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The US Code of Federal Regulations (CFR) Title 40 Part 1065 and 1066 require gravimetric determination of automobile Particulate Matter (PM) collected onto filter media from the diluted exhaust. PM is traditionally collected under simulated driving conditions in a laboratory from a full flow Constant Volume Sampler (CVS) system, where the total engine exhaust is diluted by HEPA filtered air. This conventional sampling and measurement practice is facing challenges in accurately quantifying PM at the upcoming 2025-2028 CARB LEVIII 1 mg/mi PM emissions standards. On the other hand, sampling a large amount of PM emitted from large size high power engines introduces additional challenges. Applying flow weighting, adjusting the Dilution Ratio (DR) and Filter Face Velocity (FFV) are proposed options to overcome these challenges.

Light-duty vehicle emission measurement test protocols defined in the Code of Federal Regulation (40 CFR Part 1066) allow sampling particulate matter (PM) of all phases of Federal Test Procedure (FTP-75) on a single PM sampling filter by means of flow-weighted sampling in order to increase PM mass loaded on the filter. A technical challenge is imposed especially for partial flow dilution systems (PFDS) to maintain a precise dilution ratio (DR) over such a wide sample flow range due to the subtraction flow determination method of dilution air and diluted exhaust flows, because the flow difference is critical at high DR conditions. In this study, an improved flow weighting concept is applied to a PFDS by installing a bypass line with a flow controller in parallel with the PM sampling filter in order to improve DR accuracy during flow-weighted sampling.

Automobile Particulate Matter (PM) Emission regulation requires gravimetric determination of PM collected on filter media under simulated driving conditions in the laboratory traditionally in a full flow Constant Volume Sampling (CVS) dilution tunnel. There have been discussions about whether current sampling and measurement practices are sufficiently accurate in quantifying PM at the upcoming 1mg/mi PM emissions standards of CARB LEV III. Sampling technique alternative to a CVS such as a Partial Flow Dilution (PFD) system has already been developed and is acceptable for certification testing. Lower dilution ratios and higher filter face velocity (FFV) are options to load traceable amount of PM on filter in case of light duty vehicle (LDV) testing. On the other hand higher dilution ratios and lower FFV are required for heavy duty engine (HDE) testing to keep the PM loaded on filter <400μg.

In the engine and vehicle test procedures described in Parts 1065/1066 of Title 40 of the Code of Federal Regulations (CFR), the United States Environmental Protection Agency (US-EPA) allows for the measurement of N2O emissions from sample storage bags, from a continuous dilute stream or a raw exhaust stream. Typically, batch (Bag) sampling has better accuracy and repeatability, but continuous sampling is more efficient in terms of test cell running time and provides test-mode emissions with good correlation to bag measurements. In this study, correlations between bag sampling and continuous dilute exhaust sampling were investigated using a fleet of vehicles with a wide range of N2O emission levels. Very good correlation between these two sampling methods was observed for the majority of tests conducted. In the best cases, differences in average N2O concentration levels measured by these two methods were less than +/− 1%.

Nitrous oxide (N₂O) emission reduction has gained large prominence recently due to its contribution to the climate change as a greenhouse gas. The United States Environment Protection Agency (US-EPA) together with the United States Department of Transport (DOT) has already regulated the N₂O emissions from light-duty vehicles (LDV) to 0.010 g/mile. For LDV, N₂O measurement should be done from sample storage bags over the light-duty FTP drive cycles. N₂O emission standard of 0.10 g/bhp-hr for heavy-duty engines (HDE) is also finalized. The final N₂O standard becomes effective in 2014 model year for diesel engines. Usually raw or diluted exhaust is measured for HDE emission testing. Therefore, an analyzer capable of measuring N₂O from bag and from diluted sample continuously is required to support both LDV and HDE regulations.

The United States Environmental Protection Agency (EPA) has finalized a reporting rule for the Greenhouse Gases (GHGs) emissions including Nitrous Oxide (N₂O) from all sectors of the economy. In addition, EPA and the National Highway Traffic Safety Administration (NHTSA) have been working together on developing a National Program of harmonized regulations to reduce GHGs emissions and improve fuel economy of light-duty vehicles (LDV). As a consequence, the limiting value for N₂O emission from LDV is set to 0.01 g/mile. Considering this regulatory limit of N₂O emission from LDV, if the exhaust gas is diluted and stored in a sample storage bag, the concentration of N₂O becomes very low which requires a highly sensitive analyzer for accurate measurement. In the previous study, an instrument based on Quantum Cascade Mid-IR Laser (QCL-Mid IR) Spectroscopy has been developed for measuring ultra-low level of N₂O in automobile exhaust gas sampled in a sample storage bag.

Green House Gas (GHGs) emission reduction has gained large prominence globally due to the climate change. Nitrous Oxide (N₂O) emission from transportation has significant share on global warming. Therefore, an instrument for sensing ultra-low level of N₂O is a key global demand. In this study, development of an instrument based on the Quantum Cascade Laser (QCL) has been attempted for measuring ultra-low level N₂O in automobile exhaust gas sampled in a sample storage bag. The QCL can emit coherent lights in a mid-infrared (Mid-IR) region where N₂O shows strong absorption peak. This absorption peak can be detected by an MCT (Mercury Cadmium Tellurium) type photovoltaic detector. The optics configuration used in this study can give a superfine resolution of the Mid-IR spectrum such as 0.002 cm-₁ in the target wavelength band. Therefore, utilizing this spectrometer, measurement of ultra-low level N₂O is possible without interference of co-existing gases.

An analyzer based on Quantum Cascade Laser (QCL) has been developed for chemical sensing of gaseous nitrogen compounds (NO, NO2, N2O and NH3). The QCL can emit lights in a mid-infrared (Mid-IR) region where these nitrogen compounds have strong absorption. This laser optics configuration can give a super fine resolution of the mid-infrared spectrum. Therefore, utilizing this spectrometer can reduce the interference caused by the spectral overlap of co-existing gases in engine exhaust. The developed analyzer has been evaluated using actual engine exhaust to confirm the influence from coexisting gases and the measurement accuracies and stabilities. Very low detection limit (less than 1 ppm) and quick response time (less than 2 sec) have been achieved even with the newly developed analyzer.

Monodisperse and polydisperse Sodium Chloride (NaCl) particles were used to calibrate the solid particle penetration for the Volatile Particle Remover (VPR) in a Horiba prototype Solid Particle Counting System (SPCS). Prior to the calibration, dilution ratios on the SPCS are verified carefully with a flame ionization analyzer (FIA). Size distributions for polydisperse aerosols upstream and downstream of the Volatile Particle Remover (VPR) were measured with a Scanning Mobility Particle Sizer (SMPS). It is found that overall penetrations for polydisperse aerosols are larger than 95%. Geometric standard deviations from the raw and the diluted by the VPR are within ±1.5% difference. Thus, shapes of size distributions aren't changed after dilution. Geometric mean diameters shift a little, on average ±5% after dilution. Therefore, the VPR doesn't change the aerosol characteristics after the aerosol is diluted and heated up to 320 °C.

A Solid Particle Counting System (SPCS) has been developed according to the ECE draft regulation proposed by the particle measurement program (PMP). In the previous report the basic performance of the SPCS has been mentioned in detail [1, 2, 3, 4, 5 and 6]. It has been reported that the SPCS demonstrates very stable dilution of sample with air and the error of real time dilution factor is less than 6% up to the total dilution factor of 1000. Penetration of solid particles through the SPCS is over 95% and volatile particles removal efficiency is over 99%. In this study the SPCS has been used to investigate the soot emission behavior from different vehicles with different after-treatment technologies. Direct injection (DI) diesel vehicles without diesel particulate filter (DPF), and with different DPFs (catalyzed and non-catalyzed) have been tested. Direct injection gasoline (DIG) vehicle with oxidation and NOx reduction catalysts have also been tested.

The prototype solid particle counting system (SPCS) has been used to study solid particle emission from gasoline and diesel vehicles. As recommended by the PMP draft proposal, exhaust is diluted by a Constant Volume Sampler (CVS). The SPCS takes the sample from the CVS tunnel. Transient test cycles such as EPA FTP 75, EPA HWFET (EPA Highway Fuel Economy Cycle), and NEDC (New European Driving Cycle) were tested. The repeatability of the instrument was evaluated on the diesel vehicle for three continuous days. The instrument exhibits good repeatability. The differences for the EPA ftp 75, the EPA HWFET, and the NEDC in three continuous tests are ± 3.5%. The instrument is very sensitive as well and detects the driving differences. A large number of solid particles are found during the hard acceleration from both the gasoline and the diesel vehicles. Solid particle emissions decrease quickly at deceleration and when vehicles approach constant speed.

A prototype solid particle counting system (SPCS) has been developed in Horiba. It measures the engine exhaust solid particle number emissions in real-time. The instrument is designed to follow the recommendation in the PMP proposal for solid particle number emissions measurement on Light-duty diesel vehicles. Two wide range continuous diluters, which were developed during this project, have been used as cold and hot diluters, respectively. The accuracy of the dilution ratio is normally ± 4% for the designed range. The instrument has low particle losses, and exhibits over 95% penetration for solid particles. The new instrument has functions such as, normal measurement, dilution ratio control, daily calibration for condensation particle counter (CPC), etc. These functions have been automated to make the instrument's operation simple.

Conditioning of diluted exhaust gas by Thermo-Conditioner prior to measurement has been proposed by the GRPE/PMP Research Council of the United Nation in order to achieve stability in nano-particle measurement. In this study the effect of thermo-conditioner on the thermo-physical behavior of nano-particle under different conditions have been clarified. Stability in measurement was also attempted depending on the characteristics of nano-particles. Quality of the raw exhaust gas, the dilution ratio and temperature, and the thermal conditioning temperature were considered as the main parameters. Exhaust gas from a medium duty DI diesel engine was used for analysis. Scanning Mobility Particle Sizer was used for measuring the concentration of nano-particles. It was concluded that the concentration of nuclei-mode particles within the size range of 15∼30 nm are significantly influenced by the thermal conditioning temperature.

In the previous study design of two-component normal paraffin fuel was attempted considering the components and blending ratio. Only the thermodynamic analysis of combustion and analysis of emission characteristics were performed to evaluate the design performance. In this study mixture formation behavior and combustion phenomena of pure and mixed n-paraffin fuels were investigated by direct visualization in an AVL engine with bottom view piston. The experiments included laser-illuminated high-speed photography of the fuel injection phase and combustion phase to investigate physical differences. The results obtained for the proposed fuels are compared with the results of conventional diesel fuel. It was found that the two component normal paraffin fuels with similar thermo physical properties have very similar spray development pattern but evaporation rates are different.

Fuel formulation for premixed charge compression ignition (PCCI) combustion has been attempted based on the mixture formation and auto-ignition behavior of normal paraffin fuels. Different pure and mixed fuels with different blending ratios are tested. The mixture formation behavior is investigated photographically in a constant volume combustion chamber (CVCC) at elevated temperature and pressure. Auto-ignition behavior is tested in a Fuel Ignition Analyzer under different test conditions. It is found that the evaporation rate of pure n-paraffin fuel increases and the ignition delay becomes longer with decreases in the chain length. In the range of test condition used in this study, the flash-boiling phenomenon affects the fuel evaporation rate and ignition delay to some extent. Based on the experimental results a mixture of a very light mixture promoting component (MPC) and a moderately dense igniting component (IC) at a ratio of 3:1 is found to be optimum for PCCI combustion.

The effect of boiling point difference as well as the flash boiling of two-component normal paraffin fuels on combustion and exhaust emission has been examined under different test conditions. To obtain a wide variation in boiling point between components different high boiling point fuels (n-undecane, n-tridecane and n-hexadecane) were blended with a low boiling point fuel (n-pentane) and different low boiling point fuels (n-pentane, n-hexane, and n-heptane) were blended with a high boiling point fuel (n-hexadecane). In addition the volume fraction of n-pentane was varied to have the best mixture ratio with n-tridecane. These fuel combinations exhibit different potential for flash boiling based on a certain ambient condition. The results indicate that though the potential for flash boiling is the highest for a mixture of n-pentane and n-hexadecane it emits about 20% higher PM than a mixture of n-pentane and n-tridecane.

This study proposes a new combustion chamber concept for small DI diesel engines. Reduction of fuel adhering to the cavity wall, improvements in mixture formation, and an optimum distribution of mixture inside and outside the cavity are the main characteristics of the combustion chamber. The spray formation and it's distribution inside and outside the combustion chamber was investigated photographically in a small DI diesel engine with transparent cylinder and piston. Optimization of the fuel spray distribution inside and outside the cavity was attempted by changing the shape of the cavity entrance and the location where spray impinges on the lip. In addition improvements in the mixture formation of the impinging spray and reductions in the fuel adhering to the cavity wall were attempted by introducing a small step on the cavity side wall. The results were confirmed by analyzing the combustion and emission in an actual DI diesel engine.

Modern small DI diesel engines are operated at high loads and high speeds. In these engines the spray spreading on the cavity walls during the main combustion is kept approximately constant at all engine speeds to optimize the air utilization. However, spray spreading on the wall during the early and late part of combustion changes with engine speed due to the changes in air motion. At the end of impingement much of the spray moves outside the cavity due to a strong reverse squish when the injection timing is set near TDC. This causes incomplete combustion of fuel and increase emissions of HC and soot. Therefore, the study of the behavior of spray affected by the reverse squish is very important. In this study the fuel spray development under high injection pressure and high gas charging pressure was investigated photographically in a small direct injection diesel engine with a common rail injection system.

Direct injection diesel engines emit a far more disagreeable exhaust odor at idling than gasoline engines, and with increasing numbers of DI diesel engines in passenger cars, it is important to promote the odor reduction research. High pressure injection in DI diesel engines promotes combustion and decreases particulate matter (PM) emissions, but injection pressures at idling and warm up are limited to 30∼40 MPa considering engine noise and vibration. In this pressure range, a part of the fuel adheres on the relatively cool combustion chamber walls and causes incomplete combustion, producing higher concentration of unburned HC and intermediate combustion components (aldehydes, other oxygenated compounds, etc.) with objectionable exhaust odors. To reduce the exhaust odor, oxidation catalysts are effective, but catalyst activity is poor at idling, when the exhaust gas temperature is low (about 100°C).