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Soot Formation in Laminar Premixed Ethylene/Air Flames at Atmospheric Pressure. Appendix G

TLDR
In this paper, the surface growth rate of premixed ethylene/air flames with C/O ratios of 0.78-0.98 was found to be due to reduced H atom concentrations as temperatures decrease as a result of radiative heat losses.
Abstract
Abstract Soot formation was studied within laminar premixed ethylene/air flames (C/O ratios of 0.78–0.98) stabilized on a flat-flame burner operating at atmospheric pressure. Measurements included soot volume fractions by both laser extinction and gravimetric methods, temperatures by multiline emission, soot structure by thermophoretic sampling and transmission electron microscopy, major gas species concentrations by sampling and gas chromatography, concentrations of condensable hydrocarbons by gravimetric sampling, and velocities by laser velocimetry. These data were used to find soot surface growth rates and primary soot particle nucleation rates along the axes of the flames. Present measurements of soot surface growth rates were correlated successfully by predictions based on typical hydrogen-abstraction/carbon-addition (HACA) mechanisms of Frenklach and co-workers and Colket and Hall. These results suggest that reduced soot surface growth rates with increasing residence time seen in the present and other similar flames were mainly caused by reduced rates of surface activation due to reduced H atom concentrations as temperatures decrease as a result of radiative heat losses. Primary soot particle nucleation rates exhibited variations with temperature and acetylene concentrations that were similar to recent observations for diffusion flames; however, nucleation rates in the premixed flames were significantly lower than in the diffusion flames for reasons that still must be explained. Finally, predictions of yields of major gas species based on mechanisms from both Frenklach and co-workers and Leung and Lindstedt were in good agreement with present measurements and suggest that H atom concentrations (relevant to HACA mechanisms) approximate estimates based on local thermodynamic equilibrium in the present flames.

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Citations
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References
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PREMIX :A F ORTRAN Program for Modeling Steady Laminar One-Dimensional Premixed Flames

TL;DR: In this paper, a Fortran computer program that computes species and temperature profiles in steady-state burner-stabilized and freely propagating laminar flames is described.
Journal ArticleDOI

Reaction mechanism of soot formation in flames

TL;DR: In this paper, chemical reactions and physical processes responsible for the formation of polycyclic aromatic hydrocarbons and soot in hydrocarbon flames are reviewed, focusing on major elements in the present understanding of the phenomena, clarification of concepts central to the present state of the art, and a summary of new results.
Journal ArticleDOI

Kinetic modeling of soot formation with detailed chemistry and physics: laminar premixed flames of C2 hydrocarbons

TL;DR: In this article, an updated detailed chemical kinetic model for soot formation is presented, which combines recent developments in gas phase reactions, aromatic chemistry, soot particle coagulation, and particle aggregation, and develops a new submodel for surface growth.
Journal ArticleDOI

Optical Constants of Soot and Their Application to Heat-Flux Calculations

TL;DR: In this article, the spectral absorption coefficient and the total emissivities of soot suspensions were calculated for the room temperature optiaI.1 and 2.5-1O.
Journal ArticleDOI

A simplified reaction mechanism for soot formation in nonpremixed flames

TL;DR: In this paper, a reaction mechanism for soot formation in non-premixed flames is proposed and tested for different flame configurations and fuels, and the mechanism is combined with detailed and simplified gas phase chemistry for ethylene and methane flames respectively.
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