The adsorption of Athabasca and Cold Lake C-7-asphaltenes on stainless steel (304L), iron, and aluminum powders was measured using UV-vis spectrophotometry. The effects of resins, temperature, and n-heptane-to-toluene ratio were also investigated. In all cases, Langmuir (type 1) isotherms were observed, indicating that asphaltenes saturated the available surface area for adsorption. The saturation adsorptions of the asphaltenes on metals (0.25-2.7 mg/m(2)) were of the same order of magnitude as adsorption of asphaltenes on minerals. The saturation adsorptions were less than the monolayer surface coverage observed on water-in-hydrocarbon emulsion interfaces, indicating that there are a limited number of adsorption sites on the metals. Higher molar saturation adsorptions were observed for resins and low molar mass asphaltenes, suggesting that adsorption was limited by the morphology of the metal surface. In general, higher mass saturation adsorptions were observed when asphaltenes self-associated to greater extents and consequently larger molecules adsorbed on the surface.