A method of preparing a superabsorbent polymer, which enables the preparation of the superabsorbent polymer exhibiting an improved absorption rate while maintaining excellent absorption performances is provided. The method of preparing the superabsorbent polymer includes carrying out a crosslinking polymerization of a water-soluble ethylene-based unsaturated monomer having acidic groups which are at least partially neutralized, in the presence of an internal crosslinking agent having a predetermined chemical structure to form a water-containing gel polymer, gel-pulverizing the water-containing gel polymer, drying, pulverizing, and size-sorting the gel-pulverized water-containing gel polymer to form a base polymer powder, and carrying out a surface crosslinking of the base polymer powder by a heat treatment in the presence of a surface crosslinking agent, wherein the gel-pulverizing is carried out by extruding the water-containing gel polymer through a porous plate having a plurality of holes using a screw extruder mounted inside a cylindrical pulverizer under a condition that a chopping index is 28 (/s) or more.

The present disclosure provides for a porous gas sorbent monolith with superior gravimetric working capacity and volumetric capacity, a gas storage system including a porous gas sorbent monolith of the present disclosure, methods of making the same, and method for storing a gas. The porous gas sorbent monolith includes a gas adsorbing material and a non-aqueous binder.

A preparation method of a granular adsorbent is provided, including the following: adding a pyrrole monomer to an acidic solution, and adding an oxidant as an initiator to allow a polymerization reaction of the pyrrole monomer to produce polypyrrole (PPy), where an adsorption material powder is added to a reaction system before, during, or immediately after the polymerization reaction, and a resulting mixture is thoroughly stirred; after the polymerization reaction is completed, filtering a resulting reaction system to obtain a filter cake, which is the granular adsorbent; or subjecting the resulting reaction system to centrifugal sedimentation to obtain the monolithic adsorbent. In the present disclosure, the pyrrole monomer is subjected to a polymerization reaction to generate PPy; before being tightly stacked, network structures of PPy wrap the adsorption material powder; and the granular adsorbent is formed through sedimentation and stacking.

The present invention relates to a molding comprising a zeolitic material having framework type MWW, wherein the framework structure comprises Ti, Si, and O, wherein the zeolitic material further comprises Zn and an alkaline earth metal M, the molding further comprising a binder, wherein the molding exhibits a specific Lewis acidity. Further, the present invention relates to the method of preparation of said molding and the use thereof.

The present invention relates to a calcined medium, in particular a catalyst or a catalyst medium or an adsorbent/absorbent mass, in particular in the form of extrudates, pellets, granules or beads, the medium comprising a porous matrix comprising carbonates, clays, zeolites, oxides, or metal and/or silicon hydroxides, and the matrix incorporating hollow mineral microspheres having a different composition in a content of between 0.3 and 50% by weight, in particular between 0.5 and 15% by weight, of the matrix.

Methods for forming a carbon molecular sieve includes loading polymer fibers into a mold and heating the mold containing the polymer fibers to a temperature in a range from 50 ° C. to 350 ° C. to form a polymer monolith. The polymer monolith is then pyrolized by heating to a temperature in a range from 500 ° C. to 1700 ° C. A carbon molecular sieve monolith includes a first end and a second end opposite the first end, and carbon molecular sieve fibers aligned in parallel from the first end of the carbon molecular sieve monolith to the second end of the carbon molecular sieve monolith. Channels extend from the first end of the carbon molecular sieve monolith to the second end of the carbon molecular sieve monolith, and outer surfaces of the carbon molecular sieve fibers are joined. The carbon molecular sieve monolith has a cell density of greater than 500 cells per square inch.

The present invention relates to novel sulfur-doped carbonaceous porous materials. The present invention also relates to processes for the preparation of these materials and to the use of these materials in applications such as gas adsorption, mercury and gold capture, gas storage and as catalysts or catalyst supports.

The invention relates to a method to produce a particulate activated carbon material for capturing CO.sub.2 from air, wherein the particulate activated carbon is impregnated with alkali carbonate salt such as K.sub.2CO.sub.3; and wherein the impregnated particulate activated carbon either has, determined using nitrogen adsorption methods, a pore volume of at least 0.10 cm.sup.3/g for pore sizes of at least 5 nm and a pore volume of at most 0.30 cm.sup.3/g for pore sizes of less than 2 nm or is based on a mixture of different alkali carbonate salts, or has a particular pore surface for pore sizes in the range of 2 nm-50 nm.

This disclosure provides a method of making a high-fixed-carbon material comprising pyrolyzing biomass to generate intermediate solids and a pyrolysis vapor; condensing the pyrolysis vapor to generate pyrolysis liquid; blending the pyrolysis liquid with the intermediate solids, to generate a mixture; and further pyrolyzing the mixture to generate a high-fixed-carbon material. A process can comprise: pyrolyzing a biomass-comprising feedstock in a first pyrolysis reactor to generate a first biogenic reagent and a first pyrolysis vapor; introducing the first pyrolysis vapor to a condensing system to generate a condenser liquid; contacting the first biogenic reagent with the condenser liquid, thereby generating an intermediate material; further pyrolyzing the intermediate material in a second pyrolysis reactor to generate a second biogenic reagent and a second pyrolysis vapor; and recovering the second biogenic reagent as a high-yield biocarbon composition. The process can further comprise pelletizing the intermediate material. Many process and system configurations are disclosed.

The present invention relates to a neutralizing absorbent for decontaminating a leaked chemical substance, a method of preparing the same, and a neutralizer filled with the same. The neutralizing absorbent for decontaminating a leaked chemical substance according to the present invention includes an inorganic adsorbent, which is commonly usable in neutralizing absorption of acidic, basic, and/or organic chemical substances, at 40 to 60 wt %, a thickener at 20 to 30 wt %, a surfactant at 20 to 30 wt %, and a color change indicator, and is formulated in a solid state. The neutralizing absorbent is effective in promptly and safely taking an initial action regardless of the type, nature, and characteristics of acidic, basic, and/or organic chemical substances leaked in the leakage accident of the chemical substance, and accordingly, is useful in preventing secondary accidents. Also, when the neutralizing absorbent is used, there are no concerns about the spread of contamination due to water generated by an acid-base reaction, concerns about the additional occurrence of secondary contamination due to a decontaminating agent can be minimized by using a non-toxic chemical absorbent, and a decontamination process can be visually checked in real time regardless of the type, nature, and characteristics of the leaked chemical substance. Furthermore, when a neutralizer filled with the neutralizing absorbent for decontaminating a leaked chemical substance according to the present invention is used, the leaked chemical substance can be more safely and effectively decontaminated during an initial action.