U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

Process for increasing the direct esterification reaction rate of a diacid with a glycol

Patent 5015759 Issued on May 14, 1991. Estimated Expiration Date: Icon_subject December 8, 2009. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

Production of tetramethylene terephthalate polymers using 225° to 248° C. polycondensation temperature
Patent #: 4049635
Issued on: 09/20/1977
Inventor: Cleary

Process for the continuous production of high-molecular polybutyleneterephthalate Patent #: 4680376
Issued on: 07/14/1987
Inventor: Heinze ,   et al.

Inventor

Assignee

Application

No. 450911 filed on 12/08/1989

US Classes:

560/91, Polyoxyalkylene alcohol moiety528/279, Material contains a Group IVB metal atom (Ti, Zr, Hf)528/283, Material contains a Group IVA metal atom (Ge, Sn, Pb)560/90, Additional esterifying acid560/94, Preparing esters from acid or from nitrile and diol560/99, Metal containing catalyst utilized560/198, Polyoxy alcohol moiety560/204Preparing esters by esterification or carbonylation

Examiners

Primary: Dees, Jose G.
Assistant: Clarke, Vera C.

Foreign Patent References

  • 241826A3 DD. 01/13/1987
  • 51-37187 JP. 03/13/1976
  • 62-225521 JP. 10/13/1987
  • 1320621 GB. 06/13/1973

International Class

C07C 067/08

Abstract

A process for increasing the direct esterification reaction rate between a diacid and 1,4-butanediol and for directly esterifying greater than 95% of the acid ends of the diacid by mixing in any order the diacid, the 1,4-butanediol and a catalyst compound selected from organo-titanium, organo-tin, and organo-zirconium compounds, to form a reaction mixture wherein the ratio of diol:diacid is at least 2:1 and then reacting the reaction mixture at an average temperature ranging between 190° C. to 200° C. for a period of time no longer than sixty minutes. The same process may be followed substituting ethylene glycol for 1,4-butanediol, provided the catalyst compound is added neat, further provided that the average reaction temperature ranges from 190° C. to 200° C., and also provided that the reaction mixture be reacted for a period of time no longer than seventy minutes. The product resulting from this process may be polycondensed or further treated to form a high molecular weight polymer.

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