 selective catalytic reduction catalyst system
专利摘要:
abstract catalytic system of selective catalytic reduction scr catalyst systems comprising a first scr catalyst composition and a second scr catalyst composition arranged in the system, the first scr catalyst composition promoting higher n 2 formation and lower n 2 formation than second scr catalyst composition, and the second scr catalyst composition having a different composition from the first scr catalyst composition, the second scr catalyst composition promoting lower n2 formation and greater n2o formation than the first scr catalyst composition . scr catalyst systems are useful in methods and systems for catalyzing the reduction of nitrogen oxides in the presence of a reducer. 1/1 公开号:BR112015022271A2 申请号:R112015022271 申请日:2014-03-13 公开日:2019-09-10 发明作者:L Mohanan Jaya；Tang Weiyong 申请人:Basf Corp； IPC主号:
专利说明:
SELECTIVE CATALYTIC REDUCTION CATALYST SYSTEM TECHNICAL FIELD [0001] The present invention relates to the field of selective catalytic reduction catalysts. More particularly, the embodiments of the invention relate to selective catalytic reduction catalyst systems which comprise a first SCR catalyst composition and a second SCR catalyst composition, a poorly combustion engine exhaust system, and methods of using these. catalyst systems in a variety of processes such as reducing pollutants in exhaust gases. BACKGROUND OF THE INVENTION [0002] The operation of lean mix engines, for example, diesel engines and lean mix gasoline engines, provide the user with excellent fuel economy and have relatively low gaseous hydrocarbon and carbon monoxide emissions due to its operation at high air / fuel rates in poor fuel conditions. Diesel engines, in particular, also offer significant advantages over gasoline engines in terms of durability and their ability to generate high torque at low speed. [0003] From an emissions point of view, however, diesel engines have more serious problems than their spark ignition counterparts. Emission problems concern particulate matter (PM), nitrogen oxides (NO X ), unburned hydrocarbons (HC) and carbon monoxide (CO). NO X is a term used to describe several chemical species of nitrogen oxides, nitrogen monoxide (NO), and nitrogen dioxide (NO 2 ), among others. NO is a concern because it is believed that it participates under a process known as photochemical smog formation, through a series of reactions in the presence of sunlight and hydrocarbons, and NO is a 2/39 significant contributor to acid rain NO 2 , on the other hand, has a high potential as an oxidizer and an oxidizer and is a strong irritant to the lung. Particulate matter (PM) is also linked to respiratory problems. As engine operation changes are made to reduce particulates and unburned hydrocarbons in diesel engines, NO and NO 2 emissions tend to increase. [0004] The effective reduction of NO X in lean mix engines is difficult to achieve, because high conversion rates of NO X typically convert rates requiring conditions rich in reducers. The conversion of the NO X component from exhaust streams into harmless components generally requires specialized NO X decrease strategies for operation in poor fuel conditions. [0005] Selective catalytic reduction (SCR), which uses ammonia or ammonia precursor as a reducing agent, is believed to be the most viable technique for removing exhaust nitrogen oxides from diesel vehicles. In the typical exhaust, nitrogen oxides are mainly composed of NO (> 90%), so that the SCR catalyst favors the conversion of NO and NH 3 into nitrogen and water. The two main challenges in the development of catalysts for the automotive application of the ammonia SCR process are to provide a wide operating window for SCR activity, including low temperatures from 200 ° C and higher and improving hydrothermal stability of the catalyst for temperatures above 500 ° C. As used in this document, hydrothermal stability refers to the retention of a material's ability to catalyze the NO X SCR, with a preference that the retention is at least 85% of the material's NO X conversion ability prior to hydrothermal aging. . 3/39 [0006] Metal-promoted zeolite catalysts including, but not limited to, iron-promoted and copper-promoted zeolite catalysts, where, for example, metal is introduced via ion exchange, for the selective catalytic reduction of oxides nitrogen with ammonia are known. Iron-promoted beta zeolite has been an effective catalyst for the selective reduction of nitrogen oxides with ammonia. Unfortunately, it was found that the same under harsh hydrothermal conditions, such as, for example, the reduction of NO X from gas escaping at temperatures exceeding 500 ° C, the activity of many zeolites promoted by metal, such as, for example, Cu and Fe versions of ZSM-5 and Beta, begins to decline. This decline in activity is believed to be due to the destabilization of the zeolite, for example, through dealumination and the consequent loss of catalytic sites containing metal within the zeolite. [0007] In order to maintain the general NO X reduction activity, the marked levels of the coating coating by immersion of the zeolite catalyst promoted by iron need to be provided. As zeolite catalyst levels are increased to provide adequate NO X removal, there is an obvious reduction in the cost efficiency of the process for removing NO X as the catalyst costs increase. [0008] In some SCR systems, in particular, heavy duty diesel engine (HDD), which control the secondary N 2 O pollutant emitted from the SCR system has become more important. In addition, certain existing catalysts, such as promoted copper zeolites (for example, Cu-SSZ-13), tend to produce an unacceptably high level of N 2 O emissions. Due to the fact that N 2 O is a greenhouse effect and emissions regulations are becoming increasingly strict, there is a need for systems that reduce the amount of N 2 O emitted from SCR systems. 4/39 SUMMARY [0009] One aspect of the invention concerns a selective catalytic reduction (SCR) catalyst system. In a first embodiment, the system comprises a first SCR catalyst composition and a second SCR catalyst composition positioned in the system, the first SCR catalyst composition promoting greater N 2 formation and less N 2 O formation than the second SCR catalyst composition, and the second SCR catalyst composition having a different composition than the first SCR catalyst composition, the second SCR catalyst composition promoting less N 2 formation and greater N 2 O formation than the first SCR catalyst composition. [0010] In a second embodiment, the first SCR catalyst composition is modified so that the first SCR catalyst composition and the second SCR catalyst composition are positioned on a common substrate. [0011] In a third embodiment, the SCR catalyst system of the first or second embodiment is modified so that the first composition of the SCR catalyst is located upstream of the second composition of the SCR catalyst. [0012] In a fourth embodiment, the SCR catalyst system from the first to the third embodiments is modified so that the first SCR catalyst composition and the second SCR catalyst composition are arranged on different substrates. [0013] In a fifth embodiment, the system of the first to the fourth embodiments is modified so that the first composition of the SCR catalyst is located upstream of the second composition of the SCR catalyst. [0014] In a sixth embodiment, the first or second embodiments are modified in which the first composition of the catalyst 5/39 SCR and the second SCR catalyst composition are in a layered relationship, with the first layered SCR catalyst composition on top of the second SCR catalyst composition. [0015] In the seventh embodiment, any one of the first to the sixth embodiments, the SCR catalyst system of the claim of the first composition of the SCR catalyst comprises a mixed oxide. [0016] In an eighth modality, the seventh modality can be modified so that the mixed oxide is selected from Fe / titanium, Fe / alumina, Mg / titanium, Cu / titanium, Ce / Zr, vanadium / titanium, and mixtures thereof . [0017] In a ninth modality, the eighth modality is modified so that the mixed oxide comprises vanadium / titanium. [0018] In a tenth modality, the ninth modality is modified so that the vanadium / titanium is stabilized with tungsten. [0019] In an eleventh embodiment, any one of the first to the eleventh modalities can be modified in which the second SCR catalyst comprises a small pore ring-exchanged metal-8 molecular sieve. [0020] In an twelfth modality, the eleventh modality can be modified in which the molecular sieve has a type of structure selected from the group consisting of AEI, AFT, AFX, CHA, EAB, HE, KFI, LEV, SAS, SAT , DDR, and SAV. [0021] In a thirteenth modality, the twelfth modality is modified in which the molecular sieve is an aluminosilicate zeolite and has the CHA type structure. [0022] In a fourteenth modality, the thirteenth modality is modified in which the zeolite is selected from SSZ-13 and SSZ-62. 6/39 [0023] In a fifteenth modality, any one from the eleventh to the fourteenth modality can be modified in which the metal is selected from the group consisting of Cu, Fe, Co, Ce and Ni. [0024] In a sixteenth modality, the fifteenth modality is modified, in which the metal is selected from Cu. [0025] In a seventeenth modality, the sixteenth modality is modified, in which the zeolite is exchanged with Cu in the range of 2% to 8% by weight. [0026] An eighteenth modality relates to a selective catalytic reduction catalyst (SCR) system comprising a first catalyst composition comprising SCR vanadium / titanium disposed on a substrate and a second SCR catalyst composition comprising a small pore molecular sieve. rings-8 exchanged with metal disposed on a substrate. [0027] In a nineteenth modality, the eighteenth modality can be modified in which the molecular sieve has a type of structure selected from the group consisting of AEI, AFT, AFX, CHA, EAB, ERI, KFI, LEV, SAS, SAT , DDR, and SAV. [0028] In a twentieth modality, the nineteenth modality is modified in which the molecular sieve is an aluminosilicate zeolite and has the structure of the CHA type. [0029] In a twenty-first modality, the twenty modality is modified in which the zeolite is selected from SSZ-13 and SSZ-62. [0030] In a twenty-second modality, the eighteenth to the twenty-first modality are modified, in which the metal is selected from the group consisting of Cu, Fe, Co, Ce and Ni. [0031] In a twenty-third modality, the twenty-second modality are modified, in which the metal is selected from Cu. 7/39 [0032] In a twenty-fourth modality the eighteenth to the twenty-third modalities are modified, in which the zeolite is exchanged with Cu in the range of 2% to 8% by weight. [0033] In a twenty-fifth modality, the eighteenth to twenty-fourth modality in which vanadium / titanium are modified is stabilized with tungsten. [0034] In a twenty-sixth modality, the eighteenth to the twenty-fifth modalities are modified, in which the first SCR catalyst composition and second SCR catalyst composition are arranged on a common substrate. [0035] In a twenty-seventh modality, the eighteenth to the twenty-sixth modalities are modified, in which the first SCR catalyst composition is located upstream of the second SCR catalyst composition. [0036] In a twenty-eighth modality, the eighteenth to the twenty-seventh modalities are modified, in which vanadium / titanium promotes greater formation of N 2 and less formation of N2O than the molecular sieve of the metal-exchanged small pore-8 pore, and wherein the small pore molecular sieve with metal rings 8permutado-formation promoting formation and lower C 2 N 2 to the upper vanadium / titanium. [0037] In a twenty-ninth modality, the eighteenth to twenty-fifth modalities are modified, in which the first composition of the SCR catalyst and the second composition of the SCR catalyst are arranged on the separate supports. [0038] In a thirty modality, the twenty-ninth modality is modified, in which the first composition of the SCR catalyst is located upstream of the second composition of the SCR catalyst. 8/39 [0039] In a thirty-first modality, the twenty-sixth modality is modified in which the first composition of the catalyst SCR and the second SCR catalyst composition are in a layered relationship, with the first SCR catalyst composition layered on top of the second SCR catalyst composition. [0040] In a thirty-second modality, the thirty-fifth modality is modified, in which the molecular sieve has a type of structure selected from the group consisting of AEI, AFT, AFX, CHA, EAB, ERI, KFI, LEV, SAS, SAT , DDR, and SAV. [0041] In a thirty-third modality, the thirty-second modality is modified, in which the molecular sieve is an aluminosilicate zeolite and has the CHA type structure. [0042] In a thirty-fourth modality, the thirty-third modality is modified, in which the zeolite is selected from SSZ13 and SSZ-62. [0043] In thirty-fifth modality, the thirty-first to the thirty-fourth modalities are modified, in which the metal is selected from the group consisting of Cu, Fe, Co, Ce, and Ni. [0044] In a thirty-sixth modality, the thirty-fifth modality is modified, in which the metal is selected from Cu. [0045] In a thirty-seventh modality, the thirty-third modality is modified, in which the zeolite is exchanged with Cu. [0046] In a thirty-eighth modality, the thirty-first to the thirty-seventh modalities are modified, in which vanadium / titanium is stabilized with tungsten. [0047] Another aspect of the invention relates to a poor exhaust exhaust from the treatment system engine. In a thirty-ninth modality, an exhaust gas treatment system for the low-burn engine comprises the catalytic system of any one of the first to thirty-seventh modalities, a flaring mechanism 9/39 poor, and an exhaust gas duct in fluid communication with the lean-burn engine, where the catalyst system is downstream of the engine. [0048] In a fortieth modality, the thirty-ninth modality is modified, in which the engine is a heavy-duty diesel engine. [0049] Another aspect of the invention concerns a method of removing nitrogen oxides from the exhaust gases of a poorly burning engine. In the forty-first modality, a method of removing nitrogen oxides from the exhaust gases of a lean mix engine, the method comprising contacting an exhaust gas stream with the selective catalytic reduction of the catalyst system (SCR) which includes a first catalyst composition comprising SCR vanadium / titanium arranged on a substrate and a second composition of the SCR catalyst comprising a small pore molecular sieve of the metal-exchanged ring-8 arranged on a substrate. [0050] In a forty-second modality, the forty-first modality is modified, in which the exhaust gas comprises NO X. [0051] In a fortieth modality, the forty-first and fortieth second modalities are modified, in which the poor-burning engine is a heavy-duty diesel engine. [0052] In a forty-fourth modality, an exhaust gas treatment system for the lean burn engine comprises the catalyst system of the nineteenth modality, a poor burn engine, and an exhaust gas duct in fluid communication with the poor-burning engine, where the catalyst system is downstream of the engine. 10/39 [0053] In a forty-fifth modality, the forty-fourth modality is modified, in which the engine is a heavy-duty diesel engine. [0054] A forty-sixth modality refers to a method of removing nitrogen oxides from the exhaust gases of a poorly combustion engine, the method comprising the contact of the exhaust gas with the catalytic reduction of the selective catalyst system (SCR) which includes a first composition of the SCR catalyst and a second composition of the SCR catalyst arranged in the system, the first composition of the SCR catalyst promoting greater N 2 formation and less N 2 formation than the second catalyst composition, and the second catalyst composition which has a different composition than the first SCR catalyst composition, the second catalyst composition promotes less N 2 formation and greater N 2 O formation than the first SCR catalyst composition. [0055] In a forty-seventh modality, the first to the thirty-seventh modalities are modified, in which the second catalyst composition has a greater NH 3 storage capacity than the first catalyst composition. [0056] In a forty-eighth modality, a selective catalytic reduction (SCR) of the hybrid catalyst system for the removal of NOx from the engine exhaust gases, the system comprises a first composition of the SCR catalyst and a second composition of the SCR catalyst arranged in the system, the first SCR catalyst composition having a faster DeNOx response time when exposed to ammonia than the second catalyst composition and the second SCR catalyst composition has a higher steady-state DeNOx performance than the first catalyst composition and the first composition of the SCR catalyst provides a target DeNOx percentage at a lower ammonia storage level than the second 11/39 composition of the SCR catalyst to provide the same percentage DeNOx, and where the system provides higher performance Steady-state DeNOx than the first catalyst composition. [0057] In a forty-ninth modality, the forty-eighth is modified, in which under acceleration conditions in which sudden increases in the exhaust temperature are produced, the ammonia dissolved from the hybrid system due to the temperature increase is less than the ammonia dissolved from a system that has only the second catalyst composition. [0058] In a fiftieth modality, the fortieth eighth or fortieth ninth modalities are modified, in which the first catalyst composition comprises vanadium / titanium oxide stabilized with tungsten. [0059] In the fifty-first embodiment, the fifty-fifth embodiment is modified, in which the second catalyst composition comprises a small pore molecular sieve of the metal-exchanged ring8. [0060] In a fifty-second modality, the fifty-first modality is modified, in which the molecular sieve has a type of structure selected from the group consisting of AEI, AFT, AFX, CHA, EAB, ERI, KFI, LEV, SAS, SAT , DDR, and SAV. [0061] In a fifty-third modality, the fifty-second modality is modified, in which the molecular sieve is an aluminosilicate zeolite and has the CHA type structure. [0062] In a fifty-fourth modality, the forty-eighth to fifty-third modalities are modified, in which the zeolite is selected from SSZ-13 and SSZ-62 and the metal comprises Cu. [0063] In a fifty-fifth modality, the system of the first to thirty-eighth modalities are modified in which the 12/39 first SCR catalyst composition promotes higher N 2 formation and lower N 2 O formation than the second catalyst composition SCR, and the second composition of the SCR catalyst promotes lower N 2 formation and higher N 2 O formation in a temperature range of 200 ° C to 600 ° C. [0064] In the fifty-sixth modality, the forty-eighth to the fifty-fourth modalities are modified, in which the first SCR catalyst composition has a faster DeNOx response time when exposed to ammonia than the second catalyst composition and the second SCR catalyst composition having a higher steady-state DeNOx performance than the first catalyst composition and the first SCR catalyst composition provide a target percentage of DeNOx at a lower ammonia storage level than the second SCR catalyst composition to provide the same percentage of DeNOx, and where the system provides a higher performance of DeNOx at steady state than the first catalyst composition for forming a temperature range of 200 ° C to 600 ° C. BRIEF DESCRIPTION OF THE FIGURES [0065] FIG. 1 shows a cross-sectional view of an SCR catalyst system according to one or more embodiments; [0066] FIG. 2 shows a partial cross-sectional view of an SCR catalyst system according to one or more embodiments; [0067] FIG. 3 shows a cross-sectional view of an SCR catalyst system according to one or more embodiments; [0068] FIG. 4 is a graph comparing N 2 O emissions for an SCR catalyst system according to one or more modalities and a comparative system; 13/39 [0069] FIG. 5 is a graph comparing N 2 O emissions for an SCR catalyst system according to one or more modalities and a comparative system; [0070] FIG. 6 is a graph comparing N 2 O emissions for an SCR catalyst system according to one or more modalities and a comparative system, both systems with an oxidation catalyst upstream of the diesel; [0071] FIG. 8 is a graph comparing the NO x conversions of an SCR catalyst system according to one or more modalities and a comparative system, both systems with an oxidation catalyst upstream of the diesel; [0072] FIG. 9 is a graph comparing NO X conversions after sulfation of an SCR catalyst system according to one or more modalities and a comparative system, both systems with an oxidation catalyst upstream of the diesel; [0073] FIG. 10 is a graph generated by a computer model, as described in Example 6, which shows a Response Curve of the DeNO x vs. vs. Analysis. Time at 225 ° C and 10% NO 2 ; and [0074] FIG. 11 is a graph generated by a computer model, as described in Example 6, showing a DeNO Analysis Response Curve x vs. Total Absorbed NH 3 at 225 ° C and 10% NO 2 . DETAILED DESCRIPTION [0075] Before describing several exemplary embodiments of the invention, it should be understood that the invention is not limited to the details of construction or process steps set out in the following description. The invention is capable of other modalities and can be practiced or performed in different ways. [0076] Government regulations mandate the use of NO X reduction technologies for low-burn engine vehicles 14/39 light and heavy duty. The selective catalytic reduction (SCR) of NO x using urea is an effective and dominant emission control technology for NO x control. To meet future government regulations, an SCR catalyst system that has improved performance compared to current Cu-SSZ-13 systems. The modalities of the invention relate to an SCR catalyst system that has lower N 2 O emissions and also improved efficiency of NO X conversion at low levels of NH 3 storage than simple SCR catalyst systems and other systems of dual SCR catalyst. Without the intention of being linked to the theory, it is believed that the dynamic response of the SCR catalyst system according to one or more modalities is provided through the improved NH 3 storage capacity. The characteristics of the invention described here must be provided over the entire SCR temperature range of interest, that is, 200 ° C to 600 ° C. According to one or more embodiments, the first and second compositions of the SCR catalyst exclude metals from the platinum group, such as Pt, Pd and Rh. [0077] The modalities of the invention are directed to SCR catalyst systems, methods for their preparation, exhaust gas purification systems and exhaust gas nitrogen oxide reduction methods with the use of such SCR catalyst systems. [0078] The modalities are directed to the use of SCR catalyst systems that provide the improved NO X performance for poorly burning engines. While SCR catalyst systems can be used in any low-burn engine, in specific embodiments, catalyst systems must be used in heavy-duty diesel engine applications. Heavy duty diesel engine applications include diesel powered vehicles that have a gross vehicle weight rating (GVWR) of over 8,500 Ibs by the federal government and over 14,000 Ibs in California (model year 1995 15/39 and later). SCR catalyst systems according to the modalities can be used in other engines as well, including, but not limited to, non-road diesel engines, locomotives, marine engines, and stationary diesel engines. The invention may have applicability to other types of low-burn engines as well, for example, light-duty diesel engines, compressed natural gas engines and low-burn gasoline direct injection engines. [0079] With regard to the terms used in the disclosure, the following definitions are provided. [0080] As used in this document, the term catalyst or catalyst composition refers to a material that promotes a reaction. As used herein, the phrase catalyst system refers to a combination of two or more catalysts, for example, a combination of a first SCR catalyst and a second SCR catalyst. The catalyst system can be in the form of an immersion coating in which the two SCR catalysts are mixed. [0081] As used in this document, the terms upstream and downstream refer to relative directions according to the flow of an engine exhaust gas stream from an engine towards an exhaust, with the engine in one upstream and exhaust and any pollution reduction items such as filters and catalysts are downstream of the engine. [0082] As used in this document, the term current refers broadly to any combination of flowing gas that may contain matter in solid or liquid particle. The term gaseous stream or exhaust gas stream means a stream of gaseous constituents such as the exhaust from a poorly burning engine, which may contain entrained non-gaseous components such as liquid droplets, solid particles, and the like. The exhaust gas flow of an engine 16/39 poor burning also typically comprises combustion products, incomplete combustion products, nitrogen oxides, particulate matter in fuel and / or carbonaceous (soot), and unreacted oxygen and nitrogen. [0083] As used in this document, the term substrate refers to monolithic material, on which the catalyst composition is placed, typically in the form of an immersion coating that contains a plurality of particles containing a catalytic composition therein. An immersion coating is formed by preparing a paste that contains a specified solids content (for example, 30-90% by weight) of particles in a liquid carrier, which is then coated on a substrate and dried to provide a layer of dip coating. [0084] As used in this document, the term immersion coating has its common meaning in the technique of a thin and adherent coating of a catalytic material or other material applied to a substrate material, such as a honeycomb carrier member, which it is sufficiently porous to allow the flow of gas being treated to pass through. [0085] Catalytic article refers to an element that is used to promote a desired reaction. For example, a catalytic article can include a dip coating that contains catalytic compositions on a substrate. [0086] In one or more modalities, the substrate is a ceramic or metal that has a honeycomb structure. Any suitable substrate can be employed, such as a monolithic substrate of the type that has parallel slender gas flow passages that extend through it from an entrance face or an exit face of the substrate, so that the passages are open to the fluid flow through them. The passages, which are essentially 17/39 straight paths from the fluid inlet to the fluid outlet are defined by walls in which the catalyst material is coated as an immersion coating so that gases flowing through the passages come into contact with the catalytic material . The flow passages of the monolithic substrate are thin-walled channels, which can have any suitable cross-sectional shape and size, such as trapezoidal, rectangular, square, sinusoidal, hexagonal, oval, circular, etc. Such structures can contain from about 60 to about 900 or more gas inlet openings (i.e., cells) per square inch of cross-section. [0087] The ceramic substrate can be made of any suitable refractory material, for example, cordierite, cordierite-α alumina, silicon nitride, zirconium mullite, spodumene, silica-magnesia alumina, zirconium silicate, sillimanite, a silicate magnesium, zirconium, petalite, aalumina, an aluminosilicate and the like. [0088] The substrates useful for the catalyst compositions of the embodiments of the present invention can also be of a metallic nature and are composed of one or more metals or metal alloys. Metal substrates can be used in various formats, for example, in pellets, corrugated sheet or monolithic form. Specific examples of metallic substrates include heat-resistant base metal alloys, especially those in which iron is a substantial or major component. Such alloys may contain one or more of nickel, chromium, and aluminum, and the total of these metals may advantageously comprise at least about 15% by weight of the alloy, for example, about 10 to 25% by weight of chromium, about 1 to 8% by weight of aluminum, and about 0 to 20% of nickel. [0089] According to a first aspect of the invention, a selective catalytic reduction catalyst (SCR) system comprises a first SCR catalyst composition and a second 18/39 SCR catalyst composition arranged in the system. In one or more embodiments, the second SCR catalyst composition has a different composition than the first SCR catalyst composition. The first composition of the SCR catalyst promotes a higher formation of N 2 and a lower formation of N 2 O than the second composition of SCR catalyst, while the second composition of catalyst promotes a formation of lower N 2 and higher formation of N 2 What the first SCR catalyst composition. To reduce NH 3 emissions, in one or more modalities, the first SCR catalyst must have a lower NH 3 desorption temperature / adsorption capacity than the second SCR catalyst composition. [0090] In one or more embodiments, the first SCR catalyst composition and the second SCR catalyst composition are on the same or on a common substrate. In other embodiments, the first SCR catalyst composition and the second SCR catalyst composition are on separate substrates. [0091] In one embodiment, the first SCR catalyst and the second SCR catalyst are arranged in a laterally zoned configuration, with the first catalyst upstream of the second catalyst. The upstream and downstream catalysts can be arranged on the same substrate or on different substrates separated from each other. In another specific embodiment, the first SCR catalyst and the second SCR catalyst are in a layered arrangement, with the second SCR catalyst being arranged on a substrate and the first SCR catalyst in a layer that covers the second SCR catalyst. Each of these modalities will be described in more detail below. [0092] In specific embodiments, each of the first SCR catalyst composition and the second SCR catalyst composition is used as a molded catalyst, further 19/39 specifically as a molded catalyst in which the SCR catalyst composition is deposited on a suitable refractory substrate, even more specifically on a honeycomb type substrate, for selective reduction of NO X nitrogen oxides, that is, for the selective catalytic reduction of nitrogen oxides. According to the embodiments of the invention, the SCR catalyst composition can be in the form of self-sustaining catalyst particles, or as a honeycomb monolith formed from the SCR catalyst composition. [0093] According to one or more embodiments, the first SCR catalyst composition comprises a mixed oxide. As used in this document, the term mixed oxide refers to an oxide that contains cations from more than one chemical element or cations from a single element in various oxidation states. In one or more embodiments, the mixed oxide is selected from Fe / titanium (eg, FeTiO 3 ), Fe / alumina (eg, FeAI 2 O 3 ), Mg / titanium (eg MgTiO 3 ), Mg / alumina ( for example MgAI 2 O 3 ), Mn / alumina, Mn / titanium (for example MnO x / TiO 2 ) (for example MnO x / AI 2 O 3 ), Cu / titanium (for example CuTiO 3 ), Ce / Zr ( for example, CeZrO 2 ), Ti / Zr (for example, TiZrO 2 ), vanadium / titanium (for example, V 2 O 5 / TiO 2 ), and mixtures thereof. In specific embodiments, the mixed oxide comprises vanadium / titanium. Titanium / vanadium can be activated or stabilized with tungsten (for example, WO 3 ) to provide V 2 O 5 / TiO 2 / WO 3 . [0094] According to one or more modalities, a first SCR catalyst composition comprising vanadium / titanium that generates significantly less N 2 O than SCR catalyst zeolites, especially under rich NO 2 conditions. In one or more embodiments, the first composition of the SCR catalyst comprises titanium over which vanadium has been dispersed. Vanadium can be dispersed in concentrations ranging from 1 to 10% by weight, including 1.2, 3, 4, 5, 6, 7, 8, 9, 10% by weight. In the specific modalities of vanadium it is activated or stabilized by 20/39 tungsten (WO 3 ). Tungsten can be dispersed in concentrations ranging from 0.5 to 10% by weight, including 1.2, 3, 3. 4, 5, 6, 7, 8, 9 and 10,% by weight. All percentages are on an oxide basis. [0095] According to one or more modalities, the second SCR catalyst comprises a metal-exchanged molecular sieve. The metal is selected from Cu, Fe, Co, Ni, Ce and Pt. In the specific modalities, the metal is Cu. [0096] As used in this document, the term molecular sieves refer to materials based on an extensive three-dimensional network of oxygen ions containing locations of the generally tetrahedral type and having a pore distribution. Molecular sieves such as zeolites have been widely used to catalyze a series of chemical reactions in refinery and petrochemical reactions, and catalysis, adsorption, separation and chromatography. For example, with respect to zeolites, both natural and synthetic zeolites and their use in promoting certain reactions, including converting methanol to olefins (MTO reactions) and selective catalytic reduction (SCR) of nitrogen oxides with a reducer such as ammonia, urea or a hydrocarbon in the presence of oxygen, are well known in the art. Zeolites are crystalline materials, having very uniform pore sizes that, depending on the type of zeolite and the type and quantity of cations included in the zeolite structure, vary from about 3 to 10 Angstroms in diameter. [0097] The compositions of the catalysts employed in the SCR process should ideally be able to maintain good catalytic activity over the wide range of temperature conditions of use, for example, 200 ° C to 600 ° C or higher, under hydrothermal conditions. Hydrothermal conditions are often encountered in practice, such as during the regeneration of a soot filter, a component of the exhaust gas treatment system used to remove particles. 21/39 [0098] According to the modalities, the molecular sieves of the second SCR catalyst composition have 8-ring pore openings and double six-ring secondary construction units, for example, those having the following types of structure: AEI , AFT, AFX, CHA, EAB, ERI, KFI, LEV, SAS, SAT, DDR, and SAV. According to one or more modalities, it will be appreciated that when defining molecular sieves by their type of structure, it is intended to include the type of structure and any and all isotypic frame material such as SAPO, AIPO and MeAPO materials, having the same type of structure. [0099] Zeolites having 8-ring pore openings and secondary double six-ring building units, particularly those having cage-like structures have recently found interest in use as SCR catalysts. A specific type of zeolite with these properties is chabazite (CHA), which is a small pore zeolite with eight ring member pore openings (having a pore size of at least a maximum dimension of less than 4.3 Angstroms, for example, about 3.8 Angstrom) accessible through its three-dimensional porosity. A cage-like structure results from the connection of double six-ring building units by 4 rings. [00100] Aluminosilicate zeolites promoted by metal, especially promoted by copper, having the type of structure CHA (for example, SSZ-13 and SSZ-62) and a molar ratio of silica to alumina greater than 1, specifically those having a ratio molar silica to alumina greater than or equal to 5, 10, or 15 and less than about 1000, 500, 250, 100 and 50 have recently aroused a high degree of interest as catalysts for the SCR of nitrogen oxides in mixing engines poor using nitrogen reducers. This is due to the wide temperature window together with the excellent hydrothermal durability of these materials, as described in United States Patent Number 7,601,662. Before the discovery of zeolites promoted by metal 22/39 described in United States patent number 7,601,662, while the literature had indicated that a large number of metal-promoted zeolites had been proposed in the scientific and patent literature for use as SCR catalysts, each of the proposed materials suffered from one or both of the following defects: (1) poor conversion of nitrogen oxides at low temperatures, for example 350 ° C and below; and (2) poor hydrothermal stability, marked by a significant decline in catalytic activity in the conversion of nitrogen oxides by SCR. Thus, the invention described in United States patent number 7,601,662 addressed an imperative, unresolved need to provide a material that would provide the conversion of nitrogen oxides at low temperatures and retention of SCR catalytic activity after hydrothermal aging at temperatures above 650 ° C. [00101] Zeolitic chabazite includes a naturally occurring tectosilicate mineral from a zeolite group with an approximate formula: (Ca, Na 2 , K 2 , Mg) AI 2 Si 4 O 12 · 6H 2 O (eg aluminum silicate of hydrated calcium). Three synthetic forms of zeolitic chabazite are described in Zeolite Molecular Sieves, by DW Breck, published in 1973 by John Wiley & Sons, incorporated by reference. The three synthetic forms reported by Breck are Zeolite KG, described in J. Chem. Soc., P. 2822 (1956), Barrer et al; Zeolite D, described in British Patent No. Q 868,846 (1961); and Zeolite R, described in US Patent No. 3,030,181, which are incorporated herein by reference. The synthesis of another synthetic form of the zeolitic chabazite, SSZ-13, is described in Pat. US N Q 4,544,538, which is incorporated herein by reference. The synthesis of a synthetic form of a molecular sieve having the chabazite crystal structure, silicoaluminophosphate 34 (SAPO-34), is described in EU patent 4,440,871 and n. Q 7,264,789, which are incorporated by reference in this document. One method of making yet another molecular sieve having 23/39 chabazite structure, SAPO-44, is described in U.S. Patent No. 6,162,415, which is incorporated herein by reference. [00102] In the most specific modalities, reference to a type of aluminosilicate zeolite structure limits the material to molecular sieves that do not include phosphorus or other substituted metals in the frame. Obviously, aluminosilicate zeolites can subsequently have an ion exchange with one or more promoting metals such as metals of the group iron, copper, cobalt, nickel, cerium or platinum. However, to make it clear, as used in this document, aluminosilicate zeolite excludes aluminophosphate materials such as SAPO, AIPO and MeAPO materials, and the broader term zeolite is intended to include aluminosilicates and aluminophosphates. In one or more embodiments, the molecular sieve can include all aluminosilicate, borosilicate, galossilicate, MeAPSO, and MeAPO compositions. These include, but are not limited to, SSZ-13, SSZ-62, natural chabazite, zeolite K-G, Linde D, Linde R, LZ-218, LZ-235. LZ-236, ZK-14, SAPO-34, SAPO-44, SAPO-47, ZYT-6, CuSAPO-34, CuSAPO-44, and CuSAPO-47. [00103] In one or more modalities, the molecular sieve of the second composition of the SCR catalyst has a type of structure selected from the group consisting of AEI, AFT, AFX, CHA, EAB, IIE, KFI, LEV, SAS, SAT, DDR, and SAV. In a specific embodiment, the molecular sieve is an aluminosilicate zeolite and has the type of CHA structure, for example, SSZ-13 or SSZ-62. In another specific embodiment, the molecular sieve is an aluminosilicate zeolite and has the structure type AEI, for example SSZ-39. [00104] In the specific embodiments, the small 8-ring pore molecular sieve promoted by copper has a molar ratio of silica to alumina greater than about 15, even more specifically greater than about 20. In the specific embodiments, the molecular sieve of small 8-ring pores promoted by copper has a molar ratio 24/39 silica to alumina in the range of about 20 to about 256, more specifically in the range of about 25 to about 40. [00105] In specific modalities, the atomic ratio of copper to aluminum exceeds about 0.25. In more specific embodiments, the copper to aluminum ratio is about 0.25 to about 1, even more specifically about 0.25 to about 0.5. In even more specific embodiments, the copper to aluminum ratio is about 0.3 to about 0.4. [00106] In general, the SCR catalyst system according to one or more modalities should exhibit as much NO X good temperature conversion activity (NO X > 50% conversion at 200 ° C) and good high temperature conversion activity NO X (NO X conversion> 70% at 450 ° C). NO X activity is measured under stable conditions at maximum NH 3 -slip conditions in a gas mixture of 500 ppm NO, 500 ppm NH 3 , 10% O 2 , 5% H 2 O, equilibrate N 2 at a rate space based on volume of 80000 h ' 1 . [00107] According to one or more modalities, to reduce NH 3 emissions, the first SCR catalyst composition must have a lower NH 3 adsorption / desorption temperature than the second SCR catalyst composition. [00108] According to one or more embodiments, the second composition of the SCR catalyst comprises a metal-exchanged 8-ring small pore molecular sieve. In other words, the second composition of the SCR catalyst is a molecular sieve with small 8-ring pores that is promoted with metal. In one or more modalities, the metal can be selected from the group consisting of Cu, Fe, Co, Ce, and Ni. In a specific modality, the metal is selected from Cu. Metal promoter% by weight: 25/39 [00109] The promoter metal (eg Cu) of the content of the metal-exchanged small pore 8-ring molecular sieve, calculated as metal oxide, in specific embodiments, is at least about 2 -% by weight, even more specifically, at least about 2.5-% by weight and in even the most specific modalities, at least about 3-% by weight, reported on a free volatile basis. In even more specific embodiments, the metal (eg Cu) of the molecular sieve content of the small metal-exchanged 8-ring pore, calculated as metal oxide, is in the range of up to about 8-% by weight, based on the total weight of the calcined molecular sieve reported on a volatile free base. Therefore, in the specific modalities, the range of the 8-ring small pore molecular sieve promoted with a metal selected from Cu, Fe, Co, Ce, and Ni, calculated as the metal oxide, is about 2 to about 8-% by weight, more specifically from about 2 to about 5-% by weight, and even more specifically from about 2.5 to about 3.5-% by weight, in each case reported on a oxide. [00110] In one or more embodiments, the first SCR catalyst and the second SCR catalyst are arranged in a laterally zoned configuration, with the first catalyst upstream of the second catalyst. As used herein, the term laterally zoned refers to the location of the two SCR catalysts relative to each other. Lateral means side-by-side so that the first SCR catalyst composition and the second SCR catalyst composition are located side by side with the first SCR catalyst composition upstream of the second SCR catalyst composition. According to one or more embodiments, the first and second laterally zoned SCR catalysts can be arranged on the same or on a common substrate or on different substrates separated from each other. 26/39 [00111] According to one or more modalities, ο vanadium / titanium and the metal-exchanged 8-ring small pore molecular sieve are arranged in common with one or the same substrate. In other embodiments, vanadium / titanium and the metal-exchanged 8-ring small pore molecular sieve are arranged on separate supports. Whether on the same substrate or on different supports, according to one or more modalities, the vanadium / titanium is located in the small metal-exchanged 8-ring molecular sieve. [00112] In one or more modalities, vanadium / titanium promotes higher N 2 formation and lower N 2 O formation than the metal-exchanged 8-ring small pore molecular sieve and the small pore molecular sieve of Metal-exchanged 8-rings promote lower N 2 formation and higher N 2 O formation than the formation of vanadium / titanium. [00113] Compositions used commercially, especially in mobile applications, comprise TiO 2 in which WO 3 and V 2 O 5 were dispersed in concentrations ranging between 5 to 20% by weight and 0.5 to 6% by weight, respectively. These catalysts can contain other inorganic materials such as SiO 2 and ZrO 2 as binding and promoting agents. [00114] With reference to Figure 1, an exemplary embodiment of a side-spaced system is shown. The SCR 10 catalyst system is shown in a laterally zoned arrangement where the first SCR 18 catalyst composition is located upstream of the second SCR 20 catalyst composition on a common substrate 12. Substrate 12 has an inlet end 22 and an end of outlet 24 defining an axial length L. In one or more embodiments, substrate 12 generally comprises a plurality of channels 14 of a honeycomb substrate, of which only one is shown in the transverse channel for clarity. The first composition of the SCR catalyst 27/39 extends from the inlet end 22 of the substrate 12 to less than the entire axial length L of the substrate 12. The length of the first composition of the SCR catalyst 18 is designated as the first zonal8a in FIG. 1. The first composition of the SCR 18 catalyst may, in the specific embodiments, comprise vanadium / titanium. The second composition of the SCR 20 catalyst may, in the specific embodiments, comprise a small metal-exchanged 8-ring molecular sieve. The second composition of the SCR catalyst 20 extends from the outlet end 24 of the substrate 12 less than the entire axial length L of the substrate 12. The length of the second catalyst composition is denoted as the second zone 20b in Figure 1. The SCR 10 catalyst system is effective for the selective catalytic reduction of NO X. [00115] It will be appreciated that the length of the first zone and the second zone can be varied. In one or more embodiments, the first zone and the second zone can be equal in length. In other modalities, the first zone can be 20%, 25%, 35% or 40%, 60%, 65%, 75% or 80% of the substrate length L, with the second zone, respectively, covering the rest of the length L of the substrate. [00116] Referring to Figure 2, another embodiment of a laterally zoned SCR catalyst system 110 is shown. The SCR 110 catalyst system is shown in a laterally zoned arrangement in which the first SCR 118 catalyst composition is located upstream of the second SCR 120 catalyst composition on separate substrates 112 and 113. The first SCR 118 catalyst composition is arranged on a substrate 112, and the second composition of the SCR catalyst is arranged on a separate substrate 113. Substrates 112 and 113 can be made up of the same or a different material. Substrate 112 has an inlet end 122a and 28/39 an outlet end 124a defining an axial length L1. The substrate 113 has an input end 122b and an output end 124b defining an axial length L2. In one or more embodiments, the supports 112 and 113 generally comprise a plurality of channels 114 of a honeycomb substrate, of which only one channel is shown in cross section, for clarity. The first composition of the SCR catalyst 118 extends from the inlet end 122a of the substrate 112 through the entire axial length L1 of the substrate 112 to the outlet end 124a. The length of the first composition of the SCR catalyst 18 is designated as the first zone8a in FIG. 2. The first composition of the SCR 118 catalyst may, in the specific embodiments, comprise vanadium / titanium. The second composition of the SCR 120 catalyst can, in the specific embodiments, comprise a metal-exchanged small 8-ring molecular sieve. The second composition of the SCR catalyst 120 extends from the outlet end 124b of the substrate 113 through the entire axial length L2 of the substrate 113 to the inlet end 122b. The second composition of catalyst 120 defines a second zone 120a. The SCR 110 catalyst system is effective for the selective catalytic reduction of NO X. The length of zones 118a and 120a can be varied as described in relation to Figure 1. [00117] One or more embodiments of the present invention are directed to a selective catalytic reduction (SCR) of the catalyst system comprising a first SCR catalyst composition comprising vanadium / titanium disposed on a substrate and a second SCR catalyst composition comprising a pore molecular sieve small metal-exchanged 8-rings arranged on a substrate, where the first SCR catalyst composition and the second SCR catalyst composition are in a layered or relationship arrangement. In one or more modalities, the first composition 29/39 of the SCR catalyst is layered on top of the second composition of the SCR catalyst. [00118] According to one or more embodiments, the second composition of the SCR catalyst is coated by immersion on a substrate, and then the first composition of the SCR catalyst is coated by immersion in a layer that overlaps the second composition of the SCR catalyst. In one or more embodiments, the layering has been designed to optimize the first catalyst composition / second dry gain catalyst composition for a desirable balance between the benefits of acting as a protective shield and the potential disadvantages of increasing the diffusion barrier. Under low temperatures for prolonged operations, sulfur is a major concern for Cu-CHA catalysts. In comparison, SCR vanadium / titanium (V 2 O 5 / TiO 2 ) catalysts are known to have superior sulfur tolerance. [00119] The first and second compositions of the SCR catalyst can include the compositions as described above. [00120] With reference to Figure 3, an exemplary embodiment of a layered SCR catalyst system 210 is shown. The SCR catalyst system can be in a layered arrangement where the first SCR 218 catalyst composition is layered on top of the second SCR 220 catalyst composition on a common substrate 212. Substrate 212 has an inlet end 222 and an outlet end 224 which defines an axial length L3. In one or more embodiments, substrate 212 generally comprises a plurality of channels 214 of a honeycomb substrate, of which only one channel is shown in cross section, for clarity. The first composition of the SCR 218 catalyst extends from the inlet end 222 of the substrate 212 through the entire axial length L3 of the substrate 212 to the outlet end 224. The length of the first 30/39 SCR 218 catalyst composition is denoted as 218a in FIG. 3. The first composition of the SCR 218 catalyst may, in the specific embodiments, comprise vanadium / titanium. The second composition of the SCR 220 catalyst may, in the specific embodiments, comprise a metal-exchanged 8-ring small pore molecular sieve. The first SCR catalyst composition 220 extends from the inlet end 224 of substrate 212 through the entire axial length L3 of substrate 212 to the outlet end 224. The SCR catalyst system 210 is effective for the selective catalytic reduction of NO X. [00121] It will be appreciated that the thickness of layer 218 can be relatively thin compared to the thickness of layer 220. The thickness of layer 218 can be thick enough to form a protective coating on layer 220 to protect the catalyst composition of the layer 220 sulfation. In one embodiment, the thickness of the composition layer of the first catalyst 218 is 5-10% of the total thickness of the compound layer 218 and 220. In other embodiments, the thickness of the first catalyst composition layer is 20-30% of the thickness total compound layer 218 and 220. In some embodiments, the thickness of the first catalyst composition layer is 30-40% of the total compound layer thickness 218 and 220. Exhaust Gas Treatment System: [00122] In one aspect of the invention, the exhaust gas treatment system comprises a low-combustion engine, and the exhaust gas conduit in fluid communication with the low-combustion engine, and a selective catalytic reduction catalyst system including a first SCR catalyst composition and a second SCR catalyst composition arranged in the system according to one or more embodiments. In 31/39 specific modes, the low-burn engine is a heavy-duty diesel engine. [00123] In one or more modalities, the exhaust gas treatment system includes an exhaust gas flow containing a reducer such as ammonia, urea and / or hydrocarbon, and in specific modalities, ammonia and / or urea. In the specific embodiments, the exhaust gas treatment system further comprises a second exhaust gas treatment component, for example, a particulate filter or a diesel oxidation catalyst. [00124] The soot filter, catalyzed or non-catalyzed, can be upstream or downstream of the SCR catalyst system, according to one or more modalities. The diesel oxidation catalyst in specific modalities is located upstream of the SCR catalyst system, according to one or more modalities. In specific embodiments, the diesel oxidation catalyst and the catalyzed soot filter are upstream from the SCR catalyst system. [00125] In specific modalities, the exhaust is transported from the low-burn engine to a position downstream in the exhaust system, and, in more specific modalities, containing NO X , in which a reducer is added and the gas stream exhaust system with the added reducer is transported to the SCR catalyst system, according to one or more modalities. [00126] In specific embodiments, the soot filter comprises a wall flow filter substrate, in which the channels are blocked alternately, allowing a gas stream entering the channels in one direction (direction of entry) to flow through the walls the channel and exit the channels from the other direction (exit direction). [00127] An ammonia oxidation catalyst can be provided downstream from the SCR catalyst system to remove any ammonia 32/39 unreacted or in excess of the system. In specific embodiments, the AMOX catalyst may comprise a platinum group metal such as platinum, palladium, rhodium or combinations thereof. In a more specific embodiment, the AMOX catalyst can include an immersion coating containing SCR catalyst system includes a first SCR catalyst composition disposed on a substrate and a second SCR catalyst composition disposed on a substrate. [00128] AMOX and / or SCR catalyst composition can be coated in the continuous flow in the wall flow filter. If a wall-flow substrate is used, the resulting system will be able to remove particulate matter together with polluting gases. The wall flow filter substrate can be made of materials known in the art, such as cordierite, aluminum titanate or silicon carbide. It will be understood that the loading of the catalytic composition onto a flow substrate by walls will depend on substrate properties, such as porosity and wall thickness and will normally be less than the load on a flow through the substrate. SCR activity: [00129] The invention is now described with reference to the following examples. Before describing several exemplary embodiments of the invention, it should be understood that the invention is not limited to the details of construction or process steps set out in the following description. The invention is capable of other modalities and can be practiced or carried out in various ways. EXAMPLES [00130] Example 1 - Preparation of catalyst materials [00131] Vanadium-Titanium Catalyst [00132] A vanadium / titanium / tungsten standard (V 2 O 5 (2.5%) / WO 3 (10%) / TiO 2 ) of the catalyst was prepared and a suspension was made 33/39 in about 30-40% solids by grinding to provide a dip coating slurry. [00133] Cu-Zeolite [00134] A Cu-CHA powder (SSZ-13) was prepared by mixing 100g of CHA in the form of Na, having an alumina / silica molar ratio of 30, with 400 ml_ of a solution copper (II) acetate of about 1.0 Μ. The pH was adjusted to about 3.5 with nitric acid. An ion exchange reaction was carried out between CHA in the form of Na and copper ions by stirring the paste at about 80 ° C for about 1 hour. The resulting mixture was then filtered to provide a filter cake, and the filter cake was washed with deionized water in three portions until the filtrate was clear and colorless, and the washed sample was dried. [00135] The CuCHA catalyst obtained comprises CuO in a range of about 2.5 to 3.5% by weight, as determined by the ICP analysis. A CuCHA slurry was prepared for 40% target solids. The paste was ground and a zirconium acetate binder in dilute acetic acid (containing 30% ZrO 2 ) was added to the paste with stirring. [00136] EXAMPLE 2- LATERALLY ZONE CATALYST SYSTEM [00137] The pastes described above were coated separately on 12Dx6L cell ceramic substrate having a cell density of 400 cpsi (cells per square inch) and a wall thickness of 4 mil. The coated substrates were dried at 110 ° C for 3 hours and calcined at about 400 ° C for 1 hour. The coating process was repeated once to obtain a target immersion coating load in the range of 3 g / in 3 on the vanadium-titanium coated core, and 2.1 g / in 3 on the CuCHa coated core. Samples were aged for 200 hours at 550 0 C in a diesel engines of heavy duty test. 34/39 [00138] COMPARATIVE EXAMPLE 3- SYSTEM OF THE SIDE ZONE CATALYST [00139] Example 2 was repeated with the exception of both substrates that were coated with CuCHa at the same loading. [00140] EXAMPLE 4- SIDE SYSTEMS LATERALLY ENGINE TESTS [00141] The catalyst systems in Example 3 and 4 were tested out on a 9L heavy duty engine together with an electric motor dynamometer. The test bench is capable of running in both steady state and transient test cycles. In the current work, both a heavy duty transient test cycle (HDTP) and a non-road transient test cycle (NRTC) were performed. Catalyst samples were in full size 12 parts in diameters (400/4), which were 200h-550 ° C with engine age before evaluations. To demonstrate the advantage of the 12x6 V-SCR side zone system upstream of a 12x6 Cu-CHA brick, a sequential 12x6 Cu + 12x6 reference of the SCR system was also evaluated. In a comparative study, only the first SCR catalyst bricks were switched between V-SCR and-Cu-SCR, other systems, such as the second SCR brick, the urea injection system, drill sample locations were kept the same. [00142] During the evaluation tests, two MKS FTIR samplers were positioned in the SCR upstream and downstream, respectively, for gaseous emissions measurements, including, but not limited to, NO, NO2, N2O and etc. exhaust sampling lines were heated to constant 190 ° C. All evaluation tests in this example were performed with ULSD (ultra-low diesel sulfur) fuel, where the sulfur concentration is less than 15 ppm (% by weight). [00143] In one configuration, a diesel oxidation catalyst and catalyzed soot filter were placed upstream of the 35/39 SCR catalyst to simulate a heavy duty engine transient cycle. In another configuration, the SCR catalyst system was tested without catalysts or filters upstream. [00144] Figure 4 shows the results of the HDTP cycle and Figure 5 shows the results of the NRTC cycle. Both tests showed a significant reduction in the emission of N 2 O for the samples in which the vanadium-titania catalyst was placed upstream of the Cu-zeolite sample. [00145] The tests were repeated with an oxidation catalyst upstream of the diesel and catalyzed soot filter. Figure 6 shows the results for the HDTP cycle, and Figure 7 shows the results for the NRTC. Once again, the system with the vanadium-titanium catalyst upstream of the Cu Zeolite system showed much lower N 2 O emissions. EXAMPLE 5 - PREPARATION OF THE LAYER CATALYST SYSTEM [00146] The dip coatings of Example 1 were used and coated on a single substrate in a layered configuration as described in relation to Figure 3. The stratification was varied as for the following samples. Comparative Sample 5A of Single Coated Bowl 2.1 g / in 3 Comparative Sample 5B of CuCHa lower coating 2.1 g / in 3 ; Top coat 0.2 g / in 3 Titanium Sample 5C of CuCHa Bottom Coating - CuCHa 2.1 g / in 3 ; Top Coating 0.1 g / in 3 Vanadium Titanium Sample 5D of the Lower CuCHa Coating of 2.1 g / in 3 ; 0.2 g / 3 Top Coating Titanium Vanadium Sample 5E of the CuCHa Bottom Coating of 2.1 g / in 3 ; Top Coating of 0.5 g / in 3 Vanadium-Titanium 36/39 Sample 5F of the lower coating of the CuCHa of 2.1 g / em3; Top Coat 1 g / in 3 Vanadium Titanium [00147] EXAMPLE 6 - LAYER SYSTEM TEST [00148] Selective catalytic reduction of nitrogen oxides (SCR) in efficiency and selectivity of a fresh catalyst core was measured by adding a feed gas mixture of 500 ppm NO, 500 ppm NH 3 , 10% O 2 , 5% H 2 O, equilibrated with N 2 to a reactor containing a steady state of the 1D x 3 catalyst core. The reaction was carried out at a spatial speed of 80,000 l 1 across a temperature range of 150 ° C to 460 ° C. [00149] The samples were hydrothermally aged in the presence of 10% H 2 O at 550 ° C for 4 hours, followed by measuring the efficiency and selectivity of SCR of nitrogen oxides by the same process as described above for the evaluation of SCR in a new catalyst core. [00150] Selective catalytic reduction of nitrogen oxides (SCR) in efficiency and selectivity of a fresh catalyst core was measured by adding a feed gas mixture of 500 ppm NO, 500 ppm NH 3 , 10% O2, 5% H2O, balanced with N2 to a steady state reactor containing the catalyst core 1L x 3 the reaction was carried out at a space velocity of 80,000 SL 1 through a temperature range 150 ° C up to 460 ° C. [00151] Samples prepared as described above were tested for SCR performance. In addition, all samples except for 5F were exposed to sulfur (sulfation) in 300 0 C at 20 ppm SO 2 and 5% H 2 O and 10% O 2 in a feed gas upstream of a core of DOC with SCR catalysts downstream for 6 hours. [00152] FIG. 8 shows the conversion of NO X as a function of temperature, for samples 5A-F before sulfation and Figure 9 shows the 37/39 conversion of NO X as a function of temperature, after sulfation. Fresh conversions were comparable for all samples, except for the 5F sample. For the sulfated sample, Figure 9 shows that sample 5E had significantly better conversion of NO x . [00153] EXAMPLE 9 Dynamic Response Modeling [00154] Figures 10 and 11 illustrate the improvements in the dynamic response behavior of a system according to one or more modalities. Figures 10 and 11 were prepared using a computer model. The performance measurements of the Lab and lab motor DeNO x reactor to describe the performance of the individual components within the system are the inputs for the computer model used. The example in Figure 10 shows the performance of DeNO x as a function of the time obtained with fresh systems without ammonia stored before the start of the simulation / urea dosage. A Cu-SSZ13 system and a vanadium-based SCR system are compared with the Vanadium / Cu-SSZ-13 hybrid system. The Vanadium-based SCR catalyst was placed in front of the Cu-SSZ13 catalyst with a 50/50 size ratio within the modeled hybrid system. Low temperature operation at 225 ° C and escape temperature of 50000 for 1 / h of the space speed at 500ppm at the NO x inlet concentration in a NO 2 / NO X ratio of 10% was used for the comparison. These SCR entry conditions can be seen as being typical for systems operated in motor applications with a low precious metal load from an oxidation system in front of the RCS or only in SCR systems. The NSR was chosen in 1.1, in order to achieve the maximum DeNO x performance of the studied systems relatively quickly. Although the Cu-SSZ13 system achieves greater DeNO x performance after 700 seconds of dosing, the response behavior of DeNO x after the start of application of doses in 0 seconds has a different classification. The response of the Vanadium-based SCR system is faster 38/39 in relation to the increase in DeNO x after starting dosing compared to the Cu-SSZ13 system (for example, up to 350 seconds). The SCR based on the Vanadium hybrid system in combination with the CuSSZ13 has the advantage of being close to the dynamic response behavior of the Vanadium-based SCR and, in addition, offering greater steady state to the performance of the Deno x , as shown in Figure 10, after , for example, 1000 seconds. [00155] Figure 11 was generated by re-tracing Figure 10 using the total NH 3 adsorbed on the catalysts, in grams, as the results for the x-axis. The practical advantage of the hybrid system can be seen when comparing the necessary ammonia stored in the catalysts to achieve, for example, 70% of DeNO x . The CuSSZ13 system needs approximately 4.5 g NH 3 , while the Vanadium-based system would require approximately 2.5 g, and the proposed hybrid system approximately 3 g of stored ammonia. The hybrid system, therefore, would deliver DeNO x performance faster and with lower NH 3 storage levels compared to the Cu-SSZ13 SCR system. In addition, the hybrid system would deliver the higher steady-state performance of DeNO x compared to the Vanadium-based SCR system. The higher DeNO x performance achieved at lower NH 3 storage levels has an additional advantage when the engine accelerates with sudden increases in exhaust temperature. In this case, the amount of ammonia desorbed from the catalysts as a function of the temperature increase is lower for the hybrid system compared to the Cu-SSZ13 system and, therefore, would result in lower slip values of NH 3 behind the part of After treatment system SCR. Even when an ammonia oxidation catalyst is used to control the NH 3 slip from the SCR, very high ammonia peaks from acceleration events are often problems for the 39/39 ammonia oxidation catalyst, due to the typical volumes installed in combination with the ammonia erasure characteristics. [00156] References throughout this specification to a modality, certain modalities, one or more modalities or modality mean that a specific feature, structure, material or resource described in relation to the modality is included in at least one modality of the invention. In this way, the appearances of the phrases as in one or more modalities, in certain modalities, in one modality, or in the modality in several places throughout this specification are not necessarily referring to the same modality of the invention. Furthermore, specific resources, structures, materials or characteristics can be combined in any suitable way in one or more modalities. Although the invention of this document has been described with reference to specific modalities, it should be understood that these modalities are merely illustrative of the principles and applications of the present invention. It will be apparent to those skilled in the art that various modifications and variations can be made to the methods and apparatus of the present invention without departing from the spirit and scope of the invention. Thus, it is intended that the present invention includes modifications and variations that are within the scope of the appended claims and their equivalents.
权利要求:
Claims (15) [1] 1. Catalyst selective catalytic reduction (SCR) system characterized by the fact that it comprises a first composition of the SCR catalyst and a second composition of the SCR catalyst arranged in the system, the first composition of the SCR catalyst promoting greater formation of N 2 and lower formation of N 2 O than the second SCR catalyst composition, and the second SCR catalyst composition having a different composition than the first SCR catalyst composition, the second SCR catalyst composition promoting the lower formation of N 2 and the greater formation of N 2 O than the first SCR catalyst composition, wherein the first SCR catalyst composition and the second SCR catalyst composition are in a layered relationship, with the first layered SCR catalyst composition on top of the second SCR catalyst composition. [2] 2. SCR catalyst system according to claim 1, characterized by the fact that the first composition of the SCR catalyst comprises a mixed oxide. [3] 3. SCR catalyst system according to claim 2, characterized by the fact that the mixed oxide is selected from Fe / titanium, Fe / alumina, Mg / titanium, Cu / titanium, Ce / Zr, vanadium / titanium, and their mixtures. [4] The SCR catalyst system of claims 2 or 3, characterized in that the mixed oxide comprises vanadium / titanium. [5] SCR catalyst system according to claim 3 or 4, characterized in that the vanadium / titanium is stabilized with tungsten. [6] 6. SCR catalyst system according to any one of claims 1 to 5, characterized by the fact that the second 2/3 SCR catalyst comprises a metal-exchanged small ring-8 molecular pore sieve. [7] 7. Selective catalytic reduction (SCR) of the catalyst system characterized by the fact that it comprises a first SCR catalyst composition comprising vanadium / titanium disposed on a substrate and a second SCR catalyst composition comprising a metal-exchanged small 8-ring molecular sieve arranged on a substrate, where the first SCR catalyst composition and the second SCR catalyst composition are in a layered relationship, with the first layered SCR catalyst composition on top of the second SCR catalyst composition. [8] 8. SCR catalyst system according to claims 6 or 7, characterized by the fact that the molecular sieve has a type of structure selected from the group consisting of AEI, AFT, AFX, CHA, EAB, HE, KFI, LEV, SAS , SAT, DDR and SAV. [9] The SCR catalyst system of any one of claims 6 to 8, characterized by the fact that the molecular sieve is an aluminosilicate zeolite and has a CHA-like structure. [10] 10. Catalyst according to claim 9, characterized by the fact that the zeolite is selected from SSZ-13 and SSZ-62. [11] 11. Catalyst system according to any one of claims 6 to 10, characterized by the fact that the metal is selected from the group consisting of Cu, Fe, Co, Ni and Ce. [12] Catalyst system according to any one of claims 6 to 11, characterized in that the metal is selected from Cu and is changed in the range of 2% to 8% by weight. [13] 13. Catalyst system according to claim 7, characterized by the fact that vanadium / titanium promotes higher N 2 formation and lower N 2 O formation than the 8-ring small metal-exchanged molecular sieve ring, and in which the 8-ring pore of metal-exchanged molecular sieve promotes lower, N 2 and 3/3 formation of a greater amount of N 2 Formation S than vanadium / titanium oxide, and the 8-pore metal-exchanged small molecular sieve ring has a greater ammonia storage capacity than vanadium / titanium. [14] 14. Exhaust gas-poor engine system comprises the treatment of the catalyst system according to any one of claims 1 to 14, characterized by the fact that it comprises a poor-combustion engine and a communication exhaust gas duct fluid with the lean-burn engine, where the catalyst system is downstream of the engine. [15] 15. Method of removing nitrogen oxides from the exhaust gases of a lean-burn engine, the method is characterized by the fact that it comprises the contact of an exhaust gas flow from the catalyst system according to any of the claims 1 to 13.
类似技术:
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同族专利:
公开号 | 公开日 CN105026038B|2018-09-28| RU2015143694A|2017-04-20| US9017626B2|2015-04-28| CN105026038A|2015-11-04| KR102280961B1|2021-07-26| MX2015011264A|2016-04-28| JP6470734B2|2019-02-13| CA2900291A1|2014-10-02| JP2016517348A|2016-06-16| WO2014160289A1|2014-10-02| KR20150128698A|2015-11-18| ZA201507599B|2017-11-29| US20140301923A1|2014-10-09|
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法律状态:
2018-11-13| B06F| Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]| 2019-09-17| B15I| Others concerning applications: loss of priority|Free format text: PERDA DA PRIORIDADE US14/208,817, DE 13/03/2014, REIVINDICADA NO PCT/US2014/026243, DE 13/03/2014, TENDO EM VISTA O PRAZO DEFINIDO NO ART. 4O DA CONVENCAO DA UNIAO DE PARIS. | 2020-07-28| B06U| Preliminary requirement: requests with searches performed by other patent offices: procedure suspended [chapter 6.21 patent gazette]| 2021-06-29| B06A| Patent application procedure suspended [chapter 6.1 patent gazette]| 2021-10-05| B350| Update of information on the portal [chapter 15.35 patent gazette]| 2021-11-03| B07A| Application suspended after technical examination (opinion) [chapter 7.1 patent gazette]|
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