Photoacoustic Detection of Pollutants Emitted by Transportation System for Use in Automotive Industry

In photoacoustic spectroscopy, the signal is inversely proportional to the resonant cell volume. Photoacoustic spectroscopy (PAS) is an absorption spectroscopy technique that is suitable for detecting gases at low concentrations. This desirable feature has created a growing interest in miniaturizing...

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Veröffentlicht in:Photonics 2022-08, Vol.9 (8), p.526
Hauptverfasser: Vafaie, Reza Hadjiaghaie, Pour, Roya Shafiei, Mohammadzadeh, Ardashir, Asad, Jihad H., Mosavi, Amir
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Sprache:eng
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Zusammenfassung:In photoacoustic spectroscopy, the signal is inversely proportional to the resonant cell volume. Photoacoustic spectroscopy (PAS) is an absorption spectroscopy technique that is suitable for detecting gases at low concentrations. This desirable feature has created a growing interest in miniaturizing PA cells in recent years. In this paper, a simulation of a miniaturized H-type photoacoustic cell consisting of two buffer holes and a resonator was performed in order to detect CO, NH3, NO, and CH4 pollutants. These gases are the main components of the air pollutants that are produced by the automotive industry. The linear forms of the continuity, Navier–Stokes equations, and the energy equation were solved using the finite element method in a gaseous medium. The generated pressure could be measured by a MEMS sensor. Photoacoustic spectroscopy has proven to be a sensitive method for detecting pollutant gases. The objectives of the measurements were: determining the proper position of the pressure gauge sensor; measuring the frequency response; measuring the frequency response changes at different temperatures; studying the local velocity at the resonant frequency; and calculating the quality factor. The acoustic quality coefficient, acoustic response (pressure), local velocity, frequency response, and the effect of different temperatures on the frequency response were investigated. A frequency response measurement represents the fact that different gases have different resonance frequencies, for which CO and NO gases had values of 23.131 kHz and 23.329 kHz, respectively. The difference between these gases was 200 Hz. NH3 and CH4 gases with values of 21.206 kHz and 21.106 kHz were separable with a difference of 100 Hz. In addition, CO and NO gases had a difference of 2000 Hz compared to NH3 and CH4, which indicates the characteristic fingerprint of the designed cell in the detection of different gases. Better access to high-frequency acoustic signals was the goal of the presented model in this paper.
ISSN:2304-6732
2304-6732
DOI:10.3390/photonics9080526