IP Library Granted Patent US 9,353,208
Granted Patent B2
US 9,353,208 · App. 14/259,884 · Granted May 31, 2016

Method for preparing a sol-gel resin

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Quick Facts
Patent No.
US 9,353,208
App. No.
14/259,884
Granted
May 31, 2016
Kind
B2
Abstract

Sol-gel resins can be prepared using one or two-step processes to produce small granules or pellets of resin that are easy to handle. The methods include agitating phenolic compounds and aldehydes in the presence of a catalyst and a solvent. The reactants are brought together over a period of time to avoid an undesirable buildup of heat within the reaction mass. Condensation of the material continues under agitation sufficient to knead the material as it gels. During this gelation, the material begins to form into smaller parts until particles, the shape of granules, are produced. The condensation continues to the degree that the material is no longer capable of sintering during packaging and storage. The material thus made can be easily discharged, packaged, portioned, and further processed.

Claims (34)

1. A method for preparing a sol-gel resin comprising:

introducing a hydroxylated benzene and optionally a catalyst into a reactor;

introducing an aldehyde into the reactor with agitation to form a reaction mixture;

reacting the reaction mixture for a period of time sufficient to consume a portion of the hydroxylated benzene to form a liquid resin precursor;

transferring the liquid resin precursor from the reactor into a mixer; and

agitating the liquid resin precursor in the mixer for a period of time sufficient to form the sol-gel resin in a particulate form.

2. The method of claim 1 wherein the reactor is configured to control the temperature of material therein.

3. The method of claim 1 wherein the aldehyde is introduced into the reactor over a period of time sufficient to control a reaction exotherm.

4. The method of claim 3 wherein the reaction exotherm is controlled for the period of time sufficient to consume more than above about 70% of the hydroxylated benzene.

5. The method of claim 3 wherein the reaction exotherm is controlled for the period of time sufficient to consume from about 30% to about 90% of the aldehyde.

6. The method of claim 1 wherein the resin precursor is agitated in the mixer at a temperature maintained between about 25° C. to about 120° C.

7. The method of claim 6 wherein the temperature is maintained between about 40° C. to about 80° C.

8. The method of claim 1 wherein the molar ratio of hydroxylated benzene to aldehyde is about 0.20 to about 0.75.

9. The method of claim 1 wherein the resin precursor is agitated within the mixer under conditions sufficient to produce the sol-gel resin having an average particle size of from about 0.5 mm to about 20 mm.

10. The method of claim 1 further comprising shaping the sol-gel resin into a desired geometry that does not sinter or agglomerate.

11. The method of claim 10 wherein the shaped sol-gel resin is cured at a temperature of from about 50° C. to about 100° C.

12. The method of claim 1 free of a step to isolate the sol-gel resin from a suspending liquid reaction media.

13. The method of claim 1 free of reaction phases that are immiscible or insoluble with each other.

14. A method for preparing a sol-gel resin comprising:

introducing a hydroxylated benzene and optionally a catalyst into a mixer;

introducing an aldehyde into the mixer with agitation to form a reaction mixture; and

agitating the reaction mixture for a period of time sufficient to form the sol-gel resin in a particulate form.

15. The method of claim 14 wherein the mixer is configured to control the temperature of material therein.

16. The method of claim 14 wherein the aldehyde is introduced into the mixer over a period of time sufficient to control a reaction exotherm.

17. The method of claim 16 wherein the reaction exotherm is controlled for the period of time sufficient to consume more than above about 70% of the hydroxylated benzene.

18. The method of claim 16 wherein the reaction exotherm is controlled for period of time sufficient to consume from about 30% to about 90% of the aldehyde.

19. The method of claim 14 wherein the resin precursor is agitated in the mixer at a temperature maintained between about 25° C. to about 120° C.

20. The method of claim 19 wherein the temperature is maintained between about 40° C. to about 80° C.

21. The method of claim 14 wherein a molar ratio of hydroxylated benzene to aldehyde is about 0.20 to about 0.75.

22. The method of claim 14 wherein the resin precursor is agitated within the mixer under conditions sufficient to produce the sol-gel resin having an average particle size of from about 0.5 mm to about 20 mm.

23. The method of claim 14 further comprising shaping the sol-gel resin into a desired geometry that does not sinter or agglomerate.

24. The method of claim 23 wherein the shaped sol-gel resin is cured at a temperature of from about 50° C. to about 100° C.

25. The method of claim 1 free of a step to isolate the sol-gel resin from a suspending liquid reaction media.

26. The method of claim 14 free of reaction phases that are immiscible or insoluble with each other.

Assignments (22)
SECURITY INTEREST Recorded May 12, 2025
From: BAKELITE CHEMICALS LLC; BAKELITE UK HOLDING LTD.; BAKELITE GMBH; BAKELITE SYNTHETICS UK
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 071090/0740 →
ASSIGNMENT OF PATENT AND TRADEMARK SECURITY INTEREST Recorded May 12, 2025
From: MACQUARIE CAPITAL FUNDING LLC
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 071276/0379 →
SECURITY INTEREST Recorded Jan 23, 2025
From: BAKELITE CHEMICALS LLC; BAKELITE UK HOLDING LTD.; BAKELITE GMBH; BAKELITE SYNTHETICS UK LIMITED
To: GOLDMAN SACHS BANK USA
Reel/Frame 069981/0468 →
RELEASE OF SECURITY INTEREST Recorded Jun 15, 2022
From: GOLDMAN SACHS SPECIALTY LENDING GROUP, L.P.
To: HEXION VAD LLC
Reel/Frame 060209/0558 →
SECURITY INTEREST Recorded Jun 9, 2022
From: GEORGIA-PACIFIC CHEMICALS LLC; GEORGIA-PACIFIC CONSUMER PRODUCTS LP; ENERG2 TECHNOLOGIES, INC.; KOCH AGRONOMIC SERVICES LLC; BAKELITE UK HOLDING LTD.; SURFACE TECH LLC
To: GOLDMAN SACHS BANK USA, AS ADMINISTRATIVE AGENT
Reel/Frame 060328/0250 →
SECURITY INTEREST Recorded Jun 9, 2022
From: GEORGIA-PACIFIC CHEMICALS LLC; GEORGIA-PACIFIC CONSUMER PRODUCTS LP; ENERG2 TECHNOLOGIES, INC.; KOCH AGRONOMIC SERVICES LLC; BAKELITE UK HOLDING LTD.
To: MACQUARIE CAPITAL FUNDING LLC, AS ADMINISTRATIVE AGENT
Reel/Frame 060328/0327 →
CHANGE OF NAME Recorded May 3, 2022
From: HEXION VAD LLC
To: BAKELITE LLC
Reel/Frame 059926/0973 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 3, 2022
From: BAKELITE LLC
To: BAKELITE UK HOLDING LTD.
Reel/Frame 060377/0699 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 30, 2021
From: HEXION INC.
To: HEXION VAD LLC
Reel/Frame 057323/0086 →
RELEASE OF SECURITY INTEREST Recorded May 12, 2021
From: JPMORGAN CHASE BANK, N.A.
To: HEXION INC.
Reel/Frame 056219/0582 →
RELEASE OF SECURITY INTEREST Recorded May 12, 2021
From: JPMORGAN CHASE BANK, N.A.
To: HEXION INC.
Reel/Frame 056219/0677 →
SECURITY INTEREST Recorded May 5, 2021
From: HEXION VAD LLC
To: GOLDMAN SACHS SPECIALTY LENDING GROUP, L.P., AS COLLATERAL AGENT
Reel/Frame 056145/0957 →
PATENT SECURITY INTEREST (ABL) Recorded Jul 12, 2019
From: HEXION INC.
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 049740/0770 →
PATENT SECURITY INTEREST (TERM LOAN) Recorded Jul 12, 2019
From: HEXION INC.
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 049741/0425 →
PATENT SECURITY INTEREST ASSIGNMENT AGREEMENT Recorded Apr 3, 2019
From: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS THE PRIOR COLLATERAL AGENT
To: WILMINGTON SAVINGS FUND SOCIETY, FSB, AS THE CURRENT COLLATERAL AGENT
Reel/Frame 048788/0617 →
RELEASE OF SECURITY INTEREST Recorded Feb 23, 2017
From: WILMINGTON TRUST, NATIONAL ASSOCIATION
To: HEXION INC. (FORMERLY KNOWN AS MOMENTIVE SPECIALTY CHEMICALS INC.)
Reel/Frame 041793/0754 →
SECURITY INTEREST Recorded Feb 13, 2017
From: HEXION INC.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 041693/0888 →
SECURITY INTEREST Recorded Feb 16, 2015
From: MOMENTIVE SPECIALTY CHEMICALS INC.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 034967/0872 →
CHANGE OF NAME Recorded Feb 3, 2015
From: MOMENTIVE SPECIALTY CHEMICALS INC.
To: HEXION INC.
Reel/Frame 034882/0280 →
SECURITY INTEREST Recorded Aug 21, 2014
From: MOMENTIVE SPECIALTY CHEMICALS INC.
To: WILMINGTON TRUST COMPANY, AS COLLATERAL AGENT
Reel/Frame 033579/0689 →
SECURITY INTEREST Recorded Aug 20, 2014
From: MOMENTIVE SPECIALTY CHEMICALS INC.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 033577/0542 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 16, 2014
From: ARBUCKLE, STEPHEN W.; BADINI, GABRIELE; HUGGINS, JOHN; GANGAL, SANJAY
To: MOMENTIVE SPECIALTY CHEMICALS INC.
Reel/Frame 033110/0226 →