C01G9/02

METHOD FOR PREPARING A SELF-ASSEMBLED POROUS THREE-DIMENSIONAL ZINC OXIDE NANOPARTICLE STRUCTURE USING A MICROFLUIDIC DEVICE, ZINC OXIDE NANOPARTICLES, AN AGGREGATE OF ZINC OXIDE NANOPARTICLES, AND ZINC OXIDE NANOPARTICLE STRUCTURE PREPARED THEREFROM, AND A BIO-INK INCLUDING THE SAME
20220340441 · 2022-10-27 ·

The present application provides a method for preparing a zinc oxide nanoparticle structure synthesized using a microfluidic device and a self-assembled porous three-dimensional zinc oxide nanoparticle structure prepared therefrom. The self-assembled porous three-dimensional zinc oxide nanoparticle structure of the present application is a three-dimensional structure in which micropores, mesopores and macropores are created, and has excellent reactivity.

METHOD FOR PREPARING A SELF-ASSEMBLED POROUS THREE-DIMENSIONAL ZINC OXIDE NANOPARTICLE STRUCTURE USING A MICROFLUIDIC DEVICE, ZINC OXIDE NANOPARTICLES, AN AGGREGATE OF ZINC OXIDE NANOPARTICLES, AND ZINC OXIDE NANOPARTICLE STRUCTURE PREPARED THEREFROM, AND A BIO-INK INCLUDING THE SAME
20220340441 · 2022-10-27 ·

The present application provides a method for preparing a zinc oxide nanoparticle structure synthesized using a microfluidic device and a self-assembled porous three-dimensional zinc oxide nanoparticle structure prepared therefrom. The self-assembled porous three-dimensional zinc oxide nanoparticle structure of the present application is a three-dimensional structure in which micropores, mesopores and macropores are created, and has excellent reactivity.

Method for producing zinc oxide platelets with controlled size and morphology

A method for producing polygonic Zn oxide platelets having a median specific surface area of more than 25 square meters per gram, in controlled size and morphology, the method comprising: preparing a medium including Zn or its compounds at a concentration within the range between 1.55 and 7.75 moles of Zn/L, in a medium suitable to substitute Zn ions by releasing free protons thereby forming a complex structure including Zn; agitation of the medium in a vessel at a temperature within the range between 50 and 320° for a duration up to 10 hours to obtain a suspension; filtering the suspension to obtain a filtrate including solid particles; drying and then calcination of the dried filtrate; wherein the agitation is performed with one or more radial flow impellers so that the Reynolds' number in the vessel is higher than 2500 and lower than 10000.

Method for producing zinc oxide platelets with controlled size and morphology

A method for producing polygonic Zn oxide platelets having a median specific surface area of more than 25 square meters per gram, in controlled size and morphology, the method comprising: preparing a medium including Zn or its compounds at a concentration within the range between 1.55 and 7.75 moles of Zn/L, in a medium suitable to substitute Zn ions by releasing free protons thereby forming a complex structure including Zn; agitation of the medium in a vessel at a temperature within the range between 50 and 320° for a duration up to 10 hours to obtain a suspension; filtering the suspension to obtain a filtrate including solid particles; drying and then calcination of the dried filtrate; wherein the agitation is performed with one or more radial flow impellers so that the Reynolds' number in the vessel is higher than 2500 and lower than 10000.

Porous metal oxide microspheres with varying pore sizes

Porous metal oxide microspheres are prepared via a process comprising forming a liquid solution or dispersion of polydisperse polymer nanoparticles and a metal oxide; forming liquid droplets from the solution or dispersion; drying the liquid droplets to provide polymer template microspheres comprising polymer nanospheres and metal oxide; and removing the polymer nanospheres from the template microspheres to provide the porous metal oxide microspheres. The porous microspheres exhibit saturated colors and are suitable as colorants for a variety of end-uses.

Porous metal oxide microspheres with varying pore sizes

Porous metal oxide microspheres are prepared via a process comprising forming a liquid solution or dispersion of polydisperse polymer nanoparticles and a metal oxide; forming liquid droplets from the solution or dispersion; drying the liquid droplets to provide polymer template microspheres comprising polymer nanospheres and metal oxide; and removing the polymer nanospheres from the template microspheres to provide the porous metal oxide microspheres. The porous microspheres exhibit saturated colors and are suitable as colorants for a variety of end-uses.

COMPOSITE MATERIAL, QUANTUM DOT LIGHT-EMITTING DIODE AND PREPARATION METHOD THEREOF

A composite material, quantum dot light-emitting diode and preparation method thereof. The preparation method includes: providing ZnO nanoparticles and Au source, Au source is at least one of bulk Au or Au particles; mixing ZnO nanoparticles, Au source, S source with first organic solvent, performing hydrothermal reaction to prepare composite material. By performing hydrothermal reaction in organic solvent using ZnO nanoparticles, bulk Au and/or Au particles, and S source, S source can vulcanize surface of ZnO nanoparticles to form ZnS layer on surface of ZnO nanoparticles, Au source can be thermally dissolved and diffused into isolated distribution of atomic-level Au to realize loading on surface of ZnS layer, to obtain composite material with ZnO nanoparticles as core material, ZnS and Au as shell material. ZnS and Au in composite material can synergistically increase electron transmission efficiency of LED adopting same.

Method for obtaining encapsulated nanoparticles

A method for obtaining at least one particle, including: (a) preparing solution A including at least one precursor of at least one of Si, B, P, Ge, As, Al, Fe, Ti, Zr, Ni, Zn, Ca, Na, Ba, K, Mg, Pb, Ag, V, Te, Mn, Ir, Sc, Nb, Sn, Ce, Be, Ta, S, Se, N, F, and Cl; (b) preparing aqueous solution B; (c) forming droplets of solution A; (d) forming droplets of solution B; (e) mixing droplets; (f) dispersing mixed droplets in a gas flow; (g) heating dispersed droplets to obtain the at least one particle; (h) cooling the at least one particle; and (i) separating and collecting the at least one particle. The aqueous solution is acidic, neutral, or basic. In step (a) and/or step (b) at least one colloidal suspension of a plurality of nanoparticles is mixed with the solution. Also, a device for implementing the method.

Method for obtaining encapsulated nanoparticles

A method for obtaining at least one particle, including: (a) preparing solution A including at least one precursor of at least one of Si, B, P, Ge, As, Al, Fe, Ti, Zr, Ni, Zn, Ca, Na, Ba, K, Mg, Pb, Ag, V, Te, Mn, Ir, Sc, Nb, Sn, Ce, Be, Ta, S, Se, N, F, and Cl; (b) preparing aqueous solution B; (c) forming droplets of solution A; (d) forming droplets of solution B; (e) mixing droplets; (f) dispersing mixed droplets in a gas flow; (g) heating dispersed droplets to obtain the at least one particle; (h) cooling the at least one particle; and (i) separating and collecting the at least one particle. The aqueous solution is acidic, neutral, or basic. In step (a) and/or step (b) at least one colloidal suspension of a plurality of nanoparticles is mixed with the solution. Also, a device for implementing the method.

Solar light antibactertal agent

A composite nanomaterial of ZnO impregnated by, e.g., a green copper phthalocyanine compound (CuPc) can be an efficient solar light photocatalyst for water remediation. The composite may include hollow shell microspheres and hollow nanospheres of CuPc-ZnO. CuPc may function as a templating and/or structure modifying agent, e.g., for forming hollow microspheres and/or nanospheres of ZnO particles. The composite can photocatalyze the degradation of organic pollutants such as crystal violet (CV) and 2,4-dichlorophenoxyacetic acid as well as microbes in water under solar light irradiation. The ZnO—CuPc composite can be stable and recyclable under solar irradiation.