IP Library Granted Patent US 8,334,006
Granted Patent B2
US 8,334,006 · App. 12/720,888 · Granted Dec 18, 2012

Process for manufacturing a sweetener and use thereof

Assignee: Purecircle SDN BHD
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Quick Facts
Patent No.
US 8,334,006
App. No.
12/720,888
Granted
Dec 18, 2012
Kind
B2
Abstract

Highly purified Stevioside, Rebaudioside A and a purified sweet steviol glycoside mixture were prepared from sweet glycoside extracts obtained from Stevia rebaudiana Bertoni leaves. The resulting sweeteners are suitable as non-calorie, non-cariogenic, non-bitter, non-lingering sweeteners, which may be advantageously applied in foods, beverages, and milk products.

Claims (47)

1. A process for producing a low-calorie sweetener composition, comprising the steps of:

a) drying Stevia rebaudiana leaves;

b) treating the dried Stevia rebaudiana leaves with water to extract sweet glycosides, wherein a leaves-water mixture is formed;

c) filtering the leaves-water mixture to obtain an aqueous filtrate;

d) directly treating the aqueous filtrate with calcium hydroxide or calcium oxide to raise the pH of the aqueous filtrate to about 10;

e) directly neutralizing the treated aqueous filtrate with trivalent iron chloride; and

f) filtrating the neutralized aqueous filtrate to obtain a filtrated aqueous filtrate, and evaporating the filtrated aqueous filtrate to dryness to obtain purified sweet glycosides to provide a high intensity sweetener;

g) providing sugar granules as a low intensity sweetener;

h) adjusting a moisture content of the sugar granules to a level of about 0.5% to about 1.5%;

i) distributing the sugar granules on a vibrating surface to form a layer with thickness of about 10 to about 100 mm on the vibrating surface;

j) dissolving the high intensity sweetener in an aqueous alcohol mixture with an alcohol content of about 0.1% to about 99.9% (v/v) to obtain a solution with about 10% to about 70% (w/w) solids to make a high intensity sweetener solution;

k) dispersing the high intensity sweetener solution onto the sugar granules while maintaining an intensity of vibration at about 1 to about 2000 vpm; and

l) drying the granules to form the low-calorie sweetener composition.

2. The process of claim 1 , wherein a dry weight ratio of the low intensity sweetener to high intensity sweetener is in the range of about 50:1 to about 300:1 (w/w).

3. A process for making a low-calorie sweetener, comprising the steps of:

a) drying Stevia rebaudiana leaves;

b) treating the dried Stevia rebaudiana leaves with water to extract sweet glycosides, wherein a leaves-water mixture is formed;

c) filtering the leaves-water mixture to obtain an aqueous filtrate;

d) directly treating the aqueous filtrate with calcium hydroxide or calcium oxide to raise the pH of the aqueous filtrate to about 10;

e) directly neutralizing the treated aqueous filtrate with trivalent iron chloride; and

f) filtrating the neutralized aqueous filtrate to obtain a filtrated aqueous filtrate, and evaporating the filtrated aqueous filtrate to dryness to obtain purified sweet glycosides as a high intensity sweetener;

g) providing sugar granules as a low intensity sweetener;

h) making a sweetener blend by combining the low intensity sweetener with the high intensity sweetener in a ribbon blender;

i) compacting the sweetener blend into a sweetener sheet using a roll compaction unit; and

j) milling the sweetener sheet into granules to make the low-calorie sweetener.

4. A process for making a low-calorie sweetener, comprising the steps of:

a) drying Stevia rebaudiana leaves;

b) treating the dried Stevia rebaudiana leaves with water to extract sweet glycosides, wherein a leaves-water mixture is formed;

c) filtering the leaves-water mixture to obtain an aqueous filtrate;

d) directly treating the aqueous filtrate with calcium hydroxide or calcium oxide to raise the pH of the aqueous filtrate to about 10;

e) directly neutralizing the treated aqueous filtrate with trivalent iron chloride; and

f) filtrating the neutralized aqueous filtrate to obtain a filtrated aqueous filtrate, and evaporating the filtrated aqueous filtrate to dryness to obtain purified sweet glycosides as a high intensity sweetener;

g) providing sugar granules as a low intensity sweetener;

h) making a sweetener solution by combining the low intensity sweetener, the high intensity sweetener and water;

i) passing the sweetener solution through multiple-effect evaporators to make an evaporated sweetener solution;

j) applying a vacuum to the evaporated sweetener solution to make a super-saturated solution;

k) seeding the super-saturated solution with an additional amount of the low intensity sweetener to initiate crystal formation;

l) allowing crystal formation to continue to complete crystallization in the solution; and

m) separating the crystals from the solution to result in the low-calorie sweetener.

5. The process of claim 3 , wherein a dry weight ratio of the low intensity sweetener to high intensity sweetener is in the range of about 50:1 to about 300:1 (w/w).

6. The process of claim 4 , wherein a dry weight ratio of the low intensity sweetener to high intensity sweetener is in the range of about 50:1 to about 300:1 (w/w).

7. The process of claim 1 , wherein the purified sweet glycosides obtained in step (f) are dissolved in methanol at temperatures ranging from about 20-50° C., in an amount of 1:2-1:7 (w/v) to precipitate Stevioside from solution, filtering the solution to recover Stevioside precipitate, suspending the precipitate in an alcohol-water solution to further purify the Stevioside, and recovering the higher purity of Stevioside with a purity of at least 98% to provide the high intensity sweetener.

8. The process of claim 7 , further comprising the steps of combining remaining alcohol solutions, removing the alcohol, ultrafiltering to obtain a filtrate, recovering Rebaudioside A, mixing the Rebaudioside A with dilute alcohol, and filtering and drying to result in Rebaudioside A with a purity of at least 98% to provide the high intensity sweetener.

9. The process of claim 3 , wherein the purified sweet glycosides obtained in step (f) are dissolved in methanol at temperatures ranging from about 20-50° C., in an amount of 1:2-1:7 (w/v) to precipitate Stevioside from solution, filtering the solution to recover Stevioside precipitate, suspending the precipitate in an alcohol-water solution to further purify the Stevioside, and recovering the higher purity of Stevioside with a purity of at least 98% to provide the high intensity sweetener.

10. The process of claim 9 , further comprising the steps of combining remaining alcohol solutions, removing the alcohol, ultrafiltering to obtain a filtrate, recovering Rebaudioside A, mixing the Rebaudioside A with dilute alcohol, and filtering and drying to result in Rebaudioside A with a purity of at least 98% to provide the high intensity sweetener.

11. The process of claim 4 , wherein the purified sweet glycosides obtained in step (f) are dissolved in methanol at temperatures ranging from about 20-50° C., in an amount of 1:2-1:7 (w/v) to precipitate Stevioside from solution, filtering the solution to recover Stevioside precipitate, suspending the precipitate in an alcohol-water solution to further purify the Stevioside, and recovering the higher purity of Stevioside with a purity of at least 98% to provide the high intensity sweetener.

12. The process of claim 11 , further comprising the steps of combining remaining alcohol solutions, removing the alcohol, ultrafiltering to obtain a filtrate, recovering Rebaudioside A, mixing the Rebaudioside A with dilute alcohol, and filtering and drying to result in Rebaudioside A with a purity of at least 98% to provide the high intensity sweetener.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 15, 2010
From: PURKAYASTHA, SIDDHARTHA; MARKOSYAN, AVETIK; MALSAGOV, MAGOMET
To: PURECIRCLE SDN BHD
Reel/Frame 024537/0899 →
Continuity (8)
Continuation In Part 11246066 · Oct 11, 2005
Continuation In Part 11246152 · Oct 11, 2005
Continuation In Part 12684129 · Jan 8, 2010
Continuation In Part 12684130 · Jan 8, 2010
Continuation In Part 12684981 · Jan 11, 2010
Provisional Application 61260593 · Nov 12, 2009
Provisional Application 61290778 · Dec 29, 2009
Related Publication 20100227034A1 · Sep 9, 2010