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A shock-tube facility consisting of two, single-pulse shock tubes for the study of fundamental processes related to gas-phase chemical kinetics and the formation and reaction of solid and liquid aerosols at elevated temperatures is described. Recent upgrades and additions include a new high-vacuum system, a new gas-handling system, a new control system and electronics, an optimized velocity-detection scheme, a computer-based data acquisition system, several optical diagnostics, and new techniques and procedures for handling experiments involving gas/powder mixtures. Test times on the order of 3 ms are possible with reflected-shock pressures up to 100 atm and temperatures greater than 4000 K. Applications for the shock-tube facility include the study of ignition delay times of fuel/oxidizer mixtures, the measurement of chemical kinetic reaction rates, the study of fundamental particle formation from the gas phase, and solid-particle vaporization, among others. The diagnostic techniques include standard differential laser absorption, FM laser absorption spectroscopy, laser extinction for particle volume fraction and size, temporally and spectrally resolved emission from gas-phase species, and a scanning mobility particle sizer for particle size distributions. Details on the set-up and operation of the shock tube and diagnostics are given, the results of a detailed uncertainty analysis on the accuracy of the test temperature inferred from the incident-shock velocity are provided, and some recent results are presented.

A study of the structure and dynamics of the hydronium ion by high resolution infrared laser spectroscopy. III. The ν3 band of D3O+ J. Chem. Phys. 92, 3257 (1990); 10.1063/1.457884 Infrared spectroscopy of carboions. V. Classical vs nonclassical structure of protonated acetylene C2H+ 3 J. Chem. Phys. 91, 5139 (1989); 10.1063/1.457612 Infrared spectroscopy of carboions. IV. The A 2Π u -X 2Σ+ g electronic transition of C− 2 J. Chem. Phys. 89, 129 (1988); 10.1063/1.455731Infrared spectra of carboions. II. ν3 band of acetylene ion C2H+ 2(2Π u )

The infrared spectra of the band of the 2Π–2Π asymmetric hydrogen stretching vibration in the three isotopic acetylene ions C2H2+ (ν3), 13C2H2+ (ν3), and DCCH+ (ν1) have been observed and analyzed. The high resolution infrared spectra were recorded using a difference-frequency laser spectrometer as the tunable coherent infrared source probing an ac glow discharge. Velocity modulation, noise subtraction, and unidirectional multipassing of the infrared beam through the discharge cell provided high sensitivity. C2H2+ was produced in a gas mixture of H2, He, and either CH4 or C2H2, with a total pressure of ≊7 Torr in multiple-inlet–outlet air-, water-, and liquid-nitrogen-cooled discharge tubes; C2H2 freezing precluded its use in liquid-N2-cooled discharges. Complicated by a strong perturbation whose maximum occurred at N′=15 for F1 and N′=14 for F2, the assignment of the spectrum of normal C2H2+ was made possible by (1) fortuitous discharge conditions which provided unambiguous discrimination of C2H2+ lines from among concurrent CH3+ and C2H3+ lines, and (2) fitting the ground state combination differences. Sufficiently high N transitions were observed where Λ doubling was evident. The average bond lengths rz(CH)=1.077 (5) Å and rz(CC)=1.257 (8) Å were calculated from the spectroscopic constants determined from nonlinear least-squares fitting. Vibration–rotation interactions, the Renner–Teller interaction of perturbing states, plasma chemistry, and the relevance of the work in astrophysics are discussed.

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