Poly(2-hydroxyalkanoic acid) and method of its manufacture
View Patent ↗A method for manufacturing poly(2-hydroxyalkanoic acid) included the steps of a) mixing a cyclic diester of a 2-hydroxyalkanoic acid and a polymerization catalyst, b) polymerizing the cyclic diester to form poly(2-hydroxyalkanoic acid) in liquid phase, c) adding a phosphoric acid ester as a catalyst deactivating agent to the liquid phase, d) applying a devolatilization step to the liquid phase, and e) allowing the poly(2-hydroxyalkanoic acid) to solidify. The catalyst deactivating agent is added after the devolatilization step is applied. The method results in an improved melt stability of the manufactured polymer.
1. Method for manufacturing polylactic acid, comprising the steps of mixing a lactide of a 2-hydroxyalkanoic acid and a polymerization catalyst, polymerizing the lactide to form polylactic acid in liquid phase, adding a phosphoric acid ester as a catalyst deactivating agent to the liquid phase, applying a devolatilisation step to the liquid phase, and allowing the polylactic acid to solidify, wherein the catalyst deactivating agent is added after the devolatilisation step is applied.
2. Method according to claim 1 , wherein the phosphoric acid ester comprises an alkanoic acid phosphate compound.
3. Method according to claim 1 , wherein an end-capping agent is added to the polylactic acid in the liquid phase.
4. Method according to claim 3 , wherein the end-capping agent is added in the liquid phase after at least 90% by weight of the lactide is converted into the corresponding polylactic acid.
5. Method according to claim 3 , wherein the end-capping agent and the catalyst deactivating agent are added to the polylactic acid in the liquid phase at different stages of the polymerization process.
6. Method according to claim 3 , wherein the end-capping agent is added prior to the deactivating agent.
7. Method according to claim 3 , wherein the end-capping agent is an anhydride.
8. Method according to claim 7 , wherein the anhydride is at least one selected from the group consisting of phthalic acid anhydride, acetic acid anhydride and succinic acid anhydride.
9. Method according to claim 3 , wherein the amount of added end-capping agent to the polylactic acid in liquid phase is in the range between 0.1 and 4 molar excess as compared to the amount of hydroxyl end groups.
10. Method according to claim 1 , wherein an additional devolatilisation step is applied on the formed polylactic acid in liquid phase after the addition of the deactivating agent.
11. Polylactic acid obtainable with the method according to claim 1 , wherein the polymer has a M n , relative to Polystyrene Standards ranging between 20000 and 500000 g/mol,
wherein the concentration of cyclic diester in the corresponding polymer is less than 0.5% by weight, and
wherein its weight decrease in liquid phase at 250° C. during a period of 1 hour is less than 2% by weight.
12. Polylactic acid according to claim 11 , wherein it comprises phosphorus in an amount ranging between 5-1000 ppm.
13. Method according to claim 3 , wherein the end-capping agent is added in the liquid phase after at least 95% by weight of the lactide is converted into the corresponding polylactic acid.
14. Method according to claim 3 , wherein the end-capping agent is added in the liquid phase after at least 97% by weight of the lactide is converted into the corresponding polylactic acid.
15. Method according to claim 3 , wherein the amount of added end-capping agent to the polylactic acid in liquid phase is in the range between 0.5 and 2 molar excess as compared to the amount of hydroxyl end groups.
16. Method according to claim 3 , wherein the amount of added end-capping agent to the polylactic acid in liquid phase is in the range between 0.8 and 1.5 molar excess as compared to the amount of hydroxyl end groups.
17. Polylactic acid according to claim 11 , wherein the concentration of lactide in the corresponding polymer is less than 0.3% by weight.
18. Polylactic acid according to claim 11 , wherein its weight decrease in liquid phase at 250° C. during a period of 1 hour is less than 1.5% by weight.
19. Method according to claim 2 , wherein alkanoic acid of the alkanoic acid phosphate compound is stearic acid.