Evolution of maturity levels of the particle surface and bulk during soot growth and oxidation in a flame |
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Authors: | K. O. Johansson F. El Gabaly P. E. Schrader M. F. Campbell |
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Affiliation: | 1. Combustion Research Facility, Sandia National Laboratories, Livermore, California, USA;2. Materials Physics Department, Sandia National Laboratories, Livermore, California, USA |
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Abstract: | We performed a study of the evolution of soot composition and fine structure, i.e., maturity level, in an atmospheric ethylene-air diffusion flame. We used laser-induced incandescence (LII) to provide information about maturity level of the bulk primary particle and X-ray photoelectron spectroscopy (XPS) to provide complementary information about particle-surface-maturity level. The results demonstrate that the bulk material and the particle surface evolve separately in the flame. Increased soot-maturity level is associated with increased long-range order of the particle fine structure. This increased order leads to an increase in the absorption cross-section in the visible and near-infrared and a shift of the absorption to longer wavelengths with increasing maturity level of the bulk particle. These trends result in a decrease in the dispersion exponent (?) and increase in the absorption cross-section scaling factor (?), as inferred from LII measurements. LII measurements demonstrate that bulk-maturity level increases with height-above-the-burner (HAB) until it reaches a plateau in the center of the flame at the maximum in the soot volume fraction. Bulk-maturity level only slightly decreases as soot is oxidized at larger HABs. Increased maturity level also leads to an increase in long-range sp2 hybridization. XPS measurements of the sp2/defect ratio demonstrate an increase in soot surface-maturity level with increasing HAB, but the surface-maturity level increases more gradually with HAB than the bulk-maturity level. Whereas the bulk-fine-structure order decreases slightly in the oxidation region, the surface order decreases dramatically, indicating that oxidation occurs preferentially at the surface under these conditions.Copyright © The Authors. Published with license by American Association for Aerosol Research |
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Keywords: | Thomas Kirchstetter |
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