Method and system for maintaining efficiency of a three-way...

Power plants – Internal combustion engine with treatment or handling of... – By means producing a chemical reaction of a component of the...

Reexamination Certificate

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C060S274000, C060S284000, C060S289000

Reexamination Certificate

active

06634169

ABSTRACT:

This invention concerns improvements relating to catalysts more especially it concerns improvements in automobile emission catalysts.
The use of such catalysts, also known as catalytic converters, is very well established in the automobile industry in view of the exhaust gas emission regulations which are in force in most countries. The most common catalysts use a platinum group metal (“PGM”) especially one or more of Pt, Pd and Rh, carried on an oxidic high surface area washcoat which is one or more of Al
2
O
3
, CeO
2
, ZrO
2
including mixed oxides thereof or the like. The support for the catalyst is generally a low pressure-drop flow-through honeycomb manufactured from an extruded ceramic, eg cordierite, or from a metal honeycomb.
Gasoline contains varying amounts of sulphur depending upon its origins and the amount and type of refining it has been subjected to. Sulphur is a well-known poison of catalyst activity in such catalysts. We believe that the deactivating effect of sulphur may be due to adsorption on either the precious metal or on the support. We have found that sulphur may be removed by increasing the temperature of the catalyst, but that under lean operating conditions, that is when the overall composition of the exhaust gases leaving the engine is oxidising, the temperature required for sulphur removal is higher than under rich conditions. Indeed, we have found that for certain catalysts, the minimum temperature for sulphur removal is 625° C. under lean conditions. This temperature is higher than the catalyst would normally be exposed to in its usual under-floor position mounted on the automobile.
EP 580389 (Toyota) discloses the removal of SOx from a NOx absorbent-type catalyst which is used to treat the exhaust gases from a lean-burn gasoline internal combustion engine, by decreasing the oxygen concentration in the exhaust gases, thus making them rich. That is, SOx is being removed from the NOx absorbent by chemical means. JP 4161251 (Mitsubishi) teaches the removal of SOx from a catalyst for a lean burn internal combustion engine such as a diesel engine, by heating the catalyst to 450-800° C. It is plain from the drawings that significant heating is required (600° C. for 1 hour) in order approximately the S-free conversion. Heating at 500° C. for 2 hours did not give to return to approximately the S-free conversion. Heating at 500° for 2 hours did not give such good results. Most diesel fuels have a much higher S content than gasolines.
According to one aspect, the invention provides a system comprising a gasoline-fuelled internal combustion engine, which engine operates substantially under stoichiometric conditions during normal operation, a three-way catalyst (TWC) mounted under-floor and arranged in an exhaust passage to have exhaust gas passed continuously therethrough, and an engine management system, wherein the engine management system is programmed to initiate a condition of the system in which the engine exhaust gases are enriched with at least one of CO and hydrocarbons; and secondary air is added to the engine exhaust gases in the exhaust passage upstream of the underfloor TWC to make the exhaust gas leaner over the underfloor TWC than the exhaust gas exiting the engine and to cause an exotherm by oxidation of the at least one of CO and hydrocarbons over the underfloor TWC thereby to raise the underfloor TWC temperature to at least 550° C., whereby sulphur poisoning of the catalyst is reduced, during at least one portion of every operation of the engine.
According to a further aspect, the invention provides a method of reducing sulphur poisoning of a three-way catalyst (TWC) in the exhaust system of a gasoline-fuelled internal combustion engine, which method comprises operating the engine at substantially stoichiometric conditions during normal operation; intermittently enriching the exhaust gases exiting the engine with at least one of CO and hydrocarbons; and adding supplementary air to the exhaust gases upstream of the TWC to make them leaner than the exhaust gas exiting the engine thereby to cause catalytic oxidation of the at least one of CO and hydrocarbons to cause heating of the TWC, thereby to raise the temperature of the TWC to at least 550° C., preferably at least 600° C., whilst continuously passing exhaust gas therethrough, provided that said intermittent enrichment and air addition takes place at least once every engine operation.
The internal combustion engine and its associated controls may be desirably designed in a preferred embodiment to operate essentially under stoichiometric conditions during normal operation.
A preferred catalyst for use in this preferred embodiment incorporates palladium and ceria. A more preferred catalyst is one having ambient temperature CO oxidation activity, as described in our prior patent applications WO 96/39576 and EP 0747581.
The preferred embodiment of the present invention may be operated in several different ways. In a first method, especially when using the preferred catalysts, the engine management system provides a very rich cold start. Oxidation of CO and unburnt hydrocarbon species (using a secondary air supply) on the catalyst immediately begins to raise the catalyst temperature to a temperature at which sulphur removal under lean conditions takes place, that is preferably above 625° C. More preferably, the rich cold start is continued to bring the catalyst to a temperature of 800-850° C. or higher, in order to remove virtually all sulphur species from the catalyst.
A second method, which may be combined with the first, utilises a periodic enrichment to, for example, an air/fuel ratio of 10-14 for a pre-set time, for example 5-100 seconds, during normal running, combined with secondary air addition. The catalyst will already be at a normal operating temperature of at least 400° C. and therefore does not require as much chemical energy to raise its temperature to an effective sulphur-removal temperature as does the first embodiment which begins at ambient temperature. In such a second method, the period between initiations of the high temperature may be pre-set in the engine management system memory, or may be variable according to operating conditions and/or either the sulphur content of the fuel, eg as sensed, or some form of feed-back of sulphidation of the catalyst.
A modification of this second method arises in a preferred design in which the said catalyst is supplemented by another catalyst, preferably in a close-coupled position close to the engine. The close-coupled catalyst is mounted upstream of the secondary air inlet. This offers particular benefits in that during the high temperature phase, NOx reduction on the main catalyst is less effective (because of the lean condition due to secondary air addition), but the close-coupled catalyst, which is exposed to the enriched engine-out condition, can still provide NOx removal.
A third method involves removal of sulphur under rich conditions, which may be achieved at a lower catalyst temperature than when the exhaust gas is stoichiometric or lean. The normal operating temperature of the catalyst is still generally below that at which sulphur may be removed. It is therefore again necessary to raise the catalyst temperature which may be done by enrichment, either on start-up or periodically during operation, by adjusting the air-fuel ratio fed to the engine or by supplementary fuel addition into the exhaust gas stream. Supplementary air addition provides the conditions for exothermic oxidation on the catalyst raising its temperature to or above the required level. Once the required temperature has been reached, suitably at least 550° C., preferably at least 650° C., the supplementary air may be terminated or reduced, so that the exhaust gases are rich, that is there is an excess of reducing species.
It will be appreciated that the actual conditions, time periods and other parameters relevant to sulphur removal depend upon the engine and emission system design and general operating conditions, as well as the results desired, and may be

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