Pressure sensing with two-color laser absorption spectroscopy for combustion diagnostics.

Pressure is an important parameter in assessing combustion performance that is typically measured using contact sensors. However, contact sensors usually disturb combustion flows and suffer from the temperature tolerance limit of sensor materials. In this Letter, an innovative noncontact two-color pressure sensing method based on tunable diode laser absorption spectroscopy (TDLAS) is proposed. This makes it possible to measure pressure at high temperature environments for combustion diagnostics. The proposed method uses the linear combination of the collision-broadened linewidths of two H2O absorption lines near 1343 and 1392 nm to measure the pressure. The feasibility and performance of such method have been demonstrated by measuring pressures from 1 to 5 bars at temperatures up to 1300 K with a laser wavelength scanning rate of 20 kHz. Measurement errors were found to be within 3%. Compared to previously reported TDLAS pressure sensors, this method is free from the influence of concentration and can also be combined with the existing two-color TDLAS thermometry to realize a fast, on line, and multi-parameter measurement in combustion diagnostics.

Portable TDLAS Sensor for Online Monitoring of CO2 and H2O Using a Miniaturized Multi-Pass Cell.

We designed a tunable diode laser absorption spectroscopy (TDLAS) sensor for the online monitoring of CO2 and H2O concentrations. It comprised a small self-design multi-pass cell, home-made laser drive circuits, and a data acquisition circuit. The optical and electrical parts and the gas circuit were integrated into a portable carrying case (height = 134 mm, length = 388 mm, and width = 290 mm). A TDLAS drive module (size: 90 mm × 45 mm) was designed to realize the function of laser current and temperature control with a temperature control accuracy of ±1.4 mK and a current control accuracy of ±0.5 µA, and signal acquisition and demodulation. The weight and power consumption of the TDLAS system were only 5 kg and 10 W, respectively. Distributed feedback lasers (2004 nm and 1392 nm) were employed to target CO2 and H2O absorption lines, respectively. According to Allan analysis, the detection limits of CO2 and H2O were 0.13 ppm and 3.7 ppm at an average time of 18 s and 35 s, respectively. The system response time was approximately 10 s. Sensor performance was verified by measuring atmospheric CO2 and H2O concentrations for 240 h. Experimental results were compared with those obtained using a commercial instrument LI-7500, which uses non-dispersive infrared technology. Measurements of the developed gas analyzer were in good agreement with those of the commercial instrument, and its accuracy was comparable. Therefore, the TDLAS sensor has strong application prospects in atmospheric CO2 and H2O concentration detection and ecological soil flux monitoring.

Double-enhanced multipass cell-based wavelength modulation spectroscopy CH4 sensor for ecological applications.

A novel CH4 sensor based on wavelength modulation spectroscopy with a multipass cell was developed for the soil respiration measurement of CH4. A home-made double-enhanced Herriot-type multipass cell with an effective absorption length of 73.926 m and a fiber-coupled distributed feedback diode laser emission at 1653.74 nm were used to design the sensor. The double enhancement of the effective optical pathlength of the multipass cell, absorption line locking, laser intensity normalization, and temperature control of the multipass cell were used to improve cell performance and achieve a minimum detection limit of 10 ppbv and a measurement precision of 6.4 ppbv. Finally, the potential of the developed CH4 sensor for ecological applications was verified by measuring the soil respiration of CH4 and monitoring of CH4 in the atmosphere over a long period.

Open-path anti-pollution multi-pass cell-based TDLAS sensor for the online measurement of atmospheric H2O and CO2 fluxes.

We report an open-path and anti-pollution multi-pass cell based tunable diode laser absorption spectroscopy (TDLAS) sensor, which was designed for online measurement of atmospheric H2O and CO2 fluxes. It is mainly composed of two plano-convex mirrors coated on a convex surface, which makes it different from traditional multi-pass cells. This design does not allow a direct contact between the coating layer of the lens and air, thereby realizing the anti-pollution effect of the coating layer. Two DFB lasers operating at 1392 nm and 2004 nm were employed to target H2O and CO2 absorption lines, respectively. Allan analysis of variance indicated that detection limits of H2O and CO2 were 5.98 ppm and 0.68 ppm, respectively, at an average time of 0.1 s. The sensor performance was demonstrated by measuring CO2 and H2O flux emissions at Jiangdu Agricultural Monitoring Station in Jiangsu Province. The results were compared with those obtained using the commercial instrument LI-7500, which is based on non-dispersive infrared technology. The developed gas analysis instrument exhibited good consistency with commercial instruments, and its accuracy was comparable; thus, it has strong application prospects for flux measurements in any ecosystem.

Simultaneous Sensitive Determination of δ13C, δ18O, and δ17O in Human Breath CO2 Based on ICL Direct Absorption Spectroscopy.

Previous research revealed that isotopes 13C and 18O of exhaled CO2 have the potential link with Helicobacter pylori; however, the 17O isotope has received very little attention. We developed a sensitive spectroscopic sensor for simultaneous δ13C, δ18O, and δ17O analysis of human breath CO2 based on mid-infrared laser direct absorption spectroscopy with an interband cascade laser (ICL) at 4.33 µm. There was a gas cell with a small volume of less than 5 mL, and the pressure in the gas cell was precisely controlled with a standard deviation of 0.0035 Torr. Moreover, real-time breath sampling and batch operation were achieved in gas inlets. The theoretical drifts for δ13C, δ18O, and δ17O measurement caused by temperature were minimized to 0.017‱, 0.024‱, and 0.021‱, respectively, thanks to the precise temperature control with a standard deviation of 0.0013 °C. After absolute temperature correction, the error between the system responded δ-value and the reference is less than 0.3‱. According to Allan variance analysis, the system precisions for δ13C, δ18O, and δ17O were 0.12‱, 0.18‱, and 0.47‱, respectively, at 1 s integration time, which were close to the real-time measurement errors of six repeated exhalations.

A Dual-Laser Sensor Based on Off-Axis Integrated Cavity Output Spectroscopy and Time-Division Multiplexing Method.

In this article, a compact dual-laser sensor based on an off-axis integrated-cavity output spectroscopy and time-division multiplexing method is reported. A complete dual-channel optical structure is developed and integrated on an optical cavity, which allows two distributed feedback (DFB) lasers operating at wavelengths of 1603 nm and 1651 nm to measure the concentration of CO2 and CH4, simultaneously. Performances of the dual-laser sensor are experimentally evaluated by using standard air (with a mixture of CO2 and CH4). The limit of detection (LoD) is 0.271 ppm and 1.743 ppb at a 20 s for CO2 and CH4, respectively, and the noise equivalent absorption sensitivities are 2.68 × 10-10 cm-1 Hz-1/2 and 3.88 × 10-10 cm-1 Hz-1/2, respectively. Together with a commercial instrument, the dual-laser sensor is used to measure CO2 and CH4 concentration over 120 h and verify the regular operation of the sensor for the detection of ambient air. Furthermore, a first-order exponential moving average algorithm is implemented as an effective digital filtering method to estimate the gas concentration.

Laser frequency locking and intensity normalization in wavelength modulation spectroscopy for sensitive gas sensing.

A novel method for laser frequency locking and intensity normalization in wavelength modulation spectroscopy (WMS)-based gas sensor system is reported. The center spacing between two second harmonic peaks demodulated from the rising and falling edges of a scanning triangular wave (for wavelength scan) is employed as a frequency locking reference. Amplitude of the directly acquired sine signal (for wavelength modulation) in the spectral region far away from the absorption feature is employed as an intensity normalization reference. A 50 ppm CH4:N2 sample sealed in a multi-pass cell at 1 atm was employed as the target analyte for demonstration. The frequency locking significantly improves measurement accuracy, and the introduced intensity normalization method realized a ~3 times SNR improvement as compared to the commonly used 1f normalization method under frequency locking conditions. A minimum measurement precision of ~2.5 ppbv was achieved with a normalized noise equivalent absorption coefficient of 1.8 × 10-9 cm-1Hz-1/2.

Dual-Gas Sensor of CH4/C2H6 Based on Wavelength Modulation Spectroscopy Coupled to a Home-Made Compact Dense-Pattern Multipass Cell.

A sensitive dual-gas sensor for the detection of CH4 and C2H6 is demonstrated. Two tunable semiconductor lasers operating at 1.653 µm (for CH4 monitoring) and 1.684 µm (for C2H6) were used as the light source for spectroscopic measurements of CH4 and C2H6. Long-path absorption in a home-made compact dense-pattern multipass cell (Leff = 29.37 m) was employed, combined with wavelength modulation and second harmonic detection. Simultaneous detection of CH4 and C2H6 was achieved by separated wavelength modulations of the two lasers. Modulation frequencies and amplitudes were optimized for sensitivity detection of CH4 and C2H6 simultaneously. The dual-gas sensor exhibits 1σ detection limits of 1.5 ppbv for CH4 in 140 s averaging time and 100 ppbv for C2H6 in 200 s.