Mixed rare earth carbonate may be prepared by mixing a rare earth sulfate solution with a precipitating agent comprising a first sodium carbonate (Na.sub.2CO.sub.3) solution, to form a first mixture, and generating a higher sulfate rare earth carbonate wet cake from the first mixture. The higher sulfate rare earth carbonate wet cake can be mixed with a second sodium carbonate (Na.sub.2CO.sub.3) solution to form a second mixture, and a lower sulfate rare earth carbonate can be generated from the second mixture.

A manufacturing apparatus of a precursor for positive electrode active material includes a reactor configured to receive a reaction solution and produce a precursor for positive electrode active material through a co-precipitation reaction of the reaction solution, a filtration unit disposed inside the reactor and configured to discharge a filtrate excluding solids in the reaction solution to the outside of the reactor when the reaction solution reaches a predetermined solution level, an extraction unit configured to extract a portion of the reaction solution when the size of a precursor particle in the reaction solution reaches a predetermined size, and a storage tank configured to receive a reaction solution extracted from the reactor through the extraction unit. A method of manufacturing and the precursor are also provided.

A system and method for generating a water-soluble mixture of oligosaccharides for facile conversion to fermentable sugars is provided. The method describes crushing, grinding, or both, a mixture of a cellulose feedstock and a solid acid catalyst, under pressure to induce a solid-solid interaction between the cellulosic feedstock and the solid acid catalyst to induce a chemical reaction to produce a grinded mixture, wherein the crusher assembly comprises rollers, introducing water to separate the grinded mixture into solids and a solution, wherein the solution comprises the oligosaccharides and enzymatically converting the solution to fermentable sugars.

A method of treatment of plasma with a physiologically compatible spray dry stable acidic substance (SDSAS) prior to or contemporaneously with spray drying of the plasma that results in greater recovery and greater long-term stabilization of the dried plasma proteins as compared to spray dried plasma that has not be subject to the formulation method of the present invention, as well as compositions related to plasma dried by the methods of the present invention.

The present invention generally relates to microfluidic droplets and, in particular, to multiple emulsion microfluidic droplets. In certain aspects, particles such as gel particles can be prepared in an aqueous carrier from aqueous droplets (or a non-aqueous carrier from non-aqueous droplets). For example, in some embodiments, double-emulsion droplets of a first fluid, surrounded by a second fluid, contained in a carrier fluid may be prepared, where the first fluid forms a gel and the second fluid is removed. For instance, the second fluid may be dissolved in the carrier fluid, or the second fluid may be hardened, then removed, for example, due to a change in pH. Other embodiments of the present invention are generally directed to kits containing such microfluidic droplets, microfluidic devices for making such microfluidic droplets, or the like.

The invention relates to a method and an assembly for recovering magnesium ammonium phosphate from slurry supplied to a reaction container (10) in which an aerobic milieu that is alkaline as a result of CO.sub.2-stripping is present and in which the slurry is guided in a circuit with the aid of ventilation. Cationic magnesium, such as magnesium chloride, is added to the slurry, and magnesium ammonium phosphate crystals which are crystallized out of the slurry are removed via a removal device (30) provided in the base region of the reaction container. The slurry is supplied from the first reaction container (10) to a second reaction container (12) via a first line (14), wherein an anaerobic milieu is set in the second reaction container in order to redissolve the phosphate, and MAP crystals crystallized in the second reaction container are supplied to the first reaction container.

A lithium carbonate production device is provided which can efficiently produce lithium carbonate without requiring a large pressure for supplying carbon dioxide gas, by a simple structure. A lithium carbonate production device (1) includes: a sealed reaction tank (2) which stores a lithium hydroxide aqueous solution A; a supply unit (3) for the lithium hydroxide aqueous solution; a carbon dioxide gas supply unit (4); a circulation unit (21) for the lithium hydroxide aqueous solution; and a nozzle which is provided at the head of the circulation unit (21) for the lithium hydroxide aqueous solution, and has a diameter which gradually decreases from a base end side to a head side.

A lithium carbonate production device is provided which can efficiently produce lithium carbonate without requiring a large pressure for supplying carbon dioxide gas, by a simple structure. A lithium carbonate production device (1) includes: a sealed reaction tank (2) which stores a lithium hydroxide aqueous solution A; a supply unit (3) for the lithium hydroxide aqueous solution; a carbon dioxide gas supply unit (4); a circulation unit (21) for the lithium hydroxide aqueous solution; and a nozzle which is provided at the head of the circulation unit (21) for the lithium hydroxide aqueous solution, and has a diameter which gradually decreases from a base end side to a head side.

The present invention pertains to a mordenite zeolite having excellent particle uniformity, and a method for preparing same, the method including a step for providing an aqueous solution in which a silica precursor is dissolved; a step for providing an aqueous solution in which a structure-inducing substance and an alumina precursor are dissolved; a step for providing an aqueous solution in which a surfactant is dissolved; a step for preparing a silica-alumina aqueous solution by mixing and stirring the basic silica suspension and the alumina aqueous solution; a step for preparing a zeolite synthesis composition by adding the surfactant aqueous solution to the silica-alumina aqueous solution; a step for gelling the zeolite synthesis composition; and a step for crystallizing the gelled zeolite synthesis composition.

An apparatus for controlling acid-rock reaction includes a first reactor, a second reactor connected to the first reactor and configured to produce a spent acid through reaction of a rock with an acid aqueous solution and to introduce the spent acid into the first reactor, the first reactor being configured to react a rock disk with the spent acid introduced from the second reactor, a sample extractor connected to the first reactor and configured to extract, from the first reactor, a predetermined amount of the spent acid reacting with the rock disk in the first reactor, and a data acquisition device configured to acquire temperature and pressure data of the first reactor and the second reactor and control the first reactor and the second reactor based on he acquired temperature and pressure data of the first reactor and the second reactor.