Abstract: Disclosed is a method for the selective catalytic reduction of NOx in waste/exhaust gas by using ammonia provides by heating one or more salts of formula Ma(NH3)nXz, wherein M represents one or more cations selected from alkaline earth metals and transition metals, X represents one or more anions, a represents the number of cations per salt molecule, z represents the number of anions per salt molecule, and n is a number of from 2 to 12, the one or more salts having been compressed to a bulk density above 70% of the skeleton density before use thereof.

Abstract: Capturing at least one heavy metal, from mercury and arsenic, contained in a moist gas comprising water vapor, by the following steps: a) heating the moist gas by heat exchange with a compressed heat transfer fluid obtained in step e) in order to obtain a condensed heat transfer fluid and a gas reheated to a temperature Tc; b) bringing the reheated gas into contact with a heavy metal capture mass in order to obtain a gas depleted in heavy metal; c) decompressing the cooled heat transfer fluid; d) cooling the gas depleted in heavy metal by heat exchange with the heat transfer fluid produced in step c) in order to obtain a cooled gas at a temperature Tf, the heat transfer fluid being vaporized; e) compressing the vaporized heat transfer fluid in a manner such as to obtain a compressed heat transfer fluid, the compressed heat transfer fluid being recycled.

Abstract: The present disclose is directed to a method for controlling iodine levels in wet scrubbers, and, in particular, recirculating wet scrubbers by removing the iodine from the scrubbing solution, such as by using ion exchange, absorption, adsorption, precipitation, filtration, solvent extraction, ion pair extraction, and an aqueous two-phase extraction.

Abstract: An apparatus may have a selective catalytic reduction NOx catalyst including a high-temperature catalyst layer having high capability of reducing NOx at high temperatures and a low-temperature catalyst layer having higher capability of reducing NOx at low temperatures than that of the high-temperature catalyst layer. The low-temperature catalyst layer may be arranged closer to a catalyst substrate than the high-temperature catalyst layer. A supply valve may add an addition quantity of reducing agent for reducing NOx to exhaust gas flowing into the selective catalytic reduction NOx catalyst. A controller may comprise at least one processor configured to control addition of the reducing agent by the supply valve such that the reducing agent concentration in a reducing agent atmosphere formed in the exhaust gas flowing into the selective catalytic reduction NOx catalyst is higher when the temperature of the selective catalytic reduction NOx catalyst is in a specific low temperature range.

Abstract: A device, which is suitable for the processing of at least one fluid, is provided with at least one elongated foil, which is formed in a number of reciprocating foil layers. Between two opposite layers of foil, a spacer is situated that is permeable at least parallel to the foil layers. The foil layers and interposed spacers extend spirally around a central axis, wherein folding lines between two foil layers extend substantially parallel to the central axis. Each spacer is coupled to at least an end near the central axis with a support extending parallel to the central axis where, of the supports near the central axis, first supports are situated between two foil layers, which foil layers are connected to one another near the central axis, whereas second supports are situated between two successive first supports.

Abstract: A filter system comprises a hollow fiber membrane filter having pores; and an electrostatic adsorption filter partially or wholly having positive charges to be ion adsorbed with nanoparticles of negative charges by an electrostatic attraction, the nanoparticles which exist in the water, and the electrostatic adsorption filter configured to remove in advance the nanoparticles from the water to be supplied to the hollow fiber membrane filter, to prevent a water passing amount of the hollow fiber membrane filter from being rapidly reduced. According to the present invention, the viruses existing in raw water may be removed in accordance with a size exclusion mechanism of the hollow fiber membrane filter, and the nanoparticles, which cause the reduction of the water passing amount of the hollow fiber membrane filter, may be removed using the electrostatic adsorption filter.

Abstract: Disclosed herein is a method of preparing a nanoporous organic-inorganic hybrid film. The method includes preparing an organic sol including a compound having amino groups, a compound having isocyanate groups, and a solvent; adding an inorganic oxide precursor to the organic sol to form a mixed solution; and subjecting the mixed solution to heat treatment to form an organic molecule network structure in which the organic sol is gelled, and an inorganic molecule network structure located along a surface of the organic molecule network structure.

Abstract: A tubular braid, a hollow fiber membrane using the same, and a manufacturing method thereof. A hollow fiber membrane can maximize or increase adhesion between a polymer coating film and a tubular braid; significantly reduce degradation of film properties caused by non-uniform coating, that is, reduce leakage; obtain a higher percent rejection; and achieve high water permeability since the hollow fiber membrane has a larger inner diameter.

Abstract: Provided is a nonwoven fabric for semipermeable membrane support, in which adhesiveness of a semipermeable membrane to a support is satisfactory, the thickness uniformity of the semipermeable membrane is satisfactory, and permeation-through of a coating liquid does not occur.

Abstract: There is provided a composite gas separation membrane including a gas separation layer, which is formed to include a polyimide resin, on a support layer having gas permeability, in which the polyimide resin includes a repeating unit represented by the following Formula (I) in Formula (I), X represents a group having a specific structure represented by any of the following Formulae (I-a) to (I-h), in Formula (I), Y1 represents a group represented by the following Formula (II-a) or (II-b), and in Formulae (II-a) and (II-b), R3 represents a substituent group, A represents a dissociable group, p represents 0 or 1, p1 represents an integer of 0 to 2, and p2 represents an integer of 2 or greater.

Abstract: The present invention relates to a polyetherimide composite nanofiltration membrane and a preparation method thereof, the method comprises the following steps: (1) dissolving polyetherimide and an additive into an organic solvent, stirring and keeping aside for deaeration to prepare a casting solution, blade coating of the casting solution onto a smooth surface of a nonwoven fabric, and placing under an air atmosphere and then putting into deionized water to obtain a support membrane 1, wherein the surface of the nonwoven fabric coated with the casting solution is referred to as surface A; (2) immersing the surface A of the support membrane 1 into an aqueous solution of m-phenylenediamine, taking out and drying in the air, then immersing the surface A into a solution of 1,2,4,5-benzene tetracarbonyl chloride in n-hexane or cyclohexane, and taking out and drying in the air to obtain a support membrane 2; and (3) immersing the surface A of the support membrane 2 into an aqueous solution of EDC.

Abstract: A carbonated water production unit for a refrigerator includes a coupler to which a container is coupled to be detachable, a cylinder configured to store carbon dioxide, a nozzle module configured to inject carbon dioxide into the container, a regulation member, a first valve, a second valve, a user interface which receives a command for production of carbonated water and an input of concentration of the carbonated water, and a controller which controls the first valve to supply water when the command for the production of carbonated water is input, determines information on injection of the carbon dioxide corresponding to the concentration of the carbonated water when the supply of water is completed, controls the regulation member to inject the carbon dioxide based on the determined information on the injection, and controls the second valve to regulate the pressure of the container when injection of the carbon dioxide is completed.

Abstract: A device for storing and mixing bone cement components. The device includes a housing, a safety device, and a vacuum indicator. The housing defines a mixing chamber configured to store a first bone cement component therein. In a first safety position, the safety device prevents contact between the first bone cement component and a second bone cement component in the mixing chamber. In a second safety position, the safety device permits contact between the first and second bone cement components in the mixing chamber. The vacuum indicator restricts movement of the safety device from the first safety position to the second safety position when in a first vacuum indicator position. The vacuum indicator permits movement of the safety device from the first safety position to the second safety position when in a second vacuum indicator position.

Abstract: An azeotropic or quasi-azeotropic composition including hydrogen fluoride, 3,3,3-trifluoro-2-chloropropene and one or more (hydro)halogen-carbon compounds including between 1 and 3 carbon atoms. Also an azeotropic or quasi-azeotropic composition including hydrogen fluoride, 3,3,3-trifluoro-2-chloropropene, and one or more compounds selected from among 1,3,3,3-tetrafluoropropene, 1,1,1,2,2-pentafluoropropane, 2,3,3,3-tetrafluoropropene, 3,3,3-trifluoropropene, E-3,3,3-trifluoro-1-chloropropene, trifluoropropyne, 1,1,3,3-pentafluoropropane, 1,1,1,3,3-pentafluoropropane, 1,1,1,3,3-pentafluoropropene, 1,1,1,2,3-pentafluoropropene and 2-chloro,1,1,1,2-1 tetrafluoropropane.

Abstract: The present disclosure is directed to compositions having lecithin, a plasticizer, and an emulsifier. The composition may be used solubilize polar solvents in non-polar liquids. Methods of producing and using the compositions disclosed herein are also disclosed.

Abstract: A fluidized fuel gas combustor system for a catalytic dehydrogenation process comprising a vessel having a lower portion and an upper portion; a plurality of air injection diffusers located in the lower portion of the vessel; a plurality of fuel gas injection diffusers located on fuel gas distributors disposed in the vessel and spaced apart from and above a plurality of air injection diffusers, wherein the fuel gas diffusers are placed in a manner to maximize even mass distribution of a fuel gas injected through the fuel gas diffusers in the vessel, wherein each fuel distributor comprises a tube having a plurality of fuel gas injection diffusers; and one or more grid assemblies disposed in the vessel spaced above the fuel gas distributors is provided.

Abstract: A method for managing the charging of a space with solid particles, comprising: modelling an expected charging profile over a charging duration, during the charging, receiving, from at least one sensor, measured values of a parameter indicative of the height of a bed of solid particles charged into the space, determining filtered values of the parameter indicative of the height from the measured values received and from the modelled charging profile, and transmitting the filtered values to control the charging with solid particles.

Abstract: A feed injector for a circulating fluid bed reactor is fitted with a discharge nozzle with a circular, radially notched discharge orifice to improve the surface-to-volume ratio of the spray pattern formed by the nozzle. The feed injector is useful for injecting fluids into various types of circulating fluid bed reactors in which good contact between the components of the fluidized bed and the injected fluid is required. It is particularly useful in fluid coking reactors.

Abstract: A method for recovering hydrochloric acid and metal oxides from a chloride liquor is described. The method uses a chloride liquor including the metal and mixing the liquor and a matrix solution to produce a reaction mixture, wherein the matrix solution assists oxidation/hydrolysis of the metal with HCl production. In a preferred embodiment the matrix solution includes zinc chloride in various stages of hydration and an oxygen containing gas is added to the mix. A method where the improvement is the mixing of a liquor and a matrix solution where the solution assists hydrolysis of the metal with HCl production is also disclosed. The reactor is a column reactor in a preferred embodiment. Further disclosed is the method of using the matrix solution and a reactor for recovering hydrochloric acid and for oxidizing/hydrolysis of a metal.

Abstract: Methods and compositions are disclosed relating to the localization of nucleic acids to arrays such as silane-free arrays, and of sequencing the nucleic acids localized thereby.

Abstract: De novo synthesized large libraries of nucleic acids are provided herein with low error rates. Further, devices for the manufacturing of high-quality building blocks, such as oligonucleotides, are described herein. Longer nucleic acids can be synthesized in parallel using microfluidic assemblies. Further, methods herein allow for the fast construction of large libraries of long, high-quality genes. Devices for the manufacturing of large libraries of long and high-quality nucleic acids are further described herein.

Abstract: A method for producing a radionuclide is provided that produces molybdenum trioxide 99 (Mo-99.O3) and technetium oxide 99m (Tc-99m2.O7) by emitting an electron beam accelerated by an electron linear accelerator to a molybdenum trioxide 100 (Mo-100.O3) powder sample, and which separates and purifies technetium oxide 99m from both the molybdenum trioxide 99 and the technetium oxide 99m by using a radionuclide separation/purification unit. The method for producing a radionuclide supplies temperature-regulated gas to the molybdenum trioxide 100 powder sample during an irradiation period during which the electron beam is emitted to the molybdenum trioxide 100 powder sample.

Abstract: Provided are an adsorbent for trapping a radioactive iodine gas generated in a process of oxidizing a nuclear fuel at a high temperature after use and a method of preparing the same, and more particularly, a radioactive iodine gas adsorbent which is formed of bismuth as a main component, thereby exhibiting an excellent radioactive iodine gas trapping capability and an excellent thermal stability after trapping, and a method of preparing the same. An adsorbent for trapping a radioactive iodine gas prepared by a method of preparing an adsorbent for trapping a radioactive iodine gas according to the present disclosure may effectively trap a radioactive iodine off-gas generated in a nuclear fuel pre-treated oxidizing process after use. Particularly, the adsorbent may trap iodine in a larger amount, which is twice or more, than a silver-containing zeolite widely used to trap a radioactive iodine gas, and the trapped iodine forms a stable compound, which is more advantageous for long-term storage.

Abstract: Hygroscopic particles including a crosslinked polymer containing 6.0 to 12.0 meq/g of carboxyl groups and 0.1 to 2.0 meq/g of sulfonic acid groups and/or sulfonate groups, 80% or more of the carboxyl groups being neutralized to a potassium salt.

Abstract: Provided is a temperature-responsive hygroscopic material having a hygroscopic property that varies widely according to temperature variation and a method for producing the temperature-responsive hygroscopic material. The temperature-responsive hygroscopic material includes a mesoporous body having an average pore diameter of 2 nm to less than 50 nm and a temperature sensitive molecule chemically bonded with the mesoporous body inside a pore of the mesoporous body. The method includes a step of causing, in a solvent including an activator and a coupling agent, a coupling reaction of: a mesoporous body having an average diameter of 2 nm to less than 50 nm and having a functional group on a surface thereof; and a temperature sensitive molecule having a functional group which can undergo a coupling reaction with the functional group on the surface of the mesoporous body.

Abstract: A process for the preparation of a calcined mixed oxide comprising Al-, Ce- and Zr-oxides, comprising the steps of providing an aqueous slurry comprising hydroxides of cerium and zirconium, contacting the hydroxides of cerium and zirconium with an alumina precursor to obtain an aqueous suspension of solids, isolating the solids from the aqueous suspension and drying to obtain a solid composition, calcining the solid composition of step (c) at a temperature from 450° C. to 1200° C. for at least 1 hour to obtain a calcined mixed oxide.

Abstract: An alkaline catalyst for hydrogen generation can comprise a first metal (102), a second metal (104), and hydroxide (104). When the alkaline catalyst is added to an aqueous solution containing a hydrogen generation metal, the aqueous solution produces at least 4 L of hydrogen per 5 gram of hydrogen generation metal per 15 minutes at a production temperature of 140° F. and at a pressure of 1 atm.

Abstract: The process provided herein is concerned with disposal of oxidized sulfur compounds formed by oxidative desulfurization. The process uses solid base catalyst in the presence of a caustic solution or solid base catalyst pretreated with a base and eliminates the need to separate the sulfones from the hydrocarbon streams and recover the hydrocarbons.

Abstract: A method for producing chlorine by oxidizing hydrogen chloride with oxygen in the presence of a catalyst, wherein the catalyst satisfies the following conditions (i) and (ii): (i) the BET specific surface area is from 1 to 250 m2/g; and (ii) the value of H/D, wherein H is the half width of the peak of a pore distribution curve as determined by a mercury intrusion method; and D is the average pore diameter, is from 0.6 to 1.5.

Abstract: An objective of the present invention is to provide a method for producing a catalyst for exhaust gas removal having excellent heat tolerance and purification performance within a wide range of atmospheres and a catalyst obtained by the production method. The present invention relates to a method for supporting catalyst metal particles, comprising: (a) adding an iridium precursor and a palladium precursor to a solvent containing at least one member selected from the group consisting of polyvinylpyrrolidone, N-methylpyrrolidone, N-vinyl-2-pyrrolidone, and ethylene glycol; (b) adding a reducing agent to the obtained catalyst metal colloid; (c) obtaining a concentrated solution containing catalyst metal particles by subjecting the obtained solution to heat reflux; and (d) supporting the catalyst metal particles on a carrier, wherein the iridium content of the catalyst metal particles accounts for 3% to 10% by mass of the total mass of iridium and palladium.

Abstract: Disclosed is a method for manufacturing a homogeneous supported catalyst for carbon nanotubes. Advantageously, the method induces deep impregnation of a catalyst in micro pores of a support by using high-temperature aging impregnation, thus providing a high CNT yield.

Abstract: The present invention provides a process and catalyst for the autothermal and dry reforming of methane to produce syngas. The process provides a direct single step gas phase reforming of methane or natural gas to syngas over Ni—Pt supported nanocrystalline ZrO2. The process provides methane conversion of 54-99% with H2/CO ratio of 1.14 to 1.42 (mol %) in the temperature range of 250 to 750 800° C. at atmospheric pressure.

Abstract: Hydroxypropionic acid, hydroxypropionic acid derivatives, or mixtures thereof are dehydrated using a catalyst and a method to produce bio-acrylic acid, acrylic acid derivatives, or mixtures thereof. A method to produce the dehydration catalyst is also provided.

Abstract: The chabazite-type zeolite of the present invention has a SiO2/Al2O3 molar ratio of less than 15, and an average particle size from 1.0 ?m to 8.0 ?m. The chabazite-type zeolite of the present invention has excellent durability and heat resistance, and the copper-loaded chabazite-type zeolite has an improved NOx reduction rate at low temperatures compared to conventional copper-loaded chabazite-type zeolite.

Abstract: Described is a selective catalytic reduction catalyst comprising a zeolitic framework material of silicon and aluminum atoms, wherein a fraction of the silicon atoms are isomorphously substituted with a tetravalent metal. The catalyst can include a promoter metal such that the catalyst effectively promotes the reaction of ammonia with nitrogen oxides to form nitrogen and H2O selectively over a temperature range of 150 to 650° C. A method for selectively reducing nitrogen oxides and an exhaust gas treatment system are also described.

Abstract: The present disclosure relates to a preparing method of a zeolite core/silica zeolite shell composite, which includes adding a zeolite seed crystal into a gel solution containing a silicon-source compound, a structure directing agent and a fluorine anion-source compound, and then, crystallizing the gel solution for growing a silica zeolite shell containing a crystal structure which is coherent with that of the zeolite seed crystal; a zeolite core/silica zeolite shell composite prepared by the preparing method above; and catalytic use of the zeolite core/silica zeolite shell composite.

Abstract: The present invention relates to a heavy oil catalytic cracking catalyst having a high yield of light oil and preparation methods thereof. The catalyst comprises 2 to 50% by weight of a magnesium-modified ultra-stable rare earth type Y molecular sieve, 0.5 to 30% by weight of one or more other molecular sieves, 0.5 to 70% by weight of clay, 1.0 to 65% by weight of high-temperature-resistant inorganic oxides, and 0.01 to 12.5% by weight of rare earth oxide. The magnesium-modified ultra-stable rare earth type Y molecular sieve is obtained by the following manner: the raw material, a NaY molecular sieve, is subjected to a rare earth exchange, a dispersing pre-exchange, a magnesium salt exchange modification, an ammonium salt exchange for sodium reduction, a second exchange and a second calcination. The catalyst provided in the present invention is characteristic in its high conversion capacity of heavy oil and a high yield of light oil.

Abstract: A method for synthesizing small crystals of silicoaluminophosphate-34 (SAPO-34) molecular sieves with high structural purity. The method includes forming a first slurry and a second slurry which are aged separately to form a first aged slurry and a second aged slurry. The first slurry includes a first source of phosphorus, a first source of aluminium, a first source of silicon, and at least one first organic structure directing agent. The second slurry includes a second source of phosphorus, a second source of aluminium, a second source of silicon, and at least one second organic structure directing agent. Then, the first aged slurry and the second aged slurry are combined to form a mixture of aged slurries. Finally, crystallization of silicoaluminophosphate molecular sieves comprising the SAPO-34 molecular sieves is induced from the mixture of aged slurries.

Abstract: A reagent preparation and dispensing device includes a body having a reaction chamber for a reagent and a solution reservoir for a solution. The solution reservoir is isolated from the reaction chamber. A plunger is movably coupled with the body. Movement of the plunger from a starting position to a seated position pushes the solution into the reaction chamber. A dispensing path extends from the reaction chamber out of the body. The dispensing path is configured to dispense a reagent mixture formed from the solution and the reagent. A vent path extends from the reaction chamber, the vent path vents reaction chamber gas displaced by the addition of the solution to the reaction chamber throughout movement of the plunger from the starting position to the seated position.

Abstract: A sample analyzer including a reagent reservoir configured to store a plurality of reagent containers; a first reagent dispenser configured to aspirate reagent of a first type from the reagent reservoir and dispense the aspirated reagent into a reaction container disposed at a first dispensing position; a second reagent dispenser configured to aspirate reagent of a second type from the reagent reservoir and dispense the aspirated reagent into a reaction container disposed at a second dispensing position; and a support member configured to support the first and the second reagent dispensers; wherein the first and the second reagent dispensers are supported by the support member so as to be movable independently of each other between each dispensing position and the reagent reservoir is disclosed. A sample analyzing method executed by a sample analyzer is also disclosed.

Abstract: An analysis tool suppressing background and improving detection sensitivity. In a first plate is formed a first concavity having, in the path of excitation light of a surface opposite to a bonding surface, a first bottom surface, a first opening, and a slanted surface widening from the edge of the first bottom surface towards the edge of the first opening. In a second plate, having a flow path formed on the bonding surface, is formed a second concavity having, in the path of excitation light of the surface opposite to the bonding surface, a second bottom surface, a second opening, and a slanted surface widening from the edge of the second bottom surface towards the edge of the second opening. The first plate is bonded to the second plate, and the first opening and the second opening are covered with a film.

Abstract: Biological activity in holding pens in a micro-fluidic device can be assayed by placing in the holding pens capture objects that bind a particular material of interest produced by the biological activity. The biological material of interest that binds to each capture object can then be assessed, either in the micro-fluidic device or after exporting the capture object from the micro-fluidic device. The assessment can be utilized to characterize the biological activity in each holding pen. The biological activity can be production of the biological material of interest. Thus, the biological activity can correspond to or arise from one or more biological cells. Biological cells within a holding pen can be clonal cell colonies. The biological activity of each clonal cell colony can be assayed while maintaining the clonal status of each colony.

Abstract: The present invention provides microfabricated substrates and methods of conducting reactions within these substrates. The reactions occur in plugs transported in the flow of a carrier-fluid.

Abstract: Provided are a reagent supply method and device capable of using up a reagent in a container without a remnant to the extent possible, and supplying the reagent to an analysis device without mixing air bubbles even when the remaining amount of the reagent is extremely small. The reagent supply device includes: at least one reagent container including: a container body for storing a liquid reagent; and a reagent supply port arranged on the container body; and a support member for supporting the at least one reagent container so that the reagent supply port is positioned on a lower side of the container body. The reagent supply port is sealed by a plug including at least one nozzle penetration portion. The at least one nozzle penetration portion is formed of a material having a Shore hardness of from A5° to A90°.

Abstract: A thermal cycling device for performing nucleic acid amplification on a plurality of biological samples positioned in a sample well tray. The thermal cycling device includes a sample block assembly, an optical detection system, and a sample well tray holder configured to hold the sample well tray. The sample block assembly is adapted for movement between a first position permitting the translation of the sample well tray into alignment with sample block assembly, and a second position, upward relative to the first position, where the sample block assembly contacts the sample well tray. A method of performing nucleic acid amplification on a plurality of biological samples positioned in a sample well tray in a thermal cycling device is also provided.

Abstract: The present disclosure provides fully integrated microfluidic systems to perform nucleic acid analysis. These processes include sample collection, nucleic acid extraction and purification, amplification, sequencing, and separation and detection. The present disclosure also provides optical detection systems and methods for separation and detection of biological molecules. In particular, the various aspects of the invention enable the simultaneous separation and detection of a plurality of biological molecules, typically fluorescent dye-labeled nucleic acids, within one or a plurality of microfluidic chambers or channels. The nucleic acids can be labeled with at least 6 dyes, each having a unique peak emission wavelength. The present systems and methods are particularly useful for DNA fragment sizing applications such as human identification by genetic fingerprinting and DNA sequencing applications such as clinical diagnostics.

Abstract: A powder classification apparatus (10; 110; 210) includes a first chamber (12; 112; 212) that includes a fluidized bed and has an inlet (16; 116; 216A) and an outlet (18; 118; 218), the inlet (16; 116; 216A) configured to receive a gas (G) and distribute the gas (G) in a uniform flow through the first chamber (12; 112; 212), the first chamber (12; 112; 212) configured to receive a powder (P) and the gas (G) and create a fluidization zone, the outlet (18; 118; 218) configured to allow at least a portion of the powder (P) to exit the first chamber (12; 112; 212); and a second chamber (14; 114; 214) having a powder inlet (24; 124; 224) configured to accept at least a portion of the powder (P) from the outlet (18; 118; 218) in the first chamber (12; 112; 212) caused by at least a portion of the powder (P) being ejected from the first chamber (12; 112; 212) by the gas (G).

Abstract: A waste gas is contacted with a mercury removal agent to remove mercury and a flue gas conditioning agent to alter a resistivity and/or cohesivity of particulates. The flue gas conditioning agent can be substantially free of SO3and/or comprise more than about 25 wt. % SO3, and/or the mercury removal agent can be substantially unaffected by the flue gas conditioning agent. An amount of mercury removed from the waste gas in the presence of the flue gas conditioning agent can be the same or more than that removed from the waste gas in the absence of the flue gas conditioning agent. An amount of the acid gas removed, by an acid gas removal agent, from the waste gas in the presence of the flue gas conditioning agent can be the same or more than that removed from the waste gas in the absence of the flue gas conditioning agent.

Abstract: There is provided methods for separating a target material from a raw material by mixing the raw material with water to form a slurry, adding a collector compound to the slurry to modify a relative hydrophobicity of a surface of the target material, adding a facilitator compound to enhance the modification of the relative hydrophobicity of the surface, and forming a froth including a concentrate of the target material. Disclosed methods may also include adding a facilitator compound to a raw material slurry that has been treated with a collector compound and a reagent for neutralizing the collector compound.

Abstract: A centrifugal separation apparatus includes a plurality of centrifugal separators each comprising a rotator which supports a plurality of sample containers containing a sample therein, a base in which the centrifugal separators are arranged in columns and stages and a route is defined therein, the centrifugal separators being movable inside the base, and a movement mechanism that sequentially move the centrifugal separators along the route in the base.