A process for producing a zeolite membrane composite includes a step of obtaining FAU-type seed crystals, a step of depositing the FAU-type seed crystals on a support, a step of forming an AFX-type zeolite membrane on the support by immersing the support in a raw material solution and growing an AFX-type zeolite from the FAU-type seed crystals by hydrothermal synthesis, and a step of removing a structure-directing agent from the AFX-type zeolite membrane. In this way, the AFX-type zeolite membrane can be provided.

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. The selective polymer layer can comprise an oxidatively stable carrier and a borate additive dispersed within a hydrophilic polymer matrix. The oxidatively stable carrier can comprise a quaternaryammonium hydroxide carrier (e.g., a mobile carrier such as a small molecule quaternaryammonium hydroxide, or a fixed carrier such as a quaternaryammonium hydroxide-containing polymer), a quaternaryammonium fluoride carrier (e.g., a mobile carrier such as a small molecule quaternaryammonium fluoride, or a fixed carrier such as a quaternaryammonium fluoride-containing polymer), or a combination thereof. The borate additive can comprise a borate salt, a boric acid, or a combination thereof. 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.

The present invention provides a carbon membrane for fluid separation that can suppress the breakage of a carbon membrane installed in a separation module during a vacuum desorption step before permeation of a fluid or during permeation of a fluid. The present invention provides a carbon membrane for fluid separation including a porous carbon support and a dense carbon layer provided on the porous carbon support, wherein the porous carbon support has an R.sub.s value of 1.0 or less, where the R.sub.s value is an R value (peak intensity of D-band (1360 cm.sup.−1)/peak intensity of G-band (1580 cm.sup.−1)) calculated from a Raman spectrum.

In one aspect, the invention provides a protein capture membrane comprising a first side and a second side and a plurality of interstices extending contiguously from the first side to the second side, wherein the interstices are coated with a protein-reactive coating; and the porous substrate comprises nanoporous alumina or porous glass. In another aspect the invention provides a method of detecting a protein of interest in a plurality of proteins.

A method of synthesis for an aluminophosphate-based zeolite membrane includes a steps of preparing a mixed solution with a pH greater than or equal to 6 and less than or equal to 9 by mixing an acidic phosphorous source with an alkali source, a steps of preparing a starting material solution by adding and mixing an aluminum source to the prepared mixed solution, and a steps of synthesizing an aluminophosphate-based zeolite membrane by hydrothermally synthesizing the starting material solution.

A method for preparing a super-hydrophobic membrane by cleaning a metal mesh by immersion in an organic solvent; subjecting the cleaned metal mesh to a surface modification treatment to increase its hydrophilicity; coating the treated metal mesh with a hydrophobic organic substance; and drying the metal coated mesh for obtaining the super-hydrophobic membrane. The super-hydrophobic membrane obtained thereby.

A solar membrane distillation apparatus includes a housing comprising a light transmitting wall. A solar distillation membrane is positioned in the housing to receive solar radiation transmitted through the light transmitting wall. The solar distillation membrane includes a porous graphitic foam and a coating of a hydrophobic composition on the surface and pores of the graphitic foam. A water chamber within the housing is provided for retaining water adjacent to the solar distillation membrane. A vapor chamber is provided for collecting water vapor distilling through the solar distillation membrane. A condenser is provided for condensing distilled water vapor from the vapor chamber into liquid water. A separation membrane and a method of solar distillation are also disclosed.

A membrane device is presented that can used for a wide range of applications from once-through filtration, crossflow filtration, molecular separation, gas/liquid absorption or reaction, gas dispersion into liquid, and degassing of liquid. The device comprises a thin flat sheet membrane that allows certain fluid or molecules go through while blocking others. The membrane sheet is fixed on a supporting structure with mini channel on two sides of the membrane for respective feed and sweep flows. The membrane sheet is sealed with gaskets with two cover plates that the membrane sheet can be replaced or cleaned. The cover plate provides connection ports to connect the feed fluid to the feed channels on one membrane surface and to connect the sweep fluid to the sweep channels on the other surface of the membrane.

A separation membrane complex includes a porous support, an intermediate membrane which is a polycrystalline membrane formed on a surface of the support and has pores that are originated from a framework structure and have an average pore diameter smaller than that of pores in the vicinity of the surface of the support, and a separation membrane which is formed on the intermediate membrane and is an inorganic membrane having a regular pore structure. In the separation membrane, a functional group is introduced into pores of a surface layer thereof which is away from the intermediate membrane.

The present invention relates to a method of controlling a defect structure in a chabazite (CHA) zeolite membrane, the CHA zeolite membrane having a controlled defect structure by the method and a method of separating CO.sub.2, H.sub.2, or He and water from a mixture of water and an organic solvent using the CHA zeolite membrane, and more particularly, to a method of controlling a defect structure in a CHA zeolite membrane that improves the separation performance by reducing the amount and size of defects formed in the CHA membrane structure when removing organic-structure-directing agents in the membrane through calcination at a low temperature using ozone.