Patent classifications
B01D9/0018
Crystallization system with frame elements
A system for crystallizing a material that is dissolved in a solvent includes: a crystallization device through which a solution that is to be concentrated flows, the solution including the solvent containing the material to be crystallized and dissolved in the solvent, and a liquid having a lower temperature than the solution to be concentrated. The system includes at least one flow channel guiding the solution to be concentrated and at least one flow channel guiding the liquid, where the inner space of each respective flow channel guiding the liquid is delimited at least in part by a membrane wall that is permeable for the vaporous solvent, where a vapor pressure difference enables the solvent to pass from the solution to be concentrated across the membrane wall.
Methods for Purification of Non-Psychoactive Isoprenoid Compounds from Biological Extracts
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.
PROCESS FOR PRODUCING HIGH PURITY ALUMINIUM MATERIALS
A process for producing high purity alumina (HPA) or high purity aluminium salts from an aluminium-bearing material, such as is disclosed. An aluminium-bearing solution is first obtained by either dissolving or leaching the aluminium-bearing material. Aluminium is then selectively extracted by liquid-liquid or liquid-solid extraction to obtain an aluminium-enriched liquid or aluminium-enriched solid phase. Minor metal impurities still remaining in the aluminium-enriched liquid or solid phase are removed by scrubbing the aluminium-enriched liquid or aluminium-loaded ion exchange resin with an aqueous solution thereby producing a metal impurity-depleted aluminium-enriched liquid or metal impurity-depleted aluminium enriched solid phase. Aluminium is then stripped from the scrubbed liquid or solid phases with an acidic aqueous solution to produce an aluminium-enriched aqueous solution. High purity aluminium salts may be crystallised from said solution. Alternatively, the pH of said solution may be raised to precipitate an aluminium precipitate, such as Al(OH)3, which is then calcined to produce HPA.
Wastewater treatment equipment and treatment method thereof
A wastewater treatment equipment and a treatment method of a wastewater are provided. The wastewater treatment equipment includes: a microfiltration unit, configured to receive and filter a wastewater to obtain a solution; a membrane salt separation unit, configured to receive the solution and separate monovalent ions and multivalent ions from the solution to obtain a first solution including the monovalent ions and a second solution including the multivalent ions; a first evaporative crystallization unit, configured to crystallize the first solution to form a monovalent salt; and a second evaporative crystallization unit, configured to crystallize the second solution to form a mixed salt; the microfiltration unit is connected to the membrane salt separation unit, and the first evaporative crystallization unit and the second evaporative crystallization unit are both directly connected to the membrane salt separation unit, the wastewater treatment equipment can achieve the standard discharge of wastewater.
METHOD AND APPARATUS FOR REMOVING SULFUR OXIDES FROM GAS
Methods, apparatus, and compositions for cleaning gas. The use of segmented multistage ammonia-based liquid spray with different oxidation potentials to remove sulfur compounds from gas. The use of different oxidation potentials may reduce unwanted ammonia slip.
METHOD FOR THE SEPARATION OF THE ISOPRENIC CONSTITUENTS OF GUAYULE
Method for the separation of at least one isoprenic constituent from the resin of a plant of guayule and/or of the guayule type comprising the steps of: a) providing a defatted resin of guayule and/or of the guayule type; b) subjecting the defatted resin to partitioning of the liquid-liquid type with solvents that are immiscible in each other thus obtaining an apolar extract containing the isoprenic constituents guayulin A, guayulin B and argentatin B; and a polar extract containing the isoprene constituents argentatin A, argentatin C and argentatin D; and c) separating at least one isoprenic constituent from said polar extract and/or from the apolar extract thus obtained, wherein step c) comprises a step in which the polar extract is subjected to partitioning of the liquid-liquid type with solvents immiscible in each other and/or a step in which the apolar extract is subjected to partitioning of the solid-liquid type.
CRYSTALLINE FORM A OF OBETICHOLIC ACID AND PREPARATION METHOD THEREOF
The present invention relates to crystalline Form A of obeticholic acid and the preparation method thereof. The present invention provides Form A having characteristic peaks at 2theta value of 4.90.2, 5.20.2, 9.90.2. The present invention provides a novel crystalline form of obeticholic acid, which has good stability, good processability and other favorable properties, and is suitable for storage and usage as a final product. In addition, the preparation method is simple, low cost, and has great value for the future optimization and development of obeticholic acid.
Saline Water Desalination, Concentration, and Crystallization
This invention obtains fresh water and only solid waste from input saline water. This result is commonly known as desalination having zero liquid discharge (ZLD). The current common means of ZLD desalination is to use any common desalination process such as distillation, reverse osmosis, electrodialysis, etc. followed by brine recovery and crystallization which are both based on evaporation of water processes. This invention provides an alternative to the commonly used brine recovery and crystallization processes to produce only solid waste. This invention has major components of (a) new ion concentration process, (b) combinations of prior art desalination processes and new ion concentration processes to produce fresh water and nearly saturated saline water from a saline water input, (c) another combination of prior art desalination and new ion concentration processes to produce fresh water and supersaturated saline water having a salinity in the metastable state zone from a nearly saturated saline water input, and (d) a separate process that precipitates out solids from the supersaturated saline water after seed crystals are introduced. The process also provides a means that prevents long-term buildup of precipitated solids in the ion concentration process that supersaturates the nearly saturated saline water input. The ion concentration process is composed of variations of prior art ion transfer processes where electrodialysis and capacitive deionization are examples.
NITRIDE STABILIZED CORE/SHELL NANOPARTICLES
Nitride stabilized metal nanoparticles and methods for their manufacture are disclosed. In one embodiment the metal nanoparticles have a continuous and nonporous noble metal shell with a nitride-stabilized non-noble metal core. The nitride-stabilized core provides a stabilizing effect under high oxidizing conditions suppressing the noble metal dissolution during potential cycling.
Process for the separation of long chain amino acids and dibasic acids
There is disclosed a process for the separation of long chain amino acid and long chain dibasic acid, comprising: (1) recovering alkylamine by distilling or by extracting with an extractant solvent; (2) adding an acid an extractant solvent to the aqueous solution of step (1) to form an acidic salt of long chain amino acid to extract long chain dibasic acid; (3) separating the mixture of step (2) into an aqueous phase and an extractant phase; (4) neutralizing the aqueous phase of step (3) with an alkali hydroxide or ammonium hydroxide to obtain a crystalline solid of long chain amino acid; (5) cooling the extractant phase of step (3) to crystallize the long chain dibasic acid and recovering the dibasic acid by solid-liquid separation; and (6) recovering the extractant solvent of step (5) and isolating the alkanoic acid by distillation.