Disclosed herein are vapour-phase crosslin ked composite membranes in the form of crosslinked polymers and defined inorganic materials. The membranes disclosed herein may have a narrow pore size distribution and precise molecule separation ability and may be used for organic solvent nanofiltration and organic solvent reverse osmosis. Also disclosed herein are methods of forming the membranes, and filtration. In a preferred embodiment, the vapour-phase crosslinked composite membrane is obtained by exposing a composite membrane comprising polyimide and UiO-66-NH.sub.2 particles to an amine vapour.

Provided herein are methods and systems for production (e.g., batch production) of a polypeptide product via cell culture. In some embodiments, the methods and systems use a first bioreactor (e.g., for cell culturing), an alternating tangential flow (ATF) microfilter (e.g., for removing a polypeptide product and culture medium from the cell culture while retaining cells), a second bioreactor (e.g., for concentrating the product), and an ATF ultrafilter (e.g., for retaining product in the second bioreactor and allowing culture medium to exit).

A method for producing a microporous material comprising the steps of: providing an ultrahigh molecular weight polyethylene (UHMWPE); providing a filler; providing a processing plasticizer; adding the filler to the UHMWPE in a mixture being in the range of from about 1:9 to about 15:1 filler to UHMWPE by weight; adding the processing plasticizer to the mixture; extruding the mixture to form a sheet from the mixture; calendering the sheet; extracting the processing plasticizer from the sheet to produce a matrix comprising UHMWPE and the filler distributed throughout the matrix; stretching the microporous material in at least one direction to a stretch ratio of at least about 1.5 to produce a stretched microporous matrix; and subsequently calendering the stretched microporous matrix to produce a microporous material which exhibits improved physical and dimensional stability properties over the stretched microporous matrix.

Disclosed are compositions that may be useful for forming synthetic membranes, methods of forming membranes therefrom, and membranes. In an embodiment, a membrane comprises a free hydrophilic polymer and a polyurethane, the polyurethane comprising a backbone comprising the reaction product of a diisocyanate, a polymeric aliphatic diol, and, optionally, a chain extender, wherein the backbone comprises a C.sub.2-C.sub.16 fluoroalkyl or C.sub.2-C.sub.16 fluoroalkyl ether, or the polyurethane comprises an endgroup comprising a C.sub.2-C.sub.16 fluoroalkyl or C.sub.2-C.sub.16 fluoroalkyl ether.

This disclosure relates to blended polymeric membranes containing a polyimide polymeric matrix blended with a crosslinked polymer of intrinsic microporosity and methods of using the membranes for gas separation applications, such as removal of CO.sub.2 from natural gas.

The present invention relates to a membrane (M) comprising an amorphous polymer (P) comprising repeat units of the formulas (RU1), (RU2) and (RU3). Moreover, the present invention relates to a process for the preparation of said membrane (M) and a filtration process, wherein a liquid permeates said membrane (M).

An object of the present invention is to provide a polyamide porous membrane having improved fluid permeation performance. A polyamide porous membrane having a dense layer formed on at least one surface, wherein the polyamide porous membrane has a streak-like recessed portion extending in one direction of a surface of the dense layer, and the streak-like recessed portion has an orientation angle of 0 to 5.0° or 175.0 to 180.0° and an orientation intensity of 1.5 to 2.0 according to predetermined orientation analysis.

Provided herein are optimized methods for concentrating large volumes of antibody feedstocks to generate concentrated drug substances by ultrafiltration in a batch-like mode using a fed-batch setup.

The present disclosure relates to the field of materials for uranium extraction from seawater (UES), and in particular, to a photothermal photocatalytic membrane for seawater desalination and uranium extraction and a preparation method therefor. The present disclosure provides a photothermal photocatalytic membrane for seawater desalination and uranium extraction and a preparation method therefor. The preparation method includes: fixing a treated carbon cloth to a glass plate, pouring a casting solution 1 onto the carbon cloth to form a first layer of film, forming a second layer of film using a casting solution 2, and putting the second layer of film into a first coagulation bath and a second coagulation bath in sequence to form the photothermal photocatalytic membrane. The photothermal photocatalytic membrane is supported by the carbon cloth, and a surface of the photothermal photocatalytic membrane is of a micro-nano structure.

In at least one embodiment, a microporous membrane having a moderate to high water vapor permeability and high liquid water penetration resistance is disclosed. The microporous membrane may be used in building applications, including as or as part of a building wrap, a rain screen, a roofing underlayment, a flashing, a sound proofing material, or an insulation material. The microporous membrane may include at least one thermoplastic polymer, at least one filler, and at least one processing oil. The microporous membrane may be flat or may have ribs. The microporous membrane may include at least one scrim component. A method for forming the microporous membrane is also disclosed.