D06M2101/06

FABRIC COMPOSITIONS COMPRISING ATTACHED ASCORBIC ACID

The invention relates to antimicrobial and/or antiviral fabric compositions comprising ascorbic acid, citric acid, sodium hypophosphite, or a mixture thereof. The ascorbic acid may be covalently attached to at least one cellulosic portion of the fabric composition. The invention also relates to methods for preparing such fabric compositions.

ANTIBACTERIAL TEXTILE AND PREPARATION METHOD THEREOF

An antibacterial textile and a preparation method thereof are provided. The antibacterial textile provides advantages as followings: various sources for raw material ingredients; low cost and good antibacterial effect; safe and eco-friendly; simple in preparation method; and easy operation. Therefore, the present invention is widely applicable in industrial production.

PAD-DRY CATIONIZATION OF TEXTILES
20230071562 · 2023-03-09 ·

Described are methods and systems for cationizing and dyeing a natural fiber-containing textile, which uses a mono- or di-quaternized cationizing agent. The method includes a step of heating the textile to a temperature in the range of 90° C. to less than 110° C. for a period of time in the range of 1 min to 10 min to react the cationizing agent with the textile. The cationization step in the presence of heat using the halogenated cationization agent of the invention facilitates improved dyeing.

FABRIC HAVING TOBACCO ENTANGLED WITH STRUCTURAL FIBERS

A smokeless tobacco product includes smokeless tobacco and structural fibers. The structural fibers forming a network in which the smokeless tobacco is entangled. The structural fibers have a composition different from the smokeless tobacco. The tobacco-entangled fabric can have an overall oven volatiles content of at least 10 weight percent. In some embodiments, the structural fibers form a nonwoven network. In some embodiments, fibrous structures of the smokeless tobacco are entangled with the structural fibers.

Wearable triboelectric generator for energy harvesting

The present disclosure relates to a wearable water triboelectric generator, wherein the water triboelectric generator comprises a first substrate having a first surface and a second surface, wherein the first surface and the second surface are opposing to each other; and wherein the first surface comprises a modified hydrophobic surface comprising a coating of hydrophobic cellulose oleoyl ester nanoparticles. There is also provided a wearable dual mode water and contact triboelectric generator comprising said water triboelectric generator and a contact triboelectric generator, wherein the water triboelectric generator and the contact triboelectric generator are arranged such that the first substrate of the water triboelectric generator completely surrounds or encapsulates the contact triboelectric generator.

Fine cellulose fiber, production method thereof, slurry, and composite

Provided are: a fine cellulose fiber that is superior in handling properties and that can suitably be used as a reinforcing material or the like for resin; a production method of the fine cellulose fiber; and a slurry and a composite comprising the fine cellulose fibers. The present invention pertains to fine cellulose fibers comprising a carbamate group. The degree of substitution with the carbamate group with respect to hydroxy groups in the fine cellulose fibers is preferably no less than 0.05 and no greater than 0.5. The present invention pertains to a slurry comprising the fine cellulose fibers, to a composite comprising the fine cellulose fibers and a resin, and to a production method of the fine cellulose fibers, comprising performing a heat treatment on a mixture of a plant raw material and urea or the like, and performing a miniaturization treatment of the plant raw material.

ONE STAGE METHOD FOR ACID METAL REMOVAL AND BLEACH

There is provided a process for chemically pretreating reclaimed cellulose fibres to be used in the production of moulded bodies from regenerated cellulose, wherein the pretreatment includes one stage, in which stage acid metal removal and acid oxidative bleaching are carried out together. Advantages include that the propensity of the regenerated cellulose to clog when flowing in a tube and through a nozzle is reduced. This is believed to be an effect of an efficient metal removal. The need for additional bleaching steps and/or metal removing steps is reduced or even eliminated. A one-stage method is more efficient, faster and less costly compared to a multi-stage method according to the prior art. From an environmental perspective, acidic metal removal is preferred over removal by chelating agents such as EDTA.

BIOFABRICATION AND MICROBIAL CELLULOSE BIOTEXTILE

A biomaterial may be produced by employing bacterial nanocellulose which are biologically functional and can be enhanced via an enzyme tanning treatment, to form a functional biotextile that has improved functionality and various desirable and/or enhanced properties.

USE OF AQUEOUS DISPERSIONS OF MAGNESIUM COMPOUNDS FOR FUNCTIONAL FINISHING OF TEXTILES

This invention provides a composition and aqueous dispersion comprising magnesium oxide, as a sole active agent or in combination with ammonium phosphate/ammonium polyphosphate for imparting anti-bacterial and/or anti-viral properties to textile products. The present invention further provides methods for preparing such compositions and aqueous dispersions and methods of using the same for textile finishing.

Method for manufacturing a dye scavenging substrate

A method for manufacturing a dye scavenging substrate which comprises the steps of: (a) providing an absorbent substrate; (b) passing the substrate through a bath containing an alkaline solution of a dye scavenging compound selected from: (i) a N-trisubstituted ammonium-2-hydroxy-3-halopropyl compound having the general formula (I), or (ii) a salt of epoxy propyl ammonium having the general formula (II), or a combination thereof; (c) subjecting the substrate to a pressure of from about 0.04 MPa to about 0.40 MPa; (d) wrapping the substrate in a water impermeable material and rotating the substrate for a period of from about 12 hours to about 60 hours; (e) removing the water impermeable material and passing the substrate through a bath containing an acid solution; (f) subjecting the substrate to a pressure of from about 0.15 MPa to about 0.40 MPa; and (g) drying the substrate.