WO2006109849A1 - 窒素酸化物を接触還元するための触媒、触媒構造体及び窒素酸化物を接触還元するための方法 - Google Patents
窒素酸化物を接触還元するための触媒、触媒構造体及び窒素酸化物を接触還元するための方法 Download PDFInfo
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- WO2006109849A1 WO2006109849A1 PCT/JP2006/307800 JP2006307800W WO2006109849A1 WO 2006109849 A1 WO2006109849 A1 WO 2006109849A1 JP 2006307800 W JP2006307800 W JP 2006307800W WO 2006109849 A1 WO2006109849 A1 WO 2006109849A1
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- Prior art keywords
- catalyst
- catalyst component
- oxide
- exhaust gas
- oxides
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- 238000000034 method Methods 0.000 title claims abstract description 44
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims abstract description 95
- 239000007789 gas Substances 0.000 claims abstract description 63
- CETPSERCERDGAM-UHFFFAOYSA-N ceric oxide Chemical compound O=[Ce]=O CETPSERCERDGAM-UHFFFAOYSA-N 0.000 claims abstract description 44
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- MVFCKEFYUDZOCX-UHFFFAOYSA-N iron(2+);dinitrate Chemical compound [Fe+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O MVFCKEFYUDZOCX-UHFFFAOYSA-N 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 150000002603 lanthanum Chemical class 0.000 description 1
- FYDKNKUEBJQCCN-UHFFFAOYSA-N lanthanum(3+);trinitrate Chemical compound [La+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O FYDKNKUEBJQCCN-UHFFFAOYSA-N 0.000 description 1
- 238000002796 luminescence method Methods 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- CFYGEIAZMVFFDE-UHFFFAOYSA-N neodymium(3+);trinitrate Chemical compound [Nd+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O CFYGEIAZMVFFDE-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 1
- GPNDARIEYHPYAY-UHFFFAOYSA-N palladium(ii) nitrate Chemical compound [Pd+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O GPNDARIEYHPYAY-UHFFFAOYSA-N 0.000 description 1
- 235000011197 perejil Nutrition 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 229910052705 radium Inorganic materials 0.000 description 1
- HCWPIIXVSYCSAN-UHFFFAOYSA-N radium atom Chemical compound [Ra] HCWPIIXVSYCSAN-UHFFFAOYSA-N 0.000 description 1
- 238000010405 reoxidation reaction Methods 0.000 description 1
- YZDZYSPAJSPJQJ-UHFFFAOYSA-N samarium(3+);trinitrate Chemical compound [Sm+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O YZDZYSPAJSPJQJ-UHFFFAOYSA-N 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 229910021332 silicide Inorganic materials 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229910001923 silver oxide Inorganic materials 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000011949 solid catalyst Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000011232 storage material Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- YJVUGDIORBKPLC-UHFFFAOYSA-N terbium(3+);trinitrate Chemical compound [Tb+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O YJVUGDIORBKPLC-UHFFFAOYSA-N 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 239000010938 white gold Substances 0.000 description 1
- 229910000832 white gold Inorganic materials 0.000 description 1
Classifications
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- B01D53/34—Chemical or biological purification of waste gases
- B01D53/92—Chemical or biological purification of waste gases of engine exhaust gases
- B01D53/94—Chemical or biological purification of waste gases of engine exhaust gases by catalytic processes
- B01D53/9404—Removing only nitrogen compounds
- B01D53/9409—Nitrogen oxides
- B01D53/9413—Processes characterised by a specific catalyst
- B01D53/9422—Processes characterised by a specific catalyst for removing nitrogen oxides by NOx storage or reduction by cyclic switching between lean and rich exhaust gases (LNT, NSC, NSR)
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- B01J23/8933—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with noble metals also combined with metals, or metal oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
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- B01J29/18—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the mordenite type
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- B01J29/70—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of types characterised by their specific structure not provided for in groups B01J29/08 - B01J29/65
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- B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
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- B01J29/70—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of types characterised by their specific structure not provided for in groups B01J29/08 - B01J29/65
- B01J29/72—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of types characterised by their specific structure not provided for in groups B01J29/08 - B01J29/65 containing iron group metals, noble metals or copper
- B01J29/76—Iron group metals or copper
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- B01J35/00—Catalysts, in general, characterised by their form or physical properties
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- B01J35/61—Surface area
- B01J35/615—100-500 m2/g
Definitions
- the present invention Catalytic reduction by contact with nitrogen oxides (mainly composed of NO and N 0 2 , hereinafter referred to as NOx), that is, a catalyst for catalytic reduction, and such a catalyst And a method for catalytic reduction of nitrogen oxides in exhaust gas.
- NOx nitrogen oxides
- the present invention provides a diesel engine or gasoline engine 10 in a periodic rich / lean fuel supply stroke (excursion) to supply fuel to the gin combustion chamber for combustion, and the generated exhaust gas contacts the catalyst. It is related to a catalyst and such a method for catalytic reduction of 'N Ox in exhaust gas.
- Such a catalyst and a method using the same according to the present invention are suitable for reducing and removing harmful nitrogen oxides contained in, for example, exhaust gas from automobile engines.
- the present invention provides fuel in a periodic rich / lean fuel supply process in the presence of sulfur oxides (mainly composed of S 0 2 and S 0 3 , hereinafter referred to as S 0x). Relating to a catalyst and a method for catalytically reducing NOx in exhaust gas produced by the combustion without deterioration of the catalyst. '' + ' ⁇
- stroke J (excursion) means that the air / fuel ratio is AJ in both directions from the average value along the time axis. X means such work. "'Leach J becomes.
- Zu means a catalyst or structure containing it that operates to leave 0 during combustion.
- Nx contained in exhaust gas is, for example, oxidized and then absorbed into alkali, or reduced to nitrogen using ammonia, hydrogen, carbon monoxide or hydrocarbon as a reducing agent, etc. Has been removed by the method.
- each of these conventional methods has drawbacks.
- a means for treating the generated alkaline wastewater is necessary to prevent environmental problems.
- ammonia when used as a reducing agent, ammonia reacts with SOx in the exhaust gas to form salts, and as a result, the catalytic activity is reduced at low temperatures.
- the safety of NO x from mobile sources such as automobiles is a problem.
- the reducing agent will react preferentially with the oxygen because the exhaust gas contains oxygen at a higher concentration than Nx.
- N Ox is to be substantially reduced, a large amount of reducing agent is required, resulting in a significant reduction in fuel consumption.
- the system has a problem that the system deteriorates rapidly due to mechanical absorption.
- a surface catalyst layer having, as a surface catalyst component, at least one selected from a complex oxide of two elements;
- a catalyst comprising an internal catalyst layer having as an internal catalyst component is close to the NOx storage-reduction system and exhibits NOx purification ability and high SOx durability.
- a first catalyst component selected from rhodium, palladium and oxides thereof, zirconia, cerium oxide, praseodymium oxide
- Catalysts have been proposed as exhibiting high S Ox durability. Disclosure of the invention
- fuel is burned under periodic rich / lean conditions in the presence of oxygen, sulfur oxides or water, and over a wide range of reaction temperatures
- a catalyst capable of catalytic reduction of NOx in a high durability without deterioration of the catalyst, and a method for catalytic reduction of nitrogen oxides in exhaust gas using such a catalyst.
- the present invention is particularly effective in the presence of oxygen, sulfur oxides or water, especially in the presence of sulfur oxides, which are serious problems of NOx storage catalysts.
- Another object of the present invention is to provide a catalyst structure for NOx contact reduction in which the above-mentioned catalyst is supported on an inert support substrate.
- a catalyst for supplying and burning fuel under periodic rich / lean conditions contacting the generated exhaust gas, and catalytically reducing nitrogen oxides in the exhaust gas.
- A (a) Solid acid and.
- noble metal catalyst component B consisting of at least one selected from platinum, rhodium, and 'palladium R and their oxides' and
- ID (d) Praseodymium oxide or.
- a catalyst for catalytic reduction of nitrogen oxides in exhaust gas comprising an internal catalyst layer having 15 as an internal catalyst component.
- the catalyst structure is formed by adding the above-mentioned solvent to a base material that is active. . ::
- a method for supplying and burning fuel under periodic ritino-lean conditions bringing the produced exhaust gas into contact with a catalyst, and catalytically reducing nitrogen oxides in the exhaust gas.
- the catalyst is'.
- a noble metal catalyst component B consisting of at least one selected from platinum, rhodium, palladium and oxides thereof;
- the internal catalyst component is obtained by supporting the catalyst component B on the catalyst component C.
- the internal catalyst component is obtained by supporting the catalyst component B on the catalyst component C and a conventionally known carrier such as alumina.
- FIG. 1 shows the time of the concentration of nitrogen in a gas when a gas containing nitrogen oxide is treated at a reaction temperature of 2500 to 400 ° C using an example of the catalyst according to the present invention ( Changes due to rich Z-lean time).
- Fig. 2 shows the time of the concentration of nitrogen in a gas when a gas containing nitrogen oxide was treated over a reaction temperature of 2500 to 400 ° C using an example of a catalyst according to a comparative example ( (Litch Z-lean time).
- the catalytic reduction of nitrogen oxides means that NOx adsorbed on the catalyst at the time of lean is converted into ammonia by a catalytic reaction at the time of rich, and this ammonia is accumulated on the solid acid of the catalyst, and thus Accumulated ammonia reacts with NOx in the presence of oxygen when lean, and NOx is converted to nitrogen and water, carbon monoxide, carbon dioxide, etc. with high efficiency throughout the entire rich process.
- the NOx storage-reduction system described in the above-mentioned WO 93 / 7.363 and WO 93/8383 has the following characteristics. As shown in Fig. 2.
- the catalyst for catalytic reduction of nitrogen oxides in #gas is produced by supplying fuel under periodic rich / lean conditions and bringing it into contact with the generated exhaust gas.
- Nitrogen in exhaust gas '...' is a catalyst for catalytic reduction of elemental oxides. This catalyst is ...
- the catalyst component C is sometimes referred to as an oxygen storage material in some cases, paying attention to the fact that it has an oxygen storage function.
- the catalyst according to the present invention is preferably a two-layer catalyst having a surface catalyst layer and an internal catalyst layer, wherein the surface catalyst layer is exposed so as to be in direct contact with the exhaust gas.
- the catalyst according to the present invention is used as a catalyst structure having a surface catalyst layer and an internal catalyst layer in this order on an inert substrate made of clay or metal.
- the catalyst component C has, as one aspect, at least two element acids and / or complex acids (solid solution), as described as component (e), ie,
- the mixture may be at least one selected from a mixture of at least two elements and at least a composite oxide (solid solution) of the two elements, but the mixture is preferably a uniform mixture.
- the composite oxide of the at least two elements is preferably used rather than the mixture of the oxides of the at least two elements.
- the binary or ternary composite oxidation is used.
- the product is preferably used.
- the weight ratio of each element in the solid solution is determined as follows: praseodymium complex oxide, cerianozirconia complex oxide, terbium oxide terbium complex oxide
- praseodymium complex oxide cerianozirconia complex oxide
- terbium oxide terbium complex oxide In the case of an oxide, a seria / samarium oxide composite oxide, etc., it is preferably in the range of 80 Z 2 0 to 60 0/40.
- the oxide-based weight ratio in the solid solution is ceria / gadolinium oxide / zirconia composite oxide, ceria / neodymium oxide Z-zirconia composite oxide, ceria / zirconia hydrated praseodymium composite oxide.
- Ceria / zirconia / lanthanum oxide composite oxide, ceria / zirconia / samarium oxide composite oxide, ceria Z zirconia Z acid terbium complex oxide, etc. preferably from 4 5/30 Z 30 It is in the range of 7 5/2 0/5.
- the oxide-based weight ratio of each element in these composite silicides is ceria, zirconia, terbium oxide, praseum oxide, gadolinium oxide, neodymium oxide, samarium oxide, and lanthanum oxide.
- the catalyst component C. in the catalyst according to the present invention can be prepared, for example, by the following method. That is, first, a water-soluble salt of an element constituting a catalyst component, for example, an aqueous solution of nitrate; 5 ′ ′-neutralized or subjected to hydrolysis by heating to form a hydroxide.
- the product may be calcined at a temperature of 300 to 900 ° C. in an oxidizing or ':' atmosphere.
- the catalyst component C can also be obtained by commercially calcining a hydroxide or oxide of the above-mentioned element as described above.
- the solid acid of the catalyst component ⁇ may be selected from acids such as H—Y zeolite, H—suldenite, 10 H—) 3 zeolite, H—ZSM, 5, and H—SUZ—4. Oxidation. Titanium, zirconia, silica-alumina, etc. can be used. Of these, H-mordenite is most preferably used from the viewpoint of ammonia adsorption.
- the solid acid carrying the metal oxide is a solid acid such as the oxide or Z or ion of at least one element selected from vanadium, tungsten, ribden, copper, iron, cobalt, nickel and manganese. Is a catalyst component supported on the catalyst.
- the oxide to be supported on the solid acid must be selected according to the reaction temperature when treating the exhaust gas, but in the region where the reaction temperature is 20 to 300 ° C, vanadium or copper Oxides are preferably used. On the other hand, in the region where the reaction temperature is 300 ° C. or higher, oxides of tungsten, molybdenum, iron, cobalt, nickel or manganese are often used.
- the oxide component and / X is a catalyst component composed of an ion-supported solid acid. It can be prepared by an oxide loading method, for example, an impregnation method, an ion exchange method, a kneading method, etc. + '' ⁇ '.
- ⁇ ⁇ ⁇ ⁇ ⁇ According to the present invention : ⁇ ⁇ ⁇ ⁇ :: ⁇ ⁇ ⁇ and solid acids carrying ⁇ ⁇ or ions
- the catalyst according to this book is a two-layer catalyst with a surface catalyst layer and a 3 ⁇ 4 part catalyst layer. Therefore, the surface catalyst component of the surface catalyst layer is composed of the catalyst component A, and the internal catalyst component of the internal catalyst layer is composed of a combination of the catalyst components B and C.
- the weight ratio of the surface catalyst component / internal catalyst component is preferably in the range of 1 to 10. In the present invention, this weight ratio greatly affects the NOx reduction ability in the rich / lean process of the catalyst.
- the preferred value of this weight ratio depends on the reaction conditions such as temperature, oxygen concentration, space velocity (SV), etc.
- the preferred weight ratio at which high NOx reduction ability can be obtained in the rich / lean process is In the range of 3 to 7.5. However, usually around 5 is preferred. Even if the weight ratio is 1 or less, the performance does not improve commensurately, and the diffusion of NOx and the reducing agent into the internal catalyst layer is hindered. Also, when the weight ratio is greater than 10, the NOx adsorption rate during lean decreases, the ammonia production rate decreases during rich, and the selective reduction reaction of NOx by ammonia during lean becomes insufficient. As a result, the NOx purification capacity decreases.
- the internal catalyst component of the internal catalyst layer is composed of the catalyst components B and C.
- the catalyst component B that is, the noble metal catalyst component
- the catalyst component C is supported on the catalyst component C.
- the catalyst component C and the support are supported.
- the carrier conventionally known ones such as alumina, silica, silica monoalumina, zeolite, titania and the like are appropriately used.
- the noble metal catalyst component B is preferably in the range of 0.5 to 5% by weight in the internal catalyst component, while the carrier is 5 to 5% in the internal catalyst component. It is used in the range of 50% by weight.
- the catalyst component C since the catalyst component C has an OSC function, when this OSC function is strong, a response delay occurs when the gas atmosphere is changed from lean to rich, and as a result, ammonia is generated. The rate drops. Therefore, by replacing a part of the catalyst component C carrying the metal catalyst component B in the internal catalyst layer with a carrier having no OSC function, it is possible to prevent the response delay from occurring.
- the two-layer catalyst having the surface catalyst layer and the inner catalyst layer as described above has a catalyst structure in which the inner catalyst layer and the surface catalyst layer are laminated in this order on an inert base material. Used as a body.
- the ratio of the noble metal catalyst component B in the inner catalyst layer is Minutes are in the range of 0.5 to 5% by weight in terms of metal. 'Even if the ratio of the precious metal catalyst component ⁇ in the internal catalyst component exceeds 5.% by weight in terms of metal, the ammonia production rate in the rich state does not improve. The oxidation of ammonia adsorbed on the surface is promoted, and the selectivity of the selective reduction reaction between N0x and ammonia at the time of rinsing is lowered. On the other hand, when the proportion of the “5- + noble metal catalyst component in the internal catalyst component is less than 0.5% by weight in terms of the parent metal, the formation of ammonia by the reducing agent is reduced.
- the ion exchange of the carrier has a limit. The ions and oxides are often held in a mixed state.
- the internal catalyst component is preferably, for example, first supported by a suitable means such as impregnation method or ion exchange method on a support such as catalyst component C or alumina. And then calcining in an oxidizing or reducing atmosphere at a temperature of 500 to 90 ° C to obtain a powder in which the noble metal catalyst component is supported on the catalyst component C or the support.
- a catalyst component C loaded with a noble metal catalyst component and a carrier such as alumina loaded with a noble metal catalyst component can be prepared and mixed.
- Catalyst component ⁇ has twin how NO adsorption sites and N_ ⁇ 2 adsorption sites. Depending on the type of oxide used, in general, it is greater N0 2 adsorption site amount. In this way, the catalyst component B containing the noble metal catalyst is responsible for reducing the NOx adsorbed on the catalyst component A. In the lean period, 25 .. Converts cocoons and '.'N Ox: functions to increase adsorption rate.
- the medium component can be obtained in various forms such as a powder or a granular material.
- a honeycomb an annular material, a spherical material, and the like by using any of the catalyst components by any well-known method.
- an appropriate additive such as a molding aid, a reinforcing material, an inorganic fiber, an organic binder, or the like can be used as necessary.
- the catalyst according to the present invention provides a catalyst structure having a catalyst layer on the surface of an inert base material for support having an arbitrary shape, for example, by a wash coat method (for example, by coating).
- the inert base material is, for example, a clay mineral such as cordierite, a metal such as stainless steel, and preferably a heat-resistant metal such as Fe-Cr-A1.
- the shape may be a honeycomb, an annular shape, a spherical structure, or the like.
- the catalyst components for the surface catalyst layer and the internal catalyst layer can be obtained in various forms such as powder and granular materials.
- the internal catalyst layer is formed into various shapes such as a honeycomb, an annular material, a spherical material, and the like by using any of the internal catalyst components by a well-known method.
- a surface catalyst component and forming a surface catalyst layer on the surface of the internal catalyst layer catalyst structures of various shapes can be obtained.
- an appropriate additive such as a molding aid, a reinforcing material, an inorganic fiber, an organic binder, or the like can be used as necessary.
- All of the catalysts according to the present invention not only have excellent resistance to heat, but also excellent resistance to sulfur oxides. Reduction of N0x in diesel engine and lean gasoline engine automobile exhaust gas, that is, It is suitable for use as a catalyst for denitration.
- the catalyst according to the present invention is preferably used in a catalytic reaction under conditions where the combustion atmosphere of the fuel oscillates between rich conditions and lean conditions as described above.
- the period of the catalytic reaction (that is, the time from the rich atmosphere (or lean atmosphere) to the next rich atmosphere (or lean atmosphere)) is preferably 5 to 150 seconds, particularly preferably 3 0 ⁇ 90 seconds.
- the rich time is preferably in the range of 0.1 to 10 seconds
- the lean time is preferably in the range of 5 to 150 seconds
- the rich / The ratio of lean width is usually in the range of 0.2 to 0.1.
- the rich condition is usually formed by periodically injecting fuel into the combustion chamber of the engine at an air / fuel ratio of 10 'to 14 by weight when using gasoline as the fuel.
- Re Typical exhaust gas under several tactile conditions is several hundred volumes Ppm Nx, 5-6 vol% water, '2 3 vol% carbon monoxide, 2-3 vol% hydrogen, several thousand capacities Contains ppm hydrocarbons and 0-0.5 vol% oxygen.
- the lean condition is that when gasoline is used as fuel, fuel is usually injected periodically into the engine combustion chamber at an air / fuel ratio of 20 to 40 by weight. 5 'forming.
- the preferred temperature for NOx catalytic reduction using the catalyst according to the present invention depends on the individual gas composition, but has a catalytic reaction activity that is effective against NOx over a long period of time in the rich stroke. Usually, it is in the range of .5 Q to .5.5.0 ', Preferred: Guho, in the range of 2 0 0 to 5.0 0 ° G.
- the exhaust gas is preferably treated at a space velocity in the range of .5 0 0 0 to 1 5 0.0 0 0 ′ h ⁇ 1 .
- NOx-containing exhaust gas is contacted with the above-described catalyst in a periodic rich / lean process. '', Even in the presence of oxygen, yellow oxide or moisture 15. Nx in exhaust gas can be catalytically reduced stably and efficiently. Industrial applicability.
- ⁇ '' ⁇ ⁇ : with manufacturing examples of the powder catalyst is a catalyst component below, 'which ⁇ Ru honeycomb: Made in the catalyst structure
- cerium nitrate (Ce ( ⁇ 0 3 ) 3 ⁇ 6H 2 ⁇ ) 151.37 g to 100 OmL of ion-exchanged water to make an aqueous solution, and add 0.1 N ammonia water to this to neutralize cerium ions. Decomposed and aged for 1 hour. The obtained slurry was filtered, dried at 120 ° C. for 24 hours, and then calcined in air at 500 ° C. for 3 hours to obtain ceria powder (specific surface area 138 m 2 Zg). Production example 2.
- cerium nitrate (C e ( ⁇ 0 3 ) 3 ⁇ 6H 2 0) 164.31 and praseodymium nitrate ( ⁇ ⁇ ( ⁇ 0 3 ) 3 ⁇ 6 ⁇ 2 0) 4. 4 7 g in 100 OmL of ion-exchanged water An aqueous solution was prepared. 0.1N aqueous ammonia was added to this aqueous solution to neutralize and hydrolyze the cerium salt and praseodymium salt, and then aged for 1 hour.
- Ion-exchanged water 100 OmL to cerium nitrate (C e ( ⁇ 0 3 ) 3 ⁇ 6H 2 0) 164.31 g and praseodymium nitrate (P r ( ⁇ 0 3 ) 3 ⁇ 6H 2 0) 2. 24 g and lanthanum nitrate ( L a (N0 3) 3 - 6H 2 0) 3. by dissolving the 98 g, to prepare an aqueous solution. 0.1N ammonia water was added to this aqueous solution, and the above sericum salt, praseodymium salt and lanthanum salt were neutralized and hydrolyzed and then aged for 1 hour.
- Ion-exchanged water 1 00 OmL with cerium nitrate (C e ( ⁇ 0 3 ) 3 ⁇ 6H 2 0) 1 09.43 g and zirconium oxynitrate (Z rO (N0 3 ) 2 ) 3 1.27 g and neodymium nitrate (Nd (N0 3 ) 3- • ⁇ 6H 2 0) 1 5. 63 g was dissolved to prepare an aqueous solution. 0.1 N ammonia water was added to this aqueous solution to neutralize and hydrolyze the above-mentioned cerium salt, oxyzirconium salt and neodymium salt, and then aged for 1 hour.
- the resulting product is separated from the resulting slurry by filtration, dried at 120 for 24 hours, and then calcined in air at 500 ° C for 3 hours to form a ceria / zirconia Z-acid neodymium composite oxide.
- a powder (weight ratio based on oxide 70 0 20 Z 1.0, specific surface area 17 1 m 2 / g) was obtained. -. '' ⁇ ⁇
- Ion-exchanged water 100 OmL with cerium nitrate (Ce (N0 3 ) 3 ⁇ 6H 2 0) 121. 06 and zirconium oxynitrate (ZrO (N0 3 ) 2 ) 28.12 g and samarium nitrate (Sm (N0 3 ) 3 ⁇ 6H 2 0) 3. 40 g was dissolved to prepare an aqueous solution. 0.1N ammonia water was added to this aqueous solution to neutralize and hydrolyze the above-mentioned cerium salt, oxyzirconium salt and samarium salt, and then aged for 1 hour.
- Production example 1 Production Example 8, in place of the Seria powder prepared in Production Example 1, Production Example 2: - obtained Seria Z praseodymium oxide composite oxide powder (oxide basis weight ratio 95/5 and a specific surface area 1 82m z In the same manner as above, a catalyst powder in which 2% white gold was supported on a silica / praseodymium oxide composite oxide was obtained. ..: ', Five - '
- Example 8 instead of the ceria powder prepared in Production Example 1, ⁇ In Production Example 4, the obtained cerianozirconia / gadolinium oxide composite oxide powder (weight ratio based on oxide 72 Z 2 15 4 / 4, except that a specific surface area of 198 m 2 / g was used, in the same manner, a catalyst powder having 2% platinum supported on a ceria / zircoair / acid gadolinium composite oxide was obtained.
- Example 14 +. ':.'
- Example 8 Oite, Preparation'.. Instead of preparing accident rear powders in Example 1, 'Preparation 6 placed obtained ceria / Sani ⁇ terbium complex oxide powder ( Ceria oxide terbium complex compound Ji ko platinum, except that oxide capping fi ratio 7.0 Z.30, specific surface area 1, .. ' ⁇ ' .. 39 m 2 Zg) was used. % A catalyst housing supported was obtained. .. Production Example 16
- the above-mentioned 25 Washing coating slurry is applied.
- U ': H is also a contact component composed of lute * nitrate.
- Example 4 a catalyst component obtained by supporting 2% platinum and 0.5% palladium on the ceria obtained in Production Example 10 was used as an internal catalyst layer at a rate of 150 g / L (honeycomb volume). And having a catalyst component made of titanium oxide carrying V 2 0 5 1% and W 0 3 10% obtained in Production Example 20 as a surface catalyst layer at a rate of 50 g / L (honeycomb volume). A catalyst structure was obtained.
- Example 4
- Silica sol 12 g and an appropriate amount of water were mixed with 60 g of the catalyst powder obtained by supporting 2% platinum on the alumina alumina ceria (weight ratio 1Z1) obtained in Production Example 16. Using 100 g of zirconia as a dusting medium, this mixture was ground with a planetary mill for 5 minutes to obtain a wash coat slurry. Honeycomb having the above catalyst coated on the cordierite eighty-cam base with 400 cells per square inch and having the above catalyst as an internal catalyst layer at a rate of 150 g / L (volume of Nicum) A structure was obtained.
- Example 6 In the same manner as in Example 4, the ratio of the catalyst obtained by supporting 2% platinum on the monoaluminose ceria (weight ratio 1/5) obtained in Production Example 17 was 150 g / L and the volume of the two cams) As an internal catalyst layer ”and with Cu01% supported—a zeolite catalyst consisting of 50 g / A honeycomb catalyst structure having a surface layer catalyst layer at a ratio of (2 cam volume) + was obtained.
- the catalyst obtained by supporting white / 5 ′ ′ gold 2.% on the ceria / praseodymium oxide composite oxide obtained in Production Example 11 is 15 O′g / L, and the two-cam volume. ))
- a honeycomb catalyst structure having a surface catalyst layer in a proportion was obtained.
- Example 10 In the same manner as in Example 4, the ceria Z-acid praseodymium Z-oxide run obtained in Production Example 12 was used.
- Example 10 Selenium / zirconia / neodymium oxide 'complex acid obtained in 1: 4. 25. . 5 0 g / L- (Ha second cam volume):.. touch internally at a rate 'and having as-medium layer, .. obtained in preparation j.22 F:. e, the ⁇ 3.1% Teiji
- the ratio of ⁇ —4 is .... :: ': ⁇ ' is a solution of .0 g .., 2 um volume) surface catalyst layer. , Body. :.
- Example 10 Example 10
- a catalyst obtained by supporting 2% platinum on the ceria / terbium oxide composite oxide obtained in Production Example 15 has an internal catalyst layer at a rate of 150 g / L (honeycomb volume).
- a honeycomb catalyst structure having a catalyst composed of SUZ-4 supporting Fe 2 0 3 1% obtained in Production Example 22 as a surface catalyst layer at a ratio of 50 g / L (honeycomb volume) was obtained. Comparative Example 1
- Pt (NH 3 ) 4 (N0 3 ) 2 aqueous solution (9.0% as platinum) 8.4 0 g is added to 10 OmL of ion-exchanged water to make an aqueous solution.
- it was calcined in air at 500 ° C. for 3 hours to obtain a catalyst powder in which 1% of platinum was supported on the alumina.
- Example 2 a catalyst in which 1% of platinum was supported on the alumina was used as an internal catalyst layer at a rate of 50 g / L (802 cam volume) and obtained in Production Example 12.
- cerium nitrate (Ce (N0 3 ) 3 ⁇ 6H 2 0) 151.37 g to 100 OmL of ion-exchanged water to make an aqueous solution.
- the obtained slurry was filtered, dried at 120 ° C. for 24 hours, and then calcined in air at 500 ° C. for 3 hours to obtain ceria powder (specific surface area 138 m 2 / g).
- Rhodium nitrate aqueous solution (9.0% as rhodium) 4.
- Barium carbonate was prepared from an aqueous solution of barium hydroxide and sodium carbonate, and 1% platinum was supported on this mixture of barium carbonate (B aCO 3 ) and r-alumina (weight ratio 8/2).
- catalyst powder was prepared.
- alumina and the above ⁇ 2 0 12 A 1 2 0 3 were mixed to prepare a mixture of lumina ⁇ 2 0 ⁇ 12 ⁇ 1 2 0 3 (weight ratio 9 / ⁇ ). • 1% platinum was supported to obtain a contact powder.
- the gas containing nitrogen oxides was reduced under the following conditions.
- the conversion rate (removal rate) from nitrogen oxides to nitrogen was determined by the chemical luminescence method.
- the test gas under lean conditions was prepared by injecting oxygen into the test gas under the above rich conditions, and the composition thereof was as follows.
- the catalytic reaction was carried out with the rich time (seconds) / lean (seconds) ranging from 3 (seconds) / 30 (seconds) to 12 (seconds) 20 (seconds), and the performance of each catalyst was examined.
- the catalyst according to the present invention has a high nitrogen oxide removal rate.
- the catalyst according to the comparative example generally has a low nitrogen oxide removal rate.
- the reaction temperature was 25 ° C to 400 ° C as shown in Fig. 2. Nitrogen formation is observed only immediately after the atmosphere of the treated gas is changed from lean condition to rich condition over this range. This is because N 0 2 adsorbed on the alkali compound (N Ox adsorbent) is reduced only by the reducing agent present in the gas at the time of the rich.
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Description
Claims
Priority Applications (4)
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CN2006800118384A CN101163537B (zh) | 2005-04-11 | 2006-04-06 | 用于催化还原氮氧化物的催化剂、催化剂结构体和用于催化还原氮氧化物的方法 |
CA002605255A CA2605255A1 (en) | 2005-04-11 | 2006-04-06 | Catalyst and catalyst structure for reduction of nitrogen oxides, and method for catalytic reduction of nitrogen oxides |
EP06731736A EP1875954A4 (en) | 2005-04-11 | 2006-04-06 | CATALYST FOR CATALYTIC REDUCTION OF NITROGEN OXIDE, CATALYST CONSTRUCTION AND METHOD FOR THE CATALYTIC REDUCTION OF NITROGEN OXIDE |
US11/918,222 US20090084090A1 (en) | 2005-04-11 | 2006-04-06 | Catalyst and Catalyst Structure for Reduction of Nitrogen Oxides, and Method for Catalytic Reduction of Nitrogen Oxides |
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US (1) | US20090084090A1 (ja) |
EP (1) | EP1875954A4 (ja) |
CN (1) | CN101163537B (ja) |
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CN107824186A (zh) * | 2017-11-17 | 2018-03-23 | 中国科学技术大学 | 一种氧化镨负载纳米钯复合材料及其制备方法 |
EP3680214B1 (de) * | 2019-01-14 | 2021-08-25 | Heraeus Deutschland GmbH & Co KG | Katalysatorsystem sowie verfahren zur katalytischen verbrennung von ammoniak zu stickstoffoxiden in einer mitteldruckanlage |
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EP2029260B2 (de) † | 2006-05-31 | 2019-03-06 | Umicore AG & Co. KG | Katalysator zur verminderung stickstoff-haltiger schadgase aus dem abgas von dieselmotoren |
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EP2213371A4 (en) * | 2007-10-29 | 2011-08-24 | Ict Co Ltd | CATALYST FOR REMOVING NITROGEN OXIDES AND METHOD FOR REMOVING NITROGEN OXIDES THEREWITH |
US8318630B2 (en) | 2007-10-29 | 2012-11-27 | Ict Co., Ltd. | Catalyst for removing nitrogen oxides and method for removing nitrogen oxides using the same |
JP5652848B2 (ja) * | 2007-10-29 | 2015-01-14 | ユミコア日本触媒株式会社 | 窒素酸化物除去用触媒およびそれを用いた窒素酸化物除去方法 |
US8703636B2 (en) | 2009-02-27 | 2014-04-22 | Corning Incorporated | Method of manufacturing a catalyst body by post-impregnation |
US9492811B2 (en) | 2009-02-27 | 2016-11-15 | Corning Incorporated | Zeolite and redox oxide combined catalyst body |
US10188985B2 (en) | 2009-02-27 | 2019-01-29 | Corning Incorporated | Zeolite and redox oxide combined catalyst body |
US10343117B2 (en) | 2009-02-27 | 2019-07-09 | Corning Incorporated | Ceria-zirconia-zeolite catalyst body |
Also Published As
Publication number | Publication date |
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EP1875954A4 (en) | 2011-06-22 |
US20090084090A1 (en) | 2009-04-02 |
CN101163537A (zh) | 2008-04-16 |
CA2605255A1 (en) | 2006-10-19 |
EP1875954A1 (en) | 2008-01-09 |
CN101163537B (zh) | 2011-12-14 |
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