B01D9/0059

CHEMICAL REACTION DEVICE AND PARTICLE PRODUCTION METHOD USING CHEMICAL REACTION DEVICE

A chemical reaction device that supplies a raw material liquid into a solution and causes particles to precipitate in the solution is provided. The chemical reaction device includes an agitation tank configured to accommodate the solution, an impeller configured to agitate the solution, and a plurality of discharge parts configured to discharge the raw material liquid into the solution.

WASH COLUMN APPARATUS WITH A STATIC GRID ELEMENT FOR THE USE IN A SUSPENSION CRYSTALLIZATION PROCESS
20190201808 · 2019-07-04 ·

A wash column apparatus for the use in a suspension crystallization process for separating crystals from a crystal suspension mixture includes a cylindrical vessel including a piston with a piston head including a filter and a piston rod, movable in the cylindrical vessel, an inlet for supplying a crystal suspension mixture into the cylindrical vessel, an outlet for discharging mother liquor from the cylindrical vessel, an outlet for discharging crystals or crystal melt from the cylindrical vessel, a circulation conduit for circulating melt arranged outside the vessel, in communication with the wash chamber, a static grid element arranged in the wash chamber for restricting movement of the crystal bed and for directing the wash liquid entering into the cylindrical vessel from the circulation conduit so as to homogeneously distribute it over the entire cross-section of the wash column.

TREATMENT OF WATER
20190194043 · 2019-06-27 ·

A process to treat water includes adding a salt-forming base to the water thereby producing saline water, or thereby forming a salt in the water which is different from a salt that the water started out with, if the water started out as saline. The saline water is treated, at a temperature T1 which is above the saturation temperature of the saline water, in a first membrane separation stage to provide clean water and a first brine, the salinity of the first brine being higher than the salinity of the saline water. The first brine is cooled to a temperature T2 to precipitate some of the salt from the first brine and the precipitated salt is separated from the first brine producing a second brine, the temperature T2 being below the temperature T1 but above the freezing temperature of the first brine. The second brine is treated at a temperature T3 above the saturation temperature of the second brine in a second membrane separation stage to provide clean water and a third brine. The salt-forming base, the temperature T1 and the temperature T2 are selected so that the salt which is formed in the saline water has a solubility in water at the temperature T1 which is at least 1.5 times the solubility of the salt in water at the temperature T2.

Process for the separation of long chain amino acids and dibasic acids
10329240 · 2019-06-25 · ·

There is disclosed a process for the separation of long chain amino acid and long chain dibasic acid, comprising: (1) recovering alkylamine from an aqueous solution of an alkali hydroxide hydrolysis of the mixed amide derivatives by distilling or by extracting with an extractant solvent; (2) cooling the aqueous solution of step (1) to precipitate a mixed alkali salts of long chain amino acid and dibasic acid; (3) recovering the mixed alkali salts of long chain amino acid and dibasic acid to provide a mother liquor; (4) separating long chain amino acid and dibasic acid by acidification-extraction of long chain dibasic acid with an extractant solvent or by selective dissolution of alkali salt of long chain amino acid in an aqueous solvent; and (4) adding an acid to the mother liquor of step (3) to obtain alkanoic acid.

Process for the separation of long chain amino acids and dibasic acids
10329241 · 2019-06-25 · ·

There is disclosed a process for the separation of long chain amino acid and long chain dibasic acid, comprising: (1) cooling the hydrolysis solution to crystallize and separate alkali salt of long chain dibasic acid to provide an aqueous solvent solution; (2) distilling the aqueous solvent solution of step (1) to recover the solvent and to recover alkylamine; (3) cooling the residual solution of step (2) to precipitate and separate alkali salt of long chain amino acid to provide a mother liquor; (4) adding an acid to the mother liquor of step (3) to yield alkanoic acid; (5) adding an acid to an aqueous solution of the alkali salt of long chain dibasic acid of step (1) to obtain long chain dibasic acid; and (6) neutralizing the alkali salt of long chain amino acid of step (3) with an acid to obtain long chain amino acid.

METHOD FOR RECOVERING TITANIUM (HALO) ALKOXIDE FROM A WASTE LIQUID
20190184306 · 2019-06-20 ·

A method for separating one or more titanium (halo) alkoxides from a liquid mixture comprising titanium tetrachloride TiCl.sub.4 and at least one titanium (halo) alkoxide, said method comprising: agitating and cooling the liquid mixture until crystallization of at least one titanium (halo) alkoxide occurs in the liquid mixture; separating the crystallized titanium (halo) alkoxide from the mixture; and optionally, washing the separated, crystallized titanium (halo) alkoxide with a solvent.

Methods for purification of non-psychoactive isoprenoid compounds from biological extracts
10323014 · 2019-06-18 ·

A method for the extraction and isolation of the terpene and isoprenoid compounds from plant material, followed by a centrifugal force induced selective crystallization of isoprenoids resulting in a separation of terpene and isoprenoid fractions. This this method is suitable for the extraction of cannabinoids from Cannabis and the enrichment tetrahydrocannabinolic acid and reduction of tetrahydrocannabinol in an extract. The purity of tetrahydrocannabinolic acid resulting from centrifugal crystallization is such that dissolution and selective recrystallization of tetrahydrocannabinolic acid is possible resulting in >99.9% pure tetrahydrocannabinolic acid, w/w.

Crystal purification in a glass or metal container
10308626 · 2019-06-04 ·

A method for purifying crystals in a glass or metal container. A hydrocarbon is introduced into feed material containing tetrahydrocannabinol (THC). The feed material and hydrocarbon is placed in a glass or metal container. The hydrocarbon is then removed within a few minutes after introduction, leaving at least some hydrocarbon in the feed material. Pressure is allowed to build within the container in an oven or in a jacketed vessel for 2-3 weeks. During this time, THC acid crystals precipitate out and fall to the bottom of the container. The contents of the container are poured into a Buchner funnel and a vacuum is applied thereto in order to pull terpenes into a beaker. The terpenes are placed into an oven in order to purge off any remaining solvent. The funnel is then scraped to acquire THC acid crystals.

DEMILITARIZATION AND DISPOSAL OF HC SMOKE ORDINANCE
20190160391 · 2019-05-30 ·

Demilitarization and disposal of HC smoke ordnance with recovery of constituents thereof as commodities entails mechanically removing from the ordnance a filler comprising hexachloroethane, zinc oxide and grained aluminum; heating the filler to a temperature above the sublimation temperature of hexachloroethane but safely below the temperature at which hexachloroethane chemically decomposes, and draining and collecting the dense hexachloroethane vapor; and conventionally separating the aluminum from the zinc oxide. Filler is supplied to and removed from a heating compartment from above; hexachloroethane drains via a lower portion of the heating compartment.

METHOD FOR PRODUCING PEPTONES COMPRISING PROTEINS AND AMINO ACIDS FROM MUCOUS MEMBRANES OF ANIMALS TO BE SLAUGHTERED, AND THE PEPTONES THEMSELVES
20240199690 · 2024-06-20 ·

A method having the following steps: (1) providing a composition containing proteins and amino acids from mucous membranes of animals for slaughter, inorganic salts and water, wherein the sum of the mass of proteins and amino acids in the dry mass of said composition is 30 to 70 weight percent and the mass of inorganic salts in the dry mass of said composition is at least 7.5 weight percent; (2) filtering the composition to obtain a filtrate and a filter cake; (3) cooling the filtrate to a temperature in the range of 15? C. to 15? C. to form a precipitate; (4) separating the resulting precipitate to obtain the liquid phase as product. The disclosure further relates to the products of this method.