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356 results about "Reaction site" patented technology

An injection site reaction is inflammation in or damage to the tissue surrounding where a drug was injected. There are two types of injection site reactions: a local allergic reaction called a flare reaction, and a more severe reaction characterized by damage to the tissue due to extravasation.

Fluorocarbon emulsion stabilizing surfactants

Surfactants (e.g., fluorosurfactants) for stabilizing aqueous or hydrocarbon droplets in a fluorophilic continuous phase are presented. In some embodiments, fluorosurfactants include a fluorophilic tail soluble in a fluorophilic (e.g., fluorocarbon) continuous phase, and a headgroup soluble in either an aqueous phase or a lipophilic (e.g., hydrocarbon) phase. The combination of a fluorophilic tail and a headgroup may be chosen so as to create a surfactant with a suitable geometry for forming stabilized reverse emulsion droplets having a disperse aqueous or lipophilic phase in a continuous, fluorophilic phase. In some embodiments, the headgroup is preferably non-ionic and can prevent or limit the adsorption of molecules at the interface between the surfactant and the discontinuous phase. This configuration can allow the droplet to serve, for example, as a reaction site for certain chemical and / or biological reactions. In another embodiment, aqueous droplets are stabilized in a fluorocarbon phase at least in part by the electrostatic attraction of two oppositely charged or polar components, one of which is at least partially soluble in the dispersed phase, the other at least partially soluble in the continuous phase. One component may provide collodial stability of the emulsion, and the other may prevent the adsorption of biomolecules at the interface between a component and the discontinous phase. Advantageously, surfactants and surfactant combinations of the invention may provide sufficient stabilization against coalescence of droplets, without interfering with processes that can be carried out inside the droplets.
Owner:BIO RAD LAB INC +2

Method of manufacturing thermoplastic resin, crosslinked resin, and crosslinked resin composite material

The invention relates to a process for the production of post-crosslinkable thermoplastic resins by bulk-polymerizing a polymerizable composition (A) comprising (I) a monomer fluid containing a cyclic olefin (α) having two or more metathetical ring-opening reaction sites in the molecule in an amount 10 wt % or above based on the total amount of the monomers or a monomer fluid containing a norbornene monomer and a crosslinking agent, (II) a metathetical polymerization catalyst, and (III) a chain transfer agent; thermoplastic resins obtained by this process; and a process for producing crosslinked resins or crosslinked resin composite materials which comprises laminating such a thermoplastic resin with a substrate at need and then crosslinking the thermoplastic resin. According to the invention, thermoplastic resins which are free from odor due to residual monomers and excellent in storage stability can be efficiently obtained by a simple process of bulk-polymerizing the composition (A). The process is not only easy and simple but also applicable to continuous production, thus being industrially advantageous. The crosslinked resins and crosslinked resin composite materials obtained according to the invention are excellent in electrical insulation properties, mechanical strengths, heat resistance, dielectric characteristics and so on, thus being useful as electrical materials or the like.
Owner:ZEON CORP

Nitrogen-defect graphite-phase carbon nitride nanosheet photocatalyst, method for preparing same and application

The invention discloses a nitrogen-defect graphite-phase carbon nitride nanosheet photocatalyst, a method for preparing the same and application. The method includes 1), placing nitrogen-rich organicmatters such as melamine, dicyandiamide and thiourea urea into crucibles, keeping carrying out high-temperature calcination treatment on the nitrogen-rich organic matters at the temperatures ranging from 220-420 DEG C for 0.5-10 h, and carrying out cooling to obtain precursors; 2), grinding the precursors, and calcining the precursors in inert gas environments to obtain a product which is the nitrogen-defect graphite-phase carbon nitride nanosheet photocatalyst. The nitrogen-defect graphite-phase carbon nitride nanosheet photocatalyst, the method and the application have the advantages that large quantities of catalytic reaction sites can be provided by nitrogen-defect graphite-phase carbon nitride nanometer materials prepared by the aid of the method, photo-induced electrons can be trapped by nitrogen defects, photo-induced electron-hole separation can be effectively carried out, the composition rate can be reduced, and the photocatalytic activity can be improved; organic pollutants can be effectively degraded by the nitrogen-defect graphite-phase carbon nitride nanosheet photocatalyst in visible light irradiation.
Owner:LIAONING UNIVERSITY
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