Patent classifications
B01J20/30
LANTHANUM-IRON-LOADED CARBON NANOTUBE FILM FOR ENVIRONMENTAL RESTORATION, PREPARATION AND APPLICATION THEREOF
A preparation method of a lanthanum-iron-loaded carbon nanotube film for environmental restoration is provided, it belongs to the technical field of composite materials. The preparation method includes: mixing carbon nanotubes with a lanthanum-iron mixed solution to obtain a suspension, then obtaining a first reaction solution by a constant temperature oscillation reaction; adding alkali liquor into the first reaction solution to obtain a second reaction solution by an oscillation reaction; carrying out a solid-liquid separation on the second reaction solution, adding the obtained solid after drying into an organic solution, and obtaining a third reaction solution by ultrasonic mixing; centrifuging the third reaction solution to obtain a supernatant; obtaining a lanthanum-iron-loaded carbon nanotube film by suction filtration. Compared with powdered adsorbent and single adsorbent, the material prepared by the preparation method has advantages of strong stability, high adsorption efficiency, good regeneration effect, high recycling efficiency, and low production.
LIGNIN-BASED HIERARCHICAL POROUS CARBON WITH HIGH SPECIFIC SURFACE AREA AND PREPARATION METHOD AND APPLICATION THEREOF
The present invention discloses a lignin-based hierarchical porous carbon with high specific surface area and preparation method and application thereof. The present invention employs maleic anhydride, acrylic acid, and hypophosphorous acid to modify a lignin, then performs a cross-linking reaction with a glutaraldehyde-triethanolamine condensate to prepare a lignin graft-copolymerized by phosphino carboxylic acid copolymer, and then dropwise adding a soluble calcium salt solution and a soluble carbonate solution into the lignin graft-copolymerized by phosphino carboxylic acid copolymer dispersion successively, co-precipitates to prepare a lignin/nano CaCO.sub.3 complex, finally obtains a lignin-based hierarchical porous carbon with high specific surface area through carbonizing at a high temperature. The preparation method of the present invention may enable nano CaCO.sub.3 to be uniformly and stably dispersed in a three-dimensional network structure of the lignin graft-copolymerized by phosphino carboxylic acid copolymer, realizing full and uniform complexation of the lignin with nano CaCO.sub.3.
Adsorption method for at least one of cesium and strontium employing silicotitanate having sitinakite structure
The present invention provides a composition that includes a silicotitanate that has a sitinakite structure, the composition having higher cesium adsorptivity than conventional compositions. The present invention also provides a production method for the composition that includes a silicotitanate that has a sitinakite structure. The production method does not require the use of hazardous or deleterious materials, can generate a product using a compound that is easily acquired, and can use a general-purpose autoclave. Also provided is a silicotitanate composition that has higher strontium adsorptivity than the present invention. Provided is a silicotitanate composition that contains niobium and a silicotitanate that has a sitinakite structure, the composition having at least two or more diffraction peaks selected from the group consisting of 2θ=8.8°±0.5°, 2θ=10.0°±0.5°, and 2θ=29.6°±0.5°.
Advanced porous carbonaceous materials and methods to prepare them
The present invention concerns porous carbonaceous particles having pores including micropores and macropores, having a mean diameter, determined by laser diffraction, ranging from 15 to 100 μm and porous carbonaceous monoliths comprising aggregates of said carbonaceous particles.
Adsorption structure, adsorption structure unit, and method for manufacturing same
An adsorption structure unit prevents water leakage from an adsorption structure and improves the durability of the adsorption structure and the durability of the adsorption structure unit. An adsorption structure has a filter portion having a plurality of flow paths divided by a plurality of partition walls and a plugged portion shutting a feed water inflow or outflow end of the plurality of flow paths, a water-impermeable outer tube accommodating the filter portion, and a seal material blocking a gap between the filter portion and the outer tube in at least one end portion of the filter portion. An adsorption structure unit has the adsorption structure, a housing supplying feed water from one end of the adsorption structure, and discharging the feed water from the other end, and a ring member disposed between end portions on both sides of the outer tube and an inner surface of the housing.
Adsorption structure, adsorption structure unit, and method for manufacturing same
An adsorption structure unit prevents water leakage from an adsorption structure and improves the durability of the adsorption structure and the durability of the adsorption structure unit. An adsorption structure has a filter portion having a plurality of flow paths divided by a plurality of partition walls and a plugged portion shutting a feed water inflow or outflow end of the plurality of flow paths, a water-impermeable outer tube accommodating the filter portion, and a seal material blocking a gap between the filter portion and the outer tube in at least one end portion of the filter portion. An adsorption structure unit has the adsorption structure, a housing supplying feed water from one end of the adsorption structure, and discharging the feed water from the other end, and a ring member disposed between end portions on both sides of the outer tube and an inner surface of the housing.
Nanoparticle carrier platform and methods for controlled release of subterranean well treatment additives
Nano-sized mixed metal oxide carriers capable of delivering a well treatment additive for a sustained or extended period of time in the environment of use, methods of making the nanoparticles, and uses thereof are described herein. The nanoparticles can have a formula of:
A/[M.sub.x.sup.1M.sub.y.sup.2M.sub.z.sup.3]O.sub.nH.sub.m
where x is 0.03 to 3, y is 0.01 to 0.4, z is 0.01 to 0.4 and n and m are determined by the oxidation states of the other elements, and M.sup.1 can be aluminum (Al), gallium (Ga), indium (In), or thallium (Tl). M.sup.2 and M.sup.3 are not the same and can be a Column 2 metal, Column 14 metal, or a transition metal. A is can be a treatment additive.
Apparatus for removing chemotherapy compounds from blood
A filter apparatus for removing small molecule chemotherapy agents from blood is provided. The filter apparatus comprises a housing with an extraction media comprised of polymer coated carbon cores. Also provided are methods of treating a subject with cancer of an organ or region comprising administering a chemotherapeutic agent to the organ or region, collecting blood laded with chemotherapeutic agent from the isolated organ, filtering the blood laden with chemotherapeutic agent to reduce the chemotherapeutic agent in the blood and returning the blood to the subject.
Porous fiber, adsorbent material, and purification column
A solid fiber is described, where the solid fiber is characterized by (a) a modification degree Do/Di, in a cross section of the solid fiber of 1.20 to 8.50 where the inscribed circle diameter is denoted by Di and the circumscribed circle diameter is denoted by Do; and (b) a porous specific surface area of not less than 30 m.sup.2/g.
Super absorbent polymer and method for producing same
The super absorbent polymer comprises: a base polymer powder including a first crosslinked polymer of a water-soluble ethylenically unsaturated monomer having at least partially neutralized acidic groups; and a surface crosslinked layer formed on the base polymer powder and including a second crosslinked polymer in which the first crosslinked polymer is further crosslinked via a surface crosslinking agent, wherein the super absorbent polymer has: a fixed height absorption (FHA) of 22.5 g/g to 29 g/g, a saline flow conductivity (SFC) of 35 (.Math.10.sup.−7 cm.sup.3.Math.s/g) or more, and T-20 of 180 seconds or less.