IP Library Granted Patent US 12,305,143
Granted Patent B2
US 12,305,143 · App. 17/608,733 · Granted May 20, 2025

Using silica-zirconia catalysts in processes to reduce glycidol, glycidyl esters, or both glycidol and glycidyl esters

Inventors: Demetrius Michos (Clarksville, MD); Chelsea L. Grimes (Stoney Beach, MD); Cristian Libanati (Silver Spring, MD); Ignazio Catucci (Busto Garolfo, IT)
Assignee: W.R. GRACE & CO.-CONN.
C11B3/02B01J21/066B01J21/08B01J23/002
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Quick Facts
Patent No.
US 12,305,143
App. No.
17/608,733
Granted
May 20, 2025
Kind
B2
Abstract

Methods of using silica-zirconia catalysts in processes to reduce an amount of glycidol, glycidyl ester(s), or both glycidol and glycidyl ester(s) from a triglyceride-containing composition, such as edible oils, are disclosed. Silica-zirconia catalysts and methods of making silica-zirconia catalysts are also disclosed.

Claims (23)

1. A method for reducing an amount of (i) glycidol, (ii) glycidyl ester, or (iii) both glycidol and glycidyl ester within a composition comprising a triglyceride, said method comprising:

contacting the composition comprising a triglyceride with an effective amount of a particulate silica-zirconia catalyst to reduce the amount of (i) glycidol, (ii) glycidyl ester, or (iii) both glycidol and glycidyl ester in the composition, the silica-zirconia catalyst comprising porous silica particles impregnated with zirconia, wherein the porous silica particles comprise silica gel, precipitated silica, or fumed silica particles,

wherein the amount of (i) glycidol, (ii) glycidyl ester, or (iii) both glycidol and glycidyl ester is reduced without affecting other components of the composition comprising the triglyceride, and

wherein the containing step occurs at a temperature and a reaction time sufficient to reduce the amount of glycidol, glycidyl ester, or both glycidol and glycidyl ester in the composition by more than 95%.

2. The method of claim 1 , wherein the silica-zirconia catalyst comprises zirconia located on at least a portion of the surface of the porous silica particles.

3. The method of claim 1 , wherein the silica-zirconia catalyst comprises zirconia located in at least a portion of the pores of the porous silica particles or wherein the silica-zirconia catalyst comprises zirconia located substantially in the pores of the porous silica particles.

4. The method of claim 1 , wherein the silica-zirconia catalyst comprises particles having a median particle size of from about 0.1 micron (μm) to about 10,000 μm.

5. The method of claim 1 , wherein the silica-zirconia catalyst comprises particles having a pore volume of at least 0.01 cubic centimeters/gram (cc/g) as determined by Barrett-JoynerHalenda (BJH) method.

6. The method of claim 1 , wherein the silica-zirconia catalyst comprises particles having a median pore diameter of at least 0.1 nanometers (nm) up to about 1,000 nm as determined by a mercury intrusion test procedure using an Autopore IV 9520 available from Micromeritics Instrument Corp.

7. The method of claim 1 , wherein the silica-zirconia catalyst comprises particles having a BET particle surface area of at least about 10 m 2 /g up to about 2000 m 2 /g, or greater.

8. The method of claim 1 , wherein the silica-zirconia catalyst comprises particles comprising from about 1.0 wt % to about 50.0 wt % of zirconia based on a total weight of the silica-zirconia catalyst.

9. The method of claim 1 , wherein the silica-zirconia catalyst comprises particles formed by: impregnating porous silica particles with a soluble zirconium compound in water; drying the impregnated porous silica particles at about 105° C. for about 2 hours; and calcining the dried impregnated porous silica particles at about 500° C. for about 4 hours.

10. The method of claim 1 , further comprising: mixing the composition comprising the triglyceride and the silica-zirconia catalyst.

11. The method of claim 1 , further comprising: heating the composition comprising the triglyceride and the silica-zirconia catalyst up to a temperature of at least 40.0° C.

12. The method of claim 11 , wherein said heating step comprises: heating the composition comprising the triglyceride and the silica-zirconia catalyst up to an uppermost temperature; and maintaining the uppermost temperature for at least 10.0 minutes.

13. The method of claim 1 , wherein said contacting step comprises: mixing the composition comprising the triglyceride and the silica-zirconia catalyst under vacuum.

14. The method of claim 1 , wherein the composition comprising the triglyceride comprises (i) an edible oil, (ii) an organic solvent, or (iii) both an oil and an organic solvent.

15. The method of claim 1 , wherein the composition comprising the triglyceride comprises (i) a triglyceride-based oil, (ii) an organic solvent capable of dissolving triglycerides, or (iii) both a triglyceride-based oil and an organic solvent capable of dissolving triglycerides.

16. The method of claim 1 , wherein the composition comprising the triglyceride comprises soybean oil, palm oil, com oil, canola oil, rapeseed oil, fish oil, algal oil, sunflower oil, olive oil, vegetable oil, plant-derived oil, animal-derived oil, microbial-derived oil, or any combination thereof.

17. The method of claim 1 , wherein the composition comprising the triglyceride further comprises heptane, hexane, toluene, diethyl ether, an alcohol, or any combination thereof.

18. The method of claim 1 , wherein the glycidyl ester within the composition comprising the triglyceride comprises glycidyl oleate.

19. The method of claim 1 , wherein the amount of silica-zirconia catalyst comprises from about 0.5 wt % to about 10.0 wt % of the silica-zirconia catalyst based on a total weight of the silica zirconia catalyst and the composition comprising the triglyceride.

20. The method of claim 1 , wherein the method reduces the amount of (i) glycidol, (ii) glycidyl ester, or (iii) both glycidol and glycidyl ester to a level of less than 10.0 parts per million (ppm) of (i) glycidol, (ii) glycidyl ester, or (iii) both glycidol and glycidyl ester in the composition comprising the triglyceride.

Assignments (8)
RELEASE OF SECURITY INTEREST SUPPLEMENT NO. 1, RECORDED AT REEL/FRAME 063237/0252 Recorded Feb 2, 2026
From: WILMINGTON TRUST, NATIONAL ASSOCIATION
To: W. R. GRACE & CO.-CONN.
Reel/Frame 074612/0939 →
NOTES SECURITY INTEREST Recorded Jan 29, 2026
From: W. R. GRACE & CO.-CONN.; ADVANCED REFINING TECHNOLOGIES LLC
To: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS NOTES COLLATERAL AGENT
Reel/Frame 074532/0229 →
SECURITY AGREEMENT (NOTES) Recorded Aug 19, 2025
From: W. R. GRACE & CO.-CONN.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS NOTES COLLATERAL AGENT
Reel/Frame 072520/0653 →
SECURITY INTEREST Recorded Apr 2, 2023
From: W. R. GRACE & CO.-CONN.
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 063237/0262 →
SECURITY INTEREST Recorded Apr 2, 2023
From: W. R. GRACE & CO.-CONN.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 063237/0252 →
SECURITY INTEREST Recorded Feb 17, 2023
From: W.R. GRACE & CO.-CONN.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 062792/0510 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 1, 2022
From: MICHOS, DEMETRIUS; GRIMES, CHELSEA L; LIBANATI, CRISTIAN; CATUCCI, IGNAZIO
To: W.R. GRACE & CO.-CONN.
Reel/Frame 060418/0283 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 6, 2022
From: GRIMES, CHELSEA; MICHOS, DEMETRIUS; LIBANATI, CRISTIAN; CATUCCI, IGNAZIO
To: W.R. GRACE & CO.-CONN.
Reel/Frame 059517/0901 →