BE455982A - Procede pour influencer les phenomenes de polymerisation ainsi que les proprietes des produits obtenus - Google Patents
Procede pour influencer les phenomenes de polymerisation ainsi que les proprietes des produits obtenusInfo
- Publication number
- BE455982A BE455982A BE455982DA BE455982A BE 455982 A BE455982 A BE 455982A BE 455982D A BE455982D A BE 455982DA BE 455982 A BE455982 A BE 455982A
- Authority
- BE
- Belgium
- Prior art keywords
- properties
- well
- products obtained
- vinyl
- influencing
- Prior art date
Links
- 238000000034 method Methods 0.000 title description 3
- 238000006116 polymerization reaction Methods 0.000 title description 3
- 239000000203 mixture Substances 0.000 description 5
- IYNRVIKPUTZSOR-HWKANZROSA-N ethenyl (e)-but-2-enoate Chemical compound C\C=C\C(=O)OC=C IYNRVIKPUTZSOR-HWKANZROSA-N 0.000 description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
- 239000004342 Benzoyl peroxide Substances 0.000 description 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 235000019400 benzoyl peroxide Nutrition 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 230000035939 shock Effects 0.000 description 2
- 229920001567 vinyl ester resin Polymers 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 241000157302 Bison bison athabascae Species 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002485 inorganic esters Chemical class 0.000 description 1
- 235000015110 jellies Nutrition 0.000 description 1
- 239000008274 jelly Substances 0.000 description 1
- 150000002895 organic esters Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 150000002976 peresters Chemical class 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 238000003303 reheating Methods 0.000 description 1
- 239000002904 solvent Substances 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
- C08F214/00—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
- C08F214/02—Monomers containing chlorine
- C08F214/04—Monomers containing two carbon atoms
- C08F214/06—Vinyl chloride
-
- 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
- C08F18/00—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 an acyloxy radical of a saturated carboxylic acid, of carbonic acid or of a haloformic acid
- C08F18/02—Esters of monocarboxylic acids
- C08F18/04—Vinyl esters
-
- 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
- C08F18/00—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 an acyloxy radical of a saturated carboxylic acid, of carbonic acid or of a haloformic acid
- C08F18/02—Esters of monocarboxylic acids
- C08F18/04—Vinyl esters
- C08F18/08—Vinyl acetate
-
- 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
- C08F2/00—Processes of polymerisation
- C08F2/04—Polymerisation in solution
- C08F2/06—Organic solvent
-
- 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
- C08F36/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
- C08F36/02—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
- C08F36/20—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds unconjugated
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)
Description
Procédé pour influencer les phénomènes de polymérisation ainsi que les propriétés des produits obtenus. Au brevet principal, on a décrit un procédé pour fabriquer des polymériaats de haute valeur à partir d'esters organiques et inorganiques de l'aloool vinylique par polymérisation en présence de crotonate de vinyle. Lors ' du traitement ultérieur, on a trouTé maintenant qu'on peut obtenir à partir d'esters de vinyle et d'une addition de crotonate de vinyle des produits d'un genre nouveau particulièrement désirés au point de vue technique, en polymérisant un mélange des deux esters de vinyle en l'absenoe de solvants à l'aide de combinaisons peroxydées on présenoe <EMI ID=1.1> binaison peroxydée, outre le peroxyde de benzoyle, l'ester peraoétique tel qu'il est obtenu par oxydation d'aoétaldéhyde à faible teneur en cobalt par de l'oxygène moléculaire à environ 0[deg.] convient surtout très bien. Grâce à une addl-tion de crotonate allant jusqu'à quelques pourcents, on obtient des produits exempts de bulles, limpides comme du Terre, coriaces à température ordinaire, apte à résis- ter à un choc ou à un coup, et qui peuvent par exemple être employés comme Terre organique. Exemple 1.- Un mélange de 91 parties en poids d'acétate de vinyle et 2 parties de crotonate de vinyle est ajouté à <EMI ID=2.1> Le mélange est déjà, après quelques heures, pris en une gelée transparente . Elle duroit graduellement, après quoi elle est enlevée du vase de verre cylindrique. , l'air, la masse devient après un court repos si dure qu'elle ne peut être marquée par l'ongle. Elle est très coriace et apte à résister en toute circonstance aux coups et auxohocs. Par réchauffage à haute température par <EMI ID=3.1> Exemple 2. Un mélange de 91 parties en poids d'acétate de vinyle et 4 parties de orotonate de vinyle est polymérisé avec 5 parties de la solution du perester mentionnée plus haut, à 50 - 60[deg.]. On obtient un polymérisat dur et transparent. Exemple 3.- 'Un mélange de 91 parties en poids d'acétate de vinyle et 2 parties de crotonate de vinyle est polymérisé avec 0,5 partie de peroxyde de benzoyle avec addition simultanée <EMI ID=4.1> duit limpide comme le verre est relativement dur et durci <EMI ID=5.1> dans l'exemple ci-dessus. Ce produit également est très coriace. sans aoétaldéhyde, on n'a pas pu obtenir des produits aussi homogènes, aussi clairs et à la fois aussi durs.
Claims (1)
- <EMI ID=6.1><EMI ID=7.1>
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE233502X | 1940-01-05 | ||
| DE226694X | 1940-01-05 | ||
| CH226694T | 1941-01-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE455982A true BE455982A (fr) | 1944-06-30 |
Family
ID=61628528
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE440208D BE440208A (fr) | 1940-01-05 | 1941-01-03 | Procede pour influencer les phenomenes de polymerisation ainsi que les proprietes des produits obtenus |
| BE455982D BE455982A (fr) | 1940-01-05 | 1944-05-26 | Procede pour influencer les phenomenes de polymerisation ainsi que les proprietes des produits obtenus |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE440208D BE440208A (fr) | 1940-01-05 | 1941-01-03 | Procede pour influencer les phenomenes de polymerisation ainsi que les proprietes des produits obtenus |
Country Status (4)
| Country | Link |
|---|---|
| BE (2) | BE440208A (fr) |
| CH (4) | CH233501A (fr) |
| DE (2) | DE874214C (fr) |
| FR (2) | FR881719A (fr) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3005809A (en) * | 1957-09-05 | 1961-10-24 | Air Reduction | Vinyl alcohol-crotonic acid copolymers |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB496276A (en) * | 1937-05-27 | 1938-11-28 | Ig Farbenindustrie Ag | Manufacture of artificial substances resembling rubber |
-
1940
- 1940-01-06 DE DEP3643D patent/DE874214C/de not_active Expired
-
1941
- 1941-01-03 BE BE440208D patent/BE440208A/fr unknown
- 1941-01-03 CH CH233501D patent/CH233501A/de unknown
- 1941-01-03 CH CH226694D patent/CH226694A/de unknown
- 1941-01-03 CH CH233502D patent/CH233502A/de unknown
- 1941-05-29 FR FR881719D patent/FR881719A/fr not_active Expired
-
1943
- 1943-05-29 DE DEP5489D patent/DE881260C/de not_active Expired
-
1944
- 1944-05-26 BE BE455982D patent/BE455982A/fr unknown
- 1944-05-26 FR FR53726D patent/FR53726E/fr not_active Expired
- 1944-05-27 CH CH295895D patent/CH295895A/de unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DE874214C (de) | 1953-04-20 |
| CH233502A (de) | 1944-07-31 |
| BE440208A (fr) | 1941-02-28 |
| CH233501A (de) | 1944-07-31 |
| CH226694A (de) | 1943-04-30 |
| FR881719A (fr) | 1943-05-06 |
| CH295895A (de) | 1954-01-15 |
| FR53726E (fr) | 1946-07-29 |
| DE881260C (de) | 1953-06-29 |
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