A preparation method of inverse opal material for visible-light-driven photocatalytic degradation of organic pollutants includes 1) using titanium dioxide precursor as raw material, preparing nitrogen-doped titanium dioxide inverse opal by one-step process in the presence of nitrogen source, and 2) in the presence of reducing agent, using the nitrogen-doped titanium dioxide inverse opal, selenium precursor, and cadmium precursor as raw materials to prepare the cadmium selenide sensitized nitrogen-doped titanium dioxide inverse opal.

A method for forming, or crystallising, clathrates hydrates of a host molecule in a liquid including water includes the following consecutive steps: cooling the liquid to a temperature no higher than the crystallisation temperature of the clathrates hydrates; and placing the cooled liquid in contact with host molecules that are capable of forming clathrates hydrates and are adsorbed on a solid support that has a large specific surface area and is made of a hydrophobic and apolar material, whereby the host molecules are desorbed from the solid support that has a large specific surface area and is made of a hydrophobic and apolar material, and react with the water of the liquid in order to provide a liquid containing clathrates hydrates and the solid support.

A method for forming, or crystallising, clathrates hydrates of a host molecule in a liquid including water includes the following consecutive steps: cooling the liquid to a temperature no higher than the crystallisation temperature of the clathrates hydrates; and placing the cooled liquid in contact with host molecules that are capable of forming clathrates hydrates and are adsorbed on a solid support that has a large specific surface area and is made of a hydrophobic and apolar material, whereby the host molecules are desorbed from the solid support that has a large specific surface area and is made of a hydrophobic and apolar material, and react with the water of the liquid in order to provide a liquid containing clathrates hydrates and the solid support.

The present invention relates to processes for preparing 6-(4-bromo-2-fluorophenylamino)-7-fluoro-3-methyl-3H-benzoimidazole-5-carboxylic acid (2-hydroxyethyoxy)-amide, processes for preparing crystallized 6-(4-bromo-2-fluorophenylamino)-7-fluoro-3-methyl-3H-benzoimidazole-5-carboxylic acid (2-hydroxyethyoxy)-amide, and intermediates useful therefore. Also provided herein are pharmaceutical compositions comprising this crystallized compound.

The present invention relates to processes for preparing 6-(4-bromo-2-fluorophenylamino)-7-fluoro-3-methyl-3H-benzoimidazole-5-carboxylic acid (2-hydroxyethyoxy)-amide, processes for preparing crystallized 6-(4-bromo-2-fluorophenylamino)-7-fluoro-3-methyl-3H-benzoimidazole-5-carboxylic acid (2-hydroxyethyoxy)-amide, and intermediates useful therefore. Also provided herein are pharmaceutical compositions comprising this crystallized compound.

Monodisperse particles having: a single pure crystalline phase of a rare earth-containing lattice, a uniform three-dimensional size, and a uniform polyhedral morphology are disclosed. Due to their uniform size and shape, the monodisperse particles self assemble into superlattices. The particles may be luminescent particles such as down-converting phosphor particles and up-converting phosphors. The monodisperse particles of the invention have a rare earth-containing lattice which in one embodiment may be an yttrium-containing lattice or in another may be a lanthanide-containing lattice. The monodisperse particles may have different optical properties based on their composition, their size, and/or their morphology (or shape). Also disclosed is a combination of at least two types of monodisperse particles, where each type is a plurality of monodisperse particles having a single pure crystalline phase of a rare earth-containing lattice, a uniform three-dimensional size, and a uniform polyhedral morphology; and where the types of monodisperse particles differ from one another by composition, by size, or by morphology. In a preferred embodiment, the types of monodisperse particles have the same composition but different morphologies. Methods of making and methods of using the monodisperse particles are disclosed.

Monodisperse particles having: a single pure crystalline phase of a rare earth-containing lattice, a uniform three-dimensional size, and a uniform polyhedral morphology are disclosed. Due to their uniform size and shape, the monodisperse particles self assemble into superlattices. The particles may be luminescent particles such as down-converting phosphor particles and up-converting phosphors. The monodisperse particles of the invention have a rare earth-containing lattice which in one embodiment may be an yttrium-containing lattice or in another may be a lanthanide-containing lattice. The monodisperse particles may have different optical properties based on their composition, their size, and/or their morphology (or shape). Also disclosed is a combination of at least two types of monodisperse particles, where each type is a plurality of monodisperse particles having a single pure crystalline phase of a rare earth-containing lattice, a uniform three-dimensional size, and a uniform polyhedral morphology; and where the types of monodisperse particles differ from one another by composition, by size, or by morphology. In a preferred embodiment, the types of monodisperse particles have the same composition but different morphologies. Methods of making and methods of using the monodisperse particles are disclosed.

High-purity hydrous D-allose crystals and a method of efficiently obtaining the crystals are provided. To a D-allose-containing solution having a purity of D-allose of at least 80% (g/g) in a solute, in a metastable region in a supersaturated state of 30 C. or less, D-allose seed crystals are added. Then, the temperature of the solution is lowered by 10 C. or more for cooling and crystallization to initially obtain hydrous D-allose crystals, and the crystallization water thereof is removed in a specified temperature zone to obtain novel anhydrous D-allose crystals.

Quantum dots and methods of making quantum dots are provided.

Quantum dots and methods of making quantum dots are provided.