US2005197244A1PendingUtilityA1
Exhaust treatment system and catalyst system
Priority: Mar 5, 2004Filed: Mar 5, 2004Published: Sep 8, 2005
Est. expiryMar 5, 2024(expired)· nominal 20-yr term from priority
Inventors:Moroz L'VovichKarl KharasMikhail Yurievich SmirnovBobrin AlexanderValerii Ivanovich Bukhtlyarov
B01D 2257/502B01D 53/945B01J 23/40B01D 53/944B01D 2257/702Y02T10/12B01J 37/0246B01J 23/56B01J 29/7415B01D 2255/106B01J 23/52B01D 2255/912B01J 35/19
33
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Claims
Abstract
A catalyst system comprises a gold catalyst capable of oxidizing CO; a hydrocarbon oxidation catalyst; and a hydrocarbon adsorbing material.
Claims
exact text as granted — not AI-modified1 . A catalyst system comprising:
a gold catalyst capable of oxidizing CO; a hydrocarbon oxidation catalyst; and a hydrocarbon adsorbing material.
2 . The catalyst system of claim 1 , wherein the gold catalyst, the hydrocarbon oxidation catalyst, and the hydrocarbon adsorbing material are in a physical mixture.
3 . The catalyst system of claim 1 , wherein the hydrocarbon oxidation catalyst; and the hydrocarbon adsorbing material are disposed upstream of the gold catalyst.
4 . The catalyst system of claim 1 , wherein a first substrate comprises the gold catalyst, the hydrocarbon oxidation catalyst, and the hydrocarbon adsorbing material disposed thereon; and a second substrate located upstream of the first substrate comprises the hydrocarbon oxidation catalyst, and the hydrocarbon adsorbing material disposed thereon.
5 . The catalyst system of claim 1 , further comprising a support material disposed on a substrate, wherein the gold catalyst and the hydrocarbon catalyst are disposed on the support material.
6 . The catalyst system of claim 5 , wherein the support material is an alumina selected from the group consisting of the gamma alumina, delta alumina, and theta alumina.
7 . The catalyst system of claim 1 , wherein the gold catalyst has a gold particle size less than or equal to about 10 nm.
8 . The catalyst system of claim 7 , wherein the gold particle size is less than or equal to about 7 nm.
9 . The catalyst system of claim 8 , wherein the gold particle size is less than or equal to about 4 nm.
10 . The catalyst system of claim 1 , wherein the hydrocarbon oxidation catalyst is platinum or palladium, and the adsorption material is selected from the group consisting of beta zeolite, ultra-stable Y zeolite and UTD-1 zeolite.
11 . The catalyst system of claim 1 , wherein a ratio of a gold catalyst volume to a hydrocarbon oxidation volume is greater than or equal to about 1:12.5.
12 . The catalyst system of claim 1 , wherein the gold catalyst is capable of converting greater than or equal to 50% CO present in an exhaust stream to CO 2 at temperatures less than or equal to about 100° C. in an atmosphere comprising a hydrocarbon at a space velocity less than or equal to 250,000 hr −1 .
13 . The catalyst system of claim 12 , wherein the space velocity is less than or equal to about 37,000 hr −1 .
14 . The catalyst system of claim 13 , wherein the space velocity is less than or equal to about 25,000 hr −1 .
15 . The catalyst system of claim 1 , wherein the catalyst system is used in an exhaust treatment system.
16 . The catalyst system of claim 1 , wherein the catalyst system is used in air purification system for a household use.
17 . A method of using a catalyst system comprising:
passing an exhaust stream over a catalyst system comprising a gold catalyst capable of oxidizing CO, a hydrocarbon oxidation catalyst; and a hydrocarbon adsorbing material; and oxidizing at least a portion of CO present in the exhaust stream.
18 . The method of claim 17 , wherein the gold catalyst, the hydrocarbon oxidation catalyst, and the hydrocarbon adsorbing material are in a physical mixture.
19 . The method of claim 17 , wherein the hydrocarbon oxidation catalyst; and the hydrocarbon adsorbing material are disposed upstream of the gold catalyst.
20 . The method of claim 17 , wherein a first substrate comprises the gold catalyst, the hydrocarbon oxidation catalyst, and the hydrocarbon adsorbing material disposed thereon; and a second substrate located upstream of the first substrate comprises the hydrocarbon oxidation catalyst, and the hydrocarbon adsorbing material disposed thereon.
21 . The method of claim 17 , wherein greater than or equal to 50% CO in the exhaust stream is converted to CO 2 at a space velocity less than or equal to 250,000 hr −1 at a temperature less than or equal to about 100° C.
22 . The catalyst system of claim 21 , wherein the space velocity is less than or equal to about 37,000 hr −1 .
23 . The catalyst system of claim 22 , wherein the space velocity is less than or equal to about 25,000 hr −1 .Join the waitlist — get patent alerts
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