000230 xanthan gum Substances 0.000 description 2
- 235000010493 xanthan gum Nutrition 0.000 description 2
- 229920001285 xanthan gum Polymers 0.000 description 2
- 229940082509 xanthan gum Drugs 0.000 description 2
- HGXJDMCMYLEZMJ-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy 2,2-dimethylpropaneperoxoate Chemical compound CC(C)(C)OOOC(=O)C(C)(C)C HGXJDMCMYLEZMJ-UHFFFAOYSA-N 0.000 description 1
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- BEQKKZICTDFVMG-UHFFFAOYSA-N 1,2,3,4,6-pentaoxepane-5,7-dione Chemical compound O=C1OOOOC(=O)O1 BEQKKZICTDFVMG-UHFFFAOYSA-N 0.000 description 1
- RAWISQFSQWIXCW-UHFFFAOYSA-N 2-methylbutan-2-yl 2,2-dimethyloctaneperoxoate Chemical compound CCCCCCC(C)(C)C(=O)OOC(C)(C)CC RAWISQFSQWIXCW-UHFFFAOYSA-N 0.000 description 1
- AQKYLAIZOGOPAW-UHFFFAOYSA-N 2-methylbutan-2-yl 2,2-dimethylpropaneperoxoate Chemical compound CCC(C)(C)OOC(=O)C(C)(C)C AQKYLAIZOGOPAW-UHFFFAOYSA-N 0.000 description 1
- IFXDUNDBQDXPQZ-UHFFFAOYSA-N 2-methylbutan-2-yl 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOC(C)(C)CC IFXDUNDBQDXPQZ-UHFFFAOYSA-N 0.000 description 1
- XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical class CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 description 1
- 241000220479 Acacia Species 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 235000010643 Leucaena leucocephala Nutrition 0.000 description 1
- 229920009204 Methacrylate-butadiene-styrene Polymers 0.000 description 1
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 229920004482 WACKER® Polymers 0.000 description 1
- JUIBLDFFVYKUAC-UHFFFAOYSA-N [5-(2-ethylhexanoylperoxy)-2,5-dimethylhexan-2-yl] 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOC(C)(C)CCC(C)(C)OOC(=O)C(CC)CCCC JUIBLDFFVYKUAC-UHFFFAOYSA-N 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 238000000149 argon plasma sintering Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- LKAVYBZHOYOUSX-UHFFFAOYSA-N buta-1,3-diene;2-methylprop-2-enoic acid;styrene Chemical compound C=CC=C.CC(=C)C(O)=O.C=CC1=CC=CC=C1 LKAVYBZHOYOUSX-UHFFFAOYSA-N 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 210000004534 cecum Anatomy 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical class CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000002372 labelling Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
- 239000003340 retarding agent Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- WYKYCHHWIJXDAO-UHFFFAOYSA-N tert-butyl 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOC(C)(C)C WYKYCHHWIJXDAO-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- KXXVYHRSWQEUBX-UHFFFAOYSA-N tert-butyl heptaneperoxoate Chemical compound CCCCCCC(=O)OOC(C)(C)C KXXVYHRSWQEUBX-UHFFFAOYSA-N 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C409/00—Peroxy 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
- C08F4/00—Polymerisation catalysts
- C08F4/28—Oxygen or compounds releasing free oxygen
- C08F4/32—Organic compounds
- C08F4/34—Per-compounds with one peroxy-radical
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polymerisation Methods In General (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Polymerization Catalysts (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Detergent Compositions (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP97202307 | 1997-07-24 | ||
| PCT/EP1998/004015 WO1999005101A1 (fr) | 1997-07-24 | 1998-06-16 | Emulsions de peroxyesters |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SK962000A3 SK962000A3 (en) | 2000-09-12 |
| SK284473B6 true SK284473B6 (sk) | 2005-04-01 |
Family
ID=8228586
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK96-2000A SK284473B6 (sk) | 1997-07-24 | 1998-06-16 | Vodná emulzia peroxyesteru a jej použitie |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US6350835B1 (fr) |
| EP (1) | EP0998456B1 (fr) |
| JP (1) | JP2001510859A (fr) |
| KR (1) | KR100553788B1 (fr) |
| CN (1) | CN1112357C (fr) |
| AT (1) | ATE234814T1 (fr) |
| AU (1) | AU8853698A (fr) |
| BR (1) | BR9810812B1 (fr) |
| CA (1) | CA2297841A1 (fr) |
| DE (1) | DE69812363T2 (fr) |
| ES (1) | ES2195373T3 (fr) |
| HU (1) | HU222505B1 (fr) |
| IL (1) | IL134162A (fr) |
| NO (1) | NO20000307L (fr) |
| PL (1) | PL338332A1 (fr) |
| SK (1) | SK284473B6 (fr) |
| TR (1) | TR200000194T2 (fr) |
| TW (1) | TW426707B (fr) |
| WO (1) | WO1999005101A1 (fr) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002076936A1 (fr) | 2001-03-23 | 2002-10-03 | Akzo Nobel N.V. | Emulsions de peroxyde organique aqueuses et stables au stockage |
| KR100984714B1 (ko) | 2002-05-08 | 2010-10-01 | 아크조 노벨 엔.브이. | 낮은 화학적 산소 요구량 값을 가지며 안정하고 안전한 고농도의 디아실 퍼옥시드와 퍼옥시디카르보네이트 유탁액 |
| FR2851245B1 (fr) * | 2003-02-14 | 2007-03-23 | Emulsion non gelee d'hydroxyperoxyester | |
| ES2797782T3 (es) * | 2006-02-10 | 2020-12-03 | Dupont Tate & Lyle Bio Products Company Llc | Composición que comprende un extracto y 1,3-propanediol de origen biológico como disolvente no irritante |
| AU2010280807B2 (en) * | 2009-08-06 | 2016-02-04 | Akzo Nobel Chemicals International B.V. | Storage stable and safe peroxide emulsions with a high active oxygen content |
| US20110152384A1 (en) * | 2009-12-17 | 2011-06-23 | Gunn Euen T | Mild leave-on skin care compositions |
| FR2995906B1 (fr) | 2012-09-21 | 2015-02-20 | Arkema France | Composition d'emulsion aqueuse de peroxyde organique |
| FR2995905B1 (fr) | 2012-09-21 | 2015-10-16 | Arkema France | Composition de peroxyde organique sans agent colloide |
| KR101845715B1 (ko) * | 2015-06-03 | 2018-04-05 | (주)제노텍 | 동결방지제 조성물 |
| BR112018016894B1 (pt) * | 2016-03-18 | 2022-06-14 | Akzo Nobel Chemicals International B.V. | Emulsão aquosa, e uso da emulsão |
| DE102019110214A1 (de) | 2019-04-17 | 2020-10-22 | Pergan Hilfsstoffe für industrielle Prozesse GmbH | Organische Peroxidemulsion, Verfahren zu deren Herstellung und deren Verwendung |
| FR3099161B1 (fr) | 2019-07-22 | 2022-10-07 | Arkema France | Emulsion aqueuse de peroxyde organique |
| EP4541788A1 (fr) * | 2023-10-20 | 2025-04-23 | Nouryon Chemicals International B.V. | Production continue d'emulsions aqueuses de peroxyde organique |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3988261A (en) | 1975-07-28 | 1976-10-26 | Ppg Industries, Inc. | Frozen organic peroxide emulsion |
| DE2629880B2 (de) * | 1976-07-02 | 1980-10-16 | Wacker-Chemie Gmbh, 8000 Muenchen | Verfahren zur Herstellung von Polyvinylchlorid nach dem Suspensionsverfahren |
| US4950422A (en) * | 1981-01-06 | 1990-08-21 | Akzona Incorporated | Peroxide emulsions containing an anti-freezing compound |
| US5260390A (en) * | 1980-01-16 | 1993-11-09 | Akzo N.V. | Peroxide emulsions containing an antifreezing compound |
| NL8000260A (nl) | 1980-01-16 | 1981-08-17 | Akzo Nv | Waterige peroxyde emulsie en de toepassing ervan in suspensie(co-)polymerisatiereacties. |
| SE435844C (sv) * | 1980-01-28 | 1989-04-17 | Kenobel Ab | Saett vid polymerisation av vinylklorid och vattendispersion foer anvaendning vid polymerisation av vinylklorid |
| JPS61130315A (ja) | 1984-11-30 | 1986-06-18 | Nippon Oil & Fats Co Ltd | 塩化ビニル系不飽和単量体の懸濁重合方法 |
| US4705888A (en) * | 1985-09-30 | 1987-11-10 | Akzo Nv | t-Alkenyl peroxy esters |
| JPH0635484B2 (ja) * | 1985-10-14 | 1994-05-11 | 化薬アクゾ株式会社 | 有機過酸化物のエマルジヨン配合物 |
| JPH01249132A (ja) * | 1988-03-31 | 1989-10-04 | Nippon Oil & Fats Co Ltd | 有機過酸化物の水性エマルション |
| SE9101674L (sv) * | 1991-05-31 | 1992-12-01 | Berol Nobel Ab | Dispersion |
-
1997
- 1997-10-30 TW TW086116204A patent/TW426707B/zh not_active IP Right Cessation
-
1998
- 1998-06-16 TR TR2000/00194T patent/TR200000194T2/xx unknown
- 1998-06-16 CA CA002297841A patent/CA2297841A1/fr not_active Abandoned
- 1998-06-16 AU AU88536/98A patent/AU8853698A/en not_active Abandoned
- 1998-06-16 IL IL13416298A patent/IL134162A/xx not_active IP Right Cessation
- 1998-06-16 BR BRPI9810812-3A patent/BR9810812B1/pt not_active IP Right Cessation
- 1998-06-16 SK SK96-2000A patent/SK284473B6/sk unknown
- 1998-06-16 AT AT98940097T patent/ATE234814T1/de not_active IP Right Cessation
- 1998-06-16 HU HU0003996A patent/HU222505B1/hu not_active IP Right Cessation
- 1998-06-16 PL PL98338332A patent/PL338332A1/xx unknown
- 1998-06-16 KR KR1020007000716A patent/KR100553788B1/ko not_active Expired - Fee Related
- 1998-06-16 EP EP98940097A patent/EP0998456B1/fr not_active Expired - Lifetime
- 1998-06-16 ES ES98940097T patent/ES2195373T3/es not_active Expired - Lifetime
- 1998-06-16 CN CN98808386A patent/CN1112357C/zh not_active Expired - Fee Related
- 1998-06-16 JP JP2000504101A patent/JP2001510859A/ja not_active Withdrawn
- 1998-06-16 WO PCT/EP1998/004015 patent/WO1999005101A1/fr not_active Ceased
- 1998-06-16 DE DE69812363T patent/DE69812363T2/de not_active Expired - Lifetime
-
2000
- 2000-01-21 NO NO20000307A patent/NO20000307L/no not_active Application Discontinuation
- 2000-01-21 US US09/489,238 patent/US6350835B1/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| ES2195373T3 (es) | 2003-12-01 |
| US6350835B1 (en) | 2002-02-26 |
| AU8853698A (en) | 1999-02-16 |
| CA2297841A1 (fr) | 1999-02-04 |
| NO20000307L (no) | 2000-03-06 |
| CN1112357C (zh) | 2003-06-25 |
| EP0998456B1 (fr) | 2003-03-19 |
| SK962000A3 (en) | 2000-09-12 |
| HUP0003996A3 (en) | 2001-04-28 |
| DE69812363T2 (de) | 2004-01-22 |
| KR20010022145A (ko) | 2001-03-15 |
| TW426707B (en) | 2001-03-21 |
| BR9810812B1 (pt) | 2010-11-30 |
| PL338332A1 (en) | 2000-10-23 |
| CN1268118A (zh) | 2000-09-27 |
| IL134162A0 (en) | 2001-04-30 |
| BR9810812A (pt) | 2000-09-12 |
| WO1999005101A1 (fr) | 1999-02-04 |
| IL134162A (en) | 2005-03-20 |
| TR200000194T2 (tr) | 2000-05-22 |
| HUP0003996A2 (en) | 2001-03-28 |
| DE69812363D1 (de) | 2003-04-24 |
| NO20000307D0 (no) | 2000-01-21 |
| KR100553788B1 (ko) | 2006-02-20 |
| HU222505B1 (hu) | 2003-07-28 |
| JP2001510859A (ja) | 2001-08-07 |
| ATE234814T1 (de) | 2003-04-15 |
| EP0998456A1 (fr) | 2000-05-10 |
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