Patent classifications
D06M14/04
CONTROLLABLE LIQUID TRANSPORT MATERIAL, SYSTEM, AND METHOD FOR PREPARING THEREOF
Provided herein are a controllable liquid transport material, a controllable liquid transport system and a method for preparing a controllable liquid transport material, where a first region of the controllable liquid transport material is treated to be hydrophobic, while a plurality of second regions partially contacted or completely separated with different shapes are treated to have a gradient or varied wettabilities and/or pore sizes for passively controllable liquid transport, and/or integrated with a smart material for actively controllable liquid transport driven by an external force, allowing efficiently and controllably directional transport of a liquid e.g., sweat. The controllable liquid transport system comprises a controllable liquid transport material used as a liquid transport layer and a breathable, waterproof protective layer.
CONTROLLABLE LIQUID TRANSPORT MATERIAL, SYSTEM, AND METHOD FOR PREPARING THEREOF
Provided herein are a controllable liquid transport material, a controllable liquid transport system and a method for preparing a controllable liquid transport material, where a first region of the controllable liquid transport material is treated to be hydrophobic, while a plurality of second regions partially contacted or completely separated with different shapes are treated to have a gradient or varied wettabilities and/or pore sizes for passively controllable liquid transport, and/or integrated with a smart material for actively controllable liquid transport driven by an external force, allowing efficiently and controllably directional transport of a liquid e.g., sweat. The controllable liquid transport system comprises a controllable liquid transport material used as a liquid transport layer and a breathable, waterproof protective layer.
CELLULOSE FIBER COMPOSITE
The invention relates to [1] a cellulose fiber composite excellent in dispersion stability, in which at least one amine selected from a polyamine and a monoamine having a reactive functional group bonds to anion-modified cellulose fibers, and which satisfies at least one of amine introduction ratio of 60% or less (requirement 1) and average polymerization degree of anion-modified cellulose fibers of 300 or less (requirement 2), [2] a dispersion in which the cellulose fiber composite is dispersed in a medium, [3] a resin composition produced by blending the cellulose fiber composite and a resin, [4] a molded article produced by molding the cellulose fiber composite or the resin composition, and [5] a method for producing the cellulose fiber composite.
Metallic textiles for flexible wearable lithium ion batteries
This disclosure provides a method for preparing a current collector. The method includes: (1) anchoring vinyl groups onto the surface of textiles through the silanization between hydroxyl groups and coupling agents; (2) synthesizing polyelectrolyte brushes through in-situ radical polymerization; and (3) obtaining catalyst ions on the polyelectrolyte brushes through ion-exchange and obtaining metal-coated layers through subsequent electroless deposition). The current collector according to the present disclosure has high electrical conductivity and excellent mechanical flexibility, and thus the lithium ion battery including the same is suitable for portable and wearable electronic devices.
METHOD OF MANUFACTURING CUSHIONING MATERIAL, AND CUSHIONING MATERIAL
A method of manufacturing a cushioning material P includes a defibrating step of defibrating a cloth to produce fibers F in dry forming, a mixing step of mixing the fibers F with a bonding agent to produce a mixture, an accumulation step of accumulating the mixture in air to produce a web W, and a first forming step of pressurizing and heating the web W to form the web W.
METHOD OF MANUFACTURING CUSHIONING MATERIAL, AND CUSHIONING MATERIAL
A method of manufacturing a cushioning material P includes a defibrating step of defibrating a cloth to produce fibers F in dry forming, a mixing step of mixing the fibers F with a bonding agent to produce a mixture, an accumulation step of accumulating the mixture in air to produce a web W, and a first forming step of pressurizing and heating the web W to form the web W.
WATER-REPELLENT FABRIC AND PREPARATION METHOD THEREFOR
Disclosed are a water-repellent fabric and a preparation method therefor. A short carbon chain fluoroalkyl alcohol with different fluorine atom numbers used as a starter is firstly treated with an acylation reagent to generate a short carbon chain fluoroalkyl bromoacetate, and is then synthesized with N,N-bis(p-toluenesulfonyl) hydrazine to form a short carbon chain fluoroalkyl diazoacetate monomer, a fabric is respectively treated with an acylation reagent and N,N″-dimethylbenzenesulfonyl hydrazide in sequence to prepare a diazotized fabric having grafting sites on the surface thereof, and finally, a fluorine-containing polymer having a single carbon repeating unit is grafted to the surface of the fabric via a covalent bond by means of carbene polymerization, and thus a hydrophobic modified fabric is prepared. The entire reaction is carried out at a low temperature/room temperature, the operation is simple, and the process is environmentally friendly.
WATER-REPELLENT FABRIC AND PREPARATION METHOD THEREFOR
Disclosed are a water-repellent fabric and a preparation method therefor. A short carbon chain fluoroalkyl alcohol with different fluorine atom numbers used as a starter is firstly treated with an acylation reagent to generate a short carbon chain fluoroalkyl bromoacetate, and is then synthesized with N,N-bis(p-toluenesulfonyl) hydrazine to form a short carbon chain fluoroalkyl diazoacetate monomer, a fabric is respectively treated with an acylation reagent and N,N″-dimethylbenzenesulfonyl hydrazide in sequence to prepare a diazotized fabric having grafting sites on the surface thereof, and finally, a fluorine-containing polymer having a single carbon repeating unit is grafted to the surface of the fabric via a covalent bond by means of carbene polymerization, and thus a hydrophobic modified fabric is prepared. The entire reaction is carried out at a low temperature/room temperature, the operation is simple, and the process is environmentally friendly.
ANILINE ACID ANHYDRIDE, PREPARATION METHOD THEREFOR, AND POLYAMINO ACID-GRAFTED CHAIN
Disclosed are an aniline anhydride, a preparation method therefor, and a polyaminoacid graft chain. In the presence of an acid binding agent, an addition-elimination reaction is carried out between N-phenyl amino acid and Boc anhydride to obtain N-phenyl-Boc-glycine; and under a nitrogen atmosphere, the N-phenyl-Boc-glycine is subject to cyclization to obtain the aniline anhydride. The polyaminoacid graft chain can be obtained using the aniline anhydride disclosed by means of chemical grafting and thus be covalently bonded with fiber. The fastness is high, the wearability of fabric is not affected, and the problem of low fastness of water-repellent fabric obtained by coating is solved. The polyaminoacid graft chain is biocompatible, naturally degradable and environmentally friendly, and is consistent with the current trend of developing green chemicals.
ANILINE ACID ANHYDRIDE, PREPARATION METHOD THEREFOR, AND POLYAMINO ACID-GRAFTED CHAIN
Disclosed are an aniline anhydride, a preparation method therefor, and a polyaminoacid graft chain. In the presence of an acid binding agent, an addition-elimination reaction is carried out between N-phenyl amino acid and Boc anhydride to obtain N-phenyl-Boc-glycine; and under a nitrogen atmosphere, the N-phenyl-Boc-glycine is subject to cyclization to obtain the aniline anhydride. The polyaminoacid graft chain can be obtained using the aniline anhydride disclosed by means of chemical grafting and thus be covalently bonded with fiber. The fastness is high, the wearability of fabric is not affected, and the problem of low fastness of water-repellent fabric obtained by coating is solved. The polyaminoacid graft chain is biocompatible, naturally degradable and environmentally friendly, and is consistent with the current trend of developing green chemicals.