IP Library Granted Patent US 8,436,061
Granted Patent B2
US 8,436,061 · App. 13/218,415 · Granted May 7, 2013

Organic, open cell foam materials, their carbonized derivatives, and methods for producing same

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,436,061
App. No.
13/218,415
Granted
May 7, 2013
Kind
B2
Abstract

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.

Claims (55)

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.

Assignments (9)
RELEASE OF SECURITY INTEREST Recorded Oct 16, 2024
From: COMERICA BANK
To: AMERICAN AEROGEL CORPORATION
Reel/Frame 068911/0467 →
RELEASE OF SECURITY INTEREST Recorded Aug 11, 2020
From: SUSTAINABLE GROWTH FUND S.C.SP SICAV-SIF
To: AMERICAN AEROGEL CORPORATION
Reel/Frame 053459/0573 →
SECURITY INTEREST Recorded Aug 7, 2020
From: AMERICAN AEROGEL CORPORATION
To: ESCALATE CAPITAL IV, LP
Reel/Frame 053434/0235 →
SECURITY INTEREST Recorded Jan 6, 2020
From: AMERICAN AEROGEL CORPORATION
To: COMERICA BANK
Reel/Frame 051429/0515 →
CORRECTIVE ASSIGNMENT TO CORRECT THE RECEIVING PARTY DATA PREVIOUSLY RECORDED ON REEL 047611 FRAME 0824. ASSIGNOR(S) HEREBY CONFIRMS THE CORRECTING TYPO IN NAME OF RECEIVING PARTY. Recorded Nov 29, 2018
From: AMERICAN AEROGEL CORPORATION
To: SUSTAINABLE GROWTH FUND, SCSP, SICAV-SIF
Reel/Frame 047687/0056 →
SECURITY INTEREST Recorded Nov 28, 2018
From: AMERICAN AEROGEL CORPORATION
To: SUSTAINABLE GROTH FUND, SCSP, SICAV-SIF
Reel/Frame 047611/0824 →
RELEASE OF SECURITY INTEREST Recorded Oct 24, 2017
From: BAMCG BRIDGE PARTNERS LP
To: AMERICAN AEROGEL CORPORATION
Reel/Frame 044281/0411 →
SECURITY INTEREST Recorded Jul 31, 2017
From: AMERICAN AEROGEL CORPORATION
To: BAMCG BRIDGE PARTNERS LP
Reel/Frame 043140/0754 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 7, 2011
From: ALBERT, DONALD F.; ANDREWS, GREG R.; BRUNO, JOSEPH W.
To: AMERICAN AEROGEL CORPORATION
Reel/Frame 026869/0057 →