It is preferable that metallic sodium to be loaded to an engine valve used for an internal combustion engine such as automobile engine have high purity. However, conventionally, an organic solvent remaining in micropores on a surface of the metallic sodium have been hardly attracted attention. Provided is a method for purifying metallic sodium including steps of placing metallic sodium containing organic solvent in the micropores thereof in a melting tank which is sealed, and heating the melting tank under reduced pressure to vaporize and remove the organic solvent coating the metallic sodium.

Acquisition of critical minerals via refinement from aqueous sources. Technological and geopolitical advantagesinure to conflict-free refinement of rare materials including critical minerals used in production of energy storage devices, among other applications. Additionally, the applied clean tech methods advance environmental goals such as those given in the Paris Agreement. Various site-specific system configurations and corresponding site-specific methods of operation bring to bear a panoply of economically viable approaches to critical mineral refinement. In some approaches, electrical power needed to drive refinement is provided by selected site-specific renewable energy sources. Real-world implementations involve co-locating a dissociative reactor with a geothermal energy plant near a salar or other source (preferably aqueous) of critical minerals therein. Refined critical minerals are produced on site. Deployment of the various site-specific configurations of systems and practice of corresponding site-specific methods reduces or eliminates negative environmental impacts such as those incurred by legacy mining-based techniques.

A method includes treating a first brine stream including a plurality of minerals with an anti-scalant to produce a treated brine. The first brine stream is provided by a wastewater treatment system. The method also includes directing the treated brine to a first nanofiltration (NF) system disposed downstream from and fluidly coupled to the wastewater treatment system, generating a first NF permeate stream and a first NF non-permeate stream from the treated brine in the first NF system, directing the first NF non-permeate stream to a mineral removal system disposed downstream from and fluidly coupled to the first NF system, and removing the plurality of minerals from the first NF non-permeate stream to generate a first overflow stream in the mineral removal system. The first overflow stream comprises at least a portion of the plurality of minerals. The method also includes routing a first portion of the first overflow stream to a hydrochloric acid (HCl) and sodium hydroxide (NaOH) production system disposed downstream from and fluidly coupled to the mineral removal system. The HCl and NaOH production system includes a second NF system that may receive the first portion of the first overflow stream and may generate a second brine stream from the first portion of the first overflow stream. The method further includes directing the second brine stream to a first electrodialysis (ED) system disposed within the HCl and NaOH production system and fluidly coupled to the second NF system. The first ED system may generate HCl and NaOH from the second brine stream.

A method includes treating a first brine stream including a plurality of minerals with an anti-scalant to produce a treated brine. The first brine stream is provided by a wastewater treatment system. The method also includes directing the treated brine to a first nanofiltration (NF) system disposed downstream from and fluidly coupled to the wastewater treatment system, generating a first NF permeate stream and a first NF non-permeate stream from the treated brine in the first NF system, directing the first NF non-permeate stream to a mineral removal system disposed downstream from and fluidly coupled to the first NF system, and removing the plurality of minerals from the first NF non-permeate stream to generate a first overflow stream in the mineral removal system. The first overflow stream comprises at least a portion of the plurality of minerals. The method also includes routing a first portion of the first overflow stream to a hydrochloric acid (HCl) and sodium hydroxide (NaOH) production system disposed downstream from and fluidly coupled to the mineral removal system. The HCl and NaOH production system includes a second NF system that may receive the first portion of the first overflow stream and may generate a second brine stream from the first portion of the first overflow stream. The method further includes directing the second brine stream to a first electrodialysis (ED) system disposed within the HCl and NaOH production system and fluidly coupled to the second NF system. The first ED system may generate HCl and NaOH from the second brine stream.

The present invention refers to a process for removing Cs, and optionally Rb, from aqueous fluids including body fluids by fluorine containing reagents, the synthesis of fluorine containing, water-insoluble salts of said Cs isotopes and their use as therapeutic agents.

The present invention refers to a process for removing Cs, and optionally Rb, from aqueous fluids including body fluids by fluorine containing reagents, the synthesis of fluorine containing, water-insoluble salts of said Cs isotopes and their use as therapeutic agents.

Process to produce sodium carbonate from an ore mineral comprising sodium bicarbonate; comprising: dissolving sodium carbonate particles having a mean diameter D50, measured by sieve analysis, less than 250 m in a water solution; introducing the resulting production solution comprising sodium carbonate into less basic compartments of an electrodialyser comprising alternating less basic and more basic adjacent compartments separated from each other by cationic membranes; producing a solution comprising sodium hydroxide is produced into the more basic compartments; extracting the solution comprising sodium hydroxide from the more basic compartments of the electrodialyser and used to constitute a reaction solution; and putting the reaction solution into contact with the mineral ore comprising sodium bicarbonate in order to form a produced solution comprising sodium carbonate.

Process to produce sodium carbonate from an ore mineral comprising sodium bicarbonate; comprising: dissolving sodium carbonate particles having a mean diameter D50, measured by sieve analysis, less than 250 m in a water solution; introducing the resulting production solution comprising sodium carbonate into less basic compartments of an electrodialyser comprising alternating less basic and more basic adjacent compartments separated from each other by cationic membranes; producing a solution comprising sodium hydroxide is produced into the more basic compartments; extracting the solution comprising sodium hydroxide from the more basic compartments of the electrodialyser and used to constitute a reaction solution; and putting the reaction solution into contact with the mineral ore comprising sodium bicarbonate in order to form a produced solution comprising sodium carbonate.

Hydrometallurgical processes are provided for the recovery of metal values, including cesium, from epithermal mineral deposits, including pharmacosiderite-containing ores. Aspects of the process involve the preferential formation of a cesium alum, and preparation of cesium hydroxide from the cesium alum.

Hydrometallurgical processes are provided for the recovery of metal values, including cesium, from epithermal mineral deposits, including pharmacosiderite-containing ores. Aspects of the process involve the preferential formation of a cesium alum, and preparation of cesium hydroxide from the cesium alum.