Abstract

A laminar, coannular, ethylene/air nonpremixed flame doped with ferrocene additive is employed toaddress the fundamental question of how iron becomes incorporated into the carbonaceous soot phase, thus interfering with the soot formation processes. The structure and chemical composition of individual aggregates are characterized with respect to flame coordinates via a combination of thermophoretic sampling, transmission electron microscopy, and energy dispersive spectrometry. Soot aggregate microstructure clearly reveals iron occlusion, as well as stratification of soot layers overthe occluded phase. The study provides physical evidence that the soot and iron compounds combine in the flame to form a hybrid (inhomogeneous) particulate phase. The reported observations are consistent with the hypothesis that ferrocene decomposes early in the combustion process and before the onset of soot particle inception, thus forming a fine aerosol for the subsequent deposition of carbonaceous substances. Examination of a series of inhomogeneous soot aggregates shows that the flame aerosol composition varies with flame coordinates. In particular, aggregates transported in the soot annulus near the luminous flame front are primarily composed of carbon and oxygen, with traces of iron finely dispersed through the aggregate matrix. On the other hand, carbonaceous soot transported at low heights and near the flame axis contains iron in its elemental form. Finally, soot aggregates in all other areas of the flame contain both iron and oxygen, thus implying the possible presence of iron oxides within the carbonaceous matrix.

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