Method for producing a mixture of alkoxylated polyphenols and use of said mixture
US-2024409679-A1 · Dec 12, 2024 · US
US9527976B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9527976-B2 |
| Application number | US-201514964684-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 10, 2015 |
| Priority date | May 21, 2009 |
| Publication date | Dec 27, 2016 |
| Grant date | Dec 27, 2016 |
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An embodiment of a closed-cell polymeric rigid foam may be made using a one-shot method and a reaction system that includes a hydrofluoroalkene physical blowing agent and a polyol mixture having an aminic polyol. The hydrofluoroalkene blowing agent has 3 to 5 carbon atoms and a boiling point between 10° C. and 40° C. at 1 atmosphere pressure. Embodiments of rigid foams may have high closed cell content and are particularly well suited for thermal insulation.
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The invention claimed is: 1. A process for preparing a rigid polymeric foam having a closed cell content of greater than 85% and a density of less than 4.5 pounds per cubic foot, wherein the process comprises reacting: (a) an isocyanate composition comprising one or more organic polyisocyanates; and (b) an isocyanate reactive composition comprising: (i) a first polyol, wherein the first polyol is a aminic polyol selected from the group consisting of aromatic amine-initiated polyols, Mannich polyols, and mixtures thereof; and wherein the first polyol comprises an alkylene oxide moiety; and (ii) a second polyol having a nominal hydroxyl functionality of at least 2 and a molecular weight of from 60 to 10,000 that is different than the first polyol and is free of amine groups, wherein either the isocyanate composition or the isocyanate reactive composition further comprises one or more alkane blowing agents and one or more hydrofluoroalkene blowing agents selected from the group consisting of 2-bromopentafluoropropene, 1-bromopentafluoropropene, 3-bromopentafluoropropene, 3,3,4,4,5,5,5-heptafluoro-1-pentene, 3-bromo-1,1,3,3-tetrafluoropropene, 2-bromo-1,3,3,3-tetrafluoropropene, 1-bromo-2,3,3,3-tetrafluoropropene, 1,1,2,3,3,4,4-heptafluorobut-1-ene, 2-bromo-3,3,3-trifluoropropene, E-1-bromo-3,3,3-trifluoropropene-1,3,3,3-trifluoro-2-(trifluoromethy)propene, 1-chloro-3,3,3-trifluoropropene, 2-chloro-3,3,3-trifluoropropene, and 1,1,1-trifluoro-2-butene; and wherein the weight ratio of the first polyol to the second polyol is from 90:10 to 40:60 and the combined weights of the first polyol and the second polyol is at least 30% of the total weight of the reaction system. 2. The process of claim 1 , wherein the alkane blowing agents comprise n-pentane, isopentane, cyclopentane, and combinations thereof. 3. The process of claim 2 , wherein the alkane blowing agents comprise isopentane, cyclopentane, and combinations thereof. 4. The process of claim 1 , wherein a polyol blend comprises the first polyol and the second polyol and wherein the polyol blend has a OH value of 400 mg KOH/g. 5. The process of claim 1 , wherein the aromatic amine-initiated polyol has a nominal hydroxyl functionality of at least 2 and a molecular weight of greater than 300 and less than 10,000. 6. The process of claim 1 , wherein the Mannich polyol has a nominal hydroxyl functionality of at least 2, has a molecular weight of greater than 150 and less than 10,000, and contains at least one secondary or tertiary amine nitrogen atom. 7. The process of claim 1 , wherein the isocyanate reactive composition further comprises one or more chemical blowing agents. 8. The process of claim 7 , wherein the one or more chemical blowing agents is water. 9. The process of claim 8 , wherein water comprises at least 0.2% and less than 5% by weight based on the total weight of components (a) and (b). 10. The process according to claim 1 , wherein the alkylene oxide moiety comprises ethylene oxide, propylene oxide, butylene oxide, or combinations thereof. 11. The process according to claim 1 , wherein the alkylene oxide moiety comprises ethylene oxide, propylene oxide, or combinations thereof. 12. The process according to claim 1 , wherein the alkylene oxide moiety comprises ethylene oxide. 13. A rigid polyurethane or polyisocyanurate foam having a closed cell content closed cell content of greater than 85% and a density of less than 4.5 pounds per cubic foot, wherein the foam is the reaction product of: (a) an organic polyisocyanate composition; and (b) an isocyanate reactive composition comprising: (i) a first polyol, wherein the first polyol is an aminic polyol selected from the group consisting of aromatic amine-initiated polyols, Mannich polyols, and mixtures thereof; and wherein the first polyol comprises an alkylene oxide moiety; (ii) a second polyol having a nominal hydroxyl functionality of at least 2 and a molecular weight of from 60 to 10,000 that is different than the first polyol and is free of amine groups; and (iii) a blowing agent composition comprising one or more alkanes and one or more hydrofluoroalkene blowing agents selected from the group consisting of 2-bromopentafluoropropene, 1-bromopentafluoropropene, 3-bromopentafluoropropene, 3,3,4,4,5,5,5-heptafluoro-1-pentene, 3-bromo-1,1,3,3-tetrafluoropropene, 2-bromo-1,3,3,3-tetrafluoropropene, 1-bromo-2,3,3,3-tetrafluoropropene, 1,1,2,3,3,4,4-heptafluorobut-1-ene, 2-bromo-3,3,3-trifluoropropene, E-1-bromo-3,3,3-trifluoropropene-1,3,3,3-trifluoro-2-(trifluoromethyl)propene, 1-chloro-3,3,3-trifluoropropene, 2-chloro-3,3,3-trifluoropropene, and 1,1,1-trifluoro-2-butene, and wherein the weight ratio of the first polyol to the second polyol is from 90:10 to 40:60 and the combined weights of the first polyol and the second polyol is at least 30% of the total weight of the reaction system. 14. The rigid polyurethane or polyisocyanurate foam of claim 13 , wherein the alkane comprises n-pentane, isopentane, cyclopentane, and combinations thereof. 15. The rigid polyurethane or polyisocyanurate foam of claim 14 , wherein the alkane comprise isopentane, cyclopentane, and combinations thereof. 16. The rigid polyurethane or polyisocyanurate foam of claim 13 , wherein the aromatic amine-initiated polyol has a nominal hydroxyl functionality of at least 2 and a molecular weight of greater than 300 and less than 10,000. 17. The rigid polyurethane or polyisocyanurate foam of claim 13 , wherein the Mannich polyol has a nominal hydroxyl functionality of at least 2, has a molecular weight of greater than 150 and less than 10,000, and contains at least one secondary or tertiary amine nitrogen atom. 18. The rigid polyurethane or polyisocyanurate foam of claim 13 , wherein the isocyanate reactive composition further comprises one or more chemical blowing agents. 19. The rigid polyurethane or polyisocyanurate foam of claim 18 , wherein the one or more chemical blowing agents is water. 20. The rigid polyurethane or polyisocyanurate foam of claim 13 , wherein water comprises at least 0.2% and less than 5% by weight based on the total weight of components (a) and (b). 21. The rigid polyurethane or polyisocyanurate foam of claim 13 , wherein a polyol blend comprises the first polyol and the second polyol and wherein the polyol blend has a OH value of 400 mg KOH/g. 22. The rigid polyurethane or polyisocyanurate foam according to claim 13 , wherein the alkylene oxide moiety comprises ethylene oxide, propylene oxide, butylene oxide, or combinations thereof. 23. The rigid polyurethane or polyisocyanurate foam according to claim 13 , wherein the alkylene oxide moiety comprises ethylene oxide, propylene oxide, or combinations thereof. 24. The rigid polyurethane or polyisocyanurate foam according to claim 13 , wherein the alkylene oxide moiety comprises ethylene oxide.
having alkylene polyamine groups · CPC title
from polyesters · CPC title
containing carbon, halogen and hydrogen only · CPC title
Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors · CPC title
having carbocyclic groups · CPC title
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