Provided is a preparation method of a coating material. The method includes: using an aluminum salt and a silicon source as precursors; and performing hydrothermal crystallization and calcination treatments successively under an action of a template agent to obtain the coating material, wherein the template agent is used to cause the coating material to form a porous spherical structure. In the embodiments of the present disclosure, the preparation process of the coating material is simple and the cost is low, and the specific surface area of the prepared coating material is large.

A nucleating agent composition, a method of forming the nucleating agent and a device comprising the nucleating agent composition are provided. The nucleating agent comprises a nucleating agent comprises silver halide salt with an average particle size of at least 10 nanometer to no more than 100 microns in a polymeric matrix wherein the polymeric matrix has a viscosity of at least 500 cP to no more than 50,000 cP.

A nucleating agent composition, a method of forming the nucleating agent and a device comprising the nucleating agent composition are provided. The nucleating agent comprises a nucleating agent comprises silver halide salt with an average particle size of at least 10 nanometer to no more than 100 microns in a polymeric matrix wherein the polymeric matrix has a viscosity of at least 500 cP to no more than 50,000 cP.

A nucleating agent composition, a method of forming the nucleating agent and a device comprising the nucleating agent composition are provided. The nucleating agent comprises a nucleating agent comprises silver halide salt with an average particle size of at least 10 nanometer to no more than 100 microns in a polymeric matrix wherein the polymeric matrix has a viscosity of at least 500 cP to no more than 50,000 cP.

Porous and microporous parts prepared by additive manufacturing as disclosed herein are useful in medical and non-medical applications. The parts are prepared from a composition containing both a solvent soluble component and a solvent insoluble component. After a part is printed by an additive manufacturing process it is exposed to solvent to extract solvent soluble component away from the printed part, resulting in a part having surface cavities.

Porous and microporous parts prepared by additive manufacturing as disclosed herein are useful in medical and non-medical applications. The parts are prepared from a composition containing both a solvent soluble component and a solvent insoluble component. After a part is printed by an additive manufacturing process it is exposed to solvent to extract solvent soluble component away from the printed part, resulting in a part having surface cavities.

Provided are a polyamide resin having high crystallinity, a high glass transition temperature, and a low mass loss rate, and a polyamide resin composition and a molded article in which the polyamide resin is used. The polyamide resin includes a diamine-derived structural unit and a dicarboxylic acid-derived structural unit, in which 50 mol % or more of the diamine-derived structural units are structural unit derived from p-benzenediethanamine, and of the dicarboxylic acid-derived structural units, from not less than 20 mol % to less than 95 mol % are structural units derived from an aromatic dicarboxylic acid and from more than 5 mol % to not more than 80 mol % are structural units derived from an α,ω-linear aliphatic dicarboxylic acid having from 4 to 15 carbons.

Provided are a polyamide resin having high crystallinity, a high glass transition temperature, and a low mass loss rate, and a polyamide resin composition and a molded article in which the polyamide resin is used. The polyamide resin includes a diamine-derived structural unit and a dicarboxylic acid-derived structural unit, in which 50 mol % or more of the diamine-derived structural units are structural unit derived from p-benzenediethanamine, and of the dicarboxylic acid-derived structural units, from not less than 20 mol % to less than 95 mol % are structural units derived from an aromatic dicarboxylic acid and from more than 5 mol % to not more than 80 mol % are structural units derived from an α,ω-linear aliphatic dicarboxylic acid having from 4 to 15 carbons.

A solvent-free and ligand-free ball milling method for preparation of cesium lead tribromide (CsPbBr.sub.3) quantum dot is provided. First, mixing a Cs source, a Pb source, and a Br source as per a molar ratio of Cs source:Pb source:Br source is 1:1˜6:1˜9, and then adding polymethyl methacrylate (PMMA) to obtain a mixture. The mixture is milled for 1-2 hours at a rotation speed in a range of 360˜630 revolutions per minute (r/min) in a ball milling device, obtaining CsPbBr.sub.3 quantum dot. The method has advantages such as simple process, easy industrial production, no solvent, no organic ligand, low cost, and environmental protection. A quantum yield of product obtained by the method is up to 78%, and the product has a strong environmental stability. A preparation temperature of the product is low, and the reaction can be completed at a room temperature without a high temperature treatment.

A solvent-free and ligand-free ball milling method for preparation of cesium lead tribromide (CsPbBr.sub.3) quantum dot is provided. First, mixing a Cs source, a Pb source, and a Br source as per a molar ratio of Cs source:Pb source:Br source is 1:1˜6:1˜9, and then adding polymethyl methacrylate (PMMA) to obtain a mixture. The mixture is milled for 1-2 hours at a rotation speed in a range of 360˜630 revolutions per minute (r/min) in a ball milling device, obtaining CsPbBr.sub.3 quantum dot. The method has advantages such as simple process, easy industrial production, no solvent, no organic ligand, low cost, and environmental protection. A quantum yield of product obtained by the method is up to 78%, and the product has a strong environmental stability. A preparation temperature of the product is low, and the reaction can be completed at a room temperature without a high temperature treatment.