A method of manufacturing a graphene fiber is provided. The method includes preparing a source solution including graphene oxide, supplying the source solution into a coagulation solution to form a graphene oxide fiber, reducing the graphene oxide fiber to form a primary graphene fiber, and Joule-heating the primary graphene fiber to form a secondary graphene fiber.

The present disclosure provides a preparation method of a plasma-treated nanofiber-based hydrogen gas sensing material, including the following steps: (1) stirring a mixed solution of absolute ethanol, polyvinyl pyrrolidone (PVP), N, N-dimethylformamide, SnCl.sub.2.H.sub.2O, and Zn(CH.sub.3COO).sub.2.2H.sub.2O uniformly on a constant-temperature magnetic stirrer to obtain a spinning solution; (2) electrospinning the spinning solution and depositing on an aluminum foil to obtain a spinning fiber; (3) annealing the spinning fiber in a muffle furnace to obtain a hydrogen gas sensing material sample; and (4) subjecting the hydrogen gas sensing material sample to a vacuum argon plasma treatment with a Hall ion source to obtain the nanofiber-based hydrogen gas sensing material. In the method, nanofibers are prepared by electrospinning and subjected to the vacuum argon plasma treatment through the Hall ion source. The prepared sensing material has an extremely large specific surface area, and gas-sensing properties of rapid response and high sensitivity to hydrogen gas.

The present disclosure provides a preparation method of a plasma-treated nanofiber-based hydrogen gas sensing material, including the following steps: (1) stirring a mixed solution of absolute ethanol, polyvinyl pyrrolidone (PVP), N, N-dimethylformamide, SnCl.sub.2.H.sub.2O, and Zn(CH.sub.3COO).sub.2.2H.sub.2O uniformly on a constant-temperature magnetic stirrer to obtain a spinning solution; (2) electrospinning the spinning solution and depositing on an aluminum foil to obtain a spinning fiber; (3) annealing the spinning fiber in a muffle furnace to obtain a hydrogen gas sensing material sample; and (4) subjecting the hydrogen gas sensing material sample to a vacuum argon plasma treatment with a Hall ion source to obtain the nanofiber-based hydrogen gas sensing material. In the method, nanofibers are prepared by electrospinning and subjected to the vacuum argon plasma treatment through the Hall ion source. The prepared sensing material has an extremely large specific surface area, and gas-sensing properties of rapid response and high sensitivity to hydrogen gas.

A high-strength polyamide 610 multifilament has a sulfuric acid relative viscosity of 3.0 to 3.7 and a drying strength of more than 9.2 cN/dtex and within 11.0 cN/dtex, having a total fineness of 100 to 2,500 dtex and a single fiber fineness of 1.5 to 40 detex and a birefringence Δn of 50.0 x 10.sup.-3 or more.

Disclosed are an industrial polyamide yarn, a preparation method therefor, and the use thereof. The raw materials for producing the industrial polyamide yarn include at least 1,5-pentanediamine and a linear aliphatic dibasic acid; or polyamide 5X obtained by the polymerization of 1,5-pentanediamine and a linear aliphatic dibasic acid as monomers. The industrial polyamide yarn according to an embodiment has the characteristics of a low water absorption, a good dimensional stability, a high fracture strength, and a good heat resistance.

The present application discloses a method for preparing microporous PVA fiber comprising the following steps: Step 1: preparing spinning solution, calcium hydroxide solution, and sodium sulfate solution; Step 2: cooling the spinning solution to 40-60° C., and adding a foaming agent thereto to provide the PVA spinning stock solution; Step 3: spinning into the sodium sulfate solution so that the fiber containing the reaction product of the foaming agent and the mirabilite is dehydrated to provide a primary PVA fiber; Step 4: reacting the fiber with the calcium hydroxide solution to provide a secondary fiber; Step 5: foaming and pore forming; and Step 6: cleaning and drying to provide the final product of microporous PVA fiber.

The present application discloses a method for preparing microporous PVA fiber comprising the following steps: Step 1: preparing spinning solution, calcium hydroxide solution, and sodium sulfate solution; Step 2: cooling the spinning solution to 40-60° C., and adding a foaming agent thereto to provide the PVA spinning stock solution; Step 3: spinning into the sodium sulfate solution so that the fiber containing the reaction product of the foaming agent and the mirabilite is dehydrated to provide a primary PVA fiber; Step 4: reacting the fiber with the calcium hydroxide solution to provide a secondary fiber; Step 5: foaming and pore forming; and Step 6: cleaning and drying to provide the final product of microporous PVA fiber.

A thermal-moisture comfortable polyester FDY for summer use and a preparation method thereof are provided. The FDY is made of matting agents dispersed polyester via the steps of spinning melt metering, extruding via the compositional spinneret, cooling, oiling, drawing, heat setting and winding. The woven fabrics manufactured with the FDY possess a wicking height and an evaporation rate of larger than or equal to 135 mm and 0.22 g/h, respectively. The compositional spinneret is simultaneously provided with cruciform orifices and circular orifices, and the length ratio of cruciform orifice to circular orifice is equal to the product of their equivalent diameter ratio and a coefficient K, here equivalent diameter is the ratio of orifice cross-section area to its circumference and K ranges from 0.97 to 1.03, and the oiling involves the oiling agent containing 67.30-85.58 wt % of crown ether.

A thermal-moisture comfortable polyester FDY for summer use and a preparation method thereof are provided. The FDY is made of matting agents dispersed polyester via the steps of spinning melt metering, extruding via the compositional spinneret, cooling, oiling, drawing, heat setting and winding. The woven fabrics manufactured with the FDY possess a wicking height and an evaporation rate of larger than or equal to 135 mm and 0.22 g/h, respectively. The compositional spinneret is simultaneously provided with cruciform orifices and circular orifices, and the length ratio of cruciform orifice to circular orifice is equal to the product of their equivalent diameter ratio and a coefficient K, here equivalent diameter is the ratio of orifice cross-section area to its circumference and K ranges from 0.97 to 1.03, and the oiling involves the oiling agent containing 67.30-85.58 wt % of crown ether.

Hybrid carbon nanofiber (Cnf) products (e.g., mats, yarns, webs, etc.) and methods of fabricating the same are provided. The hybrid Cnf products are flexible and lightweight and have high thermal conductivity. An electrospinning process can be used to fabricate the hybrid Cnf products and can include preparation of an electrospinning solution, electrospinning, and carbonization (e.g., under a vacuum condition).