IP Library Granted Patent US 8,197,878
Granted Patent B2
US 8,197,878 · App. 13/106,429 · Granted Jun 12, 2012

Method for producing a low sodium salt composition

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Quick Facts
Patent No.
US 8,197,878
App. No.
13/106,429
Granted
Jun 12, 2012
Kind
B2
Abstract

The present invention relates to a low sodium salt composition and the methods used to make it. The low sodium salt composition includes sodium chloride and a modified chloride salt composition. The modified chloride salt composition includes a homogenous amalgamation of chloride salt, food grade acidulant, and carrier, which does not contain sodium chloride. The low sodium salt composition is made using a two step process. The first step includes making a modified chloride salt composition and the second step includes combining the modified chloride salt composition with sodium chloride to form a low sodium salt composition.

Claims (68)

1. A method of making a modified chloride salt composition, comprising:

a. contacting chloride salt with a food grade acidulant in an aqueous solution to form a liquid chloride salt product, wherein the chloride salt is not sodium chloride; and,

b. adding a carrier to the liquid chloride salt product to form a liquid modified chloride salt product, wherein the liquid modified chloride salt product is a homogenous amalgamation of chloride salt, food grade acidulant, and carrier.

2. The method of claim 1 , further comprising drying the liquid modified chloride salt product to form a granular modified chloride salt product.

3. The method of claim 1 , further comprising blending the modified chloride salt composition with sodium chloride to form a low sodium salt composition.

4. The method of claim 1 , wherein the composition comprises from about 15% to about 30% by weight chloride salt.

5. The method of claim 1 , wherein the composition comprises from about 0.1% to about 3% by weight food grade acidulant.

6. The method of claim 1 , wherein the composition comprises from about 10% to about 25% by weight carrier.

7. The method of claim 1 , wherein the chloride salt is selected from the group consisting of a chloride of potassium, magnesium, calcium, ammonium, and combinations thereof.

8. The method of claim 7 , wherein the chloride salt is magnesium and potassium chloride.

9. The method of claim 7 , wherein the chloride salt is potassium chloride.

10. The method of claim 1 , wherein the food grade acidulant is selected from the group consisting of citric acid, malic acid, tartaric acid, fumaric acid, lactic acid, acetic acid, benzoic acid, and combinations thereof.

11. The method of claim 10 , wherein the food grade acidulant is citric acid.

12. The method of claim 1 , wherein the carrier is selected from the group consisting of a starch molecule and a cereal starch.

13. The method of claim 12 , wherein the carrier is a starch molecule.

14. The method of claim 13 , wherein the starch molecule is selected from the group consisting of a dextrin, maltodextrin, monosaccharide, and combinations thereof.

15. The method of claim 14 , wherein the carrier is a maltodextrin.

16. The method of claim 14 , wherein the carrier is a monosaccharide.

17. The method of claim 16 , wherein the monosaccharide is selected from the group consisting of sucrose, glucose, xylose, ribose and combinations thereof.

18. The method of claim 12 , wherein the carrier is a cereal starch.

19. The method of claim 18 , wherein the cereal starch is selected from the group consisting of rice starch, rice cereal, rice flour and combinations thereof.

20. The method of claim 1 , further comprising an additive selected from the group consisting of antioxidant, phosphate, colorant, anti-caking agent and combinations thereof.

21. The method of claim 2 , wherein the drying step includes a technique selected from the group consisting of spray drying and drum drying.

22. A method of making a low sodium salt composition, comprising:

a. contacting chloride salt with a food grade acidulant and a carrier in an aqueous solution to form a liquid modified chloride salt product, wherein the chloride salt is not sodium chloride, wherein the carrier is added after the chloride salt and food grade acidulant are mixed, and wherein the liquid modified chloride salt product is a homogenous amalgamation of chloride salt, food grade acidulant, and carrier; and,

b. blending the liquid modified chloride salt product with sodium chloride to form a low salt composition.

23. The method of claim 22 , further comprising drying the liquid modified chloride salt product to form a granular carrier modified chloride salt product, wherein the liquid modified chloride salt product is dried before the blending with sodium chloride.

24. The method of claim 22 , wherein the composition comprises from about 15% to about 30% by weight chloride salt.

25. The method of claim 22 , wherein the composition comprises from about 0.1% to about 3% by weight food grade acidulant.

26. The method of claim 22 , wherein the composition comprises from about 10% to about 25% by weight carrier.

27. The method of claim 22 , wherein the aqueous solution includes the addition of from about 60% to about 80% water.

28. The method of claim 22 , wherein the chloride salt is selected from the group consisting of a chloride of potassium, magnesium, calcium, ammonium, and combinations thereof.

29. The method of claim 28 , wherein the chloride salt is magnesium and potassium chloride.

30. The method of claim 28 , wherein the chloride salt is potassium chloride.

31. The method of claim 22 , wherein the food grade acidulant is selected from the group consisting of citric acid, malic acid, tartaric acid, fumaric acid, lactic acid, acetic acid, and benzoic acid.

32. The method of claim 31 , wherein the food grade acidulant is citric acid.

33. The method of claim 22 , wherein the carrier is selected from the group consisting of a starch molecule and a cereal starch.

34. The method of claim 33 , wherein the carrier is a starch molecule.

35. The method of claim 34 , wherein the starch molecule is selected from the group consisting of a dextrin, maltodextrin, monosaccharide, and combinations thereof.

36. The method of claim 35 , wherein the carrier is a maltodextrin.

37. The method of claim 35 , wherein the carrier is a monosaccharide.

38. The method of claim 37 , wherein the monosaccharide is selected from the group consisting of sucrose, glucose, xylose, ribose and combinations thereof.

39. The method of claim 33 , wherein the carrier is a cereal starch.

40. The method of claim 39 , wherein the cereal starch is selected from the group consisting of rice starch, rice cereal, rice flour and combinations thereof.

41. The method of claim 22 , further comprising an additive selected from the group consisting of an antioxidant, phosphate, colorant, anti-caking agent, and combinations thereof.

42. The method of claim 23 , wherein the drying step includes a technique selected from the group consisting of spray drying and drum drying.

43. A method of making a low sodium salt composition, comprising:

a. contacting chloride salt with a food grade acidulant and a carrier in an aqueous solution to form a liquid modified chloride salt product, wherein the chloride salt is not sodium chloride, wherein the carrier is added after the chloride salt and food grade acidulant are mixed, and wherein the liquid modified chloride salt product is a homogenous amalgamation of chloride salt, modifier, and carrier;

b. drying the liquid modified chloride salt product to form a granular carrier modified chloride salt product; and,

c. blending the liquid modified chloride salt product with sodium chloride to form a low sodium salt composition.

44. The method of claim 43 , wherein the composition comprises from about 15% to about 30% by weight chloride salt.

45. The method of claim 43 , wherein the composition comprises from about 0.1% to about 3% by weight food grade acidulant.

46. The method of claim 43 , wherein the composition comprises from about 10% to about 25% by weight carrier.

47. The method of claim 43 , wherein the aqueous solution includes the addition of from about 60% to about 80% water.

48. The method of claim 43 , wherein the chloride salt is selected from the group consisting of a chloride of potassium, magnesium, calcium, ammonium, and a mixture thereof.

49. The method of claim 48 , wherein the chloride salt is magnesium and potassium chloride.

50. The method of claim 48 , wherein the chloride salt is potassium chloride.

51. The method of claim 43 , wherein the food grade acidulant is selected from the group consisting of citric acid, malic acid, tartaric acid, fumaric acid, lactic acid, acetic acid, and benzoic acid.

52. The method of claim 51 , wherein the food grade acidulant is citric acid.

53. The method of claim 43 , wherein the carrier is selected from the group consisting of a starch molecule and a cereal starch.

54. The method of claim 53 , wherein the carrier is a starch molecule.

55. The method of claim 54 , wherein the starch molecule is selected from the group consisting of a dextrin, maltodextrin, monosaccharide, and combinations thereof.

56. The method of claim 55 , wherein the carrier is a maltodextrin.

57. The method of claim 55 , wherein the carrier is a monosaccharide.

58. The method of claim 57 , wherein the monosaccharide is selected from the group consisting of sucrose, glucose, xylose, ribose and combinations thereof.

59. The method of claim 53 , wherein the carrier is a cereal starch.

60. The method of claim 59 , wherein the cereal starch is selected from the group consisting of rice starch, rice cereal, rice flour and combinations thereof.

61. The method of claim 43 , further comprising an additive selected from the group consisting of an antioxidant, phosphate, colorant, anti-caking agent, and combinations thereof.

Assignments (8)
RELEASE OF SECURITY INTEREST Recorded Jun 2, 2022
From: PROTERRA FINANCE LLC, AS COLLATERAL AGENT
To: S & P INGREDIENT DEVELOPMENT, LLC
Reel/Frame 060088/0345 →
SECURITY AGREEMENT Recorded May 27, 2022
From: S & P INGREDIENT DEVELOPMENT, LLC
To: BMO HARRIS BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 060204/0584 →
RELEASE OF SECURITY INTEREST Recorded May 4, 2021
From: COMERICA BANK
To: S & P INGREDIENT DEVELOPMENT, LLC
Reel/Frame 056129/0794 →
SECURITY INTEREST Recorded Apr 30, 2021
From: S & P INGREDIENT DEVELOPMENT, LLC
To: PROTERRA FINANCE LLC, AS COLLATERAL AGENT
Reel/Frame 056096/0081 →
SECURITY INTEREST Recorded Mar 17, 2016
From: S & P INGREDIENT DEVELOPMENT, LLC
To: COMERICA BANK
Reel/Frame 038135/0942 →
CORRECTIVE ASSIGNMENT TO CORRECT THE OMISSION OF INVENTOR/ASSIGNOR MICHAEL G. FAHEY ASSIGNMENT EXECUTED ON AUGUST 2, 2011 PREVIOUSLY RECORDED ON REEL 026816 FRAME 0345. ASSIGNOR(S) HEREBY CONFRIMS THE ASSIGNMENT OF ALL OF ASSIGNOR'S RIGHT, TITLE AND INTEREST. Recorded Oct 28, 2011
From: CHIGURUPATI, SAMBASIVA RAO; MANUEL, THOMAS L.; FAHEY, MICHAEL G.
To: S & P INGREDIENT DEVELOPMENT, LLC
Reel/Frame 027145/0358 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 26, 2011
From: CHIGURUPATI, SAMBASIVA RAO
To: CHIGURUPATI, SAMBASIVA RAO; MANUEL, THOMAS L.; FAHEY, MICHAEL G.
Reel/Frame 026816/0287 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 26, 2011
From: CHIGURUPATI, SAMBASIVA RAO; MANUEL, THOMAS L.
To: S & P INGREDIENT DEVELOPMENT, LLC
Reel/Frame 026816/0345 →