WO2009060290A2 - Exhaust purifying device of internal combustion engine - Google Patents

Exhaust purifying device of internal combustion engine Download PDF

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Publication number
WO2009060290A2
WO2009060290A2 PCT/IB2008/002964 IB2008002964W WO2009060290A2 WO 2009060290 A2 WO2009060290 A2 WO 2009060290A2 IB 2008002964 W IB2008002964 W IB 2008002964W WO 2009060290 A2 WO2009060290 A2 WO 2009060290A2
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WO
WIPO (PCT)
Prior art keywords
catalyst
nox
lower layer
noble
upper layer
Prior art date
Application number
PCT/IB2008/002964
Other languages
French (fr)
Other versions
WO2009060290A3 (en
Inventor
Kenji Sakurai
Shigeki Miyashita
Kenji Katoh
Naoto Miyoshi
Hiroto Imai
Original Assignee
Toyota Jidosha Kabushiki Kaisha
Cataler Corporation
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
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Publication date
Application filed by Toyota Jidosha Kabushiki Kaisha, Cataler Corporation filed Critical Toyota Jidosha Kabushiki Kaisha
Priority to DE112008002983.0T priority Critical patent/DE112008002983B4/en
Priority to US12/741,841 priority patent/US20110079001A1/en
Publication of WO2009060290A2 publication Critical patent/WO2009060290A2/en
Publication of WO2009060290A3 publication Critical patent/WO2009060290A3/en

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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/92Chemical or biological purification of waste gases of engine exhaust gases
    • B01D53/94Chemical or biological purification of waste gases of engine exhaust gases by catalytic processes
    • B01D53/9404Removing only nitrogen compounds
    • B01D53/9409Nitrogen oxides
    • B01D53/9413Processes characterised by a specific catalyst
    • B01D53/9422Processes characterised by a specific catalyst for removing nitrogen oxides by NOx storage or reduction by cyclic switching between lean and rich exhaust gases (LNT, NSC, NSR)
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/92Chemical or biological purification of waste gases of engine exhaust gases
    • B01D53/94Chemical or biological purification of waste gases of engine exhaust gases by catalytic processes
    • B01D53/9445Simultaneously removing carbon monoxide, hydrocarbons or nitrogen oxides making use of three-way catalysts [TWC] or four-way-catalysts [FWC]
    • B01D53/945Simultaneously removing carbon monoxide, hydrocarbons or nitrogen oxides making use of three-way catalysts [TWC] or four-way-catalysts [FWC] characterised by a specific catalyst
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/92Chemical or biological purification of waste gases of engine exhaust gases
    • B01D53/94Chemical or biological purification of waste gases of engine exhaust gases by catalytic processes
    • B01D53/9459Removing one or more of nitrogen oxides, carbon monoxide, or hydrocarbons by multiple successive catalytic functions; systems with more than one different function, e.g. zone coated catalysts
    • B01D53/9477Removing one or more of nitrogen oxides, carbon monoxide, or hydrocarbons by multiple successive catalytic functions; systems with more than one different function, e.g. zone coated catalysts with catalysts positioned on separate bricks, e.g. exhaust systems
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F01MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
    • F01NGAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
    • F01N13/00Exhaust or silencing apparatus characterised by constructional features ; Exhaust or silencing apparatus, or parts thereof, having pertinent characteristics not provided for in, or of interest apart from, groups F01N1/00 - F01N5/00, F01N9/00, F01N11/00
    • F01N13/009Exhaust or silencing apparatus characterised by constructional features ; Exhaust or silencing apparatus, or parts thereof, having pertinent characteristics not provided for in, or of interest apart from, groups F01N1/00 - F01N5/00, F01N9/00, F01N11/00 having two or more separate purifying devices arranged in series
    • F01N13/0097Exhaust or silencing apparatus characterised by constructional features ; Exhaust or silencing apparatus, or parts thereof, having pertinent characteristics not provided for in, or of interest apart from, groups F01N1/00 - F01N5/00, F01N9/00, F01N11/00 having two or more separate purifying devices arranged in series the purifying devices are arranged in a single housing
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F01MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
    • F01NGAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
    • F01N3/00Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust
    • F01N3/08Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous
    • F01N3/0807Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous by using absorbents or adsorbents
    • F01N3/0814Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous by using absorbents or adsorbents combined with catalytic converters, e.g. NOx absorption/storage reduction catalysts
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F01MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
    • F01NGAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
    • F01N3/00Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust
    • F01N3/08Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous
    • F01N3/0807Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous by using absorbents or adsorbents
    • F01N3/0828Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous by using absorbents or adsorbents characterised by the absorbed or adsorbed substances
    • F01N3/0842Nitrogen oxides
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F01MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
    • F01NGAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
    • F01N3/00Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust
    • F01N3/08Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous
    • F01N3/10Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous by thermal or catalytic conversion of noxious components of exhaust
    • F01N3/101Three-way catalysts
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2255/00Catalysts
    • B01D2255/10Noble metals or compounds thereof
    • B01D2255/102Platinum group metals
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2255/00Catalysts
    • B01D2255/10Noble metals or compounds thereof
    • B01D2255/102Platinum group metals
    • B01D2255/1021Platinum
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2255/00Catalysts
    • B01D2255/20Metals or compounds thereof
    • B01D2255/202Alkali metals
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2255/00Catalysts
    • B01D2255/20Metals or compounds thereof
    • B01D2255/204Alkaline earth metals
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2255/00Catalysts
    • B01D2255/20Metals or compounds thereof
    • B01D2255/204Alkaline earth metals
    • B01D2255/2042Barium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2255/00Catalysts
    • B01D2255/90Physical characteristics of catalysts
    • B01D2255/902Multilayered catalyst
    • B01D2255/9022Two layers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2255/00Catalysts
    • B01D2255/90Physical characteristics of catalysts
    • B01D2255/91NOx-storage component incorporated in the catalyst
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/40Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
    • B01J23/46Ruthenium, rhodium, osmium or iridium
    • B01J23/464Rhodium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/54Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/56Platinum group metals
    • B01J23/63Platinum group metals with rare earths or actinides
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J37/00Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/02Impregnation, coating or precipitation
    • B01J37/0234Impregnation and coating simultaneously
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J37/00Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/02Impregnation, coating or precipitation
    • B01J37/024Multiple impregnation or coating
    • B01J37/0244Coatings comprising several layers
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F01MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
    • F01NGAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
    • F01N2370/00Selection of materials for exhaust purification
    • F01N2370/02Selection of materials for exhaust purification used in catalytic reactors
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F01MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
    • F01NGAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
    • F01N2510/00Surface coverings
    • F01N2510/06Surface coverings for exhaust purification, e.g. catalytic reaction
    • F01N2510/068Surface coverings for exhaust purification, e.g. catalytic reaction characterised by the distribution of the catalytic coatings
    • F01N2510/0682Surface coverings for exhaust purification, e.g. catalytic reaction characterised by the distribution of the catalytic coatings having a discontinuous, uneven or partially overlapping coating of catalytic material, e.g. higher amount of material upstream than downstream or vice versa
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F01MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
    • F01NGAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
    • F01N2530/00Selection of materials for tubes, chambers or housings
    • F01N2530/26Multi-layered walls
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02TCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
    • Y02T10/00Road transport of goods or passengers
    • Y02T10/10Internal combustion engine [ICE] based vehicles
    • Y02T10/12Improving ICE efficiencies

Definitions

  • the invention relates to an exhaust purifying device of an internal conit ⁇ istion engine.
  • a NOx storage-reduction catalyst which adsorbs NOx contained in exhaust gas flowing into the catalyst when the air-fuel ratio of the exhaust gas is lean, and releases and reduces the adsorbed NOx when the air-fuel ratio of the exhaust gas becomes rich, is disposed in an exhaust passage of the engine (i.e., lean-burn engine ) in which an air-fuel mixture having a lean air-fuel ratio is normally burned.
  • the air-fuel ratio of the exhaust gas flowing into the NOx storage-reduction catalyst is temporarily switched to the rich side when the NOx stored in the NOx storage-reduction catalyst is to be released and reduced.
  • NOx contained in the exhaust gas is adsorbed by and stored in the NOx storage-reduction catalyst.
  • the amount of NOx stored in the NOx storage -reduction catalyst gradually increases with the passage of time.
  • the air-fuel ratio of the exhaust gas flowing into the NOx storage -reduction catalyst is temporarily switched to the rich side before the NOx storage -reduction catalyst is saturated with NOx, so that the NOx stored in the NOx storage -reduction catalyst is released and reduced.
  • the air-fuel ratio in the internal combustion engine is controlled to be rich (i.e., smaller than the stoichiometric ratio) so that the air-fuel ratio of the exhaust gas flowing into the NOx storage-reduction catalyst is switched to the rich side.
  • an upstream catalyst and a downstream catalyst are arranged in series with each other and are housed in a common casing disposed in an engine exhaust passage, and each of the upstream catalyst and the downstream catalyst has a single-layer structure or a multi-layer structure.
  • the NOx storage-reduction catalyst Since fuel consumption increases with an increase in the frequency at which the air-fuel ratio of the exhaust gas flowing into the NOx storage -reduction catalyst is switched to the rich side, it is preferable, in terms of reduction of the fuel consumption, that the NOx storage-reduction catalyst has the highest possible NOx adsorbing capability or storage capacity.
  • the space in which the NOx storage-reduction catalyst is installed there is a limit to the space in which the NOx storage-reduction catalyst is installed, and it is therefore necessary to increase or enhance the NOx adsorbing capability of the NOx storage-reduction catalyst while minimizing the dimensions or capacity of the NOx storage -reduction catalyst.
  • an additional catalyst may be disposed upstream or downstream of the NOx storage -reduction catalyst, or the NOx storage-reduction catalyst may have a multi-layer structure, i.e., may be constructed of two or more layers, as disclosed in JP-A-2006-291812.
  • the state of the art does not provide satisfactory solutions to the above problems.
  • the invention provides an exhaust purifying device of an internal combustion engine in which a NOx storage-reduction catalyst exhibits a high NOx adsorbing capability and a high NOx conversion efficiency.
  • an exhaust purifying device of an internal combustion engine wherein an upstream catalyst and a downstream catalyst are arranged in series with each other and are housed in a common casing disposed in an engine exhaust passage, and wherein the upstream catalyst comprises a NOx storage-reduction catalyst that adsorbs NOx contained in incoming exhaust gas when the air-fuel ratio of the incoming exhaust gas is lean, and releases and reduces the adsorbed NOx when the air-fuel ratio of the incoming exhaust gas becomes rich, and the downstream catalyst comprises one of a three-way catalyst and a NOx storage-reduction catalyst.
  • the upstream catalyst and the downstream catalyst are prepared such that the upstream catalyst has a higher oxidizing capability than the downstream catalyst, and such that the downstream catalyst has a higher reducing capability than the upstream catalyst, and the upstream catalyst has a multi-layer structure including an upper layer and a lower layer, and is prepared such that the upper layer has a higher oxidizing capability than the lower layer, and such that the lower layer has a higher reducing capability than the upper la ⁇ ⁇ er.
  • each of the upper layer and the lower layer of the upstream catalyst may contain a noble-metal catalyst comprising at least one selected from platinum (Pt), palladium (Pd), osmium (Os), gold (Au), rhodium (Rh), iridium (Ir), and ruthenium (Ru), and a NOx absorbent comprising at least one selected from alkali metals, alkaline earths, and rare earths.
  • a noble-metal catalyst comprising at least one selected from platinum (Pt), palladium (Pd), osmium (Os), gold (Au), rhodium (Rh), iridium (Ir), and ruthenium (Ru)
  • a NOx absorbent comprising at least one selected from alkali metals, alkaline earths, and rare earths.
  • the upper layer of the upstream catalyst may contain, as the noble-metal catalyst, at least one selected from platinum (Pt), palladium (Pd), osmium (Os), and gold (Au), and the lower layer of the upstream catalyst may contain, as the noble-metal catalyst, at least one selected from rhodium (Rh), iridium (Ir), and ruthenium (Ru).
  • the downstream catalyst may have a multi-layer structure including an upper layer and a lower layer, and may be prepared such that the upper layer has a higher reducing capability than the lower layer, and the lower layer has a higher oxidizing capability than the upper layer.
  • rhodium (Rh) may be used as a noble -metal component of the upper layer of the downstream catalyst
  • platinum (Pt ) may be used as a noble-metal component of the lower layer of the downstream catalyst.
  • the downstream catalyst may have a single-layer structure.
  • the downstream catalyst may contain rhodium (Rh) and platinum (Pt) as noble-metal components.
  • the air-fuel ratio in the internal combustion engine rna ⁇ r be normally set to a lean air-fuel ratio that is larger than a stoichiometric ratio, and, when NOx stored in the NOx storage -reduction catalyst is to be released and reduced, the air-fuel ratio of exhaust gas flowing into the NOx storage-reduction catalyst may be temporarily controlled to a rich air-fuel ratio that is smaller than the stoichiometric ratio.
  • the air-fuel ratio in the internal combustion engine may be temporarily controlled to the stoichiometric ratio, depending on engine operating conditions.
  • FIG. 1 is an overall view of an internal combustion engine ;
  • FIG. 2 is a cross-sectional view of a NOx storage-reduction catalyst;
  • FIG. 3A and FIG. 3B are cross- sectional views of a surface portion of a catalyst support;
  • FIG. 4 is an enlarged cross-sectional view of the NOx storage -reduction catalyst;
  • FIG. 5A through FIG. 5 C are views showing various examples of NOx storage -reduction catalysts
  • FIG. 6A and FIG. 6B are views showing various examples of three-way catalysts
  • FIG. 7 is a view useful for explaining a predetermined load factor KLX
  • FIG. 8 is a flowchart illustrating an engine operation control routine
  • FIG. 9A through FIG. 9C are view showing various experimental results.
  • FIG. 10 is a view useful for explaining a peak value of a discharged NOx amount.
  • FIG. 1 illustrates the case where the invention is applied to a spark ignition type internal combustion engine.
  • the invention may also be applied to a compression ignition type internal combustion engine.
  • the spark ignition type internal combustion engine includes an engine body 1, cylinder block 2, cylinder head 3, piston 4, combustion chamber 5, intake valve 6, intake port 7, exhaust valve 8, exhaust port 9, and a spark plug 10.
  • the intake port 7 of each cylinder is connected to a surge tank 12 via a corresponding intake branch pipe 11.
  • the surge tank 12 is connected to an air cleaner 14 via an intake duct 13.
  • An air flow meter 15 and a throttle valve 17 adapted to be driven by a step motor 16 are disposed in the intake duct 13.
  • a fuel injection valve 18 is mounted to the intake port 7 of each cylinder.
  • the fuel injection valve 18 for each cylinder is connected to a common rail 19, and the common rail 19 is connected to a fuel tank 21 via a fuel pump 20 capable of controlling the amount of fuel delivered therefrom.
  • a fuel pressure sensor 22 is mounted to the common rail 19, and the amount of fuel delivered from the fuel pump 20 is controlled so that the fuel pressure in the common rail 19 becomes equal to a target pressure.
  • each cylinder is connected to a casing 25 via an exhaust manifold 23 and an exhaust pipe 24, and the casing 25 is connected to an exhaust pipe 26.
  • An air-fuel ratio sensor 27 is mounted in the exhaust pipe 24, and a catalyst 28 is housed in the casing 25.
  • An electronic control unit 30 consists of a digital computer, and includes ROM (read-only memory ) 32, RAM (random access memory) 33, CPU (microprocessor ) 33, input port 35, and output port 36, which are connected to each other via a bidirectional bus 31.
  • a load sensor 40 that produces an output voltage proportional to the amount of depression of an accelerator pedal 39 is connected to the accelerator pedal 39.
  • the input port 35 receives output voltages of the air flow meter 15, fuel pressure sensor 22, air-fuel ratio sensor 27 and the load sensor 40, via corresponding A/D converters 37.
  • a crank angle sensor 41 produces an output pulse each time the crankshaft rotates, for example, 30°, and the output pulse is transmitted to the input port 35.
  • the CPU 34 calculates the engine speed Ne, based on the output pulses received from the crank angle sensor 41.
  • the output port 36 is connected to the spark plug 10, step motor 16, fuel injection valve 18, and the fuel pump 20, via corresponding driving circuits 38.
  • the catalyst 28 includes an upstream catalyst 28U and a downstream catalyst 28D which are arranged in series with each other in the casing 25.
  • the upstream catalyst 28U consists of a NOx storage-reduction catalyst
  • the downstream catalyst 28D consists of a three-way catalyst.
  • the downstream catalyst 28D may consist of a NOx storage -reduction catalyst.
  • the capacity of the upstream catalyst 28U is made equal to or larger than that of the downstream catalyst 28D.
  • the capacity of the upstream catalyst 28U may be made smaller than that of the downstream catalyst 28D.
  • FIG. 2 illustrates the structure of the upstream catalyst, or NOx storage -reduction catalyst 28U.
  • the NOx storage -reduction catalyst 28U has a honeycomb structure, and includes a plurality of exhaust gas channels 51 that are separated from each other by thin partition walls 50.
  • a catalyst support 55 made of, for example, alumina is loaded on the opposite surfaces of each partition wall, or substrate 50.
  • FIG. 3A and FIG. 3B schematically illustrate a cross-section of a surface portion of the catalyst support 55. As shown in FIG. 3A and FIG.
  • a noble-metal catalyst 56 is supported, while being scattered, on the surface of the catalyst support 55, and a layer of a NOx absorbent 57 is formed on the surface of the catalyst support 55.
  • alkali metals such as potassium (Iv), sodium (Na), and cesium (Cs )
  • alkaline earths such as barium (Ba) and calcium (Ca )
  • rare earths such as lanthanum (La) and yttrium (Y).
  • the NOx absorbent 57 performs NOx absorbing and releasing functions to absorb NOx when the air-fuel ratio of exhaust gas is lean, and release the absorbed NOx when the concentration of oxygen in the exhaust gas is reduced.
  • barium (Ba) is used as a component that constitutes the NOx absorbent 57, by waj' of example, when the air-fuel ratio of exhaust gas is lean, namely, when the concentration of oxygen in the exhaust gas is high, NOx contained in the exhaust gas is oxidized into NO2 on the platinum (Pt) 56 as shown in FIG. 3A, and NO2 is then absorbed into the NOx absorbent 57, to be dispersed in the form of nitrate ions NO3 ' in the NOx absorbent 57 while combining with barium carbonate (BaCOa ) . In this manner, NOx is absorbed into the NOx absorbent 57.
  • NO2 is produced on the surface of the platinum (Pt) 56 as long as the concentration of oxygen in the exhaust gas is sufficiently high, and NO 2 is absorbed into the NOx absorbent 57 to form nitrate ions NO3 ' as long as the NOx absorbing capability of the NOx absorbent 57 is not saturated.
  • the concentration of oxygen in the exhaust gas is reduced, and the reaction proceeds in the reverse direction (NO3 ' -» NO 2), so that nitrate ions NO3 ' in the NOx absorbent 57 are released in the form of NO2 from the NOx absorbent 57, as shown in FIG. 3B. Then, the released NOx is reduced by unburned HC and CO contained in the exhaust gas.
  • the NOx storage-reduction catalyst 28U has a multi-layer structure including an upper layer 28UU and a lower layer 28UL, as shown in FIG. 4. Namely, the lower layer 28UL and the upper layer 28UU are successively laminated on the substrate 50.
  • each of the upper layer 28UU and the lower layer 28LHL provides a NOx storage -reduction catalyst, namely, includes the above "described noble-metal catalyst 56 and NOx absorbent 57.
  • An additional layer may be provided between the upper layer 28L T U and the lower layer 2SL 7 L, or between the lower layer 28L 1 L and the catalyst support 55.
  • At least one selected from noble metals having a high oxidizing capability such as platinum (Pt ) , palladium (Pd), osmium (Os ) , and gold (Au) is used as the noble-metal catalyst 56 of the upper layer 28XJU.
  • at least one selected from noble metals having a high reducing capability such as rhodium (Rh), iridium (Ir), and ruthenium (Ru), is used as the noble-metal catalyst 56 of the lower layer 28L T L.
  • a noble metal having a high reducing capability is not contained in the upper layer 28UU.
  • FIG. 5A through FIG. 5C show various examples of the noble-metal catalysts 58 of the upper layer 28ULi and the lower layer 28L T L.
  • the noble-metal catalyst 56 of the upper layer 28UU platinum (Pt) is used in the example of FIG. 5A, and palladium (Pd) is used in the example of FIG. 5B, while platinum (Pt) and palladium (Pd) are used in the example of FIG. 5C.
  • rhodium (Rh) is used as the noble-metal catalyst 56 of the lower layer 28UL in all of the examples of FIG. 5A- FIG. 5C.
  • the noble-metal catalysts 56 of the upper layer 28UU and lower layer 29UL are selected in the above manners, the oxidizing capability of the upper layer 28UU is made higher than that of the lower layer 28L 7 L, and the reducing capability of the lower lasher 28UL is made higher than that of the upper layer 28UU.
  • the downstream catalyst, or three-way catalyst are selected in the above manners, the oxidizing capability of the upper layer 28UU is made higher than that of the lower layer 28L 7 L, and the reducing capability of the lower lasher 28UL is made higher than that of the upper layer 28UU.
  • the 28D also has a honeycomb structure, like the NOx storage-reduction catalyst 28LT, and includes a plurality of exhaust gas channels that are separated from each other by thin partition walls.
  • a catalyst support made of, for example, alumina is loaded on the opposite surfaces of each partition wall, and a catalyst component including a noble-metal component is supported on the surface of the catalyst support.
  • the three-way catalyst 28D has a multi-layer structure including an upper layer 28DU and a lower layer 28DL.
  • each of the upper layer 28DU and the lower layer 28DL provides a three-way catalyst.
  • At least one selected from noble metals having a high reducing capability is used as a noble-metal component of the upper layer 2SDU, and at least one selected from noble metals having a high oxidizing capability is used as a noble-metal component of the lower layer 28DL.
  • rhodium (Rh) is used as the noble-metal component of the upper layer 28DU
  • platinum (Pt) is used as the noble-metal component of the lower layer 28DL.
  • the reducing capability of the upper layer 28DU is made higher than that of the lower layer 28DL, and the oxidizing capability of the lower layer 28DL is made higher than that of the upper layer 28DU.
  • the three-way catalyst 28D may have a single -layer structure.
  • at least a noble metal having a high reducing capability is used as a noble-metal component of the three-way catalyst 28D.
  • a metal having a high oxidizing capability may be used or may not be used.
  • rhodium (Rh) and platinum (Pt ) are used as noble-metal components of the three-way catalyst 28D.
  • the noble-metal catalysts 56 of the upstream catalyst or NOx storage-reduction catalyst 28LT and the noble-metal component(s ) of the downstream catalyst or three-way catalyst 28D are selected as described above, the oxidizing capability of the NOx storage -reduction catalyst 28U is made higher than that of the three-way catalyst 28D, and the reducing capability of the three-way catalyst 28D is made higher than that of the NOx storage-reduction catalyst 28LT.
  • the upstream catalyst or NOx storage-reduction catalyst 28U and the downstream catalyst or three-way catalyst 28D are independently supported on the respective substrates, and these substrates are coupled in series with each other, thereby to form the catalyst 28.
  • the NOx storage-reduction catalyst 28U may be supported on an upstream portion of a common substrate, and the three-way catalyst 28D may be supported on a downstream portion of the substrate.
  • the NOx storage-reduction catalyst 28U having a multi-layer structure is manufactured, for example, in the following manner.
  • the manufacturing method will be explained with regard to the case where rhodium (Rh) is used as the noble-metal catalyst 56 of the lower layer 28UL, and platinum (Pt) is used as the noble-metal catalyst 56 of the upper layer 28LTU.
  • rhodium (Rh) is used as the noble-metal catalyst 56 of the lower layer 28UL
  • platinum (Pt) is used as the noble-metal catalyst 56 of the upper layer 28LTU.
  • a slurry is prepared in which support powder that forms the catalyst support of the lower layer 28LTL and rhodium powder are dispersed, and the slurry is applied onto a substrate.
  • zirconium (Zr), alumina (AI2O3), ceria (CeO 2 ), ZrOa-Al 2 Os, ZrO 2 -AIiOs-TiOa may be used as the catalyst support of the lower layer 28UL.
  • the rhodium powder is formed from PM powder, and is dispersed in the form of nitrate or acetate in the slurry.
  • the viscosity of the slurry is preferably around 30%, for example, and the amount of coating preferably ranges from 50g/L to 200g/L. Then, drying (200 0 C, 2 hours) and firing (400 0 C, 4 hours ) are conducted, so that the lower layer 28UL is formed.
  • a slurry is prepared in which support powder that forms the catalyst support of the upper layer 28UU and platinum powder are dispersed, and the slurry is applied onto the lower layer 28UL.
  • zirconium (Zr), alumina (AI2O3 ) , ceria (CeOo), AIaOs-CeOa, ZrOa-Al 2 Os, or ZrOa-Al 2 Os-TiO 2 for example, may be used as the catalyst support of the upper layer 28ULT.
  • the platinum powder is dispersed in the form of nitrate or acetate, such as tetrachi'oloplatinum or dinitroplatinum, in the sluriy.
  • the viscosity of the slurry is preferably around 30%, for example, and the amount of coating preferably ranges from 50g/L to 200g/L. Then, drying (200°C, 2 hours ) and firing (400 0 C, 4 hours) are conducted, so that the upper layer 28LTU is formed.
  • a catalyst support may be first formed on the lower layer 28LTL. and the catalyst support may be impregnated with an aqueous solution of tetrachroloplatinum or dinitroplatinum.
  • the three-way catalyst 28D having a multi-layer structure may also be manufactured in a manner similar to the NOx storage-reduction catalyst 28U.
  • a lean-mode operation is performed in which an air-fuel mixture having a lean air-fuel ratio is burned.
  • a stoichiometric-ratio operation is performed in which an air-fuel mixture having the stoichiometric ratio is burned.
  • the engine load factor IvL represents the proportion of the engine load to the full load.
  • the airfuel ratio of exhaust gas flowing into the NOx storage-reduction catalyst 28U becomes lean, and NOx contained in the exhaust gas is adsorbed by and stored in the NOx storage-reduction catalyst 28U. If the lean-mode operation continues to be performed, however, the NOx storage-reduction catalyst 28U adsorbs NOx to the full NOx adsorbing capability (namely, the NOx storage-reduction catalyst 28U is saturated with NOx adsorbed thereon ) , whereby the NOx storage-reduction catalyst 28U becomes unable to adsorb NOx any more.
  • the air-fuel ratio of the exhaust gas is temporarily made rich before the NOx storage-reduction catalyst 28U reaches the full NOx adsorbing capability (i.e.. before the NOx storage reduction catalyst 28U is saturated with NOx), so that NOx is released from the NOx storage-reduction catalyst 28U, and reduced by HC, CO in the exhaust gas, into N2, or the like.
  • the amount of NOx adsorbed per unit time by the NOx storage-reduction catalyst 28U is stored in advance in the ROM 32, in the form of a map as a function of engine operating conditions, such as the engine load factor KL and the engine speed Ne.
  • a total value SN of the amount of NOx stored in the NOx storage-reduction catalyst 28U is calculated.
  • a rich-mode operation is temporarily performed in which an air-fuel mixture having a rich air-fuel ratio is burned.
  • NOx is released from the NOx storage-reduction catalyst 28U, and is reduced.
  • FIG. 8 illustrates a routine for implementing engine operation control according to the embodiment of the invention. This routine is executed as an interrupt at predetermined time intervals.
  • step 100 it is initially determined in step 100 whether the engine load factor KL is larger than the predetermined load factor KLX (FIG. 7). If KL ⁇ KLX, the control proceeds to step 101 in which a lean-mode operation is performed. In the following step 102, the total value SN of the stored NOx amount is calculated. In the following step 103, it is determined whether the total value SN of the stored NOx amount is larger than the upper limit MAX. If SN ⁇ MAX, the current cycle of the routine of FIG. 8 ends, and the lean-mode operation is continued. If SN > MAX, on the other hand, the control proceeds to step 104, and a rich-mode operation is performed, for example, for a given period of time.
  • step 105 the total value SN of the stored NOx amount is cleared. If it is determined in step 100 that the engine load factor KL is larger than the predetermined load factor KLX, the control proceeds to step 106 in which a stoichiometric-ratio operation is performed.
  • the NOx adsorbing capability of the catalyst 28 or the NOx storage-reduction catalyst 28U can be enhanced.
  • FIG. 9A shows experimental results on the NOx storage capacity ST of the catalyst 28.
  • the catalyst 28 consists solely of a NOx storage -reduction catalyst having a single-layer structure, and platinum (Pt) and rhodium (Rh) are used as a noble-metal catalyst.
  • the catalyst 28 consists solely of a NOx storage-reduction catalyst having a double-layer structure, and platinum (Pt) is used as a noble-metal catalyst of the upper layer while rhodium (Rh) is used as a noble-metal catalyst of the lower layer.
  • the catalyst 28 consists solely of a NOx storage-reduction catalyst having a double-layer structure, and platinum (Pt) and palladium (Pd) are used as a noble-metal catalyst of the upper layer while rhodium (Rh) is used as a noble-metal catalyst of the lower layer.
  • the NOx storage capacity ST of the catalyst 28 is relatively large in Examples EaI, Ea2, and is larger in Example Ea2 than in Example EaI. This may be because the NOx storage-reduction catalyst has a multi-layer structure, namely, consists of two laj ⁇ ers.
  • the frequency at which the air-fuel ratio of exhaust gas flowing into the catalyst 28 is switched to the rich side (on which the air-fuel ratio is smaller than the stoichiometric ratio) can be reduced, and fuel consumption (i.e., the amount of fuel consumed) can be reduced.
  • NOx discharged from the catalyst 28 per unit time rapidly increases, reaches its peak value PIvN, and then decreases.
  • the peak value PKN of the discharged NOx amount EXN can be reduced.
  • FIG. 9B shows experimental results on the peak value PKN of the discharged NOx amount of the catalyst 28.
  • the catalyst 28 consists solely of a NOx storage-reduction catalyst having a single-layer structure, and platinum (Pt) and rhodium (Rh) are used as a noble-metal catalyst.
  • the catalyst 28 consists solely of a NOx storage -reduction catalyst having a double-layer structure, and platinum (Pt) is used as a noble-metal component of the upper layer while rhodium
  • the catalyst 28 consists of an upstream catalyst and a downstream catalyst.
  • the upstream catalyst consists of a NOx storage-reduction catalyst having a double-layer structure, and platinum (Pt) is used as a noble-metal catalyst of the upper layer while rhodium (Rh) is used as a noble-metal catalyst of the lower layer.
  • the downstream catalyst consists of a three-way catalyst having a single-layer structure, and platinum (Pt) and rhodium (Rh) are used as noble-metal components.
  • the peak value PKN of the discharged NOx amount is larger in Comparative Example Cb2 than that of Comparative Example CbI.
  • the peak value PKN of the discharged NOx amount can be significantly reduced. This may be because NOx released from the upstream catalyst or NOx storage-reduction catalyst is reduced by the downstream catalyst. Accordingly, the NOx conversion efficiency can be held at a high level during lean-mode operation while assuring a large NOx storage capacity.
  • the NOx conversion efficiency EFFS of the catalyst 28 can be held at a high level when the air-fuel ratio of exhaust gas flowing into the catalyst 28 is substantially equal to the stoichiometric ratio, for example, during high-load operation.
  • FIG. 9C shows experimental results on the NOx conversion efficiency EFFS of the catalyst 28 when the air-fuel ratio of the incoming exhaust gas is substantially equal to the stoichiometric ratio.
  • the catalyst 28 consists solely of a NOx storage -reduction catalyst having a single-layer structure, and platinum (Pt) and rhodium (Rh) are used as a noble-metal catalyst.
  • the catalyst 28 consists solely of a three-way catafyst having a double-layer structure, and rhodium (Rh ) is used as a noble-metal catalyst of the upper layer while platinum (Pt) is used as a noble-metal catalyst of the lower layer.
  • the catalyst 28 consists of an upstream catalyst and a downstream catalyst.
  • the upstream catalyst consists of a NOx storage-reduction catalyst having a double-layer structure, and platinum (Pt) is used as a noble-metal catalyst of the upper layer while rhodium (Rh) is used as a noble-metal catalyst of the lower layer.
  • the downstream catalyst consists of a three-way catalyst having a single-layer structure, and platinum (Pt) and rhodium (Rh) are used as noble-metal components.
  • INN represents the amount of NOx flowing into the catalyst 28 per unit time
  • EXN represents the amount of NOx flowing out of the catalyst 28
  • the NOx conversion efficiency EFFS of the catalyst 28 may be expressed by the following equation:
  • the NOx conversion efficiency EFFS of Example Ec is higher than that of Comparative Example CcI, and is substantially equal to that of Comparative Example of Cc2.
  • a rich-mode operation i.e., operating the engine at a rich air-fuel ratio
  • the aii-fuel ratio of the incoming exhaust gas may be made rich by injecting fuel into the combustion chamber during the expansion stroke or exhaust stroke. It is also possible to make the air-fuel ratio of the incoming exhaust gas rich by supplying a reductant or secondary fuel into an exhaust passage upstream of the NOx storage-reduction catalyst 28U.
  • a lean-mode operation is performed when the engine operates at a low load
  • a stoichiometrkrratio operation is performed when the engine operates at a high load.
  • a stoichiometricratio operation may also be performed during acceleration.

Abstract

An upstream catalyst (28U) and a downstream catalyst (28D) are arranged in series and are housed in a common casing (25) disposed in an engine exhaust passage. The upstream catalyst (28U) consists of a NOx storage -reduction catalyst that adsorbs NOx contained in incoming exhaust gas when the air-fuel ratio of the incoming exhaust gas is lean, and releases and reduces the adsorbed NOx when the air-fuel ratio of the incoming exhaust gas becomes rich, and the downstream catalyst consists of a three-way catalyst. The upstream catalyst has a higher oxidizing capability than the downstream catalyst, and the downstream catalyst has a higher reducing capability than the upstream catalyst. The upstream catalyst has a multi-layer structure including an upper layer and a lower layer, and is prepared such that the upper layer has a higher oxidizing capability than the lower layer, and the lower layer has a higher reducing capability than the upper layer.

Description

EXHAUST PURIFYING DEVICE OF INTERNAL COMBUSTION ENGINE
BACKGROUND OF THE INVENTION
1. Field of the Invention [0001] The invention relates to an exhaust purifying device of an internal conitαistion engine.
2. Description of the Related Art
[0002] In a known example of internal combustion engine (as disclosed in. for example, Japanese Patent Application Publication No. 11-44234 (JP-A- 11-44234)), a NOx storage-reduction catalyst, which adsorbs NOx contained in exhaust gas flowing into the catalyst when the air-fuel ratio of the exhaust gas is lean, and releases and reduces the adsorbed NOx when the air-fuel ratio of the exhaust gas becomes rich, is disposed in an exhaust passage of the engine (i.e., lean-burn engine) in which an air-fuel mixture having a lean air-fuel ratio is normally burned. In this type of engine, the air-fuel ratio of the exhaust gas flowing into the NOx storage-reduction catalyst is temporarily switched to the rich side when the NOx stored in the NOx storage-reduction catalyst is to be released and reduced. In this internal combustion engine, NOx contained in the exhaust gas is adsorbed by and stored in the NOx storage-reduction catalyst. The amount of NOx stored in the NOx storage -reduction catalyst gradually increases with the passage of time. Thus, the air-fuel ratio of the exhaust gas flowing into the NOx storage -reduction catalyst is temporarily switched to the rich side before the NOx storage -reduction catalyst is saturated with NOx, so that the NOx stored in the NOx storage -reduction catalyst is released and reduced. In this case, the air-fuel ratio in the internal combustion engine, for example, is controlled to be rich (i.e., smaller than the stoichiometric ratio) so that the air-fuel ratio of the exhaust gas flowing into the NOx storage-reduction catalyst is switched to the rich side.
[0003] In another known example of internal combustion engine (as disclosed in, for example, Japanese Patent Application Publication No. 2006-291812 (JP-A-2006-291812)), an upstream catalyst and a downstream catalyst are arranged in series with each other and are housed in a common casing disposed in an engine exhaust passage, and each of the upstream catalyst and the downstream catalyst has a single-layer structure or a multi-layer structure.
[0004] Since fuel consumption increases with an increase in the frequency at which the air-fuel ratio of the exhaust gas flowing into the NOx storage -reduction catalyst is switched to the rich side, it is preferable, in terms of reduction of the fuel consumption, that the NOx storage-reduction catalyst has the highest possible NOx adsorbing capability or storage capacity. However, there is a limit to the space in which the NOx storage-reduction catalyst is installed, and it is therefore necessary to increase or enhance the NOx adsorbing capability of the NOx storage-reduction catalyst while minimizing the dimensions or capacity of the NOx storage -reduction catalyst. [0005] Immediately after the air-fuel ratio of the exhaust gas flowing into the NOx storage -reduction catalyst is switched to the rich side, a large amount of NOx may be discharged from the NOx storage-reduction catalyst without being reduced. In this case, emissions of NOx need to be reduced.
[0006] To solve the above-described problems, an additional catalyst may be disposed upstream or downstream of the NOx storage -reduction catalyst, or the NOx storage-reduction catalyst may have a multi-layer structure, i.e., may be constructed of two or more layers, as disclosed in JP-A-2006-291812. However, the state of the art does not provide satisfactory solutions to the above problems.
SUMMARY OF THE INVENTION
[0007] The invention provides an exhaust purifying device of an internal combustion engine in which a NOx storage-reduction catalyst exhibits a high NOx adsorbing capability and a high NOx conversion efficiency.
[0008] According to one aspect of the invention, there is provided an exhaust purifying device of an internal combustion engine wherein an upstream catalyst and a downstream catalyst are arranged in series with each other and are housed in a common casing disposed in an engine exhaust passage, and wherein the upstream catalyst comprises a NOx storage-reduction catalyst that adsorbs NOx contained in incoming exhaust gas when the air-fuel ratio of the incoming exhaust gas is lean, and releases and reduces the adsorbed NOx when the air-fuel ratio of the incoming exhaust gas becomes rich, and the downstream catalyst comprises one of a three-way catalyst and a NOx storage-reduction catalyst. In the exhaust purifying device, the upstream catalyst and the downstream catalyst are prepared such that the upstream catalyst has a higher oxidizing capability than the downstream catalyst, and such that the downstream catalyst has a higher reducing capability than the upstream catalyst, and the upstream catalyst has a multi-layer structure including an upper layer and a lower layer, and is prepared such that the upper layer has a higher oxidizing capability than the lower layer, and such that the lower layer has a higher reducing capability than the upper la}^er.
[0009] In the exhaust purifying device as described above, each of the upper layer and the lower layer of the upstream catalyst may contain a noble-metal catalyst comprising at least one selected from platinum (Pt), palladium (Pd), osmium (Os), gold (Au), rhodium (Rh), iridium (Ir), and ruthenium (Ru), and a NOx absorbent comprising at least one selected from alkali metals, alkaline earths, and rare earths.
[OOIO] In the exhaust purifying device as described above, the upper layer of the upstream catalyst may contain, as the noble-metal catalyst, at least one selected from platinum (Pt), palladium (Pd), osmium (Os), and gold (Au), and the lower layer of the upstream catalyst may contain, as the noble-metal catalyst, at least one selected from rhodium (Rh), iridium (Ir), and ruthenium (Ru).
[OOll] Also, the downstream catalyst may have a multi-layer structure including an upper layer and a lower layer, and may be prepared such that the upper layer has a higher reducing capability than the lower layer, and the lower layer has a higher oxidizing capability than the upper layer.
[0012] Furthermore, rhodium (Rh) may be used as a noble -metal component of the upper layer of the downstream catalyst, and platinum (Pt) may be used as a noble-metal component of the lower layer of the downstream catalyst. [0013] The downstream catalyst may have a single-layer structure. [0014] Furthermore, the downstream catalyst may contain rhodium (Rh) and platinum (Pt) as noble-metal components.
[0015] In the exhaust purifying device as described above, the air-fuel ratio in the internal combustion engine rna}r be normally set to a lean air-fuel ratio that is larger than a stoichiometric ratio, and, when NOx stored in the NOx storage -reduction catalyst is to be released and reduced, the air-fuel ratio of exhaust gas flowing into the NOx storage-reduction catalyst may be temporarily controlled to a rich air-fuel ratio that is smaller than the stoichiometric ratio. [0016] Furthermore, the air-fuel ratio in the internal combustion engine, may be temporarily controlled to the stoichiometric ratio, depending on engine operating conditions.
[0017] With the above arrangements, the NOx adsorbing capability and NOx conversion efficiency of the NOx storage-reduction catalyst can be enhanced.
BRIEF DESCRIPTION OF THE DRAWINGS
[0018] The foregoing and further features and advantages of the invention will become apparent from the following description of example embodiments with reference to the accompanying drawings, wherein like numerals are used to represent like elements, and wherein;
FIG. 1 is an overall view of an internal combustion engine; FIG. 2 is a cross-sectional view of a NOx storage-reduction catalyst; FIG. 3A and FIG. 3B are cross- sectional views of a surface portion of a catalyst support; FIG. 4 is an enlarged cross-sectional view of the NOx storage -reduction catalyst;
FIG. 5A through FIG. 5 C are views showing various examples of NOx storage -reduction catalysts; FIG. 6A and FIG. 6B are views showing various examples of three-way catalysts;
FIG. 7 is a view useful for explaining a predetermined load factor KLX;
FIG. 8 is a flowchart illustrating an engine operation control routine;
FIG. 9A through FIG. 9C are view showing various experimental results; and
FIG. 10 is a view useful for explaining a peak value of a discharged NOx amount.
DETAILED DESCRIPTION OF EMBODIMENTS [0019] FIG. 1 illustrates the case where the invention is applied to a spark ignition type internal combustion engine. The invention may also be applied to a compression ignition type internal combustion engine.
[0020] Referring to FIG. 1, the spark ignition type internal combustion engine includes an engine body 1, cylinder block 2, cylinder head 3, piston 4, combustion chamber 5, intake valve 6, intake port 7, exhaust valve 8, exhaust port 9, and a spark plug 10. The intake port 7 of each cylinder is connected to a surge tank 12 via a corresponding intake branch pipe 11. The surge tank 12 is connected to an air cleaner 14 via an intake duct 13. An air flow meter 15 and a throttle valve 17 adapted to be driven by a step motor 16 are disposed in the intake duct 13. A fuel injection valve 18 is mounted to the intake port 7 of each cylinder. The fuel injection valve 18 for each cylinder is connected to a common rail 19, and the common rail 19 is connected to a fuel tank 21 via a fuel pump 20 capable of controlling the amount of fuel delivered therefrom. A fuel pressure sensor 22 is mounted to the common rail 19, and the amount of fuel delivered from the fuel pump 20 is controlled so that the fuel pressure in the common rail 19 becomes equal to a target pressure.
[0021] On the other hand, the exhaust port 9 of each cylinder is connected to a casing 25 via an exhaust manifold 23 and an exhaust pipe 24, and the casing 25 is connected to an exhaust pipe 26. An air-fuel ratio sensor 27 is mounted in the exhaust pipe 24, and a catalyst 28 is housed in the casing 25.
[0022] An electronic control unit 30 consists of a digital computer, and includes ROM (read-only memory) 32, RAM (random access memory) 33, CPU (microprocessor) 33, input port 35, and output port 36, which are connected to each other via a bidirectional bus 31. A load sensor 40 that produces an output voltage proportional to the amount of depression of an accelerator pedal 39 is connected to the accelerator pedal 39. The input port 35 receives output voltages of the air flow meter 15, fuel pressure sensor 22, air-fuel ratio sensor 27 and the load sensor 40, via corresponding A/D converters 37. A crank angle sensor 41 produces an output pulse each time the crankshaft rotates, for example, 30°, and the output pulse is transmitted to the input port 35. The CPU 34 calculates the engine speed Ne, based on the output pulses received from the crank angle sensor 41. On the other hand, the output port 36 is connected to the spark plug 10, step motor 16, fuel injection valve 18, and the fuel pump 20, via corresponding driving circuits 38. [0023] The catalyst 28 includes an upstream catalyst 28U and a downstream catalyst 28D which are arranged in series with each other in the casing 25. In one embodiment of the invention, the upstream catalyst 28U consists of a NOx storage-reduction catalyst, and the downstream catalyst 28D consists of a three-way catalyst. However, the downstream catalyst 28D may consist of a NOx storage -reduction catalyst. In this embodiment of the invention, the capacity of the upstream catalyst 28U is made equal to or larger than that of the downstream catalyst 28D. However, the capacity of the upstream catalyst 28U may be made smaller than that of the downstream catalyst 28D.
[0024] FIG. 2 illustrates the structure of the upstream catalyst, or NOx storage -reduction catalyst 28U. In the embodiment shown in FIG. 2, the NOx storage -reduction catalyst 28U has a honeycomb structure, and includes a plurality of exhaust gas channels 51 that are separated from each other by thin partition walls 50. A catalyst support 55 made of, for example, alumina is loaded on the opposite surfaces of each partition wall, or substrate 50. FIG. 3A and FIG. 3B schematically illustrate a cross-section of a surface portion of the catalyst support 55. As shown in FIG. 3A and FIG. 3B, a noble-metal catalyst 56 is supported, while being scattered, on the surface of the catalyst support 55, and a layer of a NOx absorbent 57 is formed on the surface of the catalyst support 55. [0025] At least one selected from platinum (Pt), palladium (Pd), osmium
(Os), gold (Au), rhodium (Rh), iridium (Ir), and ruthenium (Ru) is used as the noble-metal catalyst 56. As a component that constitutes the NOx absorbent 57, at least one selected from alkali metals, such as potassium (Iv), sodium (Na), and cesium (Cs), alkaline earths, such as barium (Ba) and calcium (Ca), and rare earths, such as lanthanum (La) and yttrium (Y). is used.
[0026] Where the ratio of air and fuel (hydrocarbon) supplied into the engine intake passage, combustion chamber 5 and the exhaust passage upstream of the NOx storage -reduction catalyst 28U is referred to as "air-fuel ratio of exhaust gas", the NOx absorbent 57 performs NOx absorbing and releasing functions to absorb NOx when the air-fuel ratio of exhaust gas is lean, and release the absorbed NOx when the concentration of oxygen in the exhaust gas is reduced.
[0027] In the case where platinum (Pt) is used as the noble-metal catalyst
56, and barium (Ba) is used as a component that constitutes the NOx absorbent 57, by waj' of example, when the air-fuel ratio of exhaust gas is lean, namely, when the concentration of oxygen in the exhaust gas is high, NOx contained in the exhaust gas is oxidized into NO2 on the platinum (Pt) 56 as shown in FIG. 3A, and NO2 is then absorbed into the NOx absorbent 57, to be dispersed in the form of nitrate ions NO3' in the NOx absorbent 57 while combining with barium carbonate (BaCOa). In this manner, NOx is absorbed into the NOx absorbent 57. NO2 is produced on the surface of the platinum (Pt) 56 as long as the concentration of oxygen in the exhaust gas is sufficiently high, and NO2 is absorbed into the NOx absorbent 57 to form nitrate ions NO3' as long as the NOx absorbing capability of the NOx absorbent 57 is not saturated. [0028] If the air-fuel ratio of the exhaust gas turns rich, on the other hand, the concentration of oxygen in the exhaust gas is reduced, and the reaction proceeds in the reverse direction (NO3' -» NO 2), so that nitrate ions NO3' in the NOx absorbent 57 are released in the form of NO2 from the NOx absorbent 57, as shown in FIG. 3B. Then, the released NOx is reduced by unburned HC and CO contained in the exhaust gas.
[0029] In this embodiment of the invention, the NOx storage-reduction catalyst 28U has a multi-layer structure including an upper layer 28UU and a lower layer 28UL, as shown in FIG. 4. Namely, the lower layer 28UL and the upper layer 28UU are successively laminated on the substrate 50. In this case, each of the upper layer 28UU and the lower layer 28LHL provides a NOx storage -reduction catalyst, namely, includes the above "described noble-metal catalyst 56 and NOx absorbent 57. An additional layer may be provided between the upper layer 28LTU and the lower layer 2SL7L, or between the lower layer 28L1L and the catalyst support 55. [0030] At least one selected from noble metals having a high oxidizing capability, such as platinum (Pt), palladium (Pd), osmium (Os), and gold (Au), is used as the noble-metal catalyst 56 of the upper layer 28XJU. On the other hand, at least one selected from noble metals having a high reducing capability, such as rhodium (Rh), iridium (Ir), and ruthenium (Ru), is used as the noble-metal catalyst 56 of the lower layer 28LTL. In this case, a noble metal having a high reducing capability is not contained in the upper layer 28UU.
[0031] FIG. 5A through FIG. 5C show various examples of the noble-metal catalysts 58 of the upper layer 28ULi and the lower layer 28LTL. As the noble-metal catalyst 56 of the upper layer 28UU, platinum (Pt) is used in the example of FIG. 5A, and palladium (Pd) is used in the example of FIG. 5B, while platinum (Pt) and palladium (Pd) are used in the example of FIG. 5C. On the other hand, rhodium (Rh) is used as the noble-metal catalyst 56 of the lower layer 28UL in all of the examples of FIG. 5A- FIG. 5C. [0032] If the noble-metal catalysts 56 of the upper layer 28UU and lower layer 29UL are selected in the above manners, the oxidizing capability of the upper layer 28UU is made higher than that of the lower layer 28L7L, and the reducing capability of the lower lasher 28UL is made higher than that of the upper layer 28UU. [0033] In the meantime, the downstream catalyst, or three-way catalyst
28D also has a honeycomb structure, like the NOx storage-reduction catalyst 28LT, and includes a plurality of exhaust gas channels that are separated from each other by thin partition walls. A catalyst support made of, for example, alumina is loaded on the opposite surfaces of each partition wall, and a catalyst component including a noble-metal component is supported on the surface of the catalyst support.
[0034] In one embodiment of the invention, the three-way catalyst 28D has a multi-layer structure including an upper layer 28DU and a lower layer 28DL. In this case, each of the upper layer 28DU and the lower layer 28DL provides a three-way catalyst.
[0035] In the three-way catalyst 2SD, at least one selected from noble metals having a high reducing capability is used as a noble-metal component of the upper layer 2SDU, and at least one selected from noble metals having a high oxidizing capability is used as a noble-metal component of the lower layer 28DL. In the example shown in FIG. 6A, rhodium (Rh) is used as the noble-metal component of the upper layer 28DU, and platinum (Pt) is used as the noble-metal component of the lower layer 28DL.
[0036] If the noble -metal components of the upper layer 28DU and the lower layer 28DL are selected as described above, the reducing capability of the upper layer 28DU is made higher than that of the lower layer 28DL, and the oxidizing capability of the lower layer 28DL is made higher than that of the upper layer 28DU.
[0037] Alternatively, the three-way catalyst 28D may have a single -layer structure. In this case, at least a noble metal having a high reducing capability is used as a noble-metal component of the three-way catalyst 28D. In addition, a metal having a high oxidizing capability may be used or may not be used. In the example shown in FIG. 6B, rhodium (Rh) and platinum (Pt) are used as noble-metal components of the three-way catalyst 28D. [0038] If the noble-metal catalysts 56 of the upstream catalyst or NOx storage-reduction catalyst 28LT and the noble-metal component(s) of the downstream catalyst or three-way catalyst 28D are selected as described above, the oxidizing capability of the NOx storage -reduction catalyst 28U is made higher than that of the three-way catalyst 28D, and the reducing capability of the three-way catalyst 28D is made higher than that of the NOx storage-reduction catalyst 28LT.
[0039] In this embodiment of the invention, the upstream catalyst or NOx storage-reduction catalyst 28U and the downstream catalyst or three-way catalyst 28D are independently supported on the respective substrates, and these substrates are coupled in series with each other, thereby to form the catalyst 28. The NOx storage-reduction catalyst 28U may be supported on an upstream portion of a common substrate, and the three-way catalyst 28D may be supported on a downstream portion of the substrate.
[0040] The NOx storage-reduction catalyst 28U having a multi-layer structure is manufactured, for example, in the following manner. Here, the manufacturing method will be explained with regard to the case where rhodium (Rh) is used as the noble-metal catalyst 56 of the lower layer 28UL, and platinum (Pt) is used as the noble-metal catalyst 56 of the upper layer 28LTU. Initially, a slurry is prepared in which support powder that forms the catalyst support of the lower layer 28LTL and rhodium powder are dispersed, and the slurry is applied onto a substrate. In this case, zirconium (Zr), alumina (AI2O3), ceria (CeO2), ZrOa-Al2Os, ZrO2-AIiOs-TiOa, for example, may be used as the catalyst support of the lower layer 28UL. The rhodium powder is formed from PM powder, and is dispersed in the form of nitrate or acetate in the slurry. The viscosity of the slurry is preferably around 30%, for example, and the amount of coating preferably ranges from 50g/L to 200g/L. Then, drying (2000C, 2 hours) and firing (4000C, 4 hours) are conducted, so that the lower layer 28UL is formed.
[0041] Subsequently, a slurry is prepared in which support powder that forms the catalyst support of the upper layer 28UU and platinum powder are dispersed, and the slurry is applied onto the lower layer 28UL. In this case, zirconium (Zr), alumina (AI2O3), ceria (CeOo), AIaOs-CeOa, ZrOa-Al2Os, or ZrOa-Al2Os-TiO2, for example, may be used as the catalyst support of the upper layer 28ULT. The platinum powder is dispersed in the form of nitrate or acetate, such as tetrachi'oloplatinum or dinitroplatinum, in the sluriy. The viscosity of the slurry is preferably around 30%, for example, and the amount of coating preferably ranges from 50g/L to 200g/L. Then, drying (200°C, 2 hours) and firing (4000C, 4 hours) are conducted, so that the upper layer 28LTU is formed. In another method, a catalyst support may be first formed on the lower layer 28LTL. and the catalyst support may be impregnated with an aqueous solution of tetrachroloplatinum or dinitroplatinum.
[0042] The three-way catalyst 28D having a multi-layer structure may also be manufactured in a manner similar to the NOx storage-reduction catalyst 28U.
[0043] In the embodiment of the invention, when the engine operates at a low load with the engine load factor KL being smaller than a predetermined or preset load factor KLX as shown in FIG. 7, a lean-mode operation is performed in which an air-fuel mixture having a lean air-fuel ratio is burned. When the engine operates at a high load with the engine load factor KL being larger than the predetermined load factor IvLX, a stoichiometric-ratio operation is performed in which an air-fuel mixture having the stoichiometric ratio is burned. Here, the engine load factor IvL represents the proportion of the engine load to the full load. In this case, it may also be said that an internal combustion engine that normally operates in a lean mode (i.e., a lean-burn engine) is temporarily switched to a stoichiometricratio operation, depending on the engine operating conditions.
[0044] Thus, when the engine operates in a lean mode, the airfuel ratio of exhaust gas flowing into the NOx storage-reduction catalyst 28U becomes lean, and NOx contained in the exhaust gas is adsorbed by and stored in the NOx storage-reduction catalyst 28U. If the lean-mode operation continues to be performed, however, the NOx storage-reduction catalyst 28U adsorbs NOx to the full NOx adsorbing capability (namely, the NOx storage-reduction catalyst 28U is saturated with NOx adsorbed thereon), whereby the NOx storage-reduction catalyst 28U becomes unable to adsorb NOx any more. In the embodiment of the invention, therefore, the air-fuel ratio of the exhaust gas is temporarily made rich before the NOx storage-reduction catalyst 28U reaches the full NOx adsorbing capability (i.e.. before the NOx storage reduction catalyst 28U is saturated with NOx), so that NOx is released from the NOx storage-reduction catalyst 28U, and reduced by HC, CO in the exhaust gas, into N2, or the like.
[0045] Namely, in the embodiment of the invention, the amount of NOx adsorbed per unit time by the NOx storage-reduction catalyst 28U is stored in advance in the ROM 32, in the form of a map as a function of engine operating conditions, such as the engine load factor KL and the engine speed Ne. By integrating the NOx amount, a total value SN of the amount of NOx stored in the NOx storage-reduction catalyst 28U is calculated. Then, each time the total value SN of the stored NOx amount exceeds the upper limit MAX, a rich-mode operation is temporarily performed in which an air-fuel mixture having a rich air-fuel ratio is burned. As a result, NOx is released from the NOx storage-reduction catalyst 28U, and is reduced.
[0046] FIG. 8 illustrates a routine for implementing engine operation control according to the embodiment of the invention. This routine is executed as an interrupt at predetermined time intervals.
[0047] Referring to FIG. 8, it is initially determined in step 100 whether the engine load factor KL is larger than the predetermined load factor KLX (FIG. 7). If KL ≤ KLX, the control proceeds to step 101 in which a lean-mode operation is performed. In the following step 102, the total value SN of the stored NOx amount is calculated. In the following step 103, it is determined whether the total value SN of the stored NOx amount is larger than the upper limit MAX. If SN ≤ MAX, the current cycle of the routine of FIG. 8 ends, and the lean-mode operation is continued. If SN > MAX, on the other hand, the control proceeds to step 104, and a rich-mode operation is performed, for example, for a given period of time. In the following step 105, the total value SN of the stored NOx amount is cleared. If it is determined in step 100 that the engine load factor KL is larger than the predetermined load factor KLX, the control proceeds to step 106 in which a stoichiometric-ratio operation is performed.
[0048] According to the embodiment of the invention, the NOx adsorbing capability of the catalyst 28 or the NOx storage-reduction catalyst 28U can be enhanced.
[0049] FIG. 9A shows experimental results on the NOx storage capacity ST of the catalyst 28. In Comparative Example Ca shown in FIG. 9A, the catalyst 28 consists solely of a NOx storage -reduction catalyst having a single-layer structure, and platinum (Pt) and rhodium (Rh) are used as a noble-metal catalyst. In Example EaI, the catalyst 28 consists solely of a NOx storage-reduction catalyst having a double-layer structure, and platinum (Pt) is used as a noble-metal catalyst of the upper layer while rhodium (Rh) is used as a noble-metal catalyst of the lower layer. In Example Ea2, the catalyst 28 consists solely of a NOx storage-reduction catalyst having a double-layer structure, and platinum (Pt) and palladium (Pd) are used as a noble-metal catalyst of the upper layer while rhodium (Rh) is used as a noble-metal catalyst of the lower layer. [0050] As is understood from FIG. 9A, the NOx storage capacity ST of the catalyst 28 is relatively large in Examples EaI, Ea2, and is larger in Example Ea2 than in Example EaI. This may be because the NOx storage-reduction catalyst has a multi-layer structure, namely, consists of two laj^ers. Accordingly, the frequency at which the air-fuel ratio of exhaust gas flowing into the catalyst 28 is switched to the rich side (on which the air-fuel ratio is smaller than the stoichiometric ratio) can be reduced, and fuel consumption (i.e., the amount of fuel consumed) can be reduced.
[0051] When the air-fuel ratio A/F of the exhaust gas flowing into the catalyst 28 is switched to the rich side as shown in FIG. 10, the amount EXN of
NOx discharged from the catalyst 28 per unit time rapidly increases, reaches its peak value PIvN, and then decreases. In the embodiment of the invention, the peak value PKN of the discharged NOx amount EXN can be reduced.
[0052] FIG. 9B shows experimental results on the peak value PKN of the discharged NOx amount of the catalyst 28. In Comparative Example CbI shown in FIG. 9B, the catalyst 28 consists solely of a NOx storage-reduction catalyst having a single-layer structure, and platinum (Pt) and rhodium (Rh) are used as a noble-metal catalyst. In Comparative Example Cb2, the catalyst 28 consists solely of a NOx storage -reduction catalyst having a double-layer structure, and platinum (Pt) is used as a noble-metal component of the upper layer while rhodium
(Rh) is used as a noble-metal component of the lower layer. In Example Eb, the catalyst 28 consists of an upstream catalyst and a downstream catalyst. The upstream catalyst consists of a NOx storage-reduction catalyst having a double-layer structure, and platinum (Pt) is used as a noble-metal catalyst of the upper layer while rhodium (Rh) is used as a noble-metal catalyst of the lower layer.
The downstream catalyst consists of a three-way catalyst having a single-layer structure, and platinum (Pt) and rhodium (Rh) are used as noble-metal components.
[0053] As is understood from FIG. 9B, the peak value PKN of the discharged NOx amount is larger in Comparative Example Cb2 than that of Comparative Example CbI. In Example Eb, however, the peak value PKN of the discharged NOx amount can be significantly reduced. This may be because NOx released from the upstream catalyst or NOx storage-reduction catalyst is reduced by the downstream catalyst. Accordingly, the NOx conversion efficiency can be held at a high level during lean-mode operation while assuring a large NOx storage capacity.
[0054] Furthermore, according to the embodiment of the invention, the NOx conversion efficiency EFFS of the catalyst 28 can be held at a high level when the air-fuel ratio of exhaust gas flowing into the catalyst 28 is substantially equal to the stoichiometric ratio, for example, during high-load operation.
[0055] FIG. 9C shows experimental results on the NOx conversion efficiency EFFS of the catalyst 28 when the air-fuel ratio of the incoming exhaust gas is substantially equal to the stoichiometric ratio. In Comparative Example CcI shown in FIG. 9C, the catalyst 28 consists solely of a NOx storage -reduction catalyst having a single-layer structure, and platinum (Pt) and rhodium (Rh) are used as a noble-metal catalyst. In Comparative Example Cc2, the catalyst 28 consists solely of a three-way catafyst having a double-layer structure, and rhodium (Rh) is used as a noble-metal catalyst of the upper layer while platinum (Pt) is used as a noble-metal catalyst of the lower layer. In Example Ec, the catalyst 28 consists of an upstream catalyst and a downstream catalyst. The upstream catalyst consists of a NOx storage-reduction catalyst having a double-layer structure, and platinum (Pt) is used as a noble-metal catalyst of the upper layer while rhodium (Rh) is used as a noble-metal catalyst of the lower layer. The downstream catalyst consists of a three-way catalyst having a single-layer structure, and platinum (Pt) and rhodium (Rh) are used as noble-metal components. Where INN represents the amount of NOx flowing into the catalyst 28 per unit time, and EXN represents the amount of NOx flowing out of the catalyst 28, the NOx conversion efficiency EFFS of the catalyst 28 may be expressed by the following equation:
[0056] EFFS = (INN - EXN) / INN
As is understood from FIG. 9C, the NOx conversion efficiency EFFS of Example Ec is higher than that of Comparative Example CcI, and is substantially equal to that of Comparative Example of Cc2.
[0057] In the embodiment of the invention as described above, a rich-mode operation (i.e., operating the engine at a rich air-fuel ratio) is performed so as to make the air-fuel ratio of exhaust gas flowing into the NOx storage-reduction catalyst 28U rich. However, in an internal combustion engine provided with fuel injection valves through which fuel is directly injected into combustion chambers, the aii-fuel ratio of the incoming exhaust gas may be made rich by injecting fuel into the combustion chamber during the expansion stroke or exhaust stroke. It is also possible to make the air-fuel ratio of the incoming exhaust gas rich by supplying a reductant or secondary fuel into an exhaust passage upstream of the NOx storage-reduction catalyst 28U.
[0058] In the embodiment of the invention as described above, a lean-mode operation is performed when the engine operates at a low load, and a stoichiometrkrratio operation is performed when the engine operates at a high load. However, a stoichiometricratio operation may also be performed during acceleration.
[0059] While the invention has been described with reference to example embodiments thereof, it is to be understood that the invention is not limited to the described embodiments or constructions. To the contrary, the invention is intended to cover various modifications and equivalent arrangements. In addition, while the various elements of the example embodiments are shown in various combinations and configurations, other combinations and configurations, including more, less or only a single element, are also within the spirit and scope of the invention.

Claims

CLAIMS:
1. An exhaust purifying device of an internal combustion engine, wherein an upstream catalyst and a downstream catalyst are arranged in series with each other and are housed in a common casing disposed in an engine exhaust passage, characterized in that: the upstream catalyst comprises a NOx storage -reduction catalyst that adsorbs NOx contained in incoming exhaust gas when the air-fuel ratio of the incoming exhaust gas is lean, and releases and reduces the adsorbed NOx when the air-fuel ratio of the incoming exhaust gas becomes rich, and the downstream catalyst comprises one of a three-way catalyst and a NOx storage-reduction catatyst; the upstream catalyst and the downstream catalyst are prepared such that the upstream catalyst has a higher oxidizing capability than the downstream catalyst, and such that the downstream catalyst has a higher reducing capability than the upstream catalyst; and the upstream catalyst has a multi-layer structure including an upper layer and a lower layer, and is prepared such that the upper layer has a higher oxidizing capability than the lower layer, and such that the lower layer has a higher reducing capability than the upper layer.
2. The exhaust purifying device according to claim 1, wherein each of the upper laj^er and the lower layer of the upstream catalyst contains both of a noble-metal catalyst comprising at least one selected from platinum (Pt), palladium (Pd), osmium (Os), gold (Au), rhodium (Rh), iridium (Ir), and ruthenium (Ru), and a NOx absorbent comprising at least one selected from alkali metals, alkaline earths, and rare earths.
3. The exhaust purifying device according to claim 2, wherein: the upper layer of the upstream catalyst contains, as the noble-metal catalyst, at least one selected from platinum (Pt), palladium (Pd), osmium (Os), and gold (Au); and the lower layer of the upstream catalyst contains, as the noble-metal catalyst, at least one selected from rhodium (Rh), iridium (Ir), and ruthenium (Ru).
4. The exhaust purifying device according to any one of claims 1 to 3, wherein the downstream catalyst has a multi-layer structure including an upper layer and a lower layer, and is prepared such that the upper layer has a higher reducing capability than the lower layer, and the lower layer has a higher oxidizing capability than the upper layer.
5. The exhaust purifying device according to claim 4, wherein: rhodium (Rh) is used as a noble-metal component of the upper layer of the downstream catalyst; and platinum (Pt) is used as a noble-metal component of the lower layer of the downstream catalyst.
6. The exhaust purifying device according to any one of claims 1 to 3, wherein the downstream catalyst has a single-layer structure.
7. The exhaust purifying device according to claim 6, wherein the downstream catalyst contains rhodium (Rh) and platinum (Pt) as noble-metal components.
8. The exhaust purifying device according to any one of claims 1 to 7, wherein^ the air-fuel ratio in the internal combustion engine is normally set to a lean air-fuel ratio that is larger than a stoichiometric ratio; and when NOx stored in the NOx storage-reduction catalyst is to be released and reduced, the air-fuel ratio of exhaust gas flowing into the NOx storage -reduction catalyst is temporarily controlled to a rich air-fuel ratio that is smaller than the stoichiometric ratio.
9. The exhaust purifying device according to claim 8, wherein the aii"fuel ratio in the internal combustion engine is temporarily controlled to the stoichiometric ratio, depending on engine operating conditions.
PCT/IB2008/002964 2007-11-07 2008-11-06 Exhaust purifying device of internal combustion engine WO2009060290A2 (en)

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JP2009114994A (en) 2009-05-28
WO2009060290A3 (en) 2009-06-25

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