Ammonia oxidation/decomposition catalyst
Provided is an ammonia oxidation/decomposition catalyst which can decrease the reduction temperature of a support, which is required for the catalyst to have a property of being activated at room temperature, and also can render a property of being activated at a temperature lower than room temperature. The ammonia oxidation/decomposition catalyst of the present invention is an ammonia oxidation/decomposition catalyst, comprising: a catalyst support composed of a composite oxide of cerium oxide and zirconium oxide; and at least one metal selected from the group consisting of metals of group 6A, group 7A, group 8, and group 1B as a catalytically active metal deposited thereon, characterized in that the molar concentration of zirconium oxide in the catalyst support is from 10 to 90%.
1. A method for activating an ammonia oxidation/decomposition catalyst comprising:
providing the ammonia oxidation/decomposition catalyst comprising a catalyst support composed of composite oxide of cerium oxide and zirconium oxide and a catalytically active metal deposited thereon, wherein the molar concentration of zirconium oxide in the catalyst support is from 10 to 90%;
heating the catalyst at 200 to 400° C. in a hydrogen stream or in an ammonia stream in order to reduce a part of or the whole of the cerium oxide constituting the catalyst support to
CeO 2-x (0< x< 2); and
then supplying oxygen and ammonia simultaneously to the catalyst at a temperature between room temperature and −30° C. in order to generate oxidation heat by the reaction of the catalyst support in a reduced state with oxygen such that the temperature of the catalyst layer is increased to a temperature at which ammonia and oxygen are reacted with each other.
2. The method according to claim 1 , wherein the catalyst support is in a honeycomb form.
3. The method according to claim 1 , wherein the catalyst support is in a pellet form.
4. The method according to claim 1 , wherein the molar concentration of the zirconium oxide in the catalyst support is from 20% to 70%.
5. The method according to claim 1 , wherein the catalytically active metals is at least one metal selected from the group consisting of metals from groups 6A, 7A, 8 and 1B.