Fiber-Coupled Quartz-Enhanced Photoacoustic Spectroscopy System for Methane and Ethane Monitoring in the Near-Infrared Spectral Range

We report on a fiber-coupled, quartz-enhanced photoacoustic spectroscopy (QEPAS) near-IR sensor for sequential detection of methane (CH4 or C1) and ethane (C2H6 or C2) in air. With the aim of developing a lightweight, compact, low-power-consumption sensor suitable for unmanned aerial vehicles (UAVs)-empowered environmental monitoring, an all-fiber configuration was designed and realized. Two laser diodes emitting at 1653.7 nm and 1684 nm for CH4 and C2H6 detection, respectively, were fiber-combined and fiber-coupled to the collimator port of the acoustic detection module. No cross talk between methane and ethane QEPAS signal was observed, and the related peak signals were well resolved. The QEPAS sensor was calibrated using gas samples generated from certified concentrations of 1% CH4 in N2 and 1% C2H6 in N2. At a lock-in integration time of 100 ms, minimum detection limits of 0.76 ppm and 34 ppm for methane and ethane were achieved, respectively. The relaxation rate of CH4 in standard air has been investigated considering the effects of H2O, N2 and O2 molecules. No influence on the CH4 QEPAS signal is expected when the water vapor concentration level present in air varies in the range 0.6–3%.

Environmental Monitoring of Methane with Quartz-Enhanced Photoacoustic Spectroscopy Exploiting an Electronic Hygrometer to Compensate the H2O Influence on the Sensor Signal

A dual-gas sensor based on the combination of a quartz-enhanced photoacoustic spectroscopy (QEPAS) sensor and an electronic hygrometer was realized for the simultaneous detection of methane (CH4) and water vapor (H2O) in air. The QEPAS sensor employed an interband cascade laser operating at 3.34 μm capable of targeting a CH4 absorption line at 2988.8 cm−1 and a water line at 2988.6 cm−1. Water vapor was measured with both the electronic hygrometer and the QEPAS sensor for comparison. The measurement accuracy provided by the hygrometer enabled the adjustment of methane QEPAS signal with respect to the water vapor concentration to retrieve the actual CH4 concentration. The sensor was tested by performing prolonged measurements of CH4 and H2O over 60 h to demonstrate the effectiveness of this approach for environmental monitoring applications.

Quartz Enhanced Photoacoustic Detection Based on an Elliptical Laser Beam

A quartz enhanced photoacoustic spectroscopy (QEPAS) sensor system based on an elliptical laser beam for trace gas detection was demonstrated. A Powell lens was exploited to shape the circular laser beam into an elliptical laser beam for the full utilization of the quartz tuning fork (QTF) prong spacing. Based on the finite element modeling (FEM) simulation software COMSOL, the distribution of acoustic pressure on QTF prongs with different beam shapes was simulated theoretically. The experimental results showed that the QEPAS signal based on the elliptical laser beam had a 1.4-fold improvement compared with the circular laser beam, resulting in a minimum detection limit of 418.6 ppmv and the normalized noise equivalent absorption (NNEA) of 1.51 × 10−6 cm−1 W/√Hz at atmospheric pressure.

Trace Gas Detection System Based on All-Optical Quartz-Enhanced Photoacoustic Spectroscopy

An all-optical quartz-enhanced photoacoustic spectroscopy system (QEPAS) with quadrature point stabilization for trace gas detection was reported. The extrinsic interferometry-based optical fiber Fabry–Perot sensor with quadrature point self-stabilization for detection of quartz prong vibration was used to replace the conventional one. The optimal coefficient of the modulation depth was ∼2.2 theoretically and experimentally, corresponding to the modulation depth of ∼0.1795 cm−1 at an acetylene (C2H2) absorption line of 6534.36 cm−1. Furthermore, the enhancement of QEPAS signal was obtained by using different microresonators. The minimum detectable limit of ∼580 parts per billion by volume (ppbv) was obtained. A normalized noise equivalent absorption coefficient for C2H2 of 2.95 × 10−7 cm−1·W·Hz–1/2 was obtained. The detection sensitivity was enhanced by a factor of ∼2.1 in comparison to the conventional QEPAS system. The linear correlation coefficient of the QEPAS signal response to the C2H2 concentration was 0.998 within the range from 10 parts per million by volume (ppmv) to 500 ppmv. Finally, the long-term stability of the QEPAS system was evaluated using Allan deviation analysis, and the ultimate detection limit of ∼130 ppbv was reached for an optimum averaging time of ∼108 s at atmospheric pressure and ambient temperature.