WO2023198577A1 - Système de gaz d'échappement pour moteurs à combustion interne fonctionnant principalement de manière stœchiométrique, comprenant un catalyseur pour réduire les émissions d'ammoniac - Google Patents

Système de gaz d'échappement pour moteurs à combustion interne fonctionnant principalement de manière stœchiométrique, comprenant un catalyseur pour réduire les émissions d'ammoniac Download PDF

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Publication number
WO2023198577A1
WO2023198577A1 PCT/EP2023/059087 EP2023059087W WO2023198577A1 WO 2023198577 A1 WO2023198577 A1 WO 2023198577A1 EP 2023059087 W EP2023059087 W EP 2023059087W WO 2023198577 A1 WO2023198577 A1 WO 2023198577A1
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WIPO (PCT)
Prior art keywords
exhaust system
ammonia
oxide
catalyst
exhaust gas
Prior art date
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PCT/EP2023/059087
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German (de)
English (en)
Inventor
Julius KOEGEL
Massimo Colombo
Martin Roesch
Sonja Buchberger
Marcus Schmidt
Original Assignee
Umicore Ag & Co. Kg
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Publication date
Priority claimed from DE102023101768.3A external-priority patent/DE102023101768A1/de
Application filed by Umicore Ag & Co. Kg filed Critical Umicore Ag & Co. Kg
Publication of WO2023198577A1 publication Critical patent/WO2023198577A1/fr

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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • 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
    • B01D53/9404—Removing only nitrogen compounds
    • B01D53/9436—Ammonia
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • 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]
    • B—PERFORMING OPERATIONS; TRANSPORTING
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    • 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
    • B01D53/9459—Removing one or more of nitrogen oxides, carbon monoxide, or hydrocarbons by multiple successive catalytic functions; systems with more than one different function, e.g. zone coated catalysts
    • B01D53/9463—Removing one or more of nitrogen oxides, carbon monoxide, or hydrocarbons by multiple successive catalytic functions; systems with more than one different function, e.g. zone coated catalysts with catalysts positioned on one brick
    • B01D53/9468—Removing one or more of nitrogen oxides, carbon monoxide, or hydrocarbons by multiple successive catalytic functions; systems with more than one different function, e.g. zone coated catalysts with catalysts positioned on one brick in different layers
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    • B01D53/9459—Removing one or more of nitrogen oxides, carbon monoxide, or hydrocarbons by multiple successive catalytic functions; systems with more than one different function, e.g. zone coated catalysts
    • B01D53/9477—Removing one or more of nitrogen oxides, carbon monoxide, or hydrocarbons by multiple successive catalytic functions; systems with more than one different function, e.g. zone coated catalysts with catalysts positioned on separate bricks, e.g. exhaust systems
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    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
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    • F01N2570/00—Exhaust treating apparatus eliminating, absorbing or adsorbing specific elements or compounds
    • F01N2570/18—Ammonia

Definitions

  • the present invention is aimed at an exhaust system for reducing exhaust gases and in particular ammonia emissions in the exhaust system of a predominantly stoichiometrically operated spark ignition engine.
  • Spark ignition engines or gasoline engines powered by gasoline or natural gas are cleaned in conventional processes using three-way catalysts (TWC). These are able to simultaneously convert the engine's three main gaseous pollutants, namely hydrocarbons, carbon monoxide and nitrogen oxides, into harmless components.
  • Stoichiometric means that, on average, there is as much air available to burn the fuel present in the cylinder as is required for complete combustion.
  • the combustion air ratio ⁇ (A/F ratio; air/fuel ratio) relates the air mass m L,tats actually available for combustion to the stoichiometric air mass m L,st : If ⁇ ⁇ 1 (e.g. 0.9) this means “lack of air”, one speaks of a rich exhaust gas mixture, ⁇ > 1 (e.g. 1.1) means “excess air” and the exhaust gas mixture is considered lean designated.
  • ⁇ 1.1 means that 10% more air is present than would be necessary for the stoichiometric reaction. The same applies to the exhaust gases from internal combustion engines.
  • the catalytically active materials used in the known three-way catalysts are generally platinum group metals, in particular platinum, palladium and rhodium, which are present, for example, on ⁇ -aluminum oxide as a support material.
  • three-way catalysts contain oxygen storage materials, for example cerium/zirconium mixed oxides. In the latter, cerium oxide, a rare earth metal oxide, is the fundamental component for oxygen storage. In addition to zirconium oxide and cerium oxide, these materials can contain additional components such as other rare earth metal oxides or alkaline earth metal oxides.
  • Oxygen storage materials are made by Application of catalytically active materials such as platinum group metals activates and thus also serves as a carrier material for the platinum group metals.
  • Compliance with the strict emission values for ammonia requires the use of a storage material to store NH 3 during the rich operating conditions of the combustion engine, particularly in low and medium temperature ranges. engines, as the ammonia is mainly formed under these exhaust gas conditions. The stored ammonia is then converted during lean operating points by oxidation on a layer containing precious metal and/or as part of an SCR reaction. The aim here is to achieve the lowest possible selectivity to N 2 O.
  • a special requirement for the catalysts considered here is the high aging stability of the materials used: In addition to the stability against lean gas conditions, their use in the exhaust system of stoichiometrically operated internal combustion engines also requires that they also be used in the exhaust gas with rich or stoichiometric ric composition are stable under hydrothermal exhaust gas conditions.
  • the use of catalysts, which preferentially convert ammonia into nitrogen, has already been discussed, particularly in the diesel sector or for use in lean-burning DI petrol engines (US5120695; EP1892395A1; EP1882832A2; EP1876331A2; WO12135871A1; US2011271664AA; WO1111091 9A1, EP3915679A1).
  • CNG “Compressed Natural Gas”
  • SCR SCR catalytically active component
  • a component that catalyzes the oxidation of ammonia They are usually located in the underbody at the last point of the exhaust system. If for oxidation of the If there are not enough nitrogen oxides in the system from the stored ammonia, the ammonia can also be converted into nitrogen via the ASC with the oxygen present.
  • the corresponding limit values for NH 3 and N 2 O should be safely adhered to in addition to the traditional ones for CO, HC and NOx.
  • the system should also be robust and agile in order to be able to withstand the working conditions in the exhaust system of a corresponding automobile for a sufficient period of time.
  • Claims 2 - 11 relate to preferred embodiments of the exhaust system and can accordingly also be applied to the method according to the invention.
  • an exhaust system for reducing harmful exhaust gas components from internal combustion engines in particular predominantly stoichiometrically operated gasoline engines, having a first three-way catalytic converter and, downstream of this, a catalyst for reducing ammonia emissions, which has the following components: - a first component comprising a transition metal-exchanged zeolite and/or zeotypes for storing ammonia in a first layer; - a second component with an OSC-free noble metal catalyst and / or an OSC-containing noble metal catalyst in a second layer, the first layer and the second layer being separated from each other by an inert layer, the solution is relatively easy, but no less surprising the task given.
  • the system according to the invention is characterized by extremely good performance in terms of reducing CO, HC and NOx emissions as well as NH3 and N2O emissions. It reacts well to the dynamic requirements in the exhaust system of a gasoline engine and is robust enough to meet these requirements for a sufficient period of time.
  • the components of the catalyst for reducing ammonia emissions are applied to a carrier, preferably to a flow-through substrate, using a coating step familiar to those skilled in the art (DE102019100099A1 and the literature cited there).
  • a filter substrate such as a wall flow filter is also possible in this context.
  • Flow-through substrates are catalyst supports that are common in the prior art and can consist of metal, for example WO17153239A1, WO16057285A1, WO15121910A1 and the literature cited therein) or ceramic materials.
  • “Corrugated substrates” can also be viewed as flow-through substrates. These are known to those skilled in the art as carriers made of corrugated sheets made of inert materials. Suitable inert materials are, for example, fibrous materials with an average fiber diameter of 50 to 250 ⁇ m and an average fiber length of 2 to 30 mm. Fibrous heat-resistant materials made of silicon dioxide, especially glass fibers, are preferred. However, refractory ceramics such as cordierite, silicon carbite or aluminum titanate etc.
  • the number of carrier channels per area is characterized by the cell density, which is usually between 300 and 900 cells per square inch (cells per square inch, cpsi).
  • the wall thickness of the channel walls for ceramics is between 0.5 – 0.05 mm.
  • the total amount of coating in the catalyst to reduce ammonia emissions is selected so that the catalyst according to the invention is used as efficiently as possible overall.
  • the total amount of coating (solids content) per carrier volume (total volume of the carrier) can be between 105 and 600 g/L, in particular between 150 and 400 g/L.
  • the first component is preferably used in an amount of 50 to 350 g/L, in particular between 120 and 250 g/L, particularly preferably about 145 - 230 g/L of carrier volume.
  • the second component is preferably used from 50 to 350 g/L, in particular between 120 and 250 g/L, particularly preferably from about 145 - 230 g/L carrier volume.
  • the inert layer preferably has a loading of 10 g/L - 120 g/L, more preferably 20 g/L - 75 g/L.
  • the components are present as separate coatings one above the other on the substrate.
  • the first component is in the first layer, the second component in the second. It is preferred if the second layer lies completely above the first and completely covers it.
  • the reverse arrangement is also possible.
  • the first layer does not protrude over the second layer at any end out.
  • the two coatings with the respective components are of the same length (Fig.2).
  • the length of the layers can be chosen by the specialist. They are preferably located on a flow-through substrate and here take up a length of at least 10% and a maximum of 100%, more preferably 20% - 90%, extremely preferably 30% - 80% of the substrate length. In this case, a coating that lies above another comes into contact with the exhaust gas first before the latter. It has surprisingly proven to be advantageous if there is a thin, additional, separate layer between the two layers just mentioned. The person skilled in the art is guided by the coating methods mentioned above for their production.
  • This thin layer which is between 5 ⁇ m and 200 ⁇ m, preferably between 10 ⁇ m and 150 ⁇ m thick, helps to further increase the aging stability of the catalyst to reduce ammonia emissions.
  • a disadvantage of the known systems for reducing ammonia emissions can be that the transition metals in the first component, such as iron and/or copper, tend to, after a long period of use in the exhaust system of a predominantly stoichiometrically operated internal combustion engine, Diffuse into the ammonia oxidation component and poison it. The result is a lower activity of the ammonia-storing and oxidative components.
  • Suitable materials for this layer are, in particular, those selected from the group consisting of aluminum oxide, silicon oxide, titanium oxide, zirconium oxide, zeolites or mixtures of one or more of these.
  • a layer made of aluminum oxide is particularly preferred in this context.
  • the inert layer preferably contains no SiO 2 or zeolites.
  • the inert layer is preferably located on the substrate in the same length between the first layer and the second layer.
  • a first component of the catalyst for reducing ammonia emissions consists of zeolites and/or zeotypes for storing ammonia. In principle, those skilled in the art are familiar with the zeolites and zeotypes available for this purpose from the diesel sector.
  • zeolites or zeotypes work is based on the fact that they can temporarily store ammonia in operating states of the exhaust gas purification system in which ammonia is produced, for example, by overreduction of nitrogen oxides via a three-way catalytic converter installed on the upstream side, but this is not converted by other conventional three-way catalytic converters. This can happen, for example due to a lack of oxygen or insufficient oxygen Operating temperatures.
  • the ammonia stored in this way can then be stored out when the operating state of the exhaust gas purification system changes and subsequently or directly converted, for example when sufficient oxygen or nitrogen oxides are present.
  • zeolites and zeotypes are present in the first component of the catalyst to reduce ammonia emissions.
  • zeolites or zeotypes can be divided into different classes. Zeolites are then divided, for example, according to their channel system and their framework structure. For example, laumontite and mordenite are classified as zeolites, which have a one-dimensional system of channels. Your channels have no connection with each other. Zeolites with a two-dimensional channel system are characterized by the fact that their channels are connected to one another in a kind of layered system. A third group has a three-dimensional framework structure with cross-layer connections between the channels.
  • zeolites or zeotypes are preferably used [Ch. Baerlocher, WM Meier and DH Olson, Atlas of Zeolite Framework Types, Elsevier, 2001].
  • zeolite means porous materials with a lattice structure of corner-connected AlO 4 and SiO 4 tetrahedra according to the general formula (WM Meier, Pure & Appl.
  • zeolite thus comprises a network made up of tetrahedra that encloses channels and cavities.
  • zeotype is understood to mean a zeolite-like compound that has the same structural type as a naturally occurring or synthetically produced zeolite compound, but which differs from such compounds in that the corresponding cage structure is not made up exclusively of aluminum and silicon framework atoms .
  • the aluminum and/or silicon framework atoms are proportionally replaced by other trivalent, quadrivalent or pentavalent framework atoms such as B(III), Ga(III), Ge(IV), Ti(IV) or P(V) replaced.
  • the most commonly used in practice is the replacement of aluminum and/or Silicon framework atoms are replaced by phosphorus atoms, for example in the silicon aluminum phosphates or in the aluminum phosphates, which crystallize in zeolite structure types.
  • suitable zeolites come from the group of two-dimensional or three-dimensional zeolites/zeotypes.
  • They preferably belong to the structure types ACO, AEI, AEN, AFN, AFT, AFX, ANA, APC, APD, ATT, BEA, BIK, CDO, CHA, DDR, DFT, EAB, EDI, EPI, ERI, ESV, ETL, DER , GIS, GOO, IHW, ITE, ITW, LEV, KFI, MER, MON, NSI, OWE, PAU, PHI, RHO, RTH, SAT, SAV, SIV, THO, TSC, UEI, UFI, VNI, YUG, ZON at.
  • the zeolites or zeotypes in the car exhaust gas catalyst according to the invention are selected from the group AEI, AFT, AFX, CHA, DDR, ERI, ESV, ETL, FER, KFI, LEV, UFI and the corresponding zeotypes of these structural types, such as e.g.: SAPO. Mixtures of the same can also be present. Zeolites or zeotypes can also be classified according to their pore structure. A distinction is made between small-pore, medium-pore and large-pore zeolites. The extra-large pore zeolites are of academic interest. Small-pore zeolites are those with a largest ring size of 8 tetrahedral units.
  • CHA, AEI, AFX, BIK, DDR, ERI, LEV or LTA are particularly preferred as small-pore zeolites or zeotypes for storing ammonia.
  • CHA is extremely preferred in this context.
  • Large-pore zeolites or zeotypes for storing ammonia are preferably selected from the group consisting of BEA, FAU or MOR. BEA is particularly preferred in this context.
  • a well-known property of the ion-exchanged large-pore zeolites is their ability to store hydrocarbons, which gives the formulated ammonia storage the properties of a so-called hydrocarbon trap.
  • hydrocarbon trap During the cold start, incoming hydrocarbons can be captured, which then desorb at a higher temperature and can be converted via the then active three-way catalysts or oxidation catalysts.
  • the aging stability of the zeolites or zeotypes used in the exhaust system of predominantly stoichiometrically burning engines is particularly in focus here, since higher temperatures generally prevail here than in a lean-burning engine. In this respect, materials are desired that can withstand the sometimes very high and rapidly changing hydrothermal conditions for as long as possible.
  • the exhaust gas composition is also different compared to lean-burn engine exhaust.
  • concentration, in particular of hydrocarbons and carbon monoxide, which arrive at the catalyst according to the invention is, on the one hand, higher than in lean-burn engines and the composition also changes depending on the driving style around the stoichiometric range (rich/lean change).
  • the hydrothermal temperature stability of zeolites and zeotypes is therefore particularly in demand.
  • the small-pore zeolites used preferably have a SAR value (silica-to-alumina ratio) or the zeotypes have a ratio corresponding to this value of >15 to ⁇ 45, very preferably of >20 to ⁇ 35. Extremely preferred is a Range from 20 – 30 in this context.
  • the large-pore zeolites used preferably have a SAR value (silica-to-alumina ratio) or the zeotypes have a ratio corresponding to this value of >10 to ⁇ 50, very preferably from >10 to ⁇ 40. Extremely preferred is a range of 10 – 30 in this context.
  • SAR value silicon-to-alumina ratio
  • the amount of silicon atoms remaining in the framework is compared to the substitution atoms (Al ions). This results in the number of negative charges in the base body and thus a measure of the number of counterions to be absorbed until electroneutrality is achieved.
  • a corresponding ratio can be determined for Zeotype.
  • the zeolite or zeotype used is ion-exchanged with transition metal ions.
  • the latter are preferably selected from the group consisting of iron and/or copper. Iron is particularly preferred because it has a less oxidizing effect on ammonia compared to copper. These compounds have the possibility of comproportioning nitrogen oxides present in the exhaust gas and the stored ammonia into nitrogen when lean.
  • the zeolite or zeotype described acts as a catalyst for selective catalytic reduction (SCR) (see WO2008106518A2, WO2017187344A1, US2015290632AA, US2015231617AA, WO2014062949A1, US2015231617AA).
  • SCR capability is understood to mean the ability to selectively convert NOx and NH3 in the lean exhaust gas into nitrogen.
  • the metals such as iron and/or copper, which advantageously occur in the catalyst to reduce ammonia emissions, are present in a certain proportion in the first component. This is 0.4-10, more preferably 0.8-7 and most preferably 1.5-5.0% by weight of the first component.
  • the iron and/or copper to aluminum ratio is between 0.05 - 0.8, preferably between 0.2 - 0.5 and most preferably between 0.3 - 0.5 for zeolites. For the zeotype one applies appropriate ratio for the exchange places available there.
  • the metals are at least partially present in ion-exchanged form in the zeolites or zeotypes.
  • ion-exchanged zeolites or zeotypes are already introduced into the first component.
  • the zeolites or zeotypes are brought together with, for example, a binder and a solution of the metal ions in a liquid, preferably water, and then dried (preferably by spraying).
  • a binder preferably a solution of the metal ions in a liquid, preferably water
  • certain proportions of the metals can also be found on the binder in the form of oxides. Both approaches are possible.
  • the first component it is also possible for the first component to contain noble metal, in particular palladium.
  • the first component can preferably have other non-catalytically active components, such as binders.
  • Suitable binders are, for example, non-catalytically active or only slightly catalytically active, temperature-stable metal oxides, such as SiO 2 , Al 2 O 3 and ZrO 2 . The expert knows which materials come into question here.
  • the proportion of such binders in the first coating can, for example, be up to 15% by weight, preferably up to 10% by weight, of the coating.
  • the binder can also contain the above-mentioned transition metals, in particular iron and/or copper. Binders are suitable for ensuring stronger adhesion of the coating to a carrier or another coating. For this purpose, a certain particle size of the metal oxides in the binder is advantageous. This can be adjusted accordingly by a specialist.
  • the ammonia storage ability or capacity addressed in the context of this invention is given as a quotient of the stored mass of ammonia per liter of catalyst support volume.
  • the first component should increase the ammonia storage capacity of the exhaust gas purification system to at least 0.25 g of ammonia per L of carrier volume (measured in the fresh state).
  • the storage capacity of the ammonia storage components used in the form of zeolites or zeotypes should be sufficient to ensure that the system contains between 0.25 and 10.0 g of NH3 per liter of carrier volume, preferably between 0.5 and 8.0 g of NH3 per liter Liter carrier volume and particularly preferably between 0.5 and 5.0 g NH3/liter carrier volume ammonia stored (always based on the fresh condition).
  • the zeolites or zeotypes are present in a sufficient amount in the catalyst to reduce ammonia emissions. The determination of the ammonia storage capacity is shown further below.
  • the second component consists of an OSC-free precious metal catalyst and/or an OSC-containing noble metal catalyst.
  • the second component can optionally also have the binders shown above for the first component.
  • Precious metal refers in particular to the platinum group metals platinum, palladium and rhodium.
  • the noble metals in the OSC-free or OSC-containing noble metal catalyst are preferably selected from the group consisting of palladium, platinum, rhodium.
  • OSC means Oxygen Storage Component.
  • An OSC-containing noble metal catalyst therefore has oxygen storage materials.
  • the OSC-free precious metal catalyst on the other hand, essentially has no function of storing oxygen in the exhaust gas of the internal combustion engine.
  • this component has oxygen storage materials, in particular cerium-zirconium mixed oxides, of less than 10 g/L, preferably less than 5 g/L and most preferably less than 2 g/L carrier volume.
  • Corresponding OSC-free precious metal catalysts have the ability to have an oxidative effect on the substances present (NH 3 , HC, CO) in the already slightly lean exhaust gas of a predominantly stoichiometrically operated combustion engine. This component is preferably designed so that it becomes active at correspondingly low temperatures.
  • the ammonia stored in the zeolite or zeotype is preferably converted into non-harmful nitrogen via this component.
  • the oxidation effect should not be too great, otherwise a certain proportion of the powerful greenhouse gas N2O will be formed from ammonia oxidation.
  • the second component in the form of an OSC-free precious metal catalyst therefore contains materials that have an oxidative effect on, among other things, ammonia. Normally, this component contains a temperature-stable, high-surface metal oxide and at least one noble metal selected from the group rhodium, platinum and palladium.
  • the total precious metal content of this component is preferably from 0.015 - 5 g/L, more preferably from 0.035 - 1.8 g/L and particularly preferably from 0.07 - 1.2 g/L Carrier volume.
  • the precious metals platinum or palladium, or platinum and palladium together, are particularly suitable for use in this component that has an oxidative effect on ammonia.
  • the person skilled in the art can preferably choose whether to use the strongly oxidative platinum alone or, if necessary, in conjunction with palladium in the second coating layer. If platinum and/or palladium is used, the former should be in the range of 0.015 - 1.42 g/L, more preferably 0.035 - 0.35 g/L carrier volume in the coating.
  • palladium When present in the coating, palladium can be present in between 0.015 - 1.42 g/L, preferably 0.035 - 0.35 g/L carrier volume.
  • the weight ratio of platinum to palladium should be between 1:0 and 1:5, more preferably 1:0 and 1:4 and most preferably 1:0 and 1:2.
  • the precious metals in the OSC-free second component are fixed on one or more temperature-stable, high-surface metal oxides as carrier materials. All materials familiar to those skilled in the art for this purpose can be considered as carrier materials. Such materials are in particular metal oxides with a BET surface area of 30 to 250 m 2 /g, preferably 100 to 200 m 2 /g (determined according to DIN 66132 - latest version on the filing date).
  • Particularly suitable carrier materials for the precious metals are selected from the series consisting of aluminum oxide, doped aluminum oxide, silicon oxide, titanium dioxide and mixed oxides from one or more of these.
  • Doped aluminum oxides are, for example, lanthanum oxide, zirconium oxide, barium oxide and/or titanium oxide-doped aluminum oxides.
  • Aluminum oxide or lanthanum-stabilized aluminum oxide is advantageously used, in the latter case lanthanum in amounts of in particular 1 to 10% by weight, preferably 3 to 6% by weight, in each case calculated as La 2 O 3 and based on that Weight of stabilized aluminum oxide is used.
  • the proportion of barium oxide is in particular 1 to 10% by weight, preferably 3 to 6% by weight, in each case calculated as BaO and based on the weight of the stabilized aluminum oxide.
  • Another suitable carrier material is lanthanum-stabilized aluminum oxide, the surface of which is coated with lanthanum oxide, barium oxide and/or strontium oxide.
  • This component preferably comprises at least one aluminum oxide or doped aluminum oxide.
  • La-stabilized aluminum oxide with a surface area of 100 to 200 m 2 /g is particularly advantageous in this context.
  • Such active aluminum oxide is widely described in the literature and is available on the market.
  • the catalyst for reducing ammonia emissions has an OSC-containing catalyst as an alternative or cumulative to the OSC-free noble metal catalyst Precious metal catalyst.
  • an OSC-containing catalyst is also present in the precious metal catalyst (containing OSC). Cerium or cerium-zirconium mixed oxides (see below) are consistently used as oxygen storage materials. Accordingly, an OSC-containing noble metal catalyst is characterized by the presence of a certain amount of these oxygen storage materials. In particular, this component has oxygen storage materials in an amount of more than 10 g/L, preferably more than 15 g/L and most preferably more than 20 g/L carrier volume.
  • the entire cerium-zirconium mixed oxide with all its components is included.
  • Corresponding OSC-containing precious metal catalysts have the ability to have an oxidative effect on the substances present (NH 3 , HC, CO) in the already slightly rich exhaust gas of a predominantly stoichiometrically operated combustion engine.
  • This component is preferably designed so that it becomes active at correspondingly low temperatures.
  • the ammonia stored in the zeolite or zeotype is preferably converted into non-harmful nitrogen via this component.
  • the oxidation effect should not be too great, otherwise a certain proportion of the powerful greenhouse gas N 2 O will be formed from ammonia oxidation.
  • the noble metals in the OSC-containing noble metal catalyst are preferably selected from the group consisting of palladium or rhodium or platinum, platinum and rhodium, palladium and rhodium or palladium and rhodium and platinum together.
  • This catalyst is preferably a coating equipped with three-way catalytic capability.
  • the noble metals can only be deposited on the temperature-stable, high-surface support materials. However, it is preferred if the noble metals are deposited both on the support materials mentioned and on the oxygen storage materials.
  • rhodium is present in this component (whether alone or in combination with the other aforementioned precious metals), this should preferably be in the range of 0.035 - 1.0 g/L, more preferably 0.1 - 0.35 g/L.
  • L carrier volume is located in the respective component. If palladium and/or platinum are also present in this component, those mentioned above apply to the OSC-free precious metal catalysts areas for these metals. Suitable three-way catalytically active coatings are described, for example, in DE102013210270A1, DE102020101876A1, EP3247493A1, EP3727655A1. Modern gasoline engines are operated under conditions with a discontinuous course of the air ratio ⁇ .
  • oxygen storage materials contained in the catalytic converter compensate for these deviations to a certain extent by absorbing oxygen from the exhaust gas as required or released into the exhaust gas (Catalytic Air Pollution Control, Commercial Technology, R. Heck et al., 1995, p.90).
  • OSC-containing noble metal catalysts (such as modern three-way catalysts) therefore contain oxygen storage materials, in particular cerium or Ce/Zr mixed oxides. The mass ratio of cerium oxide to zirconium oxide can vary within wide limits in these mixed oxides.
  • cerium/zirconium mixed oxides include one or more rare earth metal oxides and can therefore be referred to as cerium/zirconium/rare earth metal mixed oxides.
  • cerium/zirconium mixed oxides that do not contain any rare earth metal oxide.
  • the term rare earth metal or rare earth metal oxide in the sense of the present invention does not include cerium or cerium oxide.
  • Rare earth metal oxides in the cerium/zirconium/rare earth metal mixed oxides include, for example, lanthanum oxide, yttrium oxide, praseodymium oxide, neodymium oxide and/or samarium oxide. Lanthanum oxide, yttrium oxide and/or praseodymium oxide are preferred.
  • rare earth metal oxides are lanthanum oxide and/or yttrium oxide and very particularly preferred is the joint presence of lanthanum oxide and yttrium oxide, yttrium oxide and praseodymium oxide, as well as lanthanum oxide and praseodymium oxide in the cerium/zirconium/rare earth metal mixed oxide.
  • this noble metal catalyst has two different cerium/zirconium/rare earth metal mixed oxides, preferably one doped with La and Y and one doped with La and Pr.
  • the oxygen storage components are preferably free of neodymium oxide.
  • the proportion of rare earth metal oxide(s) in the cerium/zirconium/rare earth metal mixed oxides is advantageously 3 to 20% by weight based on the cerium/zirconium/rare earth metal mixed oxide. If the cerium/zirconium/rare earth metal mixed oxides contain yttrium oxide as the rare earth metal, its proportion is preferably 4 to 15% by weight based on the cerium/zirconium/rare earth metal mixed oxide. If the cerium/zirconium/rare earth mixed oxides contain praseodymium oxide as the rare earth metal, its proportion is preferably 2 to 10% by weight based on the cerium/zirconium/rare earth mixed oxide.
  • cerium/zirconium/rare earth metal mixed oxides contain lanthanum oxide and another rare earth oxide as the rare earth metal, such as yttrium oxide or praseodymium oxide, their mass ratio is in particular 0.1 to 1.25, preferably 0.1 to 1.
  • This noble metal catalyst usually contains oxygen storage materials in amounts of 15 to 120 g/l, based on the volume of the carrier or substrate.
  • the OSC-containing noble metal catalysts also have the temperature-stable, high-surface support materials mentioned for the OSC-free noble metal catalysts and, in addition to these, oxygen-storing materials.
  • the mass ratio of temperature-stable, high-surface support materials and oxygen storage components in this component is usually 0.25 to 1.5, for example 0.3 to 1.3.
  • the weight ratio of the sum of the masses of all support materials, such as aluminum oxides (including doped aluminum oxides) to the sum of the masses of all cerium/zirconium mixed oxides in the OSC-containing noble metal catalyst is 10:90 to 75:25, preferably 20:80 to 65:35.
  • the first and second components preferably form an ammonia storage and a function for oxidizing ammonia to nitrogen (eg as in WO2008106523A2). If there are not enough nitrogen oxides in the system to oxidize the stored ammonia, the ammonia can also be converted into nitrogen using the second component with the oxygen present. In both cases, if possible, no ammonia or N2O is released into the environment.
  • the first component and the second component of the catalyst for reducing ammonia emissions can therefore preferably consist of an ammonia-storing coating paired with a second coating that has an oxidative effect on ammonia.
  • they are present in separate coatings one above the other on the substrate. It is particularly preferred if both coatings are of the same length.
  • the OSC-containing noble metal catalyst of component two is located as a top layer over the first component made of zeolites and / or zeotypes for storing ammonia as a bottom layer. Most preferably, no further layers are present below or above these two coatings on the substrate, with the exception of the inert layer.
  • the present exhaust system has a first three-way catalyst and a catalyst positioned downstream to reduce ammonia emissions.
  • the first three-way catalyst can have the same components as the OSC-containing noble metal catalyst of the second component. It is preferably constructed as described in DE102013210270A1, DE102020101876A1, EP3247493A1, EP3727655A1, preferably as described in EP3247493A1.
  • Downstream refers to the fact that the exhaust gas flow first hits the upstream catalytic converter and then the downstream catalytic converter. The reverse applies to the upstream side.
  • Euro 7 legislation it has proven to be advantageous if an exhaust system for a predominantly stoichiometric engine has a unit for filtering small soot and ash particles.
  • GPF are gasoline particle filters and are well known to those skilled in the art (EP3737491A1, EP3601755A1).
  • An exhaust gas design in which the first three-way catalytic converter and the GPF are installed in a position close to the engine is particularly preferred. Close to the engine in the sense of the invention refers to an area in the exhaust system that is in a position close to the engine, i.e. approx. 10 - 80 cm, preferably 20 - 60 cm away from the engine outlet.
  • the catalytic converter is installed last in the exhaust direction in the underbody of a vehicle to reduce ammonia emissions, so that the exhaust gas is then released into the ambient air.
  • the exhaust system can also have additional exhaust units such as additional three-way catalytic converters or hydrocarbon storage (HC traps) or nitrogen oxide storage (LNT).
  • the underbody is the area below the driver's cab.
  • TWC three-way catalytic converter
  • This three-way catalyst is preferably one as described in the prior art (DE102013210270A1, DE102020101876A1, EP3247493A1, EP3727655A1). Zoned or layered versions are now the norm for TWCs.
  • at least one of the additional catalysts with three-way activity has a 2-layer structure with two different three-way coatings, preferably as described in EP3247493A1.
  • the at least second three-way catalytic converter just described in the exhaust system according to the invention can be installed in the underbody of the vehicle, but it can also be in a position close to the engine.
  • the range of possible Euro 7 systems is large.
  • the catalyst for reducing ammonia emissions is preferably located last in the underbody and in fluid communication with the further catalyst or catalysts or the filter of the car exhaust system.
  • the car exhaust system preferably has no additional injection device for ammonia or a precursor compound for ammonia.
  • the present invention relates to a method for reducing harmful exhaust gas components from predominantly stoichiometrically operated internal combustion engines, in particular spark-ignited gasoline engines, in which the exhaust gas is directed via an exhaust system according to the invention. It should be noted that the preferred embodiments of the car exhaust system also apply mutatis mutandis to the present method.
  • the present invention is directed to an exhaust gas purification system, in particular for stoichiometrically operated internal combustion engines.
  • Fig.1 Chart to explain the measurement of ammonia storage capacity.
  • Fig.2 Catalyst for reducing ammonia emissions (1), coating with metal-free zeolites or zeotypes for storing ammonia (2) and a coating with an OSC-free noble metal catalyst and/or an OSC-containing noble metal catalyst (3) and inert layer (4).
  • Fig.3 Schematic representation of the catalysts tested in the underbody position.
  • Fig.4 Comparison of emission values for catalysts with and without an inert layer.
  • Fig.5 Exhaust system according to the invention with a three-way catalytic converter close to the engine (A), GPF close to the engine (B) and the following catalytic converter to reduce ammonia emissions (C).
  • A. Determination of the ammonia storage capacity This is determined experimentally in a flow tube reactor. To avoid undesirable ammonia oxidation on the reactor material, a reactor made of quartz glass is used. A drill core is taken as a test specimen from the area of the catalytic converter whose ammonia storage capacity is to be determined. A drill core with a diameter of 1 inch and a length of 3 inches is preferably taken as a test specimen. The drill core is inserted into the flow tube reactor and at a temperature of 600 ° C in a gas atmosphere consisting of 500 ppm nitrogen monoxide, 5 vol.% oxygen, 5 vol.% water and the rest nitrogen with a space velocity of 30000 h -1 for 10 minutes conditioned.
  • the measuring temperature of 200 °C is then reached in a gas mixture of 0 vol.% oxygen, 5 vol.% water and the rest nitrogen at a space velocity of 30,000 h -1 .
  • the NH 3 storage phase is initiated by switching on a gas mixture of 450 ppm ammonia, 0 vol.% oxygen, 5 vol.% water and the rest nitrogen at a space velocity of 30,000 h -1 .
  • This gas mixture remains switched on until a stationary ammonia breakthrough concentration is recorded on the downstream side of the test specimen.
  • the mass of ammonia stored on the test specimen is calculated from the recorded ammonia breakthrough curve by integration from the start of the NH 3 storage phase until stationarity is reached, taking into account the measured stationary NH 3 breakthrough concentration and the known volume flow (hatched area in Figure 1).
  • the ammonia storage capacity is calculated as the quotient of the stored mass of ammonia divided by the volume of the tested core.
  • Production of the ammonia-storing SCR layers Production of the iron-containing SCR coating
  • the production of the iron-containing zeolite coating was carried out using a washcoat consisting of a zeolite of the BEA structural type, iron (III) nitrate solution and a suitable amount of a binder system made of an Al2O3 and an SiO2 component, with a palladium concentration of 0.706 g/L (20 g/ft 3 ) in the SCR layer being adjusted by adding Pd(NO3)2 solution to the washcoat.
  • the Coating with the desired washcoat amount of 222 g/L was carried out in two steps over 100% of the substrate length.
  • the coated catalyst thus obtained was dried at 90 °C and then calcined at 350 °C for 15 min and annealed in air at 550 °C for 2 h.
  • Aluminum oxide stabilized with lanthanum oxide was suspended in water and, after stirring for one hour, ground twice using circular grinding and once using linear grinding. The suspension thus obtained was used directly to coat a commercially available substrate, with the coating taking place over 100% of the substrate length. The total loading of this washcoat on the catalyst was 50 g/L.
  • the coated catalyst thus obtained was dried at 90 °C and then calcined at 350 °C for 15 min and annealed in air at 550 °C for 2 h.
  • Aluminum oxide stabilized with lanthana oxide was prepared together with an oxygen storage component containing 24 wt.% cerium oxide, 60 wt.% zirconium oxide, 3.5 wt.% lanthanum oxide and 12.5 wt. % yttrium oxide, and lanthanum acetate suspended in water as an additional source of lanthanum oxide.
  • the weight ratio of aluminum oxide to oxygen storage component to additional lanthanum oxide was 43.6:55.7:0.7.
  • a rhodium nitrate solution was then added to the suspension thus obtained with constant stirring.
  • the resulting coating suspension was used directly to coat a commercially available substrate, with the coating taking place over 100% of the substrate length.
  • the aging period and the inlet temperature for the catalytic converter in the underbody position are specified individually for each test.
  • Test conditions The different catalytic converters were tested in the underbody position on a highly dynamic engine test bench in a WLTC driving cycle. Here, a series-produced TWC containing Pd/Rh was placed in an aged state in a position close to the engine.
  • the value “reduction in NH 3 emissions” refers to the NH 3 emissions of a system with one of the catalytic converters shown in the underbody position over the entire driving cycle in relation to the emissions of the corresponding system in the absence of a catalytic converter in underbody position.

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  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
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  • Catalysts (AREA)
  • Exhaust Gas Treatment By Means Of Catalyst (AREA)

Abstract

La présente invention concerne un système de gaz d'échappement destiné à réduire les émissions de gaz d'échappement et en particulier les émissions d'ammoniac dans le train de gaz d'échappement d'un moteur à allumage commandé fonctionnant principalement de manière stœchiométrique.
PCT/EP2023/059087 2022-04-11 2023-04-06 Système de gaz d'échappement pour moteurs à combustion interne fonctionnant principalement de manière stœchiométrique, comprenant un catalyseur pour réduire les émissions d'ammoniac WO2023198577A1 (fr)

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Application Number Priority Date Filing Date Title
DE102022108768.9 2022-04-11
DE102022108768 2022-04-11
DE102022119441.8 2022-08-03
DE102022119441 2022-08-03
DE102022119442.6 2022-08-03
DE102022119443 2022-08-03
DE102022119443.4 2022-08-03
DE102022119442 2022-08-03
DE102023101768.3 2023-01-25
DE102023101779.9 2023-01-25
DE102023101768.3A DE102023101768A1 (de) 2022-04-11 2023-01-25 Abgassystem für überwiegend stöchiometrisch betriebene Verbrennungsmotoren aufweisend einen Katalysator zur Verminderung der Ammoniakemissionen
DE102023101772.1A DE102023101772A1 (de) 2022-04-11 2023-01-25 Abgassystem für überwiegend stöchiometrisch betriebene Verbrennungsmotoren aufweisend einen Katalysator zur Verminderung der Ammoniakemissionen
DE102023101763.2 2023-01-25
DE102023101772.1 2023-01-25
DE102023101763.2A DE102023101763A1 (de) 2022-04-11 2023-01-25 Abgassystem für überwiegend stöchiometrisch betriebene Verbrennungsmotoren aufweisend einen Katalysator zur Verminderung der Ammoniakemissionen
DE102023101779.9A DE102023101779A1 (de) 2022-04-11 2023-01-25 Abgassystem für überwiegend stöchiometrisch betriebene Verbrennungsmotoren aufweisend einen Katalysator zur Verminderung der Ammoniakemissionen

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PCT/EP2023/059078 WO2023198569A1 (fr) 2022-04-11 2023-04-06 Catalyseur de blocage d'ammoniac pour moteurs à combustion interne stoechiométrique
PCT/EP2023/059083 WO2023198574A1 (fr) 2022-04-11 2023-04-06 Système de gaz d'échappement pour moteurs à combustion interne principalement à fonctionnement stœchiométrique, comprenant un catalyseur pour réduire les émissions d'ammoniac
PCT/EP2023/059080 WO2023198571A1 (fr) 2022-04-11 2023-04-06 Système de gaz d'échappement pour moteurs à combustion interne à fonctionnement principalement stœchiométrique, comprenant un catalyseur pour réduire les émissions d'ammoniac
PCT/EP2023/059084 WO2023198575A1 (fr) 2022-04-11 2023-04-06 Système de gaz d'échappement pour moteurs à combustion interne à fonctionnement principalement stœchiométrique, comprenant un catalyseur pour réduire les émissions d'ammoniac
PCT/EP2023/059087 WO2023198577A1 (fr) 2022-04-11 2023-04-06 Système de gaz d'échappement pour moteurs à combustion interne fonctionnant principalement de manière stœchiométrique, comprenant un catalyseur pour réduire les émissions d'ammoniac
PCT/EP2023/059081 WO2023198572A1 (fr) 2022-04-11 2023-04-06 Système de gaz d'échappement pour moteurs à combustion interne principalement à fonctionnement stoechiométrique, comprenant un catalyseur pour réduire les émissions d'ammoniac
PCT/EP2023/059082 WO2023198573A1 (fr) 2022-04-11 2023-04-06 Système de gaz d'échappement pour moteurs à combustion interne à fonctionnement principalement stœchiométrique, comprenant un catalyseur pour réduire les émissions d'ammoniac
PCT/EP2023/059079 WO2023198570A1 (fr) 2022-04-11 2023-04-06 Système de gaz d'échappement pour moteurs à allumage par étincelle fonctionnant principalement de manière stœchiométrique, comprenant un catalyseur permettant de réduire les émissions d'ammoniac

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PCT/EP2023/059078 WO2023198569A1 (fr) 2022-04-11 2023-04-06 Catalyseur de blocage d'ammoniac pour moteurs à combustion interne stoechiométrique
PCT/EP2023/059083 WO2023198574A1 (fr) 2022-04-11 2023-04-06 Système de gaz d'échappement pour moteurs à combustion interne principalement à fonctionnement stœchiométrique, comprenant un catalyseur pour réduire les émissions d'ammoniac
PCT/EP2023/059080 WO2023198571A1 (fr) 2022-04-11 2023-04-06 Système de gaz d'échappement pour moteurs à combustion interne à fonctionnement principalement stœchiométrique, comprenant un catalyseur pour réduire les émissions d'ammoniac
PCT/EP2023/059084 WO2023198575A1 (fr) 2022-04-11 2023-04-06 Système de gaz d'échappement pour moteurs à combustion interne à fonctionnement principalement stœchiométrique, comprenant un catalyseur pour réduire les émissions d'ammoniac

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PCT/EP2023/059082 WO2023198573A1 (fr) 2022-04-11 2023-04-06 Système de gaz d'échappement pour moteurs à combustion interne à fonctionnement principalement stœchiométrique, comprenant un catalyseur pour réduire les émissions d'ammoniac
PCT/EP2023/059079 WO2023198570A1 (fr) 2022-04-11 2023-04-06 Système de gaz d'échappement pour moteurs à allumage par étincelle fonctionnant principalement de manière stœchiométrique, comprenant un catalyseur permettant de réduire les émissions d'ammoniac

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WO2023198573A1 (fr) 2023-10-19
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WO2023198572A1 (fr) 2023-10-19

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