A composite that includes an expanded polytetrafluoroethylene (ePTFE) membrane having a porous microstructure. The porous microstructure of the ePTFE membrane is impregnated with a stiffening polymer. An acoustic device assembly that includes the composite and an acoustic device is also described. The composite and the acoustic device assembly can exhibit an insertion loss of less than 7 dB at 1 kHz when measured by the Acoustic Response Measurement (“ARM”) Test.

A perfluorocarbon-free membrane composed of a non-perfluorocarbon material having a first side and a second side opposite of the first side. The perfluorocarbon-free membrane also includes a plurality of pores, each having an inlet and outlet and each passing through the non-perfluorocarbon material so that each pore provides fluidic communication between the first and second sides of the non-perfluorocarbon material. A portion of the non-perfluorocarbon material extends over the inlet and outlet of each the plurality of pores so that a cross-sectional area of the inlets and outlets in a direction of the extension of the non-perfluorocarbon material is smaller than a cross-sectional area of the respective pore in the direction of the extension of the non-perfluorocarbon material. The perfluorocarbon-free membrane does not include a hydrophobic perfluorocarbon coating.

A spin dope composition produces a polymeric fiber useful in non-cryogenic gas separation. The composition includes polysulfone as the polymeric component, two solvents, in which the polymer is soluble, and a non-solvent, in which the polymer is insoluble. The solvents preferably include N-methyl-pyrrolidone (NMP) and N,N-dimethyl acetamide (DMAC), and the non-solvent preferably includes triethylene glycol (TEG). Fibers made from the present composition have been found to exhibit superior properties of gas flux and selectivity, as compared with fibers made from spin dopes having only one solvent component.

A hybrid type filtration structure for filtering liquid includes a first active layer, a porous supporting layer and a permeable layer. The first active layer has a first nano pore inner wall of which a function group included compound is combined with. The porous supporting layer has a plurality of pores and is disposed under the first active layer. The permeable layer is disposed under the porous supporting layer. The porous supporting layer includes a plurality of lipid bilayers having membrane protein inside of the pore, a molecule of water selectively passes through the membrane protein. The first nano pore passes through the first active layer vertically. The first nano pore and the pore are connected with each other through which liquid flows.

A catalytic composite is formed of a catalytic layered assembly including a porous catalytic fluoropolymer film and one or more felt batts connected with the porous catalytic fluoropolymer film. At least one felt batt is positioned adjacent the upstream side of the porous catalytic fluoropolymer film to form the catalytic composite. The fluoropolymer film is perforated to allow for enhanced airflow therethrough while retaining the capability of catalyzing the reduction or removal of chemical species in fluid flowing through the catalytic composite.

A polyolefin microporous membrane is disclosed. The membrane has a width of not less than 100 mm, and a variation range of an F25 value in a width direction is not greater than 1 MPa. The F25 value is a value obtained by dividing a load at 25% elongation of a sample of the laminated polyolefin microporous membrane as measured with a tensile testing machine by a cross-sectional area of the sample.

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).

The present invention provides a porous membrane for water treatment, comprising: a high molecular weight polyethylene, a water-soluble polymer and an antioxidant, the high molecular weight polyethylene having an average molecular weight of 1.0×10.sup.5 to 10.0×10.sup.6 and a density of 0.940 to 0.976 g/cm.sup.3; wherein, the weight of the water-soluble polymer is 5 to 50 parts, the weight of the antioxidant is 0.1 to 10 parts, based on 100 parts of the weight of the high molecular weight polyethylene. The porous membrane for water treatment prepared by the present invention has a thickness of 5 to 30 μm, a pore size of 10 to 100 nm, a porosity of 20 to 60%, and a surface contact angle of 30° to 95°. The porous membrane according to the present invention has good durability, simple preparation process, and relatively thin thickness, a uniform pore size distribution and small pore size, good hydrophilicity, as well as good filtration and adsorption effect.

Described herein are systems and methods for liquid phase separation for fuel tanks and other vessels. Particularly, aspects of the present disclosure are directed to a backpressure regulator configured to open when pressure of a mixture upstream of the backpressure regulator exceeds a predetermined setpoint and a hydrophobic membrane upstream of the backpressure regulator and downstream of a first conduit. The predetermined setpoint may be determined by at least a bubble point pressure of the hydrophobic membrane. Additionally, the backpressure regulator may be fluidically connected to and downstream of the first conduit, and to at least one pump operably connected to and upstream of the first conduit and the hydrophobic membrane may be fluidically connected to and upstream of a second conduit. The backpressure regulator may be fluidically connected to and upstream of a third conduit and the third conduit may be downstream the first conduit.

A microporous membrane has average membrane thickness of 15 μm or less, and relative impedance A after a heat compression treatment under a pressure of 4.0 MPa at 80° C. for 10 minutes of 140% or less, the relative impedance A being obtained by the equation below: Relative impedance A=(impedance measured at 80° C. after the heat compression treatment)/(impedance measured at room temperature prior to the heat compression treatment)×100.