The present invention provides an integrated system of moisture removal, air purification, and air ventilation of the process air while some of the energy and resources required for operation of the system are self-sustained, or in some aspects the present system is self-regenerated such as heating and cooling of air and water exchanged among various elements/modules/members within the system or between the system and the surroundings, such that it becomes an all-time and all-round air dehumidifier, purifier and ventilator. Related method for removing air moisture from the surroundings using the present system is also provided.

The disclosure generally relates to CCS sorbents, particularly for CO.sub.2/H.sub.2O displacement desorption process. The sorbents include an aluminum oxide support that includes two alkali metal salts impregnated on the support. The two alkali metals include a potassium metal salts and a second alkali metal salt which is not potassium. The second metal salt disrupts poisoning effects that degrade sorbent lifetime. The sorbents demonstrate improved CO.sub.2 loadings and better H.sub.2O/CO.sub.2 ratios, as well as improved stability. Compositions and methods of making are disclosed.

This invention relates to modified MOF materials, methods of preparing them and processes using them. A modified MOF of the invention is modified by impregnating a MOF with an inorganic metal salt. The starting MOF contains at least one linker or ligand which contains an aryl amino group as part of its structure. These modified MOFs are able to adsorb either basic or acidic toxic industrial compounds (TIC). The modified MOFs can be used to remove TICs from various gaseous streams such as air.

Primary, secondary (1°,2°) alkylethylenediamine- and alkylpropylenediamine-appended variants of metal-organic framework are provided for CO.sub.2 capture applications. Increasing the size of the alkyl group on the secondary amine enhances the stability to diamine volatilization from the metal sites. Two-step adsorption/desorption profiles are overcome by minimzing steric interactions between adjacent ammonium carbamate chains. For instance, the isoreticularly expanded framework Mg.sub.2(dotpdc) (dotpdc.sup.4−=4,4″-dioxido-[1,1′:4′,1″-terphenyl]-3,3″-dicarboxylate), yields diamine-appended adsorbents displaying a single CO.sub.2 adsorption step. Further, use of the isomeric framework Mg-IRMOF-74-II or Mg.sub.2(pc-dobpdc) (pc-dobpdc.sup.4−=3,3-dioxidobiphenyl-4,4-dicarboxylate, pc=para-carboxylate) also leads to a single CO.sub.2 adsorption step with bulky diamines. By relieving steric interactions between adjacent ammonium carbamate chains, these frameworks enable step-shaped CO.sub.2 adsorption, decreased water co-adsorption, and increased stability to diamine loss. Variants of Mg.sub.2(dotpdc) and Mg.sub.2(pc-dobpdc) functionalized with large diamines such as N-(n-heptyl)ethylenediamine have utility as adsorbents for carbon capture applications.

A hydrocarbon removal system according an embodiment of the present invention includes: a first area including a first hydrocarbon adsorption catalyst having a first pore size; and a second area including a second hydrocarbon adsorption catalyst having a second pore size, wherein the first pore size may be smaller than the second pore size, the first hydrocarbon adsorption catalyst may include CHA zeolite, and the second hydrocarbon adsorption catalyst may include ZSM-5 zeolite.

A method for enhancing a sorbent membrane for carbon dioxide capture is disclosed. The method includes applying a layer of a hydrophobic material to at least one surface of the sorbent membrane. The hydrophobic material may be one of a polysioxane, a silicone compound, and a fluoroacrylic copolymer. The sorbent membrane may be an anionic exchange membrane, and may have a quaternary ammonium functional group. The layer of hydrophobic material reduces the amount of water used in the carbon dioxide capture process, and relaxes the water quality constraints.

Filter media comprising adsorptive particles are generally described. In some embodiments, the adsorptive particles are present in a relatively large amount, in a layer discrete from one or more other layers and/or fiber webs also present in the filter media, and/or in a layer that comprises a relatively low amount of fibers. In some embodiments, the filter media further comprises a non-woven fiber web comprising fibers with relatively small diameters.

A gas separation process in which the thermal storage of the heat in the gas is desired as well as the gas separation. This invention outlines a novel process and system whereby the thermal storage efficiency can be vastly increased by matching the gas sorption fronts and the thermal fronts to cause thermal front sharpening. The gas separation process and system include an adsorption vessel having an adsorbent in an amount of 10-40% and a thermal storage component in an amount of 50-90% by volume.

The invention relates to a method for cleaning corrosive process gases that contain sulfur compounds. According to the method, a gas stream that contains corrosive gases is conducted, in a sorption phase, over an inorganic sorbent material which absorbs at least one of the sorbable sulfurous components on the sorbent material, and the sulfurous compound-depleted gas stream is removed.

An apparatus and process for separating and removing CO.sub.2 generated by one or more passengers in the air in the interior of a cabin of a vehicle. Provided are: —a first stream of the air from the interior of the cabin to an interior of a container holding a loose particulate sorbent for CO.sub.2; —a second stream of air depleted in CO.sub.2 from the interior of the container holding the sorbent to an interior of the cabin; —a third stream of the air from exterior of the cabin to the inferior of the container holding the sorbent; and —a fourth stream of air enriched in CO.sub.2 from the interior of the container holding the sorbent to an exterior of the cabin.