Expanded, nanofiber structures are provided as well as methods of use thereof and methods of making.

The present invention relates to a liquid-state temporary reinforcing material, a preparation method therefor and an application thereof. The liquid-state temporary reinforcing material comprises a reinforcing material and a crystallization inhibitor; the reinforcing material is selected from molecules of any two or more of menthol, menthone, menthol ester and menthol ether, and the content of the crystallization inhibitor is less than 50 ppm. For the liquid-state temporary reinforcing material of the present invention, the menthol and the derivatives of the liquid-state temporary reinforcing material are integrally mixed together to form the composite material for temporary reinforcing, the composite material being liquid and volatilization-controllable at room temperature. Thus, the temporary reinforcing requirements for extracting cultural relics at an archaeology excavation site may be met, and the material is convenient to use.

A welding process may be configured to convert a substrate comprised of short staple fibers into a welded substrate having significantly increased strength as compared to the raw substrate. When applied to a one-dimensional substrate, such as a yarn, the welding process may also reduce the diameter of the welded substrate compared to that of the raw substrate. Additionally, the welding process may be configured to impart superior color properties to the welded substrate compared to the color properties of the raw substrate, which superior color properties may be very pronounced when performing a welding process on a raw substrate comprised of colored and/or dyed recycled fibers.

A dyeing and welding process may be configured to convert a substrate into a welded substrate having at least some color imparted thereto via a dye and/or coloring agent by applying a process solvent having a dye and/or coloring agent therein to the substrate, wherein the process solvent interrupts one or more intermolecular force between one or more component in the substrate. The substrate may be configured as a natural fiber, such as cellulose, hemicelluloses, and silk. The process solvent may include a binder, such as dissolved biopolymer (e.g., cellulose). After application of a process solvent comprised of a dye and/or coloring agent, the substrate may be exposed to a second application of a process solvent comprised of a binder, which second application may occur before or after a process temperature/pressure zone, process solvent recovery zone, and/or drying zone.

A process is disclosed for modifying citrus fiber. Citrus fiber is obtained having a c* close packing concentration value of less than 3.8 w %, anhydrous basis. The citrus fiber can have a viscosity of at least 1000 mPa.Math.s, wherein said citrus fiber is dispersed in standardized water at a mixing speed of from 800 rpm to 1000 rpm, to a 3 w/w % citrus fiber/standardized water solution, and wherein said viscosity is measured at a shear rate of 5 s1 at 20 C. Citrus fiber can be obtained having a CIELAB L* value of at least 90. The citrus fiber can be used in food products, feed products, beverages, personal care products, pharmaceutical products or detergent products.

Disclosed is a method for mass-producing densified carbon nanotube fiber. The method includes preparing carbon nanotube fiber, swelling the carbon nanotube fiber by applying an acid solution thereto, and stretching the carbon nanotube fiber, coagulating the stretched carbon nanotube fiber so as to remove the acid solution present therein, and drying the coagulated carbon nanotube fiber.

The present invention relates to a surface-modified aramid fiber and a method for preparing the same. The method includes the following steps: modifying an aramid fiber having amino groups and carboxyl groups on the surface with siloxane -glycidoxypropyltrimethoxysilane to obtain a silicon methoxylated aramid fiber; reacting same with a cerium oxide coated with polydopamine modified chaotic boron nitride to obtain a surface-modified aramid fiber. The cerium oxide coated with polydopamine modified chaotic boron nitride has high ultraviolet absorption, and has extremely low catalytic activity, avoiding the damage to a fiber structure by photocatalysis during radiation, being an effective, safe and highly-efficient ultraviolet absorber. The surface-modified aramid fiber provided in the present invention has an ultraviolet-resistant function, high surface activity, good thermal performance, and better mechanical performance, providing excellent overall performance, and having higher utilization value. The method is simple and controllable, being suitable for large scale production.

A welding process may be configured to convert a substrate into a welded substrate by applying a process solvent to the substrate, wherein the process solvent interrupts one or more intermolecular force between one or more component in the substrate. The substrate may be configured as a natural fiber, such as cellulose, hemicelluloses, and silk. The process solvent may be configured as an ionic-liquid based solvent and the welded substrate may be a congealed network after the process solvent has been adequately swollen and/or mobilized the substrate. A welding process may be configured such that individual fibers of a substrate are not fully dissolved such that material in the fiber core may be left in the native state by controlling process variables. The welding process fibers may have a tenacity 10% or 20% greater or a diameter 25% less than that of a cellulosic-based yarn substrate.

The invention provides devices for removal of moisture. The devices include desiccant contained in the interior of the device and barriers that restrict movement of the desiccant within the interior of the device. The invention also provides wearable apparatuses that include devices for moisture removal.

The present disclosure provides a method for producing a cell-culturing polyvinyl alcohol-based nanofiber structure, the method comprising: electrospinning an electrospun solution to form a nanofiber mat, wherein the electrospun solution contains polyvinyl alcohol (PVA), polyacrylic acid (PA) and glutaraldehyde (GA); crosslinking the nanofiber mat via a hydrochloric acid (HCl) vapor treatment; and treating the crosslinked nanofiber mat with dimethylformamide (DMF) solvent to crystallize the nanofiber mat.