B01D9/005

TETRAAZADODECANE BASED CHELATING AGENTS FOR SEPARATION OF RARE EARTH ELEMENTS AND METHOD THEREFOR
20230356105 · 2023-11-09 ·

The present invention related to the use of compounds of general formula (I) for separations of rare earth elements (lanthanides) by precipitation, wherein R is selected from the group consisting of H; —CH2COOH; R.sup.2, R.sup.3, R.sup.4, R.sup.5 and R.sup.6 areindependently selected from the group consisting of H; OH; —NO2; —COOH; phenyl; and/or R.sup.2 and R.sup.3 or R.sup.3 and R.sup.4 or R.sup.4 and R.sup.5 or R.sup.5 and R.sup.6 The invention further relates to a method of separation of rare earth elements by precipitation. together with two neighbouring carbon atoms of the aromatic ring form a six-membered aromatic ring.

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CRYSTALLIZATION SYSTEM AND METHOD USING THERMAL TREATMENT
20230356104 · 2023-11-09 ·

A method of crystallizing a solution (24) having at least one compound mixed (18) with a dissolving agent (20) is provided. The method includes performing a heating process by heating the solution (24) until a current temperature of the solution is equal to a predetermined treatment temperature, maintaining the current temperature at the predetermined treatment temperature for a predetermined treatment time period, performing a cooling process by cooling the solution (24) until the current temperature is less than the predetermined treatment temperature and a crystallization temperature of the at least one compound (18), causing formation of a plurality of crystal particles (30) of the at least one compound by cooling the solution until the current temperature is equal to a predetermined termination temperature of the at least one compound (18), and varying a particle size of each of the crystal particles (30) based on a cooling speed of the solution.

FILTERING AND CONCENTRATING APPARATUS HAVING STIRRING FUNCTION FOR SMALL TERNARY PRECURSOR PARTICLES, AND CONCENTRATING METHOD
20220212121 · 2022-07-07 ·

A filtering and concentrating apparatus having a stirring function for small ternary precursor particles, comprising a barrel (100). One end of the barrel (100) is provided with a first closure (101), and the other end of the barrel (100) is provided with a second closure (102). The barrel (100) or the first closure (101) or the second closure (102) is provided with a feed port (103). One or more discharge pipes (200) are provided on the inner wall of the barrel (100). Microporous filtering mediums (300) communicated with the interior of the discharge pipe (200) are provided on the discharge pipe (200). An end portion of the discharge pipe (200) is communicated with the exterior of the barrel (100). A stirring means (800) is provided inside the barrel (100).

Co-current co-precipitation method of CoNiO.SUB.2 .thermistor powders

The disclosure relates to a co-current co-precipitation method of CoNiO.sub.2 thermistor powders. The method comprises the steps of mixing, stirring, precipitating, aging, suction filtration, washing and drying firstly using nickel nitrate and cobalt nitrate as raw materials to obtain cobalt hydroxide, and then calcining in a tubular furnace at an inert atmosphere to prepare CoNiO.sub.2 nano powders. The method has the advantages of simple operation, low cost, short cycle, high yield and no environmental pollution, and further oxidization of the CoNiO.sub.2 nano material into NiCo.sub.2O.sub.4 thermistor powders can be effectively avoided through selection and adjustment of calcination process parameters and inert atmosphere. A high-precision, fast-response and small-volume temperature sensor material can be prepared from CoNiO.sub.2 thermistor powders obtained by the method of the disclosure.

PURIFICATION OF TRIACYLGLYCERIDE OILS BY AUXILIARY WASHING

The present invention provides an improved method for purification of a primary triacylglyceride oil comprising the steps of washing the primary triacylglyceride oil, trapping assisted removal of chlorinated precursors of MCPDEs by admixing the primary triacylglyceride oil with an auxiliary trapping agent; crystallising the auxiliary trapping agent or the primary triacylglyceride oil; and separating solid and liquid phases of the product.

Diamond pressure apparatus for crystallizing cannabinoids
11285402 · 2022-03-29 ·

An apparatus for purifying diamond CBD oil crystals. A cylindrical glass or metal vessel is provided and supported by least one support post, the vessel having an upper portion and a lower surface having laser etched nucleation sites for initiating crystal growth. A removable head is engageable with the upper portion of the vessel, the head having an uppermost portion and a plurality of ports extending therethrough. A pressurized nitrogen tank is operatively connected to a port of the head, as is a pressure gauge. A safety valve is disposed at the uppermost portion of the head. Optionally, an inline desiccant chamber is also operatively connected to the head. The apparatus crystalizes cannabinoids in either a solventless process or a solvent process.

METHOD AND SYSTEM FOR REFINING LONG CHAIN DICARBOXYLIC ACID

The present disclosure provides a system for refining long chain dicarboxylic acid, comprising: a first membrane filtration unit, for a first membrane filtration of a long chain dicarboxylic acid fermentation broth or a treated liquid therefrom; a first decolorization unit, for carrying out a first decolorization treatment to the filtrate obtained after the membrane filtration; a first acidification/crystallization unit, for carrying out a first acidification/crystallization of a filtrate obtained after the membrane filtration to give a solid-liquid mixture; a first separation unit, for a solid-liquid separation of the solid-liquid mixture; a drying unit, for drying the solid separated by the separation unit to give a first solid. By using the refining system according to the present disclosure, the purity of the obtained product is high, and the disadvantages such as poor quality of the product obtained by crystallization from a solvent and environment pollution caused by a solvent can be overcome.

Ultrasound crystallization device and an ultrasound crystallization system

An ultrasound crystallization device includes a tubular crystallization reactor (102) for conducting process fluid containing substance to be crystallized, an ultrasound source (104) for radiating ultrasound to the tubular crystallization reactor, and a temperature-control structure (105) for controlling the temperature of the process fluid with the aid of temperature-control fluid. The tubular crystallization reactor is shaped to conduct the process fluid to flow around the ultrasound source, and the temperature-control structure comprises a flow-guide structure (106) for guiding at least a part of the temperature-control fluid to flow around the ultrasound source. The flow-guide structure improves the accuracy of the temperature control of the process fluid and also the ability of the temperature control to react to changes.

FORMATION OF STABLE SUBMICRON PEPTIDE OR PROTEIN PARTICLES BY THIN FILM FREEZING

The present invention includes compositions and methods for preparing micron-sized or submicron-sized particles by dissolving a water soluble effective ingredient in one or more solvents; spraying or dripping droplets solvent such that the effective ingredient is exposed to a vapor-liquid interface of less than 50, 100, 150, 200, 250, 200, 400 or 500 cm.sup.−1 area/volume to, e.g., increase protein stability; and contacting the droplet with a freezing surface that has a temperature differential of at least 30° C. between the droplet and the surface, wherein the surface freezes the droplet into a thin film with a thickness of less than 500 micrometers and a surface area to volume between 25 to 500 cm.sup.−1.

Protein crystallization method and crystallization device

Provided are: an economically superior protein crystallization method capable of efficiently finding conditions for crystallization by using a small amount of protein; and a crystallization device used for the method. According to the present invention, a transparent sealed container 1 is filled with a solution of protein, a part of the transparent sealed container 1 being formed of a semipermeable membrane 2 with a molecular weight cut-off that inhibits passage of the protein while allowing passage of a precipitant, and then, a precipitant solution with changed concentration and/or pH of the precipitant is continuously supplied to the semipermeable membrane 2, to crystallize the protein with the precipitant that infiltrates from the semipermeable membrane 2 into the sealed container 1.