The present disclosure provides a system and method for granulating and molding silicon liquid. The system includes a silicon liquid transferring device, wherein cooling system and a lifting system matching with the cooling system are provided below the silicon liquid transferring device. The silicon liquid transferring device transfers smelted silicon liquid to a position above the cooling system, uniformly pours the silicon liquid into the cooling system according a set flow to enable the silicon liquid to be solidified into silicon pellets, and then the molded silicon pellets are extracted by the lifting system, solving the problem in the prior art of irregular molding and inconsistent size of silicon blocks caused by pouring. A container bottom and a diversion pipe are set to be of detachable structures, and can be quickly disassembled and assembled as vulnerable parts without affecting the production.

The present invention relates to extended release microparticles comprising a drug, and a preparation method therefor, and when the extended release microparticles comprising a drug are administered in order to replace conventional drugs that should be administered daily or monthly, the drug administration effect can be continuously maintained for one week to three months. In addition, the drug administration effect is maintained for a long time and, simultaneously, microparticles are prepared so as to have the average diameter of a fixed micro-size, and thus an effective drug concentration can be constantly maintained by controlling the release of the drug from the microparticles, and a foreign body sensation and pain can be reduced during drug administration since microparticles having a uniform size are included during application as an injectable drug.

A method for producing an electrically-conductive pellet includes reducing a size of a first material. The method also includes wetting the first material to produce a first slurry. The method also includes introducing the first slurry into a fluidizer to produce a first pellet. The method also includes reducing a size of a second material. The second material is an electrically-conductive material. The method also includes wetting the second material to produce a second slurry. The method also includes applying the second slurry to the first pellet.

A method for producing an electrically-conductive pellet includes reducing a size of a first material. The method also includes wetting the first material to produce a first slurry. The method also includes introducing the first slurry into a fluidizer to produce a first pellet. The method also includes reducing a size of a second material. The second material is an electrically-conductive material. The method also includes wetting the second material to produce a second slurry. The method also includes applying the second slurry to the first pellet.

Nano- to microscale liquid coacervate particles are provided. The liquid coacervate particles are produced by a process including stimulating a population of liquid droplets containing one or a mixture of components to induce a phase separation point of a first component, and maintaining stimulation at the phase separation point to form a coacervate domain of the first component within each of the droplets to form the liquid coacervate particles. The self-assembled nano, meso, micro and macro liquid coacervate particles and related coated substrates can have utility in drug delivery, bioanalytical systems, controlled cell culture, tissue engineering, biomanufacturing and drug discovery.

Nano- to microscale liquid coacervate particles are provided. The liquid coacervate particles are produced by a process including stimulating a population of liquid droplets containing one or a mixture of components to induce a phase separation point of a first component, and maintaining stimulation at the phase separation point to form a coacervate domain of the first component within each of the droplets to form the liquid coacervate particles. The self-assembled nano, meso, micro and macro liquid coacervate particles and related coated substrates can have utility in drug delivery, bioanalytical systems, controlled cell culture, tissue engineering, biomanufacturing and drug discovery.

Provided is a wet atomizer for processing all-solid-state battery raw materials while ensuring sealing property, operability after completion of processing, and maintenance property. The wet atomizer includes a liquid supply pump for supplying the all-solid-state battery raw materials, a pressure intensifier for pressurizing the all-solid-state battery raw materials supplied from the liquid supply pump, a high-pressure filter for filtering the all-solid-state battery raw materials pressurized by the pressure intensifier, a chamber for injecting the all-solid-state battery raw materials filtered by the high-pressure filter, a sealing member for sealing the space for processing the all-solid-state battery raw materials, and an inert gas supply unit for supplying an inert gas to the sealing member.

Provided is a wet atomizer for processing all-solid-state battery raw materials while ensuring sealing property, operability after completion of processing, and maintenance property. The wet atomizer includes a liquid supply pump for supplying the all-solid-state battery raw materials, a pressure intensifier for pressurizing the all-solid-state battery raw materials supplied from the liquid supply pump, a high-pressure filter for filtering the all-solid-state battery raw materials pressurized by the pressure intensifier, a chamber for injecting the all-solid-state battery raw materials filtered by the high-pressure filter, a sealing member for sealing the space for processing the all-solid-state battery raw materials, and an inert gas supply unit for supplying an inert gas to the sealing member.

Methods of high throughput hydrocolloid bead production and related apparatuses are described herein. In the disclosed methods, drops of a hydrocolloid gel suspension are dropped into a reactant bath. The drops of hydrocolloid gel are exposed to the reactant bath for a predetermined period of time, during which the drops form firm or semi-firm beads. The beads are then removed from the reactant bath. The resulting hydrocolloid beads are advantageously resistant to syneresis and can provide high nutritional and water content.

Methods of high throughput hydrocolloid bead production and related apparatuses are described herein. In the disclosed methods, drops of a hydrocolloid gel suspension are dropped into a reactant bath. The drops of hydrocolloid gel are exposed to the reactant bath for a predetermined period of time, during which the drops form firm or semi-firm beads. The beads are then removed from the reactant bath. The resulting hydrocolloid beads are advantageously resistant to syneresis and can provide high nutritional and water content.