Suspensions of a variety of different aluminum oxides have previously been shown to require very high concentrations of chloride and nitrate anions (>0.5 M) to induce rapid aggregation. This high stability has been accredited to the presence of surface forces considered to be due to the formation of highly charged Al 13 polymeric species at slightly acidic pH's and aluminum oxyhydroxide gel formation under alkaline conditions. The effect of this stability on the structure of the resulting aggregates is investigated here using wellestablished static light-scattering techniques. Power law behavior of scattered light intensity as a function of scattering wave vector is observed in all cases and is suggestive of fractal structure. The fractal dimensions obtained fall within the expected range of 1.8 to 2.3 observed for colloidal aggregates but do not appear to follow the typical observations for colloids destabilized by indifferent electrolytes where lower fractal dimensions are associated with rapid (diffusion-limited) aggregation and higher fractal dimensions with slower (reaction-limited) aggregation. Indeed, relatively constant fractal dimensions (2.10 to 2.25) are observed over the range of salt concentrations at which the slow to rapid aggregation rate transformation occurs with, if anything, a slightly higher fractal dimension observed for higher aggregation rates. The presence of specifically binding sulfate anions appears to negate the strong near-distance repulsive forces leading to rapid aggregation at low (1 to 2 mM) sulfate concentrations. Significantly lower fractal dimensions (1.85 to 1.91) are observed for aggregates formed by destabilization using sulfate ions than obtained when chloride or nitrate are used with, again, an apparent slight increase in fractal dimension upon increasing aggregation rate.