Patent classifications
B01D71/301
Filtration Filter And Method For Producing The Same
A filtration filter for filtering out impurities has a support with a fibrous structure. A filtration membrane is integrally formed inside the support. The filtration membrane includes a porous resin and is capable of filtering out impurities. The filtration membrane includes a porous resin membrane having an average pore size of 0.026 μm and an opening ratio of 6% to 30%.
METHOD FOR PREPARING DURABLY HYDROPHILIC AND UNIFORM-PORE ULTRAFILTRATION MEMBRANE
A method for preparing a durably hydrophilic and uniform-pore ultrafiltration membrane is disclosed herein. Chemical reactions between the functional groups and the active bonds of the molecular chains in the membrane materials are initiated perform the grafting of hydrophilic chains on the polymer chains under conventional dissolution conditions of the polymer membrane material (dissolution with synchronized hydrophilization), so as to realize durable hydrophilization of the membrane materials. The resulting hydrophilized polymer solution (a nascent-state membrane) is introduced into a coagulation bath to initiate a crosslinking reaction among the hydrophilic chains. The resulting crosslinking serves to synergistically regulate subsequent phase separation and membrane formation (phase separation under synergistic crosslinking).
CATION EXCHANGE MEMBRANE AND METHOD FOR PRODUCING SAME
A cation-exchange membrane using a polyolefin-based substrate with reduced swelling of an ion-exchange resin and a low electrical resistance is provided. The cation-exchange membrane of the present invention includes a substrate made of polyolefin-based woven fabric, and a sulfonic acid group-containing cation-exchange resin. A portion of the cation-exchange membrane other than the substrate has 23 mass % or more to 35 mass % or less of polyvinyl chloride.
Supported carbon molecular sieve membranes and method to form them
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.
MAGNESIUM ION SELECTIVE MEMBRANES
Magnesium ion selective electrode membranes and the preparation thereof. The membranes are rendered highly selective for magnesium ions by the addition of acidic groups to the preferably PVC membrane, either by introducing a lipophilic compound comprising an acidic group covalently linked to a C4-C18 alkyl-substituted phenyl group (e.g. bis-4-octylphenyl phosphoric acid) into the membrane comprising the magnesium selective ionophore (e.g. a neutral ionophore 1,10-phenanthroline derivative) or by covalently linking an acidic (e.g. a carboxylic) group to the ionophore (e.g. a 1,10- phenanthroline derivative).
SUPPORTED CARBON MOLECULAR SIEVE MEMBRANES AND METHOD TO FORM THEM
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.
MICROPOROUS MEMBRANES, UNDERLAYMENT, ROOFING, FLASHING, WRAP, AND METHODS FOR MAKING AND USING THE SAME
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.
FLAT SHEET POROUS MEMBRANE
The disclosed technology relates to flat sheet porous membranes prepared from a dope solution containing a polymer of vinyl chloride, such as chlorinated polyvinyl chloride.
Porous membrane and method of production thereof
The invention provides a porous membrane comprising polyvinyl chloride (PVC) and at least one inorganic filler embedded in the porous membrane wherein the inorganic filler comprises sulfuric acid precipitated silica. The invention further provides a process for the production of said porous membrane.
Separation of gases via carbonized vinylidene chloride copolymer gas separation membranes and processes therefor
A process for separating hydrogen from a gas mixture having hydrogen and a larger gas molecule is comprised of flowing the gas mixture through a carbonized polyvinylidene chloride (PVDC) copolymer membrane having a hydrogen permeance in combination with a hydrogen/methane selectivity, wherein the combination of hydrogen permeance and hydrogen/methane selectivity is (i) at least 30 GPU hydrogen permeance and at least 200 hydrogen/methane selectivity or (ii) at least 10 GPU hydrogen permeance and at least 700 hydrogen/methane selectivity. The carbonized PVDC copolymer may be made by heating and restraining a polyvinylidene chloride copolymer film or hollow fiber having a thickness of 1 micrometer to 250 micrometers to a pretreatment temperature of 100? C. to 180? C. to form a pretreated polyvinylidene chloride copolymer film and then heating and restraining the pretreated polyvinylidene chloride copolymer film to a maximum pyrolysis temperature from 350? C. to 750? C.