RESUMEN
A burst-mode nitrogen (N2) picosecond vibrational coherent anti-Stokes Raman scattering (ps-VCARS) system is presented for accurate flame thermometry at 100 kHz repetition rate. A frequency-tripled ps burst-mode laser is used to pump a custom optical parametric generator/amplifier to produce 607 nm broadband Stokes pulses with 120cm-1 bandwidth, along with a narrowband 532 nm pump/probe beam. A simultaneous shot-to-shot nonresonant background (NRB) measurement is implemented to account for Stokes spectral profile and beam overlap fluctuations. The 100 kHz ps-VCARS data are benchmarked in a near-adiabatic CH4/air Hencken calibration flame with an accuracy of 1.5% and precision of 4.7% up to peak flame temperatures. The use of N2 VCARS and simultaneous NRB measurements enables high-speed thermometry for a wide range of fuels and combustion applications.
RESUMEN
10-kHz hydroxyl radical (OH) two-color planar laser-induced fluorescence (TC-PLIF) thermometry was demonstrated with a single burst-mode optical parametric oscillator (OPO) and a single camera. A fast, dual-wavelength switched seed laser enabled a high-energy, high-repetition-rate burst-mode laser to generate two 10-kHz pulse trains at wavelengths of ${\sim}{354.8}\;{\rm nm}$. The two pulse trains are colinear with 3 µs time interval between the pulse pairs. The injection-seeded OPO efficiently converts the burst-mode laser output to 285.62 and 285.67 nm to excite the ${Q}_2({12})$ and ${P}_1({8})$ OH transitions. PLIF images were collected from each of the two excitation transitions, and intensity ratios from the images were used to determine local temperatures. The development of fast, dual-wavelength switching, burst-mode OPO technology significantly reduces the experimental complexity of the high-speed TC-PLIF thermometry and simplifies its implementation in harsh combustion and flow test facilities.
RESUMEN
Nanosecond electronic-resonance-enhanced coherent anti-Stokes Raman scattering (ERE-CARS) is evaluated for the measurement of formaldehyde (CH2O) concentrations in reacting and nonreacting conditions. The three-color scheme utilizes a 532 nm pump beam and a scanned Stokes beam near 624 nm for Raman excitation of the C-H symmetric stretch (ν1) vibrational mode; further, a 342 nm resonant probe is tuned to produce the outgoing CARS signal via the 101403 vibronic transition between the ground (X~1A1) and first excited (A~1A2) electronic states. This allows detection of CH2O at concentrations as low as 9×1014molecules/cm3 (55 parts per million) in a calibration cell with CH2O and N2 at 1 bar and 450 K with 3% uncertainty. The measurements show a quadratic dependence of the signal with CH2O number density. Pressure scaling experiments up to 11 bar in the calibration cell show an increase in signal up to 8 bar. We study pressure dependence up to 11 bar and further apply the technique to characterize the CH2O concentration in an atmospheric premixed dimethyl ether/air McKenna burner flame, with a maximum concentration uncertainty of 11%. This approach demonstrates the feasibility for spatially resolved measurements of minor species such as CH2O in reactive environments and shows promise for application in high-pressure combustors.
RESUMEN
A molecular tagging method for velocity measurements in reacting environments such as propulsion devices and high-temperature combustion-assisted wind tunnels is described. The method employs a femtosecond (write) laser to photodissociate H2O, a common combustion product, into a locally high concentration of OH radicals. These radicals are tracked by planar laser-induced fluorescence (PLIF) from the A2Σ-X2Π (1-0) vibrational band excited by a time-delayed 284 nm (read) laser sheet. As a variant of hydroxyl tagging velocimetry, the source laser can also be used to dissociate nitrogen for femtosecond laser electronic excitation tagging velocimetry to mark the time-zero location of the write laser for velocimetry in non-reacting regions using the same imaging system without OH PLIF. The OH tracer lifetime is studied in a hydrogen-air Hencken burner operating at Φ=0.5-1.8 to evaluate the tracking capability for velocimetry over a range of conditions. Effects of changing read laser wavelength, excitation energy, and influence of background flame emission are also studied. The data processing methodology and results are described for tracking displacements with 9-25 µm uncertainty in a hydrogen diffusion flame. This method presents several advantages in operational convenience and availability of laser sources, and it provides an avenue for improvements in the repetition rate, precision, and applicability over previously demonstrated hydroxyl tagging schemes.