Patent classifications
B01J20/3042
System and ultrahigh pressure extrusion method for making extruded granular sorbent with post-extrusion cold-processing of extruded granular absorbent for size control
A post-extrusion extruded granular sorbent processing system having a pellet-collecting enclosure that receives pellets of granular sorbent extruded from a starch-containing admixture through a die at a discharge end of an extruder and transports the pellets in air from an air mover flowing from the enclosure through a pellet-conveying duct of a pneumatic conveyor cooling and drying the pellets. The system includes a subsystem configured for processing the pellets after extruding, cooling, and drying using a pellet processing machine configured for reducing a size of each pellet having a size greater than a size reduction setting of the machine. A preferred pellet processing machine has rotating horizontally and circumferentially corrugated rollers with a selectively variable gap between the rollers providing the size reducing setting and configuring the rotating rollers for reducing a size of the pellets passing between the rollers having a size greater than the gap between the rollers.
ENHANCEMENT OF REDUCTION RESISTANCE FOR MANGANESE OXIDE ADSORBENTS
Processes for removing arsenic compounds from a feed stream using an adsorbent in disclosed. The process includes contacting a feed stream comprising at least arsenic and sulfur compounds with an adsorbent comprising an low-crystallinity manganese oxide, at least one halide and a binder, to provide a treated effluent substantially free of the arsenic and sulfur compounds.
ACTIVE CARBON MOLDED BODY
An active carbon molded body that comprises a plurality of active carbon granules that are formed from aggregates of active carbon particles. The active carbon granules include a fibrous granulation binder. The active carbon molded body is formed as a result of the plurality of active carbon granules being aggregated by means of the fibrous granulation binder in the active carbon granules.
The present invention is also an active carbon molded body production method in which active carbon granules that have been formed by aggregating active carbon particles by means of a fibrous binder are molded by simultaneous application of heat and pressure without separate addition of a molding binder.
The present invention thereby provides: an active carbon molded body that has high purification capacity and good production efficiency; and a production method for the active carbon molded body.
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.
Adsorbent, Canister and Method for Producing Adsorbent
An adsorbent to be packed into a canister, at least containing activated carbon and an additive material that has a higher heat capacity than the activated carbon. The adsorbent has first pores derived from the activated carbon that are less than 100 nm and second pores derived from meltable cores that are 1 μm or more. The adsorbent is in the form of a hollow molded body having an outer diameter of more than 6 mm and not more than 50 mm and including a cylindrical wall and honeycomb walls each having a thickness of not less than 0.2 mm and not more than 1 mm. The adsorbent has a volumetric specific heat of 0.08 kcal/L.Math.° C. or more. The ratio of the volume of the second pores to the volume of the first pores is not less than 10% and not more than 200%.
Process for the production of copper sulfide
A process for preparing a copper sulfide of the formula Cu.sub.xS.sub.y, wherein the process comprises the following steps: (i) reacting an aqueous solution of a copper salt with a molar excess of a sulfiding agent so as to precipitate copper sulfide from the solution; (ii) isolating the copper sulfide precipitate from the reaction mixture; and (iii) drying the copper sulfide precipitate at a temperature of less than 100° C., wherein x and y are integer or non-integer values.
Biochars, biochar extracts and biochar extracts having soluble signaling compounds and method for capturing material extracted from biochar
A method for capturing material extracted from biochar is provided comprising the steps of: (i) providing a biochar; (ii) contacting the biochar with an extraction media, where the extraction media causes the removal of residual compounds from the pores and surface of the biochar, creating a resulting extract comprised of the extraction media and removed compounds; and (iii) collecting the resulting extract. The method also can include other steps of extraction and purification. The method further comprises the step of applying the resulting extract to seeds, plants, soil, other agricultural products, or for use in other applications. A biochar having high levels of soluble signaling compounds is also provided, where the biochar is derived from a biomass source that together with predefined pyrolysis parameters produces resulting biochar having increased levels of soluble signaling compounds that are known to increase seed germination rates and early plant growth. Such soluble signaling compounds can then be collected in a biochar extract by contacting the biochar with an extraction media.
PACKING MATERIAL FOR ION CHROMATOGRAPHY AND PRODUCTION METHOD THEREFOR
A packing material for ion chromatography has a structure in which a polyethyleneimine is bonded, directly or through a spacer, to a surface of an organic porous substrate constituted of a hydroxylated crosslinked copolymer, and a functional group represented by formula (1)
##STR00001##
(wherein the symbols are as described in the description) is bonded to a nitrogen atom derived from the polyethyleneimine. The invention further relates to a production method of the packing material for ion chromatography and a column for ion chromatography. A packing material is provided for a column which exhibits a high separating performance in anion chromatography employing a hydroxide-based eluent, and a production method thereof is also provided.
HOLLOW CORE GRANULES, PRODUCTS INCORPORATING THE GRANULES, AND METHODS OF PREPARING THE GRANULES
The present disclosure relates to hollow core granules, products incorporating the hollow core granules, and methods of making the hollow core granules. The hollow core granules can comprise at least one wall surrounding a cavity that is devoid of any solid or liquid so as to define a hollow core, the at least one wall comprising a plurality of individual particles of at least one wall forming material, the plurality of individual particles sufficiently bound together so that the at least one wall is structurally self-sustaining. The hollow core granules further can include a binder material present in the at least one wall. The hollow core granules can be useful as a standalone material and/or may be useful in preparing a variety of products wherein the hollow core granules may be mixed or otherwise combined with further components. The disclosure further provides methods of making such hollow core granules.
SINTERED BODY FOR ADSORPTION, PRODUCTION METHOD THEREFOR, AND ADSORPTION DEVICE
To adsorb a substance to be treated in a fluid (7) with a higher adsorption capacity and lower pressure loss, an adsorptive sintered compact (20) includes powder adsorbent materials (1a, 1b), and resin structures (2) in which voids (3) are formed in a three-dimensional network. The powder adsorbent materials (1a, 1b) include free adsorbent materials (1a) free-movably contained in the voids (3) between the resin structures (2), and fixed adsorbent materials (1b) fixed to a surface (2a) of the resin structure (2) and/or at least partly embedded inside the resin structure (2), and the powder adsorbent materials (1a, 1b) are at least one of powdered activated carbon, powdered activated clay, and zeolite.