The present disclosure describes an evaporative emission control canister system that includes: one or more canisters comprising at least one vent-side particulate adsorbent volume comprising a particulate adsorbent having microscopic pores with a diameter of less than about 100 nm; macroscopic pores having a diameter of about 100 - 100,000 nm; and a ratio of a volume of the macroscopic pores to a volume of the microscopic pores that is greater than about 150%, and having a retentivity of about 1.0 g/dL or less. The system may further include a high butane working capacity adsorbent. The disclosure also describes a method for reducing emissions in an evaporative emission control system.

There is provided a structurally stable monolith substrate, suitable to provide carbon dioxide capture structure for removing carbon dioxide from air, having two major opposed surfaces, and further having a plurality of longitudinal channels extending between and opening through the two major opposed surfaces of the structurally stable monolith substrate; and a macroporous coating, adhered to the interior wall surfaces of the longitudinal channels, comprising an adherent, coating formed of cohered, compact mesoporous particles each being formed of a material that is compatible with the material forming the underlying substrate structure so as to become adherent thereto when coated. The mesoporous particles are capable of supporting in their mesopores a sorbent for CO.sub.2 There is also provided a method for forming the monolith and a system for utilizing the monolith as part of a CO.sub.2 capture structure, within the system, to remove CO.sub.2 from the atmosphere.

A method of fabrication of a porous polymer aerogel amine material includes preparing a solution comprising at least a solvent, amine monomers having protecting groups, one or more crosslinkers, and one or more radical initiators, heating the solution to promote polymerization and to produce a polymerized material, performing solvent exchange with the polymerized material, causing a deprotection reaction in the polymerized material to remove the protecting groups to produce a deprotected material, soaking and rinsing the deprotected material to remove excess reagents and any byproducts of the deprotection reaction, and drying the deprotecting material to produce the amine sorbent. A system to separate CO.sub.2 from other gases has a polymer porous aerogel sorbent having greater than 5 wt % of amine containing vinyl monomers integrated into a polymer backbone, and the amine containing vinyl monomers may have a molecular weight of less than 100 g/mol.

A method for making a titania-polymer nanocomposite by simultaneously forming TiO.sub.2 nanoparticles in situ from a TiO.sub.2 precursor in the presence of urea and interfacially polymerizing polyamide precursors thereby producing a titania-polymer nanocomposite. A titania-polymer nanocomposite made by this method. A method for removing a dye or metal from water comprising contacting contaminated water with the titania-polymer nanocomposite.

An aminated siliceous adsorbent, which is the reaction product of dried acidified rice husk ash having disordered mesopores and an amino silane, wherein amine functional groups are present on an external surface and within the mesopores of the dried acidified rice husk ash, and wherein the aminated siliceous adsorbent has a carbon content of 24 to 30 wt. %, based on a total weight of the aminated siliceous adsorbent. A method of making the aminated siliceous adsorbent and a method of capturing CO.sub.2 from a gas mixture with the aminated siliceous adsorbent.

The present invention relates to novel sulfur-doped carbonaceous porous materials. The present invention also relates to processes for the preparation of these materials and to the use of these materials in applications such as gas adsorption, mercury and gold capture, gas storage and as catalysts or catalyst supports.

A method for making a titania-polymer nanocomposite by simultaneously forming TiO.sub.2 nanoparticles in situ from a TiO.sub.2 precursor in the presence of urea and interfacially polymerizing polyamide precursors thereby producing a titania-polymer nanocomposite. A titania-polymer nanocomposite made by this method. A method for removing a dye or metal from water comprising contacting contaminated water with the titania-polymer nanocomposite.

A capture mass for heavy metals, in particular mercury, contained in a gaseous or liquid feed, said mass comprising: copper which is present at least in part in the sulphide form, Cu.sub.xS.sub.y, a porous support based on alumina; characterized in that said porous support has a total pore volume (TPV) in the range 0.8 to 1.5 cm.sup.3/g, a mesopore volume (V.sub.6 nm-100 nm) in the range 0.5 to 1.3 cm.sup.3/g, and a macropore volume (V.sub.100 nm) in the range 0.33 to 0.45 cm.sup.3/g, it being understood that the ratio between the mesopore volume and the macropore volume (V.sub.6 nm-100 nm/V.sub.100 nm) is in the range 1 to 5.

The present invention relates to a hydrocarbon adsorbent with metal-impregnated zeolite particles having regular mesopores and a manufacturing method therefor. The hydrocarbon adsorbent includes a metal cation and a metal oxide that are impregnated in zeolite particles, in particular, the zeolite particles include regularly formed mesopores having a size of 2 to 10. By adjusting a Si/Al ratio and mesoporosity of the mesopores, a hydrocarbon adsorbent may have increased adsorption capacity for hydrocarbons in a cold-start section and can rapidly oxidize the hydrocarbon upon desorption thereof, thereby reducing the discharge of exhaust gas produced in automobiles and industries.

A hydrophobic adsorbent composition and process for removal of mercury from a gas phase fluid near the water and/or hydrocarbon dew point is disclosed herein.