Reactive and inelastic scattering dynamics of hyperthermal O and O2 from a carbon fiber network

被引:4
|
作者
Poovathingal, Savio J. [1 ]
Qian, Min [2 ]
Murray, Vanessa J. [3 ]
Minton, Timothy K. [4 ]
机构
[1] Dept Mech Engn, 287 Ralph G Anderson Bldg, Lexington, KY 40506 USA
[2] East China Univ Sci & Technol, Sch Sci, Dept Phys, Shanghai 200237, Peoples R China
[3] Montana State Univ, Dept Chem & Biochem, Bozeman, MT 59717 USA
[4] Univ Colorado Boulder, Ann & HJ Smead Dept Aerosp Engn Sci, 3775 Discovery Dr, Boulder, CO 80303 USA
关键词
Carbon oxidation; Carbon ablation; Carbon preform; Gas-surface interactions; Molecular beam scattering; ATOMIC OXYGEN; GRAPHITE OXIDATION; CHAR GASIFICATION; VITREOUS CARBON; BEAM SCATTERING; MOLECULAR-BEAMS; LIQUID SURFACES; KINETICS; DIOXIDE; TEMPERATURE;
D O I
10.1016/j.carbon.2021.07.009
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Pulsed beams containing O and O-2 with incident velocities of similar to 7900 m s(-1) were directed at a carbon fiber preform network (FiberForm) at temperatures in the range, 1023-1823 K, and the products that scattered from the network were detected with a rotatable mass spectrometer as a function of their velocities and scattering angles. A beam containing pure Ar atoms was also directed at the network, allowing multiple-bounce effects in the absence of reaction to be characterized. Scattered O, O-2, and Ar exhibited the dynamical characteristics of impulsive (non-thermal) scattering and thermal desorption (TD). On the other hand, CO and CO2 exhibited only TD dynamics. The fluxes of all products were quantified as a function of sample temperature and, for two focus temperatures, as a function of scattering angle. CO was the dominant reactive product. A temperature dependent hysteresis in the CO flux was quantified, and a comparison was made between the hysteresis on the carbon fiber network and on a planar vitreous carbon surface. The new results may be used to increase the fidelity of oxygen-carbon ablation models for hypersonic flight. (C) 2021 Published by Elsevier Ltd.
引用
收藏
页码:277 / 290
页数:14
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