The present invention provides a functional material, its preparation method, touch structures and touch display devices, which can solve the pollution problem in current touch display devices. The functional material includes an inorganic mixed powder with a modified layer, the inorganic mixed powder comprising boron oxide, sodium oxide, lithium oxide, zirconium oxide, aluminum oxide, zinc oxide, titanium oxide, silicon dioxide, calcium oxide, silver complexes, silver phosphate, silver nitrate, tourmaline, silver thiosulfate, carbon nanotubes, aluminum sulfate, manganese, manganese oxide, iron, iron oxide, cobalt, cobalt oxide, nickel, nickel oxide, chromium, chromium oxide, copper, copper oxide, magnesium oxide, boron carbide, silicon carbide, titanium carbide, zirconium carbide, tantalum carbide, molybdenum carbide, boron nitride, chromium nitride, titanium nitride, zirconium nitride, aluminum nitride, chromium boride, Cr.sub.3B.sub.4, titanium boride, zirconium boride, tungsten disilicide, and titanium disilicide; the modified layer being generated by the reaction of a dianhydride and a diamine.

A solid composite material combining: an inorganic pigment in the form of discrete particles each comprising a colored core and a coating adapted to allow light to pass through and a matrix based on metalloid or metal oxide, said matrix being adapted to allow light to pass through.

Provided are construction material granules. In one embodiment, the granules include a core enclosed by a layer comprising a conductive material and a layer comprising a dielectric material. Also provided are related methods of constructing such materials.

Provided are construction material granules. In one embodiment, the granules include a core enclosed by a layer comprising a conductive material and a layer comprising a dielectric material. Also provided are related methods of constructing such materials.

Nanoplatelet forms of metal hydroxide and metal oxide are provided, as well as methods for preparing same. The nanoplatelets are suitable for use as fire retardants and as agents for chemical or biological decontamination.

Disclosed is a composition having a substrate comprising metal oxide particles. The substrate has a coating thereon that includes an organic dispersant present in a amount that renders the substrate self-dispersible. Also disclosed is a composition, such as a cosmetic composition, that includes that self-dispersible coated substrate, and a process that includes coating a particulate metal oxide with an organic dispersant to render the metal oxide self dispersible.

The present invention relates to a process for preparing chromium(III) oxide by reaction of alkali metal chromate with gaseous ammonia, subsequent hydrolysis, isolation of the hydrolysis product and calcination.

The present invention relates to ester-coated core particles, thermoplastic polymer composition comprising a thermo-plastic polymer and such coated particles, a method for producing ester coated particles and the use of compositions of the invention as fillers or pigments with improved dispersion properties and pourability.

A solid composite material (16) combining: an inorganic pigment (10) in the form of discrete particles each comprising a colored core and a coating adapted to allow light to pass through; and a matrix (12) based on metalloid or metal oxide, said matrix being adapted to allow light to pass through.

Process for preparing chromium(III) oxide, which comprises the steps: a) reaction of sodium monochromate with gaseous ammonia, in particular at a temperature of from 200 to 800 C., b) hydrolysis of the reaction product obtained in step a) with the pH of the water for the hydrolysis being reduced before the hydrolysis or that of the alkaline mother liquor being reduced during or after the hydrolysis, to a value of from 4 to 11, preferably from 5 to 10, by means of an acid, c) isolation of the hydrolysis product which has precipitated in step b), preferably at a pH of from 4 to 11, in particular from 5 to 10, and optionally washing and optionally drying and d) calcination of the hydrolysis product obtained in step c) at a temperature of from 700 to 1400 C., in particular from 800 to 1300 C.