Protein-containing foams, manufacture and use thereof
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
C08G-018/64
C08G-018/00
출원번호
US-0719721
(2010-03-08)
등록번호
US-8623931
(2014-01-07)
발명자
/ 주소
Parker, Anthony A.
Marcinko, Joseph J.
출원인 / 주소
Biopolymer Technologies, Ltd.
대리인 / 주소
Goodwin Procter LLP
인용정보
피인용 횟수 :
7인용 특허 :
63
초록
The invention relates generally to protein-containing polyurethane foams, methods and compositions for making the polyurethane foams, and articles comprising the polyurethane foams.
대표청구항▼
1. A polyurethane foam comprising a reaction product of a mixture comprising: (a) an isocyanate-based reactant;(b) an optional isocyanate-reactive compound; and(c) an isolated, water-soluble polypeptide composition that is capable of stabilizing a polyurethane-based foam, wherein the composition com
1. A polyurethane foam comprising a reaction product of a mixture comprising: (a) an isocyanate-based reactant;(b) an optional isocyanate-reactive compound; and(c) an isolated, water-soluble polypeptide composition that is capable of stabilizing a polyurethane-based foam, wherein the composition comprises one or more of the following features: (a) an amide-I absorption band between about 1633 cm−1 and 1680 cm−1, as determined by solid state FTIR;(b) an amide-II band between approximately 1522 cm−1 and 1560 cm−1, as determined by solid state FTIR;(c) two prominent 1° amide N—H stretch absorption bands centered at about 3200 cm−1, and at about 3300 cm−1, as determined by solid state FTIR;(d) a prominent cluster of protonated nitrogen nuclei defined by 15N chemical shift boundaries at about 94 ppm and at about 100 ppm, and 1H chemical shift boundaries at about 7.6 ppm and at about 8.1 ppm, as determined by solution state, two-dimensional proton-nitrogen coupled NMR;(e) an average molecular weight of between about 600 and about 2,500Daltons;(f) an inability to stabilize an oil-in-water emulsion, wherein, when an aqueous solution comprising 14 parts by weight of protein dissolved or dispersed in 86 parts by weight of water is admixed with 14 parts by weight of PMDI, the aqueous solution and the PMDI produce an unstable suspension that macroscopically phase separates under static conditions within five minutes after mixing;(g) the water-soluble polypeptide composition is capable of stabilizing a polyurethane-based foam relative to a polyurethane-based foam created from the same starting composition lacking the water soluble protein composition; or(h) the water-soluble polypeptide composition is capable of reducing the density of a polyurethane-based foam by at least 5% relative to a polyurethane-based foam created from the same starting composition lacking the water-soluble polypeptide composition;wherein the foam is substantially free of water-insoluble/water dispersible polypeptides. 2. The polyurethane foam of claim 1, wherein the isocyanate-based reactant is an organic polyisocyanate. 3. The polyurethane foam of claim 2, wherein the organic polyisocyanate is polymeric diphenylmethane diisocyanate, 2,4-tolylene diisocyanate, 2,6-tolylene diisocyanate, benzene diisocyanate, m-xylylene diisocyanate, 1,4-phenylene diisocyanate, 1,3-phenylene diisocyanate, 4,4′-diphenyl diisocyanate, 4,4′-diphenyldimethylmethane diisocyanate, hexamethylene diisocyanate, tolidine diisocyanate, dianisidine diisocyanate, 1,5-naphthalene diisocyanate, 1,4-cyclohexane diisocyanate, or a combination thereof. 4. The polyurethane foam of claim 1, wherein the isocyanate-based reactant comprises a urethane, allophanate, urea, biuret, carbodiimide, uretonimine, isocyanurate, or a combination thereof. 5. The polyurethane foam of claim 1, wherein the isocyanate-based reactant is polymeric diphenylmethane diisocyanate. 6. The polyurethane foam of claim 1, wherein the isocyanate-reactive compound is present and is nucleophilically reactive with an isocyanate. 7. The polyurethane foam of claim 6, wherein the isocyanate-reactive compound is a compound having a hydroxyl group or an amino group capable of reacting with the isocyanate. 8. The polyurethane foam of claim 1, wherein the isocyanate-reactive compound is present and is a polyol. 9. The polyurethane foam of claim 1, wherein the isocyanate-reactive compound is present and is a polyol derived from castor oil, linseed oil, or soy oil. 10. The polyurethane foam of claim 1, wherein the isocyanate-reactive compound is present and is a polyol initiated with a compound selected from the group consisting of glycerol, trimethylopropane, triethanolamine, pentaerythritol, sorbitol sucrose, diamine, tolylene diamine, diaminodiphenylmethane, a polymethylene polyphenylene polyamine, ethanolamine, diethanolamine, or a mixture thereof. 11. The polyurethane foam of claim 1, wherein the isocyanate-reactive compound is present and is a hydroxyl terminated polythioether, polyamide, polyesteramide, polycarbonate, polyacetal, polyolefin or polysiloxane, or is a polyester obtained by condensation of a glycol or higher functionality polyol with a dicarboxylic acid. 12. The polyurethane foam of claim 1, wherein the isocyanate-reactive compound is present and is polyoxypropylene glycol, polypropylene oxide-ethylene oxide, propylene glycol, propane diol, glycerin, an amine alkoxylate, or a mixture thereof. 13. The polyurethane foam of claim 1, wherein the isocyanate-reactive compound is present and is polyoxypropylene glycol. 14. The polyurethane foam of claim 1, wherein the mixture further comprises a surfactant. 15. The polyurethane foam of claim 1, wherein the foam has a density in the range of from about 0.01 g/cm3 to about 0.5 g/cm3 as determined by ASTM D-7487. 16. The polyurethane foam of claim 1, wherein the foam has a density that is from 5% to 80% less dense than a foam created from the same starting composition lacking the water-soluble polypeptide composition. 17. The polyurethane foam of claim 1, wherein the foam cream time, as defined by ASTM D-7487, is less than one minute. 18. The polyurethane foam of claim 1, wherein the foam free rise height, as determined by ASTM D7487, is greater than the foam free rise height of a foam created from the same starting composition lacking the water-soluble polypeptide composition. 19. The polyurethane foam of claim 18, wherein the foam free rise height is at least 5% greater than the foam free rise height of a foam created from the same starting composition lacking the water-soluble polypeptide composition. 20. The polyurethane foam of claim 1, wherein the foam has a larger number of small, uniform cells when compared to a foam created from the same starting composition lacking the water-soluble polypeptide composition. 21. A method of producing a polyurethane foam, comprising the steps of: (a) mixing a protein containing composition and an isocyanate-based reactant to produce a mixture; and(b) permitting the mixture to produce a polyurethane foam, wherein the protein containing composition is an isolated, water-soluble polypeptide composition that is capable of stabilizing a polyurethane-based foam, wherein the isolated, water-soluble polypeptide composition comprises one or more of the following features: (a) an amide-I absorption band between about 1633 cm−1 and 1680 cm−1, as determined by solid state FTIR;(b) an amide-II band between approximately 1522 cm−1 and 1560 cm−1, as determined by solid state FTIR;(c) two prominent 1° amide N—H stretch absorption bands centered at about 3200 cm−1, and at about 3300 cm−1, as determined by solid state FTIR;(d) a prominent cluster of protonated nitrogen nuclei defined by 15N chemical shift boundaries at about 94 ppm and at about 100 ppm, and 1H chemical shift boundaries at about 7.6 ppm and at about 8.1 ppm, as determined by solution state, two-dimensional proton-nitrogen coupled NMR;(e) an average molecular weight of between about 600 and about 2,500 Daltons;(f) in an inability to stabilize an oil-in-water emulsion, wherein, when an aqueous solution comprising 14 parts by weight of protein dissolved or dispersed in 86 parts by weight of water is admixed with 14 parts by weight of PMDI, the aqueous solution and the PMDI produce an unstable suspension that macroscopically phase separates under static conditions within five minutes after mixing;(g) the water-soluble polypeptide composition is capable of stabilizing a polyurethane-based foam relative to a polyurethane-based foam created from the same starting composition lacking the water soluble protein composition; or(h) the water-soluble polypeptide composition is capable of reducing the density of a polyurethane-based foam by at least 5% relative to a polyurethane-based foam created from the same starting composition lacking the water-soluble polypeptide composition;wherein the foam is substantially free of water-insoluble/water dispersible polypeptides. 22. The method of claim 21, wherein the protein containing composition is an isolated, water-soluble polypeptide composition that is capable of stabilizing a polyurethane-based foam, wherein the composition comprises the following features: (a) an amide-I absorption band between about 1633 cm−1 and 1680 cm−1, as determined by solid state FTIR;(b) an amide-II band between approximately 1522 cm−1 and 1560 cm−1, as determined by solid state FTIR;(c) two prominent 1° amide N—H stretch absorption bands centered at about 3200cm−1, and at about 3300 cm−1, as determined by solid state FTIR;(d) a prominent cluster of protonated nitrogen nuclei defined by 15N chemical shift boundaries at about 94 ppm and at about 100 ppm, and 1H chemical shift boundaries at about 7.6 ppm and at about 8.1 ppm, as determined by solution state, two-dimensional proton-nitrogen coupled NMR;(e) an average molecular weight of between about 600 and about 2,500 Daltons;(f) an inability to stabilize an oil-in-water emulsion, wherein, when an aqueous solution comprising 14 parts by weight of protein dissolved or dispersed in 86parts by weight of water is admixed with 14 parts by weight of PMDI, the aqueous solution and the PMDI produce an unstable suspension that macroscopically phase separates under static conditions within five minutes after mixing;(g) the water-soluble polypeptide composition is capable of stabilizing a polyurethane-based foam relative to a polyurethane-based foam created from the same starting composition lacking the water soluble protein composition; and(h) the water-soluble polypeptide composition is capable of reducing the density of a polyurethane-based foam by at least 5% relative to a polyurethane-based foam created from the same starting composition lacking the water-soluble polypeptide composition. 23. The method of claim 21, wherein the mixture in step (a) further comprises an isocyanate-reactive compound. 24. The method of claim 21, wherein the isocyanate-based reactant is an organic polyisocyanate. 25. The method of claim 24, wherein the organic polyisocyanate is polymeric diphenylmethane diisocyanate, 2,4-tolylene diisocyanate, 2,6-tolylene diisocyanate, benzene diisocyanate, m-xylylene diisocyanate, 1,4-phenylene diisocyanate, 1,3-phenylene diisocyanate, 4,4′-diphenyl diisocyanate, 4,4′-diphenyldimethylmethane diisocyanate, hexamethylene diisocyanate, tolidine diisocyanate, dianisidine diisocyanate, 1,5-naphthalene diisocyanate, 1,4-cyclohexane diisocyanate, or a combination thereof. 26. The method of claim 21, wherein the isocyanate-based reactant comprises a urethane, allophanate, urea, biuret, carbodiimide, uretonimine, isocyanurate, or a combination thereof. 27. The method of claim 21, wherein the isocyanate-based reactant is polymeric diphenylmethane diisocyanate. 28. The method of claim 23, wherein the isocyanate-reactive compound is nucleophilically reactive with an isocyanate. 29. The method of claim 28, wherein the isocyanate-reactive compound is a compound having a hydroxyl group or an amino group capable of reacting with the isocyanate. 30. The method of claim 23, wherein the isocyanate-reactive compound is a polyol. 31. The method of claim 23, wherein the isocyanate-reactive compound is a polyol derived from castor oil, linseed oil, or soy oil. 32. The method of claim 23, wherein the isocyanate-reactive compound is a polyol initiated with a compound selected from the group consisting of glycerol, trimethylopropane, triethanolamine, pentaerythritol, sorbitol sucrose, diamine, tolylene diamine, diaminodiphenylmethane, a polymethylene polyphenylene polyamine, ethanolamine, diethanolamine, or a mixture thereof. 33. The method of claim 23, wherein the isocyanate-reactive compound is a polyester obtained by condensation of a glycol or higher functionality polyol with a dicarboxylic acid; or a hydroxyl terminated polythioether, polyamide, polyesteramide, polycarbonate, polyacetal, polyolefin or polysiloxane. 34. The method of claim 23, wherein the isocyanate-reactive compound is polyoxypropylene glycol, polypropylene oxide-ethylene oxide, propylene glycol, propane diol, glycerin, an amine alkoxylate, or a mixture thereof. 35. The method of claim 23, wherein the isocyanate-reactive compound is polyoxypropylene glycol. 36. The method of claim 21, wherein the mixture in step (a) further comprises a blowing agent or a compound that forms a blowing agent. 37. The method of claim 36, wherein the compound that forms the blowing agent is water. 38. The method of claim 21, wherein the mixture in step (a) further comprises a catalyst that facilitates generation of the foam. 39. The method of claim 38, wherein the catalyst is dibutyltin dilaurate, dibutyltin diacetate, triethylenediamine, 2,2′-dimethylamino diethyl ether, 2-dimethylamino ethanol, stannous octoate, potassium octoate, an alkali metal salt of a carboxylic acid, or a combination thereof. 40. A premix for preparing a polyurethane foam, comprising: (a) a protein containing composition; and(b) an isocyanate-based reactant, wherein the protein containing composition is an isolated, water-soluble polypeptide composition that is capable of stabilizing a polyurethane-based foam, wherein the isolated, water-soluble polypeptide composition comprises one or more of the following features: (a) an amide-I absorption band between about 1633 cm−1 and 1680 cm−1, as determined by solid state FTIR;(b) an amide-II band between approximately 1522 cm−1 and 1560 cm−1, as determined by solid state FTIR;(c) two prominent 1° amide N—H stretch absorption bands centered at about 3200 cm−1, and at about 3300 cm−1, as determined by solid state FTIR;(d) a prominent cluster of protonated nitrogen nuclei defined by 15N chemical shift boundaries at about 94 ppm and at about 100 ppm, and 1H chemical shift boundaries at about 7.6 ppm and at about 8.1 ppm, as determined by solution state, two-dimensional proton-nitrogen coupled NMR;(e) an average molecular weight of between about 600 and about 2,500Daltons;(f) an inability to stabilize an oil-in-water emulsion, wherein, when an aqueous solution comprising 14 parts by weight of protein dissolved or dispersed in 86 parts by weight of water is admixed with 14 parts by weight of PMDI, the aqueous solution and the PMDI produce an unstable suspension that macroscopically phase separates under static conditions within five minutes after mixing;(g) the water-soluble polypeptide composition is capable of stabilizing a polyurethane-based foam relative to a polyurethane-based foam created from the same starting composition lacking the water soluble protein composition; or(h) the water-soluble polypeptide composition is capable of reducing the density of a polyurethane-based foam by at least 5% relative to a polyurethane-based foam created from the same starting composition lacking the water-soluble polypeptide composition;wherein the premix is substantially free of water-insoluble/water dispersible polypeptides. 41. The premix of claim 40, wherein the protein containing composition is an isolated, water-soluble polypeptide composition that is capable of stabilizing a polyurethane-based foam, wherein the isolated, water-soluble polypeptide composition comprises the following features: (a) an amide-I absorption band between about 1633 cm−1 and 1680 cm−1, as determined by solid state FTIR;(b) an amide-II band between approximately 1522 cm−1 and 1560 cm−1, as determined by solid state FTIR;(c) two prominent 1° amide N—H stretch absorption bands centered at about 3200cm−1, and at about 3300 cm−1, as determined by solid state FTIR;(d) a prominent cluster of protonated nitrogen nuclei defined by 15N chemical shift boundaries at about 94 ppm and at about 100 ppm, and 1H chemical shift boundaries at about 7.6 ppm and at about 8.1 ppm, as determined by solution state, two-dimensional proton-nitrogen coupled NMR;(e) an average molecular weight of between about 600 and about 2,500 Daltons;(f) an inability to stabilize an oil-in-water emulsion, wherein, when an aqueous solution comprising 14 parts by weight of protein dissolved or dispersed in 86parts by weight of water is admixed with 14 parts by weight of PMDI, the aqueous solution and the PMDI produce an unstable suspension that macroscopically phase separates under static conditions within five minutes after mixing;(g) the water-soluble polypeptide composition is capable of stabilizing a polyurethane-based foam relative to a polyurethane-based foam created from the same starting composition lacking the water soluble protein composition; and(h) the water-soluble polypeptide composition is capable of reducing the density of a polyurethane-based foam by at least 5% relative to a polyurethane-based foam created from the same starting composition lacking the water-soluble polypeptide composition. 42. The premix of claim 40, wherein the isocyanate-based reactant is an organic polyisocyanate. 43. An article comprising the foam of claim 1. 44. The polyurethane foam of claim 1, wherein the isolated, water-soluble polypeptide composition has at least the following features: (a) an amide-I absorption band between about 1633 cm−1 and 1680 cm−1, as determined by solid state FTIR;(b) an amide-II band between approximately 1522 cm−1 and 1560 cm−1, as determined by solid state FTIR;(c) two prominent 1° amide N—H stretch absorption bands centered at about 3200 cm−1, and at about 3300 cm1, as determined by solid state FTIR;(d) a prominent cluster of protonated nitrogen nuclei defined by 15N chemical shift boundaries at about 94 ppm and at about 100 ppm, and 1H chemical shift boundaries at about 7.6 ppm and at about 8.1 ppm, as determined by solution state, two-dimensional proton-nitrogen coupled NMR;(e) an average molecular weight of between about 600 and about 2,500 Daltons; and(f) an inability to stabilize an oil-in-water emulsion, wherein, when an aqueous solution comprising 14 parts by weight of protein dissolved or dispersed in 86 parts by weight of water is admixed with 14 parts by weight of PMDI, the aqueous solution and the PMDI produce an unstable suspension that macroscopically phase separates under static conditions within five minutes after mixing. 45. A polyurethane foam comprising a reaction product of a mixture comprising: (a) an isocyanate-based reactant;(b) an isocyanate-reactive compound; and(c) an isolated, water-soluble polypeptide composition that is capable of stabilizing a polyurethane-based foam, wherein the composition comprises one or more of the following features: (a) an amide-I absorption band between about 1633 cm−1 and 1680 cm−1, as determined by solid state FTIR;(b) an amide-II band between approximately 1522 cm−1 and 1560 cm−1, as determined by solid state FTIR;(c) two prominent 1° amide N—H stretch absorption bands centered at about 3200 cm−1, and at about 3300 cm−1, as determined by solid state FTIR;(d) a prominent cluster of protonated nitrogen nuclei defined by 15N chemical shift boundaries at about 94 ppm and at about 100 ppm, and 1H chemical shift boundaries at about 7.6 ppm and at about 8.1 ppm, as determined by solution state, two-dimensional proton-nitrogen coupled NMR;(e) an average molecular weight of between about 600 and about 2,500 Daltons;(f) an inability to stabilize an oil-in-water emulsion, wherein, when an aqueous solution comprising 14 parts by weight of protein dissolved or dispersed in 86 parts by weight of water is admixed with 14 parts by weight of PMDI, the aqueous solution and the PMDI produce an unstable suspension that macroscopically phase separates under static conditions within five minutes after mixing;(g) the water-soluble polypeptide composition is capable of stabilizing a polyurethane-based foam relative to a polyurethane-based foam created from the same starting composition lacking the water soluble protein composition; or(h) the water-soluble polypeptide composition is capable of reducing the density of a polyurethane-based foam by at least 5% relative to a polyurethane-based foam created from the same starting composition lacking the water-soluble polypeptide composition;wherein the foam is substantially free of water-insoluble/water dispersible polypeptides. 46. The polyurethane foam of claim 45, wherein the isocyanate-based reactant is an organic polyisocyanate. 47. The polyurethane foam of claim 46, wherein the organic polyisocyanate is polymeric diphenylmethane diisocyanate, 2,4-tolylene diisocyanate, 2,6-tolylene diisocyanate, benzene diisocyanate, m-xylylene diisocyanate, 1,4-phenylene diisocyanate,1,3-phenylene diisocyanate, 4,4′-diphenyl diisocyanate, 4,4′-diphenyldimethylmethane diisocyanate, hexamethylene diisocyanate, tolidine diisocyanate, dianisidine diisocyanate, 1,5-naphthalene diisocyanate, 1,4-cyclohexane diisocyanate, or a combination thereof. 48. The polyurethane foam of claim 45, wherein the isocyanate-based reactant comprises a urethane, allophanate, urea, biuret, carbodiimide, uretonimine, isocyanurate, or a combination thereof. 49. The polyurethane foam of claim 45, wherein the isocyanate-based reactant is polymeric diphenylmethane diisocyanate. 50. The polyurethane foam of claim 49, wherein the isocyanate-reactive compound is a compound having a hydroxyl group or an amino group capable of reacting with the isocyanate. 51. The polyurethane foam of claim 49, wherein the isocyanate-reactive compound is a polyol. 52. The polyurethane foam of claim 45, wherein the foam has a density in the range of from about 0.01 g/cm3 to about 0.5 g/cm3 as determined by ASTM D-7487. 53. The polyurethane foam of claim 45, wherein the foam has a density that is from 5% to 80% less dense than a foam created from the same starting composition lacking the protein containing composition.
연구과제 타임라인
LOADING...
LOADING...
LOADING...
LOADING...
LOADING...
이 특허에 인용된 특허 (63)
R. Christopher Clark ; Brian L. Hilker, Additives for enhanced hydrocarbon compatibility in rigid polyurethane foam systems.
Gruber Norma J. (Worthington OH) Powell Clois E. (Westerville OH), Aqueous hydroxyl-acrylic latex and water dispersible multi-isocyanate adhesive composition.
Espiard, Philippe; Mahieuxe, Bruno, Insulation product in particular thermal containing a binder based on phenol-formaldehyde resin and method for making same.
Peterson Brian H. ; Rossitto Frank C. ; Nicola ; Jr. William J. ; Blue Clarence D., Isocyanate-terminated prepolymers and rigid-foams produced therefrom.
Krinski Thomas L. (Granite City IL) Coco Charles E. (St. Louis MO) Steinmetz Alan L. (West Bloomfield MI), Modified protein adhesive binder and process for producing using cationic monomers.
Cioca George (Coatesville PA) Feeley George F. (Downington PA) Brabson Joseph B. (Wilmington DE) Barth Peter (Neuwied DEX), Moisture vapor permeable sheet materials.
Reischl Artur (Leverkusen DEX) Wagner Kuno (Leverkusen DEX), Process for the production of polyurethane plastics in which polyisocyanates are reacted with reactive organic fillers c.
Nakos, Panagiotis; Athanassiadou, Eleftheria; Coutinho, Joao Manuel Aires, Production of high added value products from resin-bonded waste composite wood products.
Gibson Paul W. (Mt. Zion IL) Orthoefer Frank T. (Decatur IL), Proteinaceous foaming compositions and method for preparing foamed proteinaceous products.
Thames,Shelby F.; Sankovich,Boris G.; Shera,Jeanne N.; Thompson,Robert B.; Mendon,Sharathkumar K.; Evans,James M., Soy protein based adhesive and particleboard.
Kuo Monlin ; Myers Deland J. ; Heemstra Howard ; Curry Daniel ; Adams Daniel O. ; Stokke Douglas D., Soybean-based adhesive resins and composite products utilizing such adhesives.
Kuo, Monlin; Myers, Deland J.; Heemstra, Howard; Curry, Daniel; Adams, Daniel O.; Stokke, Douglas D., Soybean-based adhesive resins and composite products utilizing such adhesives.
Kintzley, Tom G.; Helkey, John; Holte, Ivan; Johnson, Lee Roy; Miller, Todd R., Wood composites, methods of production, and methods of manufacture thereof.
※ AI-Helper는 부적절한 답변을 할 수 있습니다.