A method for enhancing sorption performance of a sorbent material includes the step of increasing a surface area of the sorbent material for adsorption of a fluid at an interface between the fluid and the sorbent material by arranging one or more apertures to be disposed on the sorbent material, wherein each of the one or more apertures is further arranged to define an interior space for absorption of the fluid.

A soil improver for increasing the liquid storage capacity of soils made of a plastic foam, the plastic foam having at least predominantly open cells, characterized in that the plastic foam has a raw density of 5 to 15 kg/m.sup.3. The invention also relates to a method for producing a plastic foam of such a soil improver.

The disclosure pertains to a microstructure for adsorbing/desorbing at least one gas component of a gas supplied to the microstructure. The microstructure includes a semiconductor substrate having a bottom and a top. The microstructure also includes a plurality of micro-channels, extending from the bottom to the top of the semiconductor substrate. A top surface of micro-channel is configured to adsorb and/or desorb the at least one gas component when the gas is passed through the micro-channels.

The present disclosure provides advantageous graphene/graphite stabilized composites (e.g., graphene/graphite stabilized emulsion-templated foam composites), and improved methods for fabricating such graphene/graphite stabilized composites. More particularly, the present disclosure provides improved methods for fabricating pristine, graphene/graphite/polymer composite foams derived from emulsions stabilized by graphene/graphite kinetic trapping. In exemplary embodiments, the present disclosure provides that, instead of viewing the insolubility of pristine graphene/graphite as an obstacle to be overcome, it is utilized as a means to create or fabricate water/oil emulsions, with graphene/graphite stabilizing the spheres formed. These emulsions are then the frameworks used to make foam composites that have shown bulk conductivities up to about 2 S/m, as well as compressive moduli up to about 100 MPa and breaking strengths of over 1200 psi, with densities as low as about 0.25 g/cm.sup.3.

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.

The present disclosure provides advantageous graphene/graphite stabilized composites (e.g., graphene/graphite stabilized emulsion-templated foam composites), and improved methods for fabricating such graphene/graphite stabilized composites. More particularly, the present disclosure provides improved methods for fabricating pristine, graphene/graphite/polymer composite foams derived from emulsions stabilized by graphene/graphite kinetic trapping. In exemplary embodiments, the present disclosure provides that, instead of viewing the insolubility of pristine graphene/graphite as an obstacle to be overcome, it is utilized as a means to create or fabricate water/oil emulsions, with graphene/graphite stabilizing the spheres formed. These emulsions are then the frameworks used to make foam composites that have shown bulk conductivities up to about 2 S/m, as well as compressive moduli up to about 100 MPa and breaking strengths of over 1200 psi, with densities as low as about 0.25 g/cm.sup.3.

The invention relates to a substantially laminary manufacture comprising 2 substantially laminary layers in contact, wherein the layers comprise a woven, hydrophilic material.

A process for the production of high-quality activated carbons from carbonized, self-regenerating, carbon-containing biomasses selects the carbonized biomasses from HTC carbon from fruit stones and HTC carbon from nut shells. The carbonized biomasses together with potassium hydroxide, sodium hydroxide or a mixture of both hydroxides as activator are subjected to a heat treatment at temperatures at which the activator exists in the form of a melt. The activator and the carbonized biomasses are present in a weight ratio of 0.5:1 to 6:1 at the beginning of the heat treatment.

A method of adsorption includes contacting a nanocomposite with a solution including one or more pollutants. The nanocomposite is a graphite-phase carbon nitride copper oxide and magnesium aluminum oxide (g-C.sub.3N.sub.4@CuO/MgAl.sub.2O.sub.4) material and includes a graphite-phase carbon nitride (g-C.sub.3N.sub.4) in an amount of 5 to 15 percent by weight (wt. %), copper oxide in an amount of 3 to 7 wt. %, and magnesium aluminum oxide (MgAl.sub.2O.sub.4) in an amount of 80 to 90 wt. % based on a total weight of the g-C.sub.3N.sub.4@CuO/MgAl.sub.2O.sub.4 material. The method further includes adsorbing the one or more pollutants on the nanocomposite.

Disclosed are methods of making a porous particle material for use as stationary media and related chromatographic separation devices utilizing the disclosed stationary media. The porous particle material has a pore volume that yields improved stability and column lifetime, and additionally has a modified surface, resulting in a surface modified porous particle material that improves the separation of AAVs from their aggregates in the samples to be tested.