Patent classifications
B01D15/362
METHOD FOR PRODUCING PSICOSE
The present invention relates to a method for effectively utilizing fructose raffinate obtained in the process for separating psicose conversion product with a high purity chromatography in the process for preparing psicose, and more specifically, it is utilized for preparation of fructose-containing raw material solution for preparing psicose by supplying the fructose raffinate obtained in the separation step of psicose preparation into the psicose conversion reaction.
Process for removing strontium ions from bodily fluids using metallate ion exchange compositions
A process for removing Sr.sup.2+ toxins from bodily fluids is disclosed. The process involves contacting the bodily fluid with an ion exchanger to remove the metal toxins in the bodily fluid, including blood and gastrointestinal fluid. Alternatively, blood can be contacted with a dialysis solution which is then contacted with the ion exchanger. The ion exchangers are represented by the following empirical formula:
A.sub.mZr.sub.aTi.sub.bSn.sub.cM.sub.dSi.sub.xO.sub.y. A composition comprising the above ion exchange compositions in combination with bodily fluids or dialysis solution is also disclosed. The ion exchange compositions may be supported by porous networks of biocompatible polymers such as carbohydrates or proteins.
Method for producing lithium hydroxide monohydrate from brines
A method for LiOHH.sub.2O production from lithium-bearing multicomponent hydromineral raw materials includes filtering lithium-bearing brine contaminated with suspended particles with regeneration of filters and processing of used regenerate, and obtaining pregnant lithium-bearing brine, isolation of lithium chloride from the brine in the form of a primary concentrate in sorption-desorption modules, and nanofiltration of the primary lithium concentrate from magnesium, calcium and sulfate ions. By means of reverse osmosis, electrodialysis concentration and ion-exchange purification from impurities followed by thermal concentration, the primary lithium concentrate is converted into a pregnant lithium chloride concentrate which is converted into a LiOH solution by membrane electrolysis. The LiOH solution is boiled down, resulting in LiOH.H.sub.2O crystallization.
Mixed-mode chromatography membranes
Described are composite materials and methods of using them for mixed-mode chromatography. In certain embodiments, the composite material comprises a support member, comprising a plurality of pores extending through the support member; and a multi-functional cross-linked gel. The multi-functional cross-linked gel possesses at least two of the following functions or characteristics: cationic, anionic, hydrophobic, hydrophilic, thiophilic, hydrogen bond donating, hydrogen bond accepting, pi-pi bond donating, pi-pi bond accepting, or metal chelating. The composite materials may be used in the separation or purification of a biological molecule or biological ion.
Method for separation and purification of n-acetylglucosamine
The disclosure relates to a method for separation and purification of N-acetyl-glucosamine, and belongs to the technical field of biological engineering. In the disclosure, a raw material solution containing N-acetyl-glucosamine is obtained by microbial fermentation or by hydrolyzing the chitin. The raw material solution is subjected to flocculation pretreatment, and continuous centrifugation or pressure filtration is performed to remove suspended solids such as microorganisms, proteins and polysaccharides to obtain clear liquid. Double-stage ion exchange chromatography is performed to remove impurities such as charged organic molecules and inorganic salts. Membrane concentration is performed to efficiently remove water to improve the concentration of the target product. Spray drying or further evaporation concentration and crystallization are performed. Finally drying is performed to obtain an N-acetyl-glucosamine crystal of which the purity is more than 99%.
CHROMATOGRAPHIC SEPARATION OF SACCHARIDES USING WHOLE CRACKED BEADS OF GEL-TYPE STRONG ACID EXCHANGE RESIN
A method for chromatographically separating a first saccharide from a liquid eluent comprising the first saccharide and a second saccharide by passing the liquid eluent through a bed comprising a gel-type strong acid cation exchange resin in calcium form, wherein the resin is provided in bead form and is characterized by comprising at least 20% whole cracked beads.
CHROMATOGRAPHIC SEPARATION OF SACCHARIDES USING STRONG ACID EXCHANGE RESIN INCORPORATING PRECIPITATED BARIUM SULFATE
A method for chromatographically separating a first saccharide from a liquid eluent comprising the first saccharide and a second saccharide by passing the liquid eluent through a bed comprising a gel-type strong acid cation exchange resin in calcium form, wherein precipitated barium sulfate is incorporated within the resin.
SEPARATION OF OLIGOSACCHARIDES FROM FERMENTATION BROTH
The present invention relates to the isolation and purification of sialylated oligosaccharides from an aqueous medium in which they are produced.
Method for preparing natural L-cysteine crystals by continuous chromatography
The present disclosure relates to a method for preparing L-cysteine crystals, and L-cysteine crystals prepared by the method. Through the method for preparing L-cysteine crystals of the present disclosure, L-cysteine crystals can be obtained from a natural L-cysteine fermentation broth with a high recovery rate and/or purity without a chemical reaction or the use of an artificial synthetic compound.
MODULATION OF CHARGE VARIANTS IN A MONOCLONAL ANTIBODY COMPOSITION
Combinations of different chromatography modalities with particularly refined conditions significantly reduce acid charge variants in a preparation of monoclonal antibodies. The process for reducing acid charge variants utilizes a combination of anion exchange and hydrophobic interaction chromatography, followed by cation exchange chromatography polishing, whereby the levels of acidic or basic charge species of the monoclonal antibodies may be modulated to a desired level.