US20070119153A1 - Superheated urea injection for aftertreatment applications - Google Patents

Superheated urea injection for aftertreatment applications Download PDF

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US20070119153A1
US20070119153A1 US11/289,261 US28926105A US2007119153A1 US 20070119153 A1 US20070119153 A1 US 20070119153A1 US 28926105 A US28926105 A US 28926105A US 2007119153 A1 US2007119153 A1 US 2007119153A1
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Prior art keywords
urea
scr system
injection
urea scr
catalyst
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US11/289,261
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Patrick Pierz
Laszlo Tikk
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Cummins Filtration Inc
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Fleetguard Inc
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Priority to US11/289,261 priority Critical patent/US20070119153A1/en
Assigned to FLEETGUARD, INC. reassignment FLEETGUARD, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: TIKK, LASZLO D., PIERZ, PATRICK
Priority to DE102006049591A priority patent/DE102006049591A1/en
Publication of US20070119153A1 publication Critical patent/US20070119153A1/en
Abandoned legal-status Critical Current

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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation 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
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/92Chemical or biological purification of waste gases of engine exhaust gases
    • B01D53/94Chemical or biological purification of waste gases of engine exhaust gases by catalytic processes
    • B01D53/9404Removing only nitrogen compounds
    • B01D53/9409Nitrogen oxides
    • B01D53/9431Processes characterised by a specific device
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation 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
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/74General processes for purification of waste gases; Apparatus or devices specially adapted therefor
    • B01D53/86Catalytic processes
    • B01D53/90Injecting reactants
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F01MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
    • F01NGAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
    • F01N3/00Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust
    • F01N3/08Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous
    • F01N3/10Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous by thermal or catalytic conversion of noxious components of exhaust
    • F01N3/18Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous by thermal or catalytic conversion of noxious components of exhaust characterised by methods of operation; Control
    • F01N3/20Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous by thermal or catalytic conversion of noxious components of exhaust characterised by methods of operation; Control specially adapted for catalytic conversion ; Methods of operation or control of catalytic converters
    • F01N3/2066Selective catalytic reduction [SCR]
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2251/00Reactants
    • B01D2251/20Reductants
    • B01D2251/206Ammonium compounds
    • B01D2251/2067Urea
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F01MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
    • F01NGAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
    • F01N2390/00Arrangements for controlling or regulating exhaust apparatus
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F01MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
    • F01NGAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
    • F01N2610/00Adding substances to exhaust gases
    • F01N2610/02Adding substances to exhaust gases the substance being ammonia or urea
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F01MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
    • F01NGAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
    • F01N2610/00Adding substances to exhaust gases
    • F01N2610/10Adding substances to exhaust gases the substance being heated, e.g. by heating tank or supply line of the added substance
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02TCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
    • Y02T10/00Road transport of goods or passengers
    • Y02T10/10Internal combustion engine [ICE] based vehicles
    • Y02T10/12Improving ICE efficiencies

Definitions

  • the present invention relates in general to internal combustion engine technology and to reducing the level of NO x emission by selected catalytic reduction (SCR). More specifically, the present invention relates to the use of urea injection upstream from the SCR site, in the vehicle exhaust stream, as part of an urea SCR exhaust aftertreatment system and approach for a diesel engine.
  • SCR selected catalytic reduction
  • urea SCR exhaust aftertreatment may be one of the more cost-effective approaches while still providing effective NO x reduction.
  • Selective Catalytic Reduction (SCR) technology injects a reduction agent into the exhaust upstream of a catalyst. On the catalyst, the NO x , is reduced to N 2 (nitrogen) and H 2 O (water).
  • One of the first reduction agents used was anhydrous ammonia (NH 3 ).
  • urea SCR reduction the basic chemical reactions are well known.
  • the urea solution atomizes and dissolves as ammonia (NH 3 ) and carbon dioxide (CO 2 ). Then, the NH 3 reacts with NO and NO 2 in the exhaust gas to reduce to N 2 (nitrogen) and H 2 O (water).
  • the approach selected to address these concerns is to use superheated fuel injection.
  • the system includes a fuel supply upstream of a pressurized fuel injector and a heater for heating the fuel in the pressurized fuel supply. While this approach offers one option for NO x reduction, it does not provide a urea-based system. This approach also requires a fuel supply, fuel injector, heater, and controller to monitor the temperature.
  • Prior art urea SCR systems as noted, rely on the exhaust to heat the urea solution to achieve atomization and dissolving of the urea solution into ammonia and carbon dioxide.
  • the present invention proposes a novel and unobvious approach.
  • the urea solution is preheated and pressurized to superheated conditions prior to injection into the exhaust, thereby avoiding any dependency or reliance on heat from the exhaust in order to vaporize the urea solution.
  • Another benefit from this approach is that the atomized urea solution is in the form of a very fine mist (steam), providing improved distribution as compared to the results using larger liquid droplets of urea.
  • the vaporized urea solution now as a very fine mist or steam, can be injected closer to the catalyst and conceivably at lower temperatures. This also helps to reduce or minimize the package length. Yet another benefit is that the nozzle hole can be larger and it will thereby not be as prone to plugging as when it functions as an essential part of the atomization process.
  • An urea SCR system for enhancing internal combustion engine aftertreatment applications comprises a supply of urea solution, a delivery pump for delivering urea solution into an exhaust stream at an injection location, and a heating device positioned between the supply of urea solution and the injection location for preheating the urea solution prior to injection into the exhaust stream.
  • One object of the present invention is to provide an improved urea SCR system.
  • FIG. 1 is a schematic illustration of an urea SCR system according to one embodiment of the present invention.
  • Urea SCR system 20 includes a supply 21 of aqueous urea, a pressurizing delivery pump 22 , a heating location or station 23 , and a valve-controlled injection nozzle 24 . Also illustrated in FIG. 1 is an exhaust conduit 25 of a diesel engine (not illustrated) and a selective catalytic reduction (SCR) site 26 . Briefly, the operation or functioning of system 20 begins with an amount of aqueous urea being drawn from supply 21 and delivered downstream to or through heating station 23 by means of delivery pump 22 .
  • Heating station 23 defines a flow passage around a glow plug that functions to heat (preheat) the aqueous urea to an elevated temperature between approximately 130° C. and 220° C., preferably 200° C.
  • the aqueous urea (i.e., urea solution) needs to be preheated to a temperature above the boiling point of the solution at the pressure that exists in the exhaust system or exhaust stream at the point of injection into the exhaust. While the preferred embodiment selects a glow plug as the heating device, the urea solution can also be heated prior to injection by heat from the exhaust, by the engine coolant, or by other electrical resistance devices.
  • the urea solution When the heated and pressurized urea solution is injected into the lower pressure of the exhaust stream, the urea solution instantly flashes to steam and the fine mist of urea that is desired is thereby achieved. While the heated urea solution remains in the connecting flow conduit upstream of the injection nozzle 24 , the elevated pressure keeps the urea solution in a liquid state. As noted, the liquid state changes to steam when the urea solution hits the lower exhaust pressure.
  • a urea solution temperature of approximately 200° C. is considered to be a superheated condition.
  • the superheated urea solution flashes to steam in the exhaust stream, it uniformly mixes with the exhaust gas, and the urea solution dissolves as ammonia (NH 3 ) and carbon dioxide (CO 2 ) according to the following: (NH 3 ) 2 +CO+H 2 O ⁇ CO S +2NH 3 .
  • NH 3 reacts with NO and NO 2 in the exhaust gas according to the following: 4NH 3 +4NO+O 2 ⁇ 4N 2 +6H 2 O.
  • 8NH 3 +6NO 2 ⁇ 7N 2 +12H 2 O are acceptable in terms of emissions, and thus one challenge is to try and estimate, as precisely as possible, the amounts of NO and NO 2 in the exhaust gas.
  • the disclosed system 20 provides various benefits to those designing diesel engine systems in order to address emissions reduction.
  • the time in the exhaust stream prior to the SCR site can be shortened. This shortening translates into a shorter distance between the injection location and the SCR site and a reduced package length.
  • a related benefit of creating the vaporized urea solution by superheating is that the delivery nozzle opening can be comparatively larger since the nozzle does not need to participate in the atomization or vaporizing process. By making the injection nozzle hole larger, it will not be as prone to clogging or plugging.
  • the component parts and system subassemblies include the supply 21 of aqueous urea, delivery pump 22 , heating station 23 , and valve-controlled injection nozzle 24 .
  • the supply 21 includes a storage tank 21 a that is flow coupled to the delivery pump 22 by conduit 30 .
  • the proportions or strength of the urea-water solution are not considered to be critical, but the preferred composition is approximately 32.5% urea and 67.5% water.
  • the volume of tank 21 a varies depending on the application and will typically range from 10 liters to approximately 100 liters or perhaps a little higher.
  • the tank 21 a includes a heating element (not illustrated) to ensure that the urea solution stays in a liquid state when injection is required.
  • a filter (not illustrated) is included as part of the construction of tank 21 a to ensure that any contaminants entering tank 21 a are not allowed to enter the downstream remainder of system 20 .
  • the lines carrying the urea solution to the delivery pump 22 are constructed out of a material that is compatible with the urea solution such as rubber, Teflon®, and stainless steel. It is recommended that these conduits or lines include a method to warm them when the ambient temperature falls below the freezing point for the urea-water solution.
  • the delivery pump 22 draws aqueous urea out of storage tank 21 a and pushes it forward with an elevated pressure of approximately 50 psi.
  • the pump needs to increase the pressure to a level sufficient to maintain the urea-water solution in a liquid state when the temperature is raised above the boiling point at normal atmospheric pressure.
  • Conduit 31 connects the delivery pump outlet 32 with control valve 33 prior to injection nozzle 24 .
  • the heating station includes a glow plug 34 that is positioned in a section of conduit 31 in order to heat the flow of aqueous urea.
  • the glow plug 34 elevates the aqueous urea temperature to approximately 200° C. and this elevated temperature, combined with the elevated pressure, creates a very fine mist (steam) as the urea solution is injected by nozzle 24 into the exhaust stream.
  • the reference herein to the SCR site describes the location of the catalyst which is in the exhaust stream, downstream from where the reduction agent (urea solution steam) is injected.
  • Contact with the catalyst by the reduction agent and the exhaust i.e., “on the catalyst”, causes the NO x to be reduced to N 2 (nitrogen) and H 2 O (water).
  • urea is readily available and it is a non-hazardous product. While an aqueous solution of urea has previously been used as a reducing agent, the technique of preheating or superheating the solution is believed to be novel and this approach, as presented by the present invention, very clearly provides benefits to the customer, as described herein.

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  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Environmental & Geological Engineering (AREA)
  • Analytical Chemistry (AREA)
  • Combustion & Propulsion (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • General Chemical & Material Sciences (AREA)
  • Biomedical Technology (AREA)
  • Toxicology (AREA)
  • General Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Exhaust Gas After Treatment (AREA)

Abstract

An urea SCR system for enhancing internal combustion engine aftertreatment applications includes a supply tank containing aqueous urea, a delivery pump operatively connected to the supply tank and configured for elevating the pressure of aqueous urea drawn from said supply tank. The urea SCR system further includes a conduit arrangement connecting the delivery pump to an injection nozzle which is positioned adjacent an exhaust stream, the conduit arrangement being configured for the delivery of aqueous urea to the injection nozzle. Downstream of the delivery pump and upstream from the injection nozzle, a heating element is positioned for preheating of the aqueous urea to a superheated condition prior to injection into the exhaust stream.

Description

    BACKGROUND OF THE INVENTION
  • The present invention relates in general to internal combustion engine technology and to reducing the level of NOx emission by selected catalytic reduction (SCR). More specifically, the present invention relates to the use of urea injection upstream from the SCR site, in the vehicle exhaust stream, as part of an urea SCR exhaust aftertreatment system and approach for a diesel engine.
  • Reducing NOx (NO and NO2) emission in diesel exhaust gas has been a major challenge during the past several years and will continue to be a major focus in the future due to the continuing stringent emission requirements for diesel engines. Engine exhaust NOx reduction can be achieved in part by more optimal or more complete combustion and in part by exhaust gas aftertreatment. While these two approaches remain compatible, combustion optimization has NOx reduction limits and alone will likely not be able to meet the EPA proposed levels for the future, such as the U.S. 2007 heavy-duty diesel emission standard. Accordingly, some degree of exhaust gas aftertreatment will be required in order to achieve the requisite reductions.
  • Considering some of the available aftertreatment technologies, urea SCR exhaust aftertreatment may be one of the more cost-effective approaches while still providing effective NOx reduction. Selective Catalytic Reduction (SCR) technology injects a reduction agent into the exhaust upstream of a catalyst. On the catalyst, the NOx, is reduced to N2 (nitrogen) and H2O (water). One of the first reduction agents used was anhydrous ammonia (NH3).
  • In terms of urea SCR reduction, the basic chemical reactions are well known. When mixing with the exhaust gas beyond a certain temperature, the urea solution atomizes and dissolves as ammonia (NH3) and carbon dioxide (CO2). Then, the NH3 reacts with NO and NO2 in the exhaust gas to reduce to N2 (nitrogen) and H2O (water).
  • While atomization of the urea solution is important, the approach described in terms of the prior art requires an exhaust temperature sufficient for the urea solution to atomize and dissolve as ammonia and carbon dioxide. Some time must elapse following injection for this process to occur, and thus the physical site of urea injection must be far enough upstream from the catalyst for the urea solution to be heated and reach the necessary temperature for atomization and for dissolving into ammonia and carbon dioxide. It is also recognized that the finer or small the urea droplets due to atomization, the more effective and efficient the NOx reduction as a result of this urea SCR technology.
  • In U.S. Patent No. 6,922,987, issued Aug. 2, 2005 to Mital et al., it is stated that NOx adsorber catalysts have the potential for great NOx emission reduction (70-90%) and for extending engine life. However, low temperature operation of adsorbers seems to be a problem. The main reason for this problem seems to be the fact that the reductants, especially D2 fuel, starts to boil at around 180 degrees Celsius. At temperatures below this, the injected fuel has a strong tendency to condense and does not participate in the release and reduction step of NOx adsorbers (catalytic converters). Also, if the droplet size is large, atomization is not good and the fuel does not vaporize easily even at the higher temperature, thereby limiting adsorber performance.
  • Current devices on their own, such as spraying system nozzles and injectors cannot do anything about the condensation at low temperature. Also, the droplet size measurement shows that they have a sauter mean diameter (SMD) in the range of 30-60 μm. If this droplet size can be reduced further, the vaporization will become faster and easier. This will improve the reductant participation in the catalyst reactions and improve the NOx adsorber capacity and NOx conversion efficiency.
  • The approach selected to address these concerns, as described in the '987 patent, is to use superheated fuel injection. The system includes a fuel supply upstream of a pressurized fuel injector and a heater for heating the fuel in the pressurized fuel supply. While this approach offers one option for NOx reduction, it does not provide a urea-based system. This approach also requires a fuel supply, fuel injector, heater, and controller to monitor the temperature. Prior art urea SCR systems, as noted, rely on the exhaust to heat the urea solution to achieve atomization and dissolving of the urea solution into ammonia and carbon dioxide.
  • In order to eliminate any concerns regarding whether the exhaust temperature will be sufficient and the length of time in the exhaust stream adequate to atomize and dissolve the urea solution, the present invention proposes a novel and unobvious approach. According to the present invention, the urea solution is preheated and pressurized to superheated conditions prior to injection into the exhaust, thereby avoiding any dependency or reliance on heat from the exhaust in order to vaporize the urea solution. Another benefit from this approach is that the atomized urea solution is in the form of a very fine mist (steam), providing improved distribution as compared to the results using larger liquid droplets of urea.
  • Yet another benefit from this approach is that the vaporized urea solution, now as a very fine mist or steam, can be injected closer to the catalyst and conceivably at lower temperatures. This also helps to reduce or minimize the package length. Yet another benefit is that the nozzle hole can be larger and it will thereby not be as prone to plugging as when it functions as an essential part of the atomization process.
  • BRIEF SUMMARY OF THE INVENTION
  • An urea SCR system for enhancing internal combustion engine aftertreatment applications according to one embodiment of the present invention comprises a supply of urea solution, a delivery pump for delivering urea solution into an exhaust stream at an injection location, and a heating device positioned between the supply of urea solution and the injection location for preheating the urea solution prior to injection into the exhaust stream.
  • One object of the present invention is to provide an improved urea SCR system.
  • Related objects and advantages of the present invention will be apparent from the following description.
  • BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWINGS
  • FIG. 1 is a schematic illustration of an urea SCR system according to one embodiment of the present invention.
  • DETAILED DESCRIPTION OF THE INVENTION
  • For the purposes of promoting an understanding of the principles of the invention, reference will now be made to the embodiments illustrated in the drawings and specific language will be used to describe the same. It will nevertheless be understood that no limitation of the scope of the invention is thereby intended, such alterations and further modifications in the illustrated device, and such further applications of the principles of the invention as illustrated therein being contemplated as would normally occur to one skilled in the art to which the invention relates.
  • Referring to FIG. 1, there is illustrated an urea SCR system for enhancing internal combustion engine aftertreatment applications. Urea SCR system 20 includes a supply 21 of aqueous urea, a pressurizing delivery pump 22, a heating location or station 23, and a valve-controlled injection nozzle 24. Also illustrated in FIG. 1 is an exhaust conduit 25 of a diesel engine (not illustrated) and a selective catalytic reduction (SCR) site 26. Briefly, the operation or functioning of system 20 begins with an amount of aqueous urea being drawn from supply 21 and delivered downstream to or through heating station 23 by means of delivery pump 22. This delivery or pumping action increases the pressure of the aqueous urea to approximately 50 psi as it enters the heating station 23. Heating station 23 defines a flow passage around a glow plug that functions to heat (preheat) the aqueous urea to an elevated temperature between approximately 130° C. and 220° C., preferably 200° C.
  • More specifically, the aqueous urea (i.e., urea solution) needs to be preheated to a temperature above the boiling point of the solution at the pressure that exists in the exhaust system or exhaust stream at the point of injection into the exhaust. While the preferred embodiment selects a glow plug as the heating device, the urea solution can also be heated prior to injection by heat from the exhaust, by the engine coolant, or by other electrical resistance devices.
  • When the heated and pressurized urea solution is injected into the lower pressure of the exhaust stream, the urea solution instantly flashes to steam and the fine mist of urea that is desired is thereby achieved. While the heated urea solution remains in the connecting flow conduit upstream of the injection nozzle 24, the elevated pressure keeps the urea solution in a liquid state. As noted, the liquid state changes to steam when the urea solution hits the lower exhaust pressure.
  • A urea solution temperature of approximately 200° C. is considered to be a superheated condition. When the superheated urea solution flashes to steam in the exhaust stream, it uniformly mixes with the exhaust gas, and the urea solution dissolves as ammonia (NH3) and carbon dioxide (CO2) according to the following:
    (NH3)2+CO+H2O→COS+2NH3.
    Then, NH3 reacts with NO and NO2 in the exhaust gas according to the following:
    4NH3+4NO+O2→4N2+6H2O.
    8NH3+6NO2→7N2+12H2O.
    These end products or by-products of the reaction are acceptable in terms of emissions, and thus one challenge is to try and estimate, as precisely as possible, the amounts of NO and NO2 in the exhaust gas.
  • The disclosed system 20 provides various benefits to those designing diesel engine systems in order to address emissions reduction. First, the availability and cost of urea, as compared to more expensive alternatives, provides a cost benefit to the customer. Secondly, by not requiring the exhaust stream to provide the heating of the urea after injection, the time in the exhaust stream prior to the SCR site can be shortened. This shortening translates into a shorter distance between the injection location and the SCR site and a reduced package length. Thirdly, since system 20 does not rely on heat from the exhaust stream to vaporize the urea solution, the urea solution could conceivably be injected at a comparatively lower temperature. A related benefit of creating the vaporized urea solution by superheating is that the delivery nozzle opening can be comparatively larger since the nozzle does not need to participate in the atomization or vaporizing process. By making the injection nozzle hole larger, it will not be as prone to clogging or plugging.
  • The component parts and system subassemblies include the supply 21 of aqueous urea, delivery pump 22, heating station 23, and valve-controlled injection nozzle 24. The supply 21 includes a storage tank 21 a that is flow coupled to the delivery pump 22 by conduit 30.
  • The proportions or strength of the urea-water solution are not considered to be critical, but the preferred composition is approximately 32.5% urea and 67.5% water. The volume of tank 21 a varies depending on the application and will typically range from 10 liters to approximately 100 liters or perhaps a little higher. The tank 21 a includes a heating element (not illustrated) to ensure that the urea solution stays in a liquid state when injection is required. A filter (not illustrated) is included as part of the construction of tank 21 a to ensure that any contaminants entering tank 21 a are not allowed to enter the downstream remainder of system 20.
  • The lines carrying the urea solution to the delivery pump 22 are constructed out of a material that is compatible with the urea solution such as rubber, Teflon®, and stainless steel. It is recommended that these conduits or lines include a method to warm them when the ambient temperature falls below the freezing point for the urea-water solution.
  • The delivery pump 22 draws aqueous urea out of storage tank 21 a and pushes it forward with an elevated pressure of approximately 50 psi. The pump needs to increase the pressure to a level sufficient to maintain the urea-water solution in a liquid state when the temperature is raised above the boiling point at normal atmospheric pressure.
  • Conduit 31 connects the delivery pump outlet 32 with control valve 33 prior to injection nozzle 24. The heating station includes a glow plug 34 that is positioned in a section of conduit 31 in order to heat the flow of aqueous urea. The glow plug 34 elevates the aqueous urea temperature to approximately 200° C. and this elevated temperature, combined with the elevated pressure, creates a very fine mist (steam) as the urea solution is injected by nozzle 24 into the exhaust stream.
  • The reference herein to the SCR site describes the location of the catalyst which is in the exhaust stream, downstream from where the reduction agent (urea solution steam) is injected. Contact with the catalyst by the reduction agent and the exhaust, i.e., “on the catalyst”, causes the NOx to be reduced to N2 (nitrogen) and H2O (water). In terms of available reducing agents, urea is readily available and it is a non-hazardous product. While an aqueous solution of urea has previously been used as a reducing agent, the technique of preheating or superheating the solution is believed to be novel and this approach, as presented by the present invention, very clearly provides benefits to the customer, as described herein.
  • While the invention has been illustrated and described in detail in the drawings and foregoing description, the same is to be considered as illustrative and not restrictive in character, it being understood that only the preferred embodiment has been shown and described and that all changes and modifications that come within the spirit of the invention are desired to be protected.

Claims (17)

1. An urea SCR system for enhancing internal combustion engine aftertreatment applications, said urea SCR system comprising:
a supply of urea solution;
delivery means for delivering urea solution into an exhaust stream at an injection location; and
heating means positioned between said supply of urea solution and said injection location for preheating urea solution prior to injection into said exhaust stream.
2. The urea SCR system of claim 1 which further includes a delivery pump flow coupled to said supply of urea solution.
3. The urea SCR system of claim 2 which further includes an injection nozzle adjacent said injection location.
4. The urea SCR system of claim 3 wherein said heating means includes a glow plug.
5. The urea SCR system of claim 4 wherein said preheating corresponds to a superheated condition for said urea solution.
6. The urea SCR system of claim 5 wherein said exhaust stream includes a catalyst and said injection location is upstream of said catalyst.
7. The urea SCR system of claim 1 which further includes an injection nozzle adjacent said injection location.
8. The urea SCR system of claim 1 wherein said heating means includes a glow plug.
9. The urea SCR system of claim 1 wherein said heating means includes a glow plug.
10. The urea SCR system of claim 1 wherein said exhaust stream includes a catalyst and said injection location is upstream of said catalyst.
11. The urea SCR system of claim 1 wherein said urea solution is a mixture of water and urea.
12. An urea SCR system for enhancing internal combustion engine aftertreatment applications, said urea SCR system comprising:
a container holding a supply of aqueous urea;
a delivery pump operatively connected to said container;
a conduit connecting said delivery pump to an injection nozzle for delivery of aqueous urea to said injection nozzle; and
a heating element acting on aqueous urea in said conduit for elevating the temperature of said aqueous urea prior to injection into an exhaust stream by way of said injection nozzle.
13. The urea SCR system of claim 12 wherein said heating element is a glow plug.
14. The urea SCR system of claim 13 wherein said elevating of the temperature of said aqueous urea raises said temperature to a superheated condition.
15. The urea SCR system of claim 14 wherein said exhaust stream includes a catalyst and the location of said injection nozzle defines an injection location, said injection location being upstream of said catalyst.
16. The urea SCR system of claim 12 wherein said elevating of the temperature of said aqueous urea raises said temperature to a superheated condition.
17. The urea SCR system of claim 12 wherein said exhaust stream includes a catalyst and the location of said injection nozzle defines an injection location, said injection location being upstream of said catalyst.
US11/289,261 2005-11-29 2005-11-29 Superheated urea injection for aftertreatment applications Abandoned US20070119153A1 (en)

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US11/289,261 US20070119153A1 (en) 2005-11-29 2005-11-29 Superheated urea injection for aftertreatment applications
DE102006049591A DE102006049591A1 (en) 2005-11-29 2006-10-20 Catalytic selective reduction system with urea promotion, for diesel engine exhaust gas, has good cold start performance by upstream injection of electrically preheated aqueous solution in enhanced spray dispersion

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Cited By (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060156733A1 (en) * 2005-01-14 2006-07-20 Pratt & Whitney Canada Corp. Integral heater for fuel conveying member
US20080267837A1 (en) * 2007-04-27 2008-10-30 Phelps Calvin E Conversion of urea to reactants for NOx reduction
US20090084095A1 (en) * 2007-09-28 2009-04-02 Caterpillar Inc. Exhaust after-treatment system having a secondary tank
US20090101631A1 (en) * 2007-10-23 2009-04-23 Farell Tracy M System for controlling high current components in a motor vehicle
US20090133384A1 (en) * 2007-11-26 2009-05-28 Maruthi Devarakonda NOx CONTROL SYSTEMS AND METHODS FOR CONTROLLING NOx EMISSIONS
US20090301064A1 (en) * 2008-06-05 2009-12-10 Eugen Maier Urea pump assembly for an exhaust gas treatment system
US20100107615A1 (en) * 2008-10-31 2010-05-06 Ti Group Automotive Systems, L.L.C. Reactant delivery for engine exhaust gas treatment
US20100304231A1 (en) * 2007-12-27 2010-12-02 Lines Michael T Integrated contaminant6 separator and water-control loop for a fuel reactant stream
US20110233123A1 (en) * 2007-10-01 2011-09-29 Cummins Filtration Ip, Inc. Apparatus, system, and method for filtration of a dosing fluid in an exhaust aftertreatment system
US20110283677A1 (en) * 2008-06-24 2011-11-24 Sebastian Kaefer Exhaust gas posttreatment device for an internal combustion engine
CN102580529A (en) * 2012-02-27 2012-07-18 环境保护部华南环境科学研究所 Electro-pyrolytic urea solution ammonia production device used for selective catalytic denitration and application thereof
WO2013138121A1 (en) * 2012-03-16 2013-09-19 Cummins Inc. Aftertreatment system and method for pre-decomposed reductant solution
JPWO2013153606A1 (en) * 2012-04-09 2015-12-17 トヨタ自動車株式会社 Exhaust gas purification device for internal combustion engine
US9561470B2 (en) 2014-02-14 2017-02-07 Deutz Aktiengesellschaft Method for the purification of diesel engine exhaust gases
US20170058738A1 (en) * 2015-08-28 2017-03-02 General Electric Company Treatment of emissions in power plants
US9695726B2 (en) 2010-12-17 2017-07-04 Daimler Ag Metering arrangement and method for operating a metering arrangement
US20180363527A1 (en) * 2017-06-16 2018-12-20 Watlow Electric Manufacturing Company Temperature-based control of reagent distribution
DE102021104051A1 (en) 2020-02-25 2021-08-26 Caterpillar Inc. REDUCING DIESEL EMISSION LIQUID (DEF) DEPOSIT IN AN EXHAUST SYSTEM FOR AN ENGINE
US11408315B2 (en) * 2020-12-17 2022-08-09 Faurecia Systemes D'echappement Device for injecting a fluid into an exhaust pipe and associated exhaust system

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102007034314B4 (en) * 2007-07-24 2020-10-15 Emcon Technologies Germany (Augsburg) Gmbh Assembly and method for introducing a reducing agent into an exhaust pipe
CN102166472A (en) * 2011-02-25 2011-08-31 中环(中国)工程有限公司 Spiral-flow type ammonia spraying device used for selective catalytic reduction (SCR) denitrification system
EP2568137B1 (en) 2011-09-08 2015-08-05 Ford Global Technologies, LLC Heated injection system for exhaust gas systems of Diesel engines
FR3017653B1 (en) * 2014-02-14 2018-11-02 Psa Automobiles Sa. METHOD FOR CONTROLLING A CATALYTIC REDUCTION SYSTEM INJECTOR
DE102014209373A1 (en) 2014-05-16 2015-11-19 Robert Bosch Gmbh Reducing agent catalytic system
DE102015118147A1 (en) 2015-10-23 2017-04-27 Eberspächer Exhaust Technology GmbH & Co. KG Apparatus and method for dispensing reactant in the exhaust stream of an internal combustion engine
DE102015118572B4 (en) 2015-10-30 2022-10-06 Purem GmbH Method of delivering reactant into the exhaust stream of an internal combustion engine
DE102016100284A1 (en) 2016-01-11 2017-07-13 Eberspächer Exhaust Technology GmbH & Co. KG Exhaust system for an internal combustion engine and method for operating an exhaust system
DE102016210640A1 (en) * 2016-06-15 2017-12-21 Volkswagen Aktiengesellschaft Device and method for dosing a reducing agent in the exhaust passage of an internal combustion engine

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4639871A (en) * 1983-02-03 1987-01-27 Nippondenso Co., Ltd. Glow plug heating control apparatus for a diesel engine
US5809775A (en) * 1997-04-02 1998-09-22 Clean Diesel Technologies, Inc. Reducing NOx emissions from an engine by selective catalytic reduction utilizing solid reagents
US6834498B2 (en) * 2002-11-21 2004-12-28 Ford Global Technologies, Llc Diesel aftertreatment systems
US6837041B2 (en) * 2001-01-13 2005-01-04 Fev Motorentechnik Gmbh Method of converting a solid nitrogen-containing reducing agent to the gas phase for use in the reduction of nitrogen oxides in exhaust gases
US6849829B1 (en) * 1999-12-11 2005-02-01 Robert Bosch Gmbh Glow plug with frustoconical ceramic heating element
US6878359B1 (en) * 1998-05-11 2005-04-12 Siemens Aktiengesellschaft Process and device for the selective catalytic reduction of nitrogen oxides in an oxygen-containing gaseous medium
US6922987B2 (en) * 2003-02-12 2005-08-02 Fleetguard, Inc. System and method for enhancing internal combustion engine aftertreatment applications by superheated fuel injection
US6928807B2 (en) * 2002-02-14 2005-08-16 Man Nutzfahrzeuge Ag Method and apparatus for producing ammonia (NH3)
US7065958B2 (en) * 2002-05-07 2006-06-27 Extengine Transport Systems Emission control system

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4639871A (en) * 1983-02-03 1987-01-27 Nippondenso Co., Ltd. Glow plug heating control apparatus for a diesel engine
US5809775A (en) * 1997-04-02 1998-09-22 Clean Diesel Technologies, Inc. Reducing NOx emissions from an engine by selective catalytic reduction utilizing solid reagents
US6878359B1 (en) * 1998-05-11 2005-04-12 Siemens Aktiengesellschaft Process and device for the selective catalytic reduction of nitrogen oxides in an oxygen-containing gaseous medium
US6849829B1 (en) * 1999-12-11 2005-02-01 Robert Bosch Gmbh Glow plug with frustoconical ceramic heating element
US6837041B2 (en) * 2001-01-13 2005-01-04 Fev Motorentechnik Gmbh Method of converting a solid nitrogen-containing reducing agent to the gas phase for use in the reduction of nitrogen oxides in exhaust gases
US6928807B2 (en) * 2002-02-14 2005-08-16 Man Nutzfahrzeuge Ag Method and apparatus for producing ammonia (NH3)
US7065958B2 (en) * 2002-05-07 2006-06-27 Extengine Transport Systems Emission control system
US6834498B2 (en) * 2002-11-21 2004-12-28 Ford Global Technologies, Llc Diesel aftertreatment systems
US6922987B2 (en) * 2003-02-12 2005-08-02 Fleetguard, Inc. System and method for enhancing internal combustion engine aftertreatment applications by superheated fuel injection

Cited By (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060156733A1 (en) * 2005-01-14 2006-07-20 Pratt & Whitney Canada Corp. Integral heater for fuel conveying member
US8017100B2 (en) 2007-04-27 2011-09-13 Babcock Power Environmental Inc. Conversion of urea to reactants for NOx reduction
US20080267837A1 (en) * 2007-04-27 2008-10-30 Phelps Calvin E Conversion of urea to reactants for NOx reduction
US20100015029A1 (en) * 2007-04-27 2010-01-21 Babcock Power Envoronmental Inc. Conversion of urea to reactants for nox reduction
US20090084095A1 (en) * 2007-09-28 2009-04-02 Caterpillar Inc. Exhaust after-treatment system having a secondary tank
US8096112B2 (en) 2007-09-28 2012-01-17 Caterpillar Inc. Exhaust after-treatment system having a secondary tank
US8524091B2 (en) 2007-10-01 2013-09-03 Kuss Filtration Inc. Apparatus, system, and method for filtration of a dosing fluid in an exhaust aftertreatment system
US20110233123A1 (en) * 2007-10-01 2011-09-29 Cummins Filtration Ip, Inc. Apparatus, system, and method for filtration of a dosing fluid in an exhaust aftertreatment system
US20090101631A1 (en) * 2007-10-23 2009-04-23 Farell Tracy M System for controlling high current components in a motor vehicle
US20090133384A1 (en) * 2007-11-26 2009-05-28 Maruthi Devarakonda NOx CONTROL SYSTEMS AND METHODS FOR CONTROLLING NOx EMISSIONS
US8230677B2 (en) * 2007-11-26 2012-07-31 Michigan Technological University NOx control systems and methods for controlling NOx emissions
US20100304231A1 (en) * 2007-12-27 2010-12-02 Lines Michael T Integrated contaminant6 separator and water-control loop for a fuel reactant stream
US8343256B2 (en) * 2007-12-27 2013-01-01 Utc Power Corporation Integrated contaminant separator and water-control loop for a fuel reactant stream
US20090301064A1 (en) * 2008-06-05 2009-12-10 Eugen Maier Urea pump assembly for an exhaust gas treatment system
US20110283677A1 (en) * 2008-06-24 2011-11-24 Sebastian Kaefer Exhaust gas posttreatment device for an internal combustion engine
US9574478B2 (en) * 2008-06-24 2017-02-21 Robert Bosch Gmbh Exhaust gas posttreatment device for an internal combustion engine
US8359831B2 (en) * 2008-10-31 2013-01-29 Ti Group Automotive Systems, L.L.C. Reactant delivery for engine exhaust gas treatment
US20100107615A1 (en) * 2008-10-31 2010-05-06 Ti Group Automotive Systems, L.L.C. Reactant delivery for engine exhaust gas treatment
US8875493B2 (en) 2008-10-31 2014-11-04 Ti Group Automotive Systems, L.L.C. Reactant delivery for engine exhaust gas treatment
US9695726B2 (en) 2010-12-17 2017-07-04 Daimler Ag Metering arrangement and method for operating a metering arrangement
CN102580529A (en) * 2012-02-27 2012-07-18 环境保护部华南环境科学研究所 Electro-pyrolytic urea solution ammonia production device used for selective catalytic denitration and application thereof
WO2013138121A1 (en) * 2012-03-16 2013-09-19 Cummins Inc. Aftertreatment system and method for pre-decomposed reductant solution
US8844269B2 (en) 2012-03-16 2014-09-30 Cummins Inc. Aftertreatment system and method for pre-decomposed reductant solution
JPWO2013153606A1 (en) * 2012-04-09 2015-12-17 トヨタ自動車株式会社 Exhaust gas purification device for internal combustion engine
US9561470B2 (en) 2014-02-14 2017-02-07 Deutz Aktiengesellschaft Method for the purification of diesel engine exhaust gases
US20170058738A1 (en) * 2015-08-28 2017-03-02 General Electric Company Treatment of emissions in power plants
US20180363527A1 (en) * 2017-06-16 2018-12-20 Watlow Electric Manufacturing Company Temperature-based control of reagent distribution
CN110741141A (en) * 2017-06-16 2020-01-31 沃特洛电气制造公司 Temperature-based control of reagent distribution
US11047281B2 (en) * 2017-06-16 2021-06-29 Watlow Electric Manufacturing Company Temperature-based control of reagent distribution
EP4089267A1 (en) * 2017-06-16 2022-11-16 Watlow Electric Manufacturing Company Temperature-based control of reagent distribution
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US11174772B2 (en) 2020-02-25 2021-11-16 Caterpillar Inc. Mitigation of diesel emission fluid (DEF) deposition in exhaust system for engine
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