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This paper describes the joint development by Tenneco and Pi Shurlok of a complete diesel engine aftertreatment system for controlling particulate matter emissions. The system consists of a DOC, DPF, sensors, controller and an exhaust fuel injection system to allow active DPF regeneration. The mechanical components were designed for flow uniformity, low backpressure and component durability. The overall package is intended as a complete PM control system solution for OEMs, which does not require any significant additions to the OEM's engine control strategies and minimizes integration complexity. Thus, to make it easier to adapt to different engine platforms, ranging from small off-road vehicle engines to large locomotive engines, model-based control algorithms were developed in preference to map-based controls.

Catalysts and filters continue to be applied widely to meet particulate matter regulations across new and retrofit diesel engines. Soot management of the filter continues to be enhanced, including regeneration methodologies. Concerns regarding in-cylinder post-injection of fuel for active regeneration increases interests in directly injecting this fuel into the exhaust. Performance of secondary fuel injection layouts is discussed, and sensitivities on thermal uniformity are measured and analyzed, providing insight to packaging challenges and methods to characterize and improve application designs. Influences of end cone geometries, mixers, and injector mounting positions are quantified via thermal distribution at each substrate's outlet. A flow laboratory is applied for steady state characterization, repeated on an engine dynamometer, which also provides transient results across the NRTC.

Evolving marine diesel emission regulations drive significant reductions of nitrogen oxide (NOx) emissions. There is, therefore, considerable interest to develop and validate Selective Catalytic Reduction (SCR) converters for marine diesel NOx emission control. Substrates in marine applications need to be robust to survive the high sulfur content of marine fuels and must offer cost and pressure drop benefits. In principle, extruded honeycomb substrates of higher cell density offer benefits on system volume and provide increased catalyst area (in direct trade-off with increased pressure drop). However higher cell densities may become more easily plugged by deposition of soot and/or sulfate particulates, on the inlet face of the monolithic converter, as well as on the channel walls and catalyst coating, eventually leading to unacceptable flow restriction or suppression of catalytic function.

Exhaust systems traditionally require a specific amount of muffler volume to reduce sound levels appropriately. However, as hybridization evolves, the packaging area becomes smaller, reducing available muffler space and requiring alternative solutions to attenuate exhaust sound with less volume. Passive exhaust valves are a key solution, leveraging the physics of the exhaust (flow, temperature, and pressure) to cycle the valve. Passive exhaust valves typically operate in a closed position under low-flow conditions (low engine speeds and loads), which helps to reduce low-frequency boom, moderately increasing backpressure when it is not detrimental to engine efficiency. Conversely, under higher engine speed and load operating conditions, when exhaust flow increases and backpressure is critical to achieve desired power output, the passive valve opens to reduce its impact.

EPA 2015 Tier IV emission requirements pose significant challenges to large diesel engine aftertreatment system (EAS) development aimed at reducing exhaust emissions such as NOx and PM. An EAS has three primary subsystems, Aftertreatment hardware, controls and fluid delivery. Fluid delivery is the subsystem which supplies urea into exhaust stream to allow SCR catalytic reaction and/or periodic DOC diesel dosing to elevate exhaust temperatures for diesel particulate filter (DPF) soot regeneration. The purpose of this paper is to discuss various aspects of fluid delivery system development from flow and pressure perspective. It starts by giving an overview of the system requirements and outlining theoretical background; then discusses overall design considerations, injector and pump selection criteria, and three main injector layouts. Steady state system performance was studied for manifold layout.

As Selective Catalytic Reduction (SCR) NOx abatement systems gain commercial acceptance and popularity, the need for efficiency predictive capabilities increases. To this end, a flow bench was developed capable of varying steady state inputs (temperature, flow rate and NOx concentration). The efficiencies of various SCR systems was measured and compared. This concept of a steady state flow bench approach allows for an efficient and cost effective means to evaluate comparable system designs.

Future LEV-III tailpipe (TP) emission regulations pose an enormous challenge forcing the fleet average of light-duty vehicles produced in the 2025 model year to perform at the super ultralow emission vehicle (SULEV-30) certification levels (versus less than 20% produced today). To achieve SULEV-30, regulated TP emissions of non-methane organic gas (NMOG) hydrocarbons (HCs) and oxygenates plus oxides of nitrogen (NOx) must be below a combined 30 mg/mi (18.6 mg/km) standard as measured on the federal emissions certification cycle (FTP-75). However, when flex-fuel vehicles use E85 fuel instead of gasoline, NMOG emissions at cold start are nearly doubled, before the catalytic converter is active. Passive HC traps (HCTs) are a potential solution to reduce TP NMOG emissions. The conventional HCT design was modified by changing the zeolite chemistry so as to improve HC retention coupled with more efficient combustion during the desorption phase.

In the development of HC traps (HCT) for reducing vehicle cold start hydrocarbon (HC)/nitrogen oxide (NOx) emissions, zeolite-based adsorbent materials were studied as key components for the capture and release of the main gasoline-type HC/NOx species in the vehicle exhaust gas. Typical zeolite materials capture and release certain HC and NOx species at low temperatures (<200°C), which is lower than the light-off temperature of a typical three-way catalyst (TWC) (≥250°C). Therefore, a zeolite alone is not effective in enhancing cold start HC/NOx emission control. We have found that a small amount of Pd (<0.5 wt%) dispersed in the zeolite (i.e., BEA) can significantly increase the conversion efficiency of certain HC/NOx species by increasing their release temperature. Pd was also found to modify the adsorption process from pure physisorption to chemisorption and may have played a role in the transformation of the adsorbed HCs to higher molecular weight species.

Passive in-line catalyzed hydrocarbon (HC) traps have been used by some manufacturers in the automotive industry to reduce regulated tailpipe (TP) emissions of non-methane organic gas (NMOG) during engine cold-start conditions. However, most NMOG molecules produced during gasoline combustion are only weakly adsorbed via physisorption onto the zeolites typically used in a HC trap. As a consequence, NMOG desorption occurs at low temperatures resulting in the use of very high platinum group metal (PGM) loadings in an effort to combust NMOG before it escapes from a HC trap. In the current study, a 2.0 L direct-injection (DI) Ford Focus running on gasoline fuel was evaluated with full useful life aftertreatment where the underbody converter was either a three-way catalyst (TWC) or a HC trap. A new HC trap technology developed by Ford and Umicore demonstrated reduced TP NMOG emissions of 50% over the TWC-only system without any increase in oxides of oxygen (NOx) emissions.

With stricter emissions standards, low back pressure requirements, and 100,000 mile durability specifications, ceramic catalysts have undergone significant developments over the past few years. The thrust in the ceramics area has centered on thin-wall structures to minimize back pressure and on high cell density for rapid light-off in close-coupled applications. The thin-wall structures are extruded from low expansion cordierite ceramic with adequate strength and thermal shock resistance equivalent to those of standard cordierite substrate. Examples of thin-wall substrate include 350XT which is extruded from a very low expansion dense cordierite ceramic, and 400/4 and 600/4 cell structures extruded from a low expansion modified cordierite ceramic. This paper will focus on the high fatigue resistance, excellent conversion efficiency, and low back pressure of 350 XT substrates with advanced washcoat system.

Monolithic emission control devices typically use a support mat material to provide mechanical support, mechanical isolation, and thermal insulation for ceramic monoliths. This material is similar to a felt, but made from ceramic fibers. Non-intumescent support mat materials contain only ceramic fibers and binder compounds, while intumescent support mats also contain vermiculite; a material that expands with the application of heat. The durability of the support mat is critical to the durability of the overall emission control components. In addition to many component validation methods that evaluate the durability of the entire system methods to evaluate the response and predict the durability of the support mat itself help provide important design information. This paper summarizes challenges and artifacts in support mat testing.

2010 and future EPA regulations introduce stringent Oxides of Nitrogen (NOx) reduction targets for diesel engines. Selective Catalytic Reduction (SCR) of NOx by Urea over catalyst has become one of the main solutions to achieve these aggressive reductions. As such, urea solution is injected into the exhaust gas, evaporated and decomposed to ammonia via mixing with the hot exhaust gas before passing through an SCR catalyst. Urea mixers, in this regard, are crucial to ensure successful evaporation and mixing since its liquid state poses significant barriers, especially at low temperature conditions that incur undesired deposits. Intensive efforts have been taken toward developing such urea mixers, and multiple criteria have been derived for them, mainly including NOx reduction efficiency and uniformity. In addition, mixers must also satisfy other requirements such as low pressure drop penalty, mechanical strength, material integrity, low cost, and manufacturability.

An active diesel particulate filter (DPF) regeneration system is evaluated, which applies secondary fuel injection (SFI) directly within the exhaust system upstream of a diesel oxidation catalyst (DOC). Diesel fuel is oxidized in the presence of a proprietary catalyst system, increasing exhaust gas temperatures in an efficient and controlled manner, even during low engine-out gas temperatures. The exotherms produced by secondary fuel injection (SFI) have been evaluated using two different DOC volumes and platinum catalyst loadings. DOC light-off temperatures were measured using SFI under steady-state conditions on an engine dynamometer. A ΔT method was used for the light-off temperature measurements – i.e., the minimum DOC inlet gas temperature at which the exothermic reaction increases the outlet gas temperature 20°C or greater than the inlet temperature.

In order to satisfy tightening global emissions regulations, diesel truck manufacturers are striving to meet increasingly stringent Oxides of Nitrogen (NOx) reduction standards. The majority of heavy duty diesel trucks have integrated urea SCR NOx abatement strategies. To this end, aftertreatment systems need to be properly engineered to achieve high conversion efficiencies. A EuroV intent urea SCR system is evaluated and failed to meet NOx conversion targets with severe urea deposit formation. Systematic enhancements of the design have been performed to enable it to meet targets, including emission reduction efficiency via improved reagent mixing, evaporation, distribution, back pressure, and removing of urea deposits. Multiple urea mixers, injector mounting positions and various system layouts are developed and evaluated, including both CFD analysis and full scale laboratory tests.

With increasing applications of urea SCR for NOx emission reduction, improving the system performance and durability has become a high priority. A typical urea SCR system includes a urea injector, injector housing, mixer, and appropriate pipe configurations to allow continuous urea injection into the exhaust stream and evaporation of urea solution into gaseous products. Continuous operation at various conditions with high NOx reduction is possible, but one problem that threatens the life and performance of these systems is urea deposit. When urea or its byproducts become deposited on the inner surfaces of the system including walls, mixers, injector housings and substrates it can create concerns of backpressure and material deteriorations. In addition, deposits as a waste of reagents can negatively affect engine operation, emissions performance and DEF economy. Urea deposit behavior is explored in terms of heat transfer, pipe geometry, injector layout and mixing mechanisms.

The presented work evaluates several mixer designs being considered for use in large Diesel exhaust aftertreatment systems. The mixers are placed upstream of a diesel oxidation catalyst (DOC) in the exhaust system, where a liquid hydrocarbon fuel is injected. DOC exothermic behaviour resulting from each mixer at different operating conditions is evaluated. A gas flow bench equipped with a XY-Table measurement system is used to determine gas velocity, temperature, and hydrocarbon species uniformity, as well as, pressure drop. Experimental mixer data obtained from a flow bench and an engine dynamometer are compared and discussed. The experimental methodology used in this study can be used to evaluate mixers via comprehensive testing.

Diesel Particulate Filters (DPFs) have been successfully applied for several years to reduce Particulate Matter (PM) emissions from on-highway applications, and similar products are now also applied in off-highway markets and retrofit solutions. Most solutions are catalytically-based, necessitating minimum operating temperatures and demanding engine support strategies to reduce risks [1, 2, 3, 4, 5, 6, 7, 8]. An ignition-based thermal combustion device is applied with Cordierite and SiC filters, evaluating various DPF conditions, including effects of soot load, exhaust flow rates, catalytic coatings, and regeneration temperatures. System designs are described, including flow and temperature uniformity, as well as soot load distribution and thermal gradient response.

To meet EPA Tier IV large diesel engine emission targets, intensive development efforts are necessary to achieve NOx reduction and Particulate Matter (PM) reduction targets [1]. With respect to NOx reduction, liquid urea is typically used as the reagent to react with NOx via SCR catalyst [2]. Regarding to PM reduction, additional heat is required to raise exhaust temperature to reach DPF active / passive regeneration performance window [3]. Typically the heat can be generated by external diesel burners which allow diesel liquid droplets to react directly with oxygen in the exhaust gas [4]. Alternatively the heat can be generated by catalytic burners which enable diesel vapor to react with oxygen via DOC catalyst mostly through surface reactions [5].

Stringent global emissions legislations demand effective NOx reduction strategies for both the engine as well as the aftertreatment. Diesel applications have previously applied Lean NOx Catalysts (LNCs) [1, 2], but their reduction efficiency and longevity have been far less than that of the competing ammonia-based SCR systems, such as urea [3]. A catalyst has been developed to significantly reduce NOx emissions, approaching 60% with ULSD and exceeding 95% with E85. Both thermal and sulfur aging are applied, as well as on-engine aging, illustrating resilient performance to accommodate necessary life requirements. A robust system is developed to introduce both ULSD from the vehicle's tank as well as E85 (up to 85% ethanol with the balance being gasoline) from a moderately sized supplemental tank, enabling extended mileage service intervals to replenish the reductant, as compared with urea, particularly when coupled with an engine-out based NOx reduction technology, such as EGR.

Stringent global emissions legislation demands effective NOx reduction strategies, particularly for the aftertreatment, and current typical liquid urea SCR systems achieve efficiencies greater than 90% [1]. However, with such high-performing systems comes the trade-off of requiring a tank of reductant (urea water solution) to be filled regularly, usually as soon as the fuel fillings or as far as oil changes. Advantages of solid reductants, particularly ammonium carbamate, include greater ammonia densities, enabling the reductant refill interval to be extended several multiples versus a given reductant volume of urea, or diesel exhaust fluid (DEF) [2]. An additional advantage is direct gaseous ammonia dosing, enabling reductant injection at lower exhaust temperatures to widen its operational coverage achieving greater emissions reduction potential [3], as well as eliminating deposits, reducing mixing lengths, and avoiding freeze/thaw risks and investments.