Organic, open cell foam materials, their carbonized derivatives, and methods for producing same
View Patent ↗Organic, small pore area materials (“SPMs”) are provided comprising open cell foams in unlimited sizes and shapes. These SPMs exhibit minimal shrinkage and cracking. Processes for preparing SPMs are also provided that do not require supercritical extraction. These processes comprise sol-gel polymerization of a hydroxylated aromatic in the presence of at least one suitable electrophilic linking agent and at least one suitable solvent capable of strengthening the sol-gel. Also disclosed are the carbonized derivatives of the organic SPMs.
1. A method for removing fluid from a so get comprising the steps of:
(a) forming, a solution;
(b) allowing the solution of step (a) to form a sol-gel;
(c) adding a low surface tension solvent to one side of the sol-gel of step (b);
(d) applying a pressure differential across the sol-gel of step (c);
(e) removing substantially all of the original pore fluid portion of the sol-gel of step (d); and
(f) removing the low surface tension solvent.
2. A method for preparing an organic, low density microcellular material, said method comprising the steps of:
(a) forming a solution;
(b) allowing the solution of step (a) to form a sol-gel;
(c) adding a low surface tension solvent to one side of the sol-gel of step (b);
(d) applying a pressure differential across the sol-gel of step (c);
(e) removing substantially all of the original pore fluid portion of the sol-gel of step (d); and
(f) removing the low surface tension solvent.
3. A method for preparing art organic, low density microcellular material, said method comprising the steps of:
(a) forming a solution comprising a hydroxylated aromatic, an electrophilic linking agent, and a hydrogen-bonding agent
(b) allowing the solution of step (a) to form a sol-gel;
(c) adding a low surface tension solvent to one side of the sol-gel of step (b);
(d) applying a pressure differential across the so gel of step (c);
(e) removing substantially all of the original pore fluid portion of the sol-gel of step (d); and
(f) removing the low surface tension solvent.
4. A method for preparing an organic, small pore area material, said method comprising the steps of:
(a) forming a solution;
(b) allowing the solution of step (a) to form a sol-gel;
(c) adding a low surface tension solvent to one side of the sol-gel of step (b);
(d) applying a pressure differential across the sol-gel of step (c);
(e) removing substantially all of the original pore fluid portion of the sol-gel of step (d); and
(f) removing the low surface tension solvent.
5. A method for preparing an organic, small pore area material, said method comprising the steps of:
(a) forming a solution comprising a hydroxylated aromatic, an electrophilic linking agent, and a hydrogen-bonding agent;
(b) allowing the solution of step (a) to form a sol-gel;
(c) adding a low surface tension solvent to one side of the sol-gel;
(d) applying a pressure differential across the sol-gel of step (c);
(e) removing substantially all of the original pore fluid portion of the sol-gel of step (d); and
(f) removing the low surface tension solvent.
6. The method according to anyone of claims 1 - 5 , wherein said low surface tension solvent is an organic solvent with a surface tension lower than that of the solvent used in preparing the sol-gel.
7. The method according to anyone of claims 1 - 5 , wherein said low surface tension solvent is selected from the group consisting of hexane, ethyl ether, pentane: isopentane, acetone, methanol, ethanol and isopropanol.
8. The method according to anyone of claims 1 - 5 , wherein said low surface tension solvent comprises a hexane compound.
9. The method of claim 3 or 5 , wherein said hydroxylated aromatic comprises a hydroxylated benzene compound.
10. The method of claim 3 or 5 , wherein said hydroxylated aromatic comprises a phenolic novolak compound.
11. The method of any one of claims 1 - 5 , wherein said low surface tension solvent is removed by evaporation, freeze drying, or centrifugation.
12. The method of claim 3 or 5 , wherein said electrophilic linking agent comprises an aldehyde.
13. The method of claim 3 or 5 , wherein said electrophilic linking agent comprises furfural.
14. The method of claim 3 or 5 , wherein said hydrogen-bonding agent comprises a carboxylic acid.
15. The method of claim 3 or 5 , wherein said hydrogen-bonding agent comprises acetic acid, formic acid, propionic acid, butyric acid, pentanoic acid or an isomer thereof.
16. The method of claim 3 or 5 , wherein said hydrogen-bonding agent comprises acetic acid.
17. The method of any one of claims 2 - 5 , further comprising the step (g) of pyrolizing said material at a pyrolysis temperature to form a carbonized derivative of said material.
18. The method of claim 3 or 5 , wherein said electrophilic linking agent comprises alcohol.
19. The method of claim 3 or 5 , wherein said alcohol is furfuryl alcohol.
20. The method of claim 3 or 5 , wherein the solution formed in step (a) further comprises a catalyzing agent.
21. The method of claim 20 , wherein said catalyzing agent is independently selected from the group consisting of hydrochloric acid, sulfuric acid and hydrobromic acid.
22. The method of claim 3 or 5 , wherein the solution formed in step (a) further comprises a surfactant.
23. The method of any one of claims 1 - 5 , wherein step (b) includes the substep of subjecting said solution to either: (i) a temperature or a pressure higher than ambient; or (ii) a temperature and a pressure higher than ambient.
24. The method of any one of claims 1 - 5 , wherein step (d) comprises applying a vas pressure to one side of the sol-gel with the other side exposed to atmospheric pressure.
25. The method of any one of claims 1 - 5 , wherein step (d) comprises applying a reduced pressure to one side of the sol-gel with the other side exposed to atmospheric pressure.