SU704944A1 - Способ получени поливинилхлорида - Google Patents
Способ получени поливинилхлоридаInfo
- Publication number
- SU704944A1 SU704944A1 SU762328148A SU2328148A SU704944A1 SU 704944 A1 SU704944 A1 SU 704944A1 SU 762328148 A SU762328148 A SU 762328148A SU 2328148 A SU2328148 A SU 2328148A SU 704944 A1 SU704944 A1 SU 704944A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- weight
- published
- polymerization
- chloroformate
- mol
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 28
- 229920000915 polyvinyl chloride Polymers 0.000 title description 20
- 239000004800 polyvinyl chloride Substances 0.000 title description 20
- 230000015572 biosynthetic process Effects 0.000 claims description 24
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 15
- FZFAMSAMCHXGEF-UHFFFAOYSA-N chloro formate Chemical compound ClOC=O FZFAMSAMCHXGEF-UHFFFAOYSA-N 0.000 claims description 13
- 229920000642 polymer Polymers 0.000 claims description 11
- -1 per 100 weight.h Chemical compound 0.000 claims description 8
- 239000003513 alkali Substances 0.000 claims description 6
- 238000010557 suspension polymerization reaction Methods 0.000 claims description 4
- 239000000084 colloidal system Substances 0.000 claims description 3
- 230000001681 protective effect Effects 0.000 claims description 2
- 241001122767 Theaceae Species 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 238000005260 corrosion Methods 0.000 claims 1
- 230000007797 corrosion Effects 0.000 claims 1
- 239000012934 organic peroxide initiator Substances 0.000 claims 1
- 238000006116 polymerization reaction Methods 0.000 description 45
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 44
- 238000003786 synthesis reaction Methods 0.000 description 19
- 239000003999 initiator Substances 0.000 description 16
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 14
- BEQKKZICTDFVMG-UHFFFAOYSA-N 1,2,3,4,6-pentaoxepane-5,7-dione Chemical compound O=C1OOOOC(=O)O1 BEQKKZICTDFVMG-UHFFFAOYSA-N 0.000 description 13
- 125000005634 peroxydicarbonate group Chemical group 0.000 description 8
- 101000945390 Homo sapiens Retinal rod rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit gamma Proteins 0.000 description 6
- 102100033597 Retinal rod rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit gamma Human genes 0.000 description 6
- RTGLJCSUKOLTEM-UHFFFAOYSA-N 2-ethylhexyl carbonochloridate Chemical compound CCCCC(CC)COC(Cl)=O RTGLJCSUKOLTEM-UHFFFAOYSA-N 0.000 description 4
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 4
- 239000008346 aqueous phase Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 4
- 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 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 3
- AOGYCOYQMAVAFD-UHFFFAOYSA-N chlorocarbonic acid Chemical class OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000011068 loading method Methods 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 2
- 229960001826 dimethylphthalate Drugs 0.000 description 2
- CWINGZLCRSDKCL-UHFFFAOYSA-N ethoxycarbonyloxy ethyl carbonate Chemical compound CCOC(=O)OOC(=O)OCC CWINGZLCRSDKCL-UHFFFAOYSA-N 0.000 description 2
- 230000000977 initiatory effect Effects 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical group C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- DPUFBNYQARGKJG-UHFFFAOYSA-N C(C1=CC=CC=C1)(=O)OCCOC(=O)Cl Chemical compound C(C1=CC=CC=C1)(=O)OCCOC(=O)Cl DPUFBNYQARGKJG-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 101001009086 Pseudomonas fluorescens Hydroxycinnamoyl-CoA hydratase-lyase Proteins 0.000 description 1
- 241000218998 Salicaceae Species 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229940043430 calcium compound Drugs 0.000 description 1
- 150000001674 calcium compounds Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- BLCKNMAZFRMCJJ-UHFFFAOYSA-N cyclohexyl cyclohexyloxycarbonyloxy carbonate Chemical compound C1CCCCC1OC(=O)OOC(=O)OC1CCCCC1 BLCKNMAZFRMCJJ-UHFFFAOYSA-N 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000012933 diacyl peroxide Substances 0.000 description 1
- 125000003438 dodecyl group Chemical group [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])* 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 150000003388 sodium compounds Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
Landscapes
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU762328148A SU704944A1 (ru) | 1976-02-26 | 1976-02-26 | Способ получени поливинилхлорида |
| YU48077A YU39088B (en) | 1976-02-26 | 1977-02-21 | Process for the production of polyvinyl chloride |
| FI770592A FI61705C (fi) | 1976-02-26 | 1977-02-23 | Foerfarande foer framstaellning av polyvinylklorid |
| DK79577A DK146340C (da) | 1976-02-26 | 1977-02-23 | Fremgangsmaade til fremstilling af polyvinylchlorid |
| NO770629A NO146163C (no) | 1976-02-26 | 1977-02-24 | Fremgangsmaate til fremstilling av polyvinylklorid |
| CS123777A CS189330B1 (en) | 1976-02-26 | 1977-02-24 | Process for preparing polyvinylchloride |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU762328148A SU704944A1 (ru) | 1976-02-26 | 1976-02-26 | Способ получени поливинилхлорида |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU704944A1 true SU704944A1 (ru) | 1979-12-25 |
Family
ID=20650125
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU762328148A SU704944A1 (ru) | 1976-02-26 | 1976-02-26 | Способ получени поливинилхлорида |
Country Status (6)
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2288234C1 (ru) * | 2005-09-22 | 2006-11-27 | Открытое акционерное общество "Пласткард" | Способ суспензионной полимеризации винилхлорида |
| RU2443717C2 (ru) * | 2006-04-27 | 2012-02-27 | Аркема Франс | Способ свободнорадикальной полимеризации или сшивания в присутствии выбранного органического пероксида, полученного способом ex situ |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FI940630A7 (fi) * | 1994-02-11 | 1995-08-12 | Ahlstroem Pumput Oy | Keskipakopumppu |
-
1976
- 1976-02-26 SU SU762328148A patent/SU704944A1/ru active
-
1977
- 1977-02-21 YU YU48077A patent/YU39088B/xx unknown
- 1977-02-23 DK DK79577A patent/DK146340C/da not_active IP Right Cessation
- 1977-02-23 FI FI770592A patent/FI61705C/fi not_active IP Right Cessation
- 1977-02-24 NO NO770629A patent/NO146163C/no unknown
- 1977-02-24 CS CS123777A patent/CS189330B1/cs unknown
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2288234C1 (ru) * | 2005-09-22 | 2006-11-27 | Открытое акционерное общество "Пласткард" | Способ суспензионной полимеризации винилхлорида |
| RU2443717C2 (ru) * | 2006-04-27 | 2012-02-27 | Аркема Франс | Способ свободнорадикальной полимеризации или сшивания в присутствии выбранного органического пероксида, полученного способом ex situ |
Also Published As
| Publication number | Publication date |
|---|---|
| NO146163B (no) | 1982-05-03 |
| DK146340C (da) | 1984-02-27 |
| YU39088B (en) | 1984-04-30 |
| FI61705B (fi) | 1982-05-31 |
| DK79577A (da) | 1977-08-27 |
| DK146340B (da) | 1983-09-12 |
| FI770592A7 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1977-08-27 |
| CS189330B1 (en) | 1979-04-30 |
| NO146163C (no) | 1982-08-11 |
| NO770629L (no) | 1977-08-29 |
| YU48077A (en) | 1982-05-31 |
| FI61705C (fi) | 1982-09-10 |
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