The present disclosure is drawn to a composite particulate build material, including 92 wt % to 99.5 wt % polymeric particles having an average size from 10 μm to 150 μm and an average aspect ratio of less than 2:1. The composite particulate build material further includes from 0.5 wt % to 8 wt % reinforcing particles having an average size of 0.1 μm to 20 μm and an average aspect ratio of 3:1 to 100:1 applied to a surface of the polymeric particles.

This disclosure provides a nano-graphitic sponge (NGS) and methods for preparing the nano-graphitic sponge. The disclosed nano-graphitic sponge possesses many excellent properties, including large surface areas and pore volumes, low-mass densities, good electrical conductivities and mechanical properties. These excellent properties make the nano-graphitic sponge an ideal material for many applications, such as electrodes for batteries and supercapacitors, fuel cells and solar cells, catalysts and catalyst supports, and sensors.

A prepreg which is suitable for producing a fiber-reinforced composite material in a short period of time without using an autoclave, can produce a fiber-reinforced composite material in which the occurrence of voids is suppressed and excellent impact resistance is achieved, and has excellent handling properties; and a fiber-reinforced composite material using the prepreg. This prepreg is a prepreg in which a reinforcing fiber [A] arranged in layers is partially impregnated with an epoxy resin composition containing an epoxy resin [B] and a curing agent [C], wherein the impregnation rate φ is 30-95%, and a thermoplastic resin [D] insoluble in the epoxy resin [B] is unevenly distributed on both surfaces of the prepreg. In addition, in the layers of the reinforcing fiber [A], epoxy resin composition-unimpregnated portions are localized on one surface of the prepreg, and the localization parameter a, which defines the degree of localization, is in the range of 0.10<σ<0.45.

The present invention relates to a composition for hydrogel formation, a hydrogel formed by photo-crosslinking same, and a method for preparing the hydrogel and, more specifically, to a composition which comprises a photo-initiator and a polyglutamic acid polymer having a photo-crosslinkable functional group introduced thereto and is capable of forming a hydrogel in real time through photo-crosslinking, to a hydrogel which is formed by photo-crosslinking the composition and can be utilized as a tissue adhesive, a surgical sealant, anti-adhesive agent, or the like due to excellent biocompatibility, superior adhesive strength in wet environments, flexibility, and ease of use, and to a method for preparing the hydrogel.

A process for the production of a masterbatch (M) which includes at least one lactam and at least one fiber material is provided herein. Also described herein is the masterbatch (M) and a polymerizable two-component system (pS), as well as a process for the production of a polyamide (P), the use of the masterbatch (M) for the production of the polyamide (P), and the polyamide (P). A molding made of the polyamide (P) is also described.

The use of a sealing layer of a composition including at least one polyamide for preparing a multicore structure intended for the transport, distribution or storage of hydrogen, in particular for the distribution or storage of hydrogen, especially for the storage of hydrogen, the sealing layer satisfying a test for contaminants present in the hydrogen and extracted from the sealing layer after contact of the hydrogen with same, the test been carried out as defined in the standard CSA/ANSI CHMC 2: 19, the total proportion of said contaminants extracted in the hydrogen being less than or equal to 3% by weight, in particular less than 2% by weight of the sum of the constituents of the composition.

The present disclosure is drawn to a composite particulate build material, including 92 wt % to 99.5 wt % polymeric particles having an average size from 10 μm to 150 μm and an average aspect ratio of less than 2:1. The composite particulate build material further includes from 0.5 wt % to 8 wt % reinforcing particles having an average size of 0.1 ρm to 20 μm and an average aspect ratio of 3:1 to 100:1 applied to surfaces of the polymeric particles, wherein the reinforcing particles include mica or glass.

The present invention relates to processes and systems for preparing nanoparticles, cellular or viral membranes and/or cellular or viral membrane coated nanoparticles using or comprising, inter alia, a multi-inlet vortexing reactor, tangential flow filtration (TFF) and/or a high shear fluid processor such as a microfluidizer (or a microfluidizer processor). The present invention also relates to the nanoparticles, cellular or viral membranes and/or cellular or viral membrane coated nanoparticles prepared by the present processes and systems, and the uses and/or applications of the nanoparticles, cellular or viral membranes and/or cellular or viral membrane coated nanoparticles.

A thermoplastic prepreg is disclosed having fully impregnated filaments. The prepreg is formed by having a plurality of continuous fibers that are substantially oriented in a longitudinal direction, the continuous fibers constituting from about 30 wt. % to about 40 wt. % of the prepreg, a first resinous matrix that contains a first set of one or more thermoplastic polymers and within which the continuous fibers are embedded, wherein the thermoplastic polymers constitute from about 30 wt. % to about 40 wt. % of the prepreg, and a second resinous matrix that contains a second set of one or more thermoplastic polymers, wherein the second set of thermoplastic polymers constitute from about 30 wt. % to about 40 wt. % of the prepreg.

Provided is a gas-barrier polyamide film that has excellent bending pinhole resistance and friction pinhole resistance at the same time, that has excellent gas barrier properties, and that is suitable for use for packaging materials. In addition, the environmental load is reduced by using a plant-derived resin as a raw material. A gas-harrier polyamide film comprising an inorganic thin film layer on at least one surface of a biaxially stretched polyamide film containing 99 to 70% by mass of a polyamide 6 resin and 1 to 30% by mass of a polyamide resin in which at least a part of raw material is derived from biomass.