A preparation method of self-crimping elastic combined filament yarns for knitting is disclosed, wherein the combined filament yarns are extruded from the same spinneret; a first fiber-forming polymer melt is divided into two ways, one is directly extruded after distribution; and the other is extruded after distribution by side-by-side composite spinning together with a second fiber-forming polymer melt; the first fiber-forming polymer and the second fiber-forming polymer are compatible or partially compatible; on the same spinneret, a ratio of the number of spinneret holes m for direct extrusion to the number of spinneret holes n for extrusion after distribution by side-by-side composite spinning is 1:(5-10); the self-crimping elastic combined filament yarns for knitting are prepared according to specific spinning processes, wherein the combined filament yarn mainly comprises a first fiber-forming polymer monofilament and a first/second fiber-forming polymer side-by-side composite monofilament; wherein the monofilament crimping directions are randomly distributed.

A preparation method of self-crimping elastic combined filament yarns for knitting is disclosed, wherein the combined filament yarns are extruded from the same spinneret; a first fiber-forming polymer melt is divided into two ways, one is directly extruded after distribution; and the other is extruded after distribution by side-by-side composite spinning together with a second fiber-forming polymer melt; the first fiber-forming polymer and the second fiber-forming polymer are compatible or partially compatible; on the same spinneret, a ratio of the number of spinneret holes m for direct extrusion to the number of spinneret holes n for extrusion after distribution by side-by-side composite spinning is 1:(5-10); the self-crimping elastic combined filament yarns for knitting are prepared according to specific spinning processes, wherein the combined filament yarn mainly comprises a first fiber-forming polymer monofilament and a first/second fiber-forming polymer side-by-side composite monofilament; wherein the monofilament crimping directions are randomly distributed.

The present invention relates to a modified fibroin including a domain sequence represented by Formula 1: [(A).sub.nmotif-REP].sub.m or Formula 2: [(A).sub.nmotif-REP].sub.m−(A).sub.n motif, in which the domain sequence has an amino acid sequence with a reduced content of a glutamine residue equivalent to an amino acid in which one or a plurality of glutamine residues in REP are deleted or substituted with other amino acid residues, as compared with a naturally occurring fibroin.

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.

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.

A nonwoven fabric manufacturing facility includes a fiber assembly manufacturing step and a heating and drawing step. In the fiber assembly manufacturing step, fibers formed using an electrospinning method are collected to form a fiber assembly. In the heating and drawing step, the fiber assembly is drawn to form nonwoven fabric in a state where the fiber assembly is heated to a melting point of the fibers. In the formed nonwoven fabric, an average pore diameter is 15 μm or more, a relative standard deviation of a pore diameter distribution is 0.1 or less, and an average fiber diameter of the fibers is 3 μm or less.

The present invention relates to a method for manufacturing a wholly aromatic liquid-crystalline polyester fiber with enhanced spinnability, and more specifically, to a method for manufacturing a wholly aromatic liquid-crystalline polyester fiber including: pelletizing a resin manufactured by adding 1.08 equivalents to 1.12 equivalents of acetic anhydride to raw material monomers including hydroxy benzoic acid, hydroxy naphthoic acid, biphenol, terephthalic acid, and isophthalic acid, followed by solid-phase polycondensation, and melt-spinning under oil conditions in which winding-up improving oil is diluted to 0.5% to 2% and silicone spinning oil for high temperature is diluted to 0.5% to 2%, respectively, with water as a solvent.

The present invention relates to a method for manufacturing a wholly aromatic liquid-crystalline polyester fiber with enhanced spinnability, and more specifically, to a method for manufacturing a wholly aromatic liquid-crystalline polyester fiber including: pelletizing a resin manufactured by adding 1.08 equivalents to 1.12 equivalents of acetic anhydride to raw material monomers including hydroxy benzoic acid, hydroxy naphthoic acid, biphenol, terephthalic acid, and isophthalic acid, followed by solid-phase polycondensation, and melt-spinning under oil conditions in which winding-up improving oil is diluted to 0.5% to 2% and silicone spinning oil for high temperature is diluted to 0.5% to 2%, respectively, with water as a solvent.

Provided is a method of manufacturing MoS.sub.2 having a 1T crystal structure. The method includes performing phase transition from a 2H crystal structure of MoS.sub.2 to the 1T crystal structure by reacting MoS.sub.2 having the 2H crystal structure with CO gas. The phase transition includes annealing the MoS.sub.2 having the 2H crystal structure in an atmosphere including CO gas.

Disclosed in the present invention is a polyamide 5X industrial yarn. The polyamide 5X industrial yarn has a heat-resistant break strength retention rate of 90% or more after being treated at 180° C. for 4 hrs; a heat-resistant break strength retention rate of 90% or more after being treated at 230° C. for 30 mins; and a dry heat shrinkage of 8.0% or less. The polyamide 5X industrial yarn is widely used in the fields of sewing threads, tire cords, air bag yarns, release cloth, krama, canvas, safety belts, ropes, fishing nets, industrial filter cloth, conveyor belts, parachutes, tents, bags and suitcases.