Method for manufacturing ceramic honeycombs with reduced shrinkage

Patent metadata

Field	Value
Publication number	US-9464004-B2
Application number	US-201113036596-A
Country	US
Kind code	B2
Filing date	Feb 28, 2011
Priority date	Feb 28, 2011
Publication date	Oct 11, 2016
Grant date	Oct 11, 2016

Abstract

A method of manufacturing porous ceramic articles is provided that includes forming a plurality of extruded green bodies from a ceramic precursor batch composition. The method also includes firing the extruded green bodies in a tunnel kiln to produce porous ceramic articles, periodically determining a shrinkage characteristic of at least one sample passing through the tunnel kiln, and adjusting a top soak temperature in the kiln if the shrinkage characteristic is outside of a predetermined range.

First claim

What is claimed is:

1. A method of manufacturing porous ceramic articles, comprising:
a) forming a plurality of extruded green bodies from a ceramic precursor batch composition comprising a particle size distribution (PSD) defined by a mixture of raw materials used to form the ceramic batch precursor composition, wherein a target PSD is determined to results in a firing shrinkage of a porous ceramic article to a target specification dimension, and wherein the PSD changes from the target PSD;
b) firing the extruded green bodies in a tunnel kiln comprising a zone through which each of the extruded green bodies pass, wherein the zone is heated to a top soak temperature to produce from each extruded green body a porous ceramic article that undergoes an amount of shrinkage or growth variability during said firing, wherein the amount of shrinkage or growth variability is defined by a shrinkage characteristic, and wherein the porous ceramic article has a porosity, a pore diameter, a coefficient of thermal expansion and a modulus of rupture;
c) determining the shrinkage characteristic of at least one sample of the porous ceramic articles formed by said firing wherein the shrinkage characteristic is the amount of shrinkage or growth variability being a dimensional change of the porous ceramic article away from the target specification as caused by the change in the PSD of the ceramic batch precursor composition; and
d) wherein, whenever the amount of shrinkage or growth variability as caused by the change in the PSD of the ceramic batch precursor composition is at least 0.2% above or at least 0.2% below the target specification: adjusting the top soak temperature based on the determined shrinkage characteristic to cause a change in the shrinkage characteristic of subsequently formed porous ceramic articles that reduces the amount of shrinkage or growth variability for each porous ceramic article; and
e) wherein the adjusting of the top soak temperature includes either:
i) a downward adjustment of between 5° C. and 10° C. from a predetermined top soak temperature for every 0.2% that the determined shrinkage characteristic is above the target specification; or
ii) an upward adjustment of between 5° C. and 10° C. from a predetermined top soak temperature for every 0.2% that the determined shrinkage characteristic is below the target specification.

2. The method of claim 1 , wherein the extruded green bodies and porous ceramic articles have a circular, elliptical or asymmetrical shape cross-section and the determining of the shrinkage characteristic comprises measuring a length of a major cross-sectional axis of the at least one sample as an extruded green body and as a porous ceramic article.

3. The method of claim 1 , wherein the extruded green bodies and porous ceramic articles have an axial length and wherein the determining of the shrinkage characteristic comprises measuring the axial length of the at least one sample as an extruded green body and as a porous ceramic article.

4. The method of claim 1 , wherein the top soak temperature is adjusted downward when the determined shrinkage characteristic is above a predetermined amount.

5. The method of claim 4 , wherein the top soak temperature is adjusted downward at least 7° C. from a predetermined top soak temperature for every 0.2% that the determined shrinkage characteristic is above a predetermined set point.

6. The method of claim 1 , wherein the top soak temperature is adjusted upward at least 7° C. from a predetermined top soak temperature for every 0.2% that the determined shrinkage characteristic is below a predetermined set point.

7. The method of claim 1 , wherein the determined shrinkage characteristic is measured for at least 1 out of every 1000 of the extruded green bodies formed in act a).

8. The method of claim 1 , wherein the adjusting of the top soak temperature occurs before the subsequently formed ceramic articles enter the zone heated to the top soak temperature.

9. The method of claim 8 , wherein the adjusting of the top soak temperature is performed within 5 hours of the subsequently formed ceramic articles entering the zone heated to the top soak temperature.

10. The method of claim 1 , wherein the extruded green bodies are passed into the tunnel kiln in a plurality of vehicles traveling sequentially through the tunnel kiln and a plurality of extruded green bodies are placed on each vehicle.

11. The method of claim 1 , wherein the top soak zone comprises a plurality of sub-zones that can each be individually heated to different temperatures than other sub-zones.

12. The method of claim 11 , wherein, if the shrinkage characteristic is outside of a predetermined range, the top soak temperature is adjusted by changing the temperature of all of the sub-zones.

13. The method of claim 11 , wherein, when the shrinkage characteristic is outside of a predetermined range, the top soak temperature is adjusted by changing the temperature in only some of the sub-zones.

14. The method of claim 11 , wherein, when the shrinkage characteristic is outside of a predetermined range, the top soak temperature is adjusted by changing the temperature in at least one sub-zone sequentially as the subsequently formed ceramic articles-pass through the zone heated to the top soak temperature.

15. The method of claim 1 , wherein the ceramic precursor batch composition comprises cordierite-forming ingredients.

16. The method of claim 1 , wherein the ceramic precursor batch composition comprises aluminum titanate-forming ingredients.

17. The method of claim 1 , wherein the top soak temperature ranges from 1380° C. to 1450° C.

18. The method of claim 1 , wherein the change in the PSD of the ceramic batch precursor composition is caused by a change in a PSD of at least one of the raw materials.

Assignees

• Balster Jean E
• Brown Michael P
• Deneka Thomas James
• Howell Joshua L
• Mccauley Daniel Edward
• Corning Inc

Inventors

• Balster Jean E
• Brown Michael P
• Deneka Thomas James
• Howell Joshua L
• Mccauley Daniel Edward

Classifications

• C04B35/195 Primary

  Alkaline earth aluminosilicates, e.g. cordierite {or anorthite} · CPC title

• B28B17/0072

  Product control or inspection · CPC title

• C04B35/478

  based on aluminium titanates · CPC title

• F27B9/30

  Details, accessories or equipment specially adapted for furnaces of these types · CPC title

• C04B2235/9615

  Linear firing shrinkage · CPC title