US2016279611A1PendingUtilityA1
Catalyst with lanthamide-doped zirconia and methods of making
Est. expiryAug 10, 2031(~5.1 yrs left)· nominal 20-yr term from priority
C01F 17/32C01P 2002/72C04B 2235/3205B01J 37/0244C04B 35/50C01P 2002/54C04B 2235/3229B01J 37/0201C01G 25/02B01J 37/0236C04B 2235/3227C04B 35/486B01J 37/038C04B 2235/3224B01J 2523/00C01P 2002/52B01J 37/0036B01J 23/002C04B 35/488B01J 23/10B01J 23/464B01J 23/63C01G 25/00B01J 2235/00B01J 2235/15B01J 35/70B01J 35/0006B01J 35/02B01J 35/19
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Claims
Abstract
The invention generally relates to three-way catalysts and catalyst formulations capable of simultaneously converting nitrogen oxides, carbon monoxide, and hydrocarbons into less toxic compounds. Such three-way catalyst formulations contain ZrO 2 -based mixed-metal oxide support oxides doped with an amount of lanthanide. Three-way catalyst formulations with the support oxides of the present invention demonstrate higher catalytic activity, efficiency and longevity than comparable catalysts formulated with traditional support oxides.
Claims
exact text as granted — not AI-modified1 . A support oxide comprising ZrO 2 doped with an amount of lanthanide.
2 . The support oxide of claim 1 , wherein said support oxide further comprises Al 2 O 3 or La—Al 2 O 3 .
3 . The support oxide of claim 1 , wherein said lanthanide is La or Pr.
4 . The support oxide of claim 1 , wherein the ZrO 2 is doped with between about 1-30% of said lanthanide.
5 . The support oxide of claim 4 , wherein the ZrO 2 is doped with between about 5-15% of said lanthanide.
6 . The support oxide of claim 1 , wherein said support oxide comprises La X % Zr (1-X) % O 2 and/or Pr X % Zr (1-X) % O 2 .
7 . The support oxide of claim 6 , wherein said support oxide comprises La 5% Zr 95% O 2 , Pr 5% Zr 95% O 2 , La 10% Zr 90% O 2 , Pr 10% Zr 90% O 2 , La 15% Zr 85% O 2 , Pr 15% Zr 85% O 2 , or mixtures thereof.
8 . The support oxide of claim 1 , wherein said support oxide is in the tetragonal phase.
9 . The support oxide of claim 1 , wherein said support oxide further comprises an oxygen storage material (OSM).
10 . A washcoat or overcoat comprising a support oxide, an oxygen storage material (OSM) and a catalyst, wherein said support oxide is according to claim 1 .
11 . The washcoat or overcoat of claim 10 , wherein said catalyst is a platinum group metal (PGM) catalyst.
12 . The washcoat or overcoat of claim 11 , wherein said PGM is Rh, Pt, Pd, or a mixture thereof.
13 . The washcoat or overcoat of claim 12 , wherein said PGM is Rh.
14 . The washcoat or overcoat of claim 13 , wherein said Rh is present at 0.25% (by weight) of said washcoat.
15 . The washcoat or overcoat of claim 10 , wherein said support oxide constitutes 1-100% (by weight) of said washcoat or overcoat.
16 . A washcoat or overcoat comprising:
a) (i) 40% oxygen storage material (OSM); (ii) 30% Al 2 O 3 or La—Al 2 O 3 ; and (iii) 30% Pr 0.05 Zr 0.95 O 2 ; b) (i) 40% OSM; (ii) 30% Al 2 O 3 or La—Al 2 O 3 ; and (iii) 30% La 0.05 Zr 0.95 O 2 ; c) (i) 40% OSM; 30% Al 2 O 3 or La—Al 2 O 3 ; and (iii) 30% Pr 0.10 Zr 0.90 O 2 ; d) (i) 40% OSM; 30% Al 2 O 3 or La—Al 2 O 3 ; and (iii) 30% La 0.10 Zr 0.90 O 2 ; e) (i) 40% OSM; 30% Al 2 O 3 or La—Al 2 O 3 ; and (iii) 30% Pr 0.15 Zr 0.85 O 2 ; f) (i) 40% OSM; 30% Al 2 O 3 or La—Al 2 O 3 ; and (iii) 30% La 0.15 Zr 0.85 O 2 ; g) (i) 40% OSM; and (ii) 60% Pr 0.05 Zr 0.95 O 2 ; h) (i) 40% OSM; and (ii) 60% La 0.05 Zr 0.95 O 2 ; i) (i) 40% OSM; and (ii) 60% Pr 0.10 Zr 0.90 O 2 ; j) (i) 40% OSM; and (ii) 60% La 0.10 Zr 0.90 O 2 ; k) (i) 40% OSM; and (ii) 60% Pr 0.15 Zr 0.85 O 2 ; or l) (i) 40% OSM; and (ii) 60% La 0.15 Zr 0.85 O 2 .
17 . A washcoat or overcoat according to claim 15 , wherein said OSM is:
Ce 1-a-b-c-d D a E b F c Zr d O 2 ,
wherein:
a, b and c are, independently, 0-0.7;
d is 0-0.9; and
D, E and F are, independently, selected from the group consisting of lanthanides, alkaline earth metals and transition metals.
18 . A washcoat or overcoat according to claim 17 , wherein said OSM is Ce 0.3 Nd 0.05 Pr 0.05 Zr 0.6 O 2 .
19 . A catalyst system comprising: a substrate and a washcoat,
wherein said washcoat is according to claim 10 .
20 . A catalyst system comprising: a substrate, a washcoat, and an overcoat,
wherein said washcoat is according to claim 10 ; and said overcoat comprises a support oxide, an oxygen storage material (OSM), and a catalyst.
21 . A catalyst system comprising: a substrate, a washcoat, and an overcoat,
wherein said washcoat comprises a support oxide, an oxygen storage material (OSM) and a catalyst; and wherein said overcoat is according to claim 10 .
22 . The catalyst system of claim 21 , wherein said catalyst in said overcoat is a platinum group metal (PGM) catalyst.
23 . The catalyst system of claim 22 , wherein said catalyst in said overcoat is Rh, Pt, Pd, or a mixture thereof.
24 . The catalyst system of claim 23 , wherein said catalyst in said overcoat is Pd.
25 . The catalyst system of claim 24 , wherein said Pd is present at 100 g/ft 3 .
26 . The catalyst system of claim 21 , wherein said catalyst in said washcoat is a platinum group metal (PGM) catalyst.
27 . The catalyst system of claim 26 , wherein said catalyst in said washcoat is Rh, Pt, Pd, or a mixture thereof.
28 . The catalyst system of claim 27 , wherein said catalyst in said washcoat is Pd.
29 . The catalyst of claim 28 , wherein said Pd is present at 100 g/ft 3 .
30 . The catalyst system of claim 19 , wherein said catalyst system is a three way conversion catalyst system.
31 . The catalyst system of claim 19 , wherein said catalyst system exhibits improved gas flow when compared to catalyst systems comprising only traditional support oxides.
32 . The catalyst system of claim 19 , wherein said catalyst system exhibits improved light-off performance when compared to catalyst systems comprising only traditional support oxides.
33 . A method of making a catalyst system comprising:
a) depositing a washcoat according to claim 10 on a substrate; b) treating said washcoat and substrate by calcination; and c) optionally impregnating a platinum group metal (PGM) catalyst into said washcoat, followed by drying and calcination.
34 . A method of making a catalyst system comprising:
a) depositing a washcoat according to claim 10 on a substrate; b) treating said washcoat and substrate by calcination; c) optionally impregnating a platinum group metal (PGM) catalyst into said washcoat, followed by drying and calcination; d) depositing an overcoat onto the washcoat;
wherein said overcoat comprises a support oxide, an oxygen storage material and a catalyst;
e) optionally impregnating a PGM catalyst into said overcoat, followed by drying and calcination.
35 . A method of making a catalyst system comprising:
a) depositing a washcoat on a substrate,
wherein said washcoat comprises a support oxide, an oxygen storage material and a catalyst;
b) treating said washcoat and substrate by calcination; c) optionally impregnating a platinum group metal (PGM) catalyst into said washcoat, followed by drying and calcination; d) depositing an overcoat according to claim 10 onto the washcoat; e) optionally impregnating a PGM catalyst into said overcoat, followed by drying and calcination.
36 . (canceled)
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