D01F6/04

Method to fabricate glassy-metal polymer composites

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.

Polymeric materials and articles manufactured there from

A method for manufacturing a three dimensional object includes steps of: providing a digital description of the object as a set of voxels; sequentially creating an actual set of voxels corresponding to the digital set of voxels. At least one voxel comprises a polymer derived from: polyol and an ionic monomer. The calculated charge density of the resulting polymer is 0.01 to 0.7 mEq/g. A three-dimensional object having at least one voxel. The at least one voxel including a polymer derived from: a polyol and an ionic monomer, and the calculated charge density of the resulting polymer is 0.01 to 0.7 mEq/g.

Polymeric materials and articles manufactured there from

A method for manufacturing a three dimensional object includes steps of: providing a digital description of the object as a set of voxels; sequentially creating an actual set of voxels corresponding to the digital set of voxels. At least one voxel comprises a polymer derived from: polyol and an ionic monomer. The calculated charge density of the resulting polymer is 0.01 to 0.7 mEq/g. A three-dimensional object having at least one voxel. The at least one voxel including a polymer derived from: a polyol and an ionic monomer, and the calculated charge density of the resulting polymer is 0.01 to 0.7 mEq/g.

Ultra-high molecular weight, ultra-fine particle size polyethylene, preparation method therefor and use thereof

An ultra-high molecular weight, ultra-fine particle size polyethylene has a viscosity average molecular weight (Mv) greater than 1×10.sup.6. The polyethylene is spherical or are sphere-like particles having a mean particle size of 10-100 μm, having a standard deviation of 2-15 μm and a bulk density of 0.1-0.3 g/mL. Using the polyethylene as a basic polyethylene, a grafted polyethylene can be obtained by means of a solid-phase grafting method; and a glass fiber-reinforced polyethylene composition comprising the polyethylene and glass fibers, and a sheet or pipe prepared therefrom; a solubilized ultra-high molecular weight, ultra-fine particle size polyethylene; and a fiber and a film prepared from the solubilized ultra-high molecular weight, ultra-fine particle size polyethylene may also be obtained. The method has simple steps, is easy to control, has a relatively low cost and a high repeatability, and can realize industrialisation.

SKIN COOLING FABRIC, POLYETHYLENE YARN THEREFOR, AND METHOD FOR MANUFACTURING POLYETHYLENE YARN

Disclosed is a skin cooling fabric that can provide a user with a soft tactile sensation as well as a cooling feeling or a cooling sensation, a polyethylene yarn having improved weavability, and a method for manufacturing the yarn. The skin cooling fabric of the present invention includes a plurality of weft yarns, and a plurality of warp yarns, wherein each of the weft yarns and warp yarns has a tensile strength of 3.5 to 8.5 g/de, a tensile modulus of 15 to 80 g/de, elongation at break of 14 to 55%, and crystallinity of 55 to 85%.

SKIN COOLING FABRIC, POLYETHYLENE YARN THEREFOR, AND METHOD FOR MANUFACTURING POLYETHYLENE YARN

Disclosed is a skin cooling fabric that can provide a user with a soft tactile sensation as well as a cooling feeling or a cooling sensation, a polyethylene yarn having improved weavability, and a method for manufacturing the yarn. The skin cooling fabric of the present invention includes a plurality of weft yarns, and a plurality of warp yarns, wherein each of the weft yarns and warp yarns has a tensile strength of 3.5 to 8.5 g/de, a tensile modulus of 15 to 80 g/de, elongation at break of 14 to 55%, and crystallinity of 55 to 85%.

POLYETHYLENE YARN OF HIGH TENACITY HAVING HIGH DIMENSIONAL STABILITY AND METHOD FOR MANUFACTURING THE SAME
20220364273 · 2022-11-17 ·

The present disclosure relates to a polyethylene yarn and a method for manufacturing the same. In the present disclosure, there are provided a polyethylene yarn having excellent dimensional stability and high tenacity, and a method for manufacturing the above polyethylene yarn more efficiently.

POLYETHYLENE YARN OF HIGH TENACITY HAVING HIGH DIMENSIONAL STABILITY AND METHOD FOR MANUFACTURING THE SAME
20220364273 · 2022-11-17 ·

The present disclosure relates to a polyethylene yarn and a method for manufacturing the same. In the present disclosure, there are provided a polyethylene yarn having excellent dimensional stability and high tenacity, and a method for manufacturing the above polyethylene yarn more efficiently.

Breathable sheet, laminate, and composite

The breathable sheet of the present invention is comprised of a 4-methyl-1-pentene-based polymer or a resin composition containing the 4-methyl-1-pentene-based polymer as a main component. In addition, the breathable sheet of the present invention is preferably selected from the group consisting of a net, a mesh, a non-woven fabric, a woven fabric, and a perforated sheet.

POLYETHYLENE YARN, METHOD FOR MANUFACTURING THE SAME, AND SKIN COOLING FABRIC COMPRISING THE SAME

Disclosed is a polyethylene yarn which enables the manufacture of a skin cooling fabric having dimensional stability and having improved weavability which enables the manufacture of a skin cooling fabric capable of providing a user with a soft tactile sensation as well as a cooling sensation, a method for manufacturing the same, and a skin cooling fabric including the same. The polyethylene yarn has a shrinkage stress at 70° C. and 100° C. of 0.005 to 0.075 g/d, respectively. Also, the polyethylene yarn has a “dry thermal shrinkage rate at 70° C.” of 0.1 to 0.5%, a “dry thermal shrinkage rate at 100° C.” of 0.5 to 1.5%, and a “wet thermal shrinkage rate at 100° C.” of 0.1 to 1%.