A carbon pyrolyzate material is disclosed, having utility as an adsorbent as well as for energy storage and other applications. The pyrolyzate material comprises microporous carbon derived from low cost naturally-occurring carbohydrate source material such as polysaccharides. In adsorbent applications, the carbon pyrolyzate may for example be produced in a particulate form or a monolithic form, having high density and high pore volume to maximize gas storage and delivery, with the pore size distribution of the carbon pyrolyzate adsorbent being tunable via activation conditions to optimize storage capacity and delivery for specific gases of interest.

The inventive subject matter disclosed herein includes multiple novel filter media made of activated rice husks, as well as filtration systems and methods for removing contaminants from an aqueous solution, such as wastewater produced as a byproduct of various industrial processes, including mining, oil and gas exploration and extraction, farming, manufacturing, and the like.

[Object] To provide an adsorbent, an adsorbent sheet, and a carbon/polymer composite for adsorbing a virus having further improved virus adsorption capability. [Solving Means] An adsorbent for adsorbing a virus according to the present invention has a specific surface area value as measured by the nitrogen BET method of 10 m.sup.2/g or more and a pore volume as measured by the BJH method of 0.1 cm.sup.3/g or more. An adsorbent sheet for adsorbing a virus according to the present invention includes a porous carbonaceous material having a specific surface area value as measured by the nitrogen BET method of 10 m.sup.2/g or more and a pore volume as measured by the BJH method of 0.1 cm.sup.3/g or more. A carbon/polymer composite for adsorbing a virus according to the present invention includes a porous carbonaceous material having a specific surface area value as measured by the nitrogen BET method of 10 m.sup.2/g or more and a pore volume as measured by the BJH method of 0.1 cm.sup.3/g or more; and a binder.

A range of carbon materials can be produced using lignin in combination with synthetic phenolic resins or naturally occurring lingo-cellulosic materials. The lignin, which is essentially a naturally occurring phenolic resin, has a carbon yield on pyrolysis similar to that of the synthetic resins, which aids processing. The lignin can be used as a binder phase for synthetic resin or lignocellulosic materials allowing the production of monolithic carbons from a wide range of precursors, as the primary structural material where the thermal processing is modified by the addition of small quantities of synthetic resin materials or as structure modified in the production of meso/macro porous carbons in either bead, granular or monolithic form. A carbonised monolith is provided comprising mesoporous and/or macroporous carbon particles dispersed in a matrix of microporous carbon particles with voids between the particles defining paths for fluid to flow into and through the structure. The monolith may take the form of a shaped body having walls defining a multiplicity of internal transport channels for fluid flow, the transport channels being directed along the extrusion direction. The monolith may be made by carbonising a shaped phenolic body based on phenolic resin precursors. In a method for producing such a carbonisable shaped resin body solid particles of a first phenolic resin are provided which is partially cured so that the particles are sinterable but do not melt on carbonisation. The particles of the first phenolic resin are mixed with particles of a second phenolic resin that has a greater degree of cure than said first phenolic resin and has a mesoporous and/or macroporous microstructure that is preserved on carbonisation. The resulting mixture is formed into a dough e.g. by mixing the resin particles with methyl cellulose, PEO and water, after which the dough is extruded to form a shaped product and stabilising in its shape by sintering.

Filter material, mainly in form of industrial remnants from the production of the filter fillings, is processed without the intake of the heat in such a way that it is cut in the disintegrator (4) at the presence of the air, where the material is during retention time repeatedly led to the contact with the rotating blades and bunches emerge in the disintegrator (4) through aeration. The flat carrier (3) is thus at least partially disintegrated to the original fibers (1); the released fibers (1) intertwine into bunches and the active carbon (2) is released from the original bond with the flat carrier (3). The swirl (vortex) created inside the disintegrator (4) carries the dust particles of the active carbon (2) and they adhere to the surface of the fibers (1). Part of the released active carbon (2) isafter the separationcarried away from the emergin bunches, which in the lower part of the disintegrator (4) run through the sieve out of the disintegrator (4). The resulting product is advantageously applicable as heat and noise isolation in all fields of technology, for example construction. The separated active carbon (2) in form of granules is also a resulting product of processing.

The present invention provides a method (100) for removal of metals from aqueous solutions comprising the steps of treating (102) the aqueous solutions with an adsorbent, allowing (104) the aqueous solutions and the adsorbent to be in contact for a predetermined time to obtain treated aqueous solutions, collecting (106) the treated aqueous solutions, filtering (108) the treated aqueous solutions and discharging (110) the filtered aqueous solutions. The adsorbent comprising plurality of natural biomaterials. Further, the plurality of natural biomaterials are capable of adsorbing the metals from the aqueous solutions.

A functionalized asphaltene, obtained by refluxing with an acid solution. The functionalized asphaltene contains elevated levels of oxygen content due to nitration and oxidation of the refluxing process. The refluxing process also imparts organic functional groups including at least amines, nitro groups carbonyl groups, carboxylic groups and hydroxyl groups to the functionalized asphaltene, and these functional groups are attached to, thereby coating the surface of a functionalized asphaltene particle. A method for removing dye compounds from an aqueous sample with the functionalized asphaltene is also described.

A carbon pyrolyzate material is disclosed, having utility as an adsorbent as well as for energy storage and other applications. The pyrolyzate material comprises microporous carbon derived from low cost naturally-occurring carbohydrate source material such as polysaccharides. In adsorbent applications, the carbon pyrolyzate may for example be produced in a particulate form or a monolithic form, having high density and high pore volume to maximize gas storage and delivery, with the pore size distribution of the carbon pyrolyzate adsorbent being tunable via activation conditions to optimize storage capacity and delivery for specific gases of interest.

Provided is a purifying material capable of highly efficiently removing contaminant components from wastewater. A water purifying material having a composition of 30 to 40% total iron, 1 to 5% titanium, 0.1 to 1% magnesium, and 0.1 to 0.8% silica (silicon), and a method for manufacturing the water purifying material including: adding caustic soda to a solution containing 200 to 100 mg/L of bivalent iron, 20 to 100 mg/L of titanium ions, 5 to 50 mg/L of magnesium, and 3 to 30 mg/L of silica under conditions of 30 to 50 C. and pH 6.8 to 7.2 to carry out neutralization and reaction; separating and collecting an obtained solid at 100 C. or less; and drying the collected solid.

A functionalized asphaltene, obtained by refluxing with an acid solution. The functionalized asphaltene contains elevated levels of oxygen content due to nitration and oxidation of the refluxing process. The refluxing process also imparts organic functional groups including at least amines, nitro groups carbonyl groups, carboxylic groups and hydroxyl groups to the functionalized asphaltene, and these functional groups are attached to, thereby coating the surface of a functionalized asphaltene particle. A method for removing dye compounds from an aqueous sample with the functionalized asphaltene is also described.