NO752264L - - Google Patents
Info
- Publication number
- NO752264L NO752264L NO75752264A NO752264A NO752264L NO 752264 L NO752264 L NO 752264L NO 75752264 A NO75752264 A NO 75752264A NO 752264 A NO752264 A NO 752264A NO 752264 L NO752264 L NO 752264L
- Authority
- NO
- Norway
- Prior art keywords
- polyvinyl chloride
- dispersion
- water vapor
- vinyl chloride
- evaporation rate
- Prior art date
Links
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 86
- 239000004800 polyvinyl chloride Substances 0.000 claims description 84
- 239000006185 dispersion Substances 0.000 claims description 56
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 55
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 50
- 238000001704 evaporation Methods 0.000 claims description 43
- 230000008020 evaporation Effects 0.000 claims description 43
- 238000000034 method Methods 0.000 claims description 32
- 238000007872 degassing Methods 0.000 claims description 22
- 239000000178 monomer Substances 0.000 claims description 19
- 238000010438 heat treatment Methods 0.000 claims description 6
- 230000008569 process Effects 0.000 claims description 5
- 238000009835 boiling Methods 0.000 claims description 4
- 230000009471 action Effects 0.000 claims description 2
- 238000010943 off-gassing Methods 0.000 description 33
- -1 diacetyl- Chemical compound 0.000 description 10
- 238000006116 polymerization reaction Methods 0.000 description 10
- 229920000642 polymer Polymers 0.000 description 9
- 239000000725 suspension Substances 0.000 description 9
- 239000002253 acid Substances 0.000 description 7
- 229920001577 copolymer Polymers 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- 230000009467 reduction Effects 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 5
- 238000001035 drying Methods 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 3
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 3
- 229920003086 cellulose ether Polymers 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 238000009792 diffusion process Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000005187 foaming Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229920005862 polyol Polymers 0.000 description 3
- 150000003077 polyols Chemical class 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 230000007306 turnover Effects 0.000 description 3
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 108010010803 Gelatin Proteins 0.000 description 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- 150000001447 alkali salts Chemical class 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 229920000159 gelatin Polymers 0.000 description 2
- 239000008273 gelatin Substances 0.000 description 2
- 235000019322 gelatine Nutrition 0.000 description 2
- 235000011852 gelatine desserts Nutrition 0.000 description 2
- 229920000578 graft copolymer Polymers 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 229920002689 polyvinyl acetate Polymers 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 238000004904 shortening Methods 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000010557 suspension polymerization reaction Methods 0.000 description 2
- 229920001897 terpolymer Polymers 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 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
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 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
- 239000004908 Emulsion polymer Substances 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- BSVQJWUUZCXSOL-UHFFFAOYSA-N cyclohexylsulfonyl ethaneperoxoate Chemical compound CC(=O)OOS(=O)(=O)C1CCCCC1 BSVQJWUUZCXSOL-UHFFFAOYSA-N 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 239000004815 dispersion polymer Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000010556 emulsion polymerization method Methods 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- MEGHWIAOTJPCHQ-UHFFFAOYSA-N ethenyl butanoate Chemical compound CCCC(=O)OC=C MEGHWIAOTJPCHQ-UHFFFAOYSA-N 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000010559 graft polymerization reaction Methods 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 125000005395 methacrylic acid group Chemical class 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 150000002976 peresters Chemical class 0.000 description 1
- 229920002857 polybutadiene Polymers 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
- 239000000843 powder Substances 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- KQYLUTYUZIVHND-UHFFFAOYSA-N tert-butyl 2,2-dimethyloctaneperoxoate Chemical compound CCCCCCC(C)(C)C(=O)OOC(C)(C)C KQYLUTYUZIVHND-UHFFFAOYSA-N 0.000 description 1
- OPQYOFWUFGEMRZ-UHFFFAOYSA-N tert-butyl 2,2-dimethylpropaneperoxoate Chemical compound CC(C)(C)OOC(=O)C(C)(C)C OPQYOFWUFGEMRZ-UHFFFAOYSA-N 0.000 description 1
- SWAXTRYEYUTSAP-UHFFFAOYSA-N tert-butyl ethaneperoxoate Chemical compound CC(=O)OOC(C)(C)C SWAXTRYEYUTSAP-UHFFFAOYSA-N 0.000 description 1
- BWSZXUOMATYHHI-UHFFFAOYSA-N tert-butyl octaneperoxoate Chemical compound CCCCCCCC(=O)OOC(C)(C)C BWSZXUOMATYHHI-UHFFFAOYSA-N 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 229920002554 vinyl polymer Polymers 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
- C08F6/00—Post-polymerisation treatments
- C08F6/14—Treatment of polymer emulsions
- C08F6/16—Purification
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymerisation Methods In General (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2441303A DE2441303A1 (de) | 1974-08-29 | 1974-08-29 | Verfahren zur entfernung von vinylchlorid aus waessrigen polyvinylchloriddispersionen |
| DE19742442931 DE2442931B2 (de) | 1974-09-07 | 1974-09-07 | Verfahren zur entfernung von nicht umgesetztem vinylchlorid aus waessrigen polyvinylchlorid-dispersionen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO752264L true NO752264L (es) | 1976-03-02 |
Family
ID=25767612
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO75752264A NO752264L (es) | 1974-08-29 | 1975-06-25 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US4017445A (es) |
| JP (1) | JPS5150992A (es) |
| BR (1) | BR7505508A (es) |
| CH (1) | CH602798A5 (es) |
| ES (1) | ES440531A1 (es) |
| FI (1) | FI752405A (es) |
| FR (1) | FR2283153A1 (es) |
| GB (1) | GB1510339A (es) |
| IT (1) | IT1041531B (es) |
| NL (1) | NL7510183A (es) |
| NO (1) | NO752264L (es) |
| SE (1) | SE7509426L (es) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5126988A (ja) * | 1974-08-30 | 1976-03-05 | Sumitomo Chemical Co | Enkabinirukeijugotaichunizanzonsuru enkabinirutanryotai no jokyohoho |
| FR2305446A1 (fr) * | 1975-03-28 | 1976-10-22 | Rhone Poulenc Ind | Procede ameliore de degazage des polymeres et copolymeres prepares par polymerisation en masse d'une composition monomere a base de chlorure de vinyle |
| DE2521780C2 (de) * | 1975-05-16 | 1982-10-21 | Hoechst Ag, 6000 Frankfurt | Verfahren zur kontinuierlichen Entfernung von Monomeren aus einer wäßrigen Dispersion eines Polymeren |
| US4168373A (en) * | 1975-11-24 | 1979-09-18 | Borden, Inc. | Removal of residual vinyl chloride monomer from polyvinyl chloride latex |
| JPS5283404A (en) * | 1975-12-29 | 1977-07-12 | Mitsubishi Monsanto Chem Co | Elimination of monomers |
| JPS5283405A (en) * | 1975-12-29 | 1977-07-12 | Mitsubishi Monsanto Chem Co | Elimination of monomers |
| US4375541A (en) * | 1976-07-14 | 1983-03-01 | Stauffer Chemical Company | Method for separating vinyl chloride from polymers |
| DE2640546C2 (de) * | 1976-09-09 | 1982-07-01 | Hoechst Ag, 6000 Frankfurt | Verfahren zur kontinuierlichen Entfernung von Vinylchlorid aus einer wässerigen Dispersion von Homo- und Copolymerisaten des Vinylchlorids |
| DE2722952C2 (de) * | 1977-05-20 | 1982-06-09 | Wacker-Chemie GmbH, 8000 München | Verfahren zur schonenden Entgasung von koagulationsempfindlichen Polyvinylchlorid-Latices |
| JPS548693A (en) * | 1977-06-21 | 1979-01-23 | Chisso Corp | Removal of monomer from vinyl chloride resin slurry by steam treatment using improved plate column |
| DE2744462C2 (de) * | 1977-10-03 | 1982-09-16 | Wacker-Chemie GmbH, 8000 München | Verfahren zur Verhinderung der Schaumbildung bei der Restmonomerentfernung aus wäßrigen Polymerdispersionen |
| US4151141A (en) * | 1977-11-16 | 1979-04-24 | The Dow Chemical Company | Process for continuously removing volatile organic material from aqueous dispersions of synthetic polymers |
| DE2757168A1 (de) * | 1977-12-22 | 1979-07-05 | Wacker Chemie Gmbh | Verfahren zur verringerung des monomergehaltes in scherkraftempfindlichen und/oder temperaturempfindlichen polymerdispersionen |
| US4529753A (en) * | 1984-04-10 | 1985-07-16 | Polysar Limited | Chemical/steam stripping |
| JP3724012B2 (ja) * | 1995-08-04 | 2005-12-07 | チッソ株式会社 | 残留モノマー除去装置およびそれを用いる残留モノマー除去方法 |
| CN101501079B (zh) * | 2006-08-03 | 2011-09-14 | 巴塞尔聚烯烃股份有限公司 | 聚烯烃精制法 |
| WO2008015228A2 (en) * | 2006-08-03 | 2008-02-07 | Basell Polyolefine Gmbh | Process for the polyolefin finishing |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2662867A (en) * | 1951-03-29 | 1953-12-15 | Goodrich Co B F | Method of stabilizing aqueous dispersions of haloethylene polymers |
| BE579094A (es) * | 1958-05-30 | |||
| US3129132A (en) * | 1960-04-14 | 1964-04-14 | Arne R Gudheim | Treatment of latex |
| US3371059A (en) * | 1963-02-21 | 1968-02-27 | Teknika Inc | Monomer stripping |
| DE1248943C2 (de) * | 1965-07-20 | 1974-03-07 | Basf Ag | Verfahren und Vorrichtung zur diskontinuierlichen Entfernung von Geruchs-stoffen auswaessrigen Polymerisatdispersionen |
-
1975
- 1975-06-25 NO NO75752264A patent/NO752264L/no unknown
- 1975-08-25 SE SE7509426A patent/SE7509426L/xx unknown
- 1975-08-26 FR FR7526231A patent/FR2283153A1/fr active Granted
- 1975-08-27 CH CH1110875A patent/CH602798A5/xx not_active IP Right Cessation
- 1975-08-27 IT IT51076/75A patent/IT1041531B/it active
- 1975-08-27 FI FI752405A patent/FI752405A/fi not_active Application Discontinuation
- 1975-08-28 JP JP50104499A patent/JPS5150992A/ja active Pending
- 1975-08-28 NL NL7510183A patent/NL7510183A/xx not_active Application Discontinuation
- 1975-08-28 ES ES440531A patent/ES440531A1/es not_active Expired
- 1975-08-28 GB GB35515/75A patent/GB1510339A/en not_active Expired
- 1975-08-28 BR BR7505508*A patent/BR7505508A/pt unknown
- 1975-08-28 US US05/608,791 patent/US4017445A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| US4017445A (en) | 1977-04-12 |
| JPS5150992A (es) | 1976-05-06 |
| SE7509426L (sv) | 1976-03-01 |
| CH602798A5 (es) | 1978-08-15 |
| FR2283153B1 (es) | 1979-05-18 |
| FI752405A (es) | 1976-03-01 |
| BR7505508A (pt) | 1976-08-03 |
| GB1510339A (en) | 1978-05-10 |
| ES440531A1 (es) | 1977-05-16 |
| NL7510183A (nl) | 1976-03-02 |
| FR2283153A1 (fr) | 1976-03-26 |
| IT1041531B (it) | 1980-01-10 |
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