Bimetallic synergized PGM catalyst systems for TWC application
Bimetallic Synergized Platinum Group Metals (SPGM) catalyst systems for TWC application are disclosed. Disclosed bimetallic SPGM catalyst systems may include a washcoat with a Cu—Mn spinel structure and an overcoat that includes PGMs, such as Pd/Rh or Pt/Rh supported on carrier material oxides, such as alumina. Bimetallic SPGM catalyst systems show significant improvement in nitrogen oxide reduction performance under lean operating conditions, which allows a reduced consumption of fuel. Additionally, disclosed bimetallic SPGM catalyst systems exhibit enhanced catalytic activity for carbon monoxide conversion. Furthermore, bimetallic SPGM catalyst systems are found to have enhanced catalytic activity for fresh, hydrothermally aged and fuel cut aged conditions compared to PGM catalyst system, showing that there is a synergistic effect between PGM catalyst and Cu—Mn spinel within the disclosed SPGM catalyst system which help in performance and thermal stability of disclosed SPGM catalyst systems.
1. A bimetallic synergized platinum group metals (SPGM) catalyst system comprising:
a) an overcoat comprising a bimetallic PGM catalyst;
b) a washcoat comprising a Cu—Mn spinel supported on doped ZrO 2 support oxide; and
c) a substrate.
2. The bimetallic SPGM catalyst system of claim 1 , wherein the substrate comprises a ceramic material.
3. The bimetallic SPGM catalyst system of claim 2 , wherein the bimetallic PGM catalyst is supported on a carrier material oxide.
4. The bimetallic SPGM catalyst system of claim 3 , wherein the carrier material oxide is Al 2 O 3 .
5. The bimetallic SPGM catalyst system of claim 3 , wherein the carrier material oxide is selected from the group consisting of aluminum oxide, doped aluminum oxide, zirconium oxide, doped zirconia, titanium oxide, tin oxide, silicon dioxide, zeolite, and mixtures thereof.
6. The bimetallic SPGM catalyst system of claim 1 , wherein the bimetallic PGM catalyst is palladium/rhodium or platinum/rhodium.
7. The bimetallic SPGM catalyst system of claim 1 , wherein the bimetallic PGM catalyst comprises about 0.5 g/ft 3 of each metal.
8. The bimetallic SPGM catalyst system of claim 1 , wherein the doped ZrO 2 support oxide is Nb 2 O 5 —ZrO 2 .
9. The bimetallic SPGM catalyst system of claim 1 , wherein the Cu—Mn spinel is CuMn 2 O 4 .
10. The bimetallic SPGM catalyst system comprising of claim 1 , wherein:
a) the overcoat comprises a palladium-rhodium catalyst supported on alumina;
b) a washcoat comprises a CuMn 2 O 4 spinel supported on doped ZrO 2 ; and
c) the substrate is a ceramic substrate.
11. The bimetallic SPGM catalyst system of claim 10 , wherein the SPGM catalyst system converts about 92.8% of nitrogen oxide under lean condition.
12. The bimetallic SPGM catalyst system comprising of claim 10 , wherein the SPGM catalyst system converts about 81.5% of carbon monoxide under rich condition.
13. The bimetallic SPGM catalyst system comprising of claim 1 , wherein:
a) the overcoat comprises a platinum-rhodium catalyst supported on alumina;
b) the washcoat comprises of CuMn 2 O 4 spinel supported on doped ZrO 2 ; and
c) the substrate is a ceramic substrate.
14. The bimetallic SPGM catalyst system comprising of claim 13 , wherein the SPGM catalyst system converts about 100% of nitrogen oxide under lease condition.
15. The bimetallic SPGM catalyst system comprising of claim 1 , wherein the SPGM catalyst system is hydrothermally aged.
16. The bimetallic SPGM catalyst system comprising of claim 15 , wherein the hydrothermal aging is an aging treatment of 900° C. for about 4 hours.
17. A method of converting nitrogen oxide and carbon monoxide comprising applying exhaust gas to a bimetallic synergized platinum group metals (SPGM) catalyst system comprising:
a) an overcoat comprising a bimetallic PGM catalyst;
b) a washcoat comprising a Cu—Mn spinel supported on doped ZrO 2 support oxide; and
c) a substrate.
18. The method of claim 17 , wherein the substrate comprises a ceramic material.
19. The method of claim 18 , wherein the bimetallic PGM catalyst is supported on a carrier material oxide.
20. The method of claim 19 , wherein the carrier material oxide is Al 2 O 3 .
21. The method of claim 19 , wherein the carrier material oxide is selected from the group consisting of aluminum oxide, doped aluminum oxide, zirconium oxide, doped zirconia, titanium oxide, tin oxide, silicon dioxide, zeolite, and mixtures thereof.
22. The method of claim 17 , wherein the bimetallic PGM catalyst is palladium/rhodium or platinum/rhodium.
23. The method of claim 17 , wherein the bimetallic PGM catalyst comprises about 0.5 g/ft 3 of each metal.
24. The method of claim 17 , wherein the doped ZrO 2 support oxide is Nb 2 O 5 —ZrO 2 .
25. The method of claim 17 , wherein the Cu—Mn spinel is CuMn 2 O 4 .
26. The method of claim 17 , wherein:
a) the overcoat comprises a palladium-rhodium catalyst supported on alumina;
b) a washcoat comprises a CuMn 2 O 4 spinel supported on doped ZrO 2 ; and
c) the substrate is a ceramic substrate.
27. The method of claim 26 , wherein the SPGM catalyst system converts about 92.8% of nitrogen oxide under lean condition.
28. The method of claim 26 , wherein the SPGM catalyst system converts about 81.5% of carbon monoxide under rich condition.
29. The method of claim 17 , wherein:
a) the overcoat comprises a platinum-rhodium catalyst supported on alumina;
b) the washcoat comprises of CuMn 2 O 4 spinel supported on doped ZrO 2 ; and
c) the substrate is a ceramic substrate.
30. The method of claim 29 , wherein the SPGM catalyst system converts about 100% of nitrogen oxide under lease condition.
31. The method of claim 17 , wherein the SPGM catalyst system is hydrothermally aged.
32. The method of claim 31 , wherein the hydrothermal aging is an aging treatment of 900° C. for about 4 hours.