A method of fabricating a magnetically-controlled graphene-based micro-/nano-motor includes: (a) mixing FeCl.sub.3 crystal powder with deionized water to obtain a FeCl.sub.3 solution; (b) completely immersing a carbon-based microsphere in the FeCl.sub.3 solution; transferring the carbon-based microsphere from the FeCl.sub.3 solution followed by heating to allow crystallization of FeCl.sub.3 on the surface of the carbon-based microsphere to obtain a FeCl.sub.3-carbon-based microsphere; (c) heating the FeCl.sub.3-carbon-based microsphere in a vacuum chamber until there is no moisture in the vacuum chamber; continuously removing gas in the vacuum chamber and introducing oxygen; and treating the FeCl.sub.3-carbon-based microsphere with a laser in an oxygen-enriched environment to obtain the magnetically controlled graphene-based micro-/nano-motor. A magnetically-controlled graphene-based micro-/nano-motor is further provided.

Provided is a high-loading and alkali-resistant protein A magnetic bead. The magnetic bead can maintain chemical stability under pH 2-14 and has an immunoglobulin G (IgG) binding capacity greater than 50 mg/mL. Further provided is a method for purifying and/or detecting an immunoglobulin, comprising a step of contacting a sample containing the immunoglobulin with the high-loading and alkali-resistant protein A magnetic bead. The alkali-resistant protein A magnetic bead can realize rapid purification of immunoglobulin, saving about 80% of treatment time and reducing total purification costs by 50%. In addition, the alkali-resistant protein A magnetic bead has high alkali resistance. An alkaline method for in situ cleaning can be performed to regenerate the magnetic bead after use. The magnetic bead has rapid magnetic response and good dispersiveness, realizing rapid magnetic bead enrichment, cleaning, and elution. The magnetic bead facilitates automated, high-throughput, and large volume purification of a sample.

The invention relates to a cyclic method of producing a hydrogen rich and/or a carbon monoxide rich stream using different materials, a first solid material, a second solid material and a CO.sub.2 sorbent material.

In a first step a first gas stream comprising steam and at least one reductant is brought in contact with the three materials resulting in a hydrogen rich outlet stream.

In a second step, the captured CO.sub.2 from the first step is released and converted to CO to produce a CO rich outlet stream.

The invention further relates to an installation for producing a hydrogen rich and/or carbon monoxide rich stream.

A cylindrical column-shaped honeycomb adsorbent has a plurality of cell passages extending along an axial direction of the honeycomb adsorbent. The plurality of cell passages are configured so that a pitch of adjacent cell passages is within a range of 1.5 mm˜1.8 mm, and so that a thickness of a wall between the cell passages is within a range of 0.45 mm˜0.60 mm. With this configuration, the honeycomb adsorbent exhibits BWC (Butane Working Capacity) of 6.5 g/dL or greater. By mixing fibrous meltable core melting away during baking, the honeycomb adsorbent has macropores configured to have a volume of 0.15 mL/g˜0.35 mL/g with respect to an overall weight of the honeycomb adsorbent and metal oxide particles having a proportion of weight of 150˜250% with respect to the activated carbon.

The invention relates to a cyclic method for capturing and utilizing CO.sub.2 contained in a gas stream. The method uses three different materials, a first solid material, a second solid material and a CO.sub.2 sorbent material.

In a first step a first gas stream comprising CO.sub.2 and at least one reductant is brought in contact with the three materials, resulting in an outlet stream comprising water. In a second step, the captured CO.sub.2 from the first step is released and converted to CO to produce a CO rich outlet stream. The invention further relates to an installation for capturing and utilizing CO.sub.2.

A filter for a liquid purifier, comprising: a filter housing having an inlet to receive water and an outlet to discharge the water; and a filter module provided in the filter housing, and configured to purify water introduced through the inlet, and to provide the purified water to the outlet, wherein the filter module includes a carbon block having a hollow tube shape by mixing activated carbon, a binder, ferric hydroxide, and titanium oxide, and the binder is mixed at a ratio of 13% to 23% by weight.

Disclosed are a functional material for synchronously stabilizing multiple metals and a preparation method thereof, and a method for rehabilitating soil or wastewater contaminated by heavy metals (metalloids). The preparation method includes: mixing a ferrous salt, a ferric salt, a manganous salt, water, a dispersing material, and a phosphate to obtain a first mixture, and subjecting the first mixture to a first precipitation reaction to obtain a first reaction mixture containing the phosphate; adjusting a pH value of the first reaction mixture containing the phosphate to 10-12 by adding an alkali thereto to obtain a second mixture, subjecting the second mixture to a second precipitation reaction to obtain a second reaction mixture; and subjecting the second reaction mixture to a solid-liquid separation to obtain a solid, washing the solid, and drying to obtain the functional material for synchronously stabilizing multiple metals.

A porous carbon material composite formed of a porous carbon material and a functional material and equipped with high functionality. The porous carbon material composite is formed of (A) a porous carbon material obtainable from a plant-derived material having a silicon (Si) content of 5 wt % or higher as a raw material; and (B) a functional material adhered on the porous carbon material, and has a specific surface area of 10 m.sup.2/g or greater as determined by the nitrogen BET method and a pore volume of 0.1 cm.sup.3/g or greater as determined by the BJH method and MP method.

A first process and sorbent for removing ammonia from a gaseous environment, the sorbent comprised of graphene oxide having supported thereon at least one compound selected from metal salts, metal oxides and acids, each of which is capable of adsorbing ammonia. A second process and sorbent system for removing ammonia and a volatile organic compound from a gaseous environment; the sorbent system comprised of two graphene-based materials: (a) the aforementioned graphene oxide, and (b) a nitrogen and oxygen-functionalized graphene. The sorbents are regenerable under a pressure gradient with little or no application of heat. The processes are operable through multiple adsorption-desorption cycles and are applicable to purifying and revitalizing air contaminated with ammonia and organic compounds as may be found in spacesuits, aerospace cabins, underwater vehicles, and other confined-entry environments.

Functionalized particulate support material and chromatographic media prepared therefrom are disclosed. The functionalized particulate support material is a plurality of particles, each particle having a particle surface. Chemically bonded to and extending from the surface of the particles is a combination of hydrophobic and hydrophilic functional groups. The hydrophobic functional groups enable polymerization of one or more monomers onto the particle surface while the hydrophilic functional groups provide increased wettability of the particle surface compared to an unmodified particle surface. The functionalized particulate support material may be further processed so as to form polymer chains extending from the hydrophobic functional groups. In one embodiment, the resulting polymer functionalized material is useful as a chromatographic media in chromatography columns or cartridges, such as in a liquid chromatography (HPLC) column. Chromatography columns or cartridges containing the polymer functionalized media, and methods of making and using the media, are also disclosed.