Sensing of formaldehyde using a distributed feedback interband cascade laser emitting around 3493 nm.

We have demonstrated sensing of formaldehyde (H(2)CO) using a room-temperature distributed feedback interband cascade laser (ICL) emitting around 3493 nm. The ICL has been characterized and proved to be very suitable for tunable laser spectroscopy (TLS). The H(2)CO TLS spectra were recorded in direct absorption mode and showed excellent agreement with the Pacific Northwest National Laboratory database. The measurements reported here were taken from a series of measurements of a mixture of H(2)CO in air obtained by vaporizing a solution also containing methanol and formic acid. We obtained a resolution limit better than 1 ppm × m assuming a relative absorption of 10(-3).

Methodology for detection of carbon monoxide in hot, humid media by telecommunication distributed feedback laser-based tunable diode laser absorption spectrometry.

Detection of carbon monoxide (CO) in combustion gases by tunable diode laser spectrometry is often hampered by spectral interferences from H2O and CO2. A methodology for assessment of CO in hot, humid media using telecommunication distributed feedback lasers is presented. By addressing the R14 line at 6395.4 cm(-1), and by using a dual-species-fitting technique that incorporates the fitting of both a previously measured water background reference spectrum and a 2f-wavelength modulation lineshape function, percent-level concentrations of CO can be detected in media with tens of percent of water (c(H2O)≤40%) at T≤1000 °C with an accuracy of a few percent by the use of a single reference water spectrum for background correction.

Interband Cascade Laser Arrays for Simultaneous and Selective Analysis of C1-C5 Hydrocarbons in Petrochemical Industry.

The detection and measurement of hydrocarbons are of high interest for a variety of applications, for example within the oil and gas industry from extraction throughout the complete refining process, as well as for environmental monitoring and for portable safety devices. This paper presents a highly sensitive, selective, and robust tunable laser analyzer that has the capability to analyze several components in a gas sample stream. More specifically, a multi-gas system for simultaneous detection of C1 to iC5 hydrocarbons, using a room temperature distributed feedback interband cascade laser array, emitting in the 3.3 µm band has been realized. It combines all the advantages of the tunable laser spectroscopy method for a fast, sensitive, and selective in-line multicomponent tunable laser analyzer. Capable of continuous and milliseconds fast monitoring of C1-iC5 hydrocarbon compositions in a process stream, the analyzer requires no consumables (e.g., purging, carrier gas) and no in-field calibration, enabling a low cost of ownership for the analyzer. The system was built based on an industrial GasEye series platform and deployed for the first time in field at Preem refinery in Lysekil, Sweden, in autumn 2018. Results of the measurement campaign and comparison with gas chromatography instrumentation are presented.

Faraday modulation spectrometry of nitric oxide addressing its electronic X2Π - A2Σ+ band: II. Experiment.

A first demonstration of Faraday modulation spectrometry (FAMOS) of nitric oxide (NO) addressing its strong electronic X(2)Π(ν″ = 0) - A(2)Σ(+)(ν(') = 0) band is presented. The instrumentation was constructed around a fully diode-laser-based laser system producing mW powers of ultraviolet light targeting the overlapping Q(22)(21/2) and R(12)Q(21/2) transitions at ∼226.6 nm. The work verifies a new two-transition model of FAMOS addressing the electronic transitions in NO given in an accompanying work. Although the experimental instrumentation could address neither the parameter space of the theory nor the optimum conditions, the line shapes and the pressure dependence could be verified under low-field conditions. NO could be detected down to a partial pressure of 13 µTorr, roughly corresponding to 10 ppb·m for an atmospheric pressure sample, which demonstrates the feasibility of FAMOS for sensitive detection of NO addressing its strong electronic band.

Faraday modulation spectrometry of nitric oxide addressing its electronic X2Π - A2Σ+ band: I. Theory.

We give a simple two-transition model of Faraday modulation spectrometry (FAMOS) addressing the electronic X(2)Π(ν('') = 0) - A(2)Σ(+)(ν(') = 0) band in nitric oxide. The model is given in terms of the integrated line strength, S, and first Fourier coefficients for the magnetic-field-modulated dispersive line shape function. Although the two states addressed respond differently to the magnetic field (they adhere to the dissimilar Hund coupling cases), it is shown that the technique shares some properties with FAMOS when rotational-vibrational Q-transitions are targeted: the line shapes have a similar form and the signal strength has an analogous magnetic field and pressure dependence. The differences are that the maximum signal appears for larger magnetic field amplitudes and pressures, ∼1500 G and ∼200 Torr, respectively.

Tunable-diode-laser spectroscopy of C(2)H(2) using a 3.03 microm GaInAsSb/AlGaInAsSb distributed-feedback laser.

The mid-IR region beyond 3 microm is very attractive for gas sensing, since the fundamental absorption bands of several hydrocarbons are located in this range. We demonstrated, for the first time to our knowledge, the use of a novel GaInAsSb/AlGaInAsSb distributed-feedback laser emitting around 3.03 microm in a tunable-diode laser-spectroscopy application. The laser operates in continuous mode at room temperature with excellent single-mode and tuning properties. A comparison of the measurement results was made with the recently updated data on C212H(2) found in the HITRAN 2008 compilation. A good agreement was found between the measurements and the database. Wavelength modulation spectroscopy of acetylene at ambient conditions was made, and a sensitivity of 18 ppb (parts per billion) per meter at an integration time of 3 s corresponding to a relative absorption of 5 x 10(-6) was obtained. The optimum detection limit of the acetylene measurement in this wavelength modulation spectroscopy setup was better than 1.5 ppb m at an integration time of 600 seconds.