Method for purifying combustion exhaust gas

BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to a process for purifying combustion exhaust gas and a device used in the process. More specifically, the present invention relates to a process which is capable of effectively resolving HC, CO and NO.sub.x components, as well as an NH.sub.3 component, in the combustion exhaust gas such as the exhaust gas from internal combustion engines, boilers and furnaces, and a device suitable for performing that process (in this specification, the term NO.sub.x means any nitrogen oxide such as NO, NO.sub.2, N.sub.2 O and N.sub.3 O.sub.4, further, the term "resolving" means removing components in the exhaust gas, for example, by converting the components to other components by chemical reactions).
2. Description of the Related Art
A process for resolving three pollutants in a combustion exhaust gas, i.e., a hydrocarbon component (HC), a carbon-monoxide component (CO), and nitrogen-oxide components (NO.sub.x), simultaneously is disclosed in, for example, Japanese Unexamined Patent Publication No. 53-86917. In the process disclosed in the '917 publication, the exhaust gas from an internal combustion engine is fed to a three-way reducing and oxidizing catalyst at an air-fuel ratio lower than the stoichiometric air-fuel ratio (i.e., a rich air-fuel ratio) and, after it passes through the three-way reducing and oxidizing catalyst, secondary air is added to the exhaust gas so that the air-fuel ratio of the exhaust gas becomes higher than the stoichiometric air-fuel ratio (i.e., a lean air-fuel ratio). Then, the exhaust gas of the lean air-fuel ratio is fed to an oxidizing catalyst. Namely, in the process disclosed in '917 publication, the combustion exhaust gas from the engine is first fed to a three-way reducing and oxidizing catalyst in a reducing atmosphere, and after it passes through the three-way reducing and oxidizing catalyst, the atmosphere of the exhaust gas is changed to an oxidizing atmosphere. Then, this exhaust gas with an oxidizing atmosphere is fed to an oxidizing catalyst.
As is well known in the art, a three-way reducing and oxidizing catalyst is capable of simultaneously oxidizing HC and CO components and reducing NO.sub.x components in the exhaust gas when the air-fuel ratio of the exhaust gas is in a narrow air-fuel ratio range around the stoichiometric air-fuel ratio. However, when the air-fuel ratio of the exhaust gas is on the lean air-fuel ratio side compared to the above air-fuel ratio range (i.e., in an oxidizing atmosphere), the ability of the three-way reducing and oxidizing catalyst for reducing NO.sub.x components falls rapidly. Further, when the air-fuel ratio of the exhaust gas is on a rich side compared to the above optimum range (i.e., in a reducing atmosphere), the ability of the three-way reducing and oxidizing catalyst for oxidizing HC and CO components falls rapidly. Therefore, when a three-way reducing and oxidizing catalyst is used for resolving HC, CO and NO.sub.x components at the same time, it is necessary to control the engine so that the engine is always operated at an air-fuel ratio in the narrow air-fuel ratio range around the stoichiometric air-fuel ratio. In the actual operation of the engine, it is very difficult to maintain the operating air-fuel ratio of the engine strictly in such a narrow range in all operating conditions, and in some cases, emission of these components increases when the air-fuel ratio of the exhaust gas deviates from the optimum air-fuel ratio range.
In order to solve this problem, the internal combustion engine is operated at an air-fuel ratio lower than the stoichiometric air-fuel ratio in the process disclosed in the '917 publication and the air-fuel ratio of the exhaust gas is maintained on a rich side compared to the stoichiometric air-fuel ratio regardless of the change in the operating conditions of the engine. This rich air-fuel ratio exhaust gas is fed to the three-way reducing and oxidizing catalyst. Since the ability of the three-way reducing and oxidizing catalyst for reducing NO.sub.x components is high when the air-fuel ratio of the exhaust gas is rich, almost all of the NO.sub.x components in the exhaust gas are reduced by the reducing and oxidizing catalyst. Further, a portion of HC, CO components in the exhaust gas are oxidized by the reducing and oxidizing catalyst. After it passes through the three-way reducing and oxidizing catalyst, secondary air is supplied to the exhaust gas to adjust the air-fuel ratio of the exhaust gas so that the air-fuel ratio of the exhaust gas becomes lean, and this lean air-fuel ratio exhaust gas is, then fed to the oxidizing catalyst. Therefore, the portions of HC, CO components in the exhaust gas which are not oxidized by the three-way reducing and oxidizing catalyst are oxidized by the oxidizing catalyst in an oxidizing atmosphere.
According to the process in the '917 publication, NO.sub.x components and part of the HC, CO components are resolved by contacting the exhaust gas from the engine with the three-way reducing and oxidizing catalyst in a reducing atmosphere, and the remaining portion of the HC, CO components are resolved by contacting the exhaust gas in an oxidizing atmosphere with the oxidizing catalyst after it has passed through the three-way reducing and oxidizing catalyst, Since the air-fuel ratio of the exhaust gas from the engine is adjusted so that the air-fuel ratio becomes rich (a reducing atmosphere), then lean (an oxidizing atmosphere) in the process in the '917 publication, i.e., it is not required to maintain the air-fuel ratio of the exhaust gas in the narrow optimum range, HC, CO and NO.sub.x components in the exhaust gas can be resolved at high efficiency regardless of the operating condition of the engine.
However, one problem arises when the process in the '917 publication is used for resolving HC, CO and NO.sub.x components. The three-way reducing and oxidizing catalyst, though it has a high ability for reducing NO.sub.x components in a reducing atmosphere, also converts a portion of NO.sub.x components in the exhaust gas to NH.sub.3 component (ammonia) in a reducing atmosphere. In the process in the '917 publication, since the rich air-fuel ratio exhaust gas is fed to the three-way reducing and oxidizing catalyst, the exhaust gas which flows out from the three-way reducing and oxidizing catalyst contains a small amount of NH.sub.3. This NH.sub.3 in the exhaust gas is oxidized and again produces NO.sub.x when the exhaust gas is fed to the oxidizing catalyst in an oxidizing atmosphere. Therefore, when the process in the '917 publication is used, it is difficult to resolve NO.sub.x components in the exhaust gas completely, since NO.sub.x components are produced by the oxidizing catalyst.
SUMMARY OF THE INVENTION
In view of the problems in the related art, the object of the present invention is to provide a process and a device for purifying a combustion exhaust gas which is capable of resolving substantially all of the HC, CO, and NO.sub.x components as well as a NH.sub.3 component in the exhaust gas while preventing NO.sub.x from being produced by the oxidation of NH.sub.3 contained in the exhaust gas.
The above object is achieved by a process for resolving NH.sub.3 in a combustion exhaust gas by contacting a combustion exhaust gas containing NH.sub.3 in an oxidizing atmosphere at a temperature within a predetermined range to an NH.sub.3 decomposing catalyst which resolves NH.sub.3 in an exhaust gas in an oxidizing atmosphere when the temperature of the catalyst is in the predetermined temperature range, converts NH.sub.3 in the exhaust gas in an oxidizing atmosphere to NO.sub.x components when the temperature of the catalyst is higher than the predetermined temperature range, and allows NH.sub.3 in the exhaust gas in an oxidizing atmosphere to pass through the catalyst when the temperature of the catalyst is lower than the predetermined temperature range.
The NH.sub.3 decomposing catalyst is capable of resolving NH.sub.3 in the exhaust gas in an oxidizing atmosphere when the temperature of the catalyst is within the predetermined temperature range. Therefore, by feeding the exhaust gas containing NH.sub.3 to the NH.sub.3 decomposing catalyst in an oxidizing atmosphere and at a temperature within the predetermined range, substantially all of NH.sub.3 in the exhaust gas is resolved by the NH.sub.3 decomposing catalyst without forming NO.sub.x components.
According to another aspect of the present invention, there is provided a process for resolving pollutants in the exhaust gas of an internal combustion engine comprising, contacting an exhaust gas of an internal combustion engine in a reducing atmosphere with an NH.sub.3 synthesizing catalyst which converts NO.sub.x components in the exhaust gas, in a reducing atmosphere, to NH.sub.3, adjusting the conditions of the exhaust gas after it contacts the NH.sub.3 synthesizing catalyst so that the exhaust gas is in an oxidizing atmosphere and within a predetermined temperature range, and contacting the exhaust gas, after its atmosphere and temperature are adjusted, with an NH.sub.3 decomposing catalyst which resolves NH.sub.3 in the exhaust gas in an oxidizing atmosphere when the temperature of the catalyst is in a predetermined temperature range, converts NH.sub.3 in the exhaust gas in an oxidizing atmosphere to NO.sub.x components when the temperature of the catalyst is higher than the predetermined temperature range, and allows NH.sub.3 in the exhaust gas in an oxidizing atmosphere to pass through the catalyst when the temperature of the catalyst is lower than the predetermined temperature range.
In this aspect of the invention, the exhaust gas from the internal combustion engine contacts the NH.sub.3 synthesizing catalyst in an reducing atmosphere. Therefore, the NO.sub.x component in the exhaust gas is converted to NH.sub.3. Further, after it contacts the NH.sub.3 synthesizing catalyst, the exhaust gas contacts the NH.sub.3 decomposing catalyst in an oxidizing atmosphere and at the temperature within the predetermined temperature range. Thus, substantially all of NH.sub.3 produced by the NH.sub.3 synthesizing catalyst is resolved by the NH.sub.3 decomposing catalyst, and the exhaust gas flowing out from the NH.sub.3 decomposing catalyst is completely free from the NO.sub.x and NH.sub.3.
Further, the NH.sub.3 synthesizing catalyst in the present invention is capable of resolving most of pollutants in the exhaust gas when the exhaust gas is in a reducing atmosphere (i.e., when the oxygen concentration in the exhaust gas is low). For example, the pollutants such as HC, CO and NO in the exhaust gas are resolved by the NH.sub.3 synthesizing catalyst by the following reactions when the exhaust gas is in a reducing atmosphere.
(CH.sub.2).sub.m +(3m/2)O.sub.2 .fwdarw.mCO.sub.2 +mH.sub.2 O (1)
CO+(1/2)O.sub.2 .fwdarw.CO.sub.2 ( 2)
NO+CO.fwdarw.(1/2)N.sub.2 +CO.sub.2 ( 3)
However, since the oxygen concentration is low when the exhaust gas is in a reducing atmosphere, a portion of CO and HC in the exhaust gas is not resolved by the above reactions (1) and (2), and a small amount of CO and HC are resolved by the following reactions.
(CH.sub.2).sub.n +(n/2)O.sub.2 .fwdarw.nCO+nH.sub.2 ( 4)
(CH.sub.2).sub.n +nH.sub.2 O.fwdarw.nCO+2nH.sub.2 ( 5)
CO+H.sub.2 O.fwdarw.CO.sub.2 +H.sub.2 ( 6)
When H.sub.2 is formed by the reactions (4) through (6), NO in the exhaust gas reacts H.sub.2 and a small amount of NH.sub.3 is formed by the following reaction.
NO+(5/2)H.sub.2 .fwdarw.NH.sub.3 +H.sub.2 O
The speed of the reactions (4) through (6) are slow compared with the reactions (1) through (3), and when the oxygen concentration of the exhaust gas is low (for example, the excess air ratio .lambda. of the exhaust gas is lower than 0.95), the reactions (4) through (6) are not likely to occur, and in this case CO and HC pass through the NH.sub.3 synthesizing catalyst without being resolved. Therefore, to produce NH.sub.3 by the NH.sub.3 synthesizing catalyst, the excess air ratio .lambda. of the exhaust gas must be slightly lower than 1.0, for example, the value of .lambda. must be .lambda.=0.95 to 1.0 and preferably between 0.98 and 1.0.
According to another aspect of the present invention, there is provided a device for resolving NH.sub.3 contained in the exhaust gas of an internal combustion engine comprising an NH.sub.3 decomposing catalyst disposed on an exhaust gas passage of an internal combustion engine, wherein the NH.sub.3 decomposing catalyst resolves NH.sub.3 in an exhaust gas flowing into the catalyst in an oxidizing atmosphere when the temperature of the catalyst is in a predetermined temperature range, converts NH.sub.3 in the exhaust gas flowing into the catalyst in an oxidizing atmosphere to NO.sub.x components when the temperature of the catalyst is higher than the predetermined temperature range, and allows NH.sub.3 in an exhaust gas in an oxidizing atmosphere to pass through the catalyst when the temperature of the catalyst is lower than the predetermined temperature range, oxygen supply means for supplying oxygen to the exhaust gas flowing into the NH.sub.3 decomposing catalyst so that the exhaust gas flowing into the NH.sub.3 decomposing catalyst becomes an oxidizing atmosphere, and a temperature maintaining means for maintaining the temperature of the exhaust gas flowing into the NH.sub.3 decomposing catalyst within the predetermined temperature range regardless of change in the temperature of the exhaust gas discharged from the internal combustion engine.
In this aspect of the invention, the oxygen supply means adjust the conditions of the exhaust gas so that the exhaust gas becomes an oxidizing atmosphere, and the temperature maintaining means maintains the temperature of the exhaust gas within the predetermined temperature range. Thus, an exhaust gas is fed to the NH.sub.3 decomposing catalyst in an oxidizing atmosphere and at the temperature within the predetermined temperature, and NH.sub.3 in the exhaust gas is resolved by the NH.sub.3 decomposing catalyst.
According to another aspect of the invention, there is provided a device for resolving NH.sub.3 contained in the exhaust gas of an internal combustion engine comprising a plurality of NH.sub.3 decomposing catalysts disposed on the exhaust gas passage in series arrangement wherein each of the NH.sub.3 decomposing catalysts resolves NH.sub.3 in the exhaust gas flowing into the catalyst in an oxidizing atmosphere when the temperature of the catalyst is in a predetermined temperature range, converts NH.sub.3 in the exhaust gas flowing into the catalyst in an oxidizing atmosphere to NO.sub.x components when the temperature of the catalyst is higher than the predetermined temperature range, and allows NH.sub.3 in an exhaust gas in an oxidizing atmosphere to pass through the catalyst when the temperature of the catalyst is lower than the predetermined temperature range, oxygen supply means for supplying oxygen selectively to the exhaust gas flowing into the respective NH.sub.3 decomposing catalysts, temperature detecting means for detecting the temperature of the respective NH.sub.3 decomposing catalysts, and selecting means for controlling the oxygen supply means in such a manner that the oxygen supply means supplies oxygen to the exhaust gas flowing into the NH.sub.3 decomposing catalyst(s) whose temperature is within the predetermined temperature range.
In this aspect of the invention, more than one NH.sub.3 decomposing catalyst is disposed on the exhaust gas passage of the engine in a series arrangement. Since the temperature of the exhaust gas from the engine becomes low as the exhaust gas flows down the exhaust gas passage due to the heat dissipation through the wall of the exhaust gas passage, the temperatures of the exhaust gas flowing into the respective NH.sub.3 decomposing catalyst are different from each other according to the location of the catalyst. Consequently, the temperatures of the NH.sub.3 decomposing catalysts are also different from each other. The selecting means selects the NH.sub.3 decomposing catalyst, which has a temperature within the predetermined range, and controls the oxygen supply means so that oxygen is supplied to the NH.sub.3 decomposing catalyst having a temperature within the predetermined range. Therefore, the exhaust gas in an oxidizing atmosphere is supplied to the NH.sub.3 decomposing catalyst at a temperature within the predetermined temperature range, and NH.sub.3 in the exhaust gas is effectively resolved by the NH.sub.3 decomposing catalyst even if the temperature of the exhaust gas at the outlet of the engine changes due to a change in the operating condition of the engine.
According to another aspect of the present invention, there is provided a process for resolving NO.sub.x in a combustion exhaust gas using an NH.sub.3 decomposing catalyst which resolves NO.sub.x in the exhaust gas in an oxidizing atmosphere under the presence of an NH.sub.3 when the temperature of the catalyst is within a predetermined temperature range, converts the NH.sub.3 in the exhaust gas in an oxidizing atmosphere when the temperature of the catalyst is higher than the predetermined temperature range, and allows the NH.sub.3 in the exhaust gas in an oxidizing atmosphere to pass through the catalyst when the temperature of the catalyst is lower than the predetermined temperature range comprising, supplying NH.sub.3 to an exhaust gas from an internal combustion engine, and contacting the exhaust gas to the NH.sub.3 decomposing catalyst in an oxidizing atmosphere and at the temperature within the predetermined temperature range.
In this aspect of the invention, the NH.sub.3 decomposing catalyst resolves the NO.sub.x by reacting a NH.sub.3 with NO.sub.x components in the exhaust gas in an oxidizing atmosphere when the temperature is within a predetermined temperature range. Since NH.sub.3 is added to the exhaust gas before the exhaust gas is fed to the NH.sub.3 decomposing catalyst in this aspect of the invention, the exhaust gas flowing into the NH.sub.3 decomposing catalyst in oxidizing atmosphere and at the temperature within the predetermined temperature range contains NO.sub.x and NH.sub.3, the NO.sub.x in the exhaust gas react with the NH.sub.3 on the NH.sub.3 decomposing catalyst and are resolved.
According to another aspect of the present invention, there is provided a device for resolving NO.sub.x in the exhaust gas of an internal combustion engine operated at an air-fuel ratio higher than the stoichiometric air-fuel ratio comprising an NH.sub.3 decomposing catalyst disposed on an exhaust gas passage of an internal combustion engine, wherein the NH.sub.3 decomposing catalyst resolves NO.sub.x in the exhaust gas flowing into the catalyst in an oxidizing atmosphere under the presence of an NH.sub.3 when the temperature of the catalyst is in a predetermined temperature range, converts the NH.sub.3 in the exhaust gas flowing into the catalyst in an oxidizing atmosphere to NO.sub.x when the temperature of the catalyst is higher than the predetermined temperature range, and allows the NH.sub.3 in the exhaust gas in an oxidizing atmosphere to pass through the catalyst when the temperature of the catalyst is lower than the predetermined temperature range, an NH.sub.3 supply means for supplying NH.sub.3 to the exhaust gas flowing into the NH.sub.3 decomposing catalyst, and temperature maintaining means for maintaining the temperature of the exhaust gas flowing into the NH.sub.3 decomposing catalyst within the predetermined temperature range regardless of change in the temperature of the exhaust gas discharged from the internal combustion engine.
In this aspect of the invention, the internal combustion engine is operated at a lean air-fuel ratio and the exhaust gas from the engine is in an oxidizing atmosphere. NH.sub.3 is added to this exhaust gas before the exhaust gas flows into the NH.sub.3 decomposing catalyst. Further, the temperature of the exhaust gas is maintained within the predetermined range. Therefore, the exhaust gas containing NO.sub.x and a NH.sub.3 is fed to the NH.sub.3 decomposing catalyst in an oxidizing atmosphere and at the temperature within the predetermined temperature range, and the NO.sub.x in the exhaust gas reacts the NH.sub.3 component at the NH.sub.3 decomposing catalyst and resolved.
According to another aspect of the present invention, there is provided a device for resolving NO.sub.x in an exhaust gas of an internal combustion engine operated at an air-fuel ratio higher than the stoichiometric air-fuel ratio comprising a plurality of NH.sub.3 decomposing catalysts disposed on the exhaust gas passage in series arrangement wherein each of the NH.sub.3 decomposing catalysts resolves NO.sub.x in the exhaust gas flowing into the catalyst in an oxidizing atmosphere under the presence of an NH.sub.3 when the temperature of the catalyst is in a predetermined temperature range, converts the NH.sub.3 in the exhaust gas flowing into the catalyst in an oxidizing atmosphere to NO.sub.x when the temperature of the catalyst is higher than the predetermined temperature range, and allows the NH.sub.3 in the exhaust gas in an oxidizing atmosphere to pass through the catalyst when the temperature of the catalyst is lower than the predetermined temperature range, an NH.sub.3 supply means for supplying NH.sub.3 selectively to the exhaust gas flowing into the respective NH.sub.3 decomposing catalysts, temperature detecting means for detecting the temperature of the respective NH.sub.3 decomposing catalysts, and selecting means for controlling the NH.sub.3 supply means in such a manner that the NH.sub.3 supply means supplies NH.sub.3 to the exhaust gas flowing into the NH.sub.3 decomposing catalysts whose temperature is within the predetermined temperature range.
In this aspect of the invention, more than one NH.sub.3 decomposing catalysts are disposed on the exhaust gas passage of the engine. Since the temperature of the exhaust gas becomes lower as the exhaust gas flows down the exhaust gas passage, the temperatures of the respective NH.sub.3 decomposing catalysts vary in accordance with the location of the NH.sub.3 decomposing catalysts. Therefore, even when the temperature of the exhaust gas changes due to change in the operating condition of the engine, some of the NH.sub.3 decomposing catalysts always stay in the predetermined temperature range. A selecting means controls the NH.sub.3 supply means so that NH.sub.3 is supplied to the exhaust gas flowing into the NH.sub.3 decomposing catalysts which has a temperature within the predetermined range. Therefore, exhaust gas in an oxidizing atmosphere containing NH.sub.3 and NO.sub.x is fed to the NH.sub.3 decomposing catalyst which has the temperature within the predetermined range. Consequently, the NO.sub.x in the exhaust gas reacts the NH.sub.3 at the NH.sub.3 decomposing catalyst and resolved.
According to another aspect of the present invention, there is provided a device for resolving NO.sub.x components in an exhaust gas of an internal combustion engine, the operating air-fuel ratio of the engine fluctuates around the stoichiometric air-fuel ratio in such a manner that the average operating air-fuel ratio of the engine is higher than the stoichiometric air-fuel ratio, the device comprises an NH.sub.3 synthesizing catalyst disposed on an exhaust gas passage of the engine, wherein the NH.sub.3 synthesizing catalyst converts NO.sub.x in the exhaust gas discharged from the engine when the operating air-fuel ratio of the engine is lower than the stoichiometric air-fuel ratio to NH.sub.3 and N.sub.2, and an NH.sub.3 decomposing catalyst disposed on the exhaust gas passage downstream of the NH.sub.3 synthesizing catalyst, wherein the NH.sub.3 decomposing catalyst adsorbs the NH.sub.3 produced by the NH.sub.3 synthesizing catalyst when the engine operating air-fuel ratio is lower than the stoichiometric air-fuel ratio and wherein the NH.sub.3 decomposing catalyst reduces NO.sub.x in the exhaust gas discharged from the engine and pass through the NH.sub.3 synthesizing catalyst when the operating air-fuel ratio of the engine is higher than the stoichiometric air-fuel ratio by reacting the NO.sub.x with the NH.sub.3 component adsorbed in the NH.sub.3 decomposing catalyst.
In this aspect of the invention, the operating air-fuel ratio of the engine fluctuates around the stoichiometric air-fuel ratio. When the engine operating air-fuel ratio is lower than the stoichiometric air-fuel ratio (i.e., rich air-fuel ratio), the NO.sub.x producing catalyst converts the NO.sub.x discharged from the engine to NH.sub.3 and N.sub.2. This NH.sub.3 component is absorbed by the NH.sub.3 decomposing catalyst disposed at downstream of the NH.sub.3 synthesizing catalyst. Therefore, NH.sub.3 is not discharged to atmosphere. When the engine operating air-fuel ratio becomes higher than the stoichiometric air-fuel ratio (i.e., lean air-fuel ratio), the NO.sub.x discharged from the engine pass through the NH.sub.3 synthesizing catalyst without being converted to NH.sub.3 and N.sub.2. However, the NO.sub.x pass through the NH.sub.3 synthesizing catalyst is reduced at the NH.sub.3 decomposing catalyst by reacting the NH.sub.3 absorbed by the NH.sub.3 decomposing catalyst. Therefore, both the NO.sub.x and NH.sub.3 are not discharged to atmosphere.
According to another aspect of the present invention, there is provided a device for resolving NO.sub.x in an exhaust gas of an internal combustion engine, the operating air-fuel ratio of the engine fluctuates around the stoichiometric air-fuel ratio in such a manner that the average operating air-fuel ratio of the engine is higher than the stoichiometric air-fuel ratio, the device comprises an NH.sub.3 synthesizing catalyst disposed on an exhaust gas passage of the engine, wherein the NH.sub.3 synthesizing catalyst converts NO.sub.x in the exhaust gas discharged from the engine when the operating air-fuel ratio of the engine is lower than the stoichiometric air-fuel ratio to NH.sub.3 and N.sub.2, an NO.sub.x absorbent disposed on the exhaust gas passage downstream of the NH.sub.3 synthesizing catalyst, wherein the NO.sub.x absorbent absorbs NO.sub.x in the exhaust gas discharged from the engine and pass through the NH.sub.3 synthesizing catalyst when the operating air-fuel ratio of the engine is higher than the stoichiometric air-fuel ratio and releases the absorbed NO.sub.x when the engine operating air-fuel ratio becomes lower than the stoichiometric air-fuel ratio, and an NH.sub.3 decomposing catalyst disposed on the exhaust gas passage downstream of the NO.sub.x absorbent, wherein, when the engine operating air-fuel ratio is lower than the stoichiometric air-fuel ratio, the NH.sub.3 decomposing catalyst reduces the NO.sub.x released from the NO.sub.x absorbent by reacting the NO.sub.x with the NH.sub.3 produced by the NH.sub.3 synthesizing catalyst.
In this aspect of the invention, the NO.sub.x discharged from the engine when the engine operating air-fuel ratio is higher than the stoichiometric air-fuel ratio are absorbed by the NO.sub.x absorbent. Therefore, the NO.sub.x are not discharged to atmosphere when the engine operating air-fuel ratio is higher than the stoichiometric air-fuel ratio. When the engine operating air-fuel ratio becomes lower than the stoichiometric air-fuel ratio, the NO.sub.x absorbed by the NO.sub.x absorbent are released from the NO.sub.x absorbent. However, the NH.sub.3 synthesizing catalyst converts the NO.sub.x discharged from the engine to NH.sub.3 and N.sub.2 when the engine operating air-fuel ratio becomes lower than the stoichiometric air-fuel ratio. Therefore, the NO.sub.x released from the NO.sub.x absorbent and the NH.sub.3 produced by the NH.sub.3 synthesizing catalyst flows into the NH.sub.3 decomposing catalyst at the same time. These NO.sub.x and NH.sub.3 react each other and form N.sub.2 and H.sub.2 O. Thus, both the NO.sub.x and NH.sub.3 components are not discharged to atmosphere.
According to another aspect of the present invention, there is provided a device for resolving NO.sub.x in an exhaust gas of an internal combustion engine, the operating air-fuel ratio of the engine fluctuates around the stoichiometric air-fuel ratio in such a manner that the average operating air-fuel ratio of the engine is higher than the stoichiometric air-fuel ratio, the device comprising an NH.sub.3 synthesizing catalyst disposed on an exhaust gas passage of the engine, wherein the NH.sub.3 synthesizing catalyst converts NO.sub.x in the exhaust gas discharged from the engine when the operating air-fuel ratio of the engine is lower than the stoichiometric air-fuel ratio of NH.sub.3 and N.sub.2, an NH.sub.3 decomposing catalyst disposed on the exhaust gas passage downstream of the NH.sub.3 synthesizing catalyst, wherein the NH.sub.3 decomposing catalyst absorbs NO.sub.x in the exhaust gas discharged from the engine and pass through the NH.sub.3 synthesizing catalyst when the operating air-fuel ratio of the engine is higher than the stoichiometric air-fuel ratio and wherein the NH.sub.3 decomposing catalyst reduces the absorbed NO.sub.x by reacting the NO.sub.x with the NH.sub.3 produced by the NH.sub.3 synthesizing catalyst when the engine operating air-fuel ratio is lower than the stoichiometric air-fuel ratio.
In this aspect of the invention, the NH.sub.3 decomposing catalyst is also capable of absorbing the NO.sub.x in the exhaust gas flowing into the NH.sub.3 decomposing catalyst when the engine operating air-fuel ratio is higher than the stoichiometric air-fuel ratio. Thus, the NO.sub.x are not discharged to atmosphere when the engine operating air-fuel ratio is higher than the stoichiometric air-fuel ratio. When the engine operating air-fuel ratio becomes lower than the stoichiometric air-fuel ratio, a NH.sub.3 is produced by the NH.sub.3 synthesizing catalyst upstream of the NH.sub.3 decomposing catalyst. However, this NH.sub.3 is oxidized at the NH.sub.3 decomposing catalyst by reacting the NO.sub.x absorbed by the NH.sub.3 decomposing catalyst. Therefore, both the NO.sub.x and NH.sub.3 are not discharged to atmosphere when the engine operating air-fuel ratio becomes lower than the stoichiometric air-fuel ratio.

BRIEF DESCRIPTION OF THE DRAWINGS
The present invention will be better understood from the description, as set forth hereinafter with reference to the accompanying drawings in which:
FIG. 1 is a drawing schematically illustrating an embodiment of the present invention when applied to an automobile engine;
FIG. 2 is a drawing schematically illustrating another embodiment of the present invention;
FIG. 3 is a drawing schematically illustrating another embodiment of the present invention;
FIG. 4 is a drawing schematically illustrating another embodiment of the present invention;
FIG. 5 is a drawing schematically illustrating another embodiment of the present invention;
FIG. 6 is a drawing showing the change in the characteristics of an NH.sub.3 decomposing catalyst in accordance with the change in the temperature; and
FIG. 7 is a drawing schematically illustrating another embodiment of the present invention.

DESCRIPTION OF THE PREFERRED EMBODIMENT
In the embodiments explained hereinafter, NH.sub.3 decomposing catalysts are used for resolving NO.sub.x and NH.sub.3 from a combustion exhaust gas. Therefore, an NH.sub.3 decomposing catalyst is explained before explaining the respective embodiments.
The NH.sub.3 decomposing catalyst in the embodiments of the present invention uses, for example, a honeycomb type substrate made of cordierite, and an alumina layer which act as a carrier for the catalyst is coated on the cell surface of the honeycomb substrate. On this carrier, at least-one substance selected from elements belong to the fourth period or the eighth group in the periodic table of elements, such as copper (Cu), chrome (Cr), vanadium (V), titanium (Ti), iron (Fe), nickel (Ni), cobalt (Co), platinum (Pt), palladium (Pd), rhodium (Rh) and iridium (Ir) are carried as a catalyst.
The NH.sub.3 decomposing catalyst is capable of converting all the NH.sub.3 component in the exhaust gas flowing into the NH.sub.3 decomposing catalyst to the N.sub.2 component provided that the exhaust gas is in an oxidizing atmosphere and the temperature of the catalyst is within a specific temperature range as determined by the substance being used as the catalyst. Therefore, when the exhaust gas is an oxidizing atmosphere containing a NH.sub.3 component and flows through the NH.sub.3 decomposing catalyst in this temperature range, the NH.sub.3 component in the exhaust gas is almost completely resolved, and the exhaust gas flows out from the NH.sub.3 decomposing catalyst contains no NH.sub.3 component. In the explanation below, this temperature range in which the NH.sub.3 decomposing catalyst can resolve all the NH.sub.3 component in the exhaust gas is called an optimum temperature range.
When the temperature of the NH.sub.3 decomposing catalyst is higher than the optimum temperature range, the NH.sub.3 component in the exhaust gas flowing into the NH.sub.3 decomposing catalyst is oxidized by the NH.sub.3 decomposing catalyst and NO.sub.x components are produced.
Namely, when the temperature of the NH.sub.3 decomposing catalyst is higher than the optimum temperature range, the oxidizing reaction of the NH.sub.3 component, i.e., 4NH.sub.3 +7O.sub.2 .fwdarw.4NO.sub.2 +6H.sub.2 O, and/or 4NH.sub.3 +5O.sub.2 .fwdarw.4NO+6H.sub.2 O become dominant on the NH.sub.3 decomposing catalyst, and the amount of NO.sub.x components (mainly NO and NO.sub.2) in the exhaust gas flowing out from the NH.sub.3 decomposing catalyst increases.
Further, when the temperature of the NH.sub.3 decomposing catalyst is lower than the optimum temperature range, the oxidizing reaction of the NH.sub.3 component becomes lower, and the amount of the NH.sub.3 component in the exhaust gas flowing out from the NH.sub.3 decomposing catalyst increases.
FIG. 6 schematically illustrates the change in the characteristics of the NH.sub.3 decomposing catalyst in accordance with the change in the temperature. FIG. 6 shows the change in the concentration of the NH.sub.3 and NO.sub.x components in the exhaust gas flowing out from the NH.sub.3 decomposing catalyst in accordance with the temperature of the NH.sub.3 decomposing catalyst when the exhaust gas flowing into the NH.sub.3 decomposing catalyst is in an oxidizing atmosphere and the concentration of NH.sub.3 in the exhaust gas is maintained at a constant level. The vertical axis and the horizontal axis in FIG. 6 represent the concentration of the respective components in the exhaust gas and the temperature of the NH.sub.3 decomposing catalyst, respectively. The solid line and the dotted line in FIG. 6 represent the concentrations of the NH.sub.3 component and the NO.sub.x components in the exhaust gas flowing out from the NH.sub.3 decomposing catalyst.
As shown in FIG. 6, provided that the concentration of the NH.sub.3 component in the exhaust gas flowing into the NH.sub.3 decomposing catalyst is maintained at a constant level, the concentration of the NH.sub.3 component in the outflow exhaust gas is substantially the same as the concentration of NH.sub.3 in the inflow exhaust gas in the low temperature region (region I, in FIG. 6). In this temperature region, the concentration of the NO.sub.x components in the outflow exhaust gas is substantially zero. This means that substantially all of the NH.sub.3 component in the exhaust gas passes the NH.sub.3 decomposing catalyst without reaction when the temperature is low (region I in FIG. 6).
When the temperature becomes higher than the above low temperature region, the concentration of the NH.sub.3 component in the outflow exhaust gas decreases as the temperature increases, while the concentration of the NO.sub.x components is substantially the same (region II in FIG. 6). Namely, in this temperature region, the amount of NH.sub.3 component in the exhaust gas which is converted to N.sub.2 component increases as the temperature increases.
When the temperature further increases, as shown in region III in FIG. 6, the concentration of NH.sub.3 component in the outflow exhaust gas further decreases and the concentration of both the NH.sub.3 and NO.sub.x components becomes substantially zero. Namely, in this temperature region (region III in FIG. 6), all of the NH.sub.3 component in the exhaust gas flowing into the NH.sub.3 decomposing catalyst is resolved (i.e., converted to N.sub.2 component) by NH.sub.3 decomposing catalyst without forming NO.sub.x components.
However, when the temperature becomes higher than this region, the concentration of the NO.sub.x components in the outflow exhaust gas increases as the temperature increases (region IV in FIG. 6), and all of the NH.sub.3 component in the exhaust gas is converted to NO.sub.x components by the NH.sub.3 decomposing catalyst in a high temperature region (region V in FIG. 6).
In this specification, the optimum temperature range of the NH.sub.3 decomposing catalyst is defined as a temperature range in which all of the NH.sub.3 component in the exhaust gas is converted to N.sub.2 component without forming any NO.sub.x component, i.e., such as the temperature range indicated by the temperature region III in FIG. 6.
The optimum temperature range of the NH.sub.3 decomposing catalyst changes according the substance used as the catalytic component, and generally starts at a relatively low temperature compared with, for example, the activating temperature of the three-way reducing and oxidizing catalyst. For example, when a substance such as platinum (Pt), rhodium (Rh), or palladium (Pd) is used, the optimum temperature range is approximately 100.degree. to 400.degree. C. (preferably 100.degree. to 300.degree. C. and most preferably 100.degree. to 250.degree. C. in case of platinum (Pt), and preferably 150.degree. to 400.degree. C. and most preferably 150.degree. C. to 300.degree. C. in case of rhodium (Rh) or palladium (Pd)). When a substance such as copper (Cu), chrome (Cr), or iron (Fe) (for example) is used, the optimum temperature range is approximately 150.degree. to 650.degree. C. (more preferably, 150.degree. to 500.degree. C.). Therefore, if the NH.sub.3 decomposing catalyst is formed as a tandem compound type catalyst using both types of the catalytic component, i.e., if the catalytic components such as platinum (Pt) are carried on the downstream part of the substrate and the catalytic components such as chrome (Cr) are carried on the upstream part of the substrate, the optimum temperature range of the NH.sub.3 decomposing catalyst can be widened as a whole.
The reason why the NH.sub.3 decomposing catalyst converts substantially all of the NH.sub.3 component in the exhaust gas to the N.sub.2 component without producing any NO.sub.x components only in the specific temperature range is not clear at present. However, it is considered that this phenomenon is due to the following reason.
When the temperature of the NH.sub.3 decomposing catalyst is in the optimum temperature range, the following denitrating reactions occur in the NH.sub.3 decomposing catalyst, in addition to the above mentioned oxidizing reactions 4NH.sub.3 +7O.sub.2 .fwdarw.4NO.sub.2 +6H.sub.2 O and/or 4NH.sub.3 +5O.sub.2 .fwdarw.4NO+6H.sub.2 O:
8NH.sub.3 +6NO.sub.2 .fwdarw.12H.sub.2 O+7N.sub.2
4NH.sub.3 +4NO+O.sub.2 .fwdarw.6H.sub.2 O+4N.sub.2
Due to these denitrating reactions, the NO.sub.x components produced by the oxidizing reactions are immediately converted to the N.sub.2 component. Namely, in the optimum temperature range, a portion of the NH.sub.3 in the exhaust gas flowing into the NH.sub.3 decomposing catalyst is converted to NO.sub.x by the oxidizing reactions, and this NO.sub.x immediately reacts the remaining NH.sub.3 in the exhaust gas and is converted to N.sub.2 by the denitrating reactions. By these sequential reactions, substantially all of the NH.sub.3 in the exhaust gas is converted to N.sub.2 when the temperature of the catalyst is within the optimum temperature range.
When the temperature of the NH.sub.3 decomposing catalyst is above the optimum temperature range, the oxidizing reactions become dominant in the catalyst and the portions of NH.sub.3 which is oxidized by the catalyst increases. Thus, the denitrating reactions hardly occur in the catalyst due to the shortage of NH.sub.3 component in the exhaust gas, and the NO.sub.x produced by the oxidizing reactions flows out from the NH.sub.3 decomposing catalyst without being reduced by the denitrating reactions.
On the other hand, when the temperature of NH.sub.3 decomposing catalyst is below the optimum temperature range, the oxidizing reactions hardly occur due to the low temperature. This causes the NH.sub.3 in the exhaust gas passes through the NH.sub.3 decomposing catalyst without being oxidized by the NO.sub.x due to the shortage of the NO.sub.x in the exhaust gas.
As explained above, the optimum temperature range of the NH.sub.3 decomposing catalyst is a temperature range in which the oxidizing reactions of the NH.sub.3 and the denitrating reactions of the NO.sub.x balance each other in such a manner that the NO.sub.x produced by the oxidation of the NH.sub.3 immediately reacts with NH.sub.3 in the exhaust gas without causing any surplus NO.sub.x and NH.sub.3. Consequently, the optimum temperature range of the NH.sub.3 decomposing catalyst is determined by the oxidizing ability of the catalyst and its temperature dependency. Therefore, when the catalyst component having high oxidizing ability, such as platinum (Pt), is used, the optimum temperature range becomes lower than that when the catalyst component having relatively low oxidizing ability, such as chrome (Cr) is used.
As explained above, though the mechanism of the phenomenon is not completely clarified, the NH.sub.3 decomposing catalyst actually converts all of the NH.sub.3 in the exhaust gas in an oxidizing atmosphere when the temperature is within the optimum temperature range. Further, when the NH.sub.3 decomposing catalyst is used in the optimum temperature range the following facts were found in connection with the above phenomenon:
(a) When the exhaust gas flowing into the NH.sub.3 decomposing catalyst is in an oxidizing atmosphere, i.e., when the air-fuel ratio of the exhaust gas is lean compared to the stoichiometric air-fuel ratio, substantially all of the NH.sub.3 in the exhaust gas is converted to N.sub.2 without producing any NO.sub.x. This occurs when the exhaust gas is in an oxidizing atmosphere (a lean air-fuel ratio), but regardless of the degree of leanness of air-fuel ratio of the exhaust gas. (In this specification, an air-fuel ratio of the exhaust gas at a certain point is defined by a ratio of the air and the fuel which are supplied to the combustion chambers or exhaust passages upstream of the point. Therefore, when no air or fuel is supplied in the exhaust passages upstream of the considered point, the air-fuel ratio of the exhaust gas at the point becomes the same as the air-fuel ratio of the air-fuel mixture supplied to the combustion chambers).
(b) When the exhaust gas flowing into the NH.sub.3 decomposing catalyst contains NO.sub.x in addition to NH.sub.3, all of the NO.sub.x in the exhaust gas as well as the NH.sub.3 is converted to N.sub.2, and the concentration of the NO.sub.x components in the exhaust gas becomes zero. In this case, the ratio of the concentrations of the NO.sub.x components and the NH.sub.3 component is not necessarily stoichiometrical for the denitrating reactions (i.e., 4:3, or 1:1). It is only required that the exhaust gas contains an amount of NH.sub.3 more than the amount required for reducing the NO.sub.x (NO.sub.2 and NO) in the exhaust gas. As explained above, since the surplus NH.sub.3 in the exhaust gas is all converted to N.sub.2 when the exhaust gas is in an oxidizing atmosphere, no surplus NH.sub.3 is contained in the exhaust gas flowing out from the NH.sub.3 decomposing catalyst even in this case.
(c) When the exhaust gas flowing into the NH.sub.3 decomposing catalyst contains HC and CO components, all of the HC and CO components are oxidized by the NH.sub.3 decomposing catalyst, provided that the air-fuel ratio of the exhaust gas is lean compared to the stoichiometric air-fuel ratio, and no HC and CO components are contained in the exhaust gas flowing out from the NH.sub.3 decomposing catalyst.
However, when the exhaust gas flowing into the NH.sub.3 decomposing catalyst contains both the NH.sub.3 and NO.sub.x, it was found that the temperature region IV in FIG. 6, i.e., the temperature region in which the concentration of NO.sub.x components in the outflow exhaust gas increases as the temperature of the catalyst increases, moves to the lower temperature side compared to that when the exhaust gas flowing into the NH.sub.3 decomposing catalyst contains only the NH.sub.3 components. This is because, when the exhaust gas contains NO.sub.x in addition to NH.sub.3, the NO.sub.x in the inflow exhaust gas in addition to the NO.sub.x produced by the oxidizing reaction of NH.sub.3 must be reduced by the NH.sub.3 in the exhaust gas. Consequently, the shortage of the NH.sub.3 is apt to occur in the relatively low temperature region. Therefore, when the exhaust gas contains both the NH.sub.3 and the NO.sub.x, the optimum temperature range of the NH.sub.3 decomposing catalyst becomes narrower.
In relation to above (b), a conventional denitrating catalyst, such as a vanadia-titania (V.sub.2 O.sub.5 -TiO.sub.2) type catalyst also has a capability for resolving NH.sub.3 and NO.sub.x in the exhaust gas under a certain conditions. However, in case of the conventional denitrating catalyst, the amounts of NH.sub.3 and NO.sub.x components must be strictly stoichiometrical in order to react NH.sub.3 with NO.sub.x without causing any surplus NH.sub.3 and NO.sub.x. Namely, when both the NO.sub.2 and NO are contained in the exhaust gas, the amount (moles) of the NH.sub.3 in the exhaust gas must be strictly equal to the total of the moles of NO.sub.2 in the exhaust gas multiplied by 3/4 and the moles of NO in the exhaust gas in order to react NH.sub.3 and NO.sub.x without causing any surplus NH.sub.3 and NO.sub.x. However, in case of the NH.sub.3 decomposing catalyst in the embodiments of the present invention, if the amount of the NH.sub.3 is more than the stoichiometrical compared to the amount of NO.sub.x, and if the air-fuel ratio of the exhaust gas is lean, all of the NH.sub.3 and NO.sub.x are converted to N.sub.2 without causing any surplus NH.sub.3 and NO.sub.x. This is an important difference between the NH.sub.3 decomposing catalyst in the present invention and the conventional denitrating catalyst.
As explained in FIG. 6, though the NH.sub.3 decomposing catalyst converts all of the NH.sub.3 in the exhaust gas in the optimum temperature range, some NH.sub.3 passes through when the temperature is below the optimum temperature range. In order to prevent this outflow of NH.sub.3 in the low temperature region, an acidic inorganic substance may be used. It is known in the art that an acidic inorganic substance (which includes Broensted acids such as zeolite, silica (SiO.sub.2), silica-alumina (SiO.sub.2 -Al.sub.2 O.sub.3), and titania (TiO.sub.2) as well as Lewis acids including oxides of transition metals such as copper (Cu), cobalt (CO), nickel (Ni) and iron (Fe)) absorb NH.sub.3 when the temperature is low. Therefore, one or more of these acidic inorganic substances may be carried on the substrate of the NH.sub.3 decomposing catalyst, or the substrate itself may be formed by a porous material made of such acidic inorganic substances to prevent the outflow of NH.sub.3 in the low temperature region. In this case, the NH.sub.3 component which is not converted to an N.sub.2 component in the lower temperature is absorbed by the acidic inorganic substances in the NH.sub.3 decomposing catalyst, and the amount of the outflow of the NH.sub.3 from the NH.sub.3 decomposing catalyst in the low temperature region can be reduced. The NH.sub.3 absorbed by the acidic inorganic substances are released when the temperature of the NH.sub.3 decomposing catalyst becomes high, or when the concentration of NH.sub.3 component in the exhaust gas becomes low. Therefore, the NH.sub.3 absorbed by the acidic inorganic substance is converted to N.sub.2 by the NH.sub.3 decomposing catalyst when it is released from the acidic inorganic substance. When the temperature of the exhaust gas flowing into the NH.sub.3 decomposing catalyst changes in a wide range, therefore, it is suitable to use these acidic inorganic substances to prevent the outflow Of NH.sub.3 in low temperature region.
Next, embodiments of the present invention which utilizes the NH.sub.3 decomposing catalyst are explained.
FIG. 1 schematically illustrates an embodiment of the present invention when applied to an internal combustion engine. In FIG. 1, reference numeral 1 represents an internal combustion engine, 2 represents an exhaust gas passage of the engine 1. On the exhaust gas passage, a three-way reducing and oxidizing catalyst 3, a muffler 5 and a NH.sub.3 decomposing catalyst 7 are disposed, from the upstream end, in this order. Numeral 9 in FIG. 6 designates a secondary air supply unit which injects air into the exhaust gas passage at the portion between the muffler 5 and NH.sub.3 decomposing catalyst 7.
The three-way reducing and oxidizing catalyst 3 is a known type which uses, for example, a honeycomb type substrate. On this substrate, an alumina layer which acts as a carrier of the catalytic components is applied. In this embodiment, catalytic components of precious metals such as platinum (Pt), palladium (Pd) and rhodium (Rh) and additives such as cerium (Ce) are attached to the alumina carrier. As is well known, the three-way reducing and oxidizing catalyst 3 can resolve HC, CO and NO.sub.x components in the exhaust gas effectively when the air-fuel ratio of the exhaust gas is near the stoichiometric air-fuel ratio. On the other hand, when the air-fuel ratio of the exhaust gas is on a rich side compared to the stoichiometric air-fuel ratio, the three-way reducing and oxidizing catalyst reduces substantially all of NO.sub.x in the exhaust gas, but, in this case, a portion of NO.sub.x in the exhaust gas is converted to NH.sub.3 at the same time. Namely, the three-way reducing and oxidizing catalyst 3 can act as an NH.sub.3 synthesizing catalyst when the air-fuel ratio of the exhaust gas flowing into the catalyst is rich compared to the stoichiometric air-fuel ratio.
The muffler 5 is a conventional type which lowers the sound pressure level by expanding the exhaust gas, and in this embodiment, also used for reducing the temperature of the exhaust gas by expanding it. Further, since the muffler 5 has a relatively large heat capacity, the change in the temperature of the exhaust gas at downstream of the muffler 5 can be kept small even when the temperature of the exhaust gas at upstream of the muffler 5 changes due to the change in the operating conditions of the engine 1 occurs.
As explained before, the NH.sub.3 decomposing catalyst 7 is capable of resolving all of the NH.sub.3 in the exhaust gas when the exhaust gas flowing into the catalyst 7 is in an oxidizing atmosphere and the temperature of the catalyst 7 is within the optimum temperature range. However, when the temperature of the catalyst becomes lower than the optimum temperature range, an outflow of NH.sub.3 occurs. To prevent this outflow of NH.sub.3 in the low temperature region, the acidic inorganic substance may be attached to the substrate of the NH.sub.3 decomposing catalyst or the substrate itself may be formed by a porous material made of the acidic inorganic substance.
The secondary air supply unit 9 includes a pressurized air source 9a such as an air pump, nozzle 10 for injecting air into the exhaust gas passage upstream of the NH.sub.3 decomposing catalyst 7 and a shut off valve 11 disposed on the piping connecting the air source 9a and the nozzle 10. As explained later, a flow control valve which is capable of adjusting the amount of air injected from the nozzle 10 may be used instead of the shut off valve 11.
In this embodiment, the internal combustion engine 1 is operated at an air-fuel ratio near the stoichiometric air-fuel ratio and the air-fuel ratio of the exhaust gas from the engine 1 is usually maintained at the stoichiometric air-fuel ratio. Since the three-way reducing and oxidizing catalyst 3 can resolve the HC, CO and NO.sub.x components in the exhaust gas at a high efficiency when the air-fuel ratio is near the stoichiometric air-fuel ratio, the exhaust gas flowing out from the three-way reducing and oxidizing catalyst 3 usually does not contain any HC, CO and NO.sub.x components. However, even if the operating air-fuel ratio of the engine 1 is maintained near the stoichiometric air-fuel ratio, the air-fuel ratio of the exhaust gas occasionally becomes rich compared to the stoichiometric air-fuel ratio due to the fluctuations of the operating air-fuel ratio of the engine. In such a case, a portion of NO.sub.x in the exhaust gas is converted to NH.sub.3 by the three-way reducing and oxidizing catalyst 3. Thus, the exhaust gas flowing out from the three-way reducing and oxidizing catalyst 3 sometimes contains a small amount of NH.sub.3.
In this embodiment, the NH.sub.3 decomposing catalyst 7 is disposed on the exhaust gas passage downstream of the three-way reducing and oxidizing catalyst 3 in order to resolve the NH.sub.3 formed at the three-way reducing and oxidizing catalyst 3. Namely, the exhaust gas flows out from the three-way reducing and oxidizing catalyst 3 flows down the exhaust gas passage 2 and passes through the muffler 5. Further, air is added to the exhaust gas before it flows into the NH.sub.3 decomposing catalyst 7 by the secondary air supply unit 9.
Usually, the temperature of the exhaust gas at the outlet of the engine 1 is above the optimum temperature range of the NH.sub.3 decomposing catalyst 7. However, the temperature of the exhaust gas becomes lower as the exhaust gas flows down the exhaust gas passage due to the heat dissipation through the wall of the exhaust gas passage 2. Further, when it passes through the muffler 5, the exhaust gas is cooled by the muffler 5. Therefore, the temperature of the exhaust gas when it reaches the NH.sub.3 decomposing catalyst 7 is lower than the temperature at the outlet of the engine 1. In this embodiment, the length of the exhaust gas passage between the engine 1 and the NH.sub.3 decomposing catalyst 7 as well as the capacity of the muffler 5 is determined in such a manner that the temperature of the exhaust gas at the inlet of the NH.sub.3 decomposing catalyst 7 falls in the optimum temperature range even when the engine 1 is operated at the maximum exhaust temperature conditions. By this arrangement, the temperature of the exhaust gas flowing into the NH.sub.3 decomposing catalyst 7, and the temperature of the NH.sub.3 decomposing catalyst 7 accordingly, is always maintained within the optimum temperature range regardless of the change in the operating conditions of the engine 1.
Further, the air-fuel ratio of the exhaust gas flowing into the NH.sub.3 decomposing catalyst 7 is adjusted by supplying air from the secondary air supply unit 9 so that the air-fuel ratio of the exhaust gas becomes lean compared to the stoichiometric air-fuel ratio. As explained before, when the exhaust gas flowing into the NH.sub.3 decomposing catalyst 7 is in an oxidizing atmosphere (i.e., at a lean air-fuel ratio), the NH.sub.3 decomposing catalyst 7 is capable of resolving substantially all of the NH.sub.3 in the exhaust gas regardless of the degree of the leanness of the air-fuel ratio of the exhaust gas. Therefore, it is not necessary to control the amount of air supplied from the secondary air supply unit 9 in order to strictly control the air-fuel ratio of the exhaust gas flowing into the NH.sub.3 decomposing catalyst 7 in this embodiment. The amount of the air supplied from the secondary air supply unit 9 is set at an amount which can keep the air-fuel ratio of the exhaust gas flowing into the NH.sub.3 decomposing catalyst 7 on a lean air-fuel ratio side compared to the stoichiometric air-fuel ratio even when the operating air-fuel ratio of the engine 1 fluctuates to the rich air-fuel ratio side compared to the stoichiometric air-fuel ratio.
By the arrangement explained above, the exhaust gas supplied to the NH.sub.3 decomposing catalyst 7 is always an oxidizing atmosphere and has a temperature within the optimum temperature range. Therefore, even if NH.sub.3 is formed at the three-way reducing and oxidizing catalyst 3, NH.sub.3 is completely resolved by the NH.sub.3 decomposing catalyst 7. Further, when the air-fuel ratio of the exhaust gas becomes rich, the capability of the three-way reducing and oxidizing catalyst 3 for resolving HC and CO component in the exhaust gas decreases. However, according to the present embodiment, HC and CO components passing through the three-way reducing and oxidizing catalyst 3 are also resolved by the NH.sub.3 decomposing catalyst 7. Therefore, according to the present embodiment, an increase in the emission of HC, CO and NH.sub.3 components when the operating air-fuel ratio of the engine fluctuates to rich side can be prevented.
Though the temperature of the exhaust gas is adjusted by the heat dissipation from the wall of the exhaust gas passage 2 and the cooling by the muffler 5 in this embodiment, other means for adjusting the temperature of the exhaust gas may be used. For example, heat radiation fins may be disposed outer wall of the exhaust gas passage 2 instead of, or in addition to the muffler 5, or alternatively, the wall of the exhaust gas passage 2 may be water-cooled to increase the cooling capacity of the exhaust gas passage 2. Further, the amount of the air supplied from the secondary air supply unit 9 may be changed in accordance with the temperature of the exhaust gas to maintain the temperature of the exhaust gas flowing into the NH.sub.3 decomposing catalyst 7 within the optimum temperature range by using a flow control valve instead of the shut off valve 11 in this embodiment. Further, the flow amount of the cooling water for cooling the exhaust gas passage wall, or the amount of the air supplied from the secondary air supply unit may be feedback controlled in accordance with an output signal of a temperature sensor detecting the catalyst bed of the NH.sub.3 decomposing catalyst 7 in such a manner that the temperature of the NH.sub.3 decomposing catalyst is maintained within the optimum temperature range.
In the above embodiment, if the operating air-fuel ratio of the engine 1 fluctuates to a lean air-fuel ratio side compared to the stoichiometric air-fuel ratio, NH.sub.3 is not formed at the three-way reducing and oxidizing catalyst 3, and the capability of the three-way reducing and oxidizing catalyst for reducing NO.sub.x also decreases. In this case, an exhaust gas which contains NO.sub.x, but does not contain NH.sub.3 flows into the NH.sub.3 decomposing catalyst 7. This causes the NO.sub.x in the exhaust gas to pass through the NH.sub.3 decomposing catalyst 7 without being reduced. Therefore, to prevent the emission of the NO.sub.x when the operating air-fuel ratio becomes lean, a NO.sub.x absorbent which is capable of absorbing NO.sub.x in the exhaust gas of a lean air-fuel ratio, or a NO.sub.x reducing catalyst which has a capability for selectively reducing the NO.sub.x in the exhaust gas even in an oxidizing atmosphere may be disposed on the exhaust gas passage 2 between the three-way reducing and oxidizing catalyst 3 and the NH.sub.3 decomposing catalyst 7. FIG. 7 shows an embodiment of the present invention in which a NO.sub.x absorbent or a NO.sub.x reducing catalyst is disposed on the exhaust gas passage 2 between the three-way reducing and oxidizing catalyst 3 and the NH.sub.3 decomposing catalyst 7. In FIG. 7, same reference numerals as those in FIG. 1 represent same elements. Reference numeral 8 in FIG. 7 designates an NO.sub.x absorbent or NO.sub.x reducing catalyst disposed on the exhaust gas passage between the three-way reducing and oxidizing catalyst 3 and the NH.sub.3 decomposing catalyst 7 (in FIG. 7, the NO.sub.x absorbent 8 or the NO.sub.x reducing catalyst is disposed between the three-way reducing and oxidizing catalyst 3 and the muffler 5. However, the NO.sub.x absorbent 8 or the NO.sub.x reducing catalyst may be disposed between the muffler 5 and the NH.sub.3 decomposing catalyst 7). In this embodiment, when the operating air-fuel ratio of the engine fluctuates to lean side, NO.sub.x passes through the three-way reducing and oxidizing catalyst 7 is absorbed by the NO.sub.x absorbent 8 or reduced by the NO.sub.x reducing catalyst 8. Therefore, NO.sub.x is not contained in the exhaust gas flowing into the NH.sub.3 decomposing catalyst 7 even when the operating air-fuel ratio of the engine fluctuates to lean air-fuel ratio side. Though the NO.sub.x absorbent 8 in this embodiment is disposed on the exhaust gas passage 2 separately, it is possible to give the absorbing and releasing capability of NO.sub.x to the substrate of the NH.sub.3 decomposing catalyst. This is accomplished by attaching the NO.sub.x absorbing substances (explained later) to the substrate of the NH.sub.3 decomposing catalyst 7 in addition to the catalytic components.
The NO.sub.x absorbent and the NO.sub.x reducing catalyst will be explained later in detail.
Next, another embodiment of the present invention is explained. Though the engine 1 in the previous embodiment is operated near the stoichiometric air-fuel ratio, the engine in this embodiment is operated at a slightly rich air-fuel ratio in such a manner that an excess air ratio .lambda. falls in the range between 0.95 and 0.98. Since the construction of the device of the present embodiment is the same as that of the previous embodiment, the present embodiment is also explained with reference to FIG. 1.
In the previous embodiment, the operating air-fuel ratio of the engine 1 fluctuates to the lean air-fuel ratio side as well as to the rich air-fuel ratio side due to the change in the operating conditions. When the operating air-fuel ratio of the engine becomes lean, the NO.sub.x components in the exhaust gas pass through the three-way reducing and oxidizing catalyst 3 without being reduced. Further, since the three-way reducing and oxidizing catalyst 3 does not produce NH.sub.3 when the air-fuel ratio of the exhaust gas is lean, the NH.sub.3 decomposing catalyst 7 cannot resolve the NO.sub.x components in the exhaust gas. To prevent this, the engine 1 in this embodiment is operated at slightly rich air-fuel ratio so that the operating air-fuel ratio does not become lean compared to the stoichiometric air-fuel ratio even when the operating air-fuel ratio of the engine 1 fluctuates to some extent.
Since the engine 1 is operated at a rich air-fuel ratio in normal operation, NH.sub.3 is formed at the three-way reducing and oxidizing catalyst 3 during the normal operation of the engine 1, and the amounts of the HC, CO components in the exhaust gas also increases in the normal operation of the engine 1 in this embodiment. However, the NH.sub.3 formed at the three-way reducing and oxidizing catalyst 3 and the HC, CO components passes through the three-way reducing and oxidizing catalyst 3 are both resolved by the NH.sub.3 decomposing catalyst 7 in this embodiment. Therefore, the emission of NH.sub.3, as well as HC and CO, does not occur in this embodiment. As explained above, according to the present embodiment, the emission of the NH.sub.3, HC and CO components are reduced by operating the engine 1 at a slightly rich air-fuel ratio.
Next, another embodiment is explained with reference to FIG. 2.
In FIG. 2, the same reference numerals as those in FIG. 1 represent the same elements. The embodiment in FIG. 2 is different from the embodiment in FIG. 1 in that an NO.sub.x absorbent 8 is disposed on the exhaust gas passage 2 downstream of the NH.sub.3 decomposing catalyst 7. The NO.sub.x absorbent 8 absorbs NO.sub.x in the exhaust gas when the air-fuel ratio of the exhaust gas is lean compared to the stoichiometric air-fuel ratio. The NO.sub.x absorbent 8 in this embodiment uses, for example, alumina as a carrier and, on this carrier, precious metals such as platinum (Pt) rhodium (Rh), and at least one substance selected from alkali metals such as potassium (K), sodium (Na), lithium (Li) and cesium (Cs); alkali-earth metals such as barium (Ba) and calcium (Ca); and rare-earth metals such as lanthanum (La) and yttrium (Y) is carried. The NO.sub.x absorbent 8 absorbs NO.sub.x in the exhaust gas when the air-fuel ratio of the exhaust gas is lean, and releases the absorbed NO.sub.x when the oxygen concentration of the exhaust gas flowing the NO.sub.x absorbent becomes lower.
Though the mechanism of this absorption and releasing operation of the NO.sub.x absorbent is not clear at present, it is considered that the absorption and releasing operation is conducted by the following mechanism. Though the following mechanism of the absorption and the releasing operation of the NO.sub.x absorbent is explained for the case where platinum Pt and barium (Ba) are carried on the carrier, as an example, it is considered that a similar mechanism also applies even if other precious metal, alkali metals, alkali earth metals, or rare earth metals are used.
Namely, when the concentration of O.sub.2 in the exhaust gas increases, i.e., when the air-fuel ratio of the exhaust gas becomes lean, the oxygen O.sub.2 in the exhaust gas is deposited on the surface of platinum (Pt) in the form of O.sub.2 - or O.sup.2+. The NO in the exhaust gas reacts with O.sub.2 - or O.sup.2- on the surface of the platinum (Pt) and becomes NO.sub.2 (2NO+O.sub.2 .fwdarw.2NO.sub.2). Then, NO.sub.2 in the exhaust gas and the NO.sub.2 produced on the platinum (Pt) are further oxidized on the surface of platinum (Pt) and absorbed into the NO.sub.x absorbent while bonding with the barium oxide (BaO) and diffusing in the absorbent in the form of nitric acid ions NO.sub.3 -. Thus, NO.sub.x in the exhaust gas is absorbed by the NO.sub.x absorbent 8 when the air-fuel ratio of the exhaust gas is lean.
On the other hand, when the oxygen concentration in the exhaust gas becomes low, i.e., when the air-fuel ratio of the exhaust gas becomes rich, the production of NO.sub.2 on the surface of the platinum (Pt) is lowered and the reaction proceeds in an inverse direction (NO.sub.3 -.fwdarw.NO.sub.2), and thus nitric acid ions NO.sub.3 - in the absorbent are released in the form of NO.sub.2 from the NO.sub.x absorbent 8.
In this case, if the reducing substance such as NH.sub.3 and CO, or the substance such as HC and CO.sub.2 exist in the exhaust gas, the released NO.sub.x is reduced on the platinum Pt by these components. Namely, the NO.sub.x absorbent 8 performs the absorbing and releasing operation of the NO.sub.x in the exhaust gas in which the NO.sub.x in the exhaust gas is absorbed by the NO.sub.x absorbent when the air-fuel ratio of the exhaust gas is lean and released from the NO.sub.x absorbent when the air-fuel ratio of the exhaust gas becomes rich.
As explained in FIG. 6, the NH.sub.3 decomposing catalyst 7 converts the NH.sub.3 in the exhaust gas to NO.sub.x when the temperature becomes higher than the optimum temperature range. Therefore, if the exhaust gas temperature at the outlet of the engine 1 becomes very high in an extreme operating condition of the engine 1, the temperature maintaining means such as the muffler 5 might be insufficient to lower the exhaust gas temperature to the optimum temperature range of the NH.sub.3 decomposing catalyst 7. In such a case, since the temperature of the exhaust gas flowing into the NH.sub.3 decomposing catalyst 7 exceeds the optimum temperature range, NO.sub.x is formed at the NH.sub.3 decomposing catalyst 7 and is discharged to atmosphere.
In this embodiment, the NO.sub.x absorbent 8 is disposed on the exhaust gas passage 2 downstream of the NH.sub.3 decomposing catalyst 7 to prevent the emission of the NO.sub.x in the extremely high exhaust gas temperature conditions. Since the NO.sub.x absorbent 8 absorbs the NO.sub.x in the exhaust gas in an oxidizing atmosphere, the NO.sub.x formed at the NH.sub.3 decomposing catalyst 7 in the extremely high exhaust gas temperature condition is absorbed by the NO.sub.x absorbent 8 and the emission of the NO.sub.x to the atmosphere does not occur.
As explained above, according to the present embodiment, the exhaust emission can be always kept low even when the exhaust gas temperature becomes extremely high.
Though the NO.sub.x absorbent 8 in the above embodiment is disposed on the exhaust gas passage 2 separately, it is possible to give the absorbing and releasing capability of NO.sub.x to the substrate of the NH.sub.3 decomposing catalyst. This is accomplished by attaching the NO.sub.x absorbing substances such as alkali metals and alkali-earth metals to the substrate of the NH.sub.3 decomposing catalyst 7 in addition to the catalytic components.
Next, another embodiment of the present invention is explained. In this embodiment, an NO.sub.x reducing catalyst is disposed on the exhaust gas passage downstream of the NH.sub.3 decomposing catalyst 7 instead of the NO.sub.x absorbent 8 in FIG. 2. Other constructions of this embodiment are the same as those in FIG. 2. Therefore, illustration of this embodiment by drawings is omitted.
The NO.sub.x reducing catalyst in this embodiment has a substrate made of, for example, zeolite ZSM-5, and metals such as copper (Cu) and iron (Fe) are attached to the substrate by an ion exchange method. Alternatively, a substrate made of zeolite such as mordenite and precious metal such as platinum (Pt) attached thereon can also be used as the NO.sub.x reducing catalyst. The NO.sub.x reducing catalyst traps NH.sub.3, HC and CO components in the exhaust gas in the pores of the porous zeolite, and selectively reduces the NO.sub.x in the exhaust gas using these trapped components even in an oxidizing atmosphere.
In this embodiment, the NO.sub.x reducing catalyst disposed at downstream of the NH.sub.3 decomposing catalyst 7 in FIG. 2 traps the NH.sub.3 component in the exhaust gas which passes through the NH.sub.3 decomposing catalyst 7 when the exhaust gas temperature is below the optimum temperature range as well as the HC and CO components in the exhaust gas. Further, when the exhaust gas temperature is above the optimum temperature range, the NO.sub.x reducing catalyst selectively reduces the NO.sub.x formed at the NH.sub.3 decomposing catalyst 7 using the trapped NH.sub.3, HC and CO components. Therefore, according to the present embodiment, the NO.sub.x formed at the NH.sub.3 decomposing catalyst in the high exhaust gas temperature conditions is not emitted to atmosphere and the exhaust emissions are always maintained at low level regardless of the change in the operating conditions of the engine.
Next another embodiment of the present invention is explained with reference to FIG. 3. In FIG. 3, the same reference numerals as those in FIG. 1 designate the same elements.
In this embodiment, means for cooling the exhaust gas such as the muffler 5 in FIG. 1 is not used. Further, a plurality of the NH.sub.3 decomposing catalyst are disposed on the exhaust gas passage 2 downstream of the three-way reducing and oxidizing catalyst 3 (FIG. 3 shows the case in which three NH.sub.3 decomposing catalyst 7a to 7c are used). Also, the secondary air supply unit 9 in this embodiment has a plurality of the nozzles 10a to 10c which are each disposed, in the exhaust gas passage 2, at the inlet of the respective NH.sub.3 decomposing catalysts 7a to 7c. Reference numeral 30 in FIG. 3 designates a control circuit of the engine 1. The control circuit 30 may be comprises, for example, a micro-computer of known type and performs basic controls of the engine 1 such as a fuel infection control and an ignition timing control. In this embodiment, the control circuit 30 also act as selecting means which selects the nozzles of the secondary air supply unit 9 in accordance with the exhaust gas temperature discharged from the engine 1 to supply air to the NH.sub.3 decomposing catalysts which is in the optimum temperature range. To perform these controls, signals representing the operating condition of the engine 1 such as the inlet air flow amount and the speed of the engine 1 are fed to the control circuit 30 from the respective sensors not shown in the drawing. Further, the control circuit 30 is connected to shut off valves 11a to 11c which are disposed on the piping connecting the pressurized air source 9a and the respective nozzles 10a to 10c to control the operation of these shut off valves.
The temperature of the exhaust gas becomes lower as it flows down the exhaust gas passage 2 due to the heat dissipation through the passage wall during the operation of the engine 1. Since plural NH.sub.3 decomposing catalysts are disposed on the exhaust gas passage 2 in series in this embodiment, the temperature of the exhaust gas flowing into the respective NH.sub.3 decomposing catalysts are different. Therefore, the temperature of the respective NH.sub.3 decomposing catalysts are also different from each other in this embodiment. Further, the length of the exhaust gas passage 2 between the engine 1 and the respective NH.sub.3 decomposing catalysts are determined in such a manner that the temperature of at least one NH.sub.3 decomposing catalysts falls in the optimum temperature range throughout the whole operating range of the engine 1. Namely, at least one NH.sub.3 decomposing catalyst is maintained at a temperature within the optimum temperature range in this embodiment regardless of the change in the operating conditions of the engine 1.
During the operation of the engine 1, the control circuit 30 determines the temperature of the respective NH.sub.3 decomposing catalysts based on the operating conditions of the engine, and supplies air to the NH.sub.3 decomposing catalyst(s) which has a temperature within the optimum temperature range by activating the shut off valve connected to the nozzle at the inlet of that NH.sub.3 decomposing catalyst(s). Thus, secondary air is supplied only to the NH.sub.3 decomposing catalyst(s) which has a temperature within the optimum temperature range. The temperature of the respective NH.sub.3 decomposing catalysts change in accordance with the temperature of the exhaust gas at the outlet of the engine 1 (i.e., the engine load) and the amount of the exhaust gas flow (i.e., the engine speed). In this embodiment, the temperature of the respective NH.sub.3 decomposing catalysts are previously measured using the actual engine under various engine loads and speed conditions, and the NH.sub.3 decomposing catalysts to which air is supplied (i.e., the NH.sub.3 decomposing catalysts having a temperature within the optimum temperature range) are determined previously in accordance with the engine load and speed and stored in the memory of the control circuit 30. The control circuit 30 determines the NH.sub.3 decomposing catalysts to which the air should be supplied, in accordance with the engine load and speed during the engine operation, and opens the shut off valves connected to the air nozzles at the inlet of those NH.sub.3 decomposing catalysts.
Therefore, according to the present embodiment, the NO.sub.x and the NH.sub.3 in the exhaust gas are effectively resolved regardless of the change in the exhaust gas temperature at the outlet of the engine by using the NH.sub.3 decomposing catalyst which has the temperature within the optimum temperature range. Further, it is known that the catalytic components of the NH.sub.3 decomposing catalyst which are precious metals such as platinum (Pt), rhodium (Rh) and palladium (Pd) also act as three-way reducing and oxidizing catalyst when the temperature is higher than the optimum temperature range. Therefore, these precious metal catalytic components may be used for the NH.sub.3 decomposing catalysts located upstream (for example, NH.sub.3 decomposing catalysts 7a and 7b in FIG. 3). In this case, the upstream NH.sub.3 decomposing catalysts act as supplementary three-way reducing and oxidizing catalysts when the temperature of the upstream NH.sub.3 decomposing catalysts are higher than the optimum temperature range, and the NH.sub.3 and NO.sub.x in the exhaust gas are resolved by the NH.sub.3 decomposing catalysts located downstream.
Though three NH.sub.3 decomposing catalysts are used in the present embodiment, the number of the NH.sub.3 decomposing catalysts is not limited to three, i.e., two or more NH.sub.3 decomposing catalysts may be used in accordance with the type of the engine and the arrangement of the exhaust gas system. Further, the catalytic components used for the NH.sub.3 decomposing catalysts may be the same for all the NH.sub.3 decomposing catalysts, or different components for respective NH.sub.3 decomposing catalysts may be used. Further, means for cooling the exhaust gas such as the muffler 5 used in the embodiment in FIG. 1 can be used also in this embodiment to lower the exhaust gas temperature.
Further, though the control circuit 30 selects the NH.sub.3 decomposing catalysts having a temperature within the optimum temperature range based on the operating condition of the engine 1, the NH.sub.3 decomposing catalyst may be selected based on the actual temperature measured by temperature sensors disposed on the exhaust gas passage at the inlet of the respective NH.sub.3 decomposing catalysts, or by temperature sensors disposed on the catalyst beds of the respective NH.sub.3 decomposing catalysts.
Next, another embodiment of the present invention is explained with reference to FIG. 4. In the embodiments explained above, the present invention is applied to the system in which the internal combustion engine is operated at the air-fuel ratio near the stoichiometric air-fuel ratio, or lower than the stoichiometric air-fuel ratio (i.e., the rich air-fuel ratio). However, in this embodiment, the present invention is applied to an engine operated at an air-fuel ratio higher than the stoichiometric air-fuel ratio (i.e., a so-called lean burn engine).
In FIG. 4, reference numeral 41 designates an lean burn engine which is operated at an air-fuel ratio higher than the stoichiometric air-fuel ratio, 42 designates an exhaust gas passage of the engine 41. A muffler 45 and a NH.sub.3 decomposing catalyst 47 which are similar to the muffler 5 and the NH.sub.3 decomposing catalyst 7 in FIG. 1, respectively, are disposed on the exhaust gas passage 42. However, a three-way reducing and oxidizing catalyst 3 as shown in FIG. 5 is not provided in this embodiment. Further, instead of the secondary air supply unit 9 in FIG. 1, an NH.sub.3 supply unit 49 which comprises a nozzle 50 and a shut off valve 51 which are similar to those in FIG. 1 and a NH.sub.3 supply source 49a such as a bottle containing gaseous or liquid NH.sub.3 is provided in this embodiment.
In this embodiment, the exhaust gas in an oxidizing atmosphere from the lean burn engine 41 is cooled by the muffler 45 and flows into the NH.sub.3 decomposing catalyst 47 at the temperature within the optimum temperature range Further, NH.sub.3 is added to the exhaust gas at the portion upstream of the NH.sub.3 decomposing catalyst 47. The exhaust gas from the lean burn engine 41 contains a relatively large amount of NO.sub.x. Thus, the exhaust gas flowing into the NH.sub.3 decomposing catalyst is adjusted so that it becomes an oxidizing atmosphere and a temperature within the optimum temperature range. Further, the exhaust gas contains NO.sub.x and NH.sub.3. Therefore, both the NO.sub.x and the NH.sub.3 in the exhaust gas are completely resolved by the NH.sub.3 decomposing catalyst 47.
As explained before, the capability of the three-way reducing and oxidizing catalyst for reducing the NO.sub.x becomes very small when the exhaust gas is in an oxidizing atmosphere. Therefore, it is difficult to resolve the NO.sub.x in the exhaust gas of the lean burn engine using the three-way reducing and oxidizing catalyst. However, according to the present invention, the NO.sub.x in the exhaust gas from the lean burn engine can be completely resolved by the NH.sub.3 decomposing catalyst 47.
Further, the method for resolving NO.sub.x in the exhaust gas of in an oxidizing atmosphere by adding an NH.sub.3 component to the exhaust gas and using a conventional vanadia-titania (V.sub.2 O.sub.5 -TiO.sub.2) type denitrating catalyst is known in the art. In the above conventional method, NO.sub.x and NH.sub.3 are converted to N.sub.2 and H.sub.2 O by the denitrating reactions (8NH.sub.3 +6NO.sub.2 .fwdarw.12H.sub.2 O+7N.sub.2 and/or 4NH.sub.3 +4NO.sub.2 +O.sub.2 .fwdarw.6H.sub.2 O+4N.sub.2). However, in the conventional method, the amount of NO.sub.x components and the NH.sub.3 component must be adjusted so that the ratio of the moles of NO.sub.x and NH.sub.3 are strictly stoichiometrical (i.e., 4:3 or 1:1) in order to react NO.sub.x with NH.sub.3 without causing any surplus NO.sub.x and NH.sub.3, as explained before.
However, in the actual operation of the engine, the concentration of the NO.sub.x components in the exhaust gas varies widely in accordance with the operating condition of the engine, and it is difficult to control the amount of the NH.sub.3 added to the exhaust gas in accordance with the concentration of the NO.sub.x in the exhaust gas. Therefore, if the conventional method is used for an actual engine, NO.sub.x or NH.sub.3 is emitted to the atmosphere in some cases.
However, in case of the NH.sub.3 decomposing catalyst 47 in this embodiment, it is not required to strictly control the amount of the NH.sub.3 added to the exhaust gas since the NH.sub.3 decomposing catalyst can convert all of the NH.sub.3 in the exhaust gas as long as the exhaust gas is in an oxidizing atmosphere. In this embodiment, it is only required that the amount of the NH.sub.3 added to the exhaust gas is sufficiently large to reduce all of the NO.sub.x in the exhaust gas while maintaining the exhaust gas in an oxidizing atmosphere. Therefore, according to the present embodiment, the NO.sub.x in the exhaust gas of the lean burn engine can be completely resolved by a simple control of the NH.sub.3 supply unit 49 while preventing the emission of NH.sub.3.
FIG. 5 shows another embodiment of the present invention which is similar to the embodiment in FIG. 3. In this embodiment, a plurality of the NH.sub.3 decomposing catalysts (47a to 47c in FIG. 5) and NH.sub.3 supply nozzles (50a to 50c in FIG. 5) are disposed on the exhaust gas passage 42. Similarly to the embodiment in FIG. 3, the control circuit 30 selects the NH.sub.3 decomposing catalyst which is in the optimum temperature range according to the operating conditions of the engine 41, and supplies NH.sub.3 to those NH.sub.3 decomposing catalysts through the NH.sub.3 nozzle located at the inlet of those NH.sub.3 decomposing catalysts. Since the operation of the present embodiment is substantially the same as the operation of the embodiment in FIG. 3, a detailed explanation is not given here.
From the description set forth above, it will be understood that, according to the present invention, the NH.sub.3 and NO.sub.x components contained in the combustion exhaust gas can be resolved effectively by the NH.sub.3 decomposing catalyst. Though the present invention is explained using the embodiments in which the present invention is applied to the internal combustion engine, the application of the present invention is not limited to the internal combustion engine. The present invention can be also applied to resolve the NH.sub.3 and NO.sub.x components in the exhaust gas discharged from the combustion devices other than the internal combustion engine. Namely, the present invention can be also applied to, for example, boilers, furnaces etc., which emit combustion exhaust gases.

Number	Date	Country	Kind
7-011903	Jan 1995	JPX
7-280797	Oct 1995	JPX

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5120695	Blumrich et al.	Jun 1992
5292991	Lachman et al.	Mar 1994
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5433071	Willey et al.	Jul 1995

Number	Date	Country
A-0701858	Mar 1996	EPX
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60-143833	Jul 1985	JPX
63-236522	Oct 1988	JPX
4-265122	Sep 1992	JPX
4-365920	Dec 1992	JPX
6190246A	Jul 1994	JPX

Method for purifying combustion exhaust gas

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