EXHAUST PURIFICATION SYSTEM OF INTERNAL COMBUSTION ENGINE

Abstract

An exhaust purification system of an internal combustion engine includes an NOX storage reduction catalyst device which is arranged in an engine exhaust passage. The NO storage reduction catalyst device stores SOX simultaneously with NOX. When the stored SOX amount exceeds a predetermined allowable amount, the SOX is made to be released by SOX release control which raises the temperature of the NOX catalyst device to the SOX releasable temperature, then makes the air-fuel ratio of the exhaust gas which flows into the NOX catalyst device the stoichiometric air-fuel ratio or rich. The NOX catalyst device has a residual SOX storage amount which finally remains even if performing SOX release control depending on the temperature of the NOX catalyst device when performing SOX release control. The system uses the residual SOX storage amount of the current SOX release control as the basis to calculate the SOX release speed at each timing in the current SOX release control.

Description

TECHNICAL FIELD

The present invention relates to an exhaust purification system of an internal combustion engine.

BACKGROUND ART

The exhaust gas of diesel engines, gasoline engines, and other internal combustion engines includes, for example, carbon monoxide (CO), unburned fuel (HC), nitrogen oxides (NO_X), particulate matter (PM), and other constituents. The internal combustion engines are mounted with exhaust purification systems for removing these constituents.

As one method for removing nitrogen oxides, arrangement of an NO_X storage reduction catalyst in an engine exhaust passage has been proposed. The NO_X storage reduction catalyst stores NO_X when the air-fuel ratio of the exhaust gas is lean. When the storage amount of the NO_X reaches an allowable amount, the air-fuel ratio of the exhaust gas may be made rich or the stoichiometric air-fuel ratio so that the stored NO_X is released. The released NO_X is reduced to N₂ by the carbon monoxide or other reducing agent which is contained in the exhaust gas.

Japanese Patent Publication (A) No. 2000-314311 discloses a purification system arranging a purification catalyst of nitrogen oxides in an exhaust gas flow path of the internal combustion engine. The nitrogen oxide purification catalyst has a precious metal and a nitrogen oxide trapping material. It is disclosed that the nitrogen oxide purification catalyst can trap nitrogen oxides as NO₂ by a higher air-fuel ratio than the stoichiometric air-fuel ratio. Further, the trapping material of nitrogen oxides traps SO_X, but it is disclosed that by rendering the atmosphere a reducing one, the trapped SO_X can be removed. Further, it is disclosed that the temperature for removing the trapped SO_X is preferably 500° C. or more.

The exhaust gas of an internal combustion engine sometimes contains sulfur oxides (SO_X). An NO_X storage reduction catalyst stores SO_X at the same time as storing NO_X. If SO_X is stored, the storable amount of NO_X falls. In this way, the NO_X storage reduction catalyst suffers from so-called “sulfur poisoning”. To eliminate sulfur poisoning, sulfur poisoning recovery treatment is performed for releasing the SO_X. In the sulfur poisoning recovery treatment, the NO_X storage reduction catalyst is raised in temperature and, in that state, the air-fuel ratio of the exhaust gas is made rich or the stoichiometric air-fuel ratio to release the SO_X.

At the time of sulfur poisoning recovery treatment of the Na_X storage reduction catalyst, the SO_X is released into the atmosphere. If the release speed of the SO_X is large, a large amount of SO_X ends up being released in a short time, so odor and other problems arise.

On the other hand, an NO_X storage reduction catalyst suffers from thermal degradation. If thermal degradation occurs, for example, the NO_X storable amount is decreased. Thermal degradation proceeds faster the higher the temperature of the NO_X storage reduction catalyst. When performing sulfur poisoning recovery treatment, the temperature elevated state continues for a long time. For this reason, at the time of sulfur poisoning recovery treatment, thermal degradation proceeds relatively fast.

In the prior art, the target temperature and the regeneration time of the NO_X storage reduction catalyst are set in advance. During this regeneration time, the sulfur poisoning recovery treatment was performed while maintaining the target temperature. Alternatively, the SO_X release speed may be detected by using a map using the fuel injection amount and temperature etc. in the combustion chambers as functions. The SO_X release amount can be calculated from the SO_X release speed. However, the SO_X release speed which is detected by the prior art includes relatively large error. For this reason, at the time of sulfur poisoning recovery treatment, there was a possibility that the NO_X storage reduction catalyst would be exposed to a higher temperature atmosphere than required and that thermal degradation would excessively proceed. The SO_X release speed when performing sulfur poisoning recovery treatment preferably can be precisely detected.

DISCLOSURE OF INVENTION

The present invention has as its object the provision of an exhaust purification system of an internal combustion engine including an NO_X storage reduction catalyst device, which exhaust purification system of an internal combustion engine can precisely calculate an SO_X release speed when performing sulfur poisoning recovery treatment.

The exhaust purification system of an internal combustion engine of the present invention arranges in an engine exhaust passage an NO_X catalyst device which stores NO_X which is contained in exhaust gas when an air-fuel ratio of the inflowing exhaust gas is lean and which releases the stored NO_X when the air-fuel ratio of the inflowing exhaust gas becomes a stoichiometric air-fuel ratio or rich and which uses SO_X release control which raises a temperature of the NO_X catalyst device to an SO_X releasable temperature when an SO_X amount which is stored in the NO_X catalyst device exceeds a predetermined allowable amount and which makes the air-fuel ratio of the exhaust gas which flows into the NO_X catalyst device a stoichiometric air-fuel ratio or rich so as to make the stored SO_X be released. The NO_X catalyst device has a residual SO_X storage amount which is dependent on the temperature of the NO_X catalyst device when performing SO_X release control and finally remains even if performing SO_X release control. The system uses the residual SO_X storage amount of the current SO_X release control as the basis to calculate the SO_X release speed at each timing in the current SO_X release control. By adopting this configuration, the system precisely calculate the SO_X release speed when performing SO_X release control.

In the above invention, preferably, in the current SO_X release control, the system uses a difference between a SO_X storage amount at each timing and the residual SO_X storage amount as the basis to calculate the SO_X release speed at each timing.

In the above invention, preferably the system uses the SO_X release speed which was calculated at each timing of the SO_X release control as the basis to calculate a cumulative SO_X release amount which is released from the start of SO_X release control to the current timing and corrects the calculated SO_X release speed at the current timing based on a ratio of a first radius and a second radius where when a releasable SO_X amount obtained by subtracting from an SO_X storage amount when starting SO_X release control the residual SO_X storage amount is deemed to correspond to an area of a circle of the first radius, a radius of a circle of an area corresponding to the cumulative SO_X release amount is calculated as the second radius.

In the above invention, preferably the NO_X catalyst device has a final NO_X storable amount at which NO_X can be stored when the residual SO_X storage amount remains, and the system uses the SO_X release speed which was calculated at each timing of the SO_X release control as the basis to calculate an NO_X recovery amount which is restored from the start of SO_X release control to the current timing and corrects the calculated SO_X release speed at the current timing based on a ratio of a first radius and a second radius where when a restorable NO_X storable amount obtained by subtracting from the final NO_X storable amount an NO_X storable amount when starting SO_X release control is deemed to correspond to an area of a circle of the first radius, a radius of a circle of an area corresponding to the NO_X recovery amount is calculated as the second radius.

In the above invention, preferably the system uses the SO_X release speed which was calculated at each timing of the SO_X release control as the basis to calculate a cumulative SO_X release amount which is released from the start of SO_X release control to the current timing and corrects the calculated SO_X release speed at the current timing based on a ratio of a first radius and a second radius where when a releasable SO_X amount obtained by subtracting from an SO_X storage amount when starting SO_X release control the residual SO_X storage amount is deemed to correspond to a volume of a sphere of the first radius, a radius of a sphere of a volume corresponding to the cumulative SO_X release amount is calculated as the second radius.

In the above invention, preferably the NO_X catalyst device has a final NO_X storable amount at which storage of NO_X is possible when the residual SO_X storage amount remains, and the system uses an SO_X release speed which was calculated at the each timing of SO_X release control as the basis to calculate a NO_X recovery amount which is restored from the start of SO_X release control to the current timing and corrects the calculated SO_X release speed at the current timing based on a ratio of a first radius and a second radius where when a restorable NO_X storable amount obtained by subtracting from the final NO_X storable amount an NO_X storable amount when starting SO_X release control is deemed to correspond to a volume of a sphere of the first radius, a radius of a sphere of a volume corresponding to the NO_X recovery amount is calculated as the second radius.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 is a schematic view of an internal combustion engine in Embodiment 1.

FIG. 2 is an enlarged schematic cross-sectional view of an NO_X storage reduction catalyst device when storing NO_X.

FIG. 3 is an enlarged cross-sectional view of an NO_X storage reduction catalyst device when storing SO_X.

FIG. 4 is a map of an SO_X storage amount per unit time as a function of the engine speed and the demanded torque.

FIG. 5 is a time chart for when performing sulfur poisoning recovery treatment.

FIG. 6 is a graph which explains a relationship between an SO_X amount which is stored in an NO_X storage reduction catalyst device and a SO_X release speed in Embodiment 1.

FIG. 7 is a graph of a bed temperature of an NO_X storage reduction catalyst device and a finally remaining residual SO_X storage amount in Embodiment 1.

FIG. 8 is a view which explains changes in an SO_X amount which is stored in an NO_X storage reduction catalyst device in SO_X release control.

FIG. 9 is a flow chart for when performing SO_X release control in Embodiment 1.

FIG. 10 is a graph of a case of using a correction term to calculate an SO_X release speed in Embodiment 1 and a comparative example which calculates an SO_X release speed without using a correction term.

FIG. 11 is an enlarged schematic view which explains a state where SO_X is released at a high temperature from an NO_X storage reduction catalyst device.

FIG. 12 is an enlarged schematic view which explains a state where SO_X is released at a low temperature from an NO_X storage reduction catalyst device.

FIG. 13 is a schematic view which explains an SO_X release model.

FIG. 14 is a graph of an SO_X release speed when using a calculated correction term for calculation in Embodiment 2.

FIG. 15 is a flow chart for when performing SO_X release control in Embodiment 2.

FIG. 16 is a view which explains a change of an NO_X storable amount of an NO_X storage reduction catalyst device in SO_X release control.

FIG. 17 is a graph which explains a relationship between a temperature of an NO_X storage reduction catalyst device and a final NO_X storable amount for when unreleasable SO_X remains in Embodiment 3.

FIG. 18 is a graph which explains a relationship between an SO_X storage amount and an NO_X storable amount in Embodiment 3.

BEST MODE FOR CARRYING OUT INVENTION

Embodiment 1

Referring to FIG. 1 to FIG. 10, an exhaust purification system of an internal combustion engine in Embodiment 1 will be explained. The internal combustion engine in the present embodiment is arranged in a vehicle. In the present embodiment, the explanation will be given with reference to a compression ignition type diesel engine mounted in a vehicle as an example.

FIG. 1 shows an overall view of the internal combustion engine in the present embodiment. The internal combustion engine is provided with an engine body 1. Further, the internal combustion engine is provided with an exhaust purification system which purifies exhaust gas. The engine body 1 includes cylinders constituted by combustion chambers 2, electronic control type fuel injectors 3 for injecting fuel into the combustion chambers 2, an intake manifold 4, and an exhaust manifold 5.

The intake manifold 4 is connected through an intake duct 6 to an outlet of a compressor 7a of an exhaust turbocharger 7. An inlet of the compressor 7a is connected through an intake air detector 8 to an air cleaner 9. Inside the intake duct 6, a throttle valve 10 which is driven by a step motor is arranged. Furthermore, around the intake duct 6, a cooling device 11 is arranged for cooling the intake air which flows through the inside of the intake duct 6. In the embodiment shown in FIG. 1, the engine cooling water is guided to the cooling device 11. The engine cooling water is used to cool the intake air.

The exhaust manifold 5 is connected to the inlet of an exhaust turbine 7b of the exhaust turbocharger 7. The exhaust purification system in the present embodiment is provided with an NO_X catalyst device comprised of an NO_X storage reduction catalyst device (NSR) 17 (hereinafter simply referred to as an “NO_X storage reduction catalyst”). The NO_X storage reduction catalyst 17 is connected to an outlet of the exhaust turbine 7b through an exhaust pipe 12. Downstream of the NO_X storage reduction catalyst 17 inside of the engine exhaust passage, a particulate filter 16 is arranged for trapping particulate in the exhaust gas. Further, downstream of the particulate filter 16 inside of the engine exhaust passage, an oxidation catalyst 13 is arranged.

Between the exhaust manifold 5 and the intake manifold 4, an EGR passage 18 is arranged for performing exhaust gas recirculation (EGR). Inside the EGR passage 18, an electronic control type EGR control valve 19 is arranged. Further, around the EGR passage 18, a cooling device 20 is arranged for cooling the EGR gas which flows through the inside of the EGR passage 18. In the embodiment shown in FIG. 1, engine cooling water is guided into the cooling device 20. The engine cooling water is used to cool the EGR gas.

The fuel injectors 3 are connected through fuel feed tubes 21 to a common rail 22. The common rail 22 is connected through an electronic control type variable discharge fuel pump 23 to a fuel tank 24. The fuel which is stored in the fuel tank 24 is supplied by a fuel pump 23 to the inside of the common rail 22. The fuel which is supplied to the inside of the common rail 22 is supplied through the fuel feed tubes 21 to the fuel injectors 3.

The electronic control unit 30 is comprised of a digital computer. The electronic control unit 30 in the present embodiment functions as a control system of the exhaust purification system. The electronic control unit 30 includes constituents which are connected to each other by a bidirectional bus 31 such as a ROM (read only memory) 32, RAM (random access memory) 33, CPU (microprocessor) 34, input port 35, and output port 36.

The ROM 32 is a read only storage device. The ROM 32 stores in advance maps and other information necessary for control. The CPU 34 can perform any computation or judgment. The RAM 33 is a random access storage device. The RAM 33 stores the operating history and other information or temporarily stores results of processing.

Downstream of the NO_X storage reduction catalyst 17, a temperature sensor 26 is arranged for detecting the temperature of the NO_X storage reduction catalyst 17. Downstream of the oxidation catalyst 13, a temperature sensor 27 is arranged for detecting the temperature of the oxidation catalyst 13 or particulate filter 16. At the particulate filter 16, a differential pressure sensor 28 is attached for detecting the differential pressure before and after the particulate filter 16. The output signals of these temperature sensors 26 and 27, differential pressure sensor 28, and intake air detector 8 are input through the corresponding AD converters 37 to the input port 35.

An accelerator pedal 40 is connected to a load sensor 41 which generates an output voltage proportional to the amount of depression of the accelerator pedal 40. The output voltage of the load sensor 41 is input through a corresponding AD converter 37 to the input port 35. Furthermore, the input port 35 is connected to a crank angle sensor 42 which generates an output pulse every time the crankshaft rotates by for example 15°. The output of the crank angle sensor 42 can be used to detect the speed of the engine body 1.

On the other hand, the output port 36 is connected through corresponding drive circuits 38 to the fuel injectors 3, the step motor for driving the throttle valve 10, the EGR control valve 19, and the fuel pump 23. In this way, the fuel injector 3 and throttle valve 10 etc. are controlled by the electronic control unit 30.

The oxidation catalyst 13 is a catalyst which has an oxidation ability. The oxidation catalyst 13 is, for example, provided with a substrate which has partition walls extending in the flow direction of the exhaust gas. The substrate is, for example, formed in a honeycomb structure. The substrate is for example housed in a tubular case. On the surface of the substrate, for example, a porous oxide powder is used to form a coated layer serving as a catalyst carrier. The coated layer carries a catalyst metal formed by platinum (Pt), rhodium (Rd), palladium (Pd), or other such precious metal. The carbon monoxide or unburned hydrocarbons which are contained in the exhaust gas are oxidized at the oxidation catalyst and converted to water, carbon dioxide, etc.

The particulate filter 16 is a filter for removing carbon particles, sulfates and other ion-based particles, and other particulates contained in the exhaust gas. The particulate filter, for example, has a honeycomb structure and has a plurality of channels extending in the flow direction of the gas. In the plurality of channels, channels with downstream ends which are sealed and channels with upstream ends which are sealed are alternately formed. The partition walls of the channels are formed by cordierite or other such porous material. When the exhaust gas passes through these partition walls, the particulate is trapped.

The particulate matter is trapped and oxidized on the particulate filter 16. The particulate matter which gradually deposits on the particulate filter 16 is removed by oxidation by raising the temperature in an excess air atmosphere to for example 600° C. or so.

FIG. 2 is an enlarged schematic cross-sectional view of an NO_X storage reduction catalyst. The NO_X storage reduction catalyst 17 is a catalyst which temporarily stores the NO_X which is contained in the exhaust gas which is discharged from the engine body 1 and converts the stored NO_X to N₂ when releasing it.

The NO_X storage reduction catalyst 17 is comprised of a substrate on which for example a catalyst carrier 45 comprised of alumina is carried. On the surface of the catalyst carrier 45, a catalyst metal 46 formed by a precious metal is carried dispersed. On the surface of the catalyst carrier 45, a layer of an NO_X absorbent 47 is formed. As the catalyst metal 46, for example, platinum Pt is used. As the ingredient forming the NO_X absorbent 47, for example, at least one element selected from potassium K, sodium Na, cesium Cs, or other such alkali metal, barium Ba, calcium Ca, or other alkali earth, lanthanum La, yttrium Y, or other such rare earth is used. In the present embodiment, as the ingredient forming the NO_X absorbent 47, barium Ba is used.

In the present invention, the ratio of the air and fuel (hydrocarbons) in the exhaust gas which is supplied to the engine intake passage, combustion chambers, or engine exhaust passage is referred to as the “air-fuel ratio of the exhaust gas (A/F)”. When the air-fuel ratio of the exhaust gas is lean (when it is larger than the stoichiometric air-fuel ratio), the NO which is contained in the exhaust gas is oxidized on the catalyst metal 46 and becomes NO₂. The NO₂ is stored in the form of nitrate ions NO₃⁻ in the NO_X absorbent 47. As opposed to this, when the air-fuel ratio of the exhaust gas is rich or when it becomes the stoichiometric air-fuel ratio, the nitrate ions NO₃⁻ which are stored in the NO_X absorbent 47 are released in the form of NO₂ from the NO_X absorbent 47. The released NO_X is reduced to N₂ by the unburned hydrocarbons, carbon monoxide, etc. contained in the exhaust gas.

FIG. 3 shows another enlarged schematic cross-sectional view of an NO_X storage reduction catalyst. Exhaust gas contains SO_X, that is, SO₂. If SO₂ flows into the NO_X storage reduction catalyst 17, it is oxidized at the catalyst metal 46 and becomes SO₃. This SO₃ is absorbed at the NO_X absorbent 47 and for example generates sulfate BaSO₄. Sulfate BaSO₄ is stable and hard to break down. If just making the air-fuel ratio of the exhaust gas rich, the sulfate BaSO₄ remains as it is without being broken down. For this reason, the NO_X amount which the NO_X storage reduction catalyst can store falls. In this way, the NO_X storage reduction catalyst suffers from sulfur poisoning.

To recover from sulfur poisoning, the temperature of the NO_X storage reduction catalyst is raised to a temperature where SO_X can be released. In this state, SO_X release control is performed to make the air-fuel ratio of the exhaust gas which flows into the NO_X storage reduction catalyst rich or the stoichiometric air-fuel ratio. By performing this SO_X release control, it is possible to make the NO_X storage reduction catalyst release SO_X.

In the present embodiment, at the time of ordinary operation of the internal combustion engine, the SO_X amount which is stored in the NO_X storage reduction catalyst is calculated. The SO_X storage amount is calculated continuously during operation of the internal combustion engine. The exhaust purification system in the present embodiment is provided with a detection device for the SO_X storage amount during ordinary operation. Referring to FIG. 1, the detection device for the SO_X storage amount in the present embodiment includes an electronic control unit 30.

FIG. 4 shows a map of the SO_X amount which is stored per unit time in the NO_X storage reduction catalyst as a function of the engine speed and the demanded torque. By specifying the engine speed N and the demanded torque TQ, it is possible to find the SO_X amount SOXZ which is stored in the NO_X storage reduction catalyst per unit time. This map is stored in for example the ROM 32 of the electronic control unit 30. The operation is continued and, every predetermined time period, the SO_X amount which is stored per unit time is found from the map. The SO_X storage amount is for example stored in the RAM 33. It is possible to consider the SO_X storage amount which remains at the time of the end of the previous sulfur poisoning recovery treatment and cumulatively add the calculated SO_X storage amount so as to detect the SO_X storage amount at any timing.

The detection device of the SO_X amount which is stored during ordinary operation is not limited to this mode. It is possible to employ any device which can detect the SO_X amount which is stored in the NO_X storage reduction catalyst.

FIG. 5 shows a time chart for when performing sulfur poisoning recovery treatment. At the timing t₀, the SO_X storage amount of the NO_X storage reduction catalyst reaches the allowable value. From the timing t₀, the sulfur poisoning recovery treatment is started. Temperature elevation control is performed to raise the temperature of the NO_X storage reduction catalyst from the timing t₀. Referring to FIG. 1, the temperature elevation control is, for example, performed by controlling the fuel injectors 3 which inject fuel into the combustion chambers 2. In the combustion chambers 2, it is possible to retard the injection timing of the main injection performed near compression top dead center so as to make the temperature of the exhaust gas rise. Furthermore, by performing after-injection as auxiliary injection at a time at which fuel can be burned after main injection, it is possible to make the temperature of the exhaust gas rise. By the temperature of the exhaust gas rising, the NO_X storage reduction catalyst can be raised in temperature.

At the timing t_s the bed temperature of the NO_X storage reduction catalyst reaches the target temperature at which SO_X can be released. SO_X release control is performed from the timing t_s. In the SO_X release control of the present embodiment, the bed temperature of the NO_X storage reduction catalyst is maintained at a substantially constant temperature. Furthermore, in the SO_X release control, the air-fuel ratio of the exhaust gas which flows into the NO_X storage reduction catalyst is made the stoichiometric air-fuel ratio or rich.

In the present embodiment, the injection amount of the after injection is increased to make the air-fuel ratio of the exhaust gas the stoichiometric air-fuel ratio or rich. At this time, the throttle valve 10 which is arranged at the engine intake passage may also be choked. Alternatively, by performing post-injection as auxiliary injection at a time at which fuel cannot be burned after the main injection, the air-fuel ratio of the exhaust gas can be made the stoichiometric air-fuel ratio or rich. The “post-injection” is injection which is performed after the injection timing of the after-injection. By making the air-fuel ratio of the exhaust gas which flows into the NO_X storage reduction catalyst the stoichiometric air-fuel ratio or rich, the SO_X can be made to be released.

The device which raises the temperature of the NO_X storage reduction catalyst and the device which controls the air-fuel ratio of the exhaust gas which flows into the NO_X storage reduction catalyst are not limited to this mode. Any device may be employed.

At the timing t_e, the SO_X storage amount reaches the judgment value for ending the SO_X release control. At the timing t_e, the SO_X release control is ended and the sulfur poisoning recovery treatment is ended.

When performing SO_X release control, the speed by which SO_X is released from the NO_X storage reduction catalyst is expressed by the following formula. The SO_X release speed R becomes a function of the temperature T, the SO_X storage amount S of the current timing, and the reducing agent CO which flows into the NO_X storage catalyst. The reducing agent includes unburned fuel and carbon monoxide.

R=f(T,S,CO)  (1)

The SO_X release speed R can, for example, be specifically expressed by the following formula. The next formula applies the Arrhenius equation.

R=A×exp(−E_a/RT)×[SO_X][CO]  (2)

Here, the coefficient A is a frequency factor and is a physical value. A can be found experimentally. The constant E_a is the activation energy and is a known physical property. The variable T is the absolute temperature. The coefficient R is the gas constant. The variable [SO_X] shows the concentration of sulfates. The variable [CO] shows the concentration of the reducing agent which flows into the NO_X storage reduction catalyst.

Formula (2) shows that for example the higher the temperature, the greater the SO_X release speed becomes and that the greater the SO_X storage amount, the greater the SO_X release speed becomes. Furthermore, this shows that the greater the amount of the reducing agent, the greater the SO_X release speed.

The inventors discovered that even if performing sulfur poisoning recovery treatment, sometimes it is not possible to make all of the SO_X which is stored in the NO_X storage reduction catalyst be released. In the present invention, the SO_X amount which finally remains even if performing sulfur poisoning recovery treatment is called the “residual SO_X storage amount”.

FIG. 6 is a graph which explains the relationship between the SO_X storage amount and SO_X release speed of the NO_X storage reduction catalyst. The abscissa shows the SO_X storage amount of the NO_X storage reduction catalyst, while the ordinate shows the SO_X release speed. FIG. 6 shows an example of performing SO_X release control at a bed temperature of the NO_X storage reduction catalyst of 650° C., 620° C., or 580° C. It is learned that the greater the SO_X storage amount, the larger the SO_X release speed.

It is learned that when the bed temperature of the NO_X storage reduction catalyst is 650° C., the SO_X release speed is larger than zero until the SO_X storage amount becomes substantially zero. That is, when the bed temperature of the NO_X storage reduction catalyst is 650° C., it is possible to release substantially all of the stored SO_X. As opposed to this, as the bed temperature of the NO_X storage reduction catalyst becomes lower, cases appear where the SO_X release speed becomes zero despite SO_X remaining at the NO_X storage reduction catalyst. In this way, at a predetermined temperature or less, even if performing SO_X release control, SO_X remains at the NO_X storage reduction catalyst

FIG. 7 shows the relationship between the bed temperature of the NO_X storage reduction catalyst and the residual SO_X storage amount. The abscissa shows the bed temperature of the NO_X storage reduction catalyst when performing SO_X release control. The ordinate shows the residual SO_X storage amount which finally remains even if performing SO_X release control. When the temperature of the NO_X storage reduction catalyst is low, the residual SO_X storage amount becomes larger. As the temperature of the NO_X storage reduction catalyst becomes higher, the residual SO_X storage amount becomes smaller. In this way, the inventors clarified that sometimes SO_X is not completely released and remains at the NO_X storage reduction catalyst. Further, the inventors clarified that the residual SO_X storage amount depends on the temperature of the NO_X storage reduction catalyst when performing SO_X release control.

FIG. 8 schematically shows the SO_X amount which remains at the NO_X storage reduction catalyst when performing SO_X release control. The timing t_s is the timing when starting SO_X release control. The timing t_e is the timing of ending the SO_X release control. In the present embodiment, the time when the SO_X storage amount becomes the residual SO_X storage amount is made the end timing t_e. The timing t₁ is any timing when performing SO_X release control.

The total NO_X storable amount Q_total is the maximum amount of NO_X which the NO_X storage reduction catalyst can store. The NO_X storage reduction catalyst stores NO_X and stores SO_X. At the timing t_s, the NO_X storage reduction catalyst stores the initial SO_X storage amount S₀ of SO_X. By performing SO_X release control, SO_X is released. The SO_X storage amount S_t1 at the timing t₁ becomes smaller than the initial SO_X storage amount S₀. In the present embodiment, the system detects when the SO_X storage amount reaches the residual SO_X storage amount S_e and ends SO_X release control.

In the present embodiment, the system precisely detects the amount of SO_X which is released from the NO_X storage reduction catalyst, that is, the SO_X release amount. It precisely detects the timing t_e when the SO_X storage amount S_t1 of the NO_X storage reduction catalyst becomes the residual SO_X storage amount S_e.

In the present embodiment, when performing SO_X release control, the system calculates the SO_X release speed at every predetermined interval. It is possible to multiply the calculated SO_X release speed with predetermined intervals to calculate the SO_X amount which is released at predetermined intervals. By cumulatively adding the calculated SO_X release amount, it is possible to calculate the cumulative SO_X release amount M_t1 from the start of the SO_X release control to any timing. It is possible to subtract from the initial SO_X storage amount S₀ the cumulative SO_X release amount M_t1 to thereby calculate the SO_X storage amount S_t1 at any timing.

In the present embodiment, the system considers the finally remaining residual SO_X storage amount S_e to calculate the SO_X release speed. In the present embodiment, when calculating the SO_X release speed R, the SO_X storage amount S_t1 of the NO_X storage reduction catalyst is used to calculate the SO_X storage amount S_t1* when corrected by the following formula (3):

S _t1 *=S _t1×(1−S_e/S_t1=S_t1−S_e  (3)

For example, in the formula (1) or formula (2), the SO_X storage amount S_t1* after correction is entered instead of the SO_X storage amount S_t1 so as to calculate the SO_X release speed at the current timing. That is, the SO_X release speed R_t1 at the timing t₁ can be expressed by the following formula by modifying the formula (1).

R _t1 =f(T_t1,S_t1*,CO_t1)  (4)

In this way, the difference between the SO_X storage amount at each timing and the residual SO_X storage amount can be used as the basis to calculate the SO_X release speed at each timing.

FIG. 9 is a flow chart of the time when performing SO_X release control in the present embodiment. When the SO_X amount which is stored in the NO_X storage reduction catalyst exceeds the allowable value, the sulfur poisoning recovery treatment is started. Temperature elevation control is performed, then, at step 101, SO_X release control is started.

Next, at step 102, the residual SO_X storage amount S_e is detected. First, the temperature of the NO_X storage reduction catalyst is detected. Referring to FIG. 1, the temperature of the NO_X storage reduction catalyst 17 can be detected, for example, by a temperature sensor 26 which is arranged downstream of the NO_X storage reduction catalyst 17. As explained above, the residual SO_X storage amount depends on the temperature. The exhaust purification system of an internal combustion engine in the present embodiment is provided with a map of the residual SO_X storage amount as a function of the temperature of the NO_X storage reduction catalyst. The map of the residual SO_X storage amount is, for example, stored in the ROM 32 of the electronic control unit 30. The temperature of the NO_X storage reduction catalyst 17 and map are used to detect the residual SO_X storage amount S_e.

Next, at step 103, the SO_X storage amount S_t1 at the current timing t₁ is read. Right after the SO_X release control is started, the initial SO_X storage amount S₀ which is stored in the NO_X storage reduction catalyst becomes the SO_X storage amount S_t1 of the current timing.

Next, at step 104, to calculate the SO_X release speed, the corrected SO_X storage amount S_1t is calculated. The SO_X storage amount S_t1 at the timing t₁ and the residual SO_X storage amount S_e can be used to calculate the SO_X storage amount S_t1* after correction by the formula (3).

Next, at step 105, the SO_X storage amount S_t1* after correction is used to calculate the SO_X release speed R_t1, at the timing t₁ by, for example, formula (4).

Alternatively, when using the formula (2) to calculate the SO_X release speed, it is possible to find the concentration of sulfates [SO_X] from the SO_X storage amount S_t1* after correction so as to calculate the SO_X release speed R_t1. The concentration [CO] of the reducing agent can for example be calculated from the amount of fuel which is injected into the combustion chambers, the intake air flow amount, the temperature of the exhaust gas, etc.

Next, at step 106, the SO_X release amount ΔM_t during a micro time Δt is calculated.

ΔM_t=R_t1×Δt  (5)

The micro time Δt used may be any time. The micro time Δt is the length of the interval for calculating the SO_X release speed. The micro time Δt is the time from when calculating the SO_X release speed to when calculating the next SO_X release speed.

Next, at step 107, the current SO_X storage amount is reduced by the SO_X release amount ΔM_t of the micro time Δt so as to calculate the new SO_X storage amount.

Next, at step 108, it is judged if the calculated SO_X storage amount S_t1 is the residual SO_X storage amount S_e or less. When the SO_X storage amount S_t1 becomes larger than the residual SO_X storage amount S_e, the routine returns to step 103 where this calculation is repeated. In this way, it is possible to calculate the SO_X storage amount S_t1 at any timing t₁.

At step 108, when the SO_X storage amount S_t1 is the residual SO_X storage amount S_e or less, the routine proceeds to step 109 where the SO_X release control is ended. In this way, the fact of the SO_X storage amount reaching the residual SO_X storage amount is detected.

FIG. 10 shows a graph of the SO_X release speed which is calculated by the method of calculation in the present embodiment and a graph of a comparative example where the calculation is performed without considering the residual SO_X storage amount. Further, FIG. 10 shows the points of examples measuring the SO_X release speed by experiments.

In the comparative example, the calculation is performed without correction of the SO_X storage amount S_t1 shown in formula (3). In the graph of the comparative example, there is an SO_X release speed until the SO_X storage amount of the NO_X storage reduction catalyst becomes zero. As opposed to this, in the example of calculation in the present embodiment, if the SO_X storage amount of the NO_X storage reduction catalyst becomes the residual SO_X storage amount, the SO_X release speed becomes zero. It is learned that the examples of calculation of the present embodiment match with the actually measured values well.

In the present embodiment, the residual SO_X storage amount of the current SO_X release control is used as the basis to calculate the SO_X release speed at each timing in the current SO_X release control. By adopting this configuration, when performing SO_X release control, the remaining SO_X is considered and the SO_X release speed can be calculated precisely. In particular, in the present embodiment, the difference between the SO_X storage amount at each timing in the current SO_X release control and the residual SO_X storage amount is used as the basis to calculate the SO_X release speed at each timing. Due to this configuration it is possible to calculate the SO_X release speed precisely by simple control.

Further, in the present embodiment, to calculate the SO_X release speed at each timing, it is possible to precisely calculate the SO_X release amount from the NO_X storage reduction catalyst. Alternatively, it is possible to precisely calculate the SO_X storage amount which remains at the NO_X storage reduction catalyst. It is possible to precisely judge the end timing of the SO_X release control. As result, it is possible to avoid the time for SO_X release control becoming longer than necessary. It is possible to suppress thermal degradation of the NO_X storage reduction catalyst. Alternatively, it is possible to avoid fuel being consumed more than necessary when performing auxiliary injection at the combustion chambers.

In the present embodiment, the SO_X release control is ended when the SO_X storage amount becomes the residual SO_X storage amount, but the invention is not limited to this mode. It is possible to make the SO_X release control end at any SO_X storage amount.

Further, the formula for calculating the SO_X release speed is not limited to the formula (2). It is possible to apply the correction term of the formula (3) in the present embodiment to any formula (1) for calculating the SO_X release speed. Further, the correction of the SO_X release speed is not limited to the mode. It is possible to employ any correction considering the residual SO_X storage amount.

The sulfur poisoning recovery treatment is performed each time the SO_X amount which is stored in the NO_X storage catalyst increases and reaches the allowable value. When performing the sulfur poisoning recovery treatment a plurality of times, the temperature of the NO_X storage reduction catalyst at the time when performing the SO_X release control may be changed each time.

Embodiment 2

Referring to FIG. 1, FIG. 6, FIG. 8, and FIG. 11 to FIG. 15, an exhaust purification system of an internal combustion engine in Embodiment 2 will be explained. In the present embodiment, the formula for calculating the SO_X release speed is used corrected.

Referring to FIG. 6, the SO_X release speed is decreased in accordance with a decrease of the SO_X storage amount of the NO_X storage catalyst. It is learned that the trend of decrease of the SO_X release speed at this time differs according to the bed temperature of the NO_X storage reduction catalyst. For example, when the bed temperature of the NO_X storage reduction catalyst is 650° C., the graph of the SO_X release speed becomes substantially linear. In this regard, if the bed temperature of the NO_X storage reduction catalyst becomes lower, the graph of the SO_X release speed becomes curved. When the bed temperature of the NO_X storage reduction catalyst is low, there is the trend that after the release of SO_X is started, the SO_X release speed rapidly decreases, then the SO_X release speed gradually decreases. In the present embodiment, a correction term for calculating this trend is incorporated into the formula for calculating the SO_X release speed.

FIG. 11 is an enlarged schematic view of an NO_X storage reduction catalyst in the present embodiment. FIG. 11 is an enlarged schematic view of when performing SO_X release control until the SO_X storage amount becomes the residual SO_X storage amount. The NO_X storage reduction catalyst contains the catalyst metal 46. SO_X 50 is contained in the NO_X absorbent in the form of sulfate. If performing SO_X release control, near the catalyst metal 46, a large amount of SO_X 50 is released. In this regard, at a position a predetermined distance from the catalyst metal 46, a large amount of SO_X 50 remains. It is learned that along with the distance from the catalyst metal 46, the remaining SO_X gradually increases.

FIG. 12 shows another enlarged schematic view of an NO_X storage reduction catalyst in the present embodiment. FIG. 12 is an enlarged schematic view of the time when performing SO_X release control at a lower temperature than the temperature of the NO_X storage reduction catalyst in FIG. 11. By rendering the bed temperature of the NO_X storage reduction catalyst a low temperature to perform the SO_X release control, the SO_X 50 which is released is decreased. Even near the catalyst metal 46, SO_X 50 remains. In the case of this example as well, it is learned that the along with the distance from the catalyst metal 46, the remaining SO_X gradually increases.

Referring to FIG. 11 and FIG. 12, it is learned that if performing SO_X release control, SO_X is released centered about the catalyst metal 46. Further, it is learned that the distance from the catalyst metal 46 at which SO_X is completely released becomes longer the higher the temperature of the NO_X storage reduction catalyst. In this way, it is learned that the higher the temperature of the NO_X storage reduction catalyst, the more possible it is to release SO_X at a position distant from the catalyst metal 46. In the present embodiment, the distance from the catalyst metal 46 is used to create a model of release of SO_X.

FIG. 13 shows a schematic view of a model of the release of SO_X. In the first release model in the present embodiment, circles are defined centered about the catalyst metal 46. The areas of the circles are deemed to correspond to the SO_X release amount.

A circle of a first radius of a radius r₁ is defined centered about the catalyst metal 46. Further, a circle of a second radius of a radius r₂ is defined centered about the catalyst metal 46. In this release model, the release of the SO_X proceeds from the catalyst metal 46 toward the outside. The inside of the circle of the radius r₁ centered about the catalyst metal 46 corresponds to the region where the SO_X can be released. The outside of the circle of the radius r₁ centered about the catalyst metal 46 corresponds to the region where SO_X cannot be released and SO_X remains. The radius r₁ depends on the bed temperature of the NO_X storage reduction catalyst when performing SO_X release control. The inside of the circle of the radius r₂ is a region releasing SO_X up to any timing. The radius r₂ gradually becomes larger as the SO_X release control proceeds. The radius r₂ can become larger up to the radius r₁.

When considering the release model of FIG. 13, the concentration of the sulfate BaSO₄ which can be involved in the reduction reaction is calculated by the following formula:

[BaSO₄]*=[BaSO₄](1−r₂/r₁)  (6)

The concentration of sulfates is multiplied with the correction term (1−r₂/r₁) to calculate the concentration of sulfates after correction. Similarly, the SO_X release speed R_t1* after correction is expressed by the following formula using the SO_X release speed R_t1 before correction.

R _t1 *=R _t1×(1−r₂/r₁)  (7)

Formula (7) shows that as the radius r₂ approaches the radius r₁, the SO_X release speed approaches zero. That is, this shows that as the SO_X storage amount S_t1 approaches the residual SO_X storage amount S_e, the SO_X release speed approaches zero. Further, the formula (7) shows that even with the same value of the radius r₂, if the radius r₁ is large, the SO_X release speed R_t1* after correction becomes larger. That is, this shows that even if the SO_X storage amount S_t1 is the same, if the NO_X storage reduction catalyst is a high temperature, the SO_X release speed R_t1* after correction becomes larger. Further, this shows that the SO_X release speed R_t1* after correction decreases linearly along with a decrease of the SO_X storage amount when the radius r₁ is large.

Next, the ratio of the radius r₁ and the radius r₂ included in the formula (7) is calculated. In the first release model, the SO_X release amount is made to correspond to the area of the circle shown in FIG. 13. That is, the SO_X release amount is given by the following formula:

πr²∝SO_X release amount  (8)

Referring to FIG. 8 and FIG. 13, the area of the circle of the radius r₁ corresponds to the releasable SO_X amount (final SO_X release amount) M_e. The releasable SO_X amount M_e is the value of the SO_X storage amount S₀ when starting the SO_X release control minus the residual SO_X storage amount S_e. Further, the area of the circle of the radius r₂ corresponds to the cumulative SO_X release amount M_t1 which is released from the timing t, to the timing t₁. It is possible to use formula (8) to calculate the radius r₁.

πr₁²∝M_e  (9)

πr₁²=kM_e(k:constant)

r ₁=(k/π×M_e)^1/2  (10)

Next, in the same way as deriving the radius r₁, the formula (8) may be used to calculate the radius r₂.

πr₂²∝M_t1  (11)

πr₂²=kM_t1(k:constant)

r ₂=(k/π×M_t1)^1/2  (12)

From formula (10) and formula (12), the ratio of the radius r₁ and the radius r₂ can be calculated by the following formula:

r ₂ /r ₁=(M_t1/M_e)^1/2  (13)

In this way, the ratio of the radius r₁ and the radius r₂ can be calculated from the releasable SO_X amount M_e and the cumulative SO_X release amount M_t1 which is released from the timing t_s to the timing t₁. Furthermore, it is possible to enter the value calculated by the formula (13) into the formula (7) so as to calculate the SO_X release speed R_t1* after correction.

R _t1 *=R _t1×(1−(M_t1/M_e)^1/2  (14)

FIG. 14 shows a graph of the results of calculations performed by the first release model of the present embodiment. The abscissa shows the SO_X storage amount of the NO_X storage reduction catalyst, while the ordinate shows the SO_X release speed. When the SO_X storage amount is large, a trend is shown where the SO_X release speed greatly decreases along with the decrease of the SO_X storage amount. If the SO_X storage amount becomes smaller, a trend is shown where the SO_X release speed decreases slightly along with the decrease of the SO_X storage amount. Further, the higher the bed temperature of the NO_X storage reduction catalyst, the greater this trend and the more curved the graph shown.

In this way, in the first release model, the calculated SO_X release speed may be corrected based on the radius r₁ and radius r₂ so as to precisely calculate the SO_X release speed.

FIG. 15 shows a flow chart for when performing the SO_X release control in the present embodiment. At step 101, the SO_X release control is started. At step 102, the residual SO_X storage amount S_e is detected. Step 101 and step 102 are similar to Embodiment 1.

Next, at step 111, the initial SO_X storage amount S₀ is reduced by the residual SO_X storage amount S_e to calculate the releasable SO_X amount M_e (see FIG. 8). Next, at step 103, the SO_X storage amount S_t1 at the current timing t₁ is detected.

Next, at step 112, the detected SO_X storage amount S_t1 is used to calculate the SO_X release speed R_t1 before correction by the formula (1). Further, at step 113, the initial SO_X storage amount S₀ is reduced by the SO_X storage amount S_t1 at the timing t₁ to calculate the cumulative SO_X release amount M_t1.

Next, at step 114, the SO_X release speed R_t1* after correction is calculated. The releasable SO_X amount M_e and the cumulative SO_X release amount M_u can be used to calculate the SO_X release speed R_t1* after correction by the above formula (14).

Next, at step 115, the SO_X release speed R_t1* after correction is used to calculate the SO_X release amount (ΔM_t) of the micro time Δt. Next, at step 107, the current SO_X storage amount may be reduced by the released SO_X amount to calculate a new SO_X storage amount. Step 107 to step 109 are similar to Embodiment 1.

In this way, in the present embodiment, it is possible to use the SO_X release speed after correction to calculate the SO_X release amount to thereby calculate a more accurate SO_X release amount. Alternatively, it is possible to precisely calculate the SO_X storage amount which is stored in the NO_X storage catalyst.

Next, the second release model in the present embodiment will be explained. In the second release model in the present embodiment, a sphere is defined centered about the catalyst metal 46. That is, the range of release of SO_X defined in the first release model is made not a circle, but a sphere. In the second release model, the SO_X release amount is deemed to correspond to the volume of the sphere. That is, the SO_X release amount is given by the following formula:

(4/3)πr³∝SO_X release amount  (15)

In the second release model, the volume of the sphere of the first radius comprised of the radius r₁ corresponds to the releasable SO_X amount M_e. The volume of the sphere of the second radius comprised of the radius r₂ corresponds to the cumulative SO_X release amount M_t1 which was released from the timing t_s to the timing t₁. The formula (15) is used to derive the following formulas:

(4/3)πr₁³=kM_e(k:constant)  (16)

(4/3)πr₂³=kM_t1(k:constant)  (17)

From formula (16) and formula (17), the ratio of the radius r₁ and the radius r₂ can be calculated by the following formula:

r ₂ /r ₁=(M_t1/M_e)^1/3  (18)

The ratio of the radius r₁ and the radius r₂ can be calculated by the releasable SO_X amount M_e and the cumulative SO_X release amount M_t1 which was released from the timing t_s to the timing t₁. Furthermore, formula (18) may be entered into the formula (7) so as to calculate the SO_X release speed R_t1* after correction.

R _t1 *=R _t1×(1−(M_t1/M_e)^1/3)  (19)

In the second release model as well, the calculated SO_X release speed may be corrected based on the radius r₁ and the radius r₂ to precisely calculate the SO_X release speed. Further, the corrected formula of the SO_X release speed may be used to calculate the SO_X release amount to enable more accurate calculation of the SO_X release amount. Alternatively, it is possible to precisely calculate the SO_X storage amount which is stored in the NO_X storage catalyst.

The rest of the configuration, action, and effects are similar to those of Embodiment 1, so the explanations will not be repeated here.

Embodiment 3

Referring to FIG. 1, FIG. 7, FIG. 8, and FIG. 16 to FIG. 18, an exhaust purification system of an internal combustion engine in Embodiment 3 will be explained. In the present embodiment, the correction term of the SO_X release speed which was explained in Embodiment 2 is calculated using the NO_X storable amount of the NO_X storage reduction catalyst. That is, the ratio of the radius r₁ and the radius r₂ is calculated from the NO_X storable amount which shows the amount of NO_X which can be stored.

FIG. 16 schematically shows the NO_X storable amount when performing SO_X release control in the sulfur poisoning recovery treatment. The timing t, is the timing when starting the SO_X release control, while the timing t, is the timing when ending the SO_X release control. In the present embodiment, the time when the SO_X storage amount becomes the residual SO_X storage amount is made the end timing t_e. The timing t₁ is any timing when performing the SO_X release control.

The NO_X storage reduction catalyst has an initial NO_X storable amount Q₀ at the timing t_s. By performing SO_X release control, the SO_X is released. The NO_X storable amount Q_t1 at the timing t₁ becomes larger than the initial NO_X storable amount Q₀. That is, the NO_X storable amount is restored. When performing the SO_X release control until the SO_X storage amount becomes the residual SO_X storage amount S_e, the NO_X storable amount becomes the final NO_X storable amount Q_e.

In the first release model in the present embodiment, in the same way as the first release model in Embodiment 2, a circle is defined centered about the catalyst metal 46. The area of the circle is deemed to correspond to the SO_X release amount (see FIG. 13). Furthermore, in the present embodiment, the SO_X release amount is replaced with the NO_X recovery amount to calculate the ratio of the radius r₁ and the radius r₂. The ratio of the radius r₁ and the radius r₂ becomes the following formula.

r ₂ /r ₁=(N_t1/N_e)^1/2  (20)

Here, the variable N_e is the recoverable NO_X storable amount (final NO_X recovery amount) which shows the recovery amount when performing SO_X release control from the timing t_s to when the SO_X storage amount becomes the residual SO_X storage amount S_e. The variable N_tt is the NO_X storable amount which is recovered from the timing t, to the timing t₁ and is called the “NO_X recovery amount”.

FIG. 17 shows a graph of the relationship between the final NO_X storable amount and the bed temperature of the NO_X storage reduction catalyst when performing SO_X release control. It is learned that as the temperature of the NO_X storage reduction catalyst becomes higher, the final NO_X storable amount Q_e becomes larger. As shown in FIG. 7, by the temperature of the NO_X storage reduction catalyst becoming higher, the residual SO_X storage amount S_e becomes smaller, so this trend appears.

In the present embodiment, the relationship shown in FIG. 17 is used as the basis to prepare in advance a map of the final NO_X storable amount Q_e as a function of the bed temperature of the NO_X storage reduction catalyst. This is stored in the electronic control unit 30. It is possible to detect the temperature of the NO_X storage reduction catalyst and use the map of the NO_X storable amount so as to detect the final NO_X storable amount Q_e.

Alternatively, the final NO_X storable amount Q_e can be calculated by subtracting from the total NO_X storable amount Q_total an amount corresponding to the residual SO_X storage amount S_e. The total NO_X storable amount Q_total is stored in advance in the electronic control unit 30. The residual SO_X storage amount S_e can for example be detected from a map of the residual SO_X storage amount as a function of temperature. The total NO_X storable amount Q_total and the residual SO_X storage amount S_e can be used to calculate the final NO_X storable amount Q_e.

By subtracting from the final NO_X storable amount Q_e the initial NO_X storable amount Q₀, it is possible to calculate the restorable NO_X storable amount N_e. The initial NO_X storable amount Q₀ can be calculated by subtracting from the final NO_X storable amount Q_e the initial SO_X storage amount S₀.

FIG. 18 shows a graph of the NO_X storable amount of the NO_X storage reduction catalyst with respect to the SO_X storage amount. It is learned that the greater the SO_X storage amount, the smaller the NO_X storable amount becomes. The relationship shown in FIG. 18 is used as the basis to prepare in advance a map of an NO_X storable amount as a function of the SO_X storage amount and store it in the electronic control unit 30. By calculating the SO_X storage amount S_t1 at any timing t₁, it is possible to detect the NO_X storable amount Q_t1 at the timing t₁. By subtracting from the NO_X storable amount Q_t1 at the timing t₁ the initial NO_X storable amount Q₀ when starting the SO_X release control, it is possible to calculate the NO_X recovery amount N_t1 at the timing t₁.

Alternatively, referring to FIG. 16 and FIG. 8, the NO_X recovery amount N_t1 corresponds to the cumulative SO_X release amount M_t1. From the cumulative SO_X release amount M_t1 up to the timing t₁, it is possible to calculate the NO_X recovery amount N_t1 up to the timing t₁. Alternatively, it is possible at step 115 of the flow chart shown in FIG. 15 to calculate the NO_X recovery amount which was restored during Δt from the SO_X release amount during Δt and cumulatively add this NO_X recovery amount to calculate the NO_X recovery amount N_t1 at the timing t₁.

By entering the calculated restorable NO_X storable amount N_e, and NO_X recovery amount N_t1 into formula (20), the ratio of the radius r₁ and the radius r₂ can be calculated. By entering the ratio of the radius r₁ and the radius r₂ into the formula (7), it is possible to calculate the SO_X release speed R_t1* after correction.

Next, the second release model in the present embodiment will be explained. In the second release model in the present embodiment, in the same way as the second release model in Embodiment 2, a sphere is defined centered about the catalyst metal 46. The volume of the sphere is deemed to correspond to the SO_X release amount. Furthermore, the SO_X release amount is replaced with the NO_X recovery amount to calculate the ratio of the radius r₁ and the radius r₂.

In the case of the second release model in the present embodiment, the following formula may be used to find the ratio of the radius r₁ and the radius r₂.

r ₂ /r ₁=(N_t1/N_e)^1/2  (21)

By entering the value calculated at formula (21) into the formula (7), it is possible to calculate the SO_X release speed R_t1* after correction.

In the present embodiment, it is possible to precisely calculate the SO_X release speed. By using the formula of the SO_X release speed after correction to calculate the SO_X release amount, it is possible to calculate a more accurate SO_X release amount. Alternatively, it is possible to precisely calculate the SO_X storage amount which is stored in the NO_X storage catalyst.

Further, the exhaust purification system of an internal combustion engine in the present embodiment can replace the SO_X amount which is stored in the NO_X storage reduction catalyst with the NO_X amount for management and control.

The rest of the configuration, action, and effects are similar to those of Embodiment 1 or 2, so the explanations will not be repeated here.

The above embodiments may be suitably combined. In the above figures, the same or corresponding parts are assigned the same reference notations. Note that the above embodiments are illustrations and do not limit the invention. Further, the embodiments include changes shown in the claims.

Claims

1. An exhaust purification system of an internal combustion engine which arranges in an engine exhaust passage an NOX catalyst device which stores NOX which is contained in exhaust gas when an air-fuel ratio of the inflowing exhaust gas is lean and which releases the stored NOX when the air-fuel ratio of the inflowing exhaust gas becomes a stoichiometric air-fuel ratio or rich and which uses SOX release control which raises a temperature of the NOX catalyst device to an SOX releasable temperature when an SOX amount which is stored in the NOX catalyst device exceeds a predetermined allowable amount and which makes the air-fuel ratio of the exhaust gas which flows into the NOX catalyst device a stoichiometric air-fuel ratio or rich so as to make the stored SOX be released, an exhaust purification system of an internal combustion engine characterized in thatthe NOX catalyst device has a residual SOX storage amount which is dependent on the temperature of the NOX catalyst device when performing SOX release control and finally remains even if performing SOX release control andthe system uses the residual SOX storage amount of the current SOX release control as the basis to calculate the SOX release speed at each timing in the current SOX release control.

2. An exhaust purification system of an internal combustion engine as set forth in claim 1, characterized in that in the current SOX release control, the system uses a difference between a SOX storage amount at each timing and said residual SOX storage amount as the basis to calculate the SOX release speed at each timing.

3. An exhaust purification system of an internal combustion engine as set forth in claim 1, characterized in that the system uses the SOX release speed which was calculated at each timing of the SOX release control as the basis to calculate a cumulative SOX release amount which is released from the start of SOX release control to the current timing andcorrects the calculated SOX release speed at the current timing based on a ratio of a first radius and a second radius where when a releasable SOX amount obtained by subtracting from an SOX storage amount when starting SOX release control said residual SOX storage amount is deemed to correspond to an area of a circle of the first radius, a radius of a circle of an area corresponding to said cumulative SOX release amount is calculated as the second radius.

4. An exhaust purification system of an internal combustion engine as set forth in claim 1, characterized in that the NOX catalyst device has a final NOX storable amount at which NOX can be stored when said residual SOX storage amount remains, andthe system uses the SOX release speed which was calculated at each timing of the SOX release control as the basis to calculate an NOX recovery amount which is restored from the start of SOX release control to the current timing andcorrects the calculated SOX release speed at the current timing based on a ratio of a first radius and a second radius where when a restorable NOX storable amount obtained by subtracting from said final NOX storable amount an NOX storable amount when starting SOX release control is deemed to correspond to an area of a circle of the first radius, a radius of a circle of an area corresponding to said NOX recovery amount is calculated as the second radius.

5. An exhaust purification system of an internal combustion engine as set forth in claim 1, characterized in that the system uses the SOX release speed which was calculated at each timing of the SOX release control as the basis to calculate a cumulative SOX release amount which is released from the start of SOX release control to the current timing andcorrects the calculated SOX release speed at the current timing based on a ratio of a first radius and a second radius where when a releasable SOX amount obtained by subtracting from an SOX storage amount when starting SOX release control said residual SOX storage amount is deemed to correspond to a volume of a sphere of the first radius, a radius of a sphere of a volume corresponding to said cumulative SOX release amount is calculated as the second radius.

6. An exhaust purification system of an internal combustion engine as set forth in claim 1, characterized in that the NOX catalyst device has a final NOX storable amount at which storage of NOX is possible when said residual SOX storage amount remains, andthe system uses the SOX release speed which was calculated at the each timing of SOX release control as the basis to calculate an NOX recovery amount which is restored from the start of SOX release control to the current timing andcorrects the calculated SOX release speed at the current timing based on a ratio of a first radius and a second radius where when a restorable NOX storable amount obtained by subtracting from said final NOX storable amount an NOX storable amount when starting SOX release control is deemed to correspond to a volume of a sphere of the first radius, a radius of a sphere of a volume corresponding to said NOX recovery amount is calculated as the second radius.