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  • B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
  • B01D53/34—Chemical or biological purification of waste gases
  • B01D53/92—Chemical or biological purification of waste gases of engine exhaust gases
  • B01D53/94—Chemical or biological purification of waste gases of engine exhaust gases by catalytic processes
  • B01D53/9445—Simultaneously removing carbon monoxide, hydrocarbons or nitrogen oxides making use of three-way catalysts [TWC] or four-way-catalysts [FWC]
  • B01D53/945—Simultaneously removing carbon monoxide, hydrocarbons or nitrogen oxides making use of three-way catalysts [TWC] or four-way-catalysts [FWC] characterised by a specific catalyst
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  • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
  • B01J23/10—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of rare earths
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  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
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  • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
  • B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
  • B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
  • B01J23/56—Platinum group metals
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  • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
  • B01J37/0009—Use of binding agents; Moulding; Pressing; Powdering; Granulating; Addition of materials ameliorating the mechanical properties of the product catalyst
  • B01J37/0018—Addition of a binding agent or of material, later completely removed among others as result of heat treatment, leaching or washing,(e.g. forming of pores; protective layer, desintegrating by heat)
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  • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
  • B01J37/02—Impregnation, coating or precipitation
  • B01J37/03—Precipitation; Co-precipitation
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  • C01—INORGANIC CHEMISTRY
  • C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
  • C01F17/00—Compounds of rare earth metals
  • C01F17/20—Compounds containing only rare earth metals as the metal element
  • C01F17/206—Compounds containing only rare earth metals as the metal element oxide or hydroxide being the only anion
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  • C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
  • C01F17/00—Compounds of rare earth metals
  • C01F17/20—Compounds containing only rare earth metals as the metal element
  • C01F17/206—Compounds containing only rare earth metals as the metal element oxide or hydroxide being the only anion
  • C01F17/224—Oxides or hydroxides of lanthanides
  • C01F17/229—Lanthanum oxides or hydroxides
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  • C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
  • C01G25/00—Compounds of zirconium
  • C01G25/006—Compounds containing, besides zirconium, two or more other elements, with the exception of oxygen or hydrogen
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D2255/00—Catalysts
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  • B01D2255/206—Rare earth metals
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  • B01D2255/206—Rare earth metals
  • B01D2255/2063—Lanthanum
• • B—PERFORMING OPERATIONS; TRANSPORTING
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  • B01D—SEPARATION
  • B01D2255/00—Catalysts
  • B01D2255/20—Metals or compounds thereof
  • B01D2255/206—Rare earth metals
  • B01D2255/2066—Praseodymium
• • B—PERFORMING OPERATIONS; TRANSPORTING
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  • B01D2255/00—Catalysts
  • B01D2255/20—Metals or compounds thereof
  • B01D2255/206—Rare earth metals
  • B01D2255/2068—Neodymium
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  • B01D2255/20—Metals or compounds thereof
  • B01D2255/207—Transition metals
  • B01D2255/20715—Zirconium
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  • B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
  • B01J21/06—Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
  • B01J21/066—Zirconium or hafnium; Oxides or hydroxides thereof
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J35/00—Catalysts, in general, characterised by their form or physical properties
  • B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
  • B01J35/61—Surface area
  • B01J35/613—10-100 m2/g
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  • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
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  • C01P2006/13—Surface area thermal stability thereof at high temperatures
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
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  • Y02T10/10—Internal combustion engine [ICE] based vehicles
  • Y02T10/12—Improving ICE efficiencies

Definitions

• the present invention relates to a composition based on zirconium oxide, on an additive selected from the oxides of praseodymium, lanthanum and neodymium, its method of preparation and its use in a catalytic system.
• Multifunctional catalysts are used at the present time for treating exhaust gases of internal combustion engines (automobile postcombustion catalysis).
• Multifunctional catalysts are catalysts capable not only of obtaining the oxidation of the carbon monoxide and hydrocarbons present in the exhaust gases, but also of reducing the nitrogen oxides also present in these gases (“three-way” catalysts).
• Catalysts based on zirconium oxide or cerium oxide are known today as particularly advantageous for this type of reaction.
• these catalysts must have a high specific surface area, and there is a continuing search for catalysts which can be used at increasingly high temperatures, and, for this purpose, have a more stable specific surface area.
• the composition of the invention is based on zirconium oxide and is characterized in that it further comprises at least one additive selected from the oxides of praseodymium, lanthanum and neodymium, and in that it has a specific surface area of at least 29 m 2 /g after calcination for 10 hours at 1000° C.
• the composition of the invention thereby has the advantage of preserving a high specific surface area at a temperature of 1000° C. or even more. Furthermore, the catalysts based on this composition may also have high efficiency at low temperature even with a low precious metal content.
• specific surface area means the BET specific surface area determined by nitrogen adsorption according to standard ASTM D 3663-78 established using the Brunauer-Emmett-Teller method described in the periodical The Journal of the American Chemical Society, 60, 309 (1938).
• the periodic table of elements referred to in the present description is the one published in the Supplis Bulletin de la cios Chimique de France No. 1 (January 1966).
• Rare earth means elements of the group consisting of yttrium and the elements of the periodic table with atomic numbers of 57 to 71 inclusive.
• compositions of the invention are the nature of their components and their specific surface area.
• compositions of the invention are based on zirconium oxide ZrO 2 , this oxide being the essential or majority component.
• the compositions further comprise at least one additive, which constitutes the remainder of the composition and which is present in the form of an oxide, this additive being selected from praseodymium, lanthanum and neodymium. It should be observed here that the invention obviously covers the case of compositions comprising a combination of additives.
• the additive content does not exceed 50% by weight, the zirconium oxide constituting at least 50% by weight of the composition.
• This content is expressed as the weight of oxide of the additive or of all the additives in the case of compositions containing several additives, with respect to the weight of the composition as a whole (zirconium oxide plus additive oxide(s)).
• This additive content may vary in a wide range and more particularly between 5% and 40% and most particularly between 10% and 40%. This content may be quite particularly between 10% and 30%.
• compositions of the invention may further comprise aluminum oxide Al 2 O 3 .
• the aluminum content (Al 2 O 3 weight % with respect to the total composition) is generally not more than 20%, and, preferably, is between 1% and 10%.
• compositions of the invention may further comprise silica in proportions identical to those given above for alumina.
• compositions of the invention are their high specific surface area at high temperature.
• this area is at least 29 m 2 /g, after calcination for 10 hours at 1000° C. Under the same calcination conditions, this area may be at least 35 m 2 /g, or even at least 40 m 2 /g and even more preferably at least 50 m 2 /g. Areas of about 60 m 2 /g may be reached.
• compositions of the invention preserve high surface areas.
• these compositions may have a specific surface area of at least 10 m 2 /g or even at least 15 m 2 /g. Areas of about 20 m 2 /g may be obtained.
• compositions of the invention may still have a specific surface area of at least 2 m 2 /g and more particularly of at least 3 m 2 /g.
• the compositions may have a specific surface area of at least 45 m 2 /g, more particularly of at least 50 m 2 /g and preferably of at least 55 m 2 /g and even more preferably of at least 70 m 2 /g. Areas of about 80 m 2 /g may be obtained.
• compositions of the invention may in certain cases be in the form of solid solutions of the additive in the zirconium oxide.
• compositions reveal the existence of a single phase corresponding to that of a zirconium oxide crystallized in the cubic system or in the quadratic system, thereby reflecting the incorporation of the additive in the crystal lattice of the zirconium oxide, and hence the production of a true solid solution.
• the compositions may also be in the form of a mixture of phases, particularly in the case of high additive contents, that is of at least 40%.
• compositions of the invention also have a specific porosity. They in fact contain mesopores, that is pores between 10 nm and 500 nm in size, even after calcination at high temperature. These size values are obtained by mercury porosimetry (analysis performed with an Autopore 9410 porosimeter, manufactured by Micromeritics, comprising two low pressure stations and one high pressure station). These mesopores may contribute a high proportion of the total pore volume, for example, they may contribute at least 30%, more particularly at least 40% of the total pore volume.
• compositions of the invention may have a very low sulfate anion content. This content is generally not more than 100 ppm and preferably not more than 50 ppm (SO 4 ⁇ /total composition weight ratio).
• the first step of the method thus consists in preparing a mixture in liquid medium of a zirconium compound, a compound of the additive and, optionally, a compound of aluminum or silicon.
• the mixing is generally carried out in a liquid medium which is preferably water.
• the compounds are preferably soluble compounds. This may be the case particularly of salts of zirconium, of the additive and of aluminum. These compounds may be selected for example from nitrates, acetates or chlorides.
• zirconyl nitrate As examples, mention can be made of zirconyl nitrate or zirconyl chloride. Zirconyl nitrate is the most commonly used.
• a sol as a starting compound for zirconium.
• Sol means any system consisting of fine solid particles of colloidal size, that is, dimensions of between 1 nm and about 500 nm, based on a zirconium compound, this compound generally being a zirconium oxide and/or a zirconium oxide hydrate, in suspension in an aqueous liquid phase, said particles also optionally containing residual quantities of bound or adsorbed ions such as, for example, nitrates, acetates, chlorides or ammoniums. It may be observed that in such a sol, the zirconium may be entirely in colloidal form, or simultaneously in the form of ions and colloids.
• silicon compounds use can be made of a silicate of an alkali element, for example sodium, a silicon alkoxide or an alkylsiliconate of an alkali element such as sodium or potassium, and mention can be made of potassium methyl siliconate as an example.
• a solution of silicic acid or a precipitated silica which can be obtained from the preceding precursors.
• the silica may be present in the form of a sol or a suspension.
• the starting mixture may be obtained either from compounds initially in the solid state which are introduced subsequently into the bottom of a water tank, for example, or directly from solutions of these compounds followed by mixing of said solutions in any order.
• said mixture is contacted with a basic compound.
• Products of the hydroxide type can be used as a base or basic compound.
• Mention can be made of alkali or alkaline earth hydroxides. Use can also be made of secondary, tertiary or quaternary amines. However, amines and aqueous ammonia may be preferred insofar as they decrease the risk of pollution by alkali or alkaline earth cations. Mention can also be made of urea.
• the basic compound is generally used in the form of an aqueous solution.
• the method for contacting the mixture and the solution that is, the order of introduction thereof, is not critical. However, this contacting can be obtained by introducing the mixture into the solution of the basic compound.
• the contacting or the reaction between the mixture and the solution can be carried out in a single step, gradually or continuously, and it is preferably carried out with stirring. It is preferably carried out at ambient temperature (20-25° C.).
• the next step (c) of the method is the heating of the precipitate in liquid medium.
• This heating can be carried out directly on the reaction medium obtained after reaction with the basic compound or on a suspension obtained after separation of the precipitate from the reaction medium, optional washing and replacement of the precipitate in water.
• the temperature to which the medium is heated is at least 100° C. and even more particularly at least 130° C.
• the heating operation can be carried out by introducing the liquid medium into a closed chamber (closed reactor of the autoclave type). Under the temperature conditions given above, and in aqueous medium, as an illustration, the pressure in the closed reactor may vary between a value above 1 bar (10 5 Pa) and 165 bar (1.65 ⁇ 10 7 Pa), preferably between 5 bar (5 ⁇ 10 5 ) and 165 bar (1.65 ⁇ 10 7 Pa).
• the heating can also be carried out in an open reactor for temperatures close to 100° C.
• the heating can be carried out either in air, or in an inert gas atmosphere, preferably nitrogen in the latter case.
• the heating time may vary within wide limits, for example between 1 and 48 hours, preferably between 2 and 24 hours.
• the temperature rise rate is not critical, and the desired reaction temperature can thereby be reached by heating the medium, for example, for between 30 minutes and 4 hours, these values being given entirely for guidance.
• the precipitate obtained after the heating step and optionally a washing can be replaced in suspension in water, and the medium thereby obtained again heated.
• This second heating is carried out under the same conditions as those described for the first.
• the next step (d) of the method consists in adding, to the precipitate from the preceding step, a compound selected from anionic surfactants, nonionic surfactants, polyethyleneglycols and carboxylic acids and salts thereof.
• anionic surfactants mention can be made of ethoxycarboxylates, ethoxylated fatty acids, sarcosinates, phosphate esters, sulfates such as alcohol sulfates, ether alcohol sulfates and alkanolamide sulfate ethoxylates, sulfonates such as sulfosuccinates, alkylbenzene or alkylnaphthalenesulfonates.
• sulfates such as alcohol sulfates, ether alcohol sulfates and alkanolamide sulfate ethoxylates
• sulfonates such as sulfosuccinates, alkylbenzene or alkylnaphthalenesulfonates.
• nonionic surfactants mention can be made of acetylenic surfactants, alcohol ethoxylates, alkanolamides, amine oxides, ethoxylated alkanolamides, long chain ethoxylated amines, ethylene oxide/propylene oxide copolymers, derivatives of sorbiatan, ethylene glycol, propylene glycol, glycerol, polyglyceryl esters and their ethoxylated derivatives, alkylamines, alkylimidazolines, ethoxylated oils and alkylphenol ethoxylates. Mention can be made particularly of products sold under the trademarks IGEPAL®, DOWANOL®, RHODAMOX® and ALKAMIDE®.
• carboxylic acids use can be made particularly of aliphatic mono- or dicarboxylic acids, and among them more particularly saturated acids. Use can also be made of fatty acids and more particularly saturated fatty acids. Mention can thus be made particularly of formic, acetic, propionic, butyric, isobutyric, valeric, caproic, caprylic, capric, lauric, myristic, palmitic acids.
• dicarboxylic acids mention can be made of oxalic, malonic, succinic, glutaric, adipic, pimelic, suberic, azelaic and sebacic acids.
• Carboxylic acid salts can also be used, particularly ammoniacal salts.
• lauric acid and ammonium laurate For example, mention can be made more particularly of lauric acid and ammonium laurate.
• Carboxymethylated fatty alcohol ethoxylates means products consisting of ethoxylated or propoxylated fatty alcohols comprising a —CH 2 —COOH group at the end of the chain.
• R 1 denotes a saturated or unsaturated carbon chain, of which the length is generally not more than 22 carbon atoms, preferably at least 12 carbon atoms;
• R 2 , R 3 , R 4 and R 5 may be identical and represent hydrogen or R 2 may represent a CH 3 group and R 3 , R 4 and R 5 represent hydrogen;
• n is a nonzero integer of up to 50 and more particularly of between 5 and 15, these values being inclusive.
• a surfactant may consist of a mixture of products with the above formula, for which R 1 may be saturated and unsaturated respectively, or products comprising both —CH 2 —CH 2 —O— and —C(CH 3 )—CH 2 —O— groups.
• the surfactant can be added in two ways. It may be added directly to the suspension of precipitate issuing from the preceding heating step (c). It may also be added to the solid precipitate after it has been separated by any known means from the medium in which the heating has taken place.
• the quantity of surfactant used is generally between 5% and 100%, more particularly between 15% and 60%.
• step (d) just described it is possible, on completion of step (d) just described, to grind the precipitate.
• This grinding can be carried out in various ways.
• a first way is to carry out a high energy grinding of the wet grinding type. Such a grinding is carried out on a wet precipitate which has, for example, been obtained after adding the surfactant to the solid precipitate. Wet grinding can be carried out in a ball mill, for example.
• a second way is to carry out grinding at medium energy by subjecting a suspension of the precipitate to shearing, for example by using a colloidal grinder or a turbomixer.
• This suspension may be an aqueous suspension that has been obtained after replacing the precipitate obtained on completion of the steps (d) in a dispersion in water.
• the precipitate recovered is then calcined.
• This calcination serves to develop the crystallinity of the product formed, and it may also be adjusted and/or selected according to the subsequent temperature of use reserved for the composition according to the invention, and taking account of the fact that the specific surface area of the product decreases with rising calcination temperature.
• Such a calcination is generally carried out in air, but a calcination carried out, for example, in inert gas or controlled (oxidizing or reducing) atmosphere is obviously not excluded.
• the calcination temperature is generally limited to a range of values of between 500° C. and 1100° C., more particularly between 600° C. and 900° C.
• compositions of the invention as described above or those obtained in the method previously examined are in the form of powders, but they can optionally be shaped into granules, beads, cylinders or honeycombs of variable dimensions.
• compositions of the invention can be used as catalysts or catalyst supports.
• the invention also relates to catalytic systems comprising the compositions of the invention.
• these compositions may thus be applied to any support commonly used in the field of catalysis, that is, particularly thermally inert supports.
• This support may be selected from alumina, titanium dioxide, cerium oxide, silica, spinels, zeolites, silicates, crystalline aluminum silicate phosphates, crystalline aluminum phosphates.
• compositions may also be used in catalytic systems comprising a wash coat with catalytic properties and based on these compositions, on a substrate of the type, for example, of a metal or ceramic monolith.
• the wash coat may also comprise a support of the type of those mentioned above. This wash coat is obtained by mixing the composition with the support to form a suspension which can then be deposited on the substrate.
• transition metals means elements of groups IIIA to IIB of the periodic table.
• transition metals mention can be made more particularly of iron, manganese and copper, as well as precious metals, such as platinum, rhodium, palladium, silver or iridium.
• precious metals such as platinum, rhodium, palladium, silver or iridium.
• the metals may be incorporated in the compositions by impregnation.
• the contents of abovementioned metal in the compositions correspond to the contents commonly used in catalysts to obtain catalytic activity.
• this content is not higher than 5%, particularly not higher than 1%. It may more particularly be not higher than 0.5% and even not higher than 0.25%. Contents above 5% are generally not economically advantageous. These contents are expressed as a weight percentage of metal with respect to the composition.
• the catalytic systems and more particularly the compositions of the invention can find numerous applications. They are thus particularly suitable for, and hence usable in, the catalysis of various reactions such as, for example, dehydration, hydrosulfurization, hydrodenitrification, desulfurization, hydrodesulfurization, dehydrohalogenation, reforming, steam reforming, cracking, hydrocracking, hydrogenation, dehydrogenation, isomerization, dismutation, oxychlorination, dehydrocyclization of hydrocarbons or other organic compounds, oxidation and/or reduction reactions, the Claus reaction, the treatment of exhaust gases of internal combustion engines, demetallation, methanation, shift conversion, catalytic oxidation of soot emitted by internal combustion engines such as lean burn diesel or gasoline engines.
• various reactions such as, for example, dehydration, hydrosulfurization, hydrodenitrification, desulfurization, hydrodesulfurization, dehydrohalogenation, reforming, steam reforming, cracking, hydrocracking, hydrogenation, de
• the catalytic systems and more particularly the compositions of the invention are particularly appropriate for the treatment of exhaust gases of internal combustion engines such as lean burn diesel or gasoline engines.
• This treatment may be more precisely a treatment to remove NOx by a continuous reaction with the hydrocarbons in a lean mixture (HC-DeNOx catalysis).
• the invention also relates to a method for treating exhaust gases of internal combustion engines, which is characterized in that a catalytic system such as described above, or a composition according to the invention and such as described above is used as the catalyst.
• compositions of the invention can be used in combination with compositions based on cerium oxide stabilized by additives such as zirconium oxide or a rare earth oxide, zirconium oxide and the rare earth oxide being usable in combination in this case, or in combination with compositions based on zirconium oxide, this oxide also optionally being doped or stabilized by a rare earth, such as cerium particularly.
• This example concerns a composition with 60% zirconium and 40% praseodymium, these proportions being expressed as weight percentages of the oxides ZrO 2 and Pr 6 O 11 .
• the nitrate solution is introduced in one hour into the reactor with constant stirring.
• the solution obtained is placed in a stainless steel autoclave equipped with a stirrer.
• the temperature of the medium is raised to 150° C. with stirring for 2 hours.
• the suspension thus obtained is filtered on a Büchner funnel. A precipitate containing 19% by weight of oxide is recovered.
• an ammonium laurate gel is prepared under the following conditions: 250 g of lauric acid are introduced into 135 ml of aqueous ammonia (12 mol/l) and 500 ml of distilled water, and the mixture blended using a spatula.
• the product obtained is then heated to 500° C. for 4 hours in steps.
• the XR analyses show that between 900° C. and 1000° C., the product has a majority cubic phase and a minority quadratic phase.
• the total pore volume measured is 0.81 ml/g of oxide.
• the pores between 10 nm and 500 nm in diameter constitute 39% of the total pore volume.
• This example concerns a composition with 85% zirconium and 15% praseodymium, these proportions being expressed as weight percentages of the oxides ZrO 2 and Pr 6 O 11 .
• the nitrate solution is introduced in one hour into the reactor with constant stirring.
• the solution obtained is placed in a stainless steel autoclave equipped with a stirrer.
• the temperature of the medium is raised to 150° C. with stirring for 2 hours.
• the suspension thus obtained is filtered on a Büchner funnel. A precipitate containing 17.9% by weight of oxide is recovered.
• an ammonium laurate gel is prepared under the following conditions: 250 g of lauric acid are introduced into 135 ml of aqueous ammonia (12 mol/l) and 500 ml of distilled water, and the mixture blended using a spatula.
• the product obtained is then heated to 500° C. for 4 hours in steps.
• the XR analyses show that between 900° C. and 1000° C., the product has a single quadratic phase.
• This example concerns a composition containing 90% zirconium and 10% praseodymium, these proportions being expressed as weight percentages of the oxides ZrO 2 and Pr 6 O 11 .
• the surface characteristics are given in Table 3 below.
• the XR analyses show that between 900° C. and 1000° C., the product has a single quadratic phase.
• This example concerns a composition containing 90% zirconium and 10% lanthanum, these proportions being expressed as weight percentages of the oxides ZrO 2 and La 2 O 3 .
• This example concerns a composition containing 90% zirconium and 10% neodymium, these proportions being expressed as weight percentages of the oxides ZrO 2 and Nd 2 O 3 .
• This example describes a catalytic test for a catalyst prepared using a composition according to the invention.
• the catalyst containing 0.1% by weight of metal rhodium element with respect to the total weight of catalyst is prepared by wet impregnation of rhodium nitrate on the product of Example 3 obtained after 4 h of calcination at 500° C.
• the impregnated product is then subjected to slow evaporation, drying, and finally, calcination in air for 4 h at 500° C.
• the catalyst in powder form is then aged for 6 hours at 1100° C. in a redox mixture (alternating streams of 5 minutes of 1.8% CO and 10% H 2 0 , and of 1.8% O 2 and 10% H 2 O).
• the catalyst is then aged in a quartz tubular fired heater, traversed by the gas stream.
• Catalyst weight 20 mg (grain size fraction 100-200 microns) diluted with 150 mg of SiC.
• composition of the gases is given in Table 4 below.
• Fuel-Air Ratio Component 0.979% by volume 1.024% by volume CO 2 14.00 14.00 H 2 O 10.00 10.00 CO 0.40 1.40 O 2 0.80 0.40 C 3 H 6 0.0375 0.0375 C 3 H 8 0.0125 0.0125 NO 0.095 0.095 N 2 Complement to 100 Complement to 100
• the initiation temperature at 20% conversion for NO is 345° C., for C 3 H 6 it is 350° C. Hence these are low temperatures in both cases.
• the half-conversion (50% conversion) temperature for NO and C 3 H 6 is only 360° C. 100% of NO and C 3 H 6 are converted before 400° C.
• the initiation temperatures at 20% conversion for NO, for C 3 H 6 and for CO are 310° C., 325° C. and 285° C. respectively. Moreover, for C 3 H 6 80% conversion is obtained at 500° C.
• a composition is prepared based on zirconium and cerium oxides, with a specific surface area stabilized by lanthanum and neodymium oxides.
• This composition answers to the formula ZrO 2 /CeO 2 /La 2 O 3 /Nd 2 O 3 with respective weight proportions of these oxides of 75/20/2.5/2.5.
• the method of preparation is identical to the one described in Example 2. However, the precipitate is not mixed with the surfactant, but is directly calcined.
• the product obtained after calcination for 4 hours at 1000° C. has a specific surface area of 44 m 2 /g and, after calcination for 4 hours at 1100° C., a specific surface area of 18 m 2 /g.
• a catalyst containing 0.1% by weight of metal rhodium element with respect to the total weight of catalyst is also prepared by the wet impregnation of rhodium nitrate on the composition prepared as described above and obtained after 4 hours of calcination at 500° C.
• This catalyst thereby prepared is subjected to the same aging at 1100° C. and the same test as described above in Example 6.
• Table 5 gives the results for initiation temperatures at 20% (Ta) for the products of Examples 6 and 7.
• the initiation temperatures are much higher in the case of the product of the comparative example.
• This example concerns a composition containing 80% zirconium and 20% praseodymium, these proportions being expressed as weight percentages of the oxides ZrO 2 and Pr 6 O 11 .
• the nitrate solution is introduced in one hour into the reactor with constant stirring.
• the solution obtained is placed in a stainless steel autoclave equipped with a stirrer.
• the temperature of the medium is raised to 150° C. for 4 hours with stirring.
• the product obtained is then heated to 700° C. for 4 hours in steps.
• the XR analyses show that between 900° C. and 1000° C., the product has a majority cubic phase and a minority quadratic phase.
• This example concerns a composition containing 90% zirconium and 10% praseodymium, these proportions being expressed as weight percentages of the oxides ZrO 2 and Pr 6 O 11 .
• Example 2 The same procedure is followed as in Example 1, with two exceptions: the surfactant is added in the form of lauric acid (33 grams) directly to the suspension issuing from the autoclave and after cooling, and the initial calcination is carried out at 800° C. for 3 hours.
• the surfactant is added in the form of lauric acid (33 grams) directly to the suspension issuing from the autoclave and after cooling, and the initial calcination is carried out at 800° C. for 3 hours.
• the total pore volume measured is 1.32 ml/g of oxide.
• the pores between 10 nm and 500 nm in diameter constitute 48% of the total pore volume.

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