Described embodiments include a graphene membrane film for solvent purification and related method, and a solvent purification system using same. The graphene membrane film for solvent purification is formed having a plurality of stacked graphene plate-shaped flakes, and at least one pair of the plurality of stacked graphene plate-shaped flakes comprises a physical bond or a chemical bond connecting layers. The graphene membrane film for solvent purification is produced by preparing a graphene oxide dispersion liquid by dispersing graphene oxide in distilled water; confining the graphene oxide dispersion liquid between a pair of substrates; and applying heat and pressure to the graphene oxide dispersion liquid between the substrates to perform a hydrothermal reaction to concurrently thermally reduce the graphene oxide and bind graphenes. Due to lipophilic surface property and fine pores, size exclusion separation and hydrophilic-lipophilic component separation through polarity may be realized, and thus is usable in fine chemistry fields.

A composite molecular sieve membrane, preparation method and use thereof are provided in the embodiments. The composite molecular sieve membrane includes a support layer and a molecular sieve membrane layer, wherein the support layer is a high-porosity and porous ceramic which is made of nano- or submicron ceramic powder materials or ceramic material precursors prepared through an electrospinning process. The high-porosity and porous ceramic, is adjustable from 40% to 83%. The composite molecular sieve membrane of the embodiments uses the porous ceramic prepared through an electrospinning process as the support layer, and the support layer has a flat and continuous surface, high porosity, uniform and adjustable pore sizes, low-tortuosity pore channels, and high mechanical strength; the flux of the composite molecular sieve membrane is increased, besides, the seed crystals can attach effectively due to the fibrous pore channels of the support layer, ensuring the adhesion amount of seed crystals.

The invention relates to carbon supported crack- and tear-free graphene membranes of large area useful for selective gas separation, method of preparation and uses thereof. In particular, the invention relates to carbon supported crack- and tear-free graphene membranes having good gas separation performance, in particular high H.sub.2 permeance and H.sub.2/CH.sub.4 selectivities.

The invention, belonging to the field of membrane technology, presents a method for the direct growth of ultrathin porous graphene separation membranes. Etching agent, organic solvent and polymer are coated on metal foil, and then they are calcined at high temperature in absence of oxygen; after removal of metal substrate and reaction products, single-layered or multi-layered porous graphene membranes are obtained. Alternatively, the dispersion or solution of etching agent is coated on metal foil, on which a polymer film is then overlaid. The obtained sample is subsequently calcined at high temperature in absence of oxygen; after removal of metal substrate and reaction products, single-layered or multi-layered porous graphene membranes are obtained. The method involved in this invention is simple and highly efficient, and allows direct growth of ultrathin porous graphene separation membranes, without needing expensive apparatuses, chemicals and graphene raw material. Additionally, the graphene membranes prepared with this method have controlled pore size, ultrahigh water flux and strong resistance to irreversible fouling.

The invention relates to a method for preparing a hierarchical porous zeolite membrane and an application thereof, comprising the following steps: a mesoporous structure-directing agent is added to limit the growth of zeolite crystals, and self-assembled in the crystallization process to generate a mesoporous structure. Based on a seed crystal induced secondary nucleation mechanism, this method can realize one-step hydrothermal synthesis of hierarchical porous zeolite membrane with the advantages of mild and controllable synthesis conditions, simple process, good repeatability, reduced energy consumption and cost savings. The hierarchical porous zeolite membrane prepared by the method has good cut-off performance, and the cut-off molecular weight is adjustable between 200 to 500,000 Da.

A method of making a hollow fiber carbon molecular sieve is comprised of heating a hollow polymer fiber to a carbonization temperature in an atmosphere that is non-oxidizing to form a hollow fiber carbon molecular sieve, wherein during at least a portion of the heating a tensile force is applied to the hollow polymer fiber. The method may improve the separation of gases similar in size such a propylene from propane.

A carbon molecular sieve (CMS) membrane having improved separation characteristics for separating olefins from their corresponding paraffins is comprised of carbon with at most trace amounts of sulfur and a group 13 metal. The CMS membrane may be made by pyrolyzing a precursor polymer devoid of sulfur in which the precursor polymer has had a group 13 metal incorporated into it, wherein the metal is in a reduced state. The pyrolyzing for the precursor having the group 13 metal incorporated into it is performed in a nonoxidizing atmosphere and at a heating rate and temperature such that the metal in a reduced state (e.g., covalently bonded to carbon or nitrogen or in the metal state).

A process for preparing a microcapillary carbon molecular sieve membrane may include extruding a polyvinylidene chloride polymer to a thickness from 10 μm to 1,000 μm to form an extruded polymeric microcapillary film, wherein the extruded polymeric microcapillary film comprises a first end, a second end, and one or more microcapillaries extending from the first end to the second end; pre-treating the extruded polymeric microcapillary film at a temperature from 100° C. to 200° C. for a time from 1 hour to 48 hours to form a pre-treated polymeric microcapillary film; and pyrolizing the pre-treated polymeric microcapillary film at a temperature from 200° C. to 1,500° C. for a time from 15 minutes to 5 hours to form the microcapillary carbon molecular sieve membrane.

It is provided a water-saturated carbon molecular sieve membrane obtainable by a) providing a hydrophilic carbon molecular sieve membrane (CMSM) comprising pores of a pore size from 0.25 nm to 0.55 nm for molecular sieving, pores of a pore size from 0.55 nm to 0.90 nm for adsorption diffusion and a negligible amount of pores larger than 0.90 nm such that a plot of N.sub.2 permeance versus pressure of permeation at room temperature and at a pressure from 1 to 4 bar has zero or negative slope; and b) humidifying the membrane until obtaining a water-saturated carbon molecular sieve membrane. It is also provided a process for the separation of a gas from a gas mixture with such a water-saturated membrane, and its use for solvent dehydration, and as a membrane reactor.

A carbon molecular sieve (CMS) membrane having improved separation characteristics for separating olefins from their corresponding paraffins is comprised of carbon with at most trace amounts of sulfur and a group 13 metal. The CMS membrane may be made by pyrolyzing a precursor polymer devoid of sulfur in which the precursor polymer has had a group 13 metal incorporated into it, wherein the metal is in a reduced state. The pyrolyzing for the precursor having the group 13 metal incorporated into it is performed in a nonoxidizing atmosphere and at a heating rate and temperature such that the metal in a reduced state (e.g., covalently bonded to carbon or nitrogen or in the metal state).