US20060075740A1 - Spark ignition engine including three-way catalyst with nox storage component - Google Patents
Spark ignition engine including three-way catalyst with nox storage component Download PDFInfo
- Publication number
- US20060075740A1 US20060075740A1 US10/515,529 US51552905A US2006075740A1 US 20060075740 A1 US20060075740 A1 US 20060075740A1 US 51552905 A US51552905 A US 51552905A US 2006075740 A1 US2006075740 A1 US 2006075740A1
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- United States
- Prior art keywords
- engine
- twc
- engine according
- nox
- nox storage
- Prior art date
- Legal status (The legal status 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 status listed.)
- Abandoned
Links
- 239000003054 catalyst Substances 0.000 title claims abstract description 70
- 239000000446 fuel Substances 0.000 claims abstract description 61
- 230000004044 response Effects 0.000 claims abstract description 10
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical group [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 26
- 239000007789 gas Substances 0.000 claims description 22
- 229930195733 hydrocarbon Natural products 0.000 claims description 21
- 150000002430 hydrocarbons Chemical class 0.000 claims description 21
- 239000000203 mixture Substances 0.000 claims description 19
- 239000010948 rhodium Substances 0.000 claims description 18
- 238000002347 injection Methods 0.000 claims description 13
- 239000007924 injection Substances 0.000 claims description 13
- 239000003502 gasoline Substances 0.000 claims description 9
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 8
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 7
- 229910052697 platinum Inorganic materials 0.000 claims description 7
- 229910052703 rhodium Inorganic materials 0.000 claims description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 6
- 230000032683 aging Effects 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 6
- 239000001301 oxygen Substances 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 238000011144 upstream manufacturing Methods 0.000 claims description 6
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 5
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 5
- CETPSERCERDGAM-UHFFFAOYSA-N ceric oxide Chemical compound O=[Ce]=O CETPSERCERDGAM-UHFFFAOYSA-N 0.000 claims description 5
- 229910000422 cerium(IV) oxide Inorganic materials 0.000 claims description 5
- 229910052746 lanthanum Inorganic materials 0.000 claims description 5
- FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical compound [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 claims description 5
- 229910052761 rare earth metal Inorganic materials 0.000 claims description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 4
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 4
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 4
- 229910052783 alkali metal Inorganic materials 0.000 claims description 4
- 150000001340 alkali metals Chemical class 0.000 claims description 4
- 229910052748 manganese Inorganic materials 0.000 claims description 4
- 239000011572 manganese Substances 0.000 claims description 4
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 229910052763 palladium Inorganic materials 0.000 claims description 4
- 229910052726 zirconium Inorganic materials 0.000 claims description 4
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 3
- 239000004215 Carbon black (E152) Substances 0.000 claims description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 3
- 229910052791 calcium Inorganic materials 0.000 claims description 3
- 239000011575 calcium Substances 0.000 claims description 3
- 239000003915 liquefied petroleum gas Substances 0.000 claims description 3
- 229910052749 magnesium Inorganic materials 0.000 claims description 3
- 239000011777 magnesium Substances 0.000 claims description 3
- 239000003345 natural gas Substances 0.000 claims description 3
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims description 3
- 239000003381 stabilizer Substances 0.000 claims description 3
- 229910052712 strontium Inorganic materials 0.000 claims description 3
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 229910052779 Neodymium Inorganic materials 0.000 claims description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 2
- 229910052777 Praseodymium Inorganic materials 0.000 claims description 2
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 2
- 229910052782 aluminium Inorganic materials 0.000 claims description 2
- 239000004411 aluminium Substances 0.000 claims description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 2
- 229910052788 barium Inorganic materials 0.000 claims description 2
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims description 2
- 229910052792 caesium Inorganic materials 0.000 claims description 2
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- 239000002826 coolant Substances 0.000 claims description 2
- 229910052741 iridium Inorganic materials 0.000 claims description 2
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 claims description 2
- QEFYFXOXNSNQGX-UHFFFAOYSA-N neodymium atom Chemical compound [Nd] QEFYFXOXNSNQGX-UHFFFAOYSA-N 0.000 claims description 2
- GNRSAWUEBMWBQH-UHFFFAOYSA-N nickel(II) oxide Inorganic materials [Ni]=O GNRSAWUEBMWBQH-UHFFFAOYSA-N 0.000 claims description 2
- 229910052762 osmium Inorganic materials 0.000 claims description 2
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 claims description 2
- -1 perovskites Inorganic materials 0.000 claims description 2
- 229910052700 potassium Inorganic materials 0.000 claims description 2
- 239000011591 potassium Substances 0.000 claims description 2
- PUDIUYLPXJFUGB-UHFFFAOYSA-N praseodymium atom Chemical compound [Pr] PUDIUYLPXJFUGB-UHFFFAOYSA-N 0.000 claims description 2
- 229910052707 ruthenium Inorganic materials 0.000 claims description 2
- 229910052727 yttrium Inorganic materials 0.000 claims description 2
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 claims description 2
- 150000002910 rare earth metals Chemical class 0.000 claims 3
- 150000002602 lanthanoids Chemical group 0.000 claims 1
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 249
- 230000000052 comparative effect Effects 0.000 description 15
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 12
- 229910002091 carbon monoxide Inorganic materials 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 10
- 230000008901 benefit Effects 0.000 description 9
- 238000012360 testing method Methods 0.000 description 8
- 239000000758 substrate Substances 0.000 description 7
- 229910052593 corundum Inorganic materials 0.000 description 6
- 230000009467 reduction Effects 0.000 description 6
- 229910001845 yogo sapphire Inorganic materials 0.000 description 6
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 238000011068 loading method Methods 0.000 description 5
- 238000007254 oxidation reaction Methods 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 230000001133 acceleration Effects 0.000 description 4
- 238000002485 combustion reaction Methods 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 229910002651 NO3 Inorganic materials 0.000 description 3
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- MCMNRKCIXSYSNV-UHFFFAOYSA-N ZrO2 Inorganic materials O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 3
- 239000010970 precious metal Substances 0.000 description 3
- 230000008929 regeneration Effects 0.000 description 3
- 238000011069 regeneration method Methods 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- 150000001341 alkaline earth metal compounds Chemical class 0.000 description 2
- 239000010953 base metal Substances 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 230000001172 regenerating effect Effects 0.000 description 2
- 238000009420 retrofitting Methods 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- 229910052684 Cerium Inorganic materials 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- ZMIGMASIKSOYAM-UHFFFAOYSA-N cerium Chemical compound [Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce] ZMIGMASIKSOYAM-UHFFFAOYSA-N 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- 230000001351 cycling effect Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000002638 heterogeneous catalyst Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- MRELNEQAGSRDBK-UHFFFAOYSA-N lanthanum(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[La+3].[La+3] MRELNEQAGSRDBK-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 229910003158 γ-Al2O3 Inorganic materials 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation 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
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/92—Chemical or biological purification of waste gases of engine exhaust gases
- B01D53/94—Chemical or biological purification of waste gases of engine exhaust gases by catalytic processes
- B01D53/9445—Simultaneously removing carbon monoxide, hydrocarbons or nitrogen oxides making use of three-way catalysts [TWC] or four-way-catalysts [FWC]
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01N—GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
- F01N3/00—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust
- F01N3/08—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation 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
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/92—Chemical or biological purification of waste gases of engine exhaust gases
- B01D53/94—Chemical or biological purification of waste gases of engine exhaust gases by catalytic processes
- B01D53/9495—Controlling the catalytic process
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01N—GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
- F01N3/00—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust
- F01N3/08—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous
- F01N3/0807—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous by using absorbents or adsorbents
- F01N3/0814—Exhaust 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
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01N—GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
- F01N3/00—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust
- F01N3/08—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous
- F01N3/0807—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous by using absorbents or adsorbents
- F01N3/0828—Exhaust 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
- F01N3/0842—Nitrogen oxides
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
- F02D—CONTROLLING COMBUSTION ENGINES
- F02D41/00—Electrical control of supply of combustible mixture or its constituents
- F02D41/02—Circuit arrangements for generating control signals
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
- F02D—CONTROLLING COMBUSTION ENGINES
- F02D41/00—Electrical control of supply of combustible mixture or its constituents
- F02D41/02—Circuit arrangements for generating control signals
- F02D41/021—Introducing corrections for particular conditions exterior to the engine
- F02D41/0235—Introducing corrections for particular conditions exterior to the engine in relation with the state of the exhaust gas treating apparatus
- F02D41/027—Introducing corrections for particular conditions exterior to the engine in relation with the state of the exhaust gas treating apparatus to purge or regenerate the exhaust gas treating apparatus
- F02D41/0275—Introducing corrections for particular conditions exterior to the engine in relation with the state of the exhaust gas treating apparatus to purge or regenerate the exhaust gas treating apparatus the exhaust gas treating apparatus being a NOx trap or adsorbent
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01N—GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
- F01N2570/00—Exhaust treating apparatus eliminating, absorbing or adsorbing specific elements or compounds
- F01N2570/16—Oxygen
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
- F02D—CONTROLLING COMBUSTION ENGINES
- F02D2200/00—Input parameters for engine control
- F02D2200/02—Input parameters for engine control the parameters being related to the engine
- F02D2200/08—Exhaust gas treatment apparatus parameters
- F02D2200/0806—NOx storage amount, i.e. amount of NOx stored on NOx trap
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/20—Air quality improvement or preservation, e.g. vehicle emission control or emission reduction by using catalytic converters
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02T—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
- Y02T10/00—Road transport of goods or passengers
- Y02T10/10—Internal combustion engine [ICE] based vehicles
- Y02T10/12—Improving ICE efficiencies
Definitions
- the present invention relates to a spark ignition engine comprising an exhaust system comprising a catalyst and an engine control unit programmed to control the air-to-fuel ratio of the engine to run at the stoichiometric air-to-fuel ratio during normal running conditions and to run lean of the stoichiometric air-to-fuel ratio during a defined portion of an engine speed/load map.
- the present invention relates to such an engine wherein the catalyst is a three-way catalyst (TWC) including a NOx storage component.
- TWC three-way catalyst
- a heterogeneous catalyst capable of simultaneous conversion of nitrogen oxides (NOx), carbon monoxide (CO) and unburnt hydrocarbons (HC) in exhaust gas from a stoichiometrically operated, spark-ignited combustion engine is known as a three-way catalyst (TWC).
- NOx reduction readily occurs over the TWC when the air-to-fuel ratio is rich of stoichiometric, whereas CO and HC reactions are hindered by insufficient oxygen (O 2 ).
- O 2 oxygen
- the CO and HC conversions are high, but NOx reduction is difficult because of the excess of oxidising species. Accordingly, effective three-way conversion occurs in a relatively narrow air-to-fuel ratio window.
- an oxygen sensor is used to detect the lambda composition of the exhaust gas upstream of the TWC and to adjust the air-to-fuel ratio accordingly to equilibrate the exhaust gas.
- a typical TWC comprises platinum (Pt) and/or palladium (Pd) as an oxidation catalyst and rhodium (Rh) as a reduction catalyst on a suitable high surface area oxide support, such as alumina (AM 2 O 3 ), and an oxygen storage component (OSC), e.g. a ceria-zirconia mixed oxide.
- a suitable high surface area oxide support such as alumina (AM 2 O 3 )
- an oxygen storage component e.g. a ceria-zirconia mixed oxide.
- Various minor amounts of base metal catalyst promoters, stabilisers and hydrogen sulphide suppressers can be included. For flirter details, see WO 98/03251 (incorporated herein by reference).
- This component adsorbs (or absorbs) O 2 in the lean environment and releases it in the rich environment, thus effectively extending the time at which the exhaust gas is at the set point Where more significant amounts of HC fuel are required to maintain the air-to-fuel ratio, such as during acceleration, this can be provided e.g. by adjusting the fuel injection period.
- a typical NOx trap composition comprises Pt and Rh on a high surface area oxide support, such as Al 2 O 3 , and a NOx storage component such as barium oxide (BaO (see, e.g. EP 0758713, incorporated herein by reference)).
- a NOx storage component such as barium oxide (BaO (see, e.g. EP 0758713, incorporated herein by reference)
- loadings of NOx storage components in NOx trap washcoats can be up to 50 wt % or even higher
- NOx trap technology requires very careful and complicated control of the engine in order to provide for rich regeneration of the NOx storage component
- a number of feedback sensors are used to control the function of the NOx trap NOx storage capacity, e.g. sensors to estimate cumulative engine-out NOx production utilising stored engine maps and NOx trap temperature sensors, because the efficiency of the NOx storage component to absorb NOx is temperature dependent.
- Base metal catalyst promoters such as barium (Ba), cerium, lanthanum, magnesium, calcium and strontium can also be used (see WO 98/03251, mentioned above).
- the catalytic converter for a lean burn internal combustion engine, such as a direct injection gasoline engine, comprising a catalyst component capable of storing NOx.
- the catalytic converter comprises a supported layered catalyst having a first, inner layer containing a first platinum group metal (PGM), e.g. Pt, and a NOx storage component, e.g. Ba, and a second, outer layer containing a second different PGM, such as Rh supported on a non-Al 2 O 3 support, and optionally an OSC such as a mixed oxide of ceria and zirconia.
- PGM platinum group metal
- Japanese Unexamined Patent Publication (KOKAI) No. 5-317,652 (incorporated herein by reference) describes a catalyst comprising a substrate, and an alkaline-earth metal compound and Pt loaded on the substrate.
- the gasoline engine is run on the fuel lean side, such as an air-to-fuel ratio of up to 23:1 (wt./wt.).
- the catalyst is designed to adsorb (or absorb) NOx on the alkaline-earth metal during lean running conditions and to use the natural fluctuation of the air-to-fuel ratio to the rich side to enable stored NOx to be released and reduced, thus regenerating the NOx storage capacity of the alkaline-earth metal compound.
- spark ignition engine such as a port fuel injection gasoline engine, which engine comprising a TWC including a NOx storage component, in such a way as to benefit from the increased fuel economy available during lean running conditions whilst avoiding the requirement for expensive and complicated control systems.
- the invention provides A spark ignition engine comprising an exhaust system comprising a catalyst and an engine control unit programmed to control the air-to-fuel ratio of the engine to run at the stoichiometric air-to-fuel ratio during normal running conditions and to run lean of the stoichiometric air-to-fuel ratio during a defined portion of an engine speed/load map, which catalyst comprising a three-way catalyst (TWC) including a NOx storage component, characterised in that the engine control unit is further programmed to determine the amount of NOx contacting the TWC during lean running operation in response to data input from sensor means, thereby to determine the remaining NOx storage capacity of the TWC and to return the air-to-fuel ratio to stoichiometry when the remaining NOx storage capacity is below a pre-determined value, the arrangement being such as to substantially prevent passing more NOx to atmosphere during an engine cycle compared with a spark ignition engine run continuously in stoichiometric mode.
- TWC three-way catalyst
- engine cycle herein we mean the period between key on and key off.
- the present invention takes advantage of the natural fluctuation in the composition of an exhaust gas of a spark ignition engine operated at the stoichiometric air-to-fuel ratio to rich lambda values, e.g. during acceleration, to regenerate the NOx storage component.
- a catalyst that facilitates the regeneration of a NOx storage component in a TWC, which catalyst is used in a preferred embodiment according to the invention.
- the present invention provides a number of very substantial advantages.
- One such advantage is that it enables a vehicle powered by a spark ignition engine to be run at a fuel saving over a similar vehicle operated continuously at substantially stoichiometric conditions.
- Such increased efficiency can result in lower CO 2 emissions in a legislative test cycle for a vehicle.
- Lower CO 2 emissions in a legislative test cycle translates to lower CO 2 emissions in “real world” driving conditions.
- a vehicle according to the invention can be more “environmentally friendly”.
- countries where vehicles are taxed depending on the amount of CO 2 they emit (a so-called “green tax”), such as the UK, it can reduce the tax burden to the consumer.
- a second such advantage is that it can allow existing vehicles including spark ignition engines to receive the benefit of the invention by retrofitting certain components. This can be done by simply replacing the existing TWC with a TWC including sufficient NOx storage component and the engine control unit for one programmed: (i) to run the engine lean of the stoichiometric air-to-fuel ratio during a defined portion of an engine speed/load map; and (ii) to determine the amount of NOx contacting the TWC during lean running operation in response to data input from sensor means, thereby to determine the remaining NOx storage capacity of the TWC and to return the air-to-fuel ratio to stoichiometry when the remaining NOx storage capacity is below a pre-determined value, thereby substantially to prevent passing more NOx to atmosphere during an engine cycle compared with a spark ignition engine run continuously in stoichiometric mode.
- the defined portion of the engine speed/load map is engine idle.
- the defined portion of the engine speed/load map can comprise low speed driving wherein the level of NOx emitted by the engine is up to ten times more, such as five times or twice more, than at engine idle.
- a very substantial advantage of this preferred arrangement is that it avoids the requirement for complicated and expensive sensors and controls in order to meet emission legislation that presently burdens the adoption of NOx traps.
- a number of means for inputting data to the engine control unit to determine the amount of NOx contacting the TWC, and hence the remaining NOx storage capacity of the NOx storage component, can be used either singly or in any mechanically/electronically viable combination.
- Many of the sensor means required to collect this information are already included in the engine and/or vehicle fitted with the engine and are used by the engine control unit for controlling other functions of the engine and/or vehicle. This is one reason why it is possible to adopt the invention by retrofitting the vehicle engine control unit, together with a TWC including a NOx storage component.
- Such detected data that can be used to monitor remaining NOx storage capacity in the TWC of the invention include: predetermined or predicted time elapsed from the start of lean running operation, by sensing the status of a suitable clock means; airflow over the TWC or manifold vacuum; ignition timing; engine speed; throttle position; exhaust gas redox composition, for example using a lambda sensor, preferably a linear lambda sensor; quantity of fuel injected in the engine; where the vehicle includes an exhaust gas recirculation (EGR) circuit, the position of the EGR valve and thereby the detected amount of EGR; engine coolant temperature; and where the exhaust system includes a NOx sensor, the amount of NOx detected upstream and/or downstream of the TWC.
- EGR exhaust gas recirculation
- the predicted time can be subsequently adjusted in response to data input.
- the spark ignition engine can be any capable of operating during normal running conditions at the stoichiometric air-to-fuel ratio.
- the engine can be powered by gasoline and the engine can be of the port fuel injection or direct injection type.
- the engine can be fuelled using an alternative fuel such as liquid petroleum gas (LPG), natural gas (NG), methanol, hydrocarbon mixtures including ethanol or hydrogen gas.
- LPG liquid petroleum gas
- NG natural gas
- methanol methanol
- hydrocarbon mixtures including ethanol or hydrogen gas hydrocarbon mixtures including ethanol or hydrogen gas.
- the invention can be used on all grades of sulfur-containing fuel, but with particular efficiency with grades containing less that 50 ppm by weight of sulfur, and most preferably less than 10 ppm by weight of sulfur.
- the present invention can utilise any known TWC composition provided that sufficient NOx storage component is included in order to perform the desired function.
- a typical TWC composition comprises at least one PGM, and can be selected from the group consisting of Pt, Pd, Rh, ruthenium, osmium and iridium and any combination of two or more thereof.
- NOx storage components are disclosed in the prior art, and any can be utilised in the present invention.
- Typical NOx storage components comprise alkali metals, such as potassium or caesium, alkaline-earth metals, e.g. magnesium, calcium, strontium or Ba, rare-earth metals lanthanide group metal, preferably La, or any viable combination, e.g. a mixed oxide, of any two or more thereof.
- a common component of state-of-the-art TWCs is the OSC and these too can be included in the TWC, with utility, according to the present invention.
- OSC an OSC assists in the combustion of HC at the stoichiometric point and slightly rich thereof.
- This property runs counter to the requirement of a system including a NOx trap composition which is to regenerate the NOx storage component using reducing species, such as HCs in the exhaust, resulting from air-to-fuel ratio modulation. Accordingly, the presence of an OSC in a NOx trap composition would cause increased fuel consumption for the same amount of NOx storage component regeneration relative to an OSC-free NOx trap composition.
- OSC include optionally stabilised ceria, perovskites, NiO, MnO 2 , manganese-based compounds supported on Al 2 O 3 -containing mixed oxides (see PCT/GB01/05124, incorporated herein by reference) a mixed oxide of manganese and zirconium (see WO 99/34904, incorporated herein by reference), Pr 2 O 3 or a combination of any two or more thereof.
- the ceria stabiliser can be zirconium, lanthanum, aluminium, yttrium, praseodymium or neodymium.
- a preferred TWC for use in the present invention comprises a first PGM, preferably Pt, and the NOx storage component in a first, inner layer and an OSC and a second PGM, preferably Rh, in a second, outer layer.
- Rh/OSC component is active for NOx reduction and other reactions while the Pt component is active for oxidation reactions.
- the Rh is relatively inactive, the Pt is active for NO, HC and CO oxidation while the NO 2 produced is stored in the adsorber as nitrate.
- the OSC component in the second layer prevents the stored NOx “seeing” reducing gas so that the NOx remains stored as nitrate.
- the Rh is active for NOx reduction by CO and the Pt is active for oxidation of HC and CO.
- the invention provides a vehicle comprising an engine according to the present invention.
- TWC are generally placed in one or both of two positions in a vehicle according to the intended purpose: the close-coupled position, in which the TWC is disposed as close to the exhaust manifold as possible; and the underfloor position.
- the reason for placing a TWC in the close-coupled position is to control emissions immediately following cold start, as much of the controlled emissions are emitted during the legislative test cycle immediately following cold-start.
- the catalyst By positioning a TWC close to the engine, the catalyst is contacted by hot exhaust gases immediately after key on and accordingly reaches the light-off temperature for CO and HC oxidation sooner than a TWC in the cooler, underfloor location.
- the underfloor catalyst shoulders much of the burden of treating the exhaust gas.
- close-coupled TWC is exposed to very high temperatures e.g. up to 1000° C. Indeed one vehicle manufacturer requires testing of close-coupled TWCs for 50 hours at catalyst bed temperatures of at least 970° C. and up to 1010° C. At these sort of temperatures, catalysts can lose activity as materials lose their surface area through sintering events, migration of active species into pores and component interactions. Accordingly, a TWC in the close-coupled position can be expected to lose some of its activity compared with a fresh catalyst.
- the NOx storage component can also lose NOx storage capacity through this high temperature ageing by loss-of surface area.
- the fresh TWC includes sufficient of the NOx storage component to retain sufficient NOx storage capacity after high temperature ageing, for example in the close-coupled position.
- the invention provides An engine control unit for a spark ignition engine comprising an exhaust system comprising a TWC including a NOx storage component, which engine control unit is programmed to control the air-to-fuel ratio of the engine to run at the stoichiometric air-to-fuel ratio during normal running conditions and to run lean of stoichiometry during a defined portion of an engine speed/load map and to determine the amount of NOx contacting the TWC during lean running operation in response to data input from sensor means, thereby to determine the remaining NOx storage capacity of the TWC and to return the air-to-fuel ratio to stoichiometry when the remaining NOx storage capacity is below a pre-determined value, the arrangement being such as to substantially prevent passing more NOx to atmosphere during an engine cycle compared with a spark ignition engine run continuously in stoichiometric mode.
- the invention provides A method of treating exhaust gas of a spark ignition engine run at the stoichiometric air-to-fuel ratio during normal running conditions, which engine comprising an exhaust system comprising a TWC including a NOx storage component, which method comprising the steps of controlling the engine air-to-fuel ratio to run lean of stoichiometry during a defined portion of an engine speed/load map and determining the amount of NOx contacting the TWC during lean running operation in response to data input from sensor means, thereby to determine the remaining NOx storage capacity of the TWC and to return the air-to-fuel ratio to stoichiometry when the remaining NOx storage capacity is below a pre-determined value, the arrangement being such as to substantially prevent passing more NOx to atmosphere during an engine cycle compared with a spark ignition engine run continuously in stoichiometric mode.
- FIG. 1 is a graph showing HC conversion against temperature after ageing of a TWC including a NOx storage component according to the invention, a state-of-the-art TWC and a NOx trap;
- FIGS. 2, 3 and 4 are graphs showing % conversion of CO, HC and NOx against lambda for a TWC including a NOx storage component according to the invention, a state-of-the-art TWC and a NOx trap formulation respectively.
- Comparative catalyst A is a state-of-the art Pt/Rh TWC on a thermally stable, high surface area support at a ratio of 5Pt:1Rh and a total precious metal loading of at 60 g ft ⁇ 3 .
- Catalyst B is a TWC including a NOx storage component according to the present invention supported on an identical substrate. It comprised a first, inner layer of a high surface area Al 2 O 3 impregnated with Pt and a NOx storage component, such as BaO, and a second, outer layer of a mixed oxide OSC impregnated with Rh. The ratio of Pt:Rh and the total precious metal loading was the same as for catalyst A.
- Comparative catalyst C is a NOx trap composition comprising a high surface area Al 2 O 3 -based mixed oxide support impregnated with Pt, Rh and a NOx storage component.
- the ratio of Pt:Rh was 6:1 and the total precious metal loading was 70 g ft ⁇ 3 .
- Each washcoat was coated on a 4.66 ⁇ 6 inch (11.9 ⁇ 15.2 cm) ceramic substrate of 400 cells per square inch ((cpsi) 62 cells cm ⁇ 2 ) of 0.15 mm wall thickness and the resulting coated substrate was hydrothermally aged at 800° C. for 5 hours under 10% O 2 /0% H 2 O balance nitrogen.
- the catalysts were fitted to the exhaust of a four cylinder 2.0 litre Port Fuel Injection bench mounted engine controlled by a Bosch ME7 control system.
- the catalyst temperature was increased by adjustment of a heat exchanger fitted to the exhaust line before the catalyst.
- the temperature ramp rate was 14° C./minute.
- the results for the HC light-off are shown in FIG. 1 , from which it can be seen that the HC light-off temperature for catalyst B is similar to that of the comparative catalyst A. It can also be seen that the HC light-off temperature of comparative catalyst C is approximately 30° C. higher than comparative catalyst A.
- the TWC including a NOx storage component (catalyst B) has very similar activity for HC activity compared with a state-of-the-art TWC (comparative catalyst A), despite the presence of the NOx storage component.
- the NOx trap (comparative catalyst C) performs less well than either catalyst B or comparative catalyst A, despite having a higher Pt loading.
- Example 2 The same engine as in Example 1 was used to give a catalyst inlet temperature of 450° C.
- the results are shown in FIGS. 2, 3 and 4 .
- the NOx trap (comparative catalyst C) is poorer for lambda scan performance (showing poorer conversion), despite having more Pt while the TWC including a NOx storage component (catalyst B) performs similarly to the TWC (comparative catalyst A).
- the engine was operated from one of two sets of maps: one for the homogeneous mode and the other for the lean, stratified mode.
- Basic maps for ignition and injection timing and duration were generated by firstly logging data from the ECU of a vehicle including the same model of engine as the one used for the bench test and then basing the maps on this information by reverse engineering.
- the lean, stratified mode was mapped by matching the torque achieved in homogeneous mode at the same speed and load demand.
- the engine Prior to testing, the engine was thoroughly warmed up in idling condition. In homogeneous mode, the engine was then run so that the inlet temperature to the close-coupled catalyst was 300° C. It was then switched to lean, stratified operation and the EGR valve position was adjusted until the engine-out NOx was 300 ppm. The EGR valve position was recorded and was referred to as the lean set point The engine was switched back to homogeneous mode, and the EGR valve was closed. A rich set point was obtained by increasing the fuel injector pulse width to obtain lambda 0.80. A series of lean/rich cycles were run as follows. In the lean mode, the EGR valve was at the lean set-point position until the NOx efficiency of the system had dropped below 75%.
- Table 1 shows the NOx storage efficiency with which each of comparative catalysts A and C and catalyst B store NOx, and in particular, how the efficiency with which each catalyst stores 30, 40, 50 and 60 mg of NOx.
- NOx trap comparative catalyst C
- TWC comparative catalyst A
- Example 1 The results of Examples 1, 2 and 3 show that the TWC including a NOx storage component maintains TWC performance despite including a NOx storage component, and that NOx storage capacity is several times higher than a state-of-the-art TWC composition.
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Abstract
A spark ignition engine with an exhaust system having a catalyst, which includes a three-way catalyst (TWC) and a NOx storage component, and an engine control unit is provided. The engine control unit is programmed to control the air-to-fuel ratio of the engine to run at the stoichiometric air-to-fuel ratio during normal running conditions and to run lean of the stoichiometric air-to-fuel ratio during a defined portion of an engine speed/load. The engine control unit also determines the amount of NOx contacting the TWC during lean running operation in response to data input from a sensor means, thereby a remaining NOx storage capacity of the TWC is determined. The control unit is programmed to return the air-to-fuel ratio to stoichiometry when the NOx storage capacity is below a pre-determined value. The engine and its components are arranged such as to substantially prevent passing more NOx to atmosphere during an engine cycle compared with a spark ignition engine run continuously at stoichiometric conditions.
Description
- The present invention relates to a spark ignition engine comprising an exhaust system comprising a catalyst and an engine control unit programmed to control the air-to-fuel ratio of the engine to run at the stoichiometric air-to-fuel ratio during normal running conditions and to run lean of the stoichiometric air-to-fuel ratio during a defined portion of an engine speed/load map. In particular, the present invention relates to such an engine wherein the catalyst is a three-way catalyst (TWC) including a NOx storage component.
- A heterogeneous catalyst capable of simultaneous conversion of nitrogen oxides (NOx), carbon monoxide (CO) and unburnt hydrocarbons (HC) in exhaust gas from a stoichiometrically operated, spark-ignited combustion engine is known as a three-way catalyst (TWC). NOx reduction readily occurs over the TWC when the air-to-fuel ratio is rich of stoichiometric, whereas CO and HC reactions are hindered by insufficient oxygen (O2). On the lean side, the CO and HC conversions are high, but NOx reduction is difficult because of the excess of oxidising species. Accordingly, effective three-way conversion occurs in a relatively narrow air-to-fuel ratio window. In practice an oxygen sensor is used to detect the lambda composition of the exhaust gas upstream of the TWC and to adjust the air-to-fuel ratio accordingly to equilibrate the exhaust gas.
- A typical TWC comprises platinum (Pt) and/or palladium (Pd) as an oxidation catalyst and rhodium (Rh) as a reduction catalyst on a suitable high surface area oxide support, such as alumina (AM2O3), and an oxygen storage component (OSC), e.g. a ceria-zirconia mixed oxide. Various minor amounts of base metal catalyst promoters, stabilisers and hydrogen sulphide suppressers can be included. For flirter details, see
WO 98/03251 (incorporated herein by reference). - A consequence of using detected oxygen concentration to control the air-to-fuel ratio is that there is a time lag associated in adjusted air-to-fuel ratio. This results in perturbation around the control set point. Thus, when operating rich, there is a need to provide a small amount of O2 to consume the unreacted CO and HC. Conversely, when the exhaust gas goes slightly oxidising, the excess O2 needs to be consumed. One development in TWC technology adopted in order to reduce the problem of emissions associated with perturbations was to incorporate an O2 storage component in the TWC composition. This component adsorbs (or absorbs) O2 in the lean environment and releases it in the rich environment, thus effectively extending the time at which the exhaust gas is at the set point Where more significant amounts of HC fuel are required to maintain the air-to-fuel ratio, such as during acceleration, this can be provided e.g. by adjusting the fuel injection period.
- More recently, there has been a move towards running gasoline combustion engines lean, for example, in gasoline direct injection engines. The rationale is to improve fuel economy (thus decreasing the emissions of CO2) by running lean of stoichiometry. The principal problem in pursuing this strategy is that the lean environment inhibits NOx reduction in the TWC. One technology which has been developed to meet this problem is called, variously, a NOx absorber/catalyst, lean NOx trap (LNT) or NOx trap and is based on acid-base washcoat chemistry. It involves adsorption (or absorption) and storage of NOx in the catalyst washcoat during lean driving conditions and release under rich operation. The released NOx is catalytically converted to nitrogen just as it is in TWCs.
- A typical NOx trap composition comprises Pt and Rh on a high surface area oxide support, such as Al2O3, and a NOx storage component such as barium oxide (BaO (see, e.g. EP 0758713, incorporated herein by reference)). Generally, loadings of NOx storage components in NOx trap washcoats can be up to 50 wt % or even higher
- A major problem with the use of NOx trap technology is that it requires very careful and complicated control of the engine in order to provide for rich regeneration of the NOx storage component Additionally, a number of feedback sensors are used to control the function of the NOx trap NOx storage capacity, e.g. sensors to estimate cumulative engine-out NOx production utilising stored engine maps and NOx trap temperature sensors, because the efficiency of the NOx storage component to absorb NOx is temperature dependent.
- It is known in the art of TWCs, to stabilise a gamma-Al2O3 component from sintering during high temperature ageing using small amounts (1-3 percent) of BaO or lanthanum oxide (La2O3). Base metal catalyst promoters, such as barium (Ba), cerium, lanthanum, magnesium, calcium and strontium can also be used (see WO 98/03251, mentioned above).
- In our WO 99/00177 (incorporated herein by reference) we describe a catalytic converter for a lean burn internal combustion engine, such as a direct injection gasoline engine, comprising a catalyst component capable of storing NOx. In one embodiment, the catalytic converter comprises a supported layered catalyst having a first, inner layer containing a first platinum group metal (PGM), e.g. Pt, and a NOx storage component, e.g. Ba, and a second, outer layer containing a second different PGM, such as Rh supported on a non-Al2O3 support, and optionally an OSC such as a mixed oxide of ceria and zirconia.
- Japanese Unexamined Patent Publication (KOKAI) No. 5-317,652 (incorporated herein by reference) describes a catalyst comprising a substrate, and an alkaline-earth metal compound and Pt loaded on the substrate. The description observes that during urban driving a vehicle is frequently accelerated and decelerated. Consequently, this can cause the air-to-fuel ratio to vary frequently from the range of values adjacent to the stoichiometric point during more steady conditions, e.g. idling, to the fuel rich side. In order to lower the fuel consumption during e.g. urban driving conditions, the gasoline engine is run on the fuel lean side, such as an air-to-fuel ratio of up to 23:1 (wt./wt.). The catalyst is designed to adsorb (or absorb) NOx on the alkaline-earth metal during lean running conditions and to use the natural fluctuation of the air-to-fuel ratio to the rich side to enable stored NOx to be released and reduced, thus regenerating the NOx storage capacity of the alkaline-earth metal compound.
- U.S. Pat. No. 5,575,983 (incorporated herein by reference) observes that the NOx absorbing capacity of the catalyst of Japanese Unexamined Patent Publication No. 5-317,652 is poisoned by sulfate. In order to combat this, it proposes a catalyst comprising Pt or Pd and alkali metals, alkaline-earth metals and rare-earth elements including lanthanum (La) supported on lithium-stabilised Al2O3.
- We believe that the use of lean burn gasoline engines other than direct injection gasoline engines, such as those described in Japanese Unexamined Patent Publication (KOKAI) No. 5-317,652 and U.S. Pat. No. 5,575,983 has not received widespread acceptance in the vehicle industry and that one reason for this is the difficulty in controlling NOx emissions to meet existing and future emission legislation.
- We have now found, very surprisingly, that it is possible to operate a spark ignition engine, such as a port fuel injection gasoline engine, which engine comprising a TWC including a NOx storage component, in such a way as to benefit from the increased fuel economy available during lean running conditions whilst avoiding the requirement for expensive and complicated control systems.
- According to one aspect, the invention provides A spark ignition engine comprising an exhaust system comprising a catalyst and an engine control unit programmed to control the air-to-fuel ratio of the engine to run at the stoichiometric air-to-fuel ratio during normal running conditions and to run lean of the stoichiometric air-to-fuel ratio during a defined portion of an engine speed/load map, which catalyst comprising a three-way catalyst (TWC) including a NOx storage component, characterised in that the engine control unit is further programmed to determine the amount of NOx contacting the TWC during lean running operation in response to data input from sensor means, thereby to determine the remaining NOx storage capacity of the TWC and to return the air-to-fuel ratio to stoichiometry when the remaining NOx storage capacity is below a pre-determined value, the arrangement being such as to substantially prevent passing more NOx to atmosphere during an engine cycle compared with a spark ignition engine run continuously in stoichiometric mode.
- By “engine cycle” herein we mean the period between key on and key off.
- The present invention takes advantage of the natural fluctuation in the composition of an exhaust gas of a spark ignition engine operated at the stoichiometric air-to-fuel ratio to rich lambda values, e.g. during acceleration, to regenerate the NOx storage component. NOx stored on the NOx storage component is generally not released, and the NOx storage component is not regenerated, under lambda=1 conditions, i.e. conditions rich of lambda=1 are required. We have also devised a catalyst that facilitates the regeneration of a NOx storage component in a TWC, which catalyst is used in a preferred embodiment according to the invention.
- The present invention provides a number of very substantial advantages. One such advantage is that it enables a vehicle powered by a spark ignition engine to be run at a fuel saving over a similar vehicle operated continuously at substantially stoichiometric conditions. Such increased efficiency can result in lower CO2 emissions in a legislative test cycle for a vehicle. Lower CO2 emissions in a legislative test cycle translates to lower CO2 emissions in “real world” driving conditions. Accordingly, a vehicle according to the invention can be more “environmentally friendly”. Furthermore, in countries where vehicles are taxed depending on the amount of CO2 they emit (a so-called “green tax”), such as the UK, it can reduce the tax burden to the consumer.
- A second such advantage is that it can allow existing vehicles including spark ignition engines to receive the benefit of the invention by retrofitting certain components. This can be done by simply replacing the existing TWC with a TWC including sufficient NOx storage component and the engine control unit for one programmed: (i) to run the engine lean of the stoichiometric air-to-fuel ratio during a defined portion of an engine speed/load map; and (ii) to determine the amount of NOx contacting the TWC during lean running operation in response to data input from sensor means, thereby to determine the remaining NOx storage capacity of the TWC and to return the air-to-fuel ratio to stoichiometry when the remaining NOx storage capacity is below a pre-determined value, thereby substantially to prevent passing more NOx to atmosphere during an engine cycle compared with a spark ignition engine run continuously in stoichiometric mode.
- According to a particularly preferred embodiment, the defined portion of the engine speed/load map is engine idle. This is a particularly advantageous arrangement in that it provides a fail-safe system for regenerating the NOx storage component This is because the only thing that can happen to the engine after idle is that it is accelerated, following which the exhaust gas contacting the TWC is temporarily rich before the engine control unit returns the exhaust gas to equivalence. Even if the engine is switched off following idle, NOx can be stored to key on, following which the engine will be accelerated. Accordingly, this preferred arrangement takes advantage of the natural fluctuations in the composition of the exhaust gas to the rich side during acceleration to regenerate the NOx storage component For similar reasons, the defined portion of the engine speed/load map can comprise low speed driving wherein the level of NOx emitted by the engine is up to ten times more, such as five times or twice more, than at engine idle.
- A very substantial advantage of this preferred arrangement is that it avoids the requirement for complicated and expensive sensors and controls in order to meet emission legislation that presently burdens the adoption of NOx traps.
- A number of means for inputting data to the engine control unit to determine the amount of NOx contacting the TWC, and hence the remaining NOx storage capacity of the NOx storage component, can be used either singly or in any mechanically/electronically viable combination. Many of the sensor means required to collect this information are already included in the engine and/or vehicle fitted with the engine and are used by the engine control unit for controlling other functions of the engine and/or vehicle. This is one reason why it is possible to adopt the invention by retrofitting the vehicle engine control unit, together with a TWC including a NOx storage component.
- Such detected data that can be used to monitor remaining NOx storage capacity in the TWC of the invention include: predetermined or predicted time elapsed from the start of lean running operation, by sensing the status of a suitable clock means; airflow over the TWC or manifold vacuum; ignition timing; engine speed; throttle position; exhaust gas redox composition, for example using a lambda sensor, preferably a linear lambda sensor; quantity of fuel injected in the engine; where the vehicle includes an exhaust gas recirculation (EGR) circuit, the position of the EGR valve and thereby the detected amount of EGR; engine coolant temperature; and where the exhaust system includes a NOx sensor, the amount of NOx detected upstream and/or downstream of the TWC. Where the clock embodiment is used, the predicted time can be subsequently adjusted in response to data input.
- The spark ignition engine can be any capable of operating during normal running conditions at the stoichiometric air-to-fuel ratio. In one embodiment, the engine can be powered by gasoline and the engine can be of the port fuel injection or direct injection type. Optionally, the engine can be fuelled using an alternative fuel such as liquid petroleum gas (LPG), natural gas (NG), methanol, hydrocarbon mixtures including ethanol or hydrogen gas. The invention can be used on all grades of sulfur-containing fuel, but with particular efficiency with grades containing less that 50 ppm by weight of sulfur, and most preferably less than 10 ppm by weight of sulfur.
- The present invention can utilise any known TWC composition provided that sufficient NOx storage component is included in order to perform the desired function.
- A typical TWC composition comprises at least one PGM, and can be selected from the group consisting of Pt, Pd, Rh, ruthenium, osmium and iridium and any combination of two or more thereof.
- Many NOx storage components are disclosed in the prior art, and any can be utilised in the present invention. Typical NOx storage components comprise alkali metals, such as potassium or caesium, alkaline-earth metals, e.g. magnesium, calcium, strontium or Ba, rare-earth metals lanthanide group metal, preferably La, or any viable combination, e.g. a mixed oxide, of any two or more thereof.
- A common component of state-of-the-art TWCs is the OSC and these too can be included in the TWC, with utility, according to the present invention. Indeed, it is trite knowledge of the person skilled in the art that NOx trap compositions do not include OSC, because an OSC assists in the combustion of HC at the stoichiometric point and slightly rich thereof. This property runs counter to the requirement of a system including a NOx trap composition which is to regenerate the NOx storage component using reducing species, such as HCs in the exhaust, resulting from air-to-fuel ratio modulation. Accordingly, the presence of an OSC in a NOx trap composition would cause increased fuel consumption for the same amount of NOx storage component regeneration relative to an OSC-free NOx trap composition.
- Known OSC include optionally stabilised ceria, perovskites, NiO, MnO2, manganese-based compounds supported on Al2O3-containing mixed oxides (see PCT/GB01/05124, incorporated herein by reference) a mixed oxide of manganese and zirconium (see WO 99/34904, incorporated herein by reference), Pr2O3 or a combination of any two or more thereof. The ceria stabiliser can be zirconium, lanthanum, aluminium, yttrium, praseodymium or neodymium.
- A preferred TWC for use in the present invention comprises a first PGM, preferably Pt, and the NOx storage component in a first, inner layer and an OSC and a second PGM, preferably Rh, in a second, outer layer.
- This arrangement is advantageous for the following reasons. During stoichiometric running the Rh/OSC component is active for NOx reduction and other reactions while the Pt component is active for oxidation reactions. During oxygen rich conditions the Rh is relatively inactive, the Pt is active for NO, HC and CO oxidation while the NO2 produced is stored in the adsorber as nitrate.
- On subsequent return to lambda=1, the OSC component in the second layer prevents the stored NOx “seeing” reducing gas so that the NOx remains stored as nitrate. The Rh is active for NOx reduction by CO and the Pt is active for oxidation of HC and CO.
- On acceleration the gas mix becomes rich biased, reducing the OSC material so that the stored NOx is released, as the nitrate becomes thermodynamically unstable. The released NOx is then reduced by the Rh layer with the excess reductant,
- According to a further aspect the invention provides a vehicle comprising an engine according to the present invention.
- TWC are generally placed in one or both of two positions in a vehicle according to the intended purpose: the close-coupled position, in which the TWC is disposed as close to the exhaust manifold as possible; and the underfloor position. The reason for placing a TWC in the close-coupled position is to control emissions immediately following cold start, as much of the controlled emissions are emitted during the legislative test cycle immediately following cold-start. By positioning a TWC close to the engine, the catalyst is contacted by hot exhaust gases immediately after key on and accordingly reaches the light-off temperature for CO and HC oxidation sooner than a TWC in the cooler, underfloor location. However, once the exhaust system is up to temperature for efficient three-way conversion, the underfloor catalyst shoulders much of the burden of treating the exhaust gas. Meanwhile the close-coupled TWC is exposed to very high temperatures e.g. up to 1000° C. Indeed one vehicle manufacturer requires testing of close-coupled TWCs for 50 hours at catalyst bed temperatures of at least 970° C. and up to 1010° C. At these sort of temperatures, catalysts can lose activity as materials lose their surface area through sintering events, migration of active species into pores and component interactions. Accordingly, a TWC in the close-coupled position can be expected to lose some of its activity compared with a fresh catalyst. The NOx storage component can also lose NOx storage capacity through this high temperature ageing by loss-of surface area.
- Whilst loss of NOx storage capacity through high temperature ageing, particularly in TWCs located in the close-coupled position, is undesirable in the present invention, the benefit of the invention is still obtained provided that a proportion of NOx storage activity is retained. Accordingly, in an embodiment of the invention, the fresh TWC includes sufficient of the NOx storage component to retain sufficient NOx storage capacity after high temperature ageing, for example in the close-coupled position.
- According to a further aspect, the invention provides An engine control unit for a spark ignition engine comprising an exhaust system comprising a TWC including a NOx storage component, which engine control unit is programmed to control the air-to-fuel ratio of the engine to run at the stoichiometric air-to-fuel ratio during normal running conditions and to run lean of stoichiometry during a defined portion of an engine speed/load map and to determine the amount of NOx contacting the TWC during lean running operation in response to data input from sensor means, thereby to determine the remaining NOx storage capacity of the TWC and to return the air-to-fuel ratio to stoichiometry when the remaining NOx storage capacity is below a pre-determined value, the arrangement being such as to substantially prevent passing more NOx to atmosphere during an engine cycle compared with a spark ignition engine run continuously in stoichiometric mode.
- According to a further aspect, the invention provides A method of treating exhaust gas of a spark ignition engine run at the stoichiometric air-to-fuel ratio during normal running conditions, which engine comprising an exhaust system comprising a TWC including a NOx storage component, which method comprising the steps of controlling the engine air-to-fuel ratio to run lean of stoichiometry during a defined portion of an engine speed/load map and determining the amount of NOx contacting the TWC during lean running operation in response to data input from sensor means, thereby to determine the remaining NOx storage capacity of the TWC and to return the air-to-fuel ratio to stoichiometry when the remaining NOx storage capacity is below a pre-determined value, the arrangement being such as to substantially prevent passing more NOx to atmosphere during an engine cycle compared with a spark ignition engine run continuously in stoichiometric mode.
- In order that the invention may be more fully understood, the following Examples are provided by way of illustration only and with reference to the accompanying drawings, in which:
-
FIG. 1 is a graph showing HC conversion against temperature after ageing of a TWC including a NOx storage component according to the invention, a state-of-the-art TWC and a NOx trap; and -
FIGS. 2, 3 and 4 are graphs showing % conversion of CO, HC and NOx against lambda for a TWC including a NOx storage component according to the invention, a state-of-the-art TWC and a NOx trap formulation respectively. - Three catalyst washcoats were tested. Comparative catalyst A is a state-of-the art Pt/Rh TWC on a thermally stable, high surface area support at a ratio of 5Pt:1Rh and a total precious metal loading of at 60 g ft−3.
- Catalyst B is a TWC including a NOx storage component according to the present invention supported on an identical substrate. It comprised a first, inner layer of a high surface area Al2O3 impregnated with Pt and a NOx storage component, such as BaO, and a second, outer layer of a mixed oxide OSC impregnated with Rh. The ratio of Pt:Rh and the total precious metal loading was the same as for catalyst A.
- Comparative catalyst C is a NOx trap composition comprising a high surface area Al2O3-based mixed oxide support impregnated with Pt, Rh and a NOx storage component. The ratio of Pt:Rh was 6:1 and the total precious metal loading was 70 g ft−3.
- Each washcoat was coated on a 4.66×6 inch (11.9×15.2 cm) ceramic substrate of 400 cells per square inch ((cpsi) 62 cells cm−2) of 0.15 mm wall thickness and the resulting coated substrate was hydrothermally aged at 800° C. for 5 hours under 10% O2/0% H2O balance nitrogen.
- The catalysts were fitted to the exhaust of a four cylinder 2.0 litre Port Fuel Injection bench mounted engine controlled by a Bosch ME7 control system. The catalyst temperature was increased by adjustment of a heat exchanger fitted to the exhaust line before the catalyst. The temperature ramp rate was 14° C./minute.
- The results for the HC light-off (the temperature at which the reaction is catalysed to 50% efficiency) are shown in
FIG. 1 , from which it can be seen that the HC light-off temperature for catalyst B is similar to that of the comparative catalyst A. It can also be seen that the HC light-off temperature of comparative catalyst C is approximately 30° C. higher than comparative catalyst A. - This result shows that the TWC including a NOx storage component (catalyst B) has very similar activity for HC activity compared with a state-of-the-art TWC (comparative catalyst A), despite the presence of the NOx storage component. The NOx trap (comparative catalyst C) performs less well than either catalyst B or comparative catalyst A, despite having a higher Pt loading.
- The same engine as in Example 1 was used to give a catalyst inlet temperature of 450° C. The lambda scans were done using a 10% perturbation (cycling between a
value 10% below lambda=1, i.e. less 0.147 lambda, to a value of 10% above lambda=1 (1.147 lambda)) and at a frequency of 1 Hz. These conditions were chosen to simulate the exhaust gas composition at the inlet to a TWC disposed in an exhaust system including a lambda sensor upstream of the catalyst inlet providing feedback to the engine control unit in order to maintain lambda=1 conditions. - The results are shown in
FIGS. 2, 3 and 4. As can be seen, the NOx trap (comparative catalyst C) is poorer for lambda scan performance (showing poorer conversion), despite having more Pt while the TWC including a NOx storage component (catalyst B) performs similarly to the TWC (comparative catalyst A). - In a bench test cell, a 4 cylinder, 1.8 litre, 1997 model year, Mitsubishi direct injection engine from a vehicle calibrated for the Japanese market was installed with a direct current dynamometer. A catalyst substrate prepared according to Example 1 was fitted in the close-coupled position approximately 30 cm from the engine exhaust manifold. The substrate volume represented of 22% engine swept volume (ESV). Concentrations of NOx, HC, CO2, CO and O2 were measured using a dual bank of MEXA (Motor Exhaust Gas Analyser) 9500 sensors to allow continuous measurement of gas concentrations upstream and downstream of the catalyst The catalyst inlet temperature was measured by thermocouple.
- The engine was operated from one of two sets of maps: one for the homogeneous mode and the other for the lean, stratified mode. Basic maps for ignition and injection timing and duration were generated by firstly logging data from the ECU of a vehicle including the same model of engine as the one used for the bench test and then basing the maps on this information by reverse engineering. In the homogeneous mode, the engine was run at a range of engine speeds and loads and a supplementary map to the basic map was generated for the best emissions of NOx, CO and HC emissions under λ=1 operation. The lean, stratified mode was mapped by matching the torque achieved in homogeneous mode at the same speed and load demand.
- Prior to testing, the engine was thoroughly warmed up in idling condition. In homogeneous mode, the engine was then run so that the inlet temperature to the close-coupled catalyst was 300° C. It was then switched to lean, stratified operation and the EGR valve position was adjusted until the engine-out NOx was 300 ppm. The EGR valve position was recorded and was referred to as the lean set point The engine was switched back to homogeneous mode, and the EGR valve was closed. A rich set point was obtained by increasing the fuel injector pulse width to obtain lambda 0.80. A series of lean/rich cycles were run as follows. In the lean mode, the EGR valve was at the lean set-point position until the NOx efficiency of the system had dropped below 75%. The engine was then switched back to homogeneous mode for 15 seconds, with injector duration at the rich set point. The cycles were repeated five times and the results obtained for each of the cycles were logged. Exhaust systems were fitted to the engine and the protocol above was followed and data collected in the lean, stratified mode at 300° C. catalyst inlet temperature, a typical catalyst inlet temperature for a close-coupled TWC in the exhaust system of a port fuel injection during idling.
- Table 1 shows the NOx storage efficiency with which each of comparative catalysts A and C and catalyst B store NOx, and in particular, how the efficiency with which each catalyst stores 30, 40, 50 and 60 mg of NOx. Thus the NOx trap (comparative catalyst C) stores 60 mg NOx with 97% efficiency, i.e. 97% of the NOx contacting the catalyst is stored, whereas the TWC (comparative catalyst A) stores 60 mg of NOx with 9% efficiency, i.e. for the time it takes to store 60 mg of NOx, the catalyst has slipped 91% of the NOx contacting it.
TABLE 1 NOx storage efficiency Catalyst B Comparative (TWC including Comparative Catalyst C a NOx storage Catalyst A NOx stored (mg) (NOx Trap) component) (TWC) 30 98% 77% 18% 40 98% 73% 16% 50 97% 68% 12% 60 97% 64% 9% - The results of Examples 1, 2 and 3 show that the TWC including a NOx storage component maintains TWC performance despite including a NOx storage component, and that NOx storage capacity is several times higher than a state-of-the-art TWC composition.
Claims (40)
1. A spark ignition engine comprising an exhaust system comprising a catalyst and an engine control unit programmed to control the air-to-fuel ratio of the engine to run at a stoichiometric air-to-fuel ratio during normal running conditions and to run lean of the stoichiometric air-to-fuel ratio during a defined portion of an engine speed/load map, which catalyst comprising a three-way catalyst (TWC) including a NOx storage component, wherein the engine control unit is programmed to determine an amount of NOx contacting the TWC during lean running operation in response to data input from sensor means, thereby a remaining NOx storage capacity of the TWC is determined, and the control unit is programmed to return the air-to-fuel ratio to stoichiometry when the NOx storage capacity is below a pre-determined value.
2. An engine according to claim 1 , wherein the defined portion of the engine speed/load map is engine idle.
3. An engine according to claim 1 , wherein the defined portion of the engine speed/load map comprises driving conditions, wherein a level of NOx emitted by the engine at the driving conditions is up to ten times more than the level of NOx emitted at engine idle conditions.
4. An engine according to claim 1 , further comprising a clock, wherein the data input sensor means includes a predetermined or predicted time elapsed from the start of lean running operation.
5. An engine according to claim 4 , wherein the predicted time is subsequently adjusted in response to data input.
6. An engine according to claim 1 , wherein the sensor means detects a value of airflow over the TWC and the data input includes that detected value.
7. An engine according to claim 1 , wherein the sensor means detects a manifold vacuum value and the data input includes that detected value.
8. An engine according to claim 1 , wherein the sensor means detects an ignition timing value and the data input includes that detected value.
9. An engine according to claim 1 , wherein the sensor means detects an engine speed value and the data input includes that detected value.
10. An engine according to claim 1 , wherein the sensor means detects a throttle position value and the data input includes that detected value.
11. An engine according to claim 1 , wherein the sensor means is a lambda value sensor, and the data input includes the lambda value detected upstream and/or downstream of the TWC.
12. An engine according to claim 1 , wherein the sensor means detects a quantity of fuel injected in the engine and the data input includes that detected quantity.
13. An engine according to claim 1 , further comprising an exhaust gas recirculation (EGR) circuit, wherein the sensor means detects an amount of exhaust gas recirculation by the position of an EGR valve and the data input includes the detected amount of EGR.
14. An engine according to claim 1 , wherein the sensor means detects an engine coolant temperature value and the data input includes that detected value.
15. An engine according to claim 1 , wherein the sensor means comprises a NOx sensor and the data input includes an amount of NOx detected by the NOx sensor upstream and/or downstream of the TWC.
16. An engine according to claim 1 , wherein the engine is a gasoline engine.
17. An engine according to claim 16 , wherein the engine is a port fuel injection engine.
18. An engine according to claim 16 , wherein the engine is a direct injection engine.
19. An engine according to claim 1 , wherein the engine is fuelled by a fuel selected from the group consisting of liquid petroleum gas, natural gas, methanol, and hydrocarbon mixtures including ethanol or hydrogen gas.
20. An engine according to claim 1 , wherein the TWC comprises at least one platinum group metal (PGM).
21. An engine according to claim 20 , wherein the at least one PGM is selected from the group consisting of platinum (Pt), palladium, rhodium (Rh), ruthenium, osmium or iridium and combinations of any two or more thereof.
22. An engine according to claim 1 , wherein the NOx storage component comprises an alkali metal, an alkaline-earth metal or a rare-earth metal or a combination of any two or more thereof.
23. An engine according to claim 22 , wherein the alkali metal is potassium or caesium.
24. An engine according to claim 22 , wherein the alkaline-earth metal is magnesium, calcium, strontium or barium.
25. An engine according to claim 22 , wherein the rare earth metal is a lanthanide group metal.
26. An engine according to claim 1 , wherein the TWC comprises an oxygen storage component (OSC).
27. An engine according to claim 26 , wherein the OSC comprises a component selected from the group consisting of stabilised ceria, perovskites, NiO, MnO2, manganese-based compounds supported on alumina-containing mixed oxide, a mixed oxide of manganese and zirconium, Pr2O3 and combinations of any two or more thereof.
28. An engine according to claim 27 , wherein the ceria stabiliser selected from the group consisting of zirconium, lanthanum, aluminium, yttrium, praseodymium and neodymium.
29. An engine according to claim 1 , wherein the TWC comprises an inner layer comprising a first PGM and the NOx storage component, and an outer layer comprising an OSC and a second PGM.
30. A vehicle including an engine according to claim 1 .
31. A vehicle according to claim 30 , wherein the TWC is in a close-coupled position.
32. A vehicle according to claim 30 , wherein a fresh TWC includes a sufficient amount of the NOx storage component to retain sufficient NOx storage capacity after high temperature ageing.
33. An engine control unit for a spark ignition engine comprising an exhaust system comprising a TWC including a NOx storage component, which engine control unit is programmed to control the air-to-fuel ratio of the engine to run at a stoichiometric air-to-fuel ratio during normal running conditions and to run lean of stoichiometry during a defined portion of an engine speed/load map and to determine an amount of NOx contacting the TWC during lean running operation in response to data input from sensor means, thereby a remaining NOx storage capacity of the TWC is determined, and the control unit is programmed to return the air-to-fuel ratio to stoichiometry when the NOx storage capacity is below a pre-determined value.
34. A method of treating exhaust gas of a spark ignition engine run at the stoichiometric air-to-fuel ratio during normal running conditions, which engine comprising an exhaust system comprising a TWC including a NOx storage component, which method comprising the steps of controlling the engine air-to-fuel ratio to run lean of stoichiometry during a defined portion of an engine speed/load map, determining the amount of NOx contacting the TWC during lean running operation in response to data input from sensor means thereby determining the remaining NOx storage capacity of the TWC, and returning the air-to-fuel ratio to stoichiometry when the remaining NOx storage capacity is below a pre-determined value.
35. (canceled)
36. (canceled)
37. An engine according to claim 29 , wherein the first PGM is platinum.
38. An engine according to claim 29 , wherein the second PGM is rhodium.
39. An engine according to claim 11 , wherein the lambda value sensor is a linear lambda sensor.
40. An engine according to claim 25 , wherein the rare earth metal is lanthanum.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0211971.7A GB0211971D0 (en) | 2002-05-24 | 2002-05-24 | Spark ignition engine including three-way catalyst |
GB0211971.7 | 2002-05-24 | ||
PCT/GB2003/002200 WO2003100228A1 (en) | 2002-05-24 | 2003-05-21 | Spark ignition engine including three-way catalyst with nox storage component |
Publications (1)
Publication Number | Publication Date |
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US20060075740A1 true US20060075740A1 (en) | 2006-04-13 |
Family
ID=9937339
Family Applications (1)
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US10/515,529 Abandoned US20060075740A1 (en) | 2002-05-24 | 2003-05-21 | Spark ignition engine including three-way catalyst with nox storage component |
Country Status (6)
Country | Link |
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US (1) | US20060075740A1 (en) |
EP (1) | EP1507964A1 (en) |
JP (1) | JP4494201B2 (en) |
KR (1) | KR20050013996A (en) |
GB (1) | GB0211971D0 (en) |
WO (1) | WO2003100228A1 (en) |
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US20060051272A1 (en) * | 2004-09-06 | 2006-03-09 | W.C. Heraeus Gmbh | Catalytic converter for 2-cycle engines or small engines |
US20090145117A1 (en) * | 2007-04-25 | 2009-06-11 | Man Nutzfahrzeuge Ag | Exhaust gas aftertreatment system |
US20100051001A1 (en) * | 2008-08-27 | 2010-03-04 | Timothy Webb | Exhaust Gas Recirculation (EGR) System |
DE102010028371A1 (en) | 2010-04-29 | 2011-11-03 | Ford Global Technologies, Llc | Method for controlling exhaust emission of spark ignited Otto engine, involves obtaining modified lambda nominal value by nominal lambda reference value such that dynamic correction terms are added to nominal lambda reference value |
DE102010028373A1 (en) | 2010-04-29 | 2011-11-03 | Ford Global Technologies, Llc | Method for monitoring operating condition of nitrogen oxide-storage catalyst in exhaust gas system of internal combustion engine, involves inducing fully loaded condition of nitrogen oxide-storage catalyst |
US20150198105A1 (en) * | 2014-01-13 | 2015-07-16 | GM Global Technology Operations LLC | Exhaust gas recirculation cooler protection system and method |
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Also Published As
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JP4494201B2 (en) | 2010-06-30 |
WO2003100228A1 (en) | 2003-12-04 |
KR20050013996A (en) | 2005-02-05 |
JP2005534841A (en) | 2005-11-17 |
EP1507964A1 (en) | 2005-02-23 |
GB0211971D0 (en) | 2002-07-03 |
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