A method of manufacturing an elastic polymer aerogel material includes dissolving tire waste in a first portion of a solvent to form a first mixture; dissolving a polymer having at least one double carbon-carbon bond in a second portion of the solvent to form a second mixture; combining the first mixture and the second mixture, wherein the tire waste reacts with the polymer having at least one double carbon-carbon bond to form a reactant gel; and undergoing a solvent exchange on the reactant gel followed by freeze drying the reactant gel to form the elastic polymer aerogel material. The tire waste includes natural rubber, synthetic polymers, steel, and curing systems, and the elastic polymer aerogel material defines a 3D porous structure.

An antimicrobial photoactive nanofibrous polymer material with polymer nanofibers has hydrophobic domains and hydrophilic domains. At least one photoactive molecule encapsulated in the hydrophobic domains of the polymer nanofibers is a photoactive molecule being capable of releasing or generating an antimicrobially active substance after irradiation by visible light. The antimicrobial photoactive nanofibrous polymer material may be used for antimicrobial wound dressings, antimicrobial cosmetic facial masks, self-disinfecting face masks or respirators, self-disinfecting filters for filtration of gases or liquids, self-disinfecting textile and products made thereof, self-disinfecting packaging material or protective agriculture foils.

An antimicrobial photoactive nanofibrous polymer material with polymer nanofibers has hydrophobic domains and hydrophilic domains. At least one photoactive molecule encapsulated in the hydrophobic domains of the polymer nanofibers is a photoactive molecule being capable of releasing or generating an antimicrobially active substance after irradiation by visible light. The antimicrobial photoactive nanofibrous polymer material may be used for antimicrobial wound dressings, antimicrobial cosmetic facial masks, self-disinfecting face masks or respirators, self-disinfecting filters for filtration of gases or liquids, self-disinfecting textile and products made thereof, self-disinfecting packaging material or protective agriculture foils.

Porous and microporous parts prepared by additive manufacturing as disclosed herein are useful in medical and non-medical applications. The parts are prepared from a composition containing both a solvent soluble component and a solvent insoluble component. After a part is printed by an additive manufacturing process it is exposed to solvent to extract solvent soluble component away front the printed part, resulting in a part having surface cavities.

The present invention relates generally to compositions for use in biological and chemical separations, as well as other applications. More specifically, the present invention relates to hybrid felts fabricated from electrospun nanofibers with high permeance and high capacity. Such hybrid felts utilize derivatized cellulose, and at least one non-cellulose-based polymer that may be removed from the felt by subjecting it to moderately elevated temperatures and/or solvents capable of dissolving the non-cellulose-based polymer to leave behind a porous nanofiber felt having more uniform pore sizes and other enhanced properties when compared to single component nanofiber felts.

The present invention relates generally to compositions for use in biological and chemical separations, as well as other applications. More specifically, the present invention relates to hybrid felts fabricated from electrospun nanofibers with high permeance and high capacity. Such hybrid felts utilize derivatized cellulose, and at least one non-cellulose-based polymer that may be removed from the felt by subjecting it to moderately elevated temperatures and/or solvents capable of dissolving the non-cellulose-based polymer to leave behind a porous nanofiber felt having more uniform pore sizes and other enhanced properties when compared to single component nanofiber felts.

Porous and microporous parts prepared by additive manufacturing as disclosed herein are useful in medical and non-medical applications. The parts are prepared from a composition containing both a solvent soluble component and a solvent insoluble component. After a part is printed by an additive manufacturing process it is exposed to solvent to extract solvent soluble component away from the printed part, resulting in a part having surface cavities.

A cooling material is provided. The cooling material can include a yarn having a defined denier of less than or equal to approximately 90 denier, wherein the yarn can comprise a cooling additive disposed on or in a polymer. In some embodiments, the yarn can be at least one of a warp or a weft of a woven fabric. A method can comprise receiving a cooling material, wherein the cooling material comprises: a polymer and a cooling additive, wherein the cooling additive is disposed on or in the polymer; and processing the cooling material by employing a non-weaving technique to create a non-woven fabric. In some embodiments, the non-weaving technique is one of a meltblown process, a spunbond process, or a multi-denier process.

A cooling material is provided. The cooling material can include a yarn having a defined denier of less than or equal to approximately 90 denier, wherein the yarn can comprise a cooling additive disposed on or in a polymer. In some embodiments, the yarn can be at least one of a warp or a weft of a woven fabric. A method can comprise receiving a cooling material, wherein the cooling material comprises: a polymer and a cooling additive, wherein the cooling additive is disposed on or in the polymer; and processing the cooling material by employing a non-weaving technique to create a non-woven fabric. In some embodiments, the non-weaving technique is one of a meltblown process, a spunbond process, or a multi-denier process.

The present invention relates to electrospun fibers comprising i) a hydrophilic polymer that is soluble in a first solvent, ii) a bioadhesive substance that is slightly soluble in said first solvent, iii) optionally, a drug substance.