Poly(ester-carbonates) from dicarboxylic acid chlorides
AssigneeAllied Chemical Corporation
InventorsJosefina T. Baker, Robert S. Cooke, Stylianos Sifniades
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Abstract
A process for poly(ester-carbonates) from dihydric phenols, especially bisphenol A; aromatic or cycloaliphatic dicarboxylic acids, especially terephthalic acid; and phosgene as carbonate precursor wherein a reaction of the acid and phosgene is carried out in a first stage forming dicarboxylic acid chloride; and then phosgene and bisphenol A are added in separate streams, simultaneously during most of the second or condensation stage. Thereby only one kettle is required for carrying out the complete polymer production.
Claims5
In a process for production of poly(ester-carbonate) of dihydric phenol and of aromatic or cycloaliphatic dicarboxylic acid from a reaction mixture containing dichloride of at least one such acid, dissolved in a chlorinated hydrocarbon solvent inert under the reaction conditions having from 1 to 6 carbon atoms and from 1 to 4 chlorine atoms, said process employing a tertiary nitrogen base, having pK.sub.b in aqueous solution at 25.degree. C. in the range 7-11, to catalyze condensation of such dihydric phenol with said dichloride and with phosgene employed as carbonate precursor, and to serve as HCl acceptor for the HCl generated in said condensation reactions;
- the improvement which comprises:
- (1) Feeding at least one such dihydric phenol into said dichloride solution at temperature in the range 0.degree.-100.degree. C., said dichloride solution containing at the start of said condensation reaction, phosgene in the range between 10% and 50% of the stoichiometric proportion of phosgene:
- total dihydric phenol required for formation of the poly(ester-carbonate) final product with the desired mol ratio in the range 1.00:0.05 up to 1.00:0.70 of dihydric phenol:dichloride residues;
- (2) Concurrently with the feeding of dihydric phenol, agitating the reaction mixture and feeding phosgene in a separate stream thereto, until all dihydric phenol for the reaction has been added and at least 80% but not over 97% of the stoichiometrically required phosgene for reaction with all hydroxyl groups has been added;
- (3) Maintaining during the feeding of dihydric phenol, at least a 10% molar excess of tertiary nitrogen base over that required by stoichiometry;
- (4) Then allowing time for the condensation reaction forming poly(ester-carbonate) to come essentially to completion while the phosgene added is being brought at least to the stoichiometrically required quantity for reaction with all hydroxyl groups.
Dependencies are inferred from the claim text.