Abstract:
Provided are a thermoplastic elastomer composition containing 100 parts by mass of (a) a specified hydrogenated block copolymer and 0.01 to 5 parts by mass of (b) at least one additive selected from an antioxidant and a light stabilizer, wherein the additive (b) is soluble in toluene at room temperature, and the additive (b) exists in the inside and on the surface of the pellet; and a molded article formed from the pellet.
Abstract:
Various embodiments disclosed relate to melt-stabilized ultra high molecular weight antioxidant, methods of making the same, and medical implants made from the same. In various embodiments, the present invention provides a method of melt-stabilizing ultra high molecular weight polyethylene (UHMWPE). The method can include coating a solid material including LIMA/PE with an antioxidant, to provide an antioxidant-coated solid material. The method can include pre-irradiatively heating the antioxidant-coated solid material to diffuse the antioxidant therein, to provide an antioxidant-diffused solid material. The method can include irradiating the antioxidant-diffused solid material, to provide an irradiated solid material. The method can include post-irradiatively heating the irradiated solid material, the heating sufficient to melt at least part of the UHMWPE, to provide a heated material. The method can also include solidifying the heated material, to provide a melt-stabilized material.
Abstract:
Methods for the preparation of polymer-templated core-shell nanoparticles include the steps of (a) preparing a cationic polymeric core material comprising polymeric micelles, and (b) coating the core material with a silica-comprising shell by depositing the shell onto the polymeric micelles from at least one silica precursor to form the core-shell nanoparticles. Compositions which include the core-shell nanoparticles are adapted to facilitate controlled delivery of at least one active agent into a system in response to controlled changes in the pH of the system.
Abstract:
High-melting antimicrobial polymer fibers and antimicrobial fabrics comprising such fibers are prepared by preparing a masterbatch of polymer pellets (e.g., PET), silver and copper salts, and a compounding agent which provides free flowing polymer pellets which can be prepared in advance, with a long shelf life. Polymer masterbatches prepared by the methods of the invention can produce limited color or off-white antimicrobial fibers and fabrics using conventional melt spinning manufacturing methods. Fabrics incorporating fibers of the present invention are potent inhibitors of Athlete's foot fungi, gram negative and gram positive bacteria, and drug resistant pathogens.
Abstract:
Disclosed are the nanoparticle and the method for the same, and the preparing method includes steps of mixing polyethylenimine (PEI) with the poly(acrylic acid)-bound iron oxide (PAAIO) to form a PEI-PAAIO polyelectrolyte complex (PEC) and mixing the PEI-PAAIO PEC with genetic material such as plasmid DNA to form the PEI-PAAIO/pDNA magnetic nanoparticle. The PEI-PAAIO/pDNA magnetoplex is highly water dispersible and suitable for long term storage, shows superparamagnetism, low cytotoxicity, high stability and nice transfection efficiency, and thus the PEI-PAAIO PEC can replace PEI as a non-viral gene vector.
Abstract:
The invention includes a system for solidification of liquid medical waste for use in connection with a vessel configured to receive an aqueous liquid to be solidified. The system includes an absorbent composition including a plurality of surface cross-linked superabsorbent particles and a plurality of second particles. Additionally, a soluble packet may be included so that the absorbent composition is released upon dissolution of the packet. The invention also includes a liquid solidification system for reducing gel block and a method of solidifying liquid medical waste.
Abstract:
Disclosed are the nanoparticle and the method for the same, and the preparing method includes steps of mixing polyethylenimine (PEI) with the poly(acrylic acid)-bound iron oxide (PAAIO) to form a PEI-PAAIO polyelectrolyte complex (PEC) and mixing the PEI-PAAIO PEC with genetic material such as plasmid DNA to form the PEI-PAAIO/pDNA magnetic nanoparticle. The PEI-PAAIO/pDNA magnetoplex is highly water dispersible and suitable for long term storage, shows superparamagnetism, low cytotoxicity, high stability and nice transfection efficiency, and thus the PEI-PAAIO PEC can replace PEI as a non-viral gene vector.
Abstract:
Reinforced copolymers formed from a functionalized copolymer that undergoes a reactive extrusion process with an inorganic component to form the reinforced copolymer. The functionalized copolymer in the form of a block and/or graft copolymer includes hard segments and soft segments, where the soft segments are covalently bonded with a coupling agent either before or after copolymerization with the hard segments. The reinforced copolymer of the present disclosure can be suitable for use as a biomaterial and/or in medical devices.
Abstract:
Exemplary embodiments provide intermediate transfer members that can be used in electrostatographic devices and methods for using them in forming an image. The disclosed intermediate transfer members can include a plurality of nanotubes with high electrical conductivity, high thermal conductivity, and/or low humidity sensitivity. The hydrophobicity of the nanotubes can be controlled by covalently grafting hydrophobic components onto one or more nanotubes; surface treating one or more nanotubes; and encapsulating one or more nanotubes with hydrophobic components. In an exemplary embodiment, the nanotubes can be dispersed in polymer matrices and/or formed on the surface of polymer matrices of the intermediate transfer members. The intermediate transfer members can take various forms of belts, sheets, webs, films, rolls, tubes or any shape that can provide a smooth surface and rotatable function.
Abstract:
A nontoxic micro anti-bacterial film coated with silver nano-particles and a method of manufacturing the same are disclosed. The method of manufacturing a non-toxic micro anti-bacterial film coated with silver nano-particles including the steps of: producing mixed/combined powers as anti-bacterial powders, thermosensitive or photosensitive ink capsule powers, and fragrant capsule powders, and silver nano powder are combined with an additive; producing solid powders as 20-50 weight % of the mixed/combined powders, and 50-80 weight % of olefin, acrylic or urethane binder are mixed and then disperse; producing a paste type of print ink as 30 weight % of the solid powders and 70 weight % of solvent are mixed; and printing the print ink on a thin film made of olefin resin, acrylic resin, and urethane resin, using a silk screen printing method, printing a predetermined design thereon. The designs of the non-toxic micro anti-bacterial film can be pressed and transferred to the stationery products or the necessaries of life. Therefore, users can obtain joy and interest from the products as designs are changed according to temperature change. Also, the non-toxic micro anti-bacterial film exhales fragrance and has anti-bacterial operation.