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 s-1 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.

Methods and systems for treating cotton yarn are provided. Cotton yarn is partially dissolved by applying a cold aqueous alkaline solvent, rinsing the partially dissolved cotton yarn in water and drying the cotton yarn. Temperature of the solvent and time of exposure to the solvent greatly affect the improved mechanical properties of the cotton yarn.

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.

An object of the present invention is to provide a method for producing protein spinning capable of securing a stable strength by securing sufficient interlacing between fibers. The method for producing a protein spun yarn of the present invention includes a step (a) of preparing a raw material spun yarn including an uncrimped artificial fibroin fiber containing modified fibroin and a step (b) of bringing the raw material spun yarn into contact with an aqueous medium to crimp the artificial fibroin fiber.

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 present invention provides for a process for reducing the content of one or more residuals in aramid fibers or filaments, comprising, in this order, the steps of introducing the aramid fiber or filaments into a extraction solution adjusted to a pH ranging from of 2 to 7, adjusting the extraction solution and the aramid fibers or filaments to a temperature of to from 80 C. to 140 C., removing the aramid fibers or filaments from the extraction solution, introducing the aramid fiber or filaments into a first rinsing solution adjusted to a pH ranging from of 2 to 7, optionally comprising a detergent, adjusting the first rinsing solution and the aramid fibers and filaments to a temperature of from 70 C. to 100 C., removing the aramid fibers or filaments from the first rinsing solution.

A welded yarn may have a cross section about a plane that is perpendicular to the longitudinal axis of the welded yarn wherein the cross-sectional area is comprised of two or more distinct portions, wherein the degree of welding in each portion is different, which May also result in different fiber volume ratios compared to raw yarn substrates.

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.

The present invention relates to a fire protection composite, which is made of a liquid applied coating and a mat or fleece; a process for preparing the fire protection composite; use of the fire protection composite for electric vehicle battery; an electric vehicle battery containing the fire protection composite; and a process for preparing the electric vehicle battery.

A coated microfibrous web, a method for producing the same, the use thereof as a covering of a radiation protection material, and a radiation protection device are described. The coated microfibrous web contains: (i) a microfibrous web containing one or more polyesters and/or one or more polyamides and/or one or more polyamide-polyester copolymers and having an impregnation composition containing (a) an aromatic dicarboxylic acid, the dicarboxylic groups of which are each esterified with a diol, and/or (b) one or more oligomers, each containing 2 to 10 repeat units consisting of a monoester of an aromatic dicarboxylic acid impregnated with a diol; and (ii) a layer comprising polyurethane which is present only on one side of the microfibrous web.