By combining ultraviolet and visible absorption and elastic light scatterin
g measurements we have studied the salt-induced aggregation kinetics of the
porphyrin t-H2Pagg in aqueous solution, The temporal evolution of the spec
tra, directly related to the time dependence of the monomer concentration a
nd the mean cluster size, shows unambiguously the presence of an early stag
e driven by a reaction limited aggregation. After a variable time (dependen
t on the salt concentration) a crossover to a diffusion-limited aggregation
regime is observed. Elastic light scattering data confirm such a result.