The present invention relates to a graphene-based or other 2-D material membrane which allows the passage of protons and deuterons and to a method of facilitating proton or deuteron permeation through such a membrane. Monocrystalline membranes made from mono- and few-layers of graphene, hBN, molybdenum disulfide (MoS2), and tungsten disulfide (WS2) etc. are disclosed. In effect, the protons or deuterons are charge carriers that pass through the graphene or other 2-D material membrane. This process can be contrasted with the passage of gaseous hydrogen. Hydrogen is an uncharged gaseous species which is diatomic. In other words, the gas is in molecular form when considering the normal barrier properties whereas in the case of the present invention, the species which is being transported through the membrane is a charged ion comprising a single atom. Membranes of the invention find use in a number of applications such as fuel cells.

Described herein is a crosslinked graphene and biopolymer (e.g. lignin) based composite membrane that provides selective resistance for gases while providing water vapor permeability. Methods for making such membranes, and methods of using the membranes for dehydrating mixtures, are also described.

The present disclosure relates to methods for producing large scale nanostructured material comprising carbon nanotubes. Therefore, there is disclosed a method for making nanostructured materials comprising depositing carbon nanotubes onto at least one substrate via a deposition station, wherein depositing comprises transporting molecules to the substrate from a deposition fluid, such as liquid or gas. By using a substrate that is permeable to the carrier fluid, and allowing the carrier fluid to flow through the substrate by differential pressure filtration, a nanostructured material can be formed on the substrate, which may be removed, or may act as a part of the final component.

Provided is a filter unit including conductive filters having permeation holes, a pair of electrodes configured to apply a voltage to the conductive filters, and an insulator configured to prevent a current from flowing between the pair of electrodes.

Fluid reactors include a sealed housing enclosing a reactor core that includes at least one substrate-free multichannel reactor core element. Each reactor core element is made from a non-substrate mounted, open pore cellular network material having an asymmetric, tortuous, bi-continuous two-phase material structure and contains multiple perforating fluid channels. Multiple reactor core elements can be serially and/or parallelly piped in a sealed manner to form a reactor core for a fluid reactor with a higher production capacity.

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 on the support layer. The selective polymer layer can comprise a selective polymer matrix (e.g., hydrophilic polymer, an amine-containing polymer, a low molecular weight amino compound, a CO.sub.2-philic ether, or a combination thereof), and graphene oxide dispersed within the selective polymer matrix. The membranes can be used to separate carbon dioxide for hydrogen. Also provided are methods of purifying syngas using the membranes described herein.

A supported carbon molecular sieve (CMS) membrane is made by contacting a film of a carbon forming polymer on a polymer textile to form a laminate. The laminate is then heated to a temperature for a time under an atmosphere sufficient to carbonize the film and polymer textile to form the supported CMS membrane. The supported CMS membrane formed is a laminate having a carbon separating layer graphitically bonded to a carbon textile, wherein the carbon separating layer is a continuous film. The supported CMS membranes are particularly useful for separating gases such as olefins from their corresponding paraffins.

There is provided a system and method for angstrom confinement of trapped ions. The method including: receiving water molecules and ionic compounds in a first reservoir, an angstrom confinement assembly is positioned between the first reservoir and a second reservoir, the angstrom confinement assembly defining angstrom conduits; and repeatedly applying an electric field across a first electrode and a second electrode, the first electrode on a same side of the angstrom confinement assembly as the first reservoir and the second electrode on a same side of the angstrom confinement assembly as the second reservoir, the electric field applied such that, when the electric field is applied, positive ions of the ionic compounds are induced to flow through the angstrom conduits, and wherein, when the electric field is not applied, water molecules flow into the angstrom conduits due to capillary forces to confine the positive ions in the angstrom conduits.

The present invention provides an asymmetric modified CMS hollow fiber membrane having improved gas separation performance properties and a process for preparing an asymmetric modified CMS hollow fiber membrane having improved gas separation performance properties. The process comprises treating a polymeric precursor fiber with a solution containing a modifying agent prior to pyrolysis. The concentration of the modifying agent in the solution may be selected in order to obtain an asymmetric modified CMS hollow fiber membrane having a desired combination of gas permeance and selectivity properties. The treated precursor fiber is then pyrolyzed to form an asymmetric modified CMS hollow fiber membrane having improved gas permeance.

Composite materials for removing hydrophobic components from a fluid include a porous matrix polymer, carbon nanotubes grafted to surfaces of the porous matrix polymer, and polystyrene chains grafted to the carbon nanotubes. Examples of porous matrix polymer include polyurethanes, polyethylenes, and polypropylenes. Membranes of the composite material may be enclosed within a fluid-permeable pouch to form a fluid treatment apparatus, such that by contacting the apparatus with a fluid mixture containing water and a hydrophobic component, the hydrophobic component absorbs selectively into the membrane. The apparatus may be removed from the fluid mixture and reused after the hydrophobic component is expelled from the membrane. The composite material may be prepared by grafting functionalized carbon nanotubes to a porous matrix polymer to form a polymer-nanotube composite, then polymerizing styrene onto the carbon nanotubes of the polymer-nanotube composite.