RESUMO
The visible absorption spectra of various substituted porphyrin compounds both in chloroform solution and as Langmuir-Blodgett (LB) solid-state films have been investigated. The porphyrin compounds examined were the Zn, Sn, Mg, and free base derivatives of 5,10,15,20-tetrakis[3,4-bis(2-ethylhexyloxy)phenyl]-21H,23H-porphine (EHO). Changes in the absorption spectra of these materials induced by their exposure to various organic compounds are reported with a view toward determining whether this is a useful approach toward an optical gas sensor.
RESUMO
A kinetic model is proposed to describe the diffusion and adsorption behavior of gas in multilayer films. Numerical solutions are attained on time scales of seconds using a finite differencing approximation to the kinetic equations. Predictions of this model are compared to experimental data for the case of NO2 diffusing through a porphyrin film. The model predicts a binding energy for the NO2 porphyrin interaction of 0.72 eV. It also predicts that for this system diffusion is the limiting factor for the adsorption response time of the film, although the recovery time is determined by both the diffusion coefficient and NO2 binding energy. Comparison with experiment gives a predicted diffusion coefficient of approximately 10(-14) m2.s-1.