NO2 abatement composition with enhanced sulfur resistance

Chemistry of inorganic compounds – Modifying or removing component of normally gaseous mixture – Mixture is exhaust from internal-combustion engine

Reexamination Certificate

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Details

C423S239100, C502S303000, C502S304000

Reexamination Certificate

active

06468484

ABSTRACT:

FIELD OF THE INVENTION
The present invention is broadly concerned with NO
x
abatement, particularly with NO
x
abatement in the exhaust gas of lean-burn internal combustion engines.
BACKGROUND OF THE INVENTION
It is well known in the art to utilize catalyst compositions, such as those commonly referred to as three-way conversion catalysts (“TWC”) to treat the exhaust gases of internal combustion engines. Such catalysts have been found to successfully promote both the oxidation of unburned hydrocarbons (“HC”) and carbon monoxide (“CO”), and the reduction of nitrogen oxides (“NO
x
”) in the exhaust gas, provided that the engine is operated at or close to an air/fuel ratio balanced for stoichiometric combustion (i.e., between about 14.4 and about 14.7; “combustion stoichiometry”). Currently, much research is underway to develop gasoline fueled engines, such as those used for passenger automobiles and the like, to operate under lean conditions, for at least part of the time, to achieve better fuel economy. Under lean conditions, the air to fuel ratio (A/F) and combustion mixture supplied to the engine are maintained above combustion stoichiometry so that the resulting exhaust gases are “lean”, i.e. the exhaust gases are relatively high in oxygen content and relatively low in reductant content, e.g. HC, CO and/or hydrogen.
Although lean burn engines provide enhanced fuel economy, they have the disadvantage that a conventional three-way conversion catalyst cannot adequately abate the NO
x
component of pollutants in the gas stream, as is required in order to meet increasingly stringent emission control regulations being implemented throughout the world. Efforts to increase NO
x
removal from exhaust gas emissions have resulted in the development of NO
x
adsorbers which typically comprise a sorbent material to remove NO
x
from a fuel-lean gas stream. While NO
x
adsorbers have been shown to remove NO
x
pollutants from exhaust gases, they suffer from the serious drawback that they are readily poisoned by sulfur also present in exhaust gases.
Without being bound to any particular theory of operation, it is believed that, under lean conditions, NO
x
present in the gas stream is sorbed onto the NO
x
adsorber in the form of stable metal nitrates, thereby removing NO
x
from the gas stream to be discharged to the atmosphere. A catalytic component is believed to promote such sorption. During rich conditions (i.e., high reductant content) reductants in the gas stream decompose the stable metal nitrates in the NO
x
adsorber, releasing NO
x
from the adsorber. The released NO
x
contacts a NO
x
abatement catalyst in the presence of reductants and, under suitable conditions (e.g., sufficiently elevated temperature), the NO
x
is reduced to nitrogen or to nitrogen and N
2
O.
By a mechanism similar to that for the formation of the stable metal nitrates, sulfur oxides present in the gas stream are sorbed onto the NO
x
adsorber in the form of very stable metal sulfate salts. Unlike the storage nitrates which readily decompose under rich conditions, decomposition of the metal sulfates requires a combination of rich gas and elevated operating temperature. This combination of conditions may not occur with sufficient frequency under normal operating conditions for typical lean bum gasoline and diesel engines. As a result, the NO
x
storage sites are gradually poisoned by sulfur, and the NO
x
conversion capability of the catalyst gradually degrades to unacceptable levels for efficient exhaust purification.
The NO
x
adsorber compositions disclosed herein provide enhanced recovery from poisoning by sulfur compounds, while retaining their NO
x
abatement efficiency.


REFERENCES:
patent: 5863508 (1999-01-01), Lachman et al.
patent: 5874057 (1999-02-01), Deeba et al.
patent: 5888464 (1999-03-01), Wu et al.
patent: 5916129 (1999-06-01), Modica et al.
patent: 5939037 (1999-08-01), Hepburn et al.
patent: 931590 (1999-07-01), None

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