Catalyzed interfacial polycondensation polycarbonate process

• US 4,515,936 A
• Filed: 04/16/1984
• Issued: 05/07/1985
• Est. Priority Date: 04/16/1984
• Status: Expired due to Fees

• Current Assignee: General Electric Company
• Original Assignee: General Electric Company
• Inventors: Yeboah, Yaw D., Sikdar, Subhas K.
• Primary Examiner(s): NOT, DEFINED
• Application Number:
  US06/600,634
• Time in Patent Office: 386 Days
• Field of Search: 528/196, 528/198, 528/199, 528/200, 524/841, 524/714, 524/745
• US Class Current: 528/200
• CPC Class Codes: C08G 64/24 and phenols

Abstract

This invention relates to a catalyzed interfacial polycondensation aromatic polycarbonate process which comprises forming an agitated two-phase mixture comprising an organic solvent phase with catalyst and an aqueous phase containing an aromatic dihydroxy compound, a base and an ionic surfactant. A carbonyl halide is added to the mixture and reacted with the aromatic dihydroxy compound to form an aromatic polycarbonate. The aromatic polycarbonate is recovered from the aqueous phase.

Claims

1. A method of producing aromatic polycarbonate by a catalyzed interfacial polycondensation polycarbonate process comprising

(1) forming an agitated two-phase admixture comprising

(i) an organic phase containing an inert organic solvent and a polycondensation catalyst,

(ii) an aqueous phase containing dissolved therein an aromatic dihydroxy compound, a strong base and an ionic surfactant in a quantity of from about 100 to 1,000 parts per million having a pH of at least 11 subject to the proviso that

(a) the volume ratio of inert organic solvent phase to aqueous phase is within the range of from about 0.04:

1 to 0.20;

1 and

(b) the mole ratio of base to aromatic dihydroxy compound is at least about 0.25;

1,

(2) adding and reacting a carbonyl halide with the aromatic dihydroxy compound to form an aromatic polycarbonate having a weight average molecular weight of at least about 2000, and

(3) separating and recovering the solid aromatic polycarbonate particulate from the liquid aqueous phase.

2. The claim 1 process wherein the aromatic dihydroxy compound has the formula, ##STR7## wherein R_f is selected from (a) a group of hydrocarbon linkages consisting of alkylene, alkylidene, cycloalkylene, cycloalkylidene and arylene linkage and mixtures thereof, and (b) a linkage selected from the group consisting of ether, carbonyl, amine, sulfur and phosphorous linkages;

Ar and Ar'"'"' are arene radicals;

Y is a monovalent radical selected from bromine, chlorine, alkyl and alkoxy radicals;

each d represents a whole number from zero up to a maximum equivalent to the number of replaceable hydrogens substituted on the aromatic rings comprising Ar and Ar'"'"', subject to the proviso that when d is equal to 2 or more, no more than one Y group is ortho-positioned relative to an OH group;

X is a monovalent radical selected from the group consisting of bromine, chlorine, alkyl, aryl, and cycloalkyl radicals and mixtures thereof;

e represents a whole number of from zero to a maximum of the number of replaceable hydrogens on R_f ;

aa, bb and cc represent whole numbers including zero, with the proviso that when bb is not zero, neither aa nor cc are zero, and when bb is zero, aa or cc but not both include zero.

3. The claim 2 process wherein the dihydric phenol is of the formulas ##STR8## where independently each R'"'"' is selected from the group consisting of hydrogen, bromine, chlorine, alkyl radicals of from 1 to 4 carbon atoms and alkoxy radicals of from 1 to 4 carbon atoms, R_g and R_h are selected from the group consisting of hydrogen and alkyl radicals of from 1 to 2 carbon atoms, each Z_a is selected from the group consisting of hydrogen, chlorine and bromine, subject to the proviso that at least one Z_a is chlorine or bromine.

4. The claim 3 process wherein a non-sterically-hindered aromatic dihydroxy compound is present as a major portion relative to a minor portion of sterically-hindered aromatic dihydroxy compound.

5. The claim 4 process wherein the non-sterically-hindered aromatic dihydroxy compound is at least 90 mole percent.

6. The claim 5 process wherein the non-sterically-hindered dihydroxy compound is bis(4-hydroxyphenyl)-propane-2,2, and the base is an alkali metal hydroxide.

7. The claim 6 process wherein the bis(4-hydroxy-phenyl)propane-2,2 portion is 100 mole %, said inert organic solvent is methylene chloride, a phenol chain stopper is added to the organic phase, said polycondensation catalyst is triethylamine, said base is sodium hydroxide, the aqueous phase pH is within the range of from 11.0 to 14.0, the mole ratio of sodium hydroxide to bisphenol-A is within the range of from about 1:

1 to 4.0;

1, and the aromatic polycarbonate produced has a M_W within the range of from about 5000 to 100,000 with a M_W /M_N ratio within the range from about 2.00 to 3.75 and an intrinsic viscosity above 0.40 dl/g.

8. The claim 6 process wherein the pH is at least about 12.

9. The method as in claim 1 wherein said organic phase also contains a chain stopper.

10. The method as in claim 11 wherein said chain stopper is phenol.

11. A method as in claim 1 wherein the ionic surfactant is selected from the group consisting of sodium lauryl sulfate, dodecyl-trimethylammonium bromide and cetyltrimethylammonium bromide.

12. A method as in claim 11 wherein the surfactant is utilized in a quantity within the range of about 400-600 parts/million per aqueous phase.

13. A method as in claim 12 wherein the ionic surfactant utilized is sodium lauryl sulfate in a quantity of about 500 parts/million of the aqueous phase.

14. A method as in claim 7 wherein the ionic surfactant is selected from the group consisting of sodium lauryl sulfate, dodecyl-trimethylammonium bromide and cetyltrimethylammonium bromide.

15. A method as in claim 14 wherein the surfactant is utilized in a quantity within the range of about 400-600 parts/million per aqueous phase.

16. A method as in claim 15 wherein the ionic surfactant utilized is sodium lauryl sulfate in a quantity of about 500 parts/million of the aqueous phase.