The present invention relates to an exhaust purification device of an internal combustion engine.
In the past, there have been known SOx concentration sensors arranged inside engine exhaust gas passages so as to detect the SOx concentration in the exhaust gas. These known SOx concentration sensors normally use solid electrolytes and measure the electromotive force generated by the change of SOx into sulfate ion to detect the SOx concentration in the exhaust gas (for example, see Japanese Patent Publication (A) No. 2004-239706).
However, a conventional SOx detection system using this kind of SOx concentration sensor can only operate under high temperatures and becomes bulky as an apparatus. In particular, when the SOx concentration is low, there is the large problem of not being able to detect the SOx concentration. Conventionally, as in this SOx concentration sensor, attention has only been directed at instantaneously and directly detecting the SOx concentration in the exhaust gas. So long as trying to instantaneously and directly detect the SOx concentration in the exhaust gas in such a way, various problems inevitably occur like as explained above.
Therefore, the inventors changed their way of thinking and focused not on instantaneously detecting the SOx concentration, but on detecting the cumulative amount of sulfur S over a long period. It has been proven that by changing the way of thinking in this way, it would be possible to easily estimate the amount of SOx in the exhaust gas even without directly detecting the SOx concentration in the exhaust gas.
An object of the present invention is to provide an exhaust purification device of an internal combustion engine capable of easily detecting the amount of SOx flowing into a catalyst.
According to the present invention, there is provided an exhaust purification device of an internal combustion engine arranging an exhaust gas purification catalyst inside an engine exhaust gas passage, wherein a sample gas for sulfur detection is generated from fuel of a smaller amount than an amount of fuel fed to a combustion chamber and proportional to the amount of fuel fed to the combustion chamber, an SOx sensor having a sensor part trapping a sulfur contained inside the sample gas and capable of detecting an amount of sulfur trapped at the sensor part from changes in property of the sensor part is provided, and an amount of SOx flowing into the catalyst is detected from an output value of the SOx sensor.
Referring to
The fuel tank 6 has a fuel feed pump 9 attached to it. The fuel discharged from the fuel feed pump 9 is divided at a fuel divider 10 into injection fuel and sample fuel. The injection fuel is fed through a fuel feed pipe 11 to a common rail 12 for distributing fuel to the fuel injectors 3, while the sample fuel is fed through a fuel feed pipe 13 to a sample gas generation chamber 14 formed around the exhaust pipe 7. The sample fuel fed into this sample gas generation chamber 14 is a much smaller amount than the amount of injection fuel fed to the combustion chamber 2 and proportional to the amount of injection fuel fed to the combustion chamber 2.
As shown in
An electronic control unit 20 is comprised of a digital computer provided with a ROM (read only memory) 22, RAM (random access memory) 23, CPU (microprocessor) 24, input port 25, and output port 26 all connected to each other by a bidirectional bus 21. The output of the SOx sensor 16 is calibrated at a detection circuit 29, while the calibrated output is input through a corresponding AD converter 27 to the input port 25. Further, an accelerator pedal 30 is connected to a load sensor 31 generating an output voltage proportional to the depression amount L of the accelerator pedal 30. The output voltage of the load sensor 31 is input through a corresponding AD converter 27 to the input port 25. Further, the input port 25 has a crank angle sensor 32 generating an output pulse every time the crank shaft rotates by for example 15° connected to it. On the other hand, the output port 26 are connected to the fuel injectors 3, fuel feed pump 9, and air pump 15 through corresponding drive circuits 28.
Next, the method of detection of the sulfur component will be explained for the case where barium Ba which is one of an alkali earth metal, or a compound of the same is used as the metal or metal compound 40.
Barium Ba becomes barium oxide BaO in the atmosphere. This barium oxide BaO, when placed in the exhaust gas, immediately changes to barium carbonate BaCO3 due to the CO and CO2 contained in the exhaust gas. Further, this barium carbonate BaCO3 changes to barium nitrate Ba(NO3)2 due to the NOx in the exhaust gas.
That is, when barium Ba is used, the metal or metal compound 40 shown in
On the other hand, the fuel contains sulfur. Accordingly, the sample gas contains sulfur. This sulfur S is trapped in the metal or metal compound 40 and changes to a sulfur-containing metal compound 41 shown in
Note that if the air-fuel ratio of the sample gas is lean, that is, the sample gas contains a sufficient amount of oxygen, and the temperature of the sample gas is higher than 300° C. or so, the sulfur in the sample gas becomes easier to trap in the form of SOx in the metal or metal compound 40, that is, in the sensor part of the SOx sensor 16. Accordingly, in the embodiment shown in
On the other hand,
If the oxide changes to sulfate or if the metal oxide changes to a sulfide, its properties change. Accordingly, the amount of sulfur trapped can be detected from the change in these properties. On the other hand, as mentioned above, the amount of fuel fed in the sample gas generation chamber 14 is proportional to the amount of fuel injection fed into the combustion chamber 2. Accordingly, if the amount of sulfur in the sample gas is known, the amount of sulfur in the exhaust gas, that is, the amount of SOx flowing into the catalyst 8, can be determined.
Therefore, in the present invention, an SOx sensor 16 having a sensor part trapping the sulfur contained in the sample gas and capable of detecting the amount of sulfur trapped in the sensor part from a change in property of the sensor part is provided and the amount of SOx flowing into the catalyst 8 is detected from the output value of the SOx sensor 16.
Next, referring to
The electric resistance R of the sensor part for detection 51 becomes higher if the ambient temperature becomes higher. Accordingly, the sensor part for reference 53 is provided to remove the effect that this kind of temperature change has on the electric resistance. For example, a detection circuit 29 (
As shown in
In this example, the heat capacity of the metal compound 64 is estimated from the response of the change in the resistance of the thermistor element 61 when the temperature around the sensor part for detection 65 changes, the heat capacity of the metal compound 63 is estimated from the response of the change in the resistance of the sensor part for reference 67 when the temperature around the thermistor element 63 changes, and the trapped amount of sulfur S is found from the difference of these heat capacities.
That is, specifically, a Wheatstone bridge such as shown in
In the example shown in
Further, if making the sensor part for detection 65 a high temperature, the trapped SOx is released from the metal compound 64 and the sensor part for detection 65 is regenerated. Accordingly, in this example, by operating the heater 69, the temperature of the sensor part for detection 65 rises, thereby allowing the regeneration of the sensor part for detection 65. Note that, in this case, even if the air-fuel ratio of the sample gas becomes temporarily rich, the sensor part for detection 65 can be regenerated.
In the embodiment shown in
Referring to
Number | Date | Country | Kind |
---|---|---|---|
2007-128954 | May 2007 | JP | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
---|---|---|---|---|
PCT/JP2008/059300 | 5/14/2008 | WO | 00 | 1/29/2009 |
Publishing Document | Publishing Date | Country | Kind |
---|---|---|---|
WO2008/143273 | 11/27/2008 | WO | A |
Number | Name | Date | Kind |
---|---|---|---|
7267991 | Ceccarini et al. | Sep 2007 | B2 |
20030134425 | Ceccarini et al. | Jul 2003 | A1 |
20070065341 | Asanuma | Mar 2007 | A1 |
20090308053 | Nishioka et al. | Dec 2009 | A1 |
Number | Date | Country |
---|---|---|
A-60-198433 | Oct 1985 | JP |
A-2000-230419 | Aug 2000 | JP |
A-2002-058958 | Feb 2002 | JP |
A-2004-239706 | Aug 2004 | JP |
Number | Date | Country | |
---|---|---|---|
20090320450 A1 | Dec 2009 | US |