A semi-porous composite membrane and a method of manufacturing the semi-porous composite membrane. The semi-porous composite membrane includes a base supporting substrate comprising α-Al.sub.2O.sub.3, an outer layer comprising silica, and an intermediate layer comprising crystalline fibers of boehmite, and at least one of a secondary metal oxide and a synthetic polymer, wherein the intermediate layer is disposed between the base supporting substrate and the outer layer. The crystalline fibers of boehmite are a length of 5-150 nm. The semi-porous composite membrane may be employed in membrane reactors.

A method for removing silica from ultra pure water (UPW) comprises passing UPW through a filter comprising a microporous cationically charged membrane having an upstream surface and a downstream surface; and a porous asymmetric membrane having a first surface and an upstream portion and a downstream portion and a second surface, and a bulk between the first surface and the second surface including the upstream portion and the downstream portion, the porous asymmetric membrane having decreasing pore sizes in a direction from the first surface and the upstream portion to the downstream portion and the second surface, the second surface comprising a skin having a nanoporous average pore size, wherein the first surface of the porous asymmetric membrane contacts the downstream surface of the microporous cationically charged membrane; the method including passing the UPW through the microporous cationically charged membrane before passing the UPW through the porous asymmetric membrane.

The present invention is concerned with the treatment of produced water, obtained from a chemically enhanced oil recovery process using viscosity-increasing polymeric compounds. Said treatment comprises particularly the steps of obtaining a produced water, from an oil-water mixture recovered from an oil-bearing formation, wherein the produced water comprises the viscosity-increasing polymeric compounds; and, of directing the produced water to a specific filtration device, and subjecting the produced water to filtration, for obtaining a retentate stream and a permeate stream. Said process allows particularly obtaining a permeate comprising the viscosity-increasing polymeric compounds, said permeate being substantially free of suspended solids, free oil and emulsified oil.

Membranes, methods of making the membranes, and methods of using the membranes are described herein. The membrane can comprise a support layer; and a selective polymer layer disposed (e.g., coated) on the support layer. The selective polymer layer can comprise a polymer matrix (e.g., a hydrophilic polymer, an amine-containing polymer, or a combination thereof), and a guanidine-based mobile carrier dispersed within the polymer matrix. Optionally, the selective polymer later can further include an amine-based mobile carrier, a CO.sub.2-philic ether, a graphene oxide, carbon nanotubes, or a combination thereof, dispersed within the polymer matrix. The membranes can be used to separate carbon dioxide from other gases, such as hydrogen and/or nitrogen. Also provided are methods of separating gas streams using the membranes described herein.

Provided herein are CO.sub.2-selective membranes that can be used to efficiently separate CO.sub.2 and CO. The membranes can be used to produce high-purity CO.sub.2 and CO gas streams from a feed gas stream comprising a mixture of CO.sub.2 and CO (e.g., an exhaust gas stream from a fuel cell, such as a solid oxide fuel cell). In this way, the membranes can be used with a solid oxide fuel cell system to covert CO.sub.2 to CO.

Highly energy efficient electrodialysis membranes having low operating costs and a novel process for their manufacture are described herein. The membranes are useful in the desalination of water and purification of waste water. They are effective in desalination of seawater due to their low electrical resistance and high permselectivity. These membranes are made by a novel process which results in membranes significantly thinner than prior art commercial electrodialysis membranes. The membranes are produced by polymerizing one or more monofunctional ionogenic monomers with at least one multifunctional monomer in the pores of a porous substrate.

A method of fabricating a gas separation membrane includes providing a coextruded multilayer film that includes a first polymer layer formed of a first polymer material and a second polymer layer formed of a second polymer material, the first polymer material having a first gas permeability. The coextruded multilayer film is axially oriented such that the second polymer layer has a second gas permeability that is greater than the first gas permeability.

A membrane for fluid species transport includes a porous substrate and a selective-transport layer comprising 2-D-material flakes. The porous substrate defines surface pores with dimensions larger than 2 microns, and the selective-transport layer coats the porous substrate and spans across the surface pores. The porous substrate can be contacted with a liquid or coating to fill or coat the surface pores of the porous substrate. Next, a 2-D-material-flake solution is deposited on the porous substrate. Evaporation of solvent from the deposited 2-D-material-flake solution forms the selective-transport layer.

Embodiments of the present disclosure provide for polystyrene-b-polyethylene oxide (PS-b-PEO) block copolymer nanoporous membranes, methods of making a PS-b-PEO block copolymer nanoporous membrane, methods of using PS-b-PEO block copolymer nanoporous membranes, and the like.

A method suppresses membrane thickness variation and air resistance variation after a compression at 60° C. or 80° C. Stretching is performed at least twice in at least different axial directions before the extraction of the solvent, and at the same time, at least one of (i) and (ii) is satisfied. (i) The step (c) is a first stretching step of stretching the sheet-shaped product at least once in a sheet transport direction (MD direction) and at least once in a sheet width direction (TD direction) individually, and the MD stretching magnification and the TD stretching magnification in the step (c) satisfy (TD stretching magnification≥MD stretching magnification−2). (ii) The stretching temperature (T1) of a first axial stretching performed firstly in the step (c) and the maximal stretching temperature (T2) of a second stretching performed after the first axial stretching satisfy (T1−T2≥0).