The invention is directed to a method for recovering lactose from an aqueous lactose solution comprising a concentration step, wherein water is removed from the aqueous lactose solution by freezing out water at a temperature below the eutectic temperature of the aqueous lactose solution and at a lactose concentration higher than the eutectic concentration of the aqueous lactose solution, thereby obtaining a concentrated lactose solution; and a crystallization step, wherein at least part of the concentrated lactose solution is subjected to crystallization at a temperature above the eutectic temperature of the concentrated lactose solution, thereby obtaining lactose crystals.

The invention relates to a method for recovering an organic compound from a feed stream comprising the steps of extracting the organic compound into an organic solvent, thereby obtaining a mixture of the solvent and the organic compound; and simultaneously crystallizing the solvent and the organic compound by cooling the mixture; and separating the solid organic solvent and solid organic compound.

The invention relates to a method for recovering an organic compound from a feed stream comprising the steps of extracting the organic compound into an organic solvent, thereby obtaining a mixture of the solvent and the organic compound; and simultaneously crystallizing the solvent and the organic compound by cooling the mixture; and separating the solid organic solvent and solid organic compound.

The present invention provides one method for the preparation of pharmaceutically acceptable chlorogenic acid, which comprises the following steps: a. Treating the sample aqueous solution; b. Freezing; c. Thawing and filtering; d. Treating the residue organic phase; e. Concentrating and crystallizing; f. Choosing the number of times to repeat steps a-e according to the variability of chlorogenic acid content in samples; g. Drying. If the chlorogenic acid extract is isolated and purified using this method, water-soluble impurities and liposoluble impurities can be well removed, that allows the impurity content of final products has fulfilled the requirements for medicine; meanwhile, the procedures of this method are simple, and organic solvents can be recycled for further use, with low cost. This method can be applied for the further isolation and purification of chlorogenic acid extract obtained by various ways, especially for the preparation of pharmaceutically acceptable chlorogenic acid.

The present invention provides one method for the preparation of pharmaceutically acceptable chlorogenic acid, which comprises the following steps: a. Treating the sample aqueous solution; b. Freezing; c. Thawing and filtering; d. Treating the residue organic phase; e. Concentrating and crystallizing; f. Choosing the number of times to repeat steps a-e according to the variability of chlorogenic acid content in samples; g. Drying. If the chlorogenic acid extract is isolated and purified using this method, water-soluble impurities and liposoluble impurities can be well removed, that allows the impurity content of final products has fulfilled the requirements for medicine; meanwhile, the procedures of this method are simple, and organic solvents can be recycled for further use, with low cost. This method can be applied for the further isolation and purification of chlorogenic acid extract obtained by various ways, especially for the preparation of pharmaceutically acceptable chlorogenic acid.

Methods of analyzing analytes from a liquid medium are disclosed. A system and apparatus for the analysis of analytes from a liquid medium are further disclosed. In particular, methods and apparatus of analyzing analytes by freezing liquid medium and partitioning the analyte into a sorptive stirrer are disclosed. Further, the methods and apparatus of the present invention can be useful in concentrating and isolating target chemicals of high value.

Methods of analyzing analytes from a liquid medium are disclosed. A system and apparatus for the analysis of analytes from a liquid medium are further disclosed. In particular, methods and apparatus of analyzing analytes by freezing liquid medium and partitioning the analyte into a sorptive stirrer are disclosed. Further, the methods and apparatus of the present invention can be useful in concentrating and isolating target chemicals of high value.

Provided is a production method for a concentrated product, using a freeze-concentration method having a high yield rate (low loss rate) that is practically applicable, as required in large-scale (commercial scale) production. The production method for concentrated product using the freeze-concentration method includes: an ice crystal generation step in which a fluid to be treated is cooled, ice crystals of the fluid are generated in the fluid, and a mixed fluid to be treated is formed wherein the mixed fluid to be treated is comprised of the ice crystals and a concentrated fluid produced from the fluid to be treated by generating the ice crystals in the fluid thereby the fluid is concentrated; and an ice crystal separation step in which the mixed fluid is separated into the concentrated fluid to be treated and the ice crystals, and the separated concentrated fluid be treated is retrieved.

Provided is a production method for a concentrated product, using a freeze-concentration method having a high yield rate (low loss rate) that is practically applicable, as required in large-scale (commercial scale) production. The production method for concentrated product using the freeze-concentration method includes: an ice crystal generation step in which a fluid to be treated is cooled, ice crystals of the fluid are generated in the fluid, and a mixed fluid to be treated is formed wherein the mixed fluid to be treated is comprised of the ice crystals and a concentrated fluid produced from the fluid to be treated by generating the ice crystals in the fluid thereby the fluid is concentrated; and an ice crystal separation step in which the mixed fluid is separated into the concentrated fluid to be treated and the ice crystals, and the separated concentrated fluid be treated is retrieved.

The present invention provides a crystal of reduced glutathione that is stable, and is easy to process, and a method for producing the crystal. According to the present invention, a crystal of a metal salt of reduced glutathione is produced by suspending an amorphous solid of a metal salt of reduced glutathione in a hydrophobic organic solvent, and adding water to the resulting suspension to precipitate a crystal of a metal salt of reduced glutathione.