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The use of alternative fuels, especially oxygenated fuels in automobile engines, has been increasing owing to the stringent global fuel economy and emission regulations. As a result, it is concerned that the emissions of alcohols and aldehydes have increased significantly. Aldehydes, formaldehyde (HCHO) in particular, are non-criteria pollutants that are acutely toxic and/or carcinogenic. Several reports have associated HCHO with potential lung and airway cancers. Therefore, emission regulations for these compounds have already been implemented in several areas worldwide. The conventional measurement (impinger, etc.) methods for HCHO possess advantages and disadvantages. HCHO can be measured with high sensitivity if measured in a batch. However, in real-time measurements, low concentration measurements are challenging.

Understanding the chemical reactions taking place in the engine and after-treatment systems is indispensable for minimizing harmful emissions in automotive exhaust gas. Real time gas analyzers for engine exhaust play a vital role for developing mathematical models and evaluating new after-treatment technologies. Gas analyzers using Fourier Transform Infrared Spectroscopy (FTIR) offer the advantage of continuous non-destructive simultaneous multicomponent analysis of a single gas stream. The ability of such analyzers to detect concentration fluctuations in the sample gas depends on a balance between its sample gas replacement rate and data sampling frequency. Increasing the sampling frequency is useful for detecting rapid concentration fluctuations, provided that the sample gas replacement rate is fast enough. This is commonly achieved by increasing the sample flow rate.

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.

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 coherent lights in the Mid-infrared (Mid-IR) region where these nitrogen compounds exhibit strong absorption tendency. Therefore, it is possible to detect very low concentration gas. QCL can also give a super fine resolution of the spectrum in this region. Therefore, utilization of this spectrometer can reduce the interference caused by the spectral overlap of coexisting gases in automobile engine exhaust. In the previous study, the fundamental concept of development along with some basic performance of the analyzer had been reported. In this study, improvement of performance has been attempted. Especially, the cell design, response time of NH₃, broadening the measurement ranges, and increasing the data sampling speed have been considered.

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.