This poster presents an overview of the ability of mineral nanoparticles to alter transport properties of polymeric materials for membrane applications. Nanoparticle filled polymers have been prepared that exhibit over an order of magnitude higher light gas (i.e., carbon dioxide, nitrogen, methane, hydrogen etc.) permeability with little or no change in selectivity relative to that of the unfilled polymer. This phenomena has been observed in a broad range of polymeric materials, from high free volume stiff-chain polyacetylenes and crosslinked poly(ethylene oxide) to commodity materials such as 1,2-polybutadiene and poly(ethylene-co-1-octene). The degree of permeability enhancement is polymer and particle loading dependent, and our studies include a wide range of polymer and particle chemistries, including situations where the polymer and nanoparticles undergo chemical reactions. Moreover, nanocomposite light gas permeability and selectivity are highly dependent on nanoparticle surface chemistry. The nanoparticles are nonporous and are primarily from the metal oxide family (magnesia, silica, titania, etc.). These nanocomposites have been characterized using light gas sorption and permeation to monitor gas transport properties. Particle dispersion in the bulk has been determined using atomic force microscopy.