Laser-Induced Fluorescence for Temperature and Density of CN and CO in the Boundary Layer of Graphite Ablation in an Inductively-Coupled Plasma Torch Plume

被引:0
作者
Murray, John S. [1 ]
Clemens, Noel T. [1 ]
机构
[1] Univ Texas Austin, Dept Aerosp Engn & Engn Mech, Claire Cockrell Williams Centennial Chair Engn, Austin, TX 78712 USA
来源
AIAA SCITECH 2024 FORUM | 2024年
关键词
CARBON-MONOXIDE; 2-PHOTON ABSORPTION; QUENCHED LIFETIME; EXCITATION; FEMTOSECOND; HYDROGEN; SCHEMES; FLAMES;
D O I
暂无
中图分类号
V [航空、航天];
学科分类号
08 ; 0825 ;
摘要
Laser-Induced Fluorescence (LIF) is used to study the cyano radical (CN) and carbon monoxide (CO) in the reacting boundary layer of an ablating carbon graphite sample exposed to high temperature air at atmospheric pressure. The CN radical is an important contributor to the radiative heat transfer experienced by a hypersonic vehicle, and there is uncertainty in the literature regarding the chemical kinetic parameters of its formation. CO, on the other hand, is the dominant product of surface oxidation for carbon ablators. The air plume is generated using the 50 kW Inductively-Coupled Plasma (ICP) torch at The University of Texas at Austin, which operates at a temperature of about 6000 K and delivers a cold-wall heat flux of approximately 130 W/cm(2). Quantitative LIF of COwas obtained using a photoionization-limited (PI-limited), two-photon LIF technique, while the CN LIF results are purely qualitative. The CO mole fraction peaked at 0.25 approximately 100 mu m from the graphite surface and decreased monotonically away from the sample to less than 0.05 at a distance of 3 mm. The temperature profile in the boundary layer - obtained from a two-line intensity ratio - varied from the freestream temperature of 6000 K about 1.5 mm from the sample to 3200 K about 100 mu m away. From the qualitative CN LIF, we see that the dominant mechanism of CN production appears to be in the gas-phase, with relatively little CN LIF signal coming from near the surface.
引用
收藏
页数:12
相关论文
共 45 条
[1]   MEASUREMENT OF THE COLLISION-QUENCHED LIFETIME OF CO MOLECULES IN A FLAME AT ATMOSPHERIC-PRESSURE [J].
AGRUP, S ;
ALDEN, M .
CHEMICAL PHYSICS LETTERS, 1992, 189 (03) :211-216
[2]   MEASUREMENTS OF THE COLLISIONALLY QUENCHED LIFETIME OF CO IN HYDROCARBON FLAMES [J].
AGRUP, S ;
ALDEN, M .
APPLIED SPECTROSCOPY, 1994, 48 (09) :1118-1124
[3]   Development of a Nonequilibrium Finite-Rate Ablation Model for Radiating Earth Reentry Flows [J].
Alba, Christopher R. ;
Greendyke, Robert B. ;
Marschall, Jochen .
JOURNAL OF SPACECRAFT AND ROCKETS, 2016, 53 (01) :98-120
[4]   APPLICATIONS OF 2-PHOTON ABSORPTION FOR DETECTION OF CO IN COMBUSTION GASES [J].
ALDEN, M ;
WALLIN, S ;
WENDT, W .
APPLIED PHYSICS B-PHOTOPHYSICS AND LASER CHEMISTRY, 1984, 33 (04) :205-212
[5]   Picosecond excitation for reduction of photolytic effects in two-photon laser-induced fluorescence of CO [J].
Brackmann, Christian ;
Sjoholm, Johan ;
Rosell, Joakim ;
Richter, Mattias ;
Bood, Joakim ;
Alden, Marcus .
PROCEEDINGS OF THE COMBUSTION INSTITUTE, 2013, 34 :3541-3548
[6]   Modeling of Carbon Monoxide Two-Photon Laser-Induced Fluorescence (LIF) Spectra at High Temperature and Pressure [J].
Carrivain, Olivier ;
Orain, Mikael ;
Dorval, Nelly ;
Morin, Celine ;
Legros, Guillaume .
APPLIED SPECTROSCOPY, 2020, 74 (06) :629-644
[7]   Experimental Spectroscopic Studies of Carbon Monoxide (CO) Fluorescence at High Temperatures and Pressures [J].
Carrivain, Olivier ;
Orain, Mikael ;
Dorval, Nelly ;
Morin, Celine ;
Legros, Guillaume .
APPLIED SPECTROSCOPY, 2017, 71 (10) :2353-2366
[8]   SEMIQUANTITATIVE LASER-INDUCED FLUORESCENCE IN FLAMES [J].
CROSLEY, DR .
COMBUSTION AND FLAME, 1989, 78 (01) :153-167
[9]   COLLISIONAL EFFECTS ON LASER-INDUCED FLUORESCENCE FLAME MEASUREMENTS [J].
CROSLEY, DR .
OPTICAL ENGINEERING, 1981, 20 (04) :511-521
[10]   Two-photon excitation cross section of the B ← X(0,0) band of CO measured by direct absorption [J].
Di Rosa, MD ;
Farrow, RL .
JOURNAL OF THE OPTICAL SOCIETY OF AMERICA B-OPTICAL PHYSICS, 1999, 16 (11) :1988-1994