2017
DOI: 10.2514/1.j055371
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Finite-Rate Oxidation Model for Carbon Surfaces from Molecular Beam Experiments

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Cited by 67 publications
(32 citation statements)
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“…Furthermore, the pulsed nature of the molecular beam led to in-depth studies of the time-varying aspects of the experiments [27] [28]. In contrast, the original model by Poovathingal et al [20] [21], assumed that the reaction products (and their relative probabilities) observed during the beam pulse would be the same as those observed if the beam were continuously operating, and the unsteady details of the measurements between pulses were not relevant to formulate an ablation model. It was also observed experimentally that the product flux (leaving the surface) captured by the mass spectrometer was not the same at high and low temperatures, despite the same molecular beam conditions (i.e., the same beam flux).…”
Section: New Molecular Beam Data and Relevance To Hypersonic Ablationmentioning
confidence: 99%
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“…Furthermore, the pulsed nature of the molecular beam led to in-depth studies of the time-varying aspects of the experiments [27] [28]. In contrast, the original model by Poovathingal et al [20] [21], assumed that the reaction products (and their relative probabilities) observed during the beam pulse would be the same as those observed if the beam were continuously operating, and the unsteady details of the measurements between pulses were not relevant to formulate an ablation model. It was also observed experimentally that the product flux (leaving the surface) captured by the mass spectrometer was not the same at high and low temperatures, despite the same molecular beam conditions (i.e., the same beam flux).…”
Section: New Molecular Beam Data and Relevance To Hypersonic Ablationmentioning
confidence: 99%
“…It was also observed experimentally that the product flux (leaving the surface) captured by the mass spectrometer was not the same at high and low temperatures, despite the same molecular beam conditions (i.e., the same beam flux). Since reaction products were observed to leave the surface thermally, the model by Poovathingal et al [20] [21] assumed that the product flux not captured by the detector had similar chemical composition as the product flux that was captured by the detector. In contrast, the model by Swaminathan-Gopalan et al [27] assumed that the product flux not captured by the detector was entirely composed of CO and that this CO was not counted because it left the surface between beam pulses.…”
Section: New Molecular Beam Data and Relevance To Hypersonic Ablationmentioning
confidence: 99%
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