Soda-lime-silica glass-ceramic

Patent metadata

Field	Value
Publication number	US-10273183-B2
Application number	US-201715650441-A
Country	US
Kind code	B2
Filing date	Jul 14, 2017
Priority date	Jul 14, 2017
Publication date	Apr 30, 2019
Grant date	Apr 30, 2019

Abstract

A soda-lime-silica glass-ceramic article having an amorphous matrix phase and a crystalline phase is disclosed along with a method of manufacturing a soda-lime-silica glass-ceramic article from a parent glass composition comprising 47-63 mol % SiO2, 15-22 mol % Na2O, and 18-36 mol % CaO. The crystalline phase of the glass-ceramic article has a higher concentration of sodium (Na) than that of the amorphous matrix phase.

First claim

The invention claimed is:

1. A method of manufacturing a soda-lime-silica glass-ceramic container comprising:
forming a glass body from a parent glass composition comprising 47-63 mol % SiO 2 , 15-22 mol % Na 2 O, and 18-36 mol % CaO, the glass body being in the shape of a container; and
subjecting the glass body to a thermal treatment schedule to promote bulk in situ crystallization of the glass body such that the glass body is transformed into a glass-ceramic body having an amorphous matrix phase and a crystalline phase homogeneously dispersed throughout the amorphous matrix phase, the crystalline phase comprising combeite crystalline particles.

2. The method set forth in claim 1 , wherein the thermal treatment schedule comprises:
a nucleation stage wherein the glass body is brought to a temperature in a range of 525° C.-625° C. and maintained within the range of 525° C.-625° C. for 10 minutes to 180 minutes such that a plurality of nuclei spontaneously form within the glass body; and
a crystal growth stage wherein the glass body is brought to a temperature in a range of 600° C.-750° C. and maintained within the range of 600° C.-750° C. for 10 minutes to 120 minutes such that a plurality of crystalline particles form on the pre-existing nuclei.

3. The method set forth in claim 1 , wherein, during the crystal growth stage, the glass body is maintained at a temperature in a range of 600° C.-750° C. for an amount of time to transform the glass body into a glass-ceramic body having a crystalline volume fraction in the range of 0.10 to 0.70.

4. A method of manufacturing a soda-lime-silica glass-ceramic container comprising:
forming a glass body from a parent glass composition comprising 47-63 mol % SiO 2 , 15-22 mol % Na 2 O, and 18-36 mol % CaO, the glass body being in the shape of a container; and
subjecting the glass body to a thermal treatment schedule to promote bulk in situ crystallization of the glass body such that the glass body is transformed into a glass-ceramic body having an amorphous matrix phase and a crystalline phase homogeneously dispersed throughout the amorphous matrix phase, wherein the glass body is not cooled to a temperature below a glass transition temperature of the parent glass composition prior to being subjected to the thermal treatment schedule.

5. The method set forth in claim 1 , wherein the thermal treatment schedule comprises:
a combined nucleation and crystal growth stage, wherein the glass body is brought to a temperature in a range of 600° C.-750° C. and maintained within said range for 10 minutes to 180 minutes.

6. The method set forth in claim 1 , wherein the thermal treatment schedule comprises:
an annealing stage, wherein the glass-ceramic body is gradually cooled to a temperature below a strain point of the amorphous matrix phase to reduce internal stresses within the glass-ceramic body.

7. A method of manufacturing a soda-lime-silica glass-ceramic container comprising:
forming a glass body from a parent glass composition comprising 47-63 mol % SiO 2 , 15-22 mol % Na 2 O, and 18-36 mol % CaO, the glass body being in the shape of a container;
maintaining the glass body at a temperature between 525° C. and 600° C. to form nuclei spontaneously and homogeneously throughout the glass body;
maintaining the glass body at a temperature between 600° C. and 750° C. to grow crystals on the nuclei throughout the glass body and thereby transform the glass body into a glass-ceramic body; and
annealing the glass-ceramic body at a temperature between 540° C. and 580° C. followed by cooling the glass-ceramic body to a temperature below a strain point of the amorphous glass matrix of the glass-ceramic body to reduce internal stresses within the glass-ceramic body.

8. The method set forth in claim 7 , wherein the glass body is not cooled to a temperature below the glass transition temperature of the parent glass composition prior to maintaining the glass body at a temperature between 525° C. and 600° C. to form nuclei spontaneously and homogeneously throughout the glass body.

9. The method set forth in claim 7 , wherein the glass-ceramic body comprises combeite crystalline particles homogeneously dispersed within an amorphous glass matrix, and wherein the glass-ceramic body does not include particles of devitrite (Na 2 O.3CaO.6SiO 2 ), wollastonite (CaO.SiO 2 ), or a SiO 2 polymorph.

10. The method set forth in claim 7 , wherein the glass body is maintained at a temperature between 580° C. and 610° C. to form nuclei, and wherein the glass body is further maintained at a temperature between 680° C. and 730° C. to grow crystals on the nuclei.

Assignees

• Owens Brockway Glass Container

Inventors

• Cooper Scott P
• Schuver Samuel
• Click Carol A

Classifications

• C03C3/087

  containing calcium oxide, e.g. common sheet or container glass · CPC title

• C03C10/0009 Primary

  containing silica as main constituent · CPC title

• B65D1/0207

  characterised by material, e.g. composition, physical features · CPC title

• C03C4/20

  for chemical resistant glass · CPC title

• C03C3/078

  containing an oxide of a divalent metal, e.g. an oxide of zinc · CPC title