Multivariate-coupled-enhanced photoacoustic spectroscopy with Chebyshev rational fractional-order filtering algorithm for trace CH4 detection

An innovative and miniature photoacoustic spectroscopy (PAS) gas sensor based on a multivariate-coupled amplification photoacoustic cell (MVCA-PAC) with a total length of 100 mm was developed to achieve ultra-sensitive trace CH4 detection. Acoustic pressure distribution simulations reveal that at th...

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Published inPhotoacoustics (Munich) Vol. 42; p. 100692
Main Authors Zha, Shenlong, Chen, Hang, Liu, Chen, Guo, Yuxiang, Ma, Hongliang, Zhang, Qilei, Li, Lingli, Zhan, Shengbao, Cheng, Gang, Cao, Yanan, Pan, Pan
Format Journal Article
LanguageEnglish
Published Elsevier GmbH 01.04.2025
Elsevier
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ISSN2213-5979
2213-5979
DOI10.1016/j.pacs.2025.100692

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Summary:An innovative and miniature photoacoustic spectroscopy (PAS) gas sensor based on a multivariate-coupled amplification photoacoustic cell (MVCA-PAC) with a total length of 100 mm was developed to achieve ultra-sensitive trace CH4 detection. Acoustic pressure distribution simulations reveal that at the first-order resonance frequency, the MVCA-PAC achieves a maximum acoustic pressure approximately 3.9 times higher than that of a conventional photoacoustic cell. The absorption optical path of the MVCA-PAC reached 2068 mm through 22 reflections, resulting in a 2-fold increase in the amplitude of photoacoustic signals compared to the traditional photoacoustic cell with an equivalent absorption optical path. Furthermore, compared to a single-pass photoacoustic cell, the 2-f signal intensity of the MVCA-PAC increased by a factor of 4.5. Allan variance analysis indicated a detection limit of 0.572 ppm for CH4 detection with an averaging time of approximately 300 s. To further improve the measurement precision of the designed sensor, the Chebyshev rational fractional-order filtering (CRFOF) algorithm was introduced for PAS signal processing for the first time. Post-processing results demonstrated a 15.4-fold improvement in measurement precision, achieving a precision of 0.578 ppm. Finally, continuous monitoring of atmospheric CH4 over a 48-hour period validated the reliability and feasibility of the sensor.
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ISSN:2213-5979
2213-5979
DOI:10.1016/j.pacs.2025.100692