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The development of interband cascade lasers (ICLs) has made the strong C-H transitions in the 3 μm spectral region increasingly accessible. We present the demonstration of a single mode distributed feedback ICL coupled to a V-shaped optical cavity in an optical feedback cavity-enhanced absorption spectroscopy (OF-CEAS) experiment. We achieved a minimum detectable absorption coefficient, αmin, of (7.1±0.2)×10-8 cm-1 for a spectrum of CH4 at 3.24 μm with a two second acquisition time (100 scans averaged). This corresponds to a detection limit of 3 ppb CH4 at atmospheric pressure, which is comparable to previously reported OF-CEAS instruments with diode lasers or quantum cascade lasers. The ability to frequency lock an ICL source in the important 3 μm region to an optical cavity holds great promise for future spectroscopic applications. [ABSTRACT FROM AUTHOR]

The formation of carbon nanoparticles in low pressure magnetized H2/CH4 and H2/C2H2 plasmas is investigated using infrared quantum cascade laser absorption, mass spectrometry, and electrostatic probe measurements. Results showed that dust formation is correlated to the presence of a significant amount of large positively charged hydrocarbon ions. Large negative ions or neutral hydrocarbon were not observed. These results, along with a qualitative comparison of diffusion and reaction characteristic, suggest that a positive ion may contribute to the growth of nanoparticles in hydrocarbon magnetized plasmas. [ABSTRACT FROM PUBLISHER]

A compact and transportable three channel quantum cascade laser system (TRIPLE Q) based on mid-infrared absorption spectroscopy has been developed for time-resolved plasma diagnostics. The TRIPLE Q spectrometer encompasses three independently controlled quantum cascade lasers (QCLs), which can be used for chemical sensing, particularly for gas phase analysis of plasmas. All three QCLs are operated in the intra-pulse mode with typical pulse lengths of the order of 150 ns. Using a multiplexed detection, a time resolution shorter than 1 μs can be achieved. Hence, the spectrometer is well suited to study kinetic processes of multiple infrared active compounds in reactive plasmas. A special data processing and analysis technique has been established to account for time jitter effects of the infrared emission of the QCLs. The performance of the TRIPLE Q system has been validated in pulsed direct current plasmas containing N2O/air and NO2/air. [ABSTRACT FROM AUTHOR]

The absorption spectra of the fundamental bands of the free radicals 10B16O and 11B16O in their ground 2Σ+ states have been measured in natural abundance and at Doppler limited resolution using diode laser spectroscopy. The band origins are found to be 1915.30674(14) and 1861.92409(13) cm−1, respectively. The rotational constants for the lower states are 1.877680(22) and 1.773421(10) cm−1, which are in excellent agreement with the microwave values for B0. Assuming a linear dependence of Bv on (v+1/2) the derived value of re is 1.204552(5) A˚. [Copyright &y& Elsevier]

A compact and transportable two laser beam infrared (TOBI) system based on infrared absorption spectroscopy has been developed for time-resolved plasma diagnostics. The TOBI system contains two independent tunable diode lasers which can be directed through a plasma or into a multipass cell for exhaust gas detection. Rapid scan software with real-time line shape fitting provides a time resolution up to 10 μs to study chemical kinetic processes of infrared active compounds in plasmas. The capabilities of the TOBI system have been demonstrated in plasmas of pulsed H[sub 2]–N[sub 2] surface wave and in pulsed air–CH[sub 4] dc discharges. © 2003 American Institute of Physics. [ABSTRACT FROM AUTHOR]

The potential of an approach combining a pulsed microwave discharge with a catalytic packed bed reactor for the oxidation of volatile organic compounds (VOC) has been studied. The ignition of the plasma has been made possible by inserting ferroelectric BaTiO3 pellets inside the microwave excitator. As a test VOC molecule, acetylene (C2H2) in an amount of 200 ppm in dry air was used. The total oxidation products CO and CO2 have been monitored downstream of the plasma region by tuneable diode laser absorption spectroscopy in the infrared region. The oxidative efficiency was found to increase linearly with the pulse repetition rate. The oxidative efficiency and the CO2/CO selectivity were considerably enhanced when the catalyst was located inside the plasma region, which shows the synergetic effect of the plasma-catalyst combination. [ABSTRACT FROM AUTHOR]

In Ar and He radio-frequency (RF) plasmas with admixtures of C2H2 and CH4 the hydrocarbon chemistry has been studied in relation to dust particle formation by means of infrared tunable diode laser absorption spectroscopy (TDLAS) combined with Fourier transform infrared (FTIR) spectroscopy. The experiments were performed in a RF capacitively coupled parallel plate reactor at a frequency of f = 13.56 MHz, a pressure of p = 0.1 mbar and a flow rate of Φ = 8 sccm of Ar or He with admixtures of 0.5 sccm C2H2 or 1 sccm CH4. The power was P = 15 W. Using TDLAS, the temporal evolution of the concentrations of the methyl radical and of four stable molecules, C2H2, CH4, C2H4 and CO, was monitored in the plasma. Simultaneously, the growth process of the dust particles was analysed by FTIR spectroscopy. The degree of dissociation of the acetylene precursor was found to be nearly constant in the range of 96% under stabilized conditions for both the Ar and He plasmas. In contrast, the degree of dissociation of the methane precursor varied between 45% and 90% depending (i) on the appearance of dust particles in the reactor volume and (ii) on the Ar or He plasma conditions. The methyl radical concentration was found to be in the range of 1011 molecules cm−3. The concentrations of all hydrocarbon species were strongly correlated with the dynamic of the dust formation. Fragmentation efficiencies of acetylene (RF (C2 H2) = 3.2 × 1016 molecules J−1) and of methane (RF (CH4) = (0.16–2.5) × 1016 molecules J−1) and conversion efficiencies to the produced hydrocarbons (RC = (0.23–8.5) × 1014 molecules J−1) could be estimated in dependence on the discharge conditions in the RF plasma. [ABSTRACT FROM AUTHOR]