IP Library Granted Patent US 7,758,977
Granted Patent B2
US 7,758,977 · App. 11/777,667 · Granted Jul 20, 2010

Crystalline zirconia and method of synthesis

Assignee: University of Central Florida Research Foundation, Inc.
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 7,758,977
App. No.
11/777,667
Granted
Jul 20, 2010
Kind
B2
Abstract

Novel, monodispersed, spherical ZrO 2 particles in the size range of approximately 10 to approximately 600 nm exhibiting metastable tetragonal crystal structure at room temperature and novel methods of preparation. The ZrO 2 particles are approximately 100% in the tetragonal phase at room temperature and can be pure and free of foreign oxides. The novel method can include mixing zirconium-alkoxide and an alcohol, forming preparation one, followed by separately dissolving completely de-ionized water and a polymeric steric stabilizer in an alcohol forming preparation two. Next the preparations can be mixed with vigorous stirring while subjecting the materials to hydrolysis and condensation reactions with very slow stirring. Next, there is waiting for the formation of a sol from the mixture, followed by drying at approximately 80 degrees C. to form resultant material followed by crushing the resultant material.

Claims (20)

1. Monodispersed, spherical zirconium oxide nanoparticles approximately 20 nm to approximately 30 nm in diameter, which exhibit metastable tetragonal crystal structure at room temperature, wherein said particles are approximately 100% in the tetragonal state, and are composed of a single, pure zirconium oxide free of doping with other foreign oxides, prepared by a process comprising the steps of:

preparing equal parts of an alcohol solution wherein a first part is mixed with deionized water and a second part is mixed with a zirconium-alkoxide under processing conditions using an R-value of 60, wherein the R-value comprises the ratio of molar concentration of water to zirconium-alkoxide;

adding a polymeric steric stabilizer to the first part of an alcohol solution with deionized water, wherein the stabilizer is in a concentration of approximately 1.0 to approximately 2.0 g/L and stirring until homogenized and forming a solution one;

dissolving the zirconium alkoxide in the second part of the alcohol solution and forming a solution two;

mixing the solution one and the solution two together;

stirring the mixture for approximately 4 hours;

holding the stirred mixture under static conditions for approximately 24 hours to complete the hydrolysis and condensation reactions;

drying at approximately 80 degrees C. to remove solvent and form resultant material;

crushing the resultant material to obtain nanocrystalline ZrO 2 powder, pure and free of foreign oxides, with particle sizes of approximately 20 nm to approximately 30 nm in diameter that form loose agglomerates and exhibit tetragonal crystal structure at room temperature; and

calcining at temperatures ranging from approximately 400° C. to approximately 800° C. wherein the nanocrystalline ZrO 2 powder, pure and free of foreign oxides, with particle sizes of approximately 20 nm to approximately 30 nm in diameter that exhibits tetragonal crystal structure at room temperature then undergoes a gradual transformation from tetragonal to monoclinic phase with an increase in calcination temperature from approximately 400 to approximately 800 degrees C.

2. Monodispersed, spherical zirconium oxide submicron size particles approximately 500 nm to approximately 600 nm in diameter, which exhibit a metastable tetragonal crystal structure at room temperature, wherein said particles are approximately 100% in the tetragonal state, and are composed of a single, pure zirconium oxide, free of doping with other foreign oxides, prepared by a process comprising the steps of:

preparing equal parts of an alcohol solution wherein a first part is mixed with deionized water and a second part is mixed with a zirconium-alkoxide under processing conditions using an R-value of 5, wherein the R-value comprises the ratio of molar concentration of water to zirconium-alkoxide;

adding a polymeric steric stabilizer to the first part of an alcohol solution with deionized water, wherein the stabilizer is in a concentration of approximately 1.0 to approximately 2.0 g/L and stirring until homogenized and forming a solution one;

dissolving the zirconium alkoxide in the second part of the alcohol solution and forming a solution two;

mixing the solution one and the solution two together;

stirring the mixture for approximately 4 hours;

holding the stirred mixture under static conditions for approximately 24 hours to complete the hydrolysis and condensation reactions;

drying at approximately 80 degrees C. to remove solvent and form resultant material;

crushing the resultant material to obtain submicron sized ZrO 2 particles, pure and free of foreign oxides, with particle sizes of approximately 500 nm to approximately 600 nm in diameter that form hard aggregates and exhibit tetragonal crystal structure at room temperature; and

calcining at temperatures ranging from approximately 400° C. to approximately 600° C. wherein the submicron sized ZrO 2 particles, pure and free of foreign oxides, with particle sizes of approximately 500 nm to approximately 600 nm in diameter exhibit a metastable tetragonal phase between approximately 400° C. to approximately 600° C. and with an increase in calcination temperature to approximately 800 degrees C., transformation from tetragonal to monoclinic phase occurs.

Continuity (3)
Division 1065598600 · Sep 5, 2003
Provisional Application 6040832500 · Sep 5, 2002
Related Publication 20080050307A1 · Feb 28, 2008