BE581249A - - Google Patents
Info
- Publication number
- BE581249A BE581249A BE581249DA BE581249A BE 581249 A BE581249 A BE 581249A BE 581249D A BE581249D A BE 581249DA BE 581249 A BE581249 A BE 581249A
- Authority
- BE
- Belgium
- Prior art keywords
- emi
- polycarbonate
- organic solvent
- high molecular
- molecular weight
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
- C08G64/16—Aliphatic-aromatic or araliphatic polycarbonates
- C08G64/1608—Aliphatic-aromatic or araliphatic polycarbonates saturated
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyesters Or Polycarbonates (AREA)
Description
<EMI ID=1.1>
La présente invention se rapporte à des polycarbonates à poids moléculaire élevé et concerne plus
<EMI ID=2.1>
diols aromatiques et de diols aliphatiques, principalement de diols primaires. Elle concerne particulièrement
<EMI ID=3.1>
et de diols aliphatiques.
Suivant l'invention on procure des polycarbona-
<EMI ID=4.1>
<EMI ID=5.1>
<EMI ID=6.1>
<EMI ID=7.1>
<EMI ID=8.1>
<EMI ID=9.1>
<EMI ID=10.1>
<EMI ID=11.1>
<EMI ID=12.1>
ae 5 à 35.
<EMI ID=13.1>
les valences non satisfaites étant satisfaites par les
<EMI ID=14.1>
<EMI ID=15.1> <EMI ID=16.1>
particulièrement heureux et les pro uits résultants sont particulièrement or-':cieux.
Il ne faut que des petites quantités de phosg�ne
<EMI ID=17.1>
ayant des résidus alternés de Bisphénol A et n'éthylène glycol est prolongé en chaîne avec une petite quantité de phosgène en présence d'une base pour donner un polycarbo-
<EMI ID=18.1>
<EMI ID=19.1> <EMI ID=20.1>
prenant dans l'agent liquide un solvant organique inerte.
<EMI ID=21.1>
moles de diol aromatique par mole de bishaloformate on arrive à des produits qui se polymérisent plus effectivement à la phosgénation. Tout diol aromatique n'ayant pas réagi peut si on le désire être enlevé avant la polymérisation en profitant de sa solubilité dans l'eau dans des solutions alcalines aqueuses.
<EMI ID=22.1>
Ainsi sauf pour les avantages économiques et de manipula-tion, toute température est convenable pourvu ou 'elle
<EMI ID=23.1>
à conseiller d'éviter une volatilisation indésirable
du solvant et/ou des dispositifs de réaction fermés ainsi que la solidification ce l'agent de réaction. Des températures sont choisies en fonction de ces considéra-
<EMI ID=24.1>
res de 0 à 40[deg.]C.
La réaction elle-même nécessite deux équivalents
<EMI ID=25.1>
diverses raisons on utilise ordinairement de 2,1 à 4,0 moles d'hyuroxyde de sodium ou d'équivalent. car mole de
<EMI ID=26.1> <EMI ID=27.1>
de agitée de polycarbonate et de solution aqueuse d'alcalin inorganique par exemple l'hydroxyde de sodium. Il c ;vient aussi d'ajouter un soldant organique insoluble
<EMI ID=28.1>
sans lequel à la fois le polycarbonate originel et le polycarbonate constituant le produit est soluble. Des
<EMI ID=29.1> glycol en quantité ae 1,1 sole à un m�lan'e abrité de 1,0
<EMI ID=30.1>
<EMI ID=31.1>
<EMI ID=32.1> <EMI ID=33.1> <EMI ID=34.1>
qui en résultent sont réalisés avec ':les polycarbonates
non
<EMI ID=35.1>
cyclohexane.
<EMI ID=36.1> <EMI ID=37.1>
Il est possible de produire des polycarbonates
à chaîne étendue comme considéré ici par l'addition simul-
<EMI ID=38.1>
ne tout en contrôlant soigneusement les conditions et les taux des réactifs.
Les valeurs de K dont question ici étaient obtenues en pesant 0,2500 g de polycarbonate dans un [pound]'la- <EMI ID=39.1>
<EMI ID = 1.1>
The present invention relates to high molecular weight polycarbonates and relates to more
<EMI ID = 2.1>
aromatic diols and aliphatic diols, mainly primary diols. It particularly concerns
<EMI ID = 3.1>
and aliphatic diols.
According to the invention, polycarbona-
<EMI ID = 4.1>
<EMI ID = 5.1>
<EMI ID = 6.1>
<EMI ID = 7.1>
<EMI ID = 8.1>
<EMI ID = 9.1>
<EMI ID = 10.1>
<EMI ID = 11.1>
<EMI ID = 12.1>
ae 5 to 35.
<EMI ID = 13.1>
the unfulfilled valences being satisfied by the
<EMI ID = 14.1>
<EMI ID = 15.1> <EMI ID = 16.1>
particularly happy and the resulting products are particularly golden - ': heavens.
It only takes small amounts of phosg � ne
<EMI ID = 17.1>
having alternating residues of Bisphenol A and ethylene glycol is chain-extended with a small amount of phosgene in the presence of a base to give a polycarbo-
<EMI ID = 18.1>
<EMI ID = 19.1> <EMI ID = 20.1>
taking in the liquid agent an inert organic solvent.
<EMI ID = 21.1>
moles of aromatic diol per mole of bishaloformate we arrive at products which polymerize more effectively on phosgenation. Any unreacted aromatic diol can if desired be removed prior to polymerization by taking advantage of its water solubility in aqueous alkaline solutions.
<EMI ID = 22.1>
So except for the economic and handling advantages, any temperature is suitable provided it
<EMI ID = 23.1>
advisable to avoid unwanted volatilization
of the solvent and / or closed reaction devices as well as the solidification of the reaction agent. Temperatures are chosen according to these considerations.
<EMI ID = 24.1>
res from 0 to 40 [deg.] C.
The reaction itself requires two equivalents
<EMI ID = 25.1>
For various reasons, 2.1 to 4.0 moles of sodium hyuroxide or the like are ordinarily used. because mole of
<EMI ID = 26.1> <EMI ID = 27.1>
of stirred polycarbonate and aqueous solution of inorganic alkali for example sodium hydroxide. It has also just added an insoluble organic solvent
<EMI ID = 28.1>
without which both the original polycarbonate and the polycarbonate constituting the product are soluble. Of
<EMI ID = 29.1> glycol in quantity ae 1.1 sole at a m � lan'e sheltered from 1.0
<EMI ID = 30.1>
<EMI ID = 31.1>
<EMI ID = 32.1> <EMI ID = 33.1> <EMI ID = 34.1>
which result are produced with ': polycarbonates
no
<EMI ID = 35.1>
cyclohexane.
<EMI ID = 36.1> <EMI ID = 37.1>
It is possible to produce polycarbonates
extended chain as considered here by the simul-
<EMI ID = 38.1>
do while carefully controlling the conditions and rates of the reagents.
The K values in question here were obtained by weighing 0.2500 g of polycarbonate in a [pound] 'la- <EMI ID = 39.1>
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US1235634XA | 1958-08-01 | 1958-08-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
BE581249A true BE581249A (en) |
Family
ID=22409411
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BE581249D BE581249A (en) | 1958-08-01 |
Country Status (2)
Country | Link |
---|---|
BE (1) | BE581249A (en) |
FR (1) | FR1235634A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2827325A1 (en) * | 1978-06-22 | 1980-01-10 | Bayer Ag | METHOD FOR THE PRODUCTION OF ALIPHATIC-AROMATIC POLYCARBONATES WITH DIPHENOL CARBONATE END GROUPS AND THE USE THEREOF FOR THE PRODUCTION OF THERMOPLASTICALLY PROCESSABLE, HIGHLY MOLECULAR, SEGMENTED, ALIPHATIC-AROMATIC-AROMATIC-AROMATIC-AROMATIC-AROMATIC-AROMATIC |
-
0
- BE BE581249D patent/BE581249A/fr unknown
-
1959
- 1959-07-07 FR FR799504A patent/FR1235634A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
FR1235634A (en) | 1960-07-08 |
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