Negative Corona Current Pulses in SF6 – Air Mixtures

Current waveforms of first negative corona pulses have been measured in dry air + SF₆ mixtures at a pressure of 50 kPa and various overvoltages. Effects of changing cathode secondary electron emission were studied using a copper cathode coated by CuI and graphite. It is concluded that in the mixtures containing less than 10 % of SF₆ the negative corona pulse is associated with the formation of a cathode‐directed streamer in the immediate vicinity of the cathode. In the mixtures containing more than 20 % of SF₆ the streamer is quenched and, consequently, the discharge is governed by the Townsend ionisation mechanism fed by cathode photoemission processes.     

Dielectric properties of SF6 mixtures containing oxygen and other gases

Conclusion This paper has explored the influence of an oxygen addition on the dielectric strength of the SF₆ by numerically solving the Boltzmann equation with given cross section data. The linear variation of the dielectric strength with a mole fraction of oxygen was obtained. Similar calculations were performed for SF₆ + air for which only approximative estimates had existed in the literature. To check the results and for other practical reasons the method of the Boltzmann equation was applied to the SF₆ + He and SF₆ + N₂ mixtures, the dielectric strength of which had already been explored by other authors. In comparison with other mixtures currently studied the SF₆ + O₂ mixture reveals rather poor dielectric properties. In spite of the fact that the oxygen is an attaching gas, its addition to SF₆ and its mixtures spoils the dielectric strength. This numerical analysis exactly qualified this behaviour and it is in agreement with the few available experiments.     

The first Trichel pulse of negative corona discharge in N2 with a small admixture of SF6

Current growth waveforms of transient negative point-to-plane discharge in N₂ and in N₂ with 0·025-0·1% admixture of SF₆ at a pressure of 40 kPa have been measured and compared. The transient glow discharge regime in pure N₂ was found to be preceded by a peaked current signal of conspicuous similarity to the first Trichel pulse rise and its initial decay in N₂+SF₆ mixture. The results are in a basic agreement with a hypothesis on streamer mechanism for Trichel pulse and indicate occurrence of field emission during the rise of Trichel pulse current.     

Sulfur isotope enrichment in SF6 by high intensity CO2 laser radiation

Enrichment of ³⁴SF₆ following irradiation of SF₆?H₂ mixtures by the focused output of a pulsed TEA CO₂ laser has been studied as a function of the number of laser pulses, excitation wavelength, total pressure, and laser energy.     

Self-focussing of CO2 laser radiation in SF6

Self-focussing of high-power TEA CO₂ laser pulses for a number of 10 m P-band lines is reported in SF₆ molecular gas. Application of this effect to estimating the intensity-dependent refractive index of the gas is demonstrated.     

HF-laser performance of CO2-laser-ignited mixtures of SF6 :H2 and of S2F10 :H2

We have used a CO₂ laser to ignite mixtures of SF₆ :H₂ and S₂F₁₀ :H₂. We observed HF lasing from these mixtures when an optical resonator was constructed around the reaction cell. The HF-lasing performance of the two mixtures was compared as a function of mixture ratio, fluorine-donor pressure, and CO₂-laser frequency. Under comparable conditions, the HF-laser output for S₂F₁₀ :H₂ mixtures was typically 5–6 times greater than that for SF₆ :H₂ mixtures. Spectral output of the HF laser was coarsely resolved to provide data about the vibrational and rotational states of the HF molecule.     

Optically pumped 15.90 μm SF6 laser

Optically pumped vibrational transition lasing has been achieved for the first time in a nonlinear molecule. Laser radiation at 628.74 ± 0.02 cm^?1 was generated from SF₆ using CO₂ TEA laser excitation. The SF₆ pumping is shown to be via absorption of two photons.     

Measurement of nanoparticle temperature in a (CO2) N cluster beam using SF6 molecules as tiny probe thermometers

A temperature measurement technique using SF₆ molecules as tiny probe thermometers is described, and results are presented, for large (CO₂) _N van der Waals clusters (with N ≥ 10²) in a cluster beam. The SF₆ molecules captured by (CO₂) _N clusters in crossed cluster and molecular beams sublimate (evaporate) after a certain time, carrying information about the cluster velocity and internal temperature. Experiments are performed using detection of these molecules with an uncooled pyroelectric detector and infrared multiphoton excitation. The multiphoton absorption spectra of molecules sublimating from clusters are compared with the IR multiphoton absorption spectra of SF₆ in the incoming beam. As a result, the nanoparticle temperature in the (CO₂) _N cluster beam is estimated as T _cl < 150 K. Time-of-flight measurements using a pyroelectric detector and a pulsed CO₂ laser are performed to determine the velocity (kinetic energy) of SF₆ molecules sublimating from clusters, and the cluster temperature is found to be T _cl = 105 ± 15 K. The effects of various factors on the results of nanoparticle temperature measurements are analyzed. The potential use of the proposed technique for vibrational cooling of molecules to low temperatures is discussed.     

Strengths of the SF6 transitions pumped by a CO2 laser

The absolute intensities of the SF₆ transitions from the ground state to ν₃=1 that fall within ±1.5 GHz of the CO₂ P(14), P(18) and P(20) laser lines have been calculated. Good agreement has been found between these theoretical results and the available experimental values, especially for the firm assignments of R(28) A⁰₂ and P(33) A¹₂ for SF₆ absorption nearest the CO₂ P(14) and P(18) laser emissions, respectively.     

Vibrational predissociation of SF6 dimers and trimers

IR photo-dissociation spectra of SF₆ clusters have been studied. A He-seeded molecular beam has been attenuated by crossing it with a line tunable cw CO₂ laser of moderate power. — In the electron bombardment beam ionizer (E _el=100eV) small neutral clusters are found to fragment predominantly to the main monomer mass (SF ₅ ⁺ ). — Predissociation spectra have been calculated for clusters containing up to six SF₆-molecules invoking the dipole-dipole resonance force to lift the degeneracy of the molecule — excited molecule interaction. On the basis of these spectra, dimer and trimer concentrations have been determined quantitatively, for different molecular beam conditions.     

Absorption of CO2 laser pulses at different wavelengths by ground-state and vibrationally heated SF6

The absorption of CO₂ laser pulses by low pressure SF₆ gas has been investigated over a wide range of energy fluxes. For laser energy fluxes of 0.01–1 J cm^-2 the effective absorption cross section varies between 0.2 and 2 × 10^-18 cm². For each laser line an individual dependence on the energy is found and in some cases minor changes in the absorption behaviour seem to occur around 0.1 J cm^-2. SF₆ excited with an average vibrational energy content of up to 20 photons/molecule does not absorb measurable amounts of 9.4 μm laser light. The influence of various SF₆ and Ar pressures on the temporal shape of the transmitted pulses has been investigated.     

Multiphoton absorption of broad-band CO2 laser radiation by SF6

Increase of the emission bandwidth of a high-pressure CO₂ laser up to 1.5 cm^–1 increases the multiphoton absorption cross-section of SF₆. Comparison with the previously found [9] increased absorption for shorter pulses suggests that this is also a bandwidth effect. Spectral structures as narrow as 1 cm^–1 above the 10^th absorption step are invoked to explain the observations. The temperature effect, which disappears in the broad-band case, confirms this view.     

Molecular dissociation of SF6 by ultra-short CO2 laser pulses

We have measured the absolute dissociation probability of SF₆ gas irradiated by CO₂ laser pulses varying in duration from 0.5 nsec to 100 nsec. We find a threshold for dissociation of ? 1.4 J/cm², independent of pulse duration. For fixed energy density, the dissociation probability increases as the pulse duration decreases, but not nearly to the degree expected from theory. We have also determined the dissociation probability in the ν₂ + ν₆ combination band and find it to be 10³ times less than in the ν₃ band, in contradiction to some conclusions recently reported by Ambartzumian et al. The dissociation mechanism takes place without collisions, and if collisions occur, they tend to be detrimental to the dissociation rate.     

A KrF fast discharge laser in mixtures containing NF3, N2F4 or SF6

A fast discharge KrF laser system (λ = 248.5 nm) has been operated at 25 mJ/pulse, 3.0 MW peak power in high pressure He: Kr: fluoride mixtures containing low concentrations of both krypton and the fluorine donors N₂F₄, NF₃ and SF₆. Lasing action is reported for the first time in N₂F₄ and SF₆ with optimum energy output at 750 and 160 mJ/l respectively.     

IR absorption of highly vibrationally excited SF6

In a double-resonance experiment, the absorption of various CO₂ laser lines by sulfur hexafluoride was measured, before and after the SF₆ was pumped by a fixed frequency CO₂ laser to a level of 5 quanta/molecule. The absorption is substantially shifted to longer wavelengths. But the short wavelength wing of the absorption band is not completely bleached. Instead a shoulder of several cm⁻¹ width is left. This shoulder is probably important for the explanation of the infrared laser induced dissociation of SF₆.     

Intensitäten myonischer Röntgenlinien in SF6 und H2 plus SF6

Muonic X-ray spectra from S and F in SF₆ and H₂+SF₆ have been measured with a high-pressure gas target. Strong differences between the observed intensities of corresponding lines were found for the two cases. The results are compared with cascade calculations. The per-atom ratio between Coulomb capture in F and S was determined to be 0.96±0.09 and 1.04±0.24 for SF₆ and H₂+SF₆, respectively.     

Collisionless dissociation of SF6 using two resonant frequency CO2 laser fields

The collisionless dissociation of SF₆ has been studied using simultaneous irradiation by two frequencies from a CO₂ laser which are both nearly resonant with the SF_6v3 absorption band. It was found that the dissociation was enhanced, and occurred over a wider frequency range, than for single frequency dissociation. No threshold effect was observed for a weak resonant and a much higher energy field pumping slightly off-resonance. For such two frequency irradiation, the peak in the dissociation curve was found to be shifted to lower frequencies with respect to that for single frequency dissociation.     

Impulse breakdown characteristics of the plane-to-plane electrode system with a needle-shaped protrusion in SF6

This paper presents the impulse pre-breakdown and breakdown characteristics of the plane-to-plane electrode system with a needle-shaped protrusion in SF₆ gas. The breakdown voltage–time (V–t) characteristics and the breakdown voltage–gas pressure (V–p) characteristics of a highly non-uniform SF₆ gas gap under positive and negative lightning impulse voltages are investigated in the pressure range between 0.1 and 0.5 MPa. The pre-breakdown developments are examined by the corona current and light emission measurements with high time resolution. As a result, the dielectric strengths versus time-to-breakdown of SF₆ gas gap under positive lightning impulse voltages were nearly independent of the gas pressure. The first streamer corona was initiated at the tip of the needle electrode, and the streamer corona pulses developed with a stepwise propagation. The discharge paths were zigzag, and the branches of the discharge channel for positive polarity were created. On the other hand, the leader channel in the negative polarity was thicker and brighter than that in the positive polarity.     

Strong dependence of ir multiphoton absorption and dissociation yield of SF6 molecule on intensity (duration) of exciting laser pulse

The role of played by the intensity of the exciting TEA CO₂ laser pulses in the processes of ir multiphoton absorption (MPA) of SF₆ molecules cooled toT _R?40 K andT _v?160 K in a pulsed supersonic jet and the dissociation of SF₆ in a bulk atT?300 K under essentially collisionless conditions have been investigated. A strong dependence of MPA and the dissociation yield on pulse intensity were observed. The frequency dependences of the intensity effects were studied.     

Dynamics and correlated performance of a photo-triggered discharge-pumped HF laser using SF6 with hydrogen or ethane

3 , has been performed in Ne/SF₆/H₂ and Ne/SF₆/C₂H₆ mixtures. Parameters involved have been the storage line capacitance and the circuit inductance, the capacitors charging voltage, the RH-molecule type and partial pressure, and the X-ray dose for the preionization. High laser performance has been achieved with C₂H₆: an output energy up to 3 J corresponding to a specific energy of 9.6 J/l at an efficiency of 4.7%, which strengthens the advantage of the photo-triggering technique to energize high-power HF lasers. However the optimum performance achieved with H₂, 5.75 J/l and 3.5%, are lower. It is shown, through a time-resolved study of the electrical discharge and spatial dynamics correlated to laser power and energy measurements, that discharge instabilities are responsible for the poor laser performance of the mixture with H₂. These instabilities, which lead to arc development, are characteristics of the discharge in Ne/SF₆. It is demonstrated for the first time that addition of a heavy hydrocarbon, such as C₂H₆, to that mixture induces the discharge stabilization so that the laser emission arises in a homogeneous active medium. This effect allows us to achieve better laser performance than with H₂. Received: 17 March 1998/Revised version: 13 July 1998