The present invention addresses the problem of providing a method for efficiently producing uniform microparticles of curcumin and/or -oryzanol at a higher yield. The target microparticles are produced by dissolving a starting material in a solvent to give a starting material solution and then subjecting the starting material solution to crystallization by a poor solvent method to thereby deposit the starting material. To prepare the starting material solution, curcumin and/or -oryzanol are used as the starting material(s) and ethanol is used as the solvent. The starting material(s) and the solvent are stirred in a pressurized state at a temperature of 78.3-130 C. inclusive to give the starting material solution. Then, the starting material solution thus obtained is subjected to crystallization by the poor solvent method and thus the target microparticles are produced.

Disclosed herein is a use of an inorganic salt to form and regenerate a draw solute for forward osmosis, wherein the inorganic salt is selected from one or more of the group selected from sodium sulfate, calcium lactate, disodium phosphate, tetrasodium pyrophosphate, and hydrates thereof. Also disclosed herein is a method of forward osmosis using said inorganic salt.

The present invention addresses the problem of providing a method for efficiently producing uniform microparticles of curcumin and/or -oryzanol at a higher yield. The target microparticles are produced by dissolving a starting material in a solvent to give a starting material solution and then subjecting the starting material solution to crystallization by a poor solvent method to thereby deposit the starting material. To prepare the starting material solution, curcumin and/or -oryzanol are used as the starting material(s) and ethanol is used as the solvent. The starting material(s) and the solvent are stirred in a pressurized state at a temperature of 78.3-130 C. inclusive to give the starting material solution. Then, the starting material solution thus obtained is subjected to crystallization by the poor solvent method and thus the target microparticles are produced.

The invention relates to a process of creating particles of controlled size by creating them in the interstitial regions in a batch, semi-continuous, or continuous liquid phase. The method comprises making solid particles comprising: adding a precursor material to a liquid carrier to form a liquid continuous phase, wherein the concentration of the precursor material is from about 5% to about 99% by weight of the continuous liquid phase; adding an inert phase into the liquid continuous phase of step a, resulting in an inert phase and continuous liquid phase mixture having a volume fraction of the inert phase of from about 30% to about 98% and inert phase domain size of about 0.2 to about 200 m; transforming the precursor material physically or chemically, resulting in the formation of solid particles.

The present invention relates to 2-isopropoxy-5-methyl-4-(piperidin-4-yl) aniline dihydrochloride monohydrate and a preparation method of the same. The 2-isopropoxy-5-methyl-4-(piperidin-4-yl) aniline dihydrochloride monohydrate has a very good crystal form and is well suitable for recrystallization purification; further, the effect of impurity removal effect is very good, and any single impurity can be controlled less than 0.1%.

It discloses a new industrial crystallization method of Cefuroxime Sodium, wherein supercritical fluid extraction technology and traditional crystalline technology are combined to realize the recrystallization of Cefuroxime Sodium. Processes such as extraction, adsorption, crystallization and drying are carried out with a supercritical fluid, a solvent, an extraction cell and a crystallization tank to realize the recrystallization of Cefuroxime Sodium under a specific pressure at a specific temperature.

A purification apparatus and a purification method using the purification apparatus. A solution stored in a solution storage tank is diffused/agitated with an ultrasonic wave. An air compressor transfers the solution to a reactor. The solution is mixed in the reactor with a solvent fed through another passage to produce a reactant.

The present invention relates to 2-isopropoxy-5-methyl-4-(piperidin-4-yl) aniline dihydrochloride monohydrate and a preparation method of the same. The 2-isopropoxy-5-methyl-4-(piperidin-4-yl) aniline dihydrochloride monohydrate has a very good crystal form and is well suitable for recrystallization purification; further, the effect of impurity removal effect is very good, and any single impurity can be controlled less than 0.1%.

Disclosed herein is a use of an inorganic salt to form and regenerate a draw solute for forward osmosis, wherein the inorganic salt is selected from one or more of the group selected from sodium sulfate, calcium lactate, disodium phosphate, tetrasodium pyrophosphate, and hydrates thereof. Also disclosed herein is a method of forward osmosis using said inorganic salt.

Compositions and methods used in the modification of crystallization of aluminum hydroxide from liquor in an aluminum hydroxide production process, such as the Bayer process. More particularly, crystal growth modifier compositions comprising a component of crude corn oil derived from a bioethanol production process and/or a component of biodiesel and methods of using such compositions to modify particle size and distribution of precipitated alumina trihydrate in a precipitation liquor crystallization process.