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Diesel engine ash emissions are composed of the non-combustible portions of diesel particulate matter derived mainly from lube oil, and over time can degrade diesel particulate filter performance. This paper presents results from a high temperature oxidation method (HTOM) used to estimate ash emissions, and engine oil consumption in real-time. Atomized lubrication oil and diesel engine exhaust were used to evaluate the HTOM performance. Atomized fresh and used lube oil experiments showed that the HTOM reached stable particle size distributions and concentrations at temperatures above 700°C. The HTOM produced very similar number and volume weighted particle size distributions for both types of lube oils. The particle number size distribution was unimodal, with a geometric mean diameter of about 23 nm. The volume size distribution had a geometric volume mean diameter of about 65 nm.

Diesel low temperature combustion (LTC) is an operational strategy that is effective at reducing soot and oxides of Nitrogen (NOx) emissions at low engine loads in-cylinder. A downside to LTC in diesel engines is increased hydrocarbon (HC) emissions. This study shows that semi-volatile species from LTC form the bulk of particulate matter (PM) upon dilution in the atmosphere. The nature of gas-to-particle conversion from high HC operating modes like LTC has not been well characterized. In this work, we explore engine-out PM and HC emissions from LTC and conventional diffusion combustion (CC) operation for two different engine load and speed modes using a modern light-duty diesel engine. An experimental method to investigate PM volatility was implemented. Raw exhaust was diluted under two dilution conditions. A tandem differential mobility analyzer (TDMA) was used to identify differences in volatility between particle sizes.

Diesel low temperature combustion (LTC) is an operational strategy that effectively limits soot and oxides of nitrogen (NOx) emissions in-cylinder. Unfortunately, LTC results in increased hydrocarbon emissions as compared to conventional diesel combustion (CDC). Previous work has shown that exhaust conditions resulting from LTC inhibit oxidation of HC within a diesel oxidation catalyst (DOC). Further, these elevated HC emissions result in engine-out particulate matter (PM) that primarily consists of semi-volatile organic material. The current work shows that a DOC incompletely oxidizes this PM forming material. These results investigated the effectiveness of both a DOC and a diesel particulate filter (DPF) in reducing particle emissions for LTC. In this work, engine-out, DOC-out, and DPF-out exhaust were sampled using a micro-dilution system. Particle distributions were determined with a scanning mobility particle sizer (SMPS) and engine exhaust particle sizer (EEPS).

The objective of this work is to improve the understanding of variables like dilution and sampling conditions that contribute to particle-based emission measurements by assessing and comparing the nucleation tendency of diesel aerosols when diluted with a porous wall dilutor or an air ejector in a laboratory setting. An air-ejector dilutor and typical dilution conditions were used to establish the baseline sensitivity to dilution conditions for the given engine operating condition. A porous tube dilutor was designed and special attention was given to integrating the dilutor with the exhaust pipe and residence time chamber. Results from this system were compared with the ejector dilutor. Exhaust aerosols were generated by a Deere 4045 diesel engine running at low speed (1400 rpm) and low load (50 Nm, ~10% of rated). Primary dilution parameters that were varied included dilution air temperature (25 and 47°C) and dilution ratio (5, 14, and 55).

The European Emissions Stage 5b standard for diesel passenger cars regulates particulate matter to 0.0045 g/km and non-volatile part/km greater than 23 nm size to 6.0x10₁₁ as determined by the PMP procedure that uses a heated evaporation tube to remove semi-volatile material. Measurement artifacts associated with the evaporation tube technique prevents reliable extension of the method to a lower size range. Catalytic stripper (CS) technology removes possible sources of these artifacts by effectively removing all hydrocarbons and sulfuric acid in the gas phase in order to avoid any chemical reactions or re-nucleation that may cause measurement complications. The performance of a miniature CS was evaluated and experimental results showed solid particle penetration was 50% at 10.5 nm. The sulfate storage capacity integrated into the CS enabled it to chemically remove sulfuric acid vapor rather than rely on dilution to prevent nucleation.

Combustion aerosols consist mainly of elemental and organic carbon (EC and OC). Since EC strongly absorbs light and thus affects atmospheric visibility and radiation balance, there is great interest in its measurement. To this end, the National Institute for Occupational Safety and Health (NIOSH) published a standard method to determine the mass of EC and OC on filter samples. Another common method of measuring carbon in aerosols is the aethalometer, which uses light extinction to measure “black carbon” or BC, which is considered to approximate EC. A third method sometimes used for estimating carbon in submicron combustion aerosols, is to measure particle size distributions using a scanning mobility particle sizer (SMPS) and calculate mass using the assumptions that the particles are spherical, carbonaceous and of known density.

The effects of fuel sulfur content and dilution conditions on diesel engine PM number emissions have been researched extensively through steady state testing. Most results show that the concentration of nuclei-mode particles emitted increases with fuel sulfur content. A few studies further observed that fuel sulfur content has little effect on the emissions of heavily-used engines. It has also been found that primary dilution conditions can have a large impact on the size and number distribution of the nuclei-mode particles. These effects, however, have not yet been fully understood through transient testing, the method used by governments worldwide to certify engines and regulate emissions, and a means of experimentation which generates realistic conditions of on-road vehicles by varying the load and speed of the engine.

Earlier work [1] shows that kinetics of Diesel soot oxidation is different from that of ethylene diffusion flame soot oxidation [2], possibly due to metals from lube oil. This study investigates the influence of metals on soot oxidation and the exhaust particle emissions using lube oil dosed fuel (2 % by volume). This method does not simulate normal lube oil consumption, but is used as a means of adding metals to particles for oxidation studies. This study also provides insight into the effect of systems that mix lube oil with fuel to minimize oil change service. The HTO-TDMA (High Temperature Oxidation-Tandem Differential Mobility Analyzer) technique [1] was used to measure the surface specific oxidation rate of Diesel particles over the temperature range 500-750 °C. Diesel particles sampled from the exhaust stream of a Diesel engine were size segregated by differential mobility and oxidized in situ in air in a heated flow tube of known residence time and temperature profile.

A one-stage dilution tunnel has been developed to sample and dilute diesel exhaust. The tunnel has the capability of simulating many aspects of the atmospheric dilution process. The dilution rate and overall dilution ratio, temperature, relative humidity, and residence time in the tunnel, as well as residence time and temperature in the transfer line between the tunnel and exhaust sampling point may be varied. In this work we studied the influence of the exhaust transfer line, tunnel residence time, and dilution air temperature on the exhaust particle size distribution. The influences of fuel sulfur content on the size distribution and on the sensitivity of the size distribution to dilution and sampling conditions were also examined. We do not suggest an optimum dilution scheme, but do identify critical variables.

This study investigates the combustion and emissions of a compression ignition (CI) engine operating with mixtures of hydrogen (H₂) and carbon monoxide (CO) injected with the intake air. Hydrogen and carbon monoxide were chosen as the gaseous fuels, because they represent the main fuel component of synthesis gas, which can be produced by a variety of methods and feed stocks. However, due to varying feed stock and production mechanisms, syngas composition can vary significantly. It is currently unknown how a varying H₂/CO (syngas) ratio affects the cycle efficiency and gaseous emissions. The experiments were performed on an air-cooled, naturally aspirated, direct injection diesel engine. The engine was operated at 1800 RPM with a compression ratio of 21.2:1. Two load conditions were tested; 2 bar and 4 bar net indicated mean effective pressure (IMEPⁿ). For all test conditions the added syngas demonstrated lower cycle efficiency than the diesel fuel baseline.

Four-way, integrated, diesel emission control systems that combine selective catalytic reduction for NOx control with a continuously regenerating trap to remove diesel particulate matter were evaluated under real-world, on-road conditions. Tests were conducted using a semi-tractor with an emissions year 2000, 6-cylinder, 12 L, Volvo engine rated at 287 kW at 1800 rpm and 1964 N-m. The emission control system was certified for retrofit application on-highway trucks, model years 1994 through 2002, with 4-stroke, 186-373 kW (250-500 hp) heavy-duty diesel engines without exhaust gas recirculation. The evaluations were unique because the mobile laboratory platform enabled evaluation under real-world exhaust plume dilution conditions as opposed to laboratory dilution conditions. Real-time plume measurements for NOx, particle number concentration and size distribution were made and emission control performance was evaluated on-road.

Nanoparticle formation during exhaust sampling and dilution has been examined using a two-stage micro-dilution system to sample the exhaust from a modern, medium-duty diesel engine. Growth rates of nanoparticles at different exhaust dilution ratios and temperatures have been determined by monitoring the evolution of particle size distributions in the first stage of the dilution system. Two methods, graphical and analytical, are described to determine particle growth rate. Extrapolation of size distribution down to 1 nm in diameter has been demonstrated using the graphical method. The average growth rate of nanoparticles is calculated using the analytical method. The growth rate ranges from 6 nm/sec to 24 nm/sec, except at a dilution ratio of 40 and primary dilution temperature of 48 °C where the growth rate drops to 2 nm /sec. This condition seems to represent a threshold for growth. Observed nucleation and growth patterns are consistent with predictions of a simple physical model.