A molybdenum disulfide/graphene/carbon composite material having a hierarchical pore structure includes a composite nanofiber having a diameter of 60 to 500 nm. The composite nanofiber comprises, in mass percentage, 3% to 35% of molybdenum disulfide, 0.2% to 10% of graphene, and 60% to 95% of carbon. The composite nanofiber has a hierarchical pore structure distributed along the axial direction, and has a pore diameter continuously distributed between 0.1 nm and 5 μm and an average pore diameter between 1.5 nm and 25 nm. On the basis of the pore volume, in the hierarchical pore structure, a micropore structure accounts for 25% to 60%, and a mesoporous structure accounts for 40% to 75%. The microporous structure is distributed on the surface of the nanofiber and the pore wall of the mesoporous structure.

The resin composition for melt spinning of the present invention is a filament having a melt viscosity of 250 Pas or less at 200° C. and a shear rate of 0.1 s.sup.−1 and a tensile strength of 10 MPa or more. The filament can be produced by forming a molten liquid of a resin composition having a melt viscosity of 250 Pas or less at 200° C. and a shear rate of 0.1 s.sup.−1 into a filament shape to provide a formed material, and conveying and concurrently cooling the formed material. The present invention also provides a resin composition for melt spinning being a filament, and a method for producing fiber using a melt spinning apparatus.

Described herein are nanofibers and methods for making nanofibers that include any one or more of (a) a non-homogeneous charge density; (b) a plurality of regions of high charge density; and/or (c) charged nanoparticles or chargeable nanoparticles. In one aspect, the present invention fulfills a need for filtration media that are capable of both high performance (e.g., removal of particle sizes between 0.1 and 0.5 μm) with a low pressure drop, however the invention is not limited in this regard.

A method of producing a carbon fiber bundle is provided, involving performing a flame-proof treatment to a carbon-fiber-precursor acryl fiber bundle having a single-fiber fineness of 1.5 dtex or more and 5.0 dtex or less, and having a roundness of 0.7 or more and 0.9 or less in a cross-section shape perpendicular to a fiber axis of the single fiber to obtain a flame-proofed fiber bundle; and performing a carbonization treatment to the flame-proofed fiber bundle.

The present application provides low thickness synthetic elastomeric gloves, comprising (a) a thickness at the palm of less than 0.050 mm; (a) a modulus at 500% above 6.5 MPa; and/or (c) an elongation at break below 700%. Also provided is a method for the manufacture of such gloves involving dipping a glove-shaped former into an elastomeric film-forming composition; and curing the elastomeric film-forming composition on the former so as to produce the synthetic elastomeric glove. Corresponding low thickness finger cots are also described, as are formers suitable for the preparation of such gloves.

Methods of producing a nano-catalyst material including forming a plurality of nano-scale features on a surface of a substrate material. The nano-catalyst material may be used for forming anchored nanostructure materials by heating the nano-catalyst material under a protective atmosphere to a temperature ranging from about 450° C. to about 1500° C. and exposing the heated nano-catalyst to an organic vapor to affix a separate nanostructure to each of the plurality of nano-scale features. The nano-scale features may be formed on the surface of the substrate material by mechanical or thermal processes.

A modified kraft pulp fiber with unique properties is provided. The modified fiber can be a modified bleached kraft fiber that is almost indistinguishable from its conventional counterpart, except that it has a low degree of polymerization (DP). Methods for making the modified fiber and products made from it are also provided. The method can be a one step acidic, iron catalyzed peroxide treatment process that can be incorporated into a single stage of a multi-stage bleaching process. The products can be chemical cellulose feedstocks, microcrystalline cellulose feedstocks, fluff pulps and products made from them.

Polysaccharide filaments and fibrous structures containing such polysaccharide filaments and more particularly polysaccharide filaments that exhibit birefringence are provided.

Fibrous structures, for example sanitary tissue products, containing a plurality of filaments that employ one or more filament-forming materials, such as one or more hydroxyl polymers, and one or more hueing agents, present within the filaments such that the fibrous structures exhibit a Whiteness Index of greater than 72 as measured according to the Whiteness Index Test Method described herein.

Various embodiments of the present invention relate to surface enhanced pulp fibers, various products incorporating surface enhanced pulp fibers, and methods and systems for producing surface enhanced pulp fibers. Various embodiments of surface enhanced pulp fibers have significantly increased surface areas compared to conventional refined fibers while advantageously minimizing reductions in length following refinement. The surface enhanced pulp fibers can be incorporated into a number of products that might benefit from such properties including, for example, paper products, paperboard products, fiber cement boards, fiber reinforced plastics, fluff pulps, hydrogels, cellulose acetate products, and carboxymethyl cellulose products. In some embodiments, a plurality of surface enhanced pulp fibers have a length weighted average fiber length of at least about 0.3 millimeters and an average hydrodynamic specific surface area of at least about 10 square meters per gram, wherein the number of surface enhanced pulp fibers is at least 12,000 fibers/milligram on an oven-dry basis.