Exhaust treatment device and methods of making the same
An exhaust treatment device comprises a shell; a substrate disposed within the shell, the substrate having a catalyst disposed thereon, wherein the catalyst comprises platinum and a protective layer selected from the group consisting of tin oxide, iron oxide, and manganese oxide, and wherein the catalyst is capable of oxidizing greater than or equal to 50 wt. % carbon monoxide present in an exhaust gas stream at temperatures of about 150° C. to about 200° C.
1 . An exhaust treatment device comprising:
a shell;
a substrate disposed within the shell, the substrate having a catalyst disposed thereon, wherein the catalyst comprises platinum and a protective layer selected from the group consisting of tin oxide, iron oxide, and manganese oxide, and wherein the catalyst is capable of oxidizing greater than or equal to 50 wt. % carbon monoxide present in an exhaust gas stream at temperatures of about 150° C. to about 200° C.
2 . The exhaust treatment device of claim 1 , wherein the protective layer is tin oxide.
3 . The exhaust treatment device of claim 1 , wherein protective layer has a thickness of less than or equal to 10 nm.
4 . The exhaust treatment device of claim 3 , wherein the thickness is about 1 nm to about 2 nm.
5 . The exhaust treatment device of claim 1 , wherein the platinum has a platinum particle size of less than or equal to 10 nanometers.
6 . The exhaust treatment device of claim 1 , wherein the catalyst further comprises tin, and wherein the platinum and tin each having a loading of about 0.1 wt. % to about 4.0 wt. %, based on the total weight of the catalyst.
7 . The exhaust treatment device of claim 1 , wherein the catalyst is capable of oxidizing greater than or equal to 80 wt. % carbon monoxide present in the exhaust gas stream at temperatures of about 250° C. to 350° C.
8 . The exhaust treatment device of claim 1 , wherein the catalyst is capable of oxidizing greater than or equal to 50 wt. % carbon monoxide present in the exhaust gas stream at temperatures of about 25° C. to 350° C.
9 . The exhaust treatment device of claim 1 , wherein the catalyst further comprises a solid solution support material, wherein the solid solution support material comprises lanthanum stabilized gamma-delta phase aluminum oxide, a titanium-zirconium solid solution, or a combination comprising at least one of the foregoing.
10 . The exhaust treatment device of claim 9 , wherein a molar ratio of gamma-delta aluminum oxide to titanium-zirconium solid solution is about 100:0 to about 60:40.
11 . The exhaust treatment device of claim 1 , further comprising a solid solution comprising solid solution comprising yttrium, zirconium, lanthanum, and titanium.
12 . A method of making an exhaust treatment device comprising:
disposing a support material on a substrate;
disposing platinum and an organometallic tin compound on the support material;
sintering the substrate at a temperature for a sufficient time and duration to decompose the organo portion of the organometallic tin compound, such that a protective layer comprising tin oxide forms over the platinum.
13 . The method of claim 12 , wherein the organometallic tin compound has the general formula:
[R] 3-4 X[A] 0-1
wherein X is tin, manganese, or iron; each R is independently a C 1 -C 40 alkyl, or a substituted C 1 -C 40 alkyl, and wherein the alkyl substituents comprise an alkoxy, an alkenyl, an alkynyl, a cycloalkyl, a cycloalkenyl, an acyl, a phenyl, a halosubstituted phenyl, a heteroaryl, or a combination comprising at least one of the foregoing substituents; and wherein A is a hydroxyl.
14 . The method of claim 12 , wherein the organometallic tin compound is selected from the group consisting of carboxylic acid type organometallic tin compounds; mercaptide type organometallic tin compounds; sulfide type organometallic tin compounds; organometallic tin oxides; and chloride type organometallic tin compounds.
15 . The method of claim 14 , wherein the organometallic tin compound is selected from the group consisting of (C 4 H 9 ) 2 Sn(OCOC 11 H 23 ) 2 , (C 4 H 9 ) 2 Sn(SCH 2 COOC 8 H 17 ) 2 , (C 4 H 9 ) 2 Sn═S, (C 4 H 9 ) 2 SnO, and (C 4 H 9 ) 2 SnCl 3 .
16 . A method of making a carbon monoxide oxidation catalyst, comprising:
forming a platinum protective layer bimetallic particle on a support material, wherein the protective layer material is selected from the group consisting of tin, iron, and manganese;
heating the supported bi-metallic particle to a sufficient temperature to form a catalyst comprising a protective layer on the platinum, wherein the protective layer is selected from the group consisting of tin oxide, iron oxide, manganese oxide; and wherein the catalyst is capable of oxidizing greater than or equal to 50 wt. % carbon monoxide present in an exhaust stream at temperature of about 150° C. to about 200° C.
17 . The method of claim 16 , wherein forming the platinum-protective bimetallic particle further comprises:
depositing the support material onto a substrate; and then co-depositing a platinum precursor and an organometallic protective layer precursor onto the support material.