A method for manufacturing a deodorant and antibacterial high-strength protective cloth includes: providing a first fiber thread and a second fiber thread, where the first fiber thread is a core-spun yarn formed by a blended slurry, a nano metal solution, a plurality of inorganic particles, and a plurality of thermoplastic polyurethane colloidal particles, the thermoplastic polyurethane colloidal particles are hot melted and then wrapped around a peripheral side of a core thread of the core-spun yarn for isolation from an outer wrapping layer of the core-spun yarn, and the second fiber thread is the same as the first fiber thread or is a single-thread yarn formed by the blended slurry and the nano metal solution; and intersecting and laminating the first fiber thread and the second fiber thread to form a plurality of bonding layers.

A composite filament includes a core particle comprising a styrene/acrylate polymer resin, and a shell comprising a styrene/acrylate ionomer resin, wherein the styrene/acrylate ionomer resin comprises a metal ion acrylate monomer, and methods of making thereof. Various articles can be manufactured from such composite filaments.

A fabric delivers active ingredients to a surface when the fabric includes a moist-vapor porous combination of fabric materials, and the fabric comprises at least 0.5% by total weight of at least one layer of the fabric of a superabsorbent polymer fiber. The superabsorbent polymer fiber contains an absorbed aqueous reservoir of an aqueous solution carrying the active ingredients. The superabsorbent fiber has a coating on its surface of an aqueous penetrable layer through which a liquid in the absorbed aqueous reservoir can migrate or flow, carrying the active ingredients onto an exposed surface of the superabsorbent polymer fiber, so that the active ingredients on the surface of the superabsorbent polymer can react or interact with an environment in contact with the active ingredients on the superabsorbent polymer fiber surface.

This invention discloses method for feeding Hermetia illucens and used as for preparing composite material of puparium, which comprises the following steps: S1, dry Hermetia illucens pupariums and grind them into powdery, S2, adding powdery of Hermetia illucens pupariums into sodium hydroxide aqueous solution, stirring, separating and filtering, S3, adding the pupariums into hydrochloric acid solution, stirring, separating and filtering; S4, placing the pupariums into sodium hydroxide aqueous solution, stirring, separating and filtering; S5, drying the pupariums, and screening out the granular pretreated powder of the Hermetia illucens pupariums. The invention also disclose preparation method of composite material and thin film of Hermetia illucens pupariums and antibacterial and antimildew additive. The method can effectively improve the yield of chitosan in Hermetia illucens pupariums, and the prepared pupariums powder can be used for preparing polymer composite fibers and thin films of the Hermetia illucens pupariums, thus, the antibacterial effect is greatly improved. A new antibacterial and antimycotic additive can be obtained by compounding the powder of Hermetia illucens pupariums with the powder of oyster shell.

A plant-based functional polyester filament and a preparation method of the plant-based functional polyester filament are provided. The plant-based functional polyester filament includes polyester, and plant extract in a weight percentage range of approximately 0.1%-1.5%. The plant extract includes one or more of a peppermint extract, a valerian extract, a lavender extract, a wormwood extract, a chitin extract and a seaweed extract. The method includes preparing a plant-based functional polyester masterbatch, including: heating polyethylene terephthalate (PET) chips to a molten state, adding an antioxidant and a dispersant to the molten PET, stirring the molten PET, adding a protective agent and a plant extract to the molten PET, stirring the molten PET at a high speed, adding a modifier to the molten PET, obtaining a mixture by uniformly mixing the molten PET, and performing an extrusion granulation process on the mixture.

This document presents algae-derived antimicrobial fiber substrates, and a method of making the same. The fiber may be a synthetic fiber, but can also be formed as a cellulosic (e.g., cotton). In various implementations, an algae-derived antimicrobial fiber substrate can be made to have identical properties and characteristics of nylon-6 of nylon 6-6 polymer or the like, and yet contain antimicrobial, anti-viral, and/or flame retardant algal derived substances. Any of various species of red algae, brown algae, blue-green algae, and brown seaweed (marine microalgae and/or macroalgae) are known to contain a high level of sulfated polysaccharides with inherent antimicrobial, antiviral, and flame-retardant properties, and can be used as described herein. Additionally disclosed are algae-derived flexible foams, whether open-cell or closed-cell, with inherent antimicrobial, antiviral, and flame resistant properties. Further, a process of manufacturing is presented wherein the process may include one or more of the steps of: harvesting algae-biomass; sufficiently drying the algae biomass; blending the dried algae biomass with a carrier resin and various foaming ingredients; adding an algal-derived antimicrobial compound selected from various natural sulfated polysaccharides present in brown algae, red algae, and/or certain seaweeds (marine microalgae); and adding a sufficient quantity of dried algae biomass to the formulation to adequately create a fire resistant flexible foam material.

A method for the production of a glassy metal polymer composite is disclosed. The method comprises adding a polymer and a metal to an extruder, wherein the extruder is heated to an extrusion temperature greater than the melting point of the polymer and the melting point of the metal; mixing the metal and the polymer in the extruder for a predefined residence time; and co-extruding the composite from the extruder.

Embodiments of the present disclosure relate to a violacein-polymer composite nanofibrous antimicrobial membrane and a method for manufacturing same, wherein the membrane comprises violacein having antimicrobial efficacy against methicillin-resistant Staphylococcus aureus (MRSA) caused by resistance to antibiotics and is formed such that one-dimensional nanofibers are three-dimensionally entangled, and can be used as an antimicrobial membrane for preventing and treating MRSA infections. Specifically, a solution in which violacein is uniformly mixed is prepared by dissolving a large amount of violacein in a solution with a polymer dissolved therein, and the solution is subjected to an electrospinning process to synthesize a nanofibrous membrane in which violacein is uniformly included inside/outside nanofibers without agglomeration. Thus, this is different from existing methods for applying a material to the surface of fibers.

The present disclosure relates to polymer resins, fibers, and yarns with permanent antimicrobial activity, and a method of producing the same. In one embodiment, the antimicrobial polymer resin comprises a polymer having less than 2500 ppm of zinc dispersed within the polymer, less than 1000 ppm of phosphorus, wherein the weight ratio of zinc to phosphorus is at least 1.3:1 or less than 0.64:1.

A preparation method of fibers for medical antibacterial fabric includes cooling an antibacterial polyester melt by ring-blowing after extruded from a trilobal spinneret hole on a spinneret, and manufacturing a fully drawn yarn (FDY), then performing a relaxation heat treatment to obtain the fiber. The shapes and sizes of three leaves from different trilobal spinneret holes are the same; wherein all the trilobal spinneret holes are distributed in concentric circles, and the direction of the shortest leaf in each trilobal spinneret hole is randomly distributed. The prepared fiber has a three-dimensional crimp shape and includes antibacterial polyester monofilaments with trilobal cross-section. The fiber has mechanical performance indices as a crimp shrinkage of 26-29%, a crimp stability of 78-82%, a shrinkage elongation of 55-62%, a crimp elastic recovery rate of 70-75%, a breaking strength of 2.4-2.6 cN/dtex, an elongation at break of 55.0±5.0%, and a monofilament fineness of 1.00-1.50 dtex.