Corning Incorporated

Tonia Havewala Fletcher

Christopher Lee Timmons

Robert John Paisley

David A Earl

Richard Wayne Bernard

Kishor Purushottam Gadkaree

Kenneth Edward Hrdina

Kamjula Pattabhirami Reddy

Christopher John Malarkey

Thomas G Havens

Irene Mona Peterson

Sinue Gomez-Mower

Daniel Arthur Sternquist

Rebecca Lynn Schulz

John Steele Abbott, Jr

John Steele Abbott Jr

Embodiments described herein are directed to compositions, systems, and processes for strengthening glass articles, which also minimize the concentration of decomposition products in the molten salt baths used in ion exchange processes to extend salt bath life and maintain the chemical durability of strengthened glass articles over time. The salt bath compositions may generally include from 90 wt. % to 99.9 wt. % of one or more alkali or metal salts and from 0.1 wt. % to 10 wt. % of silicic acid aggregates based on the total weight of the salt bath composition.

Salt bath compositions, salt bath systems, and processes for strengthening glass articles

An ion exchange tank is provided. The ion exchange tank includes a processing chamber and an additive chamber separated by a weir system, the weir system having a flow channel fluidly connecting the processing chamber to the additive chamber, wherein the flow is divided from the additive chamber by a first partition and divided from the processing chamber by a second partition, wherein the additive chamber comprises a solids-absorbing material disposed therein.

Ion exchange systems and methods for ion exchanging glass articles

A method for forming activated carbon comprises forming a feedstock mixture from a carbon feedstock and a chemical activating agent, and heating the feedstock mixture with microwaves in a plurality of successive heating steps to react the carbon feedstock with the chemical activating agent and form activated carbon. Step-wise heating can be used to efficiently control the microwave activation process.

Microwave energy-assisted, chemical activation of carbon

A cement mixture suitable for use with ceramic honeycomb bodies, such as for forming an outer layer on the outer periphery of the honeycomb body, or for forming plugs in the honeycomb body. The cement mixture, when fired, preferably exhibits low coefficient of thermal expansion and high strength. The cement mixture can be applied to a green honeycomb body and simultaneously fired with the green body or can be applied to an already fired ceramic honeycomb body and then fired. Includes cement mixture comprising a plurality of inorganic components comprising talc, kaolin, alumina, silica, and aluminum hydroxide, wherein the mixture contains less than or equal to 18.0% silica and greater than or equal to 17.0% aluminum hydroxide, in percent by weight of the inorganic components.

Low thermal expansion high strength honeycomb cement and method therefor

Disclosed are cements for ceramic honeycomb bodies. Such cements can be applied to a fired ceramic honeycomb body then fired, or can be applied to an unfired (green) honeycomb body and co-fired with the green honeycomb body. The cement can also be used to plug one or more cells in a honeycomb body, wherein the cement can be inserted into a green or a fired ceramic honeycomb body, then fired. Also disclosed are methods of manufacturing a ceramic honeycomb article with the cement.

Honeycomb cement with ceramic-forming crystallizable glass and method therefor

A method of manufacturing a honeycomb structure is disclosed wherein a green honeycomb body having a first contour is differentially altered such that the green honeycomb body has a second contour which is wider at a first end than at a second end. In one aspect, the altering is accomplished by removing a part of the green honeycomb body, such as with a removal tool. In another aspect, the altering is accomplished by exposing different regions of the honeycomb body to different drying environments.

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Big Flats, NY, United States of America

Tonia Havewala Fletcher