This invention has an object to provide a means for providing a calcium phosphate sintered body particle group that does not cause a phenomenon of bubble generation in any use mode thereof, and further has a smaller particle diameter. There is provided a ceramic particle group containing spherical ceramic particles, which is characterized in that the ceramic particle has a particle diameter within a range of 10 nm to 700 nm, and is a calcium phosphate sintered body particle, and further the ceramic particle group contains no calcium carbonate.

An abrasive particle having a body and a coating overlying the body, the coating including an amorphous material and at least one filler contained within the amorphous material. The abrasive particle may be included in a fixed abrasive article.

Passivated silicon-carbon composite materials and related processes are disclosed that overcome the challenges for providing amorphous nano-sized silicon entrained within porous carbon. Compared to other, inferior materials and processes described in the prior art, the materials and processes disclosed herein find superior utility in various applications, including energy storage devices such as lithium ion batteries.

A decorated particle comprises a single inorganic particle core having an uneven outer surface with a plurality of crevices and an average particle diameter of 20 to 150 microns. A binder retaining decorating particles is disposed on at least a portion of the outer surface of the inorganic particle core and fills the crevices. The decorating particles have an average particle diameter of 0.05 to 10 microns. A method of making decorated particles is also disclosed.

The present invention discloses a crystalline aluminum phosphite, a preparation method thereof and an application thereof as or for the preparation of a flame retardant or a flame retardant synergist. The preparation method has the following processes: 1, reacting aluminum hydrogen phosphite with an aluminum-containing compound in water at 80-110° C. to obtain a precipitate in the presence of no strong acid or a small amount of strong acid; 2, washing and filtering the precipitate; 3, drying the precipitate at 100-130° C.; 4, continuously heating the dried solid step by step at a low speed, where the material temperature is increased to not exceeding 350° C. from room temperature at about 5-10 h, with a temperature rise rate not exceeding 5° C./min. Compared with amorphous aluminum hydrogen phosphite, the crystalline aluminum phosphite has a higher thermal decomposition temperature, lower water absorption and weaker acidity, and can be synergistic with diethyl aluminum hypophosphite to achieve better flame retardant property and thus, is used for a halogen-free flame retardant component of high polymer materials.

The disclosure relates to a method for producing a solid-state lithium ion conductor material in which the use of water and/or steam is a medium when the obtained intermediate product is cooled or quenched and, if needed, comminution of the intermediate product and/or carrying out of a cooling process with the production of a powder in one comminution step or in a plurality of comminution steps leads or lead to especially advantageous production products. The subject of the disclosure is also the solid-state lithium ion conductor material that has an ion conductivity of at least 10.sup.−5 S/cm at room temperature as well as a water content of <1.0 wt %. The disclosure further relates to the use of the solid-state lithium ion conductor material in the form of a powder in batteries or rechargeable batteries, preferably lithium batteries or rechargeable lithium batteries, in particular, separators, cathodes, anodes, or solid-state electrolytes.

A method of recovering desalinated activated alumina (AA) beads from a composition including salt laden (high salt absorbed) activated alumna (AA) beads and free anions and free cations, comprising the step of electrodialysis of the composition to reduce salt content of the activated alumina (AA) beads to produce a stream comprising the desalinated activated alumina (AA) beads.

An amorphous silica powder that is suitable for obtaining a solid sealant that exhibits superior fluidity and filling properties, and a resin composition obtained by using the amorphous silica powder as a filler. An amorphous silica powder is prepared so as to have a modal diameter within the range of 1 to 10 μm in the particle diameter frequency distribution and have a frequency of particles having particle diameters of 0.50 to 1.83 μm of less than 3.0% in the particle diameter frequency distribution.

A device for treating roof runoff has a first tube adapted to be axially aligned with, and in fluid communication with, an outlet of a downpipe. The first tube contains a crushed calcium carbonate media. The device has a second tube in fluid communication with the first tube. The first tube and second tube are arranged such that when a flow of roof runoff from the downpipe is at or below a predetermined flow rate, the flow of roof runoff is directed into the first tube to be treated by the crushed calcium carbonate media contained therein, and when the flow of roof runoff is above the predetermined flow rate, excess flow is diverted into the second tube.

Metal oxide gel particles, may be prepared with a desired particle size, by preparing a low-temperature aqueous metal nitrate solution containing hexamethylene tetramine as a feed solution; and causing the feed solution to flow through a first tube and exit the first tube as a first stream at a first flow rate, so as to contact a high-temperature nonaqueous drive fluid. The drive fluid flows through a second tube at a second flow rate. Shear between the first stream and the drive fluid breaks the first stream into particles of the metal nitrate solution, and decomposition of hexamethylene tetramine converts metal nitrate solution particles into metal oxide gel particles. A metal oxide gel particle size is measured optically, using a sensor device directed at a flow of metal oxide gel particles within the stream of drive fluid. The sensor device measures transmission of light absorbed by either the metal oxide gel particles or the drive fluid, so that transmission of light through the drive fluid changes for a period of time as a metal oxide gel particle passes the optical sensor. If a measured particle size is not about equal to a desired particle size, the particle size may be corrected by adjusting a ratio of the first flow rate to a total flow rate, where the total flow rate is the sum of the first and second flow rates.