Amine functional solid sorbents for carbon dioxide capture and sequestration may be prepared from metal oxide foam solid sorbent supports by treating an appropriate metal oxide foam solid sorbent support with an amine material. Desirable are metal oxide foam solid sorbent supports with a foam structure and morphology at least substantially absent hollow sphere, layered sphere, wormlike and amorphous structure and morphology components. The amine materials may be sorbed into the metal oxide foam solid sorbent support, or alternatively chemically bonded, such as but not limited to covalently bonded, to the metal oxide foam solid sorbent support.

A support for a polymer electrolyte fuel cell catalyst satisfying the following requirements (A), (B), (C), and (D), and a producing method thereof, as well as a catalyst layer for a polymer electrolyte fuel cell and a fuel cell:

(A) a specific surface area according to a BET analysis of a nitrogen adsorption isotherm is from 450 to 1500 m.sup.2/g.
(B) a nitrogen adsorption and desorption isotherm forms a hysteresis loop in a range of relative pressure P/P.sub.0 of more than 0.47 but not more than 0.90, and a hysteresis loop area S.sub.0.47-0.9 is from 1 to 35 mL/g;
(C) a relative pressure P.sub.close/P.sub.0 at which the hysteresis loop closes is more than 0.47 but not more than 0.70; and
(D) a half-width of a G band detected by Raman spectrometry in a range of from 1500 to 1700 cm.sup.1 is from 45 to 75 cm.sup.1.

A solid phase microextraction substrate is disclosed. The solid phase microextraction substrate has a sorbent coating on at least part of a surface thereof. The coating is adapted for extracting at least one analyte component from a fluid matrix. The coating includes sorbent particles in a polymeric adhesive matrix. A majority of pores in each sorbent particle in the coating do not contain substantially any of the polymeric adhesive matrices.

Provided are a composition and a manufacturing method of a solid CO.sub.2 sorbent having excellent physical properties and chemical reaction characteristics, particularly having an excellent mid-temperature range activity for a fluidized bed process, for use in collecting a CO.sub.2 source (pre-combustion or pre-utilization) in syngas application fields such as integrated coal gasification combined cycle (IGCC) power systems, synthetic natural gas (SNG) and synthetic liquid fuel (CTL).

Oxalic acid is employed in a precursor mixture containing at least one milled alpha alumina powder having a particle size of 0.1 to 6 microns, boehmite powder that functions as a binder of the alpha alumina powders, and at least one burnout material having a particle size of 1-10 microns to provide a porous body having enhanced pore architecture in which extrusion cracks can be reduced. The presence of oxalic acid in such as precursor mixture can reduce and even eliminate NOx emission during a high temperature heat treatment process.

Described herein is a technology for the creation of smooth metal oxide films or coatings using organic cross-linking agents to enable low-temperature sintering. These metal oxide films can be used in conjunction with low-melting temperature substrates, such as plastics, metal, metal oxide, and glass, providing exquisite control over surface roughness.

The present invention relates to a zeolite adsorbent having an external surface area of between 20 m.sup.2.Math.g.sup.1 and 70 m.sup.2.Math.g.sup.1, a mesopore volume (V.sub.meso) of less than or equal to 0.20 cm.sup.3.Math.g.sup.1, and a content of non-zeolite phase (NZP) of less than or equal to 6%, and in which at least one of its dimensions is greater than or equal to 30 m. The invention also relates to the process for preparing said zeolite materials in agglomerated form and to the uses thereof for gas-phase or liquid-phase separation operations.

A method for making an adsorbent composite can include activating dried lemon peel pieces to obtain activated lemon peel pieces; pyrolyzing the activated lemon peel pieces to obtain activated lemon peel char; dissolving at least one polymer in an organic solvent to obtain a polymer solution; dispersing the activated lemon peel char in the polymer solution to obtain a mixture; extracting the organic solvent from the mixture to obtain a composite; and annealing the composite to provide the adsorbent composite.

A substrate includes a double-network polymer system including a cross-linked, covalently-bonded polymer and a reversible, partially ionicly-bonded polymer, wherein the substrate has a moisture level less than or equal to 15 percent of the total weight of the substrate, wherein the substrate is porous, and wherein the substrate includes a latent retractive force. A method for manufacturing a substrate includes producing a double-network hydrogel including a cross-linked, covalently-bonded polymer and a reversible, ionicly-bonded polymer; elongating by force the double-network hydrogel in at least one direction; treating the double-network hydrogel with an organic solvent with a volatile and water-miscible organic solvent to replace a majority of water within the double-network hydrogel; evaporating the organic solvent while the double-network hydrogel is still elongated to form a substantially-dried double-network polymer system; and releasing the force to produce the substrate.

A substrate includes a double-network polymer system including a cross-linked, covalently-bonded polymer and a reversible, partially ionicly-bonded polymer, wherein the substrate has a moisture level less than or equal to 15 percent of the total weight of the substrate, wherein the substrate is porous, and wherein the substrate includes a latent retractive force. A method for manufacturing a substrate includes producing a double-network hydrogel including a cross-linked, covalently-bonded polymer and a reversible, ionicly-bonded polymer; elongating by force the double-network hydrogel in at least one direction; treating the double-network hydrogel with an organic solvent with a volatile and water-miscible organic solvent to replace a majority of water within the double-network hydrogel; evaporating the organic solvent while the double-network hydrogel is still elongated to form a substantially-dried double-network polymer system; and releasing the force to produce the substrate.