Embodiments described herein relate generally to systems, apparatus, and methods for using graphene oxide-containing membranes for separation and concentration processes. In some embodiments, a fluid component having a first concentration in a fluid mixture can be concentrated using a first distillation process to a second concentration. In some embodiments, the fluid component can be concentrated from the second concentration to a third concentration using a graphene oxide-containing membrane. In some embodiments, the fluid component can be concentrated from the third concentration to a fourth concentration using a second distillation process. In some embodiments, the fluid component can have an azeotropic concentration between the second concentration and the third concentration.

A method for making a titania-polymer nanocomposite by simultaneously forming TiO.sub.2 nanoparticles in situ from a TiO.sub.2 precursor in the presence of urea and interfacially polymerizing polyamide precursors thereby producing a titania-polymer nanocomposite. A titania-polymer nanocomposite made by this method. A method for removing a dye or metal from water comprising contacting contaminated water with the titania-polymer nanocomposite.

Methods and systems for the separation of hydrogen isotopes from one another are described. Methods include utilization of a hydrogen isotope selective separation membrane that includes a hydrogen isotope selective layer (e.g., graphene) and a hydrogen ion conductive supporting layer. An electronic driving force encourages passage of isotopes selectively across the membrane at an elevated separation temperature to enrich the product in a selected hydrogen isotope.

Described herein are nanofibers and methods for making nanofibers that include any one or more of (a) a non-homogeneous charge density; (b) a plurality of regions of high charge density; and/or (c) charged nanoparticles or chargeable nanoparticles. In one aspect, the present invention fulfills a need for filtration media that are capable of both high performance (e.g., removal of particle sizes between 0.1 and 0.5 μm) with a low pressure drop, however the invention is not limited in this regard.

Described herein is a technology for the creation of “smooth” metal oxide films or coatings using organic cross-linking agents to enable low-temperature sintering. These metal oxide films can be used in conjunction with low-melting temperature substrates, such as plastics, metal, metal oxide, and glass, providing exquisite control over surface roughness.

The present disclosure is directed to affinity chromatography devices including a fibrillated polymer membrane that contains inorganic particles having a spherical shape and a particle size distribution that has a D90/D10 less than or equal to 3. A blend or a combination of spherical inorganic particles may be utilized. A nominal particle size of the spherical inorganic particles is from about 5 microns to about 20 microns. An affinity ligand may be bonded to the spherical inorganic particles and/or to the fibrillated polymer membrane. Also, the affinity chromatography devices have a hydraulic permeability from about 100 (×10.sup.−12 cm.sup.2) to about 500 (×10.sup.−12 cm.sup.2). Additionally, the affinity chromatography devices have a cycling durability of at least 100 cycles without exceeding an pressure of 0.3 MPa. Manifolds containing multiple affinity chromatography devices in a parallel configuration and multiple manifolds in a parallel configuration are also disclosed.

The present specification discloses a membrane reactor comprising a reaction region; a permeate region; and a composite membrane disposed at a boundary of the reaction region and the permeate region, wherein the reaction region comprises a bed filled with a catalyst for dehydrogenation reaction, wherein the composite membrane comprises a support layer including a metal with a body-centered-cubic (BCC) crystal structure, and a catalyst layer including a palladium (Pd) or a palladium alloy formed onto the support layer, wherein ammonia (NH.sub.3) is supplied to the reaction region, the ammonia is converted into hydrogen (H.sub.2) by the dehydrogenation reaction in the presence of the catalyst for dehydrogenation reaction, and the hydrogen permeates the composite membrane and is emitted from the membrane reactor through the permeate region.

Provided is a method of producing a composite membrane in the form of laminated membranes in which a plurality of isoporous membranes are laminated, wherein the plurality of membranes laminated have through-holes having different sizes from each other and each membrane have the through-holes having the same size.

A method of manufacturing a PVDF composite separation membrane according to an embodiment of the present disclosure has advantages in that it is possible to control the size of pores in various ways based on the nonsolvent-induced phase transition process and calcination process, and manufacture a porous high-strength PVDF composite separation membrane having high water permeability, and it is possible to manufacture a PVDF composite separation membrane which may exhibit durability that does not damage the membrane even under high pressure, while having heat resistance applicable even at a high temperature of 150° C., and excellent chemical resistance to acids and alkalis, and suppress heavy metal adsorption and biofouling phenomenon, and may allow an organic material to be decomposed by ultrasonic waves or UV photocatalysts. In addition, the PVDF composite separation membrane has excellent mechanical, thermal and chemical resistance properties, suppresses the biofouling phenomenon, and exhibits high ultrasonic reactivity.

A method for making a titania-polymer nanocomposite by simultaneously forming TiO.sub.2 nanoparticles in situ from a TiO.sub.2 precursor in the presence of urea and interfacially polymerizing polyamide precursors thereby producing a titania-polymer nanocomposite. A titania-polymer nanocomposite made by this method. A method for removing a dye or metal from water comprising contacting contaminated water with the titania-polymer nanocomposite.