19 research outputs found

    Thermoacoustically driven flame motion and heat release variation in a swirl-stabilized gas turbine burner investigated by LIF and chemiluminescence

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    Laser-induced fluorescence and chemiluminescence, both phase-locked to the dominant acoustic oscillation, are used to investigate phenomena related to thermoacoustic instability in a swirl-stabilized industrial scale gas turbine burner. The observed sinusoidal phase-averaged flame motion in axial (main flow) direction is analyzed using different schemes for defining the flame position. Qualitative agreement between experimental data and theoretical analysis of the observed flame motion is obtained, interpreted as originating primarily from variation of the burning velocity. The heat release variation during an acoustic cycle is determined from the sinusoidally varying total OH* chemiluminescence intensit

    Identification of H2_2CCC as a diffuse interstellar band carrier

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    We present strong evidence that the broad, diffuse interstellar bands (DIBs) at 4881 and 5450\,\AA are caused by the B\,^1B1_1\,\leftarrow\,X\,^1A1_1 transition of H2_2CCC (l-C3_3H2_2). The large widths of the bands are due to the short lifetime of the B\,^1B1_1 electronic state. The bands are predicted from absorption measurements in a neon matrix and observed by cavity ring-down in the gas phase and show exact matches to the profiles and wavelengths of the two broad DIBs. The strength of the 5450\,\AA DIB leads to a l-C3_3H2_2 column density of 5×1014\sim5\times10^{14} cm2^{-2} towards HD\,183143 and 2×1014\sim2\times10^{14}\,cm2^{-2} to HD\,206267. Despite similar values of EE(BVB-V), the 4881 and 5450\,\AA DIBs in HD\,204827 are less than one third their strength in HD\,183143, while the column density of interstellar C3_3 is unusually high for HD\,204827 but undetectable for HD\,183143. This can be understood if C3_3 has been depleted by hydrogenation to species such as l-C3_3H2_2 towards HD\,183143. There are also three rotationally resolved sets of triplets of l-C3_3H2_2 in the 6150-6330\,\AA region. Simulations, based on the derived spectroscopic constants and convolved with the expected instrumental and interstellar line broadening, show credible coincidences with sharp, weak DIBs for the two observable sets of triplets. The region of the third set is too obscured by the α\alpha-band of telluric O2_2.Comment: 22 pages, 9 figure

    Distributions d'énergie cinétique de la dissociation d'ions du Fluoroéthène et du 1,1-difluoroéthène.

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    The unimolecular dissociation of energy-selected fluoroethene and 1,1-difluoroethene ions has been investigated by threshold photoelectron photoion coincidence TPEPICO) technique. The breakdown diagrams of the 1,1-difluorethene and fluoroethene have been recorded between 13-22 eV. From time-of-flight (TOF) spectra, complete distributions of the kinetic energy released (KERD) in the dissociation of these energy-selected ions have been derived. For the HF-loss reaction channel, the KERD peaks at about 200 meV for low excitation energies but becomes thermal at higher excitation energies. For the F-loss channel, the KERD peaks at zero kinetic energy for low excitation energies but at about 200 meV for high excitation energy. The analysis of the KERD provides evidence that consecutive fragmentation takes place for the 1,1-difluoroethene at energies above 19 eV

    Réactions statistiques et non-statistiques dans les ions Fluorométhane sélectionnés en énergie.

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    The unimolécular reactions of the fluoromethane ion have been investigated by the threshold photoelectron photoion coincidence technique (TPIPECO). The breakdown curves have been measured in the energy range between the adiabatic ionization potential of 12.53 eV and 21 eV. In this enery range the formation of the CH2F+, CHF+, CH2+, CH3+, and CF+ fragment ions is observed. The appearance energies (AE) for these ions at 300K are 13.2, 13.91, 13.93, 14.51 and <17.7 eV respectively. The 0K threshold energy for the formation of CH2F+ ions is 13.37 eV. Two different pathways for the unimolecular reaction of the fluoromethane ion can be distinguished.The reaction proceeding through the electronic ground state of the ion is entirely statistical. In contrast to this the reaction occurring through the first electronic excited state shows non-statistical behaviour. The two pathways are distinguished via the kinetic energy released in the respective dissociation channels. While all thermodynamically allowed reaction channels are observed on the ion ground state potential, the first excited state seems to decay predominantly by F loss reaction

    Gas-Phase Electronic Spectrum of the Tropyl C 7

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    Les réactions élémentaires des ions 1,1-Difluoroéthène sélectionnés en énergie.

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    The dissociative photoionization dynamics of 1,1-difluoroethene has been investigated by TPEPICO using synchrotron radiation. The breakdown diagram has been build. The attention has been focussed on C2HF+ (HF-loss) channel

    Réaction chimique dans l'agrégat ionisé constitué de 1,1-Difluoroéthène et d'Argon.

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    The preparation conditions of 1,1-difluoroethene-Ar clusters has been investigated by photoionization using synchrotron radiation. The nature of the products has been identified by a quadrupole mass spectrometer
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