A product for adsorbing one or more heavy metals from a liquid is disclosed. The product may comprise attapulgite that has been surface functionalized with a surface coating agent that includes one or more mercury affinity functional groups that chemically bond to the attapulgite surface, wherein the weight percentage of components of the product includes: 91-99 wt. % attapulgite and 1-9 wt. % surface coating agent that includes the one or more mercury affinity functional groups. The product has a surface area in the range of 115-145 m.sup.2/g as measured using the BET method. The heavy metal includes mercury and/or lead. Also disclosed is a method of producing the product and a method of adsorbing at least one heavy metal in a liquid using the product.

The present invention relates to the CO.sub.2 and O.sub.2 remover. The CO.sub.2 and O.sub.2 remover comprises 65 to 85 weight percent (wt. %) of a nickel oxide (NiO), 5 to 20 wt. % of a magnesium oxide (MgO), wherein the weight ratio of the nickel oxide and the magnesium oxide (NiO/MgO) is 4 to 11, and wherein the wt. % is based on the weight of the CO.sub.2 and O.sub.2 remover.

A process is disclosed for the removal of hydrogen sulfide (H.sub.2S) from natural. This process provides for passing a natural gas feedstream comprising H.sub.2S though a regenerable adsorbent media which adsorbs H.sub.2S to provide an H.sub.2S-lean natural gas product and H.sub.2S. The regenerable adsorbent media of the present invention is a tertiary amine functionalized cross-linked macroporous polymeric adsorbent media.

The present invention concerns the use, for gas separation, of at least one zeolite adsorbent material comprising at least one FAU zeolite, said adsorbent having an external surface area greater than 20 m.sup.2.Math.g.sup.−1, a non-zeolite phase (PNZ) content such that 0<PNZ≦30%, and an Si/Al atomic ratio of between 1 and 2.5. The invention also concerns a zeolite adsorbent material having an Si/Al ratio such that 1≦Si/Al<2.5, a mesoporous volume of between 0.08 cm.sup.3.Math.g.sup.−1 and 0.25 cm.sup.3.Math.g.sup.−1, a (Vmicro−Vmeso)/Vmicro ratio of between −0.5 and 1.0, non-inclusive, and a non-zeolite phase (PNZ) content such that 0<PNZ≦30%.

In some embodiments, the present disclosure pertains to methods of capturing CO.sub.2 from an environment by hydrating a porous material with water molecules to the extent thereby to define a preselected region of a plurality of hydrated pores and yet to the extent to allow the preselected region of a plurality of pores of the porous material to uptake gas molecules; positioning the porous material within a CO.sub.2 associated environment; and capturing CO.sub.2 by the hydrated porous material. In some embodiments, the pore volume of the hydrated porous material includes between 90% and 20% of the pre-hydrated pore volume to provide unhydrated pore volume within the porous material for enhanced selective uptake of CO.sub.2 in the CO.sub.2 associated environment. In some embodiments, the step of capturing includes forming CO.sub.2-hydrates within the pores of the porous material, where the CO.sub.2.Math.n/H.sub.2O ratio is n<4.

Method for separating gaseous carbon dioxide from air, in particular from ambient atmospheric air (1), by cyclic adsorption/desorption using a sorbent material (3), wherein said sorbent material (3) is a solid inorganic or organic, non-polymeric or polymeric support material functionalized on the surface with amino functionalities capable of reversibly binding carbon dioxide, with a specific BET surface area, preferably measured by nitrogen adsorption, in the range of 1-20 m2/g.

The present invention relates, inter alia, to the use of porous crystalline solids constituted of a metal-organic framework (MOF) for the selective adsorption of aldehyde volatile organic compounds.

The MOF solids of the present invention can be used for the improved purification of dry or humid air, and for the manufacture of regenerable filters for air purification, particularly leak-free regenerable air filters.

The invention relates to an apparatus (1) for catalytic decomposition of nitrous oxide in a gas stream derived from exhalation air from a patient. The apparatus (1) comprises an inlet arrangement (2) with a gas inlet (3) for the exhalation air, an outlet arrangement (11) with a gas outlet (12) for an outlet gas, and between these arrangements a through-flow decomposition chamber (9) containing a catalyst material. According to the invention the apparatus is provided with a nitrous oxide adsorption/desorption means (4) in the inlet arrangement (2) for level out variations in the concentration of nitrous oxide fed to the decomposition chamber (9).

The invention refers to a method for manufacturing a catalytic device, with the steps: a) providing a first catalyst having photocatalytic activity, a second catalyst, which is a different molecule than the first catalyst, and an adsorbent, each in a powdered state, b) mingling the first catalyst, the second catalyst and the adsorbent to form a catalytic composition and suspending them in a suspension liquid to form a slurry, and c) repeatedly coating the slurry onto a solid grid-like carrier having a plurality of through holes, configured to allow a gas to flow through the carrier, and evaporating the suspension liquid.

Smoking article include a smokable material and an activated carbon particle downstream of the smokable material. The activated carbon particle is produced from a whole seed. The activated carbon particle has a length, width and height. At least two of the length width and height are independently in a range from about 1 mm to about 7.5 mm. The particles can be spheroids, in which case the length, width and height would be the same or similar.