Compositions that include a polymer and an aldaric acid, such as glucaric acid, are disclosed. The compositions may include polyvinyl alcohol and glucaric acid. The compositions may also include polyacrylonitrile and glucaric acid. In addition, the compositions may further include lignin. Also disclosed are fibers including the compositions, methods of making the fibers, and uses of the fibers.

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).

The present disclosure relates generally to carbon fibers having high tensile strength and modulus of elasticity, as well as a process for the manufacture of such carbon fiber. The process comprises spinning a polymer/solvent solution into a solvent/water bath in the range of 78%-85% solvent, thereby producing a dense fiber structure, and subsequently carbonizing the polymer precursor fiber at a lower than typical carbonization temperature to form carbon fibers.

The present disclosure relates generally to carbon fibers having high tensile strength and modulus of elasticity, as well as a process for the manufacture of such carbon fiber. The process comprises spinning a polymer/solvent solution into a solvent/water bath in the range of 78%-85% solvent, thereby producing a dense fiber structure, and subsequently carbonizing the polymer precursor fiber at a lower than typical carbonization temperature to form carbon fibers.

A spinning nozzle which has a perforated part in which ejection holes have been arranged in a density as high as 600-1,200 holes/mm.sup.2. This process for producing a fibrous bundle comprises ejecting a spinning dope having a viscosity as measured at 50° C. of 30-200 P from the ejection holes of the spinning nozzle to produce a fibrous bundle. This fibrous bundle has a single-fiber fineness of 0.005-0.01 dtex. By the wet-process direct spinning, a mass of nanofibers which are stably uniform and continuous can be produced at a high efficiency.

A spinning nozzle which has a perforated part in which ejection holes have been arranged in a density as high as 600-1,200 holes/mm.sup.2. This process for producing a fibrous bundle comprises ejecting a spinning dope having a viscosity as measured at 50° C. of 30-200 P from the ejection holes of the spinning nozzle to produce a fibrous bundle. This fibrous bundle has a single-fiber fineness of 0.005-0.01 dtex. By the wet-process direct spinning, a mass of nanofibers which are stably uniform and continuous can be produced at a high efficiency.

Provided is a dental cord using a nanofiber multiple yarn having a large specific surface area and a large number of three-dimensional pores, thereby effectively impregnating a drug such as a hemostatic agent, and a method of manufacturing the dental cord. The dental cord includes: a nanofiber multiple yarn which is obtained by plying and twisting at least two nanofiber tape yarns and which is impregnated with a drug, wherein the at least two nanofiber tape yarns are integrated by nanofibers made of fiber moldability polymer materials and having an average diameter of less than 1 μm, to thus be formed of a nanofiber web having three-dimensional micropores.

A metal adsorption acrylic fiber wherein the strontium adsorption rate is 85% or more when the strontium adsorption rate is measured using the following measurement method. A strontium adsorption rate measurement method (strontium 0.1 ppm measurement method) involves immersing a metal adsorption acrylic fiber into an immersion fluid, collecting the immersion fluid as a testing solution 24 hours after beginning the immersion, analyzing the quantity of strontium in the testing solution, obtaining the concentration (C.sub.1) (ppm) of strontium in the testing solution, creating a contrast solution, analyzing the quantity of strontium in the contrast solution as in the case with the testing solution, obtaining the concentration (C.sub.2) (ppm) of strontium in the contrast solution, and calculating the strontium adsorption rate of the metal adsorption acrylic fiber by using the following equation: strontium adsorption rate (%)={(C.sub.2−C.sub.1)/C.sub.2}×100.

A metal adsorption acrylic fiber wherein the strontium adsorption rate is 85% or more when the strontium adsorption rate is measured using the following measurement method. A strontium adsorption rate measurement method (strontium 0.1 ppm measurement method) involves immersing a metal adsorption acrylic fiber into an immersion fluid, collecting the immersion fluid as a testing solution 24 hours after beginning the immersion, analyzing the quantity of strontium in the testing solution, obtaining the concentration (C.sub.1) (ppm) of strontium in the testing solution, creating a contrast solution, analyzing the quantity of strontium in the contrast solution as in the case with the testing solution, obtaining the concentration (C.sub.2) (ppm) of strontium in the contrast solution, and calculating the strontium adsorption rate of the metal adsorption acrylic fiber by using the following equation: strontium adsorption rate (%)={(C.sub.2−C.sub.1)/C.sub.2}×100.

The invention relates to a method for the production of thermally stabilised melt spun fibres, in which polyacrylonitrile (PAN) fibres or PAN fibre precursors produced by melt spinning are treated in an aqueous alkaline solution which comprises in addition a solvent for PAN. Likewise, the invention relates to fibres which are producible according to this method.