A system and method for preparing a vanadium battery high-purity electrolyte, comprising preparing a low-valence vanadium oxide with a valence of 3.5 with liquid phase hydrolysis and fluidization reduction with vanadium oxytrichloride, adding clean water and sulfuric acid for dissolution, and further performing ultraviolet activation to obtain the vanadium electrolyte, for use in an all-vanadium redox flow battery stack. The high-temperature tail gas in the reduction fluidized bed is combusted for preheating the vanadium powder material, to recover the sensible heat and latent heat of the high-temperature tail gas, and the sensible heat of the reduction product is recovered through heat transfer between the reduction product and the fluidized nitrogen gas. An internal member is arranged in the reduction fluidized bed to realize the precise regulation of the valence state of the reduction product, and ultraviolet is used to activate the vanadium ions, improving the activity of the electrolyte.

Systems and methods of producing potassium sulfate can involve converting a mixed salts feed stream into a conversion end slurry in a conversion unit, the mixed salts feed comprising at least one potassium-containing salt, at least one chloride-containing salt, at least one magnesium-containing salt and at least one sulfate-containing salt and the conversion end slurry comprising schoenite; separating conversion end slurry into a conversion end solids stream and a conversion brine; leaching the conversion end solids stream in a crystallization unit to produce a potassium sulfate product stream comprising potassium sulfate and a crystallizer mother liquor comprising magnesium sulfate and potassium sulfate; collecting heat generated in the conversion unit by a heat pump; and providing at least a portion of the heat collected to the crystallization unit to regulate a temperature of the potassium sulfate product stream and the crystallizer mother liquor stream contained in the crystallization unit.

Systems and methods of producing potassium sulfate can involve converting a mixed salts feed stream into a conversion end slurry in a conversion unit, the mixed salts feed comprising at least one potassium-containing salt, at least one chloride-containing salt, at least one magnesium-containing salt and at least one sulfate-containing salt and the conversion end slurry comprising schoenite; separating conversion end slurry into a conversion end solids stream and a conversion brine; leaching the conversion end solids stream in a crystallization unit to produce a potassium sulfate product stream comprising potassium sulfate and a crystallizer mother liquor comprising magnesium sulfate and potassium sulfate; collecting heat generated in the conversion unit by a heat pump; and providing at least a portion of the heat collected to the crystallization unit to regulate a temperature of the potassium sulfate product stream and the crystallizer mother liquor stream contained in the crystallization unit.

A chlorine dioxide solution generating apparatus is provided for use primarily in water treatment. The apparatus has a reaction chamber supplied with metered quantities of an acidic solution and a chlorite or chlorate solution whereby a reservoir of a chlorine dioxide solution is generated and retained within the reaction chamber. A conduit is provided along which a pressurized flow of a motive fluid is fed and with which the interior of the reaction chamber communicates via a dip tube. A venturi is located in the conduit adjacent an outlet from the dip tube whereby suction is applied to the reaction chamber by the pressurized flow of motive fluid. The suction draws chlorine dioxide solution from the reservoir whereby it is entrained into the flow of motive fluid. A controller is provided to control flow of motive fluid and metering of the supply of the solutions to the reaction chamber.

A chlorine dioxide solution generating apparatus is provided for use primarily in water treatment. The apparatus has a reaction chamber supplied with metered quantities of an acidic solution and a chlorite or chlorate solution whereby a reservoir of a chlorine dioxide solution is generated and retained within the reaction chamber. A conduit is provided along which a pressurized flow of a motive fluid is fed and with which the interior of the reaction chamber communicates via a dip tube. A venturi is located in the conduit adjacent an outlet from the dip tube whereby suction is applied to the reaction chamber by the pressurized flow of motive fluid. The suction draws chlorine dioxide solution from the reservoir whereby it is entrained into the flow of motive fluid. A controller is provided to control flow of motive fluid and metering of the supply of the solutions to the reaction chamber.

The present invention provides a method for manufacturing a polymer by a flow-type reaction.

The method includes introducing a liquid A of an anionic polymerizable monomer, a liquid B of an anionic polymerization initiator, and a polymerization terminator into different flow paths, allowing the liquids to flow in the flow paths, allowing the liquid A and the liquid B to join together, subjecting the monomer to anionic polymerization while the liquids having joined together are flowing to downstream in a reaction flow path, and allowing a solution, which is obtained by the polymerization reaction and flows in the reaction flow path, and the polymerization terminator to join together so as to terminate the polymerization reaction and to obtain a polymer having a number-average molecular weight of 5,000 to 200,000.

A static mixer is disposed in the reaction flow path, and a polymer having a number-average molecular weight equal to or greater than 2,000 is introduced into an inlet port of the mixer. The present invention also provides a flow-type reaction system suitable for performing the manufacturing method.

Techniques are provided for catalyst preparation. A system for catalyst preparation may include an agitator disposed inside a polymerization catalyst tank and configured to mix a polymerization catalyst and a solvent to generate a polymerization catalyst solution. The system may also include a heating system coupled to the polymerization catalyst tank and configured to maintain a temperature of the polymerization catalyst solution above a threshold. The system may also include a precontactor configured to receive feed streams comprising an activator and the polymerization catalyst solution from the polymerization catalyst tank to generate a catalyst complex. The system may also include a transfer line configured to transfer the catalyst complex from an outlet of the precontactor to a reactor.

Techniques are provided for catalyst preparation. A system for catalyst preparation may include an agitator disposed inside a polymerization catalyst tank and configured to mix a polymerization catalyst and a solvent to generate a polymerization catalyst solution. The system may also include a heating system coupled to the polymerization catalyst tank and configured to maintain a temperature of the polymerization catalyst solution above a threshold. The system may also include a precontactor configured to receive feed streams comprising an activator and the polymerization catalyst solution from the polymerization catalyst tank to generate a catalyst complex. The system may also include a transfer line configured to transfer the catalyst complex from an outlet of the precontactor to a reactor.

Methods and systems for temperature-controlled, on-site generation of peracids, namely peroxycarboxylic acids and peroxycarboxylic acid forming compositions are disclosed. In particular, methods for using an adjustable biocide formulator or generator system overcome the limitations of temperature on the kinetics of the peracid generation and/or peracid decomposition inside an adjustable biocide formulator or generator system. The methods include the controlling of the temperature of at least one raw starting material, namely water, to improve upon methods of on-site generation of peracids. The methods allow for the generation of user-selected chemistry without regard to the ambient temperatures of the raw starting materials and/or the biocide formulator or generator system.

Methods and systems for temperature-controlled, on-site generation of peracids, namely peroxycarboxylic acids and peroxycarboxylic acid forming compositions are disclosed. In particular, methods for using an adjustable biocide formulator or generator system overcome the limitations of temperature on the kinetics of the peracid generation and/or peracid decomposition inside an adjustable biocide formulator or generator system. The methods include the controlling of the temperature of at least one raw starting material, namely water, to improve upon methods of on-site generation of peracids. The methods allow for the generation of user-selected chemistry without regard to the ambient temperatures of the raw starting materials and/or the biocide formulator or generator system.