Polyhydroxyalkanoate Copolymers Prepared by Ring-Opening Polymerization and Related Compositions and Articles
US-2024392063-A1 · Nov 28, 2024 · US
US9624342B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9624342-B2 |
| Application number | US-2723308-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 6, 2008 |
| Priority date | Feb 6, 2008 |
| Publication date | Apr 18, 2017 |
| Grant date | Apr 18, 2017 |
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Medium and high molecular weight polyester polymers are prepared in syrup form from an ester oligomer. The oligomer is converted to the polymer by polycondensation at elevated pressure and elevated temperature in a nonreactive carrier capable of forming an azeotrope with water. The ester oligomerization or polycondensation reactions desirably are monitored using a non-viscometric technique. The process has a rapid cycle time. The syrup contains the polymer and nonreactive carrier, and may more conveniently be used to make initially non-solid products such as polyester coatings than is the case when employing pelletized solid polyester resins.
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We claim: 1. A process for preparing high molecular weight polyester syrups, which process comprises: a) providing or forming an ester oligomer in a first esterification step and substantially without ethylene glycol or propylene glycol, wherein the hydroxyl:acid or hydroxyl:ester ratio is from about 0.98:1 to about 1.1:1; b) converting the oligomer to a polyester polymer by stirring at pressure of about 34 kPa to about 100 kPa gauge and elevated temperature a reaction mixture containing the oligomer and 5 wt.% or more of a nonreactive carrier capable of forming an azeotrope with water and having a boiling point greater than that of xylenes; c) allowing the pressure to rise to about 100 kPa; and d) removing water from the reaction mixture via azeotropic reflux to provide a syrup comprising a medium high molecular weight polyester polymer in the nonreactive carrier. 2. The process according to claim 1 further comprising using a non-viscometric technique to monitor the conversion of oligomer to polymer. 3. The process according to claim 2 wherein near-IR analysis is used to monitor the disappearance of hydroxyl and acid groups. 4. The process according to claim 1 comprising forming the ester oligomer from at least one glycol having a boiling point greater than 196° C. 5. The process according to claim 1 comprising forming the ester oligomer from a glycol or glycols each having a boiling point greater than 200° C. 6. The process according to claim 1 comprising forming the ester oligomer from a glycol or glycols each having a boiling point greater than 200° C. 7. The process according to claim 1 comprising forming the ester oligomer from a glycol or glycols each having a boiling point greater than 204° C. 8. The process according to claim 1 wherein the syrup does not contain alcohols, glycols or esters that could react at polycondensation temperatures with the polymer. 9. The process according to claim 1 wherein the polymer has number average molecular weight of 4,000 to 7,000 amu. 10. The process according to claim 1 wherein the polymer has number average molecular weight of 7,001 to 30,000 amu. 11. The process according to claim 1 wherein the polymer has number average molecular weight of 8,000 to 25,000 amu. 12. The process according to claim 1 further comprising forming the ester oligomer in the nonreactive carrier. 13. The process according to claim 1 wherein the nonreactive carrier comprises an alkane, aromatic hydrocarbon, petroleum solvent, plant-derived solvent, ketone or mixture thereof. 14. The process according to claim 1 wherein the nonreactive carrier has a boiling point of up to about 300° C. 15. The process according to claim 1 wherein the nonreactive carrier has a boiling point of about 150 to about 300° C. 16. The process according to claim 1 wherein the nonreactive carrier is about 10% or more of the final syrup weight. 17. The process according to claim 1 wherein the elevated temperature is about 200 to about 260° C. 18. The process according to claim 1 wherein the elevated temperature is about 215 to about 235° C.
using solvents (C08G63/79 takes precedence) · CPC title
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