When the porous membrane, which has two surfaces of a surface A and a surface C, is equally divided in the thickness direction of the porous membrane into three layers of a first layer including the surface A, a second layer that is a central layer in the thickness direction, and a third layer including the surface C, an average trunk size of the third layer is larger than an average trunk size of the second layer, and when a continuous layer from the surface A having a thickness of 10 m in the first layer is a first layer component, a continuous layer component having a thickness of 10 m and an average trunk size smaller than an average trunk size of the first layer component is present in the first layer, the second layer, and the third layer other than the first layer component.

When the porous membrane, which has two surfaces of a surface A and a surface C, is equally divided in the thickness direction of the porous membrane into three layers of a first layer including the surface A, a second layer that is a central layer in the thickness direction, and a third layer including the surface C, an average trunk size of the third layer is larger than an average trunk size of the second layer, and when a continuous layer from the surface A having a thickness of 10 m in the first layer is a first layer component, a continuous layer component having a thickness of 10 m and an average trunk size smaller than an average trunk size of the first layer component is present in the first layer, the second layer, and the third layer other than the first layer component.

A mesoporous isoporous asymmetric material includes at least one diblock or multiblock copolymer, wherein the material has a transition layer having a thickness of at least 300 nm and a low macrovoid density, and the material has a sub-structure adjacent to said transition layer and said sub-structure comprises a high macrovoid density. A method for producing mesoporous isoporous asymmetric materials having macrovoids can include: dissolving at least one diblock or multiblock copolymer in a solution, the solution having one or more solvents and one or more nonsolvents, to form a polymer solution; dispensing the polymer solution onto a substrate or mold, or through a die or template; removing at least a portion of solvent and/or nonsolvent from the polymer solution to form a concentrated polymer solution; and exposing the concentrated polymer solution to a nonsolvent causing precipitation of at (least a portion of the polymer from the concentrated polymer solution.

A manufacturing method for an acidic gas separation membrane sheet includes: a step of preparing a hydrophilic resin composition liquid for forming a hydrophilic resin composition layer; a step of removing bubbles contained in the hydrophilic resin composition liquid; a step of applying the hydrophilic resin composition liquid onto a first porous layer to form an applied layer on the first porous layer; and a step of laminating a second porous layer on the applied layer to form a laminated body. The step of removing bubbles includes: a step of applying a shear to the hydrophilic resin composition liquid; and a step of leaving the hydrophilic resin composition liquid.

A manufacturing method for an acidic gas separation membrane sheet includes: a step of preparing a hydrophilic resin composition liquid for forming a hydrophilic resin composition layer; a step of removing bubbles contained in the hydrophilic resin composition liquid; a step of applying the hydrophilic resin composition liquid onto a first porous layer to form an applied layer on the first porous layer; and a step of laminating a second porous layer on the applied layer to form a laminated body. The step of removing bubbles includes: a step of applying a shear to the hydrophilic resin composition liquid; and a step of leaving the hydrophilic resin composition liquid.

Membranes, methods of making the membranes, and methods of using the membranes are described herein. The membranes can comprise a support layer, and a selective polymer layer disposed on the support layer. In some cases, the support layer can comprise a gas permeable polymer and hydrophilic additive dispersed within the gas permeable polymer. In some cases, the selective polymer layer can comprise a selective polymer matrix and carbon nanotubes dispersed within the selective polymer matrix. The membranes can exhibit selective permeability to gases. As such, the membranes can be for the selective removal of carbon dioxide and/or hydrogen sulfide from hydrogen and/or nitrogen.

A filtering device for obtaining a chemical liquid by purifying a liquid to be purified has an inlet portion, an outlet portion, a filter A, at least one filter B different from the filter A, and a flow path which includes the filter A and the filter B arranged in series between the inlet portion and the outlet portion and extends from the inlet portion to the outlet portion, in which the filter A has a porous base material made of polyfluorocarbon and a coating layer which is disposed to cover the porous base material and contains a first resin having a hydrophilic group.

Reverse osmosis (RO) separation of organic solvent mixtures where solvent molecular weights <100 Da is challenging especially for powerful solvents that swell most uncrosslinked polymers. To avoid polymer swelling by solvents, a particular perfluoropolymer, perfluoro-2,2-dimethyl-1,3-dioxole copolymerized with tetrafluoroethylene, (PDD-TFE), designated CMS-7, was studied. This amorphous glassy extremely hydrophobic copolymer has a very high free volume (FV) fraction. The maximum radial dimension of FV regions is less than 0.65 nm allowing only single solvent molecule permeation. Further, interactions between polarity, dimensions and shapes of solvent molecules with those of polymer FV elements can lead to extraordinarily selective permeation. Permeation behaviors of other solvent mixtures, toluene-n-heptane, NMP-tetrahydrofuran, methanol-water, ethanol-water as well as individual phases of the immiscible mixture of NMP and the nonpolar solvent n-heptane were also studied.

A process for recovering sulfur from a sour gas is provided. The process includes the steps of: providing the sour gas to a membrane separation unit having a carbon dioxide-selective membrane that comprises a perfluoropolymer, wherein the sour gas comprises carbon dioxide and at least 1 mol % hydrogen sulfide; separating the sour gas using the carbon dioxide-selective membrane in the membrane separation stage to obtain hydrogen sulfide-enriched gas and hydrogen sulfide-stripped gas, wherein the hydrogen sulfide-enriched gas has a hydrogen sulfide concentration of at least 20 mol %, and wherein the hydrogen sulfide-stripped gas comprises carbon dioxide; and processing the hydrogen sulfide-enriched gas in a sulfur recovery unit to obtain sulfur.

A process for recovering sulfur from a sour gas is provided. The process includes the steps of: providing the sour gas to a membrane separation unit having a carbon dioxide-selective membrane that comprises a perfluoropolymer, wherein the sour gas comprises carbon dioxide and at least 1 mol % hydrogen sulfide; separating the sour gas using the carbon dioxide-selective membrane in the membrane separation stage to obtain hydrogen sulfide-enriched gas and hydrogen sulfide-stripped gas, wherein the hydrogen sulfide-enriched gas has a hydrogen sulfide concentration of at least 20 mol %, and wherein the hydrogen sulfide-stripped gas comprises carbon dioxide; and processing the hydrogen sulfide-enriched gas in a sulfur recovery unit to obtain sulfur.