A composite sorbent composition comprising a polymeric adsorbent; and an extractant having the formula (I), or hydrate in thereof, wherein X is O or S, A1 and A2 are each independently —C(O)— or —C(R′)(R″)— wherein R′, and R″ are each independently hydrogen, halogen, hydroxyl, cyano, nitro, amino, —CHO, —COOH, C1-12 alkyl, C1-4 alkoxy, C1-4 alkylamino, C1-2 haloalkyl, C1-2 haloalkoxy, C1-12 cycloalkyl, C6-12 aryl, C7-13 arylalkyl, C3-12 heteroaryl, C1-12 heteroalkyl, or C4-12 heteroarylalkyl, Z is a covalent bond, —S—, —O—, —SO2—, —SO—, —P(R)(═O)—, —NR—, -C(O)-, -C(O)NH-, —C(═N—R)—, or —C(R′)(R″)— wherein R, R′, and R″ are each independently hydrogen, halogen, hydroxyl, cyano, nitro, amino, —CHO, —COOH, —C(O)NH2, C1-12 alkyl, C1-12 alkoxy, C1-12 alkylamino, C1-4 haloalkyl, C1-4 haloalkoxy, C4-12 cycloalkyl, C6-12 aryl, C7-13 arylalkyl, C3-12 heterocycloalkyl, C3-12 heteroaryl, C1-12 heteroalkyl, or C4-12 heteroarylalkyl, and R1 and R2 are each independently hydrogen, halogen, hydroxyl, cyano, nitro, amino, or a substituted or unsubstituted monovalent C1-40 hydrocarbon.

##STR00001##

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).

The invention is a renewable adsorbent material, amine-functionalized chitin (AFC) that can remove the following munitions compounds from solution while providing a concentration-dependent color change: NTO, DNAN, and TNT. Adsorption of the munitions constituents can be adjusted by pH; neutral pH provides maximum adsorption. NTO can desorb from the AFC at pH levels of 2 and 12; DNAN and TNT remain attached to AFC once adsorbed.

Solid absorbent compositions and methods for the removal of mercaptan sulfur compounds from hydrocarbon streams are provided. The compositions may include porous granulated activated carbon particles with internal pore surfaces containing bound trinuclear basic iron (III) acetate complex containing the [Fe.sub.3(.sup.3-O)] core structure.

A method for producing a nanocomposite sorbent comprising carbon nanotube-grafted acrylic acid/acrylamide copolymer which involves copolymerization of acrylic acid and acrylamide in the presence of an aqueous dispersion of carbon nanotubes. The method yields a nanocomposite sorbent material having a reversible adsorption capacity phenol of 5 to 2500 g of phenol per mg of nanocomposite sorbent. Also disclosed is a method for removing organic pollutants from water using the nanocomposite sorbent.

Provided is a carbon dioxide absorbent including an ionic liquid including an imidazole-based anion and an aliphatic alcohol. Since an alcohol solvent included in the carbon dioxide absorbent according to one embodiment has low toxicity and a very high boiling point, the carbon dioxide absorbent has no problem of release into the atmosphere and consequent environmental pollution, and is chemically stable to significantly lower the possibility of release of decomposition products into the atmosphere. In addition, the carbon dioxide absorbent is also effective, since it may absorb carbon dioxide with a higher equivalent than an absorbent input equivalent, and has low regeneration energy so that carbon dioxide is easily desorbed.

A nucleophilic substitution reaction to crosslink cyclodextrin (CD) polymer with rigid aromatic groups, providing a high surface area, mesoporous CD-containing polymers (P-CDPs). The P-CDPs can be used for removing organic contaminants from water. By encapsulating pollutants to form well-defined host-guest complexes with complementary selectivities to activated carbon (AC) sorbents. The P-CDPs can rapidly sequester pharmaceuticals, pesticides, and other organic micropollutants, achieving equilibrium binding capacity in seconds with adsorption rate constants 15-200 times greater than ACs and nonporous CD sorbents. The CD polymer can be regenerated several times, through a room temperature washing procedure, with no loss in performance.

Provided herein are metal organic frameworks comprising metal nodes and N-donor organic ligands which have high selectivity and stability in the present of gases and vapors including H.sub.2S, H.sub.2O, and CO.sub.2. Methods include capturing one or more of H.sub.2S, H.sub.2O, and CO.sub.2 from fluid compositions, such as natural gas.

An example article includes a substrate and a coating applied to the substrate. The coating includes a stabilizer and an organic phosphonic acid reactant. In an example article, the coating includes a water-soluble polymer and an organic phosphate or phosphonate reactant. An example coating configured to be applied to a basic gas filter substrate includes a water-soluble polymer and an organic phosphate or phosphonate reactant. An example technique includes applying a coating to a substrate and heating at least the coating to a temperature between about 100 C. and about 275 C. for about 1 minute to about 10 minutes. An example system includes a basic gas filter including a coating, and a sensor configured to sense an optical change in the coating.

The purpose of the present disclosure is to provide a method for regenerating a highly water-absorbing polymer that has been deactivated by an acid, the method enabling formation of a highly water-absorbing recycled polymer having predetermined water absorption properties. The regeneration method according to the present disclosure is configured as follows. This method regenerates a highly water-absorbing polymer that has been deactivated by an acid into a highly water-absorbing recycled polymer having predetermined water absorption properties. The method includes: a preparation step (S1) for preparing a highly water-absorbing polymer which has an acid group and which has been deactivated by an acid; a highly water-absorbing recycled polymer-forming step (S3) for adding an alkali metal ion source, which can supply an alkali metal ion, to a regeneration-use aqueous solution that contains the highly water-absorbing polymer that has been deactivated by an acid, and forming the highly water-absorbing recycled polymer in a wet state from the highly water-absorbing polymer that has been deactivated by the acid; and a drying step for drying the highly water-absorbing recycled polymer in a wet state and forming the highly water-absorbing recycled polymer having the predetermined water absorption properties.