Apparatuses and methods for extracting desired chemical species from input flows in a modular unit.

Apparatuses and methods for extracting desired chemical species from input flows in a modular unit.

A system that uses single or multiple elements arranged in a single unit or multiple arrays for the extraction, purification, and concentration of lithium and other constituents from a brine that can be constructed in a mobile unit.

A method for preparing a crude oil solution for analysis, including adding water to a porous adsorbent to obtain a supported water substrate, having a plurality of water monolayers disposed on the porous adsorbent. The method further includes exposing the crude oil solution to the supported water substrate for a period of time; separating the supported water substrate from the crude oil solution; washing the supported water substrate with a water immiscible solvent to remove at least one hydrocarbon; displacing water from the plurality of water monolayers and the at least one interfacially active compound from the porous adsorbent with an alcohol and a co-solvent to obtain a displaced phase. The displaced phase can include the water, the at least one interfacially active compound, the alcohol, and the co-solvent. Finally, the method can include drying the displaced phase to isolate the at least one interfacially active compound.

A non alpha controlled plating bath including Tin species and a trace amount of Polonium species is utilized in a plating tool. The plating tool includes a Polonium filter element to remove Polonium species from the plating bath to selectively plate Tin upon a plating cathode. The filter may include a Titanium inner portion surrounding by a stannic oxide exterior. The filter may reduce the Polonium species by having the polonium absorb and then enter within the stannic oxide matrix. The filter may be located within the plating tool reservoir or filter housing. The filter may be fabricated by forming Tin upon a Titanium backbone and converting the Tin to stannic oxide.

The invention provides an apparatus for polymer chromatography, comprising at least one column that comprises a first stationary phase comprising one of the following: A) a material comprising at least one non-carbon atom, excluding glass or a metal, selected from molybdenum sulfide MoS2, tungsten sulfide WS2, silicon carbide SiC, boron nitride BN, or combinations thereof, or B) glass, or a metal, or combinations thereof, and a material comprising at least one non-carbon atom selected from molybdenum sulfide MoS2, tungsten sulfide WS2, silicon carbide SiC, boron nitride BN, or combinations thereof. The invention also provides a method for polymer chromatography, comprising introducing a solution, comprising a polymer, into a liquid flowing through a first stationary phase, and wherein the first stationary phase comprises one of foregoing materials (A) or (B).

A methyl iodide adsorber, comprising a zeolite containing at least one iodide-adsorbing metal or a compound thereof, wherein the zeolite is a hydrophobic zeolite. Also, a use of the adsorber and a method for the adsorption of methyl iodide.

A particulate sorbent includes a carbonaceous and/of non-carbonaceous particulate matter encapsulated in sol-gel sorbent matrix where microparticles of a porous sol-gel metal oxide network display a high surface area with small cross-section pores and a nanoparticle or microparticle filler that is a carbonaceous and/or non-carbonaceous particulate matter. The particulate sorbent is prepared by dispersing carbonaceous and/of non-carbonaceous particulate matter in a mixture of a metal oxide precursor, water, catalyst and optionally a solvent and a polymer functionalized to react with the metal oxide precursor. Catalysis is by acid followed by base to separate hydrolysis in the sol with condensation to a gel to give a highly porous gel. The gel is subsequently fractured into sorbent particles. The sorbent particles can be used for sampling or separating analytes.

Provided are metal-organic frameworks made by the process of comprising the steps of reacting a first metal source that can generate a tetravalent metal cation in solution, a linear dicarboxylic acid, a second metal source that can generate a divalent cation in solution, and one or more monocarboxylic acid modulators in a solvent to provide a reaction solution. The reaction solution is heated to provide a metal-organic framework having between about 0 wt. % to 10 wt. % of divalent cation, surface area between about 1100 m.sup.2/g and 2700 m.sup.2/g, a porosity of between about 0.45 cc/g and 1.1 cc/g, and a relative intensity equal to or greater than 0.35 and a peak width ratio of less than 3.0.

A method for treating a liquid waste is provided. The method includes supplying the liquid waste to a plurality of cross flow filters from at least one high level waste tank; filtering the liquid waste via the plurality of cross flow filters to form a clarified salt solution; removing at least one radionuclide from the clarified salt solution via a plurality of elutable ion exchange columns filled with an ion exchange media to form an eluate and a decontaminated salt solution; and removing at least one radionuclide from the eluate via a first non-elutable adsorption component to form a dewatered radionuclide sorbent and a decontaminated eluate solution.