9–12 Sept 2024
University Oxford
Europe/London timezone

ULTRAVIOLET LASER ABSORPTION SPECTROSCOPY IN SHOCK TUBE FLOWS

12 Sept 2024, 16:15
25m
Oxford e-Research Centre (University Oxford)

Oxford e-Research Centre

University Oxford

7 Keble Rd, Oxford OX1 3QG United Kingdom
High speed facilities, flight testing and propulsion High speed facilities, flight testing and propulsion

Speaker

Maïlys Buquet

Description

  1. INTRODUCTION
    The complexity of the flowfield encountered around reentering
    vehicles poses significant problems to the design
    of spacecraft thermal protection systems. One
    large source of uncertainty is linked to thermochemical
    non-equilibrium. Ground testing is conducted to generate
    flows similar to those encountered in flight, replicating
    the essential features of non-equilibrium flows.
    One such canonical experimental setup is the shock
    tube, where a normal shock transiently passes through a
    straight tube [CB17]. Although subject to several facilityrelated
    artefacts [CMM23, CSMM22], this setup represents
    one of the most fundamental fluid mechanical
    processes, which allows the isolation of thermochemical
    non-equilibrium from other aspects of complex flowfields.
    As such, shock tubes provide the opportunity of
    studying fundamentals of thermochemical reactions for
    flight-relevant enthalpies.
    Optical diagnostics provide the ideal vehicle to interrogate
    these flows with respect to their thermochemical
    state. As one such technique, laser absorption spectroscopy
    (LAS) is seeing a rise in use due to the recent
    improvement in high-speed tunable diode lasers and
    quantum cascade lasers [SKW+19, GGD+24]. LAS targets
    the lower state of radiative transitions and can therefore
    provide absolute number density measurements of
    low-energy quantum states. If ground states are measured,
    absolute particle densities of the probed species
    can be inferred with high accuracy. Scanning absorption
    spectroscopy techniques utilise a spectrally narrow light
    source whose central wavelength is changed very rapidly.
    By scanning over an absorption line in this fashion and
    recording the transmitted light with a detector, the line
    profile and absolute absorbance are measured and can be
    utilised to infer the translational temperature and lower
    state density. Broad band light sources can be utilised as
    well, however, the absorption features need to be spectrally
    resolved by a spectrometer. In the current work, a
    broad band light source is used, as it provides an instantaneous
    snapshot of the passing shock wave and does not
    require tuning of the wavelength during the experiment.

  2. METHODOLOGY
    Shock tube flows are generated in the Oxford T6 Stalker
    Tunnel in aluminium shock tube mode [GCM22]. Optical
    measurements are taken through windows set in the
    shock tube wall, and acquisition is triggered to record
    as it passes this location. Flow conditions investigated
    in this work will consist of a set of velocities between
    5.5 km.s􀀀1 and 6.5 km.s􀀀1 [GCM22]. The laser absorption
    spectroscopy system utilises a bespoke modeless
    laser based on the work by Ewart [Ewa85]. A pulsed
    laser source provides a beam with a high degree of collimation
    that is advantageous for propagation over a long
    path, accurate steerability through the region of interest
    and efficient illumination of the spectrometer for recording
    the absorption spectrum. Laser sources, however,
    are usually characterized by a spectrum of longitudinal
    modes with frequency separation related to the laser cavity
    length. The spectral gaps between modes and their
    fluctuation in amplitude and frequency leads to difficulties
    in recording absorption spectra consisting of narrow
    spectral features. Some molecular absorption lines that
    may fall between the modes will not be recorded or distorted
    as a result of the amplitude and frequency fluctuations.
    The modeless laser, since it operates without a resonant
    cavity, is free from longitudinal mode-structure and
    provides an essentially continuous spectrum with spectral
    noise determined basically by quantum fluctuations in
    the amplified spontaneous emission from the amplifying
    medium. The unique advantage of this system is that it
    provides a tunable centre wavelength with variable bandwidth
    and a continuous spectrum that eliminates mode
    noise [SSE91, EAB+05, KE97].
    A flashlamp-pumped nanosecond Surelite I-10 Nd:YAG
    laser is used in its third harmonic mode producing radiation
    at 355 nm which is passed through a set of lenses
    to control the beam size. The Nd:YAG fundamental and
    second harmonic (1064 nm and 532 nm) are dumped in
    an enclosure outside of the Nd:YAG laser head, with
    only the third harmonic propagating into the modeless
    laser system. The third harmonic beam is separated into
    four beams by a four-faceted prism which are each absorbed
    by a dye cell at different heights [Ewa85]. The
    dye cell features a continuous flow of ethanol containing
    0.28 g.L􀀀1 of Coumarin dye. The dye produces a spectrally
    broad output at each of the four pumped locations.
    The spontaneous emission from the four pumped strips
    in the dye cell are amplified as a travelling wave by refection
    at two totally internally reflecting (TIR) prisms
    with apexes slightly displaced relative to each other. The
    dispersing prism selects a band of wavelengths from the
    fluorescence spectrum of the dye. The orientation of the
    right-hand TIR prism is used to select a band centred on
    452 nm. The output beam is subsequently frequency doubled
    in a critically phase-matched crystal of BBO (Beta
    Barium Borate) to 226 nm with a bandwidth (FWHM)
    of approximately 2 nm. This ultra-violet beam is separated
    from the fundamental at 452 nm using a Pellin-
    Broca prims and directed to the shock tube.
    Once the beam is produced with the aforementioned
    spectral properties, it is passed through a system of turning
    mirrors and relay lenses to the side of the T6 tunnel.
    At this location it is expanded and collimated by a twolenses
    system containing a cylindrical and a spherical
    lens, resulting in a laser sheet. This sheet is aligned with
    the field of view of a telecentric imaging system. As the
    shock wave travel through this field of view, the laser is
    activated and partially absorbed by the nitric oxide in the
    flow. The laser sheet will be arranged in such a way that it
    covers the freestream, non-equilibrium region and equilibrium
    region behind the shock front. The transmitted
    radiation of the sheet is imaged onto the entrance slit of
    the spectrometer. Hence, the resulting spectral image corresponds
    to a spatially resolved image along one dimension.
    This way, the absorbance can be simultaneously
    measured at different locations across the shock wave, resulting
    in a resolution of the non-equilibrium layer. The
    data acquired in this way will be used to infer NO number
    densities and excitation temperatures through spectral
    fitting methods.

  3. RESULTS
    The full paper will present the data of the currently ongoing
    test campaign and will contain setup, calibration and
    post-processing. Raw absorbance data will be shown, as
    well as the post-processed properties of nitric oxide in the
    shock layer. The post-processing will be undertaken by
    comparing the measured absorbance to a computational
    model which simulates the absorption through a hightemperature
    gas. This will allow the determination of
    nitric oxide ground-state densities, as well as vibrational
    and rotational temperature.

Summary

A flashlamp-pumped nanosecond Surelite I-10 Nd:YAG
laser is used in its third harmonic mode producing radiation
at 355 nm which is passed through a set of lenses
to control the beam size. The Nd:YAG fundamental and
second harmonic (1064 nm and 532 nm) are dumped in
an enclosure outside of the Nd:YAG laser head, with
only the third harmonic propagating into the modeless
laser system. The third harmonic beam is separated into
four beams by a four-faceted prism which are each absorbed
by a dye cell at different heights [Ewa85]. The
dye cell features a continuous flow of ethanol containing
0.28 g.L􀀀1 of Coumarin dye. The dye produces a spectrally
broad output at each of the four pumped locations.
The spontaneous emission from the four pumped strips
in the dye cell are amplified as a travelling wave by refection
at two totally internally reflecting (TIR) prisms
with apexes slightly displaced relative to each other. The
dispersing prism selects a band of wavelengths from the
fluorescence spectrum of the dye. The orientation of the
right-hand TIR prism is used to select a band centred on
452 nm. The output beam is subsequently frequency doubled
in a critically phase-matched crystal of BBO (Beta
Barium Borate) to 226 nm with a bandwidth (FWHM)
of approximately 2 nm. This ultra-violet beam is separated
from the fundamental at 452 nm using a Pellin-
Broca prims and directed to the shock tube.
Once the beam is produced with the aforementioned
spectral properties, it is passed through a system of turning
mirrors and relay lenses to the side of the T6 tunnel.
At this location it is expanded and collimated by a twolenses
system containing a cylindrical and a spherical
lens, resulting in a laser sheet. This sheet is aligned with
the field of view of a telecentric imaging system. As the
shock wave travel through this field of view, the laser is
activated and partially absorbed by the nitric oxide in the
flow. The laser sheet will be arranged in such a way that it
covers the freestream, non-equilibrium region and equilibrium
region behind the shock front. The transmitted
radiation of the sheet is imaged onto the entrance slit of
the spectrometer. Hence, the resulting spectral image corresponds
to a spatially resolved image along one dimension.
This way, the absorbance can be simultaneously
measured at different locations across the shock wave, resulting
in a resolution of the non-equilibrium layer. The
data acquired in this way will be used to infer NO number
densities and excitation temperatures through spectral
fitting methods.

Primary author

Maïlys Buquet

Co-authors

Alex Glenn (Oxford University DPhil Student) Prof. Benjamin A. O. Williams (Oxford University) Dr Laurent M. Le Page (Oxford University) Prof. Matthew McGilvray (Oxford University) Prof. Paul Ewart (Oxford University) Dr Tobias Hermann (Oxford University)

Presentation materials