Spherical crystalline silica particles having a higher productivity, lower production cost, higher coefficient of thermal expansion, higher heat transmission rate, higher fluidity, higher dispersability, higher fill factor, low abrasiveness, and higher purity compared with the past and able to be applied in the semiconductor field and a process of production of the same are provided. Spherical crystalline silica particles containing 400 to 5000 ppm of aluminum and containing 80% or more of crystal phases are provided.

Methods and apparatus are disclosed for producing seeds that are transformed into hollow spheres. A seed includes a core and a coating. Upon heating, the coating becomes viscous and expands responsive to an internal gas pressure created by the core. Example applications for the seeds and/or cores are disclosed, including bricks and other construction materials having the hollow spheres incorporated therein.

The present application provide a silicon-oxygen compound, a secondary battery using it, and related battery modules, battery packs, and devices. The silicon-oxygen compound provided by the present application has a formula of SiO.sub.x, in which x satisfies 0<x<2. The silicon-oxygen compound contains both sulfur and aluminum element, and the sulfur element is present in an amount of 20 ppm˜300 ppm. The mass ratio of sulfur element to aluminum element is from 1.5 to 13.0. A secondary battery uses the silicon-oxygen compound provided in the present application, so that the secondary battery can have both long-cycle performance and high initial coulombic efficiency.

The present invention relates to mesoporous silica embedded with alloy particles, and a preparation method thereof, and it is possible to prevent the release of metal particles to the outside because the inside of spherical mesoporous silica is embedded with metal nanoparticles, and as the aggregation of the metal is prevented, the stability is excellent and the production yield is high during the preparation process, so that mesoporous silica can be mass-produced, the efficacy of metal nanoparticles may be maintained by preventing the oxidation of metal nanoparticles, and mesoporous silica can be produced at low costs. Further, the inside of pores of mesoporous silica is embedded with metal nanoparticles, so that the discoloration and smell change phenomenon does not occur, and the far-infrared emission and deodorization effects are excellent.

A method for the preparation of an amorphous silica-alumina composition is provided that advantageously utilizes as a component oxidized disulfide oil, for example derived from a waste refinery stream of disulfide oil. The amorphous silica-alumina is formed from an aqueous mixture of an aluminum source, a silica source, oxidized disulfide oil, an alkali metal source and optionally a structure directing agent, which is heating under conditions and for a time effective to form the amorphous silica-alumina.

The present application provide a silicon-oxygen compound, a secondary battery using it, and related battery modules, battery packs, and devices. The silicon-oxygen compound provided by the present application has a formula of SiO.sub.x, in which x satisfies 0<x<2. The silicon-oxygen compound contains both sulfur and aluminum element, and the sulfur element is present in an amount of 20 ppm˜300 ppm. The mass ratio of sulfur element to aluminum element is from 1.5 to 13.0. A secondary battery uses the silicon-oxygen compound provided in the present application, so that the secondary battery can have both long-cycle performance and high initial coulombic efficiency.

A process for producing solar grade silicon from silica sand employs a plurality of plasma furnaces to perform a sequence of chemical reactions together with other process steps to produce solar grade silicon. The plasma furnace generates a stable dirty air, donutshaped plasma into which particulate matter can be introduced. The plasma in the first two stages is formed by gases from the chemical reactions and in the third from inert gasses. Cyclone separators are used to extract particulates from the plasma in an inert gas that prevents reverse reactions as the particular cools.

A terahertz material for emission reduction and fuel saving of gasoline vehicles and its preparation method and application, includes the following raw materials in parts by weight: 20˜35 SiO.sub.x, 3˜15 Al.sub.2O.sub.3, 25˜45 SiO.sub.2, 15˜25 Fe.sub.2O.sub.3, 20˜40 ochre, 0.5˜2 barium tungstate, 15˜25 CaCO.sub.3, wherein a preparation methodincludes: mixing the component raw materials according to the above ratio; after crushing, performing heating to 600˜1,200° C. in an oxygen-free environment, maintaining the temperature for 3˜8 hours, and then performing crushing for the second time; and performing enhancement processing with terahertz irradiation rays at 10 mW to 100 W for 5 seconds to 1 hour to obtain a terahertz material, wherein the terahertz material improves combustion efficiency by increasing the molecular activity of gasoline and air participating in combustion work and reducing molecular groups, and has the effects of emission reduction, energy saving and improving power.

The present invention relates to a method for synthesizing and collecting, in a single step, nanoparticles of different materials, and for producing coatings thereof on materials with simple or complex geometries, both in a controlled atmosphere and in ambient conditions, by means of the combined application of a laser beam and high-intensity electric fields.

Bisaminoalkoxysilanes of Formula I, and methods using same, are described herein:
R.sup.1Si(NR.sup.2R.sup.3)(NR.sup.4R.sup.5)OR.sup.6  I
where R.sup.1 is selected from hydrogen, a C.sub.1 to C.sub.10 linear alkyl group, a C.sub.3 to C.sub.10 branched alkyl group, a C.sub.3 to C.sub.10 cyclic alkyl group, a C.sub.3 to C.sub.10 alkenyl group, a C.sub.3 to C.sub.10 alkynyl group, a C.sub.4 to C.sub.10 aromatic hydrocarbon group; R.sup.2, R.sup.3, R.sup.4, and R.sup.5 are each independently selected from hydrogen, a C.sub.4 to C.sub.10 branched alkyl group, a C.sub.3 to C.sub.10 cyclic alkyl group, a C.sub.3 to C.sub.10 alkenyl group, a C.sub.3 to C.sub.10 alkynyl group, and a C.sub.4 to C.sub.10 aromatic hydrocarbon group; R.sup.6 is selected from a C.sub.1 to C.sub.10 linear alkyl group, a C.sub.3 to C.sub.10 branched alkyl group, a C.sub.3 to C.sub.10 cyclic alkyl group, a C.sub.3 to C.sub.10 alkenyl group, a C.sub.2 to C.sub.10 alkynyl group, and a C.sub.4 to C.sub.10 aromatic hydrocarbon group.