MXene fibers and a preparation method thereof are provided. The method for preparation of a MXene fiber comprises preparing a dope solution in which MXene sheets are dispersed in a polar solvent, extruding the dope solution into a coagulating solution to coagulate the extruded dope solution to change into a MXene gel fiber, and drying the MXene gel fiber and converting it into the MXene fiber.

Fabricating a multilayered polymer nanocomposite fiber includes injecting a first polymer solution and a second polymer solution to a head of spinneret to yield a two-layered fiber precursor in the spinneret, passing the two-layered fiber precursor through one or more multipliers in the spinneret to yield a multilayered fiber precursor having 2.sup.n+1 layers, passing the multilayered fiber precursor through a gap between an exit of the spinneret and into a coagulation bath, and coagulating the multilayered fiber precursor in the coagulation bath to yield a multilayered polymer nanocomposite fiber. The multilayered polymer nanocomposite fiber includes alternating layers of a first polymer formed from the first polymer solution and a second polymer formed from the second polymer solution. The second polymer solution includes carbon nanostructures.

An ultra-high molecular weight, ultra-fine particle size polyethylene has a viscosity average molecular weight (Mv) greater than 1×10.sup.6. The polyethylene is spherical or are sphere-like particles having a mean particle size of 10-100 μm, having a standard deviation of 2-15 μm and a bulk density of 0.1-0.3 g/mL. Using the polyethylene as a basic polyethylene, a grafted polyethylene can be obtained by means of a solid-phase grafting method; and a glass fiber-reinforced polyethylene composition comprising the polyethylene and glass fibers, and a sheet or pipe prepared therefrom; a solubilized ultra-high molecular weight, ultra-fine particle size polyethylene; and a fiber and a film prepared from the solubilized ultra-high molecular weight, ultra-fine particle size polyethylene may also be obtained. The method has simple steps, is easy to control, has a relatively low cost and a high repeatability, and can realize industrialisation.

An ultra-high molecular weight, ultra-fine particle size polyethylene has a viscosity average molecular weight (Mv) greater than 1×10.sup.6. The polyethylene is spherical or are sphere-like particles having a mean particle size of 10-100 μm, having a standard deviation of 2-15 μm and a bulk density of 0.1-0.3 g/mL. Using the polyethylene as a basic polyethylene, a grafted polyethylene can be obtained by means of a solid-phase grafting method; and a glass fiber-reinforced polyethylene composition comprising the polyethylene and glass fibers, and a sheet or pipe prepared therefrom; a solubilized ultra-high molecular weight, ultra-fine particle size polyethylene; and a fiber and a film prepared from the solubilized ultra-high molecular weight, ultra-fine particle size polyethylene may also be obtained. The method has simple steps, is easy to control, has a relatively low cost and a high repeatability, and can realize industrialisation.

Provided herein are high throughput continuous or semi-continuous reactors and processes for manufacturing expanded graphite materials. Such processes are suitable for manufacturing expanded graphite materials with little batch-to-batch variation.

Carbon fiber and method of forming the same are provided. The method modifies proportion of a finishing oil to control a relation between a surface tension and a particle size of the finishing oil, and thus penetration of the finishing oil into an interior of the carbon fiber is avoided. Therefore, the carbon fiber can have both low oil residues and a high strength.

Carbon fiber and method of forming the same are provided. The method modifies proportion of a finishing oil to control a relation between a surface tension and a particle size of the finishing oil, and thus penetration of the finishing oil into an interior of the carbon fiber is avoided. Therefore, the carbon fiber can have both low oil residues and a high strength.

Method of manufacturing a regenerated cellulosic molded body, wherein the method comprises supplying a starting material which comprises cellulose and at least one foreign matter, transferring at least a part of the starting material with at least a part of the at least one foreign matter into a spinning mass which additionally contains a solvent for solving at least a part of the cellulose of the starting material in the solvent, and extruding the spinning mass to the molded body, and subsequently precipitating in a spinning bath, wherein thereby the molded body is obtained, wherein the molded body comprises cellulose and at least a part of the at least one foreign matter.

Method of manufacturing a regenerated cellulosic molded body, wherein the method comprises supplying a starting material which comprises cellulose and at least one foreign matter, transferring at least a part of the starting material with at least a part of the at least one foreign matter into a spinning mass which additionally contains a solvent for solving at least a part of the cellulose of the starting material in the solvent, and extruding the spinning mass to the molded body, and subsequently precipitating in a spinning bath, wherein thereby the molded body is obtained, wherein the molded body comprises cellulose and at least a part of the at least one foreign matter.

Method of recycling a textile material which comprises cellulose for manufacturing regenerated cellulosic molded bodies, wherein in the method the textile material is comminuted, at least a part of non-fiber-constituents of the comminuted textile material is separated from fiber-constituents of the comminuted textile material, at least a part of non-cellulosic fibers of the fiber-constituents is mechanically separated from cellulosic fibers of the fiber-constituents, at least a further part of the non-cellulosic fibers is chemically separated from the cellulosic fibers, and the molded bodies are generated based on the cellulosic fibers after mechanically separating and chemically separating.