The present disclosure relates to the field of making high molecular weight adenosine-based coenzymes available on a large scale. In particular, it relates to a method for purifying high molecular weight adenosine-based coenzymes by implementing a tangential diafiltration, or even dia-ultrafiltration step. This method is, for example, applicable to the purification of coenzyme A disulfide ((CoAS).sub.2), coenzyme A (CoA), nicotinarnide adenine dinucleotide (NAD+), nicotinarnide adenine dinucleotide phosphate (NADP.sup.+) or flavin adenine dinucleotide (FAD).

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, copper, magnesium 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, copper, magnesium 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.

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 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.

The present disclosure provides a method and a system for extracting long chain dicarboxylic acid, the method comprising: (1) subjecting a long chain dicarboxylic acid fermentation broth to a primary membrane filtration treatment to give a first filtrate; subjecting the first filtrate to decolorization, acidification/crystallization, and solid-liquid separation treatments to give a first solid; (2) mixing the first solid, a base and water to form a solution; subjecting the solution to a secondary membrane filtration treatment to give a second filtrate; subjecting the second filtrate to decolorization, acidification/crystallization, and solid-liquid separation treatments to give a second solid; and (3) mixing the second solid and water to form a mixture; subjecting the mixture to a thermostatic treatment at 105-150° C., followed by cooling for crystallization and solid-liquid separation treatment. By the method, the resulted long chain dicarboxylic acid product has a high purity and no residual organic solvent.

A method for the treatment of water using reverse osmosis (RO) membranes and nano-filtration membranes wherein the permeate of the membranes is fluid connected to a feed water source via a pressurized storage buffer tank as well as to the fluid connection to use, the method comprising the steps of supplying treated water through a sanitary fully pressurized buffer tank, and supplying waste water through a recirc loop which contains recirculated concentrate and storing treated water in the buffer tank with low total dissolved solids of less than 10% of feed water, low pH of less than pH 7, and of low total organic carbon of less than 25% of feed water ensuring sanitary storage. It further includes opening a waste valve in the recirc loop which purges recirculated concentrate in order to rapidly reduce the conductivity of the water in the recirc loop. It further includes the steps of operating the waste valve such that it maintains the conductivity of the recirculated waste water in the recirc loop within a pre selected range of values and opening the waste valve when a measured conductivity setpoint is exceeded, and closing the waste valve when a measured conductivity setpoint is met.

The present invention is directed to a method of producing active pharmaceutical ingredients (APIs). The method includes subjecting a reaction mixture with an API precursor to solvent extraction to produce a reactant stream with the API precursor. The method includes concentrating the API precursor in the reactant stream using at least one membrane. The method includes carrying out a reaction in a membrane reactor. The method includes separating the API precursor from the reaction stream using a separator. The method includes crystallizing the API precursor using a crystallizer to produce APIs.

An apparatus for capturing carbon dioxide has a membrane separator with a gas inlet, a gas outlet, a channel that extends between the gas inlet and the gas outlet, and pores configured to permit carbon dioxide to pass therethrough, the gas inlet being connected to receive a mixed gas that contains carbon dioxide, wherein carbon dioxide in the mixed gas exits the membrane via the pores, and a remainder of the mixed gas exits the membrane separator via the gas outlet. The pores may be functionalized with nano-particles. A container is filled with an aqueous solution includes a carbon capturing agent and the membrane separator is submerged within the aqueous solution. The carbon capturing agent may be produced by a membrane reactor upstream of the membrane separator. Carbon dioxide exiting the membrane separator via the functional pores reacts with the carbon capturing agent to produce a carbon negative compound.

An electrochlorination system includes an electrolyzer fluidically connectable between a source of feed fluid and a product fluid outlet, and a sub-system configured to one of increase a pH of the feed fluid, or increase a ratio of monovalent to divalent ions in the feed fluid, upstream of the electrolyzer.

A method of separately producing tert-butanol and sec-butanol, comprising the steps of introducing a mixed butenes stream to a tube side of a reaction membrane unit, introducing a TBA reactor water feed to the tube side of the reaction membrane unit, introducing a sweep gas to a shell side of the reaction membrane unit, introducing an SBA reactor water feed to the shell side, allowing the mixed butenes stream to contact the tube side of a such that selective gases in the mixed butenes stream permeate through the membrane to the shell side, allowing the selective gases that permeate through the membrane to react with water to produce sec-butanol, allowing retentate gases that fail to permeate through the membrane to react with water to produce tert-butanol, collecting the tert-butanol in a TBA reactor effluent, and collecting the sec-butanol in a SBA reactor effluent.