Production and use of new thermoplastic polyurethane elastomers based on polyether carbonate polyols
US-9593199-B2 · Mar 14, 2017 · US
US11718705B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11718705-B2 |
| Application number | US-202117386844-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 28, 2021 |
| Priority date | Jul 28, 2021 |
| Publication date | Aug 8, 2023 |
| Grant date | Aug 8, 2023 |
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This invention relates to an in-situ formed polyether polyol blend having an overall functionality of 2 to 3 and an overall hydroxyl number of 40 to 220 mg KOH/g. A process for preparing these in-situ formed polyether polyol blends is also disclosed. These in-situ formed polyether polyol blends are suitable for a process of preparing viscoelastic flexible polyurethane foams.
Opening claim text (preview).
What is claimed is: 1. An in-situ formed polyether polyol blend having an overall functionality of 2 to 3, an overall hydroxyl number of 40 to 220 mg KOH/g, and comprising: (a) a monol initiated oxyalkylene ether having a hydroxyl number of less than or equal to 56 mg KOH/g polyol, and containing less than or equal to 20% of copolymerized oxyethylene, based on the total weight of monol initiated oxyalkylene ether (a); (b) a polyether polyol having a functionality of 2 to 8, a hydroxyl number of 20 to 240 mg KOH/g and containing at least 50% of copolymerized oxyethylene, based on the total weight of component (b); (c) a polyether polyol having a hydroxyl number of 80 mg KOH/g polyol to 220 mg KOH/g polyol, a nominal functionality of 2, and containing 5 to 45% of copolymerized oxyethylene, based on the total weight of polyether polyol (c); and (d) a polyether polyol having a hydroxyl number of 80 mg KOH/g polyol to 220 mg KOH/g polyol, a nominal functionality of greater than 2 to 8, and containing 5 to 45% of copolymerized oxyethylene, based on the total weight of polyether polyol (d); wherein (a) said in-situ formed polyether polyol blend comprises from 15 to 40% by weight of said monol initiated oxyalkylene ether (a), from 3 to 45% by weight of said polyether polyol (b), from 8 to 30% by weight of said polyether polyol (c), and from 20 to 60% by weight of said polyether polyol (d), with the sum of the %'s by weight of (a), (b), (c) and (d) totaling 100% by weight of said in-situ formed polyether polyol blend. 2. The in-situ formed polyether polyol blend of claim 1 , wherein said in-situ formed polyether polyol blend is phase stable. 3. The phase stable in-situ formed polyether polyol blend of claim 2 , which comprises from 15 to 40% by weight of (a) the monol initiated oxyalkylene ether; from 3 to 10% by weight of (b) the polyether polyol; from 15 to 30% by weight of (c) the polyether polyol; and from 20 to 60% by weight of (d) the polyether polyol, with the sum of the %'s by weight of (a), (b), (c) and (d) totaling 100% by weight of the phase stable in-situ formed polyether polyol blend. 4. The in-situ formed polyether polyol blend of claim 1 , wherein the monol initiated oxyalkylene ether (a) is prepared with a starter comprising a polyoxypropylene monol having a hydroxyl number of 80 mg KOH/g or less. 5. The in-situ formed polyether polyol blend of claim 1 , wherein (a) the monol initiated oxyalkylene ether comprises an oxypropylene block next to a low equivalent weight starter residue, followed by a mixed oxypropylene and oxyethylene terminal block. 6. The in-situ formed polyether polyol blend of claim 1 , wherein (b) the polyether polyol comprises a 100% oxyethylene block next to a low equivalent weight starter residue, followed by a mixed block of oxypropylene and oxyethylene. 7. The in-situ formed polyether polyol blend of claim 1 , wherein (c) the polyether polyol comprises a first mixed oxypropylene and oxyethylene block followed by a second mixed oxypropylene and oxyethylene block that has a higher copolymerized oxyethylene content compared to the copolymerized oxyethylene content of the first mixed oxypropylene and oxyethylene block. 8. The in-situ formed polyether polyol blend of claim 7 , wherein the second mixed oxypropylene and oxyethylene block of polyether polyol (c) has a copolymerized oxyethylene content that is at least 10 weight % higher than the oxyethylene content of the first mixed oxypropylene and oxyethylene block of polyether polyol (c). 9. The in-situ formed polyether polyol blend of claim 1 , wherein (d) the polyether polyol comprises a first mixed oxypropylene and oxyethylene block followed by a second mixed oxypropylene and oxyethylene block that has a higher copolymerized oxyethylene content compared to the copolymerized oxyethylene content of the first mixed oxypropylene and oxyethylene block. 10. The in-situ formed polyether polyol blend of claim 9 , wherein the second mixed oxypropylene and oxyethylene block of polyether polyol (d) has a copolymerized oxyethylene content that is at least 10 weight % higher than the oxyethylene content of the first mixed oxypropylene and oxyethylene block of polyether polyol (d). 11. A process of preparing the in-situ formed polyether polyol blend of claim 1 , comprising: I) introducing into a reaction vessel a mixture comprising: (1) an initially charged starter (S i ) comprising a monofunctional compound having a hydroxyl number of less than or equal to 80 mg KOH/g, and (2) a double metal cyanide catalyst; II) feeding (1) an epoxide comprising propylene oxide and ethylene oxide in a weight ratio of 100:0 to 80:20, into the reaction vessel; III) allowing the epoxide mixture and the initially charged starter (S i ) to react and to polymerize by feeding the epoxide until the equivalent weight of the monofunctional compound is increased by at least 10% by weight and reaches a value between 1,500 and 6,000; IV) feeding (1) an epoxide comprising propylene oxide and ethylene oxide in a weight ratio of 50:50 to 20:80, while continuously adding (2) a low equivalent weight continuously added starter (S c ) having a nominal functionality of 2 to 8, and an equivalent weight of 28 to 400, into the reaction vessel; V) completing addition of the continuously added starter (S c ); VI) allowing the mixture to continue to polymerize in the reaction vessel thereby forming (1) an intermediate in-situ formed polyether polyol blend which has an overall hydroxyl number of 10 to 200 mg KOH/g, an overall functionality of greater than 1 to 3, and which comprises (a) a monol initiated oxyalkylene ether having a hydroxyl number of less than or equal to 56 mg KOH/g, and containing less than or equal to 20% by weight of copolymerized oxyethylene, based on 100% by weight of (a), and (b) a polyether polyol having a hydroxyl number of 20 to 240 mg KOH/g, a nominal functionality of 2 to 8, and containing at least 50% by weight of copolymerized oxyethylene, based on the total weight of the polyether polyol (b); VII) feeding (1) an epoxide comprising propylene oxide and ethylene oxide in a weight ratio of 95:5 to 55:45, while continuously adding (2) a low equivalent weight continuously added starter (S c ) having a nominal functionality of 2 to 8, and an equivalent weight of 28 to 100 into the reaction vessel; VIII) completing addition of the continuously added starter (S c ) and epoxide thereby forming in addition to monol initiated oxyalkylene ether (a) and polyether polyol (b); (c) a polyether polyol having a hydroxyl number of 80 to 220 mg KOH/g polyol, a nominal functionality of 2, and containing 5 to 45% by weight of copolymerized oxyethylene, based on the total weight of the polyether polyol (c), and (d) a polyether polyol having a hydroxyl number of 80 to 220 mg KOH/g polyol, a nominal functionality of greater than 2 to 8, and containing 5 to 45% by weight of copolymerized oxyethylene, based on the total weight of polyether polyol (d). 12. The process of claim 11 , wherein the in-situ formed polyether polyol blend is phase stable. 13. The process of claim 12 , wherein the phase stable in-situ formed polyether polyol blend comprises from 15 to 40% by weight of (a) the monol initiated oxyalkylene ether; from 3 to 10% by weight of (b) the polyether polyol; from 15 to 30% by weight of (c) the polyether polyol; and from 20 to 60% by weight of (d) the polyether polyol, with the sum of the %'s by weight of (a), (b), (c) and (d) totaling 100% by weight of the phase stable in-situ formed polyether polyol blend. 14. The process of claim 11 , wherein the contin
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