The invention relates to a method for producing an antimicrobial fabric or yarn, said method comprising the steps of immersing a fabric or yarn in an aqueous solution of a metal salt whilst simultaneously subjecting said solution to ultrasonic radiation; and removing the fabric or yarn from said solution and subsequently converting the metal salt in situ in the fabric or yarn into metal oxide nanoparticles, preferably via chemical and heat treatment. Fabrics and yarns obtained or obtainable by such method are also provided. In a further aspect the invention provides an apparatus for performing such method.

The invention relates to a method for producing an antimicrobial fabric or yarn, said method comprising the steps of immersing a fabric or yarn in an aqueous solution of a metal salt whilst simultaneously subjecting said solution to ultrasonic radiation; and removing the fabric or yarn from said solution and subsequently converting the metal salt in situ in the fabric or yarn into metal oxide nanoparticles, preferably via chemical and heat treatment. Fabrics and yarns obtained or obtainable by such method are also provided. In a further aspect the invention provides an apparatus for performing such method.

A process for forming a splittable fiber having the steps of providing a multicomponent fiber; or a multicomponent staple fiber, providing a finish material, and at least partially coating the multicomponent fiber with the finish material to form a splittable fiber. The multicomponent fiber; or a multicomponent staple fiber, contains a first thermoplastic segment comprising polymer component A and a second thermoplastic segment comprising polymer component B. The finish material has an evaporation point of less than about 160° C. A process for forming a nonwoven fabric, a split multicomponent fiber, a split multicomponent fiber with a durable charge, a nonwoven fabric, and a filter and/or a spun yarn formed by the fibers herein is also described.

A process for forming a splittable fiber having the steps of providing a multicomponent fiber; or a multicomponent staple fiber, providing a finish material, and at least partially coating the multicomponent fiber with the finish material to form a splittable fiber. The multicomponent fiber; or a multicomponent staple fiber, contains a first thermoplastic segment comprising polymer component A and a second thermoplastic segment comprising polymer component B. The finish material has an evaporation point of less than about 160° C. A process for forming a nonwoven fabric, a split multicomponent fiber, a split multicomponent fiber with a durable charge, a nonwoven fabric, and a filter and/or a spun yarn formed by the fibers herein is also described.

The application of melanin to fabric improves resistance to chemical pass-through, with possible application in protective garments, shelters, and filtration materials.

The application of melanin to fabric improves resistance to chemical pass-through, with possible application in protective garments, shelters, and filtration materials.

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.

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.

A flame-retardant ultraviolet-resistant aramid fiber, the preparation method therefor comprising the following steps: adding nanoparticles into a hydrogen peroxide solution, performing magnetic stirring for 0.5-1 h, adding a sulfuric acid solution, and further performing magnetic stirring for 0.5 h; performing filtering to obtain a filter cake, and washing the filter cake with water and drying same to obtain modified particles; modifying the modified particles with curcumin and dopamine to obtain organic substance-modified particles; and finally subjecting the organic substance-modified particles to a reaction with a siliconmethoxylated aramid fiber, so as to obtain a surface-modified aramid fiber. The present invention has high ultraviolet absorption and extremely low catalytic activity, avoiding damage to a fiber structure by photocatalysis in a radiation process, and in particular improving flame retardancy of the aramid fiber.

A flame-retardant ultraviolet-resistant aramid fiber, the preparation method therefor comprising the following steps: adding nanoparticles into a hydrogen peroxide solution, performing magnetic stirring for 0.5-1 h, adding a sulfuric acid solution, and further performing magnetic stirring for 0.5 h; performing filtering to obtain a filter cake, and washing the filter cake with water and drying same to obtain modified particles; modifying the modified particles with curcumin and dopamine to obtain organic substance-modified particles; and finally subjecting the organic substance-modified particles to a reaction with a siliconmethoxylated aramid fiber, so as to obtain a surface-modified aramid fiber. The present invention has high ultraviolet absorption and extremely low catalytic activity, avoiding damage to a fiber structure by photocatalysis in a radiation process, and in particular improving flame retardancy of the aramid fiber.