WO2011062129A1 - 排ガス浄化用触媒及びその製造方法 - Google Patents
排ガス浄化用触媒及びその製造方法 Download PDFInfo
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- WO2011062129A1 WO2011062129A1 PCT/JP2010/070265 JP2010070265W WO2011062129A1 WO 2011062129 A1 WO2011062129 A1 WO 2011062129A1 JP 2010070265 W JP2010070265 W JP 2010070265W WO 2011062129 A1 WO2011062129 A1 WO 2011062129A1
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- catalyst
- exhaust gas
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- B01D2255/1025—Rhodium
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- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
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- B01D2255/2092—Aluminium
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- B01D2255/908—O2-storage component incorporated in the catalyst
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- 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
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- 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 an exhaust gas purifying catalyst for purifying exhaust gas discharged from an internal combustion engine and a method for manufacturing the same. More specifically, the present invention relates to an exhaust gas purifying catalyst capable of purifying nitrogen oxide contained in exhaust gas with high efficiency and a method for producing the same.
- a three-way catalyst that oxidizes or reduces harmful gases (hydrocarbon (HC), carbon monoxide (CO), and nitrogen oxide (NOx)) contained in exhaust gas is known as an exhaust gas purification catalyst mounted on automobiles. It has been. Due to the recent increase in environmental awareness, regulations on exhaust gas emitted from automobiles and the like have been further strengthened, and the three-way catalyst has been improved accordingly.
- a catalyst powder containing a covered cocatalyst inclusion body is disclosed (for example, see Patent Document 1).
- the promoter component particles are covered with a heat-resistant oxide, the aggregation of the promoter component particles and the decrease in the specific surface area are suppressed, and high durability can be exhibited.
- the pore diameter between the particles of the catalyst powder in the catalyst layer is the high heat-resistant oxide covering the promoter particles. It is much larger than the pore diameter. Therefore, the exhaust gas flowing into the catalyst layer from the inlet of the honeycomb carrier is more likely to pass through the pores between the catalyst powders than the pores of the high heat resistant oxide. Therefore, for example, when the exhaust gas is in excess of oxygen, oxygen reaches the deep part of the catalyst layer before the promoter component enclosed by the high heat-resistant oxide completely absorbs oxygen. For this reason, since oxygen is excessively present around the catalyst powder in the deep part of the catalyst layer, it may be difficult to reduce the nitrogen oxides. Further, when the air-fuel ratio (A / F) of the exhaust gas fluctuates, the A / F fluctuation cannot be absorbed only by the upper part of the catalyst layer, and the purification rate of the exhaust gas sometimes decreases.
- a / F air-fuel ratio
- the present invention has been made in view of such problems of the conventional technology.
- the object of the present invention is to purify nitrogen oxide with high efficiency even when oxygen is excessive, for example, when the fuel supply to the internal combustion engine is stopped and only the air is exhausted.
- the object is to provide a catalyst for exhaust gas purification.
- the objective of this invention is providing the manufacturing method which can manufacture the said exhaust gas purification catalyst by a simple method.
- the exhaust gas purifying catalyst according to the first aspect of the present invention is a catalyst unit including noble metal particles and anchor particles supporting noble metal particles as an anchor material for the noble metal particles, and is disposed in non-contact with the noble metal particles.
- a co-catalyst unit including first co-catalyst particles having oxygen storage / release capability; and both the catalyst unit and the co-catalyst unit are included, and noble metal particles and anchor particles in the catalyst unit and An anchor / promoter simultaneous inclusion particle containing an inclusion material separating the promoter particle from each other.
- the exhaust gas purifying catalyst includes second promoter particles having an oxygen storage / release capability and not included in the anchor / promoter simultaneous inclusion particles by the inclusion material.
- the exhaust gas purifying catalyst according to the second aspect of the present invention is a catalyst unit including noble metal particles and anchor particles supporting noble metal particles as an anchor material for the noble metal particles, and is disposed in non-contact with the noble metal particles.
- a co-catalyst unit including first co-catalyst particles having oxygen storage / release capability; and both the catalyst unit and the co-catalyst unit are included, and noble metal particles and anchor particles in the catalyst unit and A plurality of anchor / promoter simultaneous inclusion particles containing an inclusion material separating the promoter particles from each other.
- the exhaust gas purifying catalyst includes second promoter particles having an oxygen storage / release capability and not included in the anchor / promoter simultaneous inclusion particles by the inclusion material. The second promoter particles are arranged in pores formed between the plurality of anchor / promoter simultaneous inclusion particles.
- the method for producing an exhaust gas purifying catalyst according to the third aspect of the present invention includes a step of individually or integrally pulverizing composite particles of first metal particles and anchor particles and first promoter particles, and the pulverized composite
- the method includes a step of preparing the anchor / promoter simultaneous inclusion particles by mixing the particles and the first promoter particles with a slurry containing a precursor of the inclusion material and drying.
- the manufacturing method includes a step of mixing and pulverizing the anchor / promoter simultaneous inclusion particles and the second promoter particles.
- FIG. 1 is a schematic view showing an exhaust gas purifying catalyst according to an embodiment of the present invention
- FIG. 1 (a) is a perspective view showing the exhaust gas purifying catalyst
- FIG. 1 (b) is a diagram of FIG.
- FIG. 1C is an enlarged schematic view of the portion B
- FIG. 1C is an enlarged schematic view of the portion C in FIG. 1B
- FIG. 1D is a view of the reference D in FIG. It is the schematic which expanded the part of.
- FIG. 2 shows the ratio Da / Db between the average particle diameter Da of the composite particles before the exhaust durability test and the average pore diameter Db of the clathrate, and the CeO 2 crystal growth ratio and the surface area of Pt after the exhaust durability test.
- FIG. 3 is a graph showing the relationship between the particle diameter and surface area of the noble metal.
- FIG. 4 is a graph showing the relationship between the particle size of the noble metal, the number of atoms, and the surface area.
- FIG. 5 is a photomicrograph showing the distance between the anchor particles and the first promoter particles in the anchor / promoter simultaneous inclusion particles.
- FIG. 6 is a graph showing the relationship between the center-to-center distance between the catalyst unit and the promoter unit and the appearance frequency.
- FIG. 7 is a schematic view showing examples of anchor / promoter simultaneous inclusion particles having different degrees of dispersion.
- FIG. 8 is a schematic view showing an exhaust gas purification system according to an embodiment of the present invention.
- FIG. 8 is a schematic view showing an exhaust gas purification system according to an embodiment of the present invention.
- FIG. 9 is a graph showing the relationship between the weight ratio of the first promoter particles to the total weight of the first and second promoter particles and the NOx residual ratio.
- FIG. 10 is a graph showing the relationship between the center-to-center distance between the catalyst unit and the promoter unit and the NOx conversion rate.
- FIG. 1 shows an exhaust gas purifying catalyst (hereinafter also referred to as catalyst) 1 according to an embodiment of the present invention.
- the exhaust gas-purifying catalyst 1 includes a honeycomb carrier (refractory inorganic carrier) 2 having a plurality of cells 2a. The exhaust gas flows through each cell 2a along the exhaust gas flow direction F, and is purified by contacting with the catalyst layer there.
- the exhaust gas-purifying catalyst 1 is formed by forming a catalyst layer on the inner surface of the carrier 2. Specifically, as shown in FIG. 1B, the catalyst layer 3 and the undercoat layer 4 are formed on the inner surface of the carrier 2.
- the catalyst layer 3 is formed of a catalyst powder 7 containing a plurality of anchor / promoter simultaneous inclusion particles 5 and a plurality of second promoter particles 6 as shown in FIG. Yes.
- anchor / promoter simultaneous inclusion particles 5 and the second promoter particles 6 will be described in detail.
- the anchor / promoter simultaneous enclosure particles 5 are composed of noble metal particles 8, anchor particles 9, and first promoter particles 11. Containing.
- the anchor particles 9 carry the noble metal particles 8 on the surface as an anchor material for the noble metal particles 8.
- the first promoter particles 11 are disposed in non-contact with the noble metal particles 8 and have an oxygen storage / release capability.
- the encapsulated particles 5 enclose the composite particles 10 of the noble metal particles 8 and the anchor particles 9 and the first promoter particles 11 together, and include the inclusion material 12 that separates the composite particles 10 and the first promoter particles 11 from each other. contains.
- the anchor particles 9 act as an anchor material for chemical bonding, and the movement of the noble metal particles 8 is suppressed. Further, the anchor particles 9 carrying the noble metal particles 8 are covered with the inclusion material 12 so as to be included, so that the movement of the noble metal particles 8 beyond the section separated by the inclusion material 12 is physically performed. To suppress. Further, by including the anchor particles 9 in the section separated by the enclosure material 12, the anchor particles 9 are prevented from contacting and aggregating beyond the section separated by the enclosure material 12. This not only prevents the anchor particles 9 from aggregating, but also prevents the noble metal particles 8 supported on the anchor particles 9 from aggregating.
- the co-inclusion particles 5 can suppress a decrease in catalytic activity due to aggregation of the noble metal particles 8 without increasing the manufacturing cost and environmental load. Moreover, the activity improvement effect of the noble metal particle 8 by the anchor particle 9 can be maintained.
- the physical movement of the first promoter particles 11 is also suppressed by covering the first promoter particles 11 having the ability to store and release oxygen with the inclusion material 12 and encapsulating them. To do. That is, by including the first promoter particles 11 in the compartments separated by the enclosure material 12, the first promoter particles 11 come into contact with each other and aggregate over the compartments separated by the enclosure material 12. It can suppress and the fall of a specific surface area can be prevented.
- the anchor particles 9 and the first promoter particles 11 may exist as primary particles in a region separated by the inclusion material 12. That is, the catalyst unit 13 may contain the precious metal particles 8 and the primary particles of the anchor particles 9, and the promoter unit 14 may contain the primary particles of the first promoter particles 11. .
- the catalyst unit 13 may be composed of noble metal particles 8 and anchor particles 9.
- the promoter unit 14 may also be composed of the first promoter particles 11.
- the noble metal particles 8 include at least one selected from platinum (Pt), palladium (Pd), rhodium (Rh), gold (Au), silver (Ag), iridium (Ir), and ruthenium (Ru). Can be used. Among these, in particular, platinum (Pt), palladium (Pd), and rhodium (Rh) can exhibit high NOx purification performance.
- the anchor particles 9 include aluminum oxide (Al 2 O 3 ), cerium oxide (CeO 2 ), zirconium oxide (ZrO 2 ), yttrium oxide (Y 2 O 3 ), and neodymium oxide (Nd 2 O 3 ). At least one selected from can be the main component. Among these, since Al 2 O 3 and ZrO 2 are excellent in high temperature heat resistance and can maintain a high specific surface area, it is preferable that the anchor particles 9 have Al 2 O 3 or ZrO 2 as a main component. In the present specification, the main component means a component having a content of 50 atomic percent or more in the particles.
- the first promoter particles 11 preferably contain at least one of cerium (Ce) and praseodymium (Pr) having oxygen storage / release capability.
- the first promoter particles are preferably composed mainly of a compound having a high oxygen storage / release capability, such as cerium oxide (CeO 2 ) or praseodymium oxide (Pr 6 O 11 ).
- Ce and Pr both have a plurality of valences, and the oxidation number changes due to fluctuations in the exhaust gas atmosphere. Therefore, Ce and Pr are materials that can store and release active oxygen.
- the enclosure material 12 preferably contains at least one of aluminum (Al) and silicon (Si).
- the inclusion material 12 is preferably a material that can include the anchor particles and the first promoter particles and ensure gas permeability. From such a viewpoint, a compound containing at least one of Al and Si, such as Al 2 O 3 and SiO 2 , has a large pore volume and can ensure high gas diffusibility. Therefore, it is preferable that the enclosure material 12 is mainly composed of Al 2 O 3 and SiO 2 .
- the inclusion material may be a composite compound of Al and Si.
- the enclosure material 12 used in the anchor / promoter simultaneous enclosure particles 5 does not completely surround the catalyst unit 13 and the promoter unit 14.
- the enclosure material 12 has pores that allow the exhaust gas and active oxygen to pass through while covering the catalyst unit 13 and the promoter unit 14 so as to suppress physical movement of each.
- the enclosure material 12 appropriately encloses the catalyst unit 13 and the co-catalyst unit 14 and suppresses aggregation of particles in each unit.
- the enclosure material 12 has a plurality of pores 12a, exhaust gas and active oxygen can pass therethrough.
- the pore diameter of the pores 12a is preferably 30 nm or less, and more preferably 10 nm to 30 nm. This pore diameter can be determined by a gas adsorption method.
- alumina or silica can be used as such an inclusion material 12.
- the clathrate is made of alumina, it is preferable to use boehmite (AlOOH) as a precursor. That is, the anchor particles 9 carrying the noble metal particles 8 and the first promoter particles 11 are put into a slurry in which boehmite is dispersed in a solvent such as water and stirred. Thereby, boehmite adheres around the anchor particles 9 and the first promoter particles 11. Then, by drying and firing this mixed slurry, boehmite is dehydrated and condensed around the anchor particles 9 and the first promoter particles 11, and an inclusion material made of boehmite-derived ⁇ -alumina is formed.
- Such a clathrate made of boehmite-derived alumina has excellent gas permeability because it has many pores of 30 nm or less while covering the anchor particles 9 and the first promoter particles 11. .
- silica sol and zeolite as precursors.
- the anchor particles 9 carrying the noble metal particles 8 and the first promoter particles 11 are put into a slurry in which silica sol and zeolite are dispersed in a solvent, stirred, dried and fired, whereby a clathrate made of silica. Is formed.
- a clathrate made of silica sol and zeolite-derived silica also has excellent gas permeability because it has many pores of 30 nm or less while covering the anchor particles 9 and the first promoter particles 11. Yes.
- the average particle diameter of the catalyst unit 13 included in the section separated by the inclusion material 12 is 300 nm or less. Therefore, it is preferable that the average secondary particle diameter of the anchor particles 9 included in the catalyst unit 13 is also 300 nm or less. In this case, when rhodium is used as the noble metal, it is possible to supply active oxygen while maintaining the reduced state of rhodium.
- the average particle diameter of the catalyst unit 13 and the average secondary particle diameter of the anchor particles are more preferably 200 nm or less. As a result, the amount of noble metal supported on the secondary particles of the anchor particles is further reduced, so that aggregation of noble metals can be suppressed.
- the minimum of the average particle diameter of the catalyst unit 13 and the average secondary particle diameter of the anchor particle 9 is not specifically limited.
- the average particle diameter of the catalyst unit 13 is preferably larger than the average pore diameter of the pores 12 a formed in the enclosure material 12. Therefore, it is preferable that the average particle diameter of the catalyst unit 13 and the average secondary particle diameter of the anchor particle 9 exceed 30 nm.
- the average particle diameter of the promoter unit 14 included in the compartments separated by the inclusion material 12 is preferably 1000 nm or less, and more preferably 300 nm or less. Therefore, the average secondary particle diameter of the first promoter particles 11 included in the promoter unit 14 is also preferably 1000 nm or less, and more preferably 300 nm or less. As a result, the surface area of the secondary particles is greatly improved, so that the supply rate of active oxygen is improved and the catalyst performance can be improved.
- the lower limit of the average particle diameter of the promoter unit 14 and the average secondary particle diameter of the first promoter particles 11 is not particularly limited as in the case of the anchor particles 9.
- the average particle diameter of the promoter unit 14 is preferably larger than the average pore diameter of the pores 12 a formed in the enclosure material 12. Therefore, it is preferable that the average particle diameter of the promoter unit 14 and the average secondary particle diameter of the first promoter particles 11 exceed 30 nm.
- the average secondary particle size of the anchor particles and the first promoter particles can be determined by applying a slurry containing these particles in a process of producing the inclusion particles to a laser diffraction type particle size distribution measuring device.
- the average secondary particle diameter in this case means a median diameter (D50).
- the average secondary particle diameter of these particles and the particle diameter of noble metal particles described later can also be measured from a TEM photograph of the produced inclusion particles.
- the average particle diameter of the catalyst unit 13 and the promoter unit 14 can also be measured from a TEM photograph.
- the average particle diameter of the noble metal particles 8 is preferably in the range of 2 nm to 10 nm.
- the average particle diameter of the noble metal particles 8 is 2 nm or more, sintering due to the movement of the noble metal particles 8 themselves can be reduced.
- the average particle diameter of the noble metal particles 8 is 10 nm or less, a decrease in reactivity with the exhaust gas can be suppressed.
- Db ⁇ Da means that the average particle diameter Da of the catalyst unit 13 is larger than the average diameter Db of the pores 12 a of the enclosure material 12.
- FIG. 2 shows the ratio Da / Db between the average particle diameter Da of the composite particle 10 before the exhaust durability test and the average pore diameter Db of the clathrate, and the ceria (CeO 2) as the anchor particle 9 after the exhaust durability test. ) And the surface area of platinum (Pt) as the noble metal particle 8 are plotted on the vertical axis to show these relationships. From FIG. 2, it can be seen that when Da / Db exceeds 1, the crystal growth ratio of CeO 2 is remarkably reduced and the sintering of CeO 2 is small. Further, it can be seen that even after the durability test, the surface area of Pt is maintained in a high state, and aggregation of Pt is suppressed.
- the average particle diameter Dc of the promoter unit 14 and the average pore diameter Db of the pores 12a formed in the enclosure material 12 enclosing the promoter unit 14 are Db. It is preferable to satisfy the relationship ⁇ Dc. That is, as shown in FIG. 1 (d), Db ⁇ Dc means that the average particle diameter Dc of the promoter unit 14 is larger than the average diameter Db of the pores 12 a of the enclosure material 12. .
- Db ⁇ Dc the movement of the first promoter particles 11 through the pores 12a formed in the enclosure material 12 is suppressed. Therefore, aggregation with the first promoter particles included in the other compartments can be reduced. As a result, since the surface area of the first promoter particles is maintained at a high level, it is possible to efficiently store and release active oxygen on the particle surfaces.
- the noble metal particles 8 are in contact with the anchor particles 9.
- the ratio of the noble metal particles 8 that are in contact with the anchor particles 9 is less than 80%, the noble metal particles 8 that do not exist on the anchor particles 9 increase, so that the sintering may proceed due to the movement of the noble metal particles 8.
- At least one of the anchor particles and the first promoter particles is preferably an oxide further containing at least one selected from iron (Fe), manganese (Mn), cobalt (Co), and nickel (Ni).
- the anchor particles 9 are mainly composed of alumina or zirconia
- the first promoter particles are mainly composed of cerium oxide or praseodymium oxide.
- At least one of the anchor particles and the first promoter particles further includes at least one NOx adsorbent selected from barium (Ba), magnesium (Mg), calcium (Ca), strontium (Sr), and sodium (Na). It is preferable to include. Any compound containing these elements acts as a NOx adsorbent. Therefore, the NOx purification performance can be improved by including the NOx adsorbent in at least one of the anchor particles and the first promoter particles. This is because the NOx adsorption reaction is very sensitive to gas contact.
- a catalyst containing these NOx adsorbents is suitable as a catalyst for a lean burn engine in which a large amount of NOx is generated than an engine that burns near the stoichiometric air-fuel ratio.
- the inclusion material is at least any one of cerium (Ce), zirconium (Zr), lanthanum (La), barium (Ba), magnesium (Mg), calcium (Ca), strontium (Sr), and sodium (Na).
- An oxide containing any one of these is preferable.
- cerium it is possible to give the inclusion material an oxygen storage / release capability and to improve exhaust gas purification performance.
- the heat resistance of an enclosure material can be improved by containing a zirconium and lanthanum.
- the NOx purification performance can be improved by containing a NOx adsorbent such as barium, magnesium, calcium, strontium and sodium in the clathrate.
- These elements can be contained by mixing the precursor slurry of the inclusion material with nitrates or acetates of these elements.
- the noble metal particle 8 is rhodium (Rh) and the anchor particle 9 is an oxide containing at least zirconium (Zr).
- Rh tends to have poor catalyst performance in a highly oxidized state, high oxidation and aggregation of Rh can be suppressed by appropriately adjusting the distance between the anchor particles and the first promoter particles.
- Rh binding energy analysis by X-ray photoelectron spectroscopy XPS
- Rh binding energy analysis by X-ray photoelectron spectroscopy XPS
- the 3d5 orbital binding energy of Rh is such that Rh in the metal state is 307.2 eV and Rh in the highly oxidized state is around 310.2 eV.
- an oxide such as Al 2 O 3 or ZrO 2
- the catalyst performance is lowered when the 3d5 orbital binding energy of Rh is 308.8 eV or more. Therefore, the 3d5 orbital coupling energy is 308. It is desirable that it is 8 eV or less.
- the 3d5 orbital binding energy of Rh can be reduced to 308.8 eV or less.
- it is common to perform charge correction using a certain element at the time of measurement of the binding energy and the binding energy of an element with a large content is corrected with respect to the literature value.
- a hydrocarbon contained in oil mist or the like derived from a pump for keeping the inside of the X-ray photoelectron spectrometer at a high vacuum is used, and the C1s peak of the hydrocarbon is compared with a literature value for correction.
- the anchor particle 9 is preferably an oxide containing zirconium as a main component.
- the anchor particles 9 are mainly composed of alumina or the like, rhodium and alumina are dissolved, rhodium is highly oxidized, and the catalytic activity may be lowered.
- Zr is contained in an oxide containing Zr, more preferably 50% or more in atomic percent in anchor particles, high oxidation and aggregation of Rh can be suppressed.
- Examples of such an oxide mainly containing Zr include zirconia (ZrO 2 ), lanthanum-added zirconia (Zr—La—O x ), and lanthanum-cerium-added zirconia (Zr—La—Ce—O x ). be able to.
- the compartments separated by the inclusion material 12 contain the noble metal particles 8 in a total amount of 8 ⁇ 10 ⁇ 20 mol or less. That is, the number of moles of the noble metal particles 8 in one catalyst unit 13 is preferably 8 ⁇ 10 ⁇ 20 moles or less.
- a plurality of noble metal particles 8 may move and aggregate together in a high temperature state. In this case, the noble metal particles 8 do not move to the enclosure material 12 due to the effect of the anchor particles 9, but aggregate into one or a plurality of noble metal particles on the surface of the anchor particles 9.
- FIG. 3 is a graph showing the relationship between the particle diameter and the surface area for platinum and palladium as noble metals. In the figure, since the same curve is shown in the case of platinum and palladium, it is shown as one curve. As apparent from FIG. 3, since the surface area is large if the particle diameter of the noble metal is 10 nm or less, it is possible to suppress the deterioration of the catalyst activity due to aggregation.
- FIG. 4 is a graph which shows the relationship between a particle diameter and the number of atoms regarding platinum and palladium as noble metals.
- the particle diameter is 10 nm
- the number of atoms of the noble metal is about 48000, and when this value is converted into the number of moles, it becomes about 8 ⁇ 10 ⁇ 20 moles.
- An example of a method for reducing the amount of noble metal contained in the catalyst unit 13 to 8 ⁇ 10 ⁇ 20 mol or less is to reduce the particle diameter of the anchor particles 9 carrying the noble metal particles 8.
- the adsorption stabilization energy of the noble metal particles 8 to the anchor particles 9 is Ea
- the adsorption stabilization energy of the noble metal particles 8 to the inclusion material 12 is Eb.
- Ea is preferably smaller than Eb (Ea ⁇ Eb).
- the difference (Eb ⁇ Ea) between the adsorption stabilization energy Ea of the noble metal particle 8 on the anchor particle 9 and the adsorption stabilization energy Eb of the noble metal particle 8 on the enclosure 12 exceeds 10.0 cal / mol. It is more preferable. When the adsorption stabilization energy difference exceeds 10.0 cal / mol, the movement of the noble metal particles 8 to the inclusion material 12 can be more reliably suppressed.
- the adsorption stabilization energy Ea of the noble metal particles 8 on the anchor particles 9 and the adsorption stabilization energy Eb of the noble metal particles 8 on the enclosure 12 can be calculated by simulation using a density functional method. It can.
- This density functional method is a method for predicting the electronic state of a crystal by introducing a Hamiltonian that incorporates a correlation effect between many electrons. The principle is based on the mathematical theorem that the total energy of the ground state of the system can be expressed by an electron density functional method.
- the density functional method is highly reliable as a method for calculating the electronic state of a crystal.
- Such a density functional method is suitable for predicting an electronic state at the interface between the anchor particle 9 or the inclusion material 12 and the noble metal particle 8.
- the catalyst of the present embodiment which is designed based on a combination of precious metal particles, anchor particles and inclusion materials selected based on actual simulation values, is less prone to coarsening of precious metal particles and has high purification performance even after high temperature durability. Has been confirmed to maintain.
- Analysis software for simulation using such a density functional method is commercially available, and examples of calculation conditions of the analysis software include the following.
- an oxygen storage / release material that is disposed in the vicinity of a noble metal and stores and desorbs active oxygen when the exhaust gas atmosphere changes is an important material for improving the purification performance of the catalyst.
- the amount of OSC material in the catalyst is too small, sufficient active oxygen cannot be supplied to the noble metal in a rich atmosphere, and the purification performance of CO and HC deteriorates. Conversely, if the amount of OSC material is too large, the active oxygen occluded by the OSC material is excessively released and the NOx purification performance deteriorates when the OSC material fluctuates greatly from a lean atmosphere to a stoichiometric or rich atmosphere. Therefore, there is an appropriate value for the amount of OSC material in the catalyst, and such an appropriate value can be obtained from experiments.
- the general amount of OSC material varies depending on the type of noble metal in the catalyst and the amount of noble metal used, but is 5 to 100 g / L in terms of CeO 2 per unit capacity.
- the supply efficiency of active oxygen increases as the distance between the noble metal and the OSC material is shorter. Therefore, when the atmosphere changes, active oxygen can be supplied to the noble metal in a shorter time. Therefore, it is considered that the fact that the distance between the noble metal and the OSC material is close has the same performance improvement effect as (2) the improvement of the oxygen absorption / release rate among the above three conditions.
- the structure in which the noble metal is supported on the OSC material may not always be optimal for the following reasons.
- the OSC material has a large decrease in specific surface area under a high temperature exhaust gas atmosphere as compared with alumina or the like. Therefore, when the noble metal is supported on the OSC material, the specific surface area is likely to decrease due to aggregation of the noble metal.
- rhodium has a high catalytic activity in the reduced state and tends to decrease in the highly oxidized state.
- active oxygen is supplied mainly on the interface of the Rh-OSC material, so that rhodium is in a highly oxidized state, which may cause a decrease in catalyst performance.
- the co-inclusion particle 5 includes a central point of the catalyst unit 13 containing the noble metal particles 8 and the anchor particles 9 and a central point of the promoter unit 14 containing the first promoter particles 11 having oxygen storage / release capability. Is preferably 5 nm to 300 nm. By setting the average distance within this range, it is possible to prevent a decrease in catalyst performance due to an excessive supply of active oxygen while efficiently supplying active oxygen to the noble metal.
- the average distance between the center point of the catalyst unit 13 and the center point of the promoter unit 14 is more preferably 40 nm to 300 nm.
- the distance measurement between the catalyst unit 13 and the promoter unit 14 in the anchor / promoter simultaneous inclusion particles is as follows. (1) TEM-EDX analysis or HAADF-STEM analysis of anchor / promoter simultaneous inclusion particles, (2) Contour extraction of anchor particles and first promoter particles from the image, (3) Set a circle approximation and center point from the surface area based on the extracted contour, (4) Find nearest center point and measure distance, It can be done with the procedure. Note that the distance measurement method is not limited to such a method, and any other method may be used as long as it is an objective and reproducible analysis method.
- TEM-EDX analysis or HAADF analysis of anchor / promoter simultaneous inclusion particles The anchor / promoter simultaneous inclusion particles are embedded in epoxy resin, and after curing, an ultrathin section is prepared with an ultramicrotome. . The section is used to observe the inclusion particles with a transmission electron microscope (TEM) or HAADF-STEM (High-Angle Angular Dark-Field Scanning Transmission Electron Microscopy), the anchor particles and the first promoter particles, Discriminate the inclusion material.
- TEM transmission electron microscope
- HAADF-STEM High-Angle Angular Dark-Field Scanning Transmission Electron Microscopy
- the anchor particles and the first promoter particles may overlap in element type.
- the presence or absence of the noble metal species can be detected by EDX (energy dispersive X-ray analyzer). Can be distinguished from the first promoter particles.
- EDX energy dispersive X-ray analyzer
- the noble metal particle size is smaller than the X-ray beam diameter of EDX, noble metal may not be detected.
- the anchor particles and the first promoter particles contain Ce or Pr as the OSC material, the contents of the anchor particles and the first promoter particles determined in advance and the detection of Ce or Pr are detected. It is preferable to perform discrimination using the intensity ratio. In the case of a HAADF-STEM image, it can be determined by contrast.
- FIG. 5 shows an example of a TEM-EDX photograph of anchor / promoter simultaneous inclusion particles.
- image processing is performed on the photograph obtained using TEM-EDX, and the contours of the particles of the anchor particles 9 and the first promoter particles 11 are extracted.
- the area of each particle is obtained, and a circle having the same area as this area is assumed.
- the first promoter particle 11 (promoter unit 14) closest to the specific anchor particle 9 (catalyst unit 13) is searched, and the center distance of each circle is measured.
- a straight line connecting the anchor particles 9 and the first promoter particles 11 is indicated by a solid line
- a straight line connecting the anchor particles 9 or the first promoter particles 11 is indicated by a broken line.
- the anchor / promoter simultaneous enclosure particles 5 preferably have a degree of dispersion of 40% or more of the catalyst unit 13 and the promoter unit 14 in the enclosure particles.
- the degree of dispersion can be obtained from the following equation 1.
- ⁇ is the standard deviation of the distribution of the center-to-center distance between the catalyst unit 13 and the promoter unit 14 in the co-inclusion particles 5.
- Av. Is the average center-to-center distance between the catalyst unit 13 and the co-catalyst unit 14 in the enclosure particle 5
- FIG. 6 is a graph showing the relationship between the center-to-center distance between the catalyst unit 13 and the promoter unit 14 in the co-inclusion particles 5 and the appearance frequency of the distance.
- the frequency distribution is a normal distribution
- an arbitrary sample is within the range of ⁇ .
- the degree of dispersion is expressed as the probability of entering.
- the standard deviation is ⁇ means that 68.27% of the center-to-center distance between the catalyst unit 13 and the promoter unit 14 is distributed within the average center-to-center distance Av (nm) ⁇ ⁇ (nm).
- FIG. 7 shows a schematic diagram of an example of catalyst powder having a high degree of dispersion (FIG. 7A) and a schematic diagram of an example of catalyst powder having a low degree of dispersion (FIG. 7B).
- the degree of dispersion of the catalyst is 100% (this means that the distance variation is zero). Means).
- the degree of dispersion of the catalyst approaches 0%. That is, when all the distances between the catalyst unit and the promoter unit are geometrically evenly arranged, ⁇ is 0 and the degree of dispersion is 100%.
- the degree of dispersion defined in this way is preferably 40% or more. If the degree of dispersion is 40% or more, the distance between the particles is sufficiently maintained, and the deviation is small, so that aggregation of the compounds after durability is suppressed. In particular, the degree of dispersion is more preferably 50% or more.
- This dispersity is determined in the course of producing the co-inclusion particles 5 between the anchor particles and the first promoter particles immediately before drying the slurry mixed with the anchor particles and the first promoter particles, and further the precursor of the clathrate. There is a correlation with the degree of aggregation. Since the degree of aggregation depends on the stirring force of the slurry, the degree of dispersion can be improved by vigorously stirring the slurry.
- the second promoter particles 6 contained in the catalyst layer 3 are dispersed in the catalyst layer 3 together with the anchor / promoter simultaneous inclusion particles 5 as shown in FIG. And since the 2nd promoter particle 6 is arrange
- the active oxygen occluded by the first promoter particles 11 and the second promoter particles 6 is released, so that the oxidation of HC and CO is also efficient. It can be carried out.
- the ratio of the weight of the first promoter particles to the total weight of the first promoter particles and the second promoter particles is preferably 0.3 or more. More preferably, it is 4 to 0.8.
- excess oxygen can be occluded by the 2nd promoter particle, while the occlusion and discharge
- the second promoter particles 6 preferably contain at least one of cerium (Ce) and praseodymium (Pr) having oxygen storage / release capability, as in the case of the first promoter particles 11.
- the second promoter particles 6 are preferably composed mainly of a compound having a high oxygen storage / release capability, such as cerium oxide (CeO 2 ) or praseodymium oxide (Pr 6 O 11 ).
- the second promoter particles 6, like the first promoter particles 11, are oxidized further containing at least one selected from iron (Fe), manganese (Mn), cobalt (Co), and nickel (Ni). It is preferable that it is a thing. By containing at least one of these transition metals, the catalytic performance, particularly the CO and NO purification rate, can be improved by the active oxygen contained in the transition metal.
- the second promoter particles 6 preferably further include at least one NOx adsorbent selected from barium (Ba), magnesium (Mg), calcium (Ca), strontium (Sr), and sodium (Na). Since any compound containing these elements acts as a NOx adsorbent, the NOx purification performance can be improved.
- NOx adsorbent selected from barium (Ba), magnesium (Mg), calcium (Ca), strontium (Sr), and sodium (Na). Since any compound containing these elements acts as a NOx adsorbent, the NOx purification performance can be improved.
- the anchor / promoter simultaneous inclusion particles 5 and the second promoter particles 6 preferably have an average particle diameter (D50) of 6 ⁇ m or less.
- This average particle diameter is an average particle diameter of the encapsulated particles 5 and the second promoter particles 6 in the catalyst layer 3 as shown in FIG.
- these average particle diameters exceed 6 ⁇ m, the distance from the outer peripheries of the encapsulated particles 5 and the second promoter particles 6 to the center of the particles increases, and the gas diffusibility to the center of the particles is significantly reduced. Therefore, there is a possibility that the purification performance is lowered.
- the thickness exceeds 6 ⁇ m, peeling or unevenness easily occurs when the honeycomb carrier is coated.
- the average particle diameter of the anchor / promoter simultaneous inclusion particles 5 and the second promoter particles 6 is more preferably in the range of 1 ⁇ m to 4 ⁇ m, which can form appropriate interparticle voids and can further suppress peeling.
- the average particle diameter of the anchor / promoter simultaneous inclusion particles 5 and the second promoter particles 6 can be determined by applying a slurry containing these particles to a laser diffraction particle size distribution measuring device.
- an undercoat layer 4 made of a heat-resistant inorganic oxide can be provided in the lowermost layer of the catalyst layer.
- the undercoat layer 4 is mainly disposed at the corner of the cell 2 a of the honeycomb carrier 2.
- the catalytically active component in the catalyst layer coated on the undercoat layer 4 is locally unevenly distributed to the cell angle, and the amount of the catalytically active component to be coated on the cell flat portion (cell wall portion) is reduced. Or the catalyst layer can be prevented from falling off the support.
- alumina or the like can be used as the heat-resistant inorganic oxide in the undercoat layer.
- the manufacturing method of this catalyst has the process of grind
- the noble metal particles 8 are supported on the anchor particles 9.
- the noble metal particles can be supported by an impregnation method.
- the anchor particles 9 carrying the noble metal particles 8 on the surface are pulverized using a bead mill or the like to obtain a desired particle diameter.
- the first promoter particles 11 are also pulverized using a bead mill or the like to obtain a desired particle size.
- the anchor particles 9 and the first promoter particles 11 may be pulverized in a mixed state or individually.
- a crushing process can be skipped by using fine raw materials, such as an oxide colloid, as a raw material of the anchor particle 9 and / or the 1st promoter particle 11.
- the anchor particles and the first promoter particles are clathrated with the clathrate, the clathrated anchor particles and the first promoter particles are not mixed.
- the anchor particles and the first promoter particles are preferably clathrated simultaneously with the clathrate. Thereby, the anchor particles and the first promoter particles can be dispersed uniformly and without unevenness.
- the anchor particles and the first promoter particles are put into a slurry in which a clad material precursor is dispersed and stirred.
- a clad material precursor is dispersed and stirred.
- the precursor of the inclusion material adheres around the anchor particles 9 and the first promoter particles 11.
- each particle is dispersed in the slurry, and as a result, the degree of dispersion can be improved.
- the mixed slurry can be dried and fired to obtain the encapsulated particles 5 in which the inclusion material is formed around the anchor particles 9 and the first promoter particles 11.
- the anchor / promoter simultaneous inclusion particles and the second promoter particles are mixed and pulverized.
- This pulverization may be wet or dry, but usually the anchor / promoter simultaneous inclusion particles and the second promoter particles are mixed in a solvent such as ion-exchanged water and stirred, and then pulverized using a ball mill or the like, A catalyst slurry is obtained.
- a binder is added to the catalyst slurry as necessary.
- the average particle diameter (D50) of the anchor / promoter simultaneous inclusion particles and the second promoter particles in the catalyst slurry is preferably 6 ⁇ m or less as described above.
- the catalyst slurry is applied to the inner surface of the honeycomb carrier, dried and fired, whereby an exhaust gas purifying catalyst can be obtained.
- the exhaust gas purification system 20 of the present embodiment has a three-way catalyst 23 arranged upstream of the exhaust gas passage 22 of the internal combustion engine 21, and the exhaust gas purification system of the present embodiment downstream thereof. It can be set as the structure which has arrange
- the three-way catalyst 23 can be activated early and the exhaust gas can be purified even in a low temperature range. Further, even when the three-way catalyst 23 cannot completely purify NOx, the exhaust gas purifying catalyst 1 provided on the downstream side of the three-way catalyst 23 has extremely high NOx purifying performance, so that NOx is finally purified with high efficiency. be able to.
- the exhaust gas purification system of this invention is not restricted to the structure shown in FIG. For example, a three-way catalyst or a NOx adsorption catalyst may be further provided before and after the exhaust gas purification catalyst 1. Further, the exhaust gas-purifying catalyst 1 of the present invention can be used for various internal combustion engines such as gasoline engines, lean burn engines, direct injection engines, and diesel engines.
- Example 1 Co-inclusion particle preparation
- An aqueous rhodium nitrate solution was impregnated with a ZrLa composite oxide (anchor material), dried at 150 ° C. for 12 hours, and then fired at 400 ° C. for 1 hour to obtain an Rh-supported ZrLa composite oxide powder.
- the Rh-containing anchor material slurry was obtained by putting into pure water so that the solid content of the powder was 40% and pulverizing with a bead mill.
- Table 1 shows the average secondary particle diameter (D50) of the anchor material (ZrLa composite oxide) in the Rh-containing anchor material slurry. The average secondary particle diameter was measured using a laser diffraction / scattering particle size distribution analyzer LA-920 manufactured by Horiba, Ltd.
- the first promoter particle slurry is obtained by charging the ZrCeNd composite oxide (first promoter particles) into pure water so as to have a solid content of 40% and pulverizing with a bead mill. It was.
- Table 1 shows the average secondary particle diameter (D50) of the first promoter particles (ZrCeNd composite oxide) in the first promoter particle slurry.
- the obtained slurry was put into a cordierite honeycomb carrier ( ⁇ 110 mm, capacity 0.92 L, 4 mil / 600 cpsi), excess slurry was removed with an air flow, and air-dried at 120 ° C. Subsequently, the undercoat layer was formed by baking at 400 degreeC in the air for 1 hour. At this time, the coating amount of the undercoat layer per liter of the honeycomb carrier was 50 g / L.
- the clathrate inclusion particles-second promoter-containing slurry was applied to the honeycomb carrier on which the Pt-containing catalyst layer was formed, dried and fired.
- an Rh-containing catalyst layer of 100 g / L per 1 L of honeycomb was formed.
- the Rh content per liter of the honeycomb was 0.06 g / L.
- Table 1 shows the ratio between the total weight of the anchor material and the first promoter particles and the weight of the clathrate.
- Example 2 Except that the content was changed so that the ratio of the weight of the first promoter particles to the total weight of the first promoter particles and the second promoter particles was as shown in Table 1, it was the same as in Example 1. The catalyst of Example 2 was obtained.
- Example 3 The same procedure as in Example 1 was conducted except that the bead mill conditions were changed so that the average secondary particle diameter (D50) of the first promoter particles (ZrCeNd composite oxide) in the co-inclusion particles became the value shown in Table 1. Thus, the catalyst of Example 3 was obtained.
- Example 4 A catalyst of this example was obtained in the same manner as in Example 1 except that as the cordierite honeycomb carrier, ⁇ 36 mm, capacity 0.12 L, 4 mil / 600 cpsi was used.
- Examples 5 to 9 and 12 to 14 The first and second promoter particles in Example 1 have the material compositions shown in Tables 2 and 3, respectively, and the average secondary particle diameter (D50) of the anchor particles and the first promoter particles is shown in Tables 2 and 3.
- the catalysts of Examples 5 to 9 and 12 to 14 were obtained in the same manner as Example 1 except that the honeycomb carrier of Example 4 was used.
- Example 10 In Example 1, the co-clathing particles and the second promoter particles in the slurry were adjusted by adjusting the shaking of the magnetic alumina pot when preparing the surface-coated co-clathing particles-second promoter-containing slurry.
- the catalyst of Example 10 was obtained in the same manner as in Example 1 except that the particle diameter of was changed to 7.0 ⁇ m and the honeycomb carrier of Example 4 was used.
- Example 11 The catalyst of Example 11 was obtained in the same manner as in Example 1 except that the dispersity was set to the values shown in Table 2 with respect to Example 1 and the honeycomb carrier of Example 4 was used. These values can be achieved by weakening the stirring force when mixing the Rh-containing anchor material slurry, the first promoter particle slurry, and the boehmite slurry in the above-mentioned simultaneous inclusion particle preparation step.
- Example 15 The catalyst of Example 15 was obtained in the same manner as in Example 1 except that the anchor material in Example 1 had the material composition shown in Table 3 and the honeycomb carrier of Example 4 was used.
- Example 16 to 19 Catalysts of Examples 16 to 19 were obtained in the same manner as in Example 1 except that the clathrate in Example 1 had the material composition shown in Table 3 and the honeycomb carrier of Example 4 was used. At this time, the amount of Ba, Mg, La and Na added to alumina is 5 weight percent as an oxide.
- Example 1 In the same manner as in Example 1, an inner layer and an intermediate layer were formed on the honeycomb carrier.
- the clathrate-containing slurry was applied to the honeycomb carrier on which the Pt-containing catalyst layer was formed, dried and fired.
- an Rh-containing catalyst layer having 100 g / L per 1 L of honeycomb was formed.
- the Rh content per liter of the honeycomb was 0.06 g / L.
- the addition amount of the 1st promoter particle was adjusted so that the total amount of the promoter particle contained in a surface layer might become the same as Example 1.
- the comparative example 1 is an example which does not contain a 2nd promoter particle.
- Rh powder preparation (1) An aqueous rhodium nitrate solution was impregnated with a ZrLa composite oxide (anchor material), dried at 150 ° C. for 12 hours, and then fired at 400 ° C. for 1 hour to obtain an Rh-supported ZrLa composite oxide powder. Next, the Rh-containing anchor material slurry was obtained by putting into pure water so that the solid content of the powder was 40% and pulverizing with a bead mill. Table 1 shows the average secondary particle diameter (D50) of the ZrLa composite oxide in the Rh-containing anchor material slurry.
- D50 average secondary particle diameter
- Pt powder preparation A Pt catalyst powder was obtained in the same manner as in Example 1.
- Example 2 In the same manner as in Example 1, an inner layer and an intermediate layer were formed on the honeycomb carrier.
- the clathrate powder-second promoter-containing slurry was applied to the honeycomb carrier on which the Pt-containing catalyst layer was formed, dried and fired.
- an Rh-containing catalyst layer having 100 g / L per 1 L of honeycomb was formed.
- the Rh content per liter of the honeycomb was 0.06 g / L.
- the addition amount of the 2nd promoter particle was adjusted so that the total amount of the promoter particle contained in a surface layer might become the same as Example 1.
- the comparative example 2 is an example which does not contain the 1st promoter particle.
- Comparative Example 3 A catalyst of Comparative Example 3 was obtained in the same manner as in Example 1 except that the first and second promoter particles were not added to Example 1 and the honeycomb carrier of Example 4 was further used.
- Table 4 shows the content of each element in the composite oxide used in Examples 1 to 19 and Comparative Examples 1 to 3.
- the distance between the catalyst unit (anchor particles) and the promoter unit (first promoter particles) in each catalyst was measured with a TEM-EDX analyzer (HF-2000 manufactured by Hitachi, Ltd.). The acceleration voltage at this time was 200 kV. Moreover, the cutting conditions by the ultra microtome were normal temperature. Then, the contours of the anchor particles and the first promoter particles were extracted from the image obtained from the TEM-EDX analyzer using an image analyzer (KS-400 manufactured by Carl Zeiss Co., Ltd.). After that, the area was calculated based on the extracted contour, the circle approximation and the center point were set, the nearest center point was searched and the distance was measured, and the distance between the catalyst unit and the promoter unit was obtained. .
- Equation 1 shows the degree of dispersion of the catalyst.
- Table 1 shows the center-to-center distance between the promoter unit and the promoter unit in Examples 1 to 3 and Comparative Examples 1 and 2, the degree of dispersion, and the NOx residual ratio.
- Examples 12 to 19 were subjected to endurance treatment and then examined for NOx conversion.
- a catalyst was attached to the exhaust system of a 3500 cc gasoline engine, the catalyst inlet temperature was set to 700 ° C., and the system was operated for 50 hours. Unleaded gasoline was used as the fuel.
- NOx conversion first, the catalyst of the example after the endurance treatment was arranged in the exhaust system of a 2000 cc gasoline engine. Next, a 40-second lean atmosphere (A / F: 25) and a 2-second rich atmosphere (A / F: 11) were repeated, and the engine was operated so that the catalyst inlet temperature was 300 to 350 ° C. From the NOx concentration at the inlet and outlet of the catalyst, the NOx conversion rate was obtained from Equation 3.
- the surface layers of Examples 1 and 2 contain both anchor / promoter simultaneous inclusion particles and second promoter particles. And the surface layer of the comparative example 1 does not contain the 2nd promoter particle, and the comparative example 2 does not contain the 1st promoter particle.
- 9 shows the NOx residual ratios of Examples 1 and 2 and Comparative Examples 1 and 2, Examples 1 and 2 containing both the first and second promoter particles are comparative examples. Compared with 1 and 2, the NOx residual rate is lower. This is presumed to be because the addition of the second promoter particles makes it difficult for excess oxygen to reach the deep part of the catalyst layer, so that the NOx purification ability in the surface layer and the middle layer is improved. Further, from FIG. 9, when the weight ratio of the first promoter particles to the total weight of the first promoter particles and the second promoter particles is particularly 0.4 to 0.8, the NOx residual ratio is remarkably reduced. You can see that
- the NOx residual rate decreases as the average secondary particle diameter of the first promoter particles decreases. This is presumably because the surface area of the first promoter particles is greatly improved and the supply rate of active oxygen is improved.
- the first and second promoter particles were added, and a transition metal was added to the first and second promoter particles, thereby achieving an extremely high NOx purification rate. can do.
- the average particle diameter (D50) of the anchor / promoter simultaneous inclusion particles and the second promoter particles exceeds 6 ⁇ m, the NOx conversion rate slightly decreases, so the average particle diameter Is preferably 6 ⁇ m or less.
- the degree of dispersion is preferably 40% or more.
- the NOx adsorbent is contained in the anchor material, the first and second promoter particles, and the clathrate, so that a high NOx conversion rate is exhibited.
- a ZrLa composite oxide (anchor particles) having a specific surface area of about 70 m 2 / g was impregnated in an aqueous rhodium nitrate solution, dried overnight at 150 ° C. and then fired at 400 ° C. for 1 hour to carry 1.0 wt% Rh.
- Anchor particles were obtained.
- the anchor particles carrying Rh were pulverized by a bead mill to obtain an average secondary particle diameter (D50) shown in Table 5.
- ZrCe composite oxide (first promoter particles) having a specific surface area of 80 m 2 / g was pulverized by a bead mill to obtain an average secondary particle size (D50) shown in Table 5.
- boehmite as a precursor of the inclusion material, nitric acid, and pure water were mixed and stirred for 1 hour.
- the ground anchor particles and the first promoter particles were slowly put into the liquid after stirring, and the mixture was further stirred for 2 hours using a high-speed stirrer.
- this liquid mixture was rapidly dried and further dried at 150 ° C. for a whole day and night to remove moisture. Further, this was calcined in the air at 550 ° C. for 3 hours to obtain anchor / promoter simultaneous inclusion particles of Reference Example 1.
- a catalyst powder was prepared by previously mixing Pt-supported Al 2 O 3 powder and Ce—Zr—O x powder. And it slurryed similarly to the said enclosure particle
- Reference Example 2 uses a colloidal solution with a primary particle size of 21 nm as anchor particles (ZrCe composite oxide) and a colloidal solution with a primary particle size of 65 nm as first promoter particles (ZrCe composite oxide). Only Rh was supported. Then, the catalyst of this reference example was obtained in the same manner as in Reference Example 1 except that the step of pulverizing anchor particles carrying Rh was omitted and the anchor particles, the first promoter particles and the boehmite slurry were mixed.
- Comparative Example 4 is an example in which the anchor particles and the first promoter particles are not covered simultaneously with the inclusion material but are covered separately.
- a rhodium nitrate solution was impregnated with a ZrLa composite oxide (anchor particles) having a specific surface area of about 70 m 2 / g, dried at 150 ° C. for a whole day and night, and then fired at 400 ° C. for 1 hour to carry 1.0 wt% of Rh.
- Anchor particles were obtained.
- the anchor particles carrying Rh were pulverized by a bead mill to obtain an average secondary particle diameter (D50) shown in Table 5.
- boehmite as a precursor of the inclusion material, nitric acid, and pure water were mixed and stirred for 1 hour.
- the pulverized Rh-supported anchor particles were slowly put into the liquid after stirring, and further stirred for 2 hours using a high-speed stirrer.
- this liquid mixture was rapidly dried and further dried at 150 ° C. for a whole day and night to remove moisture. Furthermore, this was baked in the air at 550 degreeC for 3 hours, and the anchor particle inclusion powder was obtained.
- the ZrCe composite oxide (first promoter particles) was pulverized to obtain an average secondary particle size (D50) described in Table 5. Furthermore, boehmite as a precursor of the inclusion material, nitric acid, and pure water were mixed and stirred for 1 hour. Then, the pulverized first promoter particles were slowly put into the liquid after stirring, and further stirred for 2 hours using a high-speed stirrer. Then, this liquid mixture was rapidly dried and further dried at 150 ° C. for a whole day and night to remove moisture. Furthermore, this was baked in the air at 550 degreeC for 3 hours, and the 1st promoter particle inclusion powder was obtained.
- D50 average secondary particle size
- a honeycomb carrier coated with 100 g / L of Pt-supported Al 2 O 3 powder and Ce—Zr—O x powder was prepared in the same manner as in Reference Example 1 above. Then, the above Rh catalyst slurry was adhered onto the honeycomb carrier coated with Pt, excess slurry in the cell was removed with an air flow, dried at 130 ° C., and then fired at 400 ° C. for 1 hour. As a result, a catalyst coated with 50 g / L of the catalyst layer containing the anchor / promoter inclusion powder was obtained.
- Comparative Example 5 is an example in which the first promoter particles are not included and the noble metal is supported on anchor particles having oxygen storage / release capability.
- a rhodium nitrate solution was impregnated with a ZrCe composite oxide (anchor particles) having a specific surface area of about 70 m 2 / g, dried at 150 ° C. for a whole day and night, and then fired at 400 ° C. for 1 hour to carry 1.0 wt% Rh.
- Anchor particles were obtained.
- the anchor particles carrying Rh were pulverized to obtain the average secondary particle diameter (D50) shown in Table 5.
- boehmite as a precursor of the inclusion material, nitric acid, and pure water were mixed and stirred for 1 hour.
- pulverization were thrown into the liquid after this stirring slowly, and also it stirred for 2 hours using the high-speed stirrer.
- this liquid mixture was rapidly dried and further dried at 150 ° C. for a whole day and night to remove moisture. Furthermore, this was baked in the air at 550 degreeC for 3 hours, and the anchor particle inclusion powder of the comparative example 5 was obtained.
- a honeycomb carrier coated with 100 g / L of Pt-supported Al 2 O 3 powder and Ce—Zr—O x powder was prepared in the same manner as in Reference Example 1 above. Then, the above Rh catalyst slurry was adhered onto the honeycomb carrier coated with Pt, excess slurry in the cell was removed with an air flow, dried at 130 ° C., and then fired at 400 ° C. for 1 hour. As a result, a catalyst coated with 50 g / L of a catalyst layer containing anchor particle inclusion powder was obtained.
- the average center-to-center distance between the catalyst unit and the promoter unit in Reference Examples 1 and 2 and Comparative Examples 4 and 5 was determined in the same manner as in the above example, and the relationship between the average center-to-center distance and the NOx conversion rate 10 shows.
- FIG. 10 shows that when the center-to-center distance between these particles is 5 nm to 300 nm, the NOx conversion rate is 90% or more, and high NOx purification performance can be exhibited. Further, from FIG. 10 and Examples 1 to 19, it can be seen that if the average center distance between the catalyst unit and the promoter unit is 150 nm to 250 nm, extremely high NOx purification performance can be exhibited.
- the present invention has been described with reference to the examples, comparative examples, and reference examples, the present invention is not limited to these, and various modifications are possible within the scope of the gist of the present invention.
- the catalyst layer may be a single layer or three or more layers.
- high NOx purification performance can be exhibited without providing the undercoat layer 4 shown in FIG.
- promoter particles having an oxygen storage / release capability are disposed between pores formed by anchor / promoter simultaneous inclusion particles. Therefore, even when the air-fuel ratio of the exhaust gas fluctuates, excess oxygen can be occluded and high NOx purification performance can be exhibited even inside the catalyst layer.
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Abstract
Description
図1では、本発明の実施形態に係る排ガス浄化用触媒(以下、触媒ともいう。)1を示す。排ガス浄化用触媒1は、図1(a)に示すように、複数のセル2aを有するハニカム担体(耐火性無機担体)2を備えている。排気ガスは、排気ガス流通方向Fに沿って各セル2a内を流通し、そこで触媒層と接触することにより浄化される。
上記アンカー・助触媒共包接粒子5(以下、共包接粒子5ともいう。)は、図1(d)に示すように、貴金属粒子8と、アンカー粒子9と、第一助触媒粒子11とを含有している。上記アンカー粒子9は、貴金属粒子8のアンカー材として貴金属粒子8を表面に担持している。また、上記第一助触媒粒子11は、貴金属粒子8と非接触に配設され、酸素吸蔵放出能を有している。さらに共包接粒子5は、貴金属粒子8とアンカー粒子9との複合粒子10及び第一助触媒粒子11を共に包接し、複合粒子10と第一助触媒粒子11を互いに隔てる包接材12を含有する。
(1)アンカー・助触媒共包接粒子のTEM-EDX分析又はHAADF-STEM分析、
(2)画像からのアンカー粒子及び第一助触媒粒子の輪郭抽出、
(3)抽出した輪郭を基に表面積から円近似及び中心点を設定、
(4)最近接中心点の検索と距離測定、
の手順で行うことができる。なお、上記距離測定方法はこのような方法に限られず、他の方法であっても客観的かつ再現性が得られる分析方法であれば良い。
アンカー・助触媒共包接粒子をエポキシ樹脂にて包埋処理し、硬化後、ウルトラミクロトームにより超薄切片を作成する。その切片を用いて、透過型電子顕微鏡(TEM)又はHAADF-STEM(High-Angle Annular Dark-Field Scanning Transmission Electron Microscopy)により共包接粒子を観察し、アンカー粒子及び第一助触媒粒子、更には包接材の判別を行う。具体例として、TEM-EDXを用いた場合の分析条件を説明すると、まず、得られた映像の中でコントラスト(影)の部分に焦点を当て、その部分の元素種を分析し、その元素を含む化合物粒子を特定する。
上記(1)の分析で得られた像よりアンカー粒子及び第一助触媒粒子の輪郭を抽出する。抽出方法は画像処理ソフトを用い、コントラストにより自動で抽出しても良い。また、画像をOHPシートなどに写し取って、手動で抽出しても良い。
これら(3)及び(4)の手順については、いずれも市販の画像処理ソフトにより行うことができる。つまり、抽出した輪郭によりアンカー粒子及び第一助触媒粒子の面積を算出し、その面積と同じ面積の円を仮定する。そして、特定のアンカー粒子に最も近接している第一助触媒粒子を検索し、それぞれの円の中心距離を測定することにより、粒子間距離を求めることができる。
上記触媒層3に含有される第二助触媒粒子6は、図1(c)に示すように、アンカー・助触媒共包接粒子5と共に触媒層3内に分散されている。そして、第二助触媒粒子6は、複数の共包接粒子5の間に形成される細孔5aの中に配置されているため、この細孔内を通過する排気ガス中の酸素を効率的に吸蔵することができる。このため、触媒層の深部まで酸素が到達しにくくなることから、触媒粉末の周囲には酸素が過剰に存在し難くなり、窒素酸化物の還元が効率的に行われるようになる。また、リーン雰囲気からストイキあるいはリッチ雰囲気へと大きく変動する際には、第一助触媒粒子11及び第二助触媒粒子6が吸蔵した活性酸素を放出するため、HC、COの酸化も効率的に行うことができる。
次に、本発明の実施形態にかかる排ガス浄化用触媒の製造方法について説明する。本触媒の製造方法は、上記貴金属粒子とアンカー粒子との複合粒子及び第一助触媒粒子を、個別に又は一体的に粉砕する工程を有する。さらに、粉砕された上記複合粒子及び第一助触媒粒子を、包接材の前駆体を含有したスラリに混合し、乾燥することにより、アンカー・助触媒共包接粒子を調製する工程を有する。また、アンカー・助触媒共包接粒子と、第二助触媒粒子とを混合し、粉砕する工程を有する。
本実施形態の排ガス浄化システム20は、図8に示すように、内燃機関21の排気ガス流路22の上流側に、三元触媒23を配置し、その下流側に本実施形態の排ガス浄化用触媒1を配置した構成とすることができる。また、三元触媒23は、エキゾーストマニホールド24の直下に設けることにより、早期に活性化することができる。
(共包接粒子調製)
(1)硝酸ロジウム水溶液にZrLa複合酸化物(アンカー材)を含浸し、150℃で12時間乾燥した後、400℃で1時間焼成することにより、Rh担持ZrLa複合酸化物粉末を得た。次に、この粉末に対し固形分が40%となるように純水に投入し、ビーズミルにて粉砕することにより、Rh含有アンカー材スラリを得た。Rh含有アンカー材スラリ中のアンカー材(ZrLa複合酸化物)の平均二次粒子径(D50)を表1に記載した。なお、この平均二次粒子径の測定には、株式会社堀場製作所製レーザ回折/散乱式粒度分布測定装置LA-920を用いた。
(1)ジニトロジアミン白金水溶液にCeZr複合酸化物を含浸し、150℃で12時間乾燥した後、400℃で1時間焼成することにより、Pt担持CeZr複合酸化物粉末を得た。次に、この粉末に対し固形分が40%となるように純水に投入し、ビーズミルにて粉砕することにより、Pt担持CeZr複合酸化物スラリを得た。
(1)内層コート
Al2O3粉末と、Al2O3粉末に対して8質量%のベーマイトと、硝酸水溶液とを磁性アルミナポットに投入した。さらに、上記磁性アルミナポットにアルミナボールを投入した後、振とうすることにより、貴金属成分を含有しないスラリを得た。
上記内層コートと同様に上記Pt触媒粉末のスラリを調製した。次に、上記内層コートと同様に、Pt触媒粉末のスラリをアンダーコート層が形成されたハニカム担体に塗布し、乾燥及び焼成した。これにより、ハニカム担体1Lあたり60g/LのPt含有触媒層を形成した。なお、この時のハニカム担体1LあたりのPt含有量は0.29g/Lであった。
上記共包接粒子と、ZrCeNd複合酸化物粉末(第二助触媒粒子)と、共包接粒子及びZrCeNd複合酸化物粉末に対して8質量%のベーマイトと、硝酸水溶液とを磁性アルミナポットに投入した。さらに、上記磁性アルミナポットにアルミナボールを投入した後、振とうすることにより、共包接粒子-第二助触媒含有スラリを得た。このとき、第一助触媒粒子及び第二助触媒粒子の総重量に対する第一助触媒粒子の重量の比率は、表1に記載のとおりとなるようにした。また、共包接粒子-第二助触媒含有スラリ中における共包接粒子及び第二助触媒粒子の平均粒子径(D50)も、表1に記載した(表中の触媒粉末粒径参照)。
第一助触媒粒子及び第二助触媒粒子の総重量に対する第一助触媒粒子の重量の比率が、表1に記載のとおりとなるように含有量を変えた以外は実施例1と同様にして、実施例2の触媒を得た。
共包接粒子中の第一助触媒粒子(ZrCeNd複合酸化物)の平均二次粒子径(D50)が表1中の値となるようにビーズミルの条件を変更した以外は実施例1と同様にして、実施例3の触媒を得た。
コージェライト製ハニカム担体として、φ36mm,容量0.12L,4mil/600cpsiを使用した以外は実施例1と同様にして、本実施例の触媒を得た。
実施例1における第一及び第二助触媒粒子をそれぞれ表2及び表3中の材料組成とし、さらにアンカー粒子及び第一助触媒粒子の平均二次粒子径(D50)を表2及び表3中の粒子径とし、さらに実施例4のハニカム担体を使用した以外は、実施例1と同様にして、実施例5~9及び12~14の触媒を得た。
実施例1において、表層コートの共包接粒子-第二助触媒含有スラリを調製する際、磁性アルミナポットの振とうを調節することにより、上記スラリ中における共包接粒子及び第二助触媒粒子の粒子径を7.0μmとし、さらに実施例4のハニカム担体を使用した以外は、実施例1と同様にして、実施例10の触媒を得た。
実施例1に対して分散度を表2の値とし、さらに実施例4のハニカム担体を使用した以外は実施例1と同様にして、実施例11の触媒を得た。なお、これらの値は、上記共包接粒子調製工程における、Rh含有アンカー材スラリと、第一助触媒粒子スラリと、ベーマイトスラリとを混合する際の攪拌力を弱めることにより成し得る。
実施例1におけるアンカー材を表3の材料組成とし、さらに実施例4のハニカム担体を使用した以外は実施例1と同様にして、実施例15の触媒を得た。
実施例1における包接材を表3の材料組成とし、さらに実施例4のハニカム担体を使用した以外は実施例1と同様にして、実施例16~19の触媒を得た。なお、この際アルミナに対するBa,Mg,La及びNaの添加量は、酸化物として5重量パーセントである。
(共包接粒子調製及びPt粉末調製)
実施例1と同様の方法で、共包接粒子及びPt触媒粉末を得た。
まず、上記共包接粒子と、共包接粒子に対して8質量%のベーマイトと、硝酸水溶液とを磁性アルミナポットに投入した。さらに、磁性アルミナポットにアルミナボールを投入した後、振とうすることにより、共包接粒子含有スラリを得た。共包接粒子含有スラリ中における共包接粒子の平均粒子径(D50)を表1に記載した(表中の触媒粉末粒径参照)。
(Rh粉末調製)
(1)硝酸ロジウム水溶液にZrLa複合酸化物(アンカー材)を含浸し、150℃で12時間乾燥した後、400℃で1時間焼成することにより、Rh担持ZrLa複合酸化物粉末を得た。次に、この粉末に対し固形分が40%となるように純水に投入し、ビーズミルにて粉砕することにより、Rh含有アンカー材スラリを得た。Rh含有アンカー材スラリ中のZrLa複合酸化物の平均二次粒子径(D50)を表1に記載した。
実施例1と同様にPt触媒粉末を得た。
まず、上記包接粉末と、ZrCeNd複合酸化物粉末(第二助触媒粒子)と、包接粉末及びZrCeNd複合酸化物粉末に対して8%のベーマイトと、硝酸水溶液とを磁性アルミナポットに投入した。さらに、磁性アルミナポットにアルミナボールを投入した後、振とうすることにより、包接粉末-第二助触媒含有スラリを得た。包接粉末-第二助触媒含有スラリ中における包接粉末及び第二助触媒粒子の粒子径を、表1に記載した(表中の触媒粉末粒径参照)。
実施例1に対して第一及び第二助触媒粒子を添加せず、さらにさらに実施例4のハニカム担体を使用した以外は実施例1と同様にして、比較例3の触媒を得た。
実施例1~3及び比較例1,2の触媒について耐久処理を施した後、NOx残存率を調べた。耐久処理の方法は、排気量3500ccのガソリンエンジンの排気系に実施例及び比較例の触媒を装着した後、触媒内部温度を880℃とし、200時間運転した。使用燃料には無鉛ガソリンを使用した。また、NOx残存率は、まず排気量1500ccのガソリンエンジンのエキゾーストマニホールド直下に三元触媒を配置し、さらに上記三元触媒の下流側(床下位置)に耐久処理後の実施例及び比較例の触媒を配置した。次に、エンジンをJC08モードで運転し、実施例及び比較例の触媒の入口及び出口のNOx濃度から、次式2よりNOx残存率を求めた。
実施例4~11及び比較例3について、耐久処理を施した後、NOx転化率を調べた。耐久処理の方法は、排気量3500ccのガソリンエンジンの排気系に触媒を装着した後、触媒入口温度を820℃とし、50時間運転した。使用燃料には無鉛ガソリンを使用した。また、NOx転化率は、まず排気量2400ccのガソリンエンジンの排気系に耐久処理後の実施例及び比較例の触媒を配置した。次に、触媒入口温度が400℃となるようにエンジンを運転し、実施例及び比較例の触媒の入口及び出口のNOx濃度から、次式3よりNOx転化率を求めた。
実施例12~19について、耐久処理を施した後、NOx転化率を調べた。耐久処理の方法は、排気量3500ccのガソリンエンジンの排気系に触媒を装着し、触媒入口温度を700℃とし、50時間運転した。使用燃料には無鉛ガソリンを使用した。また、NOx転化率は、まず排気量2000ccのガソリンエンジンの排気系に耐久処理後の実施例の触媒を配置した。次に、40秒間のリーン雰囲気(A/F:25)と2秒間のリッチ雰囲気(A/F:11)を繰り返し、触媒入口温度が300~350℃となるようにエンジンを運転し、実施例の触媒の入口及び出口のNOx濃度から、式3よりNOx転化率を求めた。
まず、比表面積約70m2/gのZrLa複合酸化物(アンカー粒子)を硝酸ロジウム水溶液に含浸し、150℃で一昼夜乾燥後、400℃で1時間焼成して、Rhを1.0wt%担持したアンカー粒子を得た。このRhを担持したアンカー粒子をビーズミルで粉砕し、表5中に記載の平均二次粒子径(D50)とした。その一方で、比表面積80m2/gのZrCe複合酸化物(第一助触媒粒子)をビーズミルで粉砕し、表5中に記載の平均二次粒子径(D50)とした。
参考例2は、アンカー粒子(ZrCe複合酸化物)に一次粒径が21nmのコロイド溶液を用い、第一助触媒粒子(ZrCe複合酸化物)に一次粒径が65nmのコロイド溶液を用い、アンカー粒子のみにRhを担持させた。そして、Rhを担持させたアンカー粒子の粉砕工程を省き、アンカー粒子及び第一助触媒粒子とベーマイトスラリとを混合した以外は参考例1と同様にして、本参考例の触媒を得た。
比較例4は、アンカー粒子と第一助触媒粒子とを包接材で同時に覆うのではなく、別々に覆った例である。
比較例5は、第一助触媒粒子を有しておらず、貴金属が酸素吸蔵放出能を有するアンカー粒子に担持されている例である。
参考例1,2及び比較例4,5について、耐久処理を施した後、NOx転化率を調べた。耐久処理の方法は、排気量3500ccのガソリンエンジンの排気系に触媒を装着し、触媒入口温度を800℃とし、50時間運転した。使用燃料には無鉛ガソリンを使用した。また、NOx転化率は、まず排気量3500ccのガソリンエンジンの排気系に耐久処理後の参考例及び比較例の触媒を配置した。次に、触媒温度が400℃となるようにエンジンを運転し、参考例及び比較例の触媒の入口及び出口のNOx濃度から、式3よりNOx転化率を求めた。
5 アンカー・助触媒共包接粒子
6 第二助触媒粒子
8 貴金属粒子
9 アンカー粒子
11 第一助触媒粒子
12 包接材
13 触媒ユニット
14 助触媒ユニット
20 排ガス浄化システム
Claims (17)
- 貴金属粒子と前記貴金属粒子のアンカー材として貴金属粒子を担持するアンカー粒子とを含む触媒ユニットと、前記貴金属粒子と非接触に配設され、酸素吸蔵放出能を有する第一助触媒粒子を含む助触媒ユニットと、前記触媒ユニット及び前記助触媒ユニットを共に内包し、かつ、前記触媒ユニットにおける貴金属粒子及びアンカー粒子と前記助触媒ユニットにおける第一助触媒粒子とを互いに隔てる包接材と、を含有するアンカー・助触媒共包接粒子と、
酸素吸蔵放出能を有し、前記包接材によって前記アンカー・助触媒共包接粒子中に内包されない第二助触媒粒子と、
を含有することを特徴とする排ガス浄化用触媒。 - 貴金属粒子と前記貴金属粒子のアンカー材として貴金属粒子を担持するアンカー粒子とを含む触媒ユニットと、前記貴金属粒子と非接触に配設され、酸素吸蔵放出能を有する第一助触媒粒子を含む助触媒ユニットと、前記触媒ユニット及び前記助触媒ユニットを共に内包し、かつ、前記触媒ユニットにおける貴金属粒子及びアンカー粒子と前記助触媒ユニットにおける第一助触媒粒子とを互いに隔てる包接材と、を含有する複数のアンカー・助触媒共包接粒子と、
酸素吸蔵放出能を有し、前記包接材によって前記アンカー・助触媒共包接粒子中に内包されない第二助触媒粒子と、
を含有し、
前記第二助触媒粒子は、複数の前記アンカー・助触媒共包接粒子の間に形成される細孔の中に配置されていることを特徴とする排ガス浄化用触媒。 - 前記第一助触媒粒子及び第二助触媒粒子の総重量に対する第一助触媒粒子の重量の比は、0.3以上であることを特徴とする請求項1又は2に記載の排ガス浄化用触媒。
- 前記触媒ユニットの中心点と前記助触媒ユニットの中心点との間の平均距離は、5nm~300nmであることを特徴とする請求項1乃至3のいずれか一項に記載の排ガス浄化用触媒。
- 前記包接材は、当該包接材により隔てられた区画内に前記助触媒ユニットを含み、かつ、前記助触媒ユニットの平均粒子径Dcと、前記包接材に形成されている細孔の平均細孔径DbとがDb<Dcであって、前記助触媒ユニットにおける第一助触媒粒子が区画を超えて他の区画の第一助触媒粒子と接触し凝集することを抑制することを特徴とする請求項1乃至4のいずれか一項に記載の排ガス浄化用触媒。
- 前記アンカー・助触媒共包接粒子及び前記第二助触媒粒子の平均粒子径は、6μm以下であることを特徴とする請求項1乃至5のいずれか一項に記載の排ガス浄化用触媒。
- 前記貴金属粒子はロジウムを含有し、前記アンカー粒子はジルコニアを含有することを特徴とする請求項1乃至6のいずれか一項に記載の排ガス浄化用触媒。
- 前記第一助触媒粒子及び第二助触媒粒子は、セリウム(Ce)及びプラセオジム(Pr)の少なくともいずれか一方を含有することを特徴とする請求項1乃至7のいずれか一項に記載の排ガス浄化用触媒。
- 前記包接材は、アルミナ及びシリカの少なくともいずれか一方を含有することを特徴とする請求項1乃至8のいずれか一項に記載の排ガス浄化用触媒。
- 前記アンカー・助触媒共包接粒子中における触媒ユニット及び助触媒ユニットの分散度は、40%以上であることを特徴とする請求項1乃至9のいずれか一項に記載の排ガス浄化用触媒。
- 前記アンカー材、第一助触媒粒子及び第二助触媒粒子は、鉄(Fe)、マンガン(Mn)、コバルト(Co)及びニッケル(Ni)の少なくともいずれか一つを含有する酸化物であることを特徴とする請求項1乃至10のいずれか一項に記載の排ガス浄化用触媒。
- 前記アンカー材、第一助触媒粒子及び第二助触媒粒子は、バリウム(Ba)、マグネシウム(Mg)、カルシウム(Ca)、ストロンチウム(Sr)及びナトリウム(Na)の少なくともいずれか一つを含有する酸化物であることを特徴とする請求項1乃至11のいずれか一項に記載の排ガス浄化用触媒。
- 前記包接材は、セリウム(Ce)、ジルコニウム(Zr)、ランタン(La)、バリウム(Ba)、マグネシウム(Mg)、カルシウム(Ca)、ストロンチウム(Sr)、ナトリウム(Na)の少なくともいずれか一つを含有する酸化物であることを特徴とする請求項1乃至12のいずれか一項に記載の排ガス浄化用触媒。
- 前記アンカー・助触媒共包接粒子と、第二助触媒粒子とを含有した触媒層を耐火性無機担体にコーティングすることを特徴とする請求項1乃至13のいずれか一項に記載の排ガス浄化用触媒。
- 前記触媒層の最下層に、耐熱性無機酸化物を含有するアンダーコート層を設けることを特徴とする請求項14に記載の排ガス浄化用触媒。
- 請求項1乃至13のいずれか一項に記載の排ガス浄化用触媒の製造方法において、
前記貴金属粒子とアンカー粒子との複合粒子及び前記第一助触媒粒子を個別に又は一体的に粉砕する工程と、
粉砕された前記複合粒子及び第一助触媒粒子を、前記包接材の前駆体を含有したスラリに混合し、乾燥することにより、前記アンカー・助触媒共包接粒子を調製する工程と、
前記アンカー・助触媒共包接粒子と、前記第二助触媒粒子とを混合し、粉砕する工程と、
を有することを特徴とする排ガス浄化用触媒の製造方法。 - 内燃機関と、
前記内燃機関の排気系に装着された三元触媒と、
前記三元触媒の下流に設けられた、請求項1乃至15のいずれか一項に記載の排ガス浄化用触媒と、
を備えることを特徴とする排ガス浄化システム。
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JPWO2011062129A1 (ja) | 2013-04-04 |
EP2502672A1 (en) | 2012-09-26 |
CN102470348A (zh) | 2012-05-23 |
CN102470348B (zh) | 2013-11-06 |
US8683787B2 (en) | 2014-04-01 |
EP2502672B1 (en) | 2016-09-14 |
JP5041103B2 (ja) | 2012-10-03 |
EP2502672A4 (en) | 2015-03-25 |
US20120131911A1 (en) | 2012-05-31 |
BRPI1011498A2 (pt) | 2016-03-22 |
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