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 are provide a cell separation filter with which cells can be separated without damage and can suppress adsorption, a filtering device, and a manufacturing method for a cell separation filter. The cell separation filter is composed of a nonwoven fabric that is formed of fibers containing a water-insoluble polymer and a hydrophilizing agent and has a fiber density difference in the film thickness direction. The nonwoven fabric has an average through-hole diameter of 2.0 μm or more and less than 10.0 μm, a void ratio of 75% or more and 98% or less, a film thickness of 100 μm or more, and a critical wet surface tension of 72 mN/m or more.

The invention provides a dynamic membrane reactor with function of nitrogen and phosphorus removal and an operation method thereof, and comprises a biological treatment system, a dynamic membrane loading system and an automatic system. The operation method comprises the following steps. (1) Before the formation of dynamic membrane, a porous filter for phosphorus removal is used as a cathode, a conductive precision filter screen is used as an anode, and aerobic denitrifying bacteria are inoculated into the dynamic membrane reactor under certain constant current density, hydraulic retention time and flux. (2) After the dynamic membrane is formed, the porous filter for phosphorus removal is used as the anode, the conductive precision filter screen is used as the cathode. And intermittent aeration is started at the anode under certain constant current density. (3) When the transmembrane pressure difference exceeds a certain range, hydraulic backwashing is performed under certain constant current density.

The invention provides a dynamic membrane reactor with function of nitrogen and phosphorus removal and an operation method thereof, and comprises a biological treatment system, a dynamic membrane loading system and an automatic system. The operation method comprises the following steps. (1) Before the formation of dynamic membrane, a porous filter for phosphorus removal is used as a cathode, a conductive precision filter screen is used as an anode, and aerobic denitrifying bacteria are inoculated into the dynamic membrane reactor under certain constant current density, hydraulic retention time and flux. (2) After the dynamic membrane is formed, the porous filter for phosphorus removal is used as the anode, the conductive precision filter screen is used as the cathode. And intermittent aeration is started at the anode under certain constant current density. (3) When the transmembrane pressure difference exceeds a certain range, hydraulic backwashing is performed under certain constant current density.

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.

An asymmetric polyvinylidene chloride copolymer membrane is made by a method using a dope solution comprised of a polyvinylidene chloride copolymer and a solvent that solubilizes the polyvinylidene chloride copolymer that is shaped to form an initial shaped membrane. The initial shaped membrane is then quenched in a liquid comprised of a solvent that is miscible with the solvent that solubilizes the polyvinylidene chloride copolymer but is immiscible with the polyvinylidene chloride copolymer to form a wet asymmetric polyvinylidene chloride copolymer membrane. The solvents are removed from the wet membrane to form the asymmetric polyvinylidene chloride (PVDC) copolymer membrane. The membrane then may be further heated to form a carbon asymmetric membrane in which the porous support structure and separation layer of the PVDC membrane is maintained. The asymmetric carbon membrane may be useful to separate gases such as olefins from their corresponding paraffins, hydrogen from syngas or cracked gas, natural gas or refinery gas, oxygen/nitrogen, or carbon dioxide and methane.

An asymmetric polyvinylidene chloride copolymer membrane is made by a method using a dope solution comprised of a polyvinylidene chloride copolymer and a solvent that solubilizes the polyvinylidene chloride copolymer that is shaped to form an initial shaped membrane. The initial shaped membrane is then quenched in a liquid comprised of a solvent that is miscible with the solvent that solubilizes the polyvinylidene chloride copolymer but is immiscible with the polyvinylidene chloride copolymer to form a wet asymmetric polyvinylidene chloride copolymer membrane. The solvents are removed from the wet membrane to form the asymmetric polyvinylidene chloride (PVDC) copolymer membrane. The membrane then may be further heated to form a carbon asymmetric membrane in which the porous support structure and separation layer of the PVDC membrane is maintained. The asymmetric carbon membrane may be useful to separate gases such as olefins from their corresponding paraffins, hydrogen from syngas or cracked gas, natural gas or refinery gas, oxygen/nitrogen, or carbon dioxide and methane.

An ion-sensitive substance containing a crown ether structure composed of a repeating unit represented by formula (a): —CR.sup.1R.sup.2—CR.sup.3X—O— . . . (a) (in the formula, X is an organic group having an alkoxysilyl group at a terminal, and R.sup.1, R.sup.2 and R.sup.3 are each a hydrogen atom or a hydrocarbon group), and a part or all of the alkoxysilyl groups in the crown ether structure may be hydrolyzed to form a silanol group.

An ion-sensitive substance containing a crown ether structure composed of a repeating unit represented by formula (a): —CR.sup.1R.sup.2—CR.sup.3X—O— . . . (a) (in the formula, X is an organic group having an alkoxysilyl group at a terminal, and R.sup.1, R.sup.2 and R.sup.3 are each a hydrogen atom or a hydrocarbon group), and a part or all of the alkoxysilyl groups in the crown ether structure may be hydrolyzed to form a silanol group.

A porous membrane includes a modacrylic copolymer. The modacrylic copolymer includes, with respect to 100 parts by mass of all structural units constituting the modacrylic copolymer, 15 to 85 parts by mass of a structural unit derived from acrylonitrile, 15 to 85 parts by mass of a structural unit derived from at least one halogen-containing monomer selected from the group consisting of vinyl halide and vinylidene halide, and 0 to 10 parts by mass of a structural unit derived from a vinyl monomer having an ionic substituent. The porous membrane can be produced by preparing a modacrylic copolymer solution by dissolving the modacrylic copolymer in a solvent, and bringing the modacrylic copolymer solution into contact with a non-solvent for the modacrylic copolymer such that the modacrylic copolymer solution is solidified.