EXHAUST GAS PURIFYING CATALYST AND PRODUCTION METHOD THEREOF

Abstract

An exhaust gas purifying catalyst including: a plurality of first compounds 5 which have precious metal particles 3 supported thereon and are formed into a particle shape; and second compounds 7 which are arranged among the plurality of first compounds 5 and separate the first compounds 5 from one another, wherein pore volumes of the precious metal particles 3, the first compounds 5 and the second compounds 7 are 0.24 to 0.8 cm3/g.

Description

This application is a divisional application of U.S. application Ser. No. 12/298,461, filed Oct. 24, 2008, which is the National Stage application of International Application No. PCT/JP2007/058076, filed Apr. 12, 2007, which claims priority to Japanese Application No. 2006-126557, filed Apr. 28, 2006, and Japanese Application No. 2007-032269, filed Feb. 13, 2007. All of which are hereby incorporated by reference in their entirety.

TECHNICAL FIELD

The present invention relates to an exhaust gas purifying catalyst that purifies exhaust gas discharged from a vehicle such as an automobile, and to a production method of the exhaust gas purifying catalyst.

BACKGROUND ART

In recent years, an emission control for an automobile has been tightened up more and more, and an exhaust gas purifying catalyst has been required to purify harmful components contained in exhaust gas, for example, unburned hydrocarbon (HC) and carbon monoxide with high efficiency. The exhaust gas purifying catalyst is one in which precious metal particles are supported on a surface of a base material such as alumina. The exhaust gas purifying catalyst oxidizes the harmful components contained in the exhaust gas by the precious metal particles, and converts the harmful components into water and gas, which are harmless components. Moreover, in general, purification performance of the catalyst is enhanced as a surface area of the precious metal particles is larger, and accordingly, a particle diameter of the precious metal particles is reduced, whereby the surface area of the precious metal particles is increased, and surface energy thereof is increased.

Here, at an initial stage, the precious metal particles of the exhaust gas purifying catalyst are in a state of ultrafine particles with a diameter of several nanometers or less. However, there is a problem that, as the exhaust gas purifying catalyst is being exposed to a high-temperature oxidizing atmosphere, the surface of the precious metal particles is oxidized, the precious metal particles located in mutual vicinities are coagulated with each other and are coarsened to several ten nanometers, and the surface area of the precious metal particles is decreased, resulting in a decrease of a purification rate for such harmful substances. In order to prevent the decrease of the surface area owing to the coarsening of the precious metal particles, development regarding a production method of precious metal particles with a large surface area, such as a reversed micelle method, has been advanced.

In this reversed micelle method, first, an aqueous solution containing a surfactant and a catalyst active component (for example, a precious metal element) is mixed into an organic solvent. Thereafter, an emulsion solution, in which reversed micelles containing the aqueous solution containing the precious metal are formed, is prepared in the organic solvent, and the precious metal is deposited therein. Thereafter, the precious metal is reduced or insolubilized, and the precious metal atomized in the reversed micelle is precipitated. The reversed micelle method is a method as described above. Moreover, in Japanese Patent Laid-Open Publication No. 2000-42411, a method is disclosed, which is for producing a catalyst in such a manner that an element having an oxygen occlusion function is contained in the reversed micelles in an emulsion solution preparation step. In this reversed micelle method, the catalyst active component is supported on the base material in the reversed micelles contained in the emulsion solution, and thereafter, the reversed micelles are collapsed, and an obtained deposit is subjected to the respective steps of filtration, drying, milling and calcining, whereby the catalyst is produced. The catalyst produced by using this production method not only can support the element having the oxygen occlusion function on the base material but also supports the catalyst active component also on an outermost surface of the base material and pore surfaces formed in the base material, and accordingly, can enhance activity thereof.

However, in the above-described reversed micelle method, there has been a problem that, since the catalyst is produced by spraying and calcining the emulsion solution in which the reversed micelles are formed, a production process of the catalyst becomes complicated, leading to an increase of production cost thereof.

In this connection, it is an object of the present invention to provide an exhaust gas purifying catalyst in which a production process is simple and a high purification rate can be maintained for a long term, and to provide a production method of the exhaust gas purifying catalyst.

• Patent Document 1: Japanese Patent Laid-Open Publication No. 2000-42411

DISCLOSURE OF THE INVENTION

An exhaust gas purifying catalyst according to the present invention includes: precious metal particles which contact exhaust gas and purify harmful components; a plurality of first compounds on which the precious metal particles are supported; and second compounds which are arranged among these first compounds and separate the first compounds from one another, wherein pore volumes of these precious metal particles, first compounds and second compounds are within a range of 0.24 to 0.8 cm³/g. Moreover, a production method of an exhaust gas purifying catalyst according to the present invention includes: a supporting step of supporting precious metal particles on first compounds; a slurrying step of slurrying second compounds or a precursor of the second compounds by performing water dispersion therefor; a dispersion step of dispersing the first compounds having the precious metal particles supported thereon into the slurry of the second compounds; and a drying/calcining step of drying the slurry of the second compounds, into which the first compounds are dispersed, followed by calcining, wherein, in the dispersion step, treatment is performed under a condition where aggregates of the first compounds having the precious metal particles supported thereon are decomposed.

In accordance with the exhaust gas purifying catalyst according to the present invention and with the production method thereof, the second compounds are arranged among the plurality of first compounds having the precious metal particles supported thereon, whereby the first compounds are separated from one another by interposing the second compounds thereamong. Accordingly, even after the catalyst is used for a long term, the precious metal particles are not coagulated with each other, or the first compounds are not coagulated with each other. In such a way, a catalyst that maintains a large surface area can be obtained.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic view enlargedly showing an exhaust gas purifying catalyst according to an embodiment of the present invention.

FIG. 2 is a schematic view enlargedly showing an exhaust gas purifying catalyst according to a comparative example.

FIGS. 3A to 3C are schematic views showing a production process of the exhaust gas purifying catalyst according to the embodiment of the present invention: FIG. 3A shows a precious metal particle; FIG. 3B shows a state where the precious metal particle is supported on a first compound; and FIG. 3C shows a state where the first compounds having the precious metal particles supported thereon are covered with second compounds.

FIG. 4 is a graph for comparing temperatures at which HC(C₃H₆) purification rates of respective catalysts in Examples 1 to 10 and Comparative examples 1 and 2 become 50%.

FIG. 5 is a graph for comparing temperatures at which HC(C₃H₆) purification rates of respective catalysts in Examples 11 to 16 and Comparative examples 3 to 6 become 50%.

FIG. 6 is a graph for comparing temperatures at which HC(C₃H₆) purification rates of respective catalysts in Examples 17 to 19 and Comparative examples 7 and 8 become 50%.

FIG. 7 is a graph for comparing temperatures at which HC(C₃H₆) purification rates of respective catalysts in Examples 20 to 22 and Comparative examples 9 and 10 become 50%.

FIG. 8 is a graph for comparing temperatures at which HC(C₃H₆) purification rates of respective catalysts in Examples 23 to 25 and Comparative examples 11 and 12 become 50%.

FIG. 9 is a graph for comparing temperatures at which HC(C₃H₆) purification rates of respective catalysts in Examples 26 to 28 and Comparative example 13 become 50%.

BEST MODE FOR CARRYING OUT THE INVENTION

A description will be made below of an embodiment of the present invention based on the drawings.

[Catalyst]

FIG. 1 is a schematic view enlargedly showing a state of a cross section of an exhaust gas purifying catalyst according to the present invention.

As shown in FIG. 1, the exhaust gas purifying catalyst 1 according to the present invention includes: precious metal particles 3 as active metal that contacts exhaust gas and purifies harmful components; a plurality of first compounds 5 on which the precious metal particles 3 are supported; and second compounds 7 which are arranged among the plurality of first compounds 5 and separate the first compounds 5 from one another, wherein pore volumes of these precious metal particles 3, first compounds 5 and second compounds 7 are set within a range of 0.24 to 0.8 cm³/g. In such a way, movement and coagulation of the precious metal particles 3 can be suppressed, and in addition, mutual coagulation of the first compounds 5 can also be suppressed. Hence, a surface area of a precious metal layer composed of groups of the precious metal particles 3 can be suitably suppressed from being decreased after the catalyst 1 is exposed to the exhaust gas.

In the case of suppressing the movement of the precious metal particles 3, there is considered: (1) a chemical restraint method (anchoring method) of suppressing the movement of the precious metal particles 3 by chemically boding to the precious metal particles 3; or (2) a physical restraint method (inclusion method) of suppressing the movement of the precious metal particles 3 by covering the precious metal particles 3 with compounds. In addition to these (1) and (2), and in addition to suppression of the first compounds 5 themselves supported on the precious metal particles 3, the present invention further suppresses sintering of the precious metal particles 3.

In the case of covering the first compounds 5 having the precious metal particles 3 supported thereon with the second compounds 7, it is necessary that the exhaust gas be diffused and reach surfaces of the precious metal particles 3. For this purpose, gaps with a size of a predetermined range are required for the first compounds 5 and the second compounds 7, and these gaps just need to be formed so that the pore volumes of the precious metal particles 3, the first compounds 5 and the second compounds 7 can be set within the predetermined range. It is sufficient if an initial pore volume of the catalyst, that is, a pore volume of the catalyst before the catalyst is exposed to the exhaust gas is within a range of 0.3 to 0.8 cm³/g, and if a pore volume of the catalyst after the catalyst is exposed to the exhaust gas is within a range of 0.24 to 0.45 cm³/g. Hence, a condition to be defined is to set the pore volumes of the precious metal particles 3, the first compounds 5 and the second compounds 7 within a range of 0.24 to 0.8 cm³/g.

[Precious Metal Particle]

It is preferable that the precious metal particles 3 be composed of at least any selected from platinum (Pt), palladium (Pd) and rhodium (Rh). It is preferable that a particle diameter of the precious metal particles 3 be 1 nm to 5 nm.

[First Compound]

It is preferable that the first compounds 5 on which the precious metal particles 3 are supported be formed into a particle shape. Moreover, it is preferable that the first compounds 5 be an oxide containing Ce. Specifically, a compound containing CeO₂ and a composite oxide of Ce and Zr can be used. In the case where the first compounds 5 are the oxide containing Ce, the following combinations are preferable for the precious metal particles 3, the first compounds 5 and the second compounds 7.

• (a-1) Preferable is a combination of Pt particles as the precious metal particles 3, CeO₂ particles as the first compounds 5, and Al₂O₃ particles as the second compounds 7, that is, a combination in which the Al₂O₃ particles are arranged among the CeO₂ particles on which the Pt particles are supported.
• (a-2) Preferable is a combination of the Pt particles as the precious metal particles 3, CeZrO_x particles as the first compounds 5, and Al₂O₃ particles as the second compounds 7. Specifically, it is preferable to arrange the Al₂O₃ particles among the CeZrO_x particles on which the Pt particles are supported.
• (a-3) Preferable is a combination of the Pt particles as the precious metal particles 3, the CeO₂ particles as the first compounds 5, and ZrO₂ particles as the second compounds 7. Specifically, it is preferable to arrange the ZrO₂ particles among the CeO₂ particles on which the Pt particles are supported.
• (a-4) Preferable is a combination of the Pt particles as the precious metal particles 3, the CeO₂ particles as the first compounds 5, and a composite oxide of Al₂O₃ and ZrO₂ as the second compounds 7. Specifically, it is preferable to arrange the composite oxide of Al₂O₃ and ZrO₂ among the CeO₂ particles on which the Pt particles are supported.
• (a-5) Preferable is a combination of the Pt particles as the precious metal particles 3, the CeZrO_x particles as the first compounds 5, and the composite oxide of Al₂O₃ and ZrO₂ as the second compounds 7. Specifically, it is preferable to arrange the composite oxide of Al₂O₃ and ZrO₂ among the CeZrO_x particles on which the Pt particles are supported.

In the case where the first compounds 5 are the oxide containing CeO₂, the following combinations are preferable for the precious metal particles 3, the first compounds 5 and the second compounds 7.

• (b-1) Preferable is a combination of the Pt particles as the precious metal particles 3, the CeO₂ particles as the first compounds 5, and the Al₂O₃ particles as the second compounds 7, that is, a combination in which the Al₂O₃ particles are arranged among the CeO₂ particles on which the Pt particles are supported.
• (b-2) Preferable is a combination of the Pt particles as the precious metal particles 3, the CeO₂ particles as the first compounds 5, and the ZrO₂ particles as the second compounds 7. Specifically, it is preferable to arrange the ZrO₂ particles among the CeO₂ particles on which the Pt particles are supported.
• (b-3) Preferable is a combination of the Pt particles as the precious metal particles 3, the CeO₂ particles as the first compounds 5, and the composite oxide of Al₂O₃ and ZrO₂ as the second compounds 7. Specifically, it is preferable to arrange the composite oxide of Al₂O₃ and ZrO₂ among the CeO₂ particles on which the Pt particles are supported.

In the case where the first compounds 5 are a composite oxide containing Ce and Zr, the following combinations are preferable for the precious metal particles 3, the first compounds 5 and the second compounds 7.

• (c-1) Preferable is a combination of the Pt particles as the precious metal particles 3, the CeZrO_x particles as the first compounds 5, and the Al₂O₃ particles as the second compounds 7. Specifically, it is preferable to arrange the Al₂O₃ particles among the CeZrO_x particles on which the Pt particles are supported.
• (c-2) Preferable is a combination of the Pt particles as the precious metal particles 3, the CeZrO_x particles as the first compounds 5, and the composite oxide of Al₂O₃ and ZrO₂ as the second compounds 7. Specifically, it is preferable to arrange the composite oxide of Al₂O₃ and ZrO₂ among the CeZrO_x particles on which the Pt particles are supported.

In the case where the first compounds 5 are a composite oxide of Mn and Al, the following combinations are preferable for the precious metal particles 3, the first compounds 5 and the second compounds 7.

• (c-1) Preferable is a combination of the Pt particles as the precious metal particles 3, MnAl₂O₄ particles as the first compounds 5, and the Al₂O₃ particles as the second compounds 7. Specifically, it is preferable to arrange the Al₂O₃ particles among the MnAl₂O₄ particles on which the Pt particles are supported.

[Second Compound]

It is preferable tat the above-described second compounds 7 be an oxide containing at least any of Al and Zr. In a combination in the present invention, the best combination is a combination in which Pt—CeO₂ is covered with Al₂O₃, or in which Pt—CeZrO_x is covered with Al₂O₃. Moreover, a combination in which Pt—CeO₂ is covered with ZrO₂ is also good. Furthermore, a combination in which Pt—CeO₂ or Pt—CeZrO_x is covered with the composite oxide of Al₂O₃ and ZrO₂ is also good. Moreover, it is preferable that the above-described second compounds 7 be formed into a particle shape, and that an average particle diameter of the above-described second compounds 7 be 10 to 100 nm.

In the catalyst 1 according to the embodiment of the present invention, as shown in FIG. 1, pores 7 are formed by gaps among the particles of the second compounds 7, and by gaps among the particles of the first compounds 5 and the second compounds 7. Here, in the case where the particle diameter of the particles of the second compounds 7 is smaller than 10 nm, then, like a catalyst 11 shown in FIG. 2, the pores 9 formed of the particles of the second compounds 7 become small, and the pore volume becomes small. Therefore, the exhaust gas becomes less likely to be diffused through the pores 9, and catalyst activity of the catalyst 11 is decreased. Meanwhile, in the case where the particle diameter of the particles of the second compounds 7 becomes larger than 100 nm, then the pores formed thereof become large, and the particles of the first compounds 5 on which the precious metal particles are supported come off from the gaps among the particles of the second compounds 7, causing such an influence that the particles of the first compounds 5 are coagulated with one another.

[Production Method of Catalyst]

A production method of the catalyst according to this embodiment includes: a supporting step of supporting the precious metal particles 3 on the first compounds 5; a slurrying step of slurrying the second compounds 7 or a precursor of the second compounds 7 by performing water dispersion therefor; a dispersion step of dispersing the first compounds 5 having the precious metal particles 3 supported thereon into the slurry of the second compounds 7; and a drying/calcining step of drying the slurry of the second compounds, into which the first compounds are dispersed, followed by calcining, wherein, in the dispersion step, treatment is performed under a condition where aggregates of the first compounds 5 having the precious metal particles 3 supported thereon are decomposed.

FIGS. 3A to 3C are schematic views showing a production process of the catalyst 1 according to the embodiment of the present invention: FIG. 3A shows the precious metal particle 3; FIG. 3B shows a state where the precious metal particle 3 is supported on the first compound 5; and FIG. 3C shows the catalyst 1 in which the first compounds 5 having the precious metal particles 3 supported thereon are covered with the second compounds 7. For such treatment of decomposing the aggregates of the first compounds 5 on which the precious metal particles 3 are supported and dispersing the first compounds 5 into the second compounds 7, a method using a dispersant such as polyvinylpyrrolidone, a physical method using shear force brought by high-speed stirring, and the like can be used.

Examples

Subsequently, a description will be specifically made of the present invention through examples.

Example 1

CeO₂ particles with an average particle diameter of 30 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the CeO₂ particles, whereby CeO₂ particles having Pt supported thereon by 0.85 wt % (these are referred to as “ceria particles A”) were formed. 118.42 g of needle-like boehmite (ø10 nm×100 nm) in which moisture was contained by 24 wt % was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the ceria particles A prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder a-1 in which the ceria particles A were coated with alumina was prepared. 173.4 g of this powder a-1 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10 wt % nitric acid solution were added to the ball mill, and the powder a-1 was milled, whereby slurry with an average particle diameter of 3 μm (this is referred to as “slurry a-1”) was formed.

Next, rhodium nitrate was impregnated into a zirconium-cerium composite oxide with an average particle diameter of 20 nm, whereby particles B of the second compounds 7, which had rhodium supported thereon by 0.814%, were prepared. 118.42 g of needle-like boehmite in which moisture was contained by 24 wt % was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles B prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-1 in which the particles B were coated with alumina was prepared. 172 g of this powder b-1 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10 wt % nitric acid solution were further added to the ball mill, and the powder b-1 was milled, whereby slurry with an average particle diameter of 3 μm (this is referred to as “slurry b-1”) was formed. The slurry a-1 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of 036 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-1 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 1 was obtained. The obtained sample of Example 1 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Example 2

CeO₂ particles with an average particle diameter of 30 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the CeO₂ particles, whereby CeO₂ particles having Pt supported thereon by 0.85 wt % (these are referred to as “ceria particles A”) were formed. 113.92 g of plate-like boehmite (20×20×10 nm) in which moisture was contained by 21 wt % was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the ceria particles A prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder a-2 in which the ceria particles A were coated with alumina was prepared. 173.4 g of this powder a-2 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10 wt % nitric acid solution were added to the ball mill, and the powder a-2 was milled, whereby slurry with an average particle diameter of 3 μm (this is referred to as “slurry a-2”) was formed.

Next, rhodium nitrate was impregnated into a zirconium-cerium composite oxide with an average particle diameter of 20 nm, whereby particles B having rhodium supported thereon by 0.814% were prepared. 113.92 g of needle-like boehmite (in which moisture was contained by 21 wt %) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles B prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-2 in which the particles B were coated with alumina was prepared. 172 g of this powder b-2 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10 wt % nitric acid solution were further added to the ball mill, and the powder b-2 was milled, whereby slurry with an average particle diameter of 3 μm (this is referred to as “slurry b-2”) was formed. The slurry a-2 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of 036 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-2 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 2 was obtained. The obtained sample of Example 2 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Example 3

CeO₂ particles with an average particle diameter of 30 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the CeO₂ particles, whereby CeO₂ particles having Pt supported thereon by 0.85 wt % (these are referred to as “ceria particles A”) were formed. 105.88 g of cube-like boehmite with a dimension of 20×20×20 nm (in which moisture was contained by 15 wt %) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the ceria particles A prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder a-3 in which the ceria particles A were coated with alumina was prepared. 173.4 g of this powder a-3 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10 wt % nitric acid solution were added to the ball mill, and the powder a-3 was milled, whereby slurry with an average particle diameter of 3 μm (this is referred to as “slurry a-3”) was formed.

Next, rhodium nitrate was impregnated into a zirconium-cerium composite oxide with an average particle diameter of 20 nm, whereby particles B having rhodium supported thereon by 0.814% were prepared. 105.88 g of cube-like boehmite in which moisture was contained by 15 wt % was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles B prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-3 in which the particles B were coated with alumina was prepared. 172 g of this powder b-3 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10 wt % nitric acid solution were further added to the ball mill, and the powder b-3 was milled, whereby slurry with an average particle diameter of 3 μm (this is referred to as “slurry b-3”) was formed. The slurry a-3 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of 036 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-3 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 3 was obtained. The obtained sample of Example 3 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Example 4

CeO₂ particles with an average particle diameter of 30 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the CeO₂ particles, whereby CeO₂ particles having Pt supported thereon by 0.85 wt % (these are referred to as “ceria particles A”) were formed. 102.27 g of prism-like boehmite (20×20×60 nm) in which moisture was contained by 12 wt % was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the ceria particles A prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder a-4 in which the ceria particles A were coated with alumina was prepared. 173.4 g of this powder a-4 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10 wt % nitric acid solution were added to the ball mill, and the powder a-4 was milled, whereby slurry with an average particle diameter of 3 μm (this is referred to as “slurry a-4”) was formed.

Next, rhodium nitrate was impregnated into a zirconium-cerium composite oxide with an average particle diameter of 20 nm, whereby particles B having rhodium supported thereon by 0.814% were prepared. 102.27 g of prism-like boehmite (in which moisture was contained by 12 wt %) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles B prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-4 in which the particles B were coated with alumina was prepared. 172 g of this powder b-4 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10 wt % nitric acid solution were further added to the ball mill, and the powder b-4 was milled, whereby slurry with an average particle diameter of 3 μm (this is referred to as “slurry b-4”) was formed. The slurry a-4 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-4 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 4 was obtained. The obtained sample of Example 4 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Example 5

CeO₂ particles with an average particle diameter of 30 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the CeO₂ particles, whereby CeO₂ particles having Pt supported thereon by 0.85 wt % (these are referred to as “ceria particles A”) were formed. 90.9 g of alumina nanoparticles with an average particle diameter of 40 nm (in which moisture was contained by 1 wt %) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the ceria particles A prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder a-5 in which the ceria particles A were coated with alumina was prepared. 173.4 g of this powder a-5 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10 wt % nitric acid solution were added to the ball mill, and the powder a-5 was milled, whereby slurry with an average particle diameter of 3 μm (this is referred to as “slurry a-5”) was formed.

Next, rhodium nitrate was impregnated into a zirconium-cerium composite oxide with an average particle diameter of 20 nm, whereby particles B having rhodium supported thereon by 0.814% were prepared. 90.9 g of alumina nanoparticles with an average particle diameter of 40 nm (in which moisture was contained by 1 wt %) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles B prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-5 in which the particles B were coated with alumina was prepared. 172 g of this powder b-5 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10 wt % nitric acid solution were further added to the ball mill, and the powder b-5 was milled, whereby slurry with an average particle diameter of 3 μm (this is referred to as “slurry b-5”) was formed. The slurry a-5 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-5 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 5 was obtained. The obtained sample of Example 5 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Example 6

Cerium-zirconium composite oxide particles with an average particle diameter of 20 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the particles, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85 wt % (these are referred to as “particles C”) were formed. 118.42 g of needle-like boehmite (in which moisture was contained by 24 wt %) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles C prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder ac-6 in which the particles C were coated with alumina was prepared. 173.4 g of this powder ac-6 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10 wt % nitric acid solution were added to the ball mill, and the powder ac-6 was milled, whereby slurry with an average particle diameter of 3 μm (this is referred to as “slurry ac-6”) was formed.

Next, rhodium nitrate was impregnated into a zirconium-cerium composite oxide with an average particle diameter of 20 nm, whereby particles B having rhodium supported thereon by 0.814% were prepared. 118.42 g of needle-like boehmite (in which moisture was contained by 24 wt %) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles B prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-1 in which the particles B were coated with alumina was prepared. 172 g of this powder b-1 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10 wt % nitric acid solution were further added to the ball mill, and the powder b-1 was milled, whereby slurry with an average particle diameter of 3 μm (this is referred to as “slurry b-1”) was formed. The slurry ac-6 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-1 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 6 was obtained. The obtained sample of Example 6 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Example 7

Cerium-zirconium composite oxide particles with an average particle diameter of 20 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the particles, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85 wt % (these are referred to as “particles C”) were formed. 113.92 g of plate-like boehmite (in which moisture was contained by 21 wt %) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles C prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder ac-7 in which the particles C were coated with alumina was prepared. 173.4 g of this powder ac-7 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10 wt % nitric acid solution were added to the ball mill, and the powder ac-7 was milled, whereby slurry with an average particle diameter of 3 μm (this is referred to as “slurry ac-7”) was formed.

Next, rhodium nitrate was impregnated into a zirconium-cerium composite oxide with an average particle diameter of 20 nm, whereby particles B having rhodium supported thereon by 0.814% were prepared. 113.92 g of plate-like boehmite (in which moisture was contained by 21 wt %) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles B prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-2 in which the particles B were coated with alumina was prepared. 172 g of this powder b-2 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10 wt % nitric acid solution were further added to the ball mill, and the powder b-2 was milled, whereby slurry with an average particle diameter of 3 μm (this is referred to as “slurry b-2”) was formed. The slurry ac-7 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-2 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 7 was obtained. The obtained sample of Example 7 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Example 7

Cerium-zirconium composite oxide particles with an average particle diameter of 20 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the particles, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85 wt % (these are referred to as “particles C”) were formed. 105.88 g of cube-like boehmite (in which moisture was contained by 15 wt %) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles C prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder ac-8 in which the particles C were coated with alumina was prepared. 173.4 g of this powder ac-8 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10 wt % nitric acid solution were added to the ball mill, and the powder ac-8 was milled, whereby slurry with an average particle diameter of 3 μm (this is referred to as “slurry ac-8”) was formed.

Next, rhodium nitrate was impregnated into a zirconium-cerium composite oxide with an average particle diameter of 20 nm, whereby particles B having rhodium supported thereon by 0.814% were prepared. 105.88 g of cube-like boehmite (in which moisture was contained by 15 wt %) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles B prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-3 in which the particles B were coated with alumina was prepared. 172 g of this powder b-3 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10 wt % nitric acid solution were further added to the ball mill, and the powder b-3 was milled, whereby slurry with an average particle diameter of 3 μm (this is referred to as “slurry b-3”) was formed. The slurry ac-8 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-3 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 8 was obtained. The obtained sample of Example 8 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Example 9

Manganese aluminate particles with an average particle diameter of 40 nm were used as the first compounds 5. Dinitrodiamine Pd was impregnated into the particles, whereby manganese aluminate particles having Pd supported thereon by 0.85 wt % (these are referred to as “particles D”) were formed. 113.92 g of plate-like boehmite (in which moisture was contained by 21 wt %) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles D prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder ad-9 in which the particles D were coated with alumina was prepared. 173.4 g of this powder ad-9 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10 wt % nitric acid solution were added to the ball mill, and the powder ad-9 was milled, whereby slurry with an average particle diameter of 3 μm (this is referred to as “slurry ad-9”) was formed.

Next, rhodium nitrate was impregnated into a zirconium-cerium composite oxide with an average particle diameter of 20 nm, whereby particles B having rhodium supported thereon by 0.814% were prepared. 113.92 g of plate-like boehmite (in which moisture was contained by 21 wt %) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles B prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-2 in which the particles B were coated with alumina was prepared. 172 g of this powder b-2 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10 wt % nitric acid solution were further added to the ball mill, and the powder b-2 was milled, whereby slurry with an average particle diameter of 3 μm (this is referred to as “slurry b-2”) was formed. The slurry ad-9 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-2 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 9 was obtained. The obtained sample of Example 9 is a catalyst that individually carries thereon Pd by 0.593 g/L and Rh by 0.236 g/L.

Example 10

Manganese aluminate particles with an average particle diameter of 40 nm were used as the first compounds 5. Dinitrodiamine Pd was impregnated into the particles, whereby manganese aluminate particles having Pd supported thereon by 0.85 wt % (these are referred to as “particles D”) were formed. 105.88 g of cube-like boehmite (in which moisture was contained by 15 wt %) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles D prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder ad-10 in which the particles D were coated with alumina was prepared. 173.4 g of this powder ad-10 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10 wt % nitric acid solution were added to the ball mill, and the powder ad-10 was milled, whereby slurry with an average particle diameter of 3 μm (this is referred to as “slurry ad-10”) was formed.

Next, rhodium nitrate was impregnated into a zirconium-cerium composite oxide with an average particle diameter of 20 nm, whereby particles B having rhodium supported thereon by 0.814% were prepared. 105.88 g of cube-like boehmite (in which moisture was contained by 15 wt %) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles B prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-3 in which the particles B were coated with alumina was prepared. 172 g of this powder b-3 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10 wt % nitric acid solution were further added to the ball mill, and the powder b-3 was milled, whereby slurry with an average particle diameter of 3 μm (this is referred to as “slurry b-3”) was formed. The slurry ad-10 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of o36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-3 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 10 was obtained. The obtained sample of Example 10 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Example 11

Cerium-zirconium composite oxide particles with an average particle diameter of 30 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the particles, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles A”) were formed. 118.42 g of needle-like boehmite (100 nm×010 nm; aspect ratio: 10) (in which moisture was contained by 24%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles A prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder a-11 in which the particles A were coated with alumina was prepared (only this needle-like boehmite was calcined, and a pore volume thereof was investigated, then the pore volume was 0.8 cm³/g). 173.4 g of this powder a-11 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder a-11 was milled, whereby slurry a-11 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles with an average particle diameter of 20 nm, whereby particles B having rhodium supported thereon by 0.814 were prepared. 118.42 g of needle-like boehmite (100 nm×ø10 nm; aspect ratio: 10) (in which moisture was contained by 24%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles B prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-11 in which the particles B were coated with alumina was prepared. 172 g of this powder b-11 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 of a 10% nitric acid solution were further added to the ball mill, and the powder b-11 was milled, whereby slurry b-11 with an average particle diameter of 3 μm was formed. The slurry a-11 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-11 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 11 was obtained. The obtained sample of Example 11 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Example 12

Cerium-zirconium composite oxide particles with an average particle diameter of 30 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the ceria-zirconium particles, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles A”) were formed. 113.92 g of plate-like boehmite (10×20×20 nm; aspect ratio: 0.5) (in which moisture was contained by 21%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles A prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder a-12 in which the particles A were coated with alumina was prepared (only this plate-like boehmite was calcined, and a pore volume thereof was investigated, then the pore volume was 0.85 cm³/g). 173.4 g of this powder a-12 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder a-12 was milled, whereby slurry a-12 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles with an average particle diameter of 20 nm, whereby particles B having rhodium supported thereon by 0.814% were prepared. 113.92 g of plate-like boehmite (10×20×20 nm; aspect ratio: 0.5) (in which moisture was contained by 21%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles B prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-12 in which the particles B were coated with alumina was prepared. 172 g of this powder b-12 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder b-12 was milled, whereby slurry b-12 with an average particle diameter of 3 μm was formed. The slurry a-12 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-12 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 12 was obtained. The obtained sample of Example 12 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Example 13

Cerium-zirconium composite oxide particles with an average particle diameter of 30 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the cerium-zirconium composite oxide particles, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles A”) were formed. 105.88 g of cube-like boehmite (20×20×20 nm; aspect ratio: 1) (in which moisture was contained by 15%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles A prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder a-13 in which the particles A were coated with alumina was prepared (only this cube-like boehmite was calcined, and a pore volume thereof was investigated, then the pore volume was 0.9 cm³/g). 173.4 g of this powder a-13 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder a-13 was milled, whereby slurry a-13 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles with an average particle diameter of 20 nm, whereby particles B having rhodium supported thereon by 0.814% were prepared. 105.88 g of cube-like boehmite (20×20×20 nm; aspect ratio: 1) (in which moisture was contained by 15%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles B prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-13 in which the particles B were coated with alumina was prepared. 172 g of this powder b-13 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder b-13 was milled, whereby slurry b-13 with an average particle diameter of 3 μm was formed. The slurry a-13 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-13 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 13 was obtained. The obtained sample of Example 13 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Example 14

Cerium-zirconium composite oxide particles with an average particle diameter of 30 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the cerium-zirconium composite oxide particles, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles A”) were formed. 102.27 g of prism-like boehmite (60×20×20 nm; aspect ratio: 3) (in which moisture was contained by 12%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles A prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder a-14 in which the particles A were coated with alumina was prepared (only this prism-like boehmite was calcined, and a pore volume thereof was investigated, then the pore volume was 1.0 cm³/g). 173.4 g of this powder a-14 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder a-14 was milled, whereby slurry a-14 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles with an average particle diameter of 20 nm, whereby particles B having rhodium supported thereon by 0.814% were prepared. 102.27 g of prism-like boehmite (60×20×20 nm; aspect ratio: 3) (in which moisture was contained by 12%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles B prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-14 in which the particles B were coated with alumina was prepared. 172 g of this powder b-14 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder b-14 was milled, whereby slurry b-14 with an average particle diameter of 3 μm was formed. The slurry a-14 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-14 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 14 was obtained. The obtained sample of Example 14 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Example 15

Cerium-zirconium composite oxide particles with an average particle diameter of 20 nm were used as the first compounds 5. Dinitrodiamine Pd was impregnated into the cerium-zirconium composite oxide particles, whereby cerium-zirconium composite oxide particles having Pd supported thereon by 0.85% (these are referred to as “particles C”) were formed. 113.92 g of plate-like boehmite (10×20×20 nm; aspect ratio: 0.5) (in which moisture was contained by 21%) was put into a beaker, dispersed into water, and made acidic. To a resultant thus obtained, 90 g of the particles C prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder ad-15 in which the particles C were coated with alumina was prepared. 173.4 g of this powder ad-15 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder ad-15 was milled, whereby slurry ad-15 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles with an average particle diameter of 20 nm, whereby particles B having rhodium supported thereon by 0.814% were prepared. 113.92 g of plate-like boehmite (10×20×20 nm; aspect ratio: 0.5) (in which moisture was contained by 21%) was put into a beaker, dispersed into water, and made acidic. To a resultant thus obtained, 90 g of the particles B prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-12 in which the particles B were coated with alumina was prepared. 172 g of this powder b-12 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder b-12 was milled, whereby slurry b-12 with an average particle diameter of 3 μm was formed. The slurry ad-15 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-12 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 15 was obtained. The obtained sample of Example 15 is a catalyst that individually carries thereon Pd by 0.593 g/L and Rh by 0.236 g/L.

Example 16

Cerium-zirconium composite oxide particles with an average particle diameter of 20 nm were used as the first compounds 5. Dinitrodiamine Pd was impregnated into the particles, whereby cerium-zirconium composite oxide particles having Pd supported thereon by 0.85% (these are referred to as “particles C”) were formed. 105.88 g of cube-like boehmite (20×20×20 nm; aspect ratio: 1) (in which moisture was contained by 15%) was put into a beaker, dispersed into water, and made acidic. To a resultant thus obtained, 90 g of the particles C prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder ad-16 in which the particles C were coated with alumina was prepared. 173.4 g of this powder ad-16 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder ad-16 was milled, whereby slurry ad-16 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles with an average particle diameter of 20 nm, whereby particles B having rhodium supported thereon by 0.814% were prepared. 105.88 g of cube-like boehmite (20×20×20 nm; aspect ratio: 1) (in which moisture was contained by 15%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles B prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-13 in which the particles B were coated with alumina was prepared. 172 g of this powder b-13 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder b-13 was milled, whereby slurry b-13 with an average particle diameter of 3 μm was formed. The slurry ad-16 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-13 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 16 was obtained. The obtained sample of Example 16 is a catalyst that individually carries thereon Pd by 0.593 g/L and Rh by 0.236 g/L.

Example 17

Cerium-zirconium composite oxide particles with a pore volume of 0.18 cm³/g were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the particles, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles D1”) were formed. 105.88 g of cube-like boehmite (20×20×20 nm) (in which moisture was contained by 15%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles D1 prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder a-17 in which the particles D1 were coated with alumina was prepared. 173.4 g of this powder a-17 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder a-17 was milled, whereby slurry a-17 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles with a pore volume of 0.28 cm³/g, whereby particles El having rhodium supported thereon by 0.814% were prepared. 105.88 g of cube-like boehmite (20×20×20 nm) (in which moisture was contained by 15%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles E1 prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-17 in which the particles E1 were coated with alumina was prepared. 172 g of this powder b-17 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder b-17 was milled, whereby slurry b-17 with an average particle diameter of 3 μm was formed. The slurry a-17 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-17 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 17 was obtained. The obtained sample of Example 17 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Example 18

Cerium-zirconium composite oxide particles with a pore volume of 0.28 cm³/g were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the particles, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles D2”) were formed. 105.88 g of cube-like boehmite (20×20×20 nm) (in which moisture was contained by 15%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles D2 prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder a-18 in which the particles D2 were coated with alumina was prepared. 173.4 g of this powder a-18 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder a-18 was milled, whereby slurry a-18 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles with a pore volume of 0.30 cm³/g, whereby particles E2 having rhodium supported thereon by 0.814% were prepared. 105.88 g of cube-like boehmite (20×20×20 nm) (in which moisture was contained by 15%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles E2 prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-18 in which the particles E2 were coated with alumina was prepared. 172 g of this powder b-18 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder b-18 was milled, whereby slurry b-18 with an average particle diameter of 3 μm was formed. The slurry a-18 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-18 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 18 was obtained. The obtained sample of Example 18 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Example 19

Cerium-zirconium composite oxide particles with a pore volume of 0.30 cm³/g were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the particles, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles D3”) were formed. 105.88 g of cube-like boehmite (20×20×20 nm) (in which moisture was contained by 15%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles D3 prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder a-19 in which the particles D3 were coated with alumina was prepared. 173.4 g of this powder a-19 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder a-19 was milled, whereby slurry a-19 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles with a pore volume of 0.32 cm³/g, whereby particles E3 having rhodium supported thereon by 0.814% were prepared. 105.88 g of cube-like boehmite (20×20×20 nm) (in which moisture was contained by 15%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles E3 prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-19 in which the particles E3 were coated with alumina was prepared. 172 g of this powder b-19 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder b-19 was milled, whereby slurry b-19 with an average particle diameter of 3 μm was formed. The slurry a-19 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-19 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 19 was obtained. The obtained sample of Example 19 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Example 20

Cerium-zirconium composite oxide particles in which cerium occupied 74% and zirconium occupied 26% in terms of composition were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the particles, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles F1”) were formed. 105.88 g of cube-like boehmite (20×20×20 nm) (in which moisture was contained by 15%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles F1 prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder a-20 in which the particles F1 were coated with alumina was prepared. 173.4 g of this powder a-20 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder a-20 was milled, whereby slurry a-20 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles in which zirconium occupied 95% and lanthanum occupied 5% in terms of composition, whereby particles G1 having rhodium supported thereon by 0.814% were prepared. 105.88 g of cube-like boehmite (20×20×20 nm) (in which moisture was contained by 15%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles G1 prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-20 in which the particles G1 were coated with alumina was prepared. 172 g of this powder b-20 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder b-20 was milled, whereby slurry b-20 with an average particle diameter of 3 μm was formed. The slurry a-20 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-20 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 20 was obtained. The obtained sample of Example 20 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Example 21

Cerium-zirconium composite oxide particles in which cerium occupied 78% and zirconium occupied 22% in terms of composition were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the particles, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles F2”) were formed. 105.88 g of cube-like boehmite (20×20×20 nm) (in which moisture was contained by 15%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles F2 prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder a-21 in which the particles F2 were coated with alumina was prepared. 173.4 g of this powder a-21 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder a-21 was milled, whereby slurry a-21 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles in which zirconium occupied 97% and lanthanum occupied 3% in terms of composition, whereby particles G2 having rhodium supported thereon by 0.814% were prepared. 105.88 g of cube-like boehmite (20×20×20 nm) (in which moisture was contained by 15%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles G2 prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-21 in which the particles G2 were coated with alumina was prepared. 172 g of this powder b-21 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder b-21 was milled, whereby slurry b-21 with an average particle diameter of 3 μm was formed. The slurry a-21 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-21 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 21 was obtained. The obtained sample of Example 21 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Example 22

Cerium-zirconium composite oxide particles in which cerium occupied 80% and zirconium occupied 20% in terms of composition were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the particles, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles F3”) were formed. 105.88 g of cube-like boehmite (20×20×20 nm) (in which moisture was contained by 15%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles F3 prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder a-22 in which the particles F3 were coated with alumina was prepared. 173.4 g of this powder a-22 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder a-22 was milled, whereby slurry a-22 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles in which zirconium occupied 99% and lanthanum occupied 1% in terms of composition, whereby particles G3 having rhodium supported thereon by 0.814% were prepared. 105.88 g of cube-like boehmite (20×20×20 nm) (in which moisture was contained by 15%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles G3 prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-22 in which the particles G3 were coated with alumina was prepared. 172 g of this powder b-22 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder b-22 was milled, whereby slurry b-22 with an average particle diameter of 3 μm was formed. The slurry a-22 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-22 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 22 was obtained. The obtained sample of Example 22 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Example 23

Cerium-zirconium composite oxide particles with an average particle diameter of 30 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the particles, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles A”) were formed. 105.04 g of needle-like boehmite (ø10 nm×100 nm) (in which moisture was contained by 24.6%) was put into a beaker into which water was poured, cerium nitrate was added thereto so that an amount thereof as cerium oxide could be 4.5 g, and zirconyl nitrate was dispersed into the water so that an amount thereof as zirconium oxide could be 6.3 g. To a resultant thus obtained, 90 g of the particles A prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder a-23 in which the particles A were coated with alumina was prepared. 173.4 g of this powder a-23 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder a-23 was milled, whereby slurry a-23 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles with an average particle diameter of 20 nm, whereby particles B having rhodium supported thereon by 0.814% were prepared. 118.42 g of needle-like boehmite (in which moisture was contained by 24%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles B prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-11 in which the particles B were coated with alumina was prepared. 172 g of this powder b-11 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder b-11 was milled, whereby slurry b-11 with an average particle diameter of 3 μm was formed. The slurry a-23 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-11 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 23 was obtained. The obtained sample of Example 23 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Example 24

Cerium-zirconium composite oxide particles with an average particle diameter of 30 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the particles, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles A”) were formed. 101.46 g of needle-like boehmite (ø10 nm×100 nm) (in which moisture was contained by 24.6%) was put into a beaker into which water was poured, cerium nitrate was added thereto so that an amount thereof as cerium oxide could be 9 g, and zirconyl nitrate was dispersed into the water so that an amount thereof as zirconium oxide could be 4.5 g. To a resultant thus obtained, 90 g of the particles A prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder a-24 in which the particles A were coated with alumina was prepared. 173.4 g of this powder a-24 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder a-24 was milled, whereby slurry a-24 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles with an average particle diameter of 20 nm, whereby particles B having rhodium supported thereon by 0.814% were prepared. 118.42 g of needle-like boehmite (in which moisture was contained by 24%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles B prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-11 in which the particles B were coated with alumina was prepared. 172 g of this powder b-11 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder b-11 was milled, whereby slurry b-11 with an average particle diameter of 3 μm was formed. The slurry a-24 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-11 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 24 was obtained. The obtained sample of Example 24 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Example 25

Cerium-zirconium composite oxide particles with an average particle diameter of 30 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the particles, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles A”) were formed. 97.88 g of needle-like boehmite (ø10 nm×100 nm) (in which moisture was contained by 24.6%) was put into a beaker into which water was poured, cerium nitrate was added thereto so that an amount thereof as cerium oxide could be 13.5 g, and zirconyl nitrate was dispersed into the water so that an amount thereof as zirconium oxide could be 2.7 g. To a resultant thus obtained, 90 g of the particles A prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder a-25 in which the particles A were coated with alumina was prepared. 173.4 g of this powder a-25 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder a-25 was milled, whereby slurry a-25 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles with an average particle diameter of 20 nm, whereby particles B having rhodium supported thereon by 0.814% were prepared. 118.42 g of needle-like boehmite (in which moisture was contained by 24%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles B prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-11 in which the particles B were coated with alumina was prepared. 172 g of this powder b-11 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder b-11 was milled, whereby slurry b-11 with an average particle diameter of 3 μm was formed. The slurry a-25 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-11 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 25 was obtained. The obtained sample of Example 25 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Example 26

Cerium-zirconium composite oxide particles with an average particle diameter of 30 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the cerium-zirconium composite oxide particles, and a resultant was calcined at 700° C. for two hours, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles I1”) were formed. A degree of dispersion of Pt in the particles I1 was 50%. 105.88 g of cube-like boehmite (20×20×20 nm) (in which moisture was contained by 15%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles I1 prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder a-26 in which the particles I1 were coated with alumina was prepared. A degree of dispersion of Pt in the particles was 35%. 173.4 g of this powder a-26 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder a-26 was milled, whereby slurry a-26 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles with an average particle diameter of 20 nm, and a resultant was calcined at 400° C. for one hour, whereby zirconium-lanthanum composite oxide particles having rhodium supported thereon by 0.814% (these are referred to as “particles J1”) were prepared. A degree of dispersion of Rh in the particles J1 was 56%. 105.88 g of cube-like boehmite (in which moisture was contained by 15%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles J1 prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-26 in which the particles J1 were coated with alumina was prepared. A degree of dispersion of Rh in the powder was 38%. 172 g of this powder b-26 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder b-26 was milled, whereby slurry b-26 with an average particle diameter of 3 μm was formed. The slurry a-26 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-26 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 26 was obtained. The obtained sample of Example 26 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Example 27

Cerium-zirconium composite oxide particles with an average particle diameter of 30 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the cerium-zirconium composite oxide particles, and a resultant was calcined at 600° C. for two hours, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles I2”) were formed. A degree of dispersion of Pt in the particles I2 was 50%. 105.88 g of cube-like boehmite (20×20×20 nm) (in which moisture was contained by 15%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles 12 prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder a-27 in which the particles 12 were coated with alumina was prepared. A degree of dispersion of Pt in the particles a-27 was 50%. 173.4 g of this powder a-27 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder a-27 was milled, whereby slurry a-27 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles with an average particle diameter of 20 nm, and a resultant was calcined at 400° C. for one hour, whereby the particles J1 having rhodium supported thereon by 0.814% were prepared. A degree of dispersion of Rh in the particles J1 was 56%. 105.88 g of cube-like boehmite (in which moisture was contained by 15%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles J1 prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-27 in which the particles J1 were coated with alumina was prepared. A degree of dispersion of Rh in the powder b-27 was 38%. 172 g of this powder b-27 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder b-27 was milled, whereby slurry b-27 with an average particle diameter of 3 μm was formed. The slurry a-27 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-27 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 27 was obtained. The obtained sample of Example 27 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Example 28

Cerium-zirconium composite oxide particles with an average particle diameter of 30 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the cerium-zirconium composite oxide particles, and a resultant was calcined at 400° C. for one hour, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles I3”) were formed. A degree of dispersion of Pt in the particles I3 was 100%. 105.88 g of cube-like boehmite (20×20×20 nm) (in which moisture was contained by 15%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles I3 prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder a-28 in which the particles I3 were coated with alumina was prepared. A degree of dispersion of Pt in the powder was 80%. 173.4 g of this powder a-28 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder a-28 was milled, whereby slurry a-28 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles with an average particle diameter of 20 nm, and a resultant was calcined at 400° C. for one hour, whereby the particles J1 having rhodium supported thereon by 0.814% were prepared. A degree of dispersion of Rh in the particles J1 was 56%. 105.88 g of cube-like boehmite (in which moisture was contained by 15%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles J1 prepared in advance was added, and was dispersed thereinto by the high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder b-28 in which the particles J1 were coated with alumina was prepared. A degree of dispersion of Rh in the powder b-28 was 38%. 172 g of this powder b-28 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder b-28 was milled, whereby slurry b-28 with an average particle diameter of 3 μm was formed. The slurry a-28 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry b-28 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Example 28 was obtained. The obtained sample of Example 28 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Comparative Example 1

CeO₂ particles with an average particle diameter of 30 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the CeO₂ particles, whereby CeO₂ particles having Pt supported thereon by 0.85% (these are referred to as “ceria particles A”) were formed. Aluminum isopropoxide equivalent to 90 g of Al₂O₃ was dissolved into 2-methyl-2,4-pentanediol. To a solution thus obtained, 90 g of the ceria particles A was added, and water was further added thereto, whereby hydrolysis was performed therefor. The water and organic matter such as the 2-methyl-2,4-pentanediol were evaporated and dried, followed by calcining, whereby powder c-1 in which the particles A were coated with alumina was prepared. An average particle diameter of the alumina was 7 to 8 nm. 173.4 g of this powder c-1 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10 wt % nitric acid solution were added to the ball mill, and the powder c-1 was milled, whereby slurry with an average particle diameter of 3 μm (this is referred to as “slurry c-1”) was formed.

Next, rhodium nitrate was impregnated into zirconium-cerium composite oxide particles with an average particle diameter of 20 nm, whereby particles B having rhodium supported thereon by 0.814% were prepared. 562.5 g of zirconia sol with an average particle diameter of 8 nm (in which moisture was contained by 84%) was put into a beaker, and 90 g of the particles B prepared in advance was added thereto, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder cb-1 in which the particles B were coated with alumina was prepared. 172 g of this powder cb-1 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10 wt % nitric acid solution were further added to the ball mill, and the powder cb-1 was milled, whereby slurry with an average particle diameter of 3 μm (this is referred to as “slurry cb-1”) was formed. The slurry c-1 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry cb-1 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Comparative example 1 was obtained. The obtained sample of Comparative example 1 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Comparative example 2

CeO₂ particles with an average particle diameter of 30 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the CeO₂ particles, whereby CeO₂ particles having Pt supported thereon by 0.85% (these are referred to as “ceria particles A”) were formed. 90.9 g of alumina nanoparticles with an average particle diameter of 110 nm (in which moisture was contained by 1 wt %) was put into a beaker, dispersed into water, and made acidic. To a resultant thus obtained, 90 g of the ceria particles A prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder c-2 in which the ceria particles A were coated with alumina was prepared. 173.4 g of this powder c-2 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10 wt % nitric acid solution were added to the ball mill, and the powder c-2 was milled, whereby slurry with an average particle diameter of 3 μm (this is referred to as “slurry c-2”) was formed.

Next, rhodium nitrate was impregnated into zirconium-cerium composite oxide particles with an average particle diameter of 20 nm, whereby particles B having rhodium supported thereon by 0.814% were prepared. 90.9 g of alumina nanoparticles with an average particle diameter of 110 nm (in which moisture was contained by 1%) was put into a beaker, dispersed into water, and made acidic. To a resultant thus obtained, 90 g of the particles B prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder cb-2 in which the particles B were coated with alumina was prepared. 172 g of this powder cb-2 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10 wt % nitric acid solution were further added to the ball mill, and the powder cb-2 was milled, whereby slurry with an average particle diameter of 3 μm (this is referred to as “slurry cb-2”) was formed. The slurry c-2 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry cb-2 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Comparative example 2 was obtained. The obtained sample of Comparative example 2 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Comparative Example 3

Cerium-zirconium composite oxide particles with an average particle diameter of 30 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the cerium-zirconium composite oxide particles, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles A”) were formed. Aluminum isopropoxide equivalent to 90 g of Al₂O₃ was dissolved into 2-methyl-2,4-pentanediol. To a solution thus obtained, 90 g of the particles A was added, and water was further added thereto, whereby hydrolysis was performed therefor. The water and organic matter such as the 2-methyl-2,4-pentanediol were evaporated and dried, followed by calcining, whereby powder c-3 in which the particles A were coated with alumina was prepared. An average particle diameter of the alumina was 7 to 8 nm. 173.4 g of this powder c-3 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder c-3 was milled, whereby slurry c-3 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles with an average particle diameter of 20 nm, whereby particles B having rhodium supported thereon by 0.814% were prepared. Aluminum isopropoxide equivalent to 90 g of Al₂O₃ was dissolved into 2-methyl-2,4-pentanediol. To a solution thus obtained, 90 g of the particles B was added, and water was further added thereto, whereby hydrolysis was performed therefor. The water and organic matter such as the 2-methyl-2,4-pentanediol were evaporated and dried, followed by calcining, whereby powder cb-3 in which the particles B were coated with alumina was prepared. 172 g of this powder cb-3 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder cb-3 was milled, whereby slurry cb-3 with an average particle diameter of 3 μm was formed. The slurry c-3 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry cb-3 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Comparative example 3 was obtained. The obtained sample of Comparative example 3 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Comparative Example 4

Cerium-zirconium composite oxide particles with an average particle diameter of 30 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the cerium-zirconium composite oxide particles, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles A”) were formed. 90.9 g of alumina nanoparticles with an average particle diameter of 130 nm (in which moisture was contained by 1 wt %) was put into a beaker, dispersed into water, and made acidic. To a resultant thus obtained, 90 g of the particles A prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder c-4 in which the particles A were coated with alumina was prepared. 173.4 g of this powder c-4 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10 wt % nitric acid solution were added to the ball mill, and the powder c-4 was milled, whereby slurry c-4 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles with an average particle diameter of 20 nm, whereby particles B having rhodium supported thereon by 0.814% were prepared. 90.9 g of alumina nanoparticles with an average particle diameter of 130 nm (in which moisture was contained by 1%) was put into a beaker, dispersed into water, and made acidic. To a resultant thus obtained, 90 g of the particles B prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder cb-4 in which the particles B were coated with alumina was prepared. 172 g of this powder cb-4 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder cb-4 was milled, whereby slurry cb-4 with an average particle diameter of 3 μm was formed. The slurry c-4 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry cb-4 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Comparative example 4 was obtained. The obtained sample of Comparative example 4 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Comparative Example 5

Cerium-zirconium composite oxide particles with an average particle diameter of 30 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the particles, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles A”) were formed. 120 g of needle-like boehmite (150 nm×010 nm; aspect ratio: 15) (in which moisture was contained by 25%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles A prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder c-5 in which the particles A were coated with alumina was prepared (only this needle-like boehmite was calcined, and a pore volume thereof was investigated, then the pore volume was 0.7 cm³/g). 173.4 g of this powder c-5 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder c-5 was milled, whereby slurry c-5 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles with an average particle diameter of 20 nm, whereby particles B having rhodium supported thereon by 0.814% were prepared. 120 g of needle-like boehmite (150 nm×ø10 nm; aspect ratio: 15) (in which moisture was contained by 25%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles B prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder cb-5 in which the particles B were coated with alumina was prepared. 172 g of this powder cb-5 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder cb-5 was milled, whereby slurry cb-5 with an average particle diameter of 3 μm was formed. The slurry c-5 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry cb-5 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Comparative example 5 was obtained. The obtained sample of Comparative example 5 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Comparative Example 6

Cerium-zirconium composite oxide particles with an average particle diameter of 30 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the cerium-zirconium particles, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles A”) were formed. 113.92 g of plate-like boehmite (5×20×20 nm; aspect ratio: 0.25) (in which moisture was contained by 21%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles A prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder c-6 in which the particles A were coated with alumina was prepared (only this plate-like boehmite was calcined, and a pore volume thereof was investigated, then the pore volume was 0.85 cm³/g). 173.4 g of this powder c-6 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder c-6 was milled, whereby slurry c-6 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles with an average particle diameter of 20 nm, whereby particles B having rhodium supported thereon by 0.814% were prepared. 113.92 g of plate-like boehmite (5×20×20 nm; aspect ratio: 0.25) (in which moisture was contained by 21%) was put into a beaker, dispersed into water, and deflocculated by acid. To a resultant thus obtained, 90 g of the particles B prepared in advance was added, and was dispersed thereinto by high-speed stirring. Thereafter, slurry thus obtained was dried and calcined, whereby powder cb-6 in which the particles B were coated with alumina was prepared. 172 g of this powder cb-6 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder cb-6 was milled, whereby slurry cb-6 with an average particle diameter of 3 μm was formed. The slurry c-6 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry cb-6 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Comparative example 6 was obtained. The obtained sample of Comparative example 6 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Comparative Example 7

Cerium-zirconium composite oxide particles with a pore volume of 0.15 cm³/g were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the particles, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles D4”) were formed. Aluminum isopropoxide equivalent to 90 g of Al₂O₃ was dissolved into 2-methyl-2,4-pentanediol. To a solution thus obtained, 90 g of the particles D4 was added, and water was further added thereto, whereby hydrolysis was performed therefor. The water and organic matter such as the 2-methyl-2,4-pentanediol were evaporated and dried, followed by calcining, whereby powder c-7 in which the particles D4 were coated with alumina was prepared. 173.4 g of this powder c-7 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10 wt % nitric acid solution were added to the ball mill, and the powder c-7 was milled, whereby slurry c-7 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles with a pore volume of 0.16 cm³/g, whereby particles E4 having rhodium supported thereon by 0.814% were prepared. Aluminum isopropoxide equivalent to 90 g of Al₂O₃ was dissolved into 2-methyl-2,4-pentanediol. To a solution thus obtained, 90 g of the particles E4 was added, and water was further added thereto, whereby hydrolysis was performed therefor. The water and organic matter such as the 2-methyl-2,4-pentanediol were evaporated and dried, followed by calcining, whereby powder cb-7 in which the particles E4 were coated with alumina was prepared. 172 g of this powder cb-7 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder cb-7 was milled, whereby slurry cb-7 with an average particle diameter of 3 μm was formed. The slurry c-7 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry cb-7 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Comparative example 7 was obtained. The obtained sample of Comparative example 7 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Comparative Example 8

Cerium-zirconium composite oxide particles with a pore volume of 0.4 cm³/g were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the particles, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles D5”) were formed. Aluminum isopropoxide equivalent to 90 g of Al₂O₃ was dissolved into 2-methyl-2,4-pentanediol. To a solution thus obtained, 90 g of the particles D5 was added, and water was further added thereto, whereby hydrolysis was performed therefor. The water and organic matter such as the 2-methyl-2,4-pentanediol were evaporated and dried, followed by calcining, whereby powder c-8 in which the particles D5 were coated with alumina was prepared. 173.4 g of this powder c-8 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder c-8 was milled, whereby slurry c-8 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles with a pore volume of 0.41 cm³/g, whereby particles E5 having rhodium supported thereon by 0.814% were prepared. Aluminum isopropoxide equivalent to 90 g of Al₂O₃ was dissolved into 2-methyl-2,4-pentanediol. To a solution thus obtained, 90 g of the particles E5 was added, and water was further added thereto, whereby hydrolysis was performed therefor. The water and organic matter such as the 2-methyl-2,4-pentanediol were evaporated and dried, followed by calcining, whereby powder cb-8 in which the particles E5 were coated with alumina was prepared. 172 g of this powder cb-8 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder cb-8 was milled, whereby slurry cb-8 with an average particle diameter of 3 μm was formed. The slurry c-8 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry cb-8 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Comparative example 8 was obtained. The obtained sample of Comparative example 8 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Comparative Example 9

Cerium-zirconium composite oxide particles in which cerium oxide occupied 70% and zirconium oxide occupied 30% in terms of composition were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the particles, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles F4”) were formed. Aluminum isopropoxide equivalent to 90 g of Al₂O₃ was dissolved into 2-methyl-2,4-pentanediol. To a solution thus obtained, 90 g of the particles F4 was added, and water was further added thereto, whereby hydrolysis was performed therefor. The water and organic matter such as the 2-methyl-2,4-pentanediol were evaporated and dried, followed by calcining, whereby powder c-9 in which the particles F4 were coated with alumina was prepared. 173.4 g of this powder c-9 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder c-9 was milled, whereby slurry c-9 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles in which zirconium occupied 90% and lanthanum occupied 10%, whereby particles G4 having rhodium supported thereon by 0.814% were prepared. Aluminum isopropoxide equivalent to 90 g of Al₂O₃ was dissolved into 2-methyl-2,4-pentanediol. To a solution thus obtained, 90 g of the particles G4 was added, and water was further added thereto, whereby hydrolysis was performed therefor. The water and organic matter such as the 2-methyl-2,4-pentanediol were evaporated and dried, followed by calcining, whereby powder cb-9 in which the particles G4 were coated with alumina was prepared. 172 g of this powder cb-9 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder cb-9 was milled, whereby slurry cb-9 with an average particle diameter of 3 μm was formed. The slurry c-9 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry cb-9 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Comparative example 9 was obtained. The obtained sample of Comparative example 9 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Comparative Example 10

Cerium-zirconium composite oxide particles in which cerium oxide occupied 90% and zirconium oxide occupied 10% in terms of composition were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the particles, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles F5”) were formed. Aluminum isopropoxide equivalent to 90 g of Al₂O₃ was dissolved into 2-methyl-2,4-pentanediol. To a solution thus obtained, 90 g of the particles F5 was added, and water was further added thereto, whereby hydrolysis was performed therefor. The water and organic matter such as the 2-methyl-2,4-pentanediol were evaporated and dried, followed by calcining, whereby powder c-10 in which the particles F5 were coated with alumina was prepared. 173.4 g of this powder c-10 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder c-10 was milled, whereby slurry c-10 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconia particles in which zirconia occupied 100%, whereby particles G5 having rhodium supported thereon by 0.814% were prepared. Aluminum isopropoxide equivalent to 90 g of Al₂O₃ was dissolved into 2-methyl-2,4-pentanediol. To a solution thus obtained, 90 g of the particles G5 was added, and water was further added thereto, whereby hydrolysis was performed therefor. The water and organic matter such as the 2-methyl-2,4-pentanediol were evaporated and dried, followed by calcining, whereby powder cb-10 in which the particles G5 were coated with alumina was prepared. 172 g of this powder cb-10 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder cb-10 was milled, whereby slurry cb-10 with an average particle diameter of 3 μm was formed. The slurry c-10 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry cb-10 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Comparative example 10 was obtained. The obtained sample of Comparative example 10 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Comparative Example 11

Cerium-zirconium composite oxide particles with an average particle diameter of 30 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the particles, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles A”) were formed. Aluminum isopropoxide equivalent to 87.3 g of Al₂O₃ was dissolved into 2-methyl-2,4-pentanediol. To a solution thus obtained, cerium acetylacetonate was added so that an amount thereof as cerium oxide could be 1.8 g, and moreover, zirconium acetylacetonate was added so that an amount thereof as zirconium oxide could be 0.9 g. To a resultant thus obtained, 90 g of the particles A was added, and water was further added thereto, whereby hydrolysis was performed therefor. The water and organic matter such as the 2-methyl-2,4-pentanediol were evaporated and dried, followed by calcining, whereby powder c-11 in which the particles A were coated with alumina was prepared. 173.4 g of this powder c-11 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder c-11 was milled, whereby slurry c-11 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles with an average particle diameter of 20 nm, whereby particles B having rhodium supported thereon by 0.814% were prepared. Aluminum isopropoxide equivalent to 90 g of Al₂O₃ was dissolved into 2-methyl-2,4-pentanediol. To a solution thus obtained, 90 g of the particles B was added, and water was further added thereto, whereby hydrolysis was performed therefor. The water and organic matter such as the 2-methyl-2,4-pentanediol were evaporated and dried, followed by calcining, whereby powder cb-3 in which the particles B were coated with alumina was prepared. 172 g of this powder cb-3 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder cb-3 was milled, whereby slurry cb-3 with an average particle diameter of 3 μm was formed. The slurry c-11 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry cb-3 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Comparative example 11 was obtained. The obtained sample of Comparative example 11 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Comparative Example 12

Cerium-zirconium composite oxide particles with an average particle diameter of 30 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the particles, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles A”) were formed. Aluminum isopropoxide equivalent to 63 g of Al₂O₃ was dissolved into 2-methyl-2,4-pentanediol. To a solution thus obtained, cerium acetylacetonate was added so that an amount thereof as cerium oxide could be 18.0 g, and moreover, zirconium acetylacetonate was added so that an amount thereof as zirconium oxide could be 9.0 g. To a resultant thus obtained, 90 g of the particles A was added, and water was further added thereto, whereby hydrolysis was performed therefor. The water and organic matter such as the 2-methyl-2,4-pentanediol were evaporated and dried, followed by calcining, whereby powder c-12 in which the particles A were coated with alumina was prepared. 173.4 g of this powder c-12 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder c-12 was milled, whereby slurry c-12 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles with an average particle diameter of 20 nm, whereby particles B having rhodium supported thereon by 0.814% were prepared. Aluminum isopropoxide equivalent to 90 g of Al₂O₃ was dissolved into 2-methyl-2,4-pentanediol. To a solution thus obtained, 90 g of the particles B was added, and water was further added thereto, whereby hydrolysis was performed therefor. The water and organic matter such as the 2-methyl-2,4-pentanediol were evaporated and dried, followed by calcining, whereby powder cb-3 in which the particles B were coated with alumina was prepared. 172 g of this powder cb-3 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder cb-3 was milled, whereby slurry cb-3 with an average particle diameter of 3 μm was formed. The slurry c-12 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry cb-3 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Comparative example 12 was obtained. The obtained sample of Comparative example 12 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

Comparative Example 13

Cerium-zirconium composite oxide particles with an average particle diameter of 30 nm were used as the first compounds 5. Dinitrodiamine Pt was impregnated into the particles, and a resultant was calcined at 800° C. for two hours, whereby cerium-zirconium composite oxide particles having Pt supported thereon by 0.85% (these are referred to as “particles I4”) were formed. A degree of dispersion of Pt in the particles I4 was 40%. Aluminum isopropoxide equivalent to 90 g of Al₂O₃ was dissolved into 2-methyl-2,4-pentanediol. To a solution thus obtained, 90 g of the particles I4 was added, and water was further added thereto, whereby hydrolysis was performed therefor. The water and organic matter such as the 2-methyl-2,4-pentanediol were evaporated and dried, followed by calcining, whereby powder c-13 in which the particles I4 were coated with alumina was prepared. 173.4 g of this powder c-13 and 1.6 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were added to the ball mill, and the powder c-13 was milled, whereby slurry c-13 with an average particle diameter of 3 μm was formed.

Next, rhodium nitrate was impregnated into zirconium-lanthanum composite oxide particles with an average particle diameter of 20 nm, and a resultant was calcined at 700° C. for two hours, whereby particles J4 having rhodium supported thereon by 0.814% were prepared. A degree of dispersion of Rh in the particles J4 was 45%. Aluminum isopropoxide equivalent to 90 g of Al₂O₃ was dissolved into 2-methyl-2,4-pentanediol. To a solution thus obtained, 90 g of the particles J4 was added, and water was further added thereto, whereby hydrolysis was performed therefor. The water and organic matter such as the 2-methyl-2,4-pentanediol were evaporated and dried, followed by calcining, whereby powder cb-13 in which the particles J4 were coated with alumina was prepared. A degree of dispersion of Rh in the powder cb-13 was 30%. 172 g of this powder cb-13 and 3 g of boehmite alumina were added to a ball mill. Thereafter, 307.5 g of water and 17.5 g of a 10% nitric acid solution were further added to the ball mill, and the powder cb-13 was milled, whereby slurry cb-13 with an average particle diameter of 3 μm was formed. The slurry c-13 was coated by 141 g/L on a honeycomb carrier (capacity: 0.04 L) having a diameter of ø36 mm and 400 cells with a wall thickness of 6 mils, followed by drying, and thereafter, the slurry cb-13 was coated by 59 g/L thereon, followed by drying. Thereafter, a resultant was calcined at 400° C., whereby a sample of Comparative example 13 was obtained. The obtained sample of Comparative example 13 is a catalyst that individually carries thereon Pt by 0.593 g/L and Rh by 0.236 g/L.

[Evaluation]

The catalysts prepared according to Examples 1 to 28 and Comparative examples 1, 2 and 3 to 13 were used, and five pieces of each were mounted per bank in exhaust portions of a V-engine with a displacement of 3500 cc. A durability test was performed in such a manner that Japanese-domestic regular gasoline was used, a catalyst inlet temperature was set at 650° C., and the engine was operated for 30 hours. Then, a thermal history was inspected. Moreover, each of the catalysts after the durability test was built in a simulation exhaust gas flowing device, simulation exhaust gas with a composition shown in Table 1 was flown through the simulation exhaust gas flowing device, and temperatures at which purification rates for NOx, CO and HC(C₃H₆) became 50% (T50 temperature) were investigated while raising a catalyst temperature at a rate of 30° C./min. Furthermore, a first layer and second layer of each of the catalysts after the durability test were scraped off, and pore volumes of such catalyst layers, which were measured by a gas adsorption method, were inspected.

TABLE 1
REACTION GAS COMPOSITION
NO       1000 ppm
O2       0.60%
H2       0.20%
HC(C3H6) 1665 ppmC
CO       0.60%
CO2      15.50%
H2O      10%
N2       RESIDUE
SPACE VELOCITY: SV = 60000/h

Table 2 shows evaluation results and the pore volumes of the catalyst layers in the respective catalysts of Example 1 to Example 10 and Comparative example 1 and Comparative example 2. Moreover, FIG. 4 shows HC T50 temperatures, at which HC(C₃H₆) purification rates became 50%, for Example 1 to Example 10 and Comparative example 1 and Comparative example 2.

	TABLE 2
	FIRST LAYER	SECOND LAYER
	PRE-			PORE	PRE-
	CIOUS	FIRST	SECOND	VOLUME	CIOUS	FIRST
	METAL	COMPOUND	COMPOUND	(cm3/g)	METAL	COMPOUND
EXAMPLE 1	Pt	CeO2	Al2O3	0.25	Rh	ZrCe
						COMPOSITE
						OXIDE
EXAMPLE 2	Pt	CeO2	Al2O3	0.31	Rh	ZrCe
						COMPOSITE
						OXIDE
EXAMPLE 3	Pt	CeO2	Al2O3	0.33	Rh	ZrCe
						COMPOSITE
						OXIDE
EXAMPLE 4	Pt	CeO2	Al2O3	0.35	Rh	ZrCe
						COMPOSITE
						OXIDE
EXAMPLE 5	Pt	CeO2	Al2O3	0.60	Rh	ZrCe
						COMPOSITE
						OXIDE
EXAMPLE 6	Pt	CeZr	Al2O3	0.24	Rh	ZrCe
		COMPOSITE				COMPOSITE
		OXIDE				OXIDE
EXAMPLE 7	Pt	CeZr	Al2O3	0.30	Rh	ZrCe
		COMPOSITE				COMPOSITE
		OXIDE				OXIDE
EXAMPLE 8	Pt	CeZr	Al2O3	0.32	Rh	ZrCe
		COMPOSITE				COMPOSITE
		OXIDE				OXIDE
EXAMPLE 9	Pd	MANGANESE	Al2O3	0.32	Rh	ZrCe
		ALUMINATE				COMPOSITE
						OXIDE
EXAMPLE 10	Pd	MANGANESE	Al2O3	0.35	Rh	ZrCe
		ALUMINATE				COMPOSITE
						OXIDE
COMPARATIVE	Pt	CeO2	Al2O3	0.22	Rh	ZrCe
EXAMPLE 1						COMPOSITE
						OXIDE
COMPARATIVE	Pt	CeO2	Al2O3	0.65	Rh	ZrCe
EXAMPLE 2						COMPOSITE
						OXIDE
	SECOND LAYER	NOx50%	HC 50%	CO 50%
		PORE	PURIFICATION	PURIFICATION	PURIFICATION
	SECOND	VOLUME	TEMPERATURE	TEMPERATURE	TEMPERATURE
	COMPOUND	(cm3/g)	(° C.)	(° C.)	(° C.)
EXAMPLE 1	Al2O3	0.24	286	284	268
EXAMPLE 2	Al2O3	0.30	284	282	266
EXAMPLE 3	Al2O3	0.32	282	280	264
EXAMPLE 4	Al2O3	0.34	280	278	262
EXAMPLE 5	Al2O3	0.57	278	276	260
EXAMPLE 6	Al2O3	0.24	285	283	266
EXAMPLE 7	Al2O3	0.30	283	281	264
EXAMPLE 8	Al2O3	0.32	281	279	262
EXAMPLE 9	Al2O3	0.30	277	275	260
EXAMPLE 10	Al2O3	0.32	275	273	258
COMPARATIVE	ZrO2	0.19	299	297	293
EXAMPLE 1
COMPARATIVE	Al2O3	0.63	305	303	300
EXAMPLE 2

Comparative example 1 is the catalyst, in which alumina from aluminum isopropoxide is used for the first layer, and zirconia was used for the second layer. In both of the layers, the pore volumes were the smallest among the examples. When the Pt particles after the durability test were observed by a TEM, a particle diameter of the Pt particles was approximately 10 nm, coagulation of the Pt particles was small, and coagulation of the Rh particles was also small. However, catalyst activity was low. This is considered to be because, though the particle diameter of the Pt particles is small, the pore volumes are small, the exhaust gas is difficult to pass through the pores, and the exhaust gas is less likely to reach the Pt particles.

In Comparative example 2, alumina particles with a particle diameter as large as 110 nm are used for the first layer. Therefore, the pore volume also becomes large. When the Pt particles were observed by the TEM for the catalyst after the durability test, a particle diameter of the Pt particles became as large as approximately 20 nm or more, the coagulation of the Pt particles was confirmed, and the coagulation of the CeO2 particles was also observed. This is considered to be because, since the alumina particles are large, gaps among the alumina particles are large, the Pt-attached ceria particles moved from the gaps during the durability test, and the coagulation among the ceria particles occurred. It is also considered that the Pt particles were coagulated following the coagulation of the ceria particles, leading to an increase of the diameter of the Pt particles concerned. In a similar way, an increase of the particle diameter of the. Rh particles in the second layer was observed to 15 nm. It is considered that the catalyst activity therefore became low though the pore volumes were large.

As opposed to this, in each of the catalysts in Example 1 to Example 8, the particle diameter of the Pt particles after the durability test was approximately 10 nm, and the coagulation of the Pt particles was small. Moreover, the particle diameter of the Rh particles was approximately 6 nm, and the coagulation thereof was small. Furthermore, in each of Example 9 and Example 10, the diameter of the Pd particles was as small as 7 nm to 8 nm, and the coagulation of the Pd particles was small. Also with regard to the Rh particles, the diameter thereof was approximately 6 nm, and the coagulation thereof was small. The catalyst activity of each of these Examples 1 to 10 was extremely good in comparison with those of Comparative examples 1 and 2, and high activity was able to be obtained.

Table 3 shows evaluation results and the pore volumes of the catalyst layers in the respective catalysts of Example 11 to Example 16 and Comparative example 3 to Comparative example 6. Moreover, FIG. 5 shows HC T50 temperatures, at which the HC(C₃H₆) purification rates became 50%, for Example 11 to Example 16 and Comparative example 3 to Comparative example 6.

	TABLE 3
	FIRST LAYER	SECOND LAYER
	PRE-			PORE	PRE-
	CIOUS	FIRST	SECOND	VOLUME	CIOUS	FIRST
	METAL	COMPOUND	COMPOUND	(cm3/g)	METAL	COMPOUND
EXAMPLE 11	Pt	CeZr	Al2O3	0.24	Rh	ZrLa
		COMPOSITE				COMPOSITE
		OXIDE				OXIDE
EXAMPLE 12	Pt	CeZr	Al2O3	0.34	Rh	ZrLa
		COMPOSITE				COMPOSITE
		OXIDE				OXIDE
EXAMPLE 13	Pt	CeZr	Al2O3	0.49	Rh	ZrLa
		COMPOSITE				COMPOSITE
		OXIDE				OXIDE
EXAMPLE 14	Pt	CeZr	Al2O3	0.80	Rh	ZrLa
		COMPOSITE				COMPOSITE
		OXIDE				OXIDE
EXAMPLE 15	Pd	CeZr	Al2O3	0.33	Rh	ZrLa
		COMPOSITE				COMPOSITE
		OXIDE				OXIDE
EXAMPLE 16	Pd	CeZr	Al2O3	0.47	Rh	ZrLa
		COMPOSITE				COMPOSITE
		OXIDE				OXIDE
COMPARATIVE	Pt	CeZr	Al2O3	0.21	Rh	ZrLa
EXAMPLE 3		COMPOSITE				COMPOSITE
		OXIDE				OXIDE
COMPARATIVE	Pt	CeZr	Al2O3	0.83	Rh	ZrLa
EXAMPLE 4		COMPOSITE				COMPOSITE
		OXIDE				OXIDE
COMPARATIVE	Pt	CeZr	Al2O3	0.82	Rh	ZrLa
EXAMPLE 5		COMPOSITE				COMPOSITE
		OXIDE				OXIDE
COMPARATIVE	Pt	CeZr	Al2O3	0.22	Rh	ZrLa
EXAMPLE 6		COMPOSITE				COMPOSITE
		OXIDE				OXIDE
	SECOND LAYER	NOx50%	HC 50%	CO 50%
		PORE	PURIFICATION	PURIFICATION	PURIFICATION
	SECOND	VOLUME	TEMPERATURE	TEMPERATURE	TEMPERATURE
	COMPOUND	(cm3/g)	(° C.)	(° C.)	(° C.)
EXAMPLE 11	Al2O3	0.25	323	317	315
EXAMPLE 12	Al2O3	0.33	321	316	314
EXAMPLE 13	Al2O3	0.51	320	314	312
EXAMPLE 14	Al2O3	0.78	317	310	308
EXAMPLE 15	Al2O3	0.32	319	313	310
EXAMPLE 16	Al2O3	0.49	318	314	311
COMPARATIVE	Al2O3	0.22	329	325	321
EXAMPLE 3
COMPARATIVE	Al2O3	0.82	328	326	322
EXAMPLE 4
COMPARATIVE	Al2O3	0.81	328	325	321
EXAMPLE 5
COMPARATIVE	Al2O3	0.22	329	326	322
EXAMPLE 6

Comparative example 3 is the catalyst, in which alumina from aluminum isopropoxide is used for the first layer, and zirconia was used for the second layer. In both of the layers, the pore volumes were the smallest among the examples. When the Pt particles after the durability were observed by the TEM, a particle diameter of the Pt particles was approximately 10 nm, and the coagulation of the Pt particles was small. Moreover, the coagulation of Rh was also small. However, catalyst activity was low. This is considered to be because, though the diameter of the Pt particles is small, the pore volumes are small, the exhaust gas is difficult to pass through the pores, and the exhaust gas is less likely to reach the Pt particles.

In Comparative example 4, alumina particles with a particle diameter as large as 130 nm are used for the first layer. Therefore, the pore volume also takes a large value. When the Pt particles were observed by the TEM for the catalyst after the durability, a diameter of the Pt particles became as large as approximately 20 nm or more, the coagulation of the Pt particles was confirmed, and the coagulation of the cerium-zirconium composite oxide particles was also observed. This is considered to be because, since the alumina particles are large, gaps among the alumina particles are large, the Pt-attached cerium-zirconium composite oxide particles moved from the gaps during the durability, and the coagulation among the cerium-zirconium composite oxide particles occurred. It is also considered that Pt was coagulated following the coagulation of the cerium-zirconium composite oxide particles, leading to an increase of the diameter of the Pt particles concerned. In a similar way, an increase of the particle diameter of the Rh particles in the second layer was observed to 15 nm. It is considered that the catalyst activity therefore became low though the pore volumes were large.

Comparative example 5 is one using, for the source of the alumina, the boehmite in which the aspect ratio is as large as 15, in which the pore volumes are large. When the Pt particles after the durability were observed by the TEM, a diameter of the Pt particles became as large as 20 nm or more, the coagulation of the Pt particles was confirmed, and the coagulation of the cerium-zirconium composite oxide particles was also observed. This is considered to be because, since the alumina particles are long, gaps among the alumina particles become large, the Pt-attached cerium-zirconium composite oxide particles moved from the gaps during the durability, and the coagulation among the cerium-zirconium composite oxide particles occurred. It is also considered that Pt was coagulated following the coagulation of the cerium-zirconium composite oxide particles, leading to an increase of the diameter of the Pt particles concerned. In a similar way, an increase of the particle diameter of the Rh particles in the second layer was observed to 15 nm. It is considered that the catalyst activity therefore became low though the pore volumes were large.

Comparative example 6 is one using, for the source of the alumina, the boehmite in which the aspect ratio is as small as 0.25, in which the pore volumes are small in both of the first layer and the second layer. When the Pt particles after the durability were observed by the TEM, a diameter of the Pt particles was approximately 10 nm, and the coagulation of the Pt particles was small. Moreover, the coagulation of Rh was also small. However, catalyst activity was low. This is considered to be because, though the diameter of the Pt particles is small, the pore volumes are small, the exhaust gas is difficult to pass through the pores, and the exhaust gas is less likely to reach Pt.

As opposed to this, in each of the catalysts in Example 11 to Example 14, the diameter of the Pt particles after the durability was approximately 10 nm, and the coagulation of the Pt particles was small. Moreover, the particle diameter of the Rh particles was approximately 6 nm, and the coagulation thereof was small. Furthermore, in each of Example 15 and Example 16, the diameter of the Pd particles was approximately 6 nm, and the coagulation of the Pd particles was small. Also with regard to the Rh particles, the diameter thereof was approximately 6 nm, and the coagulation thereof was also small. From the above, the catalyst activity of each of these Examples 11 to 16 was extremely good in comparison with those of Comparative examples 3 to 6, and high activity was able to be obtained.

Table 4 shows evaluation results and the pore volumes of the catalyst layers in the respective catalysts of Example 17 to Example 19 and Comparative examples 7 and 8. Moreover, FIG. 6 shows HC T50 temperatures, at which the HC(C₃H₆) purification rates became 50%, for Example 17 to Example 19 and Comparative examples 7 and 8.

	TABLE 4
	FIRST LAYER	SECOND LAYER
		FIRST				FIRST
	PRE-	COMPOUND/		PORE	PRE-	COMPOUND/
	CIOUS	PORE VOLUME	SECOND	VOLUME	CIOUS	PORE VOLUME
	METAL	(cm3/g)	COMPOUND	(cm3/g)	METAL	(cm3/g)
EXAMPLE 17	Pt	CeZr	Al2O3	0.43	Rh	ZrLa
		COMPOSITE				COMPOSITE
		OXIDE 0.18				OXIDE 0.28
EXAMPLE 18	Pt	CeZr	Al2O3	0.47	Rh	ZrLa
		COMPOSITE				COMPOSITE
		OXIDE 0.28				OXIDE 0.30
EXAMPLE 19	Pt	CeZr	Al2O3	0.49	Rh	ZrLa
		COMPOSITE				COMPOSITE
		OXIDE 0.30				OXIDE 0.32
COMPARATIVE	Pt	CeZr	Al2O3	0.20	Rh	ZrLa
EXAMPLE 7		COMPOSITE				COMPOSITE
		OXIDE 0.15				OXIDE 0.16
COMPARATIVE	Pt	CeZr	Al2O3	0.23	Rh	ZrLa
EXAMPLE 8		COMPOSITE				COMPOSITE
		OXIDE 0.40				OXIDE 0.41
	SECOND LAYER	NOx50%	HC 50%	CO 50%
			PORE	PURIFICATION	PURIFICATION	PURIFICATION
		SECOND	VOLUME	TEMPERATURE	TEMPERATURE	TEMPERATURE
		COMPOUND	(cm3/g)	(° C.)	(° C.)	(° C.)
	EXAMPLE 17	Al2O3	0.45	321	316	314
	EXAMPLE 18	Al2O3	0.47	320	314	311
	EXAMPLE 19	Al2O3	0.51	318	312	309
	COMPARATIVE	Al2O3	0.21	328	326	323
	EXAMPLE 7
	COMPARATIVE	Al2O3	0.22	327	323	321
	EXAMPLE 8

Comparative example 7 is one using one, in which the pore volume of the cerium-zirconium composite oxide is 0.15 cm³/g, and the volume of the zirconium-lanthanum composite oxide is 0.16 cm³/g, and catalyst activity thereof was low. Catalyst activity was similarly low also in Comparative example 8. This is considered to be because, since the pore volumes of the cerium-zirconium composite oxide and the zirconium-lanthanum composite oxide are small, the pore volumes of the catalyst layers also became small. As opposed to this, in each of the catalysts in Example 17 to Example 19, the diameter of the Pt particles after the durability was approximately 10 nm, and the coagulation of the Pt particles was small. Moreover, the particle diameter of the Rh particles was approximately 6 nm, and the coagulation thereof was also small. From the above, the catalyst activity of each of these Examples 17 to 19 was extremely good in comparison with those of Comparative examples 7 and 8, and high activity is able to be obtained.

Table 5 shows evaluation results and the pore volumes of the catalyst layers in the respective catalysts of Example 20 to Example 22 and Comparative examples 9 and 10. Moreover, FIG. 7 shows HC T50 temperatures, at which the HC(C₃H₆) purification rates became 50%, for Example 20 to Example 22 and Comparative examples 9 and 10.

	TABLE 5
	FIRST LAYER	SECOND LAYER
		FIRST				FIRST
	PRE-	COMPOUND/		PORE	PRE-	COMPOUND/
	CIOUS	CeO2:ZrO2	SECOND	VOLUME	CIOUS	ZrO2:La2O2
	METAL	(%)	COMPOUND	(cm3/g)	METAL	(%)
EXAMPLE 20	Pt	CeZr	Al2O3	0.49	Rh	ZrLa
		COMPOSITE				COMPOSITE
		OXIDE 74:26				OXIDE 95:5
EXAMPLE 21	Pt	CeZr	Al2O3	0.50	Rh	ZrLa
		COMPOSITE				COMPOSITE
		OXIDE 78:22				OXIDE 97:3
EXAMPLE 22	Pt	CeZr	Al2O3	0.49	Rh	ZrLa
		COMPOSITE				COMPOSITE
		OXIDE 80:10				OXIDE 99:1
COMPARATIVE	Pt	CeZr	Al2O3	0.23	Rh	ZrLa
EXAMPLE 9		COMPOSITE				COMPOSITE
		OXIDE 70:30				OXIDE 90:10
COMPARATIVE	Pt	CeZr	Al2O3	0.22	Rh	ZrLa
EXAMPLE 10		COMPOSITE				COMPOSITE
		OXIDE 90:10				OXIDE 100:0
	SECOND LAYER	NOx50%	HC 50%	CO 50%
		PORE	PURIFICATION	PURIFICATION	PURIFICATION
	SECOND	VOLUME	TEMPERATURE	TEMPERATURE	TEMPERATURE
	COMPOUND	(cm3/g)	(° C.)	(° C.)	(° C.)
EXAMPLE 20	Al2O3	0.51	321	314	309
EXAMPLE 21	Al2O3	0.52	319	313	307
EXAMPLE 22	Al2O3	0.51	321	315	309
COMPARATIVE	Al2O3	0.22	329	326	322
EXAMPLE 9
COMPARATIVE	Al2O3	0.22	329	327	323
EXAMPLE 10

In Comparative example 9 and Comparative example 10, as the first compounds 5, those were used, in which composite ratios of the cerium oxide, the zirconium oxide and the like were changed. In Comparative example 9, the composite ratios of the cerium oxide and the zirconium oxide in the first layer are 70% and 30%, the composite ratios of the zirconium oxide and the lanthanum oxide in the second layer are 90% and 10%, and catalyst activity thereof is low in comparison with those of Examples 20 to 22. In accordance with the observation using the TEM, the diameter of the Pt particles in the first layer was approximately 10 nm. The diameter of the Rh particles in the second layer was as small as approximately 6 nm; however, a state was observed, in which the Rh particles were buried in aggregates of the zirconium-lanthanum composite oxide particles. Moreover, in Comparative example 10, the composite ratios of the cerium oxide and the zirconium oxide in the first layer are 90% and 10%, the zirconium oxide occupied 100% in the second layer, and catalyst activity thereof is low in comparison with those of Examples 20 to 22.

In accordance with the observation using the TEM, the diameter of the Pt particles in the first layer was approximately 10 nm. Although the diameter of the Rh particles in the second layer was as small as approximately 6 nm, the state was observed, in which the Rh particles were buried in the aggregates of the zirconium oxide particles. It is considered that this is caused by the fact that the composite oxide of the cerium oxide and the zirconium oxide is inferior in oxygen evolution capability, as well as that the pore volumes of the catalysts of Comparative examples 9 and 10 are small. Moreover, it is considered that this is caused by the fact that, owing to the composite ratios of the zirconium oxide and the lanthanum oxide, the zirconium-lanthanum composite oxide particles become likely to be coagulated, and the Rh particles are buried in the zirconium-lanthanum composite oxide particles and the zirconium oxide particles, and become difficult to contact the exhaust gas.

Table 6 shows evaluation results and the pore volumes of the catalyst layers in the respective catalysts of Example 23 to Example 25 and Comparative examples 11 and 12. Moreover, FIG. 8 shows HC T50 temperatures, at which the HC(C₃H₆) purification rates became 50%, for Example 23 to Example 25 and Comparative examples 11 and 12.

	TABLE 6
	FIRST LAYER	SECOND LAYER
	PRE-		SECOND	PORE	PRE-
	CIOUS	FIRST	COMPOUND/	VOLUME	CIOUS	FIRST
	METAL	COMPOUND	CeO2:ZrO2	(cm3/g)	METAL	COMPOUND
EXAMPLE 23	Pt	CeZr	Al2O3 5:7	0.27	Rh	ZrLa
		COMPOSITE				COMPOSITE
		OXIDE				OXIDE
EXAMPLE 24	Pt	CeZr	Al2O3 10:5	0.31	Rh	ZrLa
		COMPOSITE				COMPOSITE
		OXIDE				OXIDE
EXAMPLE 25	Pt	CeZr	Al2O3 15:3	0.28	Rh	ZrLa
		COMPOSITE				COMPOSITE
		OXIDE				OXIDE
COMPARATIVE	Pt	CeZr	Al2O3 2:1	0.22	Rh	ZrLa
EXAMPLE 11		COMPOSITE				COMPOSITE
		OXIDE				OXIDE
COMPARATIVE	Pt	CeZr	Al2O3 20:10	0.23	Rh	ZrLa
EXAMPLE 12		COMPOSITE				COMPOSITE
		OXIDE				OXIDE
	SECOND LAYER	NOx50%	HC 50%	CO 50%
		PORE	PURIFICATION	PURIFICATION	PURIFICATION
	SECOND	VOLUME	TEMPERATURE	TEMPERATURE	TEMPERATURE
	COMPOUND	(cm3/g)	(° C.)	(° C.)	(° C.)
EXAMPLE 23	Al2O3	0.26	322	316	316
EXAMPLE 24	Al2O3	0.26	320	315	313
EXAMPLE 25	Al2O3	0.26	321	316	315
COMPARATIVE	Al2O3	0.22	328	326	322
EXAMPLE 11
COMPARATIVE	Al2O3	0.22	328	326	322
EXAMPLE 12

In Comparative examples 11 and 12, catalyst activities thereof are low in comparison with those of Examples 23 to 25. In Examples 23 to 25, the cerium compound and the zirconium compound are added to such an alumina precursor, whereby heat resistance of the alumina after being calcined is enhanced, and the pore volumes after the durability are maintained largely. However, in Comparative examples 11 and 12, there is no effect of adding the cerium compound and the zirconium compound, the pore volumes after the durability cannot be ensured, and the pore volumes become small, and therefore, it is considered that the exhaust gas becomes less likely to reach the precious metals, leading to such a decrease of the catalyst activity.

Table 7 shows evaluation results and the pore volumes of the catalyst layers in the respective catalysts of Example 26 to Example 28 and Comparative example 13. Moreover, FIG. 9 shows HC T50 temperatures, at which the HC(C₃H₆) purification rates became 50%, for Example 26 to Example 28 and Comparative examples 13.

	TABLE 7
	FIRST LAYER	SECOND LAYER
	PRE-			PORE	PRE-
	CIOUS	FIRST	SECOND	VOLUME	CIOUS	FIRST
	METAL	COMPOUND	COMPOUND	(cm3/g)	METAL	COMPOUND
EXAMPLE 26	Pt	CeZr	Al2O3	0.49	Rh	ZrLa
		COMPOSITE				COMPOSITE
		OXIDE				OXIDE
EXAMPLE 27	Pt	CeZr	Al2O3	0.49	Rh	ZrLa
		COMPOSITE				COMPOSITE
		OXIDE				OXIDE
EXAMPLE 28	Pt	CeZr	Al2O3	0.49	Rh	ZrLa
		COMPOSITE				COMPOSITE
		OXIDE				OXIDE
COMPARATIVE	Pt	CeZr	Al2O3	0.22	Rh	ZrLa
EXAMPLE 13		COMPOSITE				COMPOSITE
		OXIDE				OXIDE
	SECOND LAYER	NOx50%	HC 50%	CO 50%
		PORE	PURIFICATION	PURIFICATION	PURIFICATION
	SECOND	VOLUME	TEMPERATURE	TEMPERATURE	TEMPERATURE
	COMPOUND	(cm3/g)	(° C.)	(° C.)	(° C.)
EXAMPLE 26	Al2O3	0.50	324	318	315
EXAMPLE 27	Al2O3	0.50	322	315	312
EXAMPLE 28	Al2O3	0.50	320	311	309
COMPARATIVE	Al2O3	0.22	330	328	325
EXAMPLE 13

In Comparative example 13, catalyst activity thereof is low in comparison with those of Examples 26 to 28. In Examples 26 to 28, the diameter of the Pt particles in the first layer was approximately 10 nm or less in accordance with the observation using the TEM. The diameter of the Rh particles in the second layer was as small as approximately 6 nm or less. This is considered to be because the initial degrees of dispersion of the precious metal particles were high and effects of the precious metals lasted even after the durability. As opposed to this, in Comparative example 13, the diameter of the Pt particles in the first layer was approximately 15 nm in accordance with the observation using the TEM. The diameter of the Rh particles in the second layer was approximately 10 nm, and the particle diameters became somewhat larger in comparison with those of Examples 26 to 28. This is considered to be because the initial degrees of dispersion of the precious metals were low and the coagulation of the precious metal particles owing to the durability became likely to progress.

INDUSTRIAL APPLICABILITY

The present invention can be applied to the exhaust gas purifying catalyst that purifies the exhaust gas discharged from a vehicle such as an automobile.

Claims

1. An exhaust gas purifying catalyst, comprising:

a honeycomb carrier; and

a catalyst layer provided on the honeycomb carrier, the catalyst layer comprising: precious metal particles; a plurality of first compounds on which the precious metal particles are supported; and second compounds which cover the plurality of first compounds on which the precious metal particles are supported and separate the first compounds from one another,

wherein a pore volume of the catalyst layer is within a range of 0.24 to 0.8 cm3/g.

2. The exhaust gas purifying catalyst according to claim 1, wherein the first compounds are an oxide containing Ce.

3. The exhaust gas purifying catalyst according to claim 1, wherein the first compounds contain CeO2.

4. The exhaust gas purifying catalyst according to claim 1, wherein the first compounds contain a composite oxide of Ce and Zr.

5. The exhaust gas purifying catalyst according to claim 1, wherein the second compounds comprises Al2O3.

6. The exhaust gas purifying catalyst according to claim 1, wherein the second compounds are an oxide containing at least either of Al and Zr.

7. The exhaust gas purifying catalyst according to claim 1, wherein both of the first compounds and the second compounds are formed into a particle shape, and an average particle diameter of the second compounds is 10 to 100 nm.

8. The exhaust gas purifying catalyst according to claim 1, wherein the precious metal particles comprises at least one selected from the group consisting of Pt, Pd and Rh.

9. The exhaust gas purifying catalyst according to claim 1, wherein the pore volume of the first compounds is within a range of 0.18 to 0.38 cm3/g.

10. The exhaust gas purifying catalyst according to claim 1, wherein the first compounds are composed of CeO2 that occupies 74 to 80% and ZrO2 that occupies 20 to 26%.

11. The exhaust gas purifying catalyst according to claim 1, wherein the first compounds are composed of ZrO2 that occupies 95 to 99% and La2O3 that occupies 1 to 5%.

12. The exhaust gas purifying catalyst according to claim 1, wherein a pore volume of a precursor of the second compounds after being calcined is within a range of 0.8 to 1.0 cm3/g.

13. The exhaust gas purifying catalyst according to claim 5, wherein the alumina comprises CeO2 that occupies 5 to 15% and ZrO2 that occupies 3 to 7%.

14. The exhaust gas purifying catalyst according to claim 1, wherein an aspect ratio of the precursor of the second compounds is within a range of 0.5 to 10.

15. The exhaust gas purifying catalyst according to claim 1,

wherein the second compounds comprise Al2O3 derived from boehmite of which an aspect ratio is within a range of 0.5 to 10.

16. The exhaust gas purifying catalyst according to claim 1, wherein a degree of dispersion of the precious metal particles in powder of the exhaust gas purifying catalyst is within a range of 35 to 80%.

17. The exhaust gas purifying catalyst according to claim 1, wherein a degree of dispersion of the precious metal particles supported on the first compounds is within a range of 50 to 100%.