A flame-retardant ultraviolet-resistant aramid fiber, the preparation method therefor comprising the following steps: adding nanoparticles into a hydrogen peroxide solution, performing magnetic stirring for 0.5-1 h, adding a sulfuric acid solution, and further performing magnetic stirring for 0.5 h; performing filtering to obtain a filter cake, and washing the filter cake with water and drying same to obtain modified particles; modifying the modified particles with curcumin and dopamine to obtain organic substance-modified particles; and finally subjecting the organic substance-modified particles to a reaction with a silicon methoxylated aramid fiber, so as to obtain a surface-modified aramid fiber. The present invention has high ultraviolet absorption and extremely low catalytic activity, avoiding damage to a fiber structure by photocatalysis in a radiation process, and in particular improving flame retardancy of the aramid fiber.

A flame-retardant ultraviolet-resistant aramid fiber, the preparation method therefor comprising the following steps: adding nanoparticles into a hydrogen peroxide solution, performing magnetic stirring for 0.5-1 h, adding a sulfuric acid solution, and further performing magnetic stirring for 0.5 h; performing filtering to obtain a filter cake, and washing the filter cake with water and drying same to obtain modified particles; modifying the modified particles with curcumin and dopamine to obtain organic substance-modified particles; and finally subjecting the organic substance-modified particles to a reaction with a silicon methoxylated aramid fiber, so as to obtain a surface-modified aramid fiber. The present invention has high ultraviolet absorption and extremely low catalytic activity, avoiding damage to a fiber structure by photocatalysis in a radiation process, and in particular improving flame retardancy of the aramid fiber.

Sizing agent coated carbon fibers obtained by coating carbon fibers with a sizing agent comprising at least one of (A) to (C) in a total amount of 80 mass % or more with respect to the whole sizing agent, the carbon fibers each having a surface layer which has a thickness of 10 nm or larger and has an oxygen content of 4% or higher with respect to all the elements, wherein when the sizing agent coated carbon fibers are subjected three times to a 10-minute ultrasonic treatment in an acetone solvent, then the amount of the remaining sizing agent is 0.1-0.25 parts by mass per 100 parts by mass of the sizing agent coated carbon fibers. (A) At least one polymer selected from the group consisting of polyimides, polyetherimides, and polysulfones (B) A compound having a terminal unsaturated group and a polar group in the molecule (C) A polyether-type aliphatic epoxy compound and/or a polyol-type aliphatic epoxy compound which each have an epoxy equivalent of 250 g/eq or less and have two or more epoxy groups in the molecule

Sizing agent coated carbon fibers obtained by coating carbon fibers with a sizing agent comprising at least one of (A) to (C) in a total amount of 80 mass % or more with respect to the whole sizing agent, the carbon fibers each having a surface layer which has a thickness of 10 nm or larger and has an oxygen content of 4% or higher with respect to all the elements, wherein when the sizing agent coated carbon fibers are subjected three times to a 10-minute ultrasonic treatment in an acetone solvent, then the amount of the remaining sizing agent is 0.1-0.25 parts by mass per 100 parts by mass of the sizing agent coated carbon fibers. (A) At least one polymer selected from the group consisting of polyimides, polyetherimides, and polysulfones (B) A compound having a terminal unsaturated group and a polar group in the molecule (C) A polyether-type aliphatic epoxy compound and/or a polyol-type aliphatic epoxy compound which each have an epoxy equivalent of 250 g/eq or less and have two or more epoxy groups in the molecule

The present invention relates to surface-modified polyolefin fibers, the use of these fibers in hydraulic binder compositions, hydraulic binder compositions containing these fibers and a method for reinforcing hydraulic binder compositions.

The present invention relates to surface-modified polyolefin fibers, the use of these fibers in hydraulic binder compositions, hydraulic binder compositions containing these fibers and a method for reinforcing hydraulic binder compositions.

Methods for treating a garment include: prewashing the garment; drying the garment in a first drying process; spraying a functional chemical onto the dried garment; and applying a curing treatment to the garment to cure the functional chemical. The method may further include drying the garment in a second drying process after spraying the functional chemical onto the garment.

Methods for treating a garment include: prewashing the garment; drying the garment in a first drying process; spraying a functional chemical onto the dried garment; and applying a curing treatment to the garment to cure the functional chemical. The method may further include drying the garment in a second drying process after spraying the functional chemical onto the garment.

A welding process may be configured to convert a substrate into a welded substrate by applying a process solvent to the substrate, wherein the process solvent interrupts one or more intermolecular force between one or more component in the substrate. The substrate may be configured as a natural fiber, such as cellulose, hemicelluloses, and silk. The process solvent may be configured as an ionic-liquid based solvent and the welded substrate may be a congealed network after the process solvent has been adequately swollen and/or mobilized the substrate. A welding process may be configured such that individual fibers of a substrate are not fully dissolved such that material in the fiber core may be left in the native state by controlling process variables. The welding process fibers may have a tenacity 10% or 20% greater or a diameter 25% less than that of a cellulosic-based yarn substrate.

A welding process may be configured to convert a substrate into a welded substrate by applying a process solvent to the substrate, wherein the process solvent interrupts one or more intermolecular force between one or more component in the substrate. The substrate may be configured as a natural fiber, such as cellulose, hemicelluloses, and silk. The process solvent may be configured as an ionic-liquid based solvent and the welded substrate may be a congealed network after the process solvent has been adequately swollen and/or mobilized the substrate. A welding process may be configured such that individual fibers of a substrate are not fully dissolved such that material in the fiber core may be left in the native state by controlling process variables. The welding process fibers may have a tenacity 10% or 20% greater or a diameter 25% less than that of a cellulosic-based yarn substrate.