36 results about "Nanoparticle Production" patented technology

Methods are described that have the capability of producing submicron/nanoscale particles, in some embodiments dispersible, at high production rates. In some embodiments, the methods result in the production of particles with an average diameter less than about 75 nanometers that are produced at a rate of at least about 35 grams per hour. In other embodiments, the particles are highly uniform. These methods can be used to form particle collections and/or powder coatings. Powder coatings and corresponding methods are described based on the deposition of highly uniform submicron/nanoscale particles.

The present disclosure relates to a nanoparticle production system and methods of using the system. The nanoparticle production system includes a plasma gun including a male electrode, a female electrodes and a working gas supply configured to deliver a working gas in a vortexing helical flow direction across a plasma generation region. The system also includes a continuous feed systems, a quench chamber, a cooling conduit that includes a laminar flow disruptor, a system overpressure module, and a conditioning fluid purification and recirculation system.

A method for generating nanoparticles in a liquid comprises generating groups of ultrafast laser pulses, each pulse in a group having a pulse duration of from 10 femtoseconds to 200 picoseconds, and each group containing a plurality of pulses with a pulse separation of 1 to 100 nanoseconds and directing the groups of pulses at a target material in a liquid to ablate it. The multiple pulse group ablation produces nanoparticles with a reduced average size, a narrow size distribution, and improved production efficiency compared to prior pulsed ablation systems.

Antitumor formulation based on nanoparticles of paclitaxel and human serum albumin as obtained by the addition of a biocompatible acid to an aqueous albumin solution before this is mixed with paclitaxel during the nanoparticle production process, the injectable solutions of this formulation having a pH between 5.4 and 5.8 and having stability and inalterability with time.

There is provided a method for the enhanced production of fullerenes, nanotubes and nanoparticles. The method relies upon the provision of a hydrocarbon liquid which is converted by a suitable energy source to a synthesis gas such as acetone, ethylene, methane or carbon monoxide, the synthesis gas(es) forming the precursors need for fullerene, nanotube or nanoparticle production. The nanotubes formed by the method described are in general terms shorter and wider than conventionally produced nanotubes. An improved apparatus for production of the fullerenes and nanocarbons is also disclosed wherein a moveable contactor is attached to a first electrode with a sealable chamber, and is spaced from the second electrode such that an electric arc can pass between them.

The present disclosure relates to a nanoparticle production system and methods of using the system. The nanoparticle production system includes a plasma gun including a male electrode, a female electrodes and a working gas supply configured to deliver a working gas in a vortexing helical flow direction across a plasma generation region. The system also includes a continuous feed system, a quench chamber, a cooling conduit that includes a laminar flow disruptor, a system overpressure module, and a conditioning fluid purification and recirculation system.

With this invention, in a nanoparticle production method, wherein nanoparticles are produced by irradiating a laser light irradiation portion 2a of a to-be-treated liquid 8 with a laser light, in which suspended particles are suspended, to pulverize the suspended particles in laser light irradiation portion 2a, laser light irradiation portion 2a of to-be-treated liquid 8 is cooled. In this case, by the cooling of to-be-treated liquid 8, the respective suspended particles are cooled in their entireties. When the portion 2a of this to-be-treated liquid 8 is irradiated with the laser light, the laser light is absorbed at the surfaces of the suspended particles at portion 2a. Since to-be-treated liquid 8 is cooled during this process, significant temperature differences arise between the interiors and surfaces of the suspended particles and between the surfaces of the suspended particles and the to-be-treated liquid at laser light irradiation portion 2a, and highly efficient nanoparticulation is realized.

The present disclosure is directed towards improved systems and methods for large-scale production of nanoparticles used for delivery of therapeutic material. The apparatus can be used to manufacturea wide array of nanoparticles containing therapeutic material including, but not limited to, lipid nanoparticles and polymer nanoparticles. In certain embodiments, continuous flow operation and parallelization of microfluidic mixers contribute to increased nanoparticle production volume.

The various embodiments herein provide a system and method for enhancing polymerization and nanoparticles production using a disc reactor. The system comprises of a rotating disc comprising a first surface and a second surface arranged longitudinally along a single axis of rotation, a shaft attached to the rotating disc, a ring provided across the first surface and the second surface of the rotating disc, at least one feed inlet for providing a feed solution, a fluid inlet for providing a heat transfer fluid, a fluid outlet for exiting the heat transfer fluid, a product collector for collecting the produced nanoparticles and a product outlet for exiting the produced nanoparticles. The feed solution flows from the first surface to the second surface of the rotating disc due to centrifugal forces and gets accumulated on the product collector and exits from the disc reactor through the product outlet.

The invention discloses a method for producing antibacterial silk through adding nanoparticles. The method comprises the following steps of evenly spraying a dispersion liquid of amino acid surface-modified nanoparticles on silkworm food, or directly mixing the amino acid surface-modified nanoparticles with the silkworm food evenly to obtain the silkworm food containing nanoparticles; feeding silkworms with the silkworm food containing the nanoparticles from the fifth instar of the silkworms until the silkworms stop eating; and spinning silk and cocooning by the silkworms and obtaining an antibacterial silk fiber containing the amino acid surface-modified nanoparticles. By adopting the method disclosed by the invention, the silk fiber and related products with excellent antibacterial property can be obtained.

Provided is an organic nanoparticle production method comprising a step in which a mixture of beads having an average particle size at least 0.15 mm and no more than a value (mm) calculated by the formula 1.07−0.11×[outer peripheral speed of the stirring rotor (m/sec)] and a slurry containing organic particles is stirred by a stirring rotor rotating at an outer peripheral speed of 7 m/sec or less in a vessel of a wet bead mill.

The present invention provides a process for producing nanoparticles, comprising: providing a first liquid comprising a metal salt and at least one species of ligand having a functional group capable of binding to a metal surface, providing a second liquid comprising a reducing agent; providing at least one liquid droplet generator operable to generate liquid droplets, causing the at least one liquid droplet generator to form liquid droplets of the first liquid, passing the liquid droplets through a gas to contact the second liquid so as to cause the metal salt and the at least one species of ligand to come into contact with the reducing agent, thereby causing self-assembly of nanoparticles, said nanoparticles having a core of said metal and a corona comprising a plurality of said ligands covalently bound to the core. Also provided are nanoparticles produced by the process of the invention and use of such nano particles in medicine.