This application is based on and incorporates herein by reference Japanese Patent Application No. 2014-15934 filed on Jan. 30, 2014.
The present disclosure relates to a reducing agent supplying device for supplying a hydrocarbon compound (fuel) as a reducing agent used for NOx reduction.
Generally, NOx (Nitrogen Oxides) contained in exhaust gas of an internal combustion engine is purified in reaction of the NOx with a reducing agent in the presence of a reducing catalyst. For example, a Patent Literature (JP 2009-162173 A) discloses a purifying system that uses fuel (hydrocarbon compound) for combustion of an internal combustion engine as a reducing agent, and the system supplies the fuel into an exhaust passage at a position upstream of a reducing catalyst.
The inventors of the present disclosure have studied a purifying system in which fuel mixed with air is partially oxidized with oxygen in the air to reform the fuel, and the reformed fuel is supplied into an exhaust passage as the reducing agent. According to the configuration, a reducing performance of the reducing agent is improved, whereby an NOx purification rate can be increased.
However, various components different in molecular structure are mixed in a hydrocarbon-based fuel (for example, light oil) on the market, and a mixture ratio of those components is different for each of oil producing areas or sales areas. Therefore, property of fuel on the market is diverse, and when fuel is partially oxidized to be reformed, the reducing performance of the reformed fuel is significantly affected by the difference in the property of the fuel before being reformed.
It is an objective of the present disclosure to provide a reducing agent supplying device that suppresses a decrease in an NOx purification rate due to the fuel property.
In an aspect of the present disclosure, a reducing agent supplying device is for a fuel combustion system that includes a NOx purifying device with a reducing catalyst arranged in an exhaust passage to purify NOx contained in exhaust gas of an internal combustion engine. The reducing agent supplying device supplies a reducing agent into the exhaust passage at a position upstream of the reducing catalyst.
The reducing agent supplying device includes a reforming device, an obtaining section and a controller. The reforming device mixes fuel, which is a hydrocarbon compound, with air into a mixture and reforms the fuel by partially oxidizing the fuel with oxygen in the air. A reformed fuel is supplied into the exhaust passage as the reducing agent. The obtaining section obtains a physical quantity as a property index. The physical quantity has a correlation with property of the fuel that is supplied to the reforming device. The controller controls the reforming device according to the property index obtained by the obtaining section.
According to the aspect of the present disclosure, the physical quantity correlated with the property of fuel that is supplied to the reforming device is acquired as a property index, and the operation of the reforming device is controlled according to the acquired property index. For that reason, for example, when fuel has the property that the reducing performance of the fuel after being reformed is not sufficient, the reforming device is controlled to improve the reducing performance by increasing a supply amount of the reducing agent or improving the reforming action by the reforming device. Hence, a decrease in the NOx purification rate due to the fuel property can be suppressed.
The disclosure, together with additional objectives, features and advantages thereof, will be best understood from the following description, the appended claims and the accompanying drawings, in which:
A plurality of embodiments of the present disclosure will be described hereinafter referring to drawings. In the embodiments, a part that corresponds to a matter described in a preceding embodiment may be assigned with the same reference numeral, and redundant explanation for the part may be omitted. When only a part of a configuration is described in an embodiment, another preceding embodiment may be applied to the other parts of the configuration. The parts may be combined even if it is not explicitly described that the parts can be combined. The embodiments may be partially combined even if it is not explicitly described that the embodiments can be combined, provided there is no harm in the combination.
A combustion system as illustrated in
The supercharger 11 includes a turbine 11a, a rotating shaft 11b and a compressor 11c. The turbine 11a is disposed in an exhaust passage 10ex for the internal combustion engine 10 and rotates by kinetic energy of exhaust gas. The rotating shaft 11b connects an impeller of the turbine 11a to an impeller of the compressor 11c and transmits a rotating force of the turbine 11a to the compressor 11c. The compressor 11c is disposed in an intake passage 10in of the internal combustion engine 10 and supplies intake air to the internal combustion engine 10 after compressing (i.e., supercharging) the intake air.
A cooler 12 is disposed in the intake passage 10in downstream of the compressor 11c. The cooler 12 cools intake air compressed by the compressor 11c, and the compressed intake air cooled by the cooler 12 is distributed into plural combustion chambers of the internal combustion engine 10 through an intake manifold after a flow amount of the compressed intake air is adjusted by a throttle valve 13.
The regenerating DOC 14a (Diesel Oxidation Catalyst), the DPF 14 (Diesel Particulate Filter), the NOx purifying device 15, and the purifying DOC 16 are disposed in this order in the exhaust passage 10ex downstream of the turbine 11a. The DPF 14 collects particulates contained in exhaust gas. The regenerating DOC 14a includes a catalyst that oxidizes unburned fuel contained in the exhaust gas and that burns the unburned fuel. By burning the unburned fuel, the particulates collected by the DPF 14 are burned and the DPF 14 is regenerated, whereby the collecting capacity of the DPF 14 is maintained. It should be noted that this burning by the unburned fuel inside the regenerating DOC 14a is not constantly executed but is temporarily executed when the regeneration of the DPF 14 is required.
A supply passage 32 of the reducing agent supplying device is connected to the exhaust passage 10ex downstream of the DPF 14 and upstream of the NOx purifying device 15. A reformed fuel generated by the reducing agent supplying device is supplied as a reducing agent into the exhaust passage 10ex through the supply passage 32. The reformed fuel is generated by partially oxidizing hydrocarbon (i.e., fuel), which is used as a reducing agent, into partially oxidized hydrocarbon, such as aldehyde, as will be described later with reference to
The NOx purifying device 15 includes a honeycomb carrier 15b for carrying a reducing catalyst and a housing 15a housing the carrier 15b therein. The NOx purifying device 15 purifies NOx contained in exhaust gas through a reaction of NOx with the reformed fuel in the presence of the reducing catalyst, i.e., a reduction process of NOx into N2. It should be noted that, although O2 is also contained in the exhaust gas in addition to NOx, the reformed reducing agent selectively (preferentially) reacts with NOx in the presence of O2.
In the present embodiment, the reducing catalyst has adsorptivity to adsorb NOx. More specifically, the reducing catalyst demonstrates the adsorptivity to adsorb NOx in the exhaust gas when a catalyst temperature is lower than an activation temperature at which reducing reaction by the reducing catalyst can occur. Whereas, when the catalyst temperature is higher than the activation temperature, NOx adsorbed by the reducing catalyst is reduced by the reformed reducing agent and then is released from the reducing catalyst. For example, the NOx purifying device 15 may provide NOx adsorption performance with a silver/alumina catalyst that is carried by the carrier 15b.
The purifying DOC 16 has a housing that houses a carrier carrying an oxidation catalyst. The purifying DOC 16 oxidizes the reducing agent, which flows out from the NOx purifying device 15 without being used for NOx reduction, in the presence of the oxidation catalyst. Thus, the reducing agent can be prohibited from releasing into an atmosphere through an outlet of the exhaust passage 10ex. It should be noted that an activation temperature of the oxidation catalyst (e.g., 200° C.) is lower than the activation temperature (e.g., 250° C.) of the reducing catalyst.
Next, the reducing agent supplying device will be described below. Generally, the reducing agent supplying device generates the reformed fuel and supplies the reformed fuel into the exhaust passage 10ex through the supply passage 32. The reducing agent supplying device includes a reforming device A1 and an electric control unit (ECU 80), as will be described below. The reforming device A1 includes a discharging reactor 20 (ozone generator), an air pump 20p, a reaction container 30, a fuel injector 40 and a heater 50.
The discharging reactor 20 includes a housing 22 having a fluid passage 22a therein and a plurality of pairs of electrodes 21 are arranged inside the fluid passage 22a. More specifically, the electrodes 21 are held within the housing 22 through electric insulating members. The electrodes 21 have a plate shape and are arranged to face each other in parallel. One electrode 21, which is grounded, and the other electrode 21, which is applied with high voltage when electric power is supplied to the discharging reactor 20, are alternately arranged. Power application to the electrodes 21 is controlled by a microcomputer 81 of the ECU 80.
Air that is blown by the air pump 20p flows into the housing 22 of the discharging reactor 20. The air pump 20p is driven by an electric motor, and the electric motor is controlled by the microcomputer 81. The air blown by the air pump 20p flows into the fluid passage 22a within the housing 22, and flows through discharging passages 21a formed between the electrodes 21.
The reaction container 30 is attached to a downstream side of the discharging reactor 20, and a reaction chamber 30a is formed inside the reaction container 30. In the reaction chamber 30a, fuel is mixed with air into a mixture and the fuel is oxidized with oxygen in the air. Air that passed through the discharging passages 21a flows into the reaction chamber 30a through an air inlet 30c, and thereafter spouts from an injection port 30b formed in the reaction container 30. The injection port 30b is in communication with the supply passage 32.
The fuel injector 40 is attached to the reaction container 30. Fuel in liquid form (liquid fuel) within a fuel tank 40t is supplied to the fuel injector 40 by a pump 40p, and injected into the reaction chamber 30a through injection holes (not shown) of the fuel injector 40. The fuel within the fuel tank 40t is also used for combustion as described above, and thus the fuel is commonly used for combustion of the internal combustion engine 10 and used as the reducing agent. The fuel injector 40 has an injection valve and the valve is actuated by an electromagnetic force by an electromagnetic solenoid. The microcomputer 81 controls electric power supply to the electromagnetic solenoid.
The heater 50 is attached to the reaction container 30, and the heater 50 has a heating element (not shown) that generates heat when electric power is supplied to the heating element. The electric power supply to the heating element is controlled by the microcomputer 81. A heat generating surface of the heater 50 is positioned inside the reaction chamber 30a, and heats liquid fuel injected from the fuel injector 40. The liquid fuel heated by the heater 50 is vaporized within the reaction chamber 30a. The vaporized fuel is further heated to a given temperate or higher by the heater 50. As a result, the fuel is thermally decomposed into hydrocarbon that has a small carbon number, i.e., cracking occurs.
The fuel injector 40 is located above the heat generating surface of the heater 50, and the liquid fuel is injected from the fuel injector 40 onto the heat generating surface. The liquid fuel that adheres to the heat generating surface is vaporized.
A temperature sensor 31 that detects a temperature inside the reaction chamber 30a is attached to the reaction container 30. Specifically, the temperature sensor 31 is arranged above the heat generating surface of the heater 50 within the reaction chamber 30a. A temperature detected by the temperature sensor 31 is a temperature of the vaporized fuel after reacting with air. The temperature sensor 31 outputs information (detected temperature) on the detected temperature to the ECU 80.
When the electric power is supplied to the discharging reactor 20, electrons emitted from the electrodes 21 collide with oxygen molecules contained in air in the discharging passages 21a. As a result, ozone is generated from the oxygen molecules. That is, the discharging reactor 20 brings the oxygen molecules into a plasma state through a discharging process, and generates ozone as active oxygen. Then, the ozone generated by the discharging reactor 20 is contained in air that flows into the reaction chamber 30a.
A cool flame reaction is generated in the reaction chamber 30a. In the cool flame reaction, fuel in gas form is partially oxidized with oxygen or ozone within air. The fuel partially oxidized is called “reformed fuel”, and partial oxide (for example, aldehyde) may be one of examples of the reformed fuel in which a portion of the fuel (hydrocarbon compound) is oxidized with an aldehyde group (CHO).
It should be noted that fuel under a high temperature environment burns by self-ignition by oxidation reaction with oxygen contained in air, even in the atmospheric pressure. Such an oxidation reaction by the self-ignition combustion is also called “hot flame reaction” in which carbon dioxide and water are generated while generating heat. However, when a ratio (equivalent ratio) of the fuel and the air, and the ambient temperature fall within given ranges, a period for which an oxidation reaction stays in the cool flame reaction becomes longer as described below, and thereafter the hot flame reaction occurs. That is, the oxidation reaction occurs in two steps, the cool flame reaction and the hot flame reaction (refer to
The cool flame reaction is likely to occur when the ambient temperature is low, and the equivalent ratio is low. In the cool flame reaction, fuel is partially oxidized with oxygen contained in the ambient air. When the ambient temperature rises due to heat generation caused by the cool flame reaction, and thereafter a given time elapses, the fuel that is partially oxidized (for example, aldehyde) is oxidized, whereby the hot flame reaction occurs. When the partially oxidized fuel, such as aldehyde, generated through the cool flame reaction is used as an NOx purification reducing agent, an NOx purification rate is improved as compared with a case in which the fuel not partially oxidized is used.
As indicated by the symbol L1, when the heater temperature is 530° C., there is almost no period to stay in the cool flame reaction, and the oxidation reaction is completed with only one step. On the contrary, when the heater temperature is set to 330° C. or 430° C. as indicated by the symbols L2 and L3, the two-step oxidation reaction occurs. Also, when the heater temperature is set to 330° C., a start timing of the cool flame reaction is delayed as compared with a case where the heater temperature is set to 430° C., as indicated by the symbols L2 and L3. Also, when the heater temperature is set to 230° C. or lower, as indicated by the symbols L4 to L6, none of the cool flame reaction and the hot flame reaction occurs, i.e., the oxidation reaction does not occur.
In the simulation illustrated in
The following findings may be obtained from the results in
When the ambient temperature is adjusted to an optimal temperature (for example, 370° C.) within the given temperature range, the equivalent ratio that enables the two-step oxidation reaction becomes a maximum value (for example, 1.0). Therefore, in order to early generate the cool flame reaction, the heater temperature may be adjusted to the optimal temperature, and the equivalent ratio may be set to 1.0. However, since the cool flame reaction does not occur when the equivalent ratio exceeds 1.0, it is desirable to adjust the equivalent ratio to a value smaller than 1.0 by a margin. In the simulation illustrated in
The microcomputer 81 of the ECU 80 includes a memory unit to store programs, and a central processing unit executing an arithmetic processing according to the programs stored in the memory unit. The ECU 80 controls the operation of the internal combustion engine 10 based on detection values of sensors. The sensors may include an accelerator pedal sensor 91, an engine speed sensor 92, a throttle opening sensor 93, an intake air pressure sensor 94, an intake amount sensor 95, an exhaust temperature sensor 96, or the like.
The accelerator pedal sensor 91 detects a depressing amount of an accelerator pedal of a vehicle by a driver. The engine speed sensor 92 detects a rotational speed of an output shaft 10a of the internal combustion engine 10 (i.e., an engine rotational speed). The throttle opening sensor 93 detects an opening amount of the throttle valve 13. The intake air pressure sensor 94 detects a pressure of the intake passage 10in at a position downstream of the throttle valve 13. The intake amount sensor 95 detects a mass flow rate of intake air.
The ECU 80 generally controls an amount and injection timing of fuel for combustion that is injected from a fuel injection valve (not shown) according to a rotational speed of the output shaft 10a and an engine load of the internal combustion engine 10. Further, the ECU 80 controls the operation of the reforming device A1 based on an exhaust temperature detected by the exhaust temperature sensor 96. In other words, the microcomputer 81 switches between the generation of the reformed fuel and the generation of the ozone by repeatedly executing a process (i.e., a program) as shown in
At Step 10 of
More specifically, at Step 11, the air pump 20p is operated with a predetermined power amount. Next, at Step 12, it is determined whether the NOx catalyst temperature is lower than an activation temperature T1 of the reducing catalyst (e.g., 250° C.). The NOx catalyst temperature is estimated using an exhaust temperature detected by the exhaust temperature sensor 96. It should be noted that the activation temperature of the reducing catalyst is a temperature at which the reformed fuel can purify NOx through the reduction process.
When it is determined that the NOx catalyst temperature is lower than the activation temperature T1, a subroutine process for an ozone generation control is executed (Step 13). Initially, a predetermined power amount is supplied to the electrodes 21 of the discharging reactor 20 to start electrically discharging. Next, electric power supply to the heater 50 is stopped, and electric supply to the fuel injector 40 is stopped.
According to the ozone generation control, the discharging reactor 20 generates ozone and the generated ozone is supplied into the exhaust passage 10ex through the reaction chamber 30a and the supply passage 32. In this case, if power supply to the heater 50 is implemented, the ozone would be heated by the heater 50 and collapse. Also, if fuel is supplied, the ozone inside the discharging reactor 20 would react with the supplied fuel. In view of this, in the above-mentioned ozone generation control, heating by the heater 50 and the fuel supply are stopped. For that reason, since the reaction of the ozone with the fuel, and the heating collapse can be avoided, the generated ozone is supplied into the exhaust passage 10ex as it is.
When it is determined that the NOx catalyst temperature is equal to or higher than the activation temperature T1 in
An outline of the process in
Further, in Step 60, the power supply to the discharging reactor 20 is controlled according to a concentration of fuel within the reaction container 30. Accordingly, ozone is generated, and the generated ozone is supplied into the reaction container 30. Thus, the start timing of the cool flame reaction is advanced, and the cool flame reaction time is reduced. Hence, even when the reaction container 30 is downsized so that a staying time of fuel within the reaction container 30 is decreased, the cool flame reaction can be completed within the staying time, whereby the reaction container 30 can be downsized.
The microcomputer 81 executing Step 30 may provide “temperature controller (controller)”. The microcomputer 81 executing Step 40 may provide “fuel injection amount controller (controller)”. The microcomputer 81 executing Step 50 may provide “equivalent ratio controller (controller)”. The microcomputer 81 executing Step 60 may provide “discharging power controller (controller)”.
Hereinafter, the details of those steps S30, S40, S50, and S60 will be described with reference to
First, a description will be given of the process of Step 30 by the temperature controller. In Step 31, a temperature in the reducing agent supplying device, that is, a temperature within the reaction container 30 is obtained. Specifically, a detection temperature Tact detected by the temperature sensor 31 is obtained. In subsequent Step 32, an amount of heating by the heater 50 is adjusted so that the detection temperature Tact matches a target temperature Ttrg based on a difference ΔT between the target temperature Ttrg that is predetermined and the detection temperature Tact.
Specifically, a power supply duty ratio to the heater 50 is adjusted according to the difference ΔT. The target temperature Ttrg used in Step 32 is set to an ambient temperature (for example, 370° C.) at which the equivalent ratio becomes maximum in the above two-step oxidation reaction region. Since a temperature of the reaction chamber 30a rises during the cool flame reaction, a temperature of the heater 50 per se is controlled to be a value lower than the target temperature Ttrg by a temperature rising amount during the cool flame reaction.
Subsequently, a description will be given of the process of Step 40 by the fuel injection amount controller. In Step 41, a value for supplying fuel, which is necessary to reduce all of NOx that flows into the NOx purifying device 15, into the NOx purifying device 15 without excess or deficiency is set as a target fuel flow rate Ftrg. The target fuel flow rate Ftrg is the mass of the fuel to be supplied into the NOx purifying device 15 per unit time.
Specifically, the target fuel flow rate Ftrg is set based on an NOx inflow rate that will be described below, and the NOx catalyst temperature. The NOx inflow rate is the mass of NOx that flows into the NOx purifying device 15 per unit time. For example, the NOx inflow rate can be estimated based on an operating condition of the internal combustion engine 10. The NOx catalyst temperature is a temperature of the reducing catalyst inside the NOx purifying device 15. For example, the NOx catalyst temperature can be estimated based on a temperature detected by the exhaust temperature sensor 96.
The target fuel flow rate Ftrg increases as the NOx inflow rate increases. Also, since a reduced amount (reducing performance) of NOx in the presence of the reducing catalyst changes according to the NOx catalyst temperature, the target fuel flow rate Ftrg is set according to a difference in the reducing performance at the NOx catalyst temperature. For example, a map representing an optimum value of the target fuel flow rate Ftrg with respect to the NOx inflow rate and the NOx catalyst temperature is stored in the microcomputer 81 in advance. The target fuel flow rate Ftrg is set with reference to the map based on the NOx inflow rate and the NOx catalyst temperature.
In subsequent Step 42, the operation of the fuel injector 40 is controlled to inject fuel based on the target fuel flow rate Ftrg set at Step 41. Specifically, an opening time of the fuel injector 40 increases as the target fuel flow rate Ftrg increases, thereby increasing an injected fuel amount during one valve opening operation. The target fuel flow rate Ftrg may correspond to “target injection amount”.
Subsequently, a description will be given of the process of Step 50 by the equivalent ratio controller. In Step 51, a target equivalent ratio φtrg that provides the cool flame reaction corresponding to the detection temperature Tact is calculated. Specifically, a maximum value φmax of the equivalent ratio, which corresponds to the ambient temperature and which is the maximum value of the equivalent ratio in the two-step oxidation reaction region, is stored as the target equivalent ratio φtrg in the microcomputer 81 in advance. For example, a map of a value of the target equivalent ratio φtrg corresponding to the ambient temperature is prepared and the map is stored in advance. Then, the target equivalent ratio φtrg corresponding to the detection temperature Tact is calculated with reference to the map.
In subsequent Step 52, a target air flow rate Atrg is calculated based on the target equivalent ratio φtrg set at Step 51, and the target fuel flow rate Ftrg set at Step 42. Specifically, the target air flow rate Atrg is so calculated as to meet φtrg=Ftrg/Atrg. In subsequent Step 53, the operation of the air pump 20p is controlled based on the target air flow rate Atrg calculated at Step 52. Specifically, the energization duty ratio to the air pump 20p increases as the target air flow rate Atrg increases.
Then, a description will be given of the process of Step 60 by the discharging power controller. Initially, a target ozone flow rate Otrg is calculated at Step 61 based on the target fuel flow rate Ftrg set at Step 41. Specifically, the target ozone flow rate Otrg is calculated so that a ratio of an ozone concentration to a fuel concentration inside the reaction chamber 30a becomes a given value (for example, 0.2). For example, the ratio is set so that the cool flame reaction can be completed within a given time (for example, 0.02 sec).
In subsequent Step 62, a target energization amount Ptrg to the discharging reactor 20 is calculated based on the target air flow rate Atrg calculated at Step 52 and the target ozone flow rate Otrg calculated at Step S61. That is, an energizing power to the discharging reactor 20 is controlled according to the target energization amount Ptrg to adjust a generation amount of ozone to a target generation amount.
Specifically, since the staying time of air in the discharging passages 21a decreases as the target air flow rate Atrg increases, the target energization amount Ptrg is controlled to be increased. Also, the target energization amount Ptrg increases as the target ozone flow rate Otrg increases. In subsequent Step 63, the energization amount to the discharging reactor 20 is controlled based on the target energization amount Ptrg calculated at Step 62. Specifically, the energization duty ratio to the discharging reactor 20 increases as the target energization amount Ptrg increases.
According to the process described above in
The axis of abscissa in
Moreover, as illustrated in
That is, in Step 70 of
In more detail, an NOx sensor 97 is disposed in the exhaust passage 10ex downstream of the NOx purifying device 15 and the NOx sensor 97 detects an NOx outflow amount that has not been reduced by the NOx purifying device 15. Further, an NOx inflow amount, which is exhausted from the internal combustion engine 10 and flows into the NOx purifying device 15, is estimated based on the operating condition of the internal combustion engine 10. Then, a rate of the NOx outflow amount to the NOx inflow amount is calculated as the NOx purification rate.
In subsequent Step 71, it is determined whether the property index (NOx purification rate) obtained at Step 70 falls within a normal range. For example, when the NOx purification rate is less than a preset lower limit value, occurring of abnormality in the NOx purifying device 15 or the reforming device A1 is estimated. Then, in Step 75, an abnormality flag is set to on, and a fact that the abnormality occurs is notified the user of.
On the other hand, when the property index obtained in Step 70 falls within the normal range, the control parameter of the reforming device A1 is changed according to property index in subsequent Step 72. For example, as illustrated in
That is, as illustrated in
In Step S73 of
When it is determined at Step 74 that the NOx purification rate (property index) is not improved for a given time or longer although the control parameter is corrected at Step 72, the process proceeds to the above-mentioned Step 75, and the abnormality flag is set to on.
The microcomputer 81 executing Step 70 may provide “obtaining section” that obtains the property index. The microcomputer 81 executing Step 72 may provide “property index controller (controller)” that controls the operation of the reforming device A1 according to the property index. The microcomputer 81 executing Step 71 may provide “abnormality determiner” that determines abnormality in the reforming device A1 or the NOx purifying device 15 when the property index has a value beyond a predetermined normal range.
As described above, the reducing agent supplying device according to the present embodiment obtains the NOx purification rate as the property index, and changes the control for the reforming device A1, that is, a fuel injection amount from the fuel injector 40 is changed according to the acquired NOx purification rate.
Specifically, when the fuel which has the low property index and not suitable for the reduction is supplied, the target fuel flow rate Ftrg (control parameter) is corrected to increase. For that reason, a reducing agent amount supplied into the exhaust passage 10ex increases, whereby a decrease in the NOx purification rate due to the fuel property can be suppressed. On the other hand, when the property index is high, the target fuel flow rate Ftrg is corrected to decrease. Hence, an excessive supply of a reducing agent amount into the exhaust passage 10ex is prevented. Accordingly, excessive or deficient supply of the reducing agent due to a difference in the fuel property can be suppressed.
Further, in the present embodiment, the target fuel flow rate Ftrg in the plural control parameters for the reforming device A1 is changed according to the property index. For that reason, since the supply amount of the reducing agent is controlled according to the difference in the fuel property, it can be realized with high precision to provide the supply amount of the reducing agent that corresponds to the fuel property.
Further, in the present embodiment, the NOx purification rate is obtained as the property index, and assuming that the reducing performance of the generated reformed fuel decreases as the NOx purification rate decreases, the operation of the reforming device A1 is controlled so that the NOx purification rate by the NOx purifying device 15 increases. Since the correlation between the NOx purification rate and the fuel property is high, the difference in the fuel property can be reflected on the control of the reforming device A1 with high precision and with a high response.
Further, in the present embodiment, when the NOx purification rate as the property index has a value beyond the normal range at Step 71 of
Further in the present embodiment, the reforming device A1 includes the reaction container 30 in which fuel is oxidized with oxygen in air. A temperature within the reaction container 30 and the equivalent ratio are adjusted to generate the cool flame reaction, and fuel (reformed fuel) partially oxidized through the cool flame reaction is supplied into the exhaust passage 10ex as the NOx purification reducing agent. For that reason, the NOx purification rate can be improved as compared with a case in which fuel not partially oxidized is used as the reducing agent.
Further, in the present embodiment, the discharging reactor 20 is provided, and ozone generated by the discharging reactor 20 is supplied into the reaction container 30 when the cool flame reaction is generated. For that reason, the start timing of the cool flame reaction can be advanced, and the cool flame reaction time can be reduced. Hence, even when the reaction container 30 is downsized so that a staying time of the fuel within the reaction container 30 is reduced, the cool flame reaction can be completed within the staying time. Thus, the reaction container 30 can be downsized.
Further in the present embodiment, the electric power used for the electric discharge is controlled according to the concentration of fuel in the reaction chamber 30a through the process of Step 60 in
Further in the present embodiment, when a temperature of the reducing catalyst is lower than the activation temperature T1, ozone generated by the discharging reactor 20 is supplied into the reaction chamber 30a while stopping the fuel injection by the fuel injector 40, thereby supplying ozone into the exhaust passage 10ex. Accordingly, the reformed fuel as the reducing agent can be prevented from being supplied when the reducing catalyst in the NOx purifying device 15 is not activated. Since NO in the exhaust gas is oxidized into NO2 by supplying ozone, and is adsorbed inside the NOx purification catalyst, an NOx adsorption amount inside the NOx purifying device 15 can increase.
Further in the present embodiment, the heater 50 that heats the fuel, and the temperature sensor 31 that detects a temperature (ambient temperature) inside the reaction chamber 30a are provided. The temperature controller at Step 30 of
It should be noted that the equivalent ratio range where the cool flame reaction occurs may be different depending on a temperature inside the reaction chamber 30a. In the present embodiment taking the above fact into consideration, the equivalent ratio controller in Step 50 of
Further, in the present embodiment, the target fuel flow rate Ftrg is set at Step 40 (fuel injection amount controller) of
In the above-described embodiment, the target fuel flow rate Ftrg (control parameter) is corrected according to the fuel property so that the reducing agent amount to be supplied into the exhaust passage 10ex changes according to the fuel property. On the contrary, in the second embodiment, the target temperature Ttrg (control parameter) of the heater 50 is corrected according to the fuel property so that a temperature inside the reaction chamber 30a changes according to the fuel property.
That is, as illustrated in
In the first and second embodiments, the target fuel flow rate Ftrg or the target temperature Ttrg is corrected according to the fuel property. On the contrary, according to the third embodiment, the target energization amount Ptrg (control parameter) of the discharging reactor 20 is corrected according to the fuel property to change the supply amount of ozone into the reaction chamber 30a according to the fuel property.
That is, as illustrated in
In the first embodiment, the NOx purification rate is obtained as the property index. On the contrary, according to the fourth embodiment, a heat generating amount in the combustion chambers of the internal combustion engine 10 is obtained as the property index. Specifically, a heat generating amount in one combustion cycle is estimated based on a pressure within the combustion chambers which is detected by a cylinder pressure sensor, and a variation of a detected value of the engine speed sensor 92. As illustrated in
Accordingly, even in the present embodiment, a decrease in the NOx purification rate due to the fuel property can be suppressed. Also, in the present embodiment, since a heat generating amount is obtained as the property index, the property index can be obtained even when a temperature of the reducing catalyst is lower than the activation temperature T1, and the NOx purifying device 15 does not purify NOx.
Further in the present embodiment, the temperature sensor 31 that detects a temperature inside the reaction chamber 30a is provided, and the operation of the reforming device changes assuming that a heat generating amount during an oxidization reaction (reaction heat generating amount) decreases as the detection temperature by the temperature sensor 31 decreases. Specifically, the control parameter is changed such that the NOx purification rate increases. According to the above configuration, since a temperature inside the reaction chamber 30a is directly detected, the property index corresponding to a heat generating amount can be obtained with high precision.
In the first and fourth embodiments, the NOx purification rate or the heat generating amount is obtained as the property index. On the contrary, according to the fifth embodiment, an ignition delay time in the combustion chambers of the internal combustion engine 10 is obtained as the property index. Specifically, a time (ignition delay time) from fuel injection into the combustion chambers until self-ignition is calculated based on a pressure change within the combustion chambers, which is detected by the cylinder pressure sensor. As illustrated in
Accordingly, even in the present embodiment, a decrease in the NOx purification rate due to the fuel property can be suppressed. Also, in the present embodiment, since the ignition delay time is obtained as the property index, the property index can be obtained even when a temperature of the reducing catalyst is lower than the activation temperature T1, and the NOx purifying device 15 does not purify NOx.
In the fifth embodiment, the ignition delay time is obtained as the property index. On the contrary, in the present embodiment, a temperature in the reaction chamber 30a (reaction chamber temperature), that is, the detection temperature by the temperature sensor 31 is obtained as the property index. The reaction chamber temperature decreases as the reaction heat generating amount when the fuel is oxidized decreases. Under the circumstances, as illustrated in
Accordingly, even in the present embodiment, a decrease in the NOx purification rate due to the fuel property can be suppressed. Also, in the present embodiment, the reaction chamber temperature is obtained as the property index, and the reaction chamber temperature has a high correlation with the fuel property. Therefore, the property index with high precision can be obtained.
In the first embodiment illustrated in
Specifically, a branch pipe 36h connects between a portion of the intake passage 10in downstream of the compressor 11c and upstream of the cooler 12, and the fluid passage 22a of the discharging reactor 20. Also, a branch pipe 36c connects between a portion of the intake passage 10in downstream of the cooler 12 and the fluid passage 22a. A high temperature intake air without being cooled by the cooler 12 is supplied into the discharging reactor 20 through the branch pipe 36h. Whereas, a low temperature intake air after being cooled by the cooler 12 is supplied into the discharging reactor 20 through the branch pipe 36c.
An electromagnetic valve 36 that opens and closes an internal passage of the respective branch pipes 36h and 36c is attached to the branch pipes 36h and 36c. The operation of the electromagnetic valve 36 is controlled by the microcomputer 81. When the electromagnetic valve 36 operates to open the branch pipe 36h and close the branch pipe 36c, the high temperature intake air flows into the discharging reactor 20. When the electromagnetic valve 36 operates to open the branch pipe 36c and close the branch pipe 36h, the low temperature intake air flows into the discharging reactor 20.
The operation of the electromagnetic valve 36 allows switching between a mode in which the high temperature intake air without being cooled by the cooler 12 branches off from an upstream of the cooler 12, and a mode in which the low temperature intake air after being cooled by the cooler 12 branches off from a downstream of the cooler 12. In this case, the mode for supplying the low temperature intake air is selected during the ozone generation control, and the generated ozone is prohibited from being destroyed by heat of the intake air. The mode for supplying the high temperature intake air is selected during other than the ozone generation control, and fuel heated by the heater 50 is prohibited from being cooled by the intake air within the reaction chamber 30a. Also, the opening of the electromagnetic valve 36 is controlled, thereby controlling an amount of portions of the intake air that is compressed by the supercharger 11 and is to be supplied into the discharging reactor 20.
During a period for which the electromagnetic valve 36 is opened, an amount of intake air that flows into the combustion chambers of the internal combustion engine 10 is reduced by an amount of portions of the intake air that flow through the branch pipes 36h and 36c. For that reason, the microcomputer 81 corrects the opening of the throttle valve 13 or a compressing amount by the compressor 11c so that an amount of intake air flowing into the combustion chambers increases by the amount of the intake air flowing through the branch pipes 36h and 36c during the opening period of the electromagnetic valve 36.
As described above, a reforming device A2 according to the present embodiment includes the electromagnetic valve 36, and the electromagnetic valve 36 is opened to supply a portion of the intake air compressed by the supercharger 11 into the discharging reactor 20. For that reason, air containing oxygen can be supplied into the discharging reactor 20 without the air pump 20p as illustrated in
The reforming device A1 illustrated in
In the reforming device A1 illustrated in
The preferred embodiments of the present invention have been described above. However, the present invention is not limited to the embodiments described above, but can be implemented with various modifications as exemplified below.
In the above-described embodiments, any one of the control parameters of the target temperature Ttrg, the target fuel flow rate Ftrg, the target air flow rate Atrg, and the target energization amount Ptrg is changed according to the property index. On the contrary, the plural control parameters may be changed according to the property index.
In the embodiment illustrated in
In the above-described embodiment as shown in
In the above-described embodiment illustrated in
When the reducing agent supplying device is in a complete stop state in which generation of both the ozone and the reformed reducing agent is stopped, the electric discharge at the discharging reactor 20 may be stopped to reduce wasteful electric consumption. The reducing agent supplying device may be in the complete stop state when, for example, the NOx catalyst temperature is lower than the activation temperature and the NOx adsorbed amount reaches the saturation amount, or when the NOx catalyst temperature becomes high beyond a max temperature at which the reducing catalyst can reduce NOx. Further, the operation of the air pump 20p may be stopped in the complete stop state so as to reduce wasteful power consumption.
In the above-described embodiment as shown in
The NOx purifying device 15 may adsorb NOx when an air-fuel ratio in the internal combustion engine 10 is leaner than a stoichiometric air-fuel ratio (i.e., when the engine 10 is in lean combustion) and may reduce NOx when the air-fuel ratio in the internal combustion engine 10 is not leaner than the stoichiometric air-fuel ratio (i.e., when the engine 10 is in non-lean combustion). In this case, ozone is generated at the lean combustion and the reformed reducing agent is generated at the non-lean combustion. One of examples of a catalyst that adsorbs NOx at the lean combustion may be a chemisorption reducing catalyst made of platinum and barium carried by a carrier.
The reducing agent supplying device may be applied to a combustion system that has the NOx purifying device 15 without adsorption function (i.e., physisorption and chemisorption functions). In this case, in the NOx purifying device 15, an iron-based or copper-based catalyst may be used as the catalyst having the NOx reducing performance in a given temperature range in the lean combustion, and a reforming substance may be supplied to those catalysts as the reducing agent.
In the above-described embodiment, the NOx catalyst temperature used at Step 12 of
In the above-described embodiment as shown in
In the above-described embodiment as shown in
Means and functions provided by the ECU may be provided by, for example, only software, only hardware, or a combination thereof. The ECU may be constituted by, for example, an analog circuit.
Number | Date | Country | Kind |
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2014-15934 | Jan 2014 | JP | national |
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7093429 | Cho | Aug 2006 | B1 |
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2000-54833 | Feb 2000 | JP |
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Entry |
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English translation of Japanese Patent Application Publication No. JP 201-149388 A (Aug. 4, 2011). |
Office Action (3 pages) dated Mar. 1, 2016, issued in corresponding Japanese Application No. 2014-015934 and English translation (3 pages). |
2004 “Diesel Exhaust Emission Control II—Nox After Treatment Technology”, JSAE Annual Congress, Society of Automotive Engineers of Japan, Inc., May 20, 2004, 12 pages. |
Number | Date | Country | |
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20150211402 A1 | Jul 2015 | US |