A method of electrochemically treating a hydrocarbon-bearing formation is provided. The method includes electrochemically treating an aqueous fluid to provide a first fluid having a first electrochemical potential and a second fluid having a second electrochemical potential. The first electrochemical potential the second electrochemical potential have opposite signs. The method then includes introducing an amount of the first fluid into the hydrocarbon bearing formation, and then an amount of a spacer fluid is introduced into the hydrocarbon-bearing formation. An amount of the second fluid may be optionally introduced into the formation. The steps of introducing the fluids are repeated until an end point is reached. A system for electrochemically a hydrocarbon-bearing formation is also provided.

A method for preparing sodium taurine as a taurine intermediate is provided in the present disclosure. The method comprises the following steps: providing sodium hydroxyethyl sulfonate and an ammonia source; and placing the sodium hydroxyethyl sulfonate and the ammonia source in an aminolysis reactor for an aminolysis reaction to obtain a mixture containing sodium taurine as a taurine intermediate, wherein the molar ratio of ammonia in the ammonia source to the sodium hydroxyethyl sulfonate is greater than or equal to 25:1. A method for preparing taurine is further provided.

A treatment of demineralization effluents, particularly recycling effluents, a method for demineralizing whey and treating the effluents, and a facility for implementation thereof. The treatment of whey demineralization effluents includes: i) supplying a whey demineralization effluent, ii) treating by reverse osmosis effluent recovered in i) to obtain a reverse osmosis permeate and retentate, iii) neutralizing the retentate pH, iv) treating the neutralized retentate by nanofiltration to obtain a permeate including monovalent ions and a retentate including divalent ions and residual organic materials, v) treating the permeate in iv) by electrodialysis with bipolar membrane to obtain acidic solution(s) and basic solution(s). Thus, it is possible to treat effluents, limit their environmental impact, generate solutions for the whey demineralization process, reduce the cost of whey demineralization because some process water from electrodialysis comes from treatment of the generated effluents, and reduce the total amount of effluent sent to the wastewater treatment plant.

A preparation method of lithium hydroxide includes the following steps: A. coprecipitating a lithium extraction mother solution of salt lake brine with an aluminum salt solution and a sodium hydroxide solution, aging and then performing solid-liquid separation, washing and drying to obtain lithium aluminum hydrotalcite; B. acidifying the lithium aluminum hydrotalcite to obtain a lithium aluminate solution; C. performing nanofiltration on the lithium aluminate solution for lithium-aluminum separation, and sequentially performing primary concentration by reverse osmosis to obtain a primary concentrated lithium-rich solution; D. deeply removing aluminum from the lithium-rich solution to obtain an aluminum-removed lithium-rich solution; E. performing bipolar membrane electrodialysis on the aluminum-removed lithium-rich solution to obtain a secondary concentrated lithium-rich solution; F. evaporating the secondary concentrated lithium-rich solution for concentration to obtain lithium hydroxide.

A bipolar membrane comprising a first member comprising at least one anion exchange material; a second member comprising at least one cation exchange material, wherein the first member and the second member together form an interface junction; and disposed within the interface junction a first layer comprising a first water dissociation catalyst and a second layer comprising a second water dissociation catalyst, wherein the first water dissociation catalyst is different than the second water dissociation catalyst.

The disclosure relates to enhancing alkalinity of brine, e.g. seawater, using bipolar membrane electrodialysis (BPMED) without removing divalent cations that otherwise cause scaling. In one embodiment, a BPMED is employed wherein the brine volumetric flow rate through a basification compartment is greater at a given current density than that through a brine compartment which increases the pH of the brine output while keeping it below the precipitation pH. In one embodiment, the spacer located in the basification compartment is thicker than spacers elsewhere in the BPMED so as resist membrane distortion due to the increased hydrostatic pressure in the basification compartment given the greater volumetric flow. The brine output having increased alkalinity can be returned to the ocean to mitigate acidification and enable capture of atmospheric carbon dioxide.

A method for preparing battery grade and high purity grade lithium hydroxide and lithium carbonate from high-impurity lithium sources includes steps for preparation of a refined lithium salt solution, preparation of battery grade lithium hydroxide, preparation of high purity grade lithium hydroxide, preparation of high purity grade lithium carbonate and preparation of battery grade lithium carbonate. The system to carry out the preparation includes a refined lithium salt solution preparation subsystem, a battery grade lithium hydroxide preparation subsystem, a high purity grade lithium hydroxide preparation subsystem, a high purity grade lithium carbonate preparation subsystem and a battery grade lithium carbonate preparation subsystem arranged in turn according to production sequence. A combination of physical and chemical treatment methods are used to treat the high-impurity lithium sources having variations in lithium contents, impurity categories, and impurity contents.

There are provided processes for preparing a metal hydroxide comprising (i) at least one metal chosen from nickel and cobalt and optionally (ii) at least one metal chosen from manganese, lithium and aluminum, the process comprising: reacting a metal sulfate comprising (i) at least one metal chosen from nickel and cobalt and optionally (ii) at least one metal chosen from manganese, lithium and aluminum with lithium hydroxide, sodium hydroxide and/or potassium hydroxide and optionally a chelating agent in order to obtain a solid comprising the metal hydroxide and a liquid comprising lithium sulfate, sodium sulfate and/or potassium sulfate; separating the liquid and the solid from one another to obtain the metal hydroxide; submitting the liquid comprising lithium sulfate, sodium sulfate and/or potassium sulfate to an electromembrane process for converting the lithium sulfate, sodium sulfate and/or potassium sulfate into lithium hydroxide, sodium hydroxide and/or potassium hydroxide respectively; reusing the sodium hydroxide obtained by the electromembrane process for reacting with the metal sulfate; and reusing the lithium hydroxide obtained by the electromembrane process for reacting with the metal sulfate and/or with the metal hydroxide.

The present disclosure provides devices and methods of using same for cleansing a solution (e.g., a salt or used dialysis solution) of urea via electrooxidation, and more specifically to cleansing a renal therapy solution/dialysis solution of urea via electrooxidation so that the renal therapy solution/dialysis solution can be used or reused for treatment of a patient. In an embodiment, a device for the removal of urea from a fluid having urea to produce a cleansed fluid includes a urea decomposition unit and an electrodialysis unit.

A method of cleaning used dialysis fluid having urea to produce a cleaned dialysis fluid, the method including passing the used dialysis fluid having urea through a combination electrodialysis and urea oxidation cell, the cell including (i) a first set of electrodes for separation of the used dialysis fluid having urea into an acid stream and a basic stream, wherein the first set of electrodes includes an anode and a cathode; (ii) one or more second set of electrodes positioned to contact the basic stream with an electrocatalytic surface for decomposition of urea via electrooxidation, wherein the one or more second set of electrodes includes an anode and a cathode; and (iii) at least one power source to provide the first and second sets of electrodes with an electrical charge to activate the electrocatalytic surface.