Lock-in Amplifier Time Constant Research Articles

Development of a 443 nm diode laser-based differential photoacoustic spectrometer for simultaneous measurements of aerosol absorption and NO2

Measurement of ambient aerosol and nitrogen dioxide (NO2) is important as they are major pollutants from the burning of fossil fuel and biomass. In the present work, a differential photoacoustic spectrometer (D-PAS) was developed for simultaneous, online measurements of aerosol optical absorption and NO2 concentration. A novel photoacoustic resonator was designed and employed in the D-PAS for controlling a large flow rate, improving response time, and keeping the flow noise at a low level. The detection limits of 1.0 Mm−1 and 0.87 ppb for aerosol absorption and NO2 concentration measurements were achieved with a lock-in amplifier time constant of 1 s. The D-PAS accuracy was demonstrated by performing a long-time, continuous measurement of aerosol, and NO2 in ambient air. The measured results of NO2 are consistent with the NOx analyzer and environmental monitoring station results.

Photoacoustic detection of acetone in N2 and synthetic air using a high power UV LED

The performance of a photoacoustic trace gas sensor for the detection of acetone in N2 and synthetic air is reported. The sensor system utilises an amplitude modulated UV LED. The light source has an emission maximum at 278 nm and a maximum CW output power of 300 mW according to the datasheet. Three different collimating and focusing approaches have been investigated to guide the highly divergent LED light into the acoustic resonator of the photoacoustic measurement cell. A 3D printed aluminium cell was designed to optimize light coupling by simultaneously minimizing the photoacoustic background signal generation. Hence, the diameter of the resonator was set to a comparable large diameter of 10 mm and the inner walls of the resonator were mirror polished. The additive manufacturing procedure allowed for integration of a spirally formed gas channel, enabling gas heating prior to detection. The sensor performance was investigated by measuring acetone in N2 and synthetic air at different concentrations. The UV LED current was set to 86 % of the maximum value according to the datasheet of the light source in order to increase the lifetime and thermal stability. An Allan-Werle deviation analysis validates a stable sensor performance. The limit of detection (LoD) was determined at a 3σ noise level with a 10 s lock-in amplifier time constant by sampling data points over 20 s with a data acquisition rate of 5 Hz. LoDs of 80.8 ppbV and 19.6 ppbV were obtained for acetone in N2 and synthetic air, respectively.

A 3D-Printed Microresonator Based on the Quartz-Enhanced Photoacoustic Spectroscopy Sensor for Methane Detection

A 3D-printed microresonator based on a quartz tuning fork has been developed. The sensor performance is evaluated by detection of methane with a fiber-coupled distributed feedback diode laser. In combination with wavelength modulation spectroscopy, a minimum detectable concentration of 15.6 ppb by volume is achieved at atmospheric pressure with an 8-mW average optical excitation power and a lock-in amplifier time constant of 1 s, which corresponds to a 1σ normalized noise equivalent absorption coefficient of 5·10–9 cm–1·W/Hz1/2. An Allan variance analysis shows that the system has long-term stability and can serve as the basis for a portable gas analyzer. Approaches to improve the current sensor performance are also discussed. This design greatly reduces the time of manufacturing the microresonator.

Compact quantum cascade laser based quartz-enhanced photoacoustic spectroscopy sensor system for detection of carbon disulfide.

A compact gas sensor system based on quartz-enhanced photoacoustic spectroscopy (QEPAS) employing a continuous wave (CW) distributed feedback quantum cascade laser (DFB-QCL) operating at 4.59 µm was developed for detection of carbon disulfide (CS2) in air at trace concentration. The influence of water vapor on monitored QEPAS signal was investigated to enable compensation of this dependence by independent moisture sensing. A 1 σ limit of detection of 28 parts per billion by volume (ppbv) for a 1 s lock-in amplifier time constant was obtained for the CS2 line centered at 2178.69 cm-1 when the gas sample was moisturized with 2.3 vol% H2O. The work reports the suitability of the system for monitoring CS2 with high selectivity and sensitivity, as well as low sample gas volume requirements and fast sensor response for applications such as workplace air and process monitoring at industry.

CW DFB RT diode laser-based sensor for trace-gas detection of ethane using a novel compact multipass gas absorption cell

The development of a continuous wave, thermoelectrically cooled (TEC), distributed feedback diode laser-based spectroscopic trace-gas sensor for ultra-sensitive and selective ethane (C2H6) concentration measurements is reported. The sensor platform used tunable diode laser absorption spectroscopy (TDLAS) and wavelength modulation spectroscopy as the detection technique. TDLAS was performed using an ultra-compact 57.6 m effective optical path length innovative spherical multipass cell capable of 459 passes between two mirrors separated by 12.5 cm and optimized for the 2.5–4 μm range TEC mercury–cadmium–telluride detector. For an interference-free C2H6 absorption line located at 2,976.8 cm−1, a 1σ minimum detection limit of 740 pptv with a 1 s lock-in amplifier time constant was achieved.

Ultra-sensitive carbon monoxide detection by using EC-QCL based quartz-enhanced photoacoustic spectroscopy

A quartz-enhanced photoacoustic spectroscopy (QEPAS) based sensor for carbon monoxide detection at ppbv levels was developed with a 4.65 μm external-cavity quantum cascade laser operating both in continuous wave (cw) and pulsed modes. A 23-fold enhancement of the measured CO signal amplitude was obtained when water vapor, acting as a catalyst for vibrational energy transfer, was added to the targeted analyte mixture. In the cw mode, a noise-equivalent sensitivity (NES, 1σ) of 2 ppbv was achieved at a gas pressure of 100 Torr, for 1-s lock-in amplifier (LIA) time constant (TC), which corresponds to a normalized noise equivalent absorption coefficient (NNEA) of $1.48\times 10^{-8}~\mathrm{cm}^{-1}\,\mathrm{W}/\sqrt{\mathrm{Hz}}$ . In the pulsed mode, the determined NES and NNEA were 46 ppbv and $1.07\times 10^{-8}~\mathrm{cm}^{-1}\,\mathrm{W}/\sqrt{\mathrm{Hz}}$ , respectively, for a 3-ms LIA TC at atmospheric pressure with a laser scan rate of 18 cm-1/s and a 50 % duty cycle. An intercomparison between cw and pulsed QEPAS-based CO detection is also reported.

Continuous wave, distributed feedback diode laser based sensor for trace-gas detection of ethane

The development of a continuous wave (CW), thermoelectrically cooled (TEC), distributed feedback (DFB) laser diode based spectroscopic trace-gas sensor for ultra-sensitive and selective ethane (C2H6) concentration measurements is reported. The sensor platform used tunable diode laser absorption spectroscopy (TDLAS) based on a 2f wavelength modulation (WM) detection technique. TDLAS was performed with a 100 m optical path length astigmatic Herriott cell. For an interference free C2H6 absorption line located at 2976.8 cm−1 a 1σ minimum detection limit of 240 pptv (part per trillion by volume) with a 1 second lock-in amplifier time constant was achieved. In addition, reliable and long-term sensor performance was obtained when operating the sensor in an absorption line locked mode.

Phase-shift off-axis cavity-enhanced absorption detector of nitrogen dioxide

Phase-sensitive, off-axis cavity-enhanced absorption spectroscopy techniques with a rectangular pulse current modulated violet diode laser (∼404 nm) were applied to measurement of nitrogen dioxide (NO2) in diluted standard mixture and laboratory air. An optical cell of an NO2 detector was bounded by two plano-concave mirrors with a diameter of 7.75 mm and a reflectivity of 0.999, separated by a distance of 43 cm. The phase shift measurements due to Rayleigh scattering extinction were used for calibration of the detector. NO2 sensitivities were extracted from synchronous measurements of either the cavity output light intensity or the phase shift induced by the cavity. NO2 noise equivalent detection limit (S/N = 1) of 1–2 ppbv was demonstrated for the intensity measurements with a lock-in amplifier time constant of 1 s. From the Allan plot of the intensity measurements the NO2 minimum concentration was estimated to be 0.24 ppbv in 80 s at atmospheric pressure.

Ammonia detection by use of quartz-enhanced photoacoustic spectroscopy with a near-IR telecommunication diode laser

A gas sensor based on quartz-enhanced photoacoustic detection and a fiber-coupled telecommunication distributed-feedback diode laser was designed and characterized for trace NH3 monitoring at a 1.53-microm wavelength (overtone absorption region). Signal and noise dependence on gas pressure were studied to optimize sensor performance. The ammonia concentration resulting in a noise-equivalent signal was found to be 0.65 parts per million by volume with 38-mW optical excitation power and a lock-in amplifier time constant of 1 s. This corresponds to a normalized absorption sensitivity of 7.2 x 10(-9) cm(-1) W/Hz1/2, comparable with detection sensitivity achieved in conventional photoacoustic spectroscopy. The sensor architecture can be the basis for a portable gas analyzer.

Off-axis continuous-wave cavity-enhanced absorption spectroscopy of narrow-band and broadband absorbers using red diode lasers

We present an application of continuous-wave (cw) cavity-enhanced absorption spectroscopy (CEAS) with off-axis alignment geometry of the cavity and with time integration of the cavity output intensity for detection of narrow-band and broadband absorbers using single-mode red diode lasers at λ=687.1 nm and λ=662 nm, respectively. Off-axis cw CEAS was applied to kinetic studies of the nitrate radical using a broadband absorption line at λ=662 nm. A rate constant for the reaction between the nitrate radical and E-but-2-eneof (3.78±0.17)×10-13 cm3 molecule-1 s-1 was measured using a discharge-flow system. A nitrate-radical noise-equivalent (1σ≡ root-mean-square variation of the signal) detection sensitivity of 5.5×109 molecule cm-3 was achieved in a flow tube with a diameter of 4 cm and for a mirror reflectivity of ∼99.9% and a lock-in amplifier time constant of 3 s. In this case, a noise-equivalent fractional absorption per one optical pass of 1.6×10-6 was demonstrated at a detection bandwidth of 1 Hz. A wavelength-modulation technique (modulation frequency of 10 kHz) in conjunction with off-axis cw CEAS has also been used for recording 1f- and 2f-harmonic spectra of the RR(15) absorption of the b1Σg+-X3Σg- (1,0) band of molecular oxygen at \(\overline{\nu}\)=14553.947 cm-1. Noise-equivalent fractional absorptions per one optical pass of 1.35×10-5, 6.9×10-7 and 1.9×10-6 were obtained for direct detection of the time-integrated cavity output intensity, 1f- and 2f-harmonic detection, respectively, with a mirror reflectivity of ∼99.8%, a cavity length of 0.22 m and a detection bandwidth of 1 Hz.

Oxygen sensing using single frequency GaAs-AlGaAs DFB laser diodes and VCSELs

Oxygen detection using a GaAs-AlGaAs distributed feedback laser diode emitting at a wavelength of 761 nm is demonstrated for the first time. Using wavelength modulation spectroscopy with harmonic detection the authors have achieved a detection limit of 20 ppm.m with a lock-in amplifier time constant of 33.3 ms. The first results comparing the relative merits of VCSELs and DFB laser diodes for sensing applications are also shown.

Hot Wire Measurement of Velocity Gradients in a Fluid Flow

Theme paper presents the results of an experimental investigation of a technique to directly measure the first and second spatial velocity derivatives in a fluid flow. The technique's utility lies in the fact that it does not depend on graphical differentiation or computer curve fitting methods as do the usual techniques for obtaining spatial velocity derivatives. The techniques utilizes an oscillating hot wire anemometer probe traversing the flow in a direction perpendicular to the mean flow. The response signal is processed first through an electronic linearizer and then through a lockin amplifier. The spatial derivatives are contained in the coefficients of the first and second harmonics of the wire response signal from the lock-in amplifier which is tuned to the frequency of the oscillating probe. The investigation compares the experimental results with graphical and computer derived profiles with a favorable result. A check is also performed to confirm the range of independence of the results from changes in the parameters r, co, and R; the lock-in amplifier time constant, the frequency of oscillation, and the amplitude of oscillation.