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Revisiting iron oxidation chemistry in synthesis flames: Insights from a shock-tube study with intracavity laser absorption spectroscopy tracking of FeO

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DOI: 10.1016/j.jaecs.2023.100184

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Shock tube; Intracavity absorption spectroscopy; Iron oxidation; Flame synthesis

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The reaction between Fe atoms and O2 in a mixture of IPC and oxygen has been studied using a combination of ARAS and ICAS methods. FeO was found to be present at temperatures below 1400K, leading to a reassessment of rate coefficients for different Fe oxidation channels.
The reaction between Fe atoms and O2 in a mixture of iron-pentacarbonyl (IPC, 2 ppm) and oxygen (100 ppm), diluted in argon, has been studied in a shock tube behind reflected shock waves over the temperature and pressure ranges of 1050-3400 K and 0.7-2.0 bar. Time-resolved measurements of Fe and FeO have been performed simultaneously using a combination of atomic resonance absorption spectroscopy (ARAS) and intracavity laser absorption spectroscopy (ICAS) with a custom-made broadband dye laser, respectively. For ICAS, absorption features in the spectral range from 16,316 to 16,353 cm-1 have been evaluated, and the oscillator strengths for all 41 assigned ro-vibronic transitions have been expressed. For most of the experimental cases, the measured Fe and FeO traces agreed well with the mechanism reported in this work. The quantitative and highly-sensitive measurements revealed the presence of FeO at temperatures below 1400 K, leading to a reconsideration of rate coefficients for different Fe oxidation channels.

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