A process for the preparation of a polycarbonate-urethane, wherein an oligocarbonate polyol is reacted with a polyisocyanate, wherein the oligocarbonate polyol is obtained by a second process comprising the steps of:
- a stage (1) of introduction, into a reactor:
- of a monomer of formula (A1):
- in which R1 and R2 are identical or different alkyl groups, or of a dimer of formula (A2):
- in which R3 and R4 are identical or different alkyl groups, or of a mixture of (A1) and (A2);
- a stage (2) of introduction, into the reactor, of a diol monomer (B1) or of a triol monomer (B2) or of a mixture of (B1) and (B2), (B1) and (B2) both being different from (A1) and (A2);
- the molar ratio in the reactor of (A1) and (A2) with respect to (B1) and (B2) corresponding to the following formula:
- [
- (
- A
-
- 1
- )
- 2
- +
- (
- A
-
- 2
- )
- 2
- ]
- [
- (
- B
-
- 1
- )
- 2
- +
- (
- B
-
- 2
- )
- 3
- ]
- <
- 1
- ,
- a subsequent stage (3) of polycondensation by transesterification of the monomers and dimers (A1), (A2), (B1) and (B2) in order to obtain an oligocarbonate polyol having a molar mass of less than 5000 g/mol and two or more hydroxyl chain end groups, and
- a stage (4) of recovery of the oligocarbonate polyol;
- wherein the diol monomer (B1) is chosen from ethylene glycol, 1,3-propanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, 1,8-octanediol or 1,10-decanediol, 1,2-propanediol, 1,3-butanediol, 2,3-butanediol, 1,3-pentanediol, 1,4-hexanediol, 2,2-dimethyl-1,3-propanediol, 3-methyl-1,5-pentanediol, 2,2-dimethyl-1,3-propanediol or 2-methyl-1,3-propanediol or from the following cyclic diols:
- cyclohexanedimethanols;
- tricyclodecanedimethanols;
- pentacyclopentanedimethanols;
- decalindimethanols;
- norbornanedimethanols;
- adamantanedimethanols,
- cyclohexanediols,
- tricyclodecanediols,
- pentacyclopentadecanediols,
- decalindiols,
- norbornanediols,
- adamantanediols,
- spiroglycol,
- 2,2,4,4-tetramethyl-1,3-cyclobutanediol;
- di-O-methylene-D-glucitol and dimethyl di-O-methylene-D-glucarate.