Purification of bisphenol-A

• US 4,461,915 A
• Filed: 11/15/1982
• Issued: 07/24/1984
• Est. Priority Date: 11/15/1982
• Status: Expired due to Fees

• Current Assignee: General Electric Company
• Original Assignee: General Electric Company
• Inventors: Mendiratta, Ashok K., Morgan, Wayne F.
• Primary Examiner(s): LONE, WERREN
• Application Number:
  US06/443,344
• Time in Patent Office: 617 Days
• Field of Search: 568/724
• US Class Current: 568/724
• CPC Class Codes: C07C 37/685 Processes comprising at least two steps in series
• CPC Class Codes: C07C 37/84 by crystallisation
• CPC Class Codes: C07C 39/16 Bis-(hydroxyphenyl) alkanes; Tris-(hydroxyphenyl)alkanes

Abstract

A method for purifying bisphenol-A involving aqueous crystallization of impure bisphenol-A followed by in-situ treatment of the water/bisphenol-A crystal slurry with an organic washing solvent is presented. The purified bisphenol-A is then either removed from the crystal slurry or melted so the purification process can be repeated before separating the purified bisphenol-A.

Claims

1. A process for recovering bispenol-A in a purified state from water crystallized crude bisphenol-A which comprises the steps of:

(a) mixing water-crystallized bisphenol-A in the presence of water with an organic solvent, said organic solvent being immiscible in water, lighter than water and a good solvent medium for impurities within crude bisphenol-A,

(b) agitating the mixture,

(c) forming three phases in the agitated mixture of step (b),

(d) removing the top phase of the three phase mixture of step (c), and

(e) separating purified bisphenol-A crystals from the remaining two phases of step (d).

2. A process in accordance with claim 1 wherein said organic solvent is toluene.

3. A process in accordance with claim 1 wherein said organic solvent mixed into said water crystallized bisphenol-A in the presence of water is in an amount within the range of 1 to 2 parts thereof per part of bisphenol-A on a weight basis.

4. A process for recovering bisphenol-A in a highly purified state from water crystallized crude bisphenol-A which comprises the steps of:

(a) mixing water-crystallized bisphenol-A in the presence of water with an organic solvent, said organic solvent being immiscible in water, lighter than water and a good solvent medium for impurities within crude bisphenol-A,

(b) agitating the mixture,

(c) forming three phases in the agitated mixture of step (b),

(d) removing the top phase of the three phase mixture of step (c),

(e) heating the remaining two phase crystal slurry of step (d) to a temperature sufficiently high to melt the bisphenol-A crystals within,

(f) cooling the heated two phase crystal slurry of step (e) to a temperature sufficiently low to crystallize the molten bisphenol-A,

(g) mixing a fresh organic solvent into the cooled two phase crystal slurry of step (f) said fresh organic solvent being immiscible with water, lighter than water and a good solvent medium for impurities within the bisphenol-A crystals,

(h) agitating the mixture of step (g),

(i) forming three phases in the agitated mixture of step (h),

(j) removing the top phase of the three phase mixture of step (i), and

(k) separating highly purified bisphenol-A crystals from the remaining two phases of step (j).

5. A process in accordance with claim 4 wherein said fresh organic solvent is toluene.

6. A process in accordance with claim 4 wherein the temperature selected to melt the said purified bisphenol-A crystals is within the range of 90°

C. to 100°

C.