JP2005305363A - Catalyst for cleaning exhaust gas - Google Patents
Catalyst for cleaning exhaust gas Download PDFInfo
- Publication number
- JP2005305363A JP2005305363A JP2004128626A JP2004128626A JP2005305363A JP 2005305363 A JP2005305363 A JP 2005305363A JP 2004128626 A JP2004128626 A JP 2004128626A JP 2004128626 A JP2004128626 A JP 2004128626A JP 2005305363 A JP2005305363 A JP 2005305363A
- Authority
- JP
- Japan
- Prior art keywords
- catalyst
- exhaust gas
- powder
- metal
- oxide
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000003054 catalyst Substances 0.000 title claims abstract description 153
- 238000004140 cleaning Methods 0.000 title abstract 2
- 239000006104 solid solution Substances 0.000 claims abstract description 30
- 229910052751 metal Inorganic materials 0.000 claims abstract description 23
- 239000002184 metal Substances 0.000 claims abstract description 22
- 238000011144 upstream manufacturing Methods 0.000 claims abstract description 14
- CETPSERCERDGAM-UHFFFAOYSA-N ceric oxide Chemical compound O=[Ce]=O CETPSERCERDGAM-UHFFFAOYSA-N 0.000 claims abstract description 13
- 229910000422 cerium(IV) oxide Inorganic materials 0.000 claims abstract description 13
- 229910052777 Praseodymium Inorganic materials 0.000 claims abstract description 11
- 229910052742 iron Inorganic materials 0.000 claims abstract description 10
- 229910052709 silver Inorganic materials 0.000 claims abstract description 10
- 229910052726 zirconium Inorganic materials 0.000 claims abstract description 7
- 239000002131 composite material Substances 0.000 claims description 19
- 238000000746 purification Methods 0.000 claims description 17
- 239000000203 mixture Substances 0.000 abstract description 26
- 229910000510 noble metal Inorganic materials 0.000 abstract description 13
- 230000000694 effects Effects 0.000 abstract description 8
- 239000000243 solution Substances 0.000 abstract description 5
- 229910052723 transition metal Inorganic materials 0.000 abstract description 4
- 150000003624 transition metals Chemical class 0.000 abstract description 4
- 150000001875 compounds Chemical class 0.000 abstract 1
- 238000000151 deposition Methods 0.000 abstract 1
- 230000001590 oxidative effect Effects 0.000 abstract 1
- 239000000843 powder Substances 0.000 description 71
- 230000000052 comparative effect Effects 0.000 description 22
- 238000007254 oxidation reaction Methods 0.000 description 22
- 239000000758 substrate Substances 0.000 description 22
- 230000003647 oxidation Effects 0.000 description 20
- 239000002002 slurry Substances 0.000 description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 13
- 229910002492 Ce(NO3)3·6H2O Inorganic materials 0.000 description 9
- 229910006219 ZrO(NO3)2·2H2O Inorganic materials 0.000 description 9
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 9
- 238000005342 ion exchange Methods 0.000 description 9
- 101710134784 Agnoprotein Proteins 0.000 description 8
- 229910002554 Fe(NO3)3·9H2O Inorganic materials 0.000 description 8
- 230000010718 Oxidation Activity Effects 0.000 description 8
- 239000002244 precipitate Substances 0.000 description 8
- 230000004913 activation Effects 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- OMOVVBIIQSXZSZ-UHFFFAOYSA-N [6-(4-acetyloxy-5,9a-dimethyl-2,7-dioxo-4,5a,6,9-tetrahydro-3h-pyrano[3,4-b]oxepin-5-yl)-5-formyloxy-3-(furan-3-yl)-3a-methyl-7-methylidene-1a,2,3,4,5,6-hexahydroindeno[1,7a-b]oxiren-4-yl] 2-hydroxy-3-methylpentanoate Chemical compound CC12C(OC(=O)C(O)C(C)CC)C(OC=O)C(C3(C)C(CC(=O)OC4(C)COC(=O)CC43)OC(C)=O)C(=C)C32OC3CC1C=1C=COC=1 OMOVVBIIQSXZSZ-UHFFFAOYSA-N 0.000 description 6
- 239000010948 rhodium Substances 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 239000000446 fuel Substances 0.000 description 4
- 239000008188 pellet Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 235000011114 ammonium hydroxide Nutrition 0.000 description 3
- 229910002091 carbon monoxide Inorganic materials 0.000 description 3
- 229910052878 cordierite Inorganic materials 0.000 description 3
- JSKIRARMQDRGJZ-UHFFFAOYSA-N dimagnesium dioxido-bis[(1-oxido-3-oxo-2,4,6,8,9-pentaoxa-1,3-disila-5,7-dialuminabicyclo[3.3.1]nonan-7-yl)oxy]silane Chemical compound [Mg++].[Mg++].[O-][Si]([O-])(O[Al]1O[Al]2O[Si](=O)O[Si]([O-])(O1)O2)O[Al]1O[Al]2O[Si](=O)O[Si]([O-])(O1)O2 JSKIRARMQDRGJZ-UHFFFAOYSA-N 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 229910004631 Ce(NO3)3.6H2O Inorganic materials 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000006228 supernatant Substances 0.000 description 2
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- 229910000608 Fe(NO3)3.9H2O Inorganic materials 0.000 description 1
- 230000010757 Reduction Activity Effects 0.000 description 1
- 229910008337 ZrO(NO3)2.2H2O Inorganic materials 0.000 description 1
- 150000004703 alkoxides Chemical class 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- IXSUHTFXKKBBJP-UHFFFAOYSA-L azanide;platinum(2+);dinitrite Chemical compound [NH2-].[NH2-].[Pt+2].[O-]N=O.[O-]N=O IXSUHTFXKKBBJP-UHFFFAOYSA-L 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000000975 co-precipitation Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- -1 for example Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000006263 metalation reaction Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 239000010970 precious metal Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- VXNYVYJABGOSBX-UHFFFAOYSA-N rhodium(3+);trinitrate Chemical compound [Rh+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O VXNYVYJABGOSBX-UHFFFAOYSA-N 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
Images
Landscapes
- Exhaust Gas Treatment By Means Of Catalyst (AREA)
- Catalysts (AREA)
- Exhaust Gas After Treatment (AREA)
Abstract
Description
本発明は自動車の排ガス浄化用触媒に関し、詳しくはきわめて高い酸化活性を示す安価な触媒に関する。 The present invention relates to an exhaust gas purification catalyst for automobiles, and more particularly to an inexpensive catalyst exhibiting extremely high oxidation activity.
従来より自動車の排ガス浄化用触媒として、アルミナなどの多孔質担体にPtなどの貴金属を担持した酸化触媒が用いられている。この酸化触媒では、排ガス中のHC及びCOが酸化されて浄化される。 Conventionally, an oxidation catalyst in which a noble metal such as Pt is supported on a porous carrier such as alumina has been used as an exhaust gas purification catalyst for automobiles. With this oxidation catalyst, HC and CO in the exhaust gas are oxidized and purified.
また、アルミナなどの多孔質担体にPtなどの貴金属を担持した触媒は、空燃比を理論空燃比に制御することで排ガス中のCO及びHCの酸化とNOx の還元とを同時に行うため、三元触媒と称されている。このような三元触媒としては、例えばコーディエライトなどからなる耐熱性のハニカム基材にγ−アルミナからなる多孔質担体層を形成し、その多孔質担体層にPt、Rhなどの貴金属を担持させたものが広く用いられている。 In addition, a catalyst in which a noble metal such as Pt is supported on a porous carrier such as alumina simultaneously performs oxidation of CO and HC in exhaust gas and reduction of NO x by controlling the air-fuel ratio to the theoretical air-fuel ratio. It is called the original catalyst. As such a three-way catalyst, a porous carrier layer made of γ-alumina is formed on a heat-resistant honeycomb substrate made of cordierite, for example, and a noble metal such as Pt or Rh is supported on the porous carrier layer. The ones used are widely used.
しかしながら酸化触媒及び三元触媒では、担持されている貴金属がその活性化温度以上となるまでは触媒反応が生じないという問題がある。そのためエンジン始動時あるいは冷間時などには、排ガスの温度が低いために貴金属が活性化温度に達せず、HCやNOx の浄化は困難である。 However, the oxidation catalyst and the three-way catalyst have a problem that the catalytic reaction does not occur until the supported noble metal becomes higher than its activation temperature. Therefore, such as during between engine start-up or cold is a noble metal in the temperature of the exhaust gas is low does not reach the activation temperature, the purification of HC and NO x is difficult.
またエンジンが冷間状態にある場合には、通常の運転時より燃料濃度の高い混合気が供給されるため、排ガス中に含まれるHC量が多い。さらに貴金属は、約 300℃以上にならないと活性化せず、始動時など排ガス温度が低い場合には排ガス中のHCを十分に浄化することができない。このためエンジンの冷間時や始動時などには、HCを特に効率よく浄化することが望まれている。 Further, when the engine is in a cold state, an air-fuel mixture having a higher fuel concentration than that during normal operation is supplied, so that the amount of HC contained in the exhaust gas is large. Furthermore, noble metals will not be activated unless the temperature exceeds about 300 ° C, and HC in the exhaust gas cannot be sufficiently purified if the exhaust gas temperature is low, such as during startup. For this reason, it is desired to purify HC particularly efficiently when the engine is cold or started.
そこでエンジン直下に酸化触媒を配置し、その排ガス下流側に三元触媒を配置することが行われている。エンジン直下に配置された酸化触媒には高温の排ガスが流入するので、担持されている貴金属の活性化温度まで速やかに昇温される。そして活性化温度以上ではHCやCOの酸化反応が生じ、その反応熱によって排ガスの温度が上昇するので、三元触媒に流入する排ガスの温度も上昇し、三元触媒も活性化温度まで容易に昇温される。したがって三元触媒の暖機までの時間が短縮され、HCなどの排出を抑制することができる。 Therefore, an oxidation catalyst is disposed directly under the engine, and a three-way catalyst is disposed downstream of the exhaust gas. Since high-temperature exhaust gas flows into the oxidation catalyst disposed directly under the engine, the temperature is quickly raised to the activation temperature of the noble metal supported. Above the activation temperature, oxidation reactions of HC and CO occur, and the temperature of the exhaust gas rises due to the reaction heat, so the temperature of the exhaust gas flowing into the three-way catalyst also rises, and the three-way catalyst can easily reach the activation temperature. The temperature is raised. Therefore, the time until the three-way catalyst is warmed up is shortened, and the discharge of HC and the like can be suppressed.
しかしながら従来の酸化触媒では、Ptなどの貴金属を担持しているために、高価であるという問題がある。そこで例えば特開2001−239161号公報などに開示されているように、貴金属の中でも安価なAg、あるいはFeなどの遷移金属を用いることも提案されている。しかしそのような触媒は、安価ではあるもののPtを担持した触媒に比べて酸化活性が著しく低いという不具合がある。したがってAgや遷移金属は、Ptなどの貴金属を補助するものとして用いられているのが現状である。
本発明は上記した事情に鑑みてなされたものであり、高価な貴金属を用いずに安価な触媒とするとともに、Ptなどには及ばずとも十分な酸化活性を発現できるようにすることを目的とする。 The present invention has been made in view of the circumstances described above, and aims to provide an inexpensive catalyst without using an expensive noble metal, and to allow sufficient oxidation activity to be exhibited even if it does not reach Pt or the like. To do.
上記課題を解決する本発明の排ガス浄化用触媒の特徴は、セリアと、Zr及びFeから選ばれる少なくとも一種の元素の金属又は酸化物と、Ag及びPrから選ばれる少なくとも一種の元素の金属又は酸化物と、を固溶してなる複合酸化物を含むことにある。 The feature of the exhaust gas purifying catalyst of the present invention that solves the above problems is ceria, a metal or oxide of at least one element selected from Zr and Fe, and a metal or oxidation of at least one element selected from Ag and Pr. And a composite oxide formed by solid solution.
複合酸化物は、少なくともZrの金属又は酸化物を固溶しているか、少なくともAgの金属又は酸化物を固溶しているか、あるいは少なくともFeの金属又は酸化物を固溶していることが望ましい。 It is desirable that the composite oxide has at least a Zr metal or oxide in solid solution, at least an Ag metal or oxide in solid solution, or at least an Fe metal or oxide in solid solution. .
また上記複合酸化物は、三元触媒の排ガス上流側に配置されていることが望ましい。 Moreover, it is desirable that the complex oxide is disposed on the exhaust gas upstream side of the three-way catalyst.
本発明の排ガス浄化用触媒によれば、安価なAg、あるいはFeなどの遷移金属を担持した従来の触媒に比べてCO及びHCの酸化活性が格段に高いので、始動時などの低温域におけるエミッションが向上する。また三元触媒の上流に配置することで、三元触媒の暖機性が向上し始動時などの低温域におけるエミッションがさらに向上する。そしてPtなど高価な貴金属を用いていないので、安価な触媒とすることができる。 According to the exhaust gas purifying catalyst of the present invention, the oxidation activity of CO and HC is remarkably higher than that of a conventional catalyst supporting a cheap transition metal such as Ag or Fe. Will improve. Moreover, by arranging upstream of the three-way catalyst, the warm-up property of the three-way catalyst is improved, and the emission in a low temperature region such as at the start is further improved. Since no expensive precious metal such as Pt is used, an inexpensive catalyst can be obtained.
本発明の排ガス浄化用触媒は、セリアと、Zr及びFeから選ばれる少なくとも一種の元素の金属又は酸化物と、Ag及びPrから選ばれる少なくとも一種の元素の金属又は酸化物と、を固溶してなる複合酸化物を含んでいる。以下、Zr及びFeから選ばれる少なくとも一種の元素の金属又は酸化物を「物質Ａ」といい、Ag及びPrから選ばれる少なくとも一種の元素の金属又は酸化物を「物質Ｂ」という。 The exhaust gas purifying catalyst of the present invention comprises a solid solution of ceria, a metal or oxide of at least one element selected from Zr and Fe, and a metal or oxide of at least one element selected from Ag and Pr. A composite oxide. Hereinafter, the metal or oxide of at least one element selected from Zr and Fe is referred to as “substance A”, and the metal or oxide of at least one element selected from Ag and Pr is referred to as “substance B”.
セリアについては、複合酸化物中のセリアの含有量は、全金属元素中のCe量として30モル％以上であることが好ましい。また「物質Ａ」については、複合酸化物中のZr含有量は40モル％以下、Fe含有量は35モル％以下とすることが望ましい。ZrあるいはFeの含有量がこれより多くなると、酸化活性が低下するようになる。 As for ceria, the content of ceria in the composite oxide is preferably 30 mol% or more as the amount of Ce in all metal elements. Regarding “Substance A”, it is desirable that the Zr content in the composite oxide is 40 mol% or less and the Fe content is 35 mol% or less. When the content of Zr or Fe is higher than this, the oxidation activity is lowered.
「物質Ｂ」については、複合酸化物中のAg含有量は40モル％以下、Pr含有量は10モル％以下とすることが望ましい。AgあるいはPrの含有量がこれより多くても効果が飽和し、セリア及び物質Ａの含有量が相対的に低下するため、酸化活性が低下するようになる。 As for “Substance B”, the Ag content in the composite oxide is preferably 40 mol% or less, and the Pr content is preferably 10 mol% or less. Even if the content of Ag or Pr is larger than this, the effect is saturated, and the contents of ceria and substance A are relatively lowered, so that the oxidation activity is lowered.
複合酸化物は、セリアと、「物質Ａ」及び「物質Ｂ」が固溶してなる。「物質Ａ」及び「物質Ｂ」は、金属として固溶していても、酸化物として固溶していてもよい。これらの固溶は、セリアと、「物質Ａ」及び「物質Ｂ」がほぼ均一に固溶していることが好ましい。 The composite oxide is formed by dissolving ceria, “substance A”, and “substance B”. “Substance A” and “Substance B” may be in solid solution as a metal or in the form of an oxide. In these solid solutions, it is preferable that ceria and “substance A” and “substance B” are substantially uniformly dissolved.
本発明の触媒は、この複合酸化物のみから構成することが望ましいが、この複合酸化物の粉末とアルミナ、チタニア、ジルコニアなど他の酸化物の粉末を混合して用いてもよい。また他の酸化物に触媒金属を担持した触媒粉末を混合することもできる。 The catalyst of the present invention is preferably composed only of this composite oxide, but this composite oxide powder and other oxide powders such as alumina, titania and zirconia may be mixed and used. In addition, catalyst powder in which a catalyst metal is supported on another oxide can be mixed.
従来の触媒は、セリア、アルミナなどの多孔質酸化物粉末に触媒金属を担持しているので、触媒粉末の各粒子においては触媒金属は表面ほど多く内部ほど少ない分布をもっている。しかし本発明では、触媒粉末の各粒子は、セリアと「物質Ａ」と「物質Ｂ」とが固溶してなる複合酸化物から主として構成されるので、粒子内部に各金属元素がほぼ均一に含まれ、表面から内部までほぼ同一組成である。このように構成することで、理由は不明であるが高い酸化活性が発現される。またNOx の還元活性も有している。なお表面から内部までほぼ同一組成であることは、ＸＲＦとＸＰＳの分析結果がほぼ同等であることで確認することができる。 In the conventional catalyst, a catalyst metal is supported on a porous oxide powder such as ceria or alumina. Therefore, in each particle of the catalyst powder, the catalyst metal is distributed more on the surface and on the inside. However, in the present invention, each particle of the catalyst powder is mainly composed of a composite oxide in which ceria, “substance A”, and “substance B” are in solid solution. It is contained and has almost the same composition from the surface to the inside. By comprising in this way, a high oxidation activity is expressed although a reason is unknown. It also has NO x reduction activity. In addition, it can confirm that it is the substantially same composition from the surface to the inside because the analysis result of XRF and XPS is substantially equivalent.
本発明にいう複合酸化物を調製するには、可溶性Ce塩と、Zr及びFeから選ばれる少なくとも一種の元素の可溶性塩と、Ag及びPrから選ばれる少なくとも一種の元素の可溶性塩と、の混合水溶液から共沈法によって前駆体を沈殿させ、それを焼成することで複合酸化物を形成することができる。また各元素のアルコキシドの混合物を加水分解し、それを焼成してもよい。 To prepare the composite oxide according to the present invention, a mixture of a soluble Ce salt, a soluble salt of at least one element selected from Zr and Fe, and a soluble salt of at least one element selected from Ag and Pr. A complex oxide can be formed by precipitating a precursor from an aqueous solution by a coprecipitation method and firing it. Alternatively, a mixture of alkoxides of each element may be hydrolyzed and fired.
なお上記複合酸化物では、比表面積が20m2／ｇ以上であることが望ましい比表面積がこれより小さいと、酸化活性が低く実用的でない。 In the above complex oxide, if the specific surface area is desirably 20 m 2 / g or more, the oxidation activity is low and impractical if the specific surface area is smaller than this.
本発明の排ガス浄化用触媒は、ペレット形状としてもよいし、担体基材と、担体基材の表面に形成された触媒層とからなるものとすることもできる。担体基材としては、ハニカム基材、フォーム基材などコージェライトなどの耐熱性セラミックスから形成されたもの、メタル箔から形成されたものを用いることができる。 The exhaust gas purifying catalyst of the present invention may be in the form of pellets, or may be composed of a carrier substrate and a catalyst layer formed on the surface of the carrier substrate. As the carrier substrate, those formed from heat-resistant ceramics such as cordierite such as honeycomb substrate and foam substrate, and those formed from metal foil can be used.
本発明の触媒は、単独でも酸化触媒として用いることができる。また請求項５のように、三元触媒の上流側に上記複合酸化物を配置することが好ましい。この場合、下流側は従来用いられている三元触媒とすることができる。上記複合酸化物を配置した上流側と、従来の三元触媒からなる下流側との構成比率は、体積比で上流側：下流側＝１：５〜５：１の範囲とするのが好ましい。上流側の比率がこの範囲より小さいと低温域における浄化活性が低下し、上流側の比率がこの範囲より大きくなると三元活性が低下する。 The catalyst of the present invention can be used alone or as an oxidation catalyst. Further, as in claim 5, it is preferable to dispose the composite oxide upstream of the three-way catalyst. In this case, the downstream side can be a conventionally used three-way catalyst. The composition ratio between the upstream side where the composite oxide is disposed and the downstream side made of a conventional three-way catalyst is preferably in the range of upstream side: downstream side = 1: 5 to 5: 1 in volume ratio. If the ratio on the upstream side is smaller than this range, the purification activity in the low temperature range is lowered, and if the ratio on the upstream side is larger than this range, the three-way activity is lowered.
上記複合酸化物を三元触媒の上流側に配置した場合には、上流側には高温の排ガスが流入するので、触媒金属の活性化温度まで速やかに昇温される。そして活性化温度以上ではHCやCOの酸化反応が生じ、その反応熱によって排ガスの温度が上昇するので、下流側に流入する排ガスの温度も上昇し、従来の三元触媒であっても活性化温度まで容易に昇温される。したがって暖機までの時間が短縮され、HCなどの排出を抑制することができる。 When the composite oxide is arranged on the upstream side of the three-way catalyst, high temperature exhaust gas flows into the upstream side, so that the temperature is rapidly raised to the activation temperature of the catalyst metal. Above the activation temperature, the oxidation reaction of HC and CO occurs, and the temperature of the exhaust gas rises due to the reaction heat, so the temperature of the exhaust gas flowing into the downstream also rises, and even the conventional three-way catalyst is activated The temperature is easily raised to the temperature. Therefore, the time until warm-up is shortened, and discharge of HC and the like can be suppressed.
以下、実施例及び比較例により本発明を具体的に説明する。 Hereinafter, the present invention will be specifically described with reference to Examples and Comparative Examples.
（実施例１）
AgNO3を17.0ｇと、Fe(NO3)3・9H2Oを40.4ｇと、Ce(NO3)3・6H2Oを62.1ｇと、 ZrO(NO3)2・2H2Oを26.7ｇとを秤量し、 300ccのイオン交換水中に溶解して混合水溶液を調製した。この混合水溶液に、pHが９になるまでNaOH水溶液を滴下し、沈殿物を得た。これを遠心分離器にかけて上澄み液を除去し、80℃のイオン交換水を 150cc加えて遠心分離後に上澄み液を除去する洗浄工程を４回行い、Naイオンを除去した。
(Example 1)
AgNO 3 17.0g, Fe (NO 3 ) 3 · 9H 2 O 40.4g, Ce (NO 3 ) 3 · 6H 2 O 62.1g, ZrO (NO 3 ) 2 · 2H 2 O 26.7g Were weighed and dissolved in 300 cc of ion exchange water to prepare a mixed aqueous solution. To this mixed aqueous solution, an aqueous NaOH solution was added dropwise until the pH reached 9 to obtain a precipitate. The supernatant was removed by centrifuging the solution, 150 cc of ion exchange water at 80 ° C. was added 150 cc, and the supernatant was removed after centrifugation to remove Na ions four times.
得られた沈殿物を 120℃で12時間乾燥し、さらに 500℃で２時間焼成して触媒粉末を得た。この触媒粉末の比表面積は52.6m2／ｇであった。またこの触媒粉末は、表面から内部まで元素組成がほぼ同一である。次いでこの触媒粉末をＣＩＰ（加圧型成形機）で固め、約１mmに粉砕してペレット触媒を調製した。 The obtained precipitate was dried at 120 ° C. for 12 hours and further calcined at 500 ° C. for 2 hours to obtain a catalyst powder. The specific surface area of this catalyst powder was 52.6 m 2 / g. This catalyst powder has almost the same elemental composition from the surface to the inside. Next, this catalyst powder was hardened with a CIP (pressure molding machine) and pulverized to about 1 mm to prepare a pellet catalyst.
（比較例１）
Ce(NO3)3・6H2Oを62.1ｇと、 ZrO(NO3)2・2H2Oを26.7ｇ秤量し、 500ccのイオン交換水中に溶解して混合水溶液を調製した。この混合水溶液に、pHが10になるまでアンモニア水を滴下し、沈殿物を得た。これを実施例１と同様にして濾過・洗浄し、得られた沈殿物を 120℃で12時間乾燥し、さらに 500℃で２時間焼成した後、乳鉢で粉砕してCeO2−ZrO2固溶体粉末を調製した。
(Comparative Example 1)
62.1 g of Ce (NO 3 ) 3 .6H 2 O and 26.7 g of ZrO (NO 3 ) 2 .2H 2 O were weighed and dissolved in 500 cc of ion exchange water to prepare a mixed aqueous solution. Aqueous ammonia was added dropwise to the mixed aqueous solution until the pH reached 10, and a precipitate was obtained. This was filtered and washed in the same manner as in Example 1. The resulting precipitate was dried at 120 ° C. for 12 hours, further calcined at 500 ° C. for 2 hours, and then pulverized in a mortar to obtain CeO 2 —ZrO 2 solid solution powder. Was prepared.
次にAgNO3を17.0ｇと、Fe(NO3)3・9H2Oを40.4ｇとを秤量し、 300ccのイオン交換水中に溶解した。これに上記CeO2−ZrO2固溶体粉末を26.3ｇ投入し、撹拌しながらホットプレートで蒸発・乾固し、さらに 500℃で２時間焼成して触媒粉末を得た。この触媒粉末の比表面積は34.2m2／ｇであった。またこの触媒粉末では、Ag及びFe元素は、表面に多く内部に少ない分布を有している。次いでこの触媒粉末をＣＩＰ（加圧型成形機）で固め、約１mmに粉砕してペレット触媒を調製した。 Next, 17.0 g of AgNO 3 and 40.4 g of Fe (NO 3 ) 3 .9H 2 O were weighed and dissolved in 300 cc of ion exchange water. 26.3 g of the CeO 2 —ZrO 2 solid solution powder was added thereto, evaporated and dried on a hot plate with stirring, and further calcined at 500 ° C. for 2 hours to obtain a catalyst powder. The specific surface area of this catalyst powder was 34.2 m 2 / g. In this catalyst powder, Ag and Fe elements have a large distribution on the surface and a small distribution inside. Next, this catalyst powder was hardened with a CIP (pressure molding machine) and pulverized to about 1 mm to prepare a pellet catalyst.
＜試験例１＞ <Test Example 1>
図１から、実施例１の触媒の方が高い浄化率を示していることがわかり、これは触媒粉末を構成する各元素が表面から内部まで均一に分布した効果であることが明らかである。 From FIG. 1, it can be seen that the catalyst of Example 1 shows a higher purification rate, and it is clear that this is an effect in which each element constituting the catalyst powder is uniformly distributed from the surface to the inside.
（実施例２）
図２に本実施例の触媒を示す。この触媒は、ハニカム基材１と、上流側部分に形成された酸化触媒部２と、酸化触媒部２を除く下流側部分に形成された三元触媒部３とから構成されている。
(Example 2)
FIG. 2 shows the catalyst of this example. This catalyst is composed of a honeycomb substrate 1, an oxidation catalyst portion 2 formed in an upstream portion, and a three-way catalyst portion 3 formed in a downstream portion excluding the oxidation catalyst portion 2.
実施例１で調製された触媒粉末と、アルミナゾル（固形分10重量％）とを、固形分比で触媒粉末：アルミナゾル＝９：１の比率で混合し、適量の水を加えてボールミルにて２時間混合して上流側スラリーを調製した。
The catalyst powder prepared in Example 1 and alumina sol (
そして直径30mm、長さ50mm、６ミル、 400セル／in2 の四角セルをもつコージェライト製ハニカム基材１を用意し、上流側スラリーを一端面から12.5mmの範囲に付着させた後、 250℃で２時間乾燥し、酸化触媒部２を形成した。酸化触媒部２に形成された触媒層のコート量は1.69ｇであり、ハニカム基材１の１Ｌあたり48.3ｇである。 Then, a cordierite honeycomb substrate 1 having a square cell of 30 mm in diameter, 50 mm in length, 6 mil, and 400 cells / in 2 was prepared, and after the upstream slurry was attached within a range of 12.5 mm from one end face, 250 The mixture was dried at 0 ° C. for 2 hours to form an oxidation catalyst part 2. The coating amount of the catalyst layer formed on the oxidation catalyst part 2 is 1.69 g, and 48.3 g per liter of the honeycomb substrate 1.
次にCe(NO3)3・6H2Oを73.165ｇと、 ZrO(NO3)2・2H2Oを 41.16ｇと、 Y(NO3)3・6H2Oを6.48ｇとを秤量し、 300ccのイオン交換水中に溶解して混合水溶液を調製した。この混合水溶液に、pHが９になるまでアンモニア水を滴下し、沈殿物を得た。これを実施例１と同様にして濾過・洗浄し、得られた沈殿物を 120℃で12時間乾燥し、さらに 700℃で２時間焼成してCeO2−ZrO2−Y2O3固溶体粉末を調製した。 Next, we weighed 73.165 g of Ce (NO 3 ) 3 · 6H 2 O, 41.16 g of ZrO (NO 3 ) 2 · 2H 2 O, and 6.48 g of Y (NO 3 ) 3 · 6H 2 O, A mixed aqueous solution was prepared by dissolving in 300 cc of ion exchange water. Ammonia water was added dropwise to the mixed aqueous solution until the pH reached 9, and a precipitate was obtained. This was filtered and washed in the same manner as in Example 1, and the resulting precipitate was dried at 120 ° C. for 12 hours and further calcined at 700 ° C. for 2 hours to obtain CeO 2 —ZrO 2 —Y 2 O 3 solid solution powder. Prepared.
このCeO2−ZrO2−Y2O3固溶体粉末50ｇを 300ccのイオン交換水に分散し、Ptとして 4.4重量％含有するジニトロジアンミン白金溶液を 11.36ｇ添加して２時間撹拌した。その後 120℃で蒸発・乾固し、 500℃で２時間焼成してPtを１重量％担持したPt触媒粉末を調製した。 50 g of this CeO 2 —ZrO 2 —Y 2 O 3 solid solution powder was dispersed in 300 cc of ion exchange water, and 11.36 g of a dinitrodiammine platinum solution containing 4.4 wt% as Pt was added and stirred for 2 hours. Thereafter, it was evaporated and dried at 120 ° C. and calcined at 500 ° C. for 2 hours to prepare a Pt catalyst powder supporting 1% by weight of Pt.
一方、 ZrO(NO3)2・2H2Oを104.91ｇと、 Y(NO3)3・6H2Oを8.48ｇとを秤量し、 500ccのイオン交換水中に溶解して混合水溶液を調製した。この混合水溶液に、pHが９になるまでアンモニア水を滴下し、沈殿物を得た。これを実施例１と同様にして濾過・洗浄し、得られた沈殿物を 120℃で12時間乾燥し、さらに 700℃で２時間焼成してZrO2−Y2O3固溶体粉末を調製した。 On the other hand, 104.91 g of ZrO (NO 3 ) 2 · 2H 2 O and 8.48 g of Y (NO 3 ) 3 · 6H 2 O were weighed and dissolved in 500 cc of ion exchange water to prepare a mixed aqueous solution. Ammonia water was added dropwise to the mixed aqueous solution until the pH reached 9, and a precipitate was obtained. This was filtered and washed in the same manner as in Example 1, and the resulting precipitate was dried at 120 ° C. for 12 hours and further calcined at 700 ° C. for 2 hours to prepare a ZrO 2 —Y 2 O 3 solid solution powder.
このZrO2−Y2O3固溶体粉末50ｇを 300ccのイオン交換水に分散し、Rhとして３重量％含有する硝酸ロジウム溶液を8.33ｇ添加して２時間撹拌した。その後 120℃で蒸発・乾固し、 500℃で２時間焼成してRhを 0.5重量％担持したRh触媒粉末を調製した。 50 g of this ZrO 2 —Y 2 O 3 solid solution powder was dispersed in 300 cc of ion-exchanged water, and 8.33 g of a rhodium nitrate solution containing 3% by weight as Rh was added and stirred for 2 hours. Thereafter, it was evaporated and dried at 120 ° C., and calcined at 500 ° C. for 2 hours to prepare Rh catalyst powder carrying 0.5% by weight of Rh.
このようにして得られたPt触媒粉末と、Rh触媒粉末と、γ-Al2O3粉末と、アルミナゾル（固形分10重量％）とを、固形分比でPt触媒粉末：Rh触媒粉末：γ-Al2O3粉末：アルミナゾル＝50：30：７：７の比率で混合し、適量の水を加えてボールミルにて２時間混合して下流側スラリーを調製した。 The Pt catalyst powder, Rh catalyst powder, γ-Al 2 O 3 powder, and alumina sol (solid content: 10% by weight) thus obtained were mixed at a solid content ratio of Pt catalyst powder: Rh catalyst powder: γ. -al 2 O 3 powder: alumina sol = 50: 30: 7: 7 was mixed in a ratio of to prepare a downstream slurry was mixed for 2 hours in a ball mill by adding an appropriate amount of water.
そして酸化触媒部２をもつハニカム基材１の酸化触媒部２を除く37.5mmの部分に下流側スラリーを付着させた後、 250℃で２時間乾燥し、三元触媒部３を形成した。三元触媒部３に形成された触媒層のコート量は5.15ｇであり、ハニカム基材１の１Ｌあたり 147.1ｇである。 A downstream slurry was attached to a 37.5 mm portion excluding the oxidation catalyst portion 2 of the honeycomb substrate 1 having the oxidation catalyst portion 2 and then dried at 250 ° C. for 2 hours to form a three-way catalyst portion 3. The coating amount of the catalyst layer formed on the three-way catalyst portion 3 is 5.15 g, and 147.1 g per liter of the honeycomb substrate 1.
（比較例２）
酸化触媒部２を形成せず、三元触媒部３をハニカム基材１の全長に形成したこと以外は実施例２と同様である。このときの触媒層のコート量は5.13ｇであり、ハニカム基材１の１Ｌあたり 146.6ｇである。
(Comparative Example 2)
Example 3 is the same as Example 2 except that the oxidation catalyst part 2 is not formed and the three-way catalyst part 3 is formed over the entire length of the honeycomb substrate 1. The coating amount of the catalyst layer at this time is 5.13 g, and 146.6 g per liter of the honeycomb substrate 1.
＜試験例２＞
実施例２及び比較例２の触媒をそれぞれ反応管内に配置し、表１に示すリッチガスとリーンガスを１Hzで繰り返しながら30Ｌ／分の流量で流し、25℃／分の速度で室温から ℃まで昇温しながらHC、CO及びNOx の浄化率を連続的に測定した。そしてHC、CO及びNOx をそれぞれ50％浄化できる温度（50％浄化温度）を算出し、結果を初期として図３に示す。
<Test Example 2>
The catalyst of Example 2 and Comparative Example 2 was placed in the reaction tube, and the rich gas and lean gas shown in Table 1 were flowed at a flow rate of 30 L / min while repeating at 1 Hz, and the temperature was raised from room temperature to ℃ at a rate of 25 ℃ / min. The purification rate of HC, CO and NO x was measured continuously. Then, temperatures at which 50% of HC, CO and NO x can be purified (50% purification temperature) are calculated, and the results are shown in FIG. 3 as initial values.
次に表１に示すリッチガスとリーンガスを１分毎に切り替えながら、1000℃で５時間保持する耐久試験を行った。そして耐久試験後のそれぞれの触媒について上記と同様にして50％浄化温度を測定し、結果を耐久後として図３に示す。 Next, an endurance test was performed in which the rich gas and the lean gas shown in Table 1 were maintained at 1000 ° C. for 5 hours while being switched every minute. Then, the 50% purification temperature was measured in the same manner as described above for each catalyst after the durability test, and the result is shown in FIG.
図３から、実施例２の触媒の方が初期及び耐久後の浄化性能に優れていることがわかり、これは酸化触媒部２を形成した効果であることが明らかである。したがって実施例２の触媒を比較例２の触媒と同等の浄化活性とするのであれば、三元触媒部３のコート量を低減することができ、その分安価な触媒とすることができる。 From FIG. 3, it can be seen that the catalyst of Example 2 is superior in purification performance at the initial stage and after the endurance, and it is clear that this is the effect of forming the oxidation catalyst part 2. Therefore, if the catalyst of Example 2 has a purification activity equivalent to that of the catalyst of Comparative Example 2, the coating amount of the three-way catalyst unit 3 can be reduced, and an inexpensive catalyst can be obtained.
（実施例３〜９）
出発原料としてAgNO3、Fe(NO3)3・9H2O、Ce(NO3)3・6H2O、 ZrO(NO3)2・2H2O、Pr(NO3)3・ H2Oから表２に示す組成となるように選択し、実施例１と同様にして触媒粉末をそれ
ぞれ調製した。それぞれの触媒粉末をＸＲＦ及びＸＰＳでそれぞれ分析し、各元素組成を表２に示す。
(Examples 3 to 9)
From AgNO 3 , Fe (NO 3 ) 3 · 9H 2 O, Ce (NO 3 ) 3 · 6H 2 O, ZrO (NO 3 ) 2 · 2H 2 O, Pr (NO 3 ) 3 · H 2 O as starting materials The catalyst powders were prepared in the same manner as in Example 1 by selecting the compositions shown in Table 2. Each catalyst powder was analyzed by XRF and XPS, and each elemental composition is shown in Table 2.
そして実施例２と同様にして、それぞれの触媒粉末からそれぞれスラリーを調製した。次いで実施例２と同様のハニカム基材１を用い、スラリーをそれぞれ全長に付着させた後、 250℃で２時間乾燥し、全長に酸化触媒層を形成して、実施例３〜９の触媒をそれぞれ調製した。酸化触媒層のコート量はそれぞれ約 7.0ｇであり、ハニカム基材１の１Ｌあたり約 200ｇである。 In the same manner as in Example 2, slurries were prepared from the respective catalyst powders. Next, using the same honeycomb substrate 1 as in Example 2, the slurry was adhered to the entire length, and then dried at 250 ° C. for 2 hours to form an oxidation catalyst layer on the entire length, and the catalysts of Examples 3 to 9 were formed. Each was prepared. The coating amount of the oxidation catalyst layer is about 7.0 g, and about 200 g per liter of the honeycomb substrate 1.
（比較例３）
Ce(NO3)3・6H2OとPr(NO3)3・ H2Oとを表２に示す組成で混合し、比較例１と同様にして固溶体粉末を調製した。次にFe(NO3)3・9H2Oの所定量をイオン交換水に溶解し、固溶体粉末に所定量含浸させた後 250℃で２時間乾燥して触媒粉末を調製した。この触媒粉末をＸＲＦ及びＸＰＳで分析し、各元素組成を表２に示す。
(Comparative Example 3)
Ce (NO 3 ) 3 · 6H 2 O and Pr (NO 3 ) 3 · H 2 O were mixed in the composition shown in Table 2, and a solid solution powder was prepared in the same manner as in Comparative Example 1. Next, a predetermined amount of Fe (NO 3 ) 3 · 9H 2 O was dissolved in ion-exchanged water, impregnated with a predetermined amount in a solid solution powder, and then dried at 250 ° C. for 2 hours to prepare a catalyst powder. This catalyst powder was analyzed by XRF and XPS, and each elemental composition is shown in Table 2.
この触媒粉末から、実施例２と同様にしてスラリーを調製した。次いで実施例２と同様のハニカム基材１を用い、スラリーをそれぞれ全長に付着させた後、 250℃で２時間乾燥し、全長に触媒層を形成した。 A slurry was prepared from this catalyst powder in the same manner as in Example 2. Next, the same honeycomb substrate 1 as in Example 2 was used, and each slurry was adhered to the entire length, and then dried at 250 ° C. for 2 hours to form a catalyst layer on the entire length.
（比較例４）
Ce(NO3)3・6H2Oと、 ZrO(NO3)2・2H2Oと、Pr(NO3)3・ H2Oとを表２に示す組成で混合し、比較例１と同様にして固溶体粉末を調製した。次にFe(NO3)3・9H2Oの所定量をイオン交換水に溶解し、固溶体粉末に所定量含浸させた後 250℃で２時間乾燥して触媒粉末を調製した。この触媒粉末をＸＲＦ及びＸＰＳで分析し、各元素組成を表２に示す。
(Comparative Example 4)
Ce (NO 3 ) 3 · 6H 2 O, ZrO (NO 3 ) 2 · 2H 2 O, and Pr (NO 3 ) 3 · H 2 O were mixed in the composition shown in Table 2 and the same as in Comparative Example 1. Thus, a solid solution powder was prepared. Next, a predetermined amount of Fe (NO 3 ) 3 · 9H 2 O was dissolved in ion-exchanged water, impregnated with a predetermined amount in a solid solution powder, and then dried at 250 ° C. for 2 hours to prepare a catalyst powder. This catalyst powder was analyzed by XRF and XPS, and each elemental composition is shown in Table 2.
この触媒粉末から、実施例２と同様にしてスラリーを調製した。次いで実施例２と同様のハニカム基材１を用い、スラリーをそれぞれ全長に付着させた後、 250℃で２時間乾燥し、全長に触媒層を形成した。 A slurry was prepared from this catalyst powder in the same manner as in Example 2. Next, the same honeycomb substrate 1 as in Example 2 was used, and each slurry was adhered to the entire length, and then dried at 250 ° C. for 2 hours to form a catalyst layer on the entire length.
（比較例５）
Ce(NO3)3・6H2Oを用い、比較例１と同様にしてセリア粉末を調製した。次に AgNO3とFe(NO3)3・9H2Oの所定量をイオン交換水に溶解し、セリア粉末に所定量含浸させた後 250℃で２時間乾燥して触媒粉末を調製した。この触媒粉末をＸＲＦ及びＸＰＳで分析し、各元素組成を表２に示す。
(Comparative Example 5)
A ceria powder was prepared in the same manner as Comparative Example 1 using Ce (NO 3 ) 3 .6H 2 O. Next, a predetermined amount of AgNO 3 and Fe (NO 3 ) 3 · 9H 2 O was dissolved in ion exchange water, impregnated with a predetermined amount of ceria powder, and then dried at 250 ° C. for 2 hours to prepare a catalyst powder. This catalyst powder was analyzed by XRF and XPS, and each elemental composition is shown in Table 2.
この触媒粉末から、実施例２と同様にしてスラリーを調製した。次いで実施例２と同様のハニカム基材１を用い、スラリーをそれぞれ全長に付着させた後、 250℃で２時間乾燥し、全長に触媒層を形成した。 A slurry was prepared from this catalyst powder in the same manner as in Example 2. Next, the same honeycomb substrate 1 as in Example 2 was used, and each slurry was adhered to the entire length, and then dried at 250 ° C. for 2 hours to form a catalyst layer on the entire length.
（比較例６）
Ce(NO3)3・6H2Oと、 ZrO(NO3)2・2H2Oとを表２に示す組成で混合し、比較例１と同様にして固溶体粉末を調製した。次に AgNO3の所定量をイオン交換水に溶解し、固溶体粉末に所定量含浸させた後 250℃で２時間乾燥して触媒粉末を調製した。この触媒粉末をＸＲＦ及びＸＰＳで分析し、各元素組成を表２に示す。
(Comparative Example 6)
Ce (NO 3 ) 3 · 6H 2 O and ZrO (NO 3 ) 2 · 2H 2 O were mixed in the composition shown in Table 2, and a solid solution powder was prepared in the same manner as in Comparative Example 1. Next, a predetermined amount of AgNO 3 was dissolved in ion exchange water, impregnated with a predetermined amount in solid solution powder, and then dried at 250 ° C. for 2 hours to prepare a catalyst powder. This catalyst powder was analyzed by XRF and XPS, and each elemental composition is shown in Table 2.
この触媒粉末から、実施例２と同様にしてスラリーを調製した。次いで実施例２と同様のハニカム基材１を用い、スラリーをそれぞれ全長に付着させた後、 250℃で２時間乾燥し、全長に触媒層を形成した。 A slurry was prepared from this catalyst powder in the same manner as in Example 2. Next, the same honeycomb substrate 1 as in Example 2 was used, and each slurry was adhered to the entire length, and then dried at 250 ° C. for 2 hours to form a catalyst layer on the entire length.
（比較例７）
Ce(NO3)3・6H2Oと、 ZrO(NO3)2・2H2Oとを表２に示す組成で混合し、比較例１と同様にして固溶体粉末を調製した。次に AgNO3とFe(NO3)3・9H2Oの所定量をイオン交換水に溶解し、固溶体粉末に所定量含浸させた後 250℃で２時間乾燥して触媒粉末を調製した。この触媒粉末をＸＲＦ及びＸＰＳでそれぞれ分析し、各元素組成を表２に示す。
(Comparative Example 7)
Ce (NO 3 ) 3 · 6H 2 O and ZrO (NO 3 ) 2 · 2H 2 O were mixed in the composition shown in Table 2, and a solid solution powder was prepared in the same manner as in Comparative Example 1. Next, a predetermined amount of AgNO 3 and Fe (NO 3 ) 3 · 9H 2 O was dissolved in ion-exchanged water, impregnated with a predetermined amount in a solid solution powder, and then dried at 250 ° C. for 2 hours to prepare a catalyst powder. The catalyst powder was analyzed by XRF and XPS, and each elemental composition is shown in Table 2.
この触媒粉末から、実施例２と同様にしてスラリーを調製した。次いで実施例２と同様のハニカム基材１を用い、スラリーをそれぞれ全長に付着させた後、 250℃で２時間乾燥し、全長に触媒層を形成した。 A slurry was prepared from this catalyst powder in the same manner as in Example 2. Next, the same honeycomb substrate 1 as in Example 2 was used, and each slurry was adhered to the entire length, and then dried at 250 ° C. for 2 hours to form a catalyst layer on the entire length.
（比較例８）
Ce(NO3)3・6H2Oと、 ZrO(NO3)2・2H2Oとを表２に示す組成で混合し、比較例１と同様にして固溶体粉末を調製した。次に AgNO3とFe(NO3)3・9H2Oの所定量をイオン交換水に溶解し、固溶体粉末に所定量含浸させた後 250℃で２時間乾燥して触媒粉末を調製した。この触媒粉末をＸＲＦ及びＸＰＳでそれぞれ分析し、各元素組成を表２に示す。
(Comparative Example 8)
Ce (NO 3 ) 3 · 6H 2 O and ZrO (NO 3 ) 2 · 2H 2 O were mixed in the composition shown in Table 2, and a solid solution powder was prepared in the same manner as in Comparative Example 1. Next, a predetermined amount of AgNO 3 and Fe (NO 3 ) 3 · 9H 2 O was dissolved in ion-exchanged water, impregnated with a predetermined amount in a solid solution powder, and then dried at 250 ° C. for 2 hours to prepare a catalyst powder. The catalyst powder was analyzed by XRF and XPS, and each elemental composition is shown in Table 2.
この触媒粉末から実施例２と同様にしてスラリーを調製した。次いで実施例２と同様のハニカム基材１を用い、スラリーをそれぞれ全長に付着させた後、 250℃で２時間乾燥し、全長に触媒層を形成した。 A slurry was prepared from this catalyst powder in the same manner as in Example 2. Next, the same honeycomb substrate 1 as in Example 2 was used, and each slurry was adhered to the entire length, and then dried at 250 ° C. for 2 hours to form a catalyst layer on the entire length.
（比較例９）
Ce(NO3)3・6H2Oと、 ZrO(NO3)2・2H2Oと、Pr(NO3)3・ H2Oとを表２に示す組成で混合し、比較例１と同様にして固溶体粉末を調製した。次に AgNO3とFe(NO3)3・9H2Oの所定量をイオン交換水に溶解し、固溶体粉末に所定量含浸させた後 250℃で２時間乾燥して触媒粉末を調製した。この触媒粉末をＸＲＦ及びＸＰＳでそれぞれ分析し、各元素組成を表２に示す。
(Comparative Example 9)
Ce (NO 3 ) 3 · 6H 2 O, ZrO (NO 3 ) 2 · 2H 2 O, and Pr (NO 3 ) 3 · H 2 O were mixed in the composition shown in Table 2 and the same as in Comparative Example 1. Thus, a solid solution powder was prepared. Next, a predetermined amount of AgNO 3 and Fe (NO 3 ) 3 · 9H 2 O was dissolved in ion-exchanged water, impregnated with a predetermined amount in a solid solution powder, and then dried at 250 ° C. for 2 hours to prepare a catalyst powder. The catalyst powder was analyzed by XRF and XPS, and each elemental composition is shown in Table 2.
この触媒粉末から、実施例２と同様にしてスラリーを調製した。次いで実施例２と同様のハニカム基材１を用い、スラリーをそれぞれ全長に付着させた後、 250℃で２時間乾燥し、全長に触媒層を形成した。 A slurry was prepared from this catalyst powder in the same manner as in Example 2. Next, the same honeycomb substrate 1 as in Example 2 was used, and each slurry was adhered to the entire length, and then dried at 250 ° C. for 2 hours to form a catalyst layer on the entire length.
＜試験例３＞ <Test Example 3>
各実施例及び各比較例の触媒を反応管にそれぞれ配置し、試験例１と同様にして 500℃における浄化率を測定するとともに、試験例２と同様にして初期及び耐久後の50％浄化温度を測定した。結果を表３に示す。 The catalyst of each Example and each Comparative Example was placed in a reaction tube, and the purification rate at 500 ° C. was measured in the same manner as in Test Example 1, and the 50% purification temperature after the initial and endurance was the same as in Test Example 2. Was measured. The results are shown in Table 3.
１：ハニカム基材 ２：酸化触媒部 ３：三元触媒部 1: Honeycomb base material 2: Oxidation catalyst part 3: Three-way catalyst part
Claims (5)
The exhaust gas purifying catalyst according to any one of claims 1 to 4, wherein the composite oxide is disposed on the exhaust gas upstream side of the three-way catalyst.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2004128626A JP4547607B2 (en) | 2004-04-23 | 2004-04-23 | Exhaust gas purification catalyst |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2004128626A JP4547607B2 (en) | 2004-04-23 | 2004-04-23 | Exhaust gas purification catalyst |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005305363A true JP2005305363A (en) | 2005-11-04 |
| JP4547607B2 JP4547607B2 (en) | 2010-09-22 |
Family
ID=35434737
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004128626A Expired - Fee Related JP4547607B2 (en) | 2004-04-23 | 2004-04-23 | Exhaust gas purification catalyst |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP4547607B2 (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010094629A (en) * | 2008-10-17 | 2010-04-30 | Mazda Motor Corp | Catalyst for cleaning exhaust gas |
| WO2014006335A1 (en) * | 2012-07-04 | 2014-01-09 | Commissariat A L'energie Atomique Et Aux Energies Alternatives | Catalytic method for the production of carbon monoxide and associated reactor |
| FR2992872A1 (en) * | 2012-07-04 | 2014-01-10 | Commissariat Energie Atomique | New catalyst useful in the production of synthesis gas used to synthesize hydrocarbon such as methanol, dimethyl ether or paraffin, comprises comprising iron, silver and cerium |
| US9962684B2 (en) | 2014-03-25 | 2018-05-08 | Daiichi Kigenso Kagaku Kogyo Co., Ltd. | Cerium-zirconium-based composite oxide and method for producing same |
Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01281144A (en) * | 1988-04-30 | 1989-11-13 | Toyota Central Res & Dev Lab Inc | Catalyst for purifying exhaust gas |
| JPH0549943A (en) * | 1991-08-20 | 1993-03-02 | Sakai Chem Ind Co Ltd | Oxidizing catalyst |
| JPH06315634A (en) * | 1992-12-14 | 1994-11-15 | Sekiyu Sangyo Kasseika Center | Catalytic structure for nitrogen oxide catalytic reduction |
| JPH07155601A (en) * | 1993-10-14 | 1995-06-20 | Toyota Motor Corp | Exhaust gas purifying catalyst |
| JPH0824648A (en) * | 1994-07-22 | 1996-01-30 | Nissan Motor Co Ltd | Exhaust gas purifying catalyst and preparation of the sam |
| JPH11207190A (en) * | 1998-01-27 | 1999-08-03 | Mazda Motor Corp | Catalyst for purification of exhaust gas and its production |
| JP2000510761A (en) * | 1996-05-14 | 2000-08-22 | エンゲルハード・コーポレーシヨン | Exhaust gas catalyst including a multilayer zone upstream |
| JP2001241321A (en) * | 2000-02-29 | 2001-09-07 | Nissan Motor Co Ltd | Exhaust gas emission control device for internal combustion engine and exhaust gas emission control method |
| JP2004008977A (en) * | 2002-06-07 | 2004-01-15 | Valtion Teknillinen Tutkimuskeskus | Method for catalytically removing nitrogen oxide and apparatus therefor |
-
2004
- 2004-04-23 JP JP2004128626A patent/JP4547607B2/en not_active Expired - Fee Related
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01281144A (en) * | 1988-04-30 | 1989-11-13 | Toyota Central Res & Dev Lab Inc | Catalyst for purifying exhaust gas |
| JPH0549943A (en) * | 1991-08-20 | 1993-03-02 | Sakai Chem Ind Co Ltd | Oxidizing catalyst |
| JPH06315634A (en) * | 1992-12-14 | 1994-11-15 | Sekiyu Sangyo Kasseika Center | Catalytic structure for nitrogen oxide catalytic reduction |
| JPH07155601A (en) * | 1993-10-14 | 1995-06-20 | Toyota Motor Corp | Exhaust gas purifying catalyst |
| JPH0824648A (en) * | 1994-07-22 | 1996-01-30 | Nissan Motor Co Ltd | Exhaust gas purifying catalyst and preparation of the sam |
| JP2000510761A (en) * | 1996-05-14 | 2000-08-22 | エンゲルハード・コーポレーシヨン | Exhaust gas catalyst including a multilayer zone upstream |
| JPH11207190A (en) * | 1998-01-27 | 1999-08-03 | Mazda Motor Corp | Catalyst for purification of exhaust gas and its production |
| JP2001241321A (en) * | 2000-02-29 | 2001-09-07 | Nissan Motor Co Ltd | Exhaust gas emission control device for internal combustion engine and exhaust gas emission control method |
| JP2004008977A (en) * | 2002-06-07 | 2004-01-15 | Valtion Teknillinen Tutkimuskeskus | Method for catalytically removing nitrogen oxide and apparatus therefor |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010094629A (en) * | 2008-10-17 | 2010-04-30 | Mazda Motor Corp | Catalyst for cleaning exhaust gas |
| WO2014006335A1 (en) * | 2012-07-04 | 2014-01-09 | Commissariat A L'energie Atomique Et Aux Energies Alternatives | Catalytic method for the production of carbon monoxide and associated reactor |
| FR2992872A1 (en) * | 2012-07-04 | 2014-01-10 | Commissariat Energie Atomique | New catalyst useful in the production of synthesis gas used to synthesize hydrocarbon such as methanol, dimethyl ether or paraffin, comprises comprising iron, silver and cerium |
| FR2992954A1 (en) * | 2012-07-04 | 2014-01-10 | Commissariat Energie Atomique | CATALYTIC PROCESS FOR PRODUCING CARBON MONOXIDE AND REACTOR THEREOF |
| US9962684B2 (en) | 2014-03-25 | 2018-05-08 | Daiichi Kigenso Kagaku Kogyo Co., Ltd. | Cerium-zirconium-based composite oxide and method for producing same |
Also Published As
| Publication number | Publication date |
|---|---|
| JP4547607B2 (en) | 2010-09-22 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US8853120B2 (en) | Double layered exhaust gas purification catalyst | |
| CN1134297C (en) | Catalyst composition containing oxygen storage components | |
| JP5910833B2 (en) | Exhaust gas purification catalyst | |
| JP6007248B2 (en) | Exhaust gas purification catalyst composition and automobile exhaust gas purification catalyst | |
| JPH09141098A (en) | Catalyst for purification of exhaust gas and its production | |
| JPWO2006030763A1 (en) | Cerium-zirconium composite oxide, method for producing the same, oxygen storage / release material using the same, exhaust gas purification catalyst, and exhaust gas purification method | |
| JP6869976B2 (en) | Three-way catalyst for purifying gasoline engine exhaust gas | |
| EP3616789A1 (en) | Exhaust gas purification catalyst and exhaust gas purification method using same | |
| JP4831753B2 (en) | Exhaust gas purification catalyst | |
| JP3216858B2 (en) | Exhaust gas purification catalyst and method for producing the same | |
| US11141713B2 (en) | Exhaust gas purification catalyst and exhaust gas purification method using the same | |
| JP2007289921A (en) | Exhaust-gas cleaning catalyst and its regeneration method | |
| JP2009000648A (en) | Exhaust gas cleaning catalyst | |
| JP2006205002A (en) | Catalyst for cleaning exhaust gas | |
| JP5531567B2 (en) | Exhaust gas purification catalyst | |
| JP4547607B2 (en) | Exhaust gas purification catalyst | |
| JP5806157B2 (en) | Exhaust gas purification catalyst composition | |
| JP2006035043A (en) | Catalyst for purifying exhaust gas | |
| JP2002282692A (en) | Catalyst for cleaning exhaust gas | |
| JPH10277389A (en) | Catalyst for cleaning exhaust gas | |
| JP4830293B2 (en) | Composite oxide, method for producing the same, and catalyst for purification of exhaust gas | |
| EP3616790A1 (en) | Exhaust gas purification catalyst and exhaust gas purification method using same | |
| JP3309711B2 (en) | Exhaust gas purification catalyst and method for producing the same | |
| JP4265445B2 (en) | Exhaust gas purification catalyst | |
| JPH0857312A (en) | Highly heat resistant catalyst for purification of exhaust gas |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20070108 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20090403 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20090804 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20091001 |
|
| TRDD | Decision of grant or rejection written | ||
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20100610 |
|
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20100623 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20130716 Year of fee payment: 3 |
|
| LAPS | Cancellation because of no payment of annual fees |