PL110001B1 - Method of producing polyvinyl chloride by suspension polymerization - Google Patents
Method of producing polyvinyl chloride by suspension polymerization Download PDFInfo
- Publication number
- PL110001B1 PL110001B1 PL1978205165A PL20516578A PL110001B1 PL 110001 B1 PL110001 B1 PL 110001B1 PL 1978205165 A PL1978205165 A PL 1978205165A PL 20516578 A PL20516578 A PL 20516578A PL 110001 B1 PL110001 B1 PL 110001B1
- Authority
- PL
- Poland
- Prior art keywords
- initiator
- polymerization
- tank
- vinyl chloride
- water
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 42
- 229920000915 polyvinyl chloride Polymers 0.000 title claims description 9
- 239000004800 polyvinyl chloride Substances 0.000 title claims description 9
- 238000010557 suspension polymerization reaction Methods 0.000 title description 2
- 239000003999 initiator Substances 0.000 claims description 59
- 238000006116 polymerization reaction Methods 0.000 claims description 55
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 44
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 33
- 229920000642 polymer Polymers 0.000 claims description 14
- 239000000725 suspension Substances 0.000 claims description 14
- 239000003381 stabilizer Substances 0.000 claims description 11
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 9
- 239000001301 oxygen Substances 0.000 claims description 9
- 229910052760 oxygen Inorganic materials 0.000 claims description 9
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 7
- 238000006243 chemical reaction Methods 0.000 claims description 6
- BWJUFXUULUEGMA-UHFFFAOYSA-N propan-2-yl propan-2-yloxycarbonyloxy carbonate Chemical compound CC(C)OC(=O)OOC(=O)OC(C)C BWJUFXUULUEGMA-UHFFFAOYSA-N 0.000 claims description 6
- 239000007900 aqueous suspension Substances 0.000 claims description 5
- 238000002156 mixing Methods 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 3
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 3
- BSVQJWUUZCXSOL-UHFFFAOYSA-N cyclohexylsulfonyl ethaneperoxoate Chemical group CC(=O)OOS(=O)(=O)C1CCCCC1 BSVQJWUUZCXSOL-UHFFFAOYSA-N 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims description 3
- 239000003960 organic solvent Substances 0.000 claims description 3
- 125000005498 phthalate group Chemical class 0.000 claims description 3
- 150000001350 alkyl halides Chemical class 0.000 claims description 2
- 239000007789 gas Substances 0.000 claims description 2
- 230000000379 polymerizing effect Effects 0.000 claims description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 4
- 238000011049 filling Methods 0.000 description 4
- 238000011068 loading method Methods 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 230000002028 premature Effects 0.000 description 4
- 238000005096 rolling process Methods 0.000 description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 3
- 229960002380 dibutyl phthalate Drugs 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- GTJOHISYCKPIMT-UHFFFAOYSA-N 2-methylundecane Chemical compound CCCCCCCCCC(C)C GTJOHISYCKPIMT-UHFFFAOYSA-N 0.000 description 2
- SGVYKUFIHHTIFL-UHFFFAOYSA-N Isobutylhexyl Natural products CCCCCCCC(C)C SGVYKUFIHHTIFL-UHFFFAOYSA-N 0.000 description 2
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 2
- 230000002776 aggregation Effects 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- VKPSKYDESGTTFR-UHFFFAOYSA-N isododecane Natural products CC(C)(C)CC(C)CC(C)(C)C VKPSKYDESGTTFR-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920002689 polyvinyl acetate Polymers 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 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
- ZACVGCNKGYYQHA-UHFFFAOYSA-N 2-ethylhexoxycarbonyloxy 2-ethylhexyl carbonate Chemical compound CCCCC(CC)COC(=O)OOC(=O)OCC(CC)CCCC ZACVGCNKGYYQHA-UHFFFAOYSA-N 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- LQKBKHFGCGFBAF-UHFFFAOYSA-N butyl carboxyoxy carbonate Chemical group CCCCOC(=O)OOC(O)=O LQKBKHFGCGFBAF-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 230000009849 deactivation Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- BUXJGUZPQJRBAY-UHFFFAOYSA-N hexylsulfonyl ethaneperoxoate Chemical compound C(CCCCC)S(=O)(=O)OOC(C)=O BUXJGUZPQJRBAY-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 238000005507 spraying Methods 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
- 230000007704 transition Effects 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J4/00—Feed or outlet devices; Feed or outlet control devices
- B01J4/02—Feed or outlet devices; Feed or outlet control devices for feeding measured, i.e. prescribed quantities of reagents
-
- 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
- C08F14/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen
- C08F14/02—Monomers containing chlorine
- C08F14/04—Monomers containing two carbon atoms
- C08F14/06—Vinyl chloride
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymerisation Methods In General (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19772710121 DE2710121A1 (de) | 1977-03-09 | 1977-03-09 | Verfahren zur herstellung von polyvinylchlorid durch suspensionspolymerisation |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| PL205165A1 PL205165A1 (pl) | 1979-02-12 |
| PL110001B1 true PL110001B1 (en) | 1980-06-30 |
Family
ID=6003095
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL1978205165A PL110001B1 (en) | 1977-03-09 | 1978-03-08 | Method of producing polyvinyl chloride by suspension polymerization |
Country Status (9)
| Country | Link |
|---|---|
| AR (1) | AR224860A1 (de) |
| BE (1) | BE864680A (de) |
| DD (1) | DD134535A5 (de) |
| DE (1) | DE2710121A1 (de) |
| FR (1) | FR2383203A1 (de) |
| GB (1) | GB1574572A (de) |
| IT (1) | IT1101981B (de) |
| PL (1) | PL110001B1 (de) |
| YU (1) | YU54478A (de) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4395478B2 (ja) * | 2003-12-26 | 2010-01-06 | 信越化学工業株式会社 | 塩化ビニル系重合体の製造方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1439957A (fr) * | 1964-03-26 | 1966-05-27 | Monsanto Co | Perfectionnements apportés à la polymérisation de monomères vinyliques |
| US3451985A (en) * | 1964-03-26 | 1969-06-24 | Monsanto Co | Method of polymerizing vinyl monomers |
| DE2442574A1 (de) * | 1974-09-05 | 1976-03-25 | Huels Chemische Werke Ag | Verfahren zur herstellung von polyvinylchlorid unter vermeiden von vinylchlorid-emissionen durch diskontinuierliche polymerisation in suspension |
-
1977
- 1977-03-09 DE DE19772710121 patent/DE2710121A1/de not_active Withdrawn
-
1978
- 1978-03-03 GB GB8544/78A patent/GB1574572A/en not_active Expired
- 1978-03-07 AR AR271342A patent/AR224860A1/es active
- 1978-03-07 IT IT48319/78A patent/IT1101981B/it active
- 1978-03-07 DD DD78204015A patent/DD134535A5/de not_active IP Right Cessation
- 1978-03-08 PL PL1978205165A patent/PL110001B1/pl unknown
- 1978-03-08 BE BE185759A patent/BE864680A/xx not_active IP Right Cessation
- 1978-03-08 YU YU00544/78A patent/YU54478A/xx unknown
- 1978-03-09 FR FR7806859A patent/FR2383203A1/fr active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| IT1101981B (it) | 1985-10-07 |
| FR2383203A1 (fr) | 1978-10-06 |
| DD134535A5 (de) | 1979-03-07 |
| DE2710121A1 (de) | 1978-09-14 |
| PL205165A1 (pl) | 1979-02-12 |
| GB1574572A (en) | 1980-09-10 |
| IT7848319A0 (it) | 1978-03-07 |
| FR2383203B1 (de) | 1981-06-12 |
| AR224860A1 (es) | 1982-01-29 |
| YU54478A (en) | 1982-06-30 |
| BE864680A (fr) | 1978-09-08 |
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