IP Library Granted Patent US 7,306,788
Granted Patent B2
US 7,306,788 · App. 10/996,541 · Granted Dec 11, 2007

High-cleaning/moderate abrasive silica materials and dentifrice containing such materials

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Quick Facts
Patent No.
US 7,306,788
App. No.
10/996,541
Granted
Dec 11, 2007
Kind
B2
Abstract

Unique abrasive and/or thickening materials that are in situ generated compositions of precipitated silicas and silica gels are provided. Such compositions exhibit different beneficial characteristics depending on the structure of the composite in situ generated material. With low structured composites (as measured via linseed oil absorption levels from 40 to 100 ml oil absorbed/100 g composite), simultaneously high pellicle film cleaning properties and moderate dentin abrasion levels are possible in order to accord the user a dentifrice that effectively cleans tooth surfaces without detrimentally abrading such surfaces. Increased amounts of high structure composite materials tend to accord greater viscosity build and thickening benefits together with such desirable abrasion and cleaning properties, albeit to a lesser extent than for the low structure types. Thus, mid-range cleaning materials will exhibit oil absorption levels from an excess of 100 to 150, and high thickening/low abrasion composite exhibit oil absorption properties in excess of 150. Such an in situ, simultaneously produced precipitated silica/silica gel combination provides such unexpectedly effective low abrasion and high cleaning capability and different thickening characteristics as compared to physical mixtures of such components. Encompassed within this invention is a unique method for making such gel/precipitated silica composite materials for such a purpose, as well as the different materials within the structure ranges described above and dentifrices comprising such.

Claims (24)

1. An in situ produced gel/precipitate silica composite, wherein said composite comprises from 5 to 50% by volume of silica gel, wherein said composite exhibits a linseed oil absorption of between 40 and 100 ml/100 g, and wherein said composite exhibits a 10% Brass Einlehner hardness value in the range between about 5 and 30 mg loss/100,000 revolutions.

2. The composite of claim 1 wherein said composite comprises from 10 to 30% by volume of silica gel.

3. The in situ produced gel/precipitate silica composite of claim 1 wherein said composite is in the form of particles exhibiting a median particle size range of from 3 to 20 microns.

4. The in situ produced gel/precipitate silica composite of claim 2 wherein said composite is in the form of particles exhibiting a median particle size range of from 3 to 20 microns.

5. A dentifrice formulation comprising the composite as defined in claim 1 .

6. A dentifrice formulation comprising the composite as defined in claim 2 .

7. A dentifrice formulation comprising the composite as defined in claim 3 .

8. The dentifrice formulation of claim 5 further comprising an abrasive material other than said composite.

9. The dentifrice formulation of claim 6 further comprising an abrasive material other than said composite.

10. The dentifrice formulation of claim 7 further comprising an abrasive material other than said composite.

11. A method of producing the composite as defined in claim 1 , said method comprising the sequential steps of

a) admixing a sufficient amount of an alkali silicate having a concentration of from 4 to 35% by weight within an aqueous solution thereof and an acidulating agent having an acid concentration within an aqueous solution from 5 to 25% by weight together at a temperature from about 40 to about 90° C. and under agitation to form a composition comprising silica gel particles; and, without first washing, modifying, or purifying said formed composition comprising silica gel particles,

b) subsequently introducing to said composition comprising silica gel particles a sufficient amount of an alkali silicate and an acidulating agent to form a precipitated silica, thereby producing a gel/precipitate silica composite, wherein the pH of the overall reaction is within the range of from 3 to 10.

12. The method of claim 11 wherein the acid concentration in step “a” is from 10 to 20% by weight.

13. An in situ produced gel/precipitate silica composite, wherein said composite comprises from 5 to 50% by volume of silica gel, wherein when said composite is introduced as the sole abrasive component within a test dentifrice composition said dentifrice composition exhibits a PCR:RDA (Pellicle Cleaning Ratio: Radioactive Dentin Abrasion) ratio of from about 0.45 to about 0.7, a PCR value between about 90 and 160, and a RDA level of at most 240.

14. The composite of claim 13 wherein said composite comprises from 10 to 30% by volume of silica gel.

15. A dentifrice formulation comprising the composite as defined in claim 13 .

16. A dentifrice formulation comprising the composite as defined in claim 14 .

17. The dentifrice formulation of claim 15 further comprising an abrasive material other than said composite.

18. The dentifrice formulation of claim 16 further comprising an abrasive material other than said composite.

19. A method of producing the composite as defined in claim 13 , said method comprising the sequential steps of

a) admixing a sufficient amount of an alkali silicate having a concentration of from 4 to 35% by weight within an aqueous solution thereof and an acidulating agent having an acid concentration within an aqueous solution from 5 to 25% by weight together at a temperature from about 40 to about 90° C. and under agitation to form a composition comprising silica gel particles; and, without first washing, modifying, or purifying said formed composition comprising silica gel particles,

b) subsequently introducing to said composition comprising silica gel particles a sufficient amount of an alkali silicate and an acidulating agent to form a precipitated silica, thereby producing a gel/precipitate silica composite, wherein the pH of the overall reaction is within the range of from 3 to 10.

20. The method of claim 19 wherein the acid concentration in step “a” is from 10 to 20% by weight.

Assignments (3)
SECURITY INTEREST Recorded Nov 8, 2011
From: J.M. HUBER CORPORATION; CP KELCO U.S., INC.; HUBER ENGINEERED WOODS LLC
To: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS AGENT
Reel/Frame 027279/0114 →
RELEASE OF SECURITY INTEREST Recorded Nov 1, 2011
From: BANK OF AMERICA, N.A.
To: J.M. HUBER CORPORATION; 333 ASSOCIATES LLC; 333 PARTNERS LLC; CELTEGAN LLC; CP KELCO U.S., INC.; HUBER CST COMPANY; HUBER CST CORPORATION; HUBER ENERGY L.P.; HUBER ENERGY LLC; HUBER ENGINEERED WOODS LLC; HUBER EQUITY CORPORATION; HUBER INTERNATIONAL CORP.; HUBER RESOURCES CORP.; HUBER SOUTH TEXAS GP, LLC; HUBER SOUTH TEXAS LP, LLC; HUBER TIMBER INVESTMENTS LLC; HUBER TIMBER LLC; J.M. HUBER MICROPOWDERS INC.; JMH PARTNERS CORP.; KELCO COMPANY; ST. PAMPHILE TIMBER LLC; TABSUM, INC.; TARA INSURANCE GLOBAL LIMITED; QUINCY WAREHOUSES, INC. (FORMERLY UNDERGROUND WAREHOUSES, INC.
Reel/Frame 027158/0142 →
SECURITY AGREEMENT Recorded Mar 29, 2011
From: J.M. HUBER CORPORATION; 333 ASSOCIATES LLC; 333 PARTNERS LLC; CELTEGAN LLC; CP KELCO U.S., INC.; HUBER CST COMPANY; HUBER CST CORPORATION; HUBER ENERGY L.P.; HUBER ENERGY LLC; HUBER ENGINEERED WOODS LLC; HUBER EQUITY CORPORATION; HUBER INTERNATIONAL CORP.; HUBER RESOURCES CORP.; HUBER SOUTH TEXAS GP, LLC; HUBER SOUTH TEXAS LP, LLC; HUBER TIMBER INVESTMENTS LLC; HUBER TIMBER LLC; J.M. HUBER MICROPOWDERS INC.; JMH PARTNERS CORP.; KELCO COMPANY; ST. PAMPHILE TIMBER LLC; TABSUM, INC.; TARA INSURANCE GLOBAL LIMITED; UNDERGROUND WAREHOUSES, INC.
To: BANK OF AMERICA, N.A.
Reel/Frame 026042/0063 →