Systems and Methods Using Cu-Mn Spinel Catalyst on Varying Carrier Material Oxides for TWC Applications
Disclosed here are variations of carrier material oxide formulations to create Cu—Mn spinel, where the formulations may include Ti 1-x Nb x O 2 , TiO 2 , SiO 2 , Doped alumina, Nb 2 O 5 —ZrO 2 , Nb 2 O 5 —ZrO 2 —CeO 2 , Doped ZrO 2 and combinations thereof. The formation of type of Cu—Mn oxide phase depends on type of carrier material oxide. The crystallite size of Cu—Mn spinel, NO and CO conversion rate of Cu—Mn Spinel may vary according to the carrier material oxide and condition treatment used to form the spinel during co-precipitation method.
1 . A zero platinum group metals (ZPGM) catalyst system, comprising:
a substrate;
a washcoat suitable for deposition on the substrate, comprising at least one oxide solid selected from the group consisting of at least one of a carrier material oxide, and a first ZPGM catalyst; and
an overcoat suitable for deposition on the substrate, comprising at least one overcoat oxide solid selected from the group consisting of at least one of a carrier material oxide, and a second ZPGM catalyst;
wherein at least one of the first catalyst and the second catalyst comprises at least one spinel structured compound having the formula AB 2 O 4 , wherein each of A and B is selected from the group consisting of at least one of copper and manganese; and
wherein one of the at least one carrier material oxide in selected from the group consisting of TiO 2 , doped TiO 2 , Ti1-xNbxO 2 , SiO 2 , alumina, doped alumina, ZrO 2 , doped ZrO 2 , Nb 2 O 5 —ZrO 2 , Nb 2 O 5 —ZrO 2 —CeO 2 , and combinations thereof.
2 . The ZPGM catalyst system of claim 1 , wherein the substrate comprises cordierite.
3 . The ZPGM catalyst system of claim 1 , wherein the spinel structured compound is prepared by co-precipitation.
4 . The ZPGM catalyst system of claim 3 , wherein a metal salt solution is used in the co-precipitation process and is selected from the group consisting of copper nitrate, copper acetate, manganese nitrate, manganese acetate, and combinations thereof.
5 . The ZPGM catalyst system of claim 1 , wherein the crystallite size of the spinel structured compound is dependent on the carrier material oxide.
6 . The ZPGM catalyst system of claim 5 , wherein the crystallite size of the spinel structured compound is about 18 nm.
7 . The ZPGM catalyst system of claim 5 , wherein the crystallite size of the spinel structured compound is about 8 nm.
8 . The ZPGM catalyst system of claim 1 , wherein the spinel structured compound is aged.
9 . The ZPGM catalyst system of claim 8 , wherein the spinel structured compound is stable.
10 . The ZPGM catalyst system of claim 1 , wherein the phase of the spinel structured compound is dependent on the carrier material oxide.
11 . The ZPGM catalyst system of claim 1 , wherein an NO conversion rate corresponds to the carrier material oxide.
12 . The ZPGM catalyst system of claim 1 , wherein a T50 conversion temperature for carbon monoxide is less than about 200 degrees Celsius.
13 . The ZPGM catalyst system of claim 1 , wherein a T50 conversion temperature for carbon monoxide is less than about 175 degrees Celsius.
14 . The ZPGM catalyst system of claim 1 , wherein the at least one carrier material oxide comprises Nb 2 O 5 —ZrO 2 .
15 . The ZPGM catalyst system of claim 14 , wherein the ZrO 2 is about 60% to about 80% by weight of the at least one carrier material oxide.
16 . The ZPGM catalyst system of claim 14 , wherein the ZrO 2 is about 75% by weight of the at least one carrier material oxide.
17 . The ZPGM catalyst system of claim 1 , wherein the at least one carrier material oxide is heated to about 900° C. for about 4 hours.
18 . The ZPGM catalyst system of claim 1 , wherein the doped ZrO 2 comprises praseodymium.
19 . The ZPGM catalyst system of claim 18 , wherein the ZrO 2 is about 80% to about 95% by weight of the at least one carrier material oxide.
20 . The ZPGM catalyst system of claim 18 , wherein the ZrO is about 90% by weight of the at least one carrier material oxide.