Catalyst for oxidizing carbon monoxide and method of manufacturing the same
Abstract
A catalyst that oxidizes carbon monoxide includes a bimetal consisting of platinum and a transition metal in a bimetallic phase that is loaded on γ-alumina support. The catalyst is manufactured by uniformly mixing a platinum precursor, a transition metal precursor, and γ-alumina (γ-Al 2 O 3 ) in a dispersion medium to provide a mixture; drying the mixture; calcining the dried mixture; and reducing the calcined dried mixture. Since the catalyst that oxidizes carbon monoxide has high reaction activity even at low temperature and excellent reaction selectivity, and a methanation reaction and reoxidization do not occur, and the catalyst can effectively eliminate carbon monoxide in the fuel.
Claims
exact text as granted — not AI-modified1 . A catalyst that oxidizes carbon monoxide, comprising a bimetal consisting of platinum (Pt) and a transition metal other than platinum in a bimetallic phase, wherein the bimetal is loaded on a γ-alumina (γ-Al 2 O 3 ) support, and wherein the transition metal of the bimetal is reduced.
2 . The catalyst of claim 1 , wherein the catalyst has a peak between 130 to 180° C. in a temperature programmed reduction (TPR) analysis and is not reoxidized until the temperature reaches 500° C. in a temperature programmed oxidation (TPO) analysis.
3 . The catalyst of claim 1 , wherein the transition metal is selected from the group consisting of Ni, Co, Cu, and Fe.
4 . The catalyst of claim 1 , wherein the atomic ratio of the transition metal to platinum is from 0.5 to 20.
5 . The catalyst of claim 1 , wherein the amount of platinum is in the range of 0.3 to 5% by weight based on the weight of the catalyst.
6 . The catalyst of claim 1 , wherein the catalyst has a reaction selectivity such that when the catalyst oxidizes carbon monoxide, a methanation reaction does not occur.
7 . A method of manufacturing a catalyst that oxidizes carbon monoxide, the method comprising:
uniformly mixing a platinum precursor, a transition metal precursor, and γ-alumina (γ-Al 2 O 3 ) in a dispersion medium to provide a mixture; drying the mixture; calcining the dried mixture; and reducing the calcined dried mixture.
8 . The method of claim 7 , wherein the weight ratio of the platinum precursor and the transition metal precursor is adjusted such that the atomic ratio of the transition metal to platinum is from 0.5 to 20.0.
9 . The method of claim 7 , wherein the calcining is performed at a temperature of 300 to 500° C. for 1 to 12 hours.
10 . The method of claim 7 , wherein the reducing is performed at a temperature of 150 to 500° C. for 1 to 12 hours.
11 . The method of claim 7 wherein the platinum precursor and the transition metal precursor are compounds that do not contain a halogen.
12 . The method of claim 7 , wherein the platinum precursor is Pt(NH 3 ) 4 (NO 3 ) 2 .
13 . The method of claim 7 , wherein the transition metal precursor is selected from the group consisting of Ni(NO 3 ) 2 .6H 2 O, Co(NO 3 ) 2 .6H 2 O, Cu(NO 3 ) 2 .H 2 O and Fe(NO 3 ) 2 .9H 2 O.
14 . A fuel processor comprising the catalyst of claim 1 .
15 . A fuel processor of claim 14 , comprising a desulfurization device, at least one shift reaction device, and a PROX reaction device, wherein the catalyst is included in the PROX reaction device.
16 . A fuel cell system comprising the catalyst of claim 1 .
17 . A fuel cell system of claim 16 , comprising a fuel cell stack and a fuel processor, wherein the catalyst is included in the fuel processor.
18 . A fuel cell system of claim 17 , wherein the fuel processor comprises a desulfurization device, at least one shift reaction device, and a PROX reaction device, and wherein the catalyst is included in the PROX reaction device.Join the waitlist — get patent alerts
Track US2007092768A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.