Custom-built light-pipe cell for high-resolution infrared absorption spectroscopy of tritiated water vapor and other hazardous gases.

We present a new custom-built cell for high-resolution absorption spectroscopy of hazardous gases. The use of an aluminum light-pipe enables sensitive detection due to the small tube diameter and an increased particle density in the interaction volume for a limited analyte amount in the cell, while avoiding additional surfaces such as mirrors. To demonstrate this, we have used the cell to measure tritiated water isotopologues (HTO and traces of T2O) for which spectroscopic data is scarce, due to the challenge of performing spectroscopy of these highly radio-chemical aggressive substances. For this purpose, the new cell also features the efficient inline-production of tritiated water. In this paper we present the concept of the light-pipe cell and demonstrate its performance with a high-resolution absorption spectrum of gaseous HTO generated inside of this cell.

Laser-induced plasmas in ambient air for incoherent broadband cavity-enhanced absorption spectroscopy.

The emission from a laser-induced plasma in ambient air, generated by a high power femtosecond laser, was utilized as pulsed incoherent broadband light source in the center of a quasi-confocal high finesse cavity. The time dependent spectra of the light leaking from the cavity was compared with those of the laser-induced plasma emission without the cavity. It was found that the light emission was sustained by the cavity despite the initially large optical losses of the laser-induced plasma in the cavity. The light sustained by the cavity was used to measure part of the S(1) ← S(0) absorption spectrum of gaseous azulene at its vapour pressure at room temperature in ambient air as well as the strongly forbidden γ-band in molecular oxygen: b(1)Σ(g)(+)(ν'=2)←X(3)Σ(g)(-)(ν''=0).

Incoherent broad-band cavity-enhanced absorption spectroscopy of the marine boundary layer species I2, IO and OIO.

The novel combination of incoherent broad-band cavity-enhanced absorption spectroscopy (IBBCEAS) and a discharge-flow tube for the study of three key atmospheric trace species, I(2), IO and OIO, is reported. Absorption measurements of I(2) and OIO at lambda=525-555 nm and IO at lambda=420-460 nm were made using a compact cavity-enhanced spectrometer employing a 150 W short-arc Xenon lamp. The use of a flow system allowed the monitoring of the chemically short-lived radical species IO and OIO to be conducted over timescales of several seconds. We report detection limits of approximately 26 pmol mol(-1) for I(2) (L=81 cm, acquisition time 60 s), approximately 45 pmol mol(-1) for OIO (L=42.5 cm, acquisition time 5 s) and approximately 210 pmol mol(-1) for IO (L=70 cm, acquisition time 60 s), demonstrating the usefulness of this approach for monitoring these important species in both laboratory studies and field campaigns.

Incoherent broadband cavity-enhanced absorption spectroscopy in the near-ultraviolet: application to HONO and NO2.

The first application of incoherent broadband cavity-enhanced absorption spectroscopy (IBBCEAS) in the near-ultraviolet for the simultaneous detection of two key atmospheric trace species, HONO and NO2, is reported. For both compounds the absorption is measured between 360 and 380 nm with a compact cavity-enhanced spectrometer employing a high power light-emitting diode. Detection limits of approximately 4 ppbv for HONO and approximately 14 ppbv for NO2 are reported for a static gas cell setup using a 20 s acquisition time. Based on an acquisition time of 10 min and an optical cavity length of 4.5 m detection limits of approximately 0.13 ppbv and approximately 0.38 ppbv were found for HONO and NO2 in a 4 m3 atmospheric simulation chamber, demonstrating the usefulness of this approach for in situ monitoring of these important species in laboratory studies or field campaigns.

High-resolution Fourier-transform cavity-enhanced absorption spectroscopy in the near-infrared using an incoherent broad-band light source.

An incoherent broad-band cavity-enhanced absorption (IBB-CEA) set-up was used in combination with a Fourier-transform (FT) spectrometer in order to explore the potential of this technique for high-resolution molecular spectroscopy in the near-infrared region. Absorption spectra of overtone bands of CO2, OCS, and HD18O were measured between 5800 and 7000 cm(-1) using a small sampling volume (1100 cm3, based on a 90 cm cavity length). The quality of the spectra in this study is comparable to that obtained with Fourier transform spectrometers employing standard multi-pass reflection cells, which require substantially larger sampling volumes. High-resolution methods such as FT-IBB-CEAS also provide an elegant way to determine effective mirror reflectivities (R(eff), i.e. a measure of the inherent overall cavity loss) by using a calibration gas with well-known line strengths. For narrow absorption features and non-congested spectra this approach does not even require a zero-absorption measurement with the empty cavity. Absolute cross-sections or line strengths of a target species can also be determined in one single measurement, if gas mixtures with known partial pressures are used. This feature of FT-IBB-CEAS reduces systematic errors significantly; it is illustrated based on CO2 as calibration gas.

Fourier-transform cavity-enhanced absorption spectroscopy using an incoherent broadband light source.

A cavity-enhanced absorption setup employing an incoherent broadband light source was used in combination with a Fourier-transform spectrometer to measure the spin-forbidden B-band of gaseous oxygen at approximately 688 nm and several weak absorption transitions of water vapor in the same spectral region at room temperature in ambient air. The experiments demonstrate that the sensitivity of a Fourier-transform spectrometer can be significantly improved by increasing the effective path length, while retaining a rather small sample volume. In comparison with a single-pass absorption measurement, we report a path-length enhancement factor of 200 and an improvement of the signal-to-noise ratio of approximately 6 in the present cavity-enhanced absorption experiment. The practical advantages and limitations of this novel approach are outlined and potential applications are briefly discussed.

High sensitivity in situ monitoring of NO3 in an atmospheric simulation chamber using incoherent broadband cavity-enhanced absorption spectroscopy.

We describe the application of incoherent broadband cavity-enhanced absorption spectroscopy (IBBCEAS) for the in situ detection of atmospheric trace gases and radicals (NO3, NO2, O3, H2O) in an atmospheric simulation chamber under realistic atmospheric conditions. The length of the optical cavity across the reaction chamber is 4.5 m, which is significantly longer than in previous studies that use high finesse optical cavities to achieve high absorption sensitivity. Using a straightforward spectrometer configuration, we show that detection limits corresponding to typical atmospheric concentrations can be achieved with a measurement time of seconds to a few minutes. In particular, with only moderate reflectivity mirrors, we report a measured sensitivity of 4 pptv to NO3 in a 1 min acquisition time. The high spatial and temporal resolution of the IBBCEAS method and its pptv sensitivity to NO3 makes it useful in laboratory studies of atmospheric processes as well as having obvious potential for field measurements.

The visible absorption spectrum of OBrO, investigated by Fourier transform spectroscopy.

By the utilization of a new laboratory method to synthesize OBrO employing an electric discharge, the visible absorption spectrum of gaseous OBrO has been investigated. Absorption spectra of OBrO have been recorded at 298 K, using a continuous-scan Fourier transform spectrometer at a spectral resolution of 0.8 cm(-1). A detailed vibrational and rotational analysis of the observed transitions has been carried out. The FTS measurements provide experimental evidence that the visible absorption spectrum of OBrO results from the electronic transition C(2A2)-X(2B1). Vibrational constants have been determined for the C(2A2) state (omega(1) = 648.3 +/- 1.9 cm(-1) and omega 2 = 212.8 +/- 1.2 cm(-1)) and for the X(2B1) state (omega 1 = 804.1 +/- 0.8 cm(-1) and omega 2 = 312.2 +/- 0.5 cm(-1)). The vibrational bands (1,0,0), (2,0,0), and (1,1,0) show rotational structure, whereas the other observed bands are unstructured because of strong predissociation. Rotational constants have been determined experimentally for the upper electronic state C(2A2). By modeling the band contours, predissociation lifetimes have been estimated. Further, an estimate for the absorption cross-section of OBrO has been made by assessing the bromine budget within the gas mixture, and atmospheric lifetimes of OBrO have been calculated using a photochemical model.

Principal and independent components analysis of overlapping spectra in the context of multichannel time-resolved absorption spectroscopy.

The separation of overlapping absorption spectra in the context of multichannel time-resolved absorption spectroscopy and chemical kinetics is a particular case in the general problem of splitting the observed data into several linear components. Here, principal and independent components analysis are applied to kinetic data of iodine--ozone chemistry, which contains overlapping spectra of different absorbers. The objective of this work is to demonstrate a method which in spite of this overlap is able to extract separated time traces of such absorbers. These time traces are clearly a pre-requisite for any further accurate quantitative analysis. The statistical properties of data recordings obtained from flash photolysis of I(2) and O(3) have been studied to check if the requirements of the model are fulfilled. Results of separation in appropriate spectral windows displaying overlapped vibrational features are presented. Validation is made using prior information and conventional techniques.