Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Isophthalic Acid | HCID 8496 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | Phenol, 4,4'-(1-methylethylidene)bis-, 1,1'-diacetate | HCID 82437 | — |
| Edukt | HCID 18669760 | HCID 18669760 | — |
| Edukt | 2,6-Dimethylphenol chloroform ethanol | HCID 131711879 | — |
| Produkt | Bisphenol A | HCID 6623 | — |
Reaktionsschritte
An equimolar mixture of 2,2-bis(4-acetoxyphenyl)propane (Bisphenol A diacetate) and isophthalic acid is heated gradualy to 290° C. in a stirred vessel under gradually increasing vacuum to remove the acetic acid which is liberated. When the melt viscosity of the condensate reaches a level such that stirring becomes difficult the melt is drained from the reaction vessel and crystallized. The crystallized polymer is subjected to solid state polymerization under vacuum at 280° C. until the inherent viscosity reaches 0.65 dl/g (in 40/60 by weight tetrachloroethane/phenol solution at 25° C.). The polymer is then extruded at 350° C. and pelletized. The polymer has an inherent viscosity of 0.62 and a carboxylic acid content of 40 microequivalents per gram (μeq./g), determined by potentiometric titration of a solution of the polymer in a 2,6-dimethylphenol/chloroform/ethanol mixture with an ethanolic solution of potassium hydroxide.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04222932 |
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| Quelldatensatz | uspto-grants-1980_09 |
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| ORD ID | ord-da044c87e1ee442cbdf8d9c420ead15b |
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| Quellennotiz | uspto-grants-1980_09 |
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