IP Library › Granted Patent US 6,993,934
Granted Patent B2
US 6,993,934 · App. 10/657,455 · Granted Feb 7, 2006

Dental glass powders

Assignee: Cabot Corporation
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 6,993,934
App. No.
10/657,455
Granted
Feb 7, 2006
Kind
B2
Abstract

Dental glass powders, methods for producing the powders and dental compositions including the glass powders. The powders preferably have a well-controlled particle size, narrow size distribution and a spherical morphology. The method includes forming the particles by a spray pyrolysis technique. The invention also includes dental filler and restorative compositions that include the glass powders.

Claims (31)

1. A method for the production of dental glass particles, comprising the steps of:

a) generating an aerosol of droplets from a liquid wherein said liquid comprises a precursor to barium oxide, boron oxide, alumina and silica;

b) moving said droplets in a carrier gas;

c) pyrolyzing said droplets at a reaction temperature of from about 1000° C. to 1500° C. and for a residence time sufficient to remove liquid therefrom and convert said precursor to spherical barium boroaluminosilicate glass particles having a refractive index from about 1.40 to about 1.60; and

d) treating said glass particles to increase the surface area of said particles by at least 100 percent.

2. A method as recited in claim 1 , wherein said step of generating an aerosol comprises the step of ultrasonically atomizing said liquid.

3. A method as recited in claim 1 , wherein said carrier gas comprises air.

4. A method as recited in claim 1 , wherein said reaction temperature is from about 1000° C. to about 1300° C.

5. A method as recited in claim 1 , wherein said reaction temperature is from about 1150° C. to about 1250° C.

6. A method as recited in claim 1 , wherein said glass particles comprise not greater than about 0.1 atomic percent impurities.

7. A method as recited in claim 1 , wherein said glass particles have a particle density of at least about 95 percent of the theoretical density.

8. A method as recited in claim 1 , wherein said droplets in said aerosol have a size distribution such that no greater than about 30 weight percent of the droplets in said aerosol are larger than about twice the weight average droplet size.

9. A method as recited in claim 1 , wherein said barium oxide precursor comprises barium nitrate.

10. A method as recited in claim 1 , wherein said alumina precursor comprises aluminum nitrate.

11. A method as recited in claim 1 , wherein said boron oxide precursor comprises boric acid.

12. A method as recited in claim 1 , wherein said silica precursor comprises particulate silica.

13. A method as recited in claim 1 , wherein said method further comprises the step of annealing said glass particles.

14. A method as recited in claim 1 , wherein said method further comprises the step of coating said glass particles.

15. A method as recited in claim 1 , wherein said treating step comprises the step of contacting said glass particles with a basic solution or an acidic solution for a time sufficient to increase the surface area by at least about 100 percent.

16. A method as recited in claim 1 , further comprising the step of silanating said glass particles.

17. A method as recited in claim 1 , further comprising the steps of:

(e) contacting said glass particles with an aqueous environment to form hydroxyl groups on the surface of said glass particles; and

(f) silanating the surface of said glass particles.

18. A method for the production of dental glass particles, comprising the steps of:

(a) providing a batch of spherical glass particles having an average size of not greater than about 5 μm;

(b) treating the surface of said glass particles to increase the surface area of the glass particles by at least about 100 percent without substantially altering the bulk morphology of said particles;

(c) hydrolyzing the surface of said glass particles; and

(d) silanating the surface of said glass particles.

19. A method as recited in claim 18 , wherein said glass is an aluminosilicate glass.

20. A method as recited in claim 18 , wherein said treating step comprises contacting said glass particles with a basic solution or an acidic solution.

21. A method as recited in claim 18 , wherein said hydrolyzing step comprises contacting said glass particles with an aqueous environment for a time sufficient to form at least about 7 hydroxyl groups per square nanometer of glass surface area.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 1, 2005
From: NANOCHEM RESEARCH LLC
To: SUPERIOR MICROPOWDERS LLC
Reel/Frame 016333/0353 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 1, 2005
From: SUPERIOR MICROPOWDERS LLC
To: CABOT CORPORATION
Reel/Frame 016333/0409 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 29, 2005
From: KODAS, TOIVO T; HAMPDEN-SMITH, MARK J.; BREWSTER, JAMES H; POWELL, QUINT H; SKAMSER, DANIEL J; KUNZE, KLAUS; ATANASSOVA, PAOLINA; NAPOLITANO, PAUL
To: SUPERIOR MICROPOWDERS LLC
Reel/Frame 016328/0235 →
Continuity (3)
Division 0952048800 · Mar 8, 2000
Continuation In Part 0914139400 · Aug 27, 1998
Related Publication 20040134230A1 · Jul 15, 2004