A nanocomposite including an array of extended length fibers with nanofibers oriented in transverse relation to the extended length fibers. The nanofibers are mechanically interlocked with the extended length fibers using a connecting agent concentrated at contact locations between the extended length fibers and the nanofibers without saturating the composite. The resultant composite of fibers and connecting agent is characterized by significant internal porosity with an internal void volume not occupied by the connecting agent.

An aerogel that includes an open-cell structured polymer matrix that can have 5 wt. % to 50 wt. % of a polyamic amide polymer, based on the total weight of the aerogel is disclosed. The aerogel can have a density of 0.05 g/cm.sup.3 to 0.35 g/cm.sup.3 and can be thermally stable to resist browning at 330° C.

An aerogel that includes an open-cell structured polymer matrix that can have 5 wt. % to 50 wt. % of a polyamic amide polymer, based on the total weight of the aerogel is disclosed. The aerogel can have a density of 0.05 g/cm.sup.3 to 0.35 g/cm.sup.3 and can be thermally stable to resist browning at 330° C.

The present disclosure belongs to the technical field of hemostatic materials, and specifically relates to a degradable hemostatic sponge and a preparation method and use thereof, and a degradable drug-loaded hemostatic sponge. The degradable hemostatic sponge provided by the present disclosure is prepared from raw materials including a crosslinking-modified starch and a cellulose through freeze-drying, where a mass ratio of the crosslinking-modified starch to the cellulose is (0.2-5):1. The degradable hemostatic sponge provided by the present disclosure has a high water-absorbing rate and a large water-absorbing capacity, shows a high support strength and a long support time after water absorption, and is made from plant-derived raw materials and thus may be completely biodegraded. The degradable drug-loaded starch hemostatic sponge provided by the present disclosure has a drug-loaded coating attached to a surface of the sponge, where the drug is slowly released while a support is maintained.

The present disclosure belongs to the technical field of hemostatic materials, and specifically relates to a degradable hemostatic sponge and a preparation method and use thereof, and a degradable drug-loaded hemostatic sponge. The degradable hemostatic sponge provided by the present disclosure is prepared from raw materials including a crosslinking-modified starch and a cellulose through freeze-drying, where a mass ratio of the crosslinking-modified starch to the cellulose is (0.2-5):1. The degradable hemostatic sponge provided by the present disclosure has a high water-absorbing rate and a large water-absorbing capacity, shows a high support strength and a long support time after water absorption, and is made from plant-derived raw materials and thus may be completely biodegraded. The degradable drug-loaded starch hemostatic sponge provided by the present disclosure has a drug-loaded coating attached to a surface of the sponge, where the drug is slowly released while a support is maintained.

A method for producing a breathable film based on polyvinyl chloride (PVC), including the following steps. Preparing a paste-like compound including a first fraction composed of PVC, a second fraction composed of a foreign material, and a third fraction composed of adjuvants and/or additives that that are mixed together to form the paste-like compound, applying the paste-like compound to a base, and drying and gelling the paste-like compound, which has been applied to the base, through the addition of heat, thus forming the film in which pores extending from the one surface of the film to the other are formed, which give the film breathability.

A method for producing a breathable film based on polyvinyl chloride (PVC), including the following steps. Preparing a paste-like compound including a first fraction composed of PVC, a second fraction composed of a foreign material, and a third fraction composed of adjuvants and/or additives that that are mixed together to form the paste-like compound, applying the paste-like compound to a base, and drying and gelling the paste-like compound, which has been applied to the base, through the addition of heat, thus forming the film in which pores extending from the one surface of the film to the other are formed, which give the film breathability.

A BAK removal device is constructed as a plug of microparticles of a hydrophilic polymeric gel that displays a hydraulic permeability greater than 0.01 Da. The polymer hydrophilic polymeric gel comprises poly(2-hydroxyethyl methacrylate) (pHEMA). The particles are 2 to 100 μm and the plug has a surface area of 30 mm.sup.2 to 2 mm.sup.2 and a length of 2 mm to 25 mm and wherein the microparticles of a hydrophilic polymeric gel has a pore radius of 3 to 60 μm.

Microporous polyolefin and microporous polydicyclopentadiene (polyDCPD) based aerogels and methods for preparing and using the same are provided. The aerogels are produced by forming a polymer gel structure within a solvent from a olefin or dicyclopentadiene monomer via Ring Opening Metathesis Polymerization (ROMP) reactions, followed by supercritical drying to remove the solvent from the aerogel. Other aerogels are prepared by sequentially (1) mixing at least one dicyclopentadiene monomer, at least one solvent at least one catalyst and at least one inorganic and/or organic reinforcing material, (2) gelling the mixture, (3) aging, and (4) supercritical drying. Aerogels provided herein are inexpensive to prepare, possess desirable thermal, mechanical, acoustic, chemical, and physical properties and are hydrophobic. The aerogels provided herein are suitable for use in various applications, including but not limited to thermal and acoustic insulation, radiation shielding, and vibrational damping applications.

Microporous polyolefin and microporous polydicyclopentadiene (polyDCPD) based aerogels and methods for preparing and using the same are provided. The aerogels are produced by forming a polymer gel structure within a solvent from a olefin or dicyclopentadiene monomer via Ring Opening Metathesis Polymerization (ROMP) reactions, followed by supercritical drying to remove the solvent from the aerogel. Other aerogels are prepared by sequentially (1) mixing at least one dicyclopentadiene monomer, at least one solvent at least one catalyst and at least one inorganic and/or organic reinforcing material, (2) gelling the mixture, (3) aging, and (4) supercritical drying. Aerogels provided herein are inexpensive to prepare, possess desirable thermal, mechanical, acoustic, chemical, and physical properties and are hydrophobic. The aerogels provided herein are suitable for use in various applications, including but not limited to thermal and acoustic insulation, radiation shielding, and vibrational damping applications.