WO2010129490A2 - Improved lean hc conversion of twc for lean burn gasoline engines - Google Patents
Improved lean hc conversion of twc for lean burn gasoline engines Download PDFInfo
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- WO2010129490A2 WO2010129490A2 PCT/US2010/033457 US2010033457W WO2010129490A2 WO 2010129490 A2 WO2010129490 A2 WO 2010129490A2 US 2010033457 W US2010033457 W US 2010033457W WO 2010129490 A2 WO2010129490 A2 WO 2010129490A2
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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
- B01J23/38—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
- B01J23/46—Ruthenium, rhodium, osmium or iridium
- B01J23/464—Rhodium
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- 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
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- 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]
- B01D53/9454—Simultaneously removing carbon monoxide, hydrocarbons or nitrogen oxides making use of three-way catalysts [TWC] or four-way-catalysts [FWC] characterised by a specific device
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
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- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/002—Mixed oxides other than spinels, e.g. perovskite
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- 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
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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
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/56—Platinum group metals
- B01J23/63—Platinum group metals with rare earths or actinides
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- 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
- B01J37/0244—Coatings comprising several layers
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- 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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- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
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- B01D2255/00—Catalysts
- B01D2255/10—Noble metals or compounds thereof
- B01D2255/102—Platinum group metals
- B01D2255/1023—Palladium
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- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
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- B01D2255/10—Noble metals or compounds thereof
- B01D2255/102—Platinum group metals
- B01D2255/1025—Rhodium
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B01D—SEPARATION
- B01D2255/00—Catalysts
- B01D2255/20—Metals or compounds thereof
- B01D2255/204—Alkaline earth metals
- B01D2255/2042—Barium
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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
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- B01D—SEPARATION
- B01D2255/00—Catalysts
- B01D2255/20—Metals or compounds thereof
- B01D2255/207—Transition metals
- B01D2255/20715—Zirconium
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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
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- B01D2255/40—Mixed oxides
- B01D2255/407—Zr-Ce mixed oxides
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2255/00—Catalysts
- B01D2255/90—Physical characteristics of catalysts
- B01D2255/902—Multilayered catalyst
- B01D2255/9025—Three layers
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2258/00—Sources of waste gases
- B01D2258/01—Engine exhaust gases
- B01D2258/014—Stoichiometric gasoline engines
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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
- B01J2523/00—Constitutive chemical elements of heterogeneous catalysts
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- 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
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- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S502/00—Catalyst, solid sorbent, or support therefor: product or process of making
- Y10S502/52712—Plural layers on a support, each layer having a distinct function
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- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S502/00—Catalyst, solid sorbent, or support therefor: product or process of making
- Y10S502/52712—Plural layers on a support, each layer having a distinct function
- Y10S502/52713—More than two overlapping layers
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- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S502/00—Catalyst, solid sorbent, or support therefor: product or process of making
- Y10S502/52718—Monolith with specified gas flow patterns, e.g. turbulent flow monolith
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- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S502/00—Catalyst, solid sorbent, or support therefor: product or process of making
- Y10S502/52719—Monolith with specified shape or dimension of cell opening, e.g. honeycomb, rings
Definitions
- This invention relates to layered catalysts used to treat exhaust gas steams, in particular exhaust gas streams containing hydrocarbons, carbon monoxide, and oxides of nitrogen.
- TWC catalysts have utility in a number of fields including the treatment of exhaust gas streams from internal combustion engines, such as automo- bile, truck and other gasoline-fueled engines. Emission standards for unbumed hydrocarbons, carbon monoxide and nitrogen oxide contaminants have been set by various governments and must be met by older as well as new vehicles. In order to meet such standards, catalytic converters containing a TWC catalyst are located in the exhaust gas line of internal combustion engines. Such catalysts promote the oxidation by oxy- gen in the exhaust gas stream of unburned hydrocarbons and carbon monoxide as well as the reduction of nitrogen oxides to nitrogen.
- the support is carried on a suitable carrier or substrate such as a monolithic carrier comprising a refractory ceramic or metal honeycomb structure, or refractory particles such as spheres or short, extruded segments of a suitable refractory material.
- TWC catalysts can be manufactured in many ways. US 6,478,874, for example, sets forth a system for catalytic coating of a substrate.
- TWC catalysts having two layers with precious metals.
- US 6,764,665 discloses a TWC catalyst having three layers, two of which have precious metals.
- WO 2008/024708 discloses a layered, three-way conversion catalyst having the capability of simultaneously catalyzing the oxidation of hydrocarbons and carbon monoxide and the reduction of nitrogen oxides.
- the catalyst comprises three layers in conjunction with a carrier: a first layer deposited on the carrier and comprising palladium deposited on a refractory metal oxide and an oxygen storage component; a second layer deposited on the first layer and comprising rhodium deposited on a refractory metal oxide and an oxygen storage component; and a third layer deposited on the second layer and comprising palladium deposited on a refractory metal oxide.
- WO 2008/097702 relates to a multilayered, three-way conversion catalyst having the capability of simultaneously catalyzing the oxidation of hydrocarbons and carbon monoxide and the reduction of nitrogen oxides.
- a catalytic material of at least four layers in conjunction with a carrier, where each of the layers includes a support, at least three layers comprise a precious metal component, and at least one layer comprises an oxygen storage component (OSC).
- the catalytic material can further comprise a fifth layer, where at least four layers comprise a precious metal component, at least one layer comprises an oxygen storage component, and at least one layer is substantially free of an oxygen storage component.
- Multilayered catalysts are widely used in TWC.
- vehicles require catalysts having the same general overall conversion functionalities, but different vehicle platforms dictate the configurations on the catalyst of individual functions.
- the engine control of a particular vehicle dictates whether, for example, HC or NOx conver- sion will be the determining factor to meet regulation targets.
- These critical factors lead to catalysts designed with different outer-most layer favoring either HC or NOx conversion.
- Multilayered catalysts are formed by deposition of washcoats onto the carriers or substrates.
- deposition of washcoats along a length of the carrier or substrate is limited. For example, sometimes a single pass of a washcoat covers less than 100% of the length of the catalyst, for example, only about 80-90%.
- the present invention relates to a catalyst composition
- a catalyst composition comprising: a carrier substrate; a layer (i) coated on said carrier substrate comprising at least one precious group metal; a layer (ii) comprising Rh; - a layer (iii) comprising Pd and/or Pt and being substantially free of Ce, Ba and Rh,
- the layer (iii) has a lower weight than the layer (i) or the layer (ii),
- the present invention relates to a catalyst composition as disclosed above, wherein the layer (ii) is coated over the layer (i) and the layer (iii) is coated over the layer (ii).
- the present invention relates to a catalyst composi- tion as disclosed above, wherein the layer (iii) is coated over the layer (i) and the layer (ii) is coated over the layer (iii).
- the present invention relates to a method for treating an exhaust gas stream, the method comprising the steps of: (i) providing a catalyst composition comprising: a carrier substrate; a layer (i) coated on said carrier substrate comprising at least one precious group metal; a layer (ii) comprising Rh; - a layer (iii) comprising Pd and/or Pt and being substantially free of Ce,
- the layer (iii) has a lower weight than the layer (i) or the layer (ii); (ii) contacting said exhaust gas stream with said catalyst composition for the treatment of exhaust gas emissions.
- the present invention relates to a layered catalyst composition of the type generally referred to as a three-way conversion (TWC) catalyst.
- TWC catalysts are poly- functional in that they have the capability of substantially simultaneously catalyzing the oxidation of hydrocarbons and carbon monoxide and the reduction of nitrogen oxides.
- the relative layers of the catalyst composite and the specific composition of each such layer provide a stable, economical system. This enables the enhanced oxidation of hydrocarbons and carbon monoxide as well as effective conversion of nitrogen oxide compounds to nitrogen,
- the present invention relates to a catalyst composition
- a catalyst composition comprising:
- a carrier substrate comprising at least one precious group metal; a layer (ii) comprising Rh; a layer (iii) comprising Pd and/or Pt and being substantially free of Ce, Ba and Rh,
- the layer (iii) has a lower weight than the layer (i) or the layer (ii).
- the catalyst composition comprises at least a carrier substrate and three layers (i), (ii), and (iii).
- Ce and Ba may be present at a level of less than or equal to approximately 0.1 %.
- Rh may be present at a level of less than or equal to approximately 100 ppm.
- layer (i) is coated over the carrier substrate.
- Layer (ii) may be coated over layer (i). in this case, layer (iii) is coated over layer (ii).
- layer (iii) may be coated over layer (i). In this case, layer (ii) is coated over layer (iii).
- the present invention relates to a catalyst composition as disclosed above, wherein the layer (ii) is coated over the layer (i) and the layer (iii) is coated over the layer (ii).
- the present invention relates to a catalyst composition as disclosed above, wherein the layer (iii) is coated over the layer (i) and the layer (ii) is coated over the layer (iii).
- the catalyst composition according to the present invention can also comprise further layers. These layers can be arranged in any order and can also be intermediate layers between any of the layers or the carrier substrate disclosed above. According to the present invention additional layers may comprise any suitable material, for example a porous material, e.g. a base metal oxide and transition metal oxide, or a microporous material.
- the catalyst composition according to the present invention oniy comprises the carrier substrate, and layers (i), (ii), and (iii).
- the layer (iii) has a lower weight than the layer (i) or the layer (ii).
- the weight of layer (iii) is preferably only about 90% or less of the weight of the layer (i), more preferably about 85% or less of the weight of the layer (i), in particular only about 80% or less of the weight of the iayer (i), for example 80% to 50% of the weight of the layer (i).
- the present invention relates to a catalyst composition as disclosed above, wherein the weight of the layer (iii) is about 80% or less of the weight of the layer (i).
- the catalyst composition of the present invention comprises a carrier substrate.
- any suitable carrier substrate known to the person skilled in the art can be used in the context of the present invention.
- the carrier substrate may be any of those ma- terials typically used for preparing TWC catalysts and will typically comprise a metal or ceramic honeycomb structure.
- Any suitable carrier may be employed, such as a monolithic carrier of the type having a plurality of fine, parallel gas flow passages extending therethrough from an inlet or an outlet face of the carrier, such that passages are open to fluid flow therethrough.
- the passages which are essentially straight paths from their fluid inlet to their fluid outlet, are defined by walls on which the catalytic material is coated as a "washcoat" so that the gases flowing through the passages contact the catalytic material.
- washcoat has its usual meaning in the art of a thin, adherent coating of a catalytic or other material applied to a substrate carrier material which is sufficiently porous to permit the passage there through of the gas stream being treated.
- the flow passages of the monolithic carrier are thin- walled channels which can be of any suitable cross-sectional shape and size such as trapezoidal, rectangular, square, sinusoidal, hexagonal, oval, circular, etc.
- Such structures may contain from about 60 to about 1200 or more gas inlet openings (i.e., "cells”) per square inch of cross section.
- the carrier substrate can also be a wail-flow filter substrate, where the channels are alternately blocked, allowing a gaseous stream entering the channels from one direction (inlet direction), to flow through the channel walls and exit from the channels from the other direction (outlet direction).
- a dual oxidation catalyst composition can be coated on the wall-flow filter. If such a carrier is utilized, the resulting system will be able to remove particulate matters along with gaseous pollutants.
- the wall-flow filter carrier can be made from materials commonly known in the art, such as cordierite or silicon carbide.
- the ceramic carrier may be made of any suitable refractory material, e.g., cordierite, cordierite-alumina, in particular cordierite-alpha-alumina, silicon nitride, zircon mullite, spodumene, alumina-silica magnesia, zircon silicate, sill ⁇ manite, magnesium silicates, zircon, petalite, alumina, in particular alpha-alumina, aluminosilicates and the like.
- suitable refractory material e.g., cordierite, cordierite-alumina, in particular cordierite-alpha-alumina, silicon nitride, zircon mullite, spodumene, alumina-silica magnesia, zircon silicate, sill ⁇ manite, magnesium silicates, zircon, petalite, alumina, in particular alpha-alumina, aluminosilicates and the like.
- the carriers useful for the catalyst compositions of embodiments of the present invention may also be metallic in nature and be composed of one or more metals or metal alloys.
- the metallic carriers may be employed in various shapes such as corrugated sheet or monolithic form.
- Exemplary metallic supports include the heat resistant metals and metal alloys such as titanium and stainless steel as well as other alloys in which iron is a substantial or major component.
- Such alloys may contain one or more of nickel, chromium and/or aluminum, and the total amount of these metals may comprise at least 15 wt. % of the alloy, e.g., 10-25 wt. % of chromium, 3-8 wt. % of aluminum and up to 20 wt. % of nickel.
- the alloys may also contain small or trace amounts of one or more other metals such as manganese, copper, vanadium, titanium and the like.
- the surface or the metal carriers may be oxidized at high temperatures, e.g., 1000 0 C and higher, to improve the corrosion resistance of the alloy by forming an oxide layer on the surface the carrier. Such high temperature-induced oxidation may enhance the adherence of the refractory metal oxide support and catalytically- promoting metal components to the carrier.
- the catalyst composition may be deposited on an open cell foam substrate.
- substrates are well known in the art, and are typically formed of refractory ceramic or metallic materials.
- the catalyst composition according to the present invention further comprises layer (i) comprising at least one precious group metal.
- layer (i) comprises two or more precious group metals.
- the precious group metal is at least one metal selected from Pt, Pd, Rh, Au, and Ir, in particular at least one metal selected from Pt and Pd. More preferably, the layer (i) comprises Pt and Pd.
- the present invention relates to a cataiyst composition as disclosed above, wherein the precious group metal is at least one metal selected from Pt, Pd, Rh, Au, and Ir.
- the present invention relates to a catalyst composition as disclosed above, wherein the precious group metaf is Pt and/or Pd.
- the layer (i) may contain Pd and/or Pt in a suitable range. Suitable ranges for Pt are between 0 to 100 g/ft 3 , preferably, layer (i) contains no Pt. In the case Pd is present suitable ranges are between 1 and 20Og /ft 3 preferably between about 30 to about 100 g/ft 3 .
- the layer (i) may comprise the precious group metal as such.
- the precious group metal may also be dispersed on a suitable support material.
- any suitable support material in particular any porous support material may be used. Preferred support materials, in particular preferred porous support materials are disclosed below.
- Layer (i) may comprise further components.
- Layer (i) may for example comprise further components selected from the group of alumina, e.g. alumina doped with lanthanum, barium, zirconium, ceria, praseodymium or other rare earth elements to a level of 0.1 to 20%.
- the alumina may comprise up to four different dopands in one alumina.
- Further components in layer (i) may be ceria or ceria zirconia mixed oxides doped or non doped. Suitable dopands are lanthanum, neodymium, yttrium or rare earth elements in a level from 0.1 to 20 %. Up to four different dopands can be present in one Ceria or ceria zirconia mixture.
- layer (i) may contain ZrO2 doped or non doped like the above materials, barium oxide or carbonate.
- Suitable amounts for the additional components are for example in the range of 0.5 - 1.5 g/in 3 alumina, 0.1- 1 g/in 3 ceria or ceria/zirconia, 0.1-1g/in 3 , and 0.1-1g/in 3 barium- oxide or barium carbonate.
- the catalyst composition according to the present invention also comprises layer (ii) comprising Rh.
- Layer (ii) may comprise further components. However, according to the present invention, layer (ii) is preferably substantially free of Pd and/or Pt, particularly preferred substantially free of Pd and Pt.
- the present invention relates to a catalyst composition as disclosed above, wherein the layer (ii) is substantially free of Pd and/or Pt.
- Layer (ii) may comprise further components.
- Layer (ii) may for example comprise components which are mentioned above as suitable further components for layer (i).
- the catalyst composition according to the present invention further comprises layer (iii) comprising Pd and/or Pt and being substantially free of Ce, Ba and Rh.
- Layer (iii) may comprise Pd and/or Pt and preferably comprises Pd and Pt. Therefore, according to a further embodiment, the present invention relates to a catalyst composition as disclosed above, wherein the layer (iii) comprises Pd and Pt.
- Layer (iii) may comprise Pd and Pt in a ratio in a range of from 0:5 to 5:1 , preferably in a ratio in a range of from 1 :4 to 4:2, in particular in a ratio in a range of 1 :1.
- the present invention therefore relates to a catalyst composition as disclosed above, wherein the ratio of Pd and Pt in the layer (iii) is in the range of from 0:5 to 5:1. Suitable amount of Pt are in the range from 1g/ft 3 to 50 g/ft 3 . Pd is added to yield the desired ratio of Pt to Pd.
- the layer (iii) may comprise Pd and/or Pt as such.
- Pd and/or Pt may also be dispersed on a suitable support material.
- any suitable support material in particular any porous support material may be used.
- Preferred support materials, in particular preferred porous support materials are disclosed below.
- Layer (iii) may also comprise further components.
- Layer (iii) may for example comprise further components selected from the group of alumina doped with lanthanum, zirconium, praseodymium or other rare earth elements other than ceria to a level of 0.1 to 20%. Up to four different dopands can be present in one alumina.
- the catalyst composition according to the present invention may suitably contain up to 3.0 wt-% of barium oxide based on the total weight of the layers.
- any of the layers (i), (ii), and/or (iii) additionally comprises a porous support material.
- Suitable porous support materials are known to the person skilled in the art.
- the porous support material is preferably a base metal oxide and / or transition metal oxide which are selected from the group including compounds of silica, alumina, zirconia, titania and mixtures thereof.
- the porous support material is a material with a porosity between 0.2 to 1.2 mL/g, preferable between about 0.2 and about 0.8 m L/g.
- the porous support material preferably has a BET surface area between 30 and 300 m 2 /g, more preferably between about 50 and about 200 nrVg.
- the present invention relates to a catalyst composition as disclosed above, wherein the layer (i) or the layer (ii) or the layer (iii) or the layers (i) and (ii) or the layers (i) and (iii) or the layers (ii) and (iii) or the layers (i), (ii) and (iii) additionaily comprises a porous support material.
- a suitable support material according to one or more embodiments is a refractory oxide support.
- references to a "support” in a catalyst layer refers to a material onto or into which pre- cious metals, stabilizers, promoters, binders, and the like are dispersed or impregnated, respectively.
- a support can be activated and/or stabilized as desired. Examples of supports include, but are not limited to, high surface area refractory metal oxides, composites containing oxygen storage components, and molecular sieves.
- the support of each layer independently comprises a compound that is activated, stabilized, or both selected from the group consisting of, but not limited to, alumina, silica, silica-alumina, alumino-siltcates, alumina- zirconia, lanthana-alumina, ianthana-zirconia-alumina, baria-alumina, baria lanthana-alumina, alumina-chromia, and alumina-ceria.
- the support may comprise any suitable materials, for example, a metal oxide comprising gamma-alumina or promoter-stabilized gamma- alumina having a specific surface area of about 50 to 300 m 2 /g.
- the alumina present in any of the layers comprises zirconia- and lanthana- stabilized gamma-alumina in a loading of about 0,2 to about 2.0 g/in 3 .
- a suitable alumina is about 0.1- 15% lanthana and about 2-25%, and specifically 8-20%, zirconia-stabilized gamma alumina.
- the alumina com- prises gamma alumina stabilized by barium oxide, neodymia, lanthana and combinations thereof.
- An example of a suitable alumina is about 4% barium oxide and about 4% lanthana stabilized alumina.
- the present invention relates to a catalyst composition as disclosed above, wherein the porous support material is selected from base metal oxides and transition metal oxides.
- an exhaust gas treatment system or article containing a catalytic member or catalytic converter comprising a substrate on which is coated one or more washcoat layers, each containing one or more catalysts for the abatement of poliutants, especially NOx, HC, and CO.
- washcoat has its usual meaning in the art of a thin, adherent coating of a catalytic or other material applied to a substrate carrier material, such as a honeycomb-type carrier member, which is sufficiently porous to permit the passage there through of the gas stream being treated.
- the coating process can be manipulated such that the third layer is applied over only a fraction of the second layer.
- the third layer can be applied or coated to the upstream portion of the substrate, thereby creating an upstream poison capture zone.
- upstream and downstream refer to relative directions according to the flow of an engine exhaust gas stream.
- the third layer was introduced again to enhance HC/CO/NOX activity this upstream zone where turbulent mass transfer occurs.
- the catalyst composition of the present invention can be prepared by any suitable method.
- each layer of the oxidation catalyst of the present invention can be applied to the substrate surfaces by any known means in the art.
- the catalyst composition can be applied by spray coating, powder coating, or brushing or dipping a surface into the catalyst composition.
- the individual layers can be applied by any suitable method and after one layer has been applied, preferably a drying step or a drying and a calcination step are applied before the next layer is applied.
- each layer can be applied on the substrate or a layer below completely or in form of a zone covering the substrate or layer below in an amount of about 10 to 100% of the length of the substrate or layer below.
- the remaining uncovered part of the substrate or layer can be covered with another layer as disclosed above.
- a zone covers preferably 30 to 70% of the length of the substrate or layer below.
- the catalyst composition can be prepared in layers on a monolithic carrier.
- finely divided particles of a high surface area refractory metal oxide such as gamma alumina are slurried in an appropriate vehicle, e.g., water.
- the carrier may then be dipped one or more times in such slurry or the slurry may be coated on the carrier such that there will be deposited on the carrier the desired loading of the metal oxide, e.g., about 0.5 to about 2.5 g/in 3 .
- the coated carrier is cal- cined by heating, e.g., at 500-600 0 C for about 1 to about 3 hours.
- Water-soluble compounds or water-dispersible compounds or complexes of the metal component may be used as long as the liquid medium used to impregnate or deposit the metal component onto the refractory metal oxide support particles does not adversely react with the metal or its compound or its complex or other components which may be present in the catalyst composition and is capable of being removed from the metal component by volatilization or decomposition upon heating and/or application of a vacuum. In some cases, the completion of removal of the liquid may not take place until the catalyst is placed into use and subjected to the high temperatures encountered during operation. Generally, both from the point of view of economics and environmental aspects, aque- ous solutions of soluble compounds or complexes of the precious metals are utilized.
- suitable compounds are palladium nitrate or rhodium nitrate.
- such compounds are converted into a catalytically active form of the metal or a compound thereof.
- a suitable method of preparing any layer of the layered catalyst composite of the invention is to prepare a mixture of a solution of a desired precious metal compound (e.g., palladium compound or palladium and platinum compounds) and at least one finely divided, high surface area, refractory metal oxide support, e.g., gamma alumina, which is sufficiently dry to absorb substantially all of the solution to form a wet solid which later combined with water to form a coatable slurry,
- the slurry is acidic, having a pH of about 2 to less than about 7. The pH of the slurry may be lowered by the addition of a minor amount of an inorganic or an organic acid to the slurry.
- Inorganic acids include, but are not limited to, nitric acid.
- Organic acids include, but are not limited to, as acetic acid or polyacids, specifically difunctionat acids, more specifically dicarboxylic acids.
- Dicarboxy ⁇ c acids include, but are not limited to oxalic, malonic, succinic, glutaric, adipic, maleic, fumaric, phthalic, tartaric, and the like. Combinations of both organic and inorganic acids can be considered when amounts of each are desired.
- the slurry is thereafter comminuted to result in substantially all of the solids having particle sizes of less than about 50 microns, preferably between about 0.1-15 microns, in an average diameter. The comminution may be accomplished in a ball mill or other similar equipment, and the solids content of the slurry may be, e.g., about 15-60 wt. %, more particularly about 25-40 wt. %.
- Additional layers i.e., the second, third, fourth, and fifth layers may be prepared and deposited upon the first layer in the same manner as described above for deposition of the first layer upon the carrier.
- the present invention relates to a method for treating an exhaust gas stream, the method comprising the steps of: (i) providing a catalyst composition comprising: a carrier substrate; a layer (i) coated on said carrier substrate comprising at (east one precious group metal; a layer (ii) comprising Rh; a layer (iii) comprising Pd and/or Pt and being substantially free of Ce, Ba and Rh, wherein the layer (iii) has a lower weight than the layer (i) or the layer (ii);
- the present invention relates to a method for treat- ing an exhaust gas stream as disclosed above, wherein in the catalyst composition the layer (ii) is coated over the layer (i) and the layer (iii) is coated over the layer (ii).
- the present invention relates to a method for treating an exhaust gas stream as disclosed above, wherein in the catalyst composition the layer (iii) is coated over the layer (i) and the layer (ii) is coated over the layer (iii).
- catalyst composition as disclosed above including preferred embodiments can be used for the method for treating an exhaust gas stream according to the present invention.
- a further aspect of the present invention includes a method comprising locating in an exhaust system a multi-layered catalyst composition having a catalytic material on a carrier, the catalyst composition comprising; a carrier substrate; a layer (i) coated on said carrier substrate comprising at least one precious group metal; a layer (ii) comprising Rh; a layer (iii) comprising Pd and/or Pt and being substantially free of Ce, Ba and Rh, wherein the layer (iii) has a lower weight than the layer (i) or the layer (ii).
- a catalyst composition comprising:
- a carrier substrate comprising at least one precious group metal; a layer (ii) comprising Rh; a layer (iii) comprising Pd and/or Pt and being substantially free of Ce, Ba and Rh 1
- the iayer (iii) has a lower weight than the layer (i) or the layer (ii).
- porous support material is selected from base metal oxides and transition metal oxides.
- a method for treating an exhaust gas stream comprising the steps of:
- a catalyst composition comprising: a carrier substrate; a layer (i) coated on said carrier substrate comprising at least one precious group metal; a layer (ii) comprising Rh; a layer (iii) comprising Pd and/or Pt and being substantially free of Ce, Ba and Rh, wherein the layer (iii) has a lower weight than the layer (i) or the layer (ii);
- a composite having a catalytic material was prepared using three layers: an inner layer, a middle layer, and an outer layer.
- the composition is generally referred to as UC/Pd/Pd (where UC refers to "undercoat”).
- the layered catalyst composite contained platinum, palladium and rhodium with a total precious metal loading of 105 g/ft 3 and with a Pt/Pd/Rh ratio of 8/95/2.
- the substrate had a volume of 51.2 in 3 (0.84 L), a cell density of 600 cells per square inch, and a wall thickness of approximately 100 ⁇ m.
- the catalytic material as a whole had an OSC content of 29% by weight.
- the inner layer and the middle layer have equal thickness while the outer has only 60 % of the thickness of the other layers.
- the top layer contains platinum but no ceria or baria and no Rh.
- the middle layer contains no Pd but Rh and the bottom layer contains Pd only.
- the layers were prepared as follows:
- the components present in the inner layer were high surface area gamma alumina doped with 4% of lanthanum, a ceria-zirconia composite with 45% ceria by weight, zirconium oxide, barium oxide and a binder, at concentrations of approximately 67%, 18%, 3%, 6% and 3%, respectively, based on the calcined weight of the catalyst.
- the total loading of the inner layer was 1.649 g/in 3 .
- the zirconium oxide was introduced as an acetate colloidal solution and the barium oxide as barium acetate solution.
- Palladium in the form of a Palladium nitrate solution was impregnated by planetary mixer (P-mixer) onto the stabilized alumina to form a wet powder while achieving incipient wetness.
- the amounts of Pd was chosen to achieve final concentration of 85.5 g/ft 3 of Pd.
- An aqueous slurry was formed by combining all of the above components with water, and milling to a particle size of 90% less than 10 microns.
- the slurry was coated onto a cordierite carrier using deposition methods known in the art for depositing the catalyst on a cordierite substrate. After coating, the carrier plus the inner layer were dried and then calcined at a temperature of 500 0 C for about 1 hour.
- the components present in the middle layer were high surface area gamma alumina doped with 4% of lanthanum, a ceria-zirconia composite with 28% ceria by weight, zirconium oxide, and barium oxide, at concentrations of approximately
- the barium oxide was introduced as an acetate colloidal solution.
- the total loading of the middle layer was 1.65 g/in 3 .
- Rhodium in the form of a Rhodium nitrate solution was impregnated by planetary mixer (P-mixer) onto the stabilized alumina to form a wet powder while achieving incipient wetness.
- the amounts of Rh was chosen to achieve final concentration of 2 g/ft 3 of Rh.
- An aqueous slurry was formed by combining ail of the above components with water, and milling to a particle size of 90% less than 10 mi- crons.
- the slurry was coated onto the cordierite carrier over the inner layer using deposition methods known in the art for depositing the catalyst on a cordierite substrate. After coating, the carrier plus the inner and middle layers were dried, and then calcined at a temperature of 550°C for about 1 hour.
- the components present in the outer layer were high surface area gamma alumina doped with 20% of zirconium oxide, zirconium oxide and binder, at concentrations of approximately 94%, 2,4% and 2,4% , respectively, based on the cal- cined weight of the catalyst.
- the total loading of the middle layer was 1 g/in 3 .
- Platinum in the form of a platinum tetra methyl ammonium hydroxide complex solution was impregnated by planetary mixer (P-mixer) and subsequently Palladium in the form of a Palladium nitrate solution was impregnated onto the stabilized alumina to form a wet powder while achieving incipient wetness.
- Pt and Pd where chosen to achieve final concentration of 8 g/ft 3 of Pt and 9,5 g/ft 3 of Pd.
- An aqueous slurry was formed by combining all of the above components with water, and milling to a particle size of 90% less than 10 microns.
- the slurry was coated onto the cordierite carrier over the inner layer using deposition meth- ods known in the art for depositing the catalyst on a cordierite substrate. After coating, the carrier plus the inner and middle layers were dried, and then calcined at a temperature of 55O 0 C for about 1 hour.
- the components present in the inner layer were high surface area gamma alu- mina doped with 4% of lanthanum, a ceria-zirconia composite with 45% ceria by weight, zirconium oxide, barium oxide and a binder, at concentrations of approximately 67%, 18%, 3%, 6% and 3%, respectively, based on the calcined weight of the catalyst.
- the total loading of the inner layer was 1.60 g/in 3 .
- the zirconium oxide was introduced as an acetate colloidal solution and the barium ox- ide as barium acetate solution.
- Palladium in the form of a Palladium nitrate solution was impregnated by planetary mixer (P-mixer) onto the stabilized alumina to form a wet powder while achieving incipient wetness.
- the amounts of Pd was chosen to achieve final con- centration of 66 g/ft 3 of Pd.
- An aqueous slurry was formed by combining all of the above components with water, and milling to a particle size of 90% less than 10 microns.
- the slurry was coated onto a cordierite carrier using deposition methods known in the art for depositing the catalyst on a cordierite substrate. After coating, the carrier plus the inner layer were dried and then calcined at a temperature of 500 0 C for about 1 hour.
- the components present in the middle layer were high surface area gamma alu- mina doped with 4% of lanthanum, a ceria-zirconia composite with 28% ceria by weight, zirconium oxide, and barium oxide, at concentrations of approximately 49%, 49%, 1.5%, 1.5% and 3%, respectively, based on the calcined weight of the catalyst.
- the barium oxide was introduced as an acetate colloidal solution.
- the total loading of the middle layer was 1.65 g/in 3 .
- Rhodium in the form of a Rhodium nitrate solution was impregnated by planetary mixer (P-mixer) onto the stabilized alumina to form a wet powder while achieving incipient wetness.
- the amounts of Rh was chosen to achieve final concentration of 2 g/ft 3 of Rh
- An aqueous slurry was formed by combining all of the above components with water, and milling to a particle size of 90% less than 10 mi- crons.
- the slurry was coated onto the cordierite carrier over the inner layer using deposition methods known in the art for depositing the catalyst on a cordierite substrate. After coating, the carrier plus the inner and middle layers were dried, and then calcined at a temperature of 550 0 C for about 1 hour.
- the components present in the outer layer were high surface area gamma alumina doped with 20% of zirconium oxide, zirconium oxide and binder, at concen- trations of approximately 94%, 2.4% and 2.4% , respectively, based on the calcined weight of the catalyst.
- the total loading of the middle layer was 1 g/in 3 .
- Palladium in the form of a Palladium nitrate solution was impregnated by planetary mixer (P-mixer) onto the stabilized alumina to form a wet powder while achieving incipient wetness.
- the amounts of Pd was chosen to achieve final concentration of 36 g/ff of Pd
- An aqueous slurry was formed by combining all of the above components with water, and milling to a particle size of 90% less than 10 microns.
- the slurry was coated onto the cordierite carrier over the inner layer using deposition methods known in the art for depositing the catalyst on a cordierite substrate. After coating, the carrier plus the inner and middle layers were dried, and then calcined at a temperature of 550 0 C for about 1 hour.
- the components present in the inner layer were high surface area gamma alumina doped with 4% of lanthanum, a ceria-zirconia composite with 45% ceria by weight, zirconium oxide, barium oxide and a binder, at concentrations of approximately 67%, 18%, 3%, 6% and 3%, respectively, based on the calcined weight of the catalyst.
- the total loading of the inner layer was 1.649 g/in 3 .
- the zirconium oxide was introduced as an acetate colloidal solution and the barium oxide as barium acetate solution.
- Palladium in the form of a Palladium nitrate solution was impregnated by planetary mixer (P-mixer) onto the stabilized alumina to form a wet powder while achieving incipient wetness.
- the amounts of Pd was chosen to achieve final concentration of 93 g/ft 3 of Pd.
- An aqueous slurry was formed by combining all of the above components with water, and milling to a particle size of 90% less than 10 microns.
- the slurry was coated onto a cordierite carrier using deposition methods known in the art for depositing the catalyst on a cordierite substrate. After coating, the carrier plus the inner layer were dried and then calcined at a temperature of 500 0 C for about 1 hour.
- the components present in the middle layer were high surface area gamma alumina doped with 4% of lanthanum, a ceria-zirconia composite with 28% ceria by weight, zirconium oxide, and barium oxide, at concentrations of approximately
- the barium oxide was introduced as an acetate colloidal solution.
- the total loading of the middle layer was 1.65 g/in 3 .
- Rhodium in the form of a Rhodium nitrate solution was impregnated by planetary mixer (P-mixer) onto the stabilized alumina to form a wet powder while achieving incipient wetness.
- the amounts of Rh was chosen to achieve final concentration of 2 g/ft 3 of Rh.
- An aqueous slurry was formed by combining all of the above components with water, and milling to a particle size of 90% less than 10 mi- crons.
- the slurry was coated onto the cordierite carrier over the inner layer using deposition methods known in the art for depositing the catalyst on a cordierite substrate. After coating, the carrier plus the inner and middle layers were dried, and then calcined at a temperature of 550 0 C for about 1 hour.
- the components present in the outer layer were high surface area gamma alumina doped with 20% of zirconium oxide, zirconium oxide and binder, at concentrations of approximately 94%, 2,4% and 2,4% , respectively, based on the cal- cined weight of the catalyst.
- the total loading of the middle layer was 1 g/in 3 .
- Platinum in the form of a platinum tetra methyl ammonium hydroxide complex solution was impregnated by planetary mixer (P-mixer) and subsequently Palladium in the form of a Palladium nitrate solution was impregnated onto the stabilized alumina to form a wet powder while achieving incipient wetness.
- Pt and Pd where chosen to achieve final concentration of 8 g/ft 3 of Pt and 2 g/ft 3 of Pd.
- An aqueous slurry was formed by combining all of the above components with water, and milling to a particle size of 90% less than 10 microns.
- the slurry was coated onto the cordierite carrier over the inner layer using deposition meth- ods known in the art for depositing the catalyst on a cordierite substrate. After coating, the carrier plus the inner and middle layers were dried, and then calcined at a temperature of 550 0 C for about 1 hour.
- the components present in the inner layer were high surface area gamma alu- mina doped with 4% of lanthanum, a ceria-zirconia composite with 45% ceria by weight, zirconium oxide, barium oxide and a binder, at concentrations of approximately 67%, 18%, 3%, 6% and 3%, respectively, based on the calcined weight of the catalyst.
- the total loading of the inner layer was 1,649 g/in 3 .
- the zirconium oxide was introduced as an acetate colloidal solution and the barium oxide as barium acetate solution.
- Palladium in the form of a Palladium nitrate solution was impregnated by planetary mixer (P-mixer) onto the stabilized alumina to form a wet powder while achieving incipient wetness.
- the amounts of Pd was chosen to achieve final con- centration of 55 g/ft 3 of Pd.
- An aqueous slurry was formed by combining all of the above components with water, and milling to a particle size of 90% less than 10 microns.
- the slurry was coated onto a cordierite carrier using deposition methods known in the art for depositing the catalyst on a cordierite substrate. After coating, the carrier plus the inner layer were dried and then calcined at a temperature of 500 0 C for about 1 hour.
- the components present in the middle layer were high surface area gamma alu- mina doped with 4% of lanthanum, a ceria-zirconia composite with 28% ceria by weight, zirconium oxide, and barium oxide, at concentrations of approximately 49%, 49%, 1 ,5%, 1,5% and 3%, respectively, based on the calcined weight of the catalyst.
- the barium oxide was introduced as an acetate colloidal solution.
- the total loading of the middle layer was 1.65 g/in 3 .
- Rhodium in the form of a Rhodium nitrate solution was impregnated by planetary mixer (P-mixer) onto the stabilized alumina to form a wet powder while achieving incipient wetness.
- the amounts of Rh was chosen to achieve final concentration of 2 g/ft 3 of Rh.
- An aqueous slurry was formed by combining all of the above components with water, and milling to a particle size of 90% less than 10 mi- crons.
- the slurry was coated onto the cordierite carrier over the inner layer using deposition methods known in the art for depositing the catalyst on a cordierite substrate. After coating, the carrier plus the inner and middle layers were dried, and then calcined at a temperature of 550 0 C for about 1 hour.
- the components present in the outer layer were high surface area gamma alumina doped with 20% of zirconium oxide, zirconium oxide and binder, at concen- trations of approximately 94%, 2,4% and 2,4% , respectively, based on the calcined weight of the catalyst.
- the total loading of the middle layer was 1 g/in 3 .
- Platinum in the form of a platinum tetra methyl ammonium hydroxide complex solution was impregnated by planetary mixer (P-mixer) and subsequently Palladium in the form of a Palladium nitrate solution was impregnated onto the stabilized alumina to form a wet powder while achieving incipient wetness.
- the amounts of Pt and Pd where chosen to achieve final concentration of 8 g/ft 3 of Pt and 40 g/ft 3 of Pd.
- An aqueous slurry was formed by combining all of the above components with water, and milling to a particle size of 90% less than 10 microns.
- the slurry was coated onto the cordierite carrier over the inner layer using deposition methods known in the art for depositing the catalyst on a cordierite substrate. After coating, the carrier plus the inner and middle layers were dried, and then calcined at a temperature of 550 0 C for about 1 hour.
- the components present in the inner layer were high surface area gamma alumina, a ceria-zirconia composite with 45% ceria by weight, zirconium oxide and a binder, at concentrations of approximately 23%, 70%, 0.5% and 0.3%, respectively, based on the calcined weight of the catalyst.
- the total loading of the inner layer was 1.075 g/in 3 .
- the zirconium oxide was introduced as an acetate colloidal solution and the barium oxide as barium acetate solution.
- aqueous slurry was formed by combining all of the above components with water, and milling to a particle size of 90% less than 10 microns.
- the slurry was coated onto a cordierite carrier using deposition methods known in the art for de- positing the catalyst on a cordierite substrate. After coating, the carrier plus the inner layer were dried and then calcined at a temperature of 500 0 C for about 1 hour,
- the components present in the middle layer were high surface area gamma alumina doped with 4% of lanthanum, a ceria-zirconia composite with 28% ceria by weight, and barium oxide, at concentrations of approximately 59%, 36%, and 5% respectively, based on the calcined weight of the catalyst.
- the barium oxide was introduced as an acetate colloidal solution.
- the total loading of the middle layer was 2.05 g/in 3 .
- Palladium in the form of a Palladium nitrate solution was impregnated by planetary mixer (P-mixer) onto the stabilized alumina to form a wet powder while achieving incipient wetness.
- the amounts of Pd was chosen to achieve final concentration of 95g/ft 3 of Pd.
- An aqueous slurry was formed by combining all of the above components with water, and milling to a particle size of 90% less than 10 microns.
- the slurry was coated onto the cordierite carrier over the inner layer using deposition methods known in the art for depositing the catalyst on a cordierite substrate. After coating, the carrier plus the inner and middle layers were dried, and then calcined at a temperature of 550 0 C for about 1 hour.
- the components present in the outer layer were high surface area gamma alumina doped, a ceria-zirconia composite with 45% ceria by weight, zirconium oxide, barium oxide and a binder, at concentrations of approximately 78%, 16%, 3%, 3% and 3%, respectively, based on the calcined weight of the catalyst, zirconium oxide and binder, at concentrations of approximately 94%, 2.4% and 2.4% , respectively, based on the calcined weight of the catalyst.
- the total loading of the middle layer was 1.6 g/in 3 .
- Rhodium in the form of a Rhodium nitrate solution and Platinum in the form of a platinum tetra methyl ammonium hydroxide complex solution was impregnated by planetary mixer (P-mixer) onto the stabilized alumina to form a wet powder while achieving incipient wetness.
- the amounts of Pt and Rh where chosen to achieve final concentration of 8 g/ft 3 of Pt and 2 g/ft 3 of Rh.
- An aqueous slurry was formed by combining all of the above components with water, and milling to a particle size of 90% less than 10 microns.
- the slurry was coated onto the cordierite car- rier over the inner layer using deposition methods known in the art for depositing the catalyst on a cordierite substrate. After coating, the carrier plus the inner and middle layers were dried, and then calcined at a temperature of 55O 0 C for about 1 hour.
- the components present in the inner layer were high surface area gamma alumina doped, barium oxide and lanthanum oxide, at concentrations of approximately 93%, 5%, and 3% respectively, based on the calcined weight of the catalyst.
- the barium oxide was introduced as an acetate colloidal solution.
- the total loading of the bottom layer was 1.85 g/in 3 .
- Palladium in the form of a Palladium nitrate solution was impregnated by planetary mixer (P-mixer) onto the stabilized alumina to form a wet powder while achieving incipient wetness.
- the amounts of Pd was chosen to achieve final concentration of 100 g/ft 3 of Pd.
- An aqueous slurry was formed by combining all of the above components with water, and milling to a particle size of 90% less than
- the slurry was coated onto the cordierite carrier over the inner layer using deposition methods known in the art for depositing the catalyst on a cordierite substrate. After coating, the carrier plus the inner and middle layers were dried, and then calcined at a temperature of 55O 0 C for about 1 hour.
- the components present in the outer layer were high surface area gamma alumina doped, a ceria-zirconia composite with 10% ceria by weight, barium oxide and a binder, at concentrations of approximately 58%, 36%, 2%, and 3%, respectively, based on the calcined weight of the catalyst.
- the total loading of the middle layer was 2.59 g/in 3 .
- Rhodium in the form of a Rhodium nitrate solution and Palladium in the form of a Palladium nitrate solution was impregnated separately by planetary mixer (P- mixer) onto the stabilized alumina to form a wet powder while achieving incipient wetness.
- the amounts of Pd and Rh where chosen to achieve final concentration of 3.5g/ft 3 of Pd and 10 g/ft 3 of Rh.
- An aqueous slurry was formed by combining all of the above components with water, and milling to a particle size of 90% less than 10 microns.
- the slurry was coated onto the cordierite carrier over the inner iayer using deposition methods known in the art for depositing the catalyst on a cordierite substrate. After coating, the carrier plus the inner and middle layers were dried, and then calcined at a temperature of 550 0 C for about 1 hour.
- the components present in the inner layer were high surface area gamma alumina doped with 4% of lanthanum, zirconium oxide, barium oxide and a binder, at concentrations of approximately 88%, 3%, 6%, 3%, respectively, based on the calcined weight of the catalyst.
- the total loading of the inner layer was 1,70 g/in 3 .
- the zirconium oxide was introduced as an acetate colloidal solution and the bar- ium oxide as barium acetate solution.
- Palladium in the form of a Palladium nitrate solution was impregnated by planetary mixer (P-mixer) onto the stabilized alumina to form a wet powder while achieving incipient wetness.
- the amounts of Pd was chosen to achieve final con- centration of 82 g/ft 3 of Pd.
- An aqueous slurry was formed by combining ail of the above components with water, and milling to a particle size of 90% less than 10 microns.
- the slurry was coated onto a cordierite carrier using deposition methods known in the art for depositing the catalyst on a cordierite substrate. After coating, the carrier plus the inner layer were dried and then calcined at a temperature of 500 0 C for about 1 hour.
- the components present in the middle layer were high surface area gamma alu- mina doped with 20% of zriconia, a ceria-zirconia composite with 28% ceria by weight, zirconium oxide, and barium oxide, at concentrations of approximately 49%, 49%, 1.5%, 1.5% and 3%, respectively, based on the calcined weight of the catalyst.
- the barium oxide was introduced as an acetate colloidal solution.
- the total loading of the middle layer was 1.65 g/in 3 .
- Rhodium in the form of a Rhodium nitrate solution was impregnated by planetary mixer (P-mixer) onto the stabilized alumina to form a wet powder while achieving incipient wetness.
- the amounts of Rh was chosen to achieve final concentration of 6 g/ft 3 of Rh.
- An aqueous slurry was formed by combining all of the above components with water, and milling to a particle size of 90% less than 10 mi- crons.
- the slurry was coated onto the cordierite carrier over the inner layer using deposition methods known in the art for depositing the catalyst on a cordierite substrate. After coating, the carrier plus the inner and middle layers were dried, and then calcined at a temperature of 55O 0 C for about 1 hour.
- the components present in the outer layer were high surface area gamma alumina doped with 0.4% of lanthanum oxide, a ceria-zirconia composite with 28% ceria by weight, barium oxide, zirconium oxide and binder, at concentrations of approximately 65%, 28%, 2%, 2% and 2 % , respectively, based on the calcined weight of the catalyst.
- the total loading of the outer layer was 1.1 g/in 3 .
- Palladium in the form of a Palladium nitrate solution was impregnated by plane- tary mixer (P-mixer) onto the stabilized alumina to form a wet powder while achieving incipient wetness.
- the amounts of Pd was chosen to achieve final concentration of 2g/ft 3 of Pd.
- An aqueous slurry was formed by combining all of the above components with water, and milling to a particle size of 90% less than 10 microns.
- the slurry was coated onto the cordierite carrier over the inner layer us- ing deposition methods known in the art for depositing the catalyst on a cordierite substrate. After coating, the carrier plus the inner and middle layers were dried, and then calcined at a temperature of 550 0 C for about 1 hour.
- the catalysts were aged prior to test for 25 h at 950 0 C maximum catalyst bed temperature with secondary air injection. This procedure yield in intervals of 25 seconds at 950 0 C bed temperature at lambda 1 and 8 seconds at Lambda 2 with a minimum temperature at 65O 0 C.
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Application Number | Priority Date | Filing Date | Title |
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JP2012508823A JP5651685B2 (en) | 2009-05-04 | 2010-05-04 | Improved lean HC conversion of TWC for lean burn gasoline engine |
US12/810,140 US8906330B2 (en) | 2009-05-04 | 2010-05-04 | Lean HC conversion of TWC for lean burn gasoline engines |
KR1020117026191A KR101712684B1 (en) | 2009-05-04 | 2010-05-04 | Improved lean hc conversion of twc for lean burn gasoline engines |
CN201080019754.1A CN102414412B (en) | 2009-05-04 | 2010-05-04 | Improved lean HC conversion of TWC for lean burn gasoline engines |
BRPI1014604A BRPI1014604A2 (en) | 2009-05-04 | 2010-05-04 | catalyst composition, and method for treating a discharge gas stream |
EP10772658.0A EP2427637B1 (en) | 2009-05-04 | 2010-05-04 | Improved lean hc conversion of twc for lean burn gasoline engines |
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US17531209P | 2009-05-04 | 2009-05-04 | |
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EP2695673A1 (en) * | 2011-04-08 | 2014-02-12 | Toyota Jidosha Kabushiki Kaisha | Exhaust gas purification catalyst |
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JP2017127867A (en) * | 2011-05-13 | 2017-07-27 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | Catalyzed soot filter with layered design |
WO2013021395A1 (en) * | 2011-08-10 | 2013-02-14 | Süd-Chemie India Ltd. | Catalyst for after-treatment of exhaust gas from an internal combustion engine |
WO2013093597A3 (en) * | 2011-12-22 | 2013-08-22 | Johnson Matthey Public Limited Company | Improved nox trap |
CN104039425A (en) * | 2011-12-22 | 2014-09-10 | 庄信万丰股份有限公司 | Improved NOx trap |
JP2015502855A (en) * | 2011-12-22 | 2015-01-29 | ジョンソン、マッセイ、パブリック、リミテッド、カンパニーJohnson Matthey Publiclimited Company | Improved NOx trap |
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WO2023031584A1 (en) * | 2021-08-31 | 2023-03-09 | Johnson Matthey Public Limited Company | Transition metal incorporated alumina for improved three way catalysts |
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US11986802B2 (en) | 2021-08-31 | 2024-05-21 | Johnson Matthey Public Limited Company | Transition metal incorporated alumina for improved three way catalysts |
Also Published As
Publication number | Publication date |
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US20130189173A1 (en) | 2013-07-25 |
KR101712684B1 (en) | 2017-03-06 |
EP2427637A4 (en) | 2015-03-25 |
KR20120024581A (en) | 2012-03-14 |
US8906330B2 (en) | 2014-12-09 |
EP2427637A2 (en) | 2012-03-14 |
EP2427637B1 (en) | 2017-03-08 |
CN102414412A (en) | 2012-04-11 |
CN102414412B (en) | 2014-12-31 |
JP2012525955A (en) | 2012-10-25 |
BRPI1014604A2 (en) | 2016-04-05 |
JP5651685B2 (en) | 2015-01-14 |
WO2010129490A3 (en) | 2011-04-14 |
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