The present invention relates to a lipophilic and hydrophobic nanofiber membrane and a method of preparing the same. The lipophilic and hydrophobic nanofiber membrane according to an exemplary embodiment may be compressed at a pressure of 10 kPa to 100 kPa and may have an average thickness of 10 μm to 1,500 μm.

Provided is a method for manufacturing a long-life brewed alcoholic beverage by a filtration process with the use of a porous membrane involving a washing step, whereby a high tolerance (chemical tolerance) to a washing solution (a chemical solution) and a good filtration performance are achieved. A method for ma manufacturing a second brewed alcoholic beverage which includes: a filtration step for passing a first brewed alcoholic beverage, which contains a yeast and a high-molecular substance or sediment component produced through fermentation by the yeast, through a porous membrane, which is formed of a resin having a three-dimensional network structure, to thereby separate the second brewed alcoholic beverage from the yeast; and a washing step for passing a washing solution through the porous membrane or immersing the porous membrane in the washing solution to thereby wash the inside of the porous membrane.

Provided is a method for manufacturing a long-life brewed alcoholic beverage by a filtration process with the use of a porous membrane involving a washing step, whereby a high tolerance (chemical tolerance) to a washing solution (a chemical solution) and a good filtration performance are achieved. A method for ma manufacturing a second brewed alcoholic beverage which includes: a filtration step for passing a first brewed alcoholic beverage, which contains a yeast and a high-molecular substance or sediment component produced through fermentation by the yeast, through a porous membrane, which is formed of a resin having a three-dimensional network structure, to thereby separate the second brewed alcoholic beverage from the yeast; and a washing step for passing a washing solution through the porous membrane or immersing the porous membrane in the washing solution to thereby wash the inside of the porous membrane.

A water filtration membrane is provided, capable of removing heavy metal ions, filtering out particulates, filtering out bacteria, as well as removing herbicides and volatile organic compounds (VOCs) from water. The membrane is composed of a mat of randomly oriented nanoparticle-coated nanofibers. The nanofibers are covalently bonded to a plurality of substantially uniformly-distributed ceramic nanoparticles embedded in or adhered on the surface of the polymer nanofibers through reactive functional groups. The ceramic nanoparticles have a pattern of deep grooves formed on the nanoparticle surfaces. The bonding of the nanoparticles to the nanofibers is sufficient to retain the nanoparticles on the nanofiber surfaces when water flows through the water filtration membrane. The diameter of the nanofibers is 50-200 nm. The size of the nanoparticles is <40 nm, with a zeta potential of −40 to −45 mV in a dispersion medium. The nanoparticle deep grooves have an average size of approximately 1.2 nm or less.

A water filtration membrane is provided, capable of removing heavy metal ions, filtering out particulates, filtering out bacteria, as well as removing herbicides and volatile organic compounds (VOCs) from water. The membrane is composed of a mat of randomly oriented nanoparticle-coated nanofibers. The nanofibers are covalently bonded to a plurality of substantially uniformly-distributed ceramic nanoparticles embedded in or adhered on the surface of the polymer nanofibers through reactive functional groups. The ceramic nanoparticles have a pattern of deep grooves formed on the nanoparticle surfaces. The bonding of the nanoparticles to the nanofibers is sufficient to retain the nanoparticles on the nanofiber surfaces when water flows through the water filtration membrane. The diameter of the nanofibers is 50-200 nm. The size of the nanoparticles is <40 nm, with a zeta potential of −40 to −45 mV in a dispersion medium. The nanoparticle deep grooves have an average size of approximately 1.2 nm or less.

Polymer-based membranes and methods for fabricating membranes are described. The methods include forming a casting solution featuring a polyvinylidene fluoride (PVDF)-based solvent and a polyvinylpyrrolidone (PVP)-based modifying agent, dispersing the casting solution to form a first element, generating a plurality of active sites on a surface of the first element, and forming a polymer-based membrane by exposing the surface of the first element to a fluorosilane composition to form a fluorosilane layer on the surface, where the fluorosilane composition includes a silane compound having at least one alkyl substituent that includes between 9 and 21 fluorine atoms.

Polymer-based membranes and methods for fabricating membranes are described. The methods include forming a casting solution featuring a polyvinylidene fluoride (PVDF)-based solvent and a polyvinylpyrrolidone (PVP)-based modifying agent, dispersing the casting solution to form a first element, generating a plurality of active sites on a surface of the first element, and forming a polymer-based membrane by exposing the surface of the first element to a fluorosilane composition to form a fluorosilane layer on the surface, where the fluorosilane composition includes a silane compound having at least one alkyl substituent that includes between 9 and 21 fluorine atoms.

A method for preparing a durably hydrophilic and uniform-pore ultrafiltration membrane is disclosed herein. Chemical reactions between the functional groups and the active bonds of the molecular chains in the membrane materials are initiated perform the grafting of hydrophilic chains on the polymer chains under conventional dissolution conditions of the polymer membrane material (dissolution with synchronized hydrophilization), so as to realize durable hydrophilization of the membrane materials. The resulting hydrophilized polymer solution (a nascent-state membrane) is introduced into a coagulation bath to initiate a crosslinking reaction among the hydrophilic chains. The resulting crosslinking serves to synergistically regulate subsequent phase separation and membrane formation (phase separation under synergistic crosslinking).

A method for preparing a durably hydrophilic and uniform-pore ultrafiltration membrane is disclosed herein. Chemical reactions between the functional groups and the active bonds of the molecular chains in the membrane materials are initiated perform the grafting of hydrophilic chains on the polymer chains under conventional dissolution conditions of the polymer membrane material (dissolution with synchronized hydrophilization), so as to realize durable hydrophilization of the membrane materials. The resulting hydrophilized polymer solution (a nascent-state membrane) is introduced into a coagulation bath to initiate a crosslinking reaction among the hydrophilic chains. The resulting crosslinking serves to synergistically regulate subsequent phase separation and membrane formation (phase separation under synergistic crosslinking).

The disclosure is directed to a device that includes an upper container configured to receive a fluid sample collected from a mammal into a first opening, the first opening opposite a second opening and a membrane covering at least a portion of the second opening, the membrane configured to allow transmission of a portion of the fluid sample through the membrane.