We have compared the hydration behavior of single carbon particles tha
t have been treated by exposure to gaseous H2SO4 with that of untreate
d particles. Untreated carbon particles did not hydrate as the relativ
e humidity varied from 0 to 80% at 23-degrees-C. In contrast, treated
particles hydrated under subsaturation conditions; mass increases of u
p to 30% were observed. The mass increase is consistent with sulfuric
acid equilibration with the ambient relative humidity in the presence
of inert carbon. For the samples studied, the average amount of adsorb
ed acid was 14% +/- 6% by weight, which corresponds to a surface cover
age of approximately 0.1 monolayer. The mass fraction of surface-adsor
bed acid is comparable to the soluble mass fraction observed by Whitef
ield et al. (1993) in jet aircraft engine aerosols. Estimates indicate
this mass fraction corresponds to 0.1% of the available SO2 exiting a
n aircraft engine ending up as H2SO4 on the carbon aerosol. If this he
terogeneous process occurs early enough in the exhaust plume, it may c
ompete with homogeneous nucleation as a mechanism for producing sulfur
ic acid rich aerosols.