posted on 2000-04-15, 00:00authored byJohn M. Veranth, Kevin R. Smith, Autumn A. Hu, JoAnn S. Lighty, Ann E. Aust
The observed iron mobilization rate from size-fractionated coal fly ash is consistent with
the model predictions for a limiting case of mass transfer where the dominant resistance is
diffusion through a layer of depleted solid between the surface of spherical particles and a
shrinking core of unreacted material. The rate of mobilization of iron from coal fly ash under
physiologically relevant conditions in vitro was previously shown to depend on the size of the
ash particles and on the source of the coal, and these in vitro measurements have been shown
to correlate with indirect measurements of excess iron in cultured cells. Existing iron
mobilization data were compared to mathematical models for mass transfer and chemical
reaction in solid−liquid heterogeneous systems. Liquid-phase diffusion resistance can be ruled
out as the rate-limiting mechanism for iron mobilization as the model predictions for this case
are clearly inconsistent with the measurements. Other plausible hypotheses, such as a rate
limited by a heterogeneous surface reaction, cannot be conclusively ruled out by the available
data. These mathematical analysis methods are applicable to the design of future experiments
to determine the rate-limiting mechanism for the mobilization of iron and of other transition
metals from both ambient air samples and surrogates for major sources of particulate air
pollution.