Granted Patent B2

US 7,832,233 · App. 11/131,919 · Granted Nov 16, 2010

Abstract

Claims (56)

1. A method of forming a decorated glass structure comprising:

a. applying to a first glass substrate a green crystallizing enamel composition comprising, prior to firing:

i. a reactive glass component,

ii. an oxidizer component comprising at least two oxidizers selected from the group consisting of ammonium nitrate, antimony pentoxide, barium nitrate, bismuth pentoxide, bismuth oxynitrate, bismuth tetroxide, calcium nitrate, calcium peroxide, cesium nitrate, cobalt nitrate, copper nitrate, lithium nitrate, magnesium peroxide, manganese dioxide, nickel (III) oxide, platinum monoxide, platinum dioxide, potassium nitrate, potassium peroxide, sodium nitrate, sodium percarbonate, sodium peroxide, strontium nitrate, strontium peroxide, silver nitrate, tellurium trioxide, tin nitrate, and zinc peroxide and combinations thereof,

iii. a pigment,

iv. an organic vehicle comprising a binder and a solvent, and

v. a seed material selected from the group consisting of Zn 2 SiO 4 , Bi 12 SiO 20 , Bi 4 (SiO 4 ) 3 , Bi 2 SiO 5 , 2ZnO.3TiO 2 , Bi 2 O 3 .SiO 2 , Bi 2 O 3 .2TiO 2 , 2Bi 2 O 3 .3TiO 2 , Bi 7 Ti 4 NbO 21 , Bi 4 Ti 3 O 12 , Bi 2 Ti 2 O 7 , Bi 12 TiO 20 , Bi 4 Ti 3 O 12 , Bi 2 Ti 4 O 11 , and combinations thereof, wherein the green ceramic enamel composition is substantially free of silica gels,

b. stacking a second glass substrate with the first glass substrate wherein the green crystallizing enamel composition lies between the first and second glass substrates, and

c. subjecting the stacked glass substrates to a firing operation whereby:

i. only the first glass substrate bears a sintered enamel composition,

ii. the organic vehicle burns out completely, and

iii. the glass substrates do not stick to one another.

2. The method of claim 1 wherein the crystallizing enamel composition comprises:

a. 20-80 wt % of the glass component,

b. 0.01-7 wt % of the oxidizer component,

c. 10-40% of the pigment, and

d. 10-40 wt % of the organic vehicle.

3. The method of claim 2 wherein the oxidizer component comprises an oxidizer selected from the group consisting of ammonium nitrate, bismuth oxynitrate, sodium nitrate, and manganese dioxide and combinations thereof.

4. The method of claim 1 wherein the oxidizer component comprises bismuth oxynitrate and manganese dioxide in a weight ratio of about 1:2 to about 2:1.

5. The method of claim 1 wherein the oxidizer component comprises manganese dioxide and sodium nitrate in a weight ratio of about 15:1 to about 2:1.

6. The method of claim 1 wherein the reactive glass component comprises at least one frit, wherein the at least one frit is selected from the group consisting of bismuth borosilicate fit, zinc borosilicate frit, and combinations thereof, wherein:

a. the bismuth borosilicate frit comprises

i. 9-75 wt % Bi 2 O 3 ,

ii. 0.1-28 wt % SiO 2 , and

iii. 0.1-9 wt % B 2 O 3 ,

b. the zinc borosilicate fit comprises

i. 21-50 wt % ZnO 2 ,

ii. 0.1-28 wt % SiO 2 , and

iii. 21-60 wt % B 2 O 3 .

7. The method of claim 1 wherein the glass component comprises:

a. 15-60 wt % Bi 2 O 3 ,

b. 5-50 wt % SiO 2 ,

c. 1-20 wt % B 2 O 3 , and

d. 5-50 wt % ZnO 2 .

8. The method of claim 1 wherein the organic vehicle comprises:

a. a binder selected from the group consisting of methyl cellulose, ethyl cellulose, and hydroxypropyl cellulose, and combinations thereof, and

b. a solvent selected from the group consisting of diethylene glycol butyl ether; 2,2,4-trimethyl pentanediol monoisobutyrate; alpha-terpineol; beta-terpineol; gamma terpineol; tridecyl alcohol; diethylene glycol ethyl ether, diethylene glycol dibutyl ether; and blends thereof.

9. The method of claim 8 wherein the solvent and the binder are present in a weight ratio of about 50:1 to about 20:1.

10. The method of claim 1 wherein the firing operation is conducted at a temperature within the range of about 500° C. to about 750° C.

11. The method of claim 1 wherein the crystallizing enamel composition comprises, prior to firing:

a. 20-80 wt % of the reactive glass component, wherein the reactive glass component includes one selected from the group consisting of reactive oxide-frit, reactive sulfide-frit and combinations thereof, having a melting point of about 450° C. to about 550° C.,

b. 0.1-7 wt % of the oxidizer component, wherein the oxidizer component comprises at least one of the following:

i. bismuth oxynitrate having a D 50 within the range of 8-13 microns,

ii. manganese dioxide having a D 50 within the range of 1-5 microns,

iii. ammonium nitrate, and

iv. sodium nitrate,

c. 10-30 wt % of the pigment

d. 1-5 wt % of a bismuth containing crystal seed material

e. 0-7 wt % of a zinc containing crystal seed material, and

f. 10-40 wt % of the organic vehicle, wherein the organic vehicle comprises

i. 0.5-5 wt % of ethyl cellulose and

ii. 95-99.5 wt % of diethylene glycol monobutyl ether.

12. The method of claim 11 wherein the crystallizing enamel composition further comprises 10-50 wt % of a reactive frit having a melting point within the range of about 580° C. to about 680° C.

13. The method of claim 11 , further comprising forming the fired glass by a process selected from the group consisting of: (1) subjecting the glass to a forming pressure with a die and separating the formed glass from the die and (2) subjecting the glass to a gravity sag.

14. The method of claim 1 , wherein the oxidizer component comprises bismuth oxynitrate and manganese dioxide.

15. The method of claim 1 , wherein the oxidizer component comprises ammonium nitrate and sodium nitrate.

Assignments (14)