IP Library Granted Patent US 12,331,261
Granted Patent B2
US 12,331,261 · App. 16/681,232 · Granted Jun 17, 2025

Composition and method of manufacturing sulfonate-based greases using a glycerol derivative

Inventors: J. Andrew Waynick (Lantana, TX); Gaston Aguilar (Farmers Branch, TX)
Assignee: NCH Corporation
C10M169/02C10M105/38C10M125/10C10M125/24C10M125/26C10M129/32C10M129/44C10M135/10C10M141/02C10M2201/062C10M2201/08C10M2201/085C10M2201/087C10M2207/122C10M2207/128C10M2207/2835C10M2219/0466C10N2050/10
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Quick Facts
Patent No.
US 12,331,261
App. No.
16/681,232
Granted
Jun 17, 2025
Kind
B2
Abstract

A sulfonate-based grease composition and method of manufacture comprising the addition of one or more glycerol derivatives. The glycerol derivative acts to optimally disperse the thickener in the grease such that the conventional step of milling the grease may not be needed. The glycerol derivative reacts with water to form in-situ complexing acids, which may replace at least some of the normally used complexing acids for reacting with calcium containing bases. The greases according to preferred embodiments have a high dropping point, improved thickener yield, and faster conversion time.

Claims (93)

1. A method for making a complex sulfonate-based grease comprising the steps of:

adding and mixing (1) 33% or less overbased calcium sulfonate having amorphous calcium carbonate dispersed therein and (2) water;

adding and mixing 0.1 to 5% of one or more conventional non-aqueous converting agents after a converting agent delay period comprising (1) a converting agent holding delay period wherein a mixture comprising the overbased calcium sulfonate and the water is maintained at a temperature or within a range of temperatures for a period of time of at least 20 minutes or (2) a converting agent temperature adjustment delay period where the mixture comprising the overbased calcium sulfonate and the water is heated or (3) a combination thereof;

converting a mixture comprising the overbased calcium sulfonate, the water, and the one or more conventional non-aqueous converting agents by heating until conversion of the amorphous calcium carbonate contained in the overbased calcium sulfonate to a crystalline form has occurred;

adding and mixing 1.25 to 18% total of one or more complexing acids prior to the converting step, during the converting step, or after the converting step;

adding and mixing 1 to 20% total of one or more calcium containing bases prior to the converting step, during the converting step, or after the converting step; and

adding and mixing 0.1 to 6% of a glycerol derivative after the converting step, wherein the addition of the glycerol derivative forms an acid reaction product from hydrolyzing the glycerol derivative, wherein no glycerol derivative is added prior to the converting step, and wherein the glycerol derivative comprises (1) glycerol mono-oleate, (2) hydrogenated castor oil, (3) glycerol mono-stearate, (4) glycerol mono-tallowate, or (5) a combination thereof;

adding and mixing an alkali metal hydroxide after the converting step, wherein no alkali metal hydroxide is added prior to the converting step;

heating to a temperature sufficient to remove the water;

wherein the percentages are by weight.

2. The method of claim 1 further comprising adding and mixing a facilitating acid prior to the converting step;

wherein the one or more complexing acids comprise 12-hydroxystearic acid, acetic acid, and phosphoric acid;

wherein the one or more calcium containing bases comprise calcium hydroxyapatite, added calcium carbonate, added calcium hydroxide, or a combination thereof; and

wherein the one or more conventional non-aqueous converting agents comprise an alcohol, ether, glycol, glycol ether, glycol polyether, or combinations thereof.

3. The method of claim 2 wherein the adding and mixing the glycerol derivative step is after the adding and mixing the alkali metal hydroxide step.

4. The method of claim 3 wherein none of the one or more complexing acids are added between completion of the converting step and the adding and mixing the glycerol derivative step.

5. The method of claim 4 wherein the one or more complexing acids further comprise boric acid.

6. The method of claim 5 wherein a first portion of the 12-hydroxystearic acid and a first portion of the acetic acid are added prior to or during the converting step; and

wherein a second portion of the 12-hydroxystearic, a second portion of the acetic acid, all of the phosphoric acid, and all of the boric acid are added after the adding and mixing the glycerol derivative step.

7. The method of claim 6 wherein the calcium hydroxyapatite, a first portion of the added calcium carbonate, and a first portion of the added calcium hydroxide are added prior to the converting step;

wherein a second portion of the added calcium carbonate and a second portion of the added calcium hydroxide are added after the converting step; and

wherein the glycerol derivative comprises hydrogenated castor oil.

8. The method of claim 7 wherein no overbased magnesium sulfonate is added.

9. A method for making a complex sulfonate-based grease comprising the steps of:

adding and mixing (1) 33% or less overbased calcium sulfonate having amorphous calcium carbonate dispersed therein and (2) water;

adding and mixing 0.1 to 5% of one or more conventional non-aqueous converting agents after a converting agent delay period, wherein the one or more conventional non-aqueous converting agents comprise an alcohol, ether, glycol, glycol ether, glycol polyether, or combinations thereof and wherein the converting agent delay period comprises (1) a converting agent holding delay period wherein a mixture comprising the overbased calcium sulfonate and the water is maintained at a temperature or within a range of temperatures for a period of time of at least 20 minutes or (2) a converting agent temperature adjustment delay period where the mixture comprising the overbased calcium sulfonate and the water is heated or (3) a combination thereof;

converting a mixture comprising the overbased calcium sulfonate, the water, and the one or more conventional non-aqueous converting agents by heating until conversion of the amorphous calcium carbonate contained in the overbased calcium sulfonate to a crystalline form has occurred;

adding and mixing 1.25 to 18% total of one or more complexing acids, wherein the one or more complexing acids comprise 12-hydroxystearic acid, acetic acid, phosphoric acid, and boric acid;

adding and mixing 1 to 20% total of one or more calcium containing bases prior to the converting step, during the converting step, or after the converting step, wherein the one or more calcium containing bases comprise calcium hydroxyapatite, added calcium carbonate, added calcium hydroxide, or a combination thereof;

adding and mixing an alkali metal hydroxide after the converting step, wherein no alkali metal hydroxide is added prior to the converting step;

adding and mixing 0.1 to 1.0% of a glycerol derivative after the adding and mixing the alkali metal hydroxide step, wherein the addition of the glycerol derivative forms an acid reaction product from hydrolyzing the glycerol derivative, wherein no glycerol derivative is added prior to the converting step, and wherein the glycerol derivative comprises hydrogenated castor oil;

adding and mixing a facilitating acid prior to the converting step; and

heating to a temperature sufficient to remove the water;

wherein a first portion of the 12-hydroxystearic acid and a first portion of the acetic acid are added prior to or during the converting step; and

wherein a second portion of the 12-hydroxystearic, a second portion of the acetic acid, all of the phosphoric acid, and all of the boric acid are added after the adding and mixing the glycerol derivative step;

wherein none of the one or more complexing acids are added between completion of the converting step and the adding and mixing the glycerol derivative step;

wherein the calcium hydroxyapatite, a first portion of the added calcium carbonate, and a first portion of the added calcium hydroxide are added prior to the converting step;

wherein a second portion of the added calcium carbonate and a second portion of the added calcium hydroxide are added after the converting step;

wherein no overbased magnesium sulfonate is added; and

wherein the percentages are by weight.

10. The method of claim 9 wherein the overbased calcium sulfonate is a good quality overbased calcium sulfonate.

11. The method of claim 9 wherein the overbased calcium sulfonate is a poor quality overbased calcium sulfonate.

12. The method of claim 9 wherein the one or more conventional non-aqueous converting agents comprises hexylene glycol or propylene glycol or both.

13. The method of claim 9 wherein the overbased calcium sulfonate is a good quality overbased calcium sulfonate and wherein the one or more conventional non-aqueous converting agents comprises hexylene glycol.

14. The method of claim 9 wherein the overbased calcium sulfonate is a poor quality overbased calcium sulfonate and wherein the one or more conventional non-aqueous converting agents comprises hexylene glycol.

15. The method of claim 1 wherein the complex sulfonate-based grease has a dropping point of 575 F or higher.

16. The method of claim 1 wherein the complex sulfonate-based grease has a dropping point of 600 F or higher.

17. The method of claim 1 wherein the complex sulfonate-based grease has a dropping point of 650 F or higher.

18. The method of claim 1 wherein the glycerol derivative comprises the glycerol mono-stearate.

19. The method of claim 18 wherein the overbased calcium sulfonate is a poor quality overbased calcium sulfonate.

20. The method of claim 1 wherein the glycerol derivative comprises the hydrogenated castor oil and wherein the one or more complexing acids comprises 12-hydroxystearic acid.

21. The method of claim 20 wherein the overbased calcium sulfonate is a poor quality overbased calcium sulfonate.

22. The method of claim 1 wherein the overbased calcium sulfonate is a poor quality overbased calcium sulfonate.

23. The method of claim 1 wherein there is no milling step.

24. The method of claim 1 wherein the complex sulfonate-based grease has a first storage modulus curve G′ that has a first cross over point with a first loss modulus curve G″ in an unmilled state and a second storage modulus curve G′ that has a second cross over point with a second loss modulus curve G″ in an milled state; and

wherein the first and second cross over points are substantially the same with respect to relative shear strain.

25. A method for making a complex sulfonate-based grease comprising the steps of:

adding and mixing (1) 33% or less overbased calcium sulfonate having amorphous calcium carbonate dispersed therein and a Total Bae Number of 400 or higher, and (2) water;

adding and mixing 0.1 to 5% of one or more conventional non-aqueous converting agents after a converting agent delay period comprising (1) a converting agent holding delay period wherein a mixture comprising the overbased calcium sulfonate and the water is maintained at a temperature or within a range of temperatures for a period of time of at least 20 minutes or (2) a converting agent temperature adjustment delay period where the mixture comprising the overbased calcium sulfonate and the water is heated or (3) a combination thereof;

converting a mixture comprising the overbased calcium sulfonate, the water, and the one or more conventional non-aqueous converting agents by heating until conversion of the amorphous calcium carbonate contained in the overbased calcium sulfonate to a crystalline form has occurred;

adding and mixing 1.25 to 18% total of one or more complexing acids comprising 12-hystoxystearic acid prior to the converting step, during the converting step, or after the converting step;

adding and mixing 1 to 20% total of one or more calcium containing bases prior to the converting step, during the converting step, or after the converting step;

heating to a temperature sufficient to remove the water; and

adding and mixing 0.1 to 1.0% of a glycerol derivative prior to the heating to a temperature sufficient to remove the water step, wherein the addition of the glycerol derivative forms an acid reaction product from hydrolyzing the glycerol derivative with the water, and wherein the glycerol derivative comprises hydrogenated castor oil; and

wherein the percentages are by weight.

26. The method of claim 25 further comprising:

adding and mixing a facilitating acid prior to the converting step;

wherein the one or more complexing acids further comprise acetic acid, phosphoric acid, and boric acid; and

wherein 25% or less overbased calcium sulfonate is added and mixed.

27. The method of claim 26 wherein a first portion of the 12-hydroxystearic acid and a first portion of the acetic acid are added prior to or during the converting step;

wherein a second portion of the 12-hydroxystearic, a second portion of the acetic acid, all of the phosphoric acid, and all of the boric acid are added after the adding and mixing the glycerol derivative step; and

wherein 20% or less overbased calcium sulfonate is added and mixed.

28. The method of claim 27 wherein the calcium hydroxyapatite, a first portion of the added calcium carbonate, and a first portion of the added calcium hydroxide are added prior to the converting step;

wherein a second portion of the added calcium carbonate and a second portion of the added calcium hydroxide are added after the converting step; and

wherein around 16-21% overbased calcium sulfonate is added and mixed.

29. The method of claim 28 wherein no facilitating acid delay is used.

30. The method of claim 29 wherein no overbased magnesium sulfonate is added.

31. The method of claim 30 further comprising adding and mixing an alkali metal hydroxide after the converting step, wherein no alkali metal hydroxide is added prior to the converting step; and

wherein no glycerol derivative is added prior to the converting step.

32. The method of claim 31 wherein the one or more conventional non-aqueous converting agents comprises hexylene glycol.

33. The method of claim 1 wherein 0.1 to 1% of the glycerol derivative is added and mixed.

34. The method of claim 33 wherein 15-22% overbased calcium sulfonate having amorphous calcium carbonate dispersed therein is added and mixed.

35. The method of claim 33 wherein the overbased calcium sulfonate has a Total Base Number of 400 or higher.

36. The method of claim 8 wherein 0.7 to 1.0% of the glycerol derivative is added and mixed.

37. The method of claim 36 wherein 15-22% overbased calcium sulfonate having amorphous calcium carbonate dispersed therein is added and mixed.

38. The method of claim 36 wherein the overbased calcium sulfonate is a poor quality overbased calcium sulfonate.

39. The method of claim 38 wherein the complex sulfonate-based grease has a first storage modulus curve G′ that has a first cross over point with a first loss modulus curve G″ in an unmilled state and a second storage modulus curve G′ that has a second cross over point with a second loss modulus curve G″ in an milled state; and

wherein the first and second cross over points are substantially the same with respect to relative shear strain.

40. The method of claim 39 wherein there is no milling step.

41. The method of claim 36 wherein the overbased calcium sulfonate is a good quality overbased calcium sulfonate.

42. The method of claim 41 wherein the complex sulfonate-based grease has a first storage modulus curve G′ that has a first cross over point with a first loss modulus curve G″ in an unmilled state and a second storage modulus curve G′ that has a second cross over point with a second loss modulus curve G″ in an milled state; and

wherein the first and second cross over points are substantially the same with respect to relative shear strain.

43. The method of claim 42 wherein there is no milling step.

Assignments (7)
SECURITY INTEREST Recorded Nov 14, 2025
From: CHEM-AQUA, INC.; DIVERSEY, INC.; DIVERSEY TASKI, INC.; INNOVATIVE WATER CARE, LLC; NCH CORPORATION; NCH LIFE SCIENCES LLC; SOLENIS TECHNOLOGIES, L.P.
To: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A., AS NOTES COLLATERAL AGENT
Reel/Frame 073570/0838 →
SECURITY INTEREST Recorded Nov 14, 2025
From: CHEM-AQUA, INC.; NCH CORPORATION; NCH LIFE SCIENCES LLC
To: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A., AS NOTES COLLATERAL AGENT
Reel/Frame 073570/0763 →
SECURITY INTEREST Recorded Nov 14, 2025
From: CHEM-AQUA, INC.; NCH CORPORATION; NCH LIFE SCIENCES LLC
To: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A., AS NOTES COLLATERAL AGENT
Reel/Frame 073570/0920 →
SECURITY INTEREST Recorded Nov 14, 2025
From: CHEM-AQUA, INC.; NCH CORPORATION; NCH LIFE SCIENCES LLC
To: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A., AS NOTES COLLATERAL AGENT
Reel/Frame 073570/0750 →
SECURITY INTEREST Recorded Nov 14, 2025
From: CHEM-AQUA, INC.; DIVERSEY, INC.; INNOVATIVE WATER CARE, LLC; NCH CORPORATION; NCH LIFE SCIENCES LLC; SOLENIS TECHNOLOGIES, L.P.
To: BANK OF AMERICA, N.A., AS COLLATERAL AGENT
Reel/Frame 073564/0584 →
SECURITY INTEREST Recorded Nov 14, 2025
From: CHEM-AQUA, INC.; DIVERSEY, INC.; INNOVATIVE WATER CARE, LLC; NCH CORPORATION; NCH LIFE SCIENCES LLC; SOLENIS TECHNOLOGIES, L.P.
To: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
Reel/Frame 073564/0656 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 24, 2020
From: WAYNICK, J. ANDREW; AGUILAR, GASTON
To: NCH CORPORATION
Reel/Frame 053871/0941 →
Continuity (2)
Provisional Application 62769704 · Nov 20, 2018
Related Publication 20200157459A1 · May 21, 2020
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