Patent classifications
B01J20/28011
Evaporative emission control articles including activated carbon
A coated substrate (2a, 2b) adapted for hydrocarbon adsorption having at least one surface, and a coating on the at least one surface, the coating comprising particulate carbon and a binder, wherein the particulate carbon has a BET surface area of at least about 1300 m.sup.2/g; and at least one of: (i) a butane affinity of greater than 60% at 5% butane; (ii) a butane affinity of greater than 35% at 0.5% butane; (iii) a micropore volume greater than about 0.2 ml/g and a mesopore volume greater than about 0.5 ml/g. A bleed emission scrubber (1) and an evaporative emission control canister system (30) comprising the coated substrate (2a, 2b) are provided. They can control evaporative hydrocarbon emissions and may provide low diurnal breathing loss (DBL) emissions even under a low purge condition.
ABSORBENT MATERIAL, WATER ABSORBENT AND METHOD FOR PRODUCING WATER ABSORBENT
Provided are: a water-absorbing agent achieving, in a balanced manner, both good physical properties and a decrease in speed of coloration with lapse of time even if the water-absorbing agent has a high moisture absorbing speed due to having a large specific surface area; and an absorbent body having a low ratio of pulp and achieving, in a balanced manner, both good physical properties suitable for a thin disposable diaper and a decrease in speed of coloration with lapse of time. The absorbent body contains a hydrophilic base material and a water-absorbing agent which contains: surface-crosslinked water-absorbing resin particles having a non-uniformly pulverized shape; α-hydroxycarboxylic acid (salt); and an aminocarboxylic acid-based chelating agent and/or a phosphorus-based chelating agent, a point plotted along an x-axis that represents an amount (x.sub.1 mol %) of α-hydroxycarboxylic acid (salt) extracted from the water-absorbing agent and along a y-axis that represents an amount (y.sub.1 mmol %) of an aminocarboxylic acid-based chelating agent and/or a phosphorus-based chelating agent extracted from the water-absorbing agent being within a range that satisfies a specific relational formula of x.sub.1 and y.sub.1, the water-absorbing agent having a moisture absorbing speed of 120 mg/g/hr or more at a temperature of 40±1° C. at a relative humidity of 75±1% RH.
Preparation of Magnetic Core-Shell Particles
The invention relates to a process for preparing core-shell particles comprising the steps of (i) providing a dispersion of primary magnetic particles having a mean diameter lower than 200 nm in a solvent; (ii) adding one or more (semi-)metal (oxyhydr)oxide(s) and/or one or more precursor(s) of a (semi-)metal (oxyhydr)oxide to said dispersion; (iii) optionally adding a hydrolysis agent for said one or more precursor(s); (iv) injecting the dispersion in a spray dryer; whereby a (semi-)metal (oxyhydr)oxide shell is formed on the magnetic particles during spray drying. The invention also relates to particles obtainable by said process, to a formulation of said particles in a solvent and to the use of said particles or said formulation for RNA or DNA extraction.
Extruded granular absorbent
Extruded granular sorbent formed of sorbent granules each being or including an extruded pellet containing water soluble binder sufficient to self-clump when wetted producing clumps of granules each having a clump retention rate of at least 90% and which shrink after clump formation during drying producing a nonstick clump that condenses pulling away from any contacting solid surface minimizing adhesion therebetween. Such clumps preferably also have a crush strength of at least 15 PSI when dry. Pellets preferably contain cold water-soluble amylopectin binder that not only solubilizes when wetted to facilitate clumping but which also opens the interior of the pellet improving absorption capacity. Sorbent well suited for use as litter is formed of granules or pellets having sizes falling within a plurality of different size ranges with the smaller sized fines causing the clumps to form on top of the litter extending generally horizontally along the litter.
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°.
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.
Ultra-high performance and high purify biogenic silica filtration media
This disclosure relates to ultra-high performance diatomite products possessing very high silica specific volume, a characteristic which provides for high filtration performance, in terms of low unit consumption and long filtration cycle times. These novel products of this disclosure also show very low extractable metals for both the non-acid washed and the high purity (acid washed) grades. These characteristics are of particular value in the separation of solids from high purity liquids in electronic chemical, specialty beverage and life science applications. In addition to outstanding physical and chemical characteristics, these products also contain no detectable levels of cristobalite and have a wide range of permeabilities, and are produced from mineralogically impure ores containing high levels of alumina and iron oxide.
Removal of bacteria from drinking water via filtration
The present invention relates to a method for producing biocidal, porous particles of a cross-linked polymer, and to the porous particles that can be produced according to the method of the invention. The invention further relates to porous particles of an amino-group-containing polymer (polyamine) having a relatively low swelling factor. The porous particles according to the invention are used to remove biological contaminants from water and to bind metal-containing ions from solutions. The present invention further relates to a filter cartridge which contains the porous cross-linked polymer particles according to the invention.
Material phase with electrical lead
A chromatograph is provided for identifying components of a mixture. Components are identified by different rates of adsorption and/or desorption with a material phase. In one embodiment, an electrical lead is connected to the material phase for supplying an electrical charge to the material phase. The electrical charge alters the rate of adsorption/desorption of the components with the material phase. In another embodiment, the material phase is disposed between two conductors with electrical leads connected to each of the conductors. A charge differential between the two conductors alters the rate of adsorption and/or desorption of components with the material phase.