To reduce loss due to water evaporation and to efficiently release moisture from a moisture absorbing portion, in the humidity controller according to the present invention, a moisture absorbing portion (2) is formed to include at least two gel sections each with a different thermal conductivity and to release absorbed moisture from an exposed surface (31) that is a specific region exposed outside and that is disposed on the surface opposite to a heater (5) on the basis of heating by the heater (5).

Disclosed are embodiments of a filter unit containing a water adsorbent material in the form of water adsorbent particles in a packed bed and a gas adsorbent material in the form of gas adsorbent particles in a packed bed. In embodiments, the gas adsorbent material is downstream from the water adsorbent material in a direction of operation. Further disclosed are methods of preparing and using the filter units.

A method of removing hydrogen interstitially dissolved within an object can include: positioning a sorption pad having a contact surface and comprising a sorptive material; urging the contact surface into metallurgical contact with the first target surface while at a treatment temperature that is greater than about 200 degrees Celsius; c) maintaining the metallurgical contact for a treatment period during which the hydrogen migrates from the target object to the sorptive material; and at the conclusion of the treatment period, separating the contact surface from the first target surface and moving the sorption pad and any hydrogen sequestered therein away from the object.

Disclosed are MOFs containing nucleophilic transition metal hydroxide (M-OH) groups. In certain embodiments, these MOFs can include a plurality of metal ions, each coordinated with one or more hydroxide ligands and one or more backbone ligands. In certain embodiments, the MOFs can comprise Kuratowski cluster-based secondary building units (SBUs). These MOFs can exhibit excellent performance for low pressure CO.sub.2 capture via a CO.sub.2/HCO.sub.3.sup.− fixation mechanism in which cooperative inter-cluster hydrogen bonding interactions enhance CO.sub.2 capture performance. Also provided are methods of making MOFs including one or more metal hydroxide moieties, as well as methods of using these MOFs to capture an acidic gas (e.g., CO.sub.2, SO.sub.2, NO.sub.2, or acetylene).

A carbon dioxide containing fluid is flowed through a membrane in an open position. The membrane encapsulates an adsorbent bed operating at a first temperature. The adsorbent bed adsorbs at least a portion of the carbon dioxide of the carbon dioxide containing fluid. The membrane is adjusted to a closed position, thereby isolating the adsorbent bed and preventing fluid flow into and out of the membrane. The adsorbent bed is heated to a second temperature, thereby desorbing the carbon dioxide captured from the carbon dioxide containing fluid. The membrane is adjusted to the open position. The adsorbent bed is cooled to the first temperature.

Systems and methods for an atmospheric carbon dioxide removal system that includes a plurality of carbon capture containers, a plurality of fans, an air diverter, and a velocity stack. Each of the carbon capture containers has an outwardly facing side and an inwardly facing side with the inwardly facing side facing an enclosed space. The fans are disposed adjacent to the carbon capture containers. The fans are arranged to move air through the carbon capture containers in a first direction from the outwardly facing side into the enclosed space. The air diverter is disposed within the enclosed space and receives the air flowing in the first direction and redirects the air to flow in a second direction that is angled upwardly from the first direction. The velocity stack is disposed on top of the enclosed space and is configured to accelerate the flow of the air in the second direction.

The disclosure relates to systems and methods for generating a brine solution using a salt bag for recharging zirconium phosphate in a reusable sorbent module. The salt bag can be a double layer bag. An inner water permeable bag can contain solid salts and can be surrounded by an outer water impermeable bag. Water can be added to dissolve the salts in the inner bag and the resulting solution can be collected as a brine solution for use in recharging the zirconium phosphate.

Methods of recovering iodine (I.sub.2) from a stream including iodine (I.sub.2) vapor and at least one of: an inert gas and water vapor can include contacting the stream with an alkaline solution to form an iodide salt, contacting the stream with an adsorbent to selectively adsorb water from the stream, contacting the stream with a concentrated acid to absorb the water vapor from the stream, desublimating or condensing the iodine (I.sub.2) vapor to form solid or liquid iodine (I.sub.2), or contacting the stream with a material to condense or de-sublimate the iodine (I.sub.2) vapor from the stream as the material at least one of: absorbs latent heat through a phase change of the material and absorbs sensible heat.

A solar reactor useful in reaction processes, more particularly, useful in endothermic reaction processes, such as a catalyzed process or an adsorption-desorption process. The reactor comprises a reaction pathway defined by an exterior wall and an interior wall, the exterior wall comprising a solar radiation receiver capable of converting solar radiation into heat and transmitting the heat to the reaction pathway. The reaction pathway has disposed therein, in alternating fashion, a plurality of reactive elements comprised of a catalyst or a sorbent and a plurality of heat transfer elements.

A system optionally including a carbon oxide reactor. A method for carbon oxide reactor control, optionally including selecting carbon oxide reactor aspects based on a desired output composition, running a carbon oxide reactor under controlled process conditions to produce a desired output composition, and/or altering the process conditions to alter the output composition.