NO126795B - - Google Patents
Download PDFInfo
- Publication number
- NO126795B NO126795B NO451469A NO451469A NO126795B NO 126795 B NO126795 B NO 126795B NO 451469 A NO451469 A NO 451469A NO 451469 A NO451469 A NO 451469A NO 126795 B NO126795 B NO 126795B
- Authority
- NO
- Norway
- Prior art keywords
- initiator
- polymerization
- peroxydicarbonate
- vinyl
- cetyl
- Prior art date
Links
- 239000003999 initiator Substances 0.000 claims description 16
- QWVBGCWRHHXMRM-UHFFFAOYSA-N hexadecoxycarbonyloxy hexadecyl carbonate Chemical group CCCCCCCCCCCCCCCCOC(=O)OOC(=O)OCCCCCCCCCCCCCCCC QWVBGCWRHHXMRM-UHFFFAOYSA-N 0.000 claims description 11
- 150000001875 compounds Chemical class 0.000 claims description 10
- 238000006116 polymerization reaction Methods 0.000 claims description 9
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 6
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims 1
- -1 chemical compound dicetylperoxydicarbonate Chemical class 0.000 description 8
- 241000251468 Actinopterygii Species 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 229920000915 polyvinyl chloride Polymers 0.000 description 4
- 239000004800 polyvinyl chloride Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 125000005634 peroxydicarbonate group Chemical group 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- QVCQPIJMAAOGKX-UHFFFAOYSA-N (2,4,5-trimethylphenyl)thiourea Chemical compound CC1=CC(C)=C(NC(N)=S)C=C1C QVCQPIJMAAOGKX-UHFFFAOYSA-N 0.000 description 2
- 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 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-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
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000010557 suspension polymerization reaction Methods 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 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
- KTZVZZJJVJQZHV-UHFFFAOYSA-N 1-chloro-4-ethenylbenzene Chemical compound ClC1=CC=C(C=C)C=C1 KTZVZZJJVJQZHV-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 241000385654 Gymnothorax tile Species 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- ZFTFAPZRGNKQPU-UHFFFAOYSA-N dicarbonic acid Chemical compound OC(=O)OC(O)=O ZFTFAPZRGNKQPU-UHFFFAOYSA-N 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- CAEWJEXPFKNBQL-UHFFFAOYSA-N prop-2-enyl carbonochloridate Chemical compound ClC(=O)OCC=C CAEWJEXPFKNBQL-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 229920006305 unsaturated polyester 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
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
- C08F4/00—Polymerisation catalysts
- C08F4/28—Oxygen or compounds releasing free oxygen
- C08F4/32—Organic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C409/00—Peroxy compounds
- C07C409/32—Peroxy compounds the —O—O— group being bound between two >C=O groups
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polymerization Catalysts (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE1545868A SE324767B (de) | 1968-11-14 | 1968-11-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
NO126795B true NO126795B (de) | 1973-03-26 |
Family
ID=20300677
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO451469A NO126795B (de) | 1968-11-14 | 1969-11-13 |
Country Status (7)
Country | Link |
---|---|
BE (1) | BE741719A (de) |
DE (1) | DE1957434B2 (de) |
FR (1) | FR2023260A1 (de) |
GB (1) | GB1267949A (de) |
NL (1) | NL6917105A (de) |
NO (1) | NO126795B (de) |
SE (1) | SE324767B (de) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2151142A5 (de) * | 1970-08-21 | 1973-04-13 | Pennwalt Corp | |
DD106851A5 (de) * | 1972-05-24 | 1974-07-05 | ||
US4394328A (en) * | 1978-06-30 | 1983-07-19 | Ppg Industries, Inc. | Production of peroxydicarbonates |
CH656299A5 (de) * | 1982-04-15 | 1986-06-30 | Veronika Senn Walti | Bettzeug. |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2370588A (en) * | 1942-10-22 | 1945-02-27 | Pittsburgh Plate Glass Co | Organic percarbonates |
US2464062A (en) * | 1947-11-26 | 1949-03-08 | Pittsburgh Plate Glass Co | Polymerization with a peroxydicar-bonate catalyst |
NL125859C (de) * | 1962-12-07 | |||
GB978875A (de) * | 1963-03-29 | Ici Ltd |
-
1968
- 1968-11-14 SE SE1545868A patent/SE324767B/xx unknown
-
1969
- 1969-11-13 NL NL6917105A patent/NL6917105A/xx unknown
- 1969-11-13 NO NO451469A patent/NO126795B/no unknown
- 1969-11-13 FR FR6938921A patent/FR2023260A1/fr active Pending
- 1969-11-13 GB GB5561969A patent/GB1267949A/en not_active Expired
- 1969-11-14 DE DE19691957434 patent/DE1957434B2/de not_active Ceased
- 1969-11-14 BE BE741719D patent/BE741719A/xx unknown
Also Published As
Publication number | Publication date |
---|---|
GB1267949A (en) | 1972-03-22 |
BE741719A (de) | 1970-05-14 |
NL6917105A (de) | 1970-05-19 |
SE324767B (de) | 1970-06-15 |
FR2023260A1 (de) | 1970-08-07 |
DE1957434A1 (de) | 1970-06-11 |
DE1957434B2 (de) | 1978-05-18 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3108979A (en) | Emulsion polymerization with amino alcohol esters as cationic comonomers | |
NO126795B (de) | ||
US3720700A (en) | Di-cetyl peroxy dicarbonate | |
DE60128519T2 (de) | Herstellung von Polyvinylchlorid | |
GB642415A (en) | Improvements in or relating to vinyl halide polymers and copolymers and method of producing same | |
GB691908A (en) | Polymerization process | |
EP0271462B1 (de) | Perester, ihre Herstellung und Verwendung als Polymerisationsinitiatoren | |
GB847577A (en) | Method of shortstopping polymerization of mono-olefinic monomers | |
DE1618578B1 (de) | 4 4 substituierte Dycyclohexylperoxy dikarbonate und deren Herstellung | |
GB852611A (en) | Process for polymerizing vinyl compounds | |
NO761219L (de) | ||
MXPA04008432A (es) | Procedimiento de polimerizacion que incluye peroxidos de diacilo. | |
JPS5823807A (ja) | 塩化ビニルの重合方法 | |
US4093788A (en) | Method for the preparation of polyvinyl chloride by suspension or emulsion polymerization | |
US3312679A (en) | Polymerization process utilizing peroxydicarbonate ester and aminoaromatic sulfonic acid salt as catalyst | |
NO167038B (no) | Fremgangsmaate for fremstilling av en katalysatorkomponentfor anvendelse i en alfa-olefinpolymerisajonskatalysator samt anvendelse av komponenten | |
SU416952A3 (de) | ||
JPS6023765B2 (ja) | ポリ塩化ビニルの製造方法 | |
SU525708A1 (ru) | Способ получени поливинилхлорида | |
EP0049966A1 (de) | Diperesterverwendung in der Polymerisation von Vinylchlorid-Monomeren | |
JPS6332068B2 (de) | ||
IE35198B1 (en) | Cyclopropane carboxylic acid esters and a process for the manufacture thereof | |
US3801557A (en) | In-situ initiation of vinyl chloride polymers with sulfonyl peroxides | |
GB1015616A (en) | Azophosphenate compounds | |
DE2528492A1 (de) | Perester zur initiierung chemischer reaktionen |