POLYMER DERIVATIVES AND COMPOSITES FROM THE DISSOLUTION OF LIGNOCELLULOSICS IN IONIC LIQUIDS

• US 20080188636A1
• Filed: 02/06/2008
• Published: 08/07/2008
• Est. Priority Date: 02/06/2007
• Status: Abandoned Application

• Current Assignee: North Carolina State University (University of North Carolina System)
• Original Assignee: North Carolina State University (University of North Carolina System)
• Inventors: Argyropoulos, Dimitris, Xie, Haibo
• Application Number:
  US12/026,998
• Publication Number:
  US 20080188636A1
• Time in Patent Office: Days
• US Class Current: 527/300
• CPC Class Codes: C08H 8/00 Macromolecular compounds derived from lignocellulosic materials pretreatment thereof B27N
• CPC Class Codes: C08L 2666/04 Macromolecular compounds according to groups C08L7/00 - C08L49/00, or C08L55/00 - C08L57/00; Derivatives thereof
• CPC Class Codes: C08L 2666/14 Macromolecular compounds according to C08L59/00 - C08L87/00; Derivatives thereof
• CPC Class Codes: C08L 2666/26 Natural polymers, natural resins or derivatives thereof according to C08L1/00 - C08L5/00, C08L89/00, C08L93/00, C08L97/00 or C08L99/00
• CPC Class Codes: C08L 29/04 Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids
• CPC Class Codes: C08L 33/20 Homopolymers or copolymers of acrylonitrile C08L55/02 takes precedence
• CPC Class Codes: C08L 71/02 Polyalkylene oxides
• CPC Class Codes: C08L 97/005 Lignin
• CPC Class Codes: C08L 97/02 Lignocellulosic material, e.g. wood, straw or bagasse manufacture of articles made from lignocellulosic material by dry processes B27N

Abstract

The present invention provides wood derivatives and composite materials prepared by first solvating a lignocellulosic material using an ionic liquid. The solvated lignocellulosic material can be derivatized to incorporate functional groups, particularly groups that facilitate later combination with polymer materials, including non-polymer polymers. The polymeric materials can be combined with the derivatized lignocellulosic material in solution, or the derivatized lignocellulosic material can be isolated and later combined with the polymeric material in a melt. The invention encompasses a variety of wood derivatives, composites, and nanocomposites useful for preparing multiple types of products, including membranes, fibers, and formed parts.

Claims

1. A composite material comprising an ionic liquid solvated lignocellulosic material in combination with a further polymeric component.

2. The composite material according to claim 1, wherein the further polymeric component comprises a natural polymer.

3. The composite material according to claim 1, wherein the further polymeric component comprises a synthetic polymer.

4. The composite material according to claim 1, wherein the further polymeric component comprises a non-polar polymer.

5. The composite material according to claim 1, wherein the further polymeric component is selected from the group consisting of polysaccharides, polyesters, polyamides, aromatic polyamides, polyimides, polyurethanes, polysiloxanes, aromatic polymers, phenol polymers, polysulfides, polyacetals, polyolefins, halogenated polyolefins, polyethylene oxides, polyacrylates, polymethacrylates, polycarbonates, polydienes, and combinations thereof.

6. The composite material according to claim 1, wherein the solvated lignocellulosic material is a derivatized material.

7. The composite material according to claim 6, wherein the solvated lignocellulosic material is chemically derivatized through a reaction with one or more naturally occurring hydroxyl moiety present in the lignocellulosic material to add a different, derivatizing chemical moiety.

8. The composite material according to claim 7, wherein the derivatizing moiety comprises a carboxyl group that reacts with the hydroxyl moiety on the lignocellulosic material to form an ester linkage.

9. The composite material according to claim 7, wherein the derivatizing moiety comprises a halogen leaving group that reacts with the hydroxyl moiety on the lignocellulosic material to form an ether linkage.

10. The composite material according to claim 7, wherein the derivatizing moiety is selected from the group consisting of carboxylic acids, carboxylic esters, acyl halides, acyl pseudohalides, acid anhydrides, aldehydes, ketones, carboxamides, aliphatic halides, and combinations thereof.

11. The composite material according to claim 1, wherein the composite material is in the form of a liquid melt.

12. The composite material according to claim 1, wherein the composite material is in the form of a fiber or membrane.

13. The composite material according to claim 1, wherein the ionic liquid solvated lignocellulosic material comprises a wood.

14. A derivatized lignocellulosic material, comprising a lignocellulosic material that has been chemically derivatized such that one or more naturally occurring hydroxyl moiety present in the lignocellulosic material has been replaced with a different, derivatizing chemical moiety.

15. The derivatized lignocellulosic material according to claim 14, wherein the lignocellulosic material comprises an ionic liquid solvated lignocellulosic material.

16. The derivatized lignocellulosic material according to claim 14, wherein the lignocellulosic material comprises a wood.

17. The derivatized lignocellulosic material according to claim 14, wherein the derivatizing moiety comprises a carboxyl group that reacts with the hydroxyl moiety on the lignocellulosic material such that the derivatizing moiety is linked to the lignocellulosic material via an ester linkage.

18. The derivatized lignocellulosic material according to claim 14, wherein the derivatizing moiety comprises a halogen leaving group that reacts with the hydroxyl moiety on the lignocellulosic material such that the derivatizing moiety is linked to the lignocellulosic material via an ether linkage.

19. The derivatized lignocellulosic material according to claim 14, wherein the derivatizing moiety is selected from the group consisting of carboxylic acids, carboxylic esters, acyl halides, acyl pseudohalides, acid anhydrides, aldehydes, ketones, carboxamides, aliphatic halides, and combinations thereof.

20. The derivatized lignocellulosic material according to claim 14, wherein the derivatized lignocellulosic material is solubilized in an ionic liquid.

21. The derivatized lignocellulosic material according to claim 14, wherein the derivatized lignocellulosic material is a solid.

22. The derivatized lignocellulosic material according to claim 21, wherein the derivatized lignocellulosic material is a powder.

23. A method of preparing a composite material comprising dissolving a lignocellulosic material in an ionic liquid to form a solution and combining the solvated lignocellulosic material with a further polymeric component.

24. The method according to claim 23, wherein the further polymeric component comprises a natural polymer.

25. The method according to claim 23, wherein the further polymeric component comprises a synthetic polymer.

26. The method according to claim 25, wherein the further polymeric component comprises a non-polar polymer.

27. The method according to claim 25, wherein the further polymeric component is selected from the group consisting of polysaccharides, polyesters, polyamides, aromatic polyamides, polyimides, polyurethanes, polysiloxanes, aromatic polymers, phenol polymers, polysulfides, polyacetals, polyolefins, halogenated polyolefins, polyethylene oxides, polyacrylates, polymethacrylates, polycarbonates, polydienes, and combinations thereof.

28. The method according to claim 23, further comprising, prior to said combining step, derivatizing the solvated lignocellulosic material.

29. The method according to claim 28, wherein said derivatizing step comprises combining the solvated lignocellulosic material with a derivatizing chemical moiety to replace one or more naturally occurring hydroxyl moiety present in the lignocellulosic material with the different, derivatizing moiety.

30. The method according to claim 29, wherein the derivatizing moiety comprises a carboxyl group that reacts with the hydroxyl moiety on the lignocellulosic material to form an ester linkage.

31. The method according to claim 29, wherein the derivatizing moiety comprises a halogen leaving group that reacts with the hydroxyl moiety on the lignocellulosic material to form an ether linkage.

32. The method according to claim 29, wherein the derivatizing moiety is selected from the group consisting of carboxylic acids, carboxylic esters, acyl halides, acyl pseudohalides, acid anhydrides, aldehydes, ketones, carboxamides, aliphatic halides, and combinations thereof.

33. The method according to claim 23, wherein said combining step comprises melt processing or solution blending the solvated lignocellulosic material and the further polymeric component.

34. The method according to claim 23, wherein said combining step comprises adding the further polymeric component to the solution.

35. The method according to claim 23, further comprising, prior to said combining step, regenerating the solvated lignocellulosic material to form a solid, regenerated lignocellulosic material.

36. The method according to claim 35, wherein said combining step comprises mixing the regenerated lignocellulosic material with the further polymeric component to form a melt.

37. The method according to claim 36, further comprising extruding the melt to form composite fibers.

38. The method according to claim 36, further comprising molding to the melt to a desired form.

39. The method according to claim 23, wherein the ionic liquid comprises a material formed of a cation and an anion, wherein the cation is selected from the group consisting of imidazoles, pyrazoles, thiazoles, isothiazoles, azathiozoles, oxothiazoles, oxazines, oxazolines, oxazaboroles, dithiozoles, triazoles, delenozoles, oxaphospholes, pyrroles, boroles, furans, thiophenes, phospholes, pentazoles, indoles, indolines, oxazoles, isoxazoles, isotetrazoles, tetrazoles, benzofurans, dibenzofurans, benzothiophenes, dibenzothiophenes, thiadiazoles, pyridines, pyrimidines, pyrazines, pyridazines, piperazines, piperidines, morpholones, pyrans, annolines, phthalazines, quinazolines, guanidiniums, quinxalines, choline-based analogues, derivatives thereof, and combinations thereof, and wherein the anion is selected from the group consisting of halogens, phosphates, alkylphosphates, alkenylphosphates, BF₄⁻

, PF₆⁻

, AsF₆⁻

, NO₃⁻

, N(CN)₂⁻

, N(SO₃CF₃)₂⁻

, amino acids, substituted or unsubstituted carboranes, perchlorates, pseudohalogens, metal chloride-based Lewis acids, C_1-6 carboxylates, and combinations thereof.

40. The method according to claim 39, wherein the cation is selected from the group consisting of imidazoles and pyridines, and the anion is selected from the group consisting of halogens, phosphates, alkylphosphates, alkenylphosphates, and bis(trifluoromethylsulfonyl)imide.

41. The method according to claim 23, wherein the lignocellulosic material is selected from the group consisting of tobacco, corn, corn stovers, corn residues, cornhusks, sugarcane bagasse, castor oil plant, rapeseed plant, soybean plant, cereal straw, grain processing by-products, bamboo, bamboo pulp, bamboo sawdust, energy grasses, rice straw, paper sludge, waste papers, recycled paper, recycled pulp, and combinations thereof.

42. The method according to claim 41, wherein the lignocellulosic material is a wood.

43. The method according to claim 23, wherein the lignocellulosic material, prior to dissolving in the ionic liquid, is in a form selected from the group consisting of ball-milled wood powder, sawdust, thermomechanical pulp fibers, wood chips, and combinations thereof.

44. A method of preparing a derivatized lignocellulosic material comprising dissolving a lignocellulosic material in an ionic liquid to form a solution and combining the solvated lignocellulosic material with a derivatizing chemical moiety to replace one or more naturally occurring hydroxyl moiety present in the lignocellulosic material with the different, derivatizing moiety.

45. The method according to claim 44, wherein the derivatizing moiety comprises a carboxyl group that reacts with the hydroxyl moiety on the lignocellulosic material to form an ester linkage.

46. The method according to claim 44, wherein the derivatizing moiety comprises a halogen leaving group that reacts with the hydroxyl moiety on the lignocellulosic material to form an ether linkage.

47. The method according to claim 44, wherein the derivatizing moiety is selected from the group consisting of carboxylic acids, carboxylic esters, acyl halides, acyl pseudohalides, acid anhydrides, aldehydes, ketones, carboxamides, aliphatic halides, and combinations thereof.

48. The method according to claim 44, further comprising regenerating the derivatized lignocellulosic material to form a solid, regenerated derivatized lignocellulosic material.

49. The method according to claim 44, wherein the ionic liquid comprises a material formed of a cation and an anion, wherein the cation is selected from the group consisting of imidazoles, pyrazoles, thiazoles, isothiazoles, azathiozoles, oxothiazoles, oxazines, oxazolines, oxazaboroles, dithiozoles, triazoles, delenozoles, oxaphospholes, pyrroles, boroles, furans, thiophenes, phospholes, pentazoles, indoles, indolines, oxazoles, isoxazoles, isotetrazoles, tetrazoles, benzofurans, dibenzofurans, benzothiophenes, dibenzothiophenes, thiadiazoles, pyridines, pyrimidines, pyrazines, pyridazines, piperazines, piperidines, morpholones, pyrans, annolines, phthalazines, quinazolines, guanidiniums, quinxalines, choline-based analogues, derivatives thereof, and combinations thereof, and wherein the anion is selected from the group consisting of halogens, phosphates, alkylphosphates, alkenylphosphates, BF₄⁻

, PF₆⁻

, AsF₆⁻

, NO₃⁻

, N(CN)₂⁻

, N(SO₃CF₃)₂⁻

, amino acids, substituted or unsubstituted carboranes, perchlorates, pseudohalogens, metal chloride-based Lewis acids, C_1-6 carboxylates, and combinations thereof.

50. The method according to claim 49, wherein the cation is selected from the group consisting of imidazoles and pyridines, and the anion is selected from the group consisting of halogens, phosphates, alkylphosphates, alkenylphosphates, and bis(trifluoromethylsulfonyl)imide.

51. The method according to claim 44, wherein the lignocellulosic material is selected from the group consisting of tobacco, corn, corn stovers, corn residues, cornhusks, sugarcane bagasse, castor oil plant, rapeseed plant, soybean plant, cereal straw, grain processing by-products, bamboo, bamboo pulp, bamboo sawdust, energy grasses, wood, and combinations thereof.

52. The method according to claim 51, wherein the lignocellulosic material is a wood.

53. The method according to claim 44, wherein the lignocellulosic material, prior to dissolving in the ionic liquid, is in a form selected from the group consisting of ball-milled wood powder, sawdust, thermomechanical pulp fibers, wood chips, and combinations thereof.