EP2073929A1 - Catalyseur pour inhiber la production de no2 - Google Patents
Catalyseur pour inhiber la production de no2Info
- Publication number
- EP2073929A1 EP2073929A1 EP07808305A EP07808305A EP2073929A1 EP 2073929 A1 EP2073929 A1 EP 2073929A1 EP 07808305 A EP07808305 A EP 07808305A EP 07808305 A EP07808305 A EP 07808305A EP 2073929 A1 EP2073929 A1 EP 2073929A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- generation
- inhibiting
- catalyst
- catalyst composition
- module
- 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.)
- Withdrawn
Links
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/024—Multiple impregnation or coating
- B01J37/0246—Coatings comprising a zeolite
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/74—Iron group metals
- B01J23/75—Cobalt
-
- 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]
- B01D53/945—Simultaneously removing carbon monoxide, hydrocarbons or nitrogen oxides making use of three-way catalysts [TWC] or four-way-catalysts [FWC] characterised by a specific catalyst
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
- B01J21/02—Boron or aluminium; Oxides or hydroxides thereof
- B01J21/04—Alumina
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/89—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with noble metals
- B01J23/8933—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with noble metals also combined with metals, or metal oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/8946—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with noble metals also combined with metals, or metal oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with alkali or alkaline earth metals
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J29/00—Catalysts comprising molecular sieves
- B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
- B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
- B01J29/064—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof containing iron group metals, noble metals or copper
- B01J29/072—Iron group metals or copper
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/024—Multiple impregnation or coating
- B01J37/0242—Coating followed by impregnation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2255/00—Catalysts
- B01D2255/10—Noble metals or compounds thereof
- B01D2255/102—Platinum group metals
- B01D2255/1021—Platinum
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2255/00—Catalysts
- B01D2255/10—Noble metals or compounds thereof
- B01D2255/102—Platinum group metals
- B01D2255/1023—Palladium
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2255/00—Catalysts
- B01D2255/20—Metals or compounds thereof
- B01D2255/204—Alkaline earth metals
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2255/00—Catalysts
- B01D2255/20—Metals or compounds thereof
- B01D2255/206—Rare earth metals
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2255/00—Catalysts
- B01D2255/20—Metals or compounds thereof
- B01D2255/207—Transition metals
- B01D2255/20746—Cobalt
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2255/00—Catalysts
- B01D2255/20—Metals or compounds thereof
- B01D2255/209—Other metals
- B01D2255/2092—Aluminium
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2255/00—Catalysts
- B01D2255/40—Mixed oxides
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2255/00—Catalysts
- B01D2255/50—Zeolites
- B01D2255/502—Beta zeolites
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/83—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with rare earths or actinides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J29/00—Catalysts comprising molecular sieves
- B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
- B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
- B01J29/70—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of types characterised by their specific structure not provided for in groups B01J29/08 - B01J29/65
- B01J29/72—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of types characterised by their specific structure not provided for in groups B01J29/08 - B01J29/65 containing iron group metals, noble metals or copper
- B01J29/74—Noble metals
- B01J29/7415—Zeolite Beta
-
- 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 catalyst for inhibiting the generation of NO .
- HC trap catalysts which are used to remove HC discharged when an engine is cold-started, at which time a catalyst does not fulfill its function, by temporarily collecting the HC using a porous material, such as zeolite, and then purifying the HC using an activated catalyst, have also been put to practical use.
- the above exhaust gas purification technologies allow HC and CO to be purified at a constant level.
- NOx which is another cause of photochemical smog, is formed when nitrogen and oxygen in intake air react with each other at high temperatures. Therefore, the amount of NO that is emitted is increased when the engine load is increased due to high speed running. Since NO causes widespread environmental damage, such as smog, acid rain, and the like, NO emission standards have become stricter since ULEV. It has been known that rhodium is very effective in the purification of NO , but the yield of rhodium is low, and the price thereof is very high, compared to platinum or palladium. Accordingly, methods of efficiently purifying NO using a very small amount of rhodium or without using rhodium have been required.
- the amount of exhaust gas that can be treated using a catalyst increases under high-load combustion conditions, and thus the purification performance of NO depends on the degree of contact of exhaust gas and precious metal. For this reason, in addition to the catalyst composition, whether the dispersion state of precious metal is maintained to some degree has been considered.
- diesel engines have high thermal efficiency and air-fuel ratios compared to gasoline engines, and they are thus expected to reduce the emission of CO in Europe.
- vehicles equipped with diesel engines have a problem in that the emission of particulate matter (PM), such as graphite, and NO , required to be purified through reduction, must be decreased.
- PM particulate matter
- Such particulate matter (PM) is solid, and cannot be satisfactorily removed using a conventional flow type catalyst. Therefore, a diesel particulate filter (DPF) is used in order to remove the particulate matter (PM). Since DPF physically collects PM, PM can be removed at high efficiency, but DPF cannot always be operated to thus remove PM, and it is necessary to burn and remove the PM collected on the DPF at a certain point.
- DPF diesel particulate filter
- diesel engine vehicles are equipped with a catalyzed soot filter (CSF), fabricated by catalyzing DPF. That is, diesel engine vehicles are operated in a state in which they are equipped with an oxidation catalyst housing coated with a diesel oxidation catalyst (DOC) and a catalyzed soot filter (CSF) fabricated by catalyzing DPF.
- CSF catalyzed soot filter
- the present inventors have recognized a serious problem in that yellow smog is generated by a diesel engine vehicle in which a DOC and a CSF are serially mounted. As the result of research of the problem, they have found that the yellow smog was derived from NO . That is, they found that NO , which is an oxidation product, was ejected in the form of yellow smog through a tailpipe while NO passes through the DOC and CSF, and they have researched the NO generation mechanism in order to treat NO , thus completing the present invention.
- the present invention relates to the effects of non-precious metal oxides on the conversion of nitrogen oxides, and industrially to a system for inhibiting the generation of NO , visible as yellow smog, the system being equipped with a module for inhibiting the generation of NO , including a refractory carrier coated with a catalyst containing non-precious oxides for inhibiting the generation of NO .
- an object of the present invention is to provide a method of inhibiting the generation of NO .
- Another object of the present invention is to provide a system for inhibiting the generation of NO .
- a further object of the present invention is to provide a method and system for preventing the formation of a visible pollution source by inhibiting the generation of yellow smog.
- the present invention provides a catalyst composition for inhibiting the generation of NO , comprising a basic metal oxide catalyst composition combined with ceria-cobalt oxide, active alumina, and zeolite, wherein the basic metal oxide catalyst composition is supported with a precious metal, such as platinum and/or palladium, and a non-precious metal, such as barium or strontium.
- the present invention provides a module for inhibiting the generation of NO , comprising a refractory carrier coated with the catalyst composition for inhibiting the generation of NO .
- the present invention provides an af- tertreatment system comprising the module for inhibiting the generation of NO , wherein the module is provided immediately behind a DOC and/or a CSF.
- the catalyst composition according to the present invention can be applied to an exhaust gas aftertreatment system as a module for inhibiting the generation of NO , including a refractory carrier supported with the catalyst composition through commonly-used methods.
- the module for inhibiting the generation of NO is disposed at the rear end of a DOC or a CSF, thus inhibiting the generation of NO .
- the module is more preferably disposed at the rear end of the CSF, so that the generation of NO is prevented, with the result that the emission of visible exhaust gas is prevented, thereby contributing to environmental purification.
- FIG. 1 is a graph showing HC conversion rates obtained using non-precious metals, according to the present invention
- FIG. 2 is a graph showing NO/NO conversion rates using non-precious metals, according to the present invention
- FIG. 3 is a graph showing HC conversion rates obtained using the catalyst compositions of Example 1 and Comparative Example 1 according to the present invention.
- FIG. 4 is a graph showing NO/NO conversion rates obtained using the catalyst compositions of Example 1 and Comparative Example 1 according to the present invention.
- active alumina in the present specification means alumina having a high
- the BET surface area includes gamma- alumina, theta-alumina, and alpha- alumina.
- the combination of ceria-cobalt oxide, active alumina, and zeolite is achieved through a process of blending or mixing particles.
- the module for inhibiting the generation of NO according to the present invention includes a refractory carrier coated with the catalyst composition of the present invention.
- the catalyst composition according to the present invention which is a catalytic material for inhibiting the generation of NO , is coated with a mixture of cerium oxide particles impregnated with cobalt, active alumina particles and Fe/zeolite particles, wherein a precious metal, such as platinum and/or palladium, and a non-precious metal, such as barium or strontium, are dispersed in the mixture.
- a precious metal such as platinum and/or palladium
- a non-precious metal such as barium or strontium
- the carrier of the present invention is formed of ceramic materials, such as cordierite, ⁇ -alumina and mullite, and has a monolithic honeycomb structure.
- the ceria-cobalt oxide catalytic material is prepared by drying and calcining a slurry of ceria particles and cobalt salt, and specifically, is prepared by mixing the ceria particles and cobalt salt with an acidifier, such as water, acetic acid, nitric acid, or the like, and then milling the mixture to a desired particle size.
- the basic metal oxide catalyst composition composed of ceria-cobalt oxide, active alumina, and Fe/zeolite, is a constituent of the catalytic material of the present invention, and serves as a support for other constituents thereof, including a precious metal, such as Pt or Pd, and a non- precious metal, such as Ba or Sr.
- the basic metal oxide catalyst composition is applied on a carrier, and the carrier is impregnated with a precious metal compound solution and a non-precious metal compound solution, dried, and then calcined, thus preparing a catalyst composition for inhibiting the generation of NO .
- the fixation of the carrier may be conducted by calcination, H2S treatment, and other commonly-known methods.
- the fixation of the carrier is conducted in order to impart insolubility to a catalyst.
- platinum (Pt) compound potassium platinum chloride, ammonium platinum thiocyanate, amine-solubilized platinum hydroxide, chloroplatinic acid, or the like may be used.
- palladium (Pd) compound palladium nitrate, palladium chloride, or the like, which are commonly used in this field, may be used.
- barium (Ba) compound barium hydroxide, barium nitrate, or barium acetate may be used, and, as the strontium (Sr) compound, strontium hyd roxide, strontium nitrate, or strontium acetate may be used.
- Step A 205.1 g of Y-alumina powder was mixed with acetic acid having a concentration of about 1.5% based on the weight of the Y-alumina powder to form a mixture, the mixture was sufficiently mixed with 300 g of H O to form slurry, and then the slurry was ball-milled such that 90% by weight of the particles in the slurry had a particle size of 8 ⁇ 10 D.
- the slurry formed in this step was referred to as slurry A.
- Step B The preparation of ceria-cobalt oxide: 981.1 g of cerium oxide was sufficiently mixed with 149.8 g of cobalt nitrate and about 170 g of H O to form slurry. Subsequently, the slurry was dried at a temperature of 12O 0 C for about 2 hours, and then calcined at a temperature of 500 0 C for about 2 hours, thus preparing ceria-cobalt oxide.
- Step C The slurry A was mixed with 101.5 g of the ceria-cobalt oxide, and was then ball-milled such that 90% by weight of the particles in the slurry A had a particle size of 6 ⁇ 8 D to form slurry B. Subsequently, the slurry B was mixed with 444 g of Fe/ ⁇ -zeolite, and was then dispersed for about 30 minutes to form slurry C.
- Step D A cordierite honeycomb core was coated with the slurry C, dried at a temperature of 15O 0 C for about 20 minutes, and then calcined at a temperature of 500 0 C for about 5 hours.
- Step E The basic metal oxide catalyst composition applied on the cordierite honeycomb core was impregnated with 0.2 g of Pt and 5 g of Ba using chloroplatinic acid and barium compounds through commonly-known methods, thus completing a catalyst composition for inhibiting the generation of NO according to the present invention.
- Example 1 Although Y-alumina was used as an active alumina, theta-alumina and alpha- alumina may be each independently used as the active alumina, and combinations thereof may also be used as the active alumina. As described above, in addition to cordierite, ⁇ -alumina or mullite may be used as the carrier. Further, the catalyst composition according to the present invention may be completed by impregnating the catalyst composition with Pd instead of Pt or impregnating it with Sr instead of Ba. Further, in step E, even when the amount of Pt is adjusted to 1.6 or 3.2 gll, or when the amount of Ba is adjusted to 2 or 20 gll, the effect of inhibiting the generation of NO is not reduced.
- the Pt/Ba/ceria-cobalt oxide/T-alumina/zeolite catalyst was produced as in Example 1, except the process of impregnating the basic metal oxide catalyst composition with Ba.
- NOx consists of NO and NO , and the NO conversion rate means the rate at which
- NO was converted into molecules other than NO and NO , that is, the rate of at which x 2
- Example 1 based on the tests, and then measured the HC conversion rate and the NO/NO conversion rate using the catalysts, and the results thereof are shown in FIGS. 3 and 4. From FIGS. 3 and 4, it can be seen that the catalyst of Example 1 exhibits the effect of considerably inhibiting NO formation (see FIG. 4) while not changing the HC conversion rate (see FIG. 3), and thus the catalyst composition according to the present invention inhibits NO formation, thereby reducing the generation of yellow smog.
Abstract
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020060097585A KR100809661B1 (ko) | 2006-10-04 | 2006-10-04 | No2 생성 억제 촉매 |
PCT/KR2007/004515 WO2008041801A1 (fr) | 2006-10-04 | 2007-09-18 | Catalyseur pour inhiber la production de no2 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP2073929A1 true EP2073929A1 (fr) | 2009-07-01 |
EP2073929A4 EP2073929A4 (fr) | 2011-10-05 |
Family
ID=39268639
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP07808305A Withdrawn EP2073929A4 (fr) | 2006-10-04 | 2007-09-18 | Catalyseur pour inhiber la production de no2 |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP2073929A4 (fr) |
KR (1) | KR100809661B1 (fr) |
WO (1) | WO2008041801A1 (fr) |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0507590A1 (fr) * | 1991-04-05 | 1992-10-07 | Nippon Shokubai Co., Ltd. | Catalyseur pour la purification des effluents gazeux |
US5736482A (en) * | 1995-02-03 | 1998-04-07 | Institut Francais Du Petrole | Catalysts for reducing nitrogen oxides to molecular nitrogen in a superstoichiometric medium of oxidizing compounds, process for preparation, and uses |
EP0931590A1 (fr) * | 1998-01-27 | 1999-07-28 | Mazda Motor Corporation | Catalysateur pour la purification des effluents gazeux et méthode pour le préparer |
US20010049337A1 (en) * | 1995-04-28 | 2001-12-06 | Mazda Motor Corporation | Burned gas purifying catalyst |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0624393B1 (fr) * | 1993-05-10 | 2001-08-16 | Sakai Chemical Industry Co., Ltd., | Catalyseur pour la réduction catalytique d'oxydes d'azote |
KR200150138Y1 (en) | 1994-02-23 | 1999-07-01 | Cataler Ind Co | Catalyst for purifying exhaust gases |
US5814577A (en) | 1995-10-09 | 1998-09-29 | Samsung Electro-Mechanics Co., Ltd. | Catalyst and fabrication method of same for purifying exhaust gases of automobile |
KR100279938B1 (ko) | 1998-09-11 | 2001-03-02 | 임의신 | No 산화촉매 조성물 |
US6756338B2 (en) * | 2001-09-19 | 2004-06-29 | Johnson Matthey Public Limited Company | Lean NOx trap/conversion catalyst |
US7030055B2 (en) * | 2003-08-18 | 2006-04-18 | W.R. Grace & Co.-Conn. | NOx reduction compositions for use in FCC processes |
KR20050118762A (ko) * | 2004-06-15 | 2005-12-20 | 현대자동차주식회사 | 디젤 개질기를 이용한 자동차 배기가스 정화 시스템 |
-
2006
- 2006-10-04 KR KR1020060097585A patent/KR100809661B1/ko active IP Right Grant
-
2007
- 2007-09-18 EP EP07808305A patent/EP2073929A4/fr not_active Withdrawn
- 2007-09-18 WO PCT/KR2007/004515 patent/WO2008041801A1/fr active Application Filing
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0507590A1 (fr) * | 1991-04-05 | 1992-10-07 | Nippon Shokubai Co., Ltd. | Catalyseur pour la purification des effluents gazeux |
US5736482A (en) * | 1995-02-03 | 1998-04-07 | Institut Francais Du Petrole | Catalysts for reducing nitrogen oxides to molecular nitrogen in a superstoichiometric medium of oxidizing compounds, process for preparation, and uses |
US20010049337A1 (en) * | 1995-04-28 | 2001-12-06 | Mazda Motor Corporation | Burned gas purifying catalyst |
EP0931590A1 (fr) * | 1998-01-27 | 1999-07-28 | Mazda Motor Corporation | Catalysateur pour la purification des effluents gazeux et méthode pour le préparer |
Non-Patent Citations (1)
Title |
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See also references of WO2008041801A1 * |
Also Published As
Publication number | Publication date |
---|---|
KR100809661B1 (ko) | 2008-03-05 |
EP2073929A4 (fr) | 2011-10-05 |
WO2008041801A1 (fr) | 2008-04-10 |
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