In the present study, the photolysis of carbofuran has been undertaken under sunlight conditions and at the surface of model supports such as clay films and different soils collected from two different sites in Morocco (Tirs and Dahs). In all conditions, an efficient degradation occurred owing to direct light absorption and also to photoinduced processes involving either clays or natural organic matter moities. On kaolin films, the photodegradation kinetics appears to follow a first-order process that clearly depends on the film thickness. The diffusion of carbofuran from the lower part to the illuminated surface was found to be negligible when compared to the photolysis process within the range of 20–70 μm. Thus, the photolysis rate constant at the surface of the solid support, k 0, was evaluated to be 7.0 × 10−3 min−1. Under these experimental conditions, the quantum yield was found equal to 2.1 × 10-4. On soil surfaces, the disappearance rate constant was mainly attributed to photoinduced processes arising from natural organic matter. From the analytical point of view, the products were formed through (1) hydroxylation on the aromatic ring, (2) homolytic scission of the carbamate C–O bond leading to radical species formation, and (3) photohydrolysis of the carbamate C–O bond.