Melt transurethane process for the preparation of polyurethanes

• US 20070117950A1
• Filed: 03/21/2006
• Published: 05/24/2007
• Est. Priority Date: 12/09/2005
• Status: Abandoned Application

• Current Assignee: Council of Scientific & Industrial Research
• Original Assignee: Council of Scientific & Industrial Research
• Inventors: Jayakannan, Manickam, Puthanparambil, Deepa
• Application Number:
  US11/386,050
• Publication Number:
  US 20070117950A1
• Time in Patent Office: Days
• US Class Current: 528/45
• CPC Class Codes: C08G 18/282 Alkanols, cycloalkanols or arylalkanols including terpenealcohols
• CPC Class Codes: C08G 18/73 acyclic
• CPC Class Codes: C08G 18/8064 with monohydroxy compounds
• CPC Class Codes: C08G 71/04 Polyurethanes

Abstract

This invention provides a melt transurethane process for the preparation of polyurethanes under solvent free melt conditions. In the transurethane process, a di-urethane monomer is reacted with diol under the melt condition in presence of catalyst like Ti (OBu)₄. The high molecular weight of the polymers are achieved by the continuous removal of low boiling alcohol like methanol from the polymerization medium under nitrogen purge and subsequently applying high vacuum. The transurethane process is demonstrated successfully for various diols units such as oligoethylene glycols, simple alkyldiols, cycloaliphatic diols and polyols. The polyurethanes are found to be soluble and thermally stable up to 300 ° C. for various high temperature applications. The thermal properties such as glass transition temperature in the polyurethanes can be easily fine-tuned by using various di-urethane and diols in the transurethane process. The present invention describes an isocyanate free polymerization route for polyurethanes under melt conditions and the transurethane process is non-hazardous and environmental friendly. The present approach is very efficient for producing high molecular weight polyurethanes and also has potential for large scale preparation.

Claims

1. A solvent free, non isocyanate, melt transurethane process for the preparation of polyurethane or its co-polymer having formula 1,

which comprise condensing di-urethane monomer with diol, in the presence of a catalyst, at a temperature in the range of 50-300°

C. to obtain the resultant melt, removing oxygen completely from the above said melt by purging it with nitrogen, under vacuum pressure of 1-0.001 mm Hg for its subsequent evacuation, under stirring, cooling and continuing the above said polymerization reaction for a period of 4-24 hrs, followed by the removal low boiling alcohols from the above said melt condensation to obtain the desired polymer, blending the resultant trans poly urethane with thermoplastics or thermosets either in solution or melt, in a molar or weight ratio of 1 to 99% to obtained the desired polymer blend.

2. A process according to claim 1, wherein the polyurethanes and its copolymers obtained are represented by a group of following types of polymer:

A-A+B—

B, A-B, A_x-B, A-B_x, A-A+B—

B+A_x-B;

A-A+B—

B+A-B_x and A-B+A_x-B or A-B+A-B_x where x=1-20 and A and B are urethane and hydroxyl functionality, respectively.

3. A process according to claim 1, wherein the di-urethane monomer used is selected from the group consisting of aromatic, aliphatic and cycloaliphatic di-urethane.

4. A process according to claim 1, wherein the aromatic di-urethane used is based on the ring structure of toluene, terephthalic, isophthalic, naphthalene or anthracene.

5. A process according to claim 1, wherein the aliphatic di-urethane monomer used is based on aliphatic units of —

(CH₂)_x—

, where x=1, 2, 3, . . . 100.

6. A process according to claim 1, wherein the cycloaliphatic di-urethane monomer used is based on mono, di, tri or multiple cycloaliphatic rings.

7. A process according to claim 6, wherein the cycloaliphatic compound used is selected from the group consisting of cyclohexyl, methylene biscyclohexyl, biscyclohexyl and tricyclodecane.

8. A process according to claim 1, wherein the diol used is selected from H(OCH₂CH₂)_xOH and HO(CH₂)_xOH, where x=1, 2, 3 ,. . . 100

9. A process according to claim 1, wherein the diol used is selected from aliphatic, cycloaliphatic and aromatic diols.

10. A process according to claim 1, wherein the cycloaliphatic diol used is selected from mono, di, tri and multiple cycloaliphatic diols.

11. A process according to claim 1, wherein the cycloaliphatic diol used is selected from the group consisting of cyclohexanedimethanol, methylene biscyclohexyl diol, biscyclohexyl diol, cyclohexane diol and tricyclodecanedimethanol.

12. A process according to claim 1, wherein the diol used is polyol containing polymer selected from the group consisting of polyesters, polyethers, polyamides, polycarbonates, polysulfones, poly acrylics, polystyrene and other thermoplastics

13. A process according to claim 1, wherein the catalyst used is selected from the group consisting of alkali, alkaline earth metal, carboxylic acid salts and a mixture thereof.

14. A process according to claim 1, wherein the catalyst used selected from the group consisting of oxides, acetates, alkoxides, phosphates, halides and coordination complexes of alkali, alkaline earth metals, transition metals, non-metals, lanthanides and actinides.

15. A process according to claim 1, wherein the amount of catalyst used is in the range 1 to 99 mole or weight percent

16. A process according to claim 1, wherein the transurethane polymer obtained has high intrinsic viscosity in the range of 0.2 to 1.0 and melt viscosity in the range of 1000 to 10,000 poise.

17. A process according to claim 1, wherein the transurethane polymer obtained has thermal stability up to 300°

C.

18. A process according to claim 1, wherein the transurethane polymer obtained has glass transition temperature in the range of −

60 to 250°

C.

19. A process according to claim 1, wherein the transurethane polymer obtained has percent crystallinity in the range of 5 to 95%

20. A process according to claim 1, wherein the transurethane polymer obtained is blended with thermoplastics or thermosets in both solution and melt in the composition range of molar or weight ratio of 1 to 99%.

21. A process according to claim 20, wherein the polyurethanes and polyurethane/thermoplastic blends obtained is either thermally processed or solution caste.

22. A process according to claim 20, wherein the thermoplastic used is selected from the group consisting of polyethylene, polyesters, polyamides, polyethers, polycarbonates, poly(vinylchloride), polystyrene, polypropylene, poly(methylmethacrylate), poly(vinylacetate), polyureas, polyurethanes, polysulfones and polyimides.